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1.
The deposit under study is a hydrothermal filling-metasomatic vein type lead-zinc-silver deposit, in whichgold and silver can be recovered as by-products. These metals mainly occur as microgranular native gold,electrum, stephanite, acanthite, pyraragyrite, freibergite, and native silver. Gold minerals tend to be associatedwith galenobismutite, native bismuth and unnamed Bi_2Te. They are either enclosed in pyrite, marmatite,iron-bearing sphalerite and galens or fill the microfissures of these minerals. Silver minerals usually occur incleavages or fissures of galena, marmatite and pyrite, but are not associated with gold and bismuth minerals.Gold and silver mineralizations occurred later than lead and zinc, while the silver mineralization was precededby that of gold. 相似文献
2.
B. G. Pokrovsky P. O. Zaviyalov M. I. Bujakaite A. S. Izhitskiy O. L. Petrov A. K. Kurbaniyazov V. M. Shimanovich 《Geochemistry International》2017,55(11):1033-1045
The paper presents original authors' data on the O, H, C, S, and Sr isotopic composition of water and sediments from the basins into which the Aral Sea split after its catastrophic shoaling: Chernyshev Bay (CB), the basin of the Great Aral in the north, Lake Tshchebas (LT), and Minor Sea (MS). The data indicate that the δ18О, δD, δ13C, and δ34S of the water correlate with the mineralization (S) of the basins (as of 2014): for CB, S = 135.6‰, δ18О = 4.8 ± 0.1‰, δD = 5 ± 2‰, δ13C (dissolved inorganic carbon, DIC) = 3.5 ± 0.1‰, δ34S = 14.5‰; for LT, S = 83.8‰, δ18О = 2.0 ± 0.1‰, δD =–13.5 ± 1.5‰, δ13C = 2.0 ± 0.1‰, δ34S = 14.2‰; and for MS, S = 9.2‰, δ18О =–2.0 ± 0.1‰, δD =–29 ± 1‰, δ13C =–0.5 ± 0.5‰, δ34S = 13.1‰. The oxygen and hydrogen isotopic composition of the groundwaters are similar to those in MS and principally different from the artesian waters fed by atmospheric precipitation. The mineralization, δ13С, and δ34S of the groundwaters broadly vary, reflecting interaction with the host rocks. The average δ13С values of the shell and detrital carbonates sampled at the modern dried off zones of the basins are similar: 0.8 ± 0.8‰ for CB, 0.8 ± 1.4‰ for LT, and –0.4 ± 0.3‰ for MS. The oxygen isotopic composition of the carbonates varies much more broadly, and the average values are as follows: 34.2 ± 0.2‰ for CB, 32.0 ± 2.2‰ for LT, and 28.2 ± 0.9‰ for MS. These values correlate with the δ18O of the water of the corresponding basins. The carbonate cement of the Late Eocene sandstone of the Chengan Formation, which makes up the wave-cut terrace at CB, has anomalously low δ13С up to –38.5‰, suggesting origin near a submarine methane seep. The δ34S of the mirabilite and gypsum (11.0 to 16.6‰) from the bottom sediments and young dried off zone also decrease from CB to MS in response to increasing content of sulfates brought by the Syr-Darya River (δ34S = 9.1 to 9.9‰) and weakening sulfate reduction. The 87Sr/86Sr ratio in the water and carbonates of the Aral basins do not differ, within the analytical error, and is 0.70914 ± 0.00003 on average. This value indicate that the dominant Sr source of the Aral Sea is Mesozoic–Cenozoic carbonate rocks. The Rb–Sr systems of the silicate component of the bottom silt (which is likely dominated by eolian sediments) of MS and LT plot on the Т = 160 ± 5 Ma, I0 = 0.7091 ± 0.0001, pseudochron. The Rb–Sr systems of CB are less ordered, and the silt is likely a mixture of eolian and alluvial sediments. 相似文献
3.
Among several lithostratigraphic subdivisions of the Gaj Formation of Miocene age, the Jhill limestone is entirely different
with respect to its colour, texture and structures. This limestone unit has been evaluated to elaborate its geochemical and
sedimentological characteristics. The distribution of various elements in the acid-soluble fraction has been studied in order
to determine their mineralogy, sedimentary environment, facies and diagenesis. Mineralogy, recrystallization and other diagenetic
changes are the main factors affecting the distribution of trace elements and their mutual relationships in the limestones.
Samples of the Jhill limestone show depletion in large-sized ions (Sr, Pb & K) and also in the ions that are not compatible
with calcite space group. Elements (Fe, Mn, Zn, Cu & Co) having distribution coefficient (D) above unity for natural calcites,
are more enriched. Microscopic and X-ray studies revealed nearly complete conversion of aragonite into stable low-Mg calcite.
An attempt has also been made to verify the reefal conditions for these limestones on the basis of geochemical studies. The
plots of Sr and other facies-indicator elements show that the majority of the beds belong to forereef flank facies with some
algal banks. Low Mg/Ca and Sr/Ca ratios suggest that a phreatic diagenetic environment prevailed after the deposition. High
concentrations of Cr, Ni, and Co in the Jhill limestone show a positive correlation with a higher amount of insoluble residue,
which reflects a relatively high rate of influx of terrigenous material. 相似文献
4.
5.
The characteristic structures of the Precambrian cherts from the Gusui section, Guangdong ,Chi-na, include bedded structure ,laminated structure ,massive structure and pseudobrecciated structure.The chert is characterized by consistently low abundance of TiO2,Al2O3 and most trace elements.Howevver ,it is enriched in Ba,As,Sb,Hg and Se.In Al-Fe-Mn ternary diagrams,it falls into the “hydrothermal field“ .Correspondence analysis and factor analysis show that many elements show up in the factor that represents the leaching of country rocks by hydrothermal solutions,and are the very characteristic element association fo the geochemically anomalous South China basement.Petrologic and geochemical evidence suggests a hydrothermal origin for the chert.The chert may have been formed in a Precambrian fift or an extension zone developed within the Yunkai marginal geosyncline, with a fault system linking it to an unknown heat source at depth. 相似文献
6.
This study is aimed at determining the diffusion coefficient of net-work modifiers (mainly Na, K, and Ca) in a two-phase melt-NaCl
system, in which the melts are granitic and the system is NaCl-rich in composition. The diffusion coefficients of Na, K, and
Ca were measured at the temperatures of 750 – 1400°C, pressures of 0.001 × 108 – 2 × 108 Pa, and initial H2O contents of 0 wt% –6.9 wt% in the granitic melts. The diffusion coefficients of Fe and Mg were difficult to resolve. In
all experiments a NaCl melt was present as well. In the absence of H2O, the diffusion of net-work modifiers follows an Arrhanious equation at 1 × 105 Pa: lgDca=−3. 88−5140/T, lgDk =−3. 79−4040/T, and lgDNa, =−4.99−3350/T, where D is in cm2 /s andT is in K. The diffusion coefficients of Ca, Na, K, and Fe increase non-linearly with increasing H2O content in the melt. The presence of about 2 wt% H2O m the melt will lead to a dramatical increase in diffusivity, but higher H2O content has only a minor effect. This change is probably the result of a change in the melt structure when H2O is present. The diffusion coefficients measured in this study are significantly different from those in previous works.
This may be understood in terms of the “transient two-liquid equilibrium” theory. Element interdiffusion depends not only
on its concentration, but also on its activity co-efficient gradient, which is reflected by the distribution coefficient,
of the two contacting melts. 相似文献
7.
《International Geology Review》2012,54(5):379-420
Variations in the abundances of Zn, Cu, and Pb are found to be useful in identifying tectonic regimes and separating oceanisland basalts into enriched- and depleted-source categories. The average Zn, Cu, and Pb contents of normal mid-ocean ridge basalts (N-MORB) are 84, 70, and 0.35 ppm, respectively. Differences in average Zn contents for various ridges reflect more the varying degrees of differentiation than variations of Zn content in the source rocks. At a Mg# of 70, or Mg#70, which is taken to represent primitive MORB, many MORB sequences converge at a Zn content of 58 ± 6 ppm, which is close to the value for primitive mantle (50 ppm) and ordinary chondrites (~55 ppm). Values of 0.1 to 0.15 ppm Pb in MORB at Mg#70, best defined at the superfast-spreading Southern East Pacific Rise, are similar to estimates of Pb in the primitive mantle (0.12 to 0.18 ppm). They also are near the lower end of the range for ordinary chondrites. The very slow spreading Southwest Indian Ocean Ridge has a sequence with higher Pb contents, in addition to a more normal sequence, which has a visual best value of 0.4 ppm Pb at Mg#70. With the exception of the Walvis Ridge, Zn and Cu appear to be little affected by proximity to hotspots (i.e., E-MORB); however, Pb contents are higher and average about 0.6 ppm. Both Zn and Pb in MORB are incompatible elements (i.e., favor the melt), but Cu is a compatible element. At Mg#70, there is the suggestion of a value of 100 ppm for Cu, with lower values possibly representing partial removal of sulfides and their associated Cu from the source. Nonetheless, Cu contents of primitive MORB tend to be much higher than even high estimates for the primitive mantle (28 ppm), and are closer to ordinary chondrites (~90 ppm). Therefore, Zn, Cu, and Pb all approximate chondritic values in the primitive MORB melt. Average contents of Zn, Cu, and Pb in oceanic island basalts (OIB) are 115, 62, and 3.2 ppm, respectively. At Mg#70, values of Zn and Cu are similar to the respective averages for OIB, with Zn higher and Cu lower than MORB. At a Mg# of ~40, however, OIB and MORB tend to have similar Zn contents. With further differentiation, OIB trachytes can contain >200 ppm Zn. Unlike MORB, OIB can differentiate to high Cu contents of 200 ppm at Mg#s of 40 to 60. In contrast to Zn and Cu, Pb regresses to a value of 0.83 ppm at Mg#70 for Hawaiian and Reunion volcanics, which is much less than the average value for Pb in OIB volcanics, but higher than for MORB. Average Zn, Cu, and Pb contents of magmatic-arc basalts are 77, 108, and 1.9 ppm, respectively. In basalts, Zn tends to be incompatible, but a dual incompatible and compatible behavior can occur at high SiO2 contents. Dacites may average near 55 ppm Zn, but peralkalic rhyolite can contain >300 ppm Zn. A dual compatible and incompatible nature occurs for Cu. Most common, particularly in submarine volcanics, is a compatible trend, with a Cu content of around 80 ppm at a Mg# of 60, which decreases to less than 40 ppm at a Mg# of 30. The incompatible trend of increasing Cu can achieve >200 ppm at a Mg# of 30, leaving a gap approaching 100 ppm at that Mg#. The gap is less obvious on a plot of Cu vs. SiO2, but is still there. The compatible trend is proposed to result from sulfur-saturated magmas, whereas the incompatible trend is believed to result from sulfur-deficient magmas. Support for this hypothesis is found in sparse sulfur-isotope data. Zn and Cu both can be incompatible over an extended range of Mg#s or silica content. When Zn and Cu are both compatible, Cu decreases more than twice as rapidly as Zn. Primitive magmas at Mg#70 average about 50 ppm Zn for submarine Mariana arc basalts and 58 ppm for forearc boninites, contents close to MORB values. Mariana arc basalts have a Zn content of ~45 ppm estimated at Mg#70. Cu varies more widely than Zn in primitive magmas, being about 50 ppm Cu for Mariana Islands volcanics and 120 ppm for Kermadec Islands volcanics, a range broadly around MORB values. Average Pb contents are 1.9 ppm for island-arc tholeiites, 5.6 ppm for high-Al basalt, and 3.2 ppm for alkali basalt with average boninite of approximately 1.8 ppm. Back-arc-basin basalts in the deepest parts of the Mariana trough have Pb contents of 0.45 ppm, but more shallow parts may exceed 1.0 ppm Pb. Although the lower contents are similar to MORB values, the 208Pb/204Pb values are greater than Pacific Ocean MORB. At Mg#70 for rocks from the Tonga and Kermadec island arcs, the Pb content is about 0.1 ppm, similar to MORB. 相似文献
8.
9.
A.E.KELEPERTSIS E.KONTIS 《中国地球化学学报》1997,16(1):8-19
The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite. 相似文献
10.
Liping ZHANG Rongshu ZENG 《中国地球化学学报》2006,25(B08):38-39
Three dumping sites have been formed at the northern region of Fushun City, Liaoning Province, for a large number of gangues including much oil shale that had been piled onto ground as gangue during long-term coal exploitation at West Fushun Open-pit Mine. Under appropriate conditions, self-combustion occurs after long-term exposure of oil shale and consequently such phenomena could be found almost everywhere at the three dumping sites. Much polycyclic aromatic hydrocarbons (PAHs) must be generated through oil shale self-combustion, a kind of incomplete combustion. In this paper, in order to make clear the PAHs distribution in oil shale and its self-combustion and their potential effects on surrounding environment, coal, low-grade oil shale, high-grade oil shale, burning oil shale, burnt oil shale and shaly soil collected from West Fushun Open-Pit Mine and West Dumping Site were analyzed quantitatively in 16 US EPA priority PAHs for the first time. Results showed that 16 PAHs in all samples were less than those in some bitumites and carbonaceous coals and were as much as those in lignites and anthracites from some Chinese mining areas. Coal and low-grade oil shale were abundant in lower molecular-weighted PAHs in contrast to high-grade oil shale with rich higher molecular-weighted PAHs. They had more benzo[a] pyrene than the highest background value in soils in Liaoning Province. So PAHs in these crude oil shales could cause potential effects on environment. There were at least 5121.40 p.g/kg PAils generated and at least 3976.70 μg/kg PAHs released into environment in the period from combustion beginning to sampling on the basis of calculation. Furthermore, the concentrations of 3-4 ring PAHs among them were very high. Therefore it could be said that oil shale self-combustion aggravated the environmental impacts of PAHs in oil shale. The low concentrations of PAHs in shaly soil showed that much PAHs had been released through recultivation and biodegradation. 相似文献
11.
Volcán Ceboruco, Mexico, erupted ~1,000 years ago, producing the Jala pumice and forming a ~4-km-wide caldera. During that eruption, 2.8 to 3.5 km3 of rhyodacite (~70 wt% SiO2) magma and 0.2 to 0.5 km3 of mixed dacite (~67 wt% SiO2) magma were tapped and deposited as the Jala pumice. Subsequently, the caldera was partially filled by extrusion of the Dos Equis dome, a low-silica (~64 wt% SiO2) dacite dome with a volume of ~1.3 km3. Petrographic evidence indicates that the Jala dacite and Dos Equis dacite originated largely through the mixing of three end-member magmas: (1) rhyodacite magma, (2) dacite magma, and (3) mafic magma. Linear least-squares modeling and detailed modal analysis indicate that the Jala dacite is predominantly a bimodal mixture of rhyodacite and dacite with a small additional mafic component, whereas the Dos Equis dacite is composed of mostly dacite mixed with subordinate amounts of rhyodacite and mafic magma. According to Fe–Ti oxide geothermometry, before the caldera-forming eruption the rhyodacite last equilibrated at ~865 °C, whereas the dacite was originally at ~890 °C but was heated to ~960 °C by intrusion of mafic magma as hot as ~1,030 °C. Zoning profiles in plagioclase and/or magnetite phenocrysts indicate that mixing between mafic and dacite magma occurred ~34–47 days prior to eruption, whereas subsequent mixing between rhyodacite and dacite magmas occurred only 1–4 days prior to eruption. Following the caldera-forming eruption, continued inputs of mafic magma led to effusion of the Dos Equis dome dacite. In this case, timing between mixing and eruption is estimated at ~93–185 days based on the thickness of plagioclase overgrowth rims.Editorial responsibility: T.L. Grove 相似文献
12.
Idu–Karmo of the federal capital territory, Abuja, is located within the weathered basement aquifers of Northern Nigeria. Fifteen groundwater samples obtained were analysed for their major ionic components. The physical properties show that the water is slightly acidic to neutral (6.0–7.0) and has moderate to very high values of electrical conductivity (155–2230 µS/cm).The dominant hydrochemical facies of groundwater is the Ca–Cl2 groundwater type. Irrigation parameters measured include: SAR which ranges from 0.12 to 1.06; TH which ranges from 0.8 to 196; KR ranges from 0.03 to 0.42; PI which ranges from 46 to 199; and RSC ranges from ??131.90 to 3.43. These parameters (SAR, total hardness, Kelly’s ratio, permeability index and residual sodium carbonate) show that the water is suitable for agricultural purpose except for the magnesium ratio which has a high unsuitability for irrigation, probably due to the presence of ferro-magnesian minerals contained in the calc-alkaline basement rocks of the Idu–Karmo area. The results of the geochemical survey reveal major ionic components are in the order Cl??>?HCO3??>?NO3??>?SO42? and Mg2+?>?Ca2+?>?Na+?>?K+. Comparison with WHO and APHA standards shows that all the ionic concentrations satisfy all permissible limits for drinking purpose except for elevated concentrations of nitrate which probably may have arisen from poor handling of domestic wastes, leakages from nearby septic tanks/soak-away and the excessive use of fertilisers. Qualitatively, treatment is required especially on the nitrate-contaminated areas to make the water fit for drinking and irrigation. 相似文献
13.
Zhuang Hanping Institute of Geochemistry Chinese Academy of Sciences Guiyang GuizhouRan Chongying He Mingqin Geology Department Kunming Institute of Technology Kunming Yunnanand Lu Jialan Guangzhou Institute of Geochemistry Chinese Academy of Sciences Guangdong 《《地质学报》英文版》1996,70(4):407-419
Studies on organic geochemistry indicate that the origin, type and maturity of organic matter are different among coal-bearing, copper-bearing and evaporite formations in the Mesozoic continental Chuxiong Basin, Yunnan, China. A mechanism has been proposed that (1) during the diagenetic mineralization stage the short-chain organic acids dervied from kerogen played an important role in remobilizing copper from source beds, while oils acted as important carrier of copper, and that (2) during the transformation or remolding mineralization stage, meteoric water leached the evaporite layers and formed downward-percolating oxidizing SO42-rich fluids; meanwhile, the copper-bearing fluids migrating upwards along growth faults from the basement was contaminated by the coal-bearing series on the way and formed reducing organic-rich fluids; oxidation-reduction occurred and sulfides formed when the two kinds of fluids met within sandstones. 相似文献
14.
On the basis of an experimental study and thermodynamic calculation, the mechanisms of paragenesis and separation of silver, lead and zinc in the hydrothermal system have been studied. At acidic to nearly neutral pH, their chloride complexes are stable, and among them the chloride complexes of zinc are most stable. And the sulfide complexes are the dominant species at nearly neutral to alkaline pH,while the sulfide complexes of silver are most stable. With decreasing temperature, [ Cl^-] ,fO2, and increasing pH, the solubilities of silver, lead and zinc will decrease, leading to their deposition and separation. For sulfide complexes, the concentrations of reduced sulfur and pH are two important factors affecting their stabilities. Complexes of different forms and stabilities respond to the variation of conditions to different extents, which gave rise to the paragenesis and separation of silver, lead and zinc in the whole ore-forming process of dissolution, transport and deposition. 相似文献
15.
K-Ar ages of illite-muscovite and fission track ages of zircon and apatite were determined from various lithotypes of the Bükkium, which forms the innermost segment of the Western Carpathians. The stratigraphic ages of these Dinaric type formations cover a wide range from the Late Ordovician up to the Late Jurassic. The grade of the orogenic dynamo-thermal metamorphism varies from the late diagenetic zone through the anchizone up to the epizone (chlorite, maximally biotite isograd of the greenschist facies). The K-Ar system of the illite-muscovite in the < 2 m grain-size fraction approached equilibrium only in epizonal and high-temperature anchizonal conditions. The orogenic metamorphism culminated between the eo-Hellenic (160-120 Ma) phase connected to the beginning of the subduction in the Dinarides, and the Austrian (100-95 Ma) phase characterized by compressional crustal thickening. No isotope geochronological evidence was found for proving any Hercynian recrystallization. The stability field of fission tracks in zircon was approached using the thermal histories of the different tectonic units. A temperature less than 250°C and effective heating time of 20–30 Ma had only negligible effects on the tracks, whereas total annealing was reached between 250 and 300°C. Apatite fission track ages from the Paleozoic and Mesozoic formations show that the uplift of the Bükk Mountains occurred only in the Tertiary (not earlier than ca. 40 Ma ago). Thermal modeling based on apatite fission track length spectra and preserved Paleogene sediment thickness data proved that the Late Neogene burial of the recently exhumed plateau of the Bükk Mountains exceeded 1 km. 相似文献
16.
The Amur and Kiselevka–Manoma accretionary complexes belong to the Cretaceous Khingan–Okhotsk active continental margin, which was formed in the east of Eurasia as a result of the subduction of the Pacific oceanic plates. The Kiselevka–Manoma complex is composed of oceanic pelagic and hemipelagic sedimentary rocks and intraplate oceanic basalts. It is located to the southeast, along the ocean-faced front of the Amur complex, which is predominantly composed of turbidites of the convergent boundary of lithospheric plates. The biostratigraphic study of radiolarians from rocks of the frontal part of the Amur complex allowed us to correlate them with rocks of the Kiselevka–Manoma complex and to define the period of accretion to be from the Late Aptian to the Middle Albian. The tectonostratigraphic interrelations of these two contrasting lithotectonic complexes are established and two possible models of their common emplacement are suggested. Both models suppose a continuous spatiotemporal relation of complexes with the primary paleolocation of the Kiselevka–Manoma complex in front of (on the ocean side) the Amur complex. The frontal part of the Amur complex and the Kiselevka–Manoma complex were emplaced synchronously with the western part of the East Sakhalin accretionary complex. This scenario defines the Early Cretaceous tectonic zonation of the region and the choice of the appropriate paleotectonic model. At the end of the Early Cretaceous, a single convergent boundary of the lithospheric plates is suggested with the position of the Sakhalin island arc system south of the Khingan–Okhotsk active continental margin. 相似文献
17.
Markus Egli 《GeoJournal》1998,44(1):73-89
Data on element fluxes (Ca, K, N) are presented which were obtained in the course of an extended project on element-cycling in a forested ecosystem near Möhlin, northwestern Switzerland. Current fluxes of Ca, K, and N could be compared with historical fluxes (1969–1993) with the help of soil chemistry inventories since 1969, data on the forest management, and atmospheric deposition. Since 1969, soil chemistry has significantly changed due to a distinct disintegration of humus. The decomposition of organic matter influenced strongly the element cycling. Due to this mineralization high amounts of N were released. It is, however, not fully clear in which chemical form N has been transferred out of the system. Two possible hypotheses on the N losses are defined. According to the calculated proton budget and measured element changes in the soil, it is hypothized that a large part of the mineralized organic N presumably was transformed into N2 or more likely into N2O. A complete nitrification of organically bound N to NO3
– is also discussed but is, however, considered as less probable. In contrast to K, Ca proved to be a very sensitive element: the exchangeable Ca stock has been decreased sharply. The analysis of the current fluxes of Ca, K, and N reveals that nitrogen is abundantly present in the forest system with the consequence that the ecological balance is shifted in favour of N. Accordingly, the supply of base cations is rather scarce for the plants. Furthermore, the influence of forest management on element fluxes seems to be substantial, especially on the fluxes of base cations, but can be reduced with simple measures (e.g. removal of the bark of coniferous trees). 相似文献
18.
Baumgartner and Rumble (1988) apply a kinetic continuum theory for stable isotope transport to unidimensional infiltration of fluid into rock. Their numerical applications are restricted to the simplified case of rapid isotope exchange between phases, where the sharp isotope fronts of pure advection are distended by dispersive mechanisms only. However, kinetic limitations of isotope exchange are potentially an equally important distending mechanism, and it will only rarely be possible to ascribe front gradients to diffusion/dispersion alone. Abrupt isotopic changes at vein boundaries are more often a secondary signal of lithologic change than the expression of a retarded advective front. At such boundaries, diffusion and dispersion play a role that is comparable to, or greater than, that of advection, so that the detailed shapes of isotope fronts depend upon boundary conditions for the infiltration process. Zerodimensional box models have legitimate, if limited, uses in the modelling of fluid-rock interaction, and are reexamined. 相似文献
19.
İbrahim Uysal Mahmud Tarkian M. Burhan Sadiklar Federica Zaccarini Thomas Meisel Giorgio Garuti Stefanie Heidrich 《Contributions to Mineralogy and Petrology》2009,158(5):659-674
Ultramafic rocks around the city of Muğla in SW Turkey are represented by mantle peridotites depleted to various degrees,
ranging from cpx-rich harzburgites to depleted harzburgite and dunite. Cpx-rich harzburgites are thought to be the residua
left after extraction of MORB-type basalt, from which high-Al chromitite [49.2 < Cr# = 100 × Cr/(Cr + Al) < 53.5] crystallised
with a higher proportion of 187Os/188Os (average of 0.1361). However, depleted harzburgites are assumed to be the residua left after extraction of hydrous boninitic
melt produced by second stage partial melting of already depleted mantle due to a subducting slab, from which high-Cr chromitites
(64.2 < Cr# < 85.9) with lower and heterogeneous 187Os/188Os ratio (average of 0.1324) were crystallised as a result of melt–rock interaction in a supra-subduction environment. Dunites
around the chromite deposits are considered to be the product of melt–peridotite interaction. Most of the chromitites contain
high-Cr chromite and display enrichment in IPGE (Os, Ir, Ru) over PPGE (Rh, Pt, Pd), with PGE concentrations between 61 and
1,305 ppb. Consistently, laurite-erlichmanite series minerals with various Os concentrations are found to be the most abundant
PGM inclusions in chromite. Os–Ir–Ru alloy, irarsite, and kashinite, as well as Pt–Fe alloy and Pt-oxide, which are not common
in ophiolitic chromitites, were also detected as magmatic PGM inclusions. Pentlandite, millerite, and, rarely heazlewoodite
form the magmatic inclusions of base-metal sulphide. The presence of olivine and clinopyroxene, as well as hydrous silicate
inclusions such as amphibole and phlogopite, in high-Cr chromitite supports the idea that high-Cr chromitites were formed
in a supra-subduction environment. 相似文献
20.
The barium deposits in Ankang and Xunyang counties,Shaanxi Province,China,occur in the northernmost part of the world-class barium metallogenic belt in south Qinling.The deposits are hosted by the Lower Silurian carbonaceous siliceous rocks,with a unique combination of barite and witherite.The homogenization temperatures of fluid inclusions in the barite are mainly concentrated between 135 and 155 ℃,whereas those from the witherite have two peaks of 165-175 ℃,and 215-225℃,respectively.Laser Raman analysis of fluid inclusions indicates that the vapor phase of fluid inclusions in barite is dominated by H_2O,although some contains N_2,H_2S,and CH_4.The compositions of the vapor and liquid phases of fluid inclusions in witherite can be divided into two end-members,one dominated by H_2O without other volatiles,and the other containing CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6 in addition to H_2O.CO_2,H_2S,and some CH_4 are interpreted as products of chemical reactions during mineralization.Organic gases(CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6) in the fluids were critical in the formation of barium sulfate versus carbonate.The δ~(34)S values of barite range from 38.26‰ to54.23‰(CDT),the δ~(34)S values of sulfides coexisting with barium minerals vary from 22.44‰ to25.11‰(CDT),and those in the wall rock from 11.60‰ to 19.06‰(CDT).We propose that the SO_4~(2-)generally experienced bacterial sulfate reduction in seawater before mineralization,and some SO_4~(2-)also experienced thermochemical sulfate reduction in hydrothermal system during mineralization.The δ~(13)C values of witherite range from-27.30‰ to-11.80‰(PDB),suggesting that carbon was sourced from organic substances(like CH_4,C_2H_4,and C_2H_6).The formation of witherite was possibly associated with thermochemical sulfate reduction,which caused the consumption of the organic gases and SO_4~(2-) in the hydrothermal solutions,consequently inhibiting barite formation.The important conditions for forming witherite include high fluid temperatures,high Ba~(2+) concentrations,CO_2 in the fluids,low HS~- concentrations,and the subsequent rapid diffusion of H_2S during thermochemical sulfate reduction of the fluids. 相似文献