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1.
《Journal of Asian Earth Sciences》2006,26(6):893-902
Pedogenic calcretes commonly exhibit clotted micrite, circum-granular calcite (grain coats) and microspar/spar veins. The three calcite-types with different dimensions were analyzed for their magnesium content to determine the relationship between crystal elongation and magnesium incorporation. The results show a very low MgO content for grain coats and microspars and high values for clotted micrite indicating that the ideal kinetic model does not hold true and several variables govern the end composition of calcites. The magnesium concentrations of meteoric calcites are genetically linked to the evolutionary history of the soil and climate. Grain coats, which are elongated calcites, contain the least amount of Mg and is related to the initial stages of pedogenesis wherein the limiting factor is the Mg/Ca ratio of the parent fluid. Lower magnesium contents arise due to smaller quantities of Mg being released during incipient weathering. Micrite morphology and composition is controlled by the greater availability of Mg ions through weathering, higher pCO2 in soil due to increased time-dependent soil respiration, which causes a rise in calcite precipitation rates and clay authigenesis. This in turn exerts a physical control on morphology by occluding pore space and providing numerous nuclei for calcite precipitation. The wide variability in spar cements is inherently controlled by inhomogeneties in parent fluid compositions with lower-than-micrite values on account of slower precipitation rates. 相似文献
2.
Elemental composition of calcites in late Quaternary pedogenic calcretes from Gujarat, western India
Aniruddha S. Khadkikar 《Journal of Asian Earth Sciences》2005,25(6):893-902
Pedogenic calcretes commonly exhibit clotted micrite, circum-granular calcite (grain coats) and microspar/spar veins. The three calcite-types with different dimensions were analyzed for their magnesium content to determine the relationship between crystal elongation and magnesium incorporation. The results show a very low MgO content for grain coats and microspars and high values for clotted micrite indicating that the ideal kinetic model does not hold true and several variables govern the end composition of calcites. The magnesium concentrations of meteoric calcites are genetically linked to the evolutionary history of the soil and climate. Grain coats, which are elongated calcites, contain the least amount of Mg and is related to the initial stages of pedogenesis wherein the limiting factor is the Mg/Ca ratio of the parent fluid. Lower magnesium contents arise due to smaller quantities of Mg being released during incipient weathering. Micrite morphology and composition is controlled by the greater availability of Mg ions through weathering, higher pCO2 in soil due to increased time-dependent soil respiration, which causes a rise in calcite precipitation rates and clay authigenesis. This in turn exerts a physical control on morphology by occluding pore space and providing numerous nuclei for calcite precipitation. The wide variability in spar cements is inherently controlled by inhomogeneties in parent fluid compositions with lower-than-micrite values on account of slower precipitation rates. 相似文献
3.
苏皖玄武岩土壤中风尘的识别及风化特征 总被引：1，自引：0，他引：1
风尘传输与沉降影响生态系统和元素的生物地球化学循环,对其在成壤作用中的识别与贡献进行研究有重要意义。文章选择在非风尘沉降区的苏皖玄武岩台地典型的两个风化剖面（安徽明光梅花村和江苏盱眙宝塔村）和部分表土及水系沉积物样品,系统分析主要矿物、粘土矿物、常量元素、微量元素及Sr、Nd同位素组成。结果显示,玄武岩基岩基本由斜长石和辉石组成,而风化基岩则主要由蒙脱石构成,风化土壤则出现基岩和风化基岩中未出现的石英、伊利石等风尘特征矿物;基岩和风化基岩以高Mg,低Si、K,无Eu异常等特征,风化土壤则以高Si、K,低Mg,负Eu异常等特征;基岩和风化基岩的εNd偏正,86Sr/87Sr值较低,而风化土壤εNd偏负,86Sr/87Sr值较高;各种证据都显示风尘对风化土壤有重要贡献,通过Nd同位素混合模式计算,风尘对土壤的贡献达60%以上。玄武岩风化表现为完全的蒙脱石化,为显著的去Ca、Mg作用,在梅花村剖面,表层土壤出现Ce负异常,而在下部层位出现Ce正异常,研究还发现在风尘的加积作用,土壤的Si、K含量得以上升。受相对较大的玄武岩台地高程差影响,玄武岩风化产物和沉降的风尘易被降水侵蚀,造成风化剖面较薄,促使玄武岩风化处于“供应限制”模式。本次工作为玄武岩的风化机制,风尘在元素地球化学循环中的作用等提供了新的地质证据。 相似文献
4.
Prediction of some weathering trends of plutonic and volcanic rocks based on thermodynamic and kinetic considerations 总被引：18，自引：0，他引：18
The exposed crust consists mainly of plagioclase (35%), quartz (20%), K-feldspar (11%), volcanic glass (12%), biotite (8%), and muscovite (5%). Quartz is a resistate, thus feldspars and glass represent approximately 75 percent of the labile minerals. The weathering characteristics of these constituents are summarized in the context of thermodynamic, mass balance and kinetic considerations.Experimentally determined release rate constants were used to predict the proportions of Ca, Na and K released by feldspars of plutonic rocks (granites to gabbros) to weathering solutions. The chemical weathering trends of the weathered residues, calculated from the kinetic data, conform closely to the initial trends observed in some recent weathering profiles, demonstrating the accuracy of the predictions. Since the weathering of feldspars is controlled by processes that should not change through geological time, the relative release rates of Ca, Na, and K from the feldspars of granitic rocks can be calculated for future and past episodes of continental weathering.Experimentally determined release rate constants are not available for a wide range of volcanic glass compositions, but the limited data indicate that compositional trends are predictable in weathering profiles developed on volcanic rocks. The kinetic data available for rhyolitic glasses accurately predict the initial weathering trends observed in a recent rhyolite weathering profile. 相似文献
5.
黑色页岩是富含有机质和硫化矿物的特殊沉积岩,但人们对其风化过程的元素活动性及矿物风化机制关注较少.为探讨不同地形位置的黑色页岩化学风化过程,采集了渝东北城口某山脊 (A)、近山顶 (B) 和沟谷 (C) 的下寒武统水井沱组黑色页岩风化剖面岩样,利用XRD、XRF和化学分析手段对采集样品的矿物成分、主量元素进行测定分析.元素和矿物的质量迁移系数 (τ) 和质量迁移通量 (Mj, flux) 的计算结果表明,黑色页岩风化过程中Ca、Mg和Na元素具有明显的贫化现象,近地表处存在Al元素的富集现象;矿物成分方面,黄铁矿和有机质氧化后形成的酸性水环境,造成方解石、白云石、斜长石等不稳定矿物溶解,并生成含水石膏、铁质氧化物、黏土矿物等次生矿物.不同赋存位置的黑色页岩风化程度有所差异,Na/K-CIA、K/Ca*-Al/Na、A-CN-K和A-CNK-FM图解显示:A剖面处于脱Ca过程的初级风化阶段,B剖面处于脱Ca、Na初期的初等-中等风化阶段,C剖面已发生脱Ca、Na过程,并伴随脱Si作用的中等-强烈风化阶段,结合不同风化指数 (如:CIA、CIW、PIA、MWPI等),得出各剖面的化学风化强弱程度依次为C＞B＞A. 相似文献
6.
《Applied Geochemistry》2006,21(2):352-376
Chemical weathering rates for a mudstone obtained from a mining environment were investigated using a combination of batch reactors and hydrologically unsaturated column experiments. Results of tracer tests were combined with relationships between solute concentrations, mass fluxes, flow rates and residence times, and used to calculate element release rates and infer rate-controlling mechanisms for the two different experimental environments.Elements that eluted from column experiments exhibited either:
- (1)concentrations independent of flow rate and column length coupled with mass flux increasing with flow rate, or
- (2)an inverse relationship between concentration and flow rate coupled with mass flux increasing with both column length and flow rate.
7.
地壳风化速率研究综述 总被引：6，自引：1，他引：6
地壳风化速率研究的理论基础是质量守恒原理和溶液与矿物反应动力学法则。元素在风化过程中的行为受多种因素控制，主要包括基岩风化量、大气沉降量、径流量、生物的输出数量和人为输入量（如施肥）。硅酸盐矿物化学风化过程中，矿物与溶液之间总的化学反应速率是单个反应速率之和，其中涉及到 3个关键参数，即：酸中和能力（ANC）、基本阳离子/无机铝（BC/Al无机）比值和临界负荷（CL）。风化速率的研究主要采用四种方法，即PROFILE模型、基本阳离子损耗、元素输入-输出指数和Sr同位素比值等。PROFILE模型是一个稳定态的综合土壤化学模型，矿物的分解速率、矿物的暴露表面积、土壤水饱和度和土壤层厚度决定着该矿物的风化速率，总的风化速率为各种矿物的风化速率之和。元素损耗，主要是基本阳离子（Ca、Na、K和Mg）的损耗，假设Ti、 Zr和Nb在成土过程中含量稳定并不参与风化反应，那么对于给定的土壤层，化学风化损耗的基本阳离子可以通过比较土层与成土母质之间元素组成的差异来计算。输入-输出指数的假设前提是研究的流域处于稳定状态，一般认为输入指数是大气沉降，输出指数是河流搬运溶解部分、悬浮的非岩屑成因部分和生物营养净吸收部分。Sr同位素在生物和化学作用过程中并不分馏，不同生态系统阳离子场中Sr同位素组成是大气和矿物风化来源的Sr的混合物。 相似文献
8.
《Applied Geochemistry》1999,14(3):387-394
Mineral weathering rates for two chronosequences of soils have been calculated using an empirical method based on mineralogy, the depletion of elements relative to a conservative element and the computer model PROFILE. Weathering rates calculated by the empirical and depletion methods showed a decrease in rates with soil age whilst those calculated using the PROFILE model showed an increase with soil age. The counter intuitive PROFILE prediction is due to the use of surface area—normalised reaction rate coefficients which assume that: 1) mineral reactivity is constant with time and, 2) total mineral surface area is equivalent to reactive surface area.In Europe, mineral weathering rates in soils are an important input in determining levels of acid deposition above which ecosystem damage will occur (critical loads). As soils in Great Britain and much of NW Europe can range in age from <103 to >105 a, it is suggested that, until computer models can take account of soil age and the concomitant changes in mineral reactivity and surface area, modelled weathering rates will be subject to large uncertainties 相似文献
9.
Christopher Oze Catherine Skinner Andrew W. Schroth Robert G. Coleman 《Applied Geochemistry》2008,23(12):3391-3403
Serpentine soils derived from the weathering of ultramafic rocks and their metamorphic derivatives (serpentinites) are chemically prohibitive for vegetative growth. Evaluating how serpentine vegetation is able to persist under these chemical conditions is difficult to ascertain due to the numerous factors (climate, relief, time, water availability, etc.) controlling and affecting plant growth. Here, the uptake, incorporation, and distribution of a wide variety of elements into the biomass of serpentine vegetation has been investigated relative to vegetation growing on an adjacent chert-derived soil. Soil pH, electrical conductivity, organic C, total N, soil extractable elements, total soil elemental compositions and plant digestions in conjunction with spider diagrams are utilized to determine the chemical relationships of these soil and plant systems. Plant available Mg and Ca in serpentine soils exceed values assessed in chert soils. Magnesium is nearly 3 times more abundant than Ca in the serpentine soils; however, the serpentine soils are not Ca deficient with Ca concentrations as high as 2235 mg kg−1. Calcium to Mg ratios (Ca:Mg) in both serpentine and chert vegetation are greater than one in both below and above ground tissues. Soil and plant chemistry analyses support that Ca is not a limiting factor for plant growth and that serpentine vegetation is actively moderating Mg uptake as well as tolerating elevated concentrations of bioavailable Mg. Additionally, results demonstrate that serpentine vegetation suppresses the uptake of Fe, Cr, Ni, Mn and Co into its biomass. The suppressed uptake of these metals mainly occurs in the plants’ roots as evident by the comparatively lower metal concentrations present in above ground tissues (twigs, leaves and shoots). This research supports earlier studies that have suggested that ion uptake discrimination and ion suppression in the roots are major mechanisms for serpentine vegetation to tolerate the chemistry of serpentine soils. 相似文献
10.
K. Srinivasamoorthy S. Chidambaram M. V. Prasanna M. Vasanthavihar John Peter P. Anandhan 《Journal of Earth System Science》2008,117(1):49-58
The study area Mettur forms an important industrial town situated NW of Salem district. The geology of the area is mainly
composed of Archean crystalline metamorphic complexes. To identify the major process activated for controlling the groundwater
chemistry an attempt has been made by collecting a total of 46 groundwater samples for two different seasons, viz., pre-monsoon
and post-monsoon. The groundwater chemistry is dominated by silicate weathering and (Na + Mg) and (Cl + SO4) accounts of about 90% of cations and anions. The contribution of (Ca + Mg) and (Na + K) to total cations and HCO3 indicates the domination of silicate weathering as major sources for cations. The plot for Na to Cl indicates higher Cl in
both seasons, derived from Anthropogenic (human) sources from fertilizer, road salt, human and animal waste, and industrial
applications, minor representations of Na also indicates source from weathering of silicate-bearing minerals. The plot for
Na/Cl to EC indicates Na released from silicate weathering process which is also supported by higher HCO3 values in both the seasons. Ion exchange process is also activated in the study area which is indicated by shifting to right
in plot for Ca + Mg to SO4 + HCO3. The plot of Na-Cl to Ca + Mg-HCO3-SO4 confirms that Ca, Mg and Na concentrations in groundwater are derived from aquifer materials. Thermodynamic plot indicates
that groundwater is in equilibrium with kaolinite, muscovite and chlorite minerals. Saturation index of silicate and carbonate
minerals indicate oversaturation during pre-monsoon and undersaturation during post-monsoon, conforming dissolution and dilution
process. In general, water chemistry is guided by complex weathering process, ion exchange along with influence of Cl ions
from anthropogenic impact. 相似文献
11.
文章以桂林典型岩溶区和非岩溶区土壤剖面为研究对象,采用改进的Tessier元素形态连续提取法,测定岩溶区和非岩溶区土壤钙（Ca）和镁（Mg）元素离子交换态（包括水溶态）、碳酸盐结合态、腐殖酸结合态、铁锰氧化物结合态、强有机质结合态（包括部分硫化物）和残渣态等形态,探讨岩溶区和非岩溶区土壤Ca、Mg形态在土壤剖面中的迁移变化特征。结果表明:（1）岩溶区石灰土剖面中,随剖面深度加深,pH值增大,而土壤有机质、全氮（N）、全磷（P）含量减少,Ca元素主要以交换态存在且在各土壤剖面中含量相近,Mg元素主要是以残渣态赋存在土壤剖面中,随着土壤剖面深度腐殖酸结合态百分比减少,存在累积现象;（2）在非岩溶地区酸性土壤中,土壤总钙较低。在土壤剖面0~60 cm以强有机结合态为主,深层剖面（大于60 cm）以残渣态为主;Mg元素有效态含量较低,非岩溶区土壤Mg元素以腐殖酸结合态和残渣态为主,与岩溶区土壤类似,非岩溶区Mg元素在土壤中也存在一定累积。 相似文献
12.
Bo Peng Adam Piestrzynski Jadwiga Pieczonka Meilian Xiao Yaozhu Wang Shurong Xie Xiaoyan Tang Changxun Yu Zhi Song 《Environmental Geology》2007,52(7):1277-1296
The mineralogy and geochemistry of the waste rocks distributed at Taojiang Mn-ore deposit, central Hunan province, China,
were studied using X-ray powder diffraction (XRD), electron microprobe analysis (EMPA) fitted with energy dispersive spectrometer
(EDS) and inductively coupled plasma mass spectrum (atomic emission spectra) ICP-MS (AES), with the aim of predicting the
environmental impacts of weathering of the waste rocks. The mineralogical results from microscope observation and XRD and
EMPA studies show that the waste rock is composed of black shale and minor Mn carbonates. The oxidation of sulfide minerals
such as galena, pyrite and chalcopyrite is accompanied by decomposition of Mn carbonates and K-feldspar during exposure to
atmospheric O2. The geochemical characteristics of major, rare earth elements (REE) and trace elements of the waste rocks also show that
the waste rock can be divided into black shale and Mn carbonate, and both of them are currently under chemical weathering.
The major alkalies and alkaline elements (Ca, Mg, Na, K, Rb, Sr and Cs) and major elements (Fe, S and P) and heavy metals
(Sc, V, Cr, Th, U, Sn, Co, Ni, Cu, Zn, Pb, Mo, Cd, Sb, an Tl) are being released during weathering. The mobility of alkalis
and alkaline elements Ca, Mg, Na, K, Rb, Sr and Cs is controlled by decomposition of Mn carbonates. The dispersion of Cr,
Sc and Th (U) might be related to weathering of K-feldspar, and the release of the heavy metals Co, Ni, Cu, Zn, Pb, Mo, Cd
Sb and Tl is dominated by the breaking of sulfide minerals. The REE of the waste rocks and surrounding soils and the spidery
distribution patterns of heavy metals in the waste rocks, the surrounding soils and the surface waters show that weathering
of the waste rocks and bedrock might be the sources of heavy metal contamination for the surrounding soils and surface water
system for the mining area. This is predicted by the mass-balance calculation by using Zr as an immobile element. Therefore,
it is urgently necessary take measures to treat the waste rocks distributed throughout the area for the local environmental
protection. 相似文献
13.
A small watershed (160 km2) located in the Massif Central (France) has been chemically, isotopically and hydrologically studied through its dissolved load, bed sediments and soils. This watershed is underlain by basaltic bedrock and associated soils in which the vegetation is dominated mainly by meadows.Dissolved concentrations of major ions (Cl, SO4, NO3, HCO3, Ca, Na, Mg, K, Al and Si), trace elements (Rb and Sr) and strontium isotopes have been determined for two different hydrologic periods on the main stream of the Allanche river and its tributaries.The major objectives of this study were to characterize the chemical and isotopic signatures of each reservoir occurring in the watershed. Changes in chemical and isotopic signatures are interpreted in terms of fluctuations of the different components inputs: rainwater, weathering products, anthropogenic addition.Water quality may be influenced by natural inputs (rainwater, weathering processes) and anthropogenic additions (fertilizers, road salts, etc.). Precipitation serves as a major vehicle for dissolved chemical species in addition to the hydrosystem and, in order to constrain rain inputs, a systematic study of rainwaters is carried out over a one year period using an automatic collector. Corrections of rainwater addition using chloride as an atmospheric input reference were computed for selected elements and the Sr/Sr ratio. After such corrections, the geochemical budget of the watershed was determined and the role of anthropogenic additions evaluated through the relationship between strontium isotopes and major and trace element ratios. Thus, 10% of Ca and Na originate in rainwater input, 40 to 80% in fertilizer additions and 15 to 50% in rock weatheringThe cationic denudation rates for this watershed are around 0.3 g s–1 km2 during low water discharge and 0.6 g s–1 km2 in high water stage. This led to a chemical denudation rate of 5.3 mm/1000 years.For solid matter, the normalization of chemical species relative to parent rocks shows the depletion or enrichment in soils and sediments. The use of K and Ca as mobile reference illustrates the weathering state of soils and sediments relative to parent rocks. This weathering state for bed sediments range from 15 to 45% for the K normalization and from 2 to 50% for the Ca normalization. For the soils, the weathering state ranges from 15 to 57% for the K normalization and from 17 to 90% for the Ca normalization. 相似文献
14.
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. 相似文献
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17.
《Geochimica et cosmochimica acta》1999,63(23-24):4013-4035
The effect of organic matter during soil/water interaction is still a debated issue on the controls of chemical weathering in a tropical environment. In order to study this effect in detail, we focused on the weathering processes occurring in a small tropical watershed (Nsimi-Zoetélé, South Cameroon). This site offers an unique opportunity to study weathering mechanisms in a lateritic system within a small basin by coupling soil and water chemistry.The lateritic cover in this site can reach up to 40 m in depth and show two pedological distinct zones: unsaturated slope soils on the hills and/or elevated areas; and water-saturated soils in the swamp zone which represent 20% of the basin surface. The study present chemical analysis performed on water samples collected monthly from different localities between 1994–1997 and on soil samples taken during a well drilling in December 1997. The results suggest the existence of chemical and spatial heterogeneities of waters in the basin: colored waters flooding the swamp zone have much higher concentrations of both organic matter (i.e., DOC) and inorganic ions (e.g., Ca, Mg, Al, Fe, Th, Zr) than those from springs and groundwater from the hills. Nevertheless, these organic-rich waters present cation concentrations (Na, Ca, Mg, K) which are among the lowest compared to that of most world rivers. The main minerals in the soils are secondary kaolinite, iron oxi-hydroxides, quartz, and accessory minerals (e.g., zircon, rutile). We mainly focused on the mineralogical and geochemical study of the swamp zone soils and showed through SEM observations the textural characterization of weathered minerals such as kaolinite, zircon, rutile, and the secondary recrystallization of kaolinite microcrystals within the soil profile. Water chemistry and mineralogical observations suggest that hydromorphic soils of the swamp zone are responsible for almost all chemical weathering in the basin. Thus, in order to explain the increase of element concentration in the organic-rich waters, we suggest that organic acids enhance dissolution of minerals such as kaolinite, goethite, and zircon and also favors the transport of insoluble elements such as Al, Fe, Ti, Zr, and REE by chemical complexation. SiO2(aq) concentrations in these waters are above saturation with respect to quartz. Dissolution of phytholithes (amorphous silica) may be responsible for this relatively high SiO2(aq.) concentration. Al/Mg ratios obtained for the soil and the Mengong river waters show that a significant amount of Al does not leave the system due to kaolinite recrystallisation in the swamp zone soils. Geochemical data obtained for this watershed show the important contribution of vegetation and organic matter on chemical weathering in the swamp zone. Quantitatively we propose that the increasing amount in total dissolved solid (TDS) due to organic matter and vegetation effect is about 35%. In summary, this interaction between soils and waters occurs mostly in soils that are very depleted in soluble elements. Thus, the low concentration of major elements in these water is a direct consequence of the depleted nature of the soils. 相似文献
18.
贵州麻江蓝莓种植区基岩-土壤剖面元素地球化学特征 总被引：1，自引：0，他引：1
本文对麻江蓝莓核心产区种植剖面的地球化学特征进行分析,选取与蓝莓生长关系密切的K、Ca、Na、Mg、Fe、Al、Mn、Mo、Co、V、Se、Cr、Cu、Zn十四种元素作为研究对象,结果表明:土壤中元素的地球化学特征受植物根系、外援施肥、自然气候、土壤理化性质及母岩等多种因素影响。黏粒含量高的土壤剖面元素移动性较差,含量变化程度小。Se在垂直方向上的含量变化规律主要受土壤有机质含量影响,其他元素地球化学特征主要与母岩风化和淋溶作用等因素有关。基岩产状影响土壤元素在垂直方向上的变化,产状平缓的剖面各元素在下层累积较高,而基岩产状倾斜的剖面底层土壤元素随水流失,元素含量最高值大多都出现在次底层。剖面土壤中元素的地球化学特征与自然气候、土壤理化性质及母岩等因素有关,耕作层土壤元素主要受植物根系和外援施肥影响。 相似文献
19.
Sr isotope and Ca/Mg/Sr chemical compositions of freshwater ostracode tests separated from a sediment core represent the last 16 ka of sedimentation in Lake Constance, Central Europe. The chemical evolution of the paleowater's dissolved load of Lake Constance was estimated by correcting the ostracode data for Ca/Mg/Sr fractionation due to biogenic calcification. Since the Late Pleistocene deglaciation, the Ca/Sr molar ratios of paleowaters increased systematically from about 100 (a near marine signature) to about 200. Ca/Mg molar ratios varied in the range of 1–25. The 87Sr/86Sr ratios indicate Late Pleistocene paleowater compositions of 0.7086–0.7091, significantly more radiogenic than present day waters (0.7085). Sr isotopes and Ca/Mg/Sr chemical data together show that weathering of Mesozoic evaporites consistently dominated the dissolved Sr load (80–90%). Carbonate and silicate weathering were less important (1–10%). Trends of Sr dissolved loads were therefore not related to Mg which was mainly mobilized by carbonate weathering. Biotite weathering was an important source of radiogenic Sr in the paleowaters. The short-term release (duration about 600–800 years) of radiogenic Sr during glacier retreat started 15.2 ka ago and was due to enhanced biotite weathering at the glacier base. Long-term release of radiogenic Sr was due to biotite weathering in glacial soils and silicate rocks, and has gradually declined since the Late Pleistocene/Holocene transition. 相似文献
20.
The detailed hydro-chemical study of meltwater draining from Khangri glacier Arunachal Pradesh has been carried out to evaluate the major ion chemistry and weathering processes in the drainage basin. The investigative results shows that the meltwater is almost neutral to slightly acidic in nature with Mg–HCO3-dominated hydro-chemical facies. In glacial meltwater, Ca+?2 is the most dominated cation followed by Mg+2, Na+, and K+, while HCO3? is the most dominant anion followed by SO42?, NO3?, and Cl?. The dominant cations such as Ca+2 and Mg+2 show a good relation with the minerals abundance of the rocks. Calcite (CaCO3) and biotite [K(Mg,Fe)3AlSi3O10(F,OH)2] are the most abundant minerals in the deformed carbonate-rich metasedimentary rocks near to the snout with some K feldspar (KAlSi3O8) and quartz (SiO2). This suggests Ca+2 have definitely entered into the water due to the dissolution of calcite and Ca feldspar (CaAl2Si2O8), while one of the source of Mg+2 is biotite. Na feldspar (NaAlSi3O8) has contributed towards the availability of sodium ion, while potassium ion is derived from the chemical weathering of K feldspar and biotite. The chemical weathering is the foremost mechanism controlling the hydro-chemistry of the Khangri glacier because of the least anthropogenic interferences. The mineralogy of surrounding rocks is studied to understand better, the rock–water interaction processes, and their contribution towards ionic concentration of meltwater. The meltwater discharge and individual ion flux of the catchment area have also been calculated, to determine the ionic denudation rate for the ablation season. The high elemental ratio of (Ca?+?Mg)/(Na?+?K) (7.91?±?0.39 mg/l) and low elemental ratio of (Na?+?K)/total cations (0.11?±?0.004) indicate that the chemical composition of meltwater is mainly controlled by carbonate weathering and moderately by silicate weathering. The scatter plot result between (Ca?+?Mg) and total cations confirms that carbonate weathering is a major source of dissolved ions in Khangri glacier meltwater. In addition, the statistical analysis was also used to determine the correlation between physical parameters of glacier meltwater which controlled the solute dynamics. 相似文献