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241.
Normal grain growth of calcite was investigated by combining grain size analysis of calcite across the contact aureole of the Adamello pluton, and grain growth modeling based on a thermal model of the surroundings of the pluton. In an unbiased model system, i.e., location dependent variations in temperature-time path, 2/3 and 1/3 of grain growth occurs during pro- and retrograde metamorphism at all locations, respectively. In contrast to this idealized situation, in the field example three groups can be distinguished, which are characterized by variations in their grain size versus temperature relationships: Group I occurs at low temperatures and the grain size remains constant because nano-scale second phase particles of organic origin inhibit grain growth in the calcite aggregates under these conditions. In the presence of an aqueous fluid, these second phases decay at a temperature of about 350 °C enabling the onset of grain growth in calcite. In the following growth period, fluid-enhanced group II and slower group III growth occurs. For group II a continuous and intense grain size increase with T is typical while the grain growth decreases with T for group III. None of the observed trends correlate with experimentally based grain growth kinetics, probably due to differences between nature and experiment which have not yet been investigated (e.g., porosity, second phases). Therefore, grain growth modeling was used to iteratively improve the correlation between measured and modeled grain sizes by optimizing activation energy (Q), pre-exponential factor (k0) and grain size exponent (n). For n=2, Q of 350 kJ/mol, k0 of 1.7×1021 mns–1 and Q of 35 kJ/mol, k0 of 2.5×10-5 mns–1 were obtained for group II and III, respectively. With respect to future work, field-data based grain growth modeling might be a promising tool for investigating the influences of secondary effects like porosity and second phases on grain growth in nature, and to unravel differences between nature and experiment.Editorial responsibility: J. Hoefs  相似文献   
242.
A massif-type (intrusive) charnockite body in the Eastern Ghats granulite belt, India, is associated with hornblende-bearing mafic granulite, two-pyroxene granulite and enderbitic granulite. The charnockite is characterised by pervasive gneissic foliation (S1). This is axial planar to the folded layers of hornblende-bearing mafic granulite (F1 folds), indicating that the granulite protoliths were present before the development of S1. Two-pyroxene granulite and enderbitic granulite occur as lenticular patches disposed along the foliation and hence could be syngenetic to S1. The tonalitic to granodioritic, metaluminous to weakly peraluminous compositions and relatively high Sr/Rb of the charnockite are consistent with its derivation by partial melting of a mafic protolith. Strong Y depletion, lack of Sr depletion and strongly fractionated REE patterns with high (La/Yb)N ratio, but relatively lower HREE (Gd/Lu) fractionation with marked positive Eu anomalies, suggest major residual hornblende (as well as garnet), but not plagioclase, consistent with the hornblende dehydration melting in the source rocks. Such a residual mineralogy is broadly similar to those of some of the hornblende-bearing mafic granulite inclusions, which have compositional features indicative of a restitic nature. Quantitative modelling supports an origin for the charnockite melts by partial melting of a hornblende-rich mafic granulite source, although source heterogeneity is very likely given the rather variable trace element contents of the charnockite. The whole-rock and mineral compositions of the two-pyroxene granulites and enderbitic granulites are consistent with them representing peritectic phase segregations of hornblende-dehydration melting. A clockwise P-T path implies that melting could have occurred in thickened continental crust undergoing decompression.Editorial responsibility: T.L. Grove  相似文献   
243.
Biotite is one of the most common minerals dated by the 40Ar–39Ar method. It frequently shows K contents below the expected stoichiometric value, suggesting the presence of low-K impurities. The most common low-K alteration product of biotite is chlorite. Therefore, it is important to understand the effects of chlorite interlayering on 40Ar–39Ar ages in order to correctly interpret 40Ar–39Ar data. This study examines the outcome of 40Ar–39Ar dating analyses on variably chloritised biotites from Ordovician intrusive rocks. The infrared (IR) laser-probe technique and different gas extraction methods were adopted. Incremental laser-heating data on bulk samples yielded hump-shaped age profiles with meaningless young and old age steps. Both the extent of anomalous old age steps and the degree of discordance of the age spectra were much more pronounced in the more chloritised biotite samples. In contrast, in situ data on rock chips and total-fusion ages on single biotite flakes yielded ages concordant with, or younger than, the inferred emplacement ages. Transmission electron microscopy (TEM) was used to texturally characterise biotite samples at the nanometre scale. It was also used to document the complex decomposition-transformation process affecting interlayered biotite–chlorite during in-vacuo IR-laser heating to temperatures ranging from ~600 to >1,000 °C. TEM results suggest that hump-shaped age profiles result from an interplay between 39ArK redistribution by recoil during sample irradiation and differential release of argon isotopes hosted in three main reservoirs. These reservoirs are (from least to most retentive): extended defects, chlorite and biotite. The final descending age segment is attributed to the progressive release of argon with increasing temperature from large biotite domains for which 39ArK recoil loss was less important. 40Ar–39Ar data support previous findings, which suggest that 40Ar–39Ar ages when recoil effects are minimised, provide minimum estimates that approach the true biotite age, when the pristine domains are analysed. The most effective approach for obtaining meaningful 40Ar–39Ar ages was using individual total-fusion analyses on carefully selected, single flakes previously split along the basal cleavage by wet-grinding and corresponding to a sample mass of a few micrograms.Editorial responsibility: I Parsons  相似文献   
244.
We have investigated the near liquidus phase relations of a primitive absarokite from the Mascota region in western Mexico. Sample M.102 contains ~11.6 wt% MgO, Mg#=0.73 and the lava contains Fo90 olivine phenocrysts, indicating near equilibrium with the mantle. High-pressure experiments on a synthetic analogue of the absarokite composition containing low and high H2O abundances of (~2 and ~5 wt%, respectively) were performed in a piston cylinder apparatus over the pressure range of 1.2 to 2.0 GPa. The composition containing ~2 wt% H2O is multiply saturated with olivine and orthopyroxene at 1.6 GPa and 1,400 °C. At the same pressure, clinopyroxene appears 30 °C below the liquidus. At an H2O content of ~5 wt% the multiple saturation with olivine and orthopyroxene occurs at 1.7 GPa and 1,300 °C. Assuming a batch-melting process, we suggest that the primitive absarokite was segregated from a depleted lherzolite or harzburgite residue at ~50 km, placing the depth of origin well within the mantle wedge beneath the Jalisco Block. A low degree (<5 %wt%) batch-melt of an original metasomatized depleted lherzolite or harzburgite source would contain the observed trace element abundances found in M.102. The liquidus phase relations are not consistent with the presence of non-peridotitic veins at the depth of last equilibration. Therefore, we propose that the Mascota absarokites segregated at an apparent melt fraction of less than 5% from a depleted peridotitic source. Melting first began at a greater depth as a small degree H2O- and trace element- rich melt of a metasomatized peridotite that ascended into the overlying wedge and re-equilibrated with shallower, hotter mantle.Editorial responsibility: J. Hoefs  相似文献   
245.
Rb–Sr isotope data for siderite and fluorite from sediment-hosted epithermal mineral veins in the eastern Harz Mountains (Germany) are presented. Several fluorite and siderite-bearing paragenetic stages have been proposed for these veins, with the most important mineralization being related to a quartz–sulfide and a subsequent calcite–fluorite–quartz stage, which occurred at 226±1 and 209±2 Ma, respectively. Our Rb–Sr data do not permit the identification of distinct generations of siderite and fluorite, but rather reveal straight internal mixing relations, reflecting mixing of fluids or differential fluid–rock interaction processes. This indicates merely two significant phases of mineral deposition related to the quartz–sulfide and calcite–fluorite–quartz stages. It is shown that the Paleozoic sedimentary host rocks of the veins are the most likely source for the siderite Sr, whereas fluorite displays a two-component mixture between sedimentary Sr and radiogenic Sr derived from locally occurring Permian metavolcanic rocks. Editorial handling: B. Lehmann  相似文献   
246.
Adakite-like features are recognized in the Late Miocene (~10 Ma) porphyritic intrusions of the Los Pelambres giant porphyry copper deposit, central Chile (32°S). Located within the southern portion of the flat-slab segment (28–33°S) of the Chilean Andes, the Al- and Na-rich porphyries of Los Pelambres display distinctly higher Sr/Y (~100–300) and LaN/YbN (~25–60) ratios than contemporaneous and barren magmatic units (e.g., La Gloria pluton, Cerro Aconcagua volcanic rocks) of the same Andean magmatic belt. Strong fractionation of heavy rare earth elements (HREE), absence of Eu anomalies, high Sr/Y and Zr/Sm and low Nb/Ta ratios suggest melt extraction from a garnet-amphibolite source. The Late-Miocene adakite-like porphyritic intrusions at Los Pelambres formed closely related in time and space to the subduction of the Juan Fernández Ridge (JFR) hotspot chain along the Chilean margin. Current tectonic reconstructions reveal that, at the time of formation of the Los Pelambres rocks, a W-E segment of the JFR started to subduct beneath them, producing a slow-down of a previously rapid southward migration of a NE-ridge—trench collision. These particular tectonic conditions are favorable for the origin of the Los Pelambres porphyry suite by melting of subducting young hotspot rocks under flat-slab conditions. The incorporation of crustal components into the oceanic lithopheric magma source by subduction erosion is evidenced by the Sr-Nd isotope composition of the Los Pelambres rocks different from the MORB signatures of true adakites. A close relationship apparently exists between the origin of this adakite-like magmatism and the source of the mineralization in the Los Pelambres porphyry copper deposit.Editorial handling: R.J. Goldfarb  相似文献   
247.
The world-class Idrija mercury deposit (western Slovenia) is hosted by highly deformed Permocarboniferous to Middle Triassic sedimentary rocks within a complex tectonic structure at the transition between the External Dinarides and the Southern Alps. Concordant and discordant mineralization formed concomitant with Middle Triassic bimodal volcanism in an aborted rift. A multiple isotopic (C, O, S) investigation of host rocks and ore minerals was performed to put constraints on the source and composition of the fluid, and the hydrothermal alteration. The distributions of the 13C and 18O values of host and gangue carbonates are indicative of a fracture-controlled hydrothermal system, with locally high fluid-rock ratios. Quantitative modeling of the 13C and 18O covariation for host carbonates during temperature dependent fluid-rock interaction, and concomitant precipitation of void-filling dolomites points to a slightly acidic hydrothermal fluid (13C–4 and 18O+10), which most likely evolved during isotopic exchange with carbonates under low fluid/rock ratios. The 34S values of hydrothermal and sedimentary sulfur minerals were used to re-evaluate the previously proposed magmatic and evaporitic sulfur sources for the mineralization, and to assess the importance of other possible sulfur sources such as the contemporaneous seawater sulfate, sedimentary pyrite, and organic sulfur compounds. The 34S values of the sulfides show a large variation at deposit down to hand-specimen scale. They range for cinnabar and pyrite from –19.1 to +22.8, and from –22.4 to +59.6, respectively, suggesting mixing of sulfur from different sources. The peak of 34S values of cinnabar and pyrite close to 0 is compatible with ore sulfur derived dominantly from a magmatic fluid and/or from hydrothermal leaching of basement rocks. The similar stratigraphic trends of the 34S values of both cinnabar and pyrite suggest a minor contribution of sedimentary sulfur (pyrite and organic sulfur) to the ore formation. Some of the positive 34S values are probably derived from thermochemical reduction of evaporitic and contemporaneous seawater sulfates.Editorial handling: P. Lattanzi  相似文献   
248.
Large subvolcanic intrusions are recognized within most Precambrian VMS camps. Of these, 80% are quartz diorite–tonalite–trondhjemite composite intrusions. The VMS camps spatially associated with composite intrusions account for >90% of the aggregate sulfide tonnage of all the Precambrian, intrusion-related VMS camps. These low-alumina, low-K, and high-Na composite intrusions contain early phases of quartz diorite and tonalite, followed by more voluminous trondhjemite. They have a high proportion of high silica (>74% SiO 2) trondhjemite which is compositionally similar to the VMS-hosting rhyolites within the volcanic host-rock successions. The quartz-diorite and possibly tonalite phases follow tholeiitic fractionation trends whereas the trondhjemites fall within the composition field for primitive crustal melts. These transitional M-I-type primitive intrusive suites are associated with extensional regimes within oceanic-arc environments. Subvolcanic composite intrusions related to the Archean Sturgeon Lake and Noranda, and Paleoproterozoic Snow Lake VMS camps range in volume from 300 to 1,000 km 3. Three have a sill morphology with strike lengths between 15 and 22 km and an average thickness between 1,500 and 2,000 m. The fourth has a gross stock-like shape. The VMS deposits are principally restricted to the volcanic strata above the strike length of the intrusions, as are areally extensive, thin exhalite units. The composite intrusions contain numerous internal phases which are commonly clustered within certain parts of the composite intrusion. These clusters underlie eruptive centers surrounded by areas of hydrothermal alteration and which contain most of the VMS deposits. Early quartz-diorite and tonalite phases appear to have intruded in rapid succession. Evidence includes gradational contacts, magma mixing and disequilibrium textures. They appear to have been emplaced as sill-dike swarms. These early phases are present as pendants and xenoliths within later trondhjemite phases. The trondhjemite phases contain numerous internal contacts indicating emplacement as composite sills. Common structural features of the composite intrusions include early xenolith phases, abundant small comagmatic dikes, fractures and veins and, in places, columnar jointing. Internal phases may differ greatly in texture from fine- to coarse-grained, aphyric and granophyric through seriate to porphyritic. Mineralogical and isotopic evidence indicates that early phases of each composite intrusion are affected by pervasive to fracture-controlled high-temperature (350–450 °C) alteration reflecting seawater-rock interaction. Trondhjemite phases contain hydrothermal-magmatic alteration assemblages within miarolitic cavities, hydrothermal breccias and veins. This hydrothermal-magmatic alteration may, in part, be inherited from previously altered wall rocks. Two of the four intrusions are host to Cu-Mo-rich intrusive breccias and porphyry-type mineralization which formed as much as 14 Ma after the main subvolcanic magmatic activity. The recognition of these Precambrian, subvolcanic composite intrusions is important for greenfields VMS exploration, as they define the location of thermal corridors within extensional oceanic-arc regimes which have the greatest potential for significant VMS mineralization. The VMS mineralization may occur for 2,000 m above the intrusions. In some cases, VMS mineralization has been truncated or enveloped by late trondhjemite phases of the composite intrusions. Evidence that much of the trondhjemitic magmatism postdates the principal VMS activity is a critical factor when developing heat and fluid flow models for these subseafloor magmatic-hydrothermal systems.  相似文献   
249.
The Late Archean Blake River Group is a thick succession of predominantly mafic volcanic rocks within the southern zone of the Abitibi greenstone belt. It contains a number of silicic volcanic centers of different size, including the large Noranda volcanic complex, which is host to 17 past-producing volcanogenic massive sulfide deposits. The Noranda complex consists of a 7- to 9-km-thick succession of bimodal mafic and felsic volcanic rocks erupted during five major cycles of volcanism. Massive sulfide formation coincided with a period of intense magmatic activity (cycle III) and the formation of the Noranda cauldron. Hydrothermal alteration in these rocks is interpreted to reflect large-scale hydrothermal fluid flow associated with rapid crustal extension and rifting of the volcanic complex. The alteration includes abundant albite, chlorite, epidote and quartz (silicification), which exhibit broad stratigraphic and structural control and correlate with previously mapped whole-rock oxygen isotope zonation. The Mine Sequence volcanic rocks are characterized by abundant iron-rich chlorite (Fe/Fe+Mg >0.5), hydrothermal amphibole (ferroactinolite) and coarse-grained epidote of clinozoisite composition (<10 wt% Fe 2O 3). Volcanic rocks of the pre-cauldron sequences, which contain only subeconomic stringer mineralization, are characterized by less abundant chlorite and mainly fine-grained epidote (>10 wt% Fe 2O 3) lacking the clinozoisite solid solution. Alteration in the Mine Sequence volcanic rocks persists along strike well beyond the limits of the main ore deposits (as far as several tens of kilometers) and can be readily distinguished from greenschist facies metamorphic assemblages at a regional scale. The lack of similar alteration in the pre-cauldron sequences is consistent with limited 18O-depletion and suggests that the early history of the volcanic complex did not support large-scale, high-temperature fluid flow in these rocks. Comparisons with a much smaller, barren volcanic complex in nearby Ben Nevis township reveal important differences in the alteration mineralogy between volcanoes of different size, with implications for area selection during regional-scale mineral exploration. The Ben Nevis Complex consists of a 3- to 4-km-thick succession of mafic, intermediate and felsic volcanic rocks centered on a small subvolcanic intrusion. Alteration of the volcanic rocks comprises mainly low-temperature assemblages of prehnite, pumpellyite, magnesium-rich chlorite (Fe/Fe+Mg <0.5), iron-rich epidote (>10 wt% Fe 2O 3) and calcite. Actinolite ± magnetite alteration occurs proximal to the intrusive core of the complex, but the limited extent of this alteration indicates only local high-temperature fluid circulation adjacent to the intrusion. A distal zone of carbonate alteration is located 4–6 km from the center of the volcano. Although iron-bearing carbonates are present locally within this zone, the absence of siderite argues against a high-temperature origin for this alteration. These observations do not offer positive encouragement for the existence of a fossil geothermal system of sufficient size or intensity to have produced a large massive sulfide deposit.  相似文献   
250.
The Ransko gabbro-peridotite massif in Eastern Bohemia is a strongly differentiated intrusive complex of Lower Cambrian age. The complex hosts low grade Ni-Cu ores mainly developed close to the contact of olivine-rich rocks with gabbros, in troctolites and, to a much lesser extent, in both pyroxene and olivine gabbros and plagioclase-rich peridotites. The ore zone is characterized by strong serpentinization and uralitization. The total Ni + Cu locally reaches up to 4 wt%. Anomalous concentrations of platinum-group elements (PGE's) (maximum 532 ppb Pd, 182 ppb Pt, 53 ppb Rh, 15 ppb Ru, 41 ppb Ir) were detected in samples of Cu-Ni and Ni-Cu ores (maximum 2.63 wt% Ni and 2.31 wt% Cu) from the Jezírka orebody. The main ore paragenesis includes pyrrhotite, pentlandite, chalcopyrite, cubanite, pyrite, magnetite, mackinawite, valleriite, ilmenite and sphalerite. During this work, michenerite, froodite, sperrylite, gold, native bismuth, altaite, tsumoite, hessite, an unnamed Bi-Ni telluride, cobaltite-gersdorffite and galena were newly identified. The host rocks originated through partial melting of a slightly depleted mantle source with noble metals scavenged from this primitive magma prior to the development of these rocks.  相似文献   
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