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胶州湾双壳类壳体中的Ca,Mg,Mn,Sr元素组成及影响因素 总被引：1，自引：0，他引：1
探讨影响双壳类元素组成的可能因素,从胶州湾沿岸不同取样点采集黄海近海常见的菲律宾蛤仔(Ruditapesphilippinarum)、褶牡蛎(Oystrea denselamellosa)和紫贻贝(Mytilus galloprovincialis),分别测量了3种壳体的矿物物相类型和壳体中的Ca,Mg,Mn,Sr元素组成。研究表明:3种壳体分别属于文石质、方解石质和混合质壳;Ca,Mn元素含量在菲律宾蛤仔、褶牡蛎和紫贻贝壳体中没有差别,而Mg元素含量在菲律宾蛤仔壳体中含量较低,在褶牡蛎壳体和紫贻贝壳体中含量较高,Sr元素恰好与Mg元素相反。双壳类壳体中元素组成主要受壳体矿物物相类型的制约,而与水体环境要素之间的关系弱。 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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南海中部表层沉积物的元素地球化学 总被引：8，自引：0，他引：8
根据1983年9月—1984年7月所调查的南海中部91个表层沉积物中Fe,Mn等18种元素分析并结合其它资料的详细研究结果表明:(1)南海中部沉积物具有在近海—深海环境下形成的半深海沉积物的地球化学特征;(2)元素含量分布规律是,Al,K,Fe,Mg,Cu,Ce,Ni,Ba,Mn,Zn,Pb,N含量从陆架外缘到陆坡直至深海递增;Ca,Sr,C_(有机)从陆架外缘到陆坡含量渐增,由陆坡向深海锐减;Si和Ti含量在陆坡低、陆架外缘和深海高;(3)因子分析得出三种元素组合,即常量元素Al,Si,K,Fe,Mg,Ti,微量元素Cu,Co,Ni,Mn,Ba和Ca,Sr,C_(有机),N组合;(4)沉积物元素组成和含量的主要控制因素是沉积物类型。 相似文献
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生物地球化学在海洋地质方面的应用已引起人们的重视,尤其是用生物骨骼化学组成进行古环境解释已成为古海洋学研究的重要内容。本文对取自渤海西岸434m一钻孔中21个层位的45个介形虫壳体,利用扫描电镜和能谱仪分析了壳体的Ca,Mg,K,Mn,Ti,Al,Fe,Ba,Sr,Si和Ga‰11种元素成分含量,并进行了两次分析对照检验,其标准误差小于2‰。分析结果表明,介形虫壳的元素成分主要是Ca,平均含量83.86％,其次是Si(4.34％),Al(4.38％),Mg(2.71％),Fe(1.53％);K 相似文献
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碳酸盐生物壳体的周期性生长纹层是记录气候环境变化的天然材料。随着原位微区测试技术的快速发展,高分辨率的同位素和化学元素组成的快速分析显著推动了古气候环境变化及生物地球化学研究。应用激光剥蚀等离子体质谱仪(LAICP-MS)对南黄海现代牡蛎Crassostrea gigas壳体韧带部的元素组成进行原位微区测试,利用内标元素43Ca进行元素比值的校正,探讨了牡蛎壳中化学元素特征及其环境意义。研究的长牡蛎壳体中Mg/Ca、Sr/Ca、Na/Ca比值具有显著的季节性周期变化。环境水体物理化学性质的变化对壳体生长速率影响较大,壳中白垩质方解石和叶片方解石生长层分别对应较高和较低的环境温度,白垩方解石层具有较高的Mg/Ca、Sr/Ca和较低的Na/Ca比值。Mg/Ca比值可指示牡蛎壳体生长环境水体温度,利用前人Mg/Ca比值公式计算可以恢复与器测资料相符的近岸海水温度结果。本研究对应用LA-ICP-MS分析技术开展高分辨率的生物壳体元素组成和环境示踪研究具有借鉴意义。 相似文献
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《海洋地质与第四纪地质》2010,(3)
在210Pb同位素测年的基础上,通过对乌梁素海沉积物元素含量的分析,研究了沉积物中元素的变化规律,探讨了沉积物中元素变化的影响因素,结果表明沉积物中Ca、Sr、Cu、Mn、P等元素随深度加深含量下降,其余元素含量随深度加深呈增加的趋势。通过对元素富集系数的变化规律进行研究后,发现Ca、Sr、Cu、Mn、P等元素的富集系数与其含量变化趋势基本相同,反映了该组元素主要受沉积通量的影响;Al、K、Be、Ba、Mg等富集系数与其含量的变化趋势具明显差异,与黏土含量变化一致;而Cr、Fe、Ni、V、Co、Pb、Zn等重金属元素可能受到黏土吸附作用影响。最后,应用有序样品聚类分析方法,对元素这一环境代用指标在研究湖泊历史演化中的作用进行了探讨,研究表明:在湖泊演化过程中,湖泊的形成、20世纪70年代入湖水量的急剧改变以及近年来河套灌区化肥用量逐年加大、大量生活污水和工业废水排入等人类活动的增强等事件,均在湖泊沉积物元素的变化中有所体现。 相似文献
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本文测定了取自黄海南部和东海北部的某些表层沉积物主要元素的含量.根据主要元素的丰度、概率分布及其共生组合得到下列结果: 1.Al、Fe、Mg、Na、K的高含量分布地区与粘土沉积物相一致.Si的高含量区与砂质沉积相一致.Ca的高含量区与生物碎屑沉积物相一致; 2.Al与K、Mg、Na、Fe呈正相关.Mg与Fe之间,Si、P和Al之间也是正相关,Ca和Mn与Al没有明显的关系; 3.沉积物中Al、Fe、Mn、Mg、Na、K和P的含量随着远离海岸和海水深度增加趋于降低,Ca的变化没有规律。相反,在东海北部随着水深Ca含量增加,而Si与水深没有明显关系; 4.黄海沉积物来源于黄河,东海北部沉积物来自长江。 相似文献
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青岛近海秋末冬初悬浮颗粒物中部分金属元素的组成与影响因素研究 总被引：2，自引：0，他引：2
2008年11月末在青岛近海和胶州湾11个站点采集表层和底层海水中的悬浮颗粒物(SPM)样品,经消解后用等离子体发射光谱法测定了Al、Ca、Fe、Mg、Mn、Ti和Ba、Co、Cr、Cu、Ni、Pb、Sr、V、Zn共15个金属元素以及P的含量,结合SPM和元素含量聚类分析的结果探讨了秋末冬初青岛近海SPM的来源以及金属元素组成的影响因素.SPM含量范围在1.7～16.1mg/L之间,平均为7.9 mg/L;SPM来源以陆源风化产物为主,生物生产有较小的贡献.SPM中Ti、Fe、Mn、Mg、Al、V、Co、Sr和Ni的含量相对恒定,且主要受陆源输入的控制;Ca和P除受陆源影响外,生物生产亦有附加贡献.离陆地相对较远的区域表层海水SPM中Pb、Zn和Ba、Cr、Cu的含量较高,特别是Pb和Zn的富集因子较大,可能受到了潜在的污染影响.Ti的恒定性以及与SPM的良好相关性代表着在青岛近海可用Ti作为颗粒物陆源指示元素,且优于Al. 相似文献
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南海北部冷泉碳酸盐岩具有包裹结构和孔洞结构,并且含有丰富的生物遗迹。利用电子探针对位于不同结构单元(包裹结构和基质)的自生碳酸盐矿物和钙质生物壳体进行了Mg/Ca和Sr/Ca分析,结果显示:自生碳酸盐矿物Mg/Ca变化范围为0.50~39.19mmol/mol,平均为12.50mmol/mol,Sr/Ca变化范围为0.06~2.90mmol/mol,平均为0.53mmol/mol;钙质生物壳体Mg/Ca变化范围为1.14~84.57mmol/mol,平均为24.57mmol/mol,Sr/Ca变化范围为0.77~1.84mmol/mol,平均为1.08mmol/mol。Mg/Ca和Sr/Ca的关系显示自生碳酸盐矿物均具有低到中等的Mg/Ca、低Sr/Ca的特征,没有明显分组现象;但是钙质生物壳体却根据其在岩石中的结构位置呈现明显的分组现象,基质钙质生物壳体具有高Mg/Ca、中等Sr/Ca的特征,包裹的钙质生物壳体具有低Mg/Ca、中等Sr/Ca的特征。根据碳酸盐矿物和钙质生物壳体的Mg/Ca特征,认为基质钙质生物壳体是在甲烷渗漏环境下钙化的,无机碳酸盐矿物的出现影响了其Mg/Ca;而包裹的钙质生物壳体是在非甲烷渗漏环境下钙化的,由于生物扰动、灌洗等作用以包裹团块的形式保存在碳酸盐岩中。依据Sr/Ca在成岩过程中的变化特点推测最初形成的基质钙质生物壳体可能具有较现在高的Sr/Ca。研究结果在甲烷渗漏信息地球化学指标提取方面具有一定意义。 相似文献
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Soil-sized particulates have been collected on board ship by a mesh technique from the lower troposphere of the North, Equatorial and South Atlantic Ocean, northern and southern Indian Ocean, South and East China Sea and various coastal localities.Spectrographic analysis reveals that, on average, the particulates have concentrations of Mn, Ni, Co, Ga, Cr, V, Ba, and Sr which are of the same order of magnitude as those in average crustal material. In contrast, the average concentrations of Pb, Sn, and Zn are one order of magnitude higher than those in average crustal material.Within this “world-wide” average there are significant geographical variations in the distributions of Pb, Sn, and Zn which may be related to anthropogenic sources.On the basis of trace-element distributions lower tropospheric soil-sized marine particulates have been divided into four genetic components; local, zonal, inter-zonal, and global. The proportions of these components vary geographically, and each component may have both a natural and an anthropogenic fraction. 相似文献
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Tautog, Tautoga onitis, is an abundant species of fish in estuaries of the northeastern United States. Planktonic tautog larvae are abundant in summer in these estuaries, but there is little information on rates of growth of tautog larvae feeding on natural assemblages of food in the plankton. We examined abundance and growth of larval tautog and environmental factors during weekly sampling at three sites along a nearshore‐to‐offshore transect in Buzzards Bay, Massachusetts, USA during summer 1994. This is the first study of a robust sample size (336 larvae) to estimate growth rates of field‐caught planktonic tautog larvae feeding on natural diets, using the otolith daily‐growth‐increment method. The study was over the entire summer period when tautog larvae were in the plankton. The sampling sites contrasted in several environmental variables including temperature, dissolved oxygen (DO), and chlorophyll a concentration. There was a temporal progression in the abundance of tautog larvae over the summer, in relation to location and temperature. Tautog larvae were first present nearshore, with a pronounced peak in abundance occurring at the nearshore sites during the last 2 weeks in June. Larvae were absent at this time further offshore. From late June through August, larval abundance progressively decreased nearshore, but increased offshore although never approaching the abundance levels observed at the nearshore sites. The distribution and abundance of tautog larvae appeared to be related to a nearshore‐to‐offshore seasonal warming trend and a nearshore decrease in DO. Otoliths from 336 larvae ranging from 2.3 to 7.7 mm standard length had otolith increment counts ranging from 0 to 19 increments. Growth of larval tautog was estimated at 0.23 mm·day?1, and length of larvae prior to first increment formation was estimated at 2.8 mm indicating that first increment formation occurs 3–4 days after hatching at 2.2 mm. Despite spatial and temporal differences in environmental factors, there were no significant differences in growth rates at any of three given sites over time, or between sites. Because larval presence only occurred at a narrow range of temperature (17–23.5 °C) and DO (6.5–9.3 mg·l?1), in situ differences in growth did not appear to be because of differences in larval distribution and abundance patterns relative to these parameters. 相似文献
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Lars-Göran Danielsson 《Marine Chemistry》1980,8(3):199-215
Results of trace-metal analyses of water samples obtained during a cruise with the Soviet R.V. “Akademik Kurchatov” in the Indian Ocean are presented. The determinations were performed on board with atomic absorption spectrophotometry after a two-stage dithiocarbamate—Freon extraction procedure. Trace-metal concentrations found are in the same range as those found recently for similar open-ocean areas by other workers. The values for lead and zinc are probably high due to contamination. Vertical profiles indicate biogenic processes as controlling factors for the increase of cadmium, copper and nickel concentrations with depth. Iron shows an irregular depth distribution as a result of large random variations in concentration. 相似文献
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Klaus Kremling 《Marine Chemistry》1983,13(2):87-108
In June 1981, dissolved Zn, Cd, Cu, Ni, Co, Fe, and Mn were determined from two detailed profiles in anoxic Baltic waters (with extra data for Fe and Mn from August 1979). Dramatic changes across the O2H2S interface occur in the abundances of Cu, Co, Fe, and Mn (by factors of ?100). The concentrations of Zn, Cd, and Ni at the redox front decrease by factors between 3 to 5.Equilibrium calculations are presented for varying concentrations of hydrogen sulfide and compared with the field data. The study strongly supports the assumption that the solubility of Zn, Cd, Cu, and Ni is greatly enhanced and controlled by the formation of bisulfide and(or) polysulfide complexes. Differences between predicted and measured concentrations of these elements are mainly evident at lower ΣH2S concentrations.Cobalt proved to be very mobile in anoxic regions, and the results indicate that the concentrations are limited by CoS precipitation. The iron (Fe2+) and manganese (Mn2+) distribution in sulfide-containing waters is controlled by total flux from sediment-water interfaces rather than by equilibrium concentrations of their solid phases (FeS and MnCO3). The concentrations of these metals are therefore expected to increase with prolonged stagnation periods in the basin. 相似文献
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P.N. Froelich L.W. Kaul J.T. Byrd M.O. Andreae K.K. Roe 《Estuarine, Coastal and Shelf Science》1985,20(3):239-264
Concentrations of dissolved nutrients (NO3, PO4, Si), germanium species, arsenic species, tin, barium, dimethylsulfide and related parameters were measured along the salinity gradient in Charlotte Harbor. Phosphate enrichment from the phosphate industry on the Peace River promotes a productive diatom bloom near the river mouth where NO3 and Si are completely consumed. Inorganic germanium is completely depleted in this bloom by uptake into biogenic opal. The ratio taken up by diatoms is about 0·7 × 10?6, the same as that provided by the river flux, confirming that siliceous organisms incorporate germanium as an accidental trace replacement for silica. Monomethylgermanium and dimethylgermanium concentrations are undetectable in the Peace River, and increase linearly with increasing salinity to the seawater end of the bay, suggesting that these organogermanium species behave conservatively in estuaries, and are neither produced nor consumed during estuarine biogenic opal formation or dissolution. Inorganic arsenic displays slight removal in the bloom. Monomethylarsenic is produced both in the bloom and in mid-estuary, while dimethylarsenic is conservative in the bloom but produced in mid-estuary. The total production of methylarsenicals within the bay approximately balances the removal of inorganic arsenic, suggesting that most biological arsenic uptake in the estuary is biomethylated and released to the water column. Dimethylsulfide increases with increasing salinity in the estuary and shows evidence of removal, probably both by degassing and by microbial consumption. An input of DMS is observed in the central estuary. The behavior of total dissolvable tin shows no biological activity in the bloom or in mid-estuary, but does display a low-salinity input signal that parallels dissolved organic material, perhaps suggesting an association between tin and DOM. Barium displays dramatic input behavior at mid-salinities, probably due to slow release from clays deposited in the harbor after catastrophic phosphate slime spills into the Peace River. 相似文献