Air-sea flux of CO2 in arctic coastal waters influenced by glacial melt water and sea ice

DEFF Research Database (Denmark)

Sejr, Mikael Kristian; Krause-Jensen, Dorte; Rysgaard, Søren

2011-01-01

Annual air–sea exchange ofCO2 inYoung Sound,NEGreenlandwas estimated using pCO2 surface-water measurements during summer (2006–2009) and during an ice-covered winter 2008. All surface pCO2 values were below atmospheric levels indicating an uptake of atmospheric CO2. During sea ice formation...... and thereby efficiently blocked air–sea CO2 exchange. During sea ice melt, dissolution of CaCO3 combined with primary production and strong stratification of the water column acted to lower surface-water pCO2 levels in the fjord. Also, a large input of glacial melt water containing geochemically reactive...... year-to-year variation in annual gas exchange....

Air-sea exchange of carbon dioxide

Energy Technology Data Exchange (ETDEWEB)

Bakker, D C.E.; De Baar, H J.W.; De Jong, E; Koning, F A [Netherlands Institute for Sea Research NIOZ, Den Burg Texel (Netherlands)

1996-12-31

The greenhouse gas carbon dioxide is emitted by anthropogenic activities. The oceans presumably serve as a net sink for 17 to 39% of these emissions. The objective of this project is to quantify more accurately the locality, seasonality and magnitude of the net air-sea flux of CO2 with emphasis on the South Atlantic Ocean. In situ measurements of the fugacity of CO2 in surface water and marine air, of total dissolved inorganic carbon, alkalinity and of air-sea exchange of CO2 have been made at four Atlantic crossings, in the Southern Ocean, in a Norwegian fjord and in the Dutch coastal zone. Skin temperature was detected during several of the cruises. The data collected in the course of the project support and refine previous findings. Variability of dissolved CO2 in surface water is related in a complex way to biological and physical factors. The carbonate equilibria cause dissolved gaseous CO2 to react in an intricate manner to disturbances. Dissolved gaseous CO2 hardly ever attains equilibrium with the atmospheric CO2 content by means of air-sea exchange, before a new disturbance occurs. Surface water fCO2 changes could be separated in those caused by seasonal warming and those by biological uptake in a Southern Ocean spring. Incorporation of a thermal skin effect and a change of the wind speed interval strongly increased the small net oceanic uptake for the area. The Atlantic crossings point to a relationship between water mass history and surface water CO2 characteristics. In particular, current flow and related heat fluxes leave their imprint on the concentration dissolved gaseous CO2 and on air-sea exchange. In the Dutch coastal zone hydrography and inorganic carbon characteristics of the water were heterogeneous, which yielded variable air-sea exchange of CO2. figs., tabs., refs.

Air-sea fluxes of CO2 and CH4 from the Penlee Point Atmospheric Observatory on the south-west coast of the UK

Science.gov (United States)

Yang, Mingxi; Bell, Thomas G.; Hopkins, Frances E.; Kitidis, Vassilis; Cazenave, Pierre W.; Nightingale, Philip D.; Yelland, Margaret J.; Pascal, Robin W.; Prytherch, John; Brooks, Ian M.; Smyth, Timothy J.

2016-05-01

We present air-sea fluxes of carbon dioxide (CO2), methane (CH4), momentum, and sensible heat measured by the eddy covariance method from the recently established Penlee Point Atmospheric Observatory (PPAO) on the south-west coast of the United Kingdom. Measurements from the south-westerly direction (open water sector) were made at three different sampling heights (approximately 15, 18, and 27 m above mean sea level, a.m.s.l.), each from a different period during 2014-2015. At sampling heights ≥ 18 m a.m.s.l., measured fluxes of momentum and sensible heat demonstrate reasonable ( ≤ ±20 % in the mean) agreement with transfer rates over the open ocean. This confirms the suitability of PPAO for air-sea exchange measurements in shelf regions. Covariance air-sea CO2 fluxes demonstrate high temporal variability. Air-to-sea transport of CO2 declined from spring to summer in both years, coinciding with the breakdown of the spring phytoplankton bloom. We report, to the best of our knowledge, the first successful eddy covariance measurements of CH4 emissions from a marine environment. Higher sea-to-air CH4 fluxes were observed during rising tides (20 ± 3; 38 ± 3; 29 ± 6 µmole m-2 d-1 at 15, 18, 27 m a.m.s.l.) than during falling tides (14 ± 2; 22 ± 2; 21 ± 5 µmole m-2 d-1), consistent with an elevated CH4 source from an estuarine outflow driven by local tidal circulation. These fluxes are a few times higher than the predicted CH4 emissions over the open ocean and are significantly lower than estimates from other aquatic CH4 hotspots (e.g. polar regions, freshwater). Finally, we found the detection limit of the air-sea CH4 flux by eddy covariance to be 20 µmole m-2 d-1 over hourly timescales (4 µmole m-2 d-1 over 24 h).

Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide

Directory of Open Access Journals (Sweden)

F. Ziska

2013-09-01

Full Text Available Volatile halogenated organic compounds containing bromine and iodine, which are naturally produced in the ocean, are involved in ozone depletion in both the troposphere and stratosphere. Three prominent compounds transporting large amounts of marine halogens into the atmosphere are bromoform (CHBr3, dibromomethane (CH2Br2 and methyl iodide (CH3I. The input of marine halogens to the stratosphere has been estimated from observations and modelling studies using low-resolution oceanic emission scenarios derived from top-down approaches. In order to improve emission inventory estimates, we calculate data-based high resolution global sea-to-air flux estimates of these compounds from surface observations within the HalOcAt (Halocarbons in the Ocean and Atmosphere database (https://halocat.geomar.de/. Global maps of marine and atmospheric surface concentrations are derived from the data which are divided into coastal, shelf and open ocean regions. Considering physical and biogeochemical characteristics of ocean and atmosphere, the open ocean water and atmosphere data are classified into 21 regions. The available data are interpolated onto a 1°×1° grid while missing grid values are interpolated with latitudinal and longitudinal dependent regression techniques reflecting the compounds' distributions. With the generated surface concentration climatologies for the ocean and atmosphere, global sea-to-air concentration gradients and sea-to-air fluxes are calculated. Based on these calculations we estimate a total global flux of 1.5/2.5 Gmol Br yr−1 for CHBr3, 0.78/0.98 Gmol Br yr−1 for CH2Br2 and 1.24/1.45 Gmol Br yr−1 for CH3I (robust fit/ordinary least squares regression techniques. Contrary to recent studies, negative fluxes occur in each sea-to-air flux climatology, mainly in the Arctic and Antarctic regions. "Hot spots" for global polybromomethane emissions are located in the equatorial region, whereas methyl iodide emissions are enhanced in the

Air–sea exchanges of CO2 in the world's coastal seas

Directory of Open Access Journals (Sweden)

C.-T. A. Chen

2013-10-01

Full Text Available The air–sea exchanges of CO2 in the world's 165 estuaries and 87 continental shelves are evaluated. Generally and in all seasons, upper estuaries with salinities of less than two are strong sources of CO2 (39 ± 56 mol C m−2 yr−1, positive flux indicates that the water is losing CO2 to the atmosphere; mid-estuaries with salinities of between 2 and 25 are moderate sources (17.5 ± 34 mol C m−2 yr−1 and lower estuaries with salinities of more than 25 are weak sources (8.4 ± 14 mol C m−2 yr−1. With respect to latitude, estuaries between 23.5 and 50° N have the largest flux per unit area (63 ± 101 mmol C m−2 d−1; these are followed by lower-latitude estuaries (23.5–0° S: 44 ± 29 mmol C m−2 d−1; 0–23.5° N: 39 ± 55 mmol C m−2 d−1, and then regions north of 50° N (36 ± 91 mmol C m−2 d−1. Estuaries south of 50° S have the smallest flux per unit area (9.5 ± 12 mmol C m−2 d−1. Mixing with low-pCO2 shelf waters, water temperature, residence time and the complexity of the biogeochemistry are major factors that govern the pCO2 in estuaries, but wind speed, seldom discussed, is critical to controlling the air–water exchanges of CO2. The total annual release of CO2 from the world's estuaries is now estimated to be 0.10 Pg C yr−1, which is much lower than published values mainly because of the contribution of a considerable amount of heretofore unpublished or new data from Asia and the Arctic. The Asian data, although indicating high pCO2, are low in sea-to-air fluxes because of low wind speeds. Previously determined flux values rely heavily on data from Europe and North America, where pCO2 is lower but wind speeds are much higher, such that the CO2 fluxes are higher than in Asia. Newly emerged CO2 flux data in the Arctic reveal that estuaries there mostly absorb rather than release CO2. Most continental shelves, and especially those at high latitude, are undersaturated in terms of CO2 and absorb CO2 from the

Using eddy covariance to measure the dependence of air-sea CO2 exchange rate on friction velocity

Science.gov (United States)

Landwehr, Sebastian; Miller, Scott D.; Smith, Murray J.; Bell, Thomas G.; Saltzman, Eric S.; Ward, Brian

2018-03-01

Parameterisation of the air-sea gas transfer velocity of CO2 and other trace gases under open-ocean conditions has been a focus of air-sea interaction research and is required for accurately determining ocean carbon uptake. Ships are the most widely used platform for air-sea flux measurements but the quality of the data can be compromised by airflow distortion and sensor cross-sensitivity effects. Recent improvements in the understanding of these effects have led to enhanced corrections to the shipboard eddy covariance (EC) measurements.Here, we present a revised analysis of eddy covariance measurements of air-sea CO2 and momentum fluxes from the Southern Ocean Surface Ocean Aerosol Production (SOAP) study. We show that it is possible to significantly reduce the scatter in the EC data and achieve consistency between measurements taken on station and with the ship underway. The gas transfer velocities from the EC measurements correlate better with the EC friction velocity (u*) than with mean wind speeds derived from shipboard measurements corrected with an airflow distortion model. For the observed range of wind speeds (u10 N = 3-23 m s-1), the transfer velocities can be parameterised with a linear fit to u*. The SOAP data are compared to previous gas transfer parameterisations using u10 N computed from the EC friction velocity with the drag coefficient from the Coupled Ocean-Atmosphere Response Experiment (COARE) model version 3.5. The SOAP results are consistent with previous gas transfer studies, but at high wind speeds they do not support the sharp increase in gas transfer associated with bubble-mediated transfer predicted by physically based models.

Turbulence structure and CO2 transfer at the air-sea interface and turbulent diffusion in thermally-stratified flows

International Nuclear Information System (INIS)

Komori, S.

1996-01-01

in clarifying environmental flow phenomena. This report summarizes research on two turbulence structure and diffusion topics; turbulence structure and the gas transfer mechanism across the air-sea (air-water) interface and the heat and momentum transfer mechanism in thermally stratified flows. The first study shows the relationship between the carbon dioxide (CO 2 ) transfer mechanism across a sheared air-water interface and the turbulence structure near the interface. The results revealed that the conventional proportional relationship between CO 2 transfer velocity across the air-sea interface and mean wind speed over the sea surface is incorrect. The second study numerically clarified the significant effects of molecular diffusivity (the Prandtl number) of active heat on heat transfer in stable thermally-stratified Hows. The results obtained from the two studies are described in the next two chapters. Since the results are mainly quoted from a series of previously published and in press works by Komori et al.'s research group (see references), this report might be considered as a summary of those works

Air-Sea CO2 fluxes in the Atlantic as measured during boreal spring and autumn

Directory of Open Access Journals (Sweden)

A. F. Ríos

2010-05-01

Full Text Available A total of fourteen hydrographic cruises from 2000 to 2008 were conducted during the spring and autumn seasons between Spain and the Southern Ocean under the framework of the Spanish research project FICARAM. The underway measurements were processed and analysed to describe the meridional air-sea CO2 fluxes (FCO2 in the covered sector of the Atlantic Ocean. The data has been grouped into different biogeochemical oceanographic provinces based on thermohaline characteristics. The spatial and temporal distributions of FCO2 followed expected distributions and annual trends reproducing the recent climatological ΔfCO2 estimations with a mean difference of −3 ± 18 μatm (Takahashi et al., 2009. The reduction in the CO2 saturation along the meridional FICARAM cruises represented an increase of 0.02 ± 0.14 mol m−2 yr−1 in the ocean uptake of atmospheric CO2. The subtropical waters in both Hemispheres acted as a sink of atmospheric CO2 during the successive spring seasons and as a source in autumn. The coarse reduction of the ocean uptake of atmospheric CO2 observed in the North Atlantic Ocean was linked to conditions of negative phase of the North Atlantic Oscillation that prevailed during the FICARAM period. Surface waters in the North Equatorial Counter Current revealed a significant long-term decrease of sea surface salinity of −0.16 ± 0.01 yr−1 coinciding with a declination of −3.5 ± 0.9 μatm yr−1 in the air–sea disequilibrium of CO2 fugacity and a rise of oceanic CO2 uptake of −0.09 ± 0.03 mol m−2 yr−1. The largest CO2 source was located in the equatorial upwelling system. These tropical waters that reached emissions of 0.7 ± 0.5 and 1.0 ± 0.7 mol m−2 y−1 in spring and autumn, respectively, showed an interannual warming of 0.11 ± 0.03 °C yr−1 and a wind speed decrease of −0.58 ± 0.14 m s−1 yr−1 in spring cruises which suggest the weakening of upwelling events associated with warm El Niño – Southern

The Role of Sea Ice in 2 x CO2 Climate Model Sensitivity. Part 2; Hemispheric Dependencies

Science.gov (United States)

Rind, D.; Healy, R.; Parkinson, C.; Martinson, D.

1997-01-01

How sensitive are doubled CO2 simulations to GCM control-run sea ice thickness and extent? This issue is examined in a series of 10 control-run simulations with different sea ice and corresponding doubled CO2 simulations. Results show that with increased control-run sea ice coverage in the Southern Hemisphere, temperature sensitivity with climate change is enhanced, while there is little effect on temperature sensitivity of (reasonable) variations in control-run sea ice thickness. In the Northern Hemisphere the situation is reversed: sea ice thickness is the key parameter, while (reasonable) variations in control-run sea ice coverage are of less importance. In both cases, the quantity of sea ice that can be removed in the warmer climate is the determining factor. Overall, the Southern Hemisphere sea ice coverage change had a larger impact on global temperature, because Northern Hemisphere sea ice was sufficiently thick to limit its response to doubled CO2, and sea ice changes generally occurred at higher latitudes, reducing the sea ice-albedo feedback. In both these experiments and earlier ones in which sea ice was not allowed to change, the model displayed a sensitivity of -0.02 C global warming per percent change in Southern Hemisphere sea ice coverage.

Co-benefits of global and regional greenhouse gas mitigation for US air quality in 2050

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yuqiang; Bowden, Jared H.; Adelman, Zachariah; Naik, Vaishali; Horowitz, Larry W.; Smith, Steven J.; West, J. Jason

2016-08-01

Policies to mitigate greenhouse gas (GHG) emissions will not only slow climate change but can also have ancillary benefits of improved air quality. Here we examine the co-benefits of both global and regional GHG mitigation for US air quality in 2050 at fine resolution, using dynamical downscaling methods, building on a previous global co-benefits study (West et al., 2013). The co-benefits for US air quality are quantified via two mechanisms: through reductions in co-emitted air pollutants from the same sources and by slowing climate change and its influence on air quality, following West et al. (2013). Additionally, we separate the total co-benefits into contributions from domestic GHG mitigation vs. mitigation in foreign countries. We use the Weather Research and Forecasting (WRF) model to dynamically downscale future global climate to the regional scale and the Sparse Matrix Operator Kernel Emissions (SMOKE) program to directly process global anthropogenic emissions to the regional domain, and we provide dynamical boundary conditions from global simulations to the regional Community Multi-scale Air Quality (CMAQ) model. The total co-benefits of global GHG mitigation from the RCP4.5 scenario compared with its reference are estimated to be higher in the eastern US (ranging from 0.6 to 1.0 µg m^-3) than the west (0–0.4 µg m^-3) for fine particulate matter (PM_2.5), with an average of 0.47 µg m^-3 over the US; for O₃, the total co-benefits are more uniform at 2–5 ppb, with a US average of 3.55 ppb. Comparing the two mechanisms of co-benefits, we find that reductions in co-emitted air pollutants have a much greater influence on both PM_2.5 (96 % of the total co-benefits) and O₃ (89 % of the total) than the second co-benefits mechanism via slowing climate change, consistent with West et al. (2013). GHG mitigation from foreign countries contributes more to the US O₃ reduction

Contribution of tropical cyclones to the air-sea CO2 flux: A global view

Digital Repository Service at National Institute of Oceanography (India)

Levy, M.; Lengaigne, M.; Bopp, L.; Vincent, E.M.; Madec, G.; Ethe, C.; DileepKumar, M.; Sarma, V.V.S.S.

.ocemod.2006.11.003.501 D’Asaro, E. (2003), The ocean boundary layer below hurricane dennis, Journal of physical502 oceanography, 33(3), 561–579.503 D’Asaro,E.,andC.McNeil(2007),Air-seagasexchangeatextremewindspeedsmeasured504 by autonomous oceanographic floats... at high wind speed [Liss and Merlivat, 1986; Wanninkhof, 1992; D’Asaro and McNeil,55 2007; McNeil and D’Asaro, 2007]. TCs also impact F CO 2 because their intense surface56 winds increase vertical entrainment of subsurface waters (hereafter referred...

ISLSCP II Air-Sea Carbon Dioxide Gas Exchange

Data.gov (United States)

National Aeronautics and Space Administration — This data set contains the calculated net ocean-air carbon dioxide (CO2) flux and sea-air CO2 partial pressure (pCO2) difference. The estimates are based on...

Relationship between sea level and climate forcing by CO2 on geological timescales.

Science.gov (United States)

Foster, Gavin L; Rohling, Eelco J

2013-01-22

On 10(3)- to 10(6)-year timescales, global sea level is determined largely by the volume of ice stored on land, which in turn largely reflects the thermal state of the Earth system. Here we use observations from five well-studied time slices covering the last 40 My to identify a well-defined and clearly sigmoidal relationship between atmospheric CO(2) and sea level on geological (near-equilibrium) timescales. This strongly supports the dominant role of CO(2) in determining Earth's climate on these timescales and suggests that other variables that influence long-term global climate (e.g., topography, ocean circulation) play a secondary role. The relationship between CO(2) and sea level we describe portrays the "likely" (68% probability) long-term sea-level response after Earth system adjustment over many centuries. Because it appears largely independent of other boundary condition changes, it also may provide useful long-range predictions of future sea level. For instance, with CO(2) stabilized at 400-450 ppm (as required for the frequently quoted "acceptable warming" of 2 °C), or even at AD 2011 levels of 392 ppm, we infer a likely (68% confidence) long-term sea-level rise of more than 9 m above the present. Therefore, our results imply that to avoid significantly elevated sea level in the long term, atmospheric CO(2) should be reduced to levels similar to those of preindustrial times.

Carbon dynamics and CO2 air-sea exchanges in the eutrophied coastal waters of the Southern Bight of the North Sea: a modelling study

Directory of Open Access Journals (Sweden)

N. Gypens

2004-01-01

Full Text Available A description of the carbonate system has been incorporated in the MIRO biogeochemical model to investigate the contribution of diatom and Phaeocystis blooms to the seasonal dynamics of air-sea CO2 exchanges in the Eastern Channel and Southern Bight of the North Sea, with focus on the eutrophied Belgian coastal waters. For this application, the model was implemented in a simplified three-box representation of the hydrodynamics with the open ocean boundary box ‘Western English Channel’ (WCH and the ‘French Coastal Zone’ (FCZ and ‘Belgian Coastal Zone’ (BCZ boxes receiving carbon and nutrients from the rivers Seine and Scheldt, respectively. Results were obtained by running the model for the 1996–1999 period. The simulated partial pressures of CO2 (pCO2 were successfully compared with data recorded over the same period in the central BCZ at station 330 (51°26.05′ N; 002°48.50′ E. Budget calculations based on model simulations of carbon flow rates indicated for BCZ a low annual sink of atmospheric CO2 (−0.17 mol C m-2 y-1. On the opposite, surface water pCO2 in WCH was estimated to be at annual equilibrium with respect to atmospheric CO2. The relative contribution of biological, chemical and physical processes to the modelled seasonal variability of pCO2 in BCZ was further explored by running model scenarios with separate closures of biological activities and/or river inputs of carbon. The suppression of biological processes reversed direction of the CO2 flux in BCZ that became, on an annual scale, a significant source for atmospheric CO2 (+0.53 mol C m-2 y-1. Overall biological activity had a stronger influence on the modelled seasonal cycle of pCO2 than temperature. Especially Phaeocystis colonies which growth in spring were associated with an important sink of atmospheric CO2 that counteracted the temperature-driven increase of pCO2 at this period of the year. However, river inputs of organic and inorganic carbon were

Air–Sea CO2 Gas Transfer Velocity in a Shallow Estuary

DEFF Research Database (Denmark)

Mørk, Eva Thorborg; Sørensen, Lise Lotte; Jensen, Bjarne

2014-01-01

The air–sea transfer velocity of CO2(kCO2) was investigated in a shallow estuary in March to July 2012, using eddy-covariance measurements of CO2 fluxes and measured air–sea CO2 partial-pressure differences. A data evaluation method that eliminates data by nine rejection criteria in order......, the transfer velocity in the shallow water estuary was lower than in other coastal waters, possibly a symptom of low tidal amplitude leading to low intensity water turbulence. High transfer velocities were recorded above wind speeds of 5 m s−1 , believed to be caused by early-breaking waves and the large fetch...... (6.5 km) of the estuary. These findings indicate that turbulence in both air and water influences the transfer velocity....

Carbon isotope evidence for the latitudinal distribution and wind speed dependence of the air-sea gas transfer velocity

International Nuclear Information System (INIS)

Krakauer, Nir Y.

2006-01-01

The air-sea gas transfer velocity is an important determinant of the exchange of gases, including CO 2 , between the atmosphere and ocean, but the magnitude of the transfer velocity and what factors control it remains poorly known. Here, we use oceanic and atmospheric observations of 14 C and 13 C to constrain the global mean gas transfer velocity as well as the exponent of its wind speed dependence, utilizing the distinct signatures left by the air-sea exchange of 14 CO 2 and 13 CO 2 . While the atmosphere and ocean inventories of 14 CO 2 and 13 CO 2 constrain the mean gas transfer velocity, the latitudinal pattern in the atmospheric and oceanic 14 C and 13 C distributions contain information about the wind speed dependence. We computed the uptake of bomb 14 C by the ocean for different transfer velocity patterns using pulse response functions from an ocean general circulation model, and evaluated the match between the predicted bomb 14 C concentrations and observationally based estimates for the 1970s-1990s. Using a wind speed climatology based on satellite measurements, we solved either for the best-fit global relationship between gas exchange and mean wind speed or for the mean gas transfer velocity over each of 11 ocean regions. We also compared the predicted consequences of different gas exchange relationships on the rate of change and interhemisphere gradient of 14 C in atmospheric CO 2 with tree-ring and atmospheric measurements. Our results suggest that globally, the dependence of the air-sea gas transfer velocity on wind speed is close to linear, with an exponent of 0.5 ± 0.4, and that the global mean gas transfer velocity at a Schmidt number of 660 is 20 ± 3 cm/hr, similar to the results of previous analyses. We find that the air-sea flux of 13 C estimated from atmosphere and ocean observations also suggests a lower than quadratic dependence of gas exchange on wind speed

On which timescales do gas transfer velocities control North Atlantic CO2 flux variability?

OpenAIRE

Couldrey, Matthew; Oliver, Kevin; Yool, Andrew; Halloran, Paul; Achterberg, Eric

2016-01-01

The North Atlantic is an important basin for the global ocean's uptake of anthropogenic and natural carbon dioxide (CO2), but the mechanisms controlling this carbon flux are not fully understood. The air-sea flux of CO2, F, is the product of a gas transfer velocity, k, the air-sea CO2 concentration gradient, ΔpCO2, and the temperature and salinity-dependent solubility coefficient, α. k is difficult to constrain, representing the dominant uncertainty in F on short (instantaneous to interannual...

The idea of global CO2 trade

International Nuclear Information System (INIS)

Svendsen, G.T.

1999-01-01

The US has been criticized for wanting to earn a fortune on a global CO 2 market. However, compared to the situation without trade and provided that such a market is designed so that it does not pay to cheat, a global CO 2 market may provide the world with an epoch-making means of cost-effective control which can solve future global environmental problems. The economic gains from 'hot air' distributions of permits and CO 2 trade make the system politically attractive to potential participants. For example, vital financial subsidies from the EU to Eastern Europe are to be expected. It will probably not pay to cheat if quotas are renewed periodically by the UN. Cheating countries are then to be excluded from further profitable trade. Also, a periodical renewal of permits makes it possible to tighten target levels in the future

Simulated anthropogenic CO2 storage and acidification of the Mediterranean Sea

Directory of Open Access Journals (Sweden)

J. Palmiéri

2015-02-01

Full Text Available Constraints on the Mediterranean Sea's storage of anthropogenic CO2 are limited, coming only from data-based approaches that disagree by more than a factor of two. Here we simulate this marginal sea's anthropogenic carbon storage by applying a perturbation approach in a high-resolution regional model. Our model simulates that, between 1800 and 2001, basin-wide CO2 storage by the Mediterranean Sea has increased by 1.0 Pg C, a lower limit based on the model's weak deep-water ventilation, as revealed by evaluation with CFC-12. Furthermore, by testing a data-based approach (transit time distribution in our model, comparing simulated anthropogenic CO2 to values computed from simulated CFC-12 and physical variables, we conclude that the associated basin-wide storage of 1.7 Pg, published previously, must be an upper bound. Out of the total simulated storage of 1.0 Pg C, 75% comes from the air–sea flux into the Mediterranean Sea and 25% comes from net transport from the Atlantic across the Strait of Gibraltar. Sensitivity tests indicate that the Mediterranean Sea's higher total alkalinity, relative to the global-ocean mean, enhances the Mediterranean's total inventory of anthropogenic carbon by 10%. Yet the corresponding average anthropogenic change in surface pH does not differ significantly from the global-ocean average, despite higher total alkalinity. In Mediterranean deep waters, the pH change is estimated to be between −0.005 and −0.06 pH units.

Elevated CO2 stimulates marsh elevation gain, counterbalancing sea-level rise.

Science.gov (United States)

Langley, J Adam; McKee, Karen L; Cahoon, Donald R; Cherry, Julia A; Megonigal, J Patrick

2009-04-14

Tidal wetlands experiencing increased rates of sea-level rise (SLR) must increase rates of soil elevation gain to avoid permanent conversion to open water. The maximal rate of SLR that these ecosystems can tolerate depends partly on mineral sediment deposition, but the accumulation of organic matter is equally important for many wetlands. Plant productivity drives organic matter dynamics and is sensitive to global change factors, such as rising atmospheric CO(2) concentration. It remains unknown how global change will influence organic mechanisms that determine future tidal wetland viability. Here, we present experimental evidence that plant response to elevated atmospheric [CO(2)] stimulates biogenic mechanisms of elevation gain in a brackish marsh. Elevated CO(2) (ambient + 340 ppm) accelerated soil elevation gain by 3.9 mm yr(-1) in this 2-year field study, an effect mediated by stimulation of below-ground plant productivity. Further, a companion greenhouse experiment revealed that the CO(2) effect was enhanced under salinity and flooding conditions likely to accompany future SLR. Our results indicate that by stimulating biogenic contributions to marsh elevation, increases in the greenhouse gas, CO(2), may paradoxically aid some coastal wetlands in counterbalancing rising seas.

Elevated CO2 stimulates marsh elevation gain, counterbalancing sea-level rise

Science.gov (United States)

Langley, J. Adam; McKee, Karen L.; Cahoon, Donald R.; Cherry, Julia A.; Megonigal, J. Patrick

2009-01-01

Tidal wetlands experiencing increased rates of sea-level rise (SLR) must increase rates of soil elevation gain to avoid permanent conversion to open water. The maximal rate of SLR that these ecosystems can tolerate depends partly on mineral sediment deposition, but the accumulation of organic matter is equally important for many wetlands. Plant productivity drives organic matter dynamics and is sensitive to global change factors, such as rising atmospheric CO2 concentration. It remains unknown how global change will influence organic mechanisms that determine future tidal wetland viability. Here, we present experimental evidence that plant response to elevated atmospheric [CO2] stimulates biogenic mechanisms of elevation gain in a brackish marsh. Elevated CO2 (ambient + 340 ppm) accelerated soil elevation gain by 3.9 mm yr−1 in this 2-year field study, an effect mediated by stimulation of below-ground plant productivity. Further, a companion greenhouse experiment revealed that the CO2 effect was enhanced under salinity and flooding conditions likely to accompany future SLR. Our results indicate that by stimulating biogenic contributions to marsh elevation, increases in the greenhouse gas, CO2, may paradoxically aid some coastal wetlands in counterbalancing rising seas. PMID:19325121

Subsurface low pH and carbonate saturation state of aragonite on China side of the North Yellow Sea: combined effects of global atmospheric CO2 increase, regional environmental changes, and local biogeochemical processes

Science.gov (United States)

Zhai, W.-D.; Zheng, N.; Huo, C.; Xu, Y.; Zhao, H.-D.; Li, Y.-W.; Zang, K.-P.; Wang, J.-Y.; Xu, X.-M.

2013-02-01

Based upon seven field surveys conducted between May 2011 and January 2012, we investigated pH, carbonate saturation state of aragonite (Ωarag), and ancillary parameters on the Chinese side of the North Yellow Sea, a western North Pacific continental margin of major economic importance. Subsurface waters were nearly in equilibrium with air in May and June. From July to October, the fugacity of CO2 (fCO2) of bottom water gradually increased to 697 ± 103 μatm and pH decreased to 7.83 ± 0.07 due to respiration/remineralization processes of primary production induced biogenic particles. In November and January, bottom water fCO2 decreased and pH gradually returned to an air-equilibrated level due to cooling enhanced vertical mixing. The corresponding bottom water Ωarag was 1.74 ± 0.17 (May), 1.77 ± 0.26 (June), 1.70 ± 0.26 (July), 1.72 ± 0.33 (August), 1.32 ± 0.31 (October), 1.50 ± 0.28 (November), and 1.41 ± 0.12 (January). Critically low Ωarag values of 1.0 to 1.2 were mainly observed in subsurface waters in a salinity range of 31.5-32.5 psu in October and November, accounting for ~ 10% of the North Yellow Sea area. Water mass derived from the adjacent Bohai Sea had a typical water salinity of 30.5-31.5 psu, and bottom water Ωarag values ranged mostly between 1.6 and 2.4. This study showed that the carbonate system in the North Yellow Sea was substantially influenced by global atmospheric CO2 increase. The community respiration/remineralization rates in typical North Yellow Sea bottom water mass were estimated at 0.55-1.0 μmol O2 kg-1 d-1 in warm seasons, leading to seasonal drops in subsurface pH and Ωarag. Outflow of the Bohai Sea water mass counteracted the subsurface Ωarag reduction in the North Yellow Sea.

Ikaite crystal distribution in Arctic winter sea ice and implications for CO2 system dynamics

Science.gov (United States)

Rysgaard, S.; Søgaard, D. H.; Cooper, M.; Pućko, M.; Lennert, K.; Papakyriakou, T. N.; Wang, F.; Geilfus, N. X.; Glud, R. N.; Ehn, J.; McGinnnis, D. F.; Attard, K.; Sievers, J.; Deming, J. W.; Barber, D.

2012-12-01

The precipitation of ikaite (CaCO3·6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few µm to 700 µm were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea-ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surfaceice values of 700-900 µmol kg-1 ice (~ 25 × 106 crystals kg-1) to bottom-layer values of 100-200 µmol kg-1 ice (1-7 × 106 kg-1), all of which are much higher (4-10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration whereas TA concentrations in bottom layers were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolved in bottom layers. From these findings and model calculations we relate sea ice formation and melt to observed pCO2 conditions in polar surface waters, and hence, the air-sea CO2 flux.

Statistical analysis of global surface air temperature and sea level using cointegration methods

DEFF Research Database (Denmark)

Schmith, Torben; Johansen, Søren; Thejll, Peter

Global sea levels are rising which is widely understood as a consequence of thermal expansion and melting of glaciers and land-based ice caps. Due to physically-based models being unable to simulate observed sea level trends, semi-empirical models have been applied as an alternative for projecting...... of future sea levels. There is in this, however, potential pitfalls due to the trending nature of the time series. We apply a statistical method called cointegration analysis to observed global sea level and surface air temperature, capable of handling such peculiarities. We find a relationship between sea...... level and temperature and find that temperature causally depends on the sea level, which can be understood as a consequence of the large heat capacity of the ocean. We further find that the warming episode in the 1940s is exceptional in the sense that sea level and warming deviates from the expected...

The Idea of Global CO2 Trade

DEFF Research Database (Denmark)

Svendsen, Gert Tinggaard

1999-01-01

-effective control which can solve future global environmental problems. The economic gains from 'hot air' distributions of permits and CO2 trade make the system politically attractive to potential participants. For example, vital financial subsidies from the EU to Eastern Europe are to be expected. It will probably...

A generalized model for the air-sea transfer of dimethyl sulfide at high wind speeds

Science.gov (United States)

Vlahos, Penny; Monahan, Edward C.

2009-11-01

The air-sea exchange of dimethyl sulfide (DMS) is an important component of ocean biogeochemistry and global climate models. Both laboratory experiments and field measurements of DMS transfer rates have shown that the air-sea flux of DMS is analogous to that of other significant greenhouse gases such as CO2 at low wind speeds (10 m/s. The result is an attenuation of the dimensionless Henry's Law constant (H) where (Heff = H/(1 + (Cmix/Cw) ΦB) by a solubility enhancement Cmix/Cw, and the fraction of bubble surface area per m2 surface ocean.

The global climatology of an interannually varying air-sea flux data set

Energy Technology Data Exchange (ETDEWEB)

Large, W.G.; Yeager, S.G. [National Center for Atmospheric Research, Boulder, CO (United States)

2009-08-15

The air-sea fluxes of momentum, heat, freshwater and their components have been computed globally from 1948 at frequencies ranging from 6-hourly to monthly. All fluxes are computed over the 23 years from 1984 to 2006, but radiation prior to 1984 and precipitation before 1979 are given only as climatological mean annual cycles. The input data are based on NCEP reanalysis only for the near surface vector wind, temperature, specific humidity and density, and on a variety of satellite based radiation, sea surface temperature, sea-ice concentration and precipitation products. Some of these data are adjusted to agree in the mean with a variety of more reliable satellite and in situ measurements, that themselves are either too short a duration, or too regional in coverage. The major adjustments are a general increase in wind speed, decrease in humidity and reduction in tropical solar radiation. The climatological global mean air-sea heat and freshwater fluxes (1984-2006) then become 2 W/m{sup 2} and -0.1 mg/m{sup 2} per second, respectively, down from 30 W/m{sup 2} and 3.4 mg/m{sup 2} per second for the unaltered data. However, decadal means vary from 7.3 W/m{sup 2} (1977-1986) to -0.3 W/m{sup 2} (1997-2006). The spatial distributions of climatological fluxes display all the expected features. A comparison of zonally averaged wind stress components across ocean sub-basins reveals large differences between available products due both to winds and to the stress calculation. Regional comparisons of the heat and freshwater fluxes reveal an alarming range among alternatives; typically 40 W/m{sup 2} and 10 mg/m{sup 2} per second, respectively. The implied ocean heat transports are within the uncertainty of estimates from ocean observations in both the Atlantic and Indo-Pacific basins. They show about 2.4 PW of tropical heating, of which 80% is transported to the north, mostly in the Atlantic. There is similar good agreement in freshwater transport at many latitudes in both

A multi-model assessment of the co-benefits of climate mitigation for global air quality

Energy Technology Data Exchange (ETDEWEB)

Rao, Shilpa; Klimont, Zbigniew; Leitao, Joana; Riahi, Keywan; van Dingenen, Rita; Reis, Lara Aleluia; Calvin, Katherine; Dentener, Frank; Drouet, Laurent; Fujimori, Shinichiro; Harmsen, Mathijs; Luderer, Gunnar; Heyes, Chris; Strefler, Jessica; Tavoni, Massimo; van Vuuren, Detlef P.

2016-12-01

The recent International Panel on Climate change (IPCC) report identifies significant co-benefits from climate policies on near-term ambient air pollution and related human health outcomes [1]. This is increasingly relevant for policy making as the health impacts of air pollution are a major global concern- the Global Burden of Disease (GBD) study identifies outdoor air pollution as the sixth major cause of death globally [2]. Integrated assessment models (IAMs) are an effective tool to evaluate future air pollution outcomes across a wide range of assumptions on socio-economic development and policy regimes. The Representative Concentration Pathways (RCPs) [3] were the first set of long-term global scenarios developed across multiple integrated assessment models that provided detailed estimates of a number of air pollutants until 2100. However these scenarios were primarily designed to cover a defined range of radiative forcing outcomes and thus did not specifically focus on the interactions of long-term climate goals on near-term air pollution impacts. More recently, [4] used the RCP4.5 scenario to evaluate the co-benefits of global GHG reductions on air quality and human health in 2030. [5-7] have further examined the interactions of more diverse pollution control regimes with climate policies. This paper extends the listed studies in a number of ways. Firstly it uses multiple IAMs to look into the co-benefits of a global climate policy for ambient air pollution under harmonized assumptions on near-term air pollution control. Multi-model frameworks have been extensively used in the analysis of climate change mitigation pathways, and the structural uncertainties regarding the underlying mechanisms (see for example [8-10]. This is to our knowledge the first time that a multi-model evaluation has been specifically designed and applied to analyze the co-benefits of climate change policy on ambient air quality, thus enabling a better understanding of at a detailed

Global warming: Sea ice and snow cover

International Nuclear Information System (INIS)

Walsh, J.E.

1993-01-01

In spite of differences among global climate simulations under scenarios where atmospheric CO 2 is doubled, all models indicate at least some amplification of greenouse warming at the polar regions. Several decades of recent data on air temperature, sea ice, and snow cover of the high latitudes of the Northern Hemisphere are summarized to illustrate the general compatibility of recent variations in those parameters. Despite a data void over the Arctic Ocean, some noteworthy patterns emerge. Warming dominates in winter and spring, as projected by global climate models, with the warming strongest over subpolar land areas of Alaska, northwestern Canada, and northern Eurasia. A time-longitude summary of Arctic sea ice variations indicates that timescales of most anomalies range from several months to several years. Wintertime maxima of total sea ice extent contain no apparent secular trends. The statistical significance of trends in recent sea ice variations was evaluated by a Monte Carlo procedure, showing a statistically significant negative trend in the summer. Snow cover data over the 20-y period of record show a noticeable decrease of Arctic snow cover in the late 1980s. This is of potential climatic significance since the accompanying decrease of surface albedo leads to a rapid increase of solar heating. 21 refs., 3 figs., 1 tab

Acceleration of modern acidification in the South China Sea driven by anthropogenic CO2

Science.gov (United States)

Liu, Yi; Peng, Zicheng; Zhou, Renjun; Song, Shaohua; Liu, Weiguo; You, Chen-Feng; Lin, Yen-Po; Yu, Kefu; Wu, Chung-Che; Wei, Gangjian; Xie, Luhua; Burr, George S.; Shen, Chuan-Chou

2014-01-01

Modern acidification by the uptake of anthropogenic CO2 can profoundly affect the physiology of marine organisms and the structure of ocean ecosystems. Centennial-scale global and regional influences of anthropogenic CO2 remain largely unknown due to limited instrumental pH records. Here we present coral boron isotope-inferred pH records for two periods from the South China Sea: AD 1048–1079 and AD 1838–2001. There are no significant pH differences between the first period at the Medieval Warm Period and AD 1830–1870. However, we find anomalous and unprecedented acidification during the 20th century, pacing the observed increase in atmospheric CO2. Moreover, pH value also varies in phase with inter-decadal changes in Asian Winter Monsoon intensity. As the level of atmospheric CO2 keeps rising, the coupling global warming via weakening the winter monsoon intensity could exacerbate acidification of the South China Sea and threaten this expansive shallow water marine ecosystem. PMID:24888785

Sensitivity Analysis for Atmospheric Infrared Sounder (AIRS) CO2 Retrieval

Science.gov (United States)

Gat, Ilana

2012-01-01

The Atmospheric Infrared Sounder (AIRS) is a thermal infrared sensor able to retrieve the daily atmospheric state globally for clear as well as partially cloudy field-of-views. The AIRS spectrometer has 2378 channels sensing from 15.4 micrometers to 3.7 micrometers, of which a small subset in the 15 micrometers region has been selected, to date, for CO2 retrieval. To improve upon the current retrieval method, we extended the retrieval calculations to include a prior estimate component and developed a channel ranking system to optimize the channels and number of channels used. The channel ranking system uses a mathematical formalism to rapidly process and assess the retrieval potential of large numbers of channels. Implementing this system, we identifed a larger optimized subset of AIRS channels that can decrease retrieval errors and minimize the overall sensitivity to other iridescent contributors, such as water vapor, ozone, and atmospheric temperature. This methodology selects channels globally by accounting for the latitudinal, longitudinal, and seasonal dependencies of the subset. The new methodology increases accuracy in AIRS CO2 as well as other retrievals and enables the extension of retrieved CO2 vertical profiles to altitudes ranging from the lower troposphere to upper stratosphere. The extended retrieval method for CO2 vertical profile estimation using a maximum-likelihood estimation method. We use model data to demonstrate the beneficial impact of the extended retrieval method using the new channel ranking system on CO2 retrieval.

Evaluation of the alkalinity in sea water by means of gran calculation. A procedure for titration in order to quantify the acidification of the seas by CO{sub 2} absorption; Bestimmung der Alkalinitaet in Meerwasser durch Granberechnung. Ein Titrationsverfahren zur Quantifizierung der Versauerung der Meere durch CO{sub 2}-Aufnahme

Energy Technology Data Exchange (ETDEWEB)

Peters, Juergen [SI Analytics GmbH, Mainz (Germany)

2012-04-15

In the last 200 years, the content of carbon dioxide in the air has risen from about 280 ppm to more than 380 ppm. Here, the increase of the concentration of CO{sub 2} is discussed as a reason for 'global warming'. While in the atmosphere about 800 billion tons of carbon dioxide (calculated as carbon) are located, 38,000 billion tons of carbon dioxide are dissolved in seawater, ie 50 times of the amount of CO{sub 2} in the atmosphere. The increase in the amount of CO{sub 2} in the atmosphere also results in an almost 50-fold increase in the total dissolved carbon dioxide in the sea. This results in a lowering of the pH value, and in an influencing of the equilibrium of aragonite and calcite. Many sea creatures are hampered in their growth.

Interannual variations of net community production and air-sea CO2 flux from winter to spring in the western subarctic North Pacific

International Nuclear Information System (INIS)

Midorikawa, Takashi; Ogawa, Kan; Nemoto, Kazuhiro; Kamiya, Hitomi; Umeda, Takafumi; Hiraishi, Naotaka; Wada, Akira; Ishii, Masao

2003-01-01

The role of spring biological production for the air-sea CO 2 flux was quantified in the Western Subarctic Gyre (48 deg N, 165 deg E), where the vertical profile of temperature revealed the existence of a temperature minimum (Tmin) layer in the North Pacific. The vertical profiles of temperature, salinity, dissolved oxygen, nutrients and dissolved inorganic carbon, DIC, in the upper water column were significantly variable year by year in spring, 1996-2000. Correspondingly, surface seawater at this site in spring was supersaturated with CO 2 in 1997, 1999 and 2000, but was undersaturated in 1996 and 1998. The concentrations of DIC and nutrients in the winter mixed layer were estimated from those in the Tmin layer in spring with a correction for particle decomposition based on the apparent oxygen utilization. The net community production (NCP) and air-sea CO 2 flux from winter to spring were calculated from the vertically integrated deficits of DIC and nutrients in the upper water column between the two seasons. The calculation of the carbon budget indicated large interannual variations of NCP (0-13 mmol/m 2 /d) and CO 2 efflux (4-16 mmol/m 2 /d) for this period. The CO 2 efflux was generally low in the year when NCP was high. The close coupling between biological production and CO 2 efflux suggested the important role of the changes in the mixed-layer depth, as a key process controlling both processes, especially of the timing, so that a decrease in the mixed-layer depth could result in the activation of biological production. The early biological consumption of the surface DIC concentration could shorten the period for acting as a source for atmospheric CO 2 and depress the CO 2 efflux in the Western Subarctic Gyre from winter to spring in 1996 and 1998. On the contrary, in 1997, persistently deep vertical mixing until late spring could suppress the biological activity and give rise to long-lasting CO 2 efflux

Energy and material balance of CO2 capture from ambient air.

Science.gov (United States)

Zeman, Frank

2007-11-01

Current Carbon Capture and Storage (CCS) technologies focus on large, stationary sources that produce approximately 50% of global CO2 emissions. We propose an industrial technology that captures CO2 directly from ambient air to target the remaining emissions. First, a wet scrubbing technique absorbs CO2 into a sodium hydroxide solution. The resultant carbonate is transferred from sodium ions to calcium ions via causticization. The captured CO2 is released from the calcium carbonate through thermal calcination in a modified kiln. The energy consumption is calculated as 350 kJ/mol of CO2 captured. It is dominated by the thermal energy demand of the kiln and the mechanical power required for air movement. The low concentration of CO2 in air requires a throughput of 3 million cubic meters of air per ton of CO2 removed, which could result in significant water losses. Electricity consumption in the process results in CO2 emissions and the use of coal power would significantly reduce to net amount captured. The thermodynamic efficiency of this process is low but comparable to other "end of pipe" capture technologies. As another carbon mitigation technology, air capture could allow for the continued use of liquid hydrocarbon fuels in the transportation sector.

Evidence from the Baltic Sea for an enhanced CO{sub 2} air-sea transfer velocity

Energy Technology Data Exchange (ETDEWEB)

Kuss, Joachim; Nagel, Klaus; Schneider, Bernd [Baltic Sea Research Institute, Warnemuende (Germany). Dept. of Marine Chemistry

2004-04-01

Surface water total CO{sub 2} concentrations (CT) and the CO{sub 2} partial pressure of the surface water and in the atmosphere were measured in the eastern Gotland Sea at approximately monthly intervals during five cruises in the winter of 1999/2000. Taking into account vertical/lateral exchange processes and the decomposition of organic matter, the monthly changes in CT were used to determine CO{sub 2} evasion fluxes. In addition, the CO{sub 2} fluxes were calculated on the basis of the CO{sub 2} partial pressure differences using local wind speed (u) records and different currently applied parametrizations of the gas exchange transfer velocity (k). The latter resulted in substantially lower monthly fluxes that indicated a considerable underestimation of k from the k(u) functions used. To achieve an optimal agreement between the flux calculations and the balance-derived CO{sub 2} fluxes, the coefficients of both a simple quadratic and cubic function k(u) were iterated using a least-squares fitting procedure. The resulting equations, which refer to short-term wind data and to the CO{sub 2} exchange at 20 deg C, were k= (0.45 {+-} 0.10)u{sup 2} and k(0.037 {+-} 0.008)u{sup 3} (k, cm/h; u, m/s) . These yielded higher k values than most of the previously proposed parametrizations. Unfortunately, our data did not allow us to decide whether the quadratic or cubic function is more appropriate to describe the gas exchange dynamics.

Air-Sea Interaction

Science.gov (United States)

Csanady, G. T.

2001-03-01

In recent years air-sea interaction has emerged as a subject in its own right, encompassing small-scale and large-scale processes in both air and sea. Air-Sea Interaction: Laws and Mechanisms is a comprehensive account of how the atmosphere and the ocean interact to control the global climate, what physical laws govern this interaction, and its prominent mechanisms. The topics covered range from evaporation in the oceans, to hurricanes, and on to poleward heat transport by the oceans. By developing the subject from basic physical (thermodynamic) principles, the book is accessible to graduate students and research scientists in meteorology, oceanography, and environmental engineering. It will also be of interest to the broader physics community involved in the treatment of transfer laws, and thermodynamics of the atmosphere and ocean.

Ikaite crystals in melting sea ice - implications for pCO2 and pH levels in Arctic surface waters

Science.gov (United States)

Rysgaard, S.; Glud, R. N.; Lennert, K.; Cooper, M.; Halden, N.; Leakey, R. J. G.; Hawthorne, F. C.; Barber, D.

2012-08-01

A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air-sea CO2 exchange. This has been complicated by the recent discoveries of ikaite (a polymorph of CaCO3·6H2O) in Arctic and Antarctic sea ice, which indicate that multiple chemical transformations occur in sea ice with a possible effect on CO2 and pH conditions in surface waters. Here, we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from a melting 1.7 km2 (0.5-1 m thick) drifting ice floe in the Fram Strait during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice floe thickness by 0.2 m per week and resulted in an estimated 3.8 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air-sea CO2 uptake of 10.6 mmol m-2 sea ice d-1 or to 3.3 ton km-2 ice floe week-1. This is markedly higher than the estimated primary production within the ice floe of 0.3-1.3 mmol m-2 sea ice d-1. Finally, the presence of ikaite in sea ice and the dissolution of the mineral during melting of the sea ice and mixing of the melt water into the surface oceanic mixed layer accounted for half of the estimated pCO2 uptake.

Climatic significance of stable isotope characteristics of air-CO2 and rainfall in Delhi area water-plant-air system

International Nuclear Information System (INIS)

Datta, P.S.; Tyagi, S.K.

2002-01-01

In recent years, there is a global concern on the role of carbon dioxide in atmosphere in affecting the climate. The present models of global atmospheric circulation suggest that oceans sequester about one-third of the CO 2 released by anthropogenic activities, and biospheric productivity is the primary cause of the interannual fluctuations in the atmospheric CO 2 . However, most of the times, the excess of CO 2 in air is associated with the presence of anthropogenic pollutants from urbanised centres. Therefore, the studies on the pattern of local variations in the isotopic composition of air CO 2 and rainfall in urban areas are expected to provide important information on the atmospheric circulation processes which affect the climate on a regional scale. Internationally, aspects of climate change have been so far demonstrated using isotopic data mainly from temperate climates, and there is limited understanding of the factors controlling stable isotopic composition of air-CO 2 and rainfall in tropical regions. In this context, to assess the magnitude of the above mentioned effects, analysis of the data on the variations in the 13 C/ 12 C and 18 O/ 16 O signatures of air-CO 2 in Delhi area water-plant-air system is presented here

Air pollution related to sea transport

International Nuclear Information System (INIS)

Massin, J.M.; Hertz, O.

1993-01-01

Sea transportation contributes only 1-2% of world CO 2 emissions. Owing to the sulphur concentration in the bunker fuels, this transportation mode represents over 4% of the world SO 2 emissions. In addition, NO x emissions are likely to exceed 7% of the world emissions. SO 2 emissions in the North Sea and the Channel account for 15% of the whole French emissions, NO x emissions for about 10% and CO 2 emissions for about 3%. There are several potential measures to reduce the emissions of ship engines - propelling engines or generator driving engines - improvement of fuel quality, by desulphurizing and prohibiting the use of noxious additives such as PCB; use of alternative fuels; engine optimizing; exhaust gas processing; use of new propelling systems. A new organisation of world marketing of fuels with low or high sulphur levels could also be set up. The Sea Protection Committee of the International Maritime Organisation (IMO) discussed this problem during its meeting in 1990. The 73/78 MARPOL convention provides the IMO with an international juridical tool, especially designed for the preclusion of pollution due to sea transportation. It can address the issue of air pollution which requires a concerted approach between seaside countries and the drawing up of international regulations relating to the protection of the sea world. Fuel quality is already controlled by international standards drawn up by ISO. These standards should be improved to reduce air pollution due to sea transportation

Recent Global Warming As Depicted by AIRS, GISSTEMP, and MERRA-2

Science.gov (United States)

Susskind, J.; Iredell, L. F.; Lee, J. N.

2017-12-01

We observed anomalously warm global mean surface temperatures since 2015. The year 2016 represents the warmest annual mean surface skin and surface air temperatures in the AIRS observational period, September 2002 through August 2017. Additionally, AIRS monthly mean surface skin temperature, from January 2016 through September 2016, and November 2016, were the warmest observed for each month of the year. Continuing this trend, the AIRS global surface temperatures of 2017 February and April show the second greatest positive anomalies from average. This recent warming is particularly significant over the Arctic where the snow and sea ice melt is closely tied to the spring and summer surface temperatures. In this paper, we show the global distribution of surface temperature anomalies as observed by AIRS over the period September 2002 through August 2017 and compare them with those from the GISSTEMP and MERRA-2 surface temperatures. The spatial patterns of warm and cold anomalies for a given month show reasonably good agreement in all three data set. AIRS anomalies, which do not have the benefit of in-situ measurements, are in almost perfect agreement with those of MERRA-2, which does use in-situ surface measurements. GISSTEMP anomaly patterns for the most part look similar to those of AIRS and MERRA-2, but are more spread out spatially, and consequently are also weaker.

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

Energy Technology Data Exchange (ETDEWEB)

Omar, Abdirahman M.

2003-07-01

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

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

International Nuclear Information System (INIS)

Omar, Abdirahman M.

2003-01-01

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

Ikaite crystal distribution in winter sea ice and implications for CO2 system dynamics

DEFF Research Database (Denmark)

Rysgaard, Søren; Søgaard, D.H.; Cooper, M.

2013-01-01

The precipitation of ikaite (CaCO3 ⋅ 6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikai...

Cleaner shipping. Trade off between air pollution, costs and refinery CO2 emissions

International Nuclear Information System (INIS)

De Wilde, H.P.J.; Kroon, P.

2008-05-01

Still subject to final approval in October 2008, the International Maritime Organisation (IMO) agreed on a maximum sulphur content of 0.5% for shipping fuels in 2020. This target will induce major changes in the global refinery industry. We have estimated the impact on the Dutch refinery industry, which annually produces about 8 million tons of heavy fuel oil for sea shipping, with refinery residues as main component. It is technically possible to convert all residues, although this process will cause an additional energy use of about one million tons of crude oil and a related CO2 emission of about 4 million tons. The investment costs for these major changes in the Dutch refinery industry are estimated at about 1.5 tot 2 billion euros. The recent IMO agreement enables a gradual introduction of cleaner shipping fuels, which will reduce market disruptions and peak prices. Nevertheless, Rotterdam may not necessarily be able to develop a similar position in import, export and bunkering of future low sulphur fuels, compared to its present strong position in the market of heavy marine bunkers. Extrapolation of our national study to the global scale suggests that the deep conversion of 350 million tons of heavy fuel oil for shipping would require refinery investments in the order of 70-100 billion euros. The associated CO2 emissions would amount up to 175 Mton. The net additional CO2 emission, however, would be smaller since lighter shipping fuels result in less CO2 emissions at sea. On balance, we expect that the improvements in fuel economy, driven by the expensive low-carbon shipping fuels, will decrease CO2 emissions more than the increase in CO2 emissions from additional desulphurization in the refineries. Nevertheless CO2 emissions from sea shipping will continue to increase since marine transport is rapidly growing

Ikaite crystal distribution in Arctic winter sea ice and implications for CO2 system dynamics

DEFF Research Database (Denmark)

Rysgaard, Søren; Søgaard, D. H.; Cooper, M.

2012-01-01

The precipitation of ikaite (CaCO3·6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite...

Assessment of the sea-ice carbon pump

DEFF Research Database (Denmark)

Grimm, R.; Notz, D.; Glud, Ronnie N.

2016-01-01

-induced oceanic CO2 uptake ranges from 2 to 14 Tg C yr−1, which is up to 7% of the simulated net CO2 uptake in polar regions, but far less than 1% of the cur-rent global oceanic CO2 uptake. Hence, while we find that the SICP plays a minor role in the modern global carbon cycle, it is of importance......It has been suggested that geochemical processes related to sea-ice growth and melt might be important for the polar carbon cycle via the so called sea-ice carbon pump (SICP). The SICP affects the air-sea CO2 exchange by influencing the composition of dissolved inorganic carbon (DIC) and total...... for the regional carbon cycle at high latitudes....

Sea Ice as a Sink for CO2 and Biogeochemical Material: a Novel Sampling Method and Astrobiological Applications

Science.gov (United States)

Wilner, J.; Hofmann, A.; Hand, K. P.

2017-12-01

Accurately modelling the intensification of greenhouse gas effects in the polar regions ("polar amplification") necessitates a thorough understanding of the geochemical balance between atmospheric, sea ice, and oceanic layers. Sea ice is highly permeable to CO2 and therefore represents a major sink of oceanic CO2 in winter and of atmospheric CO2 in summer, sinks that are typically either poorly constrained in or fully absent from global climate models. We present a novel method for sampling both trapped and dissolved gases (CO2, CH4 and δ13CH4) in sea ice with a Picarro 2132-i Methane Analyzer, taking the following sampling considerations into account: minimization of water and air contamination, full headspace sampling, prevention of inadvertent sample bag double-puncturing, and ease of use. This method involves melting of vacuum-sealed ice cores to evacuate trapped gases to the headspace and sampling the headspace gas with a blunt needle sheathed by a beveled puncturing needle. A gravity catchment tube prevents input of dangerous levels of liquid water to the Picarro cavity. Subsequent ultrasonic degassing allows for dissolved gas measurement. We are in the process of using this method to sample gases trapped and dissolved in Arctic autumn sea ice cores and atmospheric samples collected during the 2016 Polarstern Expedition and during a May 2017 field campaign north of Barrow, Alaska. We additionally employ this method, together with inductively coupled plasma mass spectrometry (ICP-MS), to analyze the transfer of potential biogeochemical signatures of underlying hydrothermal plumes to sea ice. This has particular relevance to Europa and Enceladus, where hypothetical hydrothermal plumes may deliver seafloor chemicals to the overlying ice shell. Hence, we are presently investigating the entrainment of methane and other hydrothermal material in sea ice cores collected along the Gakkel Ridge that may serve as biosignatures of methanogenic organisms in seafloor

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

Tidal marsh plant responses to elevated CO2 , nitrogen fertilization, and sea level rise.

Science.gov (United States)

Adam Langley, J; Mozdzer, Thomas J; Shepard, Katherine A; Hagerty, Shannon B; Patrick Megonigal, J

2013-05-01

Elevated CO2 and nitrogen (N) addition directly affect plant productivity and the mechanisms that allow tidal marshes to maintain a constant elevation relative to sea level, but it remains unknown how these global change drivers modify marsh plant response to sea level rise. Here we manipulated factorial combinations of CO2 concentration (two levels), N availability (two levels) and relative sea level (six levels) using in situ mesocosms containing a tidal marsh community composed of a sedge, Schoenoplectus americanus, and a grass, Spartina patens. Our objective is to determine, if elevated CO2 and N alter the growth and persistence of these plants in coastal ecosystems facing rising sea levels. After two growing seasons, we found that N addition enhanced plant growth particularly at sea levels where plants were most stressed by flooding (114% stimulation in the + 10 cm treatment), and N effects were generally larger in combination with elevated CO2 (288% stimulation). N fertilization shifted the optimal productivity of S. patens to a higher sea level, but did not confer S. patens an enhanced ability to tolerate sea level rise. S. americanus responded strongly to N only in the higher sea level treatments that excluded S. patens. Interestingly, addition of N, which has been suggested to accelerate marsh loss, may afford some marsh plants, such as the widespread sedge, S. americanus, the enhanced ability to tolerate inundation. However, if chronic N pollution reduces the availability of propagules of S. americanus or other flood-tolerant species on the landscape scale, this shift in species dominance could render tidal marshes more susceptible to marsh collapse. © 2013 Blackwell Publishing Ltd.

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

Science.gov (United States)

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

2018-03-01

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

Remote sensing algorithm for sea surface CO2 in the Baltic Sea

Science.gov (United States)

Parard, G.; Charantonis, A. A.; Rutgerson, A.

2014-08-01

Studies of coastal seas in Europe have brought forth the high variability in the CO2 system. This high variability, generated by the complex mechanisms driving the CO2 fluxes makes their accurate estimation an arduous task. This is more pronounced in the Baltic Sea, where the mechanisms driving the fluxes have not been as highly detailed as in the open oceans. In adition, the joint availability of in-situ measurements of CO2 and of sea-surface satellite data is limited in the area. In this paper, a combination of two existing methods (Self-Organizing-Maps and Multiple Linear regression) is used to estimate ocean surface pCO2 in the Baltic Sea from remotely sensed surface temperature, chlorophyll, coloured dissolved organic matter, net primary production and mixed layer depth. The outputs of this research have an horizontal resolution of 4 km, and cover the period from 1998 to 2011. The reconstructed pCO2 values over the validation data set have a correlation of 0.93 with the in-situ measurements, and a root mean square error is of 38 μatm. The removal of any of the satellite parameters degraded this reconstruction of the CO2 flux, and we chose therefore to complete any missing data through statistical imputation. The CO2 maps produced by this method also provide a confidence level of the reconstruction at each grid point. The results obtained are encouraging given the sparsity of available data and we expect to be able to produce even more accurate reconstructions in the coming years, in view of the predicted acquisitions of new data.

A CO{sub 2} air conditioning system to fight against greenhouse effect; Une climatisation a CO{sub 2} pour lutter contre l'effet de serre

Energy Technology Data Exchange (ETDEWEB)

Anon.

2005-10-05

Automotive air-conditioning systems, with the induced additional fuel consumption and with the type of refrigerants used, contribute to the global warming. Several car fitters, like Delphi, have developed prototypes of CO{sub 2} air conditioners. CO{sub 2} is a greenhouse gas but is less harmful for the environment than other classical refrigerants. The use of CO{sub 2} needs a complete re-design of air-conditioning systems which have to stand pressures of 130 bars and temperatures of 165 deg. C. Short paper. (J.S.)

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.

CO2 Sink/Source in the Indonesian Seas

KAUST Repository

Kartadikaria, Aditya R.

2015-04-01

Two distinct CO2 sink/source characteristics appeared from the compiled observed data 1984-2013 in the tropical Indonesian seas. The western part persistently emits CO2 to the atmosphere, while the eastern is rather dynamic which emits and absorbs smaller amount of CO2 to and from atmosphere, respectively. The segregation is proximal to the virtual Wallace line, where in the continental shelf is located. Lower salinity and higher silicate condition in the western part influenced the higher pCO2 condition in Java Sea. Temperature is found to have a limited influence to control different characteristic in the west and east, but SST change of 2.0 0C during La Ninã condition effectively reduced the source amount of CO2 by 50% compared to Normal year condition. Yet, during La Ninã, higher wind speed increases CO2 flux twice compared to Normal year. In the continental shelf area where CO2 sink area is found, 29 years data showed that pCO2 trend is increasing ±0.6-3.8 μatm/year. From this study, the overall areas have a significant source of CO2 of approximately 10 - 24 μatm.

A multi-model assessment of the co-benefits of climate mitigation for global air quality

NARCIS (Netherlands)

Rao, Shilpa; Klimont, Zbigniew; Leitao, Joana; Riahi, Keywan; van Dingenen, Rita; Aleluia Reis, Lara; Calvin, Katherine; Dentener, Frank; Drouet, Laurent; Fujimori, Shinichiro; Harmsen, Mathijs; Luderer, Gunnar; Heyes, Chris; Strefler, Jessica; Tavoni, Massimo; van Vuuren, Detlef P.

2016-01-01

We present a model comparison study that combines multiple integrated assessment models with a reduced-form global air quality model to assess the potential co-benefits of global climate mitigation policies in relation to the World Health Organization (WHO) goals on air quality and health. We

CO{sub 2} emissions due to the air transportation in Brazil; Emissoes de CO{sub 2} devido ao transporte aereo no Brasil

Energy Technology Data Exchange (ETDEWEB)

Simoes, Andre Felipe; Schaeffer, Roberto [Universidade Federal, Rio de Janeiro, RJ (Brazil). Coordenacao dos Programas de Pos-graduacao de Engenharia. Programa de Planejamento Energetico]. E-mail: afsimoes@antares.com.br; roberto@ppe.ufrj.br

2002-07-01

This work intends to to insert and understand the participation of the brazilian air transportation in the ambit of the global climate changes. Firstly an introduction is presented for positioning the Brazil, in the proposed subject; an approach of the tenuous relationship between the air transportation sector and atmospheric environment medium; the energy consumption associated to the growing demand; and the inventory of the CO{sub 2} emissions (Calculated by using the top-down methodology) due to the Brazilian air transportation activities. The work is globally discussed and analysed.

Dynamic ikaite production and dissolution in sea ice – control by temperature, salinity and pCO₂ conditions

OpenAIRE

S. Rysgaard; F. Wang; R. J. Galley; R. Grimm; M. Lemes; N.-X. Geilfus; A. Chaulk; A. A. Hare; O. Crabeck; B. G. T. Else; K. Campbell; T. Papakyriakou; L. L. Sørensen; J. Sievers; D. Notz

2013-01-01

Ikaite is a hydrous calcium carbonate mineral (CaCO3 · 6H2O). It is only found in a metastable state, and decomposes rapidly once removed from near-freezing water. Recently, ikaite crystals have been found in sea ice and it has been suggested that their precipitation may play an important role in air-sea CO2 exchange in ice-covered seas. Little is known, however, of the spatial and temporal dynamics of ikaite in sea ice. Here we present evidence for highly dynamic ik...

Global ozone–CO correlations from OMI and AIRS: constraints on tropospheric ozone sources

Directory of Open Access Journals (Sweden)

P. S. Kim

2013-09-01

Full Text Available We present a global data set of free tropospheric ozone–CO correlations with 2° × 2.5° spatial resolution from the Ozone Monitoring Instrument (OMI and Atmospheric Infrared Sounder (AIRS satellite instruments for each season of 2008. OMI and AIRS have near-daily global coverage of ozone and CO respectively and observe coincident scenes with similar vertical sensitivities. The resulting ozone–CO correlations are highly statistically significant (positive or negative in most regions of the world, and are less noisy than previous satellite-based studies that used sparser data. Comparison with ozone–CO correlations and regression slopes (dO3/dCO from MOZAIC (Measurements of OZone, water vapour, carbon monoxide and nitrogen oxides by in-service AIrbus airCraft aircraft profiles shows good general agreement. We interpret the observed ozone–CO correlations with the GEOS (Goddard Earth Observing System-Chem chemical transport model to infer constraints on ozone sources. Driving GEOS-Chem with different meteorological fields generally shows consistent ozone–CO correlation patterns, except in some tropical regions where the correlations are strongly sensitive to model transport error associated with deep convection. GEOS-Chem reproduces the general structure of the observed ozone–CO correlations and regression slopes, although there are some large regional discrepancies. We examine the model sensitivity of dO3/dCO to different ozone sources (combustion, biosphere, stratosphere, and lightning NOx by correlating the ozone change from that source to CO from the standard simulation. The model reproduces the observed positive dO3/dCO in the extratropical Northern Hemisphere in spring–summer, driven by combustion sources. Stratospheric influence there is also associated with a positive dO3/dCO because of the interweaving of stratospheric downwelling with continental outflow. The well-known ozone maximum over the tropical South Atlantic is

Remote sensing the sea surface CO2 of the Baltic Sea using the SOMLO methodology

Science.gov (United States)

Parard, G.; Charantonis, A. A.; Rutgerson, A.

2015-06-01

Studies of coastal seas in Europe have noted the high variability of the CO2 system. This high variability, generated by the complex mechanisms driving the CO2 fluxes, complicates the accurate estimation of these mechanisms. This is particularly pronounced in the Baltic Sea, where the mechanisms driving the fluxes have not been characterized in as much detail as in the open oceans. In addition, the joint availability of in situ measurements of CO2 and of sea-surface satellite data is limited in the area. In this paper, we used the SOMLO (self-organizing multiple linear output; Sasse et al., 2013) methodology, which combines two existing methods (i.e. self-organizing maps and multiple linear regression) to estimate the ocean surface partial pressure of CO2 (pCO2) in the Baltic Sea from the remotely sensed sea surface temperature, chlorophyll, coloured dissolved organic matter, net primary production, and mixed-layer depth. The outputs of this research have a horizontal resolution of 4 km and cover the 1998-2011 period. These outputs give a monthly map of the Baltic Sea at a very fine spatial resolution. The reconstructed pCO2 values over the validation data set have a correlation of 0.93 with the in situ measurements and a root mean square error of 36 μatm. Removing any of the satellite parameters degraded this reconstructed CO2 flux, so we chose to supply any missing data using statistical imputation. The pCO2 maps produced using this method also provide a confidence level of the reconstruction at each grid point. The results obtained are encouraging given the sparsity of available data, and we expect to be able to produce even more accurate reconstructions in coming years, given the predicted acquisition of new data.

CO 2 Capture from Dilute Gases as a Component of Modern Global Carbon Management

KAUST Repository

Jones, Christopher W.

2011-01-01

The growing atmospheric CO2 concentration and its impact on climate have motivated widespread research and development aimed at slowing or stemming anthropogenic carbon emissions. Technologies for carbon capture and sequestration (CCS) employing mass separating agents that extract and purify CO2 from flue gas emanating from large point sources such as fossil fuel-fired electricity-generating power plants are under development. Recent advances in solvents, adsorbents, and membranes for postcombust- ion CO 2 capture are described here. Specifically, room-temperature ionic liquids, supported amine materials, mixed matrix and facilitated transport membranes, and metal-organic framework materials are highlighted. In addition, the concept of extracting CO2 directly from ambient air (air capture) as a means of reducing the global atmospheric CO2 concentration is reviewed. For both conventional CCS from large point sources and air capture, critical research needs are identified and discussed. © Copyright 2011 by Annual Reviews. All rights reserved.

CO 2 Capture from Dilute Gases as a Component of Modern Global Carbon Management

KAUST Repository

Jones, Christopher W.

2011-07-15

The growing atmospheric CO2 concentration and its impact on climate have motivated widespread research and development aimed at slowing or stemming anthropogenic carbon emissions. Technologies for carbon capture and sequestration (CCS) employing mass separating agents that extract and purify CO2 from flue gas emanating from large point sources such as fossil fuel-fired electricity-generating power plants are under development. Recent advances in solvents, adsorbents, and membranes for postcombust- ion CO 2 capture are described here. Specifically, room-temperature ionic liquids, supported amine materials, mixed matrix and facilitated transport membranes, and metal-organic framework materials are highlighted. In addition, the concept of extracting CO2 directly from ambient air (air capture) as a means of reducing the global atmospheric CO2 concentration is reviewed. For both conventional CCS from large point sources and air capture, critical research needs are identified and discussed. © Copyright 2011 by Annual Reviews. All rights reserved.

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

Dynamic ikaite production and dissolution in sea ice - control by temperature, salinity and pCO2 conditions

Science.gov (United States)

Rysgaard, S.; Wang, F.; Galley, R. J.; Grimm, R.; Lemes, M.; Geilfus, N.-X.; Chaulk, A.; Hare, A. A.; Crabeck, O.; Else, B. G. T.; Campbell, K.; Papakyriakou, T.; Sørensen, L. L.; Sievers, J.; Notz, D.

2013-12-01

Ikaite is a hydrous calcium carbonate mineral (CaCO3 · 6H2O). It is only found in a metastable state, and decomposes rapidly once removed from near-freezing water. Recently, ikaite crystals have been found in sea ice and it has been suggested that their precipitation may play an important role in air-sea CO2 exchange in ice-covered seas. Little is known, however, of the spatial and temporal dynamics of ikaite in sea ice. Here we present evidence for highly dynamic ikaite precipitation and dissolution in sea ice grown at an out-door pool of the Sea-ice Environmental Research Facility (SERF). During the experiment, ikaite precipitated in sea ice with temperatures below -3 °C, creating three distinct zones of ikaite concentrations: (1) a mm to cm thin surface layer containing frost flowers and brine skim with bulk concentrations of > 2000 μmol kg-1, (2) an internal layer with concentrations of 200-400 μmol kg-1 and (3) a~bottom layer with concentrations of ikaite crystals under acidic conditions. Manual removal of the snow cover allowed the sea ice to cool and brine salinities to increase, resulting in rapid ikaite precipitation. The modeled (FREZCHEM) ikaite concentrations were in the same order of magnitude as observations and suggest that ikaite concentration in sea ice increase with decreasing temperatures. Thus, varying snow conditions may play a key role in ikaite precipitation and dissolution in sea ice. This will have implications for CO2 exchange with the atmosphere and ocean.

Potential for reducing air-pollutants while achieving 2 °C global temperature change limit target.

Science.gov (United States)

Hanaoka, Tatsuya; Akashi, Osamu; Fujiwara, Kazuya; Motoki, Yuko; Hibino, Go

2014-12-01

This study analyzes the potential to reduce air pollutants while achieving the 2 °C global temperature change limit target above pre-industrial levels, by using the bottom-up optimization model, AIM/Enduse[Global]. This study focuses on; 1) estimating mitigation potentials and costs for achieving 2 °C, 2.5 °C, and 3 °C target scenarios, 2) assessing co-benefits of reducing air pollutants such as NOx, SO2, BC, PM, and 3) analyzing features of sectoral attributions in Annex I and Non-Annex I groups of countries. The carbon tax scenario at 50 US$/tCO2-eq in 2050 can reduce GHG emissions more than the 3 °C target scenario, but a higher carbon price around 400 US$/tCO2-eq in 2050 is required to achieve the 2 °C target scenario. However, there is also a co-benefit of large reduction potential of air pollutants, in the range of 60-80% reductions in 2050 from the reference scenario while achieving the 2 °C target. Copyright © 2014 Elsevier Ltd. All rights reserved.

High Precision Stable Isotope Measurements of Caribic Aircraft CO{sub 2} Samples: Global Distribution and Exchange with the Biosphere

Energy Technology Data Exchange (ETDEWEB)

Assonov, S. S. [Max Planck Institute for Chemistry, Mainz (Germany); Joint Research Centre, Institute for Reference Materials and Measurements (JRC-IRMM), European Commission, Geel (Belgium); Brenninkmeijer, C. A.M.; Schuck, T. J. [Max Planck Institute for Chemistry, Mainz (Germany); Taylor, P. [Joint Research Centre, Institute for Reference Materials and Measurements (JRC-IRMM), European Commission, Geel (Belgium)

2013-07-15

In 2007-2009 JRC-IRMM, in collaboration with the project CARIBIC (Civil Aircraft for Regular Investigation of the atmosphere Based on an Instrument Container, www.caribicatmospheric. com), conducted systematic measurements aimed to study the global distribution of CO{sub 2} isotopic composition. A large data set for the upper troposphere-lowermost stratosphere and free troposphere was obtained. For the first time it is demonstrated how CO{sub 2} isotope signals reflect global scale variability in air mass origin. Tight correlations observed arise either from stratosphere/troposphere mixing or from mixing of background air and air masses affected by CO{sub 2} sources and sinks, over long distances and throughout the seasons. The high quality {delta}{sup 18}O(CO{sub 2}) data prove to be a useful tracer reflecting long range CO{sub 2} transport and also CO{sub 2} exchange with land biosphere and soils. The data provide a benchmark for future comparisons and are available for modelling studies. (author)

Mechanisms controlling the air–sea CO2 flux in the North Sea

NARCIS (Netherlands)

Prowe, A.E.F.; Thomas, Helmuth; Pätsch, Johannes; Kühn, Wilfried; Bozec, Yann; Schiettecatte, Laure-Sophie; Borges, Alberto V.; Baar, Hein J.W. de; Paetsch, J; Kuehn, W

2009-01-01

The mechanisms driving the air–sea exchange of carbon dioxide (CO2) in the North Sea are investigated using the three-dimensional coupled physical–biogeochemical model ECOHAM (ECOlogical-model, HAMburg). We validate our simulations using field data for the years 2001–2002 and identify the controls

Climate warrior : David Keith and his team are engineering the world to manage global climate change : scrubbing CO{sub 2} out of the air we breathe

Energy Technology Data Exchange (ETDEWEB)

Eaton, S.

2009-01-15

A team of scientists from the University of Calgary's Institute for Sustainable Energy, Environment and Economy have developed an innovative way to capture atmospheric carbon. The process involves reducing carbon dioxide (CO{sub 2}) using a simple machine that can capture the trace amount of CO{sub 2} present in ambient air anywhere in the world. The research offers a way to capture CO{sub 2} emissions from transportation sources such as vehicles and airplanes, which represent about 50 per cent of global annual greenhouse gas emissions. This article described how the custom-built prototype air capture tower, called a contractor, works. It measures 6 metres tall by 1.2 metres wide and runs on a gasoline-powered generator. The energy efficient and cost effective air capture technology complements other approaches for reducing emissions from the transportation sector, such as biofuels and electric vehicles. The air capture tower can capture the CO{sub 2} that is present in ambient air and store it wherever it is cheapest. The custom-built tower can capture the equivalent of 20 tonnes per year of CO{sub 2} on a single square meter of scrubbing material. The team devised a way to use a chemical process from the pulp and paper industry to cut the energy cost of air capture in half. The simple, reliable and scalable technology offers an opportunity to build a commercial-scale plant. 1 ref., 6 figs.

CO2 Capture from the Air: Technology Assessment and Implications for Climate Policy

Science.gov (United States)

Keith, D. W.

2002-05-01

for global climate policy are examined using DIAM [2], a stylized integrated assessment model. We find that air capture can fundamentally alter the temporal dynamics of global warming mitigation. The reason for this is that air capture differs from conventional mitigation in three key aspects. First, it removes emissions from any part of the economy with equal ease or difficulty, so its cost provides an absolute cap on the cost of mitigation. Second, it permits reduction in concentrations faster than the natural carbon cycle: the effects of irreversibility are thus partly alleviated. Third, because it is less coupled with the energy system, air capture may offer stronger economies of scale and smaller adjustment costs than the more conventional mitigation technologies. Air capture limits the total cost of a worst-case climate scenario. In an optimal sequential decision framework with uncertainty, existence of air capture decreases the need for near-term precautionary abatement. Like geoengineering, air capture thus poses a moral hazard. 1. S. Elliott, et al. Compensation of atmospheric CO2 buildup through engineered chemical sinkage. Geophys. Res. Let., 28:1235-1238, 2001. 2. Minh Ha-Duong, Michael J. Grubb, and Jean-Charles Hourcade. Influence of socioeconomic inertia and uncertainty on optimal CO2-emission abatement. Nature, 390: 270-274, 1997.

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.

Ikaite crystals in melting sea ice – implications for pCO2 and pH levels in Arctic surface waters

DEFF Research Database (Denmark)

Rysgaard, Søren; Glud, R.N.; Lennert, K.

2012-01-01

A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air-sea CO 2 exchange. This has been complicated by the recent discoveries of ikaite (a polymorph of CaCO 3•6H 2O) in Arctic and Antarctic sea ice, which indicate that multiple...... chemical transformations occur in sea ice with a possible effect on CO 2 and pH conditions in surface waters. Here, we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from a melting 1.7 km 2 (0.5-1 m thick) drifting ice floe in the Fram Strait...... during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced...

Co-benefits of global, domestic, and sectoral greenhouse gas mitigation for US air quality and human health in 2050

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yuqiang; Smith, Steven J.; Bowden, Jared H.; Adelman, Zachariah; West, J. Jason

2017-11-01

Policies to reduce greenhouse gas (GHG) emissions can bring ancillary benefits of improved air quality and reduced premature mortality, in addition to slowing climate change. Here we study the co-benefits of global and domestic GHG mitigation on US air quality and human health in 2050 at fine resolution using dynamical downscaling, and quantify for the first time the co-benefits from foreign GHG mitigation. Relative to a reference scenario, global GHG reductions in RCP4.5 avoid 16000 PM2.5-related all-cause deaths yr-1 (90% confidence interval, 11700-20300), and 8000 (3600-12400) O3-related respiratory deaths yr-1 in the US in 2050. Foreign GHG mitigation avoids 15% and 62% of PM2.5- and O3-related total avoided deaths, highlighting the importance of foreign GHG mitigation on US human health benefits. GHG mitigation in the US residential sector brings the largest co-benefits for PM2.5-related deaths (21% of total domestic co-benefits), and industry for O3 (17%). Monetized benefits, for avoided deaths from ozone, PM2.5, and heat stress from a related study, are $148 ($96-201) per ton CO2 at high valuation and $49 ($32-67) at low valuation, of which 36% are from foreign GHG reductions. These benefits likely exceed the marginal cost of GHG reductions in 2050. The US gains significantly greater co-benefits when coordinating GHG reductions with foreign countries. Similarly, previous studies estimating co-benefits locally or regionally may greatly underestimate the full co-benefits of coordinated global actions.

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

Science.gov (United States)

Marinov, I.; Gnanadesikan, A.

2011-02-01

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

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

Directory of Open Access Journals (Sweden)

A. Gnanadesikan

2011-02-01

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

Trends in global CO2 emissions. 2012 Report

Energy Technology Data Exchange (ETDEWEB)

Olivier, J.G.J.; Peters, J.A.H.W. [PBL Netherlands Environmental Assessment Agency, Den Haag (Netherlands); Janssens-Maenhout, G. [Institute for Environment and Sustainability IES, European Commission' s Joint Research Centre JRC, Ispra (Italy)

2012-07-15

This report discusses the results of a trend assessment of global CO2 emissions up to 2011 and updates last year's assessment. This assessment focusses on the changes in annual CO2 emissions from 2010 to 2011, and includes not only fossil fuel combustion on which the BP reports are based, but also incorporates all other relevant CO2 emissions sources including flaring of waste gas during oil production, cement clinker production and other limestone uses, feedstock and other non-energy uses of fuels, and several other small sources. After a short description of the methods used (Chapter 2), we first present a summary of recent CO2 emission trends, by region and by country, and of the underlying trend of fossil fuel use, non-fossil energy and of other CO2 sources (Chapter 3). To provide a broader context of the global trends we also assess the cumulative global CO2 emissions of the last decade, i.e. since 2000, and compare it with scientific literature that analyse global emissions in relation to the target of 2C maximum global warming in the 21st century, which was adopted in the UN climate negotiations (Chapter 4). Compared to last year's report, Annex 1 includes a more detailed and updated discussion of the uncertainty in national and global CO2 emission estimates.

Trends in global CO2 emissions. 2012 Report

Energy Technology Data Exchange (ETDEWEB)

Olivier, J. G.J.; Peters, J. A.H.W. [PBL Netherlands Environmental Assessment Agency, Den Haag (Netherlands); Janssens-Maenhout, G. [Institute for Environment and Sustainability IES, European Commission' s Joint Research Centre JRC, Ispra (Italy)

2012-07-15

This report discusses the results of a trend assessment of global CO2 emissions up to 2011 and updates last year's assessment. This assessment focusses on the changes in annual CO2 emissions from 2010 to 2011, and includes not only fossil fuel combustion on which the BP reports are based, but also incorporates all other relevant CO2 emissions sources including flaring of waste gas during oil production, cement clinker production and other limestone uses, feedstock and other non-energy uses of fuels, and several other small sources. After a short description of the methods used (Chapter 2), we first present a summary of recent CO2 emission trends, by region and by country, and of the underlying trend of fossil fuel use, non-fossil energy and of other CO2 sources (Chapter 3). To provide a broader context of the global trends we also assess the cumulative global CO2 emissions of the last decade, i.e. since 2000, and compare it with scientific literature that analyse global emissions in relation to the target of 2C maximum global warming in the 21st century, which was adopted in the UN climate negotiations (Chapter 4). Compared to last year's report, Annex 1 includes a more detailed and updated discussion of the uncertainty in national and global CO2 emission estimates.

Effects of Northern Hemisphere Sea Surface Temperature Changes on the Global Air Quality

Science.gov (United States)

Yi, K.; Liu, J.

2017-12-01

The roles of regional sea surface temperature (SST) variability on modulating the climate system and consequently the air quality are investigated using the Community Earth System Model (CESM). Idealized, spatially uniform SST anomalies of +/- 1 °C are superimposed onto the North Pacific, North Atlantic, and North Indian Oceans individually. Ignoring the response of natural emissions, our simulations suggest large seasonal and regional variability of surface O3 and PM2.5 concentrations in response to SST anomalies, especially during boreal summers. Increasing the SST by 1 °C in one of the oceans generally decreases the surface O3 concentrations from 1 to 5 ppbv while increases the anthropogenic PM2.5 concentrations from 0.5 to 3 µg m-3. We implement the integrated process rate (IPR) analysis in CESM and find that meteorological transport in response to SST changes is the key process causing air pollutant perturbations in most cases. During boreal summers, the increase in tropical SST over different ocean basins enhances deep convection, which significantly increases the air temperature over the upper troposphere and trigger large-scale subsidence over nearby and remote regions. These processes tend to increase tropospheric stability and suppress rainfall at lower mid-latitudes. Consequently, it reduces the vertical transport of O3 to the surface while facilitating the accumulation of PM2.5 concentrations over most regions. In addition, this regional SST warming may also considerably suppress intercontinental transport of air pollution as confirmed with idealized CO-like tracers. Our findings indicate a robust linkage between basin-scale SST variability and regional air quality, which can help local air quality management.

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.

Ikaite crystal distribution in winter sea ice and implications for CO2 system dynamics

Science.gov (United States)

Rysgaard, S.; Søgaard, D. H.; Cooper, M.; Pućko, M.; Lennert, K.; Papakyriakou, T. N.; Wang, F.; Geilfus, N. X.; Glud, R. N.; Ehn, J.; McGinnis, D. F.; Attard, K.; Sievers, J.; Deming, J. W.; Barber, D.

2013-04-01

The precipitation of ikaite (CaCO3 ⋅ 6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few μm to 700 μm, were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surface-ice values of 700-900 μmol kg-1 ice (~25 × 106 crystals kg-1) to values of 100-200 μmol kg-1 ice (1-7 × 106 crystals kg-1) near the sea ice-water interface, all of which are much higher (4-10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration, whereas TA concentrations in the lower half of the sea ice were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolve in layers below. Melting of sea ice and dissolution of observed concentrations of ikaite would result in meltwater with a pCO2 of <15 μatm. This value is far below atmospheric values of 390 μatm and surface water concentrations of 315 μatm. Hence, the meltwater increases the potential for seawater uptake of CO2.

Coastal upwelling fluxes of O2, N2O, and CO2 assessed from continuous atmospheric observations at Trinidad, California

Directory of Open Access Journals (Sweden)

T. J. Lueker

2004-01-01

Full Text Available Continuous atmospheric records of O2/N2, CO2 and N2O obtained at Trinidad, California document the effects of air-sea exchange during coastal upwelling and plankton bloom events. The atmospheric records provide continuous observations of air-sea fluxes related to synoptic scale upwelling events over several upwelling seasons. Combined with satellite, buoy and local meteorology data, calculated anomalies in O2/N2 and N2O were utilized in a simple atmospheric transport model to compute air-sea fluxes during coastal upwelling. CO2 fluxes were linked to the oceanic component of the O2 fluxes through local hydrographic data and estimated as a function of upwelling intensity (surface ocean temperature and wind speed. Regional air-sea fluxes of O2/N2, N2O, and CO2 during coastal upwelling were estimated with the aid of satellite wind and SST data. Upwelling CO2 fluxes were found to represent ~10% of export production along the northwest coast of North America. Synoptic scale upwelling events impact the net exchange of atmospheric CO2 along the coastal margin, and will vary in response to the frequency and duration of alongshore winds that are subject to climate change.

Rolling stones. Fast weathering of olivine in shallow seas for cost-effective CO2 capture and mitigation of global warming and ocean acidification

Energy Technology Data Exchange (ETDEWEB)

Schuiling, R.D.; De Boer, P.L. [Department of Earth Sciences, Utrecht University, P.O. Box 80.021, 3508TA Utrecht (Netherlands)

2011-07-01

Human CO2 emissions may drive the Earth into a next greenhouse state. They can be mitigated by accelerating weathering of natural rock under the uptake of CO2. We disprove the paradigm that olivine weathering in nature would be a slow process, and show that it is not needed to mill olivine to very fine, 10 {mu}m-size grains in order to arrive at a complete dissolution within 1-2 year. In high-energy shallow marine environments olivine grains and reaction products on the grain surfaces, that otherwise would greatly retard the reaction, are abraded so that the chemical reaction is much accelerated. When kept in motion even large olivine grains rubbing and bumping against each other quickly produce fine clay- and silt-sized olivine particles that show a fast chemical reaction. Spreading of olivine in the world's 2% most energetic shelf seas can compensate a year's global CO2 emissions and counteract ocean acidification against a price well below that of carbon credits.

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

OpenAIRE

A. Gnanadesikan; I. Marinov

2010-01-01

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

Diurnal variability of CO2 flux at coastal zone of Taiwan based on eddy covariance observation

Science.gov (United States)

Chien, Hwa; Zhong, Yao-Zhao; Yang, Kang-Hung; Cheng, Hao-Yuan

2018-06-01

In this study, we employed shore-based eddy covariance systems for a continuous measurement of the coastal CO2 flux near the northwestern coast of Taiwan from 2011 to 2015. To ensure the validity of the analysis, the data was selected and filtered with a footprint model and an empirical mode decomposition method. The results indicate that the nearshore air-sea and air-land CO2 fluxes exhibited a significant diurnal variability and a substantial day-night difference. The net air-sea CO2 flux was -1.75 ± 0.98 μmol-C m-2 s-1, whereas the net air-land CO2 flux was 0.54 ± 7.35 μmol-C m-2 s-1, which indicated that in northwestern Taiwan, the coastal water acts as a sink of atmospheric CO2 but the coastal land acts as a source. The Random Forest Method was applied to hierarchize the influence of Chl-a, SST, DO, pH and U10 on air-sea CO2 fluxes. The result suggests that the strength of the diurnal air-sea CO2 flux is strongly influenced by the local wind speed.

Is there a decrease in the sink of atmospheric CO2 in the Nordic seas?

International Nuclear Information System (INIS)

Olsen, Are; Anderson, Leif G.

2002-01-01

It is well known that the seas off Norway sink a lot of carbon dioxide from the atmosphere, mainly because of the large heat loss from the sea in the area, which makes CO 2 more soluble in the water. Whether this sink has increased after the industrial revolution and thereby contributes to slowing down the increase of atmospheric CO 2 is uncertain. That is, it is uncertain whether there is a sink of anthropogenic CO 2 . There are indications that the opposite is true, that the sink of CO 2 in this area has slowed down along with the rise in the concentration of atmospheric CO 2 . Storing of anthropogenic CO 2 , however, takes place at higher latitudes where deep-water formation occurs, such as in the Nordic seas, where water that is saturated with anthropogenic CO 2 is transported down in the deep sea and becomes shielded from the atmosphere. Model calculations show that increased CO 2 in the atmosphere will reduce the sink of this gas in the Nordic seas. This conclusion is supported by observations from the Barents Sea

Will technological progress be sufficient to stabilize CO2 emissions from air transport in the mid-term?

International Nuclear Information System (INIS)

Cheze, Benoit; Chevallier, Julien; Gastineau, Pascal

2012-01-01

This article investigates whether anticipated technological progress can be expected to be strong enough to offset carbon dioxide (CO 2 ) emissions resulting from the rapid growth of air transport. Aviation CO 2 emissions projections are provided at the worldwide level and for eight geographical zones until 2025. Total air traffic flows are first forecast using a dynamic panel-data econometric model, and then converted into corresponding quantities of air traffic CO 2 emissions using specific hypotheses and energy factors. None of our nine scenarios appears compatible with the objective of 450 ppm CO 2 -eq. (a.k.a. 'scenario of type I') recommended by the Intergovernmental Panel on Climate Change (IPCC). None is either compatible with the IPCC scenario of type III, which aims at limiting global warming to 3.2 deg. C

Summer Distribution of Co2 Partial Pressure In The Ross Sea, Antarctica, and Relations With Biological Activity

Science.gov (United States)

Sandrini, S.; Tositti, L.; Tubertini, O.; Ceradini, S.; Palucci, A.; Barbini, R.; Fantoni, R.; Colao, F.; Ferrari, G. M.

The oceans play a key role in the processes responsible for global climate changes, in fact the oceanic uptake of anthropogenic atmospheric carbon dioxide is estimated to be 17-39The Southern Ocean and Antarctic marginal seas are considered to absorb up to half of this fraction. The Ross Sea, during the summer pack-ice melting, expe- riences rapid seasonal outgrowths, giving rise to phytoplankton blooms, especially in polynya areas near the coast line. This has a direct influence on pCO2 concentration in surface water, and hence on CO2 fluxes between ocean and atmosphere. Both the Ross Sea and the Southern Ocean transect between New Zealand and Antarctica are sys- tematically investigated during Italian Antarctic oceanographic campaigns onboard of the R/V Italica. During the XVI expedition, which took place in January and Febru- ary 2001, simultaneous measurements of surface pCO2 and Chlorophyll-a by laser remote-sensing apparatus were collected. Chlorophyll-a and pCO2 showed a general anticorrelation along the cruise. The survey has revealed the presence of high produc- tive regions in the polynya and close to the ice edge. The linear regression analysis of the chl-a vs pCO2 values improved our knowledge of the time evolution of the phyto- planktonic growth, independently measured by means of the laser yield, thus allowing for discrimination between different initial and final blooms in the Antarctic Ross Sea. The results obtained are here presented and discussed. They confirm the importance of biological production in the net absorption of atmospheric CO2 in continental shelf zones.

Assessing the effectiveness of global air-pollution treaties on CO2 emissions

OpenAIRE

Aurelie Slechten; Vincenzo Verardi

2014-01-01

This paper considers the effect of international air-pollution agreements ratified since 1970 on carbon dioxide emissions (CO2), the main cause of anthropogenic climate change. The analysis is based on a panel dataset of 150 countries over the period 1970-2008. While the literature generally focuses on one particular agreement, we analyze the effect of the accumulation of agreements using a two-way (country, year) fixed effects regression model. We find that the relationship between the numbe...

Global energy / CO2 projections

International Nuclear Information System (INIS)

Sinyak, Y.

1990-09-01

Section headings are: (1) Social and economic problems of the 21 st century and the role of energy supply systems (2) Energy-environment interactions as a central point of energy research activities (3) New ways of technological progress and its impacts on energy demand and supply (4) Long-term global energy projections (5) Comparative analysis of global long-term energy / CO 2 studies (6) Conclusions. The author shows that, in order to alleviate the negative impacts of energy systems on the climate, it will be necessary to undertake tremendous efforts to improve the energy use efficiency, to drastically change the primary energy mix, and, at the same time, to take action to reduce greenhouse emissions from other sources and increase the CO 2 sink through enhanced reforestation. (Quittner)

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

TG-FTIR measurement of CO2-H2O co-adsorption for CO2 air capture sorbent screening

NARCIS (Netherlands)

Smal, I.M.; Yu, Qian; Veneman, Rens; Fränzel-Luiten, B.; Brilman, Derk Willem Frederik

2014-01-01

Capturing atmospheric CO2 using solid sorbents is gaining interest. As ambient air normally contains much more (up to 100 times) water than CO2, a selective sorbent is desirable as co-adsorption will most likely occur. In this study, a convenient method based on an TG-FTIR analysis system is

Trends in global CO2 emissions. 2013 Report

Energy Technology Data Exchange (ETDEWEB)

Olivier, J.G.J.; Peters, J.A.H.W. [PBL Netherlands Environmental Assessment Agency, Den Haag (Netherlands); Janssens-Maenhout, G. [Institute for Environment and Sustainability IES, European Commission' s Joint Research Centre JRC, Ispra (Italy); Muntean, M. [Institute for Environment and Sustainability IES, Joint Research Centre JRC, Ispra (Italy)

2013-10-15

This report discusses the results of a trend assessment of global CO2 emissions up to 2012 and updates last year's assessment. This assessment focuses on the changes in annual CO2 emissions from 2011 to 2012, and includes not only fossil-fuel combustion on which the BP reports are based, but also incorporates other relevant CO2 emissions sources including flaring of waste gas during gas and oil production, cement clinker production and other limestone uses, feedstock and other non-energy uses of fuels, and several other small sources. The report clarifies the CO2 emission sources covered, and describes the methodology and data sources. More details are provided in Annex 1 over the 2010-2012 period, including a discussion of the degree of uncertainty in national and global CO2 emission estimates. Chapter 2 presents a summary of recent CO2 emission trends, per main country or region, including a comparison between emissions per capita and per unit of Gross Domestic Product (GDP), and of the underlying trend in fossil-fuel production and use, non-fossil energy and other CO2 sources. Specific attention is given to developments in shale gas and oil production and oil sands production and their impact on CO2 emissions. To provide a broader context of global emissions trends, international greenhouse gas mitigation targets and agreements are also presented, including different perspectives of emission accounting per country. In particular, annual trends with respect to the Kyoto Protocol target and Cancun agreements and cumulative global CO2 emissions of the last decade are compared with scientific literature that analyses global emissions in relation to the target of 2{sup 0}C maximum global warming in the 21st century, which was adopted in the UN climate negotiations. In addition, we briefly discuss the rapid development and implementation of various emission trading schemes, because of their increasing importance as a cross-cutting policy instrument for mitigating

Acidification at the Surface in the East Sea: A Coupled Climate-carbon Cycle Model Study

Science.gov (United States)

Park, Young-Gyu; Seol, Kyung-Hee; Boo, Kyung-On; Lee, Johan; Cho, Chunho; Byun, Young-Hwa; Seo, Seongbong

2018-05-01

This modeling study investigates the impacts of increasing atmospheric CO2 concentration on acidification in the East Sea. A historical simulation for the past three decades (1980 to 2010) was performed using the Hadley Centre Global Environmental Model (version 2), a coupled climate model with atmospheric, terrestrial and ocean cycles. As the atmospheric CO2 concentration increased, acidification progressed in the surface waters of the marginal sea. The acidification was similar in magnitude to observations and models of acidification in the global ocean. However, in the global ocean, the acidification appears to be due to increased in-situ oceanic CO2 uptake, whereas local processes had stronger effects in the East Sea. pH was lowered by surface warming and by the influx of water with higher dissolved inorganic carbon (DIC) from the northwestern Pacific. Due to the enhanced advection of DIC, the partial pressure of CO2 increased faster than in the overlying air; consequently, the in-situ oceanic uptake of CO2 decreased.

Measurements of CO2 Mole Fractionand δ13C in Archived Air Samples from Cape Meares, Oregon (USA) 1977 - 1998

Science.gov (United States)

Clark, O.; Rice, A. L.

2017-12-01

Carbon dioxide (CO2) is the most abundant, anthropogenically forced greenhouse gas (GHG) in the global atmosphere. Emissions of CO2 account for approximately 75% of the world's total GHG emissions. Atmospheric concentrations of CO2 are higher now than they've been at any other time in the past 800,000 years. Currently, the global mean concentration exceeds 400 ppm. Today, global networks regularly monitor CO2 concentrations and isotopic composition (δ13C and δ18O). However, past data is sparse. Over 200 ambient air samples from Cape Meares, Oregon (45.5°N, 124.0°W), a coastal site in Western United States, were obtained by researchers at Oregon Institute of Science and Technology (OGI, now Oregon Health & Science University), between the years of 1977 and 1998 as part of a global monitoring program of six different sites in the polar, middle, and tropical latitudes of the Northern and Southern Hemispheres. Air liquefaction was used to compress approximately 1000L of air (STP) to 30bar, into 33L electropolished (SUMMA) stainless steel canisters. Select archived air samples from the original network are maintained at Portland State University (PSU) Department of Physics. These archived samples are a valuable look at changing atmospheric concentrations of CO2 and δ13C, which can contribute to a better understanding of changes in sources during this time. CO2 concentrations and δ13C of CO2 were measured at PSU, with a Picarro Cavity Ringdown Spectrometer, model G1101-i analytical system. This study presents the analytical methods used, calibration techniques, precision, and reproducibility. Measurements of select samples from the archive show rising CO2 concentrations and falling δ13C over the 1977 to 1998 period, compatible with previous observations and rising anthropogenic sources of CO2. The resulting data set was statistically analyzed in MATLAB. Results of preliminary seasonal and secular trends from the archive samples are presented.

Monthly dynamics of carbon dioxide exchange across the sea surface of the Arctic Ocean in response to changes in gas transfer velocity and partial pressure of CO2 in 2010

Directory of Open Access Journals (Sweden)

Iwona Wrobel

2017-10-01

Full Text Available The Arctic Ocean (AO is an important basin for global oceanic carbon dioxide (CO2 uptake, but the mechanisms controlling air–sea gas fluxes are not fully understood, especially over short and long timescales. The oceanic sink of CO2 is an important part of the global carbon budget. Previous studies have shown that in the AO differences in the partial pressure of CO2 (ΔpCO2 and gas transfer velocity (k both contribute significantly to interannual air–sea CO2 flux variability, but that k is unimportant for multidecadal variability. This study combined Earth Observation (EO data collected in 2010 with the in situ pCO2 dataset from Takahashi et al. (2009 (T09 using a recently developed software toolbox called FluxEngine to determine the importance of k and ΔpCO2 on CO2 budgets in two regions of the AO – the Greenland Sea (GS and the Barents Sea (BS with their continental margins. Results from the study indicate that the variability in wind speed and, hence, the gas transfer velocity, generally play a major role in determining the temporal variability of CO2 uptake, while variability in monthly ΔpCO2 plays a major role spatially, with some exceptions.

Air-Sea Interactions in the Marginal Ice Zone

Science.gov (United States)

2016-03-31

elementascience.org Air-sea interactions in the marginal ice zoneAir-Sea interactions in the Marginal Ice Zone Seth Zippel1* • Jim Thomson1 1Applied...Bidlot, 2013; Collins -III et al., 2015). Spectral wave directions and spread are given in Figure 5, where the difference in wave and wind direction...359219a0. Chalikov DV, Belevich MY. 1993. One-dimensional theory of the wave boundary layer. Bound-Lay Meteor 63: 65–96. Collins -III CO, Rogers WE

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

Carbon Dioxide Transfer Through Sea Ice: Modelling Flux in Brine Channels

Science.gov (United States)

Edwards, L.; Mitchelson-Jacob, G.; Hardman-Mountford, N.

2010-12-01

For many years sea ice was thought to act as a barrier to the flux of CO2 between the ocean and atmosphere. However, laboratory-based and in-situ observations suggest that while sea ice may in some circumstances reduce or prevent transfer (e.g. in regions of thick, superimposed multi-year ice), it may also be highly permeable (e.g. thin, first year ice) with some studies observing significant fluxes of CO2. Sea ice covered regions have been observed to act both as a sink and a source of atmospheric CO2 with the permeability of sea ice and direction of flux related to sea ice temperature and the presence of brine channels in the ice, as well as seasonal processes such as whether the ice is freezing or thawing. Brine channels concentrate dissolved inorganic carbon (DIC) as well as salinity and as these dense waters descend through both the sea ice and the surface ocean waters, they create a sink for CO2. Calcium carbonate (ikaite) precipitation in the sea ice is thought to enhance this process. Micro-organisms present within the sea ice will also contribute to the CO2 flux dynamics. Recent evidence of decreasing sea ice extent and the associated change from a multi-year ice to first-year ice dominated system suggest the potential for increased CO2 flux through regions of thinner, more porous sea ice. A full understanding of the processes and feedbacks controlling the flux in these regions is needed to determine their possible contribution to global CO2 levels in a future warming climate scenario. Despite the significance of these regions, the air-sea CO2 flux in sea ice covered regions is not currently included in global climate models. Incorporating this carbon flux system into Earth System models requires the development of a well-parameterised sea ice-air flux model. In our work we use the Los Alamos sea ice model, CICE, with a modification to incorporate the movement of CO2 through brine channels including the addition of DIC processes and ice algae production to

Accumulation of fossil CO/sub 2/ in the atmosphere and the sea

Energy Technology Data Exchange (ETDEWEB)

Fairhall, A W

1973-09-07

A model is presented which accounts quantitatively for the buildup of fossil CO/sub 2/ in the atmosphere. The model also predicts something not previously recognized: a significant uptake of fossil CO/sub 2/ by the sea. The sea is presently supersaturated with respect to aragonite and calcite, which calcareous organisms form in building their shells. Should the sea become unsaturated in CaCO/sub 3/ the shells of these organisms would tend to dissolve, as would the ocean's coral reefs. One test of the model would be afforded by careful monitoring of total CO/sub 2/ levels in the mixed layer over the next few years. The model predicts an increase in the mixed layer of about 1.4 per cent in the next decade. Because this is about double the accuracy of the present methods for measuring total CO/sub 2/ in seawater, this trend, if present, should be detectable within 3 to 5 years. (MFB)

Air quality co-benefits of carbon pricing in China

Science.gov (United States)

Li, Mingwei; Zhang, Da; Li, Chiao-Ting; Mulvaney, Kathleen M.; Selin, Noelle E.; Karplus, Valerie J.

2018-05-01

Climate policies targeting energy-related CO2 emissions, which act on a global scale over long time horizons, can result in localized, near-term reductions in both air pollution and adverse human health impacts. Focusing on China, the largest energy-using and CO2-emitting nation, we develop a cross-scale modelling approach to quantify these air quality co-benefits, and compare them to the economic costs of climate policy. We simulate the effects of an illustrative climate policy, a price on CO2 emissions. In a policy scenario consistent with China's recent pledge to reach a peak in CO2 emissions by 2030, we project that national health co-benefits from improved air quality would partially or fully offset policy costs depending on chosen health valuation. Net health co-benefits are found to rise with increasing policy stringency.

Air toxic emissions from burning of biomass globally-preliminary results

International Nuclear Information System (INIS)

Ward, D.E.; Hao, W.M.

1992-01-01

Emissions of trace gases, particles, and air toxic substances in the smoke plumes from biomass fires are of importance to global climate change. The potential impact of the air toxic emissions on the human population of specific regions globally is another major concern. The toxic materials are produced in high concentrations in areas of heavy biomass burning, e.g., Amazon Basin and Central/southern Africa. We provide new estimates of air toxics based on the combustion efficiency (percent of total carbon released as CO 2 ) for fires burning in different ecosystems on a global basis. Estimates of total biomass consumed on a global basis range from 2 to 10 Pg (1 petagram = 10 15 g) per year. We apply emission factors for various air toxics (g of emission released per kg of fuel consumed) to the estimate of global biomass consumption of 6.4 Pg per year. The principal air toxics analyzed in this paper include: Total particulate matter, CO, formaldehyde, acetaldehyde, acrolein, benzene, toluene, o-xylene, m, p-xylene, benzo[a]pyrene, and polycyclic organic material. The total emissions calculated for these materials on a yearly global basis are: 75, 362, 4.9, 1.5, 1.5, 2.1, 2.1, 0.3, 0.6, 0.001, 0.026, Tg (1 teragram = 10 12 g) per year, respectively. Biomass burning in the United States contributes less than 3% to the total global emissions

CO2 Sink/Source in the Indonesian Seas

KAUST Repository

Kartadikaria, Aditya R.; Watanabe, Atsushi; Nadaoka, Kazuo; Prayitno, Hanif; Adi, Novi; Suharsono, Suharsono; Muchtar, Muswerry; Triyulianti, Iis; Setiawan, Agus; Suratno, Suratno; Khasanah, Elly

2015-01-01

condition in Java Sea. Temperature is found to have a limited influence to control different characteristic in the west and east, but SST change of 2.0 0C during La Ninã condition effectively reduced the source amount of CO2 by 50% compared to Normal year

TropFlux: air-sea fluxes for the global tropical oceans-description and evaluation

Digital Repository Service at National Institute of Oceanography (India)

PraveenKumar, B.; Vialard, J.; Lengaigne, M.; Murty, V.S.N.; McPhaden, M.J.

This paper evaluates several timely, daily air-sea heat flux products (NCEP, NCEP2, ERA-Interim and OAFlux/ISCCP) against observations and present the newly developed TropFlux product. This new product uses bias-corrected ERA-interim and ISCCP data...

Pursuing air pollutant co-benefits of CO2 mitigation in China: A provincial leveled analysis

International Nuclear Information System (INIS)

Dong, Huijuan; Dai, Hancheng; Dong, Liang; Fujita, Tsuyoshi; Geng, Yong; Klimont, Zbigniew; Inoue, Tsuyoshi; Bunya, Shintaro; Fujii, Minoru; Masui, Toshihiko

2015-01-01

Highlights: • China’s future CO 2 reduction and its co-benefits on air pollutants were projected. • GAINS-China and AIM/CGE models were combined for emission and cost estimation. • High GDP regions tended to have higher emission, reduction potential and co-benefit. • Coal ratio and coal quality were also key factors to affect reduction and co-benefit. • Mitigation investment to less developed western regions was more effective. - Abstract: With fast economic development, industrialization and urbanization, China faces increasing pressures on carbon emission reduction, and especially on air pollutants (SO 2 , NOx, PM) reduction, particularly the notorious haze issue caused by air pollution in recent years. Pursuing co-benefits is an effective approach to simultaneously respond to both carbon and air pollutant problems. In this paper, the AIM/CGE (Asia–Pacific Integrated Assessment Model/Computational General Equilibrium) model and GAINS (Greenhouse Gas and Air Pollution Interactions and Synergies)-China model are combined together to project future CO 2 and air pollutants emissions in China, as well as reduction costs and co-benefit effects. Considering implementation of carbon mitigation policy and air pollutant mitigation technologies, four scenarios (S1, S2, S3 and S4) are analyzed. Results indicate that by implementing both carbon and air pollutant mitigation (S4), CO 2 emission per GDP can be reduced by 41% by 2020, compared with the 2005 level, and SO 2 , NOx and PM2.5 emissions would change by a factor 0.8, 1.26 and 1.0 of the 2005 level, respectively in 2030. The real co-benefits of emission reductions (S2 minus S4) for SO 2 , NOx and PM2.5 are 2.4 Mt, 2.1 Mt and 0.3 Mt in 2020, and the corresponding cost reduction co-benefits are 4, 0.11, and 0.8 billion €, respectively. Provincial disparity analysis reveals that regions with higher co-benefits are those with higher GDP such as Guangdong, Shandong and Jiangsu, energy production bases such as

Seasonal variation of CO{sub 2} flux between air and temperate forest

Energy Technology Data Exchange (ETDEWEB)

Yamamoto, Susumo; Murayama, Shohei; Kondo, Hiroaki [National Inst. for Resources and Environment, Ibaraki (Japan)

1995-12-31

Carbon dioxide, which is a very important greenhouse gas, contributes approximately 55 % to the problem of global warming. The knowledge to the sources and sinks of carbon on a global basis is very poor. IPCC (1994) suggested that unknown 1.5-2.0 GtC/year may be sunk in terrestrial ecosystem, in particular, in the Northern Hemisphere. As can be seen from a recent estimation of the carbon fluxes in the terrestrial biosphere, there is a high degree of uncertainty in the magnitude. The clear evidence for it has not been shown yet by IPCC (1994). However, based on the gradient of CO{sub 2}, as a function of latitude, main CO{sub 2} sink can be thought to be in the terrestrial biosphere, in the middle to high latitude of the Northern Hemisphere. As can be seen from a recent estimation of the carbon fluxes in the terrestrial biosphere, there is a high degree of uncertainty in the magnitude. From this view, more investigation of the role of the temperate forest on the CO{sub 2} balance is inevitable. In this presentation, the seasonal variation of CO{sub 2} flux between air and biosphere in temperate deciduous forest in Japan is intended to be elucidated. (author)

Seasonal variation of CO{sub 2} flux between air and temperate forest

Energy Technology Data Exchange (ETDEWEB)

Yamamoto, Susumo; Murayama, Shohei; Kondo, Hiroaki [National Inst. for Resources and Environment, Ibaraki (Japan)

1996-12-31

Carbon dioxide, which is a very important greenhouse gas, contributes approximately 55 % to the problem of global warming. The knowledge to the sources and sinks of carbon on a global basis is very poor. IPCC (1994) suggested that unknown 1.5-2.0 GtC/year may be sunk in terrestrial ecosystem, in particular, in the Northern Hemisphere. As can be seen from a recent estimation of the carbon fluxes in the terrestrial biosphere, there is a high degree of uncertainty in the magnitude. The clear evidence for it has not been shown yet by IPCC (1994). However, based on the gradient of CO{sub 2}, as a function of latitude, main CO{sub 2} sink can be thought to be in the terrestrial biosphere, in the middle to high latitude of the Northern Hemisphere. As can be seen from a recent estimation of the carbon fluxes in the terrestrial biosphere, there is a high degree of uncertainty in the magnitude. From this view, more investigation of the role of the temperate forest on the CO{sub 2} balance is inevitable. In this presentation, the seasonal variation of CO{sub 2} flux between air and biosphere in temperate deciduous forest in Japan is intended to be elucidated. (author)

Impacts of South East Biomass Burning on local air quality in South China Sea

Science.gov (United States)

Wai-man Yeung, Irene; Fat Lam, Yun; Eniolu Morakinyo, Tobi

2016-04-01

Biomass burning is a significant source of carbon monoxide and particulate matter, which is not only contribute to the local air pollution, but also regional air pollution. This study investigated the impacts of biomass burning emissions from Southeast Asia (SEA) as well as its contribution to the local air pollution in East and South China Sea, including Hong Kong and Taiwan. Three years (2012 - 2014) of the Hybrid Single Particle Lagrangian-Integrated Trajectory (HYSPLIT) with particles dispersion analyses using NCEP (Final) Operational Global Analysis data (FNL) data (2012 - 2014) were analyzed to track down all possible long-range transport from SEA with a sinking motion that worsened the surface air quality (tropospheric downwash from the free troposphere). The major sources of SEA biomass burning emissions were first identified using high fire emissions from the Global Fire Emission Database (GFED), followed by the HYSPLIT backward trajectory dispersion modeling analysis. The analyses were compared with the local observation data from Tai Mo Shan (1,000 msl) and Tap Mun (60 msl) in Hong Kong, as well as the data from Lulin mountain (2,600 msl) in Taiwan, to assess the possible impacts of SEA biomass burning on local air quality. The correlation between long-range transport events from the particles dispersion results and locally observed air quality data indicated that the background concentrations of ozone, PM2.5 and PM10 at the surface stations were enhanced by 12 μg/m3, 4 μg/m3 and 7 μg/m3, respectively, while the long-range transport contributed to enhancements of 4 μg/m3, 4 μg/m3 and 8 μg/m3 for O3, PM2.5 and PM10, respectively at the lower free atmosphere.

Variability of 14C reservoir age and air-sea flux of CO2 in the Peru-Chile upwelling region during the past 12,000 years

Science.gov (United States)

Carré, Matthieu; Jackson, Donald; Maldonado, Antonio; Chase, Brian M.; Sachs, Julian P.

2016-01-01

The variability of radiocarbon marine reservoir age through time and space limits the accuracy of chronologies in marine paleo-environmental archives. We report here new radiocarbon reservoir ages (ΔR) from the central coast of Chile ( 32°S) for the Holocene period and compare these values to existing reservoir age reconstructions from southern Peru and northern Chile. Late Holocene ΔR values show little variability from central Chile to Peru. Prior to 6000 cal yr BP, however, ΔR values were markedly increased in southern Peru and northern Chile, while similar or slightly lower-than-modern ΔR values were observed in central Chile. This extended dataset suggests that the early Holocene was characterized by a substantial increase in the latitudinal gradient of marine reservoir age between central and northern Chile. This change in the marine reservoir ages indicates that the early Holocene air-sea flux of CO2 could have been up to five times more intense than in the late Holocene in the Peruvian upwelling, while slightly reduced in central Chile. Our results show that oceanic circulation changes in the Humboldt system during the Holocene have substantially modified the air-sea carbon flux in this region.

Global estimates of CO sources with high resolution by adjoint inversion of multiple satellite datasets (MOPITT, AIRS, SCIAMACHY, TES

Directory of Open Access Journals (Sweden)

M. Kopacz

2010-02-01

Full Text Available We combine CO column measurements from the MOPITT, AIRS, SCIAMACHY, and TES satellite instruments in a full-year (May 2004–April 2005 global inversion of CO sources at 4°×5° spatial resolution and monthly temporal resolution. The inversion uses the GEOS-Chem chemical transport model (CTM and its adjoint applied to MOPITT, AIRS, and SCIAMACHY. Observations from TES, surface sites (NOAA/GMD, and aircraft (MOZAIC are used for evaluation of the a posteriori solution. Using GEOS-Chem as a common intercomparison platform shows global consistency between the different satellite datasets and with the in situ data. Differences can be largely explained by different averaging kernels and a priori information. The global CO emission from combustion as constrained in the inversion is 1350 Tg a⁻¹. This is much higher than current bottom-up emission inventories. A large fraction of the correction results from a seasonal underestimate of CO sources at northern mid-latitudes in winter and suggests a larger-than-expected CO source from vehicle cold starts and residential heating. Implementing this seasonal variation of emissions solves the long-standing problem of models underestimating CO in the northern extratropics in winter-spring. A posteriori emissions also indicate a general underestimation of biomass burning in the GFED2 inventory. However, the tropical biomass burning constraints are not quantitatively consistent across the different datasets.

Global CO2 emissions from cement production

Science.gov (United States)

Andrew, Robbie M.

2018-01-01

The global production of cement has grown very rapidly in recent years, and after fossil fuels and land-use change, it is the third-largest source of anthropogenic emissions of carbon dioxide. The required data for estimating emissions from global cement production are poor, and it has been recognised that some global estimates are significantly inflated. Here we assemble a large variety of available datasets and prioritise official data and emission factors, including estimates submitted to the UNFCCC plus new estimates for China and India, to present a new analysis of global process emissions from cement production. We show that global process emissions in 2016 were 1.45±0.20 Gt CO2, equivalent to about 4 % of emissions from fossil fuels. Cumulative emissions from 1928 to 2016 were 39.3±2.4 Gt CO2, 66 % of which have occurred since 1990. Emissions in 2015 were 30 % lower than those recently reported by the Global Carbon Project. The data associated with this article can be found at https://doi.org/10.5281/zenodo.831455.

Forecasting global atmospheric CO2

International Nuclear Information System (INIS)

Agusti-Panareda, A.; Massart, S.; Boussetta, S.; Balsamo, G.; Beljaars, A.; Engelen, R.; Jones, L.; Peuch, V.H.; Chevallier, F.; Ciais, P.; Paris, J.D.; Sherlock, V.

2014-01-01

A new global atmospheric carbon dioxide (CO 2 ) real-time forecast is now available as part of the preoperational Monitoring of Atmospheric Composition and Climate - Interim Implementation (MACC-II) service using the infrastructure of the European Centre for Medium-Range Weather Forecasts (ECMWF) Integrated Forecasting System (IFS). One of the strengths of the CO 2 forecasting system is that the land surface, including vegetation CO 2 fluxes, is modelled online within the IFS. Other CO 2 fluxes are prescribed from inventories and from off-line statistical and physical models. The CO 2 forecast also benefits from the transport modelling from a state-of-the-art numerical weather prediction (NWP) system initialized daily with a wealth of meteorological observations. This paper describes the capability of the forecast in modelling the variability of CO 2 on different temporal and spatial scales compared to observations. The modulation of the amplitude of the CO 2 diurnal cycle by near-surface winds and boundary layer height is generally well represented in the forecast. The CO 2 forecast also has high skill in simulating day-to-day synoptic variability. In the atmospheric boundary layer, this skill is significantly enhanced by modelling the day-to-day variability of the CO 2 fluxes from vegetation compared to using equivalent monthly mean fluxes with a diurnal cycle. However, biases in the modelled CO 2 fluxes also lead to accumulating errors in the CO 2 forecast. These biases vary with season with an underestimation of the amplitude of the seasonal cycle both for the CO 2 fluxes compared to total optimized fluxes and the atmospheric CO 2 compared to observations. The largest biases in the atmospheric CO 2 forecast are found in spring, corresponding to the onset of the growing season in the Northern Hemisphere. In the future, the forecast will be re-initialized regularly with atmospheric CO 2 analyses based on the assimilation of CO 2 products retrieved from satellite

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.

CO2 Sink/Source Characteristics in the Tropical Indonesian Seas

KAUST Repository

Kartadikaria, Aditya R.; Watanabe, A.; Nadaoka, K.; Adi, N. S.; Prayitno, H. B.; Suharsono, S.; Muchtar, M.; Triyulianti, I.; Setiawan, A.; Suratno, S.; Khasanah, E. N.

2015-01-01

Two distinct CO2 sink/source characteristics are found in the tropical Indonesian seas from the compilation of observed data for the period 1984-2013. The western region persistently emits CO2 to the atmosphere, whereas the eastern region is dynamic and acts either as a small source or sink of CO2 to the atmosphere, depending on sites. The segregation is proximal to the Makassar Strait, which is located over the continental shelf and is one of the main routes of the Indonesian Throughflow (ITF). Lower salinity and higher silicate were found in the western region, suggesting a terrestrial influence in this area. Temperature has a limited influence in controlling different CO2 sink/source characteristics in the west and east. However, an SST change of -2.0°C during La Niña events effectively reduces the pCO2 difference between the atmosphere and surface seawater by 50% compared to normal year conditions. During La Niña events, higher wind speeds double the CO2 flux from the ocean to the atmosphere compared to that of a normal year. In the continental shelf area where the CO2 sink area was found, data of over 29 years show that the seawater pCO2 increased by 0.6-3.8 μatm yr−1. Overall, the seawater pCO2 of the Indonesian Seas is supersaturated relative to the atmosphere by 15.9 ± 8.6 μatm and thus acts as a source of CO2 to the atmosphere. This article is protected by copyright. All rights reserved.

CO2 Sink/Source Characteristics in the Tropical Indonesian Seas

KAUST Repository

Kartadikaria, Aditya R.

2015-11-05

Two distinct CO2 sink/source characteristics are found in the tropical Indonesian seas from the compilation of observed data for the period 1984-2013. The western region persistently emits CO2 to the atmosphere, whereas the eastern region is dynamic and acts either as a small source or sink of CO2 to the atmosphere, depending on sites. The segregation is proximal to the Makassar Strait, which is located over the continental shelf and is one of the main routes of the Indonesian Throughflow (ITF). Lower salinity and higher silicate were found in the western region, suggesting a terrestrial influence in this area. Temperature has a limited influence in controlling different CO2 sink/source characteristics in the west and east. However, an SST change of -2.0°C during La Niña events effectively reduces the pCO2 difference between the atmosphere and surface seawater by 50% compared to normal year conditions. During La Niña events, higher wind speeds double the CO2 flux from the ocean to the atmosphere compared to that of a normal year. In the continental shelf area where the CO2 sink area was found, data of over 29 years show that the seawater pCO2 increased by 0.6-3.8 μatm yr−1. Overall, the seawater pCO2 of the Indonesian Seas is supersaturated relative to the atmosphere by 15.9 ± 8.6 μatm and thus acts as a source of CO2 to the atmosphere. This article is protected by copyright. All rights reserved.

An analysis of the global spatial variability of column-averaged CO2 from SCIAMACHY and its implications for CO2 sources and sinks

Science.gov (United States)

Zhang, Zhen; Jiang, Hong; Liu, Jinxun; Zhang, Xiuying; Huang, Chunlin; Lu, Xuehe; Jin, Jiaxin; Zhou, Guomo

2014-01-01

Satellite observations of carbon dioxide (CO2) are important because of their potential for improving the scientific understanding of global carbon cycle processes and budgets. We present an analysis of the column-averaged dry air mole fractions of CO2 (denoted XCO2) of the Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) retrievals, which were derived from a satellite instrument with relatively long-term records (2003–2009) and with measurements sensitive to the near surface. The spatial-temporal distributions of remotely sensed XCO2 have significant spatial heterogeneity with about 6–8% variations (367–397 ppm) during 2003–2009, challenging the traditional view that the spatial heterogeneity of atmospheric CO2 is not significant enough (2 and surface CO2 were found for major ecosystems, with the exception of tropical forest. In addition, when compared with a simulated terrestrial carbon uptake from the Integrated Biosphere Simulator (IBIS) and the Emissions Database for Global Atmospheric Research (EDGAR) carbon emission inventory, the latitudinal gradient of XCO2 seasonal amplitude was influenced by the combined effect of terrestrial carbon uptake, carbon emission, and atmospheric transport, suggesting no direct implications for terrestrial carbon sinks. From the investigation of the growth rate of XCO2 we found that the increase of CO2 concentration was dominated by temperature in the northern hemisphere (20–90°N) and by precipitation in the southern hemisphere (20–90°S), with the major contribution to global average occurring in the northern hemisphere. These findings indicated that the satellite measurements of atmospheric CO2 improve not only the estimations of atmospheric inversion, but also the understanding of the terrestrial ecosystem carbon dynamics and its feedback to atmospheric CO2.

Air-sea exchange of gaseous mercury in the East China Sea.

Science.gov (United States)

Wang, Chunjie; Ci, Zhijia; Wang, Zhangwei; Zhang, Xiaoshan

2016-05-01

Two oceanographic cruises were carried out in the East China Sea (ECS) during the summer and fall of 2013. The main objectives of this study are to identify the spatial-temporal distributions of gaseous elemental mercury (GEM) in air and dissolved gaseous mercury (DGM) in surface seawater, and then to estimate the Hg(0) flux. The GEM concentration was lower in summer (1.61 ± 0.32 ng m(-3)) than in fall (2.20 ± 0.58 ng m(-3)). The back-trajectory analysis revealed that the air masses with high GEM levels during fall largely originated from the land, while the air masses with low GEM levels during summer primarily originated from ocean. The spatial distribution patterns of total Hg (THg), fluorescence, and turbidity were consistent with the pattern of DGM with high levels in the nearshore area and low levels in the open sea. Additionally, the levels of percentage of DGM to THg (%DGM) were higher in the open sea than in the nearshore area, which was consistent with the previous studies. The THg concentration in fall was higher (1.47 ± 0.51 ng l(-1)) than those of other open oceans. The DGM concentration (60.1 ± 17.6 pg l(-1)) and Hg(0) flux (4.6 ± 3.6 ng m(-2) h(-1)) in summer were higher than those in fall (DGM: 49.6 ± 12.5 pg l(-1) and Hg(0) flux: 3.6 ± 2.8 ng m(-2) h(-1)). The emission flux of Hg(0) from the ECS was estimated to be 27.6 tons yr(-1), accounting for ∼0.98% of the global Hg oceanic evasion though the ECS only accounts for ∼0.21% of global ocean area, indicating that the ECS plays an important role in the oceanic Hg cycle. Copyright © 2016 Elsevier Ltd. All rights reserved.

Impact of short-lived non-CO2 mitigation on carbon budgets for stabilizing global warming

International Nuclear Information System (INIS)

Rogelj, Joeri; Riahi, Keywan; Meinshausen, Malte; Schaeffer, Michiel; Knutti, Reto

2015-01-01

Limiting global warming to any level requires limiting the total amount of CO 2 emissions, or staying within a CO 2 budget. Here we assess how emissions from short-lived non-CO 2 species like methane, hydrofluorocarbons (HFCs), black-carbon, and sulphates influence these CO 2 budgets. Our default case, which assumes mitigation in all sectors and of all gases, results in a CO 2 budget between 2011–2100 of 340 PgC for a >66% chance of staying below 2°C, consistent with the assessment of the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Extreme variations of air-pollutant emissions from black-carbon and sulphates influence this budget by about ±5%. In the hypothetical case of no methane or HFCs mitigation—which is unlikely when CO 2 is stringently reduced—the budgets would be much smaller (40% or up to 60%, respectively). However, assuming very stringent CH 4 mitigation as a sensitivity case, CO 2 budgets could be 25% higher. A limit on cumulative CO 2 emissions remains critical for temperature targets. Even a 25% higher CO 2 budget still means peaking global emissions in the next two decades, and achieving net zero CO 2 emissions during the third quarter of the 21st century. The leverage we have to affect the CO 2 budget by targeting non-CO 2 diminishes strongly along with CO 2 mitigation, because these are partly linked through economic and technological factors. (letter)

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

Air-sea exchanges of materials in the Indian Ocean: Concerns and strategies

Digital Repository Service at National Institute of Oceanography (India)

DileepKumar, M.

biological production is entirely due to leakage of agricultural effluents into coastal waters, as the present knowledge on the seasonal variability of nutrients and biological production in waters along the Indian coast is still limited. If this theory... to gaseous CO2 with minor reduction in pH. The gaseous CO2 in seawater determines the extent of air-sea exchange. But small changes in temperature or pH can modify gaseous CO2 content in seawater. Thus shifts in physico- chemical and biological regimes...

Carbon Dioxide Variability in the Gulf of Trieste (GOT) in the Northern Adriatic Sea

Science.gov (United States)

Turk, D.; McGillis, W. R.; Malacic, V.; Degrandpre, M.

2008-12-01

Coastal marine regions such as the Gulf of Trieste GOT in the Northern Adriatic Sea serve as the link between carbon cycling on land and the ocean interior and potentially contribute large uncertainties in the estimate of anthropogenic CO2 uptake. This system may be either a sink or a source for atmospheric CO2. Understanding the sources and sinks as a result of biological and physical controls for air-sea carbon dioxide fluxes in coastal waters may substantially alter the current view of the global carbon budget for unique terrestrial and ocean regions such as the GOT. GOT is a semi-enclosed Mediterranean basin situated in the northern part of Adriatic Sea. It is one of the most productive regions in the Mediterranean and is affected by extreme fresh river input, phytoplankton blooms, and large changes of air-sea exchange during Bora high wind events. The unique combination of these environmental processes and relatively small size of the area makes the region an excellent study site for investigations of air-sea interaction, and changes in biology and carbon chemistry. However, there is a dearth of current data or information from the region. Here we present the first measurements of air and water CO2 flux in the GOT. The aqueous CO2 was measured at the Coastal Oceanographic buoy Piran, Slovenia using the SAMI CO2 sensor during spring and late summer and fall 2007. CO2 measurements were combined with hydrological and biological observations to evaluate the processes that control carbon cycling in the region.

Influence of travel behavior on global CO2 emissions

NARCIS (Netherlands)

Girod, B.; Vuuren, D.P. van; Vries, B. de

2013-01-01

Travel demand is rising steeply and its contribution to global CO2 emissions is increasing. Different studies have shown possible mitigation through technological options, but so far few studies have evaluated the implications of changing travel behavior on global travel demand, energy use and CO2

Autumn CO2 chemistry in the Japan Sea and the impact of discharges from the Changjiang River

Science.gov (United States)

Kosugi, Naohiro; Sasano, Daisuke; Ishii, Masao; Enyo, Kazutaka; Saito, Shu

2016-08-01

We made comprehensive surface water CO2 chemistry observations in the Japan Sea during each autumn from 2010 to 2014. The partial pressure of CO2 (pCO2) in surface water, 312-329 μatm, was 10-30 μatm lower in the Japan Sea than in the same latitude range of the western North Pacific adjacent to Japan. According to the sensitivity analysis of pCO2, the lower pCO2 in the Japan Sea was primarily attributable to a large seasonal decrease of pCO2 associated with strong cooling in autumn, particularly in the northern Japan Sea. In contrast, the lower pCO2 in relatively warm, freshwater in the southern Japan Sea was attributable to not only the thermodynamic effect of the temperature changes but also high total alkalinity. This alkalinity had its origin in Changjiang River and was transported by Changjiang diluted water (CDW) which seasonally runs into the Japan Sea from the East China Sea. The input of total alkalinity through CDW also elevated the saturation state of calcium carbonate minerals and mitigated the effects of anthropogenic ocean acidification, at least during autumn. These biogeochemical impacts of CDW in the Japan Sea last until November, although the inflow from the East China Sea to the Japan Sea almost ceases by the end of September. The long duration of the high saturation state of calcium carbonate benefits calcareous marine organisms.

Net uptake of atmospheric CO2 by coastal submerged aquatic vegetation

Science.gov (United States)

Tokoro, Tatsuki; Hosokawa, Shinya; Miyoshi, Eiichi; Tada, Kazufumi; Watanabe, Kenta; Montani, Shigeru; Kayanne, Hajime; Kuwae, Tomohiro

2014-01-01

‘Blue Carbon’, which is carbon captured by marine living organisms, has recently been highlighted as a new option for climate change mitigation initiatives. In particular, coastal ecosystems have been recognized as significant carbon stocks because of their high burial rates and long-term sequestration of carbon. However, the direct contribution of Blue Carbon to the uptake of atmospheric CO2 through air-sea gas exchange remains unclear. We performed in situ measurements of carbon flows, including air-sea CO2 fluxes, dissolved inorganic carbon changes, net ecosystem production, and carbon burial rates in the boreal (Furen), temperate (Kurihama), and subtropical (Fukido) seagrass meadows of Japan from 2010 to 2013. In particular, the air-sea CO2 flux was measured using three methods: the bulk formula method, the floating chamber method, and the eddy covariance method. Our empirical results show that submerged autotrophic vegetation in shallow coastal waters can be functionally a sink for atmospheric CO2. This finding is contrary to the conventional perception that most near-shore ecosystems are sources of atmospheric CO2. The key factor determining whether or not coastal ecosystems directly decrease the concentration of atmospheric CO2 may be net ecosystem production. This study thus identifies a new ecosystem function of coastal vegetated systems; they are direct sinks of atmospheric CO2. PMID:24623530

An analysis of warm pool and cold tongue El Ninos: air-sea coupling processes, global influences, and recent trends

Energy Technology Data Exchange (ETDEWEB)

Hu, Zeng-Zhen; Kumar, Arun; Wang, Wanqiu [NCEP/NWS/NOAA, Climate Prediction Center, Camp Springs, MD (United States); Jha, Bhaskar; Huang, Boyin [NCEP/NWS/NOAA, Climate Prediction Center, Camp Springs, MD (United States); Wyle Information Systems, Camp Springs, MD (United States); Huang, Bohua [George Mason University, Department of Atmospheric, Oceanic, and Earth Sciences, College of Science, Fairfax, VA (United States); Center for Ocean-Land-Atmosphere Studies, Calverton, MD (United States)

2012-05-15

The differences in tropical air-sea interactions and global climate connection as well as the hindcast skills for the warm pool (WP) and cold tongue (CT) El Ninos are investigated based on observed, (re)analyzed, and model hindcast data. The robustness of observed global climate connection is established from the model simulations. Lastly, variations of atmosphere and ocean conditions in the recent decades, and their possible connection with the frequency increase of the WP El Nino are discussed. Consistent with previous results, our individual case study and composite results suggest that stronger (weaker) and more eastward extended (westward confined) westerly wind along the equatorial Pacific in early months of a year is associated with active (suppressed) air-sea interaction over the cold tongue/the Intertropical Convergence Zone complex, as well as more (less) intensive oceanic thermocline feedback, favoring the CT (WP) El Nino development. The preceding westerly wind signal and air-sea interaction differences may be responsible for the predication skill difference with higher (lower) overall hindcast skill for the CT (WP) El Nino in the Climate Forecast System of National Centers for Environmental Prediction. Our model experiments show that, in addition to the tropics, the eastern Pacific, North America and North Atlantic are the major regions having robust climate differences between the CT and WP El Ninos. Nevertheless, the climate contrasts seem not robust over the Eurasian continent. Also, the frequency increase of the WP El Nino in the recent decades may not be directly connected with the linear trend of the tropical climate. (orig.)

China's transportation energy consumption and CO2 emissions from a global perspective

International Nuclear Information System (INIS)

Yin, Xiang; Chen, Wenying; Eom, Jiyong; Clarke, Leon E.; Kim, Son H.; Patel, Pralit L.; Yu, Sha; Kyle, G. Page

2015-01-01

Rapidly growing energy demand from China's transportation sector in the last two decades have raised concerns over national energy security, local air pollution, and carbon dioxide (CO 2 ) emissions, and there is broad consensus that China's transportation sector will continue to grow in the coming decades. This paper explores the future development of China's transportation sector in terms of service demands, final energy consumption, and CO 2 emissions, and their interactions with global climate policy. This study develops a detailed China transportation energy model that is nested in an integrated assessment model—Global Change Assessment Model (GCAM)—to evaluate the long-term energy consumption and CO 2 emissions of China's transportation sector from a global perspective. The analysis suggests that, without major policy intervention, future transportation energy consumption and CO 2 emissions will continue to rapidly increase and the transportation sector will remain heavily reliant on fossil fuels. Although carbon price policies may significantly reduce the sector's energy consumption and CO 2 emissions, the associated changes in service demands and modal split will be modest, particularly in the passenger transport sector. The analysis also suggests that it is more difficult to decarbonize the transportation sector than other sectors of the economy, primarily owing to its heavy reliance on petroleum products. -- Highlights: •Transport sector in China are analyzed from a global perspective. •Passenger transport turnover reduction and modal shifts is less sensitive to carbon price. •Bio-fuel, electricity and H 2 will play an important role for carbon mitigation in transport sector. •The transport sector is more difficult to decarbonize than other sectors

The impact of elevated CO2 and temperature on grain quality of rice grown under open-air field conditions.

Science.gov (United States)

Jing, Liquan; Wang, Juan; Shen, Shibo; Wang, Yunxia; Zhu, Jianguo; Wang, Yulong; Yang, Lianxin

2016-08-01

Rising atmospheric CO2 is accompanied by global warming. However, interactive effects of elevated CO2 and temperature have not been well studied on grain quality of rice. A japonica cultivar was grown in the field using a free-air CO2 enrichment facility in combination with a canopy air temperature increase system in 2014. The gas fumigation (200 µmol mol(-1) above ambient CO2 ) and temperature increase (1 °C above ambient air temperature) were performed from tillering until maturity. Compared with the control (ambient CO2 and air temperature), elevated CO2 increased grain length and width as well as grain chalkiness but decreased protein concentrations. In contrast, the increase in canopy air temperature had less effect on these parameters except for grain chalkiness. The starch pasting properties of rice flour and taste analysis of cooked rice indicated that the palatability of rice was improved by CO2 and/or temperature elevation, with the combination of the two treatments showing the most significant changes compared with ambient rice. It is concluded that projected CO2 in 2050 may have larger effects on rice grain quality than the projected temperature increase. Although deterioration in milling suitability, grain appearance and nutritional quality can be expected, the taste of cooked rice might be better in the future environment. © 2015 Society of Chemical Industry. © 2015 Society of Chemical Industry.

CO2 and CH4 in sea ice from a subarctic fjord under influence of riverine input

DEFF Research Database (Denmark)

Crabeck, O.; Delille, B.; Thomas, D. N.

2014-01-01

We present CH4 concentration [CH4] and the partial pressure of CO2 (pCO2) in bulk sea ice from subarctic, land-fast sea ice in the Kapisillit fjord, Greenland. The bulk ice [CH4] ranged from 1.8 to 12.1 nmol L−1, which corresponds to a partial pressure range of 3 to 28 ppmv. This is markedly higher......-saturated compared to the atmosphere (390 ppmv). Our study adds to the few existing studies of CH4 and CO2 in sea ice and concludes that sub-arctic sea can be a sink for atmospheric CO2, while being a net source of CH4. Processes related to the freezing and melting of sea ice represents large unknowns...... to the exchange of CO2 but also CH4. It is therefore imperative to assess the consequences of these unknowns through further field campaigns and targeted research under other sea ice conditions at both hemispheres....

Storing CO2 under the North Sea Basin - A key solution for combating climate change

International Nuclear Information System (INIS)

Skogen, T; Morris, B; Agerup, M; Svenningsen, S Oe; Kropelien, K F; Solheim, M; Northmore, B; Dixon, T; O'Carroll, K; Greaves, A; Golder, J; Selmer-Olsen, S; Sjoeveit, A; Kaarstad, O; Riley, N; Wright, I; Mansfield, C

2007-06-01

This report represents the first deliverable of the North Sea Basin Task Force, which Norway and the UK established in November 2005 to work together on issues surrounding the transport and storage of CO 2 beneath the North Sea. The North Sea represents the best geological opportunity for storing our CO 2 emissions away from the atmosphere for both the UK and Norway

Do Continental Shelves Act as an Atmospheric CO2 Sink?

Science.gov (United States)

Cai, W.

2003-12-01

Recent air-to-sea CO2 flux measurements at several major continental shelves (European Atlantic Shelves, East China Sea and U.S. Middle Atlantic Bight) suggest that shelves may act as a one-way pump and absorb atmospheric CO2 into the ocean. These observations also favor the argument that continental shelves are autotrophic (i.e., net production of organic carbon, OC). The U.S. South Atlantic Bight (SAB) contrasts these findings in that it acts as a strong source of CO2 to the atmosphere while simultaneously exporting dissolved inorganic carbon (DIC) to the open ocean. We report pCO2, DIC, and alkalinity data from the SAB collected in 8 cruises along a transect from the shore to the shelf break in the central SAB. The shelf-wide net heterotrophy and carbon exports in the SAB are subsidized by the export of OC from the abundant intertidal marshes, which are a sink for atmospheric CO2. It is proposed here that the SAB represents a marsh-dominated heterotrophic ocean margin as opposed to river-dominated autotrophic margins. To further investigate why margins may behave differently in term of CO2 sink/source, the physical and biological conditions of several western boundary current margins are compared. Based on this and other studies, DIC export flux from margins to the open ocean must be significant in the overall global ocean carbon budget.

Gas exchange at the air-sea interface: a technique for radon measurements in seawater

International Nuclear Information System (INIS)

Queirazza, G.; Roveri, M.

1991-01-01

The rate of exchange of various gas species, such as O 2 , CO 2 etc. across the air-water interface can be evaluated from the 222 Rn vertical profiles in the water column. Radon profiles were measured in 4 stations in the NW Adriatic Sea, in September 1990, using solvent extraction and liquid scintillation counting techniques, directly on board the ship. The radiochemical procedure is described in detail. The lower limit of detection is approximately 0.4 mBq 1 -1 . The radon deficiency in the profiles gives estimates of the gas transfer rate across the air-sea interface ranging from 0.9 to 7.0 m d -1 . The suitability of the radon deficiency method in shallow water, enclosed seas is briefly discussed. (Author)

On which timescales do gas transfer velocities control North Atlantic CO2 flux variability?

Science.gov (United States)

Couldrey, Matthew P.; Oliver, Kevin I. C.; Yool, Andrew; Halloran, Paul R.; Achterberg, Eric P.

2016-05-01

The North Atlantic is an important basin for the global ocean's uptake of anthropogenic and natural carbon dioxide (CO2), but the mechanisms controlling this carbon flux are not fully understood. The air-sea flux of CO2, F, is the product of a gas transfer velocity, k, the air-sea CO2 concentration gradient, ΔpCO2, and the temperature- and salinity-dependent solubility coefficient, α. k is difficult to constrain, representing the dominant uncertainty in F on short (instantaneous to interannual) timescales. Previous work shows that in the North Atlantic, ΔpCO2 and k both contribute significantly to interannual F variability but that k is unimportant for multidecadal variability. On some timescale between interannual and multidecadal, gas transfer velocity variability and its associated uncertainty become negligible. Here we quantify this critical timescale for the first time. Using an ocean model, we determine the importance of k, ΔpCO2, and α on a range of timescales. On interannual and shorter timescales, both ΔpCO2 and k are important controls on F. In contrast, pentadal to multidecadal North Atlantic flux variability is driven almost entirely by ΔpCO2; k contributes less than 25%. Finally, we explore how accurately one can estimate North Atlantic F without a knowledge of nonseasonal k variability, finding it possible for interannual and longer timescales. These findings suggest that continued efforts to better constrain gas transfer velocities are necessary to quantify interannual variability in the North Atlantic carbon sink. However, uncertainty in k variability is unlikely to limit the accuracy of estimates of longer-term flux variability.

Removal of CO2 from the terrestrial atmosphere to curtail global warming: From methodology to laboratory prototype

Science.gov (United States)

Orton, Andrea E.

This research has focused on the initial phase of required investigations in pursuit of a global scale methodology for reduction of CO 2 in terrestrial air for the purpose of curtailment of global warming. This methodology was initially presented by Agee, Orton, and Rogers (2013), and has provided the basis for pursuing this thesis research. The first objective of the research project was to design and build a laboratory prototype system, capable of depleting CO2 from terrestrial air at 1 bar of pressure through LN2 refrigeration. Design considerations included a 26.5L cylindrical Pyrex glass sequestration chamber, a container to hold a reservoir of LN2 and an interface between the two to allow for cooling and instrumentation ports for measurements inside the sequestration chamber. Further, consideration was given to the need for appropriate insulating material to enclose the assembled apparatus to help achieve efficient cooling and the threshold depositional temperature of 135 K. The Amy Facility in the Department of Chemistry provided critical expertise to machine the apparatus to specifications, especially the stainless steel interface plate. Research into available insulating materials resulted in the adaption of TRYMER RTM 2500 Polyisocyanurate, effective down to 90 K. The above described DAC prototype designed for CO2 sequestration accomplished two of the initial research objectives investigated: 1) conduct refrigeration experiments to achieve CO2 terrestrial deposition temperature of 135 K (uniformly) and 2) deplete CO2 from the chamber air at 1 bar of pressure, documented by appropriate measurements. It took approximately 5.5 hours for the chamber to be completely uniform in temperature of 135 K (and below) through the use of LN2 poured into the container sitting on an aluminum interface on top of the sequestration Pyrex chamber. As expected, Rayleigh-Taylor instability (more dense fluid over less dense fluid) was observed through the duration of the

Application of free-air CO2 enrichment (FACE) technology to a forest canopy: A simulation study

International Nuclear Information System (INIS)

Lipfert, F.W.; Hendrey, G.R.; Lewin, K.L.; Alexander, Y.

1992-03-01

Forest ecosystems constitute an important part of the planet's land cover. Understanding their exchanges of carbon with the atmosphere is crucial in projecting future net atmospheric CO 2 increases. It is also important that experimental studies of these processes be performed under conditions which are as realistic as possible, particularly with respect to photosynthesis and evapotranspiration. New technology and experimental protocols now exist which can facilitate studying an undisturbed forest canopy under long-term enriched CO 2 conditions. The International Geosphere Biosphere Program of the International Council of Scientific Unions has established a subprogram on Global Change and Terrestrial Ecosystems (GCTE). This program is driven by two major concerns: to be able to predict the effects of global change on the structure and function of ecosystems, and to predict how these changes will control both atmospheric CO 2 and climate, through various feedback pathways. Brookhaven National Laboratory (BNL) has developed a system for exposing field-grown plants to controlled elevated concentrations of atmospheric gases, without use of confining chambers that alter important atmospheric exchange processes. This system, called FACE for Free Air CO 2 Enrichment. This paper focuses on the fluid mechanics of free-air fumigation and uses a numerical simulation model based on superposed gaussian plumes to project how the present ground-based system could be used to fumigate an elevated forest canopy

CO2 emissions driven by wind are produced at global scale

Science.gov (United States)

Rosario Moya, M.; Sánchez-Cañete, Enrique P.; Kowalski, Andrew S.; Serrano-Ortiz, Penélope; López-Ballesteros, Ana; Oyonarte, Cecilio; Domingo, Francisco

2017-04-01

As an important tool for understanding and monitoring ecosystem dynamics at ecosystem level, the eddy covariance (EC) technique allows the assessment of the diurnal and seasonal variation of the net ecosystem exchange (NEE). Despite the high temporal resolution data, there are still many processes (in addition to photosynthesis and respiration) that, although they are being monitored, have been neglected. Only a few authors have studied anomalous CO2 emissions (non biological), and have related them to soil ventilation, photodegradation or geochemical processes. The aims of this study are: 1) to identify anomalous daytime CO2 emissions in different ecosystems distributed around the world, 2) to determine the meteorological variables that influence these emissions, and 3) to explore the potential processes which can be involved. We have studied EC data together with other meteorological ancillary variables obtained from the FLUXNET database and have found more than 50 sites with anomalous CO2 emissions in different ecosystem types such as grasslands, croplands or savannas. Data were filtered according to the FLUXNET quality control flags (only data with maximum quality were used, i.e. control flag equal to 0) and daytime (shortwave radiation incoming > 50 W m-2). Partial Spearman correlation analyses were performed between NEE and ancillary data: air temperature, vapour pressure deficit, soil temperature, precipitation, atmospheric pressure, soil water content, incoming photosynthetic photon flux density, friction velocity and net radiation. When necessary, ancillary variables were gap-filled using the MDS method (Reichstein et al. 2005). Preliminary results showed strong and highly significant correlations between friction velocity and anomalous CO2 emissions, suggesting that these emissions were mainly produced by ventilation events. Anomalous CO2 emissions were found mainly in arid ecosystems and sites with hot and dry summers. We suggest that anomalous CO2

Growth strategy of Norway spruce under air elevated [CO2

Science.gov (United States)

Pokorny, R.; Urban, O.; Holisova, P.; Sprtova, M.; Sigut, L.; Slipkova, R.

2012-04-01

Plants will respond to globally increasing atmospheric CO2 concentration ([CO2]) by acclimation or adaptation at physiological and morphological levels. Considering the temporal onset, physiological responses may be categorized as short-term and morphological ones as long-term responses. The degree of plant growth responses, including cell division and cell expansion, is highly variable. It depends mainly on the specie's genetic predisposition, environment, mineral nutrition status, duration of CO2 enrichment, and/or synergetic effects of other stresses. Elevated [CO2] causes changes in tissue anatomy, quantity, size, shape and spatial orientation and can result in altered sink strength. Since, there are many experimental facilities for the investigation of elevated [CO2] effects on trees: i) closed systems or open top chambers (OTCs), ii) semi-open systems (for example glass domes with adjustable lamella windows - DAWs), and iii) free-air [CO2] enrichments (FACE); the results are still unsatisfactory due to: i) relatively short-term duration of experiments, ii) cultivation of young plants with different growth strategy comparing to old ones, iii) plant cultivation under artificial soil and weather conditions, and iv) in non-representative stand structure. In this contribution we are discussing the physiological and morphological responses of Norway spruce trees cultivated in DAWs during eight consecutive growing seasons in the context with other results from Norway spruce cultivation under air-elevated [CO2] conditions. On the level of physiological responses, we discuss the changes in the rate of CO2 assimilation, assimilation capacity, photorespiration, dark respiration, stomatal conductance, water potential and transpiration, and the sensitivity of these physiological processes to temperature. On the level of morphological responses, we discuss the changes in bud and growth phenology, needle and shoot morphology, architecture of crown and root system, wood

Panorama 2013 - Air transport and the problem of CO2: ETS mechanisms and bio-jet fuels

International Nuclear Information System (INIS)

Jean-Francois Gruson

2013-01-01

Air transport currently accounts for only 2% (∼600 Mt/year) of global CO 2 emissions from human activity. Despite this 2% level, this industry is targeted by governments - especially European Union - and initiatives targeting zero growth in carbon from 2020 onwards, and a 50% reduction by 2050. Over and above aircraft technical innovations and the way in which air traffic is organised, the introduction of ETS (Emissions Trading System) mechanisms and the development of bio-jet fuels are the options most commonly cited in discussions on how to achieve that target. (author)

Air–sea fluxes of CO2 and CH4 from the Penlee Point Atmospheric Observatory on the south-west coast of the UK

Directory of Open Access Journals (Sweden)

M. Yang

2016-05-01

Full Text Available We present air–sea fluxes of carbon dioxide (CO2, methane (CH4, momentum, and sensible heat measured by the eddy covariance method from the recently established Penlee Point Atmospheric Observatory (PPAO on the south-west coast of the United Kingdom. Measurements from the south-westerly direction (open water sector were made at three different sampling heights (approximately 15, 18, and 27 m above mean sea level, a.m.s.l., each from a different period during 2014–2015. At sampling heights  ≥  18 m a.m.s.l., measured fluxes of momentum and sensible heat demonstrate reasonable ( ≤  ±20 % in the mean agreement with transfer rates over the open ocean. This confirms the suitability of PPAO for air–sea exchange measurements in shelf regions. Covariance air–sea CO2 fluxes demonstrate high temporal variability. Air-to-sea transport of CO2 declined from spring to summer in both years, coinciding with the breakdown of the spring phytoplankton bloom. We report, to the best of our knowledge, the first successful eddy covariance measurements of CH4 emissions from a marine environment. Higher sea-to-air CH4 fluxes were observed during rising tides (20 ± 3; 38 ± 3; 29 ± 6 µmole m−2 d−1 at 15, 18, 27 m a.m.s.l. than during falling tides (14 ± 2; 22 ± 2; 21 ± 5 µmole m−2 d−1, consistent with an elevated CH4 source from an estuarine outflow driven by local tidal circulation. These fluxes are a few times higher than the predicted CH4 emissions over the open ocean and are significantly lower than estimates from other aquatic CH4 hotspots (e.g. polar regions, freshwater. Finally, we found the detection limit of the air–sea CH4 flux by eddy covariance to be 20 µmole m−2 d−1 over hourly timescales (4 µmole m−2 d−1 over 24 h.

Precession and atmospheric CO2 modulated variability of sea ice in the central Okhotsk Sea since 130,000 years ago

Science.gov (United States)

Lo, Li; Belt, Simon T.; Lattaud, Julie; Friedrich, Tobias; Zeeden, Christian; Schouten, Stefan; Smik, Lukas; Timmermann, Axel; Cabedo-Sanz, Patricia; Huang, Jyh-Jaan; Zhou, Liping; Ou, Tsong-Hua; Chang, Yuan-Pin; Wang, Liang-Chi; Chou, Yu-Min; Shen, Chuan-Chou; Chen, Min-Te; Wei, Kuo-Yen; Song, Sheng-Rong; Fang, Tien-Hsi; Gorbarenko, Sergey A.; Wang, Wei-Lung; Lee, Teh-Quei; Elderfield, Henry; Hodell, David A.

2018-04-01

Recent reduction in high-latitude sea ice extent demonstrates that sea ice is highly sensitive to external and internal radiative forcings. In order to better understand sea ice system responses to external orbital forcing and internal oscillations on orbital timescales, here we reconstruct changes in sea ice extent and summer sea surface temperature (SSST) over the past 130,000 yrs in the central Okhotsk Sea. We applied novel organic geochemical proxies of sea ice (IP25), SSST (TEX86L) and open water marine productivity (a tri-unsaturated highly branched isoprenoid and biogenic opal) to marine sediment core MD01-2414 (53°11.77‧N, 149°34.80‧E, water depth 1123 m). To complement the proxy data, we also carried out transient Earth system model simulations and sensitivity tests to identify contributions of different climatic forcing factors. Our results show that the central Okhotsk Sea was ice-free during Marine Isotope Stage (MIS) 5e and the early-mid Holocene, but experienced variable sea ice cover during MIS 2-4, consistent with intervals of relatively high and low SSST, respectively. Our data also show that the sea ice extent was governed by precession-dominated insolation changes during intervals of atmospheric CO2 concentrations ranging from 190 to 260 ppm. However, the proxy record and the model simulation data show that the central Okhotsk Sea was near ice-free regardless of insolation forcing throughout the penultimate interglacial, and during the Holocene, when atmospheric CO2 was above ∼260 ppm. Past sea ice conditions in the central Okhotsk Sea were therefore strongly modulated by both orbital-driven insolation and CO2-induced radiative forcing during the past glacial/interglacial cycle.

CO{sub 2} threshold for millennial-scale oscillations in the climate system: implications for global warming scenarios

Energy Technology Data Exchange (ETDEWEB)

Meissner, Katrin J.; Eby, Michael; Weaver, Andrew J. [University of Victoria, School of Earth and Ocean Sciences, Victoria, BC (Canada); Saenko, Oleg A. [Canadian Centre for Climate Modelling and Analysis, Victoria (Canada)

2008-02-15

We present several equilibrium runs under varying atmospheric CO{sub 2} concentrations using the University of Victoria Earth System Climate Model (UVic ESCM). The model shows two very different responses: for CO{sub 2} concentrations of 400 ppm or lower, the system evolves into an equilibrium state. For CO{sub 2} concentrations of 440 ppm or higher, the system starts oscillating between a state with vigorous deep water formation in the Southern Ocean and a state with no deep water formation in the Southern Ocean. The flushing events result in a rapid increase in atmospheric temperatures, degassing of CO{sub 2} and therefore an increase in atmospheric CO{sub 2} concentrations, and a reduction of sea ice cover in the Southern Ocean. They also cool the deep ocean worldwide. After the flush, the deep ocean warms slowly again and CO{sub 2} is taken up by the ocean until the stratification becomes unstable again at high latitudes thousands of years later. The existence of a threshold in CO{sub 2} concentration which places the UVic ESCM in either an oscillating or non-oscillating state makes our results intriguing. If the UVic ESCM captures a mechanism that is present and important in the real climate system, the consequences would comprise a rapid increase in atmospheric carbon dioxide concentrations of several tens of ppm, an increase in global surface temperature of the order of 1-2 C, local temperature changes of the order of 6 C and a profound change in ocean stratification, deep water temperature and sea ice cover. (orig.)

Regulation of CO2 Air Sea Fluxes by Sediments in the North Sea

Science.gov (United States)

Burt, William; Thomas, Helmuth; Hagens, Mathilde; Brenner, Heiko; Pätsch, Johannes; Clargo, Nicola; Salt, Lesley

2016-04-01

A multi-tracer approach is applied to assess the impact of boundary fluxes (e.g. benthic input from sediments or lateral inputs from the coastline) on the acid-base buffering capacity, and overall biogeochemistry, of the North Sea. Analyses of both basin-wide observations in the North Sea and transects through tidal basins at the North-Frisian coastline, reveal that surface distributions of the δ13C signature of dissolved inorganic carbon (DIC) are predominantly controlled by a balance between biological production and respiration. In particular, variability in metabolic DIC throughout stations in the well-mixed southern North Sea indicates the presence of an external carbon source, which is traced to the European continental coastline using naturally-occurring radium isotopes (224Ra and 228Ra). 228Ra is also shown to be a highly effective tracer of North Sea total alkalinity (AT) compared to the more conventional use of salinity. Coastal inputs of metabolic DIC and AT are calculated on a basin-wide scale, and ratios of these inputs suggest denitrification as a primary metabolic pathway for their formation. The AT input paralleling the metabolic DIC release prevents a significant decline in pH as compared to aerobic (i.e. unbuffered) release of metabolic DIC. Finally, long-term pH trends mimic those of riverine nitrate loading, highlighting the importance of coastal AT production via denitrification in regulating pH in the southern North Sea.

Global temperature definition affects achievement of long-term climate goals

Science.gov (United States)

Richardson, Mark; Cowtan, Kevin; Millar, Richard J.

2018-05-01

The Paris Agreement on climate change aims to limit ‘global average temperature’ rise to ‘well below 2 °C’ but reported temperature depends on choices about how to blend air and water temperature data, handle changes in sea ice and account for regions with missing data. Here we use CMIP5 climate model simulations to estimate how these choices affect reported warming and carbon budgets consistent with the Paris Agreement. By the 2090s, under a low-emissions scenario, modelled global near-surface air temperature rise is 15% higher (5%–95% range 6%–21%) than that estimated by an approach similar to the HadCRUT4 observational record. The difference reduces to 8% with global data coverage, or 4% with additional removal of a bias associated with changing sea-ice cover. Comparison of observational datasets with different data sources or infilling techniques supports our model results regarding incomplete coverage. From high-emission simulations, we find that a HadCRUT4 like definition means higher carbon budgets and later exceedance of temperature thresholds, relative to global near-surface air temperature. 2 °C warming is delayed by seven years on average, to 2048 (2035–2060), and CO2 emissions budget for a >50% chance of <2 °C warming increases by 67 GtC (246 GtCO2).

A rapid transition from ice covered CO2–rich waters to a biologically mediated CO2 sink in the eastern Weddell Gyre

Directory of Open Access Journals (Sweden)

W. Geibert

2008-09-01

Full Text Available Circumpolar Deep Water (CDW, locally called Warm Deep Water (WDW, enters the Weddell Gyre in the southeast, roughly at 25° E to 30° E. In December 2002 and January 2003 we studied the effect of entrainment of WDW on the fugacity of carbon dioxide (fCO2 and dissolved inorganic carbon (DIC in Weddell Sea surface waters. Ultimately the fCO2 difference across the sea surface drives air-sea fluxes of CO2. Deep CTD sections and surface transects of fCO2 were made along the Prime Meridian, a northwest-southeast section, and along 17° E to 23° E during cruise ANT XX/2 on FS Polarstern. Upward movement and entrainment of WDW into the winter mixed layer had significantly increased DIC and fCO2 below the sea ice along 0° W and 17° E to 23° E, notably in the southern Weddell Gyre. Nonetheless, the ice cover largely prevented outgassing of CO2 to the atmosphere. During and upon melting of the ice, biological activity rapidly reduced surface water fCO2 by up to 100 μatm, thus creating a sink for atmospheric CO2. Despite the tendency of the surfacing WDW to cause CO2 supersaturation, the Weddell Gyre may well be a CO2 sink on an annual basis due to this effective mechanism involving ice cover and ensuing biological fCO2 reduction. Dissolution of calcium carbonate (CaCO3 in melting sea ice may play a minor role in this rapid reduction of surface water fCO2.

Crop responses to CO2 enrichment

International Nuclear Information System (INIS)

Rogers, H.H.; Dahlman, R.C.

1993-01-01

Carbon dioxide is rising in the global atmosphere, and this increase can be expected to continue into the foreseeable future. This compound is an essential input to plant life. Crop function is affected across all scales from biochemical to agroecosystem. An array of methods (leaf cuvettes, field chambers, free-air release systems) are available for experimental studies of CO 2 effects. Carbon dioxide enrichment of the air in which crops grow usually stimulates their growth and yield. Plant structure and physiology are markedly altered. Interactions between CO 2 and environmental factors that influence plants are known to occur. Implications for crop growth and yield are enormous. Strategies designed to assure future global food security must include a consideration of crop responses to elevated atmospheric CO 2 . 137 refs., 4 figs., 4 tabs

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.

CO2 is in the air. Five myths about the role of air transport in climate changes

International Nuclear Information System (INIS)

2015-12-01

This publication discusses and criticises some general opinions on air transport. Thus, it is often said that air transport is a minor contributor to greenhouse effect (whereas air transport emits as much CO 2 as Germany who is the sixth World emitter, and has various impacts on health), that air transport is doing a lot for the climate (whereas it in fact manages not to be affected by policies against climate change), that more air passengers result in less CO 2 (whereas traffic predictions would result in an increased oil consumption, and increased CO 2 emissions despite promised technological improvements), that technical progress is at the service of climate (whereas the sector is notably late to reach its defined objectives in terms of energy efficiency), and that air transport is the only way to travel (whereas other means emit much less CO 2 ). Some recommendations are made for measures to be adopted at the international, European and French levels for a better protection of the environment

Net radiative forcing and air quality responses to regional CO emission reductions

Directory of Open Access Journals (Sweden)

M. M. Fry

2013-05-01

Full Text Available Carbon monoxide (CO emissions influence global and regional air quality and global climate change by affecting atmospheric oxidants and secondary species. We simulate the influence of halving anthropogenic CO emissions globally and individually from 10 regions on surface and tropospheric ozone, methane, and aerosol concentrations using a global chemical transport model (MOZART-4 for the year 2005. Net radiative forcing (RF is then estimated using the GFDL (Geophysical Fluid Dynamics Laboratory standalone radiative transfer model. We estimate that halving global CO emissions decreases global annual average concentrations of surface ozone by 0.45 ppbv, tropospheric methane by 73 ppbv, and global annual net RF by 36.1 mW m−2, nearly equal to the sum of changes from the 10 regional reductions. Global annual net RF per unit change in emissions and the 100 yr global warming potential (GWP100 are estimated as −0.124 mW m−2 (Tg CO−1 and 1.34, respectively, for the global CO reduction, and ranging from −0.115 to −0.131 mW m−2 (Tg CO−1 and 1.26 to 1.44 across 10 regions, with the greatest sensitivities for regions in the tropics. The net RF distributions show widespread cooling corresponding to the O3 and CH4 decreases, and localized positive and negative net RFs due to changes in aerosols. The strongest annual net RF impacts occur within the tropics (28° S–28° N followed by the northern midlatitudes (28° N–60° N, independent of reduction region, while the greatest changes in surface CO and ozone concentrations occur within the reduction region. Some regional reductions strongly influence the air quality in other regions, such as East Asia, which has an impact on US surface ozone that is 93% of that from North America. Changes in the transport of CO and downwind ozone production clearly exceed the direct export of ozone from each reduction region. The small variation in CO GWPs among world regions suggests that future international

Storing CO{sub 2} under the North Sea Basin - A key solution for combating climate change

Energy Technology Data Exchange (ETDEWEB)

Skogen, T; Morris, B; Agerup, M; Svenningsen, S Oe; Kropelien, K F; Solheim, M; Northmore, B; Dixon, T; O' Carroll, K; Greaves, A; Golder, J; Selmer-Olsen, S; Sjoeveit, A; Kaarstad, O; Riley, N; Wright, I; Mansfield, C

2007-06-15

This report represents the first deliverable of the North Sea Basin Task Force, which Norway and the UK established in November 2005 to work together on issues surrounding the transport and storage of CO{sub 2} beneath the North Sea. The North Sea represents the best geological opportunity for storing our CO{sub 2} emissions away from the atmosphere for both the UK and Norway

Aircraft measurements of SO2, NOx, CO, and O3 over the coastal and offshore area of Yellow Sea of China.

Science.gov (United States)

Yang, Xiaoyang; Wang, Xinhua; Yang, Wen; Xu, Jun; Ren, Lihong; He, Youjiang; Liu, Bing; Bai, Zhipeng; Meng, Fan; Hu, Min

2016-09-01

In order to investigate long-range transport of the air pollution in the East Asia, air pollutants, including SO2, NOx, CO, and O3, were observed by aircraft measurement over the coastal and offshore area of Yellow Sea of China in April 2011. NOx and SO2 seemed to become moderate in recent years, and the concentrations during the whole observations ranged from 0.49 to 9.57 ppb and from 0.10 to 16.02 ppb, respectively. The high concentrations of CO were measured with an average value of 0.98 ppm. The measured O3 average concentration was 76.25 ppb, which showed a higher level comparing with the results from some previous studies. Most of the results for the concentration values generally followed the typical characteristic of vertical and spatial distribution, which were "low altitude > high altitude" and "land/coastal > sea," respectively. Transport of polluted air mass from the continent to the aircraft measurement area was confirmed in some days during the observation by the meteorological analysis, while the measurement results supposed to represent the background level of the pollutants in rest days. Additionally, some small-scale air pollution plumes were observed. Significant positive correlations between NOx and SO2 indicated that these two species originated from the same region. On the other hand, good positive correlations between NOx and O3 found during 2-day flight suggested that the O3 formation was probably under "NOx-limited" regime in these days.

Observational analysis of air-sea fluxes and sea water temperature offshore South China Sea

Science.gov (United States)

Bi, X.; Huang, J.; Gao, Z.; Liu, Y.

2017-12-01

This paper investigates the air-sea fluxes (momentum flux, sensible heat flux and latent heat flux) from eddy covariance method based on data collected at an offshore observation tower in the South China Sea from January 2009 to December 2016 and sea water temperature (SWT) on six different levels based on data collected from November 2011 to June 2013. The depth of water at the tower over the sea averages about 15 m. This study presents the in-situ measurements of continuous air-sea fluxes and SWT at different depths. Seasonal and diurnal variations in air-sea fluxes and SWT on different depths are examined. Results show that air-sea fluxes and all SWT changed seasonally; sea-land breeze circulation appears all the year round. Unlike winters where SWT on different depths are fairly consistent, the difference between sea surface temperature (SST) and sea temperature at 10 m water depth fluctuates dramatically and the maximum value reaches 7 °C during summer.

Tidal influence on the sea-to-air transfer of CH4 in the coastal ocean

International Nuclear Information System (INIS)

Hahm, Doshik; Kim, Guebuem; Lee, Yong-Woo; Nam, Sungh-Yun; Kim, Kyung-Ryul; Kim, Kuh

2006-01-01

We obtained real-time monitoring data of water temperature, salinity, wind, current, CH 4 and other oceanographic parameters in a coastal bay in the southern sea of Korea from July 8 to August 15, 2003, using an environmental monitoring buoy. In general, the transfer velocity of environmental gases across the air-sea interface is obtained exclusively from empirical relationships with wind speeds. However, our monitoring data demonstrate that the agitation of the aqueous boundary layer is controlled significantly by tidal turbulence, similar to the control exercised by wind stress in the coastal ocean. The sea-to-air transfer of CH 4 is enhanced significantly during spring tide due to an increase in the gas transfer velocity and vertical CH 4 transport from bottom water to the surface layer. Thus, our unique time-series results imply that the sea-to-air transfer of gases, such as CH 4 , DMS, DMHg, N 2 O, CO 2 and 222 Rn, from highly enriched coastal bottom waters, is controlled not only by episodic wind events but also by regular tidal turbulence in the coastal ocean

Variability of North Sea pH and CO2 in response to North Atlantic Oscillation forcing

DEFF Research Database (Denmark)

Salt, Lesley A.; Thomas, Helmuth; Prowe, Friederike

2013-01-01

[1] High biological activity causes a distinct seasonality of surface water pH in the North Sea, which is a strong sink for atmospheric CO2 via an effective shelf pump. The intimate connection between the North Sea and the North Atlantic Ocean suggests that the variability of the CO2 system...... of the North Atlantic Ocean may, in part, be responsible for the observed variability of pH and CO2 in the North Sea. In this work, we demonstrate the role of the North Atlantic Oscillation (NAO), the dominant climate mode for the North Atlantic, in governing this variability. Based on three extensive...... observational records covering the relevant levels of the NAO index, we provide evidence that the North Sea pH and CO2 system strongly responds to external and internal expressions of the NAO. Under positive NAO, the higher rates of inflow of water from the North Atlantic Ocean and the Baltic outflow lead...

Distributions and sea-to-air fluxes of chloroform, trichloroethylene, tetrachloroethylene, chlorodibromomethane and bromoform in the Yellow Sea and the East China Sea during spring

International Nuclear Information System (INIS)

He, Zhen; Yang, Gui-Peng; Lu, Xiao-Lan; Zhang, Hong-Hai

2013-01-01

Halocarbons including chloroform (CHCl 3 ), trichloroethylene (C 2 HCl 3 ), tetrachloroethylene (C 2 Cl 4 ), chlorodibromomethane (CHBr 2 Cl) and bromoform (CHBr 3 ) were measured in the Yellow Sea (YS) and the East China Sea (ECS) during spring 2011. The influences of chlorophyll a, salinity and nutrients on the distributions of these gases were examined. Elevated levels of these gases in the coastal waters were attributed to anthropogenic inputs and biological release by phytoplankton. The vertical distributions of these gases in the water column were controlled by different source strengths and water masses. Using atmospheric concentrations measured in spring 2012 and seawater concentrations obtained from this study, the sea-to-air fluxes of these gases were estimated. Our results showed that the emissions of C 2 HCl 3 , C 2 Cl 4, CHBr 2 Cl, and CHBr 3 from the study area could account for 16.5%, 10.5%, 14.6%, and 3.5% of global oceanic emissions, respectively, indicating that the coastal shelf may contribute significantly to the global oceanic emissions of these gases. -- Highlights: ► Distributions of the VHCs were studied in the YS and the ECS. ► Elevated levels of VHCs were related to terrestrial input from the Yangtze River. ► Biogenic production from diatoms was an important source of the VHCs. ► Shelf seas could significantly contribute to the global oceanic VHCs emission. -- The elevated levels of the volatile halocarbons in the coastal waters were attributed to anthropogenic inputs and biological release by phytoplankton (e.g., diatoms)

How reversible is sea ice loss?

Directory of Open Access Journals (Sweden)

J. K. Ridley

2012-02-01

Full Text Available It is well accepted that increasing atmospheric CO₂ results in global warming, leading to a decline in polar sea ice area. Here, the specific question of whether there is a tipping point in the sea ice cover is investigated. The global climate model HadCM3 is used to map the trajectory of sea ice area under idealised scenarios. The atmospheric CO₂ is first ramped up to four times pre-industrial levels (4 × CO₂, then ramped down to pre-industrial levels. We also examine the impact of stabilising climate at 4 × CO₂ prior to ramping CO₂ down to pre-industrial levels. Against global mean temperature, Arctic sea ice area is reversible, while the Antarctic sea ice shows some asymmetric behaviour – its rate of change slower, with falling temperatures, than its rate of change with rising temperatures. However, we show that the asymmetric behaviour is driven by hemispherical differences in temperature change between transient and stabilisation periods. We find no irreversible behaviour in the sea ice cover.

Understanding the Role of Air-Sea Interaction on Extreme Rainfall in Aquaplanet and Earth-like CESM2

Science.gov (United States)

Benedict, J. J.; Clement, A. C.; Medeiros, B.

2017-12-01

Extreme precipitation events are associated with anomalous, latitudinally dependent dynamical and convective weather systems. For example, plumes of excessive poleward water vapor transport and topographical effects drive extreme precipitation events in the midlatitudes, while intense tropical precipitation is associated with organized convective systems. In both cases, air-sea fluxes have the potential to contribute significantly to the moisture budget of these storms, but the roles of surface fluxes and upper-ocean processes and their impact on precipitation extremes have yet to be explored in sufficient detail. To examine such mechanisms, we implement a climate model hierarchy that encompasses a spectrum of ocean models, from prescribed-SST to fully dynamic, as well as both aquaplanet and Earth-like lower boundary types within version 2 of the Community Earth System Model (CESM2). Using the CESM2 hierarchy and comparing to observations, we identify key moisture processes and related air-sea interactions that drive extreme precipitation events across different latitudes in Earth-like models and then generalize the analyses in aquaplanet configurations to highlight the most salient features. The analyses are applied to both present-day and global warming conditions to investigate how these fundamental mechanisms might change extreme precipitation events in the future climate.

The relative contributions of biological and abiotic processes to carbon dynamics in subarctic sea ice

DEFF Research Database (Denmark)

Søgaard, Dorte Haubjerg; Thomas, David; Rysgaard, Søren

2013-01-01

Knowledge on the relative effects of biological activity and precipitation/dissolution of calcium carbonate (CaCO3) in influencing the air-ice CO2 exchange in sea-ice-covered season is currently lacking. Furthermore, the spatial and temporal occurrence of CaCO3 and other biogeochemical parameters...... in sea ice are still not well described. Here we investigated autotrophic and heterotrophic activity as well as the precipitation/dissolution of CaCO3 in subarctic sea ice in South West Greenland. Integrated over the entire ice season (71 days), the sea ice was net autotrophic with a net carbon fixation...... and CaCO3 precipitation. The net biological production could only explain 4 % of this sea-ice-driven CO2 uptake. Abiotic processes contributed to an air-sea CO2 uptake of 1.5 mmol m(-2) sea ice day(-1), and dissolution of CaCO3 increased the air-sea CO2 uptake by 36 % compared to a theoretical estimate...

The multimillennial sea-level commitment of global warming.

Science.gov (United States)

Levermann, Anders; Clark, Peter U; Marzeion, Ben; Milne, Glenn A; Pollard, David; Radic, Valentina; Robinson, Alexander

2013-08-20

Global mean sea level has been steadily rising over the last century, is projected to increase by the end of this century, and will continue to rise beyond the year 2100 unless the current global mean temperature trend is reversed. Inertia in the climate and global carbon system, however, causes the global mean temperature to decline slowly even after greenhouse gas emissions have ceased, raising the question of how much sea-level commitment is expected for different levels of global mean temperature increase above preindustrial levels. Although sea-level rise over the last century has been dominated by ocean warming and loss of glaciers, the sensitivity suggested from records of past sea levels indicates important contributions should also be expected from the Greenland and Antarctic Ice Sheets. Uncertainties in the paleo-reconstructions, however, necessitate additional strategies to better constrain the sea-level commitment. Here we combine paleo-evidence with simulations from physical models to estimate the future sea-level commitment on a multimillennial time scale and compute associated regional sea-level patterns. Oceanic thermal expansion and the Antarctic Ice Sheet contribute quasi-linearly, with 0.4 m °C(-1) and 1.2 m °C(-1) of warming, respectively. The saturation of the contribution from glaciers is overcompensated by the nonlinear response of the Greenland Ice Sheet. As a consequence we are committed to a sea-level rise of approximately 2.3 m °C(-1) within the next 2,000 y. Considering the lifetime of anthropogenic greenhouse gases, this imposes the need for fundamental adaptation strategies on multicentennial time scales.

Simultaneously reducing CO2 and particulate exposures via fractional recirculation of vehicle cabin air.

Science.gov (United States)

Jung, Heejung S; Grady, Michael L; Victoroff, Tristan; Miller, Arthur L

2017-07-01

Prior studies demonstrate that air recirculation can reduce exposure to nanoparticles in vehicle cabins. However when people occupy confined spaces, air recirculation can lead to carbon dioxide (CO 2 ) accumulation which can potentially lead to deleterious effects on cognitive function. This study proposes a fractional air recirculation system for reducing nanoparticle concentration while simultaneously suppressing CO 2 levels in the cabin. Several recirculation scenarios were tested using a custom-programmed HVAC (heat, ventilation, air conditioning) unit that varied the recirculation door angle in the test vehicle. Operating the recirculation system with a standard cabin filter reduced particle concentrations to 1000 particles/cm 3 , although CO 2 levels rose to 3000 ppm. When as little as 25% fresh air was introduced (75% recirculation), CO 2 levels dropped to 1000 ppm, while particle concentrations remained below 5000 particles/cm 3 . We found that nanoparticles were removed selectively during recirculation and demonstrated the trade-off between cabin CO 2 concentration and cabin particle concentration using fractional air recirculation. Data showed significant increases in CO 2 levels during 100% recirculation. For various fan speeds, recirculation fractions of 50-75% maintained lower CO 2 levels in the cabin, while still reducing particulate levels. We recommend fractional recirculation as a simple method to reduce occupants' exposures to particulate matter and CO 2 in vehicles. A design with several fractional recirculation settings could allow air exchange adequate for reducing both particulate and CO 2 exposures. Developing this technology could lead to reductions in airborne nanoparticle exposure, while also mitigating safety risks from CO 2 accumulation.

Nitrogen fertilization raises CO2 efflux from inorganic carbon: A global assessment.

Science.gov (United States)

Zamanian, Kazem; Zarebanadkouki, Mohsen; Kuzyakov, Yakov

2018-03-25

Nitrogen (N) fertilization is an indispensable agricultural practice worldwide, serving the survival of half of the global population. Nitrogen transformation (e.g., nitrification) in soil as well as plant N uptake releases protons and increases soil acidification. Neutralizing this acidity in carbonate-containing soils (7.49 × 10 9  ha; ca. 54% of the global land surface area) leads to a CO 2 release corresponding to 0.21 kg C per kg of applied N. We here for the first time raise this problem of acidification of carbonate-containing soils and assess the global CO 2 release from pedogenic and geogenic carbonates in the upper 1 m soil depth. Based on a global N-fertilization map and the distribution of soils containing CaCO 3 , we calculated the CO 2 amount released annually from the acidification of such soils to be 7.48 × 10 12  g C/year. This level of continuous CO 2 release will remain constant at least until soils are fertilized by N. Moreover, we estimated that about 273 × 10 12  g CO 2 -C are released annually in the same process of CaCO 3 neutralization but involving liming of acid soils. These two CO 2 sources correspond to 3% of global CO 2 emissions by fossil fuel combustion or 30% of CO 2 by land-use changes. Importantly, the duration of CO 2 release after land-use changes usually lasts only 1-3 decades before a new C equilibrium is reached in soil. In contrast, the CO 2 released by CaCO 3 acidification cannot reach equilibrium, as long as N fertilizer is applied until it becomes completely neutralized. As the CaCO 3 amounts in soils, if present, are nearly unlimited, their complete dissolution and CO 2 release will take centuries or even millennia. This emphasizes the necessity of preventing soil acidification in N-fertilized soils as an effective strategy to inhibit millennia of CO 2 efflux to the atmosphere. Hence, N fertilization should be strictly calculated based on plant-demand, and overfertilization should be avoided not only

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

Elevated CO2 effects on canopy and soil water flux parameters measured using a large chamber in crops grown with free-air CO2 enrichment.

Science.gov (United States)

Burkart, S; Manderscheid, R; Wittich, K-P; Löpmeier, F J; Weigel, H-J

2011-03-01

An arable crop rotation (winter barley-sugar beet-winter wheat) was exposed to elevated atmospheric CO(2) concentrations ([CO(2) ]) using a FACE facility (Free-Air CO(2) Enrichment) during two rotation periods. The atmospheric [CO(2) ] of the treatment plots was elevated to 550 ppm during daylight hours (T>5°C). Canopy transpiration (E(C) ) and conductance (G(C) ) were measured at selected intervals (>10% of total growing season) using a dynamic CO(2) /H(2) O chamber measuring system. Plant available soil water content (gravimetry and TDR probes) and canopy microclimate conditions were recorded in parallel. Averaged across both growing seasons, elevated [CO(2) ] reduced E(C) by 9%, 18% and 12%, and G(C) by 9%, 17% and 12% in barley, sugar beet and wheat, respectively. Both global radiation (Rg) and vapour pressure deficit (VPD) were the main driving forces of E(C) , whereas G(C) was mostly related to Rg. The responses of E(C) and especially G(C) to [CO(2) ] enrichment were insensitive to weather conditions and leaf area index. However, differences in LAI between plots counteracted the [CO(2) ] impact on E(C) and thus, at least in part, explained the variability of seasonal [CO(2) ] responses between crops and years. As a consequence of lower transpirational canopy water loss, [CO(2) ] enrichment increased plant available soil water content in the course of the season by ca. 15 mm. This was true for all crops and years. Lower transpirational cooling due to a [CO(2) ]-induced reduction of E(C) increased canopy surface and air temperature by up to 2 °C and 0.5 °C, respectively. This is the first study to address effects of FACE on both water fluxes at canopy scale and water status of a European crop rotation. © 2010 German Botanical Society and The Royal Botanical Society of the Netherlands.

An updated observation-based global monthly gridded sea surface pCO2 and air-sea CO2 flux product from 1982 through 2015 and its monthly climatology (NCEI Accession 0160558)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — The observation-based pCO2 fields were created using a 2-step neural network method extensively described and validated in Landschützer et al. 2013, 2014, 2016. The...

Statistical analysis of global surface temperature and sea level using cointegration methods

DEFF Research Database (Denmark)

Schmidt, Torben; Johansen, Søren; Thejll, Peter

2012-01-01

Global sea levels are rising which is widely understood as a consequence of thermal expansion and melting of glaciers and land-based ice caps. Due to the lack of representation of ice-sheet dynamics in present-day physically-based climate models being unable to simulate observed sea level trends......, semi-empirical models have been applied as an alternative for projecting of future sea levels. There is in this, however, potential pitfalls due to the trending nature of the time series. We apply a statistical method called cointegration analysis to observed global sea level and land-ocean surface air...... temperature, capable of handling such peculiarities. We find a relationship between sea level and temperature and find that temperature causally depends on the sea level, which can be understood as a consequence of the large heat capacity of the ocean. We further find that the warming episode in the 1940s...

Can Elevated Air [CO2] Conditions Mitigate the Predicted Warming Impact on the Quality of Coffee Bean?

Directory of Open Access Journals (Sweden)

José C. Ramalho

2018-03-01

Full Text Available Climate changes, mostly related to high temperature, are predicted to have major negative impacts on coffee crop yield and bean quality. Recent studies revealed that elevated air [CO2] mitigates the impact of heat on leaf physiology. However, the extent of the interaction between elevated air [CO2] and heat on coffee bean quality was never addressed. In this study, the single and combined impacts of enhanced [CO2] and temperature in beans of Coffea arabica cv. Icatu were evaluated. Plants were grown at 380 or 700 μL CO2 L-1 air, and then submitted to a gradual temperature rise from 25°C up to 40°C during ca. 4 months. Fruits were harvested at 25°C, and in the ranges of 30–35 or 36–40°C, and bean physical and chemical attributes with potential implications on quality were then examined. These included: color, phenolic content, soluble solids, chlorogenic, caffeic and p-coumaric acids, caffeine, trigonelline, lipids, and minerals. Most of these parameters were mainly affected by temperature (although without a strong negative impact on bean quality, and only marginally, if at all, by elevated [CO2]. However, the [CO2] vs. temperature interaction strongly attenuated some of the negative impacts promoted by heat (e.g., total chlorogenic acids, thus maintaining the bean characteristics closer to those obtained under adequate temperature conditions (e.g., soluble solids, caffeic and p-coumaric acids, trigonelline, chroma, Hue angle, and color index, and increasing desirable features (acidity. Fatty acid and mineral pools remained quite stable, with only few modifications due to elevated air [CO2] (e.g., phosphorous and/or heat. In conclusion, exposure to high temperature in the last stages of fruit maturation did not strongly depreciate bean quality, under the conditions of unrestricted water supply and moderate irradiance. Furthermore, the superimposition of elevated air [CO2] contributed to preserve bean quality by modifying and mitigating

Can Elevated Air [CO2] Conditions Mitigate the Predicted Warming Impact on the Quality of Coffee Bean?

Science.gov (United States)

Ramalho, José C.; Pais, Isabel P.; Leitão, António E.; Guerra, Mauro; Reboredo, Fernando H.; Máguas, Cristina M.; Carvalho, Maria L.; Scotti-Campos, Paula; Ribeiro-Barros, Ana I.; Lidon, Fernando J. C.; DaMatta, Fábio M.

2018-01-01

Climate changes, mostly related to high temperature, are predicted to have major negative impacts on coffee crop yield and bean quality. Recent studies revealed that elevated air [CO2] mitigates the impact of heat on leaf physiology. However, the extent of the interaction between elevated air [CO2] and heat on coffee bean quality was never addressed. In this study, the single and combined impacts of enhanced [CO2] and temperature in beans of Coffea arabica cv. Icatu were evaluated. Plants were grown at 380 or 700 μL CO2 L-1 air, and then submitted to a gradual temperature rise from 25°C up to 40°C during ca. 4 months. Fruits were harvested at 25°C, and in the ranges of 30–35 or 36–40°C, and bean physical and chemical attributes with potential implications on quality were then examined. These included: color, phenolic content, soluble solids, chlorogenic, caffeic and p-coumaric acids, caffeine, trigonelline, lipids, and minerals. Most of these parameters were mainly affected by temperature (although without a strong negative impact on bean quality), and only marginally, if at all, by elevated [CO2]. However, the [CO2] vs. temperature interaction strongly attenuated some of the negative impacts promoted by heat (e.g., total chlorogenic acids), thus maintaining the bean characteristics closer to those obtained under adequate temperature conditions (e.g., soluble solids, caffeic and p-coumaric acids, trigonelline, chroma, Hue angle, and color index), and increasing desirable features (acidity). Fatty acid and mineral pools remained quite stable, with only few modifications due to elevated air [CO2] (e.g., phosphorous) and/or heat. In conclusion, exposure to high temperature in the last stages of fruit maturation did not strongly depreciate bean quality, under the conditions of unrestricted water supply and moderate irradiance. Furthermore, the superimposition of elevated air [CO2] contributed to preserve bean quality by modifying and mitigating the heat impact

Can Elevated Air [CO2] Conditions Mitigate the Predicted Warming Impact on the Quality of Coffee Bean?

Science.gov (United States)

Ramalho, José C; Pais, Isabel P; Leitão, António E; Guerra, Mauro; Reboredo, Fernando H; Máguas, Cristina M; Carvalho, Maria L; Scotti-Campos, Paula; Ribeiro-Barros, Ana I; Lidon, Fernando J C; DaMatta, Fábio M

2018-01-01

Climate changes, mostly related to high temperature, are predicted to have major negative impacts on coffee crop yield and bean quality. Recent studies revealed that elevated air [CO 2 ] mitigates the impact of heat on leaf physiology. However, the extent of the interaction between elevated air [CO 2 ] and heat on coffee bean quality was never addressed. In this study, the single and combined impacts of enhanced [CO 2 ] and temperature in beans of Coffea arabica cv. Icatu were evaluated. Plants were grown at 380 or 700 μL CO 2 L -1 air, and then submitted to a gradual temperature rise from 25°C up to 40°C during ca. 4 months. Fruits were harvested at 25°C, and in the ranges of 30-35 or 36-40°C, and bean physical and chemical attributes with potential implications on quality were then examined. These included: color, phenolic content, soluble solids, chlorogenic, caffeic and p -coumaric acids, caffeine, trigonelline, lipids, and minerals. Most of these parameters were mainly affected by temperature (although without a strong negative impact on bean quality), and only marginally, if at all, by elevated [CO 2 ]. However, the [CO 2 ] vs. temperature interaction strongly attenuated some of the negative impacts promoted by heat (e.g., total chlorogenic acids), thus maintaining the bean characteristics closer to those obtained under adequate temperature conditions (e.g., soluble solids, caffeic and p -coumaric acids, trigonelline, chroma, Hue angle, and color index), and increasing desirable features (acidity). Fatty acid and mineral pools remained quite stable, with only few modifications due to elevated air [CO 2 ] (e.g., phosphorous) and/or heat. In conclusion, exposure to high temperature in the last stages of fruit maturation did not strongly depreciate bean quality, under the conditions of unrestricted water supply and moderate irradiance. Furthermore, the superimposition of elevated air [CO 2 ] contributed to preserve bean quality by modifying and mitigating

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

How We Got to the Northern Hemisphere Ice Ages: Late Miocene Global Cooling and Plate Tectonic CO2 Forcing

Science.gov (United States)

Herbert, T.; Dalton, C. A.; Carchedi, C.

2017-12-01

The evolution of Earth's climate between "refrigeration" of East Antarctica and the onset of cyclic Northern Hemisphere glaciation spanned more than 11 Myr. In the latest Miocene (Messinian) time, approximately half way on this journey, changes on land, ranging from the expansion of arid zones to major floral and faunal ecosystem shifts, accelerated. Recent compilations of marine surface temperatures reveal that global cooling from the Miocene Optimum (14-16Ma) also accelerated in late Miocene (7-5.35 Ma) time to reach temperatures not much above Holocene conditions. Both hemispheres cooled in parallel, with the changes amplified at higher latitudes in comparison to the tropics. Despite the strong circumstantial case for CO2 decline as the dominant cause of late Miocene climatic and evolutionary change, proxy indicators of CO2concentrations paint an equivocal picture of greenhouse forcing. Here we provide evidence that global sea floor spreading (SFS) rates decelerated at exactly the times of major climatic cooling, linking a decline in tectonic degassing (at both subduction zones and mid-ocean ridges) to fundamental shifts in the global carbon cycle. Our work utilizes newly available global compilations of seafloor fabric and marine magnetic anomalies provided by the NSF-funded Global Seafloor Fabric and Magnetic Lineation Data Base Project. Previous global compilations of SFS typically binned estimates over 10 Myr increments, losing critical resolution on the timescale of late Neogene climate changes. We further improve the signal:noise of SFS estimates by incorporating recent advances in the astronomical calibration of the Miocene geomagnetic polarity timescale. We use two approaches to compile spreading rate estimates over the past 20 Myr at each spreading system: optimized finite rotation calculations, and averages of sea floor-spreading derived from the distances of magnetic lineations along flow lines on the sea floor. Weighted by ridge length, we find an 25

Global High Resolution Sea Surface Flux Parameters From Multiple Satellites

Science.gov (United States)

Zhang, H.; Reynolds, R. W.; Shi, L.; Bates, J. J.

2007-05-01

Advances in understanding the coupled air-sea system and modeling of the ocean and atmosphere demand increasingly higher resolution data, such as air-sea fluxes of up to 3 hourly and every 50 km. These observational requirements can only be met by utilizing multiple satellite observations. Generation of such high resolution products from multiple-satellite and in-situ observations on an operational basis has been started at the U.S. National Oceanic and Atmospheric Administration (NOAA) National Climatic Data Center. Here we describe a few products that are directly related to the computation of turbulent air-sea fluxes. Sea surface wind speed has been observed from in-situ instruments and multiple satellites, with long-term observations ranging from one satellite in the mid 1987 to six or more satellites since mid 2002. A blended product with a global 0.25° grid and four snapshots per day has been produced for July 1987 to present, using a near Gaussian 3-D (x, y, t) interpolation to minimize aliases. Wind direction has been observed from fewer satellites, thus for the blended high resolution vector winds and wind stresses, the directions are taken from the NCEP Re-analysis 2 (operationally run near real time) for climate consistency. The widely used Reynolds Optimum Interpolation SST analysis has been improved with higher resolutions (daily and 0.25°). The improvements use both infrared and microwave satellite data that are bias-corrected by in- situ observations for the period 1985 to present. The new versions provide very significant improvements in terms of resolving ocean features such as the meandering of the Gulf Stream, the Aghulas Current, the equatorial jets and other fronts. The Ta and Qa retrievals are based on measurements from the AMSU sounder onboard the NOAA satellites. Ta retrieval uses AMSU-A data, while Qa retrieval uses both AMSU-A and AMSU-B observations. The retrieval algorithms are developed using the neural network approach. Training

Air pollution, greenhouse gases and climate change: Global and regional perspectives

Science.gov (United States)

Ramanathan, V.; Feng, Y.

Greenhouse gases (GHGs) warm the surface and the atmosphere with significant implications for rainfall, retreat of glaciers and sea ice, sea level, among other factors. About 30 years ago, it was recognized that the increase in tropospheric ozone from air pollution (NO x, CO and others) is an important greenhouse forcing term. In addition, the recognition of chlorofluorocarbons (CFCs) on stratospheric ozone and its climate effects linked chemistry and climate strongly. What is less recognized, however, is a comparably major global problem dealing with air pollution. Until about ten years ago, air pollution was thought to be just an urban or a local problem. But new data have revealed that air pollution is transported across continents and ocean basins due to fast long-range transport, resulting in trans-oceanic and trans-continental plumes of atmospheric brown clouds (ABCs) containing sub micron size particles, i.e., aerosols. ABCs intercept sunlight by absorbing as well as reflecting it, both of which lead to a large surface dimming. The dimming effect is enhanced further because aerosols may nucleate more cloud droplets, which makes the clouds reflect more solar radiation. The dimming has a surface cooling effect and decreases evaporation of moisture from the surface, thus slows down the hydrological cycle. On the other hand, absorption of solar radiation by black carbon and some organics increase atmospheric heating and tend to amplify greenhouse warming of the atmosphere. ABCs are concentrated in regional and mega-city hot spots. Long-range transport from these hot spots causes widespread plumes over the adjacent oceans. Such a pattern of regionally concentrated surface dimming and atmospheric solar heating, accompanied by widespread dimming over the oceans, gives rise to large regional effects. Only during the last decade, we have begun to comprehend the surprisingly large regional impacts. In S. Asia and N. Africa, the large north-south gradient in the ABC

Fixation of CO2 in air: Synthesis and crystal structure of a µ3-CO3 ...

Indian Academy of Sciences (India)

Unknown

Fixation of CO2 in air: Synthesis and crystal structure of a ... from the reaction between copper(I) complexes and dioxygen.2,6,7 ... and co-workers from the reaction of [(L2) ..... followed by water dissociation.13h,24 While fixation of CO2 by ...

Rapid establishment of the CO2 sink associated with Kerguelen's bloom observed during the KEOPS2/OISO20 cruise

Science.gov (United States)

Lo Monaco, C.; Metzl, N.; D'Ovidio, F.; Llort, J.; Ridame, C.

2014-12-01

Iron and light are the main factors limiting the biological pump of CO2 in the Southern Ocean. Iron fertilization experiments have demonstrated the potential for increased uptake of atmospheric CO2, but little is known about the evolution of fertilized environnements. This paper presents observations collected in one of the largest phytoplankton bloom of the Southern Ocean sustained by iron originating from the Kerguelen Plateau. We first complement previous studies by investigating the mechanisms that control air-sea CO2 fluxes over and downstream of the Kerguelen Plateau at the onset of the bloom based on measurements obtained in October-November 2011. These new observations show the rapid establishment of a strong CO2 sink in waters fertilized with iron as soon as vertical mixing is reduced. The magnitude of the CO2 sink was closely related to chlorophyll a and iron concentrations. Because iron concentration strongly depends on the distance from the iron source and the mode of delivery, we identified lateral advection as the main mechanism controlling air-sea CO2 fluxes downtream the Kerguelen Plateau during the growing season. In the southern part of the bloom, situated over the Plateau (iron source), the CO2 sink was stronger and spatially more homogeneous than in the plume offshore. However, we also witnessed a substantial reduction in the uptake of atmospheric CO2 over the Plateau following a strong winds event. Next, we used all the data available in this region in order to draw the seasonal evolution of air-sea CO2 fluxes. The CO2 sink is rapidly reduced during the course of the growing season, which we attribute to iron and silicic acid depletion. South of the Polar Front, where nutrients depletion is delayed, we suggest that the amplitude and duration of the CO2 sink is mainly controlled by vertical mixing. The impact of iron fertilization on air-sea CO2 fluxes is revealed by comparing the uptake of CO2 integrated over the productive season in the bloom

Application of vertical advection-diffusion model for studying CO2 and O2 profiles in central Arabian Sea

Digital Repository Service at National Institute of Oceanography (India)

AnilKumar, N.; Singbal, S.Y.S.

The vertical advection-diffusion model proposed by Craig has been applied to the study of CO sub(2) and O sub(2) profiles in Central Arabian Sea. Distributions of total CO Sub(2) and O sub(2) are explained better by expressions involving exponential...

Using Argo-O2 data to examine the impact of deep-water formation events on oxygen uptake in the Labrador Sea

Science.gov (United States)

Wolf, M. K.; Hamme, R. C.; Gilbert, D.; Yashayaev, I.

2016-02-01

Deep-water formation allows the deep ocean to communicate with the atmosphere, facilitating exchanges of heat as well as important gases such as CO2 and oxygen. The Labrador Sea is the most studied location of deep convection in the North Atlantic Ocean and a strong contributor to the global thermohaline circulation. Since there are no internal sources of oxygen below the euphotic zone, deep-water formation is vital for oxygen transport to the deep ocean. Recent studies document large interannual variability in the strength and depth of convection in the Labrador Sea, from mixed layers of 100m to greater than 1000m. A weakening of this deep convection starves the deep ocean of oxygen, disrupting crucial deep sea biological processes, as well as reducing oceanic CO2 uptake and ocean circulation. We used data from the extensive Argo float network to examine these deep-water formation events in the Labrador Sea. The oxygen optodes onboard many Argo floats suffer from biases whose amplitude must be determined; therefore we investigated and applied various optode calibration methods. Using calibrated vertical profiles of oxygen, temperature, and salinity, we observed the timing, magnitude, and location of deep convection, restratification, and spring phytoplankton blooms. In addition, we used surface oxygen values along with NCEP wind speeds to calculate the air-sea oxygen flux using a range of air-sea gas exchange parameterizations. We then compared this oxygen flux to the rate of change of the measured oxygen inventory. Where the inventory and flux did not agree, we identified other oceanic processes such as biological activity or lateral advection of water masses occurring, or advection of the float itself into a new area. The large role that horizontal advection of water or the float has on oxygen uptake and cycling leads us to conclude that this data cannot be easily interpreted as a 1-D system. Oxygen exchanges with the atmosphere at a faster rate than CO2, is

A global CO2 tax for sustainable development?

DEFF Research Database (Denmark)

Brandt, Urs Steiner; Svendsen, Gert Tinggaard

2014-01-01

The Rio+20 conference in 2012 called for goals of promoting green industries and improving the quality of institutions worldwide. Is a global CO2 tax the best global solution for achieving this twin goal? As most countries in the world are highly corrupt, an adequate regulatory instrument should...... and sustainability conferences substantially since the focus is on one issue rather than many....

The economics of CO2-EOR cluster developments in the UK Central North Sea

International Nuclear Information System (INIS)

Kemp, Alexander G.; Kasim, Sola

2013-01-01

Studies to date have generally shown that individual CO 2 -EOR offshore projects are uneconomic except under questionable assumptions. The present study is based on an interconnected cluster of nine oilfields in the Central North Sea linked to an onshore CO 2 collection hub by a set of existing and new pipelines. Monte Carlo simulation modelling was undertaken of the prospective returns to investments in CO 2 -EOR in the fields. Relatively high oil prices were employed for the study period (2020–2050) and two contrasting CO 2 transfer price scenarios, the first being the Carbon Price Floor (CPF) introduced by the UK Government and the second being relatively low negotiated prices reflecting recent and prospective levels under the EU-ETS. At CPF prices the investment returns were all found to be negative, but at prices averaging £10 per tonne positive returns were generally achieved. The study emphasises the importance of CO 2 prices and the taxation system in determining the viability of the investments. - Highlights: • Detailed modelling of CO 2 EOR in nine North Sea oil fields. • Overall investment risks are demonstrated to be very high. • Sharing of pipelines in network and cluster of CO 2 -EOR fields significantly reduces investment costs. • Range of plausible CO 2 prices paid by investor results in very wide range of returns from CO 2 -EOR. • CO 2 pricing and tax arrangements for EOR need further attention by policy makers

Assessing the influence of regional transport from Mainland China over the Korean Peninsula during the 2016 KORUS-AQ Field Campaign with CO/CO2 ratios

Science.gov (United States)

Halliday, H. S.; DiGangi, J. P.; Diskin, G. S.; Choi, Y.; Pusede, S.; Rana, M.; Nowak, J. B.

2017-12-01

The industrial growth in East Asia has resulted in widespread growth and prosperity, but has been accompanied by degraded air quality. These poor air quality events have both local and regional effects, and long range transportation of pollution can greatly increase the affected populations. South Korea has a technologically oriented economy with vibrant urban regions, but suffers from poor air quality arising from both local emissions on the Korean peninsula and from the transport of pollution from Mainland China. The KORUS-AQ field campaign was an international collaboration to characterize and understand the air quality over the Korean peninsula in the spring of 2016. We use the aircraft in situ data from the DC-8 aircraft to examine trace gas ratios over three major analysis regions: the Seoul Metropolitan region, the South Korean peninsula, and the West Sea (Yellow Sea). We look specifically at the correlations between CO and CO2 as an indicator of emissions type, with low ratios generally indicative of more efficient combustion and high emission ratios indicating low efficiency combustion. At low altitudes, higher incidences of low CO/CO2 ratios were observed in the Seoul and Peninsula regions, compared to higher ratios of CO/CO2 over the West Sea. We examine the meteorological dependence of these carbon species ratios, their relationships to VOC tracers, and their vertical behavior to evaluate the air mass contributions from Mainland China and assess the percentage contributions of these regional emissions to the measurements over the Korean Peninsula.

A system for high-quality CO2 isotope analyses of air samples collected by the CARIBIC Airbus A340-600.

Science.gov (United States)

Assonov, S; Taylor, P; Brenninkmeijer, C A M

2009-05-01

delta18O(CO2) on the VPDB-CO2 scale, estimated on runs of CO2-air mixtures, is +/-0.040 per thousand and 0.060 per thousand (2-sigma values). Inter-comparison with MPI-BGC resulted in a scale discrepancy of a similar magnitude. Although the reason(s) for this discrepancy still need to be understood, this basically confirms the approach of using specifically prepared CO2-air mixtures as a calibration carrier, in order to achieve scale unification among laboratories. As important practical application and as a critical test, JRC-IRMM took part in the passenger aircraft-based global monitoring project CARIBIC (http://www.caribic-atmospheric.com). In this way, reliable CO2 isotope data for the tropopause region and the free troposphere were obtained. From June 2007 to January 2009, approximately 500 CARIBIC air samples have been analysed. Some flights demonstrated a compact correlation of both delta13C(CO2) and delta18O(CO2) with respect to CO2 concentration, demonstrating mixing of tropospheric and stratospheric air masses. These excellent correlations provide an independent, realistic data quality check. Copyright (c) 2009 John Wiley & Sons, Ltd.

Dynamics of sea-ice biogeochemistry in the coastal Antarctica during transition from summer to winter

Directory of Open Access Journals (Sweden)

Suhas Shetye

2017-05-01

Full Text Available The seasonality of carbon dioxide partial pressure (pCO2, air-sea CO2 fluxes and associated environmental parameters were investigated in the Antarctic coastal waters. The in-situ survey was carried out from the austral summer till the onset of winter (January 2012, February 2010 and March 2009 in the Enderby Basin. Rapid decrease in pCO2 was evident under the sea-ice cover in January, when both water column and sea-ice algal activity resulted in the removal of nutrients and dissolved inorganic carbon (DIC and increase in pH. The major highlight of this study is the shift in the dominant biogeochemical factors from summer to early winter. Nutrient limitation (low Si/N, sea-ice cover, low photosynthetically active radiation (PAR, deep mixed layer and high upwelling velocity contributed towards higher pCO2 during March (early winter. CO2 fluxes suggest that the Enderby Basin acts as a strong CO2 sink during January (−81 mmol m−2 d−1, however it acts as a weak sink of CO2 with −2.4 and −1.7 mmol m−2 d−1 during February and March, respectively. The present work, concludes that sea ice plays a dual role towards climate change, by decreasing sea surface pCO2 in summer and enhancing in early winter. Our observations emphasize the need to address seasonal sea-ice driven CO2 flux dynamics in assessing Antarctic contributions to the global oceanic CO2 budget.

AIRS/Aqua Level 3 Monthly CO2 in the free troposphere (AIRS-only) V005

Data.gov (United States)

National Aeronautics and Space Administration — This is the AIRS mid-tropospheric Carbon Dioxide (CO2) Level 3 Monthly Gridded Retrieval, from the AIRS instrument on board of Aqua satellite. It is a monthly...

Wintertime Air-Sea Gas Transfer Rates and Air Injection Fluxes at Station Papa in the NE Pacific

Science.gov (United States)

McNeil, C.; Steiner, N.; Vagle, S.

2008-12-01

In recent studies of air-sea fluxes of N2 and O2 in hurricanes, McNeil and D'Asaro (2007) used a simplified model formulation of air-sea gas flux to estimate simultaneous values of gas transfer rate, KT, and air injection flux, VT. The model assumes air-sea gas fluxes at high to extreme wind speeds can be explained by a combination of two processes: 1) air injection, by complete dissolution of small bubbles drawn down into the ocean boundary layer by turbulent currents, and 2) near-surface equilibration processes, such as occurs within whitecaps. This analysis technique relies on air-sea gas flux estimates for two gases, N2 and O2, to solve for the two model parameters, KT and VT. We present preliminary results of similar analysis of time series data collected during winter storms at Station Papa in the NE Pacific during 2003/2004. The data show a clear increase in KT and VT with increasing NCEP derived wind speeds and acoustically measured bubble penetration depth.

First assessment on the air CO2 dynamic in the show caves of tropical karst, Vietnam

Directory of Open Access Journals (Sweden)

Duc A. Trinh

2018-01-01

Full Text Available In this study, air, water, and host rock in show caves in a Vietnam’s karst region was monitored and analyzed to identify the ventilation regime and track the cave air CO2 sources. In general, the studied caves are well ventilated. In dynamic – multiple entrance caves, air ventilation is described with the use of U shape model. In static – single entrance cave, air circulation is explained by cold air trap model. Both ventilation models suggest that air is more circulated in winter than in summer. Seasonally, the cave air CO2 increases from early spring to summer. Value in the deepest part of the single-entrance cave is approximately 1,000 ppmv and 8,000 ppmv in early spring and summer, respectively. In multiple-entrance and wet caves, CO2 level is fairly constant all over the show section, increasing from 500 ppmv in early spring to 2,000 ppmv in summer. Data of microclimate, CO2 content, and particularly δ13C show that cave air, particularly in single entrance cave, has higher CO2 concentration during summer due to a stagnation of cave air circulation and an elevated CO2 input from soil and epikarst. The cave air CO2 increase is also observed after intense rainfalls. A factor that increase cave air CO2 in show caves during the festive days could probably be huma n exhaling but the extent of human factor in these studied cave systems should be further investigated. Cave waters including cave pools and streams mediate CO2 level in wet caves. Above all, the atmospheric fraction of CO2 is always dominant (>60% in all cave sections.

Implications of overestimated anthropogenic CO2 emissions on East Asian and global land CO2 flux inversion

Science.gov (United States)

Saeki, Tazu; Patra, Prabir K.

2017-12-01

Measurement and modelling of regional or country-level carbon dioxide (CO2) fluxes are becoming critical for verification of the greenhouse gases emission control. One of the commonly adopted approaches is inverse modelling, where CO2 fluxes (emission: positive flux, sink: negative flux) from the terrestrial ecosystems are estimated by combining atmospheric CO2 measurements with atmospheric transport models. The inverse models assume anthropogenic emissions are known, and thus the uncertainties in the emissions introduce systematic bias in estimation of the terrestrial (residual) fluxes by inverse modelling. Here we show that the CO2 sink increase, estimated by the inverse model, over East Asia (China, Japan, Korea and Mongolia), by about 0.26 PgC year-1 (1 Pg = 1012 g) during 2001-2010, is likely to be an artifact of the anthropogenic CO2 emissions increasing too quickly in China by 1.41 PgC year-1. Independent results from methane (CH4) inversion suggested about 41% lower rate of East Asian CH4 emission increase during 2002-2012. We apply a scaling factor of 0.59, based on CH4 inversion, to the rate of anthropogenic CO2 emission increase since the anthropogenic emissions of both CO2 and CH4 increase linearly in the emission inventory. We find no systematic increase in land CO2 uptake over East Asia during 1993-2010 or 2000-2009 when scaled anthropogenic CO2 emissions are used, and that there is a need of higher emission increase rate for 2010-2012 compared to those calculated by the inventory methods. High bias in anthropogenic CO2 emissions leads to stronger land sinks in global land-ocean flux partitioning in our inverse model. The corrected anthropogenic CO2 emissions also produce measurable reductions in the rate of global land CO2 sink increase post-2002, leading to a better agreement with the terrestrial biospheric model simulations that include CO2-fertilization and climate effects.

Response of air-sea carbon fluxes and climate to orbital forcing changes in the Community Climate System Model

Science.gov (United States)

Jochum, M.; Peacock, S.; Moore, K.; Lindsay, K.

2010-07-01

A global general circulation model coupled to an ocean ecosystem model is used to quantify the response of carbon fluxes and climate to changes in orbital forcing. Compared to the present-day simulation, the simulation with the Earth's orbital parameters from 115,000 years ago features significantly cooler northern high latitudes but only moderately cooler southern high latitudes. This asymmetry is explained by a 30% reduction of the strength of the Atlantic Meridional Overturning Circulation that is caused by an increased Arctic sea ice export and a resulting freshening of the North Atlantic. The strong northern high-latitude cooling and the direct insolation induced tropical warming lead to global shifts in precipitation and winds to the order of 10%-20%. These climate shifts lead to regional differences in air-sea carbon fluxes of the same order. However, the differences in global net air-sea carbon fluxes are small, which is due to several effects, two of which stand out: first, colder sea surface temperature leads to a more effective solubility pump but also to increased sea ice concentration which blocks air-sea exchange, and second, the weakening of Southern Ocean winds that is predicted by some idealized studies occurs only in part of the basin, and is compensated by stronger winds in other parts.

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.)

AIRS/Aqua Level 3 Monthly CO2 in the free troposphere (AIRS+AMSU) V005

Data.gov (United States)

National Aeronautics and Space Administration — This is the AIRS mid-tropospheric Carbon Dioxide (CO2) Level 3 Monthly Gridded Retrieval, from the AIRS and AMSU instruments on board of Aqua satellite. It is a...

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

Directory of Open Access Journals (Sweden)

A. Roobaert

2018-03-01

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

Processes regulating pCO2 in the surface waters of the central eastern Gotland Sea: a model study

Directory of Open Access Journals (Sweden)

Bernd Schneider

2011-09-01

Full Text Available This work presents a one-dimensional simulation of the seasonal changes in CO2 partial pressure (pCO2. The results of the model were constrained using data from observations, which improved the model's ability to estimate nitrogen fixation in the central Baltic Sea and allowed the impact of nitrogen fixation on the ecological state of the Baltic Sea to be studied. The model used here is the public domain water-column model GOTM (General Ocean Turbulence Model, which in this study was coupled with a modifed Baltic Sea ecosystem model, ERGOM (The Baltic Sea Research Institute's ecosystem model. To estimate nitrogen fixation rates in the Gotland Sea, the ERGOM model was modified by including an additional cyanobacteria group able to fix nitrogen from March to June. Furthermore, the model was extended by a simple CO2 cycle. Variable C:P and N:P ratios, controlled by phosphate concentrations in ambient water, were used to represent cyanobacteria, detritus and sediment detritus. This approach improved the model's ability to reproduce sea-surface phosphate and pCO2 dynamics. The resulting nitrogen fixation rates in 2005 for the two simulations, with and without the additional cyanobacteria group, were 259 and 278 mmol N m-2 year-1respectively.

Air-sea exchange of gaseous mercury in the tropical coast (Luhuitou fringing reef) of the South China Sea, the Hainan Island, China.

Science.gov (United States)

Ci, Zhijia; Zhang, Xiaoshan; Wang, Zhangwei

2016-06-01

The air-sea exchange of gaseous mercury (mainly Hg(0)) in the tropical ocean is an important part of the global Hg biogeochemical cycle, but the related investigations are limited. In this study, we simultaneously measured Hg(0) concentrations in surface waters and overlaying air in the tropical coast (Luhuitou fringing reef) of the South China Sea (SCS), Hainan Island, China, for 13 days on January-February 2015. The purpose of this study was to explore the temporal variation of Hg(0) concentrations in air and surface waters, estimate the air-sea Hg(0) flux, and reveal their influencing factors in the tropical coastal environment. The mean concentrations (±SD) of Hg(0) in air and total Hg (THg) in waters were 2.34 ± 0.26 ng m(-3) and 1.40 ± 0.48 ng L(-1), respectively. Both Hg(0) concentrations in waters (53.7 ± 18.8 pg L(-1)) and Hg(0)/THg ratios (3.8 %) in this study were significantly higher than those of the open water of the SCS in winter. Hg(0) in waters usually exhibited a clear diurnal variation with increased concentrations in daytime and decreased concentrations in nighttime, especially in cloudless days with low wind speed. Linear regression analysis suggested that Hg(0) concentrations in waters were positively and significantly correlated to the photosynthetically active radiation (PAR) (R (2) = 0.42, p sea Hg(0) fluxes were estimated to be 1.73 ± 1.25 ng m(-2) h(-1) with a large range between 0.01 and 6.06 ng m(-2) h(-1). The high variation of Hg(0) fluxes was mainly attributed to the greatly temporal variation of wind speed.

CO2 enhanced oil recovery and storage in the North Sea - a UK perspective

International Nuclear Information System (INIS)

Beckly, Andy; Hughes, David S.

2006-01-01

Considerable technical and economic challenges must be overcome if the potential for CO 2 injection and sequestration is to be fully realised. However, there is an opportunity to exploit the synergy between the need to reduce CO 2 emissions and the potential to use CO 2 to increase North Sea oil reserves and extend the life of the basin. This opportunity is available now, while the infrastructure remains in place

The Idea of Global CO2 Trade

DEFF Research Database (Denmark)

Svendsen, Gert Tinggaard

1998-01-01

-effective control which can solve future global environmental problems. The gains from CO2 trade may give vital financial subsidies from the EU to Eastern Europe, for example, and it will probably not pay to cheat if quotas are renewed periodically by the UN. Cheating countries are then to be excluded from further...

Global Cooling: Policies to Cool the World and Offset Global Warming from CO2 Using Reflective Roofs and Pavements

Energy Technology Data Exchange (ETDEWEB)

Akbari, Hashem; Levinson, Ronnen; Rosenfeld, Arthur; Elliot, Matthew

2009-08-28

Increasing the solar reflectance of the urban surface reduce its solar heat gain, lowers its temperatures, and decreases its outflow of thermal infrared radiation into the atmosphere. This process of 'negative radiative forcing' can help counter the effects of global warming. In addition, cool roofs reduce cooling-energy use in air conditioned buildings and increase comfort in unconditioned buildings; and cool roofs and cool pavements mitigate summer urban heat islands, improving outdoor air quality and comfort. Installing cool roofs and cool pavements in cities worldwide is a compelling win-win-win activity that can be undertaken immediately, outside of international negotiations to cap CO{sub 2} emissions. We propose an international campaign to use solar reflective materials when roofs and pavements are built or resurfaced in temperate and tropical regions.

Ikaite crystals in melting sea ice – implications for pCO2 and pH levels in Arctic surface waters

Directory of Open Access Journals (Sweden)

R. J. G. Leakey

2012-08-01

Full Text Available A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air–sea CO2 exchange. This has been complicated by the recent discoveries of ikaite (a polymorph of CaCO3·6H2O in Arctic and Antarctic sea ice, which indicate that multiple chemical transformations occur in sea ice with a possible effect on CO2 and pH conditions in surface waters. Here, we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from a melting 1.7 km2 (0.5–1 m thick drifting ice floe in the Fram Strait during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice floe thickness by 0.2 m per week and resulted in an estimated 3.8 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air–sea CO2 uptake of 10.6 mmol m−2 sea ice d−1 or to 3.3 ton km−2 ice floe week−1. This is markedly higher than the estimated primary production within the ice floe of 0.3–1.3 mmol m−2 sea ice d−1. Finally, the presence of ikaite in sea ice and the dissolution of the mineral during melting of the sea ice and mixing of the melt water into the surface oceanic mixed layer accounted for half of the estimated pCO2 uptake.

Children's exposure to indoor air in urban nurseries-part I: CO2 and comfort assessment

International Nuclear Information System (INIS)

Branco, P.T.B.S.; Alvim-Ferraz, M.C.M.; Martins, F.G.; Sousa, S.I.V.

2015-01-01

Indoor air quality (IAQ) in nurseries is an emerging case-study. Thus, this study, as the Part I of the larger study “Children's exposure to indoor air in urban nurseries”, aimed to: i) evaluate nurseries’ indoor concentrations of carbon dioxide (CO 2 ), a global IAQ indicator, in class and lunch rooms; ii) assess indoor comfort parameters–temperature (T) and relative humidity (RH); and iii) analyse them according to guidelines and references for IAQ, comfort and children's health. Indoor continuous measurements were performed. Non-compliances with guidelines were found in comfort parameters, which could cause discomfort situations and also microbial proliferation. Exceedances in CO 2 concentrations were also found and they were caused by poor ventilation and high classroom occupation. More efficient ventilation and control of comfort parameters, as well as to reduce occupation by reviewing Portuguese legislation on that matter, would certainly improve IAQ and comfort in nurseries and consequently safeguard children's health. - Highlights: • High occupation and poor ventilation were main determinants of IAQ in nurseries. • T and RH indoor values found in nurseries are likely to cause thermal discomfort. • Building characteristics and an inadequate ventilation determined T and RH values. • High CO 2 concentrations found could indicate accumulation of other air pollutants

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.

Air Pollution, Global Change and Forests in the New Millennium

International Nuclear Information System (INIS)

Karnosky, D.F.; Pikkarainen, J.; Percy, K.E.; Simpson, C.; Chappelka, A.H.

2003-01-01

The chapters in this book present a snapshot of the state of knowledge of air pollution effects at the beginning of the 21st century. From their different disciplines, a distinguished collection of authors document their understanding of how leaves, trees, and forests respond to air pollutants and climate change. Scenarios of global change and air pollution are described. The authors describe responses of forests to climate variability, tropospheric ozone, rising atmospheric CO2, the combination of CO2 and ozone, and deposition of acidic compounds and heavy metals. The responses to ozone receive particular attention because of increasing concern about its damaging effects and increasing concentrations in rural areas. Scaling issues are addressed - from leaves to trees, from juvenile trees to mature trees, from short-term responses to long-term responses, and from small-scale experiments and observations to large-scale forest ecosystems. This book is one major product of a conference sponsored by the International Union of Forestry Research Organizations, the USDA Forest Service Global Change Northern Stations Program, the Arthur Ross Foundation, NCASI, the Canadian Forest Service, and Michigan Technological University. The conference was held in May 2000 in Houghton, Michigan, USA

Stem respiration of Populus species in the third year of free-air CO2 enrichment.

Science.gov (United States)

Gielen, Birgit; Scarascia-Mugnozza, Giuseppe; Ceulemans, Reinhart

2003-04-01

Carbon cycling in ecosystems, and especially in forests, is intensively studied to predict the effects of global climate change, and the role which forests may play in 'changing climate change'. One of the questions is whether the carbon balance of forests will be affected by increasing atmospheric CO2 concentrations. Regarding this question, effects of elevated [CO2] on woody-tissue respiration have frequently been neglected. Stem respiration of three Populus species (P. alba L. (Clone 2AS-11), P. nigra L. (Clone Jean Pourtet), and P. x euramericana (Clone I-214)) was measured in a managed, high-density forest plantation exposed to free-air CO2 enrichment (POPFACE). During the period of measurements, in May of the third year, stem respiration rates were not affected by the FACE treatment. Moreover, FACE did not influence the relationships between respiration rate and both stem temperature and relative growth rate. The results were supported by the reported absence of a FACE-effect on growth and stem wood density.

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

Estimating surface CO2 fluxes from space-borne CO2 dry air mole fraction observations using an ensemble Kalman Filter

Directory of Open Access Journals (Sweden)

S. Dance

2009-04-01

Full Text Available We have developed an ensemble Kalman Filter (EnKF to estimate 8-day regional surface fluxes of CO2 from space-borne CO2 dry-air mole fraction observations (XCO2 and evaluate the approach using a series of synthetic experiments, in preparation for data from the NASA Orbiting Carbon Observatory (OCO. The 32-day duty cycle of OCO alternates every 16 days between nadir and glint measurements of backscattered solar radiation at short-wave infrared wavelengths. The EnKF uses an ensemble of states to represent the error covariances to estimate 8-day CO2 surface fluxes over 144 geographical regions. We use a 12×8-day lag window, recognising that XCO2 measurements include surface flux information from prior time windows. The observation operator that relates surface CO2 fluxes to atmospheric distributions of XCO2 includes: a the GEOS-Chem transport model that relates surface fluxes to global 3-D distributions of CO2 concentrations, which are sampled at the time and location of OCO measurements that are cloud-free and have aerosol optical depths 2 profiles to XCO2, accounting for differences between nadir and glint measurements, and the associated scene-dependent observation errors. We show that OCO XCO2 measurements significantly reduce the uncertainties of surface CO2 flux estimates. Glint measurements are generally better at constraining ocean CO2 flux estimates. Nadir XCO2 measurements over the terrestrial tropics are sparse throughout the year because of either clouds or smoke. Glint measurements provide the most effective constraint for estimating tropical terrestrial CO2 fluxes by accurately sampling fresh continental outflow over neighbouring oceans. We also present results from sensitivity experiments that investigate how flux estimates change with 1 bias and unbiased errors, 2 alternative duty cycles, 3 measurement density and correlations, 4 the spatial resolution of estimated flux estimates, and 5 reducing the length of the lag window and the

Deep oceans may acidify faster than anticipated due to global warming

Science.gov (United States)

Chen, Chen-Tung Arthur; Lui, Hon-Kit; Hsieh, Chia-Han; Yanagi, Tetsuo; Kosugi, Naohiro; Ishii, Masao; Gong, Gwo-Ching

2017-12-01

Oceans worldwide are undergoing acidification due to the penetration of anthropogenic CO2 from the atmosphere1-4. The rate of acidification generally diminishes with increasing depth. Yet, slowing down of the thermohaline circulation due to global warming could reduce the pH in the deep oceans, as more organic material would decompose with a longer residence time. To elucidate this process, a time-series study at a climatically sensitive region with sufficient duration and resolution is needed. Here we show that deep waters in the Sea of Japan are undergoing reduced ventilation, reducing the pH of seawater. As a result, the acidification rate near the bottom of the Sea of Japan is 27% higher than the rate at the surface, which is the same as that predicted assuming an air-sea CO2 equilibrium. This reduced ventilation may be due to global warming and, as an oceanic microcosm with its own deep- and bottom-water formations, the Sea of Japan provides an insight into how future warming might alter the deep-ocean acidification.

Carbon Dioxide Impacts in the Deep-Sea: Is Maintaining a Metabolically Required CO2 Efflux Rate Challenging?

Science.gov (United States)

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

2011-12-01

Increasing ocean acidification from fossil fuel CO2 invasion, from temperature driven changes in respiration, and from possible leakage from sub-seabed geologic CO2 disposal has aroused concern over the impacts of elevated CO2 concentrations on marine life. Here we describe the rate problem for animals who must export CO2 at about the same rate at which O2 is consumed. We analyze the basic properties controlling CO2 export within the diffusive boundary of marine animals in a changing ocean in order to compare the challenges posed by O2 uptake under stress with the equivalent problem of CO2 expulsion. The problem is more complex than that for a non-reactive gas since, as with gas exchange of CO2 at the air-sea interface, the influence of the ensemble of reactions within the CO2 - HCO3- - CO3= acid-base system needs to be considered. These reactions appear as an enhancement factor which significantly facilitates CO2 efflux compared to O2 intake at equal temperature, pressure and flow rate under typical oceanic concentrations. Possibly as an adaptation to this chemical advantage marine animals typically can respond to external CO2 stress simply by metabolic adjustment. This is energetically more favorable than having to resort to mechanically increasing flow over their surface to thin the boundary layer as is required to alleviate O2 stress. Regionally as with O2 the combination of T, P, and pH/pCO2 creates a zone of maximum CO2 stress at around 1000 m depth. But the net result is that the combination of an increase in T combined with declining O2 poses a greater respiratory challenge to marine life than does increasing CO2. The relationships developed here allow a more accurate prediction of the impacts on marine life from the combined effects of changing T, O2, and CO2 than can be estimated from single variable studies.

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

Evaluation of co-benefits from combined climate change and air pollution reduction strategies

Science.gov (United States)

Leitao, Joana; Van Dingenen, Rita; Dentener, Frank; Rao, Shilpa

2014-05-01

The connection of climate change and air pollution is becoming more relevant in the process of policy making and implementation of emission control strategies because of resulting co-benefits and trade-offs. Some sectors, such as fossil fuel combustion, are sources of both pollutants (NOx and PM) as well as greenhouse gas (CO2). Additionally, the use of wood burning as biofuel to reduce climate impact may in fact deteriorate air quality. Furthermore, several air pollutants are important radiative forcers and regulating their emissions impacts on climate. It is evident that both problems need to be undertaken with a common strategy and the existence of cross-policy with co-benefits may encourage their implementation. The LIMITS FP7 project (http://www.feem-project.net/limits/index.html) was designed with the main goal of assessing strategies for reduction of GHG emissions so that the 2°C target can be achieved. The work developed focus on the evaluation of the implementation of strategies analysing several aspects of different scenarios, namely: the feasibility of low carbon scenarios in terms of available technologies and infrastructure, the required financial mechanisms, and also the co-benefits regarding energy security, economic development and air pollution. For the latter, five integrated assessment models (IAMs) provided greenhouse gases and pollutant emission values for several scenarios. These were based on air pollution scenarios defined according to stringency and implementation of future global legislation. They which were also combined with 2 climate policy scenarios (no climate policy and 2.8 W/m2 target). The former are mostly focused on non-climate policies and technical control measures for emissions of air pollutants, such as PM2.5, NOx and SO2, with their emission factors harmonized between the IAMs. With the global air quality source-receptor model TM5-FASST the impact of the resulting emissions was analysed and the co-benefits of combined

Does air-sea coupling influence model projections of the effects of the Paris Agreement?

Science.gov (United States)

Klingaman, Nicholas; Suckling, Emma; Sutton, Rowan; Dong, Buwen

2017-04-01

state can be controlled by prescribed, seasonally varying corrections to temperature and salinity, which substantially reduce SST biases without damping variability. This allows the present-day MetUM-GOML experiment to have a ocean mean state very close to the observed climatology (global RMSE ≈ 0.25°C). We perform three 150-year experiments with MetUM-GOML for (a) present-day (1976-2005 climatology) and for future scenarios with global-mean temperatures (b) 1.5°C and (c) 2.0°C above pre-industrial levels. For (b) and (c), we achieve these warming levels by increasing the CO2 concentrations in MetUM-GOML, as well as by adjusting the prescribed sea ice using change factors derived from a transient simulation with the fully coupled Met Office model. We analyse projected global and regional changes in temperature, precipitation and atmospheric circulation in our MetUM-GOML simulations, focusing on seasonal means, multi-annual persistence of seasonal extremes (e.g., the probability of consecutive wet summers) and intra-seasonal extremes (e.g., heatwaves, droughts, floods). To identify the influence of air-sea coupling on these projections, we compare the MetUM-GOML simulations to 150-year atmosphere-only simulations with prescribed daily SSTs from the corresponding MetUM-GOML runs. This comparison demonstrates whether atmosphere-ocean feedbacks influence the projections of changes hydro-meteorological extremes in a warmer world, as well as whether these feedbacks affect the assessment of the impacts avoided by limiting global-mean temperature change to 1.5°C. Our results will inform the choice of model framework for, and hence the experiment design of, further efforts to characterise the response to a fixed global-mean temperature increase, as well as future climate-change attribution experiments.

The potential role of sea spray droplets in facilitating air-sea gas transfer

Science.gov (United States)

Andreas, E. L.; Vlahos, P.; Monahan, E. C.

2016-05-01

For over 30 years, air-sea interaction specialists have been evaluating and parameterizing the role of whitecap bubbles in air-sea gas exchange. To our knowledge, no one, however, has studied the mirror image process of whether sea spray droplets can facilitate air-sea gas exchange. We are therefore using theory, data analysis, and numerical modeling to quantify the role of spray on air-sea gas transfer. In this, our first formal work on this subject, we seek the rate-limiting step in spray-mediated gas transfer by evaluating the three time scales that govern the exchange: τ air , which quantifies the rate of transfer between the atmospheric gas reservoir and the surface of the droplet; τ int , which quantifies the exchange rate across the air-droplet interface; and τ aq , which quantifies gas mixing within the aqueous solution droplet.

Updating sea spray aerosol emissions in the Community Multiscale Air Quality (CMAQ) model version 5.0.2

OpenAIRE

Gantt, B.; Kelly, J. T.; Bash, J. O.

2015-01-01

Sea spray aerosols (SSAs) impact the particle mass concentration and gas-particle partitioning in coastal environments, with implications for human and ecosystem health. Model evaluations of SSA emissions have mainly focused on the global scale, but regional-scale evaluations are also important due to the localized impact of SSAs on atmospheric chemistry near the coast. In this study, SSA emissions in the Community Multiscale Air Quality (CMAQ) model were updated to enhance the...

The Coral Reef Temperature Anomaly Database (CoRTAD) Version 5 - Global, 4 km Sea Surface Temperature and Related Thermal Stress Metrics for 1982-2012 (NCEI Accession 0126774)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Version 5 of the Coral Reef Temperature Anomaly Database (CoRTAD) is a global, 4 km, sea surface temperature (SST) and related thermal stress metrics dataset for...

Sea anemones may thrive in a high CO2 world.

Science.gov (United States)

Suggett, David J; Hall-Spencer, Jason M; Rodolfo-Metalpa, Riccardo; Boatman, Toby G; Payton, Ross; Tye Pettay, D; Johnson, Vivienne R; Warner, Mark E; Lawson, Tracy

2012-10-01

Increased seawater pCO 2 , and in turn 'ocean acidification' (OA), is predicted to profoundly impact marine ecosystem diversity and function this century. Much research has already focussed on calcifying reef-forming corals (Class: Anthozoa) that appear particularly susceptible to OA via reduced net calcification. However, here we show that OA-like conditions can simultaneously enhance the ecological success of non-calcifying anthozoans, which not only play key ecological and biogeochemical roles in present day benthic ecosystems but also represent a model organism should calcifying anthozoans exist as less calcified (soft-bodied) forms in future oceans. Increased growth (abundance and size) of the sea anemone (Anemonia viridis) population was observed along a natural CO 2 gradient at Vulcano, Italy. Both gross photosynthesis (P G ) and respiration (R) increased with pCO 2 indicating that the increased growth was, at least in part, fuelled by bottom up (CO 2 stimulation) of metabolism. The increase of P G outweighed that of R and the genetic identity of the symbiotic microalgae (Symbiodinium spp.) remained unchanged (type A19) suggesting proximity to the vent site relieved CO 2 limitation of the anemones' symbiotic microalgal population. Our observations of enhanced productivity with pCO 2 , which are consistent with previous reports for some calcifying corals, convey an increase in fitness that may enable non-calcifying anthozoans to thrive in future environments, i.e. higher seawater pCO 2 . Understanding how CO 2 -enhanced productivity of non- (and less-) calcifying anthozoans applies more widely to tropical ecosystems is a priority where such organisms can dominate benthic ecosystems, in particular following localized anthropogenic stress. © 2012 Blackwell Publishing Ltd.

Man -made greenhouse gases trigger unified force to start global warming impacts referred to as climate change

International Nuclear Information System (INIS)

Karishnan, K.J.; Kalam, A.

2011-01-01

Global warming problems due to man-made greenhouse gases (GHGs), appear to be a serious concern and threat to the globe. CO/sub 2/, O/sub 3, NOx and HFC's are the main greenhouse gases and CO/sub 2/ is one of the main cause of global warming. CO/sub 2/ is emitted from burning fossil fuels to produce electricity from power plants and burning of gasoline in vehicles and airplanes. Global greenhouse gases and its sources in regions are discussed in this paper. This paper initially discusses the CO/sub 2/ emissions and the recycle of CO/sub 2/ in biodiesel. This paper mainly focuses on 'Unified Force'. The increase of H/sub 2/O in the sea due to warming of the globe triggers the 'Unified Force' or 'Self-Compressive Surrounding Pressure Force' which is proportional to the H/sub 2/O level in the sea to start global warming impacts referred to as climate change. This paper also points out the climate change and the ten surprising results of global warming. Finally, this paper suggests switching from fossil fuel technology to green energy technologies like biodiesel which recycles CO/sub 2/ emissions and also Hydrogen Energy and Fuel Cell Technologies which eradicates global warming impacts. The benefits of switching from fossil fuel to biodiesel and Hydrogen Energy utilization includes reduction of greenhouse gas emissions and pollution, economic independence by having distributed production and burning of biodiesel does not add extra CO/sub 2/ to the air that contributes global warming impacts. (author)

Experimental and modeling study on effects of N2 and CO2 on ignition characteristics of methane/air mixture

Directory of Open Access Journals (Sweden)

Wen Zeng

2015-03-01

Full Text Available The ignition delay times of methane/air mixture diluted by N2 and CO2 were experimentally measured in a chemical shock tube. The experiments were performed over the temperature range of 1300–2100 K, pressure range of 0.1–1.0 MPa, equivalence ratio range of 0.5–2.0 and for the dilution coefficients of 0%, 20% and 50%. The results suggest that a linear relationship exists between the reciprocal of temperature and the logarithm of the ignition delay times. Meanwhile, with ignition temperature and pressure increasing, the measured ignition delay times of methane/air mixture are decreasing. Furthermore, an increase in the dilution coefficient of N2 or CO2 results in increasing ignition delays and the inhibition effect of CO2 on methane/air mixture ignition is stronger than that of N2. Simulated ignition delays of methane/air mixture using three kinetic models were compared to the experimental data. Results show that GRI_3.0 mechanism gives the best prediction on ignition delays of methane/air mixture and it was selected to identify the effects of N2 and CO2 on ignition delays and the key elementary reactions in the ignition chemistry of methane/air mixture. Comparisons of the calculated ignition delays with the experimental data of methane/air mixture diluted by N2 and CO2 show excellent agreement, and sensitivity coefficients of chain branching reactions which promote mixture ignition decrease with increasing dilution coefficient of N2 or CO2.

Different nature of glacial CaCO3 constituents between MIS 2 and MIS 12 in the East Sea/Japan Sea and its paleoceanographic implication

Science.gov (United States)

Khim, Boo-Keun; Tada, Ryuji; Itaki, Takuya

2014-05-01

Two piston cores (PC-05 and PC-08) were collected on the Yamato Rise in the East Sea/Japan Sea during the KR07-12 cruise. A composite core was achieved with the successful replacement of almost half of the upper part of core PC-05 by the entirety of core PC-08 based on the co-equivalence of L* values and the dark layers, because an interval (170 cm to 410 cm) of core PC-05 was considerably disturbed due to fluidization during the core execution. Chronostratigraphy of the composite core was constructed by the direct comparison of L* values to the well-dated core MD01-2407 that was obtained in the Oki Ridge. The lower-bottom of the composite core reached back to Marine Isotope Stage (MIS) 14, based on the age estimate by LR04 stacks. Downcore opal variation of the composite core exhibited the distinct orbital-scale cyclic changes; high during the interglacial and low during the glacial periods. However, downcore CaCO3 variation showed no corresponding orbital-scale cyclic change between glacial and interglacial periods. Some intervals of both periods were high in CaCO3 content. Frequent and large fluctuations in CaCO3 content seemed to be more related to the presence of dark layers containing thin lamination (TL) within the glacial and interglacial intervals. It is worthy to note that MIS 2 and MIS 12 are characterized by distinctly high CaCO3 content, showing up to 18% and 73%, respectively, among the glacial periods. Furthermore, in terms of lithology, MIS 2 was characterized by a thick dark layer (low L* values) with TL, whereas MIS 12 preserved the distinctly light layer (high L* values) with parallel laminations. Another remarkable dissimilarity between MIS 2 and MIS 12 was the nature of their CaCO3 constituent; the CaCO3 constituent of MIS 2 consisted of mostly planktonic foraminifera, whereas that of MIS 12 was mostly dump of coccolithophorids, regardless the presence of planktonic foraminifera. The distinctness of the CaCO3 constituents between MIS 2 and MIS

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

Wind Speed and Sea State Dependencies of Air-Sea Gas Transfer: Results From the High Wind Speed Gas Exchange Study (HiWinGS)

Science.gov (United States)

Blomquist, B. W.; Brumer, S. E.; Fairall, C. W.; Huebert, B. J.; Zappa, C. J.; Brooks, I. M.; Yang, M.; Bariteau, L.; Prytherch, J.; Hare, J. E.; Czerski, H.; Matei, A.; Pascal, R. W.

2017-10-01

A variety of physical mechanisms are jointly responsible for facilitating air-sea gas transfer through turbulent processes at the atmosphere-ocean interface. The nature and relative importance of these mechanisms evolves with increasing wind speed. Theoretical and modeling approaches are advancing, but the limited quantity of observational data at high wind speeds hinders the assessment of these efforts. The HiWinGS project successfully measured gas transfer coefficients (k660) with coincident wave statistics under conditions with hourly mean wind speeds up to 24 m s-1 and significant wave heights to 8 m. Measurements of k660 for carbon dioxide (CO2) and dimethylsulfide (DMS) show an increasing trend with respect to 10 m neutral wind speed (U10N), following a power law relationship of the form: k660 CO2˜U10N1.68 and k660 dms˜U10N1.33. Among seven high wind speed events, CO2 transfer responded to the intensity of wave breaking, which depended on both wind speed and sea state in a complex manner, with k660 CO2 increasing as the wind sea approaches full development. A similar response is not observed for DMS. These results confirm the importance of breaking waves and bubble injection mechanisms in facilitating CO2 transfer. A modified version of the Coupled Ocean-Atmosphere Response Experiment Gas transfer algorithm (COAREG ver. 3.5), incorporating a sea state-dependent calculation of bubble-mediated transfer, successfully reproduces the mean trend in observed k660 with wind speed for both gases. Significant suppression of gas transfer by large waves was not observed during HiWinGS, in contrast to results from two prior field programs.

Large divergence of satellite and Earth system model estimates of global terrestrial CO2 fertilization

Science.gov (United States)

Smith, W. Kolby; Reed, Sasha C.; Cleveland, Cory C.; Ballantyne, Ashley P; Anderegg, William R. L.; Wieder, William R.; Liu, Yi Y; Running, Steven W.

2015-01-01

Atmospheric mass balance analyses suggest that terrestrial carbon (C) storage is increasing, partially abating the atmospheric [CO2] growth rate, although the continued strength of this important ecosystem service remains uncertain. Some evidence suggests that these increases will persist owing to positive responses of vegetation growth (net primary productivity; NPP) to rising atmospheric [CO2] (that is, ‘CO2 fertilization’). Here, we present a new satellite-derived global terrestrial NPP data set, which shows a significant increase in NPP from 1982 to 2011. However, comparison against Earth system model (ESM) NPP estimates reveals a significant divergence, with satellite-derived increases (2.8 ± 1.50%) less than half of ESM-derived increases (7.6  ±  1.67%) over the 30-year period. By isolating the CO2 fertilization effect in each NPP time series and comparing it against a synthesis of available free-air CO2 enrichment data, we provide evidence that much of the discrepancy may be due to an over-sensitivity of ESMs to atmospheric [CO2], potentially reflecting an under-representation of climatic feedbacks and/or a lack of representation of nutrient constraints. Our understanding of CO2 fertilization effects on NPP needs rapid improvement to enable more accurate projections of future C cycle–climate feedbacks; we contend that better integration of modelling, satellite and experimental approaches offers a promising way forward.

Problems in the Relationship between CO2 Emissions and Global Warming

Directory of Open Access Journals (Sweden)

Ferenc Kovács

2005-03-01

Full Text Available In the analysis of environmental conditions and impacts, the viewpoint that greenhouse gases, primarily anthropogenic (industrial, human carbon dioxide, play a determining role in the change of global temperatures, ( the increase experienced in the last one and a half decade, has been given widespread publicity recently. Coal-fired power plants are the first to blame for the increase in atmospheric CO2 concentrations in the last two centuries. The study indicates possibilities to increase the efficiency of coal-fired power plants, which would involve a considerable reduction in CO2 emissions with an identical production volume of electrical energy. On the basis of the analysis of the amount of fossil fuels used, the amount of CO2 emissions and changes in the concentrations of atmospheric CO2, it is shown that no correlation can be proved between the factors investigated and changes in global temperatures.

Global warming and sea level rise. Chikyu Ondanka to kaimen josho

Energy Technology Data Exchange (ETDEWEB)

Mimura, N [Ibaraki University, Ibaraki (Japan). Faculty of Engineering

1993-10-15

This paper describes the following matters on the problems of global warming and sea level rise. The first evaluation report published by the inter-government panel on climate change (IPCC) in 1990 estimates that, if emission of greenhouse effect gas keeps increasing at the present rate, the air temperature and the average sea level would rise by 3[degree]C and 65 centimeters, respectively by 2100. Global warming would not only result in rise of the sea level, but also accompany changes in strengths and routes of tropical low pressure areas, and precipitation patterns. Downstream areas of large rivers and island countries on coral reefs may have a risk of getting submerged. Countries having coasts developed to high densities (Japan, for example) would be subjected to a high potential effect. An 'East Hemisphere International Conference on Sea Level Rising Problem' was held in Japan in August 1993 as part of the works to prepare the second evaluation report of the IPCC (publication scheduled for 1995). The conference was attended by 24 countries, and 43 study results were reported. 4 figs.

A cost effective CO2 strategy

DEFF Research Database (Denmark)

, a scenario-part and a cost-benefit part. Air and sea modes are not analyzed. The model adopts a bottom-up approach to allow a detailed assessment of transport policy measures. Four generic areas of intervention were identified and the likely effect on CO2 emissions, socioeconomic efficiency and other...... are evaluated according to CO2 reduction potential and according to the ‘shadow price’ on a reduction of one ton CO2. The shadow price reflects the costs (and benefits) of the different measures. Comparing the measures it is possible to identify cost effective measures, but these measures are not necessarily...... by the Ministry of Transport, with the Technical University of Denmark as one of the main contributors. The CO2-strategy was to be based on the principle of cost-effectiveness. A model was set up to assist in the assessment. The model consists of a projection of CO2-emissions from road and rail modes from 2020...

Trading Off Global Fuel Supply, CO2 Emissions and Sustainable Development.

Directory of Open Access Journals (Sweden)

Liam Wagner

Full Text Available The United Nations Conference on Climate Change (Paris 2015 reached an international agreement to keep the rise in global average temperature 'well below 2°C' and to 'aim to limit the increase to 1.5°C'. These reductions will have to be made in the face of rising global energy demand. Here a thoroughly validated dynamic econometric model (Eq 1 is used to forecast global energy demand growth (International Energy Agency and BP, which is driven by an increase of the global population (UN, energy use per person and real GDP (World Bank and Maddison. Even relatively conservative assumptions put a severe upward pressure on forecast global energy demand and highlight three areas of concern. First, is the potential for an exponential increase of fossil fuel consumption, if renewable energy systems are not rapidly scaled up. Second, implementation of internationally mandated CO2 emission controls are forecast to place serious constraints on fossil fuel use from ~2030 onward, raising energy security implications. Third is the challenge of maintaining the international 'pro-growth' strategy being used to meet poverty alleviation targets, while reducing CO2 emissions. Our findings place global economists and environmentalists on the same side as they indicate that the scale up of CO2 neutral renewable energy systems is not only important to protect against climate change, but to enhance global energy security by reducing our dependence of fossil fuels and to provide a sustainable basis for economic development and poverty alleviation. Very hard choices will have to be made to achieve 'sustainable development' goals.

Trading Off Global Fuel Supply, CO2 Emissions and Sustainable Development.

Science.gov (United States)

Wagner, Liam; Ross, Ian; Foster, John; Hankamer, Ben

2016-01-01

The United Nations Conference on Climate Change (Paris 2015) reached an international agreement to keep the rise in global average temperature 'well below 2°C' and to 'aim to limit the increase to 1.5°C'. These reductions will have to be made in the face of rising global energy demand. Here a thoroughly validated dynamic econometric model (Eq 1) is used to forecast global energy demand growth (International Energy Agency and BP), which is driven by an increase of the global population (UN), energy use per person and real GDP (World Bank and Maddison). Even relatively conservative assumptions put a severe upward pressure on forecast global energy demand and highlight three areas of concern. First, is the potential for an exponential increase of fossil fuel consumption, if renewable energy systems are not rapidly scaled up. Second, implementation of internationally mandated CO2 emission controls are forecast to place serious constraints on fossil fuel use from ~2030 onward, raising energy security implications. Third is the challenge of maintaining the international 'pro-growth' strategy being used to meet poverty alleviation targets, while reducing CO2 emissions. Our findings place global economists and environmentalists on the same side as they indicate that the scale up of CO2 neutral renewable energy systems is not only important to protect against climate change, but to enhance global energy security by reducing our dependence of fossil fuels and to provide a sustainable basis for economic development and poverty alleviation. Very hard choices will have to be made to achieve 'sustainable development' goals.

Air-sea exchange fluxes of synthetic polycyclic musks in the North Sea and the Arctic.

Science.gov (United States)

Xie, Zhiyong; Ebinghaus, Ralf; Temme, Christian; Heemken, Olaf; Ruck, Wolfgang

2007-08-15

Synthetic polycyclic musk fragrances Galaxolide (HHCB) and Tonalide (AHTN) were measured simultaneously in air and seawater in the Arctic and the North Sea and in the rural air of northern Germany. Median concentrations of gas-phase HHCB and AHTN were 4 and 18 pg m(-3) in the Arctic, 28 and 18 pg m(-3) in the North Sea, and 71 and 21 pg m(-3) in northern Germany, respectively. Various ratios of HHCB/AHTN implied that HHCB is quickly removed by atmospheric degradation, while AHTN is relatively persistent in the atmosphere. Dissolved concentrations ranged from 12 to 2030 pg L(-1) for HHCB and from below the method detection limit (3 pg L(-1)) to 965 pg L(-1) for AHTN with median values of 59 and 23 pg L(-1), respectively. The medians of volatilization fluxes for HHCB and AHTN were 27.2 and 14.2 ng m(-2) day(-1) and the depositional fluxes were 5.9 and 3.3 ng m(-2) day(-1), respectively, indicating water-to-air volatilization is a significant process to eliminate HHCB and AHTN from the North Sea. In the Arctic, deposition fluxes dominated the air-sea gas exchange of HHCB and AHTN, suggesting atmospheric input controls the levels of HHCB and AHTN in the polar region.

Change of properties after oxidation of IG-11 graphite by air and CO2 gas

International Nuclear Information System (INIS)

Lim, Yun-Soo; Chi, Se-Hwan; Cho, Kwang-Yun

2008-01-01

Artificial graphite is typically manufactured by carbonization of a shaped body of a kneaded mixture using granular cokes as a filler and pitch as a binder. It undergoes a pitch impregnation process if necessary and finally applying graphitization heat treatment. The effect of thermal oxidation in air or a CO 2 atmosphere on IG-11 graphite samples is investigated in this study. The results show a localized oxidation process that progressively reveals the large coke particles with increasing level of overall weight loss in air. The surface of the graphite was peeled off and no change was found in the specific gravity after air oxidation. However, the specific gravity of graphite was continuously decreased by CO 2 oxidation. The decrease in the specific gravity by CO 2 oxidation was due to CO 2 gas that progressed from the surface to the interior. The pore shape after CO 2 oxidation differed from that under air oxidation

Snowball Earth: Asynchronous coupling of sea-glacier flow with a global climate model

Science.gov (United States)

Pollard, D.; Kasting, J. F.; Zugger, M. E.

2017-05-01

During Snowball Earth episodes of the Neoproterozoic and Paleoproterozoic, limited amounts of tropical open ocean (Jormungand), or tropical ocean with thin ice cover, would help to explain (1) vigorous glacial activity in low latitudes, (2) survival of photosynthetic life, and (3) deglacial recovery without excessive buildup of atmospheric CO2. Some previous models have suggested that tropical open ocean or thin-ice cover is possible; however, its viability in the presence of kilometer-thick sea glaciers flowing from higher latitudes has not been demonstrated conclusively. Here we describe a new method of asynchronously coupling a zonal sea-glacier model with a 3-D global climate model and apply it to Snowball Earth. Equilibrium curves of ice line versus CO2 are mapped out, as well as their dependence on ocean heat transport efficiency, sea-glacier flow, and other model parameters. No climate states with limited tropical open ocean or thin ice are found in any of our model runs, including those with sea glaciers. If this result is correct, then other refugia such as cryoconite pans would have been required for life to survive. However, the reasons for the differences between our results and others should first be resolved. It is suggested that small-scale convective dynamics, affecting fractional snow cover in low latitudes, may be a critical factor accounting for these differences.

A high precision mass spectrometry method for measuring O2/N2 ratios and CO2 concentrations in air

International Nuclear Information System (INIS)

Marca, A.D.; Dennis, P.F.; Etchells, A.

2002-01-01

A full, detailed understanding of the global carbon budget is needed for robust modelling of global climate and environmental change. Since the industrial revolution the carbon cycle has been shifted from a steady state in which removal of CO 2 from the atmosphere through photosynthesis is balanced by its addition through respiration. Currently increased respiration due to deforestation, modern agricultural practises and the burning of fossil fuels dominates photosynthesis resulting in modern atmospheric CO 2 concentrations some 32% higher than the year 1800 levels. However, the CO 2 concentration rises are lower than expected from known fossil fuel combustion inventories. A significant proportion of the excess CO 2 is taken up by the oceans, however a missing carbon sink must still be invoked to account for the difference between measured and expected CO 2 rises. A global greening as a result of increased photosynthesis is required to close the circle

Estimation of air-sea CO2 flux in the coastal waters of Visakhapatnam

Digital Repository Service at National Institute of Oceanography (India)

Latha, T.P.; Rao, K.H.; Sarma, V.V.S.S.; Seetaram, P.; Choudhury, S.B.; Nagamani, P.V.; Dutt, B.S.; Dhadwal, V.K.; Manna, S.

radiation, humidity, wind speed, direction and gust were measured using AWS (Watch Dog, 2000 series) instrument which was mounted on the top of the boat. The atmospheric CO2 was measured using Li-COR 840A. The partial pressure of carbon dioxide (pCO2...

The contribution of ship emissions to air pollution in the North Sea regions

Energy Technology Data Exchange (ETDEWEB)

Matthias, Volker, E-mail: volker.matthias@gkss.d [GKSS Research Centre Geesthacht, Institute for Coastal Research, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Bewersdorff, Ines [GKSS Research Centre Geesthacht, Institute for Coastal Research, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Aulinger, Armin, E-mail: armin.aulinger@gkss.d [GKSS Research Centre Geesthacht, Institute for Coastal Research, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Quante, Markus, E-mail: markus.quante@gkss.d [GKSS Research Centre Geesthacht, Institute for Coastal Research, Max-Planck-Strasse 1, 21502 Geesthacht (Germany)

2010-06-15

As a consequence of the global distribution of manufacturing sites and the increasing international division of labour, ship traffic is steadily increasing and is becoming more and more important as an origin of air pollution. This study investigates the impact of ship emissions in coastal areas of the North Sea under conditions of the year 2000 by means of a regional chemistry transport model which runs on a sufficiently high resolution to study air pollution in coastal regions. It was found that northern Germany and Denmark in summer suffer from more than 50% higher sulphate, nitrate and ammonium aerosol concentrations due to contributions from ships. The implementation of a sulphur emission control area (SECA) in the North Sea, as it was implemented at the end of 2007, directly results in reduced sulphur dioxide and sulphate aerosol concentrations while nitrate aerosol concentrations are slightly increased. - Ship emissions lead to significantly enhanced air pollution by secondary inorganic aerosols in North Sea coastal areas.

Effectiveness of carbon dioxide removal in lowering atmospheric CO2 and reversing global warming in the context of 1.5 degrees

Science.gov (United States)

Zickfeld, K.; Azevedo, D.

2017-12-01

The majority of emissions scenarios that limit warming to 2°C, and nearly all emission scenarios that do not exceed 1.5°C warming by the year 2100 require artificial removal of CO2 from the atmosphere. Carbon dioxide removal (CDR) technologies in these scenarios are required to offset emissions from sectors that are difficult or costly to decarbonize and to generate global `net negative' emissions, allowing to compensate for earlier emissions and to meet long-term climate stabilization targets after overshoot. Only a few studies have explored the Earth system response to CDR and large uncertainties exist regarding the effect of CDR on the carbon cycle and its effectiveness in reversing climate impacts after overshoot. Here we explore the effectiveness of CDR in lowering atmospheric CO2 ("carbon cycle effectiveness") and cool global climate ("cooling effectiveness"). We force the University of Victoria Earth System Climate Model, a model of intermediate complexity, with a set of negative CO2 emissions pulses of different magnitude and applied from different background atmospheric CO2 concentrations. We find the carbon cycle effectiveness of CDR - defined as the change in atmospheric CO2 per unit CO2 removed - decreases with the amount of CO2 removed from the atmosphere and increases at higher background CO2 concentrations from which CDR is applied due to nonlinear responses of carbon sinks to CO2 and climate. The cooling effectiveness - defined as the change in global mean surface air temperature per unit CO2 removed - on the other hand, is largely insensitive to the amount of CO2 removed, but decreases if CDR is applied at higher atmospheric CO2 concentrations, due to the logarithmic relationship between atmospheric CO2 and radiative forcing. Based on our results we conclude that CDR is more effective in restoring a lower atmospheric CO2 concentration and reversing impacts directly linked to CO2 at lower levels of overshoot. CDR's effectiveness in restoring a

The Global Land-Ocean Temperature Index in Relation to Sunspot Number, the Atlantic Multidecadal Oscillation Index, the Mauna Loa Atmospheric Concentration of CO2, and Anthropogenic Carbon Emissions

Science.gov (United States)

Wilson, Robert M.

2013-01-01

Global warming/climate change has been a subject of scientific interest since the early 19th century. In particular, increases in the atmospheric concentration of carbon dioxide (CO2) have long been thought to account for Earth's increased warming, although the lack of a dependable set of observational data was apparent as late as the mid 1950s. However, beginning in the late 1950s, being associated with the International Geophysical Year, the opportunity arose to begin accurate continuous monitoring of the Earth's atmospheric concentration of CO2. Consequently, it is now well established that the atmospheric concentration of CO2, while varying seasonally within any particular year, has steadily increased over time. Associated with this rising trend in the atmospheric concentration of CO2 is a rising trend in the surface-air and sea-surface temperatures (SSTs). This Technical Publication (TP) examines the statistical relationships between 10-year moving averages (10-yma) of the Global Land-Ocean Temperature Index (GLOTI), sunspot number (SSN), the Atlantic Multidecadal Oscillation (AMO) index, and the Mauna Loa CO2 (MLCO2) index for the common interval 1964-2006, where the 10-yma values are used to indicate trends in the data. Scatter plots using the 10-yma values between GLOTI and each of the other parameters are determined, both as single-variate and multivariate fits. Scatter plots are also determined for MLCO2 using single-variate and bivariate (BV) fits, based on the GLOTI alone and the GLOTI in combination with the AMO index. On the basis of the inferred preferential fits for MLCO2, estimates for MLCO2 are determined for the interval 1885-1964, thereby yielding an estimate of the preindustrial level of atmospheric concentration of CO2. Lastly, 10-yma values of MLCO2 are compared against 10-yma estimates of the total carbon emissions (TCE) to determine the likelihood that manmade sources of carbon emissions are indeed responsible for the recent warming now

Assessment of a new prototype hydrogel CO2 sensor; comparison with air tonometry

NARCIS (Netherlands)

ter Steege, W.F.; Herber, S.; Olthuis, Wouter; Bergveld, Piet; van den Berg, Albert; Kolkman, J.

2007-01-01

a>Abstract a>Objective Gastrointestinal ischemia is always accompanied by an increased luminal CO2. Currently, air tonometry is used to measure luminal CO2. To improve the response time a new sensor was developed, enabling continuous CO2 measurement. It consists of a pH-sensitive hydrogel which

The effects of Norwegian gas export on the global CO2 emission

International Nuclear Information System (INIS)

1996-01-01

This report analyses how a limitation of Norway's gas export might affect the global CO 2 emission. In principle, a reduction of this export can lead to decreased or increased CO 2 emission depending on changes in several conditions that individually have conflicting emission effects. What the total effect will be can only become clear after a thorough empirical analysis of the supply and demand structure. The model calculations presented in the report show that the global emission will probably increase if Norway reduces the gas export. A gas export reduction of 10 million tonne oil equivalents in 2015 will increase the global emission by 1.4 and 7.5 million tonne CO 2 depending on the assumption made for alternative gas supplies to the European market and for market conditions in the importing countries. 4 refs., 32 figs., 44 tabs

Southern Adriatic sea as a potential area for CO2 geological storage

International Nuclear Information System (INIS)

Volpi, V.; Forlin, F.; Donda, F.; Civile, D.; Facchin, L.; Sauli, L.; Merson, B.; Sinza-Mendieta, K.; Shams, A.

2015-01-01

The Southern Adriatic Sea is one of the five prospective areas for CO 2 storage being evaluated under the three year (FP7) European SiteChar project dedicated to the characterization of European CO 2 storage sites. The potential reservoir for CO 2 storage is represented by a carbonate formation, the wackstones and packstones of the Scaglia Formation (Upper Cretaceous-Paleogene). In this paper, we present the geological characterization and the 3D modeling that led to the identification of three sites, named Grazia, Rovesti and Grifone, where the Scaglia Formation, with an average thickness of 50 m, reveals good petrophysical characteristics and is overlain by an up to 1 200 thick cap-rock. The vicinity of the selected sites to the Enel - Federico II power plant (one of the major Italian CO 2 emitter) where a pilot plant for CO 2 capture has been already started in April 2010, represents a good opportunity to launch the first Carbon Capture and Storage (CCS) pilot project in Italy and to apply this technology at industrial level, strongly contributing at the same time at reducing the national CO 2 emissions. (authors)

Global Thermal Power Plants Database: Unit-Based CO2, SO2, NOX and PM2.5 Emissions in 2010

Science.gov (United States)

Tong, D.; Qiang, Z.; Davis, S. J.

2016-12-01

There are more than 30,000 thermal power plants now operating worldwide, reflecting a tremendously diverse infrastructure that includes units burning oil, natural gas, coal and biomass and ranging in capacity from 1GW. Although the electricity generated by this infrastructure is vital to economic activities across the world, it also produces more CO2 and air pollution emissions than any other industry sector. Here we present a new database of global thermal power-generating units and their emissions as of 2010, GPED (Global Power Emissions Database), including the detailed unit information of installed capacity, operation year, geographic location, fuel type and control measures for more than 70000 units. In this study, we have compiled, combined, and harmonized the available underlying data related to thermal power-generating units (e.g. eGRID of USA, CPED of China and published Indian power plants database), and then analyzed the generating capacity, capacity factor, fuel type, age, location, and installed pollution-control technology in order to determine those units with disproportionately high levels of emissions. In total, this work is of great importance for improving spatial distribution of global thermal power plants emissions and exploring their environmental impacts at global scale.

Sea-to-air and diapycnal nitrous oxide fluxes in the eastern tropical North Atlantic Ocean

Directory of Open Access Journals (Sweden)

A. Kock

2012-03-01

Full Text Available Sea-to-air and diapycnal fluxes of nitrous oxide (N₂O into the mixed layer were determined during three cruises to the upwelling region off Mauritania. Sea-to-air fluxes as well as diapycnal fluxes were elevated close to the shelf break, but elevated sea-to-air fluxes reached further offshore as a result of the offshore transport of upwelled water masses. To calculate a mixed layer budget for N₂O we compared the regionally averaged sea-to-air and diapycnal fluxes and estimated the potential contribution of other processes, such as vertical advection and biological N₂O production in the mixed layer. Using common parameterizations for the gas transfer velocity, the comparison of the average sea-to-air and diapycnal N₂O fluxes indicated that the mean sea-to-air flux is about three to four times larger than the diapycnal flux. Neither vertical and horizontal advection nor biological production were found sufficient to close the mixed layer budget. Instead, the sea-to-air flux, calculated using a parameterization that takes into account the attenuating effect of surfactants on gas exchange, is in the same range as the diapycnal flux. From our observations we conclude that common parameterizations for the gas transfer velocity likely overestimate the air-sea gas exchange within highly productive upwelling zones.

Brief communication: ikaite (CaCO3*6H2O) discovered in Arctic sea ice

Science.gov (United States)

Dieckmann, G. S.; Nehrke, G.; Uhlig, C.; Göttlicher, J.; Gerland, S.; Granskog, M. A.; Thomas, D. N.

2010-02-01

We report for the first time on the discovery of calcium carbonate crystals as ikaite (CaCO3*6H2O) in sea ice from the Arctic (Kongsfjorden, Svalbard). This finding demonstrates that the precipitation of calcium carbonate during the freezing of sea ice is not restricted to the Antarctic, where it was observed for the first time in 2008. This finding is an important step in the quest to quantify its impact on the sea ice driven carbon cycle and should in the future enable improvement parametrization sea ice carbon models.

Global change and the measurement of absolute sea-level

Science.gov (United States)

Diamante, John M.; Pyle, Thomas E.; Carter, William E.; Scherer, Wolfgang

To quantify properly the long-term response of sea-level to climate change, land motions must be separated from the apparent or relative sea-level change recorded by conventional tide/sea-level gauges. Here we present a concept for global measurement of the true or “absolute” sea-level change, which combines recent advances in space-based geodetic techniques with plans for a global sea-level network under the World Climate Research Programme (WCRP). Data from initial feasibility tests show that land motion, due to global (plate tectonic), regional (glacial rebound), or local (fluid withdrawal) effects, can probably be measured to ±1cm (on a single measurement basis) by an innovative combination of Very Long Baseline Interferometry (VLBI) and Global Positioning System (GPS) tevhniques. By making repeated observations of position at a number of tide gauges using portable, economical GPS receivers in a differential mode relative to the fewer, more stable, but more expensive VLBI observatories, it will be possible to subtract land motion from the relative sea-level signal. Decadal to century scale trends at the 1-2mm y -1 level will be resolvable in the sea-level and vertical land motion time series within about a decade. Detection of subsidence or uplift at specific gauges will allow correction for land motion or deletion of bad data when computing regional or global, i.e. eustatic, sea-level changes. In addition to their applications in oceanography and climate studies, such data will test models by Peltier and other that relate mantle viscosity and deglaciation history to present rates of crustal subsidence or uplift. If the predicted crustal motions are confirmed, we can also have more confidence in the use of historical tide/sea-level gauge records in retrospective studies of sea-level change related to climate variability on decadal or longer time scales. It is concluded that as few as one-third (about 100) of the total number of tide/sea-level gauges (250

Influence of the dissolution of increasing quantities of CO2 in the sea water

International Nuclear Information System (INIS)

Poitou, J.

2007-03-01

By the increase of carbon dioxide quantity in the atmosphere, the acidity of the ocean, which absorbs a part of this CO 2 , will increase. This acidity level is going to modify the shells and calcareous bases formation of many sea species. The author details the principle of the acidity evolution by the CO 2 increase, the consequences on the ocean fauna and the impacts for the humans. (A.L.B.)

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

Energy Technology Data Exchange (ETDEWEB)

Yager, P.L.

1996-12-31

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

Synergistic effects of pCO2 and iron availability on nutrient consumption ratio of the Bering Sea phytoplankton community

Directory of Open Access Journals (Sweden)

K. Sugie

2013-10-01

Full Text Available Little is known concerning the effect of CO2 on phytoplankton ecophysiological processes under nutrient and trace element-limited conditions, because most CO2 manipulation experiments have been conducted under elements-replete conditions. To investigate the effects of CO2 and iron availability on phytoplankton ecophysiology, we conducted an experiment in September 2009 using a phytoplankton community in the iron limited, high-nutrient, low-chlorophyll (HNLC region of the Bering Sea basin . Carbonate chemistry was controlled by the bubbling of the several levels of CO2 concentration (180, 380, 600, and 1000 ppm controlled air, and two iron conditions were established, one with and one without the addition of inorganic iron. We demonstrated that in the iron-limited control conditions, the specific growth rate and the maximum photochemical quantum efficiency (Fv/Fm of photosystem (PS II decreased with increasing CO2 levels, suggesting a further decrease in iron bioavailability under the high-CO2 conditions. In addition, biogenic silica to particulate nitrogen and biogenic silica to particulate organic carbon ratios increased from 2.65 to 3.75 and 0.39 to 0.50, respectively, with an increase in the CO2 level in the iron-limited controls. By contrast, the specific growth rate, Fv/Fm values and elemental compositions in the iron-added treatments did not change in response to the CO2 variations, indicating that the addition of iron canceled out the effect of the modulation of iron bioavailability due to the change in carbonate chemistry. Our results suggest that high-CO2 conditions can alter the biogeochemical cycling of nutrients through decreasing iron bioavailability in the iron-limited HNLC regions in the future.

Children's exposure to indoor air in urban nurseries-part I: CO{sub 2} and comfort assessment

Energy Technology Data Exchange (ETDEWEB)

Branco, P.T.B.S.; Alvim-Ferraz, M.C.M.; Martins, F.G.; Sousa, S.I.V., E-mail: sofia.sousa@fe.up.pt

2015-07-15

Indoor air quality (IAQ) in nurseries is an emerging case-study. Thus, this study, as the Part I of the larger study “Children's exposure to indoor air in urban nurseries”, aimed to: i) evaluate nurseries’ indoor concentrations of carbon dioxide (CO{sub 2}), a global IAQ indicator, in class and lunch rooms; ii) assess indoor comfort parameters–temperature (T) and relative humidity (RH); and iii) analyse them according to guidelines and references for IAQ, comfort and children's health. Indoor continuous measurements were performed. Non-compliances with guidelines were found in comfort parameters, which could cause discomfort situations and also microbial proliferation. Exceedances in CO{sub 2} concentrations were also found and they were caused by poor ventilation and high classroom occupation. More efficient ventilation and control of comfort parameters, as well as to reduce occupation by reviewing Portuguese legislation on that matter, would certainly improve IAQ and comfort in nurseries and consequently safeguard children's health. - Highlights: • High occupation and poor ventilation were main determinants of IAQ in nurseries. • T and RH indoor values found in nurseries are likely to cause thermal discomfort. • Building characteristics and an inadequate ventilation determined T and RH values. • High CO{sub 2} concentrations found could indicate accumulation of other air pollutants.

Cultivation of Chlorella Vulgaris Using Airlift Photobioreactor Sparged with 5%CO 2 -Air as a Biofixing Process

Directory of Open Access Journals (Sweden)

Mahmood Khazzal Hummadi AL-Mashhadani

2017-04-01

Full Text Available The present paper addresses cultivation of Chlorella vulgaris microalgae using airlift photobioreactor that sparged with 5% CO 2 /air. The experimental data were compared with that obtained from bioreactor aerated with air and unsparged bioreactor. The results showed that the concentration of biomass is 0.36 g l -1 in sparged bioreactor with CO2/air, while, the concentration of biomass reached to 0.069 g l -1 in the unsparged bioreactor. They showed also that aerated ioreactor.with CO2/air gives more biomass production even the bioreactor was aerated with air. This study proved that application of sparging system for ultivation of Chlorella vulgaris microalgae using either CO2/air mixture or air has a significant growth rate, since the bioreactors become more thermodynamically favorable and provide impetus for a higher level of production. biofixing process

Co-control of urban air pollutants and greenhouse gases in Mexico City.

Science.gov (United States)

West, J Jason; Osnaya, Patricia; Laguna, Israel; Martínez, Julia; Fernández, Adrián

2004-07-01

This study addresses the synergies of mitigation measures to control urban air pollutant and greenhouse gas (GHG) emissions, in developing integrated "co-control" strategies for Mexico City. First, existing studies of emissions reduction measures--PROAIRE (the air quality plan for Mexico City) and separate GHG studies--are used to construct a harmonized database of options. Second, linear programming (LP) is developed and applied as a decision-support tool to analyze least-cost strategies for meeting co-control targets for multiple pollutants. We estimate that implementing PROAIRE measures as planned will reduce 3.1% of the 2010 metropolitan CO2 emissions, in addition to substantial local air pollutant reductions. Applying the LP, PROAIRE emissions reductions can be met at a 20% lower cost, using only the PROAIRE measures, by adjusting investments toward the more cost-effective measures; lower net costs are possible by including cost-saving GHG mitigation measures, but with increased investment. When CO2 emission reduction targets are added to PROAIRE targets, the most cost-effective solutions use PROAIRE measures for the majority of local pollutant reductions, and GHG measures for additional CO2 control. Because of synergies, the integrated planning of urban-global co-control can be beneficial, but we estimate that for Mexico City these benefits are often small.

Air-sea interactions during strong winter extratropical storms

Science.gov (United States)

Nelson, Jill; He, Ruoying; Warner, John C.; Bane, John

2014-01-01

A high-resolution, regional coupled atmosphere–ocean model is used to investigate strong air–sea interactions during a rapidly developing extratropical cyclone (ETC) off the east coast of the USA. In this two-way coupled system, surface momentum and heat fluxes derived from the Weather Research and Forecasting model and sea surface temperature (SST) from the Regional Ocean Modeling System are exchanged via the Model Coupling Toolkit. Comparisons are made between the modeled and observed wind velocity, sea level pressure, 10 m air temperature, and sea surface temperature time series, as well as a comparison between the model and one glider transect. Vertical profiles of modeled air temperature and winds in the marine atmospheric boundary layer and temperature variations in the upper ocean during a 3-day storm period are examined at various cross-shelf transects along the eastern seaboard. It is found that the air–sea interactions near the Gulf Stream are important for generating and sustaining the ETC. In particular, locally enhanced winds over a warm sea (relative to the land temperature) induce large surface heat fluxes which cool the upper ocean by up to 2 °C, mainly during the cold air outbreak period after the storm passage. Detailed heat budget analyses show the ocean-to-atmosphere heat flux dominates the upper ocean heat content variations. Results clearly show that dynamic air–sea interactions affecting momentum and buoyancy flux exchanges in ETCs need to be resolved accurately in a coupled atmosphere–ocean modeling framework.

Global Sensitivity Analysis to Assess Salt Precipitation for CO2 Geological Storage in Deep Saline Aquifers

Directory of Open Access Journals (Sweden)

Yuan Wang

2017-01-01

Full Text Available Salt precipitation is generated near the injection well when dry supercritical carbon dioxide (scCO2 is injected into saline aquifers, and it can seriously impair the CO2 injectivity of the well. We used solid saturation (Ss to map CO2 injectivity. Ss was used as the response variable for the sensitivity analysis, and the input variables included the CO2 injection rate (QCO2, salinity of the aquifer (XNaCl, empirical parameter m, air entry pressure (P0, maximum capillary pressure (Pmax, and liquid residual saturation (Splr and Sclr. Global sensitivity analysis methods, namely, the Morris method and Sobol method, were used. A significant increase in Ss was observed near the injection well, and the results of the two methods were similar: XNaCl had the greatest effect on Ss; the effect of P0 and Pmax on Ss was negligible. On the other hand, with these two methods, QCO2 had various effects on Ss: QCO2 had a large effect on Ss in the Morris method, but it had little effect on Ss in the Sobol method. We also found that a low QCO2 had a profound effect on Ss but that a high QCO2 had almost no effect on the Ss value.

Physiological effects of environmental acidification in the deep-sea urchin Strongylocentrotus fragilis

Science.gov (United States)

Taylor, J. R.; Lovera, C.; Whaling, P. J.; Buck, K. R.; Pane, E. F.; Barry, J. P.

2014-03-01

Anthropogenic CO2 is now reaching depths over 1000 m in the Eastern Pacific, overlapping the Oxygen Minimum Zone (OMZ). Deep-sea animals are suspected to be especially sensitive to environmental acidification associated with global climate change. We have investigated the effects of elevated pCO2 and variable O2 on the deep-sea urchin Strongylocentrotus fragilis, a species whose range of 200-1200 m depth includes the OMZ and spans a pCO2 range of approx. 600-1200 μatm (approx. pH 7.6 to 7.8). Individuals were evaluated during two exposure experiments (1-month and 4 month) at control and three levels of elevated pCO2 at in situ O2 levels of approx. 10% air saturation. A treatment of control pCO2 at 100% air saturation was also included in experiment two. During the first experiment, perivisceral coelomic fluid (PCF) acid-base balance was investigated during a one-month exposure; results show S. fragilis has limited ability to compensate for the respiratory acidosis brought on by elevated pCO2, due in part to low non-bicarbonate PCF buffering capacity. During the second experiment, individuals were separated into fed and fasted experimental groups, and longer-term effects of elevated pCO2 and variable O2 on righting time, feeding, growth, and gonadosomatic index (GSI) were investigated for both groups. Results suggest that the acidosis found during experiment one does not directly correlate with adverse effects during exposure to realistic future pCO2 levels.

A multivariate analysis of Antarctic sea ice since 1979

Energy Technology Data Exchange (ETDEWEB)

Magalhaes Neto, Newton de; Evangelista, Heitor [Universidade do Estado do Rio de Janeiro (Uerj), LARAMG - Laboratorio de Radioecologia e Mudancas Globais, Maracana, Rio de Janeiro, RJ (Brazil); Tanizaki-Fonseca, Kenny [Universidade do Estado do Rio de Janeiro (Uerj), LARAMG - Laboratorio de Radioecologia e Mudancas Globais, Maracana, Rio de Janeiro, RJ (Brazil); Universidade Federal Fluminense (UFF), Dept. Analise Geoambiental, Inst. de Geociencias, Niteroi, RJ (Brazil); Penello Meirelles, Margareth Simoes [Universidade do Estado do Rio de Janeiro (UERJ)/Geomatica, Maracana, Rio de Janeiro, RJ (Brazil); Garcia, Carlos Eiras [Universidade Federal do Rio Grande (FURG), Laboratorio de Oceanografia Fisica, Rio Grande, RS (Brazil)

2012-03-15

Recent satellite observations have shown an increase in the total extent of Antarctic sea ice, during periods when the atmosphere and oceans tend to be warmer surrounding a significant part of the continent. Despite an increase in total sea ice, regional analyses depict negative trends in the Bellingshausen-Amundsen Sea and positive trends in the Ross Sea. Although several climate parameters are believed to drive the formation of Antarctic sea ice and the local atmosphere, a descriptive mechanism that could trigger such differences in trends are still unknown. In this study we employed a multivariate analysis in order to identify the response of the Antarctic sea ice with respect to commonly utilized climate forcings/parameters, as follows: (1) The global air surface temperature, (2) The global sea surface temperature, (3) The atmospheric CO{sub 2} concentration, (4) The South Annular Mode, (5) The Nino 3, (6) The Nino (3 + 4, 7) The Nino 4, (8) The Southern Oscillation Index, (9) The Multivariate ENSO Index, (10) the Total Solar Irradiance, (11) The maximum O{sub 3} depletion area, and (12) The minimum O{sub 3} concentration over Antarctica. Our results indicate that western Antarctic sea ice is simultaneously impacted by several parameters; and that the minimum, mean, and maximum sea ice extent may respond to a separate set of climatic/geochemical parameters. (orig.)

Return of the coral reef hypothesis: basin to shelf partitioning of CaCO3 and its effect on atmospheric CO2.

Science.gov (United States)

Opdyke, B N; Walker, J C

1992-08-01

Differences in the rate of coral reef carbonate deposition from the Pleistocene to the Holocene may account for the Quaternary variation of atmospheric CO2. Volumes of carbonate associated with Holocene reefs require an average deposition rate of 2.0 x 10(13) mol/yr for the past 5 ka. In light of combined riverine, midocean ridge, and ground-water fluxes of calcium to the oceans of 2.3 x 10(13) mol/yr, the current flux of calcium carbonate to pelagic sediments must be far below the Pleistocene average of 1.2 x 10(13) mol/yr. We suggest that sea-level change shifts the locus of carbonate deposition from the deep sea to the shelves as the normal glacial-interglacial pattern of deposition for Quaternary global carbonates. To assess the impact of these changes on atmospheric CO2, a simple numerical simulation of the global carbon cycle was developed. Atmospheric CO2 as well as calcite saturation depth and sediment responses to these carbonate deposition changes are examined. Atmospheric CO2 changes close to those observed in the Vostok ice core, approximately 80 ppm CO2, for the Quaternary are observed as well as the approximate depth changes in percent carbonate of sediments measured in the Pacific Ocean over the same time interval.

CO2-induced climate change in northern Europe: comparison of 12 CMIP2 experiments

International Nuclear Information System (INIS)

Raeisaenen, Jouni

2000-01-01

The results of 12 coupled atmosphere-ocean general circulation model experiments participating in the second phase of the Coupled Model Intercomparison Project (CMIP2) are studied with focus on the area of northern Europe. The variables considered are surface air temperature, precipitation and sea level pressure. The 80-year control simulations are first compared with observational estimates of the present climate. Several aspects of the simulated CO 2 -induced climate changes, defined by subtracting the control run seasonal or annual means from 20-year perturbation run means around the transient doubling of CO 2 , are then studied. The common features and individual variations in the simulated climate change are documented. Particular attention is put on expressing the inter experiment agreement in quantitative terms and on estimating the relative contribution of model-simulated internal variability to the inter experiment variance. For that purpose, a new statistical framework is developed. Finally, an attempt is made to statistically relate the inter experiment differences in the simulated climate change in northern Europe to aspects of the control climates, global climate change and some of the basic model characteristics. A summary of the main findings is given in the last section of the report

Field Observations of Coastal Air-Sea Interaction

Science.gov (United States)

Ortiz-Suslow, D. G.; Haus, B. K.; Williams, N. J.; Graber, H. C.

2016-12-01

In the nearshore zone wind, waves, and currents generated from different forcing mechanisms converge in shallow water. This can profoundly affect the physical nature of the ocean surface, which can significantly modulate the exchange of momentum, heat, and mass across the air-sea interface. For decades, the focus of air-sea interaction research has been on the open ocean while the shallow water regime has been relatively under-explored. This bears implications for efforts to understand and model various coastal processes, such as mixing, surface transport, and air-sea gas flux. The results from a recent study conducted at the New River Inlet in North Carolina showed that directly measured air-sea flux parameters, such as the atmospheric drag coefficient, are strong functions of space as well as the ambient conditions (i.e. wind speed and direction). The drag is typically used to parameterize the wind stress magnitude. It is generally assumed that the wind direction is the direction of the atmospheric forcing (i.e. wind stress), however significant wind stress steering off of the azimuthal wind direction was observed and was found to be related to the horizontal surface current shear. The authors have just returned from a field campaign carried out within Monterey Bay in California. Surface observations made from two research vessels were complimented by an array of beach and inland flux stations, high-resolution wind forecasts, and satellite image acquisitions. This is a rich data set and several case studies will be analyzed to highlight the importance of various processes for understanding the air-sea fluxes. Preliminary findings show that interactions between the local wind-sea and the shoaling, incident swell can have a profound effect on the wind stress magnitude. The Monterey Bay coastline contains a variety of topographical features and the importance of land-air-sea interactions will also be investigated.

Geological characterization of CO{sub 2} storage sites: lessons from Sleipner, Northern North Sea

Energy Technology Data Exchange (ETDEWEB)

R.A. Chadwick; P. Zweigel; U. Gregersen; G.A. Kirby; S. Holloway; P.N. Johannessen [British Geological Survey, Keyworth (United Kingdom). Kingsley Dunham Centre

2003-07-01

The paper aims to draw some generic conclusions on reservoir characterization based on the Sleipner operation in the North Sea where CO{sub 2} is being injected into the Utsira Sand, a saline aquifer. Regional mapping and petrophysical characterization of the reservoir, based on 2D seismic and well data, enable gross storage potential to be evaluated. Site specific injection studies, however, require precision depth mapping based on 3D seismic data and detailed knowledge of reservoir stratigraphy. Stratigraphical and structural permeability barriers, difficult to detect prior to CO{sub 2} injection, can radically affect CO{sub 2} migration within the aquifer. 5 refs., 5 figs.

Global sea turtle conservation successes.