Mineral Composition of Loess—Paleosol Samples from the Loess Plateau of China and Its Environmental Significance

34samples of loess-paleosol from the Luochuan and Xifeng sections in the Loess Plateau,northern China were eparated into sand,silt and clay fractions and analyzed for their mineral compositions.The results indicate that there is almost no difference between loess and paleosol in mineral composition.Major mineral species are quartz,mica,feldspar and chlorite,accounting for about 88-92% of the total;other minerals are kandite,smectite,vermiculite and a few heavy minerals.The calcite,magnetite and hematite were not taken into consideration because of their removal in the process of sample preparation.The main difference with respect to the mineral composition of samples collected from different sections and different statigraphic levels lies in the amount and grain size of minerals hosted.Comparisons between the Luochuan section and the Xifeng section,between paleosol and loess and between the upper part and the lower part of some paleosol layers show that the formers contain less feldspar but more mica and vermiculite and are finer in grain size,indicating the co-occurrence of both biochemical weathering process responsible for mineral change and physical weathering process leading to grain-size change during the soil-forming processes.This result favours such an explanation of the soil-forming mechanism that loess deposition and paleosol development occurred synchronously,though the rate of soil formation was greater than that of loess deposition,thus leading to soil development.     

Experimental Study on Gold Dissolution from Hosting Minerals of the Hadamengou Gold Deposit and the Implications

The Hadamengou gold deposit is located in western part of the northern margin of the North China craton. It is a hydrothermal deposit related to alkaline magmatism. Dissolution of Au, Fe from pyrite and iron oxide （including magnetite and hematite） individual minerals in the three main types of ore shows： in iron oxides （magnetite and hematite）, Au and Fe were dissolved simultaneously and their solubilities are positively correlated, which means Au is mainly chemical-bonded （lattice gold） and/or colloidal-adsorbed in iron oxides; while in pyrite, on the contrary, Au dissolution obviously lags behind Fe and the solubility of Au shows negative relationship with that of Fe, which indicates Au is mainly hosted as grains of elemental gold （or native gold） within pyrite. Previous studies revealed that the Hadamengou gold deposit is characterized by intensive K-feldspathization and holds high content of iron oxides occasionally replaced by sulfides, which was caused by oxidizing K-enriched alkaline fluids under a stretching geodynamic setting. These geological features, together with the high Au-content in iron oxides, comparable with that of the Olympic Dam deposit in South Australia, suggest that this deposit is the first example of iron oxide-type gold deposits in China.     

论姑山铁矿床的形成条件

On the basis of geological characteristics the Gushan iron deposit should be assigned to volcano-hydruthermal type with hematite qusrtz as its principal mineral assemblage.Iron concentration of the ore-forming fluid has been estimated from the ratio of hematite to quartz in the ores. By using experimental and thermodynamic data the soinbilities of iron minerals at elevated temperatures and pressures are calculated in the system FeO-Fe2O3-NaCl-HCl-H2O. The effect of T, P, pH, fe2 and total concentration of chlorine on the solubilities of iron minerals are discussed. Thermodynamic calculations based on presumed physicochemical conditions for the ore-forming solutions are in good agreement with geological observation. The calculation shows that iron minerals were deposited at log fo2=-21--25, log(mKCl mbl^ ) =-2,5--3, P=1-0.75 (or 0.5) Kb,T=400-350℃. It is believed that the original fluid was an acid NaCl-bearing solution of magmatic derivation. However, iron in the solution was enriched with falling temperature by dissolving pre-exist iron minerals in the consolidated rocks rather than extracted directly from the magma. Either decreasing temperature (below 400℃) or pressure is capable of depositing iron minerals from the solution, but the ratio of Fe to Si in the ore is dependent mainly upon the pH. The widespread silica vein at later stages is a reflection of decreasing acidity of the solution. Increase in fo2 will also favor the deposition of iron minerals. The hypabyssal occurrence and the existance of the Huangmaqing shale contribute greatly to the formation of hematite.     

Study on Composition of Inclusions in Minerals and Simulation Experiment on Hydrothermal Metasomatic Process of the Bayan Obo Iron Deposit

On the basis of the mechanism of formation of mineral inclusions, it may be assumed that a certain relation exists between the compositions of fluid inclusions in various minerals formed at the same stage of hydrothermal activity. In order to study the genetic relationships between different minerals in the Bayan Obo iron deposit, the compositions(K~+, Na~+, Ca~+, Mg~+, F~+, Cl~+, CO_2~(2-), ΣSO_4~(2-) and pH) of inclusions in fluorite(23), hematite(13), magnetite(3), sodium pyroxene(2) and dolomite(5) from the main mine and the eastern mine were determined by using the vacuum decrepitation and leaching methods, and cluster analyses of the data on the compostions were made. The Q-mode cluster analysis indicates that some iron oxide minerals in the deposit are related to dolomite of sedimentary origin, while others are related to fluorite and sodium pyroxene--products of hydrothermal activity. The R-mode cluster analysis shows that the components of the leaching solution may be divided into two groups: one includes CO_2~(2-), Mg~(2+) and H~+(pH), which are obviously associated with dolomite; the other comprises Na~+, K~+, Ca~+, F~+, Cl~+ and SO_4~(2-), which may possibly represent the composition of hydrothermal solutions.The reaction of the Na-F-Cl solution(pH 4.72) with hematite dolomite at 300℃ and 5 × 10~7 Pa and under alternately"static and dynamic" conditions produced large amounts of hematite and fluorite and small amounts of smectite and Na(Fe) silicates, and the hematite-fluorite assemblage accords with the actual geological conditions in the deposit. From a comparison between the compositions of"static" and"dynamic" solution samples, it may be known that the flow reaction facilitates the migration of Fe, F, Ca and other components as well as Na-metasomatism(Na and Si are fixed in a solid phase).The study of the compositions of mineral inclusions and simulation experiments on hydrothermal metasomatism have provided new evidence for the hypothesis of metamorphosed-sedimentary and hydrothermal-remoulding origin of the Bayan Obo deposit, and pointed out emphatically that hydrothermal metasomatism plays an important role in the formation of the mineral deposit, particularly in the main and the east mine.     

Adsorption of Pentachlorophenol onto Oxide and Clay Minerals： Surface Reaction Model and Environmental Implications

The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.     

Mineral Association and Mineralogical Criteria for the Formation Conditions of A B—F—Sn—Bi Skarn in Damoshan,Gejiu Tin Field,Sothwest China

The Damoshan deposit is a small B-F-Sn Bi exoskarn deposit and contains a distinctive mineral assemblage comprising andradite,vesuvianite,calcite,diopside,magnetite,hematite,nordenskioldine,cassiterite,varlamoffite,schenfliesite,native bismuth,eulytite,bismite and bismuthite,in which the occurrence of eulytite is the first reported in China.Textures of the mineral paragenses show that andradite,vesuvianite and diopside were the earliest phases formed during metasomatism,i.e.,the skarn forming stage.Then nordenskioldine,magnetite and native bismuth,perhaps together with eulytite,were precipitated at the stage of retrograde alteration.The minerals varlamoffite,schoenfliesite,hematite ,bismite and bismuthite were probably the product of supergene alteration.The minerals were analyzed by means of electron microprobe.The data on the ,coexisting phases and their compositons show that during the metasomatism reduced F-and Sn-rich primary mineralizing solutions reacted with highly oxidized carbonated of the Gejie Formation,producing a high Fe^2 /Fe^3 skarn(vesuvianite-fluorite skarn)near the contact of granite,and a low Fe^2 /Fe^3 skarn(vesuvianite-fluorite skarn)near the contact of granite,and a low Fe^2 /Fe^3 skarn(andradite skarn)in the outer zone of the skarn body in which andradite is extremely tin-bearing up to 5.14 wt% SnO2),In the retrograde alteration stage ,B-rich,but F-and Si-deficient mineralizing solutions replaced the tin-bearing andradite,forming an association of nordenskioldine and magnetite,No sulphides were deposited at this stage because of the oxidization ambient conditions in the andradite skarn.In the spergene oxidation zone,the nordenskioldine was dissolved into varlmoffite and calcite,the native bismuth was transformed into bismite or bismuthite ,and the magnetite was altered into hematite under the action of the CO2-rich supergene solutions.     

混合花岗岩的成因及其与铁矿关系的实验研究

Experiments have been conducted over a wide range of temperature and pressure(300--950℃, 500--2000 bars) in attempting to gain some better understanding of the geological features of Precambrian migmatite granite and banded iron formation (BIF)widespread in Northeast China. Results indicate that BIF of Anshan type is unstable under the action of sufficient alkaline solutions with some iron or aluminum silicates formed at the expense of quartz. Rock melting experiments show that the beginningof-melting temperatures of phyllite, biotite plagioclase gneiss and migmatite granite range from 680 to 640℃, but that of BIF and plagioclase amphibolite are 150-200℃ higher. The authors suggest that migraatite in this region has been resulted from partial melting and metasomatizm. With respect to the relation between migmatization and iron deposits, it has been experimentally revealed that migmatite will not “digest” the BIF if they are separated by other country rocks. But melting to various extent will take place in BIF where migmatite is in direct contact with it. Additionally, the BIF will even become richer in iron under favorable conditions. This information may probably help in guiding our efforts to prospect for Precambrian iron deposits in. regions with extensive occurrence of migmatite.     

A Textural and Mineralogical Study of the Shanzhuang Banded Iron Formation, Southeastern Margin of the North China Craton: Implications for the Overprint History of Hydrothermal Alteration and Supergenesis after Mineralization

The newly discovered Shanzhuang BIF is hosted in the Shancaoyu Formation of the Taishan Group within the Eastern Block, southeastern margin of the North China Craton. The ores can be subdivided into three types in terms of mineral assemblages, corresponding to three types (I, II, III). The element concentration of the type I magnetite is similar to that of the type II magnetite, while the type III magnetite is similar to that of the schist. In general, magnetite and hematite grains from the ores show high concentrations of Mn (1317, 1162 ppm), Co (787, 1023 ppm), Al (2224, 2435 ppm) and Ti (540, 300 ppm), Whereas magnetite is depleted in Si (420 ppm) and hematite enriched in Si (1690 ppm). Detailed petrographic and mineral chemical analysis of magnetite, hematite, amphibole/hornblende and pyroxene, reveals that almost all the minerals occur as subhedral-anhedral grains with pits and fractures, and the BIF is recrystallized to metamorphic assemblages of high amphibolite facies. Hornblende is highly enriched in Fe, Mg and Ca, but depleted in K and Na, mostly belonging to magnesiohornblende. In addition, the ratios of Mg/(Mg+Fe2+), Fe3+/(Fe3++Fe2+), Si/(Si+Ti+Al) and Al/Si are 0.48–0.64, 0.17–0.36, 0.79–0.88 and 0.14–0.27, respectively. It is suggested that hornblende is neither a typical magmatic origin nor a typical metamorphic. Pyroxene has the characteristics of high Ca and Fe, but low Ti and Al, with end-member components En, Wo and Fs in the ranges of 25.22–28.64 wt%, 43.71–46.40 wt% and 24.51–27.62 wt%, respectively, belonging to clinopyroxene, and mostly diopside, might be formed during the prograde metamorphism in the absence of H2O. The carbonate such as dolomite-ankerite series is probably a precursor mineral of the BIF deposit. Mass mineral chemical and structural characteristics indicate that the Shanzhuang iron deposit has been subjected to varying degrees of oxidized hydrothermal superimposed reformation, metamorphism, and supergenesis after mineralization, during which some elements have been migrated in some degree.     

Ferrimagnetic minerals in red paleosols of Pleistocene Epoch, eastern China

The type,grain size and origin of ferimagnetic minerals separated from red paleosols of pleistocene Epoch(Q2)in eastern China ,were studied by using mineral magnetic measurement,X-ray powder diffraction and electron microscopy.Results showed that the iron oxider in red paleosols were composed of hematite(α-Fe2O3),maghemite(γ-Fe2O3) and goethite(α-FeOOH),Mineral magnetic parameters and X-ray diffraction patterns indicated that maghemite was the dominant remanence carrier in red paleosols,which is characterized by superparamagnetic(SP) and stable single domain(SSD) grains,The variations of magnetic susceptibility(χ） ,anhysteretic magnetic susceptibility(χRAM）and saturation isothermal remanent magnetization(SIRM) for red paleosols following heating to various temperatures showed two peak values at 700℃ and 900℃.The spherulitic magnetic particles measuring 250-1000μm in diameter in red paleosols were separated by the magnetic separation method,indicating that these magnetic particles were an assemblage of superparamagnetic and stable single domain ferrimagnetic grains,It is suggested that the ferrimagnetic minerals of red paleosols be a pedogenic ferrimagnetic component under high temperature and high humid conditions in the Pleistocene Fpoch(Q2).It is concluded that the magnetism characteristics of red paleosols can be used to evaluate the environmental changes of Quaternary in eastern China.     

Forms of Iron in the Phosphorites of Abu—Tartur Area,Egypt

The Campanian-Maastrichtian phosphatic deposits in Egypt,called the Duwi Forma-tion,comprise a part of the extensive Middle East to North African phosphogenic province of Late Cretaceous to Paleogene age.The province holds the greatest accumulation of phosphorites in the geological history,possibly in excess of 70 billion metric tons.The phosphate resources in Egypt alone exceed 3 billion metric tons.Two-third of these three billions occur only in the Abu-Tartur area.Among the phosphorite deposits in Egypt,the phosphorites of the Abu-Tartur area are characterized by high contents of iron ranging from 3% to 7% with an average of 5%.The detailed mineralogical and geochemical studies on the Abu-Tartur phosphorites revealed that iron is found in the form of pyrite,ankerite,clay minerals,microinclusions,and iron oxide.Pyrite,which is the major fraction,occurs as filling cement and partial to complete teplacement of phosphatic grains and confined to the fresh phosphorites while iron oxide occurs as cryp-tocrystalline aggregates of red to brown particles and is confined to the weathered outcrops.Ex-clusive relations between pyrite in the fresh phosphorite samples inside the Abu-Tartur mine and iron oxide in the equivalent horizon of the weathered exposure indicated that iron oxide was formed by the oxidation of pyrite as a result of weathering.All of these forms harm the quality of ore,manufacturing processes,and the produced phosphoric acid and fertilizers.     

Mechanism and kinetics of hydrothermal replacement of magnetite by hematite

The replacement of magnetite by hematite was studied through a series of experiments under mild hydrothermal conditions(140 -220℃, vapour saturated pressures) to quantify the kinetics of the transformation and the relative effects of redox and non-redox processes on the transformation. The results indicate that oxygen is not an essential factor in the replacement reaction of magnetite by hematite, but the addition of excess oxidant does trigger the oxidation reaction, and increases the kinetics of the transformation. However, even under high O_2(aq) environments, some of the replacement still occurred via Fe²⁺ leaching from magnetite. The kinetics of the replacement reaction depends upon temperature and solution parameters such as pH and the concentrations of ligands, all of which are factors that control the solubility of magnetite and affect the transport of Fe²⁺ (and the oxidant) to and from the reaction front. Reaction rates are fast at ~200℃, and in nature transport properties of Fe and,in the case of the redox-controlled replacement, the oxidant will be the rate-limiting control on the reaction progress. Using an Avrami treatment of the kinetic data and the Arrhenius equation, the activation energy for the transformation under non-redox conditions was calculated to be 26 ± 6 kJ mol^-1.This value is in agreement with the reported activation energy for the dissolution of magnetite, which is the rate-limiting process for the transformation under non-redox conditions.     

Mineralogy, geochemistry and release of heavy metals in wastes from indigenous zinc smelting in Northwest Guizhou

Environmental impact resulting from mining activities is serious and ubiquitous all over the world, and it has become one of the important aspects in environmental geochemistry. The environment was seriously damaged by wastes from historical zinc smelting in Northwest Guizhou. The geochemical distributions of Pb and Zn in the different grain-size fractions of wastes indicate that the coarser particles show similar or even higher heavy metal concentrations than finer ones in the samples, although the concentrations of heavy metals tend generally to increase as the size fractions get finer. The heavy metal contents are very high, with maximum values of 31631, 57178, 2367 and 311.5 mg/kg for Pb, Zn, Cu and Cd, respectively. It is also shown that the residual fraction of Pb is less than that of Zn, accounting for 0.39%-15.75% and 14.3%-46.2%, respectively, of the total, and this is likely relative to Zn-silicate minerals formed from smelting. Although the relative partitioning of Pb and Zn is very low （0.03%- 1.3.% for Pb; 0.03% -3.3% for Zn）, the exchangeable fraction of the waste contains large amounts of heavy metals （1.5%-385 μg/g for Pb; 3-590 μg/g for Zn）. Heavy metals in exchangeable forms have the highest solubility to give the highest potential bioavailability in contrast to other chemical forms. Mineralogical study indicates that the wastes were found to be highly heterogeneous materials, dominated by quartz, feldspar, carbonatite, iron or/and aluminum vitric compounds and a few secondary mineral phases, and their contents vary with the type of smelting wastes. The secondary minerals formed from smelting and sequentially weathering are the major chemical phase for heavy metals. Complex composition of many phases and substitution of elements suggested that many of the phases were found to be non-stoichiometric compounds. Pb was found to be the main Pb phase in the wastes by precipitation or/and adsorption.     

Reactions between olivine and CO_2-rich seawater at 300℃:Implications for H_2 generation and CO_2 sequestration on the early Earth

To understand the influence of fluid CO_2 on ultramafic rock-hosted seafloor hydrothermal systems on the early Earth,we monitored the reaction between San Carlos olivine and a CO_2-rich NaCl fluid at 300 C and 500 bars.During the experiments,the total carbonic acid concentration(∑XO_2) in the fluid decreased from approximately 65 to 9 mmol/kg.Carbonate minerals,magnesite,and subordinate amount of dolomite were formed via the water-rock interaction.The H_2 concentration in the fluid reached approximately 39 mmol/kg within 2736 h,which is relatively lower than the concentration generated by the reaction between olivine and a CO2-free NaCl solution at the same temperature.As seen in previous hydrothermal experiments using komatiite,ferrous iron incorporation into Mg-bearing carbonate minerals likely limited iron oxidation in the fluids and the resulting H_2 generation during the olivine alteration.Considering carbonate mineralogy over the temperature range of natural hydrothermal fields,H_2 generation is likely suppressed at temperatures below approximately 300℃ due to the formation of the Mg-bearing carbonates.Nevertheless,H_2 concentration in fluid at 300℃ could be still high due to the temperature dependency of magnetite stability in ultramafic systems.Moreover,the Mg-bearing carbonates may play a key role in the ocean-atmosphere system on the early Earth.Recent studies suggest that the subduction of carbonated ultramafic rocks may transport surface CO_2 species into the deep mantle.This process may have reduced the huge initial amount of CO_2 on the surface of the early Earth.Our approximate calculations demonstrate that the subduction of the Mg-bearing carbonates formed in komatiite likely played a crucial role as one of the CO_2 carriers from the surface to the deep mantle,even in hot subduction zones.     

Leachate Lithium Characteristics of Loess-paleosol Sequences on the Chinese Loess Plateau and their Paleoclimatic Significance

The geochemical components of the leachate from loess-paleosol deposits can provide information about climate-related post-depositional processes. For example, leachate lithium ([Li]leachate) is a potential paleoclimate proxy because lithium is a typical lithophile element that is readily adsorbed by clay minerals during weathering and pedogenesis, and thus stratigraphic variations in [Li]leachate can reflect these processes. We investigated the [Li]leachate values of two loess-paleosols profiles (the Luochuan and Weinan sections), on a north–south climatic gradient on the Chinese Loess Plateau. Independent paleoclimate information was provided by measurements of magnetic susceptibility, grain size, Rb/Sr ratios, and clay mineral content. During the last glacial-interglacial period, [Li]leachate increased from 0.39 to 1.97 μg/g at Luochuan and from 0.67 to 2.45 μg/g at Weinan, mainly due to increasing pedogenesis. Based on these results we developed a conceptual model to explain the variations in [Li]leachate. Li+ within loess layers is mainly derived from dust input and the decomposition of primary minerals, influenced by the East Asian winter monsoon, while in paleosol layers Li+ is mainly derived from clay mineral adsorption during pedogenic processes, influenced by the East Asian summer monsoon.     

Major and Trace Elements of Magnetite from the Qimantag Metallogenic Belt: Insights into Evolution of Ore–forming Fluids

Magnetite, as a genetic indicator of ores, has been studied in various deposits in the world. In this paper, we present textural and compositional data of magnetite from the Qimantag metallogenic belt of the Kunlun Orogenic Belt in China, to provide a better understanding of the formation mechanism and genesis of the metallogenic belt and to shed light on analytical protocols for the in situ chemical analysis of magnetite. Magnetite samples from various occurrences, including the ore–related granitoid pluton, mineralised endoskarn and vein–type iron ores hosted in marine carbonate intruded by the pluton, were examined using scanning electron microscopy and analysed for major and trace elements using electron microprobe and laser ablation–inductively coupled plasma–mass spectrometry. The field and microscope observation reveals that early–stage magnetite from the Hutouya and Kendekeke deposits occurs as massive or banded assemblages, whereas late–stage magnetite is disseminated or scattered in the ores. Early–stage magnetite contains high contents of Ti, V, Ga, Al and low in Mg and Mn. In contrast, late–stage magnetite is high in Mg, Mn and low in Ti, V, Ga, Al. Most magnetite grains from the Qimantag metallogenic belt deposits except the Kendekeke deposit plot in the " Skarn " field in the Ca+Al+Mn vs Ti+V diagram, far from typical magmatic Fe deposits such as the Damiao and Panzhihua deposits. According to the(Mg O+Mn O)–Ti O2–Al2O3 diagram, magnetite grains from the Kaerqueka and Galingge deposits and the No.7 ore body of the Hutouya deposit show typical characteristics of skarn magnetite, whereas magnetite grains from the Kendekeke deposit and the No.2 ore body of the Hutouya deposit show continuous elemental variation from magmatic type to skarn type. This compositional contrast indicates that chemical composition of magnetite is largely controlled by the compositions of magmatic fluids and host rocks of the ores that have reacted with the fluids. Moreover, a combination of petrography and magnetite geochemistry indicates that the formation of those ore deposits in the Qimantag metallogenic belt involved a magmatic–hydrothermal process.     

Sodium-rich volcanic rocks and their relationships with iron deposits in the Aqishan-Yamansu belt of Eastern Tianshan,NW China

The volcanic rocks hosting the iron deposits in the Aqishan–Yamansu metallogenic belt are sodium-rich.The geochronology,petrography,and geochemistry of minerals and sodium-rich rocks as well as the relationship between these rocks and the iron deposits are studied.Geochemically,the ore-hosting volcanic rocks are sodiumrich(the averages of Na2O and Na2O/K2O are 4.31 wt.%and 8.56,respectively)and belong to the calc-alkaline series.They are enriched in LREEs and LILEs(Ba,U,K,and Sr),but depleted in HFSEs(Nb,Ta,and Ti).SHRIMP zircon U–Pb dating of the crystal tuff in the Aqishan Formation and the dacite in the Tugutu Bulak Formation yields ages of 337.5
2.3 Ma(n?15,MSWD?0.85)and 313.0
3.3 Ma(n?13,MSWD?0.74),respectively,indicating that the sodium-rich volcanic rocks formed from the early–late Carboniferous.Electron microprobe data from plagioclases demonstrate that albites and/or oligoclases were formed in the basic–intermediate–acid volcanic rocks.Two stages of albitization are identified,and the latter is likely attributed to the dissolution of iron in the Aqishan–Yamansu belt.The sodium-rich volcanic rocks probably formed by the interaction between volcanic lava and seawater after volcanoes erupted on the seafloor;meanwhile,the albites formed by element substitution in a low-metamorphic environment.The spatiotemporal coupling relationship between sodium-rich volcanic rocks and iron deposits in the Aqishan–Yamansu belt is favorable.Iron dissolved from the dark minerals of basic–intermediate volcanic rocks through sodium metasomatism is one of the material sources for the iron deposits.     

辽宁鞍本地区弓长岭型富铁矿成矿的垂直分带

The high-grade iron deposits of the Gongchangling type occur in the Archaeozoic Anshan Group of this region and are classified as stratabound deposits. They underwent stages of sedimentation, regional metamorphism, and hydrothermal enrichment during the course of formation. Hydrothermal enrichment is notable in the vertical zoning pattern, i.e., from the bottom upwards, zone A hlgh-grade magnetite ore; zone B low-grade magnetite ore; zone C transition zone between hematite and magnetite ore ; zone D low-grads hematite ore ; zone E alterated cover. Through the vertical profile of the orebody, regular variations can be recognized in iron concentration, in the characteristics of country rock alteration, the ore-controlling structure and the properties of the hydrothermal ore-forming fluids. A two-fold source, deep hot brines and shallow thermal groundwater, is suggested for the origin of the ore-formlng hydrothermal fluids. The two fluids, mixed in varying proportions, are responsible for the various geochemical reactions during the course of ascending, exerting controls on the iron content of ore and the pattern of vertical zonation. A better understanding of the vertical zonation is expected to shed light on the exploration for such type of ore deposits.     

The erosion-weathering link： New insights from the sediment geochemistry of Himalayan small catchments？

The causal links between physical erosion and chemical weathering remain poorly constrained, despite their importance for understanding landscape evolution, nutrient supply for ecosystem development, and the quantitative impact of tectonic uplift on the long-term carbon cycle and Earth＇s climate. This is partly because weathering processes are particularly complicated at high erosion rates, where there are a variety of controlling parameters. The Himalayas provide an ideal natural laboratory for studying weathering processes across an environmental gradient undergoing rapid erosion. We have previously used solute budgets to determine weathering rates in small catchments in the High Himalayas and Middle Hills of central Nepal. In-situ weathering rates are highest in the warmer Middle Hills, while the total riverine budgets suggest that much of the weathering of High Himalayan material must occur after erosion, during transport through the Ganges Plain （West et al., 2002）. Here, we will present new data on the geochemistry of the solid phase （soils and sediments） from these small Himalayan catchments, including time constraints from U-series analysis. This will provide information about the residence time of material in the weathering environment, and its relation to weathering rates.     

Formation and Evolution of a Paleosol across the Lower Silurian-Lower Permian Boundary in Zunyi District, Northern Guizhou, China and Its Paleoenvironment and Paleoclimate Implications

This paper presents a set of bulk geochemical and mineralogical data from a paleoweathering profile located in Zunyi District, Northern Guizhou, China. It was formed at the top of the Hanjiadian Formation of the Lower Silurian. A truncated, argillic, gleyed, kryptic paleospodosol is recognized in the paleoweathering profile. Ratios of immobile elements (Ti/Zr, Ti/Al) and their binary (e.g., Nb vs. Zr/TiO2 and Th/Sc vs. Zr/Sc), triangular diagrams (La-Th-Sc, Th-Sc-Zr/10, Zr-Cr-Ga) reflect that the Gaojiayan paleosol is the product of in-situ weathering of gray-green silty mudstone of the underlying Hanjiadian Formation. Mass balance calculations indicate K enrichment and Na enrichment in the upper and lower portions of paleosol, respectively. These findings both are the results of transgression, which brings substantial concentrations of such elements as K, Na, and Sr. In particular, K enrichment is achieved by the illitization of kaolinite. The biological processes of terrestrial vascular plants also enhance K concentration, especially at the top of the paleosol. Na enrichment is a consequence of albitization and/or adsorption by clay minerals through cation exchange. The mass distributions and relative mass changes of rare earth elements (REEs) in the studied profile display characteristics of vertical zonation. Three peaks in total REEs content are observed, indicating two paleoclimatic or paleoenvironmental changes. Mineralogical characteristics indicate that the paleoclimate changed first from warm and humid to cold and dry and later, to dry and lightly warmer. The corresponding soil environment varies from weakly acidic to strongly alkaline and later, to weakly acidic. Mass translocation characteristics of REEs and several transition metals suggest that the Gaojiayan paleosol may have undergone top erosion.     

Burial Records of Reactive Iron in Cretaceous Black Shales and Oceanic Red Beds from Southern Tibet

One of the new directions in the field of Cretaceous research is to elucidate the mechanism of the sedimentary transition from the Cretaceous black shales to oceanic red beds. A chemical sequential extraction method was applied to these two types of rocks from southern Tibet to investigate the burial records of reactive iron. Results indicate that carbonate-associated iron and pyrite are relatively enriched in the black shales, but depleted or absent in red beds. The main feature of the reactive iron in the red beds is relative enrichment of iron oxides （largely hematite）, which occurred during syn-depostion or early diagenesis. The ratio between iron oxides and the total iron indicates an oxygen-enriched environment for red bed deposition. A comparison between the reactive iron burial records and proxies of paleo-productivity suggests that paleo-productivity decreases when the ratio between iron oxides and the total iron increases in the red beds. This phenomenon could imply that the relationship between marine redox and productivity might be one of the reasons for the sedimentary transition from Cretaceous black shale to oceanic red bed deposition.