Abstract The acidification of coastal waters is distinguished from the open ocean because of much stronger synergistic effects between anthropogenic forcing and local biogeochemical processes. However, ocean acidification research is still rather limited in polar coastal oceans. Here, we present a 17‐year (2002–2019) observational data set in the Chukchi Sea to determine the long‐term changes in pH and aragonite saturation state (Ωarag). We found that pH and Ωaragdeclined in different water masses with average rates of −0.0047 ± 0.0026 years−1and −0.017 ± 0.009 years−1, respectively, and are ∼2–3 times faster than those solely due to increasing atmospheric CO2. We attributed the rapid acidification to the increased dissolved inorganic carbon owing to a combination of ice melt‐induced increased atmospheric CO2invasion and subsurface remineralization induced by a stronger surface biological production as a result of the increased inflow of the nutrient‐rich Pacific water.
more »
« less
A 37-year record of ocean acidification in the Southern California current
Abstract Long-term ocean time series have proven to be the most robust approach for direct observation of climate change processes such as Ocean Acidification. The California Cooperative Oceanic Fisheries Investigations (CalCOFI) program has collected quarterly samples for seawater inorganic carbon since 1983. The longest time series is at CalCOFI line 90 station 90 from 1984–present, with a gap from 2002 to 2008. Here we present the first analysis of this 37- year time series, the oldest in the Pacific. Station 90.90 exhibits an unambiguous acidification signal in agreement with the global surface ocean (decrease in pH of −0.0015 ± 0.0001 yr−1), with a distinct seasonal cycle driven by temperature and total dissolved inorganic carbon. This provides direct evidence that the unique carbon chemistry signature (compared to other long standing time series) results in a reduced uptake rate of carbon dioxide (CO2) due to proximity to a mid-latitude eastern boundary current upwelling zone. Comparison to an independent empirical model estimate and climatology at the same location reveals regional differences not captured in the existing models.
more »
« less
- Award ID(s):
- 2050280
- PAR ID:
- 10472561
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Communications Earth & Environment
- Volume:
- 4
- Issue:
- 1
- ISSN:
- 2662-4435
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract The subpolar North Atlantic plays an outsized role in the atmosphere‐to‐ocean carbon sink. The central Irminger Sea is home to well‐documented deep winter convection and high phytoplankton production, which drive strong seasonal and interannual variability in regional carbon cycling. We use observational data from moored carbonate chemistry system sensors and annual turn‐around cruise samples at the Ocean Observatories Initiative's Irminger Sea Array to construct a near‐continuous time series of mixed layer total dissolved inorganic carbon (DIC),pCO2, and total alkalinity from summer 2015 to summer 2022. We use these carbonate chemistry system time series to deconvolve the physical and biological drivers of surface ocean carbon cycling in this region on seasonal, annual, and interannual time scales. We find high annual net community production within the seasonally varying mixed layer, averaging 9.8 ± 1.6 mol m−2 yr−1with high interannual variability (range of 6.0–13.9 mol m−2 yr−1). The highest daily net community production rates occur during the late winter and early spring, prior to the observed high chlorophyll concentrations associated with the spring phytoplankton bloom. As a result, the winter and early spring play a much larger role in biological carbon export from the mixed layer than traditionally thought.more » « less
-
Abstract In coastal regions and marginal bodies of water, the increase in partial pressure of carbon dioxide (pCO2) in many instances is greater than that of the open ocean due to terrestrial (river, estuarine, and wetland) influences, decreasing buffering capacity and/or increasing water temperatures. Coastal oceans receive freshwater from rivers and groundwater as well as terrestrial-derived organic matter, both of which have a direct influence on coastal carbonate chemistry. The objective of this research is to determine if coastal marshes in Georgia, USA, may be “hot-spots” for acidification due to enhanced inorganic carbon sources and if there is terrestrial influence on offshore acidification in the South Atlantic Bight (SAB). The results of this study show that dissolved inorganic carbon (DIC) and total alkalinity (TA) are elevated in the marshes compared to predictions from conservative mixing of the freshwater and oceanic end-members, with accompanying pH around 7.2 to 7.6 within the marshes and aragonite saturation states (ΩAr) <1. In the marshes, there is a strong relationship between the terrestrial/estuarine-derived organic and inorganic carbon and acidification. Comparisons of pH, TA, and DIC to terrestrial organic material markers, however, show that there is little influence of terrestrial-derived organic matter on shelf acidification during this period in 2014. In addition, ΩArincreases rapidly offshore, especially in drier months (July). River stream flow during 2014 was anomalously low compared to climatological means; therefore, offshore influences from terrestrial carbon could also be decreased. The SAB shelf may not be strongly influenced by terrestrial inputs to acidification during drier than normal periods; conversely, shelf waters that are well-buffered against acidification may not play a significant role in mitigating acidification within the Georgia marshes.more » « less
-
Abstract Ocean acidification due to anthropogenic CO2emission reduces ocean pH and carbonate saturation, with the projection that marine calcifiers and associated ecosystems will be negatively affected in the future. On longer time scale, however, recent studies of deep‐sea carbonate sediments suggest significantly increased carbonate production and burial in the open ocean during the warm Middle Miocene. Here, we present new model simulations in comparison to published Miocene carbonate accumulation rates to show that global biogenic carbonate production in the pelagic environment was approximately doubled relative to present‐day values when elevated atmosphericpCO2led to substantial global warming ∼13–15 million years ago. Our analysis also finds that although high carbonate production was associated with high dissolution in the deep‐sea, net pelagic carbonate burial was approximately 30%–45% higher than modern. At the steady state of the long‐term carbon cycle, this requires an equivalent increase in riverine carbonate alkalinity influx during the Middle Miocene, attributable to enhanced chemical weathering under a warmer climate. Elevated biogenic carbonate production resulted in a Miocene ocean that had carbon (dissolved inorganic carbon) and alkalinity (total alkalinity) inventories similar to modern values but was poorly buffered and less saturated in both the surface and the deep ocean relative to modern.more » « less
-
Abstract Astronomical cycles are strongly expressed in marine geological records, providing important insights into Earth system dynamics and an invaluable means of constructing age models. However, how various astronomical periods are filtered by the Earth system and the mechanisms by which carbon reservoirs and climate components respond, particularly in absence of dynamic ice sheets, is unclear. Using an Earth system model that includes feedbacks between climate, ocean circulation, and inorganic (carbonate) carbon cycling relevant to geological timescales, we systematically explore the impact of astronomically modulated insolation forcing and its expression in model variables most comparable to key paleoceanographic proxies (temperature, the δ13C of inorganic carbon, and sedimentary carbonate content). Temperature predominately responds to short and long eccentricity and is little influenced by the modeled carbon cycle feedbacks. In contrast, the cycling of nutrients and carbon in the ocean generates significant precession power in atmospheric CO2, benthic ocean δ13C, and sedimentary wt% CaCO3, while inclusion of marine sedimentary and weathering processes shifts power to the long eccentricity period. Our simulations produce reducedpCO2and dissolved inorganic carbon (DIC) δ13C at long eccentricity maxima and, contrary to early Cenozoic marine records, CaCO3preservation in the model is enhanced during eccentricity‐modulated warmth. Additionally, the magnitude of δ13C variability simulated in our model underestimates marine proxy records. These model‐data discrepancies hint at the possibility that the Paleogene silicate weathering feedback was weaker than modeled here and that additional organic carbon cycle feedbacks are necessary to explain the full response of the Earth system to astronomical forcing.more » « less
An official website of the United States government
