首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 22 毫秒
1.
A numerical model for the diagenetic exchange of Sr between carbonates and their pore fluids during sedimentation and compaction has been developed. The model has been applied to data from DSDP Site 590B in order to assess the accuracy with which the Sr isotope record in the carbonate sediment reflects that of seawater. The most important process affecting the Sr in the solid carbonate is exchange with the pore fluid due to solution-reprecipitation, but the concentration or isotopic composition of Sr in the solid itself gives little or no information as to the magnitude of this exchange. The key to determining the rate of exchange is the pore fluid, where the variations of Sr2+ and87Sr/86Sr with depth are very sensitive indicators. The logical structure of applying the model to data from DSDP 590B is to find by successive iteration an ocean history (i.e., the initial87Sr/86Sr and Sr concentration of each increment of carbonate deposited) and a rate of Sr exchange between pore water and solid carbonate such that the model matches the present Sr concentration and87Sr/86Sr of both pore water and solid carbonate.Once all the data are matched, the model provides an estimate of the rate of Sr exchange due to solution-reprecipitation and the evolution of87Sr/86Sr in seawater over the past 20 million years. For DSDP 590B we find that solution-reprecipitation decreases rapidly with depth, from a near surface value of about 10% per million years to about 1% per million years below 200 m. This rate of exchange of Sr results in the carbonates of DSDP 590B preserving an accurate record of the Sr isotopic evolution of the ocean over the past 5 million years, but for ages greater than 5 million years the87Sr/86Sr ratio of the carbonate is systematically displaced from that of the seawater in which it was deposited. The maximum difference is of order 5 × 10−5.  相似文献   

2.
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   

3.
The87Sr/86Sr ratio of seawater strontium (0.7091) is less than the87Sr/86Sr ratio of dissolved strontium delivered to the oceans by continental run-off (～0.716). Isotope exchange with strontium isotopically lighter oceanic crust during hydrothermal convection within spreading oceanic ridges can explain this observation. In quantitative terms, the current87Sr/86Sr ratio of seawater (0.7091) may be maintained by balancing the continental run-off flux of strontium (0.59 × 1012 g/yr) against a hydrothermal recirculation flux of 3.6 × 1012 g/yr, during which the87Sr/86Sr ratio of seawater drops by 0.0011. A concomitant mean increase in the87Sr/86Sr ratio of the upper 4.5 km of oceanic crust of 0.0010 (0.7029–0.7039) should be produced. This required87Sr enrichment has been observed in hydrothermally metamorphosed ophiolitic rocks from the Troodos Massif, Cyprus.The post-Upper Cretaceous increase in the strontium isotopic composition of seawater(～0.7075–0.7091) covaries smoothly with inferred increase in land area. This suggests that during this period the main factor which has caused variability in the87Sr/86Sr ratio of seawater strontium could have been variation in the magnitude of the continental run-off flux caused by variation in land area. Variations in land area may themselves have been partly a consequence of variations in global mean sea-floor spreading rate.  相似文献   

4.
Measurements of 87Sr/86Sr ratios of interstitial waters from leg 25, site 245 and leg 38, site 336 of the Deep Sea Drilling Project show that the enrichment of Sr2+ with depth is caused both by the alteration of volcanic material and by the introduction of strontium derived from calcium carbonate. 87Sr/86Sr ratios range from 0.70913 to 0.70794 at site 245 and from 0.70916 to 0.70694 at site 336. The low ratios compared with contemporaneous seawater reflect the release of Sr from a volcanic source having, according to material-balance calculations, a 87Sr/86Sr ratio of about 0.7034 at site 336. At this site the source appears to be volcanic ash and not basaltic basement which acts as a sink for Sr2+ during in situ low-temperature weathering. The volcanic contribution to the strontium enrichment in the basal interstitial waters varies from <10% at site 245 to >50% at site 336. The remaining Sr2+ is derived from Sr-rich biogenic carbonate during diagenetic recrystallization to form Sr-poor calcite.  相似文献   

5.
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   

6.
To investigate the source, flow paths, and chemistry of rich resources of high‐quality, shallow groundwater in the alluvial fan between the Tedori and Sai rivers in central Japan, we analysed stable isotope ratios of H, O, and Sr and concentrations of major dissolved ions and trace elements in groundwater, river water, and paddy water. The 87Sr/86Sr ratios of the groundwater are related to near‐surface geology: groundwater in sediment from the Tedori River has high 87Sr/86Sr ratios (>0.711), whereas that from the Sai River in the north of the fan has low 87Sr/86Sr ratios (<0.711). δ2H and δ18O values and 87Sr/86Sr ratios indicate that groundwater in the central and southern fans is recharged by the Tedori River, whereas recharge in the north is from the Sai River. Mg2+, Ca2+, Sr2+, HCO3?, and SO42? concentrations and δ2H and δ18O values in the groundwater are high in the central fan and, except for the northern area, tend to increase with distance from the Tedori River. There are linear relationships between 87Sr/86Sr ratio and the reciprocal concentrations of Sr2+, Mg2+, and Ca2+. These geochemical characteristics suggest that as groundwater recharged from the Tedori River flows towards the central fan, it mixes with waters derived from precipitation and paddy water that have become enriched in these components during downward infiltration. These results are consistent with our hydrological analysis and numerical simulation of groundwater flow, thus verifying the validity of the model we used in our simulation of groundwater flow. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

7.
In the Samail ophiolite,147Sm-143Nd,87Rb-87Sr, and18O/16O isotopic systems have been used to distinguish between sea-floor hydrothermal alteration and primary magmatic isotopic variations. The Rb-Sr and18O/16O isotopic systems clearly exhibit sensitivity to hydrothermal interactions with seawater while the Sm-Nd system appears essentially undisturbed. Internal isochrons have been determined by the147Sm-143Nd method using coexisting plagioclase and pyroxene and give crystallization ages of 130 ± 12m.y. from Ibra and 100 ± 20 m.y. from Wadi Fizh. These ages are interpreted as the time of formation of the Samail oceanic crust and are older than the inferred emplacement age of 65–85 m.y. The initial143Nd/144Nd ratios for a tectonized harzburgite, cumulate gabbros, plagiogranite, sheeted dikes and a basalt have a limited range in εNd of from 7.5 to 8.6 for all lithologies, demonstrating a clear oceanic affinity and supporting earlier interpretations based on geologic observations and geochemistry. The87Sr/86Sr initial ratios on the same rocks have an extremely large range of from 0.70296 to 0.70650 (εSr = ?19.7 to +30.5) and the δ18O values vary from 2.6 to 12.7. These large variations are clearly consistent with hydrothermal interaction of seawater with the oceanic crust. A model is presented for the closed system exchange of Sr and O, that in principle illustrates how the Sr isotopic data may be utilized to estimate the water/rock ratio and subsequently used to evaluate the temperature of equilibration between the water and silicates from the18O/16O water-rock fractionation.  相似文献   

8.
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   

9.
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   

10.
Neodymium isotopic analyses have been measured on nine ophiolites and four orogenic lherzolites. εNd varies from +12 to +3 in the ophiolites and from +18 to +2 in the orogenic lherzolites. The majority of the analyses plot on a εNd-εSr correlation line as defined by Nd and Sr isotopic analyses of oceanic basalts. However, certain ophiolitic and lherzolitic samples exhibit high87Sr/86Sr ratios and as such lie to the right of the correlation line towards seawater compositions.From these data one can postulate several origins for ophiolites including that of mid-ocean ridges and ocean islands. If the orogenic lherzolites are interpreted as representative of the mantle occurring below active ridges a more complex model is required involving mantle heterogeneity and multi-episodic chemical fractionation starting prior to 2 Ga ago.  相似文献   

11.
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.  相似文献   

12.
Nd isotopic characteristics of S- and I-type granites   总被引：1，自引：0，他引：1  
The initial Nd and Sr isotopic composition has been determined in S- and I-type granites from the Paleozoic Berridale and Kosciusko Batholiths of southeast Australia. The Nd and Sr isotopic variations form a strongly covariant array with S-types granites having a relatively restricted range inεNd values from ?6.1 to ?9.8 but a large range in initial87Sr86Sr of from 0.7094 to 0.7184. These characteristics are indicative of an～1400-m.y. sedimentary or metasedimentary source for S-types. I-types have variable initial Nd ranging from +0.4 to ?8.9, and a more limited range in initial87Sr86Sr of from 0.70453 to 0.7119. These isotopic characteristics are consistent with a two-component mixing model whereby a depleted mantle-like component (DMC) withεNd = +6 and87Sr86Sr= 0.703, is mixed with a crustal component (CC) havingεNd = ?9 and87Sr86Sr= 0.720. Although this two-component mixing model satisfies the isotopic constraints the source rock chemistry of the I-types is not compatible with the large proportion (up to 50%) of sedimentary material implied by the isotopic data. This indicates that more than two components are required to account for both the isotopic and chemical data. Both the chemical and isotopic data are consistent with I-type granites having been formed from source rocks of predominantly mantle derivation and obtained progressively from the mantle over a period of 1000 m.y. prior to granite formation.  相似文献   

13.
δ87Sr values and Ca/Sr ratios were employed to quantify solute inputs from atmospheric and lithogenic sources to a catchment in NW Germany. The aquifer consists primarily of unconsolidated Pleistocene eolian and fluviatile deposits predominated by >90% quartz sand. Accessory minerals include feldspar, glauconite, and mica, as well as disperse calcium carbonate in deeper levels. Decalcification of near-surface sediment induces groundwater pH values up to 4.4 that lead to enhanced silicate weathering. Consequently, low mineralized Ca–Na–Cl- and Ca–Cl-groundwater types are common in shallow depths, while in deeper located calcareous sediment Ca–HCO3-type groundwater prevails. δ87Sr values and Ca/Sr ratios of the dissolved pool range from 7.3 to −2.6 and 88 to 493, respectively. Positive δ87Sr values and low Ca/Sr ratios indicate enhanced feldspar dissolution in shallow depths of less than 20 m below soil surface (BSS), while equilibrium with calcite governs negative δ87Sr values and elevated Ca/Sr ratios in deep groundwater (>30 m BSS). Both positive and negative δ87Sr values are evolved in intermediate depths (20–30 m BSS). For groundwater that is undersaturated with respect to calcite, atmospheric supplies range from 4% to 20%, while feldspar-weathering accounts for 8–26% and calcium carbonate for 62–90% of dissolved Sr2+. In contrast, more than 95% of Sr2+ is derived by calcium carbonate and less than 5% by feldspar dissolution in Ca–HCO3-type groundwater. The surprisingly high content of carbonate-derived Sr2+ in groundwater of the decalcified portion of the aquifer may account for considerable contributions from Ca-containing fertilizers. Complementary tritium analyses show that equilibrium with calcite is restricted to old groundwater sources.  相似文献   

14.
Neodymium isotope and REE analyses of recent volcanic rocks and spinel lherzolite nodules from the Afar area are reported. The143Nd/144Nd ratios of the volcanic rocks range from 0.51286 to 0.51304, similar to the range recorded from Iceland. However, the87Sr/86Sr ratios display a distinctly greater range (0.70328–0.70410) than those reported from the primitive rocks of Iceland. Whole rock samples and mineral separates from the spinel lherzolite nodules exhibit uniform143Nd/144Nd ratios (ca. 0.5129) but varied87Sr/86Sr ratios in the range 0.70427–0.70528.The SrNd isotope variations suggest that the volcanic rocks may have been produced by mixing between two reservoirs with distinct isotopic compositions. Two possible magma reservoirs in this area are the source which produced the “MORB-type” volcanics in the Red Sea and Gulf of Aden and the anomalous source represented by the nodule suite. The isotopic composition of the volcanics is compatible with mixing between these two reservoirs.It is shown that the anomalous source with a high87Sr/86Sr ratio cannot have been produced by simple processes of partial melting and mixing within normal mantle. Instead the high87Sr/86Sr is equated with a fluid phase. A primitive cognate fluid, subducted seawater or altered oceanic lithosphere may have been responsible for the generation of the source with a high87Sr/86Sr ratio.  相似文献   

15.
The primary isotopic characteristics of alkaline granites are often obscured by secondary processes enhanced by their unusual chemical compositions. This is true for radiogenic as well as for stable isotopes. For example, the 87Sr/86Sr ratios can vary drastically in closed systems because of very high Rb/Sr ratios and can also be easily modified by direct or indirect interaction with continental crust because of low Sr concentrations. Moreover, the frequent occurrence of the granitic massifs as hypovolcanic complexes increases the probability of interaction with meteoric waters which is a common source of important isotopic variability.The investigation of oxygen isotope systematics in alkaline acidic rocks from various environments shows the18O content of their quartz to be highly invariable, and the δ18O values to be close to the mantle range of values. This is due to the resistance of quartz to isotopic exchange, which makes it a good tracer of primary isotopic composition. If we eliminate the quartz δ18O values for which interaction with meteoric water is well documented (five samples), the total range of variation (seventeen samples) is from 6.0 to 7.3‰ relative to SMOW. The values can easily be accounted for by, and correspond to, equilibrium with mantle-type material in a temperature range of 1200-800°C. If we consider possible effects of fractional crystallization, this temperature range can probably be reduced to its lower limit which is much more likely for rocks of acidic composition.The present oxygen isotope study strongly supports an origin for alkaline anorogenic granites from mantle-dominated sources.  相似文献   

16.
Strontium, neodymium isotopic compositions and trace elements of the detrital sediments of Core NS90-103 from South China Sea were analyzed. The results show that the87Sr/86Sr ratios of the detritus during the last glacial range from 0.722 4 to 0.723 0. They are significantly higher than those during the Holocene and the maximum of the last interglacial, which range from 0.721 0 to 0.721 7. This indicates stronger continental weathering during the last glacial. On the other hand, the143Nd/144Nd ratios of these detritus are higher during the last glacial too, similar to the variation of the87Sr/86Sr ratios. The trace element geochemistry of these detritus indicates that more authigenic sediments, such as ferromanganese, during the last glacial may partly contribute to the increase of143Nd/144Nd ratios. Furthermore, much more detritus from continent of South China to the north of the South China Sea may probably contribute to143Nd/144Nd ratios increase during the last glacial, which was the result of the enhancement of northeast monsoon.  相似文献   

17.
Sr isotope geochemical studies (the 87Sr/86Sr and ?18O-87Sr/86Sr systems) on the wall rocks and ores from the Lemachang independent Ag deposit in northeastern Yunnan provide strong evidence that the ore-forming fluids had flown through radiogenetically Sr-enriched rocks or strata prior to their entry into the locus of ore precipitation, and water-rock interaction is the main mechanism of Ag ore precipitation. The radiogenetically Sr-enriched source region may be the Proterozoic basement (the Kunyang and Hekou groups). Moreover, the theoretical modeling of the Sr isotopic system indicates that the ore-forming fluids contain as much as 3×10?6 Sr with isotopic composition of Sr being 0.750 and that of oxygen 7.0‰. The ore-forming temperatures were estimated at 150-250℃ for the carbonate rock-type ores and at 200-260℃ for the clastic rock-type.  相似文献   

18.
陈晨  金章东  徐阳  李良波  苟龙飞  张飞 《湖泊科学》2020,32(6):1882-1890
2008年5月12日里氏7.9级汶川大地震引发了超过56000多个山体滑坡，在龙门山地区产生巨量的碎屑物质，极大地影响了流域的地表过程.然而，地震对河流碎屑物质组成及沉积过程的改变却知之甚少.紫坪铺水库超高沉积速率（平均74 cm/a）的沉积物完整记录了汶川地震前后的沉积过程，为研究2008年汶川地震对流域地表物质搬运及沉积物组成的影响提供了宝贵的素材.本研究测试了汶川地震前后紫坪铺水库沉积物的Sr同位素以及元素组成，结果表明其在地震之后均发生了显著变化.震后沉积物87Sr/86Sr与Rb/Sr比值同步降低，并且和沉积物化学蚀变指数（CIA）呈正相关性，反映了地震滑坡导致的新鲜物质对沉积物的贡献，特别是地震后强径流的2010—2011年.地震前后沉积物组成的差异性，为利用沉积物反演水文气候和构造事件及其环境效应提供了基础和潜在指标.  相似文献   

19.
New data for the direct measurement of the isotopic composition of neodymium in Atlantic Ocean seawater are compared with previous measurements of Pacific Ocean seawater and ferromanganese sediments from major ocean basins. Data for Atlantic seawater are in excellent agreement with Nd isotopic measurements made on Atlantic ferromanganese sediments and are distinctly different from the observed compositions of Pacific samples. These results clearly demonstrate the existence of distinctive differences in the isotopic composition of Nd in the waters of the major ocean basins and are characteristic of the ocean basin sampled. The average εNd(0) values for the major oceans as determined by data from seawater and ferromanganese sediments are as follows: Atlantic Ocean,εNd(0) ? ?12 ± 2; Indian Ocean,εNd(0) ? ?8 ± 2; Pacific Ocean,εNd(0) ? ?3 ± 2. These values are considerably less than εNd(0) value sources with oceanic mantle affinities indicating that the REE in the oceans are dominated by continental sources. The difference in the absolute abundance of143Nd between the Pacific and Atlantic Oceans corresponds to ～106 atoms143Nd per gram of seawater. The correspondence between the143Nd/144Nd in seawater and in the associated sediments suggests the possible application of this approach to paleo-oceanography.Distinctive differences in εNd(0) values are observed in the Atlantic Ocean between deep-ocean water associated with North Atlantic Deep Water and near-surface water. This suggests that North Atlantic Deep Water may be relatively well mixed with respect to Nd isotopic composition whereas near-surface water may be quite heterogeneous, reflecting different sources for surface waters relative to deep water. This suggests that it may be possible to distinguish the sources of water masses within an ocean basin on the basis of Nd isotopic composition.The Nd isotopic variations in seawater are used to relate the residence time of Nd and mixing rates between the oceans.  相似文献   

20.
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   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号