The 3He distribution in deep water over the Mid-Atlantic Ridge

³He/⁴He ratios in dissolved helium at GEOSECS stations 115, 117, 30, and 120 provide an east-west section across the Mid-Atlantic Ridge at 30°N. Below 1500 m depth, the³He/⁴He profiles show little structure and have values within a few percent of the atmospheric ratio, indicating that the Mid-Atlantic Ridge is not a significant source of injected³He at this latitude. Mean³He/⁴He ratios calculated for the deep water at each station show that the³He/⁴He ratio in the western Atlantic at 30°N is 2–3% higher than in the eastern basin, probably due to mixing between a³He-rich boundary current in the western basin and low-³He deep water to the east.     

Helium isotopes in early Iceland plume picrites: Constraints on the composition of high 3He/4He mantle

A detailed study of the geochemistry of a new suite of early Iceland plume picrites shows that extremely high ³He/⁴He ratios (up to 50 R_a) are found in picrites from Baffin Island and West Greenland. High ³He/⁴He picrites display a wide range in ⁸⁷Sr/⁸⁶Sr (0.70288–0.70403), ¹⁴³Nd/¹⁴⁴Nd (0.51288–0.51308) and incompatible trace element ratios (e.g. La/Sm_n = 0.5–1.6). These overlap the complete range of compositions of mid-ocean ridge basalts and most northern hemisphere ocean island basalts, including Iceland. Crustal contamination modelling in which high-grade Proterozoic crustal basement rocks for the region are mixed with a depleted parent cannot account for the trend displayed by the Baffin Island and West Greenland picrites. This rules out the possibility that the incompatible trace element, Sr and Nd isotope range of the high ³He/⁴He picrites is due to crustal contamination. The compositional range at high ³He/⁴He is also inconsistent with derivation from a primordial-He-rich reservoir that is a residue of ancient mantle depletion. This implies that the composition of the high ³He/⁴He mantle cannot be determined simply by extrapolating ocean island basalt He–Sr–Nd–Pb–Os isotope data.The apparent decoupling of He from trace element and lithophile radiogenic isotope tracers is difficult to attain by simple mixing of a high-[He], high ³He/⁴He reservoir with various depleted and enriched He-poor mantle reservoirs. The possibility that primordial He has diffused into a reservoir with a composition typical of convecting upper mantle cannot be ruled out. If so, the process must have occurred after the development of existing mantle heterogeneity, and requires the existence of a deep, primordial He-rich reservoir.     

Mechanisms of magmatic gas loss along the Southeast Indian Ridge and the Amsterdam -St. Paul Plateau

New analyses of He, Ne, Ar and CO₂ trapped in basaltic glasses from the Southeast Indian Ridge (Amsterdam-St. Paul (ASP) region) show that ridge magmas degas by a Rayleigh distillation process. As a result, the absolute and relative noble gas abundances are highly fractionated with ⁴He/⁴⁰Ar* ratios as high as 620 compared to a production ratio of ∼3 (where ⁴⁰Ar* is ⁴⁰Ar corrected for atmospheric contamination). There is a good correlation between ⁴He/⁴⁰Ar* and the MgO content of the basalt, suggesting that the amount of gas lost from a particular magma is related to the degree of crystallization. Fractional crystallization forces oversaturation of CO₂ because CO₂ is an incompatible element. Therefore, crystallization will increase the fraction of gas lost from the magma. The He-Ar-CO₂-MgO-TiO₂ compositions of the ASP basalts are modeled as a combined fractional crystallization-fractional degassing process using experimentally determined noble gas and CO₂ solubilities and partition coefficients at reasonable magmatic pressures (2-4 kbar). The combined fractional crystallization-degassing model reproduces the basalt compositions well, although it is not possible to rule out depth of eruption as a potential additional control on the extent of degassing. The extent of degassing determines the relative noble gas abundances (⁴He/⁴⁰Ar*) and the ⁴⁰Ar*/CO₂ ratio but it cannot account for large (>factor 50) variations in He/CO₂, due to the similar solubilities of He and CO₂ in basaltic magmas. Instead, variations in CO₂/³He (≡C/³He) trapped in the vesicles must reflect similar variations in the primary magma. The controls on C/³He in mid-ocean ridge basalts (MORBs) are not known. There are no obvious correlated variations between C/³He and tracers of mantle heterogeneity (³He/⁴He, K/Ti etc.), implying that the variations in C/³He are not likely to be a feature of the mantle source to these basalts. Mixing between MORB-like sources and more enriched, high ³He/⁴He sources occurs on and near the ASP plateau, resulting in variable ³He/⁴He and K/Ti compositions (and many other tracers). Using ⁴He/⁴⁰Ar* to track degassing, we demonstrate that mixing systematics involving He isotopes are determined in large part by the extent of degassing. Relatively undegassed lavas (with low ⁴He/⁴⁰Ar*) are characterized by steep ³He/⁴He-K/Ti mixing curves, with high He/Ti ratios in the enriched magma (relative to He/Ti in the MORB magma). Degassed samples (high ⁴He/⁴⁰Ar*) on the other hand have roughly equal He/Ti ratios in both end-members, resulting in linear mixing trajectories involving He isotopes. Some degassing of ASP magmas must occur at depth, prior to magma mixing. As a result of degassing prior to mixing, mixing systematics of oceanic basalts that involve noble gas-lithophile pairs (e.g. ³He/⁴He vs. ⁸⁷Sr/⁸⁶Sr or ⁴⁰Ar/³⁶Ar vs. ²⁰⁶Pb/²⁰⁴Pb) are unlikely to reflect the noble gas composition of the mantle source to the basalts. Instead, the mixing curve will reflect the extent of gas loss from the magmas, which is in turn buffered by the pressure of combined crystallization-degassing and the initial CO₂ content.     

TritiogenicHe in groundwater in Takaoka

³He/⁴He ratios up to 3.5 times the ratio of atmospheric He were found in groundwater samples. The³He enrichment can be attributed to radiogenic³He produced by in-situ beta-decay of³H. This shows that tritiogenic³He is accumulating in confined waters. From tritiogenic³He and³H concentrations, ages of groundwaters can be calculated. Detection of tritiogenic³He gives a tool to trace a tritium contamination which occurred in the past and cannot be assessed only by the³H counting method.     

Rare gas isotopic compositions in natural gases of Japan

Isotopic and elemental compositions of rare gases in various types of gas samples collected in the Japanese Islands were investigated. Excess³He was found in most samples. Many samples showed a regionally uniform high³He/⁴He ratio of about 7 times the atmospheric ratio. The He concentrations varied from 0.6 to 1800 ppm, and they were low in CO₂-rich gases and high in N₂-rich gases. Ne isotopic deviations from the atmospheric Ne were detected in most volcanic gases. The deviations and the elemental abundance patterns in volcanic gases can be explained by a mixing between two components, one is mass fractionated rare gases and the other is isotopically atmospheric and is enriched in heavy rare gas elements. Ar was a mixture of mass fractionated Ar, atmospheric Ar and radiogenic Ar, and the contribution of radiogenic⁴⁰Ar was small in all samples. Except for He, elemental abundance patterns were progressively enriched in the heavier rare gases relative to the atmosphere. Several samples were highly enriched in Kr and Xe relative to the abundance pattern of dissolution equilibrium of atmospheric rare gases in water. The component which is highly enriched in heavy rare gases may be released from sedimentary materials in the crust.     

Helium isotopic variability within single diamonds from the Orapa kimberlite pipe

The distribution and isotopic composition of helium has been measured in a suite of well-characterized one-carat diamonds from the Orapa kimberlite, Botswana. Crushing of the diamonds in vacuo indicates that most of the helium is contained by the matrix (generally greater than 90%), rather than by the inclusions. Step-heating experiments, performed on inclusion-free fragments remaining after crushing, indicate that the³He/⁴He ratio is variablewithin individual diamonds. The fragments, as small as 10 mg, were heated in two timed steps, both at 2000°C. In every case, lower³He/⁴He ratios are observed in the first graphitization step (0.05–3 × atmospheric), while the last heating step releases helium with systematically higher³He/⁴He ratio (30–80 × atmospheric). We suggest that this internal isotopic variability is the result of stepwise graphitization: the first heating step initiates graphitization, which nucleates around defects, and the second heating step graphitizes the relatively defect-free regions of the diamond. The³He/⁴He ratio measured, using the partial graphitization technique, differs by up to a factor of 100 within a single specimen. The inclusion-free fragments release small quantities of helium below 2000°C, which suggests that helium release is obtained only by graphitization. The³He contents of the monocrystalline diamonds are relatively constant (at 3 × 10⁻¹³ cm³ STP/gram) and indicate that most of the isotopic variability is due to radiogenic⁴He. The variations in⁴He content are either related to zoning of Th and U in the diamonds (i.e., in-situ decay), to zoning of inherited⁴He, or to implantation of α-particles from a Th and U rich environment (i.e., kimberlite). Because the Orapa diamonds were mined from roughly 40 m depth in the kimberlite, spallation reactions from cosmic ray interactions are not a significant source of³He. However, calculations based on the age of the kimberlite (90 m.y.) and reasonable Th and U abundances suggest that most of the³He in the Orapa diamonds could be produced by⁶Li(n, α)T in the diamond. Although this may not be true of all diamonds, nuclear reactions in the crust and mantle (including spallation reactions at the surface) can explain many of the high³He/⁴He ratios previously reported for diamonds.     

Water-saturated oceanic lavas from the Manus Basin: volatile behaviour during assimilation–fractional crystallisation–degassing (AFCD)

We have analysed volatiles (H₂O, He, Ar, CO₂) in differentiated (basaltic andesite, dacite) volcanic glasses dredged at a depth of ca. 2000 m in the eastern part of the Manus Basin between 151°20′ and 152°10′ E. These samples have Sr–O–B isotopic ratios that show that they most likely represent lavas evolved from a common magma source. Since these glasses are very fresh, they provide a unique opportunity to study the behaviour of magmatic volatiles during assimilation–fractional crystallisation–degassing (AFCD). The samples are highly vesicular (up to 18%) and the volatiles trapped in vesicles consist predominantly of H₂O with minor amounts of CO₂, and the concentration of water in the glasses indicates that H₂O saturation was attained. Rare gases except helium are atmospheric in origin, and the ³He/⁴He ratios and the CO₂/³He ratios are respectively lower and higher than those typical of Mid-Ocean Ridge Basalt (MORB), and appear to correlate with the degree of differentiation. AFCD allows efficient degassing of mantle-derived volatiles and contribution of crust-derived and atmosphere-derived volatiles. Given the widespread occurrence of differentiated magmatism at arcs, we suggest that AFCD is responsible for large-scale occurrence of ³He-rich crustal fluids and of atmospheric-like rare gases in arc emanations, and that most of the volatiles are lost continuously during fractional crystallisation, rather than catastrophically during eruptions.     

Geographical Distribution of 3He/4He Ratios in the Chugoku District, Southwestern Japan

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 R_atm to 5.04 R_atm (where R_atm 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 R_atm and 3.8±1.6 R_atm, 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.     

Noble gas systematics for coexisting glass and olivine crystals in basalts and dunite xenoliths from Loihi Seamount

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 (R_A), 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 R_A) 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.     

Helium and argon isotopes of the Tertiary basic igneous rocks from Shandong Peninsula and implications for the magma origin

Helium (He) and Argon (Ar) isotopic compositions of the Tertiary basic igneous rocks were determined by the high temperature melting extraction method. The selected samples for the studies included al-kaline basalts and diabases from the Jiyang basin,and the surrounding Shanwang and Qixia outcrops in the Shandong Peninsula,eastern China. The results show that the Paleogene basalts and diabases from the Jiyang basin yielded a wide range of P4 PHe abundance of (73.70-804.16)×10 P-8 Pcm P3 P STP·g P-1 P,with P3 PHe/ P4 PHe ratios of 0.374-2.959 Ra,which was lower than the MORB but evidently higher than the con-tinental crust value. The Neogene alkaline basalts from the Jiyang basin,Shanwang and Qixia outcrops have variable P4 PHe abundances ((42.34-286.72)×10-8 Pcm P3 P STP·g-1 P),and "continental crust-like" P3 PHe/ P4 PHe ratios (0.013-0.074 Ra). All of them contain atmospheric-like P40 PAr/ P36 PAr ratio (395.4-1312.7),reflecting the mantle sources with air components. Their low P3 PHe/ P4 PHe ratios are interpreted as the enrichment of the radiogenic P4 PHe mainly inherited from the mantle. He and Ar systematics show the mixing of MORB-type,air and a P4 PHe enriched member in the mantle source,suggesting that these igneous rocks originated from the depleted asthenospheric mantle mixed with an EMI component. Therefore,the present He and Ar isotopes do not support the viewpoints that the Cenozoic igneous rocks of Eastern North China were the products of mantle plume(s) activities.     

An important source ofHe (andHe) in diamonds

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 R_a (R_a 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.     

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

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

Primordial neon,helium, and hydrogen in oceanic basalts

A primordial neon component in neon from Kilauea Volcano and deep-sea tholeiite glass has been identified by the presence of excess²⁰Ne; relative to atmospheric neon the²⁰Ne enrichments are 5.4% in Kilauea neon and about 2.5% in the basalts. The²⁰Ne anomalies are associated with high³He/⁴He ratios; the ratio in Kilauea helium is 15 times the atmospheric ratio, while mid-ocean ridge basalts from the Atlantic, Pacific, and Red Sea have uniform ratios about 10 times atmospheric. Mantle neon and helium are quite different in isotopic composition from crustal gases, which are highly enriched in radiogenic²¹Ne and⁴He. The²¹Ne/⁴He ratios in crustal gases are consistent with calculated values based on G. Wetherill's¹⁸O (α,n) reaction; the lack of²⁰Ne enrichment in these gases shows that the mantle²⁰Ne anomalies are not radiogenic.²¹Ne enrichments in Kilauea neon and “high-³He” Pacific tholeiites are much less than in crustal neon, about 2 ± 2% vs. present atmospheric neon, as expected from the much lower⁴He/Ne ratios.Neon concentrations in two Atlantic tholeiites were found to be only 1–2% of the values obtained by Dymond and Hogan; helium concentrations are slightly greater and our He/Ne ratios are greater by a factor of 150. The large Ne excess relative to solar wind and meteoritic gases is thus not confirmed. Pacific and Atlantic basalts appear to be quite different in He/Ne ratios however, and He and Ne may be inversely correlated. He concentration variations due to diffusive loss can be distinguished from variations due to two-phase partitioning or mantle heterogeneity by the effects on³He/⁴He ratios. The He isotopic and concentration measurements on “low-³He” basalts are consistent with diffusive loss and dilution of the 3/4 ratio by in-situ radiogenic⁴He, and may provide a method for dating basalt glasses.Deuterium/hydrogen ratios in Atlantic and Pacific tholeiite glasses are 77% lower than the ratio in seawater. The inverse correlation between deuterium and water content observed by Friedman in erupting Kilauea basalts is consistent with a Rayleigh separation process in which magmatic water is separated from an initial melt with the same D/H ratio as observed in deep-sea tholeiites. The consistency of the D/H ratios in tholeiites containing primordial He and Ne components indicates that these ratios are probably characteristic of primordial or juvenile hydrogen in the mantle.     

Complementary use of dating and hydrochemical tools to assess mixing processes involving centenarian groundwater in a geologically complex alpine karst aquifer

Environmental dating tracers (³H, ³He, ⁴He, CFC-12, CFC-11, and SF₆) and the natural spring response (hydrochemistry, water temperature, and hydrodynamics) were jointly used to assess mixing processes and to characterize groundwater flow in a relatively small carbonate aquifer with complex geology in southern Spain. Results evidence a marked karst behaviour of some temporary outlets, with sharp and rapid responses to precipitation events, while some perennial springs show buffer and delayed variations with respect to recharge periods. The general geochemical evolution shows a pattern, from higher to lower altitudes, in which mineralization and the Mg/Ca ratio rise, evidencing longer water–rock interaction. The large SF₆ concentrations in groundwater suggest terrigenic production, whereas CFC-11 values are affected by sorption or degradation. The groundwater age in the perennial springs—as deduced from CFC-12 and ³H/³He—points to mean residence times of several decades, although the large amount of radiogenic ⁴He in samples indicate a contribution of old groundwater (free of ³H and CFC-12). Lumped parameter models and shape-free models were created based on ³H, tritiogenic ³He, CFC-12, and radiogenic ⁴He data in order to interpret the age distribution of the samples. Results evidence the existence of two mixing components, with an old fraction ranging between 160 and 220 years in age. The correlation of physicochemical parameters with some dating parameters, derived from the mixing models, serves to explain the hydrogeochemical processes occurring within the system. Altogether, long residence times are shown to be possible in small alpine systems with a clearly karst behaviour if the geological setting features highly tectonized media including units with diverse hydrogeological characteristics. These findings highlight the importance of applying different approaches, including groundwater dating techniques, when studying such groundwater flow regimes.     

Geochemical monitoring of the 2002–2003 eruption at Stromboli volcano (Italy): precursory changes in the carbon and helium isotopic composition of fumarole gases and thermal waters

Significant changes in the helium and carbon isotopic composition of shallow thermal waters vs. gas and a crater fumarolic gas have been recorded at Stromboli prior and during the 2002–2003 eruption. The³He/⁴He ratios corrected for air contamination (Rc/Ra), and δ¹³C of fumarolic gases gradually increased from May to November 2002 before the eruption onset. These variations imply early degassing of a gas-rich magma at depth that likely fed both the intense Strombolian activity and small lava overflows recorded during that period. The lava effusion of late December 2002 was shortly preceded by a marked Rc/Ra decrease both in water and fumarolic gases. Comparison of He/CO₂ and CH₄/CO₂ ratios in dissolved gas and with values rules out the Rc/Ra decrease due to an increasing input of radiogenic⁴He. The Rc/Ra decrease is attributed to the He isotope fractionation during rapid magma ascent and degassing. A new uprising of ³He-rich magma probably occurred in January to February 2003, when Rc/Ra ratios displayed the highest values in dissolved gases ever measured before (4.56 Rc/Ra). The increase in He/CO₂ and CH₄/CO₂ ratios and decrease in δ¹³C of dissolved CO₂ was recorded after the 5 April 2003 explosive paroxysm, likely caused by enhanced gas-water interaction inducing CO₂ dissolution. No anomalous Rc/Ra values were recorded in the same period, when usual Strombolian activity gradually resumed.Editorial responsibility: H Shinohara     

Helium isotope studies of the mantle xenoliths and megacrysts from the Cenozoic basalts in the eastern China

Helium isotope compositions of the mantle xenoliths and megacrysts in the Cenozoic basalts in the eastern China were measured. The samples were collected from Ludao of Heilongjiang, Huinan and Jiaohe of Jilin, Kuandian of Liaoning, Hannuoba of Hebei, Nüshan of Anhui, Dingan of Hainan. The³He/⁴He ratios of the mantle xenoliths and megacrysts from the most areas were about 1 × 10^-5, and were similar to those of the MORB, thus reflecting the characteristics of the MORB-typed depleted mantle. The³He/⁴He ratios of the mantle xenoliths from Jiaohe were 4.8×10^-6 and the³He/⁴He ratios of xenoliths from Hannuoba vary from 0.15× 10^-6 to 7.4 ×10^-6, obviously lower than those of the MORB, and even lower than the atmospheric helium isotope ratios, indicating that the continental mantle was strongly replaced in Jiaohe and Hannuoba areas. The helium isotope compositions of the mantle xenoliths and megacrysts in the same region vary in a very wide range. It is inferred that the mantle xenoliths and megacrysts were from different parts of the continental mantle. There were not necessary origin relations between the mantle xenoliths, megacrysts and their host basalts. An extremely high³He/⁴He ratio of garnet megacryst from Hannuoba, Hebei was found.     

N<Subscript>2</Subscript>, Ar,and He as a tool for discriminating sources of volcanic fluids with application to Vulcano,Italy

A detailed analysis of published data on the N₂, Ar, and He content and Ar and He isotopic composition of fumarolic fluids from Vulcano crater (south Italy) supports a model with two endmembers comprising magmatic and hydrothermal fluids with correspondingly low and high H₂O content. The magmatic component with the highest ³He/⁴He and highest absolute concentrations of N₂, Ar, and He also has the lowest N₂/Ar and N₂/He ratios (∼300 and ∼500, respectively). In contrast, the hydrothermal endmember, with the lower ³He/⁴He and lower absolute N₂, Ar, and He abundances, has high N₂/Ar (∼1,000) and high N₂/He (>3,000) ratios. The hydrothermal component is also characterized by the highest ⁴⁰Ar/³⁶Ar ratios (>1,000) and is proposed to be the main carrier of metamorphic gases from the arc crust.     

Excess3He in the deep water over the Mid-Atlantic Ridge at 26°N: evidence of hydrothermal activity

We have observed distinct and significant patterns of excess³He in bottom waters over the Mid-Atlantic Ridge in the “TAG hydrothermal field”. The lateral regional gradients are comparable in magnitude to gradients observed in the Galapagos rift, an area of confirmed hydrothermal activity. Together with this, the³He patterns, magnitudes and vertical gradients all indicate on-going and continuous hydrothermal activity.     

Helium isotopic variations in volcanic rocks from Loihi Seamount and the Island of Hawaii

Helium isotopic ratios ranging from 20 to 32 times the atmospheric ³He/⁴He(R_A) 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 R_A), 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 R_A) 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 R_A) 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.     

Geochemistry on mantle-derived volatiles in natural gases from eastern China oil/gas provinces (I)

Commercial accumulation of mantle-derived helium in the sedimentary shell is discussed. Generally speaking, a commercial helium pool is formed by accumulated⁴He that comes from uranium and thorium via α-decay; therefore, it has a very low³He/⁴He value in the magnitude of 10-⁸. The helium concentration in some gas wells of eastern China oil/gas provinces is about or over 0.05% —0. 1%, consequently forming commercial helium wells (pools), such as the Wangjinta Gas Pool in Songliao Basin, Huangqiao Gas Pool in North Jiangsu Basin and some gas wells in Sanshui Basin. Studies have proved that when the³He/⁴He value of a helium gas pool is about 3.7 × 10^-6 -7.2×10^-6 namely mantle-derived helium in its total helium concentration accounts for 33.5%—65.4%, it is a crust-mantle dual-source or dominantly mantle-derived helium gas pool, which is a novel helium resource and its formation is mainly related to the distribution of megafractures.