Strontium isotope ratios in volcanic rocks from the south-eastern part of the Hellenic arc

Isotopic ratios of strontium in 9 volcanic rocks from the south-eastern part of the Hellenic arc range from 0.7037 to 0.7075. Within individual series of differentiation, there seems to be a correlation between Sr⁸⁷/Sr⁸⁶ and K₂O/SiO₂.All strontium isotope data for the Hellenic arc are reviewed. Comparable (but slightly smaller) ranges of Sr isotope ratios are found in other island arcs with continental basement. To explain the high values of Sr⁸⁷/Sr⁸⁶ ratio for the Hellenic arc, a selective addition of Sr⁸⁷ from the wall rock, and a process of assimilation involving water, perhaps from subducted sediments, are suggested. Since closely-spaced individual volcanic centres of similar ages have very different Sr isotope ratios, and since the range of Sr isotopic composition in individual centres is quite large, the variation is unlikely to be due to primary variation in mantle composition.     

Genesis of Sr Isotopes in Groundwater of Hebei Plain

To analyze the genesis of Sr isotopes in groundwater of Hebei plain, time-accumulative effect of 87Sr/86Sr ratio was studied. It is shown that 87Sr/86Sr ratio increases with the increasing age and depth of groundwater and has a positive correlation to 4Heexc and a negative correlation to δ18O and δD. The groundwater is divided into three groups to discuss the relation between 87Sr/86Sr ratio and Sr2 content: ① moderate Sr2 content and higher 87Sr/86Sr ratio (water I); ② lower Sr2 content and higher 87Sr/86Sr ratio (water II); and ③ higher Sr2 content and lower 87Sr/86Sr ratio (water III), that is hot water. On the basis of integrated analysis, it was considered that ① the radiogenic Sr in the Quaternary groundwater (Q4-Q1) originates from weathering of silicate rich in Na and Rb, mainly from plagioclase; ② the radiogenic Sr of hot water in Huanghua port is attributed to carbonate disso- lution, with lower 87Sr/86Sr ratio and higher Sr/Na ratio; ③ the recharge area is laterally recharged by the groundwater flowing through igneous and metamorphic rocks, with moderate 87Sr/86Sr ratio. How- ever, the formation mechanism of Sr isotopes in Tertiary groundwater needs further studies.     

Coupling of anatectic reactions and dissolution of accessory phases and the Sr and Nd isotope systematics of anatectic melts from a metasedimentary source

Advances in field observations and experimental petrology on anatectic products have motivated us to investigate the geochemical consequences of accessory mineral dissolution and nonmodal partial melting processes. Incorporation of apatite and monazite dissolution into a muscovite dehydration melting model allows us to examine the coupling of the Rb-Sr and Sm-Nd isotope systems in anatectic melts from a muscovite-bearing metasedimentary source. Modeling results show that (1) the Sm/Nd ratios and Nd isotopic compositions of the melts depend on the amount of apatite and monazite dissolved into the melt, and (2) the relative proportion of micas (muscovite and biotite) and feldspars (plagioclase and K-feldspar) that enter the melt is a key parameter determining the Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios of the melt. Furthermore, these two factors are not, in practice, independent. In general, nonmodal partial melting of a pelitic source results in melts following one of two paths in ε_Nd-⁸⁷Sr/⁸⁶Sr ratio space. A higher temperature, fluid-absent path (Path 1) represents those partial melting reactions in which muscovite/biotite dehydration and apatite but not monazite dissolution play a significant role; the melt will have elevated Rb/Sr, ⁸⁷Sr/⁸⁶Sr, Sm/Nd, and ε_Nd values. In contrast, a lower temperature, fluid-fluxed path (Path 2) represents those partial melting reactions in which muscovite/biotite dehydration plays an insignificant role and apatite but not monazite stays in the residue; the melt will have lower Rb/Sr, ⁸⁷Sr/⁸⁶Sr, Sm/Nd, and ε_Nd values than its source. The master variables controlling both accessory phase dissolution (and hence the Sm-Nd system), and melting reaction (and hence the Rb-Sr systematics) are temperature and water content. The complexity in Sr-Nd isotope systematics in metasediment-derived melts, as suggested in this study, will help us to better understand the petrogenesis for those granitic plutons that have a significant crustal source component.     

Strontium isotope composition and petrogenesis of the Kirkpatrick basalt,Queen Alexandra Range,Antarctica

The initial ⁸⁷Sr/⁸⁶Sr ratios of twelve basalt flows of Jurassic age on Storm Peak in the Queen Alexandra Range are anomalously high and range from 0.7094–0.7133. The average value is 0.7112±0.0013 (1). The concentrations of rubidium and strontium have arithmetic means of 60.6±19.4 ppm and 128.8±11.9 ppm, respectively. The corresponding average Rb/Sr ratio is 0.47 which is also anomalously high for rocks of basaltic composition. In addition, these rocks have high concentrations of SiO₂ (56.50%) and K₂O (1.29%) and are depleted in Al₂O₃ (12.92%), MgO (3.44%) and CaO (7.91%) compared to average continental tholeiites. They are nevertheless classified as basalts on the basis of the composition of microphenocrysts.The initial ⁸⁷Sr/⁸⁶Sr ratios and all of the chemical parameters of the flows exhibit systematic stratigraphic variations. These are interpreted as indicating the occurrence of four eruptive cycles. In a typical cycle the initial ⁸⁷Sr/⁸⁶Sr ratios of successive flows and their concentrations of SiO₂, FeO (total iron), Na₂O, K₂O, P₂O₅, Rb and Sr decrease in ascending stratigraphic sequence while the concentrations of TiO₂, Al₂O₃, MgO, CaO and MnO increase upward. The initial ⁸⁷Sr/⁸⁶Sr ratios of the flows show a strong positive correlation with the strontium concentration. Similar correlations are observed between the initial ⁸⁷Sr/⁸⁶Sr ratios and all of the major oxide components. These relationships are incompatible with the hypothesis that these flows are the products of crystal fractionation of a-34 magma at depth under closed-system conditions. It is suggested that the flows resulted from the hybridization of a normal tholeiite basalt magma by assimilation of varying amounts of granitic rocks in the Precambrian basement which underlies the entire Transantarctic Mountain chain.Mixtures of two components having different ⁸⁷Sr/⁸⁶Sr ratios and differing strontium concentrations are related to each other by hyperbolic mixing equation. Such an equation was fitted by least squares regression of data points to a straight line in coordinates of initial ⁸⁷Sr/⁸⁶Sr and the reciprocals of the concentrations of strontium. This equation and plots of strontium versus other oxides were then used to estimate the chemical composition of the parent basalt magma and of the granitic contaminant by substituting reasonable estimates of their ⁸⁷Sr/⁸⁶Sr ratios. The chemical composition of the parent basalt (⁸⁷Sr/⁸⁶Sr=0.706) is generally compatible with that of average continental tholeiite, but is distinctive by having a low concentration of strontium (117 ppm). The chemical composition of the contaminant (⁸⁷Sr/⁸⁶Sr=0.720) is enriched in strontium (173 ppm), SiO₂, FeO (total iron) and the alkalies but is depleted in Al₂O₃, MgO and CaO. The data for strontium indicate that the lava flows on Storm Peak contain between 20 and 40% of this granitic contaminant. The contamination of basalt magma is not a local event but is characteristic of the Jurassic basalt flows and diabase sills throughout the Transantarctic Mountains and in Tasmania.Laboratory for Isotope Geology and Geochemistry, Contribution No. 33.     

川东北普光气田下三叠统飞仙关组白云岩成因——来自岩石结构与Sr同位素和Sr含量的证据

研究了川东北普光气田下三叠统飞仙关组白云岩储层的岩石结构Sr的含量和Sr同位素组成,讨论了它的成因,飞仙关组优质储层为成岩期埋藏交代白云化作用的产物,来自岩石结构和Sr同位素和Sr含量的证据包括如下几个方面:(1)与准同生白云岩比较,埋藏白云岩的岩石结构和Sr同位素和Sr含量地球化学特征与前者有显著差别;(2)飞仙关组所有各类碳酸盐岩(或矿物)具有早三叠世海水Sr同位素组成特征,~(87)Sr/~(86)Sr比值变化范围为0.706588～0.708187,覆盖了全球早三叠世海水Sr同位素的变化范围(0.7076～0.7078),平均值0.707656与全球早三叠世平均值(0.707743)基本一致;(3)埋藏白云岩~(87)Sr/86Sr比值变化范围为0.707122～0.707419,平均值0.707421,都略低于全球早三叠世海水Sr同位素变化范围和平均值,但与已报道的川东北早三叠世飞仙关期海水Sr同位素变化范围(0.707330～0.707383)和平均值(0.707350)都非常接近,说明白云石化流体具有强烈的川东北地区早三叠世飞仙关期海水Sr同位素组成特征;(4)综合岩石结构、Sr同位素和Sr含量地球化学特征,证明飞仙关组白云岩储层为成岩期埋藏交代作用产物,白云石化流体来自地层中高Sr和高盐度的海源地层水.     

Isotope hydrology of the Chalk River Laboratories site,Ontario, Canada

This paper presents results of hydrochemical and isotopic analyses of groundwater (fracture water) and porewater, and physical property and water content measurements of bedrock core at the Chalk River Laboratories (CRL) site in Ontario. Density and water contents were determined and water-loss porosity values were calculated for core samples. Average and standard deviations of density and water-loss porosity of 50 core samples from four boreholes are 2.73 ± 12 g/cc and 1.32 ± 1.24 percent. Respective median values are 2.68 and 0.83 indicating a positive skewness in the distributions. Groundwater samples from four deep boreholes were analyzed for strontium (⁸⁷Sr/⁸⁶Sr) and uranium (²³⁴U/²³⁸U) isotope ratios. Oxygen and hydrogen isotope analyses and selected solute concentrations determined by CRL are included for comparison. Groundwater from borehole CRG-1 in a zone between approximately +60 and −240 m elevation is relatively depleted in δ¹⁸O and δ²H perhaps reflecting a slug of water recharged during colder climatic conditions. Porewater was extracted from core samples by centrifugation and analyzed for major dissolved ions and for strontium and uranium isotopes. On average, the extracted water contains 15 times larger concentration of solutes than the groundwater. ²³⁴U/²³⁸U and correlation of ⁸⁷Sr/⁸⁶Sr with Rb/Sr values indicate that the porewater may be substantially older than the groundwater. Results of this study show that the Precambrian gneisses at Chalk River are similar in physical properties and hydrochemical aspects to crystalline rocks being considered for the construction of nuclear waste repositories in other regions.     

Hydrogeochemistry and strontium isotopes of spring and mineral waters from Monte Vulture volcano,Italy

This paper describes the results of a study that was conducted to determine the relationship between hydrogeochemical composition and ⁸⁷Sr/⁸⁶Sr isotope ratios of the Mt. Vulture spring waters. Forty samples of spring waters were collected from local outcrops of Quaternary volcanites. Physico-chemical parameters were measured in the field and analyses completed for major and minor elements and ⁸⁷Sr/⁸⁶Sr isotopic ratios. A range of water types was distinguished varying from alkaline-earth bicarbonate waters, reflecting less intense water–rock interaction processes to alkali bicarbonate waters, probably representing interaction with volcanic rocks of Mt. Vulture and marine evaporites. The average ⁸⁷Sr/⁸⁶Sr isotope ratios suggest at least 3 different sources. However, some samples have average Sr isotope ratios (0.70704–0.70778) well above those of the volcanites. These ratios imply interaction with other rocks having higher ⁸⁷Sr/⁸⁶Sr ratios, probably Triassic evaporites, which is substantiated by their higher content of Na, SO₄ and Cl. The Sr isotope ratios for some samples (e.g. Toka and Traficante) are intermediate between the value for the Vulture volcanites and that for the local Mesozoic rocks. The salt content of these samples also lies between the value for waters interacting solely with the volcanites and the value measured in the more saline samples. These waters are thus assumed to result from the mixing of waters circulating in volcanic rocks with waters presumably interacting with the sedimentary bedrock (marine evaporites).     

广西钦州石炭-二叠纪深海硅质岩的锶同位素组成及其地质意义

报道了广西钦州海槽早石炭世-早二叠世深水硅质岩的锶同位素测定结果和经年代校正后的87Sr/86Sr初始值,建立了锶同位素演化曲线;通过与同时代上扬子地区台地相碳酸盐岩87Sr/86Sr比值和演化曲线的对比,研究了二者的异同和造成差异的原因。深水硅质岩和同期台地相碳酸盐岩的锶同位素演化曲线在总体特征上具有一定的相似性,反映海平面变化对其影响的一致性。玄武岩喷发等局部事件和硅质岩中无法回避的陆源碎屑的影响是造成87Sr/86Sr比值和演化曲线差异的主要原因。硅质岩锶同位素演化曲线显示,海平面上升发生于早石炭世,在晚石炭世早期达到最大值,晚石炭世晚期,海平面有所下降,在其后的早二叠世,海平面再次上升。     

The RbSr age dating of some Carboniferous shales

The RbSr age dating method has been applied to a sequence of Carboniferous shales for which some geochemical information was already available. In the marine shales, the Rb/Sr ratio is higher than in the non-marine and brackish water shales. Although the range of values can be attributed to depositional processes, the range of Rb/Sr values is too small to give a depositional isochron, and thus the age of deposition can not be determined. If samples with a variable mineralogy had been selected for the isotope study, the range of Rb/Sr could have been extended. Only by chance, however, would the depositional age have been obtained.A comparison of the RbSr isotope values in the Carboniferous shales with those in probable source rocks shows that a reduction in the Sr⁸⁷/Sr⁸⁶ ratio relative to the Rb⁸⁷/Sr⁸⁶ ratio may have taken place. Such a reduction could have occurred on the Carboniferous land-mass during the formation of the clay minerals.     

Role of Subsurface Brines in Salt Balance: The Case Study of the Caspian Sea and Kara Bogaz Bay

The water level of the Caspian Sea fluctuated significantly during recent history, without consensus for the cause. The varied chemistry of the Caspian, Kara Bogaz and sediment a interstitial waters provides a further insight. Element concentrations and ⁸⁷Sr/⁸⁶Sr ratios of the interstitial waters were compared to those of Caspian and Kara Bogaz open waters, and of acid-leached extractable components. The ⁸⁷Sr/⁸⁶Sr ratios of the interstitial waters are explained by addition of subterranean waters similar to nearby spring waters. These subterranean waters yield chemical characteristics such as a Cl/SO₄, ⁸⁷Sr/⁸⁶Sr, Ca/Sr and K/Rb ratios of respectively 80, 0.7086, 250 and 1,800. However, their addition does not explain the large difference in the K/Rb ratio of the Caspian and Kara Bogaz waters, respectively at 7,630 and 17,550, which implies also a leaching of salt deposits by the upward migrating subterranean waters. The sediments of the southern Caspian basin, with low Na, Cl and SO₄ in their interstitial waters, deposited apparently in an anoxic environment. The related chemical changes in the waters are also indicative of a recent change in the hydrologic regime, possibly induced by a changing morphology of the drainage basin.     

A strontium isotope and trace element profile through the Partridge River Troctolite,Duluth complex,Minnesota

Initial ⁸⁷Sr/⁸⁶Sr ratios down a 2,315 foot-long core (DDH-295) through the Partridge River Troctolite are lower in the depth range 710–1,410 feet (0.70443±22) than in the underlying and overlying rocks (0.70500±18). These initial ratio variations define three zones (I, II, and III) thought to be three intrusive units within the troctolite. The best estimate of the Rb-Sr age of the troctolite is 1,050±105 m.y. The olivine compositions and the abundances of the incompatible trace elements Zr, Y, and Rb show identical variations down the core, with downward repetitions of olivine iron-enrichment and incompatible trace element enrichments. Discontinuities in the olivine compositions and incompatible trace element abundances match the initial ⁸⁷Sr/⁸⁶Sr ratio discontinuities in the core. The strontium isotope data imply that involatile components of the Proterozoic Virginia Formation and other Archaean rocks were not significantly assimilated by the troctolites, for only three out of the twenty-three initial ⁸⁷Sr/⁸⁶Sr ratios depart from normal magmatic values. These three anomalous ratios are not systematically related to the Cu-Ni sulphide mineralization and may be the result of secondary calcite in the troctolite. The strontium isotope systematics of the Virginia Formation xenoliths and underlying hornfelses are highly disturbed as a result of Rb loss. The apparently inverted fractionation sequences in the troctolites are interpreted in terms of downward increases in intercumulus liquid in repeated magma batches and controlled by plagioclase flotation. The amount of intercumulus liquid is estimated to range from 7 to 61 weight per cent. The Cu-Ni sulphides are concentrated in the lower 250 feet of zone I (immediately above the Virginia Formation) and through 400 feet of core across the contact between zones I and II, more than 750 feet above the base. Because the sulphide-bearing troctolites are not systematically related to disturbances in the magmatic initial ⁸⁷Sr/⁸⁶Sr ratios, the mineralization probably involved the volatile transfer of sulphur derived from dehydration reactions in the underlying Virginia Formation.     

Strontium and oxygen isotope decoupling in the Hercynian Trois Seigneurs Massif,Pyrenees: evidence for fluid circulation in a brittle regime

Systematic shifts of oxygen isotopic compositions in the higher grade parts of the high temperature-low pressure Hercynian metamorphic sequence, exposed in the Trois Seigneurs Massif, have previously been explained as a result of an influx of surface-derived water during the prograde part of the metamorphic cycle. It has been suggested that this caused a regional lowering of ⁸⁷Sr/⁸⁶Sr in the metamorphic sequence. Mapping of strontium isotopic compositions across a 15 m meta-carbonate horizon in the higher grade pelite-psammite sequence shows that strontium isotopic compositions were homogenised over length scales of metres or less during the Hercynian metamorphism, which brought the carbonate and pelite-psammite to oxygen isotopic equilibrium with a common fluid. Comparison of model pre-Hercynian ⁸⁷Sr/⁸⁶Sr profiles across the carbonate (based on a depositional/diagenetic age of 450 Ma and initial ⁸⁷Sr/⁸⁶Sr ratio of 0.7086 given by 10 m length scale averaging) with the post-Hercynian ⁸⁷Sr/⁸⁶Sr profile (calculated from analysed ⁸⁷Sr/⁸⁶Sr and Rb/Sr compositions) implies strontium isotopic diffusion distances of ca. 0.4 m in the carbonate and ca. 7 m in the pelite-psammite. The limited Sr-isotopic diffusion distance of 0.4–0.7 m within the carbonate is compatible with pervasive oxygen-isotopic exchange over distances restricted to 4–15 m if fluid strontium concentrations were between 4 and 50 ppm. The strontium isotopic transport distances are not compatible with pervasive oxygen isotopic alteration over the observed 5 km regional scale. Either the flow was perfectly layer-parallel or, more probably, the regional-scale alteration of oxygen took place by fluid circulation in the brittle regime early in, or prior to, the Hercynian metamorphic event. Flow along cracks with incomplete diffusive exchange between fluid and wall rock would allow greater decoupling of oxygen and strontium isotopic transport than pervasive advective transport with local fluid-solid equilibrium.     

Use of Sr isotopes as a tool to decipher the soil weathering processes in a tropical river catchment,southwestern India

River water composition (major ion and ⁸⁷Sr/⁸⁶Sr ratio) was monitored on a monthly basis over a period of three years from a mountainous river (Nethravati River) of southwestern India. The total dissolved solid (TDS) concentration is relatively low (46 mg L⁻¹) with silica being the dominant contributor. The basin is characterised by lower dissolved Sr concentration (avg. 150 nmol L⁻¹), with radiogenic ⁸⁷Sr/⁸⁶Sr isotopic ratios (avg. 0.72041 at outlet). The composition of Sr and ⁸⁷Sr/⁸⁶Sr and their correlation with silicate derived cations in the river basin reveal that their dominant source is from the radiogenic silicate rock minerals. Their composition in the stream is controlled by a combination of physical and chemical weathering occurring in the basin. The molar ratio of SiO₂/Ca and ⁸⁷Sr/⁸⁶Sr isotopic ratio show strong seasonal variation in the river water, i.e., low SiO₂/Ca ratio with radiogenic isotopes during non-monsoon and higher SiO₂/Ca with less radiogenic isotopes during monsoon season. Whereas, the seasonal variation of Rb/Sr ratio in the stream water is not significant suggesting that change in the mineral phase being involved in the weathering reaction could be unlikely for the observed molar SiO₂/Ca and ⁸⁷Sr/⁸⁶Sr isotope variation in river water. Therefore, the shift in the stream water chemical composition could be attributed to contribution of ground water which is in contact with the bedrock (weathering front) during non-monsoon and weathering of secondary soil minerals in the regolith layer during monsoon. The secondary soil mineral weathering leads to limited silicate cation and enhanced silica fluxes in the Nethravati river basin.     

Rb-Sr isochron study of the Thorr and Main Donegal Granites,Ireland

A Rb-Sr whole-rock isochron study indicates that the entire Donegal granite suite was emplaced into orthotectonic Caledonian (Dalradian) rocks over a short interval during mid-Silurian to earliest-Devonian times. The Thorr pluton, probably the earliest member of the suite, yields an age of 418 ± 26 Myr and initial ⁸⁷Sr/⁸⁶Sr ratio of 0·7055 ± 4, while the latest member, the Main Donegal pluton has an age of 407 ± 23 Myr and initial ⁸⁷Sr/⁸⁶Sr ratio of 0·7063 ± 5 (Λ⁸⁷Rb = 1·42 ± 10⁻¹¹ yr⁻¹). Errors on both the age and initial Sr isotope ratios incorporate both a priori and geological scatter components and are quoted at the 2-sigma level. The low and restricted range of initial Sr isotope ratios suggests small but significant differences in the composition of the parental granitic magmas which were derived from a low Rb/Sr, low ⁸⁷Sr/⁸⁶Sr source.     

Constraining the marine strontium budget with natural strontium isotope fractionations (Sr/Sr∗, δSr) of carbonates, hydrothermal solutions and river waters

We present strontium (Sr) isotope ratios that, unlike traditional ⁸⁷Sr/⁸⁶Sr data, are not normalized to a fixed ⁸⁸Sr/⁸⁶Sr ratio of 8.375209 (defined as δ^88/86Sr = 0 relative to NIST SRM 987). Instead, we correct for isotope fractionation during mass spectrometry with a ⁸⁷Sr-⁸⁴Sr double spike. This technique yields two independent ratios for ⁸⁷Sr/⁸⁶Sr and ⁸⁸Sr/⁸⁶Sr that are reported as (⁸⁷Sr/⁸⁶Sr∗) and (δ^88/86Sr), respectively. The difference between the traditional radiogenic (⁸⁷Sr/⁸⁶Sr normalized to ⁸⁸Sr/⁸⁶Sr = 8.375209) and the new ⁸⁷Sr/⁸⁶Sr∗ values reflect natural mass-dependent isotope fractionation. In order to constrain glacial/interglacial changes in the marine Sr budget we compare the isotope composition of modern seawater ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_Seawater) and modern marine biogenic carbonates ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_Carbonates) with the corresponding values of river waters ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_River) and hydrothermal solutions ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_HydEnd) in a triple isotope plot. The measured (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_River values of selected rivers that together account for ∼18% of the global Sr discharge yield a Sr flux-weighted mean of (0.7114(8), 0.315(8)‰). The average (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_HydEnd values for hydrothermal solutions from the Atlantic Ocean are (0.7045(5), 0.27(3)‰). In contrast, the (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_Carbonates values representing the marine Sr output are (0.70926(2), 0.21(2)‰). We estimate the modern Sr isotope composition of the sources at (0.7106(8), 0.310(8)‰). The difference between the estimated (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_input and (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_output values reflects isotope disequilibrium with respect to Sr inputs and outputs. In contrast to the modern ocean, isotope equilibrium between inputs and outputs during the last glacial maximum (10-30 ka before present) can be explained by invoking three times higher Sr inputs from a uniquely “glacial” source: weathering of shelf carbonates exposed at low sea levels. Our data are also consistent with the “weathering peak” hypothesis that invokes enhanced Sr inputs resulting from weathering of post-glacial exposure of abundant fine-grained material.     

云南含罗平生物群层位锶同位素组成与演化

现有公布的数据显示,海水87Sr/86Sr值在中三叠世安尼期较为平稳,有别于早三叠世因环境导致的动荡变化,为二叠纪末生物大灭绝之后生物复苏的加速期,而罗平生物群就是该加速期的标志性生物群。本文研究了含罗平生物群层位标准剖面-大凹子剖面上连续沉积的26件碳酸盐岩样品的锶同位素组成与演化,用于了解含罗平生物群层位沉积海水锶同位素的变化趋势。结果显示:(1)碳酸盐岩中Sr平均值大于2000×10-6,主要来自于文石和海洋成岩作用;(2)低Mn和Mn/Sr0.4说明:87Sr/86Sr数据在很大程度上能代表同时期海水中的87Sr/86Sr比值;(3)这些样品的87Sr/86Sr值变化在0.707969～0.708253,平均值为0.708025,锶同位素比值变化曲线呈小幅度的起伏波动,其值明显大于同时期欧洲等地公布的数据,但同华南其他地区公布的数据具有相似性,推测含罗平生物群层位锶同位素组成仅代表区域事件,受印支运动影响。     

山西省襄汾县陶寺遗址出土动物牙釉质的锶同位素比值分析

锶同位素分析技术已经成为国际考古学界用于探索人和动物迁移活动的主要方法.陶寺遗址位于山西省襄汾县陶寺镇,距今4500～3900年,是目前我国规模最大的、显现文明化程度最高的史前聚落遗址之一.文章通过热电离质谱分析方法对山西襄汾县陶寺镇陶寺遗址龙山晚期出土动物的14个动物牙釉质的锶同位素比值进行了测定.研究结果表明,5个...     

The isotopic composition of strontium in non-marine carbonate rocks: the Flagstaff Formation of Utah*

The isotopic composition of strontium in surface water in continental basins is determined primarily by the geology of the basin and to a lesser extent by climatic conditions. Consequently, the ⁸⁷Sr/⁸⁶Sr ratios of brines in such basins can change only as a result of changes in the geology or climate. This principle of isotope geology was studied by analysis of a suite of non-marine carbonate rocks from the Flagstaff Formation (Palaeocene-Eocene) of Utah. The samples were collected from a section in Fairview Canyon of Sanpete County. They include both limestone and dolomite and were selected to have low non-carbonate residues. The concentrations of strontium in calcites averages 383 ± 128 p.p.m., while those of dolomites increase from 354 ± 74 p.p.m. in the lower 43 m of section to a maximum of 2259 p.p.m. higher up. The increase in the strontium content of dolomite is interpreted as evidence for a change from steady-state to progressively more evaporitic conditions. Two dolomites have isotopic compositions of oxygen expressed as δ¹⁸O = -2.75‰ (relative to the PDB standard) and are enriched in ¹⁸O relative to two calcites whose average δ¹⁸O value is -9.9‰. The ⁸⁷Sr/⁸⁶Sr ratios of the carbonate minerals range from 0.70890 to 0.71260. These values are clearly greater than the ⁸⁷Sr/⁸⁶Sr ratio of marine carbonates of Early Eocene age which is 0.70744. The variation of the ⁸⁷Sr/⁸⁶Sr ratio in this section of the Flagstaff Formation is real and reflects the occurrence of geological events which changed the isotopic composition of Sr entering Lake Flagstaff. The non-carbonate fractions of six carbonate rocks and one sandstone fit a straight line on the strontium mixing diagram in co-ordinates of initial ⁸⁷Sr/⁸⁶Sr and 1/Sr concentration. These results suggest that the isotopic composition of strontium in Lake Flagstaff may have been modulated by periodic input of volcanogenic detritus of felsic composition.     

高Rb/Sr岩石样品中Sr同位素多接收等离子体质谱分析校正方法研究

在利用多接收电感耦合等离子体质谱(MC-ICPMS)进行Sr同位素研究中,⁸⁷Rb对于⁸⁷Sr干扰严重。岩石样品经化学分离后,若Rb/Sr≤0.0005,可以采用传统的Rb干扰扣除方法对⁸⁷Sr/⁸⁶Sr测定值进行准确校正;但如果样品经化学分离后仍含有较高的Rb/Sr比,同量异位素的干扰不能完全消除,则无法准确校正⁸⁷Sr/⁸⁶Sr测定值,直接影响测试结果的准确度。本文针对Rb含量较高的地质样品设计两组实验,确定了⁸⁷Sr/⁸⁶Sr同位素比值与Rb/Sr元素含量比值的关系曲线,并在理论分析的基础上,提出包含同位素分馏校正在内的重叠干扰校正方法。通过实际地质样品验证,该校正方法在较高含量Rb元素共存(Rb/Sr<0.2)的Sr纯化液中,能够较为准确地测量⁸⁷Sr/⁸⁶Sr同位素比值,降低了MC-ICPMS分析地质样品中Sr同位素时对化学分离步骤的要求。而对于Rb/Sr>0.2的地质样品,因仪器分馏效应和记忆效应影响,测试精确度大大降低,无论采用何种校正方法均无法得到准确的Sr同位素组成。     

Correlation between strontium and oxygen isotopic compositions of rocks from the Adamello massif (Northern Italy)

Rock samples from the lithologic units forming the Adamello massif were analyzed for Rb and Sr concentrations and for⁸⁷Sr/⁸⁶Sr and¹⁸O/¹⁶O ratios. The most important features are as follows:

1. the strontium and oxygen isotopes show a systematic variation from south to northwest across the massif, the older units in the south being lower both in⁸⁷Sr and¹⁸O;
2. a good positive correlation was found between strontium and oxygen isotopic compositions.

Two genetic models are advanced for explaining the results: (1) the mixing of two magmas with different¹⁸O and⁸⁷Sr contents; (2) magma formation at different depths in a crust layered with respect to both oxygen and strontium isotope composition.