M1 site splitting due to Next Nearest Neighbor effects and ferric iron in tetrahedral site in clinopyroxene megacrysts

It is well known that in pyroxene structure,there are two metal sites,M1 and M2.Generally speaking,Ferrous iron in each of these sites would normally be expected to give rise to a doublet,However,anomalies have been found in the relative areas of the peaks in the room temperature spectra of some clinopyroxene(CPX)when the above assignment is followed.According to the calculation of Next Nearest Neighbor configurations of divalent cations in M1,we found that the four configurations of M1 can be divided into two groups.One group is 3Ca configuration that increases with the content of Ca(p.f.u);the other group is made up of three No-3Ca configurations that decrease with the content of Ca.The two groups contribute to the spectrum structure of M1.so in this study we fit two doublets for ferrous iron in M1.Though there were several reports on Fe^3 in tetrahedral site previously,it was not sure that Fe^3 occupies the T site is a universal fact in CPX,despite of the content of Al.We found that the Fe^3 in the T site fitted by Moessbauer spectroscopy is negatively correlated to the Si content in the T site and positively correlated to the Fe^3 in the T site estimated on the supposition that Fe^3 and Al occupy the T site randomly.If it is true.it is important in the modeling of ion exchange geobarometries and geothermomeries.     

月岩（70017—291）的X光电子能谱（XPS）初步研究

Using X-ray photoemission spectroscopy (XPS), the Preliminary results on the lunar basalt sample (70017-291)are shown in the paper. Major elements (O, Si,Al, Fe, Ca, Mg, Ti, etc.) of the lunar sample are similar to that of the Jilin meteorite and the Allende meteorite. The valence of iron in the sample has also been studied in detail. The authors suggest that Fe^ may be differentiated from Fe^ in the XPS spectra in terms of the satellite lines of Fe(2p3/2).     

Geochemical studies on Dachang antimony ore deposit in Qinglong, Guizhou Province

The Dachang antimony deposit in Qinglong,Guizhou Province,is strictly controlled by the “Dachang Layer” which is a complex altered rock occurring at unconformity between the Permian Emeishan basalt and the Maokou limestone.Based on the studies of the hanging-and foot-wall rocks,the trace elements and REE contents of the rocks and ores and heavy placer minerals in the basalt,this paper is focused on the relations between these data and the “Dachang Layer”and its hanging- and oot-wall rocks.The author pointed out that the “Dachang Layer” and basalt are the source-beds of antimony;ilmenite and magnetite are the major mineral carriers of antimony.In the processes of halmyrosis and burial metamorphism of the “Dachang Layer” an basalt,antimony was mobilized along with the mobilization of iron and was preliminarily concentrated in the“ Dachang Layer”.     

阿波罗-17（70017-291）高钛月海玄武岩的化学组成及其成因的探讨

Chemical, petrological and mineralogical studies on 70017-291 Mare basalt indicate that the mare basalt belongs to Type B of A-17 basalts with a texture of plagioclasepoikilitic ilmenite basalt. The mean chemical composition of this basalt is as follows:SiO2 39.01, TiO2 11.32, Al2O3 9.24, FeO 18.52, MgO 8.61, CaO 10.86 (%). INAA measurements were made on the basalt for major, minor and trace elements. Seven pyroxene grains in the Apollo 17 were also analyzed by microprobe. They show two compositions, one for pigeonite, and the other for augite-subcalicaugite. The mean composition of pigeonite is Wo10.85, En59.33 Fs30, and that of augite-subcalic augite Wo25 En41.5Fs38.3. Plagioclase grains have a composition ranging from An30 to An96. The plagioclase contains detectable iron (averaging 0.74%), potassium (0.089% in average) and titanium(averaging 0.16%). The mean composition of ihnenite is TiO2 53.98%, FeO 41.02%,Al2O3 0.21%, MgO 2.41%, Cr2O3 0.74%. The Ti-high mare basalt (70017-291) was formed by partial melting of the early cumulates through assimilation and migmatization. On the whole, mare basalts seem to be of multigenesis.     

Screening Effect of the Diffusive Boundary Layer in Sediments of Lake Aha in the Suburbs of Guiyang City,Guizhou Province

The redox cycle of iron and manganese is a major geochemica process at the boundary layers of lake sediments.Lake Aha,which lies in the suburbs of Guiyang City,Guizhou Province,China,is a medium-sized artificial reservoir with seasonally anoxic hypolimnion,Long-term sedimentary accumulation of iron and manganese resulted in their enrichment in the upper sediments,In the anoxic season,Fe^2 and Mn^2 ,formed by diological oxidation,would diffuse up to overlying waters from sediments.However,the concentration of oxidation,would diffuse up to overlying waters from sediments,However,the concentration of Fe^2 increased later and decreased earlier than that of Mn^2 .Generally,sulfate reduction occurred at 6 cm below the sediment-water interface.Whereas,in the anoxic season.the reduction reached upper sediments,inhibiting the release of Fe^2 ,The Fe concentration of anoxic water is quickly decreased from high to low as a result of reduction of the suplhur system.     

Depth of volcanic basalt degassing forecasted from CO2 fluid inclusions

Fluid inclusions have recorded the history of degassing in basalt. Some fluid inclusions in olivine and pyroxene phenocrysts of basalt were analyzed by micro-thermometry and Raman spectroscopy in this paper. The experimental results showed that many inclusions are present almost in a pure CO2 system. The densities of some CO2 inclusions were computed in terms of Raman spectroscopic characteristics of CO2 Fermi resonance at room temperature. Their densities change over a wide range, but mainly between 0.044 g/cm3 and 0.289 g/cm3. Their micro-thermometric measurements showed that the CO2 inclusions examined reached homogenization between 1145.5℃ and 1265℃ . The mean value of homogenization temperatures of CO2 inclusions in basalts is near 1210℃. The trap pressures (depths) of inclusions were computed with the equation of state and computer program. Distribution of the trap depths makes it know that the degassing of magma can happen over a wide pressure (depth) range, but mainly at the depth of 0.48 km to 3.85 km. This implicates that basalt magma experienced intensive degassing and the CO2 gas reservoir from the basalt magma also may be formed in this range of depths. The results of this study showed that the depth of basalt magma degassing can be forecasted from CO2 fluid inclusions, and it is meaningful for understanding the process of magma degassing and constraining the inorganogenic CO2 gas reservoir.     

High precision Fe isotope measurement and applications in aquatic environmental studies

In aquatic environment, iron redox reaction may occur through a） microbial activity and b） photo-chemistry. Iron chemistry plays a significant role in the health of aquatic ecosystems. For example, Fe^2＋ is more mobile than Fe^3＋. Iron can be bound to dissolved organic carbon （DOC）, and when Fe^2＋ is oxidized to Fe^3＋ （biotically or abiotically）, Fe is precipitated and induce co-precipitation of the DOC. Furthermore, iron is a major nutrient to aquatic organisms. Because Fe^2＋ is more bioavailable than Fe^3＋, iron redox chemistry can be a controlling factor in biological production, such as algae bloom which can be a public health concern. Experiments have shown that Fe redox reactions, biotically or abiotically, can generate significant Fe isotope fraction among different Fe species. Accordingly, analysis of Fe isotope composition of phytoplanktons can be a valuable tool in studying Fe dynamics in ecosystems. Precise measurement of Fe isotope, however, presents some challenges. Recent advances in mass spectrometry, specifically high resolution MC-ICP-MS, allow measurement of Fe isotopes free of interferences.     

Moessbauer and XRD characterization of contaminated sediments by coal mining drainage in Neath Canal, South Wales, UK

Sediment cores were collected from the upstream of the Neath Canal in South Wales and characterized for their mineral compositions and iron speciation in order to understand the influence of sedimentary properties on the contaminants of heavy metals. The sediments in the canal have been polluted by ocherous precipitate with heavy metals such as arsenic since a major mine water discharge in spring 1993. The sediment core was obtained just from the discharge point in the canal and distinguished into three layers in the field regarding to their physical properties including visible color, sediment particle composition and dryness. X-ray diffraction （XRD） and M6ssbauer spectroscopy revealed vertical variations of minerals and iron species in depth of the sediment profile. The upper layer, reddish-brown, is wet muddy precipitant and is very fine in particle size, consisting mainly of iron oxide and hydroxide. Arsenic is rich in this layer; probably the sorption on iron oxide surface is the main mechanism. The middle layer, 22.0-27.0 cm, is soft deposit in a yellow color and contains sheet silicate, calcite and goethite. The lower part below 27.0 cm is gray to dark gray in color and contains quartz, pyrite, coal particles that are much more similar to normal aquatic sediment. The upper two layers in brown and yellow colors as newly precipitated mud from AMD contain high concentrations of As, Ni under oxic conditions. The lower part as the old canal sediments under reducing conditions contains high Cu and Zn. Chromium is enriched in the limited part of the low layer, just beneath the boundary between the middle and low parts of the sedimentary column, where the redox conditions shifted from oxic to anoxic. It is clear that the distribution of these heavy metals is closely associated with the redox condition reflected in the iron speciation. Thus different treatments are necessary for each layer of the sediment since different mineral and geochemical properties of the sediment will give different impacts on the heavy metals.     

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.     

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.     

Geochemistry and Tectonic History of Seamount Remnants in the Xingshuwa Subduction Accretionary Complex of the Xar Moron Area,Eastern Margin of the Central Asian Orogenic Belt

This study focuses on the geology, geochemistry, zircon U-Pb geochronology and tectonic settings of the three types of seamount basalts from the Xingshuwa subduction accretionary complex in the Xar Moron area, eastern margin of the Central Asian Orogenic Belt(CAOB). The seamount remnants are composed of carbonate 'cap' sediments, large volumes of pillow and massive basalts, carbonate breccia slope facies and radiolarian cherts. Group 1 basalts are characterized by high contents of P2 O5 and TiO2 with alkaline affinity and LREE enrichment, indicating that they are derived from intraplate magma. Group 2 basalts display N-MORB LREE depletion patterns, indicating that they were formed at a mid-ocean ridge. Group 3 basalts have shown distinct Nb depletion and high Th/Yb ratios, indicating that they were generated in an island arc tectonic setting. The zircon U-Pb age of Group 1 basalt sample XWT18-131 is 576.4 ± 9.4 Ma, suggesting that the oceanic island seamount was the product of intraplate magmatism related to a mantle plume or 'hot spot' in the late Neoproterozoic. The zircon U-Pb age of Group 2 basalt sample XWT18-132 is 483 ± 22 Ma, indicating that the Paleo-Asian Ocean(PAO) was continuously expanding in the Early Ordovician. The zircon U-Pb age of Group 3 basalt sample XWT18-101 is 240.5 ± 8.2 Ma, suggesting that this area underwent the evolutionary path of ocean-continent transition, developing towards continentalization during the Middle Triassic. Thus, we believe that there was both mantle plume-related intraplate magmatism and intraoceanic subduction during the evolution of the PAO, the CAOB possibly being an evolutionary model of an intraoceanic subduction and mantle plume magmatism complex.     

包裹体研究与石碌铁矿成因的探讨

Shilu iron deposit is one of the highly economically important rich iron deposits in China. Based upon the research results on its ore composition and fluid inclusions, it can be reasonably explained that the genesis of this iron deposit is such that marine voleanic sediments there suffered later regional metmnorphism and hydrothermal reformation. The temperature of regional metamorphism ranges from 465 to 536℃,while that of hydrothermal reformation from 344 to 396℃. The latter seems to be related to the migmatization of Zhan Xian stock near Shilu iron deposit, Due to the hydrothermal reformation, the ore-forming materials were mobilized and transfered from the marine sedimentary rocks, subsequently redepositing and concentrating as a rich iron deposit in the present site.     

Study on the Tectonic Setting for the Ophiolites in Xigaze, Tibet

The Xigaze ophiolite is located in the middle section of the Yarlung Zangbo River ophiolite belt and includes a well-preserved sequence section of seven ophiolite blocks. The relatively complete ophiolitic sequence sections are represented by Jiding, Dejixiang, Baigang, and Dazhuqu ophiolites and consist of three–four units. The complete ophiolite sequence in order from the bottom to top consists of mantle peridotite, cumulates, sheeted sill dike swarms, and basic lavas±radiolarian chert. These cumulates are absent in the remaining blocks of Dejixiang and Luqu. The age of radiolaria in the radiolarian chert is Late Jurassic–Cretaceous. The basalt and ultramafic rock of the ophiolite also are overlaid by Tertiary Liuqu conglomerate, which contains numerous pebble components of ophiolite, indicating that the Tethys Ocean began to close at the end of Cretaceous Period. The isotopic data of gabbro, diabase, and albite granite in the Xigaze ophiolite are approximately 126–139 Ma, which indicates that the ophiolite formed in the Early Cretaceous. The K–Ar age of amphibole in garnet amphibolite in the ophiolite mélange is 81 Ma, indicating that tectonic ophiolite emplacement occurred at the end of Late Cretaceous.     

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.     

沉积岩中镁钠闪石石棉矿物的初步研究

Alkali amphibole asbestus is widely distributed in a Mesozoic terrestrial redbed.Preliminary mineralogical study shows that it belongs to magnesian riebeckite asbestus. The mineral contains higher Na, Mg and Fe^3 , lower Al, and is well comparable with that of typical magnesian riebeckite asbestus in chemical composition. A comparasion between the methods used for calculating the crystallochemical formula of amphibole indicatesthat the structural characteristics of amphibole can be best brought out if a total catian number of 15, i.e., x y z=15, is taken as the factor for magnesian riebeckite. The infrared spectra for fibrous magnesian riebeckite exhibit two definite absorption bands. The firat one is at 850--1250 cm^-1, involving several minor bands due to the valency vibration of Si--O, with maximum values of 975,1025, 1080cm^-1 respectively. The second absorption band which is attributable to the distortional vibration of Si--O--Si, is detected at 350--600cm^-1, with a maximum value of 440cm^-2. Optically, its refractien iadices bacrease with increasing transition elements, especiany the ratio of Mg/Mg Fe^2 Fe^3 Mn. A distinct exothermic effect is observed between 350--400℃, indicating the oxidation of Fe^3 to Fe^3 . A deep endothermic valley between 970--1020℃ can be attributed to the melting of magnesian riebeckite and the formation of new minerals. The auther oonsideres that fibrous magnesian riebeckite is crystallized in favorable accumulation strata from a Na-, Mg-, Fe-rich silicate colloidal solution that has been derived from country rocks by some alkline ground water duringg the process of sedimentation and diagenesis in terrestrial saline carbonate muds. Magnesian riebeckite formed at terrestrial carbonate saline formations promises to be a potentially important genesis type for alkali amphiboles.     

Effects and mechanism of igneous rock on selenium in the tropical soil-rice system in Hainan Province,South China

To illuminate the migration and transformation of selenium(Se)in the igneous rock-soil-rice system,285 pairs of rhizosphere soil and rice samples were collected from the granitoid and basalt areas in Hainan Province,South China.The contents of Se in soils derived from granitoid and basalt are,respectively,0.19±0.12 mg/kg and 0.34±0.39 mg/kg,which are much higher than Se contents in granitoid and basalt.Selenium shows remarkable enrichment from granitoid and basalt to soils.The mobile fraction of Se in soils derived from granitoid is 0.0100±0.0034 mg/kg,which is significantly higher than that of basalt(0.0058±0.0039 mg/kg).Although soil derived from basalt shows higher Se contents,Se contents in rice samples,mobile fractions of Se in soils,and biological concentration factor(BCF)is similar or even lower than that from granitoid.Basalt consist of calcic plagioclase and pyroxene,and are much richer in Fe,Al,and Ca than granitoid.Correspondingly,the basalt-derived soils have higher goethite,hematite,kaolinite,cation exchange capacity(CEC)content,and higher p H than the granitoid-derived soils,which result in higher adsorption capacity for Se and relatively lower Se bioavailability.Soils derived from granitoid and basalt in tropical regions are beneficial to produce Se-rich rice.     

Opaque Mineralogy as a Tracer of Magmatic History of Volcanic Rocks:an Example from the Neogene-Quaternary Harrat Rahat Intercontinental Volcanic Field, North Western Saudi Arabia

The Neogene-Quaternary Harrat Rahat volcanic field is part of the major intercontinental Harrat fields in western Saudi Arabia.It comprises lava flows of olivine basalt and hawaiite,in addition to mugearite,benmorite,and trachyte that occur mainly as domes,tuff cones and lava flows.Based on opaque mineralogy and mineral chemistry,the Harrat Rahat volcanic varieties are distinguished into Group I(olivine basalt and hawaiite) and Group II(mugearite,benmorite and trachyte).The maximum forsterite content(~85) is encountered in zoned forsteritic olivine of Group I,whereas olivine of Group II is characterized by intermediate(Fo=50),fayalitic(Fo=25) and pure fayalite in the mugearite,benmorite and trachyte,respectively.The more evolved varieties of Group II contain minerals that show enrichment of Fe2+,Mn2+and Na+that indicates normal fractional crystallization.The common occurrence of coarse apatite with titanomagnetite in the benmorite indicates that P5+becomes saturated in this rock variety and drops again in trachyte.Cr-spinel is recorded in Group I varieties only and the Cr#(0.5) suggests lherzolite as a possible restite of the Harrat Rahat volcanics.The plots of Cr# vs.the forsterite content(Fo) suggest two distinct trends,which are typical of mixing of two basaltic magmas of different sources and different degrees of partial melting.The bimodality of Harrat Rahat Cr-spinel suggests possible derivation from recycled MORB slab in the mantle as indicated by the presence of high-Al spinel.It is believed that the subcontinental lithospheric mantle was modified by pervious subduction process and played the leading role in the genesis of the Harrat Rahat intraplate volcanics.The trachytes of the Harrat Rahat volcanic field were formed most probably by melting of a lower crust at the mantle-crust boundary.The increase in fO2 causes a decrease in Cr2 O3,and Al2 O3,and a strong increase in the proportion of Fe3+and Mg# of spinel crystallizing from the basaltic melt at T ~1200°C.The olivine-pyroxene and olivine-spinel geothermometers yielded equilibrium temperature in the range of 935-1025°C,whereas the range of <500-850°C from single-pyroxene thermometry indicates either post crystallization reequilibrium of the clinopyroxene,or the mineral is xenocrystic and re-equilibrated in a cooling basaltic magma.     

Hydrothermal Mobilization and Enrichment of Iron in the Iron Deposits of the Middle—Lower Yangtze Valley District

There are two main types of iron deposits in the Middle-Lower Yangtze Valley district.Both of them underwent post-magmatic hydrothermal processes during ore formation.Iron in the hydrothermal ore bodies was derived largely through mobilization from substantially consolidated diroitic intrusives.Wall-roch alteration zonation indicates that iron-mobilizing hydrothermal fluids evolved in a trend of decreasing alkalinity,which is suggested by regularly distributed wall-rock alterations formed by iron-mobilizing hydrothermal fluids and is in contradiction with the current chloride,chloride complex and bicarbonate models for iron mobilization.The close association of carbonatization with iron ores and the high concentrations of reduced gases such as CO,CH4 and H2 in fluid inclusions suggest that iron is most probably transported in the form of iron carbonyls during post-magmatic hydrothermal processes. In the light of the iron carbonyl mobilization model,explanations are made of the constraints on ores of some geologic factors such as melanocratic alteration,carbonatization,carbonate strata,structural fractures,cyptoexplosive pipes and embryo ores.     

Characteristics and genesis of hematite in Chinese loess and paleosol sequences： Mineral genetic restriction for magnetic susceptibility as paleoclimate proxy and iron geochemistry

Hematite is an important iron oxide mineral in loess-paleosol sequences in central China. Investigation of the mineralogical characteristics, genetic mechanism and relationship of hematite with other iron oxides and Fe-bearing minerals will help understand the geochemical process before and after eolian deposit, paleocliamte significance of magnetic susceptibility and reconstruct paleoclimate in central China. So, hematite and related minerals of the loess and paleosol units from Chinese Loess Plateau were investigated using optical microscope, X-ray powder diffraction （XRD）, scanning electron microscopy （SEM）, and high-resolution transmission microscopy （HRTEM）. The results show that there are five genetic types of hematite in loess-paleosol sequences of central China： （1） weathering of Fe-bearing silicate minerals, for instance, chlorite, will release iron that is precipitated as aggregates of hematite nano-crystals on mineral surfaces; （2） hematite combined with eolian magnetite grains that resulted from partial oxidation of magnetite, even though the partial oxidation may occur in the original area; （3） phase transformation from eolian goethite to hematite; （4） hematite formed on the edge and surface of maghemite because of dissolution and hematite recrystallization; and （5） eolian detrial hematite. The hematite formed from chemical weathering of Fe-bearing silicates with nanoporous texture because of dehydration from iron hydroxide is the most important genetic mechanism. It is proposed that the fact that hematite was formed from chemical weathering of Fe-bearing silicates is a main reason for the redness in paleosol units. However, too intense pedogenesis and high amounts of precipitation will promote oxidation of eolian magnetite and maghemite dissolution, which may result in the decreasing of magnetic susceptibility.