最近13万年来黄土高原黄土剖面中绿泥石的化学风化与古气候变迁

对黄土高原不同纬度地区的4个黄土—古土壤剖面和lO个现代土壤样品中绿泥石的化学风化进行研究，发现黄土—古土壤剖面中的绿泥石在最近13万年发生了明显的化学风化，其风化程度受剖面位置和气候控制；黄土—古土壤剖面中ω(绿泥石 高岭石)／ω(伊利石)的比值与磁化率之间具有良好的负相关关系，绿泥石的化学风化与古土壤中铁氧化物矿物的形成和磁化率的增强之间有成因联系；黄土高原现代地表样品中ω(绿泥石 高岭石)／ω(伊利石)比值与现代年平均温度和年平均降水量有着良好的相关关系。认为ω(绿泥石 高岭石)／ω(伊利石)的比值可作为新的指示夏季风变化的替代性指标，对于定量重建古气候的变迁历史具有重要意义。     

Paleoclimate and Paleoenvironment of Gonghe Basin, Qinghai-Tibet Plateau, During the Lastdeglacial: Weathering, Erosion and Vegetation Cover Affect Clay Mineral Formation

With the analysis of the sources and formation mechanism of the clay minerals in the sediment core from the Dalianhai lake in the Gonghe Basin,northeastern Tibet-Qinghai Plateau,clay mineral composition proxies,grain-size and carbonate contents have been employed for high-resolution study in order to reconstruct East Asian Summer Monsoon （EASM） over the northeastern Tibet-Qinghai Plateau during the lastdeglacial.The study also extended to establish a relationship between vegetation cover changes and erosion during the last 14.5 ka with pollen record and clay mineral proxies.Smectite/kaolinite and smectite/（illite＋chlorite） ratios allow us to assess hydrolysis conditions in lowlands and/or physical erosion process in highlands of the Gonghe Basin.Before 12.9 Cal ka BP,both mineralogical ratios show low values indicative of strong physical erosion in the basin with a dominant cold and dry phase.After 12.9 Cal ka BP,an increase in both mineralogical ratios indicates enhanced chemical weathering in the basin associated with a warm and humid climate.The beginning of Holocene is characterized by high smectite/（illite＋chlorite） and smectite/kaolinite ratios that is synchronous as with deposition of many peat laminae,implying the best warm and humid conditions specifically between 8.0 to 5.5 Cal ka BP.The time interval after 5.0 Cai ka BP is characterized by a return to high physical erosion and low chemical weathering with dry climate conditions in the basin.Comparing variations of clay mineral assemblages with previous pollen results,we observe a rapid response in terms of chemical weathering and physical erosion intensity to a modification of the vegetation cover in the basin.     

Characterization of clay minerals in the Sundarban mangroves river sediments by SEM/EDS

Clay minerals, byproducts of chemical weathering, are important group of minerals found in rivers, estuaries, and marine sedimentary environments, which include mudstones, clay stones, and shales. In the present study, FTIR and SEM investigation on the clay minerals in Sundarban mangrove core sediments collected from Moipith Matla and Belamati Island are carried out. The study indicated the dominant association of kaolinite with subordinate amount of quartz, illite and chlorite. The abundance of kaolinite, illite chlorite and clay with quartz helps in increasing sediment in the islands region. The geochemical and mineralogical evolution of mangrove sediments are results of the interaction of biotic and abiotic parameters, whose balance is conditioned by the climate that governs the hydrologic regime, the sedimentation dynamics and the organic matter. This study on the charaterstation of clay provides us with substantial impact in the water holding capacity, productivity and mineralogical and chemical transformation in order to establish much more and intermediate equilibrium between marine influence and continental contribution, as part of the estuarine environment, than to the tropical climate conditions.     

上新世以来伊豆-小笠原海脊黏土矿物的来源与古气候意义

对伊豆-小笠原海脊(ODP 782A孔)上新世以来沉积物中黏土矿物的组成、含量及矿物学特征进行了分析,结果表明:黏土矿物以伊利石(42%)和蒙皂石(42%)为主,绿泥石的平均含量为14%,高岭石的含量最低,平均仅为2%。伊利石的结晶度较好,平均为0.25°Δ2θ;化学指数较低,平均为0.31;表明伊利石主要形成于干冷的气候环境。通过将ODP 782A孔黏土矿物组合特征和含量与周边可能源区对比,并结合伊利石和蒙皂石的矿物学参数特征,我们认为蒙皂石主要来源于伊豆-小笠原海脊周边岛弧火山物质;伊利石、绿泥石和高岭石主要来自亚洲大陆风尘。上新世以来(伊利石+绿泥石)/蒙皂石比值总体上呈增加的趋势,并且在5.3~3.6、3.6~1.6、1.6~0 Ma的三个阶段表现出不同的变化特征,该比值与全球深海δ¹⁸O值所记录的全球变冷、北太平洋ODP 885/886孔风尘通量和灵台黄土沉积速率,以及日本海U1430站伊利石/蒙皂石比值所指示的亚洲内陆干旱变化的总体变化趋势和阶段性变化的时间点大致同步,表明该比值敏感地响应了全球变冷和亚洲内陆的干旱。上新世以来(伊利石+绿泥石)/高岭石比值表现为高/低交替变化,分别与中国灵台黄土磁化率高/低变化相对应,由于黄土磁化率记录了亚洲内陆干/湿变化,因此该黏土矿物比值敏感地响应了亚洲内陆的古气候变化,因而可以作为可靠的亚洲大陆干/湿变化示踪指标。     

Clay Mineralogy and its Paleoclimatic Significance of the OligoceneMiocene Sediments in the Gerze Basin,Tibet

This study collected the early Oligocene to middle Miocene sediments from the Gerze Basin of Tibet, and used X-Ray diffraction （XRD） and Scanning Electron Microscope （SEM） to discuss their clay mineralolgy, clay indices, better understand the clay mineralogy and its paleoclimatic significance. The results show that clay minerals of the Gerze Basin sediments are mainly composed of iilite and chlorite, with minor amounts of smectite and kaolinite, and their relative content varies along the section. Variations of relative contents and clay indices suggest that the Gerze Basin has experienced three-stage evolution of paleoclimate： I ） high ilUte and chlorite contents, with fluctuant smectite and low （I＋Ch）/（K＋S） ratio, indicative of a dominant seasonal arid climate from the early Oligoeene to late Oligocene; Ⅱ） higher illite and chlorite contents and larger （I＋Ch）/（K＋S） ratio but absence of kaolinite, indicating a colder and drier climate from the late Oligocene to early Miocene; Ⅲ） high iilite and chlorite contents with fluctuant （I＋Ch）/（K＋S） ratios and occasional occurrence of kaolinite, suggesting that the climate became warmer and more humid compared with that of stage Ⅱ in the mid-Miocene. These conclusions were also reinforced by the clay morphology, which suggests that physical weathering dominated in stage Ⅱ, while relatively strong chemical weathering was dominant in stages Ⅰ and Ⅲ Clay minerals of the sediments mainly consist of illite and chlorite, indicating that the source rock played a significant role in clay origin. It is inferred that global cooling and the enhancement of denudation and obstruction of northward moisture due to the uplift of the Qinghai-Tibet Plateau were responsible for the provenance of iUite and chlorite under weak chemical weathering. Though the Qinghai-Tibet Plateau reached a certain elevation by the mid-Miocene, yet the mid-Miocene widespread warming might have largely impacted the Gerze climate.     

我国不同气候带黄土中粘土矿物组合特征分析

在兰州黄土和下蜀黄土中粘土矿物的X衍射分析基础上,对我国不同纬度和气候带的五个黄土剖面(点)中的粘土矿物组合和空间分布进行了对比分析,并探讨了与古气候的关系。结果表明,黄土中粘土矿物组合具有明显的地带性特征。从西北到东南,随着纬度的逐渐降低,黄土中的粘土矿物组合也发生有规律的变化。主要表现为绿泥石含量的逐渐减少和蛭石含量的逐渐增多。位于温带半干旱区的兰州黄土以伊利石和绿泥石为主要粘土矿物,而位于亚热带湿润区的大港下蜀黄土则以伊利石和蛭石为主要粘土矿物。黄土中含有较多量的绿泥石可作为黄土母质堆积后干冷气候和微弱风化的标志,而蛭石和蛭石/绿泥石混层矿物含量的增加指示了风化强度的增强。因此,黄土粘土矿物组合特征不仅反映物源区古环境信息,而且指示了黄土堆积期后的生物气候环境。     

Weathering processes affecting granitoid profiles of Capo Vaticano (Calabria,southern Italy) based on petrographic,mineralogic and reaction path modelling approaches

This work focuses on developing multidisciplinary research on weathering profiles of granitoid rocks related to the tectonic and landscape evolution of the Capo Vaticano area, Calabria, southern Italy. During the Pleistocene, the Mediterranean climate plays, on the already decomposed plutonic rocks, important processes of alteration, on both the highest and inland areas and the coastal areas of the Calabrian region, such as the studied area. Field observations coupled to chemical, minero‐petrographical features and geochemical modelling are used to characterize the weathering processes affecting the granitoid complex. The granitoid cut slopes show a generally simple weathering profile characterized by a progressive increase in weathering towards the top of the slopes. The completely weathered rocks (class V) and residual soil (class VI) contain a high percentage of altered minerals, microfractures, and voids. The main mineralogical changes are the partial transformation of biotite and the partial destruction of feldspars (mainly plagioclase) that are associated with the neoformation of secondary clay minerals and ferruginous products during the most advanced stage of weathering. These transformations produce a substitution of the original rock fabric. Geochemical modelling showing the precipitation of kaolinite, illite, vermiculite, ferrihydrite and calcite. These secondary solid phases are similar to those found in this natural system. Thus, the final results of the weathering process is a soil‐like material mainly characterized by mostly a sand to gravel grain‐size fractions related to microfabric changes and mineralogical and chemical variations. Copyright © 2014 John Wiley & Sons, Ltd.     

Preliminary studies on the characterization of clay minerals in the Sundarban mangrove core sediments,West Bengal,India

Clay mineral found in rivers, estuaries, and marine sedimentary environments is an important group of minerals which is the by-product of chemical weathering. The main constituents of this fine-grained sediment include mudstones, clay stones, and shales. This is probably the first report of a Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM) investigation on the clay minerals to characterize them in the Sundarban mangrove core sediments of Moipith Matla and Belamati Island. This study was carried out in the selected stretch for FTIR and SEM analyses. The study reveals the dominant association of kaolinite with subordinate amount of quartz, illite, and chlorite. The abundance of kaolinite, illite, chlorite, and clay with quartz helps in increasing the sediment in the island region. The geochemical and mineralogical evolution of mangrove sediment results in the interaction of biotic and abiotic parameters, whose balance is conditioned by the climate that governs the hydrologic regime, the sedimentation dynamics, and of the organic matter. This study on the characterization of clay provides substantial impact in the water-holding capacity, productivity, and mineralogical and chemical transformation in order to establish much more and intermediate equilibrium between marine influence and continental contribution, as a part of the estuarine environment.     

Weathering of the New Albany Shale, Kentucky, USA: I. Weathering zones defined by mineralogy and major-element composition

Comprehensive understanding of chemical and mineralogical changes induced by weathering is valuable information when considering the supply of nutrients and toxic elements from rocks. Here minerals that release and fix major elements during progressive weathering of a bed of Devonian New Albany Shale in eastern Kentucky are documented. Samples were collected from unweathered core (parent shale) and across an outcrop excavated into a hillside 40 year prior to sampling. Quantitative X-ray diffraction mineralogical data record progressive shale alteration across the outcrop. Mineral compositional changes reflect subtle alteration processes such as incongruent dissolution and cation exchange. Altered primary minerals include K-feldspars, plagioclase, calcite, pyrite, and chlorite. Secondary minerals include jarosite, gypsum, goethite, amorphous Fe(III) oxides and Fe(II)-Al sulfate salt (efflorescence). The mineralogy in weathered shale defines four weathered intervals on the outcrop—Zones A–C and soil. Alteration of the weakly weathered shale (Zone A) is attributed to the 40-a exposure of the shale. In this zone, pyrite oxidization produces acid that dissolves calcite and attacks chlorite, forming gypsum, jarosite, and minor efflorescent salt. The pre-excavation, active weathering front (Zone B) is where complete pyrite oxidation and alteration of feldspar and organic matter result in increased permeability. Acidic weathering solutions seep through the permeable shale and evaporate on the surface forming abundant efflorescent salt, jarosite and minor goethite. Intensely weathered shale (Zone C) is depleted in feldspars, chlorite, gypsum, jarosite and efflorescent salts, but has retained much of its primary quartz, illite and illite–smectite. Goethite and amorphous FE(III) oxides increase due to hydrolysis of jarosite. Enhanced permeability in this zone is due to a 14% loss of the original mass in parent shale. Denudation rates suggest that characteristics of Zone C were acquired over 1 Ma. Compositional differences between soil and Zone C are largely attributed to illuvial processes, formation of additional Fe(III) oxides and incorporation of modern organic matter.     

The nature and provenance of Golestan loess deposits in northeast Iran

Mineralogical, textural, geochemical, and weathering characteristics of loess deposits in Golestan province of Iran suggest that they are mostly derived from felsic igneous rocks and are related to Quaternary palaeoclimate. Whole‐rock analyses indicate heavy minerals such as zircon, tourmaline and phyllosillicate minerals (e.g. muscovite, chlorite, illite) exert a significant control on the chemical composition. The loess samples display uniform chemical composition, indicative of similar alteration history. Chemical index of alteration suggests a weak to moderate degree of weathering in a felsic source area. Scanning electron micrographs of quartz grains reveal abundant silt‐sized quartz particles, a result of glacial grinding during the Late Pleistocene in Central Asia. Subsequently, these silt particles were transported from Central Asia to their depositional site by wind and paraglacial processes. Local topography of northeast Iran (Alborz Mountains) acted as a major barrier, entrapping the airborne particles on the plains of Golestan province. Copyright © 2012 John Wiley & Sons, Ltd.     

南海北部中新世以来粘土矿物特征及东亚古季风记录

应用X射线衍射(XRD)、扫描电子显微镜(SEM) 和X射线能谱(EDS) 分析技术对南海北部ODP1146站中新世以来(~20 Ma) 粘土矿物的组成、结晶学特征、微形貌和化学成分进行了研究, 分析了粘土矿物的物质来源及其记录的东亚季风演化历史.1146站粘土矿物组合的总体特点是以伊利石和蒙脱石为主, 高岭石和绿泥石含量较低.物源分析表明, 1146站蒙脱石主要来自于吕宋岛, 伊利石和绿泥石来自于珠江和台湾(长江), 而高岭石则主要来自于珠江.1146站的粘土矿物不仅被南海周围物源的同时代气候所控制, 而且为相互消长的不同传输作用(表层洋流) 的强度所影响.1146站(伊利石+绿泥石) /蒙脱石比值可以用来作为东亚季风演化的矿物学标志.指标变化显示出东亚冬季风强度和冬季风相对夏季风的强度在15 Ma、8 Ma和3 Ma左右发生了3次显著加强, 结果可以与黄土、北太平洋风尘沉积、南海微体古生物记录等很好对比.青藏高原的阶段性隆升可能促进了东亚季风的这3次加强.      

Tschermak Substitution in Low- and Middle-grade Pelitic Schists

In low- and middle-grade pelitic metamorphic rocks, the extentsof Tschermak substitution in muscovite, chlorite and biotitechange regularly with bulk-rock composition and external conditions.This paper gives a theoretical analysis of the changes. From equipotential lines for Al₂O₃ plotted on AFM diagrams,we have derived a series of Thompson-type muscovite compositiondiagrams, which show how the celadonite content of muscovitevaries with the associated ferromagnesian minerals or with thebulk-rock composition under constant external conditions. Thedistribution coefficient of the exchange reaction for Tschermaksubstitution between muscovite and chlorite varies greatly notonly with temperature but also with the extent of this substitutionin the two minerals because of their strong deviation from ideality.Muscovites with a high celadonite content (phengites) occurin low-temperature rocks in any of the high-, medium- and low-pressuretypes of metamorphism, probably because the exchange equilibriumfor Tschermak substitution between muscovite and chlorite isnot sensitive to pressure. When both Mg-Fe and Tschermak substitutionoccur in muscovite and some other silicates, a metapelite containingthree AFM phases together with muscovite and quartz has at leasttwo independent net-transfer reactions that take place sideby side with changing external conditions. The mass balancerequirement in the rock is imposed on a linear combination ofthe two reaction equations, leading to a constraint on the stoichiometricequations among phase components and the progressive compositionalchanges of muscovite, chlorite and biotite. From such a viewpoint,we examine reactions and progressive mineralogical changes inmetapelites, beginning with K-feldspar-bearing low-grade metapeliticrocks, in which biotite appears by reaction of K-feldspar withchlorite at a temperature lower than that of the biotite isograddefined for K-feldspar-free pelitic rocks. When both Mg-Fe and Tschermak substitution occur in muscoviteand some other silicates, a metapelite containing three AFMphases together with muscovite and quartz has at least two independentnet-transfer reactions that take place side by side with changingexternal conditions. The mass balance requirement in the rockis imposed on a linear combination of the two reaction equations,leading to a constraint on the stoichiometric equations amongphase components and the progressive compositional changes ofmuscovite, chlorite and biotite. From such a viewpoint, we examinereactions and progressive mineralogical changes in metapelites,beginning with K-feldspar-bearing low-grade metapelitic rocks,in which biotite appears by reaction of K-feldspar with chloriteat a temperature lower than that of the biotite isoerad definedfor K-feldsoar-free oelitic rocks. The equations for the reactions that produce biotite or biotite? garnet in K-feldspar-free metapelites have been derived. Combinedwith the composition relations of coexisting muscovite, chlorite,biotite and garnet, they lead to the inference that progressof these reactions with rising temperature causes a decreaseof the celadonite content of muscovite, the antigorite contentof chlorite and the phlogopite content of biotite in the metapelitesof the chlorite, biotite and lower garnet zones, and that thistrend may not continue into the staurolite zone. This inferencehas been verified by examination of the analytical data of mineralsin four progressive metamorphic terranes covering the high-,medium- and low-pressure types. The composition of chlorite is buffered by the garnet-producingreaction so that chlorites in garnet-bearing metamorphic rocksdevelop (Mg ? Fe)/Al₂ ratios close to that of almandine at elevatedtemperatures. The maximum possible celadonite content in muscoviteunder given external conditions is realized in K-feldspar-bearingrocks, and decreases with rising temperature.     

Mineralogical changes during intense chemical weathering of sedimentary rocks in Bangladesh

Bangladesh is situated in a subtropical to tropical climatic zone. A recently weathered crust has developed on sedimentary bedrock (sandstone, siltstone, shale and claystones) of Tertiary–Quaternary age. Weathered samples were collected from 16 sections totaling 68 samples and were analyzed mineralogically. The main primary minerals identified in the weathered crust of sedimentary rocks are quartz, plagioclase, K-feldspar, biotite, muscovite, sparse carbonate and epidote. The secondary minerals are kaolinite, illite, chlorite, gibbsite and goethite. Weathering initiated along the grain boundaries and cleavage planes of the minerals, forming small cloudy materials which were very difficult to identify. In the advanced stage of weathering, these cloudy materials have turned into secondary minerals. In region 1, high rain fall (7100 mm/yr) and monsoonic climate resulted in a kaolinite–gibbsite–goethite suite through the weathering of feldspars and biotite. The occurrence of gibbsite in the relatively elevated lands of Sylhet and Fe-kaolinite throughout the study areas is indicative of a humid–tropical climate during formation of the weathered crust.     

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

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

Provenance of Clay Minerals in the Amami Sankaku Basin and Their Paleoclimate Implications Since Late Pleistocene

We analyzed the clay mineral assemblages, content and mineralogical characteristics of Hole U1438A sediment recovered from Amami Sankaku Basin during International Ocean Discovery Program (IODP) expedition 351. The results show that the clay minerals are mainly composed of illite (average 57%), smectite (average 26%), chlorite (average 14%) and minor kaolinite(average 3%). The crystallinity of illite in all samples are good (<0.4 Δ° 2θ), and the chemical indexes of illite in all samples are low (<0.4). Both indicate that illite in Hole U1438A formed in cold and dry climate. By comparing clay mineral assemblages of hole U1438A and the potential sediment sources, we suggest that smectite be mainly derived from the volcanic materials around Amami Sankaku Basin. Illite, chlorite and kaolinite are mainly derived from the Asian dust. The ratios of (illite+chlorite)/smectite show a phased increase over the last 350 ka, which is consistent with the cold and drying trend of the Asian continent since late Pleistocene. The high ratios of (illite+chlorite)/smectite and (illite+chlorite)/kaolinite during glacial period indicate that much more Asian dust was input into the Amami Sankaku Basin, which are responded to the aridity of Asian continent and strengthened east Asian Monsoon during glacial period.     

Formation of corrensite, chlorite and chlorite-mica stacks by replacement of detrital biotite in low-grade pelitic rocks

Transmission and scanning electron microscopy were utilized to investigate the nature and mechanisms of alteration of abundant detrital biotite of volcanic origin and progressive modification of phyllosilicate aggregates in a prograde sequence of pelitic rocks (illite crystallinity index = 0.19–0.58λ2θ) from the Gaspé Peninsula in Quebec.
Detrital biotite has been diagenetically altered to form corrensite and chlorite through two mechanisms; (1) layer-by-layer replacement gave rise to interstratification of packets of layers and complex mixed layering via several kinds of layer transitions between biotite and chlorite, corrensite or smectite; (2) dissolution-transport-precipitation resulted in the formation of relatively coarse-grained aggregates of randomly orientated, corrensite-rich flakes and fine-grained corrensite intergrown with chlorite and illite in the matrix.
The data show that stacks consisting of alternating packets of trioctahedral and dioctahedral phyllosilicates originated during early diagenesis when lenticular fissures in strained altering biotite were filled by dioctahedral clays. Subsequent prograde evolution of dioctahedral clays occurred through deformation, dissolution and crystallization, and overgrowth. Illite evolved to muscovite, with K in part provided through biotite alteration, and corrensite/chlorite to homogeneous chlorite. The alteration of detrital biotite is closely related to the formation of titanite and magnetite in diagenetic rocks, and pyrite, calcite and anatase or rutile in the higher grade rocks.
The observations demonstrate that detrital biotite of volcanic origin may be the principal precursor of chlorite in chlorite-rich metapelites originating in marginal basins. The mineral parageneses suggest that the transitions from corrensite to chlorite and illite to muscovite may be a function of local chemistry and time.     

Mineralogy and chemical composition of the clay fraction of Neogene shales from the Surma Group in the Bengal basin,Bangladesh

Mineralogical and chemical investigations (<2μm clay separates) of shale samples from the Neogene-age Surma Group obtained from four wells (Habiganj-11, Shahbazpur-1, Titas-11, Titas-15) in the Bengal basin, Bangladesh, were carried out in order to reveal the clay mineral composition as reservoir exploration and exploitation requires a good understanding of the clay minerals. The samples were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-Ray fluorescence spectrometry (XRF). Mineralogically, the sub-surface Surma Group shales comprise predominantly quartz, plagioclase, illite, chlorite, kaolinite, with lesser amounts of K-feldspar, dolomite and smectite, and minor to trace amounts of calcite, siderite and pyrite. The chemical composition of the <2 μm clay separates also suggests an illite and chlorite-rich composition. With increasing burial depth, the Surma Group shales are enriched in illite. The gradual decreasing of the smectite clays with depth and ultimate disappearance at greater depths (≥ 3000 m) may have been responsible for the presence of the diagenetic illite. Based on the mineralogical composition it is most likely that the illite-chlorite associations together with quartz and feldspar were predominantly detrital in origin and thus reflect the presence of a rapidly-rising source terrain not subjected to intense weathering.     

贵州碳酸盐岩红土中的粘土矿物及其形成机理

本文运用Ｘ射线衍射、红外光谱、差热、透射电镜和扫描电镜等方法对贵州碳酸盐岩红土中的粘土矿物进行了系统研究。高岭石和０．７ｎｍ埃洛石是碳酸盐岩红土中的主要粘土矿物，其次为伊利石、蛭石、绿泥石、绿泥石／蛭石混层矿物，水铝英石和三水铝石等。     

钱塘江下切河谷SE2孔全新世沉积物黏土矿物特征及其意义*

通过X射线衍射系统分析了杭州湾地区SE2孔全新世沉积物的黏土矿物组成,结果显示研究层段黏土矿物主要由伊利石、绿泥石、高岭石和蒙脱石组成;伊利石结晶度较好,化学风化指数普遍大于0.5,表明以化学风化为主,且风化趋势自下而上呈递减趋势。通过对比中国东南部主要河流沉积物的黏土矿物组成,认为钱塘江下切河谷全新世沉积物的黏土矿物组成具有较好的物源指示意义: 全新世 Ⅰ 段(即古河口湾和河漫滩)沉积物主要来自钱塘江上游,特征黏土矿物为高岭石,河口外物质贡献不大;Ⅱ 段(即现代河口湾和近岸浅海)沉积物包含较多蒙脱石,表明不仅包括钱塘江上游物质,河口外长江物质也开始进入钱塘江河口。黏土矿物中,高岭石对气候有较好的指示作用:中全新世高岭石含量达到最高值,反映气候最为湿热,化学风化程度最高;晚全新世含量逐渐降低,反映气候逐渐回冷,化学风化强度降低。     

Geochemical mass balance and weathering rates of ultramafic schists in Amazonia

The hydrochemical balance of the Yaou catchment in French Guiana was determined over a period of 1 year, combined with a detailed characterization of the primary minerals and their weathering products, in order to estimate ultramafic rock weathering rates in a rainforest environment. The time required to develop the main horizons of the laterite profile was obtained from estimations of the weathering rates and dissolution kinetics of some major parent minerals (chlorite, serpentine, biotite, calcite).

The specific transport of solute matter in the catchment is 205 kg/ha/a. The Cl and NO₃ net outputs shows that the system is in dynamic equilibrium, notably with respect to the biomass reservoir. The output flux of Mg in solution is mainly supplied from the weathering of primary minerals, whereas that of Ca comes both from atmospheric contributions and from the dissolution of carbonates. The fluxes of K and, more particularly, Na derive essentially from the atmosphere. Knowing the weathering rate of primary minerals, the total CO₂ consumption rate by silicate weathering is estimated at 1430 mol/ha/a.

The weathering rates of chlorite, serpentine and biotite range from 18 to 65 mol/ha/a, and those of talc and calcite are, respectively 51 and 153 mol/ha/a. Weathering rates normalized to mineral modal proportions give a decreasing order of stability resistance to weathering (calcitebiotitechlorite>serpentine>talc) that agrees with their vertical distribution in the weathering profile. The dissolution kinetics of chlorite, biotite and serpentine, expressed in relation to the Si release rate, were calculated using estimations of the mineral exchange surface by (a) optical microscope image processing of crystal outlines, and (b) BET specific surface measurements. The release rate of Si, computed for biotite, chlorite and serpentine, ranges around 10⁻¹³ and 10⁻¹⁴ mol/m²/s using microscope images on particle sizes. The estimated dissolution kinetics is two orders of magnitude lower when using the BET measured exchange surface, which is 100 times larger.

The saprolitization rate, calculated from the weathering rates of calcite, chlorite and biotite, is on average 7.5 m/Ma. The rate of latosol development, calculated from the weathering rate of serpentine at the saprolite–latosol interface, is estimated at 4.5 m/Ma. That means that the profile is chemically thickening at a rate of 3 m/Ma.