Nature and origins of granitic regolith in bauxite mine floors in the Darling Range,Western Australia

Chemical and physical weathering of primary minerals during the formation of laterite profiles in the Darling Range has formed distinct secondary mineral and morphological zones in the regolith. Erosion and human activity such as mining have exposed large areas of lateritic regolith, and its classification is important for land management, especially for mine rehabilitation. Preserved rock fabrics within regolith may enable the identification of parent rock type and degree of weathering, thus providing explanations for variations in important physical properties such as the strength and water retention of regolith. Feldspar, quartz, biotite and muscovite in porphyritic and fine-grained monzogranite in lateritic profiles have weathered via a series of gradational changes to form saprolite and pedolith consisting of kaolin, quartz, iron oxides, muscovite and gibbsite. Local reorganisation in the upper regolith or pedoplasmation zone has included illuviation of kaolin, which may be iron oxide-stained and which has disrupted the preserved rock fabric of saprock and saprolite. Quartz grain- or matrix-supported fabrics have developed, with greater pedoplasmation resulting in a quartz-grain-supported fabric. The recognition of these processes enables the use of gibbsite grainsize and distribution in regolith to infer original feldspar grainsize. Muscovite-rich or muscovite-deficient kaolin matrix indicates where plagioclase or alkali feldspar, respectively, was present in the parent rock. In some regolith, cementing by iron oxides has faithfully preserved rock fabric. The recognition of these various regolith types provides a basis for identifying the parent materials of lateritic regolith developed from granitic and doleritic rocks. Rock fabric is sometimes preserved in iron oxide-cemented bauxite mine floor regolith (Zh) due to the pseudomorphic gibbsite grains and iron oxide cement which forms a porous, rigid fabric. Plagioclase-rich granitoid is more likely to have weathered to dense clay-rich regolith (Zp), whereas albite and alkali feldspar have weathered to quartz-rich regolith (Zm) with the random orientation of quartz grains indicating that substantial reorganisation of rock fabric has occurred. It is possible to predict the response of regolith materials exposed in mine floors to management practices including ripping and re-vegetation, thus allowing targeted use of deep-ripping and planting density based on regolith type.     

Geochemical and mineralogical characteristics of ion-adsorption type REE mineralization in Phuket, Thailand

Geochemical and mineralogical studies were conducted on the 12-m-thick weathering profile of the Kata Beach granite in Phuket, Thailand, in order to reveal the transport and adsorption of rare earth elements (REE) related to the ion-adsorption type mineralization. The parent rock is ilmenite-series biotite granite with transitional characteristics from I type to S type, abundant in REE (592 ppm). REE are contained dominantly in fluorocarbonate as well as in allanite, titanite, apatite, and zircon. The chondrite-normalized REE pattern of the parent granite indicates enrichment of LREE relative to HREE and no significant Ce anomaly. The upper part of the weathering profile from the surface to 4.5 m depth is mostly characterized by positive Ce anomaly, showing lower REE contents ranging from 174 to 548 ppm and lower percentages of adsorbed REE from 34% to 68% compared with the parent granite. In contrast, the lower part of the profile from 4.5 to 12 m depth is characterized by negative Ce anomaly, showing higher REE contents ranging from 578 to 1,084 ppm and higher percentages from 53% to 85%. The negative Ce anomaly and enrichment of REE in the lower part of the profile suggest that acidic soil water in an oxidizing condition in the upper part mostly immobilized Ce⁴⁺ as CeO₂ and transported REE³⁺ downward to the lower part of the profile. The transported REE³⁺ were adsorbed onto weathering products or distributed to secondary minerals such as rhabdophane. The immobilization of REE results from the increase of pH due to the contact with higher pH groundwater. Since the majority of REE in the weathered granite are present in the ion-adsorption fraction with negative Ce anomaly, the percentages of adsorbed REE are positively correlated with the whole-rock negative Ce anomaly. The result of this study suggests that the ion-adsorption type REE mineralization is identified by the occurrence of easily soluble REE fluorocarbonate and whole-rock negative Ce anomaly of weathered granite. Although fractionation of REE in weathered granite is controlled by the occurrence of REE-bearing minerals and adsorption by weathering products, the ion-adsorption fraction tends to be enriched in LREE relative to weathered granite.     

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.     

沉积型铝土矿的陆表淋滤成矿作用: 兼论铝土矿床的成因分类*

铝土矿是化学风化作用的细粒终极产物,与强烈的化学风化作用密切相关。根据母岩的类别及作用过程,风化作用进一步分为铝硅酸盐岩强化学风化形成的红土化作用和碳酸盐岩强化学风化形成的钙红土化作用。在强烈的化学风化过程中,地表的原始沉积物(母岩)的原生矿物发生溶蚀、水解、水化、碳酸化、氧化,破坏原始的矿物结构,形成新的细粒矿物(主要是黏土质矿物)。在适合的地质条件下,持续的强烈化学风化作用会造成大部分活动的元素(如K、Na、Ca、Mg、Si)的流失与Al的残留富集从而形成铝土矿。现在观察到的沉积型铝土矿,虽然与古风化壳具有密切联系,但沉积型铝土矿多数是由沉积过程搬运到沉积盆地中所形成的强化学风化产物的沉积层,与古风化壳的残坡积层具有显著差别,只有少数工业价值不大(品位低、品质差)的残坡积相铝土矿。铝土矿含矿岩系的沉积环境与铝土矿(尤其是高品位、高品质的铝土矿)的成矿环境不尽相同。铝土矿主要形成于暴露于大气中的陆表环境(而非水下环境),由地下水淋滤作用形成(在渗流带由活动元素流失、Al等稳定元素残留富集而成)。本研究在铝土矿成矿作用分析等基础上,提出了以铝土矿沉积物等物源和沉积、成矿作用为依据的中国铝土矿床分类方案,包括原地或准原地残坡积物成因的红土型和喀斯特型,和异地物源沉积成因的沉积型。     

Subaerial leaching process of sedimentary bauxite and the discussion on classifications of bauxite deposits

Bauxite is the ultimate fine-grained products of chemical weathering,and thus it is closely linked with the intense chemical weathering. Based on variations of parent rock and weathering processes,the weathering products can be subdivided into laterite and terra rossa,of which the former is formed by weathering of aluminosilicates and the latter is produced by the weathering of carbonates. During the intense chemical weathering,minerals in original subaerial sediments(parent rocks)would suffer a series of processes(dissolution,hydrolyzation,hydration,carbonation,and oxidation)and be destroyed or transformed,leading to formation of new minerals. In the favorable environment,continuously intense chemical weathering would cause the loss of most mobile elements(e.g., K,Na,Ca,Mg,Si)and the enrichment of Al,resulting in the formation of bauxite. Although sedimentary bauxites are closely linked with the weathering curst,they show obvious differences in formation processes. Sedimentary bauxites are composed of intense chemical weathering products that are transported from outside of the basin and re-deposited in the basin,while most weathering crusts are transformed from saprolite and/or deluvium in-situ,and they can only form low-grade bauxites. Sedimentary environments also differ in bauxite ore layers and bauxitic claystone layers. Bauxite ore layers are formed in the subaerial environment and controlled by the leaching process of groundwater in the vadose zone. Based on the analysis of bauxitization,this study proposes to use multiple parameters,such as provenance,sedimentation and mineralization,to build the new classification of Chinese bauxite deposits. In this classification,lateritic and karstic types of bauxite deposits are autochthonous or parautochthonous saprolite and/or deluvium,while sedimentary type is dominated by heterochthonous provenance.     

Strength and structure of laterites and lateritic soils

Ten soils from Puerto Rico representing various states of weathering were subjected to engineering index tests, strength and density measurement, mineralogic analyses, and scanning electron microscopy.Engineering classification systems used for temperate soils tend to underestimate the engineering behavior of these undisturbed lateritic soils and in the undisturbed state the soils exhibit low densities and high strengths.The engineering properties of the undisturbed soils show systematic trends in relation to the degree of weathering and the parent rock. For a given rock, the void ratio is decreased and cohesion increased as weathering proceeds. This is the result of increasing crystallization and cementation by the sesquioxides.The specific gravity of the solid particles is a promising index property to characterize these lateritic soils insofar as it reflects iron oxide content. The decrease in void ratio and increase in cohesion with increasing specific gravity suggests a model for the engineering classification of tropical soils.     

广东惠东地区离子吸附型稀土矿床地球化学特征

摘要：运用岩石地球化学方法,对广东惠东地区离子吸附型稀土矿床的地球化学特征进行研究。结果显示,风化壳中元素含量及配分特点总体上取决于母岩,但稀土元素在继承母岩稀土元素的基础上含量进一步富集,且各风化层中元素含量变化与风化作用之间具有一定相关性。WIG指数相较于CIA指数能更有效地描述风化壳风化强度,风化壳中稀土元素迁出富集与WIG指数及元素迁移系数具有一定规律性,轻稀土元素多在全风化层上部富集,而重稀土元素在全风化层下部及半风化层明显迁入富集,Ce、Eu均具明显负异常。     

REE Mineralization of Weathered Crust and Clay Sediment on Granitic Rocks in the Sanyo Belt,SW Japan and the Southern Jiangxi Province,China

Rare earth element (REE) geochemistry and mineralogy have been studied in the weathered crusts derived from the Early Yanshanian (Jurassic) biotite granites of Dabu and Dingnan, as well as in the Indosinian (Permian) muscovite–biotite granite of Aigao in southern Jiangxi province, China, and the weathered crusts and clay sediments on biotite granites in the Sanyo belt, SW Japan, that is, Okayama, Tanakami, and Naegi areas. In all of the weathered crusts, biotite and plagioclase commonly tend to decrease toward the upper part of the profile, whereas kaolinite and residual quartz and K‐feldspar increase. The weathered crusts of the Dingnan granites and some Naegi granites, which are characterized by the enrichment in light REE (LREE) in C horizons, have higher total REE (ΣREE) content than the parent REE‐enriched granites. Weathering of LREE‐bearing apatite and fluorocarbonates in the Dingnan granites and allanite and apatite in some Naegi granites may account for the leaching of LREE at the B horizons. The leached LREE must result in subsequent enrichment of LREE in the C horizons. The enrichment is probably associated with mainly adsorption onto kaolinite and partly formation of possible secondary LREE‐bearing minerals. In Japan it was found that REE mineralization occurs not in the weathered granitic crusts but in reworked clay sediments, especially kaolinite‐rich layers, derived mainly from the weathering materials of REE‐enriched granitic rocks. The clay sediments are more enriched in LREE, which likely adsorbed onto kaolinite. Concentration of heavy REE within almost all the weathered crusts and clay sediments, however, may reflect mainly residual REE‐bearing minerals such as zircon, which originated in the parent granitic rocks. The findings of the present study support the three processes for fractionation of the REE during weathering: (i) selective leaching of rocks containing both stable and unstable REE‐bearing minerals; (ii) adsorption onto clay minerals; and (iii) presence of possible secondary LREE‐bearing minerals.     

Behavior of Sm and Nd in a lateritic soil profile

A study of lateritic soils and samples of ground and river waters was carried out in the Nsimi-Zoetele, a tropical watershed in the southern Cameroon. The Nd isotopic compositions and concentrations of Nd and Sm were determined. It was found that the Nd isotopic composition of the river waters was much more radiogenic than the parent rocks, and that the Nd in the waters is not homogeneous but is carried by different dissolved and complexed components that are not isotopically homogenized. The soil profile shows a regular increase in ε_Nd going from the parent rock (ε_Nd = −36) to ε_Nd = −18 near the top of the profile. The Nd transported in the river is thus not representative of the parent rock but reflects the results of differential weathering of constituent minerals and the redeposition of REE in phosphates and a significant contribution of radiogenic Nd from dust. The concentration of Nd in the river water is far above that found in temperate climate rivers and thus this type of tropical river may play a dominant role in the marine Nd and REE budget. It is suggested that the correlation of REE with DOC is related to DOC fixing some dissolved REE but that the REE in solution is governed by other mechanisms. No major shifts were found in Sm/Nd; however, a regular progression from the parent rock through the lateritic profile was found. The upper laterite profile shows large, almost uniform depletions in all REE below Tb and enrichment above. Complementary behavior was found in the lower part of the section. The concentration of Nd relative to the immobile elements Zr and Ti in the laterite is depleted by a factor of ∼10. Th, Nd and Sm are enriched in the lowest zone sampled and must reflect redeposition of REE from the upper part of the weathering section and is associated with phosphate formation. It is concluded that the soil evolution involves both differential dissolution of primary phases from the parent rock, significant to major input of REE from atmospheric dust from other regions, and the formation of diagenetic phases, particularly phosphates.     

Composition and origin of the clay cover on North Brazilian laterites

The Belterra Clay in Northern Brazil is a uniform, yellowish, unstratified kaolinitic clay with variable contents of gibbsite. It is generally 5–10 m thick and covers a lateritic weathering crust on remnants of a dissected table-land. Complete profiles with Belterra Clay, the underlying bauxite/laterite and saprolite/bed rock were sampled in three areas of the Amazon region. The chemical and mineralogical data show a distinct affinity between the Belterra Clay and the underlying layers above all with the saprolite. Variations in the composition of the underlaying layers are reflected by the Belterra Clay. Among the structural and textural features important for the discussion of the origin of the Belterra Clay are the sharp contact between the clay cover and the underlying laterite as well as conglomeritic/brecciate textures and occasional bedding structure in the upper part of the lateritic crust. The detailed analyses do not permit definite conclusions on the origin of the Belterra Clay. Three hypotheses ar discussed:

1. In-situ formation of the clay cover by weathering processes.
2. Clay deposition after lateral transport of saprolitic material coming from former elevations inside or outside the present laterite areas.
3. Vertical transport of the saprolitic material to the surface by termites. However, thicknesses up to 20 m of the Belterra Clay cannot be explained solely by this process.

The compositional relations of the Belterra Clay with the underlying layers are of practical relevance for geological mapping and for mineral exploration.     

特殊地质地貌区填图物化探技术应用

基于物化探技术方法在特殊地质地貌区填图中的应用实验,介绍从区域物化探数据提取地质填图信息的方法,指出重磁与氡-汞气测联合应用是覆盖区探测隐伏岩体、断裂的高效低成本物化探技术组合。运用基于地球化学理论方法的元素地球化学判别技术,在强烈风化区定量划分风化等级为:基岩-弱风化-中度风化-强风化-全风化-残积土等;指出风化壳元素地球化学行为对原生矿物分解、次生矿物形成具有示踪效应;不同风化层稀土元素富集分异显著,强烈富集于全风化层（岩土界面或风化岩石顶界）中的稀土元素分布模式,可作为界定风化壳分层的重要地球化学判别指标。      

Dynamic models of lateritic bauxite formation

2D dynamic models of bauxite formation in the weathering mantle covering denudation areas drained by river systems are discussed. The role of relief-forming factors (tectonic uplift, river erosion and denudation of drainage divides), the interrelation of hydrogeological and lithologic structure of the bauxitebearing weathering mantle, and the dynamics of zoning formation above and below groundwater level are described in the models. Creative and destructive epochs of lateritic bauxite formation differing in tectonic regime are distinguished. During the creative epochs, lateritic weathering develops against a background of decreasing denudation and an increase in areas of bauxite formation. The destructive epochs are characterized by intense denudation, cutting down the areas of lateritic bauxite formation and eventually leading to the complete removal of the weathering mantle. Different morphogenetic types and varieties of bauxite-bearing weathering mantles develop during creative and destructive epochs. The morphology of the weathering mantle sections at the deposits of Cenozoic lateritic bauxite in the present-day tropical zone of the Earth corresponds to the destructive epoch, which is characterized by declining areas of lateritic bauxite formation and will end with complete denudation of lateritic bauxite.     

广西某地花岗岩风化壳中稀土元素特征与iREE矿床成矿机制

为了解风化壳中离子交换相稀土元素的特征,对广西某地花岗岩风化壳剖面样品进行了X射线衍射及主量、稀土元素地球化学特征的研究.剖面自上而下可划分为腐殖土层(A₁)、亚粘土层(A₂)、网纹状风化层(B₁)和全风化层(B₂);自A₁至B₂,粘土矿物的含量和化学风化蚀变指数快速降低;与母岩相比A₁、A₂、B₁中全相Ce、Nd和HREE相对富集,B₂中全相稀土与母岩特征相似,所有样品的离子交换相HREE亏损,Y相对富集;离子交换相轻、重稀土一起富集在B₂中.据此推测,花岗岩中褐帘石、榍石等易风化的稀土矿物为离子交换相稀土提供了主要的物源,锆石、磷钇矿等难风化的稀土矿物的残留及表生稀土矿物的形成使全相HREE相对富集;离子交换相轻、重稀土元素的分馏程度随风化程度的增加而变化.      

Behaviour of REE and mass balance calculations in a lateritic profile over chlorite schists in South Cameroon

An in situ weathering profile overlying chlorite schists in the Mbalmayo-Bengbis formations (South Cameroon) was chosen for the study of the behaviour of REE and the evaluation of geochemical mass balance. After physical and mineralogical studies, the chlorite schists and the undisturbed weathered materials were chemically analyzed for major elements (X-ray fluorescence and titrimetry) and REE (ICP-MS). The behaviour of the REE in the Mbalmayo weathering system was established in comparison with the REE of the reference parent rock. Mass balance calculations were applied to both major elements and REE. The mineralogy of the materials was determined with the aid of a Philips 1720, diffractometer. The chlorite schists of the Mbalmayo sector show low REE contents (Σ=153.44 ppm). These rocks are relatively rich in LREE (about 125 times the chondritic value) and relatively poor in HREE (about 20 times the chondritic value). The REE diagram normalized to chondrites shows a slightly split graph ((La/Yb)_N=6.18) with marked enrichment in LREE (LREE/HREE=9.50) in relation to HREE. Moreover, these spectra do not present any Ce anomaly, but a slightly positive Eu anomaly. The imperfectly evolved profile, whose materials are genetically linked, shows an atypical behaviour of REE. In effect, the LREE are more mobile than the HREE during weathering ((La/Yb)NASC<1) with weak Ce anomalies. This has been rarely reported in lateritic profiles characterized by higher HREE mobility than LREE during weathering processes with high Ce anomalies. This is either due to the difference in the stability of REE-bearing minerals, or to the weak acidic to basic pH conditions (6.70<pH<7.80), or even due to the average evolution of the weathering materials. The pathway of the REE along the profile is as follows: (1) leaching in the saprolites and summit of the profile, except for Ce, which precipitates very weakly in the nodular materials and the coarse saprolite materials, (2) at the base of the profile, solutions come in contact with chlorite schist formations, at this level, the pH increases (pH=7.79), HREE and a part of LREE partially void of Ce precipitate and (3) the other part of LREE precipitates further up in the profile. The geochemical mass balance calculations reveal that these elements are leached in the same phases as the relatively high Si, Al, K and Fe²⁺ contents.     

The Los Pijiguaos bauxite deposit (Venezuela): A compilation of field data and implications for the bauxitization process

Chemical, mineralogical, and petrographic data from the Los Pijiguaos bauxite deposit, together with the water chemistry of the streams draining the area, were used to study the problem of lateritic bauxite formation at this location. The Los Pijiguaos bauxite, located at the northwestern edge of the Guayana Shield in Venezuela, is a lateritic bauxite developed on a Precambrian Rapakivi Granite Batholith, the Parguaza Granite. This deposit is situated on a planation surface at elevations between 600 and 700 m; it is believed to have originated during an erosional event that took place during Late Cretaceous-early Tertiary times.The weathering profile is composed of an upper bauxite zone, followed by a saprolite, and merging gradually to the fresh granite. The upper bauxitic zone contains gibbsite, quartz, hematite, and goethite. The saprolite contains kaolinite, quartz, and goethite and is characterized by a relict granitic texture that indicates little bulk volume change associated with the weathering process. The upper bauxitic zone has lost any textural resemblance with the parent granite, consistent with extensive volume loss.Bauxite and saprolite are separated by a transition zone where gibbsite and kaolinite coexist. Textures indicating the replacement of kaolinite by gibbsite point to the dynamic nature of the weathering profile, characterized by advancing reaction fronts.The chemical composition of the deposit defines trends that can be traced back to the composition of the parent granite and shows enrichment of Al₂O₃, Fe₂O₃, and TiO₂, and depletion of SiO₂, relative to the parent granite. The uppermost part of the profile is characterized by a further enrichment of Fe₂O₃ with respect to the other components of the bauxite. Important volume and mass losses in the bauxite have also been calculated, based on chemical composition and density measurements. The calculated losses are consistent with the textural observations in the bauxite.The chemical composition of the waters of streams draining the area shows strong seasonal patterns, consistent with the seasonal nature of the local climate (one dry and one rainy season per year, both about six months long). The balance between dissolved and suspended loads in these streams indicates that the magnitudes of chemical and physical denudation are similar, leading to approximately constant thicknesses of the weathering profiles. These observations are consistent with model calculations based on current climatic conditions and suggest that the bauxitization process is still active.     

加纳阿瓦索红土型铝土矿床地球化学特征及成矿作用研究

红土型铝土矿是加纳共和国铝土矿资源的主要矿床类型。阿瓦索铝土矿床产于西非克拉通古元古界比理姆岩系(泥板岩类)的表层红土中,是典型的红土型铝土矿。通过分析阿瓦索铝土矿的成矿地质背景、矿体特征以及矿石地球化学元素特征发现,铝土矿石的化学组分以Al_2O_3、SiO_2、TFe_2O_3为主,TiO_2次之,碱金属元素含量极低;风化过程中Zr、Hf、Nb、Ta等微量元素含量稳定;Cr—Ni关系图显示比理姆岩系为铝土矿的矿源岩,三水铝石主要由比理姆岩系中的黏土矿物经过风化淋滤形成,表层铝土矿在后期风化和红土化作用下结构构造发生一定的变化,铁氧化成以赤铁矿为主的铁壳,最终形成一个大型的红土型铝土矿。     

The supergene thorium and rare-earth element deposit at Morro do Ferro, Poços de Caldas, Minas Gerais, Brazil

The thorium and rare-earth element (Th-REE) deposit at Morro do Ferro formed under supergene lateritic weathering conditions. The ore body consists of shallow NW-SE elongated argillaceous lenses that extend from the top of the hill downwards along its south-eastern slope. The deposit is capped by a network of magnetite layers which protected the underlying highly weathered, argillaceous host rock from excessive erosion. The surrounding country rocks comprise a sequence of subvolcanic phonolite intrusions that have been strongly altered by hydrothermal and supergene processes.From petrological, mineralogical and geochemical studies, and mass balance calculations, it is inferred that the highly weathered host rock was originally carbonatitic in composition, initially enriched in Th and REEs compared to the surrounding silicate rocks. The intrusion of the carbonatite caused fenitic alteration in the surrounding phonolites, consisting of early potassic alteration followed by a vein-type Th-REE mineralization with associated fluorite, carbonate, pyrite and zircon. Subsequent weathering has completely decomposed the carbonatite forming a residual supergene enrichment of Th and REEs.Initial weathering of the carbonatite has created a chemical environment that might have been conductive to carbonate and phosphate complexing of the REEs in groundwaters. This may have appreciably restricted the dissolution of primary REE phases. Strongly oxidic weathering has resulted in a fractionation between Ce and the other light rare earth elements (LREEs). Ce³⁺ is oxidized to Ce⁴⁺ and retained together with Th by secondary mineral formation (cerianite, thorianite), and by adsorption on poorly crystalline iron- and aluminium-hydroxides. In contrast, the trivalent LREEs are retained to a lesser degree and are thus more available for secondary mineral formation (Nd-lanthanite) and adsorption at greater depths down the weathering column. Seasonally controlled fluctuations of recharge waters into the weathering column may help to explain the observed repetition of Th-Ce enriched zones underlain by trivalent LREE enriched zones.     

河南省荥巩煤田大峪沟矿段深部铝土矿床地质特征及找矿方向

荥巩煤田大峪沟矿段深部铝土矿床是最近找矿突破发现的一个大型铝土矿床。该铝土矿床成矿时代为早二叠世,成矿物源主要为古陆铝硅酸岩风化物,少量为中奥陶统马家沟组碳酸盐岩风化产物,成矿环境为潮坪-沼泽环境,由长期的沉积间断、特定的岩相古地理环境、构造变形和表生风化作用共同控制着矿床的形成;上石炭统本溪组是铝土矿形成的含矿岩系;海湾泻湖相沉积环境是铝土矿床形成的有利条件;下古生界奥陶系、寒武系古岩溶侵蚀面是铝土矿形成的有利场所,古岩溶侵蚀面洼地及漏斗是铝土矿的定位空间。大峪沟矿段铝土矿床成因模式属于"古陆风化+碎屑和化学沉积";成矿机制为机械和化学分异。含矿岩系底部铁质风化壳/铁质黏土岩为碳酸盐岩风化形成,铝(黏)土矿来源于铝硅酸盐岩。大峪沟深部铝土矿床的发现为河南省寻找深部铝土矿床指明了方向。     

Negative cerium anomalies in the saprolite zone of serpentinite lateritic profiles in the Lomié ultramafic complex,South-East Cameroon

Strong negative cerium anomalies are developed in the saprolite zone of two serpentinite lateritic profiles in the Mada region of the Kongo–Nkamouma massif in the Lomié ultramafic complex (South-East Cameroon).The total lanthanide contents increase strongly from the parent rock (1.328 ppm) to the weathered materials (ranging from 74.32 to 742.18 ppm); the highest value is observed in the black nodules from the western weathering profile and the lowest one in the top of the clayey surface soil from the same profile. The lanthanide contents, except cerium, are highest in the saprolite and decrease along the profile. The light REE contents are very high compared to those of the heavy REE (LREE/HREE ranging from 3.21 to 44.37). The lanthanides normalized with respect to the parent rock reveal: (i) strong negative Ce anomalies with [Ce/Ce¹] ranging from 0.006 to 0.680 in the saprolite zone; (ii) strong positive Ce anomalies with [Ce/Ce¹] ranging from 1.23 to 23.96 from the top of the saprolite to the clayey surface horizon; (iii) positive Eu anomalies with [Eu/Eu¹] ranging from 2.09 to 2.41 in all the weathered materials.Mass balance evaluation shows that, except cerium, lanthanides have been highly accumulated in the saprolite zone and moderately concentrated in the upper part of both profiles. Cerium has been highly accumulated in the nodules of the West Mada profile. The presence of negative Ce anomalies is confirmed by its low degree of accumulation whereas the positive ones are related to its high degree of accumulation.     

河南伊川石佛寺铝土矿地质特征及控矿因素

河南伊川石佛寺铝土矿是近年在豫西地区龙门-巩义铝土矿成矿带新发现的中型铝土矿床之一.矿床含矿岩系为上石炭统本溪组中下部,铝土矿呈层状产于寒武系崮山组碳酸盐岩古风化剥蚀面,与上覆太原组整合接触.矿床赋存的本溪组从下而上分别由含铁黏土岩和铝土矿层组成.铝土矿体直接顶板为一1煤,厚约0.80～1.60 m;直接底板为高铁铝质...