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1.
海洋Sr同位素的变化主要是由陆地河流注入的Sr同位素的变化所引起。在全球河流中,流经喜马拉雅山地河流(恒河—布拉马普特拉河)表现出与世界上其它河流明显不同的特点,具有高87Sr/86Sr、高\[Sr\]的特征。恒河—布拉马普特拉河是世界上第四大河流,是当今世界海洋Sr的重要来源。国际上,目前人们对造成喜马拉雅河流Sr异常的原因(来源)的认识,仍存较大分歧。归纳起来,主要有3种认识:一是认为来源于硅酸盐岩;二是认为来源于碳酸盐岩的风化;三是认为来源于碳酸盐岩和硅酸盐岩的风化。近年来,作者对高喜马拉雅中央结晶岩系河流Sr同位素异常及其源岩进行的研究表明,高喜马拉雅河流Sr同位素受流域地质作用的强烈影响,呈现出高87Sr/86Sr、低\[Sr\]的特点。对岩石和单矿物的研究表明,中央结晶岩系变质岩(片岩、片麻岩)和花岗岩黑云母中的87Sr/86Sr与\[Rb\]成正比并具有高87Sr/86Sr、低\[Sr\]的特征。黑云母矿物具有的易风化性,为高喜马拉雅河流放射性87Sr提供了主要来源。恒河—布拉马普特拉河的Sr异常(高87Sr/86Sr和高\[Sr\])则可能是反映了流经整个喜马拉雅造山带河流Sr混合平衡后的特征。  相似文献   

2.
贵州省地处世界岩溶发育最复杂、类型最齐全、分布面积最大的东亚岩溶区域中心, 也是我国碳酸盐岩分布面积最大、岩溶最发育的省区, 同时也是我国水土流失严重的地区之一。由于河水的地球化学反映了流域盆地的化学风化、气候和上地壳的化学组成的重要信息, 本工作对贵州喀斯特地区两条主要水系(乌江水系、沅江水系)河流的主要阴、阳离子和Sr2+离子及锶同位素组成变化进行了系统研究, 对河水地球化学组成变化特征及其控制因素进行了解释。 贵州喀斯特地区两条主要水系河流的水化学组成代表了典型碳酸盐岩地区河流的相应化学组成, 显示了与世界主要河流不同的水化学特征, 反映了喀斯特环境地表化学风化作用的特点。  相似文献   

3.
南水北调中线水源地河水地球化学特征与流域侵蚀   总被引:1,自引:0,他引:1  
丹江口水库及其上游流域是南水北调中线工程的水源地,本文讨论了水源地河流水化学与锶同位素(87Sr/86Sr)组成变化特征,目的在于了解水源地流域河流地表水溶质的物质来源以及岩石风化侵蚀过程和人为活动的影响。流域内河流水化学组成以Ca2+、HCO3-为主,Mg2+和SO42-次之,反映了碳酸盐岩风化溶解起控制作用的典型特征。水化学分析表明水源地河水受到工农业活动等人为因素的影响;河流87Sr/86Sr同位素地球化学研究表明,流域岩石风化输入至少存在三个不同端员(硅酸岩、石灰岩和白云岩)之间的混合。水源地流域内硅酸岩和碳酸岩的风化侵蚀速率分别为38.6和4.4 t/km2.a,总岩石风化侵蚀速率高于全球河流平均值。  相似文献   

4.
西江干流河水主要离子及锶同位素地球化学组成特征   总被引:8,自引:1,他引:7  
水环境中锶(Sr)含量及其同位素组成特征的研究有助于认识区域水文地球化学特征及流域盆地岩石风化速率等地球化学行为,因此河流环境中Sr的地球化学行为是地球化学研究的重要课题之一。对中国南方西江干流及其支流河水主要阴阳离子及sr同位素组成进行了分析,发现其水化学组成主要以Ca^2+、Mg^2+、HCO3^-和SO4^2-离子为主,分别占阴阳离子组成的80%以上。郁江河水具有较高的Sr同位素比值(^87St/^86Sr=0.71049)和较低的Sr含量(0.0263mg/L),而西江河水具有较低的Sr同位素比值以及较高的Sr含量,其Sr含量变化范围在0.0667.0.187mg/L之间,平均含量为0.136mg/L;Sr同位素比值变化范围在0.70856.0.70936之间,平均比值为0.70894。与世界主要河流水体中Sr含量平均值(0.078mg/L)及Sr同位素比值(^87Sr/^86Sr=0.7119)相比,西江干流水体具有较高的Sr含量及较低的Sr同位素比值。两条河流河水中主要离子及Sr的来源存在显著差异,西江干流河水中的主要溶解离子及Sr同位素主要源于碳酸盐岩(石灰岩和白云岩)的风化作用,主要受黔江及其上游红水河等化学组成所控制,而郁江则主要受碎屑岩风化作用的影响;同时,中上游地区的酸沉降及人类活动的输入可能导致西江干流水体受到一定程度的污染,而郁江受污染程度则相对较小。  相似文献   

5.
松辽盆地北部地层水同位素特征及其地质意义   总被引:1,自引:1,他引:0  
盆地流体是沉积盆地中非常活跃的因子,盆地流体的水文地球化学特征主要是受控于流体-岩石相互作用。本文以松辽盆地北部为研究对象,基于地层水的水文地球化学特征、锶-氢-氧同位素数据分析,初步探讨了水-岩反应与锶-氢-氧同位素的关系。这一研究对于丰富同位素示踪、水-岩相互作用等基础理论具有重要研究意义。分析表明,位于盆地西部地区地层水明显受到古大气降水的影响,中央凹陷地区δ18O正偏移可能是由水岩作用加强引起的。地层水为大气水与原生沉积水的混合,较轻的δD值反映出原始沉积水属陆相沉积水。地层水的87Sr/86Sr值略低而Sr2+含量又较高,是高87Sr/86Sr值流体端元与低87Sr/86Sr值流体端元的混合,即地表来源水与深部水的混合,也更多地受到高Sr2+含量低87Sr/86Sr值的火山-地热水等幔源深部水的补给。  相似文献   

6.
石灰岩化学风化显著控制着其所在流域盆地的河水Sr同位素组成,进而制约全球Sr循环。然而,石灰岩化学风化过程中Sr同位素组成的变化特征及其控制机制的研究报道依旧很少。本文通过报道粤北地区一个典型石灰岩风化剖面的Sr同位素组成变化特征,试图探讨石灰岩化学风化过程中Sr同位素变化的控制机制。结果显示:该剖面上,~(87)Sr/~(86)Sr比值介于0.70979~0.72216之间;自剖面底部到顶部,~(87)Sr/~(86)Sr比值呈现出逐渐增大的趋势;Nd同位素组成比较均一(εNd(t)=–15.0±0.5)。研究区的潜在源区(如大气降水、地表水),其~(87)Sr/~(86)Sr比值明显低于该剖面上部的最大值,加之,该剖面的风化产物与典型的中国黄土剖面具有截然不同的Sr-Nd同位素组成,暗示了这些潜在源区的输入不大可能造成该剖面上Sr同位素组成发生显著的变化。该剖面上~(87)Sr/~(86)Sr比值与Sr含量之间呈现显著的负相关性(r=–0.95),暗示粤北石灰岩化学风化过程中Sr同位素的演化受控于碳酸盐矿物与硅酸盐矿物在抗风化强度以及Sr同位素组成方面的显著差异:相对硅酸盐矿物,碳酸盐矿物(如方解石)抗风化强度较弱,于是随着风化作用的进行,原岩中具有较低~(87)Sr/~(86)Sr比值的方解石中的Sr大量迁出剖面,而具有较高~(87)Sr/~(86)Sr比值的硅酸盐矿物中的Sr残留在风化产物中,因此,随着风化强度的增加,风化产物中的~(87)Sr/~(86)Sr比值呈现出逐渐增大的趋势。  相似文献   

7.
作者于2000年和2002年对青藏高原东部长江河流溶质载荷进行了较为系统的野外取样工作,并对主要离子地球化学特征进行了分析研究。数据分析表明,长江水系TZ 高于世界河流1250μEq的平均值,主要介于2000~3000μEq之间,其次为1000~2000μEq。总体上,高原东部长江水系TZ 可以与世界上其它造山带相比较。高原东部长江水系主要阴离子的相对丰度和分布表现出HCO3->Si Cl- SO42-,河水富含HCO3-;阳离子主要表现为Ca2 >Mg2 Na K ,表明河水富含Ca离子特征。河水中富含HCO3-和Ca2 ,说明高原东部长江水系流域盆地中碳酸盐岩(主要是灰岩)应是河流中主要离子的风化源岩。  相似文献   

8.
喀斯特河流溶解态稀土元素组成变化及其控制因素   总被引:8,自引:0,他引:8  
韩贵琳  刘丛强 《中国岩溶》2004,23(3):177-186
以化学萃取-反萃取分离法为手段,结合等离子质谱分析仪测量了喀斯特地区乌江、沅江两大水系的枯水期河流的溶解态稀土元素含量.该两河流的化学组成代表了流经碳酸盐岩地层的河水的化学组成.与世界其它地区低pH的河水不同,喀斯特地区河水溶解态稀土元素含量较低,页岩标准化配分模式并不平坦,轻、重稀土元素分异因河流的不同而不同,乌江水系上游轻稀土元素(LREE)相对重稀土元素(HREE)富集,中下游HREE相对于LREE富集,沅江水系河水HREE相对于LREE富集,页岩标准化配分模式具明显的Ce、Eu负异常.乌江、沅江及其支流有高的溶解盐,含有较高的溶质浓度,河水水化学(高碱度、高离子含量、高pH值)和水/粒相互作用控制了喀斯特河水中溶解态稀土元素的含量和轻、重稀土元素的分异.  相似文献   

9.
青藏高原东部金沙江流域盆地陆地风化特征   总被引:2,自引:0,他引:2       下载免费PDF全文
青藏高原东部金沙江流域是研究高原隆升与陆地风化的理想地区。本文通过对金沙江河流系统的取样,从河流溶质载荷主要离子和悬浮载荷粘土矿物等方面揭示青藏高原东部金沙江流域盆地陆地风化特征。研究表明,金沙江流域盆地陆地岩石风化主要是碳酸盐岩、蒸发盐岩和硅酸盐岩。利用S i、S i/TZ+*、S i/Na*+K和S i/K以及(Na*+K)/TZ+等5个指标结合流域区域岩石分布和土壤特征揭示出流域硅酸盐岩为浅表性初级风化,风化产物主要是富含阳离子的次生粘土矿物。  相似文献   

10.
岩石风化碳汇是全球碳汇的重要组成部分,通过对赤水河流域水体主要离子组成进行测定,分析赤水河流域河水水化学特征及其岩石风化过程对大气CO_2的消耗。结果表明:赤水河流域离子组成以Ca~(2+),Mg~(2+),HCO_3~-和SO_4~(2-)为主,河水总溶解性固体(TDS)含量均值为317.88 mg/L,高于全球流域均值(65 mg/L)。元素比值分析表明赤水河流域离子组成主要受岩石风化控制,其中碳酸盐岩风化为主导控制因素,碳酸盐岩、硅酸盐岩对河水溶质贡献率分别为70.77%和5.03%。人类活动和大气降水对流域河水溶质的贡献很小。流域岩石化学风化速率为126.716 t/(km~2·a),高于黄河、长江、乌江及世界河流均值。流域岩石化学风化对大气CO_2的消耗量为10.96×10~9mol/a,岩石风化对大气CO_2消耗速率为5.79×10~5mol/(km~2·a),与长江流域接近,高于黄河流域。  相似文献   

11.
岩溶水锶元素水文地球化学特征   总被引:12,自引:9,他引:12  
通过对桂林地区地下河系统不同类型岩溶水水样Sr2 含量和87Sr/86Sr值分析,得到如下结论:(1)桂林地区岩溶水中Sr2 含量普遍较低,流经不同岩层的地下水Sr2 含量不同,岩溶水中Sr2 含量随着Ca2 含量的增大而增大,随着Mg2 含量的增大而减小;地下河水中的Sr2 含量始终介于表层岩溶带水、饱水带裂隙水、地表坡面流和外源水(如果存在外源水补给)的最大、最小值之间.(2)流经不同岩层地下水的87Sr/86Sr值不同,流经砂岩层地下水87Sr/86Sr值较高,其次为流经白云岩层和灰岩层的地下水;地下河水87Sr/86Sr值也是介于表层岩溶带水、饱水带裂隙水、地表坡面流和外源水(如果有外源水补给)的最大、最小值之间.因此Sr2 和87Sr/86Sr能反映岩溶水形成的信息,是较理想的天然示踪剂,在岩溶水研究中具有很广阔的应用前景.  相似文献   

12.
为深入评估中国南方陆地风化过程及河流物质循环过程, 通过测定西江主要干、支流丰水期及枯水期水体主要离子和锶及其同位素比值, 结合Galy模型对西江流域化学风化特征及CO2消耗通量进行计算。结果表明: (1)西江流域化学风化受人类活动的影响较小, 流域化学风化过程主要受到碳酸的控制。(2)河水阳离子的主要物质来源为硅酸盐岩和碳酸盐岩风化, 硅酸盐岩在丰水期和枯水期的阳离子物质来源摩尔占比均为0.04, 碳酸盐岩中石灰岩占比分别为0.79和0.78, 白云岩分别为0.17和0.18。(3)西江流域在丰水期和枯水期的化学风化过程具有一定的差异性, 由于硫酸参与白云岩的风化作用影响碳酸盐岩风化过程中的CO2消耗通量, 导致各个化学风化过程所涉及的CO2通量有所差别。(4)碳酸风化碳酸盐岩在丰水期和枯水期所消耗的CO2通量分别为(0.78~244.25)×106 mol/km2/yr和(0.10~49.16)×106 mol/km2/yr, 硫酸风化碳酸盐岩所产生的CO2通量分别为(0.25~42.16)×106 mol/km2/yr和(0.01~13.90)×106 mol/km2/yr, 碳酸风化硅酸盐岩所消耗CO2通量的分别为(0.05~17.83)×106 mol/km2/yr和(0.02~6.07)×106 mol/km2/yr。  相似文献   

13.
The main scope of this study is to investigate parameters controlling chemical weathering rates for a large river system submitted to subarctic climate. More than 110 river water samples from the Mackenzie River system (northern Canada) have been sampled and analyzed for major and trace elements and Sr isotopic ratios in the dissolved phase. The three main morphological units are reflected in water chemistry. Rivers from the Canadian Shield are very dilute, dominated by silicate weathering (Millot et al., 2002), whereas the rivers of the Rocky and Mackenzie Mountains as well as the rivers of the sedimentary Interior Platform are dominated by carbonate weathering and are SO4 rich. Compared to the rivers of the Mackenzie and Rocky Mountains, the rivers of the interior plains are organic, silica, and Na rich and constitute the dominant input term to the Mackenzie River mainstream. Rivers of the Canadian Shield area do not significantly contribute to the Mackenzie River system. Using elemental ratios and Sr isotopic ratios, a mathematical inversion procedure is presented that distinguishes between solutes derived from silicate weathering and solutes derived from carbonate weathering. Carbonate weathering rates are mostly controlled by runoff, which is higher in the mountainous part of the Mackenzie basin. These rates are comparable to the carbonate weathering rates of warmer areas of the world. It is possible that part of the carbonate weathering is controlled by sulfide oxidative weathering, but its extent remains difficult to assess. Conversely to what was stated by Edmond and Huh (1997), overall silicate weathering rates in the Mackenzie basin are low, ranging from 0.13 to 4.3 tons/km2/yr (Na + K + Ca + Mg), and confirm the negative action of temperature on silicate weathering rates for river basins in cold climates. In contrast to what has been observed in other large river systems such as the Amazon and Ganges Rivers, silicate weathering rates appear 3 to 4 times more elevated in the plains than in the mountainous headwaters. This contradicts the “Raymo hypothesis” (Raymo and Ruddiman, 1992). Isotopic characterization of suspended material clearly shows that the higher weathering rates reported for the plains are not due to the weathering of fine sediments produced in the mountains (e.g., by glaciers) and deposited in the plains. Rather, the relatively high chemical denudation rates in the plains are attributed to lithology (uncompacted shales), high mechanical denudation, and the abundance of soil organic matter derived from incomplete degradation and promoting crystal lattice degradation by element complexation. The three- to fourfold factor of chemical weathering enhancement between the plains and mountains is similar to the fourfold factor of enhancement found by Moulton et al. (2000) between unvegetated and vegetated watershed. This study confirms the negative action of temperature on silicate weathering for cold climate but shows that additional factors, such as organic matter, associated with northern watersheds are able to counteract the effect of temperature. This acceleration by a factor of 4 in the plains is equivalent to a 6°C increase in temperature.  相似文献   

14.
Winter seasonal concentrations of dissolved rare earth elements (REE) of two major river systems (the Wujiang River system and the Yuanjiang River system) in karst-dominated regions in winter were measured by using a method involving solvent extraction and back-extraction and subsequent ICP-MS measurements. The dissolved REE concentrations in the rivers and their tributaries are lower than those in most of the large rivers in the world. High pH and high cation (i.e., Na+ + Ca2+) concentrations of the rivers are the most important factors controlling the concentrations of dissolved REE in the river water. The dissolved load (<0.22 μm) REE distribution patterns of high-pH river waters are very different from those of low-pH river waters. The shale (PAAS)-normalized REE patterns for the dissolved loads are characterized by light REE-enrichment and heavy REE-enrichment. Water in the upper reaches of the Wujiang River generally shows light REE-enriched patterns, while that in the middle and lower reaches generally shows heavy REE-enriched patterns. The Yuanjiang River is heavy REE enriched with respect to the light REE in the same samples. Water of the Wuyanghe River draining dolomite-dominated terrains has the highest heavy REE-enrichment. Most river water samples show the shale-normalized REE patterns with negative Ce and Eu anomalies, especially water from Wuyanghe River. Y/Ho ratios show that the water/particle interaction might have played an important role in fractionation between HREE and LREE.  相似文献   

15.
为了掌握亚热带季风气候岩溶地区流域水化学变化特征及量化流域内岩石化学风化过程对吸收大气CO2的贡献,文章选取湘西峒河流域作为研究对象,于2016年7—8月对研究区干流和7个子流域进行了水样采集与分析。结果表明:河水pH平均值为8.31,总体呈偏碱性。EC与TDS的变化范围较大,这主要与流域内岩性的分布有关。水中离子以Ca2+、HCO-3为主,水化学类型为HCO3—Ca型,岩性控制水化学的组成。HCO-3、Ca2+和Mg2+主要来源于碳酸盐岩的风化,其余离子来源多受人为活动影响。峒河流域干流的主要离子中,HCO-3、Ca2+和Mg2+浓度从上游至下游总体下降,反映了河流从碳酸盐岩区流向碎屑岩为主地层的过程。NO-3、K+、Na+、F-、Cl-和SO2-4呈增长趋势,说明峒河受人为污染影响较大,反映出人为活动的密集程度。通过子流域的划分可知流域上游主要受灰岩以及白云岩控制,中游以灰岩控制为主,下游受砂岩、泥岩及碎屑岩控制为主。收集流域最终出口吉首观测站一个水文年的数据并运用水化学—径流法估算出峒河流域无机碳通量为60 477.33 tCO2/a,碳汇强度为71.15 tCO2/(km2·a)。  相似文献   

16.
The influx of Sr responsible for increase in marine Sr has been attributed to rise of Himalaya and weathering of the Himalayan rocks. The rivers draining Himalaya to the ocean by the northern part of the Indian sub-continent comprising the Ganga Alluvial Plain (GAP) along with Central parts of the Himalaya and the northern part of the Indian Craton are held responsible for the transformation of Sr isotopic signature. The GAP is basically formed by the Himalayan-derived sediments and serves as transient zone between the source (Himalaya) and the sink (Bay of Bengal). The Gomati River, an important alluvial tributary of the Ganga River, draining nearly 30,500 km2 area of GAP is the only river which is originating from the GAP. The river recycles the Himalayan-derived sediments and transport its weathering products into the Ganga River and finally to Bay of Bengal. 11 water samples were collected from the Gomati River and its intrabasinal lakes for measurement of Sr isotopic composition. Sr concentration of Gomati River water is about 335 μg/l, which is about five times higher than the world’s average of river water (70 μg/l) and nearly three times higher than the Ganga River water in the Himalaya (130 μg/l) The Sr isotopic ratios reported are also higher than global average runoff (0.7119) and to modern seawater (0.7092) values. Strong geochemical sediment–water interaction appearing on surface is responsible for the dissolved Sr isotopic ratios in the River water. Higher Sr isotopic rations found during post-monsoon than in pre-monsoon season indicate the importance of fluxes due to monsoonal erosion of the GAP into the Gomati River. Monsoon precipitation and its interaction with alluvium appear to be major vehicle for the addition of dissolved Sr load into the alluvial plain rivers. This study establishes that elevated 87Sr/86Sr ratios of the Gomati River are due to input of chemical weathering of alluvial material present in the Ganga Alluvial Plain.  相似文献   

17.
贵阳市区地表/地下水化学与锶同位素研究   总被引:7,自引:0,他引:7       下载免费PDF全文
贵阳市及邻近地区地表和地下水的化学与Sr同位素组成变化反映了典型喀斯特地区地表/地下水文系统的水-岩反应和城市污染特征:水体中的化学溶解物质主要来源于碳酸盐岩(石灰岩和白云岩)的风化作用和膏岩层的溶解,其次为人为污染物的输入;污染物以K+,Na+,Cl-,SO2-4,NO-3为主,枯水期因大气降水补给小而受人为活动影响较大;丰水期和枯水期地表/地下水的化学组成变化说明地表/地下水交换活跃,地下水环境容易受到人为活动影响。  相似文献   

18.
Groundwater quality in karst regions is largely controlled by natural processes and anthropogenic activities. Over the past 10?years, dissolved Sr and its radiogenic isotope, 87Sr/86Sr, were widely used to trace the sources of solutes in groundwater. However, there is little research about hydrogeochemistry and Sr isotopic compositions of the karst groundwater in Chongqing karst area. In this paper, thirty-five representative karst groundwater samples were collected from different aquifers (limestone and dolomite) and various land use types. Hydrochemical types of karst groundwater in Chongqing were mainly of the Ca-HCO3 type or Ca(Mg)-HCO3 type. The dissolved Sr concentrations of the studied groundwater ranged from 0.57 to 15.06???mmol/L, and the 87Sr/86Sr varied from 0.70751 to 0.71627. The groundwater samples from different aquifers and land use types showed distinctive dissolved Sr concentrations and 87Sr/86Sr. The very positive relationship between Ca/Sr and Mg/Sr in dolomite and limestone aquifers suggests that Ca, Mg and Sr element come mainly from the release of carbonate rock under the groundwater?Crock?CCO2 gas interaction. According to the 87Sr/86Sr ratio, the Sr element in karst groundwater in Chongqing was controlled by the weathering of limestone, dolomite and silicate rock (allogenic water in a non-karst area). The relationship 87Sr/86Sr versus Sr2+/[K+?+?Na+] shows that the anthropogenic inputs also obviously contribute to the Sr contents. The research results show that the karst groundwater in Chongqing is facing serious crisis of water quality, and needs to be protected further.  相似文献   

19.
Filtered subglacial meltwater samples were collected daily during the onset of melt (May) and peak melt (July) over the 2011 melt season at the Athabasca Glacier (Alberta, Canada) and analyzed for strontium-87/strontium-86 (87Sr/86Sr) isotopic composition to infer the evolution of subglacial weathering processes. Both the underlying bedrock composition and subglacial water–rock interaction time are the primary influences on meltwater 87Sr/86Sr. The Athabasca Glacier is situated atop Middle Cambrian carbonate bedrock that also contains silicate minerals. The length of time that subglacial meltwater interacts with the underlying bedrock and substrate is a predominant determining factor in solute concentration. Over the course of the melt season, increasing trends in Ca/K and Ca/Mg correspond to overall decreasing trends in 87Sr/86Sr, which indicate a shift in weathering processes from the presence of silicate weathering to primarily carbonate weathering.Early in the melt season, rates of carbonate dissolution slow as meltwater approaches saturation with respect to calcite and dolomite, corresponding to an increase in silicate weathering that includes Sr-rich silicate minerals, and an increase in meltwater 87Sr/86Sr. However, carbonate minerals are preferentially weathered in unsaturated waters. During the warmest part of a melt season the discharged meltwater is under saturated, causing an increase in carbonate weathering and a decrease in the radiogenic Sr signal. Likewise, larger fraction contributions of meltwater from glacial ice corresponds to lower 87Sr/86Sr values, as the meltwater has lower water–rock interaction times in the subglacial system. These results indicate that although weathering of Sr-containing silicate minerals occurs in carbonate dominated glaciated terrains, the continual contribution of new meltwater permits the carbonate weathering signal to dominate.  相似文献   

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