Assessment of spatial variation in carbon utilization by benthic and pelagic invertebrates in a temperate South African estuary using stable isotope signatures     

Nicole B. Richoux  P. William Froneman 《Estuarine, Coastal and Shelf Science》2007,71(3-4):545-558

Stable isotope analyses (δ¹³C and δ¹⁵N) were used to evaluate the spatial variations in carbon flow from primary producers to consumers at two sites in the temperate and permanently open Kariega Estuary on the southeastern coast of South Africa during October 2005 and February 2006. One site was located opposite a salt marsh while the second was upstream of the marsh. Except for significantly enriched δ¹³C values of Zostera capensis and surface sediments near the salt marsh, the δ¹³C and δ¹⁵N signatures of the producers were similar between sites. The invertebrates were clustered into groups roughly corresponding to the predominant feeding modes. The suspension feeders showed δ¹³C values closest to the seston, whereas the deposit feeders, detritivores and scavengers/predators had more enriched δ¹³C values reflecting primary carbon sources that were likely a combination of seston, Spartina maritima and Z. capensis at the upstream site, with an increased influence of benthic algae and Z. capensis at the salt marsh site. The δ¹⁵N signatures of the consumers showed a stepwise continuum rather than distinct levels of fractionation, indicating highly complex trophic linkages and significant dietary overlap among the species. Consumers exhibited significantly enriched δ¹³C values at the salt marsh site, an effect that was attributed to enriched Z. capensis detritus in this region in addition to increased phytoplankton biomass in their diets compared with invertebrates living upstream. The data reinforce the concept that between-site variations in the stable isotope ratios of consumers can result not only from dietary shifts, but also from alterations in the isotope ratios of primary producers.  相似文献   

九龙江河口区表层水铀同位素的粒级分布          下载免费PDF全文

吕娥  张磊  陈敏  邱雨生  邢娜  杨伟锋  李艳平  黄奕普 《海洋学报》2007,29(4):59-68

利用微滤和超滤技术研究了九龙江河口区表层水中铀及其同位素组成的粒级分布和地球化学行为.结果表明,溶解态(<0.4μm)中低分子量组分(<10 000 u)占主要份额,胶体态(10 000 u~0.4μm)238U所占比例不足1%,且随盐度的增加其所占份额逐渐降低.溶解态、低分子量组分和胶体态238U的比活度与盐度之间存在良好的线性正相关关系,证实它们在九龙江河口区呈现保守行为.在颗粒态(>0.4μm)中,各粒级组分238U所占份额主要受控于相应颗粒物的浓度,在盐度小于20的区域,各粒级颗粒组分238U占颗粒态的份额有如下变化次序:10~53μm>2~10μm>0.4~2μm>大于53μm,而在盐度大于30的近外海站位,该次序发生一些变化:0.4~2μm>10~53μm>2~10μm>大于53μm,最小粒级颗粒组分238U的贡献有所增加,反映了自生铀贡献的加强.九龙江河口区表层水中溶解态(包括低分子量组分和胶体态)的234U/238U)_A.R.均大于1,显示出234U过剩的特征,而各粒级颗粒组分中的234U/238U)_A.R.则接近于平衡值(1.0).这一现象与陆地岩石风化过程中水体对铀的淋滤释出量及234U的优先浸出有关.对232Th/238U质量比的研究显示,溶解态及其所包括的低分子量组分和胶体态的232Th/238U质量比均小于1,而颗粒态及其所包括的4个粒级组分中的232Th/238U质量比均大于1,反映了向外海输送过程中铀、钍地球化学行为的差异.  相似文献   

Determination of phospholipid fatty acid structures and stable carbon isotope compositions of deep-sea sediments of the Northwest Pacific, ODP site 1179   总被引：1，自引：0，他引：1  

Christopher T. Mills  Robert F. Dias  Dennis Graham  Kevin W. Mandernack   《Marine Chemistry》2006,98(2-4):197-209

Sediment samples ranging from 0.05 to 278 m below sea floor (mbsf) at a Northwest Pacific deep-water (5564 mbsl) site (ODP Leg 191, Site 1179) were analyzed for phospholipid fatty acids (PLFAs). Total PLFA concentrations decreased by a factor of three over the first meter of sediment and then decreased at a slower rate to approximately 30 mbsf. The sharp decrease over the first meter corresponds to the depth of nitrate and Mn(IV) reduction as indicated by pore water chemistry. PLFA-based cell numbers at site 1179 had a similar depth profile as that for Acridine orange direct cell counts previously made on ODP site 1149 sediments which have a similar water depth and lithology. The mole percentage of straight chain saturated PLFAs increases with depth, with a large shift between the 0.95 and 3.95 mbsf samples. PLFA stable carbon isotope ratios were determined for sediments from 0.05 to 4.53 mbsf and showed a general trend toward more depleted δ¹³C values with depth. Both of these observations may indicate a shift in the bacterial community with depth across the different redox zones inferred from pore water chemistry data. The PLFA 10me16:0, which has been attributed to the bacterial genera Desulfobacter in many marine sediments, showed the greatest isotopic depletion, decreasing from − 20 to − 35‰ over the first meter of sediment. Pore water chemistry suggested that sulfate reduction was absent or minimal over this same sediment interval. However, 10me16:0 has been shown to be produced by recently discovered anaerobic ammonium oxidizing (anammox) bacteria which are known chemoautotrophs. The increasing depletion in δ¹³C of 10me16:0 with the unusually lower concentration of ammonium and linear decrease of nitrate concentration is consistent with a scenario of anammox bacteria mediating the oxidation of ammonium via nitrite, an intermediate of nitrate reduction.  相似文献   

Differences in ratios of stable isotopes of nitrogen in long-finned pilot whales (Globicephala melas) in the western and eastern North Atlantic   总被引：1，自引：0，他引：1  

Abend  Alan G.; Smith  Tim D. 《ICES Journal of Marine Science》1995,52(5):837-841

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麻醉剂丁香酚对黄腊鯵耗氧的影响   总被引：20，自引：1，他引：20       下载免费PDF全文

张朝晖  丛娇日  王波  洪旭光  KjellφMidling 《海洋科学》2003,27(6):11-14

用不同浓度的丁香酚对体质量为 115～ 175 g的黄腊鲹( Trachinotus blochii)麻醉处理 15 min,每 1分钟测定容器内的氧饱和度 1次.实验结果表明,黄腊鲹的耗氧率明显地受到丁香酚的影响,在各处理组中以 10× 10- 6浓度组的耗氧率为最低( 0.33 mg/(g@ h)), 5× 10- 6浓度组次之( 0.42 mg/(g@ h)),而对照组则较高( 0.57 mg/(g@ h)).同时实验还表明经丁香酚麻醉处理的黄腊鲹鳃活动频率显著地比对照组低.此结果表明了在施用麻醉剂以后,鱼体的活动及对氧气的消耗有明显的下降,丁香酚可以作为活鱼运输过程中有效的麻醉剂.  相似文献   

Geochemistry of trace elements and Sr-Nd isotopes of foraminifera shell from the Okinawa Trough   总被引：1，自引：0，他引：1  

Meng Xianwei  Du Dewen  Cheng Zhenbo 《海洋学报(英文版)》2001,20(1):95-103

ＩＮＴＲＯＤＵＣＴＩＯＮＰｒｏｖｅｎａｎｃｅｏｆｍａｒｉｎｅｓｅｄｉｍｅｎｔｓｈａｓａｌｗａｙｓｂｅｅｎａｆｏｃｕｓｅｄｐｒｏｂｌｅｍｉｎｍａｒｉｎｅｓｅｄｉｍｅｎｔｇｅ ｏｌｏｇｙ.Ｒｅｃｏｇｎｉｔｉｏｎｏｆｅｎｄｍｅｍｂｅｒｓａｎｄｅｓｔｉｍａｔｉｏｎｏｆｔｈｅｉｒｒｅｌａｔｉｖｅｐｒｏｐｏｒｔｉｏｎｓｆｒｏｍｍｉｘｅｄｓｅｄｉｍｅｎｔｓｈａｖｅｂｅｅｎａｋｅｙｃｏｎｔｅｎｔｉｎｔｈｅｓｔｕｄｙｏｆｐｒｏｖｅｎａｎｃｅ .Ｆｏｒｔｈｉｓａｉｍ ,ｉｔｉｓｎｅｃｅｓｓａｒｙｔｏｓｅｌｅｃｔｅｎｄｍｅ…  相似文献   

Carbon stable isotopes in estuarine sediments and their utility as migration markers for nursery studies in the Firth of Forth and Forth Estuary, Scotland   总被引：2，自引：0，他引：2  

Julian Augley  Mark Huxham  Teresa F. Fernandes  Alastair R. Lyndon  Sarah Bury 《Estuarine, Coastal and Shelf Science》2007,72(4):648-656

The stable carbon isotope ratios (δ¹³C) of the organic fraction of intertidal sediments in the Forth Estuary and the Firth of Forth, Scotland, were measured to determine if terrestrially derived carbon was present in the estuarine sediments. It was hypothesised that differences in the inputs from marine vs. terrestrial sources to the organic carbon of estuarine and marine sediments, as well as differences in ambient seawater stable oxygen isotope (δ¹⁸O) ratios between the estuary and the Outer Firth, would allow the use of these two stable isotopes as habitat markers for juvenile plaice (Pleuronectes platessa), to allow determination of nursery habitats. Muddy and sandy sediments from the estuary and sandy sediments from the Outer Firth were sampled and δ¹³C measured. Juvenile plaice were caught at two estuarine sites and at two Outer Firth sites and otoliths were removed for δ¹³C and δ¹⁸O analysis. The sandy sediments in the estuary showed a strong gradient of δ¹³C enrichment with distance down the estuary, while the muddy sediments showed a much shallower gradient. δ¹³C and δ¹⁸O measured in the carbonate of juvenile plaice otoliths showed no clear difference between otoliths of fish caught at one of the estuarine sites and at the two Outer Firth sites. However, the isotope ratios of both carbon and oxygen in plaice otoliths from the other estuarine site showed the expected trend of depletion in the heavier isotopes. While the measurements recorded here did not conclusively distinguish between otoliths from juveniles caught in the estuarine site and those caught in the other three sites, they show that stable isotopes have potential to distinguish between estuarine habitats with terrestrial carbon inputs, and coastal marine habitats with predominantly marine carbon inputs.  相似文献   

Factors influencing the oxidation,reduction, methylation and demethylation of mercury species in coastal waters     

Lindsay Whalin  Eun-Hee Kim  Robert Mason 《Marine Chemistry》2007

The objective of this study was to examine the redox reactions and other transformations of mercury (Hg) species in surface waters, and the factors determining the rates of these reactions. For the redox studies completed at the Chesapeake Biological Laboratory (CBL), two isotopes (¹⁹⁹Hg^II and ²⁰²Hg⁰) were added into different types of filtered water (fresh to seawater) to examine the oxidation and reduction reactions. Further studies of both the redox reactions and methylation/demethylation reactions of Hg were conducted with unfiltered water on board research vessels during cruises in May and July 2005 on the Chesapeake Bay and shelf. While CH₃¹⁹⁹Hg^II was added to allow the examination of demethylation, ²⁰¹Hg^II was used to examine both reduction and methylation, and ²⁰²Hg⁰ was used to examine oxidation. Overall, the results showed that both Hg oxidation and reduction were simultaneously occurring and were photochemically mediated in the waters investigated. In contrast to the previously assumed “unreactive” nature of Hg⁰, the studies found that the magnitude of the rate constant for Hg⁰ oxidation was greater than that for reduction, indicating its importance in estuarine and coastal waters. In addition, both experiments at CBL and on board ship showed that Hg^II reduction was similar in magnitude, suggesting that biotic processes were relatively unimportant. While no measurable methylation occurred during the incubation period during the on board studies, concentration of CH₃¹⁹⁹Hg^II decreased over the time during the experiments. It appeared that the demethylation processes were not dominantly photochemically driven, but could be microbially mediated. Further studies are needed in order to help better understand Hg redox and transformations in natural water systems.  相似文献   

稳定同位素在天然气水合物地球化学勘查中的应用简介--以"布莱克海隆"海区为例   总被引：2，自引：0，他引：2  

陆尊礼  凌洪飞  蒋少涌  杨竞红  倪培 《海洋地质前沿》2003,19(2):28-32

介绍了国外在布莱克海隆（包括ODP164航次994、995、997站位）进行天然气水合物勘查过程中应用稳定同位素的研究实例；通过对这3个站位样品的甲烷、CO2、DIC（dissolved inorganic carbon)、有机碳以及自生碳酸盐的δ^13C分析，指出浅部（0－30m)甲烷和DIC的δ^13C值随深度迅速降低又迅速升高的变化可以作为天然气水合物存在的地球化学指标。994站位孔隙水δ^18O值深度从0.30‰下降到-0.37‰；氢同位素δD随深度略有下降（从11‰到-12‰），这与水合物形成时氢氧重同位素相对富集于固相有关，表明天然气水合物的存在。997站位δ^37Cl从海底沉积物表层以下30m处为接近海水的最大值0，至钻孔底746.85m处降为-3.68‰，可能也与天然气水合物的形成有关。  相似文献   

江苏海域水环境要素分析——江苏海域环境质量分析之二   总被引：3，自引：0，他引：3       下载免费PDF全文

丁贤荣  张鹰 《海洋科学》2003,27(2):8-12

在1981、1991（1990）和1998年3次海洋环境调查的基础上，通过相同水质要素时空比较分析，江苏海域的溶解氧、磷酸盐、硝酸盐和亚硝酸 盐这4种主要海水化学因子具有时空变化特征，其高值区主要分布在灌河口、扁担港口、射阳河口、川东港和长江北支口北侧，且河口、近岸值高，向海含量渐小，不同年份、季节也有变化。沿海水化学性质主要受陆源排污（农田化肥等）影响，主要是入海河流携带污染物、海洋生物作用和本海域水体运动特征的影响，此外，溶解氧变化还受到水温变化的影响。  相似文献