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利用电感耦合等离子质谱ICP-MS元素分析方法,测定了黄、渤海125尾小黄鱼的耳石元素指纹图谱,共检测到Mg、Al、Mn、Cu、Zn、Sr、Ba、Ca等8种指纹元素。不同采样站位小黄鱼耳石元素含量均存在显著性差异,线性判别分析可以有效识别不同站位的小黄鱼群体,判别成功率为65%~96%,整体判别成功率为86%。基于耳石元素指纹图谱特征进行聚类分析,可以将黄、渤海小黄鱼早期补充群体划分为渤海种群、黄海中部种群和南黄海种群,其中黄海中部种群站位交叉明显。  相似文献   

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构建了多测点激光剥蚀取样(LA)-ICPMS元素分析-剥蚀点显微结构验证的耳石核区元素指纹分析技术,以此进行了五个刀鲚群体(辽东湾、渤海湾、黄河口、胶州湾及长江口群体)识别的实证研究。结果发现,耳石核区Sr:Ca和Ba:Ca比值是有效识别各地理群体的元素指纹,基于二者的各群体判别成功率在46.2%—92.3%之间,总体...  相似文献   

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本文通过对山东莱州仓上泻湖Y86孔柱状样的系统取样,利用X荧光光谱分析了沉积柱状样品中的主要微量元素含量,结合已有的粒度分析、微体古生物及孢粉结果相分析对比,对泻湖沉积相进行地球化学判别,结果表明,Rb,Cr,Nb,Ni,Rb,Sr,Th,V,Zn,Zr等元素含量及Sr/Ba,Sr/Ca、Mn/Fe比值在不同的沉积相中均有明显的变异特征。因此可根据泻湖沉积物中的微量元素含量及Sr/Ba,Sr/Ca,Mn/Fe比值判别泻湖沉积环境及沉积相。  相似文献   

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东北太平洋中国合同区悬浮颗粒物元素地球化学   总被引:1,自引:0,他引:1  
利用ICP-MS对东北太平洋中国合同区3个测站分层采集的悬浮颗粒物的元素组成进行了测试,对Na、Mg、Al、Ca、Ti、Mn、Fe、Co、Cu、Sr、Ba和Pb等12种元素的含量分布及其地球化学特征进行了研究和对比。结果表明,水体中悬浮体总量(TSM)一般低于0.3mg/dm3,12种元素含量从几百到不足0.01μg/dm3。其分布以500和5000m为界可分为3层。元素中Al和Ti可作为陆源元素指标,Sr和Ba可作为生源元素指标,Pb主要来源于人类活动。在西区,Na、Mg和Ca主要为生源元素,Mn、Fe、Co和Cu主要为陆源元素。在东区,Na、Mg和Cu为多源元素,Ca、Mn、Fe和Co以陆源为主。颗粒物物源及供应量是颗粒物和元素含量分布的控制因素。西小区海底火山活动强烈是影响两区元素组分差异的直接因素之一。  相似文献   

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金岳  李楠  俞骏  方舟  陈新军 《海洋与湖沼》2021,52(6):1540-1548
根据2016年5月于南海北部采集的中国枪乌贼(Uroteuthis chinensis)和剑尖枪乌贼(U.edulis)样本,分析其不同时期耳石微量元素的差异,推测两种枪乌贼类可能的洄游路线。研究结果表明,选取的枪乌贼样本均孵化于2015年10月-2016年2月,其中主要分布于11-12月。中国枪乌贼耳石Sr/Ca随着月份推移呈现出先降低后回升的趋势;剑尖枪乌贼耳石Sr/Ca在不同月份间有更多的变化,稚鱼期的Sr/Ca为最低;中国枪乌贼耳石的Ba/Ca值随着生长而下降,成鱼期迅速上升,剑尖枪乌贼耳石Ba/Ca由仔鱼期后开始逐渐下降,至成鱼期逐步回升。根据耳石Ba/Ca与水深关系确定了不同生长时期对应的水层,随后将对应水层的平均温度与Sr/Ca建立关系,发现除1月孵化的中国枪乌贼外其耳石Sr/Ca与水温均呈正相关,而剑尖枪乌贼耳石Sr/Ca与水温均呈负相关。根据上述结果,最后推测两种枪乌贼的洄游方式均在大陆架范围内进行南北定向洄游。  相似文献   

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本研究以2015年和2017年我国远洋鱿钓渔船在东南太平洋的厄瓜多尔、秘鲁和智利公海生产时采集的茎柔鱼眼睛晶体为研究材料,采用LA-ICPMS测定了眼睛晶体外缘的微量元素,比较微量元素地理区域间差异,分析微量元素浓度与茎柔鱼栖息水温的关系。结果显示,厄瓜多尔、秘鲁和智利公海的茎柔鱼眼睛晶体外缘Mg25、Ni60 、Cu63、Sr88和Ba137等元素在3个海区之间存在显著差异(p<0.05),Na23、Al27、Si29、P31、Ca43、Mn55、Zn66和Pb等元素在两两海区之间均不存在显著差异(p>0.05)。除了Sr88、Ba137、Fe57和Ni60与海表面温度呈显著的线性负相关,其他元素与海表面温度均无显著的相关关系。分析认为,Sr88、Ba137、Fe57和Ni60均可以看作茎柔鱼生活水温的指示元素,Ba137元素还可以看作茎柔鱼生活水深以及上升流的指示元素。研究认为,眼睛晶体微量元素可用于头足类栖息环境的重建。  相似文献   

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本文对海南岛南岸三亚湾2008~2009年海水的周间隔取样,用全谱直读等离子体原子发射光谱(ICP-AES)分析方法对其Sr/Ca、Mg/Ca比值进行了测定。结果显示其比值(Sr/Ca=8.558~9.227mmol/mol,Mg/Ca=4.924~5.403 mol/mol)与全球各大洋和主要珊瑚礁区有明显地高异常偏差,而且在春末夏初和秋末冬初两个过渡期,三亚湾海水Sr/Ca比值波动幅度比Mg/Ca相对较大,且体现了一定的差异性。在此基础上,结合海水的Sr/Ca、Mg/Ca比值在时间和地域空间上的变化对珊瑚温度计标定的影响,及对不同站点建立的珊瑚Sr/Ca温度计进行了重新校正,并与分配系数法对比分析,我们认为利用珊瑚的Sr/Ca、Mg/Ca比值重建古SST记录时必须综合考虑包括海水微量元素比值变化在内的各种影响因素对温度计标定的干扰。  相似文献   

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经野外取样和地球化学测试分析,即墨温泉喷流沉积物呈现元素的富集并形成Fe,Ba,Li,La,Ce,Sc等10种元素的正异常.喷流沉积物中的Fe/Ti,(Fe Mn)/Ti及Al/(Al Fe Mn)比值分别为22.63,22.76和0.36~0.39,具有高铁低铝的热水沉积地球化学标识特征,符合Bostrom K.的热水沉积的标识;越流沉积物呈现诸多元素的亏损与负异常;越流沉积的Fe/Ti,(Fe Mn)/Ti及Al/(Al Fe Mn)比值仅为5.91,5.97和0.65,不具备热水沉积标识特征;通道-喷口沉积物呈现元素的富集并形成La,Ce,Sc,Sr元素的正异常.通道-喷口沉积中的Fe/Ti,(Fe Mn)/Ti及Al/(Al Fe Mn)比值分别为17.14,17.26和0.42,与>20,>20±5,<0.35比值比较,基本具备热水沉积特征,符合Bostrom K的热水沉积的标识.根据上述地球化学标识特征,结合温泉沉积的沉积学、矿物学标识,将即墨温泉沉积物划分为喷流相沉积、越流相沉积和通道-喷口亚相沉积并阐述其 "盆下源"沉积模式.  相似文献   

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东海陆架晚第四纪沉积物化学成分及物源示踪   总被引:11,自引:0,他引:11  
东海陆架EA1孔和EA5孔沉积物化学成分变化范围较大。与东海陆架表层沉积物相比,钻孔沉积物的Si,Al,Mg,Mn,Ti,P,Ba,Zr,Co,Ni,Cu,Zn,Cr明显偏高,而Fe,Na,Ca,Sr,Li,U明显偏低,与全球大陆地壳化学组成相比,钻孔沉积物的Si,Li,Rb,Ba,Th,Zr,Hf,Cu,Zn,Pb偏高,而Al,Na,Ca,Mg,Fe,Mn,Ti,P,Sr,U,Co,Ni,V,Cr偏低,钻孔沉积物的化学成分在垂向上具有明显变化,主要受岩性和沉积环境的控制,钻孔沉积物中元素的富集因子(EF)均小于10,接近于1,表明钻孔沉积物主要来自大陆地壳,一些元素因分异或外来物质加入而富集,一些元素则因分异带出而亏损,钻孔沉积物源区的DF值判别表明,钻孔沉积物与现代黄河,长江沉积物均有亲缘关系,可能是在末次冰期最盛期,由于气候带南移,干旱区域扩大,在古长江搬运沉积物中类似现今黄河沉积物的干旱组分明显增加,从而导致了地球化学示踪结果的长江与黄河双重性,或者说古气候的变化导致了古长江搬运物质成分的变化。  相似文献   

11.
The relationship between trace elements in chum salmon otoliths and in their rearing water was investigated to develop ways to distinguish chum salmon stocks in Korea. Rearing water and otoliths of hatchery-reared chum salmon fry were collected from three major hatcheries (Yangyang, Samchuk, and Uljin) on the east coast of Korea in spring 2001 and 2002. Trace elements in the otoliths and rearing water were analyzed using inductively coupled plasma mass spectrometry (ICP-MS) at the Korea Basic Science Institute. The chemical composition of rearing water and otoliths of the salmon fry at specific sites did not vary significantly through the study period. The ratios of some trace elements to Ca in rearing water, such as Sr/Ca and Ba/Ca, was clearly reflected in the chemical composition of otoliths, although the absolute concentrations were different. These two elements may be useful in distinguishing between salmon hatcheries, which have different chemical environments. Discriminant analysis with the ratios of eight elements to Ca (Na/Ca, Mg/Ca, Al/Ca, Cu/Ca, Sr/Ca, Ba/ Ca, Mn/Ca, and Zn/Ca) revealed a distinct separation of natal area in stocks. The analysis of otolith chemistry may be an effective technique for identifying the origins of wild salmon caught at sea.  相似文献   

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Fish growth and the relation between growth and environmental conditions offer a good opportunity for measuring alkaline and earthy ions in fish otoliths.The analytical method must involve high sensitivity when attempting to discriminate between fish growth and environmental conditions.The aim of this paper is to propose a chromatographic method, with low detection limits, as a new approach in determining some important micronutrients present in sea water and fish otoliths.The work samples are: coastal, off-shore and sediment waters and fish otoliths (Engraulis encrasicholus, Mullus barbatus, Umbrina cirrhosa, Sciaena umbra, Pagellus erythrinus) in the Adriatic Sea and the Canal of Sicily.The analytical method includes an IONPAC CS12A chromatographic column and a 18 mM methanesulfonic acid eluent.The detection limit readings obtained with this method, for one E. encrasicholus fish otolith, weighing 2.6 mg are equal or inferior to 0.1 μg/L for lithium (Li), 59 μg/L for sodium (Na), 46 μg/L for ammonium (NH4), 23 μg/L for potassium (K), 13 μg/L for magnesium (Mg), 88 μg/L for manganese (Mn), 2.567 μg/L for calcium (Ca) and 13 μg/L for strontium (Sr).The HPIC method minimizes overlaps such as Na on Li, and NH4 in seawater and Ca on Mg and Sr in fish otolith. These elements are an essential constituent present in otoliths when describing the relation between growth and environmental conditions.Good separation among analytes is achieved within 16 min.  相似文献   

14.
Chum salmon (Oncorhynchus keta) in the North Pacific Ocean are anadromous fish, and spend most of their life in the sea until spawning in natal streams. To identify the stock and habitat characteristics of chum salmon, the composition of chemical elements (Ca, Mn, Sr, Zn, and Ba) in otolith was examined using laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). Two main types of analytical work have been carried out; discrete spot analysis and line scan analysis of otolith sections. Salmon otoliths were obtained from the eastern (Canada and USA) and western (Japan and Korea) North Pacific during 1997–1999 spawning seasons. Spot analysis of otolith cores demonstrated significant differences in the element concentration among countries (p = 0.003). Line scanning from the core to the margin showed that Sr concentrations were elevated at the core of the otoliths, decreased during the freshwater stage, increased suddenly at a certain point, and oscillated periodically towards the margin matching with year-ring. The elevated Sr concentration at the core may reflect the maternal contribution to the egg, and the oscillations toward the margin may reflect salinity gradients between onshore/offshore or north/south migrations. The Zn profiles also oscillated and corresponded to the annual ring of the otolith. However, the profiles of Sr and Zn oscillated oppositely after salmon migrated to saline water and the Zn uptake declined toward the rim of the otolith while Sr uptake increased.  相似文献   

15.
We tested whether estuarine fishes have site-specific differences in the concentrations of trace elements in their otoliths that can be used as ‘fingerprints’ to identify them to their estuary of origin. To evaluate the robustness of this approach, we tested whether elemental fingerprints were consistent among individuals of five species that were collected in 1996 from three temperate estuaries in southern California. We also tested whether elemental fingerprints were consistent between spring and autumn 1996 for three species in one of the sites, Carpinteria Marsh. The species evaluated comprised a mid-water-dwelling smelt (Atherinops affinis), two benthic gobies (Clevelandia ios and Ilypnus gilberti), and two flatfish (Paralichthys californicus and Hypsopsetta guttulata). The concentrations of six elements (Mn, Cu, Zn, Sr, Ba, and Pb) were determined in the otoliths using inductively coupled plasma-mass spectrometry (ICP-MS). Within estuaries, the five species exhibited strong variation in elemental concentration, indicating substantial interspecific differences in otolith environmental history. When the five fish species were considered separately, multivariate (MANOVA) and univariate (ANOVA) analyses of variance indicated that the elemental composition of otoliths differed significantly among the estuaries in four of the five species. Based on linear discriminant function analyses (DFA), differences were strong enough that trace element composition could be used to accurately assign fish to their site of origin [mean (range): 93.5% (74–100%)]. However, elemental signatures within Carpinteria Marsh were not consistent between spring and autumn 1996, and this was reflected in a substantial reduction in the accuracy of assigning fish to their true site of origin. When we compared site differences between fish species (site×species interactions), the elemental fingerprints were most similar between closely related species (e.g. the two gobies and the two flatfish) and most dissimilar between distantly related species, both phylogenetically and ecologically. Among the six elements analyzed, Sr and Ba exhibited the most inconsistent pattern among species, with significant differences in 80 and 70% of the pairwise species comparisons, respectively. The remaining four elements showed ≥70% consistency in the pattern of variation among sites for the different species. Thus, while otolith elemental fingerprinting can be a useful tool for inferring estuarine residency, such fingerprints may be temporally variable and species specific.  相似文献   

16.
长江口水域四种鱼类的耳石微化学研究   总被引:2,自引:0,他引:2  
刘洪波  姜涛  邱晨  杨健 《海洋与湖沼》2018,49(6):1358-1364
利用X-射线电子探针微区技术(electron probe microanalysis, EPMA),对长江口不同水域中捕获的焦氏舌鳎、皮氏叫姑鱼、鮸鱼和光泽黄颡鱼耳石中的Sr含量进行耳石微化学研究,结果发现,焦氏舌鳎是典型的海水鱼类,不仅Sr:Ca比(按惯例标准化为Sr:Ca×10~3)的移动平均值高(7),而且Sr含量面分析图亦呈现为对应高盐度海水的黄色或红色图谱。虽然皮氏叫姑鱼和鮸鱼从出生直至被捕Sr:Ca比的移动平均值都在3—7间波动,总体上属河口半咸水栖息鱼类,但从Sr含量面分析图来看,皮氏叫姑鱼生活史履历更为复杂,可包括淡水(对应蓝色图谱)和半咸水生境(对应绿色图谱);而鮸鱼仅在长江口较高盐度半咸水或海水生境中活动,未见进入过淡水的履历。光泽黄颡鱼表现出仅利用淡水生境的履历,其Sr:Ca比的移动平均值仅在1.5—3间窄幅波动,整个生活史均在淡水区域里活动,表现为长江口典型的淡水栖息鱼类。本研究从新的角度提供了较为客观、直观和最新的信息,用以较为准确地重建和掌握长江口这些不同鱼类的生境利用特征。  相似文献   

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Habitat use of the tapertail anchovy(Coilia mystus Linnaeus, 1758) from the Oujiang River Estuary and the Zhujiang(Pearl) River Estuary was studied by examining the environmental signatures of Sr and Ca in otoliths using electron probe microanalysis. Individuals from the Oujiang River had higher and varied Sr:Ca ratios(expressed as(Sr:Ca)×1 000, 3.83–13.0 average) in the otolith core regions, suggesting that they were born in brackish or sea waters, and that a freshwater habitat might not be necessary for egg hatching and larval growth.While, individuals from the Zhujiang River had lower Sr:Ca ratios(0.39–2.51 average) in the core regions,suggesting a freshwater origin. After hatching, anchovies from the Zhujiang River migrate downstream to the river estuary close to brackish water. Our results demonstrated varied habitat use for spawning during stages of early life history between the two populations, and suggested that such variations are promoting diversity of life history strategies of this species.  相似文献   

18.
Estuaries are dynamic environments in which chemical properties can vary over small time-scales. Chemical properties of water are reflected in calcified structures of organisms, such as fish otoliths (ear bones). Interpretations of otolith chemistry can be enhanced using information on the temporal stability of ambient chemistry. We assessed temporal variation in temperature, salinity (environmental variables), and elemental concentrations of strontium (Sr), calcium (Ca), barium (Ba), and manganese (Mn), within three estuarine or coastal locations. Temporal variation was assessed over a series of nested temporal scales: seasons, months, weeks, days, and tidal cycles. Variation in elemental concentration was found between seasons, weeks, and days for the majority of elements, but not between months. Differences in Sr, Ca, Ba, and Mn were found over tidal cycles (low versus high tide) in one estuary. The results provide a clear demonstration that samples collected over a range of temporal scales can detect small-scale variability in water chemistry, the magnitude of which can equal or exceed variability over larger temporal scales. Thus, we stress caution in inferring environmental histories from chemicals in calcified structures within dynamic estuarine environments, when small-scale temporal variability is large.  相似文献   

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