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1.
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   

2.
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   

3.
Helium, neon and argon isotope compositions of fluid inclusions have been measured in hydrothermal sulfide samples from the TAG hydrothermal field at the Mid-Atlantic Ridge. Fluid-inclusion3He/4He ratios are 2.2—13.3 times the air value (Ra), and with a mean of 7.2 Ra. Comparison with the local vent fluids (3He/4He=7.5—8.2 Ra) and mid-ocean ridge basalt values (3He/4He=6—11 Ra) shows that the variation range of3He/4He ratios from sulfide-hosted fluid inclusions is significantly large. Values for20Ne/22Ne are from 10.2 to 11.4, which are significantly higher than the atmospheric ratio (9.8). And fluid-inclusion40Ar/36Ar ratios range from 287 to 359, which are close to the atmospheric values (295.5). These results indicate that the noble gases of fluid inclusions in hydrothermal sulfides are a mixture of mantle- and seawater-derived noble gases; the partial mantle-derived components of trapped hydrothermal fluids may be from the lower mantle; the helium of fluid inclusions is mainly from upper mantle; and the Ne and Ar components are mainly from seawater.  相似文献   

4.
The isotopic composition and abundances of He, Ne and Ar have been measured in a sequence of vertically stacked gas reservoirs at Hajduszoboszlo and Ebes, in the Pannonian Basin of Hungary. The gas reservoirs occur at depths ranging from 727 to 1331 m, are CH4 dominated and occupy a total rock volume of approximately 1.5 km3. There are systematic variations in both major species abundances and rare gas isotopic composition with depth: CO2 and N2 both increase from 0.47 and 1.76% to 14.1 and 30.5%, respectively, and 40Ar/36Ar and 21Ne/22Ne increase systematically from 340 and 0.02990 at 727 m to 1680 and 0.04290 at 1331 m. A mantle-derived He component between 2 and 5% is present in all samples, the remainder is crustal-radiogenic He. The Ar and Ne isotope variations arise from mixing between atmosphere-derived components in groundwater, and crustally produced radiogenic Ar and Ne. The atmosphere-derived 40Ar and 21Ne decreases from 85 and 97% of the total 40Ar and 21Ne at 727 m to 18 and 68% at 1331 m. The deepest samples are shown to have both atmosphere-derived and radiogenic components close to the air-saturated water and radiogenic production ratios. The shallowest samples show significant fractionation of He/Ar and Ne/Ar ratios in atmosphere-derived and radiogenic rare gas components, but little or no fractionation of He/Ne ratios. This suggests that diffusive fractionation of rare gases is relatively unimportant and that rare gas solubility partitioning between CH4 and H2O phases controls the observed rare gas elemental abundances.The total abundance of atmosphere-derived and radiogenic rare gas components in the Hajduszoboszlo gas field place limits on the minimum volume of groundwater that has interacted with the natural gas, and the amount of crust that has degassed and supplied radiogenic rare gases. The radiogenic mass balance cannot be accounted for by steady state production either within the basin sediments or the basement complex since basin formation. The results require that radiogenic rare gases are stored at their production ratios on a regional scale and transported to the near surface with minimal fractionation. The minimum volume of groundwater required to supply the atmosphere-derived rare gases would occupy a rock volume of some 1000 km3 (assuming an average basin porosity of 5%), a factor of 670 greater than the reservoir volume. Interactions between groundwater and the Hajduszoboszlo hydrocarbons has been on a greater scale than often envisaged in models of hydrocarbon formation and migration.  相似文献   

5.
This study presents new major and trace element, mineral, and Sr, Nd, and noble gas isotope geochemical analyses of basalts, gabbro, and clinopyroxenite from the Mariana Arc (Central Islands and Southern Seamount provinces) including the forearc, and the Mariana Trough (Central Graben and Spreading Ridge). Mantle source compositions beneath the Mariana Arc and the Mariana Trough indicate a mantle source that is depleted in high field strength elements relative to MORB (mid‐oceanic ridge basalt). Samples from the Mariana Arc, characterized by high ratios of Ba/Th, U/Th, 84Kr/4He and 132Xe/4He, are explained by addition of fluid from the subducted slab to the mantle wedge. Correlations of noble gas data, as well as large ion lithophile elements, indicate that heavy noble gases (Ar, Kr, and Xe) provide evidence for fluid fluxing into the mantle wedge. On the other hand, major elements and Sr, Nd, He, and Ne isotopic data of basalts from the Mariana Trough are geochemically indistinguishable from MORB. Correlations of 3He/4He and 40Ar/36Ar in the Mariana Trough samples are explained by mixing between MORB and atmosphere. One sample from the Central Graben indicates extreme enrichment in 20Ne/22Ne and 21Ne/22Ne, suggesting incorporation of solar‐type Ne in the magma source. Excess 129Xe is also observed in this sample suggesting primordial noble gases in the mantle source. The Mariana Trough basalts indicate that both fluid and sediment components contributed to the basalts, with slab‐derived fluids dominating beneath the Spreading Ridge, and that sediment melts, characterized by high La/Sm and relatively low U/Th and Zr/Nb, dominate in the source region of basalts from the Central Graben.  相似文献   

6.
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   

7.
We performed a complete noble gas study on eight different josephinites and one oregonite. The 4He/3He ratios range between 100,000 and 330,000 and are probably due to a combination of a MORB He-component from the Josephinite Peridotite massif, where these nickel-iron specimens are found, and either atmospheric He or radiogenic He from the underlying continental or subcontinental basement. The 40Ar/36Ar ratios of 302 to 381 are slightly higher than the ratio of air-argon. The neon, krypton and xenon isotopic ratios are identical to the corresponding air ratios. We cannot confirm large3He and21Ne excesses published earlier. The observed noble gas isotopic signatures are in agreement with a formation of josephinites near the surface. The data do not favour a deep mantle origin or a formation at the mantle-core boundary as proposed before.  相似文献   

8.
All twenty-three stable rare gas isotopes have been measured in a mantle-derived amphibole, kaersutite. The elemental abundance pattern of the rare gases is similar to the “planetary” rare gas pattern as defined by carbonaceous chondrites. The3He/4He ratio, (4.9 ± 0.6) × 10?5, is suggestive of primordial He degassing from the mantle. Excess21Ne is present. The measured40Ar/36Ar ratio,400 ± 5, may represent a mantle40Ar/36Ar ratio <240 when corrected for radiogenic40Ar. The heavy isotopes of Kr and t0he Xe isotopes are within error of the atmosphere values.  相似文献   

9.

In the Tarim Basin, black shale series at the bottom of Cambrian is one of the important marine facies hydrocarbon source rocks. This research focuses on the analysis of the isotope of noble gas of 11 cherts. The R/R a ratio of chert in the Keping area is 0.032–0.319, and 40Ar/36Ar is 338–430. In Quruqtagh the R/R a ratio is 0.44–10.21, and 40Ar/36Ar is 360–765. The R/R a ratio of chert increases with 40Ar/36Ar from the west to the east accordingly. They have evolved from the crust source area to the mantle source area in a direct proportion. Surplus argon 40ArE in chert is in direct proportion to the R/R a ratio, indicating that it has the same origin of excess argon as in fluid and mantle source helium. Comparison of the R/R a ratios between the west and the east shows that the chert in the eastern part formed from the activity system of the bottom hydrothermal venting driven by the mantle source, where the material and energy of crust and mantle had a strong interaction in exchange; whereas in the western part, chert deposited from the floating of hydrothermal plume undersea bottom, which is far away from the centre of activities of the hydrothermal fluid of ocean bottom. In addition, from noble gas isotope composition of chert, it is suggested that the ocean anoxia incident happened at the black shale of the Cambrian bottom probably because of the large-scaled ocean volcanoes and the following hydrothermal activities.

  相似文献   

10.
Abundances and isotopic compositions of all the stable noble gases have been measured in 19 different depths of the Apollo 15 deep drill core, 7 different depths of the Apollo 16 deep drill core, and in several surface fines and breccias. All samples analyzed from both drill cores contain large concentrations of solar wind implanted gases, which demonstrates that even the deepest layers of both cores have experienced a lunar surface history. For the Apollo 15 core samples, trapped4He concentrations are constant to within a factor of two; elemental ratios show even greater similarities with mean values of4He/22Ne= 683±44,22Ne/36Ar= 0.439±0.057,36Ar/84Kr= 1.60±0.11·103, and84Kr/132Xe= 5.92±0.74. Apollo 16 core samples show distinctly lower4He contents,4He/22Ne(567±74), and22Ne/36Ar(0.229±0.024), but their heavy-element ratios are essentially identical to Apollo 15 core samples. Apollo 16 surface fines also show lower values of4He/22Ne and22Ne/36Ar. This phenomenon is attributed to greater fractionation during gas loss because of the higher plagioclase contents of Apollo 16 fines. Of these four elemental ratios as measured in both cores, only the22Ne/36Ar for the Apollo 15 core shows an apparent depth dependance. No unambiguous evidence was seen in these core materials of appreciable variations in the composition of the solar wind. Calculated concentrations of cosmic ray-produced21Ne,80Kr, and126Xe for the Apollo 15 core showed nearly flat (within a factor of two) depth profiles, but with smaller random concentration variations over depths of a few cm. These data are not consistent with a short-term core accretion model from non-irradiated regolith. The Apollo 15 core data are consistent with a combined accretion plus static time of a few hundred million years, and also indicate variable pre-accretion irradiation of core material. The lack of large variations in solar wind gas contents across core layers is also consistent with appreciable pre-accretion irradiation. Depth profiles of cosmogenic gases in the Apollo 16 core show considerably larger concentrations of cosmogenic gases below ～65 cm depth than above. This pattern may be interpreted either as an accretionary process, or by a more recent deposition of regolith to the upper ～70 cm of the core. Cosmogenic gas concentrations of several Apollo 16 fines and breccias are consistent with ages of North Ray Crater and South Ray Crater of ～50·106 and ～2·106 yr, respectively.  相似文献   

11.
Cosmogenic 21Ne was utilised to determine exposure ages of young subaerial basaltic lava flows from the Newer Volcanic Province, western Victoria, Australia. The ages (36–53 ka) determined from co-existing cosmogenic 21Ne and 3He in olivines separated from basalts are consistent within analytical uncertainties with ages previously determined by cosmogenic 36Cl exposure dating. This paper illustrates the potential of cosmogenic neon exposure ages in studying the eruption, surface morphology, and erosion history of young volcanic rocks, which are difficult to date using other conventional methods, such as K-Ar or 40Ar/39Ar dating. The present study demonstrates that combined cosmogenic 3He and 21Ne dating, specifically measured cosmogenic 3He/21Ne ratios, on the same samples, is powerful for evaluating the validity of calculated cosmogenic 3He and 21Ne surface exposure ages.  相似文献   

12.
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   

13.
Vesicle characteristics (vesicularity, largest vesicle size, number of vesicles/cm2), CO2-δ13C and CO2-4He-40Ar-40Ar/36Ar in vesicles and CO2-δ13C in the glass have been measured in 19 tholeiitic basalt glasses from the Easter Microplate East Ridge (East Pacific Rise) collected at 3 different sites (26°S East Ridge, Pito Seamount and Pito Deep at 23°S).Carbon supersaturation values (Cmelt/Csolubility) vary from 1.3 to 4.3. Carbon supersaturation values are strongly correlated with the number of vesicles/cm2. There is also a correlation between number of vesicles/cm2 and vesicle size. At the Pito Seamount site, there is a negative correlation between carbon supersaturation values and observed carbon isotope fractionation between CO2 in vesicles and carbon dissolved in the glass (Δ13Cobserved). High 4He/40Ar* ratios in vesicles (from 49 to 190) are observed in both the most and least carbon supersaturated samples, while samples with intermediate carbon supersaturation have the lowest 4He/40Ar* ratios (16±1). These correlations show that most quenched melts record different disequilibrium to equilibrium states during closed-system degassing.The samples showing the highest carbon supersaturation (4.3) have the highest 4He/40Ar* (from 94 to 190). This observation shows for the first time that the 4He/40Ar* ratio can be kinetically fractionated during incomplete degassing of magmas from the magma chamber to the seafloor. This result implies that high 4He/40Ar* ratios are not a systematic indicator of open-system degassing (Rayleigh distillation) and that caution should be taken when using this ratio for any degassing correction.A two-stage degassing model, with the first stage being a closed-system degassing occurring between the source and the magma chamber, and the second stage of degassing (with a mode varying from open-system degassing to different degrees of kinetic closed-system degassing) taking place between the magma chamber and eruption on the seafloor, is the most appropriate to describe the degassing of MORB. Reconstructing initial carbon content of the magma prior to degassing and extrapolating the results to the entire ridge system results in a carbon flux of 1.6-0.3+0.6×1014 g/year. This value implies vigorous exchange of carbon between the mantle and the surface throughout geological times.  相似文献   

14.
The chronology and origin of volcanism of Ascension Island, South Atlantic Ocean, is poorly resolved. Here we use in situ produced cosmogenic 3He in olivine and pyroxene phenocrysts from well-preserved lava flows to date the main sub-aerial basalt volcanism on the island. Etching olivine separates in HF/HNO3 appears to remove a significant proportion of the implanted radiogenic 4He contribution. Average exposure ages of each flow corrected for radiogenic He range from 328 ka to 186 ka and are used to refine the chronology and stratigraphy of the island. Magmatic 3He/4He ratios derived from in vacuo crushing are in the range of 6.3–7.3 RA. This range is lower than the neighbouring Mid-Atlantic Ridge segment (6–8°S) but slightly higher than measured in regional ocean islands of St. Helena, Tristan da Cunha and Gough. Combining these data with new trace element data and published radiogenic isotope ratios it appears that the Ascension Island magmatism is a mix of HIMU mantle material, typified by basalts from St. Helena, and depleted MORB-source mantle.  相似文献   

15.
The geochemical characteristics of mildly alkalic basalts (24–25 Ma) erupted in the southeastern Kerguelen Archipelago are considered to represent the best estimate for the composition of the enriched Kerguelen plume end-member. A recent study of picrites and high-MgO basalts from this part of the archipelago highlighted the Pb and Hf isotopic variations and suggested the presence of mantle heterogeneities within the Kerguelen plume itself. We present new helium and neon isotopic compositions for olivines from these picrites and high-MgO basalts (6–17 wt.% MgO) both to constrain the enriched composition of the Kerguelen plume and to determine the origin of isotopic heterogeneities involved in the genesis of Kerguelen plume-related basalts. The olivine phenocrysts have extremely variable 4He / 3He compositions between MORB and primitive values observed in OIB (∼90,000 to 40,000; i.e., R / Ra ∼8 to 18) and they show primitive neon isotopic ratios (average 21Ne / 21Neext ∼0.044). The neon isotopic systematics and the 4He / 3He ratios that are lower than MORB values for the Kerguelen basalts clearly suggest that the Kerguelen hotspot belongs to the family of primitive hotspots, such as Iceland and Hawaii. The rare gas signature for the Kerguelen samples, intermediate between MORB and solar, is apparently inconsistent with mixing of a primitive component with a MORB-like source, but may result from sampling a heterogeneous part of the mantle with solar 3He / 22Ne and with a higher (U, Th) / 3He ratio compared to typically high R / Ra hotspot basalts such as those from Iceland and Hawaii.  相似文献   

16.
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   

17.
Stepwise heating experiments on separated graphite-diamond-kamacite aggregates have revealed a pronounced difference in the release patterns of spallogenic3He and trapped gases. About half the3He is released at T ? 920°C, without being accompanied by significant amounts of primordial gases; the latter, together with the remaining3He, is given off only at T ? 1200°C. Acid treatment of an aliquant dissolved about 2/3 of the total Fe in the sample but did not cause a significant change in the gas concentrations. It is concluded that (a) there is no evidence for a loss of spallogenic3He from the graphite-diamond-kamacite aggregates, (b) one major constituent of the aggregates - graphite - is almost void of trapped gases, (c) kamacite is not a main carrier of the gases. This leaves diamond as the most probable site of the primordial gases.The elemental abundance pattern in the noble gases is essentially as reported previously. In particular, the excellent correlation between relative depletion factors, normalized to the cosmic abundance ratios, and the respective ionisation energies is confirmed. Other important features of the trapped gases are a20Ne/22Ne ratio of 12.3 ± 0.6, intermediate between solar wind and solar flare implanted Ne,36Ar/38Ar = 5.20 ± 0.06 and a measured40Ar/36Ar ratio (before blank correction) of 0.0076.Possible modes of trapping of the noble gases are discussed.  相似文献   

18.
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.  相似文献   

19.
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.  相似文献   

20.
Cores and coats of five coated diamonds, one from Botswana and four from Zaire, were separately analyzed for their noble gases. Noble gases in the diamonds are essentially of a trapped origin, including radio- and nucleogenic components such as4He, 40Ar, 21Neexcess and excesses in Xe isotopes (129, 131–136). The fairly precise elemental and isotopic abundances allow us to infer the noble gas state in the ancient mantle. 20Ne/22Ne ratios are fairly constant (11.8 ± 0.4), and very close to that of SEP (solar energetic particle)-Ne, but distinctly different from the atmospheric ratio. 21Ne/22Ne ratios range from 0.028 to 0.06, which is attributed to nucleogenic 21Ne from 18O(α, n)21Ne and 24Mg(n, α)21Ne reactions. The difference in 20Ne/22Ne between atmosphere and mantle can be attributed to the hydrodynamic escape of hydrogen from the primitive atmosphere during the very early stage in the Earth's history. 38Ar/36Ar and Kr isotopic ratios are identical to the atmospheric values within 1%. After correction for 238U- or 244Pu-fission Xe, the 131–136Xe abundance ratios are indistinguishable from atmospheric ratios. Lighter Xe isotopes (124–128Xe) are also likely to be atmospheric, but a final conclusion must wait until better data are obtained.In a 136Xe/130Xe−129Xe/130Xe diagram, diamond data lie on the same line as defined for MORB. The observed identical correlation for both diamonds and MORB's appears to suggest that the progenitor of the excess131–136Xe is 244Pu, but not238U, though the direct Xe isotopic measurements was not precies enough to decide unanimously the progenitor.  相似文献   

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