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1.
Major and trace elemental concentrations as well as Sr and Pb isotopic data, obtained for 41 plutonic samples from the Coast Mountains Batholith ranging in age from ～108 to ～50 Ma, indicate that the source regions for these rocks were relatively uniform and typical of Cordilleran arcs. The studied rocks are mineralogically and chemically metaluminous to weakly peraluminous and are mainly calc-alkaline. Initial whole-rock 87Sr/86Sr ratios range from 0.7035 up to 0.7053, whereas lead isotopic data range from 18.586 to 19.078 for 206Pb/204Pb, 15.545 to 15.634 for 207Pb/204Pb, and 37.115 to 38.661 for 208Pb/204Pb. In contrast to these relatively primitive isotopic data, δ 18O values for quartz separates determined for 19 of the samples range from 6.8 up to 10.0‰. These δ 18O values preclude the possibility that these melts were exclusively generated from the Mesozoic mantle wedge of this continental arc, just as the Sr and Pb data preclude significant involvement of an old (Precambrian) crustal/mantle lithospheric source. We interpret the high δ 18O component to represent materials that had a multi-stage crustal evolution. They were originally mafic rocks derived from a circum-Pacific juvenile mantle wedge that experienced a period of near-surface residence after initial crystallization. During this interval, these primitive rocks interacted with meteoric waters at low temperatures, as indicated by the high δ 18O values. Subsequently, these materials were buried to lower crustal depths where they remelted to form the high δ 18O component of the Coast Mountains Batholith. This component makes up at least 40% (mass) of the Cretaceous through Eocene batholith in the studied area. The remainder of the source materials comprising the Coast Mountains Batholith had to be new additions from the mantle wedge. A prolonged period of contractional deformation beginning with the Early Cretaceous collisional accretion of the Insular superterrane is inferred to have been responsible for underthrusting the high δ 18O component into the lower crust. We suggest that mafic rocks of the Insular superterrane (e.g. Alexander–Wrangellia) are of appropriate composition, and were accreted to and overthrust by what would become the Coast Mountains Batholith just prior to initiation of magmatism in the region.  相似文献   

2.
This paper investigates the origin of low-δ18O quartz porphyry dykes associated with the 144–133 Ma Koegel Fontein Igneous Complex, which was intruded during the initial phase of breakup of Africa and South America. The 25-km diameter Rietpoort Granite is the largest and youngest phase of activity, and is roofed by a 10-km diameter pendant of gneiss. Quartz porphyry (QP) dykes, up to 15 m in width, strike NW–SE across the complex. The QP dykes that intruded outside the granite have similar quartz phenocryst δ18O values (average 8.0‰, ± 0.7, n?=?33) to the granite (average 8.3?±?1.0, n?=?7). The QP dykes that intruded the roof pendant have quartz phenocrysts with more variable δ18O values (average 1.6‰, ± 2.1, n?=?55). In some cases quartz phenocrysts have δ18O values as low as ? 2.5‰. The variation in δ18O value within the quartz crystal population of individual dykes is small relative to the overall range, and core and rim material from individual quartz phenocrysts in three samples are identical within error. There is no evidence that quartz phenocryst δ18O values have been affected by fluid–rock interaction. Based on a ?quartz?magma value of 0.6‰, magma δ18O values must have been as low as ? 3.1‰. Samples collected along the length of the two main QP dykes that traverse the roof pendant have quartz phenocryst δ18O values that range from +?1.1 to +?4.6‰, and ? 2.3 to +?5.6‰, respectively. These δ18O values correlate negatively (r = ? 0.96) with initial 87Sr/86Sr, which can be explained by the event that lowered δ18O values of the source being older than the dykes. We suggest that the QP dykes were fed by magma produced by partial melting of gneiss, which had been variably altered at high temperature by 18O-depleted meteoric water during global glaciation at ~?550 Ma. The early melts had variable δ18O value but as melt pockets interconnected during melting, the δ18O values approached that of average gneiss. Variable quartz phenocryst δ18O values in the same dyke can be explained by vertical emplacement, at variable rates of ascent along the dyke. The lateral variation in quartz, and hence magma δ18O value at a particular point along a single dyke would depend on the rate of ascent of magma at that point along the dyke, and the ‘age’ of the particular magma batch.  相似文献   

3.
Stable carbon and oxygen isotope measurements have been obtained from ten calcareous soil profiles developed on noncalcareous parent materials in Nevada and New Mexico. Despite the number of variables that can affect the isotopic composition of soil carbonate, most of these profiles show remarkably little variation in δ 13C and δ 18O with depth. This tendency towards uniformity is attributed to the fact that pedogenic carbonate forms by the incremental accumulation of a large number of small aliquots of CaCO3. As the number of aliquots of CaCO3 increases, the composition of their sum, which is the calcareous horizon itself, tends to converge to the long-term average of the individual aliquots. A mathematical model is presented to show how the time required for convergence is affected by the amplitude and period of aliquot variation and the extent of dissolution and reprecipitation of previously deposited carbonate. Calculations further indicate that in some cases the variation in δ 18O of soil carbonates may be moderated by the opposing effects of temperature change on the H2OCaCO3 fractionation factor and on the extent of evapotranspiration.The data of this study indicate that soil carbonates from sites within a homogeneous climatic region show relatively little site-to-site variation in δ 18O as compared to geographical variation in δ 13C. This suggests that the δ 18O of soil carbonates is primarily controlled by broad climatic factors (rainfall composition and temperature) whereas site factors (e.g., soil CO2) have a strong effect on δ 13C. In Nevada and New Mexico the δ 18O of Pleistocene calcareous profiles is 2.0–4.0‰ lighter than that of nearby Holocene soil carbonate, suggesting that old well-developed profiles may have formed dominantly under cooler pluvial conditions.  相似文献   

4.
 Late Proterozoic to Cambrian carbonate rocks from Lone Mountain, west central Nevada, record multiple post-depositional events including: (1) diagenesis, (2) Mesozoic regional metamorphism, (3) Late Cretaceous contact metamorphism, related to the emplacement of the Lone Mountain granitic pluton and (4) Tertiary hydrothermal alteration associated with extension, uplift and intrusion of silicic porphyry and lamprophyre dikes. Essentially pure calcite and dolomite marbles have stable isotopic compositions that can be divided into two groups, one with positive δ13C values from+3.1 to +1.4 ‰ (PDB) and high δ18O values from +21.5 to +15.8 ‰ (SMOW), and the other with negative δ13C values from –3.3 to –3.6‰ and low δ18O values from +16.9 to +11.1‰. Marbles also contain minor amounts of quartz, muscovite and phlogopite. Brown and blue luminescent, clear, smooth textured quartz grains from orange luminescent calcite marbles have high δ18O values from +23.9 to +18.1‰, while brown luminescent, opaque, rough textured quartz grains from red luminescent dolomite marbles typically have low δ18O values from +2.0 to +9.3‰. The δ18O values of muscovite and phlogopite from marbles are typical of micas in metamorphic rocks, with values between +10.4 and +14.4‰, whereas mica δD values are very depleted, varying from −102 to −156‰. No significant lowering of the δ18O values of Lone Mountain carbonates is inferred to have occurred during metamorphism as a result of devolatilization reactions because of the essentially pure nature of the marbles. Bright luminescence along the edges of fractures, quartz cements and quartz overgrowths in dolomite marbles, low δD values of micas, negative δ13C values and low δ18O values of calcite and dolomite, and depleted δ18O values of quartz from dolomite marbles all indicate that meteoric fluids interacted with Lone Mountain marbles during the Tertiary. Partial oxygen isotopic exchange between calcite and low 18O meteoric fluids lowered the δ18O values of calcite, resulting in uniform quartz-calcite fractionations that define an apparent pseudoisotherm. These quartz-calcite fractionations significantly underestimate both the temperature of metamorphism and the temperature of post-metamorphic alteration. Partial oxygen isotopic exchange between quartz and meteoric fluids also resulted in 18O depletion of quartz from dolomite marbles. This partial exchange was facilitated by an increase in the surface area of the quartz as a result of its dissolution by meteoric fluids. The negative δ13C values in carbonates result from the oxidation of organic material by meteoric fluids following metamorphism. Stable isotopic data from Lone Mountain marbles are consistent with the extensive circulation of meteoric hydrothermal fluids throughout western Nevada in Tertiary time. Received: 1 February 1994/Accepted: 12 September 1995  相似文献   

5.
The whole-rock δ 18O values of samples from twelve discrete Archean plutons intruding the western Wabigoon granite-greenstone belt, northwestern Ontario, range from 6.8 to 9.5‰. Most samples with δ 18O > 8.7‰, however, come from portions of the Burditt Lake stock, or the Esox Lake area, that have been affected by deuteric or metasomatic activity. The distribution of δ 18O values for the remaining samples is very similar to that known for the large batholithic complexes and gneissic terrains that dominate this portion of northwestern Ontario. The generally low δ 18O values of the discrete granitoid plutons suggest that 18O-rich supracrustal rocks were unimportant in their genesis. Like the granitoids of the batholithic complexes and gneissic terrains, the discrete granitoid plutons represent new additions to the Archean sialic crust.  相似文献   

6.
Gypsum and celestine crystals coexisting with those of calcite and dolomite in marble geodes from the Apuan Alps (Italy) display oxygen-isotopic ratios of between +25.8 and +27.8‰ relative to SMOW, with an average value of +27.2‰.The δ 18O and δ 13C values of calcite-dolomite-marble assemblages fall in the range of marine limestone, the dolomites being enriched by about 1‰ both for oxygen and carbon isotopes.The homogeneity of gypsum and celestine δ 18O values seems to reflect an isotopic equilibrium of sulfate ions with environmental water, prior to their precipitation and at a temperature higher than 40°C.The calcite-dolomite pairs are not in isotopic equilibrium, and their oxygen-isotopic fractionations cannot be used as indicators of their deposition temperatures.  相似文献   

7.
This study couples in situ 16O, 17O and 18O isotope and in situ trace element analyses to investigate and characterize the geochemical and textural complexity of magmatic-hydrothermal quartz crystals. Euhedral quartz crystals contemporaneous with mineralization were obtained from four magmatic-hydrothermal ore deposits: El Indio Au–Ag–Cu deposit; Summitville Au–Ag–Cu deposit; North Parkes Cu–Au deposit and Kingsgate quartz-Mo–Bi–W deposit. The internal features of the crystals were imaged using cathodoluminescence and qualitative electron microprobe maps. Quantitative isotopic data were collected in situ using 157 nm laser ablation inductively coupled plasma mass spectrometry (for 40 trace elements in quartz) and sensitive high-resolution ion microprobe (for 3 isotopes in quartz). Imaging revealed fine oscillatory zoning, sector zoning, complex “macromosaic” textures and hidden xenocrystic cores. In situ oxygen isotope analyses revealed a δ18O range of up to 12.4 ± 0.3 ‰ in a single crystal—the largest isotopic range ever ascribed to oscillatory zonation in quartz. Some of these crystals contain a heavier δ18O signature than expected by existing models. While sector-zoned crystals exhibited strong trace element variations between faces, no evidence for anisotropic isotope fractionation was found. We found: (1) isotopic heterogeneity in hydrothermal quartz crystals is common and precludes provenance analysis (e.g., δD–δ18O) using bulk analytical techniques, (2) the trace element signature of quartz is not an effective pathfinder toward noble metal mineralization and (3) in three of the four samples, both textural and isotopic data indicate non-equilibrium deposition of quartz.  相似文献   

8.
The unidirectional solidification textures (UST) quartz is generally thought to form from fluids exsolved from shallow intrusions and/or magma chambers, but such an idea is still poorly constrained from the evidence of stable isotopes. In this study, we report for the first time the δ18O of quartz that shows UST from the Qulong Cu–Mo and the Yechangping Mo porphyry deposits in China. The analysis results show that the UST quartz samples from the Qulong deposit have δ18O values ranging from +6.2 ‰ to +7.6 ‰, which are similar to that of quartz phenocrysts (+6.7 ‰ to +7.8 ‰). In contrast, the UST quartz samples from the Yechangping porphyry Mo deposit yield a high δ18O value (+10.0 ‰). The δ18Owater value of Yechangping UST quartz (+8.5 ‰) is also higher than that of Qulong (+4.6 ‰ to +5.8 ‰). Hydrothermal biotite from potassic alteration and sericite from early phyllic alteration at Qulong have similar δ18O values to UST quartz, suggesting the involvement of magmatic fluids during this stage of deposit evolution.  相似文献   

9.
Oxygen isotope microanalyses of authigenic quartz, in combination with temperatures of quartz precipitation constrained by fluid inclusion microthermometry and burial history modelling, are employed to trace the origin and evolution of pore waters in three distinct reservoirs of the Brae Formation in the Miller and Kingfisher Fields (North Sea). Oxygen isotope ratios of quartz cements were measured in situ in nine sandstone thin sections with a Cameca ims-4f ion microprobe. In conjunction with quartz cement paragenesis in the reservoirs, constrained from textural and cathodoluminescence (CL) microscopy studies, pore water evolution was reconstructed from the time of deposition of the sandstones in the Upper Jurassic until the present.CL photomicrographs of quartz overgrowths in the Brae Formation sandstones show three cement zones (A, B and C) which can be related to different oxygen isotope compositions: (1) the earliest, and thinnest, zone A (homogeneous CL pattern with probable δ18O values between +23‰ and +26‰—direct measurements were not possible) precipitated in the sandstones at temperatures <60 °C; (2) the second zone B (complex CL pattern and directly measured δ18O values between +15‰ and +18‰) precipitated in the sandstones most likely between 70 and 90 °C; (3) the third zone C (homogeneous CL pattern and directly measured δ18O values between +16‰ and +22‰) precipitated in the sandstones most likely at temperatures >90 °C. Calculated oxygen isotope compositions of pore waters show that zone A quartz cements, and enclosing concretionary calcite, precipitated from a meteoric-type fluid (∼−7‰) during shallow burial (<1.5 km). Zone B quartz cements precipitated from fluids which evolved in composition from a meteoric-type fluid (δ18O −7‰) to a more 18O-enriched fluid (δ18O −4‰) as burial continued to ∼3.0 km. Data from zone C quartz cements are consistent with further fluid evolution from δ18O −4‰ to basinal-type fluids with δ18O similar to the present-day formation water oxygen isotope composition (+0.6‰ at 4.0 km burial). A similar pore water evolution can be derived for all three reservoirs studied, indicating that hydrogeologic evolution was similar across sandstones of the whole Brae Formation.The quartz cement zones observed in the Brae Formation sandstones, and the pore water history derived for the area studied, is analogous to published petrographic and pore water evolution data from the nearby Brent Group reservoirs and from reservoirs located in the Haltenbanken area on the Atlantic margin offshore Norway. Considering quartz cement is a major porosity-occluding phase in many reservoir sandstones, and because pore waters both dissolve quartz and carry the dissolved silica to cementation sites, the data presented are valuable for improving the understanding and prediction of reservoir quality development in sandstones globally.  相似文献   

10.
In the Strangways Range a broad tract of lower Proterozoic mafic and silicic granulites with δ 18O = 0.1 to 7.3% is depleted in 18O on average by 2–47% compared with high-grade gneisses and granitoids of Canada and other shields. The Fraser Range mafic granulites (δ18O ~ 7.2%) are enriched with respect to unaltered sea-floor basalts (~5.7%).In some rocks depletion in 18O could be related to dehydration during granulite-facies metamorphism and removal of the resultant products of partial melting. In other rocks pre-granulite reaction between heated seawater and hot basic intrusives seems to be a plausible mechanism of depletion in 18O. A direct correlation between depletion in 18O and the abundance of brown granulite hornblende suggests that 18O-depleted water was present in certain mafic rocks before the onset of granulite metamorphism, whereas in others brown hornblende was introduced during a phase of the granulite facies metamorphism itself.  相似文献   

11.
Fine quartz silt (1–10μm dia, important in aerosol dust) isolated from a large number of soils, as well as Phanerozoic shales, sandstones and recent sands of the southern African stratigraphie column (Carboniferous, Permian and Triassic) exhibits a mean δ18O of 12.2 ± 2.1%0. These values are similar to those reported for South Pacific pelagic sediments and adjacent land areas of similar latitude but are lower than those reported for this size fraction of 30 Mesozoic and Paleozoic shales (20.7 ± 1.8%.) and soils from mid-continental U.S.A., for aerosol quartz in the North Pacific pelagic sediments, and for eolian caps in high-elevation soils of Hawaii. The lower oxygen isotopic ratios in fine quartz silt of southern Africa reinforces the earlier indication that Southern Hemisphere detritai sedimentary reservoirs contain a higher proportion of igneous and metamorphic quartz (lower δ18O) and less lowtemperature authigenic quartz (higherδ18O) than Northern Hemisphere detritai sediments. The difference reflects climates, as continents drifted in latitude.  相似文献   

12.
The relationships between the δ18O of quartz veins and veinlets pertaining to the main stage of gold mineralization at the Sukhoi Log deposit and metasomatically altered host slates are estimated. The oxygen isotopic composition of veined quartz and host slates is not uniform. The δ18O of quartz veins from the Western, Central, and Sukhoi Log areas of the deposit vary from +16 to + 18 ‰. The δ18O range of metasomatically altered slates in the Western and Sukhoi Log areas attains 6 ‰. The δ18O of quartz veins are always higher than those of host slates by 3–7‰. The regular difference in the δ18O between quartz veins and host slates indicates that the oxygen isotopic composition of the ore-bearing fluid forming the system of quartz veins and veinlets at the Sukhoi Log deposit could have formed as a result of interaction with silicate rocks, for instance, terrigenous slates enriched in δ18O. Such interaction, however, took place at deeper levels of the Sukhoi Log deposit. It is suggested that the fluid phase participating in the formation of the vein and veinlet system had initially high δ18O(>+10‰) due to interaction with the rocks enriched in δ18O at a low fluid/rock ratio. The oxygen isotope data indicate that the fluid participating in the formation of gold mineralization at the Sukhoi Log deposit was not in equilibrium with igneous rocks at high temperatures.  相似文献   

13.
The extent of quartz cementation in shallow marine sandstones of the Brora Arenaceous Formation (Oxfordian) is closely related to the occurrence and abundance of Rhaxella perforata sponge spicules. Three cement morphologies are identified, chalcedonic quartz, microquartz and mesoquartz. Chalcedonic quartz forms matrix-supported cements which preserve moulds of Rhaxella spicules. Chalcedonic quartz crystals have inequant development of crystal faces, on average 0·1 μm in diameter, and are the first formed cement and reveal homogeneous dark grey tones on the SEM-CL/BEI. Microquartz forms 5–10 μm diameter crystals, which commonly grow on chalcedonic quartz substrates and show various grey tones under SEM-CL/BEI. Mesoquartz crystals grow in optical continuity with their host grains, have >20 μm a-axial diameter crystals, and exhibit distinctly zoned luminescence. Although no opaline silica is preserved, the quartz cement is interpreted to have formed from an opaline precursor. Detrital quartz has an average δ18O composition of + 12·2‰ and mesoquartz (syntaxial overgrowth) has an average δ18O composition of +20·0‰. Estimates of the δ18O compositions of microquartz and chalcedonic quartz are complicated by the problem of isolating the two textural types; mixtures of the two give consistently higher δ18O compositions than mesoquartz, the higher estimate being +39·2‰. From oxygen isotope data the formation of quartz, microquartz and chalcedonic quartz is interpreted to have taken place between 35 and 71°C in marine derived pore waters. Organic and inorganic maturation data constrain the upper temperature limit to less than 60°C.  相似文献   

14.
Nodular chert from the middle and upper Arbuckle Group (Early Ordovician) in the Slick Hills, SW Oklahoma, was formed by selective replacement of grainstones, burrow fillings, algal structures, and evaporite nodules. Chert nodules are dominantly microquartz with minor fibrous quartz (both quartzine and chalcedony), megaquartz, and microflamboyant quartz. Lepisphere textures of an opal-CT precursor are preserved in many (especially in finely-crystalline) chert nodules. The δ18O values of microquartz chert range from +23.4 to + 28.80/00 (SMOW), significantly lower than those of Cenozoic and Mesozoic microquartz chert formed both in the deep sea and from near-surface sea water. The δ18O values of chert decrease with increasing quartz crystal size. Silicification in the Arbuckle Group occurred during early diagenesis, with the timing constrained by the relative temporal relationships among silicification, burial compaction, and early dolomite stabilization. Silica for initial chert nucleation may have been derived from both dissolution of sponge spicules and silica-enriched sea water. Chert nucleation appears to have been controlled by the porosity, permeability, and organic matter content of precursor sediments. This conclusion is based on the fact that chert selectively replaced both porous grainstones and burrows and algal structures enriched in organic matter. Growth of chert probably occurred by a maturation process from opal-A(?), to opal-CT, to quartz, as indicated by the presence of opal-CT precursor textures in many chert nodules. Although field and petrographic evidence argues for an early marine origin for chert in the Arbuckle Group, the light δ18O values are inconsistent with this origin. Meteoric resetting of the δ18O values of the chert during exposure of the carbonate platform best explains the light δ18O values because: (i) the δ18O values of chert nodules decrease with decreasing δ18O values of host limestones, and (ii) chert nodules from early dolomite, which underwent more extensive meteoric modification than associated limestones, have lighter δ18O values than chert nodules from limestones. Increasing recrystallization of chert nodules by meteoric water resulted in progressive 18O depletion and (quartz) crystal enlargement.  相似文献   

15.
Oxygen isotope compositions were measured by ion microprobe in individual micrometer-sized quartz grains extracted from one aerosol sample collected on the Cape Verde Islands and from four surface samples (three soils and one sediment) representing potential source regions of aerosols in Western and Central Africa (Morocco, Algeria, Niger, and Chad). A large range of δ18O values, from +6.2‰ to +39.3‰ is present within the aerosol quartz grains. The different size fractions of the quartz grains from the surface samples overlap nearly entirely this range but show significant differences in their δ18O distributions for the different size fractions of the grains (i.e., different modes, different proportions of grains with low or high δ18O, ...). These differences in δ18O distributions can be related to different geological formations (i.e., mantle-derived magmatic rocks, crustal magmatic rocks, or sedimentary rocks) outcropping in each region, thus giving a fingerprint of the source region. Quartz grains with unusually high δ18O values between +30‰ and +40‰ were attributed to lacustrine cherts formed in evaporitic environments (Chad basin).The existence of distinct δ18O distributions for the surface samples, which reflect regional geology but indicate some transport of the grains, enables the characterization of mixing processes during dust emission in the atmosphere. Particles are mixed at a regional scale in the dust reservoir, but injection of fine particles into the high troposphere occurs as a discrete and localized event with no mixing during the subsequent long-range transport by the easterlies. The comparison of the δ18O distribution of the quartz from the aerosol sample with the equivalent size fractions in surface samples shows that the Niger area is the more probable source region for the aerosol although the Moroccan source cannot be excluded. This method gives a valuable tool to trace the source region of dust into the atmosphere or into sediment samples, allowing the reconstruction of air mass circulations.  相似文献   

16.
Abstract Coexisting quartz, feldspar and biotite vary widely in their δ18O values and display a remarkable 18O / 16O disequilibrium relation; especially, a quartz–feldspar reversal (Δ 18OQuartz?feldspar<0) exsists in the Aral granite pluton of the Altay Mountains, northern Xinjiang. The 18O / 16O exchange reaction definitely occurred between granite and water. Initial δ18O values of the granite and exotic fluid are evaluated by the mass balance consideration. The conventional method of discrimination between various magma derivations simply with δ18O values of either whole rock or separate minerals is misleading and unreliable. Experiments carried out by the authors show that the 18O / 16O exchange reaction is not accompanied by what geologists describe as petrological and mineralogical alteration effect. This decoupling relation implies that exchange reaction occurs at a relatively high temperature during subsolidus–postmagmatic cooling of magmas. The exchange mechanism is mainly diffusion–controlled. It is demonstrated through quantitative modelling that the hydrothermal system associated with the Aral pluton is long–lived (0.8—6 Ma), with a relatively high fluid flow rate (3 x 10?14 mol. s?1) and high W/ R ratio (0.79-6.14). This means that an intense flow and convection may exist at the midcrustal level of orogenic magmatic arcs.  相似文献   

17.
Variations in the oxygen isotope composition (δ18O) of five cherts from the 1.9 Ga Gunflint iron formation (Canada) were studied at the micrometer scale by ion microprobe to try to better understand the processes that control δ18O values in cherts and to improve seawater paleotemperature reconstructions. Gunflint cherts show clearly different δ18O values for different types of silica with for instance a difference of ≈15‰ between detrital quartz and microquartz. Microquartz in the five samples is characterized by large intra sample variations in δ18O values, (δ18O of quartz varies from 4.6‰ to 6.6‰ at the 20 μm scale and from ≈12‰ to 14‰ at 2 μm scale). Isotopic profiles in microquartz adjacent to hydrothermal quartz veins demonstrate that microquartz more than ≈200 μm away from the veins has preserved its original δ18O value.At the micrometer spatial resolution of the ion probe, data reveal that microquartz has preserved a considerable δ18O heterogeneity that must be regarded as a signature inherited from its diagenetic history. Modelling of the δ18O variations produced during the diagenetic transformation of sedimentary amorphous silica precursors into microquartz allows us to calculate seawater temperature (Tsw at which the amorphous silica precipitated) and diagenesis temperature (Tdiagenesis at which microquartz formed) that reproduce the δ18O distributions (mean, range and shape) measured at micrometer scale in microquartz. The two critical parameters in this modelling are the δ18O value and the mass fraction of the diagenetic fluid. Under these assumptions, the most likely ranges for Tsw and Tdiagenesis are from 37 to 52 °C and from 130 to 170 °C, respectively.  相似文献   

18.
18O/16O ratios have been obtained for 134 whole-rocks and minerals from metamorphic and granitic rocks of the Yanai district in the Ryoke belt, Southwest Japan. The 18O/16O ratios of pelitic rocks of the marginal metamorphic zone decrease progressively with increasing metamorphic grade. In the gneiss-granite complex (zone of migmatite [1]), the most characteristic feature of the rocks is that oxygen isotopic homogenization proceeds on both local and regional scales in parallel with “granitization” or chemical homogenization. Granitic rocks of various origin are fairly uniform in isotopic composition with δ 18O of quartz of 12 to 14‰ (SMOW) and δ 18O of biotite of 7 to 9‰ and are about 3 to 4‰ enriched in 18O compared to other Cretaceous granites of non-metamorphic terranes in Japan. The high 18O/16O ratios of granitic rocks of this district were discussed in relation to the 18O-depletion in metasediments. Oxygen isotopic fractionations among coexisting minerals from various rock-types of the gneiss-granite complex indicate that these minerals were formed under near isotopic equilibrium at a temperature of about 600 to 700° C. Some abnormal fractionations of quartz-biotite pairs also were obtained for rocks which had undergone a progressive 18O-depletion or 18O-enrichment. This is due to high resistivity of quartz and contrastive susceptibility of biotite to isotopic exchange during metamorphism and “granitization”.  相似文献   

19.
 Previous stable isotope studies at Lizzies Basin revealed that metasedimentary rocks are 18O-depleted relative to protolith values, particularly in the lower parts of the section (Lower Zone) where the rocks are also isotopically homogeneous on a scale of hundreds of meters (quartz δ18O=+9.0 to +9.6 per mil). In contrast, metasedimentary rocks at higher levels at Lizzies Basin (Upper Zone) are less 18O-depleted and more heterogeneous in δ18O. In order to understand more fully the isotopic evolution of this terrane, a series of detailed, meter-scale traverses across various metamorphic and igneous lithologies were completed at Lizzies Basin, and at the structurally higher Angel Lake locality. Traverses in the Lizzies Basin Lower Zone and in the lower parts of Angel Lake (Angel Lake Lower Sequence) across various silicate lithologies, including abundant granitoids, reveal similar degrees of homogeneity, although the average δ18O values are higher at Angel Lake. In contrast, traverses which include substantial thicknesses of marble and calc-silicate gneiss and very little granitoid have more heterogeneous quartz δ18O values (+11.9 to +13.4 per mil), and also have a higher average δ18O (+12.9 per mil), than observed elsewhere. The scale of 18O/16O homogeneity in quartz observed at Lizzies Basin and Angel Lake (meters to hundreds of meters) requires fluid-mediated isotope exchange, which accompanied Tertiary metamorphism. There is a correlation between the degree of 18O-depletion in metasedimentary rocks, 18O/16O homogenization between lithologies, and the proportion of granitoids (leucogranites in particular) within any part of the section, and a corresponding anticorrelation with the proportion of marble. This points to a causal relationship, whereby the leucogranites (as well as the Tertiary hornblende diorite and biotite monzogranite) acted as both a relatively low-18O reservoir and a source of fluids to enhance exchange, while the marbles hindered isotope depletion and homogenization by acting as relatively high-18O reservoirs and impermeable layers. Material balance calculations help delineate the plausible mechanisms of exchange between granitoids and metasediments. Single-pass infiltration of magmatic fluids from the granitoids is not capable of reproducing all of the observations. Fluid-mediated exchange by convective recirculation of magmatic fluids on a scale of meters is the mechanism which explains all of the observations. The generalized model for the isotopic evolution of the East Humboldt Range core complex provides an excellent opportunity to establish the main causes and controlling factors of 18O-depletion and 18O/16O homogenization during regional metamorphism. Received: 27 July 1993 / Accepted: 1 July 1994  相似文献   

20.
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