How does Chinese loess become magnetized?
How does Chinese loess become magnetized?
Despite nearly three decades of paleomagnetic research on the extensive Chinese loess deposits, a convincing explanation has yet to be developed for how Chinese loess becomes magnetized. To address this problem, we conducted re-deposition experiments using weakly consolidated Holocene Chinese loess that was disaggregated in the laboratory, and compare our results with published paleomagnetic data. We simulated a depositional remanent magnetization (DRM) associated with dry deposition of eolian sediments, and a post-depositional remanent magnetization (PDRM) in which the sediment was water-saturated after deposition. The simulated DRM faithfully records the declination of the applied field, but with systematic inclination flattening. Addition of minor water slightly improves recording of the applied field, but inclination flattening persists. Reliable recording of the applied field occurs for PDRM simulation in water-saturated sediment. Our synthesis of paleomagnetic data from Chinese loess indicates that time-averaged paleomagnetic directions are often indistinguishable from the expected geocentric axial dipole (GAD) field, but in many cases inclinations are shallower than for a GAD field. We conclude that the Chinese loess is magnetized by a combination of DRM and PDRM mechanisms, with water content providing the dominant control on which mechanism aligns the detrital mineral fraction. Where pedogenesis causes neoformation of magnetic minerals, an additional chemical remanent magnetization (CRM) will occur. The magnetization of Chinese loess therefore appears to be controlled by a complex time-varying combination of DRM, PDRM and CRM mechanisms.
112-122
Zhao, Xiang
99ee573a-4607-40b5-a473-2046d623a2e0
Roberts, Andrew P.
4f062491-5408-4edb-8dd1-140c6a42e93f
15 March 2010
Zhao, Xiang
99ee573a-4607-40b5-a473-2046d623a2e0
Roberts, Andrew P.
4f062491-5408-4edb-8dd1-140c6a42e93f
Zhao, Xiang and Roberts, Andrew P.
(2010)
How does Chinese loess become magnetized?
Earth and Planetary Science Letters, 292 (1-2), .
(doi:10.1016/j.epsl.2010.01.026).
Abstract
Despite nearly three decades of paleomagnetic research on the extensive Chinese loess deposits, a convincing explanation has yet to be developed for how Chinese loess becomes magnetized. To address this problem, we conducted re-deposition experiments using weakly consolidated Holocene Chinese loess that was disaggregated in the laboratory, and compare our results with published paleomagnetic data. We simulated a depositional remanent magnetization (DRM) associated with dry deposition of eolian sediments, and a post-depositional remanent magnetization (PDRM) in which the sediment was water-saturated after deposition. The simulated DRM faithfully records the declination of the applied field, but with systematic inclination flattening. Addition of minor water slightly improves recording of the applied field, but inclination flattening persists. Reliable recording of the applied field occurs for PDRM simulation in water-saturated sediment. Our synthesis of paleomagnetic data from Chinese loess indicates that time-averaged paleomagnetic directions are often indistinguishable from the expected geocentric axial dipole (GAD) field, but in many cases inclinations are shallower than for a GAD field. We conclude that the Chinese loess is magnetized by a combination of DRM and PDRM mechanisms, with water content providing the dominant control on which mechanism aligns the detrital mineral fraction. Where pedogenesis causes neoformation of magnetic minerals, an additional chemical remanent magnetization (CRM) will occur. The magnetization of Chinese loess therefore appears to be controlled by a complex time-varying combination of DRM, PDRM and CRM mechanisms.
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Published date: 15 March 2010
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Local EPrints ID: 79481
URI: http://eprints.soton.ac.uk/id/eprint/79481
ISSN: 0012-821X
PURE UUID: 36fb6f1e-2361-4bf7-8c0c-a45446dfda54
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Date deposited: 16 Mar 2010
Last modified: 14 Mar 2024 00:30
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Author:
Xiang Zhao
Author:
Andrew P. Roberts
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