Ocean Carbon Dioxide Research Articles

Observed changes in ocean acidity and carbon dioxide exchange in the coastal Bay of Bengal – a link to air pollution

Variations in surface water hydrographic properties and dissolved inorganic carbon (DIC) were evaluated in the coastal Bay of Bengal using observations carried out during March–April 1991 and 2011, including 8 yr monthly time-series observations during 2005 and 2013. The coastal Bay of Bengal is characterised by relatively fresher, more basic and lower pCO2 in 1991 compared to 2011. The rates of decrease in pH, increase in DIC and pCO2 per decade were consistent with global trends in the southwestern (SW) coastal Bay of Bengal, whereas rates in the northwestern (NW) coastal Bay of Bengal were observed to be 3–5 times higher. The associated recent increase in sulphate and nitrogen aerosol loadings over NW Bay of Bengal from the Indo-Gangetic Plain and Southeast Asia during winter and spring may be mainly responsible for the increased acidity in recent years. Thus, this region, which was previously considered to be a significant sink for atmospheric CO2, now seems to have become a source of CO2 to the atmosphere.

Temporal changes in surface partial pressure of carbon dioxide and carbonate saturation state in the eastern equatorial Indian Ocean during the 1962–2012 period

Abstract. Information on changes in the oceanic carbon dioxide (CO2) concentration and air–sea CO2 flux as well as on ocean acidification in the Indian Ocean is very limited. In this study, temporal changes of the inorganic carbon system in the eastern equatorial Indian Ocean (EIO, 5° N–5° S, 90–95° E) are examined using partial pressure of carbon dioxide (pCO2) data collected in May 2012, historical pCO2 data since 1962, and total alkalinity (TA) data calculated from salinity. Results show that sea surface pCO2 in the equatorial belt (2° N–2° S, 90–95° E) increased from ∼307 μatm in April 1963 to ∼373 μatm in May 1999, ∼381 μatm in April 2007, and ∼385 μatm in May 2012. The mean rate of pCO2 increase in this area (∼1.56 μatm yr−1) was close to that in the atmosphere (∼1.46 μatm yr−1). Despite the steady pCO2 increase in this region, no significant change in air–sea CO2 fluxes was detected during this period. Ocean acidification as indicated by pH and saturation states for carbonate minerals has indeed taken place in this region. Surface water pH (total hydrogen scale) and saturation state for aragonite (Ωarag), calculated from pCO2 and TA, decreased significantly at rates of −0.0016 ± 0.0001 and −0.0095 ± 0.0005 yr−1, respectively. The respective contributions of temperature, salinity, TA, and dissolved inorganic carbon (DIC) to the increase in surface pCO2 and the decreases in pH and Ωarag are quantified. We find that the increase in DIC dominated these changes, while contributions from temperature, salinity, and TA were insignificant. The increase in DIC was most likely associated with the increasing atmospheric CO2 concentration, and the transport of accumulated anthropogenic CO2 from a CO2 sink region via basin-scale ocean circulations. These two processes may combine to drive oceanic DIC to follow atmospheric CO2 increase.

Uncertainties in measurements of ocean carbon dioxide levels

Carbon dioxide (CO2) emissions are not affecting only the atmosphere: 30% of anthropogenic CO2 emissions were absorbed by the oceans in the past few decades, recent estimates show. However, Kouketsu and Murata note that these estimates are based entirely on research that was conducted in the 1990s and that more recent measurements of oceanic CO2 have not been taken into account.

Responses of calcification of massive and encrusting corals to past, present, and near-future ocean carbon dioxide concentrations

In this study, we report the acidification impact mimicking the pre-industrial, the present, and near-future oceans on calcification of two coral species (Porites australiensis, Isopora palifera) by using precise pCO2 control system which can produce acidified seawater under stable pCO2 values with low variations. In the analyses, we performed Bayesian modeling approaches incorporating the variations of pCO2 and compared the results between our modeling approach and classical statistical one. The results showed highest calcification rates in pre-industrial pCO2 level and gradual decreases of calcification in the near-future ocean acidification level, which suggests that ongoing and near-future ocean acidification would negatively impact coral calcification. In addition, it was expected that the variations of parameters of carbon chemistry may affect the inference of the best model on calcification responses to these parameters between Bayesian modeling approach and classical statistical one even under stable pCO2 values with low variations.

Recent variability of the global ocean carbon sink

AbstractWe present a new observation‐based estimate of the global oceanic carbon dioxide (CO2) sink and its temporal variation on a monthly basis from 1998 through 2011 and at a spatial resolution of 1°×1°. This sink estimate rests upon a neural network‐based mapping of global surface ocean observations of the partial pressure of CO2 (pCO2) from the Surface Ocean CO2 Atlas database. The resulting pCO2 has small biases when evaluated against independent observations in the different ocean basins, but larger randomly distributed differences exist particularly in high latitudes. The seasonal climatology of our neural network‐based product agrees overall well with the Takahashi et al. (2009) climatology, although our product produces a stronger seasonal cycle at high latitudes. From our global pCO2 product, we compute a mean net global ocean (excluding the Arctic Ocean and coastal regions) CO2 uptake flux of −1.42 ± 0.53 Pg C yr−1, which is in good agreement with ocean inversion‐based estimates. Our data indicate a moderate level of interannual variability in the ocean carbon sink (±0.12 Pg C yr−1, 1σ) from 1998 through 2011, mostly originating from the equatorial Pacific Ocean, and associated with the El Niño–Southern Oscillation. Accounting for steady state riverine and Arctic Ocean carbon fluxes our estimate further implies a mean anthropogenic CO2 uptake of −1.99 ± 0.59 Pg C yr−1 over the analysis period. From this estimate plus the most recent estimates for fossil fuel emissions and atmospheric CO2 accumulation, we infer a mean global land sink of −2.82 ± 0.85 Pg C yr−1 over the 1998 through 2011 period with strong interannual variation.

An observing system simulation for Southern Ocean carbon dioxide uptake.

The Southern Ocean is critically important to the oceanic uptake of anthropogenic CO2. Up to half of the excess CO2 currently in the ocean entered through the Southern Ocean. That uptake helps to maintain the global carbon balance and buffers transient climate change from fossil fuel emissions. However, the future evolution of the uptake is uncertain, because our understanding of the dynamics that govern the Southern Ocean CO2 uptake is incomplete. Sparse observations and incomplete model formulations limit our ability to constrain the monthly and annual uptake, interannual variability and long-term trends. Float-based sampling of ocean biogeochemistry provides an opportunity for transforming our understanding of the Southern Ocean CO2 flux. In this work, we review current estimates of the CO2 uptake in the Southern Ocean and projections of its response to climate change. We then show, via an observational system simulation experiment, that float-based sampling provides a significant opportunity for measuring the mean fluxes and monitoring the mean uptake over decadal scales.

Sensitivity of simulated global ocean carbon flux estimates to forcing by reanalysis products

Reanalysis products from MERRA, NCEP2, NCEP1, and ECMWF were used to force an established ocean biogeochemical model to estimate air–sea carbon fluxes (FCO2) and partial pressure of carbon dioxide (pCO2) in the global oceans. Global air–sea carbon fluxes and pCO2 were relatively insensitive to the choice of forcing reanalysis. All global FCO2 estimates from the model forced by the four different reanalyses were within 20% of in situ estimates (MERRA and NCEP1 were within 7%), and all models exhibited statistically significant positive correlations with in situ estimates across the 12 major oceanographic basins. Global pCO2 estimates were within 1% of in situ estimates with ECMWF being the outlier at 0.6%. Basin correlations were similar to FCO2. There were, however, substantial departures among basin estimates from the different reanalysis forcings. The high latitudes and tropics had the largest ranges in estimated fluxes among the reanalyses. Regional pCO2 differences among the reanalysis forcings were muted relative to the FCO2 results. No individual reanalysis was uniformly better or worse in the major oceanographic basins. The results provide information on the characterization of uncertainty in ocean carbon models due to choice of reanalysis forcing.

The Role of the Ocean Carbon Cycle in Climate Change

The ocean carbon cycle plays a twofold role in the context of climate change: (1) through carbon dioxide gas exchange with the atmosphere and carbon cycle climate feedbacks, the ocean regulates the carbon dioxide concentration in the atmosphere and hence has a strong influence on the heat budget of the Earth; (2) the paleo-climatic marine sediment core record is largely based on biogenic matter fluxes from the ocean surface to the sea floor, which are part of the marine carbon cycle. The ocean is important for global carbon cycling, primarily due to three factors: (1) the ocean is a huge carbon reservoir with a relatively short turnover time; (2) carbon dioxide in sea water is effectively dissociated inorganically into other substances; (3) marine plankton is keeping the surface ocean carbon dioxide concentration at a lower level than would a lifeless ocean. On intermediate to long time scales, the ocean provides the most important sink for anthropogenic carbon dioxide. The marine uptake kinetics for carbon dioxide work on a longer time scale than current and projected emissions by humans.

Investigating the complex relationship between in situ Southern Ocean $$pCO_{2}$$ p C O 2 and its ocean physics and biogeochemical drivers using a nonparametric regression approach

The objective in this paper is to investigate the use of a non-parametric approach to model the relationship between oceanic carbon dioxide \((pCO_2)\) and a range of ocean physics and biogeochemical in situ variables in the Southern Ocean, which influence its in situ variability. The need for this stems from the need to obtain reliable estimates of carbon dioxide concentrations in the Southern Ocean which plays an important role in the global carbon flux cycle. The main challenge involved in this objective is the spatial limitation and seasonal bias of the in situ data. Moreover, studies have also reported that the relationship between \(pCO_2\) and its drivers is complex. As such, in this paper, we use the non-parametric kernel regression approach since it is able to accurately capture the complex relationships between the response and predictor variables. In this analysis we use the in situ data obtained from the SANAE49 return leg journey between Antarctic to Cape Town. To the best of our knowledge, this is the first time this data set has been subjected to such analysis. The model variants were developed on a training data subset, and the ‘goodness’ of the models were assessed on an “unseen” test data subset. Results indicate that the nonparametric approach consistently captures the relationship more accurately in terms of mean square error, root mean square error and mean absolute error, over a standard parametric approach (multiple linear regression). These results provide a platform for using the developed nonparametric regression model based on in situ measurements to predict \(pCO_2\) for a larger spatial region in the Southern Ocean based on satellite biogeochemical measurements of predictor variables, given that satellites do not measure \(pCO_2\).

Quantifying and Valuing Potential Climate Change Impacts on Coral Reefs in the United States: Comparison of Two Scenarios

The biological and economic values of coral reefs are highly vulnerable to increasing atmospheric and ocean carbon dioxide concentrations. We applied the COMBO simulation model (COral Mortality and Bleaching Output) to three major U.S. locations for shallow water reefs: South Florida, Puerto Rico, and Hawaii. We compared estimates of future coral cover from 2000 to 2100 for a “business as usual” (BAU) greenhouse gas (GHG) emissions scenario with a GHG mitigation policy scenario involving full international participation in reducing GHG emissions. We also calculated the economic value of changes in coral cover using a benefit transfer approach based on published studies of consumers' recreational values for snorkeling and diving on coral reefs as well as existence values for coral reefs. Our results suggest that a reduced emissions scenario would provide a large benefit to shallow water reefs in Hawaii by delaying or avoiding potential future bleaching events. For Hawaii, reducing emissions is projected to result in an estimated “avoided loss” from 2000 to 2100 of approximately $10.6 billion in recreational use values compared to a BAU scenario. However, reducing emissions is projected to provide only a minor economic benefit in Puerto Rico and South Florida, where sea-surface temperatures are already close to bleaching thresholds and coral cover is projected to drop well below 5% cover under both scenarios by 2050, and below 1% cover under both scenarios by 2100.

Estimating temporal and spatial variation of ocean surface <i>p</i>CO<sub>2</sub> in the North Pacific using a self-organizing map neural network technique

Abstract. 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.

Southern Ocean exports carbon less efficiently than previously thought

The Southern Ocean is a major source of gas exchange between the atmosphere and the ocean, accounting for almost 20% of global ocean carbon dioxide (CO2) uptake. Phytoplankton fix CO2, converting it to other carbon compounds, and some of this biogenic carbon sinks to the deeper ocean, where it is effectively removed from the atmosphere. Better understanding of the rate of export of carbon particulate matter from the upper ocean is key to improving uncertainties in models that include the Southern Ocean's role in the carbon cycle.

A uniform, quality controlled Surface Ocean CO<sub>2</sub> Atlas (SOCAT)

Abstract. A well-documented, publicly available, global data set of surface ocean carbon dioxide (CO2) parameters has been called for by international groups for nearly two decades. The Surface Ocean CO2 Atlas (SOCAT) project was initiated by the international marine carbon science community in 2007 with the aim of providing a comprehensive, publicly available, regularly updated, global data set of marine surface CO2, which had been subject to quality control (QC). Many additional CO2 data, not yet made public via the Carbon Dioxide Information Analysis Center (CDIAC), were retrieved from data originators, public websites and other data centres. All data were put in a uniform format following a strict protocol. Quality control was carried out according to clearly defined criteria. Regional specialists performed the quality control, using state-of-the-art web-based tools, specially developed for accomplishing this global team effort. SOCAT version 1.5 was made public in September 2011 and holds 6.3 million quality controlled surface CO2 data points from the global oceans and coastal seas, spanning four decades (1968–2007). Three types of data products are available: individual cruise files, a merged complete data set and gridded products. With the rapid expansion of marine CO2 data collection and the importance of quantifying net global oceanic CO2 uptake and its changes, sustained data synthesis and data access are priorities.

Surface Ocean CO<sub>2</sub> Atlas (SOCAT) gridded data products

Abstract. As a response to public demand for a well-documented, quality controlled, publically available, global surface ocean carbon dioxide (CO2) data set, the international marine carbon science community developed the Surface Ocean CO2 Atlas (SOCAT). The first SOCAT product is a collection of 6.3 million quality controlled surface CO2 data from the global oceans and coastal seas, spanning four decades (1968–2007). The SOCAT gridded data presented here is the second data product to come from the SOCAT project. Recognizing that some groups may have trouble working with millions of measurements, the SOCAT gridded product was generated to provide a robust, regularly spaced CO2 fugacity (fCO2) product with minimal spatial and temporal interpolation, which should be easier to work with for many applications. Gridded SOCAT is rich with information that has not been fully explored yet (e.g., regional differences in the seasonal cycles), but also contains biases and limitations that the user needs to recognize and address (e.g., local influences on values in some coastal regions).

Phase equilibrium condition of marine carbon dioxide hydrate

The phase equilibrium of ocean carbon dioxide hydrate should be understood for ocean storage of carbon dioxide. In this paper, the isochoric multi-step heating dissociation method was employed to investigate the phase equilibrium of carbon dioxide hydrate in a variety of systems (NaCl solution, submarine pore water, silica sand+NaCl solution mixture). The experimental results show that the depression in the phase equilibrium temperature of carbon dioxide hydrate in NaCl solution is caused mainly by Cl− ion. The relationship between the equilibrium temperature and freezing point in NaCl solution was discussed. The phase equilibrium temperature of carbon dioxide hydrate in submarine pore water is shifted by −1.1K to lower temperature region than that in pure water. However, the phase equilibrium temperature of carbon dioxide hydrate in mixture samples of coarsed-grained silica sand and NaCl solution is in agreement with that in NaCl solution with corresponding concentrations. The relationship between the equilibrium temperature and freezing point in mixture samples was also discussed.

A large increase of the CO2 sink in the western tropical North Atlantic from 2002 to 2009

Determining a robust trend of surface ocean carbon dioxide (CO2) for a period shorter than a decade is challenging due to large seasonal variability and a sparsity of data. Here, we estimate the multiannual trend of surface CO2in the region of 19°N–20°N, 65°W–68°W for the period of 2002–2009. We used an unprecedented number of high‐quality underway data of the fugacity of CO2 in surface seawater (fCO2SW) collected from 137 cruises using an automated system onboard the cruise ship Explorer of the Seas. The growth rate of fCO2SWwas estimated by two de‐seasonalization approaches that showed similar and significantly lower values than the atmospheric increases, leading to a large increase in the CO2 sink. The seasonal difference in the trends was significant, with fCO2SW values in winter showing no increase, while summer fCO2SW values lagged only slightly with the atmosphere. We attribute the lack of an increase in winter fCO2SWvalues to sea surface temperature changes, which are closely correlated with the El Niño‐Southern Oscillation cycle, and to changes in the mixed layer depth. The slower increase of fCO2SWis also related to decreases in salinity. The 8‐year averaged annual net sea‐air CO2 flux was −0.06 ± 0.18 mol m−2 yr−1 compared to a climatology that shows a flux out of the ocean of +0.11 mol m−2 yr−1. The increasing flux differs from previous, mostly longer‐term results for regional studies and time series stations in the North Atlantic, which suggests a decrease or no change in oceanic CO2 uptake.

Late Miocene decoupling of oceanic warmth and atmospheric carbon dioxide forcing

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.

Biosynthesis of Polyhydroxyalkanaotes by a Novel Facultatively Anaerobic Vibrio sp. under Marine Conditions

Marine bacteria have recently attracted attention as potentially useful candidates for the production of practical materials from marine ecosystems, including the oceanic carbon dioxide cycle. The advantages of using marine bacteria for the biosynthesis of poly(hydroxyalkanoate) (PHA), one of the eco-friendly bioplastics, include avoiding contamination with bacteria that lack salt-water resistance, ability to use filtered seawater as a culture medium, and the potential for extracellular production of PHA, all of which would contribute to large-scale industrial production of PHA. A novel marine bacterium, Vibrio sp. strain KN01, was isolated and characterized in PHA productivity using various carbon sources under aerobic and aerobic-anaerobic marine conditions. The PHA contents of all the samples under the aerobic-anaerobic condition, especially when using soybean oil as the sole carbon source, were enhanced by limiting the amount of dissolved oxygen. The PHA accumulated using soybean oil as a sole carbon source under the aerobic-anaerobic condition contained 14% 3-hydroxypropionate (3HP) and 3% 5-hydroxyvalerate (5HV) units in addition to (R)-3-hydroxybutyrate (3HB) units and had a molecular weight of 42 × 10³ g/mol. The present result indicates that the activity of the beta-oxidation pathway under the aerobic-anaerobic condition is reduced due to a reduction in the amount of dissolved oxygen. These findings have potential for use in controlling the biosynthesis of long main-chain PHA by regulating the activity of the beta-oxidation pathway, which also could be regulated by varying the dissolved oxygen concentration.

Convergence of atmospheric and North Atlantic carbon dioxide trends on multidecadal timescales

Oceanic uptake of carbon dioxide reduces the rate at which anthropogenic carbon accumulates in the atmosphere. Trends in oceanic and atmospheric carbon dioxide concentrations converge on a multidecadal timescale, according to an analysis of North Atlantic surface waters.

State of the Climate in 2010

Several large-scale climate patterns influenced climate conditions and weather patterns across the globe during 2010. The transition from a warm El Niño phase at the beginning of the year to a cool La Niña phase by July contributed to many notable events, ranging from record wetness across much of Australia to historically low Eastern Pacific basin and near-record high North Atlantic basin hurricane activity. The remaining five main hurricane basins experienced below- to well-below-normal tropical cyclone activity. The negative phase of the Arctic Oscillation was a major driver of Northern Hemisphere temperature patterns during 2009/10 winter and again in late 2010. It contributed to record snowfall and unusually low temperatures over much of northern Eurasia and parts of the United States, while bringing above-normal temperatures to the high northern latitudes. The February Arctic Oscillation Index value was the most negative since records began in 1950. The 2010 average global land and ocean surface temperature was among the two warmest years on record. The Arctic continued to warm at about twice the rate of lower latitudes. The eastern and tropical Pacific Ocean cooled about 1°C from 2009 to 2010, reflecting the transition from the 2009/10 El Niño to the 2010/11 La Niña. Ocean heat fluxes contributed to warm sea surface temperature anomalies in the North Atlantic and the tropical Indian and western Pacific Oceans. Global integrals of upper ocean heat content for the past several years have reached values consistently higher than for all prior times in the record, demonstrating the dominant role of the ocean in the Earth's energy budget. Deep and abyssal waters of Antarctic origin have also trended warmer on average since the early 1990s. Lower tropospheric temperatures typically lag ENSO surface fluctuations by two to four months, thus the 2010 temperature was dominated by the warm phase El Niño conditions that occurred during the latter half of 2009 and early 2010 and was second warmest on record. The stratosphere continued to be anomalously cool. Annual global precipitation over land areas was about five percent above normal. Precipitation over the ocean was drier than normal after a wet year in 2009. Overall, saltier (higher evaporation) regions of the ocean surface continue to be anomalously salty, and fresher (higher precipitation) regions continue to be anomalously fresh. This salinity pattern, which has held since at least 2004, suggests an increase in the hydrological cycle. Sea ice conditions in the Arctic were significantly different than those in the Antarctic during the year. The annual minimum ice extent in the Arctic—reached in September—was the third lowest on record since 1979. In the Antarctic, zonally averaged sea ice extent reached an all-time record maximum from mid-June through late August and again from mid-November through early December. Corresponding record positive Southern Hemisphere Annular Mode Indices influenced the Antarctic sea ice extents. Greenland glaciers lost more mass than any other year in the decade-long record. The Greenland Ice Sheet lost a record amount of mass, as the melt rate was the highest since at least 1958, and the area and duration of the melting was greater than any year since at least 1978. High summer air temperatures and a longer melt season also caused a continued increase in the rate of ice mass loss from small glaciers and ice caps in the Canadian Arctic. Coastal sites in Alaska show continuous permafrost warming and sites in Alaska, Canada, and Russia indicate more significant warming in relatively cold permafrost than in warm permafrost in the same geographical area. With regional differences, permafrost temperatures are now up to 2°C warmer than they were 20 to 30 years ago. Preliminary data indicate there is a high probability that 2010 will be the 20th consecutive year that alpine glaciers have lost mass. Atmospheric greenhouse gas concentrations continued to rise and ozone depleting substances continued to decrease. Carbon dioxide increased by 2.60 ppm in 2010, a rate above both the 2009 and the 1980–2010 average rates. The global ocean carbon dioxide uptake for the 2009 transition period from La Niña to El Niño conditions, the most recent period for which analyzed data are available, is estimated to be similar to the long-term average. The 2010 Antarctic ozone hole was among the lowest 20% compared with other years since 1990, a result of warmer-than-average temperatures in the Antarctic stratosphere during austral winter between mid-July and early September.