scholarly journals Paleoproterozoic Metamorphism of the Archean Tuntsa Suite, Northern Fennoscandian Shield

Minerals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1034
Author(s):  
Pentti Hölttä ◽  
Tiia Kivisaari ◽  
Hannu Huhma ◽  
Gavyn Rollinson ◽  
Matti Kurhila ◽  
...  

The Tuntsa Suite is a polymetamorphic Archean complex mainly consisting of metasedimentary gneisses. At least two strong metamorphic events can be distinguished in the area. The first took place at high temperatures in the Neoarchean at around 2.70–2.64 Ga, indicated by migmatisation and U-Pb ages of metamorphic zircon. During the Paleoproterozoic, metasedimentary gneisses were penetratively deformed and recrystallized under medium pressures producing staurolite, kyanite and garnet-bearing mineral assemblages. The suggested Paleoproterozoic PT path was clockwise where the temperature and pressure first increased to 540–550 °C and 6 kbar, crystallizing high Ca/low Mg garnet cores. The mineral compositions show that commonly garnet core was not in chemical equilibrium with staurolite but crystallized earlier, although garnet-staurolite-kyanite assemblages are common. The temperature and pressure increased to c. 650 °C and 8 kbars where staurolite and kyanite coexist. This was followed by decompression down to c. 550–600 °C and 3–4 kbars, shown by andalusite crystallization and cordierite formed in the breakdown of staurolite and biotite + kyanite. The observed garnet zoning where Mg increases and Ca decreases from the core to the rim was developed with both increasing and decreasing pressure, depending on the effective bulk composition. The U-Pb and Sm-Nd age determinations for monazite and garnet show that the Paleoproterozoic metamorphic cycle took place at 1.84–1.79 Ga, related with thrusting of the Lapland granulites onto the adjacent terranes and subsequent exhumation.

1971 ◽  
Vol 8 (9) ◽  
pp. 1065-1080 ◽  
Author(s):  
C. J. N. Fletcher

Six mineral assemblages have been defined within a small portion of a layered two-pyroxene amphibolite. The relationships between bulk composition, mineral composition, and mineral assemblage were determined from X-ray fluorescence, electron microprobe, and optical data. It is shown that the layer assemblages and the mineral compositions are, in general, directly related to the bulk compositions of the layers. Graphical representation of the phase assemblages is impossible, due to the number of determining components; however, an attempt is made to tabulate the phase relation-ships in 9-space. Linear regression analysis has been used to show that the six mineral assemblages owe their differences purely to different bulk compositions, and that no isochemical reactions can be written between them. The computed equations relating the mineral assemblages indicate that water was immobile during metamorphism.


Correctly formulated thermodynamics provides the only reliable means of applying the results of mineral equilibria experiments to the calculation of the temperature and pressure of formation of mineral assemblages. The problems of formulating geothermometers and geobarometers are considered with particular reference to calculating the conditions of formation of garnet lherzolites in kimberlites. Incorrect expressions for the thermodynamics of minerals will provide unreliable methods for calculating conditions of formation. The reactions on which these methods are based must be chosen so that composition parameters which are uncertain in a mineral analysis (for example, the amounts of ferrous iron on each octahedral site in a pyroxene) do not have a central position in a method. For this reason it is suggested that the use of alumina solubility in enstatite in equilibrium with garnet is not suitable as a geobarometer for garnet lherzolites. The orthopyroxene-Ca-rich clinopyroxene miscibility gap geothermometer is shown to be very sensitive to the mineral compositions when more correctly formulated, treating the pyroxenes as non-ideal solutions. Two new methods are presented which are based on Ca-Mg exchange reactions involving orthopyroxene-Ca-rich clinopyroxene and orthopyroxene-garnet. These methods allow the calculation of both temperature and pressure for garnet lherzolites. It is observed that the sheared lherzolites and the granular lherzolites formed at lower pressures than has been suggested previously, implying a steeper geotherm at the time the minerals attained their present compositions.


Geosciences ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 439
Author(s):  
Norbert Clauer ◽  
Edward Keppens ◽  
I. Tonguç Uysal ◽  
Amélie Aubert

A combined ultrasonic treatment, with de-ionized H2O, dilute HAc or dilute HCl, of three Mid-Miocene glauconite samples was applied to K–Ar date the different separates in order to compare the results with those obtained by the Rb–Sr method using the same three samples and that were analyzed strictly in the same way. Two aliquots yield opposite elemental and K–Ar trends, which suggests different initial mineral compositions for the various pellets. The K–Ar data of two untreated and leached L7 and L8 aliquots are almost within analytical uncertainty from 17.3 ± 0.6 Ma to 19.6 ± 0.7 Ma (2σ), while those of the third L10 sample are slightly higher at 22.1 ± 1.2 Ma (2σ). Comparatively, the earlier published Rb–Sr ages of the three untreated samples and of the leached aliquots gave similar data for the L7 aliquots by an isochron at 18.1 ± 3.1 (2σ) Ma and for the sample L8 by an isochron with an age of 19.6 ± 1.8 (2σ) Ma, while the untreated L10 aliquot yields a very high Rb–Sr date of 42.1 ± 1.6 (2σ) Ma. This untreated L10 glauconite fraction contains blödite, a Sr-rich carbonate that impacted the two isotopic systems differently. Generally, dilute HCl or HAc acids dissolve carbonates, sulfates, sulfites and oxides, while they do not affect the clay-type crystals such as glauconites. These soluble minerals can be identified indirectly, as here, by X-ray diffraction and the amounts of leached Na2O, CaO and Fe2O3 contents. Together with the leaching of some metallic trace elements, those of NaO confirm the leaching of metals and of blödite that are both hosted by the glauconite pellets. The occurrence of this Sr-enriched mineral explains the age differences of the non-treated aliquots and suggests a systematic leaching of any glauconite separate before isotope determination and, possibly, a comparison of the Rb–Sr and K–Ar results. Ultrasonic shaking appears appropriate for physical disaggregation of any contaminating grains that may remain hosted within the pellets, even after a preliminary H2O wash, which may dissolve and remove the soluble minerals but not the H2O-insoluble silicates. The K–Ar study completed here as a complement to a previous Rb–Sr study highlights, again, the importance of the preparation step in isotopic studies of glauconite-type and, by extension, of any clay material, as all occurring minerals can interfere in the final age determinations and, therefore, differently in the mineral assemblages. All those not in isotopic equilibrium need to be removed before analysis, including the soluble Sr or alkali-enriched ones.


1987 ◽  
Vol 51 (361) ◽  
pp. 409-415 ◽  
Author(s):  
R. G. Warren ◽  
B. J. Hensen

AbstractSpecimens collected from a small lens of phlogopite-rich rock in the granulite-facies terrain of the Arunta Block, central Australia, have unusual bulk compositions and mineral assemblages. One sample consists of phlogopite enclosing blue spinel (mg 96) with minute granules of corundum and sapphirine at the margins; a second of phlogopite enclosing porphyroblasts of corundum and peraluminous sapphirine. In the first the sapphirine is close to the 7 : 9 : 3 composition; in the other it is markedly peraluminous, e.g. (Mg1.628Fe0.028)Al4.714Si0.636O10, intermediate between the 7 : 9 : 3 and 3 : 5 : 1 members. The texture suggests that this sapphirine is a stable phase in equilibrium with eastonitic phlogopite and corundum. The very potassic, very magnesian bulk composition of the rocks is attributed to potassium metasomatism of a protolith consisting of magnesian chlorite and quartz.


1998 ◽  
Vol 62 (2) ◽  
pp. 213-224 ◽  
Author(s):  
J. R. Ashworth ◽  
V. V. Reverdatto ◽  
V. YU. kolobov ◽  
V. V. Lepetyukha ◽  
V. S. Sheplev ◽  
...  

AbstrsctIn a granulite from the Kokchetav massif, a complex mineral assemblage and intricate textures have resulted from a combination of unusual rock composition and two–stage metamorphic history. The second, contact metamorphism produced mainly cordierite and anthophyllite, reflecting a bulk composition attributed to pre–metamorphic alteration of basic igneous rock. From the first, highpressure metamorphism, garnet relics persist while another mineral has been completely pseudomorphed. The garnet is partly replaced by a symplectite of three minerals: orthopyroxene vermicules in a coarser intergrowth of cordierite and calcic plagioclase. Despite variable proportions of cordierite and plagioclase, the Al:Si ratio of the symplectite is almost constant, because the proportion of orthopyroxene is smaller where the dominant aluminous mineral is cordierite (Al:Si ≈ 0.8) than where the even more aluminous plagioclase (Al:Si ≈ 0.89) is prominent. The bulk Al:Si ratio of this symplectite, approximately 0.69, is very close to that of reactant garnet (0.66), indicating that Al and Si have been retained almost completely during the local reaction, while other elements were more mobile. In the pseudomorphs, aluminous cores (with Al:Si ratios 1.61–1.93) indicate that the mineral which has been completely replaced was probably kyanite. These cores comprise plagioclase, zoisite, corundum and spinel, and are surrounded by layers of plagioclase and cordierite. Fe, Mg, and Ca have diffused to the core, through layers with low bulk concentrations of these elements, probably by grainboundary diffusion in the solid state.


Mineralogia ◽  
2008 ◽  
Vol 39 (1-2) ◽  
pp. 7-30 ◽  
Author(s):  
Elizabeth Catlos ◽  
Courteney Baker ◽  
Ibrahim Çemen ◽  
Cenk Ozerdem

Whole rock major element influences on monazite growth: examples from igneous and metamorphic rocks in the Menderes Massif, western TurkeyMonazite (LREEPO4) is a radiogenic, rare-earth bearing mineral commonly used for geochronology. Here we examine the control of major element chemistry in influencing the crystallization of monazite in granites (Salihli and Turgutlu bodies) and garnet-bearing metamorphic assemblages (Bozdag and Bayindir nappes) from the Menderes Massif, western Turkey. In S-type granites from the massif, the presence of monazite correlates to the CaO and Al2O3content of the whole rock. Granites with monazite only are low Ca (0.6-1.8 wt% CaO). As CaO increases (from 2.1-4.6 wt%), allanite [(Ce, Ca, Y)2(Al, Fe3+)3(SiO4)3(OH)] is present. Higher Al2O3(>15 wt%) rocks contain allanite and/or monazite, whereas those with lower Al2O3contain monazite only. However, examining data reported elsewhere for A-type granites, the correlation between major element chemistry and presence of monazite is likely restricted to S-type lithologies. Pelitic schists of the Menderes Massif show no correlation between major element chemistry and presence of monazite. One Bayindir nappe sample contains both prograde garnets and those affected significantly by diffusion. These rocks have likely experienced a complicated multi-stage tectonic history, which influenced their current mineral assemblages. The presence of monazite in a metamorphic rock can be influenced by the number, duration, and nature of events that were experienced and the degree to which fluids were involved. The source of monazite in the Bayindir and Bozdag samples was likely reactions that involved allanite. These reactions may not have significantly changed the bulk composition of the rock.


2021 ◽  
Author(s):  
◽  
Jill Fernandes

<p>Scattered, scarce occurrences of garnet- and quartz-rich metamorphic rock, probably derived from Mn- and Fe-rich chert, occur within metamorphosed greywacke sequences worldwide. The metamorphism of such garnetiferous metacherts has not previously been investigated using modern thermodynamic forward modelling techniques due to the lack of appropriate, internally-consistent activity-composition (a–x) models for Mn-bearing minerals. The present study applies thermodynamic forward modelling using the recently-proposed a–x models of White et al. (2014) to investigate the metamorphism of garnetiferous metachert samples from the Southern Alps, New Zealand.  Pressure-temperature (P–T) pseudosections are used in combination with results from petrography, element composition mapping using micro X-ray fluorescence (µXRF) and scanning electron microscope (SEM) methods, and garnet composition data from analytical transects by electron probe microanalysis (EPMA), to study metachert metamorphism. All the samples are compositionally layered, so the possibility exists that an input bulk rock composition might not match the effective bulk composition at the site of garnet growth. If a mineral assemblage stability field in a calculated P–T pseudosection matched the mineral assemblage in the rock, this was taken as an initial indication of a permissible input bulk rock composition. In that case, refined constraints on the P–T conditions were sought by comparing calculated and measured garnet compositions. The studied rocks include samples that are carbonate-bearing, which require consideration of the effects of fluid composition in mixed H₂O–CO₂ fluids, as well as a sample in which the garnet is strongly zoned, texturally-complex, and inferred to be of polymetamorphic origin. The effects of element fractionation by that garnet were investigated by recalculating the P–T pseudosection using a new bulk rock composition with the garnet core content removed. In none of the samples did the calculated and observed composition isopleths for the garnet cores match, suggesting that initial garnet nucleation in these Mn-rich rocks was locally controlled. For most samples in which the calculated and observed mineral assemblages matched, successful estimates of the peak metamorphic conditions were obtained. A garnet chert (A12E) from the mylonite zone of the Alpine Fault at Vine Creek, near Hokitika, gave a tight intersection of composition isopleths, indicating peak metamorphic conditions of 510 °C/5.5 kbar, after recalculation to correct for element fractionation by the strongly-zoned garnet. This tight, modern constraint is within error of previously-reported results from traditional geothermobarometry (420–600 °C/5.9–13 kbar) and Raman spectroscopy of carbonaceous material (RSCM T = 556 °C) from nearby sites. A peak metamorphic estimate of 520–550 °C/7–10 kbar was obtained from a dolomite-bearing sample from the garnet zone near Fox Glacier (J34), in good comparison with published temperatures from Raman spectroscopy of carbonaceous material in nearby metagreywacke samples (526–546 °C). The prograde metamorphic P–T path was probably steep, based on growth of the garnet core at ~475535 °C/5–9 kbar. The successful results for these garnet chert samples show that the new a-x models for Mn-bearing minerals extend the range of rock types that are amenable to pseudosection modelling.  Results obtained in this study also serve to highlight several possible concerns: a) garnet nucleation and initial growth in very Mn-rich rocks may be subject to local compositional or kinetic controls; b) bulk rock compositions may not always mimic the effective bulk composition; c) the existing a–x models for Mn-bearing minerals and white micas may need refining; and d) some rocks may simply be ill-suited to thermodynamic forward modelling. Items a) and b) may be indicated by the common observation of a mismatch between predicted and measured garnet composition isopleths for garnet cores, and by a mismatch between garnet composition isopleths and the appropriate mineral assemblage field for sample AMS01, from the mylonite zone, Hari Hari, Southern Alps. For item c) every P–T pseudosection calculated using the new a–x models for Mn-bearing minerals showed garnet stable to very low temperatures below 300 °C. In addition, the P–T pseudosection for an oligoclase-zone metachporphyroblasts of Fe-Ti oxides (magnetitert (Sample J36) from Hari Mare stream, Franz Josef - Fox Glacier, indicated that the white mica margarite should be present instead of plagioclase (oligoclase), for a rock in which oligoclase is present and margarite is absent, a problem previously noted elsewhere. Item d) is exemplified by a very garnet-rich ferruginous metachert sample (J35, garnet zone, headwater region, Moeraki River, South Westland) which proved impossible to model successfully due to its complex mineral growth and deformation history. This sample contained multiple generations of carbonate with differing compositions, amphibole (not incorporated for modelling with the new a–x models for Mn-bearing minerals), large e associated with smaller, possibly later-formed ilmenite), and the garnet bands were offset by late deformation.  The garnetiferous metachert samples studied here preserve in their textures and compositions clues to their growth mechanism and metamorphic history. The textures in at least two of the samples are consistent with the diffusion controlled nucleation and growth model for garnet. This research has successfully used state of the art thermodynamic modelling techniques in combination with the latest internally consistent a-x models on Mn-rich metachert, for the first time, extracting P–T conditions of the metamorphism of garnetiferous metachert from the Southern Alps.</p>


Author(s):  
Mette Olivarius ◽  
Morten Bjerager ◽  
Nynke Keulen ◽  
Christian Knudsen ◽  
Thomas F. Kokfelt

Zircon U–Pb geochronology and heavy mineral CCSEM analysis were used to interpret the provenance of Oxfordian–Volgian sandstones of the Hareelv Formation in East Greenland. Six samples were collected from the Blokelv-1 core drilled in southern Jameson Land, and the zircon age distributions and heavy-mineral assemblages are quite uniform. The samples contain a wide spectrum of Archaean to Palaeozoic zircon ages with peak ages at 2.71, 2.49, 1.95, 1.65, 1.49, 1.37, 1.10 and 0.43 Ga when combining all data. The heavy-mineral compositions show derivation from felsic source rocks, some of which were metamorphic. The results reveal that the sediment was derived from the Caledonides, and it is plausible that some or all of the material has experienced several cycles of sedimentation. Devonian and Carboniferous sediments preserved north of the area have zircon age distributions that correspond to those from the Hareelv Formation, and such rocks may have been reworked into the Jameson Land Basin. The provenance signature describes both the gravity-flow sandstones of the Hareelv Formation and the delta-edge sands that are inferred to have fed them. Lithological and provenance contrasts between the sandstones of the Sjællandselv Member and those of the Katedralen Member indicate a shorter transport distance, source to sink, suggestive of proximal topographic rejuvenation in the Volgian.


Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 252 ◽  
Author(s):  
Tarantola ◽  
Voudouris ◽  
Eglinger ◽  
Scheffer ◽  
Trebus ◽  
...  

The Trikorfo area (Thassos Island, Rhodope massif, Northern Greece) represents a unique mineralogical locality with Mn-rich minerals including kyanite, andalusite, garnet and epidote. Their vivid colors and large crystal size make them good indicators of gem-quality materials, although crystals found up to now are too fractured to be considered as marketable gems. The dominant lithology is represented by a garnet–kyanite–biotite–hematite–plagioclase ± staurolite ± sillimanite paragneiss. Thermodynamic Perple_X modeling indicates conditions of ca. 630–710 °C and 7.8–10.4 kbars. Post-metamorphic metasomatic silicate and calc-silicate (Mn-rich)-minerals are found within (i) green-red horizons with a mineralogical zonation from diopside, hornblende, epidote and grossular, (ii) mica schists containing spessartine, kyanite, andalusite and piemontite, and (iii) weakly deformed quartz-feldspar coarse-grained veins with kyanite at the interface with the metamorphic gneiss. The transition towards brittle conditions is shown by Alpine-type tension gashes, including spessartine–epidote–clinochlore–hornblende-quartz veins, cross-cutting the metamorphic foliation. Kyanite is of particular interest because it is present in the metamorphic paragenesis and locally in metasomatic assemblages with a large variety of colors (zoned blue to green/yellow-transparent and orange). Element analyses and UV-near infrared spectroscopy analyses indicate that the variation in color is due to a combination of Ti4+–Fe2+, Fe3+ and Mn3+ substitutions with Al3+. Structural and mineralogical observations point to a two-stage evolution of the Trikorfo area, where post-metamorphic hydrothermal fluid circulation lead locally to metasomatic reactions from ductile to brittle conditions during Miocene exhumation of the high-grade host-rocks. The large variety of mineral compositions and assemblages points to a local control of the mineralogy and fO2 conditions during metasomatic reactions and interactions between hydrothermal active fluids with surrounding rocks.


Sign in / Sign up

Export Citation Format

Share Document