Polymetamorphism of the Variscan Basement of the Moldanubian Black Forest （Germany） Documented in Zircon and Garnet Minerals from Gneisses

High-grade metamorphic Variscan basement is exposed in the Moldanubian zone of the Black Forest (BF), being the internal zone of the European Variscan belt. Zircon grains from K-rich felsic orthogneisses and an anatectic paragneiss in the Moldanubian Black Forest demonstrate a multi-stage crystallization at ～ 600 Ma, ～ 480 Ma, ～ 400 - 380 Ma, and ～350 Ma. The last three stages of crystallization probably represent metamorphic overprint during pre-Variscan and Variscan metamorphism.Using stepwise leaching procedures, garnet minerals from felsic orthogneisses as well as paragneisses in the Moldanubian Black Forest yielded Early Carboniferous Sm-Nd ages (～ 330- 340 Ma), which are consistent with the well-constrained Variscan HT metamorphic event,and Early Palaeozoic ( ～480 Ma) to Devonian ( ～400 - 370 Ma) Pb-Pb ages. The coincidence of growth time for zircon and garnet minerals at Early Palaeozoic is interpreted as dating a metamorphic event. These garnet data demonstrate that the Moldanubian BF basement underwent at least two metamorphic events during the Early Palaeozoic and Early Carboniferous.During the Variscan HT metamorphism, the Sm-Nd system of garnet was disturbed, but not the U-Pb system, implying the peak metamorphic temperature was lower than ～800℃.     

Zircon ages and Nd isotopic and chemical compositions of orthogneisses from the Black Forest, Germany: evidence for a Cambrian magmatic arc

 Single zircon U–Pb dating combined with ²⁰⁷Pb/²⁰⁶Pb ages obtained by the evaporation method constrains the emplacement of tonalitic, trondhjemitic, and granodioritic orthogneisses of the Moldanubian zone in the Black Forest between 500 and 510 Ma. Two detrital zircon populations of 1.9 and 1.6 Ga indicate Early-Middle Proterozoic material in the former setting of the basement. The initial e_Nd values range from –0.1 to –3.4 and mean crustal residence ages of 1.0–1.4 Ga are consistent with involvement of Early-Middle Proterozoic crust, and a subordinate juvenile component probably originating from subduction-related melting of the mantle. The orthogneisses have fractionated REE patterns and slightly higher K₂O/Na₂O ratios than typical low-K tonalite–trondhjemite–granite suites. The chemical data are interpreted as evidence for melting of amphibolite and contributions from evolved crust. The emplacement of the orthogneisses was superceded by a high-temperature metamorphic event at ∼480 Ma which we interpret as a result of lithospheric thinning in a marginal basin behind a Cambrian magmatic arc. Received: 29 March 1999 / Accepted: 25 August 1999     

The Aguablanca Cu–Ni ore deposit (Extremadura, Spain), a case of synorogenic orthomagmatic mineralization: age and isotope composition of magmas (Sr, Nd) and ore (S)

The Aguablanca Cu–Ni orthomagmatic ore deposit is hosted by mafic and ultramafic rocks of the Aguablanca stock, which is part of the larger, high-K calc-alkaline Santa Olalla plutonic complex. This intrusive complex, ca. 338 Ma in age, is located in the Ossa-Morena Zone (OMZ) of the Iberian Variscan Belt. Mineralization consists mainly of pyrrhotite, pentlandite and chalcopyrite resulting from the crystallization of an immiscible sulphide-rich liquid. Isotope work on the host igneous rocks (Sr, Nd) and the ore (S) suggests that contamination with an upper-crustal component took place at some depth before final emplacement of the plutons (Nd₃₃₈=−6 to −7.5; Sr₍₃₃₈₎=0.7082 to 0.7100; δ³⁴S_(sulphides) near +7.4‰). Assimilation–fractional crystallization (AFC) processes are invoked to explain early cumulates and immiscible sulphide-magma formation. Intrusion took place at the beginning of the type-A oblique subduction of the South Portuguese Zone under the Ossa-Morena Zone and was probably driven by transpressive structures (strike-slip faults). The mineralization is thus synorogenic.Aguablanca is probably the first case referred to in the literature of a magmatic Cu–Ni ore deposit hosted by calc-alkaline igneous rocks.     

Petrogenesis of rhyolites and trachytes from the Deccan Trap: Sr,Nd and Pb isotope and trace element evidence

Trachytes and rhyolites from Salsette Island, north of Bombay, have distinctive trace element and isotope features which mark them out from typical crustal melts. Their highly incompatible trace element and Sr-, Nd and Pb isotope ratios are similar to those of the associated Deccan flood basalts. Thus the rhyolites and trachytes are closely related to the basalts, and a striking compositional gap between 50 and 65% SiO₂ suggests that the high SiO₂ rocks evolved by 10–15% partial melting followed by variable amounts of fractional crystallisation. The source material could have been basalt within the Deccan Trap, or related gabbroic rocks in deep crustal sill complexes. The rhyolites yield an Rb-Sr whole rock age of 61.5±1.9 Ma, with a slightly high initial ⁸⁷Sr/⁸⁶Sr=0.7085±18. It is argued that crustal extension provides a suitable regime for the generation of acid magmas by partial melting of associated basic rocks.     

北苏鲁仰口地区变辉长岩中锆石U-Pb定年、微量元素和Hf同位素特征及其地质意义

北苏鲁仰口地区出露超高压的变辉长岩.锆石阴极发光图像和其内部矿物包体激光拉曼测试的联合研究结果表明,变辉长岩锆石具有弱发光效应的岩浆韵律环带的核和被改造的强发光效应的边.岩浆韵律环带的核部保存大量而复杂的矿物包体,包括普通辉石(Cpx)+斜方辉石(Opx)+斜长石(P1)+石英(Qtz)+黑云母(Bt)+钛铁矿(Ilm)+磷灰石(Ap);边部保存的矿物包体则相对较少,包括普通辉石(Cpx)+斜方辉石(Opx)+斜长石(Pl)+磷灰石(Ap).尽管岩浆韵律环带核部的稀土元素总合量比被改造的锆石边部明显偏高,但二者稀土元素配分模式具有明显的相似性,主要表现为轻稀土相对亏损,而重稀土明显富集,相应的(La/Yb)N=0.00015～0.00039,并具有明显的负Eu异常(Eu/Eu*=0.20～0.26)、相对明显的正Ce异常(Ce/Ce*=71.5～147.4)和较高的Th/U比值(1.97～2.69).上述特征表明,仰口地区变辉长岩中的锆石均为继承性的岩浆锆石,而没有新生的变质锆石.LA-(MC)-ICP-MS锆石原位U-Pb定年和Lu-Hf同位素分析结果表明,两件锆石样品Y1和Y2的年龄数据所构成的不一致线显示了十分接近的上交点和下交点年龄.其上交点年龄分别为785±15Ma(2σ)和784±12Ma(2σ),应代表原岩的形成时代,表明变辉长岩的原岩与Rodinia超大陆裂解的岩浆事件存在密切的成因关系;而下交点年龄分别为226±24Ma(2σ)和228±26Ma(2σ),与苏鲁其它类型超高压岩石中含柯石英锆石微区记录的变质年龄十分吻合,应代表变辉长岩的超高压变质时代.岩浆结晶锆石的核部具有明显偏高的176Lu/177Hf(0.00044～0.00291)和176Yh/177Hf(0.0165～0.1168)比值,而176Hf/177Hf比值变化于0.281956～0.282048之间,相应的εHf(t)=-8.5～-14.0,tDM2=2.03～2.32Ga,表明仰口地区变辉长岩的原岩起源于古元古代时期的富集地幔或发生部分熔融的下地壳残留体.被改造的岩浆结晶锆石的边部则具有明显偏低的176Lu/177Hf(0.00029～0.00060)和176Yh/177Hf(0.0112～0.0200)比值,而176Hf/177Hf(t)比值变化于0.281953～0.282002之间,相应的εHf(t)=-10.2～-11.9,tDM2=2.12～2.21Ga.与岩浆结晶锆石核部相比,被改造的岩浆锆石边部的176Lu/177Hf、176Yb/177Hf、176Hf/177Hf(t)比值和εHf(t)和tDM2值的变化范围更小,表明中-新三叠纪的超高压变质作用使岩浆结晶锆石边部的Lu-Hf同位素体系发生调整,更趋向于均一化.     

Post-collisional melting of crustal sources: constraints from geochronology,petrology and Sr,Nd isotope geochemistry of the Variscan Sichevita and Poniasca granitoid plutons (South Carpathians,Romania)

The Sichevita and Poniasca plutons belong to an alignment of granites cutting across the metamorphic basement of the Getic Nappe in the South Carpathians. The present work provides SHRIMP age data for the zircon population from a Poniasca biotite diorite and geochemical analyses (major and trace elements, Sr–Nd isotopes) of representative rock types from the two intrusions grading from biotite diorite to biotite K-feldspar porphyritic monzogranite. U–Pb zircon data yielded 311 ± 2 Ma for the intrusion of the biotite diorite. Granites are mostly high-K leucogranites, and biotite diorites are magnesian, and calcic to calc-alkaline. Sr, and Nd isotope and trace element data (REE, Th, Ta, Cr, Ba and Rb) permit distinguishing five different groups of rocks corresponding to several magma batches: the Poniasca biotite diorite (P₁) shows a clear crustal character while the Poniasca granite (P₂) is more juvenile. Conversely, Sichevita biotite diorite (S₁), and a granite (S₂*) are more juvenile than the other Sichevita granites (S₂). Geochemical modelling of major elements and REE suggests that fractional crystallization can account for variations within P₁ and S₁ groups. Dehydration melting of a number of protoliths may be the source of these magma batches. The Variscan basement, a subduction accretion wedge, could correspond to such a heterogeneous source. The intrusion of the Sichevita–Poniasca plutons took place in the final stages of the Variscan orogeny, as is the case for a series of European granites around 310 Ma ago, especially in Bulgaria and in Iberia, no Alleghenian granitoids (late Carboniferous—early Permian times) being known in the Getic nappe. The geodynamical environment of Sichevita–Poniasca was typically post-collisional of the Variscan orogenic phase.     

Sr,Nd,Pb and trace element systematics of the New Caledonia harzburgites:Tracking source depletion and contamination processes in a SSZ setting

The New Caledonia ophiolite(Peridotite Nappe)consists primarily of harzburgites,locally overlain by mafic-ultramafic cumulates,and minor spinel and plagioclase lherzolites.In this study,a comprehensive geochemical data set(major and trace element,Sr-Nd-Pb isotopes)has been obtained on a new set of fresh harzburgites in order to track the processes recorded by this mantle section and its evolution.The studied harzburgites are low-strain tectonites showing porphyroclastic textures,locally grading into protomylonitic textures.They exhibit a refractory nature,as attested by the notable absence of primary clinopyroxene,very high Fo content of olivine(91-93 mol.%),high Mg#of orthopyroxene(0.91-0.93)and high Cr#of spinel(0.44-0.71).The harzburgites are characterised by remarkably low REE concentrations(<0.1 chondritic values)and display"U-shaped"profiles,with steeply sloping HREE(DyN/YbN=0.07-0.16)and fractionated LREE-MREE segments(LaN/SmN=2.1-8.3),in the range of modern fore-arc peridotites.Geochemical modelling shows that the HREE composition of the harzburgites can be reproduced by multi-stage melting including a first phase of melt depletion in dry conditions(15%fractional melting),followed by hydrous melting in a subduction zone setting(up to 15%-18%).However,melting models fail to explain the enrichments observed for some FME(i.e.Ba,Sr,Pb),LREE-MREE and Zr-Hf.These enrichments,coupled with the frequent occurrence of thin,undeformed films of Al2 O3,and CaO-poor orthopyroxene(Al2O3=0.88-1.53 wt.%,CaO=0.31-0.56 wt.%)and clinopyroxene with low Na2 O(0.03-0.16 wt.%),Al2 O3(0.66-1.35 wt.%)and TiO2(0.04-0.10 wt.%)contents,point to FME addition during fluid-assisted melting followed by late stage metasomatism most likely operated by subductionrelated melts with a depleted trace element signature.Nd isotopic ratios range from unradiogenic to radiogenic(-0.80<εNdi≤+13.32)and negatively correlate with Sr isotopes(0.70257≤87Sr/86Sr≤0.70770).Pb isotopes cover a wide range,trending from DMM toward enriched,sediment-like,compositions.We interpret the geochemical signature displayed by the New Caledonia harzburgites as reflecting the evolution of a highly depleted fore-arc mantle wedge variably modified by different fluid and melt inputs during Eocene subduction.     

Rb-Sr and U-Pb isotope studies on migmatites from the Schwarzwald (Germany): constraints on isotopic resetting during Variscan high-temperature metamorphism

Mineral and isotope studies were undertaken on migmatites from the Schwarzwald, Moldanubian zone of the Variscan belt. The aims of the study were to date the migmatite formation and to determine the processes involved in migmatization in order to evaluate their influence on isotopic resetting. Textural evidence and the comparison of mineral compositions from leucosomes and mesosomes of two centimetre-scale migmatite profiles, respectively, suggest that migmatitic textures and mineral assemblages were formed by metamorphic segregation (deformation-enhanced mass transport) rather than by partial melting (anatexis). The results of Rb-Sr thin-slab dating on these profiles indicate that Sr isotopes were not completely reset during migmatization. No true isochron ages, but ages of approximate isotopic homogenization were obtained on the thin slabs by calculating ⁸⁷Sr/⁸⁶Sr ratios back to various stages in their evolution. The coincidence of these Rb-Sr data with U-Pb ages of monazites from migmatites and non-migmatitic gneisses shows that gneisses and migmatites were formed during the same high-temperature event in the Carboniferous (330-335 Ma). The observation that high-temperature metamorphism failed to equilibrate Sr isotopes on the centimetre-scale imposes limitations on the use of conventional whole-rock isochron techniques in dating migmatites.     

Genesis of post-collisional granitoids and basement nature of the Junggar Terrane, NW China: Nd–Sr isotope and trace element evidence

The post-collisional magmatism of the Junggar Terrane is characterized by intrusion of large amounts of granitoids and minor basic/ultrabasic rocks. The granitoids comprise two magmatic suites: calc-alkaline and alkaline, which were emplaced contemporaneously at about 294 Ma. The calc-alkaline rocks are typically sodium-rich (Na₂O/K₂O=1.1–3.5) and metaluminous (A/NK >1.0, A/CNK=0.78–1.04). They show mildly fractionated REE patterns ((La/Yb)_N<15) and spidergrams with strong depletion of Nb, Ti and, to a lesser extent, Sr. The alkaline granites have high contents of SiO₂ (75–78%), alkalis, Nb, HREE, Y, Sn, F and high FeO/MgO ratios and huge Sr and Eu depletion in the spidergrams. Moreover, they display characteristic tetrad REE patterns and non-CHARAC trace element behaviour. The two rock suites have similar initial Nd and Sr isotopic compositions, with _Nd(T) in the range +5.2 to +7.1 and I_Sr mostly in the range 0.7031–0.7041. This points to a predominance of juvenile components in their sources. The calc-alkaline rocks are most probably derived by dehydration-melting of a basic lower crust leaving behind a granulite residue. The process was probably triggered by underplating of mantle-derived basic magmas in an extensional regime. The alkaline granites are considered to have formed by differentiation of the calc-alkaline granitoids. Our study argues for a juvenile continental crust for the basement of the Junggar terrane, which is likely dominated by early Paleozoic oceanic crust and arc complex that were deeply buried during the late Paleozoic subduction and accretion.     

Strain partitioning and preservation of Ar/Ar ages during Variscan exhumation of a subducted crust (Malpica–Tui complex, NW Spain)

The Malpica–Tui complex (NW Iberian Massif) consists of a Lower Continental Unit of variably deformed and recrystallized granitoids, metasediments and sparse metabasites, overridden by an upper unit with rocks of oceanic affinities. Metamorphic minerals dated by the ⁴⁰Ar/³⁹Ar method record a coherent temporal history of progressive deformation during Variscan metamorphism and exhumation. The earliest stages of deformation (D1) under high-pressure conditions are recorded in phengitic white micas from eclogite-facies rocks at 365–370 Ma. Following this eclogite-facies peak-metamorphism, the continental slab became attached to the overriding plate at deep-crustal levels at ca. 340–350 Ma (D2). Exhumation was accompanied by pervasive deformation (D3) within the continental slab at ca. 330 Ma and major deformation (D4) in the underlying para-autochthon at 315–325 Ma. Final tectonothermal evolution included late folding, localized shearing and granitic intrusions at 280–310 Ma.

Dating of high-pressure rocks by the ⁴⁰Ar/³⁹Ar method yields ages that are synchronous with published Rb–Sr and Sm–Nd ages obtained for both the Malpica–Tui complex and its correlative, the Champtoceaux complex in the French Armorican Massif. The results indicate that phengitic white mica retains its radiogenic argon despite been subjected to relatively high temperatures (500–600 °C) for a period of 20–30 My corresponding to the time-span from the static, eclogite-facies M1 peak-metamorphism through D1-M2 eclogite-facies deformation to amphibolite-facies D2-M3. Our study provides additional evidence that under certain geological conditions (i.e., strain partitioning, fluid deficiency) argon isotope mobility is limited at high temperatures, and that ⁴⁰Ar/³⁹Ar geochronology can be a reliable method for dating high pressure metamorphism.     

华北克拉通北部古-中元古代富碱侵入岩的Nd、Sr、Pb同位素地球化学：岩石圈地幔富集的证据

华北克拉通北部古-中元古代富碱侵入岩主要分布在燕辽三叉裂堑系和辽吉拗拉谷中及附近,为一套高碱高钾的基性-中性岩,以正长岩类为主。本文通过开展系统的 Nd、Sr、Pb 同位素研究,发现所有岩体岩石均以高负ε_(Nd)(t)为特征,ε_(Nd)(t)=-3.4～-7.5,平均值为～4.8,这与研究区古-中元古代基性-超基性岩石的 Nd 同位素特征(ε_(Nd)(t)=-4～-8) 一致,与燕辽裂堑系发育的偏碱性火山岩 Nd 同位素特征(ε_(Nd)(t)=-4.3～-8.9)也比较相似,表明它们的物质来源相似,都与富集地幔有关。Sr 同位素初始比值(~(87)St/~(86)Sr)_i比较低,主要变化在0.7028～0.7053之间,平均值为0.7041。钾长石铅同位素组成普遍较低,~(206)Pb/~(204)Pb、~(207)pb/~(204)Pb、~(208)Pb/~(204)Pb 比值变化范围(梁屯-矿洞沟岩体除外)分别为14.500～15.70l、14.887～15.150和34.178～36.537,平均值分别为14.968、14.984和35.057。在ε_(Nd)(t)-ε_(Sr)(t)图解上,所有岩体的投影点均在地幔演化趋势线附近,比较接近 EMI 型富集地幔端员,暗示它们的物质来源与 EMI 型富集地幔有关;钾长石 Pb 同位素模式图也说明这些岩体物质来源与地幔和下地壳有关。通过两端员混合模拟,揭示了岩浆演化过程中存在少量的下地壳物质混染,平均约14%左右。从2.5Ga 左右开始华北克拉通岩石圈地幔的亏损程度逐渐变小,在2.2Ga 左右局部呈现富集性特征,1.85Ga时整个岩石圈地幔已经完全转变为富集性,之后富集程度越来越高。推测早期俯冲携带的壳源物质以及后期地幔流体的交代作用可能是岩石圈地幔逐渐转变为富集性的原因。     

Zircon U-Pb age,trace element and Hf isotope composition of Sepon Au-Cu deposit,Laos: tectonic and metallogenic implications

The Truong Son Fold Belt, located at the northeastern margin of the Indochina Block, is considered to be tectonically linked to the subduction of the Paleotethys Ocean and subsequent collision. Sepon is one of the most important super large deposits of the Truong Son Fold Belt. Our LA-ICP-MS zircon U-Pb dating results show that granodiorite porphyry samples from the Sepon deposit have ages of 302.1±2.9 Ma, which is a crucial phase for magmatic-tectonical activities from the Late Carboniferous to Early Permian and has avital influence on the mineralization of copper and gold. Zircon from granodiorite porphyry yields ε_Hf (t) values of 4.32 to 9.64, and T_DM2 has an average age of 914 Ma, suggesting that the source of the granodiorite porphyry in the region were mainly mantle components but underwent mixing and contamination of crust materials. The Ce⁴⁺/Ce³⁺ value of zircon in the granodiorite porphyry varys greatly from 2.4 to 1438.29, which shows magma mixing might occur. Considering the characteristics of trace elements in the zircon and the whole rock geochemical characteristics of intrusion rocks as well as the characteristics of regional volcanic-sedimentary association, it is indicated that the tectonic setting may be the continental arc environment. The Sepon Au-Cu deposit is derived from emplacement of calc-alkaline intermediate-acid magma with coming from deep sources in the subduction process of the Paleotethys Ocean, forming porphyry Mo-Cu, skarn Cu-Au mineralization and a hydrothermal sedimentary-hosted Au mineralization in the wall rocks.     

Tracking meteoric infiltration into a magmatic-hydrothermal system: A cathodoluminescence, oxygen isotope and trace element study of quartz from Mt. Leyshon, Australia

The oxygen isotope and trace element composition of hydrothermal quartz has been integrated with scanning electron microscope-cathodoluminescence (SEM-CL) images and fluid inclusion properties to track fluid sources and hydrothermal processes in the Mt. Leyshon Au deposit, Australia. Oxygen isotope and trace element data were collected on parallel traverses across the same quartz sections, using secondary isotope mass spectrometry (SIMS) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), respectively, with SEM-CL images obtained before analysis for petrographic context. Over the 280 to 650 °C quartz precipitation range suggested by fluid inclusion microthermometry, δ¹⁸O_quartz varies from 0.0 to 14.4‰, corresponding to a wide range of equilibrium δ¹⁸O_fluid values, from-6.1 to 10.2‰ (vs. V-SMOW). The δ¹⁸O_quartz signature varies systematically among distinct SEM-CL quartz generations (both within and between samples), and can be correlated with variations in temperature and fluid composition, but is independent of intra-generational oscillatory zoning. In contrast, Al and Li concentrations correlate broadly with CL intensity in oscillatory quartz, whereas their concentration is unpredictable in sealed fractures and overgrowths. Concentrations of B, Mg, Na, P, Cl, K, Ti, Mn, Fe, Ge, and Sn are independent of Al, Li, and oscillatory CL features, but Ti correlates with quartz precipitation temperature. Although no systematic correlation between δ¹⁸O_quartz and trace element concentrations was found, complementary patterns exist in narrow overgrowths of low δ¹⁸O_quartz ( 0‰) and high Al (> 10,000 ppma). These quartz zones likely formed during the incursion of ¹⁸O-depleted meteoric water into the magmatically-dominated Mt. Leyshon hydrothermal system. We interpret the highest Al concentrations as the result of high quartz precipitation rates, triggered by depressurisation of the hydrothermal cell. The decoupling of oxygen isotope and trace element patterns in quartz leads to the suggestion that (1) under most circumstances, temperature and fluid chemistry dominate δ¹⁸O_quartz, and (2) the trace element record, and in particular Al and Li, is influenced by the superimposed effects of quartz precipitation rate.     

Volatile (S,Cl and F) and fluid mobile trace element compositions in melt inclusions: implications for variable fluid sources across the Kamchatka arc

Volatile element, major and trace element compositions were measured in glass inclusions in olivine from samples across the Kamchatka arc. Glasses were analyzed in reheated melt inclusions by electron microprobe for major elements, S and Cl, trace elements and F were determined by SIMS. Volatile element–trace element ratios correlated with fluid-mobile elements (B, Li) suggesting successive changes and three distinct fluid compositions with increasing slab depth. The Eastern Volcanic arc Front (EVF) was dominated by fluid highly enriched in B, Cl and chalcophile elements and also LILE (U, Th, Ba, Pb), F, S and LREE (La, Ce). This arc-front fluid contributed less to magmas from the central volcanic zone and was not involved in back arc magmatism. The Central Kamchatka Depression (CKD) was dominated by a second fluid enriched in S and U, showing the highest S/K₂O and U/Th ratios. Additionally this fluid was unusually enriched in ⁸⁷Sr and ¹⁸O. In the back arc Sredinny Ridge (SR) a third fluid was observed, highly enriched in F, Li, and Be as well as LILE and LREE. We argue from the decoupling of B and Li that dehydration of different water-rich minerals at different depths explains the presence of different fluids across the Kamchatka arc. In the arc front, fluids were derived from amphibole and serpentine dehydration and probably were water-rich, low in silica and high in B, LILE, sulfur and chlorine. Large amounts of water produced high degrees of melting below the EVF and CKD. Fluids below the CKD were released at a depth between 100 and 200 km due to dehydration of lawsonite and phengite and probably were poorer in water and richer in silica. Fluids released at high pressure conditions below the back arc (SR) probably were much denser and dissolved significant amounts of silicate minerals, and potentially carried high amounts of LILE and HFSE. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Major and trace element geochemistry and isotope (Sr, Nd, Pb, O) systematics of an Archaean basement involved in a 2.0 Ga very high-temperature (1000°C) metamorphic event: In Ouzzal Massif, Hoggar, Algeria

The In Ouzzal granulitic massif is composed mainly of various meta-igneous rocks which, in spite of Rb, U, Th, Cs and some K and Sr mobility, can be dated and generally classified according to their chemical composition as follows. Basic and ultrabasic granulites interlayered with the metasediments correspond to (1) ultrabasic cumulates from dislocated tholeiitic bodies, (2) ancient komatiitic to high-Mg tholeiitic basalts similar to the suites found in Archaean greenstone belts and (3) calcalkaline protoliths of high-K andesitic composition. No geochronological constraints are available apart from the depositional age of some associated sediments which is younger than 2.70 Ga detrital zircons, and the Nd model age of the andesitic granulites of c. 3.4 Ga. In spite of the high-grade metamorphism, the acidic magmatic precursors of the charnockites can be divided in three groups. (1) The most juvenile acid orthogneisses are trondhjemitic or tonalitic in composition, being similar to the TTG suites which are classically considered to be formed by partial melting of mantle-derived protoliths. The 3.3–3.2 Ga T_DM indicates a possible age of separation from the mantle reservoir while the plutons may have been emplaced between 3.3 and 2.7 Ga (U–Pb zircon & Nd ages). (2) A group of alkaline granitic gneisses, similar in composition to rift-related-granites, were emplaced at 2650±10 Ma (U–Pb & Rb–Sr ages) in a thick continental crust. (3) Calcalkaline granodioritic and monzogranitic suites derived from the partial melting of continental precursors (3.5–3.3 Ga), in lower to middle levels of the continental crust. They were emplaced close to 2.5 Ga during crustal thickening. The very high-temperature metamorphism occurred at 2002±7 Ma from the age of synfoliation intrusions and was probably related to major overthrusting. Retrogressive metamorphism is dated at 1.95 Ga from garnet-Nd ages. In spite of the very high-temperature conditions, partial melting during granulite facies metamorphism may be restricted to scarce cordierite-bearing monzogranitic gneisses. The 2.0 Ga VHT metamorphism could be related to overthrusting, extensional or underplating processes.     

Coupled evolution of back-arc and island arc-like mafic crust in the late-Neoproterozoic Agardagh Tes-Chem ophiolite, Central Asia: evidence from trace element and Sr–Nd–Pb isotope data

. We report major-element, trace-element and isotopic data of volcanic rocks from the late-Neoproterozoic (570 Ma) Agardagh Tes-Chem ophiolite in Central Asia, south-west of Lake Baikal (50.5°N, 95°E). The majority of samples are high-alumina basalts and basaltic andesites having island-arc affinities. They were derived from an evolved parental magma (Mg#̾.60, Cr~180 ppm, Ni~95 ppm) by predominantly clinopyroxene fractionation. The parental magma developed from a primary mantle melt by fractionation of about 12% of an olivine+spinel assemblage. The island-arc rocks have high abundances of incompatible trace elements (light rare-earth element abundances up to 100 times chondritic, chondrite-normalised (La/Yb)_n=14.6-5.1) and negative Nb anomalies (Nb/La=0.37-0.62), but low Zr/Nb ratios (7-14). Initial )_Nd values are around +5.5, initial Pb isotopic compositions are ²⁰⁶Pb/²⁰⁴Pb=17.39-18.45, ²⁰⁷Pb/²⁰⁴Pb=15.49-15.61, ²⁰⁸Pb/²⁰⁴Pb=37.06-38.05. Enrichment of large-ion lithophile elements within this group is significant (Ba/La=11-130). Another group of samples consists of back-arc basin-related volcanic rocks. They are most likely derived from the same depleted mantle source as the island-arc rocks, but underwent higher degrees of melting (8-15%) and are not influenced by slab components. They have lower abundances of incompatible trace elements, flat rare-earth element patterns [(La/Yb)_n=0.6-2.4] and higher )_Nd values (+7.8 to +8.5). Negative Nb anomalies are absent (Nb/La=0.81-1.30), but Zr/Nb is high (21-48). At least three components are necessary to explain the geochemical evolution of the volcanic rocks: (1) an enriched (ocean island-like) component characterised by a high Nb concentration (up to 30 ppm), an absent negative Nb anomaly, a low Zr/Nb ratio (~6.5), a low )_Nd value (around 0), and radiogenic ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb; (2) a back-arc basin component similar to N-MORB with a flat rare-earth element pattern and a high )_Nd value (around +8.5); and (3) an island-arc component from a mantle source which was modified by the downgoing slab. Crystal fractionation superimposed on mixing and source contamination by subducted sediments is suitable to explain the observed geochemical data. The most likely geodynamic environment to produce these characteristics is a young, intra-oceanic island-arc system and an associated back-arc basin.     

Genesis of the Bianjiadayuan Pb-Zn polymetallic deposit,Inner Mongolia,China:Constraints from in-situ sulfur isotope and trace element geochemistry of pyrite

The Southern Great Xing'an Range(S(GXR)which forms part of the eastern segment of the Central Asian Orogenic Belt(CAOB)is known as one of the most important Cu-Mo-Pb-Zn-Ag-Au metallogenic belts in China,hosting a number of porphyry Mo(Cu),skarn Fe(Sn),epithermal Au-Ag,and hydrothermal veintype Ag-Pb-Zn ore deposits.Here we investigate the Bianjiadayuan hydrothermal vein-type Ag-Pb-Zn ore deposit in the southern part of the SGXR.Porphyry Sn± Cu± Mo mineralization is also developed to the west of the Ag-Pb-Zn veins in the ore field.We identify a five-stage mineralization process based on field and petrologic studies including(i)the early porphyry mineralization stage,(ii)main porphyry mineralization stage,(iii)transition mineralization stage,(iv)vein-type mineralization stage and(v)late mineralization stage.Pyrite is the predominant sulfide mineral in all stages except in the late mineralization stage,and we identify corresponding four types of pyrites:Pyl is medium-grained subhedral to euhedral occurring in the early barren quartz vein;Py2 is medium-to fine-grained euhedral pyrite mainly coexisting with molybdenite,chalcopyrite,minor sphalerite and galena;Py3 is fine-grained,subhedral to irregular pyrite and displays cataclastic textures with micro-fractures;Py4 occurs as euhedral microcrystals and forms irregularly shaped aggregate with sphalerite and galena.LA-ICP-MS trace element analyses of pyrite show that Cu,Pb,Zn,Ag,Sn,Cd and Sb are partitioned into pyrite as structurally bound metals or mineral micro/nano-inclusions,whereas Co,Ni,As and Se enter the lattice via isomorphism in all types of pyrite.The Cu,Zn,Ag,Cd concentrations gradually increase from Pyl to Py4,which we correlate with cooling and mixing of ore-forming fluid with meteoric water.Py2 contains the highest contents of Co,Ni,Se,Te and Bi,suggesting high temperature conditions for the porphyry mineralization stage.Ratios of Co/Ni(0.03-10.79,average 2.13)and sulphur isotope composition of sulfide indicate typical hydrothermal origin for pyrites.The δ~(34)S_(cDT) values of Pyl(0.42‰-1.61‰,average1.16‰),Py2(-1.23‰to 0.82‰,average 0.35‰),Py3(—0.36‰to 2.47‰average 0.97‰).Py4(2.51‰--3.72‰,average 3.06‰),and other sulfides are consistent with those of typical porphyry deposit(-5‰to 5‰),indicating that the Pb-Zn polymetallic mineralization in the Bianjiadayuan deposit is genetically linked to the Yanshanian(Jurassic-Cretaceous)magmatic-hydrothermal events.Variations of δ~(34) S values are ascribed to the changes in physical and chemical conditions during the evolution and migration of the ore-forming fluid.We propose that the high Sn content of pyrite in the Bianjiadayuan hydrothermal vein-type Pb-Zn polymetallic deposit can be used as a possible pathfinder to prospect for Sn mineralization in the surrounding area or deeper level of the ore field in this region.     

湖南宝山-大坊矿区成矿花岗闪长斑岩的锆石U-Pb年龄、Hf同位素及微量元素组成对区域成矿作用的指示

钦-杭成矿带是华南地区新近识别出的一条重要的中生代斑岩-矽卡岩型铜多金属成矿带。宝山矿床处于铜山岭-宝山-水口山矿区的中部,是湘南地区最大的铜多金属矿床,而大坊金矿床与宝山Cu-Mo-Pb-Zn矿相邻,在空间上亦与花岗闪长斑岩密切相关。矿区内岩浆活动复杂,矿化类型齐全,成矿元素多样。我们对宝山成矿花岗闪长斑岩、花岗闪长质隐爆角砾岩和大坊成矿花岗闪长斑岩进行了LA-MC-ICP-MS锆石U-Pb测年,结果表明宝山花岗闪长斑岩、花岗闪长质隐爆角砾岩和大坊花岗闪长斑岩的侵位年龄分别为156. 3±0. 9Ma、157. 1±1. 8Ma和154. 5±1. 0Ma,三者在误差范围内一致,均为晚侏罗世岩浆活动的产物;锆石Hf同位素研究表明,宝山和大坊矿床的成矿岩体均主要为古元古代地壳物质部分熔融的产物,并有幔源组分的加入;锆石微量元素分析结果显示,上述三类岩石的锆石具有相似的稀土元素配分模式,显示它们可能是同一期岩浆作用的产物。宝山矿区花岗闪长斑岩中锆石的Ce~(4+)/Ce~(3+)比值平均为355,与全球典型的含铜斑岩的Ce~(4+)/Ce~(3+)比值( 300)相似。而大坊矿区花岗闪长斑岩中锆石的δEu平均为0. 48,与宝山岩体δEu平均值(0. 42)相近,指示二者具有相对较高的氧逸度,均为与铜金多金属矿化有关的斑岩体。锆石U-Pb年龄、Hf同位素及微量元素特征表明,大坊金矿和宝山铜多金属矿床均与矿区花岗闪长斑岩具有时空及成因联系,共同构成钦杭成矿带中段一套与花岗闪长斑岩有关的Cu(Mo)-Pb-Zn-Au-Ag成矿系统。