An organic geochemical investigation on organic rich sediments from two Neogene formations in the Klias Peninsula area,West Sabah,Malaysia

Twenty organic rich outcrop samples from the Belait and Setap Shale formations in the Klias Peninsula area, West Sabah, were analysed by means of organic petrology and geochemical techniques. The aims of this study are to assess the type of organic matter, thermal maturity and established source rock characterization based primarily on Rock-Eval pyrolysis data. The shales of the Setap Shale Formation have TOC values varying from 0.6 wt%–1.54 wt% with a mean hydrogen index (HI) of 60.1 mg/g, whereas the shal...     

Geochemical characteristics of the Xuanwei Formation in West Guizhou: Significance of sedimentary environment and mineralization

The Upper Permian Xuanwei Formation widely occurs in western Guizhou, unconformably overlying the Emeishan basalts, and mainly consists of black shales. It is ∼170 m thick at Cuyudong Village, Weining County, West Guizhou, China, where the samples of black shale and sandy shale were collected and analyzed. The shales mainly contain SiO₂, 18.9%–44.1%, Al₂O₃, 14.8%–52.8%, Fe₂O₃, 1.0%–41.2%, LOI, 3.2%–21.1%, TiO₂, 1.0%–6.7%, and MgO, 0.2%–2.5%. The contents of all other major elements are lower than 1.0%. It is shown that the black shales have higher contents of Fe₂O₃ and LOI than normal shales. The siderites occurred in the black shales with higher contents of Fe₂O₃, which may be attributed to hydrothermal activities on seafloor. All analyzed shale samples have extremely high Ga, 47.8×10⁻⁶–109.9×10⁻⁶ (70.5×10⁻⁶ on average), higher than the industrial mining standard of Ga Resource Industry Standard. The total contents of rare-earth elements (REE) of 9 black shale samples vary from 213×10⁻⁶ to 1460×10⁻⁶, suggesting that these black shales are enriched in REE. The shale-normalized REE patterns display both positive and negative Ce anomalies (Ce/Ce* from 0.5 to 1.7), revealing that the Xuanwei shales were precipitated under oxic and anoxic conditions. The Rb-Sr chronological diagram of 6 shale samples in the Xuanwei Formation shows an age of 255±12 Ma. Strontium isotopic ratios (⁸⁷Sr/⁸⁶Sr)_t0 range from 0.70635 to 0.70711, suggesting that these Xuanwei black shales might be derived from chemical weathering of the Emeishan basalts.     

Rare-earth and trace element imprints on the origin and tectonic setting of gabbro-diorite complex in the Pan-African belt of Southeast Obudu Plateau,Nigeria

A gabbro-diorite plutonic complex from the Southeast Obudu Plateau, representing limited volumes of magma, was studied for its trace and rare-earth element characteristics, in an attempt to document its genetic and geodynamic history. Geochemical studies indicate that the gabbro samples are characterized by variable concentrations and low averages of such index elements as Cr (40×10-6–200×10-6; av. 80×10-6), Ni (40×10-6–170×10-6; 53.33×10-6) and Zr (110×10-6–240×10-6; 116.67×10-6); variable and high average...     

Carbonization and geochemical characteristics of graphite-bearing rocks in the northern Khanka terrane,primorie, Russian Far East

Regional carbonization was examined in Riphean metamorphic complexes in the northern part of the Khanka terrane. The results obtained by various techniques of physicochemical analysis indicate that all petrographic rock varieties of this complex bear elevated concentrations (from 10⁻⁴ to 10⁻⁶ wt %) of Au and PGE. XRF data were used to describe a wide spectrum of trace elements: Ti, V, Ni, Cr, Pt, Pd, Re, Rh, Os, Ir, Cu, Hg, Au, Ag, Ta, Nb, Sr, Rb, Zr, La, W, Sn, Pb, and Zn. The Rb/Sr-Ba diagram shows the fields of anatectic granite-gneisses, biotite granites, lamprophyres, graphitized crystalline schists, black shales, skarns, and quartz-graphite metasomatic rocks. The C isotopic composition in graphite from the metaigneous rocks (lamprophyres and crystalline schists of the amphibolite facies) corresponds to δ¹³C from −8.5 to −8.7‰, which suggests that the carbon could be of endogenic provenance. The carbon isotopic composition of the greenschist-facies black shales corresponds to δ¹³C from −19.9 to −26.6‰, as is typical of organogenic carbon. The concentrations of precious metals in the rocks are, on average, one order of magnitude lower than in the graphitized crystalline schists. The origin of the precious-metal ore mineralization was likely genetically related to the regional carbonization process.     

Contents of Fixed-Ammonium （ NH4^＋ ） in Lamprophyres in the Zhenyuan Gold Orefield, Yunnan Province, China： Implications for Its Characteristics of the Source Region

This paper determined the fixed-ammonium (NH₄ ⁺) contents of lamprophyres in the Zhenyuan gold orefield, Yunnan Province, China. The results show that the NH₄ ⁺ contents of minettes in the orefield range from 120 × 10⁻⁶ to 469 × 10⁻⁶ and those of kersantites from 74.3 × 10⁻⁶ to 136 × 10⁻⁶. These values are higher than those of other mantle-derived rocks (less than 50 × 10⁻⁶), but lower than those of carbonaceous wall rocks in the orefield (from 1200 × 10⁻⁶ to 1343 × 10⁻⁶). Combining with the Sr isotopic composition, this paper suggested that lamprophyres in the orefield with high NH₄ ⁺ contents relative to other mantle-derived rocks would not have resulted from the primary magma contaminated by crustal materials in the process of rising or in the magma chamber, but from mantel metasomatism. This research project was financially supported jointly by the State Key Basic Research Program of the People’s Republic of China (No. G1999043203) and the Chinese Academy of Sciences Knowledge-Innovation Program (No. KZCX3-SW-125).     

大兴安岭北部甲乌拉铅锌银矿床Rb-Sr同位素测年及其地质意义

甲乌拉铅锌银矿床位于内蒙古自治区满洲里市南西150km。矿床产于中蒙古-额尔古纳兴凯造山带南东缘之得尔布干断裂北西侧。本文在甲乌拉矿床选取7件闪锌矿和6件黄铁矿样品开展了Rb-Sr定年。获得闪锌矿的Rb-Sr等时线年龄为143.0±2.0Ma(MSWD=3.2),锶同位素初始值I Sr=0.71265;黄铁矿的Rb-Sr等时线年龄为142.0±3.0Ma(MSWD=5.7),锶同位素初始值ISr=0.71267;闪锌矿与黄铁矿的Rb-Sr等时线年龄为142.7±1.3Ma(MSWD=3.8),锶同位素初始值ISr=0.71266。上述定年结果表明,甲乌拉矿床形成于早白垩世初期。甲乌拉矿床硫化物的Rb和Sr含量分别介于0.1034×10-6～7.367×10-6和1.301×10-6～7.148×10-6之间,Sr同位素初始比值(87Sr/86Sr)i介于0.71238～0.71277之间,平均值为0.71264,暗示甲乌拉矿床的成矿物质主要来源于地壳。甲乌拉矿床形成于蒙古-鄂霍茨克造山过程的后碰撞阶段。     

Estimation of methane emission from whole waste landfill site using correlation between flux and ground temperature

A methodology to estimate a methane emission in a waste landfill site was developed. The methane flux at a waste landfill site in summer, autumn, and winter was within the following ranges: from −1.3×10⁻² to 16, from −6.4×10⁻² to 7.5, and from −1.6×10⁻³ to 1.5×10⁻² g-CH₄ m⁻² h⁻¹, respectively. In those seasons, the mean methane emission rate and coefficient of variation were 1.1 g-CH₄ m⁻² h⁻¹ ±290%, 0.57 g-CH₄ m⁻² h⁻¹ ±347%, and 5.4×10⁻² g-CH₄ m⁻² h⁻¹ ±370%, respectively. These results simultaneously showed that fluctuations of methane emission from the landfill surface were both of spatial and temporal variability. In each season, an exponential relationship was observed between the methane flux density and the ground temperature. Total methane emissions were estimated to be 5.7×10⁻², 7.1×10⁻³, and 1.7×10⁻³ g-CH₄ m⁻² h⁻¹ in the summer, autumn, and winter surveys, respectively, using a temperature surrogated-kriging method. The results of this study would improve upon the labor-intensive closed-chamber method, and could be a more practical way to estimate methane emissions from waste landfills.     

Trace element geochemistry and tectonic characterization of the granulite facies rocks from Southwest Obudu Plateau,southeastern Nigeria

The trace elements characteristics of the migmatitic gneisses (biotite-garnetand hornblende-biotite), granulite facies rocks (charnockitic gneisses) and meta-peridotite in the area of Southwest Obudu Plateau indicate that the area exhibits a high degree of geochemical variability. Compatible trace elements (Ni and Cr) are comparatively high in the granulite facies rocks and meta-peridotite. Ni ranges from 28×10-6 to 266×10-6 whilst Cr ranges from 62×10-6 to 481×10-6 for the granulite facies rocks (charnocki...     

Rare-earth elements as source indicators of Pan-African granites from Obudu Plateau,Southeastern Nigeria

The rare-earth element （REE） concentrations of representative granite samples from the southeast of the Obudu Plateau, Nigeria, were analyzed with an attempt to determine the signatures of their source, evolutionary history and tectonic setting. Results indicated that the granites have high absolute REE concentrations （190×10^-6-1191×10^-6; av.=549×10^-6） with the chondrite-normalized REE patterns characterized by steep negative slopes and prominent to slight or no negative Eu anomalies. All the samples are also characterized by high and variable concentrations of the LREE （151×10^-6-1169×10^-6; av.= 466×10^-6）, while the HREE show low abundance （4×10^-6-107×10^-6; av.=28×10^-6）. These are consistent with the variable levels of REE fractionation, and differentiation of the granites. This is further supported by the range of REE contents, the chondrite-normalized patterns and the ratios of LaN/YbN （2.30-343.37）, CeN/YbN （5.94-716.87）, LaN/SmN （3.14-11.68） and TbN/YbN （0.58-1.65）. The general parallelism of the REE patterns, suggest that all the granites were comagmatic in origin, while the high Eu/Eu＊ ratios （0.085-2.807; av.=0.9398） indicate high fo2 at the source. Similarly, irregular variations in LaN/YbN, CeN/YbN and Eu/Eu＊ ratios and REE abundances among the samples suggest behaviors that are related to mantle and crustal sources.     

Early Paleozoic adakite in the Liuyuan area from the Beishan orogenic belt,NW Gansu Province: Petrogenesis and implication for tectonic setting

The Liuyuan area,which is located on the southern margin of the Beishan orogenic belt,develops abundant Early Paleozic granitoids.SHRIMP zircon U-Pb dating yielded a weighted mean 206Pb/238U age of 421±8 Ma for the Liuyuan granodiorite(Zhao Zehui et al.,2007),implying its Late Silurian intrusion.Geochemical compositions showed that the Liuyuan granodiorite is characterized by high SiO2(65.01%-67.31%),A12O3(17.17%-18.05%) and Na2O(Na2O/K2O=1.67-1.87) but low Mg# contents calculated as 100×Mg2+/(Mg2++∑Fe2+) from 28.77 to 31.15,as well as being enriched in Sr(472×10-6-517×10-6) but depleted in Yb(1.2×10-6-1.42×10-6) and Y(12.8×10-6-14×10-6).The REEs are characterized by right-inclined patterns with LREE enrichment,HREE depletion and slightly negative Eu anomalies(Eu/Eu*=0.91-0.97).Major and trace elements indicate that the granodiorite is an adakite.The Nb/Ta values of the granodiorite vary from 10.80 to 18.01 and Nb/U from 6.32 to 10.09,both lying between the values of the crust and the mantle.The rock has low εNd(t) values(-2.5--0.8) and high ISr(0.706321-0.706495).Geochemical and Sr-Nd isotopic compositions indicate that the Liuyuan granodiorite is possibly derived from partial melting of thickening lower crust,related to mantle underplating.The Yb-Ta and Y+Nb-Rb discriminant diagrams imply the Liuyuan granodiorite intruded in a local extensional tectonic setting during late collision.Combined with previous studies on geochronology,geochemistry and tectonic setting of granitoids,we interprete that the constraint of this adakite in the Liuyuan area indicates that the tectonic setting may have transformed from collision to extension during the Early Devonian.     

High pressure study of ScAlO3 perovskite

The crystal structure of orthorhombic (Pbnm) ScAlO₃ perovskite has been refined to 5 GPa using single-crystal X-ray diffraction. The compression of the structure if anisotropic with β _a =1.39(3)×10⁻³ GPa⁻¹, β _b =1.14(3)×10⁻³ GPa⁻¹ and β _c =1.84(3)×10⁻³ GPa⁻¹. The isothermal bulk modulus of ScAlO₃, K _T , determined from fitting a Birch-Murnaghan equation of state (K ^′ _T =4) to the volume compression data is 218(1) GPa. The interoctahedral angles to not vary significantly with pressure, and the compression of the structure is entirely attributable to compression of the AlO₆ octahedra. The compressibilities of the constituent AlO₆ and ScO₁₂ are well matched: β_Al−O=1.6×10⁻³ GPa⁻¹ and β_Sc−O=1.5×10⁻³ GPa⁻¹. Therefore the distortion of the structure shows no significant change with increasing pressure. Received: 18 August 1997 / Revised, accepted: 11 November 1997     

Thermal expansion of gehlenite, Ca2Al[AlSiO7], and the related aluminates LnCaAl[Al2O7] with Ln=Tb, Sm

The thermal expansion of gehlenite, Ca₂Al[AlSiO₇], (up to T=830 K), TbCaAl[Al₂O₇] (up to T=1,100 K) and SmCaAl[Al₂O₇] (up to T=1,024 K) has been determined. All compounds are of the melilite structure type with space group Thermal expansion data was obtained from in situ X-ray powder diffraction experiments in-house and at HASYLAB at the Deutsches Elektronen Synchrotron (DESY) in Hamburg (Germany). The thermal expansion coefficients for gehlenite were found to be: α₁=7.2(4)×10⁻⁶ K⁻¹+3.6(7)×10⁻⁹ΔT K⁻² and α₃=15.0(1)×10⁻⁶ K⁻¹. For TbCaAl[Al₂O₇] the respective values are: α₁=7.0(2)×10⁻⁶ K⁻¹+2.0(2)×10⁻⁹ΔT K⁻² and α₃=8.5(2)×10⁻⁶ K⁻¹+2.0(3)×10⁻⁹ΔT K⁻², and the thermal expansion coefficients for SmCaAl[Al₂O₇] are: α₁=6.9(2)× 10⁻⁶ K⁻¹+1.7(2)×10⁻⁹ΔT K⁻² and α₃=9.344(5)×10⁻⁶ K⁻¹. The expansion-mechanisms of the three compounds are explained in terms of structural trends obtained from Rietveld refinements of the crystal structures of the compounds against the powder diffraction patterns. No structural phase transitions have been observed. While gehlenite behaves like a ’proper’ layer structure, the aluminates show increased framework structure behaviour. This is most probably explained by stronger coulombic interactions between the tetrahedral conformation and the layer-bridging cations due to the coupled substitution (Ca²⁺+Si⁴⁺)-(Ln ³⁺+Al³⁺) in the melilite-type structure. Electronic Supplementary Material Supplementary material is available for this article at     

Thermal expansion of gehlenite, Ca2Al[AlSiO7], and the related aluminates LnCaAl[Al2O7] with Ln = Tb, Sm

The thermal expansion of gehlenite, Ca₂Al[AlSiO₇], (up to T=830 K), TbCaAl[Al₂O₇] (up to T=1100 K) and SmCaAl[Al₂O₇] (up to T=1024 K) has been determined. All compounds are of the melilite structure type with space group Thermal expansion data were obtained from in situ X-ray powder diffraction experiments in-house and at HASYLAB at the Deutsches Elektronen Synchrotron (DESY) in Hamburg (Germany). The thermal expansion coefficients for gehlenite were found to be: α₁=7.2(4)×10⁻⁶×K⁻¹+3.6(7)×10⁻⁹ΔT×K⁻² and α₃=15.0(1)×10⁻⁶×K⁻¹. For TbCaAl[Al₂O₇] the respective values are: α₁=7.0(2)×10⁻⁶×K⁻¹+2.0(2)×10⁻⁹ΔT×K⁻² and α₃=8.5(2)×10⁻⁶×K⁻¹+2.0(3)×10⁻⁹ΔT×K⁻², and the thermal expansion coefficients for SmCaAl[Al₂O₇] are: α₁=6.9(2)×10⁻⁶×K⁻¹+1.7(2)×10⁻⁹ΔT×K⁻² and α₃=9.344(5)×10⁻⁶×K⁻¹. The expansion mechanisms of the three compounds are explained in terms of structural trends obtained from Rietveld refinements of the crystal structures of the compounds against the powder diffraction patterns. No structural phase transitions have been observed. While gehlenite behaves like a ‘proper’ layer structure, the aluminates show increased framework structure behavior. This is most probably explained by stronger coulombic interactions between the tetrahedral conformation and the layer-bridging cations due to the coupled substitution (Ca²⁺+Si⁴⁺)–(Ln ³⁺+Al³⁺) in the melilite-type structure. This article has been mistakenly published twice. The first and original version of it is available at .     

Chemical and Strontium Isotopic Compositions of the Hanjiang Basin Rivers in China: Anthropogenic Impacts and Chemical Weathering

The Hanjiang River, the largest tributaries of the Changjiang (Yangtze) River, is the water source area of the Middle Route of China’s South-to-North Water Transfer Project. The chemical and strontium isotopic compositions of the river waters are determined with the main purpose of understanding the contribution of chemical weathering processes and anthropogenic inputs on river solutes, as well as the associated CO₂ consumption in the carbonate-dominated basin. The major ion compositions of the Hanjiang River waters are characterized by the dominance of Ca²⁺ and HCO₃ ⁻, followed by Mg²⁺ and SO₄ ²⁻. The increase in TDS and major anions (Cl⁻, NO₃ ⁻, and SO₄ ²⁻) concentrations from upstream to downstream is ascribed to both extensive influences from agriculture and domestic activities over the Hanjiang basin. The chemical and Sr isotopic analyses indicate that three major weathering sources (dolomite, limestone, and silicates) contribute to the total dissolved loads. The contributions of the different end-members to the dissolved load are calculated with the mass balance approach. The calculated results show that the dissolved load is dominated by carbonates weathering, the contribution of which accounts for about 79.4% for the Hanjiang River. The silicate weathering and anthropogenic contributions are approximately 12.3 and 6.87%, respectively. The total TDS fluxes from chemical weathering calculated for the water source area (the upper Hanjiang basin) and the whole Hanjiang basin are approximately 3.8 × 10⁶ and 6.1 × 10⁶ ton/year, respectively. The total chemical weathering (carbonate and silicate) rate for the Hanjiang basin is approximately 38.5 ton/km²/year or 18.6 mm/k year, which is higher than global mean values. The fluxes of CO₂ consumption by carbonate and silicate weathering are estimated to be 56.4 × 10⁹ and 12.9 × 10⁹ mol/year, respectively.     

Geochemical and Sr-Nd isotopic study of alkaline syenites in Liangtun-Kuangdonggou, Liaoning Province, China： Evidence for enriched mantle before 1.86 Ga and implications

The 1.86 Ga Liangtun-Kuangdonggou complex (LKC) is one of the oldest alkaline syenite bodies so far discovered in China. This syenite suite has elevated contents of total alkali (K2O Na2O), with an average of 10.50%, and a mean Rittmann Index (σ) of 6.48. The intrusions have slightly higher concentrations of K2O than those of Na2O on a weight percent basis, indicating the rocks belong to potassium-rich alkaline syenite series. Total rare-earth element concentrations (∑REE ) of the rocks are relatively high, ranging from 324×10 -6 to 1314×10 -6, with a mean value of 666×10 -6. The REE patterns are subparallel and rightward steep with (La/Yb)N >33, showing mild negative to positive Eu anomalies (δEu: 0.63-1.15). All samples exhibit strong LILE and LREE enrichments and TNT (Nb, Ta, Ti) and P depletions in multi-element spidergrams. On the εSr(t)-εNd(t) correlation diagram, most analytical data points plot within the enriched mantle field with low ( 87Sr/86Sr)i ratios (0.7045-0.7051) and negative εNd(t) values (-3.72--3.97), falling among those kimberlites from Fuxian County, Liaoning Provinve, from Mengyin County, Shandong Province and the Ⅱ-type kimberlites from South Africa. These characteristics imply that the LKC-rocks may have the same source as the above-mentioned kimberlites, i.e., they have close connections to the materials derived from enriched mantle reservoirs, further revealing that the upper mantle beneath the northeastern part of the North China Plate had been highly enriched before 1.86 Ga. Geodynamically, the LKC-rocks were formed in a within-plate environment with close genetic connections to rift-related alkaline magma activities possibly controlled by ancient mantle plumes.     

内蒙古乌兰沟埃达克岩锆石U-Pb年龄及构造环境

内蒙古中部贺根山缝合带的梅劳特乌拉蛇绿岩中,新发现乌兰沟埃达克岩,岩性为花岗闪长岩。LA-ICP-MS锆石UPb测年结果表明,乌兰沟埃达克岩的侵位年龄为279.3±1.4Ma,其形成时代为早二叠世。乌兰沟埃达克岩SiO_2含量为65.92%~69.65%,MgO为1.34%~2.16%,Al_2O_3为15.30%~17.33%,Na_2O/K_2O值为3.95~14.09,Sr=359.60×10~(-6)~734.00×10~(-6),Yb=0.83×10~(-6)~2.02×10~(-6),Y=6.65×10~(-6)~12.84×10~(-6);富集K、Rb、Sr等大离子亲石元素,亏损Nb、Ta、Ti、P等高场强元素;稀土元素总量为32.18×10~(-6)~65.41×10~(-6),明显较低,轻、重稀土元素分馏明显,(La/Yb)N值为2.84~7.56,无明显Eu异常,显示出高硅埃达克岩(HSA)的地球化学特征。该埃达克岩具有岛弧型岩浆岩特征,形成于俯冲带岛弧环境,可能为洋内俯冲洋壳+俯冲深积物部分熔融并与上覆地幔楔橄榄岩反应成因。根据乌兰沟埃达克岩与梅劳特乌拉蛇绿岩的时空分布与演化特征,贺根山缝合带在早二叠世可能存在洋内俯冲作用。     

埃达克岩的研究现状及其趋势

达克岩(adakite)是一种中酸性富钠火成岩(安山岩、英安岩、钠质流纹岩及相应的侵入岩),其突出的地球化学特征就是SiO2≥56%,Al2O3≥15%,低重稀土元素(HREE)与Y(如Yb≤1.9×10-6,Y≤18×10-6),高Sr(大多数>400×10-6,La/Yb(≥10.0)与Sr/Y(>20.0～40.0),一般具有正铕异常(少数具有极弱负铕异常).埃达克岩存在两种成因类型:一种由俯冲的年轻(≤25～30Ma)大洋板片熔融形成(O型埃达克岩);另一种由增厚地壳环境中的玄武质下地壳熔融形成(C型埃达克岩).文章从埃达克岩的特征、形成机制、成矿作用、构造背景、动力学意义等几个方面论述了埃达克岩的研究现状,并指出了未来埃达克岩研究的趋势.     

The Gumeshevo skarn-porphyry copper deposits in the Central Urals,Russia: Evolution of the ore-magmatic system as deduced from isotope geochemistry (Sr,Nd, C,O, H)

The Early Devonian Gumeshevo deposit is one of the largest ore objects pertaining to the dioritic model of the porphyry copper system paragenetically related to the low-K quartz diorite island-arc complex. The (⁸⁷Sr/⁸⁶Sr)_t and (ɛ_Nd)_t of quartz diorite calculated for t = 390 Ma are 0.7038–0.7045 and 5.0–5.1, respectively, testifying to a large contribution of the mantle component to the composition of this rock. The contents of typomorphic trace elements (ppm) are as follows: 30–48 REE sum, 5–10 Rb, 9–15 Y, and 1–2 Nb. The REE pattern is devoid of Eu anomaly. Endoskarn of low-temperature and highly oxidized amphibole-epidote-garnet facies is surrounded by the outer epidosite zone. Widespread retrograde metasomatism is expressed in replacement of exoskarn and marble with silicate (chlorite, talc, tremolite)-magnetite-quartz-carbonate mineral assemblage. The ⁸⁷Sr/⁸⁶Sr ratios of epidote in endoskarn and carbonate in retrograde metasomatic rocks (0.7054–0.7058 and 0.7053–0.7065, respectively) are intermediate between the Sr isotope ratios of quartz dioritic rocks and marble (⁸⁷Sr/⁸⁶Sr = 0.70784 ± 2). Isotopic parameters of the fluid equilibrated with silicates of skarn and retrograde metasomatic rocks replacing exoskarn at 400°C are δ¹⁸O = +7.4 to +8.5‰ and δD = −49 to −61‰ (relative to SMOW). The δ¹³C and δ¹⁸O of carbonates in retrograde metasomatic rocks after marble are −5.3 to +0.6 (relative to PDB) and +13.0 to +20.2% (relative to SMOW), respectively. Sulfidation completes metasomatism, nonuniformly superimposed on all metasomatic rocks and marbles with formation of orebodies, including massive sulfide ore. The δ³⁴S of sulfides is 0 to 2‰ (relative to CDT);⁸⁷Sr/⁸⁶Sr of calcite from the late calcite-pyrite assemblage replacing marble is 0.704134 ± 6. The δ¹³C and ⁸⁷Sr/⁸⁶Sr of postore veined carbonates correlate positively (r = 0.98; n = 6). The regression line extends to the marble field. Its opposite end corresponds to magmatic (in terms of Bowman, 1998b) calcite with minimal δ¹³C, δ¹⁸O, and ⁸⁷Sr/⁸⁶Sr values (−6.9 ‰, +6.7‰, and 0.70378 ± 4, respectively). The aforementioned isotopic data show that magmatic fluid was supplied during all stages of mineral formation and interacted with marble and other rocks, changing its Sr, C, and O isotopic compositions. This confirms the earlier established redistribution of major elements and REE in the process of metasomatism. A contribution of meteoric and metamorphic water is often established in quartz from postore veins.     

相山铀矿田西部地区深部多金属矿化成矿年代与成矿流体演化:Rb-Sr同位素体系的制约

江西相山铀矿田科学深钻3号孔在深部-700 m发现大量铅锌多金属矿化脉,垂向上呈"上铀下多金属"的分布特征。本文选取深部多金属矿脉主成矿阶段(S3)自形闪锌矿样品6件和不同阶段的毒砂、黄铁矿、方铅矿、方解石等样品12件,以及围岩全岩样品17件,进行了Rb、Sr同位素组成研究。结果表明:(1)由闪锌矿Rb-Sr等时线法确定的相山铀矿田深部多金属矿化形成于121. 0±3. 5Ma,与围岩火山岩存在较大时差,可能与晚于围岩的深部次火山有关。根据穿插关系,多金属矿化略晚于碱性交代铀矿化,但明显早于酸性交代铀矿化;(2)多金属矿化脉体中金属矿物的Rb和Sr含量分别介于0. 041×10~(-6)～1. 38×10-6和2. 35×10-6～23. 11×10-6之间,Sr同位素初始比值(87Sr/86Sr)i变化较大,介于0. 706114～0. 718814之间,平均值为0. 713579,暗示相山铀矿田深部多金属矿化的成矿物质主要来源于地壳。初始流体Sr同位素值(0. 718665)明显高于成矿时赋矿围岩(流纹英安岩为0. 714581,碎斑流纹岩为0. 714417)的Sr同位素组成,表明多金属成矿流体和物质并非来自围岩火山岩;(3)由早到晚阶段的(87Sr/86Sr)i呈明显降低的演化趋势,表明成矿流体演化过程中受到大气降水的不断稀释作用。相山矿田的铀矿和深部多金属矿化同形成于华南中生代板内伸展构造背景。     

Thermodynamics of arsenates,selenites, and sulfates in the oxidation zone of sulfide ores: Part III: Eh-pH diagrams of the Me-As-H<Subscript>2</Subscript>O systems (Me = Co,Ni, Fe,Cu, Zn,Pb) at 25°C

The behavior of arsenic at the Earth’s surface and nearby at low temperatures and pressures depends mainly on the redox potential and the acidity-alkalinity of the crystallization media. These parameters determine the migration of arsenic compounds and their precipitation as various solid phases. Understanding the mechanism of arsenic’s behavior under surface conditions, which is important for solving environmental problems, is an urgent task of contemporary mineralogy and geochemistry. The activities of the components in natural waters beyond the zones of natural (oxidation zones) and man-made contamination with arsenic (a _ΣAs = 3 × 10⁻⁸, a _ΣFe = 10⁻⁵, a _ΣCu = 10⁻⁷, a _ΣZn = 5 × 10⁻⁷, a _ΣCo = 10⁻⁸, a _ΣNi = 6 × 10⁻⁸, a _ΣPb = 10⁻⁸) and in waters formed in the oxidation zone (a _ΣSe = 10⁻³, a _ΣFe = 10⁻², a _ΣCu = 10⁻², a _ΣZn = 5 × 10⁻², a _ΣCo = 10⁻³, a _ΣNi = 10⁻², a _ΣPb = 10⁻⁴) have been estimated. Eh-pH diagrams were calculated and plotted using the Geochemist’s Workbench (GMB 7.0) software package. The database comprises the thermodynamic parameters of 46 elements, 47 main particles, 48 redox pairs, 551 particles in solution, 624 solid phases, and 10 gases. The Eh-pH diagrams of the Me-As-H₂O systems (Me = Co, Ni, Fe, Cu, Zn, Pb) were plotted for the average contents of these elements in the underground water and for their higher contents in the oxidation zones of sulfide deposits. The formation of Co, Ni, Fe, Cu, Zn, and Pb arsenates at the surface is discussed.