Sr Isotope Systematics Research Articles

Age and sources of low-sulfide gold-quartz mineralization of the Karalon gold ore field (North Transbaikalia, Russia): results of isotope-geochemical (Rb-Sr and Pb-Pb) studies

The article presents the results of studying the Rb–Sr isotope system of ore-bearing granitoids, apogranite metasomatites and hydrothermalites of the Verkhnekaralonskoye gold deposit, as well as the Pb-Pb isotope system in galena of the gold-quartz low-sulfide mineralization of the Karalonskoye gold ore field. Three groups of ore objects with different Pb isotopic compositions of galena associated with varying contributions from mantle and ancient crustal sources have been identified. The isotope characteristics of Pb in galena of the Verkhnekaralonskoe deposit indicate its genetic relationship with ore-bearing juvenile granites, whose age of ~ 600 Ma may be close to the age of the earliest stage in the formation of gold–quartz mineralization. The ancient crustal source is common for the leading gold deposits of Northern Transbaikalia and is characterized by the parameters of the continental crust of the Siberian craton at a time of 500–600 Ma. The rearrangement of the Rb–Sr system in the studied rocks and minerals of the Verkhnekaralonskoe deposit and the redistribution of Pb isotopes in galena of the Vodorazdelnaya ore zone of the Karalonskoe ore field at the turn of 290–250 Ma have been established. Isotope data show that in the geological history of the Verkhnekaralonskoe deposit and the Karalonskoe ore field, the formation of gold mineralization had a long multi-stage character and was accompanied by the regeneration of primary ore concentrations.

δ26Mg, δ44Ca and 87Sr/86Sr isotope ratios constrain Mg and Ca input–output mass balances in a heavily acidified headwater catchment

A Central European catchment underlain by base-poor orthogneiss was studied using mass budgets and Mg–Ca–Sr isotope systematics. For 50 years, the catchment received large amounts of partly soluble dust from a nearby cluster of coal-burning power plants, while suffering from acid rain and severe spruce die-back. Our objective was to investigate to what extent anthropogenic dust contributes to Mg and Ca in runoff and to identify fractionations affecting Mg and Ca isotope composition of 13 ecosystem pools and fluxes. We hypothesized that if Mg and Ca runoff fluxes were significantly larger than their atmospheric inputs, Mg and Ca isotope ratios in runoff would converge to those of bedrock Mg and Ca. This relationship could be obscured by isotope fractionations. Strontium characterized by negligible isotope fractionations served as a Ca proxy. There was a strong positive correlation between Mg and Ca fluxes via spruce throughfall and catchment runoff. Monitoring of rainfall, canopy throughfall and runoff fluxes revealed a 20-, 15- and 15-fold excess of Mg, Ca and Sr in runoff, respectively, compared to atmospheric deposition fluxes. This sizeable excess per se would indicate predominance of geogenic base cations in runoff. The behavior of Mg and Ca isotopes was de-coupled. Petrographic study indicated that 92% of bedrock Mg was bound to easily dissolving biotite, 97% Ca was present in plagioclase, and nearly all Sr was in orthoclase. While Mg isotope ratios in bedrock and runoff were indistinguishable, corroborating predominantly geogenic Mg in runoff, Ca and Sr isotope ratios in bedrock and runoff were significantly different, consistent with a non-negligible contribution of atmospheric Ca and Sr to runoff. Previous study of sites underlain by felsic rocks indicated that the δ44Ca value of apatite was often higher than the δ44Ca value of plagioclase. Should weathering of apatite and/or plagioclase preferentially release Ca that is isotopically heavier than bulk rock, the geogenic Ca source at JEZ would converge to the mean δ44Ca value of runoff. Calcium isotope data would then become more consistent with a major role of geogenic Ca in JEZ runoff indicated by mass balance data.

Geochemical Study of the Osumi Granodiorite, Southwestern Japan

The Osumi Granodiorite, located on the Osumi Peninsula in southwest Japan, is an example of outer zone granites that were formed during a limited period (13–15 Ma) in response to the subduction of the Philippine Sea Plate. This event, which is linked to the separation of southwest Japan from continental Asia, resulted in unique igneous activity. The Osumi Granodiorite is the largest Miocene granite body in the region. It intrudes into the Mesozoic to Paleogene accretionary complex of the Shimanto Belt and affects contact metamorphism. Despite considerable research on the Osumi Granodiorite, limited geochemical studies, especially on trace and rare earth element (REE) analyses, have been conducted. Furthermore, there are insufficient data on the Rb–Sr isotopic system, leaving the formation process unclear. This study presents whole-rock geochemical and Rb-Sr isotopic data to investigate the petrogenesis of the Osumi Granodiorite. The results suggest a common magma origin for this pluton, as indicated by linear trends on the Harker diagrams and similar REE patterns. The presence of a relatively large Eu anomaly implies formation under a reducing environment. The AKF diagram indicates predominant contamination by pelitic rocks of the Shimanto Belt during magma formation. The Rb–Sr whole-rock isochron diagram and SrI–1000/Sr diagram suggest that the Osumi Granodiorite body was formed by heterogeneous assimilation of magma into the Shimanto Belt. Furthermore, the whole-rock isochron age is 64.3 Ma, which differs by approximately 50 My from the previously reported biotite K–Ar age (14–22 Ma). This age is considered to be a pseudo-isochron age, rather than the consolidation age. During the middle Miocene, the compressive stress field in the outer zone south of the Butsuzo Tectonic Line made it difficult for magma to rise. As a result, it reacted with the sedimentary rocks of the Shimanto Belt to various degrees. The Osumi Granodiorite underwent magma differentiation upon intrusion into the Shimanto Belt. It subsequently ascended, cooled, and interacted with pelitic rocks under stable geological conditions.

Petrogenesis and Geodynamic Evolution of the Archean Shawmere Anorthosite Complex and Associated Gneisses, Kapuskasing Uplift, Superior Province, Canada

Abstract In this study, we integrated extensive field, petrographic, whole-rock major and trace element, and Nd–Pb–Sr–O isotope, and zircon U–Pb ages, trace element and Lu–Hf isotope data from the Neoarchean Shawmere Anorthosite Complex and surrounding gneisses to unravel their petrogenetic origin and tectonic history. The ~2765 Ma Shawmere Anorthosite Complex is interpreted to have been emplaced into a sequence of interlayered greywacke and basalt deposited in an intra-continental arc rift system above a north-dipping subduction zone. The complex consists mainly of anorthosite, leucogabbro, gabbro, and hornblendite that were emplaced as several batches of magmas and crystal mushes originating from sub-arc mantle sources. In contrast to the previous studies, our field and petrographic data suggest an igneous origin for the most hornblende in the complex, implying hydrous parental magmas. A hydrous magma origin is also consistent with the high-anorthite content (mostly 70–90%) of the plagioclase in the complex. Percolation of hydrous basaltic melts through gabbroic cumulates in crustal magma chambers led to extensive (>50%) replacement of igneous clinopyroxene by igneous hornblende. Continued subduction resulted in the closure of the intra-arc rift system and the intrusion of the complex by tonalite, granodiorite and diorite between 2765 and 2680 Ma in an Andean-type margin. The complex and surrounding gneisses underwent hornblende granulite-facies metamorphism mainly between 2680 and 2620 Ma, overlapping with mid-crustal east-west extension between 2660 and 2640 Ma. The granulite-facies metamorphism is recorded by the replacement of hornblende, plagioclase and clinopyroxene by garnet and the development of a garnet-orthopyroxene-plagioclase metamorphic assemblage with a granoblastic texture. Tectonic rebounding of mid-crustal rocks to upper crustal levels after 2620 Ma led to the formation of an extensive network of extensional fractures and retrograde metamorphism. Migration of CO2-rich hydrous fluids along the extensional fractures and grain boundaries resulted in the precipitation of many metasomatic minerals mainly at the expense of hornblende and plagioclase, including epidote, clinozoisite, tremolite, actinolite, paragonite, margarite, titanite, quartz, calcite, sillimanite, dolomite, and chlorite. Prevalent replacement of hornblende by garnet during prograde metamorphism and metasomatic replacement of hornblende and plagioclase by retrograde mineral assemblages disturbed the Sm–Nd, U–Th–Pb, and Rb–Sr isotope systems.

Uranium-series and strontium isotope systematics in soil carbonates from dryland Critical Zones: Implications for soil inorganic carbon storage and transformation

Soil carbonates are dominantly present in dryland Critical Zone (CZ) and their formation could lead to important long-term carbon sequestration in arid to semiarid soils if the Ca ions were derived from silicate weathering or other non-carbonate sources. In managed CZ systems such as agricultural areas converted from natural drylands, irrigation has profound effects on the dryland CZ inorganic carbon storage, especially by modifying dissolution and precipitation dynamics of soil carbonates via controls of irrigation intensity and water chemistry, soil properties, and hydrological flow paths. These processes could lead to transformation of inorganic carbon in soils and groundwater aquifers underneath drylands. One key knowledge gap in studying soil carbonates from managed dryland CZ systems is to detect the formation of soil carbonates under irrigated conditions and distinguish them effectively from soil carbonates formed under natural conditions.Here, we explore the potential of using U-series and strontium isotopes to investigate the formation timescales and conditions of soil carbonates in both natural and managed dryland CZ in Chihuahua Desert of American Southwest. We obtained new U-series and Sr isotope ratios from mature stage V natural soil carbonates in the Jornada Basin of southern New Mexico and compared to previously published U-series and Sr isotope results for younger Jornada soil carbonates as well as irrigation impacted soil carbonates from the Rio Grande floodplains in west Texas. Specifically, we applied the U-series dating method (238U-234U-230Th) to estimate the timescales of soil carbonate formation under both natural climatic conditions and impacts of modern agriculture irrigation. In addition, we showed that the initial (234U/238U) activity ratios recorded in these soil carbonates reflect the systematic changes of soil infiltration rates in both natural and managed dryland CZ. We also utilized Sr isotope ratios (87Sr/86Sr) in soil carbonates, dust, and irrigation water to trace the Ca sources in soil carbonates from natural and managed dryland CZ. Soil carbonates from both settings were characterized by slightly radiogenic 87Sr/86Sr ratios, consistent with their potential of long-term carbon storage in drylands.U-series and Sr isotope systematics characterize important differences in soil carbonates from natural and managed dryland CZ with respect to their Ca sources, timescales of carbonate formation and transformation, and availability of soil moisture. Soil carbonates formed, accumulated, and transformed in natural drylands with long time scales but under irrigated arid agricultural areas its formation is significantly modified by irrigation and other agriculture practices, with implications for long- and short-term inorganic carbon sequestration in both systems of drylands.

Implementation and experience of using methods for analyzing the isotopic composition of Sm and Nd, Rb and Sr in rock samples at the Geoanalitik Center for Collective Use

Research subject. AGV-2 and BHVO-2 geochemical reference materials for studying the Sm, Nd and Rb, Sr isotope systems along with various rocks and mineral samples. Materials and Methods. An analysis of the isotopic composition of Sm, Nd and Rb, Sr was carried out using Neptune Plus and Triton Plus mass spectrometers. Aim. To implement analytical techniques for the isotopic composition of Sm and Nd, Rb, and Sr in various rock and mineral samples using two types of multicollector mass spectrometers – inductively coupled plasma NeptunePlus and thermal ionization TritonPlus (Thermo-Fisher), as well as a description of the procedure of processing experimental data and the experience in using techniques at the “Geoanalitik” shared research facilities of the IGG UB RAS for the period 2015-2023. Results. The analytical techniques implemented included (1) column chromatography using various ion-exchange resins, optimised for the ratio of labour costs/quality of analytical results; (2) the measurement of isotope ratios using two types of mass spectrometers; (3) the correction of mass bias of isotope ratios and the determination of Sm and Nd, Rb, and Sr concentrations by the isotope dilution method using 149Sm+150Nd and 85Rb+84Sr spikes. Testing of the techniques was carried out using the AGV-2 and BHVO-2 geochemical reference materials; their metrological characteristics were presented. When using TritonPlus, the reproducibility (BHVO-2, n=60) of measurements of 143Nd/144Nd, 147Sm/144Nd isotope ratios and Sm and Nd concentrations are ±0.000020, ±0.0004, ±1.3 and ±0.4, respectively; indicators of correctness of determining the ratios 143Nd/144Nd and 147Sm/144Nd – 0.001 and 0.25% and concentrations of Sm and Nd – 2%; the reproducibility (BHVO-2, n=63) of measurements of 87Sr/86Sr, 87Rb/86Sr isotope ratios and concentrations (Rb and Sr) are ±0.0025%, ±1.5%, ±2%, respectively. The uncertainty of a single measurement of the 143Nd/144Nd and 87Sr/86Sr isotope ratio, represented by the standard error of the average single measurement in the sample, does not exceed 0.0025%. Conclusions: the results obtained for the geochemical reference materials are in satisfactory agreement with those provided in the GeoReM database, as well as with the certified values provided by the United States Geological Survey (USGS). The described analytical techniques are used at the “Geoanalitik” shared research facilities of the IGG UB RAS to analyse various rock and mineral samples. The work presents a number of experimental results obtained, which are subsequently used in geochronological applications.

Sr–Nd Isotopic Evidence of a Heterogeneous Magmatic Source of Alkaline–Carbonatite Rocks of the Odikhincha Alkaline–Carbonatite Massif (Maimecha-Kotui Province, Siberia)

This study focuses on the igneous rocks composing the Odikhincha massif. The massif is typical ring alkaline–ultrabasic massif with carbonatites, second largest in the Maimecha-Kotui province. The Sr-Nd isotopic values of the traps of the Arydzhang Formation and the host dolomites were also determined for comparison. The Rb–Sr isotope system of phlogopite and calcite from the Od-16-19 carbonatite of the Odikhincha massif is disturbed; the obtained age on the mineral isochrone (245 ± 3 Ma) is close to the time of formation of the Siberian traps and rocks of the ultrabasic–alkaline Maimecha-Kotui complex, but the large scatter of analytical points (MSWD = 22) does not allow this date to be considered as reliable. The disturbance of the isotope system is probably related to the fact that the strontium isotope ratio in the fluid was not constant during autometasomatic phlogopitization of carbonatite. The U–Pb isotopic system of titanite and perovskite from the same carbonatite sample Od-16-19 also appeared to be disturbed, since data points formed discordia. The U–Pb age obtained for titanite and perovskite are 244 ± 5 Ma (MSWD = 1.8) and 247 ± 18 Ma (MSWD = 4), respectively. Apparently, the age values provided by the two isotopic systems (245 ± 3 Ma by Rb–Sr and 247 ± 18 and 244 ± 5 Ma by U–Pb) are consistent with each other and reflect the time of metasomatic processes, i.e., phlogopitization and iolitization. Rb–Sr and Sm–Nd isotope data for ultrabasic–alkaline intrusive rocks with carbonatites of the Odikhincha massif and volcanics of the Arydzhang Formation indicate an enriched, relative to the composition of the convecting mantle, isotopically heterogeneous source of their parent melts. This source could be a combination of ultrabasic mantle rocks and rocks of basic composition (basites). The latter played the role of an enriched component. No signs of contamination of the melts with the host sedimentary rocks in situ were found, however, variations of Sr and Nd isotopic ratios in the rocks of the Odikhincha massif may indicate that during the introduction of deep magmas their interaction and substance exchange with the surrounding rocks of the lithosphere continued up to complete solidification of the melts, as indicated by the nature of local isotopic heterogeneity within the Odikhincha intrusion.

Sr–Nd Isotopic Evidence of a Heterogeneous Magmatic Source of Alkaline–Carbonatite Rocks of the Odikhincha Alkaline–Carbonatite Massif (Maimecha-Kotui Province, Siberia)

This study focuses on the igneous rocks composing the Odikhincha massif. The massif is typical ring alkaline–ultrabasic massif with carbonatites, second largest in the Maimecha-Kotui province. The Sr-Nd isotopic values of the traps of the Arydzhang Formation and the host dolomites were also determined for comparison. The Rb–Sr isotope system of phlogopite and calcite from the Od-16-19 carbonatite of the Odikhincha massif is disturbed; the obtained age on the mineral isochrone (245 ± 3 Ma) is close to the time of formation of the Siberian traps and rocks of the ultrabasic–alkaline Maimecha-Kotui complex, but the large scatter of analytical points (MSWD = 22) does not allow this date to be considered as reliable. The disturbance of the isotope system is probably related to the fact that the strontium isotope ratio in the fluid was not constant during autometasomatic phlogopitization of carbonatite. The U–Pb isotopic system of titanite and perovskite from the same carbonatite sample Od-16-19 also appeared to be disturbed, since data points formed discordia. The U–Pb age obtained for titanite and perovskite are 244 ± 5 Ma (MSWD = 1.8) and 247 ± 18 Ma (MSWD = 4), respectively. Apparently, the age values provided by the two isotopic systems (245 ± 3 Ma by Rb–Sr and 247 ± 18 and 244 ± 5 Ma by U–Pb) are consistent with each other and reflect the time of metasomatic processes, i.e., phlogopitization and iolitization. Rb–Sr and Sm–Nd isotope data for ultrabasic–alkaline intrusive rocks with carbonatites of the Odikhincha massif and volcanics of the Arydzhang Formation indicate an enriched, relative to the composition of the convecting mantle, isotopically heterogeneous source of their parent melts. This source could be a combination of ultrabasic mantle rocks and rocks of basic composition (basites). The latter played the role of an enriched component. No signs of contamination of the melts with the host sedimentary rocks in situ were found, however, variations of Sr and Nd isotopic ratios in the rocks of the Odikhincha massif may indicate that during the introduction of deep magmas their interaction and substance exchange with the surrounding rocks of the lithosphere continued up to complete solidification of the melts, as indicated by the nature of local isotopic heterogeneity within the Odikhincha intrusion.

Metamorphic P–T conditions, in‐situ LA–ICP–MS biotite–muscovite Rb–Sr geochronology and tectonic implications of two‐mica–quartz schist from the Kuanping Group in the North Qinling Orogenic Belt

The Kuanping Group is an important lithotectonic unit in the North Qinling Tectonic Belt, which has experienced metamorphism from greenschist to high amphibolite facies and is of great significance in defining the orogenic process of the Qinling Orogenic Belt. This study presents the results of petrology, geothermobarometry, phase equilibrium modelling, in‐situ laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS) biotite–muscovite Rb–Sr analysis, for the two‐mica–quartz schist of the Kuanping Group in the Hongtuling and Heihe areas. These results are employed to better understand their metamorphic P–T conditions and ages, as well as geological implications. Garnet‐bearing two‐mica–quartz schist in the Hongtuling area records a clockwise P–T trajectory on the basis of phase equilibrium modelling, with peak P–T conditions of ~600°C and ~0.85 GPa. In addition, the Ti‐in‐biotite thermometry yielded metamorphic temperature conditions of ~578°C–580°C and ~590°C–596°C for the garnet‐bearing two‐mica–quartz schist from the Hongtuling area and the two‐mica–quartz schist from the Heihe area, respectively. These results indicate that metamorphic temperature conditions in both areas are higher than the closure temperature of the Rb–Sr isotopic system of muscovite and biotite. In‐situ LA–ICP–MS biotite and muscovite Rb–Sr analyses yielded three groups of isochron age, i.e., ca. 410 Ma, ca. 360 Ma and ca. 320–300 Ma. On the basis of previously published data and the data in this study, the Kuanping Group underwent ca. 440 Ma regional metamorphism in the NQB, retrograde cooling at ca. 410–360 Ma due to exhumation and ca. 320–300 Ma tectonothermal overprinting.

The Accumulation of the REE by Bacterial Fe Oxyhydroxide

The current study was focused on Fe oxyhydroxides from the north-western part of the East-European platform. Modern-day Fe oxyhydroxides of bacterial origin demonstrate an enhanced concentration of rare earth elements (up to 1200 ppm), compared to samples without iron bacteria. The 143Nd/144Nd ratio in bacterial Fe oxyhydroxide has the value from 0.511532 to 0.512588 and corresponds to the geochemical signature of the waters, oxyhydroxides precipitated from. Samples of iron hydroxides from Quaternary and recent continental ore deposits with different Nd and Sr isotope composition were used for the laboratory reduction of Fe3+ up to emergence of magnetite (T ~ 1000°C). 143Nd/144Nd and 87Sr/86Sr ratios in the newly formed mineral phases show insignificant discrepancy with parent iron ore. The persistency of Sm–Nd and Rb–Sr isotope systems in the process of bog iron ore experimental melting permits it’s applying to paleoenvironment reconstructions and archaeometry.

Massive influence of Himalayan source on sedimentation along northern Indian peninsular basin

A 39 m long sediment core (MD161-19) spanning 320 ka, collected from the intermediate water depths of (1480 m) of Mahanadi offshore was subjected to provenance analyses using Sr and Nd isotope systematics. The Sr–Nd isotope ratios of MD161-19 fall on the mixing line defined by Ganga and Brahmaputra main stem averages. Strontium and Nd isotope ratios along with Fe/Al ratio clearly show the predominance of Himalayan sediments in the study area. The significant temporal variations in the Sr–Nd isotope ratios observed for the entire depositional age (320 ka) may be attributed to changes in the relative sediment contribution by Ganga and Brahmaputra river systems draining terrains with contrasting Sr–Nd isotope ratios. The temporal geochemical profiles coupled with precipitation profile show that wet-phases during stadials led to enhanced erosion of the trans-Himalayan batholiths (THB) rocks (characterized by high εNd values) possibly due to glacial expansion in the higher reaches of the Brahmaputra catchment. The warm interstadials coupled with enhanced precipitation are accompanied by a shift towards lower εNd values which may be attributed to extensive erosion of the Ganga catchment area comprising rocks characterized by lower εNd values and diminished THB contribution due to lack of glacial influence.

Carbonatisation and overprinting mineralisation in Siah-Kamar porphyry molybdenum deposit, NW Iran

The Siah-Kamar porphyry Mo deposit (SKD) is located at the north-western termination of the Urumieh-Dokhtar magmatic arc and it is the only known porphyry Mo ore reserve in Iran. The SKD formed in two main mineralisation stages, at ~33–32 Ma (late-stage, disseminated) and ~ 29–28 Ma (late-stage, high-grade), within a context of a long-lived magmatism. We integrate results from the whole-rock geochemistry, the OC stable and Sr isotope systematics across the mineralised alteration zones with the available drilling data (ore element concentration) to define the ore-forming processes leading to Mo enrichment in the SKD. Our investigation shows that CO2 bearing magmatic fluids had the major role in both early and late-stage mineralisation. The Mo shows positive correlation with SiO2 content but a clear negative correlation with W, Cu, and S, due to a delayed precipitation of Mo during the early-stage mineralisation. The released fluids from the new acidic magmas and subsequent fluid-rock interaction in an open-system, primarily assisted by brittle fracturing, and accompanied by cooling and mixing with various amounts of meteoric water and fluid neutralisation, was responsible for the selective ore depletion and Mo-ore enhancement during carbonatisation along structurally-controlled pathways.

Zircon U–Pb geochronology and Sm–Nd and Rb–Sr isotope systematics of Neoproterozoic granitoïds from Bou Azzer (Anti-Atlas - Morocco): The obduction trigger of the central Anti-Atlas terrane

This study presents new U–Pb zircon ages for the Neoproterozoic granitoids of the Bou Azzer inlier at the central part of the Anti-Atlas chain (Morocco), in the northwestern edge of the West African Craton (WAC). Analyzes of zircon grains yield the following ages: 658 ± 3 Ma for Ait Ahmane pluton, 647 ± 5 Ma for Bou-Izbane intrusion, 656 ± 3 Ma for Bou Azzer quartz-diorites, 583 ± 12 Ma in the Oustrate intrusion and 644 ± 4 Ma for the Ait Ahmane leucogranite. These ages confirm a major magmatic event between 640 and 660 Ma contemporaneous with the obduction of oceanic crust marking the formation of the ophiolites of Bou Azzer and Sirwa. The emplacement of granitoids would have led to a decrease in the density of the oceanic crust and triggered the process of obduction. The granitoids display the geochemical features of volcanic arc magmas and have positive initial ϵNd (+4.67 to +6.57) and low initial 87Sr/86Sr (0.7002–0.7055). The quartz-diorite group displays young Depleted Mantle Model (TDM) ages that range from 904 to 1065 Ma. The leucogranites have younger TDM of 869–884 Ma. These new data attest to their juvenile nature and the absence of any crustal contribution. The NNW-SSE extended inlier band of Bou Azzer - Sirwa constitutes an exotic terrane of Neoproterozoic age and of a juvenile nature wedged between the SW and NE domains, respectively, formed by or surmounting a Meso-Paleoproterozoic or even Archean basement. The Bleida granodiorite, dated at 559 ± 4, displays older U–Pb ages from inherited zircon cores at 1234, 1748 and 2085 Ma. The Bleida granodiorite was emplaced during a later magmatic episode that belongs to the Ouarzazate Group, generated during the post-collisional metacratonic evolution of the northern edge of the West African craton.

An investigation of factors affecting high-precision Sr isotope analyses (87Sr/86Sr and δ88/86Sr) by MC-ICP-MS

The stable strontium (Sr) isotope system is being increasingly utilized to move forward our understanding of environmental, geological, and cosmological processes. Two analytical techniques are commonly used to measure stable Sr isotopes: 1) double-spike thermal ionization mass spectrometry (DS-TIMS) and 2) Zr-doped sample-standard bracketing multi-collector inductively coupled plasma mass spectrometry (Zr-doped SSB via MC-ICP-MS). Relative to DS-TIMS, Zr-doped SSB via MC-ICP-MS allows simultaneous determination of both 87Sr/86Sr and 88Sr/86Sr ratios, increasing measurement efficiency and sample throughput. However, several factors limit the analytical precision and accuracy of this technique, including matrix effects and potential intra- and inter-session offsets of measured isotope ratios. In this study, we evaluate potential causes for the observed offsets. We performed a series of experiments to assess the effect of different solution matrices and sources of contamination on Sr isotope measurements and to explore potential underlying mechanisms. Our tests show that incomplete Sr recovery during chromatographic separation, mismatches of Sr and Zr concentrations and acid molarity between samples and bracketing standards, and cation contamination all affect the precision and accuracy of Sr isotope measurements. We present evidence that analyses using our recommended updated preparation procedure for Zr-doped SSB via MC-ICP-MS can achieve a long-term reproducibility (2σSD: 87Sr/86Sr = ±0.000015 and δ88/86Sr = ±0.03 ‰) comparable to that of DS-TIMS.

Sr, Nd, Pb, and Os Isotope Systematics and Derivation of Mesozoic Plume-Related Basalts of Antarctica: Karoo-Maud and Kerguelen Plume Realm

The study of Re–Os isotopic systematics of the Mesozoic magmas in East Antarctica and its comparison with Sr–Nd–Pb–Os published data allowed us to reveal the main features of Antarctic magmatism associated with the activity of the Karoo–Maud (Dronning Maud Land (DML), Karoo and Ferrar provinces) and the Kerguelen (Lambert rift area) plumes. It is shown that a melt source of the 180-Ma Karoo–Maud plume could be enriched lithospheric mantle. Variations of the 187Os/188Os ratio in the range of 0.1242–0.1426 characterize almost all types of melts in the Karoo and DML provinces, including both high- and low-Ti magmas as well as high-Mg ferropicrites produced by melting of mantle pyroxenite. This observation is consistent with previous assumption that magmas derived from pyroxenite mantle at the initial stage of plume impact represented melts of deep lithospheric fragments of ancient Gondwana paleocontinent that were entrapped by plume. Thereby, mantle heterogeneity recorded in the Nd–Pb–Sr isotopic compositions of the basalts is not expressed in the systematic variations of Re–Os isotope system. The magmatic source of the basalts of the Ferrar province differs from the source of Mesozoic magmatism in the Karoo and DML provinces by great variations in the 187Os/188Os ratio: from 0.1 to 0.31, and by the lower osmium contents, with limited variations of other isotopic systems, indicating an admixture of enriched EM-II source. This is consistent with inferred subduction reworking of the mantle of the western Antarctic margin (Sushchevskaya et al., 2022). Ultramafic picritic magmas from the Lambert Glacier area are characterized by a radiogenic osmium isotopic composition: 187Os/188Os 0.1582–0.2388. Source of these magmas could be ancient depleted mantle, which later experienced mantle metasomatism due to the multiple interactions with fluid-saturated melts. Picritic melts of the paleorift zone of the Lambert Glacier are close to a magma source of the Karoo and DML provinces in terms of Sr-Nd isotopic composition, but differ in more radiogenic lead.

Sr, Nd, Pb, and Os Isotope Systematics and Derivation of Mesozoic Plume-Related Basalts of Antarctica: Karoo-Maud and Kerguelen Plume Realm

Sr, Nd, Pb, and Os Isotope Systematics and Derivation of Mesozoic Plume-Related Basalts of Antarctica: Karoo-Maud and Kerguelen Plume Realm

Effects of Mantle Hybridization by Interaction with Slab Derived Melts in the Genesis of Alkaline Lavas across the Back-Arc Region of South Shetland Subduction System

AbstractLate Miocene to Late Pleistocene alkaline lavas in the northernmost part of the Antarctic Peninsula and its off-lying islands are the latest stage of magmatic activity that took place in response to lithospheric extension in the back-arc region of the South Shetland subduction system. The alkaline magmatism occurred much later than the main pulse of Cretaceous arc magmatism and generated basaltic extrusive rocks during several sub-aqueous/sub-glacial and sub-aerial eruption periods. The suite consists primarily of alkali olivine basalts with oceanic island basalt (OIB)-like trace element signatures, characterized by elevated highly to less incompatible element ratios compared to MORB. The samples have higher 87Sr/86Sr (0.70301–0.70365), and lower 143Nd/144Nd (0.51283–0.51294) and 176Hf/177Hf (0.28291–0.28298) than depleted MORB mantle. Their lead isotope ratios vary within a limited range with 206Pb/204Pb, 207Pb/204Pb, 208Pb/204Pb ratios of 18.797–18.953, 15.577–15.634, and 38.414–38.701, respectively. Sr, Nd, Hf and Pb isotope systematics suggest involvement of diverse source materials in the genesis of the alkaline magmas. Evaluation of radiogenic isotope and trace element data indicates that the source of the alkaline melts had a complex petrogenetic history, reflecting the effects of mantle hybridization along the slab mantle interface through interaction of mantle wedge peridotites with volatile-bearing, siliceous melts produced by melting of subducted sediments and basaltic oceanic crust. Hf-Nd isotope and trace element projections further demonstrate that the metasomatizing melt was likely generated by eclogite partial melting at sub-arc to post-arc depths, in equilibrium with a garnet-bearing residue and involved breakdown of high field strength elements (HFSE) retaining phases. Consumption of metasomatic amphibole during partial melting of hybridized peridotite at the wet solidus appears to have had a significant effect on the final melt compositions with high HFSE, Na and H2O contents.

Rare earth elements and neodymium and strontium isotopic constraints on provenance switch and post-depositional alteration of fossiliferous Ediacaran and lowermost Cambrian strata from Arctic Norway

The Digermulen Peninsula in northeastern Finnmark, Arctic Norway, comprises one of the most complete Ediacaran–Cambrian transitions worldwide with a nearly continuous record of micro- and macrofossils from the interval of the diversification of complex life. Here, we report on the provenance and post-depositional alteration of argillaceous mudstones from the Digermulen Peninsula using rare earth elements and Sm–Nd and Rb–Sr isotopic systematics to provide an environmental context and better understand this important transition in Earth’s history. The studied sections comprise a mid-Ediacaran glacial–interglacial cycle, including the Nyborg Formation (ca. 590 Ma) and Mortensnes Formation (related to the ca. 580 Ma-old Gaskiers glaciation), and the Stáhpogieddi Formation (ca. 560–537 Ma), which yields Ediacara-type fossils in the Indreelva Member and contains the Ediacaran–Cambrian boundary interval in the Manndrapselva Member and basal part of the informal Lower Breidvika member (ca. 537–530 Ma). Three sample groups, (1) Nyborg and Mortensnes formations, (2) the lowermost five samples from the Indreelva Member and (3) the remaining samples from the Indreelva as well as from the Manndrapselva and Lower Breidvika members, can be distinguished, belonging to distinct depositional units. All samples have negative εNd(T) values (−6.00 to − 21.04) indicating a dominant input of terrigenous detritus with an old continental crust affinity. Significant shifts in Sm–Nd isotope values are related to changes in the sediment source, i.e. Svecofennian province vs Karelian province vs Svecofennian province plus in addition likely some juvenile (late Neoproterozoic volcanic) material, and probably reflect palaeotectonic reorganisation along the Iapetus-facing margin of Baltica. The combined Rb–Sr isotopic data of all samples yield an errorchron age of about 430 Ma reflecting the resetting of the Rb–Sr whole-rock isotope systems of the mudstones during the Scandian tectono-metamorphic event in the Gaissa Nappe Complex of Finnmark. Preservation of palaeopascichnids coincides with the sedimentation regimes of sample groups 2 and 3 while other Ediacara-type fossils, e.g. Aspidella-type and frondose forms, are limited to the sample group 3. Our results are similar to those of earlier studies from the East European Platform in suggesting oxic seafloor conditions during the late Ediacaran.

Constraining the geothermal parameters of in situ Rb–Sr dating on Proterozoic shales and their subsequent applications

Abstract. Recent developments in tandem laser ablation mass spectrometer technology have demonstrated the capacity for separating parent and daughter isotopes of the same mass online. As a result, beta-decay chronometers can now be applied to the geological archive in situ as opposed to through traditional whole-rock digestions. One novel application of this technique is the in situ Rb–Sr dating of Proterozoic shales that are dominated by authigenic clays such as illite. This method can provide a depositional window for shales by differentiating signatures of early diagenetic processes versus late-stage secondary alteration. However, the hydrothermal sensitivity of the Rb–Sr isotopic system across geological timescales in shale-hosted clay minerals is not well understood. As such, we dated the Mesoproterozoic Velkerri Formation from the Altree 2 well in the Beetaloo Sub-basin (greater McArthur Basin), northern Australia, using this approach. We then constrained the thermal history of these units using common hydrocarbon maturity indicators and modelled effects of contact heating due to the intrusion of the Derim Derim Dolerite. In situ Rb–Sr dating of mature, oil-prone shales in the diagenetic zone from the Velkerri Formation yielded ages of 1448 ± 81, 1434 ± 19, and 1421 ± 139 Ma. These results agree with previous Re–Os dating of the unit and are interpreted as recording the timing of an early diagenetic event soon after deposition. Conversely, overmature, gas-prone shales in the anchizone sourced from deeper within the borehole were dated at 1322 ± 93 and 1336 ± 40 Ma. These ages are younger than the expected depositional window for the Velkerri Formation. Instead, they are consistent with the age of the Derim Derim Dolerite mafic intrusion intersected 800 m below the Velkerri Formation. Thermal modelling suggests that a single intrusion of 75 m thickness would have been capable of producing a significant hydrothermal perturbation radiating from the sill top. The intrusion width proposed by this model is consistent with similar Derim Derim Dolerite sill thicknesses found elsewhere in the McArthur Basin. The extent of the hydrothermal aureole induced by this intrusion coincides with the window in which kerogen from the Velkerri Formation becomes overmature. As a result, the mafic intrusion intersected here is interpreted to have caused kerogen in these shales to enter the gas window, induced fluids that mobilize trace elements, and reset the Rb–Sr chronometer. Consequently, we propose that the Rb–Sr chronometer in shales may be sensitive to temperatures of ca. 120 ∘C in hydrothermal reactions but can withstand temperatures of more than 190 ∘C in thermal systems not dominated by fluids. Importantly, this study demonstrates a framework for the combined use of in situ Rb–Sr dating and kerogen maturation indicators to help reveal the thermochronological history of Proterozoic sedimentary basins. As such, this approach can be a powerful tool for identifying the hydrocarbon potential of source rocks in similar geological settings.

The timing of blueschist-facies metamorphism in the Makrotantalon Unit on Andros Island, Greece: Cretaceous and Eocene high-pressure/low-temperature events?

AbstractThis study corroborates interpretations suggesting that the Makrotantalon Unit on Andros represents a tectonic slice with Pelagonian affinity in the nappe stack of the Cycladic Blueschist Unit. Previously reported Cretaceous 40Ar–39Ar dates of a garnet-glaucophane schist from the Makrotantalon Unit could not be reproduced by Rb–Sr geochronology, but this is not an indication of contamination with excess Ar. Instead, the newly dated samples record disturbance of the Rb–Sr isotope system by partial recrystallization. Subsets of these phengite populations, representing the smaller grain-size fractions, yielded low-precision dates ranging from c. 21 to c. 15 Ma that document deformation-related resetting and recrystallization of a presumably Cretaceous white mica population. Although these Miocene dates cannot be linked with blueschist-facies metamorphism, they provide time constraints on the formation of shear zones that overprinted the original thrust contact during exhumation. The geological relevance of a Cretaceous high-pressure event is confirmed by a Rb–Sr date of c. 121 Ma for an epidote-glaucophane schist collected further away from the tectonic contact. The occurrence of a second blueschist-facies event in the Eocene is verified by Rb–Sr dates of two epidote-glaucophane schists (c. 40 Ma and c. 44 Ma) that can unambiguously be assigned to the Makrotantalon Unit.