Strontium Isotopic Composition Research Articles

Oxygen-Carbon and Strontium Isotope Composition in Primary Carbonatites of the World: The Data Summary and Linear Trends

A statistical regression analysis was performed of a summary of borrowed literary isotopic data on 176 carbonatite occurrences worldwide (a total of 1829 paired δ18О-δ13С values in primary carbonatites). For most of the occurrences, distinct linear trends in δ18О-δ13С values were revealed, approximated in diagrams by vectors using the regression formula y = kx + b. Trends in three directions are distinguished. The dominating trend possesses the angular coefficient k in the range of 0.0÷+0.6, averaging at + 0.31 (direct correlation δ18О-δ13С). In the literature, it is associated with the Rayleigh high-temperature fractionation of carbonatite melts or with their sedimentary crustal contamination. The second trend with k from 0.0 to -0.7 (inverse correlation δ18О-δ13С) is associated with CO2 degassing from the melts. The third trend with k from +0.6 to +1.5 is rare. In other carbonatite occurrences, no linear trends in δ18О-δ13С values are detected. This may be a consequence of a combined action of the multidirectional linear trends. In this regard, the initial point of the trend vectors is accepted as a universal isotope indicator for all the carbonatite occurrences. In the δ18О-δ13С diagram, the box PC-90 is outlined in the field of the initial points, including 90 % of the primary carbonatite occurrences. The coordinates of the corner points of the box in δ18О-δ13С ‰ are (+5÷-8), (+5÷-5), (+5.5÷-2.5), (+12÷-2.5), (+12÷-7), (+9÷-8.5). The box PC-90 is subdivided into two parts by the carbon isotope composition, using the value δ13C = -5.2 ‰. This suggests that the deep sources differ in carbon isotope composition. No correlation is found in the oxygen-carbon and strontium isotope compositions in the carbonatites, which suggests that the deep sources are also heterogeneous in the strontium isotope composition.

Strontium Isotope Composition of Triassic Coastal and Shallow Marine Carbonates in the Western Balkanides, NW Bulgaria

Whole-rock samples of Triassic coastal and shallow marine carbonates were analyzed for their Sr isotope signatures and trace element concentrations were measured in order to assess the possible impact of diagenetic alteration. The 87Sr/86Sr ratios of Anisian to lower Carnian calcite micrites reproduce the global Triassic seawater variations fairly well. The recorded higher values can be explained by an influence from detrital aluminosilicate phases and a minor postdepositional alteration. The samples of tidal-flat dolomicrites from the base of the Anisian show no significant diagenetic overprint but have considerably more radiogenic 87Sr/86Sr signatures compared to the global Sr isotope curve that corresponds to the Triassic (Mesozoic) maximum. These anomalously high values may have resulted from some interaction between the dolomitizing brines and the underlying fluvial siliciclastics (Buntsandstein facies), but more likely from the high 87Sr/86Sr river waters discharged from a silicate-dominated drainage basin to the coastal area at the beginning of the Middle Triassic. This study demonstrates that bulk micrite can be used as a proxy for seawater 87Sr/86Sr after proper sample selection and diagenetic screening. It also suggests that the 87Sr/86Sr ratios of ancient carbonates precipitated in coastal settings should be interpreted with caution, considering the possible influence of continentally-derived fluids.

Application of major ions and Sr isotopes to indicate the evolution of river water and shallow groundwater chemistry in a typical endorheic watershed, northwestern China

Studying the hydrochemical evolution of river water and groundwater is vital for comprehending complex regional hydrological cycles and managing water resources. An investigation of hydrochemical evolution mechanism of river water and groundwater was executed in an arid and semi-arid endorheic watershed located in the eastern edge of Qaidam Basin, northwest China, by analyzing major ions and strontium isotopic compositions with the combination of hydrogeochemical methods, PMF model and Pearson correlation analysis. From upstream to downstream, the major ions, 87Sr/86Sr values and hydrochemical types of river water and groundwater show spatial variations. Major ions and 87Sr/86Sr analysis reveal that the hydrochmical compositions of river water and groundwater are primarily attributed to silicate weathering, carbonate weathering, evaporite weathering, and agricultural activity. The contribution of four factors affecting the hydrochemical evolution show obvious spatial variations along the flow path. The hydrochemical compositions of river water from the upstream to downstream are mainly contributed by carbonate and silicate weathering as well as weak evaporite weathering (<25%), which are affected by agricultural activity with a great contribution (>25%) in the middle and lower reaches. The contribution to the hydrochemical compositions of groundwater is relatively small (<25%) for carbonate, silicate and evaporite weathering, but great (>25%) for agricultural activity. This study provides implications for understanding the formation and evolution of water and better watershed water management in that typical endorheic watershed basin and even at larger scales.

Strontium Isotopic Composition as Tracers for Identifying Groundwater Recharge Sources in the Choushui River Alluvial Plain, Western Taiwan

Groundwater is a vital resource in the Chuoshui River alluvial plain (CSAP), a key agricultural area in Taiwan. Understanding groundwater recharge is crucial for sustainable water management amidst changing climatic conditions and increasing water demand. This study investigates the major ion composition, solute Sr concentrations, and 87Sr/86Sr ratios in groundwater and stream water from the Choushui River (CSR) to trace groundwater recharge sources. The Piper diagram reveals that most groundwater samples are of the freshwater Ca–HCO3 type, aligning with the total dissolved solids (TDS) classification. TDS and major ion compositions indicate that groundwater near Baguashan Terrace (BGT) and Douliu Hill (DLH) primarily derives from stream water and rainwater. Na+ and Cl− enrichment in some aquifers of BGT and DLH is attributed to the dissolution of paleo-sea salt and mixing with paleo-seawater from sedimentary porewater. Elevated dissolved Sr concentrations and lower 87Sr/86Sr ratios in these aquifers further support the intrusion of paleo-seawater. Groundwater in the proximal fan shows high TDS due to intensive weathering, complicating the use of TDS as a tracer. Sr isotopic compositions and solute Sr2+ concentrations effectively distinguish recharge sources, revealing that the CSR mainstream primarily recharges the proximal fan and BGT region, while CSR tributaries and rainwater mainly recharge the DLH region. This study concludes that Sr isotopic compositions and solute Sr2+ concentrations are more reliable than TDS and major ion compositions in identifying groundwater recharge sources, enhancing our understanding of groundwater origins and the processes affecting water quality.

Strontium isotopic composition of the Mesozoic sedimentary formations of the southern Central Andes (33°–34°S) and its paleogeographic implications

Strontium isotopic ratios (⁸⁷Sr/⁸⁶Sr) in sedimentary and igneous rocks may provide valuable interpretations that allow constraining the geologic evolution of sedimentary basins. We present a new ⁸⁷Sr/⁸⁶Sr dataset from sedimentary units in the southern Central Andes (33°–34°S)—coupled to available isotopic information of igneous rocks—to examine the paleogeographic evolution of the Andes at the western margin of South America during the Mesozoic. These new data was obtained from shales, limestones and fine-grained sandstones from Mesozoic formations in the Coastal Cordillera and the Principal Cordillera of the main Andes. The new Sr-isotopic data on the Mesozoic sedimentary rocks can be grouped by both rock type and location: a) Continental red sandstones: 0.7038–0.7124; b) Calcareous rocks of the main Andes (Principal Cordillera): 0.7070–0.7081; and c) Calcareous rocks of the Coastal Cordillera: 0.7041–0.7067. The ⁸⁷Sr/⁸⁶Sr signatures in most of the clastic units in both Cordilleras are related to an evolved or enriched magmatic source for clasts and matrix indicating different sources. On the other hand, the Sr-isotopic composition of calcareous rocks differs between the units in the Andean and the Coastal mountain belts: shales and limestones in the Principal Cordillera of the Andes display ⁸⁷Sr/⁸⁶Sr ratios corresponding to the contemporary ocean in the Late Jurassic and Early Cretaceous; whereas the carbonatic units in the Coastal Cordillera do not show a relation with any oceanic signatures. The Sr-isotopic compositions of the Andean carbonatic units in the Principal Cordillera support the interpretation of their marine depositional environment in the paleo Pacific Ocean. In contrast, carbonate rock samples from the formations in the Coastal Cordillera suggest that they formed in brackish-water depositional basins made by topographic highs partially disconnected from the ocean. In the case of clastic rocks, their Sr-isotopic compositions provide insights into the contributions derived from the magmatic arc to the clastic units. Therefore, the Sr-isotopic composition of the sedimentary rocks provides a new dataset which can improve our understanding of the geological evolution of the southern Central Andes.

Geochemistry of forty‐one eclogitic and pyroxenitic mantle xenoliths from the Central Slave Craton, Canada (Ekati Diamond Mine)

AbstractThis article describes a novel dataset on non‐diamondiferous eclogite and garnet pyroxenite xenoliths from four kimberlite pipes of the Ekati Diamond Mine (Central Slave Craton, Canada). Xenoliths brought to the surface by kimberlite eruptions are direct sources of information on the composition and evolution of the Earth's mantle. Eclogite and garnet pyroxenite xenoliths, specifically, are testimony of subduction into, and metasomatism of, the mantle beneath cratons. Furthermore, these rocks are major hosts for diamond and thus an important part of the deep carbon cycle. The sample suite consists of 41 small xenoliths (2–5 cm) recovered from drill cores. The dataset includes major and trace element concentrations for garnet, clinopyroxene and ilmenite, as well as stable oxygen isotope compositions of garnets. Strontium and neodymium isotopic compositions are reported for garnet and clinopyroxene for four samples which were large enough to allow for analysis. Overall, this dataset significantly expands and complements existing datasets on diamondiferous and non‐diamondiferous xenoliths from the Slave Craton in Canada, furthering our understanding of the composition of the Slave subcratonic lithosphere. The dataset includes several samples with rare mineral assemblages, including an olivine‐bearing eclogite as well as ilmenite and apatite‐bearing garnet‐pyroxenites, and thus provides data shedding light on rarely reported compositional nuances in xenolith suites found in kimberlites.

Hydrochemical Characteristics and Evolution of Underground Brine in Lop Nur, Northwestern China

AbstractLop Nur is located at the eastmost end of the Tarim Basin in Xinjiang, Northwestern China. This study reviews the hydrochemical characteristics and evolution of underground brine in Lop Nur, based on analytical data from 429 water samples (mainly brine). It is found that in the NE–SW direction, from the periphery to the Luobei sub‐depression, while the hydrochemical type varies from the sodium sulfate subtype (S) to the magnesium sulfate subtype (M), the corresponding brine in the phase diagram transfers from the thenardite phase (Then) area, through the bloedite phase (Blo), epsomite phase (Eps), picromerite phase (Picro), finally reaching the sylvite phase (Syl) area. As for the degree of evolution, the sequence is the periphery &lt; Luobei horizontally and the overlying glauberite brine &lt; the underlying clastic brine vertically. It is concluded that the oxygen and hydrogen isotopic compositions of the brine have evidently been affected through the effects of evaporation and altitude, as well as the changes in local water circulation in recent years. Boron and chloride isotopic compositions show that the glauberite brine is formed under more arid conditions than the clastic one. The strontium isotopic composition indicates that the Lop Nur brine primarily originates from surface water; however, deep recharge may also be involved in the evolution of the brine, according to previous noble gas studies. It is confirmed that the brine in Lop Nur has become enriched with potassium prior to halite precipitation over the full course of the salt lake's evolution. Based on chemical compositions of brine from drillhole LDK01 and previous lithological studies, the evolution of the salt lake can be divided into three stages and it is inferred that the brine in Lop Nur may have undergone at least two significant concentration‐dilution periods.

The First Data of Strontium Isotopic Composition of Osteological Material from Late Bronze to Early Iron Age Settlements in the Crimea Region

The First Data of Strontium Isotopic Composition of Osteological Material from Late Bronze to Early Iron Age Settlements in the Crimea Region

Sizeable net export of base cations from a Carpathian flysch catchment indicates their geogenic origin while the 26Mg/24Mg, 44Ca/40Ca and 87Sr/86Sr isotope ratios in runoff are indistinguishable from atmospheric input.

Nutrient imbalances may negatively affect the health status of forests exposed to multiple stress factors, including drought and bark beetle calamities. We studied the origin of base cations in runoff from a small Carpathian catchment underlain by base-poor flysch turbidites using magnesium (Mg), calcium (Ca) and strontium (Sr) isotope composition of 10 ecosystem compartments. Our objective was to constrain conclusions drawn from long-term hydrochemical monitoring of inputs and outputs. Annual export of Mg, Ca and Sr exceeds 5-to-15 times their atmospheric input. Mass budgets per se thus indicate sizeable net leaching of Mg, Ca and Sr from bedrock sandstones and claystones. Surprisingly, δ26Mg, δ44Ca and 87Sr/86Sr isotope ratios of runoff were practically identical to those of atmospheric deposition and soil water but significantly different from bedrock isotope ratios. We did not find any carbonates in the studied area as a hypothetical, easily dissolvable source of base cations whose isotope composition might corroborate the predominance of geogenic base cations in the runoff. Marine carbonates typically have lower δ26Mg and 87Sr/86Sr ratios, and silicate sediments often have higher δ26Mg and 87Sr/86Sr ratios than runoff at the study site. Mixing of these two sources, if confirmed, could reconcile the flux and isotope data.

Metallogeny and Genesis of Fault-Filling Barite-Sulfide Veins (Ougnat, Morocco): Petrography, Fluid Inclusion, and Sr-S Isotopic Constraints

The Ougnat Massif of the eastern Anti-Atlas (Morocco) hosts barite and sulfide vein-type deposits of vital economic importance. With over 150 mineralized structures reported in the Ougnat Massif, the ore-bearing ones are predominantly composed of barite, quartz, calcite, and minor portions of sulfides. The mineralized veins are driven by NW-SE and NE-SW to E-W oblique-slip opening faults that cross both the Precambrian basement and its Paleozoic cover. The mineralized structures occur as lenses and sigmoidal veins that follow stepped tension fracture sets oblique to the fault planes. These geometries and kinematic indicators of these structures point to a predominantly normal-sinistral opening in a brittle-ductile tectonic setting. The S isotopic compositions of barite from the Ougnat Massif (+10.8 to +19.5‰) fall mostly within the range of δ34S values of Late Triassic to Jurassic seawater, thus suggesting that some of the SO2− in barite comes from seawater sulfate. This range of δ34S values also corresponds approximately to the hydrothermal barite context. The 87Sr/86Sr ratios of barite, which range from 0.710772 to 0.710816, lie between the radiogenic strontium isotopic compositions of deposition by hydrothermal solutions, and also coincide with the non-radiogenic isotopic signature of Triassic to Jurassic seawater. Based on a fluid inclusions study, the ore-forming fluids were a mixture of two or more fluids. A deep hot fluid with an average temperature of 368 °C leached the granodiorites and volcanic-sedimentary complex of the Ouarzazate Group. This fluid provided the hydrothermal system with most of the Ba, radiogenic Sr, and some of the dissolved S. A second, shallow fluid with an average temperature of 242 °C was derived from Late Triassic to Jurassic seawater. The barite mineralization of the Ougnat Massif constitutes a typical example of vein-type mineralization that occurred along the northern margin of the West African Craton and regionally tied to the central Atlantic opening.

Diversification in subsistence pattern of animal resources in the Hengduan Mountains: Multi‐isotopic evidence of Yingpanshan and Guijiabao site (5300–4000 cal. BP), China

AbstractThe Hengduan Mountains are located on the southeastern edge of the Qinghai‐Tibet Plateau, where farmers began to settle 6000 years ago. Animal husbandry plays a significant role in the sustenance economies of agricultural civilizations. It is unclear how Neolithic people acquired animal resources in the Hengduan Mountains. We explore animal geographical origins and feeding practices using the strontium, carbon, and oxygen isotope composition of tooth enamel at the Guijiabao and Yingpanshan sites during the Neolithic Age in the Hengduan Mountains. Multi‐isotopic evidence demonstrates that animals originate from several different regions with diverse foods. Guijiabao domestic dogs and pigs with a mixed C3/C4 diet share a similarly broad dietary spectrum with humans as enclosed animals, but the other pigs are wild boars with a C3 diet, likely free‐range animals or directly captured as meat resources. Yingpanshan dogs and pigs are both domestic animals with a mixed C3/C4 or C4‐based diet, but pigs with different 87Sr/86Sr ratios are likely raised by dispersed feeding modes. The inhabitants had diverse approaches for obtaining animal resources, including husbandry, hunting, and exchange. Diverse animal subsistence patterns are closely related to the complex geographical environment, reflecting the adaptation of farmers living in the high mountain valley regions.

Mapping of bioavailable &lt;sup&gt;87&lt;/sup&gt;Sr/&lt;sup&gt;86&lt;/sup&gt;Sr in the Southern Trans-Urals

Research subject. Spatial distribution of bioavailable strontium in the South Trans-Urals. Aim. Development and test of a methodology for obtaining a bioavailable strontium map suitable for studying migrations and mobility in the Bronze Age in the Southern Trans-Urals. Methods. Sampling was conducted in 73 loci located in a uniform network in a 25 ± 5 km grid and in 22 additional loci (transects along the intermediate lines in places of complex geological structure). The determination of strontium content was carried out by the ICP-MS method. The strontium isotope composition was measured using an inductively coupled plasma magneto-sector multi-collector mass spectrometer (MC-ICP-MS). Statistical methods included analysis with stem-and-leaf plots; Student’s t-test; ordinary kriging (the mean is unknown) with linear semivariogram; analysis of correlation according to Pearson’s test. Results. The surveyed area is 36 sq. km2. The sample size is 357. Samples for different types have similar mean and median values; the differences occur in the fourth fractional digit. Criterion 1 (n ≥ 0.001) can be used to determine local variability, and Criterion 2 (0.706 &lt; n &lt; 0.716) can be used to assess the origin of ancient individuals, animals, and archaeological objects. The interpolated maps for each sample type were created. All bioavailable strontium maps show similar spatial patterns. Cross-validation revealed areas of the lowest accuracy. Conclusions. The similarity of the distribution of anomalies on the maps of different types suggests the feasibility of the sampling technique. There is a clear tendency for the zones of elevated 87Sr/86Sr values to be associated with the older lithology (0.7106, mean). The lower values (0.7091 ± 0.002) are associated with the younger lithology. Given the complex geological structure and a wide range of rocks in the study area, a positive result is the low differentiation of the zoning of the identified anomalies, which correspond to large structural-formation zones of the Urals. The presented method demonstrates its suitability for studying sublatitudinal migrations of the ancient population of the Southern Trans-Urals.

Geochemical and Isotopic Compositions of Fluorites from the Yama Fluorite Deposit in the Qilian Orogen in Northwest China, and Their Metallogenic Implications

The Yama area is characterized by numerous large-scale fluorite–quartz veins that are located along faults within the widespread Late Devonian–Late Silurian syenogranites in the Tataleng granitic batholith, Qilian Orogen, Northwest China. These fluorite–quartz veins contribute to an important fluorite reserve, but their ore genesis remains unresolved so far. In this study, trace elements, rare earth elements (REEs), and hydrogen, oxygen, and strontium isotopic compositions of fluorites are analyzed. The studied fluorite samples have similar chondrite-normalized REEs, including Y patterns, with relatively strong enrichment in heavy REEs, negative Eu anomalies, strongly positive Y anomalies, and comparably invariable Y/Ho ratios of 41.43–73.79, suggesting a unique hydrothermal genesis. The relatively variable values of δD and δ18O are −77.4‰ to −102.4‰ and −12.7‰ to −4.3‰, respectively, close to the meteoric water line. These fluorites yield relatively invariable analytical 87Sr/86Sr ratios of 0.749089−0.756628 (except for an anomalously high ratio), and their calculated initial 87Sr/86Sr ratios, based on the ore-forming ages provided, are apparently higher than the calculated initial 87Sr/86Sr ratios of syenogranite wall rocks. Collectively, the geochemistry of trace elements, REEs, and stable isotopes (H, O, and Sr) suggests that the ore-forming fluids were of meteoric origin and that the Sr sources were directly derived from the ore-forming fluids themselves rather than syenogranite wall rocks. Finally, it was considered that the Yama fluorite deposit is a fault-controlled hydrothermal vein-type deposit which was possibly related to the evolution of the Paleo-Tethys Ocean in the Permian–Triassic.

Strontium isotope compositions of Late Permian evaporites from the northernmost Thuringian Basin (Germany) indicate continental influence on the marine Zechstein Sea

In the Late Permian Zechstein Sea of Central Europe, up to 2000 m of evaporitic rocks were deposited in at least four consecutive cycles. The age of these evaporitic rocks could not yet be precisely determined, because they are virtually fossil-free and do not contain radiometrically datable volcanic layers. A chemostratigraphic age of the succession can be determined by comparing 87Sr/86Sr ratios of marine gypsum and anhydrite to the worldwide marine strontium evolution curve. Unfortunately, published 87Sr/86Sr data of the Zechstein succession are characterized by frequent outliers towards higher ratios, making an age assignment challenging. The scatter in 87Sr/86Sr ratios might be induced by different processes like the contribution of meteoric water to the brine, in-situ Rb decay, or post-depositional hydrothermal or diagenetic overprint. Here, we present a dataset of 26 new gypsum and anhydrite 87Sr/86Sr ratios from drill cores situated at “Alter Stolberg” in the northernmost Thuringian Basin. Evaporites of the Werra-, Staßfurt-, and Leine cycles were sampled. The close proximity of the drillings allows a very accurate assignment of the stratigraphic position of each sample, so that trends and outliers in 87Sr/86Sr ratios can easily be recognized. While the entire Werra Formation obviously revealed non-marine 87Sr/86Sr ratios, the lowermost 87Sr/86Sr ratios in the Staßfurt and Leine Formations can be assumed to represent marine ratios and allow estimating a chemostratigraphic age of 257‒254 Ma. The combination of the 87Sr/86Sr data with the mineral composition of the samples suggests a contribution of meteoric water, probably river water, to the Zechstein Sea as the main reason for the observed increase in 87Sr/86Sr ratios. Additional in-situ Rb decay, related to the riverine input of clay minerals, cannot be excluded. Modelling the amounts of sea water and meteoric water in the brine indicates that 83‒99% of meteoric water would be necessary to explain the highest 87Sr/86Sr ratios observed in the Werra Formation.Graphical abstract

Strontium and Neodymium Isotopic Signatures in Basalt Glasses of the Mid-Atlantic Ridge, 12°–31° N

This paper presents the new geochemical isotope (Sr–Nd system, H2O, Cl) data obtained for basalt glasses of the Mid-Atlantic Ridge (MAR) sampled from six areas of the MAR axial zone between 31° and 12° N. The data are consistent with the existing ideas about large-scale geochemical segmentation of the MAR. It is shown that samples from predominantly serpentinite segments have a narrower range of variations of strontium isotopic composition (87Sr/86Sr = 0.7027–0.7032) in comparison with samples collected from the areas where the crustal section is dominated by basalts (87Sr/86Sr = 0.7024–0.7041). The variation ranges of the neodymium isotopic composition in these two groups of samples are almost identical (εNd = +4.9 to +10.9 and +5.9 to +11.6 in serpentinite and basalt segments, respectively), although, in general, serpentinite segments have a slightly more enriched composition. The wide variations of the neodymium isotopic composition and increased contents of Cl, H2O, and U, as well as increased K2O/TiO2 and La/Sm ratios, in samples from serpentinites can most probably be related to the participation of different geochemically heterogeneous sources in the magmatism of the MAR axial zone. The influence of enriched plume-type matter cannot be excluded in some segments. The isotopic composition of noble gases may shed light on the subject.

Reconstructing Pleistocene Australian herbivore megafauna diet using calcium and strontium isotopes.

Isotopes in fossil tooth enamel provide robust tools for reconstructing food webs, which have been understudied in Australian megafauna. To delineate the isotopic composition of primary consumers and understand dietary behaviour at the base of the food web, we investigate calcium (Ca) and strontium (Sr) isotope compositions of Pleistocene marsupial herbivores from Wellington Caves and Bingara (New South Wales, Australia). Sr isotopes suggest small home ranges across giant and smaller marsupial herbivores. Ca isotopes in Pleistocene marsupial herbivores cover the same range as those in modern wombats and placental herbivores. Early forming teeth are depleted in heavy Ca isotopes compared to late-forming teeth of a given individual, suggesting a weaning signal. Distinct Ca compositions between taxa can be interpreted as dietary niches. Some niches conform to previous dietary reconstructions of taxa, while others provide new insights into niche differentiation across Australian herbivores. Combined with the small roaming ranges suggested by Sr isotopes, the Ca isotope niche diversity suggests rich ecosystems, supporting a diversity of taxa with various diets in a small area.

Genesis of the Daliuhang Gold Deposit, Jiaodong Peninsula, Eastern China: Constraints from H-O-S-Pb-He-Ar Isotopes, and Geochronology

The Daliuhang gold deposit in the Qipengfu (Qixia–Penglai–Fushan) ore concentration area is a typical gold deposit of medium-low temperature hydrothermal veins. Uncertainties regarding the primary sources of ore-forming fluids, as well as whether host rocks contribute materials to the mineralization of the gold deposits in the Jiaodong Peninsula, are still subject to intense debate. Hydrogen–oxygen isotope results show that atmospheric water is involved in ore-forming fluids. According to the results of the helium–argon isotopes of pyrite, it is hypothesized that the initial fluid source was located in the oceanic crust or upper mantle lithosphere above the Early Cretaceous Paleo-Pacific Plate, as it was subducted into the eastern part of the eastern North China Craton. In situ sulfur isotope results show that high δ34S values characterize the pyrite in the main mineralization period. It is inferred that during the thinning and melting process of the lithospheric mantle, the volatile components enriched in pyrite contributed to the release of δ34S. At the same time, when the fluids ascended to the weak zones, such as fissures of ore-endowed peripheral rocks, the δ34S in the peripheral rocks were extracted, and the two processes acted together to cause high δ34S values to occur. Similarly, the lead and strontium isotopic compositions indicate a crust–mantle mixing attribute of the mineralized material source. The zircon U–Pb age of the ore-hosting granodiorite was 130.35 ± 0.55 Ma, and the Rb–Sr isochron age of the pyrite from the main mineralization period was 117.60 ± 0.10 Ma, which represents the timing of felsic magmatism and gold mineralization, respectively, with at least 10 Ma between the magmatism and mineralization. The magma gradually cooled over time after its formation, and when the granodiorite cooled down to 300 ± 50 °C, the temperature and pressure conditions were most conducive to the precipitation of gold. It is inferred that gold-rich initial mantle fluids with volatile components, rising along tectonically weak zones, such as fractures, underwent fluid phase separation in the fractured position of the granite and extracted the gold from the granodiorite, forming gold deposits.

Use of strontium isotope ratios in potential geolocation of Ajnala skeletal remains: a forensic archeological study.

Stable isotope methods for provenance of unidentified human remains are relatively a newer field of enquiry in forensic archeology. It is of great interest for forensic experts these days. The application of strontium isotope analyses for estimating geolocation of archeological remains is of great interest in bioarcheology and modern forensics. The strontium (Sr) isotope composition of human bones and teeth has been widely used to reconstruct an individual's geo-affiliation, residential mobility, and migration history. Thousands of unknown human remains, reportedly belonging to 282 Indian soldiers of 26th Native Bengal regiment and killed in 1857, were exhumed non-scientifically from an abandoned well situated underneath a religious structure at Ajnala (Amritsar, India). Whether these remains belonged to the individuals, local or non-local to the site, was the important forensic archeological question to be answered by doing their thorough forensic anthropological examinations. In the present study, 27 mandibular teeth (18s molars, 6 first molars, and 3 premolars) collected from the Ajnala skeletal assemblage were processed for strontium isotope analysis, and the measured ratios were compared with published isotope baseline data to estimate the locality status of these remains. The Sr isotopic values were concentrated in the range of 0.7175 to 0.7270. The comparative analysis of isotopic ratios revealed that most individuals buried in the Ajnala well have 87Sr/86Sr values close to the river as well as groundwater of the Gangetic plain (less radiogenic 87Sr/86Sr ~ 0.716); most likely originated near Varanasi (Uttar Pradesh, India) region, whereas the individuals with higher 87Sr/86Sr ratios (~ 0.7200) probably resided in the West Bengal and Bihar areas where the river as well as groundwater of the Gangetic plain is relatively more radiogenic. Thus, the strontium isotope results reveal that the Ajnala individuals did not grow up or live in the Amritsar region during their childhood, and this observation complemented the previous forensic anthropological and molecular findings. There is very little Indian data on the bioavailable strontium, so the inferences from the present study estimating Sr isotope abundances are expected to provide baseline data for future forensic provenance studies that will contribute to the global efforts of mapping Sr isotope variations by the isotope community.

Petrological, Geochemical and Chronological Characteristics of Dolomites in the Permian Maokou Formation and Constraints to the Reservoir Genesis, Central Sichuan Basin, China

The Middle Permian Maokou Formation in the Sichuan Basin has huge resources and is an important target for natural gas exploration. In recent years, significant exploration breakthroughs have been made in the dolomite field of member Mao-2 in central Sichuan, and the gas production of several wells has exceeded 1 × 106 m3/d, indicating promising prospects for exploration. However, the origin of the dolomite reservoir in member Mao-2 remains ambiguous, which restricts the accurate prediction of favorable reservoirs. This study focuses on drilling in the Hechuan area as its research object, by using a detailed description of the cores from member Mao-2 of seven wells; samples were selected for tests of the degree of dolomite cation ordering, stable carbon and oxygen isotopic compositions, strontium isotopic composition, rare earth elements, LA-ICP-MS element mapping and U-Pb dating. It is clarified that: (1) The crystalline dolomite of member Mao-2 in the Hechuan area is the main reservoir rock, and the heterogeneous vugs and fractures are the main reservoir space. The dolomite in member Mao-2 has been characterized by a low degree of cation ordering value (avg. 0.59), with values of δ13C (avg. 3.87‰), δ18O (avg. −7.15‰) and 87Sr/86Sr (avg. 0.707474) having similar geochemical characteristics to Middle Permian seawater; the REEs normalized distribution patterns have similar characteristics to limestone; and the U-Pb age (261.0~262.0 Ma) corresponds to the age in the Capitanian stage of the Permian Guadalupian Series. (2) Petrological studies show that member Mao-2 has vertical karstification zonation characteristics; syngenetic karstification controls the formation of a large-scale fracture-cave system in the phreatic zone; the dolomitization of sediment in the fracture-cave system occurred during the penecontemporaneous period with locally restricted seawater. (3) The main controlling factors of the reservoir were syngenetic karstification, early dolomitization and hydrothermal dissolution related to Emei taphrogenesis. The research results are of great significance for dolomite reservoir prediction; the highlands of paleogeomorphology with syndepositional faults are favorable areas for dolomite reservoirs.

C- AND Sr-ISOTOPE CHEMOSTRATIGRAPHY OF THE UPPER PROTEROZOIC – LOWER CAMBRIAN TRANSITIONAL DEPOSITS IN THE LENA-ANABAR TROUGH (NORTHEASTERN SIBERIAN PLATFORM)

Studies have been made of the carbon and strontium isotope composition in carbonate sediments of the Khorbusuonka group and Kessyusa formation corresponding to the Upper Vendian in deep Khastakhskaya-930 and Burskaya-341-0 boreholes at the northeastern margin of the Siberian Platform. The maximum δ13С values in carbonates of the Turkut and Kessyusa formations in the Khastakhskaya-930 borehole are +7.0...+7.4 %, while the minimum 87Sr/86Sr ratios are as low as 0.7079. Such isotope-geochemical characteristics suggest that these formations are younger (Tommotian) or older (early Vendian) than it was supposed and allow for the possibility of alternatives to their regional correlation with the Burskaya-341-0 borehole and Olenek uplift sections. The deposition of sediments of the age considered, more intensive than in the adjacent regions, may be indicative of rift-related extension settings.