氯甲烷的海洋生物地球化学研究     

陆小兰  杨桂朋  高先池 《中国海洋大学学报(自然科学版)》2006,36(6):868-874

对氯甲烷的海洋生物地球化学循环的研究进展进行述评。介绍了氯甲烷在海洋环境中的来源、分布、去除、海-气通量、大气氯甲烷的源、汇估算及海水中氯甲烷的分析方法等方面,并提出在国内海域进行氯甲烷研究的几点设想。  相似文献   

Tidal fluxes of nutrients and suspended sediments at the North Inlet–Winyah Bay National Estuarine Research Reserve     

L.R. Gardner  B. Kjerfve   《Estuarine, Coastal and Shelf Science》2006,70(4):682

Beginning June of 1993 suites of 13 water samples have been collected at Oyster Landing, North Inlet (SC), every 20 days covering two consecutive tidal cycles at 2.07 h intervals. In order to ascertain whether this large (and still growing) water chemistry data set can be used to determine tidal fluxes of nutrients and sediments, we coupled measured concentrations to estimates of instantaneous tidal discharge based on a basin water storage curve and hindcast tides. The mean advective fluxes of all constituents, including salt, showed statistically significant exports. This result, however, is largely due to an ebb bias in the sampling protocol, which resulted in 52% of the samples being collected on ebb tide versus a theoretical percentage of 48%. When this bias was corrected by reducing the mean discharge (−610 l s⁻¹) to a value (−125 l s⁻¹) that produced a balance between the mean advective and dispersive salt fluxes, the advective fluxes of the other constituents were reduced to values that are not significantly different from zero. In addition to a statistically significant dispersive influx of salt, significant dispersive exports were found for DON, NH₄, DOP, PO₄ and DOC. All particulate constituents (PN, PP, ISS and OSS) yielded dispersive fluxes that were not significantly different from zero. Annual material budgets for the Oyster Landing basin based on the dispersive fluxes of all constituents (except salt) are generally similar in magnitude and direction to those measured by [Dame, R.F., Spurrier, J.D., Williams, T.M., Kjerfve, B., Zingmark, R.G., Wolaver, T.G., Chrzanowski, T.H., McKeller, H.N., Vernberg, F.J., 1991. Annual material processing by a salt marsh-estuarine basin in South Carolina, USA. Marine Ecology Progress Series 72, 153–166.] in the nearby and ecologically similar Bly Creek basin, indicating that the dispersive fluxes determined in this study are realistic. We offer suggestions for improving the reliability and usefulness of future Oyster Landing water quality data.  相似文献   

Organic enrichment and structure of the macrozoobenthic community in the northern Adriatic Sea in an area facing Adige and Po mouths   总被引：1，自引：0，他引：1  

Simonini  R.; Ansaloni  I.; Bonvicini Pagliai  A.M.; Prevedelli  D. 《ICES Journal of Marine Science》2004,61(6):871-881

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现场海水中有机污染物光学测量方法研究     

孙继昌  惠力  吴承璇  程岩  程广欣  徐珊珊  宋文杰 《海洋技术学报》2005,24(4):54-56

介绍了一种用光学方法对海水中的有机污染物（主要包括：叶绿素-a、黄色物质、石油）进行测量的光学系统，该系统可同时测量海水中多种有机污染物的种类和浓度。  相似文献   

Effect of marine animal excretions on differential growth of phytoplankton species   总被引：2，自引：0，他引：2  

Arzul  Genevieve; Seguel  Miriam; Clement  Alejandro 《ICES Journal of Marine Science》2001,58(2):386-390

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High-resolution measurements of chromophoric dissolved organic matter in the Mississippi and Atchafalaya River plume regions   总被引：4，自引：0，他引：4  

Robert F. Chen  G. Bernard Gardner 《Marine Chemistry》2004,89(1-4):103

Chromophoric dissolved organic matter (CDOM) was measured in the spring and summer in the northern Gulf of Mexico with the ECOShuttle, a towed, instrumented, undulating vehicle. A submersible pump mounted on the vehicle supplied continuously flowing, uncontaminated seawater to online instruments in the shipboard laboratory and allowed discrete samples to be taken for further analysis. CDOM in the northern Gulf of Mexico was dominated by freshwater inputs from the Mississippi River through the Birdfoot region and to the west by discharge from the Atchafalaya River. CDOM was more extensively dispersed in the high-flow period in the spring but in both time periods was limited by stratification to the upper 12 m or so. Thin, subsurface CDOM maxima were observed below the plume during the highly stratified summer period but were absent in the spring. However, there was evidence of significant in situ biological production of CDOM in both seasons.The Mississippi River freshwater end member was similar in spring and summer, while the Atchafalaya end member was significantly higher in the spring. In both time periods, the Atchafalaya was significantly higher in CDOM and dissolved organic carbon (DOC) than the Mississippi presumably due to local production and exchange within the coastal wetlands along the lower Atchafalaya which are absent along the lower Mississippi. Nearshore waters may also have higher CDOM due to outwelling from coastal wetlands. High-resolution measurements allow the differentiation of various water masses and are indicative of rapidly varying (days to weeks) source waters. Highly dynamic but conservative mixing between various freshwater and marine end members apparently dominates CDOM distributions in the area with significant in situ biological inputs (bacterial degradation of phytoplankton detritus), evidence of flocculation, and minor photobleaching effects also observed. It is clear that high-resolution measurements and adaptive sampling strategies allow a more detailed examination of the processes that control CDOM distributions in river-dominated systems.  相似文献   

A Stable Carbon Isotope Study of the Food-web in a Freshwater-deprived South African Estuary, with Particular Emphasis on the Ichthyofauna   总被引：1，自引：0，他引：1  

A.W. Paterson  A.K. Whitfield 《Estuarine, Coastal and Shelf Science》1997,45(6):705-715

The importance of macrophytes as food sources for estuarine nekton is unclear. Previous carbon isotope investigations in the macrophyte-dominated, freshwater-deprived Kariega Estuary showed that the bivalveSolen cylindraceusdid not utilize the dominant estuarine macrophytes found within the estuary as a primary food source. This finding prompted questions as to what the nekton of this estuary utilize as primary energy sources. δ¹³C analyses of the principal autochthonous and allochthonous primary carbon sources, as well as the dominant invertebrate and fish species, indicate that there are two main carbon pathways within the Kariega Estuary. The littoral community, which incorporates the majority of crustaceans, gobies, mullet and a sparid, utilizes δ¹³C enriched primary food sources namelySpartina maritima,Zosteracapensis and epiphytes. The channel fauna, which includes the zooplankton, zooplanktivorous and piscivorous fish, utilizes a primary food source depleted in δ¹³C, which is most likely a mixture of phytoplankton, terrestrial plant debris and C₄macrophyte detritus. The C₃saltmarsh macrophytesSarcocornia perennisandChenolea diffusa, as well as benthic microalgae, appear to be less important as primary food sources to the nekton of the Kariega Estuary.  相似文献   

Environmental characteristics of the Mandovi-Zuari estuarine system in Goa   总被引：1，自引：0，他引：1  

S.Z. Qasim  R. Sen Gupta 《Estuarine, Coastal and Shelf Science》1981,13(5):557-578

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Geographic variability in trace element levels in Spartina alterniflora     

J.E. Drifmeyer  B. Redd 《Estuarine, Coastal and Shelf Science》1981,13(6):709-716

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Seasonal methyltin and (3-dimethylsulphonio)propionate concentrations in leaf tissue of Spartina alterniflora of the Great Bay estuary (NH)     

James H. Weber  Marilyn R. Billings  Anne M. Falke 《Estuarine, Coastal and Shelf Science》1991,33(6)

Concentrations of total recoverable inorganic tin (TRISn), monomethyltin (MeSn³⁺), dimethyltin (Me₂Sn²⁺), trimethyltin (Me₃Sn⁺) and (3-dimethylsulphonio)propionate (DMSP) were determined in leaves of Spartina alterniflora from three sites in the Great Bay estuary (NH) from 8 May to 15 September 1989. Total methyltin concentration increased from 8·9 ng g⁻¹ (fresh weight) on 8 May to 472 ng g⁻¹ on 23 May, decreased to 52 ng g⁻¹ on 7 June and 16ng g⁻¹ on 20 June, and remained low until the last sample on 18 September. Statistical calculations showed that methyltin concentrations varied significantly with sampling week, but not with site. DMSP concentrations showed very different behaviour. During the same sampling period DMSP concentrations varied only from 7·5 to 26 μmol g⁻¹ (fresh weight). DMSP concentrations varied significantly for site, but not sampling week.  相似文献