Sr Isotopic Signatures Research Articles

The strongly peraluminous A-type granites of the Characato suite (Achala batholith), Sierras Pampeanas, Argentina: Evidence of Devonian-Carboniferous crustal reworking

The largest igneous body in the Sierras Pampeanas (the Achala batholith) is composed by several magmatic intrusions. How many plutons form this batholith and its intrusive history remains unclear. The emplacement of the batholith began at ca. 380 Ma; the Characato suite, in the northern extreme of the body, represents a relatively young intrusive phase in its construction (ca. 360 Ma). This suite, composed mainly of two-mica monzogranites, correspons to a strongly peraluminous A-type magma (A/CNK > 1.1) with fractionated compositions (high Rb/Sr and Rb/Ba). The parental magma corresponds to a high temperature melt generated by biotite dehydration melting, which was then differentiated to form the Characato monzogranites. These monzogranites have crustal Nd and Srisotope signatures (εNdt −6.0 to −6.1 and 87Sr/86Srt 0.7074 to 0.7131) and abundant inherited zircons (ca. 90%). The inherited ages are mainly Early Cambrian, and to a lesser extent Mesoproterozoic, Neoproterozoic and Ordovician, all they recognized in the basement of the Sierras de Córdoba. The Nd-isotope composition, added to the inherited zircon ages of the Characato suite, indicate that these magmas derived from partial melting of a heterogeneous crust composed by the S-type Pampean granites and migmatites, Famatinian granitoids, and probably the low-to medium-grade metamorphic rocks of the Puncoviscan Series. The high variability and positive εHft values of the inherited Cambrian zircons found in the Characato suite could have been transferred from the Neoproterozoic grains of the Puncaviscana Series to the Early Cambrian S-type granites and migmatites during the Pampean orogeny.

Plant Sr Isotope Ratios As Affected by the Sr Isotope Ratio of the Soil and of the External Sr Inputs.

The 87Sr/86Sr ratio of a produce is generally linked with the soil geological features of the growing areas. This study aimed at assessing to which extent the addition of external Sr by agricultural practices, like irrigation and mineral nutrient supply, influences this relationship. In a first experiment, oat plants in two soils reflected the 87Sr/86Sr of the soil. However, this link was significantly altered at increasing levels of external Sr soil supplies. In a second experiment, apple trees transplanted in pots modified their original 87Sr/86Sr, which became progressively closer to the soil Sr isotope ratio. The addition of tap water and fertilizers, with different Sr isotopic signatures, slightly affected plant 87Sr/86Sr. Results confirm the potential of the 87Sr/86Sr ratio as a geographical tracer of agricultural commodities, but whenever the range of 87Sr/86Sr variability among soils from different geographical areas is narrow, the influence of external Sr-sources may smooth over these diversities.

Sr Isotope Signature of Glendonites in the Middle Jurassic of Siberia

Sr Isotope Signature of Glendonites in the Middle Jurassic of Siberia

Geochronology, classification and mantle source characteristics of kimberlites and related rocks from the Rae Craton, Melville Peninsula, Nunavut, Canada

Detailed geochronology along with petrographic, mineralogical and geochemical studies have been conducted on recently found diamond-bearing kimberlitic and related rocks in the Rae Craton at Aviat and Qilalugaq, Melville Peninsula, north-east Canada. Magmatic rocks from the Aviat pipes have geochemical (both bulk rock and isotopic) and mineralogical signatures (e.g., core to rim Al and Ba enrichment in phlogopite) similar to Group I kimberlite. In contrast, Aviat intrusive sheets are similar to ‘micaceous’ Group II kimberlite (orangeite) in their geochemical and mineralogical characteristics (e.g., phlogopite and spinel compositions, highly enriched Sr isotopic signature). Qilalugaq rocks with the least crustal contamination have geochemical and mineralogical signatures [e.g., high SiO2, Al2O3 and H2O; low TiO2 and CO2; less fractionated REE (rare earth elements), presence of primary clinopyroxene, phlogopite and spinel compositions] that are similar to features displayed by olivine lamproites from Argyle, Ellendale and West Greenland. The Naujaat dykes, in the vicinity of Qilalugaq, are highly altered due to extensive silicification and carbonation. However, their bulk rock geochemical signature and phlogopite chemistry are similar to Group I kimberlite. U–Pb perovskite geochronology reveals that Aviat pipes and all rocks from Qilalugaq have an early Cambrian emplacement age (540–530 Ma), with the Aviat sheets being ~30 Ma younger. This volatile-rich potassic ultramafic magmatism probably formed by varying degrees of involvement of asthenospheric and lithospherically derived melts. The spectrum of ages and compositions are similar to equivalent magmatic rocks observed from the nearby north–eastern North America and Western Greenland. The ultimate trigger for this magmatism could be linked to Neoproterozoic continental rifting during the opening of the Iapetus Ocean and breakup of the Rodinia supercontinent.

New constraints on the origin of the Maozu carbonate-hosted epigenetic Zn-Pb deposit in NE Yunnan Province, SW China

Micro-scale isotopic compositions determined by micro-beam in situ analysis techniques are expected to provide new information for the understanding of ore genesis. Here we use the Maozu (∼20 Mt of sulfide ore, grading 7.25 wt% Zn and 4.15 wt% Pb) Zn-Pb deposit in the Upper Yangtze Zn-Pb metallogenic province as a case study, utilizing NanoSIMS in situ S, femtosecond LA-MC-ICPMS in situ Pb and conventional bulk Sr isotopes, as well as field data, aimed to reveal its origin and ore formation process. NanoSIMS in situ δ34S values of sulfide minerals from the Maozu deposit have a wider range (+5.9–+20.7‰) than that of bulk δ34S values (+9.9–+19.9‰). Such S isotope signatures reflect the enrichment of heavy S isotopes in ore-forming fluids, and further indicate the source of S is multiple reservoirs (e.g. marine evaporites, coeval seawater, and metamorphic rocks/fluids). Pb isotopic ratios of galena determined by LA-MC-ICPMS in situ techniques have a narrower range (206Pb/204Pb = 18.20–18.21, 207Pb/204Pb = 15.69–15.71 and 208Pb/204Pb = 38.40–38.43) than that of bulk Pb isotopic ratios (206Pb/204Pb = 18.13–18.38, 207Pb/204Pb = 15.64–15.69 and 208Pb/204Pb = 38.22–38.58). This implies that in situ Pb isotopes can truly reflect the source of Pb, which is due to impurities enclosed by sulfide crystals and pollutants introduced by chemical analysis could significantly affect the quality of the bulk Pb isotopic data. Compared with previously reported Pb isotopic data of potential source rocks (i.e. late Permian Emeishan basalts, Paleozoic ore-bearing sedimentary rocks and Proterozoic basement metamorphic rocks), the in situ Pb isotopic data are significantly different from those of basalts, but are similar to those of both basements and sediments. This means that metal-rich fluids were mainly derived from and/or flowed through basements and sediments. Sphalerite separates have initial Sr isotopic ratios (0.711–0.719) that are distinctly different from those of ore formation age-corrected basalts (87Sr/86Sr200 Ma = 0.704–0.708) and basements (87Sr/86Sr200 Ma = 0.724–0.729), whereas partly overlap with those of age-corrected sediments (87Sr/86Sr200 Ma = 0.707–0.714). Such Sr isotope signatures suggest that hydrothermal fluids were predominantly derived from and/or flowed through basements and sediments with a certain influence from basalts. Hence, the Maozu deposit has complex source rocks that are related to the local geological setting. The mixing of metal-rich fluids (related to basements and sediments, and even basalts) and S-bearing fluids (associated with multiple S reservoirs) plays a key role in the formation of sulfide ores. Therefore, the Maozu deposit, formed during Early Mesozoic (∼196 Ma), is an epigenetic Zn-Pb deposit that hosts in carbonate rocks, occurs along fault-fold structures, and has a mixed source of mineralizing elements and associated fluids.

The Hämmerlein skarn-hosted polymetallic deposit and the Eibenstock granite associated greisen, western Erzgebirge, Germany: two phases of mineralization—two Sn sources

The Hammerlein polymetallic deposit is hosted in skarn, schists, and gneisses that reached their metamorphic peak at ~ 340 Ma during the Variscan orogeny. The deposit is spatially closely associated with one of the most voluminous granites of the Erzgebirge, the Eibenstock granite which intruded the metamorphic units at ~ 320 Ma, and locally also developed greisen mineralization. Cassiterite is the main ore mineral in the Hammerlein skarn and in greisen mineralizations associated with the Eibenstock granite. The age of skarn formation is bracketed by multi-mineral Rb-Sr isochron ages of the gneisses (~ 340 Ma) and the end of ductile deformation (> 330 Ma). The dated calc-silicate minerals of the skarn have elevated Sn contents, which implies that some Sn was present in the system during regional metamorphism, i.e., well before the emplacement of the Eibenstock granite. Tin in the > 330 Ma old skarn silicates possibly was mobilized from the metamorphic wall rocks. Retrogression of the skarn mineral assemblage may have released some Sn that formed cassiterite in an assemblage with chlorite and fluorite. The Sr isotope signatures of fluorite indicate that this late assemblage is not related to cooling of the metamorphic rocks, but to the emplacement of the Eibenstock granite, which introduced additional Sn into the skarn. Thus, mineralization in the Hammerlein deposit includes Sn that was introduced during two different events from different sources.

Modelling strontium isotopes in past biospheres – Assessment of bioavailable 87Sr/86Sr ratios in local archaeological vertebrates based on environmental signatures

87Sr/86Sr isotopic ratios in skeletal remains of archaeological vertebrates are used for provenance analysis since long. However, the definition of the past bioavailable isotopic ratio at the site of recovery is not known beforehand and geological maps can provide no more than gross expectations. Therefore, the assessment of the “local Sr isotopic signature” is still of crucial importance. In this study, we present a tool for the prediction of such local isotopic signatures by creating a concentration weighted mixing model that links lithospheric, biospheric, and atmospheric strontium per site. The major strontium sources and their input into an animal's body were assessed by choosing elemental strontium and its isotopic signature in groundwater, soil, vegetation, and precipitation as components for the mixing model, augmented by literature values. The model was applied to 24 sites located in the alpine transect of the Inn-Eisack-Adige-Brenner passage across the European Alps, a passage used since the Mesolithic. Predicted local bioavailable 87Sr/86Sr ratios were compared with measured values from locally excavated archaeozoological bone samples from three taxa of large and mainly residential vertebrates (cattle, pig, red deer) to verify the models' accuracy. With regard to the fact that the environmental samples predict the past local bioavailable 87Sr/86Sr at a specific site while the vertebrates had different and species-specific home ranges, thereby integrating strontium from a region of primarily unknown size, the model is capable of assigning reasonable expectation values. For 11 sites, up to 100% of the vertebrate isotopic signatures were correctly predicted. Mismatches at the remaining sites are explainable by special environmental factors, and also the fact that some import of animals can never be excluded beforehand. Suggestions for site-specific adjustments of the model are made.

Strontium Isotope Stratigraphy: Principles and State of the Art

The methodical basis, development, and current state of a new method of chronostratigraphic studies, i.e., strontium isotope stratigraphy (SIS), are considered. This method makes it possible to date and correlate geographically distant sedimentary sequences without involving the biostratigraphic and isotope geochronological data. SIS is based on secular variations in 87Sr/86Sr in the paleocean, resulting from the redistribution of the roles of two global strontium flows formed in the mantle and continental reservoirs of the Earth. Isotopic homogeneity of Sr in the paleoceans and in the linked seas leads to the fact that the 87Sr/86Sr ratio in the sea basins is individual for each geological time point and is inherited in marine chemogenic sediments under deposition of dissolved Sr as an isomorphic impurity. Low-Mg calcite and also fragments of fossilized paleontological remains buried in situ are the best minerals that are capable of retaining the Sr isotopic signature of the sedimentation environment. SIS is carried out with geochemical diagnostics of secondary alteration of the studied material and selective dissolution of the samples to produce a carbonate material that adequately reflects isotopic signature of the sedimentary basin. Interregional correlations of the Proterozoic and Cenozoic sea sediments and their relation to the SIS-based stratigraphic scale are given as an example.

Human Mobility in the Final Eneolithic Population of Święte, Jarosław District, South-Eastern Poland: Evidence from Strontium Isotope Data

Abstract Strontium isotope ratios (87Sr/86Sr) were applied to investigate provenance amongst the Final Eneolithic population at Święte (sites 11, 15 and 20) in the Subcarpathian region, south-eastern Poland. The study used 11 human enamel samples collected from the niche graves of the Corded Ware culture. To obtain base-line information on the local Sr isotope composition seven animal enamel samples were also examined. They were found in the adjacent archaeological sites of the Mierzanowice culture at Mirocin and Dobkowice, which have the same environmental and geological background as the sites at Święte. The investigated individuals from Święte display a wide spectrum of Sr isotope signatures, from 0.7094 to 0.7109. Because a comparison of human 87Sr/86Sr values from Święte with Sr animal signatures from Early Bronze Age sites in the area is not unambiguous the local range of 87Sr/86Sr values were based on published data for the Subcarpathian population of the Corded Ware culture. Strontium isotope ratios indicate that only three males with the most radiogenic 87Sr/86Sr values exhibit local signatures. Values below 0.7103 document individuals born outside of the Subcarpathian region. Among these are all women and children, two males and one individual with undetermined sex. The probable homeland of the non-local individuals were areas along the northern and eastern margins of the Carpathian Foredeep in Poland and Ukraine.

Rapid determination of initial 87Sr/86Sr and estimation of the Rb-Sr age of plutonic rocks by LA-ICPMS of variably altered feldspars: An example from the 1.14 Ga Great Abitibi Dyke, Ontario, Canada

Sr isotope analysis of plutonic rocks is an important method for deriving the provenance and age of ancient magmatic episodes, and the petrogenetic processes operating during intrusive activity. We determined the 87Sr/86Sr isotopic compositions of fresh and variably altered feldspars from the 1.14 Ga gabbroic Great Abitibi Dyke, Ontario, Canada, through the use of Laser Ablation Inductively-Coupled Plasma Mass Spectrometry (LA-ICPMS). The data show an alteration trend between fresh, low-Rb plagioclase with 87Sr/86Sr ratios of 0.7045 and high-Rb alkali feldspar with 87Sr/86Sr ratios of 0.7059, which may be used to constrain the 87Sr/86Sr ratio of the mantle source. This trend is incompatible with simple mixing and instead has age significance. As post-intrusive alteration through hydrothermal circulation starts immediately following emplacement, LA-ICPMS analysis allows rapid estimation of initial 87Sr/86Sr ratios and intrusive age, suitable for sample screening and selection for more precise dating. For the Great Abitibi Dyke, the Rb-Sr age estimate of emplacement of 1.10 ± 0.23 Ga (2σ) is concordant with the precise U-Pb emplacement age of the dyke (1140.6 ± 2.0 Ma). The most altered high-Rb alkali feldspars return younger ages, suggesting that post-intrusive alteration lasted several hundred million years. This study highlights the need for microanalysis to differentiate between alteration and magmatic processes on basis of Sr isotopic signatures, and outlines a rapid method to determine initial 87Sr/86Sr ratios and to estimate Rb-Sr ages of plutonic rocks in terranes with long histories of multiple intrusive magmatic episodes.

Strontium isotopes reveal weathering processes in lateritic covers in southern China with implications for paleogeographic reconstructions.

The isotope ratios of Sr are useful tracers for studying parent material sources, weathering processes, and biogeochemical cycling. Mineralogical and geochemical investigations of two lateritic weathering covers, in an area close to the Tropic of Cancer (Guangxi Province, southern China), were undertaken to study the regional weathering processes and Sr isotopic sources. We found that weathering and decomposition of Rb- and Sr-bearing minerals change the Sr isotopic composition in weathering products (lateritic soils). Weathering of illite lowered the 87Sr/86Sr ratio whereas dissolving and leaching of carbonate minerals increased the 87Sr/86Sr ratio. An Fe nodular horizon is widely developed on the top of the weathering covers in the studied area and it differs from the lateritic soil horizon in mineral composition, construction, and elemental concentration. Furthermore, both Fe2O3 and P2O5 (concentrations) are negatively correlated with the 87Sr/86Sr ratios, suggesting fixation of apatite by Fe oxides is a controlling factor of the Sr isotopic composition in the Fe nodular horizon. The 87Sr/86Sr and Nb/Sr ratios imply the contents and proportions of Fe nodules and clay are critical in controlling the changes of Sr isotopic composition in the Fe nodular horizon. The two stages of the weathering process of carbonate rocks are revealed by the87Sr/86Sr versus Nb/Sr diagram. The 87Sr/86Sr and Rb/Sr ratios suggest that Sr isotopes in the weathering covers within the studied area are derived mainly from parent rock weathering and that the contributions from allothogenic Sr isotopes are limited. A comparison of Sr isotopic composition signatures in the weathering covers of the studied area and Guizhou Province provided insight into the Sr isotopic source and paleogeographic evolution of southern China. From the Permian to the Triassic, the continental fragment sources of the South China sedimentary basin changed significantly. In the Permian, Southern China presented the paleogeographic pattern that the north was higher (in elevation) than the south.

Linking Barbados Mineral Dust Aerosols to North African Sources Using Elemental Composition and Radiogenic Sr, Nd, and Pb Isotope Signatures

AbstractLarge quantities of African dust are carried across the Atlantic to the Caribbean Basin and southern United States where it plays an important role in the biogeochemistry of soils and waters and in air quality. Dusts' elemental and isotopic composition was comprehensively characterized in Barbados during the summers of 2013 and 2014, the season of maximum dust transport. Although total suspended insoluble particulate matter (TSIP) mass concentrations varied significantly daily and between the two summers, the abundances (μg element/g TSIP) of 50 elements during “high‐dust days” (HDD) were similar. Aerosols were regularly enriched in Na, Cu, Zn, As, Se, Mo, Cd, Sn, Sb, and W relative to the upper continental crust. Enrichment of these elements, many of which are anthropogenically emitted, was significantly reduced during HDD, attributed to mixing and dilution with desert dust over source regions. Generally, Ti/Al, Si/Al, Ca/Al, Ti/Fe, Si/Fe, and Ca/Fe ratios during HDD differed from their respective values in hypothesized North African source regions. Nd isotope composition was relatively invariant for “low‐dust days” (LDD) and HDD. In contrast, HDD‐aerosols were more radiogenic exhibiting higher 87Sr/86Sr, 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios compared to LDD. Generally, Barbados aerosols' composition ranged within narrow limits and was much more homogeneous than that of hypothesized African source soils. Our results suggest that summertime Barbados aerosols are dominated by a mixture of particles originating from sources in the Sahara‐Sahel regions. The Bodélé Depression, long suspected as a major source, appears to be an insignificant contributor of summertime western Atlantic dust.

Miocene Oceanographic Evolution Based on the Sr and Nd Isotope Record of the Central Mediterranean

AbstractThe Miocene is a key interval in the geodynamic and oceanographic evolution of the Mediterranean marking the transition from a wide open basin to the modern closed basin. We used the Sr and Nd isotope records of two Miocene carbonate successions in the Adriatic to document that the evolution of the Mediterranean Basin controlled its seawater chemistry. During the late Aquitanian (~21 Ma), a time of glaciation and sea level lowstand, increased runoff affected the Sr isotope ratios of Mediterranean waters, whereas during the Burdigalian (20.44–15.97 Ma) volcanism in the circum‐Mediterranean area mainly influenced the Sr isotopic signature. During the Langhian (15.97–13.82 Ma), a time of sea level highstand associated with the Middle Miocene Climatic Optimum, the Nd isotope values indicate that waters exchanged between the Paratethys and the Central Mediterranean. The Central Mediterranean was well connected with the Atlantic Ocean between the Langhian and the early Tortonian (15.97–11.5 Ma), but exchange of water with the Paratethys declined. In the Messinian (6.3 Ma), connections between some marginal Mediterranean basins, for example, the proto‐Adriatic basin, and the Central Mediterranean, became restricted. In this basin, the Sr isotope values fell below the global reference line, while Nd isotope ratios show a strong affinity with the Atlantic Ocean and also indicate freshwater input. We conclude that the Mediterranean Nd isotope signature differs from that in the open oceans and reflects the basin physiography, reflecting a mix of signals derived from the adjacent oceans and local signals.

Petrogenesis of Rabor-Lalehzar magmatic rocks (SE Iran): Constraints from whole rock chemistry and Sr-Nd isotopes

The Urumieh-Dokhtar magmatic arc (UDMA) of Central Iran has been formed during Neotethyan Ocean subduction underneath Eurasia. The Rabor-Lalehzar magmatic complex (RLMC), covers an area ∼1000 km2 in the Kerman magmatic belt (KMB), SE of UDMA. RLMC magmatic rocks include both granitoids and volcanic rocks with calc-alkaline and adakitic signatures but with different ages.Miocene adakitic rocks are characterd by relatively enrichmented in incompatible elements, high (Sr/Y)(N) (>40), and (La/Yb)(N) (>10) ratios with slightly negative Eu anomalies (EuN/Eu*≈ 0.9), depletion in HFSEs, and relatively non-radiogenic Sr isotope signatures (87Sr/86Sr = 0.7048–0.7049). In contrast, the Oligocene granitoids exhibit low Sr/Y (<20) and La/Yb (<9) ratios, negative Eu anomalies (EuN/Eu* ≈ 0.5), and enrichment in HFSEs and radiogenic Sr isotope signatures (87Sr/86Sr = 0.7050–0.7052), showing affinity to the island arc rocks. Eocene volcanic rocks which crusscut the younger granitoid rocks comprise andesites and dacites. Geochemically, lavas show calc-alkaline character without any Eu anomaly (EuN/Eu* ≈ 1.0). Based on the geochemical and isotopic data we propose that melt source for both calc-alkaline and adakitic rocks from the RLMC can be related to the melting of a sub-continental lithospheric mantle (SCLM). Basaltic melts derived from a metasomatized mantle wedge might be emplaced at the mantle-crust boundary and formed the juvenile mafic lower crust. However, some melts fractionated in the shallow magma chambers and continued to rise forming the volcanic intermediate-mafic rocks at the surface. On the other hand, the assimilation and fractional crystallization in the shallow magma chambers of may have been responsible for the development of Oligocene granitoids with calc-alkaline affinity. In the mid-Late Miocene, following the collision between Afro-Arabia and Iranian block the juvenile mafic crust of UDMA underwent thickening and metamorphosed into garnet-amphibolites. Subsequent upwelling of a hot asthenosphere during Miocene was responsible for partial melting of thickened juvenile crust of the SE UDMA (RLM complex). The adakitic melts ascended to the shallow crust to form the adakitic rocks in the KMB.

In situ Sr Isotope Compositions of Plagioclase from a Complete Stratigraphic Profile of the Bushveld Complex, South Africa: Evidence for Extensive Magma Mixing and Percolation

The cumulates of the Bushveld Complex, which form the largest layered intrusion on Earth, are known to have crystallized from several isotopically distinct magma pulses. Here, we present in situ Sr isotope compositions combined with the corresponding mineral chemistry of plagioclase from all lithological zones, covering > 6 km of stratigraphy, to constrain the petrogenesis of the complex. The in situ data coupled with high-resolution elemental maps of individual plagioclase grains reveal complex zonation patterns with respect to mineral chemistry and Sr isotope composition. This suggests that interstitial plagioclase in the Bushveld Complex crystallized from multiple, isotopically distinct influxes of melt percolating through a mafic cumulate framework and displacing the resident melt. Similarly, cumulus plagioclase grains are the result of continual ingress of a distinct magma, which picked up previously formed plagioclase crystals. Sr isotope compositions across the layered sequence seem to be largely decoupled from differentiation indices, such as Mg#, anorthite content or trace element ratios. As these observations cannot be explained by bulk assimilation, we propose that the elevated Sr isotopic signature of the Bushveld cumulates may have resulted from the interaction of the parental magma with a fluid derived from the up to 2 km thick dolomitic footwall, which caused a major shift in Sr isotope composition without significantly affecting the degree of differentiation or trace element signature. The decarbonation and/or assimilation of dolomite during the intrusion of the Bushveld Complex may be of major importance, not only for the petrogenesis but also for the emplacement of the layered intrusion, because devolatilization is directly linked to space creation owing to volume loss, thus producing a lopolith.

Application of strontium isotope analysis to provenance studies of Early Bronze Age North-Mesopotamian Metallic Ware

Sr isotopic analysis was carried out on Early Bronze Age (c. 2800–2200BCE) North-Mesopotamian Metallic Ware and clay samples collected from south-eastern Anatolia and north-eastern Syria with a view to determining the provenance of this characteristic ceramic type, in particular of its non-calcareous variant. The non-calcareous and calcareous variants of North-Mesopotamian Metallic Ware, which have been defined in previous archaeometric studies, show a clear distinction in their Sr isotopic signatures. The non-calcareous group is characterised by high 87Sr/86Sr ratios, whereas the calcareous variant has much lower values. The Sr isotopic signature of the non-calcareous group shows similarities with clay samples from the Pütürge Massif area in south-east Anatolia. Combining the results of the present study with previous investigations, it is thought that the raw material used for the production of non-calcareous North-Mesopotamian Metallic Ware could have been originated from the southern part of the Pütürge Massif area. Furthermore, this study proves that Sr isotope analysis is a useful tool for the characterisation and identification of archaeological ceramic provenance.

In situ Pb and bulk Sr isotope analysis of the Yinchanggou Pb-Zn deposit in Sichuan Province (SW China): Constraints on the origin and evolution of hydrothermal fluids

The Yinchanggou Pb-Zn deposit, located in southwestern Sichuan Province, western Yangtze Block, is stratigraphically controlled by late Ediacaran Dengying Formation and contains >0.3 Mt of metal reserves with 11wt% Pb+Zn. A principal feature is that this deposit is structurally controlled by normal faults, whereas other typical deposits nearby (e.g. Maozu) are controlled by reverse faults. The origin of the Yinchanggou deposit is still controversial. Ore genetic models, based on conventional whole-rock isotope tracers, favor either sedimentary basin brine, magmatic water or metamorphic fluid sources. Here we use in situ Pb and bulk Sr isotope features of sulfide minerals to constrain the origin and evolution of hydrothermal fluids. The Pb isotope compositions of galena determined by femtosecond LA-MC-ICPMS are as follows: 206Pb/204Pb=18.17–18.24, 207Pb/204Pb=15.69–15.71, 208Pb/204Pb=38.51–38.63. These in situ Pb isotope data overlap with bulk-chemistry Pb isotope compositions of sulfide minerals (206Pb/204Pb=18.11–18.40, 207Pb/204Pb=15.66–15.76, 208Pb/204Pb=38.25–38.88), and both sets of data plotting above the Pb evolution curve of average upper continental crust. Such Pb isotope signatures suggest an upper crustal source of Pb. In addition, the coarse-grained galena in massive ore collected from the deep part has higher 206Pb/204Pb ratios (18.18–18.24) than the fine-grained galena in stockwork ore sampled from the shallow part (206Pb/204Pb=18.17–18.19), whereas the latter has higher 208Pb/204Pb ratios (38.59–38.63) than the former (208Pb/204Pb=38.51–38.59). However, both types of galena have the same 207Pb/204Pb ratios (15.69–15.71). This implies two independent Pb sources, and the metal Pb derived from the basement metamorphic rocks was dominant during the early phase of ore formation in the deep part, whereas the ore-hosting sedimentary rocks supplied the majority of metal Pb at the late phase in the shallow part. In addition, sphalerite separated from different levels has initial 87Sr/86Sr ratios ranging from 0.7101 to 0.7130, which are higher than the ore formation age-corrected 87Sr/86Sr ratios of country sedimentary rocks (87Sr/86Sr200Ma=0.7083–0.7096), but are significantly lower than those of the ore formation age-corrected basement rocks (87Sr/86Sr200Ma=0.7243–0.7288). Again, such Sr isotope signatures suggest that the above two Pb sources were involved in ore formation. Hence, the gradually mixing process of mineralizing elements and associated fluids plays a key role in the precipitation of sulfide minerals at the Yinchanggou ore district. Integrating all the evidence, we interpret the Yinchanggou deposit asa strata-bound, normal fault-controlled epigenetic deposit that formed during the late Indosinian. We also propose that the massive ore is formed earlier than the stockwork ore, and the temporal-spatial variations of Pb and Sr isotopes suggest a certain potential of ore prospecting in the deep mining area.

Weathering fluxes and sediment provenance on the SW Scottish shelf during the last deglaciation

The reconstruction of past ice sheet dynamics can inform on long-term ice stream activity, and in turn provide constraints on the response of modern ice sheets to climate change. The Hebrides Ice Stream (HIS) flowed across part of the western Scottish shelf to the shelf-break during the last glacial cycle. To investigate the deglacial dynamics of the HIS following the Last Glacial Maximum (LGM), lead (Pb) isotope records were extracted from the FeMn oxyhydroxide and detrital fractions of recovered laminated glacimarine mud sequences to monitor the changing activity of HIS during its retreat. These provide, respectively, relative timing of glacially weathered inputs to the marine environment and some source information on the eroded sediments. The FeMn oxyhydroxide fraction is dominated by pre-formed particles and shows a marked decrease from radiogenic at ~21cal ka to less radiogenic Pb isotope compositions towards 15.4–13ka. This decrease represents a reduction in the flux of subglacially-derived radiogenic Pb to the continental shelf, and it is interpreted as the result of the break-up of the ice-stream in western Scotland around that time. The Pb, Sr and Nd isotopic signatures of the detrital fraction indicate a preponderance of fine sediments originated from the NW Highlands throughout the period studied (~21 to 15cal ka BP), most likely dictated by the orientation of tidal and oceanic current directions and sediment delivery. Both fractions show inversion of the 208Pb/204Pb ratio relative to the other Pb isotope ratios. This is observed only in one core site in the detrital fraction, and extended to all cores in the FeMn oxyhydroxide fraction. This behaviour highlights the influence of ocean currents in restricting the detrital but encouraging dispersal of the FeMn oxyhydroxide signal. Periodic increased contributions from a high Th/U source, potentially the neighbouring Archaean amphibolitic Lewisian basement in the Outer Hebrides, are proposed as the source of these 208Pb/204Pb inversions. This study demonstrates how geochemical investigation on continental shelves can be used to constrain the activity and flow sources of palaeo-ice streams, and the utility of combining detrital and FeMn oxyhydroxides to determine the combined influence of the continental sources of material and their dispersal in the marine environment.

Suspected limited mobility of a Middle Pleistocene woman from Southern Italy: strontium isotopes of a human deciduous tooth

We present the Sr isotopic composition of enamel of the most ancient deciduous tooth ever discovered in Italy to assess human mobility in Middle Pleistocene. Reconstructing ancient mobility is crucial for understanding human strategy at exploiting temporally and spatially patchy resources, with most studies focusing on indirect evidences, ultimately affecting our interpretation on hominin territoriality and energetic costs invested by hominin groups. Here, we use the high spatial resolution and micro-destructivity options offered by the Laser Ablation Multi-Collector Inductively Coupled Plasma Mass Spectrometry technique, to determine the 87Sr/ 86Sr intra-tooth variability of a human deciduous incisor from the Middle Pleistocene layers of the Isernia La Pineta site (Italy). We compared these data with the Sr isotopic signature of local micro-mammals, the broadest home-range of the macro-mammals and with modern plant samples. Our study reveals that while macro-mammals have possibly migrated through the landscape for up to 50 km, the pregnant woman from Isernia was probably local, given that the isotopic ratio of the enamel falls within the local range and is comparable with the signature of the local plants in a radius of 10 km. This is the first case study of Sr isotopic composition determination in such ancient deciduous tooth.

Sr-isotope analysis of speleothems by LA-MC-ICP-MS: High temporal resolution and fast data acquisition

Speleothems are well established climate archives. A wide array of geochemical proxies, including stable isotopes and trace elements are present within speleothems to reconstruct past climate variability. However, each proxy is influenced by multiple factors, often hampering robust interpretation. Sr isotope ratios (87Sr/86Sr) can provide useful information about water residence time and water mixing in the host rock, as they are not fractionated during calcite precipitation. Laser ablation multi-collector-inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) has rarely been used for determination of Sr isotope signatures in speleothems, as speleothems often do not possess appropriately high concentrations of Sr to facilitate this analysis. Yet the advantages of this approach include rapid data acquisition, higher spatial resolution, larger sample throughput and the absence of chemical treatment prior to analysis. We present LA-MC-ICP-MS Sr isotope data from two speleothems from Morocco (Grotte de Piste) and India (Mawmluh Cave), and we compare linescan and spot analysis ablation techniques along speleothem growth axes. The analytical uncertainty of our LA-MC-ICP-MS Sr data is comparable to studies conducted on other carbonate materials. The results of both ablation techniques are reproducible within analytical error, implying that this technique yields robust results when applied to speleothems. In addition, several comparative measurements of different carbonate reference materials (i.e. MACS-3, JCt-1, JCp-1), including tests with standard bracketing and comparison of the 87Sr/86Sr ratios with a nanosecond laser ablation system and a state-of-the-art femtosecond laser ablation system, highlight the robustness of the method.