WorldWideScience

Sample records for oceanic carbon uptake

  1. Ocean uptake of carbon dioxide

    International Nuclear Information System (INIS)

    Peng, Tsung-Hung; Takahashi, Taro

    1993-01-01

    Factors controlling the capacity of the ocean for taking up anthropogenic C0 2 include carbon chemistry, distribution of alkalinity, pCO 2 and total concentration of dissolved C0 2 , sea-air pCO 2 difference, gas exchange rate across the sea-air interface, biological carbon pump, ocean water circulation and mixing, and dissolution of carbonate in deep sea sediments. A general review of these processes is given and models of ocean-atmosphere system based on our understanding of these regulating processes axe used to estimate the magnitude of C0 2 uptake by the ocean. We conclude that the ocean can absorb up to 35% of the fossil fuel emission. Direct measurements show that 55% Of C0 2 from fossil fuel burning remains in the atmosphere. The remaining 10% is not accounted for by atmospheric increases and ocean uptake. In addition, it is estimated that an amount equivalent to 30% of recent annual fossil fuel emissions is released into the atmosphere as a result of deforestation and farming. To balance global carbon budget, a sizable carbon sink besides the ocean is needed. Storage of carbon in terrestrial biosphere as a result of C0 2 fertilization is a potential candidate for such missing carbon sinks

  2. Ocean carbon uptake and storage

    International Nuclear Information System (INIS)

    Tilbrook, Bronte

    2007-01-01

    Full text: The ocean contains about 95% of the carbon in the atmosphere, ocean and land biosphere system, and is of fundamental importance in regulating atmospheric carbon dioxide concentrations. In the 1990s an international research effort involving Australia was established to determine the uptake and storage of anthropogenic C02 for all major ocean basins. The research showed that about 118 of the 244 + 20 billion tons of the anthropogenic carbon emitted through fossil fuel burning and cement production has been stored in the ocean since preindustrial times, thus helping reduce the rate of increase in atmospheric C02. The research also showed the terrestrial biosphere has been a small net source of C02 (39 ± 28 billion tons carbon) to the atmosphere over the same period. About 60% of the total ocean inventory of the anthropogenic C02 was found in the Southern Hemisphere, with most in the 30 0 S to 50 0 S latitude band. This mid-latitude band is where surface waters are subducted as Mode and Intermediate waters, which is a major pathway controlling ocean C02 uptake. High storage (23% of the total) also occurs in the North Atlantic, associated with deep water formation in that basin. The ocean uptake and storage is expected to increase in the coming decades as atmospheric C02 concentrations rise. However, a number of feedback mechanisms associated with surface warming, changes in circulation, and biological effects are likely to impact on the uptake capacity. The accumulation or storage-of the C02 in the ocean is also the major driver of ocean acidification with potential to disrupt marine ecosystems. This talk will describe the current understanding of the ocean C02 uptake and storage and a new international research strategy to detect how the ocean uptake and storage will evolve on interannual through decadal scales. Understanding the ocean response to increasing atmospheric C02 will be a key element in managing future C02 increases and establishing

  3. Revised budget for the oceanic uptake of anthropogenic carbon dioxide

    Science.gov (United States)

    Sarmiento, J.L.; Sundquist, E.T.

    1992-01-01

    TRACER-CALIBRATED models of the total uptake of anthropogenic CO2 by the world's oceans give estimates of about 2 gigatonnes carbon per year1, significantly larger than a recent estimate2 of 0.3-0.8 Gt C yr-1 for the synoptic air-to-sea CO2 influx. Although both estimates require that the global CO2 budget must be balanced by a large unknown terrestrial sink, the latter estimate implies a much larger terrestrial sink, and challenges the ocean model calculations on which previous CO2 budgets were based. The discrepancy is due in part to the net flux of carbon to the ocean by rivers and rain, which must be added to the synoptic air-to-sea CO2 flux to obtain the total oceanic uptake of anthropogenic CO2. Here we estimate the magnitude of this correction and of several other recently proposed adjustments to the synoptic air-sea CO2 exchange. These combined adjustments minimize the apparent inconsistency, and restore estimates of the terrestrial sink to values implied by the modelled oceanic uptake.

  4. Global ocean carbon uptake: magnitude, variability and trends

    Directory of Open Access Journals (Sweden)

    R. Wanninkhof

    2013-03-01

    Full Text Available The globally integrated sea–air anthropogenic carbon dioxide (CO2 flux from 1990 to 2009 is determined from models and data-based approaches as part of the Regional Carbon Cycle Assessment and Processes (RECCAP project. Numerical methods include ocean inverse models, atmospheric inverse models, and ocean general circulation models with parameterized biogeochemistry (OBGCMs. The median value of different approaches shows good agreement in average uptake. The best estimate of anthropogenic CO2 uptake for the time period based on a compilation of approaches is −2.0 Pg C yr−1. The interannual variability in the sea–air flux is largely driven by large-scale climate re-organizations and is estimated at 0.2 Pg C yr−1 for the two decades with some systematic differences between approaches. The largest differences between approaches are seen in the decadal trends. The trends range from −0.13 (Pg C yr−1 decade−1 to −0.50 (Pg C yr−1 decade−1 for the two decades under investigation. The OBGCMs and the data-based sea–air CO2 flux estimates show appreciably smaller decadal trends than estimates based on changes in carbon inventory suggesting that methods capable of resolving shorter timescales are showing a slowing of the rate of ocean CO2 uptake. RECCAP model outputs for five decades show similar differences in trends between approaches.

  5. On the relations between the oceanic uptake of CO2 and its carbon isotopes

    International Nuclear Information System (INIS)

    Heimann, M.; Maier-Reimer, E.

    1994-01-01

    The recent proposals to estimate the oceanic uptake of CO 2 by monitoring the oceanic change in 13 C/ 12 C isotope ratio or the air-sea 13 C/ 12 C isotopic disequilibrium is reviewed. Because the history of atmospheric CO 2 and 13 CO 2 since preindustrial times is almost the same, the oceanic penetration depth of both tracers must be the same. This dynamic constraint permits the establishment of yet a third method to estimate the global ocean uptake of CO 2 from 13 C measurements. Using available observations in conjunction with canonical values for the global carbon cycle parameters the three methods yield inconsistent oceanic CO 2 uptake rates for the time period 1970-1990, ranging from 0 to over 3 GtC year -1 . However, uncertainties in the available carbon cycle data must be taken into account. Using a non-linear estimation procedure, a consistent scenario with an oceanic CO 2 uptake rate of 2.2±0.8 GtC year -1 can be established. The method also permits an investigation of the sensitivities of the different approaches. An analysis of the results of two three-dimensional simulations with the Hamburg Model of the Oceanic Carbon Cycle shows that the 13 C isotope indeed tracks the oceanic penetration of anthropogenic CO 2 . Because of its different time history, bomb produced radiocarbon, as measured at the time of GEOSECS, correlates much less well to excess carbon. (orig.)

  6. Increase in observed net carbon dioxide uptake by land and oceans during the past 50 years.

    Science.gov (United States)

    Ballantyne, A P; Alden, C B; Miller, J B; Tans, P P; White, J W C

    2012-08-02

    One of the greatest sources of uncertainty for future climate predictions is the response of the global carbon cycle to climate change. Although approximately one-half of total CO(2) emissions is at present taken up by combined land and ocean carbon reservoirs, models predict a decline in future carbon uptake by these reservoirs, resulting in a positive carbon-climate feedback. Several recent studies suggest that rates of carbon uptake by the land and ocean have remained constant or declined in recent decades. Other work, however, has called into question the reported decline. Here we use global-scale atmospheric CO(2) measurements, CO(2) emission inventories and their full range of uncertainties to calculate changes in global CO(2) sources and sinks during the past 50 years. Our mass balance analysis shows that net global carbon uptake has increased significantly by about 0.05 billion tonnes of carbon per year and that global carbon uptake doubled, from 2.4 ± 0.8 to 5.0 ± 0.9 billion tonnes per year, between 1960 and 2010. Therefore, it is very unlikely that both land and ocean carbon sinks have decreased on a global scale. Since 1959, approximately 350 billion tonnes of carbon have been emitted by humans to the atmosphere, of which about 55 per cent has moved into the land and oceans. Thus, identifying the mechanisms and locations responsible for increasing global carbon uptake remains a critical challenge in constraining the modern global carbon budget and predicting future carbon-climate interactions.

  7. Global and regional ocean carbon uptake and climate change: sensitivity to a substantial mitigation scenario

    Energy Technology Data Exchange (ETDEWEB)

    Vichi, Marcello; Masina, Simona; Navarra, Antonio [Centro Euro-Mediterraneo per i Cambiamenti Climatici (CMCC), Bologna (Italy); Istituto Nazionale di Geofisica e Vulcanologia, Bologna (Italy); Manzini, Elisa [Centro Euro-Mediterraneo per i Cambiamenti Climatici (CMCC), Bologna (Italy); Istituto Nazionale di Geofisica e Vulcanologia, Bologna (Italy); Max Planck Institute for Meteorology, Hamburg (Germany); Fogli, Pier Giuseppe [Centro Euro-Mediterraneo per i Cambiamenti Climatici (CMCC), Bologna (Italy); Alessandri, Andrea [Centro Euro-Mediterraneo per i Cambiamenti Climatici (CMCC), Bologna (Italy); ENEA, Rome (Italy); Patara, Lavinia [Centro Euro-Mediterraneo per i Cambiamenti Climatici (CMCC), Bologna (Italy); Leibniz Institute of Marine Sciences (IFM-GEOMAR), Kiel (Germany); Scoccimarro, Enrico [Istituto Nazionale di Geofisica e Vulcanologia, Bologna (Italy)

    2011-11-15

    Under future scenarios of business-as-usual emissions, the ocean storage of anthropogenic carbon is anticipated to decrease because of ocean chemistry constraints and positive feedbacks in the carbon-climate dynamics, whereas it is still unknown how the oceanic carbon cycle will respond to more substantial mitigation scenarios. To evaluate the natural system response to prescribed atmospheric ''target'' concentrations and assess the response of the ocean carbon pool to these values, 2 centennial projection simulations have been performed with an Earth System Model that includes a fully coupled carbon cycle, forced in one case with a mitigation scenario and the other with the SRES A1B scenario. End of century ocean uptake with the mitigation scenario is projected to return to the same magnitude of carbon fluxes as simulated in 1960 in the Pacific Ocean and to lower values in the Atlantic. With A1B, the major ocean basins are instead projected to decrease the capacity for carbon uptake globally as found with simpler carbon cycle models, while at the regional level the response is contrasting. The model indicates that the equatorial Pacific may increase the carbon uptake rates in both scenarios, owing to enhancement of the biological carbon pump evidenced by an increase in Net Community Production (NCP) following changes in the subsurface equatorial circulation and enhanced iron availability from extratropical regions. NCP is a proxy of the bulk organic carbon made available to the higher trophic levels and potentially exportable from the surface layers. The model results indicate that, besides the localized increase in the equatorial Pacific, the NCP of lower trophic levels in the northern Pacific and Atlantic oceans is projected to be halved with respect to the current climate under a substantial mitigation scenario at the end of the twenty-first century. It is thus suggested that changes due to cumulative carbon emissions up to present and the

  8. Ocean Heat and Carbon Uptake in Transient Climate Change: Identifying Model Uncertainty

    Science.gov (United States)

    Romanou, Anastasia; Marshall, John

    2015-01-01

    Global warming on decadal and centennial timescales is mediated and ameliorated by the oceansequestering heat and carbon into its interior. Transient climate change is a function of the efficiency by whichanthropogenic heat and carbon are transported away from the surface into the ocean interior (Hansen et al. 1985).Gregory and Mitchell (1997) and Raper et al. (2002) were the first to identify the importance of the ocean heat uptakeefficiency in transient climate change. Observational estimates (Schwartz 2012) and inferences from coupledatmosphere-ocean general circulation models (AOGCMs; Gregory and Forster 2008; Marotzke et al. 2015), suggest thatocean heat uptake efficiency on decadal timescales lies in the range 0.5-1.5 W/sq m/K and is thus comparable to theclimate feedback parameter (Murphy et al. 2009). Moreover, the ocean not only plays a key role in setting the timing ofwarming but also its regional patterns (Marshall et al. 2014), which is crucial to our understanding of regional climate,carbon and heat uptake, and sea-level change. This short communication is based on a presentation given by A.Romanou at a recent workshop, Oceans Carbon and Heat Uptake: Uncertainties and Metrics, co-hosted by US CLIVARand OCB. As briefly reviewed below, we have incomplete but growing knowledge of how ocean models used in climatechange projections sequester heat and carbon into the interior. To understand and thence reduce errors and biases inthe ocean component of coupled models, as well as elucidate the key mechanisms at work, in the final section we outlinea proposed model intercomparison project named FAFMIP. In FAFMIP, coupled integrations would be carried out withprescribed overrides of wind stress and freshwater and heat fluxes acting at the sea surface.

  9. Uptake by the Atlantic Ocean of excess atmospheric carbon dioxide and radiocarbon

    International Nuclear Information System (INIS)

    Bolin, B.; Bjorkstrom, A.

    1989-01-01

    Inverse methods have been used to deduce water circulation, spatial patterns of turbulent exchange and biological activity in the Atlantic Ocean, by using a set of stationary tracers and a condition of quasi-geostrophic flow. The solution yields a direct meridional circulation cell with descending motion in the northern Atlantic with an intensity of 20-25 Sverdrup, a reasonable distribution of vertical turbulent transfer in the uppermost ocean layers and comparatively large rates of detritus formation, about 4.5 Pg C yr -1 . The solution is used to compute the invasion of tritium 1955-1983, and the uptake of excess radiocarbon and carbon dioxide during the period 1760-1983. A fair agreement between computed and observed changes of tritium and 14 C is obtained, but the period of observations is too short to serve as a conclusive test model. The uptake of carbon dioxide during the 220 years period into the Atlantic Ocean is 33 ± 5 Pg and it is further found that significant variations of the uptake fraction of the CO 2 emissions may have occurred due to varying rates of emissions in gorce of time. The conclusion is drawn that the ocean and its carbonate system may not have been the only sink for anthropogenic emissions of carbon dioxide into the atmosphere. Means for how to further improve the model and its capability to reproduce the ocean behaviour are discussed. Burning of fossil fuels, deforestation and changing land use have changed the global carbon cycle very significant during the last two centuries

  10. Current and Future Decadal Trends in the Oceanic Carbon Uptake Are Dominated by Internal Variability

    Science.gov (United States)

    Li, Hongmei; Ilyina, Tatiana

    2018-01-01

    We investigate the internal decadal variability of the ocean carbon uptake using 100 ensemble simulations based on the Max Planck Institute Earth system model (MPI-ESM). We find that on decadal time scales, internal variability (ensemble spread) is as large as the forced temporal variability (ensemble mean), and the largest internal variability is found in major carbon sink regions, that is, the 50-65°S band of the Southern Ocean, the North Pacific, and the North Atlantic. The MPI-ESM ensemble produces both positive and negative 10 year trends in the ocean carbon uptake in agreement with observational estimates. Negative decadal trends are projected to occur in the future under RCP4.5 scenario. Due to the large internal variability, the Southern Ocean and the North Pacific require the most ensemble members (more than 53 and 46, respectively) to reproduce the forced decadal trends. This number increases up to 79 in future decades as CO2 emission trajectory changes.

  11. Role of ocean isopycnal mixing in setting the uptake of anthropogenic carbon

    Science.gov (United States)

    Gnanadesikan, A.; Pradal, M. A. S.; Abernathey, R. P.

    2014-12-01

    The magnitude of the isopycnal stirring coefficient ARedi is poorly constrained from data and varies greatly across Earth System Models. This paper documents the impact of such uncertainty on the oceanic carbon cycle. We compare six spatial representations of ARedi. Four constant values (400, 800, 1200 and 2400 m2/s) are used to explore the difference between using the low values found in many models and the higher values seen in observational estimates. Models are also run with two spatially dependent values of ARedi based on altimetry, one which captures the fully two-dimensional structure of the mixing coefficient, the other of which looks at the zonally averaged structure alone. Under global warming significant changes are seen in the biological pump in convective regions, but these changes are largely locally compensated by changes in preformed DIC. Instead, differences in anthropogenic uptake of carbon are largely centered in the tropics, and can be well described in terms of a relatively simple diffusive approximation. Using ideal age as a tracer can give insight into the expected behavior of the models. The rate of oceanic mixing represents a quantitatively significant uncertainty in future projections of the global carbon cycle, amounting to about 20% of the oceanic uptake.

  12. Detecting the anthropogenic influences on recent changes in ocean carbon uptake

    International Nuclear Information System (INIS)

    Seferian, Roland; Ribes, Aurelien; Bopp, Laurent

    2014-01-01

    Anthropogenic greenhouse gas emissions have modified the rate at which oceans have absorbed atmospheric CO 2 over the last centuries through rising atmospheric CO 2 and modifications in climate. However, there are still missing pieces in our understanding of the recent evolution of air-sea CO 2 exchanges related to the magnitude of their response to anthropogenic forcing versus that controlled by the internal variability. Here, to detect and attribute anthropogenic influences on oceanic CO 2 uptake between 1960 and 2005, we compare an ensemble of Coupled Model Intercomparison Project Phase 5 (CMIP5) climate model simulations forced by individual drivers to ocean-only model reconstructions. We demonstrate that the evolution of the global oceanic carbon sink over the last decades can be understood without invoking climate change, attributing rising atmospheric CO 2 as prominent driver of the oceanic sink. Nonetheless, at regional scale, the influence of climate change on air-sea CO 2 exchanges seems to emerge from the internal variability within the low-latitude oceans. (authors)

  13. Isopycnal mixing by mesoscale eddies significantly impacts oceanic anthropogenic carbon uptake

    Science.gov (United States)

    Gnanadesikan, Anand; Pradal, Marie-Aude; Abernathey, Ryan

    2015-06-01

    Anthropogenic carbon dioxide uptake varies across Earth System Models for reasons that have remained obscure. When varied within a single model, the lateral eddy mixing coefficient ARedi produces a range of uptake similar to the modeled range. The highest uptake, resulting from a simulation with a constant ARedi of 2400 m2/s, simulates 15% more historical carbon uptake than a model with ARedi = 400 m2/s. A sudden doubling in carbon dioxide produces a 21% range in carbon uptake across the models. Two spatially dependent representations of ARedi produce uptake that lies in the middle of the range of constant values despite predicting very large values in the subtropical gyres. One-dimensional diffusive models of the type used for integrated assessments can be fit to the simulations, with ARedi accounting for a substantial fraction of the effective vertical diffusion. Such models, however, mask significant regional changes in stratification and biological carbon storage.

  14. Regional impacts of climate change and atmospheric CO2 on future ocean carbon uptake: a multi model linear feedback analysis

    International Nuclear Information System (INIS)

    Roy, Tilla; Bopp, Laurent; Gehlen, Marion; Cadule, Patricia; Schneider, Birgit; Frolicher, Thomas L.; Segschneider, Joachim; Tjiputra, Jerry; Heinze, Christoph; Joos, Fortunat

    2011-01-01

    The increase in atmospheric CO 2 over this century depends on the evolution of the oceanic air-sea CO 2 uptake, which will be driven by the combined response to rising atmospheric CO 2 itself and climate change. Here, the future oceanic CO 2 uptake is simulated using an ensemble of coupled climate-carbon cycle models. The models are driven by CO 2 emissions from historical data and the Special Report on Emissions Scenarios (SRES) A2 high-emission scenario. A linear feedback analysis successfully separates the regional future (2010-2100) oceanic CO 2 uptake into a CO 2 -induced component, due to rising atmospheric CO 2 concentrations, and a climate-induced component, due to global warming. The models capture the observation based magnitude and distribution of anthropogenic CO 2 uptake. The distributions of the climate-induced component are broadly consistent between the models, with reduced CO 2 uptake in the sub polar Southern Ocean and the equatorial regions, owing to decreased CO 2 solubility; and reduced CO 2 uptake in the mid-latitudes, owing to decreased CO 2 solubility and increased vertical stratification. The magnitude of the climate-induced component is sensitive to local warming in the southern extra-tropics, to large freshwater fluxes in the extra-tropical North Atlantic Ocean, and to small changes in the CO 2 solubility in the equatorial regions. In key anthropogenic CO 2 uptake regions, the climate-induced component offsets the CO 2 - induced component at a constant proportion up until the end of this century. This amounts to approximately 50% in the northern extra-tropics and 25% in the southern extra-tropics and equatorial regions. Consequently, the detection of climate change impacts on anthropogenic CO 2 uptake may be difficult without monitoring additional tracers, such as oxygen. (authors)

  15. Regional impacts of climate change and atmospheric CO2 on future ocean carbon uptake: a multi model linear feedback analysis

    International Nuclear Information System (INIS)

    Roy, Tilla; Bopp, Laurent; Gehlen, Marion; Cadule, Patricia

    2011-01-01

    The increase in atmospheric CO 2 over this century depends on the evolution of the oceanic air-sea CO 2 uptake, which will be driven by the combined response to rising atmospheric CO 2 itself and climate change. Here, the future oceanic CO 2 uptake is simulated using an ensemble of coupled climate-carbon cycle models. The models are driven by CO 2 emissions from historical data and the Special Report on Emissions Scenarios (SRES) A2 high-emission scenario. A linear feedback analysis successfully separates the regional future (2010-2100) oceanic CO 2 uptake into a CO 2 -induced component, due to rising atmospheric CO 2 concentrations, and a climate-induced component, due to global warming. The models capture the observation based magnitude and distribution of anthropogenic CO 2 uptake. The distributions of the climate-induced component are broadly consistent between the models, with reduced CO 2 uptake in the sub-polar Southern Ocean and the equatorial regions, owing to decreased CO 2 solubility; and reduced CO 2 uptake in the mid latitudes, owing to decreased CO 2 solubility and increased vertical stratification. The magnitude of the climate-induced component is sensitive to local warming in the southern extra tropics, to large freshwater fluxes in the extra tropical North Atlantic Ocean, and to small changes in the CO 2 solubility in the equatorial regions. In key anthropogenic CO 2 uptake regions, the climate-induced component offsets the CO 2 - induced component at a constant proportion up until the end of this century. This amounts to approximately 50% in the northern extra tropics and 25% in the southern extra tropics and equatorial regions. Consequently, the detection of climate change impacts on anthropogenic CO 2 uptake may be difficult without monitoring additional tracers, such as oxygen. (authors)

  16. The Impact of Variable Phytoplankton Stoichiometry on Projections of Primary Production, Food Quality, and Carbon Uptake in the Global Ocean

    Science.gov (United States)

    Kwiatkowski, Lester; Aumont, Olivier; Bopp, Laurent; Ciais, Philippe

    2018-04-01

    Ocean biogeochemical models are integral components of Earth system models used to project the evolution of the ocean carbon sink, as well as potential changes in the physical and chemical environment of marine ecosystems. In such models the stoichiometry of phytoplankton C:N:P is typically fixed at the Redfield ratio. The observed stoichiometry of phytoplankton, however, has been shown to considerably vary from Redfield values due to plasticity in the expression of phytoplankton cell structures with different elemental compositions. The intrinsic structure of fixed C:N:P models therefore has the potential to bias projections of the marine response to climate change. We assess the importance of variable stoichiometry on 21st century projections of net primary production, food quality, and ocean carbon uptake using the recently developed Pelagic Interactions Scheme for Carbon and Ecosystem Studies Quota (PISCES-QUOTA) ocean biogeochemistry model. The model simulates variable phytoplankton C:N:P stoichiometry and was run under historical and business-as-usual scenario forcing from 1850 to 2100. PISCES-QUOTA projects similar 21st century global net primary production decline (7.7%) to current generation fixed stoichiometry models. Global phytoplankton N and P content or food quality is projected to decline by 1.2% and 6.4% over the 21st century, respectively. The largest reductions in food quality are in the oligotrophic subtropical gyres and Arctic Ocean where declines by the end of the century can exceed 20%. Using the change in the carbon export efficiency in PISCES-QUOTA, we estimate that fixed stoichiometry models may be underestimating 21st century cumulative ocean carbon uptake by 0.5-3.5% (2.0-15.1 PgC).

  17. Marine ecosystem community carbon and nutrient uptake stoichiometry under varying ocean acidification during the PeECE III experiment

    Directory of Open Access Journals (Sweden)

    R. G. J. Bellerby

    2008-11-01

    Full Text Available Changes to seawater inorganic carbon and nutrient concentrations in response to the deliberate CO2 perturbation of natural plankton assemblages were studied during the 2005 Pelagic Ecosystem CO2 Enrichment (PeECE III experiment. Inverse analysis of the temporal inorganic carbon dioxide system and nutrient variations was used to determine the net community stoichiometric uptake characteristics of a natural pelagic ecosystem perturbed over a range of pCO2 scenarios (350, 700 and 1050 μatm. Nutrient uptake showed no sensitivity to CO2 treatment. There was enhanced carbon production relative to nutrient consumption in the higher CO2 treatments which was positively correlated with the initial CO2 concentration. There was no significant calcification response to changing CO2 in Emiliania huxleyi by the peak of the bloom and all treatments exhibited low particulate inorganic carbon production (~15 μmol kg−1. With insignificant air-sea CO2 exchange across the treatments, the enhanced carbon uptake was due to increase organic carbon production. The inferred cumulative C:N:P stoichiometry of organic production increased with CO2 treatment from 1:6.3:121 to 1:7.1:144 to 1:8.25:168 at the height of the bloom. This study discusses how ocean acidification may incur modification to the stoichiometry of pelagic production and have consequences for ocean biogeochemical cycling.

  18. Temporal evolution of mechanisms controlling ocean carbon uptake during the last glacial cycle

    Science.gov (United States)

    Kohfeld, Karen E.; Chase, Zanna

    2017-08-01

    Many mechanisms have been proposed to explain the ∼85-90 ppm decrease in atmospheric carbon dioxide (CO2) during the last glacial cycle, between 127,000 and 18,000 yrs ago. When taken together, these mechanisms can, in some models, account for the full glacial-interglacial CO2 drawdown. Most proxy-based evaluations focus on the peak of the Last Glacial Maximum, 24,000-18,000 yrs ago, and little has been done to determine the sequential timing of processes affecting CO2 during the last glacial cycle. Here we use a new compilation of sea-surface temperature records together with time-sequenced records of carbon and Nd isotopes, and other proxies to determine when the most commonly proposed mechanisms could have been important for CO2 drawdown. We find that the initial major drawdown of 35 ppm 115,000 yrs ago was most likely a result of Antarctic sea ice expansion. Importantly, changes in deep ocean circulation and mixing did not play a major role until at least 30,000 yrs after the first CO2 drawdown. The second phase of CO2 drawdown occurred ∼70,000 yrs ago and was also coincident with the first significant influences of enhanced ocean productivity due to dust. Finally, minimum concentrations of atmospheric CO2 during the Last Glacial Maximum resulted from the combination of physical and biological factors, including the barrier effect of expanded Southern Ocean sea ice, slower ventilation of the deep sea, and ocean biological feedbacks.

  19. In-situ Measured Carbon and Nitrogen Uptake Rates of Melt Pond Algae in the Western Arctic Ocean, 2014

    Science.gov (United States)

    Song, Ho Jung; Kim, Kwanwoo; Lee, Jae Hyung; Ahn, So Hyun; Joo, Houng-Min; Jeong, Jin Young; Yang, Eun Jin; Kang, Sung-Ho; Yun, Mi Sun; Lee, Sang Heon

    2018-03-01

    Although the areal coverage of melt pond in the Arctic Ocean has recently increased, very few biological researches have been conducted. The objectives in this study were to ascertain the uptake rates of carbon and nitrogen in various melt ponds and to understand the major controlling factors for the rates. We obtained 22 melt pond samples at ice camp 1 (146.17°W, 77.38°N) and 11 melt pond samples at ice camp 2 (169.79°W, 76.52°N). The major nutrient concentrations varied largely among melt ponds at the ice camps 1 and 2. The chl-a concentrations averaged from the melt ponds at camps 1 and 2 were 0.02-0.56 mg chl-a m-3 (0.12 ± 0.12 mg chl-a m-3) and 0.08-0.30 mg chl-a m-3 (0.16 ± 0.08 mg chl-a m-3), respectively. The hourly carbon uptake rates at camps 1 and 2 were 0.001-0.080 mg C m-3 h-1 (0.025 ± 0.024 mg C m-3 h-1) and 0.022-0.210 mg C m-3 h-1 (0.077 ± 0.006 mg C m-3 h-1), respectively. In comparison, the nitrogen uptake rates at camps 1 and 2 were 0.001-0.030 mg N m-3 h-1 (0.011 ± 0.010 mg N m-3 h-1) and 0.002-0.022 mg N m-3 h-1 (0.010 ± 0.006 mg N m-3 h-1), respectively. The values obtained in this study are significantly lower than those reported previously. A large portion of algal biomass trapped in the new forming surface ice in melt ponds appears to be one of the main potential reasons for the lower chl-a concentration and subsequently lower carbon and nitrogen uptake rates revealed in this study. A long-term monitoring program on melt ponds is needed to understand the response of the Arctic marine ecosystem to ongoing environmental changes.

  20. Regional impacts of climate change and atmospheric CO2 on future ocean carbon uptake: A multi-model linear feedback analysis

    OpenAIRE

    Roy Tilla; Bopp Laurent; Gehlen Marion; Schneider Birgitt; Cadule Patricia; Frölicher Thomas; Segschneider Jochen; Tijputra Jerry; Heinze Christoph; Joos Fortunat

    2011-01-01

    The increase in atmospheric CO2 over this century depends on the evolution of the oceanic air–sea CO2 uptake which will be driven by the combined response to rising atmospheric CO2 itself and climate change. Here the future oceanic CO2 uptake is simulated using an ensemble of coupled climate–carbon cycle models. The models are driven by CO2 emissions from historical data and the Special Report on Emissions Scenarios (SRES) A2 high emission scenario. A linear feedback analysis successfully sep...

  1. Spatial and temporal variability in nutrients and carbon uptake during 2004 and 2005 in the eastern equatorial Pacific Ocean

    DEFF Research Database (Denmark)

    Palacz, A. P.; Chai, F.

    2012-01-01

    The eastern equatorial Pacific plays a great role in the global carbon budget due to its enhanced biological productivity linked to the equatorial upwelling. However, as confirmed by the Equatorial Biocomplexity cruises in 2004 and 2005, nutrient upwelling supply varies strongly, partly due...... and intraseasonal time scales. Here, high resolution Pacific ROMS-CoSiNE (Regional Ocean Modeling System-Carbon, Silicon, Nitrogen Ecosystem) model results were evaluated with in situ and remote sensing data. The results of model-data comparison revealed a good agreement in domain-average hydrographic....... In order to fully resolve the complexity of biological and physical interactions in the eastern equatorial Pacific, we recommended improving CoSiNE and other models by introducing more phytoplankton groups, variable Redfield and carbon to chlorophyll ratios, as well as resolving the Fe-Si co...

  2. Process studies of the carbonate system in coastal and ocean environments of the Atlantic Ocean

    NARCIS (Netherlands)

    Salt, L.A.

    2014-01-01

    The increase in anthropogenic, atmospheric carbon dioxide (CO2) has been largely mitigated by ocean uptake since the start of the Industrial Revolution, with the Atlantic Ocean providing the largest store of anthropogenic carbon. The thesis of Lesley Salt examines how the uptake of CO2 varies in

  3. Ocean carbon sinks and international climate policy

    International Nuclear Information System (INIS)

    Rehdanz, Katrin; Tol, Richard S.J.; Wetzel, Patrick

    2006-01-01

    Terrestrial vegetation sinks have entered the Kyoto Protocol as offsets for anthropogenic greenhouse gas emissions, but ocean sinks have escaped attention. Ocean sinks are as unexplored and uncertain as were the terrestrial sinks at the time of negotiation of the Kyoto Protocol. It is not unlikely that certain countries will advocate the inclusion of ocean carbon sinks to reduce their emission reduction obligations in post-2012 negotiations. We use a simple model of the international market for carbon dioxide emissions to evaluate who would gain or loose from allowing for ocean carbon sinks. Our analysis is restricted to information on anthropogenic carbon sequestration within the exclusive economic zone of a country. We use information on the actual carbon flux and derive the human-induced uptake for the period from 1990 onwards. Like the carbon sequestration of business as usual forest management activities, natural ocean carbon sequestration applies at zero costs. The total amount of anthropogenic ocean carbon sequestration is large, also in the exclusive economic zones. As a consequence, it substantially alters the costs of emission reduction for most countries. Countries such as Australia, Denmark, France, Iceland, New Zealand, Norway and Portugal would gain substantially, and a large number of countries would benefit too. Current net exporters of carbon permits, particularly Russia, would gain less and oppose the inclusion of ocean carbon sinks

  4. The role of ocean transport in the uptake of anthropogenic CO2

    Directory of Open Access Journals (Sweden)

    I. Totterdell

    2009-03-01

    Full Text Available We compare modeled oceanic carbon uptake in response to pulse CO2 emissions using a suite of global ocean models and Earth system models. In response to a CO2 pulse emission of 590 Pg C (corresponding to an instantaneous doubling of atmospheric CO2 from 278 to 556 ppm, the fraction of CO2 emitted that is absorbed by the ocean is: 37±8%, 56±10%, and 81±4% (model mean ±2σ in year 30, 100, and 1000 after the emission pulse, respectively. Modeled oceanic uptake of pulse CO2 on timescales from decades to about a century is strongly correlated with simulated present-day uptake of chlorofluorocarbons (CFCs and CO2 across all models, while the amount of pulse CO2 absorbed by the ocean from a century to a millennium is strongly correlated with modeled radiocarbon in the deep Southern and Pacific Ocean. However, restricting the analysis to models that are capable of reproducing observations within uncertainty, the correlation is generally much weaker. The rates of surface-to-deep ocean transport are determined for individual models from the instantaneous doubling CO2 simulations, and they are used to calculate oceanic CO2 uptake in response to pulse CO2 emissions of different sizes pulses of 1000 and 5000 Pg C. These results are compared with simulated oceanic uptake of CO2 by a number of models simulations with the coupling of climate-ocean carbon cycle and without it. This comparison demonstrates that the impact of different ocean transport rates across models on oceanic uptake of anthropogenic CO2 is of similar magnitude as that of climate-carbon cycle feedbacks in a single model, emphasizing the important role of ocean transport in the uptake of anthropogenic CO2.

  5. Chromium isotope uptake in carbonates

    DEFF Research Database (Denmark)

    Rodler, Alexandra

    related to the rise of oxygen and the evolution of the biosphere. However, before the Cr isotopesystem can be applied to faithfully delineate paleo-environmental changes, careful assessment of the signal robustness and a thorough understanding of the Cr cycle in Earth system processes is necessary...... composition of contemporaneous seawater. Marine carbonates are ubiquitous throughout Earth’s rock record rendering them a particularly interesting archive for constraining past changes in ocean chemistry. This thesis includes an investigation of the fractionation behavior of Cr isotopesduring coprecipitation...

  6. Global Ocean Carbon and Biogeochemistry Coordination

    Science.gov (United States)

    Telszewski, Maciej; Tanhua, Toste; Palacz, Artur

    2016-04-01

    The complexity of the marine carbon cycle and its numerous connections to carbon's atmospheric and terrestrial pathways means that a wide range of approaches have to be used in order to establish it's qualitative and quantitative role in the global climate system. Ocean carbon and biogeochemistry research, observations, and modelling are conducted at national, regional, and global levels to quantify the global ocean uptake of atmospheric CO2 and to understand controls of this process, the variability of uptake and vulnerability of carbon fluxes into the ocean. These science activities require support by a sustained, international effort that provides a central communication forum and coordination services to facilitate the compatibility and comparability of results from individual efforts and development of the ocean carbon data products that can be integrated with the terrestrial, atmospheric and human dimensions components of the global carbon cycle. The International Ocean Carbon Coordination Project (IOCCP) was created in 2005 by the IOC of UNESCO and the Scientific Committee on Oceanic Research. IOCCP provides an international, program-independent forum for global coordination of ocean carbon and biogeochemistry observations and integration with global carbon cycle science programs. The IOCCP coordinates an ever-increasing set of observations-related activities in the following domains: underway observations of biogeochemical water properties, ocean interior observations, ship-based time-series observations, large-scale ocean acidification monitoring, inorganic nutrients observations, biogeochemical instruments and autonomous sensors and data and information creation. Our contribution is through the facilitation of the development of globally acceptable strategies, methodologies, practices and standards homogenizing efforts of the research community and scientific advisory groups as well as integrating the ocean biogeochemistry observations with the

  7. Impact of atmospheric and terrestrial CO2 feedbacks on fertilization-induced marine carbon uptake

    Science.gov (United States)

    Oschlies, A.

    2009-08-01

    The sensitivity of oceanic CO2 uptake to alterations in the marine biological carbon pump, such as brought about by natural or purposeful ocean fertilization, has repeatedly been investigated by studies employing numerical biogeochemical ocean models. It is shown here that the results of such ocean-centered studies are very sensitive to the assumption made about the response of the carbon reservoirs on the atmospheric side of the sea surface. Assumptions made include prescribed atmospheric pCO2, an interactive atmospheric CO2 pool exchanging carbon with the ocean but not with the terrestrial biosphere, and an interactive atmosphere that exchanges carbon with both oceanic and terrestrial carbon pools. The impact of these assumptions on simulated annual to millennial oceanic carbon uptake is investigated for a hypothetical increase in the C:N ratio of the biological pump and for an idealized enhancement of phytoplankton growth. Compared to simulations with interactive atmosphere, using prescribed atmospheric pCO2 overestimates the sensitivity of the oceanic CO2 uptake to changes in the biological pump, by about 2%, 25%, 100%, and >500% on annual, decadal, centennial, and millennial timescales, respectively. The smaller efficiency of the oceanic carbon uptake under an interactive atmosphere is due to the back flux of CO2 that occurs when atmospheric CO2 is reduced. Adding an interactive terrestrial carbon pool to the atmosphere-ocean model system has a small effect on annual timescales, but increases the simulated fertilization-induced oceanic carbon uptake by about 4%, 50%, and 100% on decadal, centennial, and millennial timescales, respectively, for pCO2 sensitivities of the terrestrial carbon storage in the middle range of the C4MIP models (Friedlingstein et al., 2006). For such sensitivities, a substantial fraction of oceanic carbon uptake induced by natural or purposeful ocean fertilization originates, on timescales longer than decades, not from the atmosphere

  8. The microbial fate of carbon in high-latitude seas: Impact of the microbial loop on oceanic uptake of CO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Yager, P.L.

    1996-12-31

    This dissertation examines pelagic microbial processes in high-latitude seas, how they affect regional and global carbon cycling, and how they might respond to hypothesized changes in climate. Critical to these interests is the effect of cold temperature on bacterial activity. Also important is the extent to which marine biological processes in general impact the inorganic carbon cycle. The study area is the Northeast Water (NEW) Polynya, a seasonally-recurrent opening in the permanent ice situated over the northeastern Greenland continental shelf. This work was part of an international, multi-disciplinary research project studying carbon cycling in the coastal Arctic. The first chapter describes a simple model which links a complex marine food web to a simplified ocean and atmosphere. The second chapter investigates the inorganic carbon inventory of the summertime NEW Polynya surface waters to establish the effect of biological processes on the air-sea pCO{sub 2} gradient. The third and fourth chapters use a kinetic approach to examine microbial activities in the NEW Polynya as a function of temperature and dissolved organic substrate concentration, testing the so-called Pomeroy hypothesis that microbial activity is disproportionately reduced at low environmental temperatures owing to increased organic substrate requirements. Together, the suite of data collected on microbial activities, cell size, and grazing pressure suggest how unique survival strategies adopted by an active population of high-latitude bacteria may contribute to, rather than detract from, an efficient biological carbon pump.

  9. Modelling the inorganic ocean carbon cycle under past and future climate change

    International Nuclear Information System (INIS)

    Ewan, T.L.

    2004-01-01

    This study used a coupled ocean-atmosphere-sea ice model with an inorganic carbon component to examine the inorganic ocean carbon cycle with particular reference to how climate feedback influences future uptake. In the last 150 years, the increase in atmosphere carbon dioxide (CO 2 ) concentrations have been higher than any time during the Earth's history. Although the oceans are the largest sink for carbon dioxide, it is not know how the ocean carbon cycle will respond to increasing anthropogenic carbon dioxide concentrations in the future. Climate feedbacks could potentially reduce further uptake of carbon by the ocean. In addition to examining past climate transitions, including both abrupt and glacial-interglacial climate transitions, this study also examined the sensitivity of the inorganic carbon cycle to increased atmospheric carbon dioxide. Atmospheric carbon dioxide levels were also projected under a range of global warming scenarios. Most simulations identified a transient weakening of the North Atlantic and increased sea surface temperatures (SST). These positive feedbacks act on the carbon system to reduce uptake. However, the ocean has the capacity to take up 65 to 75 per cent of the anthropogenic carbon dioxide increases. An analysis of climate feedback on future carbon uptake shows that oceans store 7 per cent more carbon when there are no climate feedbacks acting on the system. Sensitivity experiments using the Gent McWilliams parameterization for mixing associated with mesoscale eddies show a further 6 per cent increase in oceanic uptake. Inclusion of sea ice dynamics resulted in a 2 per cent difference in uptake. This study also examined changes in atmospheric carbon dioxide concentration that occur during abrupt climate change events. Changes in ocean circulation and carbon solubility cause significant increases in atmospheric carbon dioxide concentrations when melt water episodes are simulated in both hemispheres. The response of the carbon

  10. Southern hemisphere ocean CO2 uptake: reconciling atmospheric and oceanic estimates

    International Nuclear Information System (INIS)

    Roy, T.; Matear, R.; Rayner, P.; Francey, R.

    2003-01-01

    Using an atmospheric inversion model we investigate the southern hemisphere ocean CO 2 uptake. From sensitivity studies that varied both the initial ocean flux distribution and the atmospheric data used in the inversion, our inversion predicted a total (ocean and land) uptake of 1.65-1.90 Gt C/yr. We assess the consistency between the mean southern hemisphere ocean uptake predicted by an atmospheric inversion model for the 1991-1997 period and the T99 ocean flux estimate based on observed pCO 2 in Takahashi et al. (2002; Deep-Sea Res II, 49, 1601-1622). The inversion can not match the large 1.8 Gt C/yr southern extratropical (20-90 deg S) uptake of the T99 ocean flux estimate without producing either unreasonable land fluxes in the southern mid-latitudes or by increasing the mismatches between observed and simulated atmospheric CO 2 data. The southern extratropical uptake is redistributed between the mid and high latitudes. Our results suggest that the T99 estimate of the Southern Ocean uptake south of 50 deg S is too large, and that the discrepancy reflects the inadequate representation of wintertime conditions in the T99 estimate

  11. The ocean carbon sink - impacts, vulnerabilities and challenges

    Science.gov (United States)

    Heinze, C.; Meyer, S.; Goris, N.; Anderson, L.; Steinfeldt, R.; Chang, N.; Le Quéré, C.; Bakker, D. C. E.

    2015-06-01

    Carbon dioxide (CO2) is, next to water vapour, considered to be the most important natural greenhouse gas on Earth. Rapidly rising atmospheric CO2 concentrations caused by human actions such as fossil fuel burning, land-use change or cement production over the past 250 years have given cause for concern that changes in Earth's climate system may progress at a much faster pace and larger extent than during the past 20 000 years. Investigating global carbon cycle pathways and finding suitable adaptation and mitigation strategies has, therefore, become of major concern in many research fields. The oceans have a key role in regulating atmospheric CO2 concentrations and currently take up about 25% of annual anthropogenic carbon emissions to the atmosphere. Questions that yet need to be answered are what the carbon uptake kinetics of the oceans will be in the future and how the increase in oceanic carbon inventory will affect its ecosystems and their services. This requires comprehensive investigations, including high-quality ocean carbon measurements on different spatial and temporal scales, the management of data in sophisticated databases, the application of Earth system models to provide future projections for given emission scenarios as well as a global synthesis and outreach to policy makers. In this paper, the current understanding of the ocean as an important carbon sink is reviewed with respect to these topics. Emphasis is placed on the complex interplay of different physical, chemical and biological processes that yield both positive and negative air-sea flux values for natural and anthropogenic CO2 as well as on increased CO2 (uptake) as the regulating force of the radiative warming of the atmosphere and the gradual acidification of the oceans. Major future ocean carbon challenges in the fields of ocean observations, modelling and process research as well as the relevance of other biogeochemical cycles and greenhouse gases are discussed.

  12. Substantial global carbon uptake by cement carbonation

    OpenAIRE

    Xi, Fengming; Davis, Steven J.; Ciais, Philippe; Crawford-Brown, Douglas; Guan, Dabo; Pade, Claus; Shi, Tiemao; Syddall, Mark; Lv, Jie; Ji, Lanzhu; Bing, Longfei; Wang, Jiaoyue; Wei, Wei; Yang, Keun-Hyeok; Lagerblad, Björn

    2016-01-01

    Calcination of carbonate rocks during the manufacture of cement produced 5% of global CO2 emissions from all industrial process and fossil-fuel combustion in 20131, 2. Considerable attention has been paid to quantifying these industrial process emissions from cement production2, 3, but the natural reversal of the process—carbonation—has received little attention in carbon cycle studies. Here, we use new and existing data on cement materials during cement service life, demolition, and secondar...

  13. Bacteria in the greenhouse: Modeling the role of oceanic plankton in the global carbon cycle

    International Nuclear Information System (INIS)

    Ducklow, H.W.; Fasham, M.J.R.

    1992-01-01

    To plan effectively to deal with the greenhouse effect, a fundamental understanding is needed of the biogeochemical and physical machinery that cycles carbon in the global system; in addition, models are needed of the carbon cycle to project the effects of increasing carbon dioxide. In this chapter, a description is given of efforts to simulate the cycling of carbon and nitrogen in the upper ocean, concentrating on the model's treatment of marine phytoplankton, and what it reveals of their role in the biogeochemical cycling of carbon between the ocean and atmosphere. The focus is on the upper ocean because oceanic uptake appears to regulate the level of carbon dioxide in the atmosphere

  14. Ocean acidification and calcium carbonate saturation states in the coastal zone of the West Antarctic Peninsula

    NARCIS (Netherlands)

    Jones, E.M.; Fenton, M.; Meredith, M.P.; Clargo, N.M.; Ossebaar, S.; Ducklow, H.W.; Venables, H.J.; De Baar, H.J.W.

    2017-01-01

    The polar oceans are particularly vulnerable to ocean acidification; the lowering of seawater pH and carbonate mineral saturation states due to uptake of atmospheric carbon dioxide (CO2). High spatial variability in surface water pH and saturation states (Ω) for two biologically-important calcium

  15. Ocean acidification and calcium carbonate saturation states in the coastal zone of the West Antarctic Peninsula

    NARCIS (Netherlands)

    Jones, Elizabeth M.; Fenton, Mairi; Meredith, Michael P.; Clargo, Nicola M.; Ossebaar, Sharyn; Ducklow, Hugh W.; Venables, Hugh J.; de Baar, Henricus

    The polar oceans are particularly vulnerable to ocean acidification; the lowering of seawater pH and carbonate mineral saturation states due to uptake of atmospheric carbon dioxide (CO2). High spatial variability in surface water pH and saturation states (Omega) for two biologically-important

  16. Carbonation and CO2 uptake of concrete

    International Nuclear Information System (INIS)

    Yang, Keun-Hyeok; Seo, Eun-A; Tae, Sung-Ho

    2014-01-01

    This study developed a reliable procedure to assess the carbon dioxide (CO 2 ) uptake of concrete by carbonation during the service life of a structure and by the recycling of concrete after demolition. To generalize the amount of absorbable CO 2 per unit volume of concrete, the molar concentration of carbonatable constituents in hardened cement paste was simplified as a function of the unit content of cement, and the degree of hydration of the cement paste was formulated as a function of the water-to-cement ratio. The contribution of the relative humidity, type of finishing material for the concrete surface, and the substitution level of supplementary cementitious materials to the CO 2 diffusion coefficient in concrete was reflected using various correction factors. The following parameters varying with the recycling scenario were also considered: the carbonatable surface area of concrete crusher-runs and underground phenomena of the decreased CO 2 diffusion coefficient and increased CO 2 concentration. Based on the developed procedure, a case study was conducted for an apartment building with a principal wall system and an office building with a Rahmen system, with the aim of examining the CO 2 uptake of each structural element under different exposure environments during the service life and recycling of the building. As input data necessary for the case study, data collected from actual surveys conducted in 2012 in South Korea were used, which included data on the surrounding environments, lifecycle inventory database, life expectancy of structures, and recycling activity scenario. Ultimately, the CO 2 uptake of concrete during a 100-year lifecycle (life expectancy of 40 years and recycling span of 60 years) was estimated to be 15.5%–17% of the CO 2 emissions from concrete production, which roughly corresponds to 18%–21% of the CO 2 emissions from the production of ordinary Portland cement. - Highlights: • CO 2 uptake assessment approach owing to the

  17. Toward explaining the Holocene carbon dioxide and carbon isotope records: Results from transient ocean carbon cycle-climate simulations

    Science.gov (United States)

    Menviel, L.; Joos, F.

    2012-03-01

    The Bern3D model was applied to quantify the mechanisms of carbon cycle changes during the Holocene (last 11,000 years). We rely on scenarios from the literature to prescribe the evolution of shallow water carbonate deposition and of land carbon inventory changes over the glacial termination (18,000 to 11,000 years ago) and the Holocene and modify these scenarios within uncertainties. Model results are consistent with Holocene records of atmospheric CO2 and δ13C as well as the spatiotemporal evolution of δ13C and carbonate ion concentration in the deep sea. Deposition of shallow water carbonate, carbonate compensation of land uptake during the glacial termination, land carbon uptake and release during the Holocene, and the response of the ocean-sediment system to marine changes during the termination contribute roughly equally to the reconstructed late Holocene pCO2 rise of 20 ppmv. The 5 ppmv early Holocene pCO2 decrease reflects terrestrial uptake largely compensated by carbonate deposition and ocean sediment responses. Additional small contributions arise from Holocene changes in sea surface temperature, ocean circulation, and export productivity. The Holocene pCO2 variations result from the subtle balance of forcings and processes acting on different timescales and partly in opposite direction as well as from memory effects associated with changes occurring during the termination. Different interglacial periods with different forcing histories are thus expected to yield different pCO2 evolutions as documented by ice cores.

  18. Assessing ocean alkalinity for carbon sequestration

    Science.gov (United States)

    Renforth, Phil; Henderson, Gideon

    2017-09-01

    Over the coming century humanity may need to find reservoirs to store several trillions of tons of carbon dioxide (CO2) emitted from fossil fuel combustion, which would otherwise cause dangerous climate change if it were left in the atmosphere. Carbon storage in the ocean as bicarbonate ions (by increasing ocean alkalinity) has received very little attention. Yet recent work suggests sufficient capacity to sequester copious quantities of CO2. It may be possible to sequester hundreds of billions to trillions of tons of C without surpassing postindustrial average carbonate saturation states in the surface ocean. When globally distributed, the impact of elevated alkalinity is potentially small and may help ameliorate the effects of ocean acidification. However, the local impact around addition sites may be more acute but is specific to the mineral and technology. The alkalinity of the ocean increases naturally because of rock weathering in which >1.5 mol of carbon are removed from the atmosphere for every mole of magnesium or calcium dissolved from silicate minerals (e.g., wollastonite, olivine, and anorthite) and 0.5 mol for carbonate minerals (e.g., calcite and dolomite). These processes are responsible for naturally sequestering 0.5 billion tons of CO2 per year. Alkalinity is reduced in the ocean through carbonate mineral precipitation, which is almost exclusively formed from biological activity. Most of the previous work on the biological response to changes in carbonate chemistry have focused on acidifying conditions. More research is required to understand carbonate precipitation at elevated alkalinity to constrain the longevity of carbon storage. A range of technologies have been proposed to increase ocean alkalinity (accelerated weathering of limestone, enhanced weathering, electrochemical promoted weathering, and ocean liming), the cost of which may be comparable to alternative carbon sequestration proposals (e.g., $20-100 tCO2-1). There are still many

  19. A simple model of the effect of ocean ventilation on ocean heat uptake

    Science.gov (United States)

    Nadiga, Balu; Urban, Nathan

    2017-11-01

    Transport of water from the surface mixed layer into the ocean interior is achieved, in large part, by the process of ventilation-a process associated with outcropping isopycnals. Starting from such a configuration of outcropping isopycnals, we derive a simple model of the effect of ventilation on ocean uptake of anomalous radiative forcing. This model can be seen as an improvement of the popular anomaly-diffusing class of energy balance models (AD-EBM) that are routinely employed to analyze and emulate the warming response of both observed and simulated Earth system. We demonstrate that neither multi-layer, nor continuous-diffusion AD-EBM variants can properly represent both surface-warming and the vertical distribution of ocean heat uptake. The new model overcomes this deficiency. The simplicity of the models notwithstanding, the analysis presented and the necessity of the modification is indicative of the role played by processes related to the down-welling branch of global ocean circulation in shaping the vertical distribution of ocean heat uptake.

  20. A simple model of the effect of ocean ventilation on ocean heat uptake

    Energy Technology Data Exchange (ETDEWEB)

    Nadiga, Balasubramanya T. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Urban, Nathan Mark [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2018-01-27

    Presentation includes slides on Earth System Models vs. Simple Climate Models; A Popular SCM: Energy Balance Model of Anomalies; On calibrating against one ESM experiment, the SCM correctly captures that ESM's surface warming response with other forcings; Multi-Model Analysis: Multiple ESMs, Single SCM; Posterior Distributions of ECS; However In Excess of 90% of TOA Energy Imbalance is Sequestered in the World Oceans; Heat Storage in the Two Layer Model; Heat Storage in the Two Layer Model; Including TOA Rad. Imbalance and Ocean Heat in Calibration Improves Repr., but Significant Errors Persist; Improved Vertical Resolution Does Not Fix Problem; A Series of Expts. Confirms That Anomaly-Diffusing Models Cannot Properly Represent Ocean Heat Uptake; Physics of the Thermocline; Outcropping Isopycnals and Horizontally-Averaged Layers; Local interactions between outcropping isopycnals leads to non-local interactions between horizontally-averaged layers; Both Surface Warming and Ocean Heat are Well Represented With Just 4 Layers; A Series of Expts. Confirms That When Non-Local Interactions are Allowed, the SCMs Can Represent Both Surface Warming and Ocean Heat Uptake; and Summary and Conclusions.

  1. Characterizing post-industrial changes in the ocean carbon cycle in an Earth system model

    Energy Technology Data Exchange (ETDEWEB)

    Matsumoto, Katsumi; Tokos, Kathy S.; Chikamoto, Megumi O. (Geology and Geophysics, Univ. of Minnesota, MN (United States)), e-mail: katsumi@umn.edu; Ridgwell, Andy (School of Geographical Sciences, Univ. of Bristol, Bristol (United Kingdom))

    2010-10-22

    Understanding the oceanic uptake of carbon from the atmosphere is essential for better constraining the global budget, as well as for predicting the air-borne fraction of CO{sub 2} emissions and thus degree of climate change. Gaining this understanding is difficult, because the 'natural' carbon cycle, the part of the global carbon cycle unaltered by CO{sub 2} emissions, also responds to climate change and ocean acidification. Using a global climate model of intermediate complexity, we assess the evolution of the natural carbon cycle over the next few centuries. We find that physical mechanisms, particularly Atlantic meridional overturning circulation and gas solubility, alter the natural carbon cycle the most and lead to a significant reduction in the overall oceanic carbon uptake. Important biological mechanisms include reduced organic carbon export production due to reduced nutrient supply, increased organic carbon production due to higher temperatures and reduced CaCO{sub 3} production due to increased ocean acidification. A large ensemble of model experiments indicates that the most important source of uncertainty in ocean uptake projections in the near term future are the upper ocean vertical diffusivity and gas exchange coefficient. By year 2300, the model's climate sensitivity replaces these two and becomes the dominant factor as global warming continues

  2. Coral Carbonic Anhydrases: Regulation by Ocean Acidification.

    Science.gov (United States)

    Zoccola, Didier; Innocenti, Alessio; Bertucci, Anthony; Tambutté, Eric; Supuran, Claudiu T; Tambutté, Sylvie

    2016-06-03

    Global change is a major threat to the oceans, as it implies temperature increase and acidification. Ocean acidification (OA) involving decreasing pH and changes in seawater carbonate chemistry challenges the capacity of corals to form their skeletons. Despite the large number of studies that have investigated how rates of calcification respond to ocean acidification scenarios, comparatively few studies tackle how ocean acidification impacts the physiological mechanisms that drive calcification itself. The aim of our paper was to determine how the carbonic anhydrases, which play a major role in calcification, are potentially regulated by ocean acidification. For this we measured the effect of pH on enzyme activity of two carbonic anhydrase isoforms that have been previously characterized in the scleractinian coral Stylophora pistillata. In addition we looked at gene expression of these enzymes in vivo. For both isoforms, our results show (1) a change in gene expression under OA (2) an effect of OA and temperature on carbonic anhydrase activity. We suggest that temperature increase could counterbalance the effect of OA on enzyme activity. Finally we point out that caution must, thus, be taken when interpreting transcriptomic data on carbonic anhydrases in ocean acidification and temperature stress experiments, as the effect of these stressors on the physiological function of CA will depend both on gene expression and enzyme activity.

  3. Coral Carbonic Anhydrases: Regulation by Ocean Acidification

    Directory of Open Access Journals (Sweden)

    Didier Zoccola

    2016-06-01

    Full Text Available Global change is a major threat to the oceans, as it implies temperature increase and acidification. Ocean acidification (OA involving decreasing pH and changes in seawater carbonate chemistry challenges the capacity of corals to form their skeletons. Despite the large number of studies that have investigated how rates of calcification respond to ocean acidification scenarios, comparatively few studies tackle how ocean acidification impacts the physiological mechanisms that drive calcification itself. The aim of our paper was to determine how the carbonic anhydrases, which play a major role in calcification, are potentially regulated by ocean acidification. For this we measured the effect of pH on enzyme activity of two carbonic anhydrase isoforms that have been previously characterized in the scleractinian coral Stylophora pistillata. In addition we looked at gene expression of these enzymes in vivo. For both isoforms, our results show (1 a change in gene expression under OA (2 an effect of OA and temperature on carbonic anhydrase activity. We suggest that temperature increase could counterbalance the effect of OA on enzyme activity. Finally we point out that caution must, thus, be taken when interpreting transcriptomic data on carbonic anhydrases in ocean acidification and temperature stress experiments, as the effect of these stressors on the physiological function of CA will depend both on gene expression and enzyme activity.

  4. Oceanic uptake of CO2 re-estimated through δ13C in WOCE samples

    International Nuclear Information System (INIS)

    Lerperger, Michael; McNichol, A.P.; Peden, J.; Gagnon, A.R.; Elder, K.L.; Kutschera, W.; Rom, W.; Steier, P.

    2000-01-01

    In addition to 14 C, a large set of δ 13 C data was produced at NOSAMS as part of the World ocean circulation experiment (WOCE). In this paper, a subset of 973 δ 13 C results from 63 stations in the Pacific Ocean was compared to a total number of 219 corresponding results from 12 stations sampled during oceanographic programs in the early 1970s. The data were analyzed in light of recent work to estimate the uptake of CO 2 derived from fossil fuel and biomass burning in the oceans by quantifying the δ 13 C Suess effect in the oceans. In principle, the δ 13 C value of dissolved inorganic carbon (DIC) allows a quantitative estimate of how much of the anthropogenic CO 2 released into the atmosphere is taken up by the oceans, because the δ 13 C of CO 2 derived from organic matter (∼2.7 percent) is significantly different from that of the atmosphere (∼0.8 percent). Our new analysis indicates an apparent discrepancy between the old and the new data sets, possibly caused by a constant offset in δ 13 C values in a subset of the data. A similar offset was reported in an earlier work by Paul Quay et al. for one station that was not included in their final analysis. We present an estimate for this assumed offset based on data from water depths below which little or no change in δ 13 C over time would be expected. Such a correction leads to a significantly reduced estimate of the CO 2 uptake, possibly as low as one half of the amount of 2.1 GtC yr -1 (gigatons carbon per year) estimated previously. The present conclusion is based on a comparison with a relatively small data set from the 70s in the Pacific Ocean. The larger data set collected during the GEOSECS program was not used because of problems reported with the data. This work suggests there may also be problems in comparing non-GEOSECS data from the 1970s to the current data. The calculation of significantly lower uptake estimates based on an offset-related problem appears valid, but the exact figures are

  5. Gradients in microbial methanol uptake: productive coastal upwelling waters to oligotrophic gyres in the Atlantic Ocean

    Science.gov (United States)

    Dixon, Joanna L; Sargeant, Stephanie; Nightingale, Philip D; Colin Murrell, J

    2013-01-01

    Methanol biogeochemistry and its importance as a carbon source in seawater is relatively unexplored. We report the first microbial methanol carbon assimilation rates (k) in productive coastal upwelling waters of up to 0.117±0.002 d−1 (∼10 nmol l−1 d−1). On average, coastal upwelling waters were 11 times greater than open ocean northern temperate (NT) waters, eight times greater than gyre waters and four times greater than equatorial upwelling (EU) waters; suggesting that all upwelling waters upon reaching the surface (⩽20 m), contain a microbial population that uses a relatively high amount of carbon (0.3–10 nmol l−1 d−1), derived from methanol, to support their growth. In open ocean Atlantic regions, microbial uptake of methanol into biomass was significantly lower, ranging between 0.04–0.68 nmol l−1 d−1. Microbes in the Mauritanian coastal upwelling used up to 57% of the total methanol for assimilation of the carbon into cells, compared with an average of 12% in the EU, and 1% in NT and gyre waters. Several methylotrophic bacterial species were identified from open ocean Atlantic waters using PCR amplification of mxaF encoding methanol dehydrogenase, the key enzyme in bacterial methanol oxidation. These included Methylophaga sp., Burkholderiales sp., Methylococcaceae sp., Ancylobacter aquaticus, Paracoccus denitrificans, Methylophilus methylotrophus, Methylobacterium oryzae, Hyphomicrobium sp. and Methylosulfonomonas methylovora. Statistically significant correlations for upwelling waters between methanol uptake into cells and both chlorophyll a concentrations and methanol oxidation rates suggest that remotely sensed chlorophyll a images, in these productive areas, could be used to derive total methanol biological loss rates, a useful tool for atmospheric and marine climatically active gas modellers, and air–sea exchange scientists. PMID:23178665

  6. Carbon-climate feedbacks accelerate ocean acidification

    Science.gov (United States)

    Matear, Richard J.; Lenton, Andrew

    2018-03-01

    Carbon-climate feedbacks have the potential to significantly impact the future climate by altering atmospheric CO2 concentrations (Zaehle et al. 2010). By modifying the future atmospheric CO2 concentrations, the carbon-climate feedbacks will also influence the future ocean acidification trajectory. Here, we use the CO2 emissions scenarios from four representative concentration pathways (RCPs) with an Earth system model to project the future trajectories of ocean acidification with the inclusion of carbon-climate feedbacks. We show that simulated carbon-climate feedbacks can significantly impact the onset of undersaturated aragonite conditions in the Southern and Arctic oceans, the suitable habitat for tropical coral and the deepwater saturation states. Under the high-emissions scenarios (RCP8.5 and RCP6), the carbon-climate feedbacks advance the onset of surface water under saturation and the decline in suitable coral reef habitat by a decade or more. The impacts of the carbon-climate feedbacks are most significant for the medium- (RCP4.5) and low-emissions (RCP2.6) scenarios. For the RCP4.5 scenario, by 2100 the carbon-climate feedbacks nearly double the area of surface water undersaturated with respect to aragonite and reduce by 50 % the surface water suitable for coral reefs. For the RCP2.6 scenario, by 2100 the carbon-climate feedbacks reduce the area suitable for coral reefs by 40 % and increase the area of undersaturated surface water by 20 %. The sensitivity of ocean acidification to the carbon-climate feedbacks in the low to medium emission scenarios is important because recent CO2 emission reduction commitments are trying to transition emissions to such a scenario. Our study highlights the need to better characterise the carbon-climate feedbacks and ensure we do not underestimate the projected ocean acidification.

  7. Southern Ocean carbon-wind stress feedback

    Science.gov (United States)

    Bronselaer, Ben; Zanna, Laure; Munday, David R.; Lowe, Jason

    2018-02-01

    The Southern Ocean is the largest sink of anthropogenic carbon in the present-day climate. Here, Southern Ocean pCO2 and its dependence on wind forcing are investigated using an equilibrium mixed layer carbon budget. This budget is used to derive an expression for Southern Ocean pCO2 sensitivity to wind stress. Southern Ocean pCO2 is found to vary as the square root of area-mean wind stress, arising from the dominance of vertical mixing over other processes such as lateral Ekman transport. The expression for pCO2 is validated using idealised coarse-resolution ocean numerical experiments. Additionally, we show that increased (decreased) stratification through surface warming reduces (increases) the sensitivity of the Southern Ocean pCO2 to wind stress. The scaling is then used to estimate the wind-stress induced changes of atmospheric pCO_2 in CMIP5 models using only a handful of parameters. The scaling is further used to model the anthropogenic carbon sink, showing a long-term reversal of the Southern Ocean sink for large wind stress strength.

  8. The Arctic Ocean marine carbon cycle: evaluation of air-sea CO2 exchanges, ocean acidification impacts and potential feedbacks

    Directory of Open Access Journals (Sweden)

    N. R. Bates

    2009-11-01

    Full Text Available At present, although seasonal sea-ice cover mitigates atmosphere-ocean gas exchange, the Arctic Ocean takes up carbon dioxide (CO2 on the order of −66 to −199 Tg C year−1 (1012 g C, contributing 5–14% to the global balance of CO2 sinks and sources. Because of this, the Arctic Ocean has an important influence on the global carbon cycle, with the marine carbon cycle and atmosphere-ocean CO2 exchanges sensitive to Arctic Ocean and global climate change feedbacks. In the near-term, further sea-ice loss and increases in phytoplankton growth rates are expected to increase the uptake of CO2 by Arctic Ocean surface waters, although mitigated somewhat by surface warming in the Arctic. Thus, the capacity of the Arctic Ocean to uptake CO2 is expected to alter in response to environmental changes driven largely by climate. These changes are likely to continue to modify the physics, biogeochemistry, and ecology of the Arctic Ocean in ways that are not yet fully understood. In surface waters, sea-ice melt, river runoff, cooling and uptake of CO2 through air-sea gas exchange combine to decrease the calcium carbonate (CaCO3 mineral saturation states (Ω of seawater while seasonal phytoplankton primary production (PP mitigates this effect. Biological amplification of ocean acidification effects in subsurface waters, due to the remineralization of organic matter, is likely to reduce the ability of many species to produce CaCO3 shells or tests with profound implications for Arctic marine ecosystems

  9. Ultraviolet-B radiation effects on inorganic nitrogen uptake by natural assemblages of oceanic plankton

    International Nuclear Information System (INIS)

    Behrenfeld, M.J.; Lean, D.R.S.; Lee, H. II

    1995-01-01

    Ultraviolet-B radiation (UVBR: 290-320 nm) inhibited ammonium uptake (ρ NH4 ) and nitrate uptake (ρ NO3 ) in natural plankton assemblages collected during a transect from 37 degrees N to 55 degrees N in the Pacific Ocean. Comparison of responses in ρ NH4 to ambient solar- and lamp-enhanced UVBR spectra allowed calculation of an action spectrum for ρ NH4 inhibition. The slope of the action spectrum for ρ NH4 is half as steep as action spectra for UVBR inhibition of photosynthetic carbon uptake. Consequently, UVBR-induced photoinhibition of ρ NH4 extends to greater depths than inhibition of carbon fixation due to the greater relative effect of longer UVBR wavelengths. Inhibition of ρ NH4 was dependent upon UVBR dose when doses were weighted by the ρ NH4 action spectrum. Dependence of UVBR inhibition of ρ NH4 on dose rate was not apparent. We found that near-surface ρ NH4 and ρ NO3 can be overestimated in excess of 50% when measured using standard incubation vessels made of UVBR-absorbing materials such as polycarbonate. 68 refs., 9 figs., 1 tab

  10. Radiocarbon evidence for a smaller oceanic carbon dioxide sink than previously believed

    Science.gov (United States)

    Hesshaimer, Vago; Heimann, Martin; Levin, Ingeborg

    1994-07-01

    RADIOCARBON produced naturally in the upper atmosphere or arti-ficially during nuclear weapons testing is the main tracer used to validate models of oceanic carbon cycling, in particular the exchange of carbon dioxide with the atmosphere1-3 and the mixing parameters within the ocean itself4-7. Here we test the overall consistency of exchange fluxes between all relevant compartments in a simple model of the global carbon cycle, using measurements of the long-term tropospheric CO2 concentration8 and radiocarbon composition9-12, the bomb 14C inventory in the stratosphere13,14 and a compilation of bomb detonation dates and strengths15. We find that to balance the budget, we must invoke an extra source to account for 25% of the generally accepted uptake of bomb 14C by the oceans3. The strength of this source decreases from 1970 onwards, with a characteristic timescale similar to that of the ocean uptake. Significant radiocarbon transport from the remote high stratosphere and significantly reduced uptake of bomb 14C by the biosphere can both be ruled out by observational constraints. We therefore conclude that the global oceanic bomb 14C inventory should be revised downwards. A smaller oceanic bomb 14C inventory also implies a smaller oceanic radiocarbon penetration depth16, which in turn implies that the oceans take up 25% less anthropogenic CO2 than had previously been believed.

  11. Carbonate compensation depth: relation to carbonate solubility in ocean waters.

    Science.gov (United States)

    Ben-Yaakov, S; Ruth, E; Kaplan, I R

    1974-05-31

    In situ calcium carbonate saturometry measurements suggest that the intermediate water masses of the central Pacific Ocean are close to saturation with resppect to both calcite and local carbonate sediment. The carbonate compensation depth, located at about 3700 meters in this area, appears to represent a depth above which waters are essentially saturated with respect to calcite and below which waters deviate toward undersaturation with respect to calcite.

  12. An isopycnic ocean carbon cycle model

    Directory of Open Access Journals (Sweden)

    K. M. Assmann

    2010-02-01

    Full Text Available The carbon cycle is a major forcing component in the global climate system. Modelling studies, aiming to explain recent and past climatic changes and to project future ones, increasingly include the interaction between the physical and biogeochemical systems. Their ocean components are generally z-coordinate models that are conceptually easy to use but that employ a vertical coordinate that is alien to the real ocean structure. Here, we present first results from a newly-developed isopycnic carbon cycle model and demonstrate the viability of using an isopycnic physical component for this purpose. As expected, the model represents well the interior ocean transport of biogeochemical tracers and produces realistic tracer distributions. Difficulties in employing a purely isopycnic coordinate lie mainly in the treatment of the surface boundary layer which is often represented by a bulk mixed layer. The most significant adjustments of the ocean biogeochemistry model HAMOCC, for use with an isopycnic coordinate, were in the representation of upper ocean biological production. We present a series of sensitivity studies exploring the effect of changes in biogeochemical and physical processes on export production and nutrient distribution. Apart from giving us pointers for further model development, they highlight the importance of preformed nutrient distributions in the Southern Ocean for global nutrient distributions. The sensitivity studies show that iron limitation for biological particle production, the treatment of light penetration for biological production, and the role of diapycnal mixing result in significant changes of nutrient distributions and liniting factors of biological production.

  13. Linkages between ocean circulation, heat uptake and transient warming: a sensitivity study

    Science.gov (United States)

    Pfister, Patrik; Stocker, Thomas

    2016-04-01

    Transient global warming due to greenhouse gas radiative forcing is substantially reduced by ocean heat uptake (OHU). However, the fraction of equilibrium warming that is realized in transient climate model simulations differs strongly between models (Frölicher and Paynter 2015). It has been shown that this difference is not only related to the magnitude of OHU, but also to the radiative response the OHU causes, measured by the OHU efficacy (Winton et al., 2010). This efficacy is strongly influenced by the spatial pattern of the OHU and its changes (Rose et al. 2014, Winton et al. 2013), predominantly caused by changes in the Atlantic meridional overturning circulation (AMOC). Even in absence of external greenhouse gas forcing, an AMOC weakening causes a radiative imbalance at the top of the atmosphere (Peltier and Vettoretti, 2014), inducing in a net warming of the Earth System. We investigate linkages between those findings by performing both freshwater and greenhouse gas experiments in an Earth System Model of Intermediate Complexity. To assess the sensitivity of the results to ocean and atmospheric transport as well as climate sensitivity, we use an ensemble of model versions, systematically varying key parameters. We analyze circulation changes and radiative adjustments in conjunction with traditional warming metrics such as the transient climate response and the equilibrium climate sensitivity. This aims to improve the understanding of the influence of ocean circulation and OHU on transient climate change, and of the relevance of different metrics for describing this influence. References: Frölicher, T. L. and D.J. Paynter (2015), Extending the relationship between global warming and cumulative carbon emissions to multi-millennial timescales, Environ. Res. Lett., 10, 075022 Peltier, W. R., and G. Vettoretti (2014), Dansgaard-Oeschger oscillations predicted in a comprehensive model of glacial climate: A "kicked" salt oscillator in the Atlantic, Geophys. Res

  14. Sudden increase in atmospheric concentration reveals strong coupling between shoot carbon uptake and root nutrient uptake in young walnut trees

    International Nuclear Information System (INIS)

    Delaire, M.; Sigogne, M.; Beaujard, F.; Frak, E.; Adam, B.; Le Roux, X.

    2005-01-01

    Short-term effects of a sudden increase in carbon dioxide concentration on nutrient uptake by roots during vegetative growth was studied in young walnut trees. Rates of carbon dioxide uptake and water loss by individual trees were determined by a branch bag method from three days before and six days after carbon dioxide concentration was increased. Nutrient uptake rates were measured concurrently by a hydroponic recirculating nutrient solution system. Carbon dioxide uptake rates increased greatly with increasing atmospheric carbon dioxide; nutrient uptake rates were proportional to carbon dioxide uptake rates, except for the phosphorus ion. Daily water loss rates were only slightly affected by elevated carbon dioxide. Overall, it was concluded that in the presence of non-limiting supplies of water and nutrients, root nutrient uptake and shoot carbon assimilation are strongly coupled in the short term in young walnut trees despite the important carbon and nutrient storage capacities od woody species. 45 refs., 7 figs

  15. Eddy correlation measurements of oxygen uptake in deep ocean sediments

    DEFF Research Database (Denmark)

    Berg, P.; Glud, Ronnie Nøhr; Hume, A.

    2010-01-01

    .62 +/- 0.23 (SE, n = 7), 1.65 +/- 0.33 (n = 2), and 1.43 +/- 0.15 (n = 25) mmol m(-2) d(-1). The very good agreement between the eddy correlation flux and the chamber flux serves as a new, important validation of the eddy correlation technique. It demonstrates that the eddy correlation instrumentation......Abstract: We present and compare small sediment-water fluxes of O-2 determined with the eddy correlation technique, with in situ chambers, and from vertical sediment microprofiles at a 1450 m deep-ocean site in Sagami Bay, Japan. The average O-2 uptake for the three approaches, respectively, was 1...... available today is precise and can resolve accurately even very small benthic O-2 fluxes. The correlated fluctuations in vertical velocity and O-2 concentration that give the eddy flux had average values of 0.074 cm s(-1) and 0.049 mu M. The latter represents only 0.08% of the 59 mu M mean O-2 concentration...

  16. Calcium carbonate production response to future ocean warming and acidification

    Directory of Open Access Journals (Sweden)

    A. J. Pinsonneault

    2012-06-01

    Full Text Available Anthropogenic carbon dioxide (CO2 emissions are acidifying the ocean, affecting calcification rates in pelagic organisms, and thereby modifying the oceanic carbon and alkalinity cycles. However, the responses of pelagic calcifying organisms to acidification vary widely between species, contributing uncertainty to predictions of atmospheric CO2 and the resulting climate change. At the same time, ocean warming caused by rising CO2 is expected to drive increased growth rates of all pelagic organisms, including calcifiers. It thus remains unclear whether anthropogenic CO2 emissions will ultimately increase or decrease pelagic calcification rates. Here, we assess the importance of this uncertainty by introducing a dependence of calcium carbonate (CaCO3 production on calcite saturation state (ΩCaCO3 in an intermediate complexity coupled carbon-climate model. In a series of model simulations, we examine the impact of several variants of this dependence on global ocean carbon cycling between 1800 and 3500 under two different CO2 emissions scenarios. Introducing a calcification-saturation state dependence has a significant effect on the vertical and surface horizontal alkalinity gradients, as well as on the removal of alkalinity from the ocean through CaCO3 burial. These changes result in an additional oceanic uptake of carbon when calcification depends on ΩCaCO3 (of up to 270 Pg C, compared to the case where calcification does not depend on acidification. In turn, this response causes a reduction of global surface air temperature of up to 0.4 °C in year 3500. Different versions of the model produced varying results, and narrowing this range of uncertainty will require better understanding of both temperature and acidification effects on pelagic calcifiers. Nevertheless, our results suggest that alkalinity observations can be used

  17. Deciphering ocean carbon in a changing world

    Energy Technology Data Exchange (ETDEWEB)

    Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron; Fatland, Rob; Aluwihare, Lihini I.; Buchan, Alison; Crump, Byron C.; Dorrestein, Pieter C.; Dyhrman, Sonya T.; Hess, Nancy J.; Howe, Bill; Longnecker, Krista; Medeiros, Patricia M.; Niggemann, Jutta; Obernosterer, Ingrid; Repeta, Daniel J.; Waldbauer, Jacob R.

    2016-03-07

    Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because both DOM and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Here we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.

  18. The declining uptake rate of atmospheric CO2 by land and ocean sinks

    International Nuclear Information System (INIS)

    Raupach, M.R.; Gloor, M.; Sarmiento, J.L.; Gasser, T.

    2014-01-01

    Through 1959-2012, an airborne fraction (AF) of 0.44 of total anthropogenic CO 2 emissions remained in the atmosphere, with the rest being taken up by land and ocean CO 2 sinks. Understanding of this uptake is critical because it greatly alleviates the emissions reductions required for climate mitigation, and also reduces the risks and damages that adaptation has to embrace. An observable quantity that reflects sink properties more directly than the AF is the CO 2 sink rate (k S ), the combined land-ocean CO 2 sink flux per unit excess atmospheric CO 2 above pre industrial levels. Here we show from observations that k S declined over 1959-2012 by a factor of about 1/3, implying that CO 2 sinks increased more slowly than excess CO 2 . Using a carbon-climate model, we attribute the decline in k S to four mechanisms: slower-than-exponential CO 2 emissions growth (35% of the trend), volcanic eruptions (25 %), sink responses to climate change (20 %), and nonlinear responses to increasing CO 2 , mainly oceanic (20 %). The first of these mechanisms is associated purely with the trajectory of extrinsic forcing, and the last two with intrinsic, feedback responses of sink processes to changes in climate and atmospheric CO 2 . Our results suggest that the effects of these intrinsic, nonlinear responses are already detectable in the global carbon cycle. Although continuing future decreases in k S will occur under all plausible CO 2 emission scenarios, the rate of decline varies between scenarios in non intuitive ways because extrinsic and intrinsic mechanisms respond in opposite ways to changes in emissions: extrinsic mechanisms cause k S to decline more strongly with increasing mitigation, while intrinsic mechanisms cause k S to decline more strongly under high-emission, low-mitigation scenarios as the carbon-climate system is perturbed further from a near-linear regime. (authors)

  19. Ocean carbon sequestration by fertilization: An integrated bioeochemical assessment

    Energy Technology Data Exchange (ETDEWEB)

    Gruber, N.; Sarmiento, J.L.; Gnandesikan, A.

    2005-05-31

    Under this grant, the authors investigated a range of issues associated with the proposal to fertilize the ocean with nutrients (such as iron) in order to increase the export of organic matter from the ocean's near surface waters and consequently increase the uptake of CO{sub 2} from the atmosphere. There are several critical scientific questions that have the potential to be make-or-break issues for this proposed carbon sequestration mechanism: (1) If iron is added to the ocean, will export of organic carbon from the surface actually occur? Clearly, if no export occurs, then there will be no sequestration. (2) if iron fertilization does lead to export of organic carbon from the surface of the ocean, how much CO{sub 2} will actually be removed from the atmosphere? Even if carbon is removed from the surface of the ocean, this does not guarantee that there will be significant removal of CO{sub 2} from the atmosphere, since the CO{sub 2} may be supplied by a realignment of dissolved inorganic carbon within the ocean. (3) What is the time scale of any sequestration that occurs? If sequestered CO{sub 2} returns to the atmosphere on a relatively short time scale, iron fertilization will not contribute significantly to slowing the growth of atmospheric CO{sub 2}. (4) Can the magnitude of sequestration be verified? If verification is extremely difficult or impossible, this option is likely to be viewed less favorably. (5) What unintended consequences might there be from fertilizing the ocean with iron? If these are severe enough, they will be a significant impact on policy decisions. Most research on carbon sequestration by fertilization has focused on the first of these issues. Although a number of in situ fertilization experiments have successfully demonstrated that the addition of iron leads to a dramatic increase in ocean productivity, the question of whether this results in enhanced export remains an open one. The primary focus of the research was on the

  20. A new look at ocean carbon remineralization for estimating deepwater sequestration

    DEFF Research Database (Denmark)

    Guidi, L.; Legendre, L.; Reygondeau, Gabriel

    2015-01-01

    provinces, where these estimates range between -50 and +100% of the commonly used globally uniform remineralization value. We apply the regionalized values to satellite-derived estimates of upper ocean POC export to calculate regionalized and ocean-wide deep carbon fluxes and sequestration. The resulting....... These results stress that variable remineralization and sequestration depth should be used to model ocean carbon sequestration and feedback on the atmosphere......The "biological carbon pump" causes carbon sequestration in deep waters by downward transfer of organic matter, mostly as particles. This mechanism depends to a great extent on the uptake of CO2 by marine plankton in surface waters and subsequent sinking of particulate organic carbon (POC) through...

  1. DOE Ocean Carbon Sequestration Research Workshop 2005

    Energy Technology Data Exchange (ETDEWEB)

    Sarmiento, Jorge L. [Princeton Univ., NJ (United States); Chavez, Francisco [Monterey Bay Aquarium Research Inst. (MBARI), Moss Landing, CA (United States); Maltrud, Matthew [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Adams, Eric [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Arrigo, Kevin [Stanford Univ., CA (United States). Dept. of Geophysics; Barry, James [Monterey Bay Aquarium Research Inst. (MBARI), Moss Landing, CA (United States); Carmen, Kevin [Louisiana State Univ., Baton Rouge, LA (United States); Bishop, James [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Bleck, Rainer [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Gruber, Niki [Univ. of California, Los Angeles, CA (United States); Erickson, David [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Kennett, James [Univ. of California, Santa Barbara, CA (United States); Tsouris, Costas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Tagliabue, Alessandro [Lab. of Climate and Environmental Sciences (LSCE), Gif-sur-Yvette (France); Paytan, Adina [Stanford Univ., CA (United States); Repeta, Daniel [Woods Hole Oceanographic Inst. (WHOI), Woods Hole, MA (United States); Yager, Patricia L. [Univ. of Georgia, Athens, GA (United States); Marshall, John [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Gnanadesikan, Anand [Geophysical Fluid Dynamics Lab. (GFDL), Princeton, NJ (United States)

    2007-01-11

    The purpose of this proposal was to fund a workshop to bring together the principal investigators of all the projects that were being funded under the DOE ocean carbon sequestration research program. The primary goal of the workshop was to interchange research results, to discuss ongoing research, and to identify future research priorities. In addition, we hoped to encourage the development of synergies and collaborations between the projects and to write an EOS article summarizing the results of the meeting. Appendix A summarizes the plan of the workshop as originally proposed, Appendix B lists all the principal investigators who were able to attend the workshop, Appendix C shows the meeting agenda, and Appendix D lists all the abstracts that were provided prior to the meeting. The primary outcome of the meeting was a decision to write two papers for the reviewed literature on carbon sequestration by iron fertilization, and on carbon sequestration by deep sea injection and to examine the possibility of an overview article in EOS on the topic of ocean carbon sequestration.

  2. Carbonate-sensitive phytotransferrin controls high-affinity iron uptake in diatoms

    Science.gov (United States)

    McQuaid, Jeffrey B.; Kustka, Adam B.; Oborník, Miroslav; Horák, Aleš; McCrow, John P.; Karas, Bogumil J.; Zheng, Hong; Kindeberg, Theodor; Andersson, Andreas J.; Barbeau, Katherine A.; Allen, Andrew E.

    2018-03-01

    In vast areas of the ocean, the scarcity of iron controls the growth and productivity of phytoplankton. Although most dissolved iron in the marine environment is complexed with organic molecules, picomolar amounts of labile inorganic iron species (labile iron) are maintained within the euphotic zone and serve as an important source of iron for eukaryotic phytoplankton and particularly for diatoms. Genome-enabled studies of labile iron utilization by diatoms have previously revealed novel iron-responsive transcripts, including the ferric iron-concentrating protein ISIP2A, but the mechanism behind the acquisition of picomolar labile iron remains unknown. Here we show that ISIP2A is a phytotransferrin that independently and convergently evolved carbonate ion-coordinated ferric iron binding. Deletion of ISIP2A disrupts high-affinity iron uptake in the diatom Phaeodactylum tricornutum, and uptake is restored by complementation with human transferrin. ISIP2A is internalized by endocytosis, and manipulation of the seawater carbonic acid system reveals a second-order dependence on the concentrations of labile iron and carbonate ions. In P. tricornutum, the synergistic interaction of labile iron and carbonate ions occurs at environmentally relevant concentrations, revealing that carbonate availability co-limits iron uptake. Phytotransferrin sequences have a broad taxonomic distribution and are abundant in marine environmental genomic datasets, suggesting that acidification-driven declines in the concentration of seawater carbonate ions will have a negative effect on this globally important eukaryotic iron acquisition mechanism.

  3. Bacterial uptake of photosynthetic carbon from freshwater phytoplankton

    International Nuclear Information System (INIS)

    Coveney, M.F.

    1982-01-01

    Microheterotrophic uptake of algal extracellular products was studied in two eutrophic lakes in southern Sweden. Size fractionation was used in H 14 CO 3 uptake experiments to measure 14 C fixation in total particulate, small particulate and dissolved organic fractions. Carbon fixed in algal photosynthesis was recovered as dissolved and small particulate 14 C, representing excretion and bacterial uptake of algal products. Estimated gross extracellular release was low in these eutrophic systems, 1 to 7% of total 14 C uptake per m 2 lake surface. From 28 to 80 % of 14 C released was recovered in the small particulate fraction after ca. 4h incubation.This percentage was uniform within each depth profile, but varied directly with in situ water temperature. Laboratory time-series incubations indicated steady state for the pool of algal extracellular products on one occasion, while increasing pool size was indicated in the remaining two experiments. Uptake of photosynthetic carbon to small particles in situ was 32 to 95% of estimted heterotrophic bacterial production (as dark 14 CO 2 uptake) on four occasions. While excretion apparently was not an important loss of cabon for phytoplankton, it may have represented an important carbon source for planktonic bacteria. (author)

  4. Uptake mechanism for iodine species to black carbon.

    Science.gov (United States)

    Choung, Sungwook; Um, Wooyong; Kim, Minkyung; Kim, Min-Gyu

    2013-09-17

    Natural organic matter (NOM) plays an important role in determining the fate and transport of iodine species such as iodide (I(-)) and iodate (IO3(-)) in groundwater system. Although NOM exists as diverse forms in environments, prior iodine studies have mainly focused on uptake processes of iodide and iodate to humic materials. This study was conducted to determine the iodide and iodate uptake potential for a particulate NOM (i.e., black carbon [BC]). A laboratory-produced BC and commercial humic acid were used for batch experiments to compare their iodine uptake properties. The BC exhibited >100 times greater uptake capability for iodide than iodate at low pH of ~3, while iodide uptake was negligible for the humic acid. The uptake properties of both solids strongly depend on the initial iodine aqueous concentrations. After uptake reaction of iodide to the BC, X-ray absorption fine structure spectroscopy results indicated that the iodide was converted to electrophilic species, and iodine was covalently bound to carbon atom in polycyclic aromatic hydrocarbons present in the BC. The computed distribution coefficients (i.e., Kd values) suggest that the BC materials retard significantly the transport of iodide at low pH in environmental systems containing even a small amount of BC.

  5. Deciphering ocean carbon in a changing world.

    Science.gov (United States)

    Moran, Mary Ann; Kujawinski, Elizabeth B; Stubbins, Aron; Fatland, Rob; Aluwihare, Lihini I; Buchan, Alison; Crump, Byron C; Dorrestein, Pieter C; Dyhrman, Sonya T; Hess, Nancy J; Howe, Bill; Longnecker, Krista; Medeiros, Patricia M; Niggemann, Jutta; Obernosterer, Ingrid; Repeta, Daniel J; Waldbauer, Jacob R

    2016-03-22

    Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO2 reservoir. A vast number of compounds are present in DOM, and they play important roles in all major element cycles, contribute to the storage of atmospheric CO2 in the ocean, support marine ecosystems, and facilitate interactions between organisms. At the heart of the DOM cycle lie molecular-level relationships between the individual compounds in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have eluded clear definition because of the sheer numerical complexity of both DOM molecules and microorganisms. Emerging tools in analytical chemistry, microbiology, and informatics are breaking down the barriers to a fuller appreciation of these connections. Here we highlight questions being addressed using recent methodological and technological developments in those fields and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.

  6. The Role of Refractory Dissolved Organic Matter in Ocean Carbon Sequestration

    DEFF Research Database (Denmark)

    Jørgensen, Linda

    The ocean assimilates a large amount of atmospheric CO2 and is potentially a buffer for climate change. A fraction of the assimilated CO2 is incorporated into algal biomass and further converted into refractory dissolved organic matter (DOM). Carbon bound in refractory DOM has the potential...... studies the prokaryotic production and degradation of oceanic refractory DOM and discusses the reasons for the persistent nature of this large DOM fraction. The first two papers investigate the microbial carbon pump, i.e. prokaryotic transfor-mation of organic carbon into refractory DOM. The results show...... DOM compounds in the ocean are rare—possibly too rare to sustain viable uptake and assimilation. Hence, the dilute concentration of individual compounds is a possible explanation for the apparent refractory nature of most DOM in the ocean. Understanding the mechanisms that control the quality...

  7. Dynamical and biogeochemical control on the decadal variability of ocean carbon fluxes

    Directory of Open Access Journals (Sweden)

    R. Séférian

    2013-04-01

    Full Text Available Several recent observation-based studies suggest that ocean anthropogenic carbon uptake has slowed down due to the impact of anthropogenic forced climate change. However, it remains unclear whether detected changes over the recent time period can be attributed to anthropogenic climate change or rather to natural climate variability (internal plus naturally forced variability alone. One large uncertainty arises from the lack of knowledge on ocean carbon flux natural variability at the decadal time scales. To gain more insights into decadal time scales, we have examined the internal variability of ocean carbon fluxes in a 1000 yr long preindustrial simulation performed with the Earth System Model IPSL-CM5A-LR. Our analysis shows that ocean carbon fluxes exhibit low-frequency oscillations that emerge from their year-to-year variability in the North Atlantic, the North Pacific, and the Southern Ocean. In our model, a 20 yr mode of variability in the North Atlantic air-sea carbon flux is driven by sea surface temperature variability and accounts for ~40% of the interannual regional variance. The North Pacific and the Southern Ocean carbon fluxes are also characterised by decadal to multi-decadal modes of variability (10 to 50 yr that account for 20–40% of the interannual regional variance. These modes are driven by the vertical supply of dissolved inorganic carbon through the variability of Ekman-induced upwelling and deep-mixing events. Differences in drivers of regional modes of variability stem from the coupling between ocean dynamics variability and the ocean carbon distribution, which is set by large-scale secular ocean circulation.

  8. Carbon dioxide and nitrous oxide in the North Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    DileepKumar, M.; Naqvi, S.W.A; Jayakumar, D.A; George, M.D.; Narvekar, P.V.; DeSousa, S

    The understanding of biogeochemical cycling of carbon dioxide and nitrous oxide in the oceans is essential for predicting the fate of anthropogenically emitted components. The North Indian Ocean, with its diverse regimes, provides us with a natural...

  9. Spring hydrology determines summer net carbon uptake in northern ecosystems

    International Nuclear Information System (INIS)

    Yi, Yonghong; Kimball, John S; Reichle, Rolf H

    2014-01-01

    Increased photosynthetic activity and enhanced seasonal CO 2 exchange of northern ecosystems have been observed from a variety of sources including satellite vegetation indices (such as the normalized difference vegetation index; NDVI) and atmospheric CO 2 measurements. Most of these changes have been attributed to strong warming trends in the northern high latitudes (⩾50° N). Here we analyze the interannual variation of summer net carbon uptake derived from atmospheric CO 2 measurements and satellite NDVI in relation to surface meteorology from regional observational records. We find that increases in spring precipitation and snow pack promote summer net carbon uptake of northern ecosystems independent of air temperature effects. However, satellite NDVI measurements still show an overall benefit of summer photosynthetic activity from regional warming and limited impact of spring precipitation. This discrepancy is attributed to a similar response of photosynthesis and respiration to warming and thus reduced sensitivity of net ecosystem carbon uptake to temperature. Further analysis of boreal tower eddy covariance CO 2 flux measurements indicates that summer net carbon uptake is positively correlated with early growing-season surface soil moisture, which is also strongly affected by spring precipitation and snow pack based on analysis of satellite soil moisture retrievals. This is attributed to strong regulation of spring hydrology on soil respiration in relatively wet boreal and arctic ecosystems. These results document the important role of spring hydrology in determining summer net carbon uptake and contrast with prevailing assumptions of dominant cold temperature limitations to high-latitude ecosystems. Our results indicate potentially stronger coupling of boreal/arctic water and carbon cycles with continued regional warming trends. (letters)

  10. Spring Hydrology Determines Summer Net Carbon Uptake in Northern Ecosystems

    Science.gov (United States)

    Yi, Yonghong; Kimball, John; Reichle, Rolf H.

    2014-01-01

    Increased photosynthetic activity and enhanced seasonal CO2 exchange of northern ecosystems have been observed from a variety of sources including satellite vegetation indices (such as the Normalized Difference Vegetation Index; NDVI) and atmospheric CO2 measurements. Most of these changes have been attributed to strong warming trends in the northern high latitudes (greater than or equal to 50N). Here we analyze the interannual variation of summer net carbon uptake derived from atmospheric CO2 measurements and satellite NDVI in relation to surface meteorology from regional observational records. We find that increases in spring precipitation and snow pack promote summer net carbon uptake of northern ecosystems independent of air temperature effects. However, satellite NDVI measurements still show an overall benefit of summer photosynthetic activity from regional warming and limited impact of spring precipitation. This discrepancy is attributed to a similar response of photosynthesis and respiration to warming and thus reduced sensitivity of net ecosystem carbon uptake to temperature. Further analysis of boreal tower eddy covariance CO2 flux measurements indicates that summer net carbon uptake is positively correlated with early growing-season surface soil moisture, which is also strongly affected by spring precipitation and snow pack based on analysis of satellite soil moisture retrievals. This is attributed to strong regulation of spring hydrology on soil respiration in relatively wet boreal and arctic ecosystems. These results document the important role of spring hydrology in determining summer net carbon uptake and contrast with prevailing assumptions of dominant cold temperature limitations to high-latitude ecosystems. Our results indicate potentially stronger coupling of boreal/arctic water and carbon cycles with continued regional warming trends.

  11. Assessing the potential long-term increase of oceanic fossil fuel CO2 uptake due to CO2-calcification feedback

    Directory of Open Access Journals (Sweden)

    T. M. Lenton

    2007-07-01

    Full Text Available Plankton manipulation experiments exhibit a wide range of sensitivities of biogenic calcification to simulated anthropogenic acidification of the ocean, with the "lab rat" of planktic calcifiers, Emiliania huxleyi apparently not representative of calcification generally. We assess the implications of this observational uncertainty by creating an ensemble of realizations of an Earth system model that encapsulates a comparable range of uncertainty in calcification response to ocean acidification. We predict that a substantial reduction in marine carbonate production is possible in the future, with enhanced ocean CO2 sequestration across the model ensemble driving a 4–13% reduction in the year 3000 atmospheric fossil fuel CO2 burden. Concurrent changes in ocean circulation and surface temperatures in the model contribute about one third to the increase in CO2 uptake. We find that uncertainty in the predicted strength of CO2-calcification feedback seems to be dominated by the assumption as to which species of calcifier contribute most to carbonate production in the open ocean.

  12. The Hamburg oceanic carbon cycle circulation model. Cycle 1

    International Nuclear Information System (INIS)

    Maier-Reimer, E.; Heinze, C.

    1992-02-01

    The carbon cycle model calculates the prognostic fields of oceanic geochemical carbon cycle tracers making use of a 'frozen' velocity field provided by a run of the LSG oceanic circulation model (see the corresponding manual, LSG=Large Scale Geostrophic). The carbon cycle model includes a crude approximation of interactions between sediment and bottom layer water. A simple (meridionally diffusive) one layer atmosphere model allows to calculate the CO 2 airborne fraction resulting from the oceanic biogeochemical interactions. (orig.)

  13. Trends and regional distributions of land and ocean carbon sinks

    Directory of Open Access Journals (Sweden)

    J. L. Sarmiento

    2010-08-01

    Full Text Available We show here an updated estimate of the net land carbon sink (NLS as a function of time from 1960 to 2007 calculated from the difference between fossil fuel emissions, the observed atmospheric growth rate, and the ocean uptake obtained by recent ocean model simulations forced with reanalysis wind stress and heat and water fluxes. Except for interannual variability, the net land carbon sink appears to have been relatively constant at a mean value of −0.27 Pg C yr−1 between 1960 and 1988, at which time it increased abruptly by −0.88 (−0.77 to −1.04 Pg C yr−1 to a new relatively constant mean of −1.15 Pg C yr−1 between 1989 and 2003/7 (the sign convention is negative out of the atmosphere. This result is detectable at the 99% level using a t-test. The land use source (LU is relatively constant over this entire time interval. While the LU estimate is highly uncertain, this does imply that most of the change in the net land carbon sink must be due to an abrupt increase in the land sink, LS = NLS – LU, in response to some as yet unknown combination of biogeochemical and climate forcing. A regional synthesis and assessment of the land carbon sources and sinks over the post 1988/1989 period reveals broad agreement that the Northern Hemisphere land is a major sink of atmospheric CO2, but there remain major discrepancies with regard to the sign and magnitude of the net flux to and from tropical land.

  14. Observationally-based Metrics of Ocean Carbon and Biogeochemical Variables are Essential for Evaluating Earth System Model Projections

    Science.gov (United States)

    Russell, J. L.; Sarmiento, J. L.

    2017-12-01

    The Southern Ocean is central to the climate's response to increasing levels of atmospheric greenhouse gases as it ventilates a large fraction of the global ocean volume. Global coupled climate models and earth system models, however, vary widely in their simulations of the Southern Ocean and its role in, and response to, the ongoing anthropogenic forcing. Due to its complex water-mass structure and dynamics, Southern Ocean carbon and heat uptake depend on a combination of winds, eddies, mixing, buoyancy fluxes and topography. Understanding how the ocean carries heat and carbon into its interior and how the observed wind changes are affecting this uptake is essential to accurately projecting transient climate sensitivity. Observationally-based metrics are critical for discerning processes and mechanisms, and for validating and comparing climate models. As the community shifts toward Earth system models with explicit carbon simulations, more direct observations of important biogeochemical parameters, like those obtained from the biogeochemically-sensored floats that are part of the Southern Ocean Carbon and Climate Observations and Modeling project, are essential. One goal of future observing systems should be to create observationally-based benchmarks that will lead to reducing uncertainties in climate projections, and especially uncertainties related to oceanic heat and carbon uptake.

  15. The declining uptake rate of atmospheric CO2 by land and ocean sinks

    Directory of Open Access Journals (Sweden)

    M. R. Raupach

    2014-07-01

    Full Text Available Through 1959–2012, an airborne fraction (AF of 0.44 of total anthropogenic CO2 emissions remained in the atmosphere, with the rest being taken up by land and ocean CO2 sinks. Understanding of this uptake is critical because it greatly alleviates the emissions reductions required for climate mitigation, and also reduces the risks and damages that adaptation has to embrace. An observable quantity that reflects sink properties more directly than the AF is the CO2 sink rate (kS, the combined land–ocean CO2 sink flux per unit excess atmospheric CO2 above preindustrial levels. Here we show from observations that kS declined over 1959–2012 by a factor of about 1 / 3, implying that CO2 sinks increased more slowly than excess CO2. Using a carbon–climate model, we attribute the decline in kS to four mechanisms: slower-than-exponential CO2 emissions growth (~ 35% of the trend, volcanic eruptions (~ 25%, sink responses to climate change (~ 20%, and nonlinear responses to increasing CO2, mainly oceanic (~ 20%. The first of these mechanisms is associated purely with the trajectory of extrinsic forcing, and the last two with intrinsic, feedback responses of sink processes to changes in climate and atmospheric CO2. Our results suggest that the effects of these intrinsic, nonlinear responses are already detectable in the global carbon cycle. Although continuing future decreases in kS will occur under all plausible CO2 emission scenarios, the rate of decline varies between scenarios in non-intuitive ways because extrinsic and intrinsic mechanisms respond in opposite ways to changes in emissions: extrinsic mechanisms cause kS to decline more strongly with increasing mitigation, while intrinsic mechanisms cause kS to decline more strongly under high-emission, low-mitigation scenarios as the carbon–climate system is perturbed further from a near-linear regime.

  16. Robust non-local effects of ocean heat uptake on radiative feedback and subtropical cloud cover

    Science.gov (United States)

    Rose, B. E. J.

    2016-02-01

    Much recent work has pointed to the limitations of the global mean planetary energy budget as a useful diagnostic tool for understanding transient climate response, because the climate sensitivity (or radiative feedback) governing the relationships between ocean heat content, surface temperature and top-of-atmosphere energy imbalance depends sensitively on timescale, spatial pattern and nature of the climate forcing. Progress has been made by treating the slowly-evolving (and spatially complex) pattern of ocean heat uptake as a quasi-equilibrium forcing on the "fast" components of the climate system: the atmospheric radiative-dynamical processes that link air-sea heat exchange to the top-of-atmosphere energy budget. Differences between these feedbacks and those on CO2 radiative forcing can be expressed as an "efficacy" of ocean heat uptake. We use idealized slab ocean GCMs forced by prescribed steady energy sinks limited to specific latitude bands (representing heat exchange with the deep ocean) to quantify how (and why) the efficacy depends on the spatial pattern of ocean heat uptake. By repeating the experiment across several independent GCMs we identify robust and non-robust aspects of the response. We find that the efficacy of sub-polar heat uptake is 3 to 4 times larger than the efficacy of tropical heat uptake. Radiative kernel analysis allows an accurate partition into feedbacks due to temperature, water vapor and clouds. We find large and robust differences in clear-sky lapse rate feedbacks, associated with robust differences in large-scale atmospheric circulation and stratification driven by ocean heat uptake. A more novel and surprising result is the robustness across several independent GCMs of the differences in subtropical low cloud feedback (positive under high-latitude uptake, strongly negative under tropical uptake). We trace these robust differences to thermodynamic constraints associated with lower-tropospheric stability and boundary layer

  17. Ammonium uptake by phytoplankton regulates nitrification in the sunlit ocean.

    Science.gov (United States)

    Smith, Jason M; Chavez, Francisco P; Francis, Christopher A

    2014-01-01

    Nitrification, the microbial oxidation of ammonium to nitrate, is a central part of the nitrogen cycle. In the ocean's surface layer, the process alters the distribution of inorganic nitrogen species available to phytoplankton and produces nitrous oxide. A widely held idea among oceanographers is that nitrification is inhibited by light in the ocean. However, recent evidence that the primary organisms involved in nitrification, the ammonia-oxidizing archaea (AOA), are present and active throughout the surface ocean has challenged this idea. Here we show, through field experiments coupling molecular genetic and biogeochemical approaches, that competition for ammonium with phytoplankton is the strongest regulator of nitrification in the photic zone. During multiday experiments at high irradiance a single ecotype of AOA remained active in the presence of rapidly growing phytoplankton. Over the course of this three day experiment, variability in the intensity of competition with phytoplankton caused nitrification rates to decline from those typical of the lower photic zone (60 nmol L-1 d-1) to those in well-lit layers (ammonium than they are by light itself. This finding advances our ability to model the impact of nitrification on estimates of new primary production, and emphasizes the need to more strongly consider the effects of organismal interactions on nutrient standing stocks and biogeochemical cycling in the surface of the ocean.

  18. Global Land Carbon Uptake from Trait Distributions

    Science.gov (United States)

    Butler, E. E.; Datta, A.; Flores-Moreno, H.; Fazayeli, F.; Chen, M.; Wythers, K. R.; Banerjee, A.; Atkin, O. K.; Kattge, J.; Reich, P. B.

    2016-12-01

    Historically, functional diversity in land surface models has been represented through a range of plant functional types (PFTs), each of which has a single value for all of its functional traits. Here we expand the diversity of the land surface by using a distribution of trait values for each PFT. The data for these trait distributions is from a sub-set of the global database of plant traits, TRY, and this analysis uses three leaf traits: mass based nitrogen and phosphorus content and specific leaf area, which influence both photosynthesis and respiration. The data are extrapolated into continuous surfaces through two methodologies. The first, a categorical method, classifies the species observed in TRY into satellite estimates of their plant functional type abundances - analogous to how traits are currently assigned to PFTs in land surface models. Second, a Bayesian spatial method which additionally estimates how the distribution of a trait changes in accord with both climate and soil covariates. These two methods produce distinct patterns of diversity which are incorporated into a land surface model to estimate how the range of trait values affects the global land carbon budget.

  19. Analysis of the global ocean sampling (GOS) project for trends in iron uptake by surface ocean microbes.

    Science.gov (United States)

    Toulza, Eve; Tagliabue, Alessandro; Blain, Stéphane; Piganeau, Gwenael

    2012-01-01

    Microbial metagenomes are DNA samples of the most abundant, and therefore most successful organisms at the sampling time and location for a given cell size range. The study of microbial communities via their DNA content has revolutionized our understanding of microbial ecology and evolution. Iron availability is a critical resource that limits microbial communities' growth in many oceanic areas. Here, we built a database of 2319 sequences, corresponding to 140 gene families of iron metabolism with a large phylogenetic spread, to explore the microbial strategies of iron acquisition in the ocean's bacterial community. We estimate iron metabolism strategies from metagenome gene content and investigate whether their prevalence varies with dissolved iron concentrations obtained from a biogeochemical model. We show significant quantitative and qualitative variations in iron metabolism pathways, with a higher proportion of iron metabolism genes in low iron environments. We found a striking difference between coastal and open ocean sites regarding Fe(2+) versus Fe(3+) uptake gene prevalence. We also show that non-specific siderophore uptake increases in low iron open ocean environments, suggesting bacteria may acquire iron from natural siderophore-like organic complexes. Despite the lack of knowledge of iron uptake mechanisms in most marine microorganisms, our approach provides insights into how the iron metabolic pathways of microbial communities may vary with seawater iron concentrations.

  20. Carbon isotopes in the ocean model of the Community Earth System Model (CESM1

    Directory of Open Access Journals (Sweden)

    A. Jahn

    2015-08-01

    Full Text Available Carbon isotopes in the ocean are frequently used as paleoclimate proxies and as present-day geochemical ocean tracers. In order to allow a more direct comparison of climate model results with this large and currently underutilized data set, we added a carbon isotope module to the ocean model of the Community Earth System Model (CESM, containing the cycling of the stable isotope 13C and the radioactive isotope 14C. We implemented the 14C tracer in two ways: in the "abiotic" case, the 14C tracer is only subject to air–sea gas exchange, physical transport, and radioactive decay, while in the "biotic" version, the 14C additionally follows the 13C tracer through all biogeochemical and ecological processes. Thus, the abiotic 14C tracer can be run without the ecosystem module, requiring significantly fewer computational resources. The carbon isotope module calculates the carbon isotopic fractionation during gas exchange, photosynthesis, and calcium carbonate formation, while any subsequent biological process such as remineralization as well as any external inputs are assumed to occur without fractionation. Given the uncertainty associated with the biological fractionation during photosynthesis, we implemented and tested three parameterizations of different complexity. Compared to present-day observations, the model is able to simulate the oceanic 14C bomb uptake and the 13C Suess effect reasonably well compared to observations and other model studies. At the same time, the carbon isotopes reveal biases in the physical model, for example, too sluggish ventilation of the deep Pacific Ocean.

  1. Carbon isotopes in the ocean model of the Community Earth System Model (CESM1)

    Science.gov (United States)

    Jahn, A.; Lindsay, K.; Giraud, X.; Gruber, N.; Otto-Bliesner, B. L.; Liu, Z.; Brady, E. C.

    2015-08-01

    Carbon isotopes in the ocean are frequently used as paleoclimate proxies and as present-day geochemical ocean tracers. In order to allow a more direct comparison of climate model results with this large and currently underutilized data set, we added a carbon isotope module to the ocean model of the Community Earth System Model (CESM), containing the cycling of the stable isotope 13C and the radioactive isotope 14C. We implemented the 14C tracer in two ways: in the "abiotic" case, the 14C tracer is only subject to air-sea gas exchange, physical transport, and radioactive decay, while in the "biotic" version, the 14C additionally follows the 13C tracer through all biogeochemical and ecological processes. Thus, the abiotic 14C tracer can be run without the ecosystem module, requiring significantly fewer computational resources. The carbon isotope module calculates the carbon isotopic fractionation during gas exchange, photosynthesis, and calcium carbonate formation, while any subsequent biological process such as remineralization as well as any external inputs are assumed to occur without fractionation. Given the uncertainty associated with the biological fractionation during photosynthesis, we implemented and tested three parameterizations of different complexity. Compared to present-day observations, the model is able to simulate the oceanic 14C bomb uptake and the 13C Suess effect reasonably well compared to observations and other model studies. At the same time, the carbon isotopes reveal biases in the physical model, for example, too sluggish ventilation of the deep Pacific Ocean.

  2. Reviews and syntheses: Hidden forests, the role of vegetated coastal habitats in the ocean carbon budget

    Science.gov (United States)

    Duarte, Carlos M.

    2017-01-01

    Vegetated coastal habitats, including seagrass and macroalgal beds, mangrove forests and salt marshes, form highly productive ecosystems, but their contribution to the global carbon budget remains overlooked, and these forests remain hidden in representations of the global carbon budget. Despite being confined to a narrow belt around the shoreline of the world's oceans, where they cover less than 7 million km2, vegetated coastal habitats support about 1 to 10 % of the global marine net primary production and generate a large organic carbon surplus of about 40 % of their net primary production (NPP), which is either buried in sediments within these habitats or exported away. Large, 10-fold uncertainties in the area covered by vegetated coastal habitats, along with variability about carbon flux estimates, result in a 10-fold bracket around the estimates of their contribution to organic carbon sequestration in sediments and the deep sea from 73 to 866 Tg C yr-1, representing between 3 % and 1/3 of oceanic CO2 uptake. Up to 1/2 of this carbon sequestration occurs in sink reservoirs (sediments or the deep sea) beyond these habitats. The organic carbon exported that does not reach depositional sites subsidizes the metabolism of heterotrophic organisms. In addition to a significant contribution to organic carbon production and sequestration, vegetated coastal habitats contribute as much to carbonate accumulation as coral reefs do. While globally relevant, the magnitude of global carbon fluxes supported by salt-marsh, mangrove, seagrass and macroalgal habitats is declining due to rapid habitat loss, contributing to loss of CO2 sequestration, storage capacity and carbon subsidies. Incorporating the carbon fluxes' vegetated coastal habitats' support into depictions of the carbon budget of the global ocean and its perturbations will improve current representations of the carbon budget of the global ocean.

  3. Ammonium uptake by phytoplankton regulates nitrification in the sunlit ocean.

    Directory of Open Access Journals (Sweden)

    Jason M Smith

    Full Text Available Nitrification, the microbial oxidation of ammonium to nitrate, is a central part of the nitrogen cycle. In the ocean's surface layer, the process alters the distribution of inorganic nitrogen species available to phytoplankton and produces nitrous oxide. A widely held idea among oceanographers is that nitrification is inhibited by light in the ocean. However, recent evidence that the primary organisms involved in nitrification, the ammonia-oxidizing archaea (AOA, are present and active throughout the surface ocean has challenged this idea. Here we show, through field experiments coupling molecular genetic and biogeochemical approaches, that competition for ammonium with phytoplankton is the strongest regulator of nitrification in the photic zone. During multiday experiments at high irradiance a single ecotype of AOA remained active in the presence of rapidly growing phytoplankton. Over the course of this three day experiment, variability in the intensity of competition with phytoplankton caused nitrification rates to decline from those typical of the lower photic zone (60 nmol L-1 d-1 to those in well-lit layers (<1 nmol L-1 d-1. During another set of experiments, nitrification rates exhibited a diel periodicity throughout much of the photic zone, with the highest rates occurring at night when competition with phytoplankton is lowest. Together, the results of our experiments indicate that nitrification rates in the photic zone are more strongly regulated by competition with phytoplankton for ammonium than they are by light itself. This finding advances our ability to model the impact of nitrification on estimates of new primary production, and emphasizes the need to more strongly consider the effects of organismal interactions on nutrient standing stocks and biogeochemical cycling in the surface of the ocean.

  4. Dilution limits dissolved organic carbon utilization in the deep ocean

    NARCIS (Netherlands)

    Arrieta, J.M.; Mayol, E.; Hansman, R.L.; Herndl, G.J.; Dittmar, T.; Duarte, C.M.

    2015-01-01

    Oceanic dissolved organic carbon (DOC) is the second largest reservoir of organic carbon in the biosphere. About 72% of the global DOC inventory is stored in deep oceanic layers for years to centuries, supporting the current view that it consists of materials resistant to microbial degradation. An

  5. Can hydrographic data provide evidence that the rate of oceanic uptake of anthropogenic CO2 is increasing?

    Directory of Open Access Journals (Sweden)

    William Carlisle Thacker

    Full Text Available Predictions of the rate of accumulation of anthropogenic carbon dioxide in the Pacific Ocean near 32°S and 150°W based on the P16 surveys of 1991 and 2005 and on the P06 surveys of 1992 and 2003 underestimate the amount found in the P06 survey of 2009-2010, suggesting an increasing uptake rate. Assuming the accumulation rate to be constant over the two decades, analyses using all five surveys lead to upward revision of the rates based only on the first four. On the other hand, accumulation rates estimated for 2003-2010 are significantly greater than those for 1991-2003, again suggesting an increasing uptake rate. In addressing this question it is important to acknowledge the limitations of the repeat hydrography and consequent uncertainties of estimated accumulation rates.

  6. Autonomous observing strategies for the ocean carbon cycle

    Energy Technology Data Exchange (ETDEWEB)

    Bishop, James K.; Davis, Russ E.

    2000-07-26

    Understanding the exchanges of carbon between the atmosphere and ocean and the fate of carbon delivered to the deep sea is fundamental to the evaluation of ocean carbon sequestration options. An additional key requirement is that sequestration must be verifiable and that environmental effects be monitored and minimized. These needs can be addressed by carbon system observations made from low-cost autonomous ocean-profiling floats and gliders. We have developed a prototype ocean carbon system profiler based on the Sounding Oceanographic Lagrangian Observer (SOLO; Davis et al., 1999). The SOLO/ carbon profiler will measure the two biomass components of the carbon system and their relationship to physical variables, such as upper ocean stratification and mixing. The autonomous observations within the upper 1500 m will be made on daily time scales for periods of months to seasons and will be carried out in biologically dynamic locations in the world's oceans that are difficult to access with ships (due to weather) or observe using remote sensing satellites (due to cloud cover). Such an observational capability not only will serve an important role in carbon sequestration research but will provide key observations of the global ocean's natural carbon cycle.

  7. The Seasonal Cycle of Carbon in the Southern Pacific Ocean Observed from Biogeochemical Profiling Floats

    Science.gov (United States)

    Sarmiento, J. L.; Gray, A. R.; Johnson, K. S.; Carter, B.; Riser, S.; Talley, L. D.; Williams, N. L.

    2016-02-01

    The Southern Ocean is thought to play an important role in the ocean-atmosphere exchange of carbon dioxide and the uptake of anthropogenic carbon dioxide. However, the total number of observations of the carbonate system in this region is small and heavily biased towards the summer. Here we present 1.5 years of biogeochemical measurements, including pH, oxygen, and nitrate, collected by 11 autonomous profiling floats deployed in the Pacific sector of the Southern Ocean in April 2014. These floats sampled a variety of oceanographic regimes ranging from the seasonally ice-covered zone to the subtropical gyre. Using an algorithm trained with bottle measurements, alkalinity is estimated from salinity, temperature, and oxygen and then used together with the measured pH to calculate total carbon dioxide and pCO2 in the upper 1500 dbar. The seasonal cycle in the biogeochemical quantities is examined, and the factors governing pCO2 in the surface waters are analyzed. The mechanisms driving the seasonal cycle of carbon are further investigated by computing budgets of heat, carbon, and nitrogen in the mixed layer. Comparing the different regimes sampled by the floats demonstrates the complex and variable nature of the carbon cycle in the Southern Ocean.

  8. Inorganic carbon uptake during photosynthesis. II. Uptake by isolated Asparagus mesophyll cells during isotopic disequilibrium

    International Nuclear Information System (INIS)

    Espie, G.S.; Owttrim, G.W.; Colman, B.

    1986-01-01

    The species of inorganic carbon (CO 2 or HCO 3 - ) taken up as a source of substrate for photosynthetic fixation by isolated Asparagus sprengeri mesophyll cells is investigated. Discrimination between CO 2 or HCO 3 - transport, during steady state photosynthesis, is achieved by monitoring the changes (by 14 C fixation) which occur in the specific activity of the intracellular pool of inorganic carbon when the inorganic carbon present in the suspending medium is in a state of isotopic disequilibrium. Quantitative comparisons between theoretical (CO 2 or HCO 3 - transport) and experimental time-courses of 14 C incorporation, over the pH range of 5.2 to 7.5, indicate that the specific activity of extracellular CO 2 , rather than HCO 3 - , is the appropriate predictor of the intracellular specific activity. It is concluded, therefore, that CO 2 is the major source of exogenous inorganic carbon taken up by Asparagus cells. However, at high pH (8.5), a component of net DIC uptake may be attributable to HCO 3 - transport, as the incorporation of 14 C during isotopic disequilibrium exceeds the maximum possible incorporation predicted on the basis of CO 2 uptake alone. The contribution of HCO 3 - to net inorganic carbon uptake (pH 8.5) is variable, ranging from 5 to 16%, but is independent of the extracellular HCO 3 - concentration. The evidence for direct HCO 3 - transport is subject to alternative explanations and must, therefore, be regarded as equivocal. Nonlinear regression analysis of the rate of 14 C incorporation as a function of time indicates the presence of a small extracellular resistance to the diffusion of CO 2 , which is partially alleviated by a high extracellular concentration of HCO 3 -

  9. Patterns of Seasonal Heat Uptake and Release Over the Arctic Ocean Between 1979-2016

    Science.gov (United States)

    Helmberger, M. N.; Serreze, M. C.

    2017-12-01

    As the Arctic Ocean loses its sea ice cover, there is a stronger oceanic heat gain from the surface fluxes throughout the spring and summer; ultimately meaning that there is more energy to transfer out of the ocean to the atmosphere and outer space in the autumn and winter. Recent work has shown that the increased oceanic heat content at the end of summer in turn delays autumn ice growth, with implications for marine shipping and other economic activities. Some of the autumn and winter heat loss to the atmosphere is represented by evaporation, which increases the atmospheric water vapor content, and there is growing evidence that this is contributing to increases in regional precipitation. However, depending on patterns of seasonal sea ice retreat and weather conditions, the spring-summer heat uptake and autumn-winter heat loss can be highly variable from year to year and regionally. Here, we examine how the seasonality in upper ocean heat uptake and release has evolved over the past 37 years and the relationships between this seasonal heat gain and loss and the evolution of sea ice cover. We determine which regions have seen the largest increases in total seasonal heat uptake and how variable this uptake can be. Has the timing at which the Arctic Ocean (either as a whole or by region) transitions from an atmospheric energy sink to an atmospheric energy source (or from a source to a sink) appreciably changed? What changes have been observed in the seasonal rates of seasonal heat uptake and release? To begin answering these questions, use is made of surface fluxes from the ERA-Interim reanalysis and satellite-derived sea ice extent spanning the period 1979 through the present. Results from ERA-Interim will be compared to those from other reanalyses and satellite-derived flux estimates.

  10. Autonomous observations of the ocean biological carbon pump

    Energy Technology Data Exchange (ETDEWEB)

    Bishop, James K.B.

    2009-03-01

    Prediction of the substantial biologically mediated carbon flows in a rapidly changing and acidifying ocean requires model simulations informed by observations of key carbon cycle processes on the appropriate space and time scales. From 2000 to 2004, the National Oceanographic Partnership Program (NOPP) supported the development of the first low-cost fully-autonomous ocean profiling Carbon Explorers that demonstrated that year-round real-time observations of particulate organic carbon (POC) concentration and sedimentation could be achieved in the world's ocean. NOPP also initiated the development of a sensor for particulate inorganic carbon (PIC) suitable for operational deployment across all oceanographic platforms. As a result, PIC profile characterization that once required shipboard sample collection and shipboard or shore based laboratory analysis, is now possible to full ocean depth in real time using a 0.2W sensor operating at 24 Hz. NOPP developments further spawned US DOE support to develop the Carbon Flux Explorer, a free-vehicle capable of following hourly variations of particulate inorganic and organic carbon sedimentation from near surface to kilometer depths for seasons to years and capable of relaying contemporaneous observations via satellite. We have demonstrated the feasibility of real time - low cost carbon observations which are of fundamental value to carbon prediction and when further developed, will lead to a fully enhanced global carbon observatory capable of real time assessment of the ocean carbon sink, a needed constraint for assessment of carbon management policies on a global scale.

  11. Ocean Fertilization for Sequestration of Carbon Dioxide from the Atmosphere

    Science.gov (United States)

    Boyd, Philip W.

    The ocean is a major sink for both preindustrial and anthropogenic carbon dioxide. Both physically and biogeochemically driven pumps, termed the solubility and biological pump, respectively Fig.5.1) are responsible for the majority of carbon sequestration in the ocean's interior [1]. The solubility pump relies on ocean circulation - specifically the impact of cooling of the upper ocean at high latitudes both enhances the solubility of carbon dioxide and the density of the waters which sink to great depth (the so-called deepwater formation) and thereby sequester carbon in the form of dissolved inorganic carbon (Fig.5.1). The biological pump is driven by the availability of preformed plant macronutrients such as nitrate or phosphate which are taken up by phytoplankton during photosynthetic carbon fixation. A small but significant proportion of this fixed carbon sinks into the ocean's interior in the form of settling particles, and in order to maintain equilibrium carbon dioxide from the atmosphere is transferred across the air-sea interface into the ocean (the so-called carbon drawdown) thereby decreasing atmospheric carbon dioxide (Fig.5.1).Fig.5.1

  12. Macronutrient and carbon supply, uptake and cycling across the Antarctic Peninsula shelf during summer.

    Science.gov (United States)

    Henley, Sian F; Jones, Elizabeth M; Venables, Hugh J; Meredith, Michael P; Firing, Yvonne L; Dittrich, Ribanna; Heiser, Sabrina; Stefels, Jacqueline; Dougans, Julie

    2018-06-28

    The West Antarctic Peninsula shelf is a region of high seasonal primary production which supports a large and productive food web, where macronutrients and inorganic carbon are sourced primarily from intrusions of warm saline Circumpolar Deep Water. We examined the cross-shelf modification of this water mass during mid-summer 2015 to understand the supply of nutrients and carbon to the productive surface ocean, and their subsequent uptake and cycling. We show that nitrate, phosphate, silicic acid and inorganic carbon are progressively enriched in subsurface waters across the shelf, contrary to cross-shelf reductions in heat, salinity and density. We use nutrient stoichiometric and isotopic approaches to invoke remineralization of organic matter, including nitrification below the euphotic surface layer, and dissolution of biogenic silica in deeper waters and potentially shelf sediment porewaters, as the primary drivers of cross-shelf enrichments. Regenerated nitrate and phosphate account for a significant proportion of the total pools of these nutrients in the upper ocean, with implications for the seasonal carbon sink. Understanding nutrient and carbon dynamics in this region now will inform predictions of future biogeochemical changes in the context of substantial variability and ongoing changes in the physical environment.This article is part of the theme issue 'The marine system of the West Antarctic Peninsula: status and strategy for progress in a region of rapid change'. © 2018 The Authors.

  13. Plankton networks driving carbon export in the oligotrophic ocean

    Science.gov (United States)

    Larhlimi, Abdelhalim; Roux, Simon; Darzi, Youssef; Audic, Stephane; Berline, Léo; Brum, Jennifer; Coelho, Luis Pedro; Espinoza, Julio Cesar Ignacio; Malviya, Shruti; Sunagawa, Shinichi; Dimier, Céline; Kandels-Lewis, Stefanie; Picheral, Marc; Poulain, Julie; Searson, Sarah; Stemmann, Lars; Not, Fabrice; Hingamp, Pascal; Speich, Sabrina; Follows, Mick; Karp-Boss, Lee; Boss, Emmanuel; Ogata, Hiroyuki; Pesant, Stephane; Weissenbach, Jean; Wincker, Patrick; Acinas, Silvia G.; Bork, Peer; de Vargas, Colomban; Iudicone, Daniele; Sullivan, Matthew B.; Raes, Jeroen; Karsenti, Eric; Bowler, Chris; Gorsky, Gabriel

    2015-01-01

    The biological carbon pump is the process by which CO2 is transformed to organic carbon via photosynthesis, exported through sinking particles, and finally sequestered in the deep ocean. While the intensity of the pump correlates with plankton community composition, the underlying ecosystem structure driving the process remains largely uncharacterised. Here we use environmental and metagenomic data gathered during the Tara Oceans expedition to improve our understanding of carbon export in the oligotrophic ocean. We show that specific plankton communities, from the surface and deep chlorophyll maximum, correlate with carbon export at 150 m and highlight unexpected taxa such as Radiolaria, alveolate parasites, as well as Synechococcus and their phages, as lineages most strongly associated with carbon export in the subtropical, nutrient-depleted, oligotrophic ocean. Additionally, we show that the relative abundance of just a few bacterial and viral genes can predict most of the variability in carbon export in these regions. PMID:26863193

  14. Plankton networks driving carbon export in the oligotrophic ocean

    Science.gov (United States)

    2016-04-01

    The biological carbon pump is the process by which CO2 is transformed to organic carbon via photosynthesis, exported through sinking particles, and finally sequestered in the deep ocean. While the intensity of the pump correlates with plankton community composition, the underlying ecosystem structure driving the process remains largely uncharacterized. Here we use environmental and metagenomic data gathered during the Tara Oceans expedition to improve our understanding of carbon export in the oligotrophic ocean. We show that specific plankton communities, from the surface and deep chlorophyll maximum, correlate with carbon export at 150 m and highlight unexpected taxa such as Radiolaria and alveolate parasites, as well as Synechococcus and their phages, as lineages most strongly associated with carbon export in the subtropical, nutrient-depleted, oligotrophic ocean. Additionally, we show that the relative abundance of a few bacterial and viral genes can predict a significant fraction of the variability in carbon export in these regions.

  15. Multicentury changes in ocean and land contributions to the climate-carbon feedback

    Science.gov (United States)

    Randerson, J. T.; Lindsay, K.; Munoz, E.; Fu, W.; Moore, J. K.; Hoffman, F. M.; Mahowald, N. M.; Doney, S. C.

    2015-06-01

    Improved constraints on carbon cycle responses to climate change are needed to inform mitigation policy, yet our understanding of how these responses may evolve after 2100 remains highly uncertain. Using the Community Earth System Model (v1.0), we quantified climate-carbon feedbacks from 1850 to 2300 for the Representative Concentration Pathway 8.5 and its extension. In three simulations, land and ocean biogeochemical processes experienced the same trajectory of increasing atmospheric CO2. Each simulation had a different degree of radiative coupling for CO2 and other greenhouse gases and aerosols, enabling diagnosis of feedbacks. In a fully coupled simulation, global mean surface air temperature increased by 9.3 K from 1850 to 2300, with 4.4 K of this warming occurring after 2100. Excluding CO2, warming from other greenhouse gases and aerosols was 1.6 K by 2300, near a 2 K target needed to avoid dangerous anthropogenic interference with the climate system. Ocean contributions to the climate-carbon feedback increased considerably over time and exceeded contributions from land after 2100. The sensitivity of ocean carbon to climate change was found to be proportional to changes in ocean heat content, as a consequence of this heat modifying transport pathways for anthropogenic CO2 inflow and solubility of dissolved inorganic carbon. By 2300, climate change reduced cumulative ocean uptake by 330 Pg C, from 1410 Pg C to 1080 Pg C. Land fluxes similarly diverged over time, with climate change reducing stocks by 232 Pg C. Regional influence of climate change on carbon stocks was largest in the North Atlantic Ocean and tropical forests of South America. Our analysis suggests that after 2100, oceans may become as important as terrestrial ecosystems in regulating the magnitude of the climate-carbon feedback.

  16. Stable carbon isotope response to oceanic anoxic events

    International Nuclear Information System (INIS)

    Hu Xiumian; Wang Chengshan; Li Xianghui

    2001-01-01

    Based on discussion of isotope compositions and fractionation of marine carbonate and organic carbon, the author studies the relationship between oceanic anoxic events and changes in the carbon isotope fractionation of both carbonate and organic matter. During the oceanic anoxic events, a great number of organisms were rapidly buried, which caused a kind of anoxic conditions by their decomposition consuming dissolved oxygen. Since 12 C-rich organism preserved, atmosphere-ocean system will enrich relatively of 13 C. As a result, simultaneous marine carbonate will record the positive excursion of carbon isotope. There is a distinctive δ 13 C excursion during oceanic anoxic events in the world throughout the geological time. In the Cenomanian-Turonian anoxic event. this positive excursion arrived at ∼0.2% of marine carbonate and at ∼0.4% of organic matter, respectively. Variations in the carbon isotopic compositions of marine carbonate and organic carbon record the changes in the fraction of organic carbon buried throughout the geological time and may provide clues to the changes in rates of weathering and burial of organic carbon. This will provide a possibility of interpreting not only the changes in the global carbon cycle throughout the geological time, but also that in atmospheric p CO 2

  17. Marine geochemistry ocean circulation, carbon cycle and climate change

    CERN Document Server

    Roy-Barman, Matthieu

    2016-01-01

    Marine geochemistry uses chemical elements and their isotopes to study how the ocean works. It brings quantitative answers to questions such as: What is the deep ocean mixing rate? How much atmospheric CO2 is pumped by the ocean? How fast are pollutants removed from the ocean? How do ecosystems react to the anthropogenic pressure? The book provides a simple introduction to the concepts (environmental chemistry, isotopes), the methods (field approach, remote sensing, modeling) and the applications (ocean circulation, carbon cycle, climate change) of marine geochemistry with a particular emphasis on isotopic tracers. Marine geochemistry is not an isolated discipline: numerous openings on physical oceanography, marine biology, climatology, geology, pollutions and ecology are proposed and provide a global vision of the ocean. It includes new topics based on ongoing research programs such as GEOTRACES, Global Carbon Project, Tara Ocean. It provides a complete outline for a course in marine geochemistry. To favor a...

  18. Tidal Wetlands and Coastal Ocean Carbon Dynamics

    Science.gov (United States)

    Hopkinson, C.; Wang, S. R.; Forbrich, I.; Giblin, A. E.; Cai, W. J.

    2017-12-01

    Recent overviews of coastal ocean C dynamics have tidal wetlands in a prominent position: a local sink for atmospheric CO2, a local store of OC, and a source of DIC and OC for the adjacent estuary and nearshore ocean. Over the past decade there have been great strides made in quantifying and understanding these flows and linkages. GPP and R of the wetlands are not nearly as imbalanced as thought 30 yrs ago. Heterotrophy of adjacent estuarine waters is not solely due to the respiration of OC exported from the marsh, rather we see the marsh directly respiring into the water during tidal inundation and accumulated marsh DIC draining into tidal creeks. Organic carbon burial on the marsh is still a relatively minor flux, but it is large relative to marsh NEE. Using literature and unpublished data on marsh DIC export, we used examples from Sapelo Island GA USA and Plum Island MA USA to constrain estimates of NEP and potential OC export. P. There remain large uncertainties in quantifying C dynamics of coupled wetland - estuary systems. Gas exchange from the water to atmosphere is one of the largest uncertainties. Work at Sapelo suggests that upwards of 40% of all daily exchange occurs from water flooding the marsh, which is but a few hours a day. This estimate is based on the intercept value for gas exchange vs wind velocity. Another major uncertainty comes from converting between O2 based estimates of metabolism to C. At Sapelo we find PQ and RQ values diverging greatly from Redfield. Finally, C dynamics of the coastal ocean, especially the role of tidal wetlands is likely to change substantially in the future. Studies at Plum Island show a reversal of the 4000 yr process of marsh progradation with marshes eroding away at their edges because of inadequate sediment supply and rising sea level. The fate of eroded OC is questionable. Landward transgression with SLR is the only likely counter to continued wetland loss - but that's a complex social issue requiring new

  19. Comparison of the Carbon System Parameters at the Global CO2 Survey Crossover Locations in the North and South Pacific Ocean, 1990-1996

    Energy Technology Data Exchange (ETDEWEB)

    Feely, Richard A [NOAA, Pacific Marine Environmental Laboratory (PMEL); Lamb, Marilyn F. [NOAA, Pacific Marine Environmental Laboratory (PMEL); Greeley, Dana J. [NOAA, Pacific Marine Environmental Laboratory (PMEL); Wanninkhof, Rik [NOAA, Atlantic Oceanographic and Meteorological Laboratory (AOML)

    1999-10-01

    As a collaborative program to measure global ocean carbon inventories and provide estimates of the anthropogenic carbon dioxide (C02) uptake by the oceans. the National Oceanic and Atmospheric Administration and the U.S. Department of Energy have sponsored the collection of ocean carbon measurements as part of the World Ocean Circulation Experiment and Ocean-Atmosphere Carbon Exchange Study cruises. The cruises discussed here occurred in the North and South Pacific from 1990 through 1996. The carbon parameters from these 30 crossover locations have been compared to ensure that a consistent global data set emerges from the survey cruises. !'he results indicate that for dissolved inorganic carbon. fugacity of C02• and pH. the a~:,rreements at most crossover locations are well within the design specifications for the global CO) survey: whereas. in the case of total alkaliniry. the agreement between crossover locations is not as close.

  20. Major role of marine vegetation on the oceanic carbon cycle

    NARCIS (Netherlands)

    Duarte, C.M.; Middelburg, J.J.; Caraco, N.

    2005-01-01

    The carbon burial in vegetated sediments, ignored in past assessments of carbon burial in the ocean, was evaluated using a bottom-up approach derived from upscaling a compilation of published individual estimates of carbon burial in vegetated habitats (seagrass meadows, salt marshes and mangrove

  1. Green Ocean Amazon 2014/15 – Scaling Amazon Carbon Water Couplings Field Campaign Report

    Energy Technology Data Exchange (ETDEWEB)

    Dubey, Manvendra [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Parket, Harrison [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Myers, Katherine [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Rahn, Thom [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Christoffersson, B. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Wunch, Debra [California Inst. of Technology (CalTech), Pasadena, CA (United States); Wennberg, Paul [California Inst. of Technology (CalTech), Pasadena, CA (United States)

    2016-08-01

    Forests soak up 25% of the carbon dioxide (CO2) emitted by anthropogenic fossil energy use (10 Gt C y-1), moderating its atmospheric accumulation. How this terrestrial CO2 uptake will evolve with climate change in the 21st Century is largely unknown. Rainforests are the most active ecosystems, with the Amazon basin storing 120 Gt C as biomass and exchanging 18 Gt C y-1 of CO2 via photosynthesis and respiration and fixing carbon at 2-3 kg C m-2 y-1. Furthermore, the intense hydrologic and carbon cycles are tightly coupled in the Amazon where about half of the water is recycled by evapotranspiration and the other half imported from the ocean by Northeasterly trade winds. Climate models predict a drying in the Amazon with reduced carbon uptake while observationally guided assessments indicate sustained uptake. We set out to resolve this huge discrepancy in the size and sign of the future Amazon carbon cycle by performing the first simultaneous regional-scale high-frequency measurements of atmospheric CO2, H2O, HOD, CH4, N2O, and CO at the T3 site in Manacupuru, Brazil, as part of DOE's GoAmazon 2014/15 project. Our data will be used to inform and develop DOE's Community Land Model (CLM) on the tropical carbon-water couplings at the appropriate grid scale (10-50 km). Our measurements will also validate the CO2 data from Japan's Greenhouse gases Observing Satellite (GOSAT) and NASA's Orbiting Carbon Observatory (OCO)-2 satellite (launched in July, 2014). Our data addresses these science questions: 1. How does ecosystem heterogeneity and climate variability influence the rainforest carbon cycle? 2. How well do current tropical ecosystem models simulate the observed regional carbon cycle? 3. Does nitrogen deposition (from the Manaus, Brazil, plume) enhance rainforest carbon uptake?

  2. South African integrated carbon observation network (SA-ICON): CO2 measurements on land, atmosphere and ocean

    CSIR Research Space (South Africa)

    Feig, Gregor T

    2016-10-01

    Full Text Available It has become essential to accurately estimate the emission and uptake of atmospheric carbon dioxide (CO(sub2)) around the globe. Atmospheric CO(sub2) plays a central role in the Earth’s atmospheric, ocean and terrestrial systems and it has been...

  3. Role of mesoscale eddies in the global ocean uptake of anthropogenic CO2

    International Nuclear Information System (INIS)

    Zouhair, Lachkar

    2007-02-01

    Mesoscale eddies play a fundamental role in ocean dynamics particularly in the Southern Ocean. Global-scale tracer simulations are typically made at coarse resolution without explicitly modeling eddies. Here we ask what role do eddies play in ocean uptake, storage, and meridional transport of anthropogenic CO 2 , CFC-11 and bomb Δ 14 C. We made global anthropogenic transient tracer simulations in coarse-resolution, ORCA2, and eddy-permitting, ORCA05 and ORCA025, versions of the ocean modelling system NEMO. We focus on the Southern Ocean where tracer air-sea fluxes are largest. Eddies have little effect on bomb Δ 14 C uptake and storage. Yet for CFC-11 and anthropogenic CO 2 , increased eddy activity reduces southern extra-tropical uptake by 28% and 25% respectively, thereby providing better agreement with observations. It is shown that the discrepancies in the equilibration times between the three tracers determine their respective sensitivities to the model horizontal resolution. Applying Gent and McWilliams (1990) (GM) parameterization of eddies in the non-eddying version of the model does improve results, but not enough. An in-depth investigation of the mechanisms by which eddies affect the uptake of the transient tracers shows that including mesoscale eddies leads to an overall reduction in the Antarctic Intermediate Water (AAIW) ventilation, and modifies substantially the spatial distribution of their source regions. This investigation reveals also that the GM parameterization still overestimates the ventilation and the subduction of AAIW in the Indian Ocean where the simulated mixed layer is particularly deep during the winter. This work suggests that most current coarse-resolution models may overestimate the ventilation of AAIW in the Indian sector of the Southern Ocean. This study shows also that the use of the GM parameterization may be of limited utility where mixed layer is relatively deep and confirms the general need for a more adequate

  4. Adsorption uptake of synthetic organic chemicals by carbon nanotubes and activated carbons

    Science.gov (United States)

    Brooks, A. J.; Lim, Hyung-nam; Kilduff, James E.

    2012-07-01

    Carbon nanotubes (CNTs) have shown great promise as high performance materials for adsorbing priority pollutants from water and wastewater. This study compared uptake of two contaminants of interest in drinking water treatment (atrazine and trichloroethylene) by nine different types of carbonaceous adsorbents: three different types of single walled carbon nanotubes (SWNTs), three different sized multi-walled nanotubes (MWNTs), two granular activated carbons (GACs) and a powdered activated carbon (PAC). On a mass basis, the activated carbons exhibited the highest uptake, followed by SWNTs and MWNTs. However, metallic impurities in SWNTs and multiple walls in MWNTs contribute to adsorbent mass but do not contribute commensurate adsorption sites. Therefore, when uptake was normalized by purity (carbon content) and surface area (instead of mass), the isotherms collapsed and much of the CNT data was comparable to the activated carbons, indicating that these two characteristics drive much of the observed differences between activated carbons and CNT materials. For the limited data set here, the Raman D:G ratio as a measure of disordered non-nanotube graphitic components was not a good predictor of adsorption from solution. Uptake of atrazine by MWNTs having a range of lengths and diameters was comparable and their Freundlich isotherms were statistically similar, and we found no impact of solution pH on the adsorption of either atrazine or trichloroethylene in the range of naturally occurring surface water (pH = 5.7-8.3). Experiments were performed using a suite of model aromatic compounds having a range of π-electron energy to investigate the role of π-π electron donor-acceptor interactions on organic compound uptake by SWNTs. For the compounds studied, hydrophobic interactions were the dominant mechanism in the uptake by both SWNTs and activated carbon. However, comparing the uptake of naphthalene and phenanthrene by activated carbon and SWNTs, size exclusion effects

  5. Adsorption uptake of synthetic organic chemicals by carbon nanotubes and activated carbons

    International Nuclear Information System (INIS)

    Brooks, A J; Kilduff, James E; Lim, Hyung-nam

    2012-01-01

    Carbon nanotubes (CNTs) have shown great promise as high performance materials for adsorbing priority pollutants from water and wastewater. This study compared uptake of two contaminants of interest in drinking water treatment (atrazine and trichloroethylene) by nine different types of carbonaceous adsorbents: three different types of single walled carbon nanotubes (SWNTs), three different sized multi-walled nanotubes (MWNTs), two granular activated carbons (GACs) and a powdered activated carbon (PAC). On a mass basis, the activated carbons exhibited the highest uptake, followed by SWNTs and MWNTs. However, metallic impurities in SWNTs and multiple walls in MWNTs contribute to adsorbent mass but do not contribute commensurate adsorption sites. Therefore, when uptake was normalized by purity (carbon content) and surface area (instead of mass), the isotherms collapsed and much of the CNT data was comparable to the activated carbons, indicating that these two characteristics drive much of the observed differences between activated carbons and CNT materials. For the limited data set here, the Raman D:G ratio as a measure of disordered non-nanotube graphitic components was not a good predictor of adsorption from solution. Uptake of atrazine by MWNTs having a range of lengths and diameters was comparable and their Freundlich isotherms were statistically similar, and we found no impact of solution pH on the adsorption of either atrazine or trichloroethylene in the range of naturally occurring surface water (pH = 5.7–8.3). Experiments were performed using a suite of model aromatic compounds having a range of π-electron energy to investigate the role of π–π electron donor–acceptor interactions on organic compound uptake by SWNTs. For the compounds studied, hydrophobic interactions were the dominant mechanism in the uptake by both SWNTs and activated carbon. However, comparing the uptake of naphthalene and phenanthrene by activated carbon and SWNTs, size exclusion

  6. Fugitive carbon dioxide: It's not hiding in the ocean

    International Nuclear Information System (INIS)

    Kerr, R.A.

    1992-01-01

    The fugitive carbon is the difference between the 7 billion or so tons that spew as carbon dioxide from smokestacks and burning tropical forests and the 3.4 billion tons known to stay in the atmosphere. Finding the other 3 billion or 4 billion tons has frustrated researchers for the past 15 years. The oceans certainly take up some of it. Any forecast of global warming has to be based on how much of the carbon dioxide released by human activity will remain in the atmosphere, and predictions vary by 30% depending on the mix of oceanic and terrestrial processes assumed to be removing the gas. What's more, those predictions assume that the processes at work today will go on operating. But not knowing where all the carbon is going raises the unnerving possibility that whatever processes are removing it may soon fall down on the job without warning, accelerating any warming. Such concerns add urgency to the question of whether the ocean harbors the missing carbon. But there's no simple way to find out. The obvious strategy might seem to be to measure the carbon content of the ocean repeatedly to see how much it increases year by year. The trouble is that several billion tons of added carbon, though impressive on a human scale, are undetectable against the huge swings in ocean carbon that occur from season to season, year to year, and place to place

  7. Impact of Idealized Stratospheric Aerosol Injection on the Future Ocean and Land Carbon Cycles

    Science.gov (United States)

    Tjiputra, J.; Lauvset, S.

    2017-12-01

    Using a state-of-the-art Earth system model, we simulate stratospheric aerosol injection (SAI) on top of the Representative Concentration Pathways 8.5 future scenario. Our idealized method prescribes aerosol concentration, linearly increasing from 2020 to 2100, and thereafter remaining constant until 2200. In one of the scenarios, the model able to project future warming below 2 degree toward 2100, despite greatier warming persists in the high latitudes. When SAI is terminated in 2100, a rapid global warming of 0.35 K yr-1 (as compared to 0.05 K yr-1 under RCP8.5) is simulated in the subsequent 10 years, and the global mean temperature rapidly returns to levels close to the reference state. In contrast to earlier findings, we show a weak response in the terrestrial carbon sink during SAI implementation in the 21st century, which we attribute to nitrogen limitation. The SAI increases the land carbon uptake in the temperate forest-, grassland-, and shrub-dominated regions. The resultant lower temperatures lead to a reduction in the heterotrophic respiration rate and increase soil carbon retention. Changes in precipitation patterns are key drivers for variability in vegetation carbon. Upon SAI termination, the level of vegetation carbon storage returns to the reference case, whereas the soil carbon remains high. The ocean absorbs nearly 10% more carbon in the geoengineered simulation than in the reference simulation, leading to a ˜15 ppm lower atmospheric CO2 concentration in 2100. The largest enhancement in uptake occurs in the North Atlantic. In both hemispheres' polar regions, SAI delays the sea ice melting and, consequently, export production remains low. Despite inducing little impact on surface acidification, in the deep water of North Atlantic, SAI-induced circulation changes accelerate the ocean acidification rate and broaden the affected area. Since the deep ocean provides vital ecosystem function and services, e.g., fish stocks, this accelerated changes

  8. Major role of marine vegetation on the oceanic carbon cycle

    Directory of Open Access Journals (Sweden)

    C. M. Duarte

    2005-01-01

    Full Text Available The carbon burial in vegetated sediments, ignored in past assessments of carbon burial in the ocean, was evaluated using a bottom-up approach derived from upscaling a compilation of published individual estimates of carbon burial in vegetated habitats (seagrass meadows, salt marshes and mangrove forests to the global level and a top-down approach derived from considerations of global sediment balance and a compilation of the organic carbon content of vegeatated sediments. Up-scaling of individual burial estimates values yielded a total carbon burial in vegetated habitats of 111 Tmol C y-1. The total burial in unvegetated sediments was estimated to be 126 Tg C y-1, resulting in a bottom-up estimate of total burial in the ocean of about 244 Tg C y-1, two-fold higher than estimates of oceanic carbon burial that presently enter global carbon budgets. The organic carbon concentrations in vegetated marine sediments exceeds by 2 to 10-fold those in shelf/deltaic sediments. Top-down recalculation of ocean sediment budgets to account for these, previously neglected, organic-rich sediments, yields a top-down carbon burial estimate of 216 Tg C y-1, with vegetated coastal habitats contributing about 50%. Even though vegetated carbon burial contributes about half of the total carbon burial in the ocean, burial represents a small fraction of the net production of these ecosystems, estimated at about 3388 Tg C y-1, suggesting that bulk of the benthic net ecosystem production must support excess respiration in other compartments, such as unvegetated sediments and the coastal pelagic compartment. The total excess organic carbon available to be exported to the ocean is estimated at between 1126 to 3534 Tg C y-1, the bulk of which must be respired in the open ocean. Widespread loss of vegetated coastal habitats must have reduced carbon burial in the ocean by about 30 Tg C y-1, identifying the destruction of these ecosystems as an important loss of CO

  9. Audit of the global carbon budget: estimate errors and their impact on uptake uncertainty

    Science.gov (United States)

    Ballantyne, A. P.; Andres, R.; Houghton, R.; Stocker, B. D.; Wanninkhof, R.; Anderegg, W.; Cooper, L. A.; DeGrandpre, M.; Tans, P. P.; Miller, J. B.; Alden, C.; White, J. W. C.

    2015-04-01

    Over the last 5 decades monitoring systems have been developed to detect changes in the accumulation of carbon (C) in the atmosphere and ocean; however, our ability to detect changes in the behavior of the global C cycle is still hindered by measurement and estimate errors. Here we present a rigorous and flexible framework for assessing the temporal and spatial components of estimate errors and their impact on uncertainty in net C uptake by the biosphere. We present a novel approach for incorporating temporally correlated random error into the error structure of emission estimates. Based on this approach, we conclude that the 2σ uncertainties of the atmospheric growth rate have decreased from 1.2 Pg C yr-1 in the 1960s to 0.3 Pg C yr-1 in the 2000s due to an expansion of the atmospheric observation network. The 2σ uncertainties in fossil fuel emissions have increased from 0.3 Pg C yr-1 in the 1960s to almost 1.0 Pg C yr-1 during the 2000s due to differences in national reporting errors and differences in energy inventories. Lastly, while land use emissions have remained fairly constant, their errors still remain high and thus their global C uptake uncertainty is not trivial. Currently, the absolute errors in fossil fuel emissions rival the total emissions from land use, highlighting the extent to which fossil fuels dominate the global C budget. Because errors in the atmospheric growth rate have decreased faster than errors in total emissions have increased, a ~20% reduction in the overall uncertainty of net C global uptake has occurred. Given all the major sources of error in the global C budget that we could identify, we are 93% confident that terrestrial C uptake has increased and 97% confident that ocean C uptake has increased over the last 5 decades. Thus, it is clear that arguably one of the most vital ecosystem services currently provided by the biosphere is the continued removal of approximately half of atmospheric CO2 emissions from the atmosphere

  10. The role of nutricline depth in regulating the ocean carbon cycle.

    Science.gov (United States)

    Cermeño, Pedro; Dutkiewicz, Stephanie; Harris, Roger P; Follows, Mick; Schofield, Oscar; Falkowski, Paul G

    2008-12-23

    Carbon uptake by marine phytoplankton, and its export as organic matter to the ocean interior (i.e., the "biological pump"), lowers the partial pressure of carbon dioxide (pCO(2)) in the upper ocean and facilitates the diffusive drawdown of atmospheric CO(2). Conversely, precipitation of calcium carbonate by marine planktonic calcifiers such as coccolithophorids increases pCO(2) and promotes its outgassing (i.e., the "alkalinity pump"). Over the past approximately 100 million years, these two carbon fluxes have been modulated by the relative abundance of diatoms and coccolithophores, resulting in biological feedback on atmospheric CO(2) and Earth's climate; yet, the processes determining the relative distribution of these two phytoplankton taxa remain poorly understood. We analyzed phytoplankton community composition in the Atlantic Ocean and show that the distribution of diatoms and coccolithophorids is correlated with the nutricline depth, a proxy of nutrient supply to the upper mixed layer of the ocean. Using this analysis in conjunction with a coupled atmosphere-ocean intermediate complexity model, we predict a dramatic reduction in the nutrient supply to the euphotic layer in the coming century as a result of increased thermal stratification. Our findings indicate that, by altering phytoplankton community composition, this causal relationship may lead to a decreased efficiency of the biological pump in sequestering atmospheric CO(2), implying a positive feedback in the climate system. These results provide a mechanistic basis for understanding the connection between upper ocean dynamics, the calcium carbonate-to-organic C production ratio and atmospheric pCO(2) variations on time scales ranging from seasonal cycles to geological transitions.

  11. Reduction in Surface Ocean Carbon Storage across the Middle Miocene

    Science.gov (United States)

    Babila, T. L.; Sosdian, S. M.; Foster, G. L.; Lear, C. H.

    2017-12-01

    During the Middle Miocene, Earth underwent a profound climate shift from the warmth of the Miocene Climatic Optimum (MCO; 14-17 Ma) to the stable icehouse of today during the Middle Miocene Climate transition (MMCT). Elevated atmospheric carbon dioxide concentrations (pCO2) revealed by boron isotope records (δ11B) link massive volcanic outputs of Columbia River Flood Basalts to the general warmth of MCO. Superimposed on the long-term cooling trend (MMCT) is a gradual pCO2 decline and numerous positive carbon isotope (δ13C) excursions that indicate dynamic variations in the global carbon cycle. Enhanced organic carbon burial via marine productivity, increased silicate weathering and volcanic emission cessation are each invoked to explain the drawdown of pCO2. To better constrain the oceanic role in carbon sequestration over the Middle Miocene detailed records of carbonate chemistry are needed. We present high resolution Boron/Calcium (B/Ca) and δ13C records in planktonic foraminifer T.trilobus spanning 12-17 Ma at ODP 761 (tropical eastern Indian Ocean) to document changes in surface ocean carbonate chemistry. An overall 30% increase in B/Ca ratios is expressed as two stepwise phases occurring at 14.7 and 13 Ma. Cyclic B/Ca variations are coherent with complimentary δ13C records suggesting a tight coupling between ocean carbonate chemistry parameters. Lower resolution B/Ca data at DSDP 588 (Pacific) and ODP 926 (Atlantic) corroborate the trends observed at ODP 761. We employ a paired approach that combines B/Ca (this study) to δ11B (Foster et al., 2012) and an ad hoc calibration to estimate changes in surface ocean dissolved inorganic carbon (DIC). We estimate a substantial decrease in surface ocean DIC spanning the Middle Miocene that culminates with modern day like values. This gradual decline in surface ocean DIC is coeval with existing deep-ocean records which together suggests a whole ocean reduction in carbon storage. We speculate that enhanced weathering

  12. Ocean Heat Uptake Slows 21st Century Surface Warming Driven by Extratropical Cloud Feedbacks

    Science.gov (United States)

    Frey, W.; Maroon, E.; Pendergrass, A. G.; Kay, J. E.

    2017-12-01

    Equilibrium climate sensitivity (ECS), the warming in response to instantaneously doubled CO2, has long been used to compare climate models. In many models, ECS is well correlated with warming produced by transient forcing experiments. Modifications to cloud phase at high latitudes in a state-of-the-art climate model, the Community Earth System Model (CESM), produce a large increase in ECS (1.5 K) via extratropical cloud feedbacks. However, only a small surface warming increase occurs in a realistic 21st century simulation including a full-depth dynamic ocean and the "business as usual" RCP8.5 emissions scenario. In fact, the increase in surface warming is only barely above the internal variability-generated range in the CESM Large Ensemble. The small change in 21st century warming is attributed to subpolar ocean heat uptake in both hemispheres. In the Southern Ocean, the mean-state circulation takes up heat while in the North Atlantic a slowdown in circulation acts as a feedback to slow surface warming. These results show the importance of subpolar ocean heat uptake in controlling the pace of warming and demonstrate that ECS cannot be used to reliably infer transient warming when it is driven by extratropical feedbacks.

  13. Enhanced ocean carbon storage from anaerobic alkalinity generation in coastal sediments

    Directory of Open Access Journals (Sweden)

    H. Thomas

    2009-02-01

    Full Text Available The coastal ocean is a crucial link between land, the open ocean and the atmosphere. The shallowness of the water column permits close interactions between the sedimentary, aquatic and atmospheric compartments, which otherwise are decoupled at long time scales (≅ 1000 yr in the open oceans. Despite the prominent role of the coastal oceans in absorbing atmospheric CO2 and transferring it into the deep oceans via the continental shelf pump, the underlying mechanisms remain only partly understood. Evaluating observations from the North Sea, a NW European shelf sea, we provide evidence that anaerobic degradation of organic matter, fuelled from land and ocean, generates total alkalinity (AT and increases the CO2 buffer capacity of seawater. At both the basin wide and annual scales anaerobic AT generation in the North Sea's tidal mud flat area irreversibly facilitates 7–10%, or taking into consideration benthic denitrification in the North Sea, 20–25% of the North Sea's overall CO2 uptake. At the global scale, anaerobic AT generation could be accountable for as much as 60% of the uptake of CO2 in shelf and marginal seas, making this process, the anaerobic pump, a key player in the biological carbon pump. Under future high CO2 conditions oceanic CO2 storage via the anaerobic pump may even gain further relevance because of stimulated ocean productivity.

  14. Anthropogenic perturbation of the carbon fluxes from land to ocean

    KAUST Repository

    Regnier, Pierre

    2013-06-09

    A substantial amount of the atmospheric carbon taken up on land through photosynthesis and chemical weathering is transported laterally along the aquatic continuum from upland terrestrial ecosystems to the ocean. So far, global carbon budget estimates have implicitly assumed that the transformation and lateral transport of carbon along this aquatic continuum has remained unchanged since pre-industrial times. A synthesis of published work reveals the magnitude of present-day lateral carbon fluxes from land to ocean, and the extent to which human activities have altered these fluxes. We show that anthropogenic perturbation may have increased the flux of carbon to inland waters by as much as 1.0 Pg C yr -1 since pre-industrial times, mainly owing to enhanced carbon export from soils. Most of this additional carbon input to upstream rivers is either emitted back to the atmosphere as carbon dioxide (∼0.4 Pg C yr -1) or sequestered in sediments (∼0.5 Pg C yr -1) along the continuum of freshwater bodies, estuaries and coastal waters, leaving only a perturbation carbon input of ∼0.1 Pg C yr -1 to the open ocean. According to our analysis, terrestrial ecosystems store ∼0.9 Pg C yr -1 at present, which is in agreement with results from forest inventories but significantly differs from the figure of 1.5 Pg C yr -1 previously estimated when ignoring changes in lateral carbon fluxes. We suggest that carbon fluxes along the land-ocean aquatic continuum need to be included in global carbon dioxide budgets.

  15. Uptake and retardation of Cl during cement carbonation

    Energy Technology Data Exchange (ETDEWEB)

    Milodowski, A.E.; Rochelle, C.A.; Purser, G. [British Geological Survey, Environmental Science Centre, Keyworth, Nottingham, NG12 5GG (United Kingdom)

    2013-07-01

    The presence of {sup 36}Cl in low- and intermediate-level radioactive waste (L/ILW) is of concern in repository performance assessment. Its mobility and its relatively long half-life (302,000 years) could potentially lead to early release from the waste and its return to the biosphere within the 10{sup 6} timescale. Experiments have been undertaken to examine the impact of carbonation on the mineralogical and physical properties of NRVB cement in relation to the degradation of organic material in the L/ILW, and with oil well Type-G cement in relation to borehole sealing for carbon capture and storage. These show that the cements can uptake a significant amount of Cl through the formation of transient secondary calcium chloroaluminate and Cl-rich calcium silicate hydrate phases. The formation of the Cl-rich phases is enhanced by carbonation reactions and also by low temperatures (20 deg. C). The process may be important in retarding the migration of {sup 36}Cl from a repository for L/ILW. (authors)

  16. Climate, carbon cycling, and deep-ocean ecosystems.

    Science.gov (United States)

    Smith, K L; Ruhl, H A; Bett, B J; Billett, D S M; Lampitt, R S; Kaufmann, R S

    2009-11-17

    Climate variation affects surface ocean processes and the production of organic carbon, which ultimately comprises the primary food supply to the deep-sea ecosystems that occupy approximately 60% of the Earth's surface. Warming trends in atmospheric and upper ocean temperatures, attributed to anthropogenic influence, have occurred over the past four decades. Changes in upper ocean temperature influence stratification and can affect the availability of nutrients for phytoplankton production. Global warming has been predicted to intensify stratification and reduce vertical mixing. Research also suggests that such reduced mixing will enhance variability in primary production and carbon export flux to the deep sea. The dependence of deep-sea communities on surface water production has raised important questions about how climate change will affect carbon cycling and deep-ocean ecosystem function. Recently, unprecedented time-series studies conducted over the past two decades in the North Pacific and the North Atlantic at >4,000-m depth have revealed unexpectedly large changes in deep-ocean ecosystems significantly correlated to climate-driven changes in the surface ocean that can impact the global carbon cycle. Climate-driven variation affects oceanic communities from surface waters to the much-overlooked deep sea and will have impacts on the global carbon cycle. Data from these two widely separated areas of the deep ocean provide compelling evidence that changes in climate can readily influence deep-sea processes. However, the limited geographic coverage of these existing time-series studies stresses the importance of developing a more global effort to monitor deep-sea ecosystems under modern conditions of rapidly changing climate.

  17. Carbon monoxide uptake and the resulting carboxyhemoglobin in man

    Energy Technology Data Exchange (ETDEWEB)

    Hauck, H.; Neuberger, M.

    1984-01-01

    In order to calculate the carboxyhemoglobin concentration in human blood under various circumstances and for particular groups or individuals, the model proposed originally by Coburn and coworkers in a slightly revised form was tested. The relevant breathing parameters were measured as minute averages and used for computation of COHb time course. At the same time blood samples were taken and analyzed for carboxyhemoglobin. For four different subjects, various breathing conditions and work rates the average deviation of experimental data from theoretical predictions is 7.4%. Some data are presented graphically. Excellent conformity of all the results indicate that the model is suitable to show the influence of most physiological and breathing parameters on the dynamics of carbon monxide uptake.

  18. Validation and Intercomparison of Ocean Color Algorithms for Estimating Particulate Organic Carbon in the Oceans

    Directory of Open Access Journals (Sweden)

    Hayley Evers-King

    2017-08-01

    Full Text Available Particulate Organic Carbon (POC plays a vital role in the ocean carbon cycle. Though relatively small compared with other carbon pools, the POC pool is responsible for large fluxes and is linked to many important ocean biogeochemical processes. The satellite ocean-color signal is influenced by particle composition, size, and concentration and provides a way to observe variability in the POC pool at a range of temporal and spatial scales. To provide accurate estimates of POC concentration from satellite ocean color data requires algorithms that are well validated, with uncertainties characterized. Here, a number of algorithms to derive POC using different optical variables are applied to merged satellite ocean color data provided by the Ocean Color Climate Change Initiative (OC-CCI and validated against the largest database of in situ POC measurements currently available. The results of this validation exercise indicate satisfactory levels of performance from several algorithms (highest performance was observed from the algorithms of Loisel et al., 2002; Stramski et al., 2008 and uncertainties that are within the requirements of the user community. Estimates of the standing stock of the POC can be made by applying these algorithms, and yield an estimated mixed-layer integrated global stock of POC between 0.77 and 1.3 Pg C of carbon. Performance of the algorithms vary regionally, suggesting that blending of region-specific algorithms may provide the best way forward for generating global POC products.

  19. Warmer temperatures reduce net carbon uptake, but not water use, in a mature southern Appalachian forest

    Science.gov (United States)

    Increasing air temperature is expected to extend growing season length in temperate, broadleaf forests, leading to potential increases in evapotranspiration and net carbon uptake. However, other key processes affecting water and carbon cycles are also highly temperature-dependent...

  20. Ocean carbon and heat variability in an Earth System Model

    Science.gov (United States)

    Thomas, J. L.; Waugh, D.; Gnanadesikan, A.

    2016-12-01

    Ocean carbon and heat content are very important for regulating global climate. Furthermore, due to lack of observations and dependence on parameterizations, there has been little consensus in the modeling community on the magnitude of realistic ocean carbon and heat content variability, particularly in the Southern Ocean. We assess the differences between global oceanic heat and carbon content variability in GFDL ESM2Mc using a 500-year, pre-industrial control simulation. The global carbon and heat content are directly out of phase with each other; however, in the Southern Ocean the heat and carbon content are in phase. The global heat mutli-decadal variability is primarily explained by variability in the tropics and mid-latitudes, while the variability in global carbon content is primarily explained by Southern Ocean variability. In order to test the robustness of this relationship, we use three additional pre-industrial control simulations using different mesoscale mixing parameterizations. Three pre-industrial control simulations are conducted with the along-isopycnal diffusion coefficient (Aredi) set to constant values of 400, 800 (control) and 2400 m2 s-1. These values for Aredi are within the range of parameter settings commonly used in modeling groups. Finally, one pre-industrial control simulation is conducted where the minimum in the Gent-McWilliams parameterization closure scheme (AGM) increased to 600 m2 s-1. We find that the different simulations have very different multi-decadal variability, especially in the Weddell Sea where the characteristics of deep convection are drastically changed. While the temporal frequency and amplitude global heat and carbon content changes significantly, the overall spatial pattern of variability remains unchanged between the simulations.

  1. Dilution limits dissolved organic carbon utilization in the deep ocean

    KAUST Repository

    Arrieta, Jesus

    2015-03-19

    Oceanic dissolved organic carbon (DOC) is the second largest reservoir of organic carbon in the biosphere. About 72% of the global DOC inventory is stored in deep oceanic layers for years to centuries, supporting the current view that it consists of materials resistant to microbial degradation. An alternative hypothesis is that deep-water DOC consists of many different, intrinsically labile compounds at concentrations too low to compensate for the metabolic costs associated to their utilization. Here, we present experimental evidence showing that low concentrations rather than recalcitrance preclude consumption of a substantial fraction of DOC, leading to slow microbial growth in the deep ocean. These findings demonstrate an alternative mechanism for the long-term storage of labile DOC in the deep ocean, which has been hitherto largely ignored. © 2015, American Association for the Advancement of Science. All rights reserved.

  2. Dilution limits dissolved organic carbon utilization in the deep ocean

    KAUST Repository

    Arrieta, J M; Mayol, Eva; Hansman, Roberta L.; Herndl, Gerhard J.; Dittmar, Thorsten; Duarte, Carlos M.

    2015-01-01

    Oceanic dissolved organic carbon (DOC) is the second largest reservoir of organic carbon in the biosphere. About 72% of the global DOC inventory is stored in deep oceanic layers for years to centuries, supporting the current view that it consists of materials resistant to microbial degradation. An alternative hypothesis is that deep-water DOC consists of many different, intrinsically labile compounds at concentrations too low to compensate for the metabolic costs associated to their utilization. Here, we present experimental evidence showing that low concentrations rather than recalcitrance preclude consumption of a substantial fraction of DOC, leading to slow microbial growth in the deep ocean. These findings demonstrate an alternative mechanism for the long-term storage of labile DOC in the deep ocean, which has been hitherto largely ignored. © 2015, American Association for the Advancement of Science. All rights reserved.

  3. The Ocean Carbon States Database: a proof-of-concept application of cluster analysis in the ocean carbon cycle

    Science.gov (United States)

    Latto, Rebecca; Romanou, Anastasia

    2018-03-01

    In this paper, we present a database of the basic regimes of the carbon cycle in the ocean, the ocean carbon states, as obtained using a data mining/pattern recognition technique in observation-based as well as model data. The goal of this study is to establish a new data analysis methodology, test it and assess its utility in providing more insights into the regional and temporal variability of the marine carbon cycle. This is important as advanced data mining techniques are becoming widely used in climate and Earth sciences and in particular in studies of the global carbon cycle, where the interaction of physical and biogeochemical drivers confounds our ability to accurately describe, understand, and predict CO2 concentrations and their changes in the major planetary carbon reservoirs. In this proof-of-concept study, we focus on using well-understood data that are based on observations, as well as model results from the NASA Goddard Institute for Space Studies (GISS) climate model. Our analysis shows that ocean carbon states are associated with the subtropical-subpolar gyre during the colder months of the year and the tropics during the warmer season in the North Atlantic basin. Conversely, in the Southern Ocean, the ocean carbon states can be associated with the subtropical and Antarctic convergence zones in the warmer season and the coastal Antarctic divergence zone in the colder season. With respect to model evaluation, we find that the GISS model reproduces the cold and warm season regimes more skillfully in the North Atlantic than in the Southern Ocean and matches the observed seasonality better than the spatial distribution of the regimes. Finally, the ocean carbon states provide useful information in the model error attribution. Model air-sea CO2 flux biases in the North Atlantic stem from wind speed and salinity biases in the subpolar region and nutrient and wind speed biases in the subtropics and tropics. Nutrient biases are shown to be most important in

  4. Carbon and its isotopes in mid-oceanic basaltic glasses

    International Nuclear Information System (INIS)

    Des Marais, D.J.

    1984-01-01

    Three carbon components are evident in eleven analyzed mid-oceanic basalts: carbon on sample surfaces (resembling adsorbed gases, organic matter, or other non-magmatic carbon species acquired by the glasses subsequent to their eruption), mantle carbon dioxide in vesicles, and mantle carbon dissolved in the glasses. The combustion technique employed recovered only reduced sulfur, all of which appears to be indigenous to the glasses. The dissolved carbon concentration (measured in vesicle-free glass) increases with the eruption depth of the spreading ridge, and is consistent with earlier data which show that magma carbon solubility increases with pressure. The total glass carbon content (dissolved plus vesicular carbon) may be controlled by the depth of the shallowest ridge magma chamber. Carbon isotopic fractionation accompanies magma degassing; vesicle CO 2 is about 3.8per mille enriched in 13 C, relative to dissolved carbon. Despite this fractionation, delta 13 Csub(PDB) values for all spreading ridge glasses lie within the range -5.6 and -7.5, and the delta 13 Csub(PDB) of mantle carbon likely lies between -5 and -7. The carbon abundances and delta 13 Csub(PDB) values of Kilauea East Rift glasses apparently are influences by the differentiation and movement of magma within that Hawaiian volcano. Using 3 He and carbon data for submarine hydrothermal fluids, the present-day mid-oceanic ridge mantle carbon flux is estimated very roughly to be about 1.0 x 10 13 g C/yr. Such a flux requires 8 Gyr to accumulate the earth's present crustal carbon inventory. (orig.)

  5. The oceanic response to carbon emissions over the next century: investigation using three ocean carbon cycle models

    International Nuclear Information System (INIS)

    Chuck, A.; Tyrrell, T.; Holligan, P.M.; Totterdell, I.J.

    2005-01-01

    A recent study of coupled atmospheric carbon dioxide and the biosphere found alarming sensitivity of next-century atmospheric pCO 2 (and hence planetary temperature) to uncertainties in terrestrial processes. Here we investigate whether there is similar sensitivity associated with uncertainties in the behaviour of the ocean carbon cycle. We investigate this important question using three models of the ocean carbon cycle of varying complexity: (1) a new three-box oceanic carbon cycle model; (2) the HILDA multibox model with high vertical resolution at low latitudes; (3) the Hadley Centre ocean general circulation model (HadOCC). These models were used in combination to assess the quantitative significance (to year 2100 pCO 2 ) of potential changes to the ocean stimulated by global warming and other anthropogenic activities over the period 2000-2100. It was found that an increase in sea surface temperature and a decrease in the mixing rate due to stratification give rise to the greatest relative changes in pCO 2 , both being positive feedbacks. We failed to find any comparable large sensitivity due to the ocean

  6. Carbon Dioxide Emission Pathways Avoiding Dangerous Ocean Impacts

    OpenAIRE

    Kvale, K.; Zickfeld, K.; Bruckner, T.; Meissner, K. J.; Tanaka, K.; Weaver, A. J.

    2012-01-01

    Anthropogenic emissions of greenhouse gases could lead to undesirable effects on oceans in coming centuries. Drawing on recommendations published by the German Advisory Council on Global Change, levels of unacceptable global marine change (so-called guardrails) are defined in terms of global mean temperature, sea level rise, and ocean acidification. A global-mean climate model [the Aggregated Carbon Cycle, Atmospheric Chemistry and Climate Model (ACC2)] is coupled with an economic module [tak...

  7. Highly selective and stable carbon dioxide uptake in polyindole-derived microporous carbon materials.

    Science.gov (United States)

    Saleh, Muhammad; Tiwari, Jitendra N; Kemp, K Christain; Yousuf, Muhammad; Kim, Kwang S

    2013-05-21

    Adsorption with solid sorbents is considered to be one of the most promising methods for the capture of carbon dioxide (CO₂) from power plant flue gases. In this study, microporous carbon materials used for CO₂ capture were synthesized by the chemical activation of polyindole nanofibers (PIF) at temperatures from 500 to 800 °C using KOH, which resulted in nitrogen (N)-doped carbon materials. The N-doped carbon materials were found to be microporous with an optimal adsorption pore size for CO₂ of 0.6 nm and a maximum (Brunauer-Emmett-Teller) BET surface area of 1185 m(2) g(-1). The PIF activated at 600 °C (PIF6) has a surface area of 527 m(2) g(-1) and a maximum CO₂ storage capacity of 3.2 mmol g(-1) at 25 °C and 1 bar. This high CO₂ uptake is attributed to its highly microporous character and optimum N content. Additionally, PIF6 material displays a high CO₂ uptake at low pressure (1.81 mmol g(-1) at 0.2 bar and 25 °C), which is the best low pressure CO₂ uptake reported for carbon-based materials. The adsorption capacity of this material remained remarkably stable even after 10 cycles. The isosteric heat of adsorption was calculated to be in the range of 42.7-24.1 kJ mol(-1). Besides the excellent CO₂ uptake and stability, PIF6 also exhibits high selectivity values for CO₂ over N₂, CH₄, and H₂ of 58.9, 12.3, and 101.1 at 25 °C, respectively, and these values are significantly higher than reported values.

  8. Ocean fertilization, carbon credits and the Kyoto Protocol

    Science.gov (United States)

    Westley, M. B.; Gnanadesikan, A.

    2008-12-01

    Commercial interest in ocean fertilization as a carbon sequestration tool was excited by the December 1997 agreement of the Kyoto Protocol to the United Nations Convention on Climate Change. The Protocol commits industrialized countries to caps on net greenhouse gas emissions and allows for various flexible mechanisms to achieve these caps in the most economically efficient manner possible, including trade in carbon credits from projects that reduce emissions or enhance sinks. The carbon market was valued at 64 billion in 2007, with the bulk of the trading (50 billion) taking place in the highly regulated European Union Emission Trading Scheme, which deals primarily in emission allowances in the energy sector. A much smaller amount, worth $265 million, was traded in the largely unregulated "voluntary" market (Capoor and Ambrosi 2008). As the voluntary market grows, so do calls for its regulation, with several efforts underway to set rules and standards for the sale of voluntary carbon credits using the Kyoto Protocol as a starting point. Four US-based companies and an Australian company currently seek to develop ocean fertilization technologies for the generation of carbon credits. We review these plans through the lens of the Kyoto Protocol and its flexible mechanisms, and examine whether and how ocean fertilization could generate tradable carbon credits. We note that at present, ocean sinks are not included in the Kyoto Protocol, and that furthermore, the Kyoto Protocol only addresses sources and sinks of greenhouse gases within national boundaries, making open-ocean fertilization projects a jurisdictional challenge. We discuss the negotiating history behind the limited inclusion of land use, land use change and forestry in the Kyoto Protocol and the controversy and eventual compromise concerning methodologies for terrestrial carbon accounting. We conclude that current technologies for measuring and monitoring carbon sequestration following ocean fertilization

  9. Carbon availability for the fungus triggers nitrogen uptake and transport in the arbuscular mycorrhizal symbiosis

    Science.gov (United States)

    The arbuscular mycorrhizal (AM) symbiosis is characterized by a transfer of nutrients in exchange for carbon. We tested the effect of the carbon availability for the AM fungus Glomus intraradices on nitrogen (N) uptake and transport in the symbiosis. We followed the uptake and transport of 15N and ...

  10. The Ocean's Carbon Factory: Ocean Composition. The Growth Patterns of Phytoplankton Species

    Science.gov (United States)

    Gregg, Watson

    2000-01-01

    According to biological data recorded by the Sea-Viewing Wide Field-of-View Sensor (SeaWiFS) satellite, the ocean contains nearly half of all the Earth's photosynthesis activity. Through photosynthesis, plant life forms use carbon from the atmosphere, and in return, plants produce the oxygen that life requires. In effect, ocean chlorophyll works like a factory, taking carbon and "manufacturing" the air we breathe. Most ocean-bound photosynthesis is performed by single-celled plants called phytoplankton. "These things are so small," according to Michael Behrenfeld, a researcher at NASA Goddard Space Flight Center, "that if you take hundreds of them and stack them end-to-end, the length of that stack is only the thickness of a penny". The humble phytoplankton species plays a vital role in balancing the amounts of oxygen and carbon dioxide in the atmosphere. Therefore, understanding exactly how phytoplankton growth works is important.

  11. The Ocean Carbon States Database: a proof-of-concept application of cluster analysis in the ocean carbon cycle

    Directory of Open Access Journals (Sweden)

    R. Latto

    2018-03-01

    Full Text Available In this paper, we present a database of the basic regimes of the carbon cycle in the ocean, the ocean carbon states, as obtained using a data mining/pattern recognition technique in observation-based as well as model data. The goal of this study is to establish a new data analysis methodology, test it and assess its utility in providing more insights into the regional and temporal variability of the marine carbon cycle. This is important as advanced data mining techniques are becoming widely used in climate and Earth sciences and in particular in studies of the global carbon cycle, where the interaction of physical and biogeochemical drivers confounds our ability to accurately describe, understand, and predict CO2 concentrations and their changes in the major planetary carbon reservoirs. In this proof-of-concept study, we focus on using well-understood data that are based on observations, as well as model results from the NASA Goddard Institute for Space Studies (GISS climate model. Our analysis shows that ocean carbon states are associated with the subtropical–subpolar gyre during the colder months of the year and the tropics during the warmer season in the North Atlantic basin. Conversely, in the Southern Ocean, the ocean carbon states can be associated with the subtropical and Antarctic convergence zones in the warmer season and the coastal Antarctic divergence zone in the colder season. With respect to model evaluation, we find that the GISS model reproduces the cold and warm season regimes more skillfully in the North Atlantic than in the Southern Ocean and matches the observed seasonality better than the spatial distribution of the regimes. Finally, the ocean carbon states provide useful information in the model error attribution. Model air–sea CO2 flux biases in the North Atlantic stem from wind speed and salinity biases in the subpolar region and nutrient and wind speed biases in the subtropics and tropics. Nutrient biases are shown

  12. Influence of diatom diversity on the ocean biological carbon pump

    Science.gov (United States)

    Tréguer, Paul; Bowler, Chris; Moriceau, Brivaela; Dutkiewicz, Stephanie; Gehlen, Marion; Aumont, Olivier; Bittner, Lucie; Dugdale, Richard; Finkel, Zoe; Iudicone, Daniele; Jahn, Oliver; Guidi, Lionel; Lasbleiz, Marine; Leblanc, Karine; Levy, Marina; Pondaven, Philippe

    2018-01-01

    Diatoms sustain the marine food web and contribute to the export of carbon from the surface ocean to depth. They account for about 40% of marine primary productivity and particulate carbon exported to depth as part of the biological pump. Diatoms have long been known to be abundant in turbulent, nutrient-rich waters, but observations and simulations indicate that they are dominant also in meso- and submesoscale structures such as fronts and filaments, and in the deep chlorophyll maximum. Diatoms vary widely in size, morphology and elemental composition, all of which control the quality, quantity and sinking speed of biogenic matter to depth. In particular, their silica shells provide ballast to marine snow and faecal pellets, and can help transport carbon to both the mesopelagic layer and deep ocean. Herein we show that the extent to which diatoms contribute to the export of carbon varies by diatom type, with carbon transfer modulated by the Si/C ratio of diatom cells, the thickness of the shells and their life strategies; for instance, the tendency to form aggregates or resting spores. Model simulations project a decline in the contribution of diatoms to primary production everywhere outside of the Southern Ocean. We argue that we need to understand changes in diatom diversity, life cycle and plankton interactions in a warmer and more acidic ocean in much more detail to fully assess any changes in their contribution to the biological pump.

  13. Hidden cycle of dissolved organic carbon in the deep ocean.

    Science.gov (United States)

    Follett, Christopher L; Repeta, Daniel J; Rothman, Daniel H; Xu, Li; Santinelli, Chiara

    2014-11-25

    Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ(13)C and age via Δ(14)C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle.

  14. The role of ocean currents for carbonate platform stratigraphy (Invited)

    Science.gov (United States)

    Betzler, C.; Lindhorst, S.; Luedmann, T.; Eberli, G. P.; Reijmer, J.; Huebscher, C. P.

    2013-12-01

    Breaks and turnovers in carbonate bank growth and development record fluctuations in sea-level and environmental changes. For the carbonate banks of the Bahamas, the Maldives, the Queensland, and the Marion Plateau, sea-level changes and synchronous oceanographic and atmospheric circulation events were recorded through compositional and architectural changes. Most of these major carbonate edifices contain drift deposits, indicating that oceanic currents were a major driver of carbonate-bank evolution. It is proposed that such currents have a larger imprint on the growth patterns and the stratigraphic packaging of carbonates than previously thought. In the Bahamas, slope facies of carbonate banks exposed to deep oceanic currents are not arranged into sediment-texture controlled and depth-dependant strike-continuous facies belts. Facies patterns are controlled by the interplay of shallow-water input, succeeding sediment sorting as well as redistribution and erosion processes. This complements the classical windward - leeward classification of carbonate platform slopes and accounts for the significant and potentially dominant process of alongslope sediment transport and dispersal. Deep oceanic currents also have the potential to steepen the carbonate bank slopes, through sediment winnowing at the distal slope, such as for example in the Maldives. This process can be enhanced as the bank grows and expands in size which may accelerate currents. Oceanic current onset or amplification, however, may also account for slope steepening as an externally, i.e. climate-driven agent, thus forcing the banks into an aggradation mode of growth which is not a response to sea-level fluctuations or a result of the windward / leeward exposure of the bank edge. Ignorance of the impact of currents on platforms and platform slopes may lead to an erroneous conclusion that changes in sediment production, distribution, and morphologies of sediment bodies are features solely related to sea

  15. The Ocean Carbon States Database: A Proof-of-Concept Application of Cluster Analysis in the Ocean Carbon Cycle

    Science.gov (United States)

    Latto, Rebecca; Romanou, Anastasia

    2018-01-01

    In this paper, we present a database of the basic regimes of the carbon cycle in the ocean, the 'ocean carbon states', as obtained using a data mining/pattern recognition technique in observation-based as well as model data. The goal of this study is to establish a new data analysis methodology, test it and assess its utility in providing more insights into the regional and temporal variability of the marine carbon cycle. This is important as advanced data mining techniques are becoming widely used in climate and Earth sciences and in particular in studies of the global carbon cycle, where the interaction of physical and biogeochemical drivers confounds our ability to accurately describe, understand, and predict CO2 concentrations and their changes in the major planetary carbon reservoirs. In this proof-of-concept study, we focus on using well-understood data that are based on observations, as well as model results from the NASA Goddard Institute for Space Studies (GISS) climate model. Our analysis shows that ocean carbon states are associated with the subtropical-subpolar gyre during the colder months of the year and the tropics during the warmer season in the North Atlantic basin. Conversely, in the Southern Ocean, the ocean carbon states can be associated with the subtropical and Antarctic convergence zones in the warmer season and the coastal Antarctic divergence zone in the colder season. With respect to model evaluation, we find that the GISS model reproduces the cold and warm season regimes more skillfully in the North Atlantic than in the Southern Ocean and matches the observed seasonality better than the spatial distribution of the regimes. Finally, the ocean carbon states provide useful information in the model error attribution. Model air-sea CO2 flux biases in the North Atlantic stem from wind speed and salinity biases in the subpolar region and nutrient and wind speed biases in the subtropics and tropics. Nutrient biases are shown to be most important

  16. Simulation of anthropogenic CO2 uptake in the CCSM3.1 ocean circulation-biogeochemical model: comparison with data-based estimates

    Directory of Open Access Journals (Sweden)

    S. Khatiwala

    2012-04-01

    Full Text Available The global ocean has taken up a large fraction of the CO2 released by human activities since the industrial revolution. Quantifying the oceanic anthropogenic carbon (Cant inventory and its variability is important for predicting the future global carbon cycle. The detailed comparison of data-based and model-based estimates is essential for the validation and continued improvement of our prediction capabilities. So far, three global estimates of oceanic Cant inventory that are "data-based" and independent of global ocean circulation models have been produced: one based on the Δ C* method, and two that are based on constraining surface-to-interior transport of tracers, the TTD method and a maximum entropy inversion method (GF. The GF method, in particular, is capable of reconstructing the history of Cant inventory through the industrial era. In the present study we use forward model simulations of the Community Climate System Model (CCSM3.1 to estimate the Cant inventory and compare the results with the data-based estimates. We also use the simulations to test several assumptions of the GF method, including the assumption of constant climate and circulation, which is common to all the data-based estimates. Though the integrated estimates of global Cant inventories are consistent with each other, the regional estimates show discrepancies up to 50 %. The CCSM3 model underestimates the total Cant inventory, in part due to weak mixing and ventilation in the North Atlantic and Southern Ocean. Analyses of different simulation results suggest that key assumptions about ocean circulation and air-sea disequilibrium in the GF method are generally valid on the global scale, but may introduce errors in Cant estimates on regional scales. The GF method should also be used with caution when predicting future oceanic anthropogenic carbon uptake.

  17. Controls on thallium uptake during hydrothermal alteration of the upper ocean crust

    Science.gov (United States)

    Coggon, Rosalind M.; Rehkämper, Mark; Atteck, Charlotte; Teagle, Damon A. H.; Alt, Jeffrey C.; Cooper, Matthew J.

    2014-11-01

    Hydrothermal circulation is a fundamental component of global biogeochemical cycles. However, the magnitude of the high temperature axial hydrothermal fluid flux remains disputed, and the lower temperature ridge flank fluid flux is difficult to quantify. Thallium (Tl) isotopes behave differently in axial compared to ridge flank systems, with Tl near-quantitatively stripped from the intrusive crust by high temperature hydrothermal reactions, but added to the lavas during low temperature reaction with seawater. This contrasting behavior provides a unique approach to determine the fluid fluxes associated with axial and ridge flank environments. Unfortunately, our understanding of the Tl isotopic mass balance is hindered by poor knowledge of the mineralogical, physical and chemical controls on Tl-uptake by the ocean crust. Here we use analyses of basaltic volcanic upper crust from Integrated Ocean Drilling Program Hole U1301B on the Juan de Fuca Ridge flank, combined with published analyses of dredged seafloor basalts and upper crustal basalts from Holes 504B and 896A, to investigate the controls on Tl-uptake by mid-ocean ridge basalts and evaluate when in the evolution of the ridge flank hydrothermal system Tl-uptake occurs. Seafloor basalts indicate an association between basaltic uptake of Tl from cold seawater and uptake of Cs and Rb, which are known to partition into K-rich phases. Although there is no clear relationship between Tl and K contents of seafloor basalts, the data do not rule out the incorporation of at least some Tl into the same minerals as the alkali elements. In contrast, we find no relationship between the Tl content and either the abundance of secondary phyllosilicate minerals, or the K, Cs or Rb contents in upper crustal basalts. We conclude that the uptake of Tl and alkali elements during hydrothermal alteration of the upper crust involves different processes and/or mineral phases compared to those that govern seafloor weathering. Furthermore

  18. Can heterotrophic uptake of dissolved organic carbon and zooplankton mitigate carbon budget deficits in annually bleached corals?

    Science.gov (United States)

    Levas, Stephen; Grottoli, Andréa G.; Schoepf, Verena; Aschaffenburg, Matthew; Baumann, Justin; Bauer, James E.; Warner, Mark E.

    2016-06-01

    Annual coral bleaching events due to increasing sea surface temperatures are predicted to occur globally by the mid-century and as early as 2025 in the Caribbean, and severely impact coral reefs. We hypothesize that heterotrophic carbon (C) in the form of zooplankton and dissolved organic carbon (DOC) is a significant source of C to bleached corals. Thus, the ability to utilize multiple pools of fixed carbon and/or increase the amount of fixed carbon acquired from one or more pools of fixed carbon (defined here as heterotrophic plasticity) could underlie coral acclimatization and persistence under future ocean-warming scenarios. Here, three species of Caribbean coral— Porites divaricata, P. astreoides, and Orbicella faveolata—were experimentally bleached for 2.5 weeks in two successive years and allowed to recover in the field. Zooplankton feeding was assessed after single and repeat bleaching, while DOC fluxes and the contribution of DOC to the total C budget were determined after single bleaching, 11 months on the reef, and repeat bleaching. Zooplankton was a large C source for P. astreoides, but only following single bleaching. DOC was a source of C for single-bleached corals and accounted for 11-36 % of daily metabolic demand (CHARDOC), but represented a net loss of C in repeat-bleached corals. In repeat-bleached corals, DOC loss exacerbated the negative C budgets in all three species. Thus, the capacity for heterotrophic plasticity in corals is compromised under annual bleaching, and heterotrophic uptake of DOC and zooplankton does not mitigate C budget deficits in annually bleached corals. Overall, these findings suggest that some Caribbean corals may be more susceptible to repeat bleaching than to single bleaching due to a lack of heterotrophic plasticity, and coral persistence under increasing bleaching frequency may ultimately depend on other factors such as energy reserves and symbiont shuffling.

  19. Assessing carbon dioxide removal through global and regional ocean alkalinization under high and low emission pathways

    Science.gov (United States)

    Lenton, Andrew; Matear, Richard J.; Keller, David P.; Scott, Vivian; Vaughan, Naomi E.

    2018-04-01

    Atmospheric carbon dioxide (CO2) levels continue to rise, increasing the risk of severe impacts on the Earth system, and on the ecosystem services that it provides. Artificial ocean alkalinization (AOA) is capable of reducing atmospheric CO2 concentrations and surface warming and addressing ocean acidification. Here, we simulate global and regional responses to alkalinity (ALK) addition (0.25 PmolALK yr-1) over the period 2020-2100 using the CSIRO-Mk3L-COAL Earth System Model, under high (Representative Concentration Pathway 8.5; RCP8.5) and low (RCP2.6) emissions. While regionally there are large changes in alkalinity associated with locations of AOA, globally we see only a very weak dependence on where and when AOA is applied. On a global scale, while we see that under RCP2.6 the carbon uptake associated with AOA is only ˜ 60 % of the total, under RCP8.5 the relative changes in temperature are larger, as are the changes in pH (140 %) and aragonite saturation state (170 %). The simulations reveal AOA is more effective under lower emissions, therefore the higher the emissions the more AOA is required to achieve the same reduction in global warming and ocean acidification. Finally, our simulated AOA for 2020-2100 in the RCP2.6 scenario is capable of offsetting warming and ameliorating ocean acidification increases at the global scale, but with highly variable regional responses.

  20. Warm ocean processes and carbon cycling in the Eocene.

    Science.gov (United States)

    John, Eleanor H; Pearson, Paul N; Coxall, Helen K; Birch, Heather; Wade, Bridget S; Foster, Gavin L

    2013-10-28

    Sea surface and subsurface temperatures over large parts of the ocean during the Eocene epoch (55.5-33.7 Ma) exceeded modern values by several degrees, which must have affected a number of oceanic processes. Here, we focus on the effect of elevated water column temperatures on the efficiency of the biological pump, particularly in relation to carbon and nutrient cycling. We use stable isotope values from exceptionally well-preserved planktonic foraminiferal calcite from Tanzania and Mexico to reconstruct vertical carbon isotope gradients in the upper water column, exploiting the fact that individual species lived and calcified at different depths. The oxygen isotope ratios of different species' tests are used to estimate the temperature of calcification, which we converted to absolute depths using Eocene temperature profiles generated by general circulation models. This approach, along with potential pitfalls, is illustrated using data from modern core-top assemblages from the same area. Our results indicate that, during the Early and Middle Eocene, carbon isotope gradients were steeper (and larger) through the upper thermocline than in the modern ocean. This is consistent with a shallower average depth of organic matter remineralization and supports previously proposed hypotheses that invoke high metabolic rates in a warm Eocene ocean, leading to more efficient recycling of organic matter and reduced burial rates of organic carbon.

  1. The combined influence of the main European circulation patterns on carbon uptake by ecosystems

    Science.gov (United States)

    Bastos, Ana; Gouveia, Célia; Trigo, Ricardo

    2014-05-01

    Understanding how natural climate variability affects carbon uptake by land and ocean pools is particularly relevant to better characterize human impact on the carbon cycle. Recently, we have contributed to assess the major role played by the El-Niño/Southern Oscillation in driving inter-annual variability (IAV) of carbon uptake by land ecosystems and significantly influencing global CO2 air-borne fraction [1]. Despite the prominent role played by ENSO, other important teleconnections on the hemispheric scale have deserved less attention. On the European scale, the main mode of variability is the North-Atlantic Oscillation (NAO), which controls storm tracks position and drives changes in temperature and precipitation over the whole region, affecting vegetation dynamics [2]. Besides NAO, a few additional large scale circulation patterns the Scandinavian (SC) and East-Atlantic (EA) Patterns, are also known to influence significantly the European climate [3]. Different combinations of these teleconnection polarities have been recently shown to modulate the overall role of the NAO impact location and strength, thus affecting winter temperature and precipitation patterns over Europe [4]. This work aims to answer the following questions: (i) how do NAO, EA and SC affect vegetation carbon uptake IAV? (ii) do the interactions between these three modes have a significant impact on land CO2 IAV? (iii) what is the contribution of the different physical variables to ecosystems' response to these modes? (iv) how well do the state-of-the-art Earth System Models (ESMs) from CMIP5 represent these climate variability modes and the corresponding carbon fluxes? We first analyze observational data to assess the relationships between the different combinations of NAO, SC and EA polarities and IAV of gross and net primary production (GPP and NPP, respectively), as well as the most relevant driving factors of ecosystem's response to those variability patterns. Although the winter state

  2. Pelagic community production and carbon-nutrient stoichiometry under variable ocean acidification in an Arctic fjord

    Directory of Open Access Journals (Sweden)

    A. Silyakova

    2013-07-01

    Full Text Available Net community production (NCP and carbon to nutrient uptake ratios were studied during a large-scale mesocosm experiment on ocean acidification in Kongsfjorden, western Svalbard, during June–July 2010. Nutrient depleted fjord water with natural plankton assemblages, enclosed in nine mesocosms of ~ 50 m3 in volume, was exposed to pCO2 levels ranging initially from 185 to 1420 μatm. NCP estimations are the cumulative change in dissolved inorganic carbon concentrations after accounting for gas exchange and total alkalinity variations. Stoichiometric coupling between inorganic carbon and nutrient net uptake is shown as a ratio of NCP to a cumulative change in inorganic nutrients. Phytoplankton growth was stimulated by nutrient addition half way through the experiment and three distinct peaks in chlorophyll a concentration were observed during the experiment. Accordingly, the experiment was divided in three phases. Cumulative NCP was similar in all mesocosms over the duration of the experiment. However, in phases I and II, NCP was higher and in phase III lower at elevated pCO2. Due to relatively low inorganic nutrient concentration in phase I, C : N and C : P uptake ratios were calculated only for the period after nutrient addition (phase II and phase III. For the total post-nutrient period (phase II + phase III ratios were close to Redfield, however they were lower in phase II and higher in phase III. Variability of NCP, C : N and C : P uptake ratios in different phases reflects the effect of increasing CO2 on phytoplankton community composition and succession. The phytoplankton community was composed predominantly of haptophytes in phase I, prasinophytes, dinoflagellates, and cryptophytes in phase II, and haptophytes, prasinophytes, dinoflagellates and chlorophytes in phase III (Schulz et al., 2013. Increasing ambient inorganic carbon concentrations have also been shown to promote primary production and carbon assimilation. For this study, it is

  3. Can frequent precipitation moderate drought impact on peatmoss carbon uptake in northern peatlands?

    Science.gov (United States)

    Nijp, Jelmer; Limpens, Juul; Metselaar, Klaas; van der Zee, Sjoerd; Berendse, Frank; Robroek, Bjorn

    2014-05-01

    Northern peatlands represent one of the largest global carbon stores that can potentially be released by water table drawdown during extreme summer droughts. Small precipitation events may moderate negative impacts of deep water levels on carbon uptake by sustaining photosynthesis of peatmoss (Sphagnum spp.), the key species in these ecosystems. We experimentally assessed the importance of the temporal distribution of precipitation for Sphagnum water supply and carbon uptake during a stepwise decrease in water levels in a growth chamber. CO2 exchange and the water balance were measured for intact cores of three peatmoss species representative of three contrasting habitats in northern peatlands (Sphagnum fuscum, S. balticum and S. majus). For shallow water levels, capillary rise was the most important source of water for peatmoss photosynthesis and precipitation did not promote carbon uptake irrespective of peatmoss species. For deep water levels, however, precipitation dominated over capillary rise and moderated adverse effects of drought on carbon uptake by peat mosses. The ability to use the transient water supply by precipitation was species-specific: carbon uptake of S. fuscum increased linearly with precipitation frequency for deep water levels, whereas S. balticum and S. majus showed depressed carbon uptake at intermediate precipitation frequencies. Our results highlight the importance of precipitation for carbon uptake by peatmosses. The potential of precipitation to moderate drought impact, however, is species specific and depends on the temporal distribution of precipitation and water level. These results also suggest that modelling approaches in which water level depth is used as the only state variable determining water availability in the living moss layer and (in)directly linked to Sphagnum carbon uptake may have serious drawbacks. The predictive power of peatland ecosystem models may be reduced when deep water levels prevail, as precipitation

  4. Benthic Oxygen Uptake in the Arctic Ocean Margins - A Case Study at the Deep-Sea Observatory HAUSGARTEN (Fram Strait.

    Directory of Open Access Journals (Sweden)

    Cecile Cathalot

    Full Text Available The past decades have seen remarkable changes in the Arctic, a hotspot for climate change. Nevertheless, impacts of such changes on the biogeochemical cycles and Arctic marine ecosystems are still largely unknown. During cruises to the deep-sea observatory HAUSGARTEN in July 2007 and 2008, we investigated the biogeochemical recycling of organic matter in Arctic margin sediments by performing shipboard measurements of oxygen profiles, bacterial activities and biogenic sediment compounds (pigment, protein, organic carbon, and phospholipid contents. Additional in situ oxygen profiles were performed at two sites. This study aims at characterizing benthic mineralization activity along local bathymetric and latitudinal transects. The spatial coverage of this study is unique since it focuses on the transition from shelf to Deep Ocean, and from close to the ice edge to more open waters. Biogeochemical recycling across the continental margin showed a classical bathymetric pattern with overall low fluxes except for the deepest station located in the Molloy Hole (5500 m, a seafloor depression acting as an organic matter depot center. A gradient in benthic mineralization rates arises along the latitudinal transect with clearly higher values at the southern stations (average diffusive oxygen uptake of 0.49 ± 0.18 mmol O2 m-2 d-1 compared to the northern sites (0.22 ± 0.09 mmol O2 m-2 d-1. The benthic mineralization activity at the HAUSGARTEN observatory thus increases southward and appears to reflect the amount of organic matter reaching the seafloor rather than its lability. Although organic matter content and potential bacterial activity clearly follow this gradient, sediment pigments and phospholipids exhibit no increase with latitude whereas satellite images of surface ocean chlorophyll a indicate local seasonal patterns of primary production. Our results suggest that predicted increases in primary production in the Arctic Ocean could induce a larger

  5. Involvement of H(+)-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis.

    Science.gov (United States)

    Furla, P; Allemand, D; Orsenigo, M N

    2000-04-01

    Symbiotic cnidarians absorb inorganic carbon from seawater to supply intracellular dinoflagellates with CO(2) for their photosynthesis. To determine the mechanism of inorganic carbon transport by animal cells, we used plasma membrane vesicles prepared from ectodermal cells isolated from tentacles of the sea anemone, Anemonia viridis. H(14)CO(-)(3) uptake in the presence of an outward NaCl gradient or inward H(+) gradient, showed no evidence for a Cl(-)- or H(+)- driven HCO(-)(3) transport. H(14)CO(-)(3) and (36)Cl(-) uptakes were stimulated by a positive inside-membrane diffusion potential, suggesting the presence of HCO(-)(3) and Cl(-) conductances. A carbonic anhydrase (CA) activity was measured on plasma membrane (4%) and in the cytoplasm of the ectodermal cells (96%) and was sensitive to acetazolamide (IC(50) = 20 nM) and ethoxyzolamide (IC(50) = 2.5 nM). A strong DIDS-sensitive H(+)-ATPase activity was observed (IC(50) = 14 microM). This activity was also highly sensitive to vanadate and allyl isothiocyanate, two inhibitors of P-type H(+)-ATPases. Present data suggest that HCO(-)(3) absorption by ectodermal cells is carried out by H(+) secretion by H(+)-ATPase, resulting in the formation of carbonic acid in the surrounding seawater, which is quickly dehydrated into CO(2) by a membrane-bound CA. CO(2) then diffuses passively into the cell where it is hydrated in HCO(-)(3) by a cytosolic CA.

  6. Effect of membrane on carbonation and carbon dioxide uptake of Chlorella sp.

    Directory of Open Access Journals (Sweden)

    Suali Emma

    2017-01-01

    Full Text Available Recent studies showed that as low as 5% CO2 increased microalgae growth. However, common bioreactor operation resulted in low carbonation due to poor CO2 mass transfer and this inhibited CO2 uptake of microalgae. Although bubbling increases mass transfer of CO2-O2 exchange, preserving high dissolved CO2 remains the most challenging of microalgae cultivation in bioreactor. In order to increase high dissolved CO2 and CO2-O2 exchange, this study employed two types of membrane; hollow-fibre membrane for carbonation and hydrophobic membrane for deoxygenation. It was found that membrane increased carbonation from 20 % to 75 % when operated at control CO2 concentration. The hollow-fibre membrane capable of creating as small as 2 mm bubble which effective for high carbonation. At the same time, itincreased CO2 uptake up to 85% in bioreactor. The hydrophobic membrane removed 43% O2 from the bioreactor. Both membranes increased mass transfer of CO2-O2 exchange in bioreactor which stimulated microalgae growth.

  7. Carbonate preservation during the 'mystery interval' in the northern Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Naik, S.S.; Naidu, P.D.

    maximum is a feature noted across the world oceans and considered to signify carbonate preservation, although it is missing from many sediment cores from the eastern equatorial Pacific, tropical Atlantic and subtropical Indian Ocean The carbonate...

  8. Measuring coral calcification under ocean acidification: methodological considerations for the 45Ca-uptake and total alkalinity anomaly technique

    Directory of Open Access Journals (Sweden)

    Stephanie Cohen

    2017-09-01

    Full Text Available As the oceans become less alkaline due to rising CO2 levels, deleterious consequences are expected for calcifying corals. Predicting how coral calcification will be affected by on-going ocean acidification (OA requires an accurate assessment of CaCO3 deposition and an understanding of the relative importance that decreasing calcification and/or increasing dissolution play for the overall calcification budget of individual corals. Here, we assessed the compatibility of the 45Ca-uptake and total alkalinity (TA anomaly techniques as measures of gross and net calcification (GC, NC, respectively, to determine coral calcification at pHT 8.1 and 7.5. Considering the differing buffering capacity of seawater at both pH values, we were also interested in how strongly coral calcification alters the seawater carbonate chemistry under prolonged incubation in sealed chambers, potentially interfering with physiological functioning. Our data indicate that NC estimates by TA are erroneously ∼5% and ∼21% higher than GC estimates from 45Ca for ambient and reduced pH, respectively. Considering also previous data, we show that the consistent discrepancy between both techniques across studies is not constant, but largely depends on the absolute value of CaCO3 deposition. Deriving rates of coral dissolution from the difference between NC and GC was not possible and we advocate a more direct approach for the future by simultaneously measuring skeletal calcium influx and efflux. Substantial changes in carbonate system parameters for incubation times beyond two hours in our experiment demonstrate the necessity to test and optimize experimental incubation setups when measuring coral calcification in closed systems, especially under OA conditions.

  9. EPOCA/EUR-OCEANS data compilation on the biological and biogeochemical responses to ocean acidification

    NARCIS (Netherlands)

    Nisumaa, A.-M.; Pesant, S.; Bellerby, R.G.J.; Delille, B.; Middelburg, J.J.; Orr, J.C.; Riebesell, U.; Tyrrell, T.; Wolf-Gladrow, D.; Gattuso, J.P.

    2010-01-01

    The uptake of anthropogenic CO2 by the oceans has led to a rise in the oceanic partial pressure of CO2, and to a decrease in pH and carbonate ion concentration. This modification of the marine carbonate system is referred to as ocean acidification. Numerous papers report the effects of ocean

  10. Dissolved organic carbon pools and export from the coastal ocean

    KAUST Repository

    Barrón, Cristina

    2015-10-21

    The distribution of dissolved organic carbon (DOC) concentration across coastal waters was characterized based on the compilation of 3510 individual estimates of DOC in coastal waters worldwide. We estimated the DOC concentration in the coastal waters that directly exchange with open ocean waters in two different ways, as the DOC concentration at the edge of the shelf break and as the DOC concentration in coastal waters with salinity close to the average salinity in the open ocean. Using these estimates of DOC concentration in the coastal waters that directly exchange with open ocean waters, the mean DOC concentration in the open ocean and the estimated volume of water annually exchanged between coastal and open ocean, we estimated a median ± SE (and average ± SE) global DOC export from coastal to open ocean waters ranging from 4.4 ± 1.0 Pg C yr−1 to 27.0 ± 1.8 Pg C yr−1 (7.0 ± 5.8 Pg C yr−1 to 29.0 ± 8.0 Pg C yr−1) depending on the global hydrological exchange. These values correspond to a median and mean median (and average) range between 14.7 ± 3.3 to 90.0 ± 6.0 (23.3 ± 19.3 to 96.7 ± 26.7) Gg C yr−1 per km of shelf break, which is consistent with the range between 1.4 to 66.1 Gg C yr−1 per km of shelf break of available regional estimates of DOC export. The estimated global DOC export from coastal to open ocean waters is also consistent with independent estimates of the net metabolic balance of the coastal ocean. The DOC export from the coastal to the open ocean is likely to be a sizeable flux and is likely to be an important term in the carbon budget of the open ocean, potentially providing an important subsidy to support heterotrophic activity in the open ocean.

  11. Dissolved organic carbon pools and export from the coastal ocean

    KAUST Repository

    Barró n, Cristina; Duarte, Carlos M.

    2015-01-01

    The distribution of dissolved organic carbon (DOC) concentration across coastal waters was characterized based on the compilation of 3510 individual estimates of DOC in coastal waters worldwide. We estimated the DOC concentration in the coastal waters that directly exchange with open ocean waters in two different ways, as the DOC concentration at the edge of the shelf break and as the DOC concentration in coastal waters with salinity close to the average salinity in the open ocean. Using these estimates of DOC concentration in the coastal waters that directly exchange with open ocean waters, the mean DOC concentration in the open ocean and the estimated volume of water annually exchanged between coastal and open ocean, we estimated a median ± SE (and average ± SE) global DOC export from coastal to open ocean waters ranging from 4.4 ± 1.0 Pg C yr−1 to 27.0 ± 1.8 Pg C yr−1 (7.0 ± 5.8 Pg C yr−1 to 29.0 ± 8.0 Pg C yr−1) depending on the global hydrological exchange. These values correspond to a median and mean median (and average) range between 14.7 ± 3.3 to 90.0 ± 6.0 (23.3 ± 19.3 to 96.7 ± 26.7) Gg C yr−1 per km of shelf break, which is consistent with the range between 1.4 to 66.1 Gg C yr−1 per km of shelf break of available regional estimates of DOC export. The estimated global DOC export from coastal to open ocean waters is also consistent with independent estimates of the net metabolic balance of the coastal ocean. The DOC export from the coastal to the open ocean is likely to be a sizeable flux and is likely to be an important term in the carbon budget of the open ocean, potentially providing an important subsidy to support heterotrophic activity in the open ocean.

  12. Increasing efficiency of CO2 uptake by combined land-ocean sink

    Science.gov (United States)

    van Marle, M.; van Wees, D.; Houghton, R. A.; Nassikas, A.; van der Werf, G.

    2017-12-01

    Carbon-climate feedbacks are one of the key uncertainties in predicting future climate change. Such a feedback could originate from carbon sinks losing their efficiency, for example due to saturation of the CO2 fertilization effect or ocean warming. An indirect approach to estimate how the combined land and ocean sink responds to climate change and growing fossil fuel emissions is based on assessing the trends in the airborne fraction of CO2 emissions from fossil fuel and land use change. One key limitation with this approach has been the large uncertainty in quantifying land use change emissions. We have re-assessed those emissions in a more data-driven approach by combining estimates coming from a bookkeeping model with visibility-based land use change emissions available for the Arc of Deforestation and Equatorial Asia, two key regions with large land use change emissions. The advantage of the visibility-based dataset is that the emissions are observation-based and this dataset provides more detailed information about interannual variability than previous estimates. Based on our estimates we provide evidence that land use and land cover change emissions have increased more rapidly than previously thought, implying that the airborne fraction has decreased since the start of CO2 measurements in 1959. This finding is surprising because it means that the combined land and ocean sink has become more efficient while the opposite is expected.

  13. Carbonate-silicate cycle models of the long-term carbon cycle, carbonate accumulation in the oceans, and climate

    International Nuclear Information System (INIS)

    Caldeira, K.G.

    1991-01-01

    Several models of the long-term carbon cycle, incorporating models of the carbonate-silicate cycle, were developed and utilized to investigate issues relating to global climate and the causes and consequences of changes in calcium carbonate accumulation in the oceans. Model results indicate that the marked mid-Cretaceous (120 Ma) global warming could be explained by increased rates of release of carbon dioxide from subduction-zone metamorphism and mid-ocean-ridges, in conjunction with paleogeographic factors. Since the mid-Cretaceous, the primary setting for calcium carbonate accumulation in the oceans has shifted from shallow-water to deep-water environments. Model results suggest that this shift could have major consequences for the carbonate-silicate cycle and climate, and lead to significant increases in the flux of metamorphic carbon dioxide to the atmosphere. Increases in pelagic carbonate productivity, and decreases in tropical shallow-water area available for neritic carbonate accumulation, have both been proposed as the primary cause of this shift. Two lines of evidence developed here (one involving a statistical analysis of Tertiary carbonate-accumulation and oxygen-isotope data, and another based on modeling the carbonate-silicate cycle and ocean chemistry) suggest that a decrease in tropical shallow-water area was more important than increased pelagic productivity in explaining this shift. Model investigations of changes in ocean chemistry at the Cretaceous/Tertiary (K/T) boundary (66 Ma) indicate that variations in deep-water carbonate productivity may affect shallow-water carbonate accumulation rates through a mechanism involving surface-water carbonate-ion concentration. In the aftermath of the K/T boundary event, deep-water carbonate production and accumulation were significantly reduced as a result of the extinction of calcareous plankton

  14. Irreversible ocean thermal expansion under carbon dioxide removal

    Science.gov (United States)

    Ehlert, Dana; Zickfeld, Kirsten

    2018-03-01

    In the Paris Agreement in 2015 countries agreed on holding global mean surface air warming to well below 2 °C above pre-industrial levels, but the emission reduction pledges under that agreement are not ambitious enough to meet this target. Therefore, the question arises of whether restoring global warming to this target after exceeding it by artificially removing CO2 from the atmosphere is possible. One important aspect is the reversibility of ocean heat uptake and associated sea level rise, which have very long (centennial to millennial) response timescales. In this study the response of sea level rise due to thermal expansion to a 1 % yearly increase of atmospheric CO2 up to a quadrupling of the pre-industrial concentration followed by a 1 % yearly decline back to the pre-industrial CO2 concentration is examined using the University of Victoria Earth System Climate Model (UVic ESCM). We find that global mean thermosteric sea level (GMTSL) continues to rise for several decades after atmospheric CO2 starts to decline and does not return to pre-industrial levels for over 1000 years after atmospheric CO2 is restored to the pre-industrial concentration. This finding is independent of the strength of vertical sub-grid-scale ocean mixing implemented in the model. Furthermore, GMTSL rises faster than it declines in response to a symmetric rise and decline in atmospheric CO2 concentration partly because the deep ocean continues to warm for centuries after atmospheric CO2 returns to the pre-industrial concentration. Both GMTSL rise and decline rates increase with increasing vertical ocean mixing. Exceptions from this behaviour arise if the overturning circulations in the North Atlantic and Southern Ocean intensify beyond pre-industrial levels in model versions with lower vertical mixing, which leads to rapid cooling of the deep ocean.

  15. Impact of sinking carbon flux on accumulation of deep-ocean carbon in the Northern Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Sarma, V.V.S.S.; DileepKumar, M.; Saino, T.

    calculations using 14 C activity arises from the separation of natural 90 Biogeochemistry (2007) 82:89–100 123 and bomb-produced 14 C. Rubin and Key (2002) proposed the potential alkalinity method to achieve the separation. However, they found anomalous scatter... in the relationship between 14 C and potential alkalinity caused by data from the northern Indian Ocean (north of equator) and attributed that to the possible transportation of bomb radiocarbon, as carbonate particles from the surface ocean to the sediment...

  16. Southern Ocean Carbon Dioxide and Oxygen Fluxes Detected by SOCCOM Biogeochemical Profiling Floats

    Science.gov (United States)

    Sarmiento, J. L.; Bushinksy, S.; Gray, A. R.

    2016-12-01

    The Southern Ocean is known to play an important role in the global carbon cycle, yet historically our measurements of this remote region have been sparse and heavily biased towards summer. Here we present new estimates of air-sea fluxes of carbon dioxide and oxygen calculated with measurements from autonomous biogeochemical profiling floats. At high latitudes in and southward of the Antarctic Circumpolar Current, we find a significant flux of CO2 from the ocean to the atmosphere during 2014-2016, which is particularly enhanced during winter months. These results suggest that previous estimates may be biased towards stronger Southern Ocean CO2 uptake due to undersampling in winter. We examine various implications of having a source of CO2 that is higher than previous estimates. We also find that CO2:O2 flux ratios north of the Subtropical Front are positive, consistent with the fluxes being driven by changes in solubility, while south of the Polar Front biological processes and upwelling of deep water combine to produce a negative CO2:O2 flux ratio.

  17. Photo-lability of deep ocean dissolved black carbon

    Directory of Open Access Journals (Sweden)

    A. Stubbins

    2012-05-01

    Full Text Available Dissolved black carbon (DBC, defined here as condensed aromatics isolated from seawater via PPL solid phase extraction and quantified as benzenepolycarboxylic acid (BPCA oxidation products, is a significant component of the oceanic dissolved organic carbon (DOC pool. These condensed aromatics are widely distributed in the open ocean and appear to be tens of thousands of years old. As such DBC is regarded as highly refractory. In the current study, the photo-lability of DBC, DOC and coloured dissolved organic matter (CDOM; ultraviolet-visible absorbance were determined over the course of a 28 day irradiation of North Atlantic Deep Water under a solar simulator. During the irradiation DBC fell from 1044 ± 164 nM-C to 55 ± 15 nM-C, a 20-fold decrease in concentration. Dissolved black carbon photo-degradation was more rapid and more extensive than for bulk CDOM and DOC. The concentration of DBC correlated with CDOM absorbance and the quality of DBC indicated by the ratios of different BPCAs correlated with CDOM absorbance spectral slope, suggesting the optical properties of CDOM may provide a proxy for both DBC concentrations and quality in natural waters. Further, the photo-lability of components of the DBC pool increased with their degree of aromatic condensation. These trends indicate that a continuum of compounds of varying photo-lability exists within the marine DOC pool. In this continuum, photo-lability scales with aromatic character, specifically the degree of condensation. Scaling the rapid photo-degradation of DBC to rates of DOC photo-mineralisation for the global ocean leads to an estimated photo-chemical half-life for oceanic DBC of less than 800 years. This is more than an order of magnitude shorter than the apparent age of DBC in the ocean. Consequently, photo-degradation is posited as the primary sink for oceanic DBC and the apparent survival of DBC molecules in the oceans for millennia appears to be facilitated not by their

  18. Natural variability in the surface ocean carbonate ion concentration

    OpenAIRE

    N. S. Lovenduski; M. C. Long; K. Lindsay

    2015-01-01

    We investigate variability in the surface ocean carbonate ion concentration ([CO32−]) on the basis of a long control simulation with a fully-coupled Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical...

  19. Natural variability in the surface ocean carbonate ion concentration

    OpenAIRE

    Lovenduski, N. S.; Long, M. C.; Lindsay, K.

    2015-01-01

    We investigate variability in the surface ocean carbonate ion concentration ([CO32−]) on the basis of a~long control simulation with an Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical Pacific and ...

  20. Evidence for the role of the Atlantic multidecadal oscillation and the ocean heat uptake in hiatus prediction

    Science.gov (United States)

    Pasini, Antonello; Triacca, Umberto; Attanasio, Alessandro

    2017-08-01

    The recent hiatus in global temperature at the surface has been analysed by several studies, mainly using global climate models. The common accepted picture is that since the late 1990s, the increase in anthropogenic radiative forcings has been counterbalanced by other factors, e.g., a decrease in natural forcings, augmented ocean heat storage and negative phases of ocean-atmosphere-coupled oscillation patterns. Here, simple vector autoregressive models are used for forecasting the temperature hiatus in the period 2001-2014. This gives new insight into the problem of understanding the ocean contribution (in terms of heat uptake and atmosphere-ocean-coupled oscillations) to the appearance of this recent hiatus. In particular, considering data about the ocean heat content until a depth of 700 m and the Atlantic multidecadal oscillation is necessary for correctly forecasting the hiatus, so catching both trend and interannual variability. Our models also show that the ocean heat uptake is substantially driven by the natural component of the total radiative forcing at a decadal time scale, confining the importance of the anthropogenic influences to a longer range warming of the ocean.

  1. CO2 uptake potential due to concrete carbonation: A case study

    Directory of Open Access Journals (Sweden)

    Edna Possan

    2017-06-01

    Full Text Available The cement manufacturing process accounts for about 5% CO2 (carbon dioxide released into the atmosphere. However, during its life cycle, concrete may capture CO2 through carbonation, in order to, partially, offset the impact of its production. Thus, this paper aims at studying the CO2 uptake potential of the Itaipu Dam due to concrete carbonation of such material. So, 155 cores were extracted from the concrete dam in different points to measure carbonation depth. In order to evaluate its influence on carbonation, the measurement of internal moisture distribution in concrete was also carried out. The results have shown that carbonation takes part of the whole dam area, indicating CO2 uptake potential. Up to the present moment, 13,384 tons of CO2 have been absorbed by concrete carbonation of the Itaipu Dam.

  2. Natural variability in the surface ocean carbonate ion concentration

    Directory of Open Access Journals (Sweden)

    N. S. Lovenduski

    2015-11-01

    Full Text Available We investigate variability in the surface ocean carbonate ion concentration ([CO32−] on the basis of a~long control simulation with an Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical Pacific and at the boundaries between the subtropical and subpolar gyres in the Northern Hemisphere, and relatively low interannual variability in the centers of the subtropical gyres and in the Southern Ocean. Statistical analysis of modeled [CO32−] variance and autocorrelation suggests that significant anthropogenic trends in the saturation state of aragonite (Ωaragonite are already or nearly detectable at the sustained, open-ocean time series sites, whereas several decades of observations are required to detect anthropogenic trends in Ωaragonite in the tropical Pacific, North Pacific, and North Atlantic. The detection timescale for anthropogenic trends in pH is shorter than that for Ωaragonite, due to smaller noise-to-signal ratios and lower autocorrelation in pH. In the tropical Pacific, the leading mode of surface [CO32−] variability is primarily driven by variations in the vertical advection of dissolved inorganic carbon (DIC in association with El Niño–Southern Oscillation. In the North Pacific, surface [CO32−] variability is caused by circulation-driven variations in surface DIC and strongly correlated with the Pacific Decadal Oscillation, with peak spectral power at 20–30-year periods. North Atlantic [CO32−] variability is also driven by variations in surface DIC, and exhibits weak correlations with both the North Atlantic Oscillation and the Atlantic Multidecadal Oscillation. As the scientific community seeks to detect the anthropogenic influence on ocean carbonate chemistry, these results

  3. Natural variability in the surface ocean carbonate ion concentration

    Science.gov (United States)

    Lovenduski, N. S.; Long, M. C.; Lindsay, K.

    2015-11-01

    We investigate variability in the surface ocean carbonate ion concentration ([CO32-]) on the basis of a~long control simulation with an Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32-] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32-] in the tropical Pacific and at the boundaries between the subtropical and subpolar gyres in the Northern Hemisphere, and relatively low interannual variability in the centers of the subtropical gyres and in the Southern Ocean. Statistical analysis of modeled [CO32-] variance and autocorrelation suggests that significant anthropogenic trends in the saturation state of aragonite (Ωaragonite) are already or nearly detectable at the sustained, open-ocean time series sites, whereas several decades of observations are required to detect anthropogenic trends in Ωaragonite in the tropical Pacific, North Pacific, and North Atlantic. The detection timescale for anthropogenic trends in pH is shorter than that for Ωaragonite, due to smaller noise-to-signal ratios and lower autocorrelation in pH. In the tropical Pacific, the leading mode of surface [CO32-] variability is primarily driven by variations in the vertical advection of dissolved inorganic carbon (DIC) in association with El Niño-Southern Oscillation. In the North Pacific, surface [CO32-] variability is caused by circulation-driven variations in surface DIC and strongly correlated with the Pacific Decadal Oscillation, with peak spectral power at 20-30-year periods. North Atlantic [CO32-] variability is also driven by variations in surface DIC, and exhibits weak correlations with both the North Atlantic Oscillation and the Atlantic Multidecadal Oscillation. As the scientific community seeks to detect the anthropogenic influence on ocean carbonate chemistry, these results will aid the interpretation of trends

  4. Forest Carbon Uptake and the Fundamental Theorem of Calculus

    Science.gov (United States)

    Zobitz, John

    2013-01-01

    Using the fundamental theorem of calculus and numerical integration, we investigate carbon absorption of ecosystems with measurements from a global database. The results illustrate the dynamic nature of ecosystems and their ability to absorb atmospheric carbon.

  5. A Restricted Boltzman Neural Net to Infer Carbon Uptake from OCO-2 Satellite Data

    Science.gov (United States)

    Halem, M.; Dorband, J. E.; Radov, A.; Barr-Dallas, M.; Gentine, P.

    2015-12-01

    For several decades, scientists have been using satellite observations to infer climate budgets of terrestrial carbon uptake employing inverse methods in conjunction with ecosystem models and coupled global climate models. This is an extremely important Big Data calculation today since the net annual photosynthetic carbon uptake changes annually over land and removes on average ~20% of the emissions from human contributions to atmospheric loading of CO2 from fossil fuels. Unfortunately, such calculations have large uncertainties validated with in-situ networks of measuring stations across the globe. One difficulty in using satellite data for these budget calculations is that the models need to assimilate surface fluxes of CO2 as well as soil moisture, vegatation cover and the eddy covariance of latent and sensible heat to calculate the carbon fixed in the soil while satellite spectral observations only provide near surface concentrations of CO2. In July 2014, NASA successfully launched OCO-2 which provides 3km surface measurements of CO2 over land and oceans. We have collected nearly one year of Level 2 XCO2 data from the OCO-2 satellite for 3 sites of ~200 km2 at equatorial, temperate and high latitudes. Each selected site was part of the Fluxnet or ARM system with tower stations for measuring and collecting CO2 fluxes on an hourly basis, in addition to eddy transports of the other parameters. We are also planning to acquire the 4km NDVI products from MODIS and registering the data to the 3km XCO2 footprints for the three sites. We have implemented a restricted Boltzman machine on the quantum annealing D-Wave computer, a novel deep learning neural net, to be used for training with station data to infer CO2 fluxes from collocated XCO2, MODIS vegetative land cover and MERRA reanalysis surface exchange products. We will present performance assessments of the D-Wave Boltzman machine for generating XCO2 fluxes from the OCO-2 satellite observations for the 3 sites by

  6. Carbon isotopes and concentrations in mid-oceanic ridge basalts

    International Nuclear Information System (INIS)

    Pineau, F.; Javoy, M.

    1983-01-01

    In order to estimate carbon fluxes at mid-ocean ridges and carbon isotopic compositions in the convective mantle, we have studied carbon concentrations and isotopic compositions in tholeiitic glasses from the FAMOUS zone (Mid-Atlantic Ridge at 36 0 N) and East Pacific Rise from 21 0 N (RITA zone) to 20 0 S. These samples correspond essentially to the whole spectrum of spreading rates (2-16 cm/yr). The contain: -CO 2 vesicles in various quantities (3-220 ppm C) with delta 13 C between -4 and -9per mille relative to PDB, in the range of carbonatites and diamonds. - Carbonate carbon (3-100 ppm C) with delta 13 C between -2.6 and -20.0per mille relative to PDB. - Dissolved carbon at a concentration of 170+-10 ppm under 250 bar pressure with delta 13 C from -9 to -21per mille relative to PDB. This dissolved carbon, not contained in large CO 2 vesicles, corresponds to a variety of chemical forms among which part of the above carbonates, microscopic CO 2 bubbles and graphite. The lightest portions of this dissolved carbon are extracted at low temperatures (400-600 0 C) whereas the CO 2 from the vesicles is extracted near fusion temperature. These features can be explained by outgassing processes in two steps from the source region of the magma: (1) equilibrium outgassing before the second percolation threshold, where micron size bubbles are continuously reequilibrated with the magma; (2) distillation after the second percolation threshold when larger bubbles travel faster than magma concentrations to the surface. The second step may begin at different depths apparently related to the spreading rate, shallower for fast-spreading ridges than for slow-spreading ridges. (orig./WL)

  7. Intact tropical forests, new evidence they uptake carbon actively

    Directory of Open Access Journals (Sweden)

    2009-03-01

    Full Text Available According to a paper recently published on Nature, tropical forests play as active carbon sink, absorbing 1.3·109 tons of carbon per year on a global scale. Functional interpretation is not clear yet, but a point is quite easy to realize: tropical forests accumulate and contain more carbon than any other vegetation cover and, if their disruption goes on at current rates, these ecosystems could revert to be a “carbon bomb”, releasing huge amount of CO2 to the atmosphere.

  8. Deep carbon export from a Southern Ocean iron-fertilized diatom bloom

    Digital Repository Service at National Institute of Oceanography (India)

    Smetacek, V.; Klaas, C.; Strass, V.H.; Assmy, P.; Montresor, M.; Cisewski, B.; Savoye, N.; Webb, A.; d’Ovidio, F.; Arrieta, J.M.; Bathmann, U.; Bellerby, R.; Berg, G.M.; Croot, P.; Gonzalez, S.; Henjes, J.; Herndl, G.J.; Hoffmann, L.J.; Leach, H.; Losch, M.; Mills, M.M.; Neill, C.; Peeken, I.; Rottgers, R.; Sachs, O.; Sauter, E.; Schmidt, M.M.; Schwarz, J.; Terbruggen, A.; Wolf-Gladrow, D.

    Fertilization of the ocean by adding iron compounds has induced diatom-dominated phytoplankton blooms accompanied by considerable carbon dioxide drawdown in the ocean surface layer. However, because the fate of bloom biomass could not be adequately...

  9. Intercomparison of Ocean Color Algorithms for Picophytoplankton Carbon in the Ocean

    Directory of Open Access Journals (Sweden)

    Víctor Martínez-Vicente

    2017-12-01

    Full Text Available The differences among phytoplankton carbon (Cphy predictions from six ocean color algorithms are investigated by comparison with in situ estimates of phytoplankton carbon. The common satellite data used as input for the algorithms is the Ocean Color Climate Change Initiative merged product. The matching in situ data are derived from flow cytometric cell counts and per-cell carbon estimates for different types of pico-phytoplankton. This combination of satellite and in situ data provides a relatively large matching dataset (N > 500, which is independent from most of the algorithms tested and spans almost two orders of magnitude in Cphy. Results show that not a single algorithm outperforms any of the other when using all matching data. Concentrating on the oligotrophic regions (Chlorophyll-a concentration, B, less than 0.15 mg Chl m−3, where flow cytometric analysis captures most of the phytoplankton biomass, reveals significant differences in algorithm performance. The bias ranges from −35 to +150% and unbiased root mean squared difference from 5 to 10 mg C m−3 among algorithms, with chlorophyll-based algorithms performing better than the rest. The backscattering-based algorithms produce different results at the clearest waters and these differences are discussed in terms of the different algorithms used for optical particle backscattering coefficient (bbp retrieval.

  10. Regional variations in the fluxes of foraminifera carbonate, coccolithophorid carbonate and biogenic opal in the northern Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Ramaswamy, V.; Gaye, B.

    Mass fluxes of diatom opal, planktonic foraminifera carbonate and coccolithophorid carbonate were measured with time-series sediment traps at six sites in the Arabian Sea, Bay of Bengal and Equatorial Indian Ocean (EIOT). The above fluxes were...

  11. Non-riverine pathways of terrigenous carbon to the ocean

    Science.gov (United States)

    Dittmar, T.

    2007-12-01

    The extent and nature of non-riverine fluxes of carbon from land to ocean are poorly understood. Tidal pumping from highly productive coastal environments, atmospheric deposition and submarine groundwater discharge can be significant transport mechanisms for carbon to the ocean. Evidence is mounting that tidally-induced porewater fluxes ("outwelling") of dissolved organic matter (DOM) from mangroves and salt marshes alone may be similar in magnitude as the global riverine flux of DOM. Tidal pumping of dissolved inorganic carbon (DIC) might exceed organic carbon fluxes by far, but the existing knowledge on DIC outwelling is too scarce for a first global estimate. Results from two case studies on the biogeochemistry of DOM outwelling are presented, from the mangroves in Northern Brazil and the salt marshes in the Northern Gulf of Mexico. Ongoing research in the Northern Gulf of Mexico indicates that outwelling and groundwater inputs probably exceed riverine DOM fluxes in this region. Similar observations were made in Northern Brazil. There, the fate of mangrove-derived DOM could be traced from its source in the mangrove sediments to the outer North Brazil shelf by using a combination of isotopic and molecular approaches. Reversed-phase liquid chromatography / mass spectrometry (LC/MS) provided a multifaceted array of information that mirrors the molecular complexity of DOM. Statistical analyses on these data revealed significant differences between mangrove and open-ocean DOM which successively disappeared by irradiating the samples with natural sunlight. Nuclear magnetic resonance analyses yielded concurrent results. Ultrahigh-resolution Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS) is the only technique capable of resolving and identifying individual elemental compositions in these complex mixtures. We applied this technique for characterizing mangrove-derived DOM and to assess the molecular changes that occur in the initial stages of

  12. Large uncertainty in carbon uptake potential of land-based climate-change mitigation efforts.

    Science.gov (United States)

    Krause, Andreas; Pugh, Thomas A M; Bayer, Anita D; Li, Wei; Leung, Felix; Bondeau, Alberte; Doelman, Jonathan C; Humpenöder, Florian; Anthoni, Peter; Bodirsky, Benjamin L; Ciais, Philippe; Müller, Christoph; Murray-Tortarolo, Guillermo; Olin, Stefan; Popp, Alexander; Sitch, Stephen; Stehfest, Elke; Arneth, Almut

    2018-07-01

    Most climate mitigation scenarios involve negative emissions, especially those that aim to limit global temperature increase to 2°C or less. However, the carbon uptake potential in land-based climate change mitigation efforts is highly uncertain. Here, we address this uncertainty by using two land-based mitigation scenarios from two land-use models (IMAGE and MAgPIE) as input to four dynamic global vegetation models (DGVMs; LPJ-GUESS, ORCHIDEE, JULES, LPJmL). Each of the four combinations of land-use models and mitigation scenarios aimed for a cumulative carbon uptake of ~130 GtC by the end of the century, achieved either via the cultivation of bioenergy crops combined with carbon capture and storage (BECCS) or avoided deforestation and afforestation (ADAFF). Results suggest large uncertainty in simulated future land demand and carbon uptake rates, depending on the assumptions related to land use and land management in the models. Total cumulative carbon uptake in the DGVMs is highly variable across mitigation scenarios, ranging between 19 and 130 GtC by year 2099. Only one out of the 16 combinations of mitigation scenarios and DGVMs achieves an equivalent or higher carbon uptake than achieved in the land-use models. The large differences in carbon uptake between the DGVMs and their discrepancy against the carbon uptake in IMAGE and MAgPIE are mainly due to different model assumptions regarding bioenergy crop yields and due to the simulation of soil carbon response to land-use change. Differences between land-use models and DGVMs regarding forest biomass and the rate of forest regrowth also have an impact, albeit smaller, on the results. Given the low confidence in simulated carbon uptake for a given land-based mitigation scenario, and that negative emissions simulated by the DGVMs are typically lower than assumed in scenarios consistent with the 2°C target, relying on negative emissions to mitigate climate change is a highly uncertain strategy. © 2018 John

  13. Late quaternary fluctuations in carbonate and carbonate ion content in the northern Indian ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Naik, S.S.

    -normalized carbonate ion (CO3=*) range from 90 to 125µmol kg-1 in the tropical region of the world oceans with a weight los of 0.3 ± 0.05µg mol -1kg-1 (Broecker and Clark, 201d). Botm water CO3=* concentration bathing the core tops are in the range of 88 to 13 μmolkg-1...

  14. Combining multiple ecosystem productivity measurements to constrain carbon uptake estimates in semiarid grasslands and shrublands

    Science.gov (United States)

    Maurer, G. E.; Krofcheck, D. J.; Collins, S. L.; Litvak, M. E.

    2016-12-01

    Recent observational and modeling studies have indicated that semiarid ecosystems are more dynamic contributors to the global carbon budget than once thought. Semiarid carbon fluxes, however, are generally small, with high interannual and spatial variability, which suggests that validating their global significance may depend on examining multiple productivity measures and their associated uncertainties and inconsistencies. We examined ecosystem productivity from eddy covariance (NEE), harvest (NPP), and terrestrial biome models (NEPm) at two very similar grassland sites and one creosote shrubland site in the Sevilleta National Wildlife Refuge of central New Mexico, USA. Our goal was to assess site and methodological correspondence in annual carbon uptake, patterns of interannual variability, and measurement uncertainty. One grassland site was a perennial carbon source losing 30 g C m-2 per year on average, while the other two sites were carbon sources or sinks depending on the year, with average net uptake of 5 and 25 g C m-2 per year at the grassland and shrubland site, respectively. Uncertainty values for cumulative annual NEE overlapped between the three sites in most years. When combined, aboveground and belowground annual NPP measurements were 15% higher than annual NEE values and did not confirm a loss of carbon at any site in any year. Despite differences in mean site carbon balance, year-to-year changes in cumulative annual NEE and NPP were similar at all sites with years 2010 and 2013 being favorable for carbon uptake and 2011 and 2012 being unfavorable at all sites. Modeled NEPm data for a number of nearby grid cells reproduced only a fraction of the observed range in carbon uptake and its interannual variability. These three sites are highly similar in location and climate and multiple carbon flux measurements confirm the high interannual variability in carbon flux. The exact magnitude of these fluxes, however, remains difficult to discern.

  15. Transforming Ocean Observations of the Carbon Budget, Acidification, Hypoxia, Nutrients, and Biological Productivity: a Global Array of Biogeochemical Argo Floats

    Science.gov (United States)

    Talley, L. D.; Johnson, K. S.; Claustre, H.; Boss, E.; Emerson, S. R.; Westberry, T. K.; Sarmiento, J. L.; Mazloff, M. R.; Riser, S.; Russell, J. L.

    2017-12-01

    Our ability to detect changes in biogeochemical (BGC) processes in the ocean that may be driven by increasing atmospheric CO2, as well as by natural climate variability, is greatly hindered by undersampling in vast areas of the open ocean. Argo is a major international program that measures ocean heat content and salinity with about 4000 floats distributed throughout the ocean, profiling to 2000 m every 10 days. Extending this approach to a global BGC-Argo float array, using recent, proven sensor technology, and in close synergy with satellite systems, will drive a transformative shift in observing and predicting the effects of climate change on ocean metabolism, carbon uptake, acidification, deoxygenation, and living marine resource management. BGC-Argo will add sensors for pH, oxygen, nitrate, chlorophyll, suspended particles, and downwelling irradiance, with sufficient accuracy for climate studies. Observing System Simulation Experiments (OSSEs) using BGC models indicate that 1000 BGC floats would provide sufficient coverage, hence equipping 1/4 of the Argo array. BGC-Argo (http://biogeochemical-argo.org) will enhance current sustained observational programs such as Argo, GO-SHIP, and long-term ocean time series. BGC-Argo will benefit from deployments on GO-SHIP vessels, which provide sensor verification. Empirically derived algorithms that relate the observed BGC float parameters to the carbon system parameters will provide global information on seasonal ocean-atmosphere carbon exchange. BGC Argo measurements could be paired with other emerging technology, such as pCO2 measurements from ships of opportunity and wave gliders, to extend and validate exchange estimates. BGC-Argo prototype programs already show the potential of a global observing system that can measure seasonal to decadal variability. Various countries have developed regional BGC arrays: Southern Ocean (SOCCOM), North Atlantic Subpolar Gyre (remOcean), Mediterranean (NAOS), the Kuroshio (INBOX

  16. Physiological conditions and uptake of inorganic carbon-14 by plant roots

    International Nuclear Information System (INIS)

    Amiro, B.D.; Ewing, L.L.

    1992-01-01

    The uptake of inorganic 14 C by bean plant roots was measured. The plants were grown in a nutrient solution culture at pH 6 and a NaH 14 CO 3 tracer was added to the growth medium. Photosynthesis and transpiration were varied by exposing the aerial portions of the plants to different atmospheric CO 2 concentrations, humidities and light levels in a cuvette system. Leaf concentrations of 14 C were measured at the end of the experiments using liquid scintillation counting. Plant uptake of 14 C via the roots was independent of the photosynthetic rate and, in most cases, could be predicted by knowing the transpiration rate and the nutrient solution concentration. However, when a less efficient root-medium aeration system was used, 14 C uptake was greater than that predicted using transpiration, a phenomenon observed by other researchers. This contrasted to results of another experiment where the measured uptake of iodine was much slower than that predicted using transpiration. Knowledge of transpiration rates is useful in predicting inorganic carbon uptake via the roots and in estimating 14 C transport from contaminated soils to biota. Also, the independence of the uptake from photosynthesis and ambient CO 2 concentrations suggests that future increases in atmospheric CO 2 concentrations may not have a direct effect on root uptake of soil carbon. (author)

  17. Sensitivity of the regional ocean acidification and carbonate system in Puget Sound to ocean and freshwater inputs

    Directory of Open Access Journals (Sweden)

    Laura Bianucci

    2018-03-01

    Full Text Available While ocean acidification was first investigated as a global phenomenon, coastal acidification has received significant attention in recent years, as its impacts have been felt by different socio-economic sectors (e.g., high mortality of shellfish larvae in aquaculture farms. As a region that connects land and ocean, the Salish Sea (consisting of Puget Sound and the Straits of Juan de Fuca and Georgia receives inputs from many different sources (rivers, wastewater treatment plants, industrial waste treatment facilities, etc., making these coastal waters vulnerable to acidification. Moreover, the lowering of pH in the Northeast Pacific Ocean also affects the Salish Sea, as more acidic waters get transported into the bottom waters of the straits and estuaries. Here, we use a numerical ocean model of the Salish Sea to improve our understanding of the carbonate system in Puget Sound; in particular, we studied the sensitivity of carbonate variables (e.g., dissolved inorganic carbon, total alkalinity, pH, saturation state of aragonite to ocean and freshwater inputs. The model is an updated version of our FVCOM-ICM framework, with new carbonate-system and sediment modules. Sensitivity experiments altering concentrations at the open boundaries and freshwater sources indicate that not only ocean conditions entering the Strait of Juan de Fuca, but also the dilution of carbonate variables by freshwater sources, are key drivers of the carbonate system in Puget Sound.

  18. Somewhere beyond the sea? The oceanic - carbon dioxide - reactions

    Science.gov (United States)

    Meisinger, Philipp; Wittlich, Christian

    2014-05-01

    In correlation to climate change and CO2 emission different campaigns highlight the importance of forests and trees to regulate the concentration of carbon dioxide in the earths' atmosphere. Seeing millions of square miles of rainforest cut down every day, this is truly a valid point. Nevertheless, we often tend to forget what scientists like Spokes try to raise awareness for: The oceans - and foremost deep sea sections - resemble the second biggest deposit of carbon dioxide. Here carbon is mainly found in form of carbonate and hydrogen carbonate. The carbonates are needed by corals and other sea organisms to maintain their skeletal structure and thereby to remain vital. To raise awareness for the protection of this fragile ecosystem in schools is part of our approach. Awareness is achieved best through understanding. Therefore, our approach is a hands-on activity that aims at showing students how the carbon dioxide absorption changes in relation to the water temperature - in times of global warming a truly sensitive topic. The students use standard syringes filled with water (25 ml) at different temperatures (i.e. 10°C, 20°C, 40°C). Through a connector students inject carbon dioxide (25ml) into the different samples. After a fixed period of time, students can read of the remaining amount of carbon dioxide in relation to the given water temperature. Just as with every scientific project, students need to closely monitor their experiments and alter their setups (e.g. water temperature or acidity) according to their initial planning. A digital template (Excel-based) supports the analysis of students' experiments. Overview: What: hands-on, minds -on activity using standard syringes to exemplify carbon dioxide absorption in relation to the water temperature (Le Chatelier's principle) For whom: adjustable from German form 11-13 (age: 16-19 years) Time: depending on the prior knowledge 45-60 min. Sources (extract): Spokes, L.: Wie Ozeane CO2 aufnehmen. Environmental

  19. Effect of ocean acidification on the benthic foraminifera Ammonia sp. is caused by a decrease in carbonate ion concentration

    Directory of Open Access Journals (Sweden)

    N. Keul

    2013-10-01

    Full Text Available About 30% of the anthropogenically released CO2 is taken up by the oceans; such uptake causes surface ocean pH to decrease and is commonly referred to as ocean acidification (OA. Foraminifera are one of the most abundant groups of marine calcifiers, estimated to precipitate ca. 50 % of biogenic calcium carbonate in the open oceans. We have compiled the state of the art literature on OA effects on foraminifera, because the majority of OA research on this group was published within the last three years. Disparate responses of this important group of marine calcifiers to OA were reported, highlighting the importance of a process-based understanding of OA effects on foraminifera. We cultured the benthic foraminifer Ammonia sp. under a range of carbonate chemistry manipulation treatments to identify the parameter of the carbonate system causing the observed effects. This parameter identification is the first step towards a process-based understanding. We argue that [CO32−] is the parameter affecting foraminiferal size-normalized weights (SNWs and growth rates. Based on the presented data, we can confirm the strong potential of Ammonia sp. foraminiferal SNW as a [CO32−] proxy.

  20. The time aspect of bioenergy. Climate impacts of bioenergy due to differences in carbon uptake rates

    Energy Technology Data Exchange (ETDEWEB)

    Zetterberg, Lars [IVL Swedish Environmental Research Institute, Stockholm (Sweden); Chen, Deliang [Dept. of Earth Sciences, Univ. of Gothenburg, Gothenburg (Sweden)

    2011-07-01

    This paper investigates the climate impacts from bioenergy due to how they influence carbon stocks over time and more specifically how fast combustion related carbon emissions are compensated by uptake of atmospheric carbon. A set of fuel types representing different uptake rates are investigated, namely willow, branches and tops, stumps and coal. Net emissions are defined as emissions from utilizing the fuel minus emissions from a reference case of no utilisation. In the case of forest residues, the compensating 'uptake' is avoided emissions from the reference case of leaving the residues to decompose on the ground. Climate impacts are estimated using the measures radiative forcing and global average surface temperature, which have been calculated by an energy balance climate model. We conclude that there is a climate impact from using bioenergy due to how fast the emission pulse is compensated by uptake of atmospheric carbon (or avoided emissions). Biofuels with slower uptake rates have a stronger climate impact than fuels with a faster uptake rate, assuming all other parameters equal. The time perspective over which the analysis is done is crucial for the climate impact of biofuels. If only biogenic fluxes are considered, our results show that over a 100 year perspective branches and tops are better for climate mitigation than stumps which in turn are better than coal. Over a 20 year time perspective this conclusion holds, but the differences between these fuels are relatively smaller. Establishing willow on earlier crop land may reduce atmospheric carbon, provided new land is available. However, these results are inconclusive since we haven't considered the effects, if needed, of producing the traditional agricultural crops elsewhere. The analysis is not a life cycle assessment of different fuels and does therefore not consider the use of fossil fuels for logging, transportation and refining, other greenhouse gases than carbon or energy

  1. The Southern Ocean's role in carbon exchange during the last deglaciation.

    Science.gov (United States)

    Burke, Andrea; Robinson, Laura F

    2012-02-03

    Changes in the upwelling and degassing of carbon from the Southern Ocean form one of the leading hypotheses for the cause of glacial-interglacial changes in atmospheric carbon dioxide. We present a 25,000-year-long Southern Ocean radiocarbon record reconstructed from deep-sea corals, which shows radiocarbon-depleted waters during the glacial period and through the early deglaciation. This depletion and associated deep stratification disappeared by ~14.6 ka (thousand years ago), consistent with the transfer of carbon from the deep ocean to the surface ocean and atmosphere via a Southern Ocean ventilation event. Given this evidence for carbon exchange in the Southern Ocean, we show that existing deep-ocean radiocarbon records from the glacial period are sufficiently depleted to explain the ~190 per mil drop in atmospheric radiocarbon between ~17 and 14.5 ka.

  2. Carbon dioxide, climate and the deep ocean circulation: Carbon chemistry model

    International Nuclear Information System (INIS)

    Menawat, A.S.

    1992-01-01

    The objective of this study was to investigate the role of oceanic carbon chemistry in modulating the atmospheric levels of CO 2 . It is well known that the oceans are the primary sink of the excess carbon pumped into the atmosphere since the beginning of the industrial period. The suspended particulate and the dissolved organic matters in the deep ocean play important roles as carriers of carbon and other elements critical to the fate of CO 2 . In addition, the suspended particulate matter provides sites for oxidation-reduction reactions and microbial activities. The problem is of an intricate system with complex chemical, physical and biological processes. This report describes a methodology to describe the interconversions of different forms of the organic and inorganic nutrients, that may be incorporated in the ocean circulation models. Our approach includes the driving force behind the transfers in addition to balancing the elements. Such thermodynamic considerations of describing the imbalance in the chemical potentials is a new and unique feature of our approach

  3. EPOCA/EUR-OCEANS data compilation on the biological and biogeochemical responses to ocean acidification

    OpenAIRE

    Nisumaa Anne-Marin; Pesant Stephane; Bellerby Richard G J; Delille Bruno; Middelburg Jack J; Orr James C; Riebesell Ulf; Tyrrell Toby; Wolf-Gladrow Dieter A; Gattuso Jean-Pierre

    2010-01-01

    The uptake of anthropogenic CO2 by the oceans has led to a rise in the oceanic partial pressure of CO2, and to a decrease in pH and carbonate ion concentration. This modification of the marine carbonate system is referred to as ocean acidification. Numerous papers report the effects of ocean acidification on marine organisms and communities but few have provided details concerning full carbonate chemistry and complementary observations. Additional...

  4. Can frequent precipitation moderate the impact of drought on peatmoss carbon uptake in northern peatlands?

    Science.gov (United States)

    Nijp, Jelmer J; Limpens, Juul; Metselaar, Klaas; van der Zee, Sjoerd E A T M; Berendse, Frank; Robroek, Bjorn J M

    2014-07-01

    Northern peatlands represent a large global carbon store that can potentially be destabilized by summer water table drawdown. Precipitation can moderate the negative impacts of water table drawdown by rewetting peatmoss (Sphagnum spp.), the ecosystem's key species. Yet, the frequency of such rewetting required for it to be effective remains unknown. We experimentally assessed the importance of precipitation frequency for Sphagnum water supply and carbon uptake during a stepwise decrease in water tables in a growth chamber. CO2 exchange and the water balance were measured for intact cores of three peatmoss species (Sphagnum majus, Sphagnum balticum and Sphagnum fuscum) representative of three hydrologically distinct peatland microhabitats (hollow, lawn and hummock) and expected to differ in their water table-precipitation relationships. Precipitation contributed significantly to peatmoss water supply when the water table was deep, demonstrating the importance of precipitation during drought. The ability to exploit transient resources was species-specific; S. fuscum carbon uptake increased linearly with precipitation frequency for deep water tables, whereas carbon uptake by S. balticum and S. majus was depressed at intermediate precipitation frequencies. Our results highlight an important role for precipitation in carbon uptake by peatmosses. Yet, the potential to moderate the impact of drought is species-specific and dependent on the temporal distribution of precipitation. © 2014 The Authors. New Phytologist © 2014 New Phytologist Trust.

  5. Impact of idealized future stratospheric aerosol injection on the large-scale ocean and land carbon cycles

    Science.gov (United States)

    Tjiputra, J. F.; Grini, A.; Lee, H.

    2016-01-01

    Using an Earth system model, we simulate stratospheric aerosol injection (SAI) on top of the Representative Concentration Pathways 8.5 future scenario. Our idealized method prescribes aerosol concentration, linearly increasing from 2020 to 2100, and thereafter remaining constant until 2200. In the aggressive scenario, the model projects a cooling trend toward 2100 despite warming that persists in the high latitudes. Following SAI termination in 2100, a rapid global warming of 0.35 K yr-1 is simulated in the subsequent 10 years, and the global mean temperature returns to levels close to the reference state, though roughly 0.5 K cooler. In contrast to earlier findings, we show a weak response in the terrestrial carbon sink during SAI implementation in the 21st century, which we attribute to nitrogen limitation. The SAI increases the land carbon uptake in the temperate forest-, grassland-, and shrub-dominated regions. The resultant lower temperatures lead to a reduction in the heterotrophic respiration rate and increase soil carbon retention. Changes in precipitation patterns are key drivers for variability in vegetation carbon. Upon SAI termination, the level of vegetation carbon storage returns to the reference case, whereas the soil carbon remains high. The ocean absorbs nearly 10% more carbon in the geoengineered simulation than in the reference simulation, leading to a ˜15 ppm lower atmospheric CO2 concentration in 2100. The largest enhancement in uptake occurs in the North Atlantic. In both hemispheres' polar regions, SAI delays the sea ice melting and, consequently, export production remains low. In the deep water of North Atlantic, SAI-induced circulation changes accelerate the ocean acidification rate and broaden the affected area.

  6. The Global Influence of Cloud Optical Thickness on Terrestrial Carbon Uptake

    Science.gov (United States)

    Zhu, P.; Cheng, S. J.; Keppel-Aleks, G.; Butterfield, Z.; Steiner, A. L.

    2016-12-01

    Clouds play a critical role in regulating Earth's climate. One important way is by changing the type and intensity of solar radiation reaching the Earth's surface, which impacts plant photosynthesis. Specifically, the presence of clouds modifies photosynthesis rates by influencing the amount of diffuse radiation as well as the spectral distribution of solar radiation. Satellite-derived cloud optical thickness (COT) may provide the observational constraint necessary to assess the role of clouds on ecosystems and terrestrial carbon uptake across the globe. Previous studies using ground-based observations at individual sites suggest that below a COT of 7, there is a greater increase in light use efficiency than at higher COT values, providing evidence for higher carbon uptake rates than expected given the reduction in radiation by clouds. However, the strength of the COT-terrestrial carbon uptake correlation across the globe remains unknown. In this study, we investigate the influence of COT on terrestrial carbon uptake on a global scale, which may provide insights into cloud conditions favorable for plant photosynthesis and improve our estimates of the land carbon sink. Global satellite-derived MODIS data show that tropical and subtropical regions tend to have COT values around or below the threshold during growing seasons. We find weak correlations between COT and GPP with Fluxnet MTE global GPP data, which may be due to the uncertainty of upscaling GPP from individual site measurements. Analysis with solar-induced fluorescence (SIF) as a proxy for GPP is also evaluated. Overall, this work constructs a global picture of the role of COT on terrestrial carbon uptake, including its temporal and spatial variations.

  7. Ocean acidification over the next three centuries using a simple global climate carbon-cycle model: projections and sensitivities

    Energy Technology Data Exchange (ETDEWEB)

    Hartin, Corinne A.; Bond-Lamberty, Benjamin; Patel, Pralit; Mundra, Anupriya

    2016-08-01

    Continued oceanic uptake of anthropogenic CO2 is projected to significantly alter the chemistry of the upper oceans over the next three centuries, with potentially serious consequences for marine ecosystems. Relatively few models have the capability to make projections of ocean acidification, limiting our ability to assess the impacts and probabilities of ocean changes. In this study we examine the ability of Hector v1.1, a reduced-form global model, to project changes in the upper ocean carbonate system over the next three centuries, and quantify the model's sensitivity to parametric inputs. Hector is run under prescribed emission pathways from the Representative Concentration Pathways (RCPs) and compared to both observations and a suite of Coupled Model Intercomparison (CMIP5) model outputs. Current observations confirm that ocean acidification is already taking place, and CMIP5 models project significant changes occurring to 2300. Hector is consistent with the observational record within both the high- (> 55°) and low-latitude oceans (< 55°). The model projects low-latitude surface ocean pH to decrease from preindustrial levels of 8.17 to 7.77 in 2100, and to 7.50 in 2300; aragonite saturation levels (ΩAr) decrease from 4.1 units to 2.2 in 2100 and 1.4 in 2300 under RCP 8.5. These magnitudes and trends of ocean acidification within Hector are largely consistent with the CMIP5 model outputs, although we identify some small biases within Hector's carbonate system. Of the parameters tested, changes in [H+] are most sensitive to parameters that directly affect atmospheric CO2 concentrations – Q10 (terrestrial respiration temperature response) as well as changes in ocean circulation, while changes in ΩAr saturation levels are sensitive to changes in ocean salinity and Q10. We conclude that Hector is a robust tool well suited for rapid ocean acidification

  8. Using satellite-derived optical thickness to assess the influence of clouds on terrestrial carbon uptake

    Science.gov (United States)

    S.J. Cheng; A.L. Steiner; D.Y. Hollinger; G. Bohrer; K.J. Nadelhoffer

    2016-01-01

    Clouds scatter direct solar radiation, generating diffuse radiation and altering the ratio of direct to diffuse light. If diffuse light increases plant canopy CO2 uptake, clouds may indirectly influence climate by altering the terrestrial carbon cycle. However, past research primarily uses proxies or qualitative categories of clouds to connect...

  9. Changes in ocean circulation and carbon storage are decoupled from air-sea CO2 fluxes

    Science.gov (United States)

    Marinov, I.; Gnanadesikan, A.

    2011-02-01

    The spatial distribution of the air-sea flux of carbon dioxide is a poor indicator of the underlying ocean circulation and of ocean carbon storage. The weak dependence on circulation arises because mixing-driven changes in solubility-driven and biologically-driven air-sea fluxes largely cancel out. This cancellation occurs because mixing driven increases in the poleward residual mean circulation result in more transport of both remineralized nutrients and heat from low to high latitudes. By contrast, increasing vertical mixing decreases the storage associated with both the biological and solubility pumps, as it decreases remineralized carbon storage in the deep ocean and warms the ocean as a whole.

  10. USGS Arctic Ocean carbon cruise 2010: field activity H-03-10-AR to collect carbon data in the Arctic Ocean, August - September 2010

    Science.gov (United States)

    Robbins, Lisa L.; Yates, Kimberly K.; Gove, Matthew D.; Knorr, Paul O.; Wynn, Jonathan; Byrne, Robert H.; Liu, Xuewu

    2013-01-01

    Carbon dioxide (CO2) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form carbonic acid, a weak, naturally occurring acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

  11. USGS Arctic Ocean carbon cruise 2011: field activity H-01-11-AR to collect carbon data in the Arctic Ocean, August - September 2011

    Science.gov (United States)

    Robbins, Lisa L.; Yates, Kimberly K.; Knorr, Paul O.; Wynn, Jonathan; Lisle, John; Buczkowski, Brian J.; Moore, Barbara; Mayer, Larry; Armstrong, Andrew; Byrne, Robert H.; Liu, Xuewu

    2013-01-01

    Carbon dioxide (CO2) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form a weak, naturally occurring acid called carbonic acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

  12. Carbon dioxide in northern high latitude oceans: Anthropogenic increase and air-sea flux variability

    International Nuclear Information System (INIS)

    Omar, Abdirahman M.

    2003-01-01

    The aim of this thesis is to further our knowledge of carbon dioxide in the northern high latitude oceans (northern North Atlantic, Barents Sea, and Arctic Ocean) by studying the anthropogenic change in the oceanic CO2, the inter-annual variability of the air-sea CO2 flux, and the relationship between this variability and changes in other oceanic processes. An introductory chapter and four papers are presented. Descriptions of the seawater carbonate system parameters, air-sea exchange of CO2, and related processes are given in the introduction chapter. The anthropogenic increase in partial pressure of CO2 (pCO2) in the surface water of the Barents Sea is evaluated in paper I. The effect of alternations of the Barents Sea climate between cold and warm modes on the annual cycles of seawater fugacity and air-sea flux of CO2 is investigated in paper II. Oceanic uptake of atmospheric CO2 associated with the seasonal formation of sea ice in Storfjorden and the implication for the entire Arctic Ocean is studied in paper III. An assessment of the variations of the air-sea flux of CO2 in the northern North Atlantic for 20 winters (1981-2001) is carried out in paper IV. PCO2 in the surface water of the Barents Sea is shown to have increased parallel with the atmospheric pCO2 between 1967 and 2000-2001 (paper I). This was determined by comparing seawater pCO2 from 1967 with that from 2000-2001. The former was estimated from surface seawater temperature (SST) while the latter was computed from data of total dissolved inorganic carbon and alkalinity. A procedure which accounts for the natural variability was applied and the difference between seawater pC02 of 1967 and that of 2000-2001 is attributed to the uptake of excess CO2. In the Atlantic sector of the Barents Sea, the surface seawater fugacity of CO2 (fCO s''w) is shown to be lower than the atmospheric fCO2 throughout the year, implying that the area is an annual sink of atmospheric CO2 (paper II). Additionally, changes

  13. Carbon dioxide in northern high latitude oceans: Anthropogenic increase and air-sea flux variability

    Energy Technology Data Exchange (ETDEWEB)

    Omar, Abdirahman M.

    2003-07-01

    The aim of this thesis is to further our knowledge of carbon dioxide in the northern high latitude oceans (northern North Atlantic, Barents Sea, and Arctic Ocean) by studying the anthropogenic change in the oceanic CO2, the inter-annual variability of the air-sea CO2 flux, and the relationship between this variability and changes in other oceanic processes. An introductory chapter and four papers are presented. Descriptions of the seawater carbonate system parameters, air-sea exchange of CO2, and related processes are given in the introduction chapter. The anthropogenic increase in partial pressure of CO2 (pCO2) in the surface water of the Barents Sea is evaluated in paper I. The effect of alternations of the Barents Sea climate between cold and warm modes on the annual cycles of seawater fugacity and air-sea flux of CO2 is investigated in paper II. Oceanic uptake of atmospheric CO2 associated with the seasonal formation of sea ice in Storfjorden and the implication for the entire Arctic Ocean is studied in paper III. An assessment of the variations of the air-sea flux of CO2 in the northern North Atlantic for 20 winters (1981-2001) is carried out in paper IV. PCO2 in the surface water of the Barents Sea is shown to have increased parallel with the atmospheric pCO2 between 1967 and 2000-2001 (paper I). This was determined by comparing seawater pCO2 from 1967 with that from 2000-2001. The former was estimated from surface seawater temperature (SST) while the latter was computed from data of total dissolved inorganic carbon and alkalinity. A procedure which accounts for the natural variability was applied and the difference between seawater pC02 of 1967 and that of 2000-2001 is attributed to the uptake of excess CO2. In the Atlantic sector of the Barents Sea, the surface seawater fugacity of CO2 (fCO s''w) is shown to be lower than the atmospheric fCO2 throughout the year, implying that the area is an annual sink of atmospheric CO2 (paper II). Additionally

  14. Remote Sensing of Evapotranspiration and Carbon Uptake at Harvard Forest

    Science.gov (United States)

    Min, Qilong; Lin, Bing

    2005-01-01

    A land surface vegetation index, defined as the difference of microwave land surface emissivity at 19 and 37 GHz, was calculated for a heavily forested area in north central Massachusetts. The microwave emissivity difference vegetation index (EDVI) was estimated from satellite SSM/I measurements at the defined wavelengths and used to estimate land surface turbulent fluxes. Narrowband visible and infrared measurements and broadband solar radiation observations were used in the EDVI retrievals and turbulent flux estimations. The EDVI values represent physical properties of crown vegetation such as vegetation water content of crown canopies. The collocated land surface turbulent and radiative fluxes were empirically linked together by the EDVI values. The EDVI values are statistically sensitive to evapotranspiration fractions (EF) with a correlation coefficient (R) greater than 0.79 under all-sky conditions. For clear skies, EDVI estimates exhibit a stronger relationship with EF than normalized difference vegetation index (NDVI). Furthermore, the products of EDVI and input energy (solar and photosynthetically-active radiation) are statistically significantly correlated to evapotranspiration (R=0.95) and CO2 uptake flux (R=0.74), respectively.

  15. Nitrogen uptake by phytoplankton in surface waters of the Indian sector of Southern Ocean during austral summer

    Science.gov (United States)

    Tripathy, S. C.; Patra, Sivaji; Vishnu Vardhan, K.; Sarkar, A.; Mishra, R. K.; Anilkumar, N.

    2018-03-01

    This study reports the nitrogen uptake rate (using 15N tracer) of phytoplankton in surface waters of different frontal zones in the Indian sector of the Southern Ocean (SO) during austral summer of 2013. The investigated area encompasses four major frontal systems, i.e., the subtropical front (STF), subantarctic front (SAF), polar front-1 (PF1) and polar front-2 (PF2). Southward decrease of surface water temperature was observed, whereas surface salinity did not show any significant trend. Nutrient (NO3 - and SiO4 4-) concentrations increased southward from STF to PF; while ammonium (NH4 +), nitrite (NO2 -) and phosphate (PO4 3-) remained comparatively stable. Analysis of nutrient ratios indicated potential N-limited conditions at the STF and SAF but no such scenario was observed for PF. In terms of phytoplankton biomass, PF1 was found to be the most productive followed by SAF, whereas PF2 was the least productive region. Nitrate uptake rate increased with increasing latitude, as no systematic spatial variation was discerned for NH4 + and urea (CO(NH2)2). Linear relationship between nitrate and total N-uptake reveals that the studied area is capable of exporting up to 60% of the total production to the deep ocean if the environmental settings are favorable. Like N-uptake rates the f-ratio also increased towards PF region indicating comparatively higher new production in the PF than in the subtropics. The moderately high average f-ratio (0.53) indicates potentially near equal contributions by new production and regenerated production to the total productivity in the study area. Elevation in N-uptake rates with declining temperature suggests that the SO with its vast quantity of cool water could play an important role in drawing down the atmospheric CO2 through the "solubility pump".

  16. Estimating the carbon budget and maximizing future carbon uptake for a temperate forest region in the U.S.

    Science.gov (United States)

    2012-01-01

    Background Forests of the Midwest U.S. provide numerous ecosystem services. Two of these, carbon sequestration and wood production, are often portrayed as conflicting. Currently, carbon management and biofuel policies are being developed to reduce atmospheric CO2 and national dependence on foreign oil, and increase carbon storage in ecosystems. However, the biological and industrial forest carbon cycles are rarely studied in a whole-system structure. The forest system carbon balance is the difference between the biological (net ecosystem production) and industrial (net emissions from forest industry) forest carbon cycles, but to date this critical whole system analysis is lacking. This study presents a model of the forest system, uses it to compute the carbon balance, and outlines a methodology to maximize future carbon uptake in a managed forest region. Results We used a coupled forest ecosystem process and forest products life cycle inventory model for a regional temperate forest in the Midwestern U.S., and found the net system carbon balance for this 615,000 ha forest was positive (2.29 t C ha-1 yr-1). The industrial carbon budget was typically less than 10% of the biological system annually, and averaged averaged 0.082 t C ha-1 yr-1. Net C uptake over the next 100-years increased by 22% or 0.33 t C ha-1 yr-1 relative to the current harvest rate in the study region under the optized harvest regime. Conclusions The forest’s biological ecosystem current and future carbon uptake capacity is largely determined by forest harvest practices that occurred over a century ago, but we show an optimized harvesting strategy would increase future carbon sequestration, or wood production, by 20-30%, reduce long transportation chain emissions, and maintain many desirable stand structural attributes that are correlated to biodiversity. Our results for this forest region suggest that increasing harvest over the next 100 years increases the strength of

  17. Estimating the carbon budget and maximizing future carbon uptake for a temperate forest region in the U.S.

    Directory of Open Access Journals (Sweden)

    Peckham Scott D

    2012-06-01

    Full Text Available Abstract Background Forests of the Midwest U.S. provide numerous ecosystem services. Two of these, carbon sequestration and wood production, are often portrayed as conflicting. Currently, carbon management and biofuel policies are being developed to reduce atmospheric CO2 and national dependence on foreign oil, and increase carbon storage in ecosystems. However, the biological and industrial forest carbon cycles are rarely studied in a whole-system structure. The forest system carbon balance is the difference between the biological (net ecosystem production and industrial (net emissions from forest industry forest carbon cycles, but to date this critical whole system analysis is lacking. This study presents a model of the forest system, uses it to compute the carbon balance, and outlines a methodology to maximize future carbon uptake in a managed forest region. Results We used a coupled forest ecosystem process and forest products life cycle inventory model for a regional temperate forest in the Midwestern U.S., and found the net system carbon balance for this 615,000 ha forest was positive (2.29 t C ha-1 yr-1. The industrial carbon budget was typically less than 10% of the biological system annually, and averaged averaged 0.082 t C ha-1 yr-1. Net C uptake over the next 100-years increased by 22% or 0.33 t C ha-1 yr-1 relative to the current harvest rate in the study region under the optized harvest regime. Conclusions The forest’s biological ecosystem current and future carbon uptake capacity is largely determined by forest harvest practices that occurred over a century ago, but we show an optimized harvesting strategy would increase future carbon sequestration, or wood production, by 20-30%, reduce long transportation chain emissions, and maintain many desirable stand structural attributes that are correlated to biodiversity. Our results for this forest region suggest that increasing harvest over the next 100

  18. Uncertainty in the global oceanic CO2 uptake induced by wind forcing: quantification and spatial analysis

    Directory of Open Access Journals (Sweden)

    A. Roobaert

    2018-03-01

    Full Text Available The calculation of the air–water CO2 exchange (FCO2 in the ocean not only depends on the gradient in CO2 partial pressure at the air–water interface but also on the parameterization of the gas exchange transfer velocity (k and the choice of wind product. Here, we present regional and global-scale quantifications of the uncertainty in FCO2 induced by several widely used k formulations and four wind speed data products (CCMP, ERA, NCEP1 and NCEP2. The analysis is performed at a 1°  ×  1° resolution using the sea surface pCO2 climatology generated by Landschützer et al. (2015a for the 1991–2011 period, while the regional assessment relies on the segmentation proposed by the Regional Carbon Cycle Assessment and Processes (RECCAP project. First, we use k formulations derived from the global 14C inventory relying on a quadratic relationship between k and wind speed (k = c ⋅ U102; Sweeney et al., 2007; Takahashi et al., 2009; Wanninkhof, 2014, where c is a calibration coefficient and U10 is the wind speed measured 10 m above the surface. Our results show that the range of global FCO2, calculated with these k relationships, diverge by 12 % when using CCMP, ERA or NCEP1. Due to differences in the regional wind patterns, regional discrepancies in FCO2 are more pronounced than global. These global and regional differences significantly increase when using NCEP2 or other k formulations which include earlier relationships (i.e., Wanninkhof, 1992; Wanninkhof et al., 2009 as well as numerous local and regional parameterizations derived experimentally. To minimize uncertainties associated with the choice of wind product, it is possible to recalculate the coefficient c globally (hereafter called c∗ for a given wind product and its spatio-temporal resolution, in order to match the last evaluation of the global k value. We thus performed these recalculations for each wind product at the resolution and time period of our study

  19. Uncertainty in the global oceanic CO2 uptake induced by wind forcing: quantification and spatial analysis

    Science.gov (United States)

    Roobaert, Alizée; Laruelle, Goulven G.; Landschützer, Peter; Regnier, Pierre

    2018-03-01

    The calculation of the air-water CO2 exchange (FCO2) in the ocean not only depends on the gradient in CO2 partial pressure at the air-water interface but also on the parameterization of the gas exchange transfer velocity (k) and the choice of wind product. Here, we present regional and global-scale quantifications of the uncertainty in FCO2 induced by several widely used k formulations and four wind speed data products (CCMP, ERA, NCEP1 and NCEP2). The analysis is performed at a 1° × 1° resolution using the sea surface pCO2 climatology generated by Landschützer et al. (2015a) for the 1991-2011 period, while the regional assessment relies on the segmentation proposed by the Regional Carbon Cycle Assessment and Processes (RECCAP) project. First, we use k formulations derived from the global 14C inventory relying on a quadratic relationship between k and wind speed (k = c ṡ U102; Sweeney et al., 2007; Takahashi et al., 2009; Wanninkhof, 2014), where c is a calibration coefficient and U10 is the wind speed measured 10 m above the surface. Our results show that the range of global FCO2, calculated with these k relationships, diverge by 12 % when using CCMP, ERA or NCEP1. Due to differences in the regional wind patterns, regional discrepancies in FCO2 are more pronounced than global. These global and regional differences significantly increase when using NCEP2 or other k formulations which include earlier relationships (i.e., Wanninkhof, 1992; Wanninkhof et al., 2009) as well as numerous local and regional parameterizations derived experimentally. To minimize uncertainties associated with the choice of wind product, it is possible to recalculate the coefficient c globally (hereafter called c∗) for a given wind product and its spatio-temporal resolution, in order to match the last evaluation of the global k value. We thus performed these recalculations for each wind product at the resolution and time period of our study but the resulting global FCO2 estimates

  20. Climate change and ocean acidification impacts on lower trophic levels and the export of organic carbon to the deep ocean

    OpenAIRE

    Yool, A.; Popova, E. E.; Coward, A. C.; Bernie, D.; Anderson, T. R.

    2013-01-01

    Most future projections forecast significant and ongoing climate change during the 21st century, but with the severity of impacts dependent on efforts to restrain or reorganise human activity to limit carbon dioxide (CO2) emissions. A major sink for atmospheric CO2, and a key source of biological resources, the World Ocean is widely anticipated to undergo profound physical and – via ocean acidification – chemical changes as direct and indirect results of these emissions. Given strong biophysi...

  1. Restricted Inter-ocean Exchange and Attenuated Biological Export Caused Enhanced Carbonate Preservation in the PETM Ocean

    Science.gov (United States)

    Luo, Y.; Boudreau, B. P.; Dickens, G. R.; Sluijs, A.; Middelburg, J. J.

    2015-12-01

    Carbon dioxide (CO2) release during the Paleocene-Eocene Thermal Maximum (PETM, 55.8 Myr BP) acidified the oceans, causing a decrease in calcium carbonate (CaCO3) preservation. During the subsequent recovery from this acidification, the sediment CaCO3 content came to exceed pre-PETM values, known as over-deepening or over-shooting. Past studies claim to explain these trends, but have failed to reproduce quantitatively the time series of CaCO3 preservation. We employ a simple biogeochemical model to recreate the CaCO3 records preserved at Walvis Ridge of the Atlantic Ocean. Replication of the observed changes, both shallowing and the subsequent over-deepening, requires two conditions not previously considered: (1) limited deep-water exchange between the Indo-Atlantic and Pacific oceans and (2) a ~50% reduction in the export of CaCO3 to the deep sea during acidification. Contrary to past theories that attributed over-deepening to increased riverine alkalinity input, we find that over-deepening is an emergent property, generated at constant riverine input when attenuation of CaCO3 export causes an unbalanced alkalinity input to the deep oceans (alkalinization) and the development of deep super-saturation. Restoration of CaCO3 export, particularly in the super-saturated deep Indo-Atlantic ocean, later in the PETM leads to greater accumulation of carbonates, ergo over-shooting, which returns the ocean to pre-PETM conditions over a time scale greater than 200 kyr. While this feedback between carbonate export and the riverine input has not previously been considered, it appears to constitute an important modification of the classic carbonate compensation concept used to explain oceanic response to acidification.

  2. Ocean Acidification: a review of the current status of research and institutional developments

    NARCIS (Netherlands)

    Beek, van I.J.M.; Dedert, M.

    2012-01-01

    Ocean acidification is defined as the change in ocean chemistry driven by the oceanic uptake of chemical inputs to the atmosphere, including carbon, nitrogen and sulphur compounds. Ocean acidification is also referred to as ‘the other CO2 problem’ of anthropogenic carbon dioxide (CO2) emissions

  3. Estimating carbonate parameters from hydrographic data for the intermediate and deep waters of the Southern Hemisphere oceans

    Science.gov (United States)

    Bostock, H. C.; Mikaloff Fletcher, S. E.; Williams, M. J. M.

    2013-10-01

    Using ocean carbon data from global datasets, we have developed several multiple linear regression (MLR) algorithms to estimate alkalinity and dissolved inorganic carbon (DIC) in the intermediate and deep waters of the Southern Hemisphere (south of 25° S) from only hydrographic data (temperature, salinity and dissolved oxygen). A Monte Carlo experiment was used to identify a potential density (σθ) of 27.5 as an optimal break point between the two regimes with different MLR algorithms. The algorithms provide a good estimate of DIC (R2=0.98) and alkalinity (R2=0.91), and excellent agreement for aragonite and calcite saturation states (R2=0.99). Combining the algorithms with the CSIRO Atlas of Regional Seas (CARS), we have mapped the calcite saturation horizon (CSH) and aragonite saturation horizon (ASH) for the Southern Ocean at a spatial resolution of 0.5°. These maps are more detailed and more consistent with the oceanography than the previously gridded GLODAP data. The high-resolution ASH map reveals a dramatic circumpolar shoaling at the polar front. North of 40° S the CSH is deepest in the Atlantic (~ 4000 m) and shallower in the Pacific Ocean (~ 2750 m), while the CSH sits between 3200 and 3400 m in the Indian Ocean. The uptake of anthropogenic carbon by the ocean will alter the relationships between DIC and hydrographic data in the intermediate and deep waters over time. Thus continued sampling will be required, and the MLR algorithms will need to be adjusted in the future to account for these changes.

  4. Estimating carbonate parameters from hydrographic data for the intermediate and deep waters of the Southern Hemisphere oceans

    Directory of Open Access Journals (Sweden)

    H. C. Bostock

    2013-10-01

    Full Text Available Using ocean carbon data from global datasets, we have developed several multiple linear regression (MLR algorithms to estimate alkalinity and dissolved inorganic carbon (DIC in the intermediate and deep waters of the Southern Hemisphere (south of 25° S from only hydrographic data (temperature, salinity and dissolved oxygen. A Monte Carlo experiment was used to identify a potential density (σθ of 27.5 as an optimal break point between the two regimes with different MLR algorithms. The algorithms provide a good estimate of DIC (R2=0.98 and alkalinity (R2=0.91, and excellent agreement for aragonite and calcite saturation states (R2=0.99. Combining the algorithms with the CSIRO Atlas of Regional Seas (CARS, we have mapped the calcite saturation horizon (CSH and aragonite saturation horizon (ASH for the Southern Ocean at a spatial resolution of 0.5°. These maps are more detailed and more consistent with the oceanography than the previously gridded GLODAP data. The high-resolution ASH map reveals a dramatic circumpolar shoaling at the polar front. North of 40° S the CSH is deepest in the Atlantic (~ 4000 m and shallower in the Pacific Ocean (~ 2750 m, while the CSH sits between 3200 and 3400 m in the Indian Ocean. The uptake of anthropogenic carbon by the ocean will alter the relationships between DIC and hydrographic data in the intermediate and deep waters over time. Thus continued sampling will be required, and the MLR algorithms will need to be adjusted in the future to account for these changes.

  5. [Carbon monoxide tests in a steady state. Uptake and transfer capacity, normal values and lower limits].

    Science.gov (United States)

    Ramonatxo, M; Préfaut, C; Guerrero, H; Moutou, H; Bansard, X; Chardon, G

    1982-01-01

    The aim of this study was to establish data which would best demonstrate the variations of different tests using Carbon Monoxide as a tracer gas (total and partial functional uptake coefficient and transfer capacity) to establish mean values and lower limits of normal of these tests. Multivariate statistical analysis was used; in the first stage a connection was sought between the fractional uptake coefficient (partial and total) to other parameters, comparing subjects and data. In the second stage the comparison was refined by eliminating the least useful data, trying, despite a small loss of material, to reveal the most important connections, linear or otherwise. The fractional uptake coefficients varied according to sex, also the variation of the partial alveolar-expired fractional uptake equivalent (DuACO) was largely a function of respiratory rate and tidal volume. The alveolar-arterial partial fractional uptake equivalent (DuaCO) depended more on respiratory frequency and age. Finally the total fractional uptake coefficient (DuCO) and the transfer capacity corrected per liter of ventilation (TLCO/V) were functions of these parameters. The last stage of this work, after taking account of the statistical observations consistent with the facts of these physiological hypotheses led to a search for a better way of approaching the laws linking the collected data to the fractional uptake coefficient. The lower limits of normal were arbitrarily defined, separating those 5% of subjects deviating most strongly from the mean. As a result, the relationship between the lower limit of normal and the theoretical mean value was 90% for the partial and total fractional uptake coefficient and 70% for the transfer capacity corrected per liter of ventilation.

  6. The influence of the ocean circulation state on ocean carbon storage and CO2 drawdown potential in an Earth system model

    Science.gov (United States)

    Ödalen, Malin; Nycander, Jonas; Oliver, Kevin I. C.; Brodeau, Laurent; Ridgwell, Andy

    2018-03-01

    During the four most recent glacial cycles, atmospheric CO2 during glacial maxima has been lowered by about 90-100 ppm with respect to interglacials. There is widespread consensus that most of this carbon was partitioned in the ocean. It is, however, still debated which processes were dominant in achieving this increased carbon storage. In this paper, we use an Earth system model of intermediate complexity to explore the sensitivity of ocean carbon storage to ocean circulation state. We carry out a set of simulations in which we run the model to pre-industrial equilibrium, but in which we achieve different states of ocean circulation by changing forcing parameters such as wind stress, ocean diffusivity and atmospheric heat diffusivity. As a consequence, the ensemble members also have different ocean carbon reservoirs, global ocean average temperatures, biological pump efficiencies and conditions for air-sea CO2 disequilibrium. We analyse changes in total ocean carbon storage and separate it into contributions by the solubility pump, the biological pump and the CO2 disequilibrium component. We also relate these contributions to differences in the strength of the ocean overturning circulation. Depending on which ocean forcing parameter is tuned, the origin of the change in carbon storage is different. When wind stress or ocean diapycnal diffusivity is changed, the response of the biological pump gives the most important effect on ocean carbon storage, whereas when atmospheric heat diffusivity or ocean isopycnal diffusivity is changed, the solubility pump and the disequilibrium component are also important and sometimes dominant. Despite this complexity, we obtain a negative linear relationship between total ocean carbon and the combined strength of the northern and southern overturning cells. This relationship is robust to different reservoirs dominating the response to different forcing mechanisms. Finally, we conduct a drawdown experiment in which we investigate

  7. The influence of the ocean circulation state on ocean carbon storage and CO2 drawdown potential in an Earth system model

    Directory of Open Access Journals (Sweden)

    M. Ödalen

    2018-03-01

    Full Text Available During the four most recent glacial cycles, atmospheric CO2 during glacial maxima has been lowered by about 90–100 ppm with respect to interglacials. There is widespread consensus that most of this carbon was partitioned in the ocean. It is, however, still debated which processes were dominant in achieving this increased carbon storage. In this paper, we use an Earth system model of intermediate complexity to explore the sensitivity of ocean carbon storage to ocean circulation state. We carry out a set of simulations in which we run the model to pre-industrial equilibrium, but in which we achieve different states of ocean circulation by changing forcing parameters such as wind stress, ocean diffusivity and atmospheric heat diffusivity. As a consequence, the ensemble members also have different ocean carbon reservoirs, global ocean average temperatures, biological pump efficiencies and conditions for air–sea CO2 disequilibrium. We analyse changes in total ocean carbon storage and separate it into contributions by the solubility pump, the biological pump and the CO2 disequilibrium component. We also relate these contributions to differences in the strength of the ocean overturning circulation. Depending on which ocean forcing parameter is tuned, the origin of the change in carbon storage is different. When wind stress or ocean diapycnal diffusivity is changed, the response of the biological pump gives the most important effect on ocean carbon storage, whereas when atmospheric heat diffusivity or ocean isopycnal diffusivity is changed, the solubility pump and the disequilibrium component are also important and sometimes dominant. Despite this complexity, we obtain a negative linear relationship between total ocean carbon and the combined strength of the northern and southern overturning cells. This relationship is robust to different reservoirs dominating the response to different forcing mechanisms. Finally, we conduct a drawdown experiment

  8. Summertime calcium carbonate undersaturation in shelf waters of the western Arctic Ocean – how biological processes exacerbate the impact of ocean acidification

    OpenAIRE

    N. R. Bates; M. I. Orchowska; R. Garley; J. T. Mathis

    2013-01-01

    The Arctic Ocean accounts for only 4% of the global ocean area, but it contributes significantly to the global carbon cycle. Recent observations of seawater CO2-carbonate chemistry in shelf waters of the western Arctic Ocean, primarily in the Chukchi Sea, from 2009 to 2011 indicate that bottom waters are seasonally undersaturated with respect to calcium carbonate (CaCO3) minerals, particularly aragonite. Nearly 40% of sampled bottom waters on the shelf have saturation states...

  9. South African carbon observations: CO2 measurements for land, atmosphere and ocean

    CSIR Research Space (South Africa)

    Feig, Gregor T

    2017-11-01

    Full Text Available , Mudau AE, Monteiro PMS. South African carbon observations: CO2 measurements for land, atmosphere and ocean. S Afr J Sci. 2017;113(11/12), Art. #a0237, 4 pages. http://dx.doi. org/10.17159/sajs.2017/a0237 Carbon dioxide plays a central role in earth... References 1. Houghton RA. Balancing the global carbon budget. Annu Rev Earth Planet Sci. 2007;35:313–347. https://doi.org/10.1146/annurev. earth.35.031306.140057 2. Denman KL. Climate change, ocean processes and ocean iron fertilization. Mar Ecol Prog Ser...

  10. Impact of climatic change on ocean carbon fluxes. Role of the decadal variability

    International Nuclear Information System (INIS)

    Seferian, Roland

    2013-01-01

    Since the industrial revolution, oceans have absorbed roughly one quarter of the anthropogenic emissions of CO 2 , slowing down climate change. The evolution of the ocean carbon sink, paralleled to the anthropogenic CO 2 emissions, is ruled by the CO 2 as well as climate. Influence of atmospheric CO 2 in the recent evolution of the ocean carbon sink is well understood whilst this is not the case for the climate's one. Indeed, some authors claim that the recent variations of the ocean CO 2 sink can be attributed to climate change, whereas some others suggest that these latter are controlled by a decadal variability, which is poorly understood. In this thesis, we address question relative to the role of the decadal variability of the ocean carbon fluxes through the mean of numerical modeling. On one hand, we have demonstrated that ocean carbon fluxes exhibit decadal fluctuations within the high latitudes oceans. These fluctuations displays modes of 10 to 50-year long which account for 20 to 40% of the year-to-year variability. Thanks to Detection and Attribution methods applied to RECCAP project's reconstructions (1960-2005), we have then assessed whether the occurrence of fluctuations at decadal time scale could hamper the detection of the climate contribution to the recent evolution of ocean carbon fluxes. We have shown that the climate contribution is indeed not detected in the high latitude oceans due to the presence of decadal mode of variability. In the low latitude oceans instead, the weaker fluctuations of ocean carbon fluxes at decadal time scale favor the detection of climate influence in the recent variations of the CO 2 fluxes. (author) [fr

  11. Deep ocean ventilation, carbon isotopes, marine sedimentation and the deglacial CO2 rise

    Directory of Open Access Journals (Sweden)

    C. Heinze

    2011-07-01

    Full Text Available The link between the atmospheric CO2 level and the ventilation state of the deep ocean is an important building block of the key hypotheses put forth to explain glacial-interglacial CO2 fluctuations. In this study, we systematically examine the sensitivity of atmospheric CO2 and its carbon isotope composition to changes in deep ocean ventilation, the ocean carbon pumps, and sediment formation in a global 3-D ocean-sediment carbon cycle model. Our results provide support for the hypothesis that a break up of Southern Ocean stratification and invigorated deep ocean ventilation were the dominant drivers for the early deglacial CO2 rise of ~35 ppm between the Last Glacial Maximum and 14.6 ka BP. Another rise of 10 ppm until the end of the Holocene is attributed to carbonate compensation responding to the early deglacial change in ocean circulation. Our reasoning is based on a multi-proxy analysis which indicates that an acceleration of deep ocean ventilation during early deglaciation is not only consistent with recorded atmospheric CO2 but also with the reconstructed opal sedimentation peak in the Southern Ocean at around 16 ka BP, the record of atmospheric δ13CCO2, and the reconstructed changes in the Pacific CaCO3 saturation horizon.

  12. Distribution of planktonic biogenic carbonate organisms in the Southern Ocean south of Australia: a baseline for ocean acidification impact assessment

    Science.gov (United States)

    Trull, Thomas W.; Passmore, Abraham; Davies, Diana M.; Smit, Tim; Berry, Kate; Tilbrook, Bronte

    2018-01-01

    The Southern Ocean provides a vital service by absorbing about one-sixth of humankind's annual emissions of CO2. This comes with a cost - an increase in ocean acidity that is expected to have negative impacts on ocean ecosystems. The reduced ability of phytoplankton and zooplankton to precipitate carbonate shells is a clearly identified risk. The impact depends on the significance of these organisms in Southern Ocean ecosystems, but there is very little information on their abundance or distribution. To quantify their presence, we used coulometric measurement of particulate inorganic carbonate (PIC) on particles filtered from surface seawater into two size fractions: 50-1000 µm to capture foraminifera (the most important biogenic carbonate-forming zooplankton) and 1-50 µm to capture coccolithophores (the most important biogenic carbonate-forming phytoplankton). Ancillary measurements of biogenic silica (BSi) and particulate organic carbon (POC) provided context, as estimates of the biomass of diatoms (the highest biomass phytoplankton in polar waters) and total microbial biomass, respectively. Results for nine transects from Australia to Antarctica in 2008-2015 showed low levels of PIC compared to Northern Hemisphere polar waters. Coccolithophores slightly exceeded the biomass of diatoms in subantarctic waters, but their abundance decreased more than 30-fold poleward, while diatom abundances increased, so that on a molar basis PIC was only 1 % of BSi in Antarctic waters. This limited importance of coccolithophores in the Southern Ocean is further emphasized in terms of their associated POC, representing less than 1 % of total POC in Antarctic waters and less than 10 % in subantarctic waters. NASA satellite ocean-colour-based PIC estimates were in reasonable agreement with the shipboard results in subantarctic waters but greatly overestimated PIC in Antarctic waters. Contrastingly, the NASA Ocean Biogeochemical Model (NOBM) shows coccolithophores as overly

  13. Distribution of planktonic biogenic carbonate organisms in the Southern Ocean south of Australia: a baseline for ocean acidification impact assessment

    Directory of Open Access Journals (Sweden)

    T. W. Trull

    2018-01-01

    Full Text Available The Southern Ocean provides a vital service by absorbing about one-sixth of humankind's annual emissions of CO2. This comes with a cost – an increase in ocean acidity that is expected to have negative impacts on ocean ecosystems. The reduced ability of phytoplankton and zooplankton to precipitate carbonate shells is a clearly identified risk. The impact depends on the significance of these organisms in Southern Ocean ecosystems, but there is very little information on their abundance or distribution. To quantify their presence, we used coulometric measurement of particulate inorganic carbonate (PIC on particles filtered from surface seawater into two size fractions: 50–1000 µm to capture foraminifera (the most important biogenic carbonate-forming zooplankton and 1–50 µm to capture coccolithophores (the most important biogenic carbonate-forming phytoplankton. Ancillary measurements of biogenic silica (BSi and particulate organic carbon (POC provided context, as estimates of the biomass of diatoms (the highest biomass phytoplankton in polar waters and total microbial biomass, respectively. Results for nine transects from Australia to Antarctica in 2008–2015 showed low levels of PIC compared to Northern Hemisphere polar waters. Coccolithophores slightly exceeded the biomass of diatoms in subantarctic waters, but their abundance decreased more than 30-fold poleward, while diatom abundances increased, so that on a molar basis PIC was only 1 % of BSi in Antarctic waters. This limited importance of coccolithophores in the Southern Ocean is further emphasized in terms of their associated POC, representing less than 1 % of total POC in Antarctic waters and less than 10 % in subantarctic waters. NASA satellite ocean-colour-based PIC estimates were in reasonable agreement with the shipboard results in subantarctic waters but greatly overestimated PIC in Antarctic waters. Contrastingly, the NASA Ocean Biogeochemical Model (NOBM shows

  14. Vapor mercury uptake with sulphur impregnated active carbons derived using sulphur dioxide

    International Nuclear Information System (INIS)

    Tong, S.; Methta, H.; Ahmed, I.; Morris, E.; Fuentes de Maria, L.; Jia, C.Q.

    2008-01-01

    Active carbon adsorption is the primary technology used for removal of vapour mercury from flue gases in coal-fired power plants, municipal solid waste combustors, and other sources. It can be carried out using two different processes, notably injection of powder active carbon into flue gas streams upstream of the particulate collection devices, and filtration with a granular active carbon fixed bed downstream of the flue gas desulphurization units and/or particulate collectors. This paper presented an investigation of vapour mercury uptake performance of laboratory-made sulphur impregnated active carbons (SIACs) using a fixed bed reactor in a temperature range of 25 to 200 degrees Celsius. The materials and methods as well as the properties of activated carbons studied were presented. The experimental set-up was also described. The paper discussed the effects of initial concentration, the flow rate, the loading amount of SIACs, temperature, and the sulphur impregnation on the mercury uptake performance. The study showed that SIACs produced with sulphur dioxide exhibited a more complicated behaviour when temperature was varied, implying a mixed adsorption mechanism. 10 refs., 3 tabs., 8 figs

  15. Responses of the ocean carbon cycle to climate change: Results from an earth system climate model simulation

    Institute of Scientific and Technical Information of China (English)

    WANG Shuang-Jing; CAO Long; LI Na

    2014-01-01

    Based on simulations using the University of Victoria’s Earth System Climate Model, we analyzed the responses of the ocean carbon cycle to increasing atmospheric CO2 levels and climate change from 1800 to 2500 following the RCP 8.5 scenario and its extension. Compared to simulations without climate change, the simulation with a climate sensitivity of 3.0 K shows that in 2100, due to increased atmospheric CO2 concentrations, the simulated sea surface temperature increases by 2.7 K, the intensity of the North Atlantic deep water formation reduces by4.5 Sv, and the oceanic uptake of anthropogenic CO2 decreases by 0.8 Pg C. Climate change is also found to have a large effect on the North Atlantic’s ocean column inventory of anthropogenic CO2. Between the years 1800 and 2500, compared with the simulation with no climate change, the simulation with climate change causes a reduction in the total anthropogenic CO2 column inventory over the entire ocean and in North Atlantic by 23.1% and 32.0%, respectively. A set of simulations with climate sensitivity variations from 0.5 K to 4.5 K show that with greater climate sensitivity climate change would have a greater effect in reducing the ocean’s ability to absorb CO2 from the atmosphere.

  16. Light Conditions Affect the Measurement of Oceanic Bacterial Production via Leucine Uptake

    Science.gov (United States)

    Morán, Xosé Anxelu G.; Massana, Ramon; Gasol, Josep M.

    2001-01-01

    The effect of irradiance in the range of 400 to 700 nm or photosynthetically active radiation (PAR) on bacterial heterotrophic production estimated by the incorporation of 3H-leucine (referred to herein as Leu) was investigated in the northwestern Mediterranean Sea and in a coastal North Atlantic site, with Leu uptake rates ranging over 3 orders of magnitude. We performed in situ incubations under natural irradiance levels of Mediterranean samples taken from five depths around solar noon and compared them to incubations in the dark. In two of the three stations large differences were found between light and dark uptake rates for the surfacemost samples, with dark values being on average 133 and 109% higher than in situ ones. Data obtained in coastal North Atlantic waters confirmed that dark enclosure may increase Leu uptake rates more than threefold. To explain these differences, on-board experiments of Leu uptake versus irradiance were performed with Mediterranean samples from depths of 5 and 40 m. Incubations under a gradient of 12 to 1,731 μmol of photons m−2 s−1 evidenced a significant increase in incorporation rates with increasing PAR in most of the experiments, with dark-incubated samples departing from this pattern. These results were not attributed to inhibition of Leu uptake in the light but to enhanced bacterial response when transferred to dark conditions. The ratio of dark to light uptake rates increased as dissolved inorganic nitrogen concentrations decreased, suggesting that bacterial nutrient deficiency was overcome by some process occurring only in the dark bottles. PMID:11525969

  17. Respiration of new and old carbon in the surface ocean: Implications for estimates of global oceanic gross primary productivity

    Science.gov (United States)

    Carvalho, Matheus C.; Schulz, Kai G.; Eyre, Bradley D.

    2017-06-01

    New respiration (Rnew, of freshly fixated carbon) and old respiration (Rold, of storage carbon) were estimated for different regions of the global surface ocean using published data on simultaneous measurements of the following: (1) primary productivity using 14C (14PP); (2) gross primary productivity (GPP) based on 18O or O2; and (3) net community productivity (NCP) using O2. The ratio Rnew/GPP in 24 h incubations was typically between 0.1 and 0.3 regardless of depth and geographical area, demonstrating that values were almost constant regardless of large variations in temperature (0 to 27°C), irradiance (surface to 100 m deep), nutrients (nutrient-rich and nutrient-poor waters), and community composition (diatoms, flagellates, etc,). As such, between 10 and 30% of primary production in the surface ocean is respired in less than 24 h, and most respiration (between 55 and 75%) was of older carbon. Rnew was most likely associated with autotrophs, with minor contribution from heterotrophic bacteria. Patterns were less clear for Rold. Short 14C incubations are less affected by respiratory losses. Global oceanic GPP is estimated to be between 70 and 145 Gt C yr-1.Plain Language SummaryHere we present a comprehensive coverage of ocean new and old respiration. Our results show that nearly 20% of oceanic gross primary production is consumed in the first 24 h. However, most (about 60%) respiration is of older carbon fixed at least 24 h before its consumption. Rates of new respiration relative to gross primary production were remarkably constant for the entire ocean, which allowed a preliminary estimation of global primary productivity as between 70 and 145 gt C yr-1.

  18. Natural Ocean Carbon Cycle Sensitivity to Parameterizations of the Recycling in a Climate Model

    Science.gov (United States)

    Romanou, A.; Romanski, J.; Gregg, W. W.

    2014-01-01

    Sensitivities of the oceanic biological pump within the GISS (Goddard Institute for Space Studies ) climate modeling system are explored here. Results are presented from twin control simulations of the air-sea CO2 gas exchange using two different ocean models coupled to the same atmosphere. The two ocean models (Russell ocean model and Hybrid Coordinate Ocean Model, HYCOM) use different vertical coordinate systems, and therefore different representations of column physics. Both variants of the GISS climate model are coupled to the same ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM), which computes prognostic distributions for biotic and abiotic fields that influence the air-sea flux of CO2 and the deep ocean carbon transport and storage. In particular, the model differences due to remineralization rate changes are compared to differences attributed to physical processes modeled differently in the two ocean models such as ventilation, mixing, eddy stirring and vertical advection. GISSEH(GISSER) is found to underestimate mixed layer depth compared to observations by about 55% (10 %) in the Southern Ocean and overestimate it by about 17% (underestimate by 2%) in the northern high latitudes. Everywhere else in the global ocean, the two models underestimate the surface mixing by about 12-34 %, which prevents deep nutrients from reaching the surface and promoting primary production there. Consequently, carbon export is reduced because of reduced production at the surface. Furthermore, carbon export is particularly sensitive to remineralization rate changes in the frontal regions of the subtropical gyres and at the Equator and this sensitivity in the model is much higher than the sensitivity to physical processes such as vertical mixing, vertical advection and mesoscale eddy transport. At depth, GISSER, which has a significant warm bias, remineralizes nutrients and carbon faster thereby producing more nutrients and carbon at depth, which

  19. Tracing Carbon Cycling in the Atmosphere and Oceans During the Cretaceous Ocean Anoxic Event 2 (OAE2, 94Ma)

    Science.gov (United States)

    Moran, S. A. M.; Boudinot, F. G.; Dildar, N.; Sepúlveda, J.

    2017-12-01

    We present a high-resolution record of compound-specific stable carbon isotope data from short-chain—aquatic algae—and long-chain n-alkanes—terrestrial plants—preserved in sedimentary sequences from the Smokey Hollow #1 (SH1) core in the Grand Staircase Escalante National Monument in southern Utah. The study area covered by SH1 core was situated at the western margin of the Western Interior Seaway during the Cretaceous Ocean Anoxic Event (OAE2, 94Ma.), and was characterized by high sedimentation rates and enhanced preservation of both marine and terrestrial organic matter. Short- and long-chain n-alkanes were isolated and purified from branched and cyclic aliphatic hydrocarbons using an optimized urea adduction protocol, and δ13Cn-alkane was measured using a Thermo MAT253 GC-C-IR-MS. We use the δ13Cn-alkane from aquatic and terrestrial sources to better understand carbon cycle interactions in the oceanic and atmospheric carbon pools across this event. Our results indicate that the δ13C of terrestrial plants experienced a faster and more pronounced positive carbon isotope excursion compared to marine sources. We will discuss how these results can inform models of carbon cycle interactions between the ocean and the atmosphere during greenhouse climates, and how they can be used to trace possible sources of CO2.

  20. Mangroves, a major source of dissolved organic carbon to the oceans

    Science.gov (United States)

    Dittmar, Thorsten; Hertkorn, Norbert; Kattner, Gerhard; Lara, RubéN. J.

    2006-03-01

    Organic matter, which is dissolved in low concentrations in the vast waters of the oceans, contains a total amount of carbon similar to atmospheric carbon dioxide. To understand global biogeochemical cycles, it is crucial to quantify the sources of marine dissolved organic carbon (DOC). We investigated the impact of mangroves, the dominant intertidal vegetation of the tropics, on marine DOC inventories. Stable carbon isotopes and proton nuclear magnetic resonance spectroscopy showed that mangroves are the main source of terrigenous DOC in the open ocean off northern Brazil. Sunlight efficiently destroyed aromatic molecules during transport offshore, removing about one third of mangrove-derived DOC. The remainder was refractory and may thus be distributed over the oceans. On a global scale, we estimate that mangroves account for >10% of the terrestrially derived, refractory DOC transported to the ocean, while they cover only <0.1% of the continents' surface.

  1. Response to Comment on "Dilution limits dissolved organic carbon utilization in the deep ocean"

    KAUST Repository

    Arrieta, J M; Mayol, E.; Hansman, R. L.; Herndl, G. J.; Dittmar, T.; Duarte, Carlos M.

    2015-01-01

    Our recent finding that dilution limits dissolved organic carbon (DOC) utilization in the deep ocean has been criticized based on the common misconception that lability equates to rapid and complete utilization. Even when considering

  2. Forest canopy uptake of atmospheric nitrogen deposition at eastern U.S. conifer sites: Carbon storage implications?

    Science.gov (United States)

    Herman Sievering; Ivan Fernandez; John Lee; John Hom; Lindsey Rustad

    2000-01-01

    Dry deposition determinations, along with wet deposition and throughfall (TF) measurements, at a spruce fir forest in central Maine were used to estimate the effect of atmospherically deposited nitrogen (N) uptake on forest carbon storage. Using nitric acid and particulate N as well as TF ammonium and nitrate data, the growing season (May-October) net canopy uptake of...

  3. Input of particulate organic and dissolved inorganic carbon from the Amazon to the Atlantic Ocean

    OpenAIRE

    Druffel, E. R. M; Bauer, J. E; Griffin, S.

    2005-01-01

    We report concentrations and isotope measurements (radiocarbon and stable carbon) of dissolved inorganic carbon (DIC) and suspended particulate organic carbon (POC) in waters collected from the mouth of the Amazon River and the North Brazil Current. Samples were collected in November 1991, when the Amazon hydrograph was at its annual minimum and the North Brazil Current had retroflected into the equatorial North Atlantic. The DIC Δ14C results revealed postbomb carbon in river and ocean waters...

  4. Photochemical mineralization of terrigenous DOC to dissolved inorganic carbon in ocean

    OpenAIRE

    Aarnos, Hanna; Gélinas, Yves; Kasurinen, Ville; Gu, Yufei; Puupponen, Veli-Mikko; Vähätalo, Anssi

    2018-01-01

    When terrigenous dissolved organic carbon (tDOC) rich in chromophoric dissolved organic matter (tCDOM) enters the ocean, solar radiation mineralizes it partially into dissolved inorganic carbon (DIC). This study addresses the amount and the rates of DIC photoproduction from tDOC and the area of ocean required to photomineralize tDOC. We collected water samples from 10 major rivers, mixed them with artificial seawater, and irradiated them with simulated solar radiation to measure DIC photoprod...

  5. NW European shelf under climate warming: implications for open ocean – shelf exchange, primary production, and carbon absorption

    Directory of Open Access Journals (Sweden)

    M. Gröger

    2013-06-01

    Full Text Available Shelves have been estimated to account for more than one-fifth of the global marine primary production. It has been also conjectured that shelves strongly influence the oceanic absorption of anthropogenic CO2 (carbon shelf pump. Owing to their coarse resolution, currently applied global climate models are inappropriate to investigate the impact of climate change on shelves and regional models do not account for the complex interaction with the adjacent open ocean. In this study, a global ocean general circulation model and biogeochemistry model were set up with a distorted grid providing a maximal resolution for the NW European shelf and the adjacent northeast Atlantic. Using model climate projections we found that already a~moderate warming of about 2.0 K of the sea surface is linked with a reduction by ~ 30% of the biological production on the NW European shelf. If we consider the decline of anthropogenic riverine eutrophication since the 1990s, the reduction of biological production amounts is even larger. The relative decline of NW European shelf productivity is twice as strong as the decline in the open ocean (~ 15%. The underlying mechanism is a spatially well confined stratification feedback along the continental shelf break. This feedback reduces the nutrient supply from the deep Atlantic to about 50%. In turn, the reduced productivity draws down CO2 absorption in the North Sea by ~ 34% at the end of the 21st century compared to the end of the 20th century implying a strong weakening of shelf carbon pumping. Sensitivity experiments with diagnostic tracers indicate that not more than 20% of the carbon absorbed in the North Sea contributes to the long-term carbon uptake of the world ocean. The rest remains within the ocean's mixed layer where it is exposed to the atmosphere. The predicted decline in biological productivity, and decrease of phytoplankton concentration (in the North Sea by averaged 25% due to reduced nutrient imports from

  6. Inter-annual variation of carbon uptake by a plantation oak woodland in south-eastern England

    Directory of Open Access Journals (Sweden)

    M. Wilkinson

    2012-12-01

    Full Text Available The carbon balance of an 80-yr-old deciduous oak plantation in the temperate oceanic climate of the south-east of Great Britain was measured by eddy covariance over 12 yr (1999–2010. The mean annual net ecosystem productivity (NEP was 486 g C m−2 yr−1 (95% CI of ±73 g C m−2 yr−1, and this was partitioned into a gross primary productivity (GPP of 2034 ± 145 g C m−2 yr−1, over a 165 (±6 day growing season, and an annual loss of carbon through respiration and decomposition (ecosystem respiration, Reco of 1548 ± 122 g C m−2 yr−1. Although the maximum variation of NEP between years was large (333 g C m−2 yr−1, the ratio of Reco/GPP remained relatively constant (0.76 ± 0.02 CI. Some anomalies in the annual patterns of the carbon balance could be linked to particular weather events, such as low summer solar radiation and low soil moisture content (values below 30% by volume. The European-wide heat wave and drought of 2003 did not reduce the NEP of this woodland because of good water supply from the surface-water gley soil. The inter-annual variation in estimated intercepted radiation only accounted for ~ 47% of the variation in GPP, although a significant relationship (p < 0.001 was found between peak leaf area index and annual GPP, which modified the efficiency with which incident radiation was used in net CO2 uptake. Whilst the spring start and late autumn end of the net CO2 uptake period varied substantially (range of 24 and 27 days respectively, annual GPP was not related to growing season length. Severe outbreaks of defoliating moth caterpillars, mostly Tortrix viridana L. and Operophtera brumata L., caused considerable damage to the forest canopy in 2009 and 2010, resulting in reduced GPP in these two years. Inter-annual variation in

  7. The biological carbon pump in the ocean: Reviewing model representations and its feedbacks on climate perturbations.

    Science.gov (United States)

    Hülse, Dominik; Arndt, Sandra; Ridgwell, Andy; Wilson, Jamie

    2016-04-01

    The ocean-sediment system, as the biggest carbon reservoir in the Earth's carbon cycle, plays a crucial role in regulating atmospheric carbon dioxide concentrations and climate. Therefore, it is essential to constrain the importance of marine carbon cycle feedbacks on global warming and ocean acidification. Arguably, the most important single component of the ocean's carbon cycle is the so-called "biological carbon pump". It transports carbon that is fixed in the light-flooded surface layer of the ocean to the deep ocean and the surface sediment, where it is degraded/dissolved or finally buried in the deep sediments. Over the past decade, progress has been made in understanding different factors that control the efficiency of the biological carbon pump and their feedbacks on the global carbon cycle and climate (i.e. ballasting = ocean acidification feedback; temperature dependant organic matter degradation = global warming feedback; organic matter sulphurisation = anoxia/euxinia feedback). Nevertheless, many uncertainties concerning the interplay of these processes and/or their relative significance remain. In addition, current Earth System Models tend to employ empirical and static parameterisations of the biological pump. As these parametric representations are derived from a limited set of present-day observations, their ability to represent carbon cycle feedbacks under changing climate conditions is limited. The aim of my research is to combine past carbon cycling information with a spatially resolved global biogeochemical model to constrain the functioning of the biological pump and to base its mathematical representation on a more mechanistic approach. Here, I will discuss important aspects that control the efficiency of the ocean's biological carbon pump, review how these processes of first order importance are mathematically represented in existing Earth system Models of Intermediate Complexity (EMIC) and distinguish different approaches to approximate

  8. Oxygen in the deep-sea: The challenge of maintaining uptake rates in a changing ocean

    Science.gov (United States)

    Hofmann, A. F.; Peltzer, E. T.; Brewer, P. G.

    2011-12-01

    Although focused on recently, ocean acidification is not the only effect of anthropogenic CO2 emissions on the ocean. Ocean warming will reduce dissolved oxygen concentrations and at the hypoxic limit for a given species this can pose challenges to marine life. The limit is traditionally reported simply as the static mass concentration property [O2]; here we treat it as a dynamic gas exchange problem for the animal analogous to gas exchange at the sea surface. The diffusive limit and its relationship to water velocity is critical for the earliest stages of marine life (eggs, embryos), but the effect is present for all animals at all stages of life. We calculate the external limiting O2 conditions for several representative metabolic rates and their relationship to flow of the bulk fluid under different environmental conditions. Ocean O2 concentrations decline by ≈ 14 μmol kg-1 for a 2 °C rise in temperature. At standard 1000 m depth conditions in the Pacific, flow over the surface would have to increase by ≈ 60% from 2.0 to 3.2 cm s-1 to compensate for this change. The functions derived allow new calculations of depth profiles of limiting O2 concentrations, as well as maximal diffusively sustainable metabolic oxygen consumption rates at various places around the world. Our treatment shows that there is a large variability in the global ocean in terms of facilitating aerobic life. This variability is greater than the variability of the oxygen concentration alone. It becomes clear that temperature and pressure dependencies of diffusion and partial pressure create a region typically around 1000 m depth where a maximal [O2] is needed to sustain a given metabolic rate. This zone of greatest physical constriction on the diffusive transport in the boundary layer is broadly consistent with the oxygen minimum zone, i.e., the zone of least oxygen concentration supply, resulting in a pronounced minimum of maximal diffusively sustainable metabolic oxygen consumption

  9. Bicarbonate uptake via an anion exchange protein is the main mechanism of inorganic carbon acquisition by the giant kelp Macrocystis pyrifera (Laminariales, Phaeophyceae) under variable pH.

    Science.gov (United States)

    Fernández, Pamela A; Hurd, Catriona L; Roleda, Michael Y

    2014-12-01

    Macrocystis pyrifera is a widely distributed, highly productive, seaweed. It is known to use bicarbonate (HCO3 (-) ) from seawater in photosynthesis and the main mechanism of utilization is attributed to the external catalyzed dehydration of HCO3 (-) by the surface-bound enzyme carbonic anhydrase (CAext ). Here, we examined other putative HCO3 (-) uptake mechanisms in M. pyrifera under pHT 9.00 (HCO3 (-) : CO2  = 940:1) and pHT 7.65 (HCO3 (-) : CO2  = 51:1). Rates of photosynthesis, and internal CA (CAint ) and CAext activity were measured following the application of AZ which inhibits CAext , and DIDS which inhibits a different HCO3 (-) uptake system, via an anion exchange (AE) protein. We found that the main mechanism of HCO3 (-) uptake by M. pyrifera is via an AE protein, regardless of the HCO3 (-) : CO2 ratio, with CAext making little contribution. Inhibiting the AE protein led to a 55%-65% decrease in photosynthetic rates. Inhibiting both the AE protein and CAext at pHT 9.00 led to 80%-100% inhibition of photosynthesis, whereas at pHT 7.65, passive CO2 diffusion supported 33% of photosynthesis. CAint was active at pHT 7.65 and 9.00, and activity was always higher than CAext , because of its role in dehydrating HCO3 (-) to supply CO2 to RuBisCO. Interestingly, the main mechanism of HCO3 (-) uptake in M. pyrifera was different than that in other Laminariales studied (CAext -catalyzed reaction) and we suggest that species-specific knowledge of carbon uptake mechanisms is required in order to elucidate how seaweeds might respond to future changes in HCO3 (-) :CO2 due to ocean acidification. © 2014 Phycological Society of America.

  10. Long-term ocean oxygen depletion in response to carbon dioxide emissions from fossil fuels

    DEFF Research Database (Denmark)

    Shaffer, G.; Olsen, S.M.; Pedersen, Jens Olaf Pepke

    2009-01-01

    Ongoing global warming could persist far into the future, because natural processes require decades to hundreds of thousands of years to remove carbon dioxide from fossil-fuel burning from the atmosphere(1-3). Future warming may have large global impacts including ocean oxygen depletion and assoc......Ongoing global warming could persist far into the future, because natural processes require decades to hundreds of thousands of years to remove carbon dioxide from fossil-fuel burning from the atmosphere(1-3). Future warming may have large global impacts including ocean oxygen depletion...... solubility from surface-layer warming accounts for most of the enhanced oxygen depletion in the upper 500 m of the ocean. Possible weakening of ocean overturning and convection lead to further oxygen depletion, also in the deep ocean. We conclude that substantial reductions in fossil-fuel use over the next...

  11. Improving representation of nitrogen uptake, allocation, and carbon assimilation in the Community Land Model

    Science.gov (United States)

    Ghimire, B.; Riley, W. J.; Koven, C.

    2013-12-01

    Nitrogen is the most important nutrient limiting plant carbon assimilation and growth, and is required for production of photosynthetic enzymes, growth and maintenance respiration, and maintaining cell structure. The forecasted rise in plant available nitrogen through atmospheric nitrogen deposition and the release of locked soil nitrogen by permafrost thaw in high latitude ecosystems is likely to result in an increase in plant productivity. However a mechanistic representation of plant nitrogen dynamics is lacking in earth system models. Most earth system models ignore the dynamic nature of plant nutrient uptake and allocation, and further lack tight coupling of below- and above-ground processes. In these models, the increase in nitrogen uptake does not translate to a corresponding increase in photosynthesis parameters, such as maximum Rubisco capacity and electron transfer rate. We present an improved modeling framework implemented in the Community Land Model version 4.5 (CLM4.5) for dynamic plant nutrient uptake, and allocation to different plant parts, including leaf enzymes. This modeling framework relies on imposing a more realistic flexible carbon to nitrogen stoichiometric ratio for different plant parts. The model mechanistically responds to plant nitrogen uptake and leaf allocation though changes in photosynthesis parameters. We produce global simulations, and examine the impacts of the improved nitrogen cycling. The improved model is evaluated against multiple observations including TRY database of global plant traits, nitrogen fertilization observations and 15N tracer studies. Global simulations with this new version of CLM4.5 showed better agreement with the observations than the default CLM4.5-CN model, and captured the underlying mechanisms associated with plant nitrogen cycle.

  12. Changes in ocean circulation and carbon storage are decoupled from air-sea CO2 fluxes

    Directory of Open Access Journals (Sweden)

    A. Gnanadesikan

    2011-02-01

    Full Text Available The spatial distribution of the air-sea flux of carbon dioxide is a poor indicator of the underlying ocean circulation and of ocean carbon storage. The weak dependence on circulation arises because mixing-driven changes in solubility-driven and biologically-driven air-sea fluxes largely cancel out. This cancellation occurs because mixing driven increases in the poleward residual mean circulation result in more transport of both remineralized nutrients and heat from low to high latitudes. By contrast, increasing vertical mixing decreases the storage associated with both the biological and solubility pumps, as it decreases remineralized carbon storage in the deep ocean and warms the ocean as a whole.

  13. Major role of nitrite-oxidizing bacteria in dark ocean carbon fixation

    NARCIS (Netherlands)

    Pachiadaki, M.G.; Sintes, E.; Bergauer, K.; Brown, J.M.; Record, N.R.; Swan, B.K.; Mathyer, M.E.; Hallam, S.J.; López-Garcìa, P.; Takaki, Y.; Nunoura, T.; Woyke, T.; Herndl, G.J.; Stepanauskas, R.

    2017-01-01

    Carbon fixation by chemoautotrophic microorganisms in the dark ocean has a major impact on global carbon cycling and ecological relationships in the ocean’s interior, but the relevant taxa and energy sources remain enigmatic.We show evidence that nitrite-oxidizing bacteria affiliated with the

  14. Contributions of secondary forest and nitrogen dynamics to terrestrial carbon uptake

    Directory of Open Access Journals (Sweden)

    X. Yang

    2010-10-01

    Full Text Available We use a terrestrial carbon-nitrogen cycle component of the Integrated Science Assessment Model (ISAM to investigate the impacts of nitrogen dynamics on regrowing secondary forests over the 20th century. We further examine what the impacts of nitrogen deposition and land use change history are on terrestrial carbon uptake since preindustrial time. Our results suggest that global total net land use emissions for the 1990s associated with changes in cropland, pastureland, and wood harvest are 1.22 GtC/yr. Without considering the secondary forest regrowth, the estimated net global total land use emissions are 1.58 GtC/yr or about 0.36 GtC/yr higher than if secondary forest regrowth is considered. Results also show that without considering the nitrogen dynamics and deposition, the estimated global total secondary forest sink for the 1990s is 0.90 GtC/yr or about 0.54 GtC/yr higher than estimates that include the impacts of nitrogen dynamics and deposition. Nitrogen deposition alone is responsible for about 0.13 GtC/yr of the total secondary forest sink. While nitrogen is not a limiting nutrient in the intact primary forests in tropical regions, our study suggests that nitrogen becomes a limiting nutrient for regrowing secondary forests of the tropical regions, in particular Latin America and Tropical Africa. This is because land use change activities, especially wood harvest, removes large amounts of nitrogen from the system when slash is burnt or wood is removed for harvest. However, our model results show that carbon uptake is enhanced in the tropical secondary forests of the Indian region. We argue that this may be due to enhanced nitrogen mineralization and increased nitrogen availability following land use change in the Indian tropical forest ecosystems. Results also demonstrate that there is a significant amount of carbon accumulating in the Northern Hemisphere where most land use changes and forest regrowth has occurred in recent decades

  15. Physiological responses by juvenile Egregia menziesii (Phaeophyta) to simulated effects of wave action: Carbon and nitrogen uptake and carbon partitioning

    International Nuclear Information System (INIS)

    Kraemer, G.P.

    1990-01-01

    Although biomechanical and morphological adaptations to different wave energy regimes are well known, the physiological mechanisms behind, and the trigger(s) eliciting these responses, are not. Egregia menziesii (Turn.) Aresch. juveniles (5-10 cm) were incubated for 4 hr in chambers containing 14 C-labeled bicarbonate, under combinations of two levels of nutrient concentration and two levels of tensile force. Whole tissue and cell wall material (=cellulose + alginates) were examined for 14 C incorporation. Tensile force elicited greater incorporation into whole tissue and directed more carbon into the cell wall compartment. Ambient nutrient levels and tissue age both had inverse effects on carbon partitioning into cell wall material. Tensile force also reduced nitrate uptake rates by about 50%

  16. A Possible Late Paleocene-Early Eocene Ocean Acidification Event Recoded in the Adriatic Carbonate Platform

    Science.gov (United States)

    Weiss, A.; Martindale, R. C.; Kosir, A.; Oefinger, J.

    2017-12-01

    The Paleocene-Eocene Thermal Maximum (PETM) event ( 56.3 Ma) was a period of massive carbon release into the Earth system, resulting in significant shifts in ocean chemistry. It has been proposed that ocean acidification - a decrease in the pH and carbonate saturation state of the water as a result of dissolved carbon dioxide in sea water - occurred in both the shallow and deep marine realms. Ocean acidification would have had a devastating impact on the benthic ecosystem, and has been proposed as the cause of decreased carbonate deposition in marine sections and coral reef collapse during the late Paleocene. To date, however, the only physical evidence of Paleocene-Eocene ocean acidification has been shown for offshore sites (i.e., a shallow carbonate compensation depth), but isotope analysis (i.e. B, I/Ca) suggests that acidification occurred in the shallow shelves as well. Several sites in the Kras region of Slovenia, has been found to contain apparent erosion surfaces coeval with the Paleocene-Eocene Boundary. We have investigated these potentially acidified horizons using petrography, stable carbon isotopes, cathodoluminescence, and elemental mapping. These datasets will inform whether the horizons formed by seafloor dissolution in an acidified ocean, or are due to subaerial exposure, or burial diagenesis (i.e. stylotization). Physical erosion and diagenesis can easily be ruled out based on field relationships and petrography, but the other potential causes must be analyzed more critically.

  17. The acceleration of dissolved cobalt's ecological stoichiometry due to biological uptake, remineralization, and scavenging in the Atlantic Ocean

    Science.gov (United States)

    Saito, Mak A.; Noble, Abigail E.; Hawco, Nicholas; Twining, Benjamin S.; Ohnemus, Daniel C.; John, Seth G.; Lam, Phoebe; Conway, Tim M.; Johnson, Rod; Moran, Dawn; McIlvin, Matthew

    2017-10-01

    The stoichiometry of biological components and their influence on dissolved distributions have long been of interest in the study of the oceans. Cobalt has the smallest oceanic inventory of inorganic micronutrients and hence is particularly vulnerable to influence by internal oceanic processes including euphotic zone uptake, remineralization, and scavenging. Here we observe not only large variations in dCo : P stoichiometry but also the acceleration of those dCo : P ratios in the upper water column in response to several environmental processes. The ecological stoichiometry of total dissolved cobalt (dCo) was examined using data from a US North Atlantic GEOTRACES transect and from a zonal South Atlantic GEOTRACES-compliant transect (GA03/3e and GAc01) by Redfieldian analysis of its statistical relationships with the macronutrient phosphate. Trends in the dissolved cobalt to phosphate (dCo : P) stoichiometric relationships were evident in the basin-scale vertical structure of cobalt, with positive dCo : P slopes in the euphotic zone and negative slopes found in the ocean interior and in coastal environments. The euphotic positive slopes were often found to accelerate towards the surface and this was interpreted as being due to the combined influence of depleted phosphate, phosphorus-sparing (conserving) mechanisms, increased alkaline phosphatase metalloenzyme production (a zinc or perhaps cobalt enzyme), and biochemical substitution of Co for depleted Zn. Consistent with this, dissolved Zn (dZn) was found to be drawn down to only 2-fold more than dCo, despite being more than 18-fold more abundant in the ocean interior. Particulate cobalt concentrations increased in abundance from the base of the euphotic zone to become ˜ 10 % of the overall cobalt inventory in the upper euphotic zone with high stoichiometric values of ˜ 400 µmol Co mol-1 P. Metaproteomic results from the Bermuda Atlantic Time-series Study (BATS) station found cyanobacterial isoforms of the

  18. Carbon uptake by mature Amazon forests has mitigated Amazon nations' carbon emissions.

    Science.gov (United States)

    Phillips, Oliver L; Brienen, Roel J W

    2017-12-01

    Several independent lines of evidence suggest that Amazon forests have provided a significant carbon sink service, and also that the Amazon carbon sink in intact, mature forests may now be threatened as a result of different processes. There has however been no work done to quantify non-land-use-change forest carbon fluxes on a national basis within Amazonia, or to place these national fluxes and their possible changes in the context of the major anthropogenic carbon fluxes in the region. Here we present a first attempt to interpret results from ground-based monitoring of mature forest carbon fluxes in a biogeographically, politically, and temporally differentiated way. Specifically, using results from a large long-term network of forest plots, we estimate the Amazon biomass carbon balance over the last three decades for the different regions and nine nations of Amazonia, and evaluate the magnitude and trajectory of these differentiated balances in relation to major national anthropogenic carbon emissions. The sink of carbon into mature forests has been remarkably geographically ubiquitous across Amazonia, being substantial and persistent in each of the five biogeographic regions within Amazonia. Between 1980 and 2010, it has more than mitigated the fossil fuel emissions of every single national economy, except that of Venezuela. For most nations (Bolivia, Colombia, Ecuador, French Guiana, Guyana, Peru, Suriname) the sink has probably additionally mitigated all anthropogenic carbon emissions due to Amazon deforestation and other land use change. While the sink has weakened in some regions since 2000, our analysis suggests that Amazon nations which are able to conserve large areas of natural and semi-natural landscape still contribute globally-significant carbon sequestration. Mature forests across all of Amazonia have contributed significantly to mitigating climate change for decades. Yet Amazon nations have not directly benefited from providing this global scale

  19. Enhanced CO2 uptake at a shallow Arctic Ocean seep field overwhelms the positive warming potential of emitted methane.

    Science.gov (United States)

    Pohlman, John W; Greinert, Jens; Ruppel, Carolyn; Silyakova, Anna; Vielstädte, Lisa; Casso, Michael; Mienert, Jürgen; Bünz, Stefan

    2017-05-23

    Continued warming of the Arctic Ocean in coming decades is projected to trigger the release of teragrams (1 Tg = 10 6 tons) of methane from thawing subsea permafrost on shallow continental shelves and dissociation of methane hydrate on upper continental slopes. On the shallow shelves (shallow ebullitive methane seep field on the Svalbard margin reveal atmospheric CO 2 uptake rates (-33,300 ± 7,900 μmol m -2 ⋅d -1 ) twice that of surrounding waters and ∼1,900 times greater than the diffusive sea-air methane efflux (17.3 ± 4.8 μmol m -2 ⋅d -1 ). The negative radiative forcing expected from this CO 2 uptake is up to 231 times greater than the positive radiative forcing from the methane emissions. Surface water characteristics (e.g., high dissolved oxygen, high pH, and enrichment of 13 C in CO 2 ) indicate that upwelling of cold, nutrient-rich water from near the seafloor accompanies methane emissions and stimulates CO 2 consumption by photosynthesizing phytoplankton. These findings challenge the widely held perception that areas characterized by shallow-water methane seeps and/or strongly elevated sea-air methane flux always increase the global atmospheric greenhouse gas burden.

  20. Effect of long-term drought on carbon allocation and nitrogen uptake of Pinus sylvestris seedlings

    Science.gov (United States)

    Pumpanen, Jukka; Aaltonen, Heidi; Lindén, Aki; Köster, Kajar; Biasi, Christina; Heinonsalo, Jussi

    2015-04-01

    Weather extremes such as drought events are expected to increase in the future as a result of climate change. The drought affects the allocation of carbon assimilated by plants e.g. by modifying the root to shoot ratio, amount of fine roots and the amount of mycorrhizal fungal hyphae. We studied the effect of long term drought on the allocation of carbon in a common garden experiment with 4-year-old Pinus sylvestris seedlings. Half of the seedlings were exposed to long-term drought by setting the soil water content close to wilting point for over two growing seasons whereas the other half was grown in soil close to field capacity. We conducted a pulse labelling with 13CO2 in the end of the study by injecting a known amount of 13C enriched CO2 to the seedlings and measuring the CO2 uptake and distribution of 13C to the biomass of the seedlings and to the root and rhizosphere respiration. In addition, we studied the effect of drought on the decomposition of needle litter and uptake of nitrogen by 15N labelled needles buried in the soil in litter bags. The litterbags were collected and harvested in the end of the experiment and the changes in microbial community in the litterbags were studied from the phospholipid fatty acid (PLFA) composition. We also determined the 15N isotope concentrations from the needles of the seedlings to study the effect of drought on the nitrogen uptake of the seedlings. Our results indicate that the drought had a significant effect both on the biomass allocation of the seedlings and on the microbial species composition. The amount of carbon allocated belowground was much higher in the seedlings exposed to drought compared to the control seedlings. The seedlings seemed to adapt their carbon allocation to long-term drought to sustain adequate needle biomass and water uptake. The seedlings also adapted their osmotic potential and photosynthesis capacity to sustain the long-term drought as was indicated by the measurements of osmotic potential

  1. Potential effects of ocean acidification on Alaskan corals based on calcium carbonate mineralogy composition analysis (NCEI Accession 0157223)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This archival package contains potential effects of ocean acidification on Alaskan corals based on calcium carbonate mineralogy composition analysis. Effects of...

  2. Anthropogenic perturbation of the carbon fluxes from land to ocean

    KAUST Repository

    Regnier, Pierre; Friedlingstein, Pierre; Ciais, Philippe; Mackenzie, Fred T.; Gruber, Nicolas; Janssens, Ivan A.; Laruelle, Goulven G.; Lauerwald, Ronny; Luyssaert, Sebastiaan; Andersson, Andreas J.; Arndt, Sandra; Arnosti, Carol; Borges, Alberto V.; Dale, Andrew W.; Gallego-Sala, Angela; Goddé ris, Yves; Goossens, Nicolas; Hartmann, Jens; Heinze, Christoph; Ilyina, Tatiana; Joos, Fortunat; LaRowe, Douglas E.; Leifeld, Jens; Meysman, Filip J. R.; Munhoven, Guy; Raymond, Peter A.; Spahni, Renato; Suntharalingam, Parvadha; Thullner, Martin

    2013-01-01

    to enhanced carbon export from soils. Most of this additional carbon input to upstream rivers is either emitted back to the atmosphere as carbon dioxide (∼0.4 Pg C yr -1) or sequestered in sediments (∼0.5 Pg C yr -1) along the continuum of freshwater bodies

  3. An assessment of the inventory of Carbon-14 in the oceans

    International Nuclear Information System (INIS)

    Lassey, K.R.; Manning, M.R.; O'Brien, B.J.

    1987-04-01

    The oceanic inventory for natural 14 C is 19.6x10 29 atoms, an estimate similar to those found by other methods. The 14 C produced from nuclear weapons (1972) is 550x10 26 atoms and 52% was in the oceans. From 1972 to 1985 132x10 26 atoms of bomb 14 C were added. The nuclear power industry produces 0.5x10 26 atoms per year (17% of natural production rate). Most estimates by varying methods indicate an exchange time of carbon from atmosphere to ocean of about seven years or about 22 moles m -2 yr -1 for the surface ocean. The oceanic distribution generally has higher concentrations in low to mid latitudes, and low concentrations in the most southern regions, with the deep ocean retaining levels similar to those before nuclear testing

  4. Ocean Acidification: Investigation and Presentation of the Effects of Elevated Carbon Dioxide Levels on Seawater Chemistry and Calcareous Organisms

    Science.gov (United States)

    Buth, Jeffrey M.

    2016-01-01

    Ocean acidification refers to the process by which seawater absorbs carbon dioxide from the atmosphere, producing aqueous carbonic acid. Acidic conditions increase the solubility of calcium carbonate, threatening corals and other calcareous organisms that depend on it for protective structures. The global nature of ocean acidification and the…

  5. Edge effects enhance carbon uptake and its vulnerability to climate change in temperate broadleaf forests.

    Science.gov (United States)

    Reinmann, Andrew B; Hutyra, Lucy R

    2017-01-03

    Forest fragmentation is a ubiquitous, ongoing global phenomenon with profound impacts on the growing conditions of the world's remaining forest. The temperate broadleaf forest makes a large contribution to the global terrestrial carbon sink but is also the most heavily fragmented forest biome in the world. We use field measurements and geospatial analyses to characterize carbon dynamics in temperate broadleaf forest fragments. We show that forest growth and biomass increase by 89 ± 17% and 64 ± 12%, respectively, from the forest interior to edge, but ecosystem edge enhancements are not currently captured by models or approaches to quantifying regional C balance. To the extent that the findings from our research represent the forest of southern New England in the United States, we provide a preliminary estimate that edge growth enhancement could increase estimates of the region's carbon uptake and storage by 13 ± 3% and 10 ± 1%, respectively. However, we also find that forest growth near the edge declines three times faster than that in the interior in response to heat stress during the growing season. Using climate projections, we show that future heat stress could reduce the forest edge growth enhancement by one-third by the end of the century. These findings contrast studies of edge effects in the world's other major forest biomes and indicate that the strength of the temperate broadleaf forest carbon sink and its capacity to mitigate anthropogenic carbon emissions may be stronger, but also more sensitive to climate change than previous estimates suggest.

  6. Effects of ocean acidification on the physiological performance and carbon production of the Antarctic sea ice diatom Nitzschia sp. ICE-H.

    Science.gov (United States)

    Qu, Chang-Feng; Liu, Fang-Ming; Zheng, Zhou; Wang, Yi-Bin; Li, Xue-Gang; Yuan, Hua-Mao; Li, Ning; An, Mei-Ling; Wang, Xi-Xi; He, Ying-Ying; Li, Lu-Lu; Miao, Jin-Lai

    2017-07-15

    Ocean acidification (OA) resulting from increasing atmospheric CO 2 strongly influences marine ecosystems, particularly in the polar ocean due to greater CO 2 solubility. Here, we grew the Antarctic sea ice diatom Nitzschia sp. ICE-H in a semicontinuous culture under low (~400ppm) and high (1000ppm) CO 2 levels. Elevated CO 2 resulted in a stimulated physiological response including increased growth rates, chlorophyll a contents, and nitrogen and phosphorus uptake rates. Furthermore, high CO 2 enhanced cellular particulate organic carbon production rates, indicating a greater shift from inorganic to organic carbon. However, the cultures grown in high CO 2 conditions exhibited a decrease in both extracellular and intracellular carbonic anhydrase activity, suggesting that the carbon concentrating mechanisms of Nitzschia sp. ICE-H may be suppressed by elevated CO 2 . Our results revealed that OA would be beneficial to the survival of this sea ice diatom strain, with broad implications for global carbon cycles in the future ocean. Copyright © 2017. Published by Elsevier Ltd.

  7. Why Southern Ocean uptake of anthropogenic CO2 may be decreasing

    CSIR Research Space (South Africa)

    Mongwe, P

    2012-10-01

    Full Text Available to the warm surface water and its influence on CO2 solubility (Figures 2 and 3). The decline is DIC with depth correlates with the decrease in temperature (Figures 2 and 3), as colder water holds more CO2. The Southern Ocean has particularly high DIC... southwards, upwelling is also expected move more southwards, which may result in more intense CO2 outgassing. The emitted CO2 contributes to green house gases, which alter the heat balance and result in increased average temperatures. REFERENCES Le...

  8. The ocean quasi-homogeneous layer model and global cycle of carbon dioxide in system of atmosphere-ocean

    Science.gov (United States)

    Glushkov, Alexander; Glushkov, Alexander; Loboda, Nataliya; Khokhlov, Valery; Serbov, Nikoly; Svinarenko, Andrey

    The purpose of this paper is carrying out the detailed model of the CO2 global turnover in system of "atmosphere-ocean" with using the ocean quasi-homogeneous layer model. Practically all carried out models are functioning in the average annual regime and accounting for the carbon distribution in bio-sphere in most general form (Glushkov et al, 2003). We construct a modified model for cycle of the carbon dioxide, which allows to reproduce a season dynamics of carbon turnover in ocean with account of zone ocean structure (up quasi-homogeneous layer, thermocline and deepest layer). It is taken into account dependence of the CO2 transfer through the bounder between atmosphere and ocean upon temperature of water and air, wind velocity, buffer mechanism of the CO2 dissolution. The same program is realized for atmosphere part of whole system. It is obtained a tempo-ral and space distribution for concentration of non-organic carbon in ocean, partial press of dissolute CO2 and value of exchange on the border between atmosphere and ocean. It is estimated a role of the wind intermixing of the up ocean layer. The increasing of this effect leads to increasing the plankton mass and further particles, which are transferred by wind, contribute to more quick immersion of microscopic shells and organic material. It is fulfilled investigation of sen-sibility of the master differential equations system solutions from the model parameters. The master differential equa-tions system, describing a dynamics of the CO2 cycle, is numerically integrated by the four order Runge-Cutt method under given initial values of valuables till output of solution on periodic regime. At first it is indicated on possible real-zation of the chaos scenario in system. On our data, the difference of the average annual values for the non-organic car-bon concentration in the up quasi-homogeneous layer between equator and extreme southern zone is 0.15 mol/m3, be-tween the equator and extreme northern zone is 0

  9. Phase and amplitude of ecosystem carbon release and uptake potentials as derived from FLUXNET measurements

    DEFF Research Database (Denmark)

    Falge, E.; Tenhunen, J.; Baldocchi, D.

    2002-01-01

    , as well as for global inversion studies, and can help improve phenological modules in SVAT or biogeochemical models. The results of this study have important validation potential for global carbon cycle modeling. The phasing of respiratory and assimilatory capacity differed within forest types...... in four classes: (1) boreal and high altitude conifers and grasslands: (2) temperate deciduous and temperate conifers; (3) tundra and crops; (4) evergreen Mediterranean and tropical forest,,, Similar results are found for maximum daytime uptake (F-min) and the integral net carbon flux, but temperate......-min are largest for managed grasslands and crops. Largest observed values of F-min varied between -48 and -2 mumol m(-2) s(-1), decreasing in the order C-4-crops > C-3-crops > temperate deciduous forests > temperate conifers > boreal conifers > tundra ecosystems. Due to data restrictions, our analysis centered...

  10. Multi-Model Assessment of Trends and Variability in Terrestrial Carbon Uptake in India

    Science.gov (United States)

    Rao, A. S.; Bala, G.; Ravindranath, N. H.

    2015-12-01

    Indian terrestrial ecosystem exhibits large temporal and spatial variability in carbon sources and sinks due to its monsoon based climate system, diverse land use and land cover distribution and cultural practices. In this study, a multi-model based assessment is made to study the trends and variability in the land carbon uptake for India over the 20th century. Data from nine models which are a part of a recent land surface model intercomparison project called TRENDY is used for the study. These models are driven with common forcing data over the period of 1901-2010. Model output variables assessed include: gross primary production (GPP), heterotrophic respiration (Rh), autotrophic respiration (Ra) and net primary production (NPP). The net ecosystem productivity (NEP) for the Indian region was calculated as a difference of NPP and Rh and it was found that NEP for the region indicates an estimated increase in uptake over the century by -0.6 TgC/year per year. NPP for India also shows an increasing trend of 2.03% per decade from 1901-2010. Seasonal variation in the multimodel mean NPP is maximum during the southwest monsoon period (JJA) followed by the post monsoon period (SON) and is attributed to the maximum in rainfall for the region during the months of JJA. To attribute the changes seen in the land carbon variables, influence of climatic drivers such as precipitation, temperature and remote influences of large scale phenomenon such as ENSO on the land carbon of the region are also estimated in the study. It is found that although changes in precipitation shows a good correlation to the changes seen in NEP, remote drivers like ENSO do not have much effect on them. The Net Ecosystem Exchange is calculated with the inclusion of the land use change flux and fire flux from the models. NEE suggests that the region behaves as a small sink for carbon with an net uptake of 5 GtC over the past hundred years.

  11. Functional interaction between bicarbonate transporters and carbonic anhydrase modulates lactate uptake into mouse cardiomyocytes.

    Science.gov (United States)

    Peetz, Jan; Barros, L Felipe; San Martín, Alejandro; Becker, Holger M

    2015-07-01

    Blood-derived lactate is a precious energy substrate for the heart muscle. Lactate is transported into cardiomyocytes via monocarboxylate transporters (MCTs) together with H(+), which couples lactate uptake to cellular pH regulation. In this study, we have investigated how the interplay between different acid/base transporters and carbonic anhydrases (CA), which catalyze the reversible hydration of CO2, modulates the uptake of lactate into isolated mouse cardiomyocytes. Lactate transport was estimated both as lactate-induced acidification and as changes in intracellular lactate levels measured with a newly developed Förster resonance energy transfer (FRET) nanosensor. Recordings of intracellular pH showed an increase in the rate of lactate-induced acidification when CA was inhibited by 6-ethoxy-2-benzothiazolesulfonamide (EZA), while direct measurements of lactate flux demonstrated a decrease in MCT transport activity, when CA was inhibited. The data indicate that catalytic activity of extracellular CA increases lactate uptake and counteracts intracellular lactate-induced acidification. We propose a hypothetical model, in which HCO3 (-), formed from cell-derived CO2 at the outer surface of the cardiomyocyte plasma membrane by membrane-anchored, extracellular CA, is transported into the cell via Na(+)/HCO3 (-) cotransport to counteract intracellular acidification, while the remaining H(+) stabilizes extracellular pH at the surface of the plasma membrane during MCT activity to enhance lactate influx into cardiomyocytes.

  12. Seasonality and Interannual Variability of Carbon Uptake and Respiration in a California Oak Savanna

    Science.gov (United States)

    Ma, S.; Baldocchi, D.; Xu, L.

    2005-12-01

    Estimating terrestrial carbon sink with large-scale modeling research requires understanding the physiological and ecological processes associated with the carbon uptake and respiration of ecosystems and their variability in seasons and years. This study was conducted in an oak/grass savanna ecosystem in California, USA. The savanna ecosystem consists of blue oak trees ( Quercus douglasii) in the overstory and annual C3 grasses in the understory. Fluxes of CO2 were measured above the canopy (overstory) and the grasses (understory) from 2001 to 2005 with two eddy covariance systems. Under typical Mediterranean Climate, net ecosystem exchange of CO2 (NEE), ecosystem respiration (Reco), and gross primary production (GPP) in this savanna ecosystem had a distinctive dry-wet seasonal pattern. Leaf area index, leaf nitrogen concentration, and leaf carbon stable isotope discrimination reflected the responses of leaf to the seasonality and interannual variability. Light- use efficiency, the ratio of GPP to absorbed photosynthetically active radiation (aPAR), was not consistent within a year or from year to year, indicating that photosynthesis process was constrained with low temperature during the beginning of the wet season and limited by precipitation during the summer drought. Annual NEE, Reco, and GPP above the canopy varied significantly between years, varying from -108 - 133 gC m-2, 780 - 988 gC m-2, and 646 - 963 gC m-2, respectively. The difference of interannual Reco was 1.2 times of that of interannual GPP. There was a tight relationship between annual NEE and the precipitation during the period with daily mean temperature varying between 10 - 20°C, equivalent to precipitation during March and April. The longer the period lasted, the higher carbon uptake occurred. Estimated annual NEE from 1949 - 2005 in the savanna ecosystem varied between ~-400 - 200 gC m-2.

  13. BILP-19-An Ultramicroporous Organic Network with Exceptional Carbon Dioxide Uptake.

    Science.gov (United States)

    Klumpen, Christoph; Radakovitsch, Florian; Jess, Andreas; Senker, Jürgen

    2017-08-12

    Porous benzimidazole-based polymers (BILPs) have proven to be promising for carbon dioxide capture and storage. The polarity of their chemical structure in combination with an inherent porosity allows for adsorbing large amounts of carbon dioxide in combination with high selectivities over unpolar guest molecules such as methane and nitrogen. For this reason, among purely organic polymers, BILPs contain some of the most effective networks to date. Nevertheless, they are still outperformed by competitive materials such as metal-organic frameworks (MOFs) or metal doped porous polymers. Here, we report the synthesis of BILP-19 and its exceptional carbon dioxide uptake of up to 6 mmol•g-1 at 273 K, making the network comparable to state-of-the-art materials. BILP-19 precipitates in a particulate structure with a strongly anisotropic growth into platelets, indicating a sheet-like structure for the network. It exhibits only a small microporous but a remarkable ultra-microporous surface area of 144 m2•g-1 and 1325 m2•g-1, respectively. We attribute the exceptional uptake of small guest molecules such as carbon dioxide and water to the distinct ultra-microporosity. Additionally, a pronounced hysteresis for both guests is observed, which in combination with the platelet character is probably caused by an expansion of the interparticle space, creating additional accessible ultra-microporous pore volume. For nitrogen and methane, this effect does not occur which explains their low affinity. In consequence, Henry selectivities of 123 for CO2/N2 at 298 K and 12 for CO2/CH4 at 273 K were determined. The network was carefully characterized with solid-state nuclear magnetic resonance (NMR) and infrared (IR) spectroscopy, thermal gravimetry (TG) and elemental analyses as well as physisorption experiments with Ar, N2, CO2, CH4 and water.

  14. The impact of whaling on the ocean carbon cycle: why bigger was better.

    Directory of Open Access Journals (Sweden)

    Andrew J Pershing

    Full Text Available BACKGROUND: Humans have reduced the abundance of many large marine vertebrates, including whales, large fish, and sharks, to only a small percentage of their pre-exploitation levels. Industrial fishing and whaling also tended to preferentially harvest the largest species and largest individuals within a population. We consider the consequences of removing these animals on the ocean's ability to store carbon. METHODOLOGY/PRINCIPAL FINDINGS: Because body size is critical to our arguments, our analysis focuses on populations of baleen whales. Using reconstructions of pre-whaling and modern abundances, we consider the impact of whaling on the amount of carbon stored in living whales and on the amount of carbon exported to the deep sea by sinking whale carcasses. Populations of large baleen whales now store 9.1×10(6 tons less carbon than before whaling. Some of the lost storage has been offset by increases in smaller competitors; however, due to the relative metabolic efficiency of larger organisms, a shift toward smaller animals could decrease the total community biomass by 30% or more. Because of their large size and few predators, whales and other large marine vertebrates can efficiently export carbon from the surface waters to the deep sea. We estimate that rebuilding whale populations would remove 1.6×10(5 tons of carbon each year through sinking whale carcasses. CONCLUSIONS/SIGNIFICANCE: Even though fish and whales are only a small portion of the ocean's overall biomass, fishing and whaling have altered the ocean's ability to store and sequester carbon. Although these changes are small relative to the total ocean carbon sink, rebuilding populations of fish and whales would be comparable to other carbon management schemes, including ocean iron fertilization.

  15. Weakening temperature control on the interannual variations of spring carbon uptake across northern lands

    Energy Technology Data Exchange (ETDEWEB)

    Piao, Shilong [Chinese Academy of Sciences (CAS), Beijing (China); Peking Univ., Beijing (China); Liu, Zhuo [Peking Univ., Beijing (China); Wang, Tao [Chinese Academy of Sciences (CAS), Beijing (China); Peng, Shushi [Peking Univ., Beijing (China); Ciais, Philippe [Alternative Energies and Atomic Energy Commission (CEA), Gif-sur-Yvette (France); Huang, Mengtian [Peking Univ., Beijing (China); Ahlstrom, Anders [Stanford Univ., CA (United States); Burkhart, John F. [Univ. of Oslo (Norway); Chevallier, Frédéric [Alternative Energies and Atomic Energy Commission (CEA), Gif-sur-Yvette (France); Janssens, Ivan A. [Univ. of Antwerp, Wilrijk (Belgium); Jeong, Su-Jong [South Univ. of Science and Technology of China, Shenzhen (China); Lin, Xin [Alternative Energies and Atomic Energy Commission (CEA), Gif-sur-Yvette (France); Mao, Jiafu [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Miller, John [National Oceanic and Atmospheric Administration Earth Systems Research Lab., Boulder, CO (United States); Univ. of Colorado, Boulder, CO (United States); Mohammat, Anwar [Chinese Academy of Sciences (CAS), Beijing (China); Myneni, Ranga B. [Boston Univ., MA (United States); Peñuelas, Josep [Centre for Ecological Research and Forestry Applications (CREAF), Barcelona (Spain); Shi, Xiaoying [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Stohl, Andreas [Norwegian Institute for Air Research (NILU), Kjeller (Norway); Yao, Yitong [Peking Univ., Beijing (China); Zhu, Zaichun [Peking Univ., Beijing (China); Tans, Pieter P. [National Oceanic and Atmospheric Administration Earth Systems Research Lab., Boulder, CO (United States)

    2017-04-24

    Ongoing spring warming allows the growing season to begin earlier, enhancing carbon uptake in northern ecosystems. We use 34 years of atmospheric CO2 concentration measurements at Barrow, Alaska (BRW, 71° N) to show that the interannual relationship between spring temperature and carbon uptake has recently shifted. Here, we use two indicators: the spring zero-crossing date of atmospheric CO2 (SZC) and the magnitude of CO2 drawdown between May and June (SCC). The previously reported strong correlation between SZC, SCC and spring land temperature (ST) was found in the first 17 years of measurements, but disappeared in the last 17 years. As a result, the sensitivity of both SZC and SCC to warming decreased. Simulations with an atmospheric transport model coupled to a terrestrial ecosystem model suggest that the weakened interannual correlation of SZC and SCC with ST in the last 17 years is attributable to the declining temperature response of spring net primary productivity (NPP) rather than to changes in heterotrophic respiration or in atmospheric transport patterns. Reduced chilling during dormancy and emerging light limitation are possible mechanisms that may have contributed to the loss of NPP response to ST. These results thus challenge the ‘warmer spring–bigger sink’ mechanism.

  16. The chest X-ray in pulmonary capillary haemorrhage: correlation with carbon monoxide uptake

    International Nuclear Information System (INIS)

    Bowley, N.B.; Hughes, J.M.B.; Steiner, R.E.

    1979-01-01

    Serial changes in carbon monoxide uptake (Ksub(CO) or Dsub(L)CO/VA) were used to monitor episodes of pulmonary capillary haemorrhage in Goodpasture's syndrome (13 cases), immune complex nephritis (three cases) and idiopathic haemosiderosis (one case). Air-space shadowing on the chest X-ray (on a scoring system 0 to 12) was assessed in the light of the changes of Ksub(CO). In 14 out of 27 episodes of bleeding, the rise and fall of Ksub(CO) was matched in time by the appearance and disappearance of air-space shadowing on the chest X-ray. In six episodes the chest X-ray remained normal despite a rise of Ksub(CO). In two cases air-space shadowing appeared up to 48 h after the rise of Ksub(CO). On five occasions chest X-ray abnormalities preceded the rise of Ksub(CO) but chest infection or fluid overload accounted for three of these. In cases with suspected pulmonary capillary haemorrhage, measurements of carbon monoxide uptake will provide additional information and will assist in the interpretation of the chest X-ray. (author)

  17. Southern Ocean biogeochemical control of glacial/interglacial carbon dioxide change

    Science.gov (United States)

    Sigman, D. M.

    2014-12-01

    In the effort to explain the lower atmospheric CO2 concentrations observed during ice ages, two of the first hypotheses involved redistributing dissolved inorganic carbon (DIC) within the ocean. Broecker (1982) proposed a strengthening of the ocean's biological pump during ice ages, which increased the dissolved inorganic carbon gradient between the dark, voluminous ocean interior and the surface ocean's sun-lit, wind-mixed layer. Boyle (1988) proposed a deepening in the ocean interior's pool of DIC associated with organic carbon regeneration, with its concentration maximum shifting from intermediate to abyssal depths. While not irrefutable, evidence has arisen that these mechanisms can explain much of the ice age CO2 reduction and that both were activated by changes in the Southern Ocean. In the Antarctic Zone, reduced exchange of water between the surface and the underlying ocean sequestered more DIC in the ocean interior (the biological pump mechanism). Dust-borne iron fertilization of the Subantarctic surface lowered CO2 partly by the biological pump mechanism and partly by Boyle's carbon deepening. Each mechanism owes a part of its CO2 effect to a transient increase in seafloor calcium carbonate dissolution, which raised the ice age ocean's alkalinity, causing it to absorb more CO2. However, calcium carbonate cycling also sets limits on these mechanisms and their CO2 effects, such that the combination of Antarctic and Subantarctic changes is needed to achieve the full (80-100 ppm) ice age CO2 decline. Data suggest that these changes began at different phases in the development of the last ice age, 110 and 70 ka, respectively, explaining a 40 ppm CO2 drop at each time. We lack a robust understanding of the potential causes for both the implied reduction in Antarctic surface/deep exchange and the increase in Subantarctic dust supply during ice ages. Thus, even if the evidence for these Southern Ocean changes were to become incontrovertible, conceptual gaps stand

  18. Observations of the uptake of carbonyl sulfide (COS by trees under elevated atmospheric carbon dioxide concentrations

    Directory of Open Access Journals (Sweden)

    L. Sandoval-Soto

    2012-08-01

    Full Text Available Global change forces ecosystems to adapt to elevated atmospheric concentrations of carbon dioxide (CO2. We understand that carbonyl sulfide (COS, a trace gas which is involved in building up the stratospheric sulfate aerosol layer, is taken up by vegetation with the same triad of the enzymes which are metabolizing CO2, i.e. ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco, phosphoenolpyruvate carboxylase (PEP-Co and carbonic anhydrase (CA. Therefore, we discuss a physiological/biochemical acclimation of these enzymes affecting the sink strength of vegetation for COS. We investigated the acclimation of two European tree species, Fagus sylvatica and Quercus ilex, grown inside chambers under elevated CO2, and determined the exchange characteristics and the content of CA after a 1–2 yr period of acclimation from 350 ppm to 800 ppm CO2. We demonstrate that a compensation point, by definition, does not exist. Instead, we propose to discuss a point of uptake affinity (PUA. The results indicate that such a PUA, the CA activity and the deposition velocities may change and may cause a decrease of the COS uptake by plant ecosystems, at least as long as the enzyme acclimation to CO2 is not surpassed by an increase of atmospheric COS. As a consequence, the atmospheric COS level may rise causing an increase of the radiative forcing in the troposphere. However, this increase is counterbalanced by the stronger input of this trace gas into the stratosphere causing a stronger energy reflection by the stratospheric sulfur aerosol into space (Brühl et al., 2012. These data are very preliminary but may trigger a discussion on COS uptake acclimation to foster measurements with modern analytical instruments.

  19. The global distribution of leaf chlorophyll content and seasonal controls on carbon uptake

    Science.gov (United States)

    Croft, H.; Chen, J. M.; Luo, X.; Bartlett, P. A.; Staebler, R. M.; He, L.; Mo, G.; Luo, S.; Simic, A.; Arabian, J.; He, Y.; Zhang, Y.; Beringer, J.; Hutley, L. B.; Noland, T. L.; Arellano, P.; Stahl, C.; Homolová, L.; Bonal, D.; Malenovský, Z.; Yi, Q.; Amiri, R.

    2017-12-01

    Leaf chlorophyll (ChlLeaf) is crucial to biosphere-atmosphere exchanges of carbon and water, and the functioning of terrestrial ecosystems. Improving the accuracy of modelled photosynthetic carbon uptake is a central priority for understanding ecosystem response to a changing climate. A source of uncertainty within gross primary productivity (GPP) estimates is the failure to explicitly consider seasonal controls on leaf photosynthetic potential. Whilst the inclusion of ChlLeafinto carbon models has shown potential to provide a physiological constraint, progress has been hampered by the absence of a spatially-gridded, global chlorophyll product. Here, we present the first spatially-continuous, global view of terrestrial ChlLeaf, at weekly intervals. Satellite-derived ChlLeaf was modelled using a physically-based radiative transfer modelling approach, with a two stage model inversion method. 4-Scale and SAIL canopy models were first used to model leaf-level reflectance from ENIVSAT MERIS 300m satellite data. The PROSPECT leaf model was then used to derive ChlLeaf from the modelled leaf reflectance. This algorithm was validated using measured ChlLeaf data from 248 measurements within 26 field locations, covering six plant functional types (PFTs). Modelled results show very good relationships with measured data, particularly for deciduous broadleaf forests (R2 = 0.67; pmake an important step towards improving the accuracy of global carbon budgets.

  20. Carbonate dissolution in the South Atlantic Ocean: evidence from ultrastructure breakdown in Globigerina bulloides

    Science.gov (United States)

    Dittert, Nicolas; Henrich, Rüdiger

    2000-04-01

    Ultrastructure dissolution susceptibility of the planktic foraminifer Globigerina bulloides, carbonate ion content of the water column, calcium carbonate content of the sediment surface, and carbonate/carbon weight percentage ratio derived from sediment surface samples were investigated in order to reconstruct the position of the calcite saturation horizon, the sedimentary calcite lysocline, and the calcium carbonate compensation depth (CCD) in the modern South Atlantic Ocean. Carbonate ion data from the water column refer to the GEOSECS locations 48, 103, and 109 and calcium carbonate data come from 19 GeoB sediment surface samples of 4 transects into the Brazil, the Guinea, and the Cape Basins. We present a new (paleo-) oceanographic tool, namely the Globigerina bulloides dissolution index (BDX). Further, we give evidence (a) for progressive G. bulloides ultrastructural breakdown with increasing carbonate dissolution even above the lysocline; (b) for a sharp BDX increase at the sedimentary lysocline; and (c) for the total absence of this species at the CCD. BDX puts us in the position to distinguish the upper open ocean and the upwelling influenced continental margin above from the deep ocean below the sedimentary lysocline. Carbonate ion data from water column samples, calcite weight percentage data from surface sediment samples, and carbonate/carbon weight percentage ratio appear to be good proxies to confirm BDX. As shown by BDX both the calcite saturation horizon (in the water column) and the sedimentary lysocline (at the sediment-water interface) mark the boundary between the carbonate ion undersaturated and highly corrosive Antarctic Bottom Water and the carbonate ion saturated North Atlantic Deep Water (NADW) of the modern South Atlantic.

  1. Climate Change Impacts on the Organic Carbon Cycle at the Land-Ocean Interface

    Science.gov (United States)

    Canuel, Elizabeth A.; Cammer, Sarah S.; McIntosh, Hadley A.; Pondell, Christina R.

    2012-05-01

    Estuaries are among the most altered and vulnerable marine ecosystems. These ecosystems will likely continue to deteriorate owing to increased population growth in coastal regions, expected temperature and precipitation changes associated with climate change, and their interaction with each other, leading to serious consequences for the ecological and societal services they provide. A key function of estuaries is the transfer, transformation, and burial of carbon and other biogenic elements exchanged between the land and ocean systems. Climate change has the potential to influence the carbon cycle through anticipated changes to organic matter production in estuaries and through the alteration of carbon transformation and export processes. This review discusses the effects of climate change on processes influencing the cycling of organic carbon in estuaries, including examples from three temperate estuaries in North America. Our goal is to evaluate the impact of climate change on the connectivity of terrestrial, estuarine, and coastal ocean carbon cycles.

  2. Combined simulation of carbon and water isotopes in a global ocean model

    Science.gov (United States)

    Paul, André; Krandick, Annegret; Gebbie, Jake; Marchal, Olivier; Dutkiewicz, Stephanie; Losch, Martin; Kurahashi-Nakamura, Takasumi; Tharammal, Thejna

    2013-04-01

    Carbon and water isotopes are included as passive tracers in the MIT general circulation model (MITgcm). The implementation of the carbon isotopes is based on the existing MITgcm carbon cycle component and involves the fractionation processes during photosynthesis and air-sea gas exchange. Special care is given to the use of a real freshwater flux boundary condition in conjunction with the nonlinear free surface of the ocean model. The isotopic content of precipitation and water vapor is obtained from an atmospheric GCM (the NCAR CAM3) and mapped onto the MITgcm grid system, but the kinetic fractionation during evaporation is treated explicitly in the ocean model. In a number of simulations, we test the sensitivity of the carbon isotope distributions to the formulation of fractionation during photosynthesis and compare the results to modern observations of δ13C and Δ14C from GEOSECS, WOCE and CLIVAR. Similarly, we compare the resulting distribution of oxygen isotopes to modern δ18O data from the NASA GISS Global Seawater Oxygen-18 Database. The overall agreement is good, but there are discrepancies in the carbon isotope composition of the surface water and the oxygen isotope composition of the intermediate and deep waters. The combined simulation of carbon and water isotopes in a global ocean model will provide a framework for studying present and past states of ocean circulation such as postulated from deep-sea sediment records.

  3. Climate change impact on future ocean acidification

    International Nuclear Information System (INIS)

    McNeil, Ben

    2007-01-01

    Full text: Elevated atmospheric C02 levels and associated uptake by the ocean is changing its carbon chemistry, leading to an acidification. The implications of future ocean acidification on the marine ecosystem are unclear but seemingly detrimental particularly to those organisms and phytoplankton that secrete calcium carbonate (like corals). Here we present new results from the Australian CSIRO General Circulation Model that predicts the changing nature of oceanic carbon chemistry in response to future climate change feedbacks (circulation, temperature and biological). We will discuss the implications of future ocean acidification and the potential implications on Australia's marine ecosystems

  4. Innovative nanoporous carbons with ultrahigh uptakes for capture and reversible storage of CO{sub 2} and volatile iodine

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Hanxue; La, Peiqing [College of Petrochemical Technology, Lanzhou University of Technology, Langongping Road 287, Lanzhou 730050, PR China (China); Yang, Ruixia [State Key Laboratory of Molecular Reaction Dynamics, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023 (China); Zhu, Zhaoqi; Liang, Weidong; Yang, Baoping [College of Petrochemical Technology, Lanzhou University of Technology, Langongping Road 287, Lanzhou 730050, PR China (China); Li, An, E-mail: lian2010@lut.cn [College of Petrochemical Technology, Lanzhou University of Technology, Langongping Road 287, Lanzhou 730050, PR China (China); Deng, Weiqiao, E-mail: dengwq@dicp.ac.cn [State Key Laboratory of Molecular Reaction Dynamics, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023 (China)

    2017-01-05

    Highlights: • Cigarette filter was utilized to prepare highly porous carbons as super absorbents. • The porous carbons exhibit excellent iodine uptake. • The porous carbons show high CO{sub 2} adsorption capacity of 6.0 mmol g{sup −1} at 273 K. - Abstract: Porous carbons as solid-state adsorbents have recently attracted considerable interest in the areas of storage and capture of CO{sub 2} as well as the adsorption of radioactive matters. In this work, cigarette butts, one kind of common wastes referring to the filters, were utilized to prepare highly porous carbons by KOH activation in argon atmosphere. The resulting porous carbon shows a high specific surface area of up to 2751 m{sup 2} g{sup −1} with abundant micropores. The resulting porous carbon exhibits excellent iodine uptake of 262 wt% and high CO{sub 2} adsorption capacity of 6.0 mmol g{sup −1} at ambient pressure and 273 K, which both are among the highest values reported to date. Given these excellent iodine uptake, CO{sub 2} adsorption capacity, ease of preparation as well as good physiochemical stability, the porous carbons derived from cigarette butts show great potential in the reversible adsorption of radioactive iodine and CO{sub 2}.

  5. Shallow Carbon Export from an Iron fertilised Plankton Bloom in the Southern Ocean

    Science.gov (United States)

    Sanders, R.; Pollard, R.; Morris, P.; Statham, P.; Moore, C. M. M.; Lucas, M.

    2009-04-01

    Some regions of the global ocean, notably the Southern Ocean, have high levels of macronutrients yet low levels of chlorophyll (the high nutrient, low chlorophyll or HNLC condition). Numerous artificial iron fertilization experiments conducted in the Southern Ocean have resulted in enhanced phytoplankton biomass and macronutrient drawdown. However the subsequent long-term biogeochemical consequences of such iron fertilization are unclear due in part to the limited size and duration of such experiments. An alternative way to assess the affect of iron over the Southern Ocean biological carbon pump is to observe the evolution of plankton production in regions of the Southern Ocean where shallow topography and Ocean currents interact to promote to release terrestrial iron into HNLC waters. During 2004-5 RRS Discovery conduced a complex programme of observations in such a region around the Crozet Islands in the SW Indian Ocean. The results of this programme, focussing on a quantitative estimate of carbon export per unit iron addition, will be presented.

  6. Challenges for present and future estimates of anthropogenic carbon in the Indian Ocean

    Science.gov (United States)

    Goyet, C.; Touratier, F.

    One of the main challenges we face today is to determine the evolution of the penetration of anthropogenic CO2 into the Indian Ocean and its impacts on marine and human life. Anthropogenic CO2 reaches the ocean via air-sea interactions as well as riverine inputs. It is then stored in the ocean and follows the oceanic circulation. As the carbon dioxide from the atmosphere penetrates into the sea, it reacts with water and acidifies the ocean. Consequently, the whole marine ecosystem is perturbed, thus potentially affecting the food web, which has, in turn, a direct impact on seafood supply for humans. Naturally, this will mainly affect the growing number of people living in coastal areas. Although anthropogenic CO2 in the ocean is identical with natural CO2 and therefore cannot be detected alone, many approaches are available today to estimate it. Since most of the results of these methods are globally in agreement, here we chose one of these methods, the tracer using oxygen, total inorganic carbon, and total alkalinity (TrOCA) approach, to compute the 3-D distribution of the anthropogenic CO2 concentrations throughout the Indian Ocean. The results of this distribution clearly illustrate the contrast between the Arabian Sea and the Bay of Bengal. They further show the importance of the southern part of this ocean that carries some anthropogenic CO2 at great depths. In order to determine the future anthropogenic impacts on the Indian Ocean, it is urgent and necessary to understand the present state. As the seawater temperature increases, how and how fast will the ocean circulation change? What will the impacts on seawater properties be? Many people are living on the bordering coasts, how will they be affected?

  7. High rates of microbial carbon turnover in sediments in the deepest oceanic trench on Earth

    DEFF Research Database (Denmark)

    Glud, Ronnie N.; Wenzhoefer, Frank; Middelboe, Mathias

    2013-01-01

    Microbes control the decomposition of organic matter in marine sediments. Decomposition, in turn, contributes to oceanic nutrient regeneration and influences the preservation of organic carbon(1). Generally, rates of benthic decomposition decline with increasing water depth, although given the vast...... extent of the abyss, deep-sea sediments are quantitatively important for the global carbon cycle(2,3). However, the deepest regions of the ocean have remained virtually unexplored(4). Here, we present observations of microbial activity in sediments at Challenger Deep in the Mariana Trench in the central...

  8. Ozone uptake, water loss and carbon exchange dynamics in annually drought-stressed Pinus ponderosa forests: measured trends and parameters for uptake modeling.

    Science.gov (United States)

    Panek, Jeanne A

    2004-03-01

    This paper describes 3 years of physiological measurements on ponderosa pine (Pinus ponderosa Dougl. ex Laws.) growing along an ozone concentration gradient in the Sierra Nevada, California, including variables necessary to parameterize, validate and modify photosynthesis and stomatal conductance algorithms used to estimate ozone uptake. At all sites, gas exchange was under tight stomatal control during the growing season. Stomatal conductance was strongly correlated with leaf water potential (R2=0.82), which decreased over the growing season with decreasing soil water content (R2=0.60). Ozone uptake, carbon uptake, and transpirational water loss closely followed the dynamics of stomatal conductance. Peak ozone and CO2 uptake occurred in early summer and declined progressively thereafter. As a result, periods of maximum ozone uptake did not correspond to periods of peak ozone concentration, underscoring the inappropriateness of using current metrics based on concentration (e.g., SUM0, W126 and AOT40) for assessing ozone exposure risk to plants in this climate region. Both Jmax (maximum CO2-saturated photosynthetic rate, limited by electron transport) and Vcmax (maximum rate of Rubisco-limited carboxylation) increased toward the middle of the growing season, then decreased in September. Intrinsic water-use efficiency rose with increasing drought stress, as expected. The ratio of Jmax to Vcmax was similar to literature values of 2.0. Nighttime respiration followed a Q10 of 2.0, but was significantly higher at the high-ozone site. Respiration rates decreased by the end of the summer as a result of decreased metabolic activity and carbon stores.

  9. Strong constraint on modelled global carbon uptake using solar-induced chlorophyll fluorescence data.

    Science.gov (United States)

    MacBean, Natasha; Maignan, Fabienne; Bacour, Cédric; Lewis, Philip; Peylin, Philippe; Guanter, Luis; Köhler, Philipp; Gómez-Dans, Jose; Disney, Mathias

    2018-01-31

    Accurate terrestrial biosphere model (TBM) simulations of gross carbon uptake (gross primary productivity - GPP) are essential for reliable future terrestrial carbon sink projections. However, uncertainties in TBM GPP estimates remain. Newly-available satellite-derived sun-induced chlorophyll fluorescence (SIF) data offer a promising direction for addressing this issue by constraining regional-to-global scale modelled GPP. Here, we use monthly 0.5° GOME-2 SIF data from 2007 to 2011 to optimise GPP parameters of the ORCHIDEE TBM. The optimisation reduces GPP magnitude across all vegetation types except C4 plants. Global mean annual GPP therefore decreases from 194 ± 57 PgCyr -1 to 166 ± 10 PgCyr -1 , bringing the model more in line with an up-scaled flux tower estimate of 133 PgCyr -1 . Strongest reductions in GPP are seen in boreal forests: the result is a shift in global GPP distribution, with a ~50% increase in the tropical to boreal productivity ratio. The optimisation resulted in a greater reduction in GPP than similar ORCHIDEE parameter optimisation studies using satellite-derived NDVI from MODIS and eddy covariance measurements of net CO 2 fluxes from the FLUXNET network. Our study shows that SIF data will be instrumental in constraining TBM GPP estimates, with a consequent improvement in global carbon cycle projections.

  10. Stirring Up the Biological Pump: Vertical Mixing and Carbon Export in the Southern Ocean

    Science.gov (United States)

    Stukel, Michael R.; Ducklow, Hugh W.

    2017-09-01

    The biological carbon pump (BCP) transports organic carbon from the surface to the ocean's interior via sinking particles, vertically migrating organisms, and passive transport of organic matter by advection and diffusion. While many studies have quantified sinking particles, the magnitude of passive transport remains poorly constrained. In the Southern Ocean weak thermal stratification, strong vertical gradients in particulate organic matter, and weak vertical nitrate gradients suggest that passive transport from the euphotic zone may be particularly important. We compile data from seasonal time series at a coastal site near Palmer Station, annual regional cruises in the Western Antarctic Peninsula (WAP), cruises throughout the broader Southern Ocean, and SOCCOM (Southern Ocean Carbon and Climate Observations and Modeling) autonomous profiling floats to estimate spatial and temporal patterns in vertical gradients of nitrate, particulate nitrogen (PN), and dissolved organic carbon. Under a steady state approximation, the ratio of ∂PN/∂z to ∂NO3-/∂z suggests that passive transport of PN may be responsible for removing 46% (37%-58%) of the nitrate introduced into the surface ocean of the WAP (with dissolved organic matter contributing an additional 3-6%) and for 23% (19%-28%) of the BCP in the broader Southern Ocean. A simple model parameterized with in situ nitrate, PN, and primary production data suggested that passive transport was responsible for 54% of the magnitude of the BCP in the WAP. Our results highlight the potential importance of passive transport (by advection and diffusion) of organic matter in the Southern Ocean but should only be considered indicative of high passive transport (rather than conclusive evidence) due to our steady state assumptions.

  11. Development of improved space sampling strategies for ocean chemical properties: Total carbon dioxide and dissolved nitrate

    Science.gov (United States)

    Goyet, Catherine; Davis, Daniel; Peltzer, Edward T.; Brewer, Peter G.

    1995-01-01

    Large-scale ocean observing programs such as the Joint Global Ocean Flux Study (JGOFS) and the World Ocean Circulation Experiment (WOCE) today, must face the problem of designing an adequate sampling strategy. For ocean chemical variables, the goals and observing technologies are quite different from ocean physical variables (temperature, salinity, pressure). We have recently acquired data on the ocean CO2 properties on WOCE cruises P16c and P17c that are sufficiently dense to test for sampling redundancy. We use linear and quadratic interpolation methods on the sampled field to investigate what is the minimum number of samples required to define the deep ocean total inorganic carbon (TCO2) field within the limits of experimental accuracy (+/- 4 micromol/kg). Within the limits of current measurements, these lines were oversampled in the deep ocean. Should the precision of the measurement be improved, then a denser sampling pattern may be desirable in the future. This approach rationalizes the efficient use of resources for field work and for estimating gridded (TCO2) fields needed to constrain geochemical models.

  12. Nutrient limitation reduces land carbon uptake in simulations with a model of combined carbon, nitrogen and phosphorus cycling

    Directory of Open Access Journals (Sweden)

    D. S. Goll

    2012-09-01

    Full Text Available Terrestrial carbon (C cycle models applied for climate projections simulate a strong increase in net primary productivity (NPP due to elevated atmospheric CO2 concentration during the 21st century. These models usually neglect the limited availability of nitrogen (N and phosphorus (P, nutrients that commonly limit plant growth and soil carbon turnover. To investigate how the projected C sequestration is altered when stoichiometric constraints on C cycling are considered, we incorporated a P cycle into the land surface model JSBACH (Jena Scheme for Biosphere–Atmosphere Coupling in Hamburg, which already includes representations of coupled C and N cycles.

    The model reveals a distinct geographic pattern of P and N limitation. Under the SRES (Special Report on Emissions Scenarios A1B scenario, the accumulated land C uptake between 1860 and 2100 is 13% (particularly at high latitudes and 16% (particularly at low latitudes lower in simulations with N and P cycling, respectively, than in simulations without nutrient cycles. The combined effect of both nutrients reduces land C uptake by 25% compared to simulations without N or P cycling. Nutrient limitation in general may be biased by the model simplicity, but the ranking of limitations is robust against the parameterization and the inflexibility of stoichiometry. After 2100, increased temperature and high CO2 concentration cause a shift from N to P limitation at high latitudes, while nutrient limitation in the tropics declines. The increase in P limitation at high-latitudes is induced by a strong increase in NPP and the low P sorption capacity of soils, while a decline in tropical NPP due to high autotrophic respiration rates alleviates N and P limitations. The quantification of P limitation remains challenging. The poorly constrained processes of soil P sorption and biochemical mineralization are identified as the main uncertainties in the strength of P limitation

  13. Uptake of Single-Walled Carbon Nanotubes Conjugated with DNA by Microvascular Endothelial Cells

    Directory of Open Access Journals (Sweden)

    Joseph Harvey

    2012-01-01

    Full Text Available Single-walled carbon nanotubes (SWCNTs have been proposed to have great therapeutic potential. SWCNTs conjugated with drugs or genes travel in the systemic circulation to reach target cells or tissues following extravasation from microvessels although the interaction between SWCNT conjugates and the microvascular endothelial cells (ECs remains unknown. We hypothesized that SWCNT-DNA conjugates would be taken up by microvascular ECs and that this process would be facilitated by SWCNTs compared to facilitation by DNA alone. ECs were treated with various concentrations of SWCNT-DNA-FITC conjugates, and the uptake and intracellular distribution of these conjugates were determined by a confocal microscope imaging system followed by quantitative analysis of fluorescence intensity. The uptake of SWCNT-DNA-FITC conjugates (2 μg/mL by microvascular ECs was significantly greater than that of DNA-FITC (2 μg/mL, observed at 6 hrs after treatment. For the intracellular distribution, SWCNT-DNA-FITC conjugates were detected in the nucleus of ECs, while DNA-FITC was restricted to the cytoplasm. The fluorescence intensity and distribution of SWCNTs were concentration and time independent. The findings demonstrate that SWCNTs facilitate DNA delivery into microvascular ECs, thus suggesting that SWCNTs serving as drug and gene vehicles have therapeutic potential.

  14. Uptake of radiocarbon from plant rhizosphere based on geological disposal of TRU waste. Root-uptake of radiocarbon carbon derived from acetic acid

    International Nuclear Information System (INIS)

    Ogiyama, Shinichi; Takeda, Hiroshi; Uchida, Shigeo; Suzuki, Hiroyuki; Inubushi, Kazuyuki

    2008-01-01

    Hydroponic experiments were conducted to examine root-uptake of 14 C in the form of acetic acid by 3 kinds of plants (marigold, tall fescue, and paddy rice) based on buried transuranic (TRU) waste disposal. Also, chamber experiment was conducted to examine loss of 14 C as vaporized carbon dioxide (CO 2 ) from the experimental tessera (spatially heterogeneous environment). The distribution of radioactivity in the plant, mediums, and carbon dioxide ( 14 CO 2 ) in the chamber were determined, and the distribution of 14 C in the plant was visualized by the autoradiography. The plants absorbed and assimilated 14 C through the roots. The amount of 14 C in marigold and tall fescue were higher than that of paddy rice. However, the amounts of 14 C-acetic acid absorbed by all the plants through their roots were considered to be very small. More so, 14 CO 2 gas was released from the culture solution to the atmosphere; however, it was not enough for the plant to perform photosynthesis. Assimilation of 14 C in the plant shoots would be because of 14 C movement of inorganic forms such as CO 2 and HCO 3 - via the roots. Thus, the results indicated that the plants absorbed 14 C through the roots and assimilated it into the shoots or edible parts not because of uptake of 14 C-acetic acid but because of uptake of 14 C in inorganic forms. (author)

  15. Climate change in the sea: the implications of increasing the carbon dioxide inputs to the surface ocean

    Energy Technology Data Exchange (ETDEWEB)

    Pfister, Cathy [University of Chicago

    2012-12-23

    The oceans are estimated to be absorbing one-third of the fossil fuel carbon released into the atmosphere, a process that is expected to change ocean carbon chemistry. I will present data from the Washington coast showing ocean pH declines and changes to the shell chemistry of bivalves. I will discuss implications of carbon cycle changes for marine species, including insights from a coastal area where I have worked for more than 24 years. I will summarize what we know to date about this process of “ocean acidification”.

  16. Simulated 21st century's increase in oceanic suboxia by CO2-enhanced biotic carbon export

    Science.gov (United States)

    Oschlies, Andreas; Schulz, Kai G.; Riebesell, Ulf; Schmittner, Andreas

    2008-12-01

    The primary impacts of anthropogenic CO2 emissions on marine biogeochemical cycles predicted so far include ocean acidification, global warming induced shifts in biogeographical provinces, and a possible negative feedback on atmospheric CO2 levels by CO2-fertilized biological production. Here we report a new potentially significant impact on the oxygen-minimum zones of the tropical oceans. Using a model of global climate, ocean circulation, and biogeochemical cycling, we extrapolate mesocosm-derived experimental findings of a pCO2-sensitive increase in biotic carbon-to-nitrogen drawdown to the global ocean. For a simulation run from the onset of the industrial revolution until A.D. 2100 under a "business-as-usual" scenario for anthropogenic CO2 emissions, our model predicts a negative feedback on atmospheric CO2 levels, which amounts to 34 Gt C by the end of this century. While this represents a small alteration of the anthropogenic perturbation of the carbon cycle, the model results reveal a dramatic 50% increase in the suboxic water volume by the end of this century in response to the respiration of excess organic carbon formed at higher CO2 levels. This is a significant expansion of the marine "dead zones" with severe implications not only for all higher life forms but also for oxygen-sensitive nutrient recycling and, hence, for oceanic nutrient inventories.

  17. Deglacial Millennial-scale Calcium Carbonate Spikes in the North Pacific Ocean

    Science.gov (United States)

    Chikamoto, M. O.; Timmermann, A.; Harada, N.; Okazaki, Y.

    2015-12-01

    Numerous paleoproxy records from the subarctic Pacific Ocean show two very pronounced deglacial peaks in calcium carbonate content for the Heinrich 1/ Bolling-Allerod (H1-BA) transition (at 14 ka) and for the Younger Dryas/Preboreal transition (at 11 ka). Focusing on the H1-BA transition, some model simulations capture the North Pacific shift from ventilated to stratified conditions and from cooling to warming conditions via oceanic and atmospheric connections between Atlantic and Pacific Oceans. To test the impact of these physical scenarios (variations in ocean stratification and temperature during the H1-BA transition) on calcite production or preservation, we conduct a series of idealized experiments using the Earth System Model Intermediate Complexity LOVECLIM. The variations in North Pacific Ocean stratification by anomalous freshwater forcing show low calcite productivity in associated with the subsurface nutrient decline. On the other hand, the rapid H1-BA warming of the North Pacific Ocean induced by anomalous heat forcing in turn increases calcite productivity due to the temperature-dependent growth rate of phytoplankton. These results suggest the possibility that the millennial-scale calcium carbonate peaks are the result of surface biogeochemical responses to the climate transition, not by the deep circulation response.

  18. Water masses as a unifying framework for understanding the Southern Ocean Carbon Cycle

    Directory of Open Access Journals (Sweden)

    D. Iudicone

    2011-05-01

    Full Text Available The scientific motivation for this study is to understand the processes in the ocean interior controlling carbon transfer across 30° S. To address this, we have developed a unified framework for understanding the interplay between physical drivers such as buoyancy fluxes and ocean mixing, and carbon-specific processes such as biology, gas exchange and carbon mixing. Given the importance of density in determining the ocean interior structure and circulation, the framework is one that is organized by density and water masses, and it makes combined use of Eulerian and Lagrangian diagnostics. This is achieved through application to a global ice-ocean circulation model and an ocean biogeochemistry model, with both components being part of the widely-used IPSL coupled ocean/atmosphere/carbon cycle model.

    Our main new result is the dominance of the overturning circulation (identified by water masses in setting the vertical distribution of carbon transport from the Southern Ocean towards the global ocean. A net contrast emerges between the role of Subantarctic Mode Water (SAMW, associated with large northward transport and ingassing, and Antarctic Intermediate Water (AAIW, associated with a much smaller export and outgassing. The differences in their export rate reflects differences in their water mass formation processes. For SAMW, two-thirds of the surface waters are provided as a result of the densification of thermocline water (TW, and upon densification this water carries with it a substantial diapycnal flux of dissolved inorganic carbon (DIC. For AAIW, principal formatin processes include buoyancy forcing and mixing, with these serving to lighten CDW. An additional important formation pathway of AAIW is through the effect of interior processing (mixing, including cabelling that serve to densify SAMW.

    A quantitative evaluation of the contribution of mixing, biology and gas exchange to the DIC evolution per water mass reveals that

  19. Response to Comment on "Dilution limits dissolved organic carbon utilization in the deep ocean"

    KAUST Repository

    Arrieta, Jesus

    2015-12-18

    Our recent finding that dilution limits dissolved organic carbon (DOC) utilization in the deep ocean has been criticized based on the common misconception that lability equates to rapid and complete utilization. Even when considering the redefinition of recalcitrant DOC recently proposed by Jiao et al., the dilution hypothesis best explains our experimental observations.

  20. Effects of ocean acidification on pelagic carbon fluxes in a mesocosm experiment

    NARCIS (Netherlands)

    Spilling, K.; Schulz, K.G.; Paul, A.J.; Boxhammer, T.; Achterberg, E.P.; Hornick, T.; Lischka, S.; Stuhr, A.; Bermúdez, R.; Czerny, J.; Crawfurd, K.; Brussaard, C.P.D.; Grossart, H.-P.; Riebesell, U.

    2016-01-01

    About a quarter of anthropogenic CO2 emissions are currently taken up by the oceans, decreasing seawater pH. We performed a mesocosm experiment in the Baltic Sea in order to investigate the consequences of increasing CO2 levels on pelagic carbon fluxes. A gradient of different CO2 scenarios, ranging

  1. Intertidal zones as carbon dioxide sources to coastal oceans

    Digital Repository Service at National Institute of Oceanography (India)

    DileepKumar, M.; George, M.D.; Rajagopal, M.D.

    To understand the factors controlling carbon dioxide (CO sub(2)) exchanges near land-sea boundary diurnal observations have been made twice on CO sub(2) in the air and water in a coastal region. The results suggest that CO sub(2) enrichment...

  2. Fingerprints of changes in the terrestrial carbon cycle in response to large reorganizations in ocean circulation

    Directory of Open Access Journals (Sweden)

    A. Bozbiyik

    2011-03-01

    Full Text Available CO2 and carbon cycle changes in the land, ocean and atmosphere are investigated using the comprehensive carbon cycle-climate model NCAR CSM1.4-carbon. Ensemble simulations are forced with freshwater perturbations applied at the North Atlantic and Southern Ocean deep water formation sites under pre-industrial climate conditions. As a result, the Atlantic Meridional Overturning Circulation reduces in each experiment to varying degrees. The physical climate fields show changes qualitatively in agreement with results documented in the literature, but there is a clear distinction between northern and southern perturbations. Changes in the physical variables, in turn, affect the land and ocean biogeochemical cycles and cause a reduction, or an increase, in the atmospheric CO2 concentration by up to 20 ppmv, depending on the location of the perturbation. In the case of a North Atlantic perturbation, the land biosphere reacts with a strong reduction in carbon stocks in some tropical locations and in high northern latitudes. In contrast, land carbon stocks tend to increase in response to a southern perturbation. The ocean is generally a sink of carbon although large reorganizations occur throughout various basins. The response of the land biosphere is strongest in the tropical regions due to a shift of the Intertropical Convergence Zone. The carbon fingerprints of this shift, either to the south or to the north depending on where the freshwater is applied, can be found most clearly in South America. For this reason, a compilation of various paleoclimate proxy records of Younger Dryas precipitation changes are compared with our model results. The proxy records, in general, show good agreement with the model's response to a North Atlantic freshwater perturbation.

  3. Climate change and ocean acidification impacts on lower trophic levels and the export of organic carbon to the deep ocean

    Directory of Open Access Journals (Sweden)

    A. Yool

    2013-09-01

    Full Text Available Most future projections forecast significant and ongoing climate change during the 21st century, but with the severity of impacts dependent on efforts to restrain or reorganise human activity to limit carbon dioxide (CO2 emissions. A major sink for atmospheric CO2, and a key source of biological resources, the World Ocean is widely anticipated to undergo profound physical and – via ocean acidification – chemical changes as direct and indirect results of these emissions. Given strong biophysical coupling, the marine biota is also expected to experience strong changes in response to this anthropogenic forcing. Here we examine the large-scale response of ocean biogeochemistry to climate and acidification impacts during the 21st century for Representative Concentration Pathways (RCPs 2.6 and 8.5 using an intermediate complexity global ecosystem model, MEDUSA-2.0. The primary impact of future change lies in stratification-led declines in the availability of key nutrients in surface waters, which in turn leads to a global decrease (1990s vs. 2090s in ocean productivity (−6.3%. This impact has knock-on consequences for the abundance of the low trophic level biogeochemical actors modelled by MEDUSA-2.0 (−5.8%, and these would be expected to similarly impact higher trophic level elements such as fisheries. Related impacts are found in the flux of organic material to seafloor communities (−40.7% at 1000 m, and in the volume of ocean suboxic zones (+12.5%. A sensitivity analysis removing an acidification feedback on calcification finds that change in this process significantly impacts benthic communities, suggesting that a~better understanding of the OA-sensitivity of calcifying organisms, and their role in ballasting sinking organic carbon, may significantly improve forecasting of these ecosystems. For all processes, there is geographical variability in change – for instance, productivity declines −21% in the Atlantic and increases +59% in

  4. Comparison of carbon uptake estimates from forest inventory and Eddy-Covariance for a montane rainforest in central Sulawesi

    Science.gov (United States)

    Heimsch, Florian; Kreilein, Heiner; Rauf, Abdul; Knohl, Alexander

    2016-04-01

    Rainforests in general and montane rainforests in particular have rarely been studied over longer time periods. We aim to provide baseline information of a montane tropical forest's carbon uptake over time in order to quantify possible losses through land-use change. Thus we conducted a re-inventory of 22 10-year old forest inventory plots, giving us a rare opportunity to quantify carbon uptake over such a long time period by traditional methods. We discuss shortfalls of such techniques and why our estimate of 1.5 Mg/ha/a should be considered as the lower boundary and not the mean carbon uptake per year. At the same location as the inventory, CO2 fluxes were measured with the Eddy-Covariance technique. Measurements were conducted at 48m height with an LI 7500 open-path infrared gas analyser. We will compare carbon uptake estimates from these measurements to those of the more conventional inventory method and discuss, which factors are probably responsible for differences.

  5. A probabilistic assessment of calcium carbonate export and dissolution in the modern ocean

    OpenAIRE

    Battaglia Gianna; Steinacher Marco; Joos Fortunat

    2016-01-01

    The marine cycle of calcium carbonate (CaCO3) is an important element of the carbon cycle and co-governs the distribution of carbon and alkalinity within the ocean. However, CaCO3 export fluxes and mechanisms governing CaCO3 dissolution are highly uncertain. We present an observationally constrained, probabilistic assessment of the global and regional CaCO3 budgets. Parameters governing pelagic CaCO3 export fluxes and dissolution rates are sampled using a Monte Carlo sche...

  6. Informing climate models with rapid chamber measurements of forest carbon uptake.

    Science.gov (United States)

    Metcalfe, Daniel B; Ricciuto, Daniel; Palmroth, Sari; Campbell, Catherine; Hurry, Vaughan; Mao, Jiafu; Keel, Sonja G; Linder, Sune; Shi, Xiaoying; Näsholm, Torgny; Ohlsson, Klas E A; Blackburn, M; Thornton, Peter E; Oren, Ram

    2017-05-01

    Models predicting ecosystem carbon dioxide (CO 2 ) exchange under future climate change rely on relatively few real-world tests of their assumptions and outputs. Here, we demonstrate a rapid and cost-effective method to estimate CO 2 exchange from intact vegetation patches under varying atmospheric CO 2 concentrations . We find that net ecosystem CO 2 uptake (NEE) in a boreal forest rose linearly by 4.7 ± 0.2% of the current ambient rate for every 10 ppm CO 2 increase, with no detectable influence of foliar biomass, season, or nitrogen (N) fertilization. The lack of any clear short-term NEE response to fertilization in such an N-limited system is inconsistent with the instantaneous downregulation of photosynthesis formalized in many global models. Incorporating an alternative mechanism with considerable empirical support - diversion of excess carbon to storage compounds - into an existing earth system model brings the model output into closer agreement with our field measurements. A global simulation incorporating this modified model reduces a long-standing mismatch between the modeled and observed seasonal amplitude of atmospheric CO 2 . Wider application of this chamber approach would provide critical data needed to further improve modeled projections of biosphere-atmosphere CO 2 exchange in a changing climate. © 2016 John Wiley & Sons Ltd.

  7. Detecting carbon uptake and cellular allocation by individual algae in multispecies assemblages: Tracking carbon into single algal cells

    Energy Technology Data Exchange (ETDEWEB)

    Murdock, Justin N. [USDA Agricultural Research Service, National Sedimentation Laboratory, Oxford Mississippi; Department of Biology, Tennessee Technological University, Cookeville Tennessee

    2015-11-03

    Algal species vary in carbon (C) need and uptake rates. Understanding differences in C uptake and cellular allocation among species from natural communities will bring new insight into many ecosystem process questions including how species changes will alter energy availability and C sequestration in aquatic ecosystems. A major limitation of current methods that measure algal C incorporation is the inability to separate the response of individual species from mixed-species assemblages. I used Fourier-transform infrared microspectroscopy to qualitatively measure inorganic 13C isotope incorporation into individual algal cells in single species, two species, and natural phytoplankton assemblages. Lateral shifts in spectral peaks from 13C treatments were observed in all species. Comparison of peaks associated with carbohydrates, proteins, and lipids allowed for the detection of which individuals took in C, and which macromolecules the C was used to make. For example, shifts in Spirogyra spectral peaks showed substantial C incorporation in carbohydrates. Further, shifts in peaks at 1160 cm-1, 1108 cm-1, 1080 cm-1, 1048 cm-1, and 1030 cm-1 suggested C was being allocated into cellulose. The natural phytoplankton assemblage demonstrated how C could be tracked into co-occurring species. A diatom had large shifts in protein and carbohydrate peaks, while a green alga and euglenoid had only a few shifts in protein related peaks. Fourier-transform infrared microspectroscopy is an established, label free method for measuring the chemical composition of algal cells. However, adding a label such as 13C isotope can greatly expand the technique's capabilities by qualitatively tracking C movement between inorganic and organic states within single cells.

  8. Global assessment of ocean carbon export by combining satellite observations and food-web models

    Science.gov (United States)

    Siegel, D. A.; Buesseler, K. O.; Doney, S. C.; Sailley, S. F.; Behrenfeld, M. J.; Boyd, P. W.

    2014-03-01

    The export of organic carbon from the surface ocean by sinking particles is an important, yet highly uncertain, component of the global carbon cycle. Here we introduce a mechanistic assessment of the global ocean carbon export using satellite observations, including determinations of net primary production and the slope of the particle size spectrum, to drive a food-web model that estimates the production of sinking zooplankton feces and algal aggregates comprising the sinking particle flux at the base of the euphotic zone. The synthesis of observations and models reveals fundamentally different and ecologically consistent regional-scale patterns in export and export efficiency not found in previous global carbon export assessments. The model reproduces regional-scale particle export field observations and predicts a climatological mean global carbon export from the euphotic zone of 6 Pg C yr-1. Global export estimates show small variation (typically model parameter values. The model is also robust to the choices of the satellite data products used and enables interannual changes to be quantified. The present synthesis of observations and models provides a path for quantifying the ocean's biological pump.

  9. Efficiency and effects of carbon sequestration through ocean fertilization: results from a model study

    Energy Technology Data Exchange (ETDEWEB)

    Anand Gnanadesikan; Jorge L. Sarmiento; Richard D. Slater [NOAA/Geophysical Fluid Dynamics Laboratory, Princeton, NJ (United States)

    2003-07-01

    Simulations of ocean fertilization, which is patchy in space and time, were carried out using a simple model of nutrient cycling embedded in an ocean general circulation model which is integrated for 100 years. The fraction of the transient pulse of carbon produced by fertilization that comes out of the atmosphere is highly variable (ranging from 2%-44%). This fraction depends on the details of the long-term fate of the nutrients added as part of the fertilization, making verification of carbon sequestration extremely difficult. Additionally, in cases where fertilization removes nutrients from the surface layer, the result is to cause a decrease in production at subsequent times. These effects need to be taken into account when the impacts of fertilization on atmospheric carbon dioxide are evaluated. 10 refs., 1 fig., 1 tab.

  10. Climate change increases riverine carbon outgassing, while export to the ocean remains uncertain

    Science.gov (United States)

    Langerwisch, F.; Walz, A.; Rammig, A.; Tietjen, B.; Thonicke, K.; Cramer, W.

    2016-07-01

    Any regular interaction of land and river during flooding affects carbon pools within the terrestrial system, riverine carbon and carbon exported from the system. In the Amazon basin carbon fluxes are considerably influenced by annual flooding, during which terrigenous organic material is imported to the river. The Amazon basin therefore represents an excellent example of a tightly coupled terrestrial-riverine system. The processes of generation, conversion and transport of organic carbon in such a coupled terrigenous-riverine system strongly interact and are climate-sensitive, yet their functioning is rarely considered in Earth system models and their response to climate change is still largely unknown. To quantify regional and global carbon budgets and climate change effects on carbon pools and carbon fluxes, it is important to account for the coupling between the land, the river, the ocean and the atmosphere. We developed the RIVerine Carbon Model (RivCM), which is directly coupled to the well-established dynamic vegetation and hydrology model LPJmL, in order to account for this large-scale coupling. We evaluate RivCM with observational data and show that some of the values are reproduced quite well by the model, while we see large deviations for other variables. This is mainly caused by some simplifications we assumed. Our evaluation shows that it is possible to reproduce large-scale carbon transport across a river system but that this involves large uncertainties. Acknowledging these uncertainties, we estimate the potential changes in riverine carbon by applying RivCM for climate forcing from five climate models and three CO2 emission scenarios (Special Report on Emissions Scenarios, SRES). We find that climate change causes a doubling of riverine organic carbon in the southern and western basin while reducing it by 20 % in the eastern and northern parts. In contrast, the amount of riverine inorganic carbon shows a 2- to 3-fold increase in the entire basin

  11. Contrasting effects of temperature and winter mixing on the seasonal and inter-annual variability of the carbonate system in the Northeast Atlantic Ocean

    Directory of Open Access Journals (Sweden)

    C. Dumousseaud

    2010-05-01

    Full Text Available Future climate change as a result of increasing atmospheric CO2 concentrations is expected to strongly affect the oceans, with shallower winter mixing and consequent reduction in primary production and oceanic carbon drawdown in low and mid-latitudinal oceanic regions. Here we test this hypothesis by examining the effects of cold and warm winters on the carbonate system in the surface waters of the Northeast Atlantic Ocean for the period between 2005 and 2007. Monthly observations were made between the English Channel and the Bay of Biscay using a ship of opportunity program. During the colder winter of 2005/2006, the maximum depth of the mixed layer reached up to 650 m in the Bay of Biscay, whilst during the warmer (by 2.6 ± 0.5 °C winter of 2006/2007 the mixed layer depth reached only 300 m. The inter-annual differences in late winter concentrations of nitrate (2.8 ± 1.1 μmol l−1 and dissolved inorganic carbon (22 ± 6 μmol kg−1, with higher concentrations at the end of the colder winter (2005/2006, led to differences in the dissolved oxygen anomaly and the chlorophyll α-fluorescence data for the subsequent growing season. In contrast to model predictions, the calculated air-sea CO2 fluxes (ranging from +3.7 to −4.8 mmol m−2 d−1 showed an increased oceanic CO2 uptake in the Bay of Biscay following the warmer winter of 2006/2007 associated with wind speed and sea surface temperature differences.

  12. Repeated Storage of Respired Carbon in the Equatorial Pacific Ocean Over the Last Three Glacial Cycles

    Science.gov (United States)

    Jacobel, A. W.; McManus, J. F.; Anderson, R. F.; Winckler, G.

    2017-12-01

    As the largest reservoir of carbon actively exchanging with the atmosphere on glacial-interglacial timescales, the deep ocean has been implicated as the likely location of carbon dioxide sequestration during Pleistocene glaciations. Despite strong theoretical underpinnings for this expectation, it has been challenging to identify unequivocal evidence for respired carbon storage in the paleoceanographic record. Data on the rate of ocean ventilation derived from paired planktonic-benthic foraminifera radiocarbon ages conflict across the equatorial Pacific, and different proxy reconstructions contradict one another about the depth and origin of the watermass containing the respired carbon. Because any change in the storage of respiratory carbon must be accompanied by corresponding changes in dissolved oxygen concentrations, proxy data reflecting bottom water oxygenation are of value in addressing these apparent inconsistencies. We present new records of the redox sensitive metal uranium from the central equatorial Pacific to qualitatively identify intervals associated with respiratory carbon storage over the past 350 kyr. Our data reveal periods of deep ocean authigenic uranium deposition in association with each of the last three glacial maxima. Equatorial Pacific export productivity data show intervals with abundant authigenic uranium are not associated with local productivity increases, indicating episodic precipitation of authigenic uranium does not directly reflect increases in situ microbial respiration, but rather occurs in response to basin-wide decreases in deep water oxygen concentrations. We combine our new data with previously published results to propose a picture of glacial carbon storage and equatorial Pacific watermass structure that is internally consistent. We conclude that respired carbon storage in the Pacific was a persistent feature of Pleistocene glaciations.

  13. Carbon and nitrogen fluxes in the North Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Naqvi, S.W.A.; Naik, H.; DeSouza, W.; Narvekar, P.V.; Paropkari, A.L.; Bange, H.W.

    , the reverse is probably true for the burial. Notwithstanding these uncertainties, it seems reasonable to conclude that the POC delivery by rivers substantially exceeds sedimentary organic carbon burial in the NEIO. In spite of the higher sedimentation... in the NEIO has been reported to range from 0.3 to 2.5 (average 1.4) Tg N yr -1 (Schäfer et al., 1993). This is slightly higher than the DIN delivery by rivers. Rate of N 2 -fixation in the NEIO has not been measured so far. However, it is probably much...

  14. Bioinformatic analysis of the distribution of inorganic carbon transporters and prospective targets for bioengineering to increase Ci uptake by cyanobacteria.

    Science.gov (United States)

    Gaudana, Sandeep B; Zarzycki, Jan; Moparthi, Vamsi K; Kerfeld, Cheryl A

    2015-10-01

    Cyanobacteria have evolved a carbon-concentrating mechanism (CCM) which has enabled them to inhabit diverse environments encompassing a range of inorganic carbon (Ci: [Formula: see text] and CO2) concentrations. Several uptake systems facilitate inorganic carbon accumulation in the cell, which can in turn be fixed by ribulose 1,5-bisphosphate carboxylase/oxygenase. Here we survey the distribution of genes encoding known Ci uptake systems in cyanobacterial genomes and, using a pfam- and gene context-based approach, identify in the marine (alpha) cyanobacteria a heretofore unrecognized number of putative counterparts to the well-known Ci transporters of beta cyanobacteria. In addition, our analysis shows that there is a huge repertoire of transport systems in cyanobacteria of unknown function, many with homology to characterized Ci transporters. These can be viewed as prospective targets for conversion into ancillary Ci transporters through bioengineering. Increasing intracellular Ci concentration coupled with efforts to increase carbon fixation will be beneficial for the downstream conversion of fixed carbon into value-added products including biofuels. In addition to CCM transporter homologs, we also survey the occurrence of rhodopsin homologs in cyanobacteria, including bacteriorhodopsin, a class of retinal-binding, light-activated proton pumps. Because they are light driven and because of the apparent ease of altering their ion selectivity, we use this as an example of re-purposing an endogenous transporter for the augmentation of Ci uptake by cyanobacteria and potentially chloroplasts.

  15. Uptake and cytotoxic effects of multi-walled carbon nanotubes in human bronchial epithelial cells

    International Nuclear Information System (INIS)

    Hirano, Seishiro; Fujitani, Yuji; Furuyama, Akiko; Kanno, Sanae

    2010-01-01

    Carbon nanotubes (CNT) are cytotoxic to several cell types. However, the mechanism of CNT toxicity has not been fully studied, and dosimetric analyses of CNT in the cell culture system are lacking. Here, we describe a novel, high throughput method to measure cellular uptake of CNT using turbimetry. BEAS-2B, a human bronchial epithelial cell line, was used to investigate cellular uptake, cytotoxicity, and inflammatory effects of multi-walled CNT (MWCNT). The cytotoxicity of MWCNT was higher than that of crocidolite asbestos in BEAS-2B cells. The IC 50 of MWCNT was 12 μg/ml, whereas that of asbestos (crocidolite) was 678 μg/ml. Over the course of 5 to 8 h, BEAS-2B cells took up 17-18% of the MWCNT when they were added to the culture medium at a concentration of 10 μg/ml. BEAS-2B cells were exposed to 2, 5, or 10 μg/ml of MWCNT, and total RNA was extracted for cytokine cDNA primer array assays. The culture supernatant was collected for cytokine antibody array assays. Cytokines IL-6 and IL-8 increased in a dose dependent manner at both the mRNA and protein levels. Migration inhibitory factor (MIF) also increased in the culture supernatant in response to MWCNT. A phosphokinase array study using lysates from BEAS-2B cells exposed to MWCNT indicated that phosphorylation of p38, ERK1, and HSP27 increased significantly in response to MWCNT. Results from a reporter gene assays using the NF-κB or AP-1 promoter linked to the luciferase gene in transiently transfected CHO-KI cells revealed that NF-κB was activated following MWCNT exposure, while AP-1 was not changed. Collectively, MWCNT activated NF-κB, enhanced phosphorylation of MAP kinase pathway components, and increased production of proinflammatory cytokines in human bronchial epithelial cells.

  16. Evaluating Southern Ocean Carbon Eddy-Pump From Biogeochemical-Argo Floats

    Science.gov (United States)

    Llort, Joan; Langlais, C.; Matear, R.; Moreau, S.; Lenton, A.; Strutton, Peter G.

    2018-02-01

    The vertical transport of surface water and carbon into ocean's interior, known as subduction, is one of the main mechanisms through which the ocean influences Earth's climate. New instrumental approaches have shown the occurrence of localized and intermittent subduction episodes associated with small-scale ocean circulation features. These studies also revealed the importance of such events for the export of organic matter, the so-called eddy-pump. However, the transient and localized nature of episodic subduction hindered its large-scale evaluation to date. In this work, we present an approach to detect subduction events at the scale of the Southern Ocean using measurements collected by biogeochemical autonomous floats (BGCArgo). We show how subduction events can be automatically identified as anomalies of spiciness and Apparent Oxygen Utilization (AOU) below the mixed layer. Using this methodology over more than 4,000 profiles, we detected 40 subduction events unevenly distributed across the Sothern Ocean. Events were more likely found in hot spots of eddy kinetic energy (EKE), downstream major bathymetric features. Moreover, the bio-optical measurements provided by BGCArgo allowed measuring the amount of Particulate Organic Carbon (POC) being subducted and assessing the contribution of these events to the total downward carbon flux at 100 m (EP100). We estimated that the eddy-pump represents less than 19% to the EP100 in the Southern Ocean, although we observed particularly strong events able to locally duplicate the EP100. This approach provides a novel perspective on where episodic subduction occurs that will be naturally improved as BGCArgo observations continue to increase.

  17. Assessing global carbon burial during Oceanic Anoxic Event 2, Cenomanian-Turonian boundary event

    Science.gov (United States)

    Owens, J. D.; Lyons, T. W.; Lowery, C. M.

    2017-12-01

    Reconstructing the areal extent and total amount of organic carbon burial during ancient events remains elusive even for the best documented oceanic anoxic event (OAE) in Earth history, the Cenomanian-Turonian boundary event ( 93.9 Ma), or OAE 2. Reports from 150 OAE 2 localities provide a wide global distribution. However, despite the large number of sections, the majority are found within the proto-Atlantic and Tethyan oceans and interior seaways. Considering these gaps in spatial coverage, the pervasive increase in organic carbon (OC) burial during OAE2 that drove carbon isotope values more positive (average of 4‰) can provide additional insight. These isotope data allow us to estimate the total global burial of OC, even for unstudied portions of the global ocean. Thus, we can solve for any `missing' OC sinks by comparing our estimates from a forward carbon-isotope box model with the known, mapped distribution of OC for OAE 2 sediments. Using the known OC distribution and reasonably extrapolating to the surrounding regions of analogous depositional conditions accounts for only 13% of the total seafloor, mostly in marginal marine settings. This small geographic area accounts for more OC burial than the entire modern ocean, but significantly less than the amount necessary to produce the observed isotope record. Using modern and OAE 2 average OC rates we extrapolate further to appropriate depositional settings in the unknown portions of seafloor, mostly deep abyssal plains. This addition significantly increases the predicted amount buried but still does not account for total burial. Additional sources, including hydrocarbon migration, lacustrine, and coal also cannot account for the missing OC. This difference points to unknown portions of the open ocean with high TOC contents or exceptionally high TOC in productive marginal marine regions, which are underestimated in our extrapolations. This difference might be explained by highly productive margins within the

  18. Nitrogen and phosphorous limitation reduces the effects of land use change on land carbon uptake or emission

    International Nuclear Information System (INIS)

    Wang, Ying-Ping; Zhang, Qian; Dai, Yongjiu; Pitman, Andrew J

    2015-01-01

    We used an Earth System Model that includes both nitrogen (N) and phosphorus (P) cycling to simulate the impacts of land-use and land-cover change (LULCC) for two representative concentration pathways (RCPs): a reforestation scenario (RCP4.5) and a deforestation scenario (RCP8.5). For each RCP, we performed simulations with and without LULCC using the carbon (C only) mode or including the full C, N and P cycles (CNP). We show, for the first time, that inclusion of N and P cycling reduces both the carbon uptake from reforestation in RCP4.5 and the carbon emission from deforestation in RCP8.5. Specifically, carbon-nutrient interaction reduces carbon uptake in RCP4.5 from 55 Pg C (C only) to 21 Pg C (CNP), or the emissions in RCP8.5 from 72 Pg C (C only) to 56 Pg C (CNP). Most of those reductions result from much weaker responses of net primary production to CO 2 fertilization and climate change when carbon-nutrient interaction is taken into account, as compared to C only simulations. Our results highlight the importance of including nutrient-carbon interaction in estimating the carbon benefit from reforestation and carbon loss from deforestation in a future world with higher CO 2 and a warmer climate. Because of the stronger nutrient limitation, carbon gain from reforestation in the temperate and boreal regions is much less than the carbon loss from deforestation in the subtropical and tropical regions from 2006 to 2100 for the two RCPs. Therefore protecting the existing subtropical and tropical forests is about twice as effective as planting new forests in the temperate and boreal regions for climate mitigation. (letter)

  19. An Ocean Sediment Core-Top Calibration of Foraminiferal (Cibicides) Stable Carbon Isotope Ratios

    Science.gov (United States)

    Schmittner, A.; Mix, A. C.; Lisiecki, L. E.; Peterson, C.; Mackensen, A.; Cartapanis, O. A.

    2015-12-01

    Stable carbon isotope ratios (δ13C) measured on calcium carbonate shells of benthic foraminifera (cibicides) from late Holocene sediments (δ13CCib) are compiled and compared with newly updated datasets of contemporary water-column δ13C observations of dissolved inorganic carbon (δ13CDIC) as the initial core-top calibration of the international Ocean Circulation and CarbonCycling (OC3) project. Using selection criteria based on the spatial distance between samples we find high correlation between δ13CCib and natural (pre-industrial) δ13CDIC, confirming earlier work. However, our analysis reveals systematic differences such as higher (lower) δ13CCib values in the Atlantic (Indian and Pacific) oceans. Regression analyses are impacted by anthropogenic carbon and suggest significant carbonate ion, temperature, and pressure effects, consistent with lab experiments with planktonic foraminifera and theory. The estimated standard error of core-top sediment data is generally σ ~= 0.25 ‰, whereas modern foram data from the South Atlantic indicate larger errors (σ ~= 0.4 ‰).

  20. Biological production in the Indian Ocean upwelling zones - Part 1: refined estimation via the use of a variable compensation depth in ocean carbon models

    Science.gov (United States)

    Geethalekshmi Sreeush, Mohanan; Valsala, Vinu; Pentakota, Sreenivas; Venkata Siva Rama Prasad, Koneru; Murtugudde, Raghu

    2018-04-01

    Biological modelling approach adopted by the Ocean Carbon-Cycle Model Intercomparison Project (OCMIP-II) provided amazingly simple but surprisingly accurate rendition of the annual mean carbon cycle for the global ocean. Nonetheless, OCMIP models are known to have seasonal biases which are typically attributed to their bulk parameterisation of compensation depth. Utilising the criteria of surface Chl a-based attenuation of solar radiation and the minimum solar radiation required for production, we have proposed a new parameterisation for a spatially and temporally varying compensation depth which captures the seasonality in the production zone reasonably well. This new parameterisation is shown to improve the seasonality of CO2 fluxes, surface ocean pCO2, biological export and new production in the major upwelling zones of the Indian Ocean. The seasonally varying compensation depth enriches the nutrient concentration in the upper ocean yielding more faithful biological exports which in turn leads to accurate seasonality in the carbon cycle. The export production strengthens by ˜ 70 % over the western Arabian Sea during the monsoon period and achieves a good balance between export and new production in the model. This underscores the importance of having a seasonal balance in the model export and new productions for a better representation of the seasonality of the carbon cycle over upwelling regions. The study also implies that both the biological and solubility pumps play an important role in the Indian Ocean upwelling zones.

  1. Correlation Lengths for Estimating the Large-Scale Carbon and Heat Content of the Southern Ocean

    Science.gov (United States)

    Mazloff, M. R.; Cornuelle, B. D.; Gille, S. T.; Verdy, A.

    2018-02-01

    The spatial correlation scales of oceanic dissolved inorganic carbon, heat content, and carbon and heat exchanges with the atmosphere are estimated from a realistic numerical simulation of the Southern Ocean. Biases in the model are assessed by comparing the simulated sea surface height and temperature scales to those derived from optimally interpolated satellite measurements. While these products do not resolve all ocean scales, they are representative of the climate scale variability we aim to estimate. Results show that constraining the carbon and heat inventory between 35°S and 70°S on time-scales longer than 90 days requires approximately 100 optimally spaced measurement platforms: approximately one platform every 20° longitude by 6° latitude. Carbon flux has slightly longer zonal scales, and requires a coverage of approximately 30° by 6°. Heat flux has much longer scales, and thus a platform distribution of approximately 90° by 10° would be sufficient. Fluxes, however, have significant subseasonal variability. For all fields, and especially fluxes, sustained measurements in time are required to prevent aliasing of the eddy signals into the longer climate scale signals. Our results imply a minimum of 100 biogeochemical-Argo floats are required to monitor the Southern Ocean carbon and heat content and air-sea exchanges on time-scales longer than 90 days. However, an estimate of formal mapping error using the current Argo array implies that in practice even an array of 600 floats (a nominal float density of about 1 every 7° longitude by 3° latitude) will result in nonnegligible uncertainty in estimating climate signals.

  2. Positron emission tomography shows high specific uptake of racemic carbon-11 labelled norepinephrine in the primate heart

    International Nuclear Information System (INIS)

    Farde, L.; Halldin, C.; Naagren, K.; Suhara, Tetsuya; Karlsson, P.; Schoeps, K.O.; Swahn, C.G.; Bone, D.

    1994-01-01

    (-)-Norepinephrine is the predominant neurotransmitter of the sympathetic innervation of the heart. Racemic norepinephrine was labelled with carbon-11 and injected i.v. into Cynomolgus monkeys. Five minutes after injection there was a more than tenfold higher radioactivity in the heart than in adjacent tissue. Pretreatment with the norepinephrine reuptake inhibitor desipramine reduced the uptake by more than 80%. The high specific uptake of racemic [ 11 C]norepinephrine indicates that enatiomerically pure(-)-[ 11 C]norepinephrine has promising potential for detailed mapping of the sympathetic innervation of the human myocardium. (orig.)

  3. Positron emission tomography shows high specific uptake of racemic carbon-11 labelled norepinephrine in the primate heart

    Energy Technology Data Exchange (ETDEWEB)

    Farde, L [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden); Halldin, C [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden); Naagren, K [Turku Univ., Cyclotron/PET Center (Finland); Suhara, Tetsuya [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden); Karlsson, P [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden); Schoeps, K O [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden); Swahn, C G [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden); Bone, D [Dept. of Clinical Neuroscience, Karolinska Inst., Stockholm (Sweden)

    1994-04-01

    (-)-Norepinephrine is the predominant neurotransmitter of the sympathetic innervation of the heart. Racemic norepinephrine was labelled with carbon-11 and injected i.v. into Cynomolgus monkeys. Five minutes after injection there was a more than tenfold higher radioactivity in the heart than in adjacent tissue. Pretreatment with the norepinephrine reuptake inhibitor desipramine reduced the uptake by more than 80%. The high specific uptake of racemic [[sup 11]C]norepinephrine indicates that enatiomerically pure(-)-[[sup 11]C]norepinephrine has promising potential for detailed mapping of the sympathetic innervation of the human myocardium. (orig.)

  4. Global patterns of organic carbon export and sequestration in the ocean (Arne Richter Award for Outstanding Young Scientists)

    Science.gov (United States)

    Henson, S.; Sanders, R.; Madsen, E.; Le Moigne, F.; Quartly, G.

    2012-04-01

    A major term in the global carbon cycle is the ocean's biological carbon pump which is dominated by sinking of small organic particles from the surface ocean to its interior. Here we examine global patterns in particle export efficiency (PEeff), the proportion of primary production that is exported from the surface ocean, and transfer efficiency (Teff), the fraction of exported organic matter that reaches the deep ocean. This is achieved through extrapolating from in situ estimates of particulate organic carbon export to the global scale using satellite-derived data. Global scale estimates derived from satellite data show, in keeping with earlier studies, that PEeff is high at high latitudes and low at low latitudes, but that Teff is low at high latitudes and high at low latitudes. However, in contrast to the relationship observed for deep biomineral fluxes in previous studies, we find that Teff is strongly negatively correlated with opal export flux from the upper ocean, but uncorrelated with calcium carbonate export flux. We hypothesise that the underlying factor governing the spatial patterns observed in Teff is ecosystem function, specifically the degree of recycling occurring in the upper ocean, rather than the availability of calcium carbonate for ballasting. Finally, our estimate of global integrated carbon export is only 50% of previous estimates. The lack of consensus amongst different methodologies on the strength of the biological carbon pump emphasises that our knowledge of a major planetary carbon flux remains incomplete.

  5. The role of destabilization of palladium hydride in the hydrogen uptake of Pd-containing activated carbons

    International Nuclear Information System (INIS)

    Bhat, V V; Contescu, C I; Gallego, N C

    2009-01-01

    This paper reports on differences in stability of Pd hydride phases in palladium particles with various degrees of contact with microporous carbon supports. A sample containing Pd embedded in activated carbon fibre (2 wt% Pd) was compared with commercial Pd nanoparticles deposited on microporous activated carbon (3 wt% Pd) and with support-free nanocrystalline palladium. The morphology of the materials was characterized by electron microscopy, and the phase transformations were analysed over a large range of hydrogen partial pressures (0.003-10 bar) and at several temperatures using in situ x-ray diffraction. The results were verified with volumetric hydrogen uptake measurements. Results indicate that higher degrees of Pd-carbon contacts for Pd particles embedded in a microporous carbon matrix induce efficient 'pumping' of hydrogen out of β- PdH x . It was also found that thermal cleaning of carbon surface groups prior to exposure to hydrogen further enhances the hydrogen pumping power of the microporous carbon support. In brief, this study highlights that the stability of β- PdH x phase supported on carbon depends on the degree of contact between Pd and carbon and on the nature of the carbon surface.

  6. Valuing multiple eelgrass ecosystem services in Sweden: fish production and uptake of carbon and nitrogen

    Directory of Open Access Journals (Sweden)

    Scott Glenn Cole

    2016-01-01

    Full Text Available Valuing nature’s benefits in monetary terms is necessary for policy-makers facing trade-offs in how to spend limited financial resources on environmental protection. We provide information to assess trade-offs associated with the management of seagrass beds, which provide a number of ecosystem services, but are presently impacted by many stressors. We develop an interdisciplinary framework for valuing multiple ecosystem services and apply it to the case of eelgrass (Zostera marina, a dominant seagrass species in the northern hemisphere. We identify and quantify links between three eelgrass functions (habitat for fish, carbon and nitrogen uptake and economic goods in Sweden, quantify these using ecological endpoints, estimate the marginal average value of the impact of losing one hectare of eelgrass along the Swedish northwest coast on welfare in monetary terms, and aggregate these values while considering double-counting. Over a 20 to 50 year period we find that compared to unvegetated habitats, a hectare of eelgrass, including the organic material accumulated in the sediment, produces an additional 626 kg cod fishes and 7,535 wrasse individuals and sequesters 98.6 ton carbon and 466 kg nitrogen. We value the flow of future benefits associated with commercial fishing, avoided climate change damages, and reduced eutrophication at 170,000 SEK in 2014 (20,700 US$ or 11,000 SEK (1,300 US$ annualized at 4%. Fish production, which is the most commonly valued ecosystem service in the seagrass literature, only represented 25% of the total value whereas a conservative estimate of nitrogen regulation constituted 46%, suggesting that most seagrass beds are undervalued. Comparing these values with historic losses of eelgrass we show that the Swedish northwest coast has suffered a substantial reduction in fish production and mineral regulation. Future work should improve the understanding of the geographic scale of eelgrass functions, how local variables

  7. Quantitative evaluation of multi-walled carbon nanotube uptake in wheat and rapeseed

    Energy Technology Data Exchange (ETDEWEB)

    Larue, Camille, E-mail: Camille.larue@cea.fr [UMR3299 CEA-CNRS, Service Interdisciplinaire des Systemes Moleculaires et Materiaux, Laboratoire Structure et Dynamique par Resonance Magnetique (LSDRM), CEA Saclay, 91191 Gif sur Yvette (France); Pinault, Mathieu, E-mail: Mathieu.pinault@cea.fr [CEA, IRAMIS, SPAM, Laboratoire Francis Perrin (CNRS URA 2453), 91191 Gif sur Yvette (France); Czarny, Bertrand, E-mail: Bertrand.czarny@cea.fr [CEA, iBiTecS SIMOPRO, CEA Saclay, 91191 Gif sur Yvette (France); Georgin, Dominique, E-mail: Dominique.georgin@cea.fr [CEA, IBiTecS, SCBM, CEA Saclay, 91191 Gif sur Yvette (France); Jaillard, Danielle, E-mail: danielle.jaillard@u-psud.fr [UMR8195 CNRS-Universite Paris-Sud, Centre Commun de Microscopie Electronique, F-91405 Orsay (France); Bendiab, Nedjma, E-mail: Nedjma.bendiab@grenoble.cnrs.fr [Institut Neel, CNRS-Universite Joseph Fourier, 25 rue des Martyrs, 38049 Grenoble Cedex 9 (France); Mayne-L' Hermite, Martine, E-mail: martine.mayne@cea.fr [CEA, IRAMIS, SPAM, Laboratoire Francis Perrin (CNRS URA 2453), 91191 Gif sur Yvette (France); Taran, Frederic, E-mail: frederic.taran@cea.fr [CEA, IBiTecS, SCBM, CEA Saclay, 91191 Gif sur Yvette (France); Dive, Vincent, E-mail: vincent.dive@cea.fr [CEA, iBiTecS SIMOPRO, CEA Saclay, 91191 Gif sur Yvette (France); and others

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer Wheat and rapeseed accumulate MWCNT through root exposure, and translocate them to their leaves. Black-Right-Pointing-Pointer Transfer factor of MWCNT from hydroponic solution to leaves never exceeds 0.005 Per-Mille-Sign . Black-Right-Pointing-Pointer MWCNT majorly accumulate in the most peripheral areas and in newly developed leaves. Black-Right-Pointing-Pointer Accumulation of less than 200 ng MWCNT per g of leaf does not impact plant development and physiology. - Abstract: Environmental contamination with carbon nanotubes would lead to plant exposure and particularly exposure of agricultural crops. The only quantitative exposure data available to date which can be used for risk assessment comes from computer modeling. The aim of this study was to provide quantitative data relative to multi-walled carbon nanotube (MWCNT) uptake and distribution in agricultural crops, and to correlate accumulation data with impact on plant development and physiology. Roots of wheat and rapeseed were exposed in hydroponics to uniformly {sup 14}C-radiolabeled MWCNTs. Radioimaging, transmission electron microscopy and raman spectroscopy were used to identify CNT distribution. Radioactivity counting made it possible absolute quantification of CNT accumulation in plant leaves. Impact of CNTs on seed germination, root elongation, plant biomass, evapotranspiration, chlorophyll, thiobarbituric acid reactive species and H{sub 2}O{sub 2} contents was evaluated. We demonstrate that less than 0.005 Per-Mille-Sign of the applied MWCNT dose is taken up by plant roots and translocated to the leaves. This accumulation does not impact plant development and physiology. In addition, it does not induce any modifications in photosynthetic activity nor cause oxidative stress in plant leaves. Our results suggest that if environmental contamination occurs and MWCNTs are in the same physico-chemical state than the ones used in the present article, MWCNT transfer to

  8. Quantitative evaluation of multi-walled carbon nanotube uptake in wheat and rapeseed

    International Nuclear Information System (INIS)

    Larue, Camille; Pinault, Mathieu; Czarny, Bertrand; Georgin, Dominique; Jaillard, Danielle; Bendiab, Nedjma; Mayne-L’Hermite, Martine; Taran, Frédéric; Dive, Vincent

    2012-01-01

    Highlights: ► Wheat and rapeseed accumulate MWCNT through root exposure, and translocate them to their leaves. ► Transfer factor of MWCNT from hydroponic solution to leaves never exceeds 0.005‰. ► MWCNT majorly accumulate in the most peripheral areas and in newly developed leaves. ► Accumulation of less than 200 ng MWCNT per g of leaf does not impact plant development and physiology. - Abstract: Environmental contamination with carbon nanotubes would lead to plant exposure and particularly exposure of agricultural crops. The only quantitative exposure data available to date which can be used for risk assessment comes from computer modeling. The aim of this study was to provide quantitative data relative to multi-walled carbon nanotube (MWCNT) uptake and distribution in agricultural crops, and to correlate accumulation data with impact on plant development and physiology. Roots of wheat and rapeseed were exposed in hydroponics to uniformly 14 C-radiolabeled MWCNTs. Radioimaging, transmission electron microscopy and raman spectroscopy were used to identify CNT distribution. Radioactivity counting made it possible absolute quantification of CNT accumulation in plant leaves. Impact of CNTs on seed germination, root elongation, plant biomass, evapotranspiration, chlorophyll, thiobarbituric acid reactive species and H 2 O 2 contents was evaluated. We demonstrate that less than 0.005‰ of the applied MWCNT dose is taken up by plant roots and translocated to the leaves. This accumulation does not impact plant development and physiology. In addition, it does not induce any modifications in photosynthetic activity nor cause oxidative stress in plant leaves. Our results suggest that if environmental contamination occurs and MWCNTs are in the same physico-chemical state than the ones used in the present article, MWCNT transfer to the food chain via food crops would be very low.

  9. Predicting Phenologic Response to Water Stress and Implications for Carbon Uptake across the Southeast U.S.

    Science.gov (United States)

    Lowman, L.; Barros, A. P.

    2016-12-01

    Representation of plant photosynthesis in modeling studies requires phenologic indicators to scale carbon assimilation by plants. These indicators are typically the fraction of photosynthetically active radiation (FPAR) and leaf area index (LAI) which represent plant responses to light and water availability, as well as temperature constraints. In this study, a prognostic phenology model based on the growing season index is adapted to determine the phenologic indicators of LAI and FPAR at the sub-daily scale based on meteorological and soil conditions. Specifically, we directly model vegetation green-up and die-off responses to temperature, vapor pressure deficit, soil water potential, and incoming solar radiation. The indices are based on the properties of individual plant functional types, driven by observational data and prior modeling applications. First, we describe and test the sensitivity of the carbon uptake response to predicted phenology for different vegetation types. Second, the prognostic phenology model is incorporated into a land-surface hydrology model, the Duke Coupled Hydrology Model with Prognostic Vegetation (DCHM-PV), to demonstrate the impact of dynamic phenology on modeled carbon assimilation rates and hydrologic feedbacks. Preliminary results show reduced carbon uptake rates when incorporating a prognostic phenology model that match well against the eddy-covariance flux tower observations. Additionally, grassland vegetation shows the most variability in LAI and FPAR tied to meteorological and soil conditions. These results highlight the need to incorporate vegetation-specific responses to water limitation in order to accurately estimate the terrestrial carbon storage component of the global carbon budget.

  10. The seasonal sea-ice zone in the glacial Southern Ocean as a carbon sink.

    Science.gov (United States)

    Abelmann, Andrea; Gersonde, Rainer; Knorr, Gregor; Zhang, Xu; Chapligin, Bernhard; Maier, Edith; Esper, Oliver; Friedrichsen, Hans; Lohmann, Gerrit; Meyer, Hanno; Tiedemann, Ralf

    2015-09-18

    Reduced surface-deep ocean exchange and enhanced nutrient consumption by phytoplankton in the Southern Ocean have been linked to lower glacial atmospheric CO2. However, identification of the biological and physical conditions involved and the related processes remains incomplete. Here we specify Southern Ocean surface-subsurface contrasts using a new tool, the combined oxygen and silicon isotope measurement of diatom and radiolarian opal, in combination with numerical simulations. Our data do not indicate a permanent glacial halocline related to melt water from icebergs. Corroborated by numerical simulations, we find that glacial surface stratification was variable and linked to seasonal sea-ice changes. During glacial spring-summer, the mixed layer was relatively shallow, while deeper mixing occurred during fall-winter, allowing for surface-ocean refueling with nutrients from the deep reservoir, which was potentially richer in nutrients than today. This generated specific carbon and opal export regimes turning the glacial seasonal sea-ice zone into a carbon sink.

  11. Independence of nutrient limitation and carbon dioxide impacts on the Southern Ocean coccolithophore Emiliania huxleyi.

    Science.gov (United States)

    Müller, Marius N; Trull, Thomas W; Hallegraeff, Gustaaf M

    2017-08-01

    Future oceanic conditions induced by anthropogenic greenhouse gas emissions include warming, acidification and reduced nutrient supply due to increased stratification. Some parts of the Southern Ocean are expected to show rapid changes, especially for carbonate mineral saturation. Here we compare the physiological response of the model coccolithophore Emiliania huxleyi (strain EHSO 5.14, originating from 50 o S, 149 o E) with pH/CO 2 gradients (mimicking ocean acidification ranging from 1 to 4 × current pCO 2 levels) under nutrient-limited (nitrogen and phosphorus) and -replete conditions. Both nutrient limitations decreased per cell photosynthesis (particulate organic carbon (POC) production) and calcification (particulate inorganic carbon (PIC) production) rates for all pCO 2 levels, with more than 50% reductions under nitrogen limitation. These impacts, however, became indistinguishable from nutrient-replete conditions when normalized to cell volume. Calcification decreased three-fold and linearly with increasing pCO 2 under all nutrient conditions, and was accompanied by a smaller ~30% nonlinear reduction in POC production, manifested mainly above 3 × current pCO 2 . Our results suggest that normalization to cell volume allows the major impacts of nutrient limitation (changed cell sizes and reduced PIC and POC production rates) to be treated independently of the major impacts of increasing pCO 2 and, additionally, stresses the importance of including cell volume measurements to the toolbox of standard physiological analysis of coccolithophores in field and laboratory studies.

  12. An Innovative Concept for Spacebased Lidar Measurement of Ocean Carbon Biomass

    Science.gov (United States)

    Hu, Yongxiang; Behrenfeld, Michael; Hostetler, Chris; Pelon, Jacques; Trepte, Charles; Hair, John; Slade, Wayne; Cetinic, Ivona; Vaughan, Mark; Lu, Xiaomei; hide

    2015-01-01

    Beam attenuation coefficient, c, provides an important optical index of plankton standing stocks, such as phytoplankton biomass and total particulate carbon concentration. Unfortunately, c has proven difficult to quantify through remote sensing. Here, we introduce an innovative approach for estimating c using lidar depolarization measurements and diffuse attenuation coefficients from ocean color products or lidar measurements of Brillouin scattering. The new approach is based on a theoretical formula established from Monte Carlo simulations that links the depolarization ratio of sea water to the ratio of diffuse attenuation Kd and beam attenuation C (i.e., a multiple scattering factor). On July 17, 2014, the CALIPSO satellite was tilted 30Âdeg off-nadir for one nighttime orbit in order to minimize ocean surface backscatter and demonstrate the lidar ocean subsurface measurement concept from space. Depolarization ratios of ocean subsurface backscatter are measured accurately. Beam attenuation coefficients computed from the depolarization ratio measurements compare well with empirical estimates from ocean color measurements. We further verify the beam attenuation coefficient retrievals using aircraft-based high spectral resolution lidar (HSRL) data that are collocated with in-water optical measurements.

  13. Arctic carbon cycling

    NARCIS (Netherlands)

    Christensen, Torben R; Rysgaard, SØREN; Bendtsen, JØRGEN; Else, Brent; Glud, Ronnie N; van Huissteden, J.; Parmentier, F.J.W.; Sachs, Torsten; Vonk, J.E.

    2017-01-01

    The marine Arctic is considered a net carbon sink, with large regional differences in uptake rates. More regional modelling and observational studies are required to reduce the uncertainty among current estimates. Robust projections for how the Arctic Ocean carbon sink may evolve in the future are

  14. The effect of ocean acidification on carbon storage and sequestration in seagrass beds; a global and UK context.

    Science.gov (United States)

    Garrard, Samantha L; Beaumont, Nicola J

    2014-09-15

    Ocean acidification will have many negative consequences for marine organisms and ecosystems, leading to a decline in many ecosystem services provided by the marine environment. This study reviews the effect of ocean acidification (OA) on seagrasses, assessing how this may affect their capacity to sequester carbon in the future and providing an economic valuation of these changes. If ocean acidification leads to a significant increase in above- and below-ground biomass, the capacity of seagrass to sequester carbon will be significantly increased. The associated value of this increase in sequestration capacity is approximately £500 and 600 billion globally between 2010 and 2100. A proportionally similar increase in carbon sequestration value was found for the UK. This study highlights one of the few positive stories for ocean acidification and underlines that sustainable management of seagrasses is critical to avoid their continued degradation and loss of carbon sequestration capacity. Copyright © 2014 Elsevier Ltd. All rights reserved.

  15. Increase in acidifying water in the western Arctic Ocean

    Science.gov (United States)

    Qi, Di; Chen, Liqi; Chen, Baoshan; Gao, Zhongyong; Zhong, Wenli; Feely, Richard A.; Anderson, Leif G.; Sun, Heng; Chen, Jianfang; Chen, Min; Zhan, Liyang; Zhang, Yuanhui; Cai, Wei-Jun

    2017-02-01

    The uptake of anthropogenic CO2 by the ocean decreases seawater pH and carbonate mineral aragonite saturation state (Ωarag), a process known as Ocean Acidification (OA). This can be detrimental to marine organisms and ecosystems. The Arctic Ocean is particularly sensitive to climate change and aragonite is expected to become undersaturated (Ωarag Pacific Winter Water transport, driven by an anomalous circulation pattern and sea-ice retreat, is primarily responsible for the expansion, although local carbon recycling and anthropogenic CO2 uptake have also contributed. These results indicate more rapid acidification is occurring in the Arctic Ocean than the Pacific and Atlantic oceans, with the western Arctic Ocean the first open-ocean region with large-scale expansion of `acidified’ water directly observed in the upper water column.

  16. Multi-functionality Redefined with Colloidal Carotene Carbon Nanoparticles for Synchronized Chemical Imaging, Enriched Cellular Uptake and Therapy

    OpenAIRE

    Misra, Santosh K.; Mukherjee, Prabuddha; Chang, Huei-Huei; Tiwari, Saumya; Gryka, Mark; Bhargava, Rohit; Pan, Dipanjan

    2016-01-01

    Typically, multiplexing high nanoparticle uptake, imaging, and therapy requires careful integration of three different functions of a multiscale molecular-particle assembly. Here, we present a simpler approach to multiplexing by utilizing one component of the system for multiple functions. Specifically, we successfully synthesized and characterized colloidal carotene carbon nanoparticle (C3-NP), in which a single functional molecule served a threefold purpose. First, the presence of carotene ...

  17. A probabilistic assessment of calcium carbonate export and dissolution in the modern ocean

    Science.gov (United States)

    Battaglia, Gianna; Steinacher, Marco; Joos, Fortunat

    2016-05-01

    The marine cycle of calcium carbonate (CaCO3) is an important element of the carbon cycle and co-governs the distribution of carbon and alkalinity within the ocean. However, CaCO3 export fluxes and mechanisms governing CaCO3 dissolution are highly uncertain. We present an observationally constrained, probabilistic assessment of the global and regional CaCO3 budgets. Parameters governing pelagic CaCO3 export fluxes and dissolution rates are sampled using a Monte Carlo scheme to construct a 1000-member ensemble with the Bern3D ocean model. Ensemble results are constrained by comparing simulated and observation-based fields of excess dissolved calcium carbonate (TA*). The minerals calcite and aragonite are modelled explicitly and ocean-sediment fluxes are considered. For local dissolution rates, either a strong or a weak dependency on CaCO3 saturation is assumed. In addition, there is the option to have saturation-independent dissolution above the saturation horizon. The median (and 68 % confidence interval) of the constrained model ensemble for global biogenic CaCO3 export is 0.90 (0.72-1.05) Gt C yr-1, that is within the lower half of previously published estimates (0.4-1.8 Gt C yr-1). The spatial pattern of CaCO3 export is broadly consistent with earlier assessments. Export is large in the Southern Ocean, the tropical Indo-Pacific, the northern Pacific and relatively small in the Atlantic. The constrained results are robust across a range of diapycnal mixing coefficients and, thus, ocean circulation strengths. Modelled ocean circulation and transport timescales for the different set-ups were further evaluated with CFC11 and radiocarbon observations. Parameters and mechanisms governing dissolution are hardly constrained by either the TA* data or the current compilation of CaCO3 flux measurements such that model realisations with and without saturation-dependent dissolution achieve skill. We suggest applying saturation-independent dissolution rates in Earth system

  18. Effect of sulfite and fluoride on carbon dioxide uptake by mosses in the light

    Energy Technology Data Exchange (ETDEWEB)

    Inglis, F.; Hill, D.J.

    1974-01-01

    Four mosses, Bryum argenteum, Grimmia pulvinata, Hypnum cupressiforme and Tortula muralis were exposed to sulfite, and their uptake of radioactive bicarbonate measured. About 50% reduction in /sup 14/C uptake was caused by 0.01-0.1 mM sulfite. The effect of pH indicated that SO/sub 2/ (or H/sub 2/SO/sub 3/) was the active molecular species. Fluoride had little effect on /sup 14/C uptake.

  19. LOSCAR: Long-term Ocean-atmosphere-Sediment CArbon cycle Reservoir Model v2.0.4

    Directory of Open Access Journals (Sweden)

    R. E. Zeebe

    2012-01-01

    Full Text Available The LOSCAR model is designed to efficiently compute the partitioning of carbon between ocean, atmosphere, and sediments on time scales ranging from centuries to millions of years. While a variety of computationally inexpensive carbon cycle models are already available, many are missing a critical sediment component, which is indispensable for long-term integrations. One of LOSCAR's strengths is the coupling of ocean-atmosphere routines to a computationally efficient sediment module. This allows, for instance, adequate computation of CaCO3 dissolution, calcite compensation, and long-term carbon cycle fluxes, including weathering of carbonate and silicate rocks. The ocean component includes various biogeochemical tracers such as total carbon, alkalinity, phosphate, oxygen, and stable carbon isotopes. LOSCAR's configuration of ocean geometry is flexible and allows for easy switching between modern and paleo-versions. We have previously published applications of the model tackling future projections of ocean chemistry and weathering, pCO2 sensitivity to carbon cycle perturbations throughout the Cenozoic, and carbon/calcium cycling during the Paleocene-Eocene Thermal Maximum. The focus of the present contribution is the detailed description of the model including numerical architecture, processes and parameterizations, tuning, and examples of input and output. Typical CPU integration times of LOSCAR are of order seconds for several thousand model years on current standard desktop machines. The LOSCAR source code in C can be obtained from the author by sending a request to loscar.model@gmail.com.

  20. Changes in ocean circulation and carbon storage are decoupled from air-sea CO2 fluxes

    OpenAIRE

    A. Gnanadesikan; I. Marinov

    2010-01-01

    The spatial distribution of the air-sea flux of carbon dioxide is a poor indicator of the underlying ocean circulation and of ocean carbon storage. The weak dependence on circulation arises because mixing-driven changes in solubility-driven and biologically-driven air-sea fluxes largely cancel out. This cancellation occurs because mixing driven increases in the poleward residual mean circulation results in more transport of both remineralized nutrients and heat from low to high latitudes. By ...

  1. Modeling long-term carbon residue in the ocean-atmosphere system following large CO2 emissions

    Science.gov (United States)

    Towles, N. J.; Olson, P.; Gnanadesikan, A.

    2013-12-01

    We use the LOSCAR carbon cycle model (Zeebe et al., 2009; Zeebe, 2012) to calculate the residual carbon in the ocean and atmosphere following large CO2 emissions. We consider the system response to CO2 emissions ranging from 100 to 20000 PgC, and emission durations from 100 yr to 100 kyr, subject to a wide range of system parameters such as the strengths of silicate weathering and the oceanic biological carbon pump. We define the carbon gain factor as the ratio of residual carbon in the ocean-atmosphere to the total emitted carbon. For moderate sized emissions shorter than about 50 kyr, we find that the carbon gain factor grows during the emission and peaks at about 1.7, primarily due to the erosion of carbonate marine sediments. In contrast, for longer emissions, the carbon gain factor peaks at a smaller value, and for very large emissions (more than 5000 PgC), the gain factor decreases with emission size due to carbonate sediment exhaustion. This gain factor is sensitive to model parameters such as low latitude efficiency of the biological pump. The timescale for removal of the residual carbon (reducing the carbon gain factor to zero) depends strongly on the assumed sensitivity of silicate weathering to atmospheric pCO2, and ranges from less than one million years to several million years.

  2. Input of particulate organic and dissolved inorganic carbon from the Amazon to the Atlantic Ocean

    Science.gov (United States)

    Druffel, E. R. M.; Bauer, J. E.; Griffin, S.

    2005-03-01

    We report concentrations and isotope measurements (radiocarbon and stable carbon) of dissolved inorganic carbon (DIC) and suspended particulate organic carbon (POC) in waters collected from the mouth of the Amazon River and the North Brazil Current. Samples were collected in November 1991, when the Amazon hydrograph was at its annual minimum and the North Brazil Current had retroflected into the equatorial North Atlantic. The DIC Δ14C results revealed postbomb carbon in river and ocean waters, with slightly higher values at the river mouth. The low DIC δ13C signature of the river end-member (-11‰) demonstrates that about half of the DIC originated from the remineralization of terrestrially derived organic matter. A linear relationship between DIC and salinity indicates that DIC was mixed nearly conservatively in the transition zone from the river mouth to the open ocean, though there was a small amount (≤10%) of organic matter remineralization in the mesohaline region. The POC Δ14C values in the river mouth were markedly lower than those values from the western Amazon region (Hedges et al., 1986). We conclude that the dominant source of POC near the river mouth and in the inner Amazon plume during November 1991 was aged, resuspended material of significant terrestrial character derived from shelf sediments, while the outer plume contained mainly marine-derived POC.

  3. The potential of 230Th for detection of ocean acidification impacts on pelagic carbonate production

    Directory of Open Access Journals (Sweden)

    C. Heinze

    2018-06-01

    Full Text Available Concentrations of dissolved 230Th in the ocean water column increase with depth due to scavenging and downward particle flux. Due to the 230Th scavenging process, any change in the calcium carbonate (CaCO3 fraction of the marine particle flux due to changes in biological CaCO3 hard-shell production as a consequence of progressing ocean acidification would be reflected in the dissolved 230Th activity. Our prognostic simulations with a biogeochemical ocean general circulation model using different scenarios for the reduction of CaCO3 production under ocean acidification and different greenhouse gas emission scenarios – the Representative Concentration Pathways (RCPs 8.5 to 2.6 – reveal the potential for deep 230Th measurements to detect reduced CaCO3 production at the sea surface. The time of emergence of an acidification-induced signal on dissolved 230Th is of the same order of magnitude as for alkalinity measurements. Interannual and decadal variability in factors other than a reduction in CaCO3 hard-shell production may mask the ocean-acidification-induced signal in dissolved 230Th and make detection of the pure CaCO3-induced signal more difficult so that only really strong changes in marine CaCO3 export would be unambiguously identifiable soon. Nevertheless, the impacts of changes in CaCO3 export production on marine 230Th are stronger than those for changes in POC (particulate organic carbon or clay fluxes.

  4. Exploring the Disappearing Ocean Micro Plastic Mystery: New Insights from Dissolved Organic Carbon photo production

    Science.gov (United States)

    Zhu, L.; Zhao, S.; Li, D.; Stubbins, A.

    2017-12-01

    Emerging as a novel planetary threat, plastic waste, dominated by millimeter-sized plastic (microplastic), is omnipresent in the oceans, posing broad environmental threats. However, only 1% of the microplastic waste exported from the land is found in the ocean. Most of the lost fraction is in the form of microplastics. The fate of these buoyant plastic fragments is a fundamental gap in our understanding of the fate and impact of plastics in marine ecosystems. To date, an effective sink for the lost microplastics has not been found. In this study, dissolved organic carbon (DOC) photo-production from the three dominant forms of ocean microplastics was assessed. These plastics were: 1) Polyethylene (PE) both for postconsumer samples and pure standard samples; 2) polypropylene (PP); and, expanded polystyrene (EPS). In addition, a Neustonic microplastic samples from the North Pacific Gyre were irradiated. These real-world samples were dominated by PE ( 80%). All samples were placed in seawater, in quartz flasks, and irradiated in a solar simulator for 2 months. During irradiation, DOC photo-production from PP, EPS, and the PE standard was exponential, while DOC photo-production from postconsumer PE and the Neustonic samples was linear. Scanning electron microscopy indicated surface ablation and micro-fragmentation during the irradiation of the three plastics that showed exponential DOC production (PP, EPS and standard PE), suggesting the increase in photo-reactivity of these plastics was a result of an increase in their surface to volume ratios and therefore their per-unit mass light exposure. Based on DOC production, the half-life of the microplastics ranged from 0.26 years for EPS to 86 years for PE, suggesting sunlight is a major removal term for buoyant oceanic microplastics. With respect to the broader carbon cycle, we conservatively estimate that plastic photodegradation releases 6 to 17 thousand metric tons of radiocarbon dead DOC to the surface ocean each year.

  5. Evolution of organic carbon burial in the Global Ocean during the Neogene

    Science.gov (United States)

    LI, Z.; Zhang, Y.

    2017-12-01

    Although only a small fraction of the organic carbon (OC) that rains from surface waters is eventually buried in the sediments, it is a process that controls the organic sub-cycle of the long-term carbon cycle, and the key for atmospheric O2, CO2 and nutrient cycling. Here we constrain the spatiotemporal variability of OC burial by quantifying the total organic carbon (TOC) mass accumulation rate (MAR) over the Neogene (23.0-2.6 Ma) by compiling the TOC, age model and sediment density data from sites retrieved by the Deep Sea Drilling Program, Ocean Drilling Program, and Integrated Ocean Drilling Program. We screened all available sites which yielded 80 sites with adequate data quality, covering all major ocean basins and sedimentary depositional environments. All age models are updated to the GTS 2012 timescale so the TOC MAR records from different sites are comparable. Preliminary results show a clear early Miocene peak of OC burial in many sites related to high sediment flux which might reflect the orogenic uplift and/or glacier erosion. Places that receive high influx of terrigenous inputs become "hotspots" for Neogene burial of OC. At "open ocean" sites, OC burial seems to be more impacted by marine productivity changes, with a pronounced increase during the middle Miocene "Monterey Formation" and late Miocene - early Pliocene "Biogenic Bloom". Upon the completion of the data collection, we will further explore the regional and global OC burial in the context of tectonic uplift, climate change and the evolution of primary producers and consumers during the last 23 million years of Earth history.

  6. Role of regression model selection and station distribution on the estimation of oceanic anthropogenic carbon change by eMLR

    Directory of Open Access Journals (Sweden)

    Y. Plancherel

    2013-07-01

    Full Text Available Quantifying oceanic anthropogenic carbon uptake by monitoring interior dissolved inorganic carbon (DIC concentrations is complicated by the influence of natural variability. The "eMLR method" aims to address this issue by using empirical regression fits of the data instead of the data themselves, inferring the change in anthropogenic carbon in time by difference between predictions generated by the regressions at each time. The advantages of the method are that it provides in principle a means to filter out natural variability, which theoretically becomes the regression residuals, and a way to deal with sparsely and unevenly distributed data. The degree to which these advantages are realized in practice is unclear, however. The ability of the eMLR method to recover the anthropogenic carbon signal is tested here using a global circulation and biogeochemistry model in which the true signal is known. Results show that regression model selection is particularly important when the observational network changes in time. When the observational network is fixed, the likelihood that co-located systematic misfits between the empirical model and the underlying, yet unknown, true model cancel is greater, improving eMLR results. Changing the observational network modifies how the spatio-temporal variance pattern is captured by the respective datasets, resulting in empirical models that are dynamically or regionally inconsistent, leading to systematic errors. In consequence, the use of regression formulae that change in time to represent systematically best-fit models at all times does not guarantee the best estimates of anthropogenic carbon change if the spatial distributions of the stations emphasize hydrographic features differently in time. Other factors, such as a balanced and representative station coverage, vertical continuity of the regression formulae consistent with the hydrographic context and resiliency of the spatial distribution of the residual

  7. Quantifying and predicting historical and future patterns of carbon fluxes from the North American Continent to Ocean

    Science.gov (United States)

    Tian, H.; Zhang, B.; Xu, R.; Yang, J.; Yao, Y.; Pan, S.; Lohrenz, S. E.; Cai, W. J.; He, R.; Najjar, R. G.; Friedrichs, M. A. M.; Hofmann, E. E.

    2017-12-01

    Carbon export through river channels to coastal waters is a fundamental component of the global carbon cycle. Changes in the terrestrial environment, both natural (e.g., climatic change, enriched CO2 concentration, and elevated ozone concentration) and anthropogenic (e.g, deforestation, cropland expansion, and urbanization) have greatly altered carbon production, stocks, decomposition, movement and export from land to river and ocean systems. However, the magnitude and spatiotemporal patterns of lateral carbon fluxes from land to oceans and the underlying mechanisms responsible for these fluxes remain far from certain. Here we applied a process-based land model with explicit representation of carbon processes in stream and rivers (Dynamic Land Ecosystem Model: DLEM 2.0) to examine how changes in climate, land use, atmospheric CO2, and nitrogen deposition have affected the carbon fluxes from North American continent to Ocean during 1980-2015. Our simulated results indicated that terrestrial carbon export shows substantially spatial and temporal variability. Of the five sub-regions (Arctic coast, Pacific coast, Gulf of Mexico, Atlantic coast, and Great lakes), the Arctic sub-region provides the highest DOC flux, whereas the Gulf of Mexico sub-region provided the highest DIC flux. However, terrestrial carbon export to the arctic oceans showed increasing trends for both DOC and DIC, whereas DOC and DIC export to the Gulf of Mexico decreased in the recent decades. Future pattern of riverine carbon fluxes would be largely dependent on the climate change and land use scenarios.

  8. Functional group diversity is key to Southern Ocean benthic carbon pathways.

    Directory of Open Access Journals (Sweden)

    David K A Barnes

    Full Text Available High latitude benthos are globally important in terms of accumulation and storage of ocean carbon, and the feedback this is likely to have on regional warming. Understanding this ecosystem service is important but difficult because of complex taxonomic diversity, history and geography of benthic biomass. Using South Georgia as a model location (where the history and geography of benthic biology is relatively well studied we investigated whether the composition of functional groups were critical to benthic accumulation, immobilization and burial pathway to sequestration-and also aid their study through simplification of identification. We reclassified [1], [2] morphotype and carbon mass data to 13 functional groups, for each sample of 32 sites around the South Georgia continental shelf. We investigated the influence on carbon accumulation, immobilization and sequestration estimate by multiple factors including the compositions of functional groups. Functional groups showed high diversity within and between sites, and within and between habitat types. Carbon storage was not linked to a functional group in particular but accumulation and immobilization increased with the number of functional groups present and the presence of hard substrata. Functional groups were also important to carbon burial rate, which increased with the presence of mixed (hard and soft substrata. Functional groups showed high surrogacy for taxonomic composition and were useful for examining contrasting habitat categorization. Functional groups not only aid marine carbon storage investigation by reducing time and the need for team size and speciality, but also important to benthic carbon pathways per se. There is a distinct geography to seabed carbon storage; seabed boulder-fields are hotspots of carbon accumulation and immobilization, whilst the interface between such boulder-fields and sediments are key places for burial and sequestration.

  9. Surface water carbon dioxide in the southwest Indian sector of the Southern Ocean

    International Nuclear Information System (INIS)

    Metzl, N.; Brunet, C.; Poisson, A.

    1991-01-01

    Measurements of partial pressure of carbon dioxide (pCO 2 ), total dissolved inorganic carbon (TCO 2 ), total alkalinity (TA) and chlorophyll a (Chl a) have been made in surface water in the southwestern Indian sector of the Southern Ocean (20-85 degE) in the austral summer (INDIVAT V cruise, January-February 1987). Between Antarctica and Africa, pCO 2 distribution was linked to the oceanic frontal zones and Chl a variations. The pCO 2 spatial structure was very close to that explored in summer 1967 in the same region but the pCO 2 differences between the ocean and the atmosphere were smaller in 1987 than 20 years ago. At all latitudes strongly contrasting surface pCO 2 characteristics were found between eastern (around 80 degE) and western (around 25 degE) regions; CO 2 sources were mainly in the west and CO 2 sinks in the east. South of 60 degS, the contrast could be due to biological activity. Between 60 degS and the Antarctic Polar Front, intensification of upwelling might be responsible for the higher pC) 2 values in the west.37 refs.; 4 figs

  10. Evolutionary and geologic consequences of organic carbon fixing in the primitive anoxic ocean

    Science.gov (United States)

    Berry, W. B. N.; Wilde, P.

    1983-03-01

    Steps leading to development of the modern photic-based marine food web are postulated as the result of modifications of the environment, enhanced by the activity of Archean sulfur chemoautotrophs. Such organisms (Anoxium) evolved in an anoxic ocean prior to 3.9 × 109 yr ago at Archean analogs of modern oceanic hydrothermal vents. At this time geothermal energy was more readily available to organisms than photic energy, given atmospheric conditions at the surface similar to Venus, where intensity is low and only middle and red visible wavelengths penetrate the cloudy CO2-rich atmosphere. Competition for the reduced sulfur developed due to oxidation and loss of sulfur to sediments. Consequently, evolutionary advantage shifted to Anoxium isolates that could use alternate energy sources such as light to supplement the diminished supplies of reduced sulfur. Initially, photo-sulfur organisms evolved similar to modern purple bacteria that absorb in the red visible spectra. Subsequent carbon fixing and oxidation improved both the quantity and range of light reaching the ocean surface. This permitted absorption in the blue visible range so that water splitting was now feasible, releasing free oxygen and accelerating oxidation. Eventually, reducing environments became restricted, completing the shift in the principal marine carbon-fixing activity from anoxic chemoautotrophic to aerobic photosynthetic organisms.

  11. Carbon cycle, chemical erosion of continents and transfers to the oceans

    International Nuclear Information System (INIS)

    Amiotte Suchet, P.

    1995-01-01

    This study tries to define the processes that control the CO 2 consumption due to the chemical erosion of continents, to appreciate the spatial-temporal fluxes of consumed CO 2 , and to estimate the transfers of dissolved mineral carbon from the continents to the oceans. Complementary approaches using different scales of time and space are necessary to study all these processes. Chemical alteration of minerals from continental rocks is due to the carbonic acid indirectly produced by atmospheric CO 2 via the photosynthesis and the degradation of organic matter in soils. The transfer of dissolved CO 2 towards the oceans is done by the drainage waters of the river basins. Continental erosion develops at the interfaces of the biosphere, atmosphere and ocean reservoirs and is controlled by numerous geological, hydro-climatical, biological and anthropic factors. Seasonal variations of CO 2 consumption has been studied for the Garonne (France), Congo and Ubangui basins to determine the mechanisms that control this consumption. A predictive model has been developed to simulate the consumed CO 2 fluxes on continental surfaces for which the spatial distribution of lithology and drainage is known. This model has been validated using available data from the Garonne (France), Congo and Amazone basins. (J.S.). 272 refs., 78 figs., 41 tabs., 1 annexe

  12. A neural network-based estimate of the seasonal to inter-annual variability of the Atlantic Ocean carbon sink

    DEFF Research Database (Denmark)

    Landschützer, P.; Gruber, N.; Bakker, D.C.E.

    2013-01-01

    The Atlantic Ocean is one of the most important sinks for atmospheric carbon dioxide (CO2), but this sink is known to vary substantially in time. Here we use surface ocean CO2 observations to estimate this sink and the temporal variability from 1998 to 2007 in the Atlantic Ocean. We benefit from ......, leading to a substantial trend toward a stronger CO2 sink for the entire South Atlantic (–0.14 Pg C yr–1 decade–1). The Atlantic carbon sink varies relatively little on inter-annual time-scales (±0.04 Pg C yr–1; 1σ)......The Atlantic Ocean is one of the most important sinks for atmospheric carbon dioxide (CO2), but this sink is known to vary substantially in time. Here we use surface ocean CO2 observations to estimate this sink and the temporal variability from 1998 to 2007 in the Atlantic Ocean. We benefit from (i...... poleward of 40° N, but many other parts of the North Atlantic increased more slowly, resulting in a barely changing Atlantic carbon sink north of the equator (–0.007 Pg C yr–1 decade–1). Surface ocean pCO2 was also increasing less than that of the atmosphere over most of the Atlantic south of the equator...

  13. Climate change feedbacks on future oceanic acidification

    International Nuclear Information System (INIS)

    McNeil, Ben I.; Matear, Richard J.

    2007-01-01

    Oceanic anthropogenic CO 2 uptake will decrease both the pH and the aragonite saturation state (Oarag) of seawater leading to an oceanic acidification. However, the factors controlling future changes in pH and Oarag are independent and will respond differently to oceanic climate change feedbacks such as ocean warming, circulation and biological changes. We examine the sensitivity of these two CO 2 -related parameters to climate change feedbacks within a coupled atmosphere-ocean model. The ocean warming feedback was found to dominate the climate change responses in the surface ocean. Although surface pH is projected to decrease relatively uniformly by about 0.3 by the year 2100, we find pH to be insensitive to climate change feedbacks, whereas Oarag is buffered by ∼15%. Ocean carbonate chemistry creates a situation whereby the direct pH changes due to ocean warming are almost cancelled by the pH changes associated with dissolved inorganic carbon concentrations changes via a reduction in CO 2 solubility from ocean warming. We show that the small climate change feedback on future surface ocean pH is independent to the amount of ocean warming. Our analysis therefore implies that future projections of surface ocean acidification only need to consider future atmospheric CO 2 levels, not climate change induced modifications in the ocean

  14. Impact of oceanic processes on the carbon cycle during the last termination

    Science.gov (United States)

    Bouttes, N.; Paillard, D.; Roche, D. M.; Waelbroeck, C.; Kageyama, M.; Lourantou, A.; Michel, E.; Bopp, L.

    2012-01-01

    During the last termination (from ~18 000 years ago to ~9000 years ago), the climate significantly warmed and the ice sheets melted. Simultaneously, atmospheric CO2 increased from ~190 ppm to ~260 ppm. Although this CO2 rise plays an important role in the deglacial warming, the reasons for its evolution are difficult to explain. Only box models have been used to run transient simulations of this carbon cycle transition, but by forcing the model with data constrained scenarios of the evolution of temperature, sea level, sea ice, NADW formation, Southern Ocean vertical mixing and biological carbon pump. More complex models (including GCMs) have investigated some of these mechanisms but they have only been used to try and explain LGM versus present day steady-state climates. In this study we use a coupled climate-carbon model of intermediate complexity to explore the role of three oceanic processes in transient simulations: the sinking of brines, stratification-dependent diffusion and iron fertilization. Carbonate compensation is accounted for in these simulations. We show that neither iron fertilization nor the sinking of brines alone can account for the evolution of CO2, and that only the combination of the sinking of brines and interactive diffusion can simultaneously simulate the increase in deep Southern Ocean δ13C. The scenario that agrees best with the data takes into account all mechanisms and favours a rapid cessation of the sinking of brines around 18 000 years ago, when the Antarctic ice sheet extent was at its maximum. In this scenario, we make the hypothesis that sea ice formation was then shifted to the open ocean where the salty water is quickly mixed with fresher water, which prevents deep sinking of salty water and therefore breaks down the deep stratification and releases carbon from the abyss. Based on this scenario, it is possible to simulate both the amplitude and timing of the long-term CO2 increase during the last termination in agreement with

  15. Rethinking CCD's Significance in Estimating Late Neogene Whole Ocean Carbonate Budget

    Science.gov (United States)

    Si, W.; Rosenthal, Y.

    2017-12-01

    The global averaged calcite compensation depth (CCD) record is conventionally used to reconstruct two correlatable parameters of the carbonate system - the alkalinity budget of the ocean and/or the saturation state of the ocean. Accordingly, the available CCD reconstructions have been interpreted to suggest either relative stable (Pearson and Palmer, 2000) or increased alkalinity of the ocean over the past 15 Ma (Tyrrell and Zeebe, 2004; Pälike et al., 2012). However, CCD alone is insufficient to constrain the carbonate system because the weathering flux of alkalinity into the ocean is not only balanced by CaCO3 dissolution on the seafloor but also by the biologic production in the euphotic zone and, the CCD records cannot be readily interpreted as changes in either process. Here, we present evidence of the co-evolution of surface CaCO3 production and deepsea dissolution through the late Neogene. By examining separately the mass accumulation rates (MAR) of coccoliths, planktonic foraminifera, and quantifying dissolution (using a proxy revised from Broecker et al., 1999) in seventeen deepsea cores from multiple depth-transects, we find that 1) MAR of dissolution-resistant coccoliths was substantially higher in the mid Miocene and declining on a global scale towards the present; 2) unlike coccoliths, MAR of planktonic foraminifera, shows no apparent secular trend through that time; 3) the revised dissolution index, shows significantly improved preservation of planktonic foraminiferal shells over that time, particularly at intermediate water depth and exhibits close association between changes in preservation with key climatic events. Our new records have two immediate implications. First, the substantially weakened pelagic biogenic carbonate production from mid Miocene to present alone could account for the improved preservation of deepsea carbonates without calling for a scenario of increased weathering input. Second, with the constrain of global averaged CCD

  16. Fast reconnaissance of carbonate dissolution based on the size distribution of calcareous ooze on Walvis Ridge, SE Atlantic Ocean.

    NARCIS (Netherlands)

    Stuut, J.-B. W.; Prins, M.A.; Jansen, J.H.F.

    2002-01-01

    We present a new index of carbonate fragmentation based on the size distribution of bulk sediments in core MD962094 from Walvis Ridge (SE Atlantic Ocean). The carbonate fragmentation index is constructed by taking a ratio of the two coarsest fractions in the grain size distributions of the bulk

  17. Hydrothermal Fe cycling and deep ocean organic carbon scavenging: Model-based evidence for significant POC supply to seafloor sediments

    Digital Repository Service at National Institute of Oceanography (India)

    German, C.R.; Legendre, L.L.; Sander, S.G.;; Niquil, N.; Luther-III, G.W.; LokaBharathi, P.A.; Han, X.; LeBris, N.

    by more than ~10% over background values, what the model does indicate is that scavenging of carbon in association with Fe-rich hydrothermal plume particles should play a significant role in the delivery of particulate organic carbon to deep ocean...

  18. Atmospheric CO2 Observations Reveal Strong Correlation Between Regional Net Biospheric Carbon Uptake and Solar-Induced Chlorophyll Fluorescence

    Science.gov (United States)

    Shiga, Yoichi P.; Tadić, Jovan M.; Qiu, Xuemei; Yadav, Vineet; Andrews, Arlyn E.; Berry, Joseph A.; Michalak, Anna M.

    2018-01-01

    Recent studies have shown the promise of remotely sensed solar-induced chlorophyll fluorescence (SIF) in informing terrestrial carbon exchange, but analyses have been limited to either plot level ( 1 km2) or hemispheric/global ( 108 km2) scales due to the lack of a direct measure of carbon exchange at intermediate scales. Here we use a network of atmospheric CO2 observations over North America to explore the value of SIF for informing net ecosystem exchange (NEE) at regional scales. We find that SIF explains space-time NEE patterns at regional ( 100 km2) scales better than a variety of other vegetation and climate indicators. We further show that incorporating SIF into an atmospheric inversion leads to a spatial redistribution of NEE estimates over North America, with more uptake attributed to agricultural regions and less to needleleaf forests. Our results highlight the synergy of ground-based and spaceborne carbon cycle observations.

  19. Spectroscopic and Microscopic Characterization of Contaminant Uptake and Retention by Carbonates in the Soil and Vadose Zone

    International Nuclear Information System (INIS)

    Reeder, Richard J.; Fisher, Nicholas S.; Hess, Wayne P.; Beck, Kenneth M.

    2003-01-01

    The research focus of this previous EMSP grant was assessment of the role that carbonate minerals play in the uptake and sequestration of metal and radionuclide contaminants in soils and the vadose zone for conditions relevant to the Hanford Site and other sites in the DOE Complex. The project was a collaboration among researchers at SUNY-Stony Brook and EMSL/PNNL. Carbonates, particularly calcite, are present in the Hanford subsurface as grain coatings, disseminated particles, and dense caliche layers. Calcite is also predicted to be forming beneath leaking tanks. A range of metal and radionuclide species that pose risks at Hanford and other DOE sites were considered, including U(VI), Cr(CV), Cs, Pb(II), and selected lanthanides (as models for trivalent actinides). Batch sorption and co-precipitation experiments of these metals with pre-equilibrated calcite and selected uptake experiments on natural caliche formed the basis to determine the mechanisms of metal/radionuclide binding and to assess the effect on the stability of the sorbed species and the potential for remobilization. Our results provide ne information that can benefit DOE clean-up methodology and potentially provide new approaches for uptake of selected heavy metals

  20. Effect of aspect ratio on the uptake and toxicity of hydroxylated-multi walled carbon nanotubes in the nematode,

    Directory of Open Access Journals (Sweden)

    Hyun-Jeong Eom

    2015-03-01

    Full Text Available Objectives In this study, the effect of tube length and outer diameter (OD size of hydroxylated-multi walled carbon nanotubes (OH-MWCNTs on their uptake and toxicity was investigated in the nematode Caenorhabditis elegans using a functional mutant analysis. Methods The physicochemical properties of three different OH-MWCNTs were characterized. Uptake and toxicity were subsequently investigated on C. elegans exposed to MWCNTs with different ODs and tube lengths. Results The results of mutant analysis suggest that ingestion is the main route of MWCNTs uptake. We found that OH-MWCNTs with smaller ODs were more toxic than those with larger ODs, and OH-MWCNTs with shorter tube lengths were more toxic than longer counterparts to C. elegans. Conclusions Overall the results suggest the aspect ratio affects the toxicity of MWCNTs in C. elegans. Further thorough study on the relationship between physicochemical properties and toxicity needs to be conducted for more comprehensive understanding of the uptake and toxicity of MWCNTs.

  1. Variation pattern of particulate organic carbon and nitrogen in oceans and inland waters

    Science.gov (United States)

    Huang, Changchun; Jiang, Quanliang; Yao, Ling; Yang, Hao; Lin, Chen; Huang, Tao; Zhu, A.-Xing; Zhang, Yimin

    2018-03-01

    We examined the relationship between, and variations in, particulate organic carbon (POC) and particulate organic nitrogen (PON) based on previously acquired ocean and inland water data. The latitudinal dependency of POC / PON is significant between 20 and 90° N but weak in low-latitude areas and in the Southern Hemisphere. The mean values of POC / PON in the Southern Hemisphere and Northern Hemisphere were 7.40 ± 3.83 and 7.80 ± 3.92, respectively. High values of POC / PON appeared between 80-90 (12.2 ± 7.5) and 70-80° N (9.4 ± 6.4), while relatively low POC / PON was found from 20 (6.6 ± 2.8) to 40° N (6.7 ± 2.7). The latitudinal variation of POC / PON in the Northern Hemisphere is much stronger than in the Southern Hemisphere due to the influence of more terrestrial organic matter. Higher POC and PON could be expected in coastal waters. POC / PON growth ranged from 6.89 ± 2.38 to 7.59 ± 4.22 in the Northern Hemisphere, with an increasing rate of 0.0024 km from the coastal to open ocean. Variations of POC / PON in lake water also showed a similar latitude-variation tendency of POC / PON with ocean water but were significantly regulated by the lakes' morphology, trophic state and climate. Small lakes and high-latitude lakes prefer relatively high POC / PON, and large lakes and low-latitude lakes tend to prefer low POC / PON. The coupling relationship between POC and PON in oceans is much stronger than in inland waters. Variations in POC, PON and POC / PON in inland waters should receive more attention due to the implications of these values for the global carbon and nitrogen cycles and the indeterminacy of the relationship between POC and PON.

  2. Temperature evolution and the oxygen isotope composition of Phanerozoic oceans from carbonate clumped isotope thermometry

    Science.gov (United States)

    Henkes, Gregory A.; Passey, Benjamin H.; Grossman, Ethan L.; Shenton, Brock J.; Yancey, Thomas E.; Pérez-Huerta, Alberto

    2018-05-01

    Surface temperature is among the most important parameters describing planetary climate and habitability, and yet there remains considerable debate about the temperature evolution of the Earth's oceans during the Phanerozoic Eon (541 million years ago to present), the time during which complex metazoan life radiated on Earth. Here we critically assess the emerging record of Phanerozoic ocean temperatures based on carbonate clumped isotope thermometry of fossil brachiopod and mollusk shells, and we present new data that fill important gaps in the Late Paleozoic record. We evaluate and reject the hypothesis that solid-state reordering of 13C-18O bonds has destroyed the primary clumped isotope temperature signal of most fossils during sedimentary burial at elevated temperatures. The resulting Phanerozoic record, which shows a general coupling between tropical seawater temperatures and atmospheric carbon dioxide (CO2) levels since the Paleozoic, indicates that tropical temperatures during the icehouse climate of the Carboniferous period were broadly similar to present (∼25-30 °C), and suggests that benthic metazoans were able to thrive at temperatures of 35-40 °C during intervals of the early and possibly the latest Paleozoic when CO2 levels were likely 5-10× higher than present-day values. Equally important, there is no resolvable trend in seawater oxygen isotope ratios (δ18 O) over the past ∼500 million years, indicating that the average temperature of oxygen exchange between seawater and the oceanic crust has been high (∼270 °C) since at least the early Paleozoic, which points to mid-ocean ridges as the dominant locus of water-rock interaction over the past half-billion years.

  3. Benthic metabolic feedbacks to carbonate chemistry on coral reefs:implications for ocean acidification

    Science.gov (United States)

    Price, N.; Rohwer, F. L.; Stuart, S. A.; Andersson, A.; Smith, J.

    2012-12-01

    The metabolic activity of resident organisms can cause spatio-temporal variability in carbonate chemistry within the benthic boundary layer, and thus potentially buffer the global impacts of ocean acidification. But, little is known about the capacity for particular species assemblages to contribute to natural daily variability in carbonate chemistry. We encapsulated replicate areas (~3m2) of reef across six Northern Line Islands in the central Pacific for 24 hrs to quantify feedbacks to carbonate chemistry within the benthic boundary layer from community metabolism. Underneath each 'tent', we quantified relative abundance and biomass of each species of corals and algae. We coupled high temporal resolution time series data on the natural diurnal variability in pH, dissolved oxygen, salinity, and temperature (using autonomous sensors) with resident organisms' net community calcification and productivity rates (using change in total dissolved carbon and total alkalinity over time) to examine feedbacks from reef metabolism to boundary layer carbonate chemistry. These reefs experienced large ranges in pH (> 0.2 amplitude) each day, similar to the magnitude of 'acidification' expected over the next century. Daily benthic pH, pCO2, and aragonite saturation state (Ωaragonite) were contrasted with seasonal threshold values estimated from open ocean climatological data extrapolated at each island to determine relative inter-island feedbacks. Diurnal amplitude in pH, pCO2, and Ωaragonite at each island was dependent upon the resident species assemblage of the benthos and was particularly reliant upon the biomass, productivity, and calcification rate of Halimeda. Net primary productivity of fleshy algae (algal turfs and Lobophora spp.) predominated on degraded, inhabited islands where net community calcification was negligible. In contrast, the chemistry over reefs on 'pristine', uninhabited islands was driven largely by net calcification of calcareous algae and stony

  4. Carbon Transformations and Source - Sink Dynamics along a River, Marsh, Estuary, Ocean Continuum

    Science.gov (United States)

    Anderson, I. C.; Crosswell, J.; Czapla, K.; Van Dam, B.

    2017-12-01

    Estuaries, the transition zone between land and the coastal ocean, are highly dynamic systems in which carbon sourced from watersheds, marshes, atmosphere, and ocean may be transformed, sequestered, or exported. The net fate of carbon in estuaries, governed by the interactions of biotic and physical drivers varying on spatial and temporal scales, is currently uncertain because of limited observational data. In this study, conducted in a temperate, microtidal, and shallow North Carolina USA estuary, carbon exchanges via river, tributary, and fringing salt marsh, air-water fluxes, sediment C accumulation, and metabolism were monitored over two-years, with sharply different amounts of rainfall. Air-water CO2 fluxes and metabolic variables were simultaneously measured in channel and shoal by conducting high-resolution surveys at dawn, dusk and the following dawn. Marsh CO2 exchanges, sediment C inputs, and lateral exports of DIC and DOC were also measured. Carbon flows between estuary regions and export to the coastal ocean were calculated by quantifying residual transport of DIC and TOC down-estuary as flows were modified by sources, sinks and internal transformations. Variation in metabolic rates, CO2, TOC and DIC exchanges were large when determined for short time and limited spatial scales. However, when scaled to annual and whole estuarine scales, variation tended to decrease because of counteracting metabolic rates and fluxes between channel and shoal or between seasons. Although overall salt marshes accumulated OC, they were a negligible source of DIC and DOC to the estuary, and net inputs of C to the marsh were mainly derived from sediment OC. These results, as observed in other observational studies of estuaries, show that riverine input, light, temperature and metabolism are major controls on carbon cycling. Comparison of our results with other types of estuaries varying in depth, latitude, and nutrification demonstrates large discrepancies underscoring the

  5. Peak season plant activity shift towards spring is reflected by increasing carbon uptake by extratropical ecosystems.

    Science.gov (United States)

    Gonsamo, Alemu; Chen, Jing M; Ooi, Ying W

    2018-05-01

    Climate change is lengthening the growing season of the Northern Hemisphere extratropical terrestrial ecosystems, but little is known regarding the timing and dynamics of the peak season of plant activity. Here, we use 34-year satellite normalized difference vegetation index (NDVI) observations and atmospheric CO 2 concentration and δ 13 C isotope measurements at Point Barrow (Alaska, USA, 71°N) to study the dynamics of the peak of season (POS) of plant activity. Averaged across extratropical (>23°N) non-evergreen-dominated pixels, NDVI data show that the POS has advanced by 1.2 ± 0.6 days per decade in response to the spring-ward shifts of the start (1.0 ± 0.8 days per decade) and end (1.5 ± 1.0 days per decade) of peak activity, and the earlier onset of the start of growing season (1.4 ± 0.8 days per decade), while POS maximum NDVI value increased by 7.8 ± 1.8% for 1982-2015. Similarly, the peak day of carbon uptake, based on calculations from atmospheric CO 2 concentration and δ 13 C data, is advancing by 2.5 ± 2.6 and 4.3 ± 2.9 days per decade, respectively. POS maximum NDVI value shows strong negative relationships (p POS days. Given that the maximum solar irradiance and day length occur before the average POS day, the earlier occurrence of peak plant activity results in increased plant productivity. Both the advancing POS day and increasing POS vegetation greenness are consistent with the shifting peak productivity towards spring and the increasing annual maximum values of gross and net ecosystem productivity simulated by coupled Earth system models. Our results further indicate that the decline in autumn NDVI is contributing the most to the overall browning of the northern high latitudes (>50°N) since 2011. The spring-ward shift of peak season plant activity is expected to disrupt the synchrony of biotic interaction and exert strong biophysical feedbacks on climate by modifying the surface albedo and energy budget. © 2017

  6. Heterotrophic denitrification vs. autotrophic anammox – quantifying collateral effects on the oceanic carbon cycle

    Directory of Open Access Journals (Sweden)

    W. Koeve

    2010-08-01

    Full Text Available The conversion of fixed nitrogen to N2 in suboxic waters is estimated to contribute roughly a third to total oceanic losses of fixed nitrogen and is hence understood to be of major importance to global oceanic production and, therefore, to the role of the ocean as a sink of atmospheric CO2. At present heterotrophic denitrification and autotrophic anammox are considered the dominant sinks of fixed nitrogen. Recently, it has been suggested that the trophic nature of pelagic N2-production may have additional, "collateral" effects on the carbon cycle, where heterotrophic denitrification provides a shallow source of CO2 and autotrophic anammox a shallow sink. Here, we analyse the stoichiometries of nitrogen and associated carbon conversions in marine oxygen minimum zones (OMZ focusing on heterotrophic denitrification, autotrophic anammox, and dissimilatory nitrate reduction to nitrite and ammonium in order to test this hypothesis quantitatively. For open ocean OMZs the combined effects of these processes turn out to be clearly heterotrophic, even with high shares of the autotrophic anammox reaction in total N2-production and including various combinations of dissimilatory processes which provide the substrates to anammox. In such systems, the degree of heterotrophy (ΔCO2:ΔN2, varying between 1.7 and 6.5, is a function of the efficiency of nitrogen conversion. On the contrary, in systems like the Black Sea, where suboxic N-conversions are supported by diffusive fluxes of NH4+ originating from neighbouring waters with sulphate reduction, much lower values of ΔCO2:ΔN2 can be found. However, accounting for concomitant diffusive fluxes of CO2, the ratio approaches higher values similar to those computed for open ocean OMZs. Based on this analysis, we question the significance of collateral effects concerning the trophic

  7. Estimating the carbon budget and maximizing future carbon uptake for a temperate forest region in the U.S.

    Science.gov (United States)

    Scott D. Peckham; Stith T. Gower; Joseph Buongiorno

    2012-01-01

    Forests of the Midwest U.S. provide numerous ecosystem services. Two of these, carbon sequestration and wood production, are often portrayed as conflicting. Currently, carbon management and biofuel policies are being developed to reduce atmospheric CO2 and national dependence on foreign oil, and increase carbon storage in ecosystems. However, the biological and...

  8. Influence of ocean acidification on the complexation of iron and copper by organic ligands in estuarine waters

    NARCIS (Netherlands)

    Gledhill, M.; Achterberg, E.P.; Li, K.; Mohamed, K.N.; Rijkenberg, M.J.

    2015-01-01

    The uptake of anthropogenic atmospheric CO2 by the oceans causes a shift in the carbonate chemistry system which includes a lowering of pH; this process has been termed ocean acidification. Our understanding of the specific effects of ocean acidification on chemical speciation of trace metals, in

  9. Dissolved black carbon along the land to ocean continuum of Paraiba do Sul River, Brazil

    Science.gov (United States)

    Marques da Silva Junior, Jomar; Dittmar, Thorsten; Niggemann, Jutta; Gomes de Almeida, Marcelo; de Rezende, Carlos Eduardo

    2016-04-01

    Rivers annually carry 25-28 Tg of pyrogenic dissolved organic matter (or dissolved black carbon, DBC) into the ocean, which is equivalent to about 10% of the entire land-ocean flux of dissolved organic carbon (Jaffé et al., Science 340, 345-347). Objective of this study was to identify the main processes behind the release and turnover of DBC on a riverine catchment scale. As model system we chose the land to ocean continuum of Paraíba do Sul River (Brazil), the only river system for which long-term DBC flux data exist (Dittmar, Rezende et al., Nature Geoscience 5, 618-622). The catchment was originally covered by Atlantic rain forest (mainly C3 plants) which was almost completely destroyed over the past centuries by slash-and-burn. As a result, large amounts of wood-derived charcoal reside in the soils. Today, fire-managed pasture and sugar cane (both dominated by C4 plants) cover most of the catchment. Water samples were collected at 24 sites along the main channel of the river, at 14 sites of the main tributaries and at 21 sites along the salinity gradient in the estuary and up to 35 km offshore. Sampling was performed in the wet seasons of 2013 and 2014, and the dry season of 2013. DBC was determined on a molecular level as benzenepolycarboxylic acids after nitric acid oxidation (Dittmar, Limnology and Oceanography: Methods 6, 230-235). Stable carbon isotopes (δ13C) were determined in solid phase extractable dissolved organic carbon (SPE-DOC) to distinguish C4 and C3 sources. Our results clearly show a relationship between hydrology and DBC concentrations in the river, with highest DBC concentrations in the wet season and lowest in the dry season. This relationship indicates that DBC is mainly mobilized from the upper soil horizons during heavy rainfalls. A significant correlation between DBC concentrations and δ13C-SPE-DOC indicated that most of DBC in the river system originates from C3 plants, i.e. from the historic burning event of the Atlantic rain

  10. Liquid carbon dioxide/pulverized limestone globulsion delivery system for deep ocean storage

    Energy Technology Data Exchange (ETDEWEB)

    Swett, P.; Golomb, D.; Barry, E.; Ryan, D.; Lawton, C. [Massachusetts Univ., Lowell, MA (United States)

    2005-07-01

    Ocean storage of carbon dioxide (CO{sub 2}) raises serious environmental, technical and economic problems because a massive point injection of pure liquid CO{sub 2} at depth would create a plume of carbonic acid with a pH lower than 7. Acidified seawater is considered to be harmful to aquatic organisms. Laboratory studies have shown that injecting a globulsion consisting of CO{sub 2}, water (H{sub 2}O) and calcium carbonate (CaCO{sub 3}) instead of pure liquid CO{sub 2} results in an alkaline reaction rather than an acidic reaction. Because calcium carbonate and bicarbonate are natural ingredients of seawater, there is no expected harm due to the additive limestone. This paper presented a practical delivery system for the underwater creation of globulsion. When liquid or supercritical CO{sub 2} is mixed with a slurry of finely pulverized limestone (CaCO{sub 3}) in pure or seawater, a macro-emulsion is formed consisting of CO{sub 2} droplets coated with CaCO{sub 3} particles dispersed in water. In this study, liquid CO{sub 2} was piped to approximately 500 m depth, which is below the flash point of liquid CO{sub 2} into vapor. A slurry of pulverized limestone in seawater was also separately piped to this depth. A static mixer was mounted at the end of the pipes. Liquid CO{sub 2}, along with a slurry of pulverized limestone and ambient seawater were pumped into the mixer by a turbine. The globulsion exited from the other end of the mixer and sank like a dense plume to greater depths while entraining ambient seawater. The CaCO{sub 3}-coated globules precipitated from the neutrally buoyant plume toward the ocean bottom following equilibration. As such, the ocean was not be acidified with this method of CO{sub 2} discharging. It was concluded that even inland seas, such as the Mediterranean and Black Seas, could be considered for sequestration of a CO{sub 2}/H{sub 2}O/CaCO{sub 3} globulsion. Although adding pulverized limestone to liquid CO{sub 2} and the mixing

  11. Utility of multiple tracer distributions in calibrating models for uptake of anthropogenic CO2 by the ocean thermocline

    International Nuclear Information System (INIS)

    Peng, T.H.; Broecker, W.S.

    1985-01-01

    Two-dimensional thermocline ventilation models for the temperate North Atlantic with differing circulation patterns were calibrated to yield a tritium distribution similar to that observed during the GEOSECS survey. These models were then run for 3 He, bomb-produced 14 C, radiokrypton, and freons. They were also run for the uptake of fossil fuel CO 2 . While the models differ significantly in their ability to match the observed 3 He and 14 C distributions, these differences are not large enough to clearly single out one model as superior. This insensitivity of tracer-to-tracer ratio to model design is reflected by the near identity of the fossil fuel CO 2 uptake by the various models. This result suggests that the uptake of CO 2 by the sea is limited more by the rates of physical mixing within the sea than by gas exchange across the sea surface. If so, then the hope that models employing outcropping isopycnals will enhance the CO 2 uptake by the sea and thereby lead to a narrowing in the gap that exists for anthropogenic CO 2 budgets is not well founded. The interim strategy of using reservoir models calibrated by tracer distributions appears to be sound. 20 references, 19 figures, 5 tables

  12. Amazon River carbon dioxide outgassing fuelled by wetlands

    NARCIS (Netherlands)

    Abril, G.; Martinez, J.M.; Artigas, L.F.; Moreira-Turcq, P.; Benedetti, M.F.; Vidal, L.; Meziane, T.; Kim, J.-H.; Bernardes, M.C.; Savoye, N.; Deborde, J.; Souza, E.L.; Alberic, P.; de Souza, M.F.L.; Roland, F.

    2014-01-01

    River systems connect the terrestrial biosphere, the atmosphere and the ocean in the global carbon cycle(1). A recent estimate suggests that up to 3 petagrams of carbon per year could be emitted as carbon dioxide (CO2) from global inland waters, offsetting the carbon uptake by terrestrial

  13. Treated Wastewater Changes the Export of Dissolved Inorganic Carbon and Its Isotopic Composition and Leads to Acidification in Coastal Oceans.

    Science.gov (United States)

    Yang, Xufeng; Xue, Liang; Li, Yunxiao; Han, Ping; Liu, Xiangyu; Zhang, Longjun; Cai, Wei-Jun

    2018-04-25

    Human-induced changes in carbon fluxes across the land-ocean interface can influence the global carbon cycle, yet the impacts of rapid urbanization and establishment of wastewater treatment plants (WWTPs) on coastal ocean carbon cycles are poorly known. This is unacceptable as at present ∼64% of global municipal wastewater is treated before discharge. Here, we report surface water dissolved inorganic carbon (DIC) and sedimentary organic carbon concentrations and their isotopic compositions in the rapidly urbanized Jiaozhou Bay in northeast China as well as carbonate parameters in effluents of three large WWTPs around the bay. Using DIC, δ 13 C DIC and total alkalinity (TA) data and a tracer model, we determine the contributions to DIC from wastewater DIC input, net ecosystem production, calcium carbonate precipitation, and CO 2 outgassing. Our study shows that high-DIC and low-pH wastewater effluent represents an important source of DIC and acidification in coastal waters. In contrast to the traditional view of anthropogenic organic carbon export and degradation, we suggest that with the increase of wastewater discharge and treatment rates, wastewater DIC input may play an increasingly more important role in the coastal ocean carbon cycle.

  14. Phytoplankton Do Not Produce Carbon-Rich Organic Matter in High CO2 Oceans

    Science.gov (United States)

    Kim, Ja-Myung; Lee, Kitack; Suh, Young-Sang; Han, In-Seong

    2018-05-01

    The ocean is a substantial sink for atmospheric carbon dioxide (CO2) released as a result of human activities. Over the coming decades the dissolved inorganic C concentration in the surface ocean is predicted to increase, which is expected to have a direct influence on the efficiency of C utilization (consumption and production) by phytoplankton during photosynthesis. Here we evaluated the generality of C-rich organic matter production by examining the elemental C:N ratio of organic matter produced under conditions of varying pCO2. The data used in this analysis were obtained from a series of pelagic in situ pCO2 perturbation studies that were performed in the diverse ocean regions and involved natural phytoplankton assemblages. The C:N ratio of the resulting particulate and dissolved organic matter did not differ across the range of pCO2 conditions tested. In particular, the ratio for particulate organic C and N was found to be 6.58 ± 0.05, close to the theoretical value of 6.6.

  15. Emulating coupled atmosphere-ocean and carbon cycle models with a simpler model, MAGICC6 – Part 1: Model description and calibration

    Directory of Open Access Journals (Sweden)

    M. Meinshausen

    2011-02-01

    Full Text Available Current scientific knowledge on the future response of the climate system to human-induced perturbations is comprehensively captured by various model intercomparison efforts. In the preparation of the Fourth Assessment Report (AR4 of the Intergovernmental Panel on Climate Change (IPCC, intercomparisons were organized for atmosphere-ocean general circulation models (AOGCMs and carbon cycle models, named "CMIP3" and "C4MIP", respectively. Despite their tremendous value for the scientific community and policy makers alike, there are some difficulties in interpreting the results. For example, radiative forcings were not standardized across the various AOGCM integrations and carbon cycle runs, and, in some models, key forcings were omitted. Furthermore, the AOGCM analysis of plausible emissions pathways was restricted to only three SRES scenarios. This study attempts to address these issues. We present an updated version of MAGICC, the simple carbon cycle-climate model used in past IPCC Assessment Reports with enhanced representation of time-varying climate sensitivities, carbon cycle feedbacks, aerosol forcings and ocean heat uptake characteristics. This new version, MAGICC6, is successfully calibrated against the higher complexity AOGCMs and carbon cycle models. Parameterizations of MAGICC6 are provided. The mean of the emulations presented here using MAGICC6 deviates from the mean AOGCM responses by only 2.2% on average for the SRES scenarios. This enhanced emulation skill in comparison to previous calibrations is primarily due to: making a "like-with-like comparison" using AOGCM-specific subsets of forcings; employing a new calibration procedure; as well as the fact that the updated simple climate model can now successfully emulate some of the climate-state dependent effective climate sensitivities of AOGCMs. The diagnosed effective climate sensitivity at the time of CO2 doubling for the AOGCMs is on average 2.88 °C, about

  16. Computing the carbonate chemistry of the coral calcifying medium and its response to ocean acidification.

    Science.gov (United States)

    Raybaud, Virginie; Tambutté, Sylvie; Ferrier-Pagès, Christine; Reynaud, Stéphanie; Venn, Alexander A; Tambutté, Éric; Nival, Paul; Allemand, Denis

    2017-07-07

    Critical to determining vulnerability or resilience of reef corals to Ocean Acidification (OA) is a clearer understanding of the extent to which corals can control carbonate chemistry in their Extracellular Calcifying Medium (ECM) where the CaCO 3 skeleton is produced. Here, we employ a mathematical framework to calculate ECM aragonite saturation state (Ω arag.(ECM) ) and carbonate system ion concentration using measurements of calcification rate, seawater characteristics (temperature, salinity and pH) and ECM pH (pH (ECM) ). Our calculations of ECM carbonate chemistry at current-day seawater pH, indicate that Ω arag.(ECM) ranges from ∼10 to 38 (mean 20.41), i.e. about 5 to 6-fold higher than seawater. Accordingly, Dissolved Inorganic Carbon (DIC) and Total Alkalinity (TA) were calculated to be around 3 times higher in the ECM than in seawater. We also assessed the effects of acidification on ECM chemical properties of the coral Stylophora pistillata. At reduced seawater pH our calculations indicate that Ω arag.(ECM) remains almost constant. DIC (ECM) and TA (ECM) gradually increase as seawater pH declines, reaching values about 5 to 6-fold higher than in seawater, respectively for DIC and TA. We propose that these ECM characteristics buffer the effect of acidification and explain why certain corals continue to produce CaCO 3 even when seawater chemistry is less favourable. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Coupling of oceanic carbon and nitrogen: A window to spatially resolved quantitative reconstruction of nitrate inventories

    Science.gov (United States)

    Glock, N.; Liebetrau, V.; Gorb, S.; Wallmann, K. J. G.; Erdem, Z.; Schönfeld, J.; Eisenhauer, A.

    2017-12-01

    Anthropogenic impact has led to a severe acceleration of the global nitrogen cycle. Every second nitrogen atom in the biosphere may now originate from anthropogenic sources such as chemical fertilizers and the burning of fossil fuels. A quantitative reconstruction of past reactive nitrogen inventories is invaluable to facilitate projections for future scenarios and calibrations for such paleoproxies should be done as long the natural signature is still visible. Here we present a first quantitative reconstruction of nitrate concentrations in intermediate water depths of the Peruvian oxygen minimum zone over the last deglaciation using the pore density in the benthic foraminiferal species Bolivina spissa. A comparison of the nitrate reconstruction to the stable carbon isotope (δ13C) record reveals a strong coupling between the carbon and nitrogen cycles. The linear correlation between δ13C and nitrate availability remained stable over the last 22,000 years, facilitating the use of δ13C records as a quantitative nitrate proxy. The combination of the pore density record with δ13C records shows an elevated oceanic nitrate inventory during the Last Glacial Maximum as compared to the Holocene. Our novel proxy approach is consistent with the results of previous δ15N-based biogeochemical modeling studies, and thus provides sound estimates of the nitrate inventory in the glacial and deglacial ocean.

  18. An Ocean Basin of Dirt? Using Molecular Biomarkers and Radiocarbon to Identify Organic Carbon Sources and their Preservation in the Arctic Ocean

    Science.gov (United States)

    Harvey, H.; Belicka, L. L.

    2005-12-01

    In the modern Arctic Ocean, primary production in waters over the broad continental shelves and under ice contributes an estimated 250 Mt/yr of POC to Arctic waters. The delivery of terrestrial material from large rivers, ice transport and through coastal erosion adds at least an additional 12 Mt/yr of POC. Although the marine organic carbon signal in Arctic Ocean exceeds that of terrestrial carbon by an order or magnitude or more, recent evidence suggests that this balance is not maintained and significant fractions of terrestrial carbon is preserved in sediments. Using an integrated approach combining lipid biomarkers and radiocarbon dating in particles and sediments, the process of organic carbon recycling and historical changes in its sources and preservation has been examined. A suite of lipid biomarkers in particles and sediments of western Arctic shelves and basins were measured and principle components analysis (PCA) used to allow a robust comparison among the 120+ individual compounds to assign organic sources and relative inputs. Offshore particles from the chlorophyll maximum contained abundant algal markers (e.g. 20:5 and 22:6 FAMEs), low concentrations of terrestrial markers (amyrins and 24-ethylcholest-5-en-3b-ol), and reflected modern 14C values. Particles present in deeper halocline waters also reflect marine production, but a portion of older, terrestrial carbon accompanies the sinking of the spring bloom. Surface and deeper sediments of basins contain older organic carbon and low concentrations of algal biomarkers, suggesting that marine carbon produced in surface waters is rapidly recycled. Taken together, these observations suggest that marine derived organic matter produced in shallow waters fuels carbon cycling, but relatively small amounts are preserved in sediments. As a result, the organic carbon preserved in sediments contrasts sharply to that typically observed in lower latitudes, with an increasing terrestrial signature with distance

  19. Effects of ocean acidification and hydrodynamic conditions on carbon metabolism and dissolved organic carbon (DOC) fluxes in seagrass populations.

    Science.gov (United States)

    Egea, Luis G; Jiménez-Ramos, Rocío; Hernández, Ignacio; Bouma, Tjeerd J; Brun, Fernando G

    2018-01-01

    Global change has been acknowledged as one of the main threats to the biosphere and its provision of ecosystem services, especially in marine ecosystems. Seagrasses play a critical ecological role in coastal ecosystems, but their responses to ocean acidification (OA) and climate change are not well understood. There have been previous studies focused on the effects of OA, but the outcome of interactions with co-factors predicted to alter during climate change still needs to be addressed. For example, the impact of higher CO2 and different hydrodynamic regimes on seagrass performance remains unknown. We studied the effects of OA under different current velocities on productivity of the seagrass Zostera noltei, using changes in dissolved oxygen as a proxy for the seagrass carbon metabolism, and release of dissolved organic carbon (DOC) in a four-week experiment using an open-water outdoor mesocosm. Under current pH conditions, increasing current velocity had a positive effect on productivity, but this depended on shoot density. However, this positive effect of current velocity disappeared under OA conditions. OA conditions led to a significant increase in gross production rate and respiration, suggesting that Z. noltei is carbon-limited under the current inorganic carbon concentration of seawater. In addition, an increase in non-structural carbohydrates was found, which may lead to better growing conditions and higher resilience in seagrasses subjected to environmental stress. Regarding DOC flux, a direct and positive relationship was found between current velocity and DOC release, both under current pH and OA conditions. We conclude that OA and high current velocity may lead to favourable growth scenarios for Z. noltei populations, increasing their productivity, non-structural carbohydrate concentrations and DOC release. Our results add new dimensions to predictions on how seagrass ecosystems will respond to climate change, with important implications for the

  20. Effects of ocean acidification and hydrodynamic conditions on carbon metabolism and dissolved organic carbon (DOC fluxes in seagrass populations.

    Directory of Open Access Journals (Sweden)

    Luis G Egea

    Full Text Available Global change has been acknowledged as one of the main threats to the biosphere and its provision of ecosystem services, especially in marine ecosystems. Seagrasses play a critical ecological role in coastal ecosystems, but their responses to ocean acidification (OA and climate change are not well understood. There have been previous studies focused on the effects of OA, but the outcome of interactions with co-factors predicted to alter during climate change still needs to be addressed. For example, the impact of higher CO2 and different hydrodynamic regimes on seagrass performance remains unknown. We studied the effects of OA under different current velocities on productivity of the seagrass Zostera noltei, using changes in dissolved oxygen as a proxy for the seagrass carbon metabolism, and release of dissolved organic carbon (DOC in a four-week experiment using an open-water outdoor mesocosm. Under current pH conditions, increasing current velocity had a positive effect on productivity, but this depended on shoot density. However, this positive effect of current velocity disappeared under OA conditions. OA conditions led to a significant increase in gross production rate and respiration, suggesting that Z. noltei is carbon-limited under the current inorganic carbon concentration of seawater. In addition, an increase in non-structural carbohydrates was found, which may lead to better growing conditions and higher resilience in seagrasses subjected to environmental stress. Regarding DOC flux, a direct and positive relationship was found between current velocity and DOC release, both under current pH and OA conditions. We conclude that OA and high current velocity may lead to favourable growth scenarios for Z. noltei populations, increasing their productivity, non-structural carbohydrate concentrations and DOC release. Our results add new dimensions to predictions on how seagrass ecosystems will respond to climate change, with important

  1. Monthly dynamics of carbon dioxide exchange across the sea surface of the Arctic Ocean in response to changes in gas transfer velocity and partial pressure of CO2 in 2010

    Directory of Open Access Journals (Sweden)

    Iwona Wrobel

    2017-10-01

    Full Text Available The Arctic Ocean (AO is an important basin for global oceanic carbon dioxide (CO2 uptake, but the mechanisms controlling air–sea gas fluxes are not fully understood, especially over short and long timescales. The oceanic sink of CO2 is an important part of the global carbon budget. Previous studies have shown that in the AO differences in the partial pressure of CO2 (ΔpCO2 and gas transfer velocity (k both contribute significantly to interannual air–sea CO2 flux variability, but that k is unimportant for multidecadal variability. This study combined Earth Observation (EO data collected in 2010 with the in situ pCO2 dataset from Takahashi et al. (2009 (T09 using a recently developed software toolbox called FluxEngine to determine the importance of k and ΔpCO2 on CO2 budgets in two regions of the AO – the Greenland Sea (GS and the Barents Sea (BS with their continental margins. Results from the study indicate that the variability in wind speed and, hence, the gas transfer velocity, generally play a major role in determining the temporal variability of CO2 uptake, while variability in monthly ΔpCO2 plays a major role spatially, with some exceptions.

  2. Carbon Burial at the Land Ocean Interface: Climate vs Human Drivers

    Science.gov (United States)

    Bianchi, T. S.; Smeaton, C.; Cui, X.; Howe, J. A.; Austin, W.

    2017-12-01

    Fjords are connectors between the terrestrial and marine systems and are known as globally significant hotspots for the burial (Smith et al., 2014) and long-term storage (Smeaton et al., 2016) of carbon (C). The glacial geomorphology of fjords and their catchment results in the terrestrial and marine environments being strongly coupled more so than other estuary types. The clearest example of this is the terrestrial C subsidy to these sediment, it is estimated that globally 55-62% of C held in fjord sediments are terrestrially derived (Cui et al., 2016). Yet it is largely unknown how climatic and human forcing drives the transfer of terrestrial C to marine sediments. Here we, examine the role of late Holocene climate and human activity on the transfer of C from the terrestrial to marine environment along the North Atlantic Margin. Loch Sunart a Scottish fjord sits at the land ocean interface of the North Atlantic. The catchment of the fjord has been shown to be sensitive to local and regional climatic change (Gillibrand et al., 2005) and the fjord sediments have been able to record these changes in Climate (Cage and Austin, 2010). Using a long (22 m) sedimentary record we discuss our understanding of mid to late Holocene regional climate and its impact on terrestrial C transfer to the coastal ocean. Alongside this we examine the role of humans on the landscape and their impact on the transfer of terrestrial C on the coastal ocean. The results from this study will further our understanding of the long-term drivers of terrestrial C transfer to the coastal ocean. Potentially this research provides insights on future C transfers under a changing future climate allowing the importance of fjords as a climate regulation service to be reassessed.

  3. Dissolved Inorganic Carbon, Alkalinity, pH, temperature, salinity, and other variables collected from profile observations using CTD, discrete bottles, and other instruments from February 12, 1985 to June 17, 2009, as synthesized in the Pacific Ocean Interior Carbon (PACIFICA) Database (NODC Accession 0110865)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — PACIFICA Data Synthesis Project PACIFICA (PACIFic ocean Interior CArbon) was an international collaborative project for the data synthesis of ocean interior carbon...

  4. Spiraling pathways of global deep waters to the surface of the Southern Ocean

    OpenAIRE

    Tamsitt, Veronica; Drake, Henri F.; Morrison, Adele K.; Talley, Lynne D.; Dufour, Carolina O.; Gray, Alison R.; Griffies, Stephen M.; Mazloff, Matthew R.; Sarmiento, Jorge L.; Wang, Jinbo; Weijer, Wilbert

    2017-01-01

    Upwelling of global deep waters to the sea surface in the Southern Ocean closes the global overturning circulation and is fundamentally important for oceanic uptake of carbon and heat, nutrient resupply for sustaining oceanic biological production, and the melt rate of ice shelves. However, the exact pathways and role of topography in Southern Ocean upwelling remain largely unknown. Here we show detailed upwelling pathways in three dimensions, using hydrographic observations and particle trac...

  5. An experimental set-up to study carbon, water, and nitrate uptake rates by hydroponically grown plants.

    Science.gov (United States)

    Andriolo, J L; Le Bot, J; Gary, C; Sappe, G; Orlando, P; Brunel, B; Sarrouy, C

    1996-01-01

    The experimental system described allows concomitant hourly measurements of CO2, H2O, and NO3 uptake rates by plants grown hydroponically in a greenhouse. Plants are enclosed in an airtight chamber through which air flows at a controlled speed. Carbon dioxide exchange and transpiration rates are determined from respective differences of concentrations of CO2 and water vapor of the air at the system inlet and outlet. This set-up is based on the "open-system" principle with improvements made on existing systems. For instance, propeller anemometers are used to monitor air flow rates in the chamber. From their signal it is possible to continuously adjust air speed to changing environmental conditions and plant activity. The air temperature inside the system therefore never rises above that outside. Water and NO3 uptake rates are calculated at time intervals from changes in the volume and the NO3 concentration of the nutrient solution in contact with the roots. The precise measurement of the volume of solution is achieved using a balance which has a higher precision than any liquid level sensors. Nitrate concentration is determined in the laboratory from aliquots of solution sampled at time intervals. A number of test runs are reported which validate the measurements and confirm undisturbed conditions within the system. Results of typical diurnal changes in CO2, H2O, and NO3 uptake rates by fruiting tomato plants are also presented.

  6. Oceanic acidification affects marine carbon pump and triggers extended marine oxygen holes.

    Science.gov (United States)

    Hofmann, Matthias; Schellnhuber, Hans-Joachim

    2009-03-03

    Rising atmospheric CO(2) levels will not only drive future global mean temperatures toward values unprecedented during the whole Quaternary but will also lead to massive acidification of sea water. This constitutes by itself an anthropogenic planetary-scale perturbation that could significantly modify oceanic biogeochemical fluxes and severely damage marine biota. As a step toward the quantification of such potential impacts, we present here a simulation-model-based assessment of the respective consequences of a business-as-usual fossil-fuel-burning scenario where a total of 4,075 Petagrams of carbon is released into the atmosphere during the current millennium. In our scenario, the atmospheric pCO(2) level peaks at approximately 1,750 microatm in the year 2200 while the sea-surface pH value drops by >0.7 units on global average, inhibiting the growth of marine calcifying organisms. The study focuses on quantifying 3 major concomitant effects. The first one is a significant (climate-stabilizing) negative feedback on rising pCO(2) levels as caused by the attenuation of biogenic calcification. The second one is related to the biological carbon pump. Because mineral ballast, notably CaCO(3), is found to play a dominant role in carrying organic matter through the water column, a reduction of its export fluxes weakens the strength of the biological carbon pump. There is, however, a third effect with severe consequences: Because organic matter is oxidized in shallow waters when mineral-ballast fluxes weaken, oxygen holes (hypoxic zones) start to expand considerably in the oceans in our model world--with potentially harmful impacts on a variety of marine ecosystems.

  7. Increasing coastal slump activity impacts the release of sediment and organic carbon into the Arctic Ocean

    Directory of Open Access Journals (Sweden)

    J. L. Ramage

    2018-03-01

    Full Text Available Retrogressive thaw slumps (RTSs are among the most active thermokarst landforms in the Arctic and deliver a large amount of material to the Arctic Ocean. However, their contribution to the organic carbon (OC budget is unknown. We provide the first estimate of the contribution of RTSs to the nearshore OC budget of the Yukon Coast, Canada, and describe the evolution of coastal RTSs between 1952 and 2011 in this area. We (1 describe the evolution of RTSs between 1952 and 2011; (2 calculate the volume of eroded material and stocks of OC mobilized through slumping, including soil organic carbon (SOC and dissolved organic carbon (DOC; and (3 estimate the OC fluxes mobilized through slumping between 1972 and 2011. We identified RTSs using high-resolution satellite imagery from 2011 and geocoded aerial photographs from 1952 and 1972. To estimate the volume of eroded material, we applied spline interpolation on an airborne lidar dataset acquired in July 2013. We inferred the stocks of mobilized SOC and DOC from existing related literature. Our results show a 73 % increase in the number of RTSs and 14 % areal expansion between 1952 and 2011. In the study area, RTSs displaced at least 16.6×106 m3 of material, 53 % of which was ice, and mobilized 145.9×106 kg of OC. Between 1972 and 2011, 49 RTSs displaced 8.6×103 m3 yr−1 of material, adding 0.6 % to the OC flux released by coastal retreat along the Yukon Coast. Our results show that the contribution of RTSs to the nearshore OC budget is non-negligible and should be included when estimating the quantity of OC released from the Arctic coast to the ocean.

  8. The Evolution of Deep Ocean Chemistry and Respired Carbon in the Eastern Equatorial Pacific Over the Last Deglaciation

    Science.gov (United States)

    de la Fuente, Maria; Calvo, Eva; Skinner, Luke; Pelejero, Carles; Evans, David; Müller, Wolfgang; Povea, Patricia; Cacho, Isabel

    2017-12-01

    It has been shown that the deep Eastern Equatorial Pacific (EEP) region was poorly ventilated during the Last Glacial Maximum (LGM) relative to Holocene values. This finding suggests a more efficient biological pump, which indirectly supports the idea of increased carbon storage in the deep ocean contributing to lower atmospheric CO2 during the last glacial. However, proxies related to respired carbon are needed in order to directly test this proposition. Here we present Cibicides wuellerstorfi B/Ca ratios from Ocean Drilling Program Site 1240 measured by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) as a proxy for deep water carbonate saturation state (Δ[CO32-], and therefore [CO32-]), along with δ13C measurements. In addition, the U/Ca ratio in foraminiferal coatings has been analyzed as an indicator of oxygenation changes. Our results show lower [CO32-], δ13C, and [O2] values during the LGM, which would be consistent with higher respired carbon levels in the deep EEP driven, at least in part, by reduced deep water ventilation. However, the difference between LGM and Holocene [CO32-] observed at our site is relatively small, in accordance with other records from across the Pacific, suggesting that a "counteracting" mechanism, such as seafloor carbonate dissolution, also played a role. If so, this mechanism would have increased average ocean alkalinity, allowing even more atmospheric CO2 to be "sequestered" by the ocean. Therefore, the deep Pacific Ocean very likely stored a significant amount of atmospheric CO2 during the LGM, specifically due to a more efficient biological carbon pump and also an increase in average ocean alkalinity.

  9. Summertime calcium carbonate undersaturation in shelf waters of the western Arctic Ocean – how biological processes exacerbate the impact of ocean acidification

    Directory of Open Access Journals (Sweden)

    N. R. Bates

    2013-08-01

    Full Text Available The Arctic Ocean accounts for only 4% of the global ocean area, but it contributes significantly to the global carbon cycle. Recent observations of seawater CO2-carbonate chemistry in shelf waters of the western Arctic Ocean, primarily in the Chukchi Sea, from 2009 to 2011 indicate that bottom waters are seasonally undersaturated with respect to calcium carbonate (CaCO3 minerals, particularly aragonite. Nearly 40% of sampled bottom waters on the shelf have saturation states less than one for aragonite (i.e., Ωaragonite 3-secreting organisms, while 80% of bottom waters present had Ωaragonite values less than 1.5. Our observations indicate seasonal reduction of saturation states (Ω for calcite (Ωcalcite and aragonite (Ωaragonite in the subsurface in the western Arctic by as much as 0.8 and 0.5, respectively. Such data indicate that bottom waters of the western Arctic shelves were already potentially corrosive for biogenic and sedimentary CaCO3 for several months each year. Seasonal changes in Ω are imparted by a variety of factors such as phytoplankton photosynthesis, respiration/remineralization of organic matter and air–sea gas exchange of CO2. Combined, these processes either increase or enhance in surface and subsurface waters, respectively. These seasonal physical and biological processes also act to mitigate or enhance the impact of Anthropocene ocean acidification (OA on Ω in surface and subsurface waters, respectively. Future monitoring of the western Arctic shelves is warranted to assess the present and future impact of ocean acidification and seasonal physico-biogeochemical processes on Ω values and Arctic marine ecosystems.

  10. Needle age and season influence photosynthetic temperature response and total annual carbon uptake in mature Picea mariana trees

    Science.gov (United States)

    Jensen, Anna M.; Warren, Jeffrey M.; Hanson, Paul J.; Childs, Joanne; Wullschleger, Stan D.

    2015-01-01

    Background and Aims The carbon (C) balance of boreal terrestrial ecosystems is sensitive to increasing temperature, but the direction and thresholds of responses are uncertain. Annual C uptake in Picea and other evergreen boreal conifers is dependent on seasonal- and cohort-specific photosynthetic and respiratory temperature response functions, so this study examined the physiological significance of maintaining multiple foliar cohorts for Picea mariana trees within an ombrotrophic bog ecosystem in Minnesota, USA. Methods Measurements were taken on multiple cohorts of needles for photosynthetic capacity, foliar respiration (Rd) and leaf biochemistry and morphology of mature trees from April to October over 4 years. The results were applied to a simple model of canopy photosynthesis in order to simulate annual C uptake by cohort age under ambient and elevated temperature scenarios. Key Results Temperature responses of key photosynthetic parameters [i.e. light-saturated rate of CO2 assimilation (Asat), rate of Rubisco carboxylation (Vcmax) and electron transport rate (Jmax)] were dependent on season and generally less responsive in the developing current-year (Y0) needles compared with 1-year-old (Y1) or 2-year-old (Y2) foliage. Temperature optimums ranged from 18·7 to 23·7, 31·3 to 38·3 and 28·7 to 36·7 °C for Asat, Vcmax and Jmax, respectively. Foliar cohorts differed in their morphology and photosynthetic capacity, which resulted in 64 % of modelled annual stand C uptake from Y1&2 cohorts (LAI 0·67 m2 m−2) and just 36 % from Y0 cohorts (LAI 0·52 m2 m−2). Under warmer climate change scenarios, the contribution of Y0 cohorts was even less; e.g. 31 % of annual C uptake for a modelled 9 °C rise in mean summer temperatures. Results suggest that net annual C uptake by P. mariana could increase under elevated temperature, and become more dependent on older foliar cohorts. Conclusions Collectively, this study illustrates the physiological and

  11. Stable carbon and oxygen isotope signatures in molluscan shells under ocean acidification

    Science.gov (United States)

    Nishida, K.; Hayashi, M.; Suzuki, A.; Sato, M.; Nojiri, Y.

    2017-12-01

    Stable carbon and oxygen isotope compositions (δ13C, δ18O) of biogenic carbonate have been widely used for many paleoclimate, paleoecological, and biomineralization studies. δ13C of molluscan shells reflects the mixing of δ13C of dissolved inorganic carbon (DIC) of seawater and respiratory carbon. Previous studies reported physiological effects on molluscs by ocean acidification, and thus the metabolic changes could potentially appear in shell δ13C as changes in a fraction of two carbon sources. In addition, shell δ18O, a commonly used proxy of seawater temperature and seawater δ18O, is also affected by seawater carbonate chemistry. As changes in the marine carbonate system, such as pH and pCO2, have occurred in the past 300 million years, to estimate pH effect on paleotemperature reconstruction is important. Here, we experimentally examined acidification effects on shell δ13C and δ18O of two species of clams for understanding of environmental and physiological proxies. Juvenile specimens of bloody clam Scapharca broughtonii and Japanese surf clam Pseudocardium sachalinense were cultured at five (400, 600, 800, 1000, and 1200 µatm, P. sachalinense) or six (280, 400, 600, 800, 1000, and 1200 µatm, S. broughtonii) different pCO2 levels using CO2 control system of the Demonstration Laboratory, MERI, Japan. Significant negative correlations between shell δ13C and pH appeared in S. broughtonii, which showed non-significant pH effects on calcification, and the slope of the relationship of shell carbonate was lower than that of seawater DIC. On the other hand, in P. sachalinense which showed a decrease in calcification at low-pH treatment, the slopes of the relationship between shell δ13C and pH was roughly the same as that of seawater DIC. Thus, the extrapallial fluid of P. sachalinense might more strongly affected by acidified seawater than S. broughtonii. The results of two species might be attributable to differences in physiological responses to

  12. The dynamics of CO2 fixation in the Southern Ocean as indicated by carboxylase activities and organic carbon isotopic ratios

    International Nuclear Information System (INIS)

    Fontugne, M.

    1991-01-01

    Recent studies have suggested a direct relationship between the dissolved CO 2 concentration and carbon isotopic composition of phytoplankton in surface ocean. Thus, measurement of δ 13 C of planktonic organic matter in deep-sea ocean cores can potentially yield a record of the past atmospheric CO 2 variations. However, results are presented from 3 cruises in Indian and Atlantic sectors of the Southern Ocean (between 40-66degS) in which biochemical and physiological factors associated with photosynthetic processes lead to carbon isotopic fractionation by phytoplankton which cannot be directly related to variations within the mineral carbon pool. Simultaneous measurements of the carboxylase activities in the 13 C/ 12 C ratio of particulate organic carbon show that there is a large variability in phytoplankton carbon metabolism, especially on a seasonal scale, in spite of a relative uniformity of the environmental conditions. Phytoplankton carbon metabolism is clearly a main factor governing variations in the stable isotopic composition of organic matter in the euphotic layer. Interrelationships between light, Rubiso activity and δ 13 C are clearly shown by the data. Heterotrophic processes may also influence the carbon isotope mass balance, especially during the break-up of the ice pack. In addition to the influence of photosynthetic metabolism, the effect of the meridoneal temperature gradient is also verified by the data set. (author). 24 refs.; 5 figs

  13. Sinking rates and ballast composition of particles in the Atlantic Ocean: implications for the organic carbon fluxes to the deep ocean

    Science.gov (United States)

    Fischer, G.; Karakaş, G.

    2009-01-01

    The flux of materials to the deep sea is dominated by larger, organic-rich particles with sinking rates varying between a few meters and several hundred meters per day. Mineral ballast may regulate the transfer of organic matter and other components by determining the sinking rates, e.g. via particle density. We calculated particle sinking rates from mass flux patterns and alkenone measurements applying the results of sediment trap experiments from the Atlantic Ocean. We have indication for higher particle sinking rates in carbonate-dominated production systems when considering both regional and seasonal data. During a summer coccolithophorid bloom in the Cape Blanc coastal upwelling off Mauritania, particle sinking rates reached almost 570 m per day, most probably due the fast sedimentation of densely packed zooplankton fecal pellets, which transport high amounts of organic carbon associated with coccoliths to the deep ocean despite rather low production. During the recurring winter-spring blooms off NW Africa and in opal-rich production systems of the Southern Ocean, sinking rates of larger particles, most probably diatom aggregates, showed a tendency to lower values. However, there is no straightforward relationship between carbonate content and particle sinking rates. This could be due to the unknown composition of carbonate and/or the influence of particle size and shape on sinking rates. It also remains noticeable that the highest sinking rates occurred in dust-rich ocean regions off NW Africa, but this issue deserves further detailed field and laboratory investigations. We obtained increasing sinking rates with depth. By using a seven-compartment biogeochemical model, it was shown that the deep ocean organic carbon flux at a mesotrophic sediment trap site off Cape Blanc can be captured fairly well using seasonal variable particle sinking rates. Our model provides a total organic carbon flux of 0.29 Tg per year down to 3000 m off the NW African upwelling

  14. Straightforward synthesis of a triazine-based porous carbon with high gas-uptake capacities

    DEFF Research Database (Denmark)

    Hu, Xinming; Chen, Qi; Zhao, Yan Chao

    2014-01-01

    A triazine-based porous carbon material (TPC-1) was prepared directly from a fluorinated aromatic nitrile in molten zinc chloride. Trimerization of the nitrile and subsequent defluorination carbonization of the polymeric network result in the formation of TPC-1. The defluorination process is reve...

  15. Toward Reducing Uncertainties in Biospheric Carbon Uptake in the American West: An Atmospheric Perspective

    Science.gov (United States)

    Lin, J. C.; Stephens, B. B.; Mallia, D.; Wu, D.; Jacobson, A. R.

    2015-12-01

    Despite the need for an understanding of terrestrial biospheric carbon fluxes to account for carbon cycle feedbacks and predict future CO2 concentrations, knowledge of such fluxes at the regional scale remains poor. This is particularly true in mountainous areas, where lack of observations combined with difficulties in their interpretation lead to significant uncertainties. Yet mountainous regions are also where significant forest cover and biomass are found—areas that have the potential to serve as carbon sinks. In particular, understanding carbon fluxes in the American West is of critical importance for the U.S. carbon budget, as the large area and biomass indicate potential for carbon sequestration. However, disturbances such as drought, insect outbreak, and wildfires in this region can introduce significant perturbations to the carbon cycle and thereby affect the amount of carbon sequestered by vegetation in the Rockies. To date, there have been few atmospheric CO2 observations in the American Rockies due to a combination of difficulties associated with logistics and interpretation of the measurements in the midst of complex terrain. Among the few sites are those associated with NCAR's Regional Atmospheric Continuous CO2 Network in the Rocky Mountains (Rocky RACCOON). As CO2 observations in mountainous areas increase in the future, it is imperative that they can be properly interpreted to yield information about biospheric carbon fluxes. In this paper, we will present CO2 observations from RACCOON, along with atmospheric simulations that attempt to extract information about biospheric carbon fluxes in the Western U.S. from these observations. We show that atmospheric models can significantly misinterpret the CO2 observations, leading to large errors in the retrieved biospheric fluxes, due to erroneous atmospheric flows. Recommendations for ways to minimize such errors and properly link the CO2 concentrations to biospheric fluxes are discussed.

  16. Edge effects resulting from forest fragmentation enhance carbon uptake and its vulnerability to climate change in temperate broadleaf forests

    Science.gov (United States)

    Reinmann, A.; Hutyra, L.

    2016-12-01

    Forest fragmentation resulting from land use and land cover change is a ubiquitous, ongoing global phenomenon with profound impacts on the growing conditions of the world's remaining forest. However, our understanding of forest carbon dynamics and their response to climate largely comes from unfragmented forest systems, which presents an important mismatch between the landscapes we study and those we aim to characterize. The temperate broadleaf forest makes a large contribution to the global terrestrial carbon sink, but is also the most heavily fragmented forest biome in the world. We use field measurements and geospatial analyses to characterize carbon dynamics in temperate broadleaf forest fragments. We show that forest growth and biomass increase by 89 ± 17% and 64 ± 12%, respectively, from the forest interior to edge. These ecosystem edge enhancements are not currently captured by models or approaches to quantifying regional C balance, but across southern New England, USA it increases carbon uptake and storage by 12.5 ± 2.9% and 9.6 ± 1.4%, respectively. However, we also find that forest growth near the edge declines three times faster than in the interior in response to heat stress during the growing season. Using climate projections, we show that future heat stress could reduce the forest edge growth enhancement by one-third by the end of the century. These findings contrast studies of edge effects in the world's other major forest biomes and indicate that the strength of the temperate broadleaf forest carbon sink and its capacity to mitigate anthropogenic carbon emissions may be stronger, but also more sensitive to climate change than previous estimates suggest.

  17. Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution

    Science.gov (United States)

    Rau, Gregory Hudson

    2014-07-01

    A system for forming metal hydroxide from a metal carbonate utilizes a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide.

  18. Arctic Ocean CO2 uptake: an improved multiyear estimate of the air-sea CO2 flux incorporating chlorophyll a concentrations

    Science.gov (United States)

    Yasunaka, Sayaka; Siswanto, Eko; Olsen, Are; Hoppema, Mario; Watanabe, Eiji; Fransson, Agneta; Chierici, Melissa; Murata, Akihiko; Lauvset, Siv K.; Wanninkhof, Rik; Takahashi, Taro; Kosugi, Naohiro; Omar, Abdirahman M.; van Heuven, Steven; Mathis, Jeremy T.

    2018-03-01

    We estimated monthly air-sea CO2 fluxes in the Arctic Ocean and its adjacent seas north of 60° N from 1997 to 2014. This was done by mapping partial pressure of CO2 in the surface water (pCO2w) using a self-organizing map (SOM) technique incorporating chlorophyll a concentration (Chl a), sea surface temperature, sea surface salinity, sea ice concentration, atmospheric CO2 mixing ratio, and geographical position. We applied new algorithms for extracting Chl a from satellite remote sensing reflectance with close examination of uncertainty of the obtained Chl a values. The overall relationship between pCO2w and Chl a was negative, whereas the relationship varied among seasons and regions. The addition of Chl a as a parameter in the SOM process enabled us to improve the estimate of pCO2w, particularly via better representation of its decline in spring, which resulted from biologically mediated pCO2w reduction. As a result of the inclusion of Chl a, the uncertainty in the CO2 flux estimate was reduced, with a net annual Arctic Ocean CO2 uptake of 180 ± 130 Tg C yr-1. Seasonal to interannual variation in the CO2 influx was also calculated.

  19. Invariance of the carbonate chemistry of the South China Sea from the glacial period to the Holocene and its implications to the Pacific Ocean carbonate system

    Science.gov (United States)

    Luo, Yiming; Kienast, Markus; Boudreau, Bernard P.

    2018-06-01

    Substantial and correlated changes in marine carbonate (CaCO3) content of oceanic sediments commonly accompany the transitions from cold glacial periods to warm interglacial periods. The South China Sea (SCS) is said to be ocean-dominated at depth, and its CaCO3 records should reflect and preserve the effects of changes in the carbonate chemistry of the (western) Pacific Ocean. Using published and newly acquired CaCO3 data and a model for carbonate compensation dynamics, we show that a significant change with respect to carbonate saturation is unlikely to have occurred in the SCS during the last glacial-interglacial transition. Instead, the results from a carbonate deposition model argue that the saturation state of the SCS was largely invariant; a separate diagenetic model argues that changes in sediment CaCO3 content can be explained by alterations in lithogenic input. In turn, this could indicate that the carbonate ion concentration of the (western) Pacific at depths shallower than the sill to the SCS (ca. 2,400 m) has not changed appreciably between the last glacial period and the present interglacial.

  20. Accelerated Carbonation of Steel Slags Using CO{sub 2} Diluted Sources: CO{sub 2} Uptakes and Energy Requirements

    Energy Technology Data Exchange (ETDEWEB)

    Baciocchi, Renato, E-mail: baciocchi@ing.uniroma2.it; Costa, Giulia [Department of Civil Engineering and Computer Science Engineering, University of Rome “Tor Vergata”, Rome (Italy); Polettini, Alessandra; Pomi, Raffaella; Stramazzo, Alessio [Department of Civil and Environmental Engineering, University of Rome “La Sapienza”, Rome (Italy); Zingaretti, Daniela [Department of Civil Engineering and Computer Science Engineering, University of Rome “Tor Vergata”, Rome (Italy)

    2016-01-18

    This work presents the results of carbonation experiments performed on Basic Oxygen Furnace (BOF) steel slag samples employing gas mixtures containing 40 and 10% CO{sub 2} vol. simulating the gaseous effluents of gasification and combustion processes respectively, as well as 100% CO{sub 2} for comparison purposes. Two routes were tested, the slurry-phase (L/S = 5 l/kg, T = 100°C and Ptot = 10 bar) and the thin-film (L/S = 0.3–0.4 l kg, T = 50°C and Ptot = 7–10 bar) routes. For each one, the CO{sub 2} uptake achieved as a function of the reaction time was analyzed and on this basis, the energy requirements associated with each carbonation route and gas mixture composition were estimated considering to store the CO{sub 2} emissions of a medium size natural gas fired power plant (20 MW). For the slurry-phase route, maximum CO{sub 2} uptakes ranged from around 8% at 10% CO{sub 2}, to 21.1% (BOF-a) and 29.2% (BOF-b) at 40% CO{sub 2} and 32.5% (BOF-a) and 40.3% (BOF-b) at 100% CO{sub 2}. For the thin-film route, maximum uptakes of 13% (BOF-c) and 19.5% (BOF-d) at 40% CO{sub 2}, and 17.8% (BOF-c) and 20.2% (BOF-d) at 100% were attained. The energy requirements of the two analyzed process routes appeared to depend chiefly on the CO{sub 2} uptake of the slag. For both process route, the minimum overall energy requirements were found for the tests with 40% CO{sub 2} flows (i.e., 1400−1600 MJ/t{sub CO{sub 2}} for the slurry-phase and 2220 – 2550 MJ/t{sub CO{sub 2}} for the thin-film route).

  1. Radiocarbon Content of Dissolved Organic Carbon in the South Indian Ocean

    Science.gov (United States)

    Bercovici, S. K.; McNichol, A. P.; Xu, L.; Hansell, D. A.

    2018-01-01

    We report four profiles of the radiocarbon content of dissolved organic carbon (DOC) spanning the South Indian Ocean (SIO), ranging from the Polar Front (56°S) to the subtropics (29°S). Surface waters held mean DOC Δ14C values of -426 ± 6‰ ( 4,400 14C years) at the Polar Front and DOC Δ14C values of -252 ± 22‰ ( 2,000 14C years) in the subtropics. At depth, Circumpolar Deep Waters held DOC Δ14C values of -491 ± 13‰ ( 5,400 years), while values in Indian Deep Water were more depleted, holding DOC Δ14C values of -503 ± 8‰ ( 5,600 14C years). High-salinity North Atlantic Deep Water intruding into the deep SIO had a distinctly less depleted DOC Δ14C value of -481 ± 8‰ ( 5,100 14C years). We use multiple linear regression to assess the dynamics of DOC Δ14C values in the deep Indian Ocean, finding that their distribution is characteristic of water masses in that region.

  2. Morphosedimentary evolution of carbonate sandy beaches at decadal scale : case study in Reunion Island , Indian Ocean

    Science.gov (United States)

    Mahabot, Marie-Myriam; Pennober, Gwenaelle; Suanez, Serge; Troadec, Roland; Delacourt, Christophe

    2017-04-01

    Global change introduce a lot of uncertainties concerning future trajectory of beaches by directly or indirectly modifying major driving factors. An improved understanding of the past shoreline evolution may help for anticipate future coastline response. However, in tropical environment, studies concerning carbonate beaches dynamics are scarce compared to open sandy beaches. Consequently, coral reef protected beaches morphological adjustment is still poorly understood and long-term evolution rate are poorly quantified in these specific environment. In this context, La Reunion Island, insular department of France located in Indian Ocean, constitute a favoured laboratory. This high volcanic island possesses 25 km of carbonate beaches which experience hydrodynamic forcing specific from tropical environment: cyclonic swell during summer and long period swell during winter. Because of degraded coral reef health and high anthropogenic pressure, 50% of the beaches are in erosion since 1970s. Beach survey has been conducted since 1990s by scientist and are now encompassed as pilot site within a French observatory network which guarantee long-term survey with high resolution observational techniques. Thus, La Reunion Island is one of the rare carbonate beach to be surveyed since 20 years. This study aims to examined and quantify beach response at decadal scale on carbonate sandy beaches of Reunion Island. The study focus on 12 km of beaches from Cap Champagne to the Passe de Trois-Bassins. The analyze of 15 beach profile data originated from historical and DGPS beach topographic data confirm long term trend to erosion. Sediment lost varies between 0.5 and 2 m3.yr-1 since 1998. However longshore current have led to accretion of some part of beach compartment with rate of 0.7 to 1.6 m3.yr-1. Wave climate was examined from in-situ measurement over 15 years and show that extreme waves associated with tropical cyclones and long period swell play a major role in beach dynamics

  3. Light absorbing organic aerosols (brown carbon) over the tropical Indian Ocean: impact of biomass burning emissions

    International Nuclear Information System (INIS)

    Srinivas, Bikkina; Sarin, M M

    2013-01-01

    The first field measurements of light absorbing water-soluble organic carbon (WSOC), referred as brown carbon (BrC), have been made in the marine atmospheric boundary layer (MABL) during the continental outflow to the Bay of Bengal (BoB) and the Arabian Sea (ARS). The absorption signal measured at 365 nm in aqueous extracts of aerosols shows a systematic linear increase with WSOC concentration, suggesting a significant contribution from BrC to the absorption properties of organic aerosols. The mass absorption coefficient (b abs ) of BrC shows an inverse hyperbolic relation with wavelength (from ∼300 to 700 nm), providing an estimate of the Angstrom exponent (α P , range: 3–19; Av: 9 ± 3). The mass absorption efficiency of brown carbon (σ abs−BrC ) in the MABL varies from 0.17 to 0.72 m 2  g −1 (Av: 0.45 ± 0.14 m 2  g −1 ). The α P and σ abs−BrC over the BoB are quite similar to that studied from a sampling site in the Indo-Gangetic Plain (IGP), suggesting the dominant impact of organic aerosols associated with the continental outflow. A comparison of the mass absorption efficiency of BrC and elemental carbon (EC) brings to focus the significant role of light absorbing organic aerosols (from biomass burning emissions) in atmospheric radiative forcing over oceanic regions located downwind of the pollution sources. (letter)

  4. Climate Change Impacts on the Organic Carbon Cycle at the Land-Ocean Interface

    Science.gov (United States)

    Canuel, E. A.; Cammer, S. S.; McIntosh, H.; Pondell, C. R.

    2012-12-01

    Humans have modified estuaries across the globe by altering the delivery of water, sediments and elements such as carbon and nitrogen that play important roles in biogeochemical processes. These activities have caused declines in the health and quality of estuarine ecosystems globally and this trend will likely continue due to increasing population growth in coastal regions, expected changes associated with climate change, and their interaction with each other, leading to serious consequences for the ecological and societal services they provide. A key function of estuaries is the transfer and transformation of carbon and biogenic elements between land and ocean systems. The anticipated effects of climate change on biogeochemical processes in estuaries are likely to be both numerous and complex but are poorly understood. Climate change has the potential to influence the carbon cycle in estuaries through anticipated changes to organic matter production, transformation, burial and export. Estuarine biogeochemical processes will likely be altered by: 1) sea level rise and increased storm intensity which will amplify the erosion and transfer of terrigenous materials, 2) increases in water temperatures which will enhance the rates of biological and biogeochemical processes (e.g., enzyme kinetics, decomposition rates, and remineralization), while simultaneously decreasing the concentration of dissolved oxygen, 3) changes in particle (or sediment) loadings in response to altered patterns of precipitation and river runoff, and 4) altered inputs of nutrients and dissolved organic materials to coastal waters, also resulting from changing precipitation and runoff. In this presentation, we review the effects of climate change on the carbon cycle in estuaries, with a focus on the temperate estuaries of North America.

  5. Ocean Biological Pump Sensitivities and Implications for Climate Change Impacts

    Science.gov (United States)

    Romanou, Anastasia

    2013-01-01

    The ocean is one of the principal reservoirs of CO2, a greenhouse gas, and therefore plays a crucial role in regulating Earth's climate. Currently, the ocean sequesters about a third of anthropogenic CO2 emissions, mitigating the human impact on climate. At the same time, the deeper ocean represents the largest carbon pool in the Earth System and processes that describe the transfer of carbon from the surface of the ocean to depth are intimately linked to the effectiveness of carbon sequestration.The ocean biological pump (OBP), which involves several biogeochemical processes, is a major pathway for transfer of carbon from the surface mixed layer into the ocean interior. About 75 of the carbon vertical gradient is due to the carbon pump with only 25 attributed to the solubility pump. However, the relative importance and role of the two pumps is poorly constrained. OBP is further divided to the organic carbon pump (soft tissue pump) and the carbonate pump, with the former exporting about 10 times more carbon than the latter through processes like remineralization.Major uncertainties about OBP, and hence in the carbon uptake and sequestration, stem from uncertainties in processes involved in OBP such as particulate organicinorganic carbon sinkingsettling, remineralization, microbial degradation of DOC and uptakegrowth rate changes of the ocean biology. The deep ocean is a major sink of atmospheric CO2 in scales of hundreds to thousands of years, but how the export efficiency (i.e. the fraction of total carbon fixation at the surface that is transported at depth) is affected by climate change remains largely undetermined. These processes affect the ocean chemistry (alkalinity, pH, DIC, particulate and dissolved organic carbon) as well as the ecology (biodiversity, functional groups and their interactions) in the ocean. It is important to have a rigorous, quantitative understanding of the uncertainties involved in the observational measurements, the models and the

  6. PISCES-v2: an ocean biogeochemical model for carbon and ecosystem studies

    Directory of Open Access Journals (Sweden)

    O. Aumont

    2015-08-01

    of marine ecosystems (phytoplankton, microzooplankton and mesozooplankton and the biogeochemical cycles of carbon and of the main nutrients (P, N, Fe, and Si. The model is intended to be used for both regional and global configurations at high or low spatial resolutions as well as for short-term (seasonal, interannual and long-term (climate change, paleoceanography analyses. There are 24 prognostic variables (tracers including two phytoplankton compartments (diatoms and nanophytoplankton, two zooplankton size classes (microzooplankton and mesozooplankton and a description of the carbonate chemistry. Formulations in PISCES-v2 are based on a mixed Monod–quota formalism. On the one hand, stoichiometry of C / N / P is fixed and growth rate of phytoplankton is limited by the external availability in N, P and Si. On the other hand, the iron and silicon quotas are variable and the growth rate of phytoplankton is limited by the internal availability in Fe. Various parameterizations can be activated in PISCES-v2, setting, for instance, the complexity of iron chemistry or the description of particulate organic materials. So far, PISCES-v2 has been coupled to the Nucleus for European Modelling of the Ocean (NEMO and Regional Ocean Modeling System (ROMS systems. A full description of PISCES-v2 and of its optional functionalities is provided here. The results of a quasi-steady-state simulation are presented and evaluated against diverse observational and satellite-derived data. Finally, some of the new functionalities of PISCES-v2 are tested in a series of sensitivity experiments.

  7. Carbon assimilation and transfer through kelp forests in the NE Atlantic is diminished under a warmer ocean climate.

    Science.gov (United States)

    Pessarrodona, Albert; Moore, Pippa J; Sayer, Martin D J; Smale, Dan A

    2018-06-03

    Global climate change is affecting carbon cycling by driving changes in primary productivity and rates of carbon fixation, release and storage within Earth's vegetated systems. There is, however, limited understanding of how carbon flow between donor and recipient habitats will respond to climatic changes. Macroalgal-dominated habitats, such as kelp forests, are gaining recognition as important carbon donors within coastal carbon cycles, yet rates of carbon assimilation and transfer through these habitats are poorly resolved. Here, we investigated the likely impacts of ocean warming on coastal carbon cycling by quantifying rates of carbon assimilation and transfer in Laminaria hyperborea kelp forests-one of the most extensive coastal vegetated habitat types in the NE Atlantic-along a latitudinal temperature gradient. Kelp forests within warm climatic regimes assimilated, on average, more than three times less carbon and donated less than half the amount of particulate carbon compared to those from cold regimes. These patterns were not related to variability in other environmental parameters. Across their wider geographical distribution, plants exhibited reduced sizes toward their warm-water equatorward range edge, further suggesting that carbon flow is reduced under warmer climates. Overall, we estimated that Laminaria hyperborea forests stored ~11.49 Tg C in living biomass and released particulate carbon at a rate of ~5.71 Tg C year -1 . This estimated flow of carbon was markedly higher than reported values for most other marine and terrestrial vegetated habitat types in Europe. Together, our observations suggest that continued warming will diminish the amount of carbon that is assimilated and transported through temperate kelp forests in NE Atlantic, with potential consequences for the coastal carbon cycle. Our findings underline the need to consider climate-driven changes in the capacity of ecosystems to fix and donate carbon when assessing the impacts of

  8. Black carbon concentrations and sources in the marine boundary layer of the tropical Atlantic Ocean using four methodologies

    Science.gov (United States)

    Combustion-derived aerosols in the marine boundary layer have been poorly studied, especially in remote environments such as the open Atlantic Ocean. The tropical Atlantic has the potential to contain a high concentration of aerosols, such as black carbon, due to the African emis...

  9. Brown Carbon Production in Ammonium- or Amine-Containing Aerosol Particles by Reactive Uptake of Methylglyoxal and Photolytic Cloud Cycling.

    Science.gov (United States)

    De Haan, David O; Hawkins, Lelia N; Welsh, Hannah G; Pednekar, Raunak; Casar, Jason R; Pennington, Elyse A; de Loera, Alexia; Jimenez, Natalie G; Symons, Michael A; Zauscher, Melanie; Pajunoja, Aki; Caponi, Lorenzo; Cazaunau, Mathieu; Formenti, Paola; Gratien, Aline; Pangui, Edouard; Doussin, Jean-François

    2017-07-05

    The effects of methylglyoxal uptake on the physical and optical properties of aerosol containing amines or ammonium sulfate were determined before and after cloud processing in a temperature- and RH-controlled chamber. The formation of brown carbon was observed upon methylglyoxal addition, detected as an increase in water-soluble organic carbon mass absorption coefficients below 370 nm and as a drop in single-scattering albedo at 450 nm. The imaginary refractive index component k 450 reached a maximum value of 0.03 ± 0.009 with aqueous glycine aerosol particles. Browning of solid particles occurred at rates limited by chamber mixing (cloud events with chamber lights on, suggesting photosensitized brown carbon formation. Despite these changes in optical aerosol characteristics, increases in dried aerosol mass were rarely observed (<1 μg/m 3 in all cases), consistent with previous experiments on methylglyoxal. Under dry, particle-free conditions, methylglyoxal reacted (presumably on chamber walls) with methylamine with a rate constant k = (9 ± 2) × 10 -17 cm 3 molecule -1 s -1 at 294 K and activation energy E a = 64 ± 37 kJ/mol.

  10. The inhibition of marine nitrification by ocean disposal of carbon dioxide

    International Nuclear Information System (INIS)

    Huesmann, M.H.; Skillman, A.D.; Crecelius, E.A.

    2002-01-01

    In an attempt to reduce the threat of global warming, it has been proposed that the rise of atmospheric carbon dioxide concentrations be reduced by the ocean disposal of CO 2 from the flue gases of fossil fuel-fired power plants. The release of large amounts of CO 2 into mid or deep ocean waters will result in large plumes of acidified seawater with pH values ranging from 6 to 8. In an effort to determine whether these CO 2 -induced pH changes have any effect on marine nitrification processes, surficial (euphotic zone) and deep (aphotic zone) seawater samples were sparged with CO 2 for varying time durations to achieve a specified pH reduction, and the rate of microbial ammonia oxidation was measured spectrophotometrically as a function of pH using an inhibitor technique. For both seawater samples taken from either the euphotic or aphotic zone, the nitrification rates dropped drastically with decreasing pH. Relative to nitrification rates in the original seawater at pH 8, nitrification rates were reduced by ca. 50% at pH 7 and more than 90% at pH 6.5. Nitrification was essentially completely inhibited at pH 6. These findings suggest that the disposal of CO 2 into mid or deep oceans will most likely result in a drastic reduction of ammonia oxidation rates within the pH plume and the concomitant accumulation of ammonia instead of nitrate. It is unlikely that ammonia will reach the high concentration levels at which marine aquatic organisms are known to be negatively affected. However, if the ammonia-rich seawater from inside the pH plume is upwelled into the euphotic zone, it is likely that changes in phytoplankton abundance and community structure will occur. Finally, the large-scale inhibition of nitrification and the subsequent reduction of nitrite and nitrate concentrations could also result in a decrease of denitrification rates which, in turn, could lead to the buildup of nitrogen and unpredictable eutrophication phenomena. Clearly, more research on the

  11. Toxicological effects of multi-walled carbon nanotubes on Saccharomyces cerevisiae: The uptake kinetics and mechanisms and the toxic responses

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Song; Zhu, Bin; Huang, Aiguo [College of Animal Science and Technology, Northwest A& F University, Yangling 712100 (China); Hu, Yang [College of Science, Northwest A& F University, Yangling 712100 (China); Wang, Gaoxue, E-mail: wanggaoxue@126.com [College of Animal Science and Technology, Northwest A& F University, Yangling 712100 (China); Ling, Fei, E-mail: feiling@nwsuaf.edu.cn [College of Animal Science and Technology, Northwest A& F University, Yangling 712100 (China)

    2016-11-15

    Highlights: • MWCNTs (<100 mg/L) were not toxic to S. cerevisiae. • MWCNTs were internalized in S. cerevisiae cells by three pathways. • The uptake kinetics and the subcellular distribution of MWCNTs in S. cerevisiae cells were shown. • S. cerevisiae cells were undergoing apoptosis by mitochondrial impairment pathway. - Abstract: Using Saccharomyces cerevisiae as an experimental model, the potential toxicological effects of oxidized multi-walled carbon nanotubes (MWCNTs) were investigated following exposure to 0–600 mg/L for 24 h. Results indicated that MWCNTs (>100 mg/L) had adverse effects on the cell proliferation. MWCNTs were clearly visible in lysosome, vacuole, endosome, mitochondria, multivesicular body and localization in the perinuclear region. The uptake kinetics data demonstrated that the maximum MWCNTs content (209.61 mg/g) was reached at 3 h, and a steady state was reached after 18 h. Based on the combined results of transmission electron microscope, endocytosis inhibition experiments and endocytosis-related genes (END3, END6, Sla2 and Rsp5) expression analysis, we elucidated MWCNTs uptake mechanism: (i) via a direct penetration of single MWCNTs; (ii) via endocytosis of single MWCNTs; and (iii) via endocytosis of MWCNTs aggregates. The percentage of apoptosis was significant increased at 600 mg/L. The decrease of mitochondrial transmembrane potential and the leakage of cytochrome c shown dose-dependent manners. Interestingly, there was no significant increase of reactive oxygen species (ROS). The apoptosis-related genes (SOD1, SOD2, Yca1, Nma111 and Nuc1) were significant changed. These results obtained in our study demonstrated that oxidized MWCNTs induce Saccharomyces cerevisiae apoptosis via mitochondrial impairment pathway.

  12. Historical carbon emissions and uptake from the agricultural frontier of the Brazilian Amazon.

    Science.gov (United States)

    Galford, Gillian L; Melillo, Jerry M; Kicklighter, David W; Mustard, John F; Cronin, Timothy W; Cerri, Carlos E P; Cerri, Carlos C

    2011-04-01

    Tropical ecosystems play a large and complex role in the global carbon cycle. Clearing of natural ecosystems for agriculture leads to large pulses of CO2 to the atmosphere from terrestrial biomass. Concurrently, the remaining intact ecosystems, especially tropical forests, may be sequestering a large amount of carbon from the atmosphere in response to global environmental changes including climate changes and an increase in atmospheric CO2. Here we use an approach that integrates census-based historical land use reconstructions, remote-sensing-based contemporary land use change analyses, and simulation modeling of terrestrial biogeochemistry to estimate the net carbon balance over the period 1901-2006 for the state of Mato Grosso, Brazil, which is one of the most rapidly changing agricultural frontiers in the world. By the end of this period, we estimate that of the state's 925 225 km2, 221 092 km2 have been converted to pastures and 89 533 km2 have been converted to croplands, with forest-to-pasture conversions being the dominant land use trajectory but with recent transitions to croplands increasing rapidly in the last decade. These conversions have led to a cumulative release of 4.8 Pg C to the atmosphere, with 80% from forest clearing and 20% from the clearing of cerrado. Over the same period, we estimate that the residual undisturbed ecosystems accumulated 0.3 Pg C in response to CO2 fertilization. Therefore, the net emissions of carbon from Mato Grosso over this period were 4.5 Pg C. Net carbon emissions from Mato Grosso since 2000 averaged 146 Tg C/yr, on the order of Brazil's fossil fuel emissions during this period. These emissions were associated with the expansion of croplands to grow soybeans. While alternative management regimes in croplands, including tillage, fertilization, and cropping patterns promote carbon storage in ecosystems, they remain a small portion of the net carbon balance for the region. This detailed accounting of a region's carbon

  13. Sorptive Uptake Studies of an Aryl-Arsenical with Iron Oxide Composites on an Activated Carbon Support

    Directory of Open Access Journals (Sweden)

    Jae H. Kwon

    2014-03-01

    Full Text Available Sorption uptake kinetics and equilibrium studies for 4-hydroxy-3-nitrobenzene arsonic acid (roxarsone was evaluated with synthetic magnetite (Mag-P, commercial magnetite (Mag-C, magnetite 10%, 19%, and 32% composite material (CM-10, -19, -32 that contains granular activated carbon (GAC, and synthetic goethite at pH 7.00 in water at 21 °C for 24 h. GAC showed the highest sorptive removal of roxarsone and the relative uptake for each sorbent material with roxarsone are listed in descending order as follows: GAC (471 mg/g > goethite (418 mg/g > CM-10 (377 mg/g CM-19 (254 mg/g > CM-32 (227 mg/g > Mag-P (132 mg/g > Mag-C (29.5 mg/g. The As (V moiety of roxarsone is adsorbed onto the surface of the iron oxide/oxyhydrate and is inferred as inner-sphere surface complexes; monodentate-mononuclear, bidentate-mononuclear, and bidentate-binuclear depending on the protolytic speciation of roxarsone. The phenyl ring of roxarsone provides the primary driving force for the sorptive interaction with the graphene surface of GAC and its composites. Thus, magnetite composites are proposed as multi-purpose adsorbents for the co-removal of inorganic and organic arsenicals due to the presence of graphenic and iron oxide active adsorption sites.

  14. Soil respiration and photosynthetic uptake of carbon dioxide by ground-cover plants in four ages of jack pine forest

    Science.gov (United States)

    Striegl, Robert G.; Wickland, K.P.

    2001-01-01

    Soil carbon dioxide (CO2) emission (soil respiration), net CO2 exchange after photosynthetic uptake by ground-cover plants, and soil CO2 concentration versus depth below land surface were measured at four ages of jack pine (Pinus banksiana Lamb.) forest in central Saskatchewan. Soil respiration was smallest at a clear-cut site, largest in an 8-year-old stand, and decreased with stand age in 20-year-old and mature (60-75 years old) stands during May-September 1994 (12.1, 34.6, 31.5, and 24.9 mol C??m-2, respectively). Simulations of soil respiration at each stand based on continuously recorded soil temperature were within one standard deviation of measured flux for 48 of 52 measurement periods, but were 10%-30% less than linear interpolations of measured flux for the season. This was probably due to decreased soil respiration at night modeled by the temperature-flux relationships, but not documented by daytime chamber measurements. CO2 uptake by ground-cover plants ranged from 0 at the clear-cut site to 29, 25, and 9% of total growing season soil respiration at the 8-year, 20-year, and mature stands. CO2 concentrations were as great as 7150 ppmv in the upper 1 m of unsaturated zone and were proportional to measured soil respiration.

  15. Spontaneous confocal Raman microscopy--a tool to study the uptake of nanoparticles and carbon nanotubes into cells

    Science.gov (United States)

    Romero, Gabriela; Rojas, Elena; Estrela-Lopis, Irina; Donath, Edwin; Moya, Sergio Enrique

    2011-06-01

    Confocal Raman microscopy as a label-free technique was applied to study the uptake and internalization of poly(lactide- co-glycolide) (PLGA) nanoparticles (NPs) and carbon nanotubes (CNTs) into hepatocarcinoma human HepG2 cells. Spontaneous confocal Raman spectra was recorded from the cells exposed to oxidized CNTs and to PLGA NPs. The Raman spectra showed bands arising from the cellular environment: lipids, proteins, nucleic acids, as well as bands characteristic for either PLGA NPs or CNTs. The simultaneous generation of Raman bands from the cell and nanomaterials from the same spot proves internalization, and also indicates the cellular region, where the nanomaterial is located. For PLGA NPs, it was found that they preferentially co-localized with lipid bodies, while the oxidized CNTs are located in the cytoplasm.

  16. Ocean Carbon and Biogeochemistry Scoping Workshop on Terrestrial and Coastal Carbon Fluxes in the Gulf of Mexico, St. Petersburg, FL, May 6-8, 2008

    Science.gov (United States)

    Robbins, L.L.; Coble, P.G.; Clayton, T.D.; Cai, W.J.

    2009-01-01

    Despite their relatively small surface area, ocean margins may have a significant impact on global biogeochemical cycles and, potentially, the global air-sea fluxes of carbon dioxide. Margins are characterized by intense geochemical and biological processing of carbon and other elements and exchange large amounts of matter and energy with the open ocean. The area-specific rates of productivity, biogeochemical cycling, and organic/inorganic matter sequestration are high in coastal margins, with as much as half of the global integrated new production occurring over the continental shelves and slopes (Walsh, 1991; Doney and Hood, 2002; Jahnke, in press). However, the current lack of knowledge and understanding of biogeochemical processes occurring at the ocean margins has left them largely ignored in most of the previous global assessments of the oceanic carbon cycle (Doney and Hood, 2002). A major source of North American and global uncertainty is the Gulf of Mexico, a large semi-enclosed subtropical basin bordered by the United States, Mexico, and Cuba. Like many of the marginal oceans worldwide, the Gulf of Mexico remains largely unsampled and poorly characterized in terms of its air-sea exchange of carbon dioxide and other carbon fluxes. In May 2008, the Ocean Carbon and Biogeochemistry Scoping Workshop on Terrestrial and Coastal Carbon Fluxes in the Gulf of Mexico was held in St. Petersburg, FL, to address the information gaps of carbon fluxes associated with the Gulf of Mexico and to offer recommendations to guide future research. The meeting was attended by over 90 participants from over 50 U.S. and Mexican institutions and agencies. The Ocean Carbon and Biogeochemistry program (OCB; http://www.us-ocb.org/) sponsored this workshop with support from the National Science Foundation, the National Oceanic and Atmospheric Administration, the National Aeronautics and Space Administration, the U.S. Geological Survey, and the University of South Florida. The goal of

  17. Simulated Impact of Glacial Runoff on CO2 Uptake in the Gulf of Alaska

    Science.gov (United States)

    Pilcher, Darren J.; Siedlecki, Samantha A.; Hermann, Albert J.; Coyle, Kenneth O.; Mathis, Jeremy T.; Evans, Wiley

    2018-01-01

    The Gulf of Alaska (GOA) receives substantial summer freshwater runoff from glacial meltwater. The alkalinity of this runoff is highly dependent on the glacial source and can modify the coastal carbon cycle. We use a regional ocean biogeochemical model to simulate CO2 uptake in the GOA under different alkalinity-loading scenarios. The GOA is identified as a current net sink of carbon, though low-alkalinity tidewater glacial runoff suppresses summer coastal carbon uptake. Our model shows that increasing the alkalinity generates an increase in annual CO2 uptake of 1.9-2.7 TgC/yr. This transition is comparable to a projected change in glacial runoff composition (i.e., from tidewater to land-terminating) due to continued climate warming. Our results demonstrate an important local carbon-climate feedback that can significantly increase coastal carbon uptake via enhanced air-sea exchange, with potential implications to the coastal ecosystems in glaciated areas around the world.

  18. Can frequent precipitation moderate drought impact on peatmoss carbon uptake in northern peatlands?

    NARCIS (Netherlands)

    Nijp, J.J.; Limpens, J.; Metselaar, K.; Zee, van der S.E.A.T.M.; Berendse, F.; Robroek, B.J.M.

    2015-01-01

    Northern peatlands represent a large global carbon store that potentially can be destabilised by summer water table drawdown. Precipitation can moderate negative impacts of water table drawdown by rewetting peatmoss (Sphagnum spp.), the ecosystems’ key species. Yet, the frequency for such rewetting

  19. Can frequent precipitation moderate the impact of drought on peatmoss carbon uptake in northern peatlands?

    NARCIS (Netherlands)

    Nijp, J.J.; Limpens, J.; Metselaar, K.; Zee, van der S.E.A.T.M.; Berendse, F.; Robroek, B.J.M.

    2014-01-01

    Northern peatlands represent a large global carbon store that can potentially be destabilized by summer water table drawdown. Precipitation can moderate the negative impacts of water table drawdown by rewetting peatmoss (Sphagnum spp.), the ecosystem's key species. Yet, the frequency of such

  20. How much primary coastal temperate rain forest should society retain? Carbon uptake, recreation and other values

    NARCIS (Netherlands)

    Kooten, van G.C.; Bulte, E.H.

    2000-01-01

    In this study, average and marginal approaches for determining optimal preservation of primary forests on British Columbia's coast are compared. When the market values from timber, mushrooms, etc., and nonmarket benefits (e.g., carbon sink, preservation values) of preserving old-growth forests are

  1. Terrestrial gross carbon dioxide uptake : Global distribution and covariation with climate

    NARCIS (Netherlands)

    Beer, Christian; Reichstein, Markus; Tomelleri, Enrico; Ciais, Philippe; Jung, Martin; Carvalhais, Nuno; Rödenbeck, Christian; Arain, M. Altaf; Baldocchi, Dennis D.; Bonan, Gordon B.; Bondeau, Alberte; Cescatti, Alessandro; Lasslop, Gitta; Lindroth, Anders; Lomas, Mark; Luyssaert, Sebastiaan; Margolis, Hank; Oleson, Keith W.; Roupsard, Olivier; Veenendaal, Elmar; Viovy, Nicolas; Williams, Christopher M.; Woodward, F. Ian; Papale, Dario

    2010-01-01

    Terrestrial gross primary production (GPP) is the largest global CO 2 flux driving several ecosystem functions. We provide an observation-based estimate of this flux at 123 ± 8 petagrams of carbon per year (Pg C year-1) using eddy covariance flux data and various diagnostic models. Tropical forests

  2. High carbon dioxide uptake by subtropical forest ecosystems in the East Asian monsoon region

    Science.gov (United States)

    Yu, Guirui; Chen, Zhi; Piao, Shilong; Peng, Changhui; Ciais, Philippe; Wang, Qiufeng; Li, Xuanran; Zhu, Xianjin

    2014-01-01

    Temperate- and high-latitude forests have been shown to contribute a carbon sink in the Northern Hemisphere, but fewer studies have addressed the carbon balance of the subtropical forests. In the present study, we integrated eddy covariance observations established in the 1990s and 2000s to show that East Asian monsoon subtropical forests between 20°N and 40°N represent an average net ecosystem productivity (NEP) of 362 ± 39 g C m−2 yr−1 (mean ± 1 SE). This average forest NEP value is higher than that of Asian tropical and temperate forests and is also higher than that of forests at the same latitudes in Europe–Africa and North America. East Asian monsoon subtropical forests have comparable NEP to that of subtropical forests of the southeastern United States and intensively managed Western European forests. The total NEP of East Asian monsoon subtropical forests was estimated to be 0.72 ± 0.08 Pg C yr−1, which accounts for 8% of the global forest NEP. This result indicates that the role of subtropical forests in the current global carbon cycle cannot be ignored and that the regional distributions of the Northern Hemisphere's terrestrial carbon sinks are needed to be reevaluated. The young stand ages and high nitrogen deposition, coupled with sufficient and synchronous water and heat availability, may be the primary reasons for the high NEP of this region, and further studies are needed to quantify the contribution of each underlying factor. PMID:24639529

  3. Carbon availability triggers fungal nitrogen uptake and transport in arbuscular mycorrhizal symbiosis.

    NARCIS (Netherlands)

    Fellbaum, C.R.; Gachomo, E.W.; Beesetty, Y.; Choudhari, S.; Strahan, G.D.; Pfeffer, P.E.; Kiers, E.T.; Bücking, H.

    2012-01-01

    The arbuscular mycorrhizal (AM) symbiosis, formed between the majority of land plants and ubiquitous soil fungi of the phylum Glomeromycota, is responsible for massive nutrient transfer and global carbon sequestration. AM fungi take up nutrients from the soil and exchange them against

  4. Cycling of organic carbon in the ocean: use of naturally occuring radiocarbon as a long and short term tracer

    International Nuclear Information System (INIS)

    Williams, P.M.; Linick, T.W.

    1975-01-01

    The natural radiocarbon activities of surface, bathypelagic and benthic marine organisms have been measured for samples collected from the north central, north eastern and central equatorial Pacific Ocean and from the Ross Sea in Antarctica. These measurements show that 1961-1962 bomb-carbon-14 has been incorporated into the bathypelagic specimens in varying amounts. Thus, pollutants introduced into surface waters of the oceans may be removed more or less rapidly from the euphotic zone into the deep water depending upon particular food chain mechanisms. These results are discussed in relation to the cycling of disolved organic carbon, the flux of particulate organic carbon through the seawater column into the sediments, and to the oxidation rates of organic matter in the deep sea. (author)

  5. Tropical seagrass meadows modify seawater carbon chemistry: implications for coral reefs impacted by ocean acidification

    International Nuclear Information System (INIS)

    Unsworth, Richard K F; Collier, Catherine J; Henderson, Gideon M; McKenzie, Len J

    2012-01-01

    Highly productive tropical seagrasses often live adjacent to or among coral reefs and utilize large amounts of inorganic carbon. In this study, the effect of seagrass productivity on seawater carbonate chemistry and coral calcification was modelled on the basis of an analysis of published data. Published data (11 studies, 64 records) reveal that seagrass meadows in the Indo-Pacific have an 83% chance of being net autotrophic, resulting in an average net sink of 155 gC m −2 yr −1 . The capacities for seagrass productivity were analysed using an empirical model to examine the effect on seawater carbonate chemistry. Our analyses indicate that increases in pH of up to 0.38 units, and Ω arag increases of 2.9 are possible in the presence of seagrass meadows (compared to their absence) with the precise values of these increases dependent on water residence time (tidal flushing) and water depth. In shallow water reef environments, Scleractinian coral calcification downstream of seagrass has the potential to be ≈18% greater than in an environment without seagrass. If this potential benefit to reef calcifiers is supported by further study it offers a potential tool in marine park management at a local scale. The applicability of this will depend upon local physical conditions as well as the spatial configuration of habitats, and the factors that influence their productivity. This novel study suggests that, in addition to their importance to fisheries, sediment stabilization and primary production, seagrass meadows may enhance coral reef resilience to future ocean acidification. (letter)

  6. Deepwater carbonate ion concentrations in the western tropical Pacific since 250 ka: Evidence for oceanic carbon storage and global climate influence

    Science.gov (United States)

    Qin, Bingbin; Li, Tiegang; Xiong, Zhifang; Algeo, Thomas J.; Chang, Fengming

    2017-04-01

    We present new "size-normalized weight" (SNW)-Δ[CO32-] core-top calibrations for three planktonic foraminiferal species and assess their reliability as a paleo-alkalinity proxy. SNWs of Globigerina sacculifer and Neogloboquadrina dutertrei can be used to reconstruct past deep Pacific [CO32-], whereas SNWs of Pulleniatina obliquiloculata are controlled by additional environmental factors. Based on this methodological advance, we reconstruct SNW-based deepwater [CO32-] for core WP7 from the western tropical Pacific since 250 ka. Secular variation in the SNW proxy documents little change in deep Pacific [CO32-] between the Last Glacial Maximum and the Holocene. Further back in time, deepwater [CO32-] shows long-term increases from marine isotope stage (MIS) 5e to MIS 3 and from early MIS 7 to late MIS 6, consistent with the "coral reef hypothesis" that the deep Pacific Ocean carbonate system responded to declining shelf carbonate production during these two intervals. During deglaciations, we have evidence of [CO32-] peaks coincident with Terminations 2 and 3, which suggests that a breakdown of oceanic vertical stratification drove a net transfer of CO2 from the ocean to the atmosphere, causing spikes in carbonate preservation (i.e., the "deglacial ventilation hypothesis"). During MIS 4, a transient decline in SNW-based [CO32-], along with other reported [CO32-] and/or dissolution records, implies that increased deep-ocean carbon storage resulted in a global carbonate dissolution event. These findings provide new insights into the role of the deep Pacific in the global carbon cycle during the late Quaternary.

  7. Complementary constraints from carbon (13C) and nitrogen (15N) isotopes on the glacial ocean's soft-tissue biological pump

    Science.gov (United States)

    Schmittner, A.; Somes, C. J.

    2016-06-01

    A three-dimensional, process-based model of the ocean's carbon and nitrogen cycles, including 13C and 15N isotopes, is used to explore effects of idealized changes in the soft-tissue biological pump. Results are presented from one preindustrial control run (piCtrl) and six simulations of the Last Glacial Maximum (LGM) with increasing values of the spatially constant maximum phytoplankton growth rate μmax, which accelerates biological nutrient utilization mimicking iron fertilization. The default LGM simulation, without increasing μmax and with a shallower and weaker Atlantic Meridional Overturning Circulation and increased sea ice cover, leads to 280 Pg more respired organic carbon (Corg) storage in the deep ocean with respect to piCtrl. Dissolved oxygen concentrations in the colder glacial thermocline increase, which reduces water column denitrification and, with delay, nitrogen fixation, thus increasing the ocean's fixed nitrogen inventory and decreasing δ15NNO3 almost everywhere. This simulation already fits sediment reconstructions of carbon and nitrogen isotopes relatively well, but it overestimates deep ocean δ13CDIC and underestimates δ15NNO3 at high latitudes. Increasing μmax enhances Corg and lowers deep ocean δ13CDIC, improving the agreement with sediment data. In the model's Antarctic and North Pacific Oceans modest increases in μmax result in higher δ15NNO3 due to enhanced local nutrient utilization, improving the agreement with reconstructions there. Models with moderately increased μmax fit both isotope data best, whereas large increases in nutrient utilization are inconsistent with nitrogen isotopes although they still fit the carbon isotopes reasonably well. The best fitting models reproduce major features of the glacial δ13CDIC, δ15N, and oxygen reconstructions while simulating increased Corg by 510-670 Pg compared with the preindustrial ocean. These results are consistent with the idea that the soft-tissue pump was more efficient

  8. Sulfur and carbon geochemistry of the Santa Elena peridotites: Comparing oceanic and continental processes during peridotite alteration

    Science.gov (United States)

    Schwarzenbach, Esther M.; Gill, Benjamin C.; Gazel, Esteban; Madrigal, Pilar

    2016-05-01

    Ultramafic rocks exposed on the continent serve as a window into oceanic and continental processes of water-peridotite interaction, so called serpentinization. In both environments there are active carbon and sulfur cycles that contain abiogenic and biogenic processes, which are eventually imprinted in the geochemical signatures of the basement rocks and the calcite and magnesite deposits associated with fluids that issue from these systems. Here, we present the carbon and sulfur geochemistry of ultramafic rocks and carbonate deposits from the Santa Elena ophiolite in Costa Rica. The aim of this study is to leverage the geochemistry of the ultramafic sequence and associated deposits to distinguish between processes that were dominant during ocean floor alteration and those dominant during low-temperature, continental water-peridotite interaction. The peridotites are variably serpentinized with total sulfur concentrations up to 877 ppm that is typically dominated by sulfide over sulfate. With the exception of one sample the ultramafic rocks are characterized by positive δ34Ssulfide (up to + 23.1‰) and δ34Ssulfate values (up to + 35.0‰). Carbon contents in the peridotites are low and are isotopically distinct from typical oceanic serpentinites. In particular, δ13C of the inorganic carbon suggests that the carbon is not derived from seawater, but rather the product of the interaction of meteoric water with the ultramafic rocks. In contrast, the sulfur isotope data from sulfide minerals in the peridotites preserve evidence for interaction with a hydrothermal fluid. Specifically, they indicate closed system abiogenic sulfate reduction suggesting that oceanic serpentinization occurred with limited input of seawater. Overall, the geochemical signatures preserve evidence for both oceanic and continental water-rock interaction with the majority of carbon (and possibly sulfate) being incorporated during continental water-rock interaction. Furthermore, there is

  9. Carbon: Nitrogen Interaction Regulates Expression of Genes Involved in N-Uptake and Assimilation in Brassica juncea L.

    Directory of Open Access Journals (Sweden)

    Parul Goel

    Full Text Available In plants, several cellular and metabolic pathways interact with each other to regulate processes that are vital for their growth and development. Carbon (C and Nitrogen (N are two main nutrients for plants and coordination of C and N pathways is an important factor for maintaining plant growth and development. In the present work, influence of nitrogen and sucrose (C source on growth parameters and expression of genes involved in nitrogen transport and assimilatory pathways was studied in B. juncea seedlings. For this, B. juncea seedlings were treated with four combinations of C and N source viz., N source alone (-Suc+N, C source alone (+Suc-N, with N and C source (+Suc+N or without N and C source (-Suc-N. Cotyledon size and shoot length were found to be increased in seedlings, when nitrogen alone was present in the medium. Distinct expression pattern of genes in both, root and shoot tissues was observed in response to exogenously supplied N and C. The presence or depletion of nitrogen alone in the medium leads to severe up- or down-regulation of key genes involved in N-uptake and transport (BjNRT1.1, BjNRT1.8 in root tissue and genes involved in nitrate reduction (BjNR1 and BjNR2 in shoot tissue. Moreover, expression of several genes, like BjAMT1.2, BjAMT2 and BjPK in root and two genes BjAMT2 and BjGS1.1 in shoot were found to be regulated only when C source was present in the medium. Majority of genes were found to respond in root and shoot tissues, when both C and N source were present in the medium, thus reflecting their importance as a signal in regulating expression of genes involved in N-uptake and assimilation. The present work provides insight into the regulation of genes of N-uptake and assimilatory pathway in B. juncea by interaction of both carbon and nitrogen.

  10. Carbon: Nitrogen Interaction Regulates Expression of Genes Involved in N-Uptake and Assimilation in Brassica juncea L.

    Science.gov (United States)

    Goel, Parul; Bhuria, Monika; Kaushal, Mamta

    2016-01-01

    In plants, several cellular and metabolic pathways interact with each other to regulate processes that are vital for their growth and development. Carbon (C) and Nitrogen (N) are two main nutrients for plants and coordination of C and N pathways is an important factor for maintaining plant growth and development. In the present work, influence of nitrogen and sucrose (C source) on growth parameters and expression of genes involved in nitrogen transport and assimilatory pathways was studied in B. juncea seedlings. For this, B. juncea seedlings were treated with four combinations of C and N source viz., N source alone (-Suc+N), C source alone (+Suc-N), with N and C source (+Suc+N) or without N and C source (-Suc-N). Cotyledon size and shoot length were found to be increased in seedlings, when nitrogen alone was present in the medium. Distinct expression pattern of genes in both, root and shoot tissues was observed in response to exogenously supplied N and C. The presence or depletion of nitrogen alone in the medium leads to severe up- or down-regulation of key genes involved in N-uptake and transport (BjNRT1.1, BjNRT1.8) in root tissue and genes involved in nitrate reduction (BjNR1 and BjNR2) in shoot tissue. Moreover, expression of several genes, like BjAMT1.2, BjAMT2 and BjPK in root and two genes BjAMT2 and BjGS1.1 in shoot were found to be regulated only when C source was present in the medium. Majority of genes were found to respond in root and shoot tissues, when both C and N source were present in the medium, thus reflecting their importance as a signal in regulating expression of genes involved in N-uptake and assimilation. The present work provides insight into the regulation of genes of N-uptake and assimilatory pathway in B. juncea by interaction of both carbon and nitrogen. PMID:27637072

  11. Oxygenated volatile organic carbon in the western Pacific convective center: ocean cycling, air-sea gas exchange and atmospheric transport

    Science.gov (United States)

    Schlundt, Cathleen; Tegtmeier, Susann; Lennartz, Sinikka T.; Bracher, Astrid; Cheah, Wee; Krüger, Kirstin; Quack, Birgit; Marandino, Christa A.

    2017-09-01

    A suite of oxygenated volatile organic compounds (OVOCs - acetaldehyde, acetone, propanal, butanal and butanone) were measured concurrently in the surface water and atmosphere of the South China Sea and Sulu Sea in November 2011. A strong correlation was observed between all OVOC concentrations in the surface seawater along the entire cruise track, except for acetaldehyde, suggesting similar sources and sinks in the surface ocean. Additionally, several phytoplankton groups, such as haptophytes or pelagophytes, were also correlated to all OVOCs, indicating that phytoplankton may be an important source of marine OVOCs in the South China and Sulu seas. Humic- and protein-like fluorescent dissolved organic matter (FDOM) components seemed to be additional precursors for butanone and acetaldehyde. The measurement-inferred OVOC fluxes generally showed an uptake of atmospheric OVOCs by the ocean for all gases, except for butanal. A few important exceptions were found along the Borneo coast, where OVOC fluxes from the ocean to the atmosphere were inferred. The atmospheric OVOC mixing ratios over the northern coast of Borneo were relatively high compared with literature values, suggesting that this coastal region is a local hotspot for atmospheric OVOCs. The calculated amount of OVOCs entrained into the ocean seemed to be an important source of OVOCs to the surface ocean. When the fluxes were out of the ocean, marine OVOCs were found to be enough to control the locally measured OVOC distribution in the atmosphere. Based on our model calculations, at least 0.4 ppb of marine-derived acetone and butanone can reach the upper troposphere, where they may have an important influence on hydrogen oxide radical formation over the western Pacific Ocean.

  12. Uncertainties in carbon residence time and NPP-driven carbon uptake in terrestrial ecosystems of the conterminous USA: a Bayesian approach

    Directory of Open Access Journals (Sweden)

    Xuhui Zhou

    2012-10-01

    Full Text Available Carbon (C residence time is one of the key factors that determine the capacity of ecosystem C storage. However, its uncertainties have not been well quantified, especially at regional scales. Assessing uncertainties of C residence time is thus crucial for an improved understanding of terrestrial C sequestration. In this study, the Bayesian inversion and Markov Chain Monte Carlo (MCMC technique were applied to a regional terrestrial ecosystem (TECO-R model to quantify C residence times and net primary productivity (NPP-driven ecosystem C uptake and assess their uncertainties in the conterminous USA. The uncertainty was represented by coefficient of variation (CV. The 13 spatially distributed data sets of C pools and fluxes have been used to constrain TECO-R model for each biome (totally eight biomes. Our results showed that estimated ecosystem C residence times ranged from 16.6±1.8 (cropland to 85.9±15.3 yr (evergreen needleleaf forest with an average of 56.8±8.8 yr in the conterminous USA. The ecosystem C residence times and their CV were spatially heterogeneous and varied with vegetation types and climate conditions. Large uncertainties appeared in the southern and eastern USA. Driven by NPP changes from 1982 to 1998, terrestrial ecosystems in the conterminous USA would absorb 0.20±0.06 Pg C yr−1. Their spatial pattern was closely related to the greenness map in the summer with larger uptake in central and southeast regions. The lack of data or timescale mismatching between the available data and the estimated parameters lead to uncertainties in the estimated C residence times, which together with initial NPP resulted in the uncertainties in the estimated NPP-driven C uptake. The Bayesian approach with MCMC inversion provides an effective tool to estimate spatially distributed C residence time and assess their uncertainties in the conterminous USA.

  13. Climate warming feedback from mountain birch forest expansion: reduced albedo dominates carbon uptake.

    Science.gov (United States)

    de Wit, Heleen A; Bryn, Anders; Hofgaard, Annika; Karstensen, Jonas; Kvalevåg, Maria M; Peters, Glen P

    2014-07-01

    Expanding high-elevation and high-latitude forest has contrasting climate feedbacks through carbon sequestration (cooling) and reduced surface reflectance (warming), which are yet poorly quantified. Here, we present an empirically based projection of mountain birch forest expansion in south-central Norway under climate change and absence of land use. Climate effects of carbon sequestration and albedo change are compared using four emission metrics. Forest expansion was modeled for a projected 2.6 °C increase in summer temperature in 2100, with associated reduced snow cover. We find that the current (year 2000) forest line of the region is circa 100 m lower than its climatic potential due to land-use history. In the future scenarios, forest cover increased from 12% to 27% between 2000 and 2100, resulting in a 59% increase in biomass carbon storage and an albedo change from 0.46 to 0.30. Forest expansion in 2100 was behind its climatic potential, forest migration rates being the primary limiting factor. In 2100, the warming caused by lower albedo from expanding forest was 10 to 17 times stronger than the cooling effect from carbon sequestration for all emission metrics considered. Reduced snow cover further exacerbated the net warming feedback. The warming effect is considerably stronger than previously reported for boreal forest cover, because of the typically low biomass density in mountain forests and the large changes in albedo of snow-covered tundra areas. The positive climate feedback of high-latitude and high-elevation expanding forests with seasonal snow cover exceeds those of afforestation at lower elevation, and calls for further attention of both modelers and empiricists. The inclusion and upscaling of these climate feedbacks from mountain forests into global models is warranted to assess the potential global impacts. © 2013 John Wiley & Sons Ltd.

  14. Spectral Indices to Monitor Nitrogen-Driven Carbon Uptake in Field Corn

    Science.gov (United States)

    Corp, Lawrence A.; Middleton, Elizabeth M.; Campbell, Peya E.; Huemmrich, K. Fred; Daughtry, Craig S. T.; Russ, Andrew; Cheng, Yen-Ben

    2010-01-01

    Climate change is heavily impacted by changing vegetation cover and productivity with large scale monitoring of vegetation only possible with remote sensing techniques. The goal of this effort was to evaluate existing reflectance (R) spectroscopic methods for determining vegetation parameters related to photosynthetic function and carbon (C) dynamics in plants. Since nitrogen (N) is a key constituent of photosynthetic pigments and C fixing enzymes, biological C sequestration is regulated in part by N availability. Spectral R information was obtained from field corn grown at four N application rates (0, 70, 140, 280 kg N/ha). A hierarchy of spectral observations were obtained: leaf and canopy with a spectral radiometer; aircraft with the AISA sensor; and satellite with EO-1 Hyperion. A number of spectral R indices were calculated from these hyperspectral observations and compared to geo-located biophysical measures of plant growth and physiological condition. Top performing indices included the R derivative index D730/D705 and the normalized difference of R750 vs. R705 (ND705), both of which differentiated three of the four N fertilization rates at multiple observation levels and yielded high correlations to these carbon parameters: light use efficiency (LUE); C:N ratio; and crop grain yield. These results advocate the use of hyperspectral sensors for remotely monitoring carbon cycle dynamics in managed terrestrial ecosystems.

  15. Uptake of dissolved organic carbon and trace elements by zebra mussels

    Science.gov (United States)

    Roditi, Hudson A.; Fisher, Nicholas S.; Sañudo-Wilhelmy, Sergio A.

    2000-09-01

    Zebra mussels (Dreissena polymorpha) are widespread and abundant in major freshwater ecosystems in North America, even though the phytoplankton food resources in some of these systems seem to be too low to sustain them. Because phytoplankton biomass is greatly depleted in ecosystems with large D. polymorpha populations and bacteria do not seem to be an important food source for this species, exploitation of alternative carbon sources may explain the unexpected success of D. polymorpha in such environments. Here we examine the possibility that absorption of dissolved organic carbon (DOC) from water could provide a nutritional supplement to zebra mussels. We find that mussels absorb 14C-labelled DOC produced by cultured diatoms with an efficiency of 0.23%; this indicates that DOC in natural waters could contribute up to 50% of the carbon demand of zebra mussels. We also find that zebra mussels absorb some dissolved metals that have been complexed by the DOM; although absorption of dissolved selenium was unaffected by DOC, absorption of dissolved cadmium, silver and mercury by the mussels increased 32-, 8.7- and 3.6-fold, respectively, in the presence of high-molecular-weight DOC.

  16. Relevance of octanol-water distribution measurements to the potential ecological uptake of multi-walled carbon nanotubes.

    Science.gov (United States)

    Petersen, Elijah J; Huang, Qingguo; Weber, Walter J

    2010-05-01

    Many potential applications of carbon nanotubes (CNTs) require various physicochemical modifications prior to use, suggesting that nanotubes having varied properties may pose risks in ecosystems. A means for estimating bioaccumulation potentials of variously modified CNTs for incorporation in predictive fate models would be highly valuable. An approach commonly used for sparingly soluble organic contaminants, and previously suggested for use as well with carbonaceous nanomaterials, involves measurement of their octanol-water partitioning coefficient (KOW) values. To test the applicability of this approach, a methodology was developed to measure apparent octanol-water distribution behaviors for purified multi-walled carbon nanotubes and those acid treated. Substantial differences in apparent distribution coefficients between the two types of CNTs were observed, but these differences did not influence accumulation by either earthworms (Eisenia foetida) or oligochaetes (Lumbriculus variegatus), both of which showed minimal nanotube uptake for both types of nanotubes. The results suggest that traditional distribution behavior-based KOW approaches are likely not appropriate for predicting CNT bioaccumulation. Copyright (c) 2010 SETAC.

  17. Variability of the carbonate chemistry in a shallow, seagrass-dominated ecosystem: implications for ocean acidification experiments

    Science.gov (United States)

    Challener, Roberta; Robbins, Lisa L.; Mcclintock, James B.

    2016-01-01

    Open ocean observations have shown that increasing levels of anthropogenically derived atmospheric CO2 are causing acidification of the world's oceans. Yet little is known about coastal acidification and studies are just beginning to characterise the carbonate chemistry of shallow, nearshore zones where many ecologically and economically important organisms occur. We characterised the carbonate chemistry of seawater within an area dominated by seagrass beds (Saint Joseph Bay, Florida) to determine the extent of variation in pH and pCO2 over monthly and daily timescales. Distinct diel and seasonal fluctuations were observed at daily and monthly timescales respectively, indicating the influence of photosynthetic and respiratory processes on the local carbonate chemistry. Over the course of a year, the range in monthly values of pH (7.36-8.28), aragonite saturation state (0.65-5.63), and calculated pCO2 (195-2537 μatm) were significant. When sampled on a daily basis the range in pH (7.70-8.06), aragonite saturation state (1.86-3.85), and calculated pCO2 (379-1019 μatm) also exhibited significant range and indicated variation between timescales. The results of this study have significant implications for the design of ocean acidification experiments where nearshore species are utilised and indicate that coastal species are experiencing far greater fluctuations in carbonate chemistry than previously thought.

  18. Carbon and nitrogen uptake of calcareous benthic foraminifera along a depth-related oxygen gradient in the OMZ of the Arabian Sea

    Directory of Open Access Journals (Sweden)

    Annekatrin Julie Enge

    2016-02-01

    Full Text Available Foraminifera are an important faunal element of the benthos in oxygen-depleted settings such as Oxygen Minimum Zones (OMZs where they can play a relevant role in the processing of phytodetritus. We investigated the uptake of phytodetritus (labeled with 13C and 15N by cal-careous foraminifera in the 0-1 cm sediment horizon under different oxygen concentrations within the OMZ in the eastern Arabian Sea. The in situ tracer experiments were carried out along a depth transect on the Indian margin over a period of 4 to 10 days. The uptake of phy-todetrital carbon within 4 days by all investigated species shows that phytodetritus is a rele-vant food source for foraminifera in OMZ sediments. The decrease of total carbon uptake from 540 to 1100 m suggests a higher demand for carbon by species in the low-oxygen core region of the OMZ or less food competition with macrofauna. Especially Uvigerinids showed high uptake of phytodetrital carbon at the lowest oxygenated site. Variation in the ratio of phytodetrital carbon to nitrogen between species and sites indicates that foraminiferal carbon and nitrogen use can be decoupled and different nutritional demands are found between spe-cies. Lower ratio of phytodetrital carbon and nitrogen at 540 m could hint for greater demand or storage of food-based nitrogen, ingestion or hosting of bacteria under almost anoxic condi-tions. Shifts in the foraminiferal assemblage structure (controlled by oxygen or food availabil-ity and in the presence of other benthic organisms account for observed changes in the pro-cessing of phytodetritus in the different OMZ habitats. Foraminifera dominate the short-term processing of phytodetritus in the OMZ core but are less important in the lower OMZ bounda-ry region of the Indian margin as biological interactions and species distribution of foraminif-era change with depth and oxygen levels.

  19. Sedimentary evidence for enhanced hydrological cycling in response to rapid carbon release during the early Toarcian oceanic anoxic event

    Science.gov (United States)

    Izumi, Kentaro; Kemp, David B.; Itamiya, Shoma; Inui, Mutsuko

    2018-01-01

    A pronounced excursion in the carbon-isotope composition of biospheric carbon and coeval seawater warming during the early Toarcian (∼183 Ma) has been linked to the large-scale transfer of 12C-enriched carbon to the oceans and atmosphere. A European bias in the distribution of available data means that the precise pattern, tempo and global expression of this carbon cycle perturbation, and the associated environmental responses, remain uncertain. Here, we present a new cm-scale terrestrial-dominated carbon-isotope record through an expanded lower Toarcian section from Japan that displays a negative excursion pattern similar to marine and terrestrial carbon-isotope records documented from Europe. These new data suggest that 12C-enriched carbon was added to the biosphere in at least one rapid, millennial-scale pulse. Sedimentological analysis indicates a close association between the carbon-isotope excursion and high-energy sediment transport and enhanced fluvial discharge. Together, these data support the hypothesis that a sudden strengthening of the global hydrological cycle occurred in direct and immediate response to rapid carbon release and atmospheric warming.

  20. Enhanced ocean carbon storage from anaerobic alkalinity generation in coastal sediments

    NARCIS (Netherlands)

    Thomas, H.; Schiettecatte, L.-S.; Suykens, K.; Koné, Y.J.M.; Shadwick, E.H.; Prowe, A.E.F.; Bozec, Y.; Baar, H.J.W. de; Borges, A.V.; Slomp, C.

    2009-01-01

    The coastal ocean is a crucial link between land, the open ocean and the atmosphere. The shallowness of the water column permits close interactions between the sedimentary, aquatic and atmospheric compartments, which otherwise are decoupled at long time scales (≅ 1000 yr) in the open oceans. Despite

  1. Biogenic silica and organic carbon in sediments from the Pacific sector of the Southern Ocean

    International Nuclear Information System (INIS)

    Giglio, F.; Langone, L.; Morigi, C.; Frignani, M.; Ravaioli, M.

    2002-01-01

    Four cores, collected during the 1995/96 Italian Antarctic cruise and located north and south of the Polar Front, provided both qualitative and quantitative information about changes of the sediment settings driven by climate changes. Biogenic silica and organic carbon flux variations and sedimentological analyses allow us to make inferences about the fluctuation of the Polar Front during the last climate cycles: the records of our cores Anta96-1 and Anta96-16 account for fluctuations of the Polar Front of at least 5 degrees with respect to the present position, with a concomitant movement of the Marginal Ice Zone. The very low accumulation rates at the study sites are probably due to the scarce availability of micronutrients. In the area south of the Polar Front, sediment accumulation, after a decrease, appears constant during the last 250,000 yr. A subdivision in glacial/interglacial stages has been proposed, which permits the identification of the warm stage 11, which is particularly important in the Southern Ocean. (author). 13 refs., 5 figs

  2. Coral reef calcifiers buffer their response to ocean acidification using both bicarbonate and carbonate.

    Science.gov (United States)

    Comeau, S; Carpenter, R C; Edmunds, P J

    2013-02-22

    Central to evaluating the effects of ocean acidification (OA) on coral reefs is understanding how calcification is affected by the dissolution of CO(2) in sea water, which causes declines in carbonate ion concentration [CO(3)(2-)] and increases in bicarbonate ion concentration [HCO(3)(-)]. To address this topic, we manipulated [CO(3)(2-)] and [HCO(3)(-)] to test the effects on calcification of the coral Porites rus and the alga Hydrolithon onkodes, measured from the start to the end of a 15-day incubation, as well as in the day and night. [CO(3)(2-)] played a significant role in light and dark calcification of P. rus, whereas [HCO(3)(-)] mainly affected calcification in the light. Both [CO(3)(2-)] and [HCO(3)(-)] had a significant effect on the calcification of H. onkodes, but the strongest relationship was found with [CO(3)(2-)]. Our results show that the negative effect of declining [CO(3)(2-)] on the calcification of corals and algae can be partly mitigated by the use of HCO(3)(-) for calcification and perhaps photosynthesis. These results add empirical support to two conceptual models that can form a template for further research to account for the calcification response of corals and crustose coralline algae to OA.

  3. An Ocean Acidification Acclimatised Green Tide Alga Is Robust to Changes of Seawater Carbon Chemistry but Vulnerable to Light Stress.

    Directory of Open Access Journals (Sweden)

    Guang Gao

    Full Text Available Ulva is the dominant genus in the green tide events and is considered to have efficient CO2 concentrating mechanisms (CCMs. However, little is understood regarding the impacts of ocean acidification on the CCMs of Ulva and the consequences of thalli's acclimation to ocean acidification in terms of responding to environmental factors. Here, we grew a cosmopolitan green alga, Ulva linza at ambient (LC and elevated (HC CO2 levels and investigated the alteration of CCMs in U. linza grown at HC and its responses to the changed seawater carbon chemistry and light intensity. The inhibitors experiment for photosynthetic inorganic carbon utilization demonstrated that acidic compartments, extracellular carbonic anhydrase (CA and intracellular CA worked together in the thalli grown at LC and the acquisition of exogenous carbon source in the thalli could be attributed to the collaboration of acidic compartments and extracellular CA. Contrastingly, when U. linza was grown at HC, extracellular CA was completely inhibited, acidic compartments and intracellular CA were also down-regulated to different extents and thus the acquisition of exogenous carbon source solely relied on acidic compartments. The down-regulated CCMs in U. linza did not affect its responses to changes of seawater carbon chemistry but led to a decrease of net photosynthetic rate when thalli were exposed to increased light intensity. This decrease could be attributed to photodamage caused by the combination of the saved energy due to the down-regulated CCMs and high light intensity. Our findings suggest future ocean acidification might impose depressing effects on green tide events when combined with increased light exposure.

  4. Accelerating Net Terrestrial Carbon Uptake During the Warming Hiatus Due to Reduced Respiration

    Science.gov (United States)

    Ballantyne, Ashley; Smith, William; Anderegg, William; Kauppi, Pekka; Sarmiento, Jorge; Tans, Pieter; Shevliakova, Elena; Pan, Yude; Poulter, Benjamin; Anav, Alessandro; hide

    2017-01-01

    The recent warming hiatus presents an excellent opportunity to investigate climate sensitivity of carbon cycle processes. Here we combine satellite and atmospheric observations to show that the rate of net biome productivity (NBP) has significantly accelerated from - 0.007 +/- 0.065 PgC yr(exp -2) over the warming period (1982 to 1998) to 0.119 +/- 0.071 PgC yr(exp -2) over the warming hiatus (19982012). This acceleration in NBP is not due to increased primary productivity, but rather reduced respiration that is correlated (r = 0.58; P = 0.0007) and sensitive ( y = 4.05 to 9.40 PgC yr(exp -1) per C) to land temperatures. Global land models do not fully capture this apparent reduced respiration over the warming hiatus; however, an empirical model including soil temperature and moisture observations better captures the reduced respiration.

  5. Millennial-scale changes in atmospheric CO2 levels linked to the Southern Ocean carbon isotope gradient and dust flux

    Science.gov (United States)

    Ziegler, Martin; Diz, Paula; Hall, Ian R.; Zahn, Rainer

    2013-06-01

    The rise in atmospheric CO2 concentrations observed at the end of glacial periods has, at least in part, been attributed to the upwelling of carbon-rich deep water in the Southern Ocean. The magnitude of outgassing of dissolved CO2, however, is influenced by the biological fixation of upwelled inorganic carbon and its transfer back to the deep sea as organic carbon. The efficiency of this biological pump is controlled by the extent of nutrient utilization, which can be stimulated by the delivery of iron by atmospheric dust particles. Changes in nutrient utilization should be reflected in the δ13C gradient between intermediate and deep waters. Here we use the δ13C values of intermediate- and bottom-dwelling foraminifera to reconstruct the carbon isotope gradient between thermocline and abyssal water in the subantarctic zone of the South Atlantic Ocean over the past 360,000 years. We find millennial-scale oscillations of the carbon isotope gradient that correspond to changes in dust flux and atmospheric CO2 concentrations as reported from Antarctic ice cores. We interpret this correlation as a relationship between the efficiency of the biological pump and fertilization by dust-borne iron. As the correlation is exponential, we suggest that the sensitivity of the biological pump to dust-borne iron fertilization may be increased when the background dust flux is low.

  6. Responses of calcification of massive and encrusting corals to past, present, and near-future ocean carbon dioxide concentrations

    International Nuclear Information System (INIS)

    Iguchi, Akira; Kumagai, Naoki H.; Nakamura, Takashi; Suzuki, Atsushi; Sakai, Kazuhiko; Nojiri, Yukihiro

    2014-01-01

    Highlights: • Growth rates of two corals in the acidified seawater were evaluated. • Highest growth rates were observed in pre-industrial pCO 2 level. • The growth rates also decreased in the near-future ocean acidification level. • The growth responses were affected by variations of parameters of carbon chemistry. • Bayesian modeling approach was effective for the inference of the best model. - Abstract: In this study, we report the acidification impact mimicking the pre-industrial, the present, and near-future oceans on calcification of two coral species (Porites australiensis, Isopora palifera) by using precise pCO 2 control system which can produce acidified seawater under stable pCO 2 values with low variations. In the analyses, we performed Bayesian modeling approaches incorporating the variations of pCO 2 and compared the results between our modeling approach and classical statistical one. The results showed highest calcification rates in pre-industrial pCO 2 level and gradual decreases of calcification in the near-future ocean acidification level, which suggests that ongoing and near-future ocean acidification would negatively impact coral calcification. In addition, it was expected that the variations of parameters of carbon chemistry may affect the inference of the best model on calcification responses to these parameters between Bayesian modeling approach and classical statistical one even under stable pCO 2 values with low variations

  7. Constraining the climate and ocean pH of the early Earth with a geological carbon cycle model

    Science.gov (United States)

    Krissansen-Totton, Joshua; Arney, Giada N.; Catling, David C.

    2018-04-01

    The early Earth’s environment is controversial. Climatic estimates range from hot to glacial, and inferred marine pH spans strongly alkaline to acidic. Better understanding of early climate and ocean chemistry would improve our knowledge of the origin of life and its coevolution with the environment. Here, we use a geological carbon cycle model with ocean chemistry to calculate self-consistent histories of climate and ocean pH. Our carbon cycle model includes an empirically justified temperature and pH dependence of seafloor weathering, allowing the relative importance of continental and seafloor weathering to be evaluated. We find that the Archean climate was likely temperate (0–50 °C) due to the combined negative feedbacks of continental and seafloor weathering. Ocean pH evolves monotonically from 6.6‑0.4+0.6 (2σ) at 4.0 Ga to 7.0‑0.5+0.7 (2σ) at the Archean–Proterozoic boundary, and to 7.9‑0.2+0.1 (2σ) at the Proterozoic–Phanerozoic boundary. This evolution is driven by the secular decline of pCO2, which in turn is a consequence of increasing solar luminosity, but is moderated by carbonate alkalinity delivered from continental and seafloor weathering. Archean seafloor weathering may have been a comparable carbon sink to continental weathering, but is less dominant than previously assumed, and would not have induced global glaciation. We show how these conclusions are robust to a wide range of scenarios for continental growth, internal heat flow evolution and outgassing history, greenhouse gas abundances, and changes in the biotic enhancement of weathering.

  8. Constraining the climate and ocean pH of the early Earth with a geological carbon cycle model.

    Science.gov (United States)

    Krissansen-Totton, Joshua; Arney, Giada N; Catling, David C

    2018-04-17

    The early Earth's environment is controversial. Climatic estimates range from hot to glacial, and inferred marine pH spans strongly alkaline to acidic. Better understanding of early climate and ocean chemistry