焦作煤田石炭-二叠纪泥质岩地球化学特征及古环境意义

泥质岩的地球化学特征蕴含了大量地质信息,在物源和沉积环境分析中的应用十分广泛。利用X射线荧光光谱仪和电感耦合等离子体质谱仪（ICP-MS）对华北板块南缘焦作煤田石炭-二叠纪泥质岩样品进行常量元素、微量元素（包括稀土元素）进行分析,并据此讨论泥质岩的物源性质、物源区岩石风化作用强度及当时古环境特征。研究区泥质岩的高Al₂O₃/TiO₂值及低Cr/Zr和K₂O/Al₂O₃值特征,以及泥质岩Zr-TiO₂和Th/Co-La/Sc源岩判别图、Ni-Cr图和（Gd/Yb）_N-Eu/Eu*图等的判别分析结果,都揭示了研究区泥质岩物源主要为后太古宙长英质岩石;Al₂O₃-CaO*+Na₂O-K₂O（A-CN-K）图和较高的黏土矿物成分反映了泥质岩源区受到钾交代作用的影响,致使CIA（化学蚀变指数）值被低估;高CIW（化学风化指数）值和Al₂O₃-CaO*-Na₂O（A-C-N）判别图分析结果表明泥质岩物源区母岩在石炭-二叠纪经历了强烈的风化作用;Sr/Ba和B/Ga比值变化指示本溪组沉积时期到太原组沉积早期为海相为主的沉积环境,太原组沉积中期到山西组沉积早期为海陆过渡相为主的沉积环境,山西组沉积中期到上石盒子组沉积时期为陆相沉积环境。     

Geochemistry and provenance of stream sediments of the Ganga River and its major tributaries in the Himalayan region,India

Major, trace and REE compositions of sediments from the upper Ganga River and its tributaries in the Himalaya have been examined to study the weathering in the Himalayan catchment region and to determine the dominant source rocks to the sediments in the Plains. The Ganga River rises in the Higher Himalaya from the Higher Himalayan Crystalline Series (HHCS) bedrocks and traverses over the Lesser Himalayan Series (LHS) and the Himalayan foreland basin (Siwaliks) rocks before entering into the Gangetic Plains. The major element compositions of sediments, reflected in their low CIA values (45.0–54.7), indicate that silicate weathering has not been an important process in the Himalayan catchment region of the Ganga River. Along the entire traverse, from the HHCS through LHS and the Siwaliks, the sediments from the tributaries and the mainstream Ganga River show higher Na₂O, K₂O, CaO and silica. This, and the higher ratios of La/Sc, Th/Sc and lower ratios of Co/Th, suggest that the source rocks are felsic. The fractionated REE patterns and the significant negative Eu anomalies (Eu/Eu? = 0.27–0.53) indicate highly differentiated source. Moreover, the comparison of the sediments with different source rock lithologies from the HHCS and the LHS for their major elements clearly suggests that the HHCS rocks were the dominant source. Further, comparison of their UCC (upper continental crust) normalized REE patterns suggests that, among the various HHCS rocks, the metasediments (para-gneiss and schist) and Cambro-Ordovician granites have formed the major source rocks. The Bhagirathi and Alaknanda River sediments are dominantly derived from metasediments and those in the Mandakini River from Cambro-Ordovician granites. The resulting composition of the sediments of the Ganga River is due to the mixing of sediments supplied by these tributaries after their confluence at Devprayag. No further change in major, trace and rare earth element compositions of the sediments of the Ganga River after Devprayag up to its exit point to the Plains at Haridwar, suggests little contribution of the Lesser Himalayan and Siwalik rocks to the Ganga River sediments.     

松辽盆地南部哈达山附近青山口组二、三段泥岩的岩石学与地球化学特征

以松辽盆地哈达山青山口组二、三段泥岩盖层为研究对象,通过岩石学和地球化学相结合的方法,对泥岩样品中常量元素和稀土微量元素特征进行了研究,结果表明:(1)泥岩稀土元素(∑REE)总量较高(104.99×10~(-6)~281.88×10~(-6)),∑LREE/HREE比值较高(6.50~9.96),REE配分模式显示轻稀土元素富集而重稀土元素亏损,Eu(0.88~1.16)存在负异常等特征;(2)物源区母岩类型主要为沉积岩和中基性火山岩,源岩的钾交代作用成因可能为黏土矿物中的伊蒙混层转化为自生伊利石;(3)物源区泥岩修正后的CIA值(44.75~72.24)较低,暗示物源区经历了弱风化作用,Sr/Cu指标显示物源区长期受干热型气候控制。     

Geochemistry of phosphate bearing sedimentary rocks in parts of Sonrai block,Lalitpur District,Uttar Pradesh,India

Major, trace and rare earth elements of phosphatic rocks around Sonrai block of Paleo-Mesoproterozoic age having phosphatic breccia, quartzite, shale, sandstone, limestone and ironstone, have been determined to evaluate their correlation, relationship with the phosphorus content, the nature of possible substitution of various elements and regional distribution pattern over the area. The study indicates that the number of elements is substituted in the apatite structures; few of them are associated with phosphate and carbonate minerals. The variable concentration of major, trace and rare earth elements in the phosphatic rocks has been influenced by various physico-chemical processes involved during weathering and leaching of the source rocks. The distribution of the major, trace and rare earth elements is controlled by the environmental variations in the sediment water interface. The majority of trace elements were mainly influenced by the principle adsorbents like the phosphate minerals in addition to clay, iron oxides and silicate minerals. The PAAS normalized REE patterns of Sonrai block of phosphorites are characterized by negative Ce anomalies and Positive Eu anomalies. It is inferred from the distribution and interrelationship of major, trace and rare earth elements that the deposition of phosphate minerals might have occurred in highly oxidizing to slightly reducing conditions in supratidal to intertidal continental margins and shallow marine environment. The deposition was controlled by marine upwelling leading to excess charge of phosphate in certain zones of phosphogenic basins, lithologic facies variations in restricted circulations of basinal waters and electrochemical factors such as negative Eh, pH and other factors, which influenced the deposition of phosphates. The replacement, precipitation in voids and fissures and diagenesis were also important mechanisms of phosphate generation in Sonrai basin. The main source for various elements may be the minerals of cratonic mass of Bundelkhand Granitic Complex, a basement of Bijawar Basin, which also provided land derived phosphorus through weathering of the terrestrial cover.     

右江盆地中三叠世碎屑岩地球化学特征及其物源分析∶以贵州册亨地区为例

右江盆地中三叠世充填了一套巨厚的复理石沉积,岩性为细砂岩、粉砂岩、泥岩及其过渡岩石,其独特的沉积特征颇受国内外地质学界关注,但目前对该套碎屑岩的物源尚有争议。文章通过对册亨地区中三叠世碎屑岩开展详细的岩石学和地球化学分析,结果显示：碎屑岩成分成熟度与结构成熟度都较低,具近源沉积特征。SiO₂（平均为58.49%）含量较低,变化范围较大,说明石英含量较低;Al₂O₃（平均为12.46%）含量较高,说明粘土矿物及长石含量较高;Al₂O₃/SiO₂的比值平均为0.22,与杂砂岩（0.20~0.23）一致,说明碎屑岩成熟度较差,亦具近源沉积特征;CaO（平均为7.83%）含量较高,说明含碳酸盐类物质较多。微量元素表现为富集Rb、Th、La、Nd、Hf和Pb以及相对亏损P、Ti、Sr、Nb和Ta的特点,稀土元素具有ΣREE变化范围大,轻稀土富集,Eu亏损的特点。主量、微量和稀土元素分析表明,碎屑岩的源岩以长英质岩石为主,并有少量中性岩及石英质沉积岩的混入;源区构造背景以大陆岛弧为主,兼有被动大陆边缘及活动大陆边缘特 征。化学蚀变指数（CIA）值为53.93~74.80,均值为65.12。通过CIA以及Th/U比值,表明碎屑岩源区主要经历了中等化学风化作用。     

煤系高岭岩的地球化学判别标志

本文主要研究了煤系高岭岩的微量、稀土、氧同位素地球化学特征。根据高岭岩产出层序、岩石学、矿物学、地球化学特征的研究，将煤系高岭岩分为两类：（１）铝土质高岭岩，微量元素含量、稀土总量，氧同位素值高，稀土配分模式与典型北美页岩相似，Ｅｕ负异常，反映其源岩为风化壳化学风化作用产物。（２）夹矸高岭岩，微量元素含量，稀土总量，氧同位素值低，稀土配分模式部分与典型北美页岩相似，反映其源岩与铝土质高岭岩类似；部     

Trace elements and REE fractionation in subsoils developed on sedimentary and volcanic rocks: case study of the Mt. Vulture area,southern Italy

There is an increasing interest in the distribution of rare earth elements (REEs) within soils, primarily as these elements can be used to identify pedogenetic processes and because soils may be future sources for REE extraction, despite much attention should be paid to the protection and preservation of present soils. Here, we evaluate the processes that control the distribution of REEs in subsoil horizons developed over differing lithologies in an area of low anthropogenic contamination, allowing estimates of the importance of source rocks and weathering. Specifically, this study presents new data on the distribution of REEs and other trace elements, including transition and high-field-strength elements, in subsoils developed on both Quaternary silica-undersaturated volcanic rocks and Pliocene siliciclastic sedimentary rocks within the Mt. Vulture area of the southern Apennines in Italy. The subsoils in the Mt. Vulture area formed during moderate weathering (as classified using the chemical index of alteration) and contain an assemblage of secondary minerals that is dominated by trioctahedral illite with minor vermiculite. The REEs, high-field-strength elements, and transition metals have higher abundances in subsoils that developed from volcanic rocks, and pedogenesis caused the Mt. Vulture subsoils to have REE concentrations that are an order of magnitude higher than typical values for the upper continental crust. This result indicates that the distribution of REEs in soils is a valuable tool for mineral exploration. A statistical analysis of inter-elemental relationships indicates that REEs are concentrated in clay-rich fractions that also contain significant amounts of low-solubility elements such as Zr and Th, regardless of the parent rock. This suggests that low-solubility refractory minerals, such as zircon, play a significant role in controlling the distribution of REEs in soils. The values of (La/Yb)_N and (Gd/Yb)_N fractionation indices are dependent on the intensity of pedogenesis; soils in the study area have values that are higher than typical upper continental crust ratios, suggesting that soils, especially those that formed during interaction with near neutral to acidic organic-rich surface waters, may represent an important source of both light REEs and medium REEs (MREEs). In comparison, MREE/heavy REE fractionation in soils that form during moderate weathering may be affected by variations in parent rock lithologies, primarily as MREE-hosting minerals, such as pyroxenes, may control (La/Sm)_N index values. Eu anomalies are thought to be the most effective provenance index for sediments, although the anomalies within the soils studied here are not related to the alteration of primary minerals, including feldspars, to clay phases. In some cases, Eu/Eu* values may have a weak correlation with elements hosted by heavy minerals, such as Zr; this indicates that the influence of mechanical sorting of clastic particles during sedimentary transport on the Eu/Eu* values of siliciclastic sediments needs to be considered carefully.     

Rare earth distributions in clay minerals and in the clay-sized fraction of the Lower Permian Havensville and Eskridge shales of Kansas and Oklahoma

The REE (rare earth element) content of a wide variety of clay mineral groups have been analyzed using radiochemical neutron activation and have been found to be quite variable in absolute REE content (range of ∑REE = 5.4–1732) and less variable in relative REE content (range of chondritenormalized La/Lu = 0.9–16.5). The variable REE content of the clay mineral groups is probably determined by the REE content of the source rock from which the clay mineral was derived and not from the separate minerals in the rock.The clay-sized fractions of the Havensville and Eskridge shales of Kansas and Oklahoma have similar relative REE distributions and identical negative Eu anomaly size as the composite of NAS (N. American shales), but an absolute REE content (range of ∑REE = 46–348) that may differ significantly from the composite of NAS. The clay-sized fraction of samples from any given outcrop did not vary much in absolute or relative REE content, but samples from northern Oklahoma, probably composed of continental to near-shore marine sediments, have higher absolute REE contents and higher La/Lu ratios than samples of marine deposits in Kansas (e.g. mean ∑REE in Oklahoma = 248; mean ∑REE in Kansas = 69–116). The differencess in the REE content between samples in Oklahoma and Kansas may be caused by chemical weathering processes in the source area, exchange reactions in the environment of deposition, or diagenesis and do not appear to be a result of the different clay minerals.Most samples have Eu anomalies relative to chondrites (range of Eu/Sm ratios of samples = 0.035–1.17; chondrites = 0.35). Some montmorillonites and kaolinites are anomalous in Eu relative to the NAS (range of Eu/Sm ratios of samples = 0.056–0.21; NAS = 0.22). These anomalies may be inherited from source rocks with Eu anomalies originally produced by igneous processes, or they may be produced by chemical weathering processes in the source area.     

Geochemistry and mineralogy of the Al-rich shale from Baluti formation,Iraqi Kurdistan region: implications for weathering and provenance

The mineralogical and geochemical characteristics of the Upper Triassic Baluti shale from the Northern Thrust Zone (Sararu section) and High Folded Zone (Sarki section) Kurdistan Region, Iraq, have been investigated to constrain their paleoweathering, provenance, tectonic setting, and depositional redox conditions. The clay mineral assemblages are dominated by kaolinite, illite, mixed layers illite/smectite at Sararu section, and illite > smectite with traces of kaolinite at Sarki. Illite, to be noted, is within the zone of diagenesis. The non-clay minerals are dominated by calcite with minor amounts of quartz and muscovite in Sararu shale; and are dominated by dolomite with amounts of calcite and quartz in Sarki shale. Baluti shale is classified as Al-rich based on major and minor elements. The chemical index of alteration (CIA) is significantly higher in the Sararu than the Sarki shales, suggesting more intense weathering of the Sararu than the Sarki shales. The index of compositional variability (ICV) of the Sararu shale is less than 1 (suggesting it is compositionally mature and was deposited in a tectonically quiescent setting). More than 1 for Sarki shales (suggest it is less mature and deposited in a tectonically active setting). Most shale of the Baluti plot parallel and along the A-K line in A-CN-K plots suggest intense chemical weathering (high CIA) without any clear-cut evidence of K-metasomatism. Clay mineral data, Al enrichment, CIA values, and A-CN-K plot suggest that the source area experienced high degree of chemical weathering under warm and humid conditions, especially in Sararu. Elemental ratios critical of provenance (La/Sc, Th/Sc, Th/Cr, Th/Co, Ce/Ce*_PN, Eu/Eu*_PN, and Eu/Eu*_CN) shows slight difference between the Sararu and Sarki shales; and the ratios are similar to fine fractions derived from the weathering of mostly felsic rocks. The Eu/Eu^* _CN, Th/Sc, and low K₂O/Al₂O₃ ratios of most shales suggest weathering from mostly a granodiorite source rather than a granite source, consistent with a source from old upper continental crust. Discrimination diagrams based on major and trace element content point to a role of the felsic-intermediate sources for the deposition of Baluti Formation, and probably mixed with mafic source rocks at Sararu section. The chondrite-normalized rare earth elements (REE) patterns are similar to those of PAAS, with light REE enrichment, a negative Eu anomaly, and almost flat heavy REE pattern similar to those of a source rock with felsic components. The source of sediments for the Baluti Formation was likely the Rutba Uplift and/or the plutonic-metamorphic complexes of the Arabian Shield located to the southwest of the basin; whereas the Sararu shale was affected by the mafic rocks of the Bitlis-Avroman-Bisitoun Ridge to the northeast of Arabian Plate. The tectonic discrimination diagrams, as well as critical trace and REE characteristic parameters imply rift and active setting for the depositional basin of the shale of Baluti Formation. The geochemical parameters such as U/Th, V/Cr, V/Sc, and Cu/Zn ratios indicate that these shales were deposited under oxic environment and also show that Sarki shale was deposited under more oxic environment than Sararu.     

赣南小流域水体中稀土元素的地球化学特征

本文以赣南小流域水体为研究对象,利用VG Axiom高分辨多接受双聚焦等离子体质谱仪测定了水体中溶解态稀土元素(DREE)的含量,分析了水体中DREE的分布分异机制,并探讨了稀土元素(REE)产生分异的原因.结果表明,赣南所有的采样区水体中Ce都表现为负异常,说明其在风化壳中少活化.受自然风化作用控制为主的水体相对于页岩除Ce亏损、Eu富集外产生的分异很小,其中Eu的正异常源于Eu富集矿物的优先溶解;蒸发盐矿影响下的水体相对于自然作用为主的水体DREE没有发生明显分异;受稀土矿影响的水体中重稀土元素(HREE)富集、Eu负异常的分布模式继承了稀土矿区风化壳的特征;赣州市下游干流水体中中稀土元素(MREE)富集、Eu负异常的分布模式主要是人为影响的结果.     

中国大陆架海底沉积物中的稀土元素

选择渤海、黄海、东海和南海有代表性的大陆架沉积物样品,利用X射张荧光光谱法测定了15个稀土元素。中国大陆架沉积物稀土元素的丰度为156ppm,相对接近于中国黄土和花岗岩的丰度,而与太平洋沉积物的丰度相差较远,具有明显的“亲陆性”。稀土的配分模式旦显著的负斜率,属陆壳稀土的典型特征。稀土含量受沉积物粒度控制。实验表明稀土主要以类质同像存在于粘土矿物之晶体构造中。根据数理统计,稀土与亲陆源粘土矿物的元素为一类,彼此呈正相关;与亲海洋生物的元素为负相关。事实说明中国大陆岩石的风化和搬运,是中国海大陆架沉积物中稀土的主要物质来源。     

松辽盆地钱家店地区姚家组赋矿砂岩的组成、地球化学特征及其构造背景

松辽盆地钱家店地区姚家组砂岩矿物、地球化学成分与源区岩石性质和沉积构造环境密切相关。岩相学观察和矿物化学分析表明,所研究的岩石主要碎屑矿物由石英、岩屑和长石组成,含少量的黄铁矿、炭屑和重矿物等矿物。地球化学特征上,这些岩石普遍具有高SiO2含量(68.4%~79.61%)、相对高的K2O/Na2O比值(1.83~2.03)和较低的Fe2O3T+MgO含量(1.48%~4.22%),稀土元素标准化配分曲线呈现轻稀土富集,重稀土平坦和弱Eu、Ce负异常特征。较低的CIA(57~63)和PIA(60~71)指数、A-CN-K以及AK-C-N分布模式还说明源区经历了相对较弱的风化作用。Zr/Sc和Th/Sc比值共同表明姚家组的碎屑组成不具备沉积再旋回的特征,说明其为近源沉积,具有较差的分选性。砂岩物源区组成判别图研究表明,姚家组砂岩的物源区主要出露长英质岩浆岩。砂岩形成构造环境判别图解及特征指数分析表明,姚家组主要形成于被动大陆边缘沉积环境。     

Geochemical evolution of the Tertiary succession of the NW shelf,Bengal basin,Bangladesh: Implications for provenance,paleoweathering and Himalayan erosion

Whole rock major, trace and rare earth element (REE) compositions of Paleogene to Neogene sedimentary rocks of the NW shelf succession (Province 1) of Bangladesh contain a record of interaction of the India and Asian plates, Himalayan tectonism, and climatic development. Analyses of 66 sandstones and mudrocks from the Tertiary succession of Bangladesh were made to examine provenance, source weathering, and the influence of paleoclimate and tectonism. The sediments display linear geochemical trends due to quartz dilution, and varying quartz–clay ratios produced by hydrodynamic sorting. Chondrite-normalized REE patterns for both sandstones and mudrocks from different groups are similar to upper continental crust, with moderate to high LREE enrichment (lithotypes within formations average La_N/Yb_N 5.31–11.41) and marked negative Eu anomalies (Eu/Eu^* 0.51–0.69). Based on geochemical criteria the succession can be divided into three parts (Jaintia; Barail–Surma; and Dupi Tila). Very high silica contents in Jaintia Tura sandstones and high Chemical Index of Alteration (CIA) indices in Kopili mudrocks (Fe-shales) suggest derivation from a deeply weathered and stable cratonic source (India). The Tura sandstones are interpreted as first-cycle quartz arenites, produced while the Indian plate drifted across equatorial regions during the Paleocene–Eocene Thermal maximum (PETM). The Barail–Surma and Dupi Tila sediments were derived from a felsic orogen (the Himalaya). The Barail–Surma sediments were mainly derived from the Trans Himalayan Batholith and associated granitoids, with significant contribution from the Lesser Himalaya. Mafic input is also evident, probably from intraoceanic arc material within the Himalaya. Barail mudrocks have uniformly high CIA values (92–95), suggesting intense steady-state weathering of their proto-Himalayan source, and warm and humid climate. In contrast, CIA values of Surma mudrocks range from 66 to 93 (average 84), suggesting non-steady state weathering related to active uplift in the Himalaya. The Dupi Tila sediments were derived from a more felsic Lesser Himalaya source, with significant contribution from the Trans-Himalaya and very little or no ophiolitic or arc material. Dupi Tila mudrocks have CIA ratios of 62–99 (average 72), also indicating non-steady state weathering in the rising Himalayan source. Geochemical compositions of the NW shelf sediments are comparable to coeval successions in the Surma basin (Province 2) of Bangladesh and the Siwaliks (India), indicating similar source. Evolution of the Indian monsoon and associated high precipitation caused intense chemical weathering of the Surma and Dupi Tila source, despite rapid uplift. The Surma Group thus bears the signature of evolution of the Asian monsoon in the Bengal basin at 21 Ma, simultaneous with the development of the East Asian monsoon. This supports proposals that both monsoon systems developed at the same time.     

Geochemistry,provenance and tectonic setting of the Late Cambrian–Early Ordovician Seydişehir Formation in the Çaltepe and Fele areas,SE Turkey

The major, trace and rare earth element (REE) contents of metapelite (MPL), metapsammite (MPS) and metamarl (MM) samples from the Cambro-Ordovician Seydi?ehir Formation were analyzed to investigate their provenance and tectonic setting. The MPS, MPL, and MM samples have variable SiO₂ concentrations, with average values of 72.36, 55.54, and 20.95 wt%, moderate SiO₂/Al₂O₃ ratios (means of 6.88, 3.23, and 3.80), moderate to high Fe₂O₃ + MgO contents (means of 5.14, 9.55, 3.56 wt%), and high K₂O/Na₂O ratios (means of 3.26, 3.64, 2.90), respectively. On average, the chemical index of alteration (CIA) values of the MPS and the MPL are 65.87 and 71.96, respectively, while the chemical index of weathering (CIW) values are 74.54 and 85.09, respectively. These data record an intermediate to high degree of alteration (weathering) of plagioclase to illite/kaolinite in the samples’ provenance. The chondrite-normalized REE patterns of all the sample groups are similar and are characterized by subparallel light rare earth elements (LREE)-enriched, relatively flat heavy rare earth elements (HREE) patterns with pronounced Eu anomalies (mean of 0.69) and moderate fractionation [average (La/Yb)_N = 8.7]. Plots of sediments in ternary diagrams of La, Th, Sc and elemental ratios (La/Sc, Th/Sc, Cr/Th, Eu/Eu*, La/Lu, Co/Th, La/Sc and Sc/Th), which are critical for determining provenance, and REE patterns indicate that the metaclastic units of the Seydi?ehir Formation were derived dominantly from felsic to intermediate magmatic rocks and not from a mafic source. The La–Sc–Th and Th–Sc–Zr/10 ternary diagrams of the Seydi?ehir Formation are typical of continental island arc/active continental margin tectonic settings. The geologic location and geochemistry of the Seydi?ehir Formation suggest that it was deposited in an Andean-type retroarc foreland basin during the Late Cambrian–Early Ordovician period. The Neoproterozoic intermediate to felsic magmatic rocks and metaclastic sediments with felsic origins of the Sand?kl?–Afyon Basement Complex (SBC) and their equivalent units, which are thought to be overlain by the younger units in the study area, may be the dominant source rocks for the Seydi?ehir Formation.     

Geochemistry of Çoruh River Bed Sediments in NE Turkey: Implications in Weathering-Sedimentary Cycle,Provenance, and Metal Pollution

This study defines the source area, sub-aerial weathering, and sedimentary cycle level, as well as heavy metal content and origin, of the Çoruh River bed sediments. The studied sediments are geochemically classified as litharenite based on the ratio of the major element contents. Relative to the Upper Continental Crust (UCC), trace elements Rb, Sr, Ba, Th, U, Zr, Hf, Y, Nb, and Pb are generally depleted; Co, Ni, Cu, Sc, and V are generally enriched; and Au is depleted in some places and enriched in other places. The rare earth element (REE) distributions of the samples exhibit a trend similar to that of the upper continental crust (UCC); however, low to moderate depletion occurs in the bed sediments in UCC. The analyzed samples exhibit low Chemical Index of Alteration (CIA) values, Plagioclase Index of Alteration (PIA) values (<50), CIA/WIP (Weathering Index ratios <1), and substantially high Index of Compositional Variability values (ICV) (>1). Thus, the samples are not chemically mature and are mainly derived from non-altered sources and were exposed the simple cycling history. REEs are depleted in the river bed sediments, unlike the world river average silt, world river average clay, and suspended sediment in world rivers. Minor enrichment of Zn, Sn, and Sc contents, low-to-moderate enrichment of Cu content, very severe enrichment of as content, and extremely severe enrichment of Ni content of the analyzed samples are observed. Consequently, stream bed sediments are derived from intermediate sources close to mid-continental crust rather than felsic sources Low-to-moderate degrees of chemical weathering of these sediments indicate increased tectonic activity, increased erosion, and rapid sedimentation in semiarid to arid conditions in the source regions over time. Thus, the sediments are chemically immature. These sediments are exposed to lithogenic and anthropogenic contamination.     

Provenance and tectonic setting of the metapelites deposits in the Bulfat Complex,NE-Iraq

Major and trace elements including rare earth elements (REEs) chemistry of the metapelitic rocks of Bulfat Complex (Iraqi Zagros Suture Zone) indicate their enrichment in large-ion Lithophile, light rare earth (LREE) elements, and relative depletion of high field strength and heavy rare earth (HREE) elements. The linear correlation coefficients between TiO₂, K₂O, and Al₂O₃ and total REE reveal that phyllosilicates (e.g., mica) and accessory minerals mainly Ti-bearing phases (e.g., ilmenite) are likely the dominant hosts for REEs. Chondrite-normalized REE patterns typical of continental margin settings with significant enrichment of LREE, prominent negative Eu anomalies, and nearly flat HREE are positively correlated with post-Archean Australian shale (PAAS) and upper continental crust (UCC) patterns. Additionally, their consistent elemental La/Sc, Th/Sc, La/Co, Th/Co, Cr/Th, and Eu/Eu* values suggest that sediments may have been originally derived from an old post-Archean upper continental crust composed chiefly of granitic component. It seems most likely that the felsic source rocks were originated by a process of intra-crustal differentiation such as partial melting and/or fractional crystallization involving fractionation of Ca-plagioclase. The geochemical evidences particularly REEs evaluation show that deposition of clasts occurred in an active continental margin setting during lower–upper Cretaceous period contemporaneous with the igneous activities. It is evident therefore that the clasts source is from the north–northeast side, i.e., from the active margin of Iranian microcontinent (Sanandaj–Sirjan Zone).     

Mineralogical and geochemical characteristics of Miocene pelitic sedimentary rocks from the south-western part of the Pannonian Basin System (Croatia): Implications for provenance studies

Fifty-two samples of Miocene pelitic sedimentary rock from outcrops on Medvednica,Moslavacka Gora and Psunj Mts.,and boreholes in the Sava Depression and the Pozega Sub-depression were investigated.These sediments formed in different marine(with normal and reduced salinity),brackish,and freshwater environments,depending on the development stage of the Pannonian Basin System.Carbonate minerals,clay minerals and quartz are the main constituents of all pelitic sedimentary rocks,except in those from Moslavacka Gora Mt in which carbonate minerals are not present.Feldspars,pyrite,opal-CT,and hematite are present as minor constituents in some rocks.Besides calcite,dependent on the sedimentary environment and diagenetic changes,high-magnesium calcite,aragonite,dolomite and ankerite/Cadolomite are also present.Smectite or illite-smectite is the main clay minerals in the samples.Minor constituents,present in almost all samples,are detrital illite and kaolinite.In some samples chlorite is also present in a low amount.Major elements,trace elements and rare earth elements patterns used in provenance analysis show that all analysed samples have a composition similar to the values of the upper continental crust(UCC).The contents of major and trace elements as well as SiO_2/Al_2O_3,K_2O/Al_2O_3,Na_2O/K_2O,Eu/Eu~*,La/Sc,Th/Sc,La/Co Th/Co,Th/Cr,Ce/Ce~* and LREE/HREE ratios,show that the analysed pelitic sedimentary rocks were formed by weathering of different types of mostly acidic(silicic),i.e.felsic rocks.     

皖南姚村岩体花岗岩风化壳稀土元素赋存特征

皖南地区花岗岩风化壳中稀土元素普遍富集，局部已成为矿床，其中，郎溪县姚村岩体风化壳富集程度较高。LA- ICP- MS锆石U- Pb定年表明，姚村花岗岩体的形成年龄为127. 9±1. 4 Ma，属于皖南地区燕山期晚期岩浆作用的产物。风化壳可细分为残坡积层（A）、强半风化层（C1）、过渡层（C2）、弱半风化层（C3）和基岩（D） 5层。稀土总量在纵向剖面上呈“波浪式”分布，各层稀土分布型式表现出对原岩的继承性。风化壳稀土配分型式与基岩一致， 富集LREE，轻重稀土分馏明显\[(La/Yb)N=15. 6\]，但总含量明显更高。基岩∑REE为338×10-6，半风化层∑REE最高达642×10-6，富集约两倍。风化壳物质由风化残余主矿物（石英、钾长石、斜长石、黑云母）、黏土矿物（高岭石、埃洛石、伊利石、三水铝石等）和副矿物（锆石、磷灰石、榍石等）等组成。黏土矿物以伊利石含量最高，指示风化壳发育不成熟。REE与埃洛石含量明显正相关，与其他黏土矿物关系不明显。（含）稀土矿物（尤其是榍石）对风化壳中稀土元素的贡献量超过 50%，其次为斜长石，是风化壳中REE的重要来源。     

Metavolcanic host rocks,mineralization, and gossans of the Shaib al Tair and Rabathan volcanogenic massive sulphide deposits of the Wadi Bidah Mineral District,Saudi Arabia

The Wadi Bidah Mineral District of Saudi Arabia contains more than 16 small outcropping stratabound volcanogenic Cu–Zn–(Pb) ± Au-bearing massive sulphide deposits and associated zones of hydrothermal alteration. Here, we use major and trace element analyses of massive sulphides, gossans, and hydrothermally altered and least altered metamorphosed host rock (schist) from two of the deposits (Shaib al Tair and Rabathan) to interpret the geochemical and petrological evolution of the host rocks and gossanization of the mineralization. Tectonic interpretations utilize high-field-strength elements, including the rare earth elements (REE), because they are relatively immobile during hydrothermal alteration, low-grade metamorphism, and supergene weathering and therefore are useful in constraining the source, composition, and physicochemical parameters of the primary igneous rocks, the mineralizing hydrothermal fluid and subsequent supergene weathering processes. Positive Eu anomalies in some of the massive sulphide samples are consistent with a high temperature (>250°C) hydrothermal origin, consistent with the Cu contents (up to 2 wt.%) of the massive sulphides. The REE profiles of the gossans are topologically similar to nearby hydrothermally altered felsic schists (light REE (LREE)-enriched to concave-up REE profiles, with or without positive Eu anomalies) suggesting that the REE experienced little fractionation during metamorphism or supergene weathering. Hydrothermally altered rocks (now schists) close to the massive sulphide deposits have high base metals and Ba contents and have concave-up REE patterns, in contrast to the least altered host rocks, consistent with greater mobility of the middle REE compared to the light and heavy REE during hydrothermal alteration. The gossans are interpreted to represent relict massive sulphides that have undergone supergene weathering; ‘chert’ beds within these massive sulphide deposits may be leached wall-rock gossans that experienced silicification and Pb–Ba–Fe enrichment from acidic groundwaters generated during gossan formation.