Geochemistry of the Apulian karst bauxites (southern Italy): Chemical fractionation and parental affinities

This study focuses on a late Cretaceous karst bauxite deposit in the Murge area of the Apulia district, southern Italy. The first analysis of the vertical distributions of a wide range of elements (including REEs and selected trace elements) throughout the deposit was shown in order to identify the processes determining element fractionation during the evolution of the bauxite.The studied karst bauxite deposit exhibits an ooidal texture, is mineralogically homogeneous, and contains higher abundances of boehmite than of hematite, kaolinite, and anatase. The major element composition of the bauxite is dominated by elevated concentrations of SiO₂, TiO₂, Al₂O₃, and Fe₂O₃, and analyses of element mobility within the bauxite indicate that all elements except for Nb and Ni, and to a lesser extent Cr, are depleted relative to the immobile element Ti. R-mode factor analysis revealed a number of key findings: (i) some low-solubility elements (e.g., Zr, Th, Ti, V, Ga) were concentrated in detrital zircon and monazite (Zr, Th), in anatase (Ti, V), and possibly in boehmite and hematite (Ga) during the later stages of bauxitisation; (ii) Fe and Cr were concentrated during wet conditions, whereas Al and Co accumulated during dry conditions; (iii) distributions of the light REEs (LREEs) and the heavy REEs (HREEs) are controlled by the same processes, suggesting that little LREE/HREE fractionation occurred during bauxite formation; and (iv) the behaviour of cerium is different from that of the other REEs, and highly variable cerium anomalies are observed across the deposit, with three characteristic Ce/Ce* maxima with values of > 2. Parisite was the only authigenic cerium mineral detected during this study. Thus, we propose a three-step model to explain the distribution of Ce: cerianite is dissolved by cerium reduction, is transported by downward-moving meteoric water (per descensum), and finally parisite is precipitated. This cycle was repeated several times in the Apulian karst bauxite in response to Eh decreases under alkaline conditions, promoted by fluctuations in the groundwater level. Finally, we used the value of the Eu anomaly to discuss the parental affinity or protolith of the bauxite. The value of the Eu anomaly (min. Eu/Eu* = 0.76, max. Eu/Eu* = 0.89) indicates that the bauxite was not derived from carbonates, but rather, that the majority of the bauxite was influenced by intermediate to mafic magmatic sources. Eu/Eu* vs Sm/Nd diagram suggests that the parental material for the bauxite was derived from a combination of a distant magmatic source and clastic material derived from a continental margin (northern Africa) to the south.     

Origin and geochemical evolution from ferrallitized clays to karst bauxite: An example from the Lower Cretaceous of NE Spain

Four outcrops of Lower Cretaceous (Barremian) karst bauxites located in Teruel (NE Spain) were analysed. The deposits show a heterogeneous-chaotic lithostructure consisting of pisolitic bauxite blocks embedded in lateritic red clays filling karst cavities. The research has focused on the geochemical study of major, minor, and trace elements (including some critical to industry) of both the bauxites and clays. The objective was to investigate the bauxite precursor material and to characterize the system’s geochemical evolution. Geochemical analyses were carried out by inductively-coupled plasma optical emission and mass spectroscopy. An absolute weathering index has been calculated to estimate element mobility, assuming Ti as an immobile element and the Upper Continental Crust (UCC) as parent material. Further, selected samples were observed by field emission scanning electron microscopy. The data indicate that both the bauxites and red clays originated by intense chemical weathering from more mafic argillaceous sediments than the UCC. Ongoing weathering caused the bauxitization of the upper parts of the original profile, preventing the lower parts from being bauxitized, thus producing the ferrallitized clays underlying the pisolitic bauxites. Subsequent karst reactivation gave rise to the current lithostructure. Ferrallitization is related to Fe, Sc, and V enrichment. On the other hand, although bauxites are relatively enriched in some elements compared to clays, the more intense chemical weathering associated with bauxitization led to chemical homogenization and widespread element depletion. During the bauxitization, Al, Ti, Zr, Cr, and probably Hf and the critical element Nb behaved as more immobile elements in the system. Bauxitization also enhanced homogenization and depletion of the REE, which is more pronounced for the LREE. HREE trends seem to be partly related to the concentration of Ti oxides in the bauxites, whereas P-bearing phases, more frequent in the clays, control the LREE. Subsequent to bauxitization, partial kaolinization of the bauxite took place related to the circulation of acid solutions that also caused the karst reactivation. These late processes caused some Al depletion in the bauxites and enhanced Fe loss together with V and, to a lesser extent, Ge.     

Concentration distribution and assessment of several heavy metals in sediments of west-four Pearl River Estuary

Grain size parameters, trace metals (Co, Cu, Ni, Pb, Cr, Zn, Ba, Zr and Sr) and total organic matter (TOM) of 38 surficial sediments and a sediment core of west-four Pearl River Estuary region were analyzed. The spacial distribution and the transportation procession of the chemical element in surficial sediments were studied mainly. Multivariate statistics are used to analyses the interrelationship of metal elements, TOM and the grain size parameters. The results demonstrated that terrigenous sediment taken by the rivers are main sources of the trace metal elements and TOM, and the lithology of parent material is a dominating factor controlling the trace metal composition in the surficial sediment. In addition, the hydrodynamic condition and landform are the dominating factors controlling the large-scale distribution, while the anthropogenic input in the coastal area alters the regional distribution of heavy metal elements Co, Cu, Ni, Pb, Cr and Zn. The enrichment factor (EF) analysis was used for the differentiation of the metal source between anthropogenic and naturally occurring, and for the assessment of the anthropogenic influence, the deeper layer content of heavy metals were calculated as the background values and Zr was chosen as the reference element for Co, Cu, Ni, Pb, Cr and Zn. The result indicate prevalent enrichment of Co, Cu, Ni, Pb and Cr, and the contamination of Pb is most obvious, further more, the peculiar high EF value sites of Zn and Pb probably suggest point source input.     

Source and distribution of metals in urban soil of Bombay,India, using multivariate statistical techniques

Simplification of a complex system of geochemical variables obtained from the soils of an industrialized area of Bombay is attempted by means of R-mode factor analysis. Prior to factor analysis, discriminant analysis was carried out taking rock and soil chemical data to establish the anthropogenic contribution of metals in soil. Trace elements (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn) are expressed in terms of three rotated factors. The factors mostly indicate anthropogenic sources of metals such as atmospheric fallout, emission from different industrial chimneys, crushing operations in quarries, and sewage sludges. Major elements (Na, Mg, Al, Si, P, K, Ca, Ti, Mn, and Fe) are also expressed in terms of three rotated factors indicating natural processes such as chemical weathering, presence of clay minerals, and contribution from sewage sludges and municipal refuse. Summary statistics (mean, standard deviation, skewness, and kurtosis) for the particle size distribution were interpreted as moderate dominance of fine particles. Mineralogical studies revealed the presence of montmorillonite, kaolinite, and illite types of clay minerals. Thus the present study provides information about the metal content entering into the soil and their level, sources, and distribution in the area.     

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。     

Trace-element content of “Karst Bauxites” and their parent rocks in the mediterranean belt

This work deals with a concise but comprehensive study of trace-element distribution in the bauxite deposits of Mediterranean belt. Although the alloctonous and mainly detritic characters of several “karst bauxite” deposits are well established, their parent rock has remained largely enigmatic. Evidence is available that some chemical elements, notably Zr, Cr and Ga are largely immobile during the weathering and diagenesis and study of such trace-elements in “karst bauxites” permits to make an approach to the lithological nature of their parent rocks. It is shown, by reference to analyses of bauxites from Mediterranean areas, that all the deposits studied are aligned from a Cr rich pole related to ultramafics to another pole rich in Ga and Zr contents and in genetical relation with acidic parent rocks. The results obtained by this way have been controlled by application of “trace-element accumulation coefficient” which permits to distinguish four principal zones of bauxite derived from the parent rock of different lithological characters (Fig. 3).     

Trace-element distribution and ore formation in vein-metasomatised peridotite at Kalskaret,near Tafjord,South Norway

The concentration profiles of the trace elements, S, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Sr, and Y have been determined across a metasomatic vein in peridotite. The introduced elements Ti, V, Sr, and Y show specific enrichment in particular silicate phases in accordance with the availability of suitable lattice sites. In contrast, the other introduced trace elements (Cu and S) behave more like the redistributed elements, Cr, Ni, Mn, and Co which do not show concentration ‘fronts’ that can be simply related to the silicate minerals. Concentration of pentlandite, chalcopyrite, and Cr-magnetite near the boundary between the enstatite and anthophyllite zones gives rise to maxima in the Ni, Cu, S, and Cr distributions, while in the chlorite zone significant concentrations of Cr and Ni occur in the chlorite itself. Control of the distribution of Ni, Cu, and Cr is ascribed to the oxidation/reduction reactions involved in the formation of pentlandite, chalcopyrite and Cr-magnetite, together with the critical role of Al in limiting chlorite formation during metasomatism.     

桂西田阳堆积型铝土矿矿物学及地球化学

[摘 要]桂西田阳堆积型铝土矿产于第四纪红土层中。本文通过对桂西田阳第四系堆积型铝土矿进行一系列矿物学与地球化学研究,探索铝土矿的物质来源。矿物学分析显示铝土矿石中主要矿物为硬水铝石、赤铁矿和锐钛矿,含有少量高岭石、鲕绿泥石、三水铝石、针铁矿、金红石、伊利石、蒙脱石和石英等。地球化学分析显示,组成铝土矿石的主要化学组分有Al₂O₃、Fe₂O₃、SiO₂、TiO₂、FeO 和H₂O⁺;微量元素分析显示,铝土矿石相对地壳和原始地幔富集B、Li、Ga、Zr、Hf、Nb、Ta、W、Th、U 等元素,而亏损Ni、Cr 等元素。矿石中明显富集稀土元素,稀土总量变化大,轻重稀土分异明显,轻稀土元素富集明显;矿石具有明显的铈异常和铕异常,且铕异常相对稳定,为一致的负异常。元素相关性分析显示常量元素间相关性较差;部分微量元素如Zr、Hf、Nb 和Ta 间呈现出较高的正相关性。通过Zr/ Hf、Nb/ Ta 图解、Eu/ Eu* - TiO₂/ Al₂O₃图解和Zr-Cr-Ga 图解综合分析显示铝土矿物质来源复杂,底板碳酸盐岩和周围火成岩都为铝土矿提供物源。     

Geochemistry of the apulian allochthonous karst bauxite,Southern Italy: Distribution of critical elements and constraints on Late Cretaceous Peri-Tethyan palaeogeography

A comprehensive study of pebbles from the 'Salento-type' allochthnous bauxite deposit (Otranto, southern Italy), originally derived from a pristine Campanian bauxite, has been performed for evaluating: 1) the chemical fractionation and inter-elemental relationships, especially for critical elements, 2) the climatic conditions that promoted bauxite formation, and 3) the provenance of the protolith(s) using zircon age data and conservative elemental proxies. The study confirms the capability of bauxite to concentrate many elements defined as critical by the European Union report on critical raw materials. Sc, Co, Ga, and especially Cr, are enriched when compared with the UCC composition and assuming Nb is immobile. Other critical elements such as the REEs, with the exception of La, are moderately depleted. R-mode factor analysis suggests that most of the variance in our chemical dataset is explained by a factor with significant weightings for TiO₂, Al₂O₃, Fe₂O₃, Sc, V, Nb, REEs, Pb and Th. This arises from climate effects affecting the distribution of the more abundant oxides and some trace elements, including the critical metals Nb and REEs. The texture of the pebbles is typical for Apulian karst bauxites and consists of sub-spheroidal ooids composed of boehmite and dispersed in a fine-grained matrix. The growth of the ooids, which formed under dry climate, was described in terms of fractal geometry. The average fractal dimension value of the ooids in the pebbles is close to that of the diffusion-limited aggregation models suggesting the ooid growth can be modelled using a molecular diffusion pattern, based on Fick's first law. The calculated time required for growth of the boehmite concretions is ~ 45 ÷ 310 ka. This finding is consistent with an intra-Campanian emersion event (74–76 Ma) that occurred during a dry and warm climatic stage. Since most of the karst bauxites worldwide have an ooidic texture, evaluation of the composition of concretions and the time required for their growth represents a powerful tool in reconstructing the palaeoenvironment. The zircon grains collected from the pebbles of the Salento-type karst bauxite define several concordant age populations. The youngest cluster, Early Cretaceous in age (99 ÷ 127.5 Ma), suggests that windborne particles from Cretaceous volcanics, possibly originating in the Carpatho-Balkan orogenic belts, provided material for further bauxitisation. The largest cluster (623 ÷ 689 Ma) is of Neoproterozoic age, predominately from the Late Ediacaran and Cryogenian p.p.. The 900–540 Ma Pan-African orogenic cycle was followed by continental-scale uplift and erosion, leading to the deposition of thick Cambrian–Ordovician siliciclastic sequences that represent the most widespread detrital sequence ever deposited on continental crust and that now cover large parts of North Africa. These Cambrian–Ordovician sandstones contain a large population of Neoproterozoic zircons of Cryogenian age. Neoproterozoic zircons also occur in the youngest (Silurian–Mesozoic) sandstones of the Saharan Metacraton. These sandstones also contain 1.0 Ga detrital zircons, suggesting as the oldest zircons found in the Salento-type bauxite pebbles (866 Ma and 941 Ma in age) are younger representatives of the zircon cluster present in this sandstone unit.These zircon age determinations suggest that the source material for the Salento-type bauxite pebbles was a combination of magmatic material from a distant source and clastic material derived from a continental margin (North Africa). This result concurs with the Eu/Eu* vs. Sm/Nd binary diagram, on which bauxite pebbles fall close to a mixing curve with andesite and cratonic sandstone end-members. As our results indicate that material was sourced from the North African continental margin, we suggest that a continental bridge separated oceanic domains in the Late Cretaceous of the Peri-Tethyan domain.     

辽东连山关地区重熔混合岩岩石地球化学特征

连山关地区重熔混合岩位于太古宙钾长花岗岩和浪子山组一段石英岩之间,受韧性剪切带控制,局部地段缺失,为动态部分熔融作用形成。其主量元素以富Si、略富Al、富Na、富K和低Mg、低ca为特点;微量元素表现出富集Be、Mo、Pb、Y、Ba、La、Cu和亏损Co、Ni、Zn、Cr、Ti、V,且与铀关系密切的共生元素有Pb、Mo、V、Be等特点;稀土元素具有明显的轻稀土富集和重稀土相对亏损等特征,具有较显著的Eu负异常。重熔混合岩的成因为韧性剪切作用中围岩的易熔组分不完全、不均匀重熔作用后冷凝再同化形成,重熔混合岩与铀矿化关系密切。     

Concentrations and solubility of heavy metals in muck sediments from the St. Lucie Estuary,U.S.A.

To evaluate muck sediments as a potential soil amendment, total and Mehlich III-extractable concentrations of Cd, Cu, Cr, Ni, Pb, Zn, and Co in 59 muck sediment samples from the St. Lucie Estuary were analyzed. A seven-step chemical fractionation procedure was used to assess the potential mobility of heavy metals. Except for Cd, the average total concentrations of the metals are lower than the reported average concentrations of these elements in municipal composts in the U.S.A. The concentrations were also below critical levels for the safe use of wastes and byproducts in agriculture, as established by the United States Environmental Protection Agency. The Cd, Cu, Cr, Ni, Pb, Zn and Co in the sediments were predominantly associated with silicate minerals in the residual form. Most metals in the muck sediments occur predominantly in weakly mobile or nonbioavailable forms. Use of mucks in neutral pH upland soils should not pose any significant hazards or risk to the environment. However, Cd, Cu, Cr, Ni, Pb, Zn, and Co, especially Zn, Cu, and Pb, could be more readily released from the muck sediments under acidic soil conditions.     

Geochemistry of metals in sediments from the mainstem of the Yellow River, China

Sediment samples at 10 locations in the mainstem of the Yellow River were taken in 1994. Five forms (exchangeable, carbonate, organic, Fe/Mn oxide and residual) of metals were extracted by the Tessier method. The total contents and contents of the five forms of 16 metal elements (Li, Na, K, Ca, Sr, Ba, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, and Al) were determined by ICP-AES. In sediments of the Yellow River, except for Na, mobile elements (such as K, Ca) do not show a negative correlation with the immobile elements. Alkaline metals (Li, Na, and K), Ti, and Al exist mainly in the residual form. The exchangeable forms of alkaline-earth elements (Ca, Sr, and Ba) are the highest, and their residual forms go up with the increase of the period in the periodic table of elements. Half of Mn exists in the residual form, and its non-residual forms exist mainly in carbonate and oxide forms. Except Mn, the iron group elements (Fe, Co, Ni, V, Cr) mainly exist in the residual and oxide forms. High carbonate content of Ca does not cause high contents of other elements in carbonate form, showing that chemical weathering is not strong in the area.     

Mineralogical and geochemical evolution of the Bidgol bauxite deposit,Zagros Mountain Belt,Iran: Implications for ore genesis,rare earth elements fractionation and parental affinity

The present study focuses on the Late Cretaceous Bidgol bauxite deposit in the Zagros Simply Fold Belt, SW Iran. The orebody is located in the eroded major NW–SE trending Koh-e-Hosseyn anticline and hosted as discontinuous stratified layers and lenses within the upper member of the Cenomanian–Turonian Sarvak Formation. Detailed mineralogical analysis reveals that diaspore, hematite, goethite, anatase, clinochlore, chamosite, and calcite are the major mineral components accompanied by minor amounts of detrital and REE-bearing minerals such as rutile, zircon and parisite. The ore texture suggest that the bauxite material has an authigenic origin but in some parts it has been transported short distances from a primary in situ environment and redeposited in karstic depressions. The spheroidal pisolites of the Bidgol bauxite formed under conditions of low water activity, favouring the formation of large diaspore cores and a single dry-to-wet climatic fluctuation. The mass change calculations relative to the immobile element Ti show that elements such as Si, Fe, Mg, K, Na and Sr are leached out of the weathered system; Al, Ni, Zr, Ga, Cr and Ba are concentrated in the residual system; and Hf, Ta, Co, Rb, Cs, Be, and U are relatively immobile during the bauxitisation processes. The Nb, Th, Y, V, Sc, Sn and ΣREE are relatively immobile in the initial stage of bauxitisation processes in the bauxite ores, but were slightly mobile at the later stage of bauxitisation. Geochemical data reveal progressive enrichment of the REE and intense LREE/HREE fractionation toward the lower parts of the bauxite profile. Cerium behaves differently from the other REEs (especially LREE) and show positive anomalies in the upper horizons that gradually become negative in the deeper parts of the profile. The distribution and fractionation of trace elements and REEs during the bauxitisation process in the Bidgol deposit are mainly controlled by the presence of REE-bearing minerals, fluctuations in soil solution pH, REE ionization potential and the presence of bicarbonates or organic matter. Geochemical analyses confirm a protolith contribution from the bedrock argillaceous limestone and suggest that the source material for the Bidgol bauxite was provided from a siliciclastic material derived from a continental margin. The mid-Turonian uplift led to the formation of karstic topography, rubbly breccia and a layer of ferruginous–argillaceous debris that was affected by lateritic weathering under humid tropical climate. Subsequently, mobile elements are removed from the profiles, while Al, Fe and Ti are enriched, resulting in the formation of the pristine bauxite materials. When the platform subsided into the water again, the pristine bauxitic materials were partly converted to bauxite. During the exposure of bauxite orebodies on the limbs and crests of anticlines and subsequent eroding and accumulation in the karstic depressions during folding and faulting in Oligocene–Miocene, important factors such as intensity of the weathering, drainage and floating flow may have improved the qualities of the bauxite ores.     

Geochemical variations of major and trace elements in recent sediments,off the Gulf of Mannar,the southeast coast of India

The Gulf of Mannar along the Tuticorin coast is a coral base of the southeast coast of India. To obtain a preliminary view of its environmental conditions, geochemical distribution of major elements (Si, Al, Fe, Ca, Mg, Na, K, P), trace elements (Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd) and acid leachable elements (Fe, Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd) were analyzed in surface sediment samples from two seasons. Geochemical fractionation confirmed the lithogenic origin of metals, which were mainly associated with the detrital phase. The sediments in the gulf are sandy with abundant calcareous debris, which controls the distribution of total and acid leachable elements. Enrichment factors relative to crust vary by a magnitude of two to three and the presence of trace metals indicates the input of Cr, Pb, Cd, Cu and Zn in both forms through industrial activities. Factor analysis supports the above observation with higher loadings on acid leachable elements and its association with CaCO₃. The increase in concentration of trace metals (Cr, Pb, Cd, Cu, Co, Ni, Zn) along the Gulf of Mannar indicates that the area has been contaminated by the input from riverine sources and the industries nearby. The present study indicates that other sources should be evaluated in the long-term monitoring program.     

岩溶区矿山污染地下水的水生植物修复初步研究

选取黑藻(Hydrilla verticillata Royle)和水绵(Spirogyra communis,Hassall)作为研究对象,分析其对某铅锌矿尾矿库重金属废水的富集能力,综述重金属在黑藻和水绵体内的富集机制,探讨了利用黑藻和水绵进行岩溶矿山重金属污染水修复的应用前景。结果表明:黑藻和水绵体内的重金属绝对含量较高,并且植株长势良好,生物量大,说明这两种水生植物对重金属有避性或耐性。分析测试发现,在黑藻和水绵体内,重金属的富集系数较高,其中Pb最大,其后依次是As>Co>Mn>Cu>Cd>Zn>Ni>Cr,富集系数最少的是Hg,水绵体内的富集系数要大于黑藻。对比研究发现,这两类藻类体内的重金属含量和富集系数均高于非岩溶区。黑藻对重金属的富集机制主要有3种,即重金属作用下抗氧化酶活性增强、被动吸收和离子交换作用,而水绵特殊的分子生物结构可能是其吸附重金属的重要机制。黑藻和水绵在南方岩溶区广泛分布,利用黑藻和水绵修复重金属污染的岩溶水具有较好前景。      

Geochemistry of magnesian ilmenites from kimberlites in South Africa and Lesotho

Magnesium ilmenite from discrete nodules and lamellar intergrowths with pyroxene from the Kao, Sekameng, Frank Smith, and Monastery kimberlites has been analysed for Ti, Fe, Mg, Nb, Zr, Cr, Cu, Zn, Mn, Co, and Ni. Each kimberlite contains discrete ilmenites which exhibit a wide compositional range within the ilmenite-geikeilite series. Lamellar ilmenites from Frank Smith and Monastery differ in composition but both show a limited range in composition which lies within the compositional range shown by discrete ilmenites from these pipes. The ilmenites are enriched in Nb, Zr, Cr, Co, and Ni and depleted in Mn, Cu, and Zn relative to Mg-poor ilmenites from basic intrusions. Nb, Zr, and Ni correlate with Fe, Ti and Mg variations but the abundances of the other trace elements are independent of major element variation. R-mode factor analysis is interpreted to imply that the geochemistry cannot be interpreted in terms of a differentiation hypothesis in which trace elements are removed from or concentrated in residua. Factor scores and major element abundances indicate that each pipe is characterized by a particular suite of discrete ilmenite nodules, which are considered to be phenocrysts in a proto-kimberlite magma. Lamellar ilmenite-pyroxene intergrowths are unlikely to have had a eutectic origin, and show no simple relationship to the discrete ilmenites.     

冲绳海槽南部表层沉积物地球化学特征及其物源和环境指示意义

对冲绳海槽南部陆架、陆坡和海槽 33个表层沉积物进行了元素地球化学分析,结果表明研究区沉积物的主要化学组成为SiO₂ 、Al₂ O₃ 和CaO,这三种组分占沉积物总量的 6 8%左右。多数元素在陆架和陆坡的变化范围较大,在海槽区相对稳定。向海槽方向随沉积物粒径变细,SiO₂ 和CaO减少、Al₂ O₃ 和其它多数元素含量增加。常量元素和Al₂ O₃ 的比值分布特征表明,本区沉积物由物源区经由陆架向海槽输送,沉积物主要由陆源碎屑沉积组成,此外还有生物碎屑沉积和自生沉积。陆架区部分微量元素富集因子 (EF)与长江和黄河沉积物的富集因子对比结果表明,本区的沉积物与长江沉积物的关系更为密切。陆坡区Cu、Pb、Zn、Co、Ni和Cr的富集因子较高是由于生物的富集作用造成的,Mn的富集主要是自生沉积的结果。用R型因子分析方法对沉积物的化学组成进行了分析,结合元素的分布特征,给出了四个主因子所对应的沉积环境和特征元素组合,分别为 1)陆架型的元素组合 :SiO₂ 、TiO₂ 、Zr、CaO和Sr,2 )陆坡型的元素组合Fe₂ O₃ 、MgO和P₂ O₅,3)海槽型的元素组合 :Al₂ O₃ 、K₂ O、Cu、Zn、Co、Ni、Cr和Ba,4 )反映沉积环境氧化-还原属性的元素组合 :MnO和FeO。     

川西同德和沙坝麻粒岩及其退变质岩石之间的元素迁移

利用川西麻粒岩的全岩化学组成与岩石中特征矿物的化学性质,研究了麻粒岩退变质作用的元素迁移。对紫苏辉石、普通辉石和普通角闪石的电子探针分析表明,随着麻粒岩退变质作用程度的加深,矿物的化学组成与全岩的元素迁移同步变化。由于矿物组合和岩相的转变以及地壳流体的作用,同德二辉麻粒岩在退变质至黑云角闪斜长片麻岩过程中,K,Rb,Cs,K／Na,Fe^3+和Fe3+／Fe^2+增加,Fe^2+,V,Co,Ba,Sr和Pb降低;在沙坝二辉麻粒岩退变质为含绿帘石角闪斜长片麻岩过程中,Na,Ca,Fe^3+,Zr,Hf,Nb,Ta,Rb,U,Th,REE和Fe^3+／Fe^2+增加,Fe^2+,Mg,K,Co,Zn,Cs,Pb和K／Na降低。麻粒岩退变质过程中制约不同元素迁移的主要矿物相是普通角闪石等退变质新生矿物。同德和沙坝两个麻粒岩块退变质作用中,个别元素迁移性状并不相同,这可能与原岩的性质和变质流体的成分等环境地质条件有关。     

内蒙古中心屯地区晚侏罗世火山岩岩石地球化学特征及其成因意义

中心屯地区位于大兴安岭火山岩带中南段,区内岩浆活动强烈,发育有中生代不同时期的基性-酸性火山岩。在野外地质调查的基础上,通过研究晚侏罗世火山岩岩石学特征及岩石化学数据,发现区内晚侏罗世火山岩主要为中性-酸性岩石,属于钙碱性系列;稀土元素大都具有铕负异常,配分曲右倾,显示轻稀土元素富集、重稀土元素亏损的特点;微量元素的过渡元素Cr、Co、Ni含量较低,富集大离子亲石元素Rb、Ba、K等,亏损大离子亲石元素Sr,亏损Nb、Th、Ti、P等高场强元素。综合分析表明,晚侏罗世火山岩岩浆来源于地壳。其形成环境处于亚洲大陆边缘断陷带,受太平洋板块俯冲作用的影响。     

Statistical analysis of stream sediment data from the Ife-Ilesha area of Southwest Nigeria

Statistical treatment of geochemical exploration data in the Ife-Ilesha area has not been fully utilized as a tool in their interpretation. The results of 176 stream sediment samples from an area of 1800 km² analyzed for Cu, Zn, Mn, Ni, Co and Cr after hot extraction were treated with both simple and sophisticated (R-mode factor) statistical analytical methods. All the elements were found to have density distributions closely approaching lognormal or a mixture of two lognormal populations.They all show strong positive correlations with correlation coefficient values ranging from 0.5 between Mn and Ni to 0.84 between Mn and Co, all considered to be real at 5% level of significance.R-mode factor analysis produced a three-factor model which accounts for 82.0% of the total variance in the data. Factor 1 (Cu-Co-Ni) correlates spatially with the area underlain by the amphibolite complex, thus reflecting the parent rock as dominant influencing factor. Factor 2 (Mn-Co) and the strong positive correlation between Mn and Co are interpreted as resulting from the influence of Co-adsorption by Mn-oxides. Factor 3 (Zn) is probably a mineralization factor.