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1.
The prevalence of sulphidic sediments in inland wetlands has been only recently recognized in many parts of the world, including Australia. The exposure of sulphidic sediments in these wetlands due to natural and human induced drying events has resulted in the oxidation of iron sulfide minerals, the formation of secondary iron minerals characteristic of acid sulfate soils and the release of highly acidic solutions. The objective of this study was to determine the mineralogy and morphology of sediments collected from the oxidized surface horizon (0-5 cm) of an inland acid sulfate soil located in south-western New South Wales (NSW), Australia. Random powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and scanning transmission electron microscopy combined with energy dispersive X-ray spectroscopy (STEM-EDS) techniques were used to characterize the minerals present in these sediments. Akaganéite was identified as the major mineral phase in the sediments; K-jarosite was also determined in small amounts in some sediments. The XRD patterns of sequentially washed (E-pure® water-0.01 M HCl-0.01 M EDTA) sediment samples showed all akaganéite peaks; the Rietveld refinement of these patterns also revealed a predominance of akaganéite. The chemical analyses of the original and washed sediments using STEM-EDS clearly showed the presence of akaganéite as a pure mineral phase with an average Fe/Cl mole ratio of 6.7 and a structural formula of Fe8O8(OH)6.8(Cl)1.2. These findings show that the extreme saline-acidic solutions (pH ∼ 2, EC = 216 dS/m) at the Bottle Bend lagoon provide ideal conditions for the crystallization of this rarely forming mineral. 相似文献
2.
探讨了人工合成的高价锰氧化物与紫外光(UV)联用时降解苯酚废水的特性。结果表明,氧化锰矿物在无UV时对苯酚的降解能力差异大,1 g/L的氧化锰4 h对200 mg/L苯酚废水的降解率和COD去除率分别为:锰钾矿97.51%、酸性水钠锰矿89.07%、碱性水钠锰矿11.36%、钙锰矿9.67%;锰钾矿87.79%、酸性水钠锰矿53.11%、碱性水钠锰矿6.42%、钙锰矿1.43%。UV光照下,氧化锰矿物对苯酚的降解率有不同程度的提高,且表现出显著的表面光催化性质,增加了苯酚的深度降解,COD去除率显著提高。UV下氧化锰4 h对苯酚的降解率分别为:锰钾矿99.48%、酸性水钠锰矿91.86%、碱性水钠锰矿40.15%、钙锰矿35.95%);COD的去除率分别为:锰钾矿98.11%、酸性水钠锰矿68.45%、钙锰矿27.57%、碱性水钠锰矿24.27%。MnO2-UV联用时降解苯酚可能包括两种主要作用机制:氧化锰矿物的直接化学氧化降解和UV下MnO2的表面光催化降解。 相似文献
3.
Résumé Les paragenèses résultant de l'enrichissement supergène de trois gisements manganésifères ouest-africains, d'origine précambrienne, diffèrent selon la nature des minéraux primaires. Elles ne diffèrent pas selon le contexte géographique et climatique actuel bien qu'il soit très varié.Cela confirme un enrichissement relativement ancien au cours d'une période humide concernant toute l'Afrique de l'Ouest.La transformation des protores des lentilles interstratifiées débute par l'apparition de minéraux transitoires: lithiophorite issue des grenats, manganite ou birnessite issues des carbonates et souvent relayées par la pyrolusite. Viennent ensuite des oxydes stables: cryptomélane, nsutite, ramsdellite. Cette dernière, bien représentée dans les minerais de cuirasses (formés par dépôt secondaire de manganèse dans certains sols), correspond au terme de l'évolution supergène. Aussi bien dans les lentilles que dans les cuirasses, la pyrolusite apparait instable.
The paragenesis resulting from supergene enrichment of three precambrian, west african, manganese deposits differ according to the nature of primary minerals. They do not differ with respect to present geographical and climatic environment in spite of their great diversity.The transformation of protores of the interstratified lenses commences with the appearance of transitory minerals: lithiophorite issued from garnets, manganite or birnesite issued from carbonates and often relayed by pyrolusite. Followed by stable oxides: cryptomelane, nsutite, ramsdelite. This last one is a major component of durricrust ores (formed by secondary precipitation of manganese in soils). It represents the final stage of supergene evolution. In interstratified lenses, as well as in durricrusts, pyrolusite appears instable.相似文献
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5.
随着我国钢铁工业和化学工业的迅猛发展,对锰矿资源的需求,日益增加.梅县锰矿公司对该县的锰矿地质和锰矿生产做了大量工作.在前人工作的基础上,我们在锰矿资源的调研中,曾对广东省梅县的宝山岗、白沙坪、桃尧大华、宝坑、仙水塘、磔角坑、车陂等地的锰矿体、进行过采样工作.经室内鉴定后、梅县的锰矿石有优质的放电锰矿石和冶金用锰矿石、矿床规模属于中小型.梅县锰矿资源的生产,继续已有20多年的历史,在矿床的质和量方面尚需做更深入的研究,以便为矿山开采和锰矿生产提供更充分的依据.本文是对锰矿物质成分初步研究的部分结果. 相似文献
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Manganese ores of Nishikhal occur as distinctly conformable bands in the khondalite suite of rocks belonging to the Precambrian
Eastern Ghats complex of south Orissa, India. Manganese minerals recorded are cryptomelane, romanechite, pyrolusite, with
minor amounts of jacobsite, hausmannite, braunite, lithiophorite, birnessite and pyrophanite. Goethite, graphite, hematite
and magnetite are the other opaque minerals and quartz, orthoclase, garnet, kaolinite, apatite, collophane, fibrolite, zircon,
biotite and muscovite are the gangue minerals associated with these ores. The mineral chemistry of some of the phases, as
well as the modes of association of phosphorous in these ores have been established. The occurrence of well-defined bands
of manganese ore; co-folding of manganese ore bands and associated metasedimentary country rocks; the min-eral assemblage
of spessartite-sillimanite-braunite-jacobsite-hausmannite; the geochemical association of Mn-Ba-Co-Ni-Zn together with the
Si versus Al and Na versus Mg plots of the manganese ores suggest that the Nishikhal deposit is a metamorphosed Precambrian
lacustrine deposit. Continental weathering appears to be the source for manganese and iron. After deposition and probable
diagenesis, the manganese-rich sediments were metamorphosed along with conformable psammitic and pelitic sediments under granulite
facies conditions, and subsequently underwent supergene enrichment to produce the present deposit.
Received: 14 March 1995 / Accepted: 11 April 1996 相似文献
8.
Chemical, thermal, X Ray analysis, and microscopic observation of romanechites, cryptomelanes, and coronadites indicate some specific features for each of these oxide.Structural calculation shows a theoretical ratio Ba/H2O close to 12 for romanechite, slightly different for samples from cuirass. In the group cryptomelane, coronadite, hollandite the ratio: (Ba, K, Pb)/H2O equals generaly 11, exceptionnally 12 under supergene conditions.Thermogravimetric curves indicate some weight loss starting at low temperature for romanechite and cryptomelane and higher temperature for coronadite and hollandite.Optical properties of these oxides seem to be more influenced by the evolution of the ore complex than by their own chemical particularities.The microscopic anisotropy is higher for romanechite and coronadite than for cryptomelane.Romanechite, cryptomelane, and coronadite present a great stability under surface conditions, where these oxides generally replace pyrolusite. 相似文献
9.
David M. Sherman 《Geochimica et cosmochimica acta》2005,69(13):3249-3255
Sunlight-induced reduction and dissolution of colloidal Fe-Mn (hydr)oxide minerals yields elevated concentrations of Fe2+ and Mn2+ in natural waters. Since these elements may be biolimiting micronutrients, photochemical reactions might play a significant role in biogeochemical cycles. Reductive photodissolution of Fe (hydr)oxide minerals may also release sorbed metals. The reactivity of Fe-Mn (hydr)oxide minerals to sunlight-induced photochemical dissolution is determined by the electronic structure of the mineral-water interface. In this work, oxygen K-edge absorption and emission spectra were used to determine the electronic structures of iron(III) (hydr)oxides (hematite, goethite, lepidocrocite, akaganeite and schwertmannite) and manganese(IV) oxides (pyrolusite, birnessite, cryptomelane). The band gaps in the iron(III) (hydr)oxide minerals are near 2.0-2.5 eV; the band gaps in the manganese (IV) oxide phases are 1.0-1.8 eV. Using published values for the electrochemical flat-band potential for hematite together with experimental pHpzc values for the (hydr)oxides, it is possible to predict the electrochemical potentials of the conduction and valence bands in aqueous solutions as a function of pH. The band potentials enable semiquantitative predictions of the susceptibilities of these minerals to photochemical dissolution in aqueous solutions. At pH 2 (e.g., acid-mine waters), photoreduction of iron(III) (hydr)oxides could yield millimolal concentrations of aqueous Fe2+ (assuming surface detachment of Fe2+ is not rate limiting). In seawater (pH 8.3), however, the direct photo-reduction of colloidal iron(III) (hydr)oxides to give nanomolal concentrations of dissolved, uncomplexed, Fe2+ is not thermodynamically feasible. This supports the hypothesis that the apparent photodissolution of iron(III) (hydr)oxides in marines systems results from Fe3+ reduction by photochemically produced superoxide. In contrast, the direct photoreduction of manganese oxides should be energetically feasible at pH 2 and 8.3. 相似文献
10.
Sorption and desorption of dissolved organic phosphorus onto iron (oxyhydr)oxides in seawater 总被引：2，自引：0，他引：2
Sorption of phosphorus (P) onto particulate surfaces significantly influences dissolved P concentrations in aquatic environments. We present results of a study contrasting the sorption behavior of several dissolved organic phosphorus (DOP) compounds and phosphate onto three commonly occurring iron (oxyhydr)oxides (Feox): ferrihydrite, goethite, and hematite. The DOP compounds were chosen to represent a range of molecular weights and structures, and include: adenosine triphosphate (ATP), adenosine monophosphate (AMP), glucose-6-phosphate (G6P), and aminoethylphosphonic acid (AEP).All P compounds displayed decreasing sorption as a function of crystallinity of the Feox substrate, with ferrihydrite adsorbing the most, hematite the least. In general, maximum sorption density decreased with increasing molecular weight of P compound; sorption of G6P onto goethite and hematite excepted. P compound size and structure, and the nature of the Feox substrate all appear to play a role dictating relative sorption capacity. Failure of a simple, 1-step sorption-desorption model to describe the data suggests that P sorption cannot be explained by a simple balance between sorption and desorption. Instead, the data are consistent with a 2-step sorption model consisting of an initial rapid surface sorption, followed by a slow, solid-state diffusion of P from surface sites into particle interiors. Desorption experiments provide additional support for the 2-step sorption model.Without exception, DOP compounds showed less efficient sorption than did orthophosphate. This suggests that in aquatic systems enriched in reactive Feox, whether as suspended particulates in the water column or in benthic sediments, DOP bioavailability may exceed that of orthophosphate. Since biological uptake of P from DOP requires enzymatic cleavage of orthophosphate, a system enriched in DOP relative to orthophosphate may impact ecosystem community structure. 相似文献
11.
Conditional surface binding constants and complexation capacities for Zn, Pb, Cd, and Cu were determined from surface titration experiments of heterogeneous natural aquatic particulate matter of different origin and composition. Metals and particles were evaluated in naturally occurring concentration ranges in river water.The adsorption of trace metals can be adequately described with a single conditional binding constant over a wide range of metal : particle ratios. Binding constants for aquatic particles at pH 8.0 are remarkably independent from particle composition and are specific for each metal: log Kads
Zn = 8.39, log Kads
Pb = 9.67, log Kads
Cd = 8.61, log ads
Cu = 9.84. From competition experiments with Ca and Pb we extracted a sorption coefficient for Ca of log Kads
Ca = 2.5 (pH 8.0). Maximum surface binding capacities for all metal ions were found for particles containing high fractions of Mn-oxides which are associated with large specific surface areas. Generally, we found sorption capacities to decrease in the sequence Cu Pb, Zn > Cd.The experiments suggest that the conditional surface binding constants and complexation capacities are applicable to model trace metal adsorption in the concentration ranges of natural waters under conditions similar to the experiments. Results also imply that the chemical nature of particle surface sites is rather uniform in the intermediate concentration range or that the array of binding sites averages out differences in sorption strength over the prevailing concentration range of metal ions, respectively. 相似文献
12.
红土型风化壳和次生锰矿床形成于温暖和潮湿的古气候条件 ,其中含有丰富的表生钾锰矿物。因此 ,对表生钾锰矿物进行精确的40 Ar/ 3 9Ar年龄测定 ,不仅能查明大陆化学风化和矿床次生富集的时间和过程 ,而且可以为区域古气候的反演提供重要的年代学资料。透射电子显微镜、热重分析、离子交换实验和40 Ar/ 3 9Ar同位素分析表明 ,层状结构的黑锌锰矿、锂锰矿和钠水锰矿以及具有 1× 1隧道结构的软锰矿不适合于40 Ar/ 3 9Ar年龄测定 ;而隐钾锰矿、锰钡矿和锰铅矿因具有致密和稳定的 2× 2隧道结构及很强的保存K Ar体系的能力 ,是40 Ar/ 3 9Ar同位素定年的理想对象。硬锰矿和钙锰矿分别具有 2× 3和 3× 3隧道结构 ,由于隧道孔径过大 ,晶体结构的稳定性较差 ,其作为40Ar/ 3 9Ar测年的适用性有待于进一步证实。采用精细的激光阶段加热技术 ,可以有效克服表生钾锰矿物40 Ar/ 3 9Ar测年过程中3 9ArK 的反冲损失、多世代表生钾锰矿物的共生 ,以及表生钾锰矿物中原生矿物的污染和过量大气氩的存在等问题 ,并获得有意义的风化年龄。已有数据表明 ,表生钾锰矿物的形成主要集中在白垩纪末期、始新世末期—渐新世早期、中新世和上新世中期等 4个时期 ,可能记录了地史时期周期性的化学风化及气候的交替演变 相似文献
13.
Roger G Burns 《Geochimica et cosmochimica acta》1976,40(1):95-102
Strong enrichments of cobalt occur in marine manganese nodules, soils, wads, and natural and synthetic minerals such as hollandite, cryptomelane, psilomelane, lithiophorite, birnessite, and δ-MnO2. Previously, it was suggested that Co3+ ions in these minerals replace either Mn3+ or substitute for Fe3+ in incipient goethite epitaxially intergrown with δ-MnO2. Neither of these interpretations is now considered to be satisfactory on account of the large discrepancy of ionic radius between octahedrally coordinated low-spin Co3+ and high-spin Mn3+ or Fe3+ in oxide structures. The close agreement between the ionic radii of Co3+ and Mn4+ suggests that some cobalt substitutes for Mn4+ ions in edge-shared [MnO6] octahedra in many manganese(IV) oxide mineral structures. It is proposed that hydrated cations, including Co2+ ions, are initially adsorbed on to the surfaces of certain Mn(IV) oxides in the vicinity of essential vacancies found in the chains or sheets of edge-shared [MnO6] octahedra. Subsequently, fixation of cobalt takes place as a result of oxidation of adsorbed Co2+ ions by Mn4+ and replacement of the displaced manganese by low-spin Co3+ ions in the [MnO6] octahedra or vacancies. 相似文献
14.
Résumé Des encroûtements de bioxyde de manganèse d'une épaisseur de quelques millimètres recouvrent les rochers granitiques de l'Anse de Belmont (Loire-Atlantique, France). Ils sont découverts à marée basse. Ils sont constitués de bioxyde hydraté amorphe, todorokite, ranciéite et cryptomélane qui sont agencés selon l'édifice des micas. Leur teneur en fer est très faible; ils sont enrichis en cobalt et uranium. Des eaux douces riches en manganèse et pauvres en fer se jettent dans la mer au niveau de ces dépôts qui se forment par réaction de précipitation du manganèse au moment du mélange des eaux douces avec l'eau de mer. Les observations sur place indiquent que ces dépôts sont récents, et que leur croissance est rapide.Manganese dioxide concretions, a few millimeters thick, are covering granite outcrops in the intertidal area of the cove of Belmont (Loire-Atlantique, France). The concretions are constituted by an association of several manganese dioxide minerals (amorphous hydrated dioxide, todorokite, ranciéite and cryptomelane) which are epitaxially growing on the mica minerals of the granite. The concretions have a very low iron content, and are enriched in cobalt and uranium. A fresh water spring, with high manganese and low iron concentration, is flowing out at the level of the MnO2 concentrations. The mixing of sea water and fresh waters leads to MnO2 precipitation. Field observations show that the concretions are recent and that they grow rapidly. 相似文献
15.
S. L. S. Stipp M. Hansen R. Kristensen M. F. Hochella Jr. L. Bennedsen K. Dideriksen T. Balic-Zunic D. Lonard H. -J. Mathieu 《Chemical Geology》2002,190(1-4):321-337
The behaviour of Fe-oxides was investigated during precipitation and co-precipitation, phase transformation and dissolution, while their ability to adsorb and incorporate trace components was examined. Some samples were synthesised and studied under controlled laboratory conditions and other samples were taken from experiments designed to test the effectiveness of waste treatment strategies using iron. Surface-sensitive and high-resolution techniques were used to complement information gathered from classical, macroscopic methods.
Adsorption isotherms for Ni2+ uptake on synthetic ferrihydrite (Fe5HO8·4H2O, often written simply Fe(OH)3), goethite (-FeOOH), hematite (-Fe2O3) and magnetite (Fe3O4) were all similar, increasing as expected at higher pH. Desorption behaviour was also similar, but one third or more of the Ni2+ failed to return to solution. In the past, “irreversible sorption” has been blamed on uptake into micro-fractures or pores, but during examination (using Atomic force microscopy, AFM) of hundreds of Fe-oxide particles, no evidence for such features could be found, leading to the conclusion that Ni2+ must become incorporated onto or into the solids. When solutions of Fe(II) are oxidised in controlled laboratory conditions or during treatment of ash from municipal waste incinerators, two-line ferrihydrite forms rapidly and on never-dried samples, AFM shows abundant individual particles with diameter ranging from 0.5 to several tens of nanometers. Aging in solution at 70°C promotes growth of the particles into hematite and goethite and their identification (by X-ray powder diffraction, XRPD, with Rietveld refinement) becomes possible at the same aging stage as mineral morphology becomes recognisable by AFM. In other experiments that were designed to mimic natural attack by organic acids, colloidal lepidocrocite (γ-FeOOH) was observed in situ by AFM, while reductive dissolution removed material on specific crystal faces. Lath ends are eroded fastest while basal planes are more stable.
In order to help elucidate mechanisms of contaminant immobilisation by Fe-oxides, we examined samples from a reactive barrier made with 90% quartz sand, 5% bentonite and 5% zero-valent iron filings that had reacted with a solution typical of leachate from coal-burning fly ash using time-of-flight secondary ion mass spectroscopy (TOF-SIMS). Fe(0) oxidised to Fe(III), while soluble and toxic Cr(VI) was reduced to insoluble Cr(III). Chemical maps show Fe-oxide coatings on bentonite; Cr is associated with Fe-oxides to some extent but its association with Ca in a previously undescribed phase is much stronger. Other samples taken from municipal waste incinerator ash that had been treated by aeration in Fe(II) solutions were examined with transmission electron microscopy (TEM), selected area electron diffraction (SAED) and energy dispersive X-ray spectroscopy (EDS). Pb and some Zn are seen to be dispersed throughout two-line ferrihydrite aggregates, whereas Sn and some Zn are incorporated simply as a result of entrainment of individual ZnSn-oxide crystallites.
Geochemical speciation models that fail to account for contaminant uptake in solid solutions within major phases or as thin coatings or entrained crystals of uncommon phases such as those described here risk to underestimate contaminant retardation or immobilisation. 相似文献
16.
Sorption of U(VI) on Hanford fine sand (HFS) with varying Fe-oxide (especially ferrihydrite) contents showed that U(VI) sorption increased with the incremental addition of synthetic ferrihydrite into HFS, consistent with ferrihydrite being one of the most reactive U(VI) sorbents present in natural sediments. Surface complexation model (SCM) calculations for U(VI) sorption, using only U(VI) surface-reaction constants obtained from U(VI) sorption data on freshly synthesized ferrihydrite at different pHs, were similar to the measured U(VI) sorption results on pure synthetic ferrihydrite and on HFS with high contents of ferrihydrite (5 wt%) added. However, the SCM prediction using only U(VI) sorption reactions and constants for synthetic ferrihydrite overestimated U(VI) sorption on the natural HFS or HFS with addition of low amounts of added ferrihydrite (1 wt% added). Over-predicted U(VI) sorption was attributed to reduced reactivity of natural ferrihydrite present in Hanford Site sediments, compared to freshly prepared synthetic ferrihydrite. Even though the SCM general composite (GC) approach is considered to be a semi-quantitative estimation technique for contaminant sorption, which requires systematic experimental data on the sorbent–sorbate system being studied to obtain credible SCM parameters, the general composite SCM model was still found to be a useful technique for describing U(VI) sorption on natural sediments. Based on U(VI) batch sorption results, two simple U(VI) monodentate surface species, SO_UO2HCO3 and SO_UO2OH on ferrihydrite and phyllosillicate in HFS, respectively, can be successfully used to describe U(VI) sorption onto Hanford Site sediment contacting varying geochemical solutions. 相似文献
17.
A study of the pattern of dissolution of synthetic and natural Fe oxides in 6 M HCl indicates that the rate of element release from synthetic Fe oxides is strongly influenced by mineralogy and the level of element incorporation. Synthetic maghemite (γ-Fe2O3) samples are subject to much more rapid dissolution than goethite (FeOOH) and hematite (α-Fe2O3). In samples dominated by hematite and maghemite, Cu, Zn and particularly Pb, in comparison to Fe, are preferentially released during the early stages of dissolution. Similar patterns are apparent from the dissolution of hematite- and maghemite-dominated samples derived from natural gossan. Comparison of XRD scans with data from the dissolution of natural gossan samples transformed by incremental heating to hematite- and maghemite-dominated assemblages suggests that the degree of crystallinity may also be a significant factor in the release of elements incorporated in the Fe oxides. Ferruginous materials made up of varying proportions of goethite, hematite, maghemite, kaolinite and quartz are important sampling materials in a range of regolith environments. These are products of complex chemical and mechanical mobilization over long periods of geological time. If the patterns of Fe oxide dissolution in 6 M HCl and the release of incorporated metals reflect stability in such weathering regimes, knowledge of the retention characteristics of incorporated metals in different Fe oxide phases, as indicated by this study, will be useful in the planning and interpretation of geochemical surveys in such regions. 相似文献
18.
Mario Villalobos Brandy Toner Garrison Sposito 《Geochimica et cosmochimica acta》2003,67(14):2649-2662
Manganese oxides form typically in natural aqueous environments via Mn(II) oxidation catalyzed by microorganisms, primarily bacteria, but little is known about the structure of the incipient solid-phase products. The Mn oxide produced by a Pseudomonas species representative of soils and freshwaters was characterized as to composition, average Mn oxidation number, and N2 specific surface area. Electron microscopy, X-ray diffraction, and X-ray absorption near edge structure spectroscopy were applied to complement the physicochemical data with morphological and structural information. A series of synthetic Mn oxides also was analyzed by the same methods to gain better comparative understanding of the structure of the biogenic oxide. The latter was found to be a poorly crystalline layer type Mn(IV) oxide with hexagonal symmetry, significant negative structural charge arising from cation vacancies, and a relatively small number of randomly stacked octahedral sheets per particle. Its properties were comparable to those of δ-MnO2 (vernadite) and a poorly crystalline hexagonal birnessite (“acid birnessite”) synthesized by reduction of permanganate with HCl, but they were very different from those of crystalline triclinic birnessite. Overall, the structure and composition of the Mn oxide produced by P. putida were similar to what has been reported for other freshly precipitated Mn oxides in natural weathering environments, yielding further support to the predominance of biological oxidation as the pathway for Mn oxide formation. Despite variations in the degree of sheet stacking and Mn(III) content, all poorly crystalline oxides studied showed hexagonal symmetry. Thus, there is a need to distinguish layer type Mn oxides with structures similar to those of natural birnessites from the synthetic triclinic variety. We propose designating the unit cell symmetry as an addition to the current nomenclature for these minerals. 相似文献
19.
S EmmanuelY Erel 《Geochimica et cosmochimica acta》2002,66(14):2517-2527
Lead concentrations and stable isotopic measurements were examined in the different chemical fractions of Czech forest soils to investigate the mechanisms of Pb partitioning. A method of selective sequential dissolution (SSD) was employed that distinguished between five different fractions: exchangeable, surface bound, organic matter, Fe-oxides, and silicates (non-labile).From an analysis of the concentrations and isotopic compositions associated with the different fractions, it is apparent that Pb in the deep Czech mineral soils is of predominantly natural origin and is primarily associated with silicates (69-81%) and Fe-oxides (11-19%). Natural Pb associated with surface bound and organic matter fractions in mineral soils accounts for only 7 to 15%. Anthropogenic Pb in the Czech soils is concentrated primarily in the organic horizons and is strongly associated with the surface-bound and organic matter fractions in which the proportion of total Pb is 33 to 50% and 23 to 47%, respectively.At high and low levels of contamination, Pb isotopic signatures within the labile fractions of the same soil samples are generally homogenous, although a degree of heterogeneity among these fractions is noted in samples of intermediate degrees of contamination. Such heterogeneity probably reflects different levels of natural and anthropogenic Pb mixing.Determination of the mass-normalized affinity of Pb to the primary components using solid-solution distribution coefficients suggests that in Czech forest soils, the order of affinity may be summarized as Fe-oxides > organic matter > silicates. A similar treatment of the data reported for semiarid Mediterranean soils indicates the prevailing order to be Fe-oxides > carbonates > organic matter > silicates. The general similarity of the behaviour of Pb with respect to the different soil components in both temperate and semiarid soils suggests that these orders of affinity may have wider significance for a variety of other soil types. 相似文献