Anthropogenic Pt and Pd concentrations in urban roadside soils from Xuzhou, China

The increased use of platinum group elements (PGE) as automobile catalysts has led to concern over potential environmental and biological accumulation. These inputs are greatest in urban areas, with the major sinks being roadside soils. This investigation…     

Trace elements distribution and mineralogical composition in the < 2-μm size fraction of shales from the Southern Apennines,Italy

Summary Mineralogical composition and trace elements distribution in the < 2-m size fraction of Late Cretaceous-Oligocene shales from the Southern Apennines (Italy) are presented.The clay mineral assemblage consists of illite, smectite, kaolinite and minor chlorite. Analytical evidence points to a detrital micaceous precursor for illite and smectite. Accessory phases were also found. Chemical data, normalized with respect to the Post-Archean Australian Shales (PAAS), indicate depletion of Ba, Rb, Y, Zr and enrichment of Nb. PAAS-normalized REE-patterns exhibit a positive Eu anomaly and HREE depletion. A kaolinite-rich sample has high REE contents in contrast to smectite-rich fractions. A REE-pattern without appreciable Eu anomaly is displayed by the illite-rich sample.Statistical data processing indicates a link between Ti, P, Y, Zr, Nb and Yb, suggesting that accessory phases may play a role in controlling HREE and that the observed LREE/HREE fractionation may also be due to hydraulic sorting of these phases. An important La-kaolinite relationship accounts for the capability of this phase to host LREE. Smectite and, thus, adsorption mechanisms, appear to exert a limited role in distributing REE. The Eu anomaly is a source inherited feature, probably not determined solely by clay minerals.

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Spurenelement-Verteilung und mineralogische Zusammensetzung der < 2m Fraktion von Schiefern aus dem südlichen Appenin (Italien)

Zusammenfassung Die mineralogische Zusammensetzung und die Verteilung der Spurenelemente in der < 2 m Fraktion von spät-kretazischen-oligozänen Schiefern aus dem südlichen Appenin (Italien) werden in Übersicht gebracht. Die Tonmineral-Vergesellschaftung besteht aus Illit, Smectit, Kaolinit und kleineren Mengen von Chlorit. Analytische Daten weisen darauf hin, daß Illit und Smectit aus einem detritischen Glimmermineral hervorgegangen sein dürften. Auch akzessorische Phasen kommen vor. Chemische Daten zeigen gegenüber post-Archaischen australischen Schiefern (PAAS) eine Verarmung in Ba, Rb, Y, Zr und eine Anreicherung von Nb. PAAS-normalisierte SEE-Verteilungsmuster zeigen eine positive Eu Anomalie und eine Verarmung an HSEE. Eine Kaolinit-reiche Probe zeigt hohe Gehalte an gesamten SEE im Gegensatz zu einer Smectit-reichen. Die Illit-reiche Probe zeigt ein SEE-Verteilungsmuster ohne deutliche Eu Anomalie.Statistische Verarbeitung der Daten läßt eine Verbindung zwischen Ti, P, Y, Zr, Nb und Yb erkennen; dies weist darauf hin, daß akzessorische Phasen einen Einfluß auf die HSEE-Verteilung haben und daß die beobachtete LSEE/HSEE Fraktionierung auch auf hydraulische Sortierung dieser Phasen zurückgehen könnte. Es gibt eine bedeutsame Beziehung zwischen La und Kaolinit und diese unterstreicht die Fähigkeit des Kaolinits für die Aufnahme von LSEE. Smectit und Adsorptionsmechanismen scheinen eine geringe Rolle für die Verteilung der SEE zu spielen. Die Eu Anomalie ist eine Erscheinung, die auf die Quelle der sedimentären Minerale zurückgeht und wahrscheinlich nicht ausschließlich durch Tonminerale bestimmt wird.

     

Determination of geochemical background for environmental studies of soils via the use of HNO<Subscript>3</Subscript> extraction and Q–Q plots

The procedure proposed in this study is based on the extraction of elements in soils by analytical grade HNO₃, the distribution of the elemental data displayed on probability graphs (Q–Q plots) and the visualization of the results spatially by GIS software. The applicability of the procedure is demonstrated in an urban area and its surroundings (Kavala, northern Greece). A major (Ca) and a trace (Ag) element are used as examples in order to demonstrate the applicability of the proposed procedure. Normal probability and lognormal probability plots of Ca and Ag show that their concentrations are lognormally distributed and that their geochemical baseline and anomaly threshold values can be calculated with the aid of their geometric mean and geometric deviation. The advantages of the proposed procedure are simplicity, comprehensiveness, and low cost. It can be applied to environmental geochemical studies of soils in a variety of areas.     

Spatio-temporal variations of δ<Superscript>2</Superscript>H and δ<Superscript>18</Superscript>O in precipitation and shallow groundwater in the Hilly Loess Region of the Loess Plateau,China

Groundwater is of utmost significance to socio-economic development and ecological recovery for the Loess Plateau. However, studies regarding the mechanism governing groundwater recharge over this area appear to be inadequate. This study is to examine the spatio-temporal variations of δ²H and δ¹⁸O in precipitation and shallow groundwater. On the basis of this, the mechanisms governing shallow groundwater recharge were explored. Precipitation and groundwater were sampled monthly from May to October during the period 2004–2006 at 13 sites in the Chabagou Catchment (187 km²). In the Caopingxigou Experimental Watershed (0.1 km²), meteorological variables were observed and rainfall larger than 5 mm was sampled immediately after each rain event. Across the area, 90% of the precipitation occurred from May to September primarily in the form of heavy rains or rainstorms with great spatial variability. There were about 30 localized rains in each year. It was indicated that there existed notable seasonality and pronounced spatial variability in precipitation isotopic compositions. Contributing factors and indications of isotopic compositions, as well as their climatic indications such as monsoon intensities and mixing processes of water vapor, were investigated. The δ²H–δ¹⁸O relation of groundwater was found to be δ²H = 3.22 × δ¹⁸O − 38.1, deviating from the local meteoric water line δ²H = 7.57 × δ¹⁸O + 3.9. The range of δ values in groundwater is shrunken to be 15–21% of that in individual precipitations, and groundwater in the middle reaches shows a wider range of δ values. Isotopic results showed that groundwater originates from precipitation with hydrogen and oxygen isotopic compositions being −69 and −9.7‰, respectively, and most groundwater experiences serious evaporation and adequate mixing with old water during infiltration or percolation in the aerated zone. It was also founded that obvious fluctuations of isotopic compositions in groundwater mainly appear in the middle reaches especially at sites that are close to valleys, suggesting varying sources of groundwater from precipitation, precipitation runoff, isotopically enriched surface water and/or lateral recharge of adjacent groundwater.     

Fe(II) reduction of pyrolusite (β-MnO<Subscript>2</Subscript>) and secondary mineral evolution

Iron (Fe) and manganese (Mn) are the two most common redox-active elements in the Earth’s crust and are well known to influence mineral formation and dissolution, trace metal sequestration, and contaminant transformations in soils and sediments. Here, we characterized the reaction of aqueous Fe(II) with pyrolusite (β-MnO₂) using electron microscopy, X-ray diffraction, aqueous Fe and Mn analyses, and ⁵⁷Fe Mössbauer spectroscopy. We reacted pyrolusite solids repeatedly with 3 mM Fe(II) at pH 7.5 to evaluate whether electron transfer occurs and to track the evolving reactivity of the Mn/Fe solids. We used Fe isotopes (56 and 57) in conjunction with ⁵⁷Fe Mössbauer spectroscopy to isolate oxidation of Fe(II) by Fe(III) precipitates or pyrolusite. Using these complementary techniques, we determined that Fe(II) is initially oxidized by pyrolusite and that lepidocrocite is the dominant Fe oxidation product. Additional Fe(II) exposures result in an increasing proportion of magnetite on the pyrolusite surface. Over a series of nine 3 mM Fe(II) additions, Fe(II) continued to be oxidized by the Mn/Fe particles suggesting that Mn/Fe phases are not fully passivated and remain redox active even after extensive surface coverage by Fe(III) oxides. Interestingly, the initial Fe(III) oxide precipitates became further reduced as Fe(II) was added and additional Mn was released into solution suggesting that both the Fe oxide coating and underlying Mn phase continue to participate in redox reactions when freshly exposed to Fe(II). Our findings indicate that Fe and Mn chemistry is influenced by sustained reactions of Fe(II) with Mn/Fe oxides.

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Geochemistry of isotopes (δ<Superscript>13</Superscript>C and δ<Superscript>18</Superscript>O) and depositional environment of the upper Kazanian carbonate sediments in the Volga-Vyatka interfluve

This work reports the results of lithological and isotopic study of carbonate rocks from the Pechishchi stratotype section (Kazan) and three adjacent sections of Kazanian rocks of the Volga-Vyatka region at the eastern Russian Platform. These sections were recovered by the Kremeshki, Popovtsevo, and Chimbulat quarries (near the town of Sovetsk, southeastern Kirov district). Lithological features and wide variations of δ¹³C (from −6.0 to 6.8‰) and δ¹⁸ O (from 22.9 to 33.4 ‰) indicate that the rocks were formed in a shallow-marine basin with rapidly varying conditions of sedimentation which characterize different facies (and/or paleoecological) zones: lagoonal, supralittoral, littoral, shoal. They also suggest processes of postsedimentary alteration (mainly, under supergene conditions). Numerous short-term hiatuses are also recorded.     

Assessment of NO<Subscript>3</Subscript><Superscript>−</Superscript> contamination in a karstic aquifer,with the use of geochemical data and spatial analysis

Kopaida plain is a cultivated region of Eastern Greece, with specific characteristic related with the paleogeographic evolution and the changes in land use. The present article examines the contamination that derives from nitrates, in terms of contaminant levels, definition of sources and spatial distribution of contaminant plume. For this purpose, 50 water samples were collected from the karstic aquifer and analyzed for 15 parameters including major ions, trace elements, physicochemical parameters, and stable isotopes. The assessment of the above parameter values along with the notes derived by the statistical process revealed the existence of nitrate contamination which has been spatial defined with the aid of spatial interpolation techniques. The correlation of NO₃ ⁻ concentrations with the stable isotope values, defined the infiltration conditions and showed contaminant transport. Nitrate values revealed the potential environmental threat for local people, as 10% of the samples exceeded the parametric value of 50 ppm and 54% of them are above 25 ppm, indicating no optimal quality conditions. The origin of nitrate contamination seems to derive exclusively from the application of N-fertilizers, since the rest of potential sources were not verified by analytical data and field works.     

Paleozoic tectonics of the southern Chinese Tianshan: Insights from structural,chronological and geochemical studies of the Heiyingshan ophiolitic mélange (NW China)

In the southern Chinese Tianshan, the southernmost part of the Central Asian Orogenic Belt (CAOB), widespread ophiolitic mélanges form distinct tectonic units that are crucial for understanding the formation of the CAOB. However, the timing of tectonic events and the subduction polarity are still in controversy. In order to better understand these geological problems, a comprehensive study was conducted on the Heiyingshan ophiolitic mélange in the SW Chinese Tianshan. Detailed structural analysis reveals that the ophiolitic mélange is tectonically underlain by sheared and weakly metamorphosed pre-Middle Devonian rocks, and unconformably overlain by non-metamorphic and undeformed lower Carboniferous (Serpukhovian) to Permian strata. The igneous assemblage of the mélange comprises OIB-like alkali basalt and andesite, N-MORB-like tholeiitic basalt, sheeted diabase dikes, cumulate gabbro and peridotite. Mafic rocks display supra-subduction signatures, and some bear evidence of contamination with the continental crust, suggesting a continental marginal (back-arc) basin setting. Zircons of a gabbro were dated at 392 ± 5 Ma by the U–Pb LA-ICP-MS method. Famennian–Visean radiolarian microfossils were found in the siliceous matrix of the ophiolitic mélange. Mylonitic phyllite which displays northward-directed kinematic evidence yielded muscovite ⁴⁰Ar/³⁹Ar plateau ages of 359 ± 2 Ma and 356 ± 2 Ma.These new data, combined with previously published results, suggest that the mafic protoliths originally formed in a back-arc basin in the Chinese southern Tianshan during the late Silurian to Middle Devonian and were subsequently incorporated into the ophiolitic mélange and thrust northward during the Late Devonian to early Carboniferous. Opening of the back-arc basin was probably induced by south-dipping subduction of the Paleo-Tianshan Ocean in the early Paleozoic, and the Central Tianshan block was rifted away from the Tarim block. Closure of the back-arc basin in the early Carboniferous formed the South Tianshan Suture Zone and re-amalgamated the two blocks.     

Isotope (δ<Superscript>13</Superscript>C and δ<Superscript>18</Superscript>O) and genetic features of manganese carbonates of the Mazul deposit (Krasnoyarsk region)

New isotope and mineral data on manganese carbonates of the Mazul deposit (Krasnoyarsk region) in combination with morphology of ore bodies suggest that the ores were formed in several stages with the involvement of meteoric solutions through infiltration and, possibly, exfiltration mechanisms. Based on the geological–geochemical data, manganese carbonates of the Mazul deposit may be ascribed to a new genetic subtype of the catagenesis (epigenesis) zone.     

Mineralogical and geochemical characterization of the Riópar non-sulfide Zn-(Fe-Pb) deposits (Prebetic Zone,SE Spain)

The present paper reports the first detailed petrological and geochemical study of non-sulfide Zn–(FePb) deposits in the Riópar area (Prebetic Zone of the Mesozoic Betic Basin, SE Spain), constraining the origin and evolution of ore-forming fluids. In Riópar both sulfide and non-sulfide Zn–(FePb) (“calamine”) ores are hosted in hydrothermally dolomitized Lower Cretaceous limestones. The hypogene sulfides comprise sphalerite, marcasite and minor galena. Calamine ores consist of Zn-carbonates (smithsonite and scarce hydrozincite), associated with abundant Fe-(hydr)oxides (goethite and hematite) and minor Pb-carbonates (cerussite). Three smithsonite types have been recognized: i) Sm-I consists of brown anhedral microcrystalline aggregates as encrustations replacing sphalerite; ii) Sm-II refers to brownish subhedral aggregates of rugged appearance related with Fe oxi-hydroxides in the surface crystals, which replace extensively sphalerite; and iii) Sm-III smithsonite appears as coarse grayish botryoidal aggregates in microkarstic cavities and porosity. Hydrozincite is scarce and appears as milky white botryoidal encrustations in cavities replacing smithsonite. Also, two types of cerussite have been identified: i) Cer-I cerussite consists of fine crystals replacing galena along cleavage planes and crystal surfaces; and ii) Cer-II conforms fine botryoidal crystals found infill porosity. Calcite and thin gypsum encrustations were also recognized. The field and petrographic observations of the Riópar non-sulfide Zn–(FePb) revealed two successive stages of supergene ore formation under meteoric fluid processes: i) “gossan” and “red calamine” formation in the uppermost parts of the ore with deposition of Fe-(hydr)oxides and Zn- and Pb-carbonates (Sm-I, Sm-II and Cer-I), occurring as direct replacements of ZnPb sulfides; and ii) “gray calamine” ore formation with deposition of Sm-III, Cer-II and hydrozincite infilling microkarst cavities and porosity. The stable isotope variation of Riópar smithsonite is very similar to those obtained in other calamine-ore deposits around the world. Their CO isotope data (δ¹⁸O: + 27.8 to + 29.6‰ V-SMOW; δ¹³C: − 6.3 to + 0.4‰ V-PDB), puts constrains on: i) the oxidizing fluid type, which was of meteoric origin with temperatures of 12 to 19 °C, suggesting a supergene weathering process for the calamine-ore formation under a temperate climate; and ii) the carbon source, that resulted from mixing between two CO₂ components derived from: the dissolution of host-dolomite (¹³C-enriched source) and vegetation decomposition (¹³C-depleted component).     

Distribution of heavy metals in urban soils – a case study of Danang-Hoian Area (Vietnam)

 This work is part of a research study which is intended to study the degree of anthropogenic influences of the trace metal distribution of soils from Danang-Hoian area (Vietnam). Cu, Ni, Zn and Zr show significant effects in most of the cultivated soil categories, especially in the industrial soils. Extremely high levels of Pb (up to 742 μg/g) are observed in the industrial soil category, which shows an enrichment factor 114 as compared to rural soils. Cd shows only a relative local enrichment with the maximum level of 4.6 μg/g in urban soils. Sequential extraction was performed in selected samples to evaluate the geochemical trace metals. The result indicates that Zn and Cr are mainly found in the crystal and amorphous Fe oxide bounded forms. The contents of Cr in these fractions comprise more than 94% of total extractable Cr. In the case of Zn, 85% of total extractable Zn is in fractions F_V and F_VI. Cu is mainly found in the organic fraction at an average of 39.3% of total extractable content. On the other hand, heavy metal contents show an increasing tendency in the fine fraction (silt and clay). Received: 4 February 1998 · Accepted: 26 November 1998     

Hydrogeological characterization of carbonated Jurassic aquifers in the Gijón-Villaviciosa basin (Asturias,N Spain) by means of geochemical and isotopic techniques

Chemical and isotopic analyses of groundwater from the carbonated Jurassic aquifers in the Gijón-Villaviciosa basin (Asturias, northern Spain) were carried out. Nine springs were sampled to determine major cations and anions, as well as the stable isotopes of the water molecule (δ²H and δ¹⁸O) and sulphate (δ³⁴S) values. Also, δ³⁴S values from gypsum coming both from Triassic rocks and bottom of Jurassic sequence were also determined. The results obtained were used to classify the waters with a genetic criteria in three groups: (1) waters with a high gypsum influence, with sulphate coming from Jurassic gypsum, (2) waters without gypsum influence, where sulphate source could be atmospheric deposition from industrial processes and marine aerosol, and (3) waters with some gypsum influence, in which sulphate origin could be a combination of different sources. In relation to recharge, δ²H and δ¹⁸O values were close to those of Global Meteoric Water Line and fit a local line that suggests a meteoric origin. The estimated elevations for spring recharge are in agreement with those obtained from hydrogeological maps.     

δ<Superscript>18</Superscript>O shifts of geothermal waters in the central of Weihe Basin,NW China

The thermal-waters resources in Weihe Basin of Shaanxi province, NW China are historically classified as middle- to low- temperature thermal-waters in China. Recent exploitation of the deep thermal reservoir in the centre part of the basin (i.e. Xi’an and Xianyang) had observed plentiful supply of thermal fluid with higher measured maximum temperature (120°C) and higher hydraulic pressure (80.50 MPa) in the deeper (more than 4,000 m deep) sedimentary basin. A recent isotope study shows that deep geothermal waters in the cities of Xi’an and Xianyang are characterized by an observable horizontal oxygen-18 (δ¹⁸O) shift and minor deuterium (²H) enrichment. The considerable oxygen shift is possibly due to the following four reasons: water–rock interaction at high temperature, slow circulation rate of water, low water-to-rock ratio, and old age. On the end number of the δ¹⁸O shift, minor δ²H enrichment occur when there is higher concentrations of H₂S, CH₄, I and Br with lower rate of rSO₄ ²⁻/rCl⁻ and r _Na⁺/r _Cl⁻ suggesting relatively isolated geological environment. In a few thermal waters points, r\textNa^\text+ \text/r\textCl^-r{\text{Na}}^{{\text{+}}} {\text{/}}r{\text{Cl}}^{-} < 0.85. This shows possible presence of formation waters. Combining the results from isotopic study and chemical analysis, we can classify the types of geothermal waters into three groups, the shallow and fast circulating system, the semi-circulating system and the deep and slow circulating system.     

Isotopic (Sm–Nd,Pb–Pb,and δ<Superscript>34</Superscript>S) and Geochemical Characteristics of the Metasedimentary Rocks of the Baikal–Patom Belt (Northern Transbaikalia) and Evolution of the Sedimentary Basin in the Neoproterozoic

This paper reports the results of a detailed isotopic (Sm–Nd, Pb–Pb, and δ³⁴S) and geochemical studies of Neoproterozoic metasedimentary rocks from the Patom and Bodaibo domains of the Baikal–Patom belt (northern Transbaikalia). It was shown that the metasedimentary rocks of these domains are strongly variable in their geochemical and isotope geochemical characteristics. Regular variations in these characteristics were observed, and their correlation with the main stages of the evolution of the sedimentary paleobasin in the Neoproterozoic was established.     

Erosion rates evaluated by the <Superscript>137</Superscript>Cs technique in the high altitude area of the Qinghai–Tibet plateau of China

Studying spatial and temporal variation of soil loss is of great importance because of global environmental concerns. Understanding the spatial distribution of soil erosion and deposition in the high-cold steppe is important for designing soil and water conservation measures. Measured ¹³⁷Cs losses (Bq m⁻²) from long-term high altitude (4,000 m above sea level) watershed plots on the Qinghai–Tibet plateau and derived soil erosion estimates (Mg ha⁻¹ year⁻¹) were significantly correlated to directly measured soil losses from the same plots, over the same period (1963–2005). The local reference inventory was estimated to be 2,468 Bq m⁻². The result of analyzing ¹³⁷Cs distribution and its intensity in the soil profiles in this area shows similarities to ¹³⁷Cs distribution in other areas. ¹³⁷Cs is basically distributed in the topsoil layer of 0–0.3 m. Soil erosions vary greatly in the entire sampled area, ranging from 5.5 to 23 Mg ha⁻¹ year⁻¹, with an average of 16.5 Mg ha⁻¹ year⁻¹ which is a moderate rate of erosion.     

Spatial distribution, source identification and affecting factors of heavy metals contamination in urban–suburban soils of Lishui city, China

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.     

Isotopic composition (δ<Superscript>13</Superscript>C and δ<Superscript>18</Superscript>O) and genesis of carbonates from the famennian manganiferous formation of Pai-Khoi

The results of isotope-geochemical studies of carbonates of different mineral types from manganese and host rocks of the Famennian manganiferous formation of Pai-Khoi are reported. Kutnahorite ores are characterized by δ¹³C values from–6.6 to 1.3‰ and δ¹⁸O from 20.0 to 27.4‰. Rhodonite–rhodochrosite rocks of the Silovayakha ore occurrence have δ¹³C from–5.2 to–2.9 and δ¹⁸O from 25.4 to 24.3‰. Mineralogically similar rocks of the Nadeiyakha ore occurrence show the lighter carbon and oxygen isotopic compositions: δ¹³C from–16.4 to–13.1 and δ¹⁸O from 24.8 to 22.5‰. Similar isotopic compositions were also obtained for rhodochrosite–kutnahorite rocks of this ore occurrence: δ¹³C from–13.0 to–10.4‰ and δ¹⁸O from 24.6 to 21.7‰. Siderorodochrosite ores differ in the lighter oxygen and carbon isotopic compositions: δ¹⁸O from 18.7 to 17.6‰ and δ¹³C from–10.2 to–9.3‰, respectively. In terms of the carbon and oxygen isotopic compositions, host rocks in general correspond to marine sedimentary carbonates. Geological-mineralogical and isotope data indicate that the formation of the manganese carbonates was related to the hydrothermal ore-bearing fluids with the light isotopic composition of oxygen and carbon dissolved in CO₂. The isotopic features indicate an authigenic formation of manganese carbonates under different isotopegeochemical conditions.     

The mineral–geochemical evidence of contact transformation of ores of the Dzhusinskoe pyrite–polymetallic deposit (Southern Urals)

The Dzhusinskoe pyrite–polymetallic deposit is characterized by an abundant concentration of dykes of basic and intermediate rocks. Thermal metamorphism of ore-host rocks and the recrystallization of ore minerals are associated with the intrusion of post-ore dykes. A regular increase in the homogenization temperature from 156° at a distance from a dyke to 287–305°C in the contact zone was established. Highly saline (6.4–15.7 wt % NaCl eq.) CO₂–H₂O–NaCl fluids under high pressure (up to 1500 bar) can be associated with the processes of contact and regional metamorphism.     

Geological and geochemical characteristics of the Baimazhai Ni-Cu-（PGE） sulphide deposit in Yunnan, China

The sulphide ores of the Baimazhai deposit, although typically orthomagmatic, locally exhibit peculiar textural features and are intimately associated with hydrothermal minerals, such as biotite, amphibole and chlorite. This association suggests that the magmatic sulphide ores were subjected to hydrothermal alteration and subsequent redistribution, resulting in the observed textural features. Geochemically, the Baimazhai sulphide ores are enriched in Cu, Pd and Au, which,according to previous studies, reflects the action of hydrothermal fluids. Interestingly, Ar-Ar dating yielded the plateau ages of about 160–170 Ma, which are at odds with the established Permian age of the Emeishan large igneous province. We interpreted these younger ages as due to thermal resetting during post-Permian tectonothermal events. We have proposed a model in which tectonic movements and hydrothermal fluids related to these events modified the pre-existing magmatic sulphides. Given the degree of overprint, we suggested two possible scenarios: 1) the sulphide disseminations that surround the massive magmatic ores are the result of deformation and hydrothermal alteration; and 2) there were both magmatic massive and disseminated sulphides, in which case the scale and relocation of remobilization would have been smaller, but still detectable.