混合成因模式－－中国南方二叠一三叠系界线地层元素地球化学及其启示

含金云母和透辉石的纯橄岩呈浑圆状包体产于角闪闪长岩中。岩石组构、矿物成分和痕量元素等特征表明包体为上地幔成因,并且为地幔橄榄岩高度部分熔融的残留体。包体和寄主岩的微量元素研究表明,岩浆源区为富集型地幔,部分熔融之前曾发育有不相容元素的富集作用——地幔交代作用。     

青藏高原东南木里地区二叠纪苦橄岩的Os-Sr-Nd同位素地球化学研究

本文报道了在青藏高原东南木里地区发现的二叠纪苦橄岩和与其共生玄武岩的主微量元素地球化学特征以及Os-Sr-Nd同位素组成。苦橄岩和与其共生玄武岩受地壳混染作用影响较小。根据苦橄岩的Ti/Y比值和初始的Os同位素组成,将木里苦橄岩分为两类:高Ti/Y型苦橄岩和低Ti/Y型苦橄岩,其中高Ti/Y型苦橄岩具有高的γ_(Os)= 5.3～ 10.7和ε_(Nd)= 5.9～ 6.4,与全球典型洋岛玄武岩的Os和Nd同位素组成接近,代表了地幔柱源区的同位素特征;而低Ti/Y型苦橄岩具有低的γ_(Os)=-4.1～ 1.2和ε_(Nd)= 3.2～ 5.0,可能表明受到了SCLM(大陆岩石圈地幔)源区物质的混染。与其共生的玄武岩具有低的γ_(Os)=-3.5～-1.6和ε_(Nd)=-0.6～ 0.7,表明其来自于不同于低Ti/Y型苦橄岩也有异于高Ti/Y型苦橄岩的地幔源区,但是也可能受到了SCLM物质的混染。基于Nd-Os同位素的地幔柱与SCLM的二端元混合模型显示:低Ti/Y型苦橄岩可能是SCLM物质组分与地幔柱起源的苦橄质原始岩浆混合形成的;与苦橄岩共生的玄武岩可能是由地幔柱来源的玄武质岩浆与SCLM小比例熔融的熔体混合形成的。     

广东普宁麒麟辉石岩幔源包体的矿物学特征及其形成条件

广东普宁麒麟起镁铁岩集块角砾岩筒中,含有大量的二辉橄揽岩-方辉橄揽岩、辉石岩幔源包体。辉石岩包体共有三种类型:尖晶石单辉岩、石榴石单辉岩和二辉岩,其岩石学、岩石化学及微量元素特征的研究已另文发表。本文主要研究该区辉石岩包体的矿物学特征,以及对其形     

金在地幔矿物中的赋存形式及其赋存介质转化的可能模式:以中国北方一些地幔橄榄岩包体为例

采集中国北方玄武岩中橄榄岩包体样品21件。测定了其中的主元素、微量元素、稀土元素(REE)和Au等的含量。橄榄岩包体中的Au含量与CaO含量的相关性表明,其中的Au可能主要赋存于单斜辉石中,反映Au含量可能与地幔演化及熔融程度有关;橄榄岩包体后期受地幔流体交代作用的影响,Au转而以硫化物形式存在,这一过程是在橄榄岩包体原有Au的物质基础上进行的。     

滇西六合正长斑岩和花岗岩包体中锆石U-Pb年代和微量元素地球化学研究

六合正长斑岩是滇西新生代富碱斑岩的典型代表,以发育各类深浅不一的岩石包体而闻名,其中包括了同期的花岗岩包体;主岩和包体所蕴含的深部地质过程对于富碱岩浆的形成和演化具有重要约束作用。本文以六合正长斑岩和其中花岗岩包体的锆石微量元素地球化学为研究重点,结合主岩主量元素、锆石U-Pb年龄、Ti温度、锆石氧逸度的对比研究,分析和探讨富碱岩浆的形成和演化过程。研究表明:锆石U-Pb年龄所限定的六合富碱岩浆活动时限为(37.89±0.96)~(35.87±0.58) Ma;而花岗岩包体代表的同期富硅酸性岩浆活动时限为(38.21±0.44)~(36.21±0.36) Ma;两者几乎同步活动。锆石微量元素成因判别图显示主岩锆石主要位于钾镁煌斑岩范围,暗示富碱岩浆源区具地幔属性;花岗岩包体锆石大多位于花岗岩范围,两者在花岗岩范围有部分重叠,证实了主岩锆石和花岗岩包体锆石结晶时存在共同的生长环境。Ce^(Ⅳ)/Ce^(Ⅲ)比值估算和Ti温度计算显示,在36.42~36.41 Ma范围内富碱岩浆氧逸度和锆石结晶温度发生突变,指示在该时限内富碱岩浆及所裹挟的花岗质岩浆发生了混合作用;氧逸度的振荡降低反映了后期幔源岩浆的补充。综合研究认为,六合地区来自富集地幔的喜山期富碱岩浆底侵熔化上覆深部地壳长英质岩石形成花岗质岩浆,随即以富碱岩浆为主与少量花岗质岩浆不均一混合并同步结晶成岩形成含有花岗岩包体的正长斑岩。     

西藏松多榴辉岩的矿物原位微量元素地球化学研究

对松多榴辉岩中单矿物进行的LA-ICP-MS原位微区微量元素分析研究结果表明,石榴石主要富集中、重稀土元素和Y,同时具有高丰度的Sc、V、Cr和Co等元素;绿辉石中的微量元素以中稀土元素、Sr、Sc、V、Cr、Co、Ni和Ti为主,含有一定量的Zr、Hf等。石榴石、绿辉石、角闪石和绿帘石中均显示轻稀土元素亏损的特点,表明在退变质过程中没有发生明显的富轻稀土元素的外来流体交代作用,因而其微量元素矿物地球化学的某些特点不同于苏鲁地区的榴辉岩。石榴石变斑晶中某些元素(如Ti、Zr)的分带性暗示了榴辉岩在紧随峰期变质之后的折返过程中发生了降压增温过程。榴辉岩主要变质矿物中微量元素的分配显然受到矿物主量元素的分配所控制,如MgO在石榴石和绿辉石之间的分配对Ni、Co、Ti分配的控制以及CaO的分配对Sr、Y、REE分配的控制等。退变质过程中矿物的形成或分解以及物理化学条件的改变都可以引起矿物间微量元素的重新分配。由绿辉石退变质而形成的角闪石,较之原先的绿辉石,其微量元素配分曲线总体特征会发生变化,但元素总体丰度相近,某些元素特点相似,又反映了绿辉石和角闪石之间的成生联系。金红石是Ti、Nb、Ta、Zr、Hf的主要赋存矿物,而与之共生的绿帘石所表现出来的高场强元素的亏损特征表明了金红石的存在所带来的影响。     

Ag在橄榄石、斜方辉石、单斜辉石和玄武质熔体间的分配

地幔部分熔融过程中亲S元素Ag的分配行为能够限定地幔中Ag含量,同时可以追踪地幔中S含量和去向。在地幔部分熔融过程中, Ag的分配行为与其在地幔硅酸盐矿物–玄武质熔体间的分配系数密切相关。因此准确地测定Ag在除硫化物之外地幔硅酸盐矿物和共存熔体之间的分配系数是预测Ag分配行为的必要条件之一。目前缺乏Ag在地幔矿物(橄榄石、辉石等)和玄武质熔体之间分配系数的报道,阻碍了对Ag在地幔部分熔融过程中分配行为的研究。本研究通过高温高压实验获得了在洋中脊玄武岩(MORB)产生的温度和压力条件下,Ag在橄榄石(ol)、斜方辉石(opx)、单斜辉石(cpx)与玄武质熔体(melt)之间的分配系数,分别为D_Ag^ol/melt=0.0005±0.0002、D_Ag^opx/melt=0.007±0.003和D_Ag^cpx/melt=0.046±0.009。根据实验获得的分配系数进行模拟的计算结果表明,太古代科马提岩和洋中脊苦橄岩源区的地幔Ag含量为(8±2)×10-9。如果这个值...     

阿尔金环形山榴辉岩岩石地球化学及地质意义

调查研究发现,阿尔金南缘环形山榴辉岩呈透镜体状产于新元古代石榴石二长花岗片麻岩中,岩石经退变质作用,白眼圈构造发育,石榴石变少,石英及金红石等矿物较少,未见峰期矿物组合。绿辉石被次透辉石及角闪石替代,岩石为榴辉岩、榴闪岩及斜长角闪岩。主量及微量元素地球化学分析显示:主量元素Al2O3、TiO2、MgO、P2O5及稀土Nb/Ta、Zr/Hf、Zr/Nb、La/Nb、Y/Nb特征比值与洋脊玄武岩一致;稀土标准化模式图、微量元素原始地幔标准化图及MORB标准化图指示岩石具洋脊玄武岩特征,原岩可能为地幔岩经15%~30%的部分熔融形成。结合榴辉岩围岩年龄、变质作用等分析认为,该榴辉岩为似洋脊玄武岩的基性岩浆侵入花岗岩后,于500 Ma左右发生大陆俯冲折返形成。     

云南中甸峨眉山玄武岩中超基性－基性岩包体元素地球化学分析

峨眉山大火成岩省于滇西地区广泛发育有一系列的镁铁-超镁铁质岩体,但对于其中地幔包体的报道还相对较少。本次研究在云南中甸地区峨眉山玄武岩中发现了岩性表现为由纯橄岩→辉橄岩→橄辉岩→苦橄岩→辉长岩→辉绿辉长岩→辉绿岩变化系列的超基性-基性岩包体。通过对包体岩石开展元素地球化学分析研究,结果表明:形成包体的原始超基性岩浆属于峨眉山地幔柱活动产物,且与主岩形成背景相似,其岩浆源区位于难熔的方辉橄榄岩区与石榴二辉橄榄岩区的过渡部位,受岩石圈地壳混染程度较低。结合丽江苦橄岩性质,认为滇西地区上地幔存在早阶段峨眉山地幔柱活动。     

新疆坡北镁铁-超镁铁质岩体地球动力学背景探讨

坡北镁铁-超镁铁质岩体位于塔里木板块东北缘的北山地区,主要由坡一、坡三、坡七和坡十等十几个侵入体组成,已发现坡一和坡十岩体赋存大型Cu-Ni硫化物矿床,目前对坡北含矿岩体成岩成矿构造背景存在不同认识。本文对坡一岩体各类岩石的矿物、主量和微量元素组成进行了系统分析,坡北岩体橄榄石Fo值范围为83.17～90.2,斜方辉石主要为古铜辉石,单斜辉石主要为普通辉石和透辉石;铬尖晶石Cr^#和Mg^#值变化范围分别为0.45～0.69和0.11～0.41,具有由富铝、富镁向富铬、富铁方向演化的趋势。微量元素具有明显的Nb、Ta和Ti负异常,Pb正异常。岩体主量元素变化特征主要受橄榄石、辉石和斜长石分离结晶/堆晶作用控制。模拟计算表明,岩体母岩浆MgO含量为16.09%,FeO含量为10.38%,岩浆结晶温度为1 331～1 411℃,为高温苦橄质岩浆。坡北岩体是早期受俯冲流体交代的岩石圈地幔在塔里木地幔柱作用下发生较高程度部分熔融的产物。     

橄榄石微量元素原位分析的现状及其应用

随着高精度EMPA和LA-ICP-MS分析技术的发展和矿物微量元素测试精度的提高,利用橄榄石中的微量元素示踪地幔部分熔融、地幔交代作用、岩浆早期结晶过程等地质问题成为近年来一个新兴的研究方向。一系列开拓性的研究发现也被陆续的发表,主要涉及橄榄石中Ni、Co、Al、Cr、Zn、Ti、Li、V、Sc、Mn、Ca和P等元素的示踪使用。一些卓有成效的示踪方法为:Ca、Al、Ti、Ni及Mn能够很好的用于区分橄榄石捕掳晶和斑晶;橄榄石-尖晶石地幔演化趋势线(OSMA:olivine-spinel mantle array)图解可以用于表征岩浆源区的亏损程度;玄武岩中橄榄石斑晶的Li同位素及Li含量可以很有效地指示岩浆源区是否存在地壳物质再循环及地幔交代作用;橄榄石斑晶中Ni、Ca、Mn、Cr和Al协变关系图解可以识别岩浆的辉石岩源区;利用橄榄石捕掳晶中Zr和Sc的含量差异特征可将橄榄岩中三种最主要的类型(尖晶石橄榄岩、石榴石橄榄岩以及尖晶石-石榴石橄榄岩)区分开来;一些元素的比值或组合(例如Ni/Co、Fe/Mn、V/Sc、Zr和Sc、Ca和Ti)可以指示源区交代作用、岩浆作用过程及氧化状态;基于橄榄石中Al、Cr及Ca的地质温度计可以为推算地幔热状态提供新方法;基于橄榄石分离结晶Fo-NiO演化线的原始岩浆计算模型可以较好的推算原始岩浆成分;利用橄榄石的环带及微量元素的扩散机制可以判别更多岩石成因信息,如识别交代介质、熔体类型以及地质构造背景等。基于上述最新研究的相关资料和已有成果,本文对橄榄石微量元素的地球化学示踪方法做系统性的归纳整理,并对橄榄石微量元素赋存状况、橄榄石微量元素测试方法、橄榄石微量元素的使用条件及需注意的问题等进行讨论,为读者在做相关研究时提供参考。     

金川超大型Ni-Cu-(PGE)矿床橄榄石微量元素特征及地质意义

我国金川超大型铜镍硫化物矿床是世界上第三大在采岩浆硫化物矿床,Ni开采量仅次于俄罗斯Noril'sk-Talnakh和加拿大Sudbury矿床,其成因研究备受关注。利用激光—等离子体质谱(LA-ICP-MS)原位分析了金川岩体中橄榄石微量元素含量,并探讨了影响元素含量变化的因素,进而阐述成岩及成矿过程。分析结果显示橄榄石中元素Ni,Cr与Fo呈负相关,Mn/Fe与Fo呈正相关,而Mn/Zn,Zn/Fe与Fo无相关性。在原始地幔橄榄石多元素标准化图中,金川Ⅰ号和Ⅱ号岩体橄榄石具相同的配分模式,均显示Cr,V,Ni,Co和Ti的亏损,富集不相容元素Zr,Y,Ti,Sc和Ca的特征。元素变化特征暗示Ⅰ号和Ⅱ号岩体具相同的母岩浆成分;与铬尖晶石的共结使橄榄石亏损Cr,V和Ti元素,而熔离的硫化物及其与橄榄石的相互反应共同影响着橄榄石中Ni和Co元素的含量。Ⅱ号岩体橄榄石较Ⅰ号岩体具较低的Cr和V含量,暗示Ⅱ号岩体母岩浆较Ⅰ号岩体经历了更高程度的演化。橄榄石高的Mn/Zn值(>13)和低的Zn/Fe值(<11)指示金川岩体岩浆可能起源于橄榄岩地幔的部分熔融,而非辉石岩地幔源区。     

Trace Elements in Olivines from the Giant Jinchuan Ni-Cu-(PGE) Deposit,NW China,and Its Geological Implication

The giant Jinchuan magmatic sulfide deposit in China is the third largest mining deposits in the world. Although many research have been done, there still exist some debates in the genesis of deposit. This study using the LA-IC-MS to obtain the trace elements concentrations of the olivine in order to discuss the mechanism of influence the element variability and illustrate the process of magmatism and ore-forming. The analytical results show that Ni, Co correlate negatively with Fo in the olivine, Mn/Fe is positively correlate with Fo, while Mn/Zn and Zn/Fe show no obvious correlation with Fo. The primitive mantle olivine-normalized trace element patterns of the Jinchuan olivine show that Jinchuan Ⅰ, Ⅱ intrusions have the same trace elements characteristics, which display negative Cr, V, Ni, Co and Ti anomalies and enrichment of Zr, Y, Ti, Sc and Ca. The multi-element patterns of the Jinchuan olivine imply same parental magma in the intrusion Ⅰ and Ⅱ. The spinel which cocrystallization with the olivine make it display negative Cr, V and Ti anomalies. The contents of Ni and Co in olivine are influenced by the process of sulfide segregation and the reaction between sulfide and olivine. The lower content of Cr and V in olivine of the intrusion Ⅱ compared with the intrusion Ⅰ imply that the parental magma of the intrusion Ⅱ was more evolved. Higher Mn/Zn (>13) ratios and lower Zn/Fe (<11) ratios indicate that the magma of Jinchuan intrusion likely originate from partial melting of peridotite mantle possibly, instead of pyroxene mantle sources.     

Mineral and inorganic chemical composition of the Pernik coal, Bulgaria

The mineral and inorganic chemical composition of five types of samples from the Pernik subbituminous coals and their products generated from the Pernik preparation plant were studied. They include feed coal, low-grade coal, high-grade coal, coal slime, and host rock. The mineral matter of the coals contains 44 species that belong mainly to silicates, carbonates, sulphates, sulphides, and oxides/hydroxides, and to a lesser extent, chlorides, biogenic minerals, and organic minerals. The detrital minerals are quartz, kaolinite, micas, feldspars, magnetite, cristobalite, spessartine, and amphibole. The authigenic minerals include various sulphides, silicates, oxihydroxides, sulphates, and carbonates. Several stages and substages of formation were identified during the syngenetic and epigenetic mineral precipitations of these coals. The authigenic minerals show the greatest diversity of mineral species as the epigenetic mineralization (mostly sulphides, carbonates, and sulphates) dominates qualitatively and quantitatively. The epigenetic mineralization was a result of complex processes occurring mostly during the late development of the Pernik basin. These processes indicate intensive tectonic, hydrothermal and volcanic activities accompanied by a change from fresh to marine sedimentation environment. Thermally altered organic matter due to some of the above processes was also identified in the basin. Most of the trace elements in the Pernik coals (Mo, Be, S, Zr, Y, Cl, Ba, Sc, Ga, Ag, V, P, Br, Ni, Co, Pb, Ca, and Ti) show an affinity to OM and phases intimately associated with OM. Some of the trace elements (Sr, Ti, Mn, Ba, Pb, Cu, Zn, Co, Cr, Ni, As, Ag, Yb, Sn, Ga, Ge, etc.) are impurities in authigenic and accessory minerals, while other trace elements (La, Ba, Cu, Ce, Sb, Bi, Zn, Pb, Cd, Nd, etc.) occur as discrete phases. Elements such as Sc, Be, Y, Ba, V, Zr, S, Mo, Ti, and Ga exceed Clarke concentrations in all of the coal types studied. It was also found that a number of elements in the Pernik coals (F, V, As, Pb, Mo, Li, Sr, Ti, Ga, Ni, Ge, Cr, Mn, etc.) reveal mobility in water and could have some environmental concerns.     

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）。     

Residence of trace elements in metasomatized spinel lherzolite xenoliths: a proton-microprobe study

Minerals occurring in dry and modally metasomatized spinel lherzolites from western Victoria have been analysed by proton microprobe for Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Ba, Pb, Br, rare-earth elements (REE), Th and U. Mass-balance calculations demonstrate that these trace elements are contained in specific acceptor minerals and do not occur in significant concentrations at clean grain boundaries. The level of particular trace elements in the rock depends on the presence of specific phases: for example high levels of REE, Sr (and U, Th, Br) require apatite, while Ba, Nb and Ta are strongly concentrated in amphibole±mica. Mantle metasomatism in these spinel lherzolites is inferred to result from an open-system process involving infiltration of fluids released by crystallizing silicate melts. This process produces metasomatic zones with different modal mineralogy and hence greatly different trace-element signatures. The data demonstrate that large-ion-lithophile (LIL) and high-field strength (HFS) elements in metasomatized spinel lherzolites are strongly concentrated in non-refractory phases, which will break down easily in heated volumes such as the walls of magma conduits. The heterogeneity observed in trace-element patterns of intraplate alkali basaltic rocks may not reflect source heterogeneity, but may result largely from contamination by metasomatized mantle wall rock. The K_Ds for most trace elements show little temperature dependence except for K_DSr between orthopyroxene and clinopyroxene where K_D decreases with increasing temperature. The generally uniform K_Ds can be used to test for disequilibrium in such assemblages.     

华北地块东南缘中生代侵入杂岩中所含榴辉岩类包体矿物微量元素地球化学特征及其意义

华北地块东南缘中生代侵入杂岩中所含榴辉岩类包体中矿物的分析结果表明, 组成榴辉岩类包体的各矿物之间元素的分配在榴辉岩相变质阶段已经达到了化学平衡;石榴石中Al、Fe、Mn, 单斜辉石中Na、Mg、Ca, 角闪石中Na、Mg、Fe等主量元素含量与其全岩之间均呈良好的正相关, 受全岩成分制约;石榴石明显富集HREE、贫LREE, 单斜辉石相对富集LREE、MREE、贫HREE, 两者轻、重稀土含量呈相互消长的互补关系, 石榴石和单斜辉石中分别富集Y、Sr, Ga和过渡族元素Sc、Ti、V、Cr、Co等含量较高, 其含量受全岩成分控制;金红石中稀土元素的含量很少, Fe、Al、Mg、Ca、Mn、Nb、Ta、Cr和Zr含量相对较高, Rb、Sr、Ba含量极低, 部分微量元素(如Nb、Cr、Fe、V、W等)含量与其原岩有继承和对应关系;部分原生或/和退变角闪石的REE配分模式分别与单斜辉石和石榴石相似, 过渡族金属元素等的含量与石榴石、单斜辉石和全岩具有一定的相关性, 角闪石容纳Na、K、Sr、Rb、Ba等元素的能力较强, 其成分除受全岩成分的制约外, 石榴石、单斜辉石对其形成也有影响。榴辉岩类包体与其寄主中生代侵入杂岩中部分高价态/高场强元素(HFSE)和重稀土元素(HREE)呈相互消长的关系。榴辉岩的形成与扬子地块和华北地块之间的俯冲-碰撞作用有关。     

Melting and metasomatism in the continental lithosphere: laser ablation ICPMS analysis of minerals in spinel lherzolites from eastern Australia

Olivine, low-Ca pyroxene, diopside, and spinel from a suite of protogranular lherzolite xenoliths from southeastern Australia have been analysed for their major and trace element compositions using electron microprobe and laser ablation ICPMS. Bulk compositions of the lherzolites range from fertile (12–13% modal diopside) to depleted (2–3% modal diopside), with equilibration temperatures of 850–900 °C indicating entrainment of these lherzolites from relatively shallow depths (probably ≤ 35 km) within the lithosphere. Mineral compositions and abundances indicate a primary control by partial melting, with decreasing abundance of modal diopside accompanied by increasing Mg# of olivine and pyroxene, decreasing Al and Ti contents of diopside, increasing Ni contents of olivine, and increasing Cr/Al of spinel. HREE, Y, and Ga in diopside also follow melting trends, decreasing in concentration with increasing Mg#. In contrast, highly incompatible elements such as LREE, Nb, and Th reveal divergent behaviour that cannot be ascribed entirely to partial melting. Diopsides from the fertile lherzolites have mantle-normalized patterns that are depleted in Th, Nb, and the LREE relative to Y and the HREE, whereas, diopsides from the cpx-poor samples are strongly enriched in Th, Nb and the LREE, and have elevated Sm/Hf and Zr/Hf, and low Ti/Nb. All diopsides have strongly negative Nb anomalies relative to Th and the LREE. Trace element patterns of diopside in the fertile lherzolites can be reproduced by ≤ 5% batch melting of a primitive source. The negative Nb anomalies are a consequence of this melting, and do not require special conditions or tectonic environments. The low concentrations of Y and HREE in diopside from the cpx-poor lherzolites cannot be produced by realistic degrees of batch melting, but can be accomplished by up to ∼20% fractional melting, suggesting multiple episodes of melt depletion. Os isotopic compositions of these lherzolites show that the melt depletion events occurred in the middle and late Proterozoic, demonstrating the long-term stability of lithospheric mantle beneath regions of eastern Australia. The LREE-enriched diopsides are well equilibrated and record metasomatic enrichment events that pre-date the magmatism that entrained these xenoliths. Trace element patterns of these pyroxenes suggest a carbonatitic melt as the metasomatic agent. Received: 24 September 1996 / Accepted: 12 August 1997     

Specific chemical and mineral composition of ferromanganese nodules from the Chukchi Sea

The specific chemical and mineral composition of discoid, cake-shaped, and platy ferromanganese nodules (FMNs) from the Chukchi Sea are considered. The main ore components of these FMNs are Fe, Mn, and P. The contents of trace elements (except for Ba and Sr) do not exceed hundredths of percent. Maximum concentrations of most of these elements are specific for the cake-shaped nodules. In general, Mn accumulates most intensely in FMNs. Next (in order of decrease) are Ag(?), Co, and Pb; Sr, Fe, P, Y, and Ca; and Ni, La, Zn, and Cu. As for Ba, Cr, Mg, and K, they do not accumulate in the FMNs. “Dilution” is typical of Si, Al, Na, and Ti. The main ore phases are strengite and amorphous Mn hydroxides. It has been revealed for the first time for the Chukchi Sea that Cu, Zn, Sn, Ni, Pb, W, Bi, Cr, Fe, Ti, Ag, Au, Y, Zr, and La–Nd lanthanides form individual mineral microphases in FMNs: native elements, intermetallic compounds, oxides, and, much more seldom, tungstates, silicates, and phosphates. Accessory ore mineralization is the best pronounced and most diverse in the platy nodules. Though the FMNs from the Chukchi Sea are diagenetic, high-temperature fluids are, most likely, the source of microinclusions of various accessory ore minerals.     

松嫩平原西部碱尘气溶胶的元素特征分析

碱尘暴期间松嫩平原西部碱尘气溶胶的主要元素质量浓度排序为Na、Al、Fe、Ca、Mg、K、Ti、Ba、Zn,与当地盐碱化土壤的元素组成吻合,而与沙尘、城市气溶胶的元素组成有差别。风力对碱尘气溶胶元素组成有明显的影响,当风速在8.0~17.1 m/s时,元素组成的质量浓度排序为Na、Ca、Al、Fe、Mg、K、Ba、Ti、Zn。Na元素质量浓度的激增是碱尘暴元素组分的一大特征,明显富集元素为Na和B;相对于当地背景大气气溶胶的富集情况,Zn、Cu、Ba、B的富集因子值在碱尘暴期间明显降低;在各种天气情况下,B、Cu均具有较高的富集因子。碱尘中Ti元素的富集因子值均小于1,而Ca、Fe、K、Mg、Mn、Sr、V的富集因子值为1~4。两个采样点的Ca、Na、Al、Fe、Mg、Ti、Zn的富集因子近似,表明该区碱尘的主要元素具有特定的一致性;而B、Ba、Cu、V的富集因子相差较大,可以作为区分不同碱尘源的标志性元素。