Noble gas study of HIMU and EM ocean island basalts in the Polynesian region

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 R_A) 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 R_A) 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.     

Noble gases,nitrogen and cosmic ray exposure age of the Sulagiri chondrite

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.     

金川Cu-Ni-PGE硫化物矿床成矿过程稀有气体同位素组成示踪

稀有气体同位素在示踪成矿作用流体来源方面具有独特优势。本文应用熔融质谱法测定了金川Cu-Ni-PGE硫化物矿床23个硅酸盐矿物和金属硫化物单矿物的He、Ne和Ar丰度和同位素组成。结果表明,硅酸盐矿物的3He/4He比值(0.239Ra)略低于硫化物(平均0.456Ra),且从橄榄石(平均0.291Ra)、斜方辉石(0.215Ra)到单斜辉石(0.174Ra)逐渐降低,20Ne/22Ne-21Ne/22Ne分布于MORB与大陆地壳演化线之间,扣除放射性成因4He*和40Ar*后橄榄石和辉石中3He/4He和40Ar/36Ar接近岩石圈地幔组成。He、Ne和Ar同位素组成示踪表明成矿岩浆中存在岩石圈地幔(SCLM)、地壳(CC)和大气饱和流体(ASW)三种端元成分,硫化物熔体的分离发生在岩浆结晶分异的早期。岩石圈地幔部分熔融形成的成矿初始岩浆经历了两阶段的演化。在深部岩浆房高温成矿岩浆同化围岩引入地壳混染组分,促使硫饱和及硫化物熔体的熔离,同时形成具有壳幔混合特征的混合岩浆组分(MC),上升至上部岩浆房后混入较高比例的大气饱和流体,进一步促使硫饱和及浸染状硫化物就地熔离堆积。     

He,Ne and Ar in chondritic NiFe as irradiation hardness sensors

Noble gas analyses of the Ni-Fe of 9 L, 5 H and 2 LL chondrites quantitatively support previous suggestions of radiogenic ⁴He recoil and ³He deficits. Furthermore, noble gases in the Ni-Fe show evidence for in situ produced radiogenic ⁴He and in some cases for recoil loss of ³⁸Ar and gain of ²¹Ne.The ratio of spallogenic ²¹Ne and ³⁸Ar in the metal phase is found to correlate strongly with ³He/²¹Ne and ²²Ne/²¹Ne in bulk samples of these chondrites. This is proof of the dependence of these ratios on the irradiation hardness experienced by the meteoroid in space. ‘Hardness indices’ n = 1.9–2.2 are found, indicating that on the average the stone meteoroids from which the samples came were smaller in mass than iron meteoroids. The spallogenic ²¹Ne/³⁸Ar ratio in metallic Ni-Fe can be used with the semi-empirical production model deduced from the Grant iron meteorite to calibrate spallogenic ³He/²¹Ne and ⁴Ne/²¹Ne in bulk samples of L, LL and H chondrites for meteoroid size and sample location allowing the estimation of minimal meteoroid masses. ³He and ²¹Ne production rates calculated from previously determined ³⁶Ar/³⁸Ar exposure ages for four L chondrites indicate that they are probably not single-valued functions of the ³He/²¹Ne ratio. The ratio of ³He in bulk samples to ³⁸Ar in metal samples of the same meteorite is constant (= 20 ± 3) whereas the ratio of ²¹Ne in the bulk to ³⁸Ar in the metal varies by as much as a factor of two in correlation with ³He/²¹Ne.     

Heterogeneous lithospheric mantle metasomatism in the eastern North China Craton: He–Ar isotopes in peridotite xenoliths from Cenozoic basalts

The abundances and isotopic compositions of Helium and Argon have been analyzed in a suite of fresh spinel peridotite xenoliths in Cenozoic basalts from the eastern North China Craton (NCC) by step-wise heating experiments, to investigate the nature of noble gas reservoirs in the subcontinental lithospheric mantle beneath this region. The xenoliths include one harzburgite collected from Hebi in the interior of the NCC, two lherzolites from Hannuoba at the northern margin of the craton, and three lherzolites from Shanwang and Nushan on the eastern margin. ³He/⁴He ratios in most of the xenoliths are similar to those of mid-ocean ridge basalts (MORB) or slightly lower (2–10.5 Ra, where Ra is the ³He/⁴He ratio of the atmosphere), suggesting mixing of MORB-like and radiogenic components. One olivine separate from Nushan has a helium value of 25.3 Ra, probably suggesting cosmogenic ³He addition. The ⁴⁰Ar/³⁶Ar ratios vary from atmospheric value (296) to 1625, significantly lower than the MORB value. Available data of the peridotite xenoliths indicate the He and Ar isotopic systematics of the mantle reservoirs beneath the NCC can be interpreted as mixtures of at least three end-members including MORB-like, radiogenic and atmospheric components. We suggest that the MORB-like noble gases were derived from the underlying asthenosphere during mantle upwelling, whereas the radiogenic and recycled components probably were incorporated into the lithospheric mantle during circum-craton subduction of oceanic crust. Available data suggest that the MORB-like fluids are better preserved in the interior of the NCC, whereas the radiogenic ones are more prevalent at the margins. The Paleo-Asian ocean subduction system probably was responsible for the enriched and recycled noble gas signatures on the northern margin of the craton, while the Pacific subduction system could account for the observed He–Ar isotopic signatures beneath the eastern part. Therefore, integration of helium and argon isotopes reflects heterogeneous metasomatism in the lithospheric mantle and demonstrates the critical importance of lithospheric mantle modification related to both circum-craton subduction of oceanic crust and asthenospheric upwelling beneath the eastern NCC.     

Noble gas evidence for two fluids in the Baca (Valles Caldera) geothermal reservoir

Noble gas elemental and isotopic abundances were measured in steam from four wells in the Baca geothermal reservoir located in the Valles Caldera, New Mexico. The ${}^{40}\text{Ar}{}^{36}\text{Ar}$ ratio and noble gas elemental abundances relative to ³⁶Ar are all strongly correlated with 1/³⁶Ar, the inverse of the argon content. Ratios of (α,n)-produced ²¹Ne1 and radiogenic ⁴⁰Ar1 to total ⁴He (dominantly radiogenic) are nearly constant at 2.1 × 10?8 and 0.20, respectively. The ${}^3\text{He}{}^4\text{He}$ ratio covers a restricted range of 3.9 to 4.8 times atmospheric. The high ³He content of the gas indicates the presence of a helium component ultimately derived from the mantle. Kr and Xe isotopic compositions are close to atmospheric; excess ¹²⁹Xe1 is <0.25% of the total ¹²⁹Xe.The high degree of linear correlation among the various noble gas results strongly suggests that the Baca reservoir contains two distinct fluids that are produced in varying proportions from individual wells. The noble gases in fluid A (~2900 mg/1 C1) are air-like, but with lighter gases and isotopes preferentially enriched. The fluid A ³⁶Ar content is low, only 13% that of 10°C air-saturated water (ASW). The second fluid, B (~ 1700 mg/1 C1), is the dominant carrier of the radiogenic and mantle-derived gases. The heavier non-radiogenic gases are preferentially enriched in fluid B, and its ³⁶Ar content is very low, only 5–7% ASW. The source of the noble gases in fluid A is tentatively ascribed to leaching of the relatively young (<1.4 m.y.) volcanic Bandelier Tuff. The radiogenic gases and mantle-derived helium in fluid B suggest a deeper source, possibly including gases escaping from a magma.     

Regional groundwater focusing of nitrogen and noble gases into the Hugoton-Panhandle giant gas field, USA

The Hugoton-Panhandle giant gas field, located across SW Kansas and the Texas and Oklahoma panhandles in the USA, is the case type example of high nitrogen concentrations in a natural gas being linked with high helium concentrations. We collected 31 samples from producing wells in a north-south traverse of the 350-km-long field. The samples reflect the previously observed north-south change in ⁴He/N₂, with values changing from 0.020 to 0.049 respectively. ³He/⁴He, ²¹Ne/²²Ne, and ⁴⁰Ar/³⁶Ar vary between 0.14-0.25 Ra, 0.0373-0.0508, and 818-1156 respectively, and are caused by quantifiable contributions from mantle, crustal, and atmosphere-derived sources. The atmosphere-derived ²⁰Ne/³⁶Ar ratios are indistinguishable from groundwater values. The crustal ⁴He/²¹Ne* and ⁴He/⁴⁰Ar* ratios show a 60% excess of ⁴He compared to predicted production ratios in the crust and are typical of noble gases released from the shallow crust. The mantle ³He/N₂ and groundwater-recharge ³⁶Ar/N₂ ratios enable us to rule out significant magmatic or atmosphere contributions to the gas field N₂, which is dominantly crustal in origin.Correlated ²⁰Ne/N₂ and ⁴He/N₂ shows mixing between two distinct crustal N₂ components. One N₂ component (N₂*) is associated with the crustal ⁴He and groundwater-derived ²⁰Ne, and the other with no resolvable noble gas contribution. Measured δ¹⁵N_N2 values vary from +2.7‰ to +9.4‰. The N₂* and non-He-associated N₂ endmembers are inferred to have δ¹⁵N_N2 = −3‰ and +13‰ and contribute from between 25-60% and 75-40% of the nitrogen respectively. The non-He-associated nitrogen is probably derived from relatively mature organic matter in the sedimentary column. The δ¹⁵N_N2* value is not compatible with a crystalline or high-grade metamorphic source and, similar to the ⁴He, is inferred to be from a shallow or low metamorphic-grade source rock. ⁴He mass balance requires a regional crustal source, its association with significant magmatic ³He pointing to a tectonically active source to the west of the Hugoton system. The volume of groundwater required to source the ²⁰Ne in the gas field demonstrates the viability of the groundwater system in providing the collection, transport, and focusing mechanism for the ⁴He and N₂*. The N₂*/²⁰Ne ratio shows that the N₂* transport must be in the aqueous phase, and that the degassing mechanism is probably contact between the regional groundwater system and the preexisting reservoir hydrocarbon gas phase.     

Rare gas isotopes and parent trace elements in ultrabasic-alkaline-carbonatite complexes, Kola Peninsula: identification of lower mantle plume component

During the Devonian magmatism (370 Ma ago) ∼20 ultrabasic-alkaline-carbonatite complexes (UACC) were formed in the Kola Peninsula (north-east of the Baltic Shield). In order to understand mantle and crust sources and processes having set these complexes, rare gases were studied in ∼300 rocks and mineral separates from 9 UACC, and concentrations of parent Li, K, U, and Th were measured in ∼70 samples. ⁴He/³He ratios in He released by fusion vary from pure radiogenic values ∼10⁸ down to 6 × 10⁴. The cosmogenic and extraterrestrial sources as well as the radiogenic production are unable to account for the extremely high abundances of ³He, up to 4 × 10⁻⁹ cc/g, indicating a mantle-derived fluid in the Kola rocks. In some samples helium extracted by crushing shows quite low ⁴He/³He = 3 × 10⁴, well below the mean ratio in mid ocean ridge basalts (MORB), (8.9 ± 1.0) × 10⁴, indicating the contribution of ³He-rich plume component. Magnetites are principal carriers of this component. Trapped ³He is extracted from these minerals at high temperatures 1100°C to 1600°C which may correspond to decrepitation or annealing primary fluid inclusions, whereas radiogenic ⁴He is manly released at a temperature range of 500°C to 1200°C, probably corresponding to activation of ⁴He sites degraded by U, Th decay.Similar ⁴He/³He ratios were observed in Oligocene flood basalts from the Ethiopian plume. According to a paleo-plate-tectonic reconstruction, 450 Ma ago the Baltica (including the Kola Peninsula) continent drifted not far from the present-day site of that plume. It appears that both magmatic provinces could relate to one and the same deep-seated mantle source.The neon isotopic compositions confirm the occurrence of a plume component since, within a conventional ²⁰Ne/²²Ne versus ²¹Ne/²²Ne diagram, the regression line for Kola samples is indistinguishable from those typical of plumes, such as Loihi (Hawaii). ²⁰Ne/²²Ne ratios (up to 12.1) correlate well with ⁴⁰Ar/³⁶Ar ones, allowing to infer a source ⁴⁰Ar/³⁶Ar ratio of about 4000 for the mantle end-member, which is 10 times lower than that of the MORB source end-member. In (³He/²²Ne)_PRIM versus (⁴He/²¹Ne)_RAD plot the Kola samples are within array established for plume and MORB samples; almost constant production ratio of (⁴He/²¹Ne)_RAD ≅ 2 × 10⁷ is translated via this array into (³He/²²Ne)_PRIM ∼ 10. The latter value approaches the solar ratio implying the non-fractionated solar-like rare gas pattern in a plume source.The Kola UACC show systematic variations in the respective contributions of in situ-produced radiogenic isotopes and mantle-derived isotopes. Since these complexes were essentially plutonic, we propose that the depth of emplacement exerted a primary control on the retention of both trapped and radiogenic species, which is consistent with geological observations. The available data allow to infer the following sequence of processes for the emplacement and evolution of Kola Devonian UACC: 1) Ascent of the plume from the lower mantle to the subcontinental lithosphere; the plume triggered mantle metasomatism not later than ∼700 to 400 Ma ago. 2) Metasomatism of the lithosphere (beneath the central part of the Kola Peninsula), including enrichment in volatile (e.g., He, Ne) and in incompatible (e.g., U, Th) elements. 3) Multistage intrusions of parental melts, their degassing, and crystallisation differentiation ∼370 Ma ago. 4) Postcrystallisation migration of fluids, including loss of radiogenic and of trapped helium. Based on model compositions of the principle terrestrial reservoirs we estimate the contributions (by mass) of the plume material, the upper mantle material, and the atmosphere (air-saturated groundwater), into the source of parent melt at ∼2%, 97.95%, and ∼0.05%, respectively.     

Helium and Argon Isotopic Composition of Cenozoic Alkali Basalts and Mantle-Derived Xenoliths from Kuandian, Liaoning Province, China

The noble gas isotopic composition and content data of 2 alkali basalts, 3 Iherzolite xenoliths and one clinopyroxene megacryst from the Kuandian region have confirmed the occurrence of a fractionation of noble gases during magmatism. Light noble gases such as He and Ne are high in mobility and appear to be incompatible as compared with heavy ones ( such as Kr and Xe). Therefore, light noble gases are abundant in volcanics, especially in the volcanics with bubbles; lherzolite xenoliths have relatively high heavy noble gases. The clinopyroxene megacryst has the lowest abundance of noble gases, probably due to its high P-T origin. Noble gas isotopic composition of the clinopyroxene megacryst reveals that the mantle source beneath the Kuandian area has an MORB-like reservoir with^3 He/^4He ratio of—10 Ra(Ra: atmospheric^3 He/^4He ratio) and^40 Ar/^36 Ar ratio of 345.6. The Iherzolite xenoliths possess moderate^3 He/^4He ratios of 2.59 -4.53 Ra, reflecting the loss of primary helium during rock deformation or metasomatism caused by enriched mantle fluids during the up-lifting. The alkali volcanics have very low^3 He/^4 He ratios(0.47—0.61 Ra),indicating a contribution of radiogenic^4 He, probably having resulted from crust contamination. Most of the samples have excess^21 Ne and^22 Ne as compared with atmospheric neon, but Kr and Xe isotopic compositions are indistinguishable from atmospheric values within uncertainties with only individual samples having excess^129Xe,^134Xeand^136 Xe.     

Noble gases in formation fluids from deep sedimentary basins: a review

Atmospheric Ne, Ar, Kr and Xe are observed in fluids occurring in deep basins. Modifications of their abundance patterns reveal modes of recharge and brine formation, phase separations during boiling, and association of natural gas with water or oil. Radiogenic ⁴He and ⁴⁰Ar serve as age indicators of entrapped fluids, effective over a significant portion of the geological time scale. Simultaneous application of δ¹³C, atmospheric noble gases and radiogenic ⁴He and ⁴⁰Ar, is recommended to identify: (a) recent bacterial natural gas formation, not accompanied by oil, and (b) natural gas formed along with oil in a mature source rock.     

Isotopic Geochemistry of Non—hydrocarbons in Natural Gases from the Sanshui Basin,Guangdong Province,China

This study is focused on geothermal heat flow and the origin of non-hydrocarbons in natural gases in terms of the isotope geochemical characteristics of Ar, He, CO₂ and N₂ in natural gases from the Sanshui Basin, Guangdong Province. China.³He/⁴He ratios are of (1.60-6.39) × 10^-6, and⁴⁰Ar/³⁶Ar ratios of 450–841. The carbon isotopic composition (δ_l3C PDB) of carbon dioxide ranges from -20‰ to -2‰. δ^l5N(air) ratios have a wider range of-57 ‰- +95 ‰. The isotope geochemical characteristics of non-hydrocarbons indicate that He, Ar and N₂ in the gas reservoirs enriched in non-hydrocarbons were derived largely from the upper mantle. Non-hydrocarbons in gaseous hydrocarbon reservoirs consist mainly of crustal radiogenic He and⁴⁰Ar and some mantle-derived He and Ar, as well as of¹³C-depleted carbon dioxide and nitrogen generated as a result of thermal decomposition of organic matter in strata. Carbon dioxide enriched in¹³C was derived largely from carbonate rocks and partially from the lower crust and upper mantle. Based on the relationship between geothermal heat flow (Q) and³He/⁴ He ratio in natural gases, the Q values for the area studied have been calculated. Similar Q values are reported from the upper mantle uplift area (77 mWm^-2) in Huabei and the Tancheng-Lujiang Rift Zone (88 mWm^-2). More than 60 percent of geothermal heat flow in the Sanshui Basin may have been derived from the upper mantle. The project is financially supported by the National Natural Science Foundation of China.     

The noble gas systematics of late-orogenic H2O-CO2 fluids, Mt Isa, Australia

The noble gases (He, Ne, Ar, Kr and Xe) are powerful geochemical tracers because they have distinctive isotopic compositions in the atmosphere, crust and mantle. This study illustrates how noble gases can be used to trace fluid origins in high-temperature metamorphic and mineralising environments; and at the same time provides new information on the composition of noble gases in deeper parts of the crust than have been sampled previously.We report data for H₂O and CO₂ fluid inclusions trapped at greenschist to amphibolite facies metamorphic conditions associated with three different styles of mineralisation and alteration in the Proterozoic Mt Isa Inlier of Australia. Sulphide fluid inclusions are dominated by crustal ⁴He. However, co-variations in fluid inclusion ²⁰Ne/²²Ne, ²¹Ne/²²Ne, ⁴⁰Ar/³⁶Ar and ¹³⁶Xe/¹³⁰Xe indicate noble gases were derived from three or more reservoirs. In most cases, the fluid inclusions elemental noble gas ratios (e.g. Ne/Xe) are close to the ranges expected in sedimentary and crystalline rocks. However, the elemental ratios have been modified in some of the samples providing evidence for independent pulses of CO_2, and interaction of CO₂ with high-salinity aqueous fluids.Compositional variation is attributed to mixing of: (i) magmatic fluids (or deeply sourced metamorphic fluids) characterised by basement-derived noble gases with ²⁰Ne/²²Ne ∼ 8.4, ²¹Ne/²²Ne ∼ 0.4, ⁴⁰Ar/³⁶Ar ∼ 40,000 and ¹³⁶Xe/¹³⁰Xe ∼ 8; (ii) basinal-metamorphic fluids with a narrow range of compositions including near-atmospheric values and (iii) noble gases derived from the meta-sedimentary host-rocks with ²⁰Ne/²²Ne ∼ 8-9.8, ²¹Ne/²²Ne < 0.1, ⁴⁰Ar/³⁶Ar < 2500 and ¹³⁶Xe/¹³⁰Xe ∼ 2.2.These data provide the strongest geochemical evidence available for the involvement of fluids from two distinct geochemical reservoirs in Mt Isa’s largest ore deposits. In addition the data show how noble gases in fluid inclusions can provide information on fluid origins, the composition of the crust’s major lithologies, fluid-rock interactions and fluid-fluid mixing or immiscibility processes.     

Helium,neon, and argon in the iron meteorites Dongling,Nantan and Ningbo

The light noble gases He, Ne and Ar have been measured in the iron meteorites Dongling, Nantan and Ningbo. Dongling and Ningbo show a deficit of cosmic-ray that produced³He of ca. 30% and 10%, respectively, which is argued to be caused by the loss of³H (tritium) from the meteoroids during the time of their exposure to the cosmic radiation. Nantan has the lowest content of noble gases as yet reported for any iron meteorite. Cosmogenic³He and³⁸Ar are only about 1/5000 of those in Dongling which has particularly interesting implications if the two meteorites belong to the same fall^[2]. In addition, Nantan contains nonspallogenic⁴He which we believe to be of radiogenic origin. This radiogenic⁴He, together with a U-content of 2.6×10⁻¹¹ g/g^[20] yields a⁴He retention age close to the cosmic-ray exposure age of Dongling. If Dongling and Nantan were part of the same meteoroid^[2], this result would indicate that He retention in the meteoroid age were 4,500 Ma, a U-content of less than 7.2×10⁻¹³ g/g is required to explain the non-cosmogenic₄He present. An upper limit to the number of transuranium or superheavy-element atoms which have decayed by α-emission in Nantan since onset of He retention is 2×10¹⁰ per gram.     

Apparent decoupling of the He and Ne isotope systematics of the Icelandic mantle: The role of He depletion, melt mixing, degassing fractionation and air interaction

We present new He-Ne data for geothermal fluids and He-Ne-Ar data for basalts from throughout the Icelandic neovolcanic zones and older parts of the Icelandic crust. Geothermal fluids, subglacial glasses, and mafic phenocrysts are characterized by a wide range in helium isotope ratios (³He/⁴He) encompassing typical MORB-like ratios through values as high as 36.8 R_A (where R_A = air ³He/⁴He). Although neon in geothermal fluids is dominated by an atmospheric component, samples from the northwest peninsula show a small excess of nucleogenic ²¹Ne, likely produced in-situ and released to circulating fluids. In contrast, geothermal fluids from the neovolcanic zones show evidence of a contribution of mantle-derived neon, as indicated by ²⁰Ne enrichments up to 3% compared to air. The neon isotope composition of subglacial glasses reveals that mantle neon is derived from both depleted MORB-mantle and a primordial, ‘solar’ mantle component. However, binary mixing between these two endmembers can account for the He-Ne isotope characteristics of the basalts only if the ³He/²²Ne ratio of the primordial mantle endmember is lower than in the MORB component. Indeed, the helium to neon elemental ratios (⁴He/²¹Ne∗ and ³He/²²Ne_s where ²¹Ne∗ = nucleogenic ²¹Ne and ²²Ne_s = ‘solar’-derived ²²Ne) of the majority of Icelandic subglacial glasses are lower than theoretical values for Earth’s mantle, as observed previously for other OIB samples. Helium may be depleted relative to neon in high-³He/⁴He ratio parental melts due to either more compatible behavior during low-degree partial melting or more extensive diffusive loss relative to the heavier noble gases. However, Icelandic glasses show higher ⁴He/⁴⁰Ar∗ (⁴⁰Ar∗ = radiogenic Ar) values for a given ⁴He/²¹Ne∗ value compared to the majority of other OIB samples: this observation is consistent with extensive open-system equilibrium degassing, likely promoted by lower confining pressures during subglacial eruptions of Icelandic lavas. Taken together, the He-Ne-Ar systematics of Icelandic subglacial glasses are imprinted with the overlapping effects of helium depletion in the high-³He/⁴He ratio parental melt, binary mixing of two distinct mantle components, degassing fractionation and interaction with atmospheric noble gases. However, it is still possible to discern differences in the noble gas characteristics of the Icelandic mantle source beneath the neovolcanic zones, with MORB-like He-Ne isotope features prevalent in the Northern Rift Zone and a sharp transition to more primitive ‘solar-like’ characteristics in central and southern Iceland.     

Crystal-melt partitioning of noble gases (helium, neon, argon, krypton, and xenon) for olivine and clinopyroxene

Mineral-melt partition coefficients of all noble gases (^min/meltD_i) 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/meltD_i on radius as the charge decreases. As all noble gases appear to exhibit similar ^min/meltD_i 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.     

新疆坡北杂岩体西端镁铁-超镁铁质岩体成因的稀有气体同位素制约

新疆坡北镁铁-超镁铁质杂岩体由一个辉长岩体以及二十多个超镁铁质侵入体组成,其中坡一超镁铁质岩体稀有气体同位素组成揭示存在地幔柱的贡献。坡北杂岩体西端的坡一、坡四、坡十和坡十四等几个超镁铁质岩体的稀有气体同位素对比分析结果表明,岩浆矿物的³He/⁴He值（0.26~2.79Ra）分布于地壳与地幔值之间,较高的²⁰Ne/²²Ne和较低的²¹Ne/²²Ne值分布于Ne质量分馏线（MFL）和L-K线之间,⁴⁰Ar/³⁶Ar=295~598。³He/⁴He与⁴⁰Ar/³⁶Ar比值揭示坡北杂岩体西端不同超镁铁质岩体形成过程中地幔（柱）、地壳和大气组分的贡献不同,岩体成因也可能不同。其中,坡一岩体具有地幔柱作用的贡献,其他三个岩体的岩石圈地幔及地壳流体组分的贡献较大。岩浆地幔源区由深部地幔柱物质叠加俯冲流体交代的岩石圈地幔物质所组成,大气与地壳物质组分可能由俯冲再循环洋壳带入到岩浆地幔源区以及围岩物质的混入。     

广西栗木锡铌钽矿田成矿物质来源的惰性气体同位素示踪

文章利用黄铁矿流体包裹体惰性气体同位素,探讨了广西栗木锡铌钽矿田成矿流体的来源.黄铁矿流体包裹体的3He/4He比值为0.14～0.97 Ra,远远低于地幔流体的比值,接近饱和大气水的比值,并与地壳流体的比值处在相同的数量级上;40 Ar/36 Ar比值为555.98～ 855.11,平均705.55,显然偏离大气氩的同位素组成;40Ar*/4He比值为0.08～0.27,平均值为0.153,接近地壳值;20Ne/22 Ne=9.671～9.748和21Ne/22 Ne=0.0306～ 0.0330,具有饱和大气水的Ne同位素比值特征.结果表明,广西栗木锡铌钽矿田老虎头、牛栏岭和金竹源3个矿床的成矿流体是大气水和地壳流体的混合流体;水溪庙矿床的成矿流体也主要是大气水和地壳流体的混合流体,但可能有少量地幔流体的加入.     

The noble gas geochemistry of natural CO2 gas reservoirs from the Colorado Plateau and Rocky Mountain provinces, USA

Identification of the source of CO₂ in natural reservoirs and development of physical models to account for the migration and interaction of this CO₂ with the groundwater is essential for developing a quantitative understanding of the long term storage potential of CO₂ in the subsurface. We present the results of 57 noble gas determinations in CO₂ rich fields (>82%) from three natural reservoirs to the east of the Colorado Plateau uplift province, USA (Bravo Dome, NM., Sheep Mountain, CO. and McCallum Dome, CO.), and from two reservoirs from within the uplift area (St. John’s Dome, AZ., and McElmo Dome, CO.). We demonstrate that all fields have CO₂/³He ratios consistent with a dominantly magmatic source. The most recent volcanics in the province date from 8 to 10 ka and are associated with the Bravo Dome field. The oldest magmatic activity dates from 42 to 70 Ma and is associated with the McElmo Dome field, located in the tectonically stable centre of the Colorado Plateau: CO₂ can be stored within the subsurface on a millennia timescale.The manner and extent of contact of the CO₂ phase with the groundwater system is a critical parameter in using these systems as natural analogues for geological storage of anthropogenic CO₂. We show that coherent fractionation of groundwater ²⁰Ne/³⁶Ar with crustal radiogenic noble gases (⁴He, ²¹Ne, ⁴⁰Ar) is explained by a two stage re-dissolution model: Stage 1: Magmatic CO₂ injection into the groundwater system strips dissolved air-derived noble gases (ASW) and accumulated crustal/radiogenic noble gas by CO₂/water phase partitioning. The CO₂ containing the groundwater stripped gases provides the first reservoir fluid charge. Subsequent charges of CO₂ provide no more ASW or crustal noble gases, and serve only to dilute the original ASW and crustal noble gas rich CO₂. Reservoir scale preservation of concentration gradients in ASW-derived noble gases thus provide CO₂ filling direction. This is seen in the Bravo Dome and St. John’s Dome fields. Stage 2: The noble gases re-dissolve into any available gas stripped groundwater. This is modeled as a Rayleigh distillation process and enables us to quantify for each sample: (1) the volume of groundwater originally ‘stripped’ on reservoir filling; and (2) the volume of groundwater involved in subsequent interaction. The original water volume that is gas stripped varies from as low as 0.0005 cm³ groundwater/cm³ gas (STP) in one Bravo Dome sample, to 2.56 cm³ groundwater/cm³ gas (STP) in a St. John’s Dome sample. Subsequent gas/groundwater equilibration varies within all fields, each showing a similar range, from zero to ∼100 cm³ water/cm³ gas (at reservoir pressure and temperature).     

辽宁宽甸新生代火山岩和地幔包体的稀有气体同位素组成及其演化意义

通过对宽甸新生代碱性玄武岩、地幔包体及辉石巨晶的稀有气体同位素组成的分析，认为不同岩性稀有气体含量的差异反映了岩浆作用过程中轻、重稀有气体的分馏特性，较轻的稀有气体(He、Ne)比较重的稀有气体(Kr、xe)具有更高的活动性和不相容性；该地区上地幔源区具有典型的MORB型源区特征，以辉石巨晶为代表；地幔包体的^3He／^4He值较低，可能是地幔流体交代作用造成的；大陆碱性玄武岩具有与大洋玄武岩截然不同的He同位素组成，反映了大陆区地幔岩浆上升过程中受到了陆壳物质混染。地幔源区^40Ar／^36Ar值为350左右，二辉橄榄岩和碱性火山岩的^40Ar／^36Ar值比大气略高，可能有大气组分的混合。部分样品中有^21Ne、^22Ne、^129Xe、^134Xe和^136Xe相对于大气的过剩现象，是核成因造成的。     

Age structure and recharge conditions of a coastal aquifer (northern Germany) investigated with 39Ar, 14C, 3H, He isotopes and Ne

A tide-influenced two-layer aquifer system in northern Germany was investigated using environmental dating tracers (³H, ³⁹Ar, ¹⁴C), the noble gas isotopes ³He, ⁴He and Ne. The study area is a marshland at the River Ems estuary, exposed to regular flooding until?AD 1000. The construction of dykes, artificial land drainage and groundwater abstraction define the hydraulic gradient. The aquifer depicts a pronounced age stratification with depth. Tritium concentrations above 0.03 TU are found only in the top 30?m. Two tritium-free samples between 20 and 30?m depth show ³⁹Ar ages of 130 and 250?years. Below a clay layer?Cabout 50?m below surface level (mbsl)?Call analysed samples are ³⁹Ar free and, thus, older than 900?years. The initial ¹⁴C activities were about 70 pmC. Resulting ¹⁴C ages increase with depth and increase up to 9,000?years, in agreement with minimal ³⁹Ar ages. Concentrations of radiogenic ⁴He correlate with ¹⁴C ages. Samples in a mid-depth range (20?C70 mbsl) show significant gas loss. The gas loss is assigned to recharge in a methane producing environment. Deduced ⁴He ages were used to assign this water to a infiltration period of about AD 1000.