Mineral Chemistry and Reaction Textures of Calc-silicate Rocks of the Lunavada Region, SAMB, NE Gujarat

2021 ◽  
Vol 97 (2) ◽  
pp. 151-157
Author(s):  
Gayatri Akolkar ◽  
M. A. Limaye
2003 ◽  
Vol 67 (3) ◽  
pp. 423-451 ◽  
Author(s):  
E. A. Dunworth ◽  
K. Bell

AbstractThe Turiy Massif, on the southern coast of the Kola Peninsula, consists of five intrusive complexes containing a variety of carbonatites, phoscorites, melilitolites, ijolites and pyroxenites. Petrographic and mineralogical studies of the different rocks show that the samples are texturally heterogeneous. Minerals including apatite, garnet, magnetite, melilite, mica and pyroxene, show systematic variations in composition relating to the rock type in which they occur. Compositional similarities and/or distinct trends are seen in the mineral compositions within the each of the pyroxenite-melilitolite, and melteigite-ijolite rock series, indicating linked petrogenetic histories within each of the two series. The carbonatites from the northern complex may be related to nearby melilitolites, but the central complex carbonatites and phosocorites do not bear any mineralogical (or isotopic) similarities to any of the silicate rocks within the massif.


Author(s):  
Chris Harris ◽  
Lucrecia Maboane

ABSTRACT The Garies wollastonite deposit is located in the Bushmanland terrane of the Namaqualand Metamorphic Province and is part of a discontinuous calc-silicate unit bounded by granulite facies gneiss that experienced peak metamorphic temperatures above 800 °C. In bulk, the deposit is dominated by wollastonite, but varied proportions of garnet, diopside, quartz, calcite, and vesuvianite are also present. Mineral chemistry variations across the deposit are minor, and the absence of inclusions indicates textural and chemical equilibrium. The wollastonite-bearing rocks have unusually low mineral δ18O values: –0.6 to +2.2‰ for garnet, –0.2 to +2. 6‰ for clinopyroxene, and –0.2 to +0.4‰ for wollastonite. Calcite δ18O values range from 6.8 to 11. 8‰ and δ13C values from –6.4 to –3.2‰. Calcite δ18O values are unusually low for calc-silicate rocks, but Δcalcite-garnet values from 3 to 12‰ indicate O-isotope disequilibrium between calcite and the silicate minerals. Garnet-biotite metapelitic and diopside gneisses have unexpectedly low δ18O values (<7‰). The approach to O-isotope equilibrium displayed by coexisting silicate minerals, and low mineral δ18O values in calc-silicate and metapelite and metapsammite gneisses, is consistent with low δ18O values being acquired before peak metamorphism. Low δ18O values in the minerals of the calc-silicate rocks require interaction with external fluid at high water/rock ratio. We suggest that the deposit represents a metamorphosed skarn that developed at the contact between the original carbonate rocks and intruding felsic magmas.


2018 ◽  
Vol 59 (9) ◽  
pp. 1731-1762 ◽  
Author(s):  
S Braunger ◽  
M A W Marks ◽  
B F Walter ◽  
R Neubauer ◽  
R Reich ◽  
...  

Abstract The Miocene Kaiserstuhl Volcanic Complex (Southwest Germany) consists largely of tephritic to phonolitic rocks, accompanied by minor nephelinitic to limburgitic and melilititic to haüynitic lithologies associated with carbonatites. Based on whole-rock geochemistry, petrography, mineralogy and mineral chemistry, combined with mineral equilibrium calculations and fractional crystallization models using the Least Square Fitting Method, we suggest that the Kaiserstuhl was fed by at least two distinct magma sources. The most primitive rock type of the tephritic to phonolitic group is rare monchiquite (basanitic lamprophyre) evolving towards tephrite, phonolitic tephrite, phonolitic noseanite, nosean phonolite and tephritic phonolite by fractional crystallization of variable amounts of clinopyroxene, amphibole, olivine, spinel/magnetite, garnet, titanite, plagioclase and nosean. During this evolution, temperature and silica activity (aSiO2) decrease from about 1100°C and aSiO2 = 0·6–0·8 to 880°C and aSiO2 = ∼0·2. At the same time, oxygen fugacity (fO2) increases from ΔFMQ* = +2–3 to ΔFMQ* = +3–5, with ΔFMQ* being defined as the log fO2 deviation from the silica activity-corrected FMQ buffer curve. Nephelinitic rocks probably derive by fractionation of mostly olivine, spinel/magnetite, melilite, perovskite and nepheline from an olivine melilititic magma. The nephelinitic rocks were formed at similarly high crystallization temperatures (>1000°C) and evolve towards limburgite (hyalo-nepheline basanite) by an increase of silica activity from about aSiO2 = 0·4–0·5 to aSiO2 = 0·5–0·9, whilst redox conditions are buffered to ΔFMQ* values of around +3. Haüyne melilitite and the more evolved (melilite) haüynite may equally be derived from an olivine melilitite by more intense olivine and less melilite fractionation combined with the accumulation of haüyne, clinopyroxene and spinel. These rocks were crystallized at very low silica activities (aSiO2 ≤0·2) and highly oxidized conditions (ΔFMQ* = +4–6). Even higher oxygen fugacities (ΔFMQ* = +6–7) determined for the carbonatite suggests a close genetic relation between these two groups. The assemblage of carbonatites with highly oxidized silicate rocks is typical of many carbonatite occurrences worldwide, at least for those associated with melilititic to nephelinitic silicate rocks. Therefore, we suggest that the existence of highly oxidized carbonate-bearing sublithospheric mantle domains is an important prerequisite to form such complexes.


2014 ◽  
Vol 25 (4) ◽  
pp. 369-377 ◽  
Author(s):  
Shijie Li ◽  
Shijie Wang ◽  
Shen Liu ◽  
Xiongyao Li ◽  
Yang Li ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document