Abstract Increased oceanic uptake of CO2due to rising anthropogenic emissions has caused lowered pH levels (ocean acidification) that are hypothesized to diminish biotic calcification and reduce the export of total alkalinity (AT) as carbonate minerals from the surface ocean or their burial in coastal sediments. This “CO2‐biotic calcification feedback” is a negative feedback on atmospheric CO2, as elevated levels of surfaceATincrease the ocean's capacity to uptake CO2. We detect signatures of this feedback in the global ocean for the first time using repeat hydrographic measurements and seawater property prediction algorithms. Over the course of the past 30 years, we find an increase in global surfaceATof 0.072 ± 0.023 μmol kg−1 yr−1, which would have caused approximately 20 Tmol of additionalATto accumulate in the surface ocean. This finding suggests that anthropogenic CO2emissions are measurably perturbing the cycling of carbon on a planetary scale by disrupting biological patterns. More observations ofATwould be required to understand the effects of this feedback on a regional basis and to fully characterize its potential to reduce the efficiency of marine carbon dioxide removal technology.
more »
« less
Delayed onset of ocean acidification in the Gulf of Maine
Abstract The Gulf of Maine holds significant ecological and economic value for fisheries and communities in north-eastern North America. However, there is apprehension regarding its vulnerability to the effects of increasing atmospheric CO2. Substantial recent warming and the inflow of low alkalinity waters into the Gulf of Maine have raised concerns about the impact of ocean acidification on resident marine calcifiers (e.g. oysters, clams, mussels). With limited seawater pH records, the natural variability and drivers of pH in this region remain unclear. To address this, we present coastal water pH proxy records using boron isotope (δ11B) measurements in long-lived, annually banded, crustose coralline algae (1920–2018 CE). These records indicate seawater pH was low (~ 7.9) for much of the last century. Contrary to expectation, we also find that pH has increased (+ 0.2 pH units) over the past 40 years, despite concurrent rising atmospheric CO2. This increase is attributed to an increased input of high alkalinity waters derived from the Gulf Stream. This delayed onset of ocean acidification is cause for concern. Once ocean circulation-driven buffering effects reach their limit, seawater pH decline may occur swiftly. This would profoundly harm shellfisheries and the broader Gulf of Maine ecosystem.
more »
« less
- PAR ID:
- 10567794
- Publisher / Repository:
- Scientific Reports
- Date Published:
- Journal Name:
- Scientific Reports
- Volume:
- 15
- Issue:
- 1
- ISSN:
- 2045-2322
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract The ocean carbon reservoir controls atmospheric carbon dioxide (CO2) on millennial timescales. Radiocarbon (14C) anomalies in eastern North Pacific sediments suggest a significant release of geologic14C‐free carbon at the end of the last ice age but without evidence of ocean acidification. Using inverse carbon cycle modeling optimized with reconstructed atmospheric CO2and14C/C, we develop first‐order constraints on geologic carbon and alkalinity release over the last 17.5 thousand years. We construct scenarios allowing the release of 850–2,400 Pg C, with a maximum release rate of 1.3 Pg C yr−1, all of which require an approximate equimolar alkalinity release. These neutralized carbon addition scenarios have minimal impacts on the simulated marine carbon cycle and atmospheric CO2, thereby demonstrating safe and effective ocean carbon storage. This deglacial phenomenon could serve as a natural analog to the successful implementation of gigaton‐scale ocean alkalinity enhancement, a promising marine carbon dioxide removal method.more » « less
-
Abstract The temperature range of Earth's open‐ocean waters is roughly 0–30°C, yet our understanding of the seawater carbon dioxide (CO2) system is largely derived from analyses conducted within a narrow temperature range (e.g., laboratory temperature of 20°C or 25°C). Herein, we address two aspects of open‐ocean CO2‐system measurements and modeling: (1) a highly precise spectrophotometric technique is used to determine bicarbonate dissociation constants (K2) in seawater at temperatures as low as 3°C and (2) a cruise dataset uniquely including total scale pH measurements at two temperatures is used for CO2‐system internal consistency comparisons at 12°C and 25°C. Our pK2parameterization (where pK = −logK) is applicable for broad ranges of salinity (20 ≤ SP ≤ 40) and temperature (3°C ≤ t ≤ 35°C). Our CO2‐system internal consistency evaluation (comparison of measured and calculated CO2‐system parameters) utilized data obtained during NOAA's 2021 West Coast Ocean Acidification Cruise: total alkalinity (TA), total dissolved inorganic carbon (DIC), pH measured at 25°C, and pH measured at 12°C (n = 265). Results demonstrate that, relative to calculations utilizing the TA, DIC pair, agreement between measured and calculated parameters is improved when either TA or DIC is paired with pH measurements at either temperature. Calculations of CO2fugacity (fCO2) and aragonite saturation state (Ωar) using pH measurements made at 25°C or 12°C (paired with either TA or DIC) are statistically indistinguishable. Results also suggest that the temperature dependence of current CO2‐system dissociation constants need further refinement.more » « less
-
Abstract The capacity of aquatic systems to buffer acidification depends on the sum contributions of various chemical species to total alkalinity (TA). Major TA contributors are inorganic, with carbonate and bicarbonate considered the most important. However, growing evidence shows that many rivers, estuaries, and coastal waters contain dissolved organic molecules with charge sites that create organic alkalinity (OrgAlk). This study describes the first comparison of (1) OrgAlk distributions and (2) acid–base properties in contrasting estuary‐plume systems: the Pleasant (Maine, USA) and the St. John (New Brunswick, CA). The substantial concentrations of OrgAlk in each estuary were sometimes not conservative with salinity and typically associated with very low pH. Two approaches to OrgAlk measurement showed consistent differences, indicating acid–base characteristics inconsistent with the TA definition. The OrgAlk fraction of TA ranged from 78% at low salinity to less than 0.4% in the coastal ocean endmember. Modeling of titration data identified three groups of organic charge sites, with mean acid–base dissociation constants (pKa) of 4.2 (± 0.5), 5.9 (± 0.7) and 8.5 (± 0.2). These represented 21% (± 9%), 8% (± 5%), and 71% (± 11%) of titrated organic charge groups. Including OrgAlk, pKa, and titrated organic charge groups in carbonate system calculations improved estimates of pH. However, low and medium salinity, organic‐rich samples demonstrated persistent offsets in calculated pH, even using dissolved inorganic carbon and CO2partial pressure as inputs. These offsets show the ongoing challenge of carbonate system intercomparisons in organic rich systems whereby new techniques and further investigations are needed to fully account for OrgAlk in TA titrations.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
An official website of the United States government

