Zircon ages and the distribution of Archaean and Proterozoic rocks in the Rauer Islands

1993 ◽  
Vol 5 (2) ◽  
pp. 193-206 ◽  
Author(s):  
P. D. Kinny ◽  
L. P. Black ◽  
J. W. Sheraton

The application of zircon U-Pb geochronology using the SHRIMP ion microprobe to the Precambrian high-grade metamorphic rocks of the Rauer Islands on the Prydz Bay coast of East Antarctica, has resulted in major revisions to the interpreted geological history. Large tracts of granitic orthogneisses, previously considered to be mostly Proterozoic in age, are shown here to be Archaean, with crystallization ages of 3270 Ma and 2800 Ma. These rocks and associated granulite-facies mafic rocks and paragneisses account for up to 50% of exposures in the Rauer Islands. Unlike the 2500 Ma rocks in the nearby Vestfold Hills which were cratonized soon after formation, the Rauer Islands rocks were reworked at about 1000 Ma under granulite to amphibolite facies conditions, and mixed with newly generated felsic crust. Dating of components of this felsic intrusive suite indicates that this Proterozoic reworking was accomplished in about 30–40 million years. Low-grade retrogression at 500 Ma was accompanied by brittle shearing, pegmatite injection, partial resetting of U-Pb geochronometers and growth of new zircons. Minor underformed lamprophyre dykes intruded Hop and nearby islands later in the Phanerozoic. Thus, the geology of the Rauer Islands reflects reworking and juxtaposition of unrelated rocks in a Proterozoic orogenic belt, and illustrates the important influence of relatively low-grade fluid-rock interaction on zircon U-Pb systematics in high-grade terranes.

2010 ◽  
Vol 47 (6) ◽  
pp. 927-940 ◽  
Author(s):  
J. V. Owen ◽  
R. Corney ◽  
J. Dostal ◽  
A. Vaughan

The Liscomb Complex comprises Late Devonian intrusive rocks (principally peraluminous granite) and medium- to high-grade metamorphic rocks (“gneisses”) that collectively are hosted by low-grade (greenschist facies) metasediments of the Cambro-Ordovician Meguma Group. The conventional view that these “gneisses” contain high-grade mineral assemblages and represent basement rocks has recently been challenged, and indeed, some of the rocks previously mapped as gneisses, particularly metapelites, have isotopic compositions resembling the Meguma Group. Amphibole-bearing enclaves in the Liscomb plutons, however, are isotopically distinct and in this regard resemble xenoliths of basement gneisses in the Popes Harbour lamprophyre dyke, south of the Liscomb area. Metasedimentary enclaves with Meguma isotopic signatures can contain garnets with unzoned cores (implying high temperatures) that host high-grade minerals (prismatic sillimanite, spinel, and (or) corundum) and are enclosed by retrograde-zoned rims. These features are interpreted here as having formed during and following the attainment of peak temperatures related to Liscomb magmatism. The amphibole-bearing meta-igneous rocks described here contain cummingtonite or hornblendic amphibole and occur as enclaves in granodioritic to tonalitic plutons. They are mineralogically, texturally, and isotopically distinct from Meguma metasediments and at least some of the plutonic rocks that enclose them, so remain the most likely candidate for basement rocks in the Liscomb Complex.


1994 ◽  
Vol 31 (7) ◽  
pp. 1096-1103 ◽  
Author(s):  
T. E. Krogh ◽  
D. E. Moser

A decade of U–Pb dating of zircon and monazite from high-grade metamorphic rocks in the Kapuskasing uplift has identified a series of magmatic and metamorphic events between 2700 and 2585 Ma, and indicates that the onset of regional granulite metamorphism took place at mid-crustal levels of the southern Superior craton ca. 2660 Ma. New U–Pb ages for zircon and monazite have been used to constrain the age of ductile deformation fabrics at two sites in the Ivanhoe Lake fault zone, the structure along which the granulite-facies Kapuskasing structural zone was uplifted. These results suggest that the fault zone was probably active in the late Archean (as young as 2630 Ma) and again at approximately 2500 Ma.


2020 ◽  
Vol 61 (6) ◽  
Author(s):  
Ronald J Bakker ◽  
Evgenii Pushkarev ◽  
Anna P Biryuzova

Abstract High-grade metamorphic rocks underlying the intrusive layered dunite–pyroxenite–gabbronorite East-Khabarny Complex (EKC) are integrated in the complex Khabarny mafic–ultramafic Massif in the Sakmara Allochthon zone in the Southern Urals. These rocks are associated with high-temperature shear zones. Garnetites from the upper part of the metamorphic unit close to the contact with EKC gabbronorite are chemically and texturally analysed to estimate their formation conditions and fluid regime. Fluids provide crucial information of formation conditions and evolution of these garnetites during high-grade metamorphism, and are preserved in channel positions within Si6O1812- rings of cordierite, and in fluid inclusions in quartz and garnet. Minerals and fluid inclusions of the garnetites are studied with X-ray fluorescence spectrometry, electron microprobe analyses, Raman spectroscopy, and microthermometry. The garnetites mainly consist of garnet (up to 80 vol. %), cordierite and quartz. Accessory minerals are rutile, ilmenite, graphite, magnetite and cristobalite. Granulite-facies metamorphic conditions of the garnetites are estimated with the garnet–cordierite–sillimanite–quartz geothermobarometer: temperatures of 740 to 830 ˚C and pressures of 770–845 MPa. The average garnet composition in end-member concentrations is 48·5 mole % almandine (±3·9), 34·7 mole % pyrope (±3·3), 10·3 mole % spessartine (±1·1), 1·8 mole % grossular (±1·5), and 1·5 mole % andradite (±1·5). The cordierite electron microprobe analyses reveal an average Mg2+ fraction of 0·79 ± 0·01 in the octahedral site. Relicts of a strong positive temperature anomaly (up to 1000 ˚C) are evidenced by the preservation of cristobalite crystals in garnet and the high titanium content of quartz (0·031 ± 0·008 mass % TiO2) and garnet (0·31 ± 0·16 mole % end-member Schorlomite-Al). The fluid components H2O, CO2, N2 and H2S are detected in cordierite, which correspond to a relatively oxidized fluid environment that is common in granulites. In contrast, a highly reduced fluid environment is preserved in fluid inclusions in quartz nodules, which are mono-fluid phase at room temperature and composed of CH4 (>96 mole %) with locally minor amounts of C2H6, N2, H2S and graphite. The fluid inclusions occur in homogeneous assemblages with a density of 0·349 to 0·367 g·cm-3. The CH4-rich fluid may represent peak-temperature metamorphic conditions, and is consistent with temperature estimation (∼1000 ˚C) from Ti-in-garnet and Ti-in-quartz geothermometry. Tiny CH4-rich fluid inclusions (diameter 0·5 to 2 µm) are also detected by careful optical analyses in garnet and at the surface of quartz crystals that are included in garnet grains. Graphite in fluid inclusions precipitated at retrograde metamorphic conditions around 300–310 ± 27 ˚C. Aragonite was trapped simultaneously with CH4-rich fluids and is assumed to have crystallized at metastable conditions. The initial granulite facies conditions that led to the formation of a cordierite and garnet mineral assemblage must have occurred in a relative oxidized environment (QFM-buffered) with H2O–CO2-rich fluids. Abundant intrusions or tectonic emplacement of mafic to ultramafic melts from the upper mantle that were internally buffered at a WI-buffered (wüstite–iron) level must have released abundant hot CH4-rich fluids that flooded and subsequently dominated the system. The origin of the granulite-facies conditions is similar to peak-metamorphic conditions in the Salda complex (Central Urals) and the Ivrea–Verbano zone (Italian Alps) as a result of magmatic underplating that provided an appearance of a positive thermal anomaly, and further joint emplacement (magmatic and metamorphic rocks together) into upper crustal level as a high temperature plastic body (diapir).


1995 ◽  
Vol 118 (4) ◽  
pp. 365-378 ◽  
Author(s):  
J. M. Eiler ◽  
J. W. Valley ◽  
C. M. Graham ◽  
L. P. Baumgartner

2020 ◽  
Author(s):  
Shuyun Cao ◽  
Franz Neubauer ◽  
Meixia Lv

<p>Graphitic carbon exhibits a large range of structures and chemical compositions, from amorphous-like compounds to crystalline graphite. The graphitic carbon-bearing rocks are widely occurred in low- to high- grade metamorphic massif and fault zone. The carbonaceous material in the rock will gradually transform from an amorphous into an ordered crystalline structure by thermal metamorphism, which is called graphitization. The degree of graphitization is believed to be a reliable indicator of peak temperature conditions in the metamorphic rock. In many low-grade metamorphic rocks, graphitic carbon (e.g., soot, low-grade coal) is often associated with brittle fault gouge whereas in high-grade metamorphic rocks, graphitic carbon (crystalline granite) are most commonly seen in marble, schist or gneiss. In recent years, graphitic carbon-bearing rocks have been reported from natural fault zones (reviwers paper see Cao and Neubauer 2019 and references therein). The graphitic carbon grains in our samples tend to enrich in slip-surface or micro-shear zone with strain localization in fault, performed as dislocation glide of deformation. The graphite LPO shows slip system in the direction of basil <a> combined basil <a> slip and weak prism <a> slip systems, suggesting a low-temperature to a medium to high temperature deformation conditions, which is in consistent with the results of Raman Spectra of Carbonaceous material (RSCM) thermometry. We also proposed that the graphitic carbon formed in the rocks can significantly affect the mechanical properties of the fault during the process of faulting. This process can effectively cause reaction weakening and strain localization, which is thought to play an important role as solid lubrication in fault weakening.</p>


1985 ◽  
Vol 123 ◽  
pp. 1-39
Author(s):  
R.F Cheeney

Layered metamorphic formations in southern Liverpool Land are disposed in dome-shaped structures with inclinations everywhere gentie. Meta-igneous and meta-sedimentary rock types are represented as well as formations of less clear affinities. Rocks of eclogitic character comprise part of one of the formations which, together with others of the layered succession, passes laterally into a less-deformed complex containing discordant contact relations of plutonic igneous type. The Hurry Inlet granite is a posttectonic, post-metamorphic formation cropping out in the extreme north-west of the area. The earliest detectable events indicate emplacement of granodiorite into sedimentary or metasedimentary formations. Subsequently, these rocks of igneous and sedimentary origin were raised to upper amphibolite or granulite facies with some deformation leading to the prominent layering and including, perhaps, their juxtaposition with eclogitic rocks originating at great depth. Retrogression to 'normal' amphibolite facies followed, with widespread development of hydrous minerals, pegmatites, etc. The position of limited cataclasis with respect to this later stage of metamorphism is not abundantly clear. Emplacement of the Hurry Inlet granite entirely post-dates all of these events.


Author(s):  
S. W. Morel

SummaryThe mineral assemblages developed in a variety of high-grade metamorphic rocks from southern Nyasaland are compared with standard metamorphic facies mineral assemblages proposed by some authors.


Clay Minerals ◽  
2008 ◽  
Vol 43 (4) ◽  
pp. 561-574
Author(s):  
E. T. Sokalska ◽  
E. Dubińska ◽  
G. Kaproń ◽  
J. A. Kozubowski ◽  
M. Walski

AbstractThe mafic rocks from boreholes studied here contain the assemblage typical for upper-subgreenschist to lower-greenschist facies (albite, chlorite, illite, titanite, quartz, Ti-oxide ± actinolite) as well as relict clinopyroxene.Metapelites underlying a metabasic rock sequence also record metamorphic alteration as demonstrated by the chlorite and illite crystallinities. Chlorite crystallinity suggests formation in conditions close to the subgreenschist/greenschist facies boundary, but this mineral is partly decomposed during metamorphic retrogression.


2021 ◽  
Author(s):  
Aaron Bufe ◽  
Kristen L. Cook ◽  
Albert Galy ◽  
Hella Wittmann ◽  
Niels Hovius

Abstract. The denudation of rocks in mountain belts exposes a range of fresh minerals to the surface of the Earth that are chemically weathered by acidic and oxygenated fluids. The impact of the resulting coupling between denudation and weathering rates fundamentally depends on the types of minerals that are weathering. Whereas silicate weathering sequesters CO2, the combination of sulfide oxidation and carbonate dissolution emits CO2 to the atmosphere. Here, we combine the concentrations of dissolved major elements in stream waters with 10Be basin-wide denudation rates from 35 small catchments in eastern Tibet to elucidate the importance of lithology in modulating the relationships between denudation rate, chemical weathering pathways, and CO2 consumption or release. Our catchments span three orders of magnitude in denudation rate in low-grade flysch, high grade metapelites, and granitoid rocks. For each stream, we estimate the concentrations of solutes sourced from silicate weathering, carbonate dissolution, and sulfide oxidation using a mixing model. We find that for all lithologies, cation concentrations from silicate weathering are largely independent of denudation rate, but solute concentrations from carbonates and, where present, sulfides increase with increasing denudation rate. With increasing denudation rates, weathering may, therefore, shift from consuming to releasing CO2 in both (meta)sedimentary and granitoid lithologies. We find that catchments draining high grade metamorphic rocks have systematically higher concentrations of sulfate from sulfide weathering than catchments containing weakly metamorphosed sediments. Moreover, our data provide tentative evidence that sulfate concentrations in these catchments are potentially more sensitive to denudation rate. We propose that changes in the sulfur oxidation state during prograde metamorphism of pelites in the mid-crust could lead to sulfate reduction that is even more complete than in low-grade sediments and provides a larger sulfide source for oxidation upon re-exposure of the rocks. In this case, the elevated concentration of sulfate in catchments draining high-grade metapelites would suggest that exposure of an increasing fraction of metamorphic rocks during orogenesis could lead to a boost in the release of CO2 that is independent of denudation rate.


Author(s):  
Gejing Li ◽  
D. R. Peacor ◽  
D. S. Coombs ◽  
Y. Kawachi

Recent advances in transmission electron microscopy (TEM) and analytical electron microscopy (AEM) have led to many new insights into the structural and chemical characteristics of very finegrained, optically homogeneous mineral aggregates in sedimentary and very low-grade metamorphic rocks. Chemical compositions obtained by electron microprobe analysis (EMPA) on such materials have been shown by TEM/AEM to result from beam overlap on contaminant phases on a scale below resolution of EMPA, which in turn can lead to errors in interpretation and determination of formation conditions. Here we present an in-depth analysis of the relation between AEM and EMPA data, which leads also to the definition of new mineral phases, and demonstrate the resolution power of AEM relative to EMPA in investigations of very fine-grained mineral aggregates in sedimentary and very low-grade metamorphic rocks.Celadonite, having end-member composition KMgFe3+Si4O10(OH)2, and with minor substitution of Fe2+ for Mg and Al for Fe3+ on octahedral sites, is a fine-grained mica widespread in volcanic rocks and volcaniclastic sediments which have undergone low-temperature alteration in the oceanic crust and in burial metamorphic sequences.


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