Achieving Negative CO2 Emissions by Protecting Ocean Chemistry

Science.gov (United States)

Cannara, A.

2016-12-01

Industrial Age CO2 added 1.8 trillion tons to the atmosphere. About ¼ has dissolved in seas. The rest still dissolves, bolstered by present emissions of >30 gigatons/year. Airborne & oceanic CO2 have induced sea warming & ocean acidification*. This paper suggests a way to induce a negative CO2-emissions environment for climate & oceans - preserve the planet`s dominant CO2-sequestration system ( 1 gigaton/year via calcifying sea life**) by promptly protecting ocean chemistry via expansion of clean power for both lime production & replacement of CO2-emitting sources. Provide natural alkali (CaO, MgO…) to oceans to maintain average pH above 8.0, as indicated by marine biologists. That alkali (lime) is available from past calcifying life's limestone deposits, so can be returned safely to seas once its CO2 is removed & permanently sequestered (Carbfix, BSCP, etc.***). Limestone is a dense source of CO2 - efficient processing per mole sequestered. Distribution of enough lime is possible via cargo-ship transits - 10,000 tons lime/transit, 1 million transits/year. New Panamax ships carry 120,000 tons. Just 10,000/transit allows gradual reduction of present & past CO2 emissions effects, if coupled with combustion-power reductions. CO2 separation from limestone, as in cement plants, consumes 400kWHrs of thermal energy per ton of output lime (or CO2). To combat yearly CO2 dissolution in seas, we must produce & distribute about 10gigatons of lime/year. Only nuclear power produces the clean energy (thousands of terawatt hours) to meet this need - 1000 dedicated 1GWe reactors, processing 12 cubic miles of limestone/year & sequestering CO2 into a similar mass of basalt. Basalt is common in the world. Researchers*** report it provides good, mineralized CO2 sequestration. The numbers above allow gradual CO2 reduction in air and seas, if we return to President Kennedy's energy path: http://tinyurl.com/6xgpkfa We're on an environmental precipice due to failure to eliminate

The Abundance of Atmospheric CO{sub 2} in Ocean Exoplanets: a Novel CO{sub 2} Deposition Mechanism

Energy Technology Data Exchange (ETDEWEB)

Levi, A.; Sasselov, D. [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States); Podolak, M., E-mail: amitlevi.planetphys@gmail.com [Dept. of Geosciences, Tel Aviv University, Tel Aviv, 69978 (Israel)

2017-03-20

We consider super-Earth sized planets which have a water mass fraction large enough to form an external mantle composed of high-pressure water-ice polymorphs and also lack a substantial H/He atmosphere. We consider such planets in their habitable zone, so that their outermost condensed mantle is a global, deep, liquid ocean. For these ocean planets, we investigate potential internal reservoirs of CO{sub 2}, the amount of CO{sub 2} dissolved in the ocean for the various saturation conditions encountered, and the ocean-atmosphere exchange flux of CO{sub 2}. We find that, in a steady state, the abundance of CO{sub 2} in the atmosphere has two possible states. When wind-driven circulation is the dominant CO{sub 2} exchange mechanism, an atmosphere of tens of bars of CO{sub 2} results, where the exact value depends on the subtropical ocean surface temperature and the deep ocean temperature. When sea-ice formation, acting on these planets as a CO{sub 2} deposition mechanism, is the dominant exchange mechanism, an atmosphere of a few bars of CO{sub 2} is established. The exact value depends on the subpolar surface temperature. Our results suggest the possibility of a negative feedback mechanism, unique to water planets, where a reduction in the subpolar temperature drives more CO{sub 2} into the atmosphere to increase the greenhouse effect.

Characteristics of coupled atmosphere-ocean CO2 sensitivity experiments with different ocean formulations

International Nuclear Information System (INIS)

Washington, W.M.; Meehl, G.A.

1990-01-01

The Community Climate Model at the National Center for Atmospheric Research has been coupled to a simple mixed-layer ocean model and to a coarse-grid ocean general circulation model (OGCM). This paper compares the responses of simulated climate to increases of atmospheric carbon dioxide (CO 2 ) in these two coupled models. Three types of simulations were run: (1) control runs with both ocean models, with CO 2 held constant at present-day concentrations, (2) instantaneous doubling of atmospheric CO 2 (from 330 to 660 ppm) with both ocean models, and (3) a gradually increasing (transient) CO 2 concentration starting at 330 ppm and increasing linearly at 1% per year, with the OGCM. The mixed-layer and OGCM cases exhibit increases of 3.5 C and 1.6 C, respectively, in globally averaged surface air temperature for the instantaneous doubling cases. The transient-forcing case warms 0.7 C by the end of 30 years. The mixed-layer ocean yields warmer-than-observed tropical temperatures and colder-than-observed temperatures in the higher latitudes. The coarse-grid OGCM simulates lower-than-observed sea surface temperatures (SSTs) in the tropics and higher-than-observed SSTs and reduced sea-ice extent at higher latitudes. Sensitivity in the OGCM after 30 years is much lower than in simulations with the same atmosphere coupled to a 50-m slab-ocean mixed layer. The OGCM simulates a weaker thermohaline circulation with doubled CO 2 as the high-latitude ocean-surface layer warms and freshens and the westerly wind stress decreases. Convective overturning in the OGCM decreases substantially with CO 2 warming

Characteristics of coupled atmosphere-ocean CO2 sensitivity experiments with different ocean formulations

International Nuclear Information System (INIS)

Washington, W.M.; Meehl, G.A.

1991-01-01

The Community Climate Model at the National Center for Atmospheric Research has been coupled to a simple mixed-layer ocean model and to a coarse-grid ocean general circulation model (OGCM). This paper compares the responses of simulated climate to increases of atmospheric carbon dioxide (CO 2 ) in these two coupled models. Three types of simulations were run: (1) control runs with both ocean models, with CO 2 held constant at present-day concentrations, (2) instantaneous doubling of atmospheric CO 2 (from 330 to 660 ppm) with both ocean models, and (3) a gradually increasing (transient) CO 2 concentration starting at 330 ppm and increasing linearly at 1% per year, with the OGCM. The mixed-layer and OGCM cases exhibit increases of 3.5 C and 1.6 C, respectively, in globally averaged surface air temperature for the instantaneous doubling cases. The transient-forcing case warms 0.7 C by the end of 30 years. The mixed-layer ocean yields warmer-than-observed tropical temperatures and colder-than-observed temperatures in the higher latitudes. The coarse-grid OGCM simulates lower-than-observed sea surface temperatures (SSTs) in the tropics and higher-than-observed SSTs and reduced sea-ice extent at higher latitudes. Sensitivity in the OGCM after 30 years is much lower than in simulations with the same atmosphere coupled to a 50-m slab-ocean mixed layer. The OGCM simulates a weaker thermohaline circulation with doubled CO 2 as the high-latitude ocean-surface layer warms and freshens and the westerly wind stress decreases. Convective overturning in the OGCM decreases substantially with CO 2 warming. 46 refs.; 20 figs.; 1 tab

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.

Evasion of CO2 injected into the ocean in the context of CO2 stabilization

International Nuclear Information System (INIS)

Kheshgi, Haroon S.

2004-01-01

The eventual evasion of injected CO 2 to the atmosphere is one consideration when assessing deep-sea disposal of CO 2 as a potential response option to climate change concerns. Evasion estimated using an ocean carbon cycle model is compared to long-term trajectories for future CO 2 emissions, including illustrative cases leading to stabilization of CO 2 concentration at various levels. Modeled residence time for CO 2 injected into the deep ocean exceeds the 100-year time-scale usually considered in scenarios for future emissions, and the potential impacts of climate change. Illustrative cases leading monotonically to constant CO 2 concentration have been highlighted by the Intergovernmental Panel on Climate Change to give guidance on possible timing of emission reductions that may be required to stabilize greenhouse gas concentrations at various levels. For stabilization cases considered, significant modeled evasion does not occur until long after CO 2 emissions have reached a maximum and begun to decline. Illustrative cases can also lead to a maximum in CO 2 concentration followed by a decline to slowly decreasing concentrations. In such cases, future injection of emissions into the deep ocean leads to lower maximum CO 2 concentration, with less effect on concentration later on in time

Environmental Assessment for Potential Impacts of Ocean CO2 Storage on Marine Biogeochemical Cycles

Science.gov (United States)

Yamada, N.; Tsurushima, N.; Suzumura, M.; Shibamoto, Y.; Harada, K.

2008-12-01

Ocean CO2 storage that actively utilizes the ocean potential to dissolve extremely large amounts of CO2 is a useful option with the intent of diminishing atmospheric CO2 concentration. CO2 storage into sub-seabed geological formations is also considered as the option which has been already put to practical reconnaissance in some projects. Direct release of CO2 in the ocean storage and potential CO2 leakage from geological formations into the bottom water can alter carbonate system as well as pH of seawater. It is essential to examine to what direction and extent chemistry change of seawater induced by CO2 can affect the marine environments. Previous studies have shown direct and acute effects by increasing CO2 concentrations on physiology of marine organisms. It is also a serious concern that chemistry change can affect the rates of chemical, biochemical and microbial processes in seawater resulting in significant influences on marine biogeochemical cycles of the bioelements including carbon, nutrients and trace metals. We, AIST, have conducted a series of basic researches to assess the potential impacts of ocean CO2 storage on marine biogeochemical processes including CaCO3 dissolution, and bacterial and enzymatic decomposition of organic matter. By laboratory experiments using a special high pressure apparatus, the improved empirical equation was obtained for CaCO3 dissolution rate in the high CO2 concentrations. Based on the experimentally obtained kinetics with a numerical simulation for a practical scenario of oceanic CO2 sequestration where 50 Mton CO2 per year is continuously injected to 1,000-2,500 m depth within 100 x 333 km area for 30 years, we could illustrate precise 3-D maps for the predicted distributions of the saturation depth of CaCO3, in situ Ω value and CaCO3 dissolution rate in the western North Pacific. The result showed no significant change in the bathypelagic CaCO3 flux due to chemistry change induced by ocean CO2 sequestration. Both

A multi-decade record of high-quality fCO2 data in version 3 of the Surface Ocean CO2 Atlas (SOCAT)

Science.gov (United States)

Bakker, Dorothee; Landa, Camilla S.; Pfeil, Benjamin; Metzl, Nicolas; O’Brien, Kevin; Olsen, Are; Smith, Karl; Cosca, Cathy; Harasawa, Sumiko; Nakaoka, Shin-ichiro; Jones, Stephen; Nojiri, Yukihiro; Steinhoff, Tobias; Sweeney, Colm; Schuster, Ute; Takahashi, Taro; Tilbrook, Bronte; Wada, Chisato; Wanninkhof, Rik; Alin, Simone R.; Balestrini, Carlos F.; Barbero, Leticia; Bates, Nicholas; Bianchi, Alejandro A.; Bonou, Frédéric; Boutin, Jacqueline; Bozec, Yann; Burger, Eugene F.; Cai, Wei-Jun; Castle, Robert D.; Chen, Liqi; Chierici, Melissa; Currie, Kim; Evans, Wiley; Featherstone, Charles; Feely, Richard; Fransson, Agneta; Goyet, Catherine; Greenwood, Naomi; Gregor, Luke; Hankin, Steven C.; Hardman-Mountford, Nick J.; Harlay, Jérôme; Hauck, Judith; Hoppema, Mario; Humphreys, Matthew P.; Hunt, Christopher W.; Huss, Betty; Ibánhez, J. Severino P.; Johannessen, Truls; Keeling, Ralph F.; Kitidis, Vassilis; Körtzinger, Arne; Kozyr, Alex; Krasakopoulou, Evangelia; Kuwata, Akira; Landschützer, Peter; Lauvset, Siv K.; Lefèvre, Nathalie; Lo Monaco, Claire; Manke, Ansley; Mathis, Jeremy T.; Merlivat, Liliane; Millero, Frank J.; Monteiro, Pedro M. S.; Munro, David R.; Murata, Akihiko; Newberger, Timothy; Omar, Abdirahman M.; Ono, Tsuneo; Paterson, Kristina; Pearce, David; Pierrot, Denis; Robbins, Lisa L.; Saito, Shu; Salisbury, Joe; Schlitzer, Reiner; Schneider, Bernd; Schweitzer, Roland; Sieger, Rainer; Skjelvan, Ingunn; Sullivan, Kevin F.; Sutherland, Stewart C.; Sutton, Adrienne J.; Tadokoro, Kazuaki; Telszewski, Maciej; Tuma, Matthias; van Heuven, Steven M. A. C.; Vandemark, Douglas; Ward, Brian; Watson, Andrew J.; Xu, Suqing

2016-01-01

The Surface Ocean CO2 Atlas (SOCAT) is a synthesis of quality-controlled f CO2 (fugacity of carbon dioxide) values for the global surface oceans and coastal seas with regular updates. Version 3 of SOCAT has 14.7 million f CO2 values from 3646 data sets covering the years 1957 to 2014. This latest version has an additional 4.6 million f CO2 values relative to version 2 and extends the record from 2011 to 2014. Version 3 also significantly increases the data availability for 2005 to 2013. SOCAT has an average of approximately 1.2 million surface water f CO2 values per year for the years 2006 to 2012. Quality and documentation of the data has improved. A new feature is the data set quality control (QC) flag of E for data from alternative sensors and platforms. The accuracy of surface water f CO2 has been defined for all data set QC flags. Automated range checking has been carried out for all data sets during their upload into SOCAT. The upgrade of the interactive Data Set Viewer (previously known as the Cruise Data Viewer) allows better interrogation of the SOCAT data collection and rapid creation of high-quality figures for scientific presentations. Automated data upload has been launched for version 4 and will enable more frequent SOCAT releases in the future. High-profile scientific applications of SOCAT include quantification of the ocean sink for atmospheric carbon dioxide and its long-term variation, detection of ocean acidification, as well as evaluation of coupled-climate and ocean-only biogeochemical models. Users of SOCAT data products are urged to acknowledge the contribution of data providers, as stated in the SOCAT Fair Data Use Statement. This ESSD (Earth System Science Data) “living data” publication documents the methods and data sets used for the assembly of this new version of the SOCAT data collection and compares these with those used for earlier versions of the data collection (Pfeil et al., 2013; Sabine et al., 2013; Bakker et al., 2014). 

Characteristics of Atmosphere-Ocean CO2 Exchange due to Typhoon Activities over the East Asian Region

Science.gov (United States)

Lee, G.; Cho, C. H.; Lim, D. H.; Sun, M.; Lee, J.; Byun, Y. H.; Lee, J.

2014-12-01

Although the oceans are generally known as a net carbon sink in global sense, it is expected that CO₂release from oceans can occur locally depending on specific weather. This study addresses investigation of change in CO2 exchange between atmosphere and ocean due to typhoon activities, using "Carbon Tracker-Asia (CTA)". The CTA has constructed and managed at National Institute of Meteorological Research(NIMR) based on Carbon Tracker developed by NOAA. In order to examine effect of typhoon on change in air-sea CO2 exchange, we selected several cases which typhoon approached to Korean peninsula in the summertime and their tracks are similar to each other. Also, we analyzed difference between CO2 flux along typhoon tracks and other adjacent region not to be directly affected by typhoon in these cases. There is a difference in ocean fluxes around 15 gC/m²yr over strong typhoon areas compared to other areas. This difference varied with the wind speeds, the correlation coefficient between the ocean and the wind flux was found 0.7. Changes in carbon flux to affect the concentration of CO₂ in the atmosphere near surface instantly.

Isotopic versus micrometeorologic ocean CO2 fluxes: A serious conflict

International Nuclear Information System (INIS)

Broecker, W.S.; Ledwell, J.R.; Takahashi, T.; Weiss, R.; Merlivat, L.; Memery, L.; Tsung-Hung Peng; Jahne, B.; Otto Munnich, K.

1986-01-01

Eddy correlation measurements over the ocean give CO 2 fluxes an order of magnitude or more larger than expected from mass balance or more larger than expected from mass balance measurements using radiocarbon and radon 222. In particular, Smith and Jones (1985) reported large upward and downward fluxes in a surf zone at supersaturations of 15% and attributed them to the equilibration of bubbles at elevated pressures. They argue that even on the open ocean such bubble injection may create steady state CO 2 supersaturations and that inferences of fluxes based on air-sea pCO 2 differences and radon exchange velocities must be made with caution. We defend the global average CO 2 exchange rate determined by three independent radioisotopic means: prebomb radiocarbon inventories; global surveys of mixed layer radon deficits; and oceanic uptake of bomb-produced radiocarbon. We argue that laboratory and lake data do not lead one to expect fluxes as large as reported from the eddy correlation technique; that the radon method of determining exchange velocities is indeed useful for estimating CO 2 fluxes; that supersaturations of CO 2 due to bubble injection on the open ocean are negligible; that the hypothesis that Smith and Jones advance cannot account for the fluxes that they report; and that the pCO 2 values reported by Smith and Jones are likely to be systematically much too high. The CO 2 fluxes for the ocean measured to data by the micrometeorological method can be reconciled with neither the observed concentrations of radioisotopes of radon and carbon in the oceans nor the tracer experiments carried out in lakes and in wind/wave tunnels

Future ocean hypercapnia driven by anthropogenic amplification of the natural CO2 cycle

Science.gov (United States)

McNeil, Ben I.; Sasse, Tristan P.

2016-01-01

High carbon dioxide (CO2) concentrations in sea-water (ocean hypercapnia) can induce neurological, physiological and behavioural deficiencies in marine animals. Prediction of the onset and evolution of hypercapnia in the ocean requires a good understanding of annual variations in oceanic CO2 concentration, but there is a lack of relevant global observational data. Here we identify global ocean patterns of monthly variability in carbon concentration using observations that allow us to examine the evolution of surface-ocean CO2 levels over the entire annual cycle under increasing atmospheric CO2 concentrations. We predict that the present-day amplitude of the natural oscillations in oceanic CO2 concentration will be amplified by up to tenfold in some regions by 2100, if atmospheric CO2 concentrations continue to rise throughout this century (according to the RCP8.5 scenario of the Intergovernmental Panel on Climate Change). The findings from our data are broadly consistent with projections from Earth system climate models. Our predicted amplification of the annual CO2 cycle displays distinct global patterns that may expose major fisheries in the Southern, Pacific and North Atlantic oceans to hypercapnia many decades earlier than is expected from average atmospheric CO2 concentrations. We suggest that these ocean ‘CO2 hotspots’ evolve as a combination of the strong seasonal dynamics of CO2 concentration and the long-term effective storage of anthropogenic CO2 in the oceans that lowers the buffer capacity in these regions, causing a nonlinear amplification of CO2 concentration over the annual cycle. The onset of ocean hypercapnia (when the partial pressure of CO2 in sea-water exceeds 1,000 micro-atmospheres) is forecast for atmospheric CO2 concentrations that exceed 650 parts per million, with hypercapnia expected in up to half the surface ocean by 2100, assuming a high-emissions scenario (RCP8.5). Such extensive ocean hypercapnia has detrimental implications for

Southern Ocean CO2 sink: the contribution of the sea ice

DEFF Research Database (Denmark)

Delille, B.; Vancoppenolle, Martin; Geilfus, Nicolas-Xavier

2014-01-01

at the air-sea ice interface. The sea ice changes from a transient source to a sink for atmospheric CO2. We upscale these observations to the whole Antarctic sea ice cover using the NEMO-LIM3 large-scale sea ice-ocean and provide first esti- mates of spring and summer CO2 uptake from the atmosphere...... by Antarctic sea ice. Over the spring- summer period, the Antarctic sea ice cover is a net sink of atmospheric CO2 of 0.029 Pg C, about 58% of the estimated annual uptake from the Southern Ocean. Sea ice then contributes significantly to the sink of CO2 of the Southern Ocean....... undersaturation while the underlying oceanic waters remains slightly oversaturated. The decrease from winter to summer of pCO2 in the brines is driven by dilution with melting ice, dissolution of carbonate crystals, and net primary production. As the ice warms, its permeability increases, allowing CO2 transfer...

Simulated effect of calcification feedback on atmospheric CO2 and ocean acidification

Science.gov (United States)

Zhang, Han; Cao, Long

2016-01-01

Ocean uptake of anthropogenic CO2 reduces pH and saturation state of calcium carbonate materials of seawater, which could reduce the calcification rate of some marine organisms, triggering a negative feedback on the growth of atmospheric CO2. We quantify the effect of this CO2-calcification feedback by conducting a series of Earth system model simulations that incorporate different parameterization schemes describing the dependence of calcification rate on saturation state of CaCO3. In a scenario with SRES A2 CO2 emission until 2100 and zero emission afterwards, by year 3500, in the simulation without CO2-calcification feedback, model projects an accumulated ocean CO2 uptake of 1462 PgC, atmospheric CO2 of 612 ppm, and surface pH of 7.9. Inclusion of CO2-calcification feedback increases ocean CO2 uptake by 9 to 285 PgC, reduces atmospheric CO2 by 4 to 70 ppm, and mitigates the reduction in surface pH by 0.003 to 0.06, depending on the form of parameterization scheme used. It is also found that the effect of CO2-calcification feedback on ocean carbon uptake is comparable and could be much larger than the effect from CO2-induced warming. Our results highlight the potentially important role CO2-calcification feedback plays in ocean carbon cycle and projections of future atmospheric CO2 concentrations. PMID:26838480

Evasion of CO{sub 2} injected into the ocean in the content of CO{sub 2} stabilization

Energy Technology Data Exchange (ETDEWEB)

Kheshgi, H.S. [ExxonMobil Research and Engineering Co., Annandale, NJ (United States)

2004-08-01

The eventual evasion of injected CO{sub 2} to the atmosphere is one consideration when assessing deep-sea disposal of CO{sub 2} as a potential response option to climate change concerns. Evasion estimated using an ocean carbon cycle model is compared to long-term trajectories for future CO{sub 2} emissions, including illustrative cases leading to stabilization of CO{sub 2} concentration at various levels. Modeled residence time for CO{sub 2} injected into the deep ocean exceeds the 100-year time-scale usually considered in scenarios for future emissions, and the potential impacts of climate change. Illustrative cases leading monotonically to constant CO{sub 2} concentration have been highlighted by the Intergovernmental Panel on Climate Change to give guidance on possible timing of emission reductions that may be required to stabilize greenhouse gas concentrations at various levels. For stabilization cases considered, significant modeled evasion does not occur until long after CO{sub 2} emissions have reached a maximum and begun to decline. Illustrative cases can also lead to a maximum in CO{sub 2} concentration followed by a decline to slowly decreasing concentrations. In such cases, future injection of emissions into the deep ocean leads to lower maximum CO{sub 2} concentration, with less effect on concentration later on in time. (author)

Evasion of CO{sub 2} injected into the ocean in the context of CO{sub 2} stabilization

Energy Technology Data Exchange (ETDEWEB)

Kheshgi, Haroon S

2004-08-01

The eventual evasion of injected CO{sub 2} to the atmosphere is one consideration when assessing deep-sea disposal of CO{sub 2} as a potential response option to climate change concerns. Evasion estimated using an ocean carbon cycle model is compared to long-term trajectories for future CO{sub 2} emissions, including illustrative cases leading to stabilization of CO{sub 2} concentration at various levels. Modeled residence time for CO{sub 2} injected into the deep ocean exceeds the 100-year time-scale usually considered in scenarios for future emissions, and the potential impacts of climate change. Illustrative cases leading monotonically to constant CO{sub 2} concentration have been highlighted by the Intergovernmental Panel on Climate Change to give guidance on possible timing of emission reductions that may be required to stabilize greenhouse gas concentrations at various levels. For stabilization cases considered, significant modeled evasion does not occur until long after CO{sub 2} emissions have reached a maximum and begun to decline. Illustrative cases can also lead to a maximum in CO{sub 2} concentration followed by a decline to slowly decreasing concentrations. In such cases, future injection of emissions into the deep ocean leads to lower maximum CO{sub 2} concentration, with less effect on concentration later on in time.

Field demonstration of CO2 leakage detection in potable aquifers with a pulselike CO2-release test.

Science.gov (United States)

Yang, Changbing; Hovorka, Susan D; Delgado-Alonso, Jesus; Mickler, Patrick J; Treviño, Ramón H; Phillips, Straun

2014-12-02

This study presents two field pulselike CO2-release tests to demonstrate CO2 leakage detection in a shallow aquifer by monitoring groundwater pH, alkalinity, and dissolved inorganic carbon (DIC) using the periodic groundwater sampling method and a fiber-optic CO2 sensor for real-time in situ monitoring of dissolved CO2 in groundwater. Measurements of groundwater pH, alkalinity, DIC, and dissolved CO2 clearly deviated from their background values, showing responses to CO2 leakage. Dissolved CO2 observed in the tests was highly sensitive in comparison to groundwater pH, DIC, and alkalinity. Comparison of the pulselike CO2-release tests to other field tests suggests that pulselike CO2-release tests can provide reliable assessment of geochemical parameters indicative of CO2 leakage. Measurements by the fiber-optic CO2 sensor, showing obvious leakage signals, demonstrated the potential of real-time in situ monitoring of dissolved CO2 for leakage detection at a geologic carbon sequestration (GCS) site. Results of a two-dimensional reactive transport model reproduced the geochemical measurements and confirmed that the decrease in groundwater pH and the increases in DIC and dissolved CO2 observed in the pulselike CO2-release tests were caused by dissolution of CO2 whereas alkalinity was likely affected by carbonate dissolution.

Sugarcane vinasse CO2 gasification and release of ash-forming matters in CO2 and N2 atmospheres.

Science.gov (United States)

Dirbeba, Meheretu Jaleta; Brink, Anders; DeMartini, Nikolai; Lindberg, Daniel; Hupa, Mikko

2016-10-01

Gasification of sugarcane vinasse in CO2 and the release of ash-forming matters in CO2 and N2 atmospheres were investigated using a differential scanning calorimetry and thermogravimetric analyzer (DSC-TGA) at temperatures between 600 and 800°C. The results showed that pyrolysis is the main mechanism for the release of the organics from vinasse. Release of ash-forming matters in the vinasse is the main cause for vinasse char weight losses in the TGA above 700°C. The losses are higher in N2 than in CO2, and increase considerably with temperature. CO2 gasification also consumes the carbon in the vinasse chars while suppressing alkali release. Alkali release was also significant due to volatilization of KCl and reduction of alkali sulfate and carbonate by carbon. The DSC measured thermal events during heating up in N2 atmosphere that correspond to predicted melting temperatures of alkali salts in the char. Copyright © 2016 Elsevier Ltd. All rights reserved.

Atmospheric 14C changes resulting from fossil fuel CO2 release and cosmic ray flux variability

International Nuclear Information System (INIS)

Stuiver, M.; Quay, P.D.

1981-01-01

A high-precision tree-ring record of the atmospheric 14 C levels between 1820 and 1954 is presented. Good agreement is obtained between measured and model calculated 19th and 20th century atmospheric δ 14 C levels when both fossil fuel CO 2 release and predicted natural variations in 14 C production are taken into account. The best fit is obtained by using a box-diffusion model with an oceanic eddy diffusion coefficient of 3 cm 2 /s, a CO 2 atmosphere-ocean gas exchange rate of 21 moles msup(-2) yrsup(-1) and biospheric residence time of 60 years. For trees in the state of Washington the measured 1949-1951 atmospheric δ 14 C level was 20.0 +- 1.2per mille below the 1855-1864 level. Model calculations indicate that in 1950 industrial CO 2 emissions are responsible for at least 85% of the δ 14 C decline, whereas natural variability accounts for the remaining 15%. (orig.)

Evasion of CO{sub 2} injected into the ocean in the context of CO{sub 2} stabilization

Energy Technology Data Exchange (ETDEWEB)

Haroon S. Kheshgi [ExxonMobil Research and Engineering Company, Annandale, NJ (United States)

2003-07-01

The eventual evasion of injected CO{sub 2} to the atmosphere is one consideration when assessing deep sea disposal of CO{sub 2} as a potential response option to climate change concerns. Evasion estimated using an ocean carbon cycle model is compared to long-term trajectories for future CO{sub 2} emissions, including illustrative cases leading to stabilization of CO{sub 2} concentration at various levels. Modeled residence time for CO{sub 2} injected into the deep ocean exceeds the 100-year time scale usually considered in scenarios for future emissions, and the potential impacts of climate change. Illustrative cases leading monotonically to constant CO{sub 2} concentration have been highlighted by the Intergovernmental Panel on Climate Change to give guidance on possible timing of emission reductions that may be required to stabilize greenhouse gas concentrations at various levels. For stabilization cases considered, significant modeled evasion does not occur until long after CO{sub 2} emissions have reached a maximum and begun to decline. Illustrative cases can also lead to a maximum in CO{sub 2} concentration followed by a decline to slowly decreasing concentrations. In such cases, future injection of emissions into the deep ocean leads to lower maximum CO{sub 2} concentration, with less effect on concentration later on in time. 20 refs., 4 figs.

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.

Surface Ocean CO₂ Atlas (SOCAT) gridded data products

Digital Repository Service at National Institute of Oceanography (India)

Sabine, C.L.; Hankin, S.; Koyuk, H.; Bakker, D.C.E.; Pfeil, B.; Olsen, A; Metzl, N.; Kozyr, A; Fassbender, A; Manke, A; Malczyk, J.; Akl, J.; Alin, S.R.; Bellerby, R.G.J.; Borges, A; Boutin, J.; Brown, P.J.; Cai, W.-J.; Chavez, F.P.; Chen, A.; Cosca, C.; Feely, R.A.; Gonzalez-Davila, M.; Goyet, C.; Hardman-Mountford, N.; Heinze, C.; Hoppema, M.; Hunt, C.W.; Hydes, D.; Ishii, M.; Johannessen, T.; Key, R.M.; Kortzinger, A.; Landschutzer, P.; Lauvset, S.K.; Lefevre, N.; Lenton, A.; Lourantou, A.; Merlivat, L.; Midorikawa, T.; Mintrop, L.; Miyazaki, C.; Murata, A.; Nakadate, A.; Nakano, Y.; Nakaoka, S.; Nojiri, Y.; Omar, A.M.; Padin, X.A.; Park, G.-H.; Paterson, K.; Perez, F.F.; Pierrot, D.; Poisson, A.; Rios, A.F.; Salisbury, J.; Santana-Casiano, J.M.; Sarma, V.V.S.S.; et al.

As a response to public demand for a well-documented, quality controlled, publically available, global surface ocean carbon dioxide (CO₂) data set, the international marine carbon science community developed the Surface Ocean CO_2...

Impact of climate change and variability on the global oceanic sink of CO2

OpenAIRE

Le Quéré, Corinne; Takahashi, Taro; Buitenhuis, Erik T.; Rödenbeck, Christian; Sutherland, Stewart C.

2010-01-01

About one quarter of the CO2 emitted to the atmosphere by human activities is absorbed annually by the ocean. All the processes that influence the oceanic uptake of CO2 are controlled by climate. Hence changes in climate (both natural and human-induced) are expected to alter the uptake of CO2 by the ocean. However, available information that constrains the direction, magnitude, or rapidity of the response of ocean CO2 to changes in climate is limited. We present an analysis of oceanic CO2 tre...

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.

Seasonal and mesoscale variability of oceanic transport of anthropogenic CO2

Directory of Open Access Journals (Sweden)

J.-C. Dutay

2009-11-01

Full Text Available Estimates of the ocean's large-scale transport of anthropogenic CO2 are based on one-time hydrographic sections, but the temporal variability of this transport has not been investigated. The aim of this study is to evaluate how the seasonal and mesoscale variability affect data-based estimates of anthropogenic CO2 transport. To diagnose this variability, we made a global anthropogenic CO2 simulation using an eddy-permitting version of the coupled ocean sea-ice model ORCA-LIM. As for heat transport, the seasonally varying transport of anthropogenic CO2 is largest within 20° of the equator and shows secondary maxima in the subtropics. Ekman transport generally drives most of the seasonal variability, but the contribution of the vertical shear becomes important near the equator and in the Southern Ocean. Mesoscale variabilty contributes to the annual-mean transport of both heat and anthropogenic CO2 with strong poleward transport in the Southern Ocean and equatorward transport in the tropics. This "rectified" eddy transport is largely baroclinic in the tropics and barotropic in the Southern Ocean due to a larger contribution from standing eddies. Our analysis revealed that most previous hydrographic estimates of meridional transport of anthropogenic CO2 are severely biased because they neglect temporal fluctuations due to non-Ekman velocity variations. In each of the three major ocean basins, this bias is largest near the equator and in the high southern latitudes. In the subtropical North Atlantic, where most of the hydrographic-based estimates have been focused, this uncertainty represents up to 20% and 30% of total meridional transport of heat and CO2. Generally though, outside the tropics and Southern Ocean, there are only small variations in meridional transport due to seasonal variations in tracer fields and time variations in eddy transport. For the North Atlantic, eddy variability accounts for up to 10% and 15% of the total transport of

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

Investigating the Impact of Past and Future CO2 Emissions on the Distribution of Radiocarbon in the Ocean

Science.gov (United States)

Khatiwala, S.; Payne, S.; Graven, H. D.; Heimbach, P.

2015-12-01

The ocean is a significant sink for carbon dioxide from fossil fuel burning, absorbing roughly a third of human CO2 emitted over the industrial period. This has implications not only for climate but also for the chemical and isotopic composition of the ocean. Human activities have increased the ocean radiocarbon content through nuclear bomb tests in the 1950s-60s, which released a large amount of radiocarbon (14C) into the atmosphere, but fossil fuel emissions are decreasing the radiocarbon content through the release of 14C-depleted CO2. Here, we use the ECCO-v4 ocean state estimate to examine the changing nature of the air-sea flux of radiocarbon and its spatial distribution in the ocean in response to past and future CO2 emissions, the latter taken from the the Representative Concentration Pathway (RCP) database used in IPCC simulations. In line with previous studies we find that the large air-sea gradient of 14C induced by nuclear bomb testing led to rapid accumulation of radiocarbon in the surface ocean. Surface fluxes of 14C have considerably weakened over the past several decades and in some areas 14C is being returned to the atmosphere. As fossil fuel emissions continue to reduce the atmospheric 14C/C ratio (Δ14C), in most RCP scenarios the total ocean 14C inventory starts decreasing by 2030. With strong emissions, the Δ14C of surface waters is driven to increasingly negative values and in RCP 8.5 by 2100 much of the surface ocean has apparent radiocarbon ages in excess of 2000 years, with subtropical gyres more depleted in 14C than the Southern Ocean. Surface waters become significantly more negative in Δ14C than underlying waters. As a result, turning conventional tracer oceanography on its head, recently ventilated waters are characterized by more negative Δ14C values. Similar patterns can be expected for CFCs in the ocean as atmospheric concentrations decrease over the next several decades. Our results have a number of implications, notably for

Surface CO2 leakage during the first shallow subsurface CO2 release experiment

OpenAIRE

Lewicki, J.L.; Oldenburg, C.; Dobeck, L.; Spangler, L.

2008-01-01

A new field facility was used to study CO2 migration processes and test techniques to detect and quantify potential CO2 leakage from geologic storage sites. For 10 days starting 9 July 2007, and for seven days starting 5 August 2007, 0.1 and 0.3 t CO2 d-1, respectively, were released from a ~;100-m long, sub-water table (~;2.5-m depth) horizontal well. The spatio-temporal evolution of leakage was mapped through repeated grid measurements of soil CO2 flux (FCO2). The surface leakage onset...

Characteristics of CO2 release from forest soil in the mountains near Beijing.

Science.gov (United States)

Sun, Xiang Yang; Gao, Cheng Da; Zhang, Lin; Li, Su Yan; Qiao, Yong

2011-04-01

CO2 release from forest soil is a key driver of carbon cycling between the soil and atmosphere ecosystem. The rate of CO2 released from soil was measured in three forest stands (in the mountainous region near Beijing, China) by the alkaline absorption method from 2004 to 2006. The rate of CO2 released did not differ among the three stands. The CO2 release rate ranged from - 341 to 1,193 mg m(-2) h(-1), and the mean value over all three forests and sampling times was 286 mg m(-2) h(-1). CO2 release was positively correlated with soil water content and the soil temperature. Diurnally, CO2 release was higher in the day than at night. Seasonally, CO2 release was highest in early autumn and lowest in winter; in winter, negative values of CO2 release suggested that CO2 was absorbed by soil.

Two decades of ocean CO2 sink and variability

International Nuclear Information System (INIS)

Quere, C. Le; Bopp, L.; Heimann, M.; Prentice, I.C.; Aumont, O.; Bousquet, P.; Ciais, P.; Francey, R.; Rayner, P.J.; Keeling, C.D.; Keeling, R.F.; Piper, S.C.; Kheshgi, H.; Peyliln, P.

2003-01-01

Atmospheric CO 2 has increased at a nearly identical average rate of 3.3 and 3.2 Pg C/yr for the decades of the 1980s and the 1990s, in spite of a large increase in fossil fuel emissions from 5.4 to 6.3 Pg C/yr. Thus, the sum of the ocean and land CO 2 sinks was 1 Pg C/yr larger in the 1990s than in to the 1980s. Here we quantify the ocean and land sinks for these two decades using recent atmospheric inversions and ocean models. The ocean and land sinks are estimated to be, respectively, 0.3 (0.1 to 0.6) and 0.7 (0.4 to 0.9) Pg C/yr larger in the 1990s than in the 1980s. When variability less than 5 yr is removed, all estimates show a global oceanic sink more or less steadily increasing with time, and a large anomaly in the land sink during 1990-1994. For year-to-year variability, all estimates show 1/3 to 1/2 less variability in the ocean than on land, but the amplitude and phase of the oceanic variability remain poorly determined. A mean oceanic sink of 1.9 Pg C/yr for the 1990s based on O 2 observations corrected for ocean outgassing is supported by these estimates, but an uncertainty on the mean value of the order of ±0.7 Pg C/yr remains. The difference between the two decades appears to be more robust than the absolute value of either of the two decades

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.)

Use of hydrate for sequestering CO{sub 2} in the deep ocean

Energy Technology Data Exchange (ETDEWEB)

North, W.J.; Morgan, J.J. [California Inst. of Technology, Pasadena, CA (United States); Spencer, D.F. [Electric Power Research Inst., Palo Alto, CA (United States)] [and others

1993-12-31

Tremendous amounts of CO{sub 2} are accumulating annually in the atmosphere (ca 3 gigatons of carbon per year at present). Prevention or significant amelioration of this atmospheric buildup will obviously require a grand scale corrective activity. A potential solution to the problem might involve sequestering CO{sub 2} in an alternate reservoir. The ocean immediately comes to mind as a reservoir of appropriate magnitude to accommodate the huge quantities of CO{sub 2} involved. Presumably there would be a trade-off: we would achieve a semi-clean atmosphere for an as- yet-to-be-determined impact in the ocean. Minimizing any oceanic impacts would enhance attractiveness of the trade-off.

A hybrid numerical model system of LCO2 and CO2 enriched seawater dynamics in the ocean induced by moving-ship releasing

International Nuclear Information System (INIS)

Chen, B.; Song, Y.; Ohsumi, T.; AIST, Ibaraki; Nishio, M.; Akai, M.

2004-01-01

A numerical modeling system has been developed, based on an engineering background, of the direct disposal of liquid carbon dioxide into the ocean by a moving-ship, to predict the physico-chemical dynamics of liquid carbon dioxide droplets and carbon dioxide enriched seawater in the ocean. This is a hybrid simulation model system consisting of a three-dimensional small-scale near-field model and a two-dimensional horizontal turbulent dispersion model. The dynamics near to release sites include double-plume creation, interaction, evolution, and coupling with ocean currents; these are described by using two-fluid large-eddy simulation technology. The further development of carbon dioxide enriched seawater, as a passive-inert scalar, in relatively larger spatial and time scales (28x28 km and up to 100 h) is then simulated by a horizontal turbulent dispersion model. For the case of liquid carbon dioxide release at a depth of 2000 m with mass flow rate of 100 kg/s and initial droplet diameter of 8.0 mm, and with ship speed of 3.0 m/s, the model predicts a vertically separated carbon dioxide enriched seawater plume, 330 m in height and 40 m in width at time about 1 h after release with a minimum pH of 6.20 corresponding to carbon dioxide concentration of 0.18 kg/m 3 , in the surrounding area. This carbon dioxide enriched seawater plume diffused turbulently in the horizontal surface to an area of 9.8x10.5 km 2 after 100 h. (author)

Pleistocene atmospheric CO2 change linked to Southern Ocean nutrient utilization

Science.gov (United States)

Ziegler, M.; Diz, P.; Hall, I. R.; Zahn, R.

2011-12-01

Biological uptake of CO2 by the ocean and its subsequent storage in the abyss is intimately linked with the global carbon cycle and constitutes a significant climatic force1. The Southern Ocean is a particularly important region because its wind-driven upwelling regime brings CO2 laden abyssal waters to the surface that exchange CO2 with the atmosphere. The Subantarctic Zone (SAZ) is a CO2 sink and also drives global primary productivity as unutilized nutrients, advected with surface waters from the south, are exported via Subantarctic Mode Water (SAMW) as preformed nutrients to the low latitudes where they fuel the biological pump in upwelling areas. Recent model estimates suggest that up to 40 ppm of the total 100 ppm atmospheric pCO2 reduction during the last ice age were driven by increased nutrient utilization in the SAZ and associated feedbacks on the deep ocean alkalinity. Micro-nutrient fertilization by iron (Fe), contained in the airborne dust flux to the SAZ, is considered to be the prime factor that stimulated this elevated photosynthetic activity thus enhancing nutrient utilization. We present a millennial-scale record of the vertical stable carbon isotope gradient between subsurface and deep water (Δδ13C) in the SAZ spanning the past 350,000 years. The Δδ13C gradient, derived from planktonic and benthic foraminifera, reflects the efficiency of biological pump and is highly correlated (rxy = -0.67 with 95% confidence interval [0.63; 0.71], n=874) with the record of dust flux preserved in Antarctic ice cores6. This strongly suggests that nutrient utilization in the SAZ was dynamically coupled to dust-induced Fe fertilization across both glacial-interglacial and faster millennial timescales. In concert with ventilation changes of the deep Southern Ocean this drove ocean-atmosphere CO2 exchange and, ultimately, atmospheric pCO2 variability during the late Pleistocene.

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

Transient modeling of electrochemically assisted CO2 capture and release

DEFF Research Database (Denmark)

Singh, Shobhana; Stechel, Ellen B.; Buttry, Daniel A.

2017-01-01

to analyze the time-dependent behavior of CO2 capture and electro-migration transport across the cell length. Given high nonlinearity of the system, we used a finite element method (FEM) to numerically solve the coupled mass transport equations. The model describes the concentration profiles by taking......The present work aims to develop a model of a new electrochemical CO2 separation and release technology. We present a one-dimensional transient model of an electrochemical cell for point source CO2 capture and release, which mainly focuses on the simultaneous mass transport and complex chemical...... reactions associated with the separation process. For concreteness, we use an ionic liquid (IL) with 2 M thiolate anion (RS−) in 1 M disulfide (RSSR) as an electrolyte in the electrochemical cell to capture, transport and release CO2 under standard operating conditions. We computationally solved the model...

Changing noise levels in a high CO2/lower pH ocean

Science.gov (United States)

Brewer, P. G.; Hester, K. C.; Peltzer, E. T.; Kirkwood, W. J.

2008-12-01

We show that ocean acidification from fossil fuel CO2 invasion and from increased respiration/reduced ventilation, has significantly reduced ocean sound absorption and thus increased ocean noise levels in the kHz frequency range. Below 10 kHz, sound absorption occurs due to well known chemical relaxations in the B(OH)3/B(OH)4- and HCO3-/CO32- systems. The pH dependence of these chemical relaxations results in decreased sound absorption (α = dB/km) as the ocean becomes more acidic from increased CO2 levels. The scale of surface ocean pH change today from the +105 ppmv change in atmospheric CO2 is about - 0.12 pH, resulting in frequency dependent decreases in sound absorption that now exceed 12% over pre- industrial. Under reasonable projections of future fossil fuel CO2 emissions and other sources a pH change of 0.3 units or more can be anticipated by mid-century, resulting in a decrease in α by almost 40%. Increases in water temperature have a smaller effect but also contribute to decreased sound absorption. Combining a lowering of 0.3 pH units with an increase of 3°C, α will decrease further to almost 45%. Ambient noise levels in the ocean within the auditory range critical for environmental, military, and economic interests are set to increase significantly due to the combined effects of decreased absorption and increasing sources from mankind's activities. Incorporation of sound absorption in modeling future ocean scenarios (R. Zeebe, personal communication) and long-term monitoring possibly with the aid of modern cabled observatories can give insights in how ocean noise will continue to change and its effect on groups such as marine mammals which communicate in the affected frequency range.

Fast Atmosphere-Ocean Model Runs with Large Changes in CO2

Science.gov (United States)

Russell, Gary L.; Lacis, Andrew A.; Rind, David H.; Colose, Christopher; Opstbaum, Roger F.

2013-01-01

How does climate sensitivity vary with the magnitude of climate forcing? This question was investigated with the use of a modified coupled atmosphere-ocean model, whose stability was improved so that the model would accommodate large radiative forcings yet be fast enough to reach rapid equilibrium. Experiments were performed in which atmospheric CO2 was multiplied by powers of 2, from 1/64 to 256 times the 1950 value. From 8 to 32 times, the 1950 CO2, climate sensitivity for doubling CO2 reaches 8 C due to increases in water vapor absorption and cloud top height and to reductions in low level cloud cover. As CO2 amount increases further, sensitivity drops as cloud cover and planetary albedo stabilize. No water vapor-induced runaway greenhouse caused by increased CO2 was found for the range of CO2 examined. With CO2 at or below 1/8 of the 1950 value, runaway sea ice does occur as the planet cascades to a snowball Earth climate with fully ice covered oceans and global mean surface temperatures near 30 C.

Temperature dependence of CO2-enhanced primary production in the European Arctic Ocean

KAUST Repository

Holding, J. M.

2015-08-31

The Arctic Ocean is warming at two to three times the global rate1 and is perceived to be a bellwether for ocean acidification2, 3. Increased CO2 concentrations are expected to have a fertilization effect on marine autotrophs4, and higher temperatures should lead to increased rates of planktonic primary production5. Yet, simultaneous assessment of warming and increased CO2 on primary production in the Arctic has not been conducted. Here we test the expectation that CO2-enhanced gross primary production (GPP) may be temperature dependent, using data from several oceanographic cruises and experiments from both spring and summer in the European sector of the Arctic Ocean. Results confirm that CO2 enhances GPP (by a factor of up to ten) over a range of 145–2,099 μatm; however, the greatest effects are observed only at lower temperatures and are constrained by nutrient and light availability to the spring period. The temperature dependence of CO2-enhanced primary production has significant implications for metabolic balance in a warmer, CO2-enriched Arctic Ocean in the future. In particular, it indicates that a twofold increase in primary production during the spring is likely in the Arctic.

Physiological advantages of dwarfing in surviving extinctions in high-CO2 oceans

Science.gov (United States)

Garilli, Vittorio; Rodolfo-Metalpa, Riccardo; Scuderi, Danilo; Brusca, Lorenzo; Parrinello, Daniela; Rastrick, Samuel P. S.; Foggo, Andy; Twitchett, Richard J.; Hall-Spencer, Jason M.; Milazzo, Marco

2015-07-01

Excessive CO2 in the present-day ocean-atmosphere system is causing ocean acidification, and is likely to cause a severe biodiversity decline in the future, mirroring effects in many past mass extinctions. Fossil records demonstrate that organisms surviving such events were often smaller than those before, a phenomenon called the Lilliput effect. Here, we show that two gastropod species adapted to acidified seawater at shallow-water CO2 seeps were smaller than those found in normal pH conditions and had higher mass-specific energy consumption but significantly lower whole-animal metabolic energy demand. These physiological changes allowed the animals to maintain calcification and to partially repair shell dissolution. These observations of the long-term chronic effects of increased CO2 levels forewarn of changes we can expect in marine ecosystems as CO2 emissions continue to rise unchecked, and support the hypothesis that ocean acidification contributed to past extinction events. The ability to adapt through dwarfing can confer physiological advantages as the rate of CO2 emissions continues to increase.

The non-steady state oceanic CO2 signal: its importance, magnitude and a novel way to detect it

Directory of Open Access Journals (Sweden)

B. I. McNeil

2013-04-01

Full Text Available The role of the ocean has been pivotal in modulating rising atmospheric CO2 levels since the industrial revolution, sequestering nearly half of all fossil-fuel derived CO2 emissions. Net oceanic uptake of CO2 has roughly doubled between the 1960s (~1 Pg C yr−1 and 2000s (~2 Pg C yr−1, with expectations that it will continue to absorb even more CO2 with rising future atmospheric CO2 levels. However, recent CO2 observational analyses along with numerous model predictions suggest the rate of oceanic CO2 uptake is already slowing, largely as a result of a natural decadal-scale outgassing signal. This recent CO2 outgassing signal represents a significant shift in our understanding of the oceans role in modulating atmospheric CO2. Current tracer-based estimates for the ocean storage of anthropogenic CO2 assume the ocean circulation and biology is in steady state, thereby missing the new and potentially important "non-steady state" CO2 outgassing signal. By combining data-based techniques that assume the ocean is in a steady state, with techniques that constrain the net oceanic CO2 uptake signal, we show how to extract the non-steady state CO2 signal from observations. Over the entire industrial era, the non-steady state CO2 outgassing signal (~13 ± 10 Pg C is estimated to represent about 9% of the total net CO2 inventory change (~142 Pg C. However, between 1989 and 2007, the non-steady state CO2 outgassing signal (~6.3 Pg C has likely increased to be ~18% of net oceanic CO2 storage over that period (~36 Pg C. The present uncertainty of our data-based techniques for oceanic CO2 uptake limit our capacity to quantify the non-steady state CO2 signal, however with more data and better certainty estimates across a range of diverse methods, this important and growing CO2 signal could be better constrained in the future.

Impact of CO{sub 2} hydrates on ocean carbon dioxide deposition options

Energy Technology Data Exchange (ETDEWEB)

Lund, P C

1995-04-01

The objective of the research project described in this report was to contribute to the research on greenhouse gases and the global environment. The focus is on the concept of storing large amounts of CO{sub 2} in the ocean. The project was divided into three subtasks: (1) a comprehensive study of the thermodynamic, physical and chemical properties of the seawater/CO{sub 2}/hydrate system, (2) establishment of a micro-scale kinetic model for CO{sub 2} hydrate formation and stability, based on (1), and (3) establishment of macro-scale models for various ocean deposition options based on (2). A database of selected thermodynamic functions has been set up. A large database of oceanic data has also been made; for any given coordinates at sea a computer program provides the temperature, salinity and oxygen profiles from the sea surface to the sea floor. The kinetic model predicts the formation and pseudo-stability of a very thin hydrate film which acts as an inhibitor for diffusion of CO{sub 2} into the sea water. The model predicts that the hydrate film reduces the overall flux from a liquid CO{sub 2} source with about 90%. Thermodynamically, pure CO{sub 2} in contact with water might form hydrates at depths below about 400 m, which would indicate that hydrate formation could play a role for all ocean CO{sub 2} deposition options. However, this study shows that other mechanisms significantly reduce the role of hydrate formation. It is finally concluded that although more modelling and experimental work is required within this field of research, the hydrate film may play an important role for all options except from shallow water injection. 86 refs., 32 figs., 16 tabs.

Numerical modeling of pore-scale phenomena during CO2 sequestration in oceanic sediments

International Nuclear Information System (INIS)

Kang, Qinjun; Tsimpanogiannis, Ioannis N.; Zhang, Dongxiao; Lichtner, Peter C.

2005-01-01

Direct disposal of liquid CO 2 on the ocean floor is one of the approaches considered for sequestering CO 2 in order to reduce its concentration in the atmosphere. At oceanic depths deeper than approximately 3000 m, liquid CO 2 density is higher than the density of seawater and CO 2 is expected to sink and form a pool at the ocean floor. In addition to chemical reactions between CO 2 and seawater to form hydrate, fluid displacement is also expected to occur within the ocean floor sediments. In this work, we consider two different numerical models for hydrate formation at the pore scale. The first model consists of the Lattice Boltzmann (LB) method applied to a single-phase supersaturated solution in a constructed porous medium. The second model is based on the Invasion Percolation (IP) in pore networks, applied to two-phase immiscible displacement of seawater by liquid CO 2 . The pore-scale results are upscaled to obtain constitutive relations for porosity, both transverse and for the entire domain, and for permeability. We examine deposition and displacement patterns, and changes in porosity and permeability due to hydrate formation, and how these properties depend on various parameters including a parametric study of the effect of hydrate formation kinetics. According to the simulations, the depth of CO 2 invasion in the sediments is controlled by changes in the pore-scale porosity close to the hydrate formation front. (author)

Quantifying the drivers of ocean-atmosphere CO2 fluxes

Science.gov (United States)

Lauderdale, Jonathan M.; Dutkiewicz, Stephanie; Williams, Richard G.; Follows, Michael J.

2016-07-01

A mechanistic framework for quantitatively mapping the regional drivers of air-sea CO2 fluxes at a global scale is developed. The framework evaluates the interplay between (1) surface heat and freshwater fluxes that influence the potential saturated carbon concentration, which depends on changes in sea surface temperature, salinity and alkalinity, (2) a residual, disequilibrium flux influenced by upwelling and entrainment of remineralized carbon- and nutrient-rich waters from the ocean interior, as well as rapid subduction of surface waters, (3) carbon uptake and export by biological activity as both soft tissue and carbonate, and (4) the effect on surface carbon concentrations due to freshwater precipitation or evaporation. In a steady state simulation of a coarse-resolution ocean circulation and biogeochemistry model, the sum of the individually determined components is close to the known total flux of the simulation. The leading order balance, identified in different dynamical regimes, is between the CO2 fluxes driven by surface heat fluxes and a combination of biologically driven carbon uptake and disequilibrium-driven carbon outgassing. The framework is still able to reconstruct simulated fluxes when evaluated using monthly averaged data and takes a form that can be applied consistently in models of different complexity and observations of the ocean. In this way, the framework may reveal differences in the balance of drivers acting across an ensemble of climate model simulations or be applied to an analysis and interpretation of the observed, real-world air-sea flux of CO2.

Quantifying pCO2 in biological ocean acidification experiments: A comparison of four methods.

Science.gov (United States)

Watson, Sue-Ann; Fabricius, Katharina E; Munday, Philip L

2017-01-01

Quantifying the amount of carbon dioxide (CO2) in seawater is an essential component of ocean acidification research; however, equipment for measuring CO2 directly can be costly and involve complex, bulky apparatus. Consequently, other parameters of the carbonate system, such as pH and total alkalinity (AT), are often measured and used to calculate the partial pressure of CO2 (pCO2) in seawater, especially in biological CO2-manipulation studies, including large ecological experiments and those conducted at field sites. Here we compare four methods of pCO2 determination that have been used in biological ocean acidification experiments: 1) Versatile INstrument for the Determination of Total inorganic carbon and titration Alkalinity (VINDTA) measurement of dissolved inorganic carbon (CT) and AT, 2) spectrophotometric measurement of pHT and AT, 3) electrode measurement of pHNBS and AT, and 4) the direct measurement of CO2 using a portable CO2 equilibrator with a non-dispersive infrared (NDIR) gas analyser. In this study, we found these four methods can produce very similar pCO2 estimates, and the three methods often suited to field-based application (spectrophotometric pHT, electrode pHNBS and CO2 equilibrator) produced estimated measurement uncertainties of 3.5-4.6% for pCO2. Importantly, we are not advocating the replacement of established methods to measure seawater carbonate chemistry, particularly for high-accuracy quantification of carbonate parameters in seawater such as open ocean chemistry, for real-time measures of ocean change, nor for the measurement of small changes in seawater pCO2. However, for biological CO2-manipulation experiments measuring differences of over 100 μatm pCO2 among treatments, we find the four methods described here can produce similar results with careful use.

Optimizing Ocean Space: Co-siting Open Ocean Aquaculture

Science.gov (United States)

Cobb, B. L.; Wickliffe, L. C.; Morris, J. A., Jr.

2016-12-01

In January of 2016, NOAA's National Marine Fisheries Service released the Gulf Aquaculture Plan (GAP) to manage the development of environmentally sound and economically sustainable open ocean finfish aquaculture in the Gulf of Mexico (inside the U.S. Exclusive Economic Zone [EEZ]). The GAP provides the first regulatory framework for aquaculture in federal waters with estimated production of 64 million pounds of finfish, and an estimated economic impact of $264 million annually. The Gulf of Mexico is one of the most industrialized ocean basins in the world, with many existing ocean uses including oil and natural gas production, shipping and commerce, commercial fishing operations, and many protected areas to ensure conservation of valuable ecosystem resources and services. NOAA utilized spatial planning procedures and tools identifying suitable sites for establishing aquaculture through exclusion analyses using authoritative federal and state data housed in a centralized geodatabase. Through a highly collaborative, multi-agency effort a mock permitting exercise was conducted to illustrate the regulatory decision-making process for the Gulf. Further decision-making occurred through exploring co-siting opportunities with oil and natural gas platforms. Logistical co-siting was conducted to reduce overall operational costs by looking at distance to major port and commodity tonnage at each port. Importantly, the process of co-siting allows aquaculture to be coupled with other benefits, including the availability of previously established infrastructure and the reduction of environmental impacts.

Spatio-temporal Variability in Surface Ocean pCO2 Inferred from Observations

OpenAIRE

Jones, Steve

2012-01-01

The variability of surface ocean pCO2 is examined on multiple spatial and temporal scales. Temporal autocorrelation analysis is used to examine pCO2 variability over multiple years. Spatial autocorrelation analysis describes pCO2 variability over multiple spatial scales. Spatial autocorrelation lengths range between

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.

Response of ocean acidification to a gradual increase and decrease of atmospheric CO2

International Nuclear Information System (INIS)

Cao, Long; Zhang, Han; Zheng, Meidi; Wang, Shuangjing

2014-01-01

We perform coupled climate–carbon cycle model simulations to examine changes in ocean acidity in response to idealized change of atmospheric CO 2 . Atmospheric CO 2 increases at a rate of 1% per year to four times its pre-industrial level of 280 ppm and then decreases at the same rate to the pre-industrial level. Our simulations show that changes in surface ocean chemistry largely follow changes in atmospheric CO 2 . However, changes in deep ocean chemistry in general lag behind the change in atmospheric CO 2 because of the long time scale associated with the penetration of excess CO 2 into the deep ocean. In our simulations with the effect of climate change, when atmospheric CO 2 reaches four times its pre-industrial level, global mean aragonite saturation horizon (ASH) shoals from the pre-industrial value of 1288 to 143 m. When atmospheric CO 2 returns from the peak value of 1120 ppm to pre-industrial level, ASH is 630 m, which is approximately the value of ASH when atmospheric CO 2 first increases to 719 ppm. At pre-industrial CO 2 9% deep-sea cold-water corals are surrounded by seawater that is undersaturated with aragonite. When atmospheric CO 2 reaches 1120 ppm, 73% cold-water coral locations are surrounded by seawater with aragonite undersaturation, and when atmospheric CO 2 returns to the pre-industrial level, 18% cold-water coral locations are surrounded by seawater with aragonite undersaturation. Our analysis indicates the difficulty for some marine ecosystems to recover to their natural chemical habitats even if atmospheric CO 2 content can be lowered in the future. (paper)

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.

Eddy covariance observations of surface leakage during shallow subsurface CO2 releases

Science.gov (United States)

Lewicki, Jennifer L.; Hilley, George E.; Fischer, Marc L.; Pan, Lehua; Oldenburg, Curtis M.; Dobeck, Laura; Spangler, Lee

2009-06-01

We tested the ability of eddy covariance (EC) to detect, locate, and quantify surface CO2 flux leakage signals within a background ecosystem. For 10 days starting on 9 July 2007, and for 7 days starting on 3 August 2007, 0.1 (Release 1) and 0.3 (Release 2) t CO2 d-1, respectively, were released from a horizontal well ˜100 m in length and ˜2.5 m in depth located in an agricultural field in Bozeman, Montana. An EC station measured net CO2 flux (Fc) from 8 June 2006 to 4 September 2006 (mean and standard deviation = -12.4 and 28.1 g m-2 d-1, respectively) and from 28 May 2007 to 4 September 2007 (mean and standard deviation = -12.0 and 28.1 g m-2 d-1, respectively). The Release 2 leakage signal was visible in the Fc time series, whereas the Release 1 signal was difficult to detect within variability of ecosystem fluxes. To improve detection ability, we calculated residual fluxes (Fcr) by subtracting fluxes corresponding to a model for net ecosystem exchange from Fc. Fcr had reduced variability and lacked the negative bias seen in corresponding Fc distributions. Plotting the upper 90th percentile Fcr versus time enhanced the Release 2 leakage signal. However, values measured during Release 1 fell within the variability assumed to be related to unmodeled natural processes. Fcr measurements and corresponding footprint functions were inverted using a least squares approach to infer the spatial distribution of surface CO2 fluxes during Release 2. When combined with flux source area evaluation, inversion results roughly located the CO2 leak, while resolution was insufficient to quantify leakage rate.

Tropical CO2 seeps reveal the impact of ocean acidification on coral reef invertebrate recruitment.

Science.gov (United States)

Allen, Ro; Foggo, Andrew; Fabricius, Katharina; Balistreri, Annalisa; Hall-Spencer, Jason M

2017-11-30

Rising atmospheric CO 2 concentrations are causing ocean acidification by reducing seawater pH and carbonate saturation levels. Laboratory studies have demonstrated that many larval and juvenile marine invertebrates are vulnerable to these changes in surface ocean chemistry, but challenges remain in predicting effects at community and ecosystem levels. We investigated the effect of ocean acidification on invertebrate recruitment at two coral reef CO 2 seeps in Papua New Guinea. Invertebrate communities differed significantly between 'reference' (median pH7.97, 8.00), 'high CO 2 ' (median pH7.77, 7.79), and 'extreme CO 2 ' (median pH7.32, 7.68) conditions at each reef. There were also significant reductions in calcifying taxa, copepods and amphipods as CO 2 levels increased. The observed shifts in recruitment were comparable to those previously described in the Mediterranean, revealing an ecological mechanism by which shallow coastal systems are affected by near-future levels of ocean acidification. Copyright © 2016 Elsevier Ltd. All rights reserved.

Anthropogenic CO2 distribution in the North Pacific ocean

Energy Technology Data Exchange (ETDEWEB)

Chen, C [National Sun Yat-Sen University, Kaohsiung (Taiwan, Province of China)

1993-06-01

This paper discusses the penetration depth of anthropogenic CO2 in the North Pacific Ocean based on carbonate data in the literature. The carbonate data in the literature were used to supplement the tracer data showing oceanic mixing features for waters formed in the last 140 years. The deepest penetration over 2,000m was found in the northwest North Pacific. On the other hand, the shallowest penetration to less than 400m was found in the eastern equatorial Pacific. Consequently, it was suggested that penetration depth of anthropogenic CO2 has been controlled by such factors as deep water formation in the Northwest Pacific, upwelling in the equatorial Pacific, and vertical mixing in the western boundary areas. It was revealed that these results are in harmony well with results implied from tritium, C-14, and freons distributions. The total inventory of excess carbon in the North Pacific was 14.7[plus minus]4[times]10[sup 15]g around 1980. 48 refs., 10 figs.

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...

Ocean acidification affects fish spawning but not paternity at CO2 seeps.

Science.gov (United States)

Milazzo, Marco; Cattano, Carlo; Alonzo, Suzanne H; Foggo, Andrew; Gristina, Michele; Rodolfo-Metalpa, Riccardo; Sinopoli, Mauro; Spatafora, Davide; Stiver, Kelly A; Hall-Spencer, Jason M

2016-07-27

Fish exhibit impaired sensory function and altered behaviour at levels of ocean acidification expected to occur owing to anthropogenic carbon dioxide emissions during this century. We provide the first evidence of the effects of ocean acidification on reproductive behaviour of fish in the wild. Satellite and sneaker male ocellated wrasse (Symphodus ocellatus) compete to fertilize eggs guarded by dominant nesting males. Key mating behaviours such as dominant male courtship and nest defence did not differ between sites with ambient versus elevated CO2 concentrations. Dominant males did, however, experience significantly lower rates of pair spawning at elevated CO2 levels. Despite the higher risk of sperm competition found at elevated CO2, we also found a trend of lower satellite and sneaker male paternity at elevated CO2 Given the importance of fish for food security and ecosystem stability, this study highlights the need for targeted research into the effects of rising CO2 levels on patterns of reproduction in wild fish. © 2016 The Author(s).

The sequestration switch. Removing industrial CO2 by direct ocean absorption

International Nuclear Information System (INIS)

Ametistova, Lioudmila; Briden, James; Twidell, John

2002-01-01

This review paper considers direct injection of industrial CO 2 emissions into the mid-water oceanic column below 500 m depth. Such a process is a potential candidate for switching atmospheric carbon emissions directly to long term sequestration, thereby relieving the intermediate atmospheric burden. Given sufficient research justification, the argument is that harmful impact in both the Atmosphere and the biologically rich upper marine layer could be reduced. The paper aims to estimate the role that active intervention, through direct ocean CO 2 storage, could play and to outline further research and assessment for the strategy to be a viable option for climate change mitigation. The attractiveness of direct ocean injection lies in its bypassing of the Atmosphere and upper marine region, its relative permanence, its practicability using existing technologies and its quantification. The difficulties relate to the uncertainty of some fundamental scientific issues, such as plume dynamics, lowered pH of the exposed waters and associated ecological impact, the significant energy penalty associated with the necessary engineering plant and the uncertain costs. Moreover, there are considerable uncertainties regarding related international marine law. Development of the process would require acceptance of the evidence for climate change, strict requirements for large industrial consumers of fossil fuel to reduce CO 2 emissions into the Atmosphere and scientific evidence for the overall beneficial impact of ocean sequestration

Literature review of CO sub 2 behavior in the ocean and its fixation methods

Energy Technology Data Exchange (ETDEWEB)

Sakaguchi, I [and others; CRIEPI, Abiko-shi (Japan). Abiko Research Lab.

1991-01-01

CO{sub 2} behaviour in the ocean and its fixation methods are reviewed. Intermediate and deep water is an important carbon reservoir in the ocean. It is estimated that plenty of carbon, 37,700 GtC, is stored in the intermediate and deep water as compared with the storage in the atmosphere and surface water, 725 GtC each. Main carbon transportation routes in the ocean are (1) downward flux by sinking of carbonate particles, organic particles and water from surface, and (2) upward flux by upwelling of dissolved carbon rich deep water. Because 10{sup 3} years are estimated to be required for deep water upwelling to surface, organic and carbonate particles sinking into the intermediate and deep water are considered to be stored for a long term. Biomass of marine algae and its primary production are estimated to be 2-5 GtC and 10-40 GtC/year respectively. Two to five per cent of the primary production is estimated to be transported from surface to more than 1000 m deep as marine snow or fecal pellets. Following three methods are considered to be possible candidates to reduce atmospheric CO{sub 2} using marine organisms: (1) increasing macroalgae biomass to be used as biomass energy; (2) fixing CO{sub 2} as CaCO{sub 3} like coral reefs; (3) adding micronutrients such as iron to ocean surface water for increasing the primary production and the amount of carbon particles sinking to a deep layer. Following subjects should be studied before utilizing these methods in the ocean: (1) cost reduction for biomass production for increasing macroalgae biomass; (2) CO{sub 2} balance during classification for fixing CO{sub 2} as CaCO{sub 3}; (3) cleaning limiting factors for algae production, how to spread micronutrients to vast sea area and assessing possible environmental effects of adding micronutrients.

Temporal and spatial variations of oceanic pCO2 and air-sea CO2 flux in th Greenland Sea and the Barents Sea

International Nuclear Information System (INIS)

Nakaoka, Shin-Ichiro; Aoki, Shuji; Nakazawa, Takakiyo; Yoshikawa-Inoue, Hisayuki

2006-01-01

In order to elucidate the seasonal and inter annual variations of oceanic CO 2 uptake in the Greenland Sea and the Barents Sea, the partial pressure of CO 2 in the surface ocean (pCO 2 sea ) was measured in all seasons between 1992 and 2001. We derived monthly varying relationships between pCO 2 sea and sea surface temperature (SST) and combined them with the SST data from the NCEP/NCAR reanalysis to determine pCO 2 sea and air-sea CO 2 flux in these seas. The pCO 2 sea values were normalized to the year 1995 by assuming that pCO 2 sea increased at the same growth rate (1.5 μatm/yr) of the pCO 2 in the air (pCO 2 air ) between 1992 and 2001. In 1995, the annual net air-sea CO 2 fluxes were evaluated to be 52 ± 20 gC/m 2 /yr in the Greenland Sea and 46 ± 18 gC/m 2 /yr in the Barents Sea. The CO 2 flux into the ocean reached its maximum in winter and minimum in summer. The wind speed and (delta)pCO 2 (=pCO 2 air -pCO 2 sea ) exerted a greater influence on the seasonal variation than the sea ice coverage. The annual CO 2 uptake examined in this study (70-80 deg N, 20 deg W-40 deg E) was estimated to be 0.050 ± 0.020 GtC/yr in 1995. The inter annual variation in the annual CO 2 uptake was found to be positively correlated with the North Atlantic Oscillation Index (NAOI) via wind strength but negatively correlated with (delta)pCO 2 and the sea ice coverage. The present results indicate that the variability in wind speed and sea ice coverage play a major role, while that in (delta)pCO 2 plays a minor role, in determining the interannual variation of CO 2 uptake in this area

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)

Interannual drivers of the seasonal cycle of CO2 in the Southern Ocean

Directory of Open Access Journals (Sweden)

L. Gregor

2018-04-01

Full Text Available Resolving and understanding the drivers of variability of CO2 in the Southern Ocean and its potential climate feedback is one of the major scientific challenges of the ocean-climate community. Here we use a regional approach on empirical estimates of pCO2 to understand the role that seasonal variability has in long-term CO2 changes in the Southern Ocean. Machine learning has become the preferred empirical modelling tool to interpolate time- and location-restricted ship measurements of pCO2. In this study we use an ensemble of three machine-learning products: support vector regression (SVR and random forest regression (RFR from Gregor et al. (2017, and the self-organising-map feed-forward neural network (SOM-FFN method from Landschützer et al. (2016. The interpolated estimates of ΔpCO2 are separated into nine regions in the Southern Ocean defined by basin (Indian, Pacific, and Atlantic and biomes (as defined by Fay and McKinley, 2014a. The regional approach shows that, while there is good agreement in the overall trend of the products, there are periods and regions where the confidence in estimated ΔpCO2 is low due to disagreement between the products. The regional breakdown of the data highlighted the seasonal decoupling of the modes for summer and winter interannual variability. Winter interannual variability had a longer mode of variability compared to summer, which varied on a 4–6-year timescale. We separate the analysis of the ΔpCO2 and its drivers into summer and winter. We find that understanding the variability of ΔpCO2 and its drivers on shorter timescales is critical to resolving the long-term variability of ΔpCO2. Results show that ΔpCO2 is rarely driven by thermodynamics during winter, but rather by mixing and stratification due to the stronger correlation of ΔpCO2 variability with mixed layer depth. Summer pCO2 variability is consistent with chlorophyll a variability, where higher concentrations of chlorophyll

Interannual drivers of the seasonal cycle of CO2 in the Southern Ocean

Science.gov (United States)

Gregor, Luke; Kok, Schalk; Monteiro, Pedro M. S.

2018-04-01

Resolving and understanding the drivers of variability of CO2 in the Southern Ocean and its potential climate feedback is one of the major scientific challenges of the ocean-climate community. Here we use a regional approach on empirical estimates of pCO2 to understand the role that seasonal variability has in long-term CO2 changes in the Southern Ocean. Machine learning has become the preferred empirical modelling tool to interpolate time- and location-restricted ship measurements of pCO2. In this study we use an ensemble of three machine-learning products: support vector regression (SVR) and random forest regression (RFR) from Gregor et al. (2017), and the self-organising-map feed-forward neural network (SOM-FFN) method from Landschützer et al. (2016). The interpolated estimates of ΔpCO2 are separated into nine regions in the Southern Ocean defined by basin (Indian, Pacific, and Atlantic) and biomes (as defined by Fay and McKinley, 2014a). The regional approach shows that, while there is good agreement in the overall trend of the products, there are periods and regions where the confidence in estimated ΔpCO2 is low due to disagreement between the products. The regional breakdown of the data highlighted the seasonal decoupling of the modes for summer and winter interannual variability. Winter interannual variability had a longer mode of variability compared to summer, which varied on a 4-6-year timescale. We separate the analysis of the ΔpCO2 and its drivers into summer and winter. We find that understanding the variability of ΔpCO2 and its drivers on shorter timescales is critical to resolving the long-term variability of ΔpCO2. Results show that ΔpCO2 is rarely driven by thermodynamics during winter, but rather by mixing and stratification due to the stronger correlation of ΔpCO2 variability with mixed layer depth. Summer pCO2 variability is consistent with chlorophyll a variability, where higher concentrations of chlorophyll a correspond with lower pCO2

Biological and physical controls in the Southern Ocean on past millennial-scale atmospheric CO2 changes.

Science.gov (United States)

Gottschalk, Julia; Skinner, Luke C; Lippold, Jörg; Vogel, Hendrik; Frank, Norbert; Jaccard, Samuel L; Waelbroeck, Claire

2016-05-17

Millennial-scale climate changes during the last glacial period and deglaciation were accompanied by rapid changes in atmospheric CO2 that remain unexplained. While the role of the Southern Ocean as a 'control valve' on ocean-atmosphere CO2 exchange has been emphasized, the exact nature of this role, in particular the relative contributions of physical (for example, ocean dynamics and air-sea gas exchange) versus biological processes (for example, export productivity), remains poorly constrained. Here we combine reconstructions of bottom-water [O2], export production and (14)C ventilation ages in the sub-Antarctic Atlantic, and show that atmospheric CO2 pulses during the last glacial- and deglacial periods were consistently accompanied by decreases in the biological export of carbon and increases in deep-ocean ventilation via southern-sourced water masses. These findings demonstrate how the Southern Ocean's 'organic carbon pump' has exerted a tight control on atmospheric CO2, and thus global climate, specifically via a synergy of both physical and biological processes.

Assessment of particle size distribution in CO 2 accidental releases

NARCIS (Netherlands)

Hulsbosch-Dam, C.E.C.; Spruijt, M.P.N.; Necci, A.; Cozzani, V.

2012-01-01

A model was developed to calculate the particle size distribution following the release of pressurised supercritical CO 2. The model combines several sub-models for the different stages of jet break-up and specifically addresses the possible formation of solid particles, which is important for CO 2

Modeling Effects of Bicarbonate Release on Carbonate Chemistry and pH of the North Sea: A Pilot Study for Atmospheric CO2 Reduction

Science.gov (United States)

Lettmann, K.; Kirchner, J.; Schnetger, B.; Wolff, J. O.; Brumsack, H. J.

2016-12-01

Rising CO2-emissions accompanying the industrial revolution are the main drivers for climate change and ocean acidification. Several methods have been developed to capture CO2 from effluents and reduce emission. Here, we consider a promising approach that mimics natural limestone weathering: CO2 in effluent gas streams reacts with calcium carbonate in a limestone suspension. The resulting bicarbonate-rich solution can be released into natural systems. In comparison to classical carbon capture and storage (CCS) methods this artificial limestone weathering is cheaper and does not involve using toxic chemical compounds. Additionally there is no need for the controversially discussed storage of CO2 underground. The reduction of CO2-emissions becomes more important for European industries as the EU introduced a system that limits the amount of allowable CO2-emissions. Therefore, large CO2 emitters are forced to find cheap methods for emission reduction, as they often cannot circumvent CO2-production. The method mentioned above is especially of interest for power plants located close to the coast that are already using seawater for cooling purposes. Thus, it is important to estimate the environmental effects if several coastal power plants will release high amounts of bicarbonate-rich waters into coastal waters, e.g. the North Sea. In a first pilot study, the unstructured-grid finite-volume community ocean model (FVCOM) was combined with a chemical submodul (mocsy 2.0) to model the hydrodynamic circulation and mixing of bicarbonate-rich effluents from a gas power plant located at the German North Sea coast. Here, we present the first preliminary results of this project, which include modelled changes of the North Sea carbonate system and changes in pH value after the introduction of these bicarbonate-rich waters on short time scales up to one year.

Surface Ocean CO2 Atlas Database Version 5 (SOCATv5) (NCEI Accession 0163180)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — The Surface Ocean CO2 Atlas (SOCAT, www.socat.info) is a synthesis activity by the international marine carbon research community and has more than 100 contributors...

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.

The other ocean acidification problem: CO2 as a resource among competitors for ecosystem dominance

Science.gov (United States)

Connell, Sean D.; Kroeker, Kristy J.; Fabricius, Katharina E.; Kline, David I.; Russell, Bayden D.

2013-01-01

Predictions concerning the consequences of the oceanic uptake of increasing atmospheric carbon dioxide (CO2) have been primarily occupied with the effects of ocean acidification on calcifying organisms, particularly those critical to the formation of habitats (e.g. coral reefs) or their maintenance (e.g. grazing echinoderms). This focus overlooks direct and indirect effects of CO2 on non-calcareous taxa that play critical roles in ecosystem shifts (e.g. competitors). We present the model that future atmospheric [CO2] may act as a resource for mat-forming algae, a diverse and widespread group known to reduce the resilience of kelp forests and coral reefs. We test this hypothesis by combining laboratory and field CO2 experiments and data from ‘natural’ volcanic CO2 vents. We show that mats have enhanced productivity in experiments and more expansive covers in situ under projected near-future CO2 conditions both in temperate and tropical conditions. The benefits of CO2 are likely to vary among species of producers, potentially leading to shifts in species dominance in a high CO2 world. We explore how ocean acidification combines with other environmental changes across a number of scales, and raise awareness of CO2 as a resource whose change in availability could have wide-ranging community consequences beyond its direct effects. PMID:23980244

The other ocean acidification problem: CO2 as a resource among competitors for ecosystem dominance.

Science.gov (United States)

Connell, Sean D; Kroeker, Kristy J; Fabricius, Katharina E; Kline, David I; Russell, Bayden D

2013-01-01

Predictions concerning the consequences of the oceanic uptake of increasing atmospheric carbon dioxide (CO2) have been primarily occupied with the effects of ocean acidification on calcifying organisms, particularly those critical to the formation of habitats (e.g. coral reefs) or their maintenance (e.g. grazing echinoderms). This focus overlooks direct and indirect effects of CO2 on non-calcareous taxa that play critical roles in ecosystem shifts (e.g. competitors). We present the model that future atmospheric [CO2] may act as a resource for mat-forming algae, a diverse and widespread group known to reduce the resilience of kelp forests and coral reefs. We test this hypothesis by combining laboratory and field CO2 experiments and data from 'natural' volcanic CO2 vents. We show that mats have enhanced productivity in experiments and more expansive covers in situ under projected near-future CO2 conditions both in temperate and tropical conditions. The benefits of CO2 are likely to vary among species of producers, potentially leading to shifts in species dominance in a high CO2 world. We explore how ocean acidification combines with other environmental changes across a number of scales, and raise awareness of CO2 as a resource whose change in availability could have wide-ranging community consequences beyond its direct effects.

The footprint of CO2 leakage in the water-column: Insights from numerical modeling based on a North Sea gas release experiment

Science.gov (United States)

Vielstädte, L.; Linke, P.; Schmidt, M.; Sommer, S.; Wallmann, K.; McGinnis, D. F.; Haeckel, M.

2013-12-01

Assessing the environmental impact of potential CO2 leakage from offshore carbon dioxide storage sites necessitates the investigation of the corresponding pH change in the water-column. Numerical models have been developed to simulate the buoyant rise and dissolution of CO2 bubbles in the water-column and the subsequent near-field dispersion of dissolved CO2 in seawater under ocean current and tidal forcing. In order to test and improve numerical models a gas release experiment has been conducted at 80 m water-depth within the Sleipner area (North Sea). CO2 and Kr (used as inert tracer gas) were released on top of a benthic lander at varying gas flows (impact of such leakage rates is limited to the near-field bottom waters, due to the rapid dissolution of CO2 bubbles in seawater (CO2 is being stripped within the first two to five meters of bubble rise). In particular, small bubbles, which will dissolve close to the seafloor, may cause a dangerous low-pH environment for the marine benthos. However, on the larger scale, the advective transport by e.g. tidal currents, dominates the CO2 dispersal in the North Sea and dilutes the CO2 peak quickly. The model results show that at the small scales (impact on the marine environment, thereby reducing pH substantially (by 0.4 units) within a diameter of less than 50 m around the release spot (depending on the duration of leakage and the current velocities). Strong currents and tidal cycles significantly reduce the spreading of low-pH water masses into the far-field by efficiently diluting the amount of CO2 in ambient seawater.

Westerly Winds and the Southern Ocean CO2 Sink Since the Last Glacial-Interglacial Transition

Science.gov (United States)

Hodgson, D. A.; Saunders, K. M.; Roberts, S. J.; Perren, B.; Butz, C.; Sime, L. C.; Davies, S. J.; Grosjean, M.

2017-12-01

The capacity of the Southern Ocean carbon sink is partly controlled by the Southern Hemisphere westerly winds (SHW) and sea ice. These regulate the upwelling of dissolved carbon-rich deep water to Antarctic surface waters, determine the surface area for air-sea gas exchange and therefore modulate the net uptake of atmospheric CO2. Some models have proposed that strengthened SHW will result in a weakening of the Southern Ocean CO2 sink. If these models are correct, then one would expect that reconstructions of changes in SHW intensity on centennial to millennial timescales would show clear links with Antarctic ice core and Southern Ocean marine geological records of atmospheric CO2, temperature and sea ice. Here, we present a 12,300 year reconstruction of past wind strength based on three independent proxies that track the changing inputs of sea salt aerosols and minerogenic particles into lake sediments on sub-Antarctic Macquarie Island. The proxies are consistent in showing that periods of high wind intensity corresponded with the increase in CO2 across the late Last Glacial-Interglacial Transition and in the last 7,000 years, suggesting that the winds have contributed to the long term outgassing of CO2 from the ocean during these periods.

MERIS Ocean Colour Data for the Estimation of Surface Water pCO2: The Case Studies of Peru and Namibia

DEFF Research Database (Denmark)

Karagali, Ioanna; Badger, Merete; Sørensen, Lise Lotte

2010-01-01

Carbon dioxide fluxes between the ocean and atmosphere are important when trying to estimate the amount of existing atmospheric CO2. The ocean can potentially be considered as a storage or source of CO2 depending on temperature, salinity, biological activity and wind. To identify the role...... of a region, CO2 fluxes must be estimated. The air-sea exchange of CO2 depends on the partial pressures of atmospheric and oceanic CO2 and a wind related exchange coefficient. Direct in situ measurements are expensive, operationally demanding and of low spatial resolution. It has been shown that indirect...... estimation of oceanic pCO2 is possible due to its strong dependence on temperature. Primary production may also influence the CO2 concentration in the water, due to the consumption by phytoplankton. The present study aims at estimating the oceanic pCO2 with the use of satellite measurements for water...

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...

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

Transport and absorption of CO2 in the ocean

International Nuclear Information System (INIS)

Nydal, Reidar; Gislefoss, Jorunn S.

1999-01-01

The overview gives an account of C 1 4. C 1 3, C 1 2, DIC (dissolved inorganic carbon), CO 2 , salt and plankton concentration and sea temperature during the last 2 decades in the Atlantic Ocean and particularly in the Norwegian Ocean. Atmospheric radioactive carbon concentrations, sea water flow patterns as well as carbon, salt, temperature and plankton depth profiles have been studied. There does not seem to be significant alterations in the C 1 4 concentration in the Norwegian Sea. Measurements from the Scotland - Greenland ridge have not yet been carried out. -Significant rise in DIC concentrations were not found but it is most likely that the alterations will increase during the 21st century. The plankton concentrations showed seasonal variations and decreased with sea depth. Proposals for further investigations are made

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.

Ocean acidification effects on calcification in pCO2 acclimated Caribbean scleractinian coral

Science.gov (United States)

Ocean acidification (OA) is projected to increase the acidity of coral reef habitats 2-3 times that of present day pCO2 levels. Many studies have shown the adverse effects on scleractinian calcification when exposed to elevated pCO2 levels, however, in these studies, corals have ...

Quantifying the influence of CO2 seasonality on future ocean acidification

Science.gov (United States)

Sasse, T. P.; McNeil, B. I.; Matear, R. J.; Lenton, A.

2015-04-01

Ocean acidification is a predictable consequence of rising atmospheric carbon dioxide (CO2), and is highly likely to impact the entire marine ecosystem - from plankton at the base to fish at the top. Factors which are expected to be impacted include reproductive health, organism growth and species composition and distribution. Predicting when critical threshold values will be reached is crucial for projecting the future health of marine ecosystems and for marine resources planning and management. The impacts of ocean acidification will be first felt at the seasonal scale, however our understanding how seasonal variability will influence rates of future ocean acidification remains poorly constrained due to current model and data limitations. To address this issue, we first quantified the seasonal cycle of aragonite saturation state utilizing new data-based estimates of global ocean surface dissolved inorganic carbon and alkalinity. This seasonality was then combined with earth system model projections under different emissions scenarios (RCPs 2.6, 4.5 and 8.5) to provide new insights into future aragonite under-saturation onset. Under a high emissions scenario (RCP 8.5), our results suggest accounting for seasonality will bring forward the initial onset of month-long under-saturation by 17 years compared to annual-mean estimates, with differences extending up to 35 ± 17 years in the North Pacific due to strong regional seasonality. Our results also show large-scale under-saturation once atmospheric CO2 reaches 486 ppm in the North Pacific and 511 ppm in the Southern Ocean independent of emission scenario. Our results suggest that accounting for seasonality is critical to projecting the future impacts of ocean acidification on the marine environment.

CO2-Induced ATP-Dependent Release of Acetylcholine on the Ventral Surface of the Medulla Oblongata.

Science.gov (United States)

Huckstepp, Robert T R; Llaudet, Enrique; Gourine, Alexander V

2016-01-01

Complex mechanisms that detect changes in brainstem parenchymal PCO2/[H+] and trigger adaptive changes in lung ventilation are responsible for central respiratory CO2 chemosensitivity. Previous studies of chemosensory signalling pathways suggest that at the level of the ventral surface of the medulla oblongata (VMS), CO2-induced changes in ventilation are (at least in part) mediated by the release and actions of ATP and/or acetylcholine (ACh). Here we performed simultaneous real-time biosensor recordings of CO2-induced ATP and ACh release from the VMS in vivo and in vitro, to test the hypothesis that central respiratory CO2 chemosensory transduction involves simultaneous recruitment of purinergic and cholinergic signalling pathways. In anaesthetised and artificially ventilated rats, an increase in inspired CO2 triggered ACh release on the VMS with a peak amplitude of ~5 μM. Release of ACh was only detected after the onset of CO2-induced activation of the respiratory activity and was markedly reduced (by ~70%) by ATP receptor blockade. In horizontal slices of the VMS, CO2-induced release of ATP was reliably detected, whereas CO2 or bath application of ATP (100 μM) failed to trigger release of ACh. These results suggest that during hypercapnia locally produced ATP induces or potentiates the release of ACh (likely from the medullary projections of distal groups of cholinergic neurones), which may also contribute to the development and/or maintenance of the ventilatory response to CO2.

Environmental impacts of ocean disposal of CO2. First quarterly report, September 1--September 30, 1994

International Nuclear Information System (INIS)

Tester, J.W.

1994-01-01

This paper is divided into five sections (corresponding to five tasks) which all must be considered in order to determine the ultimate environmental impact of ocean disposal of CO 2 . The sections are: ambient physical and chemical properties of the ocean; CO 2 loadings (i.e. quantities and purities of CO 2 ) produced using different capture technologies; methods of CO 2 transport and injection, and their associated physical/chemical perturbations; environmental impacts for the scenarios outlined in section the previous section; and other considerations including legal issues, public perception, and monitoring requirements

FY 1999 report on the results of the R and D project on the industrial technology for the global environment. R and D of the prediction technology of environmental effects brought by CO2 ocean sequestration (Ocean survey and development of evaluation technology for CO2 sequestration ability); 1999 nendo chikyu kankyo sangyo gijutsu kenkyu kaihatsu jigyo NEDO seika hokokusho. Nisankatanso no kaiyo kakuri ni tomonau kankyo eikyo yosoku gijutsu kenkyu kaihatsu (Kaiyo chosa oyobi CO2 kakuri noryoku hyoka gijutsu no kaihatsu)

Energy Technology Data Exchange (ETDEWEB)

NONE

2000-03-01

Assuming the melting and sequestration of CO2 at the intermediate depth of the sea area around Japan, study of evaluation technology of CO2 sequestration ability in ocean was studied, and the FY 1999 results were summed up. In the ocean survey, survey was conducted by ship (No.2 Hakurei-maru) mainly at typical observation points and traverse lines of long. 147 E and long. 155 E. In the survey, the following data were acquired: data on seawater density and chemical tracer, data on release of intermediate-depth/independent buoys, concentration distribution of carbonic acid base substances/nutrient salts/chlorophyll, data on the existing amount of marine organisms and primary production speed measurement experiment, data on experiment on CO2 on-board exposure to organisms in the intermediate depth of ocean, etc. In the measurement/analysis of the sediment particle flux amount, sediment traps were installed/recovered. Further, for the purpose of measuring the neutralizing effect of calcium carbonate, operation test on CaCO{sub 3} melting experimental equipment was conducted in the actual sea area. In the development of a model for evaluation of CO2 sequestration ability, carried out were the improvement of the model using the inverse method, study of the estimated accuracy using the ocean observation data, etc. (NEDO)

Global high-resolution monthly pCO2 climatology for the coastal ocean derived from neural network interpolation

Directory of Open Access Journals (Sweden)

G. G. Laruelle

2017-10-01

Full Text Available In spite of the recent strong increase in the number of measurements of the partial pressure of CO2 in the surface ocean (pCO2, the air–sea CO2 balance of the continental shelf seas remains poorly quantified. This is a consequence of these regions remaining strongly under-sampled in both time and space and of surface pCO2 exhibiting much higher temporal and spatial variability in these regions compared to the open ocean. Here, we use a modified version of a two-step artificial neural network method (SOM-FFN; Landschützer et al., 2013 to interpolate the pCO2 data along the continental margins with a spatial resolution of 0.25° and with monthly resolution from 1998 to 2015. The most important modifications compared to the original SOM-FFN method are (i the much higher spatial resolution and (ii the inclusion of sea ice and wind speed as predictors of pCO2. The SOM-FFN is first trained with pCO2 measurements extracted from the SOCATv4 database. Then, the validity of our interpolation, in both space and time, is assessed by comparing the generated pCO2 field with independent data extracted from the LDVEO2015 database. The new coastal pCO2 product confirms a previously suggested general meridional trend of the annual mean pCO2 in all the continental shelves with high values in the tropics and dropping to values beneath those of the atmosphere at higher latitudes. The monthly resolution of our data product permits us to reveal significant differences in the seasonality of pCO2 across the ocean basins. The shelves of the western and northern Pacific, as well as the shelves in the temperate northern Atlantic, display particularly pronounced seasonal variations in pCO2,  while the shelves in the southeastern Atlantic and in the southern Pacific reveal a much smaller seasonality. The calculation of temperature normalized pCO2 for several latitudes in different oceanic basins confirms that the seasonality in shelf pCO2 cannot solely be explained by

CO sub(2) and N sub(2) O fluxes from the northern Indian Ocean

Digital Repository Service at National Institute of Oceanography (India)

Narvekar, P.V.; Naqvi, S.W.A.; DileepKumar, M.

and the deep water concentrations signify quantities of N sub(2)O to be consumed within the sediments. The northern Indian Ocean as a source of CO sub(2) to the atmosphere is poorly quantified. The N sub(2)O data indicate that the vertical diffusion coefficient...

Observations of CO{sub 2} clathrate hydrate formation and dissolution under deep-ocean disposal conditions

Energy Technology Data Exchange (ETDEWEB)

Warzinski, R.P.; Cugini, A.V. [Department of Energy, Pittsburgh, PA (United States); Holder, G.D. [Univ. of Pittsburgh, Pittsburgh, PA (United States)

1995-11-01

Disposal of anthropogenic emissions of CO{sub 2} may be required to mitigate rises in atmospheric levels of this greenhouse gas if other measures are ineffective and the worst global warming scenarios begin to occur. Long-term storage of large quantities of CO{sub 2} has been proposed, but the feasibility of large land and ocean disposal options remains to be established. Determining the fate of liquid CO{sub 2} injected into the ocean at depths greater than 500 m is complicated by uncertainties associated with the physical behavior of CO{sub 2} under these conditions, in particular the possible formation of the ice-like CO{sub 2} clathrate hydrate. Resolving this issue is key to establishing the technical feasibility of this option. Experimental and theoretical work in this area is reported.

Possible impacts of CO2 storage on the marine environment

International Nuclear Information System (INIS)

Poremski, H.J.

2005-01-01

This study examined the potential impacts of deep-sea carbon dioxide (CO 2 ) sequestration on the marine environment. The upper layers of oceans are currently saturated with CO 2 , while deeper ocean waters remain undersaturated. Arctic and Antarctic waters have higher uptake rates of CO 2 due to their lower temperatures. CO 2 deposited in Arctic and Antarctic waters sinks to the bottom of the ocean, and is then transported to equatorial latitudes, where stored amounts of CO 2 that are not fixed by biochemical processes will be released and enter the atmosphere again after a period of approximately 1000 years. Nearly 50 per cent of CO 2 fixation occurs as a result of phytoplankton growth, which is dependent on the availability of a range of nutrients, essential trace metals, and optimal physical conditions. Fertilization-induced CO 2 fixation in the sediments of southern oceans will result in nutrient depletion of bottom layers, which will in turn result in lower primary production levels at equatorial latitudes. Current modelling approaches to CO 2 injection assume that the injected CO 2 will dissolve in a plume extending 100 m around a riser. Retention times of several hundred years are anticipated. However, further research is needed to investigate the efficacy of CO 2 deep ocean storage technologies. Increased CO 2 uptake can also increase the formation of bicarbonate (HCO 3 ) acidification, decrease pH values, and inhibit the formation of biomass in addition to impacting on the calcification of many organisms. It was concluded that ocean storage by injection or deep storage is an untenable option at present due to the fact that the effects of excessive CO 2 in marine environments are not fully understood. 22 refs., 2 tabs

The role of Southern Ocean mixing and upwelling in glacial-interglacial atmospheric CO2 change

International Nuclear Information System (INIS)

Watson, Andrew J.; Naveira Garabato, Alberto C.

2006-01-01

Decreased ventilation of the Southern Ocean in glacial time is implicated in most explanations of lower glacial atmospheric CO 2 . Today, the deep (>2000 m) ocean south of the Polar Front is rapidly ventilated from below, with the interaction of deep currents with topography driving high mixing rates well up into the water column. We show from a buoyancy budget that mixing rates are high in all the deep waters of the Southern Ocean. Between the surface and 2000 m depth, water is upwelled by a residual meridional overturning that is directly linked to buoyancy fluxes through the ocean surface. Combined with the rapid deep mixing, this upwelling serves to return deep water to the surface on a short time scale. We propose two new mechanisms by which, in glacial time, the deep Southern Ocean may have been more isolated from the surface. Firstly, the deep ocean appears to have been more stratified because of denser bottom water resulting from intense sea ice formation near Antarctica. The greater stratification would have slowed the deep mixing. Secondly, subzero atmospheric temperatures may have meant that the present-day buoyancy flux from the atmosphere to the ocean surface was reduced or reversed. This in turn would have reduced or eliminated the upwelling (contrary to a common assumption, upwelling is not solely a function of the wind stress but is coupled to the air/sea buoyancy flux too). The observed very close link between Antarctic temperatures and atmospheric CO 2 could then be explained as a natural consequence of the connection between the air/sea buoyancy flux and upwelling in the Southern Ocean, if slower ventilation of the Southern Ocean led to lower atmospheric CO 2 . Here we use a box model, similar to those of previous authors, to show that weaker mixing and reduced upwelling in the Southern Ocean can explain the low glacial atmospheric CO 2 in such a formulation

The millennial atmospheric lifetime of anthropogenic CO2

International Nuclear Information System (INIS)

Archer, D.

2008-01-01

The notion is pervasive in the climate science community and in the public at large that the climate impacts of fossil fuel CO 2 release will only persist for a few centuries. This conclusion has no basis in theory or models of the atmosphere/ocean carbon cycle, which we review here. The largest fraction of the CO 2 recovery will take place on time scales of centuries, as CO 2 invades the ocean, but a significant fraction of the fossil fuel CO 2 , ranging in published models in the literature from 20-60%, remains airborne for a thousand years or longer. Ultimate recovery takes place on time scales of hundreds of thousands of years, a geologic longevity typically associated in public perceptions with nuclear waste. The glacial/interglacial climate cycles demonstrate that ice sheets and sea level respond dramatically to millennial-timescale changes in climate forcing. There are also potential positive feedbacks in the carbon cycle, including methane hydrates in the ocean, and peat frozen in permafrost, that are most sensitive to the long tail of the fossil fuel CO 2 in the atmosphere

Climatological Distributions of pH, pCO2, Total CO2, Alkalinity, and CaCO3 Saturation in the Global Surface Ocean (NCEI accession 01645680) (NCEI Accession 0164568)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Climatological mean monthly distributions of pH in the total H+ scale, total CO2 concentration (TCO2), and the degree of CaCO3 saturation for the global surface...

Model-Based Assessment of the CO2 Sequestration Potential of Coastal Ocean Alkalinization

Science.gov (United States)

Feng, E. Y.; Koeve, W.; Keller, D. P.; Oschlies, A.

2017-12-01

The potential of coastal ocean alkalinization (COA), a carbon dioxide removal (CDR) climate engineering strategy that chemically increases ocean carbon uptake and storage, is investigated with an Earth system model of intermediate complexity. The CDR potential and possible environmental side effects are estimated for various COA deployment scenarios, assuming olivine as the alkalinity source in ice-free coastal waters (about 8.6% of the global ocean's surface area), with dissolution rates being a function of grain size, ambient seawater temperature, and pH. Our results indicate that for a large-enough olivine deployment of small-enough grain sizes (10 µm), atmospheric CO2 could be reduced by more than 800 GtC by the year 2100. However, COA with coarse olivine grains (1000 µm) has little CO2 sequestration potential on this time scale. Ambitious CDR with fine olivine grains would increase coastal aragonite saturation Ω to levels well beyond those that are currently observed. When imposing upper limits for aragonite saturation levels (Ωlim) in the grid boxes subject to COA (Ωlim = 3.4 and 9 chosen as examples), COA still has the potential to reduce atmospheric CO2 by 265 GtC (Ωlim = 3.4) to 790 GtC (Ωlim = 9) and increase ocean carbon storage by 290 Gt (Ωlim = 3.4) to 913 Gt (Ωlim = 9) by year 2100.

Scaling laws for perturbations in the ocean-atmosphere system following large CO2 emissions

Science.gov (United States)

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

2015-07-01

Scaling relationships are found for perturbations to atmosphere and ocean variables from large transient CO2 emissions. Using the Long-term Ocean-atmosphere-Sediment CArbon cycle Reservoir (LOSCAR) model (Zeebe et al., 2009; Zeebe, 2012b), we calculate perturbations to atmosphere temperature, total carbon, ocean temperature, total ocean carbon, pH, alkalinity, marine-sediment carbon, and carbon-13 isotope anomalies in the ocean and atmosphere resulting from idealized CO2 emission events. The peak perturbations in the atmosphere and ocean variables are then fit to power law functions of the form of γ DαEβ, where D is the event duration, E is its total carbon emission, and γ is a coefficient. Good power law fits are obtained for most system variables for E up to 50 000 PgC and D up to 100 kyr. Although all of the peak perturbations increase with emission rate E/D, we find no evidence of emission-rate-only scaling, α + β = 0. Instead, our scaling yields α + β ≃ 1 for total ocean and atmosphere carbon and 0 < α + β < 1 for most of the other system variables.

CO2-induced ocean acidification does not affect individual or group behaviour in a temperate damselfish.

Science.gov (United States)

Kwan, Garfield Tsz; Hamilton, Trevor James; Tresguerres, Martin

2017-07-01

Open ocean surface CO 2 levels are projected to reach approximately 800 µatm, and ocean pH to decrease by approximately 0.3 units by the year 2100 due to anthropogenic CO 2 emissions and the subsequent process of ocean acidification (OA). When exposed to these CO 2 /pH values, several fish species display abnormal behaviour in laboratory tests, an effect proposed to be linked to altered neuronal GABA A- receptor function. Juvenile blacksmith ( Chromis punctipinnis ) are social fish that regularly experience CO 2 /pH fluctuations through kelp forest diurnal primary production and upwelling events, so we hypothesized that they might be resilient to OA. Blacksmiths were exposed to control conditions (pH ∼ 7.92; p CO 2  ∼ 540 µatm), constant acidification (pH ∼ 7.71; p CO 2  ∼ 921 µatm) and oscillating acidification (pH ∼ 7.91, p CO 2  ∼ 560 µatm (day), pH ∼ 7.70, p CO 2  ∼ 955 µatm (night)), and caught and tested in two seasons of the year when the ocean temperature was different: winter (16.5 ± 0.1°C) and summer (23.1 ± 0.1°C). Neither constant nor oscillating CO 2 -induced acidification affected blacksmith individual light/dark preference, inter-individual distance in a shoal or the shoal's response to a novel object, suggesting that blacksmiths are tolerant to projected future OA conditions. However, blacksmiths tested during the winter demonstrated significantly higher dark preference in the individual light/dark preference test, thus confirming season and/or water temperature as relevant factors to consider in behavioural tests.

Pontellid copepods, Labidocera spp., affected by ocean acidification: A field study at natural CO2 seeps.

Science.gov (United States)

Smith, Joy N; Richter, Claudio; Fabricius, Katharina E; Cornils, Astrid

2017-01-01

CO2 seeps in coral reefs were used as natural laboratories to study the impacts of ocean acidification on the pontellid copepod, Labidocera spp. Pontellid abundances were reduced by ∼70% under high-CO2 conditions. Biological parameters and substratum preferences of the copepods were explored to determine the underlying causes of such reduced abundances. Stage- and sex-specific copepod lengths, feeding ability, and egg development were unaffected by ocean acidification, thus changes in these physiological parameters were not the driving factor for reduced abundances under high-CO2 exposure. Labidocera spp. are demersal copepods, hence they live amongst reef substrata during the day and emerge into the water column at night. Deployments of emergence traps showed that their preferred reef substrata at control sites were coral rubble, macro algae, and turf algae. However, under high-CO2 conditions they no longer had an association with any specific substrata. Results from this study indicate that even though the biology of a copepod might be unaffected by high-CO2, Labidocera spp. are highly vulnerable to ocean acidification.

Pontellid copepods, Labidocera spp., affected by ocean acidification: A field study at natural CO2 seeps.

Directory of Open Access Journals (Sweden)

Joy N Smith

Full Text Available CO2 seeps in coral reefs were used as natural laboratories to study the impacts of ocean acidification on the pontellid copepod, Labidocera spp. Pontellid abundances were reduced by ∼70% under high-CO2 conditions. Biological parameters and substratum preferences of the copepods were explored to determine the underlying causes of such reduced abundances. Stage- and sex-specific copepod lengths, feeding ability, and egg development were unaffected by ocean acidification, thus changes in these physiological parameters were not the driving factor for reduced abundances under high-CO2 exposure. Labidocera spp. are demersal copepods, hence they live amongst reef substrata during the day and emerge into the water column at night. Deployments of emergence traps showed that their preferred reef substrata at control sites were coral rubble, macro algae, and turf algae. However, under high-CO2 conditions they no longer had an association with any specific substrata. Results from this study indicate that even though the biology of a copepod might be unaffected by high-CO2, Labidocera spp. are highly vulnerable to ocean acidification.

Ocean acidification: The little-known impact of CO2 emissions

International Nuclear Information System (INIS)

Madsen, Michael Amdi

2015-01-01

Ocean acidification, like global warming, is a serious consequence of rising carbon dioxide (CO 2 ) emissions and a growing threat to coastal communities. Scientists and economists alike are calling for ocean acidification mitigation and adaptation plans to be included in any future international climate change agreement, arguing that doing so would make any such agreement stronger and facilitate its implementation. The IAEA uses nuclear techniques to measure ocean acidification and has been providing objective information to scientists, economists, and policymakers to make informed decisions. “Recognizing that billions of people are dependent on a healthy ocean for their wellbeing and economic development is the first step,” said Alexandre Magnan of the Institute for Sustainable Development and International Relations in Paris at an IAEA workshop this year. Acknowledging in the legal text of a climate deal the threats facing the oceans could open the door for coastal communities affected by ocean acidification to benefit from financing available under a climate change agreement, he said. This would enable them to adapt to changing social and economic circumstances, improve understanding of the ecological and biophysical changes expected, and pressure further concrete actions by governments, he added.

Ocean acidification: The little-known impact of CO_2 emissions

International Nuclear Information System (INIS)

Madsen, Michael Amdi

2015-01-01

Ocean acidification, like global warming, is a serious consequence of rising carbon dioxide (CO_2) emissions and a growing threat to coastal communities. Scientists and economists alike are calling for ocean acidification mitigation and adaptation plans to be included in any future international climate change agreement, arguing that doing so would make any such agreement stronger and facilitate its implementation. The IAEA uses nuclear techniques to measure ocean acidification and has been providing objective information to scientists, economists, and policymakers to make informed decisions. “Recognizing that billions of people are dependent on a healthy ocean for their wellbeing and economic development is the first step,” said Alexandre Magnan of the Institute for Sustainable Development and International Relations in Paris at an IAEA workshop this year. Acknowledging in the legal text of a climate deal the threats facing the oceans could open the door for coastal communities affected by ocean acidification to benefit from financing available under a climate change agreement, he said. This would enable them to adapt to changing social and economic circumstances, improve understanding of the ecological and biophysical changes expected, and pressure further concrete actions by governments, he added.

The seasonal cycle of pCO2 and CO2 fluxes in the Southern Ocean: diagnosing anomalies in CMIP5 Earth system models

Science.gov (United States)

Precious Mongwe, N.; Vichi, Marcello; Monteiro, Pedro M. S.

2018-05-01

The Southern Ocean forms an important component of the Earth system as a major sink of CO2 and heat. Recent studies based on the Coupled Model Intercomparison Project version 5 (CMIP5) Earth system models (ESMs) show that CMIP5 models disagree on the phasing of the seasonal cycle of the CO2 flux (FCO2) and compare poorly with available observation products for the Southern Ocean. Because the seasonal cycle is the dominant mode of CO2 variability in the Southern Ocean, its simulation is a rigorous test for models and their long-term projections. Here we examine the competing roles of temperature and dissolved inorganic carbon (DIC) as drivers of the seasonal cycle of pCO2 in the Southern Ocean to explain the mechanistic basis for the seasonal biases in CMIP5 models. We find that despite significant differences in the spatial characteristics of the mean annual fluxes, the intra-model homogeneity in the seasonal cycle of FCO2 is greater than observational products. FCO2 biases in CMIP5 models can be grouped into two main categories, i.e., group-SST and group-DIC. Group-SST models show an exaggeration of the seasonal rates of change of sea surface temperature (SST) in autumn and spring during the cooling and warming peaks. These higher-than-observed rates of change of SST tip the control of the seasonal cycle of pCO2 and FCO2 towards SST and result in a divergence between the observed and modeled seasonal cycles, particularly in the Sub-Antarctic Zone. While almost all analyzed models (9 out of 10) show these SST-driven biases, 3 out of 10 (namely NorESM1-ME, HadGEM-ES and MPI-ESM, collectively the group-DIC models) compensate for the solubility bias because of their overly exaggerated primary production, such that biologically driven DIC changes mainly regulate the seasonal cycle of FCO2.

International Collaboration on CO2 Sequestration

Energy Technology Data Exchange (ETDEWEB)

Peter H. Israelsson; E. Eric Adams

2007-06-30

On December 4, 1997, the US Department of Energy (USDOE), the New Energy and Industrial Technology Development Organization of Japan (NEDO), and the Norwegian Research Council (NRC) entered into a Project Agreement for International Collaboration on CO{sub 2} Ocean Sequestration. Government organizations from Japan, Canada, and Australia, and a Swiss/Swedish engineering firm later joined the agreement, which outlined a research strategy for ocean carbon sequestration via direct injection. The members agreed to an initial field experiment, with the hope that if the initial experiment was successful, there would be subsequent field evaluations of increasingly larger scale to evaluate environmental impacts of sequestration and the potential for commercialization. The evolution of the collaborative effort, the supporting research, and results for the International Collaboration on CO{sub 2} Ocean Sequestration were documented in almost 100 papers and reports, including 18 peer-reviewed journal articles, 46 papers, 28 reports, and 4 graduate theses. These efforts were summarized in our project report issued January 2005 and covering the period August 23, 1998-October 23, 2004. An accompanying CD contained electronic copies of all the papers and reports. This report focuses on results of a two-year sub-task to update an environmental assessment of acute marine impacts resulting from direct ocean sequestration. The approach is based on the work of Auerbach et al. [6] and Caulfield et al. [20] to assess mortality to zooplankton, but uses updated information concerning bioassays, an updated modeling approach and three modified injection scenarios: a point release of negatively buoyant solid CO{sub 2} hydrate particles from a moving ship; a long, bottom-mounted diffuser discharging buoyant liquid CO{sub 2} droplets; and a stationary point release of hydrate particles forming a sinking plume. Results suggest that in particular the first two discharge modes could be

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)

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)

Mathematical model of CO2 release during milk fermentation using natural kefir grains.

Science.gov (United States)

Goršek, Andreja; Ritonja, Jožef; Pečar, Darja

2018-03-12

Milk fermentation takes place in the presence of various micro-organisms, producing a variety of dairy products. The oldest of them is kefir, which is usually produced by the fermentation of milk with kefir grains. Carbon dioxide (CO 2 ), as one of the process products, also contributes to the characteristic flavor of kefir. The amount of CO 2 generated during fermentation depends on bioprocessing conditions and may change, which is not desirable at the industrial level. In this study we developed a simplified mathematical model of CO 2 release in the milk-fermentation process. An intuitive approach based on superposition and experimental analysis was used for the modeling. The chemical system studied was considered as a two-input (temperature, rotational frequency of the stirrer) one-output (CO 2 concentration) dynamic system. Based on an analysis of CO 2 release transients in the case of non-simultaneous stepwise changed input quantities, two differential equations were defined that describe the influence of the two input quantities on the output quantity. The simulation results were verified by experiments. The proposed model can be used for a comprehensive analysis of the process that is being studied and for the design and synthesis of advanced control systems, which will ensure a controlled CO 2 release at the industrial level. © 2018 Society of Chemical Industry. © 2018 Society of Chemical Industry.

Atmospheric inversion of the surface CO2 flux with 13CO2 constraint

Science.gov (United States)

Chen, J. M.; Mo, G.; Deng, F.

2013-10-01

Observations of 13CO2 at 73 sites compiled in the GLOBALVIEW database are used for an additional constraint in a global atmospheric inversion of the surface CO2 flux using CO2 observations at 210 sites for the 2002-2004 period for 39 land regions and 11 ocean regions. This constraint is implemented using the 13CO2/CO2 flux ratio modeled with a terrestrial ecosystem model and an ocean model. These models simulate 13CO2 discrimination rates of terrestrial photosynthesis and respiration and ocean-atmosphere diffusion processes. In both models, the 13CO2 disequilibrium between fluxes to and from the atmosphere is considered due to the historical change in atmospheric 13CO2 concentration. For the 2002-2004 period, the 13CO2 constraint on the inversion increases the total land carbon sink from 3.40 to 3.70 Pg C yr-1 and decreases the total oceanic carbon sink from 1.48 to 1.12 Pg C yr-1. The largest changes occur in tropical areas: a considerable decrease in the carbon source in the Amazon forest, and this decrease is mostly compensated by increases in the ocean region immediately west of the Amazon and the southeast Asian land region. Our further investigation through different treatments of the 13CO2/CO2 flux ratio used in the inversion suggests that variable spatial distributions of the 13CO2 isotopic discrimination rate simulated by the models over land and ocean have considerable impacts on the spatial distribution of the inverted CO2 flux over land and the inversion results are not sensitive to errors in the estimated disequilibria over land and ocean.

The millennial atmospheric lifetime of anthropogenic CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Archer, D. [University of Chicago, IL (United States). Department of the Geophysical Sciences; Brovkin, V. [Potsdam Institute for Climate Impact Research (Germany)

2008-10-15

The notion is pervasive in the climate science community and in the public at large that the climate impacts of fossil fuel CO{sub 2} release will only persist for a few centuries. This conclusion has no basis in theory or models of the atmosphere/ocean carbon cycle, which we review here. The largest fraction of the CO{sub 2} recovery will take place on time scales of centuries, as CO{sub 2} invades the ocean, but a significant fraction of the fossil fuel CO{sub 2}, ranging in published models in the literature from 20-60%, remains airborne for a thousand years or longer. Ultimate recovery takes place on time scales of hundreds of thousands of years, a geologic longevity typically associated in public perceptions with nuclear waste. The glacial/interglacial climate cycles demonstrate that ice sheets and sea level respond dramatically to millennial-timescale changes in climate forcing. There are also potential positive feedbacks in the carbon cycle, including methane hydrates in the ocean, and peat frozen in permafrost, that are most sensitive to the long tail of the fossil fuel CO{sub 2} in the atmosphere.

FINAL TECHNICAL REPORT-THE ECOLOGY AND GENOMICS OF CO2 FIXATIION IN OCEANIC RIVER PLUMES

Energy Technology Data Exchange (ETDEWEB)

PAUL, JOHN H

2013-06-21

Oceanic river plumes represent some of the most productive environments on Earth. As major conduits for freshwater and nutrients into the coastal ocean, their impact on water column ecosystems extend for up to a thousand km into oligotrophic oceans. Upon entry into the oceans rivers are tremendous sources of CO2 and dissolved inorganic carbon (DIC). Yet owing to increased light transmissivity from sediment deposition coupled with the influx of nutrients, dramatic CO2 drawdown occurs, and plumes rapidly become sinks for CO2. Using state-of-the-art gene expression technology, we have examined the molecular biodiversity of CO2 fixation in the Mississippi River Plume (MRP; two research cruises) and the Orinoco River Plume (ORP; one cruise). When the MRP extends far into the Gulf because of entrainment with the Loop Current, MRP production (carbon fixation) can account for up to 41% of the surface production in the Gulf of Mexico. Nearer-shore plume stations (“high plume,” salinity< 32 ppt) had tremendous CO2 drawdown that was correlated to heterokont (principally diatom) carbon fixation gene expression. The principal form of nitrogen for this production based upon 15N studies was urea, believed to be from anthropogenic origin (fertilizer) from the MRP watershed. Intermediate plume environments (salinity 34 ppt) were characterized by high levels of Synechococcuus carbon fixation that was fueled by regenerated ammonium. Non-plume stations were characterized by high light Prochlorococcus carbon fixation gene expression that was positively correlated with dissolved CO2 concentrations. Although data from the ORP cruise is still being analyzed, some similarities and striking differences were found between the ORP and MRP. High levels of heterokont carbon fixation gene expression that correlated with CO2 drawdown were observed in the high plume, yet the magnitude of this phenomenon was far below that of the MRP, most likely due to the lower levels of anthropogenic

NEOTEC: Negative-CO2-Emissions Marine Energy With Direct Mitigation of Global Warming, Sea-Level Rise and Ocean Acidification

Science.gov (United States)

Rau, G. H.; Baird, J.; Noland, G.

2016-12-01

The vertical thermal energy potential in the ocean is a massive renewable energy resource that is growing due to anthropogenic warming of the surface and near-surface ocean. The conversion of this thermal energy to useful forms via Ocean Thermal Energy Conversion (OTEC) has been demonstrated over the past century, albeit at small scales. Because OTEC removes heat from the surface ocean, this could help directly counter ongoing, deleterious ocean/atmosphere warming. The only other climate intervention that could do this is solar radiation "geoengineering". Conventional OTEC requires energy intensive, vertical movement of seawater resulting in ocean and atmospheric chemistry alteration, but this can be avoided via more energy efficient, vertical closed-cycle heating and cooling of working fluid like CO2 or NH3. An energy carrier such as H2 is required to transport energy optimally extracted far offshore, and methods of electrochemically generating H2 while also consuming CO2 and converting it to ocean alkalinity have been demonstrated. The addition of such alkalinity to the ocean would provide vast, stable, carbon storage, while also helping chemically counter the effects of ocean acidification. The process might currently be profitable given the >$100/tonne CO2 credit offered by California's Low Carbon Fuel Standard for transportation fuels like H2. Negative-Emissions OTEC, NEOTEC, thus can potentially provide constant, cost effective, high capacity, negative-emissions energy while: a) reducing surface ocean heat load, b) reducing thermal ocean expansion and sea-level rise, c) utilizing a very large, natural marine carbon storage reservoir, and d) helping mitigate ocean acidification. The technology also avoids the biophysical and land use limitations posed by negative emissions methods that rely on terrestrial biology, such as afforestation and BECCS. NEOTEC and other marine-based, renewable energy and CO2 removal approaches could therefore greatly increase the

Increased Ocean Heat Convergence Into the High Latitudes With CO ₂ Doubling Enhances Polar-Amplified Warming: OCEAN HEAT AND POLAR WARMING

Energy Technology Data Exchange (ETDEWEB)

Singh, H. A. [Atmospheric Science and Global Change Division, Pacific Northwest National Laboratory, U.S. DOE Office of Science, Richland WA USA; Rasch, P. J. [Atmospheric Science and Global Change Division, Pacific Northwest National Laboratory, U.S. DOE Office of Science, Richland WA USA; Rose, B. E. J. [Department of Atmospheric and Environmental Sciences, State University of New York at Albany, Albany NY USA

2017-10-18

We isolate the role of the ocean in polar climate change by directly evaluating how changes in ocean dynamics with quasi-equilibrium CO2-doubling impact high-latitude climate. With CO2-doubling, the ocean heat flux convergence (OHFC) shifts poleward in winter in both hemispheres. Imposing this pattern of perturbed OHFC in a global climate model results in a poleward shift in ocean-to-atmosphere turbulent heat fluxes (both sensible and latent) and sea ice retreat; the high-latitudes warm while the midlatitudes cool, thereby amplifying polar warming. Furthermore, midlatitude cooling is propagated to the polar mid-troposphere on isentropic surfaces, augmenting the (positive) lapse rate feedback at high latitudes. These results highlight the key role played by the partitioning of meridional energy transport changes between the atmosphere and ocean in high-latitude climate change.

Reduced calcification of marine plankton in response to increased atmospheric CO2.

Science.gov (United States)

Riebesell, U; Zondervan, I; Rost, B; Tortell, P D; Zeebe, R E; Morel, F M

2000-09-21

The formation of calcareous skeletons by marine planktonic organisms and their subsequent sinking to depth generates a continuous rain of calcium carbonate to the deep ocean and underlying sediments. This is important in regulating marine carbon cycling and ocean-atmosphere CO2 exchange. The present rise in atmospheric CO2 levels causes significant changes in surface ocean pH and carbonate chemistry. Such changes have been shown to slow down calcification in corals and coralline macroalgae, but the majority of marine calcification occurs in planktonic organisms. Here we report reduced calcite production at increased CO2 concentrations in monospecific cultures of two dominant marine calcifying phytoplankton species, the coccolithophorids Emiliania huxleyi and Gephyrocapsa oceanica. This was accompanied by an increased proportion of malformed coccoliths and incomplete coccospheres. Diminished calcification led to a reduction in the ratio of calcite precipitation to organic matter production. Similar results were obtained in incubations of natural plankton assemblages from the north Pacific ocean when exposed to experimentally elevated CO2 levels. We suggest that the progressive increase in atmospheric CO2 concentrations may therefore slow down the production of calcium carbonate in the surface ocean. As the process of calcification releases CO2 to the atmosphere, the response observed here could potentially act as a negative feedback on atmospheric CO2 levels.

Natural and industrial analogues for release of CO2 from storagereservoirs: Identification of features, events, and processes and lessonslearned

Energy Technology Data Exchange (ETDEWEB)

Lewicki, Jennifer L.; Birkholzer, Jens; Tsang, Chin-Fu

2006-03-03

The injection and storage of anthropogenic CO{sub 2} in deep geologic formations is a potentially feasible strategy to reduce CO{sub 2} emissions and atmospheric concentrations. While the purpose of geologic carbon storage is to trap CO{sub 2} underground, CO{sub 2} could migrate away from the storage site into the shallow subsurface and atmosphere if permeable pathways such as well bores or faults are present. Large-magnitude releases of CO{sub 2} have occurred naturally from geologic reservoirs in numerous volcanic, geothermal, and sedimentary basin settings. Carbon dioxide and natural gas have also been released from geologic CO{sub 2} reservoirs and natural gas storage facilities, respectively, due to influences such as well defects and injection/withdrawal processes. These systems serve as natural and industrial analogues for the potential release of CO{sub 2} from geologic storage reservoirs and provide important information about the key features, events, and processes (FEPs) that are associated with releases, as well as the health, safety, and environmental consequences of releases and mitigation efforts that can be applied. We describe a range of natural releases of CO{sub 2} and industrial releases of CO{sub 2} and natural gas in the context of these characteristics. Based on this analysis, several key conclusions can be drawn, and lessons can be learned for geologic carbon storage. First, CO{sub 2} can both accumulate beneath, and be released from, primary and secondary reservoirs with capping units located at a wide range of depths. Both primary and secondary reservoir entrapments for CO{sub 2} should therefore be well characterized at storage sites. Second, many natural releases of CO{sub 2} have been correlated with a specific event that triggered the release, such as magmatic fluid intrusion or seismic activity. The potential for processes that could cause geomechanical damage to sealing cap rocks and trigger the release of CO{sub 2} from a storage

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

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

Lessons from two high CO2 worlds - future oceans and intensive aquaculture.

Science.gov (United States)

Ellis, Robert P; Urbina, Mauricio A; Wilson, Rod W

2017-06-01

Exponentially rising CO 2 (currently ~400 μatm) is driving climate change and causing acidification of both marine and freshwater environments. Physiologists have long known that CO 2 directly affects acid-base and ion regulation, respiratory function and aerobic performance in aquatic animals. More recently, many studies have demonstrated that elevated CO 2 projected for end of this century (e.g. 800-1000 μatm) can also impact physiology, and have substantial effects on behaviours linked to sensory stimuli (smell, hearing and vision) both having negative implications for fitness and survival. In contrast, the aquaculture industry was farming aquatic animals at CO 2 levels that far exceed end-of-century climate change projections (sometimes >10 000 μatm) long before the term 'ocean acidification' was coined, with limited detrimental effects reported. It is therefore vital to understand the reasons behind this apparent discrepancy. Potential explanations include 1) the use of 'control' CO 2 levels in aquaculture studies that go beyond 2100 projections in an ocean acidification context; 2) the relatively benign environment in aquaculture (abundant food, disease protection, absence of predators) compared to the wild; 3) aquaculture species having been chosen due to their natural tolerance to the intensive conditions, including CO 2 levels; or 4) the breeding of species within intensive aquaculture having further selected traits that confer tolerance to elevated CO 2 . We highlight this issue and outline the insights that climate change and aquaculture science can offer for both marine and freshwater settings. Integrating these two fields will stimulate discussion on the direction of future cross-disciplinary research. In doing so, this article aimed to optimize future research efforts and elucidate effective mitigation strategies for managing the negative impacts of elevated CO 2 on future aquatic ecosystems and the sustainability of fish and shellfish

Calcification persists with CO2-induced ocean acidification but decreases with warming for the Caribbean coral Siderastrea siderea

Science.gov (United States)

Castillo, K. D.; Ries, J. B.; Westfield, I. T.; Weiss, J. M.; Bruno, J. F.

2012-12-01

Atmospheric carbon dioxide (pCO2) induced ocean acidification and rising seawater temperatures are identified as two of the greatest threats to modern coral reefs. Within this century, surface seawater pH is expected to decrease by at least 0.3 units, and sea surface temperature is predicted to rise by 1 to 3 °C. However, uncertainty remains as to whether ocean acidification or ocean warming will have a more deleterious impact on coral reefs by the end of the century. Here, we present results of 95-day laboratory experiments in which we investigated the impact of CO2-induced ocean acidification and temperature on the calcification rate of the tropical reef-building zooxanthellate scleractinian coral Siderastrea siderea. We found that calcification rates for S. siderea, estimated from buoyant weighing, increased as pCO2 increased from a pre-industrial value of 324 ppm to a near-present-day value of 477 ppm, remained unchanged as pCO2 increased from 477 ppm to the predicted end-of-century value of 604 ppm, and only declined at 6-times the modern pCO2 value of 2553 ppm. Corals reared at average pCO2 of 488 ppm and at temperatures of 25 and 32 °C, approximately the lower and upper temperature extremes for this species, calcified at lower rates relative to corals reared at 28 °C under equivalent pCO2. These results support the existing evidence that scleractinian corals such as S. siderea are able to manipulate the carbonate chemistry at their calcification site, enabling them to maintain their calcification rates under elevated pCO2 levels predicted for the end of this century. However, exposure of S. siderea corals to sea surface temperatures predicted for tropical waters for the end of this century grossly impaired their rate of calcification. These findings suggest that ocean warming poses a more immediate threat to the coral S. siderea than does ocean acidification, at least under scenarios (B1, A1T, and B2) predicted by the Intergovernmental Panel on Climate

An update to the Surface Ocean CO2 Atlas (SOCAT version 2)

Digital Repository Service at National Institute of Oceanography (India)

Bakker, D.C.E.; Hankin, S.; Olsen, A; Pfeil, B.; Smith, K.; Alin, S.R.; Cosca, C.; Hales, B.; Harasawa, S.; Kozyr, A; Nojiri, Y.; OBrien, K.M.; Schuster, U.; Telszewski, M.; Tilbrook, B.; Wada, C.; Akl, J.; Barbero, L.; Bates, N.; Boutin, J.; Cai, W.J.; Castle, R.D.; Chavez, F.; Chen, L.; Chierici, M.; Currie, K.; Evans, W.; Feely, R.A; Fransson, A; Gao, Z.; Hardman-Mountford, N.; Hoppema, M.; Huang, W.J.; Hunt, C.W.; Huss, B.; Ichikawa, T.; Jacobson, A; Johannessen, T.; Jones, E.M.; Jones, S.; Sara, J.; Kitidis, V.; Kortzinger, A.; Lauvset, S.; Lefevre, N.; Manke, A.B.; Mathis, J.; Metzl, N.; Monteiro, P.; Murata, A.; Newberger, T.; Nobuo, T.; Ono, T.; Paterson, K.; Pierrot, D.; Rios, A.F.; Sabine, C.L.; Saito, S.; Salisbury, J.; Sarma, V.V.S.S.; Schlitzer, R.; Sieger, R.; Skjelvan, I.; Steinhoff, T.; Sullivan, K.; Sutherland, S.C.; Suzuki, T.; Sutton, A.; Sweeney, C.; Takahashi, T.; Tjiputra, J.; VanHeuven, S.; Vandemark, D.; Vlahos, P.; Wallace, D.W.R.; Wanninkhof, R.; Watson, A.J.

of SOCAT is an update of the previous release (version 1) with more data (increased from 6.3 million to 10.1 million surface water fCO₂ values) and extended data coverage (from 1968–2007 to 1968–2011). The quality control criteria, while...

Comparative CO2 flux measurements by eddy covariance technique using open- and closed-path gas analysers over the equatorial Pacific Ocean

Directory of Open Access Journals (Sweden)

Fumiyoshi Kondo

2012-04-01

Full Text Available Direct comparison of air–sea CO2 fluxes by open-path eddy covariance (OPEC and closed-path eddy covariance (CPEC techniques was carried out over the equatorial Pacific Ocean. Previous studies over oceans have shown that the CO2 flux by OPEC was larger than the bulk CO2 flux using the gas transfer velocity estimated by the mass balance technique, while the CO2 flux by CPEC agreed with the bulk CO2 flux. We investigated a traditional conflict between the CO2 flux by the eddy covariance technique and the bulk CO2 flux, and whether the CO2 fluctuation attenuated using the closed-path analyser can be measured with sufficient time responses to resolve small CO2 flux over oceans. Our results showed that the closed-path analyser using a short sampling tube and a high volume air pump can be used to measure the small CO2 fluctuation over the ocean. Further, the underestimated CO2 flux by CPEC due to the attenuated fluctuation can be corrected by the bandpass covariance method; its contribution was almost identical to that of H2O flux. The CO2 flux by CPEC agreed with the total CO2 flux by OPEC with density correction; however, both of them are one order of magnitude larger than the bulk CO2 flux.

Monitoring of ocean storage projects

Energy Technology Data Exchange (ETDEWEB)

Caldeira, K. [Energy and Environment Directorate, Lawrence Livermore National Laboratory, Livermore, CA (United States)

2003-02-01

It has been proposed that atmospheric CO2 accumulation could be slowed by capture of CO2 from point sources and subsequent storage of that CO2 in the ocean. If applied, such sequestration efforts would need to be monitored for compliance, effectiveness, and unintended consequences. Aboveground inspection and monitoring of facilities and practices, combined with ocean observations, could assure compliance with ocean sequestration guidelines and regulations. Ocean observations could be made using a variety of sensors mounted on moorings or underwater gliders. Long-term effectiveness and leakage to the atmosphere must be estimated from models, since on large spatial scales it will be impossible to observationally distinguish carbon stored by a project from variable concentrations of background carbon. Furthermore, the ocean naturally would absorb roughly 80% of fossil fuel CO2 released to the atmosphere within a millennium. This means that most of the CO2 sequestered in the ocean that leaks out to the atmosphere will be reabsorbed by the ocean. However, there is no observational way to distinguish remaining carbon from reabsorbed carbon. The science of monitoring unintended consequences in the deep ocean interior is at a primitive state. Little is understood about ecosystems of the deep ocean interior; and even less is understood about how those ecosystems would respond to added CO2. High priority research objectives should be (1) to improve our understanding of the natural ecosystems of the deep ocean, and (2) to improve our understanding of the response of these ecosystems to increased oceanic CO2 concentrations and decreased ocean pH.

Risk assessment of excessive CO_2 emission on diatom heavy metal consumption

International Nuclear Information System (INIS)

Liu, Fengjiao; Li, Shunxing; Zheng, Fengying; Huang, Xuguang

2016-01-01

Diatoms are the dominant group of phytoplankton in the modern ocean, accounting for approximately 40% of oceanic primary productivity and critical foundation of coastal food web. Rising dissolution of anthropogenic CO_2 in seawater may directly/indirectly cause ocean acidification and desalination. However, little is known about dietary diatom-associated changes, especially for diatom heavy metal consumption sensitivity to these processes, which is important for seafood safety and nutrition assessment. Here we show some links between ocean acidification/desalination and heavy metal consumption by Thalassiosira weissflogii. Excitingly, under desalination stress, the relationships between Cu, Zn, and Cd were all positively correlated, especially between Cu and Zn (r = 0.989, total intracellular concentration) and between Zn and Cd (r = 0.962, single-cell intracellular concentration). Heavy metal consumption activity in decreasing order was acidification < acidification + desalination < desalination for Zn, acidification < desalination < acidification + desalination for Cu and Cd, i.e., heavy metal uptake (or release) were controlled by environmental stress. Our findings showed that heavy metal uptake (or release) was already responded to ongoing excessive CO_2 emission-driven acidification and desalination, which was important for risk assessment of climate change on diatom heavy metal consumption, food web and then seafood safety in future oceans. - Highlights: • Excessive CO_2 in seawater may causes ocean acidification and desalination. • The relationships between Cu, Zn, and Cd were all positively correlated by desalination. • Significant effects of salinity on intracellular concentration of Cu and Cd • Cu and Cd in marine phytoplankton could be regulated by metal excretion. • Heavy metal consumption was affect by excessive CO_2.

Giant Clams and Rising CO2: Light May Ameliorate Effects of Ocean Acidification on a Solar-Powered Animal.

Directory of Open Access Journals (Sweden)

Sue-Ann Watson

Full Text Available Global climate change and ocean acidification pose a serious threat to marine life. Marine invertebrates are particularly susceptible to ocean acidification, especially highly calcareous taxa such as molluscs, echinoderms and corals. The largest of all bivalve molluscs, giant clams, are already threatened by a variety of local pressures, including overharvesting, and are in decline worldwide. Several giant clam species are listed as 'Vulnerable' on the IUCN Red List of Threatened Species and now climate change and ocean acidification pose an additional threat to their conservation. Unlike most other molluscs, giant clams are 'solar-powered' animals containing photosynthetic algal symbionts suggesting that light could influence the effects of ocean acidification on these vulnerable animals. In this study, juvenile fluted giant clams Tridacna squamosa were exposed to three levels of carbon dioxide (CO2 (control ~400, mid ~650 and high ~950 μatm and light (photosynthetically active radiation 35, 65 and 304 μmol photons m-2 s-1. Elevated CO2 projected for the end of this century (~650 and ~950 μatm reduced giant clam survival and growth at mid-light levels. However, effects of CO2 on survival were absent at high-light, with 100% survival across all CO2 levels. Effects of CO2 on growth of surviving clams were lessened, but not removed, at high-light levels. Shell growth and total animal mass gain were still reduced at high-CO2. This study demonstrates the potential for light to alleviate effects of ocean acidification on survival and growth in a threatened calcareous marine invertebrate. Managing water quality (e.g. turbidity and sedimentation in coastal areas to maintain water clarity may help ameliorate some negative effects of ocean acidification on giant clams and potentially other solar-powered calcifiers, such as hard corals.

Giant Clams and Rising CO2: Light May Ameliorate Effects of Ocean Acidification on a Solar-Powered Animal.

Science.gov (United States)

Watson, Sue-Ann

2015-01-01

Global climate change and ocean acidification pose a serious threat to marine life. Marine invertebrates are particularly susceptible to ocean acidification, especially highly calcareous taxa such as molluscs, echinoderms and corals. The largest of all bivalve molluscs, giant clams, are already threatened by a variety of local pressures, including overharvesting, and are in decline worldwide. Several giant clam species are listed as 'Vulnerable' on the IUCN Red List of Threatened Species and now climate change and ocean acidification pose an additional threat to their conservation. Unlike most other molluscs, giant clams are 'solar-powered' animals containing photosynthetic algal symbionts suggesting that light could influence the effects of ocean acidification on these vulnerable animals. In this study, juvenile fluted giant clams Tridacna squamosa were exposed to three levels of carbon dioxide (CO2) (control ~400, mid ~650 and high ~950 μatm) and light (photosynthetically active radiation 35, 65 and 304 μmol photons m-2 s-1). Elevated CO2 projected for the end of this century (~650 and ~950 μatm) reduced giant clam survival and growth at mid-light levels. However, effects of CO2 on survival were absent at high-light, with 100% survival across all CO2 levels. Effects of CO2 on growth of surviving clams were lessened, but not removed, at high-light levels. Shell growth and total animal mass gain were still reduced at high-CO2. This study demonstrates the potential for light to alleviate effects of ocean acidification on survival and growth in a threatened calcareous marine invertebrate. Managing water quality (e.g. turbidity and sedimentation) in coastal areas to maintain water clarity may help ameliorate some negative effects of ocean acidification on giant clams and potentially other solar-powered calcifiers, such as hard corals.

Gas hydrate dissociation prolongs acidification of the Anthropocene oceans

OpenAIRE

Boudreau, B.P.; Luo, Y.; Meysman, F.J.R.; Middelburg, J

2015-01-01

Anthropogenic warming of the oceans can release methane (CH4) currently stored in sediments as gas hydrates. This CH4 will be oxidized to CO2, thus increasing the acidification of the oceans. We employ a biogeochemical model of the multimillennial carbon cycle to determine the evolution of the oceanic dissolved carbonate system over the next 13?kyr in response to CO2 from gas hydrates, combined with a reasonable scenario for long-term anthropogenic CO2 emissions. Hydrate-derived CO2 will appr...

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...

The fate of pelagic CaCO3 production in a high CO2 ocean: a model study

Directory of Open Access Journals (Sweden)

C. Ethe

2007-07-01

Full Text Available This model study addresses the change in pelagic calcium carbonate production (CaCO3, as calcite in the model and dissolution in response to rising atmospheric CO2. The parameterization of CaCO3 production includes a dependency on the saturation state of seawater with respect to calcite. It was derived from laboratory and mesocosm studies on particulate organic and inorganic carbon production in Emiliania huxleyi as a function of pCO2. The model predicts values of CaCO3 production and dissolution in line with recent estimates. The effect of rising pCO2 on CaCO3 production and dissolution was quantified by means of model simulations forced with atmospheric CO2 increasing at a rate of 1% per year from 286 ppm to 1144 ppm over a 140 year time-period. The simulation predicts a decrease of CaCO3 production by 27%. The combined change in production and dissolution of CaCO3 yields an excess uptake of CO2 from the atmosphere by the ocean of 5.9 GtC over the period of 140 years.

Laboratory Investigations in Support of Dioxide-Limestone Sequestration in the Ocean

Energy Technology Data Exchange (ETDEWEB)

Dan Golomb; Eugene Barry; David Ryan; Stephen Pennell; Carl Lawton; Peter Swett; Devinder Arora; John Hannon; Michael Woods; Huishan Duan; Tom Lawlor

2008-09-30

that the CaCO{sub 3} emulsion is slightly alkaline, not acidic. We tested the release of the CO{sub 2}-in-H{sub 2}O emulsion stabilized by pulverized limestone in the DOE National Energy Technology Laboratory High Pressure Water Tunnel Facility (HPWTF). Digital photographs showed the sinking globules in the HPWTF, confirming the concept of releasing the emulsion in the deep ocean. We modeled the release of an emulsion from the CO{sub 2} output of a 1000 MW coal-fired power plant at 500 m depth. The emulsion would typically sink several hundred meters before density equilibration with ambient seawater. The CO{sub 2} globules would rain out from the equilibrated plume toward the ocean bottom where they would disintegrate due to wave action and bottom friction. Conceptual release systems are described both for an open ocean release and a sloping seabed release of the emulsion.

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.

Empirical methods for the estimation of Southern Ocean CO2: support vector and random forest regression

CSIR Research Space (South Africa)

Gregor, Luke

2017-12-01

Full Text Available understanding with spatially integrated air–sea flux estimates (Fay and McKinley, 2014). Conversely, ocean biogeochemical process models are good tools for mechanis- tic understanding, but fail to represent the seasonality of CO2 fluxes in the Southern Ocean... of including coordinate variables as proxies of 1pCO2 in the empirical methods. In the inter- comparison study by Rödenbeck et al. (2015) proxies typi- cally include, but are not limited to, sea surface temperature (SST), chlorophyll a (Chl a), mixed layer...

Risk assessment of excessive CO{sub 2} emission on diatom heavy metal consumption

Energy Technology Data Exchange (ETDEWEB)

Liu, Fengjiao; Li, Shunxing, E-mail: shunxing_li@aliyun.com; Zheng, Fengying; Huang, Xuguang

2016-10-01

Diatoms are the dominant group of phytoplankton in the modern ocean, accounting for approximately 40% of oceanic primary productivity and critical foundation of coastal food web. Rising dissolution of anthropogenic CO{sub 2} in seawater may directly/indirectly cause ocean acidification and desalination. However, little is known about dietary diatom-associated changes, especially for diatom heavy metal consumption sensitivity to these processes, which is important for seafood safety and nutrition assessment. Here we show some links between ocean acidification/desalination and heavy metal consumption by Thalassiosira weissflogii. Excitingly, under desalination stress, the relationships between Cu, Zn, and Cd were all positively correlated, especially between Cu and Zn (r = 0.989, total intracellular concentration) and between Zn and Cd (r = 0.962, single-cell intracellular concentration). Heavy metal consumption activity in decreasing order was acidification < acidification + desalination < desalination for Zn, acidification < desalination < acidification + desalination for Cu and Cd, i.e., heavy metal uptake (or release) were controlled by environmental stress. Our findings showed that heavy metal uptake (or release) was already responded to ongoing excessive CO{sub 2} emission-driven acidification and desalination, which was important for risk assessment of climate change on diatom heavy metal consumption, food web and then seafood safety in future oceans. - Highlights: • Excessive CO{sub 2} in seawater may causes ocean acidification and desalination. • The relationships between Cu, Zn, and Cd were all positively correlated by desalination. • Significant effects of salinity on intracellular concentration of Cu and Cd • Cu and Cd in marine phytoplankton could be regulated by metal excretion. • Heavy metal consumption was affect by excessive CO{sub 2}.

Regional contributions of ocean iron fertilization to atmospheric CO2 changes during the last glacial termination

Science.gov (United States)

Opazo, N. E.; Lambert, F.

2017-12-01

Mineral dust aerosols affect climate directly by changing the radiative balance of the Earth, and indirectly by acting as cloud condensation nuclei and by affecting biogeochemical cycles. The impact on marine biogeochemical cycles is primarily through the supply of micronutrients such as iron to nutrient-limited regions of the oceans. Iron fertilization of High Nutrient Low Chlorophyll (HNLC) regions of the oceans is thought to have significantly affected the carbon cycle on glacial-interglacial scales and contributed about one fourth of the 80-100 ppm lowering of glacial atmospheric CO2 concentrations.In this study, we quantify the effect of global dust fluxes on atmospheric CO2 using the cGENIE model, an Earth System Model of Intermediate Complexity with emphasis on the carbon cycle. Global Holocene and Last Glacial Maximum (LGM) dust flux fields were obtained from both dust model simulations and reconstructions based on observational data. The analysis was performed in two stages. In the first instance, we produced 8 global intermediate dust flux fields between Holocene and LGM and simulated the atmospheric CO2 drawdown due to these 10 dust levels. In the second stage, we only changed dust flux levels in specific HNLC regions to isolate the effect of these ocean basins. We thus quantify the contribution of the South Atlantic, the South Pacific, the North Pacific, and the Central Pacific HNLC regions to the total atmospheric CO2 difference due to iron fertilization of the Earth's oceans.

CO2-level Dependent Effects of Ocean Acidification on Squid, Doryteuthis pealeii, Early Life History

KAUST Repository

Zakroff, Casey J.

2013-12-01

Ocean acidification is predicted to lead to global oceanic decreases in pH of up to 0.3 units within the next 100 years. However, those levels are already being reached currently in coastal regions due to natural CO2 variability. Squid are a vital component of the pelagic ecosystem, holding a unique niche as a highly active predatory invertebrate and major prey stock for upper trophic levels. This study examined the effects of a range of ocean acidification regimes on the early life history of a coastal squid species, the Atlantic longfin squid, Doryteuthis pealeii. Eggs were raised in a flow-through ocean acidification system at CO2 levels ranging from ambient (400ppm) to 2200ppm. Time to hatching, hatching efficiency, and hatchling mantle lengths, yolk sac sizes, and statoliths were all examined to elucidate stress effects. Delays in hatching time of at least a day were seen at exposures above 1300ppm in all trials under controlled conditions. Mantle lengths were significantly reduced at exposures above 1300 ppm. Yolk sac sizes varied between CO2 treatments, but no distinct pattern emerged. Statoliths were increasingly porous and malformed as CO2 exposures increased, and were significantly reduced in surface area at exposures above 1300ppm. Doryteuthis pealeii appears to be able to withstand acidosis stress without major effects up to 1300ppm, but is strongly impacted past that threshold. Since yolk consumption did not vary among treatments, it appears that during its early life stages, D. pealeii reallocates its available energy budget away from somatic growth and system development in order to mitigate the stress of acidosis.

Process design of a new injection method of liquid CO2 at the intermediate depths in the ocean using a static mixer

International Nuclear Information System (INIS)

Tajima, Hideo; Yamasaki, Akihiro; Kiyono, Fumio

2005-01-01

Process design for a new injection method of liquid CO 2 using a static mixer was conducted based on laboratory experimental results on the formation process of liquid CO 2 drops covered with hydrate film by a Kenics-type static mixer, and numerical simulation of the liquid CO 2 drops at 500 and 1500 m. The Sauter Mean Diameter (SMD) of the liquid CO 2 drops covered with hydrate film was dramatically decreased with the use of the static mixer; empirical equations were obtained for the SMD, and also the maximum and minimum diameters of the liquid CO 2 drops for a given flow velocity (Weber number, We). The ascending and dissolving behavior of a liquid CO 2 drop with hydrate released in the ocean at an intermediate depth was numerically simulated, and the maximum drop diameter to avoid evaporation of the drop before complete dissolution was estimated. Based on these results, scaling up of the static mixer was conducted by assuming a disposal process of CO 2 emitted from a 100-MW thermal power plant, and the mixer diameter was determined as a function of the given SMD. Moreover, the power consumption of the static mixer was evaluated and found to be almost negligible. (author)

Evaluation of Release-05 GRACE time-variable gravity coefficients over the ocean

Directory of Open Access Journals (Sweden)

D. P. Chambers

2012-10-01

Full Text Available The latest release of GRACE (Gravity Recovery and Climate Experiment gravity field coefficients (Release-05, or RL05 are evaluated for ocean applications. Data have been processed using the current methodology for Release-04 (RL04 coefficients, and have been compared to output from two different ocean models. Results indicate that RL05 data from the three Science Data Centers – the Center for Space Research (CSR, GeoForschungsZentrum (GFZ, and Jet Propulsion Laboratory (JPL – are more consistent among themselves than the previous RL04 data. Moreover, the variance of residuals with the output of an ocean model is 50–60% lower for RL05 data than for RL04 data. A more optimized destriping algorithm is also tested, which improves the results slightly. By comparing the GRACE maps with two different ocean models, we can better estimate the uncertainty in the RL05 maps. We find the standard error to be about 1 cm (equivalent water thickness in the low- and mid-latitudes, and between 1.5 and 2 cm in the polar and subpolar oceans, which is comparable to estimated uncertainty for the output from the ocean models.

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...

Response of bacterioplankton community structure to an artificial gradient of pCO2 in the Arctic Ocean

Directory of Open Access Journals (Sweden)

R. Zhang

2013-06-01

Full Text Available In order to test the influences of ocean acidification on the ocean pelagic ecosystem, so far the largest CO2 manipulation mesocosm study (European Project on Ocean Acidification, EPOCA was performed in Kings Bay (Kongsfjorden, Spitsbergen. During a 30 day incubation, bacterial diversity was investigated using DNA fingerprinting and clone library analysis of bacterioplankton samples. Terminal restriction fragment length polymorphism (T-RFLP analysis of the PCR amplicons of the 16S rRNA genes revealed that general bacterial diversity, taxonomic richness and community structure were influenced by the variation of productivity during the time of incubation, but not the degree of ocean acidification. A BIOENV analysis suggested a complex control of bacterial community structure by various biological and chemical environmental parameters. The maximum apparent diversity of bacterioplankton (i.e., the number of T-RFs in high and low pCO2 treatments differed significantly. A negative relationship between the relative abundance of Bacteroidetes and pCO2 levels was observed for samples at the end of the experiment by the combination of T-RFLP and clone library analysis. Our study suggests that ocean acidification affects the development of bacterial assemblages and potentially impacts the ecological function of the bacterioplankton in the marine ecosystem.

Response of bacterioplankton community structure to an artificial gradient of pCO2 in the Arctic Ocean

Science.gov (United States)

Zhang, R.; Xia, X.; Lau, S. C. K.; Motegi, C.; Weinbauer, M. G.; Jiao, N.

2013-06-01

In order to test the influences of ocean acidification on the ocean pelagic ecosystem, so far the largest CO2 manipulation mesocosm study (European Project on Ocean Acidification, EPOCA) was performed in Kings Bay (Kongsfjorden), Spitsbergen. During a 30 day incubation, bacterial diversity was investigated using DNA fingerprinting and clone library analysis of bacterioplankton samples. Terminal restriction fragment length polymorphism (T-RFLP) analysis of the PCR amplicons of the 16S rRNA genes revealed that general bacterial diversity, taxonomic richness and community structure were influenced by the variation of productivity during the time of incubation, but not the degree of ocean acidification. A BIOENV analysis suggested a complex control of bacterial community structure by various biological and chemical environmental parameters. The maximum apparent diversity of bacterioplankton (i.e., the number of T-RFs) in high and low pCO2 treatments differed significantly. A negative relationship between the relative abundance of Bacteroidetes and pCO2 levels was observed for samples at the end of the experiment by the combination of T-RFLP and clone library analysis. Our study suggests that ocean acidification affects the development of bacterial assemblages and potentially impacts the ecological function of the bacterioplankton in the marine ecosystem.

Comparative CO{sub 2} flux measurements by eddy covariance technique using open- and closed-path gas analysers over the equatorial Pacific Ocean

Energy Technology Data Exchange (ETDEWEB)

Kondo, Fumiyoshi (Graduate School of Natural Science and Technology, Okayama Univ., Okayama (Japan); Atmosphere and Ocean Research Inst., Univ. of Tokyo, Tokyo (Japan)), Email: fkondo@aori.u-tokyo.ac.jp; Tsukamoto, Osamu (Graduate School of Natural Science and Technology, Okayama Univ., Okayama (Japan))

2012-04-15

Direct comparison of airsea CO{sub 2} fluxes by open-path eddy covariance (OPEC) and closed-path eddy covariance (CPEC) techniques was carried out over the equatorial Pacific Ocean. Previous studies over oceans have shown that the CO{sub 2} flux by OPEC was larger than the bulk CO{sub 2} flux using the gas transfer velocity estimated by the mass balance technique, while the CO{sub 2} flux by CPEC agreed with the bulk CO{sub 2} flux. We investigated a traditional conflict between the CO{sub 2} flux by the eddy covariance technique and the bulk CO{sub 2} flux, and whether the CO{sub 2} fluctuation attenuated using the closed-path analyser can be measured with sufficient time responses to resolve small CO{sub 2} flux over oceans. Our results showed that the closed-path analyser using a short sampling tube and a high volume air pump can be used to measure the small CO{sub 2} fluctuation over the ocean. Further, the underestimated CO{sub 2} flux by CPEC due to the attenuated fluctuation can be corrected by the bandpass covariance method; its contribution was almost identical to that of H{sub 2}O flux. The CO{sub 2} flux by CPEC agreed with the total CO{sub 2} flux by OPEC with density correction; however, both of them are one order of magnitude larger than the bulk CO{sub 2} flux

Carbon dioxide exchange between atmosphere and ocean and the question of an increase of atmospheric CO/sub 2/ during the past decades

Energy Technology Data Exchange (ETDEWEB)

Revelle, R; Suess, H E

1957-01-01

From a comparison of C/sup 14//C/sup 12/ and C/sup 13//C/sup 12/ ratios in wood and in marine material and from a slight decrease of the C/sup 14/ concentration in terrestrial plants over the past 50 years it can be concluded that the average lifetime of a CO/sub 2/ molecule in the atmosphere before it is dissolved into the sea is of the order of 10 years. This means that most of the CO/sub 2/ released by artificial fuel combustion since the beginning of the industrial revolution must have been absorbed by the oceans. The increase of atmospheric CO/sub 2/ from this cause is at present small but may become significant during future decades of industrial fuel combustion continues to rise exponentially. Present data on the total amount of CO/sub 2/ in the atmosphere, on the rates and mechanisms of exchange, and on possible fluctuations in terrestrial and marine organic carbon, are inadequate for accurate measurement of future changes in atmospheric CO/sub 2/. An opportunity exists during the international geophysical year to obtain much of the necessary information.

Acute physiological impacts of CO2 ocean sequestration on marine animals

International Nuclear Information System (INIS)

Ishimatsu, A.; Hayashi, M.; Lee, K.S.; Murata, K.; Kumagai, E.

2005-01-01

The biological impacts of ocean carbon dioxide (CO 2 ) sequestration must be carefully considered before it is implemented as a mitigation strategy. This paper presented details of a study investigating the effects of high CO 2 concentrations on marine fish, lobster, and octopus. The influence of water temperature on the physiological effects of CO 2 was also discussed. In the first part of the study, eggs and larvae of red seabream were exposed to both CO 2 and HCI-acidified seawater at identical pH levels. Seabream in the CO 2 group showed a much higher mortality rate than fish in the HCI group. Other tests showed that Japanese Flounder died after complete recovery of pH in seawater equilibrated with 5 per cent CO 2 . Cardiac output was rapidly depressed in Yellowtail fish without significant changes in blood oxygen concentrations. Lower temperatures resulted in higher mortality and delayed pH recovery during hypercapnia in all fish. Western rock lobsters were the most tolerant to CO 2 among all species tested. The recovery of hemolymph pH was complete at exposure to CO 2 concentrations of 1 per cent. Changes in hemolymph bicarbonate concentrations indicated that acid-based regulatory mechanisms differed between fish and lobsters. Mortality rates for octopus were significant at CO 2 concentrations of 1 per cent. The results of all tests showed that aquatic animals are more susceptible to increases in ambient CO 2 levels than terrestrial animals. It was concluded that even slight elevations in CO 2 concentration levels adversely affected physiological functioning in the tested species. It was concluded that CO 2 sequestration in deeper, colder waters will have a more pronounced effect on aquatic animals due to the interactions between CO 2 and lower temperatures, as well as the fact that most deep-sea fish are less tolerant to environmental perturbations. 3 refs., 1 tab., 3 figs

Ocean acidification and responses to predators: can sensory redundancy reduce the apparent impacts of elevated CO2 on fish?

Science.gov (United States)

Lönnstedt, Oona M; Munday, Philip L; McCormick, Mark I; Ferrari, Maud C O; Chivers, Douglas P

2013-09-01

Carbon dioxide (CO2) levels in the atmosphere and surface ocean are rising at an unprecedented rate due to sustained and accelerating anthropogenic CO2 emissions. Previous studies have documented that exposure to elevated CO2 causes impaired antipredator behavior by coral reef fish in response to chemical cues associated with predation. However, whether ocean acidification will impair visual recognition of common predators is currently unknown. This study examined whether sensory compensation in the presence of multiple sensory cues could reduce the impacts of ocean acidification on antipredator responses. When exposed to seawater enriched with levels of CO2 predicted for the end of this century (880 μatm CO2), prey fish completely lost their response to conspecific alarm cues. While the visual response to a predator was also affected by high CO2, it was not entirely lost. Fish exposed to elevated CO2, spent less time in shelter than current-day controls and did not exhibit antipredator signaling behavior (bobbing) when multiple predator cues were present. They did, however, reduce feeding rate and activity levels to the same level as controls. The results suggest that the response of fish to visual cues may partially compensate for the lack of response to chemical cues. Fish subjected to elevated CO2 levels, and exposed to chemical and visual predation cues simultaneously, responded with the same intensity as controls exposed to visual cues alone. However, these responses were still less than control fish simultaneously exposed to chemical and visual predation cues. Consequently, visual cues improve antipredator behavior of CO2 exposed fish, but do not fully compensate for the loss of response to chemical cues. The reduced ability to correctly respond to a predator will have ramifications for survival in encounters with predators in the field, which could have repercussions for population replenishment in acidified oceans.

Connexin hemichannel-mediated CO2-dependent release of ATP in the medulla oblongata contributes to central respiratory chemosensitivity

Science.gov (United States)

Huckstepp, Robert T R; id Bihi, Rachid; Eason, Robert; Spyer, K Michael; Dicke, Nikolai; Willecke, Klaus; Marina, Nephtali; Gourine, Alexander V; Dale, Nicholas

2010-01-01

Arterial , a major determinant of breathing, is detected by chemosensors located in the brainstem. These are important for maintaining physiological levels of in the blood and brain, yet the mechanisms by which the brain senses CO2 remain controversial. As ATP release at the ventral surface of the brainstem has been causally linked to the adaptive changes in ventilation in response to hypercapnia, we have studied the mechanisms of CO2-dependent ATP release in slices containing the ventral surface of the medulla oblongata. We found that CO2-dependent ATP release occurs in the absence of extracellular acidification and correlates directly with the level of . ATP release is independent of extracellular Ca2+ and may occur via the opening of a gap junction hemichannel. As agents that act on connexin channels block this release, but compounds selective for pannexin-1 have no effect, we conclude that a connexin hemichannel is involved in CO2-dependent ATP release. We have used molecular, genetic and immunocytochemical techniques to demonstrate that in the medulla oblongata connexin 26 (Cx26) is preferentially expressed near the ventral surface. The leptomeninges, subpial astrocytes and astrocytes ensheathing penetrating blood vessels at the ventral surface of the medulla can be loaded with dye in a CO2-dependent manner, suggesting that gating of a hemichannel is involved in ATP release. This distribution of CO2-dependent dye loading closely mirrors that of Cx26 expression and colocalizes to glial fibrillary acidic protein (GFAP)-positive cells. In vivo, blockers with selectivity for Cx26 reduce hypercapnia-evoked ATP release and the consequent adaptive enhancement of breathing. We therefore propose that Cx26-mediated release of ATP in response to changes in is an important mechanism contributing to central respiratory chemosensitivity. PMID:20736421

Temperature dependence of CO2-enhanced primary production in the European Arctic Ocean

KAUST Repository

Holding, J. M.; Duarte, Carlos M.; Sanz-Martí n, M.; Mesa, E.; Arrieta, J M; Chierici, M.; Hendriks, I.  E.; Garcí a-Corral, L. S.; Regaudie-de-Gioux, A.; Delgado, A.; Reigstad, M.; Wassmann, P.; Agusti, Susana

2015-01-01

production (GPP) may be temperature dependent, using data from several oceanographic cruises and experiments from both spring and summer in the European sector of the Arctic Ocean. Results confirm that CO2 enhances GPP (by a factor of up to ten) over a range

Effect of land albedo, CO2, orography, and oceanic heat transport on extreme climates

Directory of Open Access Journals (Sweden)

V. Romanova

2006-01-01

Full Text Available Using an atmospheric general circulation model of intermediate complexity coupled to a sea ice – slab ocean model, we perform a number of sensitivity experiments under present-day orbital conditions and geographical distribution to assess the possibility that land albedo, atmospheric CO2, orography and oceanic heat transport may cause an ice-covered Earth. Changing only one boundary or initial condition, the model produces solutions with at least some ice-free oceans in the low latitudes. Using some combination of these forcing parameters, a full Earth's glaciation is obtained. We find that the most significant factor leading to an ice-covered Earth is the high land albedo in combination with initial temperatures set equal to the freezing point. Oceanic heat transport and orography play only a minor role for the climate state. Extremely low concentrations of CO2 also appear to be insufficient to provoke a runaway ice-albedo feedback, but the strong deviations in surface air temperatures in the Northern Hemisphere point to the existence of a strong nonlinearity in the system. Finally, we argue that the initial condition determines whether the system can go into a completely ice covered state, indicating multiple equilibria, a feature known from simple energy balance models.

1.5 My benthic foraminiferal B/Ca record of carbonate chemistry in the deep Atlantic: Implications for ocean alkalinity and atmospheric CO2

Science.gov (United States)

Rosenthal, Y.; Sosdian, S. M.; Toggweiler, J. R.

2017-12-01

Most hypotheses to explain glacial-interglacial changes in atmospheric CO2 invoke shifts in ocean alkalinity explain roughly half the reduction in glacial CO2 via CaCO3 compensatory mechanism. It follows that changes in CaCO3 burial occur in response to an increase in deep ocean respired carbon content. To date our understanding of this process comes from benthic carbon isotope and %CaCO3 records. However, to understand the nature of the ocean's buffering capacity and its role in modulating pCO2, orbitally resolved reconstructions of the deep ocean carbonate system parameters are necessary. Here we present a 1.5 Myr orbitally resolved deep ocean calcite saturation record (ΔCO32-) derived from benthic foraminiferal B/Ca ratios in the North Atlantic. Glacial B/Ca values decline across the mid-Pleistocene transition (MPT) suggesting increased sequestration of carbon in the deep Atlantic. The magnitude, timing, and structure of deep Atlantic Ocean ΔCO32- and %CaCO3 cycles contrast with the small amplitude, anti-phased swings in IndoPacific ΔCO32- and %CaCO3 during the mid-to-late Pleistocene. Increasing corrosivity of the deep Atlantic causes the locus of CaCO3 burial to shift into the equatorial Pacific where the flux of CaCO3 to the seafloor is high enough to establish and maintain a new "hot spot". We propose that the CO32- in the deep IndoPacific rises in response to the same mechanism that keeps the CO32- in the deep Atlantic low and the atmospheric CO2 low. The increase in interglacial atmospheric pCO2 levels following the Mid-Brunhes event ( 400ka) are associated with increased G/IG ΔCO3 amplitude, expressed by a decrease in the glacial ΔCO32- values. We propose the low persistent ΔCO32- levels at Marine Isotope Stage (MIS) 12 set the stage for the high pCO2 levels at MIS 11 via an increase in whole ocean alkalinity followed by enhanced CaCO3 preservation. Based on this, we suggest that the development of classic (`anticorrelated') CaCO3 patterns was

Chloride cells as an index of the impacts of CO{sub 2} ocean sequestration on marine fish

Energy Technology Data Exchange (ETDEWEB)

Hayashi, M.; Ishimatsu, A. [Nagasaki Univ., Nagasaki (Japan). Marine Research Inst.; Kikkawa, T. [Nagasaki Univ., Nagasaki (Japan). Marine Research Inst.]|[Marine Ecology Research Inst., Onjuku, Chiba (Japan). Central Laboratory

2005-07-01

Carbon dioxide (CO{sub 2}) ocean sequestration has been proposed as a potential measure to mitigate greenhouse gas emissions to the atmosphere. However, the impacts of CO{sub 2} ocean sequestration on marine organisms must be examined in discussing the feasibility of this mitigation measure. This study examined the changes in the morphology of chloride cells (CCs) and activity of Na{sup +}, K{sup +} -ATPase of the Japanese flounder Paralichthys olivaceus during aquatic hypercapnia. The apical openings area increased 1.3 and 4.1 times in 24 hour exposures to 1 per cent and 5 per cent CO{sub 2}, respectively, while the CCs area or density did not change at both concentrations. Gill Na{sup +}, K{sup +} -ATPase activity more than doubled at 72 hours and then decreased at 1 per cent CO{sub 2}, whereas it increased to 170 per cent at 24 hours during exposure to 5 per cent CO{sub 2} . These results suggest that branchial CCs are involved in acid-base regulation in marine fish under environmental hypercapnia. 4 refs., 2 figs.

Burrows of the Semi-Terrestrial Crab Ucides cordatus Enhance CO2 Release in a North Brazilian Mangrove Forest

Science.gov (United States)

Pülmanns, Nathalie; Diele, Karen; Mehlig, Ulf; Nordhaus, Inga

2014-01-01

Ucides cordatus is an abundant mangrove crab in Brazil constructing burrows of up to 2 m depth. Sediment around burrows may oxidize during low tides. This increase in sediment-air contact area may enhance carbon degradation processes. We hypothesized that 1) the sediment CO2 efflux rate is greater with burrows than without and 2) the reduction potential in radial profiles in the sediment surrounding the burrows decreases gradually, until approximating non-bioturbated conditions. Sampling was conducted during the North Brazilian wet season at neap tides. CO2 efflux rates of inhabited burrows and plain sediment were measured with a CO2/H2O gas analyzer connected to a respiration chamber. Sediment redox potential, pH and temperature were measured in the sediment surrounding the burrows at horizontal distances of 2, 5, 8 and 15 cm at four sediment depths (1, 10, 30 and 50 cm) and rH values were calculated. Sediment cores (50 cm length) were taken to measure the same parameters for plain sediment. CO2 efflux rates of plain sediment and individual crab burrows with entrance diameters of 7 cm were 0.7–1.3 µmol m−2 s−1 and 0.2–0.4 µmol burrows−1 s−1, respectively. CO2 released from a Rhizophora mangle dominated forest with an average of 1.7 U. cordatus burrows−1 m−2 yielded 1.0–1.7 µmol m−2 s−1, depending on the month and burrow entrance diameter. Laboratory experiments revealed that 20–60% of the CO2 released by burrows originated from crab respiration. Temporal changes in the reduction potential in the sediment surrounding the burrows did not influence the CO2 release from burrows. More oxidized conditions of plain sediment over time may explain the increase in CO2 release until the end of the wet season. CO2 released by U. cordatus and their burrows may be a significant pathway of CO2 export from mangrove sediments and should be considered in mangrove carbon budget estimates. PMID:25313661

Burrows of the semi-terrestrial crab Ucides cordatus enhance CO2 release in a North Brazilian mangrove forest.

Directory of Open Access Journals (Sweden)

Nathalie Pülmanns

Full Text Available Ucides cordatus is an abundant mangrove crab in Brazil constructing burrows of up to 2 m depth. Sediment around burrows may oxidize during low tides. This increase in sediment-air contact area may enhance carbon degradation processes. We hypothesized that 1 the sediment CO2 efflux rate is greater with burrows than without and 2 the reduction potential in radial profiles in the sediment surrounding the burrows decreases gradually, until approximating non-bioturbated conditions. Sampling was conducted during the North Brazilian wet season at neap tides. CO2 efflux rates of inhabited burrows and plain sediment were measured with a CO2/H2O gas analyzer connected to a respiration chamber. Sediment redox potential, pH and temperature were measured in the sediment surrounding the burrows at horizontal distances of 2, 5, 8 and 15 cm at four sediment depths (1, 10, 30 and 50 cm and rH values were calculated. Sediment cores (50 cm length were taken to measure the same parameters for plain sediment. CO2 efflux rates of plain sediment and individual crab burrows with entrance diameters of 7 cm were 0.7-1.3 µmol m(-2 s(-1 and 0.2-0.4 µmol burrows(-1 s(-1, respectively. CO2 released from a Rhizophora mangle dominated forest with an average of 1.7 U. cordatus burrows(-1 m(-2 yielded 1.0-1.7 µmol m(-2 s(-1, depending on the month and burrow entrance diameter. Laboratory experiments revealed that 20-60% of the CO2 released by burrows originated from crab respiration. Temporal changes in the reduction potential in the sediment surrounding the burrows did not influence the CO2 release from burrows. More oxidized conditions of plain sediment over time may explain the increase in CO2 release until the end of the wet season. CO2 released by U. cordatus and their burrows may be a significant pathway of CO2 export from mangrove sediments and should be considered in mangrove carbon budget estimates.

Burrows of the semi-terrestrial crab Ucides cordatus enhance CO2 release in a North Brazilian mangrove forest.

Science.gov (United States)

Pülmanns, Nathalie; Diele, Karen; Mehlig, Ulf; Nordhaus, Inga

2014-01-01

Ucides cordatus is an abundant mangrove crab in Brazil constructing burrows of up to 2 m depth. Sediment around burrows may oxidize during low tides. This increase in sediment-air contact area may enhance carbon degradation processes. We hypothesized that 1) the sediment CO2 efflux rate is greater with burrows than without and 2) the reduction potential in radial profiles in the sediment surrounding the burrows decreases gradually, until approximating non-bioturbated conditions. Sampling was conducted during the North Brazilian wet season at neap tides. CO2 efflux rates of inhabited burrows and plain sediment were measured with a CO2/H2O gas analyzer connected to a respiration chamber. Sediment redox potential, pH and temperature were measured in the sediment surrounding the burrows at horizontal distances of 2, 5, 8 and 15 cm at four sediment depths (1, 10, 30 and 50 cm) and rH values were calculated. Sediment cores (50 cm length) were taken to measure the same parameters for plain sediment. CO2 efflux rates of plain sediment and individual crab burrows with entrance diameters of 7 cm were 0.7-1.3 µmol m(-2) s(-1) and 0.2-0.4 µmol burrows(-1) s(-1), respectively. CO2 released from a Rhizophora mangle dominated forest with an average of 1.7 U. cordatus burrows(-1) m(-2) yielded 1.0-1.7 µmol m(-2) s(-1), depending on the month and burrow entrance diameter. Laboratory experiments revealed that 20-60% of the CO2 released by burrows originated from crab respiration. Temporal changes in the reduction potential in the sediment surrounding the burrows did not influence the CO2 release from burrows. More oxidized conditions of plain sediment over time may explain the increase in CO2 release until the end of the wet season. CO2 released by U. cordatus and their burrows may be a significant pathway of CO2 export from mangrove sediments and should be considered in mangrove carbon budget estimates.

Thermal release of D2 from new Be-D co-deposits on previously baked co-deposits

Science.gov (United States)

Baldwin, M. J.; Doerner, R. P.

2015-12-01

Past experiments and modeling with the TMAP code in [1, 2] indicated that Be-D co-deposited layers are less (time-wise) efficiently desorbed of retained D in a fixed low-temperature bake, as the layer grows in thickness. In ITER, beryllium rich co-deposited layers will grow in thickness over the life of the machine. Although, compared with the analyses in [1, 2], ITER presents a slightly different bake efficiency problem because of instances of prior tritium recover/control baking. More relevant to ITER, is the thermal release from a new and saturated co-deposit layer in contact with a thickness of previously-baked, less-saturated, co-deposit. Experiments that examine the desorption of saturated co-deposited over-layers in contact with previously baked under-layers are reported and comparison is made to layers of the same combined thickness. Deposition temperatures of ∼323 K and ∼373 K are explored. It is found that an instance of prior bake leads to a subtle effect on the under-layer. The effect causes the thermal desorption of the new saturated over-layer to deviate from the prediction of the validated TMAP model in [2]. Instead of the D thermal release reflecting the combined thickness and levels of D saturation in the over and under layer, experiment differs in that, i) the desorption is a fractional superposition of desorption from the saturated over-layer, with ii) that of the combined over and under -layer thickness. The result is not easily modeled by TMAP without the incorporation of a thin BeO inter-layer which is confirmed experimentally on baked Be-D co-deposits using X-ray micro-analysis.

Thermal release of D_2 from new Be-D co-deposits on previously baked co-deposits

International Nuclear Information System (INIS)

Baldwin, M.J.; Doerner, R.P.

2015-01-01

Past experiments and modeling with the TMAP code in [1, 2] indicated that Be-D co-deposited layers are less (time-wise) efficiently desorbed of retained D in a fixed low-temperature bake, as the layer grows in thickness. In ITER, beryllium rich co-deposited layers will grow in thickness over the life of the machine. Although, compared with the analyses in [1, 2], ITER presents a slightly different bake efficiency problem because of instances of prior tritium recover/control baking. More relevant to ITER, is the thermal release from a new and saturated co-deposit layer in contact with a thickness of previously-baked, less-saturated, co-deposit. Experiments that examine the desorption of saturated co-deposited over-layers in contact with previously baked under-layers are reported and comparison is made to layers of the same combined thickness. Deposition temperatures of ∼323 K and ∼373 K are explored. It is found that an instance of prior bake leads to a subtle effect on the under-layer. The effect causes the thermal desorption of the new saturated over-layer to deviate from the prediction of the validated TMAP model in [2]. Instead of the D thermal release reflecting the combined thickness and levels of D saturation in the over and under layer, experiment differs in that, i) the desorption is a fractional superposition of desorption from the saturated over-layer, with ii) that of the combined over and under -layer thickness. The result is not easily modeled by TMAP without the incorporation of a thin BeO inter-layer which is confirmed experimentally on baked Be-D co-deposits using X-ray micro-analysis.

Effects of ocean acidification on the shells of four Mediterranean gastropod species near a CO2 seep.

Science.gov (United States)

Duquette, Ashley; McClintock, James B; Amsler, Charles D; Pérez-Huerta, Alberto; Milazzo, Marco; Hall-Spencer, Jason M

2017-11-30

Marine CO 2 seeps allow the study of the long-term effects of elevated pCO 2 (ocean acidification) on marine invertebrate biomineralization. We investigated the effects of ocean acidification on shell composition and structure in four ecologically important species of Mediterranean gastropods (two limpets, a top-shell snail, and a whelk). Individuals were sampled from three sites near a volcanic CO 2 seep off Vulcano Island, Italy. The three sites represented ambient (8.15pH), moderate (8.03pH) and low (7.73pH) seawater mean pH. Shell mineralogy, microstructure, and mechanical strength were examined in all four species. We found that the calcite/aragonite ratio could vary and increased significantly with reduced pH in shells of one of the two limpet species. Moreover, each of the four gastropods displayed reductions in either inner shell toughness or elasticity at the Low pH site. These results suggest that near-future ocean acidification could alter shell biomineralization and structure in these common gastropods. Copyright © 2017 Elsevier Ltd. All rights reserved.

Under-expanded jets and dispersion in supercritical CO_2 releases from a large-scale pipeline

International Nuclear Information System (INIS)

Guo, Xiaolu; Yan, Xingqing; Yu, Jianliang; Zhang, Yongchun; Chen, Shaoyun; Mahgerefteh, Haroun; Martynov, Sergey; Collard, Alexander; Proust, Christophe

2016-01-01

Highlights: • A large-scale full instrumented CO_2 test pipeline (258 m long, 233 mm id) has been developed. • The dynamic pressure evolutions near the orifice were recorded with differential pressure transducers. • The highly under-expanded jet flow structure in the near-field was studied in supercritical leakage. • The formation of the visible cloud, the distributions of temperature and concentration in the far-field were analysed. - Abstract: Long-distance CO_2 pipelines will be widely applied to transport captured CO_2 from fossil fuel fired power plants for subsequent sequestration. In the event of pipeline failure a large mass of the inventory may be discharged within a short time, this represents a significant hazard if leaks continue undetected. An important result of the risk assessment for a CO_2 pipeline is the safety distance. At present the lack of knowledge concerning near-field source terms and the far-field dispersion behavior of CO_2 leaking from pipelines can make the calculation of safety distances imprecise. Study of near-field source terms and dispersion behavior is therefore necessary and of paramount importance for assessing safety distances and the impact of CO_2 pipeline releases on the surrounding environment. In order to study CO_2 pipeline leakage, a large-scale pipeline set-up with a total length of 258 m and an internal diameter of 233 mm was constructed to study the near-field characteristics and dispersion behavior of supercritical CO_2 during sudden releases. The dynamic pressure near the orifice and CO_2 concentrations and temperatures within the downstream dispersion region were measured together with the pressures inside the pipeline. The under-expanded jet flow structure and phase transitions in the near-field were studied for supercritical CO_2 released though different orifice diameters (15 mm, 50 mm and Full Bore Rupture). The formation of the visible cloud, the distribution of cloud temperatures and CO_2

Calculations from the Hadley Centre: The ocean is rising even with stable CO2

International Nuclear Information System (INIS)

Groenaas, Sigbjoern

2000-01-01

The article presents calculations and forecasts for the atmospheric CO 2 level changes in the period of 2000 to 2350. Correlations between the levels and the average global temperature and the sea level are studied for the period of 1850 to 2200. The main conclusion is that the sea level will continue to rise for several hundred years even with a stable atmospheric CO 2 concentration in the next century due to the slow response of oceans to global warming

First estimates of the contribution of CaCO3 precipitation to the release of CO2 to the atmosphere during young sea ice growth

Science.gov (United States)

Geilfus, N.-X.; Carnat, G.; Dieckmann, G. S.; Halden, N.; Nehrke, G.; Papakyriakou, T.; Tison, J.-L.; Delille, B.

2013-01-01

report measurements of pH, total alkalinity, air-ice CO2 fluxes (chamber method), and CaCO3 content of frost flowers (FF) and thin landfast sea ice. As the temperature decreases, concentration of solutes in the brine skim increases. Along this gradual concentration process, some salts reach their solubility threshold and start precipitating. The precipitation of ikaite (CaCO3.6H2O) was confirmed in the FF and throughout the ice by Raman spectroscopy and X-ray analysis. The amount of ikaite precipitated was estimated to be 25 µmol kg-1 melted FF, in the FF and is shown to decrease from 19 to 15 µmol kg-1 melted ice in the upper part and at the bottom of the ice, respectively. CO2 release due to precipitation of CaCO3 is estimated to be 50 µmol kg-1 melted samples. The dissolved inorganic carbon (DIC) normalized to a salinity of 10 exhibits significant depletion in the upper layer of the ice and in the FF. This DIC loss is estimated to be 2069 µmol kg-1 melted sample and corresponds to a CO2 release from the ice to the atmosphere ranging from 20 to 40 mmol m-2 d-1. This estimate is consistent with flux measurements of air-ice CO2 exchange. Our measurements confirm previous laboratory findings that growing young sea ice acts as a source of CO2 to the atmosphere. CaCO3 precipitation during early ice growth appears to promote the release of CO2 to the atmosphere; however, its contribution to the overall release by newly formed ice is most likely minor.

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.

Deglacial upwelling, productivity and CO2 outgassing in the North Pacific Ocean

Science.gov (United States)

Gray, William R.; Rae, James W. B.; Wills, Robert C. J.; Shevenell, Amelia E.; Taylor, Ben; Burke, Andrea; Foster, Gavin L.; Lear, Caroline H.

2018-05-01

The interplay between ocean circulation and biological productivity affects atmospheric CO2 levels and marine oxygen concentrations. During the warming of the last deglaciation, the North Pacific experienced a peak in productivity and widespread hypoxia, with changes in circulation, iron supply and light limitation all proposed as potential drivers. Here we use the boron-isotope composition of planktic foraminifera from a sediment core in the western North Pacific to reconstruct pH and dissolved CO2 concentrations from 24,000 to 8,000 years ago. We find that the productivity peak during the Bølling-Allerød warm interval, 14,700 to 12,900 years ago, was associated with a decrease in near-surface pH and an increase in pCO2, and must therefore have been driven by increased supply of nutrient- and CO2-rich waters. In a climate model ensemble (PMIP3), the presence of large ice sheets over North America results in high rates of wind-driven upwelling within the subpolar North Pacific. We suggest that this process, combined with collapse of North Pacific Intermediate Water formation at the onset of the Bølling-Allerød, led to high rates of upwelling of water rich in nutrients and CO2, and supported the peak in productivity. The respiration of this organic matter, along with poor ventilation, probably caused the regional hypoxia. We suggest that CO2 outgassing from the North Pacific helped to maintain high atmospheric CO2 concentrations during the Bølling-Allerød and contributed to the deglacial CO2 rise.

CO2 release experiment in the shallow subsurface at the Brackenridge Field Laboratory and numerical modeling

Science.gov (United States)

Yang, C.; Romanak, K.; Hovorka, S.

2009-12-01

Soil gas monitoring is one cost-effective approach to detect CO2 leak at geological sequestration sites. Therefore understanding CO2 gas transport in soil zones is important for detection of CO2 leaks. A field experiment of a small CO2 release was conducted at the Brackenridge Field Laboratory, the University of Texas at Austin. The field site consists of one injection well, two sensor wells and one gas station well (Figure 1). The injection well was completed with a PVC pipe to a depth of 1.1 m below surface. CO2 sensors were deployed in sensor wells about 42 cm from the injection well at depths of 1.1 m having no subsurface PVC pipes but only a PVC protector cap at the surface. The gas monitoring station about 72 cm away from the injection well contains 3 copper tubes each set at different depths in sand pack isolated with bentonite clay. The CO2 release experiment started on March 4, 2009. A total 36.76 liters of CO2 were injected at 1 m depth at a rate of 100 ml/minute for 6 hours. Subsurface CO2 gas concentrations (before, during, and after the injection) were continuously monitored in sensor wells. Real-time CO2 concentrations were monitored at the gas station using an SRI 8610 gas chromatograph (GC) fitted with flame ionization detector (FID) and a thermal conductivity detector (TCD). A numerical model was constructed to simulate CO2 release experiments. The model takes into account CO2 diffusion and dissolution in pore water. Air in the pore space is assumed stagnant. Model domain consists of four soil layers and one atmospheric layer. The groundwater table is about 2.4 meters below ground surface. The model was calibrated with respect to diffusion coefficient (transport parameter) and the injection rate (mass parameter). Model results fit well with CO2 measurements at the sensor wells and the gas station. However, the calibrated injection rate underestimates measured injection rate.

Studies on CO2 removal and reduction. CO2 taisaku kenkyu no genjo

Energy Technology Data Exchange (ETDEWEB)

Shindo, Y [National Institute of Materials and Chemical Research, Tsukuba (Japan)

1993-02-01

This paper summarizes study trends mainly in CO2 fixing processes. Underground CO2 storage is a most promising method because it can fix a huge amount of CO2 and has low effects on ecological systems. Storing CO2 in ocean includes such methods as storing it in deep oceans; storing it in deep ocean beds; dissolving it into sea water; neutralizing it with calcium carbonates; and precipitating it as dry ice. Japan, disposing CO2 in these ways, may create international problems. Separation of CO2 may use a chemical absorption process as a superior method. Other processes discussed include a physical adsorption method and a membrane separation method. A useful method for CO2 fixation using marine organisms is fixation using coral reefs. This process will require an overall study including circulation of phosphorus and nitrogen. Marine organisms may include planktons and algae. CO2 fixation using land plants may be able to fix one trillion and 8 hundred billion tons of CO2 as converted to carbon. This process would require forest protection, prevention of desertification, and tree planting. Discussions are being given also on improving power generation cycles, recovering CO2 from automotive exhausts, and backfilling carbons into ground by means of photosynthesis. 23 refs., 7 figs., 1 tab.

Effect of ocean acidification on the benthic foraminifera

NARCIS (Netherlands)

Keul, N.; Langer, G.; de Nooijer, L.J.; Bijma, J.

2013-01-01

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

Acute physiological impacts of CO{sub 2} ocean sequestration on marine animals

Energy Technology Data Exchange (ETDEWEB)

Ishimatsu, A.; Hayashi, M.; Lee, K.S.; Murata, K.; Kumagai, E. [Nagasaki Univ., Nagasaki (Japan). Marine Research Inst.; Kikkawa, T. [Marine Ecology Research Inst., Chiba (Japan). Central Laboratory; Kita, J. [Research Inst. of Innovative Technology for the Earth, Kyoto (Japan)

2005-07-01

The biological impacts of ocean carbon dioxide (CO{sub 2}) sequestration must be carefully considered before it is implemented as a mitigation strategy. This paper presented details of a study investigating the effects of high CO{sub 2} concentrations on marine fish, lobster, and octopus. The influence of water temperature on the physiological effects of CO{sub 2} was also discussed. In the first part of the study, eggs and larvae of red seabream were exposed to both CO{sub 2} and HCI-acidified seawater at identical pH levels. Seabream in the CO{sub 2} group showed a much higher mortality rate than fish in the HCI group. Other tests showed that Japanese Flounder died after complete recovery of pH in seawater equilibrated with 5 per cent CO{sub 2}. Cardiac output was rapidly depressed in Yellowtail fish without significant changes in blood oxygen concentrations. Lower temperatures resulted in higher mortality and delayed pH recovery during hypercapnia in all fish. Western rock lobsters were the most tolerant to CO{sub 2} among all species tested. The recovery of hemolymph pH was complete at exposure to CO{sub 2} concentrations of 1 per cent. Changes in hemolymph bicarbonate concentrations indicated that acid-based regulatory mechanisms differed between fish and lobsters. Mortality rates for octopus were significant at CO{sub 2} concentrations of 1 per cent. The results of all tests showed that aquatic animals are more susceptible to increases in ambient CO{sub 2} levels than terrestrial animals. It was concluded that even slight elevations in CO{sub 2} concentration levels adversely affected physiological functioning in the tested species. It was concluded that CO{sub 2} sequestration in deeper, colder waters will have a more pronounced effect on aquatic animals due to the interactions between CO{sub 2} and lower temperatures, as well as the fact that most deep-sea fish are less tolerant to environmental perturbations. 3 refs., 1 tab., 3 figs.

Ocean Warming and CO2-Induced Acidification Impact the Lipid Content of a Marine Predatory Gastropod

Directory of Open Access Journals (Sweden)

Roselyn Valles-Regino

2015-09-01

Full Text Available Ocean warming and acidification are current global environmental challenges impacting aquatic organisms. A shift in conditions outside the optimal environmental range for marine species is likely to generate stress that could impact metabolic activity, with consequences for the biosynthesis of marine lipids. The aim of this study was to investigate differences in the lipid content of Dicathais orbita exposed to current and predicted future climate change scenarios. The whelks were exposed to a combination of temperature and CO2-induced acidification treatments in controlled flowthrough seawater mesocosms for 35 days. Under current conditions, D. orbita foot tissue has an average of 6 mg lipid/g tissue, but at predicted future ocean temperatures, the total lipid content dropped significantly, to almost half. The fatty acid composition is dominated by polyunsaturated fatty acids (PUFA 52% with an n-3:6 fatty acid ratio of almost 2, which remains unchanged under future ocean conditions. However, we detected an interactive effect of temperature and pCO2 on the % PUFAs and n-3 and n-6 fatty acids were significantly reduced by elevated water temperature, while both the saturated and monounsaturated fatty acids were significantly reduced under increased pCO2 acidifying conditions. The present study indicates the potential for relatively small predicted changes in ocean conditions to reduce lipid reserves and alter the fatty acid composition of a predatory marine mollusc. This has potential implications for the growth and survivorship of whelks under future conditions, but only minimal implications for human consumption of D. orbita as nutritional seafood are predicted.

Determining the age of CO2 Released From Mountain Birch Forest and Heath in Arctic Sweden

Science.gov (United States)

Hartley, I. P.; Garnett, M. H.; Hopkins, D. W.; Sommerkorn, M.; Wookey, P. A.

2008-12-01

Nuclear weapons testing released a large amount of 14C into the atmosphere during the mid 20th Century. This radiocarbon pulse provides a tracer that can be used to determine the age of C released from plants and soils. Such information is critical for predicting how terrestrial C storage will respond to global change. If respired CO2 is mainly modern, then respiration and photosynthesis are tightly coupled. In contrast, if older C is being mineralized then there is more potential for climate change to induce C loss. We carried out one of the first studies to measure seasonal variations in the 14C content of CO2 released from arctic ecosystems. Using molecular sieves, we trapped CO2 respired from a mountain birch forest and heath near Abisko, northern Sweden and measured 14C contents by accelerator mass spectrometry. CO2 was collected from both vegetated plots (control) and clipped and trenched plots (CT) on three occasions during the 2007 growing season. In addition, we used a new passive sampling technique to collect CO2 from the CT plots during winter 2007-2008. Assuming that the respired C was derived from post bomb sources (justifiable as the majority of each soil profile was enriched with bomb C), we estimated the age of the CO2 and how it changed during the year in response to changes in plant activity and key environmental drivers. On the heath, the mean age of the CO2 respired from the control plots increased from 4 to 6 years old during the growing season. The CO2 respired from the CT plots increased from 5 years old in early June to 11 years old by July, but then declined to 8 years old in September. The C released during winter was also 8 years old. In the Birch forest, the mean age of CO2 respired from the CT plots increased from 4 years old in late May to 8-9 years old during July and September. However, during winter, the CO2 released was >10 years old. In the control plots, the age of respired CO2 increased from being 1 year old in late May to 6

Measurements of the total CO2 concentration and partial pressure of CO2 in seawater during WOCE expeditions in the South Pacific Ocean

International Nuclear Information System (INIS)

Takahashi, T.; Goddard, J.G.; Chipman, D.W.; Rubin, S.I.

1993-01-01

During the first year of the grant, we participated in three WOCE expeditions (a total of 152 days at sea) in the South Pacific Ocean, and the field phase of the proposed investigation has been successfully completed. The total CO 2 concentration and pCO 2 were determined at sea in 4419 water samples collected at 422 stations. On the basis of the shipboard analyses of SIO Reference Solutions for CO, and a comparison with the results of previous expeditions, the overall precision of our total CO 2 determinations is estimated to be about ±2 uM/kg. The deep water data indicate that there is a CO 2 maximum centered about 2600 meters deep. This appears to represent a southward return flow from the North Pacific. The magnitude and distribution of the CO, maximum observed along the 135.0 degrees W meridian differ from those observed along the 150.5 degrees W meridian due to Tuamotu Archipelago, a topographic high which interferes with the southward return flow. The surface water pCO 2 data indicate that the South Pacific sub-tropical gyre water located between about 15 degrees S and 50 degrees S is a sink for atmospheric CO 2

Ocean Bottom Pressure Seasonal Cycles and Decadal Trends from GRACE Release-05: Ocean Circulation Implications

Science.gov (United States)

Johnson, G. C.; Chambers, D. P.

2013-12-01

Ocean mass variations are important for diagnosing sea level budgets, the hydrological cycle and global energy budget, as well as ocean circulation variability. Here seasonal cycles and decadal trends of ocean mass from January 2003 to December 2012, both global and regional, are analyzed using GRACE Release 05 data. The trend of global flux of mass into the ocean approaches 2 cm decade-1 in equivalent sea level rise. Regional trends are of similar magnitude, with the North Pacific, South Atlantic, and South Indian oceans generally gaining mass and other regions losing mass. These trends suggest a spin-down of the North Pacific western boundary current extension and the Antarctic Circumpolar Current in the South Atlantic and South Indian oceans. The global average seasonal cycle of ocean mass is about 1 cm in amplitude, with a maximum in early October and volume fluxes in and out of the ocean reaching 0.5 Sv (1 Sv = 1 × 106 m3 s-1) when integrated over the area analyzed here. Regional patterns of seasonal ocean mass change have typical amplitudes of 1-4 cm, and include maxima in the subtropics and minima in the subpolar regions in hemispheric winters. The subtropical mass gains and subpolar mass losses in the winter spin up both subtropical and subpolar gyres, hence the western boundary current extensions. Seasonal variations in these currents are order 10 Sv, but since the associated depth-averaged current variations are only order 0.1 cm s-1, they would be difficult to detect using in situ oceanographic instruments. a) Amplitude (colors, in cm) and b) phase (colors, in months of the year) of an annual harmonic fit to monthly GRACE Release 05 CSR 500 km smoothed maps (concurrently with a trend and the semiannual harmonic). The 97.5% confidence interval for difference from zero is also indicated (solid black line). Data within 300 km of coastlines are not considered.

Thermal release of D{sub 2} from new Be-D co-deposits on previously baked co-deposits

Energy Technology Data Exchange (ETDEWEB)

Baldwin, M.J., E-mail: m1baldwin@ucsd.edu; Doerner, R.P.

2015-12-15

Past experiments and modeling with the TMAP code in [1, 2] indicated that Be-D co-deposited layers are less (time-wise) efficiently desorbed of retained D in a fixed low-temperature bake, as the layer grows in thickness. In ITER, beryllium rich co-deposited layers will grow in thickness over the life of the machine. Although, compared with the analyses in [1, 2], ITER presents a slightly different bake efficiency problem because of instances of prior tritium recover/control baking. More relevant to ITER, is the thermal release from a new and saturated co-deposit layer in contact with a thickness of previously-baked, less-saturated, co-deposit. Experiments that examine the desorption of saturated co-deposited over-layers in contact with previously baked under-layers are reported and comparison is made to layers of the same combined thickness. Deposition temperatures of ∼323 K and ∼373 K are explored. It is found that an instance of prior bake leads to a subtle effect on the under-layer. The effect causes the thermal desorption of the new saturated over-layer to deviate from the prediction of the validated TMAP model in [2]. Instead of the D thermal release reflecting the combined thickness and levels of D saturation in the over and under layer, experiment differs in that, i) the desorption is a fractional superposition of desorption from the saturated over-layer, with ii) that of the combined over and under -layer thickness. The result is not easily modeled by TMAP without the incorporation of a thin BeO inter-layer which is confirmed experimentally on baked Be-D co-deposits using X-ray micro-analysis.

A joint global carbon inversion system using both CO2 and 13CO2 atmospheric concentration data

Science.gov (United States)

Chen, Jing M.; Mo, Gang; Deng, Feng

2017-03-01

Observations of 13CO2 at 73 sites compiled in the GLOBALVIEW database are used for an additional constraint in a global atmospheric inversion of the surface CO2 flux using CO2 observations at 210 sites (62 collocated with 13CO2 sites) for the 2002-2004 period for 39 land regions and 11 ocean regions. This constraint is implemented using prior CO2 fluxes estimated with a terrestrial ecosystem model and an ocean model. These models simulate 13CO2 discrimination rates of terrestrial photosynthesis and ocean-atmosphere diffusion processes. In both models, the 13CO2 disequilibrium between fluxes to and from the atmosphere is considered due to the historical change in atmospheric 13CO2 concentration. This joint inversion system using both13CO2 and CO2 observations is effectively a double deconvolution system with consideration of the spatial variations of isotopic discrimination and disequilibrium. Compared to the CO2-only inversion, this 13CO2 constraint on the inversion considerably reduces the total land carbon sink from 3.40 ± 0.84 to 2.53 ± 0.93 Pg C year-1 but increases the total oceanic carbon sink from 1.48 ± 0.40 to 2.36 ± 0.49 Pg C year-1. This constraint also changes the spatial distribution of the carbon sink. The largest sink increase occurs in the Amazon, while the largest source increases are in southern Africa, and Asia, where CO2 data are sparse. Through a case study, in which the spatial distribution of the annual 13CO2 discrimination rate over land is ignored by treating it as a constant at the global average of -14. 1 ‰, the spatial distribution of the inverted CO2 flux over land was found to be significantly modified (up to 15 % for some regions). The uncertainties in our disequilibrium flux estimation are 8.0 and 12.7 Pg C year-1 ‰ for land and ocean, respectively. These uncertainties induced the unpredictability of 0.47 and 0.54 Pg C year-1 in the inverted CO2 fluxes for land and ocean, respectively. Our joint inversion system is therefore

H2O and CO2 devolatilization in subduction zones: implications for the global water and carbon cycles (Invited)

Science.gov (United States)

van Keken, P. E.; Hacker, B. R.; Syracuse, E. M.; Abers, G. A.

2010-12-01

Subduction of sediments and altered oceanic crust functions as a major carbon sink. Upon subduction the carbon may be released by progressive metamorphic reactions, which can be strongly enhanced by free fluids. Quantification of the CO2 release from subducting slabs is important to determine the provenance of CO2 that is released by the volcanic arc and to constrain the flux of carbon to the deeper mantle. In recent work we used a global set of high resolution thermal models of subduction zones to predict the flux of H2O from the subducting slab (van Keken, Hacker, Syracuse, Abers, Subduction factory 4: Depth-dependent flux of H2O from subducting slabs worldwide, J. Geophys. Res., under review) which provides a new estimate of the dehydration efficiency of the global subducting system. It was found that mineralogically bound water can pass efficiently through old and fast subduction zones (such as in the western Pacific) but that warm subduction zones (such as Cascadia) see nearly complete dehydration of the subducting slab. The top of the slab is sufficiently hot in all subduction zones that the upper crust dehydrates significantly. The degree and depth of dehydration is highly diverse and strongly depends on (p,T) and bulk rock composition. On average about one third of subducted H2O reaches 240 km depth, carried principally and roughly equally in the gabbro and peridotite sections. The present-day global flux of H2O to the deep mantle translates to an addition of about one ocean mass over the age of the Earth. We extend the slab devolatilization work to carbon by providing an update to Gorman et al. (Geochem. Geophys. Geosyst, 2006), who quantified the effects of free fluids on CO2 release. The thermal conditions were based on three end-member subduction zones with linear interpolation to provide a global CO2 flux. We use the new high resolution and global set of models to provide higher resolution predictions for the provenance and pathways of CO2 release to

Sensitivity to ocean acidification parallels natural pCO2 gradients experienced by Arctic copepods under winter sea ice

Science.gov (United States)

Lewis, Ceri N.; Brown, Kristina A.; Edwards, Laura A.; Cooper, Glenn; Findlay, Helen S.

2013-01-01

The Arctic Ocean already experiences areas of low pH and high CO2, and it is expected to be most rapidly affected by future ocean acidification (OA). Copepods comprise the dominant Arctic zooplankton; hence, their responses to OA have important implications for Arctic ecosystems, yet there is little data on their current under-ice winter ecology on which to base future monitoring or make predictions about climate-induced change. Here, we report results from Arctic under-ice investigations of copepod natural distributions associated with late-winter carbonate chemistry environmental data and their response to manipulated pCO2 conditions (OA exposures). Our data reveal that species and life stage sensitivities to manipulated OA conditions were correlated with their vertical migration behavior and with their natural exposures to different pCO2 ranges. Vertically migrating adult Calanus spp. crossed a pCO2 range of >140 μatm daily and showed only minor responses to manipulated high CO2. Oithona similis, which remained in the surface waters and experienced a pCO2 range of <75 μatm, showed significantly reduced adult and nauplii survival in high CO2 experiments. These results support the relatively untested hypothesis that the natural range of pCO2 experienced by an organism determines its sensitivity to future OA and highlight that the globally important copepod species, Oithona spp., may be more sensitive to future high pCO2 conditions compared with the more widely studied larger copepods. PMID:24297880

A shallow subsurface controlled release facility in Bozeman, Montana, USA, for testing near surface CO2 detection techniques and transport models

Energy Technology Data Exchange (ETDEWEB)

Spangler, Lee H.; Dobeck, Laura M.; Repasky, Kevin S.; Nehrir, Amin R.; Humphries, Seth D.; Barr, Jamie L.; Keith, Charlie J.; Shaw, Joseph A.; Rouse, Joshua H.; Cunningham, Alfred B.; Benson, Sally M.; Oldenburg, Curtis M.; Lewicki, Jennifer L.; Wells, Arthur W.; Diehl, J. R.; Strazisar, Brian; Fessenden, Julianna; Rahn, Thom A.; Amonette, James E.; Barr, Jonathan L.; Pickles, William L.; Jacobson, James D.; Silver, Eli A.; Male, Erin J.; Rauch, Henry W.; Gullickson, Kadie; Trautz, Robert; Kharaka, Yousif; Birkholzer, Jens; Wielopolski, Lucien

2010-03-01

A facility has been constructed to perform controlled shallow releases of CO2 at flow rates that challenge near surface detection techniques and can be scalable to desired retention rates of large scale CO2 storage projects. Preinjection measurements were made to determine background conditions and characterize natural variability at the site. Modeling of CO2 transport and concentration in saturated soil and the vadose zone was also performed to inform decisions about CO2 release rates and sampling strategies. Four releases of CO2 were carried out over the summer field seasons of 2007 and 2008. Transport of CO2 through soil, water, plants, and air was studied using near surface detection techniques. Soil CO2 flux, soil gas concentration, total carbon in soil, water chemistry, plant health, net CO2 flux, atmospheric CO2 concentration, movement of tracers, and stable isotope ratios were among the quantities measured. Even at relatively low fluxes, most techniques were able to detect elevated levels of CO2 in the soil, atmosphere, or water. Plant stress induced by CO2 was detectable above natural seasonal variations.

Modeling of Oceanic Gas Hydrate Instability and Methane Release in Response to Climate Change

Energy Technology Data Exchange (ETDEWEB)

Reagan, Matthew; Reagan, Matthew T.; Moridis, George J.

2008-04-15

Paleooceanographic evidence has been used to postulate that methane from oceanic hydrates may have had a significant role in regulating global climate, implicating global oceanic deposits of methane gas hydrate as the main culprit in instances of rapid climate change that have occurred in the past. However, the behavior of contemporary oceanic methane hydrate deposits subjected to rapid temperature changes, like those predicted under future climate change scenarios, is poorly understood. To determine the fate of the carbon stored in these hydrates, we performed simulations of oceanic gas hydrate accumulations subjected to temperature changes at the seafloor and assessed the potential for methane release into the ocean. Our modeling analysis considered the properties of benthic sediments, the saturation and distribution of the hydrates, the ocean depth, the initial seafloor temperature, and for the first time, estimated the effect of benthic biogeochemical activity. The results show that shallow deposits--such as those found in arctic regions or in the Gulf of Mexico--can undergo rapid dissociation and produce significant methane fluxes of 2 to 13 mol/yr/m{sup 2} over a period of decades, and release up to 1,100 mol of methane per m{sup 2} of seafloor in a century. These fluxes may exceed the ability of the seafloor environment (via anaerobic oxidation of methane) to consume the released methane or sequester the carbon. These results will provide a source term to regional or global climate models in order to assess the coupling of gas hydrate deposits to changes in the global climate.

Modelling of oceanic gas hydrate instability and methane release in response to climate change

International Nuclear Information System (INIS)

Reagan, M.T.; Moridis, G.J.

2008-01-01

Methane releases from oceanic hydrates are thought to have played a significant role in climatic changes that have occurred in the past. In this study, gas hydrate accumulations subjected to temperature changes were modelled in order to assess their potential for future methane releases into the ocean. Recent ocean and atmospheric chemistry studies were used to model 2 climate scenarios. Two types of hydrate accumulations were used to represent dispersed, low-saturation deposits. The 1-D multiphase thermodynamic-hydrological model considered the properties of benthic sediments; ocean depth; sea floor temperature; the saturation and distribution of the hydrates; and the effect of benthic biogeochemical activity. Results of the simulations showed that shallow deposits undergo rapid dissociation and are capable of producing methane fluxes of 2 to 13 mol m 3 per year over a period of decades. The fluxes exceed the ability of the anaerobic sea floor environment to sequester or consume the methane. A large proportion of the methane released in the scenarios emerged in the gas phase. Arctic hydrates may pose a threat to regional and global ecological systems. It was concluded that results of the study will be coupled with global climate models in order to assess the impact of the methane releases in relation to global climatic change. 39 refs., 5 figs

TMAP-7 simulation of D2 thermal release data from Be co-deposited layers

International Nuclear Information System (INIS)

Baldwin, M.J.; Schwarz-Selinger, T.; Yu, J.H.; Doerner, R.P.

2013-01-01

The efficacy of (1) bake-out at 513 K and 623 K, and (2) thermal transient (10 ms) loading to up to 1000 K, is explored for reducing D inventory in 1 μm thick Be–D (D/Be ∼0.1) co-deposited layers formed at 323 K for experiment (1) and ∼500 K for experiment (2). D release data from co-deposits are obtained by thermal desorption and used to validate a model input into the Tritium Migration and Analysis Program 7 (TMAP). In (1), good agreement with experiment is found for a TMAP model encorporating traps of activation energies, 0.80 eV and 0.98 eV, whereas an additional 2 eV trap was required to model experiment (2). Thermal release is found to be trap limited, but simulations are optimal when surface recombination is taken into account. Results suggest that thick built-up co-deposited layers will hinder ITER inventory control, and that bake periods (∼1 day) will be more effective in inventory reduction than transient thermal loading

TMAP-7 simulation of D2 thermal release data from Be co-deposited layers

Science.gov (United States)

Baldwin, M. J.; Schwarz-Selinger, T.; Yu, J. H.; Doerner, R. P.

2013-07-01

The efficacy of (1) bake-out at 513 K and 623 K, and (2) thermal transient (10 ms) loading to up to 1000 K, is explored for reducing D inventory in 1 μm thick Be-D (D/Be ˜0.1) co-deposited layers formed at 323 K for experiment (1) and ˜500 K for experiment (2). D release data from co-deposits are obtained by thermal desorption and used to validate a model input into the Tritium Migration & Analysis Program 7 (TMAP). In (1), good agreement with experiment is found for a TMAP model encorporating traps of activation energies, 0.80 eV and 0.98 eV, whereas an additional 2 eV trap was required to model experiment (2). Thermal release is found to be trap limited, but simulations are optimal when surface recombination is taken into account. Results suggest that thick built-up co-deposited layers will hinder ITER inventory control, and that bake periods (˜1 day) will be more effective in inventory reduction than transient thermal loading.

Low pCO2 under sea-ice melt in the Canada Basin of the western Arctic Ocean

Science.gov (United States)

Kosugi, Naohiro; Sasano, Daisuke; Ishii, Masao; Nishino, Shigeto; Uchida, Hiroshi; Yoshikawa-Inoue, Hisayuki

2017-12-01

In September 2013, we observed an expanse of surface water with low CO2 partial pressure (pCO2sea) (Ocean. The large undersaturation of CO2 in this region was the result of massive primary production after the sea-ice retreat in June and July. In the surface of the Canada Basin, salinity was low ( 20 µmol kg-1) in the subsurface low pCO2sea layer in the Canada Basin indicated significant net primary production undersea and/or in preformed condition. If these low pCO2sea layers surface by wind mixing, they will act as additional CO2 sinks; however, this is unlikely because intensification of stratification by sea-ice melt inhibits mixing across the halocline.

FY 2000 report on the results of the R and D of the prediction technology for environmental effects of CO2 ocean sequestration. Ocean survey and development of the assessment technology for capacity of CO2 sequestration; 2000 nendo nisanka tanso no kaiyo kakuri ni tomonau kankyo eikyo yosoku gijutsu kenkyu kaihatsu seika hokokusho. Kaiyo chosa oyobi CO2 kakuri noryoku hyoka gijutsu no kaihatsu

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-03-01

Assuming the dissolution/sequestration of CO2 at the medium-depth sea area around Japan (depth: 1,000-2,000m), the development was being proceeded with of the assessment technology for capacity of CO2 ocean sequestration and the prediction technology of environmental effects at the point of CO2 discharge. In FY 2000, conducted were the ocean survey and the development of assessment technology for CO2 sequestration capacity. In the investigational study, the following three were carried out: 1) survey/observation of the flow field on the line of 165 degrees of east longitude, and acquisition of various data such as the distribution of carbonic acid base substances and the speed of carbon transport; 2) study of the amount of existence of organisms and kind/composition of the medium-depth plankton at the typical observation points; 3) test/experiment actually conducted in the sea area for the experimental equipment for CaCO3 dissolution experimental equipment for studying interactions between the CO2 and CaCO3 dissolved into the medium-depth sea. As to the development of the assessment technology, carried out were the heightening of accuracy of medium-depth ocean circulation models using the inverse method already developed and the estimation of the flow field using the observation data. At the same time, the estimation of the flow field, etc. were conducted using large circulation ocean models. (NEDO)

Evaluating Potential for Large Releases from CO2 Storage Reservoirs: Analogs, Scenarios, and Modeling Needs

International Nuclear Information System (INIS)

Birkholzer, Jens; Pruess, Karsten; Lewicki, Jennifer; Tsang, Chin-Fu; Karimjee, Anhar

2005-01-01

While the purpose of geologic storage of CO 2 in deep saline formations is to trap greenhouse gases underground, the potential exists for CO 2 to escape from the target reservoir, migrate upward along permeable pathways, and discharge at the land surface. Such discharge is not necessarily a serious concern, as CO 2 is a naturally abundant and relatively benign gas in low concentrations. However, there is a potential risk to health, safety and environment (HSE) in the event that large localized fluxes of CO 2 were to occur at the land surface, especially where CO 2 could accumulate. In this paper, we develop possible scenarios for large CO 2 fluxes based on the analysis of natural analogues, where large releases of gas have been observed. We are particularly interested in scenarios which could generate sudden, possibly self-enhancing, or even eruptive release events. The probability for such events may be low, but the circumstances under which they might occur and potential consequences need to be evaluated in order to design appropriate site selection and risk management strategies. Numerical modeling of hypothetical test cases is needed to determine critical conditions for such events, to evaluate whether such conditions may be possible at designated storage sites, and, if applicable, to evaluate the potential HSE impacts of such events and design appropriate mitigation strategies

Oysters and eelgrass: potential partners in a high pCO2 ocean.

Science.gov (United States)

Groner, Maya L; Burge, Colleen A; Cox, Ruth; Rivlin, Natalie; Turner, Mo; Van Alstyne, Kathryn L; Wyllie-Echeverria, Sandy; Bucci, John; Staudigel, Philip; Friedman, Carolyn S

2018-05-25

Climate change is affecting the health and physiology of marine organisms and altering species interactions. Ocean acidification (OA) threatens calcifying organisms such as the Pacific oyster, Crassostrea gigas. In contrast, seagrasses, such as the eelgrass Zostera marina, can benefit from the increase in available carbon for photosynthesis found at a lower seawater pH. Seagrasses can remove dissolved inorganic carbon from OA environments, creating local daytime pH refugia. Pacific oysters may improve the health of eelgrass by filtering out pathogens such as Labyrinthula zosterae (LZ), which causes eelgrass wasting disease (EWD). We examined how co-culture of eelgrass ramets and juvenile oysters affected the health and growth of eelgrass and the mass of oysters under different pCO 2 exposures. In Phase I, each species was cultured alone or in co-culture at 12°C across ambient, medium, and high pCO 2 conditions, (656, 1158 and1606 μatm pCO 2 , respectively). Under high pCO 2 , eelgrass grew faster and had less severe EWD (contracted in the field prior to the experiment). Co-culture with oysters also reduced the severity of EWD. While the presence of eelgrass decreased daytime pCO 2 , this reduction was not substantial enough to ameliorate the negative impact of high pCO 2 on oyster mass. In Phase II, eelgrass alone or oysters and eelgrass in co-culture were held at 15°C under ambient and high pCO 2 conditions, (488 and 2013 μatm pCO 2 , respectively). Half of the replicates were challenged with cultured LZ. Concentrations of defensive compounds in eelgrass (total phenolics and tannins), were altered by LZ exposure and pCO 2 treatments. Greater pathogen loads and increased EWD severity were detected in LZ exposed eelgrass ramets; EWD severity was reduced at high relative to low pCO 2 . Oyster presence did not influence pathogen load or EWD severity; high LZ concentrations in experimental treatments may have masked the effect of this treatment. Collectively, these

Seaweed fails to prevent ocean acidification impact on foraminifera along a shallow-water CO2 gradient.

Science.gov (United States)

Pettit, Laura R; Smart, Christopher W; Hart, Malcolm B; Milazzo, Marco; Hall-Spencer, Jason M

2015-05-01

Ocean acidification causes biodiversity loss, alters ecosystems, and may impact food security, as shells of small organisms dissolve easily in corrosive waters. There is a suggestion that photosynthetic organisms could mitigate ocean acidification on a local scale, through seagrass protection or seaweed cultivation, as net ecosystem organic production raises the saturation state of calcium carbonate making seawater less corrosive. Here, we used a natural gradient in calcium carbonate saturation, caused by shallow-water CO2 seeps in the Mediterranean Sea, to assess whether seaweed that is resistant to acidification (Padina pavonica) could prevent adverse effects of acidification on epiphytic foraminifera. We found a reduction in the number of species of foraminifera as calcium carbonate saturation state fell and that the assemblage shifted from one dominated by calcareous species at reference sites (pH ∼8.19) to one dominated by agglutinated foraminifera at elevated levels of CO2 (pH ∼7.71). It is expected that ocean acidification will result in changes in foraminiferal assemblage composition and agglutinated forms may become more prevalent. Although Padina did not prevent adverse effects of ocean acidification, high biomass stands of seagrass or seaweed farms might be more successful in protecting epiphytic foraminifera.

Concentrations and (delta)13C values of atmospheric CO2 from oceanic atmosphere through time: polluted and non-polluted areas

International Nuclear Information System (INIS)

Longinelli, Antonio; Selmo, Enrico; Lenaz, Renzo; Ori, Carlo

2005-01-01

CO 2 is one of the primary agents of global climate changes. The increase of atmospheric CO 2 concentration is essentially related to human-induced emissions and, particularly, to the burning of fossil fuel whose (delta) 13 C values are quite negative. Consequently, an increase of the CO 2 concentration in the atmosphere should be paralleled by a decrease of its (delta) 13 C. Continuous and/or spot measurements of CO 2 concentrations were repeatedly carried out during the last decade and in the same period of the year along hemispheric courses from Italy to Antarctica on a vessel of the Italian National Research Program in Antarctica. During these expeditions, discrete air samples were also collected in 4-l Pyrex flasks in order to carry out precise carbon isotope analyses on atmospheric CO 2 from different areas, including theoretically 'clean' open ocean areas, with the main purpose of comparing these open ocean results with the results obtained by the National Oceanic and Atmospheric Administration/World Meteorological Organization (NOAA/WMO) at land-based stations. According to the data obtained for these two variables, a relatively large atmospheric pollution is apparent in the Mediterranean area where the CO 2 concentration has reached the value of 384 ppmv while quite negative (delta) 13 C values have been measured only occasionally. In this area, southerly winds probably help to reduce the effect of atmospheric pollution even though, despite a large variability of CO 2 concentrations, these values are consistently higher than those measured in open ocean areas by a few ppmv to about 10 ppmv. A marked, though non-continuous, pollution is apparent in the area of the Bab-el-Mandeb strait where (delta) 13 C values considerably more negative than in the Central and Southern Red Sea were measured. The concentration of atmospheric CO 2 over the Central Indian Ocean increased from about 361 ppmv at the end of 1996 to about 373 ppmv at the end of 2003 (mean growth

Abiotic and seasonal control of soil-produced CO2 efflux in karstic ecosystems located in Oceanic and Mediterranean climates

Science.gov (United States)

Garcia-Anton, Elena; Cuezva, Soledad; Fernandez-Cortes, Angel; Alvarez-Gallego, Miriam; Pla, Concepcion; Benavente, David; Cañaveras, Juan Carlos; Sanchez-Moral, Sergio

2017-09-01

This study characterizes the processes involved in seasonal CO2 exchange between soils and shallow underground systems and explores the contribution of the different biotic and abiotic sources as a function of changing weather conditions. We spatially and temporally investigated five karstic caves across the Iberian Peninsula, which presented different microclimatic, geologic and geomorphologic features. The locations present Mediterranean and Oceanic climates. Spot air sampling of CO2 (g) and δ13CO2 in the caves, soils and outside atmospheric air was periodically conducted. The isotopic ratio of the source contribution enhancing the CO2 concentration was calculated using the Keeling model. We compared the isotopic ratio of the source in the soil (δ13Cs-soil) with that in the soil-underground system (δ13Cs-system). Although the studied field sites have different features, we found common seasonal trends in their values, which suggests a climatic control over the soil air CO2 and the δ13CO2 of the sources of CO2 in the soil (δ13Cs-soil) and the system (δ13Cs-system). The roots respiration and soil organic matter degradation are the main source of CO2 in underground environments, and the inlet of the gas is mainly driven by diffusion and advection. Drier and warmer conditions enhance soil-exterior CO2 interchange, reducing the CO2 concentration and increasing the δ13CO2 of the soil air. Moreover, the isotopic ratio of the source of CO2 in both the soil and the system tends to heavier values throughout the dry and warm season. We conclude that seasonal variations of soil CO2 concentration and its 13C/12C isotopic ratio are mainly regulated by thermo-hygrometric conditions. In cold and wet seasons, the increase of soil moisture reduces soil diffusivity and allows the storage of CO2 in the subsoil. During dry and warm seasons, the evaporation of soil water favours diffusive and advective transport of soil-derived CO2 to the atmosphere. The soil CO2 diffusion is

Acid-base physiology, neurobiology and behaviour in relation to CO2-induced ocean acidification.

Science.gov (United States)

Tresguerres, Martin; Hamilton, Trevor J

2017-06-15

Experimental exposure to ocean and freshwater acidification affects the behaviour of multiple aquatic organisms in laboratory tests. One proposed cause involves an imbalance in plasma chloride and bicarbonate ion concentrations as a result of acid-base regulation, causing the reversal of ionic fluxes through GABA A receptors, which leads to altered neuronal function. This model is exclusively based on differential effects of the GABA A receptor antagonist gabazine on control animals and those exposed to elevated CO 2 However, direct measurements of actual chloride and bicarbonate concentrations in neurons and their extracellular fluids and of GABA A receptor properties in aquatic organisms are largely lacking. Similarly, very little is known about potential compensatory mechanisms, and about alternative mechanisms that might lead to ocean acidification-induced behavioural changes. This article reviews the current knowledge on acid-base physiology, neurobiology, pharmacology and behaviour in relation to marine CO 2 -induced acidification, and identifies important topics for future research that will help us to understand the potential effects of predicted levels of aquatic acidification on organisms. © 2017. Published by The Company of Biologists Ltd.

Ocean acidification of a coastal Antarctic marine microbial community reveals a critical threshold for CO2 tolerance in phytoplankton productivity

Science.gov (United States)

Deppeler, Stacy; Petrou, Katherina; Schulz, Kai G.; Westwood, Karen; Pearce, Imojen; McKinlay, John; Davidson, Andrew

2018-01-01

High-latitude oceans are anticipated to be some of the first regions affected by ocean acidification. Despite this, the effect of ocean acidification on natural communities of Antarctic marine microbes is still not well understood. In this study we exposed an early spring, coastal marine microbial community in Prydz Bay to CO2 levels ranging from ambient (343 µatm) to 1641 µatm in six 650 L minicosms. Productivity assays were performed to identify whether a CO2 threshold existed that led to a change in primary productivity, bacterial productivity, and the accumulation of chlorophyll a (Chl a) and particulate organic matter (POM) in the minicosms. In addition, photophysiological measurements were performed to identify possible mechanisms driving changes in the phytoplankton community. A critical threshold for tolerance to ocean acidification was identified in the phytoplankton community between 953 and 1140 µatm. CO2 levels ≥ 1140 µatm negatively affected photosynthetic performance and Chl a-normalised primary productivity (csGPP14C), causing significant reductions in gross primary production (GPP14C), Chl a accumulation, nutrient uptake, and POM production. However, there was no effect of CO2 on C : N ratios. Over time, the phytoplankton community acclimated to high CO2 conditions, showing a down-regulation of carbon concentrating mechanisms (CCMs) and likely adjusting other intracellular processes. Bacterial abundance initially increased in CO2 treatments ≥ 953 µatm (days 3-5), yet gross bacterial production (GBP14C) remained unchanged and cell-specific bacterial productivity (csBP14C) was reduced. Towards the end of the experiment, GBP14C and csBP14C markedly increased across all treatments regardless of CO2 availability. This coincided with increased organic matter availability (POC and PON) combined with improved efficiency of carbon uptake. Changes in phytoplankton community production could have negative effects on the Antarctic food web and the

Ocean acidification of a coastal Antarctic marine microbial community reveals a critical threshold for CO2 tolerance in phytoplankton productivity

Directory of Open Access Journals (Sweden)

S. Deppeler

2018-01-01

Full Text Available High-latitude oceans are anticipated to be some of the first regions affected by ocean acidification. Despite this, the effect of ocean acidification on natural communities of Antarctic marine microbes is still not well understood. In this study we exposed an early spring, coastal marine microbial community in Prydz Bay to CO2 levels ranging from ambient (343 µatm to 1641 µatm in six 650 L minicosms. Productivity assays were performed to identify whether a CO2 threshold existed that led to a change in primary productivity, bacterial productivity, and the accumulation of chlorophyll a (Chl a and particulate organic matter (POM in the minicosms. In addition, photophysiological measurements were performed to identify possible mechanisms driving changes in the phytoplankton community. A critical threshold for tolerance to ocean acidification was identified in the phytoplankton community between 953 and 1140 µatm. CO2 levels  ≥ 1140 µatm negatively affected photosynthetic performance and Chl a-normalised primary productivity (csGPP14C, causing significant reductions in gross primary production (GPP14C, Chl a accumulation, nutrient uptake, and POM production. However, there was no effect of CO2 on C : N ratios. Over time, the phytoplankton community acclimated to high CO2 conditions, showing a down-regulation of carbon concentrating mechanisms (CCMs and likely adjusting other intracellular processes. Bacterial abundance initially increased in CO2 treatments  ≥ 953 µatm (days 3–5, yet gross bacterial production (GBP14C remained unchanged and cell-specific bacterial productivity (csBP14C was reduced. Towards the end of the experiment, GBP14C and csBP14C markedly increased across all treatments regardless of CO2 availability. This coincided with increased organic matter availability (POC and PON combined with improved efficiency of carbon uptake. Changes in phytoplankton community production could have negative

Calcification in Caribbean reef-building corals at high pCO2 levels in a recirculating ocean acidification exposure system

Science.gov (United States)

Projected increases in ocean pCO2 levels are anticipated to affect calcifying organisms more rapidly and to a greater extent than other marine organisms. The effects of ocean acidification (OA) have been documented in numerous species of corals in laboratory studies, largely test...

History of CO/sub 2/

Energy Technology Data Exchange (ETDEWEB)

Degens, E T

1979-01-01

Upon arrival on earth, the reduced carbon pool split into a series of compartments: core, mantle, crust, hydrosphere, atmosphere, and biosphere. This distribution pattern is caused by the ability of carbon to adjust structurally to a wide range of pressure and temperature, and to form simple and complex molecules with oxygen, hydrogen and nitrogen. Transformation also involved oxidation of carbon to CO/sub 2/ which is mediated at depth by minerals, such as magnetite, and by water vapor above critical temperature. Guided by mineral-organic interactions, simple carbon compounds evolved in near surface environments towards physiologically interesting biochemicals. Life, as an autocatalytic system, is considered an outgrowth of such a development. This article discusses environmental parameters that control the CO/sub 2/ system, past and present. Mantle and crustal evolution is the dynamo recharging the CO/sub 2/ in sea and air; the present rate of CO/sub 2/ release from the magma is 0.05 x 10/sup 15/ g C per year. Due to the enormous buffer capacity of the chemical system ocean, such rates are too small to seriously effect the level of CO/sub 2/ in our atmosphere. In the light of geological field data and stable isotope work, it is concluded that the CO/sub 2/ content in the atmosphere has remained fairly uniform since early Precambrian time; CO/sub 2/ should thus have had little impact on paleoclimate. In contrast, the massive discharge of man-made CO/sub 2/ into our atmosphere may have serious consequences for climate, environment and society in the years to come.

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.

Geoengineering impact of open ocean dissolution of olivine on atmospheric CO2, surface ocean pH and marine biology

International Nuclear Information System (INIS)

Köhler, Peter; Abrams, Jesse F; Völker, Christoph; Hauck, Judith; Wolf-Gladrow, Dieter A

2013-01-01

Ongoing global warming induced by anthropogenic emissions has opened the debate as to whether geoengineering is a ‘quick fix’ option. Here we analyse the intended and unintended effects of one specific geoengineering approach, which is enhanced weathering via the open ocean dissolution of the silicate-containing mineral olivine. This approach would not only reduce atmospheric CO 2 and oppose surface ocean acidification, but would also impact on marine biology. If dissolved in the surface ocean, olivine sequesters 0.28 g carbon per g of olivine dissolved, similar to land-based enhanced weathering. Silicic acid input, a byproduct of the olivine dissolution, alters marine biology because silicate is in certain areas the limiting nutrient for diatoms. As a consequence, our model predicts a shift in phytoplankton species composition towards diatoms, altering the biological carbon pumps. Enhanced olivine dissolution, both on land and in the ocean, therefore needs to be considered as ocean fertilization. From dissolution kinetics we calculate that only olivine particles with a grain size of the order of 1 μm sink slowly enough to enable a nearly complete dissolution. The energy consumption for grinding to this small size might reduce the carbon sequestration efficiency by ∼30%. (letter)

Co-ordination Action on Ocean Energy (CA-OE)

DEFF Research Database (Denmark)

Tedd, James; Frigaard, Peter

In October 2004, the Co-ordination Action on Ocean Energy (CA-OE) was launched, co-financed by the European Commission, under the Renewable Energy Technologies priority within the 6th Framework programme, contract number 502701, chaired by Kim Nielsen, Rambøll, Denmark. The project involves 41...... partners. In general the public is not aware of the development of ocean energy and its exploitation. There is a need to make a united effort from the developers and research community to present the various principles and results in a coordinated manner with public appeal. The main objectives of the Co......-ordination Action on Ocean Energy are: To develop a common knowledge base necessary for coherent research and development policiesTo bring a co-ordinated approach within key areas of ocean energy research and development.To provide a forum for the longer term marketing of promising research developments...

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

A Stratification Boomerang: Nonlinear Dependence of Deep Southern Ocean Ventilation on PCO2

Science.gov (United States)

Galbraith, E. D.; Merlis, T. M.

2014-12-01

Strong correlations between atmospheric CO2, Antarctic temperatures, and marine proxy records have hinted that ventilation of the deep Southern Ocean may have played a central role in the variations of CO2 over glacial-interglacial cycles. One proposition is that, in general, the Southern Ocean ventilates the deep more strongly under higher CO2, due to a change in winds and/or the dominance of thermal stratification in a warm ocean, which weakens ocean biological carbon storage. Here, we explore this idea with a suite of multi-millennial simulations using the GFDL CM2Mc global coupled model. The results are, indeed, consistent with increasing ventilation of the Southern Ocean as pCO2 increases above modern. However, they reveal a surprising twist under low pCO2: increased salinity of the Southern Ocean, due in part to weakening atmospheric moisture transport, actually increases ventilation rate of the deep ocean under low pCO2 as well. This implies that a nadir of Southern Ocean ventilation occurs at intermediate pCO2, which the model estimates as being close to that of the present-day. This is at odds with the interpretation that weak ventilation of the deep Southern Ocean was the unifying coupled mechanism for the glacial pCO2 cycles. Rather, it suggests that factors other than the ventilation rate of the deep Southern Ocean, such as iron fertilization, ecosystem changes, water mass distributions, and sea ice cover, were key players in the glacial-interglacial CO2 changes.

Gas hydrate dissociation prolongs acidification of the Anthropocene oceans

NARCIS (Netherlands)

Boudreau, B.P.; Luo, Yiming; Meysman, Filip J R; Middelburg, J.J.; Dickens, G.R.

2015-01-01

Anthropogenic warming of the oceans can release methane (CH4) currently stored in sediments as gas hydrates. This CH4 will be oxidized to CO2, thus increasing the acidification of the oceans. We employ a biogeochemical model of the multimillennial carbon cycle to determine the evolution of the

Application of a nonparametric approach to analyze delta-pCO2 data from the Southern Ocean

CSIR Research Space (South Africa)

Pretorius, WB

2011-11-01

Full Text Available NONPARAMETRIC APPROACH TO ANALYZE ?pCO2 DATA FROM THE SOUTHERN OCEAN Wesley B. Pretorius*1, Sonali Das2 and Paul J. Mostert1 *1 Cell: 0722897595, Department of Statistics and Actuarial Science, University of Stellenbosch, Private Bag X1, Matieland 7602...(9-10):1601-1622. Tans, P.P., Fung, I. Y. & Takahashi, T. 1990 Observational constraints on the global atmospheric CO2-budget. Science, 247:1431-1438. Telszewski, M., Chazottes, A., Schuster, U., Watson, A.J., Moulin, C., Bakker, D.C.E., Gonzalez-Davila, M...

TMAP-7 simulation of D{sub 2} thermal release data from Be co-deposited layers

Energy Technology Data Exchange (ETDEWEB)

Baldwin, M.J., E-mail: mbaldwin@ferp.ucsd.edu [Center for Energy Research, University of California at San Diego, La Jolla, CA 92093-0417 (United States); Schwarz-Selinger, T. [Max-Planck-Institut für Plasmaphysik, EURATOM Association, Boltzmannstrasse 2, 85748 Garching (Germany); Yu, J.H. [Center for Energy Research, University of California at San Diego, La Jolla, CA 92093-0417 (United States); Doerner, R.P., E-mail: rdoerner@ucsd.edu [Center for Energy Research, University of California at San Diego, La Jolla, CA 92093-0417 (United States)

2013-07-15

The efficacy of (1) bake-out at 513 K and 623 K, and (2) thermal transient (10 ms) loading to up to 1000 K, is explored for reducing D inventory in 1 μm thick Be–D (D/Be ∼0.1) co-deposited layers formed at 323 K for experiment (1) and ∼500 K for experiment (2). D release data from co-deposits are obtained by thermal desorption and used to validate a model input into the Tritium Migration and Analysis Program 7 (TMAP). In (1), good agreement with experiment is found for a TMAP model encorporating traps of activation energies, 0.80 eV and 0.98 eV, whereas an additional 2 eV trap was required to model experiment (2). Thermal release is found to be trap limited, but simulations are optimal when surface recombination is taken into account. Results suggest that thick built-up co-deposited layers will hinder ITER inventory control, and that bake periods (∼1 day) will be more effective in inventory reduction than transient thermal loading.

Seagrass habitat metabolism increases short-term extremes and long-term offset of CO2 under future ocean acidification.

Science.gov (United States)

Pacella, Stephen R; Brown, Cheryl A; Waldbusser, George G; Labiosa, Rochelle G; Hales, Burke

2018-04-10

The role of rising atmospheric CO 2 in modulating estuarine carbonate system dynamics remains poorly characterized, likely due to myriad processes driving the complex chemistry in these habitats. We reconstructed the full carbonate system of an estuarine seagrass habitat for a summer period of 2.5 months utilizing a combination of time-series observations and mechanistic modeling, and quantified the roles of aerobic metabolism, mixing, and gas exchange in the observed dynamics. The anthropogenic CO 2 burden in the habitat was estimated for the years 1765-2100 to quantify changes in observed high-frequency carbonate chemistry dynamics. The addition of anthropogenic CO 2 alters the thermodynamic buffer factors (e.g., the Revelle factor) of the carbonate system, decreasing the seagrass habitat's ability to buffer natural carbonate system fluctuations. As a result, the most harmful carbonate system indices for many estuarine organisms [minimum pH T , minimum Ω arag , and maximum pCO 2(s.w.) ] change up to 1.8×, 2.3×, and 1.5× more rapidly than the medians for each parameter, respectively. In this system, the relative benefits of the seagrass habitat in locally mitigating ocean acidification increase with the higher atmospheric CO 2 levels predicted toward 2100. Presently, however, these mitigating effects are mixed due to intense diel cycling of CO 2 driven by aerobic metabolism. This study provides estimates of how high-frequency pH T , Ω arag , and pCO 2(s.w.) dynamics are altered by rising atmospheric CO 2 in an estuarine habitat, and highlights nonlinear responses of coastal carbonate parameters to ocean acidification relevant for water quality management.

Seagrass habitat metabolism increases short-term extremes and long-term offset of CO2 under future ocean acidification

Science.gov (United States)

Pacella, Stephen R.; Brown, Cheryl A.; Waldbusser, George G.; Labiosa, Rochelle G.; Hales, Burke

2018-04-01

The role of rising atmospheric CO2 in modulating estuarine carbonate system dynamics remains poorly characterized, likely due to myriad processes driving the complex chemistry in these habitats. We reconstructed the full carbonate system of an estuarine seagrass habitat for a summer period of 2.5 months utilizing a combination of time-series observations and mechanistic modeling, and quantified the roles of aerobic metabolism, mixing, and gas exchange in the observed dynamics. The anthropogenic CO2 burden in the habitat was estimated for the years 1765–2100 to quantify changes in observed high-frequency carbonate chemistry dynamics. The addition of anthropogenic CO2 alters the thermodynamic buffer factors (e.g., the Revelle factor) of the carbonate system, decreasing the seagrass habitat’s ability to buffer natural carbonate system fluctuations. As a result, the most harmful carbonate system indices for many estuarine organisms [minimum pHT, minimum Ωarag, and maximum pCO2(s.w.)] change up to 1.8×, 2.3×, and 1.5× more rapidly than the medians for each parameter, respectively. In this system, the relative benefits of the seagrass habitat in locally mitigating ocean acidification increase with the higher atmospheric CO2 levels predicted toward 2100. Presently, however, these mitigating effects are mixed due to intense diel cycling of CO2 driven by aerobic metabolism. This study provides estimates of how high-frequency pHT, Ωarag, and pCO2(s.w.) dynamics are altered by rising atmospheric CO2 in an estuarine habitat, and highlights nonlinear responses of coastal carbonate parameters to ocean acidification relevant for water quality management.

Non-Volcanic release of CO2 in Italy: quantification, conceptual models and gas hazard

Science.gov (United States)

Chiodini, G.; Cardellini, C.; Caliro, S.; Avino, R.

2011-12-01

Central and South Italy are characterized by the presence of many reservoirs naturally recharged by CO2 of deep provenance. In the western sector, the reservoirs feed hundreds of gas emissions at the surface. Many studies in the last years were devoted to (i) elaborating a map of CO2 Earth degassing of the region; (ii) to asses the gas hazard; (iii) to develop methods suitable for the measurement of the gas fluxes from different types of emissions; (iv) to elaborate the conceptual model of Earth degassing and its relation with the seismic activity of the region and (v) to develop physical numerical models of CO2 air dispersion. The main results obtained are: 1) A general, regional map of CO2 Earth degassing in Central Italy has been elaborated. The total flux of CO2 in the area has been estimated in ~ 10 Mt/a which are released to the atmosphere trough numerous dangerous gas emissions or by degassing spring waters (~ 10 % of the CO2 globally estimated to be released by the Earth trough volcanic activity). 2) An on line, open access, georeferenced database of the main CO2 emissions (~ 250) was settled up (http://googas.ov.ingv.it). CO2 flux > 100 t/d characterise 14% of the degassing sites while CO2 fluxes from 100 t/d to 10 t/d have been estimated for about 35% of the gas emissions. 3) The sites of the gas emissions are not suitable for life: the gas causes many accidents to animals and people. In order to mitigate the gas hazard a specific model of CO2 air dispersion has been developed and applied to the main degassing sites. A relevant application regarded Mefite d'Ansanto, southern Apennines, which is the largest natural emission of low temperature CO2 rich gases, from non-volcanic environment, ever measured in the Earth (˜2000 t/d). Under low wind conditions, the gas flows along a narrow natural channel producing a persistent gas river which has killed over a period of time many people and animals. The application of the physical numerical model allowed us to

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.

Potential for iron oxides to control metal releases in CO2 sequestration scenarios

Science.gov (United States)

Berger, P.M.; Roy, W.R.

2011-01-01

The potential for the release of metals into groundwater following the injection of carbon dioxide (CO2) into the subsurface during carbon sequestration projects remains an open research question. Changing the chemical composition of even the relatively deep formation brines during CO2 injection and storage may be of concern because of the recognized risks associated with the limited potential for leakage of CO2-impacted brine to the surface. Geochemical modeling allows for proactive evaluation of site geochemistry before CO2 injection takes place to predict whether the release of metals from iron oxides may occur in the reservoir. Geochemical modeling can also help evaluate potential changes in shallow aquifers were CO2 leakage to occur near the surface. In this study, we created three batch-reaction models that simulate chemical changes in groundwater resulting from the introduction of CO2 at two carbon sequestration sites operated by the Midwest Geological Sequestration Consortium (MGSC). In each of these models, we input the chemical composition of groundwater samples into React??, and equilibrated them with selected mineral phases and CO 2 at reservoir pressure and temperature. The model then simulated the kinetic reactions with other mineral phases over a period of up to 100 years. For two of the simulations, the water was also at equilibrium with iron oxide surface complexes. The first model simulated a recently completed enhanced oil recovery (EOR) project in south-central Illinois in which the MGSC injected into, and then produced CO2, from a sandstone oil reservoir. The MGSC afterwards periodically measured the brine chemistry from several wells in the reservoir for approximately two years. The sandstone contains a relatively small amount of iron oxide, and the batch simulation for the injection process showed detectable changes in several aqueous species that were attributable to changes in surface complexation sites. After using the batch reaction

A physiological approach to oceanic processes and glacial-interglacial changes in atmospheric CO2

Directory of Open Access Journals (Sweden)

Josep L. Pelegrí

2008-03-01

Full Text Available One possible path for exploring the Earth’s far-from-equilibrium homeostasis is to assume that it results from the organisation of optimal pulsating systems, analogous to that in complex living beings. Under this premise it becomes natural to examine the Earth’s organisation using physiological-like variables. Here we identify some of these main variables for the ocean’s circulatory system: pump rate, stroke volume, carbon and nutrient arterial-venous differences, inorganic nutrients and carbon supply, and metabolic rate. The stroke volume is proportional to the water transported into the thermocline and deep oceans, and the arterial-venous differences occur between recently-upwelled deep waters and very productive high-latitudes waters, with atmospheric CO2 being an indicator of the arterial-venous inorganic carbon difference. The metabolic rate is the internal-energy flux (here expressed as flux of inorganic carbon in the upper ocean required by the system’s machinery, i.e. community respiration. We propose that the pump rate is set externally by the annual cycle, at one beat per year per hemisphere, and that the autotrophic ocean adjusts its stroke volume and arterial-venous differences to modify the internal-energy demand, triggered by long-period astronomical insolation cycles (external-energy supply. With this perspective we may conceive that the Earth’s interglacial-glacial cycle responds to an internal organisation analogous to that occurring in living beings during an exercise-recovery cycle. We use an idealised double-state metabolic model of the upper ocean (with the inorganic carbon/nutrients supply specified through the overturning rate and the steady-state inorganic carbon/nutrients concentrations to obtain the temporal evolution of its inorganic carbon concentration, which mimics the glacial-interglacial atmospheric CO2 pattern.

14CO2 measurements in maritime air over the Northern Indian Ocean

International Nuclear Information System (INIS)

Dutta, K.; Bhushan, R.; Somayajulu, B.L.K.

2002-01-01

14 C in the carbon dioxide of air overlying the Northern Indian Ocean was measured during the spring of 1993 to 1995 and 1997 to 1999. Considerable variations of 14 C over this region have been observed during this period, which reflect both regional and interannual variations. The interannual variations of 14 C of the tropospheric CO 2 over this region is found to correlate with the El Nino/Southern Oscillation (ENSO) events, with positive excursions of 14 C before the onset of warm phase of ENSO. (author)

Insight into the Global Carbon Cycle from Assimilation of Satellite CO2 measurements

Science.gov (United States)

Baker, D. F.

2017-12-01

A key goal of satellite CO2 measurements is to provide sufficient spatio-temporal coverage to constrain portions of the globe poorly observed by the in situ network, especially the tropical land regions. While systematic errors in both measurements and modeling remain a challenge, these satellite data are providing new insight into the functioning of the global carbon cycle, most notably across the recent 2015-16 En Niño. Here we interpret CO2 measurements from the GOSAT and OCO-2 satellites, as well as from the global in situ network (both surface sites and routine aircraft profiles), using a 4DVar-based global CO2 flux inversion across 2009-2017. The GOSAT data indicate that the tropical land regions are responsible for most of the observed global variability in CO2 across the last 8+ years. For the most recent couple of years where they overlap, the OCO-2 data give the same result, an +2 PgC/yr shift towards CO2 release in the ENSO warm phase, while disagreeing somewhat on the absolute value of the flux. The variability given by both these satellites disagrees with that given by an in situ-only inversion across the recent 2015-16 El Niño: the +2 PgC/yr shift from the satellites is double that given by the in situ data alone, suggesting that the more complete coverage is providing a more accurate view. For the current release of OCO-2 data (version 7), however, the flux results given by the OCO-2 land data (from both nadir- and glint-viewing modes) disagree significantly with those given by the ocean glint data; we examine the soon-to-be-released v8 data to assess whether these systematic retrieval errors have been reduced, and whether the corrected OCO-2 ocean data support the result from the land data. We discuss finer-scale features flux results given by the satellite data, and examine the importance of the flux prior, as well.

The impact on atmospheric CO2 of iron fertilization induced changes in the ocean's biological pump

Science.gov (United States)

Jin, X.; Gruber, N.; Frenzel, H.; Doney, S. C.; McWilliams, J. C.

2008-03-01

Using numerical simulations, we quantify the impact of changes in the ocean's biological pump on the air-sea balance of CO2 by fertilizing a small surface patch in the high-nutrient, low-chlorophyll region of the eastern tropical Pacific with iron. Decade-long fertilization experiments are conducted in a basin-scale, eddy-permitting coupled physical/biogeochemical/ecological model. In contrast to previous studies, we find that most of the dissolved inorganic carbon (DIC) removed from the euphotic zone by the enhanced biological export is replaced by uptake of CO2 from the atmosphere. Atmospheric uptake efficiencies, the ratio of the perturbation in air-sea CO2 flux to the perturbation in export flux across 100 m, integrated over 10 years, are 0.75 to 0.93 in our patch size-scale experiments. The atmospheric uptake efficiency is insensitive to the duration of the experiment. The primary factor controlling the atmospheric uptake efficiency is the vertical distribution of the enhanced biological production and export. Iron fertilization at the surface tends to induce production anomalies primarily near the surface, leading to high efficiencies. In contrast, mechanisms that induce deep production anomalies (e.g. altered light availability) tend to have a low uptake efficiency, since most of the removed DIC is replaced by lateral and vertical transport and mixing. Despite high atmospheric uptake efficiencies, patch-scale iron fertilization of the ocean's biological pump tends to remove little CO2 from the atmosphere over the decadal timescale considered here.

Program Developed for CO2 System Calculations (Program files: CO2SYS_calc_DOS_v1.05; CO2SYS_calc_XLS_v2.3; CO2SYS_calc_MAC_WIN; CO2SYS_calc_MATLAB_v1.1) (NCEI Accession 0164485)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — The program CO2SYS performs calculations relating parameters of the carbon dioxide (CO2) system in seawater and freshwater. The program uses two of the four...

Over-calcified forms of the coccolithophore Emiliania huxleyi in high-CO2 waters are not preadapted to ocean acidification

Science.gov (United States)

von Dassow, Peter; Díaz-Rosas, Francisco; Mahdi Bendif, El; Gaitán-Espitia, Juan-Diego; Mella-Flores, Daniella; Rokitta, Sebastian; John, Uwe; Torres, Rodrigo

2018-03-01

Marine multicellular organisms inhabiting waters with natural high fluctuations in pH appear more tolerant to acidification than conspecifics occurring in nearby stable waters, suggesting that environments of fluctuating pH hold genetic reservoirs for adaptation of key groups to ocean acidification (OA). The abundant and cosmopolitan calcifying phytoplankton Emiliania huxleyi exhibits a range of morphotypes with varying degrees of coccolith mineralization. We show that E. huxleyi populations in the naturally acidified upwelling waters of the eastern South Pacific, where pH drops below 7.8 as is predicted for the global surface ocean by the year 2100, are dominated by exceptionally over-calcified morphotypes whose distal coccolith shield can be almost solid calcite. Shifts in morphotype composition of E. huxleyi populations correlate with changes in carbonate system parameters. We tested if these correlations indicate that the hyper-calcified morphotype is adapted to OA. In experimental exposures to present-day vs. future pCO2 (400 vs. 1200 µatm), the over-calcified morphotypes showed the same growth inhibition (-29.1±6.3 %) as moderately calcified morphotypes isolated from non-acidified water (-30.7±8.8 %). Under the high-CO2-low-pH condition, production rates of particulate organic carbon (POC) increased, while production rates of particulate inorganic carbon (PIC) were maintained or decreased slightly (but not significantly), leading to lowered PIC / POC ratios in all strains. There were no consistent correlations of response intensity with strain origin. The high-CO2-low-pH condition affected coccolith morphology equally or more strongly in over-calcified strains compared to moderately calcified strains. High-CO2-low-pH conditions appear not to directly select for exceptionally over-calcified morphotypes over other morphotypes, but perhaps indirectly by ecologically correlated factors. More generally, these results suggest that oceanic planktonic

Impact production of CO2 by the Cretaceous/Tertiary extinction bolide and the resultant heating of the earth

Science.gov (United States)

O'Keefe, John D.; Ahrens, Thomas J.

1989-01-01

Various observations and data demonstrate that sea level at the end of the Cretaceous was 150-200 m higher than at present, suggesting the possibility that the extinction bolide struck a shallow marine carbonate-rich sedimentary section. It is shown here that the impact of such a bolide (about 5 km in radius) onto a carbonate-rich terrane would increase the CO2 content of the atmosphere by a factor of two to ten. Additional dissolution of CO2 from the ocean's photic zone could release much larger quantities of CO2. The impact-induced release of CO2, by itself, would enhance atmospheric greenhouse heating and give rise to a worldwide increase in temperature from 2 K to 10 K for periods of 10,000 to 100,000 years.

Crustacean zooplankton release copious amounts of dissolved organic matter as taurine in the ocean.

Science.gov (United States)

Clifford, Elisabeth L; Hansell, Dennis A; Varela, Marta M; Nieto-Cid, Mar; Herndl, Gerhard J; Sintes, Eva

2017-11-01

Taurine (Tau), an amino acid-like compound, is present in almost all marine metazoans including crustacean zooplankton. It plays an important physiological role in these organisms and is released into the ambient water throughout their life cycle. However, limited information is available on the release rates by marine organisms, the concentrations and turnover of Tau in the ocean. We determined dissolved free Tau concentrations throughout the water column and its release by abundant crustacean mesozooplankton at two open ocean sites (Gulf of Alaska and North Atlantic). At both locations, the concentrations of dissolved free Tau were in the low nM range (up to 15.7 nM) in epipelagic waters, declining sharply in the mesopelagic to about 0.2 nM and remaining fairly stable throughout the bathypelagic waters. Pacific amphipod-copepod assemblages exhibited lower dissolved free Tau release rates per unit biomass (0.8 ± 0.4 μmol g -1 C-biomass h -1 ) than Atlantic copepods (ranging between 1.3 ± 0.4 μmol g -1 C-biomass h -1 and 9.5 ± 2.1 μmol g -1 C-biomass h -1 ), in agreement with the well-documented inverse relationship between biomass-normalized excretion rates and body size. Our results indicate that crustacean zooplankton might contribute significantly to the dissolved organic matter flux in marine ecosystems via dissolved free Tau release. Based on the release rates and assuming steady state dissolved free Tau concentrations, turnover times of dissolved free Tau range from 0.05 d to 2.3 d in the upper water column and are therefore similar to those of dissolved free amino acids. This rapid turnover indicates that dissolved free Tau is efficiently consumed in oceanic waters, most likely by heterotrophic bacteria.

Metal release from sandstones under experimentally and numerically simulated CO2 leakage conditions.

Science.gov (United States)

Kirsch, Katie; Navarre-Sitchler, Alexis K; Wunsch, Assaf; McCray, John E

2014-01-01

Leakage of CO2 from a deep storage formation into an overlying potable aquifer may adversely impact water quality and human health. Understanding CO2-water-rock interactions is therefore an important step toward the safe implementation of geologic carbon sequestration. This study targeted the geochemical response of siliclastic rock, specifically three sandstones of the Mesaverde Group in northwestern Colorado. To test the hypothesis that carbonate minerals, even when present in very low levels, would be the primary source of metals released into a CO2-impacted aquifer, two batch experiments were conducted. Samples were reacted for 27 days with water and CO2 at partial pressures of 0.01 and 1 bar, representing natural background levels and levels expected in an aquifer impacted by a small leakage, respectively. Concentrations of major (e.g., Ca, Mg) and trace (e.g., As, Ba, Cd, Fe, Mn, Pb, Sr, U) elements increased rapidly after CO2 was introduced into the system, but did not exceed primary Maximum Contaminant Levels set by the U.S. Environmental Protection Agency. Results of sequential extraction suggest that carbonate minerals, although volumetrically insignificant in the sandstone samples, are the dominant source of mobile metals. This interpretation is supported by a simple geochemical model, which could simulate observed changes in fluid composition through CO2-induced calcite and dolomite dissolution.

CO2 impulse response curves for GWP calculations

International Nuclear Information System (INIS)

Jain, A.K.; Wuebbles, D.J.

1993-01-01

The primary purpose of Global Warming Potential (GWP) is to compare the effectiveness of emission strategies for various greenhouse gases to those for CO 2 , GWPs are quite sensitive to the amount of CO 2 . Unlike all other gases emitted in the atmosphere, CO 2 does not have a chemical or photochemical sink within the atmosphere. Removal of CO 2 is therefore dependent on exchanges with other carbon reservoirs, namely, ocean and terrestrial biosphere. The climatic-induced changes in ocean circulation or marine biological productivity could significantly alter the atmospheric CO 2 lifetime. Moreover, continuing forest destruction, nutrient limitations or temperature induced increases of respiration could also dramatically change the lifetime of CO 2 in the atmosphere. Determination of the current CO 2 sinks, and how these sinks are likely to change with increasing CO 2 emissions, is crucial to the calculations of GWPs. It is interesting to note that the impulse response function is sensitive to the initial state of the ocean-atmosphere system into which CO 2 is emitted. This is due to the fact that in our model the CO 2 flux from the atmosphere to the mixed layer is a nonlinear function of ocean surface total carbon

Development of a CO2 releasing co-formulation 1 based on starch, Saccharomyces cerevisiae and Beauveria bassiana attractive towards western corn rootworm larvae

Science.gov (United States)

CO2 is known as an attractant for many soil-dwelling pests. To implement an attract-and-kill strategy for soil pest control, CO2 emitting formulations need to be developed. This work aimed at the development of a slow release bead system in order to bridge the gap between application and hatching of...

International Comprehensive Ocean-Atmosphere Data Set (ICOADS) with Enhanced Trimming, Release 3

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — This dataset contains the latest official release of International Comprehensive Ocean-Atmosphere Data Set (ICOADS) with Enhanced Trimming, provided in a common...

CO2 and circulation in the deglacial North Pacific

Science.gov (United States)

Taylor, B.; Rae, J. W. B.; Gray, W. R.; Rees-Owen, R. L.; Burke, A.

2017-12-01

The North Pacific is the largest carbon reservoir in the global ocean, but has not typically been thought to play an active role in deglacial CO2 rise based on its modern stratified state. Recent studies (Okazaki et al., 2010; Rae et al., 2014; Max et al., 2017), however, have suggested that a more dynamic circulation regime operated in the glacial and deglacial North Pacific and, as such, the role of the North Pacific in deglacial CO2 rise may have been underestimated. We present two new high-resolution boron isotope records of surface water pCO2 from the North West and North East Pacific spanning the last 22 kyrs. The two records show remarkable coherence over key intervals during the last deglaciation and highlight major changes over a number of abrupt climate events. At both sites, following the LGM, pCO2(sw) rises, coincident with a younging of North Pacific intermediate and deep waters. This suggests that increased local overturning mixed CO2-rich deep waters throughout the water column, likely contributing to CO2 outgassing during Heinrich Stadial 1 (HS1). Both records exhibit decreases in pCO2(sw) during the latter stages of HS1, which are immediately followed by a rapid increase in pCO2(sw) at the onset of the Bølling-Allerød (B/A). Radiocarbon and δ13C data indicate a collapse in North Pacific Intermediate Water formation at the onset of the B/A, which, combined with enhanced wind stress curl, would have allowed CO2-rich waters to mix into the surface ocean from intermediate-depths. The combination of high nutrient availability and a seasonally well-stratified mixed layer likely led to the abrupt increase in export productivity across the region; the excess surface water CO2 shows that alleviation of iron or light limitation could not have been its primary cause. Our new records highlight the importance of overturning circulation in the North Pacific in controlling productivity and CO2 release on glacial/interglacial timescales.

The impact on atmospheric CO2 of iron fertilization induced changes in the ocean's biological pump

Directory of Open Access Journals (Sweden)

J. C. McWilliams

2008-03-01

Full Text Available Using numerical simulations, we quantify the impact of changes in the ocean's biological pump on the air-sea balance of CO2 by fertilizing a small surface patch in the high-nutrient, low-chlorophyll region of the eastern tropical Pacific with iron. Decade-long fertilization experiments are conducted in a basin-scale, eddy-permitting coupled physical/biogeochemical/ecological model. In contrast to previous studies, we find that most of the dissolved inorganic carbon (DIC removed from the euphotic zone by the enhanced biological export is replaced by uptake of CO2 from the atmosphere. Atmospheric uptake efficiencies, the ratio of the perturbation in air-sea CO2 flux to the perturbation in export flux across 100 m, integrated over 10 years, are 0.75 to 0.93 in our patch size-scale experiments. The atmospheric uptake efficiency is insensitive to the duration of the experiment. The primary factor controlling the atmospheric uptake efficiency is the vertical distribution of the enhanced biological production and export. Iron fertilization at the surface tends to induce production anomalies primarily near the surface, leading to high efficiencies. In contrast, mechanisms that induce deep production anomalies (e.g. altered light availability tend to have a low uptake efficiency, since most of the removed DIC is replaced by lateral and vertical transport and mixing. Despite high atmospheric uptake efficiencies, patch-scale iron fertilization of the ocean's biological pump tends to remove little CO2 from the atmosphere over the decadal timescale considered here.

Laboratory Investigations in Support of Carbon Dioxide-Limestone Sequestration in the Ocean

Energy Technology Data Exchange (ETDEWEB)

Dan Golomb; Eugene Barry; David Ryan; Stephen Pennell; Peter Swett; Huishan Duan; Michael Woods

2006-04-01

heavier than ambient seawater, hence the plume will sink to greater depth from the release point. Preliminary modeling indicates that an emulsion plume released at 500 m depth (the minimum depth required to prevent liquid CO{sub 2} flashing into vapor) may sink hundreds of meters before the plume comes to rest in the density stratified ocean water. Furthermore, tests in our laboratory showed that the emulsion is slightly alkaline, not acidic, because of the excess of CaCO{sub 3} particles present in the plume. Thus, the release of the CO{sub 2}-H{sub 2}OCaCO{sub 3} emulsion in the deep ocean is not likely to acidify the seawater around the release point. The possible acidification of seawater is the major environmental hazard if pure liquid CO{sub 2} were released in the deep ocean.

Global Ocean Surface Water Partial Pressure of CO2 Database: Measurements Performed During 1957-2016 (LDEO Database Version 2016) (NCEI Accession 0160492)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Approximately 10.8 million measurements of surface water pCO2 made over the global oceans during 1957-2016 have been processed to make a uniform data file in this...

Variability in the organic ligands released by Emiliania huxleyi under simulated ocean acidification conditions

Directory of Open Access Journals (Sweden)

Guillermo Samperio-Ramos

2017-12-01

Full Text Available The variability in the extracellular release of organic ligands by Emiliania huxleyi under four different pCO2 scenarios (225, 350, 600 and 900 μatm, was determined. Growth in the batch cultures was promoted by enriching them only with major nutrients and low iron concentrations. No chelating agents were added to control metal speciation. During the initial (IP, exponential (EP and steady (SP phases, extracellular release rates, normalized per cell and day, of dissolved organic carbon (DOCER, phenolic compounds (PhCER, dissolved combined carbohydrates (DCCHOER and dissolved uronic acids (DUAER in the exudates were determined. The growth rate decreased in the highest CO2 treatment during the IP (＜48 h, but later increased when the exposure was longer (more than 6 days. DOCER did not increase significantly with high pCO2. Although no relationship was observed between DCCHOER and the CO2 conditions, DCCHO was a substantial fraction of the freshly released organic material, accounting for 18% to 37%, in EP, and 14% to 23%, in SP, of the DOC produced. Growth of E. huxleyi induced a strong response in the PhCER and DUAER. While in EP, PhCER were no detected, the DUAER remained almost constant for all CO2 treatments. Increases in the extracellular release of these organic ligands during SP were most pronounced under high pCO2 conditions. Our results imply that, during the final growth stage of E. huxleyi, elevated CO2 conditions will increase its excretion of acid polysaccharides and phenolic compounds, which may affect the biogeochemical behavior of metals in seawater.

Radiocarbon constraints on the glacial ocean circulation and its impact on atmospheric CO2

Science.gov (United States)

Skinner, L. C.; Primeau, F.; Freeman, E.; de la Fuente, M.; Goodwin, P. A.; Gottschalk, J.; Huang, E.; McCave, I. N.; Noble, T. L.; Scrivner, A. E.

2017-01-01

While the ocean’s large-scale overturning circulation is thought to have been significantly different under the climatic conditions of the Last Glacial Maximum (LGM), the exact nature of the glacial circulation and its implications for global carbon cycling continue to be debated. Here we use a global array of ocean–atmosphere radiocarbon disequilibrium estimates to demonstrate a ∼689±53 14C-yr increase in the average residence time of carbon in the deep ocean at the LGM. A predominantly southern-sourced abyssal overturning limb that was more isolated from its shallower northern counterparts is interpreted to have extended from the Southern Ocean, producing a widespread radiocarbon age maximum at mid-depths and depriving the deep ocean of a fast escape route for accumulating respired carbon. While the exact magnitude of the resulting carbon cycle impacts remains to be confirmed, the radiocarbon data suggest an increase in the efficiency of the biological carbon pump that could have accounted for as much as half of the glacial–interglacial CO2 change. PMID:28703126

Global carbon - nitrogen - phosphorus cycle interactions: A key to solving the atmospheric CO2 balance problem?

Science.gov (United States)

Peterson, B. J.; Mellillo, J. M.

1984-01-01

If all biotic sinks of atmospheric CO2 reported were added a value of about 0.4 Gt C/yr would be found. For each category, a very high (non-conservative) estimate was used. This still does not provide a sufficient basis for achieving a balance between the sources and sinks of atmospheric CO2. The bulk of the discrepancy lies in a combination of errors in the major terms, the greatest being in a combination of errors in the major terms, the greatest being in the net biotic release and ocean uptake segments, but smaller errors or biases may exist in calculations of the rate of atmospheric CO2 increase and total fossil fuel use as well. The reason why biotic sinks are not capable of balancing the CO2 increase via nutrient-matching in the short-term is apparent from a comparison of the stoichiometry of the sources and sinks. The burning of fossil fuels and forest biomass releases much more CO2-carbon than is sequestered as organic carbon.

Calcification rates of the Caribbean reef-building coral Siderastrea siderea adversely affected by both seawater warming and CO2-induced ocean acidification

Science.gov (United States)

Horvath, K. M.; Connolly, B. D.; Westfield, I. T.; Chow, E.; Castillo, K. D.; Ries, J. B.

2013-05-01

The Intergovernmental Panel on Climate Change (IPCC) predicts that atmospheric pCO2 will increase to ca. 550-950 ppm by the end of the century, primarily due to the anthropogenic combustion of fossil fuels, deforestation, and cement production. This is predicted to cause SST to increase by 1-3 °C and seawater pH to decrease by 0.1-0.3 units. Laboratory studies have shown that warming depresses calcification rates of scleractinian corals and that acidification yields mixed effects on coral calcification. With both warming and ocean acidification predicted for the next century, we must constrain the interactive effects of these two CO2-induced stressors on scleractinian coral calcification. Here, we present the results of experiments designed to assess the response of the scleractinian coral Siderastrea siderea to both ocean warming and acidification. Coral fragments (12/tank) were reared for 60 days under three temperatures (25.1± 0.02 °C, 28.0± 0.02 °C, 31.8± 0.02 °C) at near modern pCO2 (436 ± 7) and near the highest IPCC estimate for atmospheric pCO2 for the year 2100 AD (883 ± 16). Each temperature and pCO2 treatment was executed in triplicate and contained similarly sized S. Siderea fragments obtained from the same suite of coral colonies equitably distributed amongst the nearshore, backreef, and forereef zones of the Mesoamerican Barrier Reef System off the coast of southern Belize. Individual coral fragments were hand fed Artemia sp. to satiation twice weekly. Weekly seawater samples (250 ml) were collected and analyzed for dissolved inorganic carbon via coulometry and total alkalinity via closed-cell potentiometric titration. Seawater pCO2, pH, carbonate ion concentration, bicarbonate ion concentration, aqueous CO2, and aragonite saturation state (ΩA) were calculated with the program CO2SYS. Under near-modern atmospheric pCO2 of ca. 436 ± 7 ppm, seawater warming from 25 to 28 to 32°C caused coral calcification rates (estimated from change in

Global Ocean Surface Water Partial Pressure of CO₂ Database: Measurements Performed During 1968-2007 (Version 2007)

Energy Technology Data Exchange (ETDEWEB)

Kozyr, Alex [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Carbon Dioxide Information Analysis Center

2008-09-30

More than 4.1 million measurements of surface water partial pressure of CO₂ obtained over the global oceans during 1968-2007 are listed in the Lamont-Doherty Earth Observatory (LDEO) database, which includes open ocean and coastal water measurements. The data assembled include only those measured by equilibrator-CO₂ analyzer systems and have been quality-controlled based on the stability of the system performance, the reliability of calibrations for CO₂ analysis, and the internal consistency of data. To allow re-examination of the data in the future, a number of measured parameters relevant to pCO₂ measurements are listed. The overall uncertainty for the pCO₂ values listed is estimated to be ± 2.5 µatm on the average. For simplicity and for ease of reference, this version is referred to as 2007, meaning that data collected through 31 December 2007 has been included. It is our intention to update this database annually. There are 37 new cruise/ship files in this update. In addition, some editing has been performed on existing files so this should be considered a V2007 file. Also we have added a column reporting the partial pressure of CO₂ in seawater in units of Pascals. The data presented in this database include the analyses of partial pressure of CO₂ (pCO₂), sea surface temperature (SST), sea surface salinity (SSS), pressure of the equilibration, and barometric pressure in the outside air from the ship’s observation system. The global pCO₂ data set is available free of charge as a numeric data package (NDP) from the Carbon Dioxide Information Analysis Center (CDIAC). The NDP consists of the oceanographic data files and this printed documentation, which describes the procedures and methods used to obtain the data.

Monitoring and assessment of ocean acidification in the Arctic Ocean-A scoping paper

Science.gov (United States)

Robbins, Lisa L.; Yates, Kimberly K.; Feely, Richard; Fabry, Victoria

2010-01-01

Carbon dioxide (CO2) in the atmosphere is absorbed at the ocean surface 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. 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 (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. The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

Large CO2 and CH4 release from a flooded formerly drained fen

Science.gov (United States)

Sachs, T.; Franz, D.; Koebsch, F.; Larmanou, E.; Augustin, J.

2016-12-01

Drained peatlands are usually strong carbon dioxide (CO2) sources. In Germany, up to 4.5 % of the national CO2 emissions are estimated to be released from agriculturally used peatlands and for some peatland-rich northern states, such as Mecklenburg-Western Pomerania, this share increases to about 20%. Reducing this CO2 source and restoring the peatlands' natural carbon sink is one objective of large-scale nature protection and restoration measures, in which 37.000 ha of drained and degraded peatlands in Mecklenburg-Western Pomerania are slated for rewetting. It is well known, however, that in the initial phase of rewetting, a reduction of the CO2 source strength is usually accompanied by an increase in CH4 emissions. Thus, whether and when the intended effects of rewetting with regard to greenhouse gases are achieved, depends on the balance of CO2 and CH4 fluxes and on the duration of the initial CH4 emission phase. In 2013, a new Fluxnet site went online at a flooded formerly drained river valley fen site near Zarnekow, NE Germany (DE-Zrk), to investigate the combined CO2 and CH4 dynamics at such a heavily degraded and rewetted peatland. The site is dominated by open water with submerged and floating vegetation and surrounding Typha latifolia.Nine year after rewetting, we found large CH4 emissions of 53 g CH4 m-2 a-1 from the open water area, which are 4-fold higher than from the surrounding vegetation zone (13 g CH4 m-2 a-1). Surprisingly, both the open water and the vegetated area were net CO2 sources of 158 and 750 g CO2 m-2 a-1, respectively. Unusual meteorological conditions with a warm and dry summer and a mild winter might have facilitated high respiration rates, particularly from temporally non-inundated organic mud in the vegetation zone.

Source strength and dispersion of CO2 releases from high-pressure pipelines: CFD model using real gas equation of state

International Nuclear Information System (INIS)

Liu, Xiong; Godbole, Ajit; Lu, Cheng; Michal, Guillaume; Venton, Philip

2014-01-01

Highlights: • Validated CFD models for decompression and dispersion of CO 2 releases from pipelines. • Incorporation of real gas EOS into CFD code for source strength estimation. • Demonstration of better performance of SST k–ω turbulence model for jet flow. • Demonstration of better performance of real gas EOS compared to ideal gas EOS. • Demonstration of superiority of CFD models over a commercial risk assessment package. - Abstract: Transportation of CO 2 in high-pressure pipelines forms a crucial link in the ever-increasing application of Carbon Capture and Storage (CCS) technologies. An unplanned release of CO 2 from a pipeline presents a risk to human and animal populations and the environment. Therefore it is very important to develop a deeper understanding of the atmospheric dispersion of CO 2 before the deployment of CO 2 pipelines, to allow the appropriate safety precautions to be taken. This paper presents a two-stage Computational Fluid Dynamics (CFD) study developed (1) to estimate the source strength, and (2) to simulate the subsequent dispersion of CO 2 in the atmosphere, using the source strength estimated in stage (1). The Peng–Robinson (PR) EOS was incorporated into the CFD code. This enabled accurate modelling of the CO 2 jet to achieve more precise source strength estimates. The two-stage simulation approach also resulted in a reduction in the overall computing time. The CFD models were validated against experimental results from the British Petroleum (BP) CO 2 dispersion trials, and also against results produced by the risk management package Phast. Compared with the measurements, the CFD simulation results showed good agreement in both source strength and dispersion profile predictions. Furthermore, the effect of release direction on the dispersion was studied. The presented research provides a viable method for the assessment of risks associated with CCS

Processes governing transient responses of the deep ocean buoyancy budget to a doubling of CO2

Science.gov (United States)

Palter, J. B.; Griffies, S. M.; Hunter Samuels, B. L.; Galbraith, E. D.; Gnanadesikan, A.

2012-12-01

Recent observational analyses suggest there is a temporal trend and high-frequency variability in deep ocean buoyancy in the last twenty years, a phenomenon reproduced even in low-mixing models. Here we use an earth system model (GFDL's ESM2M) to evaluate physical processes that influence buoyancy (and thus steric sea level) budget of the deep ocean in quasi-steady state and under a doubling of CO2. A new suite of model diagnostics allows us to quantitatively assess every process that influences the buoyancy budget and its temporal evolution, revealing surprising dynamics governing both the equilibrium budget and its transient response to climate change. The results suggest that the temporal evolution of the deep ocean contribution to sea level rise is due to a diversity of processes at high latitudes, whose net effect is then advected in the Eulerian mean flow to mid and low latitudes. In the Southern Ocean, a slowdown in convection and spin up of the residual mean advection are approximately equal players in the deep steric sea level rise. In the North Atlantic, the region of greatest deep steric sea level variability in our simulations, a decrease in mixing of cold, dense waters from the marginal seas and a reduction in open ocean convection causes an accumulation of buoyancy in the deep subpolar gyre, which is then advected equatorward.

Re-evaluating the 1940s CO2 plateau

Science.gov (United States)

Bastos, Ana; Ciais, Philippe; Barichivich, Jonathan; Bopp, Laurent; Brovkin, Victor; Gasser, Thomas; Peng, Shushi; Pongratz, Julia; Viovy, Nicolas; Trudinger, Cathy M.

2016-09-01

The high-resolution CO2 record from Law Dome ice core reveals that atmospheric CO2 concentration stalled during the 1940s (so-called CO2 plateau). Since the fossil-fuel emissions did not decrease during the period, this stalling implies the persistence of a strong sink, perhaps sustained for as long as a decade or more. Double-deconvolution analyses have attributed this sink to the ocean, conceivably as a response to the very strong El Niño event in 1940-1942. However, this explanation is questionable, as recent ocean CO2 data indicate that the range of variability in the ocean sink has been rather modest in recent decades, and El Niño events have generally led to higher growth rates of atmospheric CO2 due to the offsetting terrestrial response. Here, we use the most up-to-date information on the different terms of the carbon budget: fossil-fuel emissions, four estimates of land-use change (LUC) emissions, ocean uptake from two different reconstructions, and the terrestrial sink modelled by the TRENDY project to identify the most likely causes of the 1940s plateau. We find that they greatly overestimate atmospheric CO2 growth rate during the plateau period, as well as in the 1960s, in spite of giving a plausible explanation for most of the 20th century carbon budget, especially from 1970 onwards. The mismatch between reconstructions and observations during the CO2 plateau epoch of 1940-1950 ranges between 0.9 and 2.0 Pg C yr-1, depending on the LUC dataset considered. This mismatch may be explained by (i) decadal variability in the ocean carbon sink not accounted for in the reconstructions we used, (ii) a further terrestrial sink currently missing in the estimates by land-surface models, or (iii) LUC processes not included in the current datasets. Ocean carbon models from CMIP5 indicate that natural variability in the ocean carbon sink could explain an additional 0.5 Pg C yr-1 uptake, but it is unlikely to be higher. The impact of the 1940-1942 El Niño on the

Development of thermosensitive poly(n-isopropylacrylamide-co-((2-dimethylamino) ethyl methacrylate))-based nanoparticles for controlled drug release

Energy Technology Data Exchange (ETDEWEB)

Peng, Cheng-Liang; Luo, Tsai-Yueh; Lin, Wuu-Jyh [Isotope Application Division, Institute of Nuclear Energy Research, PO Box 3-27, Longtan Taoyuan 325, Taiwan (China); Tsai, Han-Min; Yang, Shu-Jyuan; Lin, Chia-Fu; Shieh, Ming-Jium, E-mail: soloman@ntu.edu.tw [Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No 1, Section 1, Jen-Ai Road, Taipei 10051, Taiwan (China)

2011-07-01

Thermosensitive nanoparticles based on poly(N-isopropylacrylamide-co-((2-dimethylamino)ethylmethacrylate)) (poly(NIPA-co-DMAEMA)) copolymers were successfully fabricated by free radical polymerization. The lower critical solution temperature (LCST) of the synthesized nanoparticles was 41 deg. C and a temperature above which would cause the nanoparticles to undergo a volume phase transition from 140 to 100 nm, which could result in the expulsion of encapsulated drugs. Therefore, we used the poly(NIPA-co-DMAEMA) nanoparticles as a carrier for the controlled release of a hydrophobic anticancer agent, 7-ethyl-10-hydroxy-camptothecin (SN-38). The encapsulation efficiency and loading content of SN-38-loaded nanoparticles at an SN-38/poly(NIPA-co-DMAEMA) ratio of 1/10 (D/P = 1/10) were about 80% and 6.293%, respectively. Moreover, the release profile of SN-38-loaded nanoparticles revealed that the release rate at 42 deg. C (above LCST) was higher than that at 37 deg. C (below LCST), which demonstrated that the release of SN-38 could be controlled by increasing the temperature. The cytotoxicity of the SN-38-loaded poly(NIPA-co-DMAEMA) nanoparticles was investigated in human colon cancer cells (HT-29) to compare with the treatment of an anticancer drug, Irinotecan (CPT-11). The antitumor efficacy evaluated in a C26 murine colon tumor model showed that the SN-38-loaded nanoparticles in combination with hyperthermia therapy efficiently suppressed tumor growth. The results indicate that these thermo-responsive nanoparticles are potential carriers for controlled drug delivery.

Southern Ocean biogeochemical control of glacial/interglacial carbon dioxide change

Science.gov (United States)

Sigman, D. M.

2014-12-01

in the way of a theory of glacial cycles that includes Southern Ocean-driven CO2 change. There are more compelling proposals for the causes of deglacial change, with a sharp reduction in North Atlantic deep water formation implicated as a trigger of increased surface/deep exchange in the Antarctic and the resulting release of CO2 to the atmosphere.

[Impacts of rice straw biochar on organic carbon and CO2 release in arable soil].

Science.gov (United States)

Ke, Yue-Jin; Hu, Xue-Yu; Yi, Qing; Yu, Zhong

2014-01-01

In order to investigate the stability of biochar and the effect of biochar when added into soil on soil organic carbon, a 130-day incubation experiment was conducted with rice straw biochar produced at 500 degrees C and 700 degrees C (RBC500 and RBC700) and with addition rates of 0% (control), 3%, 6% and 100% (pure biochar), to detect the change of total organic carbon (TOC), easily oxidized carbon (EOC) and status of CO2 release, following addition of biochar in arable soil. Results showed that: the content of both TOC and EOC in soil increased with biochar addition rates comparing with the control. RBC500 had greater contributions to both TOC and EOC increasing amounts than those of RBC700 under the same biochar addition rate. TOC contents of all treatments decreased during the initial 30 days with the largest decreasing amplitude of 15.8%, and tended to be stable in late incubation stages. Same to that of TOC, EOC contents of all treatments also tended to remain stable after 30 days, but in the 30 days of early incubation, EOC in the soil decreased by 72.4% and 81.7% respectively when the added amount of RBC500 was 3% and 6% , while it was reduced by 61.3% and 69.8% respectively when the added amount of RBC700 was 3% and 6%. EOC contents of soil added with biochar produced at the same temperature were similar in the end of incubation. The reduction of soil EOC content in early incubation may be related to mineralization caused by labile fractions of biochar. During the 130-day incubation, the accumulated CO2 releases showed an order of soil and biochar mixtures soil could reduce CO2 release, the largest reduction amplitude is 41.05%. In a long time scale, biochar as a soil amendment is favorable to the deduction of greenhouse gas release and soil carbon immobilization. Biochar could be used as a soil carbon sequestration carrier.

Millennial Variability of Eastern Equatorial Bottom Water Oxygenation and Atmospheric CO2 over the past 100 kyr

Science.gov (United States)

Marcantonio, F.; Loveley, M.; Wisler, M.; Hostak, R.; Hertzberg, J. E.; Schmidt, M. W.; Lyle, M. W.

2017-12-01

Storage of respired carbon in the deep ocean may play a significant role in lowering atmospheric CO2 concentrations by about 80 ppm during the last glacial maximum compared to pre-industrial times. The cause of this sequestration and the subsequent release of the deep respired carbon pool at the last termination remains elusive. Within the last glacial period, on millennial timescales, the relationship between the CO2 cycle and any waxing and waning of a deep respired pool also remains unclear. To further our understanding of the millennial variability in the storage of a deep-ocean respired carbon pool during the last glacial, we measure authigenic uranium and 230Th-derived non-lithogenic barium fluxes (xsBa flux) in two high-sedimentation-rate cores from the Panama Basin of the Eastern Equatorial Pacific (EEP) (8JC, 6° 14.0' N, 86° 02.6' W; 1993 m water depth; 17JC 00° 10.8' S, 85° 52.0' W; 2846 m water depth). Sediment authigenic U concentrations are controlled by the redox state of sediments which, in turn, is a function of the rain of organic material from the surface ocean and the oxygen content of bottom waters. At both 8JC and 17JC, the mismatch between xsBa fluxes, a proxy for the reconstruction of oceanic productivity, and authigenic uranium concentrations suggests that the primary control of the latter values is changes in bottom water oxygenation. Peak authigenic uranium concentrations occur during glacial periods MIS 2, 3, and 4, respectively, and are two to three times higher than those during interglacial periods, MIS 1 and 5. EEP bottom waters were likely suboxic during times of the last glacial period when atmospheric CO2 concentrations were at their lowest concentrations. In addition, the pattern of increased deep-water oxygenation during times of higher CO2 during the last glacial is similar to that reported in a study of authigenic U in sediments from the Antarctic Zone of the Southern Ocean (Jaccard et al., 2016). We suggest that a respired

Role of mesoscale eddies in the global ocean uptake of anthropogenic CO{sub 2}; Role des tourbillons de meso-echelle oceaniques dans la distribution et les flux air-mer de CO{sub 2} anthropique a l'echelle globale

Energy Technology Data Exchange (ETDEWEB)

Zouhair, Lachkar

2007-02-15

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{sub 2}, CFC-11 and bomb {delta}{sup 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 {delta}{sup 14}C uptake and storage. Yet for CFC-11 and anthropogenic CO{sub 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

Using the Bongwana natural CO2 release to understand leakage processes and develop monitoring

Science.gov (United States)

Jones, David; Johnson, Gareth; Hicks, Nigel; Bond, Clare; Gilfillan, Stuart; Kremer, Yannick; Lister, Bob; Nkwane, Mzikayise; Maupa, Thulani; Munyangane, Portia; Robey, Kate; Saunders, Ian; Shipton, Zoe; Pearce, Jonathan; Haszeldine, Stuart

2016-04-01

Natural CO2 leakage along the Bongwana Fault in South Africa is being studied to help understand processes of CO2 leakage and develop monitoring protocols. The Bongwana Fault crops out over approximately 80 km in KwaZulu-Natal province, South Africa. In outcrop the fault is expressed as a broad fracture corridor in Dwyka Tillite, with fractures oriented approximately N-S. Natural emissions of CO2 occur at various points along the fault, manifest as travertine cones and terraces, bubbling in the rivers and as gas fluxes through soil. Exposed rock outcrop shows evidence for Fe-staining around fractures and is locally extensively kaolinitised. The gas has also been released through a shallow water well, and was exploited commercially in the past. Preliminary studies have been carried out to better document the surface emissions using near surface gas monitoring, understand the origin of the gas through major gas composition and stable and noble gas isotopes and improve understanding of the structural controls on gas leakage through mapping. In addition the impact of the leaking CO2 on local water sources (surface and ground) is being investigated, along with the seismic activity of the fault. The investigation will help to build technical capacity in South Africa and to develop monitoring techniques and plans for a future CO2 storage pilot there. Early results suggest that CO2 leakage is confined to a relatively small number of spatially-restricted locations along the weakly seismically active fault. Fracture permeability appears to be the main method by which the CO2 migrates to the surface. The bulk of the CO2 is of deep origin with a minor contribution from near surface biogenic processes as determined by major gas composition. Water chemistry, including pH, DO and TDS is notably different between CO2-rich and CO2-poor sites. Soil gas content and flux effectively delineates the fault trace in active leakage sites. The fault provides an effective testing ground for

Long-term surface pCO2 trends from observations and models

International Nuclear Information System (INIS)

Tjiputra, Jerry F.; Olsen, Are; Heinze, Christoph; Bopp, Laurent; Roy, Tilla

2014-01-01

We estimate regional long-term surface ocean pCO 2 growth rates using all available underway and bottled biogeochemistry data collected over the past four decades. These observed regional trends are compared with those simulated by five state-of-the-art Earth system models over the historical period. Oceanic pCO 2 growth rates faster than the atmospheric growth rates indicate decreasing atmospheric CO 2 uptake, while ocean pCO 2 growth rates slower than the atmospheric growth rates indicate increasing atmospheric CO 2 uptake. Aside from the western sub-polar North Pacific and the subtropical North Atlantic, our analysis indicates that the current observation-based basin-scale trends may be underestimated, indicating that more observations are needed to determine the trends in these regions. Encouragingly, good agreement between the simulated and observed pCO 2 trends is found when the simulated fields are sub sampled with the observational coverage. In agreement with observations, we see that the simulated pCO 2 trends are primarily associated with the increase in surface dissolved inorganic carbon (DIC) associated with atmospheric carbon uptake, and in part by warming of the sea surface. Under the RCP8.5 future scenario, DIC continues to be the dominant driver of pCO 2 trends, with little change in the relative contribution of SST. However, the changes in the hydrological cycle play an increasingly important role. For the contemporary (1970-2011) period, the simulated regional pCO 2 trends are lower than the atmospheric growth rate over 90% of the ocean. However, by year 2100 more than 40% of the surface ocean area has a higher oceanic pCO 2 trend than the atmosphere, implying a reduction in the atmospheric CO 2 uptake rate. The fastest pCO 2 growth rates are projected for the sub-polar North Atlantic, while the high-latitude Southern Ocean and eastern equatorial Pacific have the weakest growth rates, remaining below the atmospheric pCO 2 growth rate. Our work

Long-term surface pCO2 trends from observations and models

Directory of Open Access Journals (Sweden)

Jerry F. Tjiputra

2014-05-01

Full Text Available We estimate regional long-term surface ocean pCO2 growth rates using all available underway and bottled biogeochemistry data collected over the past four decades. These observed regional trends are compared with those simulated by five state-of-the-art Earth system models over the historical period. Oceanic pCO2 growth rates faster than the atmospheric growth rates indicate decreasing atmospheric CO2 uptake, while ocean pCO2 growth rates slower than the atmospheric growth rates indicate increasing atmospheric CO2 uptake. Aside from the western subpolar North Pacific and the subtropical North Atlantic, our analysis indicates that the current observation-based basin-scale trends may be underestimated, indicating that more observations are needed to determine the trends in these regions. Encouragingly, good agreement between the simulated and observed pCO2 trends is found when the simulated fields are subsampled with the observational coverage. In agreement with observations, we see that the simulated pCO2 trends are primarily associated with the increase in surface dissolved inorganic carbon (DIC associated with atmospheric carbon uptake, and in part by warming of the sea surface. Under the RCP8.5 future scenario, DIC continues to be the dominant driver of pCO2 trends, with little change in the relative contribution of SST. However, the changes in the hydrological cycle play an increasingly important role. For the contemporary (1970–2011 period, the simulated regional pCO2 trends are lower than the atmospheric growth rate over 90% of the ocean. However, by year 2100 more than 40% of the surface ocean area has a higher oceanic pCO2 trend than the atmosphere, implying a reduction in the atmospheric CO2 uptake rate. The fastest pCO2 growth rates are projected for the subpolar North Atlantic, while the high-latitude Southern Ocean and eastern equatorial Pacific have the weakest growth rates, remaining below the atmospheric pCO2 growth rate. Our work

Putting prey and predator into the CO2 equation--qualitative and quantitative effects of ocean acidification on predator-prey interactions.

Science.gov (United States)

Ferrari, Maud C O; McCormick, Mark I; Munday, Philip L; Meekan, Mark G; Dixson, Danielle L; Lonnstedt, Öona; Chivers, Douglas P

2011-11-01

Little is known about the impact of ocean acidification on predator-prey dynamics. Herein, we examined the effect of carbon dioxide (CO(2)) on both prey and predator by letting one predatory reef fish interact for 24 h with eight small or large juvenile damselfishes from four congeneric species. Both prey and predator were exposed to control or elevated levels of CO(2). Mortality rate and predator selectivity were compared across CO(2) treatments, prey size and species. Small juveniles of all species sustained greater mortality at high CO(2) levels, while large recruits were not affected. For large prey, the pattern of prey selectivity by predators was reversed under elevated CO(2). Our results demonstrate both quantitative and qualitative consumptive effects of CO(2) on small and larger damselfish recruits respectively, resulting from CO(2)-induced behavioural changes likely mediated by impaired neurological function. This study highlights the complexity of predicting the effects of climate change on coral reef ecosystems. © 2011 Blackwell Publishing Ltd/CNRS.

Ocean Acidification: Adaptive Challenge or Extinction Threat?

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Caldeira, K.

2012-12-01

Most of the carbon dioxide that we emit to this atmosphere through fossil-fuel burning and deforestation is ultimately absorbed by the oceans. The effects of excess carbon dioxide on the inorganic chemistry of the ocean are largely well understood, but it is less clear what these chemical changes mean for the future of marine biota. Excess dissolved CO2 increases hydrogen-ion concentration (i.e., decreases pH) and decreases carbonate-ion concentrations, affecting the chemical speciation of nutrients and other chemicals dissolved in the ocean, and affecting the ability of organisms to form calcium carbonate shells or skeletons. Some organisms, such as corals, develop shells or skeletons made from aragonite, a particularly soluble form of calcium carbonate. The uptake of O2 and the release of CO2 from the blood of fish are affected by pH, with lower pH leading to a decrease in both O2 uptake and CO2 release. Of these concerns, the effects of excess CO2 on calcification may be the most worrisome. Doubling or quadrupling of atmospheric CO2 content within the space of a few centuries means doubling or quadrupling hydrogen-ion concentrations and halving or quartering the carbonate-ion concentration within a few centuries. Experiments and theory indicate that chemical changes of this magnitude could have important biotic consequences. Changes of this magnitude and rapidity have not occurred on this planet with the possible exception of various paroxysmal extreme events buried deep in Earth history. Most major changes to ocean chemistry occurred over millions of years allowing (i) seawater chemistry to be in approximate equilibrium with respect to riverine and sedimentary fluxes and (ii) marine biota to adapt in evolutionary time. Man's great geochemical experiment will go on at global scale for thousands of years. But experiments can be done in the laboratory in small tanks or in the sea in small enclosures only for limited periods of time. It is difficult to infer from

Evaluation through column leaching tests of metal release from contaminated estuarine sediment subject to CO2 leakages from Carbon Capture and Storage sites

International Nuclear Information System (INIS)

Payán, M. Cruz; Galan, Berta; Coz, Alberto; Vandecasteele, Carlo; Viguri, Javier R.

2012-01-01

The pH change and the release of organic matter and metals from sediment, due to the potential CO 2 acidified seawater leakages from a CCS (Carbon Capture and Storage) site are presented. Column leaching test is used to simulate a scenario where a flow of acidified seawater is in contact with recent contaminated sediment. The behavior of pH, dissolved organic carbon (DOC) and metals As, Cd, Cr, Cu, Ni, Pb, Zn, with liquid to solid (L/S) ratio and pH is analyzed. A stepwise strategy using empirical expressions and a geochemical model was conducted to fit experimental release concentrations. Despite the neutralization capacity of the seawater-carbonate rich sediment system, important acidification and releases are expected at local scale at lower pH. The obtained results would be relevant as a line of evidence input of CCS risk assessment, in an International context where strategies to mitigate the climate change would be applied. - Highlights: ► Tier structured approach for assessment of the release of metals from sediment. ► Standard column leaching test to simulate CO 2 acidified seawater CCS leakages. ► Metal and DOC release from marine sediment in contact to CO 2 acidified seawater. ► From empirical to geochemical modeling approaches of DOC and metals release in column tests. ► Contamination line of evidence input of CCS risk assessment. - Column metal release from CO 2 acidified seawater leakages in contact with estuarine contaminated sediment in CCS sites

Development of a calcium phosphate co-precipitate/poly(lactide-co-glycolide) DNA delivery system: release kinetics and cellular transfection studies.

Science.gov (United States)

Kofron, Michelle D; Laurencin, Cato T

2004-06-01

One of the most common non-viral methods for the introduction of foreign deoxyribonucleic acid (DNA) into cultured cells is calcium phosphate co-precipitate transfection. This technique involves the encapsulation of DNA within a calcium phosphate co-precipitate, particulate addition to in vitro cell culture, endocytosis of the co-precipitate, and exogenous DNA expression by the transfected cell. In this study, we fabricated a novel non-viral gene transfer system by adsorbing DNA, encapsulated in calcium phosphate (DNA/Ca-P) co-precipitates, to biodegradable two- and three-dimensional poly(lactide-co-glycolide) matrices (2D-DNA/Ca-P/PLAGA, 3D-DNA/Ca-P/PLAGA). Co-precipitate release studies demonstrated an initial burst release over the first 48 h. By day 7, approximately 96% of the initially adsorbed DNA/Ca-P co-precipitate had been released. This was followed by low levels of co-precipitate release for 42 days. Polymerase chain reaction was used to demonstrate the ability of the released DNA containing co-precipitates to transfect SaOS-2 cells cultured in vitro on the 3D-DNA/Ca-P/PLAGA matrix and maintenance of the structural integrity of the exogenous DNA. In summary, a promising system for the incorporation and controlled delivery of exogenous genes encapsulated within a calcium phosphate co-precipitate from biodegradable polymeric matrices has been developed and may have applicability to the delivery of therapeutic genes and the transfection of other cell types.

Separate zones of sulfate and sulfide release from subducted mafic oceanic crust

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Tomkins, Andrew G.; Evans, Katy A.

2015-10-01

Liberation of fluids during subduction of oceanic crust is thought to transfer sulfur into the overlying sub-arc mantle. However, despite the importance of sulfur cycling through magmatic arcs to climate change, magma oxidation and ore formation, there has been little investigation of the metamorphic reactions responsible for sulfur release from subducting slabs. Here, we investigate the relative stability of anhydrite (CaSO4) and pyrite (FeS2) in subducted basaltic oceanic crust, the largest contributor to the subducted sulfur budget, to place constraints on the processes controlling sulfur release. Our analysis of anhydrite stability at high pressures suggests that this mineral should dominantly dissolve into metamorphic fluids released across the transition from blueschist to eclogite facies (∼450-650 °C), disappearing at lower temperatures on colder geothermal trajectories. In contrast, we suggest that sulfur release via conversion of pyrite to pyrrhotite occurs at temperatures above 750 °C. This higher temperature stability is indicated by the preservation of pyrite-bornite inclusions in coesite-bearing eclogites from the Sulu Belt in China, which reached temperatures of at least 750 °C. Thus, sulfur may be released from subducting slabs in two separate pulses; (1) varying proportions of SO2, HSO4- and H2S are released via anhydrite breakdown at the blueschist-eclogite transition, promoting oxidation of remaining silicates in some domains, and (2) H2S is released via pyrite breakdown well into the eclogite facies, which may in some circumstances coincide with slab melting or supercritical liquid generation driven by influx of serpentinite-derived fluids. These results imply that the metallogenic potential in the sub-arc mantle above the subducting slab varies as a function of subduction depth, having the greatest potential above the blueschist-eclogite transition given the association between oxidised magmas and porphyry Cu(-Au-Mo) deposits. We speculate

Short-term pain for long-term gain: seagrass communities increase short-term extremes and long-term offset of CO2 under future ocean acidification

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The impacts of ocean acidification in nearshore estuarine environments remain poorly characterized, despite these areas being some of the most ecologically, economically, and culturally important habitats in the global ocean. Here, we quantify how rising atmospheric CO2 from 1765...