Approaches to equilibrium in the distribution of trace elements among the principal minerals in a high-grade metamorphic terrane

Citation
R. Kretz et al., Approaches to equilibrium in the distribution of trace elements among the principal minerals in a high-grade metamorphic terrane, J METAMORPH, 17(1), 1999, pp. 41-59
Citations number
50
Categorie Soggetti
Earth Sciences
Journal title
JOURNAL OF METAMORPHIC GEOLOGY
ISSN journal
02634929 → ACNP
Volume
17
Issue
1
Year of publication
1999
Pages
41 - 59
Database
ISI
SICI code
0263-4929(199901)17:1<41:ATEITD>2.0.ZU;2-U
Abstract
X-ray fluorescence, instrumental neutron activation, and particle-induced X -ray emission methods were used to determine the distribution of numerous t race elements among garnet (Grt), Ca-pyroxene (Cpx), hornblende (Hbl), biot ite (Bt), plagioclase (Pl) and K-feldspar (Kf) in a high-grade metamorphic terrane within the Grenville Province of the Canadian Shield. Results are p resented as distribution formulae, e.g. Sr: Kf 1.1 Pl 16 Hbl 2.2 Cpx 1.0 Pt 1.2 Grt Sc: Hbl 1.1 Cpx 1.0 Crt 7.8 Bt 22 Pl 2.6 Kf V: Hbl 1.15 Bt 2.07 Cpx 6.0 Crt (1.4% CaO) > l (Pl, Kf) Zn: Bt 1.6 Hbl 1.62 Cpx 2.9 Grt 10 Pl Ga: Bt 1.2 Hbl 1.2 Pl 2.5 Cpx 1.3 Grt where numbers are distribution ratios, e.g. ppm Sr in Hbl/ppm Sr in Cpx = 2 .2. Examples of inter-element similarities and differences are (a) both Rb and Cs are concentrated in biotite relative to K-feldspar, but for Rb the r atio is 2.3 and for Cs it is 16, (b) the distribution formulae for seven la nthanides are similar except for the position of garnet, e.g. Ce: Hbl 2.7 Cpx 2.8 Pl 1.1 Bt 11 Kf 16 Grt Yb: Grt 2.8 Hbl 2.7 Cpx 9 Pl 1.0 Bt 7 Kf and (c) all of Sr, eight lanthanides, Zr, V and Cr are concentrated in horn blende relative to Ca-pyroxene by a factor that lies in the narrow range of 2.2-3.1. There is a larger variation (departure from the mean) in some dis tribution ratios than in others. Thus the mean ratios (Hbl/Cpx) for each of six elements and in parentheses the percentage relative standard deviation are Zn 1.62 (8.6), V 2.38 (12), Cr 2.42 (18), Sr 2.7 (28), Pa 2.9 (36) and Ni 1.66 (38). We suggest that variation of this kind is the result of diff erences from place to place in the magnitude of deformation and recrystalli zation (which facilitated the rearrangement of atoms), combined with rates of lattice and crystal-boundary diffusion that are unique for the various e lements, thus permitting some trace elements to approach equilibrium more c losely than others.