87Rb-87Sr constraints on the genesis and evolution of the Cantal continental volcanic system (France)

We have investigated 24 whole rocks and mineral separates of five different rock types from the Cantal shield volcano in France, applying high-precision Rb-Sr techniques. The chemical and isotopic systematics suggest the distinction of two series throughout the different rock classes, one practically uncontaminated, the other seriously influenced by wall rock assimilation. The first group comprises basalts and intermediate rocks with⁸⁷Sr/⁸⁶Sr= 0.70340–0.70382. The second group in addition includes rhyolites and the corresponding⁸⁷Sr/⁸⁶Sr ratios vary between 0.70421 and 0.71270. The data of mineral separates support the hybridization hypothesis and possibly suggest an original⁸⁷Sr/⁸⁶Sr ratio of 0.7028 for the magma source region. Moreover they provide internal isochron ages which place a period of extensive volcanic activity at 8.1–8.8 m.y. ago in accord with K-Ar ages of volcanic rocks from the center of the Cantal volcano.     

Marine87Sr/86Sr ratios from the Jurassic to Pleistocene: evidence from groundwaters in Israel

Oceanic⁸⁷Sr/⁸⁶Sr ratios during Jurassic to Pleistocene have been determined by analysing fresh waters from marine limestone and dolomite aquifers. The results are in good agreement with published data from well preserved fossil material. The⁸⁷Sr/⁸⁶Sr ratios obtained are 0.7070 for Lower to Middle Jurassic, 0.7075 for Late Cretaceous, 0.7080 for Lower to Middle Eocene and 0.7087 for Pleistocene aquifer waters. The value of⁸⁷Sr/⁸⁶Sr for the Eimer and Amend isotopic standard was 0.7082.     

87Sr/86Sr ratios in hydrothermal waters and deposits from the East Pacific Rise at 21°N

⁸⁷Sr/⁸⁶Sr ratios of three hydrothermal waters collected on the East Pacific Rise at 21°N define a mixing line between seawater and a hydrothermal end-member at 0.7030 which is derived by seawater-basalt interaction at ca. 350°C and water/rock ratio of about 1.5. Sr concentrations are not affected in the process while Mg uptake from seawater is almost complete. Up to2/3 of this hydrothermal component is involved in anhydrite precipitation while the Sr isotopic ratio in sulfides (chalcopyrite + sphalerite) cannot be distinguished from that of sulfate. It is estimated that ca. 1 × 10¹⁰ moles of strontium are yearly cycled in the hydrothermal systems of mid-oceanic ridges, thereby affecting the⁸⁷Sr/⁸⁶Sr budget of seawater. Mass balance between river runoff, limestone precipitation and ridge basalt alteration suggests that the⁸⁷Sr/⁸⁶Sr ratios of the river runoff are in the range 0.7097–0.7113, and are largely dominated by limestone alteration.     

The effects of assimilation of country rocks by magmas on 18O/16O and 87Sr/86Sr systematics in igneous rocks

Examples of positive correlations between initial ⁸⁷Sr/⁸⁶Sr and δ¹⁸O have now been shown to be very common in igneous rock series. These data in general require some type of mixing of mantle-derived igneous rocks with high-¹⁸O, high-⁸⁷Sr crustal metamorphic rocks that once resided on or near the Earth's surface, such as sedimentary rocks or hydrothermally altered volcanic rocks. Mixing that involves assimilation of country rocks by magmas, however, is not a simple two-end-member process; heat balance requires appreciable crystallization of cumulates. In such cases, the isotopic compositions may strongly reflect this open-system behavior and indicate the process of assimilation, whereas the major element chemical compositions of the contaminated magmas will be largely controlled by crystal-melt equilibria and crystallization paths fixed by multicomponent cotectics. A variety of oxygen and strontium isotope “mixing” curves were therefore calculated for this process of combined assimilation-fractional crystallization. The positions and characteristics of the resultant curves on δ¹⁸O-⁸⁷Sr/⁸⁶Sr diagrams markedly diverge from simple two end-member mixing relationships. Based on the above, model calculations can be crudely fitted to two igneous rock suites (Adamello and Roccamonfina in Italy), but the shapes of the calculated curves appear to rule out magmatic assimilation as an explanation for most δ¹⁸O-⁸⁷Sr/⁸⁶Sr correlations discovered so far, including all of those involving calc-alkaline granitic batholiths and andesitic volcanic rocks. The isotopic relationships in such magma types must be inherited from their source regions, presumably reflecting patterns that existed in the parent rocks (or magmas) prior to or during melting.     

87Rb-87Sr chronology of enstatite meteorites

A⁸⁷Rb-⁸⁷Sr analysis of some enstatite meteorites has been made. Whole rocks plot on an isochron of age 4.508 ± 0.037b.y. and strontium initial ratio 0.69880 ± 0.00044 (2σ errors; λ⁸⁷Rb= 1.42 × 10^?11yr^?1) . If the Norton County results are joined, we get an age of 4.516 ± 0.029b.y. and initial ratio of 0.69874 ± 0.00022. This result is indistinguishable from the whole rock isochron for H chondrites. It is interpreted as the age of condensation from the solar nebula. The identity of the⁸⁷Sr/⁸⁶Sr initial ratio with the ones for Allende white inclusions shows that this ratio was homogeneous in the solar nebula, and that the Rb-Sr fractionations observed between the different chondrite groups appeared only shortly before or during condensation accretion.Internal studies of the type-I enstatite chondrites Abee and Indarch and the intermediate-type Saint Mark's and Saint Sauveur have been done.Abee data scatter in the⁸⁷Rb-⁸⁷Sr diagram. For Indarch, Saint Mark's and Saint Sauveur, we obtained well-defined straight lines of “age” (T) and “initial ratio” (I): Indarch,T = 4.393 ± 0.043b.y.I = 0.7005 ± 0.0009; Saint Mark's,T = 4.335 ± 0.050b.y.I = 0.69979 ± 0.00022; Saint Sauveur,T = 4.457 ± 0.047b.y.I = 0.6993 ± 0.0014. Our result on Indarch agrees with the former result of Gopalan and Wetherill [5].A careful examination of the data shows that these straight lines are neither due to leaching effects by heavy liquids, nor result from terrestrial weathering. The “isochrons” for Indarch and Saint Sauveur can be mixing lines between enstatite and feldspar. The results are interpreted in terms of cosmochemical secondary effects: type-I and intermediate-type enstatite chondrites have been shocked 60–200 m.y. after their formation. This agrees with the idea of an early generalized bombardment of the inner solar system; this also indicates that type-I enstatite chondrites were rather situated in the outershells of their parent body and might be at the origin of the scatter of I-Xe ages of enstatite meteorites.Whole rock and enstatite from Bishopville, Cumberland Falls and Mayo Belwa have also been analysed. In these three aubrites, the⁸⁷Rb-⁸⁷Sr system is perturbed. Our Bishopsville sample might not be fresh and this makes the significance of our results uncertain. Cumberland Falls and Mayo Belwa probably suffered relatively recent shocks and open-system redistribution of Rb and Sr.     

143Nd/144Nd,87Sr/86Sr and trace element constraints on the petrogenesis of Aleutian island arc magmas

¹⁴³Nd/¹⁴⁴Nd,⁸⁷Sr/⁸⁶Sr and trace element results are reported for volcanic and plutonic rocks of the Aleutian island arc. The Nd and Sr isotopic compositions plot within the mantle array with ε_Nd values of from 6.5 to 9.1 and⁸⁷Sr/⁸⁶Sr ratios of from 0.70289 to 0.70342. Basalts have mildly enriched light REE abundances but essentially unfractionated heavy REE abundances, while andesites exhibit a greater degree of light to heavy REE fractionation. Both the basalts and andesites have significant large ion lithophile element to light rare earth element (LILE/LREE) enrichments. Variations in the isotopic compositions of Nd and Sr are not related to the spatial distribution of volcanoes in the arc, nor are they related to temporal differences. ε_Nd and⁸⁷Sr/⁸⁶Sr do not correlate with major element compositions but do, however, correlate with certain LILE/LREE ratios (e.g. Ba_N/La_N). Plutonic rocks have isotropic and trace element characteristics identical to some of the volcanic rocks. Rocks that make up the tholeiitic, calc-alkaline and alkaline series in the Aleutians do not come from isotopically distinct sources, but do exhibit some differing LILE characteristics.Given these elemental and isotopic constraints it is shown that the Aleutian arc magmas could not have been derived directly from homogeneous MORB-type mantle, or fresh or altered MORB subducted beneath the arc. Mixtures of partially altered MORB with deep-sea sediment can in principle account for the isotopic characteristics and most of the observed LILE/LREE enrichments. However, some samples have exceedingly high LILE/LREE enrichments which cannot be accounted for by sediment contamination alone. For these samples a more complex scenario is considered whereby dehydration and partial melting of the subducted slab, containing less than 8% sediment, produces a LILE-enriched (relative to REE) metasomatic fluid which interacts with the overlying depleted mantle wedge. The isotopic and LILE characteristics of the mantle are extremely sensitive to metasomatism by small percentages of added fluid, whereas major elements are not substantially effected, Major element compositions of Aleutian magmas are dominantly controlled by the partial melting of this mantle and subsequent crystal fractionation; whereas isotopic and LILE characteristics are determined by localized mantle heterogeneities.     

87Rb87Sr systematics of a geothermal water-rock association in the Massif Central,France

Rb and Sr concentrations and Sr isotopic composition have been measured in thermo-mineral waters from the Massif Central in France. Rocks and mineral fractions which are thought to be important Sr contributors were also analyzed. The results suggest the waters to be mixtures of two or three components from different reservoirs, which can be associated with possible source rock types like granite and syenodiorite occurring in the region. The strontium isotopic ratios found in the separated minerals of the syenodiorite stratum indicate no chemical fractionation during the water-rock interaction. A RbSr internal isochron age of(265 ± 10) × 10⁶yr is inferred for the Roche d'Enval syenodiorite.     

Oxygen isotopes and the origin of high-87Sr/86Sr andesites

Andesites from the Peruvian Andes and the Banda arc of Indonesia are characterized by unusually high and variable ⁸⁷Sr/⁸⁶Sr ratios. The Banda arc samples, including two cordierite-bearing lavas from Ambon, show a clear positive correlation between ⁸⁷Sr/⁸⁶Sr and δ¹⁸O. The andesitic rocks have δ¹⁸O values that range from 5.6 to 9.2‰. Over that range in δ¹⁸O, ⁸⁷Sr/⁸⁶Sr increases from 0.7044 to 0.7095. The cordierite-bearing lavas have δ¹⁸O values of approximately 15‰ and ⁸⁷Sr/⁸⁶Sr ratios of approximately 0.717. The similarity between δ¹⁸O values and ⁸⁷Sr/⁸⁶Sr ratios in total rocks and separated plagioclase phenocrysts of the Banda arc samples indicates that the measured isotope ratios are primary and have not been affected by secondary, low-temperature post-eruptive alteration. The observed variation between O and Sr isotopic ratios can be modeled by two-component mixing in which one component is of mantle isotopic composition. As the crust beneath the Banda arc is probably oceanic, contamination of the manle component may have resulted from the subduction of either continentally-derived sediments or continental crust. Mixing calculations indicate that the contaminant could have an isotopic composition similar to that observed in the cordierite-bearing lavas.The Andean samples, despite petrographic evidence of freshness, exhibit whole-rock δ¹⁸O values significantly higher than those of corresponding plagioclase phenocryst separates, indicating extensive low-temperature post-eruptive alteration. The plagioclase mineral separates show a range of δ¹⁸O values between 6.9 and 7.9‰. The ⁸⁷Sr/⁸⁶Sr ratios of these same samples are, in most instances, not significantly different from those measured for the whole rock, thus signifying that the phenocrysts and groundmass were in isotopic equilibrium at the time of eruption. Unlike the lavas of the Banda arc, the Andean lavas show no strong positive correlation between ⁸⁷Sr/⁸⁶Sr ratios and δ¹⁸O values, but instead lower ⁸⁷Sr/⁸⁶Sr ratios appear to be associated with higher δ¹⁸O values. The δ¹⁸O and ⁸⁷Sr/⁸⁶Sr values of the Peruvian samples are both slightly higher than those of “normal” island arc volcanics.The small proportions of contaminant implied by the O isotope results seem to preclude continental crustal contamination as a primary cause of high ⁸⁷Sr/⁸⁶Sr ratios. The most plausible process that can explain both O and Sr isotope results is one in which sediments of continental origin are partially melted in the subduction zone. These melts rise into overlying mantle material and subsequently participate in the formation of calc-alkaline magmas.If the involvement of a sialic component in the genesis of andesitic magma occurs in the subduction zone, melting of that sialic material signifies temperatures of at least 750–800°C at the top of the subducted lithospheric slab at depths of approximately 150 km. The fact that contamination has apparently occurred in the Banda arc samples without producing any simple widespread correlations between Sr and O isotopic compositions on the one hand and major or trace element abundances on the other, shows that isotopic correlations, possibly including pseudo-isochrons, can be produced by mixing without producing trace element mixing correlations. Because O versus Sr isotope correlations are little affected by processes of partial melting of differentiation, they provide a direct means of testing whether Sr isotopic variations in volcanic rocks are of mantle origin or are due instead to mixing with sialic material.     

87Rb/87Sr study of diogenites

The five diogenites, Johnstown, Roda, Ellemeet, Shalka and Tatahouine, give scattered data in the⁸⁷Rb/⁸⁶Sr,⁸⁷Sr/⁸⁶Sr diagram. This can result from a disturbance which occurred later than 4.45 Ga ago. However, it is shown that if samples of sufficient size were analyzed, there meteorites could plot on the eucrite isochron and are thereby in agreement with a genetic relation between eucrites, howardites and diogenites. The age of eucrite differentiation from diogenites has been computed using data from the two families yielding an age of 4.47±0.1Ga(2σ) (λ=1.42×10^?11a^?1), the initial⁸⁷Sr/⁸⁶Sr ratio being BABI.     

Sr isotope diversity of hot spring and volcanic lake waters from Zao volcano,Japan

The ratio of ⁸⁷Sr/⁸⁶Sr was measured from different water samples of thermal/mineral (hot spring as well as crater lake) and meteoric origins, in order to specify the location and to verify the detailed model of a volcano-hydrothermal system beneath Zao volcano. The ratio showed a trimodal distribution for the case of thermal/mineral water: 0.7052–0.7053 (Type A, Zao hot spring), 0.7039–0.7043 (Type B, Okama crater lake and Shin-funkiko hot spring), and 0.7070–0.7073 (Type C, Gaga, Aone, and Togatta hot springs), respectively. However, in comparison, the ratio was found to be higher for meteoric waters (0.7077–0.7079). The water from the central volcanic edifice (Type B) was found to be similar to that of nearby volcanic rocks in their Sr isotopic ratio. This indicates that the Sr in water was derived from shallow volcanic rocks. The ⁸⁷Sr/⁸⁶Sr ratio for water from the Zao hot spring (Type A) was intermediate between those of the pre-Tertiary granitic and the Quaternary volcanic rocks, thus suggesting that the water had reacted with both volcanic and granitic rocks. The location of the vapor–liquid separation was determined as the boundary of the pre-Tertiary granitic and the Quaternary volcanic rocks by comparing the results of this strontium isotopic study with those of Kiyosu and Kurahashi [Kiyosu, Y., Kurahashi, M., 1984. Isotopic geochemistry of acid thermal waters and volcanic gases from Zao volcano in Japan. J. Volcanol. Geotherm. Res. 21, 313–331.].     

87Sr/86Sr ratios for basalt from Loihi Seamount,Hawaii

⁸⁷Sr/⁸⁶Sr ratios of 15 samples of basalt dredged from Loihi Seamount range from 0.70334 to 0.70368. The basalt types range from tholeiite to basanite in composition and can be divided into six groups on the basis of abundances of K₂O, Na₂O, Rb and Sr and ⁸⁷Sr/⁸⁶Sr ratio. The isotopic data require that the various basalt types be derived from source regions differing in Sr isotopic composition. The Loihi basalts may be produced by mixing of isotopically distinct sources, but the tholeiites and alkalic basalts from Loihi do not show a well-developed inverse trend between Rb/Sr and ⁸⁷Sr/⁸⁶Sr that is characteristic of the later stages of Hawaiian volcanoes such as Haleakala and Koolau.     

87Rb87Sr dating of LL chondrites

⁸⁷Rb⁸⁷Sr analyses of LL chondrites have been made in 10 whole rock meteorites, chondrules from Chainpur (LL3) and Soko Banja (LL4), density separates and chondrules from Guidder (LL5) and density separates from Jelica (LL6) and Ensisheim (LL6). Whole rocks define an isochron of age 4.486±0.020 Ga (λ⁸⁷Rb=1.42×10^?11a^?1) and initial ratio (⁸⁷Sr/⁸⁶Sr)_I=0.69887±0.00012. This is in agreement with the results for H- and E-type chondrites. Analyses for chondrules from Soko Banja yield a very good isochron of age 4.452±0.020 Ga and strontium initial ratio 0.69954±0.00024, and give an interval for metamorphism of (37±10)×10⁶ a. A more poorly defined isochron is obtained for Jelica; the age is 4.423±0.041 Ga and the strontium initial ratio 0.69959±0.00029, indicating an interval for metamorphism of (70±60)×10⁶ a. No isochron could be obtained for Chainpur. This could be due to terrestrial alteration or to a late isotopic disturbance of the meteorite. The⁸⁷Rb-⁸⁷Sr system is also disturbed in Guidder and Ensisheim, probably as a consequence of shock. These results are discussed in comparison with our former studies, and in relation with thermal metamorphism in the LL chondrite parent body(ies).     

87Rb87Sr age of soils and rock from Mare Crisium Luna 24

The soil and one gabbroic fragment from Mare Crisium, brought back by the Luna-24 mission, have been measured through the ⁸⁷Rb/⁸⁷Sr method. The soil is one of the least radiogenic from the moon, comparable with Luna-16 soils. The gabbroic rock, which has a very low Rb/Sr ratio, gives an internal isochron age of 3.74 ± 0.58 Ga and an initial Sr ratio of 0.699085 ± 0.000070.     

87Rb–87Sr history of the Norton County enstatite achondrite

⁸⁷Rb⁸⁷Sr analysis of the Norton County achondrite has been achieved with special attention to the rubidium analysis. Enstatite crystals and polycrystalline material give an “age” of 4.48 ± 0.04 × 10⁹ years and an initial ratio ⁸⁷Sr/⁸⁶Sr_I= 0.7005 ± 0.0004 (λ = 1.39 × 10^?11yr^?1, maximum errors). The feldspar component of the meteorite contains about 70% of the strontium and 30% of the rubidium of the whole sample, and does not lie on the isochron. Its model age relative to the strontium initial ratio of Allende is 4.6 × 10⁹ years. The data are consistent with a complex history dealing with an incomplete isotopic reequilibration of the meteorite, 120 m.y. after its formation at 4.6 × 10⁹ years, with an initial ratio similar to that of Allende.     

“Mantle” Rb/Sr and 87Sr/86Sr ratios for clinopyroxenes from Norwegian garnet peridotites and pyroxenites

Clinopyroxenes separated from garnetiferous ultramafic rocks in the core zone of the Norwegian Caledonides have rubidium concentrations of 0.008 to 0.064 ppm, strontium concentrations of 23.5 to 421 ppm, and ⁸⁷Sr/⁸⁶Sr ratios of 0.7011 to 0.7029. The very low Rb/Sr ratios of the clinopyroxenes (less than 0.0004) suggest that their ⁸⁷Sr/⁸⁶Sr values have not varied significantly over geologic time and may approximate the initial ⁸⁷Sr/⁸⁶Sr of the eclogite-facies ultramafic mineral assemblages at their time of formation. The ultramafic rocks occur in a basement complex that yields Rb-Sr whole-rock and U-Pb zircon ages of about 1800 m.y. Garnetiferous ultramafic rocks are apparently lacking in younger (Sveconorwegian or Caledonian) sialic sequences, raising the possibility that the eclogite-facies metamorphism may have occurred at least 1800 m.y. ago. The Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios of the clinopyroxenes are as predicted for the ancient upper mantle under most evolutionary models. However, the data do not preclude the possibility that the eclogite-facies metamorphism occurred in the crust. The garnetiferous ultramafic rocks are generally enclosed by large volumes of dunite which could have shielded the eclogite-facies assemblages from contamination by fluids from the country rock during metamorphism.     

Strontium isotope identification of water mixing and recharge sources in a river system (Oder River,central Europe): A quantitative approach

This study uses Sr isotope composition (⁸⁷Sr/⁸⁶Sr) and Sr content of waters of the Oder, one of the largest rivers in central Europe, to fingerprint natural and anthropogenic contributions to its Sr budget and to evaluate water mixing processes in its hydrological system. It also demonstrates a simple method of quantifying natural and anthropogenic Sr inputs in the watershed. The method has potential for environmental and archaeological research because past Sr geochemistry of river water can easily be reconstructed. For the first time, a catchment‐scale impact of anthropogenic sources on the Sr budget of a middle‐size river is shown in a quantitative way. The water of the Oder is characterized by a relatively uniform Sr isotope composition, from 0.7100 to 0.7108, contrasting with strong variations in Sr concentration, from 0.25 to 1.27 mg/L. There is a general seasonal trend in variability, with waters becoming more radiogenic and dilute with respect to the Sr in the spring time. This Sr systematics differs significantly from the Sr budgets of the majority of the Oder tributaries that exhibit more radiogenic composition and systematically lower Sr concentrations. A mixing scenario in the Oder involves Sr contribution from four principal water sources: (a) shallow ground waters with Sr derived from near‐surface weathering of silicates, (b) moderately radiogenic mine waters from the Upper Silesian Coal Basin, (c) unradiogenic mine waters from the Permian sequence of the copper district, and (d) unradiogenic ground waters from shallow‐seated Palaeogene, Neogene, and Mesozoic aquifers. The Sr budget of the Oder is primarily controlled by inputs of dissolved Sr from anthropogenic sources, which overprint the natural background, controlled by geology. Thus, about 47.5% of Sr originates from agriculture, industrial, and municipal additions, 31.5% from mine water inputs, and only 21% from natural sources, that is, rock weathering and atmospheric precipitation. Reconstruction of the past Sr chemistry of the Oder reveals that its present‐day Sr isotope composition is temporary and significantly different from that of the preindustrial times.     

Temporal variations in Sr and 87Sr/86Sr of the Ganga headwaters: estimates of dissolved Sr flux to the mainstream

The headwaters of the Ganga (the Alaknanda, Bhagirathi and the Ganga) were analysed for their dissolved major ions, Sr and ⁸⁷Sr/⁸⁶Sr on a biweekly to monthly basis over a period of one year to determine their temporal variations and the factors contributing to them. The concentrations of major ions and Sr show significant seasonal variation with lower values during monsoon period in all the three rivers. A similar trend is also observed for ⁸⁷Sr/⁸⁶Sr and Na*/Ca (Na* = Na_r? Cl_r) suggesting relatively lower contribution of Sr and Na from silicates (which are more radiogenic in Sr) during monsoon. Budget calculations show that silicate derived dissolved Sr (Sr_s) in the river Ganga, Alaknanda and the Bhagirathi varied from 10 ± 4 to 27 ± 11, 7 ± 3 to 30 ± 12, 16 ± 6 to 57 ± 23% of measured Sr respectively with lower values during monsoon. The relative decrease in silicate erosion compared to carbonate during monsoon can result from several factors, these include higher dissolution kinetics of the carbonates, lower water–rock interaction time and availability of larger area for weathering. The annual discharge weighted Sr flux derived from the time series data is higher by ～20% from that based on peak flow Sr, and lower by ～40% compared to that derived from lean flow Sr concentration. The area‐normalized annual flux of dissolved Sr from the Ganga at Rishikesh is about five times its flux at Rajshahi (Bangladesh) and a few other major global rivers, such as the Amazon, indicating higher erosion rate over the Himalaya. Copyright © 2010 John Wiley & Sons, Ltd.     

87Rb87Sr chronology of H chondrites: Constraint and speculations on the early evolution of their parent body

A precise⁸⁷Rb-⁸⁷Sr whole-rock isochron for H chondrites and an internal isochron for Tieschitz (H3) have been determined. The age and⁸⁷Sr/⁸⁶Sr initial ratio of the whole rocks are4.52 ± 0.05 b.y. and0.69876 ± 0.00040(λ(⁸⁷Rb) = 1.42 × 10^?11yr^?1). For Tieschitz, whereas handpicked separates plot on a well-defined line, heavy liquid separates scatter in the⁸⁷Rb/⁸⁶Sr vs.⁸⁷Sr/⁸⁶Sr diagram. Leaching experiments by heavy liquids indicate that they might have a sizeable effect on Tieschitz minerals. The age and⁸⁷Sr/⁸⁶Sr initial ratio as determined by handpicked separates are4.53 ± 0.06 b.y. and0.69880 ± 0.00020, indistinguishable from the whole-rock isochron.These results are interpreted as “primitive isochrons” dating the condensation of chondrites from the solar nebula. The best value of this event is given by joining both isochrons together at4.518 ± 0.026 b.y. and⁸⁷Sr/⁸⁶Sr= 0.69881 ± 0.00016. The near identity of this initial ratio with the one of Allende white inclusions argues in favor of a sharp isochronism of condensation from a⁸⁷Sr/⁸⁶Sr homogeneous nebula. Data from Guaren?a [11] and Richardton [48] are interpreted as secondary internal isochrons, 100 m.y. after the condensation of the whole rocks.The data are then used to constrain a thermal evolution model of the H chondrite parent body. This body might have a 150–175 km radius, and might have been heated by²⁶Al. An²⁶Al/²⁷Al ratio of 4–6 × 10^?6 is enough for heating such a body. Further tests for this model are proposed.     

Chronology and chemical history of the parent body of basaltic achondrites studied by the 87Rb-87Sr method

Total-rock ⁸⁷Rb-⁸⁷Sr measurements have been carried out on ten eucrites. Internal “isochrons” were determined for Ibitira, Bereba, Pasamonte, Stannern, Sioux County and Juvinas. Ibitira as well as Juvinas (previously published) give an age of 4.52 ± 0.25 b.y. The corresponding “ages” of Bereba and Sioux County are 4.17 ± 0.26 b.y. and 4.19 ± 0.14 b.y. Stannern and Pasamonte have maximum “ages” of 3.1 and 2.6 b.y., respectively. These last four “ages” are significantly lower than 4.55 b.y.Using the total rocks and the two primitive eucrites Ibitira and Juvinas, we define as the best differentiation age for eucrites 4.57 ± 0.13 b.y. which is better than any previous determination, and (⁸⁷Sr/⁸⁶Sr)_BABI = 0.69899 ± 0.00004. We discuss the early differentiation of the basaltic achondrite parent body by assuming that the parent body started with chondritic composition and had a two-step evolution during the very early history of the solar system.     

Weathering,Sr fluxes,and controls on water chemistry in the Lake Qinghai catchment,NE Tibetan Plateau

Strontium (Sr) concentrations and isotopic ratios have been measured in a series of water and rock samples from most of the major tributaries of the Lake Qinghai basin on the north‐eastern Tibetan Plateau. Dissolved Sr and ⁸⁷Sr/⁸⁶Sr show ranges of 488–12 240 nmol/l and 0·710497–0·716977, respectively. These data, together with measurements of major cations and anions in rivers and their tributaries and various lithologies of the catchment, were used to determine the contributions of Sr and its isotopic expense to rivers and lakes. Our results demonstrate that the chemical components and ⁸⁷Sr/⁸⁶Sr ratios of the alkaline waters are derived from mixing of carbonate and silicate sources, with the former contributing 72 ± 18% dissolved Sr to rivers. The difference in tributary compositions stems from the lithology of different river systems and low weathering intensity under a semi‐arid condition. Variation in ⁸⁷Sr/⁸⁶Sr ratios places constraint on the Sr‐isotopic compositions of the main tributaries surrounding Lake Qinghai. The water chemistry of the Buha River, the largest river within the catchment underlain by the late Paleozoic marine limestone and sandstones, dominates Sr isotopic composition of the lake water, being buffered by the waters from the other rivers and probably by groundwater. However, the characteristic chemical composition of the lake itself differs remarkably from the rivers, which can be attributed to precipitation of authigenic carbonates (low‐magnesium calcite, aragonite, and dolomite), though this does not impact the Sr isotope signature, which may remain a faithful indicator in paleo‐records. Regarding the potential role of groundwater input within the Lake Qinghai systems in the water budget and water chemistry, we have also determined the Sr concentration and ⁸⁷Sr/^S6Sr ratio of groundwater from diverse environments. This has allowed us to further constrain the Sr isotope systematic of this source. A steady‐state calculation gives an estimate for the groundwater flux of 0·19 ± 0·03 × 10⁸ m³/yr, accounting for about 8% of contemporary lake Sr budget. Copyright © 2010 John Wiley & Sons, Ltd.