Knowledge Resource Center for Ecological Environment in Arid Area
DOI | 10.1016/j.chemgeo.2002.06.001 |
Halloysite as a kinetically controlled end product of arid-zone basalt weathering | |
Ziegler, K; Hsieh, JCC; Chadwick, OA; Kelly, EF; Hendricks, DM; Savin, SM | |
通讯作者 | Ziegler, K |
来源期刊 | CHEMICAL GEOLOGY
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ISSN | 0009-2541 |
出版年 | 2003 |
卷号 | 202期号:3-4页码:461-478 |
英文摘要 | Mineralogical and isotope results paired with field observations suggest that halloysite is the favored, albeit metastable, aluminosilicate end product of arid-zone basalt weathering on Kohala, Hawai’i, and that the formation of smectite has been inhibited by kinetic factors. Soils sampled on constructional lava flows having ages ranging from 4 to 350 ka provide a chronosequence that has had minimal physical disturbance, thus allowing us to interpret chemical and mineralogical changes as the result of a time-dependent process. The halloysite content of the soil increases with increasing soil age; its growth is at the expense of allophane, which, in turn, forms at the expense of primary minerals. These mineral relationships suggest that halloysite has been forming continuously throughout the lifetime of the soil. Smectite, the thermodynamically stable phyllosilicate phase predicted by soil solution composition, is not found in these and soils. We determined that our soil system is controlled by kinetic factors, and that, therefore, thermodynamic predictions do not reflect reality. The main factors favoring kinetic control of halloysite formation are intense, but short wet periods followed by prolonged extremely dry seasons, and microenvironmental conditions leading to immediate uptake of released Al by the halloysite-precursor mineral allophane. The delta(18)O relationship between present-day soil water and halloysite, formed over the last 170 ka, was used as a tracer of past soil conditions. Results from a reconstruction of paleo-climate and -soil conditions, combined with delta(18)O data, observed mineral relationships along the 350 ka chronosequence, and field evidence for long-term aridity rule out the possibility that the and side of Kohala was affected by prolonged periods of higher rainfall that could have produced more dilute soil waters and, therefore, altered mineralogical stabilities. We conclude that pedogenic halloysite has been continually forming from the early stage of soil formation, and that it has consistently formed under isotopic equilibrium conditions, indicating that halloysite delta(18)O compositions imply paleoclimatic conditions over the time of its formation that are similar to today’s. (C) 2003 Elsevier B.V. All rights reserved. |
英文关键词 | Hawai’i soil water climate oxygen isotopes kinetics |
类型 | Article ; Proceedings Paper |
语种 | 英语 |
国家 | USA |
收录类别 | CPCI-S ; SCI-E |
WOS记录号 | WOS:000187466800014 |
WOS关键词 | OXYGEN-ISOTOPE SYSTEMATICS ; CLAY-MINERALS ; VOLCANIC ASH ; FORMING PROCESSES ; STABLE-ISOTOPE ; SOIL-WATER ; GEOCHEMISTRY ; DEUTERIUM ; HYDROGEN ; HAWAII |
WOS类目 | Geochemistry & Geophysics |
WOS研究方向 | Geochemistry & Geophysics |
来源机构 | University of Arizona ; Colorado State University |
资源类型 | 期刊论文 |
条目标识符 | http://119.78.100.177/qdio/handle/2XILL650/144316 |
作者单位 | (1)Univ Calif Santa Barbara, Dept Geog, Santa Barbara, CA 93106 USA;(2)ChevronTexaco, Houston, TX 77042 USA;(3)Colorado State Univ, Dept Soil & Crop Sci, Ft Collins, CO 80523 USA;(4)Univ Arizona, Dept Soil Water & Environm Sci, Tucson, AZ 85721 USA;(5)Case Western Reserve Univ, Dept Geol Sci, Cleveland, OH 44106 USA |
推荐引用方式 GB/T 7714 | Ziegler, K,Hsieh, JCC,Chadwick, OA,et al. Halloysite as a kinetically controlled end product of arid-zone basalt weathering[J]. University of Arizona, Colorado State University,2003,202(3-4):461-478. |
APA | Ziegler, K,Hsieh, JCC,Chadwick, OA,Kelly, EF,Hendricks, DM,&Savin, SM.(2003).Halloysite as a kinetically controlled end product of arid-zone basalt weathering.CHEMICAL GEOLOGY,202(3-4),461-478. |
MLA | Ziegler, K,et al."Halloysite as a kinetically controlled end product of arid-zone basalt weathering".CHEMICAL GEOLOGY 202.3-4(2003):461-478. |
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