标志沉积层磁组构特征及其古环境意义研究

通过对长江三角洲及其邻近区域埋藏古土壤、潮坪、长江下游河道浸滩、舟山滨岸风成沙丘、南京黄土古土壤序列沉积体的磁组构测量统计分析，取得了各自的标志特征。该２特征揭示出，舟山滨岸风成沙丘与南京黄土吉土壤序列沉积的搬运介质能量位相基本一致，其物源来向却显示出巨大差异；上述两类沉积体与上述现今潮坪、河道漫滩沉积体地搬运介质能量位相及物源来向均显示出绝然不同的标志特征。然而浸滩物源来民南京黄土的物尖兵为向却     

大别山地区石榴石橄榄岩的岩石学和地球化学

本文首次对我国石榴石橄榄岩类岩石进行系统的岩石学和地球化学研究。通过对大别山地区两个不同类型岩体中的石榴石橄榄岩的岩石学、岩石化学、矿物化学和稀土元素地球化学研究,表明这类岩石属钙碱性系列超基性岩;与地幔成分相比,富集易熔元素,亏损难熔元素;利用矿物地质温压计估算其形成压力为2×10~9pa,成岩温度为600～700℃具有正铕异常和轻稀土元素富集特征 推测为地壳下部的超基性岩经深成变质而成。     

顶空气相色谱法测定海水二甲基硫和浮游植物细胞二甲基硫丙酸的研究

建立了顶空ＧＣ／ＦＰＤ测定海水中二甲基硫（ＤＭＳ）和浮游植物细胞中二甲基硫丙酸（ＤＭＳＰ）的方法，并研究盐度、温度、气液相比ＤＭＳ诸因素对ＤＭＳ顶空灵敏度的影响。该法对ＤＭＳ测定的相对标准偏差均小于６％，平均回收率为１０６％，最低检出限为２０ｎｇ／Ｌ。细胞ＤＭＳＰ先经碱作用转化为ＤＭＳ，在５０℃下作用时间不少于６ｈ，峰高与浓度的双对数线性相关系数大于０．９９。对１９９４年冬、１９９５年夏采自胶州湾     

南海尖峰海山多金属结壳地球化学

南海尖峰海山多金属结壳富含30多种元素,其锰铁矿物主要由钡镁锰矿,δ-MnO_2和FeOOH·xH_2O组成。与其它海区的结壳相比,尖峰海山结壳富含Cu、Ni、Ba、Zn、Pb等元素,而Co、Ti、稀土元素(REE)、Sr等元素相对较贫。研究表明,HREE亏损,具明显的Ce正异常,较明显的Tb正异常和Yb负异常。这是氧化弱碱性海洋环境所致。结壳是水成作用的产物,它的形成受南海独特的古海洋环境所控制,海底火山热液作用,可能也是影响因素之一。     

珠江口外陆架表层沉积物的地球化学分区

根据249个表层沉积物样品的Ca,Al,N,P,Mg,Fe,Mn,Ti和有机碳的测定数据,利用稳健RQ型主分量分析及Q型聚类分析方法,对珠江口外陆架表层沉积物进行了地球化学分类,并将该陆架区划分成陆源细碎屑沉积区、经叠加改造的残留泥砂质沉积区、生物碎屑沉积区以及高能环境下的石英砂质沉积区。结果表明了稳健统计方法相对于传统统计方法的优越性,以及采用稳健主分量的Q载荷进行聚类分析相对于用原始变量进行聚类分析的优越性。     

湄洲湾表层沉积物中重金属的地球化学特征

根据1984年湄洲湾表层沉积物中重金属的分析资料,讨论了它们的地球化学特征和主要来源。沉积物中重金属的含量(Fe、Mn、Cu、Ni 的质量分数均值分别为3.21%、730×10~(-6)、19.4×10~(-6)、44×10~(-6)分布比较均匀,Pb、Zn 和Co 含量(质量分数均值分别为47.0×10~(-6)、25.8×10~(-6)和243×10~(-6))偏高,微量金属含量不受Fe-Mn 氧化物和有机物控制,本地区的金属来源受陆源输入的影响明显。     

湄州湾沉积物地球化学特征

根据湄州湾表层沉积物70个样品18个化学成分的分析结果,得出:本海区沉积物属于海相陆源物,其中细颗粒主要来自台湾海峡,粗颗粒来自当地陆域;化学成分含量按聚类分析,可归为三组:粘土矿物组、碳酸盐组和分散组,微量元素Zn,Cr,Be,Cu和Sr的含量与地壳及台湾海峡相似,但低于胶州湾,说明该海区污染很少。     

鲁苏榴辉岩的地球化学

以微量元素、稀土元素、Ｓｒ和Ｎｄ同位素变异特征为依据，确定鲁苏榴辉岩为多成因、多来源和多阶段，指出主要是在印支期扬子陆块与华北陆块碰撞造山作用过程中，挤入的上地幔碎片以及不同原岩类型的壳内高压变质岩碎块。燕山晚期的区域构造热事件使得某些榴辉岩的同位素体系再平衡。     

Geochemistry and environment evolution of Core E in the Laizhou Bay since last stage of Middle Pleistocene

IwrincrIONOn the evolution of palcoenvironment, salt-water encroachmnt and the distributionof subsurface brine in the LaizhOu Bay area, many researches had been carried out, and muchknowledge abeut the gcolOgical features in this area since Late QUaternary was aCquired' ) (H8nand Wu, l992; Han and Meng, l994; Wen et al. l989). However there was IittIe studyon the sediment geOChemical characteristics since Quaternary. In this Paper, the element strati-graphic characteristics and evolut…     

Geochemical and hydrodynamic constraints on the distribution of trace metal concentrations in the lagoon of Nouméa, New Caledonia

Seawater samples were collected in the lagoon of Nouméa (southwest New Caledonia) along two transects from eutrophic coastal bays to the oligotrophic barrier reef. Land-based emissions to the lagoon were measured with dissolved and particulate concentrations of chromium (Cr) and nickel (Ni), used as tracers of both terrigenous and industrial (Ni ore treatment) activities, as well as dissolved and particulate concentrations of zinc (Zn), used as a tracer of urban effluents. The spatial variability of metal concentrations was related to geochemical and hydrodynamic conditions, i.e., respectively: (1) natural and anthropogenic emission sources, and chemical processes occurring in the water column; and (2) water residence times. The parameter used to describe the residence time of water masses was the local e-flushing time, i.e. the time required for a tracer mass contained within a given station to be reduced by a factor 1/e. High metal concentrations were found in coastal areas (up to 9000 ng dissolved Ni L⁻¹), and steeply decreased with distance from the coast (down to 101 ng dissolved Ni L⁻¹ near the barrier reef) to reach levels similar to those found in remote Pacific waters, suggesting a rapid renewal of waters close to the barrier. Distributions of metals in the lagoon are controlled upstream by land-based emission sources and later chemical processes. Then hydrodynamics constrain metal distributions, as shown by the observed relationship between local e-flushing times and the spatial variability of metal concentrations. In addition, a change in the direction of prevailing winds yielded a decrease of dissolved metal concentrations at the same site by a factor of 2.5 (Cr and Ni) and 2.9 (Zn). It is suggested that the residence time is a key parameter in the control of elemental concentrations in the lagoon waters, as much as land-based emission sources.