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1.
Major minerals (sulfates, sulfides, quartz) are distributed in different parts of submarine hydrothermal ore deposits. For instance, the abundance of barite increases stratigraphically upwards in the massive orebodies of the Kuroko deposits (black and yellow ores), while quartz is abundant in the lower parts (siliceous ore). The different distribution of barite and quartz in the Kuroko deposits can not be accounted for by thermochemical equilibrium calculations based on the precipitation due to mixing of ascending hydrothermal solutions with ambient cold seawater. In the present study, a coupled fluid flow‐precipitation kinetics model was used to calculate the amounts of quartz, barite, and anhydrite precipitated from a hydrothermal solution mixed with seawater, assuming reasonable values for temperature, precipitation rate, fluid flow velocity, mineral surface area/fluid mass ratio (A/M), and initial concentrations of hydrothermal solution and seawater before mixing occurred. The results indicate that barite precipitates more efficiently than quartz from discharging fluids with relatively higher flow velocity, lower temperatures and under the condition of lower A/M ratios on the seafloor (black ore), whereas quartz precipitates more effectively from solutions with lower flow velocity, higher temperatures and higher A/M ratios beneath the seafloor (siliceous ore) and in the orebody (barite ore, ferruginous chert ore). Anhydrite precipitates in shallow sub‐seafloor environments with lower precipitation rates and higher A/M ratios than barite and higher precipitation rates and lower A/M ratios than quartz. These results explain the observed occurrences of barite, anhydrite, and quartz in the Kuroko deposits. Namely, barite is abundant in black ore and barite ore which formed above the seafloor, anhydrite formed in high‐permeability tuff breccias, and quartz formed in low permeability dacite intrusive bodies in the sub‐seafloor environment. 相似文献
2.
为了探索高渗透性洋壳中高温热液循环系统的形成机制,以数值模拟为手段研究热液循环中的矿物沉淀过程及其对洋壳渗透率的反馈.在热液对流-矿物反应模型中考虑了硬石膏、黄铁矿和黄铜矿的沉淀和溶解反应,基于矿物的溶度积计算矿物的沉淀/溶解量,并将其转换为渗透率的变化.结果显示,黄铁矿和黄铜矿分布于350~380℃等温线范围内,并随着热液温度升高而逐渐向海底推移.海水被加热及与热液混合过程中沉淀出硬石膏,在热液上升通道两侧形成低渗透性的烟囱状结构,降低了海水-热液混合程度从而使热液温度升高.高温热液通道建立后,便会有更多的金属物质随着高温热液被运输至浅层洋壳或海底.模拟结果为理解海底高温热液喷口的形成机制提供了借鉴. 相似文献
3.
原始的海水成分、基岩的组分及结构、热源性质等因素决定着现代海底热液喷口系统的流体成分, 同时, 各种地质构造背景下的岩浆脱气作用也在不同程度上影响热液流体的组成.热液流体一旦喷出海底, 就能形成不同类型的热液沉积体, 包括高温流体形成的金属硫化物或硫酸盐烟囱体、热液丘以及由低温弥散流及非浮力羽流形成的含金属沉积物堆积体.高温烟囱体的形成受控于海水和热液的混合比例, 常常表现为典型的两阶段模式, 即先形成环状硬石膏表层, 然后在其内部发生富Cu硫化物的沉淀.这一模式在更大尺度上也可以观察到, 如TAG热液丘.含金属沉积物遍布海底, 除热液羽流外, 金属硫化物烟囱体在氧化环境中氧化蚀变的产物也是其重要来源.生物的活动贯穿于现代热液过程的始终, 并在烟囱体的形成、分解以及羽流的扩散沉淀过程中起到了重要作用.当前, 热液生物矿化机理、Lost City型热液场以及超慢速扩张洋脊的有关研究是海底这一系统研究的热点, 前两者研究能使人们更好地理解地球早期的演化和生命的起源, 而后者的考察和研究能进一步丰富海底热液成矿理论, 并有助于寻找更大规模的热液矿体. 相似文献
4.
Black smoker chimneys and biological vent communities have been identified at many sites on the deep seafloor, particularly along oceanic spreading centers. We report the largest and oldest known, microbe-rich sub-meter-sized black smoker chimneys and mounds from a 1.43 billion-year old sulfide deposit in a continental graben in northern China. These chimneys are especially well preserved, with characteristic morphology, internal textures and internal cylindrical mineralogical zonation. Four main types of chimneys are distinguished on textural and mineralogical criteria, exhibiting either Zn–Fe-sulfide or Pb–Zn–Fe-sulfide internal cylindrical mineralogical zones. The chimneys mark vent sites in submarine grabens indicating focused flow-venting processes. The fossil chimneys have mineralogical and geological evolutionary features similar to their counterparts on the modern seafloor and other submarine hydrothermal vents. Black smoker vent fluids and seafloor tectonism played important roles for formation of the massive sulfide deposits in the Mesoproterozoic.We also report the first known, remarkably diverse assemblage of fossil microbialites from around and inside Precambrian vent chimneys, demonstrating that Proterozoic life flourished around submarine hot vents and deep within the chimney vent passages. Filamentous, spherical, rod, and coccus-shaped fossil microbes are preserved preferentially on sulfide precipitates. Based on the depth and setting of the fossil biota, the organisms that produced the microbialites were likely sulfate-reducing chemosynthetic and thermophyllic microbes. Textural and mineralogical evidence shows that biomineralization processes enhanced chimney growth and sulfide precipitation.Close association of microorganisms with sulfide chimneys in modern deep-sea hydrothermal vents and younger ophiolites has sparked speculation about whether life may have originated at similar vents. However, little is known about fossil equivalents of vent microfossils and black smoker chimneys from Earth's early evolution. The fossilized microorganisms from the Gaobanhe black smoker chimney sulfide deposits include thread-like filaments with branching and twisted forms and preserved organic carbon, representing fossilized remnants of microbial mats metabolized at high temperatures characteristic of venting fluids. The preservation of fossil microorganisms provides evidence that microbial populations were closely associated with black smoker chimneys in Earth's early history. The microbial population clearly constitutes the site for mediating mineral formation. These ancient microbial fossils lead to a much better understanding of early life on the deep seafloor. The discovery of the Mesoproterozoic microfossils within black-smoker hydrothermal chimneys indicates that hydrothermal activity around sea-floor vents supported dense microbial communities, and supports speculation that vent sites may have hosted the origin of life. 相似文献
5.
Microchemical analyses of rare earth element (REE) concentrations and Sr and S isotope ratios of anhydrite are used to identify sub-seafloor processes governing the formation of hydrothermal fluids in the convergent margin Manus Basin, Papua New Guinea. Samples comprise drill-core vein anhydrite and seafloor massive anhydrite from the PACMANUS (Roman Ruins, Snowcap and Fenway) and SuSu Knolls (North Su) active hydrothermal fields. Chondrite-normalized REE patterns in anhydrite show remarkable heterogeneity on the scale of individual grains, different from the near uniform REEN patterns measured in anhydrite from mid-ocean ridge deposits. The REEN patterns in anhydrite are correlated with REE distributions measured in hydrothermal fluids venting at the seafloor at these vent fields and are interpreted to record episodes of hydrothermal fluid formation affected by magmatic volatile degassing. 87Sr/86Sr ratios vary dramatically within individual grains between that of contemporary seawater and that of endmember hydrothermal fluid. Anhydrite was precipitated from a highly variable mixture of the two. The intra-grain heterogeneity implies that anhydrite preserves periods of contrasting hydrothermal versus seawater dominant near-seafloor fluid circulation. Most sulfate δ34S values of anhydrite cluster around that of contemporary seawater, consistent with anhydrite precipitating from hydrothermal fluid mixed with locally entrained seawater. Sulfate δ34S isotope ratios in some anhydrites are, however, lighter than that of seawater, which are interpreted as recording a source of sulfate derived from magmatic SO2 degassed from underlying felsic magmas in the Manus Basin. The range of elemental and isotopic signatures observed in anhydrite records a range of sub-seafloor processes including high-temperature hydrothermal fluid circulation, varying extents of magmatic volatile degassing, seawater entrainment and fluid mixing. The chemical and isotopic heterogeneity recorded in anhydrite at the inter- and intra-grain scale captures the dynamics of hydrothermal fluid formation and sub-seafloor circulation that is highly variable both spatially and temporally on timescales over which hydrothermal deposits are formed. Microchemical analysis of hydrothermal minerals can provide information about the temporal history of submarine hydrothermal systems that are variable over time and cannot necessarily be inferred only from the study of vent fluids. 相似文献
6.
Ryohei Suzuki Jun-Ichiro Ishibashi Miwako Nakaseama Uta Konno Urumu Tsunogai Kaul Gena Hitoshi Chiba 《Resource Geology》2008,58(3):267-288
The Yonaguni Knoll IV hydrothermal vent field (24°51′N, 122°42′E) is located at water depths of 1370–1385 m near the western edge of the southern Okinawa Trough. During the YK03–05 and YK04–05 expeditions using the submersible Shinkai 6500, both hydrothermal precipitates (sulfide/sulfate/carbonate) and high temperature fluids (Tmax = 328°C) presently venting from chimney‐mound structures were extensively sampled. The collected venting fluids had a wide range of chemistry (Cl concentration 376–635 mmol kg?1), which is considered as evidence for sub‐seafloor phase separation. While the Cl‐enriched smoky black fluids were venting from two adjacent chimney‐mound structures in the hydrothermal center, the clear transparent fluids sometimes containing CO2 droplet were found in the peripheral area of the field. This distribution pattern could be explained by migration of the vapor‐rich hydrothermal fluid within a porous sediment layer after the sub‐seafloor phase separation. The collected hydrothermal precipitates demonstrated a diverse range of mineralization, which can be classified into five groups: (i) anhydrite‐rich chimneys, immature precipitates including sulfide disseminations in anhydrite; (ii) massive Zn‐Pb‐Cu sulfides, consisting of sphalerite, wurtzite, galena, chalcopyrite, pyrite, and marcasite; (iii) Ba‐As chimneys, composed of barite with sulfide disseminations, sometimes associated with realgar and orpiment overgrowth; (iv) Mn‐rich chimneys, consisting of carbonates (calcite and magnesite) and sulfides (sphalerite, galena, chalcopyrite, alabandite, and minor amount of tennantite and enargite); and (v) pavement, silicified sediment including abundant native sulfur or barite. Sulfide/sulfate mineralization (groups i–iii) was found in the chimney–mound structure associated with vapor‐loss (Cl‐enriched) fluid venting. In contrast, the sulfide/carbonate mineralization (group iv) was specifically found in the chimneys where vapor‐rich (Cl‐depleted) fluid venting is expected, and the pavement (group v) was associated with diffusive venting from the seafloor sediment. This correspondence strongly suggests that the subseafloor phase separation plays an important role in the diverse range of mineralization in the Yonaguni IV field. The observed sulfide mineral assemblage was consistent with the sulfur fugacity calculated from the FeS content in sphalerite/wurtzite and the fluid temperature for each site, which suggests that the shift of the sulfur fugacity due to participation of volatile species during phase separation is an important factor to induce diverse mineralization. In contrast, carbonate mineralization is attributed to the significant mixing of vapor‐rich hydrothermal fluid and seawater. A submarine hydrothermal system within a back‐arc basin in the continental margin may be considered as developed in a geologic setting favorable to a diverse range of mineralization, where relatively shallow water depth induces sub‐seafloor phase separation of hydrothermal fluid, and sediment accumulation could enhance migration of the vapor‐rich hydrothermal fluid. 相似文献
7.
Sulfide sulfur in mid-oceanic ridge hydrothermal vents is derived from leaching of basaltic-sulfide and seawater-derived sulfate that is reduced during high temperature water rock interaction. Conventional sulfur isotope studies, however, are inconclusive about the mass-balance between the two sources because 34S/32S ratios of vent fluid H2S and chimney sulfide minerals may reflect not only the mixing ratio but also isotope exchange between sulfate and sulfide. Here, we show that high-precision analysis of S-33 can provide a unique constraint because isotope mixing and isotope exchange result in different Δ33S (≡δ33S-0.515 δ34S) values of up to 0.04‰ even if δ34S values are identical. Detection of such small Δ33S differences is technically feasible by using the SF6 dual-inlet mass-spectrometry protocol that has been improved to achieve a precision as good as 0.006‰ (2σ).Sulfide minerals (marcasite, pyrite, chalcopyrite, and sphalerite) and vent H2S collected from four active seafloor hydrothermal vent sites, East Pacific Rise (EPR) 9-10°N, 13°N, and 21°S and Mid-Atlantic Ridge (MAR) 37°N yield Δ33S values ranging from −0.002 to 0.033 and δ34S from −0.5‰ to 5.3‰. The combined δ34S and Δ33S systematics reveal that 73 to 89% of vent sulfides are derived from leaching from basaltic sulfide and only 11 to 27% from seawater-derived sulfate. Pyrite from EPR 13°N and marcasite from MAR 37°N are in isotope disequilibrium not only in δ34S but also in Δ33S with respect to associated sphalerite and chalcopyrite, suggesting non-equilibrium sulfur isotope exchange between seawater sulfate and sulfide during pyrite precipitation. Seafloor hydrothermal vent sulfides are characterized by low Δ33S values compared with biogenic sulfides, suggesting little or no contribution of sulfide from microbial sulfate reduction into hydrothermal sulfides at sediment-free mid-oceanic ridge systems. We conclude that 33S is an effective new tracer for interplay among seawater, oceanic crust and microbes in subseafloor hydrothermal sulfur cycles. 相似文献
8.
Teresa Suter Bowers Karen L. Von Damm John M. Edmond 《Geochimica et cosmochimica acta》1985,49(11):2239-2252
Chemical analyses yielding elemental concentrations of major and minor elements of four hot springs on the East Pacific Rise at 21°N and 10 hot springs from the southern trough of the Guaymas Basin, Gulf of California provide a basis for thermodynamic modeling of conductive cooling of the hydrothermal endmembers, mixing of the hydrothermal endmember with seawater, and reaction of an EPR-type fluid with sediment of bulk chemical composition corresponding to unaltered sediment from DSDP hole 477 in the Guaymas Basin. Results of the calculations indicate that conductive cooling of endmember fluids within closed chimneys and conduits accounts for the solution composition of one vent on the East Pacific Rise and several vents in Guaymas Basin. Mixing of the hydrothermal fluids with seawater yields a prediction of mineral assemblages closely approximating those observed in samples of chimneys from the East Pacific Rise and drill cores in Guaymas Basin. The hypothesis that Guaymas Basin hydrothermal fluids result from interaction of an EPR-type fluid with sediment cover in Guaymas Basin is supported by calculations which predict an increase in pH to a value similar to Guaymas Basin fluids, an order-of-magnitude decrease in metal concentrations, and an excellent agreement between predicted mineral assemblages as a function of extent of interaction with sediment, and observed mineral assemblage distribution with depth. 相似文献
9.
Geochemical constraints on chemolithoautotrophic metabolism by microorganisms in seafloor hydrothermal systems 总被引：10，自引：0，他引：10
Mixing of hydrothermal fluids and seawater at the ocean floor, combined with slow reaction kinetics for oxidation/reduction reactions, provides a source of metabolic energy for chemolithotrophic microorganisms which are the primary biomass producers for an extensive submarine ecosystem that is essentially independent of photosynthesis. Thermodynamic models are used to explore geochemical constraints on the amount of metabolic energy potentially available from chemosynthetic reactions involving S, C, Fe, and Mn compounds during mixing of hydrothermal fluids with seawater. For the vent fluid used in the calculations (EPR 21 degrees N OBS), the model indicates that mixing environments are favorable for oxidation of H2S, CH4, Fe2+ and Mn2+ only below approximately 38 degrees C, with methanogenesis and reduction of sulfate or S degrees favored at higher temperatures, suggesting that environments dominated by mixing provide habitats for mesophilic (but not thermophilic) aerobes and thermophilic (but not mesophilic) anaerobes. A maximum of approximately 760 cal per kilogram vent fluid is available from sulfide oxidation while between 8 and 35 cal/kg vent fluid is available from methanotrophy, methanogenesis, oxidation of Fe or Mn, or sulfate reduction. The total potential for chemosynthetic primary production at deep-sea hydrothermal vents globally is estimated to be about 10(13) g biomass per year, which represents approximately 0.02% of the global primary production by photosynthesis in the oceans. Thermophilic methanogens and sulfate- and S degree-reducers are likely to be the predominant organisms in the walls of vent chimneys and in the diffuse mixing zones beneath warm vents, where biological processes may contribute to the high methane concentrations of vent fluids and heavy 34S/32S ratios of vent sulfide minerals. The metabolic processes taking place in these systems may be analogs of the first living systems to evolve on the Earth. 相似文献
10.
Katrina J. Edwards Thomas M. McCollom Peter R. Buseck 《Geochimica et cosmochimica acta》2003,67(15):2843-2856
We present results of incubation studies conducted at low temperatures (∼4°C) in the vicinity of a seafloor hydrothermal vent system. We reacted Fe-, S-, Cu-, and Zn-bearing minerals including pyrite, marcasite, chalcopyrite, sphalerite, elemental sulfur, and a portion of a natural chimney sulfide structure for 2 months at the Main Endeavour Segment of the Juan de Fuca Ridge in the Pacific Ocean. Our study utilizes Fluorescent In Situ Hybridizations (FISH), Scanning and Transmission Electron Microscopy (SEM, TEM), and light microscopic analysis. The surfaces of these minerals are solely colonized by Bacteria and not by Archaea. Colonization densities vary over an order of magnitude with the following sequence: elemental sulfur > chimney sulfide > marcasite > pyrite > sphalerite > chalcopyrite, and correspond well with the abiotic oxidation kinetics of these materials, excepting elemental sulfur, which is both the least reactive to oxidizing species and the most heavily colonized. Colonization densities also correspond with apparent degree of reaction (dissolution pitting + accumulation of secondary alteration products). Heavy accumulations of secondary Fe oxides on Fe-bearing minerals, most notably on the chimney sulfide, form in situ as the result of mineral dissolution and the activity of neutrophilic Fe-oxidizing bacteria. Results suggest that mineral-oxidizing bacteria play a prominent role in weathering of seafloor sulfide deposits, and that microbial utilization of mineral substrates contributes to biomass production in seafloor hydrothermal environments. 相似文献
11.
To characterize the hydrothermal processes of East Pacific rise at 9o-10oN, sulfide mineral compositions, textural, and geochemical features of chimney ores were studied using ore microscope, scanning electron microscope, X-ray diffraction analysis, and electron microprobe techniques. Results show that there are three mineral assemblages for the hydrothermal chimney ores, namely: (i) anhydrite marcasite pyrite, (ii) pyrite sphalerite chalcopyrite, and (iii) chalcopyrite bornite digenite covellite. Mineral assemblages, zonational features, and geochemical characteristics of the ore minerals indicate that ore fluid temperature changed from low to high then to low with a maximum temperature up to 400 ℃. The chimney is a typical black smoker. The initial structure of the chimney was formed by the precipitation of anhydrites, and later the sulfides began to precipitate in the inner wall. 相似文献
12.
K.L. Von Damm C.M. Parker M.D. Lilley D.A. Clague 《Geochimica et cosmochimica acta》2005,69(21):4971-4984
The composition and temperature of vent fluids sampled from the active hydrothermal system in Escanaba Trough, Gorda Ridge in 2000 and 2002 remain unchanged from the only time this field was previously sampled, in 1988. ODP Leg 169 drilled nine bore holes at this site in 1996, some within meters of the vents, yet this disturbance has not impacted the measured compositions or temperatures of the fluids exiting at the seafloor. The fluids have maximum measured temperatures of 218°C and contain ∼20% more chloride than local ambient seawater. Our interpretation is that the fluid compositions are generated by supercritical phase separation of seawater, with much of the water-rock reaction occurring within the ∼400m thick sedimentary section that overlies the basalt at this site. The ODP drilling results provide information on the mineralogy and composition of materials below the seafloor, as well as direct constraints not typically available on the physical conditions occurring below the seafloor hydrothermal system. Calculations utilizing geochemical modeling software suggest the fluids are close to saturation with a suite of minerals found subsurface, suggesting equilibrium between the fluids and substrate. These results provide an explanation for why the fluids have remained chemically stable for 14 yrs. The pore water data from drilling suggest that the hydrology and chemistry of the hydrothermal system are much more complex within the sediment cover than would be expected from the surface manifestations of the hydrothermal system. While the pore waters have chloride contents both greater and less than the local seawater, only fluids with higher chloride contents vent at the seafloor. Our calculations suggest that at the current conditions the “brines” (fluids with chlorinity greater than seawater) are actually less dense than the “vapors” (fluids with chlorinity less than seawater). These density relationships may provide an explanation for why the “brines” are now venting preferentially to the “vapors,” a situation opposite to what is usually observed or inferred. 相似文献
13.
Here, we report the first documented occurrences of “invisible” gold and silver in seafloor sulfide deposits from an active hydrothermal system on the Central Indian Ridge. A detailed mineralogical and geochemical study of polymetallic sulfides from the Edmond vent field was conducted in order to identify controls on the distribution of precious metals. Bulk samples (N = 18) contain up to 18.7 ppm Au and 1450 ppm Ag, with average concentrations of 2.3 ppm Au and 218.9 ppm Ag. Among them, several Zn-rich chimney fragments and anhydrite-dominated ore samples have higher contents of precious metals than Fe-Cu-rich massive sulfides and silica-rich hydrothermal precipitates. Native gold grains are mainly associated with sphalerite, anhydrite, barite and Fe-oxyhydroxides. Abundant submicroscopic Au-Ag alloys tend to occur along grain boundaries between Cu-Fe sulfides and tennantite, or close to the rims of Fe-poor sphalerite. In contrast to primary electrum with high Ag/Au ratios, the absence of detectable silver in high-purity gold indicates that secondary Au enrichment has probably occurred after a direct co-precipitation with Zn-rich mineral assemblages upon cooling and mixing of vent fluids with cold seawater. A suite of late-stage Ag-rich phases, including argentotennantite, pearceite and acanthite, occur as crack-filling veinlets and patches in low-temperature fahlores, or as tiny inclusions enclosed by pyrite, chalcopyrite and colloform sphalerite. By using HRTEM combined with HAADF-STEM imaging, we have found out that silver is also present in significant quantities as discrete colloidal nanoparticles in tennantite. Minor native copper is closely associated with altered chalcopyrite, sphalerite and covellite, exhibiting signs of dissolution, recrystallization and reprecipitation. Extensive hydrothermal reworking resulted from a long history of high-temperature venting in this field, together with post-depositional supergene replacement processes (involving oxidation, leaching or coupled dissolution-reprecipitation mechanisms facilitated by a permeable porosity generated in primary Cu-Fe sulfides) are considered to be important for the remobilization and local reconcentration of early-formed precious metals, and may have been responsible for the formation of relatively coarse-grained native gold or silver within recrystallized massive sulfides and chimney debris. 相似文献
14.
Durbar RAY Dalayya KOTA Pranab DAS L. Surya PRAKASH V.D. KHEDEKAR Anil L. PAROPKARI Abhay V. MUDHOLKAR 《《地质学报》英文版》2014,88(1):213-225
An extinct hydrothermal barite-silica chimney from the Franklin Seamount of the Woodlark Basin, in the southwestern Pacific Ocean, was investigated for mineral distribution and geochemical composition. Six layers on either side of the orifice of a chimney show significant disparity in color, mineral assemblage and major element composition. Electron microscope(SEM) images reveal that the peripheral wall of the chimney is composed of colloform silica, suggesting that incipient precipitation of silica-saturated hydrothermal fluid initiated the development of the chimney wall. Intermediate layers, between the exterior wall and the inner fluid-orifice, dominate with barite and sulfides. Low Sr-to-Ba ratios(SrO/BaO = 0.015–0.017) indicate restricted fluid-seawater mixing, which causes relatively high-temperature formation of the intermediate layers. Whereas the innermost layer bordering the chimney orifice is characterized by more silica and a higher Sr-to-Ba ratio(SrO/BaO = 0.023), could have formed due to a paragenetic shift from a high-temperature active phase to a cooler waning stage of formation. A paragenetic shift is also probably responsible for the change in mineral formation mechanism that resulted in the textural variation of barite and colloform silica developed during different growth phases of this barite-silica chimney. 相似文献
15.
Zahra Badrzadeh Timothy J. Barrett Jan M. Peter Domingo Gimeno Mossaieb Sabzehei Mehraj Aghazadeh 《Mineralium Deposita》2011,46(8):905-923
The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ34S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ34S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones. 相似文献
16.
Andrea Koschinsky Richard SeifertPeter Halbach Michael BauSabine Brasse Leandro M de CarvalhoNuno M Fonseca 《Geochimica et cosmochimica acta》2002,66(8):1409-1427
Low-temperature (<13°C) diffuse hydrothermal fluids were sampled directly at the seafloor with a specially designed Hydro Bottom Station in the North Fiji Basin and analyzed for gases, major and minor elements, and a large number of trace metals. The fluids were significantly enriched in CO2, Si, Li, Rb, Cs, Ba, Mn, and several trace metals compared to ambient seawater, had high CH4 and H2S concentrations, and had a slightly decreased salinity. Calculated end-member concentrations of the low-temperature fluids show a strong similarity to the neighboring hot vents, implying that the diffuse fluids are hot vent waters diluted by seawater. According to the chemical composition, the sampled fluids derive from vapor-phase fluids produced by subseafloor boiling and phase separation. Compared to hot vents from other regions, Mn, Fe, and other trace metal concentrations are low. Subsurface metal sulfide precipitation during cooling and dilution with seawater has further decreased the dissolved metal contents of the diffuse fluids, thus creating a very favorable environment for the hydrothermal fauna, as indicated by a very low Fe/H2S ratio. Therefore, the fluids support high bioproductivity but no hydrothermal mineral precipitation. The emanation of the condensed vapor phase appears to have been stable during the past 10 years; however, the occurrence of metal sulfide particles in some fluid and sediment samples and small areas of dead fauna indicate that the hydrothermal system may be evolving toward the emanation of the stored brine phase. 相似文献
17.
The discovery of ultramafic hosted hydrothermal systems at Rainbow (36°N MAR) and Lost City, a vent site approximately 15 km west of the MAR at 30°N, provides unique perspectives on chemical and heat-generating processes associated with serpentinization at a range of chemical and physical conditions. Heat balance calculations together with constraints imposed by geochemical modeling indicate that significant changes in temperature are not likely to occur at either vent system as a result of the exothermic nature of olivine hydrolysis. At Rainbow, the relatively high temperatures in subseafloor reaction zones (in excess of 400°C), which must be linked to magmatic processes, inhibit olivine hydrolysis, effectively precluding mineralization-induced heating effects. Geochemical modeling of the Lost City vent fluids indicates temperatures in excess of those measured (40-75°C). The relatively high subseafloor temperatures (∼ 200 ± 50°C) requires conductive cooling of the fluids on ascent to the seafloor—a scenario in keeping with the mineralization of chimney structures actually observed. Although the intermediate temperatures predicted for subseafloor reaction zones at Lost City could be expected to enhance olivine to serpentine conversion, dissolved Cl, K/Cl and Na/Cl ratios of the Lost City vent fluids are virtually unchanged from seawater values and indicate little hydration of olivine, which is a necessary condition for exothermic heat generation by serpentinization. Apparently the fluid/rock mass ratio is too high or fluid residence times too low for this to occur to any significant extent. Thus, in spite of the off-axis location of the Lost City vents and apparent lack of a localized heat source, mineralization reactions likely play an insignificant role in accounting for hydrothermal circulation. It is more likely that tectonic processes associated with the slow spreading MAR, permit access of seawater to relatively deep and still hot lithospheric units and/or near axis magmatic heat sources, before venting. Additional chemical and physical (temperature, flow rate) data for Lost City and similar hydrothermal systems are needed to test key elements of the proposed model. 相似文献
18.
The coexistence of magmatic anhydrite and sulfide minerals in non-arc-related mafic magmas has only rarely been documented. Likewise the S isotope fractionation between sulfate and sulfide in mafic rocks has infrequently been measured. In the Kharaelakh intrusion associated with the world-famous Noril’sk ore district in Siberia coexisting magmatic anhydrite and sulfide minerals have been identified. Sulfur isotope compositions of the anhydrite-sulfide assemblages have been measured via both ion microprobe and conventional analyses to help elucidate the origin of the anhydrite-sulfide pairs. Magmatic anhydrite and chalcopyrite are characterized by δ34S values between 18.8‰ and 22.8‰, and 9.3‰ and 13.2‰, respectfully. Coexisting anhydrite and chalcopyrite show Δ values that fall between 8.5‰ and 11.9‰. Anhydrite in the Kharaelakh intrusion is most readily explained by the assimilation of sulfate from country rocks; partial reduction to sulfide led to mixing between sulfate-derived sulfide and sulfide of mantle origin. The variable anhydrite and sulfide δ34S values are a function of differing degrees of sulfate reduction, variable mixing of sulfate-derived and mantle sulfide, incomplete isotopic homogenization of the magma, and a lack of uniform attainment of isotopic equilibrium during subsolidus cooling. The δ34S values of sulfide minerals have changed much less with cooling than have anhydrite values due in large part to the high sulfide/sulfate ratio. Variations in both sulfide and anhydrite δ34S values indicate that isotopically distinct domains existed on a centimeter scale. Late stage hydrothermal anhydrite and pyrite also occur associated with Ca-rich hydrous alteration assemblages (e.g., thomsonite, prehnite, pectolite, epidote, xonotlite). δ34S values of secondary hydrothermal anhydrite and pyrite determined by conventional analyses are in the same range as those of the magmatic minerals. Anhydrite-pyrite Δ values are in the 9.1-10.1‰ range, and are smaller than anticipated for the low temperatures indicated by the silicate alteration assemblages. The small Δ values are suggestive of either sulfate-sulfide isotopic disequilibrium or closure of the system to further exchange between ∼550 and 600 °C. Our results confirm the importance of the assimilation of externally derived sulfur in the generation of the elevated δ34S values in the Kharaelakh intrusion, but highlight the sulfur isotopic variability that may occur in magmatic systems. In addition, our results confirm the need for more precise experimental determination of sulfate-sulfide sulfur isotope fractionation factors in high-T systems. 相似文献
19.
庐枞盆地中发育一些大中型硫铁矿床,曾长期被认为是与次火山岩有关的中低温热液成因。本文从矿床层控特点、矿体形态产状、矿石沉积组构、矿物组合及其生成顺序、矿化分带、包裹体及同位素地球化学等诸方面,证明它们具显著的火山喷气沉积成因特征,并受到后期热液叠加改造。提出了大鲍庄式陆相火山喷气沉积-热液叠加改造型硫铁矿的成矿模式。 相似文献
20.
The ultramafic-hosted Logatchev Hydrothermal Field (LHF) at 15°N on the Mid-Atlantic Ridge and the Arctic Gakkel Ridge (GR) feature carbonate precipitates (aragonite, calcite, and dolomite) in voids and fractures within different types of host rocks. We present chemical and Sr isotopic compositions of these different carbonates to examine the conditions that led to their formation. Our data reveal that different processes have led to the precipitation of carbonates in the various settings. Seawater-like 87Sr/86Sr ratios for aragonite in serpentinites (0.70909 to 0.70917) from the LHF are similar to those of aragonite from the GR (0.70912 to 0.70917) and indicate aragonite precipitation from seawater at ambient conditions at both sites. Aragonite veins in sulfide breccias from LHF also have seawater-like Sr isotope compositions (0.70909 to 0.70915), however, their rare earth element (REE) patterns show a clear positive europium (Eu) anomaly indicative of a small (< 1%) hydrothermal contribution. In contrast to aragonite, dolomite from the LHF has precipitated at much higher temperatures (~ 100 °C), and yet its 87Sr/86Sr ratios (0.70896 to 0.70907) are only slightly lower than those of aragonite. Even higher temperatures are calculated for the precipitation of deformed calcite veins in serpentine–talc fault schists form north of the LHF. These calcites show unradiogenic 87Sr/86Sr ratios (0.70460 to 0.70499) indicative of precipitation from evolved hydrothermal fluids. A simple mixing model based on Sr mass balance and enthalpy conservation indicates strongly variable conditions of fluid mixing and heat transfers involved in carbonate formation. Dolomite precipitated from a mixture of 97% seawater and 3% hydrothermal fluid that should have had a temperature of approximately 14 °C assuming that no heat was transferred. The much higher apparent precipitation temperatures based on oxygen isotopes (~ 100 °C) may be indicative of conductive heating, probably of seawater prior to mixing. The hydrothermal calcite in the fault schist has precipitated from a mixture of 67% hydrothermal fluid and 33% seawater, which should have had an isenthalpic mixing temperature of ~ 250 °C. The significantly lower temperatures calculated from oxygen isotopes are likely due to conductive cooling of hydrothermal fluid discharging along faults. Rare earth element patterns corroborate the results of the mixing model, since the hydrothermal calcite, which formed from waters with the greatest hydrothermal contribution, has REE patterns that closely resemble those of vent fluids from the LHF. Our results demonstrate, for the first time, that (1) precipitation from pure seawater, (2) conductive heating of seawater, and (3) conductive cooling of hydrothermal fluids in the sub-seafloor all can lead to carbonate precipitation within a single ultramafic-hosted hydrothermal system. 相似文献