东太平洋粘土沉积物组成和结构分析

对东太平洋-中国大洋调查区粘土沉积物组成和结构进行了分析,并根据其物相组成划分了7个沉积物类型,其中以伊/蒙 高岭石 石英型沉积物中粘土矿物含量最高;IR分析证明东太平洋粘土沉积物中富含有机质;对沉积物粒度分布和XRD测试结果显示,东太平洋粘土与地表同类粘土相比粒度明显细小且结晶差;SEM结果显示东太平洋粘土矿物为絮状和片状;综合分析东太平洋粘土的结构特征认为其活性比地表同类粘土大,预示该地区海洋粘土将会有更好更广的用途.     

中太平洋海盆表层沉积物及其与锰结核的关系

通过对中太平洋海盆表层沉积物与相伴生的锰结核的研究表面,丰度、品位等有明显的差异,在深海粘土中锰结核干度最度,钙质软泥多,锰结核的发现聚集与沉积物类型,沉积速率、孔隙度、金属含量及形成时的氧化还原条件,水深、底层流等的影响.锰结核的形成,发育与富集是受多种因素所控制,是一个模式内的约制。     

太平洋西部深海沉积物中Fe、Mn、Mg地球化学

本文详细描述了取自太平洋西部7个岩心沉积物中Fe、Mn，Me的分布、来源及地球化学特征。由于Fe、Mn、Mg的含量与火山碎屑矿物和沉积物类型有关，这对太平洋西部的沉积环境起着标志作用。     

太平洋CC区西部沉积物地球化学特征及其成因

对太平洋CC区西部7根沉积物短柱样的常微量元素进行浓度测试,以了解沉积物元素时空分布特征及其来源和控制因素.与上地壳元素平均值(UCC)相比,研究区沉积物中MnO、P2O5、Co、Ni、Cu、Mo、Ba明显富集,Al2O3、K2O、Fe2O3、CaO、Sr等亏损.聚类和因子分析表明研究区沉积物元素有4种来源,其中Al2...     

东太平洋洋底沉积物的物质组成与物理化学特征

作者通过研究,发现东太平洋洋底沉积物主要是由<0.063mm的伊利石、蒙脱石加混层矿物、高岭石、绿泥石粘土矿物和放射虫、硅藻等组成。具有碱性、比表面积大,离子交换容量大的特点。该成果无异为东太平洋多金属结核分布区的大洋地质学的研究,提供了可贵的环境地质资料。     

太平洋中部富REY深海沉积物的地球化学特征及化学分类

赋存于深海沉积物中的稀土资源是一种潜在的稀土资源。对太平洋中部30个重力活塞柱状样中的1 275个深海沉积物样品的常量、稀土化学分析数据进行了系统研究。在涂片鉴定的基础上,采用Ca O和Al2O3含量把太平洋中部深海沉积物划分为钙质软泥类沉积物、硅质软泥类沉积物、深海黏土类沉积物三种成因类型;这三种类型沉积物的稀土分布模式相似,表现为明显的Ce负异常,一定程度的重稀土元素富集和Y正异常,深海黏土类沉积物的ΣREY明显偏高。采用主要元素(包括Ca O/P2O5比值)与REY的关系图可以有效地判别不同成因类型沉积物的混合状况。太平洋中部富P、富含沸石的深海黏土类沉积物是最有利的富REY的深海沉积物类型。太平洋中部深海沉积物REY富集的主要原因是由于深海沉积物中混入了过量的(鱼牙骨碎屑状)磷灰石组分,而钙质生物组分和硅质生物组分的加入对REY含量起了明显的稀释作用。     

东太平洋深海沉积物小于2μm组分的稀土元素地球化学特征

用等离子光谱测定了东太平洋９个深海沉积物样品的小于２μｍ组分及全岩的稀土元素,结果显示,小于２μｍ组分及全岩的稀土元素组成均受控于沉积物类型,而二者之间稀土元素组成的差异在钙质和硅质沉积物中出现相反的趋势。元素相分析和稀土元素赋存状态分析表明,这种差异主要由于沉积物物质组成的不同所致,表面在化学组成上,主要与ＭｎＯ,Ａｌ２Ｏ３Ｆｅ２Ｏ３,ＣａＯ含量的变化有关,大多数样品在小于２μｍ组分的稀土组成     

太平洋北部铁锰结核富集区沉积物的元素地球化学特征

本文对太平洋北部铁锰结核富集区沉积物的元素地球化学作了较为详细的研究。因子分析提供的信息表明,元素的分布主要受三个因子控制:（1）粘土及Fe、Mn氧化物水化物胶体的吸附作用;（2）生物化学作用过程有关的自生沉积作用;（3）海底页岩风化及附近海区的火山喷发作用。元素的来源:（1）Fe、Mn、Cu、Co、Ni、Zn、Cr、Cr、Mg、Al、Ti、K共生,主要来自粘土吸附;（2）C_有机、N、Sr、Na及Si、Ca、Sr主要来自生物化学过程沉积;（3）Pb主要来源于岩石碎屑（火山喷发碎屑）。     

中太平洋CC区表层沉积物的地球化学

根据对中太平洋CC区表层沉积物常量、微量元素的测试结果,采用多元统计分析的方法,研究了该地区表层沉积物中元素含量的空间分布和组合特征,探讨了其物质来源及沉积环境的横向演变规律.元素的相关性分析和R型因子分析表明,SiO2、Al2O3、Fe2O3、MgO、K2O、Na2O等常量元素氧化物之间存在明显的正相关关系,说明这些元素氧化物内在关系较为密切,在沉积物中所起的作用相近,元素的地球化学行为相似,尤其在成因方面专属性较强,主要受陆源碎屑沉积及火山活动的影响.它们与CaO、CaCO3、Sr为明显的负相关关系,说明二者内在关系比较疏远,相关性差,沉积物源不同,后者主要与生物作用有关.由SiO2、Fe2O3、TiO2与Al2O3的比值与Ba/Sr标准值对比显见,中太平洋CC区表层沉积物主要来源于深海黏土、生物源和火山热液活动的产物.沉积相主要为硅质软泥相、硅质黏土相、钙质软泥相、沸石黏土相.     

Remobilization of transition metals in surficial pelagic sediments from the eastern Pacific

The top thirty centimeters of sediment at two sites in the eastern equatorial Pacific contain evidence of post-depositional remobilization of Mn, Fe, Co, Ni, Cu, and Zn. Remobilization takes place as Mn and Fe oxyhydroxides are released to the pore water during the microbially-mediated decomposition of organic matter. Precipitation of the dissolved metals in near-surface more oxic strata controls the solid-phase distribution of Mn, Fe, and Zn. The solid-phase redistribution of Co and Ni requires only suitable material for readsorption. Comparison of pore water fluxes with solid-phase metal distributions in the solid sediment indicates no loss of dissolved metal to the overlying water column at the present time. Loss of Mn during the Quaternary is indicated by the composition of the sediments, however. Leaching experiments suggest that portions of the mobile Mn, Fe, Co, Ni, and Cu are fixed by incorporation in authigenic smectite in the surficial sediments.     

Chemical fractionation of transition elements in Pacific pelagic sediments

Partitioning of transition elements in Pacific pelagic sediments (35 samples) was performed by sequential chemical leaching with barium chloride/triethanolamine (easily extractable fraction), acidic cation exchange resin (carbonate phases), and hydroxylamine hydrochloride and dilute hydrochloric acid solutions (hydrous oxides). Residual metal percentages are highest in red-brown clays and siliceous ooze, intermediate in calcareous materials and low in micronodules (2 samples, > 125 μm): residual metal contents seem to be controlled predominantly by the rate of admixture of volcanoclastic materials. At higher bulk metal concentrations, the non-residual fractions of Mn, Cu, Ni and Zn generally increase both in red-brown pelagic clays and in siliceous ooze. Mn, Ni, and Co concentrations are mainly associated with the easily reducible fraction (0.1 M NH₂OH·HCl), whereas Fe, Cu, and Zn exhibit higher percentages in the hydrochloric acid soluble fractions (0.3 M HCl); Zn and Cu are associated to some extent with the carbonate phase, copper with the easily extractable fraction.     

Oxygen consumption rates in pelagic sediments from the Central Pacific: First estimates from microelectrode profiles

Oxygen profiles in pelagic sediments from the Manganese Nodule Program calcareous and siliceous ooze sites (MANOP sites C and S) in the central Pacific Ocean were measured with microelectrodes and are used to predict oxygen consumption rates beneath the sediment-water interface. We explain possible artifacts which occur during sample recovery and argue that minimum estimates of 0.083 and 0.025 μ moles $\text{O}{}_2\text{cm}{}^2\text{day}$ (C and S, respectively) can be calculated from the data. These oxygen consumption rates are in good agreement with in situ respirometer measurements previously reported for comparable sediments in the north Pacific, but previous estimates based on modeling of pore water nitrate profiles at both sites are two to five times smaller than our minimum fluxes. The differences in oxygen fluxes calculated by the two methods are probably in part due to uncertainty in the assumptions inherent in the nitrate model. However, non-steady state fluctuations in particulate organic matter fluxes could also be a reason for the disparity.     

中国多金属结核开辟区沉积物中微量元素地球化学特征

分析了中国多金属结核开辟区沉积物中Ba、Ce、Co、Cr、Cu、Mo、Ni、Sr、V、Y和Zn等11个微量元素的含量。研究表明，开辟区沉积物中微量元素在不同沉积单元中的分布特征存在明显差异，反映了地质历史上沉积环境的不同。沉积物中的Zn、Ni和Mn具有共同来源，反映铁锰氧化物、氢氧化物对这些元素的吸附控制作用；Sr、Ba以及Ce和Y等元素在东区主要与岩源碎屑有关，而西区则主要来自生物碎屑；Cu具有多种来源，东区主要与生物组分和岩源碎屑有关，西区则主要与自生铁锰氧化物的吸附有关。而通常认为与有机物有关的Cr、V等元素在研究区内则主要来自岩源碎屑。     

Interelement relationship in abyssal Pacific ferromanganese nodules and associated pelagic sediments

By R-mode factor analysis and enrichment factor calculations, most of the elements in abyssal ferromanganese nodules and associated pelagic sediments (excluding common authigenic minerals like apatite, barite, opal and carbonates) are found to be preferentially concentrated in one of the following three major phases: aluminosilicates (e.g., Al, Si, Sc, Ga, Cr, Be, Na, K, Rb and Cs), Fe-oxides (e.g., Fe, P, S, V, Se, Te, As, B, Sn, U, Hg, Pb, Ti, Ge, Y, Zr, Nb, Pd, In, rare-earths, Hf, Th, Pa, Pu, Am, Ru and Bi), and Mn-oxides (e.g., Mn, Tl, Ag, Cd, Mg, Ca, Ba, Ra, Co, Ni, Cu, Zn, Mo, Sb and probably W). The specific association of elements with these three phases can be explained by the difference in chemical forms of elements in seawater and by fundamental differences in physicochemical properties (e.g., the pH of zero point of charge and dieletric constant) of these three phases.     

Early oxidation of organic matter in pelagic sediments of the eastern equatorial Atlantic: suboxic diagenesis

Pore water profiles of total-CO₂, pH, PO^3?₄, NO^?₃ plus NO^?₂, SO^2?₄, S^2?, Fe²⁺ and Mn²⁺ have been obtained in cores from pelagic sediments of the eastern equatorial Atlantic under waters of moderate to high productivity. These profiles reveal that oxidants are consumed in order of decreasing energy production per mole of organic carbon oxidized (O₂ > manganese oxides ~ nitrate > iron oxides > sulfate). Total CO₂ concentrations reflect organic regeneration and calcite dissolution. Phosphate profiles are consistent with organic regeneration and with the effects of release and uptake during inorganic reactions. Nitrate profiles reflect organic regeneration and nitrate reduction, while dissolved iron and manganese profiles suggest reduction of the solid oxide phases, upward fluxes of dissolved metals and subsequent entrapment in the sediment column. Sulfate values are constant and sulfide is absent, reflecting the absence of strongly anoxic conditions.     

Geochemistry of the rare earth elements in ferromanganese nodules from DOMES Site A,northern equatorial Pacific

The distribution of rare earth elements (REE) in ferromanganese nodules from DOMES Site A has been determined by instrumental neutron activation methods. The concentrations of the REE vary markedly. Low concentrations characterize samples from a depression (the valley), in which Quaternary sediments are thin or absent; high concentrations are found in samples from the surrounding abyssal hills (the highlands) where the Quaternary sediment section is relatively thick. Moreover, the valley nodules are strongly depleted in the light trivalent REE (LREE) and Ce compared with nodules from the highlands, some of the former showing negative Ce anomalies.The REE abundances in the nodules are strongly influenced by the REE abundances in coexisting bottom water. Some controls on the REE chemistry of bottom waters include: a) the more effective removal of the LREE relative to the HREE from seawater because of the greater degree of complexation of the latter elements with seawater ligands, b) the very efficient oxidative scavenging of Ce on particle surfaces in seawater, and c) the strong depletion of both Ce and the LREE in, or a larger benthic flux of the HREE into, the Antarctic Bottom Water (AABW) which flows through the valley. The distinctive REE chemistry of valley nodules is a function of their growth from geochemically evolved AABW. In contrast, the REE chemistry of highland nodules indicates growth from a local, less evolved seawater source.     

Geochemical control of magnetite dissolution in subarctic lake sediments and the implications for environmental magnetism

Geochemical and mineral magnetic studies of lake sediments from the Kårsa valley in north Sweden demonstrate that down-core variations in magnetic properties have been determined by post-depositional magnetite dissolution rather than by sediment source changes. A low sediment accumulation rate during times of climatic amelioration combined with a higher organic carbon content produced intense reducing conditions with almost complete magnetite loss. An increase in the sedimentation rate and a reduction in the organic carbon content, primarily due to glacier reformation, allowed magnetite preservation. Thus the mineral magnetic profiles record lake sediment palaeoredox conditions brought about by climate change. This new interpretation of mineral magnetic transformations in freshwater sediments may have far reaching implications for other mineral magnetic studies concerned with the alternation between glacial (stadial) and interglacial (interstadial) episodes during the Quaternary period.     

Geochemistry of barium in pelagic sediments

High concentrations and accumulation rates of Ba occur on active (spreading) ridges, and in some areas of high biological productivity. These patterns show that Ba is deposited on the deep sea floor by both volcanic and biological processes.