深海生源碳酸盐沉积物形成研究及其环境意义

生物源碳酸盐是海洋沉积物的组成部分,在深海更是如此,钙质软泥约占大洋面积的一半、全球面积的四分之一。深海造碳酸盐生物与浅海不同,主要不是底栖生物而主要是浮游生物,其中以浮游有孔虫、颗石藻、浮游软体动物翼足类、异足类等主物群最多。当生物碎     

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。     

北太平洋铁锰结核富集区沉积物和间隙水中重金属元素地球化学

对北太平洋28个相对富集铁锰结核的沉积物和间隙水中重金属元素(Cu、Pb、Zn、Cr、Co、Ni)地球化学研究表明:沉积物中重金属元素明显的比陆地土壤、河口、陆架及贫结核洋区的沉积物富集,并与沉积物类型密切有关;沉积物中元素的赋存状态不同,进入间隙水的途径不同;由于Cu、Co的生物作用大于Zn、Ni,使沉积物中 Cu/Zn、Co/Ni比值由钙质软泥—钙、硅软泥—硅质软泥—褐色粘土升高。     

太平洋调查区沉积物中某些金属元素的地球化学探讨

通过对大洋锰结核及其伴生沉积物研究,发现锰结核与粘土组分和有机物(或生物)有关,故笔者试图了解太平洋调查区沉积物中某些金属元素的地球化学行为。研究发现,随海水的加深,沉积物中 Ca、Sr 含量减少,其他元素含量升高,沉积物类型由钙质软泥→硅钙质软泥→红粘土。在4000—6000m 水深范围内,锰结核丰度随海水深度     

太平洋中部富REY的深海沉积物的地球化学特征及化学分类

<正>深海沉积物中的稀土资源是潜在的海底稀土资源。本文对太平洋中部重力柱取样获得的1275个深海沉积物样品的矿物组分、常量、稀土化学分析结果进行了系统分析,并与中北太平洋海域990个深海沉积物样品的稀土元素地球化学特征进行了对比。分析研究结果表明太平洋中部深海沉积物样品的富REY的地球化学特征与中北太平洋相似。首先太平洋中部深海沉积物样品根据Ca O含量可分为两类:⑴Ca O≥10%,代表了富含钙质生物组分的沉积物类型,与沉积物分类中的钙质软泥相当,其ΣREY     

西太暖池区生物组分对海底表层沉积物物理力学性质的影响

西太平洋暖池区是指位于热带西太平洋及印度洋东部海表温度常年在28 ℃以上的海域,是全球海表温度最高的深海区,构造环境与沉积环境复杂,沉积物中的生物组分含量差异较大,生物组分会对深海沉积物物理力学性质产生显著影响,但目前对沉积物中生物组分含量和沉积物物理力学性质之间的相关性关系尚不明确。本文对西太平洋暖池区核心部位的表层沉积物样品进行现场物理力学性质测试和室内涂片鉴定,研究深海表层沉积物的物理力学性质与生物组分之间的关系。结果表明:研究区表层沉积物含水率范围为61.1%~435.1%,天然密度范围为1.04~1.76 g/cm³,贯入阻力范围为0~100 kPa,十字板剪切强度范围为0~8.6 kPa,整体具有高含水率、低密度、低强度等典型的深海沉积物物理力学性质特点。西加洛林海脊、海山等CCD以浅的区域为钙质生物组分>50%的钙质沉积区;西加洛林海槽西南部及其周边的深水沟槽地区一般为硅质生物组分>50%的硅质沉积;西加洛林海盆内部则主要为黏土沉积区。随钙质生物组分减少和硅质生物组分增多,表层沉积物类型分别为钙质沉积物、黏土沉积物和硅质沉积物,天然含水率变高,天然密度、贯入阻力和十字板剪切强度降低,表明深海表层沉积物的物理力学性质与生物组分含量密切相关:贯入阻力、十字板剪切强度、天然密度与钙质生物组分含量呈正相关,与硅质生物组分含量呈负相关;而天然含水率正好相反,与钙质生物组分含量呈负相关,与硅质生物组分含量呈正相关。本文建立了深海沉积物中生物组分与物理力学性质之间的相关关系,提出了沉积物生物组分含量与物理力学性质之间的拟合公式,可以为深海沉积物工程性质的评价提供参考。     

深海粘土和软泥的形成、分布及其控制因素

粘土和软泥是组成世界各大洋深海沉积物的主要成分,作为非传统的矿产资源,它们的储量巨大,开采、运输技术却相对其他深海矿产资源简单.而且,由于赋存条件特殊,深海粘土和软泥在粒度、成分、结构、活性等方面具备很多优于地表同类资源的特性(张海平等2005),因而在建材、冶金、化工、生物、石油、纺织、食品、水利、交通、医药、保健等领域具有潜在应用价值.目前,世界上许多国家正在积极开展这方面的研究工作.本文简单总结了深海粘土和软泥资源的形成、分布及其控制因素.     

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。     

Comparative study on the geochemical characteristics of rare earth elements in deep-sea sediments from different regions of the Pacific OceanSCIEI北大核心CSCD

太平洋深海沉积物中富集稀土元素(REY,包括钇),被认为是富有潜力的新型稀土资源。(含)沸石粘土、深海粘土和多金属软泥是主要的富含REY的沉积物类型,其中(含)沸石粘土和深海粘土在中、西北太平洋海盆大面积分布,而多金属软泥则多分布于靠近东太平洋洋脊热液活动的深海盆地中。目前关于中、西北太平洋海盆的深海粘土和(含)沸石粘土已有较多的研究,但关于多金属软泥中REY的研究较少。不同区域、不同类型深海沉积物中的稀土元素赋存状态有何差异?影响稀土富集的机制又是什么目前尚不清楚,也就进一步影响了对深海沉积物稀土资源的勘查和开发工作。本文分析对比了太平洋不同区域不同类型深海沉积物的地球化学特征及矿物学特征。结果表明,总体上,中、西北太平洋海盆深海沉积物中,尤其是(含)沸石粘土中的REY含量明显高于东太平洋海盆多金属软泥REY含量,其REY的富集主要与磷酸盐有关。超常富集REY(∑REY>2000×10^(-6))的沉积物中的CaO/P_(2)O_(5)比值趋向于一致(~1.4),几乎接近于磷灰石CaO/P2O5比值(~1.3),因此REY主要赋存载体为磷灰石,该区沉积物中REY的富集可能受到磷酸盐化的影响;东太平洋海盆多金属软泥明显受到热液影响,铁和锰的含量明显增加,但其∑REY含量集中于500×10^(-6)~800×10^(-6),不随铁和锰的增加而变化,REY的富集仍与磷酸盐关系密切,而与铁锰物质和铝硅酸盐关系不大。中、西北太平洋海盆富稀土的深海沉积物形成时处于较强的氧化环境,同时又有充足的含磷物质补给,才造成REY在该区沉积物中的超常富集;而东太平洋海盆多金属软泥虽然处于氧化环境,但缺少足够的磷补给,所以其∑REY含量通常低于中、西北太平洋海盆沸石粘土中∑REY含量。     

印度洋洋盆BC02站位表层沉积物地球化学特征及其物源指示意义

沉积物类型和物质来源对于深海固体资源的勘探调查和成矿理论研究具有重要意义。近年来的相关研究表明,中印度洋洋盆南部可能分布富含稀土元素的深海黏土沉积区和含铁锰结核硅质沉积区,但是目前该区域相关研究较少。对大洋第34航次在中印度洋洋盆所获取的BC02站位箱式沉积物样品进行了主量元素、微量元素以及稀土元素含量分析测试,结果表明,研究区沉积物主要为硅质生物沉积,可能有陆源物质和火山物质的输入,但是贡献均较少,没有发现铁锰结核存在,该区域受较强烈的硅质生物沉积稀释作用,区域内稀土元素的质量分数平均值为265.41×10-6,富集程度和富集特征与正常的硅质软泥基本一致,而与中印度洋洋盆和Wharton海盆已经发现的富稀土深海黏土明显不同,沉积环境为稳定的偏氧化环境。     

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。     

川南下志留统龙马溪组页岩岩相表征

页岩岩相表征是页岩气地质评价和选层、选区的基础性研究工作。本文以露头和钻井资料为基础,依据岩矿、薄片、地化和测井资料,建立了海相页岩岩相划分方法,对川南上奥陶统五峰组下志留统龙马溪组主要岩相进行了精细表征,并形成4点认识：(1)应用岩石矿物三端员法+沉积微相划分页岩岩相类型及其组合,是开展海相页岩岩相表征的有效方法;(2)川南五峰组龙马溪组页岩发育6种岩相类型和3种典型岩相组合,其中硅质页岩和钙质硅质混合页岩是(半)深水环境的特有岩相,黏土质页岩和黏土质钙质混合页岩是半深水浅水环境的主要岩相,黏土质硅质混合页岩是浅水深水环境下的共有岩相;(3)随着水体由深变浅和水动力条件逐渐增强以及陆源物质输入量增大,不同成因岩相组合的页岩矿物成分、基质组构、古生物和有机质富集程度、测井响应等基本特征均发生重大变化;(4)受海平面变化控制,主力产层为深水陆棚沉积的硅质页岩、钙质硅质混合页岩和黏土质硅质混合页岩组合,产层顶板为半深水浅水陆棚沉积的黏土质页岩、黏土质硅质混合页岩和黏土质钙质混合页岩组合;前者因富含硅质和有机质,具有良好的脆性和物性,是形成页岩气产层的优质岩相;后者因富含黏土和贫有机质,脆性和渗透性差,是形成页岩气藏区域封盖层的优质岩相;两者自下而上构成良好的自封自储型储盖组合。     

Geochemistry of ferromanganese nodule–sediment pairs from Central Indian Ocean Basin

Fourteen ferromanganese nodule–sediment pairs from different sedimentary environments such as siliceous ooze (11), calcareous ooze (two) and red clay (one) from Central Indian Ocean Basin (CIOB) were analysed for major, trace and rare earth elements (REE) to understand the possible elemental relationship between them. Nodules from siliceous and calcareous ooze are diagenetic to early diagenetic whereas, nodule from red clay is of hydrogenetic origin. Si, Al and Ba are enriched in the sediments compared to associated nodules; K and Na are almost in the similar range in nodule–sediment pairs and Mn, Fe, Ti, Mg, P, Ni, Cu, Mo, Zn, Co, Pb, Sr, V, Y, Li and REEs are all enriched in nodules compared to associated sediments (siliceous and calcareous). Major portion of Si, Al and K in both nodules and sediments appear to be of terrigenous nature. The elements which are highly enriched in the nodules compared to associated sediments from both siliceous and calcareous ooze are Mo – (307, 273), Ni – (71, 125), Mn – (64, 87), Cu – (43, 80), Co – (23, 75), Pb – (15, 24), Zn – (9, 11) and V – (8, 19) respectively. These high enrichment ratios of elements could be due to effective diagenetic supply of metals from the underlying sediment to the nodule. Enrichment ratios of transition metals and REEs in the nodule to sediment are higher in CIOB compared to Pacific and Atlantic Ocean. Nodule from red clay, exhibit very small enrichment ratio of four with Mn and Ce while, Al, Fe, Ti, Ca, Na, K, Mg, P, Zn, Co, V, Y and REE are all enriched in red clay compared to associated nodule. This is probably due to presence of abundant smectite, fish teeth, micronodules and phillipsite in the red clay. The strong positive correlation (r ? 0.8) of Mn with Ni, Cu, Zn and Mo and a convex pattern of shale-normalized REE pattern with positive Ce-anomaly of siliceous ooze could be due to presence of abundant manganese micronodules. None of the major trace and REE exhibits any type of inter-elemental relationship between nodule and sediment pairs. Therefore, it may not be appropriate to correlate elemental behaviour between these pairs.     

滇黔北坳陷五峰组-龙马溪组下段页岩岩相与沉积环境

滇黔北坳陷为南方海相地层的有利研究区域,发育多套海相页岩。上奥陶统五峰组与下志留统龙马溪组地层,尤其是五峰组-龙马溪组下段页岩作为优质烃源岩而备受重视。通过岩芯观察、薄片鉴定、X衍射分析及微量元素地球化学指标判识,对其进行页岩岩相划分与沉积环境分析。结果显示:滇黔北坳陷五峰组-龙马溪组下段地层共划分出六种页岩岩相:硅质页岩、黏土质页岩、钙质页岩、黏土质硅质混合页岩、黏土质钙质混合页岩、钙质硅质混合页岩,其中硅质页岩和黏土质页岩的TOC含量明显高于其余四种岩相。V/（V+Ni）、V/Cr、Ni/Co和U/Th指标指示五峰组-龙马溪组下段总体处于低能、滞留、局限条件,与深水陆棚环境匹配,Mo元素含量与四川盆地均值相当。五峰早期与龙马溪早期海侵的发生形成了以深水陆棚占主导的沉积格局,低能、滞留、局限的厌氧环境与快速海侵是有机质富集与保存的重要条件。     

Distribution and tectonic implications of Cretaceous-Quaternary sedimentary facies in Solomon Islands

Sedimentary rocks of the Solomon Islands-Bougainville Arc are described in terms of nine widespread facies. Four facies associations are recognised by grouping facies which developed in broadly similar sedimentary environments.A marine pelagic association of Early Cretaceous to Miocene rocks comprises three facies. Facies Al: Early Cretaceous siliceous mudstone, found only on Malaita, is interpreted as deep marine siliceous ooze. Facies A2: Early Cretaceous to Eocene limestone with chert, overlies the siliceous mudstone facies, and is widespread in the central and eastern Solomons. It represents lithified calcareous ooze. Facies A3: Oligocene to Miocene calcisiltite with thin tuffaceous beds, overlies Facies A2 in most areas, and also occurs in the western Solomons. This represents similar, but less lithified calcareous ooze, and the deposits of periodic andesitic volcanism.An open marine detrital association of Oligocene to Recent age occurs throughout the Solomons. This comprises two facies. Facies B1 is variably calcareous siltstone, of hemipelagic origin; and Facies B2 consists of volcanogenic clastic deposits, laid down from submarine mass flows.A third association, of shallow marine carbonates, ranges in age from Late Oligocene to Recent. Facies C1 is biohermal limestone, and Facies C2 is biostromal calcarenite.The fourth association comprises areally restricted Pliocene to Recent paralic detrital deposits. Facies D1 includes nearshore clastic sediments, and Facies D2 comprises alluvial sands and gravels.Pre-Oligocene pelagic sediments were deposited contemporaneously with, and subsequent to, the extrusion of oceanic tholeiite. Island arc volcanism commenced along the length of the Solomons during the Oligocene, and greatly influenced sedimentation. Thick volcaniclastic sequences were deposited from submarine mass flows, and shallow marine carbonates accumulated locally. Fine grained graded tuffaceous beds within the marine pelagic association are interpreted as products of this volcanism, suggesting that the Santa Isabel-Malaita-Ulawa area, where these beds are prevalent, was relatively close to the main Solomons chain at this time. A subduction zone may have dipped towards the northeast beneath this volcanic chain. Pliocene to Pleistocene calcalkaline volcanism and tectonism resulted in the emergence of all large islands and led to deposition of clastic and carbonate facies in paralic, shallow and deep marine environments.     

斯里兰卡普塔勒姆地区钙质结核的特征及成因

斯里兰卡国普塔勒姆地区滨海沉积物中发育钙质结核,其与我国黄海和东海钙质结核在成分、结构、构造和古生物化石等方面均存在差异。该地区钙质结核含有大量的海相生物化石及其碎屑,CaO的含量＞44.14％, SiO₂的含量＜12.75％,与同地区的碳酸盐软泥相比,结核相对富铁贫硅和富锶贫钡,说明生物对结核的影响大于对碳酸盐软泥的影响。结核的碳、氧同位素值负偏明显,δ¹³C＜-4.54‰,,δ¹⁸O＜-6.37‰,具有轻碳轻氧的特征。结核的矿物成分、古生物化石、主微量元素和碳、氧同位素资料说明其形成于海相环境,后期因海平面下降,受到大气淡水和地下水的影响,元素含量发生变化,形成颇具特色的钙质结核。     

Relationship between chemical composition and magnetic susceptibility in sediment cores from Central Indian Ocean Basin

Three sediment cores in a north-south transect (3°N to 13°S) from different sediment types of the Central Indian Ocean Basin (CIOB) are studied to understand the possible relationship between magnetic susceptibility (χ) and Al, Fe, Ti and Mn concentrations. The calcareous ooze core exhibit lowest χ (12.32 × 10⁻⁷ m³ kg⁻¹), Al (2.84%), Fe (1.63%) and Ti (0.14%), terrigenous clay core with moderate χ (29.93 × 10⁻⁷ m³ kg⁻¹) but highest Al (6.84%), Fe (5.20%) and Ti (0.44%), and siliceous ooze core with highest χ (38.06 × 10⁻⁷ m³ kg⁻¹) but moderate Al (4.49%), Fe (2.80%) and Ti (0.19%) contents. The distribution of χ and detrital proxy elements (Al, Fe, and Ti) are identical in both calcareous and siliceous ooze. Interestingly, in terrigenous core, the behaviour of χ is identical to only Ti content but not with Al and Fe suggesting possibility of Al and Fe having a non-detrital source. The occurrence of phillipsite in terrigenous clay is evident by the Al-K scatter plot where trend line intersects K axis at more than 50% of total K suggesting excess K in the form of phillipsite. Therefore, the presence of phillipsite might be responsible for negative correlation between χ and Al (r = −0.52). In siliceous ooze the strong positive correlations among χ, Al_exc and Fe_exc suggest the presence of authigenic Fe-rich smectite. High Mn content (0.5%) probably in the form of manganese micronodules is also contributing to χ in both calcareous and siliceous ooze but not in the terrigenous core where mean Mn content (0.1%) is similar to crustal abundance. Thus, χ systematically records the terrigenous variation in both the biogenic sediments but in terrigenous clay it indirectly suggests the presence of authigenic minerals.     

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）。