Retention of arsenic and phosphorus in iron-rich concretions of Tagus salt marshes

Iron-rich concretions are frequently found around plant roots in Tagus estuary (Portugal) where radial delivery of O₂ takes place. Salt marsh sediments exhibit cracks that are an additional feature to introduce O₂ and other solutes in the upper sediments. Metal concentrations in salt marsh sediments are clearly above the background levels reflecting the anthropogenic sources from a large city with 2.5 million inhabitants, and several industrial centres. In order to evaluate how both oxidised structures influences the redistribution of redox sensitive elements in salt marsh sediments, concretions were collected from roots of Halimione portucaloides below the oxygenated zone. These tubular cylindrical structures were analysed for Fe, Al, Mn, As, and P along 1-cm radial transect in a millimetre scale from the inner part to the adjacent anoxic sediment. In addition, oxidised cracks were analysed for the same spatial resolution, from the sediment–water interface to anoxic layers (2-cm transept). The parallelism between Fe, As, and P concentrations at this microscale is the most noticeable aspect. Iron and As presented very high concentrations in the 4-mm concretions (3.4 mmol g⁻¹ and 3.1 μmol g⁻¹, respectively) and decreased sharply to the host sediment. Oxygen released from roots oxidise the solid sulphides, and the reduced Fe and As are transported towards the root by both diffusion and pore water flow associated with the root water uptake. Subsequently, Fe(III) precipitates and As is retained by sorption and/or coprecipitation. These elements are also enriched in the first 2-mm of oxidised cracks, but in lower concentrations (50% and 30%, respectively). Manganese concentrations in concretions were low (11.8 μmol g⁻¹), indicating that Fe dominates the sediment chemistry. Phosphorus and iron concentrations in the ascorbate fraction were higher in the oxidising surfaces of concretions (10.7 μmol g⁻¹ and 1.6 mmol g⁻¹, respectively) and of cracks (5.1 μmol g⁻¹ and 0.47 mmol g⁻¹). The parallelism of Fe and As distributions includes not only their similar redox chemistries, but also that to phosphate, including control by coprecipitation of the host iron phases. The mechanisms involved in the mobilisation of As and P are however different, whereas As comes from the oxidation of iron sulphides; dissolved P derives from reduction of ferri-hydroxide phases.     

Advances in the Study of Geochemistry and Paleo-oceanography of the Co-rich Crust

The current advances in the study of geochemistry and paleo-oceanography of the Co-rich crust are reviewed in this paper. We summarize the study of geochemistry of the Co-rich crust, discuss the diffusion of elements in the Co-rich crust and the exchange with ambient seawater. Besides, we discuss the effect of phosphatization and substrate rocks on the composition of the Co-rich crust. We also introduce the application of stable isotopes (including the stable isotopes of Pb, Nd, and Hf), radioactive isotopes (including the radioactive isotopes of Be, U and Th), and elements (including the major elements, minor elements and rare earth elements) to the study of paleo-oceanography of the Co-rich crust.     

青岛—石臼所沿岸潮流特征分析

本文对青岛—石臼所沿岸潮流特征进行了分析。实际观测资料表明,这一带潮流具有典型的往复流性质,并有较明显的不对称性和较大的垂直变化。文中指出涨落潮流不对称性是由于余流和分潮流影响的结果。讨论了不对称性随余流和分潮流的变化和潮流垂直梯度的特征。不对称和垂直梯度对泥沙运动和污染扩散的影响在文中也作了阐述。     

东太平洋沉积物U的地球化学

本文对地矿部“海洋四号”科学考察船１９８７－１９８９年在东赤道太平洋ＣＣ区所取得的２７个深海表层沉积样品进行Ｕ的地球化学分析，探讨了Ｕ在深海沉积中的地球化学行为，结果表明，不同类型沉积的Ｕ含量不同，平均值由大至小的次序的含沸石粘土（２．１６×１０＾－６），硅质粘土（１．９５×１０＾－６），硅质软泥（１．６５×１０＾－６），钙质硅质粘土（１．５９×１０＾－６），在同类型沉积中Ｕ的分散性较大；Ｕ在区域     

南海西沙西南海域表层沉积物特征

西沙西南海域表层沉积物样品矿物成分，地球化学，微体古生物分析测试结果表明：沉积物可分为７种类型，沉积环境主要是陆坡，部分为深海平原，海洋生物，海洋化学以及火山物质的沉积起到了积极的作用，陆源物质的影响较小，它们主要来源于北部大陆和南部岛礁等物源区。     

氧同位素分析在东濮凹陷下第三纪沉积环境中的应用

主要介绍了氧同位素的地球化学特征，并利用这些特征在沉积环境方面的指示意义，分析了东濮凹陷下第三系盐湖沉积的氧同位素。分析结果表明：尽管保存在碳酸盐中的氧同位素的值不能定量地反映原始氧同位素的值，不能够作为区分海陆相的标志，但它可以定性地探讨碳酸盐沉积时的沉积环境。通过对东濮凹陷下第三系盐湖沉积的氧同位素分析发现，从沙四上到沙一时期，除了沙三上的δ^18O有些突变外，基本上呈递增趋势。这反映出，从沙四上到沙一时期该区的气候逐渐向干早过渡；沙四上到沙三上一段δ＾18Ｏ明显比沙一和沙二上伯低，说明在沙四上到沙三上时期，该沉积区的蒸发作用还不是很显著，而另一方面也说明在由沙三上向沙二上过渡时，该区可能存在一次气候突变，使得沙二上和沙一时期的蒸发量远大于降雨量，δ^18O的值也因此迅速增大。同时，也做了碳酸盐同位素系数Z值的研究，其揭示的沉积环境特征与氧同位素基本相同。     

台湾海峡中、北部及邻近海域夏季浮游动物总生物量的分布特点

台湾海峡中、北部夏季浮游动物（非胶质）总生物量较丰富，1983年夏季的总生物量高于其他季节，1987年7、8月和1988年7月则高于1983年同期的生物量，这3a的高生物量分布区，一般都连片出现在上升流锋面区，显然和上升流的出现有密切关系。构成高生物量的优势种以外海广高盐种为主，生物量和高生物量区的分布态势都存在年际变化，这可能和不同性质水系的消长，相互推移及被囊动物的摄食竞争有关。     

东亚温带气旋及其长期预报（一）—气候特征及其影响因素

本文分析了影响我国近海的温带气旋气候特征及其影响因素。分析得出：３－７月是温带气旋的盛季，４月份是全年中温带气旋最多的月份。赤道东太平洋海温异常增暖的年份，温带气旋增多。     

大西洋中脊热液硫化物的矿物学研究

利用１９８９年在大西洋热液活动区采集的块状硫化物样品，采用矿相显微镜、电子显微镜和电子探针等手段，进行了矿物共生组合、矿物形态与成分标型及其演化特征研究。结果表明，大西洋热液成矿作用可以划分为热液期与沉积期两个成矿期，和石英－黄铁矿阶段、黄铁矿阶段、多金属硫化物阶段、胶状黄铁矿阶段和非晶质ＳｉＯ２阶段等５个成矿阶段；不同成矿阶段黄铁矿的共生矿物和矿物特征不同，在晶体形态上具有从单形晶－聚形晶－胶状     

长江口南支沉积物元素地球化学分区与环境指示意义

对采自长江口南支的130个表层底质沉积物样品采用X射线荧光光谱法进行了20种常、微量元素的地球化学分析。在此基础上,应用系统聚类法对该区域进行了元素地球化学分区。研究结果表明,研究区主要可以分为两大地球化学分区:Ⅰ区以相对富集SiO2,Sr,Zr元素为典型特征,主要涵盖5 m等深线以浅的长江三角洲前缘区;Ⅱ区以相对富集Al2O3,TFe2O3(全铁),MgO,Pb元素为典型特征,涵盖了前三角洲的广大区域。从地球化学分区的空间分布来分析,这两个分区元素之间的差异反映的是沉积水动力条件与沉积介质物化性质这两个环境要素空间分布的差异性,即在研究区内,表层沉积物元素地球化学空间分布的差异性实质上反映了沉积环境空间分布的差异性。