The Speeton Clay of North Yorkshire, England: An investigation of its geotechnical properties

The Lower Cretaceous in North Yorkshire is represented by a marine succession termed the Speeton Clay. The principal minerals in these clays consist of quartz, mica and clay minerals, although pyrite, glauconite and siderite are notable in some beds. The proportions of clay minerals change within the Speeton Clay and generally illite becomes more important in the younger horizons.

The Speeton Clay is a silty clay which generally has a high plasticity, the latter being influenced by the proportion of clay fraction present. All the clays tested were inactive although they would appear to have a potential for expansion. Neither the plasticity nor the moisture content were affected by depth.

In terms of its undrained shear strength, most of the Speeton Clay could be regarded as a stiff clay. It was also insensitive with generally a low slake-durability index. Its coefficients of volume compressibility were characteristic of overconsolidated and heavily overconsolidated days.     

Clay mineralogy, organic carbon burial, and redox evolution in Proterozoic oceans

Clay minerals formed through chemical weathering have long been implicated in the burial of organic matter (OM), but because diagenesis and metamorphism commonly obscure the signature of weathering-derived clays in Precambrian rocks, clay mineralogy and its role in OM burial through much of geologic time remains incompletely understood. Here we have analyzed the mineralogy, geochemistry and total organic carbon (TOC) of organic rich shales deposited in late Archean to early Cambrian sedimentary basins. Across all samples we have quantified the contribution of 1M and 1M_d illite polytypes, clay minerals formed by diagenetic transformation of smectite and/or kaolinite-rich weathering products. This mineralogical signal, together with corrected paleo-weathering indices, indicates that late Archean and Mesoproterozoic samples were moderately to intensely weathered. However, in late Neoproterozoic basins, 2M₁ illite/mica dominates clay mineralogy and paleo-weathering indices sharply decrease, consistent with an influx of chemically immature and relatively unweathered sediment. A late Neoproterozoic switch to micaceous clays is inconsistent with hypotheses for oxygen history that require an increased flux of weathering-derived clays (i.e., smectite or kaolinite) across the Precambrian-Cambrian boundary. Compared to previous studies, our XRD data display the same variation in Schultz Ratio across the late Neoproterozoic, but we show the cause to be micaceous clay and not pedogenic clay; paleo-weathering signals cannot be recovered from bulk mineralogy without this distinction. We find little evidence to support a link between these mineralogical variations and organic carbon in our samples and conclude that modal clay mineralogy cannot by itself explain an Ediacaran increase in atmospheric oxygen driven by enhanced OM burial.     

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.     

Environmental controls on clay mineralogy of an Early Jurassic mudrock (Blue Lias Formation,southern England)

We present a dataset including clay mineralogy, gamma-ray spectrometry, organic matter content and magnetic susceptibility of the Hettangian to lowest Sinemurian successions of Dorset and Somerset, southern UK (Blue Lias Formation, Bristol Channel and Wessex basins). In both areas, the clay assemblages comprise predominantly detrital illite, kaolinite and illite/smectite mixed layers. Clays probably originated from the erosion of the Hercynian massifs, the relative proportions of kaolinite and illite being modulated by arid-humid climatic fluctuations. The organic matter (OM) content (types II to IV) ranges up to 12% in both areas. A clear stratigraphical trend in clay mineral assemblages is apparent in Somerset, whereas in Dorset sharp contrasts between adjacent horizons and a greater dilution by carbonate mask the long-term evolution. Correlations between both areas based on similar vertical trends in clay mineral abundance support the suggestion of a hiatus within the angulata Zone of the Dorset succession. As expected, the kaolinite/illite ratio correlates with the Th/K ratio deduced from gamma-ray spectrometry. However, significant departures from the correlation occur in OM-rich intervals, suggesting that Th may be partly adsorbed on to OM particles. Surprisingly, high magnetic susceptibility correlates with abundant kaolinite, not with Fe-rich clays, indicating either that kaolinite is accompanied by a soil-inherited magnetisable phase (possibly iron oxide) or that illite-rich rocks are more strongly diluted by carbonate than are kaolinite-rich strata.     

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

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

The weathering of norite at Black Hill,South Australia

Black Hill is a boulder‐strewn residual of norite standing 45 m above the Murray Plains about 80 km northeast of Adelaide. Between the boulders, the crystalline rock has weathered to a dark‐brown terra rossa‐rendzina soil with calcite, illite, kaolin, and hematite as the principal secondary minerals. At one site on the smooth lower slopes of the outcrop, the material above the norite consists of partially weathered granular fragments with considerable dolomite and some calcite in nodular form. Below the surface, the rock has been weathered along joints to produce the clay mineral nontronite, and between each corestone and this plastic clay there is a zone of laminated but essentially unaltered rock 10–25 cm thick. Pieces of amorphous silica occur sporadically in some joints and on the surface.

The dark‐brown soil appears to be related to the present environment but the nontronite in the joint weathering, the dolomite, and the amorphous silica are all consistent with the norite having been inundated, possibly during the Miocene marine transgression.

Calculations based on the retention of elements such as aluminium, potassium, titanium, and iron have been used to predict quantitatively the amount of certain minerals such as quartz, calcite, and dolomite introduced to the weathering profiles.     

Geochemical and Mineralogical Characteristics of Pleistocene Lignites and Associated Sediments of Marathousa Coal Field,Central Peloponnese,Greece

The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite.     

滇黔北坳陷及邻区下志留统龙马溪组页岩气储层特征

基于8口钻井、2个剖面点的岩样观察和测试分析,滇黔北坳陷及邻区下志留统龙马溪组下段是富有机质泥页岩发育的层段,有机质演化达到过成熟阶段。X衍射全岩分析表明,龙马溪组泥页岩由黏土矿物、石英、碳酸盐、长石、黄铁矿等矿物组成,黏土矿物则以伊利石为主。泥页岩的平均脆性指数56.11%~73.21%,压裂时易于形成网络裂缝;常规物性测试,孔隙度、渗透率很低,扫描电镜观察,纳米级孔隙和裂缝发育。     

Effects of weathering on organic matter: Part II: Fossil wood weathering and implications for organic geochemical and petrographic studies

Bulk geochemical, petrographical, mineralogical and molecular compositions of unweathered, weathered and transitional zones of a Middle Jurassic fossil wood were analyzed to trace changes caused by oxidative weathering of the immature terrestrial organic matter (OM). The occurrence of such zones was confirmed by the mineral composition, showing replacement of siderite and pyrite by goethite. Vitrinite reflectance analysis of weathered and unweathered fossil wood samples revealed that weathering elevated the vitrinite reflectance values by ca. 0.1%, which should be taken into account during modeling of low maturity terrestrial OM. In the weathered part of the wood, most of the biomarkers and biomolecules were totally removed or the concentration decreased significantly. The concentration of most of the polynuclear aromatic hydrocarbons (PAHs) decreased by 50–80%, being >90% for the more reactive and less stable benzo[a]pyrene and perylene. On the other hand, several aromatic compounds, like phenanthrene and its methyl derivatives, phenyl naphthalenes, fluoranthene and oxygen-containing aromatic compounds increased in concentration in the weathered zone. This results from processes such as formation of phenyl derivatives of PAHs and their cyclization, as well as aromatization of diterpenoids and incorporation of oxygen into aromatic structures. Weathering should always be considered in studies of fossilized terrestrial OM, especially in the case of thermal maturation modeling, because it significantly decreases the OM content and total sulfur content, changes vitrinite reflectance values and alters the extract composition as a result of organic compound degradation.     

Septarian concretions from the Oxford Clay (Jurassic, England, UK): involvement of original marine and multiple external pore fluids

Septarian concretions occur at several horizons within the Oxford Clay Formation, a marine mudstone containing pristine aragonite and immature biomarker molecules. They record the passage of at least four generations of pore fluids, the first of marine origin and the last still present in cavities. Concretion bodies formed, cracked, and calcite and pyrite precipitated in and around the cracks within the sulphate reduction zone, as demonstrated by C, O, S and Sr isotopic composition (Pore fluid 1). Before major compaction, sandstone dykes were intruded locally, and baryte precipitated, followed by coarse calcite cements with isotopically light oxygen and radiogenic strontium, indicating the introduction of meteoric-derived water (Pore fluid 2). Later, coarse celestine within concretions has distinct sulphur-isotopic composition and requires a further, geographically restricted, water source (Pore fluid 3). Celestine-bearing concretions contain water in tight cavities whose isotopic composition is close to that of modern precipitation. Its chemistry shows that it is equilibrating with pre-existing minerals implying a relatively recent origin (Pore fluid 4). The mineralogy of the Oxford Clay concretions shows that complex results can follow from a simple burial and uplift history, and that multiple generations of pore fluids can pass through a low-permeability clay.     

Sub‐Cambrian pedogenesis recorded in weathering profiles of the Arabian‐Nubian Shield

Altered crystalline rocks occur at the peneplain exposed in southern Israel and in other localities across North Africa and Arabia where they underlie an extensive blanket of Cambro–Ordovician sandstones. This study focuses on the petrography, mineralogy and geochemistry of top basement rocks of the northern Arabian‐Nubian Shield. The altered rocks are shown to be weathering profiles that can be subdivided into three horizons interpreted as apparently unweathered granite, or saprock, which grades upwards to a saprolite, topped by a thin clayey plasmic zone. The plasmic zone is enriched in iron and aluminium and is depleted in silicon, calcium, magnesium and potassium relative to the underlying saprolite. The chemical index of alteration increases upward, but does not exceed 90 and, therefore, lags behind values observed in strongly leached present‐day tropical soils. Petrographic examinations reveal iron mobility under local fluctuating redox conditions, similar to modern and Proterozoic soils. A variety of birefringence fabrics induced by shrinkage and expansion of clays during wetting and drying cycles and clay illuviation strongly indicate pedogenic processes rather than a post‐depositional alteration. Illite and ordered illite‐smectite phases coexist with smectitic illite‐smectite in the lower part of the saprolite and with kaolinite in the plasmic zone, in line with increasing chemical index of alteration. Observations are in accordance with the current profile being a remnant of a thick weathering profile whose top was truncated by fluvial incision just prior to deposition of the overlying Early Cambrian sequence. A previously documented Devonian thermal event reaching temperatures of at least 200°C overprinted the studied rocks. During burial diagenesis, illitization affected original smectite rather than kaolinite. However, in spite of the elevated temperatures, illitization was incomplete implying restricted potassium addition. The sub‐Cambrian weathering reflects warm and humid conditions in a tropical or sub‐tropical climate, in line with several plate reconstructions placing Israel at low latitudes during Cambrian time.     

Palygorskite from cave sediments: case study from Wadi Haqil,United Arab Emirates

The x-ray powder diffraction identification of clay minerals both in bulk samples and in separated clay fraction confirmed the presence of palygorskite in samples of cave sediments from Wadi Haqil (the western slopes of Musandam Mountains; Ras Al-Khaimah Emirate, UAE). Samples contain quartz, gypsum, smectite, kaolinite, calcite, and palygorskite, some of them chlorite, illite, feldspars, and goethite. Calcite dominates in most samples; smectite prevails in clay fraction. After heating, the 001 reflection of chlorite shifts to higher diffraction angles and its intensity decreases; these features indicate that the chlorite represent a Fe-dominant species. Unit-cell dimensions of major phases as refined by the Rietveld method are in agreement with literature data. Chemical composition of palygorskite was derived from unit-cell dimensions as follows: MgO content is 11–14 wt% and Al₂O₃ 10–13 wt%. Clay mineralogy is only hard to ascertain from the scanning electron microscope (SEM) images even after being combined with the energy-dispersive spectrometer data. The SEM was also used to characterize gypsum grains; they often display flow deformation features. Studied cave sediments represent palygorskite-bearing weathering products and desert soils re-deposited from the cave surroundings by slope processes and wind and/or surface runoff. The mixture with other clay minerals, quartz, feldspars, etc. supports this interpretation. Fine-grained quartz fraction is probably wind-blown. Gypsum and calcite are the precipitates (crusts and/or cements), although gypsum can also be re-deposited from omnipresent gypsum-cemented surface sediments.     

Climatic control on clay mineral formation: Evidence from weathering profiles developed on either side of the Western Ghats

Many physico-chemical variables like rock-type, climate, topography and exposure age affect weathering environments. In the present study, an attempt is made to understand how the nature of clay minerals formed due to weathering differs in tropical regions receiving high and low rainfall. Clay mineralogy of weathering profiles in west coast of India, which receives about 3 m rainfall through two monsoons and those from the inland rain-shadow zones (<200 cm rainfall) are studied using X-ray diffraction technique. In the west coast, 1:1 clays (kaolinite) and Fe—Al oxides (gibbsite/goethite) are dominant clay minerals in the weathering profiles while 2:1 clay minerals are absent or found only in trace amounts. Weathering profiles in the rain shadow region have more complex clay mineralogy and are dominated by 2:1 clays and kaolinite. Fe—Al oxides are either less or absent in clay fraction. The kaolinite—smectite interstratified mineral in Banasandra profiles are formed due to transformation of smectites to kaolinite, which is indicative of a humid paleoclimate. In tropical regions receiving high rainfall the clay mineral assemblage remains the same irrespective of the parent rock type. Rainfall and availability of water apart from temperature, are the most important factors that determine kinetics of chemical weathering. Mineral alteration reactions proceed through different pathways in water rich and water poor environments.     

Clay mineralogy of archaeological soil: an approach to paleoclimatic and environmental reconstruction of the archaeological sites of the Paharpur area,Badalgacchi upazila,Naogaon district,Bangladesh

A geo-archaeological examination was carried out in and around the Paharpur area, Badalgacchi upazila of Naogaon District in the north-western part of Bangladesh. Clay mineralogy and global paleo-temperature curves were used to determine the paleoclimatic and depositional environmental conditions of the Holocene archaeological soils (Barind clay residuum) of the Paharpur archaeological spot. Clay mineralogical data show that the dominant clay mineral is illite with subordinate amounts of kaolinite and chlorite. The high illite and low kaolinite content implies a marine or estuarine deposit. The clay mineral ratio log diagram, constructed by plotting the 7–10°Å integrated intensity ratios versus depth, supports this assumption. The presence of illite, together with quartz and feldspar, suggests high detrital input under generally cool to temperate and dry climates. Chlorite is another common by-product of weathering reactions with low hydrolysis, which is typical for cool to temperate and dry climates. The results suggest the existence of a marine–estuarine influence under a generally cool to temperate and dry climates around Paharpur and the surrounding region throughout the Pala dynasty around mid-century 700 a.d. to early 1100 a.d. Furthermore, this observation is consistent with the global paleo-temperature curves.     

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.     

Chemical weathering in Luzon, Philippines from clay mineralogy and major-element geochemistry of river sediments

Clay mineralogy and major-element geochemistry of 35 surface sediment samples collected in 21 major to moderate rivers of Luzon, Philippines are used to evaluate the present chemical weathering process. The clay mineral assemblage consists mainly of smectite (average 86%) with minor kaolinite (9%) and chlorite (5%) and very scarce illite (1%), and does not show strong island-wide differences. The major element results of both bulk and clay-fraction sediments indicate that the formation of clay minerals is accompanied by leaching of Ca and Na first and of Fe and Mn thereafter during the chemical weathering process. A low-moderate chemical weathering degree of bulk sediments and a moderate-intensive degree of clay-fraction sediments are obtained in Luzon rivers based on proxies of chemical index of alteration (CIA) and smectite crystallinity. It is suggested that the majority of andesitic–basaltic volcanic and sedimentary rocks along with the tectonically active geological setting and sub-tropical East Asian monsoon climate are responsible for the predominance of smectite in the clay mineral assemblage.     

Weathering of the New Albany Shale, Kentucky: II. Redistribution of minor and trace elements

During weathering, elements enriched in black shale are dispersed in the environment by aqueous and mechanical transport. Here a unique evaluation of the differential release, transport, and fate of Fe and 15 trace elements during progressive weathering of the Devonian New Albany Shale in Kentucky is presented. Results of chemical analyses along a weathering profile (unweathered through progressively weathered shale to soil) describe the chemically distinct pathways of the trace elements and the rate that elements are transferred into the broader, local environment. Trace elements enriched in the unweathered shale are in massive or framboidal pyrite, minor sphalerite, CuS and NiS phases, organic matter and clay minerals. These phases are subject to varying degrees and rates of alteration along the profile. Cadmium, Co, Mn, Ni, and Zn are removed from weathered shale during sulfide-mineral oxidation and transported primarily in aqueous solution. The aqueous fluxes for these trace elements range from 0.1 g/ha/a (Cd) to 44 g/ha/a (Mn). When hydrologic and climatic conditions are favorable, solutions seep to surface exposures, evaporate, and form Fe-sulfate efflorescent salts rich in these elements. Elements that remain dissolved in the low pH (<4) streams and groundwater draining New Albany Shale watersheds become fixed by reactions that increase pH. Neutralization of the weathering solution in local streams results in elements being adsorbed and precipitated onto sediment surfaces, resulting in trace element anomalies.Other elements are strongly adsorbed or structurally bound to solid phases during weathering. Copper and U initially are concentrated in weathering solutions, but become fixed to modern plant litter in soil formed on New Albany Shale. Molybdenum, Pb, Sb, and Se are released from sulfide minerals and organic matter by oxidation and accumulate in Fe-oxyhydroxide clay coatings that concentrate in surface soil during illuviation. Chromium, Ti, and V are strongly correlated with clay abundance and considered to be in the structure of illitic clay. Illite undergoes minimal alteration during weathering and is concentrated during illuvial processes. Arsenic concentration increases across the weathering profile and is associated with the succession of secondary Fe(III) minerals that form with progressive weathering. Detrital fluxes of particle-bound trace elements range from 0.1 g/ha/a (Sb) to 8 g/ha/a (Mo). Although many of the elements are concentrated in the stream sediments, changes in pH and redox conditions along the sediment transport path could facilitate their release for aqueous transport.     

兰州盆地永登剖面晚古新世—早渐新世沉积物中粘土矿物的特征及其古气候指示意义

采用X射线衍射、扫描电镜分析方法,对兰州盆地永登剖面晚古新世—早渐新世沉积物中粘土矿物的相对含量、伊利石结晶度、显微形貌及其古气候意义进行深入研究。结果表明:晚古新世—早渐新世沉积物中粘土矿物主要为伊利石、蒙脱石、绿泥石和少量的坡缕石,其中伊利石的含量最高,而且从晚古新世到早渐新世,沉积物中伊利石的含量呈明显升高的趋势,蒙脱石则呈明显减少的趋势;在大约55 Ma处伊利石含量急剧减小,而蒙脱石含量急剧增大。此外,可见到毛发状的自生坡缕石沿蒙脱石晶片边缘交代生长,而碎屑成因的坡缕石则主要呈破碎的短棒状。粘土矿物分布特征表明,兰州盆地晚古新世—早渐新世的古气候以干旱为主导,并且经历了由相对温暖湿润到半干旱半湿润或干旱炎热的转变,这种气候转型主要受全球气候的影响,即受行星风系的控制;而在大约55 Ma处伊利石、蒙脱石的含量变化则记录了全球性的PETM事件。     

Provenance of iron,bauxite and clay deposits of the Carboniferous Benxi Formation in southern margin of North China Craton: An example from Da'an bauxite and clay deposit of Sanmenxia area,Henan Province

During the Middle Ordovician to Late Carboniferous period,the North China Craton(NCC)was exposed and experienced prolonged weathering that resulted in the formation of large-scale iron,clay and bauxite deposits. The source of ore-forming material has always been a research focus,in particular,whether the sources of the iron ore and the Fe-bearing clay at the bottom of Benxi Formation are the same as the upper bauxite and clay deposit is still unclear. In this study,the Da'an bauxite and clay deposit at the southern margin of the NCC was chosen to carry out a detailed analysis of the micro-region mineral composition and elemental geochemical characteristics for further exploring the sources of iron,bauxite and clay deposits. The composition of the ore-bearing rocks in the Da'an bauxite deposit from the bottom to top includes Fe-bearing clay(locally iron ore),bauxite,and bauxitic clay;locally,in karstic uplift,bauxitic clay layer is directly overlying on the Fe-bearing clay. The Fe-bearing clay is dominated by siderite,pyrite,and illite in the karstic depression,and hematite,illite,and kaolinite in the uplift. Bauxite is mainly composed of diaspore,illite,and anatase,while bauxitic clay is mainly composed of illite. Mineral microanalysis revealed the development of large amounts of moissanite and small amounts of natural silica,silicalite,and chromite at the bottom of bauxitic clay layer. Regional comparison and correlation reveal that the ophiolite in the Shangdan suture zone and Erlangping Group in the North Qinling orogenic belt(NQOB)likely provides source materials for bauxite and clay deposits. The obvious differences in immobile element ratios (e.g., Zr/TiO₂,Hf/TiO₂,Nb/TiO₂,Ta/TiO₂)between the bottom Fe-bearing clay layer and the upper bauxite and clay layer in Da'an deposit,revealing that they are from different sources. The bottom Fe-bearing clay and iron ore layers are the products of in-situ weathering of underlying carbonates,while the top bauxite and clay are allochthonous. The regional uplift of the NQOB during the Late Carboniferous period provided important ore-forming materials for the formation of the NCC bauxite and clay deposits.     

华北克拉通南缘石炭系本溪组铁-铝黏土矿物质来源: 以河南三门峡大安铝黏土矿床为例*

华北克拉通在中奥陶世至晚石炭世期间一直出露地表,经历了长期的风化作用,形成大规模的铁-铝黏土矿,其成矿物源一直是研究的热点,尤其是本溪组底部铁矿和铁质黏土矿与上部铝黏土矿是否为同一来源尚未查清。本研究选取克拉通南缘大安铝黏土矿床作为研究对象,展开微区矿物及元素地球化学组成分析,进一步探讨铁-铝黏土矿物质来源。大安矿床内含矿岩系自下而上包括铁质黏土岩、铝土矿、铝质黏土矿;局部喀斯特高地缺失铝土矿,铝质黏土矿直接覆盖于铁质黏土岩之上。铁质黏土岩在洼地以菱铁矿、黄铁矿和伊利石为主,在隆起区以赤铁矿、伊利石和高岭石为主。铝土矿以硬水铝石、伊利石和锐钛矿为主;铝质黏土矿主要矿物为伊利石。矿物微区分析在黏土矿底部发现大量的碳化硅和少量自然硅、硅铁矿、铬铁矿;区域对比揭示北秦岭造山带内商丹缝合带和二郎坪群中的蛇绿岩为铝黏土矿形成提供了成矿物质。本溪组底部铁质黏土与上部铝黏土矿稳定元素比率(例如Zr/TiO₂、Hf/TiO₂、Nb/TiO₂、Ta/TiO₂)存在明显差异,揭示二者为不同来源: 底部铁质黏土岩和铁矿层为底板碳酸盐岩原地风化的产物;而上部铝黏土矿是异地搬运物,北秦岭造山带在晚石炭世的整体抬升为华北铝黏土矿形成提供了重要的成矿物质。