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Crystal-Size Dependence of Illite-Smectite Isotope Equilibration with Changing Fluids

Published online by Cambridge University Press:  01 January 2024

Lynda B. Williams*
Affiliation:
Department of Geological Sciences, Arizona State University, Tempe, Arizona 85287-1704, USA
Richard L. Hervig
Affiliation:
Department of Geological Sciences, Arizona State University, Tempe, Arizona 85287-1704, USA
*
*E-mail address of corresponding author: [email protected]
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Abstract

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Differences in equilibration rates among crystals of different sizes may be used to deduce paleofluid changes over time if the crystal-growth mechanism is known. To explore isotopic equilibration rates as a function of illite growth, we studied B-isotope changes during illitization of smectite. Montmorillonite (<2.0 µm SWy-1, K saturated) was reacted with aqueous boric acid (1000 ppm B) at 300°C, 100 MPa in sealed Au capsules (1:1 fluid:mineral ratio). The initial fluid was 0‰ (NBS 951 standard) but after R1 ordering occurred (65 days of reaction) the fluid was changed to −7‰ in order to examine the rate of isotopic re-equilibration. Samples were taken intermittently throughout the experiment. Each aliquot was NH4 exchanged and size separated into fine (<0.2 µm), medium (0.2–2.0 µm) and coarse (>2.0 µm) fractions. The isotopic composition of B in the tetrahedral sheet was then measured for comparison with the predicted equilibrium values.

The fine fraction showed equilibrium isotope ratios within 10 days, indicating that small, newly nucleated crystals precipitate in equilibrium with the fluid under supersaturated, closed conditions. These fine-fraction minerals did not re-equilibrate when the fluid was changed. The medium fraction gradually equilibrated with the initial fluid as illite grew to values >50%, but did not re-equilibrate with the later fluid. The coarse fraction was slow to begin recrystallization, perhaps due to dissolution kinetics of large crystals or the presence of detrital contaminants. However, it showed the fastest rate of isotopic change with crystal growth after R1 ordering. We conclude that at 300°C, the initial B–O bonds formed in illite are stable, and isotopic re-equilibration only occurs on new crystal growth. Therefore, different isotope ratios are preserved in different crystal size fractions due to different rates of crystal growth. Large crystals may reflect equilibrium with recent fluid while smaller crystals may retain isotope compositions reflecting equilibrium with earlier fluids.

Type
Research Article
Copyright
Copyright © 2006, The Clay Minerals Society

References

Bove, D.J. Eberl, D.D. McCarty, D.K. and Meeker, G.P., (2002) Characterization and modeling of illite crystal particles and growth mechanisms in a zoned hydrothermal deposit, Lake City, Colorado American Mineralogist 87 15461556 10.2138/am-2002-11-1204.CrossRefGoogle Scholar
Brime, C. and Eberl, D.D., (2002) Growth mechanisms of low-grade illites based on shapes of crystal thickness distributions Swiss Bulletin of Mineralogy and Petrology 82 203209.Google Scholar
Clauer, N. Środoń, J. Franců, J. and Šuchá, V., (1997) K-Ar dating of illite fundamental particles separated from illite-smectite Clay Minerals 32 181196 10.1180/claymin.1997.032.2.02.CrossRefGoogle Scholar
Clauer, N. Rinckenback, T. Weber, F. Sommer, F. Chaudhuri, S. and O’Neil, J.R., (1999) Diagenetic evolution of clay minerals in oil-bearing Neogene sandstones and associated shales from Mahakam Delta Basin (Kalimantan, Indonesia) American Association of Petroleum Geologists Bulletin 83 6287.Google Scholar
Clauer, N. Liewig, N. Pierret, M.-C. and Toulkeridis, T., (2003) Crystallization conditions of fundamental particles from mixed-layer illite-smectite of bentonites based on isotopic data (K-Ar, Rb-Sr and δ18O) Clays and Clay Minerals 51 664674 10.1346/CCMN.2003.0510609.CrossRefGoogle Scholar
Drits, V.A. Sakharov, B.A. Dainyak, L.G. Salyn, A.L. and Lindgreen, H., (2002) Structural and chemical heterogeneity of illite-smectites from Upper Jurassic mudstones of east Greenland related to volcanic and weathered parent rocks American Mineralogist 87 15901607 10.2138/am-2002-11-1209.CrossRefGoogle Scholar
Eberl, D.D. Whitney, G. and Khoury, H., (1978) Hydrothermal reactivity of smectite American Mineralogist 63 401409.Google Scholar
Eberl, D.D., Drits, V.A., Środoń, J. and Nüesch, R. (1996) MUDMASTER: a program for calculating crystallite size distributions and strain from the shapes of X-ray diffraction peaks. US Geological Survey Open File Report 96171.CrossRefGoogle Scholar
Eberl, D.D. Drits, V.A. and Środoń, J., (1998) Deducing the growth mechanisms of minerals from the shapes of crystal size distributions American Journal of Science 298 499533 10.2475/ajs.298.6.499.CrossRefGoogle Scholar
Eberl, D.D. Nüesch, Šuchá, V. and Tsipursky, S., (1998) Measurement of fundamental illite particle thicknesses by X-ray diffraction using PVP-10 intercalation Clays and Clay Minerals 46 8997 10.1346/CCMN.1998.0460110.CrossRefGoogle Scholar
Eberl, D.D., Drits, V.A. and Środoń, J. (2000) User’s guide to GALOPER — a program for simulating the shapes of crystal size distributions. US Geological Survey Open File Report 00505.Google Scholar
Eberl, D.D. Kile, D.E. and Drits, V.A., (2002) On geological interpretations of crystal size distributions: constant versus proportionate growth American Mineralogist 87 12351241 10.2138/am-2002-8-923.CrossRefGoogle Scholar
Elliott, W.C. Aronson, J.L. Matisoff, G. and Gautier, D.L., (1991) Kinetics of the smectite to illite transformation in the Denver Basin: Clay mineral, K-Ar data and mathematical model results American Association of Petroleum Geologists Bulletin 75 436462.Google Scholar
Girard, J.-P. and Savin, S.M., (1996) Intracrystalline fractionation of oxygen isotopes between hydroxyl and non-hydroxyl sites in kaolinite measured by thermal dehydroxylation and partial fluorination Geochimica et Cosmochimica Acta 60 469487 10.1016/0016-7037(95)00421-1.CrossRefGoogle Scholar
Güven, N. and Huang, W.-L., (1991) Effects of octahedral Mg2+ and Fe3+ substitutions on hydrothermal illitization reactions Clays and Clay Minerals 39 387399 10.1346/CCMN.1991.0390408.CrossRefGoogle Scholar
Hemming, N.G. and Hanson, G.N., (1992) Boron isotopic composition and concentration in modern marine carbonates Geochimica et Cosmochimica Acta 56 537543 10.1016/0016-7037(92)90151-8.CrossRefGoogle Scholar
Hervig, R.L., Grew, E.S. and Anovitz, L.M., (1996) Analyses of geological materials for boron by secondary ion mass spectrometry Boron Mineralogy, Petrology and Geochemistry Washington, D.C Mineralogical Society of America 789803 10.1515/9781501509223-018.CrossRefGoogle Scholar
Hervig, R.L. Moore, G.M. Williams, L.B. Peacock, S.M. Holloway, J.R. and Roggensack, K.R., (2002) Isotopic and elemental partitioning of boron between hydrous fluid and silicate melt American Mineralogist 87 769774 10.2138/am-2002-5-620.CrossRefGoogle Scholar
Hingston, F.J., (1964) Reactions between boron and clays Australian Journal of Soil Research 2 8395 10.1071/SR9640083.CrossRefGoogle Scholar
Kapteyn, J.C., (1903) Skew Frequency Curves in Biology and Statistics Groningen, The Netherlands Noordhoff Astronomical Laboratory 69 pp.Google Scholar
Kile, D. and Eberl, D.D., (2003) On the origin of size-dependent and size-independent crystal growth: Influence of advection and diffusion American Mineralogist 88 15141521 10.2138/am-2003-1014.CrossRefGoogle Scholar
Long, J.V.P., Potts, P.J. Bowles, J.F.W. Reed, S.J.B. and Cave, M.R., (1995) Microanalysis from 1950 to the 1990s Microprobe Techniques in the Earth Sciences London Chapman & Hall 148.Google Scholar
Marumo, K. Longstaffe, F.J. and Matsubaya, O., (1995) Stable isotope geochemistry of clay minerals from fossil and active hydrothermal systems, southwestern Hokkaido, Japan Geochimica et Cosmochimica Acta 59 25452559 10.1016/0016-7037(95)00149-2.CrossRefGoogle Scholar
Moore, D.M. and Reynolds, R.C., (1997) X-ray Diffraction and the Identification and Analysis of Clay Minerals 2 New York Oxford University Press 378 pp.Google Scholar
Mystkowski, K. Środoń, J. and Elsass, F., (2000) Mean thickness and thickness distribution of smectite crystallites Clay Minerals 35 545557 10.1180/000985500547016.CrossRefGoogle Scholar
Palmer, M.R. Swihart, G.H., Grew, E.S. and Anovitz, L.M., (1996) Boron isotope geochemistry: an overview Boron Mineralogy, Petrology and Geochemistry Washington, D.C Mineralogical Society of America 709744 10.1515/9781501509223-015.CrossRefGoogle Scholar
Pevear, D.R., Kharaka, Y.K. and Maest, A.S., (1992) Illite age analysis, a new tool for basin thermal analysis Water-Rock Interaction Rotterdam, The Netherlands Balkema 12511254.Google Scholar
Roberson, H.E. and Lahann, R.W., (1981) Smectite to illite conversion rates; Effects of solution chemistry Clays and Clay Minerals 29 129135 10.1346/CCMN.1981.0290207.CrossRefGoogle Scholar
Savin, S.M. Lee, M. and Bailey, S.W., (1988) Isotopic studies of phyllosilicates Hydrous Phyllosilicates (Exclusive of Micas) Washington, D.C Mineralogical Society of America 189223 10.1515/9781501508998-012.CrossRefGoogle Scholar
Sheppard, S.M.F. and Gilg, H.A., (1996) The stable isotope geochemistry of clay minerals Clay Minerals 31 124 10.1180/claymin.1996.031.1.01.CrossRefGoogle Scholar
Środoń, J. and Clauer, N., (2001) Diagenetic history of Lower Palaeozoic sediments in Pomerania (northern Poland), traced across the Teisseyre-Tornquist tectonic zone using mixed-layer illite/smectite Clay Minerals 36 1527 10.1180/000985501547321.CrossRefGoogle Scholar
Środoń, J. Eberl, D.D. and Drits, V.A., (2000) Evolution of fundamental particle size during illitization of smectite and implications for reaction mechanism Clays and Clay Minerals 48 446458 10.1346/CCMN.2000.0480405.CrossRefGoogle Scholar
Tonarini, S. Pennisi, M. and Leeman, W.P., (1997) Precise boron isotopic analysis of complex silicate (rock) samples using alkali carbonate fusion and ion-exchange separation Chemical Geology 142 129137 10.1016/S0009-2541(97)00087-9.CrossRefGoogle Scholar
Whitney, G. and Northrup, H.R., (1988) Experimental investigation of the smectite to illite reaction: Dual reaction mechanisms and oxygen-isotope systematics American Mineralogist 73 7790.Google Scholar
Williams, L.B., (2000) Boron isotope geochemistry during burial diagenesis Alberta, Canada University of Calgary 168 pp.Google Scholar
Williams, L.B. and Hervig, R.L., (2002) Intracrystalline boron isotope variations in clay minerals: a potential low-temperature single mineral geothermometer American Mineralogist 87 15641570 10.2138/am-2002-11-1206.CrossRefGoogle Scholar
Williams, L.B. and Hervig, R.L., (2005) Lithium and boron isotopes in illite-smectite: The importance of crystal size Geochimica et Cosmochimica Acta 69 57055716 10.1016/j.gca.2005.08.005.CrossRefGoogle Scholar
Williams, L.B. Hervig, R.L. Holloway, J.R. and Hutcheon, I., (2001) Boron isotope geochemistry during diagenesis: Part 1. Experimental determination of fractionation during illitization of smectite Geochimica et Cosmochimica Acta 65 17691782 10.1016/S0016-7037(01)00557-9.CrossRefGoogle Scholar
Zhang, L. Chan, L.H. and Gieskes, J.M., (1998) Lithium isotope geochemistry of pore waters from Ocean Drilling Program Sites 918 and 919, Irminger Basin Geochimica et Cosmochimica Acta 62 24372450 10.1016/S0016-7037(98)00178-1.CrossRefGoogle Scholar