Variation of dimethylsulfide mixing ratio over the Southern Ocean from 36°S to 70°S

AbstractAtmospheric dimethylsulfide (DMS) was measured to investigate the variation in its concentration over sea ice free oceans and sea ice regions of the Southern Ocean, using a proton transfer reaction-mass spectrometer (PTR-MS) on board the icebreaker Shirase from 1 December 2009 to 16 March 2010. In general, DMS concentrations over sea ice regions were very low compared with those over the sea ice free ocean. However, abrupt increases in DMS concentrations occurred over sea ice regions while the ship was moving and crushing the sea ice. Undoubtedly, the elevated DMS concentrations were caused by large DMS emissions from gaps in the ice made by the ship. During the period when Shirase had anchored off Syowa Station (69°00.4′S, 39°35.3′E), Antarctica, DMS concentrations were not detected. At this time, the surrounding sea of East Ongul island, on which Syowa Station is located, was completely covered with multi-year fast ice. Sea ice probably inhibits DMS emission from the ocean to the atmosphere. In addition, there was no evidence that chlorophyll a concentration in the sea water or wind speed above the sea surface affect atmospheric DMS concentrations over the sea ice free ocean regions

How to process sea ice for chlorophyll-based photosynthesis measurement of the ice algae?

The Tenth Symposium on Polar Science/Ordinary sessions: [OB] Polar Biology, Wed. 4 Dec. / 3F Multipurpose conference room, National Institute of Polar Researc

Methane release from open leads and new ice following an Arctic winter storm event

We examine an Arctic winter storm event, which led to ice break–up, the formation of open leads, and the subsequent freezing of these leads. The methane (CH4) concentration in under–ice surface water before and during the storm event was 8–12 nmol L−1, which resulted in a potential sea–to–air CH4 flux ranging from +0.2 to +2.1 mg CH4 m−2 d−1 in open leads. CH4 ventilation between seawater and atmosphere occurred when both open water fraction and wind speed increased. Over the nine days after the storm, sea ice grew 27 cm thick. Initially, CH4 concentrations in the sea ice brine were above the equilibrium with the atmosphere. As the ice grew thicker, most of the CH4 was lost from upper layers of sea ice into the atmosphere, implying continued CH4 evasion after the leads were ice–covered. This suggests that wintertime CH4 emissions need to be better constrainedMethane release from open leads and new ice following an Arctic winter storm eventacceptedVersio

Methane release from open leads and new ice following an Arctic winter storm event

We examine an Arctic winter storm event, which led to ice break–up, the formation of open leads, and the subsequent freezing of these leads. The methane (CH4) concentration in under–ice surface water before and during the storm event was 8–12 nmol L−1, which resulted in a potential sea–to–air CH4 flux ranging from +0.2 to +2.1 mg CH4 m−2 d−1 in open leads. CH4 ventilation between seawater and atmosphere occurred when both open water fraction and wind speed increased. Over the nine days after the storm, sea ice grew 27 cm thick. Initially, CH4 concentrations in the sea ice brine were above the equilibrium with the atmosphere. As the ice grew thicker, most of the CH4 was lost from upper layers of sea ice into the atmosphere, implying continued CH4 evasion after the leads were ice–covered. This suggests that wintertime CH4 emissions need to be better constrained

Cnm of Streptococcus mutans is important for cell surface structure and membrane permeability

Streptococcus mutans, a Gram-positive facultative anaerobic bacterium, is a major pathogen of dental caries. The protein Cnm of S. mutans is involved in collagen binding, but its other biological functions are unknown. In this study, a Cnm-deficient isogenic mutant and a complementation strain were generated from a Cnm-positive S. mutans strain to help determine the properties of Cnm. Initially, comparison of the cell surface structure was performed by electron microscopy, which demonstrated that Cnm appears to be localized on the cell surface and associated with a protruding cell surface structure. Deep RNA sequencing of the strains revealed that the defect in Cnm caused upregulated expression of many genes related to ABC transporters and cell-surface proteins, while a few genes were downregulated. The amount of biofilm formed by the Cnm-defective strain increased compared with the parental and complemented strains, but the biofilm structure was thinner because of elevated expression of genes encoding glucan synthesis enzymes, leading to increased production of extracellular polysaccharides. Particular antibiotics, including bacitracin and chloramphenicol, had a lower minimum inhibitory concentration for the Cnm-defective strain than particular antibiotics, including bacitracin and chloramphenicol, compared with the parental and complemented strains. Our results suggest that S. mutans Cnm is located on the cell surface, gives rise to the observed protruding cell surface, and is associated with several biological properties related to membrane permeability

Aerosol nucleation observed in JARE51

第2回極域科学シンポジウム　共通セッション「海氷圏の生物地球化学」 11月16日（水） 統計数理研究所 3階リフレッシュフロ

Isotope measurements of the Arctic water cycle and exchange processes between seawater, sea ice, and snow during MOSAiC

For the past two decades, the Arctic water cycle changed rapidly due to surface air temperatures (SATs) increasing at twice the global rate. Terrestrial ice (i.e. Greenland Ice Sheet) and marine sea-ice loss, alterations of ocean circulation patterns, and shifting atmospheric moisture sources and transport are some of the most pronounced changes caused by the Arctic amplification, fostering increased humidity levels. Stable water isotopes (δ18O, δ2H) and the secondary parameter d-excess are valuable tracers for hydrological changes, including how these shifts may affect the global climate system. However, it is only recently that we are using precipitation and water vapor networks to resolve water isotope patterns and processes in the Arctic. However, a fully coordinated study of the entire water cycle attributes year-long including sea ice, ocean water, vapor, and precipitation has until recently has been absent. The Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition provided a unique opportunity to collect, analyze, and synthesize discrete samples of the different hydrological compartments in the central Arctic, covering a complete one-year seasonal cycle using a combination of ship-based, the pan-Arctic Water Isotope Network (PAPIN). These observations can lead to new insights into coupled ocean-atmosphere climate processes operating in the Arctic, especially during extreme events, sea ice formation, sea ice retreat, and during a dichotomy of synoptic weather patterns over the MOSAiC-year. We present the isotopic traits of more than 2,200 discrete samples (i.e., seawater, sea ice, snow, brines, frost flowers, lead ice, ridge ice, and precipitation) collected during MOSAiC. Snow has the most depleted δ18O values (-16.3 ± 9.1‰; the number of samples N=306), whereas seawater is the most enriched δ18O compartment (-1.5 ± 0.9‰; N=302) of the Arctic water cycle. Precipitation throughout the Arctic Basin varied from -10‰ to -35‰. Snow profiles are gradually enriched in δ18O from top to bottom by ~20‰ partially due to sublimation of deposited snow, as well as snow metamorphism and its effects on the water isotopes. Second-year ice (SYI) is isotopically relatively depleted in δ18O (-4.2 ± 2.6‰; N=200) compared to first-year ice (FYI) (-0.7 ± 2.1‰; N=635) and insulated FYI (i.e. FYI grown at the bottom of SYI) (-1.7 ± 2.4‰; N=214). The latter is likely caused by post-depositional exchange processes with snow. Open water leads (-1.6 ± 2.4‰; N=137) and melt ponds (-2.1 ± 2.7‰; N=109) on the surface of sea ice contribute to the moistening of the atmosphere in the Arctic on a regional scale. Our dataset provides an unprecedented snapshot of the present-day isotopic composition of the Arctic water cycle during an entire year. The coupling of these discrete samples data with the continuous measurements of atmospheric water vapor may shed light on the relative contribution of snow, sea ice, seawater, open water leads, and melt ponds both spatially and temporally to regional and local moisture levels in the Arctic. Stable water isotopes will ultimately contribute to resolving the linkages between sea ice, ocean, and atmosphere during the critical transition from frozen ocean to open water conditions

南大洋インド洋区季節海氷域における溶存炭酸物質の季節変化

第6回極域科学シンポジウム分野横断セッション：[IB1] 海氷域における生物地球化学的研究11月17日（火）　統計数理研究所 セミナー室1（D305