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1.
The problem of using surface geochemical exploration techniques in areas of very thick and electrically conductive weathering residuum is common to much of Australia. At the Elura deposit (New South Wales) a distinct electrogeochemical H+ anomaly can be detected in the top few cm of residual soil above about 100 m of conductive residual overburden. In the present paper the results of an investigation of the much more difficult problem of detecting sulfide mineralization beneath thick conductive transported overburden are described.The objective of the study was to demonstrate that sulfide mineralization beneath thick transported overburden can be detected by geochemical patterns in surface soils in the context of an electrogeochemical model of dispersion.The Thalanga massive sulfide deposit in northeast Queensland has at least 4 million tonnes of 15% combined Zn, Pb and Cu. The mineralized horizon lies at the contact between rhyolitic and dacitic rocks of the Cambro-Ordovician Mt. Windsor Volcanics. The deposit is covered by transported cemented Tertiary terrigenous clayey sandstones and grits; these are electrically conductive and vary in thickness from 0 to 70 m.Near-surface soil samples were collected along five traverses normal to the strike of mineralization. The traverses were located to give 0 m, 1 m, 30 m, 50 m, and 70 m overburden thicknesses; there is no known significant mineralization along the last traverse which is assumed to be background, and there is a small gossan where the overburden is absent.Dispersion patterns influenced by electrogeochemical processes should result in relatively low values for ions over massive sulfides with lateral peaks; this has been termed a “rabbit-ear” anomaly. “Rabbit-ear” anomalies in surface soils for H+, Cu, and Zn occur over the sulfide zone. The H+ pattern is better defined where there is a significant depth of overburden (where the anomaly is about 500 m wide). The Cu anomaly is 300–600 m wide, and the Zn anomaly is 450–675 m wide.Even where the overburden is 50 m thick, anomalous “rabbit-ear” anomalies for H+ and Zn are clearly identifiable, but the anomaly for Cu is a single peak of 20 ppm over the hanging wall. It is suggested that the results of this work convincingly demonstrate that at Thalanga surface soil samples may reliably be used to detect massive sulfide deposits - even where they are effectively blind beneath a considerable thickness of transported and conductive overburden. The processes of dispersion are speculated to be diffusion, and it is argued that the pattern-controlling mechanism is electrochemical.  相似文献   

2.
An assessment is made of the use of lead isotopes in soils as an exploration tool for concealed lead-rich base metal massive sulphide deposits, using four case histories in southeast Australia as examples. Case history 1 covers soil profiles (< 1 m depth) unrelated to mineralization in which the lead isotope ratios exhibit variation with depth and are different from those for massive sulphide deposits. Case history 2 covers six shallow (< 0.4 m depth) profiles from two traverses over the concealed Elura Zn-Pb-Ag deposit in central western New South Wales. For one traverse over completely concealed (blind) sulphides, no isotopic or geochemical signature of the orebody could be detected. In two profiles from the other traverse, for depths of 0.15 m and 0.3–0.45 m, the lead isotopic ratios in the soils are identical with those in the ore (the target isotope ratios). Case history 3 covers two occurrences of Silurian volcanogenic Cu-Zn-Pb mineralization at the Benambra prospect in northeast Victoria. The isotopic ratios for the soils are identical with those in the sulphides and the isotopic signature of the sulphides is also detectable in traverses where no obvious surface anomaly is developed. Case history 4 is an undrilled anomaly in Silurian shales and felsic volcanics where the isotope ratios in B horizon soils are consistent with those of the target isotopic signature.The information from these case histories suggests that the lead isotopic analysis of soils will be a useful exploration tool for concealed mineralization, although at the present stage of research it appears that its application may be limited to shallowly buried (< 100 m) targets or deeply buried targets with an extensive oxidation profile. Its main advantage over conventional geochemical techniques is its ability to discriminate between similar geochemical anomalies arising from different styles of mineralization, as illustrated by an example from Benambra.  相似文献   

3.
《Applied Geochemistry》2005,20(1):169-178
A sampling-separation method and a dynamic monitoring method were used to investigate the time-dependent reactions of H+ ions with two contrasting types of soil, variable charge soils (VCS) and constant charge soils (CCS), by directly evaluating H+ ion consumption and other relevant consequences. The results for both CCS and VCS show that H+ ion consumption, increase in positive surface charge and increase in soluble Al are all characterized by a rapid step followed by a slow one. The higher the content of free Fe oxides in the soil, the larger the increase in positive surface charge and in H+ ion consumption in the initial rapid step. This is due mainly to protonation on external surfaces. The gradual increase in positive surface charge in the slow step for the 3 VCSs is a result of H+ ion diffusion to the reactive sites of Fe–OH on internal surfaces. The very low content of free Fe oxides on internal surfaces of the 2 CCSs render a negligible increase in positive surface charge in the slow step. For the 3 VCSs, the gradual consumption of H+ ions in the slow process is the result of protonation, Al dissolution and/or transformation into exchangeable acidity. For the 2 CCSs, however, the gradual consumption is mainly the result of Al dissolution and/or transformation into exchangeable acidity. The time-dependent Al dissolution from both VCS and CCS is influenced by several factors such as mineral components, solubility and dissolution rates of the soils, and H+ ion concentration in soil suspensions.  相似文献   

4.
The oxidation of the iron sulfide, pyrite, in acid sulfate soil floodplains generate substantial acidity and this acid has caused further weathering of the soil profile. The movement of groundwater from these soils is an important geochemical control on surface water quality. The flux of acidified and metal-rich water during a wet season rainfall event has been examined at two study catchments on the Tweed River in eastern Australia. At the sites, 81 kg/ha and 60 kg/ha of oxidisable acidity are exported, along with Al, Fe and Zn during the flood event. The main contributors to the acid flux are H+, Fe and Al at the first site and whilst Fe and Al are present in the drainage waters at the second site, the main contributor is likely to be H+. The different flux characteristics at the sites may be caused by different surface soil hydraulic conductivities and oxidation history.  相似文献   

5.
This study focused on the chemical compositions of the rivers around Yulong Mountain, one of the typical monsoonal temperate glacier regions in China. Water samples were collected from Baishui, Sanshu and Geji hydrological stations around Mt. Yulong during rainy season. The chemical analyses indicated that the river water around Mt. Yulong was characterized by high pH values (>8.0) and EC values varied from 36.4 to 71.7 μS/cm with an average of 52.6 μS/cm. Ca2+ and Mg2+ were the dominant cations, together accounting for about 90 % of the total cations. HCO3 ?, followed by SO4 2?, was the dominant anion. Obvious variations had been perceived during the rainy season. River water chemistry in rainy season was mainly influenced by precipitation and rock weathering. The proportions of Na+, K+, Ca2+, Mg2+ and SO4 2? from precipitation in river water were 23.44, 9.66, 3.10, 17.81 and 10.48 %, respectively. In addition, the ion characteristics of river water were mainly influenced by carbonate weathering. The human activities should not be ignored though its influence was little.  相似文献   

6.
Volcanic‐hosted massive sulfide (VHMS) deposits of the eastern Lachlan Fold Belt of New South Wales represent a VHMS district of major importance. Despite the metallogenic importance of this terrane, few data have been published for sulfur isotope distribution in the deposits, with the exception of previously published studies on Captains Flat and Woodlawn (Captains Flat‐Goulburn Trough) and Sunny Corner (Hill End Trough). Here is presented 105 new sulfur isotope analyses and collation of a further 92 analyses from unpublished sources on an additional 12 of the VHMS systems in the Hill End Trough. Measured δ34S values range from ‐7.4% to 38.3%, mainly for massive and stockwork mineralisation. Sulfur isotope signatures for polymetallic sulfide mineralisation from the Lewis Ponds, Mt Bulga, Belara and Accost deposits (group 1) are all very similar and vary from ‐1.7% to 5.9%. Ore‐forming fluids for these deposits were likely to have been reducing, with sulfur derived largely from a magmatic source, either as a direct magmatic contribution accompanying felsic volcanism or indirectly through dissolution and recycling of rock sulfide in host volcanic sequences. Sulfur isotope signatures for sulfide mineralisation from the Calula, Commonwealth, Cordillera and Kempfield deposits, Peelwood mine and Sunny Corner (group 2) are similar and have average δ34S values ranging from 5.4% to 8.1%. These deposits appear to have formed from ore fluids that were more oxidising than group 1 deposits, representing a mixed contribution of sulfur derived from partial reduction of seawater sulfate, in addition to sulfur from other sources. The δ34S values for massive sulfides from the John Fardy deposit are the highest in the present study and have a range of 11.9–14.5%, suggesting a greater component of sulfur of seawater origin compared to other VHMS deposits in the Hill End Trough. For barite the sulfur isotope composition for samples from the Commonwealth, Stringers and Kempfield deposits ranges from 12.6% to 38.3%. More than 75% of barite samples have a sulfur isotope composition between 23.4 and 30.6%, close to the previously published estimates of the composition of seawater sulfate during Late Silurian to earliest Devonian times, providing supporting evidence that these deposits formed concurrently with the Late Silurian volcanic event. Sulfur isotope distribution appears to be independent of the host rock unit, although there appears to be a relation linking the sulfur isotope composition of different deposits to defined centres of felsic volcanism. The Mt Bulga, Lewis Ponds and Accost systems are close to coherent felsic volcanic rocks and/or intrusions and have sulfur isotope signatures with a stronger magmatic affinity than group 2 deposits. By contrast, group 2 deposits (including John Fardy) are characterised by 34S‐enrichment and a lesser magmatic signature, are generally confined to clastic units and reworked volcanogenic sediments with lesser coherent volcanics in the local stratigraphy, and are interpreted to have formed distal from the magmatic source. An exception is the Belara deposit, which is hosted by reworked felsic volcanic rocks and has a more pronounced magmatic sulfur isotope signature.  相似文献   

7.
Major ions showed high concentrations, ionic strength and chemical activity in the surface waters of Govind Ballabh Pant Sagar reservoir. Various geochemical ratios showed the dominance of silicate over carbonate weathering and major ions such as Na+ + K+ account for about 52 % of the cation budget. The high Na+ and K+ showed sedimentation of rock/coal particles consisting of highly weathered silicate minerals contributed by the discharge of mine water, fly ash mixing during transportation, etc. Further, Ca2+ + Mg2+/Na+ + K+ ratio was <1 (0.92) indicating the occurrence of silicate weathering in the reservoir catchment. The comparative assessment showed that the proportion of Ca2+ + Mg2+/Na+ + K+ tends to be lower along the coal mining belts compared to non-coal mining regions in the world. The Ca2+/SO4 2? ratio <1 revealed not only H2CO3 but H2SO4 also acting as a source of protons for rock weathering. The cause underlying these differences can be related directly to geological substrate and anthropogenic activities.  相似文献   

8.
A simple, unifying approach to classifying quantitatively the susceptibility of catchment soils and surface waters to acidification is suggested. In areas subject to a strong maritime influence, such as the UK and substantial parts of NW Europe, wherever soil mineral weathering rates are low and soils are unfertilised, atmospherically derived base cations of maritime origins have a greater effect than those derived from biogeochemical weathering on the exchangeable soil base cations. This is directly reflected in the relative base cation concentrations of the associated drainage waters, which become increasingly Na-dominated. Using 10 sub-catchments of the River Dee in north-eastern Scotland, it is shown here that the extent of Na dominance, the ratio of Na+ to ΣNa++Ca2++Mg2+, at any point in a river provides a quantitative index of the upstream weathering rate and thus of the susceptibility of the river concerned to acidification under diverse flow conditions. Data from a further 58 sub-catchments from the same river system, and from 4 other catchments from around Scotland, were used to validate this theory.  相似文献   

9.
Microscopic and spectroscopic studies were conducted to assess mineral transformation processes in aqueous suspensions of illite (Il), vermiculite (Vm) and montmorillonite (Mt) that were subjected to weathering in a simulated high-level radioactive tank waste leachate (0.05 m AlT, 2 m Na+, 1 m NO3−, pH ∼14, Cs+ and Sr2+ present as co-contaminants). Time series (0 to 369 d) experiments were conducted at 298 K, with initial [Cs]0 and [Sr]0 concentrations from 10−5 to 10− mol kg−. Incongruent clay dissolution resulted in an accumulation of secondary aluminosilicate precipitates identified as nitrate-sodalite, nitrate-cancrinite and zeolite X, by molecular spectroscopy and electron microscopy (XRD, IR, NMR, SEM-EDS and TEM-EDS). Contaminant fate was dependent on competing uptake to parent clays and weathering products. TEM-EDS results indicated that high Il affinity for Cs was due to adsorption at frayed edge sites. The Il system also comprised Sr-rich aluminous precipitates after 369 d reaction time. In Mt systems, Cs and Sr were co-precipitated into increasingly recalcitrant spheroidal precipitates over the course of the experiment, whereas contaminant association with montmorillonite platelets was less prevalent. In contrast, Cs and Sr were found in association with weathered Vm particles despite the formation of spheroidal aluminosilicate precipitates that were comparable to those formed from Mt dissolution.  相似文献   

10.
Hydrochemical studies were carried out in Mulugu-Venkatapur Mandals of Warangal district, Telangana state, India to find out the causes of high fluorides in groundwater and surface water causing a widespread incidence of fluorosis in local population. The fluoride concentration in groundwater ranges from 0.28 to 5.48 mg/l with a mean of 1.26 mg/l in pre-monsoon and 0.21 to 4.43 mg/l with a mean 1.45 mg/l in post-monsoon. About 32% and 34% of samples in pre and post-monsoon containing fluoride concentrations that exceed the permissible limit. The Modified Piper diagram reflects that, water belong to Ca+2-Mg+2-HCO3 - to Na+-HCO3 - facies. Negative chloroalkali indices in both the seasons prove that ion exchange took place between Na+ & K+ with Ca+2 and Mg+2 in aquatic solution in host rock. Different plots for major ions and molar ratios suggest that weathering of silicate rocks and water-rock interaction is responsible for major ion chemistry of water. High fluoride content in groundwater attributed to continuous water-rock interaction during the process of percolation with fluorite bearing country rocks under arid, low precipitation, and high evaporation conditions. The low calcium content in rocks and soils, and the presence of high content of sodium bicarbonate in soils and waters are important factors favouring high levels of fluoride in waters. The basement rocks provide abundant mineral sources of fluoride in the form of amphibole, biotite, fluorite, mica and apatite.  相似文献   

11.
Uranium in Phosphorites   总被引：1，自引：0，他引：1  
The uranium concentration in phosphorites on continents and modern seafloor varies from 0.nto n· 102ppm (average 75 ppm). The average uranium concentration is 4–48 ppm in Precambrian and Cambrian deposits, 20–90 ppm in Paleozoic and Jurassic deposits, 40–130 ppm in Late Cretaceous–Paleogene deposits, 30–130 ppm in Neogene deposits, and 30–110 ppm in Quaternary (including Holocene) deposits. On the whole, the variation range is almost similar for phosphorites of different ages. The U/P2O5ratio in phosphorites ranges from less than unity to 24 · 10–4(average 3.2 · 10–4). Major phosphorite deposits of the world with ore reserves of approximately 250 Gt (or 58 Gt P2O5) contain up to 19 Mt of uranium. Uranium is present in phosphorites in the tetra- and hexavalent, i.e., U(IV) and U(VI) forms, and their ratio is highly variable. At the early diagenetic stage of the formation of marine phosphorites in a reductive environment, U(VI) diffuses from the near-bottom water into sediments. It is consequently reduced and precipitated as submicroscopic segregations of uranium minerals (mainly uraninite) that are probably absorbed by phosphatic material. During the subsequent reaction between phosphorites and aerated water and the weathering in a subaerial environment, uranium is partly oxidized and lost. The uranium depletion also occurs during catagenesis owing to a more complete crystallization of calcium phosphate and replacement of nonphosphatic components.  相似文献   

12.
The cereal soils of the Northwest of Tunisia derive most of the time, from alluvial deposits or altered remains of carbonated and clayey rocks. Extraction of the clayey fraction permitted to reveal the presence of the following clayey minerals: kaolinite, illite, smectite, chlorite, as well as an illite–smectite interstratified layer, which is present in the deep horizons of the vertisol and in the isohumic soil. The presence of such types of clays shows that the evolution mechanism of soils is weathering of primary minerals inherited from the sedimentary rocks of the Northwest of Tunisia. These clays ensure to soils most of their cationic exchange capacity. Thanks to these clays, which have Ca++, Mg++ and K+ as exchangeable cations, the chemical fertility of these soils is ensured. It may be improved by increasing contents of organic matter, which is naturally few abundant in these soils. To cite this article: H. Ben Hassine, C. R. Geoscience 338 (2006).  相似文献   

13.
[研究目的]非洲锰矿资源丰富,储量3.1亿t、资源量6.6亿t排名在世界上均列第一,加强非洲锰矿床的研究和认识对推动锰矿找矿工作具有重要的指导意义.[研究方法]通过对重要成矿带典型矿床的解剖总结了非洲锰矿床的成因类型、地质特征.[研究结果]非洲锰矿成因类型主要有前寒武系条带状铁建造(BIF)型、海相沉积型、陆相(三角洲...  相似文献   

14.
The Iberian type of volcano-sedimentary massive sulphide deposits   总被引：6，自引：0，他引：6  
The Iberian Pyrite Belt, located in the SW Iberian Peninsula, contains many Paleozoic giant and supergiant massive sulphide deposits, including the largest individual massive sulphide bodies on Earth. Total ore reserves exceed 1500 Mt, distributed in eight supergiant deposits (>100 Mt) and a number of other smaller deposits, commonly with associated stockwork mineralizations and footwall alteration haloes. Massive sulphide bodies largely consist of pyrite, with subordinated sphalerite, galena and chalcopyrite and many other minor phases, although substantial differences occur between individual deposits, both in mineral abundance and spatial distribution. These deposits are considered to be volcanogenic, roughly similar to volcanic-hosted massive sulphides (VHMS). However, our major conclusion is that the Iberian type of massive sulphides must be considered as a VHMS sub-type transitional to SHMS. This work is an assessment of the geological, geochemical and metallogenic data available up to date, including a number of new results. The following points are stressed; (a) ore deposits are located in three main geological sectors, with the southern one containing most of the giant and supergiant orebodies, whereas the northern one has mainly small to intermediate-sized deposits; (b) ore deposits differ one from another both in textures and mineral composition; (c) Co and Bi minerals are typical, especially in stockwork zones; (d) colloidal and other primary depositional textures are common in many localities; (e) a close relation has been found between ore deposits and some characteristic sedimentary horizons, such as black shales. In contrast, relationships between massive sulphides and cherts or jaspers remains unclear; (f) footwall hydrothermal alterations show a rough zoning, the inner alteration haloes being characterized in places by a high Co/Ni ratio, as well as by mobility of Zr, Y and REE; (g) 18O and D values indicate that fluids consist of modified seawater, whereas 34S data strongly suggest the participation of bacterial-reduced sulphur, at least during some stages of the massive sulphide genesis, and (h) lead isotopes suggest a single (or homogeneized) metal source, from both the volcanic piles and the underlying Devonian rocks (PQ Group). It is concluded that, although all these features can be compatible with classical VHMS interpretations, it is necessary to sketch a different model to account for the IPB characteristics. A new proposal is presented, based on an alternative association between massive sulphide deposits and volcanism. We consider that most of the IPB massive orebodies, in particular the giant and supergiant ones, were formed during pauses in volcanic activity, when hydrothermal activity was triggered by the ascent and emplacement of late basic magmas. In these conditions, deposits formed which had magmatic activity as the heat source; however, the depositional environment was not strictly volcanogenic, and many evolutionary stages could have occurred in conditions similar to those in sediment-hosted massive sulphides (SHMS). In addition, the greater thickness of the rock pile affected by hydrothermal circulation would account for the enormous size of many of the deposits. Received: 8 September 1998 / Accepted: 4 January 1999  相似文献   

15.
Photoabsorption by systems of hydrogen atoms and protons in the solar photosphere is studied. Analytical formulas for the partial cross sections for photodissociation of the H 2 + molecular ion are derived for the cases of fixed vibrational-rotational energy levels and averaging over a Boltzmann distribution for a given temperature. The photoabsorption coefficients for bound-free and free-free transitions of H-H+ in the solar photosphere are calculated. These are compared with the absorption coefficients for photo-ejection of an electron from a negative hydrogen ion H? and free-free transitions of an electron in the field of a hydrogen atom H. Results can be applied to the Sun and hotter stars.  相似文献   

16.
Exploration of Zn-rich sulphide deposits at Leadville, northern Lachlan Fold Belt, New South Wales, for over two decades has been largely on the premise that the mineralisation represents felsic volcanic-hosted massive sulphides (VHMS). Deposits are hosted by ?Silurian felsic metavolcanic, psammopelitic and calcareous metasedimentary rocks which have been intruded by the late Carboniferous I-type Gulgong Granite. Evidence for an epigenetic replacement (skarn) origin of the deposits, rather than representing metamorphosed volcanogenic massive sulphides, includes the proximity of evolved granitic intrusives and reactive carbonate rocks, a skarn mineral assemblage (with characteristic prograde and retrograde stages), lack of textural or lithological indications of an exhalative origin, and gossan and sulphide compositions consistent with Zn-Pb skarns and atypical of Lachlan Fold Belt VHMS deposits. Furthermore, sulphide lead isotope ratios are significantly more radiogenic than signatures for VHMS deposits in the Lachlan Fold Belt. Carbonate δ13C and δ18O and sulphide δ34S values are consistent with the interaction of magmatic hydrothermal fluids with Palaeozoic carbonate rocks and a largely magmatic source of sulphur. It is concluded that the Leadville deposits are of skarn type, genetically related to the Gulgong Granite.  相似文献   

17.
An anomalous Pb pattern occurs in drainage channel soils adjacent to the Elura Zn-Pb-Ag deposit and forms a fan shaped train extending at least 5 km on a mature weathering surface in semi-arid central-west New South Wales. This Pb pattern without a Zn component can be related to ferricrete fragments in the coarser fraction of the soil samples and has apparently formed as a result of mechanical dispersion of ferricrete from an earlier lateritic weathering profile. By considering residual Pb contents, after regressing for Fe content, the anomalous pattern can be extended and the contrast improved.  相似文献   

18.
There is an increasing interest in the distribution of rare earth elements (REEs) within soils, primarily as these elements can be used to identify pedogenetic processes and because soils may be future sources for REE extraction, despite much attention should be paid to the protection and preservation of present soils. Here, we evaluate the processes that control the distribution of REEs in subsoil horizons developed over differing lithologies in an area of low anthropogenic contamination, allowing estimates of the importance of source rocks and weathering. Specifically, this study presents new data on the distribution of REEs and other trace elements, including transition and high-field-strength elements, in subsoils developed on both Quaternary silica-undersaturated volcanic rocks and Pliocene siliciclastic sedimentary rocks within the Mt. Vulture area of the southern Apennines in Italy. The subsoils in the Mt. Vulture area formed during moderate weathering (as classified using the chemical index of alteration) and contain an assemblage of secondary minerals that is dominated by trioctahedral illite with minor vermiculite. The REEs, high-field-strength elements, and transition metals have higher abundances in subsoils that developed from volcanic rocks, and pedogenesis caused the Mt. Vulture subsoils to have REE concentrations that are an order of magnitude higher than typical values for the upper continental crust. This result indicates that the distribution of REEs in soils is a valuable tool for mineral exploration. A statistical analysis of inter-elemental relationships indicates that REEs are concentrated in clay-rich fractions that also contain significant amounts of low-solubility elements such as Zr and Th, regardless of the parent rock. This suggests that low-solubility refractory minerals, such as zircon, play a significant role in controlling the distribution of REEs in soils. The values of (La/Yb)N and (Gd/Yb)N fractionation indices are dependent on the intensity of pedogenesis; soils in the study area have values that are higher than typical upper continental crust ratios, suggesting that soils, especially those that formed during interaction with near neutral to acidic organic-rich surface waters, may represent an important source of both light REEs and medium REEs (MREEs). In comparison, MREE/heavy REE fractionation in soils that form during moderate weathering may be affected by variations in parent rock lithologies, primarily as MREE-hosting minerals, such as pyroxenes, may control (La/Sm)N index values. Eu anomalies are thought to be the most effective provenance index for sediments, although the anomalies within the soils studied here are not related to the alteration of primary minerals, including feldspars, to clay phases. In some cases, Eu/Eu* values may have a weak correlation with elements hosted by heavy minerals, such as Zr; this indicates that the influence of mechanical sorting of clastic particles during sedimentary transport on the Eu/Eu* values of siliciclastic sediments needs to be considered carefully.  相似文献   

19.
《Applied Geochemistry》1993,8(3):273-283
A new model for base cation release due to chemical weathering of soil minerals has been developed based on transition state theory, and included in the integrated soil chemistry model PROFILE. The data required for model application can be operationally determined on soil samples, making the model generally applicable and independent of any type of calibration. The model considers the contribution to the weathering rate from 12 groups of the most common primary and secondary minerals of soils, reacting in separate reactions with H+-ion, H2O, CO2 and organic acids expressed as dissolved organic carbon (DOC). The weathering rate sub-model couples the effects of dissolved Al and base cations on the reaction mechanisms. The model takes into account changes in soil temperature, different chemical conditions, the effect of vegetation interactions with the soil and N transformations. The kinetic coefficients and reaction orders are based on a complete re-evaluation of weathering data available in the literature, and additional kinetic data determined by the authors.Data from 23 different independent determinations of the field weathering rate from 15 sites in Scandinavia, Central Europe and North America were compiled and used to verify the model. The model is capable of estimating the release rate of base cations due to chemical weathering from information on soil mineralogy, texture and geochemical properties of the order of ±20% of the rate determined by independent methods. The results indicate that small amounts of dark minerals like epidote and hornblende, and the plagioclase content, largely determine the field weathering rate.  相似文献   

20.
Exchange reactions between Ca2+, H+ and Al species and their effects on the aluminium mobility in two Chinese acidic forest soils were studied. The study was based on a batch experiment using extractant solutions with different base cation (calcium) concentrations and pH. The experimental data showed that increased Ca2+ concentrations increased the release of soil hydrogen—and aluminium ions, especially from the more acid soil. In agreement with a cation exchange process, the treatment with Ca2+ extracts gave significantly decreased soil aluminium saturation (AlS) and increased calcium saturation (CaS) on the ion exchanger. Geochemical calculation using AlCHEMI program showed that activities of Al3+ in the extracts were all strongly under-saturated with respect to any gibbsite mineral in the studied pH region (i.e. below 4.1). There were instead apparently two different mechanisms controlling the activities of Al3+ in extracts. At pH between about 4.1 and 3.7, the Al3+ activity did not change significantly with pH. This is especially the case in the more acid soil. Apparently there are no sizeable pools available to release Al in this pH region. At pH below 3.7 (induced by higher Ca2+concentration) the activity of Al3+ increased with H+ though not in a pattern that complies with a gibbsite solubility control. An increase of base cation deposition would therefore mainly enhance the release of hydrogen ions between pH 4.1 and 3.7 and aluminium ions below pH 3.7 from Chinese mature acidic soils. This will cause an increased acidity of soil water in the short term and a decrease in the soil acidity in the long term. More attention should be paid to this fact in Chinese acid rain studies and control options.  相似文献   

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