355 resultados para Monazite.


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"February 1954."

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"January 1955."

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"April 1952."

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At head of title: Imperial Mineral Resources Bureau.

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At head of title: Imperial Mineral Resources Bureau.

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Electron microprobe (EMP) dating on monazite in granulite- facies rocks from Forefinger Point, East Antarctica, yielded dominant ages of 500 Ma on matrix monazites.They are associated with secondary cordierite, biotite and sapphirine, formed during nearly isothermal decompression after the high P-T assemblages involving garnet, orthopyroxene and sillimanite. Older ages around 750-1000 Ma are detected in monazite cores and in monazite inclusions in garnet porphyroblast. Combining the available age data and the reaction textures, it becomes evident that the Forefinger Point granulites have been overprinted by a granulite-facies decompressional event of Pan-African age. Moreover, EMP monazite dating imply that the Forefinger Point granulites have experienced at least two stages of metamorphic evolution.

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Three samples of garnet-kyanite paragneiss from the Variscan Ulten Zone (Northern Italy) were studied in detail for U-Th-Pb monazite dating. Monazite in these gneisses is abundant, shows highly variable grain size and occupies different textural positions: within the matrix, as inclusion in garnet and kyanite, within apatite aggregates. Monazite shows different deformation features as a function of the textural position: enclosed (shielded) monazite is generally more fractured than matrix (unshielded) monazite. The integration of textural information with deformation features and in situ U-Th-Pb analyses by LA-ICP-MS indicates that there is no direct correlation between textural site and monazite ages. Old ages of 351-343 Ma, determined on portions of large matrix (unshielded) monazite and on rare domains of monazite shielded by garnet, have been related to a prograde stage of the Variscan metamorphic evolution of the Ulten Zone. Ages of 330-326 Ma, which are related to the thermal peak, are recorded by small matrix monazite, external domains of large matrix monazite, and by (domains of) fractured monazite enclosed in garnet and kyanite. Large, old unshielded grains formed as blasts during the prograde metamorphic history and survived the peak metamorphism during which crystallisation/re-crystallisation partially occurred.

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Carbonatites are known to contain the highest concentrations of rare-earth elements (REE) among all igneous rocks. The REE distribution of carbonatites is commonly believed to be controlled by that of the rock forming Ca minerals (i.e., calcite, dolomite, and ankerite) and apatite because of their high modal content and tolerance for the substitution of Ca by light REE (LREE). Contrary to this conjecture, calcite from the Miaoya carbonatite (China), analyzed in situ by laser-ablation inductively-coupled-plasma mass-spectrometry, is characterized by low REE contents (100–260 ppm) and relatively !at chondrite-normalized REE distribution patterns [average (La/Yb)CN=1.6]. The carbonatite contains abundant REE-rich minerals, including monazite and !uorapatite, both precipitated earlier than the REE-poor calcite, and REE-fluorocarbonates that postdated the calcite. Hydrothermal REE-bearing !uorite and barite veins are not observed at Miaoya. The textural and analytical evidence indicates that the initially high concentrations of REE and P in the carbonatitic magma facilitated early precipitation of REE-rich phosphates. Subsequent crystallization of REE-poor calcite led to enrichment of the residual liquid in REE, particularly LREE. This implies that REE are generally incompatible with respect to calcite and the calcite/melt partition coefficients for heavy REE (HREE) are significantly greater than those for LREE. Precipitation of REE-fluorocarbonates late in the evolutionary history resulted in depletion of the residual liquid in LREE, as manifested by the development of HREE-enriched late-stage calcite [(La/Yb)CN=0.7] in syenites associated with the carbonatite. The observed variations of REE distribution between calcite and whole rocks are interpreted to arise from multistage fractional crystallization (phosphates!calcite!REE-!uorocarbonates) from an initially REE-rich carbonatitic liquid.

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The first finding of low-temperature eclogites from the Indochina region is reported. The eclogites occur along the Song Ma Suture zone in northern Vietnam, which is widely regarded as the boundary between the South China and Indochina cratons. The major lithology of the area is pelitic schist that contains garnet and phengite with or without biotite, chloritoid, staurolite and kyanite, and which encloses blocks and lenses of eclogite and amphibolite. The eclogites commonly consist of garnet, omphacite, phengite, rutile, quartz and/or epidote with secondary barroisite. Omphacite is commonly surrounded by a symplectite of Na-poor omphacite and Na-rich plagioclase. In highly retrograded domains, diopside + tremolite + plagioclase symplectites replace the primary phases. Estimated peak-pressure metamorphic conditions based on isochemical phase diagrams for the eclogites are 2.1-2.2 GPa and 600-620 degrees C, even though thermobarometric results yield higher pressure and temperature conditions (2.6-2.8 GPa and 620-680 degrees C). The eclogites underwent a clockwise P-T trajectory with a post-peak-pressure increase of temperature to a maximum of > 750 degrees C at 1.7 GPa and a subsequent cooling during decompression to 650 degrees C and 1.3 GPa, which was followed by additional cooling before close-to-isothermal decompression to similar to 530 degrees C at 0.5 GPa. The surrounding pelitic schist (garnet-chloritoid-phengite) records similar metamorphic conditions (580-600 degrees C at 1.9-2.3 GPa) and a monazite chemical age of 243 +/- 4 Ma. A few monazite inclusions within garnet and the cores of some zoned monazite in garnet-phengite schist record an older thermal event (424 +/- 15 Ma). The present results indicate that the Indochina craton was deeply (> 70 km) subducted beneath the South China craton in the Triassic. The Silurian cores of monazite grains may relate to an older non-collisional event in the Indochina craton.

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The Palu Metamorphic Complex (PMC) is exposed in a late Cenozoic orogenic belt in NW Sulawesi, Indonesia. It is a composite terrane comprising a gneiss unit of Gondwana origin, a schist unit composed of meta-sediments deposited along the SE Sundaland margin in the Late Cretaceous and Early Tertiary, and one or more slivers of amphibolite with oceanic crust characteristics. The gneiss unit forms part of the West Sulawesi block underlying the northern and central sections of the Western Sulawesi Province. The presence of Late Triassic granitoids and recycled Proterozoic zircons in this unit combined with its isotopic signature suggests that the West Sulawesi block has its origin in the New Guinea margin from which it rifted in the late Mesozoic. It docked with Sundaland sometime during the Late Cretaceous. U–Th–Pb dating results for monazite suggest that another continental fragment may have collided with the Sundaland margin in the earliest Miocene. High-pressure (HP) and ultrahigh-pressure (UHP) rocks (granulite, peridotite, eclogite) are found as tectonic slices within the PMC, mostly along the Palu–Koro Fault Zone, a major strike-slip fault that cuts the complex. Mineralogical and textural features suggest that some of these rocks resided at depths of 60–120 km during a part of their histories. Thermochronological data (U–Th–Pb zircon and 40Ar/39Ar) from the metamorphic rocks indicate a latest Miocene to mid-Pliocene metamorphic event, which was accompanied by widespread granitoid magmatism and took place in an extensional tectonic setting. It caused recrystallization of, and new overgrowths on, pre-existing zircon crystals, and produced andalusite–cordierite–sillimanite–staurolite assemblages in pelitic protoliths, indicating HT–LP (Buchan-type) metamorphism. The PMC was exhumed as a core complex at moderate rates (c. 0.7–1.0 mm/yr) accompanied by rapid cooling in the Plio-Pleistocene. Some of the UHP rocks were transported to the surface at significantly higher rates (⩾16 mm/yr). The results of our study do not support recent plate tectonic reconstructions that propose a NW Australia margin origin for the West Sulawesi block (e.g. Hall et al., 2009).

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Leucogranite magmatism occurred in southern Finland during the later stages of the Paleoproterozoic Svecofennian orogeny. The leucogranites are considered to have formed from pre-existing crustal rocks that have undergone anatexis in the extensional stage of the orogeny, following continental collision and resultant crustal thickening. The leucogranites have been studied in the field using petrographic and mineralogical methods, elemental and isotope geochemistry on whole rocks and minerals, and U-Pb geochronology. On outcrop scale, these granites typically form heterogeneous, layered, sheet-like bodies that migmatize their country rocks. All of the leucogranites are peraluminous and rich in SiO2, but otherwise display significant geochemical variation. Their Nd isotope composition ranges from fairly juvenile to very unradiogenic, and the Hf isotope composition of their zircon shows a varying degree of mixing in the source, the zircon populations becoming more heterogeneous and generally less radiogenic towards the east. The leucogranites have been dated using U-Pb isotopic analyses, utilizing thermal ionization mass spectrometry, secondary ion mass spectrometry, and laser ablation multicollector ICP mass spectrometry on zircon and monazite. The results show that the granites were emplaced between 1.85 Ga and 1.79 Ga, which is a considerably longer period than has traditionally been perceived for these rocks. The rocks tend to become younger towards the east. Single crystal data also display a wide array of inherited zircons, especially in the eastern part of the leucogranite belt. The most common inherited age groups are ~2.8 2.5 Ga, ~2.1 2.1 Ga, and ~1.9 Ga. Magmatic zircon and monazite usually record similar ages for any one sample.Thermobarometric calculations indicate that the leucogranites in the Veikkola area of southcentral Finland were formed from relatively low-temperature melts, and emplaced at 17-25 km depth, i.e. at mid-crustal level. It is likely that these conditions apply to the Svecofennian leucogranites in general. Large differences in the Hf and Nd isotope compositions, emplacement ages, and distributions of inherited zircon ages show that these granites were formed from different types of source rocks, which probably included both sedimentary and igneous rocks.

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Ultrahigh-temperature (UHT) granulites of the central Highland Complex, Sri Lanka, underwent some of the highest known peak temperatures of crustal metamorphism. Zircon and monazite U-Pb systems in granulites near Kandy, the highest grade region (similar to 1050 degrees C; 0.9 GPa), preserve both a record of the timing of prograde and retrograde phases of UHT metamorphism and evidence for the ages of older protolith components. Zircon grains from a quartz-saturated granulite containing relics of the peak UHT assemblage have remnant detrital cores with dates of ca. 2.5-0.83 Ga. Date clusters of ca. 1.7 and 1.04-0.83 Ga record episodes of zircon growth in the source region of the protolith sediment. Two generations of overgrowths with contrasting Th/U record metamorphic zircon growth at 569 +/- 5 and 551 +/- 7 Ma, probably in the absence and presence of monazite, respectively. The age of coexisting metamorphic monazite (547 +/- 7 Ma) is indistinguishable from that of the younger, low-Th/U zircon overgrowths. Zircon from a quartz-undersaturated monazite-absent UHT granulite with a mainly retrograde assemblage is mostly metamorphic (551 +/- 5 Ma). The ca. 570 Ma zircon overgrowths in the quartz-saturated granulite probably record partial melting just before or at the metamorphic peak. The ca. 550 Ma zircon in both rocks, and the ca. 550 Ma monazite in the quartz-saturated sample, record post-peak isothermal decompression. A possible model for this pressure-temperature-time evolution is ultrahot collisional orogeny during the assembly of Gondwana, locally superheated by basaltic underplating, followed by fast extensional exhumation.

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Sapphirine-cordierite intergrowths occur as pods within garnet-absent, high-Mg orthopyroxene-granulite xenoliths in the Kambam valley, Madurai Block, southern India. Whereas the cores of the pods are composed of sapphirine (X-Mg = 0.871-0.897) - cordierite (X-Mg = 0.892-0.931) intergrowth along with rutile, zircon and monazite, the rims are characterized by cordierite, apatite, plagioclase, K-feldspar, quartz and minor calcite. The surrounding matrix comprises orthopyroxene (maximum Al2O3 4.1 wt.%, X-Mg 0.848-0.850), plagioclase, biotite and quartz, similar to the assemblage in the surrounding charnockites. Sapphirine in the Kambam rocks is characterized by high Al contents with an end-member composition in the range of 7:9:3 and 3:5:1. The occurrence of peraluminous sapphirine in association with cordierite and in the absence of phases such as sillimanite and garnet is distinct from ultrahigh-temperature assemblages in other localities within the Madurai Block. The peraluminous composition of the pods suggests that these domains could represent cryptic pathways through which aluminous melts migrated. The reaction of such peraluminous melts with Mg-rich orthopyroxene in the host granulite at temperatures of 1025 degrees C and pressures around 8 kbar as computed from phase equilibria modeling followed by an isobaric cooling is inferred to have generated the sapphirine-cordierite pods. The unusual high-Mg orthopyroxene granulite suggests interaction of supracrustal rocks with mafic magmas, which probably acted as the heat source for the partial melting of lower crust and UHT metamorphism.

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O Domínio Costeiro integra o Terreno Oriental, no segmento central da Faixa Ribeira e abriga rochas ortoderivadas com afinidade de arcos magmáticos (Complexo Rio Negro, ca. 790-605 Ma). Os ortognaisses deste complexo possuem clara assinatura para ambientes de zonas de subducção, encaixados em rochas metassedimentares de alto grau, integrantes do Grupo São Fidélis. O conjunto acima descrito é ainda intrudido por várias de rochas granitóides sin a tardi- colisionais, relacionadas às várias etapas de desenvolvimento da Orogenia Brasiliana neste setor do orógeno (ca. 605-480 Ma). Idades U-Pb (LA-ICP-MS) em zircões detríticos de rochas quartzíticas do Grupo São Fidélis indicam um amplo espectro com modas significativas no Mesoproterozóico e Paleoproterozoico, além de zircões do Neoproterozóico e do Arqueano. Sinteticamente os resultados obtidos foram: a) Idades concordantes Arqueanas com ca. 2,85, 2,84 e 2,70 Ga; b) zircões Paleoproterozóicos (ca. 2,3 a 1,7 Ga), com máxima concentração em torno de ca. 2,2 Ga, representando a segunda maior moda; c) Idades Mesoproterozóicas (ca. 1,3 -1,1 Ga) com idades de espectro dominantes, com moda em ca. 1,5 Ga; d) Zircões Neoproterozóicos com idades de ca. 0,95-90 Ga e 0,86-0,61 Ga. Em vários grãos detríticos observou-se sobrecrescimento metamórfico em ca. 602-570 Ma. Dados U-Pb (LA-ICP-MS) obtidos para zircões para Ortognaisse Rio Grande e o Biotita Ortognaisse, intrudidos na unidade basal do Grupo São Fidélis, apresentam idades em ca. 620 Ma e são equivalentes ao período pré-colisional de geração de rochas do arco magmático Rio Negro. Combinando estas idades com os núcleos de zircões detríticos mais jovens, com assinatura do Arco Rio Negro em ca. 613 Ma, pode-se definir o intervalo máximo de sedimentação da unidade superior do Grupo São Fidélis no Neoproterozóico. Cristais de monazitas selecionadas para análise U-Pb (ID-TIMS) apresentam relações com os principais episódios tectono-metamórficos da Faixa Ribeira. Dois cristais de uma amostra quartzítica e dois do ortognaisse Rio Grande alinham-se em uma discórdia que gerou idade de 603 Ma, referente ao metamorfismo progressivo descrito na literatura, durante a Orogenia Brasiliana. Enquanto a idade concordante obtida em 535 Ma, adquirida em uma amostra quartzítica, é correspontente ao último metamorfismo colisional da Faixa Ribeira.

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Os elementos de terras raras, representados em sua maioria pelos lantanídeos, ocorrem principalmente como constituintes-traço da maioria dos minerais de rochas comuns (monazita, apatita) e também estão presentes em alguns minérios. Tais elementos foram largamente usados por décadas como fertilizantes na China. Na área das inovações tecnológicas, a demanda por esses metais vem crescendo por conta das suas aplicações em diversos campos. Consequentemente, grandes quantidades desses elementos são acumulados em ambientes aquáticos atingindo o fitoplâncton. Assim, as microalgas que são organismos ecologicamente importantes na cadeia alimentar têm sido frequentemente usadas em estudos ambientais para avaliar a toxicidade relativa de várias descargas químicas e são largamente estudadas na detecção dos primeiros impactos no ecossistema. Somado a isso, são biomassas que possuem boa capacidade de biossorção de metais devido à presença de ligantes na sua estrutura que promovem a captação deles quando em solução. Dessa forma, as interações entre as microalgas verdes Monoraphidium e Scenedesmus e os íons La3+ e Ce3+ foram investigadas neste trabalho. Para isso, foram avaliados o efeito tóxico e a bioacumulação do La3+ pelas duas microalgas verdes. Adicionalmente, estudos em batelada da biossorção do La3+ e Ce3+ em soluções contendo os elementos isoladamente ou em combinação foram realizados. No estudo de toxicidade e de bioacumulação o meio de cultivo utilizado foi o ASM-1, com e sem presença de La3+ (10 mg.L-1 a 100 mg.L-1), onde o efeito tóxico do metal foi monitorado por análises micro e macroscópica das células e também pela quantificação do crescimento celular baseada em medidas da massa seca. A bioacumulação do metal foi avaliada da mesma forma para ambas as microalgas. Os resultados obtidos mostraram que o efeito tóxico do metal foi presente em concentrações iônicas de 50 e 100 mg.L-1 e que houve uma bioconcentração do La3+ em ambas espécies de microalgas, principalmente quando a concentração inicial do La3+ foi de 10 e 25 mg.L-1, mostrando que houve uma relação direta entre a bioconcentração e a toxicidade do La3+. O gênero Monoraphidium bioconcentrou mais metal que o gênero Scenedesmus. Os resultados da biossorção dos metais em solução monoelementar mostraram que as microalgas apresentaram grande capacidade de captação do La3+ (20,7 mmol.g-1 para Monoraphidium sp. e 17,8 mmol.g-1 para Scenedesmus sp.) e do Ce3+ (25,7 mmol.g-1 para Monoraphidium sp. e 11,5 mmol.g-1 para Scenedesmus sp.). Os resultados obtidos revelaram que os dados melhor se ajustaram ao modelo de Freundlich, na maioria dos casos. Em sistema binário, notou-se que houve uma menor captação de cada um individualmente, evidenciando uma competição entre eles pelos mesmos sítios ligantes e que ambas apresentaram maior afinidade pelo Ce3+