Arsenic in contaminated soils and anthropogenic deposits at the Mokrsko,Roudný, and Kašperské Hory gold deposits,Bohemian Massif (CZ)

Soil, mine tailing, and waste dump profiles above three mesothermal gold deposits in the Bohemian Massif with different anthropogenic histories have been studied. Their mineralogical, major element, and arsenic (As) contents and the contents of secondary arsenic minerals were analyzed. The As-bearing minerals were concentrated and determined using X-ray diffraction (XRD) analysis, the Debye-Scherrer powder method, scanning electron microscopy (SEM), and energy-dispersive microanalysis (EDAX). The amorphous hydrous ferric oxides (HFO), As-bearing goethite, K-Ba- or Ca-Fe- and Fe- arsenates pharmacosiderite, arseniosiderite, and scorodite, and sulfate-arsenate pitticite were determined as products of arsenopyrite or arsenian pyrite oxidation. The As behaviour in the profiles studied differs in dependence on the surface morphology, chemical and mineralogical composition of the soil, mine wastes or tailings, oxidation conditions, pH, presence of (or distance from) primary As mineralization in the bedrock, and duration of the weathering effect. Although the primary As mineralization and the bedrock chemical composition are roughly similar, there are distinct differences in the As behaviour amongst the Mokrsko, Roudný and Kaperské Hory deposits.     

山西大同钾镁煌斑岩地质地球化学特征

根据饮牛沟钾镁煌斑岩的岩石学、岩石化学、矿物化学、微量及稀土元素地球化学特征,本文认为该岩体属钾镁煌斑岩,但在矿物成分及化学成分上与世界上典型的含金刚石的钾镁煌斑岩相比,相对贫钛和钾,未出现含Ｋ,Ｂａ,Ｔｉ,Ｚｒ的副矿物。该岩体的成因可能为母岩部分熔融后又经分离结晶作用而形成的,岩浆起源于贫钛的金云母二辉橄榄岩,形成深度１００ｋｍ左右。     

Modelling weathering processes at the catchment scale: The WITCH numerical model

A numerical model of chemical weathering in soil horizons and underlying bedrock (WITCH) has been coupled to a numerical model of water and carbon cycles in forest ecosystems (ASPECTS) to simulate the concentration of major species within the soil horizons and the stream of the Strengbach granitic watershed, located in the Vosges Mountains (France). For the first time, simulations of solute concentrations in soil layers and in the catchment river have been performed on a seasonal basis. The model is able to reproduce the concentrations of most major species within the soil horizons, as well as catching the first-order seasonal fluctuations of aqueous calcium, magnesium and silica concentrations. However, the WITCH model underestimates concentrations of Mg²⁺ and silica at the spring of the catchment stream, and significantly underestimates Ca²⁺ concentration. The deficit in calculated calcium can be compensated for by dissolution of trace apatite disseminated in the bedrock. However, the resulting increased Ca²⁺ release yields important smectite precipitation in the deepest model layer (in contact with the bedrock) and subsequent removal of large amount of silica and magnesium from solution. In contrast, the model accurately accounts for the concentrations of major species (Ca, Mg and silica) measured in the catchment stream when precipitation of clay minerals is not allowed. The model underestimation of Mg²⁺ and H₄SiO₄ concentrations when precipitation of well crystallized smectites is allowed strongly suggests that precipitation of well crystallized clay minerals is overestimated and that more soluble poorly crystallized and amorphous materials may be forming. In agreement with observations on other watersheds draining granitic rocks, this study indicates that highly soluble trace calcic phases control the aqueous calcium budget in the Strengbach watershed.     

Hydrothermal mobility of Ti, Zr and REE: examples from the Bergell and Adamello contact aureoles (Italy)

Contact metamorphic marbles, affected by metasomatic fluids at the contact to the Bergell and Adamello Intrusives, contain various accessory minerals (zirconolite, allanite, titanite, rutile, geikielite, hoegbomite), which provide new evidence for the hydrothermal mobility of Ti and Zr. In both examples, Ti and Zr migrated along with U, Th, Y and REE in a metasomatic fluid rich in potassium. The composition of the main minerals (fluorine-rich phlogopite, pargasite and titanian clinohumite) and the abundance of fluor-apatite demonstrate that fluorine and phosphorus were important components of the fluid. The textural relationships indicate that the formation of the accessory phases is linked to the crystallization of the hydrous minerals.     

Geological controls on soil parent material geochemistry along a northern Manitoba–North Dakota transect

As a pilot study for mapping the geochemistry of North American soils, samples were collected along two continental transects extending east–west from Virginia to California, and north–south from northern Manitoba to the US–Mexican border and subjected to geochemical and mineralogical analyses. For the northern Manitoba–North Dakota segment of the north–south transect, X-ray diffraction analysis and bivariate relations indicate that geochemical properties of soil parent materials may be interpreted in terms of minerals derived from Shield and clastic sedimentary bedrock, and carbonate sedimentary bedrock terranes. The elements Cu, Zn, Ni, Cr and Ti occur primarily in silicate minerals decomposed by aqua regia, likely phyllosilicates, that preferentially concentrate in clay-sized fractions; Cr and Ti also occur in minerals decomposed only by stronger acid. Physical glacial processes affecting the distribution and concentration of carbonate minerals are significant controls on the variation of trace metal background concentrations.     

The effect of organic matter on chemical weathering: study of a small tropical watershed: nsimi-zoétélé site,cameroon

The effect of organic matter during soil/water interaction is still a debated issue on the controls of chemical weathering in a tropical environment. In order to study this effect in detail, we focused on the weathering processes occurring in a small tropical watershed (Nsimi-Zoetélé, South Cameroon). This site offers an unique opportunity to study weathering mechanisms in a lateritic system within a small basin by coupling soil and water chemistry.The lateritic cover in this site can reach up to 40 m in depth and show two pedological distinct zones: unsaturated slope soils on the hills and/or elevated areas; and water-saturated soils in the swamp zone which represent 20% of the basin surface. The study present chemical analysis performed on water samples collected monthly from different localities between 1994–1997 and on soil samples taken during a well drilling in December 1997. The results suggest the existence of chemical and spatial heterogeneities of waters in the basin: colored waters flooding the swamp zone have much higher concentrations of both organic matter (i.e., DOC) and inorganic ions (e.g., Ca, Mg, Al, Fe, Th, Zr) than those from springs and groundwater from the hills. Nevertheless, these organic-rich waters present cation concentrations (Na, Ca, Mg, K) which are among the lowest compared to that of most world rivers. The main minerals in the soils are secondary kaolinite, iron oxi-hydroxides, quartz, and accessory minerals (e.g., zircon, rutile). We mainly focused on the mineralogical and geochemical study of the swamp zone soils and showed through SEM observations the textural characterization of weathered minerals such as kaolinite, zircon, rutile, and the secondary recrystallization of kaolinite microcrystals within the soil profile. Water chemistry and mineralogical observations suggest that hydromorphic soils of the swamp zone are responsible for almost all chemical weathering in the basin. Thus, in order to explain the increase of element concentration in the organic-rich waters, we suggest that organic acids enhance dissolution of minerals such as kaolinite, goethite, and zircon and also favors the transport of insoluble elements such as Al, Fe, Ti, Zr, and REE by chemical complexation. SiO₂(aq) concentrations in these waters are above saturation with respect to quartz. Dissolution of phytholithes (amorphous silica) may be responsible for this relatively high SiO₂(aq.) concentration. Al/Mg ratios obtained for the soil and the Mengong river waters show that a significant amount of Al does not leave the system due to kaolinite recrystallisation in the swamp zone soils. Geochemical data obtained for this watershed show the important contribution of vegetation and organic matter on chemical weathering in the swamp zone. Quantitatively we propose that the increasing amount in total dissolved solid (TDS) due to organic matter and vegetation effect is about 35%. In summary, this interaction between soils and waters occurs mostly in soils that are very depleted in soluble elements. Thus, the low concentration of major elements in these water is a direct consequence of the depleted nature of the soils.     

Mineralogy,major and trace element geochemistry of riverbed sediments in the headwaters of the Yangtze,Tongtian River and Jinsha River

We collected riverbed sediments of the headwaters of the Yangtze River (Chumaer River, Tuotuo River, Gaerqu River and Buqu River), Tongtian River and Jinsha River (HTJR) flowing on the eastern Tibetan Plateau and analyzed their mineralogical features, major and trace element contents. The results show: (i) very poor correlations of Na₂O, K₂O, CaO, Ba, and Sr to SiO₂, LREE to Th, HREE to Hf, and Ta/La to Ti, and characteristics of Eu anomaly (the ratios of (Eu/Eu^*)_N range from 0.60 to 0.83 with an average value of 0.71) all indicate that the Jinsha River sediments have not undergone much mineralogical sorting; (ii) illite and chlorite are predominant clay minerals, and quartz, calcite, dolomite, albite, and K-feldspar are prevailing non-clay minerals. The characteristics of mineral assemblage indicate relatively weak chemical weathering degree in these river basins; (iii) very high contents of Fe₂O₃, MgO, TiO₂, Sc, V, Cr, Co, and Ni at Panzhihua mainly result from the huge-sized V–Ti magnetite deposits occurred in layered gabbroic intrusion; and (iv) the chemical alteration index (CIA) in the HTJR ranges from 46.5 to 69.2 and with an average value of 60.5 which indicates relatively weak weathering degree.     

Constraints from high-pressure veins in eclogites on the composition of hydrous fluids in subduction zones

Hydrous high-pressure veins formed during dehydration of eclogites in two paleo-subduction zones (Trescolmen locality in the Adula nappe, central Alps and Münchberg Gneiss Massif, Variscan fold belt, Germany) constrain the major and trace element composition of solutes in fluids liberated during dehydration of eclogites. Similar initial isotopic compositions of veins and host eclogites at the time of metamorphism indicate that the fluids were derived predominantly from the host rocks. Quartz, kyanite, paragonite, phengite, zoisite and omphacite are the dominant minerals in the veins. The major element compositions of the veins are in agreement with experimental evidence indicating that the composition of solutes in such fluids is dominated by SiO₂ and Al₂O₃. Relative to N-MORB, the veins show enrichments of Cs, Rb, Ba, Pb, and K, comparable or slightly lower abundances of Sr, U, and Th, and very low abundances of Nd, Sm, Zr, Nb, Ti and Y. The differential fractionation of highly incompatible elements such as K, U and Th in the veins, as well as the presence of hydrous minerals in the eclogites rule out partial melting as a cause for vein formation. These results confirm previous suggestions that fluids derived from subducted basalt may have low abundances of high field strength elements, rare earth elements and Y. Variable vein-eclogite enrichment factors of incompatible alkalis and to a lesser extent Pb appear to reflect mineralogical controls (phengite, epidote-group minerals) on partitioning of these elements during dehydration of eclogite in subduction zones. However, abundance variations of incompatible elements in minerals from eclogites suggest that the composition of fluids released from eclogites at temperatures <700°C may not reflect true equilibrium partitioning during dehydration. Simple models for the trace elements U and Th indicate the relative importance of the basaltic and sedimentary portions of subducted oceanic crust in producing the characteristic chemical signatures of these elements in convergent plate margin volcanism.     

Petrographic-geochemical types of Triassic alkaline ultramafic rocks in the Northern Anabar province,Yakutia, Russia

A classification suggested for alkaline ultramafic rocks of the Ary-Mastakh and Staraya Rechka fields, Northern Anabar Shield, is based on the modal mineralogical composition of the rocks and the chemical compositions of their rock-forming and accessory minerals. Within the framework of this classification, the rocks are indentified as orangeite and alkaline ultramafic lamprophyres: aillikite and damtjernite. To estimate how much contamination with the host rocks has modified their composition when the diatremes were formed, the pyroclastic rocks were studied that abound in xenogenic material (which is rich in SiO₂, Al₂O₃, K₂O, Rb, Pb, and occasionally also Ba) at relatively low (La/Yb)_PM, (La/Sm)_PM, and not as much also (Sm/Zr)_PM and (La/Nb)_PM ratios. The isotopic composition of the rocks suggests that the very first melt portions were of asthenospheric nature. The distribution of trace elements and REE indicates that one of the leading factors that controlled the diversity of the mineralogical composition of the rocks and the broad variations in their isotopic–geochemical and geochemical characteristics was asthenosphere–lithosphere interaction when the melts of the alkaline ultramafic rocks were derived. The melting processes involved metasomatic vein-hosted assemblages of carbonate and potassic hydrous composition (of the MARID type). The alkaline ultramafic rocks whose geochemistry reflects the contributions of enriched vein assemblages to the lithospheric source material, occur in the northern Anabar Shield closer to the boundary between the Khapchan and Daldyn terranes. The evolution of the aillikite melts during their ascent through the lithospheric mantle could give rise to damtjernite generation and was associated with the separation of a C–H–O fluid phase. Our data allowed us to distinguish the evolutionary episodes of the magma-generating zone during the origin of the Triassic alkaline ultramafic rocks in the northern Anabar Shield.     

Mineralogical and geochemical investigations of the Mombi bauxite deposit,Zagros Mountains,Iran

The Mombi bauxite deposit is located in 165 km northwest of Dehdasht city, southwestern Iran. The deposit is situated in the Zagros Simply Fold Belt and developed as discontinuous stratified layers in Upper Cretaceous carbonates (Sarvak Formation). Outcrops of the bauxitic horizons occur in NW-SE trending Bangestan anticline and are situated between the marine neritic limestones of the Ilam and Sarvak Formations. From the bottom to top, the deposit is generally consisting of brown, gray, pink, pisolitic, red, and yellow bauxite horizons. Boehmite, diaspore, kaolinite, and hematite are the major mineral components, while gibbsite, goethite, anatase, rutile, pyrite, chlorite, quartz, as well as feldspar occur to a lesser extent. The Eh–pH conditions during bauxitization in the Mombi bauxite deposit show oxidizing to reducing conditions during the Upper Cretaceous. This feature seems to be general and had a significant effect on the mineral composition of Cretaceous bauxite deposits in the Zagros fold belt. Geochemical data show that Al₂O₃, SiO₂, Fe₂O₃ and TiO₂ are the main components in the bauxite ores at Mombi and immobile elements like Al, Ti, Nb, Zr, Hf, Cr, Ta, Y, and Th were enriched while Rb, Ba, K, Sr, and P were depleted during the bauxitization process. Chondrite-normalized REE pattern in the bauxite ores indicate REE enrichment (ΣREE = 162.8–755.28 ppm, ave. ∼399.36 ppm) relative to argillic limestone (ΣREE = 76.26–84.03 ppm, ave. ∼80.145 ppm) and Sarvak Formation (ΣREE = 40.15 ppm). The REE patterns also reflect enrichment in LREE relative to HREE. Both positive and negative Ce anomalies (0.48–2.0) are observed in the Mombi bauxite horizons. These anomalies are related to the change of oxidation state of Ce (from Ce³⁺ to Ce⁴⁺), ionic potential, and complexation of Ce⁴⁺ with carbonate compounds in the studied horizons. It seems that the variations in the chemistry of ore-forming solutions (e.g., Eh and pH), function of carbonate host rock as a geochemical barrier, and leaching degree of lanthanide-bearing minerals are the most important controlling factors in the distribution and concentration of REEs. Several lines of evidences such as Zr/Hf and Nb/Ta ratios as well as similarity in REE patterns indicate that the underlying marly limestone (Sarvak Formation) could be considered as the source of bauxite horizons. Based on mineralogical and geochemical data, it could be inferred that the Mombi deposit has been formed in a karstic environment during karstification and weathering of the Sarvak limy Formation.     

桂西平果教美矿区堆积型铝土矿形成过程中矿物转化与元素迁移

桂西地区铝土矿为典型喀斯特型,包括二叠系沉积型和第四系堆积型两亚类。堆积型铝土矿是沉积型铝土矿经抬升、破碎、风化,最后堆积于喀斯特洼地中形成。以平果教美铝土矿为研究对象,探索堆积型铝土矿形成过程中矿物的变化与元素迁移。沉积型矿石的矿物组成包括硬水铝石、鲕绿泥石、锐钛矿及少量针铁矿、金红石和高岭石;堆积型矿石的矿物组成主要为硬水铝石、锐钛矿、高岭石及少量三水铝石和鲕绿泥石。转化过程中堆积型矿石中的硬水铝石含量明显增加,鲕绿泥石含量明显减少。沉积型铝土矿的主要化学组成为Al₂O₃、SiO₂、FeO和TiO₂;堆积型为Al₂O₃、SiO₂、TiO₂和Fe₂O₃。两类矿石中元素Zr 、Ba、Nb、V含量均较高,稀土总量变化大,富集轻稀土。质量平衡计算表明堆积型铝土矿形成过程中Al、Ba、Sr、Y等元素增加,而Si、Fe、Ti、Nb、V、Ce等元素减少,其余元素变化不明显。     

广西红黏土矿物成分分析

黏土矿物成分对其工程力学性质具有显著的影响。目前,在黏土矿物种类鉴定方面已有一些成熟的方法技术,而对黏土的矿物成分定量分析尚没有成熟的方法。本文基于X射线衍射试验、全化学元素分析、Bogue法和K值法,对广西武鸣、桂林两地红黏土的矿物成分进行了定性鉴定和定量分析。研究结果表明:(1)桂林、武鸣两地红黏土的主要矿物均为高岭石、三水铝石、针铁矿,桂林红黏土还含有一定量的石英。(2)武鸣红黏土的矿物成分及其含量依次为:高岭石(74.0%)、三水铝石(12.53%)、针铁矿(2mm, 2.22%)、针铁矿(2mm, 8.37%)。(3)桂林红黏土的矿物成分及其含量依次为:高岭石(56.59%)、三水铝石(11.44%)、针铁矿(15.61%)、石英(12.45%)。     

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.     

Origin of felsic volcanism in the Izu arc intra-arc rift

An intra-arc rift (IAR) is developed behind the volcanic front in the Izu arc, Japan. Bimodal volcanism, represented by basalt and rhyolite lavas and hydrothermal activity, is active in the IAR. The constituent minerals in the rhyolite lavas are mainly plagioclase and quartz, whereas mafic minerals are rare and are mainly orthopyroxene without any hydrous minerals such as amphibole and biotite. Both the phenocryst and groundmass minerals have felsic affinities with a narrow compositional range. The petrological and bulk chemical characteristics are similar to those of melts from some partial melting experiments that also yield dry rhyolite melts. The hydrous mineral-free narrow mineral compositions and low-Al₂O₃ affinities of the IAR rhyolites are produced from basaltic middle crust under anhydrous low-temperature melting conditions. The IAR basalt lavas display prominent across-arc variation, with depleted elemental compositions in the volcanic front side and enriched compositions in the rear-arc side. The across-arc variation reflects gradual change in the slab-derived components, as demonstrated by decreasing Ba/Zr and Th/Zr values to the rear-arc side. Rhyolite lavas exhibit different across-arc variations in either the fluid-mobile elements or the immobile elements, such as Nb/Zr, La/Yb, and chondrite-normalized rare earth element patterns, reflecting that the felsic magmas had different source. The preexisting arc crust formed during an earlier stage of arc evolution, most probably during the Oligocene prior to spreading of the Shikoku back-arc basin. The lack of systematic across-arc variation in the IAR rhyolites and their dry/shallow crustal melting origin combines to suggest re-melting of preexisting Oligocene middle crust by heat from the young basaltic magmatism.     

Sequential extraction of labile elements and chemical characterization of a basaltic soil from Mt. Meru,Tanzania

We conducted a modified Bureau Commun Reference (BCR) sequential extraction on a basaltic soil (phono-tephrite) from Mt. Meru in Northern Tanzania in order to determine the relative contribution of water soluble, carbonate and exchangeable, oxide and organic fractions to the bulk composition of the soil. Elemental compositions were determined by ICP-MS and corrected for loss on ignition. Relatively immobile elements, such as Zr, Hf and Al, are enriched by 10–30% compared to the unweathered protolith, consistent with soil formation being accompanied by mass loss due to chemical weathering. However, superimposed on this mass loss appears to be enrichment of elements such as Fe, Ca and Mg, especially towards the surface. In some cases, the bulk concentrations of these elements at the surface exceed that of the protolith. These data suggest that the surface of the Meru soil columns may have experienced “re-fertilization” by the deposition of volcanic ash. From the carbonate and exchangeable extraction, we found evidence of clay rich horizons which may sequester as much as 5% of the bulk K. The concentration of calcium carbonate appears to decrease with depth, but the largest incorporation of Sr and Ba into carbonates occurs below 114 cm. Fe and Mn oxides scavenge more than 10–20% of total Ti, V, Co, Cu, Zr and Pb below 114 cm. The organic fraction sequestered significant fractions of total Al, Cu, REE’s and Pb throughout the soil column.     

A geochemical and mineralogical investigation of some British and other European tonsteins

The volcanic origin of a number of major tonstein horizons has been established from mineralogical compositions and from trace elements that are quantitatively retained during diagenesis. Discriminant function analysis using the variables Ti/Al, Cr/Al, Zr/Al and Ni/Al allows the tonsteins to be classified according to original composition. Two main groups are recognized amongst the British tonsteins. Those formed from acid volcanic ash are comparable in composition with French and German tonsteins and a common source is postulated, whereas tonsteins formed from basic volcanic ash contain variable amounts of detrital sediment and are thought to originate from local eruptions. Possible lateral equivalents between tonstein horizons in Britain and elsewhere in Europe are suggested.     

Evidence of Mid-ocean ridge and shallow subduction forearc magmatism in the Nagaland-Manipur ophiolites,northeast India: constraints from mineralogy and geochemistry of gabbros and associated mafic dykes

We discuss here the mineralogical and geochemical characteristics of mafic intrusive rocks from the Nagaland-Manipur Ophiolites (NMO) of Indo-Myanmar Orogenic Belt, northeast India to define their mantle source and tectonic environment. Mafic intrusive sequence in the NMO is characterized by hornblende-free (type-I) and hornblende-bearing (type-II) rocks. The type-I is further categorized as mafic dykes (type-Ia) of tholeiitic N-MORB composition, having TiO₂ (0.72–1.93 wt.%) and flat REE patterns (La_N/Yb_N = 0.76–1.51) and as massive gabbros (type-Ib) that show alkaline E-MORB affinity, having moderate to high Ti content (TiO₂ = 1.18 to 1.45 wt.%) with strong LREE-HREE fractionations (La_N/Yb_N = 4.54–7.47). Such geochemical enrichment from N-MORB to E-MORB composition indicates mixing of melts derived from a depleted mantle and a fertile mantle/plume source at the spreading center. On the other hand, type-II mafic intrusives are hornblende bearing gabbros of SSZ-type tholeiitic composition with low Ti content (TiO₂ = 0.54 wt.%–0.86 wt.%) and depleted LREE pattern with respect to HREE (La_N/Yb_N = 0.37–0.49). They also have high Ba/Zr (1.13–2.82), Ba/Nb (45.56–151.66) and Ba/Th (84.58–744.19) and U/Th ratios (0.37–0.67) relative to the primitive mantle, which strongly represents the melt composition generated by partial melting of depleted lithospheric mantle wedge contaminated by hydrous fluids derived from subducting oceanic lithosphere in a forearc setting. Their subduction related origin is also supported by presence of calcium-rich plagioclase (An_16.6–32.3). Geothermometry calculation shows that the hornblende bearing (type-II) mafic rocks crystallized at temperature in range of 565°–625 °C ± 50 (at 10 kbar). Based on these available mineralogical and geochemical evidences, we conclude that mid ocean ridge (MOR) type mafic intrusive rocks from the NMO represent the section of older oceanic crust which was generated during the divergent process of the Indian plate from the Australian plate during Cretaceous period. Conversely, the hornblende-bearing gabbros (type-II) represent the younger oceanic crust which was formed at the forearc region by partial melting of the depleted mantle wedge slightly modified by the hydrous fluids released from the subducting oceanic slab during the initial stage of subduction of Indian plate beneath the Myanmar plate.     

发育完整的灰岩风化壳及其矿物学和地球化学特征

对于碳酸盐岩土覆土壤成因、尽管碳酸盐岩风化残积成土说被多数学者认同,但由于碳酸盐岩中酸不溶物含量极低,在风化成土过程中会伴随着巨大的体积缩小变化,原岩结构和半风化带无法保留,从而缺失了探索上覆土壤物质来源的重要中间环节,使得这种观点缺乏野外宏观证据的支持。最近,我们在贵州、湖南等地发现了数个以泥质灰岩和泥质白云岩为基岩的碳酸盐岩风化壳剖面,尚保留有较好的原岩结构,具有明显的风化壳分带和过渡现象。这些风化壳剖面的发现为深入研究碳酸盐岩风化成土过程提供了良好的研究场所。本文选取了较为典型的吉首泥灰岩风化壳剖面,从矿物学地球化学的角度来探讨碳酸盐岩风化壳的形成过程和发育特征,结果表明该风化壳既遵循非碳酸盐岩（主要是结晶岩类）风化壳的发育特征,也具有自己独特的地球化学演化规律。风化壳总体特点受碳酸盐中的酸不溶物矿物组合及化学成分的影响甚至控制,风化非碳酸盐风壳相似的发育特征。吉首泥灰岩风化壳剖面的发育特征和作者早先提出 的碳酸盐岩风化成土的两阶段模式是一致的,即以碳酸盐矿物大量淋失、酸不溶物逐渐堆积或残积为特征的早期阶段和残积物进一步风化成土的阶段,后一阶段的演化类似非碳酸盐岩类的风化过程。     

The mineralogy and geochemistry of two copper-rich weathering profiles in Burkina Faso, West Africa

Two weathering profiles developed over disseminated Cu mineralization hosted by granodiorites (porphyry type) and felsic volcanics respectively, in a savannah tropical environment (Burkina Faso) have been studied in detail. A mineralogical and geochemical study was carried out in order to determine the characteristics of both profiles and the behaviour of Cu in such deeply weathered environments. Our investigation was focused on the upper part of the weathering profile, respectively 4.0 and 10.5 m below the surface.The mineralogical study reveals that in the first case (profile A) the predominant clay minerals are smectites and kaolinite while in the second (profile B) a more kaolinitic composition is indicative of more severe leaching. In fact, field observations seem to demonstrate that the latter situation is more clearly related to an ancient lateritic-type weathering while the first one results from more recent processes.In both cases the Cu contents through the profiles are high (several thousands of ppm) and in good agreement with the grades obtained in depth, in the mineralized rock. Nevertheless, some leaching can be observed in the upper soil horizons, but the contents still remain highly anomalous, in the 1000 ppm range.It is shown that Cu is distributed in the main secondary minerals constituting the weathering products, whether they are silicates (smectites, phyllites, kaolinites) or oxides (goethite, hematite, Mn oxides).The main stable Cu-bearing mineral seems to be the kaolinite: indeed, smectites turn into kaolinite in the upper part of the profiles while goethite seems to be depleted in Cu under the same conditions.As concerns geochemical exploration, two observations can be noted. Firstly, Cu is very stable in such supergene environments, and secondly, the best size fraction in which to detect the Cu secondary dispersion haloes in soil or stream sediment samples is the <63 μ fraction, in terms of anomaly intensity or contrast.     

Melting of hydrous pyroxenites with alkali amphiboles in the continental mantle: 2. Trace element compositions of melts and minerals

The trace element compositions of melts and minerals from high-pressure experiments on hydrous pyroxenites containing K-richterite are presented. The experiments used mixtures of a third each of the natural minerals clinopyroxene, phlogopite and K-richterite, some with the addition of 5% of an accessory phase ilmenite, rutile or apatite. Although the major element compositions of melts resemble natural lamproites, the trace element contents of most trace elements from the three-mineral mixture are much lower than in lamproites. Apatite is required in the source to provide high abundances of the rare earth elements, and either rutile and/or ilmenite is required to provide the high field strength elements Ti, Nb, Ta, Zr and Hf. Phlogopite controls the high levels of Rb, Cs and Ba.Since abundances of trace elements in the various starting mixtures vary strongly because of the use of natural minerals, we calculated mineral/melt partition coefficients (D_Min/melt) using mineral modes and melting reactions and present trace element patterns for different degrees of partial melting of hydrous pyroxenites. Rb, Cs and Ba are compatible in phlogopite and the partition coefficient ratio phlogopite/K-richterite is high for Ba (1 3 6) and Rb (12). All melts have low contents of most of the first row transition elements, particularly Ni and Cu ((0.1–0.01) × primitive mantle). Nickel has high D_Min/melt for all the major minerals (12 for K-richterite, 9.2 for phlogopite and 5.6 for Cpx) and so behaves at least as compatibly as in melting of peridotites. Fluorine/chlorine ratios in melts are high and D_Min/melt for fluorine decreases in the order apatite (2.2) > phlogopite (1.5) > K-richterite (0.87). The requirement for apatite and at least one Ti-oxide in the source of natural lamproites holds for mica pyroxenites that lack K-richterite. The results are used to model isotopic ageing in hydrous pyroxenite source rocks: phlogopite controls Sr isotopes, so that lamproites with relatively low ⁸⁷Sr/⁸⁶Sr must come from phlogopite-poor source rocks, probably dominated by Cpx and K-richterite. At high pressures (>4 GPa), peritectic Cpx holds back Na, explaining the high K₂O/Na₂O of lamproites.