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1.
南海表层沉积物的稀土和微量元素的丰度及其空间变化   总被引:6,自引:0,他引:6  
对南海表层沉积物中稀土元素、微量元素丰度和分布特征的研究结果表明,在空间分布上,∑REE与Nb、,Th、Ta、Rb、Ti、Zr、Hf、Cs、Ga、Li等相似,呈显著正相关,反映出这些元素在风化、搬运和沉积过程中地球化学行为非常相似;元素Sr几乎与所有元素都呈负相关,指示其来源或存在形式不同于其他元素,主要来源于生物作用,而在粗粒级的钙质生物贝壳和碎屑中富集.∑REE与Nb、Th、Ta、Rb、Ti、Zr、Hf、Cs、Ga、Li在陆架区具有沿陆分带特点,北部陆架区、中南半岛中东部和加里曼丹岛西北部沿大陆区域富集,与该区陆源河流物质输入及海流的分选作用,造成某些富含稀土和微量元素的重砂矿的富集有关;西南部巽他陆架和东南部岛礁区以及中、西沙附近区域含量较低,与该区域的生源碳酸盐的稀释作用,使粘土矿物相对减少和火山物质对其产生的“稀释“作用有关.南海各海区沉积物和全海区表层沉积物平均值的球粒陨石标准化稀土元素分布模式,总体上与中国大陆沉积物和浅海沉积物相似,而与大洋玄武岩完全不同,反映了南海沉积物与中国浅海沉积物及中国大陆沉积物的物源大致相同,主要来自陆源.南海各海区沉积物稀土元素的球粒陨石标准化配分曲线仍表现出了一定差异,陆架区轻稀土比重稀土明显富集,存在比较明显的Eu负异常,与陆架区相比较,陆坡区和海盆区则轻稀土含量相对降低,重稀土含量有所上升,LREE/HREE从陆架区、陆坡区到海盆区逐渐降低,显示陆架区主要为陆源,而陆坡和海盆沉积物中则有幔源物质加入.稀土元素的大陆壳标准化配分模式大部分较为平坦,少数样品呈轻稀土弱富集型或重稀土弱富集型.说明南海海表层沉积物主要来源于周边大陆.从各海区沉积物稀土元素的大陆壳标准化配分曲线对比来看,陆架区表现为轻稀土富集、重稀土亏损,具一定的铕负异常,深部海盆区则出现明显的中稀土和重稀土的富集,铕异常变弱,与深部海盆区有基性火山物质的加入的地质事实相吻合.南海表层沉积物稀土元素和微量元素总体上呈现出以陆源沉积为主的特征.其元素平均丰度和各参数值都比较接近陆源河流和中国浅海沉积物,而与深海沉积物和大洋玄武岩差别显著,显示南海沉积物虽然受到火山沉积和生物沉积的混合作用的影响,但其物质源仍然主要来自于周缘大陆.  相似文献   

2.
利用电感耦合等离子体质谱 (ICP- MS)和电感耦合等离子体原子发射光谱 (ICP- AES)方法分析了常规碱液提取海洋沉积物中的生物硅所获取的溶液中的 Si、 Al和 Ti含量.分析结果显示 , 碱液提取法获取的溶液中 Si和 Al明显地由两种来源混合而成,其中, Si有较大比例的陆源碎屑成分的贡献,并不能直接代表沉积物中的生物硅含量,而需要对其中的陆源碎屑贡献进行扣除.通常使用 Al来代表陆源碎屑进行扣除的方法无法给出正确结果,因为碱提取液中 Al存在明显的非碎屑组分.对数个土壤及水系沉积物标准样品物质的试验发现,碱提取可以优先溶解其中的 Si和 Al,而提取液中的 SiO2/TiO2比值相对于土壤和沉积物全样的 SiO2/TiO2比值有一个比较固定的富集系数 (约 14左右 ).对南海沉积物而言,根据这个富集系数和区域的碎屑物质的化学组成算得碱提取液中碎屑组分 SiO2/TiO2比值约为 748,这与根据二端员混合估计的比值相当.这样,根据提取液中的 Ti含量可以较好地扣除出碎屑组分对生物硅的污染,对于更准确测定海洋沉积物中低含量的生物硅具有重要意义.  相似文献   

3.
曲华祥  黄宝琦 《地学前缘》2019,26(3):236-242
海洋沉积物中的某些主微量元素与沉积物源区有着密切的联系,它们之间的比值变化受到源区化学风化强度的影响,因此这些元素的比值变化可以反映出海洋沉积物源区古气候的变化。本文研究了南海北部陆坡MD12-3432站位深海氧同位素6期和5期(MIS6/5) 沉积物的主微量元素,发现其表现出良好的气候控制变化特征,K/Ti、Mg/Ti、Al/Ti、Fe/Ti、Co/Ti、Zn/Ti和V/Ti等比值在MIS 5期时较高,而在MIS6期时较低。南海北部的碎屑物质主要来自中国华南地区,沉积物中元素比值的变化表明间冰期时(MIS5)华南地区陆壳化学风化增强,说明该时期华南陆地气候环境温暖湿润,这可能是间冰期时东亚夏季风加强的结果;而冰期时南海北部沉积物源区化学风化减弱,则与此时东亚冬季风较强,华南地区气候干燥寒冷相关。同时,与表层海水生产力相关的Ba/Ti比值在间冰期较高而冰期较低,反映出南海北部在间冰期时表层生产力较高而冰期时相对较低,这可能是由于东亚夏季风增强带来更多降雨,陆地化学风化作用加强,大量营养成分随河流进入南海,导致南海北部表层海水生产力增加。  相似文献   

4.
通过对南海西部上升流区MD05-2899孔开展高分辨率碳酸盐地层学和XRF岩芯扫描元素地球化学分析,重建了晚第四纪54万来以来东亚夏季风的演化历史,探讨海平面升降对南海西部陆源碎屑供应量的影响。研究选用了ln(Ba/Al)作为该海区古生产力的指标,ln(Br/Al)作为有机物的指标,ln(Ti/Al)作为陆源碎屑供应量的指标。研究结果显示,东亚夏季风在过去54万年以来强度不断增强,具有明显的冰期—间冰期旋回特征,在间冰期强盛和冰期减弱,是控制该海区有机物含量变化的主要因素。东亚夏季风不断强盛可能直接导致了南海周边陆地降雨增强,河流径流量加大,使得南海西部上升流区域的陆源碎屑供应量在间冰期明显高于冰期。研究发现,当相对海平面低于-60 m的时候,大面积暴露的巽他陆架可能向南海西部深水区输入大量陆源碎屑物质,造成研究站位的陆源碎屑供应量在冰盛期出现高值。因此,晚第四纪的东亚夏季风演化和海平面升降共同控制了南海西部上升流区陆源碎屑物质供应量的变化。  相似文献   

5.
南海沉积物中过剩铝问题的探讨   总被引:13,自引:0,他引:13  
本分析了南海两个沉积物柱样的全、酸溶解残余物质和酸溶解组分的Al2O3、TiO2含量和Al/Ti值,结果显示其存在明显的非碎屑A1组分(占沉积物总A1含量的20%—70%)。因此通常使用沉积物的Al含量来估算陆源碎屑的比例可能会导致过高的结果。而TI则不存在自生富集现象,是估算陆源碎屑比例的最佳代用指标。  相似文献   

6.
刘家峡水库表层沉积物微量元素地球化学特征   总被引:1,自引:1,他引:0       下载免费PDF全文
采用多元统计的方法对刘家峡水库表层沉积物中25种微量元素的含量、相关性、来源及控制因素进行了分析。结果显示:研究区表层沉积物中Sr、Zn、Zr和Ba的含量平均值超过了170μg/g,Cd、Mo和Tl的含量平均值都在1μg/g以下,其它元素含量平均值则在2. 01~104. 34μg/g。元素Cu、V、Co、Cr、Ni、Rb、Li、Cd、Be、Pb、Sc、As、Ga、Nb、Sn、Cs、Tl、Th和Al2O3等存在较为明显的相关性,且它们分布规律基本相似。因子分析表明,水库中微量元素分为3个主要来源,第一组分的元素分布受控于矿物岩石的自然风化剥蚀,其贡献率为63. 20%;第二组分的Zr和Ba主要受河流沉积物中元素的迁移和转化的影响,其贡献率为12. 51%;第三组分的Sr则主要受控于生物成因,其贡献率为9. 76%。另外,研究区重金属元素中,Zn和As含量远超过了全球页岩平均值,值得进一步的深入研究。  相似文献   

7.
任景玲  张经  刘素美 《地球科学进展》2005,20(12):1314-1320
地球化学家通常用Al对其它重金属进行归一化以校正沉积物来源、粒度、矿物组成等方面的影响,因此现代海洋沉积物样品中Al、Ti含量的结果主要用于定量描述陆源输送的贡献。近期研究结果发现,在受陆源物质输送影响较小,沉降颗粒主要以生源颗粒物为主的赤道大洋区,沉积物中出现明显的“过剩铝”信号,“过剩铝”约占沉积物中总铝含量的50%。因此,用沉积物中Al的含量来估算陆源碎屑的比例会导致过高的结果,建议用Ti、Sc作为参比元素校正陆源物质的影响。沉积物中的Al/Ti比值可用来示踪水体中颗粒物的沉降通量和初级生产的改变。综述了近期以Al/Ti比值这种新的地球化学示踪剂反演古生产力的最新研究进展,提出了在我国陆架边缘海开展此项工作可能存在的问题与挑战。  相似文献   

8.
南海北部陆架海域表层沉积物地球化学特征及地质意义   总被引:2,自引:0,他引:2  
赵利  蔡观强  钟和贤  等 《江苏地质》2017,41(1):103-111
依据南海北部陆架海域225个站位表层沉积物粒度和常量元素的地球化学分析,探讨了常量元素的空间分布规律及地质意义。该区域沉积物主要为粉砂、细砂等细粒沉积,平均粒径5.38。沉积物常量元素组合以SiO2、Al2O3、Fe2O3、MgO、CaO、Na2O、K2O为主,约占沉积物总量的87.96%,其空间分布特征与沉积物类型密切相关。Al2O3、Fe2O3、MgO、K2O、Org.C等分布趋势相似,具有较好的相关性,倾向于富集在细粒沉积物中;SiO2、CaO、CaCO3与大多数元素呈负相关,倾向于富集在粗颗粒沉积物中,反映了“元素的粒度控制律”。元素总体分布规律显示沉积物的常量元素含量受细粒黏土矿物吸附作用、石英矿物和碳酸钙稀释作用的共同影响。元素统计结果表明,表层沉积物的常量元素大体可分为2类:第1类包括Al2O3、Fe2O3、MgO、TiO2、P2O5、MnO等,代表陆源较细粒碎屑沉积,是控制研究区沉积物化学成分的最主要因素;第2类主要包括CaO、CaCO3,代表海洋生物沉积。同时可将研究区分为3个沉积区域:I沉积区为粤西近岸及北部湾北部区域,具有明显陆源碎屑沉积特征;Ⅱ沉积区位于粤西陆架水深>60 m海域,受海源生物作用明显;Ⅲ沉积区位于珠江口西南部水深40~60 m海域,为斑块状砾质粗粒沉积。  相似文献   

9.
邹亮  韦刚健 《地球化学》2009,38(1):89-95
通过对南海北部ODP1148站岩芯454.8mcd以上(约23.2Ma以来)的175个沉积物样品中CaCO3以及生物成因Ba含量变化的研究,并结合初期对ODP1148站岩芯分析的一些相关地球化学组成结果,探讨了碳酸盐、生物成因Ba作为海洋古生产力指标的影响因素,以及早中新世以来南海北部陆坡古生产力的变化特征。结果显示,除中新世早期(23~21.4Ma)以外,生物成因Ba与CaCO3含量和沉积速率变化有很好的相关性,反映南海北部古生产力变化波动较大。对钻孔中生物成因Ba的研究表明,在沉积埋葬以及埋葬后的保存过程中(特别是在320mcd以下)。生物成因Ba会在少氧或缺氧环境下发生还原反应而迁移,影响了它在古环境研究当中的作用。另外,结合钻孔中CaCO3含量变化的数据,在南海北部陆坡,CaCO3的溶解作用并不是很强,其沉积后保存良好,可作为研究南海北部古生产力的基础性指标。  相似文献   

10.
青海湖沉积物生物硅的环境意义初步研究   总被引:1,自引:0,他引:1  
湖泊沉积物中生物硅含量的变化已经被广泛应用于评价湖泊生产力和古气候变化研究,但大型湖泊不同位置生物硅含量的时空变化及其与环境要素之间的关系仍缺乏详细的现代过程研究.通过对青海湖不同位置表层沉积样品的生物硅含量测定,建立其空间分布模式及最近数百年生物硅含量的时间序列.结果表明,青海湖表层沉积物生物硅含量变化范围是1.75%~2.98%,平均值为2.25%.与世界其他湖泊相比,青海湖生物硅含量处于相对较低水平,可能与其特殊的地理位置和气候条件有关.青海湖生物硅含量的空间分布规律与沉积物质量堆积速率以及陆源组分含量(如SiO2)相反,而与化学/生物沉积组分(如CaCO3)含量的空间分布规律大体一致,说明生物硅的空间分布受到陆源碎屑物质的"稀释效应"影响.时间序列上,生物硅含量与SiO2含量呈相反变化趋势,与指示降雨量变化的C/N比值也是反相变化,说明生物硅含量在时间序列上也受与气候条件密切相关的陆源输入的影响.青海湖湖心低沉积速率区域的生物硅指标具有指示古气候变化的潜力.  相似文献   

11.
We analyzed 77 surface sediment samples collected in the southwestern East/Japan Sea from the Korea Strait through the Ulleung Basin and the Korea Plateau for grain size, calcium carbonate, organic carbon, and major (Na, Mg, Al, Fe, K, Ca, and Ti) and trace elements (P, Mn, Sr, Li, Sc, V, Cr, Co, Ni, Zn, Cu, and Pb).The chemical composition of the surface sediments was found to be highly variable spatially. Cluster analysis of surface sediment chemical compositions indicated five major geochemical sedimentary environments: basin, lower slope, coast and upper slope, inner shelf, and outer shelf. Continental-shelf sediments were rich in shell fragments and had relict and coarse-grained characteristics. Recent fine-grained sediments were only distributed in coastal, slope, and basin areas. Concentrations of Al, K, Ca, Ti, Cr, and Sc were highest in the coastal and upper slope areas and decreased with water depth. Elemental ratios using major and trace elements indicated that coastal and upper slope detrital sediments were mixtures of sediments derived from the Changjiang (Yangtze) and Nakdong Rivers. Although the concentrations of organic carbon, P, Mn, V, Co, Ni, Cu, and Pb increased with water depth, their distribution patterns indicated authigenic (V, Cu, and Pb) and diagenetic (Fe, P, Mn, Co, and Ni) origins. The distribution pattern with water depth suggested that the chemical composition of surface sediment was determined by sedimentologic and geochemical processes, such as the supply of detrital and biogenic materials, and authigenic and post-depositional diagenetic processes in sediments.  相似文献   

12.
利用电感耦合等离子体质谱仪测定了中国南极科考21~27航次期间获取的普里兹湾表层沉积物中Cu、Pb、Zn、Cd、Cr、Co、Al、Fe、Mn的含量,分析了普里兹湾微量元素的分布特征,结合沉积物粒度分布、生物硅含量,并利用富集系数和主成分分析的方法,探讨了微量元素的物源指示意义。研究结果表明:普里兹湾沉积物中的微量元素含量与南大洋其他海域具有很好的可比性。Cu、Zn、Cr、Co、Fe、Mn含量在陆坡深海区明显高于冰架边缘区和陆架区;Al、Pb含量在冰架边缘区较高;而Cd含量在陆架区相对较高。人类活动对普里兹湾沉积物中的微量元素没有明显的影响,南极大陆岩石风化产物和海洋生物源性沉降是其主要来源。冰架边缘区及陆架破折处P2-9站位的微量元素主要为岩源性输入。陆架区、陆坡深海区的微量元素Cu、Zn、Cr、Co、Fe、Mn明显受到生源性物质输入的影响。而普里兹湾沉积物中Cd则主要来源于硅藻的吸收利用及硅质软泥的富集。  相似文献   

13.
蒋富清  李安春 《沉积学报》2002,20(4):680-686
对冲绳海槽南部陆架、陆坡和海槽 33个表层沉积物进行了元素地球化学分析,结果表明研究区沉积物的主要化学组成为SiO2 、Al2 O3 和CaO,这三种组分占沉积物总量的 6 8%左右。多数元素在陆架和陆坡的变化范围较大,在海槽区相对稳定。向海槽方向随沉积物粒径变细,SiO2 和CaO减少、Al2 O3 和其它多数元素含量增加。常量元素和Al2 O3 的比值分布特征表明,本区沉积物由物源区经由陆架向海槽输送,沉积物主要由陆源碎屑沉积组成,此外还有生物碎屑沉积和自生沉积。陆架区部分微量元素富集因子 (EF)与长江和黄河沉积物的富集因子对比结果表明,本区的沉积物与长江沉积物的关系更为密切。陆坡区Cu、Pb、Zn、Co、Ni和Cr的富集因子较高是由于生物的富集作用造成的,Mn的富集主要是自生沉积的结果。用R型因子分析方法对沉积物的化学组成进行了分析,结合元素的分布特征,给出了四个主因子所对应的沉积环境和特征元素组合,分别为 1)陆架型的元素组合 :SiO2 、TiO2 、Zr、CaO和Sr,2 )陆坡型的元素组合Fe2 O3 、MgO和P2 O5,3)海槽型的元素组合 :Al2 O3 、K2 O、Cu、Zn、Co、Ni、Cr和Ba,4 )反映沉积环境氧化-还原属性的元素组合 :MnO和FeO。  相似文献   

14.
右江盆地位于华南板块西南缘与印支板块的结合部位,于中三叠世沉积了一套以细碎屑岩为主的巨厚浊积岩。研究区中三叠统细碎屑岩的主量、微量和稀土元素分析表明,细碎屑岩以杂砂岩和岩屑砂岩为主,其源岩来自大陆上地壳,物源区岩石类型主要为长英质沉积岩和火成岩,岩石风化程度中等偏高,构造背景为大陆岛弧和活动大陆边缘。综合细碎屑岩稀土元素特征及前人对该区中三叠统古流向和碎屑锆石U-Pb年代学研究,认为中三叠统碎屑物来源复杂,云开地区、江南造山带和越北地块是主要的物源区。  相似文献   

15.
Surface slices of 20 sediment cores, off southwestern Taiwan, and bed sediment of River Kaoping were measured for major and trace elements (Al, As, Ca, Cd, Cl, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, S, Si, Ti, V, and Zn) to evaluate the geochemical processes responsible for their distribution, including elemental contamination. Major element/Al ratio and mean grain size indicate quartz-dominated, coarse grained sediments that likely derived from sedimentary rocks of Taiwan and upper crust of Yangtze Craton. Bi-plot of SiO2 versus Fe2O3T suggests the possible iron enrichment in sediments of slag dumping sites. Highest concentrations of Cr, Mn, P, S, and Zn found in sediments of dumping sites support this. Correlation analysis shows dual associations, detrital and organic carbon, for Cr, P, S, and V with the latter association typical for sediments in dumping sites. Normalization of trace elements to Al indicates high enrichment factors (>2) for As, Cd, Pb, and Zn, revealing contamination. Factor analysis extracted four geochemical associations with the principal factor accounted for 25.1% of the total variance and identifies the combined effects of dumped iron and steel slag-induced C–S–Fe relationship owing to authigenic precipitation of Fe–Mn oxyhydroxides and/or metal sulfides, and organic matter complexation of Fe, Mn, Ca, Cr, P, and V. Factors 2, 3, and 4 reveal detrital association (Ti, Al, Ni, Pb, Cu, and V), effect of sea salt (Cl, Mg, Na, and K) and anthropogenic component (As and Zn)-carbonate link, respectively, in the investigated sediments.  相似文献   

16.
Suboxic trace metal geochemistry in the Eastern Tropical North Pacific   总被引:3,自引:0,他引:3  
We analyzed Al, Ti, Fe, Mn, Cu, Ba, Cd, U, Mo, V, and Re in water column, settling particulate, and sediment (0 to 22 cm) samples from the intense oxygen minimum zone (OMZ) of the eastern tropical North Pacific near Mazatlán, Mexico. The goal was to determine how the geochemistry of these elements was influenced by suboxic water column conditions and whether the sediments have a unique “suboxic” geochemical signature.The water column was characterized by a Mn maximum, reaching ∼8 nmol kg−1 at 400 m. Concentrations of Cu, Ba, Cd, Mo, Re, U, and V were unaffected by the low O2 conditions and were comparable to those of the open ocean. Sinking particles were composed of lithogenic particles of detrital origin and nonlithogenic particles of biogenic origin. Al, Ti, and Fe were mostly (at least 79%) lithogenic. About 75% of the Mn was nonlithogenic. Significant amounts (at least 58%) of Cu, Ba, Cd, and Mo were nonlithogenic.Sediment geochemistry varied across the continental shelf and slope. Cadmium, U, and Re have prominent maxima centered at 310 m, with 12.3 ppm, 10.9 ppm, and 68.3 ppb, respectively, at the core top. High values of Mo (averaging 6.8 ppm) and V (averaging 90 ppm) are seen in OMZ surface sediment. Additional down-core enrichment occurs for all redox-sensitive elements in the top 10 cm. For U, Mo, V, and Re, surface sediments are a poor indicator of metal enrichment. Comparison of the nonlithogenic composition of sediments with sinking particles suggests that direct input of plankton material enriched in metals makes a significant contribution to the total composition, especially for Cd, U, and Mo.We evaluated Re/Mo and Cd/U ratios as tracers for redox environments. Rhenium and Mo concentrations and Re/Mo ratios do not lead to consistent conclusions. Concurrent enrichments of Re and Mo are an indicator of an anoxic depositional environment. In contrast, high Re/Mo ratios are an indicator of suboxic conditions. Cadmium is enriched in surface sediments, while U has considerable down-core enrichment. The concentrations of Cd and U and the Cd/U ratio do not follow patterns predicted from thermodynamics. Though the water column is suboxic, these four redox-sensitive elements indicate that the sediments are anoxic. The implication for paleostudies is that a trace metal sediment signature that indicates anoxic conditions is not necessarily attributable to an anoxic water column.  相似文献   

17.
Down-core variations of granulometric, geochemical and mineral magnetism of a 70-cm long sediment core retrieved from the eastern Bay of Bengal abyssal region were studied to understand sedimentation pattern and sediment provenance during the last ~12 kyr BP. Based on down-core physical and elemental variations, three units were identified: unit 3 (70–43 cm) is a ~30 cm thick clayey silt organic carbon-rich (0.5–0.92%) turbidite probably delivered by the Brahmaputra River during the late Quaternary period. Units 2 (43–24 cm) and 1 (24–0 cm) represent enhanced and reduced supply of coarse-grained detrital sediments from the Ganges River during early and late Holocene period, respectively. Increased terrigenous supply dilutes calcium carbonate (CaCO3) and biogenic elements (P, Ba and Cu) in units 3 and 2. On the contrary, a reduction in detrital input enhances CaCO3 and biogenic elements in unit 1. Lithogenic elements (Ti, Al, K and Rb) and shale-normalized REE patterns in all three units suggest terrigenous source. The shift in provenance from the Brahmaputra to the Ganges derived sediments is evident by a sharp increase in sediment grain size, increased concentration and grain size assemblages of magnetic minerals, lithogenic elements concentration and Lan/Ybn ratio. This study highlights terrigenous dilution on biogenic sedimentation in the eastern Bay of Bengal sediments.  相似文献   

18.
通过对柴北缘地区的野外地质调查及室内实验分析,根据地质剖面中发育的岩石组合类型、沉积构造等特征,对研究区早奥陶世台地斜坡盆地相沉积体系进行了详细研究。认为研究区早古生代持续的海平面上升、柴北缘洋陆俯冲及陆弧碰撞是控制该时期盆山格局及沉积充填演化的重要因素。柴北缘早奥陶世台地边缘颗粒滩相发育在多泉山组中下部,岩性以生物碎屑灰岩、鲕粒灰岩以及泥晶灰岩为特征。而研究区斜坡相深水物质主要是由重力流搬运的碳酸盐岩再沉积物组成,共识别出包括细粒沉降微晶泥、滑塌角砾岩、颗粒流、瘤状灰岩、碎屑流以及浊积岩等不同类型的斜坡异地沉积物。研究区盆地相处于碳酸盐岩沉积体系岛弧碎屑岩沉积体系两大沉积体系的转换位置。受到柴北缘洋陆俯冲及陆弧碰撞等影响,隆升的陆壳基底及大陆岛弧物质向盆地提供大量碎屑物质,因此在靠近岛弧边缘地区发育了砂质碎屑流、浊流等重力流沉积体系下的弧后盆地沉积产物。  相似文献   

19.
The concentration of dissolved Ba in a number of rivers having their drainage almost entirely in Deccan Trap basalts has been measured. These results along with available data on the abundances of major elements in these waters, and on Ba and major elements in bed sediments of these rivers provide a measure of (i) the relative mobility of Ba during chemical weathering and erosion of basalts, particularly with respect to alkaline earths, Mg, Ca and Sr, and (ii) the flux of Ba out of the Deccan and its global significance. The concentration of dissolved Ba ranges from 8 to 105 nM. The average Ba/Mg*, Ba/Ca* and Ba/Sr (* is concentration corrected for atmospheric contribution) in waters is lower than the corresponding mean ratios in Deccan basalts, though they overlap within errors. Majority of the water samples, however, have ratios less than that in basalts. These findings can be interpreted as a cumulative effect of limited release/mobility of Ba during chemical weathering and erosion of basalts and its reactive behaviour in waters which promote its association with clays and oxy-hydroxides of Fe. These results also indicate that during chemical erosion of Deccan basalts, Ba is the least mobile among the alkaline earth elements. The abundance of Ba in sediments and their Ba/Al ratios relative to basalts are consistent with the above conclusion. Ba/Mg and Ba/Ca ratios in water and in sediments from the same location are strongly correlated; however, the mean ratios in waters are far less than those in sediments. This is a result of limited Ba mobility, effectively 5–6 times lower than that of Mg. The annual flux of dissolved Ba out of the Deccan Traps is ~1 × 107 moles, ~ 0.2% of its global riverine transport to oceans. The contribution of dissolved Ba from Deccan Traps, seem lower than its aerial coverage, ~ 0.5% of the global drainage area; the potential causes for this could be the lower abundance of Ba in basalts relative to “average continental crust”, and its behaviour during chemical weathering and erosion.  相似文献   

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