scholarly journals East–west differences in water mass, nutrient, and chlorophylladistributions in the sea ice reduction region of the western Arctic Ocean

Author(s):  
Shigeto Nishino ◽  
Koji Shimada ◽  
Motoyo Itoh ◽  
Michiyo Yamamoto-Kawai ◽  
Sanae Chiba
2014 ◽  
Vol 11 (7) ◽  
pp. 1705-1716 ◽  
Author(s):  
A. Fujiwara ◽  
T. Hirawake ◽  
K. Suzuki ◽  
I. Imai ◽  
S.-I. Saitoh

Abstract. This study assesses the response of phytoplankton assemblages to recent climate change, especially with regard to the shrinking of sea ice in the northern Chukchi Sea of the western Arctic Ocean. Distribution patterns of phytoplankton groups in the late summers of 2008–2010 were analysed based on HPLC pigment signatures and, the following four major algal groups were inferred via multiple regression and cluster analyses: prasinophytes, diatoms, haptophytes and dinoflagellates. A remarkable interannual difference in the distribution pattern of the groups was found in the northern basin area. Haptophytes dominated and dispersed widely in warm surface waters in 2008, whereas prasinophytes dominated in cold water in 2009 and 2010. A difference in the onset date of sea ice retreat was evident among years–the sea ice retreat in 2008 was 1–2 months earlier than in 2009 and 2010. The spatial distribution of early sea ice retreat matched the areas in which a shift in algal community composition was observed. Steel-Dwass's multiple comparison tests were used to assess the physical, chemical and biological parameters of the four clusters. We found a statistically significant difference in temperature between the haptophyte-dominated cluster and the other clusters, suggesting that the change in the phytoplankton communities was related to the earlier sea ice retreat in 2008 and the corollary increase in sea surface temperatures. Longer periods of open water during the summer, which are expected in the future, may affect food webs and biogeochemical cycles in the western Arctic due to shifts in phytoplankton community structure.


Polar Science ◽  
2020 ◽  
Vol 23 ◽  
pp. 100504
Author(s):  
Di Qi ◽  
Baoshan Chen ◽  
Liqi Chen ◽  
Hongmei Lin ◽  
Zhongyong Gao ◽  
...  

2001 ◽  
Vol 28 (14) ◽  
pp. 2851-2854 ◽  
Author(s):  
Walter B. Tucker ◽  
John W. Weatherly ◽  
Duane T. Eppler ◽  
L. Dennis Farmer ◽  
Diane L. Bentley

2017 ◽  
Author(s):  
Naohiro Kosugi ◽  
Daisuke Sasano ◽  
Masao Ishii ◽  
Shigeto Nishino ◽  
Hiroshi Uchida ◽  
...  

Abstract. In September 2013, we observed an expanse of surface water with low CO2 partial pressure (pCO2sea) (


2014 ◽  
Vol 11 (23) ◽  
pp. 6769-6789 ◽  
Author(s):  
N. R. Bates ◽  
R. Garley ◽  
K. E. Frey ◽  
K. L. Shake ◽  
J. T. Mathis

Abstract. The carbon dioxide (CO2)-carbonate chemistry of sea-ice melt and co-located, contemporaneous seawater has rarely been studied in sea-ice-covered oceans. Here, we describe the CO2–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−1) and total alkalinity (TA; ∼30 to <500 μmol kg−1) of above-ice melt pond water was low compared to the co-located underlying mixed layer. The partial pressure of CO2 (pCO2) in these melt ponds was highly variable (∼<10 to >1500 μatm) with the majority of melt ponds acting as potentially strong sources of CO2 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 (CaCO3) minerals such as aragonite (Ωaragonite). 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 CO2 to the atmosphere or CO2 sinks. Below-ice interface water CO2–carbonate chemistry data also indicated substantial generation of alkalinity, presumably owing to dissolution of CaCO3 in sea-ice. The interface waters generally had lower pCO2 and higher pH/Ωaragonite than the co-located mixed layer beneath. Sea-ice melt thus contributed to the suppression of mixed-layer pCO2, thereby enhancing the surface ocean's capacity to uptake CO2 from the atmosphere. Our observations contribute to growing evidence that sea-ice CO2–carbonate chemistry is highly variable and its contribution to the complex factors that influence the balance of CO2 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.


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