Early Albian marine environments in Madagascar: An integrated approach based on oxygen,carbon and strontium isotopic data

New palaeotemperature reconstructions have been obtained on the basis of oxygen isotopic analysis of 178 aragonitic shell samples taken from specimens of three ammonoid orders (and some corresponding families): Phylloceratida (Phylloceratidae), Lytoceratida (Tetragonitidae) and Ammonitida (Oppeliidae, Desmoceratidae, Silesitidae, Cleoniceratidae and Douvilleiceratidae). Those obtained from aragonite shells, secreted in the lower epipelagic and in the middle mesopelagic zones during coolest season (winter), range from 15.4 to 16.8 °C, and from 11.8 to 12.0 °C, respectively. Presumed spring/autumn palaeotemperatures obtained from aragonite shells, secreted apparently in the upper and lower epipelagic, upper and middle mesopelagic zones, are somewhat higher. Presumed summer palaeotemperatures, calculated apparently for the upper and lower epipelagic, and upper mesopelagic zones range from 19.4 to 21.7 °C, from 17.7 to 19.4 °C, and from 14.4 to 16.1 °C, respectively. The predominant part of investigated ammonoids from Madagascar inhabited the epipelagic zone, but some phylloceratid, tetragonitid and silesitid ammonoids preferred deeper, cooler conditions (upper-middle mesopelagic zone). The study supports the hypothesis that Madagascar was located in middle latitudes within the tropical-subtropical climatic zone during the early Albian. Available carbon and strontium isotope data allow us to assume a more or less expressed carbon and strontium isotope stratification of the water column in this region in the early Albian. On the basis of the stable isotope data, following partly Lukeneder (2015), two large ethological groups can be recognised mainly in mid-aged and adult ammonoids. Some ammonoids (group 1) preferred apparently mesopelagic conditions, and to a lesser degree the epipelagic zone, being mainly cool-requiring animals. However, a significant part of the isotopically investigated ammonoids (group 2) preferred, on the contrary, only epipelagic conditions, being mainly thermophilic dwellers.     

Petrogenesis and geodynamic evolution of the Kajan Neogene subvolcanic rocks,Nain, Central Iran

Kajan subvolcanic rocks in the Urumieh–Dokhtar magmatic arc (UDMA), Central Iran, form a Late Miocene-Pliocene shallow-level intrusion. These subvolcanics correspond to a variety of intermediate and felsic rocks, comprising quartz diorite, quartz monzodiorite, tonalite and granite. These lithologies are medium-K calc-alkaline, with SiO₂ (wt.%) varying from 52% (wt.%) to 75 (wt.%). The major element chemical data also show that MgO, CaO, TiO₂, P₂O₅, MnO, Al₂O₃ and Fe₂O₃ define linear trends with negative slopes against SiO₂, whilst Na₂O and K₂O are positively correlated with silica. Contents of incompatible trace elements (e.g. Ba, Rb, Nb, La and Zr) become higher with increasing SiO₂, whereas Sr shows an opposite behaviour. Chondrite-normalized multi-element patterns show enrichment in LILE relative to HFSE and troughs in Nb, P and Ti. These observations are typical of subduction related magmas that formed in an active continental margin. The Kajan rocks show a strong affinity with calc-alkaline arc magmas, confirmed by REE fractionation (La_N/Yb_N = 4.5–6.4) with moderate HREE fractionation (Sm_N/Yb_N = 1.08–1.57). The negative Eu anomaly (Eu/Eu* <1), the low to moderate Sr content (< 400 ppm) and the Dy/Yb values reflect plagioclase and hornblende (+- clinopyroxene) fractionation from a calc-alkaline melt Whole–rock Sr and Nd isotope analyses show that the ⁸⁷Sr/⁸⁶Sr initial ratios vary from 0.704432 to 0.705989, and the ¹⁴³Nd/¹⁴⁴Nd initial ratios go from 0.512722 to 0.512813. All the studied samples have similar Sr-Nd isotopes, indicating an origin from a similar source, with granite samples that has more radiogenic Sr and low radiogenic Nd isotopes, suggesting a minor interaction with upper crust during magma ascent. The Kajan subvolcanic rocks plot within the depleted mantle quadrant of the conventional Sr-Nd isotope diagram, a compositional region corresponding to mantle-derived igneous rocks.     

Water-rock-tailings interactions and sources of sulfur and metals in the subtropical mining region of Taxco,Guerrero (southern Mexico): A multi-isotopic approach

Multi-isotope (H, O, S, Sr, Pb) systems coupled with conventional (major and trace element) hydrogeochemical analysis were applied to determine the origin of water, to model water-rock-tailings interactions and for source apportionment of sulfur and associated toxic metals in the mining region of Taxco, Guerrero in southern Mexico. Oxygen and H isotopes indicate that meteoric water in the zone is rainwater undergoing varying degrees of isotopic fractionation by atmospheric evaporation whereas Sr isotopes trace the interaction of pristine water from volcanics of the regional recharge zone and subsequently flowing through sandstone and shale to spring points. Leachates form from two distinctive sources (spring water and surface water) having differential interactions with bedrocks prior to entering the tailings. Compared to pristine water, leachates are enriched in sulfate, metals (e.g. Fe, Mn, Pb and Zn) and metalloids (e.g. As). The sulfur isotopic composition of ore-sulfides, leachates, secondary precipitates, regional surface water and hypogenic sulfates is described in terms of a two-component mixing model with shale of Mexcala and limestone of Morelos formations representing the light and heavy end-members, respectively, whereas Sr isotopic composition is bracketed combining three lithogenic (Mexcala/Morelos, Tilzapotla and Taxco Schist) sources. Finally, leachates have a mixture of lead from ore-sulfides and Taxco Schist Formation (Family I) or from ore-sulfides alone (Family II). The application of multiple environmental isotopic techniques is an outstanding tool for elucidating complex interactions of water with bedrocks and tailings and for determining the source of sulfur and toxic metal from mining and other metal polluted environments.     

Geochemistry of Paraná-Etendeka basalts from Misiones,Argentina: Some new insights into the petrogenesis of high-Ti continental flood basalts

The Early Cretaceous (∼135–131 Ma) Paraná-Etendeka continental flood basalts, preserved in bulk in the Paraná basin of southern Brazil and vicinity, have been divided into low-Ti and high-Ti types that govern the southern and northern halves of the basin, respectively. We have examined a new sample set from the southern margin of the northern high-Ti segment of Paraná basalts in Misiones, northeastern Argentina. These basalts are strongly to moderately enriched in TiO₂ (2–4 wt.%), have relatively high Ti/Y (300–500), low MgO (3.5–6.5 wt.%), and high Fe (FeO(tot) 12–14 wt.%) and belong to the Pitanga and Paranapanema magma types of Peate et al. (1992). Nd and Sr isotope compositions are quite unvarying with ε_Nd (at 133 Ma) values of −4.6 to −3.6 and initial ⁸⁷Sr/⁸⁶Sr of 0.7054–0.7059 and show no variation with fractionation. Compared to high-Ti lavas in the central and northern parts of the Paraná high-Ti basalt segment, the lavas from Misiones are similar to those in the northeastern magin of the basin but less radiogenic in initial Nd isotope composition than those in the central part. This variation probably reflects mixed EM1-EM2 source components in the sublithospheric mantle. A polybaric melt model of a sublithospheric mantle source at the garnet lherzolite-spinel lherzolite transition is compatible with the observed Ti budget of the Pitanga and Paranapanema lavas, regardless of the Nd isotope composition of their purported source.     

High Precision Sr‐Nd‐Hf‐Pb Isotopic Compositions of USGS Reference Material BCR‐2

The Lamont‐Doherty Earth Observatory radiogenic isotope group has been systematically measuring Sr‐Nd‐Pb‐Hf isotopes of USGS reference material BCR‐2 (Columbia River Basalt 2), as a chemical processing and instrumental quality control monitor for isotopic measurements. BCR‐2 is now a widely used geochemical inter‐laboratory reference material (RM), with its predecessor BCR‐1 no longer available. Recognising that precise and accurate data on RMs is important for ensuring analytical quality and for comparing data between different laboratories, we present a compilation of multiple digestions and analyses made on BCR‐2 during the first author's dissertation research. The best estimates of Sr, Nd and Hf isotope ratios and measurement reproducibilities, after filtering at the 2s level for outliers, were ⁸⁷Sr/⁸⁶Sr = 0.705000 ± 11 (2s, 16 ppm, n = 21, sixteen digestions, one outlier), ¹⁴³Nd/¹⁴⁴Nd = 0.512637 ± 13 (2s, 25 ppm, n = 27, thirteen digestions, one outlier) and ¹⁷⁶Hf/¹⁷⁷Hf = 0.282866 ± 11 (2s, 39 ppm, n = 25, thirteen digestions, no outliers). Mean Nd and Hf values were within error of those reported by Weis et al. (2006, 2007) in their studies of RMs; mean Sr values were just outside the 2s uncertainty range of both laboratories. Moreover, a survey of published Sr‐Nd‐Hf data shows that our results fall within the range of reported values, but with a smaller variability. Our Pb isotope results on acid leached BCR‐2 aliquots (n = 26, twelve digestions, two outliers) were ²⁰⁶Pb/²⁰⁴Pb = 18.8029 ± 10 (2s, 55 ppm), ²⁰⁷Pb/²⁰⁴Pb = 15.6239 ± 8 (2s, 52 ppm), ²⁰⁸Pb/²⁰⁴Pb = 38.8287 ± 25 (2s, 63 ppm). We confirm that unleached BCR‐2 powder is contaminated with Pb, and that sufficient leaching prior to digestion is required to achieve accurate values for the uncontaminated Pb isotopic compositions.     

Rb–Sr Dating of Gold‐Bearing Pyrite in the Jinchang Porphyry Cu–Au Deposit,Heilongjiang Province,NE China

The Jinchang Cu–Au deposit in Heilongjiang Province, NE China, is located in the easternmost part of the Central Asian Orogenic Belt. Rb–Sr analyses of auriferous pyrite from the deposit yielded an isochron age of 113.7 ±2.5 Ma, consistent with previously reported Re–Os ages. Both sets of ages represent the timing of Cu–Au mineralization because (i) the pyrite was separated from quartz–sulfide veins of the mineralization stage in granite porphyry; (ii) fluid inclusions have relatively high Rb, Sr, and Os content, allowing precise measurement; (iii) there are no other mineral inclusions or secondary fluids in pyrite to disturb the Rb–Sr or Re–Os decay systems; and (iv) the closure temperatures of the two decay systems are ≥500°C (compared with the homogenization temperatures of fluid inclusions of 230–510°C). It is proposed that ore‐forming components were derived from mantle–crust mixing, with ore‐forming fluids being mainly exsolved from magmas with minor amounts of meteoric water. The age of mineralization at Jinchang and in the adjacent regions, combined with the tectonic evolution of the northeast China epicontinental region, indicates that the formation of the Jinchang porphyry Cu–Au deposit was associated with Early Cretaceous subduction of the paleo‐Pacific Plate.     

Geodynamic setting,structure, and composition of continuous trachybasalt-trachyandesite-rhyolite series in the north of Altai-Sayan area: the role of crust-mantle interaction in continental magma formation

The geologic positions and geochemical and isotope parameters of the Ordovician-early Silurian and Early-Middle Devonian continuous volcanic series of the Minusa basin and its mountainous framing are compared. Both series are composed mostly of moderately alkaline rocks with variations in SiO₂ contents from 45 to 77 wt.%. The Ordovician-early Silurian series differs from the Early-Middle Devonian one in lower contents of TiO₂ (< 1.7 wt.%) and Fe₂O_3tot and higher contents of Al₂O₃ in all rock varieties and in the more fractionated REE patterns of trachybasalts. The compositions of both series reflect two simultaneous mechanisms of magma evolution. The main process was fractional crystallization leading to the formation of rocks from trachybasalts to trachyrhyodacites. The accessory mechanism was the contamination of fractionated melts by crustal material, anatectic melting of crust, and mixing of deep-seated magmas with crustal melts. These processes had specifics at each stage and were controlled by the composition of the sources of parental melts. Their geochemical and isotopic parameters (high alkalinity, high contents of lithophile elements, negative anomalies of Nb, Ta, and Ti, and enrichment in radiogenic Sr) point to the interaction of mantle plumes with the lithospheric mantle that was metasomatically transformed during the preceding Vendian-early Cambrian subduction processes.     

CCSD主孔榴辉岩中磷灰石的矿物化学特征及对榴辉岩中F、Cl、Sr等元素地球化学行为的影响

为探讨榴辉岩中磷灰石的矿物化学特征及榴辉岩中某些相关元素的地球化学行为,对中国大陆科学钻探(CCSD)主孔500~540m深度的榴辉岩样品进行了岩石化学及磷灰石的矿物化学分析。这些榴辉岩具有不同的矿物组成和化学成分,并可据此分为上下两段,上段500~530m为正常榴辉岩,下段530~540m为高Ti榴辉岩和高Ti-Fe榴辉岩,其原岩可能为类似于辉长质和苦橄质的基性—超基性岩石。其中的磷灰石成分没有明显差别,均为氟—磷灰石,其富F贫Cl的特征可能是造成榴辉岩中高盐度流体包裹体和全岩高F低Cl的主要原因。磷灰石普遍含有一定的Sr、S、Fe元素,多数还含有Cu、Pb、Zn等元素。榴辉岩中P2O5含量与其F、Cl、Sr、S元素的相关程度表明,磷灰石是榴辉岩中F元素的最主要储存库,也是Sr元素的重要储存库之一,而对于Cl元素则只是部分控制,与S元素则没有相关性。榴辉岩中F、Sr及Cl元素的地球化学行为主要受控于磷灰石,因此,在榴辉岩从进变质—退变质过程中,这些元素的活动性直接受控于磷灰石的稳定性。     

碳、氧、锶同位素在羌塘盆地龙尾错地区层序地层研究中的应用

结合野外露头层序地层研究,探讨了羌塘盆地龙尾错地区中上侏罗统地层层序地层划分及其C、O、Sr同位素响应.认为自中侏罗统布曲组(J2b)-上侏罗统雪山组一段(J3xs1)可划分出三个三级层序.其中布曲组-索瓦组二段下部,C、O、Sr同位素在同一层序内呈有规律变化:在TST体系域内δ13C、δ18O、87Sr/86Sr均值较高,在纵向变化曲线上表现为正偏,而在HST体系域内表现为相对的负偏.其纵向上的三次明显正偏与负偏可分别对应于三次海底的停滞与扩张.文章同时分析了个别异常样品的数据特征及其成因.