Zhigang Zeng

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.

Elemental and isotopic compositions of the hydrothermal sulfide on the East Pacific Rise near 13°N

The mineralogical, elemental, and isotopic characteristics of a hydrothermal sulfide sample from one dredge station (12°42.30′N, 103°54.48′W, water depth 2655 m) on the East Pacific Rise near 13°N were analyzed. The hydrothermal sulfide was composed mainly of sphalerite, chalcopyrite, and pyrite and was a Zn-rich sulfide; in layer ep-s-1, goethite formed by secondary oxidation was found. The concentrations of rare elements, such as Li (0.15×10−6–0.30×10−6), Be (0.01×10−6–0.05×10−6), Zr (73.8×10−9–1344×10−9), Nb (8.14×10−9–64.7×10−9), Hf (2.54×10−9–28.0×10−9), and Ta (0.203×10−9–1.21×10−9), were far lower in the hydrothermal sulfide than in the ocean crust, whereas the content of Au was higher and the contents of Co, Ni, Sr, Cs, Ba, Bi, and U were low. The correlations between Zn and Cr, Cd and Ga, Cu and P, P and In (R2 > 0.8) were positive, whereas those between Zn and Fe, Cu, and Ba (R2 > 0.8) were distinctly negative. From low-temperature mineral assemblages to high-temperature mineral assemblages, the spatial distributions of dispersive and rare elements (e.g. In, Li, Cs) in the hydrothermal sulfide displayed corresponding variations. The variations observed in some elements (e.g., Cd, Cs, P) are controlled by Zn, Fe, and Cu sulfides, respectively. Seafloor weathering accounts for the enrichment of V, Mn, and rare earth elements (REE) in the henna sulfide-oxidation layer that bears the secondary oxide mineral, leading to identical REE patterns for this layer (ep-s-1) and seawater. Seafloor weathering also distinctly affects the correlations between the element ratios of the hydrothermal sulfide. From high-temperature mineral assemblages to low-temperature mineral assemblages, Fe content and δ34S value of the hydrothermal sulfide increase gradually, and Zn content and lead isotopic ratios decrease gradually on the contrary, which indicate the influences of seawater on elements and the sulfur and lead isotopic compositions enhance gradually during the formation of hydrothermal sulfides.

Component characteristics of organic matter in hydrothermal barnacle shells from Southwest Indian Ridge

In 2008–2009, hydrothermal barnacle and sediment samples were collected from the Southwest Indian Ridge during a survey of the China Ocean Mineral Resources R&D Association (COMRA). Samples were analyzed by gas chromatography-mass spectrometer (GC-MS), revealing the main organic constituents of hydrothermal barnacle and sediment to be fatty acids and alkylbenzenes. N-alkanes which possessed obvious even carbon advantage were also detected in hydrothermal sediment. The high concentrations of aromatic compounds might be the result of macromolecular thermal alteration. Microorganism in the submarine hydrothermal ecosystem, especially those related to sulfur metabolism, might be the source of the high concentrations of fatty acids detected in these samples. In high temperature and high pressure hydrothermal environments, n-alkanes which possessed obvious even carbon advantage might originate from thermal alteration of carboxylic acids and other lipid compounds.

Factors affecting the rare earth element compositions in massive sulfides from deep-sea hydrothermal systems

To reconstruct the evolution of ore-forming fluids and determine the physicochemical conditions of deposition associated with seafloor massive sulfides, we must better understand the sources of rare earth elements (REEs), the factors that affect the REE abundance in the sulfides, and the REE flux from hydrothermal fluids to the sulfides. Here we examine the REE profiles of 46 massive sulfide samples collected from seven seafloor hydrothermal systems. These profiles feature variable total REE concentrations (37.2-4092 ppb) and REE distribution patterns (La-CN/Lu-CN ratios = 2.00-73.8; (Eu/Eu*) CN ratios = 0.34-7.60). The majority of the REE distribution patterns in the sulfides are similar to those of vent fluids, with the sulfides also exhibiting light REE enrichment. We demonstrate that the variable REE concentrations, Eu anomalies, and fractionation between light REEs and heavy REEs in the sulfides exhibit a relationship with the REE properties of the sulfide-forming fluids and the massive sulfide chemistry. Based on the sulfide REE data, we estimate that modern seafloor sulfide deposits contain approximately 280 t of REEs. According to the flux of hydrothermal fluids at mid-ocean ridges (MORs) and an average REE concentration of 3 ng/g in these fluids, hydrothermal vents at MORs alone transport more REEs (>360 t) to the oceans over the course of just 2 years than the total quantity of REEs in seafloor sulfides. The excess REEs (i.e., the quantity not captured by massive sulfides) may be transported away from the systems and become bound in sulfate deposits and metalliferous sediments.

Magma mixing in upper mantle: Evidence from high Mg# olivine hosted melt inclusions in MORBs near East Pacific Rise 13°N

Early formed high-Mg# olivine phenocrysts during evolution of MORB magmas usually host melt inclusions, which record important information about the early-stage evolution of magma. Five MORB samples from near East Pacific Rise (EPR) 13°N vary little in K/Ti (0.07–0.12), Tb/Lu (1.72–1.84) and Sm/Nd (0.310–0.332) and have similar REEs patterns, indicating that depleted upper mantle has similar mineral composition. Sixty-five initial melt inclusions derived by correcting olivine fractionation and “FeO-Loss” show averagely higher MgO contents than their host rocks. Melt inclusions have higher CaO/Al2O3 ratios than their host rocks, and these CaO/Al2O3 ratios are positively and negatively correlated with MgO and Na2O respectively, suggesting that these magmas have experienced high pressure crystallization of clinopyroxene. Average crystallization pressure, which is calculated based on the pressure dependence of clinopyroxene crystallization, is 0.83±0.25 GPa, and implys that these melt inclusions are averagely trapped in mantle depth of ∼24 km. These melt inclusions show negative correlations of Ca8/Al8 and Na8 with Fe8, and wider ranges of Ca8/Al8, Na8, Fe8 and K/Ti than their host rocks, suggesting that these melt inclusions formed by mixing magmas of different melting degrees and depths. According to the average value and ranges of Ca8/Al8, Na8, Fe8 and K/Ti, these magmas would necessitate other mixing ends in shallow crust except in upper mantle. The compositional diversity of melt inclusions in MORBs phenocrysts cannot always be used to indicate magma mixing and crystallization in shallow crust, and melt inclusions in high Mg# olivine formed under mantle pressure must be excluded in study of the magma process at crustal level. This study shows that, in EPR, MORBs have experienced mixing of magmas formed by different melting degrees and depths in the mantle.

Abundance and distribution of fatty acids in sediments of the South Mid-Atlantic Ridge

Sediment samples obtained from the South Mid-Atlantic Ridge were studies by gas chromatography-mass spectrometer (GC-MS) for the abundance and distributions of total fatty acids (TFAs). Approximately 34 fatty acids were identified, with the chain-lengths ranging from C12 to C30. The total concentrations of TFAs (ΣTFA) ranged from 7.15 to 30.09 μg g−1 dry sediment, and ΣTFA was weakly correlated with bitumen content (R2 = 0.69). The ΣTFA of samples around hydrothermal areas were significantly higher than that of samples away from hydrothermal areas, indicating intense primary production and large biomass in the hydrothermal areas, and suggesting a close relationship between hydrothermal activity and ΣTFA of samples. The characteristics of the TFA composition in the present study are rich in monounsaturated fatty acids and lacking in polyunsaturated fatty acids, and the ratios between the concentrations of monounsaturated fatty acids and ΣTFAs in samples close to the hydrothermal areas, are about 0.8, but for samples far from the hydrothermal areas, they are only about 0.5. Several fatty acids (e.g., a/iC15:0 and C16:1ω7), which are signature biomarkers for sulfur-metabolizing bacteria, show the same distribution trend as ΣTFA of samples, further highlighting the close relationship between fatty acid content and hydrothermal activity and/or hydrothermal communities. The metabolic activities of hydrothermal communities, especially those of microorganisms, are likely the main source of fatty acids in samples.

Geochemical and Sr-Nd-Pb isotopic compositions of volcanic rocks from the Iheya Ridge, the middle Okinawa Trough: implications for petrogenesis and a mantle source

As an active back-arc basin, the Okinawa Trough is located in the southeastern region of the East China Sea shelf and is strongly influenced by the subduction of the Philippine Sea Plate. Major element, trace element and Sr-Nd- Pb isotopic composition data are presented for volcanic rocks from the Iheya Ridge (IR), the middle Okinawa Trough. The IR rocks record large variations in major elements and range from basalts to rhyolites. Similar trace element distribution characteristics together with small variations in 87Sr/86Sr (0.703 862–0.704 884), 144Nd/143Nd (0.512 763–0.512 880) and Pb isotopic ratios, demonstrate that the IR rocks are derived from a similar magma source. The fractional crystallization of olivine, clinopyroxene, plagioclase, and amphibole, as well as accessory minerals, can reasonably explain the compositional variations of these IR rocks. The simulations suggest that approximately 60% and 75% fractionation of an evolved basaltic magma can produce trace element compositions similar to those of the intermediate rocks and acid rocks, respectively. The analysis of their Sr-Nd-Pb isotopic content ratios suggest that the source of the rocks from the IR is close to the depleted mantle (DM) but extends to the enriched mantle (EMII), indicating that the mantle source of these rocks is a mixture between the DM and EMII end members. The simulations show that the source of the IR volcanic rocks can be best interpreted as the result of the mixing of approximately 0.8%–2.0% subduction sediment components and 98.0%–99.2% mantlederived melts.

Characteristics of hydrocarbons in sediment core samples from the northern Okinawa Trough

Sediment core samples from the northern Okinawa Trough (OT) were analyzed to determine abundances and distributions of hydrocarbons by gas chromatography-mass spectrometer (GC-MS). The results show that the n-alkanes in this sediment core conform to a bimodal distribution, and exhibit an odd-to-even predominance of high molecular weights compared to an even-to-odd predominance in low molecular weight n-alkanes with maxima at C16 and C18. The concentrations of bitumen, alkanes and polyaromatic hydrocarbons (PAHs) were higher in samples S10-07 than all others. Three maturity parameters as well as the ratios between parent phenanthrenes (Ps) and methylphenanthrenes (MPs) in samples S10-07 and S10-17 were higher. The distribution and composition of hydrocarbons in sample S10-07 suggest that one, or several, undetected hydrothermal fields may be present in the region of this sediment core. Results also suggest that volcanism may be the main reason for the observed distribution and composition of hydrocarbons in S10-17 sample.

Two-stage Influences of Hydrothermal Fluids on Pumice Near the Iheya North Hydrothermal Field, Okinawa Trough

ABSTRACT Hydrothermal precipitates and hydrothermal alteration products could record important information about temporal variations of seafloor hydrothermal systems. Geochemistry, mineralogy, and microscopic features of three pumice samples (T3-1, T3-2, and T3-3) near the Iheya North hydrothermal field were analyzed in this article. The results show that T3-3 sample has undergone at least two-stage influences by hydrothermal fluids. In the first stage, pure amorphous silica from hydrothermal fluid precipitated in the vesicles of all three T3 samples as a result of conductive cooling and fluid–seawater mixing. The precipitation temperatures according to oxygen isotope thermometer are approximately 13–21°C. In the second stage, T3-3 pumice underwent low-temperature hydrothermal alteration, during which the amorphous silica precipitates were redissolved, together resulting in losses of FeO and SiO2 and gains of MgO, Pb, Zn, and Cu. Furthermore, ferruginous filamentous silica, which might be related to activities of Fe-oxidizing bacteria, was formed in the altered pumice. The transformation from pure amorphous silica precipitation to redissolution of the silica in T3-3 pumice might indicate a rise of temperature and/or decrease in silica concentrations in hydrothermal fluids, implying a changing hydrothermal environment.

Mineral chemistry indicates the petrogenesis of rhyolite from the southwestern Okinawa Trough

To reveal the petrogenesis of rhyolite from the southwestern Okinawa Trough, the mineral chemistry of plagioclase, orthopyroxene, amphibole, quartz and Fe-Ti oxide phenocrysts were analyzed using an electron microprobe, and in suit Sr and Ba contents of plagioclase analysed by LA-ICPMS were chosen for fingerprinting plagioclases of different provenances. Results indicate an overall homogeneous composition for each of the mineral phases except for plagioclase phenocrysts which have a wide range of composition (An=39~88). Plagioclase crystals characterized by An contents of >70 are not in equilibrium with their whole-rock compositions, and coarse-sieved plagioclase phenocryst interiors record high An contents (>70) and Sr/Ba ratios (>7), which are similar to the those of plagioclase crystals in basalt. Therefore, these crystals must have been introduced to the rhyolitic magma from a more mafic source. Equilibrium temperatures estimated using orthopyroxene-liquid, iron–titanium oxide, titanium-in-quartz and amphibole geothermometers show consistent values ranging from 792 to 869°C. The equilibrium pressure calculated using amphibole compositions is close to 121 MPa which corresponds to an approximate depth of 4 km. The fO2 conditions estimated from Fe-Ti oxides and amphiboles plot slightly above the NNO buffer, which indicates that the rock formed under more oxidized conditions. Our results suggests that petrogenesis of the rhyolite due to basaltic magma ascend with the high An and Sr/Ba plaigoclases from deep magma chamber into the shallow chamber where the fractional crystallization and crustal assimilation happened. It also indicates that a two-layer magma chamber structure may occur under the southwestern Okinawa Trough.