The Arctic Ocean has been recognized to play an active role in global carbon cycle due to its potential to disproportionally take up CO2 from the atmosphere especially under a dwindling ice extent. It is estimated that the Arctic Ocean will be responsible for up to 5%–14% of the total global oceanic CO2 uptake even though it comprises only 3% of the world ocean surface area. Over the past decade, the sea ice in the Arctic Ocean has significantly retreated during summer. The rapid sea ice retreat is thought to cause corresponding changes in the distribution of p CO2 in the surface waters of Arctic Ocean. However, the response of carbon dynamics to a changing Arctic Ocean remains poorly quantified. It has been postulated that an ice-free condition in the Arctic Ocean basins would allow for uptake of a substantial amount of carbon dioxide (CO2) from the atmosphere as a result of sea ice melt and increasing primary productivity. However, the other direct observation-based study of high-resolution survey of sea-surface CO2 concentration across the Canada Basin, showing a great high p CO2 relative to earlier observations and predicted that the Arctic Ocean basin will not become a large atmospheric CO2 sink under ice-free conditions. Due to the existing quite different views, thus, there is an implication of observation-based learning in the variations of the surface seawater p CO2 under a scenario of rapid sea ice melting. In the summer of 2008, during the 3rd Chinese National Arctic Research Expedition (CHINARE) cruise, significant variability of p CO2 in surface water has been observed along a trans-Arctic section of 150°–160°W from the Chukchi Sea slope to 88°N in the western Arctic Ocean. We propose a hypothesis of “low-low-high” variation trend in surface water p CO2 levels along a decreasing ice-cover gradient across three different zones in the Arctic Ocean under a rapid sea ice melting scenario in the summer. Specifically, there are (1) “low” p CO2 levels of ~270–280 μ atm in the sea ice-covered zone (north of 84°N) with a high ice concentration >70%; (2) “low” p CO2 of ~250–270 μ atm in a sea ice melting zone (78°–81°N) with a medium ice extent of around 50%; and (3) “high” p CO2 of ~320–365 μ atm in an ice-free zone (72°–77°N) with a low ice concentration of p CO2 variation trend could be attributed to different driving forces. The low p CO2 in the heavily ice-covered northern basin is likely influenced by a combination of several processes, including mixing of various source waters, CO2 fixation by ice algae, ice-water gas exchange, and temperature change, although their relative roles remain to be quantified. The low p CO2 observed in the partially ice-covered northern Canada Basin could be primarily derived from biological CO2 fixation and the dissolution of CaCO3 precipitates, both of which consume CO2. Primary productivity enhanced by the early melting of sea ice plays an important role in the decreased sea-surface p CO2. In addition, sea ice melting also promotes the dissolution of authigenic CaCO3 in the form of ikaite within the sea ice. Finally, results of tracer data and model simulations suggest that the rapid CO2 invasion from the atmosphere and low biological export of CO2 owing to a shallow mixed-layer depth, strong subsurface water stratification, and limited nutrient supply to the surface water are both responsible for the observed high p CO2 values in the ice-free southern Canada Basin.
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