ALBERT

Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Global Biogeochemical Cycles 32 (2018): 1476-1497, doi:10.1029/2017GB005855.

Description: It has become clear that anthropogenic carbon invasion into the surface ocean drives changes in the seasonal cycles of carbon dioxide partial pressure (pCO2) and pH. However, it is not yet known whether the resulting sea‐air CO2 fluxes are symmetric in their seasonal expression. Here we consider a novel application of observational constraints and modeling inferences to test the hypothesis that changes in the ocean's Revelle factor facilitate a seasonally asymmetric response in pCO2 and the sea‐air CO2 flux. We use an analytical framework that builds on observed sea surface pCO2 variability for the modern era and incorporates transient dissolved inorganic carbon concentrations from an Earth system model. Our findings reveal asymmetric amplification of pCO2 and pH seasonal cycles by a factor of two (or more) above preindustrial levels under Representative Concentration Pathway 8.5. These changes are significantly larger than observed modes of interannual variability and are relevant to climate feedbacks associated with Revelle factor perturbations. Notably, this response occurs in the absence of changes to the seasonal cycle amplitudes of dissolved inorganic carbon, total alkalinity, salinity, and temperature, indicating that significant alteration of surface pCO2 can occur without modifying the physical or biological ocean state. This result challenges the historical paradigm that if the same amount of carbon and nutrients is entrained and subsequently exported, there is no impact on anthropogenic carbon uptake. Anticipation of seasonal asymmetries in the sea surface pCO2 and CO2 flux response to ocean carbon uptake over the 21st century may have important implications for carbon cycle feedbacks.

Description: Cooperative Institute for Climate Science Grant Number: NA17RJ2612; David and Lucile Packard Foundation/MBARI Grant Number: 4696; NOAA Office of Climate Observations Grant Number: NA11OAR4310066; NOAA. Grant Number NA11OAR4310066; KBR Grant Numbers: A08OAR4320752, NA17RJ2612

Description: Author Posting. © The Authors, 2005. This is the author's version of the work. It is posted here by permission of Nature Publishing Group for personal use, not for redistribution. The definitive version was published in Nature 437 (2005): 681-686, doi:10.1038/nature04095.

Description: The surface ocean is everywhere saturated with respect to calcium carbonate (CaCO3). Yet increasing atmospheric CO2 reduces ocean pH and carbonate ion concentrations [CO32−] and thus the level of saturation. Reduced saturation states are expected to affect marine calcifiers even though it has been estimated that all surface waters will remain saturated for centuries. Here we show, however, that some surface waters will become undersaturated within decades. When atmospheric CO2 reaches 550 ppmv, in year 2050 under the IS92a business-as-usual scenario, Southern Ocean surface waters begin to become undersaturated with respect to aragonite, a metastable form of CaCO3. By 2100 as atmospheric CO2 reaches 788 ppmv, undersaturation extends throughout the entire Southern Ocean (〈 60°S) and into the subarctic Pacific. These changes will threaten high-latitude aragonite secreting organisms including cold-water corals, which provide essential fish habitat, and shelled pteropods, an abundant food source for marine predators.

Description: All but the climate simulations were made as part of the OCMIP project, which was launched in 1995 by the Global Analysis, Interpretation, and Modeling (GAIM) Task Force of the International Geosphere-Biosphere Program (IGBP) with funding from NASA. OCMIP-2 was supported by the EU GOSAC project and the U.S. JGOFS SMP funded through NASA. The interannual simulation was supported by the EU NOCES project, which is part of OCMIP-3.

Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 114 (2009): C12099, doi:10.1029/2009JC005835.

Description: The seasonal cycle is the dominant mode of variability in the air-sea CO2 flux in most regions of the global ocean, yet discrepancies between different seasonality estimates are rather large. As part of the Regional Carbon Cycle Assessment and Processes Phase 2 project (RECCAP2), we synthesize surface ocean pCO2 and air-sea CO2 flux seasonality from models and observation-based estimates, focusing on both a present-day climatology and decadal changes between the 1980s and 2010s. Four main findings emerge: First, global ocean biogeochemistry models (GOBMs) and observation-based estimates (pCO2 products) of surface pCO2 seasonality disagree in amplitude and phase, primarily due to discrepancies in the seasonal variability in surface DIC. Second, the seasonal cycle in pCO2 has increased in amplitude over the last three decades in both pCO2 products and GOBMs. Third, decadal increases in pCO2 seasonal cycle amplitudes in subtropical biomes for both pCO2 products and GOBMs are driven by increasing DIC concentrations stemming from the uptake of anthropogenic CO2 (Cant). In subpolar and Southern Ocean biomes, however, the seasonality change for GOBMs is dominated by Cant invasion, whereas for pCO2 products an indeterminate combination of Cant invasion and climate change modulates the changes. Fourth, biome-aggregated decadal changes in the amplitude of pCO2 seasonal variability are largely detectable against both mapping uncertainty (reducible) and natural variability uncertainty (irreducible), but not at the gridpoint scale over much of the northern subpolar oceans and over the Southern Ocean, underscoring the importance of sustained high-quality seasonally resolved measurements over these regions.

Description: This contribution to the RECCAP2 (REgional Carbon Cycle Assessment and Processes) assessment analyzes the processes that determine the global ocean carbon sink, and its trends and variability over the period 1985–2018, using a combination of models and observation-based products. The mean sea-air CO2 flux from 1985 to 2018 is −1.6 ± 0.2 PgC yr−1 based on an ensemble of reconstructions of the history of sea surface pCO2 (pCO2 products). Models indicate that the dominant component of this flux is the net oceanic uptake of anthropogenic CO2, which is estimated at −2.1 ± 0.3 PgC yr−1 by an ensemble of ocean biogeochemical models, and −2.4 ± 0.1 PgC yr−1 by two ocean circulation inverse models. The ocean also degasses about 0.65 ± 0.3 PgC yr−1 of terrestrially derived CO2, but this process is not fully resolved by any of the models used here. From 2001 to 2018, the pCO2 products reconstruct a trend in the ocean carbon sink of −0.61 ± 0.12 PgC yr−1 decade−1, while biogeochemical models and inverse models diagnose an anthropogenic CO2-driven trend of −0.34 ± 0.06 and −0.41 ± 0.03 PgC yr−1 decade−1, respectively. This implies a climate-forced acceleration of the ocean carbon sink in recent decades, but there are still large uncertainties on the magnitude and cause of this trend. The interannual to decadal variability of the global carbon sink is mainly driven by climate variability, with the climate-driven variability exceeding the CO2-forced variability by 2–3 times. These results suggest that anthropogenic CO2 dominates the ocean CO2 sink, while climate-driven variability is potentially large but highly uncertain and not consistently captured across different methods.

Description: Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Oceans 126(8), (2021): e2021JC017510, https://doi.org/10.1029/2021JC017510.

Description: The air-sea exchange of oxygen (O2) is driven by changes in solubility, biological activity, and circulation. The total air-sea exchange of O2 has been shown to be closely related to the air-sea exchange of heat on seasonal timescales, with the ratio of the seasonal flux of O2 to heat varying with latitude, being higher in the extratropics and lower in the subtropics. This O2/heat ratio is both a fundamental biogeochemical property of air-sea exchange and a convenient metric for testing earth system models. Current estimates of the O2/heat flux ratio rely on sparse observations of dissolved O2, leaving it fairly unconstrained. From a model ensemble we show that the ratio of the seasonal amplitude of two atmospheric tracers, atmospheric potential oxygen (APO) and the argon-to-nitrogen ratio (Ar/O2), exhibits a close relationship to the O2/heat ratio of the extratropics (40–70°). The amplitude ratio, A APO/A ArN2, is relatively constant within the extratropics of each hemisphere due to the zonal mixing of the atmosphere. A APO/A ArN2 is not sensitive to atmospheric transport, as most of the observed spatial variability in the seasonal amplitude of δAPO is compensated by similar variations in δ(Ar/N2). From the relationship between O2/heat and A APO/A ArN2 in the model ensemble, we determine that the atmospheric observations suggest hemispherically distinct O2/heat flux ratios of 3.3 ± 0.3 and 4.7 ± 0.8 nmol J-1 between 40 and 70° in the Northern and Southern Hemispheres respectively, providing a useful constraint for O2 and heat air-sea fluxes in earth system models and observation-based data products.

Description: The recent atmospheric measurements of the Scripps program have been supported via funding from the NSF and the National Oceanographic and Atmospheric Administration (NOAA) under grants 1304270 and OAR-CIPO-2015-2004269. M. Manizza and R. F. Keeling thank NSF for financial support via the OCE-1130976 grant. M. Manizza thanks additional financial support from NSF via the ARRA OCE-0850350 grant. S. C. Doney acknowledges support from NSF PLR-1440435. Keith Rodgers acknowledges support from IBS-R028-D1. Gael Forget and the ECCO group kindly provided the ECCOv4 heat fluxes.

Description: 2022-01-22

Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 114 (2009): C09013, doi:10.1029/2008JC005183.

Description: Here we use observations and ocean models to identify mechanisms driving large seasonal to interannual variations in dissolved inorganic carbon (DIC) and dissolved oxygen (O2) in the upper ocean. We begin with observations linking variations in upper ocean DIC and O2 inventories with changes in the physical state of the ocean. Models are subsequently used to address the extent to which the relationships derived from short-timescale (6 months to 2 years) repeat measurements are representative of variations over larger spatial and temporal scales. The main new result is that convergence and divergence (column stretching) attributed to baroclinic Rossby waves can make a first-order contribution to DIC and O2 variability in the upper ocean. This results in a close correspondence between natural variations in DIC and O2 column inventory variations and sea surface height (SSH) variations over much of the ocean. Oceanic Rossby wave activity is an intrinsic part of the natural variability in the climate system and is elevated even in the absence of significant interannual variability in climate mode indices. The close correspondence between SSH and both DIC and O2 column inventories for many regions suggests that SSH changes (inferred from satellite altimetry) may prove useful in reducing uncertainty in separating natural and anthropogenic DIC signals (using measurements from Climate Variability and Predictability's CO2/Repeat Hydrography program).

Description: This report was prepared by K.B.R. under awards NA17RJ2612 and NA08OAR4320752, which includes support through the NOAA Office of Climate Observations (OCO). The statements, findings, conclusions, and recommendations are those of the authors and do not necessarily reflect the views of the National Oceanic and Atmospheric Administration or the U.S. Department of Commerce. Support for K.B.R. was also provided by the Carbon Mitigation Initiative (CMI) through the support of BP, Amaco, and Ford. R.M.K. was supported by NOAA grants NA17RJ2612, NA08OAR4320752, and NA08OAR4310820. F.F.P. was supported by the European Union FP6 CARBOOCEAN Integrated project (contract 51176), the French OVIDE project, and the Spanish Salvador de Madariaga program (PR2006– 0523). This work was also supported by the European NOCES project (EVK2-CT201-00134). Y.Y. and A.I. are partly supported by CREST, JST of Japan. The long-term OISO observational program in the South Indian Ocean is supported by the following three French institutes: INSU (Institut National des Sciences de l’Univers), IPSL (Institute Pierre-Simon Laplace), and IPEV (Institut Paul-Emile Victor).

Description: © The Author(s), 2014. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 11 (2014): 709-734, doi:10.5194/bg-11-709-2014.

Description: Air–sea CO2 fluxes over the Pacific Ocean are known to be characterized by coherent large-scale structures that reflect not only ocean subduction and upwelling patterns, but also the combined effects of wind-driven gas exchange and biology. On the largest scales, a large net CO2 influx into the extratropics is associated with a robust seasonal cycle, and a large net CO2 efflux from the tropics is associated with substantial interannual variability. In this work, we have synthesized estimates of the net air–sea CO2 flux from a variety of products, drawing upon a variety of approaches in three sub-basins of the Pacific Ocean, i.e., the North Pacific extratropics (18–66° N), the tropical Pacific (18° S–18° N), and the South Pacific extratropics (44.5–18° S). These approaches include those based on the measurements of CO2 partial pressure in surface seawater (pCO2sw), inversions of ocean-interior CO2 data, forward ocean biogeochemistry models embedded in the ocean general circulation models (OBGCMs), a model with assimilation of pCO2sw data, and inversions of atmospheric CO2 measurements. Long-term means, interannual variations and mean seasonal variations of the regionally integrated fluxes were compared in each of the sub-basins over the last two decades, spanning the period from 1990 through 2009. A simple average of the long-term mean fluxes obtained with surface water pCO2 diagnostics and those obtained with ocean-interior CO2 inversions are −0.47 ± 0.13 Pg C yr−1 in the North Pacific extratropics, +0.44 ± 0.14 Pg C yr−1 in the tropical Pacific, and −0.37 ± 0.08 Pg C yr−1 in the South Pacific extratropics, where positive fluxes are into the atmosphere. This suggests that approximately half of the CO2 taken up over the North and South Pacific extratropics is released back to the atmosphere from the tropical Pacific. These estimates of the regional fluxes are also supported by the estimates from OBGCMs after adding the riverine CO2 flux, i.e., −0.49 ± 0.02 Pg C yr−1 in the North Pacific extratropics, +0.41 ± 0.05 Pg C yr−1 in the tropical Pacific, and −0.39 ± 0.11 Pg C yr−1 in the South Pacific extratropics. The estimates from the atmospheric CO2 inversions show large variations amongst different inversion systems, but their median fluxes are consistent with the estimates from climatological pCO2sw data and pCO2sw diagnostics. In the South Pacific extratropics, where CO2 variations in the surface and ocean interior are severely undersampled, the difference in the air–sea CO2 flux estimates between the diagnostic models and ocean-interior CO2 inversions is larger (0.18 Pg C yr−1). The range of estimates from forward OBGCMs is also large (−0.19 to −0.72 Pg C yr−1). Regarding interannual variability of air–sea CO2 fluxes, positive and negative anomalies are evident in the tropical Pacific during the cold and warm events of the El Niño–Southern Oscillation in the estimates from pCO2sw diagnostic models and from OBGCMs. They are consistent in phase with the Southern Oscillation Index, but the peak-to-peak amplitudes tend to be higher in OBGCMs (0.40 ± 0.09 Pg C yr−1) than in the diagnostic models (0.27 ± 0.07 Pg C yr−1).

Description: M. Ishii acknowledges the Meteorological Research Institute’s priority research fund for ocean carbon cycle changes, JSPS Grant-in-Aid for Scientific Research (B) No. 22310017, and MEXT Grant-in-Aid for Scientific Research on Innovative Areas No. 24121003. Support for K. B. Rodgers came under awards NA17RJ2612 and NA08OAR4320752, and support for K. B. Rodgers and R. A. Feely from the NOAA Office of Oceanic and Atmospheric Research (OAR) through the office of Climate Observations (OCO), as well as by funds from NASA’s Research Opportunities in Space and Earth Sciences through award #NNX09AI13G. SMF’s contributions were funded through the NIWA National Centre for Atmosphere’s core research funding. S. C. Doney and I. Lima acknowledge support from US National Science Foundation award AGS-1048827. E. T. Buitenhuis acknowledges support from the EU (CarboChange, contract 264879). A. Lenton acknowledges support from the Australian Climate Change Science Program. T. Takahashi is supported by grants from the NOAA (NA08OAR4320754) and the Comer Science and Education Foundation (CSEF CP70).