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1.
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.  相似文献   

2.
We report the results of a detailed study of dissolved Sr isotopes in the Solimões and Beni‐Madeira Rivers of the Amazon basin. This study developed data collected over 8 years indicating large spatial and temporal variations in dissolved Sr isotopes among the rivers of the Amazon basin. The large 87Sr/86Sr variations were found to be correlated with the geology of the source areas of the suspended sediments. The Beni‐Madeira River displays a high average 87Sr/86Sr ratio and large 87Sr/86Sr fluctuations during the hydrological cycle. This large average value and fluctuations were related to the presence of Precambrian rocks and Ordovician sediments in the source area of the suspended sediment of the river. In contrast, the Solimões River displays a narrow range of Sr isotope ratio variations and an average value close to 0.709. This river drains mostly Phanerozoic rocks of northern Peru and Ecuador that are characterized by low Sr isotope ratios. The isotopic fluctuations in the Beni‐Madeira River were observed to propagate downstream at least as far as Óbidos. This signal is characterized by an inverse relationship between the concentration of elemental Sr and its isotopic ratios. We further demonstrate that the Sr isotopic composition and content in the Beni‐Madeira River is controlled by suspended sediments derived from the Andes. Despite draining areas underlain by Precambrian rocks and having high 87Sr/86Sr ratios, such rivers as the Negro and Tapajós play a minor role in the total Sr budget of the Amazon basin. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

3.
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.  相似文献   

4.
The Sr isotopic systematics in the weathering profiles of biotite granite and granite porphyry in southern Jiangxi Province were investigated. The results showed that during the chemical weathering of granites, remarked fractionation occurred between Rb and Sr. During the early stages of chemical weathering of granites, the released Sr/Si and Sr/Ca ratios are larger than those of the parent rocks, and the leaching rate of Sr is higher than those of Si, Ca, K, Rb, etc. Dynamic variations in relative weathering rates of the main Sr-contributing minerals led to fluctuation with time in 87Sr/86Sr ratios of inherent and released Sr in the weathering crust of granite. Successive weathering of biotite, plagioclase and K-feldspar made 87Sr/86Sr ratios in the weathering residues show such a fluctuation trend as to decrease first, increase, and then decrease again till they maintain stable. This work further indicates that when Sr isotopes are used to trace biogeochemical processes on both the catchment and global scales, one must seriously take account of the prefer-ential release of Sr from dissolving solid phase and the fluctuation of 87Sr/86Sr ratios caused by the variations of relative weathering rates of Sr-contributing minerals.  相似文献   

5.
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.  相似文献   

6.
The Sr isotopic systematics in the weathering profiles of biotite granite and granite porphyry in southern Jiangxi Province were investigated. The results showed that during the chemical weathering of granites, remarked fractionation occurred between Rb and Sr. During the early stages of chemical weathering of granites, the released Sr/Si and Sr/Ca ratios are larger than those of the parent rocks, and the leaching rate of Sr is higher than those of Si, Ca, K, Rb, etc. Dynamic variations in relative weathering rates of the main Sr-contributing minerals led to fluctuation with time in87Sr/86Sr ratios of inherent and released Sr in the weathering crust of granite. Successive weathering of biotite, plagioclase and K-feldspar made87Sr/86Sr ratios in the weathering residues show such a fluctuation trend as to decrease first, increase, and then decrease again till they maintain stable. This work further indicates that when Sr isotopes are used to trace biogeochemical processes on both the catchment and global scales, one must seriously take account of the preferential release of Sr from dissolving solid phase and the fluctuation of87Sr/86Sr ratios caused by the variations of relative weathering rates of Sr-contributing minerals.  相似文献   

7.
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.  相似文献   

8.
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* = Nar? Clr) 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 (Srs) 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.  相似文献   

9.
Dissolved major ions, Sr concentrations and 87Sr/86Sr ratios of 10 coastal lakes from the Larsemann Hills, East Antarctica have been studied to constrain their solute sources, transport and glacial weathering patterns in their catchments. In absence of perennial river/streams, lakes serve as only reliable archive to study land surface processes in these low-temperature regions. The lake water chemistry is mostly Na-Cl type and it does not show any significant depth variations. Sr isotope compositions of these lakes vary from 0.7110 to 0.7211 with an average value of 0.7145, which is higher than modern seawater value. In addition to oceanic sources, major ions and Sr isotopic data show appreciable amount of solute supply from chemical weathering of silicate rocks in lake catchments and dissolution of Ca-Mg rich salts produced during the freezing of seawaters. The role of sulphide oxidation and carbonate weathering are found to be minimal on lake hydro-chemistry in this part of Antarctica. Inverse model calculations using this chemical dataset provide first-order estimates of dissolved cations and Sr; they are mostly derived from oceanic (seawater + snow) sources (cations approximately 76%) and (Sr approximately 92%) with minimal supplies from weathering of silicates (cations approximately 15%); (Sr approximately 2%) and Ca-rich minerals (cations approximately 9%); (Sr approximately 7%). The silicate weathering rate and its corresponding atmospheric CO2 consumption rate estimates for Scandrett lake catchment (3.6 ± 0.3 tons/km2/year and 0.5 × 105 moles/km2/year), are lower than that of reported values for the average global river basins (5.4 tons/km2/year and 0.9 × 105 tons/km2/year) respectively. The present study provides a comprehensive report of chemical weathering intensity and its role in atmospheric CO2 consumption in low-temperature pristine environment of Antarctica. These estimates underscore the importance of Antarctica weathering on atmospheric CO2 budget, particularly during the past warmer periods when the large area was exposed and available for intense chemical weathering.  相似文献   

10.
We have determined K, Rb and Sr concentrations and87Sr/86Sr ratios in fresh surface waters, a rain water sample and five geothermal waters from the Cantal volcanic area in the Massif Central, France. A comparison with appropriate rock types of the region showed no apparent chemical and isotopic fractionation occurring in the fresh water-surface rock system. The thermo-mineral water results suggest that all springs discharge dissolved Sr from the following contributors: Hercynian granito-metamorphic basement, lacustrian sediments underlying the volcano, Miocene-Pliocene volcanic rocks of basaltic to rhyolitic composition.  相似文献   

11.
The lavas produced by the Timanfaya eruption of 1730–1736 (Lanzarote, Canary Islands) contain a great many sedimentary and metamorphic (metasedimentary), and mafic and ultramafic plutonic xenoliths. Among the metamorphosed carbonate rocks (calc-silicate rocks [CSRs]) are monomineral rocks with forsterite or wollastonite, as well as rocks containing olivine ± orthopyroxene ± clinopyroxene ± plagioclase; their mineralogical compositions are identical to those of the mafic (gabbros) and ultramafic (dunite, wherlite and lherzolite) xenoliths. The 87Sr/86Sr (around 0.703) and 143Nd/144Nd (around 0.512) isotope ratios of the ultramafic and metasedimentary xenoliths are similar, while the 147Sm/144Nd ratios show crustal values (0.13–0.16) in the ultramafic xenoliths and mantle values (0.18–0.25) in some CSRs. The apparent isotopic anomaly of the metamorphic xenoliths can be explained in terms of the heat source (basaltic intrusion) inducing strong isotopic exchange (87Sr/86Sr and 143Nd/144Nd) between metasedimentary and basaltic rocks. Petrofabric analysis also showed a possible relationship between the ultramafic and metamorphic xenoliths.  相似文献   

12.
Tholeiitic basalts and sulfide deposits from the “Cyana” and “Alvin” diving programs (RITA project) on the East Pacific Rise were analyzed for Pb and Sr isotopes. The basalt data plot within the field defined previously by other East Pacific Rise basalts (206Pb/204Pb: 18.35–18.58;207Pb/204Pb: 15.48–15.53;208Pb/204Pb: 37.8–38.1;87Sr/86Sr: 0.7022–0.7025). Pb, U and Sr contents (～0.5, ～0.05 and ～110 ppm, respectively) and μ values (～6) are typical of MORB, whereas Th/U ratios (～3.5) are significantly higher.The Pb isotopic ratios of the sulfide samples are very homogeneous (206Pb/204Pb～18.47207Pb/204Pb～15.49208Pb/204Pb～37.90), and plot in the middle of the basalt field. This indicates that (1) the sulfide Pb was derived from the basaltic crust without any significant contribution from either seawater or hemipelagic sediments, and (2) the solutions from which the sulfides were deposited had uniform Pb isotopic composition. The Pb contents of three sulfide samples is relatively high (170–1310 ppm).The Sr contents of five sulfide samples are widely scattered from 12 to 210 ppm, with87Sr/86Sr ratios intermediate between basaltic and seawater values (0.70554±0.00005 to0.70795±0.00011). Leaching experiments show that both basalt-derived Sr and seawater Sr were present in the solutions which deposited the sulfides. In some cases, Sr was also adsorbed from seawater onto the sulfides following their deposition. Basalt-derived Sr and seawater Sr are also present in associated non-sulfide phases.  相似文献   

13.
Initial87Sr/86Sr ratios have been determined for 34 plutonic and volcanic rocks covering the entire age span of magmatic events associated with the Andean orogeny between latitudes 26° and 29° south. The igneous rocks, the majority dated by K/Ar mineral techniques, range in age from Lower Jurassic (190 m.y.) to Quaternary (0.89 m.y.). In addition, initial ratios were determined for three granitoid plutons and one metasediment from the pre-Mesozoic basement which underlies the entire Andean orogen in this transect at shallow depth. The compositions vary from basalt to rhyolite, and from quartz diorite to granodiorite or trondjemite, for the extrusives and intrusives, respectively.Mid-Cretaceous to Quaternary rocks exhibit a systematic west to east increase in mean strontium isotope ratio from 0.7022 to 0.7077, whereas the initial ratios of Jurassic plutons vary from 0.7043 to 0.7059, and do not correlate with age.The existence of unusually low initial ratios (e.g. 0.7022, 0.7023) for several Mesozoic plutonic rocks strongly implies a sub-crustal source for at least some of the Andean magmas. The time-dependent post-Jurassic increase in initial ratio is considered to reflect a systematic change in the composition of partial melts generated in response to the progressive subduction of a lithospheric slab. It is suggested that a systematic change in the locus of melting takes place from along or close to the upper surface of the subduction slab into hanging-wall mantle peridotite as subduction continues.  相似文献   

14.
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.  相似文献   

15.
Strontium isotope ratios and rare-earth element abundances have been measured in acid, intermediate and basic rocks from three late to postglacial volcanic complexes, and several other postglacial basalts in Iceland. Late and postglacial basalts in Iceland have been generated from a source region which is essentially homogeneous with respect to87Sr/86Sr. The mean87Sr/86Sr ratio for the basalts analysed is 0.70328 and the range is from 0.70317 ± 6to0.70334 ± 5 (2σ).Acid rocks from the Kerlinganfjöll and Namafjall volcanic complexes have87Sr/86Sr ratios which are indistinguishable from analysed basalts from the same complexes. However, intermediate and acid rocks from the Torfajökull complex have significantly higher87Sr/86Sr ratios and could not have been derived by fractional crystallization from basaltic magmas similar to those found in the same complex. These latter rocks have most probably been produced by remelting of Tertiary gabbroic rocks in Layer 3. Most of the basalts analysed have higher total rare-earth element abundances than typical dredged ocean-ridge tholeiites, and show less light rare-earth depletion. Intermediate and acid compositions show overall higher abundances and light rare-earth enrichments. The measured rare-earth abundances are compared with abundances generated by differential partial melting of various model source regions.It is shown that both the tholeiitic and alkali basalt compositions could be generated from the same source material by different degrees of partial melting. Variable partial melting of gabbroic material may account for the rare-earth element abundances of both the rhyolitic rocks (small degrees of melting) and the intermediate rocks (more extensive melting).  相似文献   

16.
Eighteen basic rocks from Ascension Island (South Atlantic) give a mean87Sr/86Sr ratio of 0.70311 ± 17 for both volcanics and plutonic inclusions. The late-stage differentiated rocks (rhyolites and granitic inclusions) have much higher87Sr/86Sr ratios, up to 0.712. All these rocks display the same range of Nd isotopic compositions (εNdvalues from6.9to11.1with a mean on12samples of8.4 ± 0.6) implying a cogenetic relation between the two sequences. The D/H systematics lead to the same conclusion.In the NdSr diagram, the data plot close to the mantle array and show a positive correlation. This suggests a mixing between a depleted MORB-type mantle, i.e. the upper mantle, and a hot-spot with less depleted geochemical characteristics, i.e. the OIB mantle source.The total range of δ18O values lies between 4.8‰ for plagioclase cumulates and 6.7‰ for the most evolved rocks (peralkaline granites and comendites). The basic rocks have values around 5.3‰, typical of mantle-derived material. These oxygen data indicate that the high87Sr/86Sr ratios in the most evolved rocks (both volcanic and plutonic terms) result from the combination of two different processes: incorporation of slight amounts (< 1%) of high-temperature altered oceanic crust by the magma in the late stages of the differentiation process and then in-situ Rb decay since the time of formation of these rocks. Both processes were very effective because of the high Rb and low Sr contents of these evolved rocks.Oxygen isotope systematics in the Ascension Island granites and rhyolites indicate that a fractional crystallization process alone does not produce δ18O values higher than 6.7‰, i.e. that the ultimate δ18O enrichment, relative to the initial basic magma, is not greater than 1.5‰.  相似文献   

17.
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.  相似文献   

18.
The Pampean Ranges of northwest Argentina are a basin-and-range tectonic province with a late Precambrian to Paleozoic basement and extensive Miocene-Recent calc-alkaline volcanism. The volcanoes include the large resurgent Cerro Galan caldera, and Recent scoria cones and lava flows. Miocene-Recent volcanic rocks of basalt to dacite composition from the Cerro Galan area exhibit a range of Rb/Sr ratios of 0.043–1.092 and initial87Sr/86Sr ratios of 0.7057–0.7115 with a clear positive correlation between87Sr/86Sr and87Rb/86Sr, indicating an apparent age of ca. 130 Ma. This relationship is interpreted to indicate that the Sr isotope variation in the Cerro Galan volcanic rocks results from mixing of a mantle-derived component with low87Sr/86Sr (<0.7057) and high Sr (>700 ppm) with a crustal component characterized by higher87Sr/86Sr (>0.7115) and lower Sr (<240 ppm). It is concluded that the mixing is best explained as a result of a small degree of selective crustal Sr contamination (ca. 10%) of a range of subsequently erupted magmas produced largely by fractional crystallization within the continental crust. We propose that the mantle-derived end-member is derived by partial melting of sub-Andean mantle with an87Sr/86Sr ratio of ca. 0.704, and that such an Sr isotope ratio characterizes the source region for calc-alkaline volcanic rocks throughout the Andes.  相似文献   

19.
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.  相似文献   

20.
To evaluate influence of chemical weathering of the Qinghai-Tibet Plateau (QTP) on seawater 87Sr/86Sr variation, river water and sediment samples were collected, and their Sr concentrations and isotopic compositions analyzed, from the seven large rivers that originated from the QTP. By combining these with the data of the Ganges, Brahmaputra, Indus and Irrawaddy originated in the southern QTP, the total Sr flux of the eleven rivers reaches 3.47×109 mol·a−1, which accounts for 10.2% of the total Sr flux transported by the global rivers. The weighted mean 87Sr/86Sr is 0.71694, higher than the average value of the global rivers. The 87Srex (87Sr flux in excess of the seawater 87Sr/86Sr ratio) of the Chinese seven rivers is 1.55×106 mol·a−1, only accounting for about 6% of the value of the eleven rivers originated from QTP, and the Ganges-Brahmaputra system accounts for 86%. We assume that the QTP rivers have no strontium contributions to the oceans before ∼40 Ma and the Sr fluxes of the global rivers, except the QTP eleven rivers, are constant, then a maximum linear increase in Sr fluxes of the QTP rivers from zero to the modern value in response to tectonic uplift can explain ∼69% increase of seawater 87Sr/86Sr over the past ∼40 Ma and the remainder of 31% is perhaps provided from other factors. Supported by National Natural Science Foundation of China (Grant Nos. 40473009, 40331001, 40873001)  相似文献   

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