Mineral chemistry of gahnite from the Lalor metamorphosed VHMS deposit, Snow Lake, Manitoba

2020 ◽  
Vol 58 (4) ◽  
pp. 511-532
Author(s):  
Elliot A. Wehrle ◽  
Andrew M. McDonald ◽  
Douglas K. Tinkham

ABSTRACT Gahnite (ZnAl2O4) is a common accessory mineral at the Lalor auriferous Zn-Cu metamorphosed VHMS deposit (Snow Lake, Manitoba). To evaluate factors influencing its crystal chemistry, gahnite representing a range of textures, host mineral assemblages, and whole-rock compositions were analyzed for major, minor, and trace elements. The analyzed grains span the range of Ghn63-75Her15-22Spl10-18 and are un-zoned with respect to Zn, Fe, and Mg. A moderate positive correlation exists between Mg in gahnite and whole-rock MgO (R2 = 0.66). The minor- and trace-element chemistry of the Lalor gahnite is dominated by Mn (400–2600 ppm), Si (<25–250 ppm), and V (<25–2300 ppm). Based on the limited variability in gahnite major-element composition, as well as similar partitioning coefficients of Zn and Fe between sphalerite-gahnite pairs (indicating comparable metamorphic conditions of crystallization for the analyzed gahnite), metamorphic grade is interpreted to have had the strongest influence on gahnite major-element chemistry. Most sphalerite occurs with pyrite and pyrrhotite, an assemblage that would have buffered fS2 and fixed the Zn:Fe ratio in sphalerite, which also could have contributed to the narrow compositional range observed in gahnite. Magnesium was not an essential component of the sphalerite-consuming, gahnite-producing reactions, so its concentration in gahnite was more readily affected by whole-rock Mg. A small proportion of gahnite grains may have formed from the destabilization of silicates (staurolite and biotite), rather than sphalerite. These possible gahnite-forming reactions (sphalerite- versus biotite- or staurolite-consuming) appear to have had the strongest control on gahnite minor- and trace-element chemistry, as gahnite formed from sphalerite desulfidation reactions shows a range in Mn (450–2600 ppm) and restricted V/Mn values (<0.5), while gahnite interpreted to have formed from the dehydration of biotite and staurolite shows restricted Mn (<430 ppm) and a range of V/Mn values (0.75–5.5). Further work is recommended to investigate the possibility of using gahnite trace-element signatures (such as with Mn and V) to discriminate between gahnite that crystallized in sphalerite-rich and sphalerite-barren environments, as this concept has potential for application to exploration using detrital gahnite.

2018 ◽  
Author(s):  
Casey Beaudoin ◽  
◽  
G. Nelson Eby

The Holocene ◽  
2011 ◽  
Vol 21 (7) ◽  
pp. 1037-1048 ◽  
Author(s):  
Bergrún Arna Óladóttir ◽  
Olgeir Sigmarsson ◽  
Gudrún Larsen ◽  
Jean-Luc Devidal

The Holocene eruption history of subglacial volcanoes in Iceland is largely recorded by their tephra deposits. The numerous basaltic tephra offer the possibility to make the tephrochronology in the North Atlantic area more detailed and, therefore, more useful as a tool not only in volcanology but also in environmental and archaeological studies. The source of a tephra is established by mapping its distribution or inferred via compositional fingerprinting, mainly based on major-element analyses. In order to improve the provenance determinations for basaltic tephra produced at Grímsvötn, Bárdarbunga and Kverkfjöll volcanic systems in Iceland, 921 samples from soil profiles around the Vatnajökull ice-cap were analysed for major-element concentrations by electron probe microanalysis. These samples are shown to represent 747 primary tephra units. The tephra erupted within each of these volcanic system has similar chemical characteristics. The major-element results fall into three distinctive compositional groups, all of which show regular decrease of MgO with increasing K2O concentrations. The new analyses presented here considerably improve the compositional distinction between products of the three volcanic systems. Nevertheless, slight overlap of the compositional groups for each system still remains. In situ trace-element analyses by laser-ablation-inductively-coupled-plasma-mass-spectrometry were applied for better provenance identification for those tephra having similar major-element composition. Three trace-element ratios, Rb/Y, La/Yb and Sr/Th, proved particularly useful. Significantly higher La/Yb distinguishes the Grímsvötn basalts from those of Bárdarbunga and Rb/Y values differentiate the basalts of Grímsvötn and Kverkfjöll. Additionally, the products of Bárdarbunga, Grímsvötn and Kverkfjöll form distinct compositional fields on a Sr/Th versus Th plot. Taken together, the combined use of major- and trace-element analyses in delineating the provenance of basaltic tephra having similar major-element composition significantly improves the Holocene tephra record as well as the potential for correlations with tephra from outside Iceland.


1980 ◽  
Vol 43 (330) ◽  
pp. 765-770 ◽  
Author(s):  
A. M. Duncan ◽  
R. M. F. Preston

SummaryThe chemical variation of clinopyroxene phenocrysts from the trachybasaltic lavas of Etna volcano is described. The phenocrysts show a limited, but distinct trend in chemical variation from calcic-augite in the hawaiites to augite in the benmoreites. The trend of this variation is unusual, being one of Mg-enrichment with differentiation of the magma. Ca shows a steady decrease in the clinopyroxenes from the hawaiites to the benmoreites. Na, however, shows little chemical variation in the pyroxenes. The trace element chemistry is briefly examined. The clinopyroxenes show well-developed oscillatory and sector zoning. The basal {11} sectors are enriched in Si and Mg and depleted in Ti, Al, and Fe relative to the {100}, {110}, and {010} prism sectors.


1994 ◽  
Vol 62 (1-4) ◽  
pp. 429-452 ◽  
Author(s):  
Christopher J. Nye ◽  
Samuel E. Swanson ◽  
Victoria F. Avery ◽  
Thomas P. Miller

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