The corrosion of basaltic dykes in evaporites: Ar–Sr–Nd isotope and rare earth elements evidence

The corrosion of basaltic dykes from central Germany which intruded during the Tertiary into rock and potash salts of Upper Permian age (Zechstein) has been studied. The corrosion behavior of these glassy basalts can serve as a natural analogue for the long-term corrosion expected for nuclear waste glasses in a salt repository. Our data demonstrate mobility and fractionation of the rare earth elements (REE) during a postintrusive circulation of salt brines. The processes controlling this behavior of the REE were dissolution and reprecipitation of phosphates. The K–Ar data document the synintrusive assimilation of a salt phase followed by a postintrusive fluid circulation in the peripheral parts. This circulation removed the assimilated salt and imported highly radiogenic salt Ar which was integrated into newly formed sheet silicates. The central part of the dyke was not affected by this circulation and could retain a mantle gas phase. The Sr isotope data document a synintrusive assimilation of salt Sr and a strong exchange with salt fluids during the postintrusive corrosion which was strongest in a zone next to the chilled dyke margins. This locally stronger alteration is probably due to different cooling and shrinking rates of the basalt at the margins and in the core of the dyke which led to the formation of a highly permeable fractured zone.     

滇西南那邦变质基性岩地球化学与俯冲板片裂离

中缅边界那邦麻粒岩相变质基性岩地球化学特征表明其原岩是岩浆岩,并具有ＭＯＲＢ的特性,其岩石化学具有以下特征：岩石的ＴＦｅ／ＭｇＯ值低（１．１０～２．１７）,ＡＦＭ图解上显示拉斑玄武岩演化趋势;ＴｉＯ２含量（１．１４％～１．８１％）高稀土亏损、重稀土较有富集的配分形式,稀土元素和总量（∑ＲＥＥ）值十倍于球粒陨石（２４～５０μｇ／ｇ）,（Ｌａ／Ｓｍ）Ｎ＝０．４３～０．７５（Ｌａ／Ｙｂ）Ｎ＝０．４５～０     

Geochemical Characteristics and Genesis of the Luxi-Xianrenzhang Diabase Dikes in Xiazhuang Uranium Orefield, Northern Guangdong Province

The Luxi-Xianrenzhang diabase dikes were emplaced into the eastern part of the Guidong composite granitoids in northern Guangdong Province at the end of the Early Cretaceous. They show tholeiitic features, enrichment in large ion lithophile elements, slight enrichment in light rare earth elements, depletion in Zr and Hf, and basically no depletion in Nb and Ta and no Eu anomaly. They are similar to intraplate basalt in terms of trace element characteristics. They have high εNd（t） values （3.6-4.9）, initial ^87Sr/^86Sr ratios （0.70530-70641） and δ^18O values and Dupal anomaly of Pb isotope compositions. Their Sr-Nd, Pb-Sr, Pb-Nd and Pb-Pb isotopes plot between DMM and EMII, with Pb similar to EMII, Nd relatively close to DMM and Sr in between. This profile suggests that the diabase dikes studied were derived from partial melting of a mantle source that had been subjected to metasomatism by fluids originated from a subduction zone under a tectonic environment of crustal extension and lithosphere thinning in the late Yanshanian.     

Characterization and migration of atmospheric REE in soils and surface waters

Rainwater and snow collected from three different sites in France (Vosges Mountains, French Alps and Strasbourg) show more or less similar shapes of their REE distribution patterns. Rainwater from Strasbourg is the most REE enriched sample, whereas precipitations from the two mountainous, less polluted catchments are less REE enriched and have concentrations close to seawater. They are all strongly LREE depleted.Different water samples from an Alpine watershed comprising snow, interstitial, puddle and streamwater show similar REE distributions with LREE enrichment (rainwater normalized) but MREE and HREE depletion. In this environment, where water transfer from the soil to the river is very quick due to the low thickness of the soils, it appears that REE in streamwater mainly originate from atmospheric inputs. Different is the behaviour of the REE in the spring- and streamwaters from the Vosges Mountains. These waters of long residence time in the deep soil horizons react with soil and bedrock REE carrying minerals and show especially significant negative Eu anomalies compared to atmospheric inputs. Their Sr and Nd isotopic data suggest that most of the Sr and Nd originate from apatite leaching or dissolution. Soil solutions and soil leachates from the upper soil horizons due to alteration processes strongly depleted in REE carrying minerals, have REE distribution patterns close to those of lichens and throughfall. Throughfall is slightly more enriched especially in light REE than filtered rainwater probably due to leaching of atmospheric particles deposited on the foliage and also to leaf excretion.Data suggest that Sr and Nd isotopes of the soil solutions in the upper soil horizons originate from two different sources: 1) An atmospheric source with fertilizer, dust and seawater components and 2) A source mainly determined by mineral dissolution in the soil. These two different sources are also recognizable in the Sr and Nd isotopic composition of the tree’s throughfall solution. The atmospheric contributions of Sr and Nd to throughfall and soil solution are of 20 to 70 and 20%, respectively. In springwater, however, the atmospheric Sr and REE contribution is not detectable.     

Tertiary basalts and peridotite xenoliths from the Hessian Depression (NW Germany), reflecting mantle compositions low in radiogenic Nd and Sr

A total of 17 alkali basalts (alkali olivine basalt, limburgite, olivine nephelinite) and quartz tholeiites, and of 10 peridotite xenoliths (or their clinopyroxenes) were analyzed for Nd and Sr isotopes. ¹⁴³Nd/¹⁴⁴Nd ratios and ⁸⁷Sr/⁸⁶Sr ratios of all basalts and of the majority of ultramafic xenoliths plot below the mantle array with a large variation in Nd isotopes and a smaller variation in Sr isotopes. The tholeiites were less radiogenic in Nd than the alkali basalts. Volcanics from the Eifel and Massif Central regions contain Nd and Sr, which is more radiogenic than that of the basalts from the Hessian Depression. Nd and Sr isotopic compositions of all rocks from the latter area, with the exception of one tholeiite and one peridotite plot in the same field of isotope ratios as the Ronda ultramafic tectonite (SW Spain), which ranges in composition from garnet to plagioclase peridotite. The alkali basaltic rocks are products of smaller degrees of partial melting of depleted peridotite, which has undergone a larger metasomatic alteration compared with the source rock of tholeiitic magmas. For the peridotite xenoliths such metasomatic alteration is indicated by the correlation of their K contents and isotopic compositions. We assume that the upper mantle locally can acquire isotopic signatures low in radiogenic Nd and Sr from the introduction of delaminated crust. Such granulites low in radiogenic Nd and Sr are products of early REE fractionation and granite (Rb) separation.     

湖南锡矿山锑矿矿区煌斑岩的地球化学特征

对湖南锡矿山矿区煌斑岩脉进行了系统的元素和同位素地球化学研究，来探讨煌斑岩的成因。本区煌斑岩形成时代大约为120Ma，早于锑成矿时间，并与锑成矿有密切相关。其微量元素MORB蛛网图，以富集高场强元素，Nb-Ta亏损和Ti不亏损，Th强富集和Ce弱富集为特征，具有岛弧型玄武岩微量元素分配模式，构造环境可能为大陆内部破坏板块边缘。稀土元素具有总量高，无明显的负铕异常，配分模式呈轻稀土富集的右倾型特征。同位素以高^87Sr/^86Sr、低^143Nd/^144Nd为特征。结合元素地球化学、同位素特征和地质发展史分析，煌斑岩可能为富含REE和高场强元素的俯冲带流体交代过的富集地幔部分熔融所产生的岩浆，在上升过程中同化和混合很少量的矿区隐伏花岗岩浆和灰岩的产物。     

Geochemical Constrains on Petrogenesis and Tectonic Setting of Volcanic Rocks from the Baimianxia and Sanwan Formations in the Northern Margin of the Yangtze Plate

On the basis of petrogeochemical data, the volcanic lavas of the Baimianxia Formation can be classified into two units: high TiO2 and low TiO2. The TiO2 concentration of the former is generally higher than 1%, which occurs in the lower part with high-grade metamorphism, but the latter is less than 1% and crops out in the upper part with low-grade metamorphism. The high-TiO2 unit is dominated by tholeiitic lavas showing high rare earth element (REE) contents (ΣREE?=?83.4–180.8?μg/g), high light/heavy REE (LREE/HREE) ratios (LREE/HREE=2.17–5.85) and weak negative Eu anomaly (Eu=0.79–1.01). Its trace element patterns display weak Nb-Ta anomalies with respect to Th, K, La, Ce, showing within-plate basalt affinities. In contrast, the low-TiO2 unit is characterized by low REE contents, low LREE/HREE ratios, and pronounced Nb-Ta anomalies, indicating typical arc or continental arc signature. Chondrite-normalized REE patterns of basalts and andesites from the Sanwan Formation are flat or LREE depletion, which is very similar to normal mid-oceanic basalt. Therefore, we suggest that these lavas should be formed in a back-arc basin setting. Sr-Nd isotopic data of the basalt in the lower part suggest that the rocks would have been formed in ~1144?Ma. Based on the geochemical and isotopic features of the basalts, we suggest that these rocks in the low part of the Baimianxia Formation should originate from an asthenospheric oceanic-island basalt-like mantle source, which may be produced by partial melting of garnet lherzolite, and significantly underwent fractional crystallization and crustal or lithospheric mantle contamination en route to the surface. However, laser ablation inductively coupled plasma mass spectrometry zircon U-Pb dating of the basalt sample from the upper part of the Baimianxia Formation gives a 437 Ma, indicating a Early Paleozoic age. The geochemical analysis in this paper suggests that they may originate from an arc or continental arc in response to aqueous fluids or melt expelled from a subducting slab, and the partial melting occurred in the garnet stability field. The samples of basalts and andesites in the Sanwan Formation show they are derived from depleted mantle source similar to normal mid-oceanic basalt. Finally, we can conclude that the lavas in the lower part of the Baimianxia Formation represent the geological records of rift-related volcanism in the middle Proterozoic, which is commonly considered to be the precursor of continental breakup and followed by oceanic basin forming from Neoproterozoic to early Paleozoic. Whereas, the lavas in upper part of the Baimianxia Formation and Sanwan Formations may have been generated by the oceanic and continental conversion that occurred in the early Paleozoic.     

Trace element and isotope geochemistry of depleted peridotites from an N-MORB type ophiolite (Internal Liguride,N. Italy)

 Mantle peridotites of the Internal Liguride (IL) units (Northern Apennines) constitute a rare example of the depleted lithosphere of the Jurassic Ligurian Tethys. Detailed chemical (ICP-MS and SIMS techniques) and isotopic investigations on very fresh samples have been performed with the major aim to constrain the timing and mechanism of their evolution and to furnish new data for the geodynamic interpretation. The data are also useful to discuss some general geochemical aspects of oceanic-type mantle. The studied samples consist of clinopyroxene-poor spinel lherzolites, showing incipient re-equilibration in the plagioclase-facies stability field. The spinel-facies assemblage records high (asthenospheric) equilibration temperatures (1150–1250° C). Whole rocks, and constituent clinopyroxenes, show a decoupling between severe depletion in highly incompatible elements [light rare earth elements (LREE), Sr, Zr, Na, Ti] and less pronounced depletion in moderate incompatible elements (Ca, Al, Sc, V). Bulk rocks also display a relatively strong M(middle)REE/H(heavy)REE fractionation. These compositional features indicate low-degree (<10%) fractional melting, which presumably started in the garnet stability field, as the most suitable depletion mechanism. In this respect, the IL ultramafics show strong similarity to abyssal peridotites. The Sr and Nd isotopic compositions, determined on carefully handpicked clinopyroxene separates, indicate an extremely depleted signature (⁸⁷Sr/⁸⁶Sr=0.702203–0.702285; ¹⁴³Nd/¹⁴⁴Nd=0.513619–0.513775). The Sm/Nd model ages suggest that the IL peridotites melted most likely during Permian times. They could record, therefore, the early upwelling and melting of mid ocean ridge basalt (MORB) type asthenosphere, in response to the onset of extensional mechanisms which led to the opening of the Western Tethys. They subsequently cooled and experienced a composite subsolidus evolution testified by multiple episodes of gabbroic intrusions and HT-LP retrograde metamorphic re-equilibration, prior to their emplacement on the sea floor. The trace element chemistry of IL peridotites also provides useful information about the composition of oceanic-type mantle. The most important feature concerns the occurrence of Sr and Zr negative anomalies (relative to “adjacent” REE) in both clinopyroxenes and bulk rocks. We suggest that such anomalies reflect changes in the relative magnitude of Sr, Zr and REE partition coefficients, depending on the specific melting conditions. Received: 15 February 1995/Accepted: 4 August 1995     

Rare earth element behavior and Pb,Sr, Nd isotope systematics in a heavy metal contaminated soil

The aim of this study is to characterize the processes and phases which control migration and retention of rare earth elements (REE) in a heavy metal contaminated soil. In addition to concentration data, we used Pb, Sr and Nd isotopic compositions in order to distinguish between natural and anthropogenic trace metals and to characterize the phases leached away during the sequential extraction procedure.The samples were sequentially extracted in 3 steps with 1 N acetic acid (HAc), 1 N HCl and 1 N HNO₃. The Pb isotope data showed that anthropogenic Pb had mainly been retained in the uppermost 10 cm by the organic matter of the topsoil. The⁸⁷Sr/⁸⁶Sr ratios of the HAc extracts are almost constant and indicate that soil carbonate is derived from regionally outcropping carbonate-rich sediments. Most HCl and HNO₃ extracts have more radiogenic Sr isotopic compositions, but it is unclear whether this reflects a growing influence of anthropogenic or silicate-derived Sr.The depth distribution of the REE is mainly controlled by two different parameters: soil pH for the HAc extractable REE and FeMn oxides for the REE in the HCl and HNO₃ extracts. A part of the HNO₃ extractable REE was also bound to the organic matter of the topsoil. The REE concentrations in the HAc extractable phase increase with depth and increasing soil pH, which indicates that they are derived from the surface and hence are of anthropogenic origin. This is confirmed by¹⁴³Nd/¹⁴⁴Nd isotope ratios which show a mixing between a natural end-member at the top and an anthropogenic end-member at the base of the profile. We assume that the anthropogenic REE were transported in dissolved form as carbonate complexes and then precipitated during downward migration as soil pH increased.     

Petrology and geochemistry of komatiites and tholeiites from Gorgona Island,Colombia

Komatiitic rocks from Gorgona Island, Colombia, in contrast to their Archaean counterparts, occur as rather structureless flows. In addition, textural and mineralogical features indicate that the Gorgona komatiites may have crystallized from superheated liquids. Komatiitic rocks have MgO contents which range from 24 to 11 wt.% and plot on well-defined olivine (Fo₉₀) control lines. Calculations show that potential evolved liquids (MgO<11 wt%) will be SiO₂-poor. Komatiites, in this case, cannot be regarded as parental to the associated tholeiitic basalt sequence.On the basis of REE concentrations and Sr, Nd isotopic compositions, the associated basalts are found to be of two types. One type (K-tholeiite) is characterized by noticeably fractionated REE patterns and relatively primitive isotopic compositions similar to those of the komatiites. K-tholeiites, together with komatiites, are regarded as comprising a distinctive komatiitic suite. REE patterns within this suite show progressive depletion in the LREE from K-tholeiites to komatiites, and represent increasingly higher degrees of melting of the same mantle source region. The other type (T-tholeiite), representative of the bulk of the exposed basalt sequence, has flat REE patterns and relatively evolved isotopic compositions. This tholeiitic suite is clearly genetically unrelated to the komatiitic suite.     

Coupled Ce-Nd isotope systematics and rare earth elements differentiation of the moon

¹³⁸Ce/¹⁴²Ce and ¹⁴³Nd/¹⁴⁴Nd isotope ratios of lunar samples are determined to constrain the petrogenetic differentiation and evolution of the moon. High-precision Ce-Nd isotope data, well-defined Rb-Sr isochrons, and rare earth elements (REE) abundances of lunar samples show that unexpectedly low La/Ce ratios of evolved lunar highland samples are preserved from at least 3.9 Ga. Precise analysis of REE abundances indicates that the low La/Ce ratio results from a depletion of La relative to other REE. This depletion can be seen in pristine KREEP basalts and Mg-suite rocks from 3.85 to 4.46 Ga. As REE abundances of all these samples are controlled by the presence of a KREEP component, the depletion was probably inherited from a late crystallization sequence of the lunar magma ocean related to the production of the original KREEP component.     

Rare earth elements, yttrium and H, O, C, Sr, Nd and Pb isotope studies in mineral waters and corresponding rocks from NW-Bohemia, Czech Republic

The sparkling waters from the area of Kyselka near Karlovy Vary at the western slope of the Doupovske hory, Bohemia (Czech Republic), and CO₂-poor waters from two underground boreholes at Jachymov, Krusne hory, Bohemia, have been studied with the aim of characterizing the distribution of rare earth elements, yttrium, and H, O, C, Sr, Nd, Pb isotopes during the low-temperature alteration processes of the host rocks. Additionally, leaching experiments were performed at pH 3 on the granitic and basaltic host rocks from Kyselka and the granite of Jachymov. All REE patterns of the granite- and the basalt-derived waters from the Kyselka area are different from those of their source rocks and the leachates of the latter. This elucidates the inhomogeneous distribution of REE and Y among the solid phases in the altered magmatic rocks. The Eu and Ce anomalies in granite-derived waters are inherited, the Y anomaly is achieved by fluid migration. Yttrium is always preferentially leached by mineral waters, whereas Y/Ho ratios of rocks and their leachates are very similar. The REE abundances in waters from the wells in Jachymov are derived from rocks intensely leached and depleted in easily soluble REE-bearing minerals, whereas the granites and basalts from Kyselka still contain soluble, REE-bearing minerals. A comparison of REE/Ca patterns of the experimental leachates with those of the mineral waters elucidate the high retention of REE in rocks during water–rock interaction. In strongly altered rocks Sr isotope ratios of mineral waters and rocks differ widely, whereas the corresponding Nd isotope ratios are very similar. ²⁰⁷Pb/²⁰⁸Pb, ²⁰⁶Pb/²⁰⁸Pb and ²⁰⁶Pb/²⁰⁷Pb ratios in mineral waters are independent from U/Th ratios in the rocks. ²⁰⁶Pb/²⁰⁸Pb and ²⁰⁶Pb/²⁰⁷Pb are lower in mineral waters than in their source rocks and their leachates, which indicates that Pb is primarily derived from solid phases that do not contain significant contents of leachable U and Th. Thus, mineral waters, although CO₂ rich, only interact with surface films on minerals and not with the bulk of the minerals as in the leaching experiments.Calculation of mixing ratios of waters from the granitic and basaltic sources of the waters from the Kyselka area yield about 40% of water from the underlying granite in water recovered from the basalt, whereas the granite-derived water is mixed with only about 5% of the water from the basalt.     

Major and trace element, and Sr-Nd isotope constraints on the origin of Paleogene volcanism in South China prior to the South China Sea opening

Paleogene volcanic rocks crop out in three sedimentary basins, namely, Sanshui, Heyuan and Lienping, in the attenuated continental margin of south China. Lavas from the Sanshui basin which erupted during 64-43 Ma are bimodal, consisting of intraplate tholeiitic basalt and trachyte/rhyolite associations. Similar to Cretaceous A-type granites from the nearby region, the felsic member shows peralkaline nature [Na₂O + K₂O ≈ 10–12%; (Na + K)/Al≈ 0.98−1.08], general enrichment in the incompatible trace elements and significant depletion in Ba, Sr, Eu, P and Ti. Although both types of the Sanshui lavas have rather uniform Nd isotope compositions [_Nd(T) ≈ +6 to +4]that are comparable to Late Cenozoic basalts around the South China Sea, the felsic rocks possess apparently higher initial Sr isotope ratios (I_Sr up to 0.713) and form a horizontal array to the right in the Nd vs. Sr isotope plot. Closed system differentiation of mantle-derived magmas in a ‘double diffusive’ magma chamber is considered for the bimodal volcanism, in which the trachytes and rhyolites represent A-type melts after extensive crystal fractionation in the upper portion of the chamber. Such A-type melts were later contaminated by small amounts (1–3%) of upper crustal materials during ascent. On the other hand, composition of lavas in the other two basins varies from tholeiitic basalt to andesite. Their Sr and Nd isotope ratios [I_Sr ≈ 0.705 to 0.711; _Nd(T) ≈ +1 to − 5] and generally correlative Nb-Ta depletions suggest a distinct magma chamber process involving fractional crystallization concomitant with assimilation of the country rock. We conclude that these Paleogene volcanic activities resulted from the lithospheric extension in south China that migrated southwards and eventually led to opening of the South China Sea during 30-16 Ma.     

Origins of Nd–Sr–Pb isotopic variations in single scheelite grains from Archaean gold deposits,Western Australia

Accessory gangue scheelite (CaWO₄) from the Archaean Mt. Charlotte lode Au deposit can be divided into two types with different rare earth element (REE) signatures. In some scheelite grains, specific REE signatures are reflected by different cathodoluminescence colours, which can be used to map their often complex oscillatory intergrowths. Domains with specific REE contents from two grains were sampled for Sm/Nd, Rb/Sr and Pb isotopic analyses using a micro-drilling technique.Type I scheelite is strongly enriched in middle REE (MREE) and Eu anomalies are either absent or slightly positive. Four fragments collected from Type I regions of two crystals have initial ⁸⁷Sr/⁸⁶Sr and ε_Nd values ranging from 0.70141 to 0.70163 and +2.5 to +3.5, respectively, and Pb isotope ratios reflecting the composition of greenstone sequence. This may indicate that Nd and Pb have their source, either locally or regionally, in the greenstones. Basic greenstone lithologies have ⁸⁷Sr/⁸⁶Sr<0.7015, and the radiogenic Sr signatures indicate that part of the Sr originated from felsic lithologies located either within or beneath the host greenstone pile. Alternatively, the Sr signature may have evolved from preferential leaching of a Rb-rich mineral during hydrothermal alteration of the greenstone.The REE patterns of Type II scheelite are either flat or MREE-depleted and have strong positive Eu anomalies. Three fragments collected from Type II regions of the same two crystals have initial ⁸⁷Sr/⁸⁶Sr ratios and ε_Nd values between 0.70130 and 0.70146, and +1.1 to +2.6, respectively, and Pb isotope signatures that are once again similar to that of the greenstone. This implies that ⁸⁷Sr/⁸⁶Sr ratios in Type II fluids were closer to those of the host dolerite (0.7008–0.7013), due to more extensive fluid interaction with the dolerite.A positive correlation between Na and REE suggests that REE³⁺ are accommodated by the coupled substitution REE³⁺+Na⁺=2 Ca²⁺ into both Type I and Type II scheelite. This is consistent with a fractional crystallisation model to explain the change in REE patterns from Type I to Type II, but not with a model involving different coupled substitutions and fluids from different origins. We propose that the complex REE and isotopic signatures of scheelite at Mt. Charlotte are related to small (<m) to medium (<km) scale processes involving mixing between “fresh” batches of hydrothermal fluid with fluids that had already been involved in extensive wall-rock alteration.The very high-ε_Nd values measured in some scheelites have been previously used to link gold mineralisation with komatiites containing unusually high Sm/Nd ratios. However, tiny (<20 μm) grains of secondary hydroxyl-bastnäsite were found within micro-fractures of one scheelite grain containing an extremely high-ε_Nd signature. The hydroxyl-bastnäsite probably formed during recent REE redistribution within the scheelite as a result of meteoric fluid circulation. The scale of this cryptic low-temperature alteration is sufficient to explain the anomalously high-ε_Ndi values observed in scheelite from Western Australia.     

河北承德盆地114 Ma大北沟组玄武岩地球化学及其对华北克拉通岩石圈地幔减薄作用的制约

华北克拉通罕见年龄界于120～100Ma的火山岩。承德盆地大北沟组火山岩下部主要由柱状节理橄榄玄武岩组成,中上部主要由安山岩组成。对紧邻玄武岩的上覆安山岩的火山锆石U-PbLA-ICPMS定年结果表明,形成年龄为(113.6±0.87)Ma,代表了该套火山岩的喷发年龄,表明它们形成于早白垩世晚期。对3件玄武岩样品的分析结果表明,它们亏损高场强元素(Nb、Ta、Zr、Hf),初始87Sr/86Sr同位素比值为0.7059,εNd(114Ma)为-11.04,具有富集型岩石圈地幔的特征。但该套玄武岩的主量和微量元素特征则介于华北克拉通中生代年龄>120Ma具古老富集型地幔特征的玄武岩和年龄<100Ma具亏损软流圈性质的玄武岩之间,表明113.6Ma时华北克拉通岩石圈地幔在元素组成方面已具有由富集地幔向亏损型软流圈地幔转变的特征。大北沟组玄武岩的地球化学特征表明,114Ma时华北克拉通岩石圈地幔已减薄。     

雅鲁藏布江缝合带西段东波蛇绿岩OIB型玄武岩的厘定及其形成环境

雅鲁藏布江缝合带(YZSZ)西段分为两支,南带蛇绿岩的成因对整个缝合带的性质和构造背景的探讨起到十分关键作用,但由于地区偏远、交通不便,研究程度一直十分薄弱.本文报道了南带的东波蛇绿岩中洋岛型玄武岩及有关沉积岩的发现和成因探讨.东波蛇绿岩主要由地幔橄榄岩(方辉橄榄岩、含单辉方辉橄榄岩和透镜状纯橄岩)和上覆火山-沉积岩组成,未见堆晶岩和枕状熔岩等典型洋壳端元.火山-沉积岩盖层为一套稳定的海相层序,主要由硅质灰岩、红色硅质岩等沉积岩和玄武岩和玄武火山碎屑岩组成.OIB型玄武岩的特征表现为低SiO2和MgO,高TiO2、P2O5和(K2O+Na2O),富集Nb、Ta,亏损Th、K、Pb、Sr.微量元素和Sr、Nd、Pb同位素数据显示,该玄武质源区来自石榴石尖晶石二辉橄榄岩2％ ～ 5％的部分熔融.成分研究显示,硅质岩形成于大陆边缘环境,为洋岛或海山和大陆边缘物质在生物作用下形成的.以上证据表明,东波火山-沉积岩层序具有典型海山特征,与世界上典型的地幔柱型蛇绿岩可对比,属于地幔柱热点活动的产物.因此,可以认为,地幔柱热点在与冈瓦纳大陆北缘岩石圈地幔相互作用过程中,不但促使YZSZ西段南带(达巴-休古嘎布)特提斯洋盆打开,还可能与YZSZ蛇绿岩中普遍包含金刚石等异常地幔矿物群有直接的动力学关系.     

Rb–Sr and Sm–Nd isotope systematics and geochemical studies on metavolcanic rocks from Peddavura greenstone belt: Evidence for presence of Mesoarchean continental crust in easternmost part of Dharwar Craton,India

Linear, north–south trending Peddavura greenstone belt occurs in easternmost part of the Dharwar Craton. It consists of pillowed basalts, basaltic andesites, andesites (BBA) and rhyolites interlayered with ferruginous chert that were formed under submarine condition. Rhyolites were divided into type-I and II based on their REE abundances and HREE fractionation. Rb–Sr and Sm–Nd isotope studies were carried out on the rock types to understand the evolution of the Dharwar Craton. Due to source heterogeneity Sm–Nd isotope system has not yielded any precise age. Rb–Sr whole-rock isochron age of 2551 ± 19 (MSWD = 1.16) Ma for BBA group could represent time of seafloor metamorphism after the formation of basaltic rocks. Magmas representing BBA group of samples do not show evidence for crustal contamination while magmas representing type-II rhyolites had undergone variable extents of assimilation of Mesoarchean continental crust (>3.3 Ga) as evident from their initial ε _Nd isotope values. Trace element and Nd isotope characteristics of type I rhyolites are consistent with model of generation of their magmas by partial melting of mixed sources consisting of basalt and oceanic sediments with continental crustal components. Thus this study shows evidence for presence of Mesoarchean continental crust in Peddavura area in eastern part of Dharwar Craton.     

Nd and Sr isotope study of hydrothermal scheelite and host rocks at Omai, Guiana Shield: implications for ore fluid source and flow path during the formation of orogenic gold deposits

Omai is a high tonnage, low-grade, world-class gold deposit located in the Paleoproterozoic Guiana Shield. It is the second most important gold deposit in the Guiana Shield (after Las Cristinas, Venezuela), and one of the largest in South America (4.0 million oz.). Sm-Nd and Sr isotope data are presented for host rocks and for scheelite from auriferous quartz-carbonate-scheelite-sulfide-telluride veins from the Omai deposit. Gold-bearing veins are hosted by the Paleoproterozoic Barama-Mazaruni Supergroup, a greenstone belt sequence consisting of mafic volcanic rocks interbedded with sedimentary rocks that are intruded by quartz-feldspar porphyry and rhyolite dikes. This lithologic sequence was folded and metamorphosed to lower greenschist facies during the Paleoproterozoic Trans-Amazonian orogeny. The volcano-sedimentary unit was intruded by a post-tectonic quartz monzodiorite-diorite-hornblendite stock. Initial Nd isotope ratios for the Omai volcanic rocks range from ɛ_Nd=+2.1 to +4.2. These values suggest that this part of the Guiana Shield was a site of new crust formation during the Paleoproterozoic and was not contaminated by older (Archean), reworked continental crust. Initial Nd isotope ratios for the Omai stock range between +0.5 and +2.3, which suggest limited contamination with previously formed continental crust. Although the Nd isotopic ratios of gold-related scheelites overlap with those of the host rocks, particularly the tholeiitic basalts at the interpreted time of vein emplacement, the lack of both isotopic mixing and significant Nd movement during the hydrothermal process suggest that the Nd isotope composition can be used to determine the isotopic characteristics of the ore fluid source area. At Omai, the ore fluid is largely derived from a radiogenic Nd source, represented by mantle or lower crustal reservoirs. Strontium isotope ratios for the scheelites cluster tightly between 0.7019 and 0.7021. The Sr isotope data suggest that unlike Nd, Sr was significantly mobile during the hydrothermal process. The fluids responsible for the Omai deposit may have picked up Sr along the flow path. The constant low Sr isotope values of scheelites probably reflect the key role that the local tholeiitic basalts played as the main source of Sr in the fluids. Whereas Nd isotopes identify the fluid source area, the Sr isotopes map the fluid flow paths. Received: 11 February 1999 / Accepted: 1 November 1999     

Fluid flow in subduction zones: evidence from Nd- and Sr-isotope variations in metabasalts of the Franciscan complex,California

Greenstone, blueschist and eclogite metabasaltic blocks from the Franciscan complex of California preserve extensive petrographic and chemical evidence for interaction with hydrous fluids at high-P, low-T metamorphic conditions. The Nd and Sr isotope variations within and among the blocks constrain the origin of the basaltic protoliths, the nature of the fluid metasomatism that occurred within the upper levels (15–45 km) of the paleosubduction zonc, and the character and provenance of the rock that generated the hydrous fluids within the paleosubduction zone. Samples with little or no petrographic evidence of retrograde alteration and unaltered garnet separates have _Nd. With increasing degrees of retrograde alteration, Nd isotope compositions are consistently lower, ranging down to _Nd(160)=5. Actinolitic alteration rinds which are present on some blocks have the least radiogenic compositions with _Nd=1.6 to 6.1. While Nd isotope compositions of unaltered blockes are in the range expected for basalt derived from normal depleted mantle, the Sr isotope compositions are more radiogenic ranging from _Sr(160)=–5 to +11. Compositions of unaltered eclogite and blue-schist blocks are consistent with a protolith origin in normal oceanic crust derived from depleted mantle. The Sr isotopy systematics indicate that the protoliths were modified by seawater alteration in an ocean-floor hydrothermal system. Isotopic compositions of samples from parts of blocks that have a retrograde metamorphic overprint show a strong correlation between less radiogenic Nd compositions and the extent of retrograde metamorphism. Maximum Nd isotope ratios of the metasomatizing fluid are provided by analyses of actinolitic rinds, and range from _Nd(160)=1.6 to 6.1. A possible source for fluids of this composition is subducted sediment that was derived from a continental craton. Because rind formation occurred while the basaltic blocks were within an ultramafic matrix, the fluids must have migrated from sediments in the accretionary wedge into an overlying wedge of mantle material imbricated with blocks of oceanic crust. This suggests possibly km-scale movement of fluids that carry an amount of the rare-earth elements sufficient to significantly modify the trace-element budget of subducted basalt.     

A Study of REE and Pb,Sr and Nd Isotopes in Garnet—Lherzolite Xenoliths from Mingxi,Fujian Province

The REE and Pb, Sr, Nd isotopes in three xenoliths from limburgite and scoria-breccias, including spinel-lherzolite, spinel-garnet-lherzolite and phlogopite-gamet-lherzolite, were analysed. The REE contents of the xenoliths are 1.3 to 3.3 times those of the chondrites with their REE patterns characterized by weak LREE depletion. The¹⁴³Nd/¹⁴⁴Nd values of whole rocks and minerals range from 0.51306 to 0.51345 with εNd=+ 8.2− +15.8,²⁰⁶Pb/²⁰⁴ Pb < 18.673, and²⁰⁷Pb/²⁰⁴Pb < 15.574. All this goes to show that the upper mantle in Mingxi at the depth of 67–82 km is a depleted mantle of MORB type, with⁸⁷Sr/⁸⁶ Sr ratios 0.70237–0.70390. In Nd-Sr diagram the data points of whole rocks are all out of the mantle array, implying that the xenoliths from Mingxi have more radiogenic Sr isotopes than those of the mantle array.