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1.
In contrast to most other arcs with oceanic plate subduction, the Aegean arc is characterized by continent–continent subduction. Noble gas abundances and isotopic compositions of 45 gas samples have been determined from 6 volcanoes along the arc, 2 islands in the back-arc region and 7 sites in the surrounding areas. The 3He/4He ratios of the samples ranged from 0.027RA to 6.2RA (RA denotes the atmospheric 3He/4He ratio of 1.4×10−6), demonstrating that even the maximum 3He/4He ratio in the region is significantly lower than the maximum ratios of most oceanic subduction systems, which are equal to the MORB value of 8±1 RA. Regional variations in the 3He/4He ratio were observed both along and across the arc. The maximum 3He/4He ratio was obtained from Nisyros volcano located in the eastern end of the arc, and the ratio decreased westward possibly reflecting the difference in potential degree of crustal assimilation or the present magmatic activity in each volcano. Across the volcanic arc, the 3He/4He ratio decreased with an increasing distance from the arc front, reaching a low ratio of 0.063RA in Macedonia, which suggested a major contribution of radiogenic helium derived from the continental crust. At Nisyros, a temporal increase in 3He/4He ratio due to ascending subsurface magma was observed after the seismic crisis of 1995–1998 and mantle neon was possibly detected. The maximum 3He/4He ratio (6.2RA) in the Aegean region, which is significantly lower than the MORB value, is not probably due to crustal assimilation at shallow depth or addition of slab-derived helium to MORB-like mantle wedge, but inherent characteristics of the subcontinental lithospheric mantle (SCLM) beneath the Aegean arc.  相似文献   

2.
We have collected 34 hot spring and mineral spring gases and waters in the Chugoku and Kansai districts, Southwestern Japan and measured the 3He/4He and 4He/20Ne ratios by using a noble gas mass spectrometer. Observed 3He/4He and 4He/20Ne ratios range from 0.054 Ratm to 5.04 Ratm (where Ratm is the atmospheric 3He/4He ratio of 1.39 × 10−6) and from 0.25 to 36.8, respectively. They are well explained by a mixing of three components, mantle-derived, radiogenic, and atmospheric helium dissolved in water. The 3He/4He ratios corrected for air contamination are low in the frontal arc and high in the volcanic arc regions, which are consistent with data of subduction zones in the literature. The geographical contrast may provide a constraint on the position of the volcanic front in the Chugoku district where it was not well defined by previous works. Taking into account the magma aging effect, we cannot explain the high 3He/4He ratios of the volcanic arc region by the slab melting of the subducting Philippine Sea plate. The other source with pristine mantle material may be required. More precisely, the highest and average 3He/4He ratios of 5.88 Ratm and 3.8±1.6 Ratm, respectively, in the narrow regions near the volcanic front of the Chugoku district are lower than those in Kyushu and Kinki Spot in Southwestern Japan, but close to those in NE Japan. This suggests that the magma source of the former may be related to the subduction of the Pacific plate, in addition to a slight component of melting of the Philippine Sea slab.  相似文献   

3.
Secular variations in 13C/12C ratios and chemical compositions of gas samples from October 1986 to July 1992 are reported from a 92–95 °C steam well located about 3 km north of Mt. Mihara, an active volcano on Izu-Oshima Island, Japan. The δ13C value steeply increased from −2.97‰ (relative to PDB carbonate) in December 1986 to −1.15‰ in March 1988 and then gradually decreased to −1.75‰ in July 1992. Over the same period, the CO2 content changed similarly with time, even though the experimental error is relatively large. These variations are consistent with helium isotope changes. Initially rapid and then slow enhancements of 3He/4He ratio, δ13C value and CO2 content are invoked by violent eruptions of Izu-Oshima volcano from 15 November to 18 December 1986. After the eruptive activity, depletion of magmatic gas emission and subsequent mixing with crustal fluids in the hydrothermal system may produce the gradual decreases of 3He/4He ratio, δ13C value and CO2 content. Taking into account the rates of these decreases, we suggest that helium and carbon isotope ratios will return to the situation of before the magmatic eruption within 15 years.  相似文献   

4.
3He/4He ratios in lavas erupted during the last 360 years at Mt. Vesuvius are between 2.2 and 2.7 RA (RA = atmospheric ratio of 1.39 × 10−6), and are among the lowest values measured in young volcanic rocks. They are also identical to values measured in summit crater fumaroles sampled during 1987–1991. This agreement indicates that the 3He/4He ratio in the crater fumaroles faithfully tracks the magmatic value. The relatively low and uniform 3He/4He ratio in the lavas reflects either a mantle source enriched in (U + Th)/3He, or a mixture of magmatic and crustal components.  相似文献   

5.
This study presents baseline data for future geochemical monitoring of the active Tacaná volcano–hydrothermal system (Mexico–Guatemala). Seven groups of thermal springs, related to a NW/SE-oriented fault scarp cutting the summit area (4,100m a.s.l.), discharge at the northwest foot of the volcano (1,500–2,000m a.s.l.); another one on the southern ends of Tacaná (La Calera). The near-neutral (pH from 5.8 to 6.9) thermal (T from 25.7°C to 63.0°C) HCO3–SO4 waters are thought to have formed by the absorption of a H2S/SO2–CO2-enriched steam into a Cl-rich geothermal aquifer, afterwards mixed by Na/HCO3-enriched meteoric waters originating from the higher elevations of the volcano as stated by the isotopic composition (δD and δ18O) of meteoric and spring waters. Boiling temperature fumaroles (89°C at ~3,600m a.s.l. NW of the summit), formed after the May 1986 phreatic explosion, emit isotopically light vapour (δD and δ18O as low as −128 and −19.9‰, respectively) resulting from steam separation from the summit aquifer. Fumarolic as well as bubbling gases at five springs are CO2-dominated. The δ13CCO2 for all gases show typical magmatic values of −3.6 ± 1.3‰ vs V-PDB. The large range in 3He/4He ratios for bubbling, dissolved and fumarolic gases [from 1.3 to 6.9 atmospheric 3He/4He ratio (R A)] is ascribed to a different degree of near-surface boiling processes inside a heterogeneous aquifer at the contact between the volcanic edifice and the crystalline basement (4He source). Tacaná volcano offers a unique opportunity to give insight into shallow hydrothermal and deep magmatic processes affecting the CO2/3He ratio of gases: bubbling springs with lower gas/water ratios show higher 3He/4He ratios and consequently lower CO2/3He ratios (e.g. Zarco spring). Typical Central American CO2/3He and 3He/4He ratios are found for the fumarolic Agua Caliente and Zarco gases (3.1 ± 1.6 × 1010 and 6.0 ± 0.9 R A, respectively). The L/S (5.9 ± 0.5) and (L + S)/M ratios (9.2 ± 0.7) for the same gases are almost identical to the ones calculated for gases in El Salvador, suggesting an enhanced slab contribution as far as the northern extreme of the Central American Volcanic Arc, Tacaná.  相似文献   

6.
Helium isotopic ratios ranging from 20 to 32 times the atmospheric 3He/4He(RA) have been observed in a suite of 15 basaltic glasses from the Loihi Seamount. These ratios, which are up to four times higher than those of MORB glasses and more than twice those of nearby Kilauea, are strongly suggestive of a primitive source of volatiles supplying this volcanism. The Loihi glasses measured span a broad compositional range, and the 3He/4He ratios were found to be generally lower for the alkali basalts than for the tholeiites. The component with a lower 3He/4He ratio appears to be associated with olivine xenocrysts, within which fluid inclusions are probably the carrier of contaminant helium. One Loihi sample has a much lower isotopic ratio (<5 RA), but a combination of low He concentration, high vesicularity, and presence of cracks lined with clay minerals suggests that the low ratio is due to gas loss and contamination by atmospheric helium.Crushing and melting experiments show that for modest vesicularities (<5% by volume) the Loihi glasses obey a MORB-type partitioning trend, but at higher vesicularities the data show considerably more scatter due to volatile mobilization. The high vesicularities, low extrusion pressure and generally low helium concentrations are consistent with a considerable degree of degassing. Analyses of dunites, plus a correlation between total helium concentrations with xenocryst abundances also suggest that xenocrysts are a significant carrier of contaminating (low 3He/4He) helium.3He/4He ratios from samples of other Hawaiian volcanoes (Kilauea, Mauna Loa, Hualalai, and Mauna Kea) show a smooth decrease in 3He/4He with increasing volcano age and volume. We interpret this to be a synoptic picture of the time evolution of a hot-spot diapir: the earliest stage is characterized by primitive (> 30 RA) helium with some (variable) component of lithospheric contamination added during “breakthrough”, while the later stages are characterized by a relaxation toward lithospheric 3He/4He ratios (～ 8 RA) due to isolation of the diapir from the mantle below (as the plate moves on), and subsequent mining of the inherited helium and contamination from the surrounding lithosphere. The abrupt contrast in 3He/4He ratios between Kilauea and Loihi, despite their close proximity, is indicative of the small lateral extent of the plume.  相似文献   

7.
Noncondensible gases from hot springs, fumaroles, and deep wells within the Valles caldera geothermal system (210–300°C) consist of roughly 98.5 mol% CO2, 0.5 mol% H2S, and 1 mol% other components. 3He/4He ratios indicate a deep magmatic source (R/Ra up to 6) whereas δ13C–CO2 values (−3 to −5‰) do not discriminate between a mantle/magmatic source and a source from subjacent, hydrothermally altered Paleozoic carbonate rocks. Regional gases from sites within a 50-km radius beyond Valles caldera are relatively enriched in CO2 and He, but depleted in H2S compared to Valles gases. Regional gases have R/Ra values ≤1.2 due to more interaction with the crust and/or less contribution from the mantle. Carbon sources for regional CO2 are varied. During 1982–1998, repeat analyses of gases from intracaldera sites at Sulphur Springs showed relatively constant CH4, H2, and H2S contents. The only exception was gas from Footbath Spring (1987–1993), which experienced increases in these three components during drilling and testing of scientific wells VC-2a and VC-2b. Present-day Valles gases contain substantially less N2 than fluid inclusion gases trapped in deep, early-stage, post-caldera vein minerals. This suggests that the long-lived Valles hydrothermal system (ca. 1 Myr) has depleted subsurface Paleozoic sedimentary rocks of nitrogen. When compared with gases from many other geothermal systems, Valles caldera gases are relatively enriched in He but depleted in CH4, N2 and Ar. In this respect, Valles gases resemble end-member hydrothermal and magmatic gases discharged at hot spots (Galapagos, Kilauea, and Yellowstone).  相似文献   

8.
Geothermal gases from submarine and subaerial hot springs in Ensenada, Baja California Norte, Mexico, were sampled for determination of gas chemistry and helium, nitrogen and stable carbon isotope composition. The submarine hot spring gas is primarily nitrogen (56.1% by volume) and methane (43.5% by volume), whereas nearby subaerial hot spring gases are predominantly nitrogen (95–99% by volume). The N2/Ar ratios and σ 15N values of the subaerial hot spring gas indicate that it is atmospheric air, depleted in oxygen and enriched in helium. The submarine hot spring gas is most probably derived from marine sediments of Cretaceous age rich in organic matter. CH4 is a major component of the gas mixture (σ 13C = −44.05%0), with only minor amounts of CO2 (σ13C= −10.46%0). The σ15N of N2 is + 0.2%0 with a very high N2/Ar ratio of 160. The calculated isotopic equilibra tion temperature for CH4---CO2 carbon exchange at depth in the Punta Banda submarine geothermal field is approximately 200°C in agreement with other geothermometry estimates. The 3He/4He ratios of the hot spring gases range from 0.3 to 0.6 times the atmospheric ratio, indicating that helium is predominantly derived from the radioactive decay of U and Th within the continental crust. Thus, not all submarine hydrothermal systems are effective vehicles for mantle degassing of primordial helium.  相似文献   

9.
Gas concentrations and isotopic compositions of water have been measured in hydrothermal waters from 13°N on the East Pacific Rise. In the most Mg-depleted samples ( 5 × 10−3 moles/kg) the gas concentrations are: 3–4.5 × 10−5 cm3 STP/kg helium, 0.62–1.24 cm3 STP/kg CH4, 10.80–16.71 × 10−3 moles/kg CO2. The samples contain large quantities (95–126 cm3/kg) of H2 and some carbon monoxide (0.26–0.36 cm3/kg) which result from reaction with the titanium sampling bottles. δ13C in methane and CO2 (−16.6 to −19.5 and −4.1 to −5.5 respectively) indicate temperatures between 475 and 550°C, whereas δ13CCO is compatible with formation by reduction of CO2 on Ti at 350°C close to the sampling temperature.3He/4He are very homogeneous at (7.5 ± 0.1)RA(3He/4He = 1.0 × 10−5) and very similar to already published data as well as CH4/3He ratios between 1.4 and 2.1 × 106.18O and D in water show enrichments from 0.39 to 0.69‰ and from 0.62 to 1.49‰ respectively. These values correspond to W/R ratios of 0.4–7. The distinct18O enrichments indicate that the isotopic composition of the oceans is not completely buffered by the hydrothermal circulations. The3He-enthalpy relationship is discussed in terms of both hydrothermal heat flux and3He mantle flux.  相似文献   

10.
A large data base has recently accumulated on the concentrations of helium isotopes in diamonds mined from various regions. It was noted earlier (Ozima et al. (1985) [1]; Lal et al. (1989) [2]) that the frequency distribution of the4He concentrations is a fairly narrow one, whereas that of3He concentrations is a broad one with no pronounced peaks. The ratios 3He/4He, on the other hand show a broad maximum around 2 Ra (Ra equals atmospheric 3He/4He ratio, = 1.40 × 10−6) with a slow decrease over two orders of magnitude on either side. Does this imply that the diamonds sample a wide variety of helium reservoirs having a range of 3He/4He ratios but somehow attain similar4He concentrations? We propose that in a majority of the diamonds studied,4He is primarily due to implantation of radiogenic alpha particles from the host material after emplacement in the crust, usually kimberlite, and that the concentrations of4He in diamonds often get appreciably altered by this process. Thus the4He trapped in the diamond at the time of its crystallization is usually overwhelmed by the implanted helium and the measured 3He/4He ratios do not generally correspond to any “sources” in the mantle. However, the implanted4He resides in the outer 16 μm of the diamond, and the intrinsic4He and 3He/4He ratios in the diamond can be studied if its outer layers are removed.The wider implications of diamond being the “target” material for nuclear reaction products from the host material are discussed. Radiogenic3He produced in the host material is also implanted in the diamond, but this contribution is small on a gross basis. However, since the depth of implantation of3He is greater than that of4He, some of the very high 3He/4He ratios observed in diamonds could be due to the “implantation” of radiogenic3He. The radiogenic reactions in the host material can also contribute to appreciable21Ne in diamonds.  相似文献   

11.
Results are presented on scubadiving investigations carried out on thermal manifestations in the area of Panarea (Aeolian Islands). The area investigated falls inside a caldera which extends from the main island to the group of islets located to the northeast. The distribution of the gaseous manifestations is regulated by the NE-SW, NW-SE and N-S regional tectonic directrices, through which the more recent basic magma intruded, giving rise to dikes and pillow lavas. fO2-temperature relation of the gases sampled in the investigated area was calculated to be: logfO2 = 11−24,593/T which indicates that a buffering mechanism acted on the gases as they cooled down during their ascent. The high 3He/4He ratio (6 × 10−6) and the δ13C = −3.2%. (PDB), suggest the presence of a magmatic component in the gas feeding the investigated manifestations. The above relations and the almost constant high He/N2 ratio suggest that all the fumaroles are fed by the same deep hot fluids. On the basis of both the chemical characters of the fluids and the geothermo-barometric data, a deep geothermal body, having a temperature of about 240°C, is recognized. Two other shallower thermal aquifers, with a temperature of 170–210°C, are identified. A circulation pattern of the geothermal fluids is also proposed. On the basis of calculations regarding the convective energy released by the geothermal system of Panarea, and the magmatic mass responsible for the positive gravimetric anomaly of the area, it was estimated that the last volcanic activity took place less then 10,000 years ago.  相似文献   

12.
Oldoinyo Lengai is the world's only active carbonatite volcano and considerable debate still surrounds the genesis of its magmas. Gases were collected from two fumaroles discharging close to the then active vent in October 2003. Measured fumarole temperatures were ≤ 195°C, despite the nearby, vigorous eruptive activity. Gases were sampled and analysed for noble gas isotopes. Freshly erupted natrocarbonatite lavas, a 1917 nephelinite and a sub-recent wollastonite bearing rock were also collected and analysed for noble gas isotopes using vacuum crushing techniques. In all the lava samples the neon, argon, krypton and xenon isotope ratio data are indistinguishable from air implying atmospheric contamination of the hygroscopic rocks. In the fumaroles, measured 3He/4He ratios are between 4 and 7 R/Ra. This range is similar to published values for silicate xenoliths of the East African Rift implying a local lithospheric mantle source for the volatile component of the Lengai magmas. It is still unclear if the natrocarbonatites themselves come from this region, or if fractionation and/or liquid immiscibility generate the carbonate magmas from a silicate melt within the crust itself.  相似文献   

13.
The noble gas nuclide abundances and isotopic ratios of the upmost layer of Fe-Mn crusts from the western and central Pacific Ocean have been determined. The results indicate that the He and Ar nu- clide abundances and isotopic ratios can be classified into two types: low 3He/4He type and high 3He/4He type. The low 3He/4He type is characterized by high 4He abundances of 191×10-9 cm3·STP·g-1 on average, with variable 4He, 20Ne and 40Ar abundances in the range (42.8―421)×10-9 cm3·STP·g-1, (5.40―141)×10-9 cm3·STP·g-1, and (773―10976)×10-9 cm3·STP·g-1, respectively. The high 3He/4He samples are characterized by low 4He abundances of 11.7×10-9 cm3·STP·g-1 on average, with 4He, 20Ne and 40Ar abundances in the range of (7.57―17.4)×10-9 cm3·STP·g-1, (10.4―25.5)×10-9 cm3·STP·g-1 and (5354―9050)×10-9 cm3·STP·g-1, respectively. The low 3He/4He samples have 3He/4He ratios (with R/RA ratios of 2.04―2.92) which are lower than those of MORB (R/RA=8±1) and 40Ar/36Ar ratios (447―543) which are higher than those of air (295.5). The high 3He/4He samples have 3He/4He ratios (with R/RA ratios of 10.4―12.0) slightly higher than those of MORB (R/RA=8±1) and 40Ar/36Ar ratios (293―299) very similar to those of air (295.5). The Ne isotopic ratios (20Ne/22Ne and 21Ne/22Ne ratios of 10.3―10.9 and 0.02774―0.03039, respectively) and the 38Ar/36Ar ratios (0.1886―0.1963) have narrow ranges which are very similar to those of air (the 20Ne/22Ne, 21Ne/22Ne, 38Ar/36Ar ratios of 9.80, 0.029 and 0.187, respectively), and cannot be differentiated into different groups. The noble gas nuclide abundances and isotopic ratios, together with their regional variability, suggest that the noble gases in the Fe-Mn crusts originate primarily from the lower mantle. The low 3He/4He type and high 3He/4He type samples have noble gas characteristics similar to those of HIMU (High U/Pb Mantle)- and EM (Enriched Mantle)-type mantle material, respectively. The low 3He/4He type samples with HIMU-type noble gas isotopic ratios occur in the Magellan Seamounts, Marcus-Wake Seamounts, Marshall Island Chain and the Mid-Pacific Sea- mounts whereas the high 3He/4He type samples with EM-type noble gas isotopic ratios occur in the Line Island Chain. This difference in noble gas characteristics of these crust types implies that the MagellanSeamounts, Marcus-Wake Seamounts, Marshall Is- land Chain, and the Mid-Pacific Seamounts originated from HIMU-type lower mantle material whereas the Line Island Chain originated from EM-type lower mantle material. This finding is consistent with varia- tions in the Pb-isotope and trace element signatures in the seamount lavas. Differences in the mantlesource may therefore be responsible for variations in the noble gas abundances and isotopic ratios in the Fe-Mn crusts. Mantle degassing appears to be the principal factor controlling noble gas isotopic abundances in Fe-Mn crusts. Decay of radioactive isotopes has a negligible influence on the nuclide abundances and isotopic ratios of noble gases in these crusts on the timescale of their formation.  相似文献   

14.
A genetic algorithm inversion of receiver functions derived from a dense seismic network around Iwate volcano, northeastern Japan, provides the fine S wave velocity structure of the crust and uppermost mantle. Since receiver functions are insensitive to an absolute velocity, travel times of P and S waves propagating vertically from earthquakes in the subducting slab beneath the volcano are involved in the inversion. The distribution of velocity perturbations in relation to the hypocenters of the low-frequency (LF) earthquakes helps our understanding of deep magmatism beneath Iwate volcano. A high-velocity region (dVS/VS=10%) exists around the volcano at depths of 2–15 km, with the bottom depth decreasing to 11 km beneath the volcano’s summit. Just beneath the thinning high-velocity region, a low-velocity region (dVS/VS=−10%) exists at depths of 11–20 km. Intermediate-depth LF (ILF) events are distributed vertically in the high-velocity region down to the top of the low-velocity region. This distribution suggests that a magma reservoir situated in the low-velocity region supplies magma to a narrow conduit that is detectable by the hypocenters of LF earthquakes. Another broad low-velocity region (dVS/VS=−5 to −10%) occurs at depths of 17–35 km. Additional clusters of deep LF (DLF) events exist at depths of 32–37 km in the broad low-velocity zone. The DLF and ILF events are the manifestations of magma movement near the Moho discontinuity and in the conduit just beneath the volcano, respectively.  相似文献   

15.
Mantle-derived volatiles in continental crust: the Massif Central of France   总被引：1，自引：0，他引：1  
CO2-rich gases and groundwaters from springs and boreholes originating within the basement of the Massif Central have variable3He/4He ratios with correspondingR/Ra values ranging from 0.8 to 5.5 and 0.3 to 2.8 respectively, indicating the presence of a significant component of mantle helium. Molar concentrations of rare gases in the CO2-rich gases are approximately 5 orders of magnitude greater than in the waters and suggest that a near-surface Henry's Law fractionation has occurred between exsolving CO2 and water.δ13C values of the CO2-rich gases are in the range −4.2 to −6.1‰, i.e. in that range normally attributed to mantle carbon, but which could also represent an average crustal composition and therefore do not discriminate between mantle and crustal sources.C/3He ratios show 4 orders of magnitude variation from 1.4 × 1012 to 5 × 108 and, compared to a mantleC/3He ratio of 109, indicate that either a complex fractionation has occurred between mantle helium and mantle CO2 or more likely that mantle rare gases have been diluted by large quantities of CO2 with an average crustal carbon isotope composition. The regional distribution of3He and C does not show any obvious relationship to age or proximity of volcanic centres or major faults, suggesting that mantle-derived C and He components decoupled from their silicate melt sources at some depth.The results from this area of active fluid circulation suggest that C-isotope data derived from metamorphic terrains should be interpreted with great caution, but that input of some mantle-derived carbon is expected to accompany crustal extension.  相似文献   

16.
Sulfur isotope effects during the SO2 disproportionation reaction to form elemental sulfur (3SO2+3H2O→2HSO4−+S+2H+) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO4− and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln αHSO4−–S=6.21×106/T2+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ34S values of HSO4− and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). ΔHSO4−–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO2 disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high ΔHSO4−–S values, whereas contribution of HSO4− produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower ΔHSO4−–S values. Currently, Noboribetsu crater lake contains no HSO4− of magmatic origin. A 40-year period observation of δ34SHSO4− and δ34SS values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO2 to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ34SHSO4− values. The δ18O values of HSO4− and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.  相似文献   

17.
Noble gas isotopes including 3He/4He, 40Ar/36Ar and Xe isotope ratios were determined for coexisting glass and olivine crystals in tholeiitic and alkalic basalts and dunite xenoliths from Loihi Seamount.Glass and coexisting olivine crystals have similar 3He/4He ratios (2.8–3.4) × 10?5, 20 to 24 times the atmospheric ratio (RA), but different 40Ar/36Ar ratios (400–1000). Based on the results of noble gas isotope ratios and microscopic observation, some olivine crystals are xenocrysts. We conclude that He is equilibrated between glass and olivine xenocrysts, but Ar is not.The apparent high 3He/4He ratio (3 × 10?5; = 21 RA) coupled with a relatively high 40Ar/36Ar ratio (4200) for dunite xenoliths (KK 17-5) may be explained by equilibration of He between MORB-type cumulates and the host magma.Except for the dunite xenoliths, noble gas data for these Loihi samples are compatible with a model in which samples from hot spot areas may be explained by mixing between P (plume)-type and M (MORB)-type components with the addition of A (atmosphere)-type component.Excess 129Xe has not been observed due to apparent large mass fractionation among Xe isotopes.  相似文献   

18.
The ophiolites from the Yarlung Zangbo River (Tibet),Southwestern China,were analysed for the con-tents of helium and neon and their isotopic compositions by stepwise heating. The serpentinites from Bainang showed a high 3He/4He value of 32.66Ra (Ra is referred to the 3He/4He ratio in the present air) in 700 ℃ fraction. At lower temperature,all of the dolerites displayed as very high 3He/4He ratios as ones investigated for hotspots. It was clear that the high 3He/4He ratio was one of immanent characterics in the magma source formed the dolerites,suggesting that there was a large amount of deep mantle fluids in these rocks. In the three-isotope diagram of neon,the data points from the ophiolites of the Yarlung Zangbo River were arranged along the Loihi Line. This is in agreement with the characteristics of he-lium isotopes,revealing that the high-3He plume from deep mantle had played an important role in the formation of the Neo-Tethyan Ocean. The helium isotopic compositions in the basalts were far higher than atomospheric value but lower than the average value of MORB,although there were various de-grees of alteration. The possible reasons were that basaltic magmas  相似文献   

19.
The groundwaters of the Great Artesian Basin (Australia) have been previously shown to be accumulating in-situ production helium for groundwaters ages < 50 kyr and an external helium flux equivalent to whole crustal production for groundwater ages > 100 kyr [1,2]. New helium isotope measurements show that the observed in-situ production helium (3He/4He 1.6 × 10−8) is isotopically distinct from the crustal degassing helium flux (3He/4He 6.6 × 10−8). Furthermore, the crustal degassing helium isotope ratio is marginally in excess of the whole crustal production ratio (3He/4He= 3.5 × 10−8) and the production ratio in a variety of continental rock types. This suggests that the upper limit on volatile transport across the mantle-crust boundary beneath the (relatively) stable and “complacent” Australian continent can be characterized by a “conductive-diffusive” helium/heat flux ratio of 2.6 × 1064He atoms mW−1 s−1 which is two orders of magnitude less than the “intrusive-volcanic” ratio of 2.9 × 1084He atoms mW−1 s−1 measured at the Galapagos [16]. These results constrain the transcrustal mantle degassing fluxes of4He and40Ar to be much less than the mid-ocean ridge degassing fluxes; which are much less than the degassing of4He and40Ar from continental crust. Thus, the degassing of the Earth's interior is dominated by magmatic processes but the dominant fluxes of4He and40Ar to the atmosphere must come from the continental crust.  相似文献   

20.
 The 1982 eruption of El Chichón volcano ejected more than 1 km3 of anhydrite-bearing trachyandesite pyroclastic material to form a new 1-km-wide and 300-m-deep crater and uncovered the upper 500 m of an active volcano-hydrothermal system. Instead of the weak boiling-point temperature fumaroles of the former lava dome, a vigorously boiling crater spring now discharges  / 20 kg/s of Cl-rich (∼15 000 mg/kg) and sulphur-poor ( / 200 mg/kg of SO4), almost neutral (pH up to 6.7) water with an isotopic composition close to that of subduction-type magmatic water (δD=–15‰, δ18O=+6.5‰). This spring, as well as numerous Cl-free boiling springs discharging a mixture of meteoric water with fumarolic condensates, feed the crater lake, which, compared with values in 1983, is now much more diluted (∼3000 mg/kg of Cl vs 24 030 mg/kg), less acidic (pH=2.6 vs 0.56) and contains much lower amounts of S ( / 200 mg/kg of SO4, vs 3550 mg/kg) with δ34S=0.5–4.2‰ (+17‰ in 1983). Agua Caliente thermal waters, on the southeast slope of the volcano, have an outflow rate of approximately 100 kg/s of 71  °C Na–Ca–Cl water and are five times more concentrated than before the eruption (B. R. Molina, unpublished data). Relative N2, Ar and He gas concentrations suggest extensional tectonics for the El Chichón volcanic centre. The 3He/4He and 4He/20Ne ratios in gases from the crater fumaroles (7.3Ra, 2560) and Agua Caliente hot springs (5.3Ra, 44) indicate a strong magmatic contribution. However, relative concentrations of reactive species are typical of equilibrium in a two-phase boiling aquifer. Sulphur and C isotopic data indicate highly reducing conditions within the system, probably associated with the presence of buried vegetation resulting from the 1982 eruption. All Cl-rich waters at El Chichón have a common source. This water has the appearence of a "partially matured" magmatic fluid: condensed magmatic vapour neutralized by interaction with fresh volcaniclastic deposits and depleted in S due to anhydrite precipitation. Shallow ground waters emerging around the volcano from the thick cover of fresh pumice deposits (Red waters) are Ca–SO4–rich and have a negative oxygen isotopic shift, probably due to ongoing formation of clay at low temperatures. Received: 21 July 1997 / Accepted: 4 December 1997  相似文献   

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