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1.
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
2.
Takushi Niki Miwa Shimizu Ayako Fujishiro Junji Kinoshita 《Journal of Oceanography》2007,63(5):873-877
During time-series observations in Sagami Bay, Japan, the concentration of dissolved dimethylsulfoniopropionate (DMSPd), a precursor of dimethylsulfide (DMS), was negatively correlated with salinity. In the laboratory, low-salinity shock reduced
DMS production rates of the natural bacterial community and induced rapid DMSP release from a dinophyte, Heterocapsa triquetra, suggesting that low-salinity shock reduced DMSPd consumption but enhanced DMSPd production, which agrees with the negative correlation between DMSPd and salinity observed in Sagami bay. In addition, low-salinity shock did not affect DMSP lyase activity of H. triquetra. Low-salinity shock would increase the contribution from algae in DMS production, leading to an increase in potential DMS
productivity in the environment. 相似文献
3.
Takushi?NikiEmail author Taiki?Fujinaga Mariyo?F.?Watanabe Junji?Kinoshita 《Journal of Oceanography》2004,60(5):913-917
Solid-phase microextraction (SPME) is a simple, sensitive and less destructive method for the determination of dimethylsulfide
(DMS) in seawater. Combined with detection by gas chromatography-mass spectrometry (GC-MS), the method had sufficient sensitivity
(minimum detectable concentration of DMS was 0.05 nM), and practical levels of reproducibility (relative standard deviation
≤7%) and linearity (r
2 > 0.995) over a wide concentration range (0.5 to 910 nM). The protocol developed was applied to a Sagami Bay water sample
to determine concentrations of DMS and DMSP, and in situ DMSP-lyase activity. 相似文献
4.
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
5.
J. P. Putaud N. Mihalopoulos B. C. Nguyen J. M. Campin S. Belviso 《Journal of Atmospheric Chemistry》1992,15(2):117-131
Daily measurements of atmospheric sulfur dioxide (SO2) concentrations were performed from March 1989 to January 1991 at Amsterdam Island (37°50 S–77°30 E), a remote site located in the southern Indian Ocean. Long-range transport of continental air masses was studied using Radon (222Rn) as continental tracer. Average monthly SO2 concentrations range from less than 0.2 to 3.9 nmol m-3 (annual average = 0.7 nmol m-3) and present a seasonal cycle with a minimum in winter and a maximum in summer, similar to that described for atmospheric DMS concentrations measured during the same period. Clear diel correlation between atmospheric DMS and SO2 concentrations is also observed during summer. A photochemical box model using measured atmospheric DMS concentrations as input data reproduces the seasonal variations in the measured atmospheric SO2 concentrations within ±30%. Comparing between computed and measured SO2 concentrations allowed us to estimate a yield of SO2 from DMS oxidation of about 70%. 相似文献
6.
Daily measurements of atmospheric concentrations of dimethylsulfide (DMS) were carried out for two years in a marine site at remote area: the Amsterdam Island (37°50S–77°31E) located in the southern Indian Ocean. DMS concentrations were also measured in seawater. A seasonal variation is observed for both DMS in the atmosphere and in the sea-surface. The monthly averages of DMS concentrations in the surface coastal seawater and in the atmosphere ranged, respectively, from 0.3 to 2.0 nmol l-1 and from 1.4 to 11.3 nmol m-3 (34 to 274 pptv), with the highest values in summer. The monthly variation of sea-to-air flux of DMS from the southern Indian Ocean ranges from 0.7 to 4.4 mol m-2 d-1. A factor of 2.3 is observed between summer and winter with mean DMS fluxes of 3.0 and 1.3 mol m-2 d-1, respectively. 相似文献
7.
Simulations of seasonal variations of sulfur compounds in the remote marine atmosphere 总被引:1,自引:0,他引:1
A photochemical box model is used to simulate seasonal variations in concentrations of sulfur compounds at latitude 40° S. It is assumed that the hydroxyl radical (OH) addition reaction to sulfur in the dimethyl sulfide (DMS) molecule is the predominant pathway for methanesulfonic acid (MSA) production, and that the rate constant increases as the air temperature decreases. Concentration of the nitrate radical (NO3) is a function of the DMS flux, because the reaction of DMS with NO3 is the most important loss mechanism of NO3. While the diurnally averaged concentration of OH in winter is a factor of about 8 smaller than in summer, due to the weak photolysis process, the diurnally averaged concentration of NO3 in winter is a factor of about 4–5 larger than in summer, due to the decrease of DMS flux. Therefore, at middle and high latitudes in winter, atmospheric DMS is mainly oxidized by the reaction with NO3. The calculated ratio of the MSA to SO2 production rates is smaller in winter than in summer, and the MSA to non-sea-salt sulfate (nssSO4
2-) molar ratio varies seasonally. This result agrees with data on the seasonal variation of the MSA/nssSO4
2- molar ratio obtained at middle and high latitudes. The calculations indicate that during winter the reaction of DMS with NO3 is likely to be a more important sink of NOx (NO+NO2) than the reaction of NO2 with OH, and to serve as a significant pathway of the HNO3 production. If dimethyl sulfoxide (DMSO) is produced through the OH addition reaction and is heterogeneously oxidized in aqueous solutions, half of the nssSO4
2- produced in summer may be through the oxidation process of DMSO. It is necessary to further investigate the oxidation products by the reaction of DMS with OH, and the possibility of the reaction of DMS with NO3 during winter. 相似文献
8.
Veli-Matti Kerminen Risto E. Hillamo Anthony S. Wexler 《Journal of Atmospheric Chemistry》1998,30(3):345-370
A box model was constructed to investigate connections between the particulate MSA to non-sea-salt sulfate ratio, R, and DMS chemistry in a clean marine boundary layer. The simulations demonstrated that R varies widely with particle size, which must be taken into account when interpreting field measurements or comparing them with each other. In addition to DMS gas-phase chemistry, R in the submicron size range was shown to be sensitive to the factors dictating sulfate production via cloud processing, to the removal of SO2 from the boundary layer by dry deposition and sea-salt oxidation, to the entrainment of SO2 from the free troposphere, to the relative concentration of sub- and supermicron particles, and to meteorology. Three potential explanations for the increase of R toward high-latitudes during the summer were found: larger MSA yields from DMS oxidation at high latitudes, larger DMSO yields from DMS oxidation followed by the conversion of DMSO to MSA at high latitudes, or lower ambient H2O2 concentrations at high latitudes leading to less efficient sulfate production in clouds. Possible reasons for the large seasonal amplitude of R at mid and high latitudes include seasonal changes in the partitioning of DMS oxidation to the OH and NO3 initiated pathways, seasonal changes in the concentration of species participating the DMS-OH reaction pathway, or the existence of a SO2 source other than DMS oxidation in the marine boundary layer. Even small anthropogenic perturbations were shown to have a potential to alter the MSA to non-sea-salt sulfate ratio. 相似文献
9.
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
10.
于2010年7~11月对胶州湾夏、秋季浮游动物种类和丰度进行现场调查,并分析讨论了胶州湾夏、秋季浮游动物丰度的水平分布与环境因子(温度、盐度、水深、叶绿素a)和二甲基硫(DMS)、溶解态β-二甲基巯基丙酸内盐(DMSPd)、颗粒态β-二甲基巯基丙酸内盐(DMSPp)的相关性。结果表明,胶州湾浮游动物丰度分布不均匀,8月湾内西部沿岸海域C1站位出现调查期间的动物丰度最大值(656.1ind/m3),最小值(1.492ind/m3)出现在10月胶州湾东北部的A2站位。浮游动物丰度具有明显的季节变化,秋季浮游动物丰度低于夏季浮游动物丰度。浮游动物丰度与盐度、叶绿素a含量、细菌生物量的相关性不明显,2010年10月浮游动物丰度与DMS呈显著正相关(P0.05),11月的浮游动物丰度与DMSPp呈显著正相关(P0.05),其它月份(7、8、9月)的浮游动物丰度与DMS、DMSPd、DMSPp浓度的相关性均不明显。由于浮游动物摄食活动对DMS释放的影响受多种因素的制约,因此浮游动物与DMS的相互作用需要进一步研究。 相似文献