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The ocean holds vast quantities of carbon that it continually exchanges with the atmosphere through the air-sea interface. Because of its enormous size and relatively rapid exchange of carbon with the atmosphere, the ocean controls atmospheric CO 2 concentration and thereby Earth's climate on timescales of tens to thousands of years. This review examines the basic functions of the ocean's carbon cycle, demonstrating that the ocean carbon inventory is determined primarily by the mass of the ocean, by the chemical speciation of CO 2 in seawater, and by the action of the solubility and biological pumps that draw carbon into the ocean's deeper layers, where it can be sequestered for decades to millennia. The ocean also plays a critical role in moderating the impacts of climate change by absorbing an amount of carbon equivalent to about 25% of anthropogenic CO 2 emissions over the past several decades. However, this also leads to ocean acidification and reduces the chemical buffering capacity of the ocean and its future ability to take up CO 2 . This review closes with a look at the uncertain future of the ocean carbon cycle and the scientific challenges that this uncertainty brings. 

Barystatic sea level rise (SLR) caused by the addition of freshwater to the ocean from melting ice can in principle be recorded by a reduction in seawater salinity, but detection of this signal has been hindered by sparse data coverage and the small trends compared to natural variability. Here, we develop an autoregressive machine learning method to estimate salinity changes in the global ocean from 2001 to 2019 that reduces uncertainties in ocean freshening trends by a factor of four compared to previous estimates. We find that the ocean mass rose by 13,000 ± 3,000 Gt from 2001 to 2019, implying a barystatic SLR of 2.0 ± 0.5 mm/yr. Combined with SLR of 1.3 ± 0.1 mm/yr due to ocean thermal expansion, these results suggest that global mean sea level rose by 3.4 ± 0.6 mm/yr from 2001 to 2019. These results provide an important validation of remote‐sensing measurements of ocean mass changes, global SLR, and global ice budgets.

 

Abstract Mid-depth North Pacific waters are rich in nutrients and respired carbon accumulated over centuries. The rates and pathways with which these waters exchange with the surface ocean are uncertain, with divergent paradigms of the Pacific overturning: one envisions bottom waters upwelling to 1.5 km depth; the other confines overturning beneath a mid-depth Pacific shadow zone (PSZ) shielded from mean advection. Here global inverse modelling reveals a PSZ where mean ages exceed 1400 years with overturning beneath. The PSZ is supplied primarily by Antarctic and North-Atlantic ventilated waters diffusing from below and from the south. Half of PSZ waters re-surface in the Southern Ocean, a quarter in the subarctic Pacific. The abyssal North Pacific, despite strong overturning, has mean re-surfacing times also exceeding 1400 years because of diffusion into the overlying PSZ. These results imply that diffusive transports – distinct from overturning transports – are a leading control on Pacific nutrient and carbon storage. 

Abstract. This study considersyear-to-year and decadal variations in as well as secular trendsof the sea–air CO2 flux over the 1957–2020 period,as constrained by the pCO2 measurements from the SOCATv2021 database.In a first step,we relate interannual anomalies in ocean-internal carbon sources and sinksto local interannual anomalies insea surface temperature (SST), the temporal changes in SST (dSST/dt),and squared wind speed (u2),employing a multi-linear regression.In the tropical Pacific, we find interannual variability to be dominated by dSST/dt,as arising from variations in the upwelling of colder and more carbon-rich waters into the mixed layer.In the eastern upwelling zones as well as in circumpolar bands in the high latitudes of both hemispheres,we find sensitivity to wind speed,compatible with the entrainment of carbon-rich water during wind-driven deepening of the mixed layerand wind-driven upwelling.In the Southern Ocean,the secular increase in wind speed leads to a secular increase in the carbon source into the mixed layer,with an estimated reduction in the sink trend in the range of 17 % to 42 %.In a second step,we combined the result of the multi-linear regression andan explicitly interannual pCO2-based additive correctioninto a “hybrid” estimate of the sea–air CO2 flux over the period 1957–2020.As a pCO2 mapping method,it combines (a) the ability of a regression to bridge data gaps and extrapolate intothe early decades almost void of pCO2 databased on process-related observablesand (b) the ability of an auto-regressive interpolation to follow signalseven if not represented in the chosen set of explanatory variables.The “hybrid” estimate can be applied as an ocean flux prior foratmospheric CO2 inversions covering the whole period of atmospheric CO2 data since 1957. 

The ocean is one of the most important sinks for anthropogenic CO₂emissions. Here, I use an ocean circulation inverse model (OCIM), ocean biogeochemical models, and pCO₂interpolation products to examine trends and variability in the oceanic CO₂sink. The OCIM quantifies the impacts of rising atmospheric CO₂, changing sea surface temperatures, and gas transfer velocities on the oceanic CO₂sink. Together, these effects account for an oceanic CO₂uptake of 2.2 ± 0.1 PgC yr⁻¹from 1994 to 2007, and a net increase in the oceanic carbon inventory of 185 PgC from 1780 to 2020. However, these effects cannot account for the majority of the decadal variability shown in data‐based reconstructions of the ocean CO₂sink over the past 30 years. This implies that decadal variability of the ocean CO₂sink is predominantly driven by changes in ocean circulation or biology that act to redistribute both natural and anthropogenic carbon in the ocean.

 

Two centuries of anthropogenic CO₂emissions have increased the CO₂concentration of the atmosphere and the dissolved inorganic carbon (DIC) concentration of the ocean compared to preindustrial times. These anthropogenic carbon perturbations are often equated to the amount of anthropogenically emitted carbon in the atmosphere or ocean, which ignores the possibility of a shift of natural carbon between the oceanic and atmospheric carbon reservoirs. Here we use a data‐assimilated ocean circulation model and numerical tracers akin to ideal isotopes to label carbon when it is emitted by anthropogenic sources. We find that emitted carbon accounts for only about 45% of the atmospheric CO₂increase since preindustrial times, the remaining 55% being natural CO₂that outgassed from the ocean in response to anthropogenically emitted carbon invading the ocean. This outgassing is driven by the order‐10 seawater carbonate buffer factor which causes increased leakage of natural CO₂as DIC concentrations increase. By 2020, the ocean had outgassed ∼159 Pg of natural carbon, which is counteracted by the ocean absorbing ∼347 Pg of emitted carbon, about 1.8 times more than the net increase in oceanic carbon storage of ∼188 PgC. These results do not challenge existing estimates of anthropogenically driven changes in atmospheric or oceanic carbon inventories, but they shed new light on the composition of these changes and the fate of anthropogenically emitted carbon in the Earth system.