Zinc stable isotopes in seafloor hydrothermal vent fluids and chimneys

Many of the heaviest and lightest natural zinc (Zn) isotope ratios have been discovered in hydrothermal ore deposits. However, the processes responsible for fractionating Zn isotopes in hydrothermal systems are poorly understood. In order to better assess the total range of Zn isotopes in hydrothermal systems and to understand the factors which are responsible for this isotopic fractionation, we have measured Zn isotopes in seafloor hydrothermal fluids from numerous vents at 9–10°N and 21°N on the East Pacific Rise (EPR), the TAG hydrothermal field on the Mid-Atlantic Ridge, and in the Guaymas Basin. Fluid δ⁶⁶Zn values measured at these sites range from + 0.00‰ to + 1.04‰. Of the many physical and chemical parameters examined, only temperature was found to correlate with fluid δ⁶⁶Zn values. Lower temperature fluids (< 250 °C) had both heavier and more variable δ⁶⁶Zn values compared to higher temperature fluids from the same hydrothermal fields. We suggest that subsurface cooling of hydrothermal fluids leads to precipitation of isotopically light sphalerite (Zn sulfide), and that this process is a primary cause of Zn isotope variation in hydrothermal fluids. Thermodynamic calculations carried out to determine saturation state of sphalerite in the vent fluids support this hypothesis with isotopically heaviest Zn found in fluids that were calculated to be saturated with respect to sphalerite. We have also measured Zn isotopes in chimney sulfides recovered from a high-temperature (383 °C) and a low-temperature (203 °C) vent at 9–10°N on the EPR and, in both cases, found that the δ⁶⁶Zn of chimney minerals was lighter or similar to the fluid δ⁶⁶Zn. The first measurements of Zn isotopes in hydrothermal fluids have revealed large variations in hydrothermal fluid δ⁶⁶Zn, and suggest that subsurface Zn sulfide precipitation is a primary factor in causing variations in fluid δ⁶⁶Zn. By understanding how chemical processes that occur beneath the seafloor affect hydrothermal fluid δ⁶⁶Zn, Zn isotopes may be used as a tracer for studying hydrothermal processes.     

Vent fluid chemistry in Bahía Concepción coastal submarine hydrothermal system, Baja California Sur, Mexico

Shallow submarine hydrothermal activity has been observed in the Bahía Concepción bay, located at the Gulf coast of the Baja California Peninsula, along faults probably related to the extensional tectonics of the Gulf of California region. Diffuse and focused venting of hydrothermal water and gas occurs in the intertidal and shallow subtidal areas down to 15 m along a NW–SE-trending onshore–offshore fault. Temperatures in the fluid discharge area vary from 50 °C at the sea bottom up to 87 °C at a depth of 10 cm in the sediments.Chemical analyses revealed that thermal water is enriched in Ca, As, Hg, Mn, Ba, HCO₃, Li, Sr, B, I, Cs, Fe and Si, and it has lower concentrations of Cl, Na, SO₄ and Br than seawater. The chemical characteristics of the water samples indicate the occurrence of mixing between seawater and a thermal end-member. Stable isotopic oxygen and hydrogen composition of thermal samples plot close to the Local Meteoric Water Line on a mixing trend between a thermal end-member and seawater. The composition of the thermal end-member was calculated from the chemistry of the submarine samples data by assuming a negligible amount of Mg for the thermal end-member. The results of the mixing model based on the chemical and isotopic composition indicate a maximum of 40% of the thermal end-member in the submarine vent fluid.Chemical geothermometers (Na/Li, Na–K–Ca and Si) were applied to the thermal end-member concentration and indicate a reservoir temperature of approximately 200 °C. The application of K–Mg and Na/Li geothermometers for vent fluids points to a shallow equilibrium temperature of about 120 °C.Results were integrated in a hydrogeological conceptual model that describes formation of thermal fluids by infiltration and subsequent heating of meteoric water. Vent fluid is generated by further mixing with seawater.     

He, Ne and Ar isotope compositions of fluid inclusions in hydrothermal sulfides from the TAG hydrothermal field Mid-Atlantic Ridge

Helium, neon and argon isotope compositions of fluid inclusions have been measured in hydrothermal sulfide samples from the TAG hydrothermal field at the Mid-Atlantic Ridge. Fluid-inclusion³He/⁴He ratios are 2.2—13.3 times the air value (Ra), and with a mean of 7.2 Ra. Comparison with the local vent fluids (³He/⁴He=7.5—8.2 Ra) and mid-ocean ridge basalt values (³He/⁴He=6—11 Ra) shows that the variation range of³He/⁴He ratios from sulfide-hosted fluid inclusions is significantly large. Values for²⁰Ne/²²Ne are from 10.2 to 11.4, which are significantly higher than the atmospheric ratio (9.8). And fluid-inclusion⁴⁰Ar/³⁶Ar ratios range from 287 to 359, which are close to the atmospheric values (295.5). These results indicate that the noble gases of fluid inclusions in hydrothermal sulfides are a mixture of mantle- and seawater-derived noble gases; the partial mantle-derived components of trapped hydrothermal fluids may be from the lower mantle; the helium of fluid inclusions is mainly from upper mantle; and the Ne and Ar components are mainly from seawater.     

Nontronite from a low-temperature hydrothermal system on the Juan de Fuca Ridge

A deposit of Fe-rich, Al-poor, hydrothermal nontronite was recovered from the Juan de Fuca Ridge. Analyses show the deposit to be mineralogically and chemically similar to nontronite described at other oceanic localities. The deposit is located near the tip of a propagating segment of the Juan de Fuca Ridge. Rare earth elements and Sr isotopes indicate that the nontronite precipitated from seawater. A formation temperature of 57°C is suggested by oxygen isotopic composition. The low-temperature nontronite deposits apparently form from newly established hydrothermal systems associated with the propagating rift segment. More mature hydrothermal systems that deposit sulfide on the seafloor may develop from these low-temperature systems.     

Growth of large sulfide structures on the endeavour segment of the Juan de Fuca ridge

Mapping and sampling with DSRV “Alvin” has established that sulfide blocks 0.5 m across, dredged from the axial valley of the Endeavour Segment at 47°57′N, are samples of unusually large sulfide structures. The steep-sided structures, up to 30 m in length, 20 m in height, and 10–15 m across, are localized by venting along normal faults at the base of the western axial valley wall, and are distributed for about 200 m along strike paralleling the 020 trend of the ridge crest. High-temperature fluids (350 to more than 400°C) pass through the massive sulfide structures and enter seawater through small, concentric “nozzle-like” features projecting from the top or the sides of the larger vent structures. Diffuse, low-temperature flow is pervasive in the vicinity of the active sulfide structures, exiting from basalt and sulfide surfaces alike. Evidence of recent volcanic activity is sparse.The two largest samples taken with the dredge would not have been recoverable using the submersible. These samples represent massive, complex portions of the sulfide structures which were not closely associated with rapid high-temperature fluid flow at the time of sampling; they contain textural evidence of sealed hydrothermal fluid exit channels. Mineralogy is dominated by Fe sulfides nnd amorphous silica. Pyrite, marcasite, wurtzite, chalcopyrite, and iss are the most common sulfide phases. Pyrrhotite, galena, and sphalerite are present in trace amounts. Barite, amorphous silica, and chalcedony are the only non-sulfide phases; anhydrite is not observed in any of the dredge samples, although it is common in the chimney-like samples recovered by “Alvin”.Specific mineralogical-textural zones within the dredge samples are anaoogous to individual layers in East Pacific Rise at 21°N and southern Juan de Fuca Ridge samples, with two exceptions: a coarse-grained, highly porous Fe sulfide-rich interior containing sulfidized tubeworm casts, and a 2–5 cm thick zone near the outer margin of the samples dominated by late stage amorphous silica. The porous interior may have formed by dendritic crystal growth from a slowly circulating fluid within a large enclosed chamber. The amorphous silica deposited from a seawater/hydrothermal fluid mixture percolating slowly through the walls of the enclosed chamber; conductive cooling of the fluid as it traversed the walls allowed amorphous silica to precipitate. These silica-rich zones are the densest, most durable portions of the structures and may be responsible for the lasting stability of the large sulfide features.Observations in these samples are consistent with two distinct phases of development. Phase 1 is analogous to chimney growth and construction at 21°N and ends when flow channels become sealed to rapid flow of through-going fluid. The flow is evidently redirected within the structure. Phase 2 includes dissolution of anhydrite and precipitation of amorphous silica during conductive cooling of sluggishly circulating hydrothermal fluid or seawater/hydrothermal fluid mixtures. Evolution of vent structures through phase 2 allows lateral and vertical growth of unusually large structures.     

Hot spring deposits on the East Pacific Rise at 21°N: preliminary description of mineralogy and genesis

Hydrothermal sulfide-sulfate deposits were sampled from eight active and inactive vent sites along the East Pacific Rise at 21°N during the RISE expedition of April, 1979. The mineralogy of the samples has been determined by X-ray diffractometry, scanning electron microscopy, and X-ray energy dispersive analysis. Mounds of Zn, Fe, and Cu sulfides, dominated by sphalerite, pyrite, and lesser chalcopyrite, are topped by inactive and active chimneys, spouting fluids ≤350°C. The outer zones of active chimneys bear abundant anhydrite precipitated from heated ambient seawater, in addition to hydrothermal pyrite and sphalerite. Mg-hydroxysulfate-hydrate, a phase identified in seawater heating experiments, but previously not observed in nature, is intimately intergrown with anhydrite. Hottest chimneys contain massive chalcopyrite±bornite in their interior zones and belch fluids blackened by a presumably non-equilibrium assemblage of pyrrhotite plus minor sphalerite and pyrite. The early, outer walls of chimneys form from sulfates and the sulfide minerals in black smoke, but metastable pyrrhotite in outer zones is rapidly recrystallized to pyrite or marcasite. Reduction in the permeability of the outer walls permits a high-temperature (>～250°C), low-pH environment within chimneys that enhances precipitation of Cu-Fe sulfides in the central zones. Cooler, worm-covered chimneys emit white fluids bearing particulates of amorphous silica, barite, and pyrite. Amorphous silica and barite are also widely associated with fossilized worm-tubes. Two inactive chimneys are filled with sphalerite, wurtzite, sulfur, pyrite, and marcasite. Anhydrite has been dissolved from these dead chimneys, and the sulfate assemblage is dominated by barite and alteration products such as jarosite and natrojarosite. Silicates other than amorphous silica are not abundant in these deposits, although talc forms in hot chimneys from seawater Mg and hydrothermal silica, and nontronite is found in sediments on the crest of the East Pacific Rise. Other accessory phases identified include copper-rich sulfides such as cubanite, chalcocite, covellite, and digenite; galena; Fe-oxyhydroxides, including goethite; and gypsum. Chimney debris accumulates to form basal mounds, and the mineralogical differences between mounds and chimneys are attributable to weathering of mounds. Mn-oxyhydroxides form crusts within a few meters of the vents, but are not coprecipitating with the sulfide/sulfate minerals.     

Geochemical anomalies of hydrothermal plume at EPR 13°N

During the DY105-12, 14cruise (R/V DAYANG YIHAO, November 2003) on East Pacific Rise (EPR) 12- 13°N, the submarine hydrothermal activity was investigated and the CTD hydrocast was carried out at EPR12°39′N-12°54′N. From the temperature anomalies and the concentrations of magnesium, chlorine, bromine in seawater samples, we discover that magnesium depletes 9.3%-22.4%, chlorine and bro- mine enrich 10.3%-28.7% and 10.7%-29.0% respectively relative to normal seawater at the stations which have chemistry anomalies, moreover temperature and chemistry anomalies are at the same layer. The depletion of magnesium in the plume may be caused by a fluid lacking of magnesium which rises after the hydrothermal fluid reaches the equilibrium with ambient seawater, the enrichment of chlorine and bromine might be the result of inputting later brine which is generated by phase separation due to hydrothermal activity. In addition, the Br/Cl ratio in the abnormal layers at the survey area is identical to that in seawater, which implies that halite dissolution (or precipitation) occurs neither when the fluid is vented nor when hydrothermal fluid entraining ambient seawater rises to form plume. From the ab- normal instance at E55 station, it is very possible that there might exist a new hydrothermal vent site.     

The mineralogy and the isotopic composition of sulfur in hydrothermal sulfide/sulfate deposits on the East Pacific Rise, 21°N latitude

The mineralogy of five groups of hydrothermal chimneys from the East Pacific Rise has been examined. Three of the chimneys, where the exit temperature of the hydrothermal fluids was close to 350°C, are rich in copper sulfides. Exit temperatures from the other two chimneys were less than 300°C; in these, the chimney walls are rich in zinc sulfide. The major sulfides in the chimneys as a whole were found to be wurtzite, chalcopyrite, pyrite, and cubanite. Anhydrite is always the dominant sulfate, and is present in all the deposits. Silicates are also present but in relatively minor amounts. There are considerable differences in the mineralogy of sulfides, sulfates, and silicates between the active and inactive vent deposits.The isotopic composition of sulfur in anhydrites from active vents is close to that of seawater; the δ³⁴S values of the sulfides range from +1.3 to +4.1‰. The isotopic composition of sulfur in the anhydrites is consistent with a derivation predominantly from seawater sulfate. The sulfur in the sulfides must have a complex origin including contributions from both sulfur in basalts and sulfide produced by reduction of sulfate in seawater. Mixing of H₂S-dominated hydrothermal fluids with cold seawater near the seafloor resulted in the precipitation of non-equilibrium assemblages of sulfides and sulfates.     

Ore-forming mechanism for the Xiaoxinancha Au-rich Cu deposit in Yanbian,Jilin Province,China: Evidence from noble gas isotope geochemistry of fluid inclusions in minerals

The Xiaoxinancha Au-rich copper deposit is one of important Au-Cu deposits along the continental margin in Eastern China. The deposit consists of two sections: the Beishan mine (North), composed of altered rocks with veinlet-dissemination sulfides and melnicovite-dominated sulfide-quartz veins, and the Nanshan mine (South), composed of pyrrhotite-dominated sulfide-quartz veins and pure sulfide veins. The isotope compositions of noble gases extracted from fluid inclusions in ore minerals, i.e. ratios of 3He/4He, 20Ne/22Ne and40Ar/36Ar are in the ranges of 4.45―0.08 Ra, 10.2―8.8 and 306―430, respectively. Fluid inclusions in minerals from the Nanshan mine have higher 3He/4He and 20Ne/22Ne ratios whereas those from the Beishan mine have lower 3He/4He ratios. The analysis of origin, and evolution of the ore fluids and its relations with the ore-forming stages and the ages of mineralization suggests that the initial hydrothermal fluids probably come from the melts generated by partial melting of oceanic crust with the participation of fluids from the mantle (mantle-plume type)/aesthenosphere. This also corresponds to the continental margin settings during the subduction of Izanagi ocaneic plate towards the palaeo-Asian continent (123―102 Ma). The veinlet-dissemination ore bodies of the Beishan mine were formed through replacement and crystallization of the mixed fluids generated by mixing of the ascending high-temperature boiling fluid with young crustal fluid whereas the melnicovite-dominated sulfide-quartz veins were formed subsequently by filling of the high-temperature ore fluid in fissures. Pyrrhotite-dominated sulfide-quartz veins in the Nanshan mine were formed by filling-deposition-crystallization of the moderate-temperature ore fluids and the pure sulfide veins were formed later by filling-deposition-crystallization of ore substance-rich fluids after boiling of the moderate-temperature ore fluids. The metallogenic dynamic processes can be summarized as: (1) formation of fluidand ore substance-bearing Adakitic magma by degassing, dewatering and partial melting during subduction of the Izanagi plate; (2) separation and formation of ore fluids from the Adakitic magma; and (3) success-sive ascending of the ore fluids and final formation of the Au-rich Cu deposit of veinlet-dissemination and vein types by secondary boiling.     

The geochemical controls on vent fluids from the Lucky Strike vent field, Mid-Atlantic Ridge

Hydrothermal vent fluids were collected from the Lucky Strike site at 37°17′N on the Mid-Atlantic Ridge in both 1993 and 1996. Seven vents were sampled with the DSV Alvin in 1993 and six vents were sampled in 1996 using the ROV Jason during the LUSTRE '96 Cruise. As three of the vents were sampled in both 1993 and in 1996, a time series of vent fluid chemistry is also reported. Measured temperatures ranged from 202 to 333°C at the 1618–1726 m depth of the vent field, which is located on Lucky Strike Seamount. These fluids are either equal to or less than the local bottom seawater in chlorinity. While the range in fluid compositions at Lucky Strike is generally within that observed elsewhere, the unusual aspects of the fluid chemistries are the relatively high pH and low Fe, Mn, Li and Zn. We attribute this, as well as an usually low Sr/Ca ratio, to reaction with a highly altered substrate. The high Si and Cu contents suggest a deep, as well as hot, source for these fluids. The fluid compositions therefore suggest formation by super-critical phase separation at a depth not less than 1300 m below the seafloor, and reaction with a relatively oxic, and previously altered, substrate. There is temporal variability in some of the vent fluid compositions as Li, K, Ca and Fe concentrations have increased in some of the vents, as has the Fe/Mn (molar) ratio, although the chlorinities have remained essentially constant from 1993 to 1996. While there is not a simple relationship between vent fluid compositions (or temperatures) and distance from the lava lake at the summit of the seamount, the vent fluids from many of the vents can be shown to be related to others, often at distances >200 m. The most southeasterly vents (Eiffel Tower and the Marker/Mounds vents) are distinct in chlorinity and other chemical parameters from the rest of the vents, although closely related to each other within the southeastern area. Similarly all of the vents not in this one area, appear closely related to each other. This suggests one or two source fluids for many of the vents, as is also inferred to be the case at TAG, but which is in contrast to observations on faster spreading ridges. This may suggest inherently different plumbing for hydrothermal systems at slower versus faster spreading ridges.     

Temperature, density and buoyancy fluxes in “black smoker” plumes, and the criterion for buoyancy reversal

Measurements of the temperature and composition of effluent from vents on the sea floor can be used to deduce the in-situ density of this fluid, which is required for calculations of flow in the chimneys and through their porous walls. This density is, however, not directly relevant when calculating the buoyancy flux in the plume above a smoker. It is the asymptotic buoyancy flux, following extensive dilution with seawater, which is required when estimating the height of rise of plumes in a stably stratified ocean, and when calculating the criterion for reversal of buoyancy due to non-linear mixing effects. The results of mixing calculations show that the effluent from hydrothermal vents on the sea floor will exhibit reversing buoyancy if the ejected fluid has a temperature of 300°C and a salinity greater than 8 wt.% NaCl. If the temperature of the effluent is 200°C the salinity required for reversing buoyancy falls to 5.5 wt.% NaCl. Measurements of temperature and salinities of sea-floor hydrothermal fluid suggest that fluids with the characteristics required to form reversing plumes are ejected at the sea floor. The possibility that reversing plumes may be found has important implications for the formation of massive sulfide deposits.     

Fluxes of fluid and heat from the oceanic crustal reservoir

Recent discoveries define a global scale fluid reservoir residing within the uppermost igneous oceanic crust, a region of seafloor that is both warm and may harbor a substantial biosphere. This hydrothermal fluid reservoir formed initially within volcanic rocks newly erupted at mid-ocean ridges, but extends to the vastly larger and older ridge flanks. Upper oceanic crust is porous and permeable due to the presence of lava drainbacks, fissuring, and inter-unit voids, and this porosity and permeability allows active fluid circulation to advect measurable quantities of lithospheric heat from the crust to an average age of 65 Myr. A compilation of crustal porosities shows that this fluid reservoir contains nearly 2% of the total volume of global seawater. Heat flow and sediment thickness data allow calculation of reservoir temperatures, predicting 40°C mean temperatures in Cretaceous crust. Utilizing these temperature estimates, heat flow measurements and models for the thermal structure and evolution of the oceanic lithosphere, we have computed mean hydrothermal fluxes into the deep ocean as a function of plate age. The total hydrothermal volume flux into the oceans approaches 20% of the total riverine input and may contribute to the global seawater mass balance.     

Geothermal constraints on the hydrological regime of the TAG active hydrothermal mound, inferred from long-term monitoring

During August 1994 to March 1995, a period that included ODP Leg 158 drilling, bottom-water and sub-bottom temperatures were continuously logged by a long-term temperature monitoring system ‘Daibutsu’ at the base of the central black-smoker complex (CBC) and within the low heat flow zone at the TAG hydrothermal mound on the Mid-Atlantic Ridge. The temperature of hydrothermal fluid at CBC was also measured with a small high-temperature probe ‘Hobo’. Bottom-water temperature variations measured with Daibutsu at both sites have predominant semi-diurnal periods, causing the sub-bottom temperatures to fluctuate at these periods with reduced amplitudes and phase delays at sub-bottom depths. Seawater entrainment into the mound has been previously suggested at the low heat flow zone. We quantitatively evaluate the seawater entrainment rate at both sites from a one-dimensional numerical model, combined with a heat conduction model for the semi-diurnal variations. The entrainment rate of seawater at the base of CBC is estimated as 1.3±0.5×10⁻⁵ m/s, at least from August 17 to 30, 1994. On the other hand, the seawater entrainment rate at the low heat flow zone was undetected by long-term temperature monitoring at shallow sub-bottom depth. Nevertheless an increase in heat flow observed at the low heat flow zone during ODP drilling can be interpreted as a decrease in the entrainment rate of seawater. Before ODP Leg 158, Daibutsu measured three sub-bottom temperature anomalies at the base of CBC not derived from bottom-water temperature variations and Hobo also detected a CBC fluid temperature anomaly, indicating some natural changes in fluid flow within the mound. Daibutsu and Hobo also measured temperature anomalies during and after drilling at the ODP TAG-1 area. The Hobo temperature anomalies are inferred to have occurred when the cold fluid entrained through the drill holes at TAG-1 site reached or cooled the main fluid path to CBC. The entrained seawater through the drill holes appears to have contributed to dissolution and precipitation of anhydrite within the mound and perhaps affected the local permeability structure inside the mound. The temperature anomalies measured with Daibutsu at the base of CBC may have been induced by the change in the fluid flow pattern as a result of such permeability changes within the mound.     

Geochemistry of ore-forming fluids and geological significance of the Kuoerzhenkuola gold field in Xinjiang, China

The Kuoerzhenkuola gold field (including the Kuo- erzhenkuola and the Buerkesidai gold deposits), lo- cated 68 km east of Jimunai County in northern Xing- jiang, China, is an important component of the Sawuer gold belt which is the eastward extending part of the Zarma-Sawur gold-copper belt in Kazakhstan. Some studies are concerned with the geology of the gold ores[1―3], the associated volcanic rocks[4], radiogenic isotope[5―8], and the ore-forming environment[8]. Most researchers inferr…     

Metallogenic geodynamic background of Mesozoic gold deposits in granite-greenstone terrains of North China Craton

The spatial distribution map of 65 mid-large gold-deposits hosted in the granite-greenstone terrains of the North China Craton is first drawn. These gold deposits mainly concentrate in the Mesozoic remobilized Yinshan-Yan-shan-Liaoning-Jilin intracontinental collisional orogenic belt, the northern Qinling and the Jiaodong Mesozoic collisional orogenic belts, and the Mesozoic intracontinental fault-magmatic belts developed along the Taihangshan and the Tan-Lu faults; their mineralizing time is predominantly Jurassic-Cretaceous, i. e. the Yanshanian. The metallogenic geodynamic background is exactly the compression-to-extension transition regime during continental collision. The results are partly from the project entitled “The main types of gold mineralizations in China and their metallogenic model” (89-El) supported by the Ministry of Metallurgical Industry of China, and projects “Geology and metallogenesis of the main type gold deposits in East Chinaⁿ” (Grant No. 9488010) and “Study on ore-forming fluids of the Wangfeng gold deposit, Xinjiang” supported by the National Natural Science Foundation of China (Grant No. 49672119).     

87Sr/86Sr ratios in hydrothermal waters and deposits from the East Pacific Rise at 21°N

⁸⁷Sr/⁸⁶Sr ratios of three hydrothermal waters collected on the East Pacific Rise at 21°N define a mixing line between seawater and a hydrothermal end-member at 0.7030 which is derived by seawater-basalt interaction at ca. 350°C and water/rock ratio of about 1.5. Sr concentrations are not affected in the process while Mg uptake from seawater is almost complete. Up to2/3 of this hydrothermal component is involved in anhydrite precipitation while the Sr isotopic ratio in sulfides (chalcopyrite + sphalerite) cannot be distinguished from that of sulfate. It is estimated that ca. 1 × 10¹⁰ moles of strontium are yearly cycled in the hydrothermal systems of mid-oceanic ridges, thereby affecting the⁸⁷Sr/⁸⁶Sr budget of seawater. Mass balance between river runoff, limestone precipitation and ridge basalt alteration suggests that the⁸⁷Sr/⁸⁶Sr ratios of the river runoff are in the range 0.7097–0.7113, and are largely dominated by limestone alteration.     

Element enrichment and U-series isotopic characteristics of the hydrothermal sulfides at Jade site in the Okinawa Trough

The geochemical and U-series isotopic characteristics of hydrothermal sulfide samples from the Jade site (127°04.5′E, 27°15′N, water depth 1300–1450 m) at Jade site in the Okinawa Trough were analyzed. In the hydrothermal sulfide samples bearing sulfate (samples HOK1 and HOK2), the LREEs are relatively enriched. All the hydrothermal sulfide samples except HOK1 belong to Zn-rich hydrothermal sulfide. In comparison with Zn-rich hydrothermal sulfides from other fields, the contents of Zn, Pb, Ag, Cd, Au and Hg are higher, the contents of Fe, Al, Cr, Co, Ni, Sr, Te, Cs, Ti and U lower, and the ²¹⁰Pb radioactivity ratios and ²¹⁰Pb/Pb ratios very low. In the hydrothermal sulfide mainly composed of sphalerite, the correlations between rare elements Hf and U, and Hf and Mn as well as that between dispersive elements Ga and Zn, are strongly positive; also the contents of Au and Ag are related to Fe-sulfide, because the low temperature promotes enrichment of Au and Ag. Meanwhile, the positive correlations between Fe and Bi and between Zn and Cd are not affected by the change of mineral assemblage. Based on the ²¹⁰Pb/Pb ratios of hydrothermal sulfide samples (3.99×10⁻⁵-5.42×10⁻⁵), their U isotopic composition (²³⁸U content 1.15–2.53 ppm, ²³⁸U activity 1.07–1.87 dpm/g, ²³⁴U activity 1.15–2.09 dpm/g and ²³⁴U/²³⁸U ratio 1.07–1.14) and their ²³²Th and ²³⁰Th contents are at base level, and the chronological age of hydrothermal sulfide at Jade site in the Okinawa Trough is between 200 and 2000 yr. Supported by the Pilot Project of Knowledge Innovation Project, Chinese Academy of Sciences (Grant No. KZCX2-YW-211), National Natural Science Foundation of China (Grant Nos. 40830849, 40176020), and Special Foundation for the Eleventh Five Plan of COMRA (Grant No. DYXM-115-02-1-03)     

Late Mesozoic subduction‐induced hydrothermal gold deposits along the eastern Asian and northern Californian margins: Oceanic versus continental lithospheric underflow

During late Mesozoic subduction of paleo‐Pacific lithospheric plates, numerous gold vein deposits formed in the Dabie–Sulu Belt of east‐central China plus its east‐Asian extensions, and in the Klamath Mountains plus Sierran Foothills of northern California. In eastern Asia, earlier transpression and continental collision at about 305–210 Ma generated a high pressure–ultrahigh pressure orogen, but failed to produce widespread intermediate to felsic magmatism or abundant hydrothermal gold deposits. Similarly in northern California, strike‐slip ± minor transtension–transpression over the interval of about 380–160 Ma resulted in the episodic stranding of oceanic terranes, but generated few granitoid magmas or Au ore bodies. However, for both continental margin realms, nearly head‐on Cretaceous destruction of oceanic lithosphere involved sustained underflow; reaching magmagenic depths of about 100 km, the descending mafic‐ultramafic plates dewatered, producing voluminous calc‐alkaline arc magmas. Ascent of these plutons into the middle and upper crust released CO₂ ± S‐bearing aqueous fluids and/or devolatilized the contact‐metamorphosed wall rocks. Such hydrothermal fluids transported gold along fractures and fault zones, precipitating it locally in response to cooling, fluid mixing, and/or reactions with wall rocks of contrasting compositions (e.g. serpentinite, marble). In contrast, where sialic crust was subducted to depths of about 100 km, only minor production of granitoid melts occurred, and few major coeval Au vein deposits formed. The mobilization of precious metal‐bearing fluids in continental margin and island arc environments apparently requires long‐continued, nearly orthogonal descent of oceanic, not continental, lithosphere.     

Sources and genesis of the Chinkuashih Au-Cu deposits in northern Taiwan: constraints from Os and Sr isotopic compositions of sulfides

The Chinkuashih district at northern Taiwan hosts one of the largest Au deposits in the western Pacific gold province. Gold were precipitated from hydrothermal solutions as native gold or incorporated into sulfides at a temperature range of 200-350 °C. The sulfides in ore mines have ¹⁸⁷Os/¹⁸⁸Os ratios varying from 0.139 to 0.249. The positive ¹⁸⁷Os/¹⁸⁸Os-1/Os correlation is consistent with derivation from the hybrid fluids containing various proportions of mantle and crustal components. The crustal component was the meteoric water that had acquired its Sr and Os isotopic signatures from the local sedimentary formations and dacitic intrusions. The mantle component was the magmatic fluid segregated from the dacitic magma by fractional crystallization. Based on the ¹⁸⁷Os/¹⁸⁸Os-1/Os correlation, the hybrid fluids forming the Chinkuashih sulfides contained less than 30% magmatic fluid, except for one sulfide sample from Hsumei, which required >40% magmatic fluid. Compared to meteoric water, the magmatic fluid contained a higher Os content (130 times higher) and was enriched in Os relative to Sr with an Os/Sr ratio two orders higher than that of the crustal fluid. Consequently, the Os budget in the hybrid fluids was controlled by the magmatic fluid, although the meteoric water was volumetrically dominated. If gold and Os behave similarly in chemistry, the Chinkuashih gold deposits are of mantle origin and the area where sulfides with the greatest mantle Os signature may host undiscovered gold deposits. Finally, the ¹⁸⁷Os/¹⁸⁸Os ratios of sulfides show no relationship with the mineral assemblages of sulfides, implying that the sulfide mineral assemblages reflect local surfacial redox conditions rather than the chemical characteristics of parental fluids.     

On the formation of metal-rich deposits at ridge crests

Data from the hot springs at the Galapagos spreading center (T = 3–13°C) show depletions of the exiting waters in Cu, Ni, Cd, Se, Cr and U relative to ambient seawater. Manganese is strongly enriched. Iron shows highly variable behavior between vent fields but is in general low. The data confirm the occurrence of extensive subsurface mixing between the primary high-temperature, acid, reducing hydrothermal fluids and “groundwater”. The composition of the latter is indistinguishable from that of the free water column adjacent to the ridge axis. The final solutions are on the boundary between those forming MnO₂ crusts and those producing iron-manganese rich sediments. The suite of metal rich deposits observed at ridge crests — Mn-O, Fe-Mn-O, Fe-S — can be explained as the manifestation of the degree of subsurface mixing, decreasing from 100 : <1 to <1 : 1 across the series (assuming an end-member temperature of 350°C).