No abstract

It has been predicted that the Arctic Ocean will sequester much greater amounts of carbon dioxide (CO2) from the atmosphere as a result of sea ice melt and increasing primary productivity. However, this prediction was made on the basis of observations from either highly productive ocean margins or ice-covered basins before the recent major ice retreat. We report here a high-resolution survey of sea-surface CO2 concentration across the Canada Basin, showing a great increase relative to earlier observations. Rapid CO2 invasion from the atmosphere and low biological CO2 drawdown are the main causes for the higher CO2, which also acts as a barrier to further CO2 invasion. Contrary to the current view, we predict that the Arctic Ocean basin will not become a large atmospheric CO2 sink under ice-free conditions.

Rising atmospheric CO2 concentrations threaten coral reefs globally by causing ocean acidification (OA) and warming. Yet, the combined effects of elevated pCO2 and temperature on coral physiology and resilience remain poorly understood. While coral calcification and energy reserves are important health indicators, no studies to date have measured energy reserve pools (i.e., lipid, protein, and carbohydrate) together with calcification under OA conditions under different temperature scenarios. Four coral species, Acropora millepora, Montipora monasteriata, Pocillopora damicornis, Turbinaria reniformis, were reared under a total of six conditions for 3.5 weeks, representing three pCO2 levels (382, 607, 741 µatm), and two temperature regimes (26.5, 29.0°C) within each pCO2 level. After one month under experimental conditions, only A. millepora decreased calcification (−53%) in response to seawater pCO2 expected by the end of this century, whereas the other three species maintained calcification rates even when both pCO2 and temperature were elevated. Coral energy reserves showed mixed responses to elevated pCO2 and temperature, and were either unaffected or displayed nonlinear responses with both the lowest and highest concentrations often observed at the mid-pCO2 level of 607 µatm. Biweekly feeding may have helped corals maintain calcification rates and energy reserves under these conditions. Temperature often modulated the response of many aspects of coral physiology to OA, and both mitigated and worsened pCO2 effects. This demonstrates for the first time that coral energy reserves are generally not metabolized to sustain calcification under OA, which has important implications for coral health and bleaching resilience in a high-CO2 world. Overall, these findings suggest that some corals could be more resistant to simultaneously warming and acidifying oceans than previously expected.

Total alkalinity (TA) distribution and its relationship with salinity (S) along the western North Atlantic Ocean (wNAO) margins from the Labrador Sea to tropical areas are examined in this study. Based on the observed TA‐S patterns, the mixing processes that control alkalinity distribution in these areas can be categorized into a spectrum of patterns that are bracketed by two extreme mixing types, i.e., alongshore current‐dominated and river‐dominated. Alongshore current‐dominated mixing processes exhibit a segmented mixing line with a shared mid‐salinity end‐member. In such cases (i.e., Labrador Sea, Gulf of Maine, etc.), the y‐intercept of the high salinity segment of the mixing line is generally higher than the local river alkalinity values, and it reflects the mixing history of the alongshore current. In contrast, in river‐dominated mixing (Amazon River, Caribbean Sea, etc.), good linear relationships between alkalinity and salinity are generally observed, and the zero salinity intercepts of the TA‐S regressions roughly match those of the regional river alkalinity values. TA‐S mixing lines can be complicated by rapid changes in the river end‐member value and by another river nearby with a different TA value (e.g., Mississippi‐Atchafalaya/Gulf of Mexico). In the wNAO margins, regression intercepts and river end‐members have a clear latitudinal distribution pattern, increasing from a low of ∼300 μmol kg−1 in the Amazon River plume to a high value between ∼500–1100 μmol kg−1 in the middle and high latitude margins. The highest value of ∼2400 μmol kg−1 is observed in the Mississippi River influenced areas. In addition to mixing control, biological processes such as calcification and benthic alkalinity production may also affect ocean margin alkalinity distribution. Therefore, deriving inorganic carbon system information in coastal oceans using alkalinity‐salinity relationships, in particular, those of generic nature, may lead to significant errors.

Distributions of total alkalinity (TA), dissolved inorganic carbon (DIC), and other parameters relevant to the marine inorganic carbon system were investigated in shelf and adjacent ocean waters during a U.S. Gulf of Mexico and East Coast Carbon cruise in July-August 2007. TA exhibited near-conservative behavior with respect to salinity. Shelf concentrations were generally high in southern waters (Gulf of Mexico and East Florida) and decreased northward from Georgia to the Gulf of Maine. DIC was less variable geographically and exhibited strongly nonconservative behavior. As a result, the ratio of TA to DIC generally decreased northward. The spatial patterns of other CO 2 system parameters closely followed those of the TA : DIC ratio. All sampled shelf waters were supersaturated with respect to aragonite (saturation state V A . 1). The most intensely buffered and supersaturated waters (V A . 5.0) were in northern Gulf of Mexico river-plume waters; the least intensely buffered and least supersaturated waters (V A , 1.3) were in the deep Gulf of Maine. Due to their relatively low pH, V A , and buffer intensity, waters of the northeastern U.S. shelves may be more susceptible to acidification pressures than are their southern counterparts. In the Mid-Atlantic Bight, alongshore mixing tended to increase DIC concentrations southward, but this effect was largely offset by the opposing effects of biogeochemical processing. In the Gulf of Mexico, downstream increases in Loop Current DIC suggested significant contributions from shelf and gulf waters, estimated at 9.1 3 10 9 mol C d 21 . Off the southeastern U.S., along-flow chemical changes in the Florida Current were dominated by mixing associated with North Atlantic subtropical recirculation.

No abstract

Carbon cycling in the coastal zone affects global carbon budgets and is critical for understanding the urgent issues of hypoxia, acidification, and tidal wetland loss. However, there are no regional carbon budgets spanning the three main ecosystems in coastal waters: tidal wetlands, estuaries, and shelf waters. Here we construct such a budget for eastern North America using historical data, empirical models, remote sensing algorithms, and process‐based models. Considering the net fluxes of total carbon at the domain boundaries, 59 ± 12% (± 2 standard errors) of the carbon entering is from rivers and 41 ± 12% is from the atmosphere, while 80 ± 9% of the carbon leaving is exported to the open ocean and 20 ± 9% is buried. Net lateral carbon transfers between the three main ecosystem types are comparable to fluxes at the domain boundaries. Each ecosystem type contributes substantially to exchange with the atmosphere, with CO2 uptake split evenly between tidal wetlands and shelf waters, and estuarine CO2 outgassing offsetting half of the uptake. Similarly, burial is about equal in tidal wetlands and shelf waters, while estuaries play a smaller but still substantial role. The importance of tidal wetlands and estuaries in the overall budget is remarkable given that they, respectively, make up only 2.4 and 8.9% of the study domain area. This study shows that coastal carbon budgets should explicitly include tidal wetlands, estuaries, shelf waters, and the linkages between them; ignoring any of them may produce a biased picture of coastal carbon cycling.

Reliably predicting how coral calcification may respond to ocean acidification and warming depends on our understanding of coral calcification mechanisms. However, the concentration and speciation of dissolved inorganic carbon (DIC) inside corals remain unclear, as only pH has been measured while a necessary second parameter to constrain carbonate chemistry has been missing. Here we report the first carbonate ion concentration ([CO32−]) measurements together with pH inside corals during the light period. We observe sharp increases in [CO32−] and pH from the gastric cavity to the calcifying fluid, confirming the existence of a proton (H+) pumping mechanism. We also show that corals can achieve a high aragonite saturation state (Ωarag) in the calcifying fluid by elevating pH while at the same time keeping [DIC] low. Such a mechanism may require less H+-pumping and energy for upregulating pH compared with the high [DIC] scenario and thus may allow corals to be more resistant to climate change related stressors.