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1.
87Sr86Sr ratios have been determined in fifteen volcanic rocks from the northwestern part of the Hellenic arc. They range from 0.7041 to 0.7134. There is no apparent correlation of strontium isotope values with any major chemical component or with Rb/Sr ratios. The 87Sr86Sr ratios appear to increase in a general way with increasing depth to the Benioff zone. The strontium isotope ratios are higher than from most island arcs; this is believed to be due to contamination.  相似文献   

2.
Fresh basalt and metabasalt dredged from the Mid-Atlantic Ridge were studied for Na, K, Rb, Sr, and H2O(+) contents, and strontium and hydrogen isotope ratios. Na, K, Rb, and Sr contents of these samples are within the range of those of oceanic tholeiite. H2O(+) content, strontium, and hydrogen isotope ratios vary widely. The variation in water content of metabasalt is apparently related to the chlorite content. The metamorphic temperature was about 550 °C based on the estimated δD value of chlorite. There is positive linear relationship between water content and strontium isotope ratio. Based on this relationship, the variation of strontium isotope ratio of the metabasalt was interpreted as follows: complete exchange occurred between strontium in the chlorite portion of the metabasalt and strontium in sea water (87Sr/86Sr ratio=0.7090), while the original strontium (87Sr/86Sr∼0.7023) was retained in the non-altered portion of the basalts.  相似文献   

3.
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。  相似文献   

4.
郑荣才  文华国  郑超  罗平  李国军  陈守春 《岩石学报》2009,25(10):2459-2468
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.  相似文献   

5.
《Applied Geochemistry》2006,21(10):1626-1634
Mineral waters in Britain show a wide range of 87Sr/86Sr isotope compositions ranging between 87Sr/86Sr = 0.7059 from Carboniferous volcanic rock sources in Dunbartonshire, Scotland to 87Sr/86Sr = 0.7207 in the Dalradian aquifer of Aberdeenshire, Scotland. The 87Sr/86Sr composition of the waters shows a general correlation with the aquifer rocks, resulting in the waters from older rocks having a more radiogenic signature than those from younger rocks. This wide range of values means that the Sr isotope composition of mineral water has applications in a number of types of studies. In the modern commercial context, it provides a way of fingerprinting the various mineral waters and hence provides a method for recognising and reducing fraud. From an environmental perspective, it provides the first spatial distribution of bio-available 87Sr/86Sr in Britain that can be used in modern, historical and archaeological studies.  相似文献   

6.
《Applied Geochemistry》2003,18(1):117-125
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).  相似文献   

7.
Twelve whole-rock samples of volcanic rocks and a composite of 11 basanitoid samples from Ross Island and vicinity, Antarctica show a narrow range of 87Sr/86Sr ratios from 0.70305 to 0.70339. This range is consistent with a model of differentiation from a single parent magma, but the data allow a 30% variation in the 87Rb/86Sr ratio in the source region if the average ratio is less than 0.057 and if the source region has existed as a closed system for 1.5 b.y. Megacrysts of titaniferous augite, kaersutite, and anorthoclase are isotopically indistinguishable from the host volcanic rocks and therefore are probably cogenetic with the volcanic sequence. A single trachyte sample is isotopically distinct from the rest of the volcanic rocks and probably was contaminated with crustal strontium.Ultramafic and mafic nodules found in association with basanitoids and trachybasalts have 87Sr/86Sr ratios ranging from 0.70275 to 0.70575. Several of these nodules exhibit evidence of reaction with the melt and are isotopically indistinguishable from their hosts, but data for seven granulite-facies nodules show an apparent isochronal relationship. Although this isochron may be fortuitous, the resulting age of 158±22 m.y. is similar to ages reported for the voluminous Ferrar Dolerites, and suggests isotopic re-equilibration within the lower crust and upper mantle. These nodules are not genetically related to the Ferrar Dolerites, as evidenced by their lower initial 87Sr/86Sr ratios.Three ultramafic nodules are texturally and isotopically distinct from the rest of the analyzed nodules. These are friable, have larger 87Sr/86Sr ratios, and may represent a deeper sampling of mantle rock than the granulite-facies nodules. They were, however, derived at a shallower depth than the alkalic magma. Thus they are not genetically related to either the magma or the granulite-facies nodules.  相似文献   

8.
Strontium isotopic studies of kimberlites reveal no significant differences between the respective whole-rock Sr87/Sr86 ratios of fissure and pipe kimberlites. Kimberlites from the Swartruggens fissure (calcareous micaceous kimberlite) have Sr87/Sr86 ratios of from 0.709 to 0.716, whilst those from the Wesselton pipe have Sr87/Sr86 ratios of from 0.708 to 0.715. Other kimberlites range from 0.706 to 0.715. Samples are considered to be late Cretaceous to early Tertiary and thus the ratios are approximately initial ratios. The Sr87/Sr86 ratios bear no relation to the Rb or Sr content of individual kimberlite bodies. The high initial ratios are not due to bulk assimilation of granitic material in either a kimberlite or carbonatitic magma. Rb-Sr data for garnet peridotites and eclogite xenoliths in kimberlite are not compatible with production of kimberlite by eclogite fractionation from a melt derived from garnet lherzolite. The Sr isotopic composition of kimberlite is compatible with partial melting of garnet mica peridotite. The isotopic composition of liquids formed by partial melting of this rock can be modified by (i) gross contamination with material of low Sr87/Sr86 ratio or (ii) selective diffusion of material of high Sr87/Sr86 ratio into kimberlitic fluids.  相似文献   

9.
Thirty-one selected volcanic rocks from the Myoko volcano group which comprises a volcanic chain of four independent volcanoes of Quaternary to Recent age are analyzed for 87Sr/86Sr ratios. The rocks of the lizuna volcano, the oldest among the Myoko volcano group, have higher 87Sr/86Sr ratios and show a larger scatter ranging from 0.70437 to 0.70556 than those of other volcanoes. The Kurohime volcanic rocks have a restricted range of 87Sr/86Sr ratios (0.70403∼0.70435). 87Sr/86Sr ratios of the Myoko volcanic rocks are almost the same in average to those of the Kurohime volcanic rocks, although somewhat varied ranging from 0.70378 to 0.70461. A single analysis of the Yakeyama volcanic rock yielded a 87Sr/86Sr ratio of 0.70427. A characteristic pattern in 87Sr/86Sr ratios is observed through the volcanic activity of the Myoko volcano group; 87Sr/86Sr ratios are high in the early stage of the volcanic activity and then decrease to low values, the late eruptives being characterized by constant 87Sr/86Sr ratios. The negative correlation between 87Sr/86Sr and Rb/Sr, and positive correlation between 87Sr/86Sr and Sr found in the rocks of the Iizuna volcano are interpreted to show the occurrence of contamination by materials with high 87Sr/86Sr ratios (>0.7056), low Rb/Sr ratios (<0.01) and high Sr contents (>300 ppm). Sialic crustal contamination may have played only a minor role.  相似文献   

10.
The epithermal Au-Ag Shkol'noe deposit is located in the Kandjol ore field, Kurama Mountains. This region is a part of the east-west trending Late Hercynian Bel'tau-Kurama volcanic belt, an Andean-style collisional margin. The deposit comprises a number of quartz-carbonate veins hosted by the syn-subductional Middle Carboniferous Karamazar granodiorites. The Au-Ag mineralization is considered to be the result of the earliest hydrothermal event in the region. The Rb-Sr isochron age 296.3 ± 1.3 Ma and an initial 87Sr/86Sr0=0.7071 ± 2 ratio were obtained for an adularia-sericite-quartz-calcite sample from Au-Ag mineralization. The 87Sr/86Sr ratio range from 0.70645 ± 10 to 0.70741 ± 10 was obtained for the calcites from the earlier and later mineral assemblages. The Rb-Sr age is interpreted as a real geological age of the Au-Ag mineralization. It corresponds to the initial stage of the Late Carboniferous – Early Permian collision following the main syn-subduction stage of Bel'tau-Kurama volcanic belt evolution. The comparison of the Rb-Sr age with previously obtained 40Ar-39Ar and K-Ar data for adularia from the Au-Ag mineralization implies that gangue minerals of the Shkol'noe deposit bears the fingerprint of at least three events in its history. They are (1) Au-Ag mineralization at 296.3 ± 1.3 Ma; and (2) two subsequent thermal pulses at 277 ± 4 and 263–267 ± 8 Ma. The minimum time scale for the hydrothermal activity within the Shkol'noe deposit is thus approximately 30 million years. A general uniformity of the strontium source during the hydrothermal processes within the Au-Ag Shkol'noe deposit (87Sr/86Sr0=0.70645 ± 10 to 0.70741 ± 10) is suggested as well as within the Bel'tau-Kurama belt (87Sr/86Sr0=0.7051–0.707). The slight shift into a higher strontium isotope composition of the hydrothermal minerals of the Shkol'noe deposit in comparison with other deposits and rocks of the Bel'tau-Kurama belt may be ascribed to the contribution of relatively radiogenic strontium from the Karamazar-type granitoids. The mobilization of low radiogenic strontium during propylitic alteration of diabase dikes emplaced after the Au-Ag mineralization could be responsible for comparatively low 87Sr/86Sr ratios in some of the latest post-dike carbonates. Received: 4 August 1998 / Accepted: 25 August 1998  相似文献   

11.
The present-day North Chilean Coastal Cordillera between 18°30′S and 22°S records an important part of the magmatic evolution of the Central Andes during the Jurassic. Calc-alkaline to subordinate tholeiitic members from four rock groups with biostratigraphically constrained age display incompatible element pattern characteristic of convergent plate-margin volcanism, whereas alkaline basalts of one group occurring in the Precordillera show OIB-type trace element signatures. The correlation of biostratigraphic ages, regional distribution, and composition of the volcanic rocks provides a basis for the discussion on geochemical evolution and isotope ratios.Major and trace element distributions of the volcanic rocks indicate their derivation from mantle-derived melts. LILE and LREE enrichments in calc-alkaline basaltic andesites to dacites and some of the tholeiites hint at the involvement of hydrous fluids during melting and mobile element transport processes. A part of the Early Bajocian to ?Lower Jurassic and Oxfordian andesites and dacites are adakite-like rocks with a substantial participation of slab melt and are characterized by high Sr/Y ratios and low HREE contents. The Middle Jurassic tholeiitic and calc-alkaline basalts and basaltic andesites have been transported and partly stored within a system of deep-seated feeder fissures and crustal strike-slip faults before eruption.The isotopic composition of Sr (87Sr/86Sri=0.7032-0.7056) and Nd (εNdi=2.2-7.1) of the Jurassic volcanic rocks mostly fall in the range characteristic for mantle melts although some crustal components may have been involved. A few samples show slightly more radiogenic Sr isotopic composition, which is probably due to interaction with ancient sea-water. The Pb isotopic composition of the arc rocks is uncoupled from the isotopic composition of Sr and Nd and is dominated by the crustal component. Since the Cretaceous and Modern arc volcanic rocks show Pb isotopic compositions that can be largely explained by in situ Pb isotope growth of Jurassic arc volcanic rocks, we argue that the various Andean arc systems between 18°30′S and 22°S formed on the same type of basement.Most of the investigated samples have high Ba, Zr, and Th concentrations compared to island arc mafic volcanic rocks. About 20% of the Jurassic arc volcanics comprise of dacitic to rhyolitic rocks. These characteristics combined with the Pb isotopic composition that shows the influence of a Palaeozoic (or partly older) basement point to a continental margin setting for the North Chilean Jurassic arc. The distribution of the magmatic rocks throughout time, their textures, and the character of intercalated sedimentary rocks reflect westward movement of the magma sources and of the arc/back-arc boundary relative to the current coast line during the Early Bajocian on a broad front between 19°30′ and 21°S.  相似文献   

12.
Mineral chemistry, major and trace elements, and 87Sr/86Sr ratios are presented for 29 igneous rocks dredged from the northern portion of the Izu-Ogasawara arc. These rocks are compositionally bimodal. Basement gabbro and trondhjemite from the arc are extremely poor in K2O (0.05–0.19%) and Rb (0.48–0.62 ppm), and their REE patterns and Sr isotope ratios indicate that there are island arc tholeiites. Quaternary volcanic rocks from the present volcanic front (Shichito Ridge; active arc), back-arc seamounts (east side; inactive arc) and Torishima knoll between the two back-arc depressions (incipient back-arc basins) behind the active arc have the same geochemical characteristics as the above plutonic rocks though they are not as depleted in K and Rb. Rhyolite pumice from the backarc depression is also the depleted island arc tholeiite, whereas basalts from the depression have compositions that are transitional between MORB and island arc tholeiites in trace element (Ti, Ni, Cr, V, Y and Zr) and mineral chemistries. The back-arc depression basalts have relatively high BaN/CeN(0.66–1.24), Cen/YbN(1.1–1.9) and K/Ba(45–105) and low 87Sr/86Sr (0.70302–0.70332) and Ba/Sr (0.1–0.2), which are similar to other back-arc basin basalts and E-type MORB, but are quite unlike the depleted island arc tholeiites. The diverse trace element and Sr isotope compositions of basalt-andesite from the back-arc depressions imply the interplay between E-type MORB and island arc tholeiite. These chemical characteristics and the relationships of (Ce/Yb)N vs (Ba/Ce)N and (Ce/Yb)N vs 87Sr/86Sr suggest that the back-arc depression magmas are generated by mixing of E-type MORB and depleted island arc tholeiite magmas. Geochemical characters of the associated rhyolite from the depression are compatible with partial melting of lower crust.  相似文献   

13.
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.  相似文献   

14.
87Sr/86Sr ratios of fourteen unaltered limestone and six fossil samples show a range of 0.7066-0.7118 for the depositional water of the Middle to Upper Pennsylvanian Madera Formation. The variation of these 87Sr/86Sr ratios may be due to the restricted depositional basin and nature of the source of the Madera Formation.While fossil and limestone samples are equally good for determination of strontium isotopic composition of depositional waters, leaches of calcareous shales contain significant amount of 87Sr leached from the noncarbonate fraction during acid treatment.  相似文献   

15.
首次在唐古拉地区晚二叠世—早三叠世拉卜查日组中获得牙形石化石,其分子为Hindeodus typicalis、H.eurypyge和H.praeparvus。根据其地层意义并结合层序地层学及海平面变化研究,最终将研究区二叠系与三叠系界线的可能位置定在实测剖面的29层顶、30层底。基于此,作者系统测试了拉卜查日组中的碳酸盐岩87Sr/86Sr比值,结果表明,二叠系/三叠系界线附近87Sr/86Sr比值为0.707017~0.707032,显著小于国内外其他地区二叠系/三叠系界线附近87Sr/86Sr比值。造成这种差异的主要原因,可能是由于唐古拉地区二叠系/三叠系界线附近存在广泛的火山活动以及上扬子地区二叠纪广泛的玄武岩喷发等地方性事件。此外,剖面上锶同位素演化曲线与海平面变化曲线对比显示,87Sr/86Sr比值的最小值与初始海泛面基本一致,锶同位素演化曲线与海平面变化曲线有着很好的一致性,说明全球海平面变化是其最主要的控制因素。  相似文献   

16.
The isotopic composition of strontium of pore water and of authigenic minerals leached from the sediment of core 119K with hot aqua regia is similar to that of the brine in the Discovery deep and differs from that of normal seawater. The average 87Sr86Sr ratio of strontium removed by acid leaching is 0.7077 ± 0.0007 (1σ) compared to a value of 0.70904 for the Red Sea. The detrital silicate fraction exhibits an approximate inverse correlation between 87Sr86Sr ratios and strontium concentrations which provides tentative support for a model in which the detrital silicate fraction of deep-sea sediment is considered to be a mixture of terrigenous dust of sialic composition enriched in radiogenic 87Sr and of volcanogenic material of basaltic composition and low 87Sr abundance. The 87Sr86Sr ratios of the shells of foraminifers and pteropods, expressed as δ 87Sr‰ relative to 0.70904 for seawater, decrease from ?0.23 ± 0.17‰ at 90 cm to ?0.82 ± 0.17‰ at 273 cm and remain constant at this value to a depth of 450 cm. The lowering of the δ 87Sr values is attributed both to the presence of aragonite overgrowths on pteropod shells and to possible isotope exchange with strontium in the connate fluid.  相似文献   

17.
Carbonate rocks and natural waters exhibit a wide range in the concentration and isotopic composition of strontium. This wide range and the quantifiable covariation of these parameters can provide diagnostic tools for understanding processes of fluid-rock interaction. Careful consideration of the uncertainties associated with trace element partitioning, sample heterogeneity and fluid-rock interaction mechanisms is required to advance the application of the trace element and isotope geochemistry of strontium to studies of diagenesis, goundwater evolution, ancient seawater chemistry and isotope stratigraphy. A principal uncertainty involved in the application of Sr concentration variations to carbonate systems is the large range of experimental and empirical results for trace element partitioning of Sr between mineral and solution. This variation may be a function of precipitation rate, mineral stoichiometry, crystal growth mechanism, fluid composition and temperature. Calcite and dolomite in ancient limestones commonly have significantly lower Sr concentrations (20–70 p.p.m.) than would be expected from published trace element distribution coefficient values and Sr/Ca ratios of most modern sedimentary pore waters. This discrepancy probably reflects the uncertainties associated with determining distribution coefficient values. As techniques improve for the analytical measurement and theoretical modelling of Sr concentration and isotopic variations, the petrological analysis of carbonate samples becomes increasingly important. The presence of even small percentages of non-carbonate phases with high Rb concentrations and high 87 Sr86 Sr values, such as clay minerals, can have significant effects on the measured 87 Sr/86 Sr values of carbonate rocks, due to the decay of 87Rb to 87 Sr. For example, a Permian marine limestone with 50 p.p.m. Sr and 1 p.p.m. Rb will have a present-day 87 Sr/86 Sr value that is >2 × 10?4 higher than its original value. This difference is an order of magnitude greater than the analytical uncertainty, and illustrates the importance of assessing the need for and accuracy of such corrections. A quantitative evaluation of the effects of water-rock interaction on Sr concentrations and isotope compositions in carbonates strengthens the application of these geochemical tracers. Geochemical modelling that combines the use of trace elements and isotopes can be used to distinguish between different mechanisms of water-rock interaction, including diffusive and advective transport of diagenetic constituents in meteoric pore fluids during the recrystallization of carbonate minerals. Quantitative modelling may also be used to construct diagnostic fluid-rock interaction trends that are independent of distribution coefficient values, and to distinguish between mixing of mineral end-members and fluid-rock interaction.  相似文献   

18.
The 87Sr/86Sr ratios of evaporitic carbonates and sulphates from Miocene sediment cored in the Mediterranean Sea show a depletion of 87Sr when compared to the isotopic composition of the Miocene contemporaneous marine strontium: 0.70803 versus 0.70936. The arrival into the evaporitic environment of strontium brought by continental waters can explain this difference. The variation of the 87Sr/86Sr ratios is, nevertheless, noticeable only when the influence of the continental waters is already well marked. This is proved when one compares the results obtained with strontium, to the results of isotopic analysis made on oxygen, carbon, sulphur and hydrogen taken from the same samples.  相似文献   

19.
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.  相似文献   

20.
We report Sr and Pb isotope analyses for an extensive suite of volcanic rocks from the N. Mariana arc together with Sr and Pb isotope analyses of sediments from the nearby Mariana and Nauru basins. In addition ten of the most recent volcanic samples were analysed for 10Be.The Sr isotope compositions cluster tightly around 87Sr86Sr = 0.7035 being slightly but significantly higher than the Pacific ocean floor basalts on either side of the arc and agreeing well with previous data. In contrast, the large number of new Pb isotopic data presented significantly extends the observed range of Pb isotope compositions for volcanic rocks from the Mariana arc to more radiogenic compositions. The concentrations of 10Be were very low (< 0.5 × 106 atom g?1).These new data require either that the Pb and Sr isotopic compositions of the Mariana sub-arc mantle be substantially different from those of the mantle source of ocean floor basalts on either side of the arc, or that the enrichment in radiogenic Pb and Sr relative to the values observed in Pacific ocean floor basalts be related to the subduction process. We prefer the latter hypothesis in which radiogenic Sr and Pb in ocean floor sediments are added to M.O.R.B. type mantle either by direct assimilation of the sediments in partial melts or, more probably, by transfer in a fluid phase into the zone of magma production. The low 10Be concentrations observed suggest the removal of at least the top few metres of sediment during subduction.  相似文献   

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