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1.
Sixteen surface microlayer samples and corresponding subsurface water samples were collected in the western North Atlantic during April–May 2003 to study the distribution and cycling of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) and the factors influencing them. In the surface microlayer, high concentrations of DMS appeared mostly in the samples containing high levels of chlorophyll a, and a significant correlation was found between DMS and chlorophyll a concentrations. In addition, microlayer DMS concentrations were correlated with microlayer DMSPd (dissolved) concentrations. DMSPd was found to be enriched in the microlayer with an average enrichment factor (EF) of 5.19. However, no microlayer enrichment of DMS was found for most samples collected. Interestingly, the DMS production rates in the microlayer were much higher than those in the subsurface water. Enhanced DMS production in the microlayer was likely due to the higher concentrations of DMSPd in the microlayer. A consistent pattern was observed in this study in which the concentrations of DMS, DMSPd, DMSPp (particulate) and chlorophyll a in the microlayer were closely related to their corresponding subsurface water concentrations, suggesting that these constituents in the microlayer were directly dependent on the transport from the bulk liquid below. Enhanced DMS production in the microlayer further reinforces the conclusion that the surface microlayer has greater biological activity relative to the underlying water.  相似文献   

2.
Spatial variations in dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) were surveyed in the surface microlayer and in the subsurface waters of the low productivity South China Sea in May 2005. Overall, average subsurface water concentrations of DMS and DMSP of dissolved (DMSPd) and particulate (DMSPp) fractions were 1.74 (1.00-2.50), 3.92 (2.21-6.54) and 6.06 (3.40-8.68) nM, respectively. No enrichment in DMS and DMSPp was observed in the microlayer. In contrast, the microlayer showed a DMSPd enrichment, with an average enrichment factor (EF, defined as the ratio of the microlayer concentration to subsurface water concentration) of 1.40. In the study area, none of the sulfur components were correlated with chlorophyll a. An important finding in this study was that DMS, DMSP and chlorophyll a concentrations in the surface microlayer were respectively correlated with those in the subsurface water, suggesting a close linkage between these two water bodies. The ratios of DMS:Chl-a and DMSPp:Chl-a showed a gradually increasing trend from North to South. This might be due to changes in the proportion of DMSP producers in the phytoplankton community with the increased surface seawater temperature. A clear diurnal variation in the DMS and DMSP concentrations was observed at an anchor station with the highest concentrations appearing during the day and the lowest concentrations during the night. The higher DMS and DMSP concentrations during daytime might be attributed to the light-induced increase in both algal synthesis and exudation of DMSP and biological production of DMS. The mean flux of DMS from the investigated area to the atmosphere was estimated to be 2.06 micromo lm(-2)d(-1). This low DMS emission flux, together with the low DMS surface concentrations was attributed to the low productivity in this sea.  相似文献   

3.
Temporal distributions of dimethylsulfide(DMS) and dimethylsulfoniopropionate(DMSP) were studied in the southern Yellow Sea(SYS) during April and September 2010. The mean concentrations(range) of DMS, dissolved and particulate DMSP(DMSPd and DMSPp) in the surface waters in spring are 1.69(0.48–4.92), 3.18(0.68–6.75)and 15.81(2.82–52.33) nmol/L, respectively, and those in autumn are 2.80(1.33–5.10), 5.45(2.19–11.30) and 30.63(6.24–137.87) nmol/L. On the whole, the distributions of DMS and DMSP in spring are completely different from those in autumn. In the central part of the SYS, the concentrations of DMS and DMSP in spring are obviously higher than those in autumn, but the opposite situation is found on the south of 34°N, which can be attributed to the differences in nutrients and phytoplankton biomass and composition between spring and autumn. Besides,the seasonal variations of water column stability and the Changjiang diluted water also have significant impact on the distributions of DMS and DMSP in spring and autumn on the south of 34°N. DMS and DMSPp concentrations coincide well with chlorophyll a(Chl a) levels in the spring cruise, suggesting that phytoplankton biomass may play an important role in controlling the distributions of DMS and DMSPp in the study area. Annual DMS emission rates range from 0.015 to 0.033 Tg/a(calculated by S), respectively, using the equations of Liss and Merlivat(1986) and Wanninkhof(1992). This result implies a significant relative contribution of the SYS to the global oceanic DMS fluxes.  相似文献   

4.
于2012年7—9月现场测定了北极挪威海和格陵兰海区域海水二甲基硫(DMS)及其前体物质二甲巯基丙酸内盐(DMSP,分溶解态DMSPd和颗粒态DMSPp)的含量,研究了其空间分布格局及其影响因素,探讨了表层海水DMS的生物周转和去除途径。结果表明,表层海水DMS、DMSPd和DMSPp的平均浓度分别为5.36nmol/L、15.63nmol/L和96.73nmol/L,受挪威海流和北极深层水影响,表层海水二甲基硫化物浓度呈现出由低纬度向高纬度海域递减的趋势。DMSPd和DMSPp浓度与Chl a浓度均有显著的相关性,说明浮游植物生物量是影响挪威海和格陵兰海二甲基硫化物生产的重要因素。表层海水DMS生物生产和消费速率平均值分别为18.19nmol/(L·d)、15.67nmol/(L·d)。DMS微生物周转时间变化范围为0.03~1.80d,平均值为0.49d,DMS海-气周转时间是微生物消费时间的90倍,说明夏季挪威海和格陵兰海表层海水中DMS微生物消费过程是比海-气扩散更具优势的去除机制。  相似文献   

5.
以胶州湾及青岛近海为研究区域,利用吹扫-捕集气相色谱法研究了二甲基硫(DMS)和二甲巯基丙酸(DMSP,分为溶解态DMSPd和颗粒态DMSPp)在微表层与次表层中的浓度以及它们在微表层中的富集行为。结果表明,DMS、DMSPd和DMSPp在微表层中的浓度高于次表层,它们在微表层中的富集因子分别为1.17、1.84和1.51。研究发现,DMS及DMSPp浓度与叶绿素a(Chl-a)浓度有很好的相关性,但它们的周日变化与Chl-a并不完全同步。DMS/Chl-a和DMSPp/Chl-a的比值在次表层和微表层分别为4.35、13.47mmol/g和3.99、15.88mmol/g。胶州湾及青岛近海生态环境受人为活动干扰严重,使本海域DMS含量较高,从而贡献出较大的DMS海-气通量。  相似文献   

6.
Twenty-eight sea surface microlayer samples, along with subsurface bulk water samples were collected in Funka Bay, Japan during October 2000–March 2001 and analyzed for dimethylsulfoniopropionate, dissolved (DMSPd) and particulate (DMSPp), and chlorophyll a. The aim of the study was to examine the extent of enrichment of DMSP in the microlayer and its relationship to chlorophyll a, as well as the production rate of dimethylsulfide (DMS) from DMSP and the factors that influence this. The enrichment factor (EF) of DMSPd in the surface microlayer ranged from 0.81 to 4.6 with a mean of 1.85. In contrast, EF of DMSPp in the microlayer varied widely from 0.85–10.5 with an average of 3.21. Chlorophyll a also appeared to be enriched in the microlayer relative to the subsurface water. This may be seen as an important cause of the observed enrichment of DMSP in the microlayer. The concentrations of DMSPp in the surface microlayer showed a strong temporal variation, basically following the change in chlorophyll a levels. Moreover, the microlayer concentrations of DMSPp were, on average, 3-fold higher than the microlayer concentrations of DMSPd and there was a significant correlation between them. Additionally, there was a great variability in the ratios of DMSPp to chlorophyll a over the study period, reflecting seasonal variation in the proportion of DMSP producers in the total phytoplankton assemblage. It is interesting that the production rate of DMS was enhanced in the microlayer and this rate was closely correlated with the microlayer DMSPd concentration. Microlayer enrichment of chlorophyll a and higher DMS production rate in the microlayer provide favorable evidence supporting the view that the sea surface microlayer has a greater biological activity than the underlying water.  相似文献   

7.
The production of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) by marine microalgae was investigated to elucidate more on the role of marine phytoplankton in ocean-atmosphere interactions in the global biogeochemical sulfur cycle.Axenic laboratory cultures of four marine microalgae–Isochrysis galbana 8701,Pavlova viridis,Platymonas sp.and Chlorella were tested for DMSP production and conversion into DMS.Among these four microalgae,Isochrysis galbana 8701 and Pavlova viridis are two species of Haptophyta,while Chlorella and Platymonas sp.belong to Chlorophyta.The results demonstrate that the four algae can produce various amounts of DMS(P),and their DMS(P) production was species specific.With similar cell size,more DMS was released by Haptophyta than that by Chlorophyta.DMS and dissolved DMSP (DMSPd) concentrations in algal cultures varied significantly during their life cycles.The highest release of DMS appeared in the senescent period for all the four algae.Variations in DMSP concentrations were in strong compliance with variations in algal cell densities during the growing period.A highly significant correlation was observed between the DMS and DMSPd concentrations in algal cultures,and there was a time lag for the variation trend of the DMS concentrations as compared with that of the DMSPd.The consistency of variation patterns of DMS and DMSPd implies that the DMSPd produced by phytoplankton cells has a marked effect on the production of DMS.In the present study,the authors’ results specify the significant contribution of the marine phytoplankton to DMS(P) production and the importance of biological control of DMS concentrations in oceanic water.  相似文献   

8.
本研究首次探究了西太平洋雅浦海沟北段从表层到超深渊海水中甲烷（CH4）及二甲基硫（DMS）的前体物质二甲基巯基丙酸内盐（DMSP）的浓度变化情况。结果表明:雅浦海沟海水甲烷浓度变化范围为1.49~3.87 nmol/L。其上层海水甲烷平均浓度最高,有明显的次表层极大现象。雅浦海沟氧最小层海水的甲烷平均浓度最低;在500~1 000 m中层水中甲烷浓度有一定程度的增大,1 000 m以下至底层甲烷浓度继续升高。研究海区溶解态DMSP（DMSPd）和总DMSP（DMSPt）平均浓度的垂直变化随深度呈先增大后减小趋势,颗粒态DMSP（DMSPp）的平均浓度随深度呈波动式变化,在中层达到最大。雅浦海沟CH4和DMSP浓度垂直变化受浮游生物、微生物、光照、温度、压力、大洋环流等的复杂影响。在真光层海水中,CH4浓度与DMSPd、DMSPp和DMSPt浓度表现为负相关关系,在200 m至底层海水中,CH4浓度与DMSPd、DMSPp和DMSPt浓度表现为正相关关系,显示光照条件是造成雅浦海沟不同深度海水CH4和DMSP浓度相关性差异的关键因素。  相似文献   

9.
Dimethylsulfide enrichment in the surface microlayer of the South China Sea   总被引：5，自引：0，他引：5  
A total of 22 sea surface microlayer samples collected from the Nansha Islands waters of the South China Sea were analyzed for dimethylsulfide (DMS), chlorophyll a and nutrients including nitrate, phosphate and silicate. The DMS concentrations in surface microlayer samples ranged from 82 to 280 ng S/l with a mean of 145 ng S/l. A significant correlation was found between DMS and chlorophyll a data both in the surface microlayer as well as in the subsurface water. However, no correlation was observed between DMS and nutrient concentrations in the surface microlayer. The DMS concentrations were higher in all surface microlayer samples, compared with subsurface samples. The enrichment factor (EF) of DMS in the surface microlayer varied from 1.21 to 3.08 with an average of 1.95. The EF of DMS was significantly correlated with that of chlorophyll a in the microlayer. The enrichment of DMS in the microlayer may be due to two factors, including the in situ production from phytoplankton and the transportation from the underlying seawater. The diel variations in DMS and chlorophyll a concentrations were studied at a fixed station. The highest concentrations of DMS in the surface microlayer and subsurface water were simultaneously observed in the late afternoon (1800 h), while the highest levels of chlorophyll a were simultaneously found at night (0200 h).  相似文献   

10.
The impact of in situ iron fertilisation on the production of particulate dimethylsulphoniopropionate (DMSPp) and its breakdown product dimethyl sulphide (DMS) was monitored during the SOLAS air-sea gas exchange experiment (SAGE). The experiment was conducted in the high nitrate, low chlorophyll (HNLC) waters of the sub-Antarctic Southern Ocean (46.7°S 172.5°E) to the south-east of New Zealand, during March-April, 2004. In addition to monitoring net changes in the standing stocks of DMSPp and DMS, a series of dilution experiments were used to determine the DMSPp production and consumption rates in relation to increased iron availability. In contrast to previous experiments in the Southern Ocean, DMS concentrations decreased over the course of the 15-d iron-fertilisation experiment, from an integrated volume-specific concentration in the mixed layer on day 0 of 0.78 nM (measured values 0.65-0.91 nM) to 0.46 nM (measured values 0.42-0.47 nM) by day 15, in parallel with the surrounding waters. DMSPp, chlorophyll a and the abundance of photosynthetic picoeukaryotes exhibited indiscernible or only moderate increases in response to the raised iron availability, despite an obvious physiological response by the phytoplankton. High specific growth rates of DMSPp, equivalent to 0.8-1.2 doublings d−1, occurred at the simulated 60% light level of the dilution experiments. Despite the high production rates, DMSPp accumulation was suppressed in part by microzooplankton grazers who consumed between 61% d−1 and 126% d−1 of the DMSPp production. Temporal trends in the rates of production and consumption illustrated a close coupling between the DMSP-producing phytoplankton and their microzooplankton grazers. Similar grazing and production rates were observed for the eukaryotic picophytoplankton that dominated the phytoplankton biomass, partial evidence that picoeukaryotes contributed a substantial proportion of the DMSP synthesis. These rates for DMSPp and picoeukaryotes were considerably higher than for chlorophyll a, indicating higher cycling rates of the DMSP-producing taxa than for the bulk phytoplankton community. When compared to the total phytoplankton community, there was no evidence of selection against the DMSP-containing phytoplankton by the microzooplankton grazers; the opposite appeared to be the case. SAGE demonstrated that increased iron availability in the HNLC waters of the Southern Ocean does not invariably lead to enhanced DMS sea-air flux. The potential suppression of DMSPp accumulation by grazers needs to be taken into account in future attempts to elevate DMS emission through in situ iron fertilisation and in understanding the hypothesised link between levels of Aeolian iron deposition in the Southern Ocean, DMS emission and global albedo.  相似文献   

11.
黄、渤海二甲基硫化物的浓度分布与迁移转化速率研究   总被引：2，自引：1，他引：1  
于2015年8-9月对黄、渤海海域进行现场调查,研究了海水中二甲基硫（DMS）、β-二甲巯基丙酸内盐（DMSP）、二甲亚砜（DMSO）的浓度分布、相互关系及影响因素,测定了DMS的生物生产与消耗、光化学氧化和海-气扩散速率,对DMS的迁移转化速率进行综合评价。结果表明:表层海水中DMS、溶解态DMSP（DMSPd）、颗粒态DMSP（DMSPp）、溶解态DMSO（DMSOd）和颗粒态DMSO（DMSOp）浓度的平均值分别为（6.12±3.01）nmol/L、（6.03±3.45）nmol/L、（19.47±9.15）nmol/L、（16.85±8.34）nmol/L和（14.37±7.47）nmol/L,整体呈现近岸高远海低,表层高底层低的趋势。DMS、DMSPd和DMSOp浓度与叶绿素（Chl a）浓度存在显著的相关性。表层海水中DMS光氧化速率顺序为:kUVA > kUVB > k可见,其中UVA波段占光氧化的70.8%。夏季黄、渤海微生物消耗、光氧化及海-气扩散对DMS去除的贡献率分别为32.4%、34.5%和33.1%,表明3种去除途径作用相当。黄、渤海DMS海-气通量变化范围为0.79~48.45 μmol/（m2·d）,平均值为（11.87±11.35）μmol/（m2·d）。  相似文献   

12.
黄海冷水团水域浮游植物群落粒级结构的季节变化   总被引：4，自引：0，他引：4  
根据2006—2007年度4个季节航次的实测资料,分析了黄海冷水团水域浮游植物叶绿素及其粒级结构的时空分布特征及季节变化规律,结果表明,在研究海域30 m以浅叶绿素总量的平均含量从高到低的顺序为:春季的(1.01 mg/m3)、夏季的(0.81 mg/m3)、秋季(0.72 mg/m3)、冬季(0.68 mg/m3);在叶绿素浓度大于1 mg/m3和小于1 mg/m3的区域浮游植物粒级结构差异较大,在整个研究海域,粒径较小的微型和微微型浮游植物对总生物量的贡献始终占主导(65%),粒径较大的小型浮游植物在冬季和春季贡献率相对较高;从季节尺度看,浮游植物的平均粒级指数从大到小的顺序为:春季的(15.47μm),冬季的(11.08μm),秋季的(8.61μm),夏季的(6.52μm);尽管不同季节水文和化学环境差异显著,但是不同粒径浮游植物的贡献率随总生物量的变化表现出一致性的规律。对环境因子与叶绿素分布的相关分析表明,浮游植物的生长在夏季主要受到营养盐来源的限制,冬季主要受到水体混合引起的光照限制,秋季可能受到磷酸盐和水体混合的共同限制。浮游植物粒级结构的分布格局主要是由各组分在不同环境中的资源竞争优势决定的。  相似文献   

13.
Data on the distribution of dimethylsulphide (DMS) and dimethylsulphoniopropionate (DMSP) in relation to phytoplankton abundance in different oceanic environments is important to understand the biogeochemistry of DMS, which plays an important role in the radiation balance of the earth. During the summer monsoon of 2001 measurements were made for DMS and DMSPt (total DMSP) together with related biological parameters in the Bay of Bengal. Both DMS and DMSPt were restricted to the upper 40 m of the water column. Diatoms accounted for more than 95% of the phytoplankton and were the major contributors to the DMS and DMSPt pool. The mean concentration of DMS in the upper 40 m was observed to be around 1.8+/-1.9 nM in the study area, while DMSPt concentrations varied between 0.7 nM and 40.2 nM with a mean of 10.4+/-8.2 nM. The observed lower DMSPt in the northern Bay in spite of higher mean primary productivity, chlorophyll a and phytoplankton cell counts seemed to result from grazing. Though salinity divides the Bay into different biogeochemical provinces there is no relation between salinity and DMS or DMSPt. On the other hand DMS was linearly related to chlorophyll a:phaeopigments ratio. The results suggest the need for deeper insight into the role of diatoms in the biogeochemical cycling of DMS.  相似文献   

14.
Seasonal and spatial distributions of dissolved and particulate dimethylsulfoxide(DMSOd,DMSOp)were measured in the East China Sea and the Yellow Sea during March–April 2011 and October–November 2011.The concentrations of DMSOd and DMSOp in the surface water were 20.6(5.13–73.8)and 8.90(3.75–29.6)nmol/L in spring,and 13.4(4.17–42.7)and 8.18(3.44–22.6)nmol/L in autumn,respectively.Both DMSOd and DMSOp concentrations revealed similar seasonal changes with higher values occurring in spring,mainly because of the higher phytoplankton biomass observed in spring.Moreover,the ratios of DMSOp/chlorophyll a also exhibited an apparent seasonal change with higher values in autumn(35.7 mmol/g)and lower values in spring(23.4 mmol/g),thereby corresponding with the seasonal variation in the proportion of DMSO producers in the phytoplankton community between spring and autumn.In addition,DMSOd and DMSOp concentrations in the surface seawater revealed obvious diurnal variations with the maxima appearing in the afternoon.  相似文献   

15.
Dimethylsulfide (DMS) is a volatile sulfur compound produced by the marine biota. The flux of DMS to the atmosphere may act on climate via aerosol formation. It is therefore important to improve our understanding of the processes that regulate sea surface DMS concentrations for eventual inclusion into climate models. In order to simulate the dynamics of DMS concentrations in the mixed layer, a model of DMS production was developed and calibrated against a 1 year time-series of DMS and DMSP (dissolved and particulate) data collected in the Sargasso Sea at Hydrostation ‘S’. The model reproduces the observed divergence between the seasonal cycles of particulate DMSP, the DMS precursor produced by algae, and DMS produced through the microbial loop from the cleavage of dissolved DMSP. DMSPp (particulate) reaches its maximum in the spring whereas DMSPd (dissolved) and DMS reach maximum concentrations in summer. Several parameters had to vary seasonally and with depth in order to reproduce the data, pointing out the importance of physiological and structural changes in the plankton food web. These parameters include the intracellular S(DMSp):N ratio, the C:Chl ratio and the sinking rates of phytoplankton and detritus. For the Sargasso Sea, variations in the solar zenithal angle, which co-vary with the seasonal variations in the depth of the mixed layer, proved to be a convenient signal to drive the seasonal variation in the structure and dynamics of the plankton. Variations of the temperature and photosynthetically active radiation also help to reproduce the short-term variability of the annual S cycle. Results from a sensitivity analysis show that variations in DMSPp are dependent mostly on parameters controlling phytoplankton biomass, whereas DMS is dependent mostly on variables controlling phytoplankton productivity.  相似文献   

16.
The distribution and chemical properties of chromophoric dissolved organic matter (CDOM) in the Jiaozhou Bay, China were examined during four cruises in 2010-2011. The influence of freshwater and industrial and municipal sewage along the eastern coast of the bay was clearly evident as CDOM levels (defined as a 305 ), and dissolved organic carbon (DOC) concentrations were well correlated with salinity during all the cruises. Moreover, DOC concentrations were significantly correlated with chlorophyll a concentrations in the surface microlayer as well as in the subsurface water. The concentrations of DOC and CDOM displayed a gradually decreasing trend from the northwestern and eastern coast to the central bay, and the values and gradients of their concentrations on the eastern coast were generally higher than those on the western coast. In addition, CDOM and DOC levels were generally higher in the surface microlayer than in the subsurface water. In comparison with DOC, CDOM exhibited a greater extent of enrichment in the microlayer in each cruise, with average enrichment factor (E F ) values of 1.38 and 1.84, respectively. Four fluorescent components were identified from the surface microlayer and subsurface water samples and could be distinguished as peak A, peak T, peak B and peak M. For all the cruises, peak A levels were higher in the surface microlayer than in the subsurface water. This pattern of variation might be attributed to the terrestrial input.  相似文献   

17.
南黄海浮游植物季节性变化的数值模拟与影响因子分析   总被引：26，自引：1，他引：25  
用三维物理-生物耦合模式研究南黄海浮游植物(以叶绿素a为指标)的季节变化.对于物理模式采用Princeton ocean model(POM),对于生物模式考虑溶解无机营养盐(氮、磷、硅)、浮游植物、食草性浮游动物和碎屑.给定已知的初始场和外加边界强迫,模拟了观测到叶绿素a的主要时、空分布特征,如浮游植物的春、秋季水华和夏季次表层叶绿素a极大值现象等.研究表明,浮游植物春季水华最先发生于黄海中央海域,主要原因是该海域透明度较高,流速较小.春季水华开始于垂直对流减弱和层化开始形成之前(约3月底至4月上旬),显著地依赖水层的稳定性.水体层化以后(约5～9月)叶绿素a浓度高值区分布在南黄海的南部和锋区.夏季的南黄海中央海域,由于上混合层营养盐几乎耗尽,限制了浮游植物的生长,在紧贴温跃层下部的真光层,具有丰富的营养盐和合适的光照,次表层叶绿素a极大值得以形成.秋季(约9～11月份,略迟于海表面开始降温的时间,随地点不同而异)随垂直混合的增强,有利于营养盐向上输运,浮游植物出现一次较小的峰值.  相似文献   

18.
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   

19.
The coastal ecosystems are highly sensitive to climate change and are usually influenced by variations in phytoplankton communities and water physiochemical factors. In the present study, the phytoplankton community, chlorophyll a（Chl a） and their relationships with environmental variables and dimethylsulfide（DMS） and dimethylsulfoniopropionate（DMSP） were investigated in spring 2017（March 24 to April 16） in the East China Sea（26.0°–33.0°N, 120.0°–128.0°E） and southern Yellow Sea（31.0°–36.0°N, 12...  相似文献   

20.
dimethylsulphide (DMS)的海空通量是海洋生物气溶胶的主要来源之一,对气候（特别是北冰洋的气候）具有重要的辐射影响。利用卫星数据得到的气溶胶光学深度(AOD)作为气溶胶负荷的代表,在夏季和秋季表现的尤其明显。春季海冰的融化是北极气溶胶前体的重要来源。然而,早春的高浓度气溶胶可能与南方大陆污染的平流有关(北极霾)。更高的AOD通常在研究区域的南部出现。海冰浓度(SIC)和AOD呈正相关,而云盖(CLD)和AOD则呈负相关。SIC和CLD的季节性峰值均在AOD峰值的前一个月。AOD与SIC之间存在强烈的正相关关系。融冰与叶绿素（CHL)几乎在3月至9月呈正相关,但与春季和初夏的AOD呈负相关。春季和初夏较高的AOD有可能是由融冰和春季强风在该地区的结合影响。由于春季风的升高和冰的融化,在春季出现了DMS通量的峰值。从3月到五月,DMS浓度和AOD及融冰都呈正相关。早秋季升高的AOD可能与浮游植物合成的生物气溶胶的排放有关。到2100年,格陵兰海的DMS通量将增加3倍以上。生物气溶胶的显著增加可以部分抵消格陵兰海的增温现象。  相似文献   

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