首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
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.  相似文献   

2.
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   

3.
Rare gas isotopes in a phlogopite nodule and a phlogopite-bearing peridotite nodule in South African kimberlites were studied to examine the state of rare gases in the deep interior of the kimberlite region.Within the experimental error of 1 ～ 2%, rare gas isotopic compositions are atmospheric except for radiogenic4He and40Ar. No excess129Xe was observed.In phlogopite, Ne is more depleted, whereas the heavier rare gases are more enriched than the atmospheric rare gases relative to36Ar.Together with other data these results suggest that the state of rare gases in the upper mantle of the South African kimberlite region might have been changed from the typical primitive mantle by a process such as mixing of crustal materials.  相似文献   

4.
A redetermination of the isotopic composition of atmospheric argon by Lee, J.-Y., Marti, K., Severinghaus, J.P., Kawamura, K., Yoo, H.-S., Lee, J.B., Kim, J.S. [2006. A redetermination of the isotopic abundances of atmospheric Ar. Geochimica et Cosmochimica Acta 70, 4507–4512] represents the first refinement since the work of Nier [1950. A redetermination of the relative abundances of the isotopes of carbon, nitrogen, oxygen, argon, and potassium. Physical Reviews 77, 789–793]. The new 40Ar:38Ar:36Ar proportions imply <1% adjustments to 40Ar/39Ar ages in all but exceptional cases of very young and/or K-poor and/or Ca-rich samples, or cases in which samples are grossly under- or over-irradiated. Analytical protocols employing atmospheric argon to determine mass discrimination corrections are insensitive to the effects of revision on the air correction, but are subject to non-negligible adjustments arising from expanded heavy to light isotope ratios attending the increased mass discrimination correction. The competing effects of increased 40Ar/39Ar and 40Ar/37Ar ratios render the adjustments a function of sample chemistry and neutron irradiation parameters. The improved precision of atmospheric 40Ar/36Ar and 38Ar/36Ar permits increasingly sensitive detection of departures from atmospheric values. Non-atmospheric initial 40Ar/36Ar values are increasingly well-documented in volcanic materials, including subatmospheric values correlated with 38Ar/36Ar in a trend consistent with kinetic mass fractionation whereby incomplete equilibration between magma and atmosphere favors light isotope enrichment in the magma. The detailed mechanism(s) of such fractionation are unclear and must be clarified by further study. A detectable increase in atmospheric 40Ar/36Ar in the past 800 ka [Bender, M.L., Barnett, B., Dreyfus, G., Jouzel, J., Porcelli, D., 2008. The contemporary degassing rate of 40Ar from the Earth. Proceedings of the National Academy of Sciences 105, 8232–8237] suggests that ages of late Quaternary (e.g., <100 ka) materials incorporating large amounts of atmospheric argon such as biotite may be underestimated by as much as 100% if a modern atmospheric 40Ar/36Ar value is erroneously assumed, unless air argon is used to determine mass discrimination. Further evaluation of the evolution of paleoatmospheric 40Ar/36Ar, and the fidelity with which argon trapped in igneous materials reflects this, would be very productive. The use of isochrons rather than model (e.g., plateau) ages mitigates the vagaries associated with uncertain trapped argon isotope ratios, and the importance of strategies to derive statistically valid isochrons is underscored.  相似文献   

5.
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   

6.
He, Ne, and Ar have been measured in seven iron meteorites for which anomalous Ag isotopic compositions were reported, in order to determine if107Ag excesses could be related to galactic cosmic-ray bombardment of these meteorites. Our results show that no correlation exists between107Ag excess and either the fluence or the energy spectrum of the particles producing spallogenic rare gases. Cosmic-ray-produced107Ag estimated from38Ar concentrations can account for only about 1% of the observed excess. Elimination of cosmic-ray bombardment as a production mechanism for107Ag excess strengthens the conclusion that the excess107Ag is the decay product of short-lived107Pd (τ1/2=6.5Myr). The iron meteorite Pin?on is shown to contain trapped rare gases with4He/20Ne～600.  相似文献   

7.
YASUO  IKEDA  KEISUKE  NAGAO  ROBERT J.  STERN  MAKOTO  YUASA & SALLY  NEWMAN 《Island Arc》1998,7(3):471-478
Noble gas concentrations and isotopic compositions have been measured in eight samples of pillow basalt glasses collected from seven different localities along 250 km of the Mariana Trough spreading and rifting axis. The samples have uniform and mid-ocean ridge basalt (MORB)-like 3He/4He values of 9–12 × 10–6 (6.4–8.6 times atmospheric) despite large variations in 4He. Concentrations of the noble gases Ne, Ar, Kr, and Xe show much smaller variations between samples, but larger variations in isotopic compositions of Ne, Ar, and Xe. Excess radiogenic 21Ne is observed in some samples. 40Ar/36Ar varies widely (atmospheric to 1880). Kr is atmospheric in composition for all samples. Some samples show a clear excess 129Xe, which is a well-known MORB signature. Isotopic compositions of the heavier noble gases (Ar, Kr, and Xe) in some samples, however, show more atmospheric components. These data reflect the interaction of a MORB-like magma with an atmospheric component such as seawater or of a depleted mantle source with a water-rich component that was probably derived from the subducting slab.  相似文献   

8.
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   

9.
Current research efforts to explore and account for the distribution of nitrogen isotope abundances in the ancient and present-day solar wind and in meteorites often require measurement of nitrogen abundances and isotopic compositions in very small samples of rare extraterrestrial materials. Isotopic analysis of ～ 1 μg of N2 is possible with modern techniques of dynamic mass spectrometry, but even this high sensitivity is a limiting factor for certain critical samples. We have utilized a statistically operated mass spectrometer coupled to an ultrahigh vacuum gas extraction and processing system to lower this limit by approximately four orders of magnitude. Quantities of N2 ranging from ～ 100 ng to < 100 pg are measurable with permil to percent precision in isotope ratios. Nitrogen and all noble gases evolved during stepwise combustion of fine-grained matrix material separated from the Allende meteorite have been meausred simultaneously in a pilot experiment using this technique. Isotopically heavy H-Xe (CCF-Xe) and isotopically light N are co-sited in a carbonaceous carrier phase, supporting a nucleosynthetic origin for15N-depleted nitrogen in Allende. The great isotopic uniformity of trapped Ar in all carrier phases indicates that simple, physical mass fractionation in gravitational escape of volatiles from the primitive nebula cannot have played a significant role in generating the nitrogen compositions observed in solar system matter.  相似文献   

10.
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   

11.
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   

12.
Atmospheric noble gases (e.g., 22Ne, 36Ar, 84Kr, 130Xe) in crustal fluids are only sensitive to subsurface physical processes. In particular, depletion of atmospheric noble gases in groundwater due to boiling and steam separation is indicative of the occurrence of a thermal event and can thus be used to trace the thermal history of stable tectonic regions. We present noble gas concentrations of 38 deep brines (~ 0.5–3.6 km) from the Michigan Basin. The atmospheric noble gas component shows a strong depletion pattern with respect to air saturated water. Depletion of lighter gases (22Ne and 36Ar) is stronger compared to the heavier ones (84Kr and 130Xe). To understand the mechanisms responsible for this overall atmospheric noble gas depletion, phase interaction models were tested. We show that this atmospheric noble gas depletion pattern is best explained by a model involving subsurface boiling and steam separation, and thus, consistent with the occurrence of a past thermal event of mantle origin as previously indicated by both high 4He/heat flux ratios and the presence of primordial mantle He and Ne signatures in the basin. Such a conceptual model is also consistent with the presence of past elevated temperatures in the Michigan Basin (e.g., ~ 80–260 °C) at shallow depths as suggested by previous thermal studies in the basin. We suggest that recent reactivation of the ancient mid-continent rift system underneath the Michigan Basin is likely responsible for the release of both heat and mantle noble gases into the basin via deep-seated faults and fracture zones. Relative enrichment of atmospheric Kr and Xe with respect to Ar is also observed, and is interpreted as reflecting the addition of sedimentary Kr and Xe from associated hydrocarbons, following the hydrothermal event. This study pioneers the use of atmospheric noble gases in subsurface fluids to trace the thermal history of stable tectonic regions.  相似文献   

13.
Analysis of nitrogen and light noble gases in a large sample of glass (lithology C) from the antarctic shergottite EETA 79001 yields a minimumδ15N > +300‰ for the isotopic composition of nitrogen trapped in the glass. The new data fall on the mixing line through the martian atmospheric composition defined byδ15N vs.40Ar/14N for two smaller samples analyzed previously. The results from all three samples are consistent with a two-component nitrogen system in which 84 ppb of trapped martian atmospheric N is mixed in variable proportions with another, more thermally labile N component during stepped heating. This second component, which appears to be indigenous to the glass rather than adsorbed from air and is present in amounts that vary by more than a factor of 3 from sample to sample, may represent volatiles from the martian interior. Data from crystalline phases of several SNC meteorites indicate that the indigenous gas may haveδ15N < −35‰ and36Ar/14N 3 × 10−6, similar to the enstatite chondrites.Neon compositions in EETA 79001 glass samples suggest an earth-like value of 10.1 ± 0.7 for the unknown20Ne/22Ne ratio in the martian atmosphere. The nitrogen-argon correlation systematics yield trapped40Ar/36Ar= 2260 ± 200, within error of the Viking value. There is evidence that36Ar/38Ar in the martian atmosphere is4.1 ± 0.2, strikingly different from terrestrial or typical chondritic ratios near 5.3. Attribution of this low value to excess38Ar generated over martian history by galactic cosmic-ray (GCR) spallation of surface materials would be difficult for a number of reasons, among them the excessive GCR fluences required and the absence of a corresponding21Ne excess.  相似文献   

14.
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   

15.
Fifteen submarine glasses from the East Pacific Rise (CYAMEX), the Kyushu-Palau Ridge (DSDP Leg 59) and the Nauru Basin (DSDP Leg 61) were analysed for noble gas contents and isotopic ratios. Both the East Pacific Rise and Kyushu-Palau Ridge samples showed Ne excess relative to Ar and a monotonic decrease from Xe to Ar when compared with air noble gas abundance. This characteristic noble gas abundance pattern (type 2, classified by Ozima and Alexander) is interpreted to be due to a two-stage degassing from a noble gas reservoir with originally atmospheric abundance. In the Kyushu-Palau Ridge sample, noble gases are nearly ten times more abundant than in the East Pacific Rise samples. This may be attributed to an oceanic crust contamination in the former mantle source.There is no correlation between the He content and that of the other noble gas in the CYAMEX samples. This suggests that He was derived from a larger region, independent from the other noble gases.Except where radiogenic isotopes are involved, all other noble gas isotopic ratios were indistinguishable from air noble gas isotopic ratios. The3He/4He in the East Pacific Rise shows a remarkably uniform ratio of (1.21±0.07)×10?5, while the40Ar/36Ar ranges from 700 to 5600.  相似文献   

16.
Extrusion ages of archaeological obsidian, especially as determined by the 40Ar/39Ar method, can provide reliable maximum ages for tool manufacture. In at least one case in the Middle Awash of Ethiopia, freshly extruded obsidian was used for tool making, resulting in useful maximum ages for site occupation. Hydration resulting in mobility of K and/or Ar in glass, and recoil artifacts produced by neutron irradiation, fatally affect most glass shards from volcanic ashes. The much lower surface area to volume ratio of most archaeological obsidian, however, indicates that the affected areas can be manually removed prior to analysis and the recoil and hydration problems can be easily overcome. A more important issue in dating obsidian is that of possible mass-dependent kinetic isotope fractionation during or subsequent to quenching of volcanic glasses. This is evidenced in some cases by sub-atmospheric initial 40Ar/36Ar ratios, and more generally in sub-atmospheric 38Ar/36Ar. Resulting bias can be avoided through the use of isochron ages, which do not entail the assumption of an initial value of 40Ar/36Ar as is required for plateau ages. Since step heating of glasses often yields limited variability in 40Ar:39Ar:36Ar (and therefore little spread on isochrons), another approach is to use an average value for initial 40Ar/36Ar, with concomitantly larger uncertainty than is associated with atmospheric 40Ar/36Ar, when calculating a plateau age. The 38Ar/36Ar of an un-irradiated subset of our samples validates the inference of kinetic fractionation, and potentially provides a basis for determining initial 40Ar/36Ar in samples that fail to yield isochrons, but only in samples lacking magmatic excess 40Ar. These approaches allow us to reliably apply the 40Ar/39Ar method to volcanic glasses, which has resulted in maximum ages for archaeological sites that are not amenable to traditional geochronological methods. 40Ar/39Ar geochronology can also provide information on the geological provenance of the raw material used for tool making, especially when combined with geochemical data.  相似文献   

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

18.
Equations describing trace element and isotopic evolution in a magma chamber affected simultaneously by fractional crystallization and wallrock assimilation are presented for a model where the mass assimilation rate(?a) is an arbitrary fraction(r) of the fractional crystallization rate(?c). The equations also apply to recharge of a crystallizing magma. Relatively simple analytical expressions are obtained for both radiogenic isotope variations (Nd, Sr, Pb) and stable isotopes (O, H) including the effects of mass-dependent fractionation. Forr = 1 a modified zone refining equation is obtained for trace element concentrations, but forr < 1 behavior is a combination of zone refining and fractional crystallization. Asr → ∞, simple binary mixing is approached. The isotopic and trace element “mixing” trends generated can be much different from binary mixing, especially forr < 1. The model provides the basis for a more general approach to the problem of wallrock assimilation, and shows that binary mixing models are insufficient to rule out crustal assimilation as a cause of some of the isotopic variations observed in igneous rocks, including cases where clustering of isotopic values occurs partway between presumed endmember values. The coupled assimilation-fractional crystallization model provides an explanation for certain trace element and isotopic properties of continental margin orogenic magmas (e.g. Sr concentration versus87Sr/86Sr) which had previously been interpreted as evidence against assimilation. So-called “pseudoisochrons” can be understood as artifacts of contamination using this model. A significant correlation exists between country rock age and low143Nd/144Nd ratios in continental igneous rocks, clearly suggestive that crustal contamination is generally important.  相似文献   

19.
Noble gas elemental and isotopic abundances were measured in seven deep-sea water samples from five different sampling sites in the Nankai Trough, the Japan Trench and the Kuril Trench. The samples were obtained by the manned submersible “Nautile”. Most of the sampling sites are associated with clam colonies and/or fluid venting. Excesses both in3He/4He ratio and He concentration are observed in a seawater sample collected a few kilometers off the clam colonies which were found at a depth of 3830 m at the mouth of the Tenryu Canyon. Concentrations of noble gases (Ne, Ar, Kr and Xe) in this sample show progressive depletion from Ne to Xe relative to those in 1°C air-saturated seawater, which can be attributed to mixing of hot water ( 15°C) with cold ambient water ( 1°C). Isotopic compositions of Ne, Ar, Kr and Xe in this sample are atmospheric. These observations may reflect venting of hot pore water around the Tenryu Canyon. All the other samples show a significant excess in concentration of all noble gases relative to 1°C air-saturated seawater and the isotopic compositions are atmospheric. This excess of noble gas concentrations may appear to be air contamination in the samples. However, results of hydrocarbon analyses of the Kaiko samples imply that such large amount of air contamination is improbable. Decomposition of gas hydrate in deep-sea sediments is a more likely explanation for the observed excess of noble gas concentration.  相似文献   

20.
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   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号