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1.
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   

2.
Noble gas concentrations and isotopic compositions have been determined for four submarine volcanic glasses from the Valu Fa Ridge (VFR) in the southern Lau Basin. The samples are the least differentiated ones from this area, and they display enrichments in fluid-mobile elements similar to the nearby island arc. 3He/4He ratios are slightly below average MORB (6.8–7.8 times atmospheric), whereas Ne, Ar, Kr, and Xe have isotopic compositions very similar to air. Together with previously published data from the Valu Fa Ridge and other spreading segments in the Lau Basin, our data show a systematic latitudinal variation of increasing Ne, Ar, Kr, and Xe abundances from north to south as well as Ne and Ar isotopic compositions changing from MORB-like to atmosphere-like in the same direction. Moreover, isotopic compositions and noble gas abundances of the lavas correlate strongly with Ba/Nb ratios and H2O concentrations. Based on these observations and mass balance arguments, we propose that the atmospheric noble gases come from the subducting oceanic crust and are not due to shallow contamination with air dissolved in seawater or assimilation of old crust. Our data suggest that the noble gases released from the subducting slab are atmospheric and thus contain little or no solar He and Ne. In addition to the fact that ratios of He to heavy noble gases are small in aged ocean crust, He has possibly fractionated from the other noble gases due to its higher diffusivity, and thus He transport from the subducting slab into the mantle wedge is probably insignificant. We propose that the 3He/4He ratios lower than MORB observed in the VFR lavas result from radiogenic ingrowth of He in a highly depleted, and hence degassed, mantle wedge after the enrichment of U and Th released from the downgoing slab.  相似文献   

3.
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   

4.
The troctolites and olivine‐gabbros from the Dive 6 K‐1147 represent the most primitive gabbroic rocks collected at the Godzilla Megamullion, a giant oceanic core complex formed at an extinct spreading segment of the Parece Vela back‐arc basin (Philippine Sea). Previous investigations have shown that these rocks have textural and major elements mineral compositions consistent with a formation through multistage interaction between mantle‐derived melts and a pre‐existing ultramafic matrix. New investigations on trace element mineral compositions basically agree with this hypothesis. Clinopyroxenes and plagioclase have incompatible element signatures similar to that of typical‐MORB. However, the clinopyroxenes show very high Cr contents (similar to those of mantle clinopyroxene) and rim having sharply higher Zr/REE ratios with respect to the core. These features are in contrast with an evolution constrained by fractional crystallization processes, and suggest that the clinopyroxene compositions are controlled by melt‐rock interaction processes. The plagioclase anorthite versus clinopyroxene Mg#[Mg/(Mg + FeTot)] correlation of the Dive 6 K‐1147 rocks shows a trend much steeper than those depicted by other oceanic gabbroic sections. Using a thermodynamic model, we show that this trend is reproducible by fractionation of melts assimilating 1 g of mantle peridotite per 1 °C of cooling. This model predicts the early crystallization of high Mg# clinopyroxene, consistent with our petrological observation. The melt‐peridotite interaction process produces Na‐rich melts causing the crystallization of plagioclase with low anorthite component, typically characterizing the evolved gabbros from Godzilla Megamullion.  相似文献   

5.
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   

6.
The Earth's mantle contains a mixture of primordial noble gases, in particular solar-type helium and neon, and radiogenic rare gases from long-lived U, 232Th, 40K and short-lived 129I, 244Pu. Rocks derived from deep mantle plume magmatism like on Hawaii or Iceland contain a higher proportion of primordial nuclides than rocks from the shallow upper mantle, e.g. mid ocean ridge basalts (MORBs). This is widely regarded as the key evidence for survival of a less degassed and more “primitive” reservoir within the lower mantle. We present an evaluation of noble gas composition showing the shallow mantle to have about five times more radiogenic (relative to primordial) isotopes than Hawaii/Iceland-type plume reservoirs, no matter if short- or long-lived decay systems are considered. This fundamental property suggests that both MORB and plume-type noble gases are mixtures of: (1) a homogeneous radiogenic component present throughout most of the mantle and (2) a uniform primordial noble gas component with very minor radiogenic ingrowth. This conclusion depends crucially on the observed excess of radiogenic Xe in plume-derived rocks, and is only valid if this Xe excess is inherent to the plume sources.Possible sources of the primordial component of mantle plume reservoirs—and possibly also the MORB mantle—could be mantle reservoirs that remained relatively isolated over most of Earth's history (“blobs”, a deep abyssal layer, or the D” layer), but these need a considerable concentration of primordial gases to compensate U, Th, K decay over 4.5 Ga. Earth's core is evaluated as an alternative viable source feeding primordial nuclides into mantle reservoirs: even low metal-silicate partitioning coefficients allow sufficient primordial noble gases to be incorporated into the early forming core, as the undifferentiated proto-Earth was initially gas-rich. Massive mantle degassing soon after core formation then provides the opposite concentration gradient that allows primordial noble gases reentering the mantle at the core-mantle boundary, probably via partial mantle melts. Another possible source of primordial noble gases in Earth's mantle are subducted sediments containing extraterrestrial dust with solar He and Ne, but this supply mechanism crucially depends on largely unconstrained parameters. The latter two scenarios do not require the preservation of a “primitive” mantle reservoir over 4.5 Ga, and can potentially better reconcile increasing geochemical evidence of recycled lithospheric components in mantle plumes and seismic evidence for whole mantle convection.  相似文献   

7.
The Hakusan volcano, central Japan, is located in a region where two subducting plates (the Pacific Plate and the Philippine Sea Plate) overlap near the junction of four plates adjacent to the Japanese Islands (the Pacific Plate, the Philippine Sea Plate, the Eurasia Plate, and the North American Plate). The Hakusan volcano consists of products from four major volcanic episodes: Kagamuro, Ko‐hakusan, and Shin‐Hakusan I and II. To date the eruption events of the Hakusan volcano we applied thermoluminescence and fission track methods. 238U(234U)–230Th disequilibrium and 206Pb/238U methods were applied to date the zircon crystallization ages for estimating the magma residence time before the eruptions. The eruption ages we obtained are ca 250 ka for Kagamuro, ca 100 ka and ca 60 ka for Ko‐Hakusan, ca 50 ka for Shin‐Hakusan I, and <10 ka for Shin‐Hakusan II. They are concordant with previous reports based on K–Ar dating. Some of the pyroclastic rocks, possibly originating from Shin‐Hakusan II activities, are dated to be ca 36 ka or 50 ka, and belong to the Shin‐Hakusan I activity. The zircon crystallization ages show several clusters prior to eruption. The magma residence time was estimated for each volcanic activity by comparing the major crystallization events and eruption ages, and we found a gradual decrease from ca. 500 ky for the Kagamuro activity to ca. 5 ky for the Shin‐Hakusan II activity. This decrease in residence time may be responsible for the decrease in volume of erupted material estimated from the current topography of the region. The scale of volcanic activity, which was deduced from the number of crystallized zircons, is more or less constant throughout the Hakusan volcanic activity. Therefore, the decrease in magma residence time is most likely the result of stress field change.  相似文献   

8.
The tectonic setting of the late mesozoic of South China is in a debate between two schools of thought: an intra‐continental rift zone along a passive continental margin or active rifting associated with subduction of the paleo‐Pacific Plate. In this study, we present new sensitive high‐resolution ion microprobe (SHRIMP) U‐Pb zircon ages, along with geochemical data of three basic dikes that cross‐cut the Dexing porphyry copper deposit. The deposit is the largest of its kind in eastern China and part of large scale mineralization associated with Mesozoic magmatic activity in the area. Our results indicate that the dikes were emplaced in the Late Jurassic with an average U‐Pb age of 153.5 ± 2.4 Ma. The intrusions have bulk εNd(t) of ca +0.7 and zircon εHf(t) value of +1.54 to +6.92. Based on relatively enriched light rare earth elements (LREE) and depleted high‐field‐strength elements (HFSE) abundances with pronounced negative Ta–Nb, Hf–Zr and Ti anomalies in multi‐element diagrams, we propose that these dikes were derived from a subduction‐modified lithospheric mantle source. The variability in Hf isotopes identifies some degree of crustal contaminations. Our data support a scenario with a back‐arc extensional setting or an intra‐arc rift environment associated with the westward subduction of the paleo‐Pacific Plate at or prior to the late Jurassic as the most likely cause for these subduction signatures.  相似文献   

9.
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   

10.
The large differences in He and Ar diffusivities in silicate minerals could result in fractionation of the He/Ar ratio during melting of the mantle, producing He/Ar ratios in the primary mantle melts that are higher than those of the bulk mantle. Modeling noble gas diffusion out of the bulk mantle into fast diffusion pathways (such as fractures or melt channels) suggests that significant (order of magnitude) He/Ar fractionation will occur if the fast diffusion channels are spaced several meters apart and the noble gas residence in these diffusion channels is of the order days to weeks. In addition, the 15% difference in 3He and 4He diffusivities could also produce isotopic fractionation between the melt and its solid source. Modeling the behavior of He and Ar during melting shows that small increases (few %) in 3He/4He should be correlated with larger variations (factor of 5) in 4He/40Ar. However, in order to test this hypothesis the effects of subsequent He–Ar fractionation that occur during degassing have to be corrected. I describe a scheme that can separate He/Ar variations in the primary melt from overprinted fractionation during magmatic degassing. Using the degassing-corrected data, there is a correlation between the primary melt’s 4He/40Ar and 3He/4He in mid-ocean ridge basalts (MORBs). The slope of the correlation is consistent with the models of preferential diffusion of 3He relative to 4He and of 4He relative to 40Ar from the solid mantle into the melt. Diffusive fractionation of noble gases during melting of the mantle can also account for low 4He/40Ar ratios commonly found in residual mantle xenoliths: preferential diffusion of He relative to Ar will produce some regions of the mantle with low 4He/40Ar, the complement of the high 4He/40Ar ratios in basalts. Diffusive fractionation cannot, however, account for differences between the He and Ne isotopic compositions of MORBs compared with ocean island basalts (OIBs); not only are the extremely high 3He/4He ratios of OIBs (up to 50 Ra) difficult to produce at reasonable mantle time and lengthscales, but also the Ne isotopic compositions of MORBs and OIBs do not lie on a single mass fractionation line, therefore cannot result from diffusive fractionation of a single mantle Ne source. If preferential diffusion of He from the solid mantle into primary melts is a significant process during generation of MORBs, then it is difficult to constrain the He concentration of the mantle: He concentrations in basalts and the He flux to the ocean essentially result from extraction of He from a larger (and unknown) volume of mantle than that that produced the basalts themselves. The He concentration of the mantle cannot be constrained until more accurate estimates of the diffusion contribution are available.  相似文献   

11.
Ian Metcalfe 《Island Arc》2016,25(2):126-136
Limestones exposed north of Raub, Pahang, Malaysia, and sandwiched between the Bentong‐Raub Suture Zone and the westernmost margin of the Sukhothai Arc terrane, yield a late Dienerian (late Induan) conodont fauna. The co‐occurrence of Neospathodus dieneri Sweet (morphotypes 1, 2 and 3) and Neospathodus pakistanensis Sweet represents the Neospathodus dieneri morphotype 3 sub‐zone of the Neospathodus dieneri Zone. The sampled limestones are interpreted as the northwards extension of the Jerus Limestone which crops out near Cheroh and Jerus villages, significantly extending the known outcrop of the Jerus Limestone northwards. The Jerus Limestone is interpreted as hemipelagic and formed in a foredeep or forearc setting on top of the accretionary complex formed by eastwards subduction of the Palaeo‐Tethys during the Lower to Middle Triassic.  相似文献   

12.
TheJindingoredeposit,locatedinthenorthwestYunnanProvince,isthelargestPb-Zndeposit(Pb Zn>15Mt1),averagingZn=6.08%andPb/Zn=1/4.7)inChinaatpresent.Toitsnorth,alargeCu-Co-AgdeposithasbeenfoundatBaiyangpingrecently1).TheJindingPb-Zndepositishostedinsandstonesa…  相似文献   

13.
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   

14.
Mesozoic volcanic rocks are widespread throughout the Great Xing'an Range of northeastern China. However, there has been limited investigation into the age and petrogenesis of the Mesozoic volcanics in the eastern Great Xing'an Range. According to our research, the volcanic rocks of the Dayangshu Basin, eastern Great Xing'an Range are composed mainly of trachybasalt, basaltic andesite, and basaltic trachyandesite, with minor intermediate–basic pyroclastic rocks. In this study, the geochemistry and geochronology of the Mesozoic volcanic rocks are presented in order to discuss the petrogenesis and tectonic setting of the Ganhe Formation in the Dayangshu Basin. Zircon U–Pb dating by laser ablation inductively coupled plasma–mass spectrometry indicates that the Mesozoic lavas formed during the late Early Cretaceous (114.3–108.8 Ma). This suite of rocks exhibits a range of geochemical signatures indicating subduction‐related genesis, including: (i) calc‐alkaline to high‐K calc‐alkaline major element compositions; (ii) enrichment of large ion lithophile elements (e.g. Rb, Ba, K) and light rare earth elements (LREEs/HREEs =7.33–9.85); and (iii) weak depletion in high field strength elements (e.g. Nb, Ta, Ti). Furthermore, Sr–Nd–Pb isotopic data yield initial 87Sr/86Sr values of 0.70450–0.70463, positive εNd(t) values of +1.8 to +3.3, and a mantle‐derived lead isotope composition. Combined with the regional tectonic evolution, the results of this study suggest that the Ganhe Group lavas are derived from decompression melting of a metasomatized (enriched) lithospheric mantle, related to asthenospheric upwelling, which resulted from lithospheric mantle delamination and produced extension of the continental margin following the subduction of the Paleo‐Pacific Plate.  相似文献   

15.
The Chilas Complex is a major lower crustal component of the Cretaceous Kohistan island arc and one of the largest exposed slices of arc magma chamber in the world. Covering more than 8000 km2, it reaches a current tectonic width of around 40 km. It was emplaced at 85 Ma during rifting of the arc soon after the collision of the arc with the Karakoram plate. Over 85% of the Complex comprises homogeneous, olivine‐free gabbronorite and subordinate orthopyroxene–quartz diorite association (MGNA), which contains bodies of up to 30 km2 of ultramafic–mafic–anorthositic association (UMAA) rocks. Primary cumulate textures, igneous layering, and sedimentary structures are well preserved in layered parts of the UMAA in spite of pervasive granulite facies metamorphism. Mineral analyses show that the UMAA is characterized by more magnesian and more aluminous pyroxene and more calcic plagioclase than those in the MGNA. High modal abundances of orthopyroxene, magnetite and ilmenite (in MGNA), general Mg–Fe–Al spatial variations, and an MFA plot of whole‐rock analyses suggest a calc‐alkaline origin for the Complex. Projection of the pyroxene compositions on the Wo–En–Fs face is akin to those of pyroxenes from island arcs gabbros. The presence of highly calcic plagioclase and hornblende in UMAA is indicative of hydrous parental arc magma. The complex may be a product of two‐stage partial melting of a rising mantle diaper. The MGNA rocks represent the earlier phase melting, whereas the UMAA magma resulted from the melting of the same source depleted by the extraction of the earlier melt phase. Some of the massive peridotites in the UMAA may either be cumulates or represent metasomatized and remobilized upper mantle. The Chilas Complex shows similarities with many other (supra)subduction‐related mafic–ultramafic complexes worldwide.  相似文献   

16.
The Permian–Triassic high pressure metamorphism and potassic magmatism in central Korea attest to the extension of the Dabie‐Sulu collision belt in central‐eastern China towards the Korean Peninsula and possibly the Japanese Islands. We present major and trace element and Sr–Nd isotope data for a ca. 230 Ma monzodiorite pluton emplaced in the Goesan area, central Okcheon belt, Korea. This pluton shows geochemical features comparable with those of the coeval monzonite–syenite–gabbro–mangerite suite documented recently in the Gyeonggi massif. The metaluminous and alkali–calcic signatures of the Goesan intrusives correspond to the Caledonian‐type post‐orogenic granitoids. The K2O/Na2O ratios of all analyzed samples are greater than 1, and are not correlative with their SiO2 contents. The enrichment of both large‐ion‐lithophile elements and highly compatible elements in the Goesan pluton is probably indicative of metasomatized mantle origin. The elemental fractionation in the source region must have occurred in the distant past, possibly the Paleoproterozoic, to generate significantly negative εNd(t) values (< –16). Chondrite‐normalized rare earth element patterns as well as Rb/Sr and Ba/Rb ranges suggest that the source consists of amphibole‐bearing rocks. Progressive decreases in negative Eu anomaly and Ba, Sr, Ni, Cr and V contents with increasing SiO2 contents reflect an important role of plagioclase, biotite and hornblende for the fractionation process. Zr is undersaturated in the potassic, metaluminous melt. The initial Sr–Nd isotopic compositions of the samples are correlated with their SiO2 contents, substantiating a role of crustal assimilation during the magmatic differentiation. The Sr–Nd elemental and isotopic modeling suggests that the Goesan pluton was initially slightly heterogeneous in its isotopic composition, and underwent concurrent assimilation and fractional crystallization. The occurrence of the Goesan pluton provides further evidence corroborating the amalgamation of allochthonous terranes within the Okcheon belt during the Permian–Triassic collisional orogeny.  相似文献   

17.
New noble gas data of ultramafic xenoliths from Réunion Island, Indian Ocean, further constrain the characteristics of primordial and radiogenic noble gases in Earth’s mantle plume reservoirs. The mantle source excess of nucleogenic 21Ne is significantly higher than for the Hawaiian and Icelandic plume reservoirs, similar to excess of radiogenic 4He. 40Ar/36Ar of the Réunion mantle source can be constrained to range between 8000 and 12 000, significant 129Xe and fission Xe excess are present. Regarding the relative contribution of primordial and radiogenic rare gas nuclides, the Réunion mantle source is intermediate between Loihi- and MORB-type reservoirs. This confirms the compositional diversity of plume sources recognized in other radioisotope systematics. Another major result of this study is the identification of the same basic primordial component previously found for the Hawaiian and Icelandic mantle plumes and the MORB reservoir. It is a hybrid of solar-type He and Ne, and ‘atmosphere-like’ or ‘planetary’ Ar, Kr, Xe (Science 288 (2000) 1036). 20Ne/22Ne ratios extend to maximum values close to 12.5 (Ne-B), which is the typical signature of solar neon implanted as solar corpuscular radiation. This suggests that Earth’s solar-type noble gas inventory was acquired by small (less than km-sized) precursor planetesimals that were irradiated by an active early sun in the accretion disk after nebular gas dissipation, or, alternatively, that planetesimals incorporated constituents irradiated in transparent regions of the solar nebula. Previously, such an early irradiation scenario was suggested for carbonaceous chondrites which follow common volatile depletion trends in the sequence CI–CM–CV–Earth. In turn, CV chondrites closely match Earth’s mantle composition in 20Ne/22Ne, 36Ar/22Ne and 36Ar/38Ar. This indicates that mantle Ar could well be a planetary component inherited from precursor planetesimals. However, a corresponding conclusion for mantle Kr and Xe is less convincing yet, but this may be just due to the lack of appropriate ‘meteoritic’ building blocks matching terrestrial composition. Alternatively, heavy noble gases in Earth’s mantle could be due to admixing of severely fractionated air, but this effect must have affected all mantle sources to a very similar extent, e.g. by global subduction before the last homogenization of the mantle reservoirs.  相似文献   

18.
Helium (He) and Argon (Ar) isotopic compositions of the Tertiary basic igneous rocks were determined by the high temperature melting extraction method. The selected samples for the studies included al-kaline basalts and diabases from the Jiyang basin,and the surrounding Shanwang and Qixia outcrops in the Shandong Peninsula,eastern China. The results show that the Paleogene basalts and diabases from the Jiyang basin yielded a wide range of P4 PHe abundance of (73.70-804.16)×10 P-8 Pcm P3 P STP·g P-1 P,with P3 PHe/ P4 PHe ratios of 0.374-2.959 Ra,which was lower than the MORB but evidently higher than the con-tinental crust value. The Neogene alkaline basalts from the Jiyang basin,Shanwang and Qixia outcrops have variable P4 PHe abundances ((42.34-286.72)×10-8 Pcm P3 P STP·g-1 P),and "continental crust-like" P3 PHe/ P4 PHe ratios (0.013-0.074 Ra). All of them contain atmospheric-like P40 PAr/ P36 PAr ratio (395.4-1312.7),reflecting the mantle sources with air components. Their low P3 PHe/ P4 PHe ratios are interpreted as the enrichment of the radiogenic P4 PHe mainly inherited from the mantle. He and Ar systematics show the mixing of MORB-type,air and a P4 PHe enriched member in the mantle source,suggesting that these igneous rocks originated from the depleted asthenospheric mantle mixed with an EMI component. Therefore,the present He and Ar isotopes do not support the viewpoints that the Cenozoic igneous rocks of Eastern North China were the products of mantle plume(s) activities.  相似文献   

19.
The relationships between the major terrestrial volatile reservoirs are explored by resolving the different components in the Xe isotope signatures displayed by Harding County and Caroline CO2 well gases and mid-ocean ridge basalts (MORB). For the nonradiogenic isotopes, there is evidence for the presence of components enhanced in the light 124–128Xe/130Xe isotope ratios with respect to the terrestrial atmosphere. The observation of small but significant elevations of these ratios in the MORB and well gas reservoirs means that the nonradiogenic Xe in the atmosphere cannot be the primordial base composition in the mantle. The presence of solar-like components, for example U–Xe, solar wind Xe, or both, is required.For radiogenic Xe generated by decay of short-lived 129I and 244Pu, the 129Xerad/136Xe244 ratios are indistinguishable in MORB and the present atmosphere, but differ by approximately an order of magnitude between the MORB and well gas sources. Correspondence of these ratios in MORB and the atmosphere within the relatively small uncertainties found here significantly constrains possible mantle degassing scenarios. The widely held view that substantial early degassing of 129Xerad and 136Xe244 from the MORB reservoir to the atmosphere occurred and then ended while 129I was still alive is incompatible with equal ratios, and so is not a possible explanation for observed elevations of 129Xe/130Xe in MORB compared to the atmosphere. Detailed degassing chronologies constructed from the isotopic composition of MORB Xe are therefore questionable.If the present estimate for the uranium/iodine ratio in the bulk silicate Earth (BSE) is taken to apply to all interior volatile reservoirs, the differing 129Xerad/136Xe244 ratios in MORB and the well gases point to two episodes of major mantle degassing, presumably driven by giant impacts, respectively  20–50 Ma and  95–100 Ma after solar system origin assuming current values for initial 129I/127I and 244Pu/238U. The earlier time range, for degassing of the well gas source, spans Hf–W calculations for the timing of a moon-forming impact. The second, later impact further outgassed the upper mantle and MORB source. A single event that degassed both the MORB and gas well reservoirs at the time of the moon-forming collision would be compatible with their distinct 129Xerad/136Xe244 ratios only if the post-impact iodine abundance in the MORB reservoir was about an order of magnitude lower than current estimates. In either case, such late dates require large early losses of noble gases, so that initial inventories acquired throughout the Earth must have been substantially higher.The much larger 129Xerad/136Xe244 ratio in the well gases compared to MORB requires that these two Xe components evolve from separate interior reservoirs that have been effectively isolated from each other for most of the age of the planet, but are now seen within the upper mantle. These reservoirs have maintained distinct Xe isotope signatures despite having similar Ne isotope compositions that reflect similar degassing histories. This suggests that the light noble gas and radiogenic Xe isotopes are decoupled, with separate long-term storage of the latter. However, without data on the extent of heterogeneities within the upper mantle, this conclusion cannot be easily reconciled with geophysical observations without significant re-evaluation of present noble gas models. Nevertheless the analytic evidence that two different values of 129Xerad/136Xe244 exist in the Earth appears firm. If the uranium/iodine ratio is approximately uniform throughout the BSE, it follows that degassing events from separate reservoirs at different times are recorded in the currently available terrestrial Xe data.  相似文献   

20.
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   

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