Metamorphism of the Arseno Lake area, N.W.T., Canada: an Abukuma facies series of Aphebian age

1986 ◽  
Vol 23 (5) ◽  
pp. 646-669
Author(s):  
Peter A. Nielsen

Progressive mineralogical and mineral–chemical changes are described for metapelitic rocks from an Abukuma-type metamorphic series ranging from greenschist to upper amphibolite – granulite facies in the Bear Structural Province, Northwest Territories, Canada.The first appearance of the following minerals defines six isograds: biotite; andalusite; cordierite (muscovite + chlorite out); sillimanite (andalusite out); sillimanite + K-feldspar (muscovite + quartz out); and almandine + K-feldspar ± cordierite (biotite + sillimanite + quartz out).Electron microprobe analyses of the Fe–Mg silicates, biotite, cordierite, and garnet, display two distinct trends of mineral chemistry with increasing metamorphic grade. In the almandine + K-feldspar ± cordierite zone, where garnet is present, Fe/(Fe + Mg) decreases in all of the Fe–Mg silicates observed. However, in the cordierite zone and in the higher grade rocks where garnet is absent, Fe/(Fe + Mg) increases in both biotite and cordierite. Ilmenite and rutile are involved in all continuous reactions and lead to increasing Fe/Mg with grade unless garnet is a product of reaction. There is also a displacement towards lower Fe content at the sillimanite + K-feldspar isograd.The scale of equilibration decreases to 1–2 mm in the almandine + K-feldspar ± cordierite zone, which is most probably a function of the decrease of [Formula: see text] and therefore [Formula: see text]in the metamorphic fluid with increasing metamorphic grade.The physical conditions of metamorphism in the Arseno Lake area range from [Formula: see text] at 2–2.5 kbar with[Formula: see text] in the chlorite zone to ≥650 °C at 3.5–4.0 kbar where [Formula: see text] in the almandine + K-feldspar ± cordierite zone.

1982 ◽  
Vol 19 (9) ◽  
pp. 1759-1774 ◽  
Author(s):  
Dexter Perkins III ◽  
Eric J. Essene ◽  
Louise Annette Marcotty

Grenville rocks from a 2500 km2 area centered on Otter Lake, Quebec (some 75 km northwest of Ottawa) are in the uppermost amphibolite to lower granulite facies; orthopyroxene occurs occasionally in both metabasic and charnockitic rocks. The temperature of metapmorphism was approximately 675 °C, based upon oxide, feldspar, and garnet–clinopyroxene thermometry. Little thermal gradient could be detected across the area. Carbonate thermometry, using reintegrated calcite compositions, yielded lower temperatures of 600 °C (maximum), while garnet–biotite and other Kd thermometers yielded scattered and for the most part unreasonable results. Metamorphic pressure, calculated from the reaction anorthite = grossular + sillimanite + quartz, was 5.0 ± 0.5 kbar(500 ± 50 MPa). Similar calculations based upon the reactions garnet + quartz = anorthite + orthopyroxene and garnet + quartz = anorthite + clinopyroxene yielded pressures of 5.5–7.0 kbar (550–700 MPa). Pressure calculations based upon assemblages of cordierite–garnet–sillimanite–quartz were less precise, but agreed with the outer estimates. Similar metamorphic temperatures and slightly lower pressures have been estimated for the Adirondack Lowlands of New York. In the Morin Highlands, 100 km east of Otter Lake, and in the Adirondack Highlands, 100 km east of the Adirondack Lowlands, temperatures of metamorphism (700–800 °C) and pressures of metamorphism (6–9 kbar (600–900 MPa)) are both higher. Thus it appears that over an approximate 300 km north–south direction nearly constant metamorphic conditions prevailed at Grenville time. In the east–west direction significant variations in metamorphic grade are recorded; both temperature and pressure markedly increase to the east.


1977 ◽  
Vol 14 (8) ◽  
pp. 1740-1752
Author(s):  
Hewitt H. Bostock

The compositions of seven pairs of coexisting hornblende and grunerite and five assemblages of coexisting hornblende, grunerite, and garnet from Archean silicate iron formation of low and medium metamorphic grade have been obtained by electron microprobe analysis. Important factors affecting the composition of the amphiboles are: (1) the Mg/Fe ratio of the iron-formation beds, which controls the gross Mg/Fe ratio of the amphiboles; (2) the alumina content of the beds, which affects the degree of alumina substitution in hornblende thereby altering the distribution of Mg and Fe in the coexisting amphiboles; and (3) the occurrence of iron-rich garnet, which produces higher Mg/Fe ratios in both amphiboles. A fourth potentially important factor, the oxygen fugacity, cannot be satisfactorily assessed with these data, but has not obscured the effects of the other three. Temperature of crystallization of the amphiboles was an important factor mainly insofar as it affected the crystallization of garnet in the alumina-rich rocks.Four coexisting hornblende–cummingtonite pairs from metatuffs show similar control of Mg–Fe fractionation by alumina substitution in hornblende.


Minerals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 446
Author(s):  
Zhiming Xu ◽  
Chengquan Wu ◽  
Zhengwei Zhang ◽  
Jinhong Xu ◽  
Xiyao Li ◽  
...  

Manganese and Fe have similar geochemical properties in the supergene environment. Separation of Mn and Fe is an important process for the formation of high-grade sedimentary manganese deposits. Large-scale manganese carbonate deposits (total reserves of approximately 700 Mt) were formed during the interglacial of the Sturtian and Marinoan in South China. The orebodies are hosted in the black rock series at the basal Datangpo Formation of the Cryogenian period. The Fe contents in ores range from 1.15 to 7.18 wt.%, with an average of 2.80 wt.%, and the average Mn/Fe ratio is 8.9, indicating a complete separation of Mn and Fe during the formation of manganese ores. Here, we present element data of manganese carbonates and sulfur isotopes of pyrite from the Dawu deposit, Guizhou, China, aiming to investigate the separation mechanism of Mn and Fe and the ore genesis. The Fe in ores mainly occurs as carbonate (FeCO3) and pyrite (FeS2). The Mn, Ca, Mg and Fe exist in the form of isomorphic substitutions in manganese carbonate. The contents of FeCO3 in manganese carbonates are similar in different deposits, with averages of 2.6–2.8 wt.%. The whole-rock Fe and S contents have an obvious positive correlation (R = 0.69), indicating that the difference of whole-rock Fe content mainly comes from the pyrite content. The δ34SV-CDT of pyrite varies from 40.0 to 48.3‰, indicating that the pyrite formed in a restricted basin where sulfate supply was insufficient and the sulfate concentrations were extremely low. Additionally, the whole-rock Fe content is negatively correlated with the δ34S values of the whole-rock and pyrite, with correlation coefficients of −0.78 and −0.83, respectively. Two stages of separations of Mn and Fe might have occurred during the mineralization processes. The reduced seawater became oxidized gradually after the Sturtian glaciation, and Fe2+ was oxidized and precipitated before Mn2+, which resulted in the first-stage separation of Mn and Fe. The residual Mn-rich and Fe-poor seawater flowed into the restricted rift basin. Mn and Fe were then precipitated in sediments as oxyhydroxide as the seawater was oxidized. At the early stage of diagenesis, organic matter was oxidized, and manganese oxyhydroxide was reduced, forming the manganese carbonate. H2S was insufficient in the restricted basin due to the extremely low sulfate concentration. The Fe2+ was re-released due to the lack of H2S, resulting in the second-stage separation of Mn and Fe. Finally, the manganese carbonate deposit with low Fe and very high δ34S was formed in the restricted basin after the Sturtian glaciation.


2005 ◽  
Vol 142 (3) ◽  
pp. 255-268 ◽  
Author(s):  
M. SANTOSH ◽  
A. S. COLLINS ◽  
T. MORIMOTO ◽  
K. YOKOYAMA

We report U–Pb electron microprobe (zircon and monazite) and Secondary Ion Mass Spectrometry (SIMS) U–Pb (zircon) ages from a granulite-facies metapelite and a garnet–biotite gniess from Chittikara, a classic locality within the Trivandrum Block of southern India. The majority of the electron-microprobe data on zircons from the metapelite define apparent ages between 1500 and 2500 Ma with a prominent peak at 2109±22 Ma, although some of the cores are as old as 3070 Ma. Zircon grains with multiple age zoning are also detected with 2500–3700 Ma cores, 1380–1520 mantles and 530–600 Ma outer rims. Some homogeneous and rounded zircon cores yielded late Neoproterozoic ages that suggest that deposition within the Trivandrum Block belt was younger than 610 Ma. The outermost rims of these grains are characterized by early Cambrian ages suggesting metamorphic overgrowth at this time. The apparent ages of monazite grains from this locality reveal multiple provenance and polyphase metamorphic history, similar to those of the zircons. In a typical case, Palaeoproterozoic cores (1759–1967 Ma) are enveloped by late Neoproterozoic rims (562–563 Ma), which in turn are mantled by an outermost thin Cambrian rim (∼515 Ma). PbO v. ThO*2 plots for monazites define broad isochrons, with cores indicating a rather imprecise age of 1913±260 Ma (MSWD=0.80) and late Neoproterozoic/Cambrian cores as well as thin rims yielding a well-defined isochron with an age of 557±19 Ma (MSWD=0.82). SIMS U–Pb isotopic data on zircons from the garnet–biotite gneiss yield a combined core/rim imprecise discordia line between 2106±37 Ma and 524±150 Ma. The data indicate Palaeoproterozoic zircon formation with later partial or non-uniform Pb loss during the late Neoproterozoic/Cambrian tectonothermal event. The combined electron probe and SIMS data from the metapelite and garnet–biotite gneiss at Chittikara indicate that the older zircons preserved in the finer-grained metapelite protolith have heterogeneous detrital sources, whereas the more arenaceous protolith of the garnet–biotite gniess was sourced from a single-aged terrane. Our data suggest that the metasedimentary belts in southern India may have formed part of an extensive late Neoproterozoic sedimentary basin during the final amalgamation of the Gondwana supercontinent.


1976 ◽  
Vol 13 (9) ◽  
pp. 1201-1211 ◽  
Author(s):  
N. B. W. Harris ◽  
A. M. Goodwin

The eastern Lac Seul region of the English River Gneiss Belt is divided into two domains defined by contrasting petrology and structure. The northern domain is underlain by east-trending, steeply south-dipping, migmatized metasediments, intruded by occasional granite sills, and the southern domain by gneissic tonalite and trondhjemite, with abundant amphibolite inclusions, intruded by granite dykes and diapirs: this domain has a complex structure with gently east-plunging open folds of about 5 km wavelength. Field evidence suggests that metasediments of the northern domain have been deposited on the tonalite trondhjemite basement, which was subsequently mobilized, thereby producing the steeply dipping paragneiss belt of the northern domain.The grade of metamorphism throughout the region lies in the upper amphibolite facies, rising locally to the granulite facies. Within 15 km of the southern margin of the gneiss belt, the metamorphic grade decreases to the greenschist facies.U–Pb dating of zircons indicates that the tonalite gneiss was emplaced at least 3040 m.y. ago, and the granite plutons at 2660 m.y., coeval with migmatization and upper amphibolite facies metamorphism. Late pegmatites were emplaced at 2560 m.y.


Clay Minerals ◽  
1997 ◽  
Vol 32 (2) ◽  
pp. 205-222 ◽  
Author(s):  
P. Árkai ◽  
D. Sadek Ghabrial

AbstractX-ray diffraction chlorite crystallinity (ChC) indices and major element chemical compositions of chlorites and bulk rocks were determined and correlated in meta-igneous rocks from different Mesozoic formations in various tectonic units of the Bükk Mountains, NE Hungary. The rocks, of basic to acidic compositions, range from ocean-floor metamorphic prehnite-pumpellyite facies (diagenetic zone) through regional metamorphic prehnite-pumpellyite facies (anchizone) up to the regional metamorphic pumpellyite-actinolite and greenschist facies (epizone). As in the case of meta-sedimentary rocks, chlorite crystallinity can be applied as an empirical, complementary petrogenetic tool to determine relative differences in grades of low-temperature meta-igneous rocks. Electron microprobe and XRD data show that ChC is controlled mainly by the decreasing amounts of contaminants (mixed-layered components or discrete, intergrown phases of mostly smectitic composition) in chlorite with advancing metamorphic grade, up to the epizone. The apparent increase in calculated Aliv content of chlorite with increasing temperature is related to the decrease of these contaminants, as stated earlier by Jiang et al. (1994). On the basis of the significant correlations found between ChC and temperatures, derived by the chlorite-Aliv geothermometer of Cathelineau (1988), both methods may be used for estimating the approximate temperatures of metamorphism, in spite of the contrasting interpretation of chemical data from chlorites obtained by electron microprobe analyses. After determining the effects of changing bulk chemistry on chlorite composition and ChC, the chlorite crystallinity method may complement the correlation of the illite crystallinity-based zonal classification of meta-sediments and the mineral facies classification of meta-igneous rocks.


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