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顶空气相色谱法测定海水二甲基硫和浮游植物细胞二甲基硫丙酸的研究 总被引：12，自引：2，他引：12
建立了顶空ＧＣ／ＦＰＤ测定海水中二甲基硫（ＤＭＳ）和浮游植物细胞中二甲基硫丙酸（ＤＭＳＰ）的方法，并研究盐度、温度、气液相比ＤＭＳ诸因素对ＤＭＳ顶空灵敏度的影响。该法对ＤＭＳ测定的相对标准偏差均小于６％，平均回收率为１０６％，最低检出限为２０ｎｇ／Ｌ。细胞ＤＭＳＰ先经碱作用转化为ＤＭＳ，在５０℃下作用时间不少于６ｈ，峰高与浓度的双对数线性相关系数大于０．９９。对１９９４年冬、１９９５年夏采自胶州湾 相似文献
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海洋中二甲基硫的生物生产与消费过程 总被引：4，自引：0，他引：4
DMS是海洋中最主要的挥发性有机硫化物,对全球气候变化和环境酸化产生重要影响。DMS的生物生产与消耗主要发生在海洋真光层。生物的生产与消耗被认为是海洋中DMS的主要来源和去除途径。海洋中DMS的生物生产和消耗是密切相关的,两者的速率基本保持平衡。目前,有关DMS生物生产与消费速率的测定方法有放射性同位素示踪和加抑制剂2种,后者颇受青睐,不过有关抑制机理还需进一步的研究。 相似文献
3.
Y.W. Watanabe H. Yoshinari A. Sakamoto Y. Nakano N. Kasamatsu T. Midorikawa T. Ono 《Marine Chemistry》2007,103(3-4):347-358
We proposed an empirical equation of sea surface dimethylsulfide (DMS, nM) using sea surface temperature (SST, K), sea surface nitrate (SSN, μM) and latitude (L, °N) to reconstruct the sea surface flux of DMS over the North Pacific between 25°N and 55°N: ln DMS = 0.06346 · SST − 0.1210 · SSN − 14.11 · cos(L) − 6.278 (R2 = 0.63, p < 0.0001). Applying our algorithm to climatological hydrographic data in the North Pacific, we reconstructed the climatological distributions of DMS and its flux between 25 °N and 55 °N. DMS generally increased eastward and northward, and DMS in the northeastern region became to 2–5 times as large as that in the southwestern region. DMS in the later half of the year was 2–4 times as large as that in the first half of the year. Moreover, applying our algorithm to hydrographic time series datasets in the western North Pacific from 1971 to 2000, we found that DMS in the last three decades has shown linear increasing trends of 0.03 ± 0.01 nM year− 1 in the subpolar region, and 0.01 ± 0.001 nM year− 1 in the subtropical region, indicating that the annual flux of DMS from sea to air has increased by 1.9–4.8 μmol m− 2 year− 1. The linear increase was consistent with the annual rate of increase of 1% of the climatological averaged flux in the western North Pacific in the last three decades. 相似文献
4.
The biogeochemical sulfur cycle in the marine boundary layer over the Northeast Pacific Ocean 总被引：1，自引：0，他引：1
T. S. Bates J. E. Johnson P. K. Quinn P. D. Goldan W. C. Kuster D. C. Covert C. J. Hahn 《Journal of Atmospheric Chemistry》1990,10(1):59-81
The major components of the marine boundary layer biogeochemical sulfur cycle were measured simultaneously onshore and off the coast of Washington State, U.S.A. during May 1987. Seawater dimethylsulfide (DMS) concentrations on the continental shelf were strongly influenced by coastal upwelling. Concentration further offshore were typical of summer values (2.2 nmol/L) at this latitude. Although seawater DMS concentrations were high on the biologically productive continental shelf (2–12 nmol/L), this region had no measurable effect on atmospheric DMS concentrations. Atmospheric DMS concentrations (0.1–12 nmol/m3), however, were extremely dependent upon wind speed and boundary layer height. Although there appeared to be an appreciable input of non-sea-salt sulfate to the marine boundary layer from the free troposphere, the local flux of DMS from the ocean to the atmosphere was sufficient to balance the remainder of the sulfur budget. 相似文献
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夏季黄海冷水团海域的丙烯酸分布与海洋环境因子和叶绿素a变化之间的关系 总被引：1，自引：0，他引：1
海水中主要含硫化合物β-二甲基巯基丙酸内盐(DMSP)降解可产生丙烯酸(AA)和活性气体二甲基硫(DMS)。2011年8月对黄海冷水团海域的AA及相关参量的分布特征进行了研究。结果表明,该海域表层海水中AA的浓度为0~0.208μmol/L,平均值为(0.081±0.075)μmol/L。AA的高值区出现在海域的东南部,可能是受到长江冲淡水的影响。AA的浓度总体上呈现出由南到北递增的趋势,与Chl-a较为一致,表明该海域的AA主要是由DMSP裂解产生的。表层海水中AA与温度表现出明显的负相关性。AA的垂直分布表现为:中层底层表层,这可能是产生AA的浮游植物与消耗AA的细菌共同作用的结果。海域中AA浓度与DMSP或DMS无明显的相关性。AA浓度远高于DMS,AA/DMS平均为106∶1,初步估算出DMSP降解产生的AA约为66.5%。AA/Chl-a平均为126.6 mmol/g,比DMSP/Chl-a高1个数量级,比DMS/Chl-a高2个数量级。 相似文献
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本文综述了目前国内外有关海水中二甲基硫（ＤＭＳ）的测定方法及其来源的研究,指出ＤＭＳＰ是海洋生物降解产生ＤＭＳ的主要来源。 相似文献
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P.D. Tortell C. Guéguen M.C. Long C.D. PayneP. Lee G.R. DiTullio 《Deep Sea Research Part I: Oceanographic Research Papers》2011,58(3):241-259
We report results from two surveys of pCO2, biological O2 saturation (??O2/Ar) and dimethylsulfide (DMS) in surface waters of the Ross Sea polynya. Measurements were made during early spring (November 2006-December 2006) and mid-summer (December 2005-January 2006) using ship-board membrane inlet mass spectrometry (MIMS) for high spatial resolution (i.e. sub-km) analysis. During the early spring survey, the polynya was in the initial stages of development and exhibited a rapid increase in open water area and phytoplankton biomass over the course of our ∼3 week occupation. We observed a rapid transition from a net heterotrophic ice-covered system (supersaturated pCO2 and undersaturated O2) to a high productivity regime associated with a Phaeocystis-dominated phytoplankton bloom. The timing of the early spring phytoplankton bloom was closely tied to increasing sea surface temperature across the polynya, as well as reduced wind speeds and ice cover, leading to enhanced vertical stratification. There was a strong correlation between pCO2, ??O2/Ar, DMS and chlorophyll a (Chl a) during the spring phytoplankton bloom, indicating a strong biological imprint on gas distributions. Box model calculations suggest that pCO2 drawdown was largely attributable to net community production, while gas exchange and shoaling mixed layers also exerted a strong control on the re-equilibration of mixed layer ??2 with the overlying atmosphere. DMS concentrations were closely coupled to Phaeocystis biomass across the early spring polynya, with maximum concentrations exceeding 100 nM.During the summer cruise, we sampled a large net autotrophic polynya, shortly after the seasonal peak in phytoplankton productivity. Both diatoms and Phaeocystis were abundant in the phytoplankton assemblages during this time. Minimum pCO2 was less than 100 ppm, while ??O2/Ar exceeded 30% in some regions. Mean DMS concentrations were ∼2-fold lower than during the spring, although the range of concentrations was similar between the two surveys. There was a significant correlation between pCO2, ??O2/Ar and Chl a across the summer polynya, but the strength of these correlations and the slope of O2 vs. CO2 relationship were significantly lower than during the early spring. Summertime DMS concentrations were not significantly correlated to phytoplankton biomass (Chl a), pCO2 or ??O2/Ar. In contrast to the early spring time, there were no clear temporal trends in summertime gas concentrations. Rather, small-scale spatial variability, likely resulting from mixing and localized sea-ice melt, was clearly evident in surface gas distributions across the polynya. Analysis of length-scale dependent variability demonstrated that much of the spatial variance in surface water gases occurred at scales of <20 km, suggesting that high resolution analysis is needed to fully capture biogeochemical heterogeneity in this system. 相似文献
8.
Kazushi Aranami Shuichi Watanabe Shizuo Tsunogai Masato Hayashi Ken Furuya Toshi Nagata 《Journal of Oceanography》2001,57(3):315-322
Dimethylsulfide (DMS), chlorophyll a (Chl-a), accessory pigments (fucoxanthin, peridinin and 19-hexanoyloxyfucoxanthin), and bacterial production (BP) were measured in the surface layer (0–100 m) of the subarctic North Pacific, including the Bering Sea, during summer (14 July–5 September, 1997). In surface sewater, the concentrations of DMS and Chl-a varied widely from 1.3 to 13.2 nM (5.1 ± 3.0 nM, mean ± S.D., n = 48) and from 0.1 to 2.4 µg L–1 (0.6 ± 0.6 µg L–1, n = 24), respectively. In the subarctic North Pacific, DMS to Chl-a ratios (DMS/Chl-a) were higher on the eastern side than the western side (p < 0.0001). Below the euphotic zone, DMS/Chl-a ratios were law and the correlation between DMS and Chl-a was relatively strong (r
2 = 0.700, n = 27, p < 0.0001). In the euphotic zone, DMS/Chl-a ratios were higher and the correlation between DMS and Chl-a was weak (r
2 = 0.128, n = 50, p = 0.01). The wide variation in DMS/Chl-a ratios would be at least partially explained by the geographic variation in the taxonomic composition of phytoplankton, because of the negative correlation between DMS/Chl-a and fucoxanthin-to-Chl-a ratios (Fuc/Chl-a) (r
2 = 0.476, n = 26, p = 0.0001). Furthermore, there was a positive correlation between DMS and BP (r
2 = 0.380, n = 19, p = 0.005). This suggests that BP did not represent DMS and dimethylsulfoniopropionate (DMSP) removal by bacterial consumption but rather DMSP degradation to DMS by bacterial enzyme. 相似文献
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