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.     

细菌、病毒与浮游植物相互关系及其对海洋地球化学循环的作用

本文综述了近年来国内外在海洋地球化学循环，特别是微生物环研究方面的发展现状，探讨了浮游植物，细菌，病毒相互之间的关系及其对海洋地球化学循环的影响。     

随机激励下非线性海洋结构物响应分析方法研究进展

对在随机载荷作用下非线性海洋结构物的运动响应分析的各种方法进行了综述,对有些方法的基本原理做了阐述,并指出一些最新的研究进展和今后进一步研究的方向。     

西菲律宾海沉积物铁族元素地球化学

本文对取自西菲律宾海区的三个柱状沉积物岩芯的铁族元素地球化学行为进行了系统的研究。从元素的含量及剖面变化、元素的相关性及组合特征,铁族元素与主元素的关系以及元素的赋存状态等方面探讨了物质来源、沉积作用和古气候,并据此进行了地层划分。沉积物有4种来源:海底火山源、生物源、自生源和陆源。海底火山物质提供了较多的铁族元素,相形之下,自生沉积作用较弱。元素地层学研究表明,在全新世温暖期和晚更新世寒冷期铁族元素表现出不同的地球化学行为,尤以Mn和亲生物(Ca)元素对气候的反映灵敏。WP_2孔和WP_(40)孔铁族元素特征相似,与WP_1孔差别较大。     

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.     

Optimum Sample Size to Detect Perturbation Effects: The Importance of Statistical Power Analysis – A Critique

Abstract. The current article describes statistical power analysis as an efficient strategy for the estimation of the optimum sample size. The principle aim is constructively to criticise and enrich the results presented by Mouillot et al. (1999) , who estimate the optimum sample size for evaluating possible perturbations. The authors did not make any reference to statistical power analysis, even though their objective clearly went beyond a simple stock evaluation to assess management strategies in a particular marine ecosystem. Surprisingly, they proposed (a priori) an ANOVA design to test a hypothesis considering both space and temporal scales. However, the authors did not cover important topics related with power analysis and the precautionary principle, both used into environment impact assessment programmes for marine ecosystems. Based on their results and on statistical power analysis, it is demonstrated that the variability (dispersion statistics), a key factor they used to estimate the sample size, is less relevant than the magnitude of perturbation (effect size). Therefore, a greater effort must be devoted to estimate the effect size of a particular phenomenon rather than a desired variability.     

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.     

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