冲绳海槽有孔虫壳体的微量元素Sr,Nd同位素地球化学

钙质生物壳的微量元素组合和Sr,Nd同位素组成是识别海底混合源沉积物中生物源物质相对贡献的重要参数.冲绳海槽有孔虫壳体强烈富集Sr,P,Mn和Ba,富集Li,U,Th,Sc,Co,Pb,Zn,Cr,Rb,Y,Sb和轻稀土元素,弱富集V,Ga,Zr,Nb,Cd和中稀土元素,相对贫Ge,Mo,In,Sn,Cs,Hf,Ta,W,Tl,Bi和重稀土元素,海水中微量元素的背景含量和生物活动对微量元素的选择性吸收是有孔虫壳体中微量元素发生富集和贫化的主要机制,冲绳海槽有孔虫壳体的稀土元素配分模式与海水和太平洋有孔虫的有明显差异,表现出中稀土元素相对富集,并具有微弱的负Ce异常.有孔虫壳体的Sr,Nd同位素比值也与大洋海水不同,分别为0.709769和0.512162,前者略高于大洋海水,后者略低于大洋海水,表明冲绳海槽海水明显受大陆河水影响.     

钙质成岩作用对有孔虫氧同位素的影响

通过对南海北部ODPl84航次1148站井深477m之下深海相渐新世浮游有孔虫Globoquadrina压扁壳、次生方解石和充填壳的氧同位素对比，定量分析了钙质成岩作用对壳体氧同位素的影响，结果发现，受成岩作用影响，1148站浮游有孔虫氧同位素显著变轻，这种变化趋势与低纬度开放性大洋明显不同。其原因可能与南海海盆扩张早期，大量陆源物质从较窄陆架可以直接沉积到海底，由于陆源物质氧同位素相对偏负，当与海洋沉积物混合后，引起本区沉积物孔隙水氧离子浓度变轻。而扩张初始，高的沉积速率可能使钙质壳体被快速封存在一个相对孤立的系统中，造成孔隙水离子成为影响壳体氧同位素变化的主要因素。当氧同位素相对较重的有孔虫壳体溶解和重结晶并与孔隙水离子发生交换时，引起壳体δ^18O负向偏移。     

南极冰退与深圳湾北岸海平面变化的地质记录

南极冰层的冰量为２４．５×１０６ｋｍ３，占地球总冰量的９０％以上，南极冰川进退控制着全球海平面变化和气候波动。酉部南极乔治王岛第四纪冰碛与湖积剖面记录了近１２０００ａ来南极曾于距今１１０００ａ，９０００ａ和６１００ａ出现过３次快速的冰消过程，近６０００ａ来是一小幅度冷暖交替的气候波动过程。深圳湾北岸潮间带堆积是在近６０００ａ以来发育的，堆积物的环境记录表明，海平面呈周期性升降变化，波动周期平均为６７０ａ，低海面时期发生于距今５５００—４９００ａ，３９００—３６００ａ，２４００—２２００ａ和１３００—１２００ａ。相邻低海面间则是海面上升时期，每一升降周期的海平面变化幅度为８０ｃｍ左右，近１００ａ的现代增温，海平面处于上升阶段，上升速率为２—３ｍｍ·ａ（－１）。     

大亚湾沉积物中重金属元素背景值研究

根据大亚湾的自然条件认为,大亚湾沉积物的物质来源是其周围集水区的岩石风化壳,并计算了其风化壳中重金属元素的平均丰度值;又根据沉积物的粒度和深层沉积物重金属元素的含量资料,列方程计算出湾内沉积物中重金属元素的平均含量,根据这两组数据,确定该区域内重金属元素的平均背景值。再通过粒度关系,计算得出大亚湾内各站沉积物中重金属元素的背景值。应用此结果和大亚湾沉积物重金属元素实测结果,计算了由人为影响带入沉积物中的重金属元素含量,了解其受污染的程度。     

中太平洋铁锰结壳铅同位素研究

已有研究表明大洋中溶解的铅(Pb)来源于陆源物质，但是，对Pb进入大洋的途径争议很大。为此分析了取自中太平洋两块铁锰结壳样品的Pb同位素组成，获得了整个新生代的中太平洋Pb同位素演化历史。结果表明这两块结壳的Pb同位素随时间的演化曲线与中北太平洋沉积物岩心LL44-GPC3中风成碎屑的Pb同位素演化曲线相似。证实该区深水中的天然溶解铅主要来自风成粉尘，并且50Ma之前中太平洋中溶解Pb同位素组成主要取决于源自美洲的风成粉尘的输入，40Ma之后主要取决于源自亚洲的风成粉尘的输入。     

Trace element diagenesis in pyrite-rich sediments of the Achterwasser lagoon, SW Baltic Sea

The early diagenesis of trace elements (V, Cr, Co, Cu, Zn, As, Cd, Ba, U) in anoxic sediments of the Achterwasser, a shallow lagoon in the non-tidal Oder estuary in the Baltic Sea, was investigated in the context of pyrite formation. The dissolved major redox parameters show a two-tier distribution with transient signals in the occasionally re-suspended fluid mud layer (FM) and a permanently established diagenetic sequence in the sediment below. Intense microbial respiration leads to rapid depletion of O₂ within the uppermost mm of the FM. The reduction zones of Mn, Fe and sulfate overlap in the FM and in the permanently anoxic sediment section which appears to be a typical feature of estuarine sediments, under low-sulfate conditions. Degrees of pyritization (DOP) range from 50% in the FM to remarkably high values > 90% at 50 cm depth. Pyrite formation at the sediment surface is attributed to the reaction of Fe-monosulfides with intermediate sulfur species via the polysulfide pathway. By contrast, intense pyritization in the permanently anoxic sediment below is attributed to mineral growth via adsorption of aqueous Fe-sulfide complexes onto pyrite crystals which had originally formed in the surface layer.The studied trace elements show differential behavior patterns which are closely coupled to the diagenetic processes described above: (i) Zn, Cu and Cd are liberated from organic matter in the thin oxic layer of the sediment and diffuse both upwards across the sediment/water boundary and downwards to be trapped as monosulfides, (ii) V, Cr, Co and As are released during reductive dissolution of Mn- and Fe-oxyhydroxides, (iii) U removal from pore water occurs concomitantly to Fe reduction in the FM and is attributed to reduction of U(VI) to U(IV), (iv) the Ba distribution is controlled by reductive dissolution of authigenic barite in the sulfate reduction zone coupled with upward diffusion and re-precipitation. The incorporation of trace elements into pyrite is most intense for Co, Mn and As, intermediate for Cu and Cr and little to negligible for U, Zn, Cd, V and Ba. The observed trend is largely in agreement with previous studies and may be explained with differing rates for ligand exchange. Slow and fast ligand exchange and thus precipitation kinetics are also displayed by downcore increasing (Mn, Cr, Co and As) or constantly low (Zn, Cu, Cd) pore water concentrations. The downward increasing degrees of trace metal pyritization (DTMP) for Co, Cu, Zn and As are, in analogy to pyrite growth, assigned to adsorption of sulfide complexes or As oxyanions onto preexisting pyrite minerals.     

Trichodesmium erythraeum (Ehrenberg) bloom along the southwest coast of India (Arabian Sea) and its impact on trace metal concentrations in seawater

The incidence of a large scale Trichodesmium erythraeum bloom along the southwest coast of India (Arabian Sea) observed in May 2005 is reported. Around 4802 filaments of T. erythraeum ml⁻¹ seawater was observed and a colony consisted of 3.6 × 10⁵ cells. The bloom was predominant off Suratkal (12° 59′N and 74° 31′E) with a depth of about 47 m, covering an area of 7 km in length and 2 km width. The concentrations of Zinc, Cadmium, Lead, Copper, Nickel and Cobalt were determined in samples collected from the bloom and non-bloom sites using stripping voltammetry. The observed hydrographical and meteorological parameters were found to be favorable for the bloom. The concentrations of Zinc, Cadmium and Nickel were found to be higher at bloom stations, while the concentrations of Lead, Copper and Cobalt were found to be very low at bloom stations. Elevated concentrations of Cadmium and Cobalt were observed at Valappad mainly due to the decomposition of detrital material produced in the bloom. Statistically significant differences (P > 0.01) in metal concentrations between the bloom and non-bloom stations were not observed except for Copper. Metals such as Lead, Copper and Cobalt were removed from the seawater at all places where bloom was observed. Cadmium was found to be slowly released during the decaying process of the bloom.     

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。     

安徽宣城地区中晚更新世风成堆积与环境变迁

通过对宣城向阳中晚更新世沉积剖面的综合研究,认为该剖面与中国北方同时代的黄土—古土壤剖面相比较,虽然长江下游以南地区中晚更新世多个冰期中风成堆积的单层厚度与累积厚度,亦即风成物质的沉积通量与沉积速率均比北方黄土区要小,但它们所反映的气候与环境的变化具有明显的可比性。