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Sea-ice melt CO<sub>2</sub>–carbonate chemistry in the western Arctic Ocean: meltwater contributions to air–sea CO<sub>2</sub> gas exchange, mixed-layer properties and rates of net community production under sea ice
oleh: N. R. Bates, R. Garley, K. E. Frey, K. L. Shake, J. T. Mathis
| Format: | Article |
|---|---|
| Diterbitkan: | Copernicus Publications 2014-12-01 |
Deskripsi
The carbon dioxide (CO<sub>2</sub>)-carbonate chemistry of sea-ice melt and co-located, contemporaneous seawater has rarely been studied in sea-ice-covered oceans. Here, we describe the CO<sub>2</sub>–carbonate chemistry of sea-ice melt (both above sea-ice as "melt ponds" and below sea-ice as "interface waters") and mixed-layer properties in the western Arctic Ocean in the early summer of 2010 and 2011. At 19 stations, the salinity (∼0.5 to <6.5), dissolved inorganic carbon (DIC; ∼20 to <550 μmol kg<sup>−1</sup>) and total alkalinity (TA; ∼30 to <500 μmol kg<sup>−1</sup>) of above-ice melt pond water was low compared to the co-located underlying mixed layer. The partial pressure of CO<sub>2</sub> (<i>p</i>CO<sub>2</sub>) in these melt ponds was highly variable (∼<10 to >1500 μatm) with the majority of melt ponds acting as potentially strong sources of CO<sub>2</sub> to the atmosphere. The pH of melt pond waters was also highly variable ranging from mildly acidic (6.1 to 7) to slightly more alkaline than underlying seawater (>8.2 to 10.8). All of the observed melt ponds had very low (<0.1) saturation states (Ω) for calcium carbonate (CaCO<sub>3</sub>) minerals such as aragonite (Ω<sub>aragonite</sub>). Our data suggest that sea-ice generated alkaline or acidic type melt pond water. This melt water chemistry dictates whether the ponds are sources of CO<sub>2</sub> to the atmosphere or CO<sub>2</sub> sinks. Below-ice interface water CO<sub>2</sub>–carbonate chemistry data also indicated substantial generation of alkalinity, presumably owing to dissolution of CaCO<sub>3</sub> in sea-ice. The interface waters generally had lower <i>p</i>CO<sub>2</sub> and higher pH/Ω<sub>aragonite</sub> than the co-located mixed layer beneath. Sea-ice melt thus contributed to the suppression of mixed-layer <i>p</i>CO<sub>2</sub>, thereby enhancing the surface ocean's capacity to uptake CO<sub>2</sub> from the atmosphere. Our observations contribute to growing evidence that sea-ice CO<sub>2</sub>–carbonate chemistry is highly variable and its contribution to the complex factors that influence the balance of CO<sub>2</sub> sinks and sources (and thereby ocean acidification) is difficult to predict in an era of rapid warming and sea-ice loss in the Arctic Ocean.