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1.
Magnesite forms a series of 1‐ to 15‐m‐thick beds within the ≈2·0 Ga (Palaeoproterozoic) Tulomozerskaya Formation, NW Fennoscandian Shield, Russia. Drillcore material together with natural exposures reveal that the 680‐m‐thick formation is composed of a stromatolite–dolomite–‘red bed’ sequence formed in a complex combination of shallow‐marine and non‐marine, evaporitic environments. Dolomite‐collapse breccia, stromatolitic and micritic dolostones and sparry allochemical dolostones are the principal rocks hosting the magnesite beds. All dolomite lithologies are marked by δ13C values from +7·1‰ to +11·6‰ (V‐PDB) and δ18O ranging from 17·4‰ to 26·3‰ (V‐SMOW). Magnesite occurs in different forms: finely laminated micritic; stromatolitic magnesite; and structureless micritic, crystalline and coarsely crystalline magnesite. All varieties exhibit anomalously high δ13C values ranging from +9·0‰ to +11·6‰ and δ18O values of 20·0–25·7‰. Laminated and structureless micritic magnesite forms as a secondary phase replacing dolomite during early diagenesis, and replaced dolomite before the major phase of burial. Crystalline and coarsely crystalline magnesite replacing micritic magnesite formed late in the diagenetic/metamorphic history. Magnesite apparently precipitated from sea water‐derived brine, diluted by meteoric fluids. Magnesitization was accomplished under evaporitic conditions (sabkha to playa lake environment) proposed to be similar to the Coorong or Lake Walyungup coastal playa magnesite. Magnesite and host dolostones formed in evaporative and partly restricted environments; consequently, extremely high δ13C values reflect a combined contribution from both global and local carbon reservoirs. A 13C‐rich global carbon reservoir (δ13C at around +5‰) is related to the perturbation of the carbon cycle at 2·0 Ga, whereas the local enhancement in 13C (up to +12‰) is associated with evaporative and restricted environments with high bioproductivity.  相似文献   

2.
The Dafulou and Huile vein and stratabound cassiterite-sulfide deposits and sheeted ore veins at the Kangma cassiterite-sulfide deposit are located in the eastern part of the Dachang tin field. These deposits are hosted in a sedimentary sequence containing significant concentrations of organic matter in the form of Lower Devonian calcareous black shales and hornfels. These rocks together with the younger intrusion of Longxianggai granite (91DŽ Ma) actively participated in the formation of Sn-polymetallic deposits. The following three major stages have been distinguished in stratiform and vein-type orebodies at Dafulou, Huile and Kangma: stage I (cassiterite, pyrrhotite, arsenopyrite, tourmaline, carbonate), stage II - main sulfide stage (quartz, cassiterite, arsenopyrite, pyrrhotite, sphalerite, stannite, pyrite, carbonates) and stage III (native Bi, galena, electrum, sulfosalts). Stage IV (post-ore), recognized at Huile is represented by barren carbonates and zeolites. Whole rock geochemistry has revealed that at Dafulou, Bi and Cu correlate strongly with S, whereas V and Pb correlate well with Corg (organic carbon). The similar distribution patterns of selected elements in average slightly mineralized low-Ca black shales indicate a fluid composition similar for all deposits studied. Studies of graphitization of the organic matter in black shales adjacent to orebodies indicate that d(002) and FWHM (full width in half maximum)/peak height values gradually decrease in the following sequence: Dafulou deposit M Kangma deposit M Huile deposit. The pyrolysate of wall rocks at the Dafulou deposit is relatively enriched in asphaltenes and maltenes (55.6-72.0% of the pyrolysate) comparable with pyrolysate obtained from more distal black shales (19.2-28.5%). Typical GC-MS spectra of pyrolysate from distal black shales are dominated by alkanes in the n-C15 to n-C25 range, aromatic molecules being represented mostly by alkyl-naphthalenes. In contrast, only traces of aliphatic hydrocarbons in the n-C14 to n-C18 range and elemental sulfur were identified in pyrolysates from pyrrhotitized wall rocks. The earliest fluid inclusions of the studied system occur in the quartz-tourmaline-cassiterite assemblage of stage I at Dafulou. These inclusions are H2O-CO2-CH4-rich, with 10 to 20 vol% of aqueous phase. P-T conditions of the trapping of inclusions are estimated to be up to 400 °C and 1.3 to 2.0 kbar (between 5.0 and 7.5 km under lithostatic pressure). In contrast, the presence of a low density gaseous CO2-CH4 phase indicates relatively low pressures during the formation of the breccia-type quartz-calcite-cassiterite-sulfide mineralization (stage II), when P-T conditions probably reached approx. 380 to 400 °C and 0.6 kbar (up to 6 km under hydrostatic pressure). Fluid inclusion data and oxygen isotope thermometry indicate that cassiterite-sulfide ores of the main sulfide stage (stage II) formed from aqueous-carbonic fluid (CO2/CH4 =ᄺ) at temperatures of up to 390 °C at Dafulou and in a temperature range of 250 to 360 °C at Huile and 260 to 370 °C at Kangma. The '34S values of sulfides from Dafulou range mostly between -1 and -6‰, whereas sulfides from the Kangma and Huile deposits are characterized by more negative '34S values (between -8 and -11‰, and between -9 and -12‰, respectively). These data suggest that bacteriogenic sulfides of black shales were a dominant source of reduced sulfur for epigenetic (vein and replacement) mineralization. Oxygen isotopic compositions of five quartz-cassiterite pairs from Dafulou and Huile show a relatively narrow range of calculated oxygen isotope temperatures (250-320 °C, using the equation of Alderton 1989) and high '18Ofluid values between +8 and +10‰ (SMOW), which are in agreement with fluid derivation from and/or high temperature equilibration with the Longxianggai granite. The carbon and oxygen isotope composition of carbonates reflects variable carbon sources. Stage I calcite is characterized by narrow ranges of '13C (-7.0 to -9.5‰ PDB) and '18O (+15.0 to +17.5‰ SMOW). This calcite shows ubiquitous deformation, evidenced by intense development of twins. Fluid compositions calculated at 330 °C for the Dafulou and Huile deposits and at 270-300 °C for the Kangma deposit ('18Ofluid between +10.0 and +11.5‰ SMOW, '13Cfluid between -5.5 and -7.5‰ PDB), agree with fluid derivation from and/or equilibration with the peraluminous, high-'18O Longxianggai granite and suggest a significant influence of contact metasedimentary sequences (carbon derived from decomposition and/or alteration of organic matter of calcareous black shales). The '13 C values of organic matter from the Lower to Upper Devonian host rocks at the Dafulou deposit (-24.0 and -28.0‰) fit with a marine origin from algae. However, organic matter adjacent to the host rock-ore contact displays a slight enrichment in 13C. The organic carbon from the Huile and Kangma deposits is even more 13C enriched (-24.6 to -23.5‰). The most heavy '13 C values (-16.5‰) were detected in hornfels sampled at the contact of the Upper Devonian sediments with the Longxianggai granite. The '13C data broadly correlate with the degree of structural ordering (degree of graphitization) of organic matter, which indicates that both variables are related to thermal overprint.  相似文献   

3.
Several types of anhydrite-bearing rocks have been found in the amphibolite-facies metamorphosed rocks at the north-eastern margin of the Moldanubian Zone. Anhydrite either forms monomineralic bands up to 40 cm thick, or occurs in the form of disseminated grains in surrounding calc-silicate gneiss together with feldspar, scapolite, amphibole, pyroxene, epidote and pyrite. The isotopic composition of sulphur ('34S=30.6 to 32.3‰) and strontium (87Sr/86Sr=0.70797 to 0.70781) in anhydrite may indicate a marine source of sulphate. The isotopic ratio of strontium is in the same range as that of metamorphosed strata-bound barite-sulphide ores, which have been previously described in the same area. The '34S values of coexisting pyrite range from 21.4 to 22.5‰, the (34Sanhydrite-pyrite corresponding to the metamorphic temperature of 600 to 660 °C. In contrast to many submarine-exhalative deposits, the oxygen isotopic compositions of anhydrite ('18O=9.3 to 10.2‰) are lighter than that of barite ('18O=10.4 to 13.8‰). This indicates that the both minerals are not in isotopic equilibrium. Therefore, it is probable that anhydrite and barite from the Ro—ná district were deposited from fluids that contained different proportions of seawater and hydrothermal fluids or from hydrothermal fluids that underwent variable extent of oxygen isotope exchange with seafloor rocks. The '13C values in calcite ('13C=-17.2 to -18.7‰) from anhydrite-bearing rock are lower than those in distant marbles. As graphite is absent in anhydrite- and calcite-bearing rocks, impoverishment in the 13C isotope cannot be attributed to the graphite-carbonate isotopic exchange during metamorphism. It is proposed that low '13C values in carbonates are caused by pre-metamorphic oxidation of organic matter in course of hydrothermal processes. Anhydrite and anhydrite-bearing calc-silicate gneiss from the north-eastern part of the Moldanubian Zone are interpreted to be the high-grade metamorphosed analogue of anhydrite-rich exhalites commonly found in submarine-exhalative hydrothermal deposits.  相似文献   

4.
Anomalous geogenic arsenic occurs in drinking water from the Goose River crystalline ground-watershed in mid-coastal Maine. Isotope investigations were useful in understanding release areas of arsenic into affected water wells. The isotope composition of sulfate associated with probable arsenian pyrite oxidation is described. Correlation of '18OSO4 enrichment [+4.57 to +7.46‰ Vienna Standard Mean Ocean Water (VSMOW)] is discussed with specific and recurring areas of elevated arsenic (10-52 µg l-1). Although arsenic concentrations were highly variable over 2 years per well, '18OSO4 values were always consistent and suggested a specific and consistent risk for elevated arsenic occurrences for each well. The '18O values in the water molecule (-12.07 to -8.81‰ VSMOW) and the '18OSO4 values may serve as prospective indicators of prominent zones of aeration at depth in discrete fracture zones. The '18O values in the water molecule and sulfate ion appear to indicate that more than 60% of O2 incorporated into the SO42- ion are from dissolved oxygen and belong to distinct fractured areas. These aeration zones or oxidation fronts, as outlined by oxygen isotopes, are sentinels for high arsenic risk in groundwater.  相似文献   

5.
A large number of Variscan mesothermal gold deposits are located in the central part of the Bohemian Massif, close to the Central Bohemian Plutonic Complex. The Petrá)kova hora deposit has many features that distinguish it from other deposits in the region and suggest its mineralization is closely related to the late magmatic processes associated with the Petrá)kova hora granodiorite. The gold ores occur as sheeted arrays of quartz veins and veinlets hosted by the small Petrá)kova hora granodiorite stock. Gold is found mainly as free grains of >900 fineness, and is accompanied by abundant pyrrhotite and chalcopyrite, and accessory pyrite, arsenopyrite, loellingite, and molybdenite. Molybdenite from the Petrá)kova hora deposit has been dated by the Re-Os method at 344.4DŽ.8 Ma. Hydrothermal alteration in the Petrá)kova hora deposit exhibits a distinct temporal paragenesis. Selectively pervasive, early K-alteration and silicification are the oldest hydrothermal phases. These were followed by early quartz veins (Q1 to Q4) that contain most of the gold mineralization. Late quartz veins (Q5) and fracture-controlled silicification are gold-poor or barren. Barren calcite veins are the youngest hydrothermal product. Extensive low-temperature, meteoric-water dominated alteration, as is typical of classic porphyry deposits, is absent. However, the lower '18O whole rock values for Petrá)kova hora granodiorite and aplite (+2.4 to +5.1‰ SMOW) compared to other intrusions in the region reflect either interaction with isotopically light external fluids or magma assimilation of small volumes of hydrothermally altered country rock. The '18O isotopic compositions for quartz, scheelite and hornblende (7.7 to 13.4‰ SMOW) and the '34S compositions for sulfide minerals (-1 to +3.5‰ CDT) from early, gold-rich quartz veins indicate formation at high temperatures (590 to 400 °C) from fluids with a magmatic isotopic signature ('18OFLUID of 5.7 to 7.2‰). Fluids related to late quartz veins (Q5) suggest the presence of a significant component of non-magmatic water ('18OFLUID: +2.5 to +4.0‰). The '34S values of post-Q5 sulfide minerals (-4.5 to -3.5‰) reflect at least partial derivation of late-stage sulfur from a source external to the intrusions. Aqueous, aqueous-carbonic and nitrogen-bearing fluid inclusions were identified in hydrothermal and igneous quartz, with the aqueous inclusions being the most common. In hydrothermal vein quartz, the salinity of primary aqueous inclusions falls into ranges 6 to 23 and 33 to 41 equiv. wt% NaCl; in igneous quartz, populations in salinity were observed between 5 to 16, 35 to 40 and 62 to 70 equiv. wt% NaCl. The salt component of these fluids is best, and minimally, approximated by the NaCl-KCl-CaCl2 system. Low- and high-salinity aqueous-carbonic inclusions are accessory in many of the analyzed samples. Three large successive pulses of fluids are recognized. Each pulse begins with a high-salinity (>30 equiv. wt% NaCl) magmatic fluid and evolves toward a lower salinity (~5 equiv. wt% NaCl) fluid. Data suggest that external (meteoric?) water(s) were significant for only the third fluid pulse, which formed the late Q5 quartz veins and the calcite veins. Polyphase fluid inclusions hosted by igneous quartz of the Petrá)kova hora granodiorite indicate minimum trapping conditions of about 3 kbar and 550 °C. The gold-rich Q1 to Q4 veins may have formed along a quasi-isobaric cooling path at 2.5 to 1.5 kbar and 590 to 400 °C. This was followed by uplift, and formation of late Q5 quartz veins (0.5 to 1.5 kbar; ~300 °C) and post-ore calcite veins (<0.5 kbar; 100 to 140 °C). The characteristics of the Petrá)kova hora deposit suggest that it may represent a position intermediate between intrusion-related gold systems (e.g., Fort Knox deposit, Alaska) and gold-rich, copper-poor porphyry deposits (e.g., Maricunga Belt in Chile). As such, the Petrá)kova hora deposit might be an example of the reduced gold sub-type of porphyry deposit.  相似文献   

6.
The Mallery Lake area contains pristine examples of ancient precious metal-bearing low-sulfidation epithermal deposits. The deposits are hosted by rhyolitic flows of the Early Proterozoic Pitz Formation, but are themselves apparently of Middle Proterozoic age. Gold mineralization occurs in stockwork quartz veins that cut the rhyolites, and highest gold grades (up to 24 g/t over 30 cm) occur in the Chalcedonic Stockwork Zone. Quartz veining occurs in two main types: barren A veins, characterized by fine- to coarse-grained comb quartz, with fluorite, calcite, and/or adularia; and mineralized B veins, characterized by banded chalcedonic silica and fine-grained quartz, locally intergrown with fine-grained gold or electrum. A third type of quartz vein (C), which crosscuts B veins at one locality, is characterized by microcrystalline quartz intergrown with fine-grained hematite and rare electrum. Fluid inclusions in the veins occur in two distinct assemblages. Assemblage 1 inclusions represent a moderate temperature (Th=150 to 220 °C), low salinity (~1 eq. wt% NaCl, with trace CO2), locally boiling fluid; this fluid type is found in both A and B veins and is thought to have been responsible for Au-Ag transport and deposition. Assemblage 2 inclusions represent a lower temperature (Th=90 to 150 °C), high salinity calcic brine (23 to 31 wt% CaCl2-NaCl), which occurs as primary inclusions only in the barren A veins. Assemblage 1 and 2 inclusions occur in alternating quartz growth bands in the A-type veins, where they appear to represent alternating fluxes of dilute fluid and local saline groundwater. No workable primary fluid inclusions were observed in the C veins. The A-vein quartz yields '18O values from 8.3 to 14.5‰ (average=10.9ǃ.7‰ [1C], n=30), whereas '18O values for B-vein quartz range from 11.2 to 14.0‰ (average=13.0ǂ.9‰, n=12). Calculated '18OH2O values for the dilute mineralizing fluid from B veins range from -2.6 to 0.2‰ (average=-0.8ǂ.9‰, n=12) and are consistent with a dominantly meteoric origin. No values could be calculated for the brine, however, because all A-vein quartz samples contain mixed fluid inclusion populations. However, the fact that A-vein quartz samples extend to lower '18O values than the B veins suggests that the brine had a lighter isotopic signature relative to the dilute fluid. Hydrogen isotopic ratios of fluid inclusion waters extracted from eleven quartz samples of both vein types range from 'DFI=-56 to -134‰, but show no particular correlation with vein type. In most respects, the mineralogical and fluid characteristics of the Mallery Lake system are comparable to those of Phanerozoic low-sulfidation deposits, and although the presence of high salinity brines is unusual in such deposits, it is not unknown (e.g., Creede, Colorado). In addition, one of the few other examples of well-preserved, Precambrian, low-sulfidation epithermal deposits, from the Central Pilbara tectonic zone, Australia, contains a similarly bimodal fluid assemblage. The significance of these saline brines is not clear, but from this study we infer that they were not directly involved with Au-Ag transport or deposition.  相似文献   

7.
The 750-Ma Seychelles granites have whole-rock '18O values that range from -1.2 to +7.5‰. Differences in '18O values between quartz, feldspar and whole-rock for samples that have a range of '18O values suggest that these minerals are in magmatic equilibrium, and that the whole-rock '18O values were little affected by post-crystallization interaction with fluids. Two suites of granites (the Mahé type and the Praslin type) have previously been recognized on the basis of chemical and radiogenic isotope composition. The former have a mean whole-rock '18O value of 5.25ǂ.65‰ (1C), whereas the latter are much more variable, with a mean whole-rock '18O value of 3.00Dž.27‰. Biotite and amphibole separates from both granite types range in 'D from -69 to -116‰, and show a positive correlation with whole-rock '18O values. Dolerite dykes that intruded the granites during or shortly after their crystallization also have whole-rock '18O values (mean 2.24ǃ.93‰) lower than that expected for mantle-derived basaltic rocks, but these values appear to be the result of fluid-rock interaction. We suggest that the Mahé-type granites are derived mainly from juvenile mafic to intermediate crust with 'normal' 'D and '18O values, whereas the Praslin-type granites are mixtures of this source and older crust that acquired its low 'D and '18O values by extensive interaction with meteoric water at high temperature. It is unlikely that meteoric water sufficiently depleted in D and 18O was available at 750 Ma because of the relatively low latitude of the region at that time. We suggest that alteration of the source took place significantly before production of the granite magmas. Depletion in 18O of the Seychelles granites does not necessarily require a regional extensional tectonic setting at 750 Ma, as has been proposed.  相似文献   

8.
Products of voluminous pyroclastic eruptions with eruptive draw-down of several kilometers provide a snap-shot view of batholith-scale magma chambers, and quench pre-eruptive isotopic fractionations (i.e., temperatures) between minerals. We report analyses of oxygen isotope ratio in individual quartz phenocrysts and concentrates of magnetite, pyroxene, and zircon from individual pumice clasts of ignimbrite and fall units of caldera-forming 0.76 Ma Bishop Tuff (BT), pre-caldera Glass Mountain (2.1-0.78 Ma), and post-caldera rhyolites (0.65-0.04 Ma) to characterize the long-lived, batholith-scale magma chamber beneath Long Valley Caldera in California. Values of '18O show a subtle 1‰ decrease from the oldest Glass Mountain lavas to the youngest post-caldera rhyolites. Older Glass Mountain lavas exhibit larger (~1‰) variability of '18O(quartz). The youngest domes of Glass Mountain are similar to BT in '18O(quartz) values and reflect convective homogenization during formation of BT magma chamber surrounded by extremely heterogeneous country rocks (ranging from 2 to +29‰). Oxygen isotope thermometry of BT confirms a temperature gradient between "Late" (815 °C) and "Early" (715 °C) BT. The '18O(quartz) values of "Early" and "Late" BT are +8.33 and 8.21‰, consistent with a constant '18O(melt)=7.8ǂ.1‰ and 100 °C temperature difference. Zircon-melt saturation equilibria gives a similar temperature range. Values of '18O(quartz) for different stratigraphic units of BT, and in pumice clasts ranging in pre-eruptive depths from 6 to 11 km (based on melt inclusions), and document vertical and lateral homogeneity of '18O(melt). Worldwide, five other large-volume rhyolites, Lava Creek, Lower Bandelier, Fish Canyon, Cerro Galan, and Toba, exhibit equal '18O(melt) values of earlier and later erupted portions in each of the these climactic caldera-forming eruptions. We interpret the large-scale '18O homogeneity of BT and other large magma chambers as evidence of their longevity (>105 years) and convection. However, remaining isotopic zoning in some quartz phenocrysts, trace element gradients in feldspars, and quartz and zircon crystal size distributions are more consistent with far shorter timescales (102-104 years). We propose a sidewall-crystallization model that promotes convective homogenization, roofward accumulation of more evolved and stagnant, volatile-rich liquid, and develops compositional and temperature gradients in pre-climactic magma chamber. Crystal + melt + gas bubbles mush near chamber walls of variable '18O gets periodically remobilized in response to chamber refill by new hotter magmas. One such episode of chamber refill by high-Ti, Sr, Ba, Zr, and volatile-richer magma happened 103-104 years prior to the 0.76-Ma caldera collapse that caused magma mixing at the base, mush thawing near the roof and walls, and downward settling of phenocrysts into this hybrid melt.  相似文献   

9.
The Menderes Massif comprises an inner crystalline core with gneissic rocks and an outer surrounding schist belt with predominantly metasedimentary rocks. Both units have a complex metamorphic history including a late Alpine overprint. Temperatures inferred from oxygen isotope compositions of coexisting minerals increase from 420 to 600°C from the rim to the center. More positive '18O values in all minerals from the schist belt may reflect a higher abundance of sedimentary precursor material, whereas biotites and muscovites in core and rim are indistinguishable in hydrogen isotope composition. 'D values of muscovites range from -35 to -60‰, whereas 'D values of biotites range from -65 to -125‰, indicating normal values for muscovite but anomalously negative values for some biotites. For muscovite the trend can be interpreted in terms of increasing loss of water with rising metamorphic temperature. For biotite the 'D values decrease with increasing H2O content and decreasing Na2O+K2O content, which provides evidence for alteration processes or exchange of K and Na with water from interlayers of biotite forming hydro-biotite. The data suggest isotopic resetting of pre-Alpine characteristics during Alpine metamorphism. The hydrogen isotope composition of biotite was later disturbed, probably during extensional neotectonic movements in this region, as this allowed infiltration of and exchange with D-depleted meteoric water; however, the muscovites retained its Alpine characteristics.  相似文献   

10.
Quartz diorites represent the earliest (ca. 540 Ma) and most primitive plutonic rocks in the Pan African Damara belt and they pre-date the main phase of high-T regional metamorphism. Two suites of synorogenic quartz diorites are unusual among Damaran intrusive rocks in their elemental and isotopic features. Comparison of the diorite compositions with melts from amphibolite-dehydration melting experiments points to a garnet-bearing meta-tholeiite, probably enriched in K2O, as a likely source rock. Partial melting processes generated mafic (ca. 50 wt% SiO2) quartz diorites in the deep crust at temperatures of between 1,000 and 1,100 °C, based on comparison with experimental results and similar temperature estimates based on P2O5 solubility in mafic rocks. Subsequently, the quartz diorites evolved by multistage, polybaric differentiation processes including fractional crystallization of mainly hornblende and plagioclase and assimilation of felsic basement gneisses. Although their chemical characteristics (high LILE, low HFSE) resemble those of other quartz diorites with calc-alkaline affinities, they differ in their enriched Sr (initial 87Sr/86Sr: 0.70943-0.71285), Nd (initial ) Nd: -9.1 to -15.2 ) and O ('18O: 6.8-8.1‰) isotope compositions. Neodymium model ages (TDM) that range from 1.7 to 2.2 Ga and large variation in 207Pb/204Pb relative to 206Pb/204Pb indicates involvement of ancient crustal material. Lead (206Pb/204Pb: 17.08-17.23, 207Pb/204Pb: 15.53-15.62, 208Pb/204Pb: 37.71-38.16) isotope compositions are strongly retarded, indicating that the source underwent a pre-Pan-African U/Pb fractionation and U depletion. It is proposed that the quartz diorites originated by synorogenic high temperature melting of mafic lower crust. This contrasts with previous suggestions favouring an origin of these rocks by melting of an enriched mantle during Pan-African times with characteristics modified by subduction of oceanic crust and sedimentary rocks.  相似文献   

11.
The Bixiling mafic-ultramafic metamorphic complex is a 1•5km2 tectonic block within biotite gneiss in the southern Dabieultrahigh-pressure terrane, central China. The complex consistsof banded eclogites that contain thin layers of garnet-bearingcumulate ultramafic rock. Except for common eclogitic phases(garnet, omphacite, kyanite, phengite, zoisite and rutilc),banded eclogites contain additional talc and abundant coesiteinclusions in omphacite, zoisite, kyanite and garnet. Some metaultramaficrocks contain magnesite and Ti-clinohumite. Both eclogites andmeta-ultramafic rocks have undergone multi-stage metamorphism.Eclogite facies metamorphisrn occurred at 610–700C andP>27 kbar, whereas amphibolite facies retrograde metamorphismis characterized by symplectites of plagioclase and hornblendeafter omphacite and replacement of tremolite after talc at P<6–15kbar and T <600C. The meta-ultramafic assemblages such asolivine + enstatite + diopside + garnet and Ti-clinohumite +diopside + enstatite + garnet + magnesite olivine formed at700–800C and 47–67 kbar. Investigation of the phaserelations for the system CaO-MgO-SiO2-H2O-CO2 and the experimentallydetermined stabilities of talc, magnesite and Ti-clinohumiteindicate that (1) UHP talc assemblages are restricted to Mg-Algabbro composition and cannot be an important water-bearingphase in the ultramafic mantle, and (2) Ti-clinohumite and magnesiteare stable H2O-bearing and CO2-bearing phases at depths >100km. The mafic-ultramafic cumulates were initially emplaced atcrustal levels, then subducted to great depths during the Triassiccollision of the Sine-Korean and Yangtze cratons. KEY WORDS: eclogite; magnesite; meta-ultramafics; talc; ultrahigh-P metamorphism *Corresponding author  相似文献   

12.
Stable carbon isotope ratios in the organic fraction of surface sediments from the Laptev Sea shelf were analyzed in order to study the modern distribution pattern of terrestrial organic matter. The '13Corg signature of the surface sediments range from -26.6‰ near the coastal margin to -22.8‰ in the north towards the outer shelf. Characterizing the possible sources of organic matter by their '13Corg signature reveals that the terrestrial influence reaches further north in the eastern than in the western Laptev Sea. Downcore records of the '13Corg, measured on three AMS 14C-dated cores from water depths between 46 and 77 m, specify the spatial and temporal changes in the deposition of terrestrial organic matter on the Laptev Sea shelf during the past 12.7 ka. The major depositional changes of terrestrial organic matter occurred between 11 and 7 ka and comprised the main phase of the southward retreat of the coastline and of the river depocenters due to the postglacial sea level rise.  相似文献   

13.
Stable sulfur and oxygen isotope ratios and naturally occurring 35SSO4 activities were used to examine sulfate sources, address the role of sulfur dynamics, and estimate residence times of atmospherically derived sulfate in Loch Vale Watershed, Colorado. In 1996, surface water samples from small streams flowing through talus, forest, and wetland areas had '34SSO4 values ranging from 1.8 to 3.7‰. Values of '18OSO4 at the three sites ranged from -1.3 to 3.7‰. Average '34SSO4 and '18OSO4 values in Loch Vale precipitation (1991-1999) are higher (5.2 and 13.6, respectively) than surface water values, indicating that some of the deposited sulfate is transformed and/or mixed with other sulfur sources in the watershed (e.g. mineral and organic sulfur). Sulfate ages determined by 35SSO4 activities support this and show that deposited sulfate may be stored on a timescale of 1 year or more prior to being released to surface waters.  相似文献   

14.
Organic matter origins are inferred from carbon isotope ratios ('13C) in recent continental shelf sediments and major rivers from 465 locations from the north Bering-Chukchi-East Siberian-Beaufort Sea, Arctic Amerasia. Generally, there is a cross-shelf increase in '13C, which is due to progressive increased contribution seaward of marine-derived organic carbon to surface sediments. This conclusion is supported by the correlations between sediment '13C, OC/N, and '15N. The sources of total organic carbon (TOC) to the Amerasian margin sediments are primarily from marine water-column phytoplankton and terrigenous C3 plants constituted of tundra taiga and angiosperms. In contrast to more temperate regions, the source of TOC from terrigenous C4 and CAM plants to the study area is probably insignificant because these plants do not exist in the northern high latitudes. The input of carbon to the northern Alaskan shelf sediments from nearshore kelp community (Laminaria solidungula) is generally insignificant as indicated by the absence of high sediment '13C values (-16.5 to -13.6‰) which are typical of the macrophytes. Our study suggests that the isotopic composition of sediment TOC has potential application in reconstructing temporal changes in delivery and accumulation of organic matter resulting from glacial-interglacial changes in sea level and environments. Furthermore, recycling and advection of the extensive deposits of terrestrially derived organic matter from land, or the wide Amerasian margin, could be a mechanism for elevating total CO2 and pCO2 in the Arctic Basin halocline.  相似文献   

15.
Diffusion-controlled growth rates of polycrystalline enstatite reaction rims between forsterite and quartz were determined at 1,000 °C and 1 GPa in presence of traces of water. Iron-free, pure synthetic forsterite with normal oxygen and silicon isotopic compositions and quartz extremely enriched in 18O and 29Si were used as reactants. The relative mobility of 18O and 29Si in reactants and rims were determined by SIMS step scanning. The morphology of the rim shows that enstatite grows by a direct replacement of forsterite. Rim growth is modelled within a mass-conserving reference frame that implies advancement of reaction fronts from the initial forsterite-quartz interface in both directions. The isotopic compositions at the two reaction interfaces are controlled by the partial reactions Mg2SiO4=0.5 Mg2Si2O6+MgO at the forsterite-enstatite, and MgO+SiO2=0.5 Mg2Si2O6 at the enstatite-quartz interface, implying that grain boundary diffusion of MgO is rate-controlling. Isotopic profiles show no silicon exchange across the propagating reaction interfaces. This propagation, controlled by MgO diffusion, is faster than the homogenisation of Si by self-diffusion behind the advancing fronts. From this, and using % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn % hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr % 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9 % vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x % fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamiramaaDa % aaleaacaWGtbGaamyAaiaacYcacaWGfbGaamOBaaqaaiaadAfacaWG % VbGaamiBaaaaaaa!3DD2! DSi,EnVolD_{Si,En}^{Vol} at dry conditions from the literature, results a % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn % hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr % 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9 % vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x % fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmirayaafa % Waa0baaSqaaiaadofacaWGPbGaaiilaiaadweacaWGUbaabaaaaOGa % eqiTdqgaaa!3CCD! D￠Si,En dD'_{Si,En}^{} \delta value of 3᎒-24 m3 s-1 at 1,000 °C. The isotopic profiles for oxygen are more complex. They are interpreted as an interplay between the propagation of the interfaces, the homogenisation of the isotope concentrations by grain boundary self-diffusion of O within the rim, and the isotope exchange across the enstatite-quartz interface, which was open to 18O influx from quartz. Because of overlapping diffusion processes, boundary conditions are unstable and D´Ox,En' cannot be quantified. Using measured rim growth rates, the grain boundary diffusivity D´MgO' of MgO in iron-free enstatite is 8᎒-22 m3 s-1 at 1,000 °C and 1 GPa. Experiments with San Carlos olivine (fo92) as reactant reveal lower rates by a factor of about 4. Our results show that isotope tracers in rim growth experiments allow identification of the actual interface reactions, recognition of the rate-controlling component and further calculation of D´' values for specific components.  相似文献   

16.
Superdeep diamonds from the Juina area, Mato Grosso State, Brazil   总被引：4，自引：1，他引：3  
Alluvial diamonds from the Juina area in Mato Grosso, Brazil, have been characterized in terms of their morphology, syngenetic mineral inclusions, carbon isotopes and nitrogen contents. Morphologically, they are similar to other Brazilian diamonds, showing a strong predominance of rounded dodecahedral crystals. However, other characteristics of the Juina diamonds make them unique. The inclusion parageneses of Juina diamonds are dominated by ultra-high-pressure ("superdeep") phases that differ both from "traditional" syngenetic minerals associated with diamonds and, in detail, from most other superdeep assemblages. Ferropericlase is the dominant inclusion in the Juina diamonds. It coexists with ilmenite, Cr-Ti spinel, a phase with the major-element composition of olivine, and SiO2. CaSi-perovskite inclusions coexist with titanite (sphene), "olivine" and native Ni. MgSi-perovskite coexists with TAPP (tetragonal almandine-pyrope phase). Majoritic garnet occurs in one diamond, associated with CaTi-perovskite, Mn-ilmenite and an unidentified Si-Mg phase. Neither Cr-pyrope nor Mg-chromite was found as inclusions. The spinel inclusions are low in Cr and Mg, and high in Ti (Cr2O3<36.5 wt%, and TiO2>10 wt%). Most ilmenite inclusions have low MgO contents, and some have very high (up to 11.5 wt%) MnO contents. The rare "olivine" inclusions coexisting with ferropericlase have low Mg# (87-89), and higher Ca, Cr and Zn contents than typical diamond-inclusion olivines. They are interpreted as inverted from spinel-structured (Mg, Fe)2Si2O4. This suite of inclusions is consistent with derivation of most of the diamonds from depths near 670 km, and adds ilmenite and relatively low-Cr, high-Ti spinel to the known phases of the superdeep paragenesis. Diamonds from the Juina area are characterized by a narrow range of carbon isotopic composition ('13C=-7.8 to -2.5‰), except for the one majorite-bearing diamond ('13C=-11.4‰). There are high proportions of nitrogen-free and low-nitrogen diamonds, and the aggregated B center is predominant in nitrogen-containing diamonds. These observations have practical consequences for diamond exploration: Low-Mg olivine, low-Mg and high-Mn ilmenite, and low-Cr spinel should be included in the list of diamond indicator minerals, and the role of high-Cr, low-Ti spinel as the only spinel associated with diamond, and hence as a criterion of diamond grade in kimberlites, should be reconsidered.  相似文献   

17.
Mafic granulite xenoliths from the lower crust of the Pannonian Basin are dominated by LREE-depleted bulk-rock compositions. Many of these have MORB-like 143Nd/144Nd but 87Sr/86Sr is elevated relative to most MORBs. Their '18O values cover a wide range from +3.8 to +9.5‰. A group of LREE-enriched mafic granulites have higher 87Sr/86Sr (0.704-0.708) and lower 143Nd/144Nd (0.5128-0.5124), with higher '18O values on average (+7.8 to +10.6‰) than the LREE-depleted granulites. The LREE-enriched granulites are, however, isotopically similar to newly discovered metasedimentary granulite xenoliths. A sublinear correlation in )Hf-)Nd isotope space has a shallower slope than the crust-mantle array, with the metasedimentary rocks forming the low )Hf end member; the radiogenic end is restricted to the LREE-depleted granulites and these overlap the field of MORB. Pb isotopes for the LREE-depleted samples are less radiogenic on average than those of the LREE-enriched and metasedimentary xenoliths, and metasedimentary granulites have consistently higher 208Pb/204Pb. The wide range in '18O over a restricted range in Nd and Sr isotope values, in combination with the predominance of LREE-depleted trace-element compositions, is consistent with an origin as a package of hydrothermally altered oceanic crust. The existence of '18O values lower than average MORB and/or mantle peridotite requires that at least some of these rocks were hydrothermally altered at high temperature, presumably in the oceanic lower crust. The low 143Nd/144Nd of the LREE-enriched mafic granulites cannot be explained by simple mixing between a LREE-depleted melt and an enriched component, represented by the recovered metasediments. Instead, we interpret these rocks as the metamorphic equivalent of the shallowest levels of the ocean crust where pillow basalts are intimately intercalated with oceanic sediments. A possible model is accretion of oceanic crustal slices during subduction and convergence, followed by high-grade metamorphism during the Alpine orogeny.  相似文献   

18.
Although general accounts of carbonatites usually envisage Ca-Mg carbonate melts evolving by fractional crystallisation to Fe-rich residua, there is longstanding concern that ferrocarbonatites may actually be products of hydrothermal rather than magmatic processes. All previously published examples of ankerite- and/or siderite-carbonatites fail to show one or more of the isotopic criteria (all determined on the same sample) thought to be diagnostic of crystallised magmatic carbonate liquids. Ferrocarbonatite dykes cut Archaean-Proterozoic basement at Swartbooisdrif, adjacent to the NW Namibia-Angola border. Their age is uncertain but probably ~1,100 Ma and their associated fenites are rich in sodalite. Where unaffected by subsequent recrystallisation, their petrographic textures resemble those of silicate layered intrusions; ankerite, magnetite and occasionally calcite are cumulus phases, joined by trace amounts of intercumulus pyrochlore. Ankerite is zoned, from Ca(Mg, Fe2+)(CO3)2 cores towards ferroan dolomite rims. Calcite contains ~1.7% SrO, plus abundant, tiny exsolved strontianite grains. Magnetite is close to pure Fe3O4. Pyrochlore has fine-scale euhedral oscillatory zoning and light-REE-enriched rims. ICP-MS analysis of magnetite and pyrochlore from the carbonatite allows calculation of their modal amounts from mass-balance considerations. Sodalite from the fenite is REE poor. Geothermometry, using either the calcite-dolomite solvus or oxygen isotope fractionation between calcite and magnetite, gives temperatures in the range 420-460 °C. Initial Sr, Nd and Pb isotopic ratios of the ferrocarbonatites (87Sr/86Sr=0.7033; )Nd=0.2-1.0; 206Pb/204Pb=16.37; 207Pb/204Pb=15.42; 208Pb/204Pb=36.01) are appropriate for an ~1,100-Ma magmatic carbonatite. Likewise, carbonate '18O=8.0 and '13C=-7.36 indicate little or no subsequent shift from magmatic values. It appears that dense ankerite and magnetite dominated crystal accumulation from a melt saturated in these phases, plus calcite and pyrochlore, with prior fractionation of a silicate mineral and apatite. The resulting ferrocarbonatite lacks a silicate mineral (excluding fenite xenocrysts) and apatite. It has unusually low (basalt-like) REE abundances and (La/Lu)n, and low concentrations of Ba, Rb, U, Th, Nb, Ta, Zr and Hf. Very high Nb/Ta and low Zr/Hf imply that the evolution of the parental magma involved immiscible separation of a carbonate from a silicate melt. The sodalite-dominated Swartbooisdrif fenites suggest that the parental melt also had a substantial Na content, in contrast with the ferrocarbonatite rock.  相似文献   

19.
Stable isotope data (δ18O, δ13C) were obtained for magnesite (MgCO3) from Holocene salt lake deposits of the Taoudenni–Agorgott basin, Mali, in which it is the only carbonate mineral present. The deposits have a high glauberite content (Na2Ca(SO4)2), representing a type of continental evaporite formation that is commonly magnesite‐bearing. Samples from seven different levels in a 5 m long sequence were analysed. δ18OV‐PDB values are between +3.17 and +5.91‰, which is lower than might be expected for evaporitic environments, recording reduced 18O enrichment at high salinity. δ13CV‐PDB values are between −1.32‰ and −4.79‰, showing an influence of carbon derived from the decomposition of organic matter rather than from exchange with atmospheric CO2. Covariance between δ18O and δ13C is strong for the lower part of the sequence, recording coupled 18O and 13C enrichment as commonly observed for closed basins. Covariance is lacking for the upper part of the sequence, with only periodic massive magnesite deposition in a more shallow lake. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

20.
采用野外观察、室内薄片鉴定及多项地球化学分析技术方法,对塔里木盆地柯坪地区上寒武统表生溶蚀型藻格架白云岩的特征及成因进行了研究。宏观上,藻格架白云岩呈丘状、透镜状夹于潮坪相白云岩层间,由于差异性溶蚀,发育了大量表生溶蚀孔。微观上,藻格架由富藻的泥粉晶白云石组成,而架间孔由浅色的亮晶白云石充填。藻格架泥粉晶白云石呈他形—半自形,镶嵌结构,具有暗红色—橙红色的阴极发光,较高的Na、K含量,较低的Fe含量;δ13C为-0.572‰～0.124‰、平均值-0.116‰,δ18O为-5.391‰～-4.983‰、平均值-5.240‰,表明其形成于准同生阶段盐度较高的相对氧化环境中。架间充填的亮晶白云石胶结物,呈半自形—自形中细晶,具有昏暗的阴极发光或者不发光,较低的Na、K含量,较高的Fe含量,δ13C值为-0.662‰～-0.251‰、平均值为-0.460‰;δ18O值为-6.639‰～-5.939‰、平均值-6.267‰,表明其形成于相对还原的埋藏环境。稀土元素分析结果表明,二者均具有LREE轻微富集、HREE亏损、Eu负异常特征,与海相泥晶灰岩稀土元素配分模式相似,揭示了其白云化流体均来自于原始的海水。在溶蚀作用方面,亮晶白云石胶结物相对泥粉晶白云石藻格架更易于溶蚀。前者在大气水表生溶蚀过程中,主量元素Ca、Mg丢失显著,Mg/Ca值由0.955降至0.007,微量元素Na、K丢失相对明显,Na/Ca值由原来的3.8×10-4降为1.9×10-4,K/Ca值由1.1×10-3降至检测限以下,而不改变稀土元素的配分模式。这些特征表明,表生溶蚀过程在元素特征上是一个去白云化的盐度降低过程,而这一过程中基本无稀土元素的带入带出。  相似文献   

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