Origin of waters responsible for serpentinization of the Izu-Ogasawara-Mariana forearc seamounts in view of hydrogen and oxygen isotope ratios

Many serpentinite seamounts occur over a region 20–120 km west of the trench axis in the Izu-Ogasawara-Mariana forearc regions. The hydrogen and oxygen isotopic compositions of serpentine from these regions indicate that there are at least two kinds of waters responsible for serpentinization: seawater and water derived from dehydration of the descending slab. Serpentine from two Mariana and two Torishima samples with microscopically ductile and sheared texture (sheared-type) have lowerδD(−63to−52‰) and slightly higherδ18O values (+6.1 to +8.2‰) than that of other nine Ogasawara samples with mesh texture (mesh-type) (δD= −43to−49‰ andδ¹⁸O= +5.8to+6.7‰). This suggests that the sheared-type serpentine with lowerδD and slightly higherδ¹⁸O values was formed within the wedge mantle by interaction with water derived from a descending slab. The sheared texture is likely to have been produced during diapiric uplift. The unaltered portion of the ultramafic bodies later interacted with seawater after emplacement at or near the seafloor, resulting in formation of the mesh-type serpentine with higherδD values.     

Use of oxygen isotope ratios in correlation of tuffs,East Rudolf Basin,northern Kenya

Oxygen isotope determinations were made using CoF₃ to extract oxygen from 27 volcanic glass samples from the East Rudolf Basin, northern Kenya. Results show that the older tuffs are progressively enriched in¹⁸O and that this index can be used in the correlation of volcanic ash units. This method could not distinguish individual samples from the youngest units studied because their ranges of δ¹⁸O overlap. The δ¹⁸O values for the shards in the Tulu Bor Tuff, the KBS Tuff, the Koobi Fora Tuff and the Chari Tuff range from 14.5 to 16.4, from 8.9 to 9.5, from 6.6 to 7.0 and from 7.0 to 7.2, respectively, in decreasing age. Determinations from pumice cobbles are consistently higher than the above values.     

An oxygen isotope study of hydrothermal alteration in the Lake City caldera, San Juan Mountains, Colorado

A 23-m.y.-old, fossil meteoric-hydrothermal system in the Lake City caldera (11 × 14 km) has been mapped out by measuring δ ¹⁸O values of 300 rock and mineral samples. δ ¹⁸O varies systematically throughout the caldera, reaching values as low as −2. Great topographic relief, regional tilting, and variable degrees of erosion within the caldera all combine to give us a very complete section through the hydrothermal system, from the surface down to a depth of more than 2000 m. The initial δ ¹⁸O value of the caldera-fill Sunshine Peak Tuff was very uniform (+7.2 ± 0.1), making it easy to determine the exact amount of ¹⁸O depletion experienced by each sample during hydrothermal alteration. Also, we have excellent stratigraphic control on depths beneath the mid-Tertiary surface, quantitative information on mineralogical alteration products, and accurate data on the shape of the central resurgent intrusion, which was the principal ‘heat engine’ that drove the hydrothermal circulation. Major conclusions are: (1) Although pristine mid-Tertiary meteoric waters in this area had δ ¹⁸O −14, these fluids were ¹⁸O-shifted upward to about δ¹⁸O = −8 to −5 prior to entering the shallow convective system associated with the resurgent intrusive rocks. Although there was undoubtedly radial inflow toward the caldera from all directions, the highly fractured Eureka Graben, southwest of the caldera, was probably the principal source of recharge groundwater for the Lake City system. (2) Fluid flow within the caldera was dominated by three major categories of permeable zones: the porous megabreccia units (which dip outward from the resurgent dome), vertical fractures and faults related to resurgence, and the caldera ring fault itself. All of these zones exhibit marked ¹⁸O depletions, and they are also typically intensely mineralogically altered. (3) The resurgent intrusive stock and its contact metamorphic aureole of hornfels both experienced water/rock ratios lower than the permeable zones; however, they have similarly low δ ¹⁸O values because they were altered at higher temperatures. (4) Throughout the caldera, the δ ¹⁸O of Sunshine Peak Tuff decreases with increasing depth (about 6 per mil/km), indicative of a shallow thermal gradient, typical of a convective hydrothermal system. The near-surface portion of this gradient was controlled by the temperature drop associated with boiling in the uprising fluid. (5) Deeply circulating meteoric water rose along permeable ring fractures 3 to 5 km beneath the mid-Tertiary surface. These fluids were drawn into the shallow convective system through the lower, porous, megabreccia units. Near the resurgent intrusions, fluid flow was again directed upward where resurgence-related, near-vertical fractures intersect the megabreccia units.     

Hydrogen and oxygen isotope studies of metamorphic fluid-rock interactions in the Dabie Mountains

Hydrogen and oxygen isotope studies were carried out on mineral separates from high to ultrahigh pressure metamorphic rocks at Huangzhen and Shuanghe in the eastern Dabie Mountains, East China. The δ¹⁸O values of eclogites cover a wide range of −5‰ to+9‰, but the δD values of micas fall within a narrow range of −85% to −70‰. Both equilibrium and disequilibrium oxygen isotope fractionations were observed between quartz and the other minerals, with reversed fractionations between omphacite and garnet in some eclogite samples. The δ¹⁸ O values of −5‰ to −1‰ for some of the eclogites represent the oxygen isotope compositions of their protoliths which underwent meteoric water-rock interaction prior to plate subduction. The preservation of oxygen isotope heterogeneity in the eclogites implies a channelized flow of fluids during progressive metamorphism caused by rapid subduction. Retrograde metamorphism has caused oxygen and hydrogen isotope disequilibria between some of the minerals, but the fluid for retrograde reactions was internally buffered in the stable isotope compositions. Project supported by the Chinese Ministry of Science and Technology (Grant No. 95-Pre-39), the National Natural Science Foundation of China (Grant Nos. 49794042, 49473173 and 49453003) and the Chinese Academy of Sciences (Grant No. KZ951-A1-401-5)     

Hydrogen and oxygen isotopic compositions of waters from fumaroles at Kilauea summit,Hawaii

Condensate samples were collected in 1992 from a high-temperature (300° C) fumarole on the floor of the Halemaumau Pit Crater at Kilauea. The emergence about two years earlier of such a hot fumarole was unprecedented at such a central location at Kilauea. The condensates have hydrogen and oxygen isotopic compositions which indicate that the waters emitted by the fumarole are composed largely of meteoric water, that any magmatic water component must be minor, and that the precipitation that was the original source to the fumarole fell on a recharge area on the slopes of Mauna Loa Volcano to the west. However, the fumarole has no tritium, indicating that it taps a source of water that has been isolated from atmospheric water for at least 40 years. It is noteworthy, considering the unstable tectonic environment and abundant local rainfall of the Kilauea and Mauna Loa regions, that waters which are sources to the hot fumarole remain uncontaminated from atmospheric sources over such long times and long transport distances. As for the common, boiling point fumaroles of the Kilauea summit region, their ¹⁸O, D and tritium concentrations indicate that they are dominated by recycling of present day meteoric water. Though the waters of both hot and boiling point fumaroles have dominantly meteoric sources, they seem to be from separate hydrological regimes. Large concentrations of halogens and sulfur species in the condensates, together with the location at the center of the Kilauea summit region and the high temperature, initially suggested that much of the total mass of the emissions of the hot fumarole, including the H₂O, might have come directly from a magma body. The results of the present study indicate that it is unreliable to infer a magmatic origin of volcanic waters based solely on halogen or sulfur contents, or other aspects of chemical composition of total condensates.     

基于氢氧同位素分析南昌地震台流体观测井水补给来源

在地震地下流体研究中,地下水补给及循环过程是重要的研究内容之一,氢氧同位素示踪技术是目前研究该过程的常用手段。南昌地震台流体观测井自2013年8月22日投入观测以来,其基础数据未进行有效分析,通过对南昌井水样数据进行氢氧同位素及水化学实验分析,结果表明：井水主要补给源为直接大气降雨,补给前经历了一定蒸发作用;水—岩反应不充分,属于未成熟水;水样中无明显优势阳离子,Ca²⁺、Na⁺占主体,优势阴离子为HCO₃^－,表明井水属重碳酸型水;水源补给高程约582 m。南昌地震台流体观测井总体受大气降水影响较大。     

Carbon isotope ratios of C_4 plants in loess areas of North China

Recent stable carbon isotope studies have shown that the occurrence of C4 plants on the Earth was much later than that of C3 plants and there was a global ex-pansion of C4 biomass around 5―8 million years ago[1]. Although far fewer species use the C4 pat…     

Hydrogen and oxygen isotope compositions of eclogites from the Dabie Mountains and geodynamic implications

Heterogeneous δ¹⁸O values as low as - 2.6‰ to+7.0% are observed for ultrahigh pressure eclogites from the Dabie Mountains in East China. Oxygen isotope equilibrium has been approached between the eclogite minerals, suggesting that the rocks would have acquired the unusual δ¹⁸O values prior to ultrahigh pressure metamorphism by interaction with¹⁸O-depleted fluid. δD values of hydroxyl-bearing are between — 51% and - 83‰, precluding the possibility of paleoseawater involvement. The only likely fluid is ancient meteoric water that exchanged oxygen isotopes with the eclogite precursor (a kind of basaltic rocks) formerly resident on the continental crust. This suggests a crustal recycling process in the suture zone of late subduction. Because silicate minerals undergo rapid oxygen isotope exchange at mantle pressures, preservation of the isotopic signature of meteoric water in the eclogites indicates limited crust-mantle interaction and thus a short residence time (<20 Ma) when the plate containing the eclogite precursor was subducted to mantle depths. The agreement in oxygen isotope temperatures for different mineral pairs suggests a rapid cooling and ascent process for the eclogites subsequent to their formation at mantle depths. Project supported by the National Natural Science Foundation of China and the Chinese Academy of Sciences.     

Patterns of oxygen isotope depletion,multiple hydrothermal circulation systems,and the cooling history of the Stony Mountain intrusive complex,Colorado

Oxygen isotopic compositions of 27 whole rock and mineral samples from the three intrusive phases of the Stony Mountain stock, San Juan Mountains, Colorado, have been measured and are combined with published analyses to obtain a history of the meteoric water circulation that cooled the intrusions. The order of intrusion was: the Outer Diorite, the Gabbro and the Inner Diorite. The new whole rock data give δ¹⁸O (SMOW) + 1.9 to + 3.7‰ for the Gabbro, and + 0.4 to + 4.9‰ for the Inner Diorite. Five mineral analyses are reported for the Inner Diorite: three feldspars (ranging from + 0.2 to + 4.3), one quartz (+8.2), and one pyroxene (+5.3).All three intrusions are significantly depleted in¹⁸O relative to normal igneous rocks. This depletion occurred by subsolidus exchange of oxygen isotopes, as shown by the correlation between the extent of depletion and the grain size, and by the non-equilibrium¹⁸O concentrations in coexisting minerals. The patterns of¹⁸O depletion, which are complex, suggest that separate hydrothermal circulation systems were set up by the cooling of each intrusion in turn.The minimum water to rock ratio required to effect the observed depletion in the Inner Diorite is approximately 0.18, although the ratio for the total flux was probably much greater. The mineral data show marked¹⁸O depletion in the feldspars and little, if any, depletion in the quartz. Application of oxygen diffusion data for feldspar and quartz leads to the conclusion that the effective temperature for oxygen isotope exchange was below 600°C and above 400°C. Furthermore, these data place constraints on convective cooling times for this intrusion. Minimum times for cooling of the 500-m-diameter Inner Diorite through this temperature range are on the order of 14 to 900 years. For comparison, a maximum time limit of 4000 years would be needed if cooling occurred only by conduction.     

Geochemistry of geopressured hydrothermal waters in the Niigata Sedimentary Basin, Japan

Abstract   Geothermal waters in the Niigata Sedimentary Basin, central Japan, are divided into four groups based on their chemical composition (i.e. Na-SO₄-type, Na-SO₄-Cl-type, Na-Cl-type and Na-Cl-HCO₃-type). The Na-SO₄-type geothermal water forms as a consequence of water–rock interaction and generally occurs in the outer part of the basin. The Na-Cl-type geothermal water is further subdivided into the original Na-Cl-type geopressured thermal water and the mixed Na-Cl-type geothermal water, in terms of its geochemical and isotopic composition. The original Na-Cl-type geopressured thermal water originates from a geopressured hydrothermal system containing the altered fossil formation waters that are sealed at depth. It moves up to the upper part of the depositional succession or the ground, and generally does not mix with groundwater that is of meteoric origin. This type of water is cooled by heat conduction. The concentration of Cl^– in this type of thermal water is very similar to that in seawater. The δD and δ¹⁸O values are approximately constant and independent of temperature. The original Na-Cl-type geopressured thermal water is distributed mainly along anticlinal axes in folded Neogene formations. The mixed Na-Cl-type geothermal water is related to the expulsion activity of the geopressured hydrothermal system and occurs mostly along active faults. It is formed by shallow groundwater of meteoric origin being mixed with geopressured hydrothermal water when the geopressured hydrothermal system was expulsed along active faults by paroxysmal tectonic events.     

Stable isotope ratios of carbon,nitrogen and oxygen in killer whales (Orcinus orca) stranded on the coast of Hokkaido,Japan

We analyzed δ¹³C, δ¹⁵N and δ¹⁸O in the muscle and liver from killer whales stranded on the coast of Japan. The δ¹⁵N values in the muscle samples from calves were apparently higher than those in their lactating mothers, suggesting that nursing may result in the higher δ¹⁵N values in the muscle samples of calves. The δ¹⁵N value in the muscle samples of male and female whales, except for the calves, were positively correlated with the δ¹³C values and body length, suggesting that the increases in δ¹⁵N were due to the growth of the whales and increase in their trophic level. In contrast, the δ¹⁸O values in the muscle samples of female whales except for the calves were negatively correlated with the δ¹³C and δ¹⁵N values. The δ¹⁸O may be lower in whales occupying higher trophic positions (δ¹⁵N), although it might also be affected by geographic and climatic conditions.     

Factors controlling stable oxygen,hydrogen and carbon isotope ratios in regional groundwater of the eastern United Arab Emirates (UAE)

Increasing groundwater salinity and depletion of the aquifers are major concerns in the UAE. Isotopes of oxygen, hydrogen, and carbon concentrations in groundwater were used to estimate evaporation loss using the isotopes of oxygen and hydrogen, and using a carbon isotope to trace inorganic carbon cycling in two main aquifers in the eastern part of the United Arab Emirates. The δD‐δ¹⁸O of groundwater samples plotted on a line given by: δD = 4 δ¹⁸O + 4 ·4 (r² = 0·4). In comparison, the local meteoric water line (LMWL) has been defined by the line: δD = 8 δ¹⁸O + 15. In order to better understand the system investigated, samples were separated into two groups based on the δD‐δ¹⁸O relationship. These are (1) samples that plot above the LMWL (δD = 6·1 δ¹⁸O + 12·4, r² = 0·8) and which are located predominantly in the north of the study area, and (2) samples that plot below the LMWL (δD = 5·6 δ¹⁸O + 6·2, r² = 0·8) and which are mostly distributed in the south. Slopes for both the groups are similar and lower than that for LMWL indicating potential evaporation of recharging water. However, the y‐intercept, which differs between the two groups, suggests evaporation of return flow and evapotranspiration in the unsaturated zone to be more significant in the south. This is attributed to intense agricultural activities in the region. Samples from the eastern Gravel Plain aquifer have δ¹³C and dissolved inorganic carbon (DIC) values in the range from ? 10 to 17‰, and 12–100 mg C/l, respectively, while the range for those from the Ophiolite aquifer is from ? 11 to ? 16.4‰, and 16–114 mg C/l respectively. This suggests the control of C‐3 and C‐4 plants on DIC formation, an observation supported by the range δ¹³C of soil organic matter (from ? 18·5 to ? 22·1‰.) Copyright © 2007 John Wiley & Sons, Ltd.     

Carbon isotope ratios of C4 plants in loess areas of North China

Carbon isotope ratios (δ ¹³C) of 89 C₄ plant samples were determined from the loess area in North China. δ ¹³C values vary between −10.5‰ and −14.6‰ with a mean of −12.6‰. Along a precipitation gradient from the semi-moist area to the semiarid area, then to the arid area, the δ ¹³C values of C₄ plants show a slight decreasing trend. The δ ¹³C values of C₄ plants in the dry season are found lower than those in the wet season. These trends are opposite to those observed for C₃ species.     

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.     

Influence of the Danube River inputs on C and N stable isotope ratios of the Romanian coastal waters and sediment (Black Sea)

The main aim of this study was to estimate the influence of the seasonal variations of the Danube River particulate organic matter (POM) inputs on the Black Sea surface seawater POM and upper layer of sediments along the Romanian coast. Ratios of carbon ((13)C/(12)C) and nitrogen ((15)N/(14)N) stable isotopes allowed differentiating river and marine organic matter sources. Danube River POM presented significantly lower average values of delta(13)C (-27.52+/-0.88 per thousand) and delta(15)N (4.88+/-1.45 per thousand) than seawater POM (delta(13)C=-24.70+/-2.37 per thousand and delta(15)N=6.75+/-1.96 per thousand), whereas surface sediment presented average values similar to seawater POM (delta(13)C=-24.02+/-2.39 per thousand and delta(15)N=7.29+/-2.16 per thousand). Stable isotope values showed that the Danube River influence on marine ecosystems decreased from the North to the South of the Romanian coast. Strong seasonal variations of C and N isotopic signatures were observed in all compartments studied with generally higher values in spring when the river was flooding.     

Geographical distribution of helium isotope ratios in northeastern Japan

In order to study the precise geographical distribution of helium isotope ratios in northeastern Japan and compare it with geophysical data, we collected 43 gas and water samples from hot and mineral springs in the region where the ratio had never been reported, and measured the ³He/⁴He and ⁴He/²⁰Ne ratios of these samples. It was found that the ³He/⁴He ratios show clear contrasts between the forearc and the back-arc regions in the Tohoku district in northeastern Japan. In the forearc region, the ratios are smaller than 1 R_A (1 R_A = 1.4 × 10⁻⁶; R_A means the ³He/⁴He ratio of the atmosphere). On the other hand, those along the volcanic front and in the back-arc region are apparently higher. Moreover, we found a variation in the ³He/⁴He ratios along the volcanic front. In Miyagi Prefecture (38–39°N), the ratios range from 2 to 5 R_A. On the other hand, the ratios are less than 1 R_A in and around the southern border between Iwate and Akita Prefectures (39–39.5°N). Comparing the distribution of helium isotope ratios to results of recent geophysical studies, we found that the features in geographical distribution of helium isotope ratios are similar to those of seismic low-velocity zone distributions and high Qp⁻¹ distributions in the uppermost mantle. These observations strongly suggest that the helium isotope ratios reflect the distribution of melts in the uppermost mantle and are a useful tool for investigating the origin, behavior, and distribution of deep fluids and melts.     

The density of North Atlantic and North Pacific deep waters

The densities of seventeen samples of seawater from GEOSECS stations 27 (North Atlantic) and 217 (North Pacific) have been measured with a vibrating flow densimeter at 25°C. The densities of the deep samples were found to be 5 ± 1.5and16 ± 3.6ppm greater, for the North Atlantic and North Pacific, respectively, than predicted by the equation of state of Millero, Gonzalez and Ward (1976) derived for seawaters of constant relative composition. The results are in good agreement with the density anomalies predicted by Brewer and Bradshaw (1975) on the basis of the observed increase of dissolved silica, alkalinity and total carbon dioxide in oceanic deep waters. The application of these corrections results in an agreement with the Millero, Gonzalez and Ward (1976) equation of state to ±4 ppm.     

Oxygen isotope evidence for submarine hydrothermal alteration of the Del Puerto ophiolite, California

The oxygen isotope compositions and metamorphic mineral assemblages of hydrothermally altered rocks from the Del Puerto ophiolite and overlying volcaniclastic sedimentary rocks at the base of the Great Valley sequence indicate that their alteration occurred in a submarine hydrothermal system. Whole rock δ¹⁸O compositions decrease progressively down section (with increasing metamorphic grade): +22.4‰ (SMOW) to +13.8 for zeolite-bearing volcaniclastic sedimentary rocks overlying the ophiolite; +19.6 to +11.6 for pumpellyite-bearing metavolcanic rocks in the upper part of the ophiolite's volcanic member; +12.3 to +8.1 for epidote-bearing metavolcanic rocks in the lower part of the volcanic member; +8.5 to +5.7 for greenschist facies rocks from the ophiolite's plutonic member; +7.6 to +5.8 for amphibolite facies or unmetamorphosed rocks from the plutonic member.

Modelling of fluid-rock interaction in the Del Puerto ophiolite indicates that the observed pattern of upward enrichment in whole rock δ¹⁸O can be best explained by isotopic exchange with discharging¹⁸O-shifted seawater at fluid/rock mass ratios near 2 and temperatures below 500°C.¹⁸O-depleted plutonic rocks necessarily produced during hydrothermal circulation were later removed as a result of tectonism. Submarine weathering and later burial metamorphism at the base of the Great Valley sequence cannot by itself have produced the zonation of hydrothermal minerals and the corresponding variations in oxygen isotope compositions. The pervasive zeolite and prehnite-pumpellyite facies mineral assemblages found in the Del Puerto ophiolite may reflect its origin near an island arc rather than deep ocean spreading center.     

Strontium isotope ratios in volcanic rocks from the South Sandwich Islands

⁸⁷Sr/⁸⁶Sr ratios in the island-arc tholeiite series from the South Sandwich Islands cluster about a value of 0.7040. There is no apparent correlation of strontium isotope values with any major chemical component or with Rb/Sr ratios. The uniformity of the⁸⁷Sr/⁸⁶Sr values is consistent with the fractional crystallization relationship previously proposed for this suite. Though higher than values reported for ocean-floor tholeiites they are not significantly different from ratios reported for calc-alkaline island-arcs.