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碳酸盐岩风化过程中的U-Th不平衡研究-以黔中、黔北为例
其他题名U-Th disequilibria in the Weathering-pedogenic processes of carbonate rocks: exemplified by two profiles in central and northern Guizhou Province
于晓红
2008-06-06
学位授予单位中国科学院地球化学研究所
学位授予地点地球化学研究所
学位名称博士
关键词碳酸盐岩 风化 u Th 不平衡
摘要为了进一步获得贵州碳酸盐岩风化成土过程的信息,为测定风化成土速率的研究工作奠定基础,本次研究工作通过U-Th的地球化学特征与主量元素、微量元素、稀土元素的地球化学特征的对比研究以及U-Th不平衡来研究贵州两个碳酸盐岩风化剖面的风化成土过程,并得出以下总体认识: 贵州碳酸盐岩风化剖面中的238U-234U-230Th不平衡说明风化剖面中的U-Th不平衡与风化过程密切相关,与风化壳中矿物和铁壳的演化特征密切相关。风化剖面不仅被简单的持续积累或者滤失过程所控制,而且被每一个土层中的复杂的重组过程所影响。U-Th不平衡也说明风化系统的扰动可能与中更新世晚期的气候变化有关。风化剖面中的U-Th不平衡是由母岩碳酸盐岩的风化、风化流体的溶解作用、表土层中的有机质、铁质结核带中的氧化铁矿物以及伊利石、高岭石等粘土矿物对U、Th的吸附作用、α反冲作用以及微生物的还原作用等共同作用的结果。 具体结论如下: (1)两个风化剖面中的U、Th都在半风化层中相对基岩强烈富集,安顺白云岩风化剖面中U、Th在全风化层中下部富集;而遵义石灰岩风化剖面中的U在全风化层中部富集,Th在全风化层上部富集,然后向表土层逐渐减少。 (2)U、Th在半风化层中相对基岩强烈富集,是因为在半风化层中,基岩中的原生矿物发生溶解、蚀变,生成新的次生粘土矿物伊利石,而伊利石对U、Th具有强烈的吸附能力。风化剖面中U、Th的富集主要与地表水的淋滤作用以及铁壳在进一步的风化过程中溶解释放出其中所富集的U、Th,而U、Th向下重新迁移的过程有关。 (3)风化剖面中U、Th的分布特征说明U、Th的含量与风化过程密切相关,与风化壳中的矿物和铁壳的演化特征密切相关。遵义石灰岩风化剖面中U、Th的淋失程度比安顺白云岩风化剖面中U、Th的淋失程度弱也说明了遵义石灰岩风化剖面的风化程度要低于安顺白云岩风化剖面的风化程度。 (4)安顺白云岩风化剖面中,234U/238U在<1和>1之间交替变化。除在剖面中部,230Th/238U≈1外,230Th/238U基本上都>1。 (5)安顺白云岩风化剖面中的238U -234U-230Th不平衡表明:安顺白云岩风化剖面中的U-Th不平衡是母岩碳酸盐岩的风化、风化流体的溶解作用、表土层中的有机质、铁质结核带中的氧化铁矿物以及伊利石、高岭石等粘土矿物对234U、230Th的吸附作用、α反冲作用以及微生物的还原作用等共同作用的结果。 (6)遵义石灰岩风化剖面中234U/238U除少数几个点外,大多数采样点的234U/238U都<1。除了少数几个点外,大部分230Th/238U>1。 (7)遵义石灰岩风化剖面中的238U -234U-230Th不平衡表明:234U-238U不平衡主要是由地表水和入渗水的溶解作用以及α反冲作用为主要的控制机制。而风化剖面中230Th-238U不平衡主要是由表土层中的有机质、高岭石、氧化铁矿物以及伊利石对230Th吸附作用和α反冲作用共同作用的结果。 (8)将U的迁移模型应用于本研究中的两个碳酸盐岩风化剖面,说明这两个风化剖面都被U的近期积累或者滤失过程所影响,风化系统处于过渡的不稳定状态,并通过U在风化剖面中的重新迁移将系统带回稳定状态。 (9)由等时线定年法计算出的安顺白云岩风化剖面的年龄范围为:87.0±7.8-479.2±47.9ka;遵义石灰岩风化剖面的年龄范围为:62.3±8.7-353.3±31.8ka。 (10)由等时线定年法可知:两个风化系统将在~1.1Ma达到稳定状态。 (11)碳酸盐岩风化剖面应用U的迁移模型得出的U的迁移过程与风化剖面中主量元素和微量元素的迁移特征相吻合,说明模型的选择是正确的。 (12)整个风化剖面的238U-234U-230Th不平衡说明风化剖面中的U-Th不平衡与风化过程密切相关,与风化壳中矿物和铁壳的演化特征密切相关。风化系统的扰动可能与中更新世晚期的气候变化有关。碳酸盐岩风化剖面被U的近期迁移过程所影响,风化剖面中的每一个单元甚至每一个土样都具有复杂的历史。这些单元或者土样是古老的风化历史和近期的重新迁移过程的叠加。
其他摘要In order to obtain more information about the weathering-pedogenic processes of carbonate rocks in Guizhou, Province and lay the foundation for the future research in determining the rate of weathering-pedogenesis, the weathering-pedogenic processes of two profiles of carbonate rocks from Guizhou Province has been studied in this research, by comparing the geochemical characteristics of uranium and thorium to that of major elements, trace elements and rare earth elements and the study of the U-Th disequilibria. The general conclusions are summarized as follows: The 238U-234U-230Th disequilibria of the weathering profiles of carbonate rocks from Guizhou Province indicated that the U-Th disequilibria correlated to the weathering processes and to the evolution characteristics of minerals and ferruginous caps in the weathering profiles tightly. The weathering profiles were affected not only by the simple accumulating or leaching processes but also by the complex reorganization within each horizon. The U-Th disequilibria also suggested that the perturbation of the systems could correspond to the late middle Pleistocene climatic variations.The U-Th disequilibria in the weathering profiles of the carbonate rocks were caused by the weathering of parent carbonate rocks, the dissolving of uranium by the weathering liquids, the adsorption capacity of the organic matters, ferruginous oxides and clay minerals such as illite, kaolinite to uranium and thorium in the surface soil zone, the ferrous bands and the moderately weathered zone, respectively. They were also caused by α-recoil and the reduction of microorganism. And the detailed conclusions are as follows: (1) Comparing to the bedrock, uranium and thorium in the two profiles were strongly accumulated in the moderately weathered zone. Uranium and thorium in the Anshun dolomite profile accumulated in the lower part of the completely weathered zone. While the uranium accumulated in the middle of the completely weathered zone and thorium accumulated in the upper of the completely weathered zone in the Zunyi limestone profile. Then they decreased gradually to the top of the profile. (2) Comparing to the bedrock, uranium and thorium in the two profiles were strongly accumulated in the moderately weathered zone. The reason is that during the weathering processes, the primary minerals in the bedrock dissolving, eroded and formed new secondary clay minerals, i.e. illite. The affinity of illite to uranium and thorium is strong. The accumulation of uranium and thorium in the weathering profiles resulted from the eluviation of surface water and the further weathering of ferruginous caps. The dissolving of ferruginous caps released the adsorbed uranium and thorium, the downward remobilization of uranium and thorium also made them accumulate in the middle and bottom of the completely weathered zone. (3) The distribution characteristics of uranium and thorium in the weathering profiles suggested that the content of uranium and thorium correlated to the weathering processes and to the evolution characteristics of minerals and ferruginous caps in the weathering profiles tightly. The leaching degree of uranium and thorium in the Zunyi limestone profile is lower than that of Anshun dolomite profile indicted that the weathering degree of Zunyi limestone profile is lower than that of Anshun dolomite profile. (4) Most of the 234U/238U activity ratio in the Anshun dolomite profile changed between <1 and >1. Except in the middle of the profile, 230Th/238U≈1, almost all of 230Th/238U are higher than 1. (5) The 238U -234U-230Th disequilibria in the Anshun dolomite profile suggested that the 238U -234U-230Th disequilibria in the weathering profile were caused by the weathering of parent carbonate rocks, the dissolving of uranium by the weathering liquids, the adsorption capacity of the organic matters, ferruginous oxides and clay minerals such as illite, kaolinite to uranium and thorium in the surface soil zone, the ferrous bands and the moderately weathered zone, respectively. They were also caused by α-recoil and the reduction of microorganism. (6) Except few sampling points, 234U/238U in most sampling points of Zunyi limestone profile are lower than 1, and 230Th/238U in most sampling points are higher than 1. (7) The 238U -234U-230Th disequilibria in the Zunyi limestone profile suggested that the 234U-238U disequilibrium were mainly caused by the dissolving of uranium by surface water and the infiltration water and α recoil. While the 230Th-238U disequilibrium were mainly caused by the adsorption of organic matters in the surface soil zone, kaolinite, ferruginous oxides and illite to thorium and α recoil. (8) In this study, application of the modeling of U mobility to the weathering profiles of the carbonate rocks suggested that these two profiles were all affected by the recent accumulating or leaching processes of uranium. The weathering systems were not in steady states but transient states. The uranium remobilization could bring the systems back to steady states. (9) Calculated with the isochrone dating method, the age ranges of Anshun dolomite profile are from 87.0±7.8 ka to 479.2±47.9ka and that of Zunyi limestone are from 62.3±8.7 ka to 353.3±31.8ka. (10) From the isochrone dating method, we know that the steady state of the two weathering systems will be reached in 1.1Ma. (11) The mobility processes of uranium in the weathering profiles of carbonate rocks which were inferred from the modeling of U mobility is consistent with the mobility processes of major elements and trace elements suggested that the selection of the model is correct. (12) The 238U-234U-230Th disequilibria of the whole weathering profiles suggested that the perturbation of the systems could correspond to the late middle Pleistocene climatic variations. The weathering profiles of carbonate rocks are affected by remobilization processes of uranium. In summary, each unit, and even each sample, has a complex history with superimposition of old formation steps and further remobilization processes.
页数143
语种中文
文献类型学位论文
条目标识符http://ir.gyig.ac.cn/handle/352002/3398
专题研究生_研究生_学位论文
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于晓红. 碳酸盐岩风化过程中的U-Th不平衡研究-以黔中、黔北为例[D]. 地球化学研究所. 中国科学院地球化学研究所,2008.
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