Rare earth element and strontium isotope geochemistry in Dujiali Lake,central Qinghai-Tibet Plateau,China: Implications for the origin of hydromagnesite deposits

Rare earth element (REE) and strontium isotope data (⁸⁷Sr/⁸⁶Sr) are presented for hydromagnesite and surface waters that were collected from Dujiali Lake in central Qinghai-Tibet Plateau (QTP), China. The goal of this study is to constrain the solute sources of hydromagnesite deposits in Dujiali Lake. All lake waters from the area exhibit a slight LREE enrichment (average [La/Sm]_PAAS = 1.36), clear Eu anomalies (average [Eu/Eu*]_PAAS = 1.31), and nearly no Ce anomalies. The recharge waters show a flat pattern (average [La/Sm]_PAAS = 1.007), clear Eu anomalies (average [Eu/Eu*] _PAAS = 1.83), and nearly no Ce anomalies (average [Ce/Ce*]_PAAS = 1.016). The REE+Y data of the surface waters indicate the dissolution of ultramafic rock at depth and change in the hydrogeochemical characteristics through fluid-rock interaction. These data also indicate a significant contribution of paleo-groundwater to the formation of hydromagnesite, which most likely acquired REE and Sr signatures from the interaction with ultramafic rocks. The ⁸⁷Sr/⁸⁶Sr data provide additional insight into the geochemical evolution of waters of the Dujiali Lake indicating that the source of Sr in the hydromagnesite does not directly derive from surface water and may have been influenced by both Mg-rich hydrothermal fluids and meteoric water. Additionally, speciation modeling predicts that carbonate complexes are the most abundant dissolved REE species in surface water. This study provides new insights into the origins of hydromagnesite deposits in Dujiali Lake, and contributes to the understanding of hydromagnesite formation in similar modern and ancient environments on Earth.     

Mineralogy and geochemistry of the Holocene lacustrine sediments in Nam Co, Tibet

The carbonates, clays and major chemical compositions of lacustrine sediments in Nam Co (Lake) were examined by X-ray diffraction, scanning electron microscopy and chemical analysis. Carbonates include monohydrocalcite (MHC, first report from China and in a high-altitude lake), low-Mg calcite and traces of dolomite. MHC in Nam Co is developed in water (1.8 g/L) with high Mg/Ca molar ratios (10.03–15.03), high pH (8.04–9.72) and the presence of bacteria, algae, diatom and ostracoda. Illite and Mg-chlorite provide a strong evidence for physical weathering in the Holocene. Most Ca and Sr in sediments originate from carbonates as the molar ratios of Ca and CO₃²⁻ are all less than 1 and the curve of Sr is very similar to that of Ca. However, most of the Mg, Fe and Rb are from clays. The lake water shifted from a fresh water environment to an evaporative, alkaline environment by 2.06 cal. ka BP. There was a depositional event that the depositional rate changed from 0.134 to 1.639 mm/a at about 2 cal. ka BP.     

Constraints from strontium and neodymium isotopic ratios and trace elements on the sources of the sediments in Lake Huguang Maar

The sediments in Lake Huguang Maar in coastal South China were previously thought to originate mainly from wind-blown dust transported from North China, such that the lake sediments recorded the varying strength of the Asian winter monsoon. An alternative explanation was that the local pyroclastic rocks supplied the lake sediments, but the actual contributions from the different sources remained unclear. Geochemical analyses including ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd and trace elements support the local pyroclastic rock as the dominant source: < 22% of the total Sr in the lake sediments and  17% of the Nd arises from the distant source. Nb/Ta and Zr/Hf for the lake sediments are identical to those for the local rock but differ from the ratios for the wind-blown dust, and chondrite-normalized rare earth element patterns for the lake sediments are similar to those for the local rock and soil, but differ from those for the distant source. The sediments in Lake Huguang Maar are probably input into the lake through runoff and thus controlled by the hydrology of the lake. Wind-blown dust transported by the Asian winter monsoon from arid North China is only a minor contribution to the sediments.     

Ra and Th adsorption coefficients in lakes—Lake Kinneret (Sea of Galilee) “natural experiment”

The adsorption rate constants of Ra and Th were estimated from empirical data from a freshwater lake and its feeding saline springs. We utilized the unique setting of Lake Kinneret (Sea of Galilee, northern Israel) in which most of the Ra and Th nuclides are introduced into the lake by saline springs with high ²²⁶Ra activities and a high ²²⁴Ra/²²⁸Ra ratio of 1.5. The mixing of the Ra enriched saline waters and freshwater in the lake causes the ²²⁴Ra/²²⁸Ra ratio to drop down to 0.1 in the Kinneret due to preferential adsorption of ²²⁸Th. These conditions constitute a “natural experiment” for estimating adsorption rates. We developed a simple mass-balance model for the radionuclides in Lake Kinneret that accurately predicted the Ra isotope ratios and the ²²⁶Ra activity in the lake. The model is comprised of simultaneous equations; one for each radionuclide. The equations have one input term: supply of radionuclides from the saline springs; and three output terms: adsorption on particles in the lake, radioactive decay and outflow from the lake. The redundancy in the analytical solutions to the mass balance equations for the relevant nuclides constrained the values of Ra and Th adsorption rate constants to a very narrow range. Our results indicate that the adsorption rate constant for Ra is between 0.005 d⁻¹ and 0.02 d⁻¹. The rate constant for Th is between 0.5 d⁻¹ and 1 d⁻¹, about fifty to a hundred times higher. The estimated desorption rate coefficient for Ra is about 50-100 times larger than its adsorption rate constant. The mass-balance equations show that the residence times of all Ra isotopes (²²⁶Ra, ²²⁸Ra,²²³Ra, ²²⁴Ra) and of ²²⁸Th in the lake are about 95, 92, 14, 6 and 1 d, respectively. These residence times are much shorter than the residence time of water in the lake (about 5.5 y). The steady state activity ratios in Lake Kinneret depend mainly on the adsorption rate constants, decay constants, the outflow rate from the lake and the activity ratios in the saline springs. The activity ratios are independent of the saline springs flow rate.     

Constraints on water chemistry by chemical weathering in the Lake Qinghai catchment, northeastern Tibetan Plateau (China): clues from Sr and its isotopic geochemistry

Lake water, river water, and groundwater from the Lake Qinghai catchment in the northeastern Tibetan Plateau, China have been analyzed and the results demonstrate that the chemical components and ⁸⁷Sr/⁸⁶Sr ratios of the waters are strictly constrained by the age and rock types of the tributaries, especially for groundwater. Dissolved ions in the Lake Qinghai catchment are derived from carbonate weathering and part from silicate sources. The chemistry of Buha River water, the largest tributary within the catchment, underlain by the late Paleozoic marine limestone and sandstones, constrains carbonate-dominated compositions of the lake water, being buffered by the waters from the other tributaries and probably by groundwater. The variation of ⁸⁷Sr/⁸⁶Sr ratios with cation concentrations places constraint on the Sr-isotopic compositions of the main subcatchments surrounding Lake Qinghai. The relative significance of river-water sources from different tributaries (possibly groundwater as well) in controlling the Sr distribution in Lake Qinghai provides the potential to link the influence of hydrological processes to past biological and physical parameters in the lake. The potential role of groundwater input in the water budget and chemistry of the lake emphasizes the need to further understand hydrogeological processes within the Lake Qinghai system.     

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.     

The late Quaternary limnological history of Lake Kinneret (Sea of Galilee), Israel

The freshwater Lake Kinneret (Sea of Galilee) and the hypersaline Dead Sea are remnant lakes, evolved from ancient water bodies that filled the tectonic depressions along the Dead Sea Transform (DST) during the Neogene-Quartenary periods. We reconstructed the limnological history (level and composition) of Lake Kinneret during the past ∼40,000 years and compared it with the history of the contemporaneous Lake Lisan from the aspect of the regional and global climate history. The lake level reconstruction was achieved through a chronological and sedimentological investigation of exposed sedimentary sections in the Kinnarot basin trenches and cores drilled at the Ohalo II archeological site. Shoreline chronology was established by radiocarbon dating of organic remains and of Melanopsis shells.The major changes in Lake Kinneret level were synchronous with those of the southern Lake Lisan. Both lakes dropped significantly ∼42,000, ∼30,000, 23,800, and 13,000 yr ago and rose ∼39,000, 26,000, 5000, and 1600 yr ago. Between 26,000 and 24,000 yr ago, the lakes merged into a unified water body and lake level achieved its maximum stand of ∼170 m below mean sea level (m bsl). Nevertheless, the fresh and saline water properties of Lake Kinneret and Lake Lisan, respectively, have been preserved throughout the 40,000 years studied. Calcium carbonate was always deposited as calcite in Lake Kinneret and as aragonite in Lake Lisan-Dead Sea, indicating that the Dead Sea brine (which supports aragonite production) never reached or affected Lake Kinneret, even during the period of lake high stand and convergence. The synchronous level fluctuation of lakes Kinneret, Lisan, and the Holocene Dead Sea is consistent with the dominance of the Atlantic-Mediterranean rain system on the catchment of the basin and the regional hydrology. The major drops in Lake Kinneret-Lisan levels coincide with the timing of cold spells in the North Atlantic that caused a shut down of rains in the East Mediterranean and the lakes drainage area.     

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.     

Strontium isotope composition of alpine-type ultramafic rocks in the Lake Chatuge District,Georgia—North Carolina

The ⁸⁷Sr/⁸⁶Sr ratios for a series of ultramafic rocks from the Lake Chatuge region range from 0.7023 to 0.7047, suggesting a direct upper mantle source and precluding a multiple differentiation origin for these alpine-type rocks. Higher ⁸⁷Sr/⁸⁶Sr ratios (0.7058–0.7068) for serpentinized rocks from this suite apparently reflect the influx of radiogenic ⁸⁷Sr from the surrounding gneisses and schists during serpentinization.     

Environmental Evolution of the Water Body of Qinghai Lake since the Postglacial Age

Based on the data developed from various s natural waters in the Qinghai Lake area and ostracode shells present in drill core QH-16A of recent lake-floor sediments ,this paper discusses the distribution of stable isotopes in the modern water body of Qinghai Lake,and the initial isotopic composition of the lake water has been deduced ,Studies of δ^18O,δ^13C,Mg/Ca and Sr/Ca in ostracode shells provide the basis for the establishment of the model of climatic fluctuation in the Qinghai Lake area since the postaglacial age,as well as for the elucidation of the environmental evolution of the water body of Qinghai Lake since the postglacial age.     

Strontium Isotopic Signatures of the Streams and Lakes of Taylor Valley, Southern Victoria Land, Antarctica: Chemical Weathering in a Polar Climate

We have collected and analyzed a series of water samples from three closed-basin lakes (Lakes Bonney, Fryxell, and Hoare) in Taylor Valley, Antarctica, and the streams that flow into them. In all three lakes, the hypolimnetic waters have different ⁸⁷Sr/⁸⁶Sr ratios than the surface waters, with the deep water of Lakes Fryxell and Hoare being less radiogenic than the surface waters. The opposite occurs in Lake Bonney. The Lake Fryxell isotopic ratios are lower than modern-day ocean water and most of the whole-rock ratios of the surrounding geologic materials. A conceivable source of Sr to the system could be either the Cenozoic volcanic rocks that make up a small portion of the till deposited in the valley during the Last Glacial Maximum or from marble derived from the local basement rocks. The more radiogenic ratios from Lake Bonney originate from ancient salt deposits that flow into the lake from Taylor Glacier and the weathering of minerals with more radiogenic Sr isotopic ratios within the tills. The Sr isotopic data from the streams and lakes of Taylor Valley strongly support the notion documented by previous investigators that chemical weathering has been, and is currently, a major process in determining the overall aquatic chemistry of these lakes in this polar desert environment.     

Spatial and temporal variations of Rb/Sr ratios of the bulk surface sediments in Lake Qinghai

The Rb/Sr ratios of lake sediments have been suggested as indicators of weathering intensity by increasing work. However, the geochemistry of Rb/Sr ratios of lake sediments is variable between different lakes. In this study, we investigated the spatial and temporal patterns of Rb/Sr ratios, as well as those of other major elements in surface sediments of Lake Qinghai. We find that the spatial pattern of Rb/Sr ratios of the bulk sediments correlates well with that of the mass accumulation rate, and those of the terrigenous fractions, e.g., SiO₂, Ti, and Fe. The temporal variations of Rb/Sr ratios also synchronize with those of SiO₂, Ti, and Fe of each individual core. These suggest that Rb/Sr ratios of the surface sediments are closely related to terrigenous input from the catchment. Two out of eight cores show similar trends between Rb/Sr ratios and precipitation indices on decadal scales; however, the other cores do not show such relationship. The result of this study suggests that physical weathering and chemical weathering in Lake Qinghai catchment have opposite influence on Rb/Sr ratios of the bulk sediments, and they compete in dominating the Rb/Sr ratios of lake sediments on different spatial and temporal scales. Therefore, it is necessary to study the geochemistry of Rb/Sr ratio of lake sediments (especially that on short term timescales) particularly before it is used as an indicator of weathering intensity of the catchment.     

The new data on the origin of the Patom Crater (East Siberia)

It has been found that the origin of the Patom Crater is related to endogenous processes with the main role played by deep flow of fluid components, which determine formation of the ejecta cone at about 500 years ago or more. This is evidenced by the zonal structure of the crater and geochemical peculiarities of rocks, caused by the long formation time for particular zones. Sandstone and schist blocks that were included into eruptive breccia within the crater were affected by gaseous or fluid components and intensively carbonized. During carbonatization, these rocks within the crater were being enriched in Ca and Sr, but the shares of the ⁸⁷Sr and, consequently, ⁸⁷Sr/⁸⁶Sr ratio in them abruptly decrease. This is explained by the influence of deep fluids on terrigenous rocks, which were initially depleted in the radiogenic strontium isotope and might flow from a magmatic source with a low ⁸⁷Sr/⁸⁶Sr ratio. However, these fluids were enriched in CO2 and transported significant quantities of Sr, which led to enrichment of all terrigenous rocks in the crater in this element. The discovery of individual sandstone blocks with high concentrations of summarized rare earth elements (up to 557 g/t) and higher Sr and Ba contents among the fragments of host stratum within the Patom Crater allows us to suppose that there is a magmatic source enriched in fluid components at depths. The effect of the active fluid phase with low strontium isotopic ratios on rocks during the Patom Crater formation might lead to an abrupt decrease in values of the initial ⁸⁷Sr/⁸⁶Sr ratio in carbonized sandstones and schists.     

The geochemical evolution of the Pleistocene Lake Lisan-Dead Sea system

The geochemical history of Lake Lisan, the Pleistocene precursor of the Dead Sea, has been studied by geological, chemical and isotopic methods.Aragonite laminae from the Lisan Formation yielded (equivalent) Sr/Ca ratios in the range 0.5 × 10^?2?1 × 10^?2, Na/Ca ratios from 3.6 × 10^?3 to 9.2 × 10^?3, $\text{δ}{}^{18}\text{O}{}_{\mathrm{PDB}}$ values between 1.5 and 7%. and $\text{δ}{}^{13}\text{C}{}_{\mathrm{PDB}}$ from ?7.7 to 3.4%..The distribution coefficient of Na⁺ between aragonite and aqueous solutions, $\text{λ}{}^{\mathrm{A}}{}_{\mathrm{Na}}$, is experimentally shown to be very sensitive to salinity and nearly temperature independent. Thus, Na/Ca in aragonite serves as a paleosalinity indicator.Sr/Ca ratios and $\text{δ}{}^{18}\text{O}$ values in aragonite provide good long-term monitors of a lake's evolution. They show Lake Lisan to be well mixed, highly evaporated and saline. Except for a diluted surface layer, the salinity of the lake was half that of the present Dead Sea (15 vs 31%).Lake Lisan evolved from a small, yet deep, hypersaline Dead Sea-like, water body. This initial lake was rapidly filled-up to its highest stand by fresh waters and existed for about 40,000 yr before shrinking back to the present Dead Sea. The chemistry of Lake Lisan at its stable stand represented a material balance between a Jordan-like input, an original large mass of salts and a chemical removal of aragonite. The weighted average depth of Lake Lisan is calculated, on a geochemical basis, to have been at least 400, preferably 600 m.The oxygen isotopic composition of Lake Lisan water, which was higher by at least 3%. than that of the Dead Sea, was probably dictated by a higher rate of evaporation.Na/Ca ratios in aragonite, which correlate well with $\text{δ}{}^{13}\text{C}$ values, but change frequently in time, reflect the existence of a short lived upper water layer of varying salinity in Lake Lisan.     

Palaeohydrological significance of late Quaternary strontium isotope ratios in a tropical lake

Ostracods preserved in late Quaternary sediments of Wallywash Great Pond, a fresh coastal lake in SW Jamaica, record temporal variations in the strontium-isotope composition of lake water. Oxygen-isotope and Sr/Ca ratios in ostracods reveal temporal variations in the lake's hydrology, related to effective precipitation, and in its salinity related to varying marine-saline groundwater input from changes in relative sea level. Evaluation of isotopic and trace-element data indicates that the stratigraphic variations in ⁸⁷Sr/⁸⁶Sr ratios during the late Quaternary are best explained by climatically-controlled hydrological changes. During wetter periods, the lake's Sr budget was dominated by springwater input with relatively low ⁸⁷Sr/⁸⁶Sr ratio, whereas during drier times reduced springflow, possibly coupled with input of more-radiogenic Sr from other sources, such as sea-spray aerosols and perhaps Saharan dust, led to an increase in the Sr-isotope ratio of the lake water. Despite proximity of the lake to the sea and evidence for slight intrusion of marine saline groundwater in the past, however, the extent of marine input appears to have had limited influence on the lake's Sr-isotope ratios. Whereas the ⁸⁷Sr/⁸⁶Sr ratios cannot be used as a palaeosalinity proxy in this particular lake, they do provide valuable information about the mechanisms underlying hydrological change.     

Strontium and hydrogen isotope geochemistry of fresh and metabasalt dredged from the Mid-Atlantic Ridge

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.     

锶同位素在古岩溶研究中的应用——以塔河油田奥陶系为例

为探讨锶同位素在古岩溶研究中的应用,系统分析了塔里木盆地塔河油田奥陶系岩溶缝洞方解石的87Sr/86Sr值。研究结果表明,加里东中期岩溶形成的方解石以低87Sr/86Sr值为特征,其锶同位素组成主要由围岩的重溶锶控制。而海西早期岩溶形成的方解石则以高87Sr/86Sr值为特征,锶同位素组成主要由壳源锶和重溶锶控制;同时,不同产状的方解石锶同位素比值也不相同,渗流岩溶带的方解石比潜流岩溶带富集87Sr,主要受控于岩溶系统的渗流机制和水岩反应。在平面上,桑塔木组覆盖区比北部地区富集87Sr,其主要原因是来源于围岩的重溶锶比重加大。87Sr/86Sr值在区域上的变化,结合区域地质背景,表明海西早期岩溶对北部地区和桑塔木组覆盖区均有重要的影响,是奥陶系岩溶缝洞型储层的主要形成时期。另外,极低的锶同位素比值可能与幔源锶有关,早二叠纪末的火山活动是提供幔源锶的主要时期。通过塔河油田奥陶系古岩溶作用的实例研究,锶同位素具有良好的流体示踪能力,在划分古岩溶期次方面具有明显的优势。     

Strontium isotope composition of marine carbonates of Middle Triassic to Early Jurassic age,Lombardic Alps,Italy*

The ⁸⁷Sr/⁸⁶Sr ratios and strontium concentrations for thirty-three samples of marine carbonate rocks of Middle Triassic to Early Jurassic age have been determined. The samples were collected from four measured sections in the areas of Val Camonica in northern Italy. The strontium concentrations vary from 40 to 7000 ppm. Most of the samples are calcitic limestones containing less than 10% of non-carbonate residues. Dolomitic samples and those containing appreciable non-carbonate residues have significantly diminished strontium concentrations. ⁸⁷Sr/⁸⁶Sr ratios of the carbonate phases of these rocks appear to be unaffected by dolomitization and by the presence of non-carbonate minerals. The average ⁸⁷Sr/⁸⁶Sr ratios of the formations vary systematically in a stratigraphic sense. The ratio increased from Early Anisian to Early-Middle Ladinian, declined during Late Ladinian and Carnian, rose again during the Norian and then declined throughout the Late Norian (Rhaetian), Hettangian, Sinemurian and Pliens-bachian ages. The average ⁸⁷Sr/⁸⁶Sr ratios, relative to 0.7080 for the Eimer and Amend standard, are: Anisian: 0.70805 ± 00019; Early Ladinian: 0.7085 ± 0.00038; Late Ladinian: 0.70791 ± 0.00013; Carnian: 0.70776 ± 0.00015; Norian and Rhaetian: 0.70791 ± 0.00014; Hettangian: 0.70762 ± 0.00021; Sinemurian: 0.7070 ± 0.00038; Pliensbachian: 0.7070 ± 0.00015. These variations reflect changes in the isotopic composition of Sr entering the oceans in early Mesozoic time due to varying rates of weathering and erosion of young volcanic rocks (low ⁸⁷Sr/⁸⁶Sr) and old granitic rocks (high ⁸⁷Sr/⁸⁶Sr). The data presented in this report contribute to a growing body of information regarding the changes that have occurred in the ⁸⁷Sr/⁸⁶Sr ratio of the oceans in Phanerozoic time.     

川西坳陷新场气田须二气藏地层水成因研究——水化学和锶同位素证据

地层水是影响气田产能开发的重要因素之一,气井遇水会降低储层气相渗透率,从而导致气产量迅速下降,严重制约单井产能的提高。目前已有的研究对须二气藏地层水的物质来源认识仍然存在一定争议。本文从主微量元素、水岩相互作用以及锶同位素组成特征方面对川西坳陷新场气田须二气藏11口生产井的地层水进行了系统研究,结果显示须二气藏地层水具有低矿化度(55 166.00~122 547.41 mg/L)、高Br^-和Sr²⁺含量(分别为642.00~1 711.00 mg/L和670.00~1 780.00 mg/L)及⁸⁷Sr/⁸⁶Sr值(0.715 27~0.721 77)的特征,表明研究区地层水Sr同位素来源区别于海相碳酸盐岩,更符合砂岩风化特征。地层水中Ca的富集主要与砂岩储层成岩自生矿物的溶解有关,在深部水岩相互作用下,Sr以类质同象的方式代替Ca并且获得了有机质中的Br,同时使得Br更加富集。以上研究结果为今后该气藏赋水层位的预测提供了理论依据。     

内陆湖泊流域的化学风化及气候变化—以内蒙古岱海为例

利用湖泊沉积物中Rb/Sr值来反映受古气候制约的流域陆地化学风化率的变化，并恢复了岱海近400a以来以小冰期为特征的、具有100a准周期（经谱分析）的气候波动历史。通过磁化率、粘土矿物含量和种类的综合分析，确证了湖泊沉积物Rb/Sr值的变化可以用来重建流域内化学风化率与其相应的古气候演化过程，是湖泊沉积记录中具有比磁化率更明显气候意义的有效代用指标。