Hostname: page-component-7479d7b7d-jwnkl Total loading time: 0 Render date: 2024-07-11T14:13:09.917Z Has data issue: false hasContentIssue false

Hydrothermal Regularly Interstratified Chlorite-Vermiculite and Tobermorite in Alteration Zones at Goldfield, Nevada

Published online by Cambridge University Press:  01 January 2024

Richard D. Harvey*
Affiliation:
Department of Geology, Indiana University, Bloomington, Indiana, USA
Carl W. Beck
Affiliation:
Department of Geology, Indiana University, Bloomington, Indiana, USA
*
1Present address: Illinois Geological Survey, Urbana, Illinois.

Abstract

Hydrothermal alteration of andesitic and dacitic rocks in the Goldfield District, Nevada, has produced regularly interstratified chlorite-vermiculite and tobermorite. X-ray diffraction and oscillating-heating data indicate the regular interstratification of the chlorite-vermiculite. This mineral is found in the zone of least alteration and was formed by the alteration of hornblende phenocrysts. Penninite is an intermediate stage in this reaction. Increased intensity of alteration resulted in the disappearance of chlorite-vermiculite and the development of montmorillonite. Tobermorite, found only in the dacite, is associated with alunite as pseudomorphs after plagioclase phenocrysts in the most intense zone of alteration. The intermediate stage of hydration for tobermorite is indicated by the 11 Å spacing of the 002 diffraction peak. Oscillating-heating X-ray data at atmospheric pressure show that tobermorite decomposes thermally in two stages. The (00l) planes collapse at approximately 520 °C and crystal planes having an 8 Å periodicity collapse at about 760 °C. Wollastonite develops from tobermorite above 700 °C under static heating conditions.

Type
General Session
Copyright
Copyright © The Clay Minerals Society 1960

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bradley, W. F. and Weaver, C. E. (1956) A regularly interstratified chlorite-vermiculite clay mineral: Amer. Min., v. 41, pp. 497504.Google Scholar
Brindley, G. W. and Ali, S. Z. (1950) X-ray study of thermal transformations in some magnesian chlorite minerals. Acta Cryst., v. 3, pp. 2530.CrossRefGoogle Scholar
Claringbull, G. F. and Hey, M. H. (1952) A re-examination of tobermorite: Min. Mag., v. 29, pp. 960962.Google Scholar
Eakle, A. S. (1917) Minerals associated with the crystalline limestone at Crestmore, Riverside County, California: Calif. Univ., Dept. of Geol. Bull. 10, pp. 327360.Google Scholar
Gard, J. A. and Taylor, H. F. W. (1957) A further investigation of tobermorite from Loch Eynort, Scotland: Min. Mag., v. 31, pp. 361370.Google Scholar
Heddle, M. F. (1880) Preliminary notice of substances which may prove to be new minerals: Min. Mag., v. 4, pp. 117123.Google Scholar
Kerr, P. F. (1959) Optical Mineralogy. McGraw-Hill Book Co., Inc., New York, 3rd ed., 442 pp.Google Scholar
McConnell, J. D. C. (1954) The hydrated calcium silicates riversideite, tobermorite and plombierite: Min. Mag., v. 30, pp. 293305.Google Scholar
Megaw, H. D. and Kelsey, C. H. (1956) The crystal structure of tobermorite: Nature, v. 177, pp. 390393.CrossRefGoogle Scholar
Ransome, F. L. (1909) The geology and ore deposits of Goldfield, Nevada: U.S. Geol. Survey, Prof. Paper 66, 258 pp.Google Scholar
Searls, F. Jr. (1948) A contribution to the published information on the geology and ore deposits of Goldfield, Nevada: Univ. Nevada Bull. no. 5, v. 42, Geol. and Min. series no. 48, p. 24.Google Scholar
Taylor, H. F. W. (1959) The dehydration of tobermorite: in Clays and Clay Minerals, Pergamon Press, New York, v. 6, pp. 101109.Google Scholar
Taylor, H. F. W. and Howison, J. W. (1956) Relationships between calcium silicates and clay minerals: Clay Min. Bull., v. 3, pp. 98111.CrossRefGoogle Scholar
Weiss, E. J. and Rowland, R. A. (1956) Oscillating-heating X-ray diffractometer studies of clay mineral dehydroxylation: Amer. Min., v. 41, pp. 117126.Google Scholar