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

NASA Astrophysics Data System (ADS)

McNeil, B.

2016-02-01

Elevated carbon dioxide concentrations in seawater (hypercapnia) can induce neurological, physiological and behavioural deficiencies in marine animals. Prediction of the onset and evolution of hypercapnia in the ocean requires a good understanding of annual oceanic carbon dioxide variability, but relevant global observational data are sparse. Here we diagnose global ocean patterns of monthly carbon variability based on observations that allow us to examine the evolution of surface ocean CO2 levels over the entire annual cycle under increasing atmospheric CO2 concentrations. We find that some oceanic regions undergo an up to 10-fold amplification of the natural cycle of CO2 by 2100, if atmospheric carbon dioxide concentrations continue to rise throughout this century (RCP8.5). Projections from a suite of Earth System Climate Models are broadly consistent with the findings from our data based approach. Our predicted amplification in the annual CO2 cycle displays distinct global patterns that may expose major fisheries in the Southern, Pacific and North Atlantic Oceans to high CO2 events many decades earlier than expected from average atmospheric CO2 concentrations. We suggest that these ocean 'CO2 hotspots' evolve as a combination of the strong seasonal dynamics of CO2 and the long-term effective storage of anthropogenic CO2 that lowers the buffer capacity in those regions, causing a non-linear CO2 amplification over the annual cycle. The onset of ocean hypercapnia events (pCO2 >1000 µatm) is forecast for atmospheric CO2 concentrations that exceed 650 ppm, with hypercapnia spreading to up to one half of the surface ocean by the year 2100 under a high-emissions scenario (RCP8.5) with potential implications for fisheries over the coming century.

Are changes in the phytoplankton community structure altering the flux of CO2 in regions of the North Atlantic?

NASA Astrophysics Data System (ADS)

Ostle, C.; Landschutzer, P.; Johnson, M.; Schuster, U.; Watson, A. J.; Edwards, M.; Robinson, C.

2016-02-01

The North Atlantic Ocean is a globally important sink of carbon dioxide (CO2). However, the strength of the sink varies temporally and regionally. This study uses a neural network method to map the surface ocean pCO2 (partial pressure of CO2) and flux of CO2from the atmosphere to the ocean alongside measurements of plankton abundance collected from the Continuous Plankton Recorder (CPR) survey to determine the relationship between regional changes in phytoplankton community structure and regional differences in carbon flux. Despite increasing sea surface temperatures, the Grand Banks of Newfoundland show a decrease in sea surface pCO2 of -2 µatm yr-1 from 1993 to 2011. The carbon flux in the North Sea is variable over the same period. This is in contrast to most of the open ocean within the North Atlantic, where increases in sea surface pCO2 follow the trend of increasing CO2 in the atmosphere, i.e. the flux or sink remains constant. The increasing CO2 sink in the Grand Banks of Newfoundland and the variable sink in the North Sea correlate with changes in phytoplankton community composition. This study investigates the biogeochemical and oceanographic mechanisms potentially linking increasing sea surface temperature, changes in phytoplankton community structure and the changing carbon sink in these two important regions of the Atlantic Ocean. The use of volunteer ships to concurrently collect these datasets demonstrates the potential to investigate relationships between plankton community structure and carbon flux in a cost-effective way. These results not only have implications for plankton-dynamic biogeochemical models, but also likely influence carbon export, as different phytoplankton communities have different carbon export efficiencies. Extending and maintaining such datasets is critical to improving our understanding of and monitoring carbon cycling in the surface ocean and improving climate model accuracy.

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

NASA Astrophysics Data System (ADS)

Bakker, D. C. E.; Pfeil, B.; Smith, K.; Hankin, S.; Olsen, A.; Alin, S. R.; Cosca, C.; Harasawa, S.; Kozyr, A.; Nojiri, Y.; O'Brien, K. M.; Schuster, U.; Telszewski, M.; Tilbrook, B.; Wada, C.; Akl, J.; Barbero, L.; Bates, N.; Boutin, J.; Cai, W.-J.; Castle, R. D.; Chavez, F. P.; Chen, L.; Chierici, M.; Currie, K.; de Baar, H. J. W.; Evans, W.; Feely, R. A.; Fransson, A.; Gao, Z.; Hales, B.; Hardman-Mountford, N.; Hoppema, M.; Huang, W.-J.; Hunt, C. W.; Huss, B.; Ichikawa, T.; Johannessen, T.; Jones, E. M.; Jones, S. D.; Jutterström, S.; Kitidis, V.; Körtzinger, A.; Landschtzer, P.; Lauvset, S. K.; Lefèvre, N.; Manke, A. B.; Mathis, J. T.; Merlivat, L.; Metzl, N.; Murata, A.; Newberger, T.; Ono, T.; Park, G.-H.; Paterson, K.; Pierrot, D.; Ríos, A. F.; Sabine, C. L.; Saito, S.; Salisbury, J.; Sarma, V. V. S. S.; Schlitzer, R.; Sieger, R.; Skjelvan, I.; Steinhoff, T.; Sullivan, K.; Sun, H.; Sutton, A. J.; Suzuki, T.; Sweeney, C.; Takahashi, T.; Tjiputra, J.; Tsurushima, N.; van Heuven, S. M. A. C.; Vandemark, D.; Vlahos, P.; Wallace, D. W. R.; Wanninkhof, R.; Watson, A. J.

2013-08-01

The Surface Ocean CO2 Atlas (SOCAT) is an effort by the international marine carbon research community. It aims to improve access to carbon dioxide measurements in the surface oceans by regular releases of quality controlled and fully documented synthesis and gridded fCO2 (fugacity of carbon dioxide) products. SOCAT version 2 presented here extends the data set for the global oceans and coastal seas by four years and has 10.1 million surface water fCO2 values from 2660 cruises between 1968 and 2011. The procedures for creating version 2 have been comparable to those for version 1. The SOCAT website (http://www.socat.info/) provides access to the individual cruise data files, as well as to the synthesis and gridded data products. Interactive online tools allow visitors to explore the richness of the data. Scientific users can also retrieve the data as downloadable files or via Ocean Data View. Version 2 enables carbon specialists to expand their studies until 2011. Applications of SOCAT include process studies, quantification of the ocean carbon sink and its spatial, seasonal, year-to-year and longer-term variation, as well as initialisation or validation of ocean carbon models and coupled-climate carbon models.

Nonuniform ocean acidification and attenuation of the ocean carbon sink

NASA Astrophysics Data System (ADS)

Fassbender, Andrea J.; Sabine, Christopher L.; Palevsky, Hilary I.

2017-08-01

Surface ocean carbon chemistry is changing rapidly. Partial pressures of carbon dioxide gas (pCO2) are rising, pH levels are declining, and the ocean's buffer capacity is eroding. Regional differences in short-term pH trends primarily have been attributed to physical and biological processes; however, heterogeneous seawater carbonate chemistry may also be playing an important role. Here we use Surface Ocean CO2 Atlas Version 4 data to develop 12 month gridded climatologies of carbonate system variables and explore the coherent spatial patterns of ocean acidification and attenuation in the ocean carbon sink caused by rising atmospheric pCO2. High-latitude regions exhibit the highest pH and buffer capacity sensitivities to pCO2 increases, while the equatorial Pacific is uniquely insensitive due to a newly defined aqueous CO2 concentration effect. Importantly, dissimilar regional pH trends do not necessarily equate to dissimilar acidity ([H+]) trends, indicating that [H+] is a more useful metric of acidification.

pCO2 and CO2 Exchange During High Bora Winds in the Northern Adriatic

DTIC Science & Technology

2013-03-05

coastal ocean , has not been adequately assessed. Here we show the response of surfacewater pCO2 and CO2 fluxes during high borawind in the Northern...m−2 day−1 day in thewinter cases and 29 mmol m−2 day−1 in the summer case) over themag- nitude of the mean annual value. Oceanic data measured...simultaneously to surface pCO2 measurements suggest that themost likely responsiblemechanisms for the observed pCO2 increaseswere oceanic verticalmixing and

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

DOE Office of Scientific and Technical Information (OSTI.GOV)

Levi, A.; Sasselov, D.; Podolak, M., E-mail: amitlevi.planetphys@gmail.com

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

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

NASA Astrophysics Data System (ADS)

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 likelihood of satisfying growing global energy demand while helping to stabilize or reduce atmospheric CO2 and its impacts. Policies supporting the search and evaluation of renewable energy and negative emissions options beyond biotic- and land-based methods are needed.

Atmospheric inversion of the surface CO2 flux with 13CO2 constraint

NASA Astrophysics Data System (ADS)

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

2013-10-01

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

Inverse modeling of CO2 sources and sinks using satellite observations of CO2 from TES and surface flask measurements

DOE Office of Scientific and Technical Information (OSTI.GOV)

Nassar, Ray; Jones, DBA; Kulawik, SS

2011-01-01

We infer CO2 surface fluxes using satellite observations of mid-tropospheric CO2 from the Tropospheric Emission Spectrometer (TES) and measurements of CO2 from surface flasks in a time-independent inversion analysis based on the GEOS-Chem model. Using TES CO2 observations over oceans, spanning 40 S 40 N, we find that the horizontal and vertical coverage of the TES and flask data are complementary. This complementarity is demonstrated by combining the datasets in a joint inversion, which provides better constraints than from either dataset alone, when a posteriori CO2 distributions are evaluated against independent ship and aircraft CO2 data. In particular, the jointmore » inversion offers improved constraints in the tropics where surface measurements are sparse, such as the tropical forests of South America. Aggregating the annual surface-to-atmosphere fluxes from the joint inversion for the year 2006 yields 1.13 0.21 PgC for the global ocean, 2.77 0.20 PgC for the global land biosphere and 3.90 0.29 PgC for the total global natural flux (defined as the sum of all biospheric, oceanic, and biomass burning contributions but excluding CO2 emissions from fossil fuel combustion). These global ocean and global land fluxes are shown to be near the median of the broad range of values from other inversion results for 2006. To achieve these results, a bias in TES CO2 in the Southern Hemisphere was assessed and corrected using aircraft flask data, and we demonstrate that our results have low sensitivity to variations in the bias correction approach. Overall, this analysis suggests that future carbon data assimilation systems can benefit by integrating in situ and satellite observations of CO2 and that the vertical information provided by satellite observations of mid-tropospheric CO2 combined with measurements of surface CO2, provides an important additional constraint for flux inversions.« less

Energy, chemical disequilibrium, and geological constraints on Europa.

PubMed

Hand, Kevin P; Carlson, Robert W; Chyba, Christopher F

2007-12-01

Europa is a prime target for astrobiology. The presence of a global subsurface liquid water ocean and a composition likely to contain a suite of biogenic elements make it a compelling world in the search for a second origin of life. Critical to these factors, however, may be the availability of energy for biological processes on Europa. We have examined the production and availability of oxidants and carbon-containing reductants on Europa to better understand the habitability of the subsurface ocean. Data from the Galileo Near-Infrared Mapping Spectrometer were used to constrain the surface abundance of CO(2) to 0.036% by number relative to water. Laboratory results indicate that radiolytically processed CO(2)-rich ices yield CO and H(2)CO(3); the reductants H(2)CO, CH(3)OH, and CH(4) are at most minor species. We analyzed chemical sources and sinks and concluded that the radiolytically processed surface of Europa could serve to maintain an oxidized ocean even if the surface oxidants (O(2), H(2)O(2), CO(2), SO(2), and SO(4) (2)) are delivered only once every approximately 0.5 Gyr. If delivery periods are comparable to the observed surface age (30-70 Myr), then Europa's ocean could reach O(2) concentrations comparable to those found in terrestrial surface waters, even if approximately 10(9) moles yr(1) of hydrothermally delivered reductants consume most of the oxidant flux. Such an ocean would be energetically hospitable for terrestrial marine macrofauna. The availability of reductants could be the limiting factor for biologically useful chemical energy on Europa.

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

NASA Astrophysics Data System (ADS)

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

2006-02-01

Decreased ventilation of the Southern Ocean in glacial time is implicated in most explanations of lower glacial atmospheric CO2. Today, the deep (>2000 m) ocean south of the Polar Front is rapidly ventilated from below, with the interaction of deep currents with topography driving high mixing rates well up into the water column. We show from a buoyancy budget that mixing rates are high in all the deep waters of the Southern Ocean. Between the surface and ~2000 m depth, water is upwelled by a residual meridional overturning that is directly linked to buoyancy fluxes through the ocean surface. Combined with the rapid deep mixing, this upwelling serves to return deep water to the surface on a short time scale. We propose two new mechanisms by which, in glacial time, the deep Southern Ocean may have been more isolated from the surface. Firstly, the deep ocean appears to have been more stratified because of denser bottom water resulting from intense sea ice formation near Antarctica. The greater stratification would have slowed the deep mixing. Secondly, subzero atmospheric temperatures may have meant that the present-day buoyancy flux from the atmosphere to the ocean surface was reduced or reversed. This in turn would have reduced or eliminated the upwelling (contrary to a common assumption, upwelling is not solely a function of the wind stress but is coupled to the air-sea buoyancy flux too). The observed very close link between Antarctic temperatures and atmospheric CO2 could then be explained as a natural consequence of the connection between the air-sea buoyancy flux and upwelling in the Southern Ocean, if slower ventilation of the Southern Ocean led to lower atmospheric CO2. Here we use a box model, similar to those of previous authors, to show that weaker mixing and reduced upwelling in the Southern Ocean can explain the low glacial atmospheric CO2 in such a formulation.

The Derivation Of A CO2 Fugacity Climatology From SOCAT's Global In SITU Data

NASA Astrophysics Data System (ADS)

Goddijn-Murphy, L. M.; Woolf, D. K.; Land, P. E.; Shutler, J. D.

2013-12-01

The Surface Ocean CO2 Atlas (SOCAT) has made millions of global underway sea surface measurements of CO2 publicly available, all in a uniform format and presented as fugacity, fCO2. However, these fCO2 values are valid strictly only for the instantaneous temperature at measurement and are not ideal for climatology. We recomputed these fCO2 values for the measurement month to be applicable to climatological sea surface temperatures, extrapolated to reference year 2010. The data were then spatially interpolated on a 1°×1° grid of the global oceans to produce 12 monthly fCO2 distributions. Our climatology data will be shared with the science community.

Surface Ocean pCO2 Seasonality and Sea-Air CO2 Flux Estimates for the North American East Coast

NASA Technical Reports Server (NTRS)

Signorini, Sergio; Mannino, Antonio; Najjar, Raymond G., Jr.; Friedrichs, Marjorie A. M.; Cai, Wei-Jun; Salisbury, Joe; Wang, Zhaohui Aleck; Thomas, Helmuth; Shadwick, Elizabeth

2013-01-01

Underway and in situ observations of surface ocean pCO2, combined with satellite data, were used to develop pCO2 regional algorithms to analyze the seasonal and interannual variability of surface ocean pCO2 and sea-air CO2 flux for five physically and biologically distinct regions of the eastern North American continental shelf: the South Atlantic Bight (SAB), the Mid-Atlantic Bight (MAB), the Gulf of Maine (GoM), Nantucket Shoals and Georges Bank (NS+GB), and the Scotian Shelf (SS). Temperature and dissolved inorganic carbon variability are the most influential factors driving the seasonality of pCO2. Estimates of the sea-air CO2 flux were derived from the available pCO2 data, as well as from the pCO2 reconstructed by the algorithm. Two different gas exchange parameterizations were used. The SS, GB+NS, MAB, and SAB regions are net sinks of atmospheric CO2 while the GoM is a weak source. The estimates vary depending on the use of surface ocean pCO2 from the data or algorithm, as well as with the use of the two different gas exchange parameterizations. Most of the regional estimates are in general agreement with previous studies when the range of uncertainty and interannual variability are taken into account. According to the algorithm, the average annual uptake of atmospheric CO2 by eastern North American continental shelf waters is found to be between 3.4 and 5.4 Tg C/yr (areal average of 0.7 to 1.0 mol CO2 /sq m/yr) over the period 2003-2010.

Ocean circulation and biogeochemistry moderate interannual and decadal surface water pH changes in the Sargasso Sea

USGS Publications Warehouse

Nathalie F. Goodkin,; Bo-Shian Wang,; Chen-Feng You,; Konrad Hughen,; Prouty, Nancy G.; Bates, Nicholas; Scott Doney,

2015-01-01

The oceans absorb anthropogenic CO2 from the atmosphere, lowering surface ocean pH, a concern for calcifying marine organisms. The impact of ocean acidification is challenging to predict as each species appears to respond differently and because our knowledge of natural changes to ocean pH is limited in both time and space. Here we reconstruct 222 years of biennial seawater pH variability in the Sargasso Sea from a brain coral, Diploria labyrinthiformis. Using hydrographic data from the Bermuda Atlantic Time-series Study and the coral-derived pH record, we are able to differentiate pH changes due to surface temperature versus those from ocean circulation and biogeochemical changes. We find that ocean pH does not simply reflect atmospheric CO2 trends but rather that circulation/biogeochemical changes account for >90% of pH variability in the Sargasso Sea and more variability in the last century than would be predicted from anthropogenic uptake of CO2 alone.

Autonomous observing platform CO2 data shed new light on the Southern Ocean carbon cycle

NASA Astrophysics Data System (ADS)

Olsen, Are

2017-06-01

While the number of surface ocean CO2 partial pressure (pCO2) measurements has soared the recent decades, the Southern Ocean remains undersampled. Williams et al. (2017, https://doi.org/10.1002/2016GB005541) now present pCO2 estimates based on data from pH-sensor equipped Bio-Argo floats, which have been measuring in the Southern Ocean since 2014. The authors demonstrate the utility of these data for understanding the carbon cycle in this region, which has a large influence on the distribution of CO2 between the ocean and atmosphere. Biogeochemical sensors deployed on autonomous platforms hold the potential to shape our view of the ocean carbon cycle in the coming decades.

Surface ocean carbon dioxide during the Atlantic Meridional Transect (1995-2013); evidence of ocean acidification

NASA Astrophysics Data System (ADS)

Kitidis, Vassilis; Brown, Ian; Hardman-Mountford, Nicholas; Lefèvre, Nathalie

2017-11-01

Here we present more than 21,000 observations of carbon dioxide fugacity in air and seawater (fCO2) along the Atlantic Meridional Transect (AMT) programme for the period 1995-2013. Our dataset consists of 11 southbound and 2 northbound cruises in boreal autumn and spring respectively. Our paper is primarily focused on change in the surface-ocean carbonate system during southbound cruises. We used observed fCO2 and total alkalinity (TA), derived from salinity and temperature, to estimate dissolved inorganic carbon (DIC) and pH (total scale). Using this approach, estimated pH was consistent with spectrophotometric measurements carried out on 3 of our cruises. The AMT cruises transect a range of biogeographic provinces where surface Chlorophyll-α spans two orders of magnitude (mesotrophic high latitudes to oligotrophic subtropical gyres). We found that surface Chlorophyll-α was negatively correlated with fCO2, but that the deep chlorophyll maximum was not a controlling variable for fCO2. Our data show clear evidence of ocean acidification across 100° of latitude in the Atlantic Ocean. Over the period 1995-2013 we estimated annual rates of change in: (a) sea surface temperature of 0.01 ± 0.05 °C, (b) seawater fCO2 of 1.44 ± 0.84 μatm, (c) DIC of 0.87 ± 1.02 μmol per kg and (d) pH of -0.0013 ± 0.0009 units. Monte Carlo simulations propagating the respective analytical uncertainties showed that the latter were < 5% of the observed trends. Seawater fCO2 increased at the same rate as atmospheric CO2.

Ocean Surface Carbon Dioxide Fugacity Observed from Space

NASA Technical Reports Server (NTRS)

Liu, W. Timothy; Xie, Xiaosu

2014-01-01

We have developed and validated a statistical model to estimate the fugacity (or partial pressure) of carbon dioxide (CO2) at sea surface (pCO2sea) from space-based observations of sea surface temperature (SST), chlorophyll, and salinity. More than a quarter million in situ measurements coincident with satellite data were compiled to train and validate the model. We have produced and made accessible 9 years (2002-2010) of the pCO2sea at 0.5 degree resolutions daily over the global ocean. The results help to identify uncertainties in current JPL Carbon Monitoring System (CMS) model-based and bottom-up estimates over the ocean. The utility of the data to reveal multi-year and regional variability of the fugacity in relation to prevalent oceanic parameters is demonstrated.

Evidence that global evapotranspiration makes a substantial contribution to the global atmospheric temperature slowdown

NASA Astrophysics Data System (ADS)

Leggett, L. Mark W.; Ball, David A.

2018-02-01

The difference between the time series trend for temperature expected from the increasing level of atmospheric CO2 and that for the (more slowly rising) observed temperature has been termed the global surface temperature slowdown. In this paper, we characterise the single time series made from the subtraction of these two time series as the `global surface temperature gap'. We also develop an analogous atmospheric CO2 gap series from the difference between the level of CO2 and first-difference CO2 (that is, the change in CO2 from one period to the next). This paper provides three further pieces of evidence concerning the global surface temperature slowdown. First, we find that the present size of both the global surface temperature gap and the CO2 gap is unprecedented over a period starting at least as far back as the 1860s. Second, ARDL and Granger causality analyses involving the global surface temperature gap against the major candidate physical drivers of the ocean heat sink and biosphere evapotranspiration are conducted. In each case where ocean heat data was available, it was significant in the models: however, evapotranspiration, or its argued surrogate precipitation, also remained significant in the models alongside ocean heat. In terms of relative scale, the standardised regression coefficient for evapotranspiration was repeatedly of the same order of magnitude as—typically as much as half that for—ocean heat. The foregoing is evidence that, alongside the ocean heat sink, evapotranspiration is also likely to be making a substantial contribution to the global atmospheric temperature outcome. Third, there is evidence that both the ocean heat sink and the evapotranspiration process might be able to continue into the future to keep the temperature lower than the level-of-CO2 models would suggest. It is shown that this means there can be benefit in using the first-difference CO2 to temperature relationship shown in Leggett and Ball (Atmos Chem Phys 15(20):11571-11592, 2015) to forecast future global surface temperature.

Deriving a sea surface climatology of CO2 fugacity in support of air-sea gas flux studies

NASA Astrophysics Data System (ADS)

Goddijn-Murphy, L. M.; Woolf, D. K.; Land, P. E.; Shutler, J. D.; Donlon, C.

2014-07-01

Climatologies, or long-term averages, of essential climate variables are useful for evaluating models and providing a baseline for studying anomalies. The Surface Ocean Carbon Dioxide (CO2) Atlas (SOCAT) has made millions of global underway sea surface measurements of CO2 publicly available, all in a uniform format and presented as fugacity, fCO2. fCO2 is highly sensitive to temperature and the measurements are only valid for the instantaneous sea surface temperature (SST) that is measured concurrent with the in-water CO2 measurement. To create a climatology of fCO2 data suitable for calculating air-sea CO2 fluxes it is therefore desirable to calculate fCO2 valid for climate quality SST. This paper presents a method for creating such a climatology. We recomputed SOCAT's fCO2 values for their respective measurement month and year using climate quality SST data from satellite Earth observation and then extrapolated the resulting fCO2 values to reference year 2010. The data were then spatially interpolated onto a 1° × 1° grid of the global oceans to produce 12 monthly fCO2 distributions for 2010. The partial pressure of CO2 (pCO2) is also provided for those who prefer to use pCO2. The CO2 concentration difference between ocean and atmosphere is the thermodynamic driving force of the air-sea CO2 flux, and hence the presented fCO2 distributions can be used in air-sea gas flux calculations together with climatologies of other climate variables.

Arctic Ocean CO2 uptake: an improved multiyear estimate of the air-sea CO2 flux incorporating chlorophyll a concentrations

NASA Astrophysics Data System (ADS)

Yasunaka, Sayaka; Siswanto, Eko; Olsen, Are; Hoppema, Mario; Watanabe, Eiji; Fransson, Agneta; Chierici, Melissa; Murata, Akihiko; Lauvset, Siv K.; Wanninkhof, Rik; Takahashi, Taro; Kosugi, Naohiro; Omar, Abdirahman M.; van Heuven, Steven; Mathis, Jeremy T.

2018-03-01

We estimated monthly air-sea CO2 fluxes in the Arctic Ocean and its adjacent seas north of 60° N from 1997 to 2014. This was done by mapping partial pressure of CO2 in the surface water (pCO2w) using a self-organizing map (SOM) technique incorporating chlorophyll a concentration (Chl a), sea surface temperature, sea surface salinity, sea ice concentration, atmospheric CO2 mixing ratio, and geographical position. We applied new algorithms for extracting Chl a from satellite remote sensing reflectance with close examination of uncertainty of the obtained Chl a values. The overall relationship between pCO2w and Chl a was negative, whereas the relationship varied among seasons and regions. The addition of Chl a as a parameter in the SOM process enabled us to improve the estimate of pCO2w, particularly via better representation of its decline in spring, which resulted from biologically mediated pCO2w reduction. As a result of the inclusion of Chl a, the uncertainty in the CO2 flux estimate was reduced, with a net annual Arctic Ocean CO2 uptake of 180 ± 130 Tg C yr-1. Seasonal to interannual variation in the CO2 influx was also calculated.

MEASUREMENTS OF PAST 14C LEVELS AND 13C/12C RATIOS IN THE SURFACE WATERS OF THE WORLD'S SUBPOLAR OCEANS.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Brown, T A

2010-04-22

Under this project we have developed methods that allow the reconstruction of past {sup 14}C levels of the surface waters of the subpolar North Pacific Ocean by measuring the {sup 14}C contents of archived salmon scales. The overall goal of this research was to reduce of the uncertainty in the uptake of fossil CO{sub 2} by the oceans and thereby improve the quantification of the global carbon cycle and to elucidate the fate of anthropogenic CO{sub 2}. Ocean General Circulation Models (OGCMs), with their three dimensional global spatial coverage and temporal modeling capabilities, provide the best route to accurately calculatingmore » the total uptake of CO{sub 2} by the oceans and, hence, to achieving the desired reduction in uncertainty. {sup 14}C has played, and continues to play, a central role in the validation of the OGCMs calculations, particularly with respect to those model components which govern the uptake of CO{sub 2} from the atmosphere and the transport of this carbon within the oceans. Under this project, we have developed time-series records of the {sup 14}C levels of the surface waters of three areas of the subpolar North Pacific Ocean. As the previously available data on the time-history of oceanic surface water {sup 14}C levels are very limited, these time-series records provide significant new {sup 14}C data to constrain and validate the OGCMs.« less

Estimating temporal and spatial variation of ocean surface pCO2 in the North Pacific using a Self Organizing Map neural network technique

NASA Astrophysics Data System (ADS)

Nakaoka, S.; Telszewski, M.; Nojiri, Y.; Yasunaka, S.; Miyazaki, C.; Mukai, H.; Usui, N.

2013-03-01

This study produced maps of the partial pressure of oceanic carbon dioxide (pCO2sea) in the North Pacific on a 0.25° latitude × 0.25° longitude grid from 2002 to 2008. The pCO2sea values were estimated by using a self-organizing map neural network technique to explain the non-linear relationships between observed pCO2sea data and four oceanic parameters: sea surface temperature (SST), mixed layer depth, chlorophyll a concentration, and sea surface salinity (SSS). The observed pCO2sea data was obtained from an extensive dataset generated by the volunteer observation ship program operated by the National Institute for Environmental Studies. The reconstructed pCO2sea values agreed rather well with the pCO2sea measurements, the root mean square error being 17.6 μatm. The pCO2sea estimates were improved by including SSS as one of the training parameters and by taking into account secular increases of pCO2sea that have tracked increases in atmospheric CO2. Estimated pCO2sea values accurately reproduced pCO2sea data at several stations in the North Pacific. The distributions of pCO2sea revealed by seven-year averaged monthly pCO2sea maps were similar to Lamont-Doherty Earth Observatory pCO2sea climatology and more precisely reflected oceanic conditions. The distributions of pCO2sea anomalies over the North Pacific during the winter clearly showed regional contrasts between El Niño and La Niña years related to changes of SST and vertical mixing.

Elevated pCO2 enhances bacterioplankton removal of organic carbon

PubMed Central

James, Anna K.; Passow, Uta; Brzezinski, Mark A.; Parsons, Rachel J.; Trapani, Jennifer N.; Carlson, Craig A.

2017-01-01

Factors that affect the removal of organic carbon by heterotrophic bacterioplankton can impact the rate and magnitude of organic carbon loss in the ocean through the conversion of a portion of consumed organic carbon to CO2. Through enhanced rates of consumption, surface bacterioplankton communities can also reduce the amount of dissolved organic carbon (DOC) available for export from the surface ocean. The present study investigated the direct effects of elevated pCO2 on bacterioplankton removal of several forms of DOC ranging from glucose to complex phytoplankton exudate and lysate, and naturally occurring DOC. Elevated pCO2 (1000–1500 ppm) enhanced both the rate and magnitude of organic carbon removal by bacterioplankton communities compared to low (pre-industrial and ambient) pCO2 (250 –~400 ppm). The increased removal was largely due to enhanced respiration, rather than enhanced production of bacterioplankton biomass. The results suggest that elevated pCO2 can increase DOC consumption and decrease bacterioplankton growth efficiency, ultimately decreasing the amount of DOC available for vertical export and increasing the production of CO2 in the surface ocean. PMID:28257422

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

USGS Publications Warehouse

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

2016-01-01

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

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

NASA Astrophysics Data System (ADS)

Bakker, D. C. E.; Pfeil, B.; Smith, K.; Hankin, S.; Olsen, A.; Alin, S. R.; Cosca, C.; Harasawa, S.; Kozyr, A.; Nojiri, Y.; O'Brien, K. M.; Schuster, U.; Telszewski, M.; Tilbrook, B.; Wada, C.; Akl, J.; Barbero, L.; Bates, N. R.; Boutin, J.; Bozec, Y.; Cai, W.-J.; Castle, R. D.; Chavez, F. P.; Chen, L.; Chierici, M.; Currie, K.; de Baar, H. J. W.; Evans, W.; Feely, R. A.; Fransson, A.; Gao, Z.; Hales, B.; Hardman-Mountford, N. J.; Hoppema, M.; Huang, W.-J.; Hunt, C. W.; Huss, B.; Ichikawa, T.; Johannessen, T.; Jones, E. M.; Jones, S. D.; Jutterström, S.; Kitidis, V.; Körtzinger, A.; Landschützer, P.; Lauvset, S. K.; Lefèvre, N.; Manke, A. B.; Mathis, J. T.; Merlivat, L.; Metzl, N.; Murata, A.; Newberger, T.; Omar, A. M.; Ono, T.; Park, G.-H.; Paterson, K.; Pierrot, D.; Ríos, A. F.; Sabine, C. L.; Saito, S.; Salisbury, J.; Sarma, V. V. S. S.; Schlitzer, R.; Sieger, R.; Skjelvan, I.; Steinhoff, T.; Sullivan, K. F.; Sun, H.; Sutton, A. J.; Suzuki, T.; Sweeney, C.; Takahashi, T.; Tjiputra, J.; Tsurushima, N.; van Heuven, S. M. A. C.; Vandemark, D.; Vlahos, P.; Wallace, D. W. R.; Wanninkhof, R.; Watson, A. J.

2014-03-01

The Surface Ocean CO2 Atlas (SOCAT), an activity of the international marine carbon research community, provides access to synthesis and gridded fCO2 (fugacity of carbon dioxide) products for the surface oceans. Version 2 of SOCAT is an update of the previous release (version 1) with more data (increased from 6.3 million to 10.1 million surface water fCO2 values) and extended data coverage (from 1968-2007 to 1968-2011). The quality control criteria, while identical in both versions, have been applied more strictly in version 2 than in version 1. The SOCAT website (http://www.socat.info/) has links to quality control comments, metadata, individual data set files, and synthesis and gridded data products. Interactive online tools allow visitors to explore the richness of the data. Applications of SOCAT include process studies, quantification of the ocean carbon sink and its spatial, seasonal, year-to-year and longerterm variation, as well as initialisation or validation of ocean carbon models and coupled climate-carbon models. Data coverage Repository-References: Individual data set files and synthesis product: doi:10.1594/PANGAEA.811776 Gridded products: doi:10.3334/CDIAC/OTG.SOCAT_V2_GRID Available at: http://www.socat.info/ Coverage: 79° S to 90° N; 180° W to 180° E Location Name: Global Oceans and Coastal Seas Date/Time Start: 16 November 1968 ate/Time End: 26 December 2011

Technical Report Series on Global Modeling and Data Assimilation. Volume 31; Global Surface Ocean Carbon Estimates in a Model Forced by MERRA

NASA Technical Reports Server (NTRS)

Gregg, Watson W.; Casey, Nancy W.; Rousseaux, Cecile S.

2013-01-01

MERRA products were used to force an established ocean biogeochemical model to estimate surface carbon inventories and fluxes in the global oceans. The results were compared to public archives of in situ carbon data and estimates. The model exhibited skill for ocean dissolved inorganic carbon (DIC), partial pressure of ocean CO2 (pCO2) and air-sea fluxes (FCO2). The MERRA-forced model produced global mean differences of 0.02% (approximately 0.3 microns) for DIC, -0.3% (about -1.2 (micro) atm; model lower) for pCO2, and -2.3% (-0.003 mol C/sq m/y) for FCO2 compared to in situ estimates. Basin-scale distributions were significantly correlated with observations for all three variables (r=0.97, 0.76, and 0.73, P<0.05, respectively for DIC, pCO2, and FCO2). All major oceanographic basins were represented as sources to the atmosphere or sinks in agreement with in situ estimates. However, there were substantial basin-scale and local departures.

Kinetic bottlenecks to chemical exchange rates for deep-sea animals - Part 2: Carbon Dioxide

NASA Astrophysics Data System (ADS)

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

2013-04-01

Increased 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. Discussion of these impacts has so far focused only on changes in the oceanic bulk fluid properties (ΔpH, Δ[∑ CO2], etc.) as the critical variable and with a major focus on carbonate shell formation. Here we describe the rate problem for animals that must export CO2 at about the same rate at which O2 is consumed. We analyse the basic properties controlling CO2 export within the diffusive boundary layer around marine animals in an ocean changing in temperature (T) and CO2 concentration 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 with CO2 the influence of the seawater carbonate acid-base system needs to be considered. These reactions significantly facilitate CO2 efflux compared to O2 intake at equal temperature, pressure and fluid flow rate under typical oceanic concentrations. The effect of these reactions can be described by an enhancement factor, similar to that widely used for CO2 invasion at the sea surface. While organisms do need to actively regulate flow over their surface to thin the boundary layer to take up enough O2, this seems to be not necessary to facilitate CO2 efflux. Instead, the main impacts of rising oceanic CO2 will most likely be those associated with classical ocean acidification science. Regionally, as with O2, the combination of T, P and pH/pCO2 creates a zone of maximum CO2 stress at around 1000 m depth.

Mapping of the air-sea CO2 flux in the Arctic Ocean and its adjacent seas: Basin-wide distribution and seasonal to interannual variability

NASA Astrophysics Data System (ADS)

Yasunaka, Sayaka; Murata, Akihiko; Watanabe, Eiji; Chierici, Melissa; Fransson, Agneta; van Heuven, Steven; Hoppema, Mario; Ishii, Masao; Johannessen, Truls; Kosugi, Naohiro; Lauvset, Siv K.; Mathis, Jeremy T.; Nishino, Shigeto; Omar, Abdirahman M.; Olsen, Are; Sasano, Daisuke; Takahashi, Taro; Wanninkhof, Rik

2016-09-01

We produced 204 monthly maps of the air-sea CO2 flux in the Arctic north of 60°N, including the Arctic Ocean and its adjacent seas, from January 1997 to December 2013 by using a self-organizing map technique. The partial pressure of CO2 (pCO2) in surface water data were obtained by shipboard underway measurements or calculated from alkalinity and total inorganic carbon of surface water samples. Subsequently, we investigated the basin-wide distribution and seasonal to interannual variability of the CO2 fluxes. The 17-year annual mean CO2 flux shows that all areas of the Arctic Ocean and its adjacent seas were net CO2 sinks. The estimated annual CO2 uptake by the Arctic Ocean was 180 TgC yr-1. The CO2 influx was strongest in winter in the Greenland/Norwegian Seas (>15 mmol m-2 day-1) and the Barents Sea (>12 mmol m-2 day-1) because of strong winds, and strongest in summer in the Chukchi Sea (∼10 mmol m-2 day-1) because of the sea-ice retreat. In recent years, the CO2 uptake has increased in the Greenland/Norwegian Sea and decreased in the southern Barents Sea, owing to increased and decreased air-sea pCO2 differences, respectively.

Could artificial ocean alkalinization protect tropical coral ecosystems from ocean acidification?

NASA Astrophysics Data System (ADS)

Feng, Ellias Y.; Keller, David P.; Koeve, Wolfgang; Oschlies, Andreas

2016-07-01

Artificial ocean alkalinization (AOA) is investigated as a method to mitigate local ocean acidification and protect tropical coral ecosystems during a 21st century high CO2 emission scenario. Employing an Earth system model of intermediate complexity, our implementation of AOA in the Great Barrier Reef, Caribbean Sea and South China Sea regions, shows that alkalinization has the potential to counteract expected 21st century local acidification in regard to both oceanic surface aragonite saturation Ω and surface pCO2. Beyond preventing local acidification, regional AOA, however, results in locally elevated aragonite oversaturation and pCO2 decline. A notable consequence of stopping regional AOA is a rapid shift back to the acidified conditions of the target regions. We conclude that AOA may be a method that could help to keep regional coral ecosystems within saturation states and pCO2 values close to present-day values even in a high-emission scenario and thereby might ‘buy some time’ against the ocean acidification threat, even though regional AOA does not significantly mitigate the warming threat.

Global sea-air CO 2 flux based on climatological surface ocean pCO 2, and seasonal biological and temperature effects

NASA Astrophysics Data System (ADS)

Takahashi, Taro; Sutherland, Stewart C.; Sweeney, Colm; Poisson, Alain; Metzl, Nicolas; Tilbrook, Bronte; Bates, Nicolas; Wanninkhof, Rik; Feely, Richard A.; Sabine, Christopher; Olafsson, Jon; Nojiri, Yukihiro

Based on about 940,000 measurements of surface-water pCO 2 obtained since the International Geophysical Year of 1956-59, the climatological, monthly distribution of pCO 2 in the global surface waters representing mean non-El Niño conditions has been obtained with a spatial resolution of 4°×5° for a reference year 1995. The monthly and annual net sea-air CO 2 flux has been computed using the NCEP/NCAR 41-year mean monthly wind speeds. An annual net uptake flux of CO 2 by the global oceans has been estimated to be 2.2 (+22% or -19%) Pg C yr -1 using the (wind speed) 2 dependence of the CO 2 gas transfer velocity of Wanninkhof (J. Geophys. Res. 97 (1992) 7373). The errors associated with the wind-speed variation have been estimated using one standard deviation (about±2 m s -1) from the mean monthly wind speed observed over each 4°×5° pixel area of the global oceans. The new global uptake flux obtained with the Wanninkhof (wind speed) 2 dependence is compared with those obtained previously using a smaller number of measurements, about 250,000 and 550,000, respectively, and are found to be consistent within±0.2 Pg C yr -1. This estimate for the global ocean uptake flux is consistent with the values of 2.0±0.6 Pg C yr -1 estimated on the basis of the observed changes in the atmospheric CO 2 and oxygen concentrations during the 1990s (Nature 381 (1996) 218; Science 287 (2000) 2467). However, if the (wind speed) 3 dependence of Wanninkhof and McGillis (Res. Lett. 26 (1999) 1889) is used instead, the annual ocean uptake as well as the sensitivity to wind-speed variability is increased by about 70%. A zone between 40° and 60° latitudes in both the northern and southern hemispheres is found to be a major sink for atmospheric CO 2. In these areas, poleward-flowing warm waters meet and mix with the cold subpolar waters rich in nutrients. The pCO 2 in the surface water is decreased by the cooling effect on warm waters and by the biological drawdown of pCO 2 in subpolar waters. High wind speeds over these low pCO 2 waters increase the CO 2 uptake rate by the ocean waters. The pCO 2 in surface waters of the global oceans varies seasonally over a wide range of about 60% above and below the current atmospheric pCO 2 level of about 360 μatm. A global map showing the seasonal amplitude of surface-water pCO 2 is presented. The effect of biological utilization of CO 2 is differentiated from that of seasonal temperature changes using seasonal temperature data. The seasonal amplitude of surface-water pCO 2 in high-latitude waters located poleward of about 40° latitude and in the equatorial zone is dominated by the biology effect, whereas that in the temperate gyre regions is dominated by the temperature effect. These effects are about 6 months out of phase. Accordingly, along the boundaries between these two regimes, they tend to cancel each other, forming a zone of small pCO 2 amplitude. In the oligotrophic waters of the northern and southern temperate gyres, the biology effect is about 35 μatm on average. This is consistent with the biological export flux estimated by Laws et al. (Glob. Biogeochem. Cycles 14 (2000) 1231). Small areas such as the northwestern Arabian Sea and the eastern equatorial Pacific, where seasonal upwelling occurs, exhibit intense seasonal changes in pCO 2 due to the biological drawdown of CO 2.

Southern Ocean carbon-wind stress feedback

NASA Astrophysics Data System (ADS)

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

2018-02-01

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

Earth 2075 (CO2) - can Ocean-Amplified Carbon Capture (oacc) Impart Atmospheric CO2-SINKING Ability to CCS Fossil Energy?

NASA Astrophysics Data System (ADS)

Fry, R.; Routh, M.; Chaudhuri, S.; Fry, S.; Ison, M.; Hughes, S.; Komor, C.; Klabunde, K.; Sethi, V.; Collins, D.; Polkinghorn, W.; Wroobel, B.; Hughes, J.; Gower, G.; Shkolnik, J.

2017-12-01

Previous attempts to capture atmospheric CO2 by algal blooming were stalled by ocean viruses, zooplankton feeding, and/or bacterial decomposition of surface blooms, re-releasing captured CO2 instead of exporting it to seafloor. CCS fossil energy coupling could bypass algal bloom limits—enabling capture of 10 GtC/yr atmospheric CO2 by selective emiliania huxleyi (EHUX) blooming in mid-latitude open oceans, far from coastal waters and polar seas. This could enable a 500 GtC drawdown, 350 ppm restoration by 2050, 280 ppm CO2 by 2075, and ocean pH 8.2. White EHUX blooms could also reflect sunlight back into outer space and seed extra ocean cloud cover, via DMS release, to raise albedo 1.8%—restoring preindustrial temperature (ΔT = 0°C) by 2030. Open oceans would avoid post-bloom anoxia, exclusively a coastal water phenomenon. The EHUX calcification reaction initially sources CO2, but net sinking prevails in follow-up equilibration reactions. Heavier-than-water EHUX sink captured CO2 to the sea floor before surface decomposition occurs. Seeding EHUX high on their nonlinear growth curve could accelerate short-cycle secondary open-ocean blooming—overwhelming mid-latitude viruses, zooplankton, and competition from other algae. Mid-latitude "ocean deserts" exhibit low viral, zooplankton, and bacterial counts. Thermocline prevents nutrient upwelling that would otherwise promote competing algae. Adding nitrogen nutrient would foster exclusive EHUX blooming. Elevated EHUX seed levels could arise from sealed, pH-buffered, floating, seed-production bioreactors infused with 10% CO2 from carbon feedstock supplied by inland CCS fossil power plants capturing 90% of emissions as liquid CO2. Deep-water SPAR platforms extract natural gas from beneath the sea floor. On-platform Haber and pH processing could convert extracted CH4 to buffered NH4+ nutrient, enabling ≥0.7 GtC/yr of bioreactor seed production and 10 GtC/yr of amplified secondary open-ocean CO2 capture—making CCS fossil energy 1400% carbon negative.

Buffered versus non-buffered ocean carbon reservoir variations: Application to the sensitivity of atmospheric pCO2 to ocean circulation changes

NASA Astrophysics Data System (ADS)

d'Orgeville, M.; England, M. H.; Sijp, W. P.

2011-12-01

Changes in the ocean circulation on millenial timescales can impact the atmospheric CO2 concentration by two distinct mechanisms: either by modifying the non-buffered ocean carbon storage (through changes in the physical and biological oceanic pumps) or by directly varying the surface mean oceanic partial pressure of pCO2 (through changes in mean surface alkalinity, temperature or salinity). The equal importance of the two mechanisms is illustrated here by introducing a diagnostic buffered carbon budget on the results of simulations performed with an Earth System Climate Model. For all the circulation changes considered in this study (due to a freshening of the North Atlantic, or a change in the Southern Hemisphere Westerly winds), the sign of the atmospheric CO2 response is opposite to the sign of the non-buffered ocean carbon storage change, indicating a transfer of carbon between ocean and atmosphere reservoirs. However the concomitant changes in the buffered ocean carbon reservoir can either greatly enhance or almost inhibit the atmospheric response depending on its sign. This study also demonstrates the utility of the buffered carbon budget approach in diagnosing the transient response of the global carbon cycle to climatic variations.

Linking water and carbon cycles through salinity observed from space

NASA Astrophysics Data System (ADS)

Xie, X.; Liu, W. T.

2017-12-01

The association of ocean surface salinity in global hydrological cycle and climate change has been traditionally studied through the examination of its tendency and advection as manifestation of ocean's heat and water fluxes with the atmosphere. The variability of surface heat and water fluxes are linked to top of atmosphere radiation, whose imbalance is the main cause of global warming. Besides the link of salinity to greenhouse warming through water balance, this study will focus on the effect of changing salinity on carbon dioxide flux between the ocean and the atmosphere. We have built statistical models to estimate the partial pressure of carbon dioxide (pCO2) and ocean acidification (in terms of total alkalinity and pH) using spacebased data. PCO2 is a critical parameter governing ocean as source and sink of the accumulated greenhouse gas in the atmosphere. The exchange also causes ocean acidification, which is detrimental to marine lives and ecology. Before we had sufficient spacebased salinity measurements coincident with in situ pCO2 measurement, we trained our statistical models to use satellite sea surface temperature and chlorophyll, with one model using salinity climatology and the other without. We found significant differences between the two models in regions of strong water input through river discharge and surface water flux. The pCO2 output follows the seasonal salinity advection of the Amazon outflow. The seasonal salinity advection between Bay of Bengal and Arabian Sea are followed by change of pCO2 and total alkalinity. At shorter time scales, the signatures of rain associated with intraseasonal organized convection of summer monsoon can be detected. We have observed distribution agreement of among pCO2, surface salinity, and surface water flux for variation from a few days to a few years under the Pacific ITCZ; the agreement varies slightly with season and longitudes and the reason is under study.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Observational constraints on the global atmospheric CO2 budget

NASA Technical Reports Server (NTRS)

Tans, Pieter P.; Fung, Inez Y.; Takahashi, Taro

1990-01-01

Observed atmospheric concentrations of CO2 and data on the partial pressures of CO2 in surface ocean waters are combined to identify globally significant sources and sinks of CO2. The atmospheric data are compared with boundary layer concentrations calculated with the transport fields generated by a general circulation model (GCM) for specified source-sink distributions. In the model the observed north-south atmospheric concentration gradient can be maintained only if sinks for CO2 are greater in the Northern than in the Southern Hemisphere. The observed differences between the partial pressure of CO2 in the surface waters of the Northern Hemisphere and the atmosphere are too small for the oceans to be the major sink of fossil fuel CO2. Therefore, a large amount of the CO2 is apparently absorbed on the continents by terrestrial ecosystems.

The relationship between delta C-13 of organic matter and (CO2(aq)) in ocean surface water - Data from the JGOFS site in the northeast Atlantic Ocean and a model. [Joint Global Ocean Flux Study

NASA Technical Reports Server (NTRS)

Rau, G. H.; Takahashi, T.; Des Marais, D. J.; Repeta, D. J.; Martin, J. H.

1992-01-01

Consistent with the hypothesis that plankton delta C-14 and (CO2(aq)) are inversely related, increases in both sinking and suspended particulate organic matter (POM) delta C-13 detected by the Joint Global Ocean Flux Study (JGOFS) were highly negatively correlated with mixed-layer (CO2(aq)). A model of plant delta C-13 by Farquhar et al. (1982) is adapted to show that under a constant phytoplankton demand for CO2 an inverse nonlinear suspended POM delta C-13 response to ambient (CO2(aq)) is expected. Differences between predicted and observed suspended POM delta C-13 vs. (CO2(aq)) trends and among observed relationships can be reconciled if biological CO2 demand is allowed to vary.

Sensitivity of ocean acidification and oxygen to the uncertainty in climate change

NASA Astrophysics Data System (ADS)

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

2014-05-01

Due to increasing atmospheric CO2 concentrations and associated climate change, the global ocean is undergoing substantial physical and biogeochemical changes. Among these, changes in ocean oxygen and carbonate chemistry have great implication for marine biota. There is considerable uncertainty in the projections of future climate change, and it is unclear how the uncertainty in climate change would also affect the projection of oxygen and carbonate chemistry. To investigate this issue, we use an Earth system model of intermediate complexity to perform a set of simulations, including that which involves no radiative effect of atmospheric CO2 and those which involve CO2-induced climate change with climate sensitivity varying from 0.5 °C to 4.5 °C. Atmospheric CO2 concentration is prescribed to follow RCP 8.5 pathway and its extensions. Climate change affects carbonate chemistry and oxygen mainly through its impact on ocean temperature, ocean ventilation, and concentration of dissolved inorganic carbon and alkalinity. It is found that climate change mitigates the decrease of carbonate ions at the ocean surface but has negligible effect on surface ocean pH. Averaged over the whole ocean, climate change acts to decrease oxygen concentration but mitigates the CO2-induced reduction of carbonate ion and pH. In our simulations, by year 2500, every degree increase of climate sensitivity warms the ocean by 0.8 °C and reduces ocean-mean dissolved oxygen concentration by 5.0%. Meanwhile, every degree increase of climate sensitivity buffers CO2-induced reduction in ocean-mean carbonate ion concentration and pH by 3.4% and 0.02 units, respectively. Our study demonstrates different sensitivities of ocean temperature, carbonate chemistry, and oxygen, in terms of both the sign and magnitude to the amount of climate change, which have great implications for understanding the response of ocean biota to climate change.

Determination of the Prebomb Southern (Antartic) Ocean Radiocarbon in Organic Matter

DOE Office of Scientific and Technical Information (OSTI.GOV)

Guilderson, T P

2001-02-26

The Southern Hemisphere is an important and unique region of the world's oceans for water-mass formation and mixing, upwelling, nutrient utilization, and carbon export. In fact, one of the primary interests of the oceanographic community is to decipher the climatic record of these processes in the source or sink terms for Southern Ocean surface waters in the CO{sub 2} balance of the atmosphere. Current coupled ocean-atmosphere modeling efforts to trace the input of CO{sub 2} into the ocean imply a strong sink of anthropogenic CO{sub 2} in the southern ocean. However, because of its relative inaccessibility and the difficulty inmore » directly measuring CO{sub 2} fluxes in the Southern Ocean, these results are controversial at best. An accepted diagnostic of the exchange of CO{sub 2} between the atmosphere and ocean is the prebomb distribution of radiocarbon in the ocean and its time-history since atmospheric nuclear testing. Such histories of {sup 14}C in the surface waters of the Southern Ocean do not currently exist, primarily because there are few continuous biological archives (e.g., in corals) such as those that have been used to monitor the {sup 14}C history of the tropics and subtropics. One of the possible long-term archives is the scallop Adamussium collbecki. Although not independently confirmed, relatively crude growth rate estimates of A. collbecki indicate that it has the potential to provide continuous 100 year time-series. We are exploring the suitability of this potential archive.« less

Coccolithophore surface distributions in the North Atlantic and their modulation of the air-sea flux of CO2 from 10 years of satellite Earth observation data

NASA Astrophysics Data System (ADS)

Shutler, J. D.; Land, P. E.; Brown, C. W.; Findlay, H. S.; Donlon, C. J.; Medland, M.; Snooke, R.; Blackford, J. C.

2013-04-01

Coccolithophores are the primary oceanic phytoplankton responsible for the production of calcium carbonate (CaCO3). These climatically important plankton play a key role in the oceanic carbon cycle as a major contributor of carbon to the open ocean carbonate pump (~50%) and their calcification can affect the atmosphere-to-ocean (air-sea) uptake of carbon dioxide (CO2) through increasing the seawater partial pressure of CO2 (pCO2). Here we document variations in the areal extent of surface blooms of the globally important coccolithophore, Emiliania huxleyi, in the North Atlantic over a 10-year period (1998-2007), using Earth observation data from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS). We calculate the annual mean sea surface areal coverage of E. huxleyi in the North Atlantic to be 474 000 ± 104 000 km2, which results in a net CaCO3 carbon (CaCO3-C) production of 0.14-1.71 Tg CaCO3-C per year. However, this surface coverage (and, thus, net production) can fluctuate inter-annually by -54/+8% about the mean value and is strongly correlated with the El Niño/Southern Oscillation (ENSO) climate oscillation index (r=0.75, p<0.02). Our analysis evaluates the spatial extent over which the E. huxleyi blooms in the North Atlantic can increase the pCO2 and, thus, decrease the localised air-sea flux of atmospheric CO2. In regions where the blooms are prevalent, the average reduction in the monthly air-sea CO2 flux can reach 55%. The maximum reduction of the monthly air-sea CO2 flux in the time series is 155%. This work suggests that the high variability, frequency and distribution of these calcifying plankton and their impact on pCO2 should be considered if we are to fully understand the variability of the North Atlantic air-to-sea flux of CO2. We estimate that these blooms can reduce the annual N. Atlantic net sink atmospheric CO2 by between 3-28%.

Impact of anthropogenic atmospheric nitrogen and sulfur deposition on ocean acidification and the inorganic carbon system.

PubMed

Doney, Scott C; Mahowald, Natalie; Lima, Ivan; Feely, Richard A; Mackenzie, Fred T; Lamarque, Jean-Francois; Rasch, Phil J

2007-09-11

Fossil fuel combustion and agriculture result in atmospheric deposition of 0.8 Tmol/yr reactive sulfur and 2.7 Tmol/yr nitrogen to the coastal and open ocean near major source regions in North America, Europe, and South and East Asia. Atmospheric inputs of dissociation products of strong acids (HNO(3) and H2SO(4)) and bases (NH(3)) alter surface seawater alkalinity, pH, and inorganic carbon storage. We quantify the biogeochemical impacts by using atmosphere and ocean models. The direct acid/base flux to the ocean is predominately acidic (reducing total alkalinity) in the temperate Northern Hemisphere and alkaline in the tropics because of ammonia inputs. However, because most of the excess ammonia is nitrified to nitrate (NO(3)(-)) in the upper ocean, the effective net atmospheric input is acidic almost everywhere. The decrease in surface alkalinity drives a net air-sea efflux of CO(2), reducing surface dissolved inorganic carbon (DIC); the alkalinity and DIC changes mostly offset each other, and the decline in surface pH is small. Additional impacts arise from nitrogen fertilization, leading to elevated primary production and biological DIC drawdown that reverses in some places the sign of the surface pH and air-sea CO(2) flux perturbations. On a global scale, the alterations in surface water chemistry from anthropogenic nitrogen and sulfur deposition are a few percent of the acidification and DIC increases due to the oceanic uptake of anthropogenic CO(2). However, the impacts are more substantial in coastal waters, where the ecosystem responses to ocean acidification could have the most severe implications for mankind.

The Southern Ocean as a constraint to reduce uncertainty in future ocean carbon sinks

DOE PAGES

Kessler, A.; Tjiputra, J.

2016-04-07

Earth system model (ESM) simulations exhibit large biases compares to observation-based estimates of the present ocean CO 2 sink. The inter-model spread in projections increases nearly 2-fold by the end of the 21st century and therefore contributes significantly to the uncertainty of future climate projections. In this study, the Southern Ocean (SO) is shown to be one of the hot-spot regions for future uptake of anthropogenic CO 2, characterized by both the solubility pump and biologically mediated carbon drawdown in the spring and summer. Here, we show, by analyzing a suite of fully interactive ESMs simulations from the Coupled Model Intercomparisonmore » Project phase 5 (CMIP5) over the 21st century under the high-CO 2 Representative Concentration Pathway (RCP) 8.5 scenario, that the SO is the only region where the atmospheric CO 2 uptake rate continues to increase toward the end of the 21st century. Furthermore, our study discovers a strong inter-model link between the contemporary CO 2 uptake in the Southern Ocean and the projected global cumulated uptake over the 21st century. This strong correlation suggests that models with low (high) carbon uptake rate in the contemporary SO tend to simulate low (high) uptake rate in the future. None the less, our analysis also shows that none of the models fully capture the observed biophysical mechanisms governing the CO 2 fluxes in the SO. The inter-model spread for the contemporary CO 2 uptake in the Southern Ocean is attributed to the variations in the simulated seasonal cycle of surface pCO 2. Two groups of model behavior have been identified. The first one simulates anomalously strong SO carbon uptake, generally due to both too strong a net primary production and too low a surface pCO 2 in December–January. The second group simulates an opposite CO 2 flux seasonal phase, which is driven mainly by the bias in the sea surface temperature variability. Furthermore, we show that these biases are persistent throughout the 21st century, which highlights the urgent need for a sustained and comprehensive biogeochemical monitoring system in the Southern Ocean to better constrain key processes represented in current model systems.« less

The Southern Ocean as a constraint to reduce uncertainty in future ocean carbon sinks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kessler, A.; Tjiputra, J.

Earth system model (ESM) simulations exhibit large biases compares to observation-based estimates of the present ocean CO 2 sink. The inter-model spread in projections increases nearly 2-fold by the end of the 21st century and therefore contributes significantly to the uncertainty of future climate projections. In this study, the Southern Ocean (SO) is shown to be one of the hot-spot regions for future uptake of anthropogenic CO 2, characterized by both the solubility pump and biologically mediated carbon drawdown in the spring and summer. Here, we show, by analyzing a suite of fully interactive ESMs simulations from the Coupled Model Intercomparisonmore » Project phase 5 (CMIP5) over the 21st century under the high-CO 2 Representative Concentration Pathway (RCP) 8.5 scenario, that the SO is the only region where the atmospheric CO 2 uptake rate continues to increase toward the end of the 21st century. Furthermore, our study discovers a strong inter-model link between the contemporary CO 2 uptake in the Southern Ocean and the projected global cumulated uptake over the 21st century. This strong correlation suggests that models with low (high) carbon uptake rate in the contemporary SO tend to simulate low (high) uptake rate in the future. None the less, our analysis also shows that none of the models fully capture the observed biophysical mechanisms governing the CO 2 fluxes in the SO. The inter-model spread for the contemporary CO 2 uptake in the Southern Ocean is attributed to the variations in the simulated seasonal cycle of surface pCO 2. Two groups of model behavior have been identified. The first one simulates anomalously strong SO carbon uptake, generally due to both too strong a net primary production and too low a surface pCO 2 in December–January. The second group simulates an opposite CO 2 flux seasonal phase, which is driven mainly by the bias in the sea surface temperature variability. Furthermore, we show that these biases are persistent throughout the 21st century, which highlights the urgent need for a sustained and comprehensive biogeochemical monitoring system in the Southern Ocean to better constrain key processes represented in current model systems.« less

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

PubMed

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

2017-11-30

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

Decadal predictions of the North Atlantic CO2 uptake.

PubMed

Li, Hongmei; Ilyina, Tatiana; Müller, Wolfgang A; Sienz, Frank

2016-03-30

As a major CO2 sink, the North Atlantic, especially its subpolar gyre region, is essential for the global carbon cycle. Decadal fluctuations of CO2 uptake in the North Atlantic subpolar gyre region are associated with the evolution of the North Atlantic Oscillation, the Atlantic meridional overturning circulation, ocean mixing and sea surface temperature anomalies. While variations in the physical state of the ocean can be predicted several years in advance by initialization of Earth system models, predictability of CO2 uptake has remained unexplored. Here we investigate the predictability of CO2 uptake variations by initialization of the MPI-ESM decadal prediction system. We find large multi-year variability in oceanic CO2 uptake and demonstrate that its potential predictive skill in the western subpolar gyre region is up to 4-7 years. The predictive skill is mainly maintained in winter and is attributed to the improved physical state of the ocean.

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

NASA Astrophysics Data System (ADS)

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

2012-12-01

Atmospheric carbon dioxide (pCO2) induced ocean acidification and rising seawater temperatures are identified as two of the greatest threats to modern coral reefs. Within this century, surface seawater pH is expected to decrease by at least 0.3 units, and sea surface temperature is predicted to rise by 1 to 3 °C. However, uncertainty remains as to whether ocean acidification or ocean warming will have a more deleterious impact on coral reefs by the end of the century. Here, we present results of 95-day laboratory experiments in which we investigated the impact of CO2-induced ocean acidification and temperature on the calcification rate of the tropical reef-building zooxanthellate scleractinian coral Siderastrea siderea. We found that calcification rates for S. siderea, estimated from buoyant weighing, increased as pCO2 increased from a pre-industrial value of 324 ppm to a near-present-day value of 477 ppm, remained unchanged as pCO2 increased from 477 ppm to the predicted end-of-century value of 604 ppm, and only declined at 6-times the modern pCO2 value of 2553 ppm. Corals reared at average pCO2 of 488 ppm and at temperatures of 25 and 32 °C, approximately the lower and upper temperature extremes for this species, calcified at lower rates relative to corals reared at 28 °C under equivalent pCO2. These results support the existing evidence that scleractinian corals such as S. siderea are able to manipulate the carbonate chemistry at their calcification site, enabling them to maintain their calcification rates under elevated pCO2 levels predicted for the end of this century. However, exposure of S. siderea corals to sea surface temperatures predicted for tropical waters for the end of this century grossly impaired their rate of calcification. These findings suggest that ocean warming poses a more immediate threat to the coral S. siderea than does ocean acidification, at least under scenarios (B1, A1T, and B2) predicted by the Intergovernmental Panel on Climate Change for the end of the 21st century. We are presently investigating the calcification responses of S. siderea to the combined effects of ocean acidification and warming, in order to better constrain how corals will respond to global CO2-induced changes that are predicted for the near future.

Response to CO2 Transient Increase in the GISS Coupled Model: Regional Coolings in a Warming Climate

NASA Technical Reports Server (NTRS)

Russell, Gary L.; Rind, David

1999-01-01

The (GISS) Goddard Institute for Space Studies coupled atmosphere-ocean model is used to investigate the effect of increased atmospheric CO2 by comparing a compounded 1 percent CO2 increase experiment with a control simulation. After 70 years of integration, the global surface air temperature in the 1 percent CO2 experiment is 1.43 C warmer. In spite of this global warming, there are two distinct regions, the northern Atlantic Ocean and the southern Pacific Ocean, where the surface air temperature is up to 4 C cooler. This situation is maintained by two positive feedbacks: a local effect on convection in the South Pacific and a non-local impact on the meridional circulation in the North Atlantic. The poleward transport of latent energy and dry static energy by the atmosphere is greater in the 1 percent CO2 experiment, caused by warming and therefore increased water vapor and greater greenhouse capacity at lower latitudes. The larger atmospheric transports tend to reduce upward vertical fluxes of heat and moisture from the ocean surface at high latitudes, which has the effect of stabilizing the ocean, reducing both convection and the thermohaline circulation. With less convection, less warm water is brought up from below, and with a reduced North Atlantic thermohaline circulation (by 30 percent at time of CO2 doubling), the poleward energy transport by the oceans decreases. The colder water then leads to further reductions in evaporation, decreases of salinity at high latitudes, continued stabilization of the ocean, and maintenance of reduced convection and meridional overturning. Although sea ice decreases globally, it increases in the cooling regions which reduces the overall climate sensitivity; its effect is most pronounced in the Southern Hemisphere. Tropical warming has been observed over the past several decades; if modeling studies such as this and others which have produced similar effects are valid, these processes may already be beginning.

Carbon-climate feedbacks accelerate ocean acidification

NASA Astrophysics Data System (ADS)

Matear, Richard J.; Lenton, Andrew

2018-03-01

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

IMBER (Integrated Marine Biogeochemistry and Ecosystem Research: Support of Ocean Carbon Research

NASA Astrophysics Data System (ADS)

Rimetz-Planchon, J.; Gattuso, J.; Maddison, L.; Bakker, D. C.; Gruber, N.

2011-12-01

IMBER (Integrated Marine Biogeochemistry and Ecosystem Research), co-sponsored by SCOR (Scientific Committee on Oceanic Research) and IGBP (International Geosphere-Biosphere Programme), coordinates research that focuses on understanding and predicting changes in oceanic food webs and biogeochemical cycles that arise from global change. An integral part of this overall goal is to understand the marine carbon cycle, with emphasis on changes that may occur as a result of a changing climate, increased atmospheric CO2 levels and/or reduced oceanic pH. To address these key ocean carbon issues, IMBER and SOLAS (Surface Ocean Lower Atmosphere Study), formed the joint SOLAS-IMBER Carbon, or SIC Working Group. The SIC Working Group activities are organised into three sub-groups. Sub-group 1 (Surface Ocean Systems) focuses on synthesis, instrumentation and technology development, VOS (Voluntary Observing Ships) and mixed layer sampling strategies. The group contributed to the development of SOCAT (Surface Ocean CO2 Atlas, www.socat.info), a global compilation of underway surface water fCO2 (fugacity of CO2) data in common format. It includes 6.3 million measurements from 1767 cruises from 1968 and 2008 by more than 10 countries. SOCAT will be publically available and will serve a wide range of user communities. Its public release is planned for September 2011. SOCAT is strongly supported by IOCCP and CARBOOCEAN. Sub-group 2 (Interior Ocean Carbon Storage) covers inventory and observations, natural variability, transformation and interaction with modelling. It coordinated a review of vulnerabilities of the decadal variations of the interior ocean carbon and oxygen cycle. It has also developed a plan to add dissolved oxygen sensors to the ARGO float program in order to address the expected loss of oxygen as a result of ocean warming. The group also focuses on the global synthesis of ocean interior carbon observations to determine the oceanic uptake of anthropogenic CO2 since the mid 1990s. Sub-group 3 (SOLAS-IMBER Ocean Acidification or SIOA) coordinates international research efforts in ocean acidification and undertakes synthesis activities in ocean acidification at the international level. Several on-going synthesis activities, such as book projects and work by the Intergovernmental Panel on Climate Change (IPCC) are endorsed by this group. The SIOA developed a package of activities which it identified as critical to assess the effects of ocean acidification but are, for the most part, not funded at the national or regional levels and must be carried out at the international level. Among them is the promotion of international experiments, the sharing of experimental platforms, and the undertaking of inter-comparison exercises. The SIOA has submitted a proposal to launch an Ocean Acidification International Coordination Office in March 2011. This poster highlights some results from the SIC Working Group and indicates future challenges.

Forward Modeling of Atmospheric Carbon Dioxide in GEOS-5: Uncertainties Related to Surface Fluxes and Sub-Grid Transport

NASA Technical Reports Server (NTRS)

Pawson, Steven; Ott, Lesley E.; Zhu, Zhengxin; Bowman, Kevin; Brix, Holger; Collatz, G. James; Dutkiewicz, Stephanie; Fisher, Joshua B.; Gregg, Watson W.; Hill, Chris;

The reinvigoration of the Southern Ocean carbon sink.

PubMed

Landschützer, Peter; Gruber, Nicolas; Haumann, F Alexander; Rödenbeck, Christian; Bakker, Dorothee C E; van Heuven, Steven; Hoppema, Mario; Metzl, Nicolas; Sweeney, Colm; Takahashi, Taro; Tilbrook, Bronte; Wanninkhof, Rik

2015-09-11

Several studies have suggested that the carbon sink in the Southern Ocean-the ocean's strongest region for the uptake of anthropogenic CO2 -has weakened in recent decades. We demonstrated, on the basis of multidecadal analyses of surface ocean CO2 observations, that this weakening trend stopped around 2002, and by 2012, the Southern Ocean had regained its expected strength based on the growth of atmospheric CO2. All three Southern Ocean sectors have contributed to this reinvigoration of the carbon sink, yet differences in the processes between sectors exist, related to a tendency toward a zonally more asymmetric atmospheric circulation. The large decadal variations in the Southern Ocean carbon sink suggest a rather dynamic ocean carbon cycle that varies more in time than previously recognized. Copyright © 2015, American Association for the Advancement of Science.

Slowing Ocean Acidification

NASA Astrophysics Data System (ADS)

Bravo, A.

2016-12-01

Currently our ocean's pH is 8.1, a decrease from 8.2 in the past 200 years since the beginning of the industrial revolution. The ocean absorbs about a third of the carbon dioxide (CO2) from the atmosphere, which is helpful to us, since reducing the amount of CO2 in the atmosphere shows global warming. However, what is the impact of all that CO2 on the ocean? I evaluated the effect of acidic water on bivalves, and found that the shells were broken down with exposure to increased acidity. I am concerned that continued ocean acidification will impact organisms that are unable to adapt to the changing ocean chemistry. While the US currently invests in alternative forms of energy including solar and wind, approximately 66% of our energy comes from sources that are releasing CO2 into the atmosphere. I want to explore the potential of wave energy as another form of renewable energy. When wind blows over the surface of the ocean, it creates a wave. Could this wave energy be a consistent clean energy source? Could a strategy to slow and reverse ocean acidification be found in the ocean?

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

NASA Astrophysics Data System (ADS)

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

2015-12-01

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

The carbonate-silicate cycle and CO2/climate feedbacks on tidally locked terrestrial planets.

PubMed

Edson, Adam R; Kasting, James F; Pollard, David; Lee, Sukyoung; Bannon, Peter R

2012-06-01

Atmospheric gaseous constituents play an important role in determining the surface temperatures and habitability of a planet. Using a global climate model and a parameterization of the carbonate-silicate cycle, we explored the effect of the location of the substellar point on the atmospheric CO(2) concentration and temperatures of a tidally locked terrestrial planet, using the present Earth continental distribution as an example. We found that the substellar point's location relative to the continents is an important factor in determining weathering and the equilibrium atmospheric CO(2) level. Placing the substellar point over the Atlantic Ocean results in an atmospheric CO(2) concentration of 7 ppmv and a global mean surface air temperature of 247 K, making ∼30% of the planet's surface habitable, whereas placing it over the Pacific Ocean results in a CO(2) concentration of 60,311 ppmv and a global temperature of 282 K, making ∼55% of the surface habitable.

Sensitivity of Ocean Chemistry and Oxygen Change to the Uncertainty in Climate Change

NASA Astrophysics Data System (ADS)

Cao, L.; Wang, S.; Zheng, M.; Zhang, H.

2014-12-01

With increasing atmospheric CO2 and climate change, global ocean is undergoing substantial physical and biogeochemical changes. In particular, changes in ocean oxygen and carbonate chemistry have great implication for marine biota. There is considerable uncertainty in the projections of future climate change, and it is unclear how the uncertainty in climate change would affect the projection of ocean oxygen and carbonate chemistry. To examine the effect of climate change on ocean oxygen and carbonate chemistry, we used an Earth system model of intermediate complexity to perform simulations that are driven by atmospheric CO2 concentration pathway of RCP 8.5 with climate sensitivity varying from 0.0°C to 4.5 °C. Climate change affects carbonate chemistry and oxygen mainly through its impact on ocean temperature, ocean ventilation, and concentration of dissolved inorganic carbon and alkalinity. Our simulations show that climate change mitigates the decrease of carbonate ions at the ocean surface but has negligible effect on surface ocean pH. Averaged over the whole ocean, climate change acts to decrease oxygen concentration but mitigates the CO2-induced reduction of carbonate ion and pH. In our simulations, by year 2500, every degree increase of climate sensitivity warms the ocean by 0.8 °C and reduces ocean-mean dissolved oxygen concentration by 5.0%. Meanwhile, every degree increase of climate sensitivity buffers CO2-induced reduction in ocean-mean carbonate ion concentration and pH by 3.4% and 0.02 units, respectively. Our study demonstrates different sensitivities of ocean temperature, carbonate chemistry, and oxygen, in terms of both the sign and magnitude, to the amount of climate change, which have great implications for understanding the response of ocean biota to climate change.

Monitoring Ocean CO2 Fluxes from Space: GOSAT and OCO-2

NASA Technical Reports Server (NTRS)

Crisp, David

2012-01-01

The ocean is a major component of the global carbon cycle, emitting over 330 billion tons of carbon dioxide (CO2) into the atmosphere each year, or about 10 times that emitted fossil fuel combustion and all other human activities [1, 2]. The ocean reabsorbs a comparable amount of CO2 each year, along with 25% of the CO2 emitted by these human activities. The nature and geographic distribution of the processes controlling these ocean CO2 fluxes are still poorly constrained by observations. A better understanding of these processes is essential to predict how this important CO2 sink may evolve as the climate changes.While in situ measurements of ocean CO2 fluxes can be very precise, the sampling density is far too sparse to quantify ocean CO2 sources and sinks over much of the globe. One way to improve the spatial resolution, coverage, and sampling frequency is to make observations of the column averaged CO2 dry air mole fraction, XCO2, from space [4, 5, 6]. Such measurements could provide global coverage at high resolution (< 100 km) on monthly time scales. High precision (< 1 part per million, ppm) is essential to resolve the small, near-surface CO2 variations associated with ocean fluxes and to better constrain the CO2 transport over the ocean. The Japanese Greenhouse gases Observing Satellite (GOSAT) and the NASA Orbiting Carbon Observatory (OCO) were first two space based sensors designed specifically for this task. GOSAT was successfully launched on January 23, 2009, and has been returning measurements of XCO2 since April 2009. The OCO mission was lost in February 2009, when its launch vehicle malfunctioned and failed to reach orbit. In early 2010, NASA authorized a re-flight of OCO, called OCO-2, which is currently under development.

Spatiotemporal trends in surface seawater CO2 in the Gulf of Mexico

NASA Astrophysics Data System (ADS)

Kealoha, A. K.; Shamberger, K.

2016-12-01

The Gulf of Mexico (GoM) contains many interconnected ecosystems intimately linked to regional economic stability through fisheries. Yet, numerous human pressures, including eutrophication-induced hypoxia and ocean acidification (OA), threaten the health of this large marine ecosystem. A comprehensive characterization of the drivers of GoM seawater CO2 cycling is required to assess interactions between these local stresses, global climate change, and OA. Several observational and modeling studies have been conducted in an effort to characterize CO2-system trends within the GoM. However, observational studies are limited to specific regions and time-frames, while modeled data are based on parameterizations that often cannot account for all the biogeochemical processes occurring in this complex system. Here, we present a compilation of approximately 510,000 continuous, underway measurements of sea surface temperature, salinity and seawater CO2, collected from 1996-2013 throughout the entire GoM. These data reveal distinct spatial and temporal CO2 trends that are driven primarily by temperature, Mississippi River outflow, biological productivity, and water circulation. For example, during the spring and summer, nutrient input from the Mississippi River stimulates biological productivity that drives surface seawater CO2 below atmospheric levels in the north-central GoM shelf waters. Although open ocean waters are generally a source of CO2 to the atmosphere in the summer, a unique combination of physical processes including high river discharge, offshore currents and eddy activity can transport low CO2 coastal water beyond the shelf causing vast areas, tens of thousands of square kilometers, of the open ocean to switch to a CO2 sink for several months. Since anthropogenic-driven climate change is expected to influence ocean circulation patterns, GoM CO2 source-sink characteristics and regional scale ocean carbon budgets may be altered in the future. We also combine discrete CO2 chemistry data collected in the Flower Garden Banks National Marine Sanctuary with historical underway data to provide insight into the connections between Gulf wide carbon variability and variability within these important coral reef ecosystems.

Iron fertilisation and century-scale effects of open ocean dissolution of olivine in a simulated CO2 removal experiment

NASA Astrophysics Data System (ADS)

Hauck, Judith; Köhler, Peter; Wolf-Gladrow, Dieter; Völker, Christoph

2016-02-01

Carbon dioxide removal (CDR) approaches are efforts to reduce the atmospheric CO2 concentration. Here we use a marine carbon cycle model to investigate the effects of one CDR technique: the open ocean dissolution of the iron-containing mineral olivine. We analyse the maximum CDR potential of an annual dissolution of 3 Pg olivine during the 21st century and focus on the role of the micro-nutrient iron for the biological carbon pump. Distributing the products of olivine dissolution (bicarbonate, silicic acid, iron) uniformly in the global surface ocean has a maximum CDR potential of 0.57 gC/g-olivine mainly due to the alkalinisation of the ocean, with a significant contribution from the fertilisation of phytoplankton with silicic acid and iron. The part of the CDR caused by ocean fertilisation is not permanent, while the CO2 sequestered by alkalinisation would be stored in the ocean as long as alkalinity is not removed from the system. For high CO2 emission scenarios the CDR potential due to the alkalinity input becomes more efficient over time with increasing ocean acidification. The alkalinity-induced CDR potential scales linearly with the amount of olivine, while the iron-induced CDR saturates at 113 PgC per century (on average ˜ 1.1 PgC yr-1) for an iron input rate of 2.3 Tg Fe yr-1 (1% of the iron contained in 3 Pg olivine). The additional iron-related CO2 uptake occurs in the Southern Ocean and in the iron-limited regions of the Pacific. Effects of this approach on surface ocean pH are small (\\lt 0.01).

The Relative Influence of H2O and CO2 on the Primitive Surface Conditions and Evolution of Rocky Planets

NASA Astrophysics Data System (ADS)

Salvador, A.; Massol, H.; Davaille, A.; Marcq, E.; Sarda, P.; Chassefiere, E.

2016-12-01

Recent literature reveals how different the telluric planets' water content can be, depending on the formation processes and origins of water. Furthermore, for Earth mass planets, estimates of their atmospheric water content range between 0.3 to 1000 water oceans. We simulate the secular convective cooling and solidification of a 1D magma ocean (hereafter "MO") in interaction with the outgassed atmosphere. We vary the initial CO2 and H2O contents (respectively from 0.1×10-2 to 14×10-2wt% and from 0.05 to 2.2 times the Earth Ocean current mass (MEO)), the solar distance - from 0.63 to 1.30 AU -, the radiative heat transfer in the atmosphere (grey or non-grey, with or without clouds) and investigate the relative influence of these parameters on an Earth like planet's surface conditions at the MO phase term, and especially its ability to form a water ocean. We define the end of the MO as the time when the heat flux from the vigorous convecting mantle becomes negligible compared to the incident solar flux, linked to the dramatic increase of viscosity as the MO solidification reaches the surface, which considerably reduces the convection intensity and the heat transfer. This particular time coincides with the possible apparition of a water ocean and with the development of a thermal boundary layer at the surface, thick enough to limit the interactions between the two reservoirs. As a first step, we assume a bottom-up solidification of the MO. The planetary surface pressure-temperature conditions, resulting from the solidification, are conditioned by the sun-planet distance and the initial CO2 and H2O contents. There is a critical sun-planet distance Rc below which water will never condense, whatever the initial volatile content. For distances larger than Rc, water condensation strongly depends on the relative proportion of CO2 and H2O. The higher the H2O content, the easier it is to reach the equilibrium water vapor pressure and therefore to condense water, for the tested range of CO2 contents. Otherwise, for [H2O]t0<1.8 MEO , too much CO2 precludes the formation of a water ocean by greenhouse effect. In order to study exoplanets surface conditions, and the wide diversity of these gas rich extrasolar worlds, we propose a simple scaling law to explain the relative influence of the tested parameters on the water condensation.

Quantifying the drivers of ocean-atmosphere CO2 fluxes

NASA Astrophysics Data System (ADS)

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.

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

NASA Astrophysics Data System (ADS)

Oschlies, A.

2009-08-01

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

Calculating surface ocean pCO2 from biogeochemical Argo floats equipped with pH: An uncertainty analysis

NASA Astrophysics Data System (ADS)

Williams, N. L.; Juranek, L. W.; Feely, R. A.; Johnson, K. S.; Sarmiento, J. L.; Talley, L. D.; Dickson, A. G.; Gray, A. R.; Wanninkhof, R.; Russell, J. L.; Riser, S. C.; Takeshita, Y.

2017-03-01

More than 74 biogeochemical profiling floats that measure water column pH, oxygen, nitrate, fluorescence, and backscattering at 10 day intervals have been deployed throughout the Southern Ocean. Calculating the surface ocean partial pressure of carbon dioxide (pCO2sw) from float pH has uncertainty contributions from the pH sensor, the alkalinity estimate, and carbonate system equilibrium constants, resulting in a relative standard uncertainty in pCO2sw of 2.7% (or 11 µatm at pCO2sw of 400 µatm). The calculated pCO2sw from several floats spanning a range of oceanographic regimes are compared to existing climatologies. In some locations, such as the subantarctic zone, the float data closely match the climatologies, but in the polar Antarctic zone significantly higher pCO2sw are calculated in the wintertime implying a greater air-sea CO2 efflux estimate. Our results based on four representative floats suggest that despite their uncertainty relative to direct measurements, the float data can be used to improve estimates for air-sea carbon flux, as well as to increase knowledge of spatial, seasonal, and interannual variability in this flux.

Sequestering CO2 in the Ocean: Options and Consequences

NASA Astrophysics Data System (ADS)

Rau, G. H.; Caldeira, K.

2002-12-01

The likelihood of negative climate and environmental impacts associated with increasing atmospheric CO2 has prompted serious consideration of various CO2 mitigation strategies. Among these are methods of capturing and storing of CO2 in the ocean. Two approaches that have received the most attention in this regard have been i) ocean fertilization to enhanced biological uptake and fixation of CO2, and ii) the chemical/mechanical capture and injection of CO2 into the deep ocean. Both methods seek to enhance or speed up natural mechanisms of CO2 uptake and storage by the ocean, namely i) the biological CO2 "pump" or ii) the passive diffusion of CO2 into the surface ocean and subsequent mixing into the deep sea. However, as will be reviewed, concerns about the capacity and effectiveness of either strategy in long-term CO2 sequestration have been raised. Both methods are not without potentially significant environmental impacts, and the costs of CO2 capture and injection (option ii) are currently prohibitive. An alternate method of ocean CO2 sequestration would be to react and hydrate CO2 rich waste gases (e.g., power plant flue gas) with seawater and to subsequently neutralize the resulting carbonic acid with limestone to produce calcium and bicarbonate ions in solution. This approach would simply speed up the CO2 uptake and sequestration that naturally (but very slowly) occurs via global carbonate weathering. This would avoid much of the increased acidity associated with direct CO2 injection while obviating the need for costly CO2 separation and capture. The addition of the resulting bicarbonate- and carbonate-rich solution to the ocean would help to counter the decrease in pH and carbonate ion concentration, and hence loss of biological calcification that is presently occurring as anthropogenic CO2 invades the ocean from the atmosphere. However, as with any approach to CO2 mitigation, the costs, impacts, risks, and benefits of this method need to be better understood and weighed against those of alternative strategies, including business as usual.

The Impact of Ocean Acidification on the Functional Morphology of Foraminifera

PubMed Central

Khanna, Nikki; Godbold, Jasmin A.; Austin, William E. N.; Paterson, David M.

2013-01-01

Culturing experiments were performed on sediment samples from the Ythan Estuary, N. E. Scotland, to assess the impacts of ocean acidification on test surface ornamentation in the benthic foraminifer Haynesina germanica. Specimens were cultured for 36 weeks at either 380, 750 or 1000 ppm atmospheric CO2. Analysis of the test surface using SEM imaging reveals sensitivity of functionally important ornamentation associated with feeding to changing seawater CO2 levels. Specimens incubated at high CO2 levels displayed evidence of shell dissolution, a significant reduction and deformation of ornamentation. It is clear that these calcifying organisms are likely to be vulnerable to ocean acidification. A reduction in functionally important ornamentation could lead to a reduction in feeding efficiency with consequent impacts on this organism's survival and fitness. PMID:24358253

The Active Role of the Ocean in the Temporal Evolution of Climate Sensitivity

DOE PAGES

Garuba, Oluwayemi A.; Lu, Jian; Liu, Fukai; ...

2017-11-30

Here, the temporal evolution of the effective climate sensitivity is shown to be influenced by the changing pattern of sea surface temperature (SST) and ocean heat uptake (OHU), which in turn have been attributed to ocean circulation changes. A set of novel experiments are performed to isolate the active role of the ocean by comparing a fully coupled CO 2 quadrupling community Earth System Model (CESM) simulation against a partially coupled one, where the effect of the ocean circulation change and its impact on surface fluxes are disabled. The active OHU is responsible for the reduced effective climate sensitivity andmore » weaker surface warming response in the fully coupled simulation. The passive OHU excites qualitatively similar feedbacks to CO 2 quadrupling in a slab ocean model configuration due to the similar SST spatial pattern response in both experiments. Additionally, the nonunitary forcing efficacy of the active OHU (1.7) explains the very different net feedback parameters in the fully and partially coupled responses.« less

The Active Role of the Ocean in the Temporal Evolution of Climate Sensitivity

NASA Astrophysics Data System (ADS)

Garuba, Oluwayemi A.; Lu, Jian; Liu, Fukai; Singh, Hansi A.

2018-01-01

The temporal evolution of the effective climate sensitivity is shown to be influenced by the changing pattern of sea surface temperature (SST) and ocean heat uptake (OHU), which in turn have been attributed to ocean circulation changes. A set of novel experiments are performed to isolate the active role of the ocean by comparing a fully coupled CO2 quadrupling community Earth System Model (CESM) simulation against a partially coupled one, where the effect of the ocean circulation change and its impact on surface fluxes are disabled. The active OHU is responsible for the reduced effective climate sensitivity and weaker surface warming response in the fully coupled simulation. The passive OHU excites qualitatively similar feedbacks to CO2 quadrupling in a slab ocean model configuration due to the similar SST spatial pattern response in both experiments. Additionally, the nonunitary forcing efficacy of the active OHU (1.7) explains the very different net feedback parameters in the fully and partially coupled responses.

The Active Role of the Ocean in the Temporal Evolution of Climate Sensitivity

DOE Office of Scientific and Technical Information (OSTI.GOV)

Garuba, Oluwayemi A.; Lu, Jian; Liu, Fukai

Here, the temporal evolution of the effective climate sensitivity is shown to be influenced by the changing pattern of sea surface temperature (SST) and ocean heat uptake (OHU), which in turn have been attributed to ocean circulation changes. A set of novel experiments are performed to isolate the active role of the ocean by comparing a fully coupled CO 2 quadrupling community Earth System Model (CESM) simulation against a partially coupled one, where the effect of the ocean circulation change and its impact on surface fluxes are disabled. The active OHU is responsible for the reduced effective climate sensitivity andmore » weaker surface warming response in the fully coupled simulation. The passive OHU excites qualitatively similar feedbacks to CO 2 quadrupling in a slab ocean model configuration due to the similar SST spatial pattern response in both experiments. Additionally, the nonunitary forcing efficacy of the active OHU (1.7) explains the very different net feedback parameters in the fully and partially coupled responses.« less

Modeling the Impact of Forest and Peat Fires on Carbon-Isotopic Compositions of Cretaceous Atmosphere and Vegetation

NASA Astrophysics Data System (ADS)

Finkelstein, D. B.; Pratt, L. M.

2004-12-01

Prevalence of wildfires or peat fires associated with seasonally dry conditions in the Cretaceous is supported by recent studies documenting the widespread presence of pyrolytic polycyclic aromatic hydrocarbons and fusinite. Potential roles of CO2 emissions from fire have been overlooked in many discussions of Cretaceous carbon-isotope excursions (excluding K-P boundary discussions). Enhanced atmospheric CO2 levels could increase fire frequency through elevated lightning activity. When biomass or peat is combusted, emissions of CO2 are more negative than atmospheric CO2. Five reservoirs (atmosphere, vegetation, soil, and shallow and deep oceans), and five fluxes (productivity, respiration, litter fall, atmosphere-ocean exchange, and surface-deep ocean exchange) were modeled as a closed system. The size of the Cretaceous peat reservoir was estimated by compilation of published early Cretaceous coal resources. Initial pCO2 was assumed to be 2x pre-industrial atmospheric levels (P.A.L.). Critical variables in the model are burning efficiency and post-fire growth rates. Assuming 1% of standing terrestrial biomass is consumed by wildfires each year for ten years (without combustion of peat), an increase of atmospheric CO2 (from 2.0 to 2.2x P.A.L.) and a negative carbon isotope excursion (-1.2 ‰ ) are recorded by both atmosphere and new growth. Net primary productivity linked to the residence time of the vegetation and soil reservoirs results in a negative isotope shift followed by a broad positive isotope excursion. Decreasing the rate of re-growth dampens this trailing positive shift and increases the duration of the excursion. Post-fire pCO2 and new growth returned to initial values after 72 years. Both negative and positive isotope excursions are recorded in the model in surface ocean waters. Exchange of CO2 with the surface- and deep-ocean dampens the isotopic shift of the atmosphere. Excursions are first recorded in the atmosphere (and new growth), followed by the ocean, vegetation, and soil reservoirs. Ten to twenty five-year cycles of drought and fire are not recorded as individual excursions in the soil reservoir as the rate of transfer between the vegetation and soil reservoirs homogenizes the signal. A wildfire-modeled excursion does not propagate a geologically significant excursion through time. Combustion of a peat reservoir is necessary to drive and validate a geologically and isotopically significant excursion. Assuming 0.5% of the standing early Cretaceous peat reservoir is consumed by fire for each year for ten years coupled with the earlier scenario, the atmospheric CO2 increases from 2.0 to 3.1x P.A.L., atmosphere, vegetation, and the surface ocean record a negative carbon isotope excursion of -5.1 ‰ , -3.8 ‰ and -1.8 ‰ respectively, with a duration of 741 years. Increasing the size of the vegetation reservoir translates the excursions from the centennial to millennial scale. For example, doubling the vegetation reservoir (from 1.4 to 2.8E+16 gC) for a 25 year global peat conflagration (0.5% combusted each year) results in a CO2 increase from 2.0 to 4.0x P.A.L., and the atmosphere, vegetation, and the surface ocean reservoirs with a negative carbon isotope excursion of -5.7 ‰ , -8.7 ‰ and -2.3 ‰ respectively. Addition of carbonaceous aerosols (black carbon and polycyclic aromatic hydrocarbons) to pelagic marine sediments could potentially serve as a high-resolution record of ancient fires and firmly tie isotopic shifts to paleofires.

High pCO2-induced exopolysaccharide-rich ballasted aggregates of planktonic cyanobacteria could explain Paleoproterozoic carbon burial.

PubMed

Kamennaya, Nina A; Zemla, Marcin; Mahoney, Laura; Chen, Liang; Holman, Elizabeth; Holman, Hoi-Ying; Auer, Manfred; Ajo-Franklin, Caroline M; Jansson, Christer

2018-05-29

The contribution of planktonic cyanobacteria to burial of organic carbon in deep-sea sediments before the emergence of eukaryotic predators ~1.5 Ga has been considered negligible owing to the slow sinking speed of their small cells. However, global, highly positive excursion in carbon isotope values of inorganic carbonates ~2.22-2.06 Ga implies massive organic matter burial that had to be linked to oceanic cyanobacteria. Here to elucidate that link, we experiment with unicellular planktonic cyanobacteria acclimated to high partial CO 2 pressure (pCO 2 ) representative of the early Paleoproterozoic. We find that high pCO 2 boosts generation of acidic extracellular polysaccharides (EPS) that adsorb Ca and Mg cations, support mineralization, and aggregate cells to form ballasted particles. The down flux of such self-assembled cyanobacterial aggregates would decouple the oxygenic photosynthesis from oxidative respiration at the ocean scale, drive export of organic matter from surface to deep ocean and sustain oxygenation of the planetary surface.

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

NASA Astrophysics Data System (ADS)

Oschlies, A.

2009-04-01

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

Biogeochemical linkage between atmosphere and ocean in the eastern equatorial Pacific Ocean: Results from the EqPOS research cruise

NASA Astrophysics Data System (ADS)

Furutani, H.; Inai, Y.; Aoki, S.; Honda, H.; Omori, Y.; Tanimoto, H.; Iwata, T.; Ueda, S.; Miura, K.; Uematsu, M.

2012-12-01

Eastern equatorial Pacific Ocean is a unique oceanic region from several biogeochemical points of view. It is a remote open ocean with relatively high marine biological activity, which would result in limited influence of human activity but enhanced effect of marine natural processes on atmospheric composition. It is also characterized as high nutrient low chlorophyll (HNLC) ocean, in which availability of trace metals such as iron and zinc limits marine primary production and thus atmospheric deposition of these trace elements to the ocean surface is expected to play an important role in regulating marine primary production and defining unique microbial community. High sea surface temperature in the region generates strong vertical air convection which efficiently brings tropospheric atmospheric composition into stratosphere. In this unique eastern equatorial Pacific Ocean, EqPOS (Equatorial Pacific Ocean and Stratospheric/Tropospheric Atmospheric Study) research cruise was organized as a part of SOLAS Japan activity to understand biogeochemical ocean-atmospheric interaction in the region. Coordinated atmospheric, oceanic, and marine biological observations including sampling/characterization of thin air-sea interfacial layer (sea surface microlayer: SML) and launching large stratospheric air sampling balloons were carried out on-board R/V Hakuho Maru starting from 29 January for 39 days. Biogeochemically important trace/long-lived gases such as CO2, dimethyl sulfide (DMS), and some volatile organic carbons (VOCs) both in the atmosphere and seawater were continuously monitored and their air-sea fluxes were also observed using gradient and eddy-covariance techniques. Atmospheric gas measurement of CO2, CH4, N2O, SF6, CO, H2, Ar and isotopic composition of selected gases were further extended to stratospheric air by balloon-born sampling in addition to a vertical profiling of O3, CO2, and H2O with sounding sondes. Physical and chemical properties of marine atmospheric aerosols such as size distribution, total and cloud condensation nuclei concentrations, particle morphology, bulk and single particle chemical composition were also continuously determined to find out potential link between biogenic VOCs emitted from the ocean and aerosol composition. Biological and biogeochemical characterizations of marine microorganisms, suspended particulate matter, dissolved nutrients in seawater and SML were also conducted. In the presentation, brief overview of the research activities during the EqPOS cruise and biogeochemical linkage atmosphere and ocean via atmospheric and oceanic gaseous and particulate matter from ocean surface to stratosphere observed during the cruise and unique importance of SML would be presented.

CO/sub 2/ fluxes in the tropical Atlantic during FOCAL cruises

DOE Office of Scientific and Technical Information (OSTI.GOV)

Andrie, C.; Oudot, C.; Genthon, C.

1986-10-15

CO/sub 2/ partial pressures in the atmosphere and in surface seawater have been measured in the equatorial Atlantic Ocean during Programme Francais Ocean-Climat en Atlantique Equatorial cruises extending from July 1982 to August 1984 along the 4/degree/W, 22/degree/W, and 35/degree/W meridians. Gas transfer coefficients based on recently reported field data combined with information deduced from wind tunnel experiments are used to compute the CO/sub 2/ fluxes. The global mean net flux between 5/degree/N and 5/degree/S is equal to 1.05 mmol m/sup /minus/2/ d/sup /minus/1/ and is from the ocean to the atmosphere. The escape of CO/sub 2/ increases strongly frommore » the east to the west and is always lower in the north than in the south. The importance of wind speed, pCO/sub 2/ in atmosphere, PCO/sub 2/ in surface seawater, and temperature on the flux variability is discussed. The relative influence of the equatorial upwelling on one hand and of the advection and warming of surface waters on the other hand is studied in order to explain high partial pressure in seawater. 59 refs., 15 figs., 5 tabs.« less

Satellite Evidence that E. huxleyi Phytoplankton Blooms Weaken Marine Carbon Sinks

NASA Astrophysics Data System (ADS)

Kondrik, D. V.; Pozdnyakov, D. V.; Johannessen, O. M.

2018-01-01

Phytoplankton blooms of the coccolithophore Emiliania huxleyi are known to produce CO2, causing less uptake of atmospheric CO2 by the ocean, but a global assessment of this phenomenon has so far not been quantified. Therefore, here we quantify the increase in CO2 partial pressure (ΔpCO2) at the ocean surface within E. huxleyi blooms for polar and subpolar seas using an 18 year ocean color time series (1998-2015). When normalized to pCO2 in the absence of bloom, the mean and maximum ΔpCO2 values within the bloom areas varied between 21.0%-43.3% and 31.6%-62.5%, respectively. These results might have appreciable implications for climatology, marine chemistry, and ecology.

Seasonal controls of the short term variability of pCO2 at the Scotian Shelf

NASA Astrophysics Data System (ADS)

Thomas, H.; Craig, S.; Greenan, B. J. W.; Burt, W.; Herndl, G. J.; Higginson, S.; Salt, L.; Shadwick, E. H.; Urrego-Blanco, J.

2012-04-01

Much of the surface ocean carbon cycle variability can be attributed to the availability of sunlight, through processes such as heat fluxes or photosynthesis, which regulate the ocean carbon cycle over a wide range of time scales. The critical processes occurring on timescales of a day or less, however, have undergone few investigations, and most of those have been limited to a time span of several days to months, or exceptionally, for longer periods. Optical methods have helped to infer short-term biological variability, however lacking corresponding investigations of oceanic CO2 system. Here, we employ high-frequency CO2 system and optical observations covering the full seasonal cycle on the Scotian Shelf, Northwestern Atlantic Ocean, in order to unravel daily periodicity of the surface ocean carbon cycle and its effects on annual budgets. We show that significant daily periodicity occurs only if the water column is sufficiently stable as observed during seasonal warming. During that time biological CO2 drawdown, or net community production (NCP), is delayed for several hours relative to the daylight cycle due the daily build-up of essential Chlorophyll a, to cell physiology and to grazing effects, all restricting or hindering photosynthesis in the early morning hours. NCP collapses in summer by more than 90%, when the mixed layer depth reaches the seasonal minimum, which eventually makes the observed daily periodicity of the CO2 system vanish.

Replenishment of fish populations is threatened by ocean acidification

PubMed Central

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

2010-01-01

There is increasing concern that ocean acidification, caused by the uptake of additional CO2 at the ocean surface, could affect the functioning of marine ecosystems; however, the mechanisms by which population declines will occur have not been identified, especially for noncalcifying species such as fishes. Here, we use a combination of laboratory and field-based experiments to show that levels of dissolved CO2 predicted to occur in the ocean this century alter the behavior of larval fish and dramatically decrease their survival during recruitment to adult populations. Altered behavior of larvae was detected at 700 ppm CO2, with many individuals becoming attracted to the smell of predators. At 850 ppm CO2, the ability to sense predators was completely impaired. Larvae exposed to elevated CO2 were more active and exhibited riskier behavior in natural coral-reef habitat. As a result, they had 5–9 times higher mortality from predation than current-day controls, with mortality increasing with CO2 concentration. Our results show that additional CO2 absorbed into the ocean will reduce recruitment success and have far-reaching consequences for the sustainability of fish populations. PMID:20615968

Gas exchange and CO2 flux in the tropical Atlantic Ocean determined from Rn-222 and pCO2 measurements

NASA Technical Reports Server (NTRS)

Smethie, W. M., Jr.; Takahashi, T.; Chipman, D. W.; Ledwell, J. R.

1985-01-01

The piston velocity for the tropical Atlantic Ocean has been determined from 29 radon profiles measured during the TTO Tropical Atlantic Study. By combining these data with the pCO2 data measured in the surface water and air samples, the net flux of CO2 across the sea-air interface has been calculated for the tropical Atlantic. The dependence of the piston velocity on wind speed is discussed, and possible causes for the high sea-to-air CO2 flux observed in the equatorial zone are examined.

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

DOE Office of Scientific and Technical Information (OSTI.GOV)

Singh, H. A.; Rasch, P. J.; Rose, B. E. J.

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

Increased Ocean Heat Convergence Into the High Latitudes With CO2 Doubling Enhances Polar-Amplified Warming

NASA Astrophysics Data System (ADS)

Singh, H. A.; Rasch, P. J.; Rose, B. E. J.

2017-10-01

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

Glacial CO2 Cycles: A Composite Scenario

NASA Astrophysics Data System (ADS)

Broecker, W. S.

2015-12-01

There are three main contributors to the glacial drawdown of atmospheric CO2 content: starvation of the supply of carbon to the ocean-atmosphere reservoir, excess CO2 storage in the deep sea, and surface-ocean cooling. In this talk, I explore a scenario in which all three play significant roles. Key to this scenario is the assumption that deep ocean storage is related to the extent of nutrient stratification of the deep Atlantic. The stronger this stratification, the larger the storage of respiration CO2. Further, it is my contention that the link between Milankovitch insolation cycles and climate is reorganizations of the ocean's thermohaline circulation leading to changes in the deep ocean's CO2 storage. If this is the case, the deep Atlantic d13C record kept in benthic foraminifera shells tells us that deep ocean CO2 storage follows Northern Hemisphere summer insolation cycles and thus lacks the downward ramp so prominent in the records of sea level, benthic 18O and CO2. Rather, the ramp is created by the damping of planetary CO2 emissions during glacial time intervals. As it is premature to present a specific scenario, I provide an example as to how these three contributors might be combined. As their magnitudes and shapes remain largely unconstrained, the intent of this exercise is to provoke creative thinking.

Atmospheric radiocarbon as a Southern Ocean wind proxy over the last 1000 years

NASA Astrophysics Data System (ADS)

Rodgers, K. B.; Mikaloff Fletcher, S.; Galbraith, E.; Sarmiento, J. L.; Gnanadesikan, A.; Slater, R. D.; Naegler, T.

2009-04-01

Measurements of radiocarbon in tree rings over the last 1000 years indicate that there was a pre-industrial latitudinal gradient of atmospheric radiocarbon of 3.9-4.5 per mail and that this gradient had temporal variability of order 6 per mil. Here we test the idea that the mean gradient as well as variability in he gradient is dominated by the strength of the winds over the Southern Ocean. This is done using an ocean model and an atmospheric transport model. The ocean model is used to derive fluxes of 12CO2 and 14CO2 at the sea surface, and these fluxes are used as a lower boundary condition for the transport model. For the mean state, strong winds in the Southern Ocean drive significant upwelling of radiocarbon-depleted Circumpolar Deep Water (CDW), leading to a net flux of 14CO2 relative to 12CO2 into the ocean. This serves to maintain a hemispheric gradient in pre-anthropogenic atmospheric delta-c14. For perturbations, increased/decreased Southern Ocean winds drive increased/decreased uptake of 14CO2 relative to 12CO2, thus increasing/decreasing the hemispheric gradient in atmospheric delta-c14. The tree ring data is interpreted to reveal a decrease in the strength of the Southern Ocean winds at the transition between the Little Ice Age and the Medieval Warm Period.

Interannual variability of primary production and air-sea CO2 flux in the Atlantic and Indian sectors of the Southern Ocean.

NASA Astrophysics Data System (ADS)

Dufour, Carolina; Merlivat, Liliane; Le Sommer, Julien; Boutin, Jacqueline; Antoine, David

2013-04-01

As one of the major oceanic sinks of anthropogenic CO2, the Southern Ocean plays a critical role in the climate system. However, due to the scarcity of observations, little is known about physical and biological processes that control air-sea CO2 fluxes and how these processes might respond to climate change. It is well established that primary production is one of the major drivers of air-sea CO2 fluxes, consuming surface Dissolved Inorganic Carbon (DIC) during Summer. Southern Ocean primary production is though constrained by several limiting factors such as iron and light availability, which are both sensitive to mixed layer depth. Mixed layer depth is known to be affected by current changes in wind stress or freshwater fluxes over the Southern Ocean. But we still don't know how primary production may respond to anomalous mixed layer depth neither how physical processes may balance this response to set the seasonal cycle of air-sea CO2 fluxes. In this study, we investigate the impact of anomalous mixed layer depth on surface DIC in the Atlantic and Indian sectors of the Subantarctic zone of the Southern Ocean (60W-60E, 38S-55S) with a combination of in situ data, satellite data and model experiment. We use both a regional eddy permitting ocean biogeochemical model simulation based on NEMO-PISCES and data-based reconstruction of biogeochemical fields based on CARIOCA buoys and SeaWiFS data. A decomposition of the physical and biological processes driving the seasonal variability of surface DIC is performed with both the model data and observations. A good agreement is found between the model and the data for the amplitude of biological and air-sea flux contributions. The model data are further used to investigate the impact of winter and summer anomalies in mixed layer depth on surface DIC over the period 1990-2004. The relative changes of each physical and biological process contribution are quantified and discussed.

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

NASA Astrophysics Data System (ADS)

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.

Pleistocene atmospheric CO2 change linked to Southern Ocean nutrient utilization

NASA Astrophysics Data System (ADS)

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

2011-12-01

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

Climate warming due to increasing atmospheric CO2 - Simulations with a multilayer coupled atmosphere-ocean seasonal energy balance model

NASA Technical Reports Server (NTRS)

Li, Peng; Chou, Ming-Dah; Arking, Albert

1987-01-01

The transient response of the climate to increasing CO2 is studied using a modified version of the multilayer energy balance model of Peng et al. (1982). The main characteristics of the model are described. Latitudinal and seasonal distributions of planetary albedo, latitude-time distributions of zonal mean temperatures, and latitudinal distributions of evaporation, water vapor transport, and snow cover generated from the model and derived from actual observations are analyzed and compared. It is observed that in response to an atmospheric doubling of CO2, the model reaches within 1/e of the equilibrium response of global mean surface temperature in 9-35 years for the probable range of vertical heat diffusivity in the ocean. For CO2 increases projected by the National Research Council (1983), the model's transient response in annually and globally averaged surface temperatures is 60-75 percent of the corresponding equilibrium response, and the disequilibrium increases with increasing heat diffusivity of the ocean.

Uptake and storage of anthropogenic CO2 in the pacific ocean estimated using two modeling approaches

NASA Astrophysics Data System (ADS)

Li, Yangchun; Xu, Yongfu

2012-07-01

A basin-wide ocean general circulation model (OGCM) of the Pacific Ocean is employed to estimate the uptake and storage of anthropogenic CO2 using two different simulation approaches. The simulation (named BIO) makes use of a carbon model with biological processes and full thermodynamic equations to calculate surface water partial pressure of CO2, whereas the other simulation (named PTB) makes use of a perturbation approach to calculate surface water partial pressure of anthropogenic CO2. The results from the two simulations agree well with the estimates based on observation data in most important aspects of the vertical distribution as well as the total inventory of anthropogenic carbon. The storage of anthropogenic carbon from BIO is closer to the observation-based estimate than that from PTB. The Revelle factor in 1994 obtained in BIO is generally larger than that obtained in PTB in the whole Pacific, except for the subtropical South Pacific. This, to large extent, leads to the difference in the surface anthropogenic CO2 concentration between the two runs. The relative difference in the annual uptake between the two runs is almost constant during the integration processes after 1850. This is probably not caused by dissolved inorganic carbon (DIC), but rather by a factor independent of time. In both runs, the rate of change in anthropogenic CO2 fluxes with time is consistent with the rate of change in the growth rate of atmospheric partial pressure of CO2.

A Sensitivity Analysis of the Impact of Rain on Regional and Global Sea-Air Fluxes of CO2

PubMed Central

Shutler, J. D.; Land, P. E.; Woolf, D. K.; Quartly, G. D.

2016-01-01

The global oceans are considered a major sink of atmospheric carbon dioxide (CO2). Rain is known to alter the physical and chemical conditions at the sea surface, and thus influence the transfer of CO2 between the ocean and atmosphere. It can influence gas exchange through enhanced gas transfer velocity, the direct export of carbon from the atmosphere to the ocean, by altering the sea skin temperature, and through surface layer dilution. However, to date, very few studies quantifying these effects on global net sea-air fluxes exist. Here, we include terms for the enhanced gas transfer velocity and the direct export of carbon in calculations of the global net sea-air fluxes, using a 7-year time series of monthly global climate quality satellite remote sensing observations, model and in-situ data. The use of a non-linear relationship between the effects of rain and wind significantly reduces the estimated impact of rain-induced surface turbulence on the rate of sea-air gas transfer, when compared to a linear relationship. Nevertheless, globally, the rain enhanced gas transfer and rain induced direct export increase the estimated annual oceanic integrated net sink of CO2 by up to 6%. Regionally, the variations can be larger, with rain increasing the estimated annual net sink in the Pacific Ocean by up to 15% and altering monthly net flux by > ± 50%. Based on these analyses, the impacts of rain should be included in the uncertainty analysis of studies that estimate net sea-air fluxes of CO2 as the rain can have a considerable impact, dependent upon the region and timescale. PMID:27673683

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

NASA Astrophysics Data System (ADS)

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.

Natural variability of pCO2 and pH in the Atlantic and Pacific coastal margins of the U.S

NASA Astrophysics Data System (ADS)

Sutton, A. J.; Sabine, C. L.; Feely, R. A.; Newton, J.; Salisbury, J.; Vandemark, D. C.; Musielewicz, S. B.; Maenner-Jones, S.; Bott, R.; Lawrence-Slavas, N.

2011-12-01

The discovery that seawater chemistry is changing as a result of carbon dioxide (CO2) emissions, referred to as "ocean acidification", has prompted a large effort to understand how this changing chemistry will impact marine life. Changes in carbon chemistry have been documented in the open ocean; however, in dynamic coastal systems where many marine species live, ocean acidification and the natural biogeochemical variability that organisms are currently exposed to are poorly quantified. In 2010 we began equipping coastal moorings currently measuring pCO2 with pH and other biogeochemical sensors to measure ocean acidification parameters at 3 hour intervals in the surface water. Here we present the magnitude and diurnal to seasonal variability of pCO2 and pH during the first year of observations at 2 sites in the Atlantic and Pacific coastal margins of the U.S.: the Gulf of Maine and outer coast of Washington state. Both the magnitude and range of pCO2 and pH values were much greater at the coastal moorings compared to the open ocean mooring at Ocean Station Papa in the North Pacific and also varied between the two coastal mooring sites. We observed maximum pCO2 values in coastal waters exceeding predicted values for the open ocean at 2x pre-industrial CO2 levels. The range of pCO2 and pH values during this time series was approximately 4 times the range observed at open ocean mooring Papa (2007-2011 time series). In many cases, large variance was observed at short time scales, with values fluctuating more than 200 μatm pCO2 and 0.2 pH between 3-hour cycles. These types of observations are critical for understanding how ocean acidification will manifest in naturally dynamic coastal systems and for informing the experimental design of species response studies that aim to mimic carbon chemistry experienced by coastal marine organisms.

A History of Warming Sea Surface Temperature and Ocean Acidification Recorded by Planktonic Foraminifera Geochemistry from the Santa Barbara Basin, California

NASA Astrophysics Data System (ADS)

Osborne, E.; Thunell, R.; Bizimis, M.; Buckley, W. P., Jr.; benitez-Nelson, C. R.; Chartier, C. J.

2015-12-01

The geochemistry of foraminiferal shells has been widely used to reconstruct past conditions of the ocean and climate. Since the onset of the Industrial Revolution, anthropogenically produced CO2 has resulted in an increase in global temperatures and a decline in the mean pH of the world's oceans. The California Current System is a particularly susceptible region to ocean acidification due to natural upwelling processes that also cause a reduction in seawater pH. The trace element concentration of magnesium and boron in planktonic foraminiferal shells are used here as proxies for temperature and carbonate ion concentration ([CO32-]), respectively. Newly developed calibrations relating Mg/Ca ratios to temperature (R2 0.91) and B/Ca ratios to [CO32-] (R2 0.84) for the surface-mixed layer species Globogerina bulloides were generated using material collected in the Santa Barbara Basin sediment trap time-series. Using these empirical relationships, temperature and [CO32-] are reconstructed using a 0.5 meter long multi-core collected within the basin. 210Pb activities were used to determine a sedimentation rate for the core to estimate ages for core samples (sedimentation rate: 0.341 cm/yr). A spike in 137Cs activity is used as a tie-point to the year 1965 coinciding with the peak of nuclear bomb testing. Our down-core record extends through the mid-19th century to create a history of rising sea surface temperatures and declining [CO32-] as a result of anthropogenic CO2 emissions.

Phytoplankton Do Not Produce Carbon-Rich Organic Matter in High CO2 Oceans

NASA Astrophysics Data System (ADS)

Kim, Ja-Myung; Lee, Kitack; Suh, Young-Sang; Han, In-Seong

2018-05-01

The ocean is a substantial sink for atmospheric carbon dioxide (CO2) released as a result of human activities. Over the coming decades the dissolved inorganic C concentration in the surface ocean is predicted to increase, which is expected to have a direct influence on the efficiency of C utilization (consumption and production) by phytoplankton during photosynthesis. Here we evaluated the generality of C-rich organic matter production by examining the elemental C:N ratio of organic matter produced under conditions of varying pCO2. The data used in this analysis were obtained from a series of pelagic in situ pCO2 perturbation studies that were performed in the diverse ocean regions and involved natural phytoplankton assemblages. The C:N ratio of the resulting particulate and dissolved organic matter did not differ across the range of pCO2 conditions tested. In particular, the ratio for particulate organic C and N was found to be 6.58 ± 0.05, close to the theoretical value of 6.6.

High pCO 2-induced exopolysaccharide-rich ballasted aggregates of planktonic cyanobacteria could explain Paleoproterozoic carbon burial

DOE PAGES

Kamennaya, Nina A.; Zemla, Marcin; Mahoney, Laura; ...

2018-05-29

Here, the contribution of planktonic cyanobacteria to burial of organic carbon in deep-sea sediments before the emergence of eukaryotic predators ~1.5 Ga has been considered negligible owing to the slow sinking speed of their small cells. However, global, highly positive excursion in carbon isotope values of inorganic carbonates ~2.22–2.06 Ga implies massive organic matter burial that had to be linked to oceanic cyanobacteria. Here to elucidate that link, we experiment with unicellular planktonic cyanobacteria acclimated to high partial CO 2 pressure ( pCO 2) representative of the early Paleoproterozoic. We find that high pCO 2 boosts generation of acidic extracellularmore » polysaccharides (EPS) that adsorb Ca and Mg cations, support mineralization, and aggregate cells to form ballasted particles. The down flux of such self-assembled cyanobacterial aggregates would decouple the oxygenic photosynthesis from oxidative respiration at the ocean scale, drive export of organic matter from surface to deep ocean and sustain oxygenation of the planetary surface.« less

High pCO 2-induced exopolysaccharide-rich ballasted aggregates of planktonic cyanobacteria could explain Paleoproterozoic carbon burial

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kamennaya, Nina A.; Zemla, Marcin; Mahoney, Laura

Here, the contribution of planktonic cyanobacteria to burial of organic carbon in deep-sea sediments before the emergence of eukaryotic predators ~1.5 Ga has been considered negligible owing to the slow sinking speed of their small cells. However, global, highly positive excursion in carbon isotope values of inorganic carbonates ~2.22–2.06 Ga implies massive organic matter burial that had to be linked to oceanic cyanobacteria. Here to elucidate that link, we experiment with unicellular planktonic cyanobacteria acclimated to high partial CO 2 pressure ( pCO 2) representative of the early Paleoproterozoic. We find that high pCO 2 boosts generation of acidic extracellularmore » polysaccharides (EPS) that adsorb Ca and Mg cations, support mineralization, and aggregate cells to form ballasted particles. The down flux of such self-assembled cyanobacterial aggregates would decouple the oxygenic photosynthesis from oxidative respiration at the ocean scale, drive export of organic matter from surface to deep ocean and sustain oxygenation of the planetary surface.« less

The Carbon Isotopic Composition of Organic Matter in the Microfossils of Planktonic Foraminifera

NASA Astrophysics Data System (ADS)

Swart, K. A.; Oleynik, S.; Sigman, D. M.

2016-12-01

Surface ocean pCO2 is an important measure of the ocean/atmosphere C cycle. Reconstruction of euphotic zone pCO2 over glacial cycles has the potential to indicate the roles of different ocean regions in atmospheric pCO2 changes. Moreover, pCO2 in some surface ocean regions should provide a measure of atmospheric pCO2 change over periods predating the ice core record. The δ13C values of phytoplankton biomass have been used as a proxy for surface ocean pCO2, although carbon fixation rate and other parameters are also important. We have investigated "foraminifera-bound organic matter" (FBOM) as an alternative to bulk sedimentary organic matter for δ13C measurement. One motivation is the ubiquity of foraminifera in unproductive regions where conditions are best for reconstruction of pCO2 but where sedimentary organic matter concentrations are low. We have modified an elemental analyzer so that, interfaced with a stable isotope ratio mass spectrometer, precision for δ13C is 0.2‰ down to 20 nmol C, 1500-fold less C than typically required. This allows for measurements of 10 tests. Cleaning and decalcification protocols have been developed for the analysis of FBOM δ13C (1SD = .4‰). In Holocene sediments from the tropical N. Atlantic, FBOM C content is 65-95 µm C/g CaCO3, with a C/N of 20. For G. ruber, the Holocene δ13C value is -25.0±0.4‰, 2-3‰ lower than surface water suspended POM and expected photosynthate. This difference, along with the high C/N, suggests that FBOM has a substantial lipid component. G. ruber and G. sacculifer, which share similar ecological niches, δ13C values and downcore trends are similar. We do not see systemic differences among species in Holocene sediments that relate to depth of habitat or the presence of endosymbionts. We have examined three tropical N. Atlantic sediment cores back to the last ice age. Given ice core information on pCO2 and reconstruction of local SST, FBOM δ13C values in G. ruber from one core show the expected amplitude of δ13C elevation during the LGM, while 2 other records do not show this shift, with instead a slightly lower FBOM δ13C value during the LGM. Possible explanations for these findings will be offered. Moreover, measurements will be reported on coretop samples from the equatorial Pacific.

Predicting the Response of Molluscs to the Impact of Ocean Acidification

PubMed Central

Parker, Laura M.; Ross, Pauline M.; O’Connor, Wayne A.; Pörtner, Hans O.; Scanes, Elliot; Wright, John M.

2013-01-01

Elevations in atmospheric carbon dioxide (CO2) are anticipated to acidify oceans because of fundamental changes in ocean chemistry created by CO2 absorption from the atmosphere. Over the next century, these elevated concentrations of atmospheric CO2 are expected to result in a reduction of the surface ocean waters from 8.1 to 7.7 units as well as a reduction in carbonate ion (CO32−) concentration. The potential impact that this change in ocean chemistry will have on marine and estuarine organisms and ecosystems is a growing concern for scientists worldwide. While species-specific responses to ocean acidification are widespread across a number of marine taxa, molluscs are one animal phylum with many species which are particularly vulnerable across a number of life-history stages. Molluscs make up the second largest animal phylum on earth with 30,000 species and are a major producer of CaCO3. Molluscs also provide essential ecosystem services including habitat structure and food for benthic organisms (i.e., mussel and oyster beds), purification of water through filtration and are economically valuable. Even sub lethal impacts on molluscs due to climate changed oceans will have serious consequences for global protein sources and marine ecosystems. PMID:24832802

Carbon speciation at the air-sea interface during rain

NASA Astrophysics Data System (ADS)

McGillis, Wade; Hsueh, Diana; Takeshita, Yui; Donham, Emily; Markowitz, Michele; Turk, Daniela; Martz, Todd; Price, Nicole; Langdon, Chris; Najjar, Raymond; Herrmann, Maria; Sutton, Adrienne; Loose, Brice; Paine, Julia; Zappa, Christopher

2015-04-01

This investigation demonstrates the surface ocean dilution during rain events on the ocean and quantifies the lowering of surface pCO2 affecting the air-sea exchange of carbon dioxide. Surface salinity was measured during rain events in Puerto Rico, the Florida Keys, East Coast USA, Panama, and the Palmyra Atoll. End-member analysis is used to determine the subsequent surface ocean carbonate speciation. Surface ocean carbonate chemistry was measured during rain events to verify any approximations made. The physical processes during rain (cold, fresh water intrusion and buoyancy, surface waves and shear, microscale mixing) are described. The role of rain on surface mixing, biogeochemistry, and air-sea gas exchange will be discussed.

Physical state of the very early Earth

NASA Astrophysics Data System (ADS)

Abe, Yutaka

1993-09-01

The earliest surface environment of the Earth is reconstructed in accordance with the planetary formation theory. Formation of an atmosphere is an inevitable consequence of Earth's formation. The atmosphere near the close of accretion is composed of 200 ˜ 300 bars of H 2 and H 2O, and several tens of bars of CO and CO 2. Either by the blanketing effect of the proto-atmosphere or heating by large planetesimal impacts a magma ocean is formed during accretion. We can distinguish three stages for the thermal evolution of the magma ocean and proto-crust. Stage 0 is characterized by a super-liquidus (or completely molten) regime near the surface. At this stage the surface of the Earth is covered by a super-liquidus magma ocean. No chemical differentiation is expected during this stage. Once the energy flux released by planet formation decreases to the 200 W/m 2 level the super-liquidus magma ocean then disappears within a time interval of 1 m.y. This is the transition from stage 0 to 1. Stage 1 is characterized by a partially molten magma ocean. In the magma ocean consisting of 20 ˜ 30% partial melt, heat transport is controlled by melt-solid separation (a type of compositional convection) rather than thermal convection. Chemical differentiation of the mantle mainly occurs in this stage. Once the energy flux drops to the 160 W/m 2 level, more than 90% of water vapor in the proto-atmosphere condense to form the proto-oceans. Several tens of bars of CO and CO 2 remain in the atmosphere just after formation of the oceans. Water oceans are occasionally evaporated by large impacts. After each such event, recondensation of the ocean takes several hundred years. Although the surface is covered by a chilled proto-crust, it is short-lived because of extensive volcanic resurfacing activity as well as meteorite impacts resurfacing. This stage ends when the energy flux drops to 0.1 ˜ 1 W/m 2 level. The duration time of stage 1 is estimated to be several hundred million years (the best estimate is about 400 m.y.). Stage 2 is characterized by solid state convection. This stage continues to the present day. One of the most important change on the proto-Earth is the transition from stage 1 to 2, which occurs several hundred million years after the Earth formation. Long-lived crust is formed only after this transition.

Effects of acute ocean acidification on spatially-diverse polar pelagic foodwebs: Insights from on-deck microcosms

NASA Astrophysics Data System (ADS)

Tarling, G. A.; Peck, V. L.; Ward, P.; Ensor, N. S.; Achterberg, E.; Tynan, E.; Poulton, A. J.; Mitchell, E.; Zubkov, M. V.

2016-05-01

The polar oceans are experiencing some of the largest levels of ocean acidification (OA) resulting from the uptake of anthropogenic carbon dioxide (CO2). Our understanding of the impacts this is having on polar marine communities is mainly derived from studies of single species in laboratory conditions, while the consequences for food web interactions remain largely unknown. This study carried out experimental manipulations of natural pelagic communities at different high latitude sites in both the northern (Nordic Seas) and southern hemispheres (Scotia and Weddell Seas). The aim of this study was to identify more generic responses and achieve greater experimental reproducibility through implementing a series of short term (4 d), multilevel (3 treatment) carbonate chemistry manipulation experiments on unfiltered natural surface-ocean communities, including grazing copepods. The experiments were successfully executed at six different sites, covering a diverse range of environmental conditions and differing plankton community compositions. The study identified the interaction between copepods and dinoflagellate cell abundance to be significantly altered by elevated levels of dissolved CO2 (pCO2), with dinoflagellates decreasing relative to ambient conditions across all six experiments. A similar pattern was not observed in any other major phytoplankton group. The patterns indicate that copepods show a stronger preference for dinoflagellates when in elevated pCO2 conditions, demonstrating that changes in food quality and altered grazing selectivity may be a major consequence of ocean acidification. The study also found that transparent exopolymeric particles (TEP) generally increased when pCO2 levels were elevated, but the response was dependent on the exact set of environmental conditions. Bacteria and nannoplankton showed a neutral response to elevated pCO2 and there was no significant relationship between changes in bacterial or nannoplankton abundance and that of TEP concentrations. Overall, the study illustrated that, although some similar responses exist, these contrasting high latitude surface ocean communities are likely to show different responses to the onset of elevated pCO2.

Propagation of vent CO2 in a subtropical shallow-water ecosystem assessed by stable carbon isotopes

NASA Astrophysics Data System (ADS)

Cheng, Y. F.; Chen, C. T. A.; Liao, Y. M.; Lin, Y. S.

2016-02-01

Carbon cycle of the ocean plays an important role in the global change associated with the emission of CO2. Anthropogenic CO2 dissolves in seawater, changes carbon chemistry of the ocean, and affects marine life in different and complicated ways. In this study, we investigated stable carbon isotope systematics of a shallow-water hydrothermal field near the Kueishantao Islet off NE Taiwan, which has vent gas composition dominated by CO2 and world record breaking low pH hydrothermal fluids. By studying this natural laboratory of ocean acidification, we aim at clarifying to which extent the high dosage of CO2 propagates in the subtropical shallow-water ecosystem, and how it affects the carbon cycle. Samples of seawater and suspended particles were collected from stations of two nearshore-offshore transects, one with hydrothermal vents at the nearshore end (Transect M, 1230 m long) and the other serving as the baseline (Transect B, 1560 m long). Surface seawater of Transect M showed increasing pH in the offshore direction, from 5.8 at the vent mouths to 7.6 at the most distant station. In contrast, pH of surface water decreased seaward from 8.0 to 7.8 in Transect B. The δ13C values of the vent CO2 averaged -6.4‰, consistent with the range attributed to mantle CO2. Seawater DIC δ13C values of Transect M were 13C-depleted (as negative as -2.5‰) at the vent mouths, and became increasingly 13C-enriched till 0.7‰ at the most distant station. This pattern is in clear contrast to that of Transect B, the DIC δ13C values of which decreased from 0.7 to 0.6 ‰ in the offshore direction. We concluded that the vent CO2 has propagated in the surface ocean at least >700 m away from the hydrothermal field. Our next step is to explore how the vent CO2 affects the stable carbon isotopes of particulate organic matter, and to assess the effect of vent CO2 using quantitative approaches.

Effects of Water Amount on the Surface Environment of Terrestrial Planets: High Pressure Ice and Carbon Cycle

NASA Astrophysics Data System (ADS)

Nakayama, Akifumi; Abe, Yutaka

2015-12-01

Terrestrial planets with several wt% of H2O in extrasolar planetary systems are theoretically predicted in the habitable zone [Raymond et al., 2004]. Such planets are expected to be covered by an ocean entirely (called as “ocean planets”). Amount of atmospheric CO2 (PCO2) is important for surface environment because CO2 is a strong greenhouse gas. PCO2 is determined by a race between degassing and sink through weathering on carbon cycle. On an ocean planet, seafloor weathering is important because continental weathering can’t work [Abbot et al., 2012]. In addition, ocean planets with large water amount may have high-pressure (HP) ice on the seafloor [Leger et al., 2004]. Since the ocean floor is covered by ice in such case, it has been thought that any weathering processes will not work and PCO2 will be extremely high. When plate tectonics works, heat flow from oceanic crust decreases with distance from the mid ocean ridge. Therefore, HP ice near the mid ocean ridge will be kept solid-liquid coexistent state at the melting point because of high heat flow. Seafloor weathering works in this region. The seafloor weathering under this condition efficiently works because weathering temperature is kept melting point regardless of surface temperature. Thus, our aim is to clarify the relationship between water amount and surface environment focusing seafloor environment. We develop a carbon cycle model considering the seafloor weathering. Our major assumptions are following; 1) Earth-sized ocean planets with various water amount, 2) Degassing rate is depended on the total amount of carbon and total carbon inventory is proportional to the surface water amount. We investigated thermal state of HP ice and determined effective weathering region where HP ice is coexistent with water, then we investigated the PCO2 in equilibrium state where degassing and regassing are balanced. As a result, forming of HP ice may cause snowball state due to high weathering rate. When solar incident flux and heat flow from mantle are the present Earth’s value and a ratio of CO2 / H2O inventory is carbonaceous chondrite composition, a planet with large ocean which is larger than 90 Earth’s ocean mass lapses into snowball state. It was previously believed that forming of HP ice supports warm climate; rather, forming of HP ice could cause snowball state.

Multidecadal fCO2 Increase Along the United States Southeast Coastal Margin

NASA Astrophysics Data System (ADS)

Reimer, Janet J.; Wang, Hongjie; Vargas, Rodrigo; Cai, Wei-Jun

2017-12-01

Coastal margins could be hotspots for acidification due to terrestrial-influenced CO2 sources. Currently there are no long-term (>20 years) records from biologically important coastal environments that could demonstrate sea surface CO2 fugacity (fCO2) and pH trends. Here, multidecadal fCO2 trends are calculated from underway and moored time series observations along the United States southeast coastal margin, also referred to as the South Atlantic Bight (SAB). fCO2 trends across the SAB, derived from ˜26 years of cruises and ˜9.5 years from a moored time series, range from 3.0 to 4.5 µatm yr-1, and are greater than the open ocean increases. The pH decline related to the fCO2 increases could be as much as -0.004 yr-1; a rate greater than that expected from atmospheric-influenced pH alone. We provide evidence that fCO2 increases and pH decreases on an ocean margin can be faster than those predicted for the open ocean from atmospheric influence alone. We conclude that a substantial fCO2 increase across the marginal SAB is due to both increasing temperature on the middle and outer shelves, but to lateral land-ocean interactions in the coastal zone and on inner shelf.

The relative influence of H2O and CO2 on the primitive surface conditions of Venus

NASA Astrophysics Data System (ADS)

Salvador, A.; Massol, H.; Davaille, A.; Marcq, E.; Sarda, P.; Chassefiere, E.

2017-12-01

How the volatile content influences the primordial surface conditions of terrestrial planets and, thus, their future geodynamic evolution is an important question to answer. We simulate the secular convective cooling of a 1-D magma ocean (MO) in interaction with its outgassed atmosphere. A first rapid cooling stage, where efficient MO cooling and degassing take place, producing the atmosphere, is followed by a second quasi steady state where the heat flux balance is dominated by the solar flux. The end ofthe rapid cooling stage (ERCS) is reached when the mantle heat flux becomes negligible compared tothe absorbed solar flux. Varying the initial CO2 and H2O contents and the solar distance, we showed that the resulting surface conditions at ERCS strongly depend on these parameters and that water ocean's formation obeys simple scaling laws.Although today's Venus is located beyond the inner edge of the habitable zone due to its high albedo, its high CO2/H2O ratio prevents any water ocean formation.We already showed that depending on the formation time of its cloudcover and resulting albedo, only 0.3 Earth ocean mass might be sufficient to form a water ocean onearly Venus. Here we investigate more precisely these results by taking into account the effect of shortwave radiation on the radiative budget by computing the feedbacks between atmospheric composition and incident stellar flux instead of using a prescribed albedo value.

Re-evaluating the 1940s CO2 plateau

NASA Astrophysics Data System (ADS)

Bastos, A.; Ciais, P.; Barichivitch, J.; Brovkin, V.; Gasser, T.; Pongratz, J.; Trudinger, C. M.

2016-12-01

The ice-core record reveals a stabilisation of atmospheric CO2 in the 1940s (the so called "plateau"), in spite of continued emissions from fossil fuel burning (FF) and land-use change (LUC). This stabilisation has been previously attributed to very strong oceanic CO2 uptake, perhaps in response to the El-Niño event in 1940. However, this explanation is questionable, since recent atmospheric CO2 data indicate that El Niño events generally lead to higher atmospheric CO2 growth-rates because of the terrestrial response, and oceanic CO2 measurements indicate the range of variability in the ocean sink has been rather modest in recent decades. We use up-to-date reconstructions of the CO2 sources (FF and LUC), ocean uptake from two different reconstructions and the terrestrial sink (from TRENDY models) over the 20th century to evaluate whether these allow capturing the CO2 plateau and provide further insight about its drivers. While these datasets provide a plausible explanation for most of the 20th century carbon budget, especially since 1970, they overestimate atmospheric CO2 growth rate during the plateau period by 0.9-2.0PgC.yr-1. We test the possible explanations for this mismatch, namely i) the role of natural variability in the ocean sink; ii) the representation of the terrestrial sink response to the climate anomalies during the 1940s by land-surface models; iii) the contribution of land-use processes possibly not represented in the current datasets. We conclude that a strong terrestrial sink concurrent with enhanced oceanic uptake is required to explain the CO2 stabilisation. Tests performed using the OSCAR carbon-cycle model suggest that changes in land-use coinciding with drastic socioeconomic changes during WW2 could plausibly contribute to the additional sink required.

Airborne Two-Micron Double-Pulse IPDA Lidar Validation for Carbon Dioxide Measurements Over Land

NASA Astrophysics Data System (ADS)

Refaat, Tamer F.; Singh, Upendra N.; Yu, Jirong; Petros, Mulugeta; Remus, Ruben; Ismail, Syed

2018-04-01

An airborne double-pulse 2-μm Integrated Path Differential Absorption (IPDA) lidar has been developed at NASA LaRC for measuring atmospheric CO2. IPDA was validated using NASA B-200 aircraft over land and ocean under different conditions. IPDA evaluation for land vegetation returns, during full day background conditions, are presented. IPDA CO2 measurements compare well with model results driven from on-board insitu sensor data. These results also indicate that CO2 measurement bias is consistent with that from ocean surface returns.

Deep-sea coral evidence for lower Southern Ocean surface nitrate concentrations during the last ice age

NASA Astrophysics Data System (ADS)

Wang, Xingchen Tony; Sigman, Daniel M.; Prokopenko, Maria G.; Adkins, Jess F.; Robinson, Laura F.; Hines, Sophia K.; Chai, Junyi; Studer, Anja S.; Martínez-García, Alfredo; Chen, Tianyu; Haug, Gerald H.

2017-03-01

The Southern Ocean regulates the ocean’s biological sequestration of CO2 and is widely suspected to underpin much of the ice age decline in atmospheric CO2 concentration, but the specific changes in the region are debated. Although more complete drawdown of surface nutrients by phytoplankton during the ice ages is supported by some sediment core-based measurements, the use of different proxies in different regions has precluded a unified view of Southern Ocean biogeochemical change. Here, we report measurements of the 15N/14N of fossil-bound organic matter in the stony deep-sea coral Desmophyllum dianthus, a tool for reconstructing surface ocean nutrient conditions. The central robust observation is of higher 15N/14N across the Southern Ocean during the Last Glacial Maximum (LGM), 18-25 thousand years ago. These data suggest a reduced summer surface nitrate concentration in both the Antarctic and Subantarctic Zones during the LGM, with little surface nitrate transport between them. After the ice age, the increase in Antarctic surface nitrate occurred through the deglaciation and continued in the Holocene. The rise in Subantarctic surface nitrate appears to have had both early deglacial and late deglacial/Holocene components, preliminarily attributed to the end of Subantarctic iron fertilization and increasing nitrate input from the surface Antarctic Zone, respectively.

Deep-sea coral evidence for lower Southern Ocean surface nitrate concentrations during the last ice age

PubMed Central

Sigman, Daniel M.; Prokopenko, Maria G.; Adkins, Jess F.; Robinson, Laura F.; Hines, Sophia K.; Chai, Junyi; Studer, Anja S.; Martínez-García, Alfredo; Chen, Tianyu; Haug, Gerald H.

2017-01-01

The Southern Ocean regulates the ocean’s biological sequestration of CO2 and is widely suspected to underpin much of the ice age decline in atmospheric CO2 concentration, but the specific changes in the region are debated. Although more complete drawdown of surface nutrients by phytoplankton during the ice ages is supported by some sediment core-based measurements, the use of different proxies in different regions has precluded a unified view of Southern Ocean biogeochemical change. Here, we report measurements of the 15N/14N of fossil-bound organic matter in the stony deep-sea coral Desmophyllum dianthus, a tool for reconstructing surface ocean nutrient conditions. The central robust observation is of higher 15N/14N across the Southern Ocean during the Last Glacial Maximum (LGM), 18–25 thousand years ago. These data suggest a reduced summer surface nitrate concentration in both the Antarctic and Subantarctic Zones during the LGM, with little surface nitrate transport between them. After the ice age, the increase in Antarctic surface nitrate occurred through the deglaciation and continued in the Holocene. The rise in Subantarctic surface nitrate appears to have had both early deglacial and late deglacial/Holocene components, preliminarily attributed to the end of Subantarctic iron fertilization and increasing nitrate input from the surface Antarctic Zone, respectively. PMID:28298529

Reduction in Surface Ocean Carbon Storage across the Middle Miocene

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Insights into Ocean Acidification During the Middle Eocene Climatic Optimum from Boron Isotopes at Southern Ocean Site 738

NASA Astrophysics Data System (ADS)

Moebius, I.; Hoenisch, B.; Friedrich, O.

2015-12-01

The Middle Eocene Climatic Optimum (MECO) is a ~650-kyr interval of global warming, with a brief ~50 ky long peak warming interval, and an abrupt termination. Deep sea and surface ocean temperature evolution across this interval are fairly well constrained, but thus far we have little understanding of the mechanisms responsible for the gradual warming and rapid recovery. Carbonate mass accumulation rates suggest a shoaling of the carbonate compensation depth, and studies on alkenones indicate increasing atmospheric CO2 levels during the MECO. This suggests an increase in surface ocean CO2, and consequently ocean acidification. However, the severity and timing of the proposed ocean acidification with respect to the onset, peak warming and the termination are currently not well resolved. The boron isotopic composition (δ11B) recorded in planktic foraminifer shells offers an opportunity to infer oceanic pH across this interval. We are working on a boron isotope reconstruction from Southern Ocean IODP site 738 and South Atlantic IODP site 1263, covering 42.0 to 38.5 Ma. These sites are characterized by good carbonate preservation and well-defined age models have been established. Additionally, ecology, nutrient content and bottom-water oxygenation have been shown to change significantly across the event towards a more eutrophic, periodically oxygen-depleted environment supporting different biological communities. We selected the planktic foraminifera species Acarinina spinuloinflata for this study because it is symbiont-bearing, suggesting a near-surface habitat and little vertical migration in the water column, and because of its abundance in the samples. δ11B data will be translated to surface ocean pH and atmospheric pCO2 will be approximated to refine knowledge about the carbon cycle during this time. Parallel analysis of two core sites will help to evaluate the tenacity of the data.

On the calculation of air-sea fluxes of CO2 in the presence of temperature and salinity gradients

NASA Astrophysics Data System (ADS)

Woolf, D. K.; Land, P. E.; Shutler, J. D.; Goddijn-Murphy, L. M.; Donlon, C. J.

2016-02-01

The presence of vertical temperature and salinity gradients in the upper ocean and the occurrence of variations in temperature and salinity on time scales from hours to many years complicate the calculation of the flux of carbon dioxide (CO2) across the sea surface. Temperature and salinity affect the interfacial concentration of aqueous CO2 primarily through their effect on solubility with lesser effects related to saturated vapor pressure and the relationship between fugacity and partial pressure. The effects of temperature and salinity profiles in the water column and changes in the aqueous concentration act primarily through the partitioning of the carbonate system. Climatological calculations of flux require attention to variability in the upper ocean and to the limited validity of assuming "constant chemistry" in transforming measurements to climatological values. Contrary to some recent analysis, it is shown that the effect on CO2 fluxes of a cool skin on the sea surface is large and ubiquitous. An opposing effect on calculated fluxes is related to the occurrence of warm layers near the surface; this effect can be locally large but will usually coincide with periods of low exchange. A salty skin and salinity anomalies in the upper ocean also affect CO2 flux calculations, though these haline effects are generally weaker than the thermal effects.

The relative influence of H2O and CO2 on the primitive surface conditions and evolution of rocky planets

NASA Astrophysics Data System (ADS)

Salvador, A.; Massol, H.; Davaille, A.; Marcq, E.; Sarda, P.; Chassefière, E.

2017-07-01

How the volatile content influences the primordial surface conditions of terrestrial planets and, thus, their future geodynamic evolution is an important question to answer. We simulate the secular convective cooling of a 1-D magma ocean (MO) in interaction with its outgassed atmosphere. The heat transfer in the atmosphere is computed either using the grey approximation or using a k-correlated method. We vary the initial CO2 and H2O contents (respectively from 0.1 × 10-2 to 14 × 10-2 wt % and from 0.03 to 1.4 times the Earth Ocean current mass) and the solar distance—from 0.63 to 1.30 AU. A first rapid cooling stage, where efficient MO cooling and degassing take place, producing the atmosphere, is followed by a second quasi steady state where the heat flux balance is dominated by the solar flux. The end of the rapid cooling stage (ERCS) is reached when the mantle heat flux becomes negligible compared to the absorbed solar flux. The resulting surface conditions at ERCS, including water ocean's formation, strongly depend both on the initial volatile content and solar distance D. For D > DC, the "critical distance," the volatile content controls water condensation and a new scaling law is derived for the water condensation limit. Although today's Venus is located beyond DC due to its high albedo, its high CO2/H2O ratio prevents any water ocean formation. Depending on the formation time of its cloud cover and resulting albedo, only 0.3 Earth ocean mass might be sufficient to form a water ocean on early Venus.

Fast Atmosphere-Ocean Model Runs with Large Changes in CO2

NASA Technical Reports Server (NTRS)

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

2013-01-01

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

Iron Resources and Oceanic Nutrients - Advancement of Global Environment Simulations (ironages)

NASA Astrophysics Data System (ADS)

de Baar, H. J. W.; Ironages Team

Iron limits productivity in 40 percent of the oceans, and is a co-limitation in the re- maining 60 percent of surface waters. Moreover the paradigm of a single factor limit- ing plankton blooms, is presently giving way to co-limitation by light, and the nutri- ents N, P, Si, and Fe. Primary production, export into the deep sea, and CO2 uptake from the atmosphere together form the 'biological pump' in Ocean Biogeochemi- cal Climate Models (OBCM's). Thus far OBCM's assume just one limiting nutrient (P) and one universal phytoplankton species, for deriving C budgets and CO2 ex- change with the atmosphere. New realistic OBCM's are being developed in IRON- AGES for budgeting and air/sea exchanges of both CO2 and DMS, implementing (1) co-limitation by 4 nutrients of 5 major taxonomic classes of phytoplankton in a nested plankton ecosystem model, (ii) DMS(P) pathways, (iii) global iron cycling, (iv) chem- ical forms of iron and (v) iron supply in surface waters from above by aerosols and from below out of reducing margin sediments. IRONAGES is a consortium of 12 Eu- ropean institutes coordinated by the Royal NIOZ.

Ocean Carbon Cycle Feedbacks Under Negative Emissions

NASA Astrophysics Data System (ADS)

Schwinger, Jörg; Tjiputra, Jerry

2018-05-01

Negative emissions will most likely be needed to achieve ambitious climate targets, such as limiting global warming to 1.5°. Here we analyze the ocean carbon-concentration and carbon-climate feedback in an Earth system model under an idealized strong CO2 peak and decline scenario. We find that the ocean carbon-climate feedback is not reversible by means of negative emissions on decadal to centennial timescales. When preindustrial surface climate is restored, the oceans, due to the carbon-climate feedback, still contain about 110 Pg less carbon compared to a simulation without climate change. This result is unsurprising but highlights an issue with a widely used carbon cycle feedback metric. We show that this metric can be greatly improved by using ocean potential temperature as a proxy for climate change. The nonlinearity (nonadditivity) of climate and CO2-driven feedbacks continues to grow after the atmospheric CO2 peak.

Surface Water pCO2 Variations and Sea-Air CO2 Fluxes During Summer in the Eastern Canadian Arctic

NASA Astrophysics Data System (ADS)

Burgers, T. M.; Miller, L. A.; Thomas, H.; Else, B. G. T.; Gosselin, M.; Papakyriakou, T.

2017-12-01

Based on a 2 year data set, the eastern Canadian Arctic Archipelago and Baffin Bay appear to be a modest summertime sink of atmospheric CO2. We measured surface water CO2 partial pressure (pCO2), salinity, and temperature throughout northern Baffin Bay, Nares Strait, and Lancaster Sound from the CCGS Amundsen during its 2013 and 2014 summer cruises. Surface water pCO2 displayed considerable variability (144-364 μatm) but never exceeded atmospheric concentrations, and average calculated CO2 fluxes in 2013 and 2014 were -12 and -3 mmol C m-2 d-1 (into the ocean), respectively. Ancillary measurements of chlorophyll a reveal low summertime productivity in surface waters. Based on total alkalinity and stable oxygen isotopes (δ18O) data, a strong riverine signal in northern Nares Strait coincided with relatively high surface pCO2, whereas areas of sea-ice melt occur with low surface pCO2. Further assessments, extending the seasonal observation period, are needed to properly constrain both seasonal and annual CO2 fluxes in this region.

The Southern Ocean biogeochemical divide.

PubMed

Marinov, I; Gnanadesikan, A; Toggweiler, J R; Sarmiento, J L

2006-06-22

Modelling studies have demonstrated that the nutrient and carbon cycles in the Southern Ocean play a central role in setting the air-sea balance of CO(2) and global biological production. Box model studies first pointed out that an increase in nutrient utilization in the high latitudes results in a strong decrease in the atmospheric carbon dioxide partial pressure (pCO2). This early research led to two important ideas: high latitude regions are more important in determining atmospheric pCO2 than low latitudes, despite their much smaller area, and nutrient utilization and atmospheric pCO2 are tightly linked. Subsequent general circulation model simulations show that the Southern Ocean is the most important high latitude region in controlling pre-industrial atmospheric CO(2) because it serves as a lid to a larger volume of the deep ocean. Other studies point out the crucial role of the Southern Ocean in the uptake and storage of anthropogenic carbon dioxide and in controlling global biological production. Here we probe the system to determine whether certain regions of the Southern Ocean are more critical than others for air-sea CO(2) balance and the biological export production, by increasing surface nutrient drawdown in an ocean general circulation model. We demonstrate that atmospheric CO(2) and global biological export production are controlled by different regions of the Southern Ocean. The air-sea balance of carbon dioxide is controlled mainly by the biological pump and circulation in the Antarctic deep-water formation region, whereas global export production is controlled mainly by the biological pump and circulation in the Subantarctic intermediate and mode water formation region. The existence of this biogeochemical divide separating the Antarctic from the Subantarctic suggests that it may be possible for climate change or human intervention to modify one of these without greatly altering the other.

A hybrid model of the CO2 geochemical cycle and its application to large impact events

NASA Technical Reports Server (NTRS)

Kasting, J. F.; Pollack, J. B.; Toon, O. B.; Richardson, S. M.

1986-01-01

The effects of a large asteriod or comet impact on modern and ancient marine biospheres are analyzed. A hybrid model of the carbonate-silicate geochemical cycle, which is capable of calculating the concentrations of carbon dioxide in the atmosphere, ocean, and sedimentary rocks, is described. The differences between the Keir and Berger (1983) model and the hybrid model are discussed. Equilibrium solutions are derived for the preindustrial atmosphere/ocean system and for a system similar to that of the late Cretaceous Period. The model data reveal that globl darkening caused by a stratospheric dust veil could destroy the existing phytoplankton within a period of several weeks or months, nd the dissolution of atmospheric NO(x) compounds would lower the pH of ocean surface waters and release CO2 into the atmosphere. It is noted that the surface temperatures could be increased by several degrees and surface oceans would be uninhabitable for calcaerous organisms for approximately 20 years.

Vertical observation of molecular hydrogen and carbon monoxide: Implication for non-photochemical H2 production at ocean surface and subsurface

NASA Astrophysics Data System (ADS)

Kawagucci, S.; Narita, T.; Obata, H.; Ogawa, H.; Gamo, T.

2009-12-01

Biological nitrogen fixation is a key metabolism controlling marine N-cycling and also known as a main H2 source. Recently, it was proposed that a monitoring of surface H2 concentration could be used quickly to figure out the spatial extent of biological nitrogen fixation activity without onboard incubation required for currently used methods for detecting the activity. However, H2 behavior in ocean water was still unresolved. This study carried out vertical observation of H2 and CO concentrations in south of Japan, western North Pacific. Because carbon monoxide, CO, in seawater has no relation with nitrogen fixation metabolism and is produced dominantly by the photochemical reaction, which is an altanative H2 source, simultaneous observation and comparison of H2 and CO concentration is helpful to investigate H2 behavior in ocean water. Reductive gases in seawater were observed during the R/V Tansei-maru KT-08-14 cruise by using a wired CTD-CMS (CTD-carousel multiple sampling) system to conduct vertical sampling (at most 200 m depth) and by using a plastic bucket for sampling surface seawater. The sample in the Niskin-X bottle was directed to the bottom of a 120 mL brown-colored glass vial allowed to overflow by 2 volumes before the tube was slowly withdrawn. After the addition of 0.5 mL HgCl2-saturated solution for poisoning, the PTFE-lined butyl-gum septum was used to cap the vials. Molecular hydrogen (H2) and carbon monoxide (CO) were analyzed at an onboard laboratory within 6 hours after subsampling. 20 mL of sample water was substituted by 20 mL of H2- and CO-free air using a gas-tight syringe; then the vial was put on an automatic shaker and shaken upside down for 6 minutes to achieve a complete equilibrium between the dissolved and head space gases in the vial. The equilibrated headspace was taken by another gas-tight syringe and then injected into a gas chromatograph equipped with a trace reduced gas detector. Vertical distribution of dissolved H2 and CO concentration were observed. Apparently different vertical distributions between H2 and CO concentration were revealed at all the observed stations. At a station where N-nutrient was depleted through surface mixed layer, H2 was supersaturated at the surface while CO concentration was constant through the depths. In contrast, at another station where some amount of terrestrial humic matter was introduced into the surface, H2 concentration was constantly undersaturated through the depth while vertical distribution of CO concentration showed the highest at the surface and exponentially decreased to deep. These facts suggest that H2 production involved with nitrogen fixation played an important role for H2 behavior in ocean water while photochemical H2 production would be a minor process. In addition to the surface, H2 supersaturation accoumpanied with little CO concentration rise were observed at depths just below the mixed layer in pycnocline with Chlorophyll maximum.

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

NASA Astrophysics Data System (ADS)

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 useful for improving the partitioning between ocean and land sinks and the spatial distribution of the inverted carbon flux.

The spatial and interannual dynamics of the surface water carbonate system and air-sea CO2 fluxes in the outer shelf and slope of the Eurasian Arctic Ocean

NASA Astrophysics Data System (ADS)

Pipko, Irina I.; Pugach, Svetlana P.; Semiletov, Igor P.; Anderson, Leif G.; Shakhova, Natalia E.; Gustafsson, Örjan; Repina, Irina A.; Spivak, Eduard A.; Charkin, Alexander N.; Salyuk, Anatoly N.; Shcherbakova, Kseniia P.; Panova, Elena V.; Dudarev, Oleg V.

2017-11-01

The Arctic is undergoing dramatic changes which cover the entire range of natural processes, from extreme increases in the temperatures of air, soil, and water, to changes in the cryosphere, the biodiversity of Arctic waters, and land vegetation. Small changes in the largest marine carbon pool, the dissolved inorganic carbon pool, can have a profound impact on the carbon dioxide (CO2) flux between the ocean and the atmosphere, and the feedback of this flux to climate. Knowledge of relevant processes in the Arctic seas improves the evaluation and projection of carbon cycle dynamics under current conditions of rapid climate change. Investigation of the CO2 system in the outer shelf and continental slope waters of the Eurasian Arctic seas (the Barents, Kara, Laptev, and East Siberian seas) during 2006, 2007, and 2009 revealed a general trend in the surface water partial pressure of CO2 (pCO2) distribution, which manifested as an increase in pCO2 values eastward. The existence of this trend was defined by different oceanographic and biogeochemical regimes in the western and eastern parts of the study area; the trend is likely increasing due to a combination of factors determined by contemporary change in the Arctic climate, each change in turn evoking a series of synergistic effects. A high-resolution in situ investigation of the carbonate system parameters of the four Arctic seas was carried out in the warm season of 2007; this year was characterized by the next-to-lowest historic sea-ice extent in the Arctic Ocean, on satellite record, to that date. The study showed the different responses of the seawater carbonate system to the environment changes in the western vs. the eastern Eurasian Arctic seas. The large, open, highly productive water area in the northern Barents Sea enhances atmospheric CO2 uptake. In contrast, the uptake of CO2 was strongly weakened in the outer shelf and slope waters of the East Siberian Arctic seas under the 2007 environmental conditions. The surface seawater appears in equilibrium or slightly supersaturated by CO2 relative to atmosphere because of the increasing influence of river runoff and its input of terrestrial organic matter that mineralizes, in combination with the high surface water temperature during sea-ice-free conditions. This investigation shows the importance of processes that vary on small scales, both in time and space, for estimating the air-sea exchange of CO2. It stresses the need for high-resolution coverage of ocean observations as well as time series. Furthermore, time series must include multi-year studies in the dynamic regions of the Arctic Ocean during these times of environmental change.

Ocean Biological Pump Sensitivities and Implications for Climate Change Impacts

NASA Technical Reports Server (NTRS)

Romanou, Anastasia

2013-01-01

The ocean is one of the principal reservoirs of CO2, a greenhouse gas, and therefore plays a crucial role in regulating Earth's climate. Currently, the ocean sequesters about a third of anthropogenic CO2 emissions, mitigating the human impact on climate. At the same time, the deeper ocean represents the largest carbon pool in the Earth System and processes that describe the transfer of carbon from the surface of the ocean to depth are intimately linked to the effectiveness of carbon sequestration.The ocean biological pump (OBP), which involves several biogeochemical processes, is a major pathway for transfer of carbon from the surface mixed layer into the ocean interior. About 75 of the carbon vertical gradient is due to the carbon pump with only 25 attributed to the solubility pump. However, the relative importance and role of the two pumps is poorly constrained. OBP is further divided to the organic carbon pump (soft tissue pump) and the carbonate pump, with the former exporting about 10 times more carbon than the latter through processes like remineralization.Major uncertainties about OBP, and hence in the carbon uptake and sequestration, stem from uncertainties in processes involved in OBP such as particulate organicinorganic carbon sinkingsettling, remineralization, microbial degradation of DOC and uptakegrowth rate changes of the ocean biology. The deep ocean is a major sink of atmospheric CO2 in scales of hundreds to thousands of years, but how the export efficiency (i.e. the fraction of total carbon fixation at the surface that is transported at depth) is affected by climate change remains largely undetermined. These processes affect the ocean chemistry (alkalinity, pH, DIC, particulate and dissolved organic carbon) as well as the ecology (biodiversity, functional groups and their interactions) in the ocean. It is important to have a rigorous, quantitative understanding of the uncertainties involved in the observational measurements, the models and the projections of future changes.

Impacts of artificial ocean alkalinization on the carbon cycle and climate in Earth system simulations

NASA Astrophysics Data System (ADS)

González, Miriam Ferrer; Ilyina, Tatiana

2016-06-01

Using the state-of-the-art emissions-driven Max Planck Institute Earth system model, we explore the impacts of artificial ocean alkalinization (AOA) with a scenario based on the Representative Concentration Pathway (RCP) framework. Addition of 114 Pmol of alkalinity to the surface ocean stabilizes atmospheric CO2 concentration to RCP4.5 levels under RCP8.5 emissions. This scenario removes 940 GtC from the atmosphere and mitigates 1.5 K of global warming within this century. The climate adjusts to the lower CO2 concentration preventing the loss of sea ice and high sea level rise. Seawater pH and the carbonate saturation state (Ω) rise substantially above levels of the current decade. Pronounced differences in regional sensitivities to AOA are projected, with the Arctic Ocean and tropical oceans emerging as hot spots for biogeochemical changes induced by AOA. Thus, the CO2 mitigation potential of AOA comes at a price of an unprecedented ocean biogeochemistry perturbation with unknown ecological consequences.

Acidification of subsurface coastal waters enhanced by eutrophication

EPA Science Inventory

Uptake of fossil-fuel carbon dioxide (CO2) from the atmosphere has acidified the surface ocean by ~0.1 pH units and driven down the carbonate saturation state. Ocean acidification is a threat to marine ecosystems and may alter key biogeochemical cycles. Coastal oceans have also b...

Reduced ventilation and enhanced magnitude of the deep Pacific carbon pool during the last glacial period

NASA Astrophysics Data System (ADS)

Skinner, L.; McCave, I. N.; Carter, L.; Fallon, S.; Scrivner, A. E.; Primeau, F.

2015-02-01

It has been proposed that the ventilation of the deep Pacific carbon pool was not significantly reduced during the last glacial period, posing a problem for canonical theories of glacial-interglacial CO2 change. However, using radiocarbon dates of marine tephra deposited off New Zealand, we show that deep- (> 2000 m) and shallow sub-surface ocean-atmosphere 14C age offsets (i.e. "reservoir-" or "ventilation" ages) in the southwest Pacific increased by ˜1089 and 337 yrs respectively, reaching ˜2689 and ˜1037 yrs during the late glacial. A comparison with other radiocarbon data from the southern high-latitudes suggests that broadly similar changes were experienced right across the Southern Ocean. If, like today, the Southern Ocean was the main source of water to the glacial ocean interior, these observations would imply a significant change in the global radiocarbon inventory during the last glacial period, possibly equivalent to an increase in the average radiocarbon age > 2 km of ˜ 700 yrs. Simple mass balance arguments and numerical model sensitivity tests suggest that such a change in the ocean's mean radiocarbon age would have had a major impact on the marine carbon inventory and atmospheric CO2, possibly accounting for nearly half of the glacial-interglacial CO2 change. If confirmed, these findings would underline the special role of high latitude shallow sub-surface mixing and air-sea gas exchange in regulating atmospheric CO2 during the late Pleistocene.

The polar amplification asymmetry: role of Antarctic surface height

NASA Astrophysics Data System (ADS)

Salzmann, Marc

2017-05-01

Previous studies have attributed an overall weaker (or slower) polar amplification in Antarctica compared to the Arctic to a weaker Antarctic surface albedo feedback and also to more efficient ocean heat uptake in the Southern Ocean in combination with Antarctic ozone depletion. Here, the role of the Antarctic surface height for meridional heat transport and local radiative feedbacks, including the surface albedo feedback, was investigated based on CO2-doubling experiments in a low-resolution coupled climate model. When Antarctica was assumed to be flat, the north-south asymmetry of the zonal mean top of the atmosphere radiation budget was notably reduced. Doubling CO2 in a flat Antarctica (flat AA) model setup led to a stronger increase in southern hemispheric poleward atmospheric and oceanic heat transport compared to the base model setup. Based on partial radiative perturbation (PRP) computations, it was shown that local radiative feedbacks and an increase in the CO2 forcing in the deeper atmospheric column also contributed to stronger Antarctic warming in the flat AA model setup, and the roles of the individual radiative feedbacks are discussed in some detail. A considerable fraction (between 24 and 80 % for three consecutive 25-year time slices starting in year 51 and ending in year 126 after CO2 doubling) of the polar amplification asymmetry was explained by the difference in surface height, but the fraction was subject to transient changes and might to some extent also depend on model uncertainties. In order to arrive at a more reliable estimate of the role of land height for the observed polar amplification asymmetry, additional studies based on ensemble runs from higher-resolution models and an improved model setup with a more realistic gradual increase in the CO2 concentration are required.

Is our Future Written in the Geological Record of Oceanic Anoxic Events? The Calcareous Nannoplankton Perspective (Invited)

NASA Astrophysics Data System (ADS)

Erba, E.

2013-12-01

The topical emergence of climate change as a crucial issue for society and governments has urged the understanding of the future state of the planet within the context of increasing carbon dioxide concentrations. In the near future, the ocean's uptake of CO2 is expected to rapidly decline because of surface warming, increased vertical stratification, and slowed thermohaline circulation. The Anthropocene CO2 emissions are inferred to be the cause of global warming and alteration of ocean chemistry, triggering unknown responses of marine biota in terms of extinction, innovation and/or temporary adaptations. During the Mesozoic under excess CO2 and greenhouse conditions, the ocean became depleted of oxygen, promoting the burial of massive amounts of organic matter. These episodes are named Oceanic Anoxic Events (OAEs) and might provide guidance as to the response of marine biota to massive CO2 releases and how and at what rate pre-perturbation conditions are eventually restored. After over three decades of research on OAEs, an impressive amount of data has been generated: there is a general consensus on the role of Large Igneous Provinces (LIPs) inducing CO2 increases, greenhouse climate and profound variations in chemical, physical and trophic characteristics of the ocean. OAEs can be studied to decipher the complexity of drivers and of responses within and among different organisms to CO2 pulses, extreme warmth, weathering changes, ocean fertilization and acidification to add the long-term and large-scale prospective to investigations on current, very-short-term and local responses. In Jurassic and Cretaceous oceans, coccolithophores were already a most efficient carbonate-forming group and OAEs offer the opportunity of characterizing variations in their abundance, diversity, and morphology to trace ecological affinities and adaptations to oceanic ecosystem perturbations. We quantitatively investigated the Toarcian OAE, the early Aptian OAE1a and the latest Cenomanian OAE2 and detected major changes in nannofossil abundance, composition and biomineralization, separating most-, intermediate-, and least-tolerant taxa. The T-OAE, OAE1a and OAE2 share similarities in nannoplankton changes, although some differential response was detected. Nannofossil indices highlight strong variability in climate and fertility during OAEs and point to ocean acidification as central distress to calcifying plankton. In general, calcareous phytoplankton show a major calcification failure of heavily calcified forms, ephemeral coccolith dwarfism and malformation possibly representing most remarkable species-specific adjustments to survive surface water acidity. However, different patterns and degree of calcification reduction, dwarfism and malformation during OAEs suggest unequal volcanic CO2 rates, pulses and amount. The duration of OAEs seems a direct measure of LIP-derived excess CO2, hampering biocalcification while turning the oceans into an immense anoxic pool. Changes in ocean chemistry, structure, and fertility during LIP formation might explain observed tempo and mode of nannoplankton evolution: major origination episodes might result from magmas especially enriched in biogeochemically important elements from the mantle.

Linking seafloor volcanism to rising carbon dioxide after the last ice age: observations from the Gulf of California

NASA Astrophysics Data System (ADS)

Rafter, P. A.; Herguera, J. C.; Carriquiry, J. D.; Solomon, E. A.; Southon, J. R.

2017-12-01

Seafloor volcanism at ocean spreading centers may have played an important role in late Pleistocene glacial terminations by increasing the global inventory of the greenhouse gas carbon dioxide (CO2). Gulf of California geology and hydrography offer a unique opportunity to quantify this carbon contribution because CO2 from local seafloor volcanism will reduce/reverse the vertical gradient of seawater radiocarbon (14C). We reconstructed this surface-to-deep gradient by measuring the 14C content of seafloor- and surface-dwelling foraminifera and find several surface-deep 14C reversals during the most recent deglaciation—a 14C distribution that has no analog in the modern ocean. We interpret these observations as representing increased CO2 efflux from the seafloor during deglaciation, linking plate tectonics with the carbon cycle and global climate via enhanced seafloor volcanism.

Climate sensitivity and meridional overturning circulation in the late Eocene using GFDL CM2.1

NASA Astrophysics Data System (ADS)

Hutchinson, David K.; de Boer, Agatha M.; Coxall, Helen K.; Caballero, Rodrigo; Nilsson, Johan; Baatsen, Michiel

2018-06-01

The Eocene-Oligocene transition (EOT), which took place approximately 34 Ma ago, is an interval of great interest in Earth's climate history, due to the inception of the Antarctic ice sheet and major global cooling. Climate simulations of the transition are needed to help interpret proxy data, test mechanistic hypotheses for the transition and determine the climate sensitivity at the time. However, model studies of the EOT thus far typically employ control states designed for a different time period, or ocean resolution on the order of 3°. Here we developed a new higher resolution palaeoclimate model configuration based on the GFDL CM2.1 climate model adapted to a late Eocene (38 Ma) palaeogeography reconstruction. The ocean and atmosphere horizontal resolutions are 1° × 1.5° and 3° × 3.75° respectively. This represents a significant step forward in resolving the ocean geography, gateways and circulation in a coupled climate model of this period. We run the model under three different levels of atmospheric CO2: 400, 800 and 1600 ppm. The model exhibits relatively high sensitivity to CO2 compared with other recent model studies, and thus can capture the expected Eocene high latitude warmth within observed estimates of atmospheric CO2. However, the model does not capture the low meridional temperature gradient seen in proxies. Equatorial sea surface temperatures are too high in the model (30-37 °C) compared with observations (max 32 °C), although observations are lacking in the warmest regions of the western Pacific. The model exhibits bipolar sinking in the North Pacific and Southern Ocean, which persists under all levels of CO2. North Atlantic surface salinities are too fresh to permit sinking (25-30 psu), due to surface transport from the very fresh Arctic ( ˜ 20 psu), where surface salinities approximately agree with Eocene proxy estimates. North Atlantic salinity increases by 1-2 psu when CO2 is halved, and similarly freshens when CO2 is doubled, due to changes in the hydrological cycle.

UV sensitivity of planktonic net community production in ocean surface waters

NASA Astrophysics Data System (ADS)

Regaudie-de-Gioux, Aurore; Agustí, Susana; Duarte, Carlos M.

2014-05-01

The net plankton community metabolism of oceanic surface waters is particularly important as it more directly affects the partial pressure of CO2 in surface waters and thus the air-sea fluxes of CO2. Plankton communities in surface waters are exposed to high irradiance that includes significant ultraviolet blue (UVB, 280-315 nm) radiation. UVB radiation affects both photosynthetic and respiration rates, increase plankton mortality rates, and other metabolic and chemical processes. Here we test the sensitivity of net community production (NCP) to UVB of planktonic communities in surface waters across contrasting regions of the ocean. We observed here that UVB radiation affects net plankton community production at the ocean surface, imposing a shift in NCP by, on average, 50% relative to the values measured when excluding partly UVB. Our results show that under full solar radiation, the metabolic balance shows the prevalence of net heterotrophic community production. The demonstration of an important effect of UVB radiation on NCP in surface waters presented here is of particular relevance in relation to the increased UVB radiation derived from the erosion of the stratospheric ozone layer. Our results encourage design future research to further our understanding of UVB effects on the metabolic balance of plankton communities.

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

NASA Astrophysics Data System (ADS)

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

2013-03-01

Ongoing global warming induced by anthropogenic emissions has opened the debate as to whether geoengineering is a ‘quick fix’ option. Here we analyse the intended and unintended effects of one specific geoengineering approach, which is enhanced weathering via the open ocean dissolution of the silicate-containing mineral olivine. This approach would not only reduce atmospheric CO2 and oppose surface ocean acidification, but would also impact on marine biology. If dissolved in the surface ocean, olivine sequesters 0.28 g carbon per g of olivine dissolved, similar to land-based enhanced weathering. Silicic acid input, a byproduct of the olivine dissolution, alters marine biology because silicate is in certain areas the limiting nutrient for diatoms. As a consequence, our model predicts a shift in phytoplankton species composition towards diatoms, altering the biological carbon pumps. Enhanced olivine dissolution, both on land and in the ocean, therefore needs to be considered as ocean fertilization. From dissolution kinetics we calculate that only olivine particles with a grain size of the order of 1 μm sink slowly enough to enable a nearly complete dissolution. The energy consumption for grinding to this small size might reduce the carbon sequestration efficiency by ˜30%.

Irreversible ocean thermal expansion under carbon dioxide removal

NASA Astrophysics Data System (ADS)

Ehlert, Dana; Zickfeld, Kirsten

2018-03-01

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

Impact of Northern Hemisphere polar gateways on the Arctic Ocean climate during the latest Cretaceous as simulated by an Earth System Model.

NASA Astrophysics Data System (ADS)

Niezgodzki, Igor; Knorr, Gregor; Lohmann, Gerrit; Tyszka, Jarosław

2017-04-01

Using the Earth System Model COSMOS, we simulate the Late Cretaceous climate with different gateway configurations in the Arctic Ocean region under constant CO2 level of 1120 ppm (4 x pre-industrial). Based on the Maastrichtian paleogeography, we modify gateway configurations in the Arctic region according to different scenarios recorded from the Campanian - Maastrichtian ( 83-66 Ma). Our simulation with the Greenland-Norwegian Sea even as deep as 1.5 km in the Campanian produces consistent salinities in the Greenland-Norwegian Sea and in the surface Arctic Ocean, with the proxy-based salinity reconstructions. Towards the end of the Maastrichtian the gateway became shallower but didn't close entirely before the K-Pg boundary. During entire interval, the simulated salinity in the Arctic Ocean was well stratified, in agreement with the data. The surface ocean became progressively fresher, starting from the moderately brackish conditions in the Campanian to the (almost) freshwater conditions around the K-Pg boundary. Arctic gateways configuration changes cannot reproduce cooling trends as reconstructed by the proxy data during the Campanian - Maastrichtian interval. Our additional sensitivity tests with the different CO2 levels (1-6 x pre-industrial) and fixed (Maastrichtian) paleogeography show that a doubling of atmospheric CO2 concentration from 560 ppm to 1120 ppm results in an increase in the zonal mean surface air temperature in the polar regions by as high as 10°C. This suggests that the CO2 level decline, rather than gateway configuration changes, was responsible for the cooling trend toward the end of the Maastrichtian. The research was supported from the grant of the National Science Center in Poland based on the decision DEC-2012/07/N/ST10/03419.

Changing noise levels in a high CO2/lower pH ocean

NASA Astrophysics Data System (ADS)

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

2008-12-01

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

The reef-building coral Siderastrea siderea exhibits parabolic responses to ocean acidification and warming.

PubMed

Castillo, Karl D; Ries, Justin B; Bruno, John F; Westfield, Isaac T

2014-12-22

Anthropogenic increases in atmospheric CO2 over this century are predicted to cause global average surface ocean pH to decline by 0.1-0.3 pH units and sea surface temperature to increase by 1-4°C. We conducted controlled laboratory experiments to investigate the impacts of CO2-induced ocean acidification (pCO2 = 324, 477, 604, 2553 µatm) and warming (25, 28, 32°C) on the calcification rate of the zooxanthellate scleractinian coral Siderastrea siderea, a widespread, abundant and keystone reef-builder in the Caribbean Sea. We show that both acidification and warming cause a parabolic response in the calcification rate within this coral species. Moderate increases in pCO2 and warming, relative to near-present-day values, enhanced coral calcification, with calcification rates declining under the highest pCO2 and thermal conditions. Equivalent responses to acidification and warming were exhibited by colonies across reef zones and the parabolic nature of the corals' response to these stressors was evident across all three of the experiment's 30-day observational intervals. Furthermore, the warming projected by the Intergovernmental Panel on Climate Change for the end of the twenty-first century caused a fivefold decrease in the rate of coral calcification, while the acidification projected for the same interval had no statistically significant impact on the calcification rate-suggesting that ocean warming poses a more immediate threat than acidification for this important coral species.

The reef-building coral Siderastrea siderea exhibits parabolic responses to ocean acidification and warming

PubMed Central

Castillo, Karl D.; Ries, Justin B.; Bruno, John F.; Westfield, Isaac T.

2014-01-01

Anthropogenic increases in atmospheric CO2 over this century are predicted to cause global average surface ocean pH to decline by 0.1–0.3 pH units and sea surface temperature to increase by 1–4°C. We conducted controlled laboratory experiments to investigate the impacts of CO2-induced ocean acidification (pCO2 = 324, 477, 604, 2553 µatm) and warming (25, 28, 32°C) on the calcification rate of the zooxanthellate scleractinian coral Siderastrea siderea, a widespread, abundant and keystone reef-builder in the Caribbean Sea. We show that both acidification and warming cause a parabolic response in the calcification rate within this coral species. Moderate increases in pCO2 and warming, relative to near-present-day values, enhanced coral calcification, with calcification rates declining under the highest pCO2 and thermal conditions. Equivalent responses to acidification and warming were exhibited by colonies across reef zones and the parabolic nature of the corals' response to these stressors was evident across all three of the experiment's 30-day observational intervals. Furthermore, the warming projected by the Intergovernmental Panel on Climate Change for the end of the twenty-first century caused a fivefold decrease in the rate of coral calcification, while the acidification projected for the same interval had no statistically significant impact on the calcification rate—suggesting that ocean warming poses a more immediate threat than acidification for this important coral species. PMID:25377455

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

NASA Astrophysics Data System (ADS)

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

2007-10-01

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

Late Miocene decoupling of oceanic warmth and atmospheric carbon dioxide forcing.

PubMed

LaRiviere, Jonathan P; Ravelo, A Christina; Crimmins, Allison; Dekens, Petra S; Ford, Heather L; Lyle, Mitch; Wara, Michael W

2012-06-06

Deep-time palaeoclimate studies are vitally important for developing a complete understanding of climate responses to changes in the atmospheric carbon dioxide concentration (that is, the atmospheric partial pressure of CO(2), p(co(2))). Although past studies have explored these responses during portions of the Cenozoic era (the most recent 65.5 million years (Myr) of Earth history), comparatively little is known about the climate of the late Miocene (∼12-5 Myr ago), an interval with p(co(2)) values of only 200-350 parts per million by volume but nearly ice-free conditions in the Northern Hemisphere and warmer-than-modern temperatures on the continents. Here we present quantitative geochemical sea surface temperature estimates from the Miocene mid-latitude North Pacific Ocean, and show that oceanic warmth persisted throughout the interval of low p(co(2)) ∼12-5 Myr ago. We also present new stable isotope measurements from the western equatorial Pacific that, in conjunction with previously published data, reveal a long-term trend of thermocline shoaling in the equatorial Pacific since ∼13 Myr ago. We propose that a relatively deep global thermocline, reductions in low-latitude gradients in sea surface temperature, and cloud and water vapour feedbacks may help to explain the warmth of the late Miocene. Additional shoaling of the thermocline after 5 Myr ago probably explains the stronger coupling between p(co(2)), sea surface temperatures and climate that is characteristic of the more recent Pliocene and Pleistocene epochs.

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

NASA Astrophysics Data System (ADS)

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

2008-03-01

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

Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation.

PubMed

Bauska, Thomas K; Baggenstos, Daniel; Brook, Edward J; Mix, Alan C; Marcott, Shaun A; Petrenko, Vasilii V; Schaefer, Hinrich; Severinghaus, Jeffrey P; Lee, James E

2016-03-29

An understanding of the mechanisms that control CO2 change during glacial-interglacial cycles remains elusive. Here we help to constrain changing sources with a high-precision, high-resolution deglacial record of the stable isotopic composition of carbon in CO2(δ(13)C-CO2) in air extracted from ice samples from Taylor Glacier, Antarctica. During the initial rise in atmospheric CO2 from 17.6 to 15.5 ka, these data demarcate a decrease in δ(13)C-CO2, likely due to a weakened oceanic biological pump. From 15.5 to 11.5 ka, the continued atmospheric CO2 rise of 40 ppm is associated with small changes in δ(13)C-CO2, consistent with a nearly equal contribution from a further weakening of the biological pump and rising ocean temperature. These two trends, related to marine sources, are punctuated at 16.3 and 12.9 ka with abrupt, century-scale perturbations in δ(13)C-CO2 that suggest rapid oxidation of organic land carbon or enhanced air-sea gas exchange in the Southern Ocean. Additional century-scale increases in atmospheric CO2 coincident with increases in atmospheric CH4 and Northern Hemisphere temperature at the onset of the Bølling (14.6-14.3 ka) and Holocene (11.6-11.4 ka) intervals are associated with small changes in δ(13)C-CO2, suggesting a combination of sources that included rising surface ocean temperature.

Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation

PubMed Central

Bauska, Thomas K.; Baggenstos, Daniel; Brook, Edward J.; Mix, Alan C.; Marcott, Shaun A.; Petrenko, Vasilii V.; Schaefer, Hinrich; Lee, James E.

2016-01-01

An understanding of the mechanisms that control CO2 change during glacial–interglacial cycles remains elusive. Here we help to constrain changing sources with a high-precision, high-resolution deglacial record of the stable isotopic composition of carbon in CO2 (δ13C-CO2) in air extracted from ice samples from Taylor Glacier, Antarctica. During the initial rise in atmospheric CO2 from 17.6 to 15.5 ka, these data demarcate a decrease in δ13C-CO2, likely due to a weakened oceanic biological pump. From 15.5 to 11.5 ka, the continued atmospheric CO2 rise of 40 ppm is associated with small changes in δ13C-CO2, consistent with a nearly equal contribution from a further weakening of the biological pump and rising ocean temperature. These two trends, related to marine sources, are punctuated at 16.3 and 12.9 ka with abrupt, century-scale perturbations in δ13C-CO2 that suggest rapid oxidation of organic land carbon or enhanced air–sea gas exchange in the Southern Ocean. Additional century-scale increases in atmospheric CO2 coincident with increases in atmospheric CH4 and Northern Hemisphere temperature at the onset of the Bølling (14.6–14.3 ka) and Holocene (11.6–11.4 ka) intervals are associated with small changes in δ13C-CO2, suggesting a combination of sources that included rising surface ocean temperature. PMID:26976561

The abiotically driven biological pump in the ocean and short-term fluctuations in atmospheric CO 2 contents

NASA Astrophysics Data System (ADS)

Ittekkot, Venugopalan

1993-07-01

Current debates on the significance of the oceanic "biological pump" in the removal of atmospheric CO 2 pay more attention to the act of biological carbon-dioxide fixation (primary productivity) in the sea, but pay less or no attention to the equally relevant aspect of the transfer of the fixed carbon to a sink before its oxidation back to CO 2. The upper ocean obviously disqualifies as a sink for biologically fixed CO 2 because of gas-exchange with the atmosphere. The deep ocean, on the other hand, can be a sink at least at time scales of the ocean turnover. Transfer of newly-fixed CO 2 to the deep sea can be accelerated by abiogenic matter introduced to the sea surface from terrestrial sources. This matter acts as ballast and increases the density and settling rates of aggregates of freshly synthesized organic matter thereby facilitating their rapid removal from the upper ocean. Higher supply of abiogenic matter enhances the sequestering of fresh organic matter and in effect shifts the zone of organic matter remineralization from the upper ocean to the deep sea. Consistent with this abiogenic forcing, the rate of organic matter remineralization and the subsequent storage of the remineralized carbon in the deep sea are linked to bulk fluxes (mass accumulation rates) in the deep sea. This mechanism acts as an "abiotic boost" in the workings of the oceanic "biological pump" and results in an increase in deep sea carbon storage; the magnitude of carbon thus stored could have caused the observed short term fluctuations in atmospheric CO 2-contents during the glacial-interglacial cycles.

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

PubMed

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

2017-07-01

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

Reducing Energy-Related CO2 Emissions Using Accelerated Limestone Weathering

DOE Office of Scientific and Technical Information (OSTI.GOV)

Rau, G H; Knauss, K G; Langer, W H

2004-04-27

Following earlier descriptions, the use and impacts of accelerated weathering of limestone AWL; reaction: CO{sub 2} + H{sub 2}O + CaCO{sub 3} {yields} Ca{sup 2+} + 2(HCO{sub 3}{sup -}) as a CO{sub 2} capture and sequestration method is further explored. Since ready access to the ocean is likely an essential requirement for AWL, it is shown that significant limestone resources are relatively close to a majority of CO{sub 2}-emitting power plants along the coastal US. Furthermore, waste fines, representing more than 20% of current US crushed limestone production (>10{sup 9} tonnes/yr), could be used in many instances as an inexpensivemore » or free source of AWL carbonate. With limestone transportation to coastal sites then as the dominant cost variable, CO{sub 2} sequestration (plus capture) costs of $3-$4/tonne are achievable in certain locations. While there is vastly more limestone and water on earth than that required for AWL to capture and sequester all fossil fuel CO{sub 2} production, the transportation cost of bringing limestone, seawater, and waste CO{sub 2} into contact likely limits the method's applicability to perhaps 10-20% of US point-source emissions. Using a bench-scale laboratory reactor, it is shown that CO{sub 2} sequestration rates of 10{sup -6} to 10{sup -5} moles/sec per m{sup 2} of limestone surface area are readily achievable using seawater. This translates into reaction densities as high as 2 x 10{sup -2} tonnes CO{sub 2} m{sup -3}day{sup -1}, highly dependent on limestone particle size, solution turbulence and flow, and CO{sub 2} concentration. Modeling of AWL end-solution disposal in the ocean shows significantly reduced effects on ocean pH and carbonate chemistry relative to those caused by direct CO{sub 2} disposal into the atmosphere or ocean. In fact the increase in ocean Ca{sup 2+} and bicarbonate offered by AWL should significantly enhance the growth of corals and other marine calcifiers whose health is currently being threatened by anthropogenic CO{sub 2} invasion and pH reduction in the ocean.« less

Changes in atmospheric CO2 - Influence of the marine biota at high latitude

NASA Technical Reports Server (NTRS)

Knox, F.; Mcelroy, M. B.

1984-01-01

Approximately half of the nitrogen and phosphorus entering deep waters of the contemporary ocean are transported from the surface in inorganic form as preformed nutrients. A simple model for ocean chemistry is presented and shown to account for the present level of atmospheric CO2. Fluctuations in preformed nutrients, modulated by changes in insolation and circulation at high latitudes, can result in significant variations in CO2. It is suggested that these changes may account for the apparent control on climate exercised by secular variations in the orbital parameters of the earth.

An alternative model for CaCO3 over-shooting during the PETM: Biological carbonate compensation

NASA Astrophysics Data System (ADS)

Luo, Yiming; Boudreau, Bernard P.; Dickens, Gerald R.; Sluijs, Appy; Middelburg, Jack J.

2016-11-01

Decreased CaCO3 content of deep-sea sediments argues for rapid and massive acidification of the oceans during the Paleocene-Eocene Thermal Maximum (PETM, ∼56 Ma BP). In the course of the subsequent recovery from this acidification, sediment CaCO3 content came to exceed pre-PETM levels, known as over-shooting. Past studies have largely attributed the latter to increased alkalinity input to the oceans via enhanced weathering, but this ignores potentially important biological factors. We successfully reproduce the CaCO3 records from Walvis Ridge in the Atlantic Ocean, including over-shooting, using a biogeochemical box model. Replication of the CaCO3 records required: 1) introduction of a maximum of ∼6500 GtC of CO2 directly into deep-ocean waters or ∼8000 GtC into the atmosphere, 2) limited deep-water exchange between the Indo-Atlantic and Pacific oceans, 3) the disappearance of sediment bioturbation during a portion of the PETM, and 4) most central to this study, a ∼50% reduction in net CaCO3 production, during acidification. In our simulations, over-shooting is an emergent property, generated at constant alkalinity input (no weathering feedback) as a consequence of attenuated CaCO3 productivity. This occurs because lower net CaCO3 production from surface waters allows alkalinity to build-up in the deep oceans (alkalinization), thus promoting deep-water super-saturation. Restoration of CaCO3 productivity later in the PETM, particularly in the Indo-Atlantic Ocean, leads to greater accumulation of CaCO3, ergo over-shooting, which returns the ocean to pre-PETM conditions over a time scale greater than 200 ka.

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

NASA Astrophysics Data System (ADS)

Kohfeld, Karen E.; Chase, Zanna

2017-08-01

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

Climate and CO2 coupling in the early Cenozoic Greenhouse

NASA Astrophysics Data System (ADS)

Rae, J. W. B.; Greenop, R.; Kaminski, M.; Sexton, P. F.; Foster, G. L.; Greene, S. E.; Littley, E.; Kirtland Turner, S.; Ridgwell, A.

2017-12-01

The early Cenozoic is a time of climatic extremes: hyperthermals pepper the transition from extreme global warmth to the start of Cenozoic cooling, with these evolving climate regimes accompanied by major changes in ocean chemistry and biota. The exogenic carbon cycle, and ocean-atmospheric CO2 in particular, is thought to have played a key role in these climatic changes, but the carbon chemistry of the early Cenozoic ocean remains poorly constrained. Here we present new boron isotope data from benthic foraminifera, which can be used to constrain relative changes in ocean pH. These are coupled with modelling experiments performed with the cGenie Earth system model to provide new constraints on the carbon cycle and carbonate system of the early Cenozoic. While our benthic boron isotope data do not readily provide a record of surface ocean CO2 , they do place constraints on the whole ocean-atmosphere carbonate system, alongside changes in ocean circulation and biogeochemistry, and also have relatively robust calcite tests and small `vital effects'. During the late Paleocene ascent to peak greenhouse conditions and the middle Eocene descent towards the icehouse, our boron isotope data show close coupling with benthic δ18O, demonstrating a clear link between CO2 and climate. However within the early Eocene our boron isotope data reveal more dynamic changes in deep ocean pH, which may be linked to changes in ocean circulation. Overall, our data demonstrate the ability of CO2 to regulate the climate system across varying boundary conditions, and the influence of both the long-term carbon cycle and shorter-term ocean biogeochemical cycling on Earth's climate.

Efficiency of small scale carbon mitigation by patch iron fertilization

NASA Astrophysics Data System (ADS)

Sarmiento, J. L.; Slater, R. D.; Dunne, J.; Gnanadesikan, A.; Hiscock, M. R.

2010-11-01

While nutrient depletion scenarios have long shown that the high-latitude High Nutrient Low Chlorophyll (HNLC) regions are the most effective for sequestering atmospheric carbon dioxide, recent simulations with prognostic biogeochemical models have suggested that only a fraction of the potential drawdown can be realized. We use a global ocean biogeochemical general circulation model developed at GFDL and Princeton to examine this and related issues. We fertilize two patches in the North and Equatorial Pacific, and two additional patches in the Southern Ocean HNLC region north of the biogeochemical divide and in the Ross Sea south of the biogeochemical divide. We evaluate the simulations using observations from both artificial and natural iron fertilization experiments at nearby locations. We obtain by far the greatest response to iron fertilization at the Ross Sea site, where sea ice prevents escape of sequestered CO2 during the wintertime, and the CO2 removed from the surface ocean by the biological pump is carried into the deep ocean by the circulation. As a consequence, CO2 remains sequestered on century time-scales and the efficiency of fertilization remains almost constant no matter how frequently iron is applied as long as it is confined to the growing season. The second most efficient site is in the Southern Ocean. The North Pacific site has lower initial nutrients and thus a lower efficiency. Fertilization of the Equatorial Pacific leads to an expansion of the suboxic zone and a striking increase in denitrification that causes a sharp reduction in overall surface biological export production and CO2 uptake. The impacts on the oxygen distribution and surface biological export are less prominent at other sites, but nevertheless still a source of concern. The century time scale retention of iron in this model greatly increases the long-term biological response to iron addition as compared with simulations in which the added iron is rapidly scavenged from the ocean.

Antarctic Phytoplankton down-regulate Their Carbon-Concentrating Mechanisms under High CO2 with no Change in Growth Rates

NASA Astrophysics Data System (ADS)

Kranz, S. A.; Young, J. N.; Goldman, J.; Tortell, P. D.; Morel, F. M.

2016-02-01

High-latitude oceans, in particular the coastal Western Antarctic Peninsula (WAP) region of the Southern Ocean, are experiencing a rapidly changing environment due to rising surface ocean temperatures and CO2 concentrations. However, the direct effect of increasing CO2 on polar ocean primary production is unclear, with a number of experiments showing conflicting results. It has been hypothesized that increased CO2 may cause a reduction of the energy-intensive carbon concentrating mechanism (CCM) in phytoplankton, and these energy savings may lead to increased productivity. To test this hypothesis, we incubated natural phytoplankton communities in the WAP under high (800 ppm), current (400 ppm) and low (100 ppm) CO2 for 2 to 3 wk during the austral spring-summer of 2012/2013. In 2 incubations with diatom-dominated phytoplankton assemblages, high CO2 led to a clear down-regulation of CCM activity, as evidenced by an increase in half-saturation constants for CO2, a decrease in external carbonic anhydrase activity and a higher biological fractionation of stable carbon isotopes. In a third incubation, there was no observable regulation of the CCM. We did not observe a significant effect of CO2 on growth rates or community composition in the diatom-dominated communities. The lack of a measureable effect on growth despite CCM down-regulation is likely explained by a very small energetic requirement to concentrate CO2 and saturate Rubisco at low temperatures.

The Hadean-Archaean Environment

PubMed Central

Sleep, Norman H.

2010-01-01

A sparse geological record combined with physics and molecular phylogeny constrains the environmental conditions on the early Earth. The Earth began hot after the moon-forming impact and cooled to the point where liquid water was present in ∼10 million years Subsequently, a few asteroid impacts may have briefly heated surface environments, leaving only thermophile survivors in kilometer-deep rocks. A warm 500 K, 100 bar CO2 greenhouse persisted until subducted oceanic crust sequestered CO2 into the mantle. It is not known whether the Earth's surface lingered in a ∼70°C thermophile environment well into the Archaean or cooled to clement or freezing conditions in the Hadean. Recently discovered ∼4.3 Ga rocks near Hudson Bay may have formed during the warm greenhouse. Alkalic rocks in India indicate carbonate subduction by 4.26 Ga. The presence of 3.8 Ga black shales in Greenland indicates that S-based photosynthesis had evolved in the oceans and likely Fe-based photosynthesis and efficient chemical weathering on land. Overall, mantle derived rocks, especially kimberlites and similar CO2-rich magmas, preserve evidence of subducted upper oceanic crust, ancient surface environments, and biosignatures of photosynthesis. PMID:20516134

Control of air-sea CO2 disequilibria in the subtropical NE Atlantic by planktonic metabolism under the ocean skin

NASA Astrophysics Data System (ADS)

Calleja, María Ll.; Duarte, Carlos M.; Navarro, Nuria; Agustí, Susana

2005-04-01

The air-sea CO2 gradient at the subtropical NE Atlantic was strongly dependent on the metabolism of the planktonic community within the top cms, but independent of that of the communities deeper in the water column. Gross primary production (GPP) and community respiration (R) of the planktonic community within the top cms exceeded those of the communities deeper in the water column by >10-fold and >7 fold, respectively. Net autotrophic metabolism (GPP > R) at the top cms of the water column in some stations drove CO2 uptake by creating a CO2 deficit at the ocean surface, while net heterotrophic metabolism (GPP < R) at the top cms of the water column in other stations resulted in strong CO2 supersaturation, driving CO2 emissions. These results suggest a strong control of the air-sea pCO2 anomaly by intense biological processes.

Exploring the influence of surface waves in the carbon dioxide transfer velocity between the ocean and atmosphere in the coastal region

NASA Astrophysics Data System (ADS)

Ocampo-Torres, Francisco Javier; Francisco Herrera, Carlos; Gutiérrez-Loza, Lucía; Osuna, Pedro

2016-04-01

Field measurements have been carried out in order to better understand the possible influence of ocean surface waves in the transfer of carbon dioxide between the ocean and atmosphere in the coastal zone. The CO2 fluxes are being analysed and results are shown in a contribution by Gutiérrez-Loza et al., in this session. Here we try to highlight the findings regarding the transfer velocity (kCO2) once we have incorporated direct measurements of carbon dioxide concentration in the water side. In this study direct measurements of CO2 fluxes were obtained with an eddy covariance tower located in the shoreline equipped with an infrared open-path gas analyzer (LI-7500, LI-COR) and a sonic anemometer (R3-100 Professional Anemometer, Gill Instruments), both at about 13 m above the mean sea level, and sampling at 20 Hz. For some period of time simultaneous information of waves was recorded with a sampling rate of 2 Hz using an Acoustic Doppler Current Profiler (Workhorse Sentinel, Teledyne RD Instruments) at 10 m depth and 350 m away from the tower. Besides, recently the concentration of CO2 in water has also been recorded making use of a SAMI-CO2 instrument. A subtle effect of the wave field is detected in the estimated kCO2. Looking into details of the surface currents being detected very near the air-sea interface through an ADPC, a certain association can be found with the gas transfer velocity. Furthermore, some of the possible effects of breaking wave induced turbulence in the coastal zone is to be addressed. This work represents a RugDiSMar Project (CONACYT 155793) contribution. The support from CB-2011-01-168173 CONACYT project is greatly acknowledged.

Elevated carbon dioxide alters the plasma composition and behaviour of a shark

PubMed Central

Green, Leon; Jutfelt, Fredrik

2014-01-01

Increased carbon emissions from fossil fuels are increasing the pCO2 of the ocean surface waters in a process called ocean acidification. Elevated water pCO2 can induce physiological and behavioural effects in teleost fishes, although there appear to be large differences in sensitivity between species. There is currently no information available on the possible responses to future ocean acidification in elasmobranch fishes. We exposed small-spotted catsharks (Scyliorhinus canicula) to either control conditions or a year 2100 scenario of 990 μatm pCO2 for four weeks. We did not detect treatment effects on growth, resting metabolic rate, aerobic scope, skin denticle ultrastructure or skin denticle morphology. However, we found that the elevated pCO2 group buffered internal acidosis via accumulation with an associated increase in Na+, indicating that the blood chemistry remained altered despite the long acclimation period. The elevated pCO2 group also exhibited a shift in their nocturnal swimming pattern from a pattern of many starts and stops to more continuous swimming. Although CO2-exposed teleost fishes can display reduced behavioural asymmetry (lateralization), the CO2-exposed sharks showed increased lateralization. These behavioural effects may suggest that elasmobranch neurophysiology is affected by CO2, as in some teleosts, or that the sharks detect CO2 as a constant stressor, which leads to altered behaviour. The potential direct effects of ocean acidification should henceforth be considered when assessing future anthropogenic effects on sharks. PMID:25232027

Parental environment mediates impacts of increased carbon dioxide on a coral reef fish

NASA Astrophysics Data System (ADS)

Miller, Gabrielle M.; Watson, Sue-Ann; Donelson, Jennifer M.; McCormick, Mark I.; Munday, Philip L.

2012-12-01

Carbon dioxide concentrations in the surface ocean are increasing owing to rising CO2 concentrations in the atmosphere. Higher CO2 levels are predicted to affect essential physiological processes of many aquatic organisms, leading to widespread impacts on marine diversity and ecosystem function, especially when combined with the effects of global warming. Yet the ability for marine species to adjust to increasing CO2 levels over many generations is an unresolved issue. Here we show that ocean conditions projected for the end of the century (approximately 1,000μatm CO2 and a temperature rise of 1.5-3.0°C) cause an increase in metabolic rate and decreases in length, weight, condition and survival of juvenile fish. However, these effects are absent or reversed when parents also experience high CO2 concentrations. Our results show that non-genetic parental effects can dramatically alter the response of marine organisms to increasing CO2 and demonstrate that some species have more capacity to acclimate to ocean acidification than previously thought.

Carbonate counter pump stimulated by natural iron fertilization in the Polar Frontal Zone

NASA Astrophysics Data System (ADS)

Salter, Ian; Schiebel, Ralf; Ziveri, Patrizia; Movellan, Aurore; Lampitt, Richard; Wolff, George A.

2014-12-01

The production of organic carbon in the ocean's surface and its subsequent downward export transfers carbon dioxide to the deep ocean. This CO2 drawdown is countered by the biological precipitation of carbonate, followed by sinking of particulate inorganic carbon, which is a source of carbon dioxide to the surface ocean, and hence the atmosphere over 100-1,000 year timescales. The net transfer of CO2 to the deep ocean is therefore dependent on the relative amount of organic and inorganic carbon in sinking particles. In the Southern Ocean, iron fertilization has been shown to increase the export of organic carbon, but it is unclear to what degree this effect is compensated by the export of inorganic carbon. Here we assess the composition of sinking particles collected from sediment traps located in the Polar Frontal Zone of the Southern Ocean. We find that in high-nutrient, low-chlorophyll regions that are characterized by naturally high iron concentrations, fluxes of both organic and inorganic carbon are higher than in regions with no iron fertilization. However, the excess flux of inorganic carbon is greater than that of organic carbon. We estimate that the production and flux of carbonate in naturally iron-fertilized waters reduces the overall amount of CO2 transferred to the deep ocean by 6-32%, compared to 1-4% at the non-fertilized site. We suggest that an increased export of organic carbon, stimulated by iron availability in the glacial sub-Antarctic oceans, may have been accompanied by a strengthened carbonate counter pump.

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

NASA Astrophysics Data System (ADS)

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

2012-03-01

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 (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 an actively 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 gradually disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice flow thickness by ca. 0.2 m per week and resulted in an estimated 1.6 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air-sea CO2 uptake of 11 mmol m-2 sea ice d-1 or to 3.5 ton km-2 ice floe week-1.

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

NASA Astrophysics Data System (ADS)

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.

Theoretical constraints on oxygen and carbon dioxide concentrations in the Precambrian atmosphere

NASA Technical Reports Server (NTRS)

Kasting, J. F.

1987-01-01

Simple (one-dimensional) climate models suggest that carbon dioxide concentrations during the Archean must have been at least 100-1000 times the present level to keep the Earth's surface temperature above freezing in the face of decreased solar luminosity. Such models provide only lower bounds on CO2, so it is possible that CO2 levels were substantially higher than this and that the Archean climate was much warmer than today. Periods of extensive glaciation during the early and late Proterozoic, on the other hand, indicate that the climate at these times was relatively cool. To be consistent with climate models CO2 partial pressures must have declined from approximately 0.03 to 0.3 bar around 2.5 Ga ago to between 10(-3) and 10(-2) bar at 0.8 Ga ago. This steep decrease in carbon dioxide concentrations may be inconsistent with paleosol data, which implies that pCO2 did not change appreciably during that time. Oxygen was essentially absent from the Earth's atmosphere and oceans prior to the emergence of a photosynthetic source, probably during the late Archean. During the early Proterozoic the atmosphere and surface ocean were apparently oxidizing, while the deep ocean remained reducing. An upper limit of 6 x 10(-3) bar for pO2 at this time can be derived by balancing the burial rate of organic carbon with the rate of oxidation of ferrous iron in the deep ocean. The establishment of oxidizing conditions in the deep ocean, marked by the disappearance of banded iron formations approximately 1.7 Ga ago, permitted atmospheric oxygen to climb to its present level. O2 concentrations may have remained substantially lower than today, however, until well into the Phanerozoic.

Strangelove Ocean and Deposition of Unusual Shallow-Water Carbonates After the End-Permian Mass Extinction

NASA Technical Reports Server (NTRS)

Rampino, Michael R.; Caldeira, Ken

2003-01-01

The severe mass extinction of marine and terrestrial organisms at the end of the Permian Period (approx. 251 Ma) was accompanied by a rapid negative excursion of approx. 3 to 4 per mil in the carbon-isotope ratio of the global surface oceans and atmosphere that persisted for some 500,000 into the Early Triassic. Simulations with an ocean-atmosphere/carbon-cycle model suggest that the isotope excursion can be explained by collapse of ocean primary productivity (a Strangelove Ocean) and changes in the delivery and cycling of carbon in the ocean and on land. Model results also suggest that perturbations of the global carbon cycle resulting from the extinctions led to short-term fluctuations in atmospheric pCO2 and ocean carbonate deposition, and to a long-term (>1 Ma) decrease in sedimentary burial of organic carbon in the Triassic. Deposition of calcium carbonate is a major sink of river-derived ocean alkalinity and for CO2 from the ocean/atmosphere system. The end of the Permian was marked by extinction of most calcium carbonate secreting organisms. Therefore, the reduction of carbonate accumulation made the oceans vulnerable to a build-up of alkalinity and related fluctuations in atmospheric CO2. Our model results suggest that an increase in ocean carbonate-ion concentration should cause increased carbonate accumulation rates in shallow-water settings. After the end-Permian extinctions, early Triassic shallow-water sediments show an abundance of abiogenic and microbial carbonates that removed CaCO3 from the ocean and may have prevented a full 'ocean-alkalinity crisis' from developing.

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

NASA Astrophysics Data System (ADS)

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) (< 200 µatm) in the Chukchi Sea of the western Arctic 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 (< 27) and pCO2sea was closer to the air-sea CO2 equilibrium (˜ 360 µatm). From the relationships between salinity and total alkalinity, we confirmed that the low salinity in the Canada Basin was due to the larger fraction of meltwater input (˜ 0.16) rather than the riverine discharge (˜ 0.1). Such an increase in pCO2sea was not so clear in the coastal region near Point Barrow, where the fraction of riverine discharge was larger than that of sea-ice melt. We also identified low pCO2sea (< 250 µatm) in the depth of 30-50 m under the halocline of the Canada Basin. This subsurface low pCO2sea was attributed to the advection of Pacific-origin water, in which dissolved inorganic carbon is relatively low, through the Chukchi Sea where net primary production is high. Oxygen supersaturation (> 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.

Utilizing Ocean Thermal Energy in a Submarine Robot

NASA Technical Reports Server (NTRS)

Jones, Jack; Chao, Yi

2009-01-01

A proposed system would exploit the ocean thermal gradient for recharging the batteries in a battery-powered unmanned underwater vehicle [UUV (essentially, a small exploratory submarine robot)] of a type that has been deployed in large numbers in research pertaining to global warming. A UUV of this type travels between the ocean surface and depths, measuring temperature and salinity. The proposed system is related to, but not the same as, previously reported ocean thermal energy conversion (OTEC) systems that exploit the ocean thermal gradient but consist of stationary apparatuses that span large depth ranges. The system would include a turbine driven by working fluid subjected to a thermodynamic cycle. CO2 has been provisionally chosen as the working fluid because it has the requisite physical properties for use in the range of temperatures expected to be encountered in operation, is not flammable, and is much less toxic than are many other commercially available refrigerant fluids. The system would be housed in a pressurized central compartment in a UUV equipped with a double hull (see figure). The thermodynamic cycle would begin when the UUV was at maximum depth, where some of the CO2 would condense and be stored, at relatively low temperature and pressure, in the annular volume between the inner and outer hulls. The cycle would resume once the UUV had ascended to near the surface, where the ocean temperature is typically greater than or equals 20 C. At this temperature, the CO2 previously stored at depth in the annular volume between the inner and outer hulls would be pressurized to approx. equals 57 bar (5.7 MPa). The pressurized gaseous CO2 would flow through a check valve into a bladder inside the pressurized compartment, thereby storing energy of the relatively warm, pressurized CO2 for subsequent use after the next descent to maximum depth.

Significant discharge of CO2 from hydrothermalism associated with the submarine volcano of El Hierro Island

NASA Astrophysics Data System (ADS)

Santana-Casiano, J. M.; Fraile-Nuez, E.; González-Dávila, M.; Baker, E. T.; Resing, J. A.; Walker, S. L.

2016-05-01

The residual hydrothermalism associated with submarine volcanoes, following an eruption event, plays an important role in the supply of CO2 to the ocean. The emitted CO2 increases the acidity of seawater. The submarine volcano of El Hierro, in its degasification stage, provided an excellent opportunity to study the effect of volcanic CO2 on the seawater carbonate system, the global carbon flux, and local ocean acidification. A detailed survey of the volcanic edifice was carried out using seven CTD-pH-ORP tow-yo studies, localizing the redox and acidic changes, which were used to obtain surface maps of anomalies. In order to investigate the temporal variability of the system, two CTD-pH-ORP yo-yo studies were conducted that included discrete sampling for carbonate system parameters. Meridional tow-yos were used to calculate the amount of volcanic CO2 added to the water column for each surveyed section. The inputs of CO2 along multiple sections combined with measurements of oceanic currents produced an estimated volcanic CO2 flux = 6.0 105 ± 1.1 105 kg d-1 which is ~0.1% of global volcanic CO2 flux. Finally, the CO2 emitted by El Hierro increases the acidity above the volcano by ~20%.

Significant discharge of CO2 from hydrothermalism associated with the submarine volcano of El Hierro Island.

PubMed

Santana-Casiano, J M; Fraile-Nuez, E; González-Dávila, M; Baker, E T; Resing, J A; Walker, S L

2016-05-09

The residual hydrothermalism associated with submarine volcanoes, following an eruption event, plays an important role in the supply of CO2 to the ocean. The emitted CO2 increases the acidity of seawater. The submarine volcano of El Hierro, in its degasification stage, provided an excellent opportunity to study the effect of volcanic CO2 on the seawater carbonate system, the global carbon flux, and local ocean acidification. A detailed survey of the volcanic edifice was carried out using seven CTD-pH-ORP tow-yo studies, localizing the redox and acidic changes, which were used to obtain surface maps of anomalies. In order to investigate the temporal variability of the system, two CTD-pH-ORP yo-yo studies were conducted that included discrete sampling for carbonate system parameters. Meridional tow-yos were used to calculate the amount of volcanic CO2 added to the water column for each surveyed section. The inputs of CO2 along multiple sections combined with measurements of oceanic currents produced an estimated volcanic CO2 flux = 6.0 10(5) ± 1.1 10(5 )kg d(-1) which is ~0.1% of global volcanic CO2 flux. Finally, the CO2 emitted by El Hierro increases the acidity above the volcano by ~20%.

Significant discharge of CO2 from hydrothermalism associated with the submarine volcano of El Hierro Island

PubMed Central

Santana-Casiano, J. M.; Fraile-Nuez, E.; González-Dávila, M.; Baker, E. T.; Resing, J. A.; Walker, S. L.

2016-01-01

The residual hydrothermalism associated with submarine volcanoes, following an eruption event, plays an important role in the supply of CO2 to the ocean. The emitted CO2 increases the acidity of seawater. The submarine volcano of El Hierro, in its degasification stage, provided an excellent opportunity to study the effect of volcanic CO2 on the seawater carbonate system, the global carbon flux, and local ocean acidification. A detailed survey of the volcanic edifice was carried out using seven CTD-pH-ORP tow-yo studies, localizing the redox and acidic changes, which were used to obtain surface maps of anomalies. In order to investigate the temporal variability of the system, two CTD-pH-ORP yo-yo studies were conducted that included discrete sampling for carbonate system parameters. Meridional tow-yos were used to calculate the amount of volcanic CO2 added to the water column for each surveyed section. The inputs of CO2 along multiple sections combined with measurements of oceanic currents produced an estimated volcanic CO2 flux = 6.0 105 ± 1.1 105 kg d−1 which is ~0.1% of global volcanic CO2 flux. Finally, the CO2 emitted by El Hierro increases the acidity above the volcano by ~20%. PMID:27157062

Calcareous Nannoplankton Response to Surface-Water Acidification Around Oceanic Anoxic Event 1a

NASA Astrophysics Data System (ADS)

Erba, Elisabetta; Bottini, Cinzia; Weissert, Helmut J.; Keller, Christina E.

2010-07-01

Ocean acidification induced by atmospheric CO2 may be a major threat to marine ecosystems, particularly to calcareous nannoplankton. We show that, during the Aptian (~120 million years ago) Oceanic Anoxic Event 1a, which resulted from a massive addition of volcanic CO2, the morphological features of calcareous nannofossils traced the biological response to acidified surface waters. We observe the demise of heavily calcified nannoconids and reduced calcite paleofluxes at the beginning of a pre-anoxia calcification crisis. Ephemeral coccolith dwarfism and malformation represent species-specific adjustments to survive lower pH, whereas later, abundance peaks indicate intermittent alkalinity recovery. Deepwater acidification occurred with a delay of 25,000 to 30,000 years. After the dissolution climax, nannoplankton and carbonate recovery developed over ~160,000 years under persisting global dysoxia-anoxia.

Adverse effects of ocean acidification on early development of squid (Doryteuthis pealeii).

PubMed

Kaplan, Maxwell B; Mooney, T Aran; McCorkle, Daniel C; Cohen, Anne L

2013-01-01

Anthropogenic carbon dioxide (CO2) is being absorbed into the ocean, altering seawater chemistry, with potentially negative impacts on a wide range of marine organisms. The early life stages of invertebrates with internal and external aragonite structures may be particularly vulnerable to this ocean acidification. Impacts to cephalopods, which form aragonite cuttlebones and statoliths, are of concern because of the central role they play in many ocean ecosystems and because of their importance to global fisheries. Atlantic longfin squid (Doryteuthis pealeii), an ecologically and economically valuable taxon, were reared from eggs to hatchlings (paralarvae) under ambient and elevated CO2 concentrations in replicated experimental trials. Animals raised under elevated pCO2 demonstrated significant developmental changes including increased time to hatching and shorter mantle lengths, although differences were small. Aragonite statoliths, critical for balance and detecting movement, had significantly reduced surface area and were abnormally shaped with increased porosity and altered crystal structure in elevated pCO2-reared paralarvae. These developmental and physiological effects could alter squid paralarvae behavior and survival in the wild, directly and indirectly impacting marine food webs and commercial fisheries.

Adverse Effects of Ocean Acidification on Early Development of Squid (Doryteuthis pealeii)

PubMed Central

Kaplan, Maxwell B.; Mooney, T. Aran; McCorkle, Daniel C.; Cohen, Anne L.

2013-01-01

Anthropogenic carbon dioxide (CO2) is being absorbed into the ocean, altering seawater chemistry, with potentially negative impacts on a wide range of marine organisms. The early life stages of invertebrates with internal and external aragonite structures may be particularly vulnerable to this ocean acidification. Impacts to cephalopods, which form aragonite cuttlebones and statoliths, are of concern because of the central role they play in many ocean ecosystems and because of their importance to global fisheries. Atlantic longfin squid (Doryteuthis pealeii), an ecologically and economically valuable taxon, were reared from eggs to hatchlings (paralarvae) under ambient and elevated CO2 concentrations in replicated experimental trials. Animals raised under elevated pCO2 demonstrated significant developmental changes including increased time to hatching and shorter mantle lengths, although differences were small. Aragonite statoliths, critical for balance and detecting movement, had significantly reduced surface area and were abnormally shaped with increased porosity and altered crystal structure in elevated pCO2-reared paralarvae. These developmental and physiological effects could alter squid paralarvae behavior and survival in the wild, directly and indirectly impacting marine food webs and commercial fisheries. PMID:23741298

21st Century Carbon-Climate Change as Simulated by the Canadian Earth System Model CanESM1

NASA Astrophysics Data System (ADS)

Curry, C.; Christian, J. R.; Arora, V.; Boer, G. J.; Denman, K. L.; Flato, G. M.; Scinocca, J. F.; Merryfield, W. J.; Lee, W. G.; Yang, D.

2009-12-01

The Canadian Earth System Model CanESM1 is a fully coupled climate/carbon-cycle model with prognostic ocean and terrestrial components. The model has been used to simulate the 1850-2000 climate using historical greenhouse gas emissions, and future climates using IPCC emission scenarios. Modelled globally averaged CO2 concentration, land and ocean carbon uptake compare well with observation-based values at year 2000, as do the annual cycle and latitudinal distribution of CO2, instilling confidence that the model is suitable for future projections of carbon cycle behaviour in a changing climate. Land use change emissions are calculated explicitly using an observation-based time series of fractional coverage of different plant functional types. A more complete description of the model may be found in Arora et al. (2009). Differences in the land-atmosphere CO2 flux from the present to the future period under the SRES A2 emissions scenario show an increase in land sinks by a factor of 7.5 globally, mostly the result of CO2 fertilization. By contrast, the magnitude of the global ocean CO2 sink increases by a factor of only 2.3 by 2100. Expressed as a fraction of total emissions, ocean carbon uptake decreases throughout the 2000-2100 period, while land carbon uptake increases until around 2050, then declines. The result is an increase in airborne CO2 fraction after the mid-21st century, reaching a value of 0.55 by 2100. The simulated decline in ocean carbon uptake over the 21st century occurs despite steadily rising atmospheric CO2. This behaviour is usually attributed to climate-induced changes in surface temperature and salinity that reduce CO2 solubility, and increasing ocean stratification that weakens the biological pump. However, ocean biological processes such as dinitrogen fixation and calcification may also play an important role. Although not well understood at present, improved parameterizations of these processes will increase confidence in projections of future trends in CO2 uptake.

Connecting the Mississippi River with Carbon Variability in the Gulf of Mexico

NASA Astrophysics Data System (ADS)

Xue, Z. G.; He, R.; Fennel, K.; Cai, W. J.; Lohrenz, S. E.; Huang, W. J.; Tian, H.; Ren, W.

2016-02-01

To understand the linkage between landuse/land-cover change within the Mississippi basin and the carbon dynamics in the Gulf of Mexico, a three-dimensional coupled physical-biogeochemical model was used to the examine temporal and spatial variability of surface ocean pCO2 in the Gulf of Mexico (GoM). The model is driven by realistic atmospheric forcing, open boundary conditions from a data-assimilative global ocean circulation model, and freshwater and terrestrial nutrient and carbon input from major rivers provided by the Dynamic Land Ecosystem Model (DLEM). A seven-year model hindcast (2004-2010) was performed and was validated against the recently updated Lamont-Doherty Earth Observatory global ocean carbon dataset. Model simulated seawater pCO2 and air-sea CO2 flux are in good agreement with in-situ measurements. An inorganic carbon budget was estimated based on the multi-year mean of the model results. Overall, the GoM is a sink of atmospheric CO2 with a flux of 0.92 × 1012 mol C yr-1, which, together with the enormous fluvial carbon input, is balanced by carbon export through the Loop Current. In a sensitivity experiment with all biological sources and sinks of carbon disabled surface pCO2 was elevated by 70 ppm, suggesting that biological uptake is the most important reason for the simulated CO2 sink. The impact from landuse and land-cover changes within the Mississippi River basin on coastal pCO2 dynamics is also discussed based on a scenario run driven by river conditions during the 1904-1910 provided by the DLEM model.

Trichodesmium’s strategies to alleviate phosphorus limitation in the future acidified oceans.

PubMed

Spungin, Dina; Berman-Frank, Ilana; Levitan, Orly

2014-06-01

Global warming may exacerbate inorganic nutrient limitation, including phosphorus (P), in the surface waters of tropical oceans that are home to extensive blooms of the marine diazotrophic cyanobacterium, Trichodesmium. We examined the combined effects of P limitation and pCO(2), forecast under ocean acidification scenarios, on Trichodesmium erythraeum IMS101 cultures. We measured nitrogen acquisition,glutamine synthetase activity, C uptake rates, intracellular Adenosine Triphosphate (ATP) concentration and the pool sizes of related key proteins. Here, we present data supporting the idea that cellular energy re-allocation enables the higher growth and N(2) fixation rates detected in Trichodesmium cultured under high pCO(2). This is reflected in altered protein abundance and metabolic pools. Also modified are particulate organic carbon and nitrogen production rates,enzymatic activities, and cellular ATP concentrations. We suggest that adjusting these cellular pathways to changing environmental conditions enables Trichodesmium to compensate for low P availability and to thrive in acidified oceans. Moreover, elevated pCO(2) could provide Trichodesmium with a competitive dominance that would extend its niche, particularly in P-limited regions of the tropical and subtropical oceans.

Evolution of surface and deep water conditions in the Antarctic Southern Ocean across the MPT

NASA Astrophysics Data System (ADS)

Hasenfratz, A. P.; Jaccard, S.; Martinez-Garcia, A.; Hodell, D. A.; Vance, D.; Bernasconi, S. M.; Kleiven, H. F.; Haug, G. H.

2016-12-01

The mid-Pleistocene transition (MPT; 1.25-0.7 Myr) marked a fundamental change in the periodicity of the climate cycles, shifting from a 41-kyr to a high-amplitude, asymmetric 100-kyr cycle without any noticeable change in orbital forcing. Hypotheses to explain the MPT involve non-linear responses to orbital forcing, changes in glacial dynamics and internal changes in the carbon cycle. Specifically, a decrease in pCO2 during peak ice age conditions and the associated global cooling has been proposed as one of the possible triggers for the MPT. Previous results have indicated that the Southern Ocean provides a coherent two-part mechanism for the timing and amplitude of the glacial/interglacial pCO2 variations. However, there is still much uncertainty and debate regarding the response of the Antarctic Southern Ocean biogeochemistry to changes invoked for the MPT, and its contribution to the proposed pCO2 variations. Here, we show 1.5 Myr-long records of export production, and planktonic (Neogloboquadrina pachyderma) and benthic (Melonis pompilioides) foraminiferal stable isotopes and trace metals from ODP Site 1094 retrieved from the Atlantic sector of the Antarctic Southern Ocean (53.2°S, 5.1°E, 2807m). While glacial planktonic δ18O increases across the MPT, glacial Mg/Ca-derived SST decrease later, around 700 ka, when glacial atmospheric pCO2 has already dropped. As glacial export production that is crucially related to micronutrients upwelled from the subsurface ocean remains unchanged across the past 1.5 Myr, it seems that cooling of the glacial surface ocean did not significantly alter the stability of the water column. Furthermore, paired measurements of benthic δ18O and Mg/Ca enables the determination of seawater δ18O of the deep ocean, which allows us to estimate changes in the density gradient and the salinity of the deep water.

The role of North Atlantic Ocean circulation and biological sequestration on atmospheric CO2 uptake during the last deglaciation (CL Division Outstanding ECS Award Lecture)

NASA Astrophysics Data System (ADS)

Muschitiello, Francesco; D'Andrea, William J.; Dokken, Trond M.; Schmittner, Andreas

2017-04-01

Understanding the impact of ocean circulation on the global atmospheric CO2 budget is of paramount importance for anticipating the consequences of projected future changes in Atlantic Meridional Overturning Circulation (AMOC). In particular, the efficiency of the oceanic biological pump can impact atmospheric CO2 through changes in vertical carbon export mediated by variations in the nutrient inventory of the North Atlantic basin. However, the causal relationship between North Atlantic Ocean circulation, biological carbon sequestration, and atmospheric CO2 is poorly understood. Here we present new high-resolution planktic-benthic 14C data and biomarker records from an exceptionally well-dated marine core from the Nordic Seas spanning the last deglaciation ( 15,000-10,000 years BP). The records document for the first time large and rapid atmospheric CO2 drawdowns and increase in plankton stocks during major North Atlantic cooling events. Using transient climate simulations from a fully coupled climate-biosphere model, we show that minor perturbations of the North Atlantic biological pump resulting from surface freshening and AMOC weakening can have a major impact on the global atmospheric CO2 budget. Furthermore, our data help clarifying the timing and magnitude of the deglacial CO2 signal recorded in Antarctic ice cores. We conclude that the global CO2 budget is more sensitive to perturbations in North Atlantic circulation than previously thought, which has significance in the future debate of the AMOC response to anthropogenic warming.

An 'outrageous hypothesis' for Mars - Episodic oceans

NASA Astrophysics Data System (ADS)

Kerr, R. A.

1993-02-01

The conventional view of Mars is that, during the past 3 billion years, the atmosphere has been so thin and cold that the planet's water has remained locked up underground as ice. However, Baker et al. (1991) proposed a radically different and far-reaching alternative: a Mars that is periodically shrouded in an earthlike atmosphere, with a temporary ocean and massive ice sheets. This hypothesis was proposed in order to explain the assortment of surface features sent back by the Viking spacecraft in 1970, such as huge channels, apparent ocean shorelines, and possible glacial landforms. To support this hypothesis, Baker and his coworkers invoked a spate of catastrophic floods, all cutting their channels at the same geological moment due a great outburst of Mars's volcanic activity which could have melted some subsurface ice and belched out CO2. This gas, together with some additional CO2 released as the water interacted with the surface, caused a strong greenhouse warming, causing melting of underground ice and the formation of an ocean.

Seasonally different carbon flux changes in the Southern Ocean in response to the southern annular mode.

PubMed

Hauck, J; Völker, C; Wang, T; Hoppema, M; Losch, M; Wolf-Gladrow, D A

2013-12-01

Stratospheric ozone depletion and emission of greenhouse gases lead to a trend of the southern annular mode (SAM) toward its high-index polarity. The positive phase of the SAM is characterized by stronger than usual westerly winds that induce changes in the physical carbon transport. Changes in the natural carbon budget of the upper 100 m of the Southern Ocean in response to a positive SAM phase are explored with a coupled ecosystem-general circulation model and regression analysis. Previously overlooked processes that are important for the upper ocean carbon budget during a positive SAM period are identified, namely, export production and downward transport of carbon north of the polar front (PF) as large as the upwelling in the south. The limiting micronutrient iron is brought into the surface layer by upwelling and stimulates phytoplankton growth and export production but only in summer. This leads to a drawdown of carbon and less summertime outgassing (or more uptake) of natural CO 2 . In winter, biological mechanisms are inactive, and the surface ocean equilibrates with the atmosphere by releasing CO 2 . In the annual mean, the upper ocean region south of the PF loses more carbon by additional export production than by the release of CO 2 into the atmosphere, highlighting the role of the biological carbon pump in response to a positive SAM event.

Remote sensing algorithm for sea surface CO2 in the Baltic Sea

NASA Astrophysics Data System (ADS)

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.

Mantle Volatiles and Global Carbon Flux and Budget

NASA Astrophysics Data System (ADS)

Zhang, Y.

2014-12-01

The global volcanic carbon flux to the surface of Earth is a fundamental parameter in understanding the global carbon cycle that includes deep carbon as well as the degassing history of the mantle. The flux has been estimated before (e.g., Marty and Tolstikhin, 1998). Recent progress has significantly revised some of the parameters used in the estimation, e.g., the oceanic 3He flux has been re-evaluated (Bianchi et al., 2010) to be only about half of the earlier widely-used estimate, and numerous subaerial volcanic degassing data are now available. In this report, a new attempt is made to assess the global carbon flux and budget. Rather than dividing the carbon flux by categories of MORB, Plumes and Arcs, we estimate the global carbon flux by considering oceanic and subaerial volcanism. The oceanic 3He flux is 527±102 mol/yr (Bianchi et al., 2010). Most of the flux is from spreading ridges with only minor contributions from submarine oceanic hotspots or arc volcanism. Hence, the mean CO2/3He ratio in MORB is applied to estimate oceanic flux of CO2. The subaerial CO2 flux is based on evaluation of different arc segments and is messier to compute. Literature estimates use estimated SO2 flux in the last tens of years combined with estimated CO2/SO2 degassing ratios (Hilton et al., 2002; Fischer, 2008). Assuming that the last tens of years are representative of recent geological times in terms of volcanic degassing, the estimated global CO2 flux still depends critically on a couple of arcs that are main contributors of the subaerial volcanic CO2 flux, and those seem to have been rather loosely constrained before. Using recently available data (although there are still holes), we derive a new global subaerial volcanic CO2 flux. By combining with oceanic volcanic CO2 flux, we obtain at a new global flux. The significance of the new estimate to the global volatile budget will be discussed.

Millennial-scale variability in dust deposition, marine export production, and nutrient consumption in the glacial subantarctic ocean (Invited)

NASA Astrophysics Data System (ADS)

Martinez-Garcia, A.; Sigman, D. M.; Anderson, R. F.; Ren, H. A.; Hodell, D. A.; Straub, M.; Jaccard, S.; Eglinton, T. I.; Haug, G. H.

2013-12-01

Based on the limitation of modern Southern Ocean phytoplankton by iron and the evidence of higher iron-bearing dust fluxes to the ocean during ice ages, it has been proposed that iron fertilization of Southern Ocean phytoplankton contributed to the reduction in atmospheric CO2 during ice ages. In the Subantarctic zone of the Atlantic Southern Ocean, glacial increases in dust flux and export production have been documented, supporting the iron fertilization hypothesis. However, these observations could be interpreted alternatively as resulting from the equatorward migration of Southern Ocean fronts during ice ages if the observed productivity rise was not accompanied by an increase in major nutrient consumption. Here, new 230Th-normalized lithogenic and opal fluxes are combined with high-resolution biomarker measurements to reconstruct millennial-scale changes in dust deposition and marine export production in the subantarctic Atlantic over the last glacial cycle. In the same record foraminifera-bound nitrogen isotopes are used to reconstruct ice age changes in surface nitrate utilization, providing a comprehensive test of the iron fertilization hypothesis. Elevation in foraminifera-bound δ15N, indicating more complete nitrate consumption, coincides with times of surface cooling and greater dust flux and export production. These observations indicate that the ice age Subantarctic was characterized by iron fertilized phytoplankton growth. The resulting strengthening of the Southern Ocean's biological pump can explain the ~40 ppm lowering of CO2 that characterizes the transitions from mid-climate states to full ice age conditions as well as the millennial-scale atmospheric CO2 fluctuations observed within the last ice age

On the radiocarbon record in banded corals: exchange parameters and net transport of /sup 14/CO/sub 2/ between atmosphere and surface ocean

DOE Office of Scientific and Technical Information (OSTI.GOV)

Druffel, E.M.; Suess, H.E.

1983-02-20

We have made radiocarbon measurements of banded hermatypic corals from Florida, Belize, and the Galapagos Islands. Interpretation is presented here of these previously reported results. These measurements represent the /sup 14/C//sup 12/C ratios in dissolved inorganic carbon (DIOC) in the surface ocean waters of the Gulf Stream and the Peru Current at the time of coral ring formation. A depletion in radiocarbon concentration was observed incoral rings that grew from A.D. 1900--1952. It was caused by dilution of existing /sup 14/C levels with dead CO/sub 2/ from fossil fuel burning (the Suess effect, or S/sub e/). A similar trend wasmore » observed in the distribution of bomb-produced /sup 14/C in corals that had grown during the years following A.D. 1952. The concentration of bomb-produced radiocarbon was much higher in corals from temperate regions (Florida, Belize, Hawaiian Islands) than in corals from tropical regions (Galapagos Islands and Canton Island). The apparent radiocarbon ages of the surface waters in temperate and tropical oceans during the preanthropogenic period range from about 280 to 520 years B.P. (-40 to -69%). At all investigated locations, it is likely that waters at subsurface depths have the same apparent radiocarbon age of about 670 years B.P. From the change of oceanic ..delta../sup 14/C in the surface during post-bomb times, the approximate annual rate of net input of /sup 14/CO/sub 2/ to the ocean waters is calculated to be about 8% of the prevailing /sup 14/C difference between atmosphere and ocean. From this input and from preanthropogenic ..delta../sup 14/C values found at each location, it can be seen that vertical mixing of water in the Peru Current is about 3 times greater than that in the Gulf Stream.« less

Quantifying the Observability of CO2 Flux Uncertainty in Atmospheric CO2 Records Using Products from Nasa's Carbon Monitoring Flux Pilot Project

NASA Technical Reports Server (NTRS)

Ott, Lesley; Pawson, Steven; Collatz, Jim; Watson, Gregg; Menemenlis, Dimitris; Brix, Holger; Rousseaux, Cecile; Bowman, Kevin; Bowman, Kevin; Liu, Junjie;

CO2-dominated Atmosphere in Equilibrium with NH3-H2O Ocean: Application to Early Titan and Ocean Planets

NASA Astrophysics Data System (ADS)

Marounina, N.; Grasset, O.; Tobie, G.; Carpy, S.

2015-12-01

During the accretion of Titan, impact heating may have been sufficient to allow the global melting of water ice (Monteux et al. 2014) and the release of volatile compounds, with CO2 and NH3 as main constituents (Tobie et al. 2012). Thus, on primitive Titan, it is thought that a massive atmosphere was in contact with a global water ocean. Similar configurations may occur on temperate water-rich planets called ocean planets (Léger et al. 2004, Kitzmann et al. 2015).Due to its rather low solubility in liquid water, carbon dioxide is expected to be one of the major components in the atmosphere. The atmospheric amount of CO2 is a key parameter for assessing the thermal evolution of the planetary surface because of its strong greenhouse effect. However, ammonia significantly affects the solubility of CO2 in water and hence the atmosphere-ocean thermo-chemical equilibrium. For primitive Titan, estimating the mass, temperature and composition of the primitive atmosphere is important to determine mechanisms that led to the present-day N2-CH4 dominated atmosphere. Similarly, for ocean planets, the influence of ammonia on the atmospheric abundance in CO2 has consequences for the definition of the habitable zone.To investigate the atmospheric composition of the water-rich worlds for a wide range of initial compositions, we have developed a vapor-liquid equilibrium model of the NH3-CO2-H2O system, where we account for the non-ideal comportment of both vapor and liquid phases and the ion speciation of volatiles dissolved in the aqueous phase. We show that adding NH3 to the CO2-H2O binary system induces an efficient absorption of the CO2 in the liquid phase and thus a lower CO2 partial pressure in the vapor phase. Indeed, the CO2 partial pressure remains low for the CO2/NH3 ratio of liquid concentrations lower than 0.5.Assuming various initial compositions of Titan's global water ocean, we explore the thermal and compositional evolution of a massive primitive atmosphere using the thermodynamical model. We are currently investigating how a massive atmosphere may be generated during the satellite growth and how it may then evolve toward a composition dominated by N2. Applications to ocean planets will also be presented at the conference.

Elevated carbon dioxide alters the plasma composition and behaviour of a shark.

PubMed

Green, Leon; Jutfelt, Fredrik

2014-09-01

Increased carbon emissions from fossil fuels are increasing the pCO2 of the ocean surface waters in a process called ocean acidification. Elevated water pCO2 can induce physiological and behavioural effects in teleost fishes, although there appear to be large differences in sensitivity between species. There is currently no information available on the possible responses to future ocean acidification in elasmobranch fishes. We exposed small-spotted catsharks (Scyliorhinus canicula) to either control conditions or a year 2100 scenario of 990 μatm pCO2 for four weeks. We did not detect treatment effects on growth, resting metabolic rate, aerobic scope, skin denticle ultrastructure or skin denticle morphology. However, we found that the elevated pCO2 group buffered internal acidosis via [Formula: see text] accumulation with an associated increase in Na(+), indicating that the blood chemistry remained altered despite the long acclimation period. The elevated pCO2 group also exhibited a shift in their nocturnal swimming pattern from a pattern of many starts and stops to more continuous swimming. Although CO2-exposed teleost fishes can display reduced behavioural asymmetry (lateralization), the CO2-exposed sharks showed increased lateralization. These behavioural effects may suggest that elasmobranch neurophysiology is affected by CO2, as in some teleosts, or that the sharks detect CO2 as a constant stressor, which leads to altered behaviour. The potential direct effects of ocean acidification should henceforth be considered when assessing future anthropogenic effects on sharks. © 2014 The Author(s) Published by the Royal Society. All rights reserved.

Systemic to Microscale Response of Orbicella faveolata to Future Ocean CO2 Conditions.

NASA Astrophysics Data System (ADS)

Dungan, A.; Hall, E. R.; Blackwelder, P. L.; Fogarty, N. D.

2016-02-01

Coral reefs are one of the most economically important ecosystems on the planet, supplying roughly $30 billion USD annually into world economies from the goods and services they provide. Despite their great contributions, anthropogenic influence via carbon dioxide emissions is leading to unprecedented changes in the tropical oceans with concerns about subsequent negative impacts on reefs. Surface ocean pH has dropped 0.1 units in the past century, representing a thirty percent increase in hydrogen ion concentration. In spite of this rapid shift in oceanic chemistry, it is unclear how adult corals and their new recruits will be impacted. In this experiment we examined the relationship between CO2-induced seawater acidification, net calcification, and physiological parameters in Orbicella faveolata adults and new recruits under ambient (465 ± 5.52 ppm), and high (1451 ± 6.51 ppm) CO2 conditions. These treatments represented current and end of the century CO2 values predicted under the RCP8.5 scenario developed by the Intergovernmental Panel on Climate Change (IPCC). Electron microscopy (TEM/SEM) was used to examine coral cellular ultrastructure and newly formed aragonite skeletal crystal structures. Orbicella faveolata exhibited no significant difference in skeletal deposition rates under control and high CO2 conditions; however, crystal formations for both adult and juvenile O. faveolata were statistically longer in the high CO2 treatment. No significant differences were seen in photosynthesis or respiration rates. These results suggest that the addition of CO2 may cause a shift in the overall energy budgets causing a modification of skeletal aragonite crystal structures, rather than inhibiting skeletal crystal formation. Consequential to this energy shift, Orbicella faveolata belongs in the category of Scleractinian corals that exhibit a low sensitivity to ocean acidification and existing colonies may continue to calcify and build reefs in the face of ocean acidification. It remains unclear, however, what the long term effects of a more acidic ocean may be on gamete production and other energy expensive processes.

Natural ocean carbon cycle sensitivity to parameterizations of the recycling in a climate model

NASA Astrophysics Data System (ADS)

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

2014-02-01

Sensitivities of the oceanic biological pump within the GISS (Goddard Institute for Space Studies ) climate modeling system are explored here. Results are presented from twin control simulations of the air-sea CO2 gas exchange using two different ocean models coupled to the same atmosphere. The two ocean models (Russell ocean model and Hybrid Coordinate Ocean Model, HYCOM) use different vertical coordinate systems, and therefore different representations of column physics. Both variants of the GISS climate model are coupled to the same ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM), which computes prognostic distributions for biotic and abiotic fields that influence the air-sea flux of CO2 and the deep ocean carbon transport and storage. In particular, the model differences due to remineralization rate changes are compared to differences attributed to physical processes modeled differently in the two ocean models such as ventilation, mixing, eddy stirring and vertical advection. GISSEH(GISSER) is found to underestimate mixed layer depth compared to observations by about 55% (10%) in the Southern Ocean and overestimate it by about 17% (underestimate by 2%) in the northern high latitudes. Everywhere else in the global ocean, the two models underestimate the surface mixing by about 12-34%, which prevents deep nutrients from reaching the surface and promoting primary production there. Consequently, carbon export is reduced because of reduced production at the surface. Furthermore, carbon export is particularly sensitive to remineralization rate changes in the frontal regions of the subtropical gyres and at the Equator and this sensitivity in the model is much higher than the sensitivity to physical processes such as vertical mixing, vertical advection and mesoscale eddy transport. At depth, GISSER, which has a significant warm bias, remineralizes nutrients and carbon faster thereby producing more nutrients and carbon at depth, which eventually resurfaces with the global thermohaline circulation especially in the Southern Ocean. Because of the reduced primary production and carbon export in GISSEH compared to GISSER, the biological pump efficiency, i.e., the ratio of primary production and carbon export at 75 m, is half in the GISSEH of that in GISSER, The Southern Ocean emerges as a key region where the CO2 flux is as sensitive to biological parameterizations as it is to physical parameterizations. The fidelity of ocean mixing in the Southern Ocean compared to observations is shown to be a good indicator of the magnitude of the biological pump efficiency regardless of physical model choice.

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

NASA Technical Reports Server (NTRS)

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

2014-01-01

Sensitivities of the oceanic biological pump within the GISS (Goddard Institute for Space Studies ) climate modeling system are explored here. Results are presented from twin control simulations of the air-sea CO2 gas exchange using two different ocean models coupled to the same atmosphere. The two ocean models (Russell ocean model and Hybrid Coordinate Ocean Model, HYCOM) use different vertical coordinate systems, and therefore different representations of column physics. Both variants of the GISS climate model are coupled to the same ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM), which computes prognostic distributions for biotic and abiotic fields that influence the air-sea flux of CO2 and the deep ocean carbon transport and storage. In particular, the model differences due to remineralization rate changes are compared to differences attributed to physical processes modeled differently in the two ocean models such as ventilation, mixing, eddy stirring and vertical advection. GISSEH(GISSER) is found to underestimate mixed layer depth compared to observations by about 55% (10 %) in the Southern Ocean and overestimate it by about 17% (underestimate by 2%) in the northern high latitudes. Everywhere else in the global ocean, the two models underestimate the surface mixing by about 12-34 %, which prevents deep nutrients from reaching the surface and promoting primary production there. Consequently, carbon export is reduced because of reduced production at the surface. Furthermore, carbon export is particularly sensitive to remineralization rate changes in the frontal regions of the subtropical gyres and at the Equator and this sensitivity in the model is much higher than the sensitivity to physical processes such as vertical mixing, vertical advection and mesoscale eddy transport. At depth, GISSER, which has a significant warm bias, remineralizes nutrients and carbon faster thereby producing more nutrients and carbon at depth, which eventually resurfaces with the global thermohaline circulation especially in the Southern Ocean. Because of the reduced primary production and carbon export in GISSEH compared to GISSER, the biological pump efficiency, i.e., the ratio of primary production and carbon export at 75 m, is half in the GISSEH of that in GISSER, The Southern Ocean emerges as a key region where the CO2 flux is as sensitive to biological parameterizations as it is to physical parameterizations. The fidelity of ocean mixing in the Southern Ocean compared to observations is shown to be a good indicator of the magnitude of the biological pump efficiency regardless of physical model choice.

Enrichment of Extracellular Carbonic Anhydrase in the Sea Surface Microlayer and Its Effect on Air-Sea CO2 Exchange

NASA Astrophysics Data System (ADS)

Mustaffa, N. I. H.; Striebel, M.; Wurl, O.

2017-12-01

This paper describes the quantification of extracellular carbonic anhydrase (eCA) concentrations in the sea surface microlayer (SML), the boundary layer between the ocean and the atmosphere of the Indo-West Pacific. We demonstrated that the SML is enriched with eCA by 1.5 ± 0.7 compared to the mixed underlying water. Enrichment remains up to a wind speed of 7 m s-1 (i.e., under typical oceanic conditions). As eCA catalyzes the interconversion of HCO3- and CO2, it has been hypothesized that its enrichment in the SML enhances the air-sea CO2 exchange. We detected concentrations in the range of 0.12 to 0.76 nM, which can enhance the exchange by up to 15% based on the model approach described in the literature.

Large-Scale Ocean Circulation-Cloud Interactions Reduce the Pace of Transient Climate Change

NASA Technical Reports Server (NTRS)

Trossman, D. S.; Palter, J. B.; Merlis, T. M.; Huang, Y.; Xia, Y.

2016-01-01

Changes to the large scale oceanic circulation are thought to slow the pace of transient climate change due, in part, to their influence on radiative feedbacks. Here we evaluate the interactions between CO2-forced perturbations to the large-scale ocean circulation and the radiative cloud feedback in a climate model. Both the change of the ocean circulation and the radiative cloud feedback strongly influence the magnitude and spatial pattern of surface and ocean warming. Changes in the ocean circulation reduce the amount of transient global warming caused by the radiative cloud feedback by helping to maintain low cloud coverage in the face of global warming. The radiative cloud feedback is key in affecting atmospheric meridional heat transport changes and is the dominant radiative feedback mechanism that responds to ocean circulation change. Uncertainty in the simulated ocean circulation changes due to CO2 forcing may contribute a large share of the spread in the radiative cloud feedback among climate models.

Analysis of uncertainties in GOSAT-inferred regional CO2 fluxes

NASA Astrophysics Data System (ADS)

Ishizawa, M.; Shirai, T.; Maksyutov, S. S.; Yoshida, Y.; Morino, I.; Inoue, M.; Nakatsuru, T.; Uchino, O.; Mabuchi, K.

2016-12-01

Satellite-based CO2 measurements have potential for improving our understanding global carbon cycle because of more spatiotemporal coverage than those from ground-based observations. Since the Greenhouse gases Observing Satellite (GOSAT) was launched in January 2009, it has been measuring the column-average dry air-mole function of CO2 (XCO2) from the space. To utilize the GOSAT XCO2 for better CO2 flux estimates, several challenges should be overcome. Systematic errors (biases) in XCO2 retrievals are a major factor which leads to large differences among inverted CO2 fluxes. Temporally variable data coverage and density are also taken into account when interpreting the estimated surface fluxes. In this study, we employ an atmospheric inverse model to investigate the impacts of retrievals biases and temporally varying global distribution of GOSAT XCO2 on surface CO2 flux estimates. Inversions are performed for 2009-2013, with several subsets of the 5-year record of GOSAT XCO2 (v2.21) and its bias-corrected XCO2. GOSAT XCO2 data consist of three types: H-gain for vegetated lands, M-gain for bright surfaces (desert areas), and sun-glint for ocean surface. The results show that the global spatial distributions of estimated CO2 fluxes depend on the subset of XCO2 used. M-gain XCO2 results in unrealistically high CO2 emissions in and around the Middle East, including the neighboring ocean regions. On the other hand, M-gain XCO2 causes compensating unrealistic uptakes far beyond M-gain regions in low latitudes, also partially contributing on the summer uptake in Europe. The joint inversions with both surface measurements and GOSAT XCO2 data obtain larger flux gradient between the northern extra-tropics and the tropics than the inversion with surface measurements only for the first 2 years. Recently, these North-South gradients seem to be gradually reducing as the tropics become a weaker source or turn into a sink, while the net emission strength in East Asia is increasing. The 5-year XCO2 data allows us detailed analysis of uncertainties in GOSAT-inferred fluxes and assessment of GOSAT XCO2 biases.

Response of a comprehensive climate model to a broad range of external forcings: relevance for deep ocean ventilation and the development of late Cenozoic ice ages

NASA Astrophysics Data System (ADS)

Galbraith, Eric; de Lavergne, Casimir

2018-03-01

Over the past few million years, the Earth descended from the relatively warm and stable climate of the Pliocene into the increasingly dramatic ice age cycles of the Pleistocene. The influences of orbital forcing and atmospheric CO2 on land-based ice sheets have long been considered as the key drivers of the ice ages, but less attention has been paid to their direct influences on the circulation of the deep ocean. Here we provide a broad view on the influences of CO2, orbital forcing and ice sheet size according to a comprehensive Earth system model, by integrating the model to equilibrium under 40 different combinations of the three external forcings. We find that the volume contribution of Antarctic (AABW) vs. North Atlantic (NADW) waters to the deep ocean varies widely among the simulations, and can be predicted from the difference between the surface densities at AABW and NADW deep water formation sites. Minima of both the AABW-NADW density difference and the AABW volume occur near interglacial CO2 (270-400 ppm). At low CO2, abundant formation and northward export of sea ice in the Southern Ocean contributes to very salty and dense Antarctic waters that dominate the global deep ocean. Furthermore, when the Earth is cold, low obliquity (i.e. a reduced tilt of Earth's rotational axis) enhances the Antarctic water volume by expanding sea ice further. At high CO2, AABW dominance is favoured due to relatively warm subpolar North Atlantic waters, with more dependence on precession. Meanwhile, a large Laurentide ice sheet steers atmospheric circulation as to strengthen the Atlantic Meridional Overturning Circulation, but cools the Southern Ocean remotely, enhancing Antarctic sea ice export and leading to very salty and expanded AABW. Together, these results suggest that a `sweet spot' of low CO2, low obliquity and relatively small ice sheets would have poised the AMOC for interruption, promoting Dansgaard-Oeschger-type abrupt change. The deep ocean temperature and salinity simulated under the most representative `glacial' state agree very well with reconstructions from the Last Glacial Maximum (LGM), which lends confidence in the ability of the model to estimate large-scale changes in water-mass geometry. The model also simulates a circulation-driven increase of preformed radiocarbon reservoir age, which could explain most of the reconstructed LGM-preindustrial ocean radiocarbon change. However, the radiocarbon content of the simulated glacial ocean is still higher than reconstructed for the LGM, and the model does not reproduce reconstructed LGM deep ocean oxygen depletions. These ventilation-related disagreements probably reflect unresolved physical aspects of ventilation and ecosystem processes, but also raise the possibility that the LGM ocean circulation was not in equilibrium. Finally, the simulations display an increased sensitivity of both surface air temperature and AABW volume to orbital forcing under low CO2. We suggest that this enhanced orbital sensitivity contributed to the development of the ice age cycles by amplifying the responses of climate and the carbon cycle to orbital forcing, following a gradual downward trend of CO2.

Impact of Ocean Acidification on Fluxes of non-CO2 Climate-Active Species: Report from the GESAMP WG38 workshop

NASA Astrophysics Data System (ADS)

Suntharalingam, Parvadha; Gehlen, Marion; Hopkins, Frances; Duce, Robert; Jickells, Tim; Gesamp WG38 Workshop, Participants

2017-04-01

Most investigations of the impact of ocean acidification (OA) have focused on changes in oceanic uptake of anthropogenic CO2, the resulting shifts in carbonate chemical equilibria, and the consequences for marine calcifying organisms. Little attention has been paid to the direct impacts of OA on the ocean sources of a range of other gaseous and aerosol species that are influential in regulating radiative forcing, atmospheric oxidising capacity and atmospheric chemistry. The oceanic processes governing emissions of these species are frequently sensitive to the changes in pH and ocean pCO2 accompanying ocean acidification. Such processes include, for example, metabolic rates of microbial activity, levels of surface primary production, ecosystem composition, and photo-chemical and microbially mediated production/loss pathways for individual species. The direct and indirect influences of these factors on oceanic fluxes of non-CO2 trace-gases and aerosols, and the subsequent feedbacks to climate remain highly uncertain. To address these issues UN/GESAMP Working Group 38, The Atmospheric Input of Chemicals to the Ocean, convened a workshop on this topic at the University of East Anglia in February, 2017. The goals of this workshop are to review and synthesize the current science on the direct impacts of ocean acidification on marine emissions to the atmosphere of key species important for climate, and atmospheric chemistry; and to identify the primary needs for new research to improve process understanding and to quantify the impact of ocean acidification on these marine fluxes (i.e., provide recommendations on the specific laboratory process studies, field measurements and model analyses needed to support targeted research activities on this topic). The results, conclusions, and recommendations of this workshop will be presented.

The Phenomenom of Ocean Acidification

NASA Astrophysics Data System (ADS)

Weiss, S.

2017-12-01

The earth is 70% and is protected by its atmosphere. The atmosphere is made up of several layers. The sunlight penetrates through the atmosphere and warms the earth surface. The earth's surface then in turn emits invisible infrared radiation back. As this radiation moves back up each layer absorbs some of it. Each layer then sends some of this energy back to earth again. When the layer becomes so thin the energy then escapes back into space. When we are adding more carbon dioxide to these layers we are causing the layers to absorb more of the energy and the radiation. This in turn causes the layers to become warmer since fewer radiation moves up through the layers and this energy bounces back to earth increasing the temperatures. The entire planet is taking on more of this energy and hence the temperatures are rising. The ocean plays a big rule in this change. It has prevented some of the CO2 from entering the earth's atmosphere. Oceans absorb about one third of the anthropogenic CO2 causing the phenomenon of ocean acidification and this comes at a huge cost to our marine environments. The CO2 is absorbed on the surface and then transferred into the deeper waters. Which causes it to be stuck for centuries before making its way back into the atmosphere. As the CO2 dissolves in seawater it causes the PH to lower. With a lowered PH water becomes more acidic. The Hydrogen ions decrease and become less active. With this process carbonic acid is formed. The ocean now is more acidic then it has ever been in the past 650,000 years. The increase in acidic levels has caused our marine life to adjust. Acidosis caused by the increase of carbonic acid in the body fluids means a lower pH in the blood. This changes is just the start to many health issues for these organism's.

Kinetic bottlenecks to chemical exchange rates for deep-sea animals II: Carbon dioxide

NASA Astrophysics Data System (ADS)

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

2012-11-01

Increased 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. Discussion of these impacts has so far focused only on changes in the oceanic bulk fluid properties (ΔpH, Δ[∑CO2] etc.) as the critical variable and with a major focus on carbonate shell dissolution. Here we describe the rate problem for animals that 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 layer around marine animals in an ocean changing in temperature (T) and CO2 concentration 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--CO32- acid-base system needs to be considered. These reactions significantly facilitate CO2 efflux compared to O2 intake at equal temperature, pressure and flow rate under typical oceanic concentrations.The effect of these reactions can be described by an enhancement factor. For organisms, this means mechanically increasing flow over their surface to thin the boundary layer as is required to alleviate O2 stress seems not necessary to facilitate CO2 efflux. Nevertheless the elevated pCO2 cost most likely is non-zero. 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, for the problem of gas exchange with the bulk ocean, the combination of an increasing T combined with declining O2 poses a greater 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.

Mixotrophic basis of Atlantic oligotrophic ecosystems.

PubMed

Hartmann, Manuela; Grob, Carolina; Tarran, Glen A; Martin, Adrian P; Burkill, Peter H; Scanlan, David J; Zubkov, Mikhail V

2012-04-10

Oligotrophic subtropical gyres are the largest oceanic ecosystems, covering >40% of the Earth's surface. Unicellular cyanobacteria and the smallest algae (plastidic protists) dominate CO(2) fixation in these ecosystems, competing for dissolved inorganic nutrients. Here we present direct evidence from the surface mixed layer of the subtropical gyres and adjacent equatorial and temperate regions of the Atlantic Ocean, collected on three Atlantic Meridional Transect cruises on consecutive years, that bacterioplankton are fed on by plastidic and aplastidic protists at comparable rates. Rates of bacterivory were similar in the light and dark. Furthermore, because of their higher abundance, it is the plastidic protists, rather than the aplastidic forms, that control bacterivory in these waters. These findings change our basic understanding of food web function in the open ocean, because plastidic protists should now be considered as the main bacterivores as well as the main CO(2) fixers in the oligotrophic gyres.

Why Do Organisms in the Atlantic Ocean Produce So Much CaCO3?

NASA Astrophysics Data System (ADS)

Toggweiler, J. R.

2010-12-01

Sediments in the Atlantic are richer in CaCO3 than sediments in the other oceans. Sediment trap observations show that sinking particles in the Atlantic also tend to have more CaCO3 in relation to organic carbon than sinking particles elsewhere. The reason for the extra production of CaCO3 has never been very clear. The Atlantic is unusual because it receives much more than its share of the global input of river water. River water adds alkalinity to the surface ocean while the production of CaCO3 takes it away. In this presentation a new tracer, called Alk*, is derived from the surface alkalinity distribution to highlight the impact of river inputs and the production of CaCO3. If the production of CaCO3 were evenly distributed across the ocean one would expect the Atlantic to have a higher level of Alk* becaused of its river inputs. We find instead that Alk* is lower in the middle of the Atlantic than almost any place else. This, of course, is consistent with the fact that organisms in the Atlantic produce a lot of CaCO3. Comparison with other areas with especially low values of Alk* (Red Sea and northern Arabian Sea) shows that the production of CaCO3 is highly correlated across the ocean with the surface salinity. Hence, we argue that organisms in the Atlantic produce a lot of CaCO3 simply because the Atlantic is so salty. Salty waters, by definition, have more CO3= ions, which increase the supersaturation with respect to calcite and aragonite. This finding, while extremely simple, has major implifications for the impact of ocean acidification on calcifying organisms.

Climate, ocean circulation, and sea level changes under stabilization and overshoot pathways to 1.5 K warming

NASA Astrophysics Data System (ADS)

Palter, Jaime B.; Frölicher, Thomas L.; Paynter, David; John, Jasmin G.

2018-06-01

The Paris Agreement has initiated a scientific debate on the role that carbon removal - or net negative emissions - might play in achieving less than 1.5 K of global mean surface warming by 2100. Here, we probe the sensitivity of a comprehensive Earth system model (GFDL-ESM2M) to three different atmospheric CO2 concentration pathways, two of which arrive at 1.5 K of warming in 2100 by very different pathways. We run five ensemble members of each of these simulations: (1) a standard Representative Concentration Pathway (RCP4.5) scenario, which produces 2 K of surface warming by 2100 in our model; (2) a stabilization pathway in which atmospheric CO2 concentration never exceeds 440 ppm and the global mean temperature rise is approximately 1.5 K by 2100; and (3) an overshoot pathway that passes through 2 K of warming at mid-century, before ramping down atmospheric CO2 concentrations, as if using carbon removal, to end at 1.5 K of warming at 2100. Although the global mean surface temperature change in response to the overshoot pathway is similar to the stabilization pathway in 2100, this similarity belies several important differences in other climate metrics, such as warming over land masses, the strength of the Atlantic Meridional Overturning Circulation (AMOC), ocean acidification, sea ice coverage, and the global mean sea level change and its regional expressions. In 2100, the overshoot ensemble shows a greater global steric sea level rise and weaker AMOC mass transport than in the stabilization scenario, with both of these metrics close to the ensemble mean of RCP4.5. There is strong ocean surface cooling in the North Atlantic Ocean and Southern Ocean in response to overshoot forcing due to perturbations in the ocean circulation. Thus, overshoot forcing in this model reduces the rate of sea ice loss in the Labrador, Nordic, Ross, and Weddell seas relative to the stabilized pathway, suggesting a negative radiative feedback in response to the early rapid warming. Finally, the ocean perturbation in response to warming leads to strong pathway dependence of sea level rise in northern North American cities, with overshoot forcing producing up to 10 cm of additional sea level rise by 2100 relative to stabilization forcing.

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

PubMed

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

2013-09-01

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

Comparison of Carbon Dioxide Airborne Measurement over Land and Ocean using 2-μm Double-Pulse Integrated Path Differential Absorption Lidar

NASA Astrophysics Data System (ADS)

Refaat, T. F.; Singh, U. N.; Petros, M.; Yu, J.; Remus, R.; Ismail, S.

2017-12-01

An airborne Integrated Path Differential Absorption (IPDA) lidar has been developed and validated at NASA Langley Research Center for atmospheric carbon dioxide column measurements. The instrument consists of a tunable, high-energy 2-μm double pulse laser transmitter and 0.4 m telescope receiver coupled to an InGaAs pin detection system. The instrument was validated for carbon dioxide (CO2) measurements from ground and airborne platforms, using a movable lidar trailer and the NASA B-200 aircraft. Airborne validation was conducted over the ocean by comparing the IPDA CO2 optical depth measurement to optical depth model derived using NOAA airborne CO2 air-sampling. Another airborne validation was conducted over land vegetation by comparing the IPDA measurement to a model derived using on-board in-situ measurements using an absolute, non-dispersive infrared gas analyzer (LiCor 840A). IPDA range measurements were also compared to rangefinder and Global Positioning System (GPS) records during ground and airborne validation, respectively. Range measurements from the ground indicated a 0.93 m IPDA range measurement uncertainty, which is limited by the transmitted laser pulse and detection system properties. This uncertainty increased to 2.80 and 7.40 m over ocean and land, due to fluctuations in ocean surface and ground elevations, respectively. IPDA CO2 differential optical depth measurements agree with both models. Consistent CO2 optical depth biases were well correlated with the digitizer full scale input range settings. CO2 optical depth measurements over ocean from 3.1 and 6.1 km altitudes indicated 0.95% and 0.83% uncertainty, respectively, using 10 second (100 shots) averaging. Using the same averaging 0.40% uncertainty was observed over land, from 3.4 km altitude, due to higher surface reflectivity, which increases the return signal power and enhances the signal-to-noise ratio. However, less uncertainty is observed at higher altitudes due to reduced signal shot noise, indicating that detection system noise-equivalent-power dominates the error. These results show that the IPDA technique is well suited for space-based platforms, which includes larger column content integration that enhances the measurement sensitivity.

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

USGS Publications Warehouse

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

2010-01-01

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

Effects of ocean acidification, warming and melting of sea ice on aragonite saturation of the Canada Basin surface water

NASA Astrophysics Data System (ADS)

Yamamoto-Kawai, M.; McLaughlin, F. A.; Carmack, E. C.

2011-02-01

In 2008, surface waters in the Canada Basin of the Arctic Ocean were found to be undersaturated with respect to aragonite. This is associated with recent extensive melting of sea ice in this region, as well as elevated sea surface temperature and atmospheric CO2 concentrations. We have estimated the relative contribution of each of these controlling factors to the calcium carbonate saturation state (Ω) from observations of dissolved inorganic carbon, total alkalinity and oxygen isotope ratio. Results indicate that the increase in atmospheric CO2 has lowered surface Ω by ˜0.3 in the Canada Basin since the preindustrial period. Recent melting of sea ice has further lowered mean Ω by 0.4, and of this, half was due to dilution of surface water and half was due to the change in air-sea disequilibrium state. Surface water warming has generally counteracted the mean decrease in Ω by 0.1.

Risk maps for Antarctic krill under projected Southern Ocean acidification

NASA Astrophysics Data System (ADS)

Kawaguchi, S.; Ishida, A.; King, R.; Raymond, B.; Waller, N.; Constable, A.; Nicol, S.; Wakita, M.; Ishimatsu, A.

2013-09-01

Marine ecosystems of the Southern Ocean are particularly vulnerable to ocean acidification. Antarctic krill (Euphausia superba; hereafter krill) is the key pelagic species of the region and its largest fishery resource. There is therefore concern about the combined effects of climate change, ocean acidification and an expanding fishery on krill and ultimately, their dependent predators--whales, seals and penguins. However, little is known about the sensitivity of krill to ocean acidification. Juvenile and adult krill are already exposed to variable seawater carbonate chemistry because they occupy a range of habitats and migrate both vertically and horizontally on a daily and seasonal basis. Moreover, krill eggs sink from the surface to hatch at 700-1,000m (ref. ), where the carbon dioxide partial pressure (pCO2) in sea water is already greater than it is in the atmosphere. Krill eggs sink passively and so cannot avoid these conditions. Here we describe the sensitivity of krill egg hatch rates to increased CO2, and present a circumpolar risk map of krill hatching success under projected pCO2 levels. We find that important krill habitats of the Weddell Sea and the Haakon VII Sea to the east are likely to become high-risk areas for krill recruitment within a century. Furthermore, unless CO2 emissions are mitigated, the Southern Ocean krill population could collapse by 2300 with dire consequences for the entire ecosystem.

A 1-D model of sinking particles

NASA Astrophysics Data System (ADS)

Jokulsdottir, T.; Archer, D.

2006-12-01

Acidification of the surface ocean due to increased atmospheric CO2 levels is altering its saturation state with respect to calcium carbonate (Orr et al., 2005) and the ability of calcifying phytoplankton to calcify (Riebesell et al., 2000). Sequestration of atmospheric carbon dioxide into the deep ocean is affected by this, because calcite is the key component in ballasting sinking particles (Klaas and Archer, 2001). The settling velocity of particles is not explicitly modeled but often represented as a constant in climate models. That is clearly inaccurate as the composition of particles changes with depth as bacteria and dissolution processes act on its different components, changing their ratio with depth. An idealized, mechanistic model of particles has been developed where settling velocity is calculated from first principles. The model is forced 100m below the surface with export ratios (organic carbon/calcium carbonate) corresponding to different CO2 levels according to Riebesell et al. The resulting flux is compared to the flux generated by the same model where the settling velocity is held constant. The model produces a relatively constant rain ratio regardless of the amount of calcite available to ballast the particle, which is what data suggests (Conte et al., 2001), whereas a constant velocity model does not. Comparing the flux of particulate organic carbon to the seafloor with increasing CO2 levels, the outcome of the constant velocity model is an increase whereas when the velocity is calculated a decrease results. If so, the change in export ratio with an increase in CO2 concentrations acts as a positive feedback: as increased atmospheric CO2 levels lead to the ocean pH being lowered, reduced calcification of marine organisms results and a decrease in particulate organic carbon flux to the deep ocean, which again raises CO2 concentrations. Conte, M.,, N. Ralph, E. Ross, Seasonal and interannual variability in deep ocean particle fluxes at the Oceanic Flux Program (OFP)/Bermuda Atlantic Time Series (BATS) site in the western Sargasso Sea near Bermuda, Deep-Sea Research II 48 1471-1505, 2001 Klaas, C., and D.E. Archer, Association of sinking organic matter with various types of mineral ballast in the deep sea: Implications for the rain ratio, Global Biogeochemical Cycles, 16, 2002. Orr, J. C. and et. al. Anthropogenic ocean acidification over calcifying organisms. Nature, 437(29):681 686, 2005. U. Riebesell, I. Zondervan, B. Rost, P.D. Tortell, R.E. Zeebe, and F.M.M.Morel. Reduced calcification of marine plankton in response to increased atmospheric CO2. Nature, 407:364 368, 2000.

Decoupling of coral skeletal δ13C and solar irradiance over the past millennium caused by the oceanic Suess effect

NASA Astrophysics Data System (ADS)

Deng, Wenfeng; Chen, Xuefei; Wei, Gangjian; Zeng, Ti; Zhao, Jian-xin

2017-02-01

Many factors influence the seasonal changes in δ13C levels in coral skeletons; consequently, the climatic and environmental significance of such changes is complicated and controversial. However, it is widely accepted that the secular declining trend of coral δ13C over the past 200 years reflects the changes in the additional flux of anthropogenic CO2 from the atmosphere into the surface oceans. Even so, the centennial-scale variations, and their significance, of coral δ13C before the Industrial Revolution remain unclear. Based on an annually resolved coral δ13C record from the northern South China Sea, the centennial-scale variations of coral δ13C over the past millennium were studied. The coral δ13C and total solar irradiance (TSI) have a significant positive Pearson correlation and coupled variation during the Medieval Warm Period and Little Ice Age, when natural forcing controlled the climate and environment. This covariation suggests that TSI controls coral δ13C by affecting the photosynthetic activity of the endosymbiotic zooxanthellae over centennial timescales. However, there was a decoupling of the coral skeletal δ13C and TSI during the Current Warm Period, the period in which the climate and environment became linked to anthropogenic factors. Instead, coral δ13C levels have a significant Pearson correlation with both the atmospheric CO2 concentration and δ13C levels in atmospheric CO2. The correlation between coral δ13C and atmospheric CO2 suggests that the oceanic 13C Suess effect, caused by the addition of increasing amounts of anthropogenic 12CO2 to the surface ocean, has led to the decoupling of coral δ13C and TSI at the centennial scale.

Estimating surface pCO2 in the northern Gulf of Mexico: Which remote sensing model to use?

NASA Astrophysics Data System (ADS)

Chen, Shuangling; Hu, Chuanmin; Cai, Wei-Jun; Yang, Bo

2017-12-01

Various approaches and models have been proposed to remotely estimate surface pCO2 in the ocean, with variable performance as they were designed for different environments. Among these, a recently developed mechanistic semi-analytical approach (MeSAA) has shown its advantage for its explicit inclusion of physical and biological forcing in the model, yet its general applicability is unknown. Here, with extensive in situ measurements of surface pCO2, the MeSAA, originally developed for the summertime East China Sea, was tested in the northern Gulf of Mexico (GOM) where river plumes dominate water's biogeochemical properties during summer. Specifically, the MeSAA-predicted surface pCO2 was estimated by combining the dominating effects of thermodynamics, river-ocean mixing and biological activities on surface pCO2. Firstly, effects of thermodynamics and river-ocean mixing (pCO2@Hmixing) were estimated with a two-endmember mixing model, assuming conservative mixing. Secondly, pCO2 variations caused by biological activities (ΔpCO2@bio) was determined through an empirical relationship between sea surface temperature (SST)-normalized pCO2 and MODIS (Moderate Resolution Imaging Spectroradiometer) 8-day composite chlorophyll concentration (CHL). The MeSAA-modeled pCO2 (sum of pCO2@Hmixing and ΔpCO2@bio) was compared with the field-measured pCO2. The Root Mean Square Error (RMSE) was 22.94 μatm (5.91%), with coefficient of determination (R2) of 0.25, mean bias (MB) of - 0.23 μatm and mean ratio (MR) of 1.001, for pCO2 ranging between 316 and 452 μatm. To improve the model performance, a locally tuned MeSAA was developed through the use of a locally tuned ΔpCO2@bio term. A multi-variate empirical regression model was also developed using the same dataset. Both the locally tuned MeSAA and the regression models showed improved performance comparing to the original MeSAA, with R2 of 0.78 and 0.84, RMSE of 12.36 μatm (3.14%) and 10.66 μatm (2.68%), MB of 0.00 μatm and - 0.10 μatm, MR of 1.001 and 1.000, respectively. A sensitivity analysis was conducted to study the uncertainties in the predicted pCO2 as a result of the uncertainties in the input variables of each model. Although the MeSAA was more sensitive to variations in SST and CHL than in sea surface salinity (SSS), and the locally tuned MeSAA and the empirical regression models were more sensitive to changes in SST and SSS than in CHL, generally for these three models the bias induced by the uncertainties in the empirically derived parameters (river endmember total alkalinity (TA) and dissolved inorganic carbon (DIC), biological coefficient of the MeSAA and locally tuned MeSAA models) and environmental variables (SST, SSS, CHL) was within or close to the uncertainty of each model. While all these three models showed that surface pCO2 was positively correlated to SST, the MeSAA showed negative correlation between surface pCO2 and SSS and CHL but the locally tuned MeSAA and the empirical regression showed the opposite. These results suggest that the locally tuned MeSAA worked better in the river-dominated northern GOM than the original MeSAA, with slightly worse statistics but more meaningful physical and biogeochemical interpretations than the empirical regression model. Because data from abnormal upwelling were not used to train the models, they are not applicable for waters with strong upwelling, yet the empirical regression approach showed ability to be further tuned to adapt to such cases.

Species-specific effects of near-future CO2 on the respiratory performance of two tropical prey fish and their predator

PubMed Central

Couturier, Christine S.; Stecyk, Jonathan A. W.; Rummer, Jodie L.; Munday, Philip L.; Nilsson, Göran E.

2013-01-01

Ocean surface CO2 levels are increasing in line with rising atmospheric CO2 and could exceed 900 μatm by year 2100, with extremes above 2000 μatm in some coastal habitats. The imminent increase in ocean pCO2 is predicted to have negative consequences for marine fishes, including reduced aerobic performance, but variability among species could be expected. Understanding interspecific responses to ocean acidification is important for predicting the consequences of ocean acidification on communities and ecosystems. In the present study, the effects of exposure to near-future seawater CO2 (860 μatm) on resting (Ṁ O2rest) and maximum (Ṁ O2max) oxygen consumption rates were determined for three tropical coral reef fish species interlinked through predator-prey relationships: juvenile Pomacentrus moluccensis and P. amboinensis, and one of their predators: adult Pseudochromis fuscus. Contrary to predictions, one of the prey species, P. amboinensis, displayed a 28 – 39 % increase in Ṁ O2max after both an acute and four-day exposure to near-future CO2 seawater, while maintaining Ṁ O2rest. By contrast, the same treatment had no significant effects on Ṁ O2rest or Ṁ O2max of the other two species. However, acute exposure of P. amboinensis to 1400 and 2400 μatm CO2 resulted in Ṁ O2max returning to control values. Overall, the findings suggest that: (1) the metabolic costs of living in a near-future CO2 seawater environment were insignificant for the species examined at rest; (2) the ṀO2max response of tropical reef species to near-future CO2 seawater can be dependent on the severity of external hypercapnia; and (3) near-future ocean pCO2 may not be detrimental to aerobic scope of all fish species and it may even augment aerobic scope of some species. The present results also highlight that close phylogenetic relatedness and living in the same environment, does not necessarily imply similar physiological responses to near-future CO2. PMID:23916817

Multi-scale modeling of CO2 dispersion leaked from seafloor off the Japanese coast.

PubMed

Kano, Yuki; Sato, Toru; Kita, Jun; Hirabayashi, Shinichiro; Tabeta, Shigeru

2010-02-01

A numerical simulation was conducted to predict the change of pCO(2) in the ocean caused by CO(2) leaked from an underground aquifer, in which CO(2) is purposefully stored. The target space of the present model was the ocean above the seafloor. The behavior of CO(2) bubbles, their dissolution, and the advection-diffusion of dissolved CO(2) were numerically simulated. Here, two cases for the leakage rate were studied: an extreme case, 94,600 t/y, which assumed that a large fault accidentally connects the CO(2) reservoir and the seafloor; and a reasonable case, 3800 t/y, based on the seepage rate of an existing EOR site. In the extreme case, the calculated increase in DeltapCO(2) experienced by floating organisms was less than 300 ppm, while that for immobile organisms directly over the fault surface periodically exceeded 1000 ppm, if momentarily. In the reasonable case, the calculated DeltapCO(2) and pH were within the range of natural fluctuation. Copyright 2009 Elsevier Ltd. All rights reserved.

Influence of elevated CO2 concentrations on cell division and nitrogen fixation rates in the bloom-forming cyanobacterium Nodularia spumigena

NASA Astrophysics Data System (ADS)

Czerny, J.; Ramos, J. Barcelos E.; Riebesell, U.

2009-09-01

The surface ocean absorbs large quantities of the CO2 emitted to the atmosphere from human activities. As this CO2 dissolves in seawater, it reacts to form carbonic acid. While this phenomenon, called ocean acidification, has been found to adversely affect many calcifying organisms, some photosynthetic organisms appear to benefit from increasing [CO2]. Among these is the cyanobacterium Trichodesmium, a predominant diazotroph (nitrogen-fixing) in large parts of the oligotrophic oceans, which responded with increased carbon and nitrogen fixation at elevated pCO2. With the mechanism underlying this CO2 stimulation still unknown, the question arises whether this is a common response of diazotrophic cyanobacteria. In this study we therefore investigate the physiological response of Nodularia spumigena, a heterocystous bloom-forming diazotroph of the Baltic Sea, to CO2-induced changes in seawater carbonate chemistry. N. spumigena reacted to seawater acidification/carbonation with reduced cell division rates and nitrogen fixation rates, accompanied by significant changes in carbon and phosphorus quota and elemental composition of the formed biomass. Possible explanations for the contrasting physiological responses of Nodularia compared to Trichodesmium may be found in the different ecological strategies of non-heterocystous (Trichodesmium) and heterocystous (Nodularia) cyanobacteria.

INTERACTIONS BETWEEN OCEAN ACIDIFICATION AND WARMING ON THE MORTALITY AND DISSOLUTION OF CORALLINE ALGAE(1).

PubMed

Diaz-Pulido, Guillermo; Anthony, Kenneth R N; Kline, David I; Dove, Sophie; Hoegh-Guldberg, Ove

2012-02-01

Coralline algae are among the most sensitive calcifying organisms to ocean acidification as a result of increased atmospheric carbon dioxide (pCO2 ). Little is known, however, about the combined impacts of increased pCO2 , ocean acidification, and sea surface temperature on tissue mortality and skeletal dissolution of coralline algae. To address this issue, we conducted factorial manipulative experiments of elevated CO2 and temperature and examined the consequences on tissue survival and skeletal dissolution of the crustose coralline alga (CCA) Porolithon (=Hydrolithon) onkodes (Heydr.) Foslie (Corallinaceae, Rhodophyta) on the southern Great Barrier Reef (GBR), Australia. We observed that warming amplified the negative effects of high pCO2 on the health of the algae: rates of advanced partial mortality of CCA increased from <1% to 9% under high CO2 (from 400 to 1,100 ppm) and exacerbated to 15% under warming conditions (from 26°C to 29°C). Furthermore, the effect of pCO2 on skeletal dissolution strongly depended on temperature. Dissolution of P. onkodes only occurred in the high-pCO2 treatment and was greater in the warm treatment. Enhanced skeletal dissolution was also associated with a significant increase in the abundance of endolithic algae. Our results demonstrate that P. onkodes is particularly sensitive to ocean acidification under warm conditions, suggesting that previous experiments focused on ocean acidification alone have underestimated the impact of future conditions on coralline algae. Given the central role that coralline algae play within coral reefs, these conclusions have serious ramifications for the integrity of coral-reef ecosystems. © 2011 Phycological Society of America.

Sensitivity of Global Sea-Air CO2 Flux to Gas Transfer Algorithms, Climatological Wind Speeds, and Variability of Sea Surface Temperature and Salinity

NASA Technical Reports Server (NTRS)

McClain, Charles R.; Signorini, Sergio

2002-01-01

Sensitivity analyses of sea-air CO2 flux to gas transfer algorithms, climatological wind speeds, sea surface temperatures (SST) and salinity (SSS) were conducted for the global oceans and selected regional domains. Large uncertainties in the global sea-air flux estimates are identified due to different gas transfer algorithms, global climatological wind speeds, and seasonal SST and SSS data. The global sea-air flux ranges from -0.57 to -2.27 Gt/yr, depending on the combination of gas transfer algorithms and global climatological wind speeds used. Different combinations of SST and SSS global fields resulted in changes as large as 35% on the oceans global sea-air flux. An error as small as plus or minus 0.2 in SSS translates into a plus or minus 43% deviation on the mean global CO2 flux. This result emphasizes the need for highly accurate satellite SSS observations for the development of remote sensing sea-air flux algorithms.

Impact of elevated CO2 on shellfish calcification

NASA Astrophysics Data System (ADS)

Gazeau, Frédéric; Quiblier, Christophe; Jansen, Jeroen M.; Gattuso, Jean-Pierre; Middelburg, Jack J.; Heip, Carlo H. R.

2007-04-01

Ocean acidification resulting from human emissions of carbon dioxide has already lowered and will further lower surface ocean pH. The consequent decrease in calcium carbonate saturation potentially threatens calcareous marine organisms. Here, we demonstrate that the calcification rates of the edible mussel (Mytilus edulis) and Pacific oyster (Crassostrea gigas) decline linearly with increasing pCO2. Mussel and oyster calcification may decrease by 25 and 10%, respectively, by the end of the century, following the IPCC IS92a scenario (~740 ppmv in 2100). Moreover, mussels dissolve at pCO2 values exceeding a threshold value of ~1800 ppmv. As these two species are important ecosystem engineers in coastal ecosystems and represent a large part of worldwide aquaculture production, the predicted decrease of calcification in response to ocean acidification will probably have an impact on coastal biodiversity and ecosystem functioning as well as potentially lead to significant economic loss.

Observations of changes in the dissolved CO2 system in the North Sea, in four summers of the 2001-2011 decade

NASA Astrophysics Data System (ADS)

Clargo, Nicola; Salt, Lesley; Thomas, Helmuth; de Baar, Hein

2015-04-01

Since the industrial revolution, atmospheric concentrations of carbon dioxide (CO2) have risen dramatically, largely due to the combustion of fossil fuels, changes in land-use patterns and the production of cement. The oceans have absorbed a large amount of this CO2, with resulting impacts on ocean chemistry. Coastal seas play a significant role in the mitigation of anthropogenic atmospheric CO2 as they contribute approximately 10-30% of global primary productivity despite accounting for only 7% of the surface area. The North Sea is a perfect natural laboratory in which to study the CO2 system as it consists of two biogeochemically distinct regions displaying both oceanic and relatively coastal behaviour. It has also been identified as a continental shelf pump with respect to CO2, transporting it to the deeper waters of the North Atlantic. Large scale forcing has been shown to have a significant impact on the CO2 system over varying time scales, often masking the effects of anthropogenic influence. Here, we present data from the North Sea spanning the 2001-2011 decade. In order to investigate the dynamics of the dissolved CO2 system in this region in the face of climate change, four basin-wide cruises were conducted during the summers of 2001, 2005, 2008 and 2011. The acquired Dissolved Inorganic Carbon (DIC) and alkalinity data were then used to fully resolve the carbon system in order to assess trends over the 2001-2011 decade. We find significant interannual variability, but with a consistent, notable trend in decreasing pH. We found that surface alkalinity remained relatively constant over the decade, whereas DIC increased, indicating that the pH decline is DIC-driven. We also found that the partial pressure of CO2 (pCO2) increased faster than concurrent atmospheric CO2 concentrations, and that the CO2 buffering capacity of the North Sea decreased over the decade, with implications for future CO2 uptake.

Attributing Contributions of Climate Feedbacks to the Seasonal Cycle of Surface Warming due to CO2 Increase

NASA Astrophysics Data System (ADS)

Sejas, S.; Cai, M.

2012-12-01

Surfing warming due to CO2 doubling is a robust feature of coupled general circulation models (GCM), as noted in the IPCC AR4 assessment report. In this study, the contributions of different climate feedbacks to the magnitude, spatial distribution, and seasonality of the surface warming is examined using data from NCAR's CCSM4. In particular, a focus is placed on polar regions to see which feedbacks play a role in polar amplification and its seasonal pattern. A new climate feedback analysis method is used to isolate the surface warming or cooling contributions of both radiative and non-radiative (dynamical) climate feedbacks to the total (actual) surface temperature change given by the CCSM4. These contributions (or partial surface temperature changes) are additive and their total is approximately equal to the actual surface temperature change. What is found is that the effects of CO2 doubling alone warms the surface throughout with a maximum in polar regions, which indicates the CO2 forcing alone has a degree of polar warming amplification. Water vapor feedback is a positive feedback throughout but is most responsible for the surface warming found in the tropics. Polar warming amplification is found to be strongest away from summer (especially in NH), which is primarily caused by a positive feedback due to cloud feedbacks but with the surface temperature change due to the CO2 forcing alone and the ocean dynamics and storage feedback also playing an important role. Contrary to popular belief, surface albedo feedback (SAF) does not account for much of the polar amplification. SAF tries to amplify polar warming, but in summer. No major polar amplification is seen in summer for the actual surface temperature, so SAF is not the feedback responsible for polar amplification. This is actually a consequence of the ocean dynamics and storage feedback, which negates the effects of SAF to a large degree.

Controlling mechanisms of surface partial pressure of CO2 in Jiaozhou Bay during summer and the influence of heavy rain

NASA Astrophysics Data System (ADS)

Li, Yunxiao; Yang, Xufeng; Han, Ping; Xue, Liang; Zhang, Longjun

2017-09-01

Due to the combined effects of natural processes and human activities, carbon source/sink processes and mechanisms in the coastal ocean are becoming more and more important in current ocean carbon cycle research. Based on differences in the ratio of total alkalinity (TA) to dissolved inorganic carbon (DIC) associated with terrestrial input, biological process (production and respiration), calcium carbonate (CaCO3) process (precipitation and dissolution) and CO2 evasion/invasion, we discuss the mechanisms controlling the surface partial pressure of CO2 (pCO2) in Jiaozhou Bay (JZB) during summer and the influence of heavy rain, via three cruises performed in mid-June, early July and late July of 2014. In mid-June and in early July, without heavy rain or obvious river input, sea surface pCO2 ranged from 521 to 1080 μatm and from 547 to 998 μatm, respectively. The direct input of DIC from sewage and the intense respiration produced large DIC additions and the highest pCO2 values in the northeast of the bay near the downtown of Qingdao. However, in the west of the bay, significant CaCO3 precipitation led to DIC removal but no obvious increase in pCO2, which was just close to that in the central area. Due to the shallow depth and longer water residence time in this region, this pattern may be related to the sustained release of CO2 into the atmosphere. In late July, heavy rain promoted river input in the western and eastern portions of JZB. Strong primary production led to a significant decrease in pCO2 in the western area, with the lowest pCO2 value of 252 μatm. However, in the northeastern area, the intense respiration remained, and the highest pCO2 value was 1149 μatm. The average air-sea CO2 flux in mid-June and early July was 20.23 mmol m- 2 d- 1 and 23.56 mmol m- 2 d- 1, respectively. In contrast, in late July, sources became sinks for atmospheric CO2 in the western and central areas of the bay, halving the average air-sea CO2 flux to a value of 10.58 mmol m- 2 d- 1. Therefore, without considering the impact of heavy rains, the estimated air-sea CO2 flux is likely inaccurate in coastal waters. Our study implies that more studies in the coastal ocean are needed to determine the duration and intensity of the CO2 sink after the occurrence of heavy rain as well as the magnitudes of the CO2 sink associated with varying rainfall intensities.

Enceladus' near-surface CO2 gas pockets and surface frost deposits

NASA Astrophysics Data System (ADS)

Matson, Dennis L.; Davies, Ashley Gerard; Johnson, Torrence V.; Combe, Jean-Philippe; McCord, Thomas B.; Radebaugh, Jani; Singh, Sandeep

2018-03-01

Solid CO2 surface deposits were reported in Enceladus' South Polar Region by Brown et al. (2006). They noted that such volatile deposits are temporary and posited ongoing replenishment. We present a model for this replenishment by expanding on the Matson et al. (2012) model of subsurface heat and chemical transport in Enceladus. Our model explains the distributions of both CO2 frost and complexed CO2 clathrate hydrate as seen in the Cassini Visual and Infrared Mapping Spectrometer (VIMS) data. We trace the journey of CO2 from a subsurface ocean. The ocean-water circulation model of Matson et al. (2012) brings water up to near the surface where gas exsolves to form bubbles. Some of the CO2 bubbles are trapped and form pockets of gas in recesses at the bottom of the uppermost ice layer. When fissures break open these pockets, the CO2 gas is vented. Gas pocket venting is episodic compared to the more or less continuous eruptive plumes, emanating from the "tiger stripes", that are supported by plume chambers. Two styles of gas pocket venting are considered: (1) seeps, and (2) blowouts. The presence of CO2 frost patches suggests that the pocket gas slowly seeped through fractured, cold ice and when some of the gas reached the surface it was cold enough to condense (i.e., T ∼70 to ∼119 K). If the fissure opening is large, a blowout occurs. The rapid escape of gas and drop in pocket pressure causes water in the pocket to boil and create many small aerosol droplets of seawater. These may be carried along by the erupting gas. Electrically charged droplets can couple to the magnetosphere, and be dragged away from Enceladus. Most of the CO2 blowout gas escapes from Enceladus and the remainder is distributed globally. However, CO2 trapped in a clathrate structure does not escape. It is much heavier and slower moving than the CO2 gas. Its motion is ballistic and has an average range of about 17 km. Thus, it contributes to deposits in the vicinity of the vent. Local heat flow indicates that gas pockets can be located as deep as several tens of meters below the surface. Gas pockets can be reused, and we explore their life cycle.

Calcification response of a key phytoplankton family to millennial-scale environmental change.

PubMed

McClelland, H L O; Barbarin, N; Beaufort, L; Hermoso, M; Ferretti, P; Greaves, M; Rickaby, R E M

2016-09-28

Coccolithophores are single-celled photosynthesizing marine algae, responsible for half of the calcification in the surface ocean, and exert a strong influence on the distribution of carbon among global reservoirs, and thus Earth's climate. Calcification in the surface ocean decreases the buffering capacity of seawater for CO 2 , whilst photosynthetic carbon fixation has the opposite effect. Experiments in culture have suggested that coccolithophore calcification decreases under high CO 2 concentrations ([CO 2 (aq)]) constituting a negative feedback. However, the extent to which these results are representative of natural populations, and of the response over more than a few hundred generations is unclear. Here we describe and apply a novel rationale for size-normalizing the mass of the calcite plates produced by the most abundant family of coccolithophores, the Noëlaerhabdaceae. On average, ancient populations subjected to coupled gradual increases in [CO 2 (aq)] and temperature over a few million generations in a natural environment become relatively more highly calcified, implying a positive climatic feedback. We hypothesize that this is the result of selection manifest in natural populations over millennial timescales, so has necessarily eluded laboratory experiments.

Adult exposure to ocean acidification is maladaptive for larvae of the Sydney rock oyster Saccostrea glomerata in the presence of multiple stressors.

PubMed

Parker, Laura M; O'Connor, Wayne A; Byrne, Maria; Coleman, Ross A; Virtue, Patti; Dove, Michael; Gibbs, Mitchell; Spohr, Lorraine; Scanes, Elliot; Ross, Pauline M

2017-02-01

Parental effects passed from adults to their offspring have been identified as a source of rapid acclimation that may allow marine populations to persist as our surface oceans continue to decrease in pH. Little is known, however, whether parental effects are beneficial for offspring in the presence of multiple stressors. We exposed adults of the oyster Saccostrea glomerata to elevated CO 2 and examined the impacts of elevated CO 2 (control = 392; 856 µatm) combined with elevated temperature (control = 24; 28°C), reduced salinity (control = 35; 25) and reduced food concentration (control = full; half diet) on their larvae. Adult exposure to elevated CO 2 had a positive impact on larvae reared at elevated CO 2 as a sole stressor, which were 8% larger and developed faster at elevated CO 2 compared with larvae from adults exposed to ambient CO 2 These larvae, however, had significantly reduced survival in all multistressor treatments. This was particularly evident for larvae reared at elevated CO 2 combined with elevated temperature or reduced food concentration, with no larvae surviving in some treatment combinations. Larvae from CO 2 -exposed adults had a higher standard metabolic rate. Our results provide evidence that parental exposure to ocean acidification may be maladaptive when larvae experience multiple stressors. © 2017 The Author(s).

Adult exposure to ocean acidification is maladaptive for larvae of the Sydney rock oyster Saccostrea glomerata in the presence of multiple stressors

PubMed Central

O'Connor, Wayne A.; Byrne, Maria; Virtue, Patti; Dove, Michael; Gibbs, Mitchell; Spohr, Lorraine; Scanes, Elliot; Ross, Pauline M.

2017-01-01

Parental effects passed from adults to their offspring have been identified as a source of rapid acclimation that may allow marine populations to persist as our surface oceans continue to decrease in pH. Little is known, however, whether parental effects are beneficial for offspring in the presence of multiple stressors. We exposed adults of the oyster Saccostrea glomerata to elevated CO2 and examined the impacts of elevated CO2 (control = 392; 856 µatm) combined with elevated temperature (control = 24; 28°C), reduced salinity (control = 35; 25) and reduced food concentration (control = full; half diet) on their larvae. Adult exposure to elevated CO2 had a positive impact on larvae reared at elevated CO2 as a sole stressor, which were 8% larger and developed faster at elevated CO2 compared with larvae from adults exposed to ambient CO2. These larvae, however, had significantly reduced survival in all multistressor treatments. This was particularly evident for larvae reared at elevated CO2 combined with elevated temperature or reduced food concentration, with no larvae surviving in some treatment combinations. Larvae from CO2-exposed adults had a higher standard metabolic rate. Our results provide evidence that parental exposure to ocean acidification may be maladaptive when larvae experience multiple stressors. PMID:28202683

Surface radiation fluxes in transient climate simulations

NASA Astrophysics Data System (ADS)

Garratt, J. R.; O'Brien, D. M.; Dix, M. R.; Murphy, J. M.; Stephens, G. L.; Wild, M.

1999-01-01

Transient CO 2 experiments from five coupled climate models, in which the CO 2 concentration increases at rates of 0.6-1.1% per annum for periods of 75-200 years, are used to document the responses of surface radiation fluxes, and associated atmospheric properties, to the CO 2 increase. In all five models, the responses of global surface temperature and column water vapour are non-linear and fairly tightly constrained. Thus, global warming lies between 1.9 and 2.7 K at doubled, and between 3.1 and 4.1 K at tripled, CO 2, whilst column water vapour increases by between 3.5 and 4.5 mm at doubled, and between 7 and 8 mm at tripled, CO 2. Global cloud fraction tends to decrease by 1-2% out to tripled CO 2, mainly the result of decreases in low cloud. Global increases in column water, and differences in these increases between models, are mainly determined by the warming of the tropical oceans relative to the middle and high latitudes; these links are emphasised in the zonal profiles of warming and column water vapour increase, with strong water vapour maxima in the tropics. In all models the all-sky shortwave flux to the surface S↓ (global, annual average) changes by less than 5 W m -2 out to tripled CO 2, in some cases being essentially invariant in time. In contrast, the longwave flux to the surface L↓ increases significantly, by 25 W m -2 typically at tripled CO 2. The variations of S↓ and L↓ (clear-sky and all-sky fluxes) with increase in CO 2 concentration are generally non-linear, reflecting the effects of ocean thermal inertia, but as functions of global warming are close to linear in all five models. This is best illustrated for the clear-sky downwelling fluxes, and the net radiation. Regionally, as illustrated in zonal profiles and global distributions, greatest changes in both S↓ and L↓ are the result primarily of local maxima in warming and column water vapour increases.

Ocean acidification impacts bacteria-phytoplankton coupling at low-nutrient conditions

NASA Astrophysics Data System (ADS)

Hornick, Thomas; Bach, Lennart T.; Crawfurd, Katharine J.; Spilling, Kristian; Achterberg, Eric P.; Woodhouse, Jason N.; Schulz, Kai G.; Brussaard, Corina P. D.; Riebesell, Ulf; Grossart, Hans-Peter

2017-01-01

The oceans absorb about a quarter of the annually produced anthropogenic atmospheric carbon dioxide (CO2), resulting in a decrease in surface water pH, a process termed ocean acidification (OA). Surprisingly little is known about how OA affects the physiology of heterotrophic bacteria or the coupling of heterotrophic bacteria to phytoplankton when nutrients are limited. Previous experiments were, for the most part, undertaken during productive phases or following nutrient additions designed to stimulate algal blooms. Therefore, we performed an in situ large-volume mesocosm ( ˜ 55 m3) experiment in the Baltic Sea by simulating different fugacities of CO2 (fCO2) extending from present to future conditions. The study was conducted in July-August after the nominal spring bloom, in order to maintain low-nutrient conditions throughout the experiment. This resulted in phytoplankton communities dominated by small-sized functional groups (picophytoplankton). There was no consistent fCO2-induced effect on bacterial protein production (BPP), cell-specific BPP (csBPP) or biovolumes (BVs) of either free-living (FL) or particle-associated (PA) heterotrophic bacteria, when considered as individual components (univariate analyses). Permutational Multivariate Analysis of Variance (PERMANOVA) revealed a significant effect of the fCO2 treatment on entire assemblages of dissolved and particulate nutrients, metabolic parameters and the bacteria-phytoplankton community. However, distance-based linear modelling only identified fCO2 as a factor explaining the variability observed amongst the microbial community composition, but not for explaining variability within the metabolic parameters. This suggests that fCO2 impacts on microbial metabolic parameters occurred indirectly through varying physicochemical parameters and microbial species composition. Cluster analyses examining the co-occurrence of different functional groups of bacteria and phytoplankton further revealed a separation of the four fCO2-treated mesocosms from both control mesocosms, indicating that complex trophic interactions might be altered in a future acidified ocean. Possible consequences for nutrient cycling and carbon export are still largely unknown, in particular in a nutrient-limited ocean.

Three dimensional global modeling of atmospheric CO2

NASA Technical Reports Server (NTRS)

Fung, I.; Hansen, J.; Rind, D.

1983-01-01

A model was developed to study the prospects of extracting information on carbon dioxide sources and sinks from observed CO2 variations. The approach uses a three dimensional global transport model, based on winds from a 3-D general circulation model (GCM), to advect CO2 noninteractively, i.e., as a tracer, with specified sources and sinks of CO2 at the surface. The 3-D model employed is identified and biosphere, ocean and fossil fuel sources and sinks are discussed. Some preliminary model results are presented.

Re-evaluating the 1940s CO2 plateau

NASA Astrophysics Data System (ADS)

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

2016-09-01

The high-resolution CO2 record from Law Dome ice core reveals that atmospheric CO2 concentration stalled during the 1940s (so-called CO2 plateau). Since the fossil-fuel emissions did not decrease during the period, this stalling implies the persistence of a strong sink, perhaps sustained for as long as a decade or more. Double-deconvolution analyses have attributed this sink to the ocean, conceivably as a response to the very strong El Niño event in 1940-1942. However, this explanation is questionable, as recent ocean CO2 data indicate that the range of variability in the ocean sink has been rather modest in recent decades, and El Niño events have generally led to higher growth rates of atmospheric CO2 due to the offsetting terrestrial response. Here, we use the most up-to-date information on the different terms of the carbon budget: fossil-fuel emissions, four estimates of land-use change (LUC) emissions, ocean uptake from two different reconstructions, and the terrestrial sink modelled by the TRENDY project to identify the most likely causes of the 1940s plateau. We find that they greatly overestimate atmospheric CO2 growth rate during the plateau period, as well as in the 1960s, in spite of giving a plausible explanation for most of the 20th century carbon budget, especially from 1970 onwards. The mismatch between reconstructions and observations during the CO2 plateau epoch of 1940-1950 ranges between 0.9 and 2.0 Pg C yr-1, depending on the LUC dataset considered. This mismatch may be explained by (i) decadal variability in the ocean carbon sink not accounted for in the reconstructions we used, (ii) a further terrestrial sink currently missing in the estimates by land-surface models, or (iii) LUC processes not included in the current datasets. Ocean carbon models from CMIP5 indicate that natural variability in the ocean carbon sink could explain an additional 0.5 Pg C yr-1 uptake, but it is unlikely to be higher. The impact of the 1940-1942 El Niño on the observed stabilization of atmospheric CO2 cannot be confirmed nor discarded, as TRENDY models do not reproduce the expected concurrent strong decrease in terrestrial uptake. Nevertheless, this would further increase the mismatch between observed and modelled CO2 growth rate during the CO2 plateau epoch. Tests performed using the OSCAR (v2.2) model indicate that changes in land use not correctly accounted for during the period (coinciding with drastic socioeconomic changes during the Second World War) could contribute to the additional sink required. Thus, the previously proposed ocean hypothesis for the 1940s plateau cannot be confirmed by independent data. Further efforts are required to reduce uncertainty in the different terms of the carbon budget during the first half of the 20th century and to better understand the long-term variability of the ocean and terrestrial CO2 sinks.

Enhanced Weathering Strategies for Stabilizing Climate and Averting Ocean Acidification

NASA Technical Reports Server (NTRS)

Taylor, Lyla L.; Quirk, Joe; Thorley, Rachel M. S.; Kharecha, Pushker A.; Hansen, James; Ridgwell, Andy; Lomas, Mark R.; Banwart, Steve A.; Beerling, David J.

2015-01-01

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30-300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m(exp -2) yr (exp -1)) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions.

Enhanced weathering strategies for stabilizing climate and averting ocean acidification

NASA Astrophysics Data System (ADS)

Taylor, Lyla L.; Quirk, Joe; Thorley, Rachel M. S.; Kharecha, Pushker A.; Hansen, James; Ridgwell, Andy; Lomas, Mark R.; Banwart, Steve A.; Beerling, David J.

2016-04-01

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30-300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m-2 yr-1) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions.

Enhanced Weathering Strategies for Stabilizing Climate and Averting Ocean Acidification - Supplementary Information

NASA Technical Reports Server (NTRS)

Taylor, Lyla L.; Quirk, Joe; Thorley, Rachel M. S.; Kharecha, Pushker A.; Hansen, James; Ridgwell, Andy; Lomas, Mark R.; Banwart, Steve A.; Beerling, David J.

2015-01-01

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30-300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m(exp. -2) yr (exp -1)) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions.

Changes in anthropogenic carbon storage in the Northeast Pacific in the last decade

NASA Astrophysics Data System (ADS)

Chu, Sophie N.; Wang, Zhaohui Aleck; Doney, Scott C.; Lawson, Gareth L.; Hoering, Katherine A.

2016-07-01

In order to understand the ocean's role as a sink for anthropogenic carbon dioxide (CO2), it is important to quantify changes in the amount of anthropogenic CO2 stored in the ocean interior over time. From August to September 2012, an ocean acidification cruise was conducted along a portion of the P17N transect (50°N 150°W to 33.5°N 135°W) in the Northeast Pacific. These measurements are compared with data from the previous occupation of this transect in 2001 to estimate the change in the anthropogenic CO2 inventory in the Northeast Pacific using an extended multiple linear regression (eMLR) approach. Maximum increases in the surface waters were 11 µmol kg-1 over 11 years near 50°N. Here, the penetration depth of anthropogenic CO2 only reached ˜300 m depth, whereas at 33.5°N, penetration depth reached ˜600 m. The average increase of the depth-integrated anthropogenic carbon inventory was 0.41 ± 0.12 mol m-2 yr-1 across the transect. Lower values down to 0.20 mol m-2 yr-1 were observed in the northern part of the transect near 50°N and increased up to 0.55 mol m-2 yr-1 toward 33.5°N. This increase in anthropogenic carbon in the upper ocean resulted in an average pH decrease of 0.002 ± 0.0003 pH units yr-1 and a 1.8 ± 0.4 m yr-1 shoaling rate of the aragonite saturation horizon. An average increase in apparent oxygen utilization of 13.4 ± 15.5 µmol kg-1 centered on isopycnal surface 26.6 kg m-3 from 2001 to 2012 was also observed.

Spatial variability of upper ocean POC export in the Bay of Bengal and the Indian Ocean determined using particle-reactive 234Th

NASA Astrophysics Data System (ADS)

Subha Anand, S.; Rengarajan, R.; Sarma, V. V. S. S.; Sudheer, A. K.; Bhushan, R.; Singh, S. K.

2017-05-01

The northern Indian Ocean is globally significant for its seasonally reversing winds, upwelled nutrients, high biological production, and expanding oxygen minimum zones. The region acts as sink and source for atmospheric CO2. However, the efficiency of the biological carbon pump to sequester atmospheric CO2 and export particulate organic carbon from the surface is not well known. To quantify the upper ocean carbon export flux and to estimate the efficiency of biological carbon pump in the Bay of Bengal and the Indian Ocean, seawater profiles of total 234Th were measured from surface to 300 m depth at 13 stations from 19.9°N to 25.3°S in a transect along 87°E, during spring intermonsoon period (March-April 2014). Results showed enhanced in situ primary production in the equatorial Indian Ocean and the central Bay of Bengal and varied from 13.2 to 173.8 mmol C m-2 d-1. POC export flux in this region varied from 0 to 7.7 mmol C m-2 d-1. Though high carbon export flux was found in the equatorial region, remineralization of organic carbon in the surface and subsurface waters considerably reduced organic carbon export in the Bay of Bengal. Annually recurring anticyclonic eddies enhanced organic carbon utilization and heterotrophy. Oxygen minimum zone developed due to stratification and poor ventilation was intensified by subsurface remineralization. 234Th-based carbon export fluxes were not comparable with empirical statistical model estimates based on primary production and temperature. Region-specific refinement of model parameters is required to accurately predict POC export fluxes.

Estimating temporal and spatial variation of ocean surface pCO2 in the North Pacific using a self-organizing map neural network technique

NASA Astrophysics Data System (ADS)

Nakaoka, S.; Telszewski, M.; Nojiri, Y.; Yasunaka, S.; Miyazaki, C.; Mukai, H.; Usui, N.

2013-09-01

This study uses a neural network technique to produce maps of the partial pressure of oceanic carbon dioxide (pCO2sea) in the North Pacific on a 0.25° latitude × 0.25° longitude grid from 2002 to 2008. The pCO2sea distribution was computed using a self-organizing map (SOM) originally utilized to map the pCO2sea in the North Atlantic. Four proxy parameters - sea surface temperature (SST), mixed layer depth, chlorophyll a concentration, and sea surface salinity (SSS) - are used during the training phase to enable the network to resolve the nonlinear relationships between the pCO2sea distribution and biogeochemistry of the basin. The observed pCO2sea data were obtained from an extensive dataset generated by the volunteer observation ship program operated by the National Institute for Environmental Studies (NIES). The reconstructed pCO2sea values agreed well with the pCO2sea measurements, with the root-mean-square error ranging from 17.6 μatm (for the NIES dataset used in the SOM) to 20.2 μatm (for independent dataset). We confirmed that the pCO2sea estimates could be improved by including SSS as one of the training parameters and by taking into account secular increases of pCO2sea that have tracked increases in atmospheric CO2. Estimated pCO2sea values accurately reproduced pCO2sea data at several time series locations in the North Pacific. The distributions of pCO2sea revealed by 7 yr averaged monthly pCO2sea maps were similar to Lamont-Doherty Earth Observatory pCO2sea climatology, allowing, however, for a more detailed analysis of biogeochemical conditions. The distributions of pCO2sea anomalies over the North Pacific during the winter clearly showed regional contrasts between El Niño and La Niña years related to changes of SST and vertical mixing.

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

NASA Astrophysics Data System (ADS)

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

2015-06-01

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

Seasonality of biological and physical controls on surface ocean CO2 from hourly observations at the Southern Ocean Time Series site south of Australia.

NASA Astrophysics Data System (ADS)

Shadwick, E. H.; Trull, T. W.; Tilbrook, B. D.; Sutton, A.; Sabine, C. L.

2016-02-01

The Subantarctic Zone (SAZ), which covers the northern half of the Southern Ocean between the Subtropical and Subantarctic Fronts is important for air-sea CO2 exchange, ventilation of the lower thermocline, and nutrient supply for global ocean productivity. The first high-resolution autonomous observations of mixed layer CO2 partial pressure (pCO2) and hydrographic properties in the SAZ covering a full annual cycle will be presented. The annual cycle of pCO2 is decomposed into physical and biological drivers: after the summer biological pCO2 depletion (driven by an annual net community production of 2.45±1.47 mol C m-2 yr-1), the return to near atmospheric equilibrium proceeds slowly, driven by entrainment in early autumn when mixed layers deepen from <100 to 200m, but only achieving full equilibration in late winter/early spring as respiration completes the annual cycle. The shutdown of winter convection and associated mixed layer shoaling proceeds intermittently, appearing to frustrate the initiation of production. Horizontal processes, identified from salinity anomalies, are associated with biological pCO2 signatures, but with differing impacts in winter (when they reflect far-field variations in dissolved inorganic carbon and/or biomass) and summer (when they suggest promotion of local production by the relief of silicic acid or iron limitation). These results provide clarity on SAZ seasonal carbon cycling and demonstrate that the magnitude of the annual pCO2 cycle is twice as large as that in the subarctic high-nutrient, low-chlorophyll waters, which can inform the selection of optimal global models in this region.

Enhanced weathering strategies for cooling the planet and saving coral reefs

NASA Astrophysics Data System (ADS)

Beerling, D. J.; Taylor, L.; Quirk, J.; Thorley, R.; Kharecha, P. A.; Hansen, J. E.; Ridgwell, A. J.; Lomas, M.; Banwart, S. A.

2014-12-01

Acceleration of the chemical weathering sink for atmospheric CO2 via distribution of pulverized silicate rocks across terrestrial landscapes has been proposed as a macro-engineering Carbon Dioxide Removal (CDR) scheme, but its effectiveness and response to ongoing global change is poorly understood. We employ a detailed spatially resolved weathering model driven by two ensemble Representative Concentration Pathway (RCP) projections of 21st Century climate (RCP8.5 and RCP4.5) to assess enhanced weathering and examine feedbacks on atmospheric CO2 and ocean carbonate biogeochemistry. Atmospheric CO2 reduction of ~100-260 ppm by year 2100, the range depending mainly on rock composition, is obtained by spreading 5 kg m-2 yr-1 over 20 Mkm2 tropical weathering 'hotspots'. Ocean acidification is neutralized in RCP4.5 and ameliorated in RCP8.5 due to enhanced land-ocean export of weathered alkalinity products and reduced CO2 forcings, and the aragonite saturation state of surface oceans is raised to >3.5, thus avoiding likely extinction of coral reef ecosystems. We suggest that accelerated weathering has substantial potential to help limit global warming and benefits to marine life not obtained from other CDR approaches, but major issues of cost, social acceptability, and potential unanticipated consequences should encourage urgent efforts to phase down fossil fuel emissions.

Influence of elevated CO2 concentrations on cell division and nitrogen fixation rates in the bloom-forming cyanobacterium Nodularia spumigena

NASA Astrophysics Data System (ADS)

Czerny, J.; Ramos, J. Barcelos E.; Riebesell, U.

2009-04-01

The surface ocean currently absorbs about one-fourth of the CO2 emitted to the atmosphere from human activities. As this CO2 dissolves in seawater, it reacts with seawater to form carbonic acid, increasing ocean acidity and shifting the partitioning of inorganic carbon species towards increased CO2 at the expense of CO32- concentrations. While the decrease in [CO32-] and/or increase in [H+] has been found to adversely affect many calcifying organisms, some photosynthetic organisms appear to benefit from increasing [CO2]. Among these is the cyanobacterium Trichodesmium, a predominant diazotroph (nitrogen-fixing) in large parts of the oligotrophic oceans, which responded with increased carbon and nitrogen fixation at elevated pCO2. With the mechanism underlying this CO2 stimulation still unknown, the question arises whether this is a common response of diazotrophic cyanobacteria. In this study we therefore investigate the physiological response of Nodularia spumigena, a heterocystous bloom-forming diazotroph of the Baltic Sea, to CO2-induced changes in seawater carbonate chemistry. N. spumigena reacted to seawater acidification/carbonation with reduced cell division rates and nitrogen fixation rates, accompanied by significant changes in carbon and phosphorus quota and elemental composition of the formed biomass. Possible explanations for the contrasting physiological responses of Nodularia compared to Trichodesmium may be found in the different ecological strategies of non-heterocystous (Trichodesmium) and heterocystous (Nodularia) cyanobacteria.

DOE Office of Scientific and Technical Information (OSTI.GOV)

PAUL, JOHN H

Oceanic river plumes represent some of the most productive environments on Earth. As major conduits for freshwater and nutrients into the coastal ocean, their impact on water column ecosystems extend for up to a thousand km into oligotrophic oceans. Upon entry into the oceans rivers are tremendous sources of CO2 and dissolved inorganic carbon (DIC). Yet owing to increased light transmissivity from sediment deposition coupled with the influx of nutrients, dramatic CO2 drawdown occurs, and plumes rapidly become sinks for CO2. Using state-of-the-art gene expression technology, we have examined the molecular biodiversity of CO2 fixation in the Mississippi River Plumemore » (MRP; two research cruises) and the Orinoco River Plume (ORP; one cruise). When the MRP extends far into the Gulf because of entrainment with the Loop Current, MRP production (carbon fixation) can account for up to 41% of the surface production in the Gulf of Mexico. Nearer-shore plume stations (“high plume,” salinity< 32 ppt) had tremendous CO2 drawdown that was correlated to heterokont (principally diatom) carbon fixation gene expression. The principal form of nitrogen for this production based upon 15N studies was urea, believed to be from anthropogenic origin (fertilizer) from the MRP watershed. Intermediate plume environments (salinity 34 ppt) were characterized by high levels of Synechococcuus carbon fixation that was fueled by regenerated ammonium. Non-plume stations were characterized by high light Prochlorococcus carbon fixation gene expression that was positively correlated with dissolved CO2 concentrations. Although data from the ORP cruise is still being analyzed, some similarities and striking differences were found between the ORP and MRP. High levels of heterokont carbon fixation gene expression that correlated with CO2 drawdown were observed in the high plume, yet the magnitude of this phenomenon was far below that of the MRP, most likely due to the lower levels of anthropogenic nutrient input. The offshore ORP was characterized by haptophyte and in places Prochlorococcus carbon fixation gene expression in surface water, with greater heterokont rbcL RNA at SCM depths. MODIS satellite chlorophyll-a data implied a plume of high chlorophyll water far into the eastern Caribbean, yet field observations did not support this, most likely because of high levels of colored dissolved organic matter (cDOM) in the ORP. The presence of pelagic nitrogen fixers (Trichodesmium and cyanobacterial diatom endosymbionts) most likely provided N for the offshore MRP production. The results underscore the importance of oceanic river plumes as sinks for CO2 and the need for their incorporation in global carbon models as well as estimates of CO2 sequestration.« less

Instability and breakdown of the coral-algae symbiosis upon exceedence of the interglacial pCO2 threshold (>260 ppmv): the "missing" Earth-System feedback mechanism

NASA Astrophysics Data System (ADS)

Wooldridge, Scott A.

2017-12-01

Changes in the atmospheric partial pressure of CO2 ( pCO2) leads to predictable impacts on the surface ocean carbonate system. Here, the importance of atmospheric pCO2 <260 ppmv is established for the optimum performance (and stability) of the algal endosymbiosis employed by a key suite of tropical reef-building coral species. Violation of this symbiotic threshold is revealed as a prerequisite for major historical reef extinction events, glacial-interglacial feedback climate cycles, and the modern decline of coral reef ecosystems. Indeed, it is concluded that this symbiotic threshold enacts a fundamental feedback mechanism needed to explain the characteristic dynamics (and drivers) of the coupled land-ocean-atmosphere carbon cycle of the Earth System since the mid-Miocene, some 25 million yr ago.

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

USGS Publications Warehouse

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

2013-01-01

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

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

USGS Publications Warehouse

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

2013-01-01

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

Enhanced transfer of organic matter to higher trophic levels caused by ocean acidification and its implications for export production: A mass balance approach.

PubMed

Boxhammer, Tim; Taucher, Jan; Bach, Lennart T; Achterberg, Eric P; Algueró-Muñiz, María; Bellworthy, Jessica; Czerny, Jan; Esposito, Mario; Haunost, Mathias; Hellemann, Dana; Ludwig, Andrea; Yong, Jaw C; Zark, Maren; Riebesell, Ulf; Anderson, Leif G

2018-01-01

Ongoing acidification of the ocean through uptake of anthropogenic CO2 is known to affect marine biota and ecosystems with largely unknown consequences for marine food webs. Changes in food web structure have the potential to alter trophic transfer, partitioning, and biogeochemical cycling of elements in the ocean. Here we investigated the impact of realistic end-of-the-century CO2 concentrations on the development and partitioning of the carbon, nitrogen, phosphorus, and silica pools in a coastal pelagic ecosystem (Gullmar Fjord, Sweden). We covered the entire winter-to-summer plankton succession (100 days) in two sets of five pelagic mesocosms, with one set being CO2 enriched (~760 μatm pCO2) and the other one left at ambient CO2 concentrations. Elemental mass balances were calculated and we highlight important challenges and uncertainties we have faced in the closed mesocosm system. Our key observations under high CO2 were: (1) A significantly amplified transfer of carbon, nitrogen, and phosphorus from primary producers to higher trophic levels, during times of regenerated primary production. (2) A prolonged retention of all three elements in the pelagic food web that significantly reduced nitrogen and phosphorus sedimentation by about 11 and 9%, respectively. (3) A positive trend in carbon fixation (relative to nitrogen) that appeared in the particulate matter pool as well as the downward particle flux. This excess carbon counteracted a potential reduction in carbon sedimentation that could have been expected from patterns of nitrogen and phosphorus fluxes. Our findings highlight the potential for ocean acidification to alter partitioning and cycling of carbon and nutrients in the surface ocean but also show that impacts are temporarily variable and likely depending upon the structure of the plankton food web.

Global Biogeochemical Fluxes Program for the Ocean Observatories Initiative: A Proposal. (Invited)

NASA Astrophysics Data System (ADS)

Ulmer, K. M.; Taylor, C.

2010-12-01

The overarching emphasis of the Global Biogeochemical Flux Ocean Observatories Initiative is to assess the role of oceanic carbon, both living and non-, in the Earth climate system. Modulation of atmospheric CO2 and its influence on global climate is a function of the quantitative capacity of the oceans to sequester organic carbon into deep waters. Critical to our understanding of the role of the oceans in the global cycling of carbon are the quantitative dynamics in both time and space of the fixation of CO2 into organic matter by surface ocean primary production and removal of this carbon to deep waters via the “biological pump”. To take the next major step forward in advancing our understanding of the oceanic biological pump, a global observation program is required that: (i) greatly improves constraints on estimates of global marine primary production (PP), a critical factor in understanding the global CO2 cycle and for developing accurate estimates of export production (EP); (ii) explores the spatiotemporal links between PP, EP and the biogeochemical processes that attenuate particulate organic carbon (POC) flux; (iii) characterizes microbial community structure and dynamics both in the surface and deep ocean; (iv) develops a comprehensive picture of the chemical and biological processes that take place from the surface ocean to the sea floor; (v) provides unique time-series samples for detailed laboratory-based chemical and biological characterization and tracer studies that will enable connections to be made between the operation of the biological pump at present and in the geologic past. The primary goal is to provide high quality biological and biogeochemical observational data for the modeling and prediction efforts of the global CO2 cycle research community. Crucial to the realization of the GBF-OOI is the development of reliable, long-term, time-series ocean observation platforms capable of precise and controlled placement of sophisticated biogeochemical sensors/samplers, and in situ experimental systems at a wide range of depths, including close proximity to the sea surface. Significant opportunities exist to exploit sensor miniaturization in combination with recent exponential improvements in “omics” technologies for measurement of nucleic acids, proteins and metabolites with unprecedented throughput and resolution. We will discuss the goals, philosophy, principal experimental and technical approaches and operational challenges. We will outline proposed mooring systems as well as means for accurate, spatiotemporal assessment of: (i) primary production, (ii) constraint of POC export flux with season and depth, (iii) assessment of microbial and zooplankton community structure/function throughout the water column, and (iv) collection and preservation of particulate and water samples for land-based examination of temporal and vertical variability of specific tracers, isotopes, nutrients, DOC and related substances for even more precise measurements of environmental biogeochemical properties. The GBF-OOI will become our Hubble for the sea.

Gases in Seawater

NASA Astrophysics Data System (ADS)

Nightingale, P. D.; Liss, P. S.

2003-12-01

The annual gross and net primary productivity of the surface oceans is similar in size to that on land (IPCC, 2001). Marine productivity drives the cycling of gases such as oxygen (O2), dimethyl sulfide (DMS), carbon monoxide (CO), carbon dioxide (CO2), and methyl iodide (CH3I) which are of fundamental importance in studies of marine productivity, biogeochemical cycles, atmospheric chemistry, climate, and human health, respectively. For example, ˜30% of the world's population (1,570 million) is thought to be at risk of iodine-deficiency disorders that impair mental development (WHO, 1996). The main source of iodine to land is the supply of volatile iodine compounds produced in the ocean and then transferred to the atmosphere via the air-surface interface. The flux of these marine iodine species to the atmosphere is also thought to be important in the oxidation capacity of the troposphere by the production of the iodine oxide radical ( Alicke et al., 1999). A further example is that the net flux of CO2 from the atmosphere to the ocean, ˜1.7±0.5 Gt C yr-1, represents ˜30% of the annual release of anthropogenic CO2 to the atmosphere (IPCC, 2001). This net flux is superimposed on a huge annual flux (90 Gt C yr-1) of CO2 that is cycled "naturally" between the ocean and the atmosphere. The long-term sink for anthropogenic CO2 is recognized as transfer to the ocean from the atmosphere. A final example is the emission of volatile sulfur, in the form of DMS, from the oceans. Not only is an oceanic flux from the oceans needed to balance the loss of sulfur (a bioessential element) from the land via weathering, it has also been proposed as having a major control on climate due to the formation of cloud condensation nuclei (Charlson et al., 1987). Indeed, the existence of DMS and CH3I has been used as evidence in support of the Gaia hypothesis (Lovelock, 1979).There are at least four main processes that affect the concentration of gases in the water column: biological production and consumption, photochemistry, air-sea exchange, and vertical mixing. We will not discuss the effect of vertical mixing on gases in seawater and instead refer the reader to Chapter 6.08. Nor will we consider the deeper oceans as this region is discussed in chapters on benthic fluxes and early diagenesis (Chapter 6.11), the biological pump (Chapter 6.04), and the oceanic calcium carbonate cycle (Chapter 6.19) all in this volume. We will discuss the cycling of gases in surface oceans, including the thermocline, and in particular concentrate on the exchange of various volatile compounds across the air-sea interface.As we will show, while much is known about the cycling of gases such as CO2 and DMS in the water column, frustratingly little is known about many of the chemical species for which the ocean is believed to be a significant source to the atmosphere. We suspect the passage of time will reveal that the cycling of volatile compounds containing selenium and iodine may well prove as complex as that of DMS. Early studies of DMS assumed that it was produced from a precursor compound, dimethylsulfoniopropionate (DMSP), known to be present in some species of phytoplankton, and that the main sink in the water column was exchange across the air-sea interface. We now know that DMSP and DMS are both rapidly cycled in water column by a complex interaction between phytoplankton, microzooplankton, bacteria, and viruses (see Figure 1). Some detailed process experiments have revealed that only ˜10% of the total DMS produced (and less than 1.3% of the DMSP produced) is transferred to the atmosphere, with the bulk of the DMS and DMSP, either being recycled in the water column or photo-oxidized (Archer et al., 2002b).

Ocean acidification stimulates particulate organic carbon accumulation in two Antarctic diatom species under moderate and high natural solar radiation.

PubMed

Heiden, Jasmin P; Thoms, Silke; Bischof, Kai; Trimborn, Scarlett

2018-05-23

Impacts of rising atmospheric CO 2 concentrations and increased daily irradiances from enhanced surface water stratification on phytoplankton physiology in the coastal Southern Ocean remain still unclear. Therefore, in the two Antarctic diatoms Fragilariopsis curta and Odontella weissflogii the effects of moderate and high natural solar radiation combined with either ambient or future pCO 2 on cellular particulate organic carbon (POC) contents and photophysiology were investigated. Results showed that increasing CO 2 concentrations had greater impacts on diatom physiology than exposure to increasing solar radiation. Irrespective of the applied solar radiation regime, cellular POC quotas increased with future pCO 2 in both diatoms. Lowered maximum quantum yields of photochemistry in PSII (F v /F m ) indicated a higher photosensitivity under these conditions, being counteracted by increased cellular concentrations of functional photosynthetic reaction centers. Overall, our results suggest that both bloom-forming Antarctic coastal diatoms might increase carbon contents under future pCO 2 conditions despite reduced physiological fitness. This indicates a higher potential for primary productivity by the two diatom species with important implications for the CO 2 sequestration potential of diatom communities in the future coastal Southern Ocean. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.

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

NASA Astrophysics Data System (ADS)

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

2018-05-01

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

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Volcanic carbon dioxide vents show ecosystem effects of ocean acidification.

PubMed

Hall-Spencer, Jason M; Rodolfo-Metalpa, Riccardo; Martin, Sophie; Ransome, Emma; Fine, Maoz; Turner, Suzanne M; Rowley, Sonia J; Tedesco, Dario; Buia, Maria-Cristina

2008-07-03

The atmospheric partial pressure of carbon dioxide (p(CO(2))) will almost certainly be double that of pre-industrial levels by 2100 and will be considerably higher than at any time during the past few million years. The oceans are a principal sink for anthropogenic CO(2) where it is estimated to have caused a 30% increase in the concentration of H(+) in ocean surface waters since the early 1900s and may lead to a drop in seawater pH of up to 0.5 units by 2100 (refs 2, 3). Our understanding of how increased ocean acidity may affect marine ecosystems is at present very limited as almost all studies have been in vitro, short-term, rapid perturbation experiments on isolated elements of the ecosystem. Here we show the effects of acidification on benthic ecosystems at shallow coastal sites where volcanic CO(2) vents lower the pH of the water column. Along gradients of normal pH (8.1-8.2) to lowered pH (mean 7.8-7.9, minimum 7.4-7.5), typical rocky shore communities with abundant calcareous organisms shifted to communities lacking scleractinian corals with significant reductions in sea urchin and coralline algal abundance. To our knowledge, this is the first ecosystem-scale validation of predictions that these important groups of organisms are susceptible to elevated amounts of p(CO(2)). Sea-grass production was highest in an area at mean pH 7.6 (1,827 (mu)atm p(CO(2))) where coralline algal biomass was significantly reduced and gastropod shells were dissolving due to periods of carbonate sub-saturation. The species populating the vent sites comprise a suite of organisms that are resilient to naturally high concentrations of p(CO(2)) and indicate that ocean acidification may benefit highly invasive non-native algal species. Our results provide the first in situ insights into how shallow water marine communities might change when susceptible organisms are removed owing to ocean acidification.

Exploring diurnal and seasonal characteristics of global carbon cycle with GISS Model E2 GCM

NASA Astrophysics Data System (ADS)

Aleinov, I. D.; Kiang, N. Y.; Romanou, A.

2017-12-01

The ability to properly model surface carbon fluxes on the diurnal and seasonal time scale is a necessary requirement for understanding of the global carbon cycle. It is also one of the most challenging tasks faced by modern General Circulation Models (GCMs) due to complexity of the algorithms and variety of relevant spatial and temporal scales. The observational data, though abundant, is difficult to interpret at the global scale, because flux tower observations are very sparse for large impact areas (such as Amazon and African rainforest and most of Siberia) and satellite missions often struggle to produce sufficiently high confidence data over the land and may be missing CO2 amounts near the surface due to the nature of the method. In this work we use the GISS Model E2 GCM to perform a subset of experiments proposed by the Coupled Climate-Carbon Cycle Model Intercomparison Project (C4MIP) and relate the results to available observations.The GISS Model E2 GCM is currently equipped with a complete global carbon cycle algorithm. Its surface carbon fluxes are computed by the Ent Terrestrial Biosphere Model (Ent TBM) over the land with observed leaf area index of the Moderate Resolution Imaging Spectrometer (MODIS) and by the NASA Ocean Biogeochemistry Model (NOBM) over the ocean. The propagation of atmospheric CO2 is performed by a generic Model E2 tracer algorithm, which is based on a quadratic upstream method (Prather 1986). We perform a series spin-up experiments for preindustrial climate conditions and fixed preindustrial atmospheric CO2 concentration. First, we perform separate spin-up simulations each for terrestrial and ocean carbon. We then combine the spun-up states and perform a coupled spin-up simulation until the model reaches a sufficient equilibrium. We then release restrictions on CO2 concentration and allow it evolve freely, driven only by simulated surface fluxes. We then study the results of the unforced run, comparing the amplitude and the phase of diurnal and seasonal variation of atmospheric CO2 concentration to selected flux tower observations and OCO-2 satellite datasets.

Introduction to this special issue on ocean acidification: the pathway from science to policy

USGS Publications Warehouse

Mathis, Jeremy T.; Cooley, Sarah R.; Yates, Kimberly K.; Williamson, Phillip

2015-01-01

Ocean acidification (OA) is a progressive decrease in the pH of seawater over decades, caused primarily by uptake of excess atmospheric CO2 and accompanied by changes in seawater carbonate chemistry. Scientific studies designed to examine the effects of anthropogenic carbon dioxide (CO2) emissions on global carbon fluxes have also led to the detection of OA. During the last decade, this phenomenon has surged to the attention of not only scientists but also policymakers and the public. OA chemistry is well understood and follows first principles of acid-base chemistry (e.g., Gattuso and Hansson, 2011; Box 1 in McLaughlin et al.). Today, total anthropogenic release of CO2 exceeds nine petagrams of carbon annually, with ~85% coming directly from industrial sources and ~15% from changes in land use. The three major sinks for this CO2 are: ~46% of CO2 emitted remains in the atmosphere, ~29% is absorbed by the terrestrial biosphere, and the ocean absorbs the remaining ~26% (Le Quéré et al., 2014), resulting in OA. Since the Industrial Revolution, global average surface ocean pH has dropped 0.1 unit (about a 30% increase in acidity; IPCC, 2013), and it is expected to drop another 0.3 to 0.4 units by 2100 (100-150% increase in acidity) if CO2 emissions continue in a business-as-usual scenario (Orr et al., 2005; IPCC, 2013). Some areas of the ocean, such as coastal regions, upwelling zones, and polar seas, may be subjected to much greater chemical perturbations from OA than indicated by such globally averaged values (e.g., Feely et al., 2008; Mathis et al.).

Poorly cemented coral reefs of the eastern tropical Pacific: possible insights into reef development in a high-CO2 world.

PubMed

Manzello, Derek P; Kleypas, Joan A; Budd, David A; Eakin, C Mark; Glynn, Peter W; Langdon, Chris

2008-07-29

Ocean acidification describes the progressive, global reduction in seawater pH that is currently underway because of the accelerating oceanic uptake of atmospheric CO(2). Acidification is expected to reduce coral reef calcification and increase reef dissolution. Inorganic cementation in reefs describes the precipitation of CaCO(3) that acts to bind framework components and occlude porosity. Little is known about the effects of ocean acidification on reef cementation and whether changes in cementation rates will affect reef resistance to erosion. Coral reefs of the eastern tropical Pacific (ETP) are poorly developed and subject to rapid bioerosion. Upwelling processes mix cool, subthermocline waters with elevated pCO(2) (the partial pressure of CO(2)) and nutrients into the surface layers throughout the ETP. Concerns about ocean acidification have led to the suggestion that this region of naturally low pH waters may serve as a model of coral reef development in a high-CO(2) world. We analyzed seawater chemistry and reef framework samples from multiple reef sites in the ETP and found that a low carbonate saturation state (Omega) and trace abundances of cement are characteristic of these reefs. These low cement abundances may be a factor in the high bioerosion rates previously reported for ETP reefs, although elevated nutrients in upwelled waters may also be limiting cementation and/or stimulating bioerosion. ETP reefs represent a real-world example of coral reef growth in low-Omega waters that provide insights into how the biological-geological interface of coral reef ecosystems will change in a high-CO(2) world.

Method and apparatus for efficient injection of CO2 in oceans

DOEpatents

West, Olivia R.; Tsouris, Constantinos; Liang, Liyuan

2003-07-29

A liquid CO.sub.2 injection system produces a negatively buoyant consolidated stream of liquid CO.sub.2, CO.sub.2 hydrate, and water that sinks upon release at ocean depths in the range of 700-1500 m. In this approach, seawater at a predetermined ocean depth is mixed with the liquid CO.sub.2 stream before release into the ocean. Because mixing is conducted at depths where pressures and temperatures are suitable for CO.sub.2 hydrate formation, the consolidated stream issuing from the injector is negatively buoyant, and comprises mixed CO.sub.2 -hydrate/CO.sub.2 -liquid/water phases. The "sinking" characteristic of the produced stream will prolong the metastability of CO.sub.2 ocean sequestration by reducing the CO.sub.2 dissolution rate into water. Furthermore, the deeper the CO.sub.2 hydrate stream sinks after injection, the more stable it becomes internally, the deeper it is dissolved, and the more dispersed is the resulting CO.sub.2 plume. These factors increase efficiency, increase the residence time of CO2 in the ocean, and decrease the cost of CO.sub.2 sequestration while reducing deleterious impacts of free CO.sub.2 gas in ocean water.

The response of Antarctic sea ice algae to changes in pH and CO2.

PubMed

McMinn, Andrew; Müller, Marius N; Martin, Andrew; Ryan, Ken G

2014-01-01

Ocean acidification substantially alters ocean carbon chemistry and hence pH but the effects on sea ice formation and the CO2 concentration in the enclosed brine channels are unknown. Microbial communities inhabiting sea ice ecosystems currently contribute 10-50% of the annual primary production of polar seas, supporting overwintering zooplankton species, especially Antarctic krill, and seeding spring phytoplankton blooms. Ocean acidification is occurring in all surface waters but the strongest effects will be experienced in polar ecosystems with significant effects on all trophic levels. Brine algae collected from McMurdo Sound (Antarctica) sea ice was incubated in situ under various carbonate chemistry conditions. The carbon chemistry was manipulated with acid, bicarbonate and bases to produce a pCO2 and pH range from 238 to 6066 µatm and 7.19 to 8.66, respectively. Elevated pCO2 positively affected the growth rate of the brine algal community, dominated by the unique ice dinoflagellate, Polarella glacialis. Growth rates were significantly reduced when pH dropped below 7.6. However, when the pH was held constant and the pCO2 increased, growth rates of the brine algae increased by more than 20% and showed no decline at pCO2 values more than five times current ambient levels. We suggest that projected increases in seawater pCO2, associated with OA, will not adversely impact brine algal communities.

Methane mitigation shows significant benefits towards achieving the 1.5 degree target.

NASA Astrophysics Data System (ADS)

Collins, W.; Webber, C.; Cox, P. M.; Huntingford, C.; Lowe, J. A.; Sitch, S.

2017-12-01

Most analyses of allowable carbon emissions to achieve the 1.5 degree target implicitly assume that the ratio of CO2 to non-CO2 greenhouse gases remains near constant, and that all radiative forcing factors have similar impacts on land and ocean carbon storage. Here we determine how plausible reductions in methane emissions will make the carbon targets more feasible. We account for the latest estimates of the methane radiative effect as well as the indirect effects of methane on ozone. We particularly address the differing effects of methane and CO2 mitigation on the land carbon storage including via reduced concentrations of surface ozone. The methodology uses an intermediate complexity climate model (IMOGEN) coupled to a land surface model (JULES) which represents the details of the terrestrial carbon cycle. The carbon emissions inputs to IMOGEN are varied to find allowable pathways consistent with the Paris 1.5 K or 2.0 K targets. The IMOGEN physical parameters are altered to represent the climate characteristics of 38 CMIP5 models (such as climate sensitivity) to provide bounds on the range of allowable CO2 emissions. We examine the effects of three different methane mitigation options that are broadly consistent with the ranges in the SSP scenarios: little mitigation, cost-optimal mitigation, and maximal mitigation. The land and ocean carbon storage increases with methane mitigation, allowing more flexibility in CO2 emission reduction. This is mostly since CO2 fertilisation is reduced less with high methane mitigation, with a small contribution from reduced plant damage with lower surface ozone levels.

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

PubMed

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

2015-09-18

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

Impact of volcanic eruptions on the marine carbon cycle

NASA Astrophysics Data System (ADS)

Segschneider, Joachim; Ulrike, Niemeier; Martin, Wiesner; Claudia, Timmreck

2010-05-01

The impact of volcanic eruptions on the marine carbon cycle is investigated for the example of the Pinatubo eruption with model simulations of the distribution of the ash cloud and deposition on the ocean surface and the impact of the nutrient addition from ash leachates on the oceanic biological production and hence biological carbon pump. Natural variations of aerosols, especially due to large-magnitude volcanic eruptions, are recognized as a significant climate forcing, altering the Earth's radiation balance and thus tending to cause global temperature changes. While the impact of such events on climate and the terrestrial biosphere is relatively well documented, scientific knowledge of their effects on marine ecosystems and consequent feedbacks to the atmosphere is still very limited. In the deep sea, subaerial eruptive events of global significance are commonly recorded as widespread ash layers, which were often found to be associated with increased abundances of planktic organisms. This has led to the hypothesis that the influx of volcanic ash may provide an external nutrient source for primary production (in particular through iron fertilization) in ocean surface waters. Recent laboratory experiments have demonstrated that pristine volcanic ash indeed releases significant amounts of macronutrients and bioactive trace metals (including phosphate, iron and silica) adsorbed to the surface of the ash particles. The release of these components most likely has its largest impact in ocean regions where their availability is crucial for the growth of oceanic biomass, which are the high-nutrient but low-productivity (low-iron) areas in the Pacific and the Southern Ocean. These in turn are neighbored by most of those subaerially active volcanoes that are capable of ejecting huge amounts of aerosols into the high-velocity stratospheric wind fields. The dispersal and fallout of ash thus has a high potential to induce globally significant, transient net CO2 removal from the upper ocean and hence the atmosphere. Large-magnitude eruptions such as of Mount Pinatubo in 1991 were in fact followed by a slowing-down in the increase of atmospheric CO2 for several years, entailing a weakening of the global warming trend. For Mount Pinatubo it has been argued that the estimated CO2 uptake (1.6 x 1015 g C) could have been caused by rapid iron fertilization of the Southern Ocean with about 6.3 x 1015 g of ash. However, this would approximate the overall amount of the ash generated by the eruption, of which about 80% fell out over the South China Sea (~4.9 x 1015 g). This suggests additional avenues for the removal of CO2, among which the 1991 explosive eruption of Cerro Hudson could have played an important role as more than 2 km3 of the aerosols released by the volcano fell out directly over the Southern Ocean.

On the Response of pH to Inorganic Nutrient Enrichment in Well-Mixed Coastal Marine Waters

EPA Science Inventory

Recent concerns about declining pH in the surface ocean in response to anthropogenic increases of CO2 in the atmosphere have raised the question of how this declining baseline of oceanic pH might interact with the much larger diel and seasonal variations of pH in coastal marine e...

Whole water column distribution and carbon isotopic composition of bulk particulate organic carbon, cholesterol and brassicasterol from the Cape Basin to the northern Weddell Gyre in the Southern Ocean

NASA Astrophysics Data System (ADS)

Cavagna, A.-J.; Dehairs, F.; Woule-Ebongué, V.; Bouillon, S.; Planchon, F.; Delille, B.; Bouloubassi, I.

2012-02-01

The combination of concentrations and δ13C signatures of Particulate Organic Carbon (POC) and sterols provides a powerful approach to study ecological and environmental changes both in the modern and ancient ocean, but its application has so far been restricted to the surface area. We applied this tool to study the biogeochemical changes in the modern ocean water column during the BONUS-GoodHope survey (Feb-Mar 2008) from Cape Basin to the northern part of the Weddell Gyre. Cholesterol and brassicasterol were chosen as ideal biomarkers of the heterotrophic and autotrophic carbon pools, respectively, because of their ubiquitous and relatively refractory nature. We document depth distributions of concentrations (relative to bulk POC) and δ13C signatures of cholesterol and brassicasterol from the Cape Basin to the northern Weddell Gyre combined with CO2 aq. surface concentration variation. While relationships between surface water CO2 aq. and δ13C of bulk POC and biomarkers have been previously established for surface waters, our data show that these remain valid in deeper waters, suggesting that δ13C signatures of certain biomarkers could be developed as proxies for surface water CO2 aq. Our data suggest a key role of zooplankton fecal aggregates in carbon export for this part of the Southern Ocean. We observed a general increase in sterol δ13C signatures with depth, which is likely related to a combination of particle size effects, selective feeding on larger cells by zooplankton, and growth rate related effects Additionally, in the southern part of the transect south of the Polar Front (PF), the release of sea-ice algae is hypothesized to influence the isotopic signature of sterols in the open ocean. Overall, combined use of δ13C and concentrations measurements of both bulk organic C and specific sterol markers throughout the water column shows the promising potential of analyzing δ13C signatures of individual marine sterols to explore the recent history of plankton and the fate of organic matter in the SO.

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

PubMed Central

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

2013-01-01

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

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

NASA Astrophysics Data System (ADS)

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

2018-04-01

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

Reviews and Syntheses: Ocean acidification and its potential impacts on marine ecosystems

NASA Astrophysics Data System (ADS)

Mostofa, Khan M. G.; Liu, Cong-Qiang; Zhai, WeiDong; Minella, Marco; Vione, Davide; Gao, Kunshan; Minakata, Daisuke; Arakaki, Takemitsu; Yoshioka, Takahito; Hayakawa, Kazuhide; Konohira, Eiichi; Tanoue, Eiichiro; Akhand, Anirban; Chanda, Abhra; Wang, Baoli; Sakugawa, Hiroshi

2016-03-01

Ocean acidification, a complex phenomenon that lowers seawater pH, is the net outcome of several contributions. They include the dissolution of increasing atmospheric CO2 that adds up with dissolved inorganic carbon (dissolved CO2, H2CO3, HCO3-, and CO32-) generated upon mineralization of primary producers (PP) and dissolved organic matter (DOM). The aquatic processes leading to inorganic carbon are substantially affected by increased DOM and nutrients via terrestrial runoff, acidic rainfall, increased PP and algal blooms, nitrification, denitrification, sulfate reduction, global warming (GW), and by atmospheric CO2 itself through enhanced photosynthesis. They are consecutively associated with enhanced ocean acidification, hypoxia in acidified deeper seawater, pathogens, algal toxins, oxidative stress by reactive oxygen species, and thermal stress caused by longer stratification periods as an effect of GW. We discuss the mechanistic insights into the aforementioned processes and pH changes, with particular focus on processes taking place with different timescales (including the diurnal one) in surface and subsurface seawater. This review also discusses these collective influences to assess their potential detrimental effects to marine organisms, and of ecosystem processes and services. Our review of the effects operating in synergy with ocean acidification will provide a broad insight into the potential impact of acidification itself on biological processes. The foreseen danger to marine organisms by acidification is in fact expected to be amplified by several concurrent and interacting phenomena.

Reviews and Syntheses: Ocean acidification and its potential impacts on marine ecosystems

NASA Astrophysics Data System (ADS)

Mostofa, K. M. G.; Liu, C.-Q.; Zhai, W. D.; Minella, M.; Vione, D.; Gao, K.; Minakata, D.; Arakaki, T.; Yoshioka, T.; Hayakawa, K.; Konohira, E.; Tanoue, E.; Akhand, A.; Chanda, A.; Wang, B.; Sakugawa, H.

2015-07-01

Ocean acidification, a complex phenomenon that lowers seawater pH, is the net outcome of several contributions. They include the dissolution of increasing atmospheric CO2 that adds up with dissolved inorganic carbon (dissolved CO2, H2CO3, HCO3-, and CO32-) generated upon mineralization of primary producers (PP) and dissolved organic matter (DOM). The aquatic processes leading to inorganic carbon are substantially affected by increased DOM and nutrients via terrestrial runoff, acidic rainfall, increased PP and algal blooms, nitrification, denitrification, sulfate reduction, global warming (GW), and by atmospheric CO2 itself through enhanced photosynthesis. They are consecutively associated with enhanced ocean acidification, hypoxia in acidified deeper seawater, pathogens, algal toxins, oxidative stress by reactive oxygen species, and thermal stress caused by longer stratification periods as an effect of GW. We discuss the mechanistic insights into the aforementioned processes and pH changes, with particular focus on processes taking place with different time scales (including the diurnal one) in surface and subsurface seawater. This review also discusses these collective influences to assess their potential detrimental effects to marine organisms, and of ecosystem processes and services. Our review of the effects operating in synergy with ocean acidification will provide a broad insight into the potential impact of acidification itself on biological processes. The foreseen danger to marine organisms by acidification is in fact expected to be amplified by several concurrent and interacting phenomena.

Comparison of Sea-Air CO2 Flux Estimates Using Satellite-Based Versus Mooring Wind Speed Data

NASA Astrophysics Data System (ADS)

Sutton, A. J.; Sabine, C. L.; Feely, R. A.; Wanninkhof, R. H.

2016-12-01

The global ocean is a major sink of anthropogenic CO2, absorbing approximately 27% of CO2 emissions since the beginning of the industrial revolution. Any variation or change in the ocean CO2 sink has implications for future climate. Observations of sea-air CO2 flux have relied primarily on ship-based underway measurements of partial pressure of CO2 (pCO2) combined with satellite, model, or multi-platform wind products. Direct measurements of ΔpCO2 (seawater - air pCO2) and wind speed from moored platforms now allow for high-resolution CO2 flux time series. Here we present a comparison of CO2 flux calculated from moored ΔpCO2 measured on four moorings in different biomes of the Pacific Ocean in combination with: 1) Cross-Calibrated Multi-Platform (CCMP) winds or 2) wind speed measurements made on ocean reference moorings excluded from the CCMP dataset. Preliminary results show using CCMP winds overestimates CO2 flux on average by 5% at the Kuroshio Extension Observatory, Ocean Station Papa, WHOI Hawaii Ocean Timeseries Station, and Stratus. In general, CO2 flux seasonality follows patterns of seawater pCO2 and SST with periods of CO2 outgassing during summer and CO2 uptake during winter at these locations. Any offsets or seasonal biases in CCMP winds could impact global ocean sink estimates using this data product. Here we present patterns and trends between the two CO2 flux estimates and discuss the potential implications for tracking variability and change in global ocean CO2 uptake.

Biofilm-like properties of the sea surface and predicted effects on air-sea CO2 exchange

NASA Astrophysics Data System (ADS)

Wurl, Oliver; Stolle, Christian; Van Thuoc, Chu; The Thu, Pham; Mari, Xavier

2016-05-01

Because the sea surface controls various interactions between the ocean and the atmosphere, it has a profound function for marine biogeochemistry and climate regulation. The sea surface is the gateway for the exchange of climate-relevant gases, heat and particles. Thus, in order to determine how the ocean and the atmosphere interact and respond to environmental changes on a global scale, the characterization and understanding of the sea surface are essential. The uppermost part of the water column is defined as the sea-surface microlayer and experiences strong spatial and temporal dynamics, mainly due to meteorological forcing. Wave-damped areas at the sea surface are caused by the accumulation of surface-active organic material and are defined as slicks. Natural slicks are observed frequently but their biogeochemical properties are poorly understood. In the present study, we found up to 40 times more transparent exopolymer particles (TEP), the foundation of any biofilm, in slicks compared to the underlying bulk water at multiple stations in the North Pacific, South China Sea, and Baltic Sea. We found a significant lower enrichment of TEP (up to 6) in non-slick sea surfaces compared to its underlying bulk water. Moreover, slicks were characterized by a large microbial biomass, another shared feature with conventional biofilms on solid surfaces. Compared to non-slick samples (avg. pairwise similarity of 70%), the community composition of bacteria in slicks was increasingly (avg. pairwise similarity of 45%) different from bulk water communities, indicating that the TEP-matrix creates specific environments for its inhabitants. We, therefore, conclude that slicks can feature biofilm-like properties with the excessive accumulation of particles and microbes. We also assessed the potential distribution and frequency of slick-formation in coastal and oceanic regions, and their effect on air-sea CO2 exchange based on literature data. We estimate that slicks can reduce CO2 fluxes by up to 15%, and, therefore, play important local and regional roles in regulating air-sea interactions.

Exploring the reversibility of marine climate change impacts in temperature overshoot scenarios

NASA Astrophysics Data System (ADS)

Zickfeld, K.; Li, X.; Tokarska, K.; Kohfeld, K. E.

2017-12-01

Artificial carbon dioxide removal (CDR) from the atmosphere has been proposed as a measure for mitigating climate change and restoring the climate system to a `safe' state after overshoot. Previous studies have demonstrated that the changes in surface air temperature due to anthropogenic CO2 emissions can be reversed through CDR, while some oceanic properties, for example thermosteric sea level rise, show a delay in their response to CDR. This research aims to investigate the reversibility of changes in ocean conditions after implementation of CDR with a focus on ocean biogeochemical properties. To achieve this, we analyze climate model simulations based on two sets of emission scenarios. We first use RCP2.6 and its extension until year 2300 as the reference scenario and design several temperature and cumulative CO2 emissions "overshoot" scenarios based on other RCPs, which represents cases with less ambitious mitigation policies in the near term that temporarily exceed the 2 °C target adopted by the Paris Agreement. In addition, we use a set of emission scenarios with a reference scenario limiting warming to 1.5°C in the long term and two overshoot scenarios. The University of Victoria Earth System Climate Model (UVic ESCM), a climate model of intermediate complexity, is forced with these emission scenarios. We compare the response of select ocean variables (seawater temperature, pH, dissolved oxygen) in the overshoot scenarios to that in the respective reference scenario at the time the same amount of cumulative emissions is achieved. Our results suggest that the overshoot and subsequent return to a reference CO2 cumulative emissions level would leave substantial impacts on the marine environment. Although the changes in global mean sea surface variables (temperature, pH and dissolved oxygen) are largely reversible, global mean ocean temperature, dissolved oxygen and pH differ significantly from those in the reference scenario. Large ocean areas exhibit temperature increase and pH and dissolved oxygen decrease relative to the reference scenario without cumulative CO2 emissions overshoot. Furthermore, our results show that the higher the level of overshoot, the lower the reversibility of changes in the marine environment.

Modeling pCO2 variability in the Gulf of Mexico

NASA Astrophysics Data System (ADS)

Xue, Z.; He, R.; Fennel, K.; Cai, W.-J.; Lohrenz, S.; Huang, W.-J.; Tian, H.

2014-08-01

A three-dimensional coupled physical-biogeochemical model was used to simulate and examine temporal and spatial variability of surface pCO2 in the Gulf of Mexico (GoM). The model is driven by realistic atmospheric forcing, open boundary conditions from a data-assimilative global ocean circulation model, and observed freshwater and terrestrial nutrient and carbon input from major rivers. A seven-year model hindcast (2004-2010) was performed and was validated against in situ measurements. The model revealed clear seasonality in surface pCO2. Based on the multi-year mean of the model results, the GoM is an overall CO2 sink with a flux of 1.34 × 1012 mol C yr-1, which, together with the enormous fluvial carbon input, is balanced by the carbon export through the Loop Current. A sensitivity experiment was performed where all biological sources and sinks of carbon were disabled. In this simulation surface pCO2 was elevated by ~ 70 ppm, providing the evidence that biological uptake is a primary driver for the observed CO2 sink. The model also provided insights about factors influencing the spatial distribution of surface pCO2 and sources of uncertainty in the carbon budget.

Modeling pCO2 Variability in the Gulf of Mexico

NASA Astrophysics Data System (ADS)

Xue, Z. G.; He, R.; Fennel, K.; Cai, W. J.; Lohrenz, S. E.; Huang, W. J.; Tian, H.

2014-12-01

A three-dimensional coupled physical-biogeochemical model was used to simulate and examine temporal and spatial variability of surface pCO2 in the Gulf of Mexico (GoM). The model is driven by realistic atmospheric forcing, open boundary conditions from a data-assimilative global ocean circulation model, and observed freshwater and terrestrial nutrient and carbon input from major rivers. A seven-year model hindcast (2004-2010) was performed and was validated against in situ measurements. The model revealed clear seasonality in surface pCO2. Based on the multi-year mean of the model results, the GoM is an overall CO2 sink with a flux of 1.34 × 1012 mol C yr-1, which, together with the enormous fluvial carbon input, is balanced by the carbon export through the Loop Current. A sensitivity experiment was performed where all biological sources and sinks of carbon were disabled. In this simulation surface pCO2 was elevated by ~70 ppm, providing the evidence that biological uptake is a primary driver for the observed CO2 sink. The model also provided insights about factors influencing the spatial distribution of surface pCO2 and sources of uncertainty in the carbon budget.

An energetic perspective on hydrological cycle changes in the Geoengineering Model Intercomparison Project

NASA Astrophysics Data System (ADS)

Kravitz, Ben; Rasch, Philip J.; Forster, Piers M.; Andrews, Timothy; Cole, Jason N. S.; Irvine, Peter J.; Ji, Duoying; Kristjánsson, Jón Egill; Moore, John C.; Muri, Helene; Niemeier, Ulrike; Robock, Alan; Singh, Balwinder; Tilmes, Simone; Watanabe, Shingo; Yoon, Jin-Ho

2013-12-01

of surface and atmospheric energy budget responses to CO2 and solar forcings can be used to reveal mechanisms of change in the hydrological cycle. We apply this energetic perspective to output from 11 fully coupled atmosphere-ocean general circulation models simulating experiment G1 of the Geoengineering Model Intercomparison Project (GeoMIP), which achieves top-of-atmosphere energy balance between an abrupt quadrupling of CO2 from preindustrial levels (abrupt4xCO2) and uniform solar irradiance reduction. We divide the climate system response into a rapid adjustment, in which climate response is due to adjustment of the atmosphere and land surface on short time scales, and a feedback response, in which the climate response is predominantly due to feedback related to global mean temperature changes. Global mean temperature change is small in G1, so the feedback response is also small. G1 shows a smaller magnitude of land sensible heat flux rapid adjustment than in abrupt4xCO2 and a larger magnitude of latent heat flux adjustment, indicating a greater reduction of evaporation and less land temperature increase than abrupt4xCO2. The sum of surface flux changes in G1 is small, indicating little ocean heat uptake. Using an energetic perspective to assess precipitation changes, abrupt4xCO2 shows decreased mean evaporative moisture flux and increased moisture convergence, particularly over land. However, most changes in precipitation in G1 are in mean evaporative flux, suggesting that changes in mean circulation are small.

Global Autocorrelation Scales of the Partial Pressure of Oceanic CO2

NASA Technical Reports Server (NTRS)

Li, Zhen; Adamec, David; Takahashi, Taro; Sutherland, Stewart C.

2004-01-01

A global database of approximately 1.7 million observations of the partial pressure of carbon dioxide in surface ocean waters (pCO2) collected between 1970 and 2003 is used to estimate its spatial autocorrelation structure. The patterns of the lag distance where the autocorrelation exceeds 0.8 is similar to patterns in the spatial distribution of the first baroclinic Rossby radius of deformation indicating that ocean circulation processes play a significant role in determining the spatial variability of pCO2. For example, the global maximum of the distance at which autocorrelations exceed 0.8 averages about 140 km in the equatorial Pacific. Also, the lag distance at which the autocorrelation exceed 0.8 is greater in the vicinity of the Gulf Stream than it is near the Kuroshio, approximately 50 km near the Gulf Stream as opposed to 20 km near the Kuroshio. Separate calculations for times when the sun is north and south of the equator revealed no obvious seasonal dependence of the spatial autocorrelation scales. The pCO2 measurements at Ocean Weather Station (OWS) 'P', in the eastern subarctic Pacific (50 N, 145 W) is the only fixed location where an uninterrupted time series of sufficient length exists to calculate a meaningful temporal autocorrelation function for lags greater than a few days. The estimated temporal autocorrelation function at OWS 'P', is highly variable. A spectral analysis of the longest four pCO2 time series indicates a high level of variability occurring over periods from the atmospheric synoptic to the maximum length of the time series, in this case 42 days. It is likely that a relative peak in variability with a period of 3-6 days is related to atmospheric synoptic period variability and ocean mixing events due to wind stirring. However, the short length of available time series makes identifying temporal relationships between pCO2 and atmospheric or ocean processes problematic.

Global Carbon Cycle Modeling in GISS ModelE2 GCM

NASA Astrophysics Data System (ADS)

Aleinov, I. D.; Kiang, N. Y.; Romanou, A.; Romanski, J.

2014-12-01

Consistent and accurate modeling of the Global Carbon Cycle remains one of the main challenges for the Earth System Models. NASA Goddard Institute for Space Studies (GISS) ModelE2 General Circulation Model (GCM) was recently equipped with a complete Global Carbon Cycle algorithm, consisting of three integrated components: Ent Terrestrial Biosphere Model (Ent TBM), Ocean Biogeochemistry Module and atmospheric CO2 tracer. Ent TBM provides CO2 fluxes from the land surface to the atmosphere. Its biophysics utilizes the well-known photosynthesis functions of Farqhuar, von Caemmerer, and Berry and Farqhuar and von Caemmerer, and stomatal conductance of Ball and Berry. Its phenology is based on temperature, drought, and radiation fluxes, and growth is controlled via allocation of carbon from labile carbohydrate reserve storage to different plant components. Soil biogeochemistry is based on the Carnegie-Ames-Stanford (CASA) model of Potter et al. Ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM), computes prognostic distributions for biotic and abiotic fields that influence the air-sea flux of CO2 and the deep ocean carbon transport and storage. Atmospheric CO2 is advected with a quadratic upstream algorithm implemented in atmospheric part of ModelE2. Here we present the results for pre-industrial equilibrium and modern transient simulations and provide comparison to available observations. We also discuss the process of validation and tuning of particular algorithms used in the model.

Assessing Regional Scale Fluxes of Mass, Momentum, and Energy with Small Environmental Research Aircraft

NASA Astrophysics Data System (ADS)

Zulueta, Rommel Callejo

Natural ecosystems are rarely structurally or functionally homogeneous. This is true for the complex coastal regions of Magdalena Bay, Baja California Sur, Mexico, and the Barrow Peninsula on the Arctic Coastal Plain of Alaska. The coastal region of Magdalena Bay is comprised of the Pacific coastal ocean, eutrophic lagoon, mangroves, and desert ecosystems all adjacent and within a few kilometers, while the Barrow Peninsula is a mosaic of small ponds, thaw lakes, different aged vegetated thaw-lake basins ( VDTLBs ) and interstitial tundra which have been dynamically formed by both short- and long-term processes. We used a combination of tower- and small environmental research aircraft (SERA)-based eddy covariance measurements to characterize the spatial and temporal patterns of CO2, latent, and sensible heat fluxes along with MODIS NDVI, and land surface information, to scale the SERA-based CO2 fluxes up to the regional scale. In the first part of this research, the spatial variability in ecosystem fluxes from the Pacific coastal ocean, eutrophic lagoon, mangroves, and desert areas of northern Magdalena Bay were studied. SERA-derived average midday CO2 fluxes from the desert showed a slight uptake of -1.32 mumol CO2 m-2 s-1, the coastal ocean also showed uptake of -3.48 mumol CO2 m-2 s -1, and the lagoon mangroves showed the highest uptake of -8.11 mumol CO2 m-2 s-1. Additional simultaneous measurements of NDVI allowed simple linear modeling of CO2 flux as a function of NDVI for the mangroves of the Magdalena Bay region. In the second part of this research, the spatial variability of ecosystem fluxes across the 1802 km2 Barrow Peninsula region was studied. During typical 2006 summer conditions, the midday hourly CO2 flux over the region was -2.04 x 105 kgCO2 hr-1. The CO2 fluxes among the interstitial tundra, Ancient and Old VDTLBs, as well as between the Medium and Young VDTLBs were not significantly different. Combined, the interstitial tundra and Old and Ancient VDTLBs, represent ˜67% of the Barrow Peninsula surface area, accounting for ˜59% of the regional flux signal. Though the Medium and Young VDTLBs represent ˜11% of the surface area, they account for a large portion, ˜35%, of the total regional flux. The remaining ˜22% of the surface area are lakes and contributed the remaining ˜6% of the total regional flux. Previous studies treated vegetated areas of the region as a single surface type with measurements from a few study sites; doing so could underestimate the regional flux by ˜22%. The San Diego State University Sky Arrow 650TCN Environmental Research Aircraft proved to be an effective tool in characterizing land-atmosphere fluxes of energy, CO2 and water across heterogeneous landscapes at the scale of 1 km, and was capable of discriminating fluxes from the various ecosystem and land surface types a few kilometers distant. Here, we demonstrate that SERA-based approaches have the ability to cover large spatial scales while measuring the turbulent fluxes across a number of surfaces and combined with ground- and satellite-based measurements provide a valuable tool for both scaling and validation of regional-scale fluxes.

Reviews and syntheses: An empirical spatiotemporal description of the global surface-atmosphere carbon fluxes: opportunities and data limitations

NASA Astrophysics Data System (ADS)

Zscheischler, Jakob; Mahecha, Miguel D.; Avitabile, Valerio; Calle, Leonardo; Carvalhais, Nuno; Ciais, Philippe; Gans, Fabian; Gruber, Nicolas; Hartmann, Jens; Herold, Martin; Ichii, Kazuhito; Jung, Martin; Landschützer, Peter; Laruelle, Goulven G.; Lauerwald, Ronny; Papale, Dario; Peylin, Philippe; Poulter, Benjamin; Ray, Deepak; Regnier, Pierre; Rödenbeck, Christian; Roman-Cuesta, Rosa M.; Schwalm, Christopher; Tramontana, Gianluca; Tyukavina, Alexandra; Valentini, Riccardo; van der Werf, Guido; West, Tristram O.; Wolf, Julie E.; Reichstein, Markus

2017-08-01

Understanding the global carbon (C) cycle is of crucial importance to map current and future climate dynamics relative to global environmental change. A full characterization of C cycling requires detailed information on spatiotemporal patterns of surface-atmosphere fluxes. However, relevant C cycle observations are highly variable in their coverage and reporting standards. Especially problematic is the lack of integration of the carbon dioxide (CO2) exchange of the ocean, inland freshwaters and the land surface with the atmosphere. Here we adopt a data-driven approach to synthesize a wide range of observation-based spatially explicit surface-atmosphere CO2 fluxes from 2001 to 2010, to identify the state of today's observational opportunities and data limitations. The considered fluxes include net exchange of open oceans, continental shelves, estuaries, rivers, and lakes, as well as CO2 fluxes related to net ecosystem productivity, fire emissions, loss of tropical aboveground C, harvested wood and crops, as well as fossil fuel and cement emissions. Spatially explicit CO2 fluxes are obtained through geostatistical and/or remote-sensing-based upscaling, thereby minimizing biophysical or biogeochemical assumptions encoded in process-based models. We estimate a bottom-up net C exchange (NCE) between the surface (land, ocean, and coastal areas) and the atmosphere. Though we provide also global estimates, the primary goal of this study is to identify key uncertainties and observational shortcomings that need to be prioritized in the expansion of in situ observatories. Uncertainties for NCE and its components are derived using resampling. In many regions, our NCE estimates agree well with independent estimates from other sources such as process-based models and atmospheric inversions. This holds for Europe (mean ± 1 SD: 0.8 ± 0.1 PgC yr-1, positive numbers are sources to the atmosphere), Russia (0.1 ± 0.4 PgC yr-1), East Asia (1.6 ± 0.3 PgC yr-1), South Asia (0.3 ± 0.1 PgC yr-1), Australia (0.2 ± 0.3 PgC yr-1), and most of the Ocean regions. Our NCE estimates give a likely too large CO2 sink in tropical areas such as the Amazon, Congo, and Indonesia. Overall, and because of the overestimated CO2 uptake in tropical lands, our global bottom-up NCE amounts to a net sink of -5.4 ± 2.0 PgC yr-1. By contrast, the accurately measured mean atmospheric growth rate of CO2 over 2001-2010 indicates that the true value of NCE is a net CO2 source of 4.3 ± 0.1 PgC yr-1. This mismatch of nearly 10 PgC yr-1 highlights observational gaps and limitations of data-driven models in tropical lands, but also in North America. Our uncertainty assessment provides the basis for setting priority regions where to increase carbon observations in the future. High on the priority list are tropical land regions, which suffer from a lack of in situ observations. Second, extensive pCO2 data are missing in the Southern Ocean. Third, we lack observations that could enable seasonal estimates of shelf, estuary, and inland water-atmosphere C exchange. Our consistent derivation of data uncertainties could serve as prior knowledge in multicriteria optimization such as the Carbon Cycle Data Assimilation System (CCDAS) and atmospheric inversions, without over- or under-stating bottom-up data credibility. In the future, NCE estimates of carbon sinks could be aggregated at national scale to compare with the official national inventories of CO2 fluxes in the land use, land use change, and forestry sector, upon which future emission reductions are proposed.

Coralline Algal Skeletal δ13C as a Multicentury Recorder of Carbon Dynamics in the Labrador Sea

NASA Astrophysics Data System (ADS)

Meng Xiao Hou, Alicia; Halfar, Jochen; Adey, Walter; Wortmann, Ulrich; Williams, Branwen; Chan, Phoebe

2017-04-01

The introduction of isotopically light carbon due to the emission of fossil fuel derived CO2 since the beginning of the industrial revolution has decreased δ13C in the atmosphere and oceans (termed the δ13C Suess effect). Approximately 48% of CO2 emissions from fossil fuel combustion and cement manufacturing were taken up by the oceans during the period 1800 to 1994, decreasing the δ13C of the oceanic dissolved inorganic carbon reservoir (DIC). Rates of oceanic carbon uptake vary regionally in response to several factors including ocean circulation, productivity, and water temperature. Despite the enhanced CO2-uptake ability of the North Atlantic Ocean, carbon fluxes of surface ocean waters in high latitude regions are relatively poorly understood compared to tropical oceans. Therefore, century-scale, high-resolution marine climate archives from high latitude regions are needed in order to better understand both preindustrial carbon isotope dynamics as well as carbon isotope changes in response to anthropogenic forcing. Here, we present a 193-year record of δ13C obtained from the annual growth bands of a long-lived calcified coralline alga collected off the coast of central Labrador, near Kingitok Island, Canada (55.3983° N, 59.8467° W) to observe regional changes in carbon isotopes beginning in the preindustrial period. The algal δ13C record demonstrates an overall decreasing trend of -0.006‰/year from 1819 (1.15‰) to 2012 (-0.013‰), with the fastest rate of decrease (-0.032‰/year) occurring from 1960 (1.63‰) to 2012 (-0.013‰). Comparisons of the coralline algal δ13C record to a bivalve δ13C record (r = 0.30, p < 0.00007) and an atmospheric CO2 δ13C record from compiled ice core and direct measurement data (r =0.35, p < 0.00000051) displays a good correspondence of century-scale δ13C trends. The coralline algal record is interpreted as representing a combination of changes in primary productivity, which dominates the signal during the preindustrial portion of the record (1819 to 1850), and the increasing atmospheric input of anthropogenically derived light carbon post 1850. The latter effect becomes increasingly important in the younger portion of the coralline algal record. In order to study changes in surface ocean productivity, we therefore mathematically removed the Suess effect from 1850 onwards using a previously established Suess Effect Correction Factor. The Suess corrected algal δ13C record now exhibits an overall increasing trend from 1850 to 2012. We interpret this as reflecting an ongoing increase in Labrador Sea primary productivity, which is supported by observed recent increases in ocean productivity associated with the decline in sea ice cover in the Arctic and Subarctic oceans. Considering the important economic value of enormous fisheries supported by the Arctic and sub-Arctic oceans and the role of this region as a significant CO2 sink, it is necessary to quantify changes in primary productivity as well as the rate of oceanic uptake of anthropogenic CO2, both of which are reflected in changes in the carbon isotope composition of oceanic DIC.

Improved Surface and Tropospheric Temperatures Determined Using Only Shortwave Channels: The AIRS Science Team Version-6 Retrieval Algorithm

NASA Technical Reports Server (NTRS)

Susskind, Joel; Blaisdell, John; Iredell, Lena

2011-01-01

The Goddard DISC has generated products derived from AIRS/AMSU-A observations, starting from September 2002 when the AIRS instrument became stable, using the AIRS Science Team Version-5 retrieval algorithm. The AIRS Science Team Version-6 retrieval algorithm will be finalized in September 2011. This paper describes some of the significant improvements contained in the Version-6 retrieval algorithm, compared to that used in Version-5, with an emphasis on the improvement of atmospheric temperature profiles, ocean and land surface skin temperatures, and ocean and land surface spectral emissivities. AIRS contains 2378 spectral channels covering portions of the spectral region 650 cm(sup -1) (15.38 micrometers) - 2665 cm(sup -1) (3.752 micrometers). These spectral regions contain significant absorption features from two CO2 absorption bands, the 15 micrometers (longwave) CO2 band, and the 4.3 micrometers (shortwave) CO2 absorption band. There are also two atmospheric window regions, the 12 micrometer - 8 micrometer (longwave) window, and the 4.17 micrometer - 3.75 micrometer (shortwave) window. Historically, determination of surface and atmospheric temperatures from satellite observations was performed using primarily observations in the longwave window and CO2 absorption regions. According to cloud clearing theory, more accurate soundings of both surface skin and atmospheric temperatures can be obtained under partial cloud cover conditions if one uses observations in longwave channels to determine coefficients which generate cloud cleared radiances R(sup ^)(sub i) for all channels, and uses R(sup ^)(sub i) only from shortwave channels in the determination of surface and atmospheric temperatures. This procedure is now being used in the AIRS Version-6 Retrieval Algorithm. Results are presented for both daytime and nighttime conditions showing improved Version-6 surface and atmospheric soundings under partial cloud cover.

Changes in CaCO3 Burial Trump the Biological Pump

NASA Astrophysics Data System (ADS)

Toggweiler, J.; Dunne, J. P.

2008-12-01

The dramatic increases in atmospheric CO2 at the ends of ice ages are usually attributed to a one-two punch coming from the ocean. First, a weakened biological pump vents organically cycled CO2 from the deep ocean via changes in the ventilation of the deep ocean around Antarctica. The initial CO2 increase is then augmented by an enhancement of CaCO3 burial due to a process called CaCO3 compensation (after Broecker, W. S and T.-H. Peng, Global Biogeochem. Cycles, 1, 15-29, 1987). Here, we argue that the importance of the biological pump has been exaggerated. The main effect comes from circulation-induced changes in the burial of CaCO3. As shown in a recent paper by Andreas Schmittner and co-authors (Schmittner, A., E. Brook and J. Ahn, Impact of the ocean's overturning circulation on atmospheric CO2, in Ocean Circulation: Mechanisms and Impacts, Geophys. Monogr. 173, A. Schmittner, J. Chiang, and S. Hemming, eds., pp. 209-246, AGU, 2007) changes in the ventilation of the deep ocean around Antarctica gave rise to 20-30 ppm increases in atmospheric CO2 every 5,000-7,000 years during isotope stages 3 and 4 (30,000 to 70,000 years ago). None of these venting events gave rise to a compensation response. Meanwhile, Jaccard et al. (Science, 308, 1003-1006, 2005) show that all the big CO2 increases during terminations through stage 11 were accompanied by huge increases in CaCO3 burial. This suggests that the enhanced burial of CaCO3 is obligatory rather than compensatory with respect to the dramatic CO2 increases. Broecker and Peng's compensation idea is based on an assumption that the rain of CaCO3 to the sea floor is the same everywhere. More specifically, it assumes that there is no spatial correlation between the production of CaCO3 at the surface and the burial on the sea floor. We find instead that the production and burial of CaCO3 tend to be co-located in regional "hot spots" and that burial in the hot spots balances the input of Ca++ and HCO3- ions in rivers. The hot spots can also move from place to place in response to changes in circulation. The main hot spots today are the eastern Atlantic and southern Indian; the main hot spot during the last glacial was the equatorial Pacific. Renewed deep-water formation in the Atlantic at the end of the last ice age shifted the locus of CaCO3 burial back to the Atlantic and southern Indian and led to a huge drawdown in global alkalinity, which is ongoing today and accounts for most of the deglacial rise in atmospheric CO2.

Seasonality of biological and physical controls on surface ocean CO2 from hourly observations at the Southern Ocean Time Series site south of Australia

NASA Astrophysics Data System (ADS)

Shadwick, E. H.; Trull, T. W.; Tilbrook, B.; Sutton, A. J.; Schulz, E.; Sabine, C. L.

2015-02-01

The Subantarctic Zone (SAZ), which covers the northern half of the Southern Ocean between the Subtropical and Subantarctic Fronts, is important for air-sea CO2 exchange, ventilation of the lower thermocline, and nutrient supply for global ocean productivity. Here we present the first high-resolution autonomous observations of mixed layer CO2 partial pressure (pCO2) and hydrographic properties covering a full annual cycle in the SAZ. The amplitude of the seasonal cycle in pCO2 (˜60 μatm), from near-atmospheric equilibrium in late winter to ˜330 μatm in midsummer, results from opposing physical and biological drivers. Decomposing these contributions demonstrates that the biological control on pCO2 (up to 100 μatm), is 4 times larger than the thermal component and driven by annual net community production of 2.45 ± 1.47 mol C m-2 yr-1. After the summer biological pCO2 depletion, the return to near-atmospheric equilibrium proceeds slowly, driven in part by autumn entrainment into a deepening mixed layer and achieving full equilibration in late winter and early spring as respiration and advection complete the annual cycle. The shutdown of winter convection and associated mixed layer shoaling proceeds intermittently, appearing to frustrate the initiation of production. Horizontal processes, identified from salinity anomalies, are associated with biological pCO2 signatures but with differing impacts in winter (when they reflect far-field variations in dissolved inorganic carbon and/or biomass) and summer (when they suggest promotion of local production by the relief of silicic acid or iron limitation). These results provide clarity on SAZ seasonal carbon cycling and demonstrate that the magnitude of the seasonal pCO2 cycle is twice as large as that in the subarctic high-nutrient, low-chlorophyll waters, which can inform the selection of optimal global models in this region.

Spatial and temporal variability of seawater pCO2 within the Canadian Arctic Archipelago and Baffin Bay during the summer and autumn 2011

NASA Astrophysics Data System (ADS)

Geilfus, N.-X.; Pind, M. L.; Else, B. G. T.; Galley, R. J.; Miller, L. A.; Thomas, H.; Gosselin, M.; Rysgaard, S.; Wang, F.; Papakyriakou, T. N.

2018-03-01

The partial pressure of CO2 in surface water (pCO2sw) measured within the Canadian Arctic Archipelago (CAA) and Baffin Bay was highly variable with values ranging from strongly undersaturated (118 μatm) to slightly supersaturated (419 μatm) with respect to the atmospheric levels ( 386 μatm) during summer and autumn 2011. During summer, melting sea ice contributed to cold and fresh surface water and enhanced the ice-edge bloom, resulting in strong pCO2sw undersaturation. Coronation Gulf was the only area with supersaturated pCO2sw, likely due to warm CO2-enriched freshwater input from the Coppermine River. During autumn, the entire CAA (including Coronation Gulf) was undersaturated, despite generally increasing pCO2sw. Coronation Gulf was the one place where pCO2sw decreased, likely due to seasonal reduction in discharge from the Coppermine River and the decreasing sea surface temperature. The seasonal summer-to-autumn increase in pCO2sw across the archipelago is attributed in part to the continuous uptake of atmospheric CO2 through both summer and autumn and to the seasonal deepening of the surface mixed layer, bringing CO2-rich waters to the surface. These observations demonstrate how freshwater from sea ice melt and rivers affect pCO2sw differently. The general pCO2sw undersaturation during summer-autumn 2011 throughout the CAA and Baffin Bay give an estimated net oceanic sink for atmospheric CO2 over the study period of 11.4 mmol CO2 m-2 d-1, assuming no sea-air CO2 flux exchange across the sea-ice covered areas.

Vegetation and Carbon Cycle Dynamics in the High-Resolution Transient Holocene Simulations Using the MPI Earth System Model

NASA Astrophysics Data System (ADS)

Brovkin, V.; Lorenz, S.; Raddatz, T.; Claussen, M.; Dallmeyer, A.

2017-12-01

One of the interesting periods to investigate a climatic role of terrestrial biosphere is the Holocene, when, despite of the relatively steady global climate, the atmospheric CO2 grew by about 20 ppm from 7 kyr BP to pre-industrial. We use a new setup of the Max Planck Institute Earth System Model MPI-ESM1 consisting of the latest version of the atmospheric model ECHAM6, including the land surface model JSBACH3 with carbon cycle and vegetation dynamics, coupled to the ocean circulation model MPI-OM, which includes the HAMOCC model of ocean biogeochemistry. The model has been run for several simulations over the Holocene period of the last 8000 years under the forcing data sets of orbital insolation, atmospheric greenhouse gases, volcanic aerosols, solar irradiance and stratospheric ozone, as well as land-use changes. In response to this forcing, the land carbon storage increased by about 60 PgC between 8 and 4 kyr BP, stayed relatively constant until 2 kyr BP, and decreased by about 90 PgC by 1850 AD due to land use changes. At 8 kyr BP, vegetation cover was much denser in Africa, mainly due to increased rainfall in response to the orbital forcing. Boreal forests moved northward in both, North America and Eurasia. The boreal forest expansion in North America is much less pronounced than in Eurasia. Simulated physical ocean fields, including surface temperatures and meridional overturning, do not change substantially in the Holocene. Carbonate ion concentration in deep ocean decreases in both, prescribed and interactive CO2simulations. Comparison with available proxies for terrestrial vegetation and for the ocean carbonate chemistry will be presented. Vegetation and soil carbon changes significantly affected atmospheric CO2 during the periods of strong volcanic eruptions. In response to the eruption-caused cooling, the land initially stores more carbon as respiration decreases, but then it releases even more carbon die to productivity decrease. This decadal-scale variability helps to quantify the vegetation and land carbon feedbacks during the past periods when the temporal resolution of the ice-core CO2 record is not sufficient to capture fast CO2 variations. From a set of Holocene simulations with prescribed or interactive atmospheric CO2, we get estimates of climate-carbon feedback useful for future climate studies.

Carbonate saturation state of surface waters in the Ross Sea and Southern Ocean: controls and implications for the onset of aragonite undersaturation

NASA Astrophysics Data System (ADS)

DeJong, H. B.; Dunbar, R. B.; Mucciarone, D. A.; Koweek, D.

2016-02-01

Predicting when surface waters of the Ross Sea and Southern Ocean will become undersaturated with respect to biogenic carbonate minerals is challenging in part due to the lack of baseline high resolution carbon system data. Here we present 1700 surface total alkalinity measurements from the Ross Sea and along a transect between the Ross Sea and southern Chile from the austral autumn (February-March 2013). We calculate the saturation state of aragonite (ΩAr) and calcite (ΩCa) using measured total alkalinity and pCO2. In the Ross Sea and south of the Polar Front, variability in carbonate saturation state (Ω) is mainly driven by algal photosynthesis. Freshwater dilution and calcification have minimal influence on Ω variability. We estimate an early spring surface water ΩAr value of 1.2 for the Ross Sea using a total alkalinity-salinity relationship and historical pCO2 measurements. Our results suggest that the Ross Sea is not likely to become undersaturated with respect to aragonite until the year 2070.

Synergistic effects of climate-related variables suggest future physiological impairment in a top oceanic predator.

PubMed

Rosa, Rui; Seibel, Brad A

2008-12-30

By the end of this century, anthropogenic carbon dioxide (CO(2)) emissions are expected to decrease the surface ocean pH by as much as 0.3 unit. At the same time, the ocean is expected to warm with an associated expansion of the oxygen minimum layer (OML). Thus, there is a growing demand to understand the response of the marine biota to these global changes. We show that ocean acidification will substantially depress metabolic rates (31%) and activity levels (45%) in the jumbo squid, Dosidicus gigas, a top predator in the Eastern Pacific. This effect is exacerbated by high temperature. Reduced aerobic and locomotory scope in warm, high-CO(2) surface waters will presumably impair predator-prey interactions with cascading consequences for growth, reproduction, and survival. Moreover, as the OML shoals, squids will have to retreat to these shallower, less hospitable, waters at night to feed and repay any oxygen debt that accumulates during their diel vertical migration into the OML. Thus, we demonstrate that, in the absence of adaptation or horizontal migration, the synergism between ocean acidification, global warming, and expanding hypoxia will compress the habitable depth range of the species. These interactions may ultimately define the long-term fate of this commercially and ecologically important predator.

Synergistic effects of climate-related variables suggest future physiological impairment in a top oceanic predator

PubMed Central

Rosa, Rui; Seibel, Brad A.

2008-01-01

By the end of this century, anthropogenic carbon dioxide (CO2) emissions are expected to decrease the surface ocean pH by as much as 0.3 unit. At the same time, the ocean is expected to warm with an associated expansion of the oxygen minimum layer (OML). Thus, there is a growing demand to understand the response of the marine biota to these global changes. We show that ocean acidification will substantially depress metabolic rates (31%) and activity levels (45%) in the jumbo squid, Dosidicus gigas, a top predator in the Eastern Pacific. This effect is exacerbated by high temperature. Reduced aerobic and locomotory scope in warm, high-CO2 surface waters will presumably impair predator–prey interactions with cascading consequences for growth, reproduction, and survival. Moreover, as the OML shoals, squids will have to retreat to these shallower, less hospitable, waters at night to feed and repay any oxygen debt that accumulates during their diel vertical migration into the OML. Thus, we demonstrate that, in the absence of adaptation or horizontal migration, the synergism between ocean acidification, global warming, and expanding hypoxia will compress the habitable depth range of the species. These interactions may ultimately define the long-term fate of this commercially and ecologically important predator. PMID:19075232

Algal refossilization of atmospheric carbon dioxide. [Contains bibliography

DOE Office of Scientific and Technical Information (OSTI.GOV)

Neushul, M.

1991-07-01

The atmospheric concentration of carbon dioxide (CO{sub 2}) is steadily increasing. With our increasing awareness of the economic and environmental impacts of the greenhouse effects'' of CO{sub 2}, methane and other gases, there is interest in finding new methods to reduce the amounts of these gases in the atmosphere. This study evaluates the possibility that large-scale oceanic cultures of macroalgae (macroscopic seaweeds'') could be used to capture atmospheric CO{sub 2}. It is a design for a marine farm system in which a crop'' of calcareous macroalgae grows attached to, and supported by, floating macroalgae that comprise the farm structure.'' Themore » least complicated, yet feasible, macroalgal farm system appears to be one in which laboratory-propagated calcareous algal epiphytes'' and floating algal basiphytes'' are dispersed together in natural ocean upwelling regions. From there, the plants drift with surface currents to the open ocean and then sink to the sea floor, where the buried carbon is refossilized.'' An important caveat regarding the use of calcareous algae is that the process of calcification may release CO{sub 2} to the atmosphere. There is some evidence that CO{sub 2} is not released by calcification in red calcareous algae, but in contrast many geochemists feel that all biologically -- as well as chemically --mediated calcification processes release CO{sub 2}. A substantial amount of research will be necessary to answer basic questions about algal carbon fixation and biomineralization on one hand, while on the other hand to devise strategies for farming the open ocean. 76 refs., 14 figs., 7 tabs.« less

In-life pteropod shell dissolution as an indicator of past ocean carbonate saturation

NASA Astrophysics Data System (ADS)

Wall-Palmer, Deborah; Smart, Christopher W.; Hart, Malcolm B.

2013-12-01

Recent concern over the effects of ocean acidification upon calcifying organisms has highlighted the aragonitic shelled thecosomatous pteropods as being at a high risk. Both in-situ and laboratory studies have shown that an increased dissolved CO2 concentration, leading to decreased water pH and low carbonate concentration, causes reduced calcification rates and enhanced dissolution in the shells of living pteropods. In fossil records unaffected by post-depositional dissolution, this in-life shell dissolution can be detected. Here we present the first evidence of variations of in-life pteropod shell dissolution due to variations in surface water carbonate concentration during the Late Pleistocene by analysing the surface layer of pteropod shells in marine sediment cores from the Caribbean Sea and Indian Ocean. In-life shell dissolution was determined by applying the Limacina Dissolution Index (LDX) to the sub-tropical pteropod Limacina inflata. Average shell size information shows that high in-life dissolution is accompanied by smaller shell sizes in L. inflata, which may indicate a reduction in calcification rate. Comparison of the LDX profile to Late Pleistocene Vostok atmospheric CO2 concentrations, shows that in-life pteropod dissolution is closely associated to variations in past ocean carbonate saturation. This study confirms the findings of laboratory studies, showing enhanced shell dissolution and reduced calcification in living pteropods when surface ocean carbonate concentrations were lower. Results also demonstrate that oceanic pH levels that were less acidic and changing less rapidly than those predicted for the 21st Century, negatively affected pteropods during the Late Pleistocene.

Calcification response of a key phytoplankton family to millennial-scale environmental change

NASA Astrophysics Data System (ADS)

McClelland, H. L. O.; Barbarin, N.; Beaufort, L.; Hermoso, M.; Ferretti, P.; Greaves, M.; Rickaby, R. E. M.

2016-09-01

Coccolithophores are single-celled photosynthesizing marine algae, responsible for half of the calcification in the surface ocean, and exert a strong influence on the distribution of carbon among global reservoirs, and thus Earth’s climate. Calcification in the surface ocean decreases the buffering capacity of seawater for CO2, whilst photosynthetic carbon fixation has the opposite effect. Experiments in culture have suggested that coccolithophore calcification decreases under high CO2 concentrations ([CO2(aq)]) constituting a negative feedback. However, the extent to which these results are representative of natural populations, and of the response over more than a few hundred generations is unclear. Here we describe and apply a novel rationale for size-normalizing the mass of the calcite plates produced by the most abundant family of coccolithophores, the Noëlaerhabdaceae. On average, ancient populations subjected to coupled gradual increases in [CO2(aq)] and temperature over a few million generations in a natural environment become relatively more highly calcified, implying a positive climatic feedback. We hypothesize that this is the result of selection manifest in natural populations over millennial timescales, so has necessarily eluded laboratory experiments.

Calcification response of a key phytoplankton family to millennial-scale environmental change

PubMed Central

McClelland, H. L. O.; Barbarin, N.; Beaufort, L.; Hermoso, M.; Ferretti, P.; Greaves, M.; Rickaby, R. E. M.

2016-01-01

Coccolithophores are single-celled photosynthesizing marine algae, responsible for half of the calcification in the surface ocean, and exert a strong influence on the distribution of carbon among global reservoirs, and thus Earth’s climate. Calcification in the surface ocean decreases the buffering capacity of seawater for CO2, whilst photosynthetic carbon fixation has the opposite effect. Experiments in culture have suggested that coccolithophore calcification decreases under high CO2 concentrations ([CO2(aq)]) constituting a negative feedback. However, the extent to which these results are representative of natural populations, and of the response over more than a few hundred generations is unclear. Here we describe and apply a novel rationale for size-normalizing the mass of the calcite plates produced by the most abundant family of coccolithophores, the Noëlaerhabdaceae. On average, ancient populations subjected to coupled gradual increases in [CO2(aq)] and temperature over a few million generations in a natural environment become relatively more highly calcified, implying a positive climatic feedback. We hypothesize that this is the result of selection manifest in natural populations over millennial timescales, so has necessarily eluded laboratory experiments. PMID:27677230

The role of internal variability for decadal carbon uptake anomalies in the Southern Ocean

NASA Astrophysics Data System (ADS)

Spring, Aaron; Hi, Hongmei; Ilyina, Tatiana

2017-04-01

The Southern Ocean is a major sink for anthropogenic CO2 emissions and hence it plays an essential role in modulating global carbon cycle and climate change. Previous studies based on observations (e.g., Landschützer et al. 2015) show pronounced decadal variations of carbon uptake in the Southern Ocean in recent decades and this variability is largely driven by internal climate variability. However, due to limited ensemble size of simulations, the variability of this important ocean sink is still poorly assessed by the state-of-the-art earth system models (ESMs). To assess the internal variability of carbon sink in the Southern Ocean, we use a large ensemble of 100 member simulations based on the Max Planck Institute-ESM (MPI-ESM). The large ensemble of simulations is generated via perturbed initial conditions in the ocean and atmosphere. Each ensemble member includes a historical simulation from 1850 to 2005 with an extension until 2100 under Representative Concentration Pathway (RCP) 4.5 future projections. Here we use model simulations from 1980-2015 to compare with available observation-based dataset. We found several ensemble members showing decadal decreasing trends in the carbon sink, which are similar to the trend shown in observations. This result suggests that MPI-ESM large ensemble simulations are able to reproduce decadal variation of carbon sink in the Southern Ocean. Moreover, the decreasing trends of Southern Ocean carbon sink in MPI-ESM are mainly contributed by region between 50-60°S. To understand the internal variability of the air-sea carbon fluxes in the Southern Ocean, we further investigate the variability of underlying processes, such as physical climate variability and ocean biological processes. Our results indicate two main drivers for the decadal decreasing trend of carbon sink: i) Intensified winds enhance upwelling of old carbon-rich waters, this leads to increase of the ocean surface pCO2; ii) Primary production is reduced in area from 50-60°S, probably induced by reduced euphotic water column stability; therefore the biological drawdown of ocean surface pCO2 is weakened accordingly and hence the ocean is in favor of carbon outgassing. Landschützer, et al. (2015): The reinvigoration of the Southern Ocean carbon sink, Science, 349, 1221-1224.

Impact of global warming and rising CO2 levels on coral reef fishes: what hope for the future?

PubMed

Munday, Philip L; McCormick, Mark I; Nilsson, Göran E

2012-11-15

Average sea-surface temperature and the amount of CO(2) dissolved in the ocean are rising as a result of increasing concentrations of atmospheric CO(2). Many coral reef fishes appear to be living close to their thermal optimum, and for some of them, even relatively moderate increases in temperature (2-4°C) lead to significant reductions in aerobic scope. Reduced aerobic capacity could affect population sustainability because less energy can be devoted to feeding and reproduction. Coral reef fishes seem to have limited capacity to acclimate to elevated temperature as adults, but recent research shows that developmental and transgenerational plasticity occur, which might enable some species to adjust to rising ocean temperatures. Predicted increases in P(CO(2)), and associated ocean acidification, can also influence the aerobic scope of coral reef fishes, although there is considerable interspecific variation, with some species exhibiting a decline and others an increase in aerobic scope at near-future CO(2) levels. As with thermal effects, there are transgenerational changes in response to elevated CO(2) that could mitigate impacts of high CO(2) on the growth and survival of reef fishes. An unexpected discovery is that elevated CO(2) has a dramatic effect on a wide range of behaviours and sensory responses of reef fishes, with consequences for the timing of settlement, habitat selection, predator avoidance and individual fitness. The underlying physiological mechanism appears to be the interference of acid-base regulatory processes with brain neurotransmitter function. Differences in the sensitivity of species and populations to global warming and rising CO(2) have been identified that will lead to changes in fish community structure as the oceans warm and becomes more acidic; however, the prospect for acclimation and adaptation of populations to these threats also needs to be considered. Ultimately, it will be the capacity for species to adjust to environmental change over coming decades that will determine the impact of climate change on marine ecosystems.

Food supply confers calcifiers resistance to ocean acidification.

PubMed

Ramajo, Laura; Pérez-León, Elia; Hendriks, Iris E; Marbà, Núria; Krause-Jensen, Dorte; Sejr, Mikael K; Blicher, Martin E; Lagos, Nelson A; Olsen, Ylva S; Duarte, Carlos M

2016-01-18

Invasion of ocean surface waters by anthropogenic CO2 emitted to the atmosphere is expected to reduce surface seawater pH to 7.8 by the end of this century compromising marine calcifiers. A broad range of biological and mineralogical mechanisms allow marine calcifiers to cope with ocean acidification, however these mechanisms are energetically demanding which affect other biological processes (trade-offs) with important implications for the resilience of the organisms against stressful conditions. Hence, food availability may play a critical role in determining the resistance of calcifiers to OA. Here we show, based on a meta-analysis of existing experimental results assessing the role of food supply in the response of organisms to OA, that food supply consistently confers calcifiers resistance to ocean acidification.

Food supply confers calcifiers resistance to ocean acidification

NASA Astrophysics Data System (ADS)

Ramajo, Laura; Pérez-León, Elia; Hendriks, Iris E.; Marbà, Núria; Krause-Jensen, Dorte; Sejr, Mikael K.; Blicher, Martin E.; Lagos, Nelson A.; Olsen, Ylva S.; Duarte, Carlos M.

2016-01-01

Invasion of ocean surface waters by anthropogenic CO2 emitted to the atmosphere is expected to reduce surface seawater pH to 7.8 by the end of this century compromising marine calcifiers. A broad range of biological and mineralogical mechanisms allow marine calcifiers to cope with ocean acidification, however these mechanisms are energetically demanding which affect other biological processes (trade-offs) with important implications for the resilience of the organisms against stressful conditions. Hence, food availability may play a critical role in determining the resistance of calcifiers to OA. Here we show, based on a meta-analysis of existing experimental results assessing the role of food supply in the response of organisms to OA, that food supply consistently confers calcifiers resistance to ocean acidification.

Food supply confers calcifiers resistance to ocean acidification

PubMed Central

Ramajo, Laura; Pérez-León, Elia; Hendriks, Iris E.; Marbà, Núria; Krause-Jensen, Dorte; Sejr, Mikael K.; Blicher, Martin E.; Lagos, Nelson A.; Olsen, Ylva S.; Duarte, Carlos M.

2016-01-01

Invasion of ocean surface waters by anthropogenic CO2 emitted to the atmosphere is expected to reduce surface seawater pH to 7.8 by the end of this century compromising marine calcifiers. A broad range of biological and mineralogical mechanisms allow marine calcifiers to cope with ocean acidification, however these mechanisms are energetically demanding which affect other biological processes (trade-offs) with important implications for the resilience of the organisms against stressful conditions. Hence, food availability may play a critical role in determining the resistance of calcifiers to OA. Here we show, based on a meta-analysis of existing experimental results assessing the role of food supply in the response of organisms to OA, that food supply consistently confers calcifiers resistance to ocean acidification. PMID:26778520

The Ice Cap Zone: A Unique Habitable Zone for Ocean Worlds

NASA Astrophysics Data System (ADS)

Ramirez, Ramses M.; Levi, Amit

2018-03-01

Traditional definitions of the habitable zone assume that habitable planets contain a carbonate-silicate cycle that regulates CO2 between the atmosphere, surface, and the interior. Such theories have been used to cast doubt on the habitability of ocean worlds. However, Levi et al (2017) have recently proposed a mechanism by which CO2 is mobilized between the atmosphere and the interior of an ocean world. At high enough CO2 pressures, sea ice can become enriched in CO2 clathrates and sink after a threshold density is achieved. The presence of subpolar sea ice is of great importance for habitability in ocean worlds. It may moderate the climate and is fundamental in current theories of life formation in diluted environments. Here, we model the Levi et al. mechanism and use latitudinally-dependent non-grey energy balance and single-column radiative-convective models and find that this mechanism may be sustained on ocean worlds that rotate at least 3 times faster than the Earth. We calculate the circumstellar region in which this cycle may operate for G-M-stars (Teff = 2,600-5,800 K), extending from ˜1.23 - 1.65, 0.69 - 0.873, 0.38-0.528 AU, 0.219-0.308 AU, 0.146-0.206 AU, and 0.0428-0.0617 AU for G2, K3, M0, M3, M5, and M8 stars, respectively. However, unless planets are very young and not tidally-locked, our mechanism would be unlikely to apply to stars cooler than a ˜M3. We predict C/O ratios for our atmospheres (˜0.5) that can be verified by the JWST mission.

The ice cap zone: a unique habitable zone for ocean worlds

NASA Astrophysics Data System (ADS)

Ramirez, Ramses M.; Levi, Amit

2018-07-01

Traditional definitions of the habitable zone assume that habitable planets contain a carbonate-silicate cycle that regulates CO2 between the atmosphere, surface, and the interior. Such theories have been used to cast doubt on the habitability of ocean worlds. However, Levi et al. have recently proposed a mechanism by which CO2 is mobilized between the atmosphere and the interior of an ocean world. At high enough CO2 pressures, sea ice can become enriched in CO2 clathrates and sink after a threshold density is achieved. The presence of subpolar sea ice is of great importance for habitability in ocean worlds. It may moderate the climate and is fundamental in current theories of life formation in diluted environments. Here, we model the Levi et al. mechanism and use latitudinally dependent non-grey energy balance and single-column radiative-convective climate models and find that this mechanism may be sustained on ocean worlds that rotate at least 3 times faster than the Earth. We calculate the circumstellar region in which this cycle may operate for G-M stars (Teff = 2600-5800 K), extending from ˜1.23-1.65, 0.69-0.954, 0.38-0.528, 0.219-0.308 , 0.146-0.206, and 0.0428-0.0617 au for G2, K2, M0, M3, M5, and M8 stars, respectively. However, unless planets are very young and not tidally locked, our mechanism would be unlikely to apply to stars cooler than a ˜M3. We predict C/O ratios for our atmospheres (˜0.5) that can be verified by the James Webb Space Telescope mission.

Atmosphere-ocean gas exchange based on radiocarbon data

NASA Astrophysics Data System (ADS)

Byalko, Alexey

2014-05-01

In recent decades, the intensity of global atmospheric convection has accelerated faster than climate warming; it is possible to judge this process from indirect data. Increasing ocean salinity contrasts provide evidence that evaporation has intensified [1]; sea surface wind velocities and wave heights have increased [2]. The CO2 gas exchange between the atmosphere and ocean must also simultaneously increase. Monthly measurements of atmospheric CO2 concentration have been published since 1958 [3], but directly measuring its fluxes from the atmosphere to the ocean and back is hardly possible. We show they can be reconstructed from 14C isotope concentration data. In the past century, two processes influenced the atmospheric 14C concentration in opposite directions: burning fossil fuels and testing nuclear weapons in the atmosphere. We compare the gas exchange theory with measurements of radiocarbon content in the atmosphere [4—6], which allows assessing the gas exchange quantitatively for the ocean to atmosphere and atmosphere to ocean fluxes separately for period 1960—2010 [7]. References 1. Durack P. J. and Wijffels S. E., J. Climate 23, 4342 (2010). 2. Young I. R., Sieger S., and Babanin A.V., Science 332, 451 (2011). 3. NOAA Earth System Research Laboratory Data: ftp://ftp.cmdl.noaa.gov/ccg/co2/trends/co2_mm_mlo.txt. 4. Nydal R., Lövseth K. // J. Geophys. Res. 1983. V. 88. P. 3579. 5. Levin I., Kromer B. // Radiocarbon. 1997. V. 39. P. 205. 6. Miller J.B., Lehman S.J., Montzka S.A., et al. // J. Geophys. Res. 2012. V. 117. D08302. 7. Byalko A.V. Doklady Physics, 2013. V. 58, 267-271.

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

NASA Astrophysics Data System (ADS)

Menviel, L.; Joos, F.

2012-03-01

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

Ocean acidification: Towards a better understanding of calcite dissolution

NASA Astrophysics Data System (ADS)

Wilhelmus, Monica M.; Adkins, Jess; Menemenlis, Dimitris

2016-11-01

The drastic increase of anthropogenic CO2 emissions over the past two centuries has altered the chemical structure of the ocean, acidifying upper ocean waters. The net impact of this pH decrease on marine ecosystems is still unclear, given the unprecedented rate at which CO2 is being released into the atmosphere. As part of the carbon cycle, calcium carbonate dissolution in sediments neutralizes CO2: phytoplankton at the surface produce carbonate minerals, which sink and reach the seafloor after the organisms die. On time scales of thousands of years, the calcium carbonate in these shells ultimately reacts with CO2 in seawater. Research in this field has been extensive; nevertheless, the dissolution rate law, the impact of boundary layer transport, and the feedback with the global ocean carbon cycle remain controversial. Here, we (i) develop a comprehensive numerical framework via 1D modeling of carbonate dissolution in sediments, (ii) approximate its impact on water column properties by implementing a polynomial approximation to the system's response into a global ocean biogeochemistry general circulation model (OBGCM), and (iii) examine the OBGCM sensitivity response to different formulations of sediment boundary layer properties. We find that, even though the burial equilibration time scales of calcium carbonate are in the order of thousands of years, the formulation of a bottom sediment model along with an improved description of the dissolution rate law can have consequences on multi-year to decadal time scales.

A seasonal carbon budget for a naturally iron-fertilized bloom over the Kerguelen Plateau in the Southern Ocean

NASA Astrophysics Data System (ADS)

Jouandet, Marie Paule; Blain, Stephane; Metzl, Nicolas; Brunet, Christian; Trull, Thomas W.; Obernosterer, Ingrid

2008-03-01

During the Kerguelen Ocean and Plateau compared Study (KEOPS, January-February 2005), a high-resolution distribution of surface fugacity of carbon dioxide ( fCO 2) was obtained from underway measurements. The stations in the core of the naturally iron-fertilized bloom were characterized by low fCO 2 (311±8 μatm) compared to the atmosphere, thus representing a large CO 2 sink. This contrasted with stations typical of high-nutrient low-chlorophyll (HNLC) conditions where the surface water was roughly in equilibrium with the atmosphere ( fCO 2=372±5 μatm). The vertical distribution of dissolved inorganic carbon (DIC) also was obtained at stations within and outside the bloom. Based on this data set, we constructed a carbon budget for the mixed layer that allowed us to determine the seasonal net community production (NCP season) and the seasonal carbon export in two contrasting environments. The robustness of the approach and the errors also were estimated. The NCP season in the core of the bloom was 6.6±2.2 mol m -2, typical of productive areas of the Southern Ocean. At the HNLC station the NCP season was 3 times lower than in the bloom. Our estimate of the daily net community production (NCP daily) within the bloom compares well with shipboard measurements of NCP. The NCP daily obtained above the Kerguelen Plateau was of the same order as the estimates from Southern Ocean artificial iron-fertilization experiments (SOIREE and EisenEx). The seasonal carbon export was derived from NCP season after subtraction of the seasonal accumulation of particulate and dissolved organic carbon. In the bloom, the carbon export (5.4±1.9 mol m -2) was 3-fold higher than at the HNLC station (1.7±0.4 mol m -2). Comparison of our results to artificial iron-fertilization experiments shows that the biological pump is enhanced by natural iron fertilization.

CO2 and circulation in the deglacial North Pacific

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Assessing ocean alkalinity for carbon sequestration

NASA Astrophysics Data System (ADS)

Renforth, Phil; Henderson, Gideon

2017-09-01

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

Mitigating Local Causes of Ocean Acidification with Existing Laws

EPA Science Inventory

The oceans continue to absorb CO2 in step with the increasing atmospheric concentration of CO2. The dissolved CO2 reacts with seawater to form carbonic acid (H2CO3) and liberate hydrogen ions, causing the pH of the oceans to decrease. Ocean acidification is thus an inevitable a...

Marine phytoplankton stoichiometry mediates nonlinear interactions between nutrient supply, temperature, and atmospheric CO2

NASA Astrophysics Data System (ADS)

Moreno, Allison R.; Hagstrom, George I.; Primeau, Francois W.; Levin, Simon A.; Martiny, Adam C.

2018-05-01

Marine phytoplankton stoichiometry links nutrient supply to marine carbon export. Deviations of phytoplankton stoichiometry from Redfield proportions (106C : 1P) could therefore have a significant impact on carbon cycling, and understanding which environmental factors drive these deviations may reveal new mechanisms regulating the carbon cycle. To explore the links between environmental conditions, stoichiometry, and carbon cycling, we compared four different models of phytoplankton C : P: a fixed Redfield model, a model with C : P given as a function of surface phosphorus concentration (P), a model with C P given as a function of temperature, and a new multi-environmental model that predicts C : P as a function of light, temperature, and P. These stoichiometric models were embedded into a five-box ocean circulation model, which resolves the three major ocean biomes (high-latitude, subtropical gyres, and tropical upwelling regions). Contrary to the expectation of a monotonic relationship between surface nutrient drawdown and carbon export, we found that lateral nutrient transport from lower C : P tropical waters to high C : P subtropical waters could cause carbon export to decrease with increased tropical nutrient utilization. It has been hypothesized that a positive feedback between temperature and pCO2, atm will play an important role in anthropogenic climate change, with changes in the biological pump playing at most a secondary role. Here we show that environmentally driven shifts in stoichiometry make the biological pump more influential, and may reverse the expected positive relationship between temperature and pCO2, atm. In the temperature-only model, changes in tropical temperature have more impact on the Δ pCO2, atm (˜ 41 ppm) compared to subtropical temperature changes (˜ 4.5 ppm). Our multi-environmental model predicted a decline in pCO2, atm of ˜ 46 ppm when temperature spanned a change of 10 °C. Thus, we find that variation in marine phytoplankton stoichiometry and its environmental controlling factors can lead to nonlinear controls on pCO2, atm, suggesting the need for further studies of ocean C : P and the impact on ocean carbon cycling.

Enhanced chemical weathering as a geoengineering strategy to reduce atmospheric carbon dioxide, supply nutrients, and mitigate ocean acidification

NASA Astrophysics Data System (ADS)

Hartmann, Jens; West, A. Joshua; Renforth, Phil; Köhler, Peter; De La Rocha, Christina L.; Wolf-Gladrow, Dieter A.; Dürr, Hans H.; Scheffran, Jürgen

2013-04-01

weathering is an integral part of both the rock and carbon cycles and is being affected by changes in land use, particularly as a result of agricultural practices such as tilling, mineral fertilization, or liming to adjust soil pH. These human activities have already altered the terrestrial chemical cycles and land-ocean flux of major elements, although the extent remains difficult to quantify. When deployed on a grand scale, Enhanced Weathering (a form of mineral fertilization), the application of finely ground minerals over the land surface, could be used to remove CO2 from the atmosphere. The release of cations during the dissolution of such silicate minerals would convert dissolved CO2 to bicarbonate, increasing the alkalinity and pH of natural waters. Some products of mineral dissolution would precipitate in soils or be taken up by ecosystems, but a significant portion would be transported to the coastal zone and the open ocean, where the increase in alkalinity would partially counteract "ocean acidification" associated with the current marked increase in atmospheric CO2. Other elements released during this mineral dissolution, like Si, P, or K, could stimulate biological productivity, further helping to remove CO2 from the atmosphere. On land, the terrestrial carbon pool would likely increase in response to Enhanced Weathering in areas where ecosystem growth rates are currently limited by one of the nutrients that would be released during mineral dissolution. In the ocean, the biological carbon pumps (which export organic matter and CaCO3 to the deep ocean) may be altered by the resulting influx of nutrients and alkalinity to the ocean. This review merges current interdisciplinary knowledge about Enhanced Weathering, the processes involved, and the applicability as well as some of the consequences and risks of applying the method.

The Global Ocean Observing System

NASA Technical Reports Server (NTRS)

Kester, Dana

1992-01-01

A Global Ocean Observing System (GOOS) should be established now with international coordination (1) to address issues of global change, (2) to implement operational ENSO forecasts, (3) to provide the data required to apply global ocean circulation models, and (4) to extract the greatest value from the one billion dollar investment over the next ten years in ocean remote sensing by the world's space agencies. The objectives of GOOS will focus on climatic and oceanic predictions, on assessing coastal pollution, and in determining the sustainability of living marine resources and ecosystems. GOOS will be a complete system including satellite observations, in situ observations, numerical modeling of ocean processes, and data exchange and management. A series of practical and economic benefits will be derived from the information generated by GOOS. In addition to the marine science community, these benefits will be realized by the energy industries of the world, and by the world's fisheries. The basic oceanic variables that are required to meet the oceanic and predictability objectives of GOOS include wind velocity over the ocean, sea surface temperature and salinity, oceanic profiles of temperature and salinity, surface current, sea level, the extent and thickness of sea ice, the partial pressure of CO2 in surface waters, and the chlorophyll concentration of surface waters. Ocean circulation models and coupled ocean-atmosphere models can be used to evaluate observing system design, to assimilate diverse data sets from in situ and remotely sensed observations, and ultimately to predict future states of the system. The volume of ocean data will increase enormously over the next decade as new satellite systems are launched and as complementary in situ measuring systems are deployed. These data must be transmitted, quality controlled, exchanged, analyzed, and archived with the best state-of-the-art computational methods.

Do Southern Ocean Cloud Feedbacks Matter for 21st Century Warming?

NASA Astrophysics Data System (ADS)

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

2017-12-01

Cloud phase improvements in a state-of-the-art climate model produce a large 1.5 K increase in equilibrium climate sensitivity (ECS, the surface warming in response to instantaneously doubled CO2) via extratropical shortwave cloud feedbacks. Here we show that the same model improvements produce only a small surface warming increase in a realistic 21st century emissions scenario. The small 21st century warming increase is attributed to extratropical ocean heat uptake. Southern Ocean mean-state circulation takes up heat while a slowdown in North Atlantic circulation acts as a feedback to slow surface warming. Persistent heat uptake by extratropical oceans implies that extratropical cloud biases may not be as important to 21st century warming as biases in other regions. Observational constraints on cloud phase and shortwave radiation that produce a large ECS increase do not imply large changes in 21st century warming.

Evidence for ocean acidification in the Great Barrier Reef of Australia

NASA Astrophysics Data System (ADS)

Wei, Gangjian; McCulloch, Malcolm T.; Mortimer, Graham; Deng, Wengfeng; Xie, Luhua

2009-04-01

Geochemical records preserved in the long-lived carbonate skeleton of corals provide one of the few means to reconstruct changes in seawater pH since the commencement of the industrial era. This information is important in not only determining the response of the surface oceans to ocean acidification from enhanced uptake of CO 2, but also to better understand the effects of ocean acidification on carbonate secreting organisms such as corals, whose ability to calcify is highly pH dependent. Here we report an ˜200 year δ 11B isotopic record, extracted from a long-lived Porites coral from the central Great Barrier Reef of Australia. This record covering the period from 1800 to 2004 was sampled at yearly increments from 1940 to the present and 5-year increments prior to 1940. The δ 11B isotopic compositions reflect variations in seawater pH, and the δ 13C changes in the carbon composition of surface water due to fossil fuel burning over this period. In addition complementary Ba/Ca, δ 18O and Mg/Ca data was obtained providing proxies for terrestrial runoff, salinity and temperature changes over the past 200 years in this region. Positive thermal ionization mass spectrometry (PTIMS) method was utilized in order to enable the highest precision and most accurate measurements of δ 11B values. The internal precision and reproducibility for δ 11B of our measurements are better than ±0.2‰ (2 σ), which translates to a precision of better than ±0.02 pH units. Our results indicate that the long-term pre-industrial variation of seawater pH in this region is partially related to the decadal-interdecadal variability of atmospheric and oceanic anomalies in the Pacific. In the periods around 1940 and 1998 there are also rapid oscillations in δ 11B compositions equivalent changes in pH of almost 0.5 U. The 1998 oscillation is co-incident with a major coral bleaching event indicating the sensitivity of skeletal δ 11B compositions to loss of zooxanthellate symbionts. Importantly, from the 1940s to the present-day, there is a general overall trend of ocean acidification with pH decreasing by about 0.2-0.3 U, the range being dependent on the value assumed for the fractionation factor α(B3-B4) of the boric acid and borate species in seawater. Correlations of δ 11B with δ 13C during this interval indicate that the increasing trend towards ocean acidification over the past 60 years in this region is the result of enhanced dissolution of CO 2 in surface waters from the rapidly increasing levels of atmospheric CO 2, mainly from fossil fuel burning. This suggests that the increased levels of anthropogenic CO 2 in atmosphere has already caused a significant trend towards acidification in the oceans during the past decades. Observations of surprisingly large decreases in pH across important carbonate producing regions, such as the Great Barrier Reef of Australia, raise serious concerns about the impact of Greenhouse gas emissions on coral calcification.

Carbon Cycling and pH regulation on the Scotian Shelf, NW Atlantic

NASA Astrophysics Data System (ADS)

Thomas, Helmuth

2015-04-01

This presentation intends to describe the biogeochemical context for ocean acidification studies on the Scotian Shelf. The seasonality of the dominant processes, regulating surface ocean CO2 conditions, including pH, will be assessed as well as cross-shelf transports of CO2, acidity and nutrient, the latter ones exerting the "subsurface control" of CO2 air-sea fluxes and surface pH. Methods summary: The seasonal variability of inorganic carbon in the surface waters of the Scotian Shelf region of the Canadian northwestern Atlantic Ocean was assessed using hourly measurements of the partial pressure of CO2 (pCO2), and hydrographic variables obtained by an autonomous moored instrument (44.3°N and 63.3°W). These measurements were complemented by seasonal shipboard sampling of dissolved inorganic carbon (DIC), total alkalinity (TA), and pCO2, at the mooring site, and over the larger spatial scale. The Scotian Shelf is a 700 km long section of the continental shelf off Nova Scotia. Bounded by the Laurentian Channel to the northeast, and by the Northeast Channel and the Gulf of Maine to the southwest, it varies in width from 120 to 240 km covering roughly 120,000 km2 with an average depth of 90 m . Convective mixin in winter time and coastal upwelling and the associated favorable wind conditions on the Scotian Shelf have long been recognized. Strong winds of speeds greater than 10 m s-1, blowing to the northeast, and persisting for several days force relatively cold, saline, water toward the surface, displacing the warmer, fresher water offshore. Upwelling events have frequently been observed in the region in winter, and modeling studies have reproduced these observed events. Furthermore, these events may play a role in initiating and sustaining the spring phytoplankton bloom by displacing nutrient-depleted surface water and bring nutrient-rich waters up to the surface. Biological processes were found to be the dominant control on mixed-layer DIC, with the delivery of carbon-rich subsurface waters also playing an important role. The region acts as a net source of CO2 to the atmosphere at the annual scale, with a reversal of this trend occurring only during the diatom dominated spring phytoplankton bloom, when a pronounced undersaturation of the surface waters is reached for a short period. During that time, the pH is at its annual maximum (pH≈8.15), while the Aragonite saturation state reaches its minimum just before the onset of the spring bloom in late March. After of the spring bloom period, the competing effects of temperature and biology influence surface pCO2 in roughly equal magnitude. During that time carbon fixation is driven by the smaller phytoplankton size classes, which can grow in warmer, nutrient poor conditions. In the Scotian Shelf region the summertime population these numerically abundant small cells accounts for approximately 10-20% of annual carbon uptake. The regional mean surface water pH is roughly 7.8 in April and increases to greater than 8.0 in September; subsurface pH is approximately 7.6 throughout the region and indicates a seasonal decrease due to the respiration of organic matter at depth. The surface aragonite saturation state increases from less than 2.0 to values as high as 3.2 between April and September; the region as a whole exhibits relatively low saturation states, however values approaching 1.0 were only observed in the Cabot Strait at depths below roughly 100m. Subsurface onshore gradients of CO2 and nutrient species yield onshore carbon, nutrient and hydrogen ion (H+) fluxes in subsurface waters, which in turn regulate surface pH and fuel the CO2 outgassing from the Scotian Shelf.

Ocean acidification reduces transfer of essential biomolecules in a natural plankton community

PubMed Central

Bermúdez, J. Rafael; Riebesell, Ulf; Larsen, Aud; Winder, Monika

2016-01-01

Ocean acidification (OA), a process of increasing seawater acidity caused by the uptake of anthropogenic carbon dioxide (CO2) by the ocean, is expected to change surface ocean pH to levels unprecedented for millions of years, affecting marine food web structures and trophic interactions. Using an in situ mesocosm approach we investigated effects of OA on community composition and trophic transfer of essential fatty acids (FA) in a natural plankton assemblage. Elevated pCO2 favored the smallest phytoplankton size class in terms of biomass, primarily picoeukaryotes, at the expense of chlorophyta and haptophyta in the nano-plankton size range. This shift in community composition and size structure was accompanied by a decline in the proportion of polyunsaturated FA (PUFA) to total FA content in the nano- and picophytoplankton size fractions. This decline was mirrored in a continuing reduction in the relative PUFA content of the dominant copepod, Calanus finmarchicus, which primarily fed on the nano-size class. Our results demonstrate that a shift in phytoplankton community composition and biochemical composition in response to rising CO2 can affect the transfer of essential compounds to higher trophic levels, which rely on their prey as a source for essential macromolecules. PMID:27324057

Strengthening seasonal marine CO2 variations due to increasing atmospheric CO2

NASA Astrophysics Data System (ADS)

Landschützer, Peter; Gruber, Nicolas; Bakker, Dorothee C. E.; Stemmler, Irene; Six, Katharina D.

2018-01-01

The increase of atmospheric CO2 (ref. 1) has been predicted to impact the seasonal cycle of inorganic carbon in the global ocean2,3, yet the observational evidence to verify this prediction has been missing. Here, using an observation-based product of the oceanic partial pressure of CO2 (pCO2) covering the past 34 years, we find that the winter-to-summer difference of the pCO2 has increased on average by 2.2 ± 0.4 μatm per decade from 1982 to 2015 poleward of 10° latitude. This is largely in agreement with the trend expected from thermodynamic considerations. Most of the increase stems from the seasonality of the drivers acting on an increasing oceanic pCO2 caused by the uptake of anthropogenic CO2 from the atmosphere. In the high latitudes, the concurrent ocean-acidification-induced changes in the buffer capacity of the ocean enhance this effect. This strengthening of the seasonal winter-to-summer difference pushes the global ocean towards critical thresholds earlier, inducing stress to ocean ecosystems and fisheries4. Our study provides observational evidence for this strengthening seasonal difference in the oceanic carbon cycle on a global scale, illustrating the inevitable consequences of anthropogenic CO2 emissions.

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

NASA Astrophysics Data System (ADS)

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

2018-04-01

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

Enhanced transfer of organic matter to higher trophic levels caused by ocean acidification and its implications for export production: A mass balance approach

PubMed Central

Taucher, Jan; Bach, Lennart T.; Achterberg, Eric P.; Algueró-Muñiz, María; Bellworthy, Jessica; Czerny, Jan; Esposito, Mario; Haunost, Mathias; Hellemann, Dana; Ludwig, Andrea; Yong, Jaw C.; Zark, Maren; Riebesell, Ulf; Anderson, Leif G.

2018-01-01

Ongoing acidification of the ocean through uptake of anthropogenic CO2 is known to affect marine biota and ecosystems with largely unknown consequences for marine food webs. Changes in food web structure have the potential to alter trophic transfer, partitioning, and biogeochemical cycling of elements in the ocean. Here we investigated the impact of realistic end-of-the-century CO2 concentrations on the development and partitioning of the carbon, nitrogen, phosphorus, and silica pools in a coastal pelagic ecosystem (Gullmar Fjord, Sweden). We covered the entire winter-to-summer plankton succession (100 days) in two sets of five pelagic mesocosms, with one set being CO2 enriched (~760 μatm pCO2) and the other one left at ambient CO2 concentrations. Elemental mass balances were calculated and we highlight important challenges and uncertainties we have faced in the closed mesocosm system. Our key observations under high CO2 were: (1) A significantly amplified transfer of carbon, nitrogen, and phosphorus from primary producers to higher trophic levels, during times of regenerated primary production. (2) A prolonged retention of all three elements in the pelagic food web that significantly reduced nitrogen and phosphorus sedimentation by about 11 and 9%, respectively. (3) A positive trend in carbon fixation (relative to nitrogen) that appeared in the particulate matter pool as well as the downward particle flux. This excess carbon counteracted a potential reduction in carbon sedimentation that could have been expected from patterns of nitrogen and phosphorus fluxes. Our findings highlight the potential for ocean acidification to alter partitioning and cycling of carbon and nutrients in the surface ocean but also show that impacts are temporarily variable and likely depending upon the structure of the plankton food web. PMID:29799856

NASA's Carbon Monitoring System Flux-Pilot Project: A Multi-Component Analysis System for Carbon-Cycle Research and Monitoring

NASA Technical Reports Server (NTRS)

Pawson, S.; Gunson, M.; Potter, C.; Jucks, K.

2012-01-01

The importance of greenhouse gas increases for climate motivates NASA s observing strategy for CO2 from space, including the forthcoming Orbiting Carbon Observatory (OCO-2) mission. Carbon cycle monitoring, including attribution of atmospheric concentrations to regional emissions and uptake, requires a robust modeling and analysis infrastructure to optimally extract information from the observations. NASA's Carbon-Monitoring System Flux-Pilot Project (FPP) is a prototype for such analysis, combining a set of unique tools to facilitate analysis of atmospheric CO2 along with fluxes between the atmosphere and the terrestrial biosphere or ocean. NASA's analysis system is unique, in that it combines information and expertise from the land, oceanic, and atmospheric branches of the carbon cycle and includes some estimates of uncertainty. Numerous existing space-based missions provide information of relevance to the carbon cycle. This study describes the components of the FPP framework, assessing the realism of computed fluxes, thus providing the basis for research and monitoring applications. Fluxes are computed using data-constrained terrestrial biosphere models and physical ocean models, driven by atmospheric observations and assimilating ocean-color information. Use of two estimates provides a measure of uncertainty in the fluxes. Along with inventories of other emissions, these data-derived fluxes are used in transport models to assess their consistency with atmospheric CO2 observations. Closure is achieved by using a four-dimensional data assimilation (inverse) approach that adjusts the terrestrial biosphere fluxes to make them consistent with the atmospheric CO2 observations. Results will be shown, illustrating the year-to-year variations in land biospheric and oceanic fluxes computed in the FPP. The signals of these surface-flux variations on atmospheric CO2 will be isolated using forward modeling tools, which also incorporate estimates of transport error. The results will be discussed in the context of interannual variability of observed atmospheric CO2 distributions.

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

NASA Astrophysics Data System (ADS)

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

2014-12-01

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

Oceanic ecosystem dynamics during gigantic volcanic episodes: the Ontong Java and Manihiki Plateaus recorded by calcareous nannoplankton. (Invited)

NASA Astrophysics Data System (ADS)

Erba, E.

2010-12-01

Earth's volcanic activity introduces environmental stress that biota are forced to survive. There is a general consensus on the role of volcanogenic carbon dioxide increases, and implicit tectonic-igneous events, triggering major climate changes and profound variations in chemical, physical and trophic characteristics of the oceans through the Phanerozoic. Cretaceous geological records indicate conditions of excess atmCO2 (up to 2000-3000 ppm) derived from construction of Large Igneous Provinces (LIPs). In such “high CO2 world” and greenhouse conditions, the deep ocean became depleted of oxygen promoting the accumulation and burial of massive amounts of organic matter; such episodes are recognized as Oceanic Anoxic Events (OAEs) and their geological records merit careful examination of how the Earth system, and Life in particular, can overcome extreme experiments of global change. The Early Aptian (˜ 120 million years ago) OAE1a is a complex example of volcanicCO2-induced environmental stress. There is a general consensus on the causes of this case-history, namely excess CO2 derived from the construction of the Ontong Java-Manihiki LIP. Multi- and inter-disciplinary studies of the OAE1a have pointed out C, O, Os, Sr isotopic anomalies, a biocalcification crisis in pelagic and neritic settings, enhanced fertility and primary productivity, as well as ocean acidification. Available cyclochronology allows high-resolution dating of biotic and environmental fluctuations, providing the precision necessary for understanding the role of volcanogenic CO2 on nannoplankton biocalcification, adaptations, evolutionary innovation and/or extinctions. The reconstructed sequence of volcanogenic CO2 pulses, and perhaps some clathrate melting, triggered a climate change to supergreenhouse conditions, anoxia and ocean acidification. The demise of heavily calcified nannoconids and reduced calcite paleofluxes marks beginning of the pre-OAE1a calcification crisis. Ephemeral coccolith dwarfism and malformation represent adjustments to survive lower pH. Deep-water acidification occurs with a delay of 25-30 thousand years: a dissolution event recording 1 to 2km shallowing of the Calcite Compensation Depth anticipated the onset of anoxic sedimentation. A major acceleration in weathering has been identified in the lowermost part of OAE1a. After acidification-dissolution climax, nannoplankton and carbonate recovery developed over ~160 kyr, under persisting global dysoxia-anoxia. This recovery presumably implies a stasis of the LIP activity and gradual buffering of ocean acidification or a decrease in volcanogenic CO2 emissions and consistently higher CO2 drawdown through Corg burial and/or weathering. Rising CO2 and surface-ocean acidification during OAE1a triggered false extinctions among calcareous nannoplankton. Conversely, a major origination episode starts approximately 1 My before global anoxia and persists through OAE1a and associated acidification. Increasing pCO2 caused complex and species-specific reactions, including production of r-strategist taxa, which, however, secreted dwarf and malformed coccoliths as a strategy to overcome acidification.

Impact of anthropogenic CO2 on the CaCO3 system in the oceans.

PubMed

Feely, Richard A; Sabine, Christopher L; Lee, Kitack; Berelson, Will; Kleypas, Joanie; Fabry, Victoria J; Millero, Frank J

2004-07-16

Rising atmospheric carbon dioxide (CO2) concentrations over the past two centuries have led to greater CO2 uptake by the oceans. This acidification process has changed the saturation state of the oceans with respect to calcium carbonate (CaCO3) particles. Here we estimate the in situ CaCO3 dissolution rates for the global oceans from total alkalinity and chlorofluorocarbon data, and we also discuss the future impacts of anthropogenic CO2 on CaCO3 shell-forming species. CaCO3 dissolution rates, ranging from 0.003 to 1.2 micromoles per kilogram per year, are observed beginning near the aragonite saturation horizon. The total water column CaCO3 dissolution rate for the global oceans is approximately 0.5 +/- 0.2 petagrams of CaCO3-C per year, which is approximately 45 to 65% of the export production of CaCO3.

Maximum Drawdown of Atmospheric CO2 due to Biological Uptake in the Ocean and the Ocean Temperature Effect

NASA Astrophysics Data System (ADS)

Odalen, M.; Nycander, J.; Oliver, K. I. C.; Nilsson, J.; Brodeau, L.; Ridgwell, A.

2016-02-01

During glacials, atmospheric CO2 is significantly lowered; the decrease is about 1/3 or 90 ppm during the last four glacial cycles. Since the ocean reservoir of carbon, and hence the ocean capacity for storing carbon, is substantially larger than the atmospheric and terrestrial counterparts, it is likely that this lowering was caused by ocean processes, drawing the CO2 into the deep ocean. The Southern Ocean circulation and biological efficiency are widely accepted as having played an important part in this CO2 drawdown. However, the relative effects of different processes contributing to this oceanic uptake have not yet been well constrained. In this work, we focus on better constraining two of these processes; 1) the effect of increased efficiency of the biological carbon uptake, and 2) the effect of changes in global mean ocean temperature on the abiotic ocean-atmosphere CO2 equilibrium. By performing ensemble runs using an Earth System Model of Intermediate Complexity (EMIC) we examine the changes in atmospheric pCO2 achieved by 100% nutrient utilization efficiency of biology. The simulations display different ocean circulation patterns and hence different global ocean mean temperatures. By restoring the atmospheric pCO2 to a target value during the spin-up phase, the total carbon content differs between each of the ensemble members. The difference is due to circulation having direct effects on biology, but also on global ocean mean temperature, changing the solubility of CO2. This study reveals the relative importance of of the processes 1 and 2 (mentioned above) for atmospheric pCO2 in a changed climate. The results of this study also show that a difference in carbon content after spin-up can have a significant effect on the drawdown potential of a maximised biological efficiency. Thus, the choice of spin-up characteristics in a model study of climate change CO2 dynamics may significantly affect the outcome of the study.

Are Salps A Silver Bullet Against Global Warming And Ocean Acidification?

NASA Astrophysics Data System (ADS)

Kithil, P. W.

2006-12-01

Oceanic uptake of 25 billion tons CO2 annually introduced into the atmosphere from carbon fuels must be mitigated to prevent further widespread changes in ocean biochemistry and potentially severe anthropogenic climate change. Larry Madin of Woods Hole Oceanographic Institute and his colleagues have measured the carbon sequestration in the excretia produced by dense swarms of Salps of up to 4,000 tons per day over a 100,000 km2 ocean region, equivalent to over 14 thousand tons of CO2 per day. This poses several questions: 1. Given the ocean surface of 372 million km2, does the Madin report imply a potential removal of 20 billion tons of CO2 per year 80% of emissions? 2. What might be the natural limitations on widespread propagation of Salps, and how would these effect the carbon sequestration actually achieved? 3. What mechanism could encourage the propagation of Salps throughout the oceans? Since Salps feast on phytoplankton which require sunlight and sufficient nutrients, we must first reduce the available ocean by perhaps 60% as a seasonal limit on phytoplankton growth and allow 60% further limit for poor nutrient availability and assuming some ocean regions are an unfavorable environment for Salps. Combined, the net ocean area over which Salps could sequester carbon is thus 36%, or 134 million km2. Assuming Madin's values for carbon sequestration are achievable over this ocean region, about 7.2 billion tons of CO2 could be sequestered annually, equal to 29% of mankind's current fossil-fuel CO2 output. This converts to a carbon equivalent of 1.96 billion tons per year. The mechanism we propose to encourage widespread propagation of Salps is forced upwelling using Atmocean's arrays of wave-driven deep ocean pumps to bring up large volumes of cold, nutrient-rich deep ocean to enhance the ocean's primary production, absorbing CO2 and producing oxygen. The pump simply comprises a buoy, flexible tube, cylinder with valve, cable to connect the buoy and cylinder, and solar panel to power communications & provide remote control. Adjacent pumps are connected at the bottom to maintain relative position. If required, periodic seafloor anchoring can maintain absolute position within an ocean basin. Deployment is low cost as the pumps self-deploy when dropped into the ocean from barges. Pumps would not be deployed in ocean shipping channels, regions used by recreational boaters, nor where excessive tides or currents exist. In a global application, 1,340 arrays each 100,000 km2 are needed to cover the 134 million km2 calculated above. Assuming one pump per square km costing 2,000, an investment of 268 billion is needed. Using a five year payback, this investment is recouped if the carbon credit price is 26.80 per ton applied to sequestering 1.96 billion tons per year of carbon. This is not dramatically different from today's carbon credit price of about 15 per ton. Assuming a governmental mandate of carbon sequestration, today's price could easily increase many-fold, making ocean sequestration using forced upwelling economically attractive. Additional benefits of widespread forced upwelling include: 1 Buffering of ocean pH by removing CO2 during photosynthesis; 2 Possible cooling the upper mixed layer upstream from coral reefs to reduce bleaching from ocean hotspots; 3 Possible mitigation of rapid climate change by enhancing the mixing of arctic/Greenland meltwater; 4 Enhancement of wild fish populations; and, 5 Reduced hurricane intensity, achieved by cooling the upper mixed layer upon approach of a tropical storm in high risk regions such as the Gulf of Mexico.

From up to date climate and ocean evidence with updated UN emissions projections, the time is now to recommend an immediate massive effort on CO2.

NASA Astrophysics Data System (ADS)

Carter, Peter

2017-04-01

This paper provides further compelling evidence for 'an immediate, massive effort to control CO2 emissions, stopped by mid-century' (Cai, Lenton & Lontzek, 2016). Atmospheric CO2 which is above 405 ppm (actual and trend) still accelerating, despite flat emissions since 2014, with a 2015 >3ppm unprecedented spike in Earth history (A. Glikson),is on the worst case IPCC scenario. Atmospheric methane is increasing faster than its past 20-year rate, almost on the worst-case IPCC AR5 scenario (Global Carbon Project, 2016). Observed effects of atmospheric greenhouse gas (GHG) pollution are increasing faster. This includes long-lived atmospheric GHG concentrations, radiative forcing, surface average warming, Greenland ice sheet melting, Arctic daily sea ice anomaly, ocean heat (and rate of going deeper), ocean acidification, and ocean de-oxygenation. The atmospheric GHG concentration of 485 ppm CO2 eq (WMO, 2015) commits us to 'about 2°C' equilibrium (AR5). 2°C by 2100 would require 'substantial emissions reductions over the next few decades' (AR5). Instead, the May 2016 UN update on 'intended' national emissions targets under the Paris Agreement projects global emissions will be 16% higher by 2030 and the November 2016 International Energy Agency update projects energy-related CO2 eq emissions will be 30% higher by 2030, leading to 'around 2.7°C by 2100 and above 3°C thereafter'. Climate change feedback will be positive this century and multiple large vulnerable sources of amplifying feedback exist (AR5). 'Extensive tree mortality and widespread forest die-back linked to drought and temperature stress have been documented on all vegetated continents' (AR5). 'Recent studies suggest a weakening of the land sink, further amplifying atmospheric growth of CO2' (WMO, 2016). Under all but the best-case IPCC AR5 scenario, surface temperature is projected to increase above 2°C by 2100, which is above 3°C (equilibrium) after 2100, with ocean acidification still increasing at 2100. Ocean heat is increasing under all scenarios at 2100. For all producing regions 'With or without adaptation, negative impacts on average crop yields become likely from the 2030s' (AR5). Crop models do not capture all adverse effects. The climate change of 2030 is practically locked in. NASA NEX downscaled daily maximum temperature projections at 1.5°C are incompatible with today's crop yields in major agricultural regions. Climate-change-related impacts from extreme events are high at 1.5°C (AR5) and add to modeled crop declines. 'Some unique and threatened systems are already at risk from climate change (high confidence)' with 'risk of severe consequences' higher with warming of around 1.5°C (AR5). At today's surface temperature increase, 'risks associated with tipping points become moderate' and 'increase disproportionately' as temperature increases above 1.5°C (AR5). According to mitigation projections, global emissions would decline forthwith for a better than 66% chance of a 2°C limit by 2100 (over 3°C after 2100). Failure to do so would risk the future sustainability of civilization and the human population. The IPCC does not make recommendations so this falls on scientists. By recommending immediate (emergency) massive action on CO2, the science community would make a momentous contribution to the future of humanity.

On the relationships of gas transfer velocity with turbulent kinetic energy dissipation rate and wind waves

NASA Astrophysics Data System (ADS)

Zhao, D.

2012-12-01

The exchange of carbon dioxide across the air-sea interface is an important component of the atmospheric CO2 budget. Understanding how future changes in climate will affect oceanic uptake and releaser CO2 requires accurate estimation of air-sea CO2 flux. This flux is typically expressed as the product of gas transfer velocity, CO2 partial pressure difference in seawater and air, and the CO2 solubility. As the key parameter, gas transfer velocity has long been known to be controlled by the near-surface turbulence in water, which is affected by many factors, such as wind forcing, ocean waves, water-side convection and rainfall. Although the wind forcing is believed as the major factor dominating the near-surface turbulence, many studies have shown that the wind waves and their breaking would greatly enhance turbulence compared with the classical solid wall theory. Gas transfer velocity has been parameterized in terms of wind speed, turbulent kinetic energy dissipation rate, and wave parameters on the basis of observational data or theoretical analysis. However, great discrepancies, as large as one order, exist among these formulas. In this study, we will systematically analyze the differences of gas transfer velocity proposed so far, and try to find the reason that leads to their uncertainties. Finally, a new formula for gas transfer velocity will be given in terms of wind speed and wind wave parameter.

Temporal Variability of North Atlantic Carbon Fluxes and their Sensitivity to the Meridional Overturning Circulation

NASA Astrophysics Data System (ADS)

Brown, P.; McDonagh, E.; Sanders, R.; King, B.; Watson, A. J.; Schuster, U.; Henson, S.

2016-02-01

The North Atlantic plays a critical role in the global carbon cycle both as a region of substantial air-sea carbon dioxide uptake and as a location for the transfer of CO2 to depth on climatically-important timescales. While the magnitude of surface fluxes is relatively well constrained, our understanding of the processes that drive variability in ocean-atmosphere exchange and subsequent subsurface carbon accumulation is not as well defined. Here we present observation-derived high-resolution estimates of short-term 10-day meridional ocean carbon transport variability across the subtropical North Atlantic for 2004-2012. Substantial seasonal, sub-annual and interannual transport variability is observed that is highly sensitive to the strength of the Atlantic Meridional Overturning Circulation. While the recently identified multi-year decrease in AMOC strength similarly impacts carbon transports, its full effect is masked by the northwards transport of increasing surface CO2 levels. A 30% slowdown in the meridional circulation in 2009-2010 and the anomalous effects it had on the transport, storage and divergence of heat and freshwater in the subtropical and subpolar gyres and local wind regimes are investigated for their impact on local air-sea CO2 fluxes. Temperature and salt content anomalies identified in each gyre are found to drive (subtropics) or hinder (subpolar) additional carbon uptake from the atmosphere by affecting the physical solubility pump for CO2. Additionally their simultaneous effect on mixed layer depth and the vertical supply of nutrients to the surface is shown to magnify the CO2 flux observed by driving anomalous primary production rates.

Evaluation of NASA's Carbon Monitoring System (CMS) Flux Pilot: Terrestrial CO2 Fluxes

NASA Astrophysics Data System (ADS)

Fisher, J. B.; Polhamus, A.; Bowman, K. W.; Collatz, G. J.; Potter, C. S.; Lee, M.; Liu, J.; Jung, M.; Reichstein, M.

2011-12-01

NASA's Carbon Monitoring System (CMS) flux pilot project combines NASA's Earth System models in land, ocean and atmosphere to track surface CO2 fluxes. The system is constrained by atmospheric measurements of XCO2 from the Japanese GOSAT satellite, giving a "big picture" view of total CO2 in Earth's atmosphere. Combining two land models (CASA-Ames and CASA-GFED), two ocean models (ECCO2 and NOBM) and two atmospheric chemistry and inversion models (GEOS-5 and GEOS-Chem), the system brings together the stand-alone component models of the Earth System, all of which are run diagnostically constrained by a multitude of other remotely sensed data. Here, we evaluate the biospheric land surface CO2 fluxes (i.e., net ecosystem exchange, NEE) as estimated from the atmospheric flux inversion. We compare against the prior bottom-up estimates (e.g., the CASA models) as well. Our evaluation dataset is the independently derived global wall-to-wall MPI-BGC product, which uses a machine learning algorithm and model tree ensemble to "scale-up" a network of in situ CO2 flux measurements from 253 globally-distributed sites in the FLUXNET network. The measurements are based on the eddy covariance method, which uses observations of co-varying fluxes of CO2 (and water and energy) from instruments on towers extending above ecosystem canopies; the towers integrate fluxes over large spatial areas (~1 km2). We present global maps of CO2 fluxes and differences between products, summaries of fluxes by TRANSCOM region, country, latitude, and biome type, and assess the time series, including timing of minimum and maximum fluxes. This evaluation shows both where the CMS is performing well, and where improvements should be directed in further work.

Foraminifer Shell Weight and Fragmentation: A Quantitative Study of the Influence of Temperature, [CO32-] and Dissolution on Proxies of the Marine Carbonate System

NASA Astrophysics Data System (ADS)

Mekik, F.; Pourmand, A.; Ward, B. M.

2015-12-01

Quantifying the various components of the marine carbonate system is important for understanding anthropogenic ocean acidification, and the rates and magnitudes of ocean acidification/ alkalization events in Earth's past. We performed multiple statistical analyses (factor analysis, partial correlations, multiple regression analysis and independent samples t -tests) on core top data using the Globorotalia menardii fragmentation index (MFI) in 89 core tops from across the tropical Pacific, Atlantic and Indian Oceans, the fragmentation trend of four species of foraminifers (Globorotalia truncatulinoides, G. menardii, Neogloboquadrina dutertrei and Pulleniatina obliquiloculata) in the EEP, tropical Atlantic and tropical Indian Ocean core tops, and Globorotalia menardii shell weight in a suite of 25 core tops the EEP in order to isolate the effects of surface ocean parameters such as temperature and [CO32-] from dissolution in sediments. Surface ocean parameters showed no significant effect on the G. menardii fragmentation index. We found no statistically significant influence of habitat water temperature or [CO32-] on foraminifer fragmentation in any of four species. While we found a strong influence of habitat water [CO32-] on the size normalized shell weight proxy in N. dutertrei and Pulleniatina obliquiloculata in our previous work, we found a much reduced influence of [CO32-] on the shell weight of G. menardii, which is most influenced by shell dissolution.

Decadal changes in the aragonite and calcite saturation state of the Pacific Ocean

NASA Astrophysics Data System (ADS)

Feely, Richard A.; Sabine, Christopher L.; Byrne, Robert H.; Millero, Frank J.; Dickson, Andrew G.; Wanninkhof, Rik; Murata, Akihiko; Miller, Lisa A.; Greeley, Dana

2012-09-01

Based on measurements from the WOCE/JGOFS global CO2 survey, the CLIVAR/CO2 Repeat Hydrography Program and the Canadian Line P survey, we have observed an average decrease of 0.34% yr-1 in the saturation state of surface seawater in the Pacific Ocean with respect to aragonite and calcite. The upward migrations of the aragonite and calcite saturation horizons, averaging about 1 to 2 m yr-1, are the direct result of the uptake of anthropogenic CO2 by the oceans and regional changes in circulation and biogeochemical processes. The shoaling of the saturation horizon is regionally variable, with more rapid shoaling in the South Pacific where there is a larger uptake of anthropogenic CO2. In some locations, particularly in the North Pacific Subtropical Gyre and in the California Current, the decadal changes in circulation can be the dominant factor in controlling the migration of the saturation horizon. If CO2 emissions continue as projected over the rest of this century, the resulting changes in the marine carbonate system would mean that many coral reef systems in the Pacific would no longer be able to sustain a sufficiently high rate of calcification to maintain the viability of these ecosystems as a whole, and these changes perhaps could seriously impact the thousands of marine species that depend on them for survival.

Severity of ocean acidification following the end-Cretaceous asteroid impact

PubMed Central

Tyrrell, Toby; Armstrong McKay, David Ian

2015-01-01

Most paleo-episodes of ocean acidification (OA) were either too slow or too small to be instructive in predicting near-future impacts. The end-Cretaceous event (66 Mya) is intriguing in this regard, both because of its rapid onset and also because many pelagic calcifying species (including 100% of ammonites and more than 90% of calcareous nannoplankton and foraminifera) went extinct at this time. Here we evaluate whether extinction-level OA could feasibly have been produced by the asteroid impact. Carbon cycle box models were used to estimate OA consequences of (i) vaporization of up to 60 × 1015 mol of sulfur from gypsum rocks at the point of impact; (ii) generation of up to 5 × 1015 mol of NOx by the impact pressure wave and other sources; (iii) release of up to 6,500 Pg C as CO2 from vaporization of carbonate rocks, wildfires, and soil carbon decay; and (iv) ocean overturn bringing high-CO2 water to the surface. We find that the acidification produced by most processes is too weak to explain calcifier extinctions. Sulfuric acid additions could have made the surface ocean extremely undersaturated (Ωcalcite <0.5), but only if they reached the ocean very rapidly (over a few days) and if the quantity added was at the top end of literature estimates. We therefore conclude that severe ocean acidification might have been, but most likely was not, responsible for the great extinctions of planktonic calcifiers and ammonites at the end of the Cretaceous. PMID:25964350

Severity of ocean acidification following the end-Cretaceous asteroid impact.

PubMed

Tyrrell, Toby; Merico, Agostino; Armstrong McKay, David Ian

2015-05-26

Most paleo-episodes of ocean acidification (OA) were either too slow or too small to be instructive in predicting near-future impacts. The end-Cretaceous event (66 Mya) is intriguing in this regard, both because of its rapid onset and also because many pelagic calcifying species (including 100% of ammonites and more than 90% of calcareous nannoplankton and foraminifera) went extinct at this time. Here we evaluate whether extinction-level OA could feasibly have been produced by the asteroid impact. Carbon cycle box models were used to estimate OA consequences of (i) vaporization of up to 60 × 10(15) mol of sulfur from gypsum rocks at the point of impact; (ii) generation of up to 5 × 10(15) mol of NOx by the impact pressure wave and other sources; (iii) release of up to 6,500 Pg C as CO2 from vaporization of carbonate rocks, wildfires, and soil carbon decay; and (iv) ocean overturn bringing high-CO2 water to the surface. We find that the acidification produced by most processes is too weak to explain calcifier extinctions. Sulfuric acid additions could have made the surface ocean extremely undersaturated (Ωcalcite <0.5), but only if they reached the ocean very rapidly (over a few days) and if the quantity added was at the top end of literature estimates. We therefore conclude that severe ocean acidification might have been, but most likely was not, responsible for the great extinctions of planktonic calcifiers and ammonites at the end of the Cretaceous.

90Sr, 137Cs and (239,240)Pu concentration surface water time series in the Pacific and Indian Oceans--WOMARS results.

PubMed

Povinec, Pavel P; Aarkrog, Asker; Buesseler, Ken O; Delfanti, Roberta; Hirose, Katsumi; Hong, Gi Hoon; Ito, Toshimichi; Livingston, Hugh D; Nies, Hartmut; Noshkin, Victor E; Shima, Shigeki; Togawa, Orihiko

2005-01-01

Under an IAEA's Co-ordinated Research Project "Worldwide Marine Radioactivity Studies (WOMARS)" 90Sr, 137Cs and (239,240)Pu concentration surface water time series in the Pacific and Indian Oceans have been investigated. The Pacific and Indian Oceans were divided into 17 latitudinal boxes according to ocean circulation, global fallout patterns and the location of nuclear weapons test sites. The present levels and time trends in radionuclide concentrations in surface water for each box were studied and the corresponding effective half-lives were estimated. For the year 2000, the estimated average 90Sr, 137Cs and (239,240)Pu concentrations in surface waters of the Pacific and Indian Oceans varied from 0.1 to 1.5 mBq/L, 0.1 to 2.8 mBq/L, and 0.1 to 5.2 microBq/L, respectively. The mean effective half-lives for 90Sr and 137Cs in surface water were 12+/-1 years for the North, 20+/-1 years for the South and 21+/-2 years for the Equatorial Pacific. For (239,240)Pu the corresponding mean effective half-lives were 7+/-1 years for the North, 12+/-4 years for the South and 10+/-2 years for the Equatorial Pacific. For the Indian Ocean the mean effective half-lives of 137Cs and (239,240)Pu were 21+/-2 years and 9+/-1 years, respectively. There is evidence that fallout removal rates before 1970 were faster than those observed during recent decades. The estimated surface water concentrations of 90Sr, 137Cs and (239,240)Pu in latitudinal belts of the Pacific and Indian Oceans for the year 2000 may be used as the average levels so that any new contribution from nuclear facilities, nuclear weapons test sites, radioactive waste dumping sites and from possible nuclear accidents can be identified.

Seasonal carbonate chemistry covariation with temperature, oxygen, and salinity in a fjord estuary: implications for the design of ocean acidification experiments.

PubMed

Reum, Jonathan C P; Alin, Simone R; Feely, Richard A; Newton, Jan; Warner, Mark; McElhany, Paul

2014-01-01

Carbonate chemistry variability is often poorly characterized in coastal regions and patterns of covariation with other biologically important variables such as temperature, oxygen concentration, and salinity are rarely evaluated. This absence of information hampers the design and interpretation of ocean acidification experiments that aim to characterize biological responses to future pCO2 levels relative to contemporary conditions. Here, we analyzed a large carbonate chemistry data set from Puget Sound, a fjord estuary on the U.S. west coast, and included measurements from three seasons (winter, summer, and fall). pCO2 exceeded the 2008-2011 mean atmospheric level (392 µatm) at all depths and seasons sampled except for the near-surface waters (< 10 m) in the summer. Further, undersaturated conditions with respect to the biogenic carbonate mineral aragonite were widespread (Ωar<1). We show that pCO2 values were relatively uniform throughout the water column and across regions in winter, enriched in subsurface waters in summer, and in the fall some values exceeded 2500 µatm in near-surface waters. Carbonate chemistry covaried to differing levels with temperature and oxygen depending primarily on season and secondarily on region. Salinity, which varied little (27 to 31), was weakly correlated with carbonate chemistry. We illustrate potential high-frequency changes in carbonate chemistry, temperature, and oxygen conditions experienced simultaneously by organisms in Puget Sound that undergo diel vertical migrations under present-day conditions. We used simple calculations to estimate future pCO2 and Ωar values experienced by diel vertical migrators based on an increase in atmospheric CO2. Given the potential for non-linear interactions between pCO2 and other abiotic variables on physiological and ecological processes, our results provide a basis for identifying control conditions in ocean acidification experiments for this region, but also highlight the wide range of carbonate chemistry conditions organisms may currently experience in this and similar coastal ecosystems.

Seasonal Carbonate Chemistry Covariation with Temperature, Oxygen, and Salinity in a Fjord Estuary: Implications for the Design of Ocean Acidification Experiments

PubMed Central

Reum, Jonathan C. P.; Alin, Simone R.; Feely, Richard A.; Newton, Jan; Warner, Mark; McElhany, Paul

2014-01-01

Carbonate chemistry variability is often poorly characterized in coastal regions and patterns of covariation with other biologically important variables such as temperature, oxygen concentration, and salinity are rarely evaluated. This absence of information hampers the design and interpretation of ocean acidification experiments that aim to characterize biological responses to future pCO2 levels relative to contemporary conditions. Here, we analyzed a large carbonate chemistry data set from Puget Sound, a fjord estuary on the U.S. west coast, and included measurements from three seasons (winter, summer, and fall). pCO2 exceeded the 2008–2011 mean atmospheric level (392 µatm) at all depths and seasons sampled except for the near-surface waters (< 10 m) in the summer. Further, undersaturated conditions with respect to the biogenic carbonate mineral aragonite were widespread (Ωar<1). We show that pCO2 values were relatively uniform throughout the water column and across regions in winter, enriched in subsurface waters in summer, and in the fall some values exceeded 2500 µatm in near-surface waters. Carbonate chemistry covaried to differing levels with temperature and oxygen depending primarily on season and secondarily on region. Salinity, which varied little (27 to 31), was weakly correlated with carbonate chemistry. We illustrate potential high-frequency changes in carbonate chemistry, temperature, and oxygen conditions experienced simultaneously by organisms in Puget Sound that undergo diel vertical migrations under present-day conditions. We used simple calculations to estimate future pCO2 and Ωar values experienced by diel vertical migrators based on an increase in atmospheric CO2. Given the potential for non-linear interactions between pCO2 and other abiotic variables on physiological and ecological processes, our results provide a basis for identifying control conditions in ocean acidification experiments for this region, but also highlight the wide range of carbonate chemistry conditions organisms may currently experience in this and similar coastal ecosystems. PMID:24586915

The Carbon Cycle: Implications for Climate Change and Congress

DTIC Science & Technology

2008-03-13

burning of fossil fuels, deforestation , and other land use activities, have significantly altered the carbon cycle. As a result, atmospheric...80% of human-related CO2 emissions results from fossil fuel combustion, and 20% from land use change (primarily deforestation ). Fossil fuel burning...warming the planet. At present, the oceans and land surface are acting as sinks for CO2 emitted from fossil fuel combustion and deforestation , but

The Flux-Anomaly-Forced Model Intercomparison Project (FAFMIP) Contribution to CMIP6: Investigation of Sea-Level and Ocean Climate Change in Response to CO2 Forcing

NASA Technical Reports Server (NTRS)

Gregory, Jonathan M.; Bouttes, Nathaelle; Griffies, Stephen M.; Haak, Helmuth; Hurlin, William J.; Jungclaus, Johann; Kelley, Maxwell; Lee, Warren G.; Marshall, John; Romanou, Anastasia;

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

NASA Astrophysics Data System (ADS)

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.

Redox-controlled carbon and phosphorus burial: A mechanism for enhanced organic carbon sequestration during the PETM

NASA Astrophysics Data System (ADS)

Komar, Nemanja; Zeebe, Richard E.

2017-12-01

Geological records reveal a major perturbation in carbon cycling during the Paleocene-Eocene Thermal Maximum (PETM, ∼56 Ma), marked by global warming of more than 5 °C and a prominent negative carbon isotope excursion of at least 2.5‰ within the marine realm. The entire event lasted about 200,000 yr and was associated with a massive release of light carbon into the ocean-atmosphere system over several thousands of years. Here we focus on the terminal stage of the PETM, during which the ocean-atmosphere system rapidly recovered from the carbon cycle perturbation. We employ a carbon-cycle box model to examine the feedbacks between surface ocean biological production, carbon, oxygen, phosphorus, and carbonate chemistry during massive CO2 release events, such as the PETM. The model results indicate that the redox-controlled carbon-phosphorus feedback is capable of producing enhanced organic carbon sequestration during large carbon emission events. The locale of carbon oxidation (ocean vs. atmosphere) does not affect the amount of carbon sequestered. However, even though the model produces trends consistent with oxygen, excess accumulation rates of organic carbon (∼1700 Pg C during the recovery stage), export production and δ13 C data, it fails to reproduce the magnitude of change of sediment carbonate content and the CCD over-deepening during the recovery stage. The CCD and sediment carbonate content overshoot during the recovery stage is muted by a predicted increase in CaCO3 rain. Nonetheless, there are indications that the CaCO3 export remained relatively constant during the PETM. If this was indeed true, then an initial pulse of 3,000 Pg C followed by an additional, slow leak of 2,500 Pg C could have triggered an accelerated nutrient supply to the surface ocean instigating enhanced organic carbon export, consequently increasing organic carbon sequestration, resulting in an accelerated restoration of ocean-atmosphere biogeochemistry during the termination phase of the PETM.

Deep oceans may acidify faster than anticipated due to global warming

NASA Astrophysics Data System (ADS)

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.

The Carbon Isotopic Record of The C37:2 Alkenone In Sediments From The Equatorial and South Atlantic: Last Glacial Maximum (lgm) Vs. Holocene

NASA Astrophysics Data System (ADS)

Benthien, A.; Schulte, S.; Andersen, N.; Müller, P. J.; Schneider, R. R.

The carbon isotopic signal of the C37-alkenone, a taxon-specific biomarker for hap- tophyte algae, has been used in various paleoceanographic studies as a proxy for an- cient surface water CO2 concentration ([CO2aq]). However, a number of recent cul- ture, field and sediment studies imply that the carbon isotopic fractionation (ep) of alkenones is controlled predominantly by physiological processes and environmental factors other than the ambient CO2 concentration (i.e., growth rate, nutrient availabil- ity, light intensity, active carbon uptake, bicarbonate utilisation). The environmental conditions controlling phytoplankton growth are likely to vary strongly with oceano- graphic setting. Culture experiments can not perfectly recreate natural growth con- ditions and physical processes which affect the carbon isotopic signal in the field and its preservation in the sediment. Consequently, the use of the carbon isotopic record of alkenones as a reliable paleoceonographic proxy also requires sediment- based studies covering a broad range of different oceanic regimes for the past and modern ocean. Here, we present the first basin-wide comparison of alkenone ep val- ues from sediments of the Last Glacial Maximum (LGM) and the latest Holocene. Different oceanographic regions from the equatorial and South Atlantic Ocean were examined. Generally, alkenone ep is lower during the LGM compared to the Holocene. Considering present understanding of LGM-Holocene changes in surface water condi- tions, the observed glacial/interglacial difference in ep indicates that different effects controlled the isotopic fractionation in alkenone-producing algae depending on the regional setting. In upwelling regions, the variations in ep probably reflect a glacial increase in haptophyte productivity controlled by the availability of surface water nu- trient concentrations. By contrast, in oligotrophic areas slightly lower nutrient content was available during LGM. Here, the observed ep difference can be explained partly with an assumed glacial decrease in surface water [CO2aq]. However, it can not be ruled out that changes in haptophyte productivity also affected the ep signal to some extent. This study clearly demonstrates that a reliable reconstruction of [CO2aq] on the basis of the isotopic composition of alkenones is not feasible without a detailed 1 knowledge of ancient haptophyte growth conditions. 2

Terrestrial cooling in Northern Europe during the eocene-oligocene transition.

PubMed

Hren, Michael T; Sheldon, Nathan D; Grimes, Stephen T; Collinson, Margaret E; Hooker, Jerry J; Bugler, Melanie; Lohmann, Kyger C

2013-05-07

Geochemical and modeling studies suggest that the transition from the "greenhouse" state of the Late Eocene to the "icehouse" conditions of the Oligocene 34-33.5 Ma was triggered by a reduction of atmospheric pCO2 that enabled the rapid buildup of a permanent ice sheet on the Antarctic continent. Marine records show that the drop in pCO2 during this interval was accompanied by a significant decline in high-latitude sea surface and deep ocean temperature and enhanced seasonality in middle and high latitudes. However, terrestrial records of this climate transition show heterogeneous responses to changing pCO2 and ocean temperatures, with some records showing a significant time lag in the temperature response to declining pCO2. We measured the Δ47 of aragonite shells of the freshwater gastropod Viviparus lentus from the Solent Group, Hampshire Basin, United Kingdom, to reconstruct terrestrial temperature and hydrologic change in the North Atlantic region during the Eocene-Oligocene transition. Our data show a decrease in growing-season surface water temperatures (~10 °C) during the Eocene-Oligocene transition, corresponding to an average decrease in mean annual air temperature of ~4-6 °C from the Late Eocene to Early Oligocene. The magnitude of cooling is similar to observed decreases in North Atlantic sea surface temperature over this interval and occurs during major glacial expansion. This suggests a close linkage between atmospheric carbon dioxide concentrations, Northern Hemisphere temperature, and expansion of the Antarctic ice sheets.

Reducing energy-related CO2 emissions using accelerated weathering of limestone

USGS Publications Warehouse

Rau, Greg H.; Knauss, Kevin G.; Langer, William H.; Caldeira, Ken

2007-01-01

The use and impacts of accelerated weathering of limestone (AWL; reaction: CO2+H2O+CaCO3→Ca2++2(HCO3-) is explored as a CO2 capture and sequestration method. It is shown that significant limestone resources are relatively close to a majority of CO2-emitting power plants along the coastal US, a favored siting location for AWL. Waste fines, representing more than 20% of current US crushed limestone production (>109 tonnes/yr), could provide an inexpensive or free source of AWL carbonate. With limestone transportation then as the dominant cost variable, CO2 mitigation costs of $3-$4/tonne appear to be possible in certain locations. Perhaps 10–20% of US point–source CO2 emissions could be mitigated in this fashion. It is experimentally shown that CO2 sequestration rates of 10-6 to 10-5 moles/sec per m2 of limestone surface area are achievable, with reaction densities on the order of 10-2 tonnes CO2 m-3day-1, highly dependent on limestone particle size, solution turbulence and flow, and CO2 concentration. Modeling shows that AWL would allow carbon storage in the ocean with significantly reduced impacts to seawater pH relative to direct CO2 disposal into the atmosphere or sea. The addition of AWL-derived alkalinity to the ocean may itself be beneficial for marine biota.

Transient Earth system responses to cumulative carbon dioxide emissions: linearities, uncertainties, and probabilities in an observation-constrained model ensemble

NASA Astrophysics Data System (ADS)

Steinacher, M.; Joos, F.

2016-02-01

Information on the relationship between cumulative fossil CO2 emissions and multiple climate targets is essential to design emission mitigation and climate adaptation strategies. In this study, the transient response of a climate or environmental variable per trillion tonnes of CO2 emissions, termed TRE, is quantified for a set of impact-relevant climate variables and from a large set of multi-forcing scenarios extended to year 2300 towards stabilization. An ˜ 1000-member ensemble of the Bern3D-LPJ carbon-climate model is applied and model outcomes are constrained by 26 physical and biogeochemical observational data sets in a Bayesian, Monte Carlo-type framework. Uncertainties in TRE estimates include both scenario uncertainty and model response uncertainty. Cumulative fossil emissions of 1000 Gt C result in a global mean surface air temperature change of 1.9 °C (68 % confidence interval (c.i.): 1.3 to 2.7 °C), a decrease in surface ocean pH of 0.19 (0.18 to 0.22), and a steric sea level rise of 20 cm (13 to 27 cm until 2300). Linearity between cumulative emissions and transient response is high for pH and reasonably high for surface air and sea surface temperatures, but less pronounced for changes in Atlantic meridional overturning, Southern Ocean and tropical surface water saturation with respect to biogenic structures of calcium carbonate, and carbon stocks in soils. The constrained model ensemble is also applied to determine the response to a pulse-like emission and in idealized CO2-only simulations. The transient climate response is constrained, primarily by long-term ocean heat observations, to 1.7 °C (68 % c.i.: 1.3 to 2.2 °C) and the equilibrium climate sensitivity to 2.9 °C (2.0 to 4.2 °C). This is consistent with results by CMIP5 models but inconsistent with recent studies that relied on short-term air temperature data affected by natural climate variability.

Ocean Acidification from space: recent advances

NASA Astrophysics Data System (ADS)

Sabia, Roberto; Shutler, Jamie; Land, Peter; Fernandez-Prieto, Diego; Donlon, Craig; Reul, Nicolas

2017-04-01

The phenomenon referred to as Ocean Acidification (OA) is gathering increasing attention as one of the major foci of climate-related research, for its profound impact at scientific and socio-economic level. To date, the majority of the scientific studies into the potential impacts of OA have focused on in-situ measurements, laboratory-controlled experiments and models simulations. Satellite remote sensing technology have yet to be fully exploited, despite it has been stressed it could play a significant role by providing synoptic and frequent measurements for investigating globally OA processes, also extending in-situ carbonate chemistry measurements on different spatial/temporal scales [1,2]. Within this context, the purpose of the recently completed ESA "Pathfinders - Ocean Acidification" project was to quantitatively and routinely estimate OA-related parameters by means of a blending of satellite observations and model outputs in five case-study regions (global ocean, Amazon plume, Barents sea, Greater Caribbean and Bay of Bengal). Satellite Ocean Colour, Sea Surface Temperature (SST) and Sea Surface Salinity (SSS) have been exploited, with an emphasis on the latter being the latest addition to the portfolio of satellite measured parameters. A proper merging of these different satellites products allows computing at least two independent proxies among the seawater carbonate system parameters: the partial pressure of CO2 in surface seawater (pCO2); the total Dissolved Inorganic Carbon (DIC), the total alkalinity (TA) and the surface ocean pH. In the project, efforts have been devoted to a systematic characterization of TA and DIC from space in the mentioned case-study regions; in this paper, also through the knowledge of these parameters, the objective is to come up with the currently best educated guess of the surface ocean pH [3] and Aragonite saturation state. This will also include an estimation of the achievable accuracy by propagating the errors in the satellite data sources. The overarching long-term objectives are to develop new algorithms and data processing strategies to overcome the relative immaturity of OA satellite products currently available, and to produce a global, temporally evolving, quasi-operational suite of OA satellite-derived data. References: [1] Land, P., J. Shutler, H. Findlay, F. Girard-Ardhuin, R. Sabia, N. Reul, J.-F. Piolle, B. Chapron, Y. Quilfen, J. Salisbury, D. Vandemark, R. Bellerby, and P. Bhadury, "Salinity from space unlocks satellite-based assessment of ocean acidification", Environmental Science & Technology, DOI: 10.1021/es504849s, Publication Date (Web): January 8, 2015 [2] Salisbury, J., D. Vandemark, B. Jönsson, W. Balch, S. Chakraborty, S. Lohrenz, B. Chapron, B. Hales, A. Mannino, J.T. Mathis, N. Reul, S.R. Signorini, R. Wanninkhof, and K.K. Yates. 2015. How can present and future satellite missions support scientific studies that address ocean acidification? Oceanography 28(2):108-121, http://dx.doi.org/10.5670/oceanog.2015.35. [3] Sabia R., D. Fernández-Prieto, J. Shutler, C. Donlon, P. Land, N. Reul, Remote Sensing of Surface Ocean pH Exploiting Sea Surface Salinity Satellite Observations, IGARSS '15 (International Geoscience and Remote Sensing Symposium), Milano, Italy, July 27 -31, 2015.

Palaeoceanography. Antarctic stratification and glacial CO2.

PubMed

Keeling, R F; Visbeck, M

2001-08-09

One way of accounting for lowered atmospheric carbon dioxide concentrations during Pleistocene glacial periods is by invoking the Antarctic stratification hypothesis, which links the reduction in CO2 to greater stratification of ocean surface waters around Antarctica. As discussed by Sigman and Boyle, this hypothesis assumes that increased stratification in the Antarctic zone (Fig. 1) was associated with reduced upwelling of deep waters around Antarctica, thereby allowing CO2 outgassing to be suppressed by biological production while also allowing biological production to decline, which is consistent with Antarctic sediment records. We point out here, however, that the response of ocean eddies to increased Antarctic stratification can be expected to increase, rather than reduce, the upwelling rate of deep waters around Antarctica. The stratification hypothesis may have difficulty in accommodating eddy feedbacks on upwelling within the constraints imposed by reconstructions of winds and Antarctic-zone productivity in glacial periods.

Distribution of Nitrogen Compounds in Marine Aerosol and Their Deposition Over the Pacific Ocean

NASA Astrophysics Data System (ADS)

Uematsu, M.; Narita, Y.; Sun, S. Y.

2016-02-01

Nutrient supply to the ocean surface layer is an important factor controlling the marine ecosystem. The major paths of supplies of nutrients have been considered as those from nutrient-rich deep waters and riverine input, which is mostly taken up near the estuary region, but the nutrients transported through the atmosphere recognize to be important for the open ocean, where the nutrients are limiting primary productivity. Because of rapid economic development surrounding the Pacific Ocean, anthropogenic NOx emissions increased by 2-3 times during the past decades. This rapid increase of NOx emission causes a large amount of N deposition mostly in the form of nitrate and ammonium over ocean surfaces, and strongly impacts their marine ecosystems. Especially, biological N2 fixation, riverine input and atmospheric deposition contribute to support "new production" and affect CO2 air-sea exchange. The concentration of nitrogen compounds in marine aerosol has been measured on the island stations and onboard of research vessels in the Pacific Ocean over a few decades. The temporal and spatial atmospheric distribution of water-soluble particulate nitrogen compounds is summarized in this study. As the transport of anthropogenic nitrogen compounds from land, high concentration is revealed over the marginal seas in the western North Pacific. Most of nitrate exists in the coarse aerosol associated with sea-salt particle while ammonium exists in the fine particle and showing a good relationship with non-sea-salt sulfate. This different particle size affects to estimate the deposition flux of nitrogen compounds to the ocean surface. Over the high primary productive areas such as the equatorial Pacific and the Southern Ocean, ammonia is released into the atmosphere and transported to other area. By wet and dry deposition, ammonium is removed to the ocean surface and modified the distribution of nitrogen compounds in the surface waters.

Ocean Acidification Refugia of the Florida Reef Tract

NASA Astrophysics Data System (ADS)

Manzello, D.; Enochs, I.; Melo, N.; Gledhill, D. K.; Johns, E. M.

2012-12-01

Ocean acidification (OA) is expected to reduce the calcification rates of marine organisms, yet we have little understanding of how OA will manifest within dynamic, real-world systems. Natural CO2, alkalinity, and salinity gradients can significantly alter local carbonate chemistry, and thereby create a range of susceptibility for different ecosystems to OA. As such, there is a need to characterize this natural variability of seawater carbonate chemistry, especially within coastal ecosystems. Since 2009, carbonate chemistry data have been collected on the Florida Reef Tract (FRT). During periods of heightened productivity, there is a net uptake of total CO2 (TCO2) which increases aragonite saturation state (Ωarag) values on inshore patch reefs of the upper FRT. These waters can exhibit greater Ωarag than what has been modeled for the tropical surface ocean during preindustrial times, with mean (± std. error) Ωarag-values in spring = 4.69 (± 0.101). Conversely, Ωarag-values on offshore reefs generally represent oceanic carbonate chemistries consistent with present day tropical surface ocean conditions. This gradient is opposite from what has been reported for other reef environments. We hypothesize this pattern is caused by the photosynthetic uptake of TCO2 mainly by seagrasses and, to a lesser extent, macroalgae in the inshore waters of the FRT. These inshore reef habitats are therefore potential acidification refugia that are defined not only in a spatial sense, but also in time; coinciding with seasonal productivity dynamics. Coral reefs located within or immediately downstream of seagrass beds may find refuge from OA.

Ocean Acidification Refugia of the Florida Reef Tract

PubMed Central

Manzello, Derek P.; Enochs, Ian C.; Melo, Nelson; Gledhill, Dwight K.; Johns, Elizabeth M.

2012-01-01

Ocean acidification (OA) is expected to reduce the calcification rates of marine organisms, yet we have little understanding of how OA will manifest within dynamic, real-world systems. Natural CO2, alkalinity, and salinity gradients can significantly alter local carbonate chemistry, and thereby create a range of susceptibility for different ecosystems to OA. As such, there is a need to characterize this natural variability of seawater carbonate chemistry, especially within coastal ecosystems. Since 2009, carbonate chemistry data have been collected on the Florida Reef Tract (FRT). During periods of heightened productivity, there is a net uptake of total CO2 (TCO2) which increases aragonite saturation state (Ωarag) values on inshore patch reefs of the upper FRT. These waters can exhibit greater Ωarag than what has been modeled for the tropical surface ocean during preindustrial times, with mean (± std. error) Ωarag-values in spring = 4.69 (±0.101). Conversely, Ωarag-values on offshore reefs generally represent oceanic carbonate chemistries consistent with present day tropical surface ocean conditions. This gradient is opposite from what has been reported for other reef environments. We hypothesize this pattern is caused by the photosynthetic uptake of TCO2 mainly by seagrasses and, to a lesser extent, macroalgae in the inshore waters of the FRT. These inshore reef habitats are therefore potential acidification refugia that are defined not only in a spatial sense, but also in time; coinciding with seasonal productivity dynamics. Coral reefs located within or immediately downstream of seagrass beds may find refuge from OA. PMID:22848575

Ocean acidification refugia of the Florida Reef Tract.

PubMed

Manzello, Derek P; Enochs, Ian C; Melo, Nelson; Gledhill, Dwight K; Johns, Elizabeth M

2012-01-01

Ocean acidification (OA) is expected to reduce the calcification rates of marine organisms, yet we have little understanding of how OA will manifest within dynamic, real-world systems. Natural CO(2), alkalinity, and salinity gradients can significantly alter local carbonate chemistry, and thereby create a range of susceptibility for different ecosystems to OA. As such, there is a need to characterize this natural variability of seawater carbonate chemistry, especially within coastal ecosystems. Since 2009, carbonate chemistry data have been collected on the Florida Reef Tract (FRT). During periods of heightened productivity, there is a net uptake of total CO(2) (TCO(2)) which increases aragonite saturation state (Ω(arag)) values on inshore patch reefs of the upper FRT. These waters can exhibit greater Ω(arag) than what has been modeled for the tropical surface ocean during preindustrial times, with mean (± std. error) Ω(arag)-values in spring = 4.69 (±0.101). Conversely, Ω(arag)-values on offshore reefs generally represent oceanic carbonate chemistries consistent with present day tropical surface ocean conditions. This gradient is opposite from what has been reported for other reef environments. We hypothesize this pattern is caused by the photosynthetic uptake of TCO(2) mainly by seagrasses and, to a lesser extent, macroalgae in the inshore waters of the FRT. These inshore reef habitats are therefore potential acidification refugia that are defined not only in a spatial sense, but also in time; coinciding with seasonal productivity dynamics. Coral reefs located within or immediately downstream of seagrass beds may find refuge from OA.

Climate-driven changes to the atmospheric CO2 sink in the subtropical North Pacific Ocean.

PubMed

Dore, John E; Lukas, Roger; Sadler, Daniel W; Karl, David M

2003-08-14

The oceans represent a significant sink for atmospheric carbon dioxide. Variability in the strength of this sink occurs on interannual timescales, as a result of regional and basin-scale changes in the physical and biological parameters that control the flux of this greenhouse gas into and out of the surface mixed layer. Here we analyse a 13-year time series of oceanic carbon dioxide measurements from station ALOHA in the subtropical North Pacific Ocean near Hawaii, and find a significant decrease in the strength of the carbon dioxide sink over the period 1989-2001. We show that much of this reduction in sink strength can be attributed to an increase in the partial pressure of surface ocean carbon dioxide caused by excess evaporation and the accompanying concentration of solutes in the water mass. Our results suggest that carbon dioxide uptake by ocean waters can be strongly influenced by changes in regional precipitation and evaporation patterns brought on by climate variability.

Autumn photoproduction of carbon monoxide in Jiaozhou Bay, China

NASA Astrophysics Data System (ADS)

Ren, Chunyan; Yang, Guipeng; Lu, Xiaolan

2014-06-01

Carbon monoxide (CO) plays a significant role in global warming and atmospheric chemistry. Global oceans are net natural sources of atmospheric CO. CO at surface ocean is primarily produced from the photochemical degradation of chromophoric dissolved organic matter (CDOM). In this study, the effects of photobleaching, temperature and the origin (terrestrial or marine) of CDOM on the apparent quantum yields (AQY) of CO were studied for seawater samples collected from Jiaozhou Bay. Our results demonstrat that photobleaching, temperature and the origin of CDOM strongly affected the efficiency of CO photoproduction. The concentration, absorbance and fluorescence of CDOM exponentially decreased with increasing light dose. Terrestrial riverine organic matter could be more prone to photodegradation than the marine algae-derived one. The relationships between CO AQY and the dissolved organic carbon-specific absorption coefficient at 254 nm for the photobleaching study were nonlinear, whereas those of the original samples were strongly linear. This suggests that: 1) terrestrial riverine CDOM was more efficient than marine algae-derived CDOM for CO photoproduction; 2) aromatic and olefinic moieties of the CDOM pool were affected more strongly by degradation processes than by aliphatic ones. Water temperature and the origin of CDOM strongly affected the efficiency of CO photoproduction. The photoproduction rate of CO in autumn was estimated to be 31.98 μmol m-2 d-1 and the total DOC photomineralization was equivalent to 3.25%-6.35% of primary production in Jiaozhou Bay. Our results indicate that CO photochemistry in coastal areas is important for oceanic carbon cycle.

Volcanic ash as a driver of enhanced organic carbon burial in the Cretaceous.

PubMed

Lee, Cin-Ty A; Jiang, Hehe; Ronay, Elli; Minisini, Daniel; Stiles, Jackson; Neal, Matthew

2018-03-08

On greater than million year timescales, carbon in the ocean-atmosphere-biosphere system is controlled by geologic inputs of CO 2 through volcanic and metamorphic degassing. High atmospheric CO 2 and warm climates in the Cretaceous have been attributed to enhanced volcanic emissions of CO 2 through more rapid spreading at mid-ocean ridges and, in particular, to a global flare-up in continental arc volcanism. Here, we show that global flare-ups in continental arc magmatism also enhance the global flux of nutrients into the ocean through production of windblown ash. We show that up to 75% of Si, Fe and P is leached from windblown ash during and shortly after deposition, with soluble Si, Fe and P inputs from ash alone in the Cretaceous being higher than the combined input of dust and rivers today. Ash-derived nutrient inputs may have increased the efficiency of biological productivity and organic carbon preservation in the Cretaceous, possibly explaining why the carbon isotopic signature of Cretaceous seawater was high. Variations in volcanic activity, particularly continental arcs, have the potential of profoundly altering carbon cycling at the Earth's surface by increasing inputs of CO 2 and ash-borne nutrients, which together enhance biological productivity and burial of organic carbon, generating an abundance of hydrocarbon source rocks.

Imposing strong constraints on tropical terrestrial CO2 fluxes using passenger aircraft based measurements

NASA Astrophysics Data System (ADS)

Niwa, Yosuke; Machida, Toshinobu; Sawa, Yousuke; Matsueda, Hidekazu; Schuck, Tanja J.; Brenninkmeijer, Carl A. M.; Imasu, Ryoichi; Satoh, Masaki

2012-06-01

Because very few measurements of atmospheric carbon dioxide (CO2) are available in the tropics, estimates of surface CO2 fluxes in tropical regions are beset with considerable uncertainties. To improve estimates of tropical terrestrial fluxes, atmospheric CO2 inversion was performed using passenger aircraft based measurements of the Comprehensive Observation Network for Trace gases by Airliner (CONTRAIL) project in addition to the surface measurement data set of GLOBALVIEW-CO2. Regional monthly fluxes at the earth's surface were estimated using the Bayesian synthesis approach focusing on the period 2006-2008 using the Nonhydrostatic Icosahedral Atmospheric Model-based Transport Model (NICAM-TM). By adding the aircraft to the surface data, the posterior flux errors were greatly reduced; specifically, error reductions of up to 64% were found for tropical Asia regions. This strong impact is closely related to efficient vertical transport in the tropics. The optimized surface fluxes using the CONTRAIL data were evaluated by comparing the simulated atmospheric CO2 distributions with independent aircraft measurements of the Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container (CARIBIC) project. The inversion with the CONTRAIL data yields the global carbon sequestration rates of 2.22 ± 0.28 Pg C yr-1 for the terrestrial biosphere and 2.24 ± 0.27 Pg C yr-1 for the oceans (the both are adjusted by riverine input of CO2). For the first time the CONTRAIL CO2 measurements were used in an inversion system to identify the areas of greatest impact in terms of reducing flux uncertainties.

Efficiency of small scale carbon mitigation by patch iron fertilization

NASA Astrophysics Data System (ADS)

Sarmiento, J. L.; Slater, R. D.; Dunne, J.; Gnanadesikan, A.; Hiscock, M. R.

2009-11-01

While nutrient depletion scenarios have long shown that the high-latitude High Nutrient Low Chlorophyll (HNLC) regions are the most effective for sequestering atmospheric carbon dioxide, recent simulations with prognostic biogeochemical models have suggested that only a fraction of the potential drawdown can be realized. We use a global ocean biogeochemical general circulation model developed at GFDL and Princeton to examine this and related issues. We fertilize two patches in the North and Equatorial Pacific, and two additional patches in the Southern Ocean HNLC region north of the biogeochemical divide and in the Ross Sea south of the biogeochemical divide. We obtain by far the greatest response to iron fertilization at the Ross Sea site. Here the CO2 remains sequestered on century time-scales and the efficiency of fertilization remains almost constant no matter how frequently iron is applied as long as it is confined to the growing season. The second most efficient site is in the Southern Ocean. Here the biological response to iron fertilization is comparable to the Ross Sea, but the enhanced biological uptake of CO2 is more spread out in the vertical and thus less effective at leading to removal of CO2 from the atmosphere. The North Pacific site has lower initial nutrients and thus a lower efficiency. Fertilization of the Equatorial Pacific leads to an expansion of the suboxic zone and a striking increase in denitrification that causes a sharp reduction in overall surface biological export production and CO2 uptake. The impacts on the oxygen distribution and surface biological export are less prominent at other sites, but nevertheless still a source of concern. The century time scale retention of iron in these models greatly increases the long-term biological response to iron addition as compared with models in which the added iron is rapidly scavenged from the ocean.

Ocean acidification causes structural deformities in juvenile coral skeletons.

PubMed

Foster, Taryn; Falter, James L; McCulloch, Malcolm T; Clode, Peta L

2016-02-01

Rising atmospheric CO2 is causing the oceans to both warm and acidify, which could reduce the calcification rates of corals globally. Successful coral recruitment and high rates of juvenile calcification are critical to the replenishment and ultimate viability of coral reef ecosystems. Although elevated Pco2 (partial pressure of CO2) has been shown to reduce the skeletal weight of coral recruits, the structural changes caused by acidification during initial skeletal deposition are unknown. We show, using high-resolution three-dimensional x-ray microscopy, that ocean acidification (Pco2 ~900 μatm, pH ~7.7) not only causes reduced overall mineral deposition but also a deformed and porous skeletal structure in newly settled coral recruits. In contrast, elevated temperature (+3°C) had little effect on skeletal formation except to partially mitigate the effects of elevated Pco2. The striking structural deformities we observed show that new recruits are at significant risk, being unable to effectively build their skeletons in the Pco2 conditions predicted to occur for open ocean surface waters under a "business-as-usual" emissions scenario [RCP (representative concentration pathway) 8.5] by the year 2100.

Ocean acidification causes structural deformities in juvenile coral skeletons

PubMed Central

Foster, Taryn; Falter, James L.; McCulloch, Malcolm T.; Clode, Peta L.

2016-01-01

Rising atmospheric CO2 is causing the oceans to both warm and acidify, which could reduce the calcification rates of corals globally. Successful coral recruitment and high rates of juvenile calcification are critical to the replenishment and ultimate viability of coral reef ecosystems. Although elevated Pco2 (partial pressure of CO2) has been shown to reduce the skeletal weight of coral recruits, the structural changes caused by acidification during initial skeletal deposition are unknown. We show, using high-resolution three-dimensional x-ray microscopy, that ocean acidification (Pco2 ~900 μatm, pH ~7.7) not only causes reduced overall mineral deposition but also a deformed and porous skeletal structure in newly settled coral recruits. In contrast, elevated temperature (+3°C) had little effect on skeletal formation except to partially mitigate the effects of elevated Pco2. The striking structural deformities we observed show that new recruits are at significant risk, being unable to effectively build their skeletons in the Pco2 conditions predicted to occur for open ocean surface waters under a “business-as-usual” emissions scenario [RCP (representative concentration pathway) 8.5] by the year 2100. PMID:26989776

Geographical CO2 sensitivity of phytoplankton correlates with ocean buffer capacity.

PubMed

Richier, Sophie; Achterberg, Eric P; Humphreys, Matthew P; Poulton, Alex J; Suggett, David J; Tyrrell, Toby; Moore, C Mark

2018-05-25

Accumulation of anthropogenic CO 2 is significantly altering ocean chemistry. A range of biological impacts resulting from this oceanic CO 2 accumulation are emerging, however the mechanisms responsible for observed differential susceptibility between organisms and across environmental settings remain obscure. A primary consequence of increased oceanic CO 2 uptake is a decrease in the carbonate system buffer capacity, which characterises the system's chemical resilience to changes in CO 2 , generating the potential for enhanced variability in pCO 2 and the concentration of carbonate [CO 3 2- ], bicarbonate [HCO 3 - ] and protons [H + ] in the future ocean. We conducted a meta-analysis of 17 shipboard manipulation experiments performed across three distinct geographical regions that encompassed a wide range of environmental conditions from European temperate seas to Arctic and Southern oceans. These data demonstrated a correlation between the magnitude of natural phytoplankton community biological responses to short-term CO 2 changes and variability in the local buffer capacity across ocean basin scales. Specifically, short-term suppression of small phytoplankton (<10 μm) net growth rates were consistently observed under enhanced pCO 2 within experiments performed in regions with higher ambient buffer capacity. The results further highlight the relevance of phytoplankton cell size for the impacts of enhanced pCO 2 in both the modern and future ocean. Specifically, cell-size related acclimation and adaptation to regional environmental variability, as characterised by buffer capacity, likely influences interactions between primary producers and carbonate chemistry over a range of spatio-temporal scales. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.

Oceanic crustal carbon cycle drives 26-million-year atmospheric carbon dioxide periodicities.

PubMed

Müller, R Dietmar; Dutkiewicz, Adriana

2018-02-01

Atmospheric carbon dioxide (CO 2 ) data for the last 420 million years (My) show long-term fluctuations related to supercontinent cycles as well as shorter cycles at 26 to 32 My whose origin is unknown. Periodicities of 26 to 30 My occur in diverse geological phenomena including mass extinctions, flood basalt volcanism, ocean anoxic events, deposition of massive evaporites, sequence boundaries, and orogenic events and have previously been linked to an extraterrestrial mechanism. The vast oceanic crustal carbon reservoir is an alternative potential driving force of climate fluctuations at these time scales, with hydrothermal crustal carbon uptake occurring mostly in young crust with a strong dependence on ocean bottom water temperature. We combine a global plate model and oceanic paleo-age grids with estimates of paleo-ocean bottom water temperatures to track the evolution of the oceanic crustal carbon reservoir over the past 230 My. We show that seafloor spreading rates as well as the storage, subduction, and emission of oceanic crustal and mantle CO 2 fluctuate with a period of 26 My. A connection with seafloor spreading rates and equivalent cycles in subduction zone rollback suggests that these periodicities are driven by the dynamics of subduction zone migration. The oceanic crust-mantle carbon cycle is thus a previously overlooked mechanism that connects plate tectonic pulsing with fluctuations in atmospheric carbon and surface environments.

Oceanic crustal carbon cycle drives 26-million-year atmospheric carbon dioxide periodicities

PubMed Central

Müller, R. Dietmar; Dutkiewicz, Adriana

2018-01-01

Atmospheric carbon dioxide (CO2) data for the last 420 million years (My) show long-term fluctuations related to supercontinent cycles as well as shorter cycles at 26 to 32 My whose origin is unknown. Periodicities of 26 to 30 My occur in diverse geological phenomena including mass extinctions, flood basalt volcanism, ocean anoxic events, deposition of massive evaporites, sequence boundaries, and orogenic events and have previously been linked to an extraterrestrial mechanism. The vast oceanic crustal carbon reservoir is an alternative potential driving force of climate fluctuations at these time scales, with hydrothermal crustal carbon uptake occurring mostly in young crust with a strong dependence on ocean bottom water temperature. We combine a global plate model and oceanic paleo-age grids with estimates of paleo-ocean bottom water temperatures to track the evolution of the oceanic crustal carbon reservoir over the past 230 My. We show that seafloor spreading rates as well as the storage, subduction, and emission of oceanic crustal and mantle CO2 fluctuate with a period of 26 My. A connection with seafloor spreading rates and equivalent cycles in subduction zone rollback suggests that these periodicities are driven by the dynamics of subduction zone migration. The oceanic crust-mantle carbon cycle is thus a previously overlooked mechanism that connects plate tectonic pulsing with fluctuations in atmospheric carbon and surface environments. PMID:29457135

Environmental biogeography of near-surface phytoplankton in the southeast Pacific Ocean

NASA Astrophysics Data System (ADS)

Hardy, John; Hanneman, Andrew; Behrenfeldt, Michael; Horner, Rita

1996-10-01

Biogeographic interpretation of large-scale phytoplankton distribution patterns in relation to surface hydrography is essential to understanding pelagic food web dynamics and biogeochemical processes influencing global climate. We examined the abundance and biomass of phytoplankton in relation to physical and chemical parameters in the southeast Pacific Ocean. Samples were collected along longitude 110°W, between 10°N and 60°S during late austral summer. Patterns of taxa abundance and hydrographic variables were interpreted by principal components analysis. Five distinct phytohydrographic regions were identified: (i) a north equatorial region of moderate productivity dominated by small flagellates, low nitrate and low-to-moderate pCO 2; (ii) a south equatorial region characterized by high primary productivity dominated by diatoms, high nutrient levels, and relatively high pCO 2; (iii) a central gyre region characterized by low productivity dominated by small flagellates, low nitrate, and high pCO 2; (iv) a sub-Antarctic region with moderate productivity dominated by coccolithophores, moderate nitrate concentrations, and low pCO 2; and (v) an Antarctic region with high productivity dominated by diatoms, very high nitrate, and low pCO 2. Productivity and average phytoplankton cell size were positively correlated with nitrate concentration. Total phytoplankton abundance was negatively correlated with pCO 2, photosynthetically active radiation, and ultraviolet-B radiation. The interaction between phytoplankton carbon assimilation, atmospheric CO2, and the inhibitory effect of ultraviolet radiation could have implications for the global climate. These data suggest that the effects would be greatest at southern mid-latitudes (40-50°S) where present phytoplankton production and predicted future increases in UV-B are both relatively high.

The secret lives of corals: Climate records from coral chemistry

DOE Office of Scientific and Technical Information (OSTI.GOV)

Beck, J.W.; Smoker, M.; Burr, G.

1995-12-01

Corals can provide archives of a diverse suite of information about the ocean surface mixed layer, including records of ocean surface temperature (via coral Sr/Ca or U/Ca measurements), salinity (via {gamma}{sup 18}O measurements), biologic activity (via {gamma}{sup 13}C measurements), and ocean/atmosphere CO{sub 2} exchange rates (via {sup 14}C/{sup 12}C measurements). Recently, it has been shown that corals record evidence of large seasonal oscillations in {sup 14}C concentration of the ocean surface mixed layer, and that such oscillations are modulated by ENSO. These oscillations are related to seasonal changes in the surface wind velocity field, changes in the patterns of regionalmore » upwelling, as well as seasonal changes in the strength of the thermocline. High frequency AMS {sup 14}C analyses of corals shows that ENSO events can dramatically diminish the annual range in ocean mixed layer {sup 14}C concentration in this region. Our work on a coral from Vanuatu in the western equatorial Pacific also documents large seasonal changes in {sup 14}C concentration (3-5%) as well as ENSO modulation of these variations during the 82-83 ENSO event.« less

Revised budget for the oceanic uptake of anthropogenic carbon dioxide

USGS Publications Warehouse

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

1992-01-01

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

Melt focusing and CO2 extraction at mid-ocean ridges: simulations of reactive two-phase flow

NASA Astrophysics Data System (ADS)

Keller, T.; Katz, R. F.; Hirschmann, M. M.

2016-12-01

The deep CO2 cycle is the result of fluxes between near-surface and mantle reservoirs. Outgassing from mid-ocean ridges is one of the primary fluxes of CO2 from the asthenosphere into the ocean-atmosphere reservoir. Focusing of partial melt to the ridge axis crucially controls this flux. However, the role of volatiles, in particular CO2 and H2O, on melt transport processes beneath ridges remains poorly understood. We investigate this transport using numerical simulations of two-phase, multi-component magma/mantle dynamics. The phases are solid mantle and liquid magma; the components are dunite, MORB, hydrated basalt, and carbonated basalt. These effective components capture accepted features of mantle melting with volatiles. The fluid-dynamical model is McKenzie's formulation [1], while melting and reactive transport use the R_DMC method [2,3]. Our results indicate that volatiles cause channelized melt transport, which leads to significant variability in volume and composition of focused melt. The volatile-induced expansion of the melting regime at depth, however, has no influence on melt focusing; distal volatile-rich melts are not focused to the axis. Up to 50% of these melts are instead emplaced along the oceanic LAB. There, crystallization of accumulated melt leads to enrichment of CO2 and H2O in the deep lithosphere, which has implications for LAB rheology and volatile recycling by subduction. Results from a suite of simulations, constrained by catalogued observational data [4,5,6] enable predictions of global MOR CO2 output. By combining observational constraints with self-consistent numerical simulations we obtain a range of CO2 output from the global ridge system of 28-110 Mt CO2/yr, corresponding to mean CO2 contents of 50-200 ppm in the mantle. REFERENCES[1] McKenzie (1984), doi:10.1093/petrology/25.3.713.[2] Rudge, Bercovici & Spiegelman (2011), doi:10.1111/j.1365-246X.2010.04870.x.[3] Keller & Katz (2016), doi:10.1093/petrology/egw030.[4] Dalton, Langmuir & Gale (2014), doi:10.1126/science.1249466.[5] Gale, Langmuir & Dalton (2014), doi:10.1093/petrology/egu017.[6] White et al. (2001), doi:10.1093/petrology/42.6.1171. Fig: Simulation results of MOR magma/mantle dynamics with H2O and CO2, showing Darcy flux magnitude for half-spreading rates of 1 and 5 cm/yr.

Terrestrial aftermath of the Moon-forming impact.

PubMed

Sleep, Norman H; Zahnle, Kevin J; Lupu, Roxana E

2014-09-13

Much of the Earth's mantle was melted in the Moon-forming impact. Gases that were not partially soluble in the melt, such as water and CO2, formed a thick, deep atmosphere surrounding the post-impact Earth. This atmosphere was opaque to thermal radiation, allowing heat to escape to space only at the runaway greenhouse threshold of approximately 100 W m(-2). The duration of this runaway greenhouse stage was limited to approximately 10 Myr by the internal energy and tidal heating, ending with a partially crystalline uppermost mantle and a solid deep mantle. At this point, the crust was able to cool efficiently and solidified at the surface. After the condensation of the water ocean, approximately 100 bar of CO2 remained in the atmosphere, creating a solar-heated greenhouse, while the surface cooled to approximately 500 K. Almost all this CO2 had to be sequestered by subduction into the mantle by 3.8 Ga, when the geological record indicates the presence of life and hence a habitable environment. The deep CO2 sequestration into the mantle could be explained by a rapid subduction of the old oceanic crust, such that the top of the crust would remain cold and retain its CO2. Kinematically, these episodes would be required to have both fast subduction (and hence seafloor spreading) and old crust. Hadean oceanic crust that formed from hot mantle would have been thicker than modern crust, and therefore only old crust underlain by cool mantle lithosphere could subduct. Once subduction started, the basaltic crust would turn into dense eclogite, increasing the rate of subduction. The rapid subduction would stop when the young partially frozen crust from the rapidly spreading ridge entered the subduction zone. © 2014 The Author(s) Published by the Royal Society. All rights reserved.

Water column distribution and carbon isotopic signal of cholesterol, brassicasterol and particulate organic carbon in the Atlantic sector of the Southern Ocean

NASA Astrophysics Data System (ADS)

Cavagna, A.-J.; Dehairs, F.; Bouillon, S.; Woule-Ebongué, V.; Planchon, F.; Delille, B.; Bouloubassi, I.

2013-04-01

The combination of concentrations and δ13C signatures of Particulate Organic Carbon (POC) and sterols provides a powerful approach to study ecological and environmental changes in both the modern and ancient ocean. We applied this tool to study the biogeochemical changes in the modern ocean water column during the BONUS-GoodHope survey (February-March 2008) from Cape Basin to the northern part of the Weddell Gyre. Cholesterol and brassicasterol were chosen as ideal biomarkers of the heterotrophic and autotrophic carbon pools, respectively, because of their ubiquitous and relatively refractory nature. We document depth distributions of concentrations (relative to bulk POC) and δ13C signatures of cholesterol and brassicasterol combined with CO2 aq. surface concentration variation. While the relationship between CO2 aq. and δ13C of bulk POC and biomarkers have been reported by others for the surface water, our data show that this persists in mesopelagic and deep waters, suggesting that δ13C signatures of certain biomarkers in the water column could be applied as proxies for surface water CO2 aq. We observed a general increase in sterol δ13C signatures with depth, which is likely related to a combination of particle size effects, selective feeding on larger cells by zooplankton, and growth rate related effects. Our data suggest a key role of zooplankton fecal aggregates in carbon export for this part of the Southern Ocean (SO). Additionally, in the southern part of the transect south of the Polar Front (PF), the release of sea-ice algae during the ice demise in the Seasonal Ice Zone (SIZ) is hypothesized to influence the isotopic signature of sterols in the open ocean. Overall, the combined use of δ13C values and concentrations measurements of both bulk organic C and specific sterols throughout the water column offers the promising potential to explore the recent history of plankton and the fate of organic matter in the SO.

Partitioning of ocean and land uptake of CO2 as inferred by delta C-13 measurements from the NOAA Climate Monitoring and Diagnostics Laboratory Global Air Sampling Network

NASA Technical Reports Server (NTRS)

Ciais, Philippe; Tans, Pieter P.; White, James W. C.; Trolier, Michael; Francey, Roger J.; Berry, Joe A.; Randall, David R.; Sellers, Piers J.; Collatz, James G.; Schimel, David S.

1995-01-01

Using delta C-13 measurements in atmospheric CO2 from a cooperative global air sampling network, we determined the partitioning of the net uptake of CO2 between ocean and land as a function of latitude and time. The majority of delta C-13 measurements were made at the Institute of Arctic and Alpine Research (INSTAAR) of the University of Colorado. We perform an inverse deconvolution of both CO2 and delta C-13 observations, using a two-dimensional model of atmospheric transport. Also, the discrimination against C-13 by plant photosynthesis, as a function of latitude and time, is calculated from global runs of the simple biosphere (SiB) model. Uncertainty due to the longitudinal structure of the data, which is not represented by the model, is studied through a bootstrap analysis by adding and omitting measurement sites. The resulting error estimates for our inferred sources and sinks are of the order of 1 GTC (1 GTC = 10(exp 15) gC). Such error bars do not reflect potential systematic errors arising from our estimates of the isotopic disequilibria between the atmosphere and the oceans and biosphere, which are estimated in a separate sensitivity analysis. With respect to global totals for 1992 we found that 3.2 GTC of carbon dissolved into the ocean and that 1.5 GTC were sequestered by land ecosystems. Northern hemisphere ocean gyres north of 15 deg N absorbed 2.7 GTC. The equatorial oceans between 10 deg S and 10 deg N were a net source to the atmosphere of 0.9 GTC. We obtained a sink of 1.6 GTC in southern ocean gyres south of 20 deg S, although the deconvolution is poorly constrained by sparse data coverage at high southern latitudes. The seasonal uptake of CO2 in the northern gyres appears to be correlated with a bloom of phytoplankton in surface waters. On land, northern temperate and boreal ecosystems between 35 deg N and 65 deg N were found to be a major sink of CO2 in 1992, as large as 3.5 GTC. Northern tropical ecosystems (equator-30 deg N) appear to be a net source to the source to the atmosphere of 2 GTC which could reflect biomass burning. A small sink, 0.3 GTC, was inferred for southern tropical ecosystems (30 deg S-equator).

Low reservoir ages for the surface ocean from mid-Holocene Florida corals

USGS Publications Warehouse

Druffel, E.R.M.; Robinson, L.F.; Griffin, S.; Halley, R.B.; Southon, J.R.; Adkins, J.F.

2008-01-01

The 14C reservoir age of the surface ocean was determined for two Holocene periods (4908-4955 and 3008-3066 calendar (cal) B.P.) using U/Th-dated corals from Biscayne National Park, Florida, United States. We found that the average reservoir ages for these two time periods (294 ?? 33 and 291 ?? 27 years, respectively) were lower than the average value between A.D. 1600 and 1900 (390 ?? 60 years) from corals. It appears that the surface ocean was closer to isotopic equilibrium with CO2 in the atmosphere during these two time periods than it was during recent times. Seasonal ??18O measurements from the younger coral are similar to modern values, suggesting that mixing with open ocean waters was indeed occurring during this coral's lifetime. Likely explanations for the lower reservoir age include increased stratification of the surface ocean or increased ??14C values of subsurface waters that mix into the surface. Our results imply that a more correct reservoir age correction for radiocarbon measurements of marine samples in this location from the time periods ???3040 and ???4930 cal years B.P. is ???292 ?? 30 years, less than the canonical value of 404 ?? 20 years. Copyright 2008 by the American Geophysical Union.

Integration of an Emerging Highly Sensitive Optical CO2 Sensor for Ocean Monitoring on an Existing Data Acquisition System SeaKeeper 1000 (trademark)

DTIC Science & Technology

2012-09-30

be deployed in geat numbers to autonomously monitor the overall patterns of CO2 emissions and ocean acidification . OBJECTIVES  Meet the...Integration of an Emerging Highly Sensitive Optical CO2 Sensor for Ocean Monitoring on an Existing Data Acquisition System SeaKeeper 1000TM Annual...challenging requirements for ocean pCO2 monitoring using an innovative sensor design based on high sensitivity fluorescence detection.  Assemble the system

Integration of an Emerging Highly Sensitive Optical CO2 Sensor for Ocean Monitoring on an Existing Data Acquisition System SeaKeeper 1000(TM)

DTIC Science & Technology

2011-09-30

be deployed in geat numbers to autonomously monitor the overall patterns of CO2 emissions and ocean acidification . OBJECTIVES  Meet the...Integration of an Emerging Highly Sensitive Optical CO2 Sensor for Ocean Monitoring on an Existing Data Acquisition System SeaKeeper 1000TM Annual...challenging requirements for ocean pCO2 monitoring using an innovative sensor design based on high sensitivity fluorescence detection.  Assemble the system

Carbon and Nutrient Dynamics and Fluxes in the Northwest European Continental Shelf Sea

NASA Astrophysics Data System (ADS)

Humphreys, M. P.; Moore, M. M.; Achterberg, E. P.; Griffiths, A.; Smilenova, A.; Chowdhury, M. Z. H.; Kivimae, C.; Hartman, S. E.; Hopkins, J.; Woodward, M. S.

2016-02-01

Despite covering only about 5 % of the Earth's ocean surface area, shallow marginal seas support 15-20 % of global primary productivity, and are the key interface between the land and the open ocean. They are therefore of critical importance to marine biogeochemical cycles, and may have a significant role in ocean uptake and storage of anthropogenic carbon dioxide (CO2). However, their behaviour is significantly more complex than that of the open ocean, because of the greater heterogeneity of the underlying physical, chemical and biological processes acting upon them. Detailed case-studies of individual regions are therefore essential in order to accurately evaluate their net global influence. The Northwest European continental shelf, in particular the Celtic Sea, was the target of extensive hydrographic sampling from March 2014 to September 2015, as part of the UK Shelf Seas Biogeochemistry research programme (UK-SSB). Here, we use the UK-SSB carbonate chemistry and macronutrient measurements to describe the seasonal biogeochemical cycle in the Celtic Sea. The 100-200 m deep water column proceeds from vertically well mixed in winter to a strongly stratified two-layer structure over spring-summer. The associated seasonal cycle in near-surface biological activity removes dissolved inorganic carbon (DIC) and nutrients, some of which are then exported into the deeper layer. Calculating total inventories of the biogeochemical variables throughout the seasonal cycle, we determine seasonal net CO2 uptake and investigate whether non-Redfieldian macronutrient uptake and remineralisation processes occur. Combining these results with estimated water exchange across the shelf edge further allows us to quantify the strength of the `shelf pump' sink for atmospheric (and anthropogenic) CO2.

A Global 1 Degree by 1 Degree Distribution of Atmospheric/Soil CO2 Consumption by Continental Weathering and of Riverine HCO3 Yield (DB1012)

DOE Data Explorer

Suchet, Philippe Amiotte [Centre National de la Recherche Scientifique, Center de Geochimie de la Surface, Strasbourg Cedex, France; Probst, Jean-Lue [Centre National de la Recherche Scientifique, Center de Geochimie de la Surface, Strasbourg Cedex, France

1995-01-01

The mission of the Centre National de la Recherche Scientifique (CNRS) of Strasbourg Cedex, France is to study "The Global Carbon Cycle and its Perturbation by Man and Climate, the Terrestrial Biosphere". With the support of the Environment Programme of the European Communities, modeling of the spatial distribution of atmospheric-soil CO2 consumption by chemical weathering of continental rocks have been and are being conducted. One of the major results of these studies is a set of global maps which show the distribution of CO2 consumption (FCO2) and the transport of bicarbonate (FHCO3-) from rivers to the ocean, each in moles per kilometer squared per year (mol km2/yr). Continental weathering influences the geologic carbon cycle (Trabalka, 1985). The largest natural exchange fluxes of carbon occur between the atmosphere and the terrestrial biota, and between the atmosphere and the ocean surface waters (Houghton, et. al. 1990). River carbon input to the oceans is a component of the estimate of global air-sea CO2 fluxes (Sarminento and Sundquist 1992). It is estimated that about 0.3 gigatons of carbon per year (GtC/yr) are consumed by the chemical erosion of continental rocks and transferred as HCO3- to the oceans (Berner et. al. 1983; Meybeck 1987; and Probst 1992), while the flux of particulate and dissolved organic carbon transported by rivers to the oceans is estimated to be about 0.4 GtC/yr (Probst 1992). On the whole, about 0.7 GtC/yr are transferred by continental erosion from the soil-biosphere reservoir to the oceans. A model developed by Amiotte Suchet and Probst (1993) calculates the flux of atmospheric-soil CO2 consumed by the chemical erosion of continental rock (i.e., rock weathering) and the bicarbonate river transfer to the ocean. This model is based on a set of empirical relationships between FCO2 and the drainage (runoff) on the major rock types outcropping on the continents. The model assumes that the consumption of atmospheric CO2 by continental weathering is primarily influenced by drainage, and the different types of rocks outcropping the continents. This data base contains estimates of the net flux of atmospheric-soil CO2 (FCO2) produced by the Amiotte Suchet and Probst model and the associated bicarbonate river flux (FHCO3-). These variables are referenced to a 1 degree latitude by 1 degree longitude world grid. The grid contains 64,800 records (i.e. grid cells) originating at -180 degrees West longitude by -90 degrees North latitude, and extending to 180 degrees West longitude by 90 degrees North latitude.

Achieving Negative CO2 Emissions by Protecting Ocean Chemistry

NASA Astrophysics Data System (ADS)

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 combustion power by 2000, per JFK. Brewer says oceans are in "precarious balance". Robust action now gradually restores a safer environment through ocean protection. * "A short history of ocean acidification science in the 20th century", Brewer, MBARI, 2013. ** AAAS Science, Canfield & Kump, 1 Feb. 2013. *** AAAS Science, Mattcr et alia, 10 Jun 2016.

Deep South Atlantic carbonate chemistry and increased interocean deep water exchange during last deglaciation

NASA Astrophysics Data System (ADS)

Yu, Jimin; Anderson, Robert F.; Jin, Zhangdong; Menviel, Laurie; Zhang, Fei; Ryerson, Fredrick J.; Rohling, Eelco J.

2014-04-01

Carbon release from the deep ocean at glacial terminations is a critical component of past climate change, but the underlying mechanisms remain poorly understood. We present a 28,000-year high-resolution record of carbonate ion concentration, a key parameter of the global carbon cycle, at 5-km water depth in the South Atlantic. We observe similar carbonate ion concentrations between the Last Glacial Maximum and the late Holocene, despite elevated concentrations in the glacial surface ocean. This strongly supports the importance of respiratory carbon accumulation in a stratified deep ocean for atmospheric CO2 reduction during the last ice age. After ˜9 μmol/kg decline during Heinrich Stadial 1, deep South Atlantic carbonate ion concentration rose by ˜24 μmol/kg from the onset of Bølling to Pre-boreal, likely caused by strengthening North Atlantic Deep Water formation (Bølling) or increased ventilation in the Southern Ocean (Younger Drays) or both (Pre-boreal). The ˜15 μmol/kg decline in deep water carbonate ion since ˜10 ka is consistent with extraction of alkalinity from seawater by deep-sea CaCO3 compensation and coral reef growth on continental shelves during the Holocene. Between 16,600 and 15,000 years ago, deep South Atlantic carbonate ion values converged with those at 3.4-km water depth in the western equatorial Pacific, as did carbon isotope and radiocarbon values. These observations suggest a period of enhanced lateral exchange of carbon between the deep South Atlantic and Pacific Oceans, probably due to an increased transfer of momentum from southern westerlies to the Southern Ocean. By spreading carbon-rich deep Pacific waters around Antarctica for upwelling, invigorated interocean deep water exchange would lead to more efficient CO2 degassing from the Southern Ocean, and thus to an atmospheric CO2 rise, during the early deglaciation.

Bicarbonate uptake by Southern Ocean phytoplankton

NASA Astrophysics Data System (ADS)

Cassar, Nicolas; Laws, Edward A.; Bidigare, Robert R.; Popp, Brian N.

2004-06-01

Marine phytoplankton have the potential to significantly buffer future increases in atmospheric carbon dioxide levels. However, in order for CO2 fertilization to have an effect on carbon sequestration to the deep ocean, the increase in dissolved CO2 must stimulate primary productivity; that is, marine phototrophs must be CO2 limited [, 1993]. Estimation of the extent of bicarbonate (HCO3-) uptake in the oceans is therefore required to determine whether the anthropogenic carbon sources will enhance carbon flux to the deep ocean. Using short-term 14CO2-disequilibrium experiments during the Southern Ocean Iron Experiment (SOFeX), we show that HCO3- uptake by Southern Ocean phytoplankton is significant. Since the majority of dissolved inorganic carbon (DIC) in the ocean is in the form of bicarbonate, the biological pump may therefore be insensitive to anthropogenic CO2. Approximately half of the DIC uptake observed was attributable to direct HCO3- uptake, the other half being direct CO2 uptake mediated either by passive diffusion or active uptake mechanisms. The increase in growth rates and decrease in CO2 concentration associated with the iron fertilization did not trigger any noticeable changes in the mode of DIC acquisition, indicating that under most environmental conditions the carbon concentrating mechanism (CCM) is constitutive. A low-CO2 treatment induced an increase in uptake of CO2, which we attributed to increased extracellular carbonic anhydrase activity, at the expense of direct HCO3- transport across the plasmalemma. Isotopic disequilibrium experimental results are consistent with Southern Ocean carbon stable isotope fractionation data from this and other studies. Although iron fertilization has been shown to significantly enhance phytoplankton growth and may potentially increase carbon flux to the deep ocean, an important source of the inorganic carbon taken up by phytoplankton in this study was HCO3-, whose concentration is negligibly affected by the anthropogenic rise in CO2. We conclude that biological productivity in this region of the world's ocean is unlikely to be directly regulated by natural or anthropogenic variations in atmospheric CO2 concentrations because of the presence of a constitutive CCM.

Marine Cloud Brightening: regional applications to the weakening of hurricanes and reduction in coral bleaching

NASA Astrophysics Data System (ADS)

Gadian, A.; Hauser, R.; Kleypas, J. A.; Latham, J.; Parkes, B.; Salter, S.

2013-12-01

This study examines the potential to cool ocean surface waters in regions of hurricane genesis and early development. This would be achieved by seeding, with copious quantities of seawater cloud condensation nuclei (CCN), low-level maritime stratocumulus clouds covering these regions or those at the source of incoming currents. Higher cloud droplet density would increase these clouds' reflectivity to incoming sunlight, and possibly their longevity. This approach is a more localized application of the Marine Cloud Brightening (MCB) geoengineering technique promoting global cooling. By utilizing a climate ocean/atmosphere coupled model, HadGEM1, and by judicious seeding of maritime stratocumulus clouds, we demonstrate that we may be able to significantly reduce sea surface temperatures (SSTs) in hurricane development regions. Thus artificial seeding may reduce hurricane intensity; but how well the magnitude of this effect is yet to be determined. Increases in coral bleaching events over the last few decades have been largely caused by rising SSTs, and continued warming is expected to cause even greater increases through this century. Using thr same Global Climate Model to examine the potential of MCB to cool oceanic surface waters in three coral reef provinces. Our simulations indicate that under doubled CO2 conditions, the substantial increases in coral bleaching conditions from current values in three reef regions (Caribbean, French Polynesia, and the Great Barrier Reef) were eliminated when MCB was applied, which reduced the SSTs at these sites roughly to their original values. In this study we also illustrate how even regional application of MCB can affect the planetary meridional heat flux and the reduction in poleward heat transfer. (a) Change in annual average sea surface temperature, Celsius, between the 2xCO2 and CONTROL simulations. (b) Change in annual average sea surface temperature, Celsius, between the CONTROL and 2xCO2+MCB simulations. The dashed black boxes in both panels represent the three coral reef regions. In the Southern north Atlantic, the warmer SSTs in (a) is reduced to the current "control" temperatures, weakening hurricane formation.

Assessing the biogeochemical impact of AMOC collapse during Heinrich Stadial 1: New surface and mid-depth records from the South Atlantic

NASA Astrophysics Data System (ADS)

Lund, D. C.; Lacerra, M.; Schmittner, A.; Yu, J.

2017-12-01

Carbon isotope minima were a ubiquitous feature in the mid-depth (1.5-2.5 km) Atlantic during Heinrich Stadial 1 (HS1, 14.5-17.5 kyr BP), with the most likely driver being a collapse of the Atlantic Meridional Overturning Circulation (AMOC) [1, 2]. Model simulations suggest a weaker AMOC increases the residence time of deep water and causes accumulation of isotopically light respired carbon at mid-depths [3]. Subsequent weakening of the biological pump also causes light carbon to accumulate in the surface ocean and atmosphere, potentially accounting for surface ocean δ13C minima and the initial rise in atmospheric CO2. Here, we test the AMOC hypothesis using high resolution planktonic and benthic δ13C records from the Brazil Margin (1.8 km and 2.1 km water depth). We show that N. dutertrei and G. sacculifer δ13C lags benthic δ13C during HS1 by 500 years. Because the planktonic and benthic results are based on analyses of the same samples, the relative timing is constrained by the stratigraphic offset of the δ13C time series. Our results are consistent with the model prediction of an initial collapse of the AMOC causing δ13C minima at mid-depth followed by weakening of the biological pump and equilibration of the surface ocean with a 13C-depleted atmosphere. We also assess ΣCO2 storage in the mid-depth Atlantic during HS1 using benthic foraminiferal B/Ca as a proxy for [CO32-]. Using replicated high resolution B/Ca records, we show that [CO32-] decreased during HS1, synchronous with apparent weakening of the AMOC. The [CO32-] response is smaller than in the tropical North Atlantic [4], indicating there was a north-south gradient in the [CO32-] signal similar to that for δ13C [5]. The implied ΣCO2 signal is consistent with model results [3], suggesting that carbon is temporarily sequestered in the mid-depth Atlantic during millennial-scale stadial events. We estimate that approximately 75% of the mid-depth δ13C signal was driven by accumulation of remineralized carbon, highlighting the non-conservative nature of δ13C during the last deglaciation. 1 McManus, J. et al. (2004) Nature, 428, 834. 2 Oppo, D. et al. (2015) Paleoceanography, 30, 353. 3 Schmittner, A., & Lund, D. (2015) Clim. Past, 11, 135. 4 Yu, J. et al. (2010) Science, 330 (6007), 1084. 5 Lund, D., et al. (2015) Paleoceanography, 30, 477.

Effects of raised CO2 concentration on the egg production rate and early development of two marine copepods (Acartia steueri and Acartia erythraea).

PubMed

Kurihara, Haruko; Shimode, Shinji; Shirayama, Yoshihisa

2004-11-01

Direct injection of CO(2) into the deep ocean is receiving increasing attention as a way to mitigate increasing atmospheric CO(2) concentration. To assess the potential impact of the environmental change associated with CO(2) sequestration in the ocean, we studied the lethal and sub-lethal effects of raised CO(2) concentration in seawater on adult and early stage embryos of marine planktonic copepods. We found that the reproduction rate and larval development of copepods are very sensitive to increased CO(2) concentration. The hatching rate tended to decrease, and nauplius mortality rate to increase, with increased CO(2) concentration. These results suggest that the marine copepod community will be negatively affected by the disposal of CO(2). This could decrease on the carbon export flux to the deep ocean and change the biological pump. Clearly, further studies are needed to determine whether ocean CO(2) injection is an acceptable strategy to reduce anthropogenic CO(2).

Terrestrial cooling in Northern Europe during the Eocene–Oligocene transition

PubMed Central

Hren, Michael T.; Sheldon, Nathan D.; Grimes, Stephen T.; Collinson, Margaret E.; Hooker, Jerry J.; Bugler, Melanie; Lohmann, Kyger C.

2013-01-01

Geochemical and modeling studies suggest that the transition from the “greenhouse” state of the Late Eocene to the “icehouse” conditions of the Oligocene 34–33.5 Ma was triggered by a reduction of atmospheric pCO2 that enabled the rapid buildup of a permanent ice sheet on the Antarctic continent. Marine records show that the drop in pCO2 during this interval was accompanied by a significant decline in high-latitude sea surface and deep ocean temperature and enhanced seasonality in middle and high latitudes. However, terrestrial records of this climate transition show heterogeneous responses to changing pCO2 and ocean temperatures, with some records showing a significant time lag in the temperature response to declining pCO2. We measured the Δ47 of aragonite shells of the freshwater gastropod Viviparus lentus from the Solent Group, Hampshire Basin, United Kingdom, to reconstruct terrestrial temperature and hydrologic change in the North Atlantic region during the Eocene–Oligocene transition. Our data show a decrease in growing-season surface water temperatures (∼10 °C) during the Eocene–Oligocene transition, corresponding to an average decrease in mean annual air temperature of ∼4–6 °C from the Late Eocene to Early Oligocene. The magnitude of cooling is similar to observed decreases in North Atlantic sea surface temperature over this interval and occurs during major glacial expansion. This suggests a close linkage between atmospheric carbon dioxide concentrations, Northern Hemisphere temperature, and expansion of the Antarctic ice sheets. PMID:23610424

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

NASA Astrophysics Data System (ADS)

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

2018-03-01

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

The impact of transport model differences on CO2 surface flux estimates from OCO-2 retrievals of column average CO2

NASA Astrophysics Data System (ADS)

Basu, Sourish; Baker, David F.; Chevallier, Frédéric; Patra, Prabir K.; Liu, Junjie; Miller, John B.

2018-05-01

We estimate the uncertainty of CO2 flux estimates in atmospheric inversions stemming from differences between different global transport models. Using a set of observing system simulation experiments (OSSEs), we estimate this uncertainty as represented by the spread between five different state-of-the-art global transport models (ACTM, LMDZ, GEOS-Chem, PCTM and TM5), for both traditional in situ CO2 inversions and inversions of XCO2 estimates from the Orbiting Carbon Observatory 2 (OCO-2). We find that, in the absence of relative biases between in situ CO2 and OCO-2 XCO2, OCO-2 estimates of terrestrial flux for TRANSCOM-scale land regions can be more robust to transport model differences than corresponding in situ CO2 inversions. This is due to a combination of the increased spatial coverage of OCO-2 samples and the total column nature of OCO-2 estimates. We separate the two effects by constructing hypothetical in situ networks with the coverage of OCO-2 but with only near-surface samples. We also find that the transport-driven uncertainty in fluxes is comparable between well-sampled northern temperate regions and poorly sampled tropical regions. Furthermore, we find that spatiotemporal differences in sampling, such as between OCO-2 land and ocean soundings, coupled with imperfect transport, can produce differences in flux estimates that are larger than flux uncertainties due to transport model differences. This highlights the need for sampling with as complete a spatial and temporal coverage as possible (e.g., using both land and ocean retrievals together for OCO-2) to minimize the impact of selective sampling. Finally, our annual and monthly estimates of transport-driven uncertainties can be used to evaluate the robustness of conclusions drawn from real OCO-2 and in situ CO2 inversions.

Covariation of deep Southern Ocean oxygenation and atmospheric CO2 through the last ice age.

PubMed

Jaccard, Samuel L; Galbraith, Eric D; Martínez-García, Alfredo; Anderson, Robert F

2016-02-11

No single mechanism can account for the full amplitude of past atmospheric carbon dioxide (CO2) concentration variability over glacial-interglacial cycles. A build-up of carbon in the deep ocean has been shown to have occurred during the Last Glacial Maximum. However, the mechanisms responsible for the release of the deeply sequestered carbon to the atmosphere at deglaciation, and the relative importance of deep ocean sequestration in regulating millennial-timescale variations in atmospheric CO2 concentration before the Last Glacial Maximum, have remained unclear. Here we present sedimentary redox-sensitive trace-metal records from the Antarctic Zone of the Southern Ocean that provide a reconstruction of transient changes in deep ocean oxygenation and, by inference, respired carbon storage throughout the last glacial cycle. Our data suggest that respired carbon was removed from the abyssal Southern Ocean during the Northern Hemisphere cold phases of the deglaciation, when atmospheric CO2 concentration increased rapidly, reflecting--at least in part--a combination of dwindling iron fertilization by dust and enhanced deep ocean ventilation. Furthermore, our records show that the observed covariation between atmospheric CO2 concentration and abyssal Southern Ocean oxygenation was maintained throughout most of the past 80,000 years. This suggests that on millennial timescales deep ocean circulation and iron fertilization in the Southern Ocean played a consistent role in modifying atmospheric CO2 concentration.

The role of Meridional Overturning Circulation (MOC) on Ancient Climates and Implications for Anthropogenic Climate Change

NASA Astrophysics Data System (ADS)

Cumming, M.

2017-12-01

Our increasingly robust history of ancient climates indicates that high latitude glaciation is the ultimate product of an episodic cooling trend that began about 100-million years ago rather than a result of a yet-to-be identified modal change. Antarctic geography (continent surrounded by ocean) allowed ice to develop prior to significant glaciation in the Northern Hemisphere (ocean surrounded by land), but global ice volume generally increased as Earth cooled. The question of what caused the Ice Ages should be reframed as to "What caused the Cenozoic Cooling?" Records tell us that changes in temperature and CO2 levels rise and fall together, however it is not clear when CO2 acts as a driver versus when it is primarily an indicator of temperature change. The episodic nature of the cooling trend suggests other more dynamic phenomena are involved. It is proposed that oceanic meridional overturning circulation (MOC) plays a significant role in regulating Earth's surface temperature. Robust MOC has a cooling effect which results from its sequestration of cold waters (together with their increased heat-absorbing potential) below the surface. Unable to better absorb equatorial insolation for great lengths of time, oceanic deep waters are not able to fully compensate for the heat lost by warm-water transport to Polar Regions. A lag-time between cooling and subsequent warming yields lower operating temperatures commensurate with the strength of global MOC. The long-term decline in global temperatures is largely explained by the tectonic reshaping of ocean basins and the connections between them such that MOC has generally, but not uniformly, increased. Geophysically Influenced MOC (GIMOC) has caused a significant proportion of the lowering of global temperatures in the Cenozoic Era. Short-term disruptions in MOC (and subsequent impacts on global temperatures) were likely involved in Late Pleistocene glacial termination events and may already be compounding present anthropogenic CO2 induced warming.

Eocene cooling linked to early flow across the Tasmanian Gateway.

PubMed

Bijl, Peter K; Bendle, James A P; Bohaty, Steven M; Pross, Jörg; Schouten, Stefan; Tauxe, Lisa; Stickley, Catherine E; McKay, Robert M; Röhl, Ursula; Olney, Matthew; Sluijs, Appy; Escutia, Carlota; Brinkhuis, Henk

2013-06-11

The warmest global temperatures of the past 85 million years occurred during a prolonged greenhouse episode known as the Early Eocene Climatic Optimum (52-50 Ma). The Early Eocene Climatic Optimum terminated with a long-term cooling trend that culminated in continental-scale glaciation of Antarctica from 34 Ma onward. Whereas early studies attributed the Eocene transition from greenhouse to icehouse climates to the tectonic opening of Southern Ocean gateways, more recent investigations invoked a dominant role of declining atmospheric greenhouse gas concentrations (e.g., CO2). However, the scarcity of field data has prevented empirical evaluation of these hypotheses. We present marine microfossil and organic geochemical records spanning the early-to-middle Eocene transition from the Wilkes Land Margin, East Antarctica. Dinoflagellate biogeography and sea surface temperature paleothermometry reveal that the earliest throughflow of a westbound Antarctic Counter Current began ~49-50 Ma through a southern opening of the Tasmanian Gateway. This early opening occurs in conjunction with the simultaneous onset of regional surface water and continental cooling (2-4 °C), evidenced by biomarker- and pollen-based paleothermometry. We interpret that the westbound flowing current flow across the Tasmanian Gateway resulted in cooling of Antarctic surface waters and coasts, which was conveyed to global intermediate waters through invigorated deep convection in southern high latitudes. Although atmospheric CO2 forcing alone would provide a more uniform middle Eocene cooling, the opening of the Tasmanian Gateway better explains Southern Ocean surface water and global deep ocean cooling in the apparent absence of (sub-) equatorial cooling.

Eocene cooling linked to early flow across the Tasmanian Gateway

PubMed Central

Bijl, Peter K.; Bendle, James A. P.; Bohaty, Steven M.; Pross, Jörg; Schouten, Stefan; Tauxe, Lisa; Stickley, Catherine E.; McKay, Robert M.; Röhl, Ursula; Olney, Matthew; Sluijs, Appy; Escutia, Carlota; Brinkhuis, Henk; Klaus, Adam; Fehr, Annick; Williams, Trevor; Carr, Stephanie A.; Dunbar, Robert B.; Gonzàlez, Jhon J.; Hayden, Travis G.; Iwai, Masao; Jimenez-Espejo, Francisco J.; Katsuki, Kota; Kong, Gee Soo; Nakai, Mutsumi; Passchier, Sandra; Pekar, Stephen F.; Riesselman, Christina; Sakai, Toyosaburo; Shrivastava, Prakash K.; Sugisaki, Saiko; Tuo, Shouting; van de Flierdt, Tina; Welsh, Kevin; Yamane, Masako

2013-01-01

The warmest global temperatures of the past 85 million years occurred during a prolonged greenhouse episode known as the Early Eocene Climatic Optimum (52–50 Ma). The Early Eocene Climatic Optimum terminated with a long-term cooling trend that culminated in continental-scale glaciation of Antarctica from 34 Ma onward. Whereas early studies attributed the Eocene transition from greenhouse to icehouse climates to the tectonic opening of Southern Ocean gateways, more recent investigations invoked a dominant role of declining atmospheric greenhouse gas concentrations (e.g., CO2). However, the scarcity of field data has prevented empirical evaluation of these hypotheses. We present marine microfossil and organic geochemical records spanning the early-to-middle Eocene transition from the Wilkes Land Margin, East Antarctica. Dinoflagellate biogeography and sea surface temperature paleothermometry reveal that the earliest throughflow of a westbound Antarctic Counter Current began ∼49–50 Ma through a southern opening of the Tasmanian Gateway. This early opening occurs in conjunction with the simultaneous onset of regional surface water and continental cooling (2–4 °C), evidenced by biomarker- and pollen-based paleothermometry. We interpret that the westbound flowing current flow across the Tasmanian Gateway resulted in cooling of Antarctic surface waters and coasts, which was conveyed to global intermediate waters through invigorated deep convection in southern high latitudes. Although atmospheric CO2 forcing alone would provide a more uniform middle Eocene cooling, the opening of the Tasmanian Gateway better explains Southern Ocean surface water and global deep ocean cooling in the apparent absence of (sub-) equatorial cooling. PMID:23720311

Deglacial Western Equatorial Pacific pCO2 Reconstruction Using Boron Isotopes of Planktonic Foraminiferas

NASA Astrophysics Data System (ADS)

Kubota, K.; Yokoyama, Y.; Ishikawa, T.; Sagawa, T.; Ikehara, M.; Yamazaki, T.

2017-12-01

During the last deglaciation (ca. 19 - 11 ka), partial pressure of CO2 (pCO2) of the atmosphere increased by 80 μatm. Many paleoceanographers point out that the ocean had played an important role in atmospheric CO2 rise, since the ocean have 60 times larger capacity to store carbon compared to the atmosphere. However, evidence on where carbon was transferred from the ocean to the atmosphere is still lacking, hampering our understanding of global carbon cycles in glacial-interglacial timescales. Boron isotope of skeletons of marine calcifying organisms such as corals and foraminiferas can pin down where CO2 source/sink existed, because boron isotopes of marine calcium carbonates is dependent on seawater pH, from which pCO2 of the past seawater can be reconstructed. In previous studies using the boron isotope teqnique, Martinez-Boti et al. (2015, Nature) and Kubota et al. (2014, Scientific Reports) revealed that central and eastern parts of the equatorial Pacific acted as a CO2 source (i.e., CO2 emission) during the last deglaciation, suggesting the equatorial Pacific's contribution to atmospheric CO2 rise. However, some conflicting results have been confirmed in a marine sediment record from the western part of the equatorial Pacific (Palmer & Pearson, 2003, Science), making the conclusion elusive. In this presentation, we will show new results of Mg/Ca, oxygen isotope, and boron isotope measurements during the last 35 ka on two species of surface dwelling foraminiferas (Globigerinoides ruber and G. sacculifer) which was hand-picked separatedly from a well-dated marine sediment core recovered from the West Caroline Basin (KR05-15 PC01) (Yamazaki et al., 2008, GRL). From the new records, we will discuss how the equatorial Pacific behaved during the last deglaciation and how it related to the global carbon cycles.

Does encapsulation protect embryos from the effects of ocean acidification? The example of Crepidula fornicata.

PubMed

Noisette, Fanny; Comtet, Thierry; Legrand, Erwann; Bordeyne, François; Davoult, Dominique; Martin, Sophie

2014-01-01

Early life history stages of marine organisms are generally thought to be more sensitive to environmental stress than adults. Although most marine invertebrates are broadcast spawners, some species are brooders and/or protect their embryos in egg or capsules. Brooding and encapsulation strategies are typically assumed to confer greater safety and protection to embryos, although little is known about the physico-chemical conditions within egg capsules. In the context of ocean acidification, the protective role of encapsulation remains to be investigated. To address this issue, we conducted experiments on the gastropod Crepidula fornicata. This species broods its embryos within capsules located under the female and veliger larvae are released directly into the water column. C. fornicata adults were reared at the current level of CO2 partial pressure (pCO2) (390 μatm) and at elevated levels (750 and 1400 μatm) before and after fertilization and until larval release, such that larval development occurred entirely at a given pCO2. The pCO2 effects on shell morphology, the frequency of abnormalities and mineralization level were investigated on released larvae. Shell length decreased by 6% and shell surface area by 11% at elevated pCO2 (1400 μatm). The percentage of abnormalities was 1.5- to 4-fold higher at 750 μatm and 1400 μatm pCO2, respectively, than at 390 μatm. The intensity of birefringence, used as a proxy for the mineralization level of the larval shell, also decreased with increasing pCO2. These negative results are likely explained by increased intracapsular acidosis due to elevated pCO2 in extracapsular seawater. The encapsulation of C. fornicata embryos did not protect them against the deleterious effects of a predicted pCO2 increase. Nevertheless, C. fornicata larvae seemed less affected than other mollusk species. Further studies are needed to identify the critical points of the life cycle in this species in light of future ocean acidification.

The CarbonTracker Data Assimilation System for CO2 and δ13C (CTDAS-C13 v1.0): retrieving information on land-atmosphere exchange processes

NASA Astrophysics Data System (ADS)

van der Velde, Ivar R.; Miller, John B.; van der Molen, Michiel K.; Tans, Pieter P.; Vaughn, Bruce H.; White, James W. C.; Schaefer, Kevin; Peters, Wouter

2018-01-01

To improve our understanding of the global carbon balance and its representation in terrestrial biosphere models, we present here a first dual-species application of the CarbonTracker Data Assimilation System (CTDAS). The system's modular design allows for assimilating multiple atmospheric trace gases simultaneously to infer exchange fluxes at the Earth surface. In the prototype discussed here, we interpret signals recorded in observed carbon dioxide (CO2) along with observed ratios of its stable isotopologues 13CO2/12CO2 (δ13C). The latter is in particular a valuable tracer to untangle CO2 exchange from land and oceans. Potentially, it can also be used as a proxy for continent-wide drought stress in plants, largely because the ratio of 13CO2 and 12CO2 molecules removed from the atmosphere by plants is dependent on moisture conditions.The dual-species CTDAS system varies the net exchange fluxes of both 13CO2 and CO2 in ocean and terrestrial biosphere models to create an ensemble of 13CO2 and CO2 fluxes that propagates through an atmospheric transport model. Based on differences between observed and simulated 13CO2 and CO2 mole fractions (and thus δ13C) our Bayesian minimization approach solves for weekly adjustments to both net fluxes and isotopic terrestrial discrimination that minimizes the difference between observed and estimated mole fractions.With this system, we are able to estimate changes in terrestrial δ13C exchange on seasonal and continental scales in the Northern Hemisphere where the observational network is most dense. Our results indicate a decrease in stomatal conductance on a continent-wide scale during a severe drought. These changes could only be detected after applying combined atmospheric CO2 and δ13C constraints as done in this work. The additional constraints on surface CO2 exchange from δ13C observations neither affected the estimated carbon fluxes nor compromised our ability to match observed CO2 variations. The prototype presented here can be of great benefit not only to study the global carbon balance but also to potentially function as a data-driven diagnostic to assess multiple leaf-level exchange parameterizations in carbon-climate models that influence the CO2, water, isotope, and energy balance.

Particulate organic matter delta C-13 variations across the Drake Passage

NASA Technical Reports Server (NTRS)

Rau, G. H.; Takahashi, T.; Des Marais, D. J.; Sullivan, C. W.

1991-01-01

Particulate organic matter (POM) was sampled during two cruise transects across the Drake Passage during March 1986 to investigate the unusual C-13 depletion in high-latitude Southern Ocean plankton. This POM delta C-13 transition from -23.2 o/oo at 53.3 deg S to values as low as -30.3 o/oo at above 62 deg S does not track previously reported abrupt changes in water chemistry and plankton species composition associated with the Polar Front Zone. The north-south isotopic trend is not accompanied by significant changes in POM carbon or nitrogen concentrations, or in POM C/N. Differences in plankton standing crop or biochemistry (e.g. lipid content) do not appear responsible for the isotopic trends observed. The latitudinal change in POM delta C-13 is highly correlated with water temperature and with the calculated concentration of CO2 (aq) at equilibrium with atmospheric CO2. These observations are consistent with the hypothesis that CO2 (aq) significantly influences POM delta C-13 in ocean surface waters.

Solar geoengineering, atmospheric water vapor transport, and land plants

NASA Astrophysics Data System (ADS)

Caldeira, Ken; Cao, Long

2015-04-01

This work, using the GeoMIP database supplemented by additional simulations, discusses how solar geoengineering, as projected by the climate models, affects temperature and the hydrological cycle, and how this in turn is related to projected changes in net primary productivity (NPP). Solar geoengineering simulations typically exhibit reduced precipitation. Solar geoengineering reduces precipitation because solar geoengineering reduces evaporation. Evaporation precedes precipitation, and, globally, evaporation equals precipitation. CO2 tends to reduce evaporation through two main mechanisms: (1) CO2 tends to stabilize the atmosphere especially over the ocean, leading to a moister atmospheric boundary layer over the ocean. This moistening of the boundary layer suppresses evaporation. (2) CO2 tends to diminish evapotranspiration, at least in most land-surface models, because higher atmospheric CO2 concentrations allow leaves to close their stomata and avoid water loss. In most high-CO2 simulations, these effects of CO2 which tend to suppress evaporation are masked by the tendency of CO2-warming effect to increase evaporation. In a geoengineering simulation, with the warming effect of CO2 largely offset by the solar geoengineering, the evaporation suppressing characteristics of CO2 are no longer masked and are clearly exhibited. Decreased precipitation in solar geoengineering simulations is a bit like ocean acidification - an effect of high CO2 concentrations that is not offset by solar geoengineering. Locally, precipitation ultimately either evaporates (much of that through the leaves of plants) or runs off through groundwater to streams and rivers. On long time scales, runoff equals precipitation minus evaporation, and thus, water runoff generated at a location is equal to the net atmospheric transport of water to that location. Runoff typically occurs where there is substantial soil moisture, at least seasonally. Locations where there is enough water to maintain runoff are typically locations where there is sufficient water to maintain plant growth. This work aims at: (i) Identifying the geographical distribution of sensitivity of modeled-NPP to changes in CO2, temperature, and various parameters related to the hydrological cycle; (ii) Geographically partitioning changes in modeled-NPP to changes in CO2, temperature, and hydrological variables (and a non-linear interaction term).

Reduced calcification and lack of acclimatization by coral colonies growing in areas of persistent natural acidification.

PubMed

Crook, Elizabeth D; Cohen, Anne L; Rebolledo-Vieyra, Mario; Hernandez, Laura; Paytan, Adina

2013-07-02

As the surface ocean equilibrates with rising atmospheric CO2, the pH of surface seawater is decreasing with potentially negative impacts on coral calcification. A critical question is whether corals will be able to adapt or acclimate to these changes in seawater chemistry. We use high precision CT scanning of skeletal cores of Porites astreoides, an important Caribbean reef-building coral, to show that calcification rates decrease significantly along a natural gradient in pH and aragonite saturation (Ωarag). This decrease is accompanied by an increase in skeletal erosion and predation by boring organisms. The degree of sensitivity to reduced Ωarag measured on our field corals is consistent with that exhibited by the same species in laboratory CO2 manipulation experiments. We conclude that the Porites corals at our field site were not able to acclimatize enough to prevent the impacts of local ocean acidification on their skeletal growth and development, despite spending their entire lifespan in low pH, low Ωarag seawater.

Carbon Cycle Model of a Hawaiian Barrier Reef under Rising Ocean Acidification and Temperature Conditions of the Anthropocene

NASA Astrophysics Data System (ADS)

Drupp, P. S.; Mackenzie, F. T.; De Carlo, E. H.; Guidry, M.

2015-12-01

A CO2-carbonic acid system biogeochemical box model (CRESCAM, Coral Reef and Sediment Carbonate Model) of the barrier reef flat in Kaneohe Bay, Hawai'i was developed to determine how increasing temperature and dissolved inorganic carbon (DIC) content of open ocean source waters, resulting from rising anthropogenic CO2 emissions and ocean acidification, affect the CaCO3budget of coral reef ecosystems. CRESCAM consists of 17 reservoirs and 59 fluxes, including a surface water column domain, a two-layer permeable sediment domain, and a coral framework domain. Physical, chemical, and biological processes such as advection, carbonate precipitation/dissolution, and net ecosystem production and calcification were modeled. The initial model parameters were constrained by experimental and field data from previous coral reef studies, mostly in Kaneohe Bay over the past 50 years. The field studies include data collected by our research group for both the water column and sediment-porewater system.The model system, initially in a quasi-steady state condition estimated for the early 21st century, was perturbed using future projections to the year 2100 of the Anthropocene of atmospheric CO2 ­concentrations, temperature, and source water DIC. These perturbations were derived from the most recent (2013) IPCC's Representative Concentration Pathway (RCP) scenarios, which predict CO2 atmospheric concentrations and temperature anomalies out to 2100. A series of model case studies were also performed whereby one or more parameters (e.g., coral calcification response to declining surface water pH) were altered to investigate potential future outcomes. Our model simulations predict that although the Kaneohe Bay barrier reef will likely see a significant decline in NEC over the coming century, it is unlikely to reach a state of net erosion - a result contrary to several global coral reef model projections. In addition, we show that depending on the future response of NEP and NEC to OA and rising temperatures, the surface waters could switch from being a present-day source of CO2 to the atmosphere to a future sink. This ecosystem specific model can be applied to any reef system where data are available to constrain the initial model state and is a powerful tool for examining future changes in coral reef carbon budgets.

CO2 mitigation via accelerated limestone weathering

USGS Publications Warehouse

Rau, Greg H.; Knauss, Kevin G.; Langer, William H.; Caldeira,

2004-01-01

We evaluate accelerated weathering of limestone (AWL: CO2 + CaCO3 + H2O=> Ca2+ + 2HCO3-) as a low-tech, inexpensive, high-capacity, environmentally-friendly CO2 capture and sequestration technology. With access to seawater and limestone being essential to this approach, significant limestone resources are close to most CO2-emitting power plants along the coastal US. Waste fines, representing more than 20% of current US crushed limestone production (>109 tonnes/yr), could be used as an inexpensive source of AWL carbonate. Under such circumstances CO2 mitigation cost could be as low as $3-$4/tonne. More broadly, 10-20% of US point-source CO2 emissions could be treated at $20-$30/tonne CO2. AWL end-solution disposal in the ocean would significantly reduce effects on ocean pH and carbonate chemistry relative to those caused by direct atmospheric or ocean CO2 disposal. Indeed, the increase in ocean Ca2+ and bicarbonate offered by AWL should enhance growth of corals and other calcifying marine organisms.

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

PubMed Central

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

2015-01-01

Reduced surface–deep ocean exchange and enhanced nutrient consumption by phytoplankton in the Southern Ocean have been linked to lower glacial atmospheric CO2. However, identification of the biological and physical conditions involved and the related processes remains incomplete. Here we specify Southern Ocean surface–subsurface contrasts using a new tool, the combined oxygen and silicon isotope measurement of diatom and radiolarian opal, in combination with numerical simulations. Our data do not indicate a permanent glacial halocline related to melt water from icebergs. Corroborated by numerical simulations, we find that glacial surface stratification was variable and linked to seasonal sea-ice changes. During glacial spring–summer, the mixed layer was relatively shallow, while deeper mixing occurred during fall–winter, allowing for surface-ocean refueling with nutrients from the deep reservoir, which was potentially richer in nutrients than today. This generated specific carbon and opal export regimes turning the glacial seasonal sea-ice zone into a carbon sink. PMID:26382319

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

Storage of respired carbon in the deep ocean may play a significant role in lowering atmospheric CO2 concentrations by about 80 ppm during the last glacial maximum compared to pre-industrial times. The cause of this sequestration and the subsequent release of the deep respired carbon pool at the last termination remains elusive. Within the last glacial period, on millennial timescales, the relationship between the CO2 cycle and any waxing and waning of a deep respired pool also remains unclear. To further our understanding of the millennial variability in the storage of a deep-ocean respired carbon pool during the last glacial, we measure authigenic uranium and 230Th-derived non-lithogenic barium fluxes (xsBa flux) in two high-sedimentation-rate cores from the Panama Basin of the Eastern Equatorial Pacific (EEP) (8JC, 6° 14.0' N, 86° 02.6' W; 1993 m water depth; 17JC 00° 10.8' S, 85° 52.0' W; 2846 m water depth). Sediment authigenic U concentrations are controlled by the redox state of sediments which, in turn, is a function of the rain of organic material from the surface ocean and the oxygen content of bottom waters. At both 8JC and 17JC, the mismatch between xsBa fluxes, a proxy for the reconstruction of oceanic productivity, and authigenic uranium concentrations suggests that the primary control of the latter values is changes in bottom water oxygenation. Peak authigenic uranium concentrations occur during glacial periods MIS 2, 3, and 4, respectively, and are two to three times higher than those during interglacial periods, MIS 1 and 5. EEP bottom waters were likely suboxic during times of the last glacial period when atmospheric CO2 concentrations were at their lowest concentrations. In addition, the pattern of increased deep-water oxygenation during times of higher CO2 during the last glacial is similar to that reported in a study of authigenic U in sediments from the Antarctic Zone of the Southern Ocean (Jaccard et al., 2016). We suggest that a respired carbon pool existed within a large swath of the abyssal Southern and Pacific Oceans throughout the entire last glacial cycle, and that this respired carbon was periodically released through increased ventilation of deep ocean waters. Jaccard et al. (2016) Nature 530, 207-210.

Evolution of Summer Ocean Mixed Layer Heat Content and Ocean/Ice Fluxes in the Arctic Ocean During the Last Decade

NASA Astrophysics Data System (ADS)

Stanton, T. P.; Shaw, W. J.

2014-12-01

Since 2002, a series of 28 Autonomous Ocean Flux Buoys have been deployed in the Beaufort Sea and from the North Pole Environmental Observatory. These long-term ice-deployed instrument systems primarily measure vertical turbulent fluxes of heat, salt and momentum at a depth of 2 - 6 m below the ocean/ice interface, while concurrently measuring current profile every 2m down to approximately 40-50m depth, within the seasonal pycnocline. Additional sensors have been added to measure local ice melt rates acoustically, and finescale thermal structure from the eddy correlation flux sensor up into the ice to resolve summer near-surface heating. The AOFB buoys have typically been co-located with Ice Tethered Profilers, that measure the upper ocean T/S structure and ice mass balance instruments. Comparisons of near-surface heat fluxes, heat content and vertical structure over the last decade will be made for buoys in the Beaufort Sea and Transpolar Drift between the North Pole and Spitzbergen. The effects of enhanced basal melting from ice/albedo feedbacks can be clearly seen in the low ice concentration summer conditions found more recently in the Beaufort Sea, while there are less pronounced effects of enhanced summer surface heating in the higher ice concentrations still found in the transpolar drift.

The Wave Glider°: A New Autonomous Surface Vehicle to Augment MBARI's Growing Fleet of Ocean Observing Systems

NASA Astrophysics Data System (ADS)

Tougher, B. B.

2011-12-01

Monterey Bay Aquarium Research Institute's (MBARI) evolving fleet of ocean observing systems has made it possible to collect information and data about a wide variety of ocean parameters, enabling researchers to better understand marine ecosystems. In collaboration with Liquid Robotics Inc, the designer of the Wave Glider autonomous surface vehicle (ASV), MBARI is adding a new capability to its suite of ocean observing tools. This new technology will augment MBARI research programs that use satellites, ships, moorings, drifters, autonomous underwater vehicles (AUVs) and remotely operated vehicles (ROVs) to improve data collection of temporally and spatially variable oceanographic features. The Wave Glider ASV derives its propulsion from wave energy, while sensors and communications are powered through the use of two solar panels and batteries, enabling it to remain at sea indefinitely. Wave Gliders are remotely controlled via real-time Iridium burst communications, which also permit real-time data telemetry. MBARI has developed Ocean Acidification (OA) moorings to continuously monitor the chemical and physical changes occurring in the ocean as a result of increased levels of atmospheric carbon dioxide (CO2). The moorings are spatially restricted by being anchored to the seafloor, so during the summer of 2011 the ocean acidification sensor suite designed for moorings was integrated into a Wave Glider ASV to increase both temporal and spatial ocean observation capabilities. The OA sensor package enables the measurement of parameters essential to better understanding the changing acidity of the ocean, specifically pCO2, pH, oxygen, salinity and temperature. The Wave Glider will also be equipped with a meteorological sensor suite that will measure air temperature, air pressure, and wind speed and direction. The OA sensor integration into a Wave Glider was part of MBARI's 2011 summer internship program. This project involved designing a new layout for the OA sensors within a Wave Glider aft payload dry box. The Wave Glider OA sensor suite includes the addition of a pCO2 standard tank not included within the current OA moorings. Communication links between MBARI electronics and Liquid Robotics Control and Communications were successfully established in the laboratory, however further steps to fully integrate and test the OA system into a Wave Glider ASV are still needed. In the future these ASVs will provide platforms for additional surface and subsurface instrumentation, particularly with MBARI's upcoming Controlled, Agile, and Novel, Observing Network (CANON) projects. The integration of the OA sensor package into a Wave Glider ASV will make it possible to continuously monitor the marine environment during adverse weather conditions which are often difficult to document but scientifically important.

Plate tectonics, habitability and life

NASA Astrophysics Data System (ADS)

Spohn, Tilman; Breuer, Doris

2016-04-01

The role of plate tectonics in defining habitability of terrestrial planets is being increasingly discussed (e.g., Elkins-Tanton, 2015). Plate tectonics is a significantly evolved concept with a large variety of aspects. In the present context, cycling of material between near surface and mantle reservoirs is most important. But increased heat transport through mixing of cold lithosphere with the deep interior and formation of continental crust may also matter. An alternative mechanism of material cycling between these reservoirs is hot-spot volcanism combined with crust delamination. Hot-spot volcanism will transport volatiles to the atmosphere while delamination will mix crust, possibly altered by sedimentation and chemical reactions, with the mantle. The mechanism works as long as the stagnant lithosphere plate has not grown thicker than the crust and as long as volcanic material is added onto the crust. Thermal evolution studies suggest that the mechanism could work for the first 1-2 Ga of planetary evolution. The efficiency of the mechanism is limited by the ratio of extrusive to intrusive volcanism, which is thought to be less than 0.25. Plate tectonics would certainly have an advantage by working even for more evolved planets. A simple, most-used concept of habitability requires the thermodynamic stability of liquid water on the surface of a planet. Cycling of CO2between the atmosphere, oceans and interior through subduction and surface volcanism is an important element of the carbonate-silicate cycle, a thermostat feedback cycle that will keep the atmosphere from entering into a runaway greenhouse. Calculations for a model Earth lacking plate tectonics but degassing CO2, N, and H2O to form a surface ocean and a secondary atmosphere (Tosi et al, 2016) suggest that liquid water can be maintained on the surface for 4.5Ga. The model planet would then qualify as habitable. It is conceivable that the CO2 buffering capability of its ocean together with silicate weathering of possible land surfaces and a biosphere could set up a CO2 sink that would further stabilize the temperature. As long as the planet keeps degassing CO2 at a sufficient rate, CO2 recycling through the mantle may not be required. However, this would require a sufficiently oxidized planet early on. If not sufficiently oxidized during accretion and core formation, oxidization of the planet would require cycling of matter between surface and interior reservoirs. Oxidization of an initially reduced Earth interior with the help of plate tectonics has been cited as a possible mechanism to allow the building up of oxygen in the terrestrial atmosphere around 2.3Ga b.p. (e.g., Catling and Claire, 2005), a pre-requisite for more evolved eukaryotic life. The oxidization would diminish a sink in the oxygen budget of the atmosphere by lowering the rate of outgassing of chemically reducing gases from the interior. Clearly, plate tectonics is a mechanism more potent of keeping a planet habitable and allow evolution of the biosphere than alternative concepts such as crust delamination. Catling, DC, Claire DW (2005), EPSL, 237, 1-20 Elkins-Tanton, L (2015) AGU Fall Meeting Abstract Tosi, N et al. (2016) EGU Abstract

Quantifying the influence of CO2 seasonality on future aragonite undersaturation onset

NASA Astrophysics Data System (ADS)

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

2015-10-01

Ocean acidification is a predictable consequence of rising atmospheric carbon dioxide (CO2), and is highly likely to impact the entire marine ecosystem - from plankton at the base of the food chain to fish at the top. Factors which are expected to be impacted include reproductive health, organism growth and species composition and distribution. Predicting when critical threshold values will be reached is crucial for projecting the future health of marine ecosystems and for marine resources planning and management. The impacts of ocean acidification will be first felt at the seasonal scale, however our understanding how seasonal variability will influence rates of future ocean acidification remains poorly constrained due to current model and data limitations. To address this issue, we first quantified the seasonal cycle of aragonite saturation state utilizing new data-based estimates of global ocean-surface dissolved inorganic carbon and alkalinity. This seasonality was then combined with earth system model projections under different emissions scenarios (representative concentration pathways; RCPs 2.6, 4.5 and 8.5) to provide new insights into future aragonite undersaturation onset. Under a high emissions scenario (RCP 8.5), our results suggest accounting for seasonality will bring forward the initial onset of month-long undersaturation by 17 ± 10 years compared to annual-mean estimates, with differences extending up to 35 ± 16 years in the North Pacific due to strong regional seasonality. This earlier onset will result in large-scale undersaturation once atmospheric CO2 reaches 496 ppm in the North Pacific and 511 ppm in the Southern Ocean, independent of emission scenario. This work suggests accounting for seasonality is critical to projecting the future impacts of ocean acidification on the marine environment.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Shen, W.; Tuleya, R.E.; Ginis, I.

In this study, the effect of thermodynamic environmental changes on hurricane intensity is extensively investigated with the National Oceanic and Atmospheric Administration Geophysical Fluid Dynamics Laboratory hurricane model for a suite of experiments with different initial upper-tropospheric temperature anomalies up to {+-}4 C and sea surface temperatures ranging from 26 to 31 C given the same relative humidity profile. The results indicate that stabilization in the environmental atmosphere and sea surface temperature (SST) increase cause opposing effects on hurricane intensity. The offsetting relationship between the effects of atmospheric stability increase (decrease) and SST increase (decrease) is monotonic and systematic inmore » the parameter space. This implies that hurricane intensity increase due to a possible global warming associated with increased CO{sub 2} is considerably smaller than that expected from warming of the oceanic waters alone. The results also indicate that the intensity of stronger (weaker) hurricanes is more (less) sensitive to atmospheric stability and SST changes. The model-attained hurricane intensity is found to be well correlated with the maximum surface evaporation and the large-scale environmental convective available potential energy. The model-attained hurricane intensity if highly correlated with the energy available from wet-adiabatic ascent near the eyewall relative to a reference sounding in the undisturbed environment for all the experiments. Coupled hurricane-ocean experiments show that hurricane intensity becomes less sensitive to atmospheric stability and SST changes since the ocean coupling causes larger (smaller) intensity reduction for stronger (weaker) hurricanes. This implies less increase of hurricane intensity related to a possible global warming due to increased CO{sub 2}.« less

Low pH Springs - A Natural Laboratory for Ocean Acidification

NASA Astrophysics Data System (ADS)

Derse, E.; Rebolledo-Vieyra, M.; Potts, D. C.; Paytan, A.

2009-12-01

Recent increases in atmospheric carbon dioxide of 40% above pre-industrial levels has resulted in rising aqueous CO2 concentrations that lower the pH of the oceans. Currently, the surface ocean has an average pH between 8.1 and 8.2: it is estimated that over the next 100 years this value will decrease by ~0.4 pH units. Previous studies have highlighted the negative impacts that changes in pH (and the resulting CaCO3 saturation state) have on marine organisms; however, to date, very little is known about the long-term impacts of ocean acidification on ecosystems as a whole. The Yucatán Peninsula of Quintana Roo, Mexico, represents an ecosystem where naturally low pH groundwater (7.25-8.07) has been discharging offshore at highly localized points (called ojos) since the last deglaciation. We present preliminary chemical and biological data on a selection of ojos from lagoon sites in Puerto Morelos, Mexico. We address the potential long-term implications of low pH waters on marine ecosystems.

Nutrient co-limited Trichodesmium as nitrogen source or sink in a future ocean.

PubMed

Walworth, Nathan G; Fu, Fei-Xue; Lee, Michael D; Cai, Xiaoni; Saito, Mak A; Webb, Eric A; Hutchins, David A

2017-11-27

Nitrogen-fixing (N 2 ) cyanobacteria provide bioavailable nitrogen to vast ocean regions but are in turn limited by iron (Fe) and/or phosphorus (P), which may force them to employ alternative nitrogen acquisition strategies. The adaptive responses of nitrogen-fixers to global-change drivers under nutrient-limited conditions could profoundly alter the current ocean nitrogen and carbon cycles. Here, we show that the globally-important N 2 -fixer Trichodesmium fundamentally shifts nitrogen metabolism towards organic-nitrogen scavenging following long-term high-CO 2 adaptation under iron and/or phosphorus (co)-limitation. Global shifts in transcripts and proteins under high CO 2 /Fe-limited and/or P-limited conditions include decreases in the N 2 -fixing nitrogenase enzyme, coupled with major increases in enzymes that oxidize trimethylamine (TMA). TMA is an abundant, biogeochemically-important organic nitrogen compound that supports rapid Trichodesmium growth while inhibiting N 2 fixation. In a future high-CO 2 ocean, this whole-cell energetic reallocation towards organic nitrogen scavenging and away from N 2 -fixation may reduce new-nitrogen inputs by Trichodesmium , while simultaneously depleting the scarce fixed-nitrogen supplies of nitrogen-limited open ocean ecosystems. Importance Trichodesmium is among the most biogeochemically-significant microorganisms in the ocean, since it supplies up to 50% of the new nitrogen supporting open ocean food webs. We used Trichodesmium cultures adapted to high CO 2 for 7 years followed by additional exposure to iron and/or phosphorus (co)-limitation. We show that 'future ocean' conditions of high CO 2 and concurrent nutrient limitation(s) fundamentally shift nitrogen metabolism away from nitrogen fixation, and instead towards upregulation of organic-nitrogen scavenging pathways. We show that Trichodesmium's responses to projected future ocean conditions include decreases in the nitrogen-fixing nitrogenase enzymes, coupled with major increases in enzymes that oxidize the abundant organic nitrogen source trimethylamine (TMA). Such a shift towards organic nitrogen uptake and away from nitrogen fixation may substantially reduce new-nitrogen inputs by Trichodesmium to the rest of the microbial community in the future high-CO 2 ocean, with potential global implications for ocean carbon and nitrogen cycling. Copyright © 2017 American Society for Microbiology.

The southeastern continental shelf of the United States as an atmospheric CO 2 source and an exporter of inorganic carbon to the ocean

NASA Astrophysics Data System (ADS)

Aleck Wang, Zhaohui; Cai, Wei-Jun; Wang, Yongchen; Ji, Hongwei

2005-10-01

The US southeastern continental shelf, also known as the South Atlantic Bight (SAB), is a strong source of CO 2 to the atmosphere, which is in direct contrast to recent reports regarding other major continental shelves. Both spatial (cross-shelf) and seasonal variations of the CO 2 system were pronounced in the SAB. Sea surface pCO 2 in winter was undersaturated relative to the atmosphere, while oversaturation of pCO 2 dominated the entire shelf water in all other seasons. Annually, the SAB releases CO 2 to the atmosphere at an average rate of 30 g C m -2 (2.5 mol C m -2). This system also discharges dissolved inorganic carbon to the open ocean (30 g C m -2 yr -1). Methods of estimating CO 2 flux and DIC flux are critically evaluated and compared. A carbon mass balance model in the SAB is presented based on inorganic carbon fluxes from this study and organic carbon fluxes from literature. The carbon budget is much closer to balance by using this carbon flux approach than by direct measurements of primary production and respiration. It is concluded that the SAB is a net heterotrophic system annually. Intensified heating, elevated input of inorganic carbon from coastal salt marshes, microbial respiration of marsh-exported organic carbon and the lack of annual spring blooms all contribute to maintaining the SAB as a strong CO 2 source to the atmosphere during the warm seasons. In winter, the primary factor that governs the CO 2 sink in the SAB is likely the cooling process. Strong heterotrophy during warm seasons also sustains the SAB to be an exporter of inorganic carbon to the open ocean annually. The SAB shelf functions differently from the East China Sea, the North Atlantic European Shelves, and the Mid-Atlantic Bight as a source or sink of atmospheric CO 2. The SAB is classified as a "marsh-dominated" shelf as compared to other shelves in terms of carbon dynamics. Further work to study carbon dynamics in coastal margins is warranted to interpret their roles in the global CO 2 budget.

CO2-induced ocean acidification increases anxiety in Rockfish via alteration of GABAA receptor functioning

PubMed Central

Hamilton, Trevor James; Holcombe, Adam; Tresguerres, Martin

2014-01-01

The average surface pH of the ocean is dropping at a rapid rate due to the dissolution of anthropogenic CO2, raising concerns for marine life. Additionally, some coastal areas periodically experience upwelling of CO2-enriched water with reduced pH. Previous research has demonstrated ocean acidification (OA)-induced changes in behavioural and sensory systems including olfaction, which is due to altered function of neural gamma-aminobutyric acid type A (GABAA) receptors. Here, we used a camera-based tracking software system to examine whether OA-dependent changes in GABAA receptors affect anxiety in juvenile Californian rockfish (Sebastes diploproa). Anxiety was estimated using behavioural tests that measure light/dark preference (scototaxis) and proximity to an object. After one week in OA conditions projected for the next century in the California shore (1125 ± 100 µatm, pH 7.75), anxiety was significantly increased relative to controls (483 ± 40 µatm CO2, pH 8.1). The GABAA-receptor agonist muscimol, but not the antagonist gabazine, caused a significant increase in anxiety consistent with altered Cl− flux in OA-exposed fish. OA-exposed fish remained more anxious even after 7 days back in control seawater; however, they resumed their normal behaviour by day 12. These results show that OA could severely alter rockfish behaviour; however, this effect is reversible. PMID:24285203

CO2-induced ocean acidification increases anxiety in rockfish via alteration of GABAA receptor functioning.

PubMed

Hamilton, Trevor James; Holcombe, Adam; Tresguerres, Martin

2014-01-22

The average surface pH of the ocean is dropping at a rapid rate due to the dissolution of anthropogenic CO2, raising concerns for marine life. Additionally, some coastal areas periodically experience upwelling of CO2-enriched water with reduced pH. Previous research has demonstrated ocean acidification (OA)-induced changes in behavioural and sensory systems including olfaction, which is due to altered function of neural gamma-aminobutyric acid type A (GABAA) receptors. Here, we used a camera-based tracking software system to examine whether OA-dependent changes in GABAA receptors affect anxiety in juvenile Californian rockfish (Sebastes diploproa). Anxiety was estimated using behavioural tests that measure light/dark preference (scototaxis) and proximity to an object. After one week in OA conditions projected for the next century in the California shore (1125 ± 100 µatm, pH 7.75), anxiety was significantly increased relative to controls (483 ± 40 µatm CO2, pH 8.1). The GABAA-receptor agonist muscimol, but not the antagonist gabazine, caused a significant increase in anxiety consistent with altered Cl(-) flux in OA-exposed fish. OA-exposed fish remained more anxious even after 7 days back in control seawater; however, they resumed their normal behaviour by day 12. These results show that OA could severely alter rockfish behaviour; however, this effect is reversible.

Host-associated coral reef microbes respond to the cumulative pressures of ocean warming and ocean acidification.

PubMed

Webster, N S; Negri, A P; Botté, E S; Laffy, P W; Flores, F; Noonan, S; Schmidt, C; Uthicke, S

2016-01-13

Key calcifying reef taxa are currently threatened by thermal stress associated with elevated sea surface temperatures (SST) and reduced calcification linked to ocean acidification (OA). Here we undertook an 8 week experimental exposure to near-future climate change conditions and explored the microbiome response of the corals Acropora millepora and Seriatopora hystrix, the crustose coralline algae Hydrolithon onkodes, the foraminifera Marginopora vertebralis and Heterostegina depressa and the sea urchin Echinometra sp. Microbial communities of all taxa were tolerant of elevated pCO2/reduced pH, exhibiting stable microbial communities between pH 8.1 (pCO2 479-499 μatm) and pH 7.9 (pCO2 738-835 μatm). In contrast, microbial communities of the CCA and foraminifera were sensitive to elevated seawater temperature, with a significant microbial shift involving loss of specific taxa and appearance of novel microbial groups occurring between 28 and 31 °C. An interactive effect between stressors was also identified, with distinct communities developing under different pCO2 conditions only evident at 31 °C. Microbiome analysis of key calcifying coral reef species under near-future climate conditions highlights the importance of assessing impacts from both increased SST and OA, as combinations of these global stressors can amplify microbial shifts which may have concomitant impacts for coral reef structure and function.

Relationship between synoptic scale weather systems and column averaged atmospheric CO2

NASA Astrophysics Data System (ADS)

Naja, M.; Yaremchuk, A.; Onishi, R.; Maksyutov, S.; Inoue, G.

2005-12-01

Analysis of the atmospheric CO2 observations with transport models contributes to the understanding of the geographical distributions of CO2 sources and sinks. Space-borne sensors could be advantageous for CO2 measurements as they can provide wider spatial and temporal coverage. Inversion studies have suggested requirement of better than 1% precision for the space-borne observations. Since sources and sinks are inferred from spatial and temporal gradients in CO2, the space-borne observations must have no significant geographically varying biases. To study the dynamical biases in column CO2 due to possible correlation between clouds and atmospheric CO2 at synoptic scale, we have made simulations of CO2 (1988-2003) using NIES tracer transport model. Model resolution is 2.5o x 2.5o in horizontal and it has 15 vertical sigma-layers. Fluxes for (1) fossil fuels, (2) terrestrial biosphere (CASA NEP), (3) the oceans, and (4) inverse model derived monthly regional fluxes from 11 land and 11 ocean regions are used. SVD truncation is used to filter out noise in the inverse model flux time series. Model reproduces fairly well CO2 global trend and observed time series at monitoring sites around the globe. Lower column CO2 concentration is simulated inside cyclonic systems in summer over North hemispheric continental areas. Surface pressure is used as a proxy for dynamics and it is demonstrated that anomalies in column averaged CO2 has fairly good correlation with the anomalies in surface pressure. Positive correlation, as high as 0.7, has been estimated over parts of Siberia and N. America in summer time. Our explanation is based on that the low-pressure system is associated the upward motion, which leads to lower column CO2 values over these regions due to lifting of CO2-depleted summertime PBL air, and higher column CO2 over source areas. A sensitivity study without inverse model fluxes shows same correlation. The low-pressure systems' induced negative biases are 0.4-0.6 ppmv in summer over Siberia. Therefore it is essential to consider this bias due to covariance with vertical motion, while analyzing the column CO2 from space-borne observations together with in-situ observations, because most optical observations are not available under cloudy conditions typical for the low-pressure system.

Atmospheric Carbon Dioxide and the Global Carbon Cycle: The Key Uncertainties

DOE R&D Accomplishments Database

Peng, T. H.; Post, W. M.; DeAngelis, D. L.; Dale, V. H.; Farrell, M. P.

1987-12-01

The biogeochemical cycling of carbon between its sources and sinks determines the rate of increase in atmospheric CO{sub 2} concentrations. The observed increase in atmospheric CO{sub 2} content is less than the estimated release from fossil fuel consumption and deforestation. This discrepancy can be explained by interactions between the atmosphere and other global carbon reservoirs such as the oceans, and the terrestrial biosphere including soils. Undoubtedly, the oceans have been the most important sinks for CO{sub 2} produced by man. But, the physical, chemical, and biological processes of oceans are complex and, therefore, credible estimates of CO{sub 2} uptake can probably only come from mathematical models. Unfortunately, one- and two-dimensional ocean models do not allow for enough CO{sub 2} uptake to accurately account for known releases. Thus, they produce higher concentrations of atmospheric CO{sub 2} than was historically the case. More complex three-dimensional models, while currently being developed, may make better use of existing tracer data than do one- and two-dimensional models and will also incorporate climate feedback effects to provide a more realistic view of ocean dynamics and CO{sub 2} fluxes. The instability of current models to estimate accurately oceanic uptake of CO{sub 2} creates one of the key uncertainties in predictions of atmospheric CO{sub 2} increases and climate responses over the next 100 to 200 years.

Chemical and biological impacts of ocean acidification along the west coast of North America

NASA Astrophysics Data System (ADS)

Feely, Richard A.; Alin, Simone R.; Carter, Brendan; Bednaršek, Nina; Hales, Burke; Chan, Francis; Hill, Tessa M.; Gaylord, Brian; Sanford, Eric; Byrne, Robert H.; Sabine, Christopher L.; Greeley, Dana; Juranek, Lauren

2016-12-01

The continental shelf region off the west coast of North America is seasonally exposed to water with a low aragonite saturation state by coastal upwelling of CO2-rich waters. To date, the spatial and temporal distribution of anthropogenic CO2 (Canth) within the CO2-rich waters is largely unknown. Here we adapt the multiple linear regression approach to utilize the GO-SHIP Repeat Hydrography data from the northeast Pacific to establish an annually updated relationship between Canth and potential density. This relationship was then used with the NOAA Ocean Acidification Program West Coast Ocean Acidification (WCOA) cruise data sets from 2007, 2011, 2012, and 2013 to determine the spatial variations of Canth in the upwelled water. Our results show large spatial differences in Canth in surface waters along the coast, with the lowest values (37-55 μmol kg-1) in strong upwelling regions off southern Oregon and northern California and higher values (51-63 μmol kg-1) to the north and south of this region. Coastal dissolved inorganic carbon concentrations are also elevated due to a natural remineralized component (Cbio), which represents carbon accumulated through net respiration in the seawater that has not yet degassed to the atmosphere. Average surface Canth is almost twice the surface remineralized component. In contrast, Canth is only about one third and one fifth of the remineralized component at 50 m and 100 m depth, respectively. Uptake of Canth has caused the aragonite saturation horizon to shoal by approximately 30-50 m since the preindustrial period so that undersaturated waters are well within the regions of the continental shelf that affect the shell dissolution of living pteropods. Our data show that the most severe biological impacts occur in the nearshore waters, where corrosive waters are closest to the surface. Since the pre-industrial times, pteropod shell dissolution has, on average, increased approximately 19-26% in both nearshore and offshore waters.

The impact of seawater saturation state and bicarbonate ion concentration on calcification by new recruits of two Atlantic corals

NASA Astrophysics Data System (ADS)

de Putron, S. J.; McCorkle, D. C.; Cohen, A. L.; Dillon, A. B.

2011-06-01

Rising concentrations of atmospheric CO2 are changing the carbonate chemistry of the oceans, a process known as ocean acidification (OA). Absorption of this CO2 by the surface oceans is increasing the amount of total dissolved inorganic carbon (DIC) and bicarbonate ion (HCO3 -) available for marine calcification yet is simultaneously lowering the seawater pH and carbonate ion concentration ([CO3 2-]), and thus the saturation state of seawater with respect to aragonite (Ωar). We investigated the relative importance of [HCO3 -] versus [CO3 2-] for early calcification by new recruits (primary polyps settled from zooxanthellate larvae) of two tropical coral species, Favia fragum and Porites astreoides. The polyps were reared over a range of Ωar values, which were manipulated by both acid-addition at constant pCO2 (decreased total [HCO3 -] and [CO3 2-]) and by pCO2 elevation at constant alkalinity (increased [HCO3 -], decreased [CO3 2-]). Calcification after 2 weeks was quantified by weighing the complete skeleton (corallite) accreted by each polyp over the course of the experiment. Both species exhibited the same negative response to decreasing [CO3 2-] whether Ωar was lowered by acid-addition or by pCO2 elevation—calcification did not follow total DIC or [HCO3 -]. Nevertheless, the calcification response to decreasing [CO3 2-] was nonlinear. A statistically significant decrease in calcification was only detected between Ωar = <2.5 and Ωar = 1.1-1.5, where calcification of new recruits was reduced by 22-37% per 1.0 decrease in Ωar. Our results differ from many previous studies that report a linear coral calcification response to OA, and from those showing that calcification increases with increasing [HCO3 -]. Clearly, the coral calcification response to OA is variable and complex. A deeper understanding of the biomineralization mechanisms and environmental conditions underlying these variable responses is needed to support informed predictions about future OA impacts on corals and coral reefs.

Temperature correlations between the eastern equatorial Pacific and Antarctica over the past 230,000 years

NASA Astrophysics Data System (ADS)

Koutavas, Athanasios

2018-03-01

Tropical sea surface temperatures (SSTs) warmed and cooled in step with the Pleistocene ice age cycles, but the mechanisms are not known. It is assumed that the answer must involve radiative forcing by CO2 but SST reconstructions have been too sparse for a conclusive test. Here I present a 230,000-yr tropical SST stack from the eastern equatorial Pacific (EEP) using two new Mg/Ca reconstructions combined with three earlier ones. The EEP stack shows persistent covariation with Antarctic temperature on orbital and millennial timescales indicating tight coupling between the two regions. This coupling however cannot be explained solely by CO2 forcing because in at least one important case, the Marine Isotope Stage (MIS) 5e-5d glacial inception, both regions cooled ∼5-6.5 thousand years before CO2 decreased. More likely, their covariation was due to advection of Antarctic climate signals to the EEP by the ocean. To explain the MIS 5e-5d event and glacial inception in general the hypothesis is advanced that the cooling signal spreads globally from the Northern Hemisphere with an active ocean circulation - first from the North Atlantic to the Southern Ocean with a colder North Atlantic Deep Water, and then to the Indian and Pacific Oceans with cooler Antarctic deep and intermediate waters.

Carbon 14 measurements in surface water CO{sub 2} from the Atlantic, India, and Pacific Oceans, 1965--1994

DOE Office of Scientific and Technical Information (OSTI.GOV)

Nydal, R.; Brenkert, A.L.; Boden, T.A.

1998-03-01

In the 1960s, thermonuclear bomb tests released significant pulses of radioactive carbon-14 ({sup 14}C) into the atmosphere. These major perturbations allowed scientists to study the dynamics of the global carbon cycle by calculating rates of isotope exchange between the atmosphere and ocean waters. A total of 950 ocean surface water observations were made from 1965 through 1994. The measurements were taken at 30 stations in the Atlantic Ocean, 14 stations in the Indian Ocean, and 38 stations in the Pacific Ocean. Thirty-two of the 950 samples were taken in the Atlantic Ocean during the R/V Andenes research cruise. {sup 14}Cmore » was measured in 871 of the 950 samples, and those measurements have been corrected ({Delta}{sup 14}C) for isotopic fractionation and radioactive decay. The {Delta}{sup 14}C values range between {minus}113.3 and 280.9 per mille and have a mean value of 101.3 per mille. The highest yearly mean (146.5 per mille) was calculated for 1969, the lowest yearly mean value was calculated for 1990 (67.9 per mille) illustrating a decrease over time. This decrease was to be expected as a result of the ban on atmospheric thermonuclear tests and the slow mixing of the ocean surface waters with the deeper layers.« less

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

The Role of Phytoplankton Dynamics in the Seasonal and Interannual Variability of Carbon in the Subpolar North Atlantic - a Modeling Study

NASA Technical Reports Server (NTRS)

Signorini, Sergio; Hakkinen, Sirpa; Gudmundsson, K.; Olsen, A.; Omar, A. M.; Olafsson, J.; Reverdin, G.; Henson, S. A.; McClain, C. R.; Worthen, D. L.

2014-01-01

We developed an ecosystem/biogeochemical model system, which includes multiple phytoplankton functional groups and carbon cycle dynamics, and applied it to investigate physical-biological interactions in Icelandic waters. Satellite and in situ data were used to evaluate the model. Surface seasonal cycle amplitudes and biases of key parameters (DIC, TA, pCO2, air-sea CO2 flux, and nutrients) are significantly improved when compared to surface observations by prescribing deep water values and trends, based on available data. The seasonality of the coccolithophore and "other phytoplankton" (diatoms and dinoflagellates) blooms is in general agreement with satellite ocean color products. Nutrient supply, biomass and calcite concentrations are modulated by light and mixed layer depth seasonal cycles. Diatoms are the most abundant phytoplankton, with a large bloom in early spring and a secondary bloom in fall. The diatom bloom is followed by blooms of dinoflagellates and coccolithophores. The effect of biological changes on the seasonal variability of the surface ocean pCO2 is nearly twice the temperature effect, in agreement with previous studies. The inclusion of multiple phytoplankton functional groups in the model played a major role in the accurate representation of CO2 uptake by biology. For instance, at the peak of the bloom, the exclusion of coccolithophores causes an increase in alkalinity of up to 4 µmol kg(sup -1) with a corresponding increase in DIC of up to 16 µmol kg(sup -1). During the peak of the bloom in summer, the net effect of the absence of the coccolithophores bloom is an increase in pCO2 of more than 20 µatm and a reduction of atmospheric CO2 uptake of more than 6 mmolm(sup -2) d(sup -1). On average, the impact of coccolithophores is an increase of air-sea CO2 flux of about 27 %. Considering the areal extent of the bloom from satellite images within the Irminger and Icelandic Basins, this reduction translates into an annual mean of nearly 1500 tonnes C yr(sup -1).

Effects of past, present, and future ocean carbon dioxide concentrations on the growth and survival of larval shellfish.

PubMed

Talmage, Stephanie C; Gobler, Christopher J

2010-10-05

The combustion of fossil fuels has enriched levels of CO(2) in the world's oceans and decreased ocean pH. Although the continuation of these processes may alter the growth, survival, and diversity of marine organisms that synthesize CaCO(3) shells, the effects of ocean acidification since the dawn of the industrial revolution are not clear. Here we present experiments that examined the effects of the ocean's past, present, and future (21st and 22nd centuries) CO(2) concentrations on the growth, survival, and condition of larvae of two species of commercially and ecologically valuable bivalve shellfish (Mercenaria mercenaria and Argopecten irradians). Larvae grown under near preindustrial CO(2) concentrations (250 ppm) displayed significantly faster growth and metamorphosis as well as higher survival and lipid accumulation rates compared with individuals reared under modern day CO(2) levels. Bivalves grown under near preindustrial CO(2) levels displayed thicker, more robust shells than individuals grown at present CO(2) concentrations, whereas bivalves exposed to CO(2) levels expected later this century had shells that were malformed and eroded. These results suggest that the ocean acidification that has occurred during the past two centuries may be inhibiting the development and survival of larval shellfish and contributing to global declines of some bivalve populations.

Delayed CO2 emissions from mid-ocean ridge volcanism as a possible cause of late-Pleistocene glacial cycles

NASA Astrophysics Data System (ADS)

Huybers, P. J.

2016-12-01

The coupled variations in ice volume, temperature, and atmospheric CO2 during the late Pleistocene are most often represented as involving some combination of orbital forcing, ice dynamics, and ocean circulation. Also previously argued is that changes in glaciation influence atmospheric CO2 concentrations through modifying subaerial volcanic eruptions and CO2 emissions. Building on recent evidence that ocean ridge volcanism responds to changes in sea level, a conceptual model is presented wherein ocean ridges play an important role in generating late-Pleistocene 100 ky glacial cycles on account of an inherent delay in their feedback response. If all volcanic CO2 emissions responded immediately to changes in pressure, subaerial and ocean-ridge volcanic emissions anomalies would merely oppose one another. At ocean ridges, however, the egress of CO2 from the mantle is delayed by tens-of-thousands of years, or longer, owing to ascent time. The simple model involves temperature, ice, and CO2 and is shown to oscillates at 100 ky time scales when incorporating a delayed CO2 contribution from ocean ridge volcanism, even if the feedback accounts for only a small fraction of total changes in CO2. Features of the model that are consistent with observations include that it readily become phase-locked with insolation forcing associated with changes in Earth's orbit, and that temperature variations lead changes in CO2 by several centuries during deglaciation. Under certain parameterizations, a transition from 41 ky to larger 100 ky oscillations occurs during the middle Pleistocene in response to modulations in orbital forcing. This novel description of Pleistocene glaciation should be testable through ongoing advances in understanding the circulation of carbon through the solid earth.

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

PubMed

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.

Delayed CO2 emissions from mid-ocean ridge volcanism as a possible cause of late-Pleistocene glacial cycles

NASA Astrophysics Data System (ADS)

Huybers, Peter; Langmuir, Charles H.

2017-01-01

The coupled 100,000 year variations in ice volume, temperature, and atmospheric CO2 during the late Pleistocene are generally considered to arise from a combination of orbital forcing, ice dynamics, and ocean circulation. Also previously argued is that changes in glaciation influence atmospheric CO2 concentrations through modifying subaerial volcanic eruptions and CO2 emissions. Building on recent evidence that ocean ridge volcanism responds to changes in sea level, here it is suggested that ocean ridges may play an important role in generating late-Pleistocene 100 ky glacial cycles. If all volcanic CO2 emissions responded immediately to changes in pressure, subaerial and ocean-ridge volcanic emissions anomalies would oppose one another. At ocean ridges, however, the egress of CO2 from the mantle is likely to be delayed by tens-of-thousands of years, or longer, owing to ascent time. A simple model involving temperature, ice, and CO2 is presented that oscillates at ∼100 ky time scales when incorporating a delayed CO2 contribution from ocean ridge volcanism, even if the feedback accounts for only a small fraction of total changes in CO2. Oscillations readily become phase-locked with insolation forcing associated with changes in Earth's orbit. Under certain parameterizations, a transition from ∼40 ky to larger ∼100 ky oscillations occurs during the middle Pleistocene in response to modulations in orbital forcing. This novel description of Pleistocene glaciation should be testable through ongoing advances in understanding the circulation of carbon through the solid earth.

Ocean Winds and Turbulent Air-Sea Fluxes Inferred From Remote Sensing

NASA Technical Reports Server (NTRS)

Bourassa, Mark A.; Gille, Sarah T.; Jackson, Daren L.; Roberts, J. Brent; Wick, Gary A.

2010-01-01

Air-sea turbulent fluxes determine the exchange of momentum, heat, freshwater, and gas between the atmosphere and ocean. These exchange processes are critical to a broad range of research questions spanning length scales from meters to thousands of kilometers and time scales from hours to decades. Examples are discussed (section 2). The estimation of surface turbulent fluxes from satellite is challenging and fraught with considerable errors (section 3); however, recent developments in retrievals (section 3) will greatly reduce these errors. Goals for the future observing system are summarized in section 4. Surface fluxes are defined as the rate per unit area at which something (e.g., momentum, energy, moisture, or CO Z ) is transferred across the air/sea interface. Wind- and buoyancy-driven surface fluxes are called surface turbulent fluxes because the mixing and transport are due to turbulence. Examples of nonturbulent processes are radiative fluxes (e.g., solar radiation) and precipitation (Schmitt et al., 2010). Turbulent fluxes are strongly dependent on wind speed; therefore, observations of wind speed are critical for the calculation of all turbulent surface fluxes. Wind stress, the vertical transport of horizontal momentum, also depends on wind direction. Stress is very important for many ocean processes, including upper ocean currents (Dohan and Maximenko, 2010) and deep ocean currents (Lee et al., 2010). On short time scales, this horizontal transport is usually small compared to surface fluxes. For long-term processes, transport can be very important but again is usually small compared to surface fluxes.

Interactions of the marine phosphorus and carbon cycles

NASA Technical Reports Server (NTRS)

Froelich, P. N.

1984-01-01

About 30 to 50% of the fluvial P-input to the oceans derives from release of reactive-P from particles during their passage through estuaries. The input is matched by P-removal into three approximately equivalent sink: (1) burial in phosphorites on productive shelves; (2) burial with (org) in the deep-sea; and (3) burial with biogenic calcite in the deep-sea. The P/C burial ratio in these three phases is very different: P/C (org) approximately .004; P/C (CaCO3) approximately .001; and P/C (PHOS) approximately .03. The removal mechanisms are all coupled to primary production in the surface ocean, but the details of the feedback mechanisms controlling the steady-state nutrient and carbon budgets in the sea are doscured by lack of knowledge of how the P/C ratios in the sinks adjust, and how shifts in oceanic nutrients affect oceanic ecology and the relative fraction of biogenic CaCO3 and (org) production.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Food web changes under ocean acidification promote herring larvae survival.

PubMed

Sswat, Michael; Stiasny, Martina H; Taucher, Jan; Algueró-Muñiz, Maria; Bach, Lennart T; Jutfelt, Fredrik; Riebesell, Ulf; Clemmesen, Catriona

2018-05-01

Ocean acidification-the decrease in seawater pH due to rising CO 2 concentrations-has been shown to lower survival in early life stages of fish and, as a consequence, the recruitment of populations including commercially important species. To date, ocean-acidification studies with fish larvae have focused on the direct physiological impacts of elevated CO 2 , but largely ignored the potential effects of ocean acidification on food web interactions. In an in situ mesocosm study on Atlantic herring (Clupea harengus) larvae as top predators in a pelagic food web, we account for indirect CO 2 effects on larval survival mediated by changes in food availability. The community was exposed to projected end-of-the-century CO 2 conditions (~760 µatm pCO 2 ) over a period of 113 days. In contrast with laboratory studies that reported a decrease in fish survival, the survival of the herring larvae in situ was significantly enhanced by 19 ± 2%. Analysis of the plankton community dynamics suggested that the herring larvae benefitted from a CO 2 -stimulated increase in primary production. Such indirect effects may counteract the possible direct negative effects of ocean acidification on the survival of fish early life stages. These findings emphasize the need to assess the food web effects of ocean acidification on fish larvae before we can predict even the sign of change in fish recruitment in a high-CO 2 ocean.

A salt oscillator in the glacial Atlantic? 1. The concept

NASA Astrophysics Data System (ADS)

Broecker, Wallace S.; Bond, Gerard; Klas, Millie; Bonani, Georges; Wolfli, Willy

1990-08-01

As shown by the work of Dansgaard and his colleagues, climate oscillations of one or so millennia duration punctuate much of glacial section of the Greenland ice cores. These oscillations are characterized by 5°C air temperature changes, severalfold dust content changes and 50 ppm CO2 changes. Both the temperature and CO2 change are best explained by changes in the mode of operation of the ocean. In this paper we provide evidence which suggests that oscillations in surface water conditions of similar duration are present in the record from a deep sea core at 50°N. Based on this finding, we suggest that the Greenland climate changes are driven by oscillations in the salinity of the Atlantic Ocean which modulate the strength of the Atlantic's conveyor circulation.

Food Supply and Seawater pCO2 Impact Calcification and Internal Shell Dissolution in the Blue Mussel Mytilus edulis

PubMed Central

Melzner, Frank; Stange, Paul; Trübenbach, Katja; Thomsen, Jörn; Casties, Isabel; Panknin, Ulrike; Gorb, Stanislav N.; Gutowska, Magdalena A.

2011-01-01

Progressive ocean acidification due to anthropogenic CO2 emissions will alter marine ecosytem processes. Calcifying organisms might be particularly vulnerable to these alterations in the speciation of the marine carbonate system. While previous research efforts have mainly focused on external dissolution of shells in seawater under saturated with respect to calcium carbonate, the internal shell interface might be more vulnerable to acidification. In the case of the blue mussel Mytilus edulis, high body fluid pCO2 causes low pH and low carbonate concentrations in the extrapallial fluid, which is in direct contact with the inner shell surface. In order to test whether elevated seawater pCO2 impacts calcification and inner shell surface integrity we exposed Baltic M. edulis to four different seawater pCO2 (39, 142, 240, 405 Pa) and two food algae (310–350 cells mL−1 vs. 1600–2000 cells mL−1) concentrations for a period of seven weeks during winter (5°C). We found that low food algae concentrations and high pCO2 values each significantly decreased shell length growth. Internal shell surface corrosion of nacreous ( = aragonite) layers was documented via stereomicroscopy and SEM at the two highest pCO2 treatments in the high food group, while it was found in all treatments in the low food group. Both factors, food and pCO2, significantly influenced the magnitude of inner shell surface dissolution. Our findings illustrate for the first time that integrity of inner shell surfaces is tightly coupled to the animals' energy budget under conditions of CO2 stress. It is likely that under food limited conditions, energy is allocated to more vital processes (e.g. somatic mass maintenance) instead of shell conservation. It is evident from our results that mussels exert significant biological control over the structural integrity of their inner shell surfaces. PMID:21949698

Food supply and seawater pCO2 impact calcification and internal shell dissolution in the blue mussel Mytilus edulis.

PubMed

Melzner, Frank; Stange, Paul; Trübenbach, Katja; Thomsen, Jörn; Casties, Isabel; Panknin, Ulrike; Gorb, Stanislav N; Gutowska, Magdalena A

2011-01-01

Progressive ocean acidification due to anthropogenic CO(2) emissions will alter marine ecosystem processes. Calcifying organisms might be particularly vulnerable to these alterations in the speciation of the marine carbonate system. While previous research efforts have mainly focused on external dissolution of shells in seawater under saturated with respect to calcium carbonate, the internal shell interface might be more vulnerable to acidification. In the case of the blue mussel Mytilus edulis, high body fluid pCO(2) causes low pH and low carbonate concentrations in the extrapallial fluid, which is in direct contact with the inner shell surface. In order to test whether elevated seawater pCO(2) impacts calcification and inner shell surface integrity we exposed Baltic M. edulis to four different seawater pCO(2) (39, 142, 240, 405 Pa) and two food algae (310-350 cells mL(-1) vs. 1600-2000 cells mL(-1)) concentrations for a period of seven weeks during winter (5°C). We found that low food algae concentrations and high pCO(2) values each significantly decreased shell length growth. Internal shell surface corrosion of nacreous ( = aragonite) layers was documented via stereomicroscopy and SEM at the two highest pCO(2) treatments in the high food group, while it was found in all treatments in the low food group. Both factors, food and pCO(2), significantly influenced the magnitude of inner shell surface dissolution. Our findings illustrate for the first time that integrity of inner shell surfaces is tightly coupled to the animals' energy budget under conditions of CO(2) stress. It is likely that under food limited conditions, energy is allocated to more vital processes (e.g. somatic mass maintenance) instead of shell conservation. It is evident from our results that mussels exert significant biological control over the structural integrity of their inner shell surfaces.

Phosphorus, Barium and Bioactive Metals (Zn, Cu, Co) in Coral Aragonite: Relationships to Upper Ocean Productivity

NASA Astrophysics Data System (ADS)

Sherrell, R. M.; Lavigne, M. G.; Linsley, B. K.

2006-12-01

Coral records of surface ocean properties related to primary productivity could reveal much about the history of upper ocean biogeochemistry over decades to centuries, but are currently relatively undeveloped. This presentation will explore the utility of high-resolution records of P/Ca, Ba/Ca, and the micronutrient metals Zn/Ca, Cu/Ca, and Co/Ca. Using high sensitivity laser ablation ICP-MS, we have obtained multi-year records of these variables with ~ bi-weekly resolution and seasonal dating for Porites corals from Rarotonga (21S, 159W) and Clipperton Atoll (10N, 109W) Results are compared to data for Porites and Acropora spp. grown in culture at Rutgers University, to explore the applicability of cultured corals for quantifying the effects of seawater chemistry on trace elements in coralline aragonite. The P/Ca results suggest lattice-bound incorporation and encourage the development of a surface ocean PO4 proxy details will be presented by LaVigne et al. elsewhere in this session. At Rarotonga, Ba/Ca shows regular, ~ annual, 2-5 week duration spikes a factor of 2-3 higher than the ~ constant background signal, appearing in austral spring- summer. These are not associated with runoff or authigenic mineral incorporation, and are similar to Ba spikes observed at least twice in the literature. We explore the hypothesis that these signals are related to biogenic organically-bound or barite Ba in the ambient surface water, and might therefore serve as a proxy of phytoplankton bloom intensity during the most productive part of the year. Potential mechanisms of incorporation must include the possibility of suspended particulate elements finding a route to permanent sequestration in the skeleton. Laser ablation values for Zn, and Cu are similar at Rarotonga and Clipperton, and higher by factors of 500 and 15 than literature values for cleaned aragonite analyzed in solution, while our Co/Ca values are the lowest ever determined. Seasonal and shorter scale variations at Rarotonga are muted for Zn, but substantial for Cu and Co, possibly reflecting biologically-driven changes in ambient dissolved metal concentration or speciation. Corals grown in non-metal clean artificial seawater are higher for Zn, but surprisingly lower for Cu and Co. We suggest that the distribution coefficient model of metal incorporation may need to be revised to include aspects of dissolved metal speciation and particulate metal sources. In sum, these results will be used to evaluate the utility of laser ablation data for revealing aspects of open ocean biogeochemistry in the past.

Alternative OTEC Scheme for a Submarine Robot

NASA Technical Reports Server (NTRS)

Jones, Jack; Chao, Yi

2009-01-01

A proposed system for exploiting the ocean thermal gradient to generate power would be based on the thawing-expansion/ freezing-contraction behavior of a wax or perhaps another suitable phase-change material. The power generated by this system would be used to recharge the batteries in a battery-powered unmanned underwater vehicle [UUV (essentially, a small exploratory submarine robot)] of a type that has been deployed in large numbers in research pertaining to global warming. A UUV of this type travels between the ocean surface and various depths, measuring temperature and salinity. This proposed system would be an alternative to another proposed ocean thermal energy conversion (OTEC) system that would serve the same purpose but would utilize a thermodynamic cycle in which CO2 would be the working fluid. That system is described in Utilizing Ocean Thermal Energy in a Submarine Robot (NPO-43304), immediately following this brief. The main advantage of this proposed system over the one using CO2 is that it could derive a useful amount of energy from a significantly smaller temperature difference. At one phase of its operational cycle, the system now proposed would utilize the surface ocean temperature (which lies between 15 and 20 C over most of the Earth) to melt a wax (e.g., pentadecane) that has a melting/freezing temperature of about 10 C. At the opposite phase of its operational cycle, the system would utilize the lower ocean temperature at depth (e.g., between 4 and 7 C at a depth of 300 m) to freeze the wax. The melting or freezing causes the wax to expand or contract, respectively, by about 8 volume percent.

Numerical modelling of physiological and ecological impacts of ocean acidification on coccolithophores

NASA Astrophysics Data System (ADS)

Furukawa, Makoto; Sato, Toru; Suzuki, Yoshimi; Casareto, Beatriz E.; Hirabayashi, Shinichiro

2018-06-01

Ocean surface acidification due to increasing atmospheric CO2 concentration is currently attracting much attention. Coccolithophores distribute widely across the world's oceans and represent a carbon sink containing about 100 million tonnes of carbon. For this reason, there is concern about dissolution of their shells, which are made of calcium carbonate, due to decreasing pH. In this study, intracellular calcification, photosynthesis, and mass transport through biomembranes of Emiliania huxleyi were modelled numerically for understanding biological response in calcifying organisms. Unknown parameters were optimised by a generic algorithm to match existing experimental results. The model showed that the production of calcium carbonate rather than its dissolution is promoted under an acidified environment. Calcite remains at saturation levels in a coccolith even when it is below saturation levels in the external seawater. Furthermore, a coccolith can dissolve even in water where calcite saturation exceeds 1, because the saturation may be below the threshold level locally around the cell membrane. The present model also showed that the different calcification rates of E. huxleyi with respect to rising CO2 concentrations reported in the literature are due to differences in experimental conditions; in particular, how the CO2 concentration is matched. Lastly, the model was able to reproduce differences in calcification rates among coccolithophore species. The above biochemical-kinetic model was then incorporated into an ecosystem model, and the behaviour of coccolithophores in the ecosystem and the influence of increases in CO2 concentration on water quality were simulated and validated by comparison with existing experimental results. The model also suggests that increased CO2 concentration could lead to an increase in the biomass ratio of coccolithophores to diatoms at high CO2 concentrations, particularly in oligotrophic environments, and to a consequent decrease in pH due to calcium dissolution.

Modelling Biogenic Carbon Cycling and Remineralization In The Mesopelagic Layer 1. Conceptual Development

NASA Astrophysics Data System (ADS)

Legendre, L.; Rivkin, R. B.; Nagata, T.

Most of the biogenic carbon (BC) that is exported (E) from the euphotic zone to the mesopelagic layer (i.e. 100 to 1000 m) is remineralized to CO2 (i.e. respiration, R). A significant part of this remineralized CO2 is ventilated back to the surface layer on decadal time scales, where it equilibrates with the atmosphere. Only the BC that is remineralized or buried (i.e.. sequestration, S) below the permanent pycnocline, typi- cally ca. 1000 m, is isolated from the atmosphere long enough to be of significance to the global climate. Current estimates of E and S for the World Ocean are ca. 7 to 12 and 1 to 2 Gt C/year, respectively. The main biological mechanisms that control R in the mesopelagic layer are the size structure, sinking velocity and chemical composi- tion of E. The interactions among these factors are non-linear. Because the changing climate will modify both R and the downward propagation of characteristics of the surface ocean (e.g. heat, storm mixing), these factors will influence S, which will in turn feedback to climate.

Carbon dioxide supersaturation in the surface waters of lakes

DOE Office of Scientific and Technical Information (OSTI.GOV)

Cole, J.J.; Caraco, N.F.; Kling, G.W.

1994-09-09

Data on the partial pressure of carbon dioxide (CO{sub 2}) in the surface waters from a large number of lakes (1835) with a worldwide distribution show that only a small proportion of the 4665 samples analyzed (less than 10 percent) were within {+-}20 percent of equilibrium with the atmosphere and that most samples (87 percent) were supersaturated. The mean partial pressure of CO{sub 2} averaged 1036 microatmospheres, about three times the value in the overlying atmosphere, indicating that lakes are sources rather than sinks of atmospheric CO{sub 2}. On a global scale, the potential efflux of CO{sub 2} from lakesmore » (about 0.14 x 10{sup 15} grams of carbon per year) is about half as large as riverine transport of organic plus inorganic carbon to the ocean. Lakes are a small but potentially important conduit for carbon for terrestrial sources to the atmospheric sink. 18 refs., 2 figs., 1 tab.« less

Unsteady seasons in the sea

NASA Astrophysics Data System (ADS)

Hauck, Judith

2018-01-01

Ocean uptake of CO2 slows the rate of anthropogenic climate change but comes at the cost of ocean acidification. Observations now show that the seasonal cycle of CO2 in the ocean also changes, leading to earlier occurrence of detrimental conditions for ocean biota.

Biome-specific scaling of ocean productivity, temperature, and carbon export efficiency

NASA Astrophysics Data System (ADS)

Britten, Gregory L.; Primeau, François W.

2016-05-01

Mass conservation and metabolic theory place constraints on how marine export production (EP) scales with net primary productivity (NPP) and sea surface temperature (SST); however, little is empirically known about how these relationships vary across ecologically distinct ocean biomes. Here we compiled in situ observations of EP, NPP, and SST and used statistical model selection theory to demonstrate significant biome-specific scaling relationships among these variables. Multiple statistically similar models yield a threefold variation in the globally integrated carbon flux (~4-12 Pg C yr-1) when applied to climatological satellite-derived NPP and SST. Simulated NPP and SST input variables from a 4×CO2 climate model experiment further show that biome-specific scaling alters the predicted response of EP to simulated increases of atmospheric CO2. These results highlight the need to better understand distinct pathways of carbon export across unique ecological biomes and may help guide proposed efforts for in situ observations of the ocean carbon cycle.

Radiation processing of organics and biological materials exposed to ocean world surface conditions.

NASA Astrophysics Data System (ADS)

Hand, K. P.; Carlson, R. W.

2017-12-01

Assessing the habitability of ocean worlds, such as Europa and Enceladus, motivates a search for endogenous carbon compounds that could be indicative of a habitable, or even inhabited, subsurface liquid water environment. We have examined the role of destruction and synthesis of organic compounds via 10 keV electron bombardment of ices generated under temperature and pressure conditions comparable to Europa and Enceladus. Short-chain organics and ammonia, in combination with water, were exposed to Mrad to Grad doses and observed to evolve to a `lost' carbon fraction (CO and CO2) and a `retained' carbon fraction (consisting of a highly refractory `ocean world tholin' populated by highly radiation resistant carbonyl, aldehyde, and nitrile components). The retained fraction is of key importance as this likely represents the observable fraction for future spacecraft investigations. We also irradiated microbial spores (B. pumilis) to approximately 2 Grad and have found persistence of biomolecule fractions derived from proteins and nucleic acids.

Ocean acidification in a geoengineering context

PubMed Central

Williamson, Phillip; Turley, Carol

2012-01-01

Fundamental changes to marine chemistry are occurring because of increasing carbon dioxide (CO2) in the atmosphere. Ocean acidity (H+ concentration) and bicarbonate ion concentrations are increasing, whereas carbonate ion concentrations are decreasing. There has already been an average pH decrease of 0.1 in the upper ocean, and continued unconstrained carbon emissions would further reduce average upper ocean pH by approximately 0.3 by 2100. Laboratory experiments, observations and projections indicate that such ocean acidification may have ecological and biogeochemical impacts that last for many thousands of years. The future magnitude of such effects will be very closely linked to atmospheric CO2; they will, therefore, depend on the success of emission reduction, and could also be constrained by geoengineering based on most carbon dioxide removal (CDR) techniques. However, some ocean-based CDR approaches would (if deployed on a climatically significant scale) re-locate acidification from the upper ocean to the seafloor or elsewhere in the ocean interior. If solar radiation management were to be the main policy response to counteract global warming, ocean acidification would continue to be driven by increases in atmospheric CO2, although with additional temperature-related effects on CO2 and CaCO3 solubility and terrestrial carbon sequestration. PMID:22869801

Deglacial climate, carbon cycle and ocean chemistry changes in response to a terrestrial carbon release

NASA Astrophysics Data System (ADS)

Simmons, C. T.; Matthews, H. D.; Mysak, L. A.

2016-02-01

Researchers have proposed that a significant portion of the post-glacial rise in atmospheric CO2 could be due to the respiration of permafrost carbon stocks that formed over the course of glaciation. In this paper, we used the University of Victoria Earth System Climate Model v. 2.9 to simulate the deglacial and interglacial carbon cycle from the last glacial maximum to the present. The model's sensitivity to mid and high latitude terrestrial carbon storage is evaluated by including a 600 Pg C carbon pool parameterized to respire in concert with decreases in ice sheet surface area. The respiration of this stored carbon during the early stages of deglaciation had a large effect on the carbon cycle in these simulations, allowing atmospheric CO2 to increase by 40 ppmv in the model, with an additional 20 ppmv increase occurring in the case of a more realistic, prescribed CO2 radiative warming. These increases occurred prior to large-scale carbon uptake due to the reestablishment of boreal forests and peatlands in the proxy record (beginning in the early Holocene). Surprisingly, the large external carbon input to the atmosphere and oceans did not increase sediment dissolution and mean ocean alkalinity relative to a control simulation without the high latitude carbon reservoir. In addition, our simulations suggest that an early deglacial terrestrial carbon release may come closer to explaining some observed deglacial changes in deep-ocean carbonate concentrations than simulations without such a release. We conclude that the respiration of glacial soil carbon stores may have been an important contributor to the deglacial CO2 rise, particularly in the early stages of deglaciation.

The persistent and pernicious myth of the early CO2-N2 atmospheres of terrestrial planets

NASA Astrophysics Data System (ADS)

Shaw, G. H.

2009-12-01

The accepted model for early atmospheres of terrestrial planets has settled on a CO2-N2 composition. Unfortunately, while it is largely based on a brilliant geological analysis by Rubey, there is no compelling evidence whatsoever for such a composition as the first “permanent” atmosphere for Earth or any other planet. In fact, geological discoveries of the past 50+ years reveal several problems with a CO2-N2 atmosphere, some of which Rubey recognized in his own analysis. He clearly addressed the problem of timing of degassing, concluding that early massive degassing of CO2 would produce readily observed and profound effects, which are not evident. Modeling and constraints on the timing of planetary accretion and core formation indicate massive early degassing. If early degassing emitted CO2-N2, the effects are concealed. Plate tectonic recycling is not a solution, as conditions would have persisted beyond the time of the earliest rocks, which do not show the effects. Attempts to return degassed CO2 to the mantle are not only ad hoc, but inconsistent with early thermal structure of the Earth. Second, production of prebiotic organic compounds from a CO2-N2 atmosphere has been a nagging problem. At best this has been addressed by invoking hydrogen production from the mantle to provide reducing capacity. While hydrogen may be emitted in volcanic eruptions, it is exceedingly difficult to imagine this process generating enough organics to yield high concentrations in a global ocean. The recent fashion of invoking organic synthesis at deep-sea vents suffers from the same problem: how to achieve sufficient concentrations of organics in a global ocean by abiotic synthesis when hydrothermal activity stirs the solution and carries the prebiotic products off to great dilution? Suggesting life began at deep-sea vents, and continues to carry on chemosynthesis there, begs the question. Unless you get high enough concentrations of prebiotics by abiotic processes, you simply don’t get life. Third, solutions invoking high atmospheric CO2 as the answer to the faint young sun problem encounter exactly the same problems associated with prompt degassing of CO2. Fourth, the carbon isotope record, in which early carbonaceous deposits show signs of photosynthetic fractionation of carbon are problematical if most of the primary surface and near-surface carbon was CO2. Finally, the delay in oxidation of Earth’s surface following oxygenic photosynthesis is problematical if early photosynthesizers had a vast CO2 source from early degassing. Given an abundant food supply, what prevented early cyanobacteria from rapidly oxidizing the surface? Although discovery of CO2-rich atmospheres on Venus and Mars seem to support CO2 as the primary surface carbon reservoir, these atmospheres are the result of atmospheric evolution, particularly loss of H to space. ALL of these problems disappear with early degassing of reduced gases such as CH4 and NH3. Considerations of meteoritic compositions, accretionary processes, and early atmosphere/hydrosphere chemical processing all support reduced gases as dominant in the early atmospheres of the terrestrial planets. The time has come to revert to any earlier idea of strongly reducing conditions on early terrestrial planet surfaces, followed by long-term evolutionary trends toward oxidation.

Ocean acidification: the other CO2 problem.

PubMed

Doney, Scott C; Fabry, Victoria J; Feely, Richard A; Kleypas, Joan A

2009-01-01

Rising atmospheric carbon dioxide (CO2), primarily from human fossil fuel combustion, reduces ocean pH and causes wholesale shifts in seawater carbonate chemistry. The process of ocean acidification is well documented in field data, and the rate will accelerate over this century unless future CO2 emissions are curbed dramatically. Acidification alters seawater chemical speciation and biogeochemical cycles of many elements and compounds. One well-known effect is the lowering of calcium carbonate saturation states, which impacts shell-forming marine organisms from plankton to benthic molluscs, echinoderms, and corals. Many calcifying species exhibit reduced calcification and growth rates in laboratory experiments under high-CO2 conditions. Ocean acidification also causes an increase in carbon fixation rates in some photosynthetic organisms (both calcifying and noncalcifying). The potential for marine organisms to adapt to increasing CO2 and broader implications for ocean ecosystems are not well known; both are high priorities for future research. Although ocean pH has varied in the geological past, paleo-events may be only imperfect analogs to current conditions.

Enhancement of non-CO2 radiative forcing via intensified carbon cycle feedbacks

NASA Astrophysics Data System (ADS)

MacDougall, Andrew H.; Knutti, Reto

2016-06-01

The global carbon cycle is sensitive to changes in global temperature and atmospheric CO2 concentration, with increased temperature tending to reduce the efficiency of carbon sinks and increased CO2 enhancing the efficiency of carbon sinks. The emission of non-CO2 greenhouse gases warms the Earth but does not induce the CO2 fertilization effect or increase the partial-pressure gradient between the atmosphere and the surface ocean. Here we present idealized climate model experiments that explore the indirect interaction between non-CO2 forcing and the carbon cycle. The experiments suggest that this interaction enhances the warming effect of the non-CO2 forcing by up to 25% after 150 years and that much of the warming caused by these agents lingers for over 100 years after the dissipation of the non-CO2 forcing. Overall, our results suggest that the longer emissions of non-CO2 forcing agents persists the greater effect these agents will have on global climate.

Effects of eustatic sea-level change, ocean dynamics, and nutrient utilization on atmospheric pCO2 and seawater composition over the last 130 000 years: a model study

NASA Astrophysics Data System (ADS)

Wallmann, K.; Schneider, B.; Sarnthein, M.

2016-02-01

We have developed and employed an Earth system model to explore the forcings of atmospheric pCO2 change and the chemical and isotopic evolution of seawater over the last glacial cycle. Concentrations of dissolved phosphorus (DP), reactive nitrogen, molecular oxygen, dissolved inorganic carbon (DIC), total alkalinity (TA), 13C-DIC, and 14C-DIC were calculated for 24 ocean boxes. The bi-directional water fluxes between these model boxes were derived from a 3-D circulation field of the modern ocean (Opa 8.2, NEMO) and tuned such that tracer distributions calculated by the box model were consistent with observational data from the modern ocean. To model the last 130 kyr, we employed records of past changes in sea-level, ocean circulation, and dust deposition. According to the model, about half of the glacial pCO2 drawdown may be attributed to marine regressions. The glacial sea-level low-stands implied steepened ocean margins, a reduced burial of particulate organic carbon, phosphorus, and neritic carbonate at the margin seafloor, a decline in benthic denitrification, and enhanced weathering of emerged shelf sediments. In turn, low-stands led to a distinct rise in the standing stocks of DIC, TA, and nutrients in the global ocean, promoted the glacial sequestration of atmospheric CO2 in the ocean, and added 13C- and 14C-depleted DIC to the ocean as recorded in benthic foraminifera signals. The other half of the glacial drop in pCO2 was linked to inferred shoaling of Atlantic meridional overturning circulation and more efficient utilization of nutrients in the Southern Ocean. The diminished ventilation of deep water in the glacial Atlantic and Southern Ocean led to significant 14C depletions with respect to the atmosphere. According to our model, the deglacial rapid and stepwise rise in atmospheric pCO2 was induced by upwelling both in the Southern Ocean and subarctic North Pacific and promoted by a drop in nutrient utilization in the Southern Ocean. The deglacial sea-level rise led to a gradual decline in nutrient, DIC, and TA stocks, a slow change due to the large size and extended residence times of dissolved chemical species in the ocean. Thus, the rapid deglacial rise in pCO2 can be explained by fast changes in ocean dynamics and nutrient utilization whereas the gradual pCO2 rise over the Holocene may be linked to the slow drop in nutrient and TA stocks that continued to promote an ongoing CO2 transfer from the ocean into the atmosphere.

Decadal trends in regional CO2 fluxes estimated from atmospheric inversions

NASA Astrophysics Data System (ADS)

Saeki, T.; Patra, P. K.

2016-12-01

Top-down approach (or atmospheric inversion) using atmospheric transport models and CO2 observations are an effective way to optimize surface fluxes at subcontinental scales and monthly time intervals. We used the CCSR/NIES/FRCGC AGCM-based Chemistry Transport Model (JAMSTEC's ACTM) and atmospheric CO2 concentrations at NOAA, CSIRO, JMA, NIES, NIES-MRI sites from Obspack GLOBALVIEW-CO2 data product (2013) for estimating CO2 fluxes for the period of 1990-2011. Carbon fluxes were estimated for 84 partitions (54 lands + 30 oceans) of the globe by using a Bayesian synthesis inversion framework. A priori fluxes are (1) atmosphere-ocean exchange from Takahashi et al. (2009), (2) 3-hourly terrestrial biosphere fluxes (annually balanced) from CASA model, and (3) fossil fuel fluxes from CDIAC global totals and EDGAR4.2 spatial distributions. Four inversion cases have been tested with 1) 21 sites (sites which have real data fraction of 90 % or more for 1989-2012), 2) 21 sites + CONTRAIL data, 3) 66 sites (over 70 % coverage), and 4) 157 sites. As a result of time-dependent inversions, mean total flux (excluding fossil fuel) for the period 1990-2011 is estimated to be -3.09 ±0.16 PgC/yr (mean and standard deviation of the four cases), where land (incl. biomass burning and land use change) and ocean absorb an average rate of -1.80 ±0.18 and -1.29 ±0.08 PgC/yr, respectively. The average global total sink from 1991-2000 to 2001-2010 increases by about 0.5 PgC/yr, mainly due to the increase in northern and tropical land sinks (Africa, Boreal Eurasia, East Asia and Europe), while ocean sinks show no clear trend. Inversion with CONTRAIL data estimates large positive flux anomalies in late 1997 associated with the 1997/98 El-Nino, while inversion without CONTARIL data between Japan and Australia fails to estimate such large anomalies. Acknowledgements. This work is supported by the Environment Research and Technology Development Fund (2-1401) of the Ministry of the Environment, Japan. We thank all measurement groups for submitting CO2 concentration data to the obspack-GLOBALVIEW product.

Effects of sea-ice and biogeochemical processes and storms on under-ice water fCO2 during the winter-spring transition in the high Arctic Ocean: Implications for sea-air CO2 fluxes

NASA Astrophysics Data System (ADS)

Fransson, Agneta; Chierici, Melissa; Skjelvan, Ingunn; Olsen, Are; Assmy, Philipp; Peterson, Algot K.; Spreen, Gunnar; Ward, Brian

2017-07-01

We performed measurements of carbon dioxide fugacity (fCO2) in the surface water under Arctic sea ice from January to June 2015 during the Norwegian young sea ICE (N-ICE2015) expedition. Over this period, the ship drifted with four different ice floes and covered the deep Nansen Basin, the slopes north of Svalbard, and the Yermak Plateau. This unique winter-to-spring data set includes the first winter-time under-ice water fCO2 observations in this region. The observed under-ice fCO2 ranged between 315 µatm in winter and 153 µatm in spring, hence was undersaturated relative to the atmospheric fCO2. Although the sea ice partly prevented direct CO2 exchange between ocean and atmosphere, frequently occurring leads and breakup of the ice sheet promoted sea-air CO2 fluxes. The CO2 sink varied between 0.3 and 86 mmol C m-2 d-1, depending strongly on the open-water fractions (OW) and storm events. The maximum sea-air CO2 fluxes occurred during storm events in February and June. In winter, the main drivers of the change in under-ice water fCO2 were dissolution of CaCO3 (ikaite) and vertical mixing. In June, in addition to these processes, primary production and sea-air CO2 fluxes were important. The cumulative loss due to CaCO3 dissolution of 0.7 mol C m-2 in the upper 10 m played a major role in sustaining the undersaturation of fCO2 during the entire study. The relative effects of the total fCO2 change due to CaCO3 dissolution was 38%, primary production 26%, vertical mixing 16%, sea-air CO2 fluxes 16%, and temperature and salinity insignificant.

DOE Office of Scientific and Technical Information (OSTI.GOV)

MacDonald, G.; Abarbanel, H.; Carruthers, P.

If the current growth rate in the use of fossil fuels continues at 4.3% per year, then the CO/sub 2/ concentration in the atmosphere can be expected to double by about 2035 provided the current partition of CO/sub 2/ between the atmosphere, biosphere, and oceans is maintained as is the current mix of fuels. Slower rates of anticipated growth of energy use lead to a doubling of the carbon content of the atmosphere sometime in the period 2040 to 2060. This report addresses the questions of the sources of atmospheric CO/sub 2/; considers distribution of the present CO/sub 2/ amongmore » the atmospheric, oceanic, and biospheric reservoir; and assesses the impact on climate as reflected by the average ground temperature at each latitude of significant increases in atmospheric CO/sub 2/. An analytic model of the atmosphere was constructed (JASON Climate Model). Calculation with this zonally averaged model shows an increase of average surface temperature of 2.4/sup 0/ for a doubling of CO/sub 2/. The equatorial temperature increases by 0.7/sup 0/K, while the poles warm up by 10 to 12/sup 0/K. The warming of climate will not necessarily lead to improved living conditions everywhere. Changes in sea level, in agricultural productivity, and in water availability can be anticipated, but the dimensions of their economic, political, or social consequences can not.« less

Baseline Monitoring of the Western Arctic Ocean Estimates 20% of Canadian Basin Surface Waters Are Undersaturated with Respect to Aragonite

PubMed Central

Robbins, Lisa L.; Wynn, Jonathan G.; Lisle, John T.; Yates, Kimberly K.; Knorr, Paul O.; Byrne, Robert H.; Liu, Xuewu; Patsavas, Mark C.; Azetsu-Scott, Kumiko; Takahashi, Taro

2013-01-01

Marine surface waters are being acidified due to uptake of anthropogenic carbon dioxide, resulting in surface ocean areas of undersaturation with respect to carbonate minerals, including aragonite. In the Arctic Ocean, acidification is expected to occur at an accelerated rate with respect to the global oceans, but a paucity of baseline data has limited our understanding of the extent of Arctic undersaturation and of regional variations in rates and causes. The lack of data has also hindered refinement of models aimed at projecting future trends of ocean acidification. Here, based on more than 34,000 data records collected in 2010 and 2011, we establish a baseline of inorganic carbon data (pH, total alkalinity, dissolved inorganic carbon, partial pressure of carbon dioxide, and aragonite saturation index) for the western Arctic Ocean. This data set documents aragonite undersaturation in ∼20% of the surface waters of the combined Canada and Makarov basins, an area characterized by recent acceleration of sea ice loss. Conservative tracer studies using stable oxygen isotopic data from 307 sites show that while the entire surface of this area receives abundant freshwater from meteoric sources, freshwater from sea ice melt is most closely linked to the areas of carbonate mineral undersaturation. These data link the Arctic Ocean’s largest area of aragonite undersaturation to sea ice melt and atmospheric CO2 absorption in areas of low buffering capacity. Some relatively supersaturated areas can be linked to localized biological activity. Collectively, these observations can be used to project trends of ocean acidification in higher latitude marine surface waters where inorganic carbon chemistry is largely influenced by sea ice meltwater. PMID:24040074

Baseline monitoring of the western Arctic Ocean estimates 20% of the Canadian Basin surface waters are undersaturated with respect to aragonite

USGS Publications Warehouse

Robbins, Lisa L.; Wynn, Jonathan G.; Lisle, John T.; Yates, Kimberly K.; Knorr, Paul O.; Byrne, Robert H.; Liu, Xuewu; Patsavas, Mark C.; Azetsu-Scott, Kumiko; Takahashi, Taro

2013-01-01

Marine surface waters are being acidified due to uptake of anthropogenic carbon dioxide, resulting in surface ocean areas of undersaturation with respect to carbonate minerals, including aragonite. In the Arctic Ocean, acidification is expected to occur at an accelerated rate with respect to the global oceans, but a paucity of baseline data has limited our understanding of the extent of Arctic undersaturation and of regional variations in rates and causes. The lack of data has also hindered refinement of models aimed at projecting future trends of ocean acidification. Here, based on more than 34,000 data records collected in 2010 and 2011, we establish a baseline of inorganic carbon data (pH, total alkalinity, dissolved inorganic carbon, partial pressure of carbon dioxide, and aragonite saturation index) for the western Arctic Ocean. This data set documents aragonite undersaturation in ~20% of the surface waters of the combined Canada and Makarov basins, an area characterized by recent acceleration of sea ice loss. Conservative tracer studies using stable oxygen isotopic data from 307 sites show that while the entire surface of this area receives abundant freshwater from meteoric sources, freshwater from sea ice melt is most closely linked to the areas of carbonate mineral undersaturation. These data link the Arctic Ocean’s largest area of aragonite undersaturation to sea ice melt and atmospheric CO2 absorption in areas of low buffering capacity. Some relatively supersaturated areas can be linked to localized biological activity. Collectively, these observations can be used to project trends of ocean acidification in higher latitude marine surface waters where inorganic carbon chemistry is largely influenced by sea ice meltwater.

Antarctic Ocean Nutrient Conditions During the Last Two Glacial Cycles

NASA Astrophysics Data System (ADS)

Studer, A.; Sigman, D. M.; Martinez-Garcia, A.; Benz, V.; Winckler, G.; Kuhn, G.; Esper, O.; Lamy, F.; Jaccard, S.; Wacker, L.; Oleynik, S.; Gersonde, R.; Haug, G. H.

2014-12-01

The high concentration of the major nutrients nitrate and phosphate in the Antarctic Zone of the Southern Ocean dictates the nature of Southern Ocean ecosystems and permits these nutrients to be carried from the deep ocean into the nutrient-limited low latitudes. Incomplete nutrient consumption in the Antarctic also allows the leakage of deeply sequestered carbon dioxide (CO2) back to the atmosphere, and changes in this leakage may have driven glacial/interglacial cycles in atmospheric CO2. In a sediment core from the Pacific sector of the Antarctic Ocean, we report diatom-bound N isotope (δ15Ndb) records for total recoverable diatoms and two assemblages of diatom species. These data indicate tight coupling between the degree of nitrate consumption and Antarctic climate across the last two glacial cycles, with δ15Ndb (and thus the degree of nitrate consumption) increasing at each major Antarctic cooling event. Measurements in the same sediment core indicate that export production was reduced during ice ages, pointing to an ice age reduction in the supply of deep ocean-sourced nitrate to the Antarctic Ocean surface. The reduced export production of peak ice ages also implies a weaker winter-to-summer decline (i.e. reduced seasonality) in mixed layer nitrate concentration, providing a plausible explanation for an observed reduction in the inter-assemblage δ15Ndb difference during these coldest times. Despite the weak summertime productivity, the reduction in wintertime nitrate supply from deep waters left the Antarctic mixed layer with a low nitrate concentration, and this wintertime change also would have reduced the outgassing of CO2. Relief of light limitation fails to explain the intermediate degree of nitrate consumption that characterizes early glacial conditions, as improved light limitation coincident with reduced nitrate supply would drive nitrate consumption to completion. Thus, the data favor iron availability as the dominant control on annual Antarctic Ocean export production over glacial cycles.

Ocean Ridges and Oxygen

NASA Astrophysics Data System (ADS)

Langmuir, C. H.

2014-12-01

The history of oxygen and the fluxes and feedbacks that lead to its evolution through time remain poorly constrained. It is not clear whether oxygen has had discrete steady state levels at different times in Earth's history, or whether oxygen evolution is more progressive, with trigger points that lead to discrete changes in markers such as mass independent sulfur isotopes. Whatever this history may have been, ocean ridges play an important and poorly recognized part in the overall mass balance of oxidants and reductants that contribute to electron mass balance and the oxygen budget. One example is the current steady state O2 in the atmosphere. The carbon isotope data suggest that the fraction of carbon has increased in the Phanerozoic, and CO2 outgassing followed by organic matter burial should continually supply more O2 to the surface reservoirs. Why is O2 not then increasing? A traditional answer to this question would relate to variations in the fraction of burial of organic matter, but this fraction appears to have been relatively high throughout the Phanerozoic. Furthermore, subduction of carbon in the 1/5 organic/carbonate proportions would contribute further to an increasingly oxidized surface. What is needed is a flux of oxidized material out of the system. One solution would be a modern oxidized flux to the mantle. The current outgassing flux of CO2 is ~3.4*1012 moles per year. If 20% of that becomes stored organic carbon, that is a flux of .68*1012 moles per year of reduced carbon. The current flux of oxidized iron in subducting ocean crust is ~2*1012 moles per year of O2 equivalents, based on the Fe3+/Fe2+ ratios in old ocean crust compared to fresh basalts at the ridge axis. This flux more than accounts for the incremental oxidizing power produced by modern life. It also suggests a possible feedback through oxygenation of the ocean. A reduced deep ocean would inhibit oxidation of ocean crust, in which case there would be no subduction flux of oxidized material, and oxygen could rise. Once the ocean becomes fully oxidized, a substantial subduction flux operates as a negative feedback. Plate tectonic geochemical cycles may have played a very significant role in the oxygen balance in both the ancient and modern Earth.

Revisiting ocean carbon sequestration by direct injection: A global carbon budget perspective Fabian Reith, David P. Keller & Andreas Oschlies

NASA Astrophysics Data System (ADS)

Reith, F.; Keller, D. P.; Martin, T.; Oschlies, A.

2015-12-01

Marchetti [1977] proposed that CO2 could be directly injected into the deep ocean to mitigate its rapid build-up in the atmosphere. Although previous studies have investigated biogeochemical and climatic effects of injecting CO2 into the ocean, they have not looked at global carbon cycle feedbacks and backfluxes that are important for accounting. Using an Earth System Model of intermediate complexity we simulated the injection of CO2 into the deep ocean during a high CO2 emissions scenario. At seven sites 0.1 GtC yr-1 was injected at three different depths (3 separate experiments) between the years 2020 and 2120. After the 100-year injection period, our simulations continued until the year 3020 to assess the long-term dynamics. In addition, we investigated the effects of marine sediment feedbacks during the experiments by running the model with and without a sediment sub-model. Our results, in regards to efficiency (the residence time of injected CO2) and seawater chemistry changes, are similar to previous studies. However, from a carbon budget perspective the targeted cumulative atmospheric CO2 reduction of 70 GtC was never reached. This was caused by the atmosphere-to-terrestrial and/or atmosphere-to-ocean carbon fluxes (relative to the control run), which were effected by the reduction in atmospheric carbon. With respect to global oceanic carbon, the respective carbon cycle-climate feedbacks led to an even smaller efficiency than indicated by tracing the injected CO2. The ocean also unexpectedly took up carbon after the injection at 1500 m was stopped because of a deep convection event in the Southern Ocean. These findings highlighted that the accounting of CO2 injection would be challenging.

Use of a Land-Based, Dual-Parameter Analyzer for Tracking Ocean Acidification in Nearshore Coastal Habitats

NASA Astrophysics Data System (ADS)

Shea, M.; Alin, S. R.; Evans, W.; Sutton, A.; Hales, B. R.; Newton, J.; Feely, R. A.

2016-12-01

In 2007 to 2008, U.S. Pacific Northwest shellfish hatcheries experienced unprecedented larval mortality, attributed to upwelling along the Washington-Oregon coast that brought seawater enriched in anthropogenic CO2 and undersaturated with respect to aragonite to the surface. In response, several hatcheries have been outfitted with land-based analyzers to measure CO2 partial pressure (pCO2) and total dissolved CO2 (TCO2) through U.S. IOOS and NOAA OAP funding. This analyzer, developed at Oregon State University and known as the `Burke-O-Lator,' allows users to track CO2 system parameters in real-time. The data are available in near real-time on the IOOS Pacific Region Ocean Acidification (IPACOA) data portal, which feeds to the Global Ocean Acidification Observing Network (GOA-ON). Here, we explore the broader use of this system as an environmental monitoring tool. Most of the high-quality OA time-series locations in GOA-ON are in the open and coastal ocean, yet many areas of biological interest—such as shellfish hatcheries, shellfish farms, and coastal laboratories—are in the nearshore area of the coastal zone. A truly globally integrated assessment of OA must include nearshore conditions, which have been shown to be quite different in terms of variability, drivers, and range. We evaluated two pCO2 time-series from the coastal nearshore: the Taylor Shellfish Hatchery Burke-O-Lator system on the shore of Dabob Bay in Puget Sound, WA, and the nearby but offshore Dabob ORCA buoy MAPCO2 system within the bay. Preliminary comparison of three years of data reveals similar patterns despite differences in location and seawater intake depth, highlighting the opportunity for the addition of coupled nearshore biology and biogeochemistry measurements in GOA-ON. In addition, the well-calibrated, dual-parameter nature of the system is important for constraining nearshore chemistry, as biology, groundwater, and river inputs can lead to strong variability in carbonate chemistry and the potential for decoupled pH and aragonite saturation state dynamics. With the increasing threat of corrosive conditions due to ocean acidification, continued work on integrating the now seven Burke-O-Lator sites into GOA-ON will improve our ability to understand, monitor, mitigate, and adapt to nearshore carbonate chemistry.

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

NASA Astrophysics Data System (ADS)

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 more affected by bubble injection, and reacts differently to temperature change. Oxygen is also produced and consumed by photosynthesis and respiration respectively at a specific ratio to CO2. These properties enable us to use oxygen as a separate constraint from carbon to determine the effect these various processes have on gas cycling, and the global ocean circulation.

Ocean alkalinity and the Cretaceous/Tertiary boundary

NASA Technical Reports Server (NTRS)

Caldeira, K. G.; Rampino, Michael R.

1988-01-01

A biogeochemical cycle model resolving ocean carbon and alkalinity content is applied to the Maestrichtian and Danian. The model computes oceanic concentrations and distributions of Ca(2+), Mg(2+), and Sigma-CO2. From these values an atmospheric pCO2 value is calculated, which is used to estimate rates of terrestrial weathering of calcite, dolomite, and calcium and magnesium silicates. Metamorphism of carbonate rocks and the subsequent outgassing of CO2 to the atmosphere are parameterized in terms of carbonate rock reservoir sizes, total land area, and a measure of overall tectonic activity, the sea-floor generation rate. The ocean carbon reservoir computed by the model is used with Deep Sea Drilling Project (DSDP) C-13 data to estimate organic detrital fluxes under a variety of ocean mixing rate assumptions. Using Redfield ratios, the biogenic detrital flux estimate is used to partition the ocean carbon and alkalinity reservoirs between the mixed layer and deep ocean. The calcite flux estimate and carbonate ion concentrations are used to determine the rate of biologically mediated CaCO3 titration. Oceanic productivity was severely limited for approximately 500 kyr following the K/T boundary resulting in significant increases in total ocean alkalinity. As productivity returned to the ocean, excess carbon and alkalinity was removed from the ocean as CaCO3. Model runs indicate that this resulted in a transient imbalance in the other direction. Ocean chemistry returned to near-equilibrium by about 64 mybp.

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

PubMed

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

2017-01-01

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

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

PubMed Central

Fabricius, Katharina E.; Munday, Philip L.

2017-01-01

Quantifying the amount of carbon dioxide (CO2) in seawater is an essential component of ocean acidification research; however, equipment for measuring CO2 directly can be costly and involve complex, bulky apparatus. Consequently, other parameters of the carbonate system, such as pH and total alkalinity (AT), are often measured and used to calculate the partial pressure of CO2 (pCO2) in seawater, especially in biological CO2-manipulation studies, including large ecological experiments and those conducted at field sites. Here we compare four methods of pCO2 determination that have been used in biological ocean acidification experiments: 1) Versatile INstrument for the Determination of Total inorganic carbon and titration Alkalinity (VINDTA) measurement of dissolved inorganic carbon (CT) and AT, 2) spectrophotometric measurement of pHT and AT, 3) electrode measurement of pHNBS and AT, and 4) the direct measurement of CO2 using a portable CO2 equilibrator with a non-dispersive infrared (NDIR) gas analyser. In this study, we found these four methods can produce very similar pCO2 estimates, and the three methods often suited to field-based application (spectrophotometric pHT, electrode pHNBS and CO2 equilibrator) produced estimated measurement uncertainties of 3.5–4.6% for pCO2. Importantly, we are not advocating the replacement of established methods to measure seawater carbonate chemistry, particularly for high-accuracy quantification of carbonate parameters in seawater such as open ocean chemistry, for real-time measures of ocean change, nor for the measurement of small changes in seawater pCO2. However, for biological CO2-manipulation experiments measuring differences of over 100 μatm pCO2 among treatments, we find the four methods described here can produce similar results with careful use. PMID:28957378

Coccolithophore growth and calcification in a changing ocean

NASA Astrophysics Data System (ADS)

Krumhardt, Kristen M.; Lovenduski, Nicole S.; Iglesias-Rodriguez, M. Debora; Kleypas, Joan A.

2017-12-01

Coccolithophores are the most abundant calcifying phytoplankton in the ocean. These tiny primary producers have an important role in the global carbon cycle, substantially contributing to global ocean calcification, ballasting organic matter to the deep sea, forming part of the marine food web base, and influencing ocean-atmosphere CO2 exchange. Despite these important impacts, coccolithophores are not explicitly simulated in most marine ecosystem models and, therefore, their impacts on carbon cycling are not represented in most Earth system models. Here, we compile field and laboratory data to synthesize overarching, across-species relationships between environmental conditions and coccolithophore growth rates and relative calcification (reported as a ratio of particulate inorganic carbon to particulate organic carbon in coccolithophore biomass, PIC/POC). We apply our relationships in a generalized coccolithophore model, estimating current surface ocean coccolithophore growth rates and relative calcification, and projecting how these may change over the 21st century using output from the Community Earth System Model large ensemble. We find that average increases in sea surface temperature of ∼ 2-3 ° C lead to faster coccolithophore growth rates globally (> 10% increase) and increased calcification at high latitudes. Roughly an ubiquitous doubling of surface ocean pCO2 by the end of the century has the potential to moderately stimulate coccolithophore growth rates, but leads to reduced calcification (∼ 25% decrease). Decreasing nutrient availability (from warming-induced increases in stratification) produces increases in relative calcification, but leads to ∼ 25% slower growth rates. With all drivers combined, we observe decreases in calcification and growth in most low and mid latitude regions, with possible increases in both of these responses in most high latitude regions. Major limitations of our coccolithophore model stem from a lack of conclusive physiological responses to changes in irradiance (we do not include light limitation in our model), and a lack of physiological data for major coccolithophore species. Species within the Umbellosphaera genus, for example, are dominant in mid to low latitude regions where we predict some of the largest decreases in coccolithophore growth rate and calcification.

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

NASA Astrophysics Data System (ADS)

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

2018-05-01

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

Ice Melt, Sea Level Rise and Superstorms: Evidence from Paleoclimate Data, Climate Modeling, and Modern Observations that 2C Global Warming Could Be Dangerous

NASA Technical Reports Server (NTRS)

Hansen, J.; Sato, Makiko; Hearty, Paul; Ruedy, Reto; Kelley, Maxwell; Masson-Delmotte, Valerie; Russell, Gary; Tselioudis, George; Cao, Junji; Rignot, Eric;

Ice melt, sea level rise and superstorms: evidence from paleoclimate data, climate modeling, and modern observations that 2 °C global warming could be dangerous

NASA Astrophysics Data System (ADS)

Hansen, James; Sato, Makiko; Hearty, Paul; Ruedy, Reto; Kelley, Maxwell; Masson-Delmotte, Valerie; Russell, Gary; Tselioudis, George; Cao, Junji; Rignot, Eric; Velicogna, Isabella; Tormey, Blair; Donovan, Bailey; Kandiano, Evgeniya; von Schuckmann, Karina; Kharecha, Pushker; Legrande, Allegra N.; Bauer, Michael; Lo, Kwok-Wai

2016-03-01

We use numerical climate simulations, paleoclimate data, and modern observations to study the effect of growing ice melt from Antarctica and Greenland. Meltwater tends to stabilize the ocean column, inducing amplifying feedbacks that increase subsurface ocean warming and ice shelf melting. Cold meltwater and induced dynamical effects cause ocean surface cooling in the Southern Ocean and North Atlantic, thus increasing Earth's energy imbalance and heat flux into most of the global ocean's surface. Southern Ocean surface cooling, while lower latitudes are warming, increases precipitation on the Southern Ocean, increasing ocean stratification, slowing deepwater formation, and increasing ice sheet mass loss. These feedbacks make ice sheets in contact with the ocean vulnerable to accelerating disintegration. We hypothesize that ice mass loss from the most vulnerable ice, sufficient to raise sea level several meters, is better approximated as exponential than by a more linear response. Doubling times of 10, 20 or 40 years yield multi-meter sea level rise in about 50, 100 or 200 years. Recent ice melt doubling times are near the lower end of the 10-40-year range, but the record is too short to confirm the nature of the response. The feedbacks, including subsurface ocean warming, help explain paleoclimate data and point to a dominant Southern Ocean role in controlling atmospheric CO2, which in turn exercised tight control on global temperature and sea level. The millennial (500-2000-year) timescale of deep-ocean ventilation affects the timescale for natural CO2 change and thus the timescale for paleo-global climate, ice sheet, and sea level changes, but this paleo-millennial timescale should not be misinterpreted as the timescale for ice sheet response to a rapid, large, human-made climate forcing. These climate feedbacks aid interpretation of events late in the prior interglacial, when sea level rose to +6-9 m with evidence of extreme storms while Earth was less than 1 °C warmer than today. Ice melt cooling of the North Atlantic and Southern oceans increases atmospheric temperature gradients, eddy kinetic energy and baroclinicity, thus driving more powerful storms. The modeling, paleoclimate evidence, and ongoing observations together imply that 2 °C global warming above the preindustrial level could be dangerous. Continued high fossil fuel emissions this century are predicted to yield (1) cooling of the Southern Ocean, especially in the Western Hemisphere; (2) slowing of the Southern Ocean overturning circulation, warming of the ice shelves, and growing ice sheet mass loss; (3) slowdown and eventual shutdown of the Atlantic overturning circulation with cooling of the North Atlantic region; (4) increasingly powerful storms; and (5) nonlinearly growing sea level rise, reaching several meters over a timescale of 50-150 years. These predictions, especially the cooling in the Southern Ocean and North Atlantic with markedly reduced warming or even cooling in Europe, differ fundamentally from existing climate change assessments. We discuss observations and modeling studies needed to refute or clarify these assertions.

Shell Condition and Survival of Puget Sound Pteropods Are Impaired by Ocean Acidification Conditions

PubMed Central

Busch, D. Shallin; Maher, Michael; Thibodeau, Patricia; McElhany, Paul

2014-01-01

We tested whether the thecosome pteropod Limacina helicina from Puget Sound, an urbanized estuary in the northwest continental US, experiences shell dissolution and altered mortality rates when exposed to the high CO2, low aragonite saturation state (Ωa) conditions that occur in Puget Sound and the northeast Pacific Ocean. Five, week-long experiments were conducted in which we incubated pteropods collected from Puget Sound in four carbon chemistry conditions: current summer surface (∼460–500 µatm CO2, Ωa≈1.59), current deep water or surface conditions during upwelling (∼760 and ∼1600–1700 µatm CO2, Ωa≈1.17 and 0.56), and future deep water or surface conditions during upwelling (∼2800–3400 µatm CO2, Ωa≈0.28). We measured shell condition using a scoring regime of five shell characteristics that capture different aspects of shell dissolution. We characterized carbon chemistry conditions in statistical analyses with Ωa, and conducted analyses considering Ωa both as a continuous dataset and as discrete treatments. Shell dissolution increased linearly as aragonite saturation state decreased. Discrete treatment comparisons indicate that shell dissolution was greater in undersaturated treatments compared to oversaturated treatments. Survival increased linearly with aragonite saturation state, though discrete treatment comparisons indicated that survival was similar in all but the lowest saturation state treatment. These results indicate that, under starvation conditions, pteropod survival may not be greatly affected by current and expected near-future aragonite saturation state in the NE Pacific, but shell dissolution may. Given that subsurface waters in Puget Sound’s main basin are undersaturated with respect to aragonite in the winter and can be undersaturated in the summer, the condition and persistence of the species in this estuary warrants further study. PMID:25162395

Shell condition and survival of Puget Sound pteropods are impaired by ocean acidification conditions.

PubMed

Busch, D Shallin; Maher, Michael; Thibodeau, Patricia; McElhany, Paul

2014-01-01

We tested whether the thecosome pteropod Limacina helicina from Puget Sound, an urbanized estuary in the northwest continental US, experiences shell dissolution and altered mortality rates when exposed to the high CO2, low aragonite saturation state (Ωa) conditions that occur in Puget Sound and the northeast Pacific Ocean. Five, week-long experiments were conducted in which we incubated pteropods collected from Puget Sound in four carbon chemistry conditions: current summer surface (∼460-500 µatm CO2, Ωa≈1.59), current deep water or surface conditions during upwelling (∼760 and ∼1600-1700 µatm CO2, Ωa≈1.17 and 0.56), and future deep water or surface conditions during upwelling (∼2800-3400 µatm CO2, Ωa≈0.28). We measured shell condition using a scoring regime of five shell characteristics that capture different aspects of shell dissolution. We characterized carbon chemistry conditions in statistical analyses with Ωa, and conducted analyses considering Ωa both as a continuous dataset and as discrete treatments. Shell dissolution increased linearly as aragonite saturation state decreased. Discrete treatment comparisons indicate that shell dissolution was greater in undersaturated treatments compared to oversaturated treatments. Survival increased linearly with aragonite saturation state, though discrete treatment comparisons indicated that survival was similar in all but the lowest saturation state treatment. These results indicate that, under starvation conditions, pteropod survival may not be greatly affected by current and expected near-future aragonite saturation state in the NE Pacific, but shell dissolution may. Given that subsurface waters in Puget Sound's main basin are undersaturated with respect to aragonite in the winter and can be undersaturated in the summer, the condition and persistence of the species in this estuary warrants further study.

Early detection of ocean acidification effects on marine calcification

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ilyina, T.; Zeebe, R. E.; E. Maier-Reimer

Ocean acidification is likely to impact calcification rates in many pelagic organisms, which may in turn cause significant changes in marine ecosystem structure. We examine effects of changes in marine CaCO3 production on total alkalinity (TA) in the ocean using the global biogeochemical ocean model HAMOCC. We test a variety of future calcification scenarios because experimental studies with different organisms have revealed a wide range of calcification sensitivities to CaCO3 saturation state. The model integrations start at a preindustrial steady state in the year 1800 and run until the year 2300 forced with anthropogenic CO2 emissions. Calculated trends in TAmore » are evaluated taking into account the natural variability in ocean carbonate chemistry, as derived from repeat hydrographic transects. We conclude that the data currently available does not allow discerning significant trends in TA due to changes in pelagic calcification caused by ocean acidification. Given different calcification scenarios, our model calculations indicate that the TA increase over time will start being detectable by the year 2040, increasing by 5–30 umol/kg compared to the present-day values. In a scenario of extreme reductions in calcification, large TA changes relative to preindustrial conditions would have occurred at present, which we consider very unlikely. However, the time interval of reliable TA observations is too short to disregard this scenario. The largest increase in surface ocean TA is predicted for the tropical and subtropical regions. In order to monitor and quantify possible early signs of acidification effects, we suggest to specifically target those regions during future ocean chemistry surveys.« less

Effects of ocean acidification on the potency of macroalgal allelopathy to a common coral

PubMed Central

Del Monaco, Carlos; Hay, Mark E.; Gartrell, Patrick; Mumby, Peter J.; Diaz-Pulido, Guillermo

2017-01-01

Many coral reefs have phase shifted from coral to macroalgal dominance. Ocean acidification (OA) due to elevated CO2 is hypothesised to advantage macroalgae over corals, contributing to these shifts, but the mechanisms affecting coral-macroalgal interactions under OA are unknown. Here, we show that (i) three common macroalgae are more damaging to a common coral when they compete under CO2 concentrations predicted to occur in 2050 and 2100 than under present-day conditions, (ii) that two macroalgae damage corals via allelopathy, and (iii) that one macroalga is allelopathic under conditions of elevated CO2, but not at ambient levels. Lipid-soluble, surface extracts from the macroalga Canistrocarpus (=Dictyota) cervicornis were significantly more damaging to the coral Acropora intermedia growing in the field if these extracts were from thalli grown under elevated vs ambient concentrations of CO2. Extracts from the macroalgae Chlorodesmis fastigiata and Amansia glomerata were not more potent when grown under elevated CO2. Our results demonstrate increasing OA advantages seaweeds over corals, that algal allelopathy can mediate coral-algal interactions, and that OA may enhance the allelopathy of some macroalgae. Other mechanisms also affect coral-macroalgal interactions under OA, and OA further suppresses the resilience of coral reefs suffering blooms of macroalgae. PMID:28145458

Effects of ocean acidification on the potency of macroalgal allelopathy to a common coral.

PubMed

Del Monaco, Carlos; Hay, Mark E; Gartrell, Patrick; Mumby, Peter J; Diaz-Pulido, Guillermo

2017-02-01

Many coral reefs have phase shifted from coral to macroalgal dominance. Ocean acidification (OA) due to elevated CO 2 is hypothesised to advantage macroalgae over corals, contributing to these shifts, but the mechanisms affecting coral-macroalgal interactions under OA are unknown. Here, we show that (i) three common macroalgae are more damaging to a common coral when they compete under CO 2 concentrations predicted to occur in 2050 and 2100 than under present-day conditions, (ii) that two macroalgae damage corals via allelopathy, and (iii) that one macroalga is allelopathic under conditions of elevated CO 2 , but not at ambient levels. Lipid-soluble, surface extracts from the macroalga Canistrocarpus (=Dictyota) cervicornis were significantly more damaging to the coral Acropora intermedia growing in the field if these extracts were from thalli grown under elevated vs ambient concentrations of CO 2 . Extracts from the macroalgae Chlorodesmis fastigiata and Amansia glomerata were not more potent when grown under elevated CO 2 . Our results demonstrate increasing OA advantages seaweeds over corals, that algal allelopathy can mediate coral-algal interactions, and that OA may enhance the allelopathy of some macroalgae. Other mechanisms also affect coral-macroalgal interactions under OA, and OA further suppresses the resilience of coral reefs suffering blooms of macroalgae.

Effects of ocean acidification on the potency of macroalgal allelopathy to a common coral

NASA Astrophysics Data System (ADS)

Del Monaco, Carlos; Hay, Mark E.; Gartrell, Patrick; Mumby, Peter J.; Diaz-Pulido, Guillermo

2017-02-01

Many coral reefs have phase shifted from coral to macroalgal dominance. Ocean acidification (OA) due to elevated CO2 is hypothesised to advantage macroalgae over corals, contributing to these shifts, but the mechanisms affecting coral-macroalgal interactions under OA are unknown. Here, we show that (i) three common macroalgae are more damaging to a common coral when they compete under CO2 concentrations predicted to occur in 2050 and 2100 than under present-day conditions, (ii) that two macroalgae damage corals via allelopathy, and (iii) that one macroalga is allelopathic under conditions of elevated CO2, but not at ambient levels. Lipid-soluble, surface extracts from the macroalga Canistrocarpus (=Dictyota) cervicornis were significantly more damaging to the coral Acropora intermedia growing in the field if these extracts were from thalli grown under elevated vs ambient concentrations of CO2. Extracts from the macroalgae Chlorodesmis fastigiata and Amansia glomerata were not more potent when grown under elevated CO2. Our results demonstrate increasing OA advantages seaweeds over corals, that algal allelopathy can mediate coral-algal interactions, and that OA may enhance the allelopathy of some macroalgae. Other mechanisms also affect coral-macroalgal interactions under OA, and OA further suppresses the resilience of coral reefs suffering blooms of macroalgae.

Clathrate hydrate stability models for Titan: implications for a global subsurface ocean

NASA Astrophysics Data System (ADS)

Basu Sarkar, D.; Elwood Madden, M.

2013-12-01

Titan is the only planetary body in the solar system, apart from the Earth, with liquid at its surface. Titan's changing rotational period suggests that a global subsurface ocean decouples the icy crust from the interior. Several studies predict the existence of such an internal ocean below an Ice I layer, ranging in depth between a few tens of kilometers to a few hundreds of kilometers, depending on the composition of the icy crust and liquid-ocean. While the overall density of Titan is well constrained, the degree of differentiation within the interior is unclear. These uncertainties lead to poor understanding of the volatile content of the moon. However, unlike other similar large icy moons like Ganymede and Callisto, Titan has a thick nitrogen atmosphere, with methane as the second most abundant constituent - 5% near the surface. Titan's atmosphere, surface, and interior are likely home to various compounds such as C2H6, CO2, Ar, N2 and CH4, capable of forming clathrate hydrates. In addition, the moon has low temperature and low-to-high pressure conditions required for clathrate formation. Therefore the occurrence of extensive multicomponent hydrates may effect the composition of near-surface materials, the subsurface ocean, as well as the atmosphere. This work uses models of hydrate stability for a number of plausible hydrate formers including CH4, C2H6, CH4 + C2H6 and CH4 + NH3, and equilibrium geothermal gradients for probable near-surface materials to delineate the lateral and vertical extent of clathrate hydrate stability zones for Titan. By comparing geothermal gradients with clathrate stability fields for these systems we investigate possible compositions of Titan's global subsurface ocean. Preliminary model results indicate that ethane hydrates or compound hydrates of ethane and methane could be destabilized within the proposed depth range of the internal ocean, while methane/ammonia or pure methane hydrates may not be affected. Therefore, ethane or ethane-methane clathrates may be a major component of Titan's icy shell. Modeled geothermal gradients and stability fields of possible clathrate formers with three different scenarios for an internal ocean from the recent literature. Geothermal gradients obtained from thermal conductivity and density representing water ice and pure CH4-C2H6 hydrate. Clathrate stability field determined using HYDOFF and recent publications of NH3 clathrate stability.

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

NASA Astrophysics Data System (ADS)

Goyet, C.; Touratier, F.

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

Coral Reefs and People in a High-CO2 World: Where Can Science Make a Difference to People?

PubMed Central

Langdon, Chris; Ekstrom, Julia A.; Cooley, Sarah R.; Suatoni, Lisa; Beck, Michael W.; Brander, Luke M.; Burke, Lauretta; Cinner, Josh E.; Doherty, Carolyn; Edwards, Peter E. T.; Gledhill, Dwight; Jiang, Li-Qing; van Hooidonk, Ruben J.; Teh, Louise; Waldbusser, George G.; Ritter, Jessica

2016-01-01

Reefs and People at Risk Increasing levels of carbon dioxide in the atmosphere put shallow, warm-water coral reef ecosystems, and the people who depend upon them at risk from two key global environmental stresses: 1) elevated sea surface temperature (that can cause coral bleaching and related mortality), and 2) ocean acidification. These global stressors: cannot be avoided by local management, compound local stressors, and hasten the loss of ecosystem services. Impacts to people will be most grave where a) human dependence on coral reef ecosystems is high, b) sea surface temperature reaches critical levels soonest, and c) ocean acidification levels are most severe. Where these elements align, swift action will be needed to protect people’s lives and livelihoods, but such action must be informed by data and science. An Indicator Approach Designing policies to offset potential harm to coral reef ecosystems and people requires a better understanding of where CO2-related global environmental stresses could cause the most severe impacts. Mapping indicators has been proposed as a way of combining natural and social science data to identify policy actions even when the needed science is relatively nascent. To identify where people are at risk and where more science is needed, we map indicators of biological, physical and social science factors to understand how human dependence on coral reef ecosystems will be affected by globally-driven threats to corals expected in a high-CO2 world. Western Mexico, Micronesia, Indonesia and parts of Australia have high human dependence and will likely face severe combined threats. As a region, Southeast Asia is particularly at risk. Many of the countries most dependent upon coral reef ecosystems are places for which we have the least robust data on ocean acidification. These areas require new data and interdisciplinary scientific research to help coral reef-dependent human communities better prepare for a high CO2 world. PMID:27828972

Coral Reefs and People in a High-CO2 World: Where Can Science Make a Difference to People?

PubMed

Pendleton, Linwood; Comte, Adrien; Langdon, Chris; Ekstrom, Julia A; Cooley, Sarah R; Suatoni, Lisa; Beck, Michael W; Brander, Luke M; Burke, Lauretta; Cinner, Josh E; Doherty, Carolyn; Edwards, Peter E T; Gledhill, Dwight; Jiang, Li-Qing; van Hooidonk, Ruben J; Teh, Louise; Waldbusser, George G; Ritter, Jessica

2016-01-01

Increasing levels of carbon dioxide in the atmosphere put shallow, warm-water coral reef ecosystems, and the people who depend upon them at risk from two key global environmental stresses: 1) elevated sea surface temperature (that can cause coral bleaching and related mortality), and 2) ocean acidification. These global stressors: cannot be avoided by local management, compound local stressors, and hasten the loss of ecosystem services. Impacts to people will be most grave where a) human dependence on coral reef ecosystems is high, b) sea surface temperature reaches critical levels soonest, and c) ocean acidification levels are most severe. Where these elements align, swift action will be needed to protect people's lives and livelihoods, but such action must be informed by data and science. Designing policies to offset potential harm to coral reef ecosystems and people requires a better understanding of where CO2-related global environmental stresses could cause the most severe impacts. Mapping indicators has been proposed as a way of combining natural and social science data to identify policy actions even when the needed science is relatively nascent. To identify where people are at risk and where more science is needed, we map indicators of biological, physical and social science factors to understand how human dependence on coral reef ecosystems will be affected by globally-driven threats to corals expected in a high-CO2 world. Western Mexico, Micronesia, Indonesia and parts of Australia have high human dependence and will likely face severe combined threats. As a region, Southeast Asia is particularly at risk. Many of the countries most dependent upon coral reef ecosystems are places for which we have the least robust data on ocean acidification. These areas require new data and interdisciplinary scientific research to help coral reef-dependent human communities better prepare for a high CO2 world.

How to Sustain Warm Northern High Latitudes during the Late Pliocene? Roles of CO2, Orbital Changes and Increased Mediterranean Salinity on Oceanic Circulation

NASA Astrophysics Data System (ADS)

Contoux, C.; Zhang, Z.; Li, C.; Nisancioglu, K. H.; Risebrobakken, B.

2014-12-01

Northern high latitudes are thought to have been especially warm during the late Pliocene (e.g. Dowsett et al., 2013). However, the mechanisms sustaining these warm high latitude conditions are debated, especially because warm high latitudes are not necessarily depending on a stronger AMOC (Zhang et al., 2013). On the global scale, several authors reported CO2 level variability during the Pliocene ranging from 280 ppm to 450 ppm (e.g. Badger et al., 2013), which could be linked with orbital variability. More regionally, an aridification of the Mediterranean region is thought to have increased the Mediterranean outflow during the same period (e.g. Khélifi et al., 2009). These different forcings must have impacted on salinity and temperature profiles in the North Atlantic/Arctic oceans, which are then recorded at the local scale in the proxies derived from sediment cores. In order to carefully interpret these proxies, it is necessary to understand the large scale dynamics of the region during that period and its potential maximum variability with CO2 and orbital changes as well as Mediterranean outflow increase. Using the NorESM-L coupled atmosphere ocean model, which has a refined oceanic grid in the Nordic Seas region, we investigate the roles of extreme CO2and orbital variability on the Atlantic and Arctic oceanic circulation. An additional test to higher salinity in the Mediterranean is carried out. This study is part of a larger project which aims at characterising the state of the Nordic Seas during the Pliocene, and includes multi-proxy reconstructions and sensitivity model studies. References Badger et al., 2013. High resolution alkenone palaeobarometry indicates relatively stable pCO2 during the Pliocene (3.3 - 2.8 Ma), Philosophical Transactions of the Royal Society A, 371, 20130094. Dowsett et al., 2013. Sea surface temperature of the mid-Piacenzian ocean: a data-model comparison, Nature Scientific Reports, 3, 2013, doi:10.1038/srep02013. Khélifi et al., 2009. A major and long term intensification of the Mediterranean outflow water, 3.5 - 3.3 Ma ago, Geology, 2009,37;811-814, doi: 10.1130/G30058A.1 Zhang, Z.-S. et al., 2013. Mid-pliocene Atlantic meridional overturning circulation not unlike modern, Clim. Past, 9, 1495--1504, doi:10.5194/cp-9-1495-2013.

The young sun, the early earth and the photochemistry of oxygen, ozone and formaldehyde in the early atmosphere

NASA Technical Reports Server (NTRS)

Canuto, V. M.; Levine, J. S.; Augustsson, T. R.; Imhoff, C. L.; Goldman, I.; Hubickyj, O.

1986-01-01

Recent work on the evolution of the solar nebula and the subsequent formation of planets is reviewed, and the stages of star formation thought to lead to a protosun and an accompanying solar nebula are considered. Photochemical results suggest that concentrations of O2, O3, and H2CO, and the ratio of CO/CO2 in the prebiological paleoatmosphere are very sensitive to atmospheric levels of H2O and CO2 and to the flux of incident solar ultraviolet. For enhanced levels of CO2 and solar UV, surface levels of O2 may have approached the parts per billion level in the prebiological paleoatmosphere. It is suggested that 10 percent or more of the enhanced H2CO production could have been rained out of the atmosphere into the early oceans where synthesis into more complex organic molecules could have taken place. CO/CO2 values of greater than unity could have been possible for enhanced levels of solar UV flux.

The influence of oceanic basins on drought and ecosystem dynamics in Northeast Brazil

NASA Astrophysics Data System (ADS)

Santos Pereira, Marcos Paulo; Justino, Flavio; Mendes Malhado, Ana Claudia; Barbosa, Humberto; Marengo, José

2014-12-01

The 2012 drought in Northeast Brazil was the harshest in decades, with potentially significant impacts on the vegetation of the unique semi-arid caatinga biome and on local livelihoods. Here, we use a coupled climate-vegetation model (CCM3-IBIS) to: (1) investigate the role of the Pacific and Atlantic oceans in the 2012 drought, and; (2) evaluate the response of the caatinga vegetation to the 2012 climate extreme. Our results indicate that anomalous sea surface temperatures (SSTs) in the Atlantic Ocean were the primary factor forcing the 2012 drought, with Pacific Ocean SST having a larger role in sustaining typical climatic conditions in the region. The drought strongly influenced net primary production in the caatinga, causing a reduction in annual net ecosystem exchange indicating a reduction in amount of CO2 released to the atmosphere.

Responses of the deep ocean carbonate system to carbon reorganization during the Last Glacial-interglacial cycle

NASA Astrophysics Data System (ADS)

Yu, Jimin; Anderson, Robert F.; Jin, Zhangdong; Rae, James W. B.; Opdyke, Bradley N.; Eggins, Stephen M.

2013-09-01

We present new deep water carbonate ion concentration ([CO32-]) records, reconstructed using Cibicidoides wuellerstorfi B/Ca, for one core from Caribbean Basin (water depth = 3623 m, sill depth = 1.8 km) and three cores located at 2.3-4.3 km water depth from the equatorial Pacific Ocean during the Last Glacial-interglacial cycle. The pattern of deep water [CO32-] in the Caribbean Basin roughly mirrors that of atmospheric CO2, reflecting a dominant influence from preformed [CO32-] in the North Atlantic Ocean. Compared to the amplitude of ˜65 μmol/kg in the deep Caribbean Basin, deep water [CO32-] in the equatorial Pacific Ocean has varied by no more than ˜15 μmol/kg due to effective buffering of CaCO3 on deep-sea pH in the Pacific Ocean. Our results suggest little change in the global mean deep ocean [CO32-] between the Last Glacial Maximum (LGM) and the Late Holocene. The three records from the Pacific Ocean show long-term increases in [CO32-] by ˜7 μmol/kg from Marine Isotope Stage (MIS) 5c to mid MIS 3, consistent with the response of the deep ocean carbonate system to a decline in neritic carbonate production associated with ˜60 m drop in sea-level (the “coral-reef” hypothesis). Superimposed upon the long-term trend, deep water [CO32-] in the Pacific Ocean displays transient changes, which decouple with δ13C in the same cores, at the start and end of MIS 4. These changes in [CO32-] and δ13C are consistent with what would be expected from vertical nutrient fractionation and carbonate compensation. The observed ˜4 μmol/kg [CO32-] decline in the two Pacific cores at >3.4 km water depth from MIS 3 to the LGM indicate further strengthening of deep ocean stratification, which contributed to the final step of atmospheric CO2 drawdown during the last glaciation. The striking similarity between deep water [CO32-] and 230Th-normalized CaCO3 flux at two adjacent sites from the central equatorial Pacific Ocean provides convincing evidence that deep-sea carbonate dissolution dominantly controlled CaCO3 preservation at these sites in the past. Our results offer new and quantitative constraints from deep ocean carbonate chemistry to understand roles of various mechanisms in atmospheric CO2 changes over the Last Glacial-interglacial cycle.

In situ Raman-based measurements of high dissolved methane concentrations in hydrate-rich ocean sediments

NASA Astrophysics Data System (ADS)

Zhang, Xin; Hester, Keith C.; Ussler, William; Walz, Peter M.; Peltzer, Edward T.; Brewer, Peter G.

2011-04-01

Ocean sediment dissolved CH4 concentrations are of interest for possible climate-driven venting from sea floor hydrate decomposition, for supporting the large-scale microbial anaerobic oxidation of CH4 that holds the oceanic CH4 budget in balance, and for environmental issues of the oil and gas industry. Analyses of CH4 from recovered cores near vent locations typically show a maximum of ˜1 mM, close to the 1 atmosphere equilibrium value. We show from novel in situ measurement with a Raman-based probe that geochemically coherent profiles of dissolved CH4 occur rising to 30 mM (pCH4 = 3 MPa) or an excess pressure ˜3× greater than CO2 in a bottle of champagne. Normalization of the CH4 Raman ν1 peak to the ubiquitous water ν2 bending peak provides a fundamental internal calibration. Very large losses of CH4 and fractions of other gases (CO2, H2S) must typically occur from recovered cores at gas rich sites. The new data are consistent with observations of microbial biomass and observed CH4 oxidation rates at hydrate rich sites and support estimates of a greatly expanded near surface oceanic pore water CH4 reservoir.

NOAA's Role in Sustaining Global Ocean Observations: Future Plans for OAR's Ocean Observing and Monitoring Division

NASA Astrophysics Data System (ADS)

Todd, James; Legler, David; Piotrowicz, Stephen; Raymond, Megan; Smith, Emily; Tedesco, Kathy; Thurston, Sidney

2017-04-01

The Ocean Observing and Monitoring Division (OOMD, formerly the Climate Observation Division) of the National Oceanic and Atmospheric Administration (NOAA) Climate Program Office provides long-term, high-quality global observations, climate information and products for researchers, forecasters, assessments and other users of environmental information. In this context, OOMD-supported activities serve a foundational role in an enterprise that aims to advance 1) scientific understanding, 2) monitoring and prediction of climate and 3) understanding of potential impacts to enable a climate resilient society. Leveraging approximately 50% of the Global Ocean Observing System, OOMD employs an internationally-coordinated, multi-institution global strategy that brings together data from multiple platforms including surface drifting buoys, Argo profiling floats, flux/transport moorings (RAMA, PIRATA, OceanSITES), GLOSS tide gauges, SOOP-XBT and SOOP-CO2, ocean gliders and repeat hydrographic sections (GO-SHIP). OOMD also engages in outreach, education and capacity development activities to deliver training on the social-economic applications of ocean data. This presentation will highlight recent activities and plans for 2017 and beyond.

Shotgun proteomics reveals physiological response to ocean acidification in Crassostrea gigas.

PubMed

Timmins-Schiffman, Emma; Coffey, William D; Hua, Wilber; Nunn, Brook L; Dickinson, Gary H; Roberts, Steven B

2014-11-03

Ocean acidification as a result of increased anthropogenic CO2 emissions is occurring in marine and estuarine environments worldwide. The coastal ocean experiences additional daily and seasonal fluctuations in pH that can be lower than projected end-of-century open ocean pH reductions. In order to assess the impact of ocean acidification on marine invertebrates, Pacific oysters (Crassostrea gigas) were exposed to one of four different p CO2 levels for four weeks: 400 μatm (pH 8.0), 800 μatm (pH 7.7), 1000 μatm (pH 7.6), or 2800 μatm (pH 7.3). At the end of the four week exposure period, oysters in all four p CO2 environments deposited new shell, but growth rate was not different among the treatments. However, micromechanical properties of the new shell were compromised by elevated p CO2. Elevated p CO2 affected neither whole body fatty acid composition, nor glycogen content, nor mortality rate associated with acute heat shock. Shotgun proteomics revealed that several physiological pathways were significantly affected by ocean acidification, including antioxidant response, carbohydrate metabolism, and transcription and translation. Additionally, the proteomic response to a second stress differed with p CO2, with numerous processes significantly affected by mechanical stimulation at high versus low p CO2 (all proteomics data are available in the ProteomeXchange under the identifier PXD000835). Oyster physiology is significantly altered by exposure to elevated p CO2, indicating changes in energy resource use. This is especially apparent in the assessment of the effects of p CO2 on the proteomic response to a second stress. The altered stress response illustrates that ocean acidification may impact how oysters respond to other changes in their environment. These data contribute to an integrative view of the effects of ocean acidification on oysters as well as physiological trade-offs during environmental stress.

Ocean acidification exerts negative effects during warming conditions in a developing Antarctic fish

PubMed Central

Flynn, Erin E; Bjelde, Brittany E; Miller, Nathan A

2015-01-01

Abstract Anthropogenic CO2 is rapidly causing oceans to become warmer and more acidic, challenging marine ectotherms to respond to simultaneous changes in their environment. While recent work has highlighted that marine fishes, particularly during early development, can be vulnerable to ocean acidification, we lack an understanding of how life-history strategies, ecosystems and concurrent ocean warming interplay with interspecific susceptibility. To address the effects of multiple ocean changes on cold-adapted, slowly developing fishes, we investigated the interactive effects of elevated partial pressure of carbon dioxide (pCO2) and temperature on the embryonic physiology of an Antarctic dragonfish (Gymnodraco acuticeps), with protracted embryogenesis (∼10 months). Using an integrative, experimental approach, our research examined the impacts of near-future warming [−1 (ambient) and 2°C (+3°C)] and ocean acidification [420 (ambient), 650 (moderate) and 1000 μatm pCO2 (high)] on survival, development and metabolic processes over the course of 3 weeks in early development. In the presence of increased pCO2 alone, embryonic mortality did not increase, with greatest overall survival at the highest pCO2. Furthermore, embryos were significantly more likely to be at a later developmental stage at high pCO2 by 3 weeks relative to ambient pCO2. However, in combined warming and ocean acidification scenarios, dragonfish embryos experienced a dose-dependent, synergistic decrease in survival and developed more slowly. We also found significant interactions between temperature, pCO2 and time in aerobic enzyme activity (citrate synthase). Increased temperature alone increased whole-organism metabolic rate (O2 consumption) and developmental rate and slightly decreased osmolality at the cost of increased mortality. Our findings suggest that developing dragonfish are more sensitive to ocean warming and may experience negative physiological effects of ocean acidification only in the presence of an increased temperature. In addition to reduced hatching success, alterations in development and metabolism due to ocean warming and acidification could have negative ecological consequences owing to changes in phenology (i.e. early hatching) in the highly seasonal Antarctic ecosystem. PMID:27293718

Ocean acidification exerts negative effects during warming conditions in a developing Antarctic fish.

PubMed

Flynn, Erin E; Bjelde, Brittany E; Miller, Nathan A; Todgham, Anne E

2015-01-01

Anthropogenic CO2 is rapidly causing oceans to become warmer and more acidic, challenging marine ectotherms to respond to simultaneous changes in their environment. While recent work has highlighted that marine fishes, particularly during early development, can be vulnerable to ocean acidification, we lack an understanding of how life-history strategies, ecosystems and concurrent ocean warming interplay with interspecific susceptibility. To address the effects of multiple ocean changes on cold-adapted, slowly developing fishes, we investigated the interactive effects of elevated partial pressure of carbon dioxide (pCO2) and temperature on the embryonic physiology of an Antarctic dragonfish (Gymnodraco acuticeps), with protracted embryogenesis (∼10 months). Using an integrative, experimental approach, our research examined the impacts of near-future warming [-1 (ambient) and 2°C (+3°C)] and ocean acidification [420 (ambient), 650 (moderate) and 1000 μatm pCO2 (high)] on survival, development and metabolic processes over the course of 3 weeks in early development. In the presence of increased pCO2 alone, embryonic mortality did not increase, with greatest overall survival at the highest pCO2. Furthermore, embryos were significantly more likely to be at a later developmental stage at high pCO2 by 3 weeks relative to ambient pCO2. However, in combined warming and ocean acidification scenarios, dragonfish embryos experienced a dose-dependent, synergistic decrease in survival and developed more slowly. We also found significant interactions between temperature, pCO2 and time in aerobic enzyme activity (citrate synthase). Increased temperature alone increased whole-organism metabolic rate (O2 consumption) and developmental rate and slightly decreased osmolality at the cost of increased mortality. Our findings suggest that developing dragonfish are more sensitive to ocean warming and may experience negative physiological effects of ocean acidification only in the presence of an increased temperature. In addition to reduced hatching success, alterations in development and metabolism due to ocean warming and acidification could have negative ecological consequences owing to changes in phenology (i.e. early hatching) in the highly seasonal Antarctic ecosystem.

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

NASA Astrophysics Data System (ADS)

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

2018-03-01

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

Major cellular and physiological impacts of ocean acidification on a reef building coral.

PubMed

Kaniewska, Paulina; Campbell, Paul R; Kline, David I; Rodriguez-Lanetty, Mauricio; Miller, David J; Dove, Sophie; Hoegh-Guldberg, Ove

2012-01-01

As atmospheric levels of CO(2) increase, reef-building corals are under greater stress from both increased sea surface temperatures and declining sea water pH. To date, most studies have focused on either coral bleaching due to warming oceans or declining calcification due to decreasing oceanic carbonate ion concentrations. Here, through the use of physiology measurements and cDNA microarrays, we show that changes in pH and ocean chemistry consistent with two scenarios put forward by the Intergovernmental Panel on Climate Change (IPCC) drive major changes in gene expression, respiration, photosynthesis and symbiosis of the coral, Acropora millepora, before affects on biomineralisation are apparent at the phenotype level. Under high CO(2) conditions corals at the phenotype level lost over half their Symbiodinium populations, and had a decrease in both photosynthesis and respiration. Changes in gene expression were consistent with metabolic suppression, an increase in oxidative stress, apoptosis and symbiont loss. Other expression patterns demonstrate upregulation of membrane transporters, as well as the regulation of genes involved in membrane cytoskeletal interactions and cytoskeletal remodeling. These widespread changes in gene expression emphasize the need to expand future studies of ocean acidification to include a wider spectrum of cellular processes, many of which may occur before impacts on calcification.

Major Cellular and Physiological Impacts of Ocean Acidification on a Reef Building Coral

PubMed Central

Kaniewska, Paulina; Campbell, Paul R.; Kline, David I.; Rodriguez-Lanetty, Mauricio; Miller, David J.

2012-01-01

As atmospheric levels of CO2 increase, reef-building corals are under greater stress from both increased sea surface temperatures and declining sea water pH. To date, most studies have focused on either coral bleaching due to warming oceans or declining calcification due to decreasing oceanic carbonate ion concentrations. Here, through the use of physiology measurements and cDNA microarrays, we show that changes in pH and ocean chemistry consistent with two scenarios put forward by the Intergovernmental Panel on Climate Change (IPCC) drive major changes in gene expression, respiration, photosynthesis and symbiosis of the coral, Acropora millepora, before affects on biomineralisation are apparent at the phenotype level. Under high CO2 conditions corals at the phenotype level lost over half their Symbiodinium populations, and had a decrease in both photosynthesis and respiration. Changes in gene expression were consistent with metabolic suppression, an increase in oxidative stress, apoptosis and symbiont loss. Other expression patterns demonstrate upregulation of membrane transporters, as well as the regulation of genes involved in membrane cytoskeletal interactions and cytoskeletal remodeling. These widespread changes in gene expression emphasize the need to expand future studies of ocean acidification to include a wider spectrum of cellular processes, many of which may occur before impacts on calcification. PMID:22509341

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

NASA Astrophysics Data System (ADS)

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

2016-02-01

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

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kashgarian, M; Guilderson, T P

We utilize monthly {sup 14}C data derived from coral archives in conjunction with ocean circulation models to address two questions: (1) how does the shallow circulation of the tropical Pacific vary on seasonal to decadal time scales and (2) which dynamic processes determine the mean vertical structure of the equatorial Pacific thermocline. Our results directly impact the understanding of global climate events such as the El Nino-Southern Oscillation (ENSO). To study changes in ocean circulation and water mass distribution involved in the genesis and evolution of ENSO and decadal climate variability, it is necessary to have records of climate variablesmore » several decades in length. Continuous instrumental records are limited because technology for continuous monitoring of ocean currents (e.g. satellites and moored arrays) has only recently been available, and ships of opportunity archives such as COADS contain large spatial and temporal biases. In addition, temperature and salinity in surface waters are not conservative and thus can not be independently relied upon to trace water masses, reducing the utility of historical observations. Radiocarbon in sea water is a quasi-conservative water mass tracer and is incorporated into coral skeletal material, thus coral {sup 14}C records can be used to reconstruct changes in shallow circulation that would be difficult to characterize using instrumental data. High resolution {Delta}{sup 14}C timeseries such as ours, provide a powerful constraint on the rate of surface ocean mixing and hold great promise to augment one time oceanographic surveys. {Delta}{sup 14}C timeseries such as these, not only provide fundamental information about the shallow circulation of the Pacific, but can also be directly used as a benchmark for the next generation of high resolution ocean models used in prognosticating climate. The measurement of {Delta}{sup 14}C in biological archives such as tree rings and coral growth bands is a direct record of the invasion of fossil fuel CO{sub 2} and bomb {sup 14}C into the atmosphere and surface oceans. Therefore the {Delta}{sup 14}C data that are produced in this study can be used to validate the ocean uptake of fossil fuel CO2 in coupled ocean-atmosphere models. This study takes advantage of the quasi-conservative nature of {sup 14}C as a water mass tracer by using {Delta}{sup 14}C time series in corals to identify changes in the shallow circulation of the Pacific. Although the data itself provides fundamental information on surface water mass movement the true strength is a combined approach which is greater than the individual parts; the data helps uncover deficiencies in ocean circulation models and the model results place long {Delta}{sup 14}C time series in a dynamic framework which helps to identify those locations where additional observations are most needed.« less

The Aquarius Mission: Sea Surface Salinity from Space

NASA Technical Reports Server (NTRS)

Koblinsky, Chester; Chao, Y.; deCharon, A.; Edelstein, W.; Hildebrand, P.; Lagerloef, G.; LeVine, D.; Pellerano, F.; Rahmat-Samii, Y.; Ruf, C.

2001-01-01

Aquarius is a new satellite mission concept to study the impact of the global water cycle on the ocean, including the response of the ocean to buoyancy forcing and the subsequent feedback of the ocean on the climate. The measurement objective of Aquarius is sea surface salinity, which reflects the concentration of freshwater at the ocean surface. Salinity affects the dielectric constant of sea water and, consequently, the radiometric emission of the sea surface to space. Rudimentary space observations with an L-band radiometer were first made from Skylab in the mid-70s and numerous aircraft missions of increasing quality and improved technology have been conducted since then. Technology is now available to carry out a global mission, which includes both an accurate L band (1.413 Ghz) radiometer and radar system in space and a global array of in situ observations for calibration and validation, in order to address key NASA Earth Science Enterprise questions about the global cycling of water and the response of the ocean circulation to climate change. The key scientific objectives of Aquarius examine the cycling of water at the ocean's surface, the response of the ocean circulation to buoyancy forcing, and the impact of buoyancy forcing on the ocean's thermal feedback to the climate. Global surface salinity will also improve our ability to model the surface solubility chemistry needed to estimate the air-sea exchange of CO2. In order to meet these science objectives, the NASA Salinity Sea Ice Working Group over the past three years has concluded that the mission measurement goals should be better than 0.2 practical salinity units (psu) accuracy, 100 km resolution, and weekly to revisits. The Aquarius mission proposes to meet these measurement requirements through a real aperture dual-polarized L band radiometer and radar system. This system can achieve the less than 0.1 K radiometric temperature measurement accuracy that is required. A 3 m antenna at approx. 600km altitude in a sun-synchronous orbit and 300 km swath can provide the desired 100 km resolution global coverage every week. Within this decade, it may be possible to combine satellite sea surface salinity measurements with ongoing satellite observations of temperature, surface height, air-sea fluxes; vertical profiles of temperature and salinity from the Argo program; and modern ocean/atmosphere modeling and data assimilation tools, in order to finally address the complex influence of buoyancy on the ocean circulation and climate.

Rising atmospheric CO2 leads to large impact of biology on Southern Ocean CO2 uptake via changes of the Revelle factor

PubMed Central

Hauck, J; Völker, C

2015-01-01

The Southern Ocean is a key region for global carbon uptake and is characterized by a strong seasonality with the annual CO2 uptake being mediated by biological carbon drawdown in summer. Here we show that the contribution of biology to CO2 uptake will become even more important until 2100. This is the case even if biological production remains unaltered and can be explained by the decreasing buffer capacity of the ocean as its carbon content increases. The same amount of biological carbon drawdown leads to a more than twice as large reduction in CO2(aq) concentration and hence to a larger CO2 gradient between ocean and atmosphere that drives the gas exchange. While the winter uptake south of 44°S changes little, the summer uptake increases largely and is responsible for the annual mean response. The combination of decreasing buffer capacity and strong seasonality of biological carbon drawdown introduces a strong and increasing seasonality in the anthropogenic carbon uptake. Key Points Decrease of buffer capacity leads to stronger summer CO2 uptake in the future Biology will contribute more to future CO2 uptake in Southern Ocean Seasonality affects anthropogenic carbon uptake strongly PMID:26074650

Mantle to surface degassing of carbon- and sulphur-rich alkaline magma at El Hierro, Canary Islands

NASA Astrophysics Data System (ADS)

Longpré, Marc-Antoine; Stix, John; Klügel, Andreas; Shimizu, Nobumichi

2017-02-01

Basaltic volcanoes transfer volatiles from the mantle to the surface of the Earth. The quantification of deep volatile fluxes relies heavily on estimates of the volatile content of primitive magmas, the best archive of which is provided by melt inclusions. Available data from volcanoes producing mafic alkaline lavas in a range of tectonic settings suggest high volatile fluxes, but information remains sparse, particularly for intraplate ocean islands. Here we present measurements of volatile and trace element concentrations, as well as sulphur speciation, in olivine-hosted melt inclusions and matrix glasses from quenched basanite lava balloon samples from the 2011-2012 submarine eruption at El Hierro, Canary Islands. The results reveal remarkably high concentrations of dissolved volatiles and incompatible trace elements in this magma, with ∼80 ppm Nb and up to 3420 ppm CO2, 3.0 wt.% H2O and 5080 ppm S. Reconstructed primitive CO2 contents, considering CO2/Nb systematics and possible CO2 sequestration in shrinkage bubbles, reach weight percent levels, indicating that carbon is a major constituent of Canary Island magmas at depth and that exsolution of a CO2-rich fluid begins in the mantle at pressures in excess of 1 GPa. Correlations between sulphur concentration, sulphur speciation and water content suggest strong reduction of an initially oxidised mantle magma, likely controlled by coupled H2O and S degassing. This late-stage redox change may have triggered sulphide saturation, recorded by globular sulphide inclusions in clinopyroxene and ulvöspinel. The El Hierro basanite thus had a particularly high volatile-carrying capacity and released a minimum of 1.3-2.1 Tg CO2 and 1.8-2.9 Tg S to the environment, causing substantial stress on the local submarine ecosystem. These results highlight the important contribution of alkaline ocean island volcanoes, such as the Canary Islands, to volatile fluxes from the mantle.

Effects of ocean warming and acidification on survival, growth and skeletal development in the early benthic juvenile sea urchin (Heliocidaris erythrogramma).

PubMed

Wolfe, Kennedy; Dworjanyn, Symon A; Byrne, Maria

2013-09-01

Co-occurring ocean warming, acidification and reduced carbonate mineral saturation have significant impacts on marine biota, especially calcifying organisms. The effects of these stressors on development and calcification in newly metamorphosed juveniles (ca. 0.5 mm test diameter) of the intertidal sea urchin Heliocidaris erythrogramma, an ecologically important species in temperate Australia, were investigated in context with present and projected future conditions. Habitat temperature and pH/pCO2 were documented to place experiments in a biologically and ecologically relevant context. These parameters fluctuated diurnally up to 10 °C and 0.45 pH units. The juveniles were exposed to three temperature (21, 23 and 25 °C) and four pH (8.1, 7.8, 7.6 and 7.4) treatments in all combinations, representing ambient sea surface conditions (21 °C, pH 8.1; pCO2 397; ΩCa 4.7; ΩAr 3.1), near-future projected change (+2-4 °C, -0.3-0.5 pH units; pCO2 400-1820; ΩCa 5.0-1.6; ΩAr 3.3-1.1), and extreme conditions experienced at low tide (+4 °C, -0.3-0.7 pH units; pCO2 2850-2967; ΩCa 1.1-1.0; ΩAr 0.7-0.6). The lowest pH treatment (pH 7.4) was used to assess tolerance levels. Juvenile survival and test growth were resilient to current and near-future warming and acidification. Spine development, however, was negatively affected by near-future increased temperature (+2-4 °C) and extreme acidification (pH 7.4), with a complex interaction between stressors. Near-future warming was the more significant stressor. Spine tips were dissolved in the pH 7.4 treatments. Adaptation to fluctuating temperature-pH conditions in the intertidal may convey resilience to juvenile H. erythrogramma to changing ocean conditions, however, ocean warming and acidification may shift baseline intertidal temperature and pH/pCO2 to levels that exceed tolerance limits. © 2013 John Wiley & Sons Ltd.

The O2, pH and Ca2+ Microenvironment of Benthic Foraminifera in a High CO2 World

PubMed Central

Glas, Martin S.; Fabricius, Katharina E.; de Beer, Dirk; Uthicke, Sven

2012-01-01

Ocean acidification (OA) can have adverse effects on marine calcifiers. Yet, phototrophic marine calcifiers elevate their external oxygen and pH microenvironment in daylight, through the uptake of dissolved inorganic carbon (DIC) by photosynthesis. We studied to which extent pH elevation within their microenvironments in daylight can counteract ambient seawater pH reductions, i.e. OA conditions. We measured the O2 and pH microenvironment of four photosymbiotic and two symbiont-free benthic tropical foraminiferal species at three different OA treatments (∼432, 1141 and 2151 µatm pCO2). The O2 concentration difference between the seawater and the test surface (ΔO2) was taken as a measure for the photosynthetic rate. Our results showed that O2 and pH levels were significantly higher on photosymbiotic foraminiferal surfaces in light than in dark conditions, and than on surfaces of symbiont-free foraminifera. Rates of photosynthesis at saturated light conditions did not change significantly between OA treatments (except in individuals that exhibited symbiont loss, i.e. bleaching, at elevated pCO2). The pH at the cell surface decreased during incubations at elevated pCO2, also during light incubations. Photosynthesis increased the surface pH but this increase was insufficient to compensate for ambient seawater pH decreases. We thus conclude that photosynthesis does only partly protect symbiont bearing foraminifera against OA. PMID:23166810

Temperature and CO2 additively regulate physiology, morphology and genomic responses of larval sea urchins, Strongylocentrotus purpuratus

PubMed Central

Padilla-Gamiño, Jacqueline L.; Kelly, Morgan W.; Evans, Tyler G.; Hofmann, Gretchen E.

2013-01-01

Ocean warming and ocean acidification, both consequences of anthropogenic production of CO2, will combine to influence the physiological performance of many species in the marine environment. In this study, we used an integrative approach to forecast the impact of future ocean conditions on larval purple sea urchins (Strongylocentrotus purpuratus) from the northeast Pacific Ocean. In laboratory experiments that simulated ocean warming and ocean acidification, we examined larval development, skeletal growth, metabolism and patterns of gene expression using an orthogonal comparison of two temperature (13°C and 18°C) and pCO2 (400 and 1100 μatm) conditions. Simultaneous exposure to increased temperature and pCO2 significantly reduced larval metabolism and triggered a widespread downregulation of histone encoding genes. pCO2 but not temperature impaired skeletal growth and reduced the expression of a major spicule matrix protein, suggesting that skeletal growth will not be further inhibited by ocean warming. Importantly, shifts in skeletal growth were not associated with developmental delay. Collectively, our results indicate that global change variables will have additive effects that exceed thresholds for optimized physiological performance in this keystone marine species. PMID:23536595

GOSAT and OCO-2 Inter-comparison on Measured Spectral Radiance and Retrieved Carbon Dioxide

NASA Astrophysics Data System (ADS)

Kataoka, F.; Kuze, A.; Shiomi, K.; Suto, H.; Crisp, D.; Bruegge, C. J.; Schwandner, F. M.

2016-12-01

TANSO-FTS onboard GOSAT and grating spectrometer on OCO-2 use different measurement techniques to measure carbon dioxide (CO2) and molecular oxygen (O2). Both instruments observe sunlight reflected from the Earth's surface in almost the same spectral range. As a first step in cross calibrating these two instruments, we compared spectral radiance observations within the three short wave infrared (SWIR) spectral bands centered on the O2 A-band (O2A), the weak CO2 band near 1.6 microns (Weak-CO2) and 2.06 micons (Strong-CO2) bands at temporally coincident and spatially collocated points. In this work, we reconciled the different size of the footprints and evaluated at various types of surface targets such as ocean, desert and forest. For radiometric inter-comparisons, we consider long term instrument sensitivity degradation in orbit and differences in viewing geometry and associated differences in surface bidirectional reflectance distribution function (BRDF). Measured spectral radiances agree very well within 5% for all bands. This presentation will summarize these comparisons of GOSAT and OCO-2 spectral radiance observations and associated estimates of carbon dioxide and related parameters retrieved with the same algorithm at matchup points. We will also discuss instrument related uncertainties from various target observations.

Statistical downscaling of IPCC sea surface wind and wind energy predictions for U.S. east coastal ocean, Gulf of Mexico and Caribbean Sea

NASA Astrophysics Data System (ADS)

Yao, Zhigang; Xue, Zuo; He, Ruoying; Bao, Xianwen; Song, Jun

2016-08-01

A multivariate statistical downscaling method is developed to produce regional, high-resolution, coastal surface wind fields based on the IPCC global model predictions for the U.S. east coastal ocean, the Gulf of Mexico (GOM), and the Caribbean Sea. The statistical relationship is built upon linear regressions between the empirical orthogonal function (EOF) spaces of a cross- calibrated, multi-platform, multi-instrument ocean surface wind velocity dataset (predictand) and the global NCEP wind reanalysis (predictor) over a 10 year period from 2000 to 2009. The statistical relationship is validated before applications and its effectiveness is confirmed by the good agreement between downscaled wind fields based on the NCEP reanalysis and in-situ surface wind measured at 16 National Data Buoy Center (NDBC) buoys in the U.S. east coastal ocean and the GOM during 1992-1999. The predictand-predictor relationship is applied to IPCC GFDL model output (2.0°×2.5°) of downscaled coastal wind at 0.25°×0.25° resolution. The temporal and spatial variability of future predicted wind speeds and wind energy potential over the study region are further quantified. It is shown that wind speed and power would significantly be reduced in the high CO2 climate scenario offshore of the mid-Atlantic and northeast U.S., with the speed falling to one quarter of its original value.

Stimulated Bacterial Growth under Elevated pCO2: Results from an Off-Shore Mesocosm Study

PubMed Central

Endres, Sonja; Galgani, Luisa; Riebesell, Ulf; Schulz, Kai-Georg; Engel, Anja

2014-01-01

Marine bacteria are the main consumers of freshly produced organic matter. Many enzymatic processes involved in the bacterial digestion of organic compounds were shown to be pH sensitive in previous studies. Due to the continuous rise in atmospheric CO2 concentration, seawater pH is presently decreasing at a rate unprecedented during the last 300 million years but the consequences for microbial physiology, organic matter cycling and marine biogeochemistry are still unresolved. We studied the effects of elevated seawater pCO2 on a natural plankton community during a large-scale mesocosm study in a Norwegian fjord. Nine Kiel Off-Shore Mesocosms for Future Ocean Simulations (KOSMOS) were adjusted to different pCO2 levels ranging initially from ca. 280 to 3000 µatm and sampled every second day for 34 days. The first phytoplankton bloom developed around day 5. On day 14, inorganic nutrients were added to the enclosed, nutrient-poor waters to stimulate a second phytoplankton bloom, which occurred around day 20. Our results indicate that marine bacteria benefit directly and indirectly from decreasing seawater pH. During the first phytoplankton bloom, 5–10% more transparent exopolymer particles were formed in the high pCO2 mesocosms. Simultaneously, the efficiency of the protein-degrading enzyme leucine aminopeptidase increased with decreasing pH resulting in up to three times higher values in the highest pCO2/lowest pH mesocosm compared to the controls. In general, total and cell-specific aminopeptidase activities were elevated under low pH conditions. The combination of enhanced enzymatic hydrolysis of organic matter and increased availability of gel particles as substrate supported up to 28% higher bacterial abundance in the high pCO2 treatments. We conclude that ocean acidification has the potential to stimulate the bacterial community and facilitate the microbial recycling of freshly produced organic matter, thus strengthening the role of the microbial loop in the surface ocean. PMID:24941307

Transcriptomic response of the Antarctic pteropod Limacina helicina antarctica to ocean acidification.

PubMed

Johnson, Kevin M; Hofmann, Gretchen E

2017-10-23

Ocean acidification (OA), a change in ocean chemistry due to the absorption of atmospheric CO 2 into surface oceans, challenges biogenic calcification in many marine organisms. Ocean acidification is expected to rapidly progress in polar seas, with regions of the Southern Ocean expected to experience severe OA within decades. Biologically, the consequences of OA challenge calcification processes and impose an energetic cost. In order to better characterize the response of a polar calcifier to conditions of OA, we assessed differential gene expression in the Antarctic pteropod, Limacina helicina antarctica. Experimental levels of pCO 2 were chosen to create both contemporary pH conditions, and to mimic future pH expected in OA scenarios. Significant changes in the transcriptome were observed when juvenile L. h. antarctica were acclimated for 21 days to low-pH (7.71), mid-pH (7.9) or high-pH (8.13) conditions. Differential gene expression analysis of individuals maintained in the low-pH treatment identified down-regulation of genes involved in cytoskeletal structure, lipid transport, and metabolism. High pH exposure led to increased expression and enrichment for genes involved in shell formation, calcium ion binding, and DNA binding. Significant differential gene expression was observed in four major cellular and physiological processes: shell formation, the cellular stress response, metabolism, and neural function. Across these functional groups, exposure to conditions that mimic ocean acidification led to rapid suppression of gene expression. Results of this study demonstrated that the transcriptome of the juvenile pteropod, L. h. antarctica, was dynamic and changed in response to different levels of pCO 2 . In a global change context, exposure of L. h. antarctica to the low pH, high pCO 2 OA conditions resulted in a suppression of transcripts for genes involved in key physiological processes: calcification, metabolism, and the cellular stress response. The transcriptomic response at both acute and longer-term acclimation time frames indicated that contemporary L. h. antarctica may not have the physiological plasticity necessary for adaptation to OA conditions expected in future decades. Lastly, the differential gene expression results further support the role of shelled pteropods such as L. h. antarctica as sentinel organisms for the impacts of ocean acidification.

A diatom record of CO2 decline since the late Miocene

NASA Astrophysics Data System (ADS)

Mejía, Luz María; Méndez-Vicente, Ana; Abrevaya, Lorena; Lawrence, Kira T.; Ladlow, Caroline; Bolton, Clara; Cacho, Isabel; Stoll, Heather

2017-12-01

Extratropical sea surface temperature records from alkenones record a dramatic cooling of up to 17 °C over the last ∼14 Ma, but the relationship between this cooling and greenhouse gas forcing has been elusive due to sparse and contrasting reconstructions of atmospheric CO2 for the time period. Alkenone carbon isotopic fractionation during photosynthesis has previously been used to estimate changes in pCO2 over this interval, but is complicated by significant changes in cell size of the alkenone-producing coccolithophorids over this time period. In this study, we reconstruct carbon isotopic fractionation during photosynthesis (εp) using organic compounds trapped within the frustules of pennate diatoms in sediments from the Eastern Equatorial Pacific Ocean at Ocean Drilling Program Site 846 over the last ∼13 Ma. Physical separation of pennate diatoms prior to measuring carbon isotopic fractionation enables us to obtain a record with constant cell geometry, eliminating this factor of uncertainty in our pCO2 reconstruction. In the past ∼11 Ma, εp declines from 15.5 to 10.3‰. Using the classic diffusive model and taking into account variations in opal content, alkenone concentration and coccolith Sr/Ca as indicators of past productivity and growth rate, and sea surface temperature records from the site, we estimate a decline in pCO2 from 454 (+ / - 41) to 250 (+ / - 15) ppmv between ∼11 and 6 Ma. Models accounting for changing the significance of active carbon uptake for photosynthesis, which likely produce more accurate CO2 estimates, suggest a significant larger pCO2 decline of up to twice that shown by the classic diffusive model (in average from 794 (+ / - 233) ppmv at ∼11 Ma to 288 (+/-25) ppmv at ∼6 Ma, considering growth rates varying between 0.5 and 1.7 day-1). Large uncertainties in the pCO2 estimated between ∼8 and 11 Ma using the active uptake model are related to the growth rate used for calculations. Together, these results suggest CO2 forcing for this period of steep decline in temperatures.

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

PubMed Central

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

2016-01-01

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 14C 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. PMID:27187527

Ventilation of the deep Southern Ocean and changes in atmospheric CO2 during the last deglacial and glacial periods

NASA Astrophysics Data System (ADS)

Gottschalk, J.; Skinner, L. C.; Lippold, J. A.; Jaccard, S.; Vogel, H.; Frank, N.; Waelbroeck, C.

2014-12-01

The Southern Ocean is thought to have played a key role in atmospheric CO2 (CO2,atm) variations, both via its role in bringing carbon-rich deep-waters into contact with the atmosphere, and via its capacity for enhanced biologically mediated carbon export into the deep sea. The governing mechanisms of millennial scale rises in CO2,atm during the last deglacial and glacial periods have been linked controversially either with variations in biological export productivity, possibly driven by fluctuations in airborne dust supply, or to variations in southern high-latitude vertical mixing, possibly driven by changes in westerly wind stress or density stratification across the Southern Ocean water column. However, the impact of these processes on deep, southern high-latitude carbon sequestration and ocean-atmosphere CO2 exchange remain ambiguous. We present proxy evidence for the link between deep carbon storage in the sub-Antarctic Atlantic with changes in CO2,atm during the last 70 ka from sub-millennially resolved changes in bottom water oxygenation based on the uranium accumulation in authigenic coatings on foraminiferal shells and the δ13C offset between epibenthic and infaunal foraminifera (Δδ13C). We compare our results with reconstructed opal fluxes and sediment model output data to assess the impact of physical and biological processes on Southern Ocean carbon storage. While variations in sub-Antarctic Atlantic export production are intrinsically linked with changes in airborne dust supply supporting the major impact of dust on the biological soft-tissue pump, they cannot account for observed changes in pore water organic carbon respiration indicated by increasing Δδ13C and therefore, bottom water oxygen changes in the deep sub-Antarctic Atlantic. This is in strong support of millennial-scale fluctuations in deep Southern Ocean carbon storage primarily controlled by the ventilation of the deep ocean by southern-sourced water masses, which emphasize the strong control of vertical mixing and upwelling of CO2-rich water masses in the Southern Ocean on the ocean-atmosphere exchange of CO2 and variation in CO2,atm over both glacial-interglacial and millennial time scales.

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

NASA Astrophysics Data System (ADS)

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

2008-12-01

Ocean CO2 storage that actively utilizes the ocean potential to dissolve extremely large amounts of CO2 is a useful option with the intent of diminishing atmospheric CO2 concentration. CO2 storage into sub-seabed geological formations is also considered as the option which has been already put to practical reconnaissance in some projects. Direct release of CO2 in the ocean storage and potential CO2 leakage from geological formations into the bottom water can alter carbonate system as well as pH of seawater. It is essential to examine to what direction and extent chemistry change of seawater induced by CO2 can affect the marine environments. Previous studies have shown direct and acute effects by increasing CO2 concentrations on physiology of marine organisms. It is also a serious concern that chemistry change can affect the rates of chemical, biochemical and microbial processes in seawater resulting in significant influences on marine biogeochemical cycles of the bioelements including carbon, nutrients and trace metals. We, AIST, have conducted a series of basic researches to assess the potential impacts of ocean CO2 storage on marine biogeochemical processes including CaCO3 dissolution, and bacterial and enzymatic decomposition of organic matter. By laboratory experiments using a special high pressure apparatus, the improved empirical equation was obtained for CaCO3 dissolution rate in the high CO2 concentrations. Based on the experimentally obtained kinetics with a numerical simulation for a practical scenario of oceanic CO2 sequestration where 50 Mton CO2 per year is continuously injected to 1,000-2,500 m depth within 100 x 333 km area for 30 years, we could illustrate precise 3-D maps for the predicted distributions of the saturation depth of CaCO3, in situ Ω value and CaCO3 dissolution rate in the western North Pacific. The result showed no significant change in the bathypelagic CaCO3 flux due to chemistry change induced by ocean CO2 sequestration. Both bacteria and hydrolytic enzymes are known as the essential promoters for organic matter decomposition in marine ecosystems. Bacterial activity and metabolisms under various CO2 concentrations and pH were examined on total cell abundance, 3H-leucine incorporation rate, and viable cell abundance. Our in vitro experiments demonstrated that acute effect by high CO2 conditions was negligible on the activities of bathypelagic bacteria at pH 7 or higher. However, our results suggested that bacterial assemblage in some organic-rich "microbial hot-spots" in seawater such as organic aggregates sinking particles, exhibited high sensitivity to acidification. Furthermore, it was indicated that CO2 injection seems to be the trigger to alter the microbial community structure between Eubacteria and Archaea. The activities of five types of hydrolytic enzymes showed no significant change with acidification as those observed in the bacterial activity. As to acute effects on microbial and biochemical processes examined by our laboratory studies, no significant influence was exhibited in the simulated ocean CO2 storage on marine biogeochemical cycling. Uncertainties in chronic and large-scale impacts, however, remain and should be addressed for more understanding the potential benefits and risks of the ocean storage.

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

NASA Astrophysics Data System (ADS)

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

2018-04-01

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

Ocean acidification does not affect the physiology of the tropical coral Acropora digitifera during a 5-week experiment

NASA Astrophysics Data System (ADS)

Takahashi, A.; Kurihara, H.

2013-03-01

The increase in atmospheric CO2 concentration, which has resulted from the burning of fossil fuels, is being absorbed by the oceans and is causing ocean acidification. Ocean acidification involves the decrease of both the pH and the calcium carbonate saturation state. Ocean acidification is predicted to impact the physiology of marine organisms and reduce the calcification rates of corals. In the present study, we measured the rates of calcification, respiration, photosynthesis, and zooxanthellae density of the tropical coral Acropora digitifera under near-natural summertime temperature and sunlight for a 5-week period. We found that these key physiological parameters were not affected by both mid-CO2 (pCO2 = 744 ± 38, pH = 7.97 ± 0.02, Ωarag = 2.6 ± 0.1) and high-CO2 conditions (pCO2 = 2,142 ± 205, pH = 7.56 ± 0.04, Ωarag = 1.1 ± 0.2) throughout the 35 days experimental period. Additionally, there was no significant correlation between calcification rate and seawater aragonite saturation (Ωarag). These results suggest that the impacts of ocean acidification on corals physiology may be more complex than have been previously proposed.

The Coastal Carbonate Chemistry in Bolinao-Anda, Pangasinan, Northern Philippines

NASA Astrophysics Data System (ADS)

Lagumen, M. C. T.; San Diego-McGlone, M. L.; Araujo, M.; Noriega, C.

2016-12-01

The coastal ocean represents only 7% of the total ocean area, but the interactions of CO2 (dissolved, atmospheric) within the coastal area is very dynamic. This study was conducted in the coastal waters of the Bolinao-Anda channel, Pangasinan, Philippines. The 28 stations were divided into 3 groups: coral, seagrass and mariculture area. Samples were collected for carbonate parameters namely total alkalinity (TA), dissolved inorganic carbon (DIC) and pH. Air-sea surface CO2 flux (FCO2) was estimated from the difference between partial pressure of CO2 at sea surface (pCO2) and the concentration of CO2 in the atmosphere (pCO2atm). TA ranged from 1226 to 2240 µmol/kg with highest value in the seagrass stations and lowest in the mariculture stations. Mean TA in coral and seagrass stations were similar at 2104.11 ± 6.54 µmol/kg and 2093.32 ± 62.67 µmol/kg, respectively. DIC ranged from 1270.12 µmol/kg to 2006.26 µmol/kg. Mean DIC values were 1868.12 ± 20.25 µmol/kg for coral stations, 1776.82 ± 87.87 µmol/kg for seagrass stations, and 1715.94 ± 52.61 µmol/kg for mariculture stations. A higher range of pH (7.95 to 8.52) and Ωarg (1.97 to 4.85) were determined for the coral and seagrass stations compared to mariculture stations. Mean pH value in mariculture stations was 7.60 ± 0.04, while the mean pH of coral stations was 8.05 ± 0.03, and seagrass stations was 8.27 ± 0.09. The mariculture area is a source of CO2 with flux of 44.72 mmol m-2 day-1 and the coral area too athough flux is small at 0.31 mmol m-2 day-1, while the seagrass area is a sink for CO2 with mean flux of -5.91 mmol m-2 day-1. It is likely that water quality conditions due to mariculture can affect the corals and seagrass areas due to the hydrodynamics of the area.

Reduced calcification and lack of acclimatization by coral colonies growing in areas of persistent natural acidification

PubMed Central

Crook, Elizabeth D.; Cohen, Anne L.; Rebolledo-Vieyra, Mario; Hernandez, Laura; Paytan, Adina

2013-01-01

As the surface ocean equilibrates with rising atmospheric CO2, the pH of surface seawater is decreasing with potentially negative impacts on coral calcification. A critical question is whether corals will be able to adapt or acclimate to these changes in seawater chemistry. We use high precision CT scanning of skeletal cores of Porites astreoides, an important Caribbean reef-building coral, to show that calcification rates decrease significantly along a natural gradient in pH and aragonite saturation (Ωarag). This decrease is accompanied by an increase in skeletal erosion and predation by boring organisms. The degree of sensitivity to reduced Ωarag measured on our field corals is consistent with that exhibited by the same species in laboratory CO2 manipulation experiments. We conclude that the Porites corals at our field site were not able to acclimatize enough to prevent the impacts of local ocean acidification on their skeletal growth and development, despite spending their entire lifespan in low pH, low Ωarag seawater. PMID:23776217

Simple global carbon model: The atmosphere-terrestrial biosphere-ocean interaction

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kwon, O.Y.; Schnoor, J.L.

A simple global carbon model has been developed for scenario analysis, and research needs prioritization. CO{sub 2} fertilization and temperature effects are included in the terrestrial biosphere compartment, and the ocean compartment includes inorganic chemistry which, with ocean water circulation, enables the calculation of time-variable oceanic carbon uptake. Model-derived Q{sub 10} values (the increasing rate for every 10{degrees}C increase of temperature) are 1.37 for land biota photosynthesis, 1.89 for land biota respiration, and 1.95 for soil respiration, and feedback temperature is set at 0.01{degrees}C/ppm of CO{sub 2}. These could be the important parameters controlling the carbon cycle in potential globalmore » warming scenarios. Scenario analysis, together with sensitivity analysis of temperature feedback, suggests that if CO{sub 2} emissions from fossil fuel combustion continue at the present increasing rate of {approximately}1.5% per year, a CO{sub 2} doubling (to 560 ppm) will appear in year 2060. Global warming would be responsible for 40 Gt as carbon (Gt C) accumulation in the land biota, 88 Gt C depletion from the soil carbon, a 7 Gt C accumulation in the oceans, and a 19 ppm increase in atmospheric CO{sub 2}. The ocean buffering capacity to take up the excess CO{sub 2} will decrease with the increasing atmospheric CO{sub 2} concentration. 51 refs., 8 figs., 3 tabs.« less