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1.
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   

2.
Primordial neon,helium, and hydrogen in oceanic basalts   总被引：3，自引：0，他引：3  
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.  相似文献   

3.
We have collected 14 water and gas samples from 9 thermal springs and gas vents near Nevado del Ruiz volcano, Colombia. The 3He/4He and 4He/20Ne ratios vary significantly from 0.98 Ratm (where Ratm is the atmospheric 3He/4He ratio of 1.4 × 10−6) to 6.30 Ratm, and from 0.37 to 7.0, respectively. The 3He/4He ratio (corrected for air contamination) decreases with increasing distance from the central crater of the volcano to the sampling site. The trend is very similar to that observed at Ontake volcano, Japan. A hydrodynamic porous-media dispersion model can explain the 3He/4He trend. The temporal variations in the 3He/4He ratio at four sites provide useful information on the apparent velocity of the magmatic fluid flow brought on by a volcanic eruption. The estimated value of several tens m day−1 agrees well with the inferred velocity of flow in Oshima volcano, Japan and is comparable to the largest rate of groundwater movement in a deep sedimentary basin.  相似文献   

4.
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   

5.
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   

6.
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.  相似文献   

7.
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   

8.
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.  相似文献   

9.
Using classical diffusion theory, we present a mathematical technique for the determination of 4He concentration profiles in minerals. This approach should prove useful for constraining the low-temperature cooling histories of individual samples and for correcting (U–Th)/He ages for partial diffusive loss. The calculation assumes that the mineral of interest contains an artificially produced and uniform distribution of 3He obtained by proton irradiation [Shuster et al., Earth Planet. Sci. Lett. 217 (2004) 19–32]. In minerals devoid of natural helium, this isotope allows measurement of He diffusion coefficients; in minerals with measurable radiogenic He, it permits determination of 4He profiles arising during ingrowth and diffusion in nature. The 4He profile can be extracted from stepwise degassing experiments in which the 4He/3He ratio is measured. The evolution of the 4He/3He ratio as a function of cumulative 3He released can be compared with forward models to constrain the shape of the profile. Alternatively, we present a linear inversion that can be used to directly solve for the unknown 4He distribution. The inversion incorporates a standard regularization technique to filter the influence of random measurement errors on the solution. Using either approach we show that stepwise degassing data can yield robust and high-resolution information on the 4He profile. Profiles of radiogenic He are a sensitive function of the time–Temperate (t–T) path that a cooling sample experienced. Thus, by step heating a proton-irradiated sample it is possible to restrict the sample’s acceptable t–T paths. The sensitivity of this approach was explored by forward-modeling 4He profiles resulting from a range of realistic t–T paths, using apatite as an example. Results indicate that 4He profiles provide rich information on t–T paths, especially when the profiles are coupled with (U–Th)/He cooling ages on the same sample. Samples that experienced only moderate diffusive loss have 4He concentration profiles that are rounded at the edge but uniform in the core of the diffusion domain. Such profiles can be identified by nearly invariant 4He/3He ratios after the first few to few tens of percent of 3He have been extracted by step heating. We show how such data can be used to correct (U–Th)/He ages for partial diffusive loss.  相似文献   

10.
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   

11.
Cosmogenic 3He can be used to date a wide range of mineral phases because it is produced from all target elements and can be readily measured above atmospheric contamination. Calcite is a particularly attractive target mineral due to its natural abundance, large crystal size (>1 mm), and low He closure temperature (<70 °C), which limit non-cosmogenic 3He components (Copeland et al., 2007). However, several recent studies have shown that some calcite may not be retentive to helium, even under surface temperatures (Cros et al., 2014; Copeland et al., 2007). This study thus explores 3He retention and production in natural calcite samples at four different sites. Samples from two high elevation sites appear retentive to 3He over 10 kyr timescales, whereas two additional sites clearly suffer from diffusive loss of 3He. Step-degassing experiments suggest that diffusion in calcite is controlled by multiple diffusion domains, with an apparent activation energy of 25–27 kcal mol−1. Although minor 3He loss is expected from the smallest diffusion domains, the observed kinetics cannot explain the poor retention at all sites. We thus propose that opaque (non-transparent) calcite may be more retentive due to the presence of imperfections in the crystal lattice. We conclude that 3He dating of calcite shows promise in some settings. However, because retention depends on crystallographic variability it must be evaluated on a case-by-case basis until robust criteria for retention can be identified.  相似文献   

12.
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   

13.
Berlin relies on induced bank filtration from a broad‐scale, lake‐type surface water system. Because the surface water contains treated sewage, wastewater residues are present in surface water and groundwater. Multiple environmental tracers, including tritium and helium isotopes (3H, 3He, 4He), stable isotopes (δ18O and δ2H) and a number of persistent sewage indicators, such as chloride, boron and a selection of pharmaceutical residues (phenazone‐type analgesics and their metabolites, carbamazepine and anthropogenic gadolinium, Gdexcess), were used to estimate travel times from the surface water to individual production and observation wells at two sites. The study revealed a strong vertical age stratification throughout the upper aquifer, with travel times varying from a few months to several decades in greater depth. Whereas the shallow bank filtrate is characterized by the reflection of the time‐variant tracer input concentrations and young 3H/3He ages, the deeper, older bank filtrate displays no tracer seasonality, 3H/3He ages of a few years to decades and strongly deviating concentrations of several pharmaceutical residues, reflecting concentrations of the source surface water over time. The phenazone‐type pharmaceuticals persist in the aquatic environments for decades. Bank filtration in Berlin is only possible at the sandy lakeshores. In greater water depth, impermeable lacustrine sapropels inhibit infiltration. The young bank filtrate originates from the nearest shore, whereas the older bank filtrate infiltrates at more distant shores. This paper illustrates the importance of using multiple tracer methods, capable of resolving a broad range of residence times, to gain a comprehensive understanding of time‐scales and infiltration characteristics in a bank filtration system. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

14.
To investigate the isotopic composition and age of water in volcanic gases and magmas, we analyzed samples from 11 active volcanoes ranging in composition from tholeiitic basalt to rhyolite: Mount St. Helens (USA), Kilauea (USA), Pacaya (Guatemala), Galeras (Colombia), Satsuma Iwo-Jima (Japan), Sierra Negra and Alcedo (Ecuador), Vulcano (Italy), Parícutin (Mexico), Kudryavy (Russia), and White Island (New Zealand). Tritium at relatively low levels (0.1–5 T.U.) is found in most emissions from high-temperature volcanic fumaroles sampled, even at discharge temperatures >700°C. Although magmatic fluids sampled from these emissions usually contain high CO2, Stotal, HCl, HF, B, Br, 3He R/RA, and low contents of air components, stable isotope and tritium relations of nearly all such fluids show mixing of magmatic volatiles with relatively young meteoric water (model ages≤75 y). Linear δD/δ18O and 3H/δ18O mixing trends of these two end-members are invariably detected at arc volcanoes. Tritium is also detected in fumarole condensates at hot spot basalt volcanoes, but collecting samples approaching the composition of end-member magmatic fluid is exceedingly difficult. In situ production of 3H, mostly from spontaneous fission of 238U in magmas is calculated to be <0.001 T.U., except for the most evolved compositions (high U, Th, and Li and low H2O contents). These values are below the detection limit of 3H by conventional analytical techniques (about 0.01 T.U. at best). We found no conclusive evidence that natural fusion in the Earth produces anomalous amounts of detectable 3H (>0.05 T.U.).  相似文献   

15.
Radial transport theory for inner radiation zone MeV ions has been extended by combining radial diffusive transport and losses due to Coulomb friction with local generation of D, T and 3He ions from nuclear reactions taking place on the inner edge of the inner radiation zone. Based on interactions between high energy trapped protons and upper atmospheric constituents we have included a nuclear reaction yield D, T and 3He flux source that was numerically derived from a nuclear reaction model code originally developed at the Institute of Nuclear Researches in Moscow, Russia. Magnetospheric transport computations have been made covering the L-shell range L=1.0–1.6. The resulting MeV energy D, T and 3He ion flux distributions show a strong influence of the local nuclear source mechanism on the inner zone energetic D, T and 3He ion content.  相似文献   

16.
The purpose of this work is to refine our knowledge about the nature of helium with a high abundance of the rare isotope3He(3He/4He= 10?5) discovered in terrestrial volcanic gases in 1968.We will discuss here the results of isotope analyses of helium released by step-wise heating of ultrabasic xenoliths and some volcanic rocks. On the basis of these results, possible sources of3He in the earth due to fission and nuclear reactions are considered critically. The most probable source of the high abundance of3He is shown to be due to the capture and trapping of primordial He by the earth during its formation (primordial helium3He/4He= 3 × 10?4), a small but significant fraction of which has been retained to the present time.  相似文献   

17.
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.  相似文献   

18.
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   

19.
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   

20.
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   

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