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1.
Helium, neon and argon isotope compositions of fluid inclusions have been measured in massive sulfide samples from the Jade hydrothermal field in the central Okinawa Trough. Fluid-inclusion 3He/4He ratios are between 6.2 and 10. l times the air value (Ra), and with a mean of 7.8Ra, which are consistent with the mid-ocean ridge basalt values [3He/^4He≈(6Ra- 11Ra)]. Values for ^20Ne/^22Ne are from 10.7 to 11.3, which are significantly higher than the atmospheric ratio (9.8). And the fluid-inclusion ^40Ar/^36Ar ratios range from 287 to 334, which are close to the atmosperic values (295.5). These results indicate that the noble gases of trapped hydrothermal fluids in massive sulfides are a mixture of mantle- and seawater-derived components, and the helium of fluid inclusions is mainly from mantle, the nelium and argon isotope compositions are mainly from seawater.  相似文献   

2.
Si-Fe-Mn-oxyhydroxides dredged at the PACMANUS(Papua New Guinea–Australia–Canada–Manus)hydrothermal field, Eastern Manus Basin, have 87Sr/86Sr=0.708 079–0.708 581; εNd=5.149 833–6.534 826;208Pb/204Pb=38.245–38.440; 207Pb/204Pb=15.503–15.560; 206Pb/204Pb=18.682–18.783. 87Sr/86 Sr isotope ratios are relatively homogeneous and close to the value of the surrounding seawater(0.709 16). The content of Sr in the samples contributed by seawater was estimated to be 76.7%–83.1% of total amount. The mixing temperature of hydrothermal fluids and seawater were ranging from 53.2°C to 72.2°C and the hydrothermal activities were unstable when the samples precipitated. The εNd values of all the samples are positive, which differ from the values of ferromanganese nodules(crusts) with hydrogenic origin. Nd was mainly derived from substrate rocks leached by hydrothermal circulation and preserved the hydrothermal signature. Pb isotopic compositions of most samples show minor variability except Sample #9–2 that has relatively high values of Pb isotopes. The Pb may be derived from the Eastern Manus Basin rocks leached by the hydrothermal fluid. The slightly lower 208Pb/204 Pb and207Pb/204 Pb values of the samples indicated that the hydrothermal circulation in PACMANUS was not entire and sufficient, or that hydrothermal circulation had transient changes in the past. Si-Fe-Mn-oxyhydroxides in the samples preserved the heterogeneities of local rocks.  相似文献   

3.
The formation mechanism of the large hydrothermal sulˉde deposit is a complex geological process involving many controlling factors. Mixing between hydrothermal °uid and seawater plays a key role in this process. The results of the Ocean Drilling Program (ODP) indicate that mixing of the evolved seawater and hydrothermal °uid, which is wildly developed within the Trans-Atlantic Geo- Traverse (TAG) hydrothermal deposit, governs the internal structure and chemical compositions of the deposit to great extent. Taking the TAG ˉeld for example, the mixing processes of hydrothermal °uid with the seawater heated to di?erent extent are calculated, so as to discuss the impact of hydrothermal °uid/seawater mixing on the formation process of the sulˉde deposit. The results indicate that: (1) mixing between the heated seawater and hydrothermal °uid derived from the deep deposit is largely responsible for the wild precipitation of anhydrite within the TAG hydrothermal deposit; (2) 330{310 ±C is a special temperature range in the mixing process; (3) the mixing and hydrothermal processes in di?erent zones of the TAG hydrothermal deposit (TAG-1, TAG-2 and TAG-5, etc.) have been discussed based on the simulated results.  相似文献   

4.
The REE compositions of hydrothermal deposits and basalt samples from the Southwest Indian Ridge (SWIR) were determined with ICP-MS.The results show that there are significant differences between different types of samples although all samples show relative LREE enrichment.The contents of REE in hydrothermal sulfides and alterated rocks samples are lower (from 7.036 × 10 6 to 23.660 × 10 6),while those in the white chimney deposits are relatively higher (ranging from 84.496 × 10 6 to 103.511 × 10 6).Both of them are lower than basalts.Chondrite-normalized REE distribution patterns show that sulfides and alterated rocks samples are characterized by significant positive Eu anomalies.On the contrary,white chimney deposits have obvious negative Eu anomalies,which may be caused by abundant calcite existing in the white chimney samples.Both the content and distribution pattern of REE in sulfides suggest that REE most possibly is originally derived from hydrothermal fluids,but influenced by the submarine reducing ore-forming environment,seawater convection,mineral compositions as well as the constraint of mineral crystallizations.  相似文献   

5.
Utilizing Si, Fe and Mn concentrations within the end-member PACMANUS hydrothermal fluid, Si-Fe-MnH_2 O Pourbaix diagrams were constructed at 300°C and 25°C. The Pourbaix diagrams show that the main Si, Fe and Mn oxides species precipitating from the hydrothermal fluid were Si O_2, Fe(OH)_3, Fe_3(OH)_8, Mn_3O_4, and Mn_2O_3 at 25°C. During mixing of hydrothermal fluid with seawater, Si O_2 precipitated earlier than FeMn-oxyhydroxides because of the lower stability boundary. Then Fe(OH)_2 precipitated first, followed by Fe_3(OH)_8 and Fe(OH)_3, and last, small amounts of Mn_3O_4 and Mn_2O_3 precipitated. Fe(OH)_3 was readily deposited in alkaline solution with little influence by Eh. There were many Si-Fe-Mn-concentric particles in the polished sections of the massive precipitates collected from PACMANUS. In the concentric nucleus and ellipsoid, Si oxides precipitated first before the hydrothermal fluid had mixed with seawater. In the concentric nucleus, after the precipitation of Si oxides, the increase of p H and Eh promoted the precipitation of Mn oxides around the Si oxides. In the large ellipsoid, the precipitation of Fe was divided into two periods. In the early period, increase of p H value of hydrothermal fluid produced by low-temperature convection and an input of a small volume of seawater promoted a small amount of Fe(OH)_3 to precipitate in the Si-rich core. In the late period, after complete mixing with seawater and the resultant fluid was close to neutral or slightly alkaline in p H, Fe(OH)_3 was easily precipitated from the solution and distributed around the Si-rich core.  相似文献   

6.
A 43 cm long E271 sediment core collected near the East Pacific Rise(EPR) at 13°N were studied to investigate the origin of smectite for understanding better the geochemical behavior of hydrothermal material after deposition.E271 sediments are typical metalliferous sediments. After removal of organic matter, carbonate, biogenic opal,and Fe-Mn oxide by a series of chemical procedures, clay minerals(2 μm) were investigated by X-ray diffraction,chemical analysis and Si isotope analysis. Due to the influence of seafloor hydrothermal activity and close to continent, the sources of clay minerals are complex. Illite, chlorite and kaolinite are suggested to be transported from either North or Central America by rivers or winds, but smectite is authigenic. It is enriched in iron, and its contents are highest in clay minerals. Data show that smectite is most likely formed by the reaction of hydrothermal Fe-oxyhydroxide with silica and seawater in metalliferous sediments. The Si that participates in this reaction may be derived from siliceous microfossils(diatoms or radiolarians), hydrothermal fluids, or detrital mineral phases. And their δ30 Si values are higher than those of authigenic smectites, which implies that a Si isotope fractionation occurs during the formation because of the selective absorption of light Si isotopes onto Feoxyhydroxides. Sm/Fe mass ratios(a proxy for overall REE/Fe ratio) in E271 clay minerals are lower than those in metalliferous sediments, as well as distal hydrothermal plume particles and terrigenous clay minerals. This result suggests that some REE are lost during the smectite formation, perhaps because their large ionic radii of REE scavenged by Fe-oxyhydroxides preclude substitution in either tetrahedral or octahedral lattice sites of this mineral structure, which decreases the value of metalliferous sediments as a potential resource for REE.  相似文献   

7.
This study reports the occurrence of anhydrite in hydrothermally altered pillow basalt (12°50.55′N, 103°57.62′W, water depth 2 480 m), which may have been produced in the basalt during seawater-basalt interaction in the laboratory. The existence of anhydrite in the altered basalt indicates extensive hightemperature hydrothermal alteration at the surface of seafloor pillow basalt. Microprobe analysis shows significant chemical zoning in the hydrothermally altered pillow basalt, in which Ca, Si and Al contents decrease and P, Fe, Mn, Cr and S contents increase from fresh basalt to altered basalt. The negative correlation between Rb-Sr and Li-Sr, and negative correlation between Li-Ca and Rb-Ca in the high-temperature vent fluids show that these fluids underwent anhydrite precipitation before fluid jetting due to mixing with seawater in the sub-seafloor. Based on these observations, we show that not all Ca in the anhydrite comes from basalt in the reaction zone, and that the basalts on the seafloor or in the upflow zone may also provide Ca for anhydrite.  相似文献   

8.
Hydrothermal materials in deep-sea sediments provide a robust tracer to the localized hydrothermal activity at mid-ocean ridges. Major, trace and rare earth element(REE) data for surface sediments collected from the ultraslow spreading Southwest Indian Ridge are presented to examine the existence of hydrothermal component.Biogenic carbonate oozes dominate all the sediment samples, with CaO content varying from 85.5% to 89.9% on a volatile-free basis. The leaching residue of bulk sediments by ~5% HCl is compositionally comparable to the Upper Continental Crust(UCC) in SiO_2, Al_2O_3, CaO, MgO, alkali elements(Rb, Cs) and high field strength elements(Nb, Ta, Zr, Hf, Ti). These detritus-hosted elements are inferred to be prominently derived from the Australian continent by means of eolian dust, while the contribution of local volcaniclastics is insignificant. In addition, the residual fraction shows a clear enrichment in Fe, Mn, and Ba compared with the UCC. Combining the positive Eu anomaly of residual fraction which is opposed to the UCC but the characteristic of hydrothermal fluids and associated precipitates occurred at mid-ocean ridges, the incorporation of localized hydrothermal component can be constrained. REE mixing calculations indicate that more than half REE within the residual fraction(~55%–60%) are derived from a hydrothermal component, which is inferred to be resulted from a diffuse fluid mineralization. The low-temperature diffuse flow may be widely distributed along the slow-ultraslow spreading ridges where crustal faults and fissures abound, and probably have a great mineralization potential.  相似文献   

9.
Serpentinites, which contain up to 13 wt% of water, are important reservoirs for chemical recycling in subduction zones. In the past two decades, forearc mantle serpentinites were identified in different locations around the world. Here, we present petrology and whole rock chemistry of ultramafic and mafic rocks dredged from the Hahajima Seamount, which is located 24–40 km west to the junction of the Izu-Bonin Trench and the Mariana Trench. Nearly all the collected samples are extensively hydrated, and olivine grains in ultramafic rocks are replaced by serpentine minerals, with only one sample preserving remaining trace of orthopyroxene. Our new results show that the Hahajima serpentinized peridotite samples are all MgO-rich(～42 wt%), but have low contents in Al_2O_3, CaO, rare earth and high field strength elements, which is consistent with the overall depleted character of their mantle protoliths. Model calculations indicate that these Hahajima peridotite samples were derived from 10%–25% partial melting of the presumed fertile mantle source, which is generally lower than those of peridotites from Torishima Forearc Seamount, Conical Seamount and South Chamorro Seamount(mostly25%). All the serpentinites from these four forearc seamounts show strong enrichment in fluid-mobile and lithophile elements(Li, Sr, Pb and U). In details, Hahajima Seamount serpentinites do not have obvious enrichment in Cs and Rb, and display remarkably high abundances of U. These observations indicate that the serpentinization of Hahajima peridotites occurred by addition of seawater or low temperature seawater-derived hydrothermal fluid, without or with little contribution from slab-derived fluids. The geochemical signature of serpentinites from Hahajima Seamount could be interpreted as the result of the combination of extensive partial melting and subsequent percolation of seawater through the mantle wedge.  相似文献   

10.
Eighteen samples of hydrothermal sediments from the Jade hydrothermal field in the central Okinawa Trough have been analyzed. Sulfur isotopic values for 10 sulfide samples vary from 5.2 × 10~(-3) to 7.2× 10(-3), δ~(34)S values for 7 sulfate samples vary from 16.3 × 10~(-3) to 22.3 × 10~(-3), and 1 native sulphur sample has a δ~(34)S value of 8.2× 10~(-3). The major sources of sulfur for hydrothermal sediment are intermediate to acid volcanic rocks and sea water sulfate, and it is possible that the partial sulfur of hydrothermal sediment is from the pelagic sediment by the interaction between hydrothermal fluid and sediment. The reasons of causing the distinct differences in sulfur isotopic values for sulfide samples from hydrothermal sediment ( compared with other hydrothermal fields), are the differences in the sources of sulfur, the magmatic activity and the tectonic evolution in different hydrothermal fields. The sulfur evolution is a long and complex process in the seafloor hydrothermal system  相似文献   

11.
对冲绳海槽Jade热液区块状硫化物中流体包裹体的氦、氖和氩同位素组成进行了测定,流体包裹体的3He/4He比值为(6.2～10.1)Ra,均值为7.8Ra,与大洋中脊玄武岩一致[3He/4He≈(6～11)Ra],20Ne/22Ne比值为10.7～11.3,明显高于大气值(9.8),而40Ar/36Ar比值的变化范围在287～334之间,接近大气值(295.5),这些结果表明,块状硫化物中热液流体捕获的稀有气体是地幔和海水源组分混合的产物,且流体包裹体中的氦主要来自地幔,氖和氩主要来自海水。  相似文献   

12.
At Matienzo (Basque–Cantabrian Basin, northern Spain), a large stratabound HTD body (4 by 2 km2 and 80–400 m thick) delimited by two parallel sinistral strike-slip faults is exposed in Aptian carbonates. The margins of the HTD body are characterised by dolomite “tongues” indicating that some limestone beds were more prone to dolomitisation. However, no clear relationship between HTD occurrence and precursor limestone facies can be established. Massive limestone beds, as found at the top of the HTD body, act as barriers to hydrothermal processes, since no dolomite is present in or above these beds. Three types of dolomites have been differentiated, i.e. 1) matrix, 2) coarse crystalline and 3) zebra dolomite. The distribution of the dolomite types is attributed to ascending fluid flow and changing degree of dolomite oversaturation.The dolomite body was formed by two dolomitisation phases under burial conditions. No indications for a synsedimentary/early diagenetic dolomitisation have been observed. The first dolomitisation phase is characterized by ferroan dolomite and the second by non-ferroan dolomite. The two HTD phases are characterised by depleted δ18O-values (ranging between −10‰ and −16‰ V-PDB), δ13C-values similar to the Aptian–Albian marine signature and homogenisation temperatures of primary fluid inclusions between 120 °C and 150 °C. The dolomitising fluid was enriched in 87Sr compared to Aptian seawater, excluding the latter as an unmodified fluid source for dolomitisation. Microthermometry of primary fluid inclusions indicates that the dolomitising fluid evolved from a moderate saline (9.7 – 14.0 wt% NaCl) to a more saline (10.9 – 21.0 wt% NaCl) H2O–NaCl brine. The dolomitising fluid likely originated from evaporated seawater. Fluid circulation through the dolomitised strata is inferred to have taken place during the tectonically active period of the late Albian throughout which important sinistral-strike slip movements along basement faults occurred.  相似文献   

13.
河口有色溶解有机物（colored dissolved organic matter,CDOM）的分布是各种物理-生物地球化学过程共同作用的结果。为实现河口高动态变化CDOM的监测，遥感是一种重要的手段。由珠江口四个不同季节的航次获得的实测数据，本文构建了一个遥感算法以反演CDOM在400 nm的吸收系数（aCDOM （400））。该算法使用以波段反射率比值Rrs （667）/Rrs （443）和Rrs （748）/Rrs （412）为自变量。将构建的算法应用于2002-2014年的MODIS/Aqua数据，本文计算了珠江口不同季节的aCDOM （400）气候态分布。CDOM的分布主要受珠江径流量和区域水下地形特征的影响。沿着垂直于水深梯度的断面，气候态aCDOM （400）呈指数减少（y=aebx,b<0），但不同季节差异很大。珠江口CDOM主要是河流淡水输运而来。其中，富里酸比例随盐度的增加而降低。基于构建的算法、CDOM保守混合方程和径流量，本文由MODIS/Aqua数据进一步估算了2002-2014年夏季和冬季珠江DOC的有效入海浓度和有效入海通量。珠江的有效入海浓度和有效入海通量都与流量存在正相关关系，且在夏季的相关性更明显，R2分别为0.698和0.9657。  相似文献   

14.
The exceptional development of coeval hydrocarbon and aqueous fluid inclusions (FI) in fluorite from the MVT-type ore deposit of Koh-i-Maran, Baluchistan (North Kirthar range, Pakistan), provides samples which are representative of the ore-forming fluid and which support the hypothesis of petroleum migration in the province. Primary brines at 125°C (10 wt% equ. NaCl) and secondary CH4-rich brines at 135°C (7 wt% equ. NaCl), are recognised to be associated with oil migration in the fluid inclusions. They support the model of a per ascensum MVT (Mississippi Valley Type) stratabound hydrothermal deposit. A pressure–temperature path of 120–125°C to 165–200 bars is calculated from microthermometric data and PVT modelling of hydrocarbon FI using the modified Peng–Robinson Equation of State (IFP software) from primary cogenetic inclusions (oil and brines).The composition of gas and oil fractions is obtained by a combination of Synchrotron FTIR microanalysis and gas chromatography performed on individual fluid inclusions. The oil entrapped as a coeval primary fluid phase is a light aliphatic normal oil in the range C8–C35 with a high CO2 content. The brown solid phase found systematically in the oil is probably asphaltene resulting from precipitation after trapping of the heavy fraction, which commonly occurs by decreasing pressure and temperature and\or by CO2 injection. Later CH4-rich brine influx probably modified part of the oil in the primary fluid inclusions because degraded oil is observed within such inclusions. Biomarkers obtained by GC-MS analysis indicate a terpane distribution quite similar to the nearest oil seepage in the Gokurt area. This result and the high CO2 content of organic fluid inclusions indicate a restricted/confined sedimentary environment for the source rock, which could correspond to the Eocene Carbonate formation with type-II organic matter. A possible additional input of gas from the Sambar formation is suggested as feasible. The link between the fluid inclusion data and the geodynamic evolution lead us to propose a circulation of basinal fluids driven mainly by the fault system during dewatering in the foredeep. In Pakistan, they are coeval to major compressional NW–SE Oligocene episode in the thrust belt. The origin of the fluorine may be found in the basin sediments as well as near the basement. The brines originated in salt structures recognized in eocambrian at the decollement level, the source rock was already mature.  相似文献   

15.
A new, automatic hydrothermal fluid sampler using a shape-memory alloy   总被引：2，自引：0，他引：2  
A new hydrothermal fluid sampler has been developed to provide more maneuverability in underwater operation. The sampler characteristically employs a shape-memory alloy, which senses high temperature and actuates the suction mechanism. A shape-memory alloy is also used to switch the intake valve of the sampler, the intention being to avoid missampling when the inlet is in low temperature water. Prototype samplers were designed to collect the fluids hotter than 80°C. Test sampling was performed at hydrothermal vents (1372–1374 m deep) in the submarine volcano, Suiyo Seamount, Izu-Bonin Arc, northwestern Pacific. Observed fluid temperature was between 138 and 298°C, while the ambient seawater temperature was 3.1°C. Each prototype collected about 100 ml fluid as designed. The magnesium concentration in the samples indicated a seawater content of 47.5–90.8%, which indicates the entrainment of ambient seawater. Microscopic observatinn revealed the occurrence of microorganisms in the sample fluids at a population density of 105 to 106 cells ml−1, which is 2–3 orders of magnitude higher than those in seawater at that depth. The use of the newly developed fluid sampler will greatly facilitate the collection of vent-associated microorganisms, which are of potential biological and biotechnological interest.  相似文献   

16.
海水石油类物质吸收系数遥感化提取算法研究   总被引：2，自引：0，他引：2  
Establishing the remote sensing algorithm of retrieving the absorption coefficient of seawater petroleum substances is an efficient way to improve the accuracy of retrieving a seawater petroleum concentration using a remote sensing technology. A remote sensing reflectance is a basic physical parameter in water color remote sensing. Apply it to directly retrieve the absorption coefficient of seawater petroleum substances is of potential advantage. The absorption coefficient of waters containing petroleum [ACWCP, a_o(λ)], consists of the absorption coefficient of pure water [ACPW, a_w(λ)], plankton [ACP, a_(ph)(λ)], colored scraps [ACCS, a_(d,g)(λ)], and petroleum substance [ACPS, a_(oil)(λ)]. Among those, ACCS consists of the absorption coefficient of nonalgal particle [ACNP, a_d(λ)] and colored dissolved organic matter [ACCDOM, a_g(λ)]. For waters containing petroleum, the retrieved ACCS using the existing method is a combination absorption coefficient of ACNP,ACCDOM and ACPA [CAC, a_(d,g,oil)(λ)]. Therefore, the principle question is how to extract ACPS from CAC.Through the analysis of the three proportion tests conducted between the year of 2013 and 2015 and the corresponding remote sensing data, an algorithm of retrieving the absorption coefficient of petroleum substances is proposed based on remote sensing reflectance. First of all, ACPS and CAC are retrieved from the reflectance using the quasi-analytical algorithm(QAA), with some parameter modified. Secondly, given the fact that the backscatter coefficient [BC, b_(bp)(555)] of total particles at 555 nm can be obtained completely from the reflectance, the relation between BC and ACNP in petroleum contaminated water can be established. As a result, ACNP can be calculated. Then, combining the remote sensing retrieving algorithm of a_g(440), the method of achieving the spectral slope of the absorption coefficient can be established, from which ACCDOM,can be calculated. Finally, ACPS can be computed as the residual. The accuracy of ACPS based on this algorithm is 86% compared with the in situ measurements.  相似文献   

17.
Instead of approximation formula ln(E(t)/E(0)) = [(a ? bt)t/(c + T)] commonly used at present for representing dependence of pressure of saturated streams of liquid water E upon temperature we suggested new approximation formula of greater accuracy in the form ln(E(t)/E(0)) = [(A ? Bt + Ct 2)t/T], where t and T are temperature in °C and K respectively. For this formula with parameters A = 19.846, B = 8.97 × 10?3, C = 1.248 × 10?5 and E(0) = 6.1121 GPa with ITS-90 temperature scale and for temperature range from 0°C to 110°C relative difference of approximation applying six parameter formula by W. Wagner and A. Pruß 2002, developed for positive temperatures, is less than 0.005%, that is approximately 15 times less than accuracy obtained with the firs formula. Increase of temperature range results in relative difference increasing, but for even temperature range from 0°C to 220°C it does not higher than 0.1%. For negative temperatures relative difference between our formula and a formula of D. M. Murphy and T. Koop, 2005, is less than 0.1% for temperatures higher than ?25°C. This paper also presents values of coefficients for approximation of Goff and Grach formula recommended by IMO. The procedure of finding dew point T d for known water steam pressure e n based on our formula adds up to solving an algebraic equation of a third degree, which coefficients are presented in this paper. For simplifying this procedure this paper also includes approximation ratio applying a coefficient A noted above, in the form T d (e n ) = \(\frac{{AT_0 }}{{A - \varepsilon }}\) + 0.0866?2 + 0.0116?10/3, where ? = ln(e n /E(T 0)). Error of dew point recovery in this ratio is less than 0.005 K within the range from 0 to 50°C.  相似文献   

18.
 Hydrothermal vent fields south of the Garret Fracture zone were sampled for the isotope composition of helium and oxygen ([18O]H2O/[16OH2O). The helium isotopes end-member (3He / 4He=8.3×R a and [4He]≈1.2–2.4×10-5 cm3 STP g-1) is quite similar to other known hydrothermal sites pointing to the homogeneous helium composition of the upper mantle. The δ18O end-member value (δ18O≈0.5–0.6‰) confirms previous suggestions from other sites and from isotope modeling, that hydrothermal fluids are slightly enriched in 18O relative to the ocean as a result of water–rock interactions at high temperature. Received: 11 December 1995/Revision received: 20 December 1996  相似文献   

19.
The Dongsha area is one of the most promising target areas for gas hydrate exploration in the South China Sea(SCS).The study of pore water geochemistry has played a key role in Chinese gas hydrate exploration.Br/Cl,I/Cl and δ37Cl in pore water were applied here in tracing gas hydrate occurrence,chemical evolution of pore fluids and water/rock interactions in low temperature sediment environments.The samples were collected from Sites HD255 PC and HD309 PC in the Dongsha area in 2004.At Site HD255 PC,we found the elevated Br/Cl,I/Cl and decreased SO_4/Cl at the depth of 4–5 m,suggestive of a laterally migrated fluid probably generated from the gas hydrate occurrence.The range of δ37Cl is –0.54‰ to +0.96‰,and positive δ~(37)Cl at 4–5 m interval should be related with different diffusion rates between ~(35)Cl and ~(37)Cl.At Site HD309 PC,a laterally migrated fluid was also found at the depth of 3–4 m,with the Br/Cl two times to that of the seawater and decreased I/Cl,indicating the fluid has no relationship with the gas hydrate.In this site,the chlorine isotopic composition varies from –0.7‰ to+1.9‰.Extra high Br/Cl might relate with the deep generated fluid.At higher temperature and pressure,the Br/Cl of the fluid is elevated during the hydrous silicate formation,while positive δ37Cl is also associated with the same mechanism.  相似文献   

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