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1.
The noble gases He, Ne, Ar, Kr and Xe and also K and Ba were measured in the Apollo 11 igneous rocks 10017 and 10071, and in an ilmenite and two feldspar concentrates separated from rock 10071. Whole rock K/Ar ages of rocks 10017 and 10071 are (2350 ± 60) × 106 yr and (2880 ± 60) × 106 yr, respectively. The two feldspar concentrates of rock 10071 have distinctly higher ages: (3260 ± 60) × 106 yr and (3350 ± 70) × 106 yr. These ages are still 10 per cent lower than the Rb/Sr age obtained by Papanastassiouet al. (1970) and some Ar40 diffusion loss must have occurred even in the relatively coarse-grained feldspar.The relative abundance patterns of spallation Ne, Ar, Kr and Xe are in agreement with the ratios predicted from meteoritic production rates. However, diffusion loss of spallation He3 is evident in the whole rock samples, and even more in the feldspar concentrates. The ilmenite shows little or no diffusion loss. The isotopic composition of spallation Kr and Xe is similar to the one observed in meteorites. Small, systematic differences in the spallation Kr spectra of rocks 10017 and 10071 are due to variations in the irradiation hardness (shielding). The Kr spallation spectra in the mineral concentrates are different from the whole rock spectra and also show individual variations, reflecting the differences in target element composition. The relative abundance of cosmic ray produced Xe131 differs by nearly 50 per cent in the two rocks. The other Xe isotopes show no variations of similar magnitude. The origin of the Xe131 yield variability is discussed.Kr81 was measured in all the samples investigated. The Kr81/Kr exposure ages of rocks 10017 and 10071 are (480 ± 25) × 106 yr and (350 ± 15) × 106 yr, respectively. Exposure ages derived from spallation Ne21, Ar38, Kr83 and Xe126 are essentially in agreement with the Kr81/Kr ages. The age of rock 10071 might be somewhat low because of a possible recent exposure of our sample to solar flare particles.  相似文献   

2.
He, Ne and Ar isotopes have been measured in six, and 26Al in two diogenites. Cosmic-ray exposure ages corrected for shielding effects using 22Ne/21Ne ratios are generally concordant. Five diogenites have a group age of 14 Myr and three others may have a group age of 24 Myr, implying that two collisions may have produced 8 of the 9 diogenites.  相似文献   

3.
The Sulagiri meteorite fell in India on 12 September 2008,LL6 chondrite class is the largest among all the Indian meteorites.Isotopic compositions of noble gases(He,Ne,Ar,Kr and Xe) and nitrogen in the Sulagiri meteorite and cosmic ray exposure history are discussed.Low cosmogenic(~(22)Ne/~(21)Ne)_c ratio is consistent with irradiation in a large body.Cosmogenic noble gases indicate that Sulagiri has a 4πcosmic-ray exposure(CRE) age of 27.9 ± 3.4 Ma and is a member of the peak of CRE age distribution of IX chondrites.Radiogenic ~4He and ~(40)Ar concentrations in Sulagiri yields the radiogenic ages as 2.29 and4.56 Ca,indicating the loss of He from the meteorite.Xenon and krypton are mixture of Q and spallogenic components.  相似文献   

4.
The San Juan Basin natural gas field, located in northwestern New Mexico and southwestern Colorado in the USA, is a case-type coalbed methane system. Groundwater is thought to play a key role in both biogenic methane generation and the CO2 sequestration potential of coalbed systems. We show here how noble gases can be used to construct a physical model that describes the interaction between the groundwater system and the produced gas. We collected 28 gas samples from producing wells in the artesian overpressured high production region of the basin together with 8 gas samples from the underpressured low production zone as a control. Stable isotope and major species determination clearly characterize the gas in the high production region as dominantly biogenic in origin, and the underpressured low producing region as having a significant admix of thermogenic coal gas. 3He/4He ratios increase from 0.0836Ra at the basin margin to 0.318Ra towards the center, indicating a clear but small mantle He signature in all gases. Coherent fractionation of water-derived 20Ne/36Ar and crustal 4He/40Ar* are explained by a simple Rayleigh fractionation model of open system groundwater degassing. Low 20Ne concentrations compared to the model predicted values are accounted for by dilution of the groundwater-associated gas by desorbed coalbed methane. This Rayleigh fractionation and dilution model together with the gas production history allows us to quantify the amount of water involved in gas production at each well. The quantified water volumes in both underpressured and overpressured zones range from 1.7 × 103 m3 to 4.2 × 105 m3, with no clear distinction between over- and underpressured production zones. These results conclusively show that the volume of groundwater seen by coal does not play a role in determining the volume of methane produced by secondary biodegradation of these coalbeds. There is no requirement of continuous groundwater flow for renewing the microbes or nutrient components. We furthermore observe strong mass related isotopic fractionation of 20Ne/22Ne and 38Ar/36Ar isotopic ratios. This can be explained by a noble gas concentration gradient in the groundwater during gas production, which causes diffusive partial re-equilibration of the noble gas isotopes. It is important for the study of other systems in which extensive groundwater degassing may have occurred to recognize that severe isotopic fractionation of air-derived noble gases can occur when such concentration gradients are established during gas production. Excess air-derived Xe and Kr in our samples are shown to be related to the diluting coalbed methane and can only be accounted for if Xe and Kr are preferentially and volumetrically trapped within the coal matrix and released during biodegradation to form CH4.  相似文献   

5.
We present the elemental and isotopic composition of noble gases in the bulk solar wind collected by the NASA Genesis sample return mission. He, Ne, and Ar were analyzed in diamond-like carbon on a silicon substrate (DOS) and 84,86Kr and 129,132Xe in silicon targets by UV laser ablation noble gas mass spectrometry. Solar wind noble gases are quantitatively retained in DOS and with exception of He also in Si as shown by a stepwise heating experiment on a flown DOS target and analyses on other bulk solar wind collector materials. Solar wind data presented here are absolutely calibrated and the error of the standard gas composition is included in stated uncertainties. The isotopic composition of the light noble gases in the bulk solar wind is as follows: 3He/4He: (4.64 ± 0.09) × 10−4, 20Ne/22Ne: 13.78 ± 0.03, 21Ne/22Ne: 0.0329 ± 0.0001, 36Ar/38Ar 5.47 ± 0.01. The elemental composition is: 4He/20Ne: 656 ± 5, and 20Ne/36Ar 42.1 ± 0.3. Genesis provided the first Kr and Xe data on the contemporary bulk solar wind. The preliminary isotope and elemental composition is: 86Kr/84Kr: 0.302 ± 0.003, 129Xe/132Xe: 1.05 ± 0.02, 36Ar/84Kr 2390 ± 150, and 84Kr/132Xe 9.5 ± 1.0. The 3He/4He and the 4He/20Ne ratios in the Genesis DOS target are the highest solar wind values measured in exposed natural and artificial targets. The isotopic composition of the other noble gases and the Kr/Xe ratio obtained in this work agree with data from lunar samples containing “young” (∼100 Ma) solar wind, indicating that solar wind composition has not changed within at least the last 100 Ma. Genesis could provide in many cases more precise data on solar wind composition than any previous experiment. Because of the controlled exposure conditions, Genesis data are also less prone to unrecognized systematic errors than, e.g., lunar sample analyses. The solar wind is the most authentic sample of the solar composition of noble gases, however, the derivation of solar noble gas abundances and isotopic composition using solar wind data requires a better understanding of fractionation processes acting upon solar wind formation.  相似文献   

6.
Solubilities of noble gases in magnetite were determined by growing magnetite in a noble-gas atmosphere between 450 and 700°K. Henry's law is obeyed at pressures up to 10?2 atm for He, Ne, Ar and up to 10?5 atm for Kr, Xe, with the following distribution coefficients at 500° (cc STP g?1 atm?5): He 0.042, Ne 0.016, Ar 3.6, Kr 1.3, Xe 0.88, some 102–105 times higher than previous determinations on silicate and fluoride melts. Apparent heats of solution in kcal/mole are: He ?2.42 ±0.12, Ne ?2.20 ±0.10, Ar ?15.25 ±0.25, Kr ?13.0 ±0.3, Xe ?12-5 ± 0.5. These values, too, stand in sharp contrast with earlier determinations on melts which were small and positive, but are comparable to the values for clathrates. Presumably the gases are held in anion vacancies.Extrapolation of the magnetite data to the formation temperature of C1 chondrites, 360°K, shows that the Arp36 content of Orgueil magnetite could be acquired by equilibrium solubility at a total nebular pressure of 4 × 10?6 atm. In the absence of data for silicates (the principal host phase of planetary gas), an attempt is made to estimate the solubilities required to account for planetary gases in meteorites. These values do not appear grossly unreasonable in the light of the magnetite data, when structural differences between the two minerals are taken into account. It seems that equilibrium solubility may be able to account for four features of planetary gas: elemental ratios, amounts, correlations with other volatiles and retentive siting. It cannot account for the isotopic fractionation of planetary gas, however.  相似文献   

7.
The effectiveness of carbon capture and geologic storage depends on many factors, including and especially the permeability of the reservoir’s caprock. While caprock integrity is generally assumed if petroleum has been preserved, it is poorly constrained in reservoirs containing only saline waters, and CO2 leakage poses a potential risk to shallow aquifers. Naturally-occurring He accumulates in pore waters over time with the concentration being strongly dependent on the long term flux of fluid through the caprock. Furthermore, a small fraction of pore-water He diffuses into quartz and this may be used as a proxy for He concentrations in pore water, where dissolved gas samples are difficult to obtain, such as in deep sedimentary basins. In this paper He contained in quartz grains is measured and compared to previously measured pore water concentrations. Quartz was purified from core samples from the San Juan Basin, New Mexico and the Great Artesian Basin, South Australia. Quartz separates were heated at 290 °C to release He from the quartz. The quartz from the San Juan Basin and high purity quartz from the Spruce Pine Intrusion, North Carolina was repeatedly impregnated at varying pressures using pure He, heated and analyzed to build He sorption isotherms. The isotherms appear linear but vary between samples, possibly due to fluid inclusions within the quartz grains as high purity quartz samples partition only 1.5% of He that partitions into San Juan Basin samples. Concentrations of He in the pore water were calculated using the He-accessible volume of the quartz and the air–water He solubility. The mean San Juan Basin He pore water concentration was 2 × 10–5 cc STP He/g water, ∼400 times greater than atmospheric solubility. Great Artesian Basin samples contain a mean He concentration of 3 × 10–6 cc STP He/g water or 65 times greater than atmospheric solubility. However, pore water He concentrations in both the San Juan and Great Artesian Basins differ by up to an order of magnitude compared to samples collected with an alternate method. The reason for the offset is attributable to either partial saturation of the pore volume or a lack of He equilibrium between quartz and pore water. Coating of clay or other mineral phases on quartz grains, which tends to reduce the effective diffusion coefficient, may cause the latter. This technique of assessing permeability is promising due to the abundance of existing core samples from numerous basins where carbon sequestration may ultimately occur.  相似文献   

8.
Noble gas isotopes of HIMU and EM ocean island basalts from the Cook-Austral and Society Islands were investigated to constrain their origins. Separated olivine and clinopyroxene (cpx) phenocrysts were used for noble gas analyses. Since samples are relatively old, obtained from the oceanic area and showing chemical zoning in cpx phenocrysts, several tests on sample preparation and gas extraction methods were performed. First, by comparing heating and crushing methods, it has been confirmed that the crushing method is suitable to obtain inherent magmatic noble gases without radiogenic and cosmogenic components which were yielded after eruption, especially for He and Ne analyses. Second, noble gas compositions in the core and the rim of cpx phenocrysts were measured to evaluate the zoning effect on noble gases. The result has been that noble gas concentrations and He and Ne isotope ratios are different between them. The enrichment of noble gases in the rim compared to the core is probably due to fractional crystallization. Difference of He and Ne isotope ratios is explained by cosmogenic effect, and isotope ratios of the trapped component seem to be similar between the rim and the core. Third, leaching test reveals no systematic differences in noble gas compositions between leached and unleached samples.3He/4He ratios of HIMU samples in the Cook-Austral Islands are uniform irrespective of phenocryst type (olivine and cpx) and age of samples (10–18 Ma), and lower (average 6.8 RA) than those of the Pacific MORB. On the other hand, 3He/4He of EM samples in the Cook-Austral Islands are similar to MORB values. EM samples in the Society Islands show rather higher 3He/4He than MORB. Ne, Kr and Xe isotope ratios are almost atmospheric within analytical uncertainties. 40Ar/36Ar are not so high as those of MORB. Anomalous noble gas abundance pattern such as He and Ne depletion and Kr and Xe enrichment relative to atmospheric abundances was observed. Furthermore, Ne/Ar and Kr/Ar show correlation with some trace elemental ratios like La/Yb.Lower 3He/4He of HIMU than MORB values requires relatively high time-integrated (U + Th)/3He for the HIMU source, which suggests that the HIMU source was produced from recycled materials which had been once located near the Earth’s surface. Moreover, extreme noble gas abundance pattern and strong correlation of Ne/Ar and Kr/Ar with La/Yb indicate that the HIMU endmember is highly depleted in light noble gases and enriched in heavy noble gases. Such feature is not common to mantle materials and is rather similar to the noble gas abundance patterns of the old oceanic crust and sediment, which supports the model that the HIMU source originates from subducted oceanic crust and/or sediment.If the HIMU source corresponds to the oceanic crust which subducted at 1–2 Ga as suggested by Pb isotope studies, however, the characteristic 3He/4He of HIMU (6.8 RA) would be too high because radiogenic 4He produced by U and Th decay should dramatically decrease 3He/4He. To overcome this problem, the He open system model is introduced which includes the effects of 4He production and diffusion between the HIMU source material and the surrounding mantle. This model favors that the HIMU source resides in the upper mantle, rather than in the lower mantle. Furthermore, this model predicts the thickness of the HIMU source to be in the order of 1 km.In contrast to low and uniform 3He/4He character of HIMU, 3He/4He of EM are rather variable. Entrainment of upper mantle material and/or a less-degassed component are required to explain the observed 3He/4He of EM in the Polynesian area. Participation of the less-degassed component would be related to the “superplume” below the Polynesian region.  相似文献   

9.
Noble gases, C and S are lost from Allende samples heated for 1 week at temperatures of 400–1000°C in a low pressure environment. In the extreme, losses of 3He and 4He are ~ 100 × while for C. S and Ne, Ar and Kr isotopes and 132Xe. these are ≤10 ×. Except for He, these losses are less severe than those of Bi or Tl from samples heated in the same runs. Significant He. Ne and Ar isotopic fractionation during heating indicates preferential outgassing of specific reservoirs. Apparent activation energies for all species generally indicate loss controlled by a diffusive process. Next to He, 40Ar is the most labile of those species considered here but still less so than Bi or Tl. L-group (but not H- or LL-group) chondrites may have lost mobile elements like Tl while being outgassed after late impact-associated heating. A less likely alternative possibility involving a collateral relation between condensation conditions and depth in a parent object may also explain the L-group trend.  相似文献   

10.
The interpretation of noble gas concentrations in groundwater with respect to recharge temperature and fractionated excess gas leads to different results on paleo-climatic conditions and on residence times depending on the choice of the gas partitioning model. Two fractionation models for the gas excess are in use, one assuming partial re-equilibration of groundwater supersaturated by excess air (PR-model, Stute et al., 1995), the other assuming closed-system equilibration of groundwater with entrapped air (CE-model, Aeschbach-Hertig et al., 2000). In the example of the Continental Terminal aquifers in Niger, PR- and CE- model are both consistent with the data on elemental noble gas concentrations (Ne, Ar, Kr, and Xe). Only by including the isotope ratio 20Ne/22Ne it can be demonstrated that the PR-model has to be rejected and the CE-model should be applied to the data. In dating applications 3He of atmospheric origin (3Heatm) required to calculate 3H-3He water ages is commonly estimated from the Ne excess presuming that gas excess is unfractionated air (UA-model). Including in addition to the Ne concentration the 20Ne/22Ne ratio and the concentration of Ar enables a rigorous distinction between PR-, CE- and UA-model and a reliable determination of 3Heatm and of 3H-3He water ages.  相似文献   

11.
Helium, neon, argon, krypton and xenon data are presented from stepwise heating of samples of the mineral whitlockite from the chondritic meteorite St. Severin. The xenon is shown to be a uniform mixture derived from 244Pu fission and rare-earth element spallation. The krypton similarly contains spallation products and 86Kr from 244Pu fission. Plutonium-244 fission yields of 86Kr/129Xe/131Xe/132Xe/134Xe/136Xe = 1.9 ± 0.5/4.8 ± 5.5/24.6 ± 2.0/88.5 ±3.0/93.9 ± 0.8/  100 are obtained. The helium, neon and argon are dominated by spallation and radiogenic 4He and 40Ar. A pile neutron irradiation experiment does not yield a unique Pu/U ratio for this mineral but yields ratios varying from 0.045 down to 0.017. Both the high concentration of 244Pu fission xenon and the high ratio of Pu/U previously reported by Wasserburget al. (J. Oeophys. Res. 74, 4221–4232, 1969) are thus confirmed.  相似文献   

12.
Five chondrites with short cosmic ray exposure ages (< 3Myr) have been analyzed for 53Mn (t1.2 = 3.7Myr), 26Al(t1.2 = 0.72Myr) and the stable isotopes of He, Ar, and in particular, Ne. In addition, rare gases were determined for five other short-lived chondrites from the same aliquots which had previously been used for 26Al and 53Mn determinations by the Cologne Laboratory. Improved curves of growth were constructed for 26Al and 53Mn to deduce the respective saturation values 26Al0 and 53Mn0 and to obtain 21Ne production rates (21P).26Al and 53Mn saturation values deduced from short-lived chondrites alone agree within 20%, with those deduced from all chondrites. Values of 21p based on 53Mn and 26Al are 0.30 ± 0.03 and 0.46 ± 0.05, respectively, in H chondrites. Possible causes for the difference include half-life errors, data selection and a recent (?2.5Myr) increase in the cosmic ray intensity.  相似文献   

13.
The rates of production of21Ne and22Ne in spallation reactions, both due to solar as well as galactic cosmic rays, in some major meteoritic minerals, e.g. olivines, feldspars and pyroxenes, are calculated using their energy spectra and excitation functions. The production profiles of21Ne and22Ne due to galactic cosmic rays, and the22Ne/21Ne ratio depend upon the size of the meteoroid. The22Ne/21Ne ratio is very sensitive to the abundance of sodium and consequently its depth profile is distinctly different in feldspars, the ratio increasing with depth rather than decreasing as in pyroxenes and olivines. In the near-surface regions, up to a depth of 2cm, production due to solar flare protons dominates, giving rise to a steep gradient in isotopic production as well as in the22Ne/21Ne ratio. Composite production profiles are given and compared with measurements in some meteorites.  相似文献   

14.
We present the results of physical properties, petrography, bulk chemistry, mineral compositions, phase relations modelling and Noble gases study of the meteorite El Pozo. The petrography and mineral compositions indicate that the meteorite is an L5 chondrite with a low shock stage of S2-S3. Heterogenous weathering was preferentially along shock structures. Thermobarometric calculations indicate thermal equilibrium conditions between 768?°C and 925?°C at ～4 to 6?kb, which are substantially consistent with the petrological metamorphism type 5. A pseudosection phase diagram is relatively consistent with the mineral assemblage observed and PT conditions calculated. Temperature vs. fO2 diagram shows that plagioclase compositional stability is very sensitive to Tschermack substitution in orthopyroxene, clinopyroxene and XAn plagioclase during the high temperature metamorphic process. Based on noble gases He, Ne, Ar and K contents a cosmogenic exposure age CRE of 1.9?Myr was calculated. The 21Ne would be totally cosmogenic, with no primordial Ne. The 21Ne/22Ne value (0.97) is higher than solar value. According to the cosmogenic Ne content, we argue that El Pozo chondrite originally had a pre-atmospheric mass of 9–10?kg, which would have been produced by a later collision after the recognized collision of the L-chondrite parent body ～470?Ma ago.  相似文献   

15.
《Applied Geochemistry》1998,13(4):441-449
Noble gas elemental and isotopic compositions have been measured as well as the abundance of C and its isotopic ratios in 11 glasses from submarine pillow basalts collected from the Mariana Trough. The 3He/4He ratios of 8.22 and 8.51 Ratm of samples dredged from the central Mariana Trough (∼18°N) agree well with that of the Mid-Ocean Ridge Basalt (MORB) glasses (8.4±0.3 Ratm), whereas a mean ratio of 8.06±0.35 Ratm in samples from the northern Mariana Trough (∼20°N) is slightly lower than those of MORB. One sample shows apparent excess of 20Ne and 21Ne relative to atmospheric Ne, suggesting incorporation of solar-type Ne in the magma source. There is a positive correlation between 3He/4He and 40Ar/36Ar ratios, which may be explained by mixing between MORB-type and atmospheric noble gases. Excess 129Xe is observed in the sample which also shows 20Ne and 21Ne excesses. Observed δ13C values of ∼20°N samples vary from −3.76‰ to −2.80‰, and appear higher than those of MORB, and the corresponding CO2/3He ratios are higher than those of MARA samples at ∼18°N, suggesting C contribution from the subducted slab.  相似文献   

16.
《Applied Geochemistry》2000,15(8):1137-1167
4He concentrations in excess of the solubility equilibrium with the atmosphere by up to two to three orders of magnitude are observed in the Carrizo Aquifer in Texas, the Ojo Alamo and Nacimiento aquifers in the San Juan Basin, New Mexico, and the Auob Sandstone Aquifer in Namibia. A simple 4He accumulation model is applied to explain these excess 4He concentrations in terms of both in situ production and a crustal flux across the bottom layer of the aquifer. Results from the model simulations suggest variability in the 4He fluxes, ranging from 6×10−6 cm3 STP cm−2 yr−1 for the Auob Sandstone Aquifer to 3.6×10−7 cm3 STP cm−2 yr−1 for the Carrizo aquifer. For the Ojo Alamo and Nacimiento aquifers an intermediate value of 3×10−6 cm3 STP cm−2 yr−1 was estimated. The contribution of in-situ produced 4He to the measured concentrations was also estimated. This contribution is negligible for the Auob Sandstone Aquifer as compared with both the concentrations measured at the top and bottom of the aquifer for most of the pathway. In the Carrizo aquifer, in-situ produced 4He contributes 27.5% and 15.4%, to the total 4He observed at the top and bottom of the aquifer, respectively. For both aquifers of the San Juan Basin in-situ production almost entirely dominates the 4He concentrations at the top of the aquifer for most of the pathway. In contrast, the internal production is negligible as compared with the measured concentrations at the bottom of these aquifers, reaching, at most, 1.1%. The model simulations require an exponential decrease in the horizontal velocity of the water with increasing recharge distance to reproduce the distribution of 4He in these aquifers. For the Auob Sandstone Aquifer the highest range in the velocity values is obtained (25 to 0.4 m yr−1). The simulations for the Carrizo aquifer and both aquifers located in the San Juan Basin require velocities varying from 4 to 0.1 m yr−1, and from 2 to 0.3 m yr−1, respectively. For each aquifer, average permeability values were also estimated. They are generally in agreement with results obtained from pumping tests, hydrodynamic modeling and previous 14C measurements. On the basis of the results obtained by calibrating the model with the measured 4He concentrations, the mean water residence times were estimated. They agree reasonably well with 14C ages. When applied as chronologies for noble gas temperatures in the same aquifers, the calculated 4He ages allow the identification of three different climate periods similar to those previously identified using 14C ages: (1) the Holocene period (0–10 Ka BP), (2) the Last Glacial Maximum (≈18 Ka BP), and (3) the preceeding period (30–150 Ka BP).  相似文献   

17.
Mineral-melt partition coefficients of all noble gases (min/meltDi) have been obtained for olivine (ol) and clinopyroxene (cpx) by UV laser ablation (213 nm) of individual crystals grown from melts at 0.1 GPa mixed noble gas pressure. Experimental techniques were developed to grow crystals virtually free of melt and fluid inclusions since both have been found to cause profound problems in previous work. This is a particularly important issue for the analysis of noble gases in crystals that have very low partition coefficients relative to coexisting melt and fluid phases. The preferred partitioning values obtained for the ol-melt system for He, Ne, Ar, Kr, and Xe are 0.00017(13), 0.00007(7), 0.0011(6), 0.00026(16), and , respectively. The respective cpx-melt partition coefficients are 0.0002(2), 0.00041(35), 0.0011(7), 0.0002(2), and . The data confirm the incompatible behaviour of noble gases for both olivine and clinopyroxene but unlike other trace elements these values show little variation for a wide range of atomic radius. The lack of dependence of partitioning on atomic radius is, however, consistent with the partitioning behaviour of other trace elements which have been found to exhibit progressively lower dependence of min/meltDi on radius as the charge decreases. As all noble gases appear to exhibit similar min/meltDi values we deduce that noble gases are not significantly fractionated from each other by olivine and clinopyroxene during melting and fractional crystallisation. Although incompatible, the partitioning values for noble gases also suggest that significant amounts of primordial noble gases may well have been retained in the mantle despite intensive melting processes. The implication of our data is that high primordial/radiogenic noble gas ratios (3He/4He, 22Ne/21Ne, and 36Ar/40Ar) characteristic of plume basalt sources can be achieved by recycling a previously melted (depleted) mantle source rather than reflecting an isolated, non-degassed primordial mantle region.  相似文献   

18.
Recent results on cosmic ray interactions in lunar samples and meteorites resulting in production of stable and radionuclides, particle tracks and thermoluminescence are reviewed. A critical examination of26A1 depth profiles in lunar rocks and soil cores, together with particle track data, enables us to determine the long term average fluxes of energetic solar protons (>10 MeV) which can be represented by (J s,R o)=(125, 125). The lunar rock data indicate that this flux has remained constant for 5×105 to 2×106 years. Production rates of stable and radionuclides produced by galactic cosmic rays is given as a function of size and depth of the meteoroid. Radionuclide (53Mn,28Al) depth profiles in meteorite cores, whose preatmospheric depths are deduced from track density profiles are used to develop a general procedure for calculating isotope production rates as a function of meteoroid size. Based on the track density and22Ne/21Ne production rates, a criterion is developed to identify meteorites with multiple exposure history.22Ne/21Ne ratio <1·06 is usually indicative of deep shielded exposure. An examination of the available data suggests that the frequency of meteorites with multiple exposure history is high, at least 15% for LL, 27% for L and 31% for H chondrites. The epi-thermal and the thermal neutron density profiles in different meteorites are deduced from60Co and track density data in Dhajala, Kirin and Allende chondrites. The data show that the production profile depends sensitively on the size and the chemical composition of the meteoroid. Cosmic ray-induced thermoluminescence in meteorites of known preatmospheric sizes has been measured which indicates that its production profile is nearly flat and insensitive to the size of the meteoroid. Some new possibilities in studying cosmic ray implanted radionuclides in meteorites and lunar samples using resonance ionisation spectroscopy are discussed.  相似文献   

19.
对华南前寒武系变质岩浆杂岩稀有气体He、Ne、Ar和Xe的系统研究表明:扬子克拉通基底为含高3He的下地壳"原始岩石层",(3He/4He)×10-6比值为2.8～4.6;而华夏板块基底变质岩浆杂岩则是在缺乏3He、低(3He/4He)×10-8比值(3.15～17.7)的构造环境下形成的大陆中-上地壳变质岩浆杂岩层,反映出两者基底性质迥然不同。华南中-新生代爆破岩筒He同位素组成相反,相对稳定的扬子克拉通(3He/4He)×10-8比值仅0.18～4.22,而郯庐-四会-吴川断裂以东,中-新生代活动地块(太平洋构造域)(3He/4He)×10-8比值高达3.7～20.5。He同位素表明郯庐-四会-吴川断裂带为切割深至地幔的边界深大断裂,是扬子克拉通与华夏板块间的边界且控制了燕山期火山-侵入岩浆向西扩展。Ar同位素组成表明华南大陆中-新生代地幔形成接近"均一"的地幔组份。136Xe/130Xe-129Xe/130Xe相关组份表明它们具有地幔柱岩石同位素组成特征。  相似文献   

20.
He, Ne, Ar, Kr and Xe concentrations and isotopic abundances were measured in three bulk grain size fractions prepared from sample L-16-19, No. 120 (C level, 20–22 cm depth) returned by the Luna 16 mission. The expected anticorrelation between the concentrations of trapped solar wind noble gases and grain size is observed. Elemental abundances of solar wind trapped noble gases are similar to those previously found in corresponding grain size fractions of the Apollo 11 and 12 fines. The trapped ratio 4He20Ne varies in the soils from different lunar maria due to diffusion losses. A rough correlation of 4He20Ne with the proportion of ilmenite in these samples is apparent. The elemental and isotopic ratios of the surface correlated noble gases in Luna 16 resemble those previously found in Apollo fines. Based on 21Ne, 78Kr and 126Xe a cosmic ray exposure age of 360 my was determined. This age is similar to those obtained for the soils from other lunar maria.  相似文献   

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