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1.
 Adsorption/desorption and oxidation/reduction of arsenic at clay surfaces are very important to the natural attenuation of arsenic in the subsurface environment. Although numerous studies have concluded that iron oxides have high affinities for the adsorption of As(V), very little experimental work has addressed the arsenic attenuation capacities of different clay minerals and aging process affecting the transformation of arsenic. The abundance of clay minerals in a variety of geochemical environments and their influence on adsorption of contaminants suggests a need for more experimental work to characterize the adsorption desorption, and oxidation of arsenic on clay minerals. In this investigation three types of clay mineral were studied: the 1 : 1 layer clays [halloysite (IN), sedimentary M-kaolinite, and weathered EPK-kaolinite]; the 2 : 1 layer clays [illite (MT) and illite/montmorillonite (MT)]; the 2 :>: 1 layer clay [chlorite (CA)]. The halloysite and the chlorite had much greater As(V) adsorption (25–35 folds) than the other clay minerals. The clay minerals had lower As(III) adsorption than As(V) adsorption, and the adsorption was affected by pH. Desorption of arsenic from the clay minerals was significantly influenced by the aging process. The quantities of extractable As(III) and As(V) decreased with increasing aging time. The results demonstrated that oxidation of As(III) to As(V) occurred on the clay surfaces, whereas reduction of As(V) to As(III) was not found in any of the clay minerals studied. The oxidation of As(III) was affected by the types of clay and aging time. Received: 22 March 1999 · Accepted: 15 April 1999  相似文献   

2.
The eastern limb of horse shoe shaped “Bonai Synclinorium” in India hosts Banded Iron Formations (BIFs), consisting of major high grade iron deposits. Phosphorus (P) gets adsorbed in the iron ore by way of ion exchange mechanism of clay minerals and hydrated secondary iron oxide minerals. Its concentration is lesser in hard ores and blue dust types of ores, while the highest in case of lateritic ores. P content reduces with increase in iron (Fe) content in individual ore types. Along the eastern limb, phosphorus content gradually reduces from north to south direction. Since phosphorus is mainly associated with secondary lateritization process, its concentration is very high in top weathered profile and along the weaker zones.  相似文献   

3.
Undisturbed core samples of Recent sediments from the Wash tidal flats, East Anglia, England, obtained using a Delft corer, were studied with special reference to the diagenesis and geochemical behaviour of iron. The Mössbauer effect in 57Fe was used to monitor the distribution of Fe between different phases as a function of depth, together with the magnetic mineralogy and palaeomagnetic properties.The cores consist of, successively downwards: 0.36 m brown clay; 1.5 m finely laminated silts and fine sands, and 7.14 m homogeneous fine sands. The dominant minerals are quartz, feldspar, calcite and clay minerals, and chemical analysis for Al, Si, Mg, Mn, Ca, Fe, Na, K showed variations closely linked to lithological changes. Illite is the most abundant clay mineral (mean 48%), followed by mixed layer illite-montmorillonite and montmorillonite, kaolinite and chlorite. Chlorite is the major iron-bearing clay mineral and represents 4 to 10% of the <2 μm fraction throughout the core. Sulphide minerals are present throughout the core, including framboidal pyrite.Computer fit analysis of the Mössbauer spectra of best quality showed contributions from Fe2+ and Fe3+ in clay minerals (essentially chlorite), low-spin Fe2+ in pyrite, and magnetically ordered iron in greigite (Fe3S4). Systematic variations, as a function of sample depth, indicate a relative increase in the amount of Fe in pyrite at the expense of the clay minerals.Magnetite and titanium-bearing magnetite are the carriers of natural magnetic remanence in these sediments.The direction and intensity of natural remanence in the samples compare well with the known secular variation of the Earth's magnetic field derived from the historic-archaeomagnetic record and this enables the samples to be dated and sedimentation rates to be determined (1.5 mm yr?1 for the upper 2 m and ~7.7 mm yr?1 for the lower 7 m).  相似文献   

4.
The relationship between composition and physical parameters such as specific surface area, cationic exchange capacity and plasticity is studied with the aim of developing regression models that would permit the prediction of clay properties. These models could be useful for mineralogists and industrial applications. Nineteen representative clay samples were collected from Jebel Ressas in north-eastern Tunisia. Mineralogical data show that clay samples cover a very large variety of minerals. The main clay mineral is illite (50–60 wt%), secondary minerals including quartz, calcite and minor amounts of Na-feldspar. This study reveals that the average amount of silica (SiO2) and alumina (Al2O3) are 51.9 and 19.6 wt%, respectively. The contents of lime (CaO) and iron (Fe2O3) vary between 4 and 8 wt% whereas the amount of alkalis (Na2O + K2O) is on average 4.1 wt%. The grain size data indicates a significant amount of silt fraction, and the fraction <2 µm varies between 23 and 35 wt%. Values for plasticity index range from 16 to 28 wt%. The cation exchange capacity and the specific surface values are 34.1–45.7 meq/100 g of air-dried clay and 302–374 m2/g, respectively. Lastly, regression models are used to correlate the properties with the mineralogical and chemical compositions. The significance and the validity of models were confirmed by statistical analysis and verification experiments. The regression models can be used to select the clay properties (plasticity index, cation exchange capacity and specific surface) in relation with clay minerals proportions and the finer fraction amounts.  相似文献   

5.
The saturation index of clay minerals like Gibbsite, Kaolinite, Illite, Montmorillonite and Chlorite in groundwater were studied in detail by collecting 29 groundwater samples from the shallow coastal aquifers in and around Kalpakkam. The samples collected were analysed for major cations, anions and trace elements by using standard procedures. The study reveals that pH has a significant role in the saturation index (SI) of minerals. It also shows that the relationship of electrical conductivity to the SI of these minerals is not significant than that of the ionic strength, log pCO2 values, and alumina silica ratio have significant relation to the SI of these clay minerals. The SI of these clay minerals was spatially distributed to identify the areas of higher SI. Silica has good correlation to SI of Kaolinite, Gibbsite and Montmorillonite and Al has good correlation to SI of all the minerals except to that of Chlorite.  相似文献   

6.
Summary ?Sheet silicates of the serpentine–kaolin-group (serpentine, kaolinite, dickite, nacrite, halloysite), the talc–pyrophyllite-group (talc, pyrophyllite), the smectite-group (montmorillonite), and illite (as a mineral of the mica-group) were investigated to obtain information concerning their cathodoluminescence behaviour. The study included analyses by cathodoluminescence (CL microscopy and spectroscopy), electron paramagnetic resonance (EPR), X-Ray diffraction (XRD), scanning electron microscopy (SEM) and trace element analysis. In general, all dioctahedral clay minerals exhibit a visible CL. Kaolinite, dickite, nacrite and pyrophyllite have a characteristic deep blue CL, whereas halloysite emission is in the greenish-blue region. On the contrary, the trioctahedral minerals (serpentine, talc) and illite do not show visible CL. The characteristic blue CL is caused by an intense emission band around 400 nm (double peak with two maxima at 375 and 410 nm). EPR measurements indicate that this blue emission can be related to radiation induced defect centres (RID), which occur as electron holes trapped on apical oxygens (Si–O centre) or located at the Al–O–Al group (Al substituting Si in the tetrahedron). Additional CL emission bands were detected at 580 nm in halloysite and kaolinite, and between 700 and 800 nm in kaolinite, dickite, nacrite and pyrophyllite. Time-resolved spectral CL measurements show typical luminescence kinetics for the different clay minerals, which enable differentiation between the various dioctahedral minerals (e.g. kaolinite and dickite), even in thin section. Received December 3, 2001; revised version accepted February 27, 2002  相似文献   

7.
99Technetium (99Tc) is a fission product of uranium-235 and plutonium-239 and poses a high environmental hazard due to its long half-life (t1/2 = 2.13 × 105 y), abundance in nuclear wastes, and environmental mobility under oxidizing conditions [i.e., Tc(VII)]. Under reducing conditions, Tc(VII) can be reduced to insoluble Tc(IV). Ferrous iron, either in aqueous form (Fe2+) or in mineral form [Fe(II)], has been used to reduce Tc(VII) to Tc(IV). However, the reactivity of Fe(II) from clay minerals, other than nontronite, toward immobilization of Tc(VII) and its role in retention of reduced Tc(IV) has not been investigated. In this study the reactivity of a suite of clay minerals toward Tc(VII) reduction and immobilization was evaluated. The clay minerals chosen for this study included five members in the smectite-illite (S-I) series, (montmorillonite, nontronite, rectorite, mixed layered I-S, and illite), chlorite, and palygorskite. Surface Fe-oxides were removed from these minerals with a modified dithionite-citrate-bicarbonate (DCB) procedure. The total structural Fe content of these clay minerals, after surface Fe-oxide removal, ranged from 0.7% to 30.4% by weight, and the structural Fe(III)/Fe(total) ratio ranged from 45% to 98%. X-ray diffraction (XRD) and Mössbauer spectroscopy results showed that after Fe oxide removal the clay minerals were free of Fe-oxides. Scanning electron microscopy (SEM) revealed that little dissolution occurred during the DCB treatment. Bioreduction experiments were performed in bicarbonate buffer (pH-7) with structural Fe(III) in the clay minerals as the sole electron acceptor, lactate as the sole electron donor, and Shewanella putrefaciens CN32 cells as a mediator. In select tubes, anthraquinone-2,6-disulfate (AQDS) was added as electron shuttle to facilitate electron transfer. In the S-I series, smectite (montmorillonite) was the most reducible (18% and 41% without and with AQDS, respectively) and illite the least (1% for both without and with AQDS). The extent and initial rate of bioreduction were positively correlated with the percent smectite in the S-I series (i.e., layer expandability). Fe(II) in the bioreduced clay minerals subsequently was used to reduce Tc(VII) to Tc(IV) in PIPES buffer. Similar to the trend of bioreduction, in the S-I series, reduced NAu-2 showed the highest reactivity toward Tc(VII), and reduced illite exhibited the least. The initial rate of Tc(VII) reduction, after normalization to clay and Fe(II) concentrations, was positively correlated with the percent smectite in the S-I series. Fe(II) in chlorite and palygorskite was also reactive toward Tc(VII) reduction. These data demonstrate that crystal chemical parameters (layer expandability, Fe and Fe(II) contents, and surface area, etc.) play important roles in controlling the extent and rate of bioreduction and the reactivity toward Tc(VII) reduction. Reduced Tc(IV) resides within clay mineral matrix, and this association could minimize any potential of reoxidation over long term.  相似文献   

8.
Soil pollution by arsenic is a serious environmental problem in many mining areas. Quick identification of the amount and extent of the pollution is an important basis for developing appropriate remediation strategies. In a case study, 55 soil samples were collected from a highly heterogeneous waste dump around the Sarcheshmeh copper mine, south east Iran. Samples’ visible and near-infrared (VNIR) reflectance spectra were measured, transformed to absorbance and then pre-processed using Savitzky–Golay first-derivative (FD) and Savitzky–Golay second-derivative (SD) transformation methods. The obtained spectra were then subjected to three regression models including principal component regression (PCR), partial least squares regression (PLSR) and support vector regression (SVR) for predicting arsenic concentration. The best prediction accuracies were obtained by SVR and PLSR methods applied on first-derivative pre-processed spectra with R 2 values of 0.81 and 0.69, respectively. It was found that VNIR spectroscopy is a successful method for predicting As concentration in contaminated soils of the dumpsites. Study of the prediction mechanism showed that the intercorrelation between arsenic and spectral features of soil including iron oxy/hydroxides and clay minerals was the major mechanism enabling the prediction of arsenic concentration. However, higher values of correlation coefficients at ~460, ~560 and ~590 nm suggested the internal association between arsenic and iron minerals as the more important mechanism for prediction. This conclusion supported previous speciation studies conducted in the same waste dump using improved correlation analysis and chemical sequential extraction method.  相似文献   

9.
Salt exposures and weathering residuum on several salt diapirs in different geographic/climatic settings were studied. Anhydrite, gypsum, hematite, calcite, dolomite, quartz, and clay minerals are the main constituents of the weathering residuum covering the salt diapirs in various thicknesses. Erosion rates of residuum as well as of rock salt exposures were measured at selected sites for a period of 5 years by plastic pegs as benchmarks. Recorded data were standardized to a horizontal surface and to long-term mean precipitation. For the rock salt exposures the following long-term denudation rates were determined of 30–40 mm a−1 for coastal diapirs and up to 120 mm a−1 for mountain salt diapirs. Long-term mean superficial denudation rate measured on weathering residuum of low thickness reached 3.5 mm a−1 on coastal diapirs. The total denudation rate estimated for the thin residuum is close to 4–7 mm a−1 based on apparent correlation with the uplift rate on Hormoz and Namakdan diapirs. Denudation of rock salt exposures is much faster compared to parts of diapirs covered by weathering residuum. The extent of salt exposures is an important factor in the morphological evolution of salt diapirs as it can inhibit further expansion of the diapir. Salt exposures produce huge amounts of dissolved and clastic load, thus affecting the surrounding of the diapir.  相似文献   

10.
This study presents a methodology for siting municipal solid waste landfills, coupling geographic information systems (GIS), fuzzy logic, and multicriteria evaluation techniques. Both exclusionary and non-exclusionary criteria are used. Factors, i.e., non-exclusionary criteria, are divided in two distinct groups which do not have the same level of trade off. The first group comprises factors related to the physical environment, which cannot be expressed in terms of monetary cost and, therefore, they do not easily trade off. The second group includes those factors related to human activities, i.e., socioeconomic factors, which can be expressed as financial cost, thus showing a high level of trade off. GIS are used for geographic data acquisition and processing. The analytical hierarchy process (AHP) is the multicriteria evaluation technique used, enhanced with fuzzy factor standardization. Besides assigning weights to factors through the AHP, control over the level of risk and trade off in the siting process is achieved through a second set of weights, i.e., order weights, applied to factors in each factor group, on a pixel-by-pixel basis, thus taking into account the local site characteristics. The method has been applied to Evros prefecture (NE Greece), an area of approximately 4,000 km2. The siting methodology results in two intermediate suitability maps, one related to environmental and the other to socioeconomic criteria. Combination of the two intermediate maps results in the final composite suitability map for landfill siting.  相似文献   

11.
The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.  相似文献   

12.
 A thorough understanding of the characteristics of transmissivity makes groundwater deterministic models more accurate. These transmissivity data characteristics occasionally possess a complicated spatial variation over an investigated site. This study presents both geostatistical estimation and conditional simulation methods to generate spatial transmissivity maps. The measured transmissivity data from the Dulliu area in Yun-Lin county, Taiwan, is used as the case study. The spatial transmissivity maps are simulated by using sequential Gaussian simulation (SGS), and estimated by using natural log ordinary kriging and ordinary kriging. Estimation and simulation results indicate that SGS can reproduce the spatial structure of the investigated data. Furthermore, displaying a low spatial variability does not allow the ordinary kriging and natural log kriging estimates to fit the spatial structure and small-scale variation for the investigated data. The maps of kriging estimates are smoother than those of other simulations. A SGS with multiple realizations has significant advantages over ordinary kriging and even natural log kriging techniques at a site with a high variation in investigated data. These results are displayed in geographic information systems (GIS) as basic information for further groundwater study. Received: 27 August 1999 · Accepted: 22 February 2000  相似文献   

13.
李哲  李仁伟 《岩石学报》1989,5(1):21-27
东濮盆地四口井的25个沉积岩样品的穆斯堡尔谱学研究结果表明,沉积岩样品中的主要含铁矿物相为黄铁矿、粘土矿物以及一些碳酸盐矿物。沉积岩中黄铁矿铁的相对含量与Pr/Ph和CPI之间存在着负相关关系,表明穆斯堡尔谱学方法所确定的黄铁矿铁的相对含量可以作为沉积岩形成时古环境分析的一项可靠指标。此外,东濮盆地铁白云石主要分布在一定深度范围之内,本文讨论了铁白云石的分布与沉积岩有机质成熟度之间的对应关系。  相似文献   

14.
The Nkout deposit is part of an emerging iron ore province in West and Central Africa. The deposit is an oxide facies iron formation comprising fresh magnetite banded iron formation (BIF) at depth, which weathers and oxidises towards the surface forming caps of high grade hematite/martite–goethite ores. The mineral species, compositions, mineral associations, and liberation have been studied using automated mineralogy (QEMSCAN®) combined with whole rock geochemistry, mineral chemistry and mineralogical techniques. Drill cores (saprolitic, lateritic, BIF), grab and outcrop samples were studied and divided into 4 main groups based on whole rock Fe content and a weathering index. The groups are; enriched material (EM), weathered magnetite itabirite (WMI), transitional magnetite itabirite (TMI) and magnetite itabirite (MI). The main iron minerals are the iron oxides (magnetite, hematite, and goethite) and chamosite. The iron oxides are closely associated in the high grade cap and liberation of them individually is poor. Liberation increases when they are grouped together as iron oxides. Chamosite significantly lowers the liberation of the iron oxides. Automated mineralogy by QEMSCAN® (or other similar techniques) can distinguish between Fe oxides if set up and calibrated carefully using the backscattered electron signal. Electron beam techniques have the advantage over other quantitative mineralogy techniques of being able to determine mineral chemical variants of ore and gangue minerals, although reflected light optical microscopy remains the most sensitive method of distinguishing closely related iron oxide minerals. Both optical and electron beam automated mineralogical methods have distinct advantages over quantitative XRD in that they can determine mineral associations, liberation, amorphous phases and trace phases.  相似文献   

15.
 The interaction of γ-rays with smectites induces paramagnetic defects in the structure of these clay minerals. The EPR spectra of three different smectites detect the creation of structural defects and trapping of organic free radicals in the clay structure upon irradiation. The defects are assigned to positive holes or trapped electrons stabilised by existing local charge imbalances in the mineral lattice. The organic radicals are derived from organic compounds present as impurities in the crystal lattice of the clay minerals. In addition, γ-rays cause migration of small interlayer cations (such as Li+) into the layers, as clearly evidenced by EPR and FT-IR reflectance spectroscopies. Received: 20 April 2000 / Accepted: 2 December 2000  相似文献   

16.
An investigation on spatial distribution, possible pollution sources, and affecting factors of heavy metals in the urban–suburban soils of Lishui city (China) was conducted using geographic information system (GIS) technique and multivariate statistics. The results indicated that the topsoils in urban and suburban areas were enriched with metals, such as Cd, Cu, Pb, and Zn. Spatial distribution maps of heavy metal contents, based on geostatistical analysis and GIS mapping, indicated that Cd, Cr, Cu, Mn, Ni, Pb, and Zn had similar patterns of spatial distribution. Their hot-spot areas were mainly concentrated in the densely populated old urban area of the city. Multivariate statistical analysis (correlation analysis, principal component analysis, and clustering analysis) showed distinctly different associations among the studied metals, suggesting that Cr, Cu, Ni, Pb, Cd, and Zn had anthropogenic sources, whereas Co and V were associated with parent materials and therefore had natural sources. The Cd, Cr, Ni, Pb, and Zn contents were positively correlated with soil organic matter, pH, and sand content (p < 0.01). It is concluded that GIS and multivariate statistical methods can be used to identify hot-spot areas and potential sources of heavy metals, and assess soil environment quality in urban–suburban areas.  相似文献   

17.
鞍山-本溪条带状铁建造(Banded Iron Formation,简称BIF)位于华北克拉通东北缘,是世界上典型BIF之一,也是我国最重要的铁矿资源基地。大孤山位于鞍山地区南部矿带,为新太古代典型的Algoma型BIF,与华北克拉通其它大多数BIF相比,具有较低变质程度(绿片岩相-低角闪岩相)和较完整的沉积相分布特征。因此,通过大孤山BIF的研究有利于追踪Algoma型BIF的原生矿物组成及其后期成岩-变质过程,进而通过分析原生矿物形成的物理化学条件探讨古海洋环境。依据原生矿物共生组合及产出特征,可将大孤山BIF沉积相划分为氧化物相(30%)、硅酸盐相(50%)和碳酸盐相(20%)。氧化物相主要分布于主矿体南部,主要矿物组成为磁铁矿和石英;硅酸盐相分布于主矿体中部,主要矿物组成除了石英和磁铁矿之外,还有黑硬绿泥石、绿泥石、镁铁闪石等;碳酸盐相分布于矿体北部,主要矿物组成为菱铁矿、磁铁矿和石英等。本文通过大孤山BIF岩相学观察和含铁矿物化学成分研究,推测原生沉积物的组成为无定形硅胶、三价铁氢氧化物和富铝粘土碎屑,在经历了成岩和低级变质作用后转变为具不同相带的条带状铁建造。通过分析磁铁矿、菱铁矿和黑硬绿泥石等矿物在不同P_(O_2)-P_(CO_2)和pH-Eh条件下的共生相图可知,这些矿物均是在较低氧逸度、中到弱碱性环境下形成。综合考虑矿物成分、共生组合及受变质作用较弱等信息,本文推测制约原生矿物形成的控制因素主要是古海水氧化还原状态、酸碱度、CO_2含量和硫逸度。  相似文献   

18.
Oxygen isotopic compositions of clay minerals were determined on representative samples of the volcano-sedimentary series from Site 841 ODP (Tonga forearc). This isotopic study has demonstrated an abnormally high crystallisation temperature of the clay minerals with respect to temperature expected in burial diagenesis. Formation temperatures obtained using 18O reach up to 200 °C in a Fe-chlorite-corrensite paragenesis found in the vicinity of basaltic andesite sills intruded into the Miocene tuffs. The paleothermal flux resulting from the cooling of the sills has produced very low grade contact metamorphism in the Miocene Tonga forearc deposits. The consequence of this was the formation of a large amount of hydrous silicates characterised near the sills by a Fe-clays-analcime mineralogical association. Received: 26 September 1997 / Accepted: 22 September 1998  相似文献   

19.
Industrial development has increased fast in China during the last decades. This has led to a range of environmental problems. Deposition of trace elements to forest ecosystems via the atmosphere is one potential problem. In this paper, we report the results from a pilot study where the trace element levels of the sub-alpine forest soils on the eastern edge of the Tibetan Plateau have been measured. Possible relationships between soil properties and trace element concentrations have also been investigated. The obtained concentrations (mg kg−1) were boron (B) 48.06–53.70, molybdenum (Mo) 1.53–2.26, zinc (Zn) 68.18–79.53, copper (Cu) 36.81–42.44, selenium (Se) 0.33–0.49, cadmium (Cd) 0.16–0.29, lead (Pb) 25.80–30.71, chromium (Cr) 96.10–110.08, nickel (Ni) 30.16–45.60, mercury (Hg) 0.05–0.11, and arsenic (As) 3.09–4.17. With a few exceptions, the element concentration can be characterized as low in the investigated sub-alpine forest soils. No clear differences in trace element levels were found between topsoil and subsoil samples, indicating that the atmospheric deposition of trace element has been low. The soil parent material plays a key role to determine trace element levels. Soil properties, including pHw, organic carbon (OC), clay fraction, cation-exchange capacity (CEC), total iron (Fe), and total aluminum (Al) concentrations were related to trace element concentration using correlation analysis. Total Fe and Al showed the strongest relationships with concentrations of most trace elements in the sub-alpine forest soils. PCA analyses indicated that a significant increase in the number of cars with the fast development of local tourism may result in higher Pb concentration in the future.  相似文献   

20.
Soil organic matter is known to contain a stable fraction with an old radiocarbon age. Size and stabilisation processes leading to the formation of this old soil carbon pool are still unclear. Our study aims to differentiate old organic matter from young and labile carbon compounds in two acid forest soils (dystric cambisol, haplic podzol). To identify such fractions soil samples were exposed to oxidation with Na2S2O8 and to dissolution by hydrofluoric acid (HF). A negative correlation between 14C activity and carbon release after dissolution of the mineral matrix by HF indicates a strong association of stabilised carbon compounds with the mineral phase. A negative correlation between the 14C activity and the relative proportion of carbon resistant to oxidation by Na2S2O8 shows that young carbon is removed preferentially by this treatment. The fraction remaining after oxidation represents a certain stabilised, long residence time carbon pool. This old fraction comprises between 1 and 30% of the total soil organic carbon in the surface horizons, but reaches up to 80% in the sub-surface horizons. Old OC is mainly stabilised by organo-mineral associations with clay minerals and/or iron oxides, whereas intercalation in clay minerals was not found to be important.  相似文献   

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