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1.
A gas condensate from well ND1 in the Jizhong Depression of the Bohai Bay Basin, China is characterized by two-dimensional gas chromatography with flame ionization detector (GC × GC–FID) and time-of-flight mass spectrometry (GC × GC–TOFMS). This condensate is sourced from the fourth member of the Shahejie Formation (Es4) but reservoired in the Mesoproterozoic Wumishan Formation carbonate at a depth of 5641–6027 m and the reservoir temperature is 190–201 °C. It is the deepest and the highest temperature discovery in the basin to date. The API gravity of the condensate is 51° and the sulfur content is < 0.04%. A total of 4955 compounds were detected and quantified. Saturated hydrocarbons, aromatic hydrocarbons and non-hydrocarbon account for 94.8%, 5.1% and 0.02% of the condensate mass, respectively. Some long chain alkylated cyclic alkanes, decahydronaphthalenes and diamondoids are tentatively identified in this condensate. The C6–C9 light hydrocarbon parameters show that the gas condensate was generated at relatively high maturity but its generation temperature derived from the dimethylpentane isomer ratio seems far lower than the current reservoir temperature. Some light hydrocarbon parameters indicate evaporative fractionation may also be involved due to multiple-charging and mixing. The diamondoid concentrations and gas oil ratio (GOR) suggest that the ND1 condensate results from 53.3–55% cracking. Since significant liquids remain, the exploration potential of ultra-deep buried hill fields in the Bohai Bay Basin remains high. 相似文献
2.
Six monoterpenoid hydrocarbons including two acyclic, two monocyclic and two aromatic components were identified and quantified in 49 oil and condensate samples using comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC × GC–TOFMS). Among them, 2,6-dimethyloctane (2,6-DMO) and 2-methyl-3-ethylheptane (2-M-3-EH) are the most abundant compounds and geochemically significant. Used in conjunction with other geochemical parameters such as pristane/phytane (Pr/Ph) and dibenzothiophene/phenanthrene (DBT/P) ratios, the 2-M-3-EH/2,6-DMO ratio (monoterpane ratio, MTR) provides a useful tool for distinguishing marine oils and condensates from those of terrigenous origin. Oils and condensates derived from marine source rocks have high MTR (> 0.4), low Pr/Ph and high DBT/P values, whereas those generated from terrigenous source rocks have lower MTR (< 0.3), higher Pr/Ph and lower DBT/P values. Differences in MTR values are mainly caused by variations in the concentrations of 2-M-3-EH as the concentrations of 2,6-DMO are in the same range in different sample groups. The 2-M-3-EH is enriched in marine oils and condensates from highly anoxic depositional environments, but depleted in terrigenous oils and condensates from oxic/sub-oxic depositional environments. The MTR may serve as a new parameter for assigning the source rock depositional environment. MTR values higher than 0.4 may indicate reducing conditions while MTR values lower than 0.3 may suggest an oxic/sub-oxic condition. 相似文献
3.
Modern seafloor hydrothermal systems provide important insights into the formation and discovery of ancient volcanic-hosted massive sulfide (VHMS) deposits. In 2010, Integrated Ocean Drilling Program (IODP) Expedition 331 drilled five sites in the Iheya North hydrothermal field in the middle Okinawa Trough back-arc basin, Japan. Hydrothermal alteration and sulfide mineralization is hosted in a geologically complex, mixed sequence of coarse pumiceous volcaniclastic and fine hemipelagic sediments, overlying a dacitic to rhyolitic volcanic substrate. At site C0016, located adjacent to the foot of the actively venting North Big Chimney massive sulfide mound, massive sphalerite-(pyrite-chalcopyrite ± galena)-rich sulfides were intersected (to 30.2% Zn, 12.3% Pb, 2.68% Cu, 33.1 ppm Ag and 0.07 ppm Au) that strongly resemble the black ore of the Miocene-age Kuroko deposits of Japan. Sulfide mineralization shows clear evidence of formation through a combination of surface detrital and subsurface chemical processes, with at least some sphalerite precipitating into void space in the rock. Volcanic rocks beneath massive sulfides exhibit quartz-muscovite/illite and quartz-Mg-chlorite alteration reminiscent of VHMS proximal footwall alteration associated with Kuroko-type deposits, characterized by increasing MgO, Fe/Zn and Cu/Zn with depth. Recovered felsic footwall rocks are of FII to FIII affinity with well-developed negative Eu anomalies, consistent with VHMS-hosting felsic rocks in Phanerozoic ensialic arc/back-arc settings worldwide.Site C0013, ∼100 m east of North Big Chimney, represents a likely location of recent high temperature discharge, preserved as surficial coarse-grained sulfidic sediments (43.2% Zn, 4.4% Pb, 5.4% Cu, 42 ppm Ag and 0.02 ppm Au) containing high concentrations of As, Cd, Mo, Sb, and W. Near surface hydrothermal alteration is dominated by kaolinite and muscovite with locally abundant native sulfur, indicative of acidic hydrothermal fluids. Alteration grades to Mg-chlorite dominated assemblages at depths of >5 mbsf (metres below sea floor). Late coarse-grained anhydrite veining overprints earlier alteration and is interpreted to have precipitated from down welling seawater as hydrothermal activity waned. At site C0014, ∼350 m farther east, hydrothermal assemblages are characterized by illite/montmorillonite, with Mg-chlorite present at depths below ∼30 mbsf. Recovered lithologies from distal, recharge site C0017 are unaltered, with low MgO, Fe2O3 and base metal concentrations.Mineralization and alteration assemblages are consistent with the Iheya North system representing a modern analogue for Kuroko-type VHMS mineralization. Fluid flow is focussed laterally along pumiceous volcaniclastic strata (compartmentalized between impermeable hemipelagic sediments), and vertically along faults. The abundance of Fe-poor sphalerite and Mg-rich chlorite (clinochlore/penninite) is consistent with the lower Fe budget, temperature and higher oxidation state of felsic volcanic-hosted hydrothermal systems worldwide compared to Mid Ocean Ridge black smoker systems. 相似文献
4.
In this paper, we present U–Pb ages and trace element compositions of titanite from the Ruanjiawan W–Cu–Mo skarn deposit in the Daye district, eastern China to constrain the magmatic and hydrothermal history in this deposit and provide a better understanding of the U–Pb geochronology and trace element geochemistry of titanite that have been subjected to post-crystallization hydrothermal alteration. Titanite from the mineralized skarn, the ore-related quartz diorite stock, and a diabase dike intruding this stock were analyzed using laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). Titanite grains from the quartz diorite and diabase dike typically coexist with hydrothermal minerals such as epidote, sericite, chlorite, pyrite, and calcite, and display irregular or patchy zoning. These grains have low LREE/HREE and high Th/U and Lu/Hf ratios, coupled with negative Eu and positive Ce anomalies. The textural and compositional data indicate that titanite from the quartz diorite has been overprinted by hydrothermal fluids after being crystallized from magmas. Titanite grains from the mineralized skarn are texturally equilibrated with retrograde skarn minerals including actinolite, quartz, calcite, and epidote, demonstrating that these grains were formed directly from hydrothermal fluids responsible for the mineralization. Compared to the varieties from the quartz diorite stock and diabase dike, titanite grains from the mineralized skarn have much lower REE contents and LREE/HREE, Th/U, and Lu/Hf ratios. They have a weighted mean 206Pb/238U age of 142 ± 2 Ma (MSWD = 0.7, 2σ), in agreement with a zircon U–Pb age of 144 ± 1 Ma (MSWD = 0.3, 2σ) of the quartz diorite and thus interpreted as formation age of the Ruanjiawan W–Cu–Mo deposit. Titanite grains from the ore-related quartz diorite have a concordant U–Pb age of 132 ± 2 Ma (MSWD = 0.5, 2σ), which is 10–12 Ma younger than the zircon U–Pb age of the same sample and thus interpreted as the time of a hydrothermal overprint after their crystallization. This hydrothermal overprint was most likely related to the emplacement of the diabase dike that has a zircon U–Pb age of 133 ± 1 Ma and a titanite U–Pb age of 131 ± 2 Ma. The geochronological results thus reveal two hydrothermal events in the Ruanjiawan deposit: an early one forming the Wu–Cu–Mo ores related to the emplacement of the quartz diorite stock and a later one causing alteration of the quartz diorite and its titanite due to emplacement of diabase dike. It is suggested that titanite is much more susceptible to hydrothermal alteration than zircon. Results from this study also highlight the utilization of trace element compositions in discriminating titanite of magmatic and hydrothermal origins, facilitating a more reasonable interpretation of the titanite U–Pb ages. 相似文献
5.
This report describes in situ ion microprobe U–Pb dating of a protoconodont, an early Cambrian phosphate microfossil, using laterally high-resolution secondary ion mass spectrometry (NanoSIMS). On a single fragment of a fossil (approximately 850 μm × 250 μm) derived from a sedimentary layer in the Meishucunian Yuhucun Formation, Yunnan Province, southern China, 23 spots provide a 238U/206Pb isochron age of 547 ± 43 Ma (2σ, MSWD = 1.9), which is consistent with the depositional age, 536.5 ± 2.5 Ma estimated using zircon U–Pb dating of interbedded tuffs. However, five spots on a small region (approximately 250 μm × 100 μm) in the same protoconodont yield an isochron age of 417 ± 74 Ma (2σ, MSWD = 0.31), apparently younger than the formation age. The younger age might be attributable to a later hydrothermal event, perhaps associated with Caledonian orogenic activity recorded in younger zircon with an age of 420–440 Ma. We also measured 87Sr/86Sr ratios of the protoconodont by NanoSIMS. In the older domain, 19 spots give the 87Sr/86Sr ratio of 0.71032 ± 0.00023 (2σ), although seven spots on the younger region provide the ratio of 0.70862 ± 0.00045; this is significantly less radiogenic than the older domain. This is the first report of U–Pb age and Sr isotope heterogeneity within a single fragment of micro-fossil (215). 相似文献
6.
《Applied Geochemistry》2002,17(11):1467-1494
Samples from the Ocean Drilling Program Leg 169 in Escanaba Trough, Gorda Ridge, NE Pacific Ocean, were analyzed to study maturation by accelerated diagenesis and/or by catagenesis of the sedimentary organic matter to hydrothermal petroleum. At Site 1038 the hydrothermal petroleums have migrated after generation to shallower horizons. The n-alkane maturation was indicated by the strong even C number preference (i.e., CPI <1.0) as in the case of Middle Valley. All samples contained admixed organic matter of terrigenous and marine components as indicated by the distributions of the biomarkers. The biological precursors were catagenetically altered to their equivalent mature compounds. The presence of high molecular weight PAHs in some sediment sections at Site 1038 reflected the high temperature alteration and reworking of organic matter into mature hydrothermal petroleum. At Site 1037, the reference hole in the Escanaba Trough, the n-alkanes with a strong predominance of odd C number homologs reflected immature non-marine lipid components essentially throughout the hole. Maturation of organic matter was only observed below 450 mbsf with n-alkanes showing a CPI <1.0. The strong even C number predominance in those intervals was attributed to initial maturation by high heat flow during the early rifting process. 相似文献
7.
The Mn-Ba-Pb deposit at Aspro Gialoudi in NW Milos is shown to be a fossil inhalative-exhalative hydrothermal deposit that represents the deepest part of the Vani succession at the western extremity of the main Vani manganese deposit. The geology of the Vani-Aspro Gialoudi area is characterized by Upper Pliocene-Lower Pleistocene dacitic and rhyodacitic lava domes, which are overlain by the Vani volcaniclastic unit considered to be part of the 2.66–1.44 Ma magmatic event at Milos Island. The presence of in-situ and intrusive hyaloclastite breccias surrounding the coherent lava domes at Aspro Gialoudi and Vani areas indicates submarine emplacement for the domes. The dacitic-rhyodacitic domes are variously altered (mainly propylitic and/or argillic alteration, silicified and in some cases locally exhibiting adularia alteration). Both Aspro Gialoudi and main Vani deposit are located proximal to fault systems: the main Vani manganese deposit is adjacent to the NW-trending Kondaros-Katsimouti-Vani Dome fault, whereas the Aspro Gialoudi deposit is adjacent to the relatively minor NE-trending fault on the west coast of Milos. At Aspro Gialoudi, mineralization took place in a subseafloor and/or seafloor environment and is characterized by a stratabound Mn-barite-rich deposit mainly within a package of propylitized intrusive hyaloclastites and within the overlying sandstones. Banded epithermal veins trending NE-SW and composed of chalcedonic silica/quartz + barite + Mn-oxide ± sulfides crosscut the dacitic lavas, the hyaloclastites and the overlying volcaniclastic sequence at Aspro Gialoudi and are considered to represent the feeder zones of the manganese-barite mineralization. Within the veins, early sulfide (galena-sphalerite) barite and quartz deposition is followed by manganese oxides and aragonite, thus resembling the epithermal-style Pb-Zn-Ag-Mn mineralization across the NW-trending Katsimoutis-Kondaros-Vani fault. Mineralization in Aspro Gialoudi and Vani deposits seems to be controlled by alternating cycles of deposition of sulfides and hydrothermal manganese oxides within the faults. Manganese deposition in both deposits formed in a similar manner, namely by transport of hydrothermal fluids through the adjacent fault systems into a reservoir of volcanoclastic sandstone and hyaloclastites to produce a deposit initially consisting of principally of pyrolusite and occasionally ramsdellite, which were subsequently replaced by cryptomelane, hollandite, coronadite and hydrohaeterolite. Precipitation of hydrothermal manganese oxides took place very quick and under microbial Mn(II) oxidation. Compositional data show that metallic elements most enriched in the Aspro Gialoudi and Vani manganese deposits relative to the average continental crust, lie in the sequences Pb > Cd > Mn > As > Sb > Zn > W > Tl > Ba > Cu > Mo > Co > Bi and As > Sb > Pb > Mn > Tl > Cd > Zn > W > Cu > Ba > Mo > Co, respectively. Mineralogical and geochemical (e.g. REE) data from both Aspro Gialoudi and main Vani deposit are taken to indicate mainly a seawater source for the hydrothermal fluids. These two deposits are genetically and spatially related to base- and precious metal intermediate-sulfidation epithermal mineralization. They formed successively by similar processes and are considered to be integral parts of the same hydrothermal system. 相似文献
8.
This study investigated Holocene and fossil hydrothermal manganese deposits in the Izu-Ogasawara arc. Mineralogically, these deposits comprise 10 Å and 7 Å manganate minerals, and the fossil samples showed higher 10 Å stabilities. Chemical compositions of the Holocene samples are typical of other hydrothermal manganese deposits, including low Fe/Mn ratios, low trace metals, and low rare earth elements. Although the fossil samples generally have similar chemical characteristics, they exhibit significant enrichment in Ni, Cu, Zn, Cd, Ba, REE, Tl, and Pb contents. Furthermore, the chondrite-normalized REE patterns showed more light REE enrichment trends. These chemical characteristics suggest post-depositional uptake of these metals from seawater. U-Th dating of a Holocene hydrothermal manganese deposit from the Kaikata Seamount indicated 8.8 ± 0.94 ka for the uppermost layer and downward growth beneath the seafloor with a growth rate of ca. 2 mm/kyr. This is approximately three orders of magnitude faster than that of hydrogenetic ferromanganese crusts. U-Pb age of a fossil hydrothermal manganese deposit from the Nishi-Jokyo Seamount showed 4.4 ± 1.6 Ma, which was contemporary with basaltic volcanism (5.8 ± 0.3 Ma). Hydrothermal manganese deposits contain high concentrations of high value Mn, but only small amounts of valuable minor metals; their ages constrain the periods of past hydrothermal activity and provide a vector to explore for polymetallic sulfide deposits. 相似文献
9.
Although the effects of biodegradation on the composition and physical properties of crude oil have been well studied, effects of in-reservoir petroleum biodegradation on molecular and isotopic compositions of crude oils are not yet clearly understood. The Alberta Basin, in western Canada, is one of the world’s largest petroleum accumulations and constitutes an ideal example of a natural suite of sequentially biodegraded oils. The basin hosts moderately to severely biodegraded petroleum, regionally distributed and in single, more or less continuous, oil columns. In this study, a series of oil samples from the Alberta heavy oil and oil sands provinces, with varying degrees of biodegradation, were analyzed to assess the impact of progressive biodegradation on the molecular and C, H, N, and S isotopic compositions of oils. The results of the molecular characterization of the hydrocarbon fraction of the studied oils show that the oils have suffered biodegradation levels from 2 to 10+ (toward the Alberta–Saskatchewan border) on the Peters and Moldowan scale of biodegradation (abbreviated PM 2 to PM 10) and from tens to hundreds on the Manco scale. Within single reservoirs, increasing biodegradation was observed from top to bottom of the oil columns at all sites studied. The whole oil stable isotopic compositions of the samples varied in the ranges δ13C = −31.2‰ to −29.0‰, δ2H = −147‰ to −133‰, δ15N = 0.3–4.7‰ and δ34S = 0.4–6.4‰. The maximum differences between δ values of samples (Δ) within single oil columns were Δ13C = 1.4‰, Δ2H = 7‰, Δ15N = 1.7‰ and Δ34S = 1.0‰. Regional variations in the isotopic compositions of oil samples from different wells (averaged values from top to bottom) were 1.2‰ for δ13C, 12‰ for δ2H, 4.1‰ for δ15N and 5.5‰ for δ34S and hence generally significantly larger variations were seen than variations observed within single oil columns, especially for N and S. It appears that even severe levels of biodegradation do not cause observable systematic variations in carbon, nitrogen or sulfur isotope composition of whole oils. This indicates that sulfur and nitrogen isotopic compositions may be used in very degraded oils as indicators for oil charge from different source rock facies. 相似文献
10.
Uranium(VI) sorption onto kaolinite was investigated as a function of pH (3–12), sorbate/sorbent ratio (1 × 10?6–1 × 10?4 M U(VI) with 2 g/L kaolinite), ionic strength (0.001–0.1 M NaNO3), and pCO2 (0–5%) in the presence or absence of 1 × 10?2–1 × 10?4 M citric acid, 1 × 10?2–1 × 10?4 M EDTA, and 10 or 20 mg/L fulvic acid. Control experiments without-solids, containing 1 × 10?6–1 × 10?4 M U(VI) in 0.01 M NaNO3 were used to evaluate sorption to the container wall and precipitation of U phases as a function of pH. Control experiments demonstrate significant loss (up to 100%) of U from solution. Although some loss, particularly in 1 × 10?5 and 1 × 10?4 M U experiments, is expected due to precipitation of schoepite, adsorption on the container walls is significant, particularly in 1 × 10?6 M U experiments. In the absence of ligands, U(VI) sorption on kaolinite increases from pH ～3 to 7 and decreases from pH ～7.5 to 12. Increasing ionic strength from 0.001 to 0.1 M produces only a slight decrease in U(VI) sorption at pH < 7, whereas 10% pCO2 greatly diminishes U(VI) sorption between pH ～5.5 and 11. Addition of fulvic acid produces a small increase in U(VI) sorption at pH < 5; in contrast, between pH 5 and 10 fulvic acid, citric acid, and EDTA all decrease U(VI) sorption. This suggests that fulvic acid enhances U(VI) sorption slightly via formation of ternary ligand bridges at low pH, whereas EDTA and citric acid do not form ternary surface complexes with the U(VI), and that all three ligands, as well as carbonate, form aqueous uranyl complexes that keep U(VI) in solution at higher pH. 相似文献
11.
The study presents copper (Cu) isotope data of mineral separates of chalcopyrite from four drill core samples in the Miocene Dabu porphyry Cu-Mo deposit formed in a post-collisional setting in the Gangdese porphyry copper belt, southern Tibet. Copper isotope values in hypogene chalcopyrite range from –1.48‰ to +1.12‰, displaying a large variation of up to 2.60‰, which demonstrates Cu isotope fractionation at high-temperature during hydrothermal evolution. The majority of measured chalcopyrite isotopic compositions show a gradual increasing trend from –1.48‰ to +1.12‰ with the increase of drilling depth from 130m to 483m, as the alteration assemblages change from potassic to phyllic. Similarly, the other δ65Cu values (δ65Cu = ((65Cu/63Cu)sample/(65Cu/63Cu)standard − 1) × 1000) of the chalcopyrite show a gradual increasing trend from −1.48‰ to +0.59‰ with the decrease of drilling depth from 130 m to 57 m, as the alteration assemblages change from potassic, phyllic, through argillic to relatively fresh. These observations suggest a genetic link between Cu isotope variation and silicate alteration assemblages formed at different temperatures, indicative of a Rayleigh precipitation process resulting in the large variation of δ65Cu values at Dabu. In general, samples closest to the center of hydrothermal system dominated by high-temperature potassic alteration are isotopically lighter, whereas samples dominated by low-temperature phyllic alteration peripheral to the center are isotopically heavier. The predicted flow pathways of hydrothermal fluids are from No. 0 to No. 3 exploration line, and the lightest δ65Cu values are the most proximal to the hydrothermal source. Finally, we propose that the northwest side of the No. 0 exploration line has high potential for hosting undiscovered orebodies. The pattern of Cu isotope variation in conjunction with the features of silicate alteration in porphyry system can be used to trace the hydrothermal flow direction and to guide mineral exploration. 相似文献
12.
《Applied Geochemistry》2003,18(6):845-861
Recent sediments of the Andaman Backarc Basin, Indian Ocean, between the Andaman Nicobar islands and the Malay Peninsula have been analyzed for biomarker lipids. Three cores were selected: one each from the fault zone in a deep basin (a graben between two fault systems), another from a location adjacent to the fault, and the third from the topographic high in the rift valley. The molecular composition of the lipid classes (n-alkanes, isoprenoids, alkylbenzenes, alkylcyclohexanes, hopanoids, polycyclic aromatic hydrocarbons, steranes, alcohols, sterols and fatty acids) was examined by gas chromatography (GC) and GC/mass spectrometry to understand the nature and source of the hydrocarbons present and the processes of maturation of organic matter. The data show that the hydrocarbons are of hydrothermal origin, derived from thermal alteration of sedimentary organic matter, consisting of a mixture predominantly of marine-derived components with some terrestrial inputs. Normal alcohols and fatty acids also corroborate the distribution of n-alkanes. The distribution profiles and various parameters computed from the concentration of the target compounds suggest that oxidative reactions and microbial degradation in this environment are insignificant. Triterpane and PAH compositions indicate that the thermal maturity of the bitumen in the samples is comparable to or lower than that found at other hydrothermal regions such as the Northern Juan de Fuca Ridge, Guaymas Basin and Escanaba Trough. 相似文献
13.
The large, newly discovered Sharang porphyry Mo deposit and nearby Yaguila skarn Pb–Zn–Ag (–Mo) deposit reside in the central Lhasa terrane, northern Gangdese metallogenic belt, Tibet. Multiple mineral chronometers (zircon U–Pb, sericite 40Ar–39Ar, and zircon and apatite (U–Th)/He) reveal that ore-forming porphyritic intrusions experienced rapid cooling (> 100 °C/Ma) during a monotonic magmatic–hydrothermal evolution. The magmatic–hydrothermal ore-forming event at Sharang lasted ~ 6.0 Myr (~ 1.8 Myr for cooling from > 900 to 350 °C and ~ 4.0 Myr for cooling from 350 to 200 °C) whereas cooling was more prolonged during ore formation at Yaguila (~ 1.8 Myr from > 900 to 500 °C and a maximum of ~ 16 Myr from > 900 to 350 °C). All porphyritic intrusions in the ore district experienced exhumation at a rate of 0.07–0.09 mm/yr (apatite He ages between ~ 37 and 30 Ma). Combined with previous studies, this work implies that uplift of the eastern section of the Lhasa terrane expanded from central Lhasa (37–30 Ma) to southern Lhasa (15–12 Ma) at an increasing exhumation rate. All available geochronologic data reveal that magmatic–hydrothermal–exhumation activities in the Sharang–Yaguila ore district occurred within four periods of magmatism with related mineralization. Significant porphyry-type Mo mineralization was associated with Late Cretaceous–Eocene felsic porphyritic intrusions in the central Lhasa terrane, resulting from Neotethyan oceanic subduction and India–Asia continental collision. 相似文献
14.
Studies of sulfur and lead isotopic compositions in hydrothermal deposits are an important tool to determine the source and processes of both sulfur and lead, and to understand the origin of hydrothermal ore deposits. Here, the sulfur and lead isotopic compositions of sulfide minerals have been studied for different hydrothermal fields in the East Pacific Rise (EPR), Mid-Atlantic Ridge (MAR), Central Indian Ridge (CIR), Southwest Indian Ridge (SWIR), and North Fiji Basin (NFB). The sulfur isotopic compositions of the studied sulfide samples are variable (δ34S 0.0 to 9.6‰, avg. δ34S 4.7‰; n = 60), being close to the associated igneous rocks (~ 0‰ for, e.g., basalt, serpentinized peridotite), which may reflect the S in the sulfide samples is derived mainly from the associated igneous rocks, and a relatively small proportion (< 36%) of seawater sulfur incorporated into these sulfides during mixing between seawater (δ34S 21‰) and hydrothermal fluid. In contrast for a mixed origin for the source of S, the majority of the lead isotopic compositions (206Pb/204Pb 17.541 ± 0.004 to 19.268 ± 0.001, 207Pb/204Pb 15.451 ± 0.001 to 15.684 ± 0.001, 208Pb/204Pb 37.557 ± 0.008 to 38.988 ± 0.002, n = 21) of the sulfides possess a basaltic Pb isotopic composition, suggesting that the lead in the massive sulfide is mainly leached from local basaltic rocks that host the sub-seafloor hydrothermal systems in sediment-free mid-ocean ridges and mature back-arc basins. Furthermore, sulfide minerals in the super-fast and fast spreading mid-ocean ridges (MORs) exhibit less spread in their the δ34S values compared to sulfides from super-slow, and slow spreading MORs, which is most easily explained as a lesser degree of fluid-rock interaction and hydrothermal fluid-seawater mixing during hydrothermal ore-forming process. Additionally, the S and Pb isotope compositions of sulfides are controlled by the fluid processes for forming seafloor massive sulfide deposits. We demonstrate that the variable sulfur and lead isotopic compositions exhibit a relationship with the sulfur and lead sources, fluid–rock interaction, and fluid–seawater mixing. 相似文献
15.
The Dalucao deposit, located in western Sichuan Province, southwestern China, in the western part of the Yangtze Craton, is one of the largest and most extensive rare earth element (REE) deposits in the Himalayan Mianning–Dechang REE belt. Moreover, the Dalucao deposit is the only deposit identified in the southern part of the belt. The Dalucao deposit contains the No. 1, 2, and 3 orebodies; the No. 1 and 3 orebodies are both hosted in two breccia pipes, located in syenite–carbonatite host rocks. Both pipes have elliptical cross-sections at the surface, with long-axis diameters of 200–400 m and short-axis diameters of 180–200 m; the pipes extend downwards for > 450 m. No. 1 and No. 3 have total thickness varying between 55 and 175 m and 14 to 58 m respectively. The REE mineralization is associated with four brecciation events, which are recorded in each of the pipes. The ore grades in the No. 1 and 3 orebodies are similar, and consist of 1.0%–4.5% rare earth oxides (REOs). The No. 1 orebody is characterized by a Type I mineral assemblage (fluorite + barite + celestite + bastnäsite), whereas the No. 3 orebody is characterized by a Type II assemblage (fluorite + celestite + pyrite + muscovite + bastnäsite + strontianite). Argon (40Ar/39Ar) dating of hydrothermal muscovite intergrown with REE minerals in typical ores from the No. 1 and 3 orebodies yielded similar ages of 12.69 ± 0.13 and 12.23 ± 0.21 Ma, respectively, which suggest that both mineral assemblages formed coevally, rather than in paragenetic stages. Both ages are also similar to the timing of intrusion of the syenite–carbonatite complex (12.13 ± 0.19 Ma). The ore-mineral assemblages occur in breccias, veinlets, and in narrow veins. The ore veinlets, which usually show a transition to mineralized breccia or brecciated ores, are commonly enveloped by narrow veins and stringer zones with comparable mineral assemblages. The brecciated ores form 95% of the volume of the deposit, whereas brecciated ores are only a minor constituent of other deposits in the Mianning–Dechang REE belt. The carbonatite in the syenite–carbonatite complexes contains high concentrations of S (0.07–2.32 wt.%), Sr (16,500–20,700 ppm), Ba (3600–8400 ppm), and light REEs (LREE) (2848–10,768 ppm), but is depleted in high-field-strength elements (HFSE) (Nb, Ta, P, Zr, Hf, and Ti). The syenite is moderately enriched in large-ion lithophile elements (LILE), Sr (155–277 ppm), and Ba (440–755 ppm). The mineralized, altered, and fresh syenites and carbonatites exhibit similar trace element compositions and REE patterns. Brecciation events, and the Dalucao Fault and its secondary faults around the deposit, contributed to the REE mineralization by facilitating the circulation of ore-forming fluids and providing space for REE precipitation. Some hydrothermal veins composed of coarse-grained fluorite and quartz are distributed in the syenite–carbonatite complex. The oxygen isotope compositions of ore-forming fluids in equilibrium with quartz at 215 °C are − 4.95‰ to − 7.45‰, and the hydrogen isotope compositions of fluid inclusions in coarse-grained quartz are − 88.4‰ to − 105.1‰. The syenite–carbonatite complex and carbonatite are main contributors to the mineralization in the geological occurrence. Thus, the main components of the ore-forming fluids were magmatic water, meteoric water, and CO2 derived from the decarbonation of carbonatite. According to the petrographic studies, bastnäsite mineralization developed during later stages of hydrothermal evolution and overprinted the formation of the brecciated fluorite–quartz hydrothermal veins. As low-temperature isotope exchange between carbonates of the carbonatite and water-rich magmatic fluids will lead to positive shifts in δ18O values of the carbonates, C–O isotopic compositions from the bulk primary carbonatite to hydrothermal calcite and bastnäsite changed (δ18OV-SMOW from 8.0‰ to 11.6‰, and δ13C V-PDB from − 6.1 to − 8.7‰). According to the chemical composition of syenite and carbonatite, REE chloride species are the primary complexes for the transport of the REEs in the hydrothermal fluids, and the presence of bastnäsite and parisite means the REE were precipitated as fluorocarbonates. High contents of Sr, Ba and S in the syenite–carbonatite complex led to the deposition of large amount of barite and celestite. 相似文献
16.
The Hongtoushan volcanogenic massive sulfide (VMS) deposit is the largest Archean Cu–Zn deposit in China, located in the Qingyuan greenstone belt on the northern margin of the North China Craton. The Cu–Zn mineralization was stratigraphically controlled by the interbeds (~ 100 m in thickness) of mafic–felsic volcanic sets and overlain by banded iron layers. However, the relationship between VMS deposits and associated volcanics has not been examined. This study ultimately clarifies the times and sources of the volcanics and mineralization. Based on in situ zircon U–Pb and O isotope on VMS-hosting mafic, felsic volcanic rocks, banded and massive sulfide ores and postmineralization pegmatite vein, we considered that there were two main formation stages for the Qingyuan Cu–Zn deposits; one was exhalative-hydrothermal sedimentation and another was further Cu–Zn enriched by later hydrothermal processes. The timing of the first stage occurred at 2571 ± 6 Ma based on the magmatic zircons in the VMS-hosting mafic volcanic rocks, from which the inherited zircons also indicate the existence of 2.65–3.12 Ga ancient supercrustal rocks in the Qingyuan district. A modern mantle-like δ18Ozircon value of 5.5 ± 0.1‰ (2SD) for this volcanism was well preserved in the inherited core domains of ore samples. It suggests that the mafic volcanics was most likely sourced from partial melting of juvenile crust, e.g., TTG granites. A large-scale metamorphic or hydrothermal event is documented by the recrystallized zircons in sulfide ores. The timing is tightly constrained by the hydrothermal zircon U–Pb ages. They are 2508 ± 4 Ma for the banded ore, 2507 ± 4 Ma for the massive ore and 2508 ± 2 Ma for the postmineralization pegmatite vein. These indistinguishable ages indicate that the 2507 Ma hydrothermal systems played a significant role in the upgrading of the VMS Cu–Zn orebodies. The weighted δ18O values of hydrothermal zircons show a successively increasing trend from 6.0 ± 0.1‰ (2σ) for the banded ore, 6.6 ± 0.2‰ (2σ) for the massive ore to 7.3 ± 0.2‰ (2σ) for the later pegmatite vein. This variation might be induced by gradual inputting of the δ18O-rich oceanic crust and/or oceanic sediment during the hydrothermal cycling system. Considering its modern mantle-like oxygen isotope composition of 2571 Ma volcanism, a submarine volcanic hydrothermal system involving mantle plumes is a preferred setting for the Neoarchean VMS Cu–Zn deposits in the Qingyuan greenstone belt. 相似文献
17.
Economic important minerals and ore deposits are common in hydrothermal altered serpentinized zone. Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) satellite sensor is capable of discrimination of such hydrothermal mineralized zone and detection of hydrothermal altered minerals. In the present study, the hydrothermal altered serpentinized harzburgites of Wadi Hibi area of Northern Oman Mountains have been discriminated by using ASTER VNIR–SWIR spectral bands by image processing methods and the occurrences of Ni-magnesioferrite–magnetite–awaruite in the rocks are studied. The color composite RGB image developed using ASTER spectral bands 8, 4 and 1, mapped well the occurrence of weathered peridotites by pale green to dark blue in colors and discriminated the hydrothermally altered serpentinized rocks by pale brown to dark blue colors due to the strong absorption of OH and Mg–OH molecules that occurred in the serpentine minerals of the rocks in the study area. The ASTER band ratios 4/7, 4/1, and 2/3 × 4/3 RGB images studied are capable of discrimination of hydrothermal mineralized areas more clear by pale blue to purple colors due to the strong absorption of such hydroxyl bearing serpentine minerals. The studied image processing methods are evaluated by applying to the region of Wadi Sarami situated in the Semail ophiolite (Oman). In addition to that, the occurrence of serpentine minerals namely, lizardite and antigorite in the hydrothermally altered serpentinized region are detected qualitatively and quantitatively using Spectral Angle Mapper (SAM) supervised classification image processing method and studied.The interpreted images are verified in the field and checked for the occurrences of minerals including Ni-magnesioferrite, magnetite, pentlandite and awaruite and are confirmed through laboratory studies. Petrographic study of serpentinized harzburgites shows that the rocks consist predominantly of antigorite and lizardite serpentines, olivine and have the opaque minerals assemblage of Ni-magnesioferrite + magnetite + awaruite + pentlandite developed during serpentinization of the rock. The occurrences of such minerals are confirmed by XRD, electron microprobe analyses and spectral measurements in the laboratory.ASTER sensor proved its capability in discriminating the hydrothermal altered serpentinized zone and detecting the mineral occurrences and thus the study recommends the technique to the exploration geologists, scientists and mining geologists for mapping of such rocks and minerals in the similar arid region. 相似文献
18.
Hydrothermal petroleums and heavy tars have been analyzed for polycyclic aromatic hydrocarbons (PAH) with molecular weights greater than that of coronene (300 da). Samples from the hydrothermal systems in the Guaymas Basin (Gulf of California) and in the Escanaba Trough and Middle Valley (Northeastern Pacific) were analyzed by gas chromatography-mass spectrometry and high pressure liquid chromatography with diode-array absorbance detection. Mass spectra and fluorescence spectra were used to characterize the compounds. Several large PAHs with six and more rings were identified among the heavy PAH. Production routes via one-ring build-up and Scholl-condensation are proposed to explain the observed structures. The variations in PAH concentrations and distributions between samples from different locales are a consequence of the hydrothermal conditions of generation, migration, and post-depositional alteration. 相似文献
19.
The recently discovered Zhuxi W–Cu ore deposit is located within the Taqian–Fuchun Ore Belt in the southeastern edge of the Yangtze Block, South China. Its inferred tungsten resources, based on new exploration data, are more than 280 Mt by 2016. At least three paragenetic stages of skarn formation and ore deposition have been recognized: prograde skarn stage; retrograde stage; and hydrothermal sulfide stage. Secondly, greisenization, marmorization and hornfels formation are also observed. Scheelite and chalcopyrite are the dominant metal minerals in the Zhuxi deposit and their formation was associated with the emplacement of granite stocks and porphyry dykes intruded into the surrounding Carboniferous carbonate sediments (Huanglong and Chuanshan formations) and the Neoproterozoic slate and phyllites. The scheelite was mostly precipitated during the retrograde stage, whereas the chalcopyrite was widely precipitated during the hydrothermal sulfide stage. A muscovite 40Ar/39Ar plateau age of about 150 Ma is interpreted as the time of tungsten mineralization and molybdenite Re–Os model ages ranging from 145.9 ± 2.0 Ma to 148.7 ± 2.2 Ma (for the subsequent hydrothermal sulfide stage of activity) as the time of the copper mineralization. Our new molybdenite Re–Os and muscovite 40Ar/39Ar dating results, along with previous zircon U–Pb age data, indicate that the hydrothermal activity from the retrograde stage to the last hydrothermal sulfide stage lasted up to 5 Myr, from 150.6 ± 1.5 to 145.9 ± 1 Ma, and is approximately coeval or slightly later than the emplacement of the associated granite porphyry and biotite granite. The new ages reported here confirm that the Zhuxi tungsten deposit represents one of the Mesozoic magmatic–hydrothermal mineralization events that took place in South China in a setting of lithospheric extension during the Late Jurassic (160–150 Ma). It is suggested that mantle material played a role in producing the Zhuxi W–Cu mineralization and associated magmatism. 相似文献
20.
Uranium deposits form in a variety of settings. They are partially controlled by the secular evolution of Earth processes, including deposits in extension-related settings such as the intra-cratonic Rio Grande rift. Plio-Quaternary volcanism, mineral deposits, and hydrothermal spots occur along the Chihuahua Central Graben. The age of the Sierra de Gomez U-deposit is 1.8 Ma (based on LA-MC-ICP-MS dating on a uranophane monocrystal), which is contemporaneous with the late mineralization event of the Peña Blanca U-deposit, as well as Rio Grande Rift (RGR)-type deposits in Chihuahua and intraplate volcanism. Studies of fluid inclusions in fluorite and late calcite indicate the presence of hydrocarbons and CH4-rich brine. Homogenization temperatures range from 87 to 112 °C, and the mean composition (2.0 mol NaCl and 0.3 mol CaCl with CH4) is comparable to mineralizing brines in MVT deposits and carbonated hydrocarbon reservoirs. Evolution of C and O stable isotopic values for the calcite cement in the Sierra de Gomez Limestone-hosted U deposit illustrates that two separate calcite precipitation events occurred: (1) travertine filling karst structures in the presence of meteoric water and (2) U mineralization during deep hydrothermal fluid circulation that included interactions with a heat source and basement leaching. In a regional context, a metallogenic model suggests that the Chihuahua Trough area is deep enough to generate fluid migration by hydrothermal and/or compaction processes through RGR extensional faults until a favorable trapping horizon is reached. This causes uranium precipitation because water/rock interaction processes generate a local redox barrier. 相似文献