Hydrological and geochemical controls governing the distribution of trace metals in a mine-impacted lake

Factors controlling the distribution of mining-derived Cu, Pb and Zn in the waters and bottom sediments of a large Andean lake (Lago Junin, Peru) have been assessed based on sample collections in May/June 1997 (dry season) and February/March 1998 (wet season). Relatively low levels of trace metals detected in surface waters of the lake during the dry season contrasted greatly with the high values observed during the wet period. Dry season concentrations of total Zn, Cu and Pb in the central lake basin averaged 41, 4.4 and 0.24 µg/L, respectively. In contrast, the respective wet season concentrations of total Zn, Cu and Pb in areas of the main basin ranged up to 387, 52 and 40 µg/L. The seasonal variability in metal concentrations largely reflects an increase in the concentration of particulate metal phases during the wet season. Such observations can be attributed to changes in sediment loadings associated with mining-derived river inputs and changes in lake circulation resulting from hydroelectric dam operations. Surface sediments are characterized by lake-wide enrichments of Zn, Cu and Pb, with maximum concentrations reaching as high as 5, 0.25 and 0.7 wt%, respectively. Estimated rates of authigenic metal accumulation are not sufficient to account for the elevated metal concentrations in the main basin of the lake, indicating that metal distributions are governed by the accumulation of metal-rich particulates. Variations in the spatial distributions of Zn, Cu and Pb are suggested to be a function of varying host phases and textural sorting.     

Lead isotopic systematics of major river sediments: a new estimate of the Pb isotopic composition of the Upper Continental Crust

The lead isotopic composition of river sediments is reported in the present work for the Earth's major river basins, from old cratonic to young orogenic areas and from subarctic to tropical climates. Sediment samples from these large river basins provide a useful tool to calculate the average upper crustal composition because they are large-scale integrated samples of the weathering products of the present-day Upper Continental Crust (UCC). Two different and complementary calculations were done to estimate the average lead isotopic composition of the UCC. The first, based on the flux weighted average of particulate lead delivered by the rivers, gave values of 19.07, 15.74 and 39.35 for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios, respectively. To avoid over-estimating the contribution of orogenic areas, which produces a bias (because the flux of particulate lead depends strongly on the physical erosion rate), a second calculation was done by averaging with drainage areas of each river basin. This gave values of 18.93, 15.71 and 39.03 for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios, respectively. These direct calculations of the lead isotopic composition of the UCC are similar and are in agreement with previous estimates made using an indirect approach.     

云南禄劝噜鲁铅锌矿床铷-锶同位素年代学与硫、铅同位素地球化学特征

云南禄劝噜鲁铅锌矿床地处扬子地块西南缘,矿体赋存于下寒武统梅树村组下段,呈脉状、似层状产出。矿石矿物主要有方铅矿、闪锌矿、黄铁矿等;脉石矿物主要有重晶石、石英、方解石。噜鲁铅锌矿床硫化物成矿时的~(87)Sr/~(86)Sr值为0.7112~0.7115,暗示成矿物质可能来自于基底地层;Rb-Sr等时线年龄为202.8±1.4Ma,成矿年龄为印支晚期—燕山早期。硫化物硫同位素组成δ~(34)S变化范围为6.33‰~9.75‰,暗示成矿流体中的硫主要是海相硫酸盐热化学还原的产物;铅同位素~(206)Pb/~(204)Pb、~(207)Pb/~(204)Pb、~(208)Pb/~(204)Pb变化范围分别为18.259~18.342、15.608~15.639、38.46~38.821,位于上地壳和造山带铅演化线之间,落入基底岩石(昆阳群)及不同时代碳酸盐岩铅同位素组成范围内,表明成矿物质具有壳源特征,主要由基底岩石提供。综合各类地质-地球化学信息认为,噜鲁铅锌矿床成矿流体中不同组分来源不同,但主要来自于基底地层,成矿机制是在印支运动强驱动力的作用下,促使含矿基底地层成矿元素活化-迁移混合-空间就位,形成工业矿床。     

Nd,Sr and Pb isotopic and REE geochemical study of some Miocene submarine hydrothermal deposits (Kuroko deposits) in Japan

Neodymium, Sr and Pb isotopic compositions, along with rare earth element (REE) concentrations were determined for twelve black ores and one yellow ore from twelve localities of the Kuroko deposits, Japan. The ores were generated by submarine hydrothermal activity during the Miocene age. Neodymium isotopic compositions of the ores (_Nd: –4.9 to +6.5) mostly overlap with spatially associated igneous rocks. On a Nd versus Sr isotopic correlation diagram, however, ⁸⁷Sr/⁸⁶Sr ratios are shifted from the associated igneous rocks towards the higher contemporaneous seawater ratio. REE patterns are highly variable, ranging from light REE enriched to depleted, and show no Ce anomalies, as would be expected if they were derived from seawater. These results suggest that the REEs contained in ores were mainly derived from the associated igneous rocks, but that the ore Sr is a mixture derived from both seawater and the igneous rocks. Most Pb isotopic compositions fall within the range defined by the associated igneous rocks (²⁰⁶Pb/²⁰⁴Pb=18.35–18.84, ²⁰⁷Pb/²⁰⁴Pb=15.59–15.97 and ²⁰⁸Pb/²⁰⁴Pb=38.53–39.90), although several samples have very radiogenic compositions that were most likely derived from basement rocks. Our new Pb isotopic results display greater variation, and have a larger range of more radiogenic compositions than has been noted previously for these ores. In addition, the black ore with the most radiogenic Pb isotopic composition also has the least radiogenic Nd isotopic composition. This suggests that at least some of the Pb contained in the ores was derived mainly from older basement rocks. The large positive Eu anomalies for some black ores are consistent with a high-temperature origin for the parental fluids, irrespective of the source rock. The single yellow ore examined, however, has a small negative Eu anomaly, which may indicate derivation from a lower temperature fluid. Previous studies suggested that the Kuroko ores were formed in the presence of organic materials in an anoxic basin. Combined Nd, Sr, Pb and Os isotopic and REE abundance data indicate that multiple sources were involved in the genesis of Kuroko ores.     

The Hemlo gold deposit,Ontario: A geochemical and isotopic study

The Hemlo deposit, near Marathon, Ontario, is one of the largest gold deposits in North America. It is stratiform within Archean metamorphosed volcano-sedimentary rocks. The main ore zone is composed of pyritic, sericitic schist, and massive barite. This is the first report of stratiform barite in the Archean of North America, but other occurrences have since been found west of Hemlo. The mineralization is substantially enriched in Au, Mo, Sb, Hg, Tl and V and lacks carbonate. Because of metamorphism and deformation of the body its genesis is uncertain.${}^{87}\text{Sr}{}^{86}\text{Sr}$ of .7017 for barite from the deposit is similar to that of the sedimentary barite west of Hemlo and to initial ratios of contemporaneous volcanic rocks. At the base of the main ore zone, barite with δ^34S of +8 to +12%. was deposited with ~0%. pyrite. Upward, both barite and pyrite get isotopically lighter, with minimum values for pyrite, to ?17.5%, in non-baritic schist forming the upper part of the ore zone. In drill section, Au grades correlate with the isotopic composition of pyrite. This, and the association of fractionated sulphide with sulphate, suggests that Au, pyrite and barite were deposited contemporaneously. The linked, asymmetric distributions of S minerals and isotopic distributions, which are continuous from section to section, and the isotopic similarity of the Hemlo and western barites are consistent with a syngenetic depositional model.Two sources for the S minerals are considered. In the first, exogenous sulphate from a restricted basin were partially reduced in a geothermal system to form ³⁴S-depleted sulphide. In the second, the sulphate and sulphide are of magmatic-hydrothermal origin. Sulphate and fractionated sulphide are uncommon in Archean rocks, but one or both occur with unusual frequency in major Archean gold deposits. Hydrothermal fluids of moderately high , containing sulphate and permitting isotopic fractionation between oxidized and reduced S species, may have favoured the dissolution, transport and precipitation of Au.     

The north-eastern Polish anorthosite massifs: petrological, geochemical and isotopic evidence for a crustal derivation

ABSTRACT Deeply buried 1.5 Ga Polish anorthosites, accessible only by bore holes, reveal diagnostic features of some massif-type anorthosites (polybarism, jotunitic parent magma), diapirically emplaced in the mid crust together with the rapakivi granites of the EW-trending Mazury complex, intruded along a major crustal discontinuity. Geochemical modelling and isotope data corroborate recent experimental work on the basaltic system in dry conditions: the source rock of the parental magma is a gabbronorite, necessarily lying in the lower crust. Since no Archaean crust is known in the region, high initial ¹⁸⁸Os/¹⁸⁷Os ratios for sulphide-oxide isochrons and negative ε_Nd values are best accounted for by melting a ∼ 2.0 Ga mafic crust.     

Occurrence of fossil organic matter in modern environments: Optical, geochemical and isotopic evidence

This study relates to the input and fate of fossil organic matter (FOM) in the modern environment, and focuses on two experimental watersheds overlying Jurassic marls: Le Laval and Le Brusquet (1 km² in area), located near Digne, Alpes-de-Haute-Provence, France. Considering that FOM delivery is mainly a result of different processes affecting sedimentary rocks [(bio)chemical and mechanical weathering], samples from different pools were collected: bedrocks, weathering profiles, soils and riverine particles. The samples were examined using complementary techniques: optical (palynofacies methods), geochemical (Rock-Eval 6 pyrolysis, C/N ratio), molecular (gas chromatography/mass spectrometry) and isotopic (stable C isotopic composition). As a result, FOM markers were identified and tracked through the different pools. The results highlight the contribution of FOM, which can be found in all the studied pools. Transfer of FOM between bedrocks/weathering profiles (governed mainly by chemical weathering) and bedrocks/riverine particles (governed mainly by mechanical weathering) reveals any qualitative change. Weathering profiles/soils transition [governed by (bio)chemical weathering] is characterized by alteration of the FOM, which is difficult to describe because fossil material is mixed with recent organic matter (ROM). Despite this latter point, the study provides evidence for a relative resistance of FOM to weathering processes and points to its contribution to the modern geosystem and the C cycle.     

新疆博格达白杨沟的枕状熔岩：岩石地球化学和Sr-Nd-Pb同位素特征

新疆博格达造山带北段东侧白杨沟地区分布有大面积的晚石炭世至早二叠世的火山岩,岩石主要由亚碱性玄武岩和安山岩组成,其中分布有大量保存极好的枕状熔岩。枕状熔岩主要为基性熔岩,SiO2含量50.17%～54.66%,Al2O3为13.10%～16.44%,MgO为4.62%～7.89%,TiO2为1.23%～2.79%,CaO为7.06%～13.07%,Na2O为2.76%～4.99%,K2O为0.07%～0.82%。基性熔岩的大离子亲石元素(LILE)一组为富集如Rb和Ba,另一组相对亏损;高场强元素(HFSE)如Nb和Ta在N-MORB标准化图解上都具有明显的负异常。熔岩的稀土元素在球粒陨石标准化配分图解中表现为总体平坦,轻稀土元素(LREE)轻微富集的右倾曲线,δEu为0.89～1.12。从Sr-Nd-Pb同位素组成来看,εNd(t)为+2.8～+3.1,143Nd/144Nd(i)为0.512407～0.512422,εSr(t)为-14.0～-17.5、87Sr/86Sr(i)为0.70293～0.70317、206Pb/204Pb(i)为17.622～17.835、207Pb/204Pb(i)为15.3...     

Pb isotopic composition,colour, and microstructure of monazites from a polymetamorphic rock in Antarctica

A moderate- to high-grade regionally metamorphosed paragneiss from Antarctica contains monazites of several different colours — brown, yellow and grey. Each colour type has a distinctive U-Pb isotopic composition which appears to result from different proportions of radiogenic Pb loss. Isotopic differences are neither related to La, Nd, Ce, P, Ca, Ti (and/or Ba), nor to U or Th content. All colour types have similar structures at the submicron scale, as determined by both conventional and high-resolution transmission electron microscopy (TEM). These show that the grains are essenttially non-metamict but are composed of 100 Å crystalline domains misoriented from each other by no more than 2× 10^–3 radians, and separated by narrow confused boundary regions where misorientation is probably accommodated by imperfect atomic arrangements. These regions of mismatch form potential zones of high permeability/diffusivity which are believed to be fundamental to the isotopic and colour differences between grains. Colour type is apparently related to the capacity of different minerals to shield included monazite grains from fluids circulating in the rock system.The well aligned monazite U — Pb analyses produce concordia intercepts of 2429 _–16 ⁺¹⁷ Ma and 1087±29 Ma. Both ages are comparable to those of major geological events in this part of Antarctica. They are interpreted in terms of isotopic resetting through Pb loss, and original monazite crystallisation is thought to have occurred somewhat earlier, possibly at the time this terrain first underwent granulite-facies metamorphism, about 3070 Ma ago.     

Transition from calc-alkaline to potassium-rich magmatism in subduction environments: geochemical and Sr, Nd, Pb isotopic constraints from the island of Vulcano (Aeolian arc)

The problem of mantle metasomatism vs. crustal contamination in the genesis of arc magmas with different potassium contents has been investigated using new trace element and Sr–Nd–Pb isotopic data on the island of Vulcano, Aeolian arc. The analysed rocks range in age from 120 ka to the present day, and cover a compositional range from basalt to rhyolite of the high-K calc-alkaline (HKCA) to shoshonitic (SHO) and potassic (KS) series. Older Vulcano products (>30 ka) consist of HKCA–SHO rocks with SiO₂=48–56%. They show lower contents of K₂O, Rb and of several other incompatible trace element abundances and ratios than younger rocks with comparable degree of evolution. ⁸⁷Sr/⁸⁶Sr ranges from 0.70417 to 0.70504 and increases with decreasing MgO and compatible element contents. ²⁰⁶Pb/²⁰⁴Pb ratios display significant variations (19.31 to 19.76) and are positively correlated with MgO, ¹⁴³Nd/¹⁴⁴Nd (0.512532–0.512768), ²⁰⁷Pb/²⁰⁴Pb (15.66–15.71) and ²⁰⁸Pb/²⁰⁴Pb (39.21–39.49). Overall, geochemical and isotopic data suggest that the evolution of the older series was dominated by assimilation–fractional crystallisation (AFC) with an important role for continuous mixing with mafic liquids. Magmas erupted within the last 30 ka consist mostly of SHO and KS intermediate and acid rocks, with minor mafic products. Except for a few acid rocks, they display moderate isotopic variations (e.g. ⁸⁷Sr/⁸⁶Sr=0.70457–0.70484; ²⁰⁶Pb/²⁰⁴Pb=19.28–19.55, but ²⁰⁷Pb/²⁰⁴Pb=15.66–15.82), which suggest an evolution by fractional crystallisation, or in some cases by mixing, with little interaction with crustal material. The higher Sr isotopic ratios (⁸⁷Sr/⁸⁶Sr=0.70494–0.70587) of a few, low-volume, intermediate to acid rocks support differentiation by AFC at shallow depths for some magma batches. New radiogenic isotope data on the Aeolian islands of Alicudi and Stromboli, as well as new data for lamproites from central Italy, are also reported in order to discuss along-arc compositional variations and to evaluate the role of mantle metasomatism. Geochemical and petrological data demonstrate that the younger K-rich mafic magmas from Vulcano cannot be related to the older HKCA and SHO ones by intra-crustal evolutionary processes and point to a derivation from different mantle sources. The data from Alicudi and Stromboli suggest that, even though interaction between magma and wall rocks of the Calabrian basement during shallow level magma evolution was an important process locally, a similar interpretation can be extended to the entire Aeolian arc. Received: 27 September 1999 / Accepted: 24 May 2000     

Use of Sr isotopes as a tool to decipher the soil weathering processes in a tropical river catchment,southwestern India

River water composition (major ion and ⁸⁷Sr/⁸⁶Sr ratio) was monitored on a monthly basis over a period of three years from a mountainous river (Nethravati River) of southwestern India. The total dissolved solid (TDS) concentration is relatively low (46 mg L⁻¹) with silica being the dominant contributor. The basin is characterised by lower dissolved Sr concentration (avg. 150 nmol L⁻¹), with radiogenic ⁸⁷Sr/⁸⁶Sr isotopic ratios (avg. 0.72041 at outlet). The composition of Sr and ⁸⁷Sr/⁸⁶Sr and their correlation with silicate derived cations in the river basin reveal that their dominant source is from the radiogenic silicate rock minerals. Their composition in the stream is controlled by a combination of physical and chemical weathering occurring in the basin. The molar ratio of SiO₂/Ca and ⁸⁷Sr/⁸⁶Sr isotopic ratio show strong seasonal variation in the river water, i.e., low SiO₂/Ca ratio with radiogenic isotopes during non-monsoon and higher SiO₂/Ca with less radiogenic isotopes during monsoon season. Whereas, the seasonal variation of Rb/Sr ratio in the stream water is not significant suggesting that change in the mineral phase being involved in the weathering reaction could be unlikely for the observed molar SiO₂/Ca and ⁸⁷Sr/⁸⁶Sr isotope variation in river water. Therefore, the shift in the stream water chemical composition could be attributed to contribution of ground water which is in contact with the bedrock (weathering front) during non-monsoon and weathering of secondary soil minerals in the regolith layer during monsoon. The secondary soil mineral weathering leads to limited silicate cation and enhanced silica fluxes in the Nethravati river basin.     

U–Pb zircon ages, geochemical and isotopic compositions of granitoids in Songpan-Garze fold belt, eastern Tibetan Plateau: constraints on petrogenesis and tectonic evolution of the basement

The Songpan-Garze fold belt, located in the eastern part of the Tibetan Plateau, covers a huge triangular area bounded by the Yangtze (South China), the North China and the Tibetan Plateau blocks. In the northeastern part of the Songpan-Garze fold belt, the Yanggon and Maoergai granitoids provide insights into regional tectono-magmatic events, basement nature and tectonic evolution. U–Pb zircon SHRIMP dating shows that the Yanggon and Maoergai granitoids have magmatic crystallization ages of 221 ± 3.8 Ma and 216 ± 5.7 Ma, respectively. Both the granitoids display adakitic geochemical signatures, suggesting that their magma was derived from partial melting of thickened lower crust. Pb–Sr–Nd isotopic compositions for granitoids reveal that there is an unexposed Proterozoic basement in the Songpan-Garze belt, which has an affinity with the Yangtze block. During development of the Paleo-Tethys ocean, the basement of the Songpan-Garze belt would be a peninsula approaching the Paleo-Tethys ocean from the Yangtze block.     

Fluid inclusion and stable isotope study of the Cobre–Babilonia polymetallic epithermal vein system, Taxco district, Guerrero, Mexico

The Cobre–Babilonia vein system formed during a single major hydrothermal stage and is part of the Taxco district in Guerrero, southern Mexico. Homogenization and ice melting temperatures range from 160 to 290 °C and from − 11.6 to − 0.5 °C, respectively. We determined an approximate thermal gradient of 17 to 20 °C per 100 m using fluid inclusions. A thermal peak marked by the 290 °C isotherm is interpreted as a major feeder channel to the veins. The highest content of Zn + Pb in ore coincides with the 220 and 240 °C isotherms. Salinities of mineralizing fluids range from 0.8 to 15.6 wt.% NaCl equiv, and are distributed in two populations that can be related with barren or ore-bearing vein sections, with 0.8 to 6 wt.% NaCl equiv and 7 to 15.6 wt.% NaCl equiv, respectively. δ¹³C and δ¹⁸O water values from calcite from the Cobre–Babilonia vein system and the Esperanza Vieja and Guadalupe mantos range − 5.4‰ to − 10.4‰ and 9.9‰ to 13.4‰, respectively. δ³⁴S values range from 0‰ to 3.2‰ and − 0.7‰ to − 4.3‰ in sphalerite, − 4‰ to 0.9‰ in pyrite, and − 1.4‰ to − 5.5‰ in galena. Both fluid inclusion and stable isotope data are compatible with magmatic and meteoric sources for mineralizing fluids. Also, sulfur isotope compositions suggest both magmatic and sedimentary sources for sulfur.     

新疆磁海铁矿床Fe-O-S同位素和元素地球化学示踪

新疆磁海铁矿位于北山构造-成矿带西端,以磁海矿段为主要组成部分,铁矿体主要为透镜状、似层状,围岩以辉绿岩为主,二者接触线截然且平直;另外一种矿体产在基性岩体与地层接触带的石榴子石透辉石矽卡岩岩体内,整个矽卡岩岩体即为铁矿体。通过野外矿床特征与矿相学研究,成矿过程可分为:(1)矿浆期,以磁铁矿+单斜辉石+普通角闪石的近同时产出为特征;(2)矽卡岩期,先期以石榴子石+透辉石+磁铁矿为特征,后期以透闪石/阳起石+石英+磁黄铁矿+黄铜矿+黄铁矿的组合为特征。通过对矿浆期及矽卡岩期典型矿物的地球化学及Fe、S、O同位素结果分析,认为矿浆期铁质具有幔源特征,矽卡岩期成矿流体对矿浆期具有继承性。通过与前人研究结果对比分析,认为磁海成矿可能形成于塔里木地区二叠纪地幔柱背景,含矿母岩浆可能为地幔柱的分支。     

Tectonics of the Siberian Craton: Interpretation of geological, geophysical, geochronological, and isotopic geochemical data

The tectonic scheme of the Siberian Craton proposed in this paper is compiled on the basis of a geological map of the craton prepared from numerous magnetometric maps and gravity measurements on various scales, the scheme of axes of magnetic anomalies, and the synthesis of geological information on the exposed territories. The shields and platform territories of the ancient Siberian Craton comprises Archean blocks and Paleoproterozoic foldbelts. The granite-greenstone terranes and granulite-gneiss domains were formed in the Meso- and Neoarchean. The granite-greenstone terranes exposed and overlapped by sedimentary cover are identical, although they generally differ in internal structure and rock compositions both at the infra- and supracrustal levels. The Archean granulite-gneiss domains are recognized either as special tectonic units or as deep sections of granite-greenstone terranes. Two groups of the Paleoproterozoic collisional belts that amalgamated separate Archean blocks of the Siberian Craton into a common stable structural unit evolved 2.1–1.9 and 1.9–1.8 Ga ago. Three types of deep faults arose in the Paleoproterozoic: (1) translithospheric fault zones as boundaries of tectonic blocks and collisional belts, (2) intracrustal fault zones that originated as a result of nonuniform uplift of particular segments of the common plate, and (3) transcrustal zones formed in a plate that overrode another, plunging plate.     

Pb, Sr, and Nd isotopic and chemical evidence for a primitive island arc emplacement of the El Arco porphyry copper deposit (Baja California, Mexico)

The El Arco porphyry copper deposit is located in central Baja California and is a resource containing >600 Mt of ore with ∼0.6% copper. It was emplaced within a relatively primitive Jurassic island arc and it was subsequently metamorphosed and intruded by the Cretaceous Peninsular Ranges batholith. The porphyritic stock intrusion and ore formation at El Arco has recently been dated at ∼165 Ma [Valencia et al. GEOS 24:189 (2004)]. This age is much older than Aptian-Albian K–Ar ages previously reported from El Arco [Barthelmy, Geology of El Arco-Calmallí area, Baja California, México. MSc Thesis, San Diego State University, CA (1975); Baja California Geology. San Diego State University, CA, pp 127–138 (1979)]. The copper mineralization at El Arco is concentrated in a core of potassic alteration in a dioritic porphyritic stock surrounded by propylitic alteration in andesitic lavas. Mafic dikes that intruded the deposit are not mineralized, but they are affected by post-ore low-grade metamorphism. The dikes are compositionally the most primitive rocks, while host rock andesites and the porphyry stock display typical volcanic arc characteristics. The Pb isotope data from sulfides, feldspars, quartz, and whole-rock samples indicate that: (1) the copper-bearing porphyry stock and the surrounding andesites evolved from a similar source with an average μ-value of 9.43; (2) no external Pb was added during mineralization; (3) some Pb isotope compositions were slightly disturbed by a later metamorphic event. Strontium and Nd isotopes show that the magmas evolved from a depleted mantle reservoir with no involvement of older continental crust. Our data favor a model for the formation of the El Arco deposit linked to a Triassic to Jurassic intra-oceanic arc system, cropping out at the western margin of central Baja California in the Cedros-Vizcaíno region. The intra-oceanic arc together with the El Arco deposit was accreted to the active continental margin of North America and metamorphosed during the Early Cretaceous. This model is in disagreement to earlier models that favor the El Arco deposit formation being linked to the Cretaceous continental margin.     

Chemical and isotopic (Pb,Sr) zonation in a peraluminous granite pluton: role of fluid fractionation

The Davis Lake pluton (DLP, ~800 km²) of southwestern Nova Scotia, Canada, part of the large peraluminous South Mountain batholith of ca. 380 Ma (U/Pb zircon, Ar/Ar mica), consists of granite and subordinate topaz–muscovite leucogranite that hosts greisen tin-base metal mineralization. A new Pb–Pb isochron age for leucogranite from the most evolved part of the DLP indicates a crystallization age of 378±3.6 Ma, coincident with other radiometric ages of the DLP (Rb–Sr, Re–Os, Pb–Pb). The intrusion displays a compositional zonation defined by lead and strontium isotopic ratios, as well as some major elements (e.g., Si, F), incompatible trace elements (e.g., Li, Rb, Ta, U, Sn), and elemental ratios (e.g., K/Rb and Nb/Ta). The greisens and the leucogranites that host them are characterized by extreme radiogenic compositions for Pb and Sr, and their chemical-isotopic trends are extensions of the trends displayed by the less evolved granites. The covariations of the isotopic ratios with several major and trace elements and elemental ratios as well as the Pb–Pb and Rb–Sr isochrones indicate that all phases of the intrusion originated from a homogeneous parental magma. The granitoid magma underwent extensive fractional crystallization of feldspars, minor biotite and accessory minerals (monazite, apatite and zircon) in a compositionally zoned magma chamber that was subsequently accompanied by fluid fractionation, during which time the internally derived fluorine-rich fluids modified the Rb/Sr, U/Pb and Th/Pb ratios, leading to distinct variations of ⁸⁷Sr/⁸⁶Sr, ²⁰⁶Pb/²⁰⁴Pb, ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb isotopic ratios. These data therefore document the evolution of a granitic magma through magmatic (i.e., crystal fractionation), orthomagmatic (i.e., crystal-fluid fractionation) and hydrothermal (i.e., fluid fractionation) stages that culminated in the formation of a tin-base metal deposit. The Pb isotope data also constrain the source region for the DLP as being Avalonian basement that, by inference, must underlie much of the Meguma Terrane.Editorial responsibility: T.L. Grove     

Nd-Sr isotopic and geochemical systematics in Cambrian boninites and tholeiites from Victoria,Australia

Rocks with boninitic affinities have been recognised in a number of ophiolites, including the Cambrian Heathcote and Mt Wellington Greenstone Belts of Victoria. Boninites and high-Mg andesites from the Heathcote Greenstone Belt show a restricted range of initial _Nd values of between +3.3 to +5.8. Extremely refractory boninites from the Mt Wellington Greenstone Belt have _Nd ranging from +1.3 to –9. Ti/Zr is positively correlated with Sm/Nd with the Heathcote lavas generally possessing greater depletion of Ti and enrichment of Zr relative to the middle and heavy REE with increasing LREE/HREE. These data are consistent with the generation of boninites by partial melting of refractory peridotite following invasion by LREE- and Zr-enriched, low _Nd fluids. Tholeiites overlying the boninites in both greenstone belts have flat REE patterns and _Nd+5, lower than that anticipated for lavas derived from depleted MORB source reservoirs in the Cambrian, suggesting that their source was also contaminated by a LREE-enriched, low _Nd component similar to that involved in the generation of the Howqua boninites. The added components have characteristics compatible with their derivation from subducted altered oceanic crust and/or from wet subducted sediments. The identification of boninites and other low-Ti lavas in the Victorian greenstone belts is strong evidence for island arc development in southeastern Australia during the Lower Cambrian and provides further support for a subduction-related origin for many ophiolites.