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1.
We report isotope analyses of helium, neon, argon, and xenon using different extraction techniques such as stepwise dynamic and static crushing, and high-resolution stepwise heating of three mantle xenoliths from Réunion Island. He and Ne isotopic compositions were similar to previously reported Réunion data, yielding a more radiogenic composition when compared to the Hawaiian or Icelandic mantle plume sources. We furthermore observed correlated 129Xe/130Xe and 136Xe/130Xe ratios following the mantle trend with maximum values of 6.93 ± 0.14 and 2.36 ± 0.06, respectively. High-resolution argon analyses resulted in maximum 40Ar/36Ar ratios of 9000–11,000, in agreement with maximum values obtained in previous studies. We observed a well-defined hyperbolic mixing curve between an atmospheric and a mantle component in a diagram of 40Ar/36Ar vs. 20Ne/22Ne. Using a mantle 20Ne/22Ne of 12.5 (Ne–B) a consistent 40Ar/36Ar value of 11,053 ± 220 in sample ILR 84-4 was obtained, whereas extrapolations to a higher mantle 20Ne/22Ne ratio of 13.8 (solar wind) would lead to a much higher 40Ar/36Ar ratio of 75,000, far above observed maximum values. This favours a mantle 20Ne/22Ne of about 12.5 considered to be equivalent to Ne–B. Extrapolated and estimated 40Ar/36Ar ratios of the Réunion, Iceland, Loihi, and MORB mantle sources, respectively, tend to be linearly correlated with air corrected 21Ne/22Ne and show the same systematic sequence of increasing relative contributions in radiogenic isotopes (Iceland–Loihi–Réunion–MORB) as observed for 4He/3He. In general, He–Ne–Ar isotope systematics of the oceanic mantle can be explained by following processes: (i) different degree of mixing between pure radiogenic and pure primordial isotopes generating the MORB and primitive plume (Loihi-type) endmembers; (ii) relatively recent fractionation of He relative to Ne and Ar, in one or both endmembers; (iii) after the primary fractionation event, different degrees of mixing between melts or fluids of MORB and primitive plume affinity generate the variety of observed OIB data, also on a local scale; (iv) very late-stage secondary fractionation during magma ascent and magma degassing leads to further strong variation in He/Ne and He/Ar ratios.  相似文献   

2.
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   

3.
In an attempt to constrain the origin of polycrystalline diamond, combined analyses of rare gases and carbon and nitrogen isotopes were performed on six such diamonds from Orapa (Botswana). Helium shows radiogenic isotopic ratios of R/Ra = 0.14–1.29, while the neon ratios (21Ne/22Ne of up to 0.0534) reflect a component from mantle, nucleogenic and atmospheric sources. 40Ar/36Ar ratios of between 477 and 6056 are consistent with this interpretation. The (129Xe/130Xe) isotopic ratios range between 6.54 and 6.91 and the lower values indicate an atmospheric component. The He, Ne, Ar and Xe isotopic compositions and the Xe isotopic pattern are clear evidence for a mantle component rather than a crustal one in the source of the polycrystalline diamonds from Orapa. The δ13C and δ15N isotopic values of − 1.04 to − 9.79‰ and + 4.5 to + 15.5‰ respectively, lie within the range of values obtained from the monocrystalline diamonds at that mine. Additionally, this work reveals that polycrystalline diamonds may not be the most appropriate samples to study if the aim is to consider the compositional evolution of rare gases through time. Our data shows that after crystallization, the polycrystalline diamonds undergo both gas loss (that is more significant for the lighter rare gases such as He and Ne) and secondary processes (such as radiogenic, nucleogenic and fissiogenic, as well as atmospheric contamination). Finally, if polycrystalline diamonds sampled an old mantle (1–3.2 Ga), the determined Xe isotopic signatures, which are similar to present MORB mantle – no fissiogenic Xe from fission of 238U being detectable – imply either that Xe isotopic ratios have not evolved within the convective mantle since diamond crystallization, or that these diamonds are actually much younger.  相似文献   

4.
Helium, neon, and argon isotopic compositions were measured in two flows of the Columbia River flood basalt. The Imnaha Basalt has a 3He/4He ratio of 11.4 times atmospheric and 20Ne/22Ne and 21Ne/22Ne ratios characteristic of a plume component. The measured 3He/4He is a lower limit, due to possible preferential 3He loss and/or addition of radiogenic 4He. A Wanapum Basalt flow, erupted approximately 2 Ma later in the waning stages of volcanism, has more MORB-like noble gases. The He, Nd and Sr isotopic compositions of these lavas suggest that the Columbia River basalts were derived from the Yellowstone plume head which contained both ‘high-helium’ plume material and entrained depleted mantle. As the eruptions progressed the plume component in the melting region was gradually diluted or replaced.  相似文献   

5.
Noble gas systematics of deep rift zone glasses from Loihi Seamount, Hawaii   总被引：3，自引：0，他引：3  
We report new noble gas fusion and crushing data for six pillow rim glasses, recovered between 3 and 5 km water depth on the south rift zone of Loihi Seamount, Hawaii. Helium abundances of the glasses vary from 0.3 to 2.3 μcc/g, with 4He/3He ratios between 30000 and 27000 (24–27 RA), similar to previously reported values. The neon data form a correlation line which is similar to the Loihi-Kilauea line reported by Honda et al. [1], but extends to much higher ratios, up to 12.9 and 0.0382 for the 20Ne/22Ne and 21Ne/22Ne ratios, respectively. This provides conclusive evidence for the suggestion that the Hawaiian plume, thought to originate in the lower mantle, has a solar-like 20Ne/22Ne composition [1], but a slightly higher 21Ne/22Ne ratio. 40Ar/36Ar ratios of the deep rift-zone glasses are as high as 2600, and show a positive correlation with neon isotopic ratios. In contrast to neon and argon, all xenon isotopic compositions are isotopically indistinguishable from air, which either suggests preferential atmospheric contamination of xenon, or could indicate an atmospheric xenon isotopic composition for the lower mantle.  相似文献   

6.
Fresh basalt glasses from the North Chile Ridge (NCR) in the southeastern Pacific have Ne isotopic compositions distinctly different from typical mid-ocean ridge basalts (MORB). In a three-isotope plot of 20Ne/22Ne vs. 21Ne/22Ne, the NCR data define a correlation line with a slope smaller than that of the MORB correlation line, i.e. their Ne composition is more nucleogenic than that of MORB. 3He/4He ratios are slightly lower than the MORB average, whereas in a few stepwise heating fractions very high 40Ar/36Ar ratios up to 28,000 are found. One model to explain the data assumes contamination of the NCR mantle source by material from the continental or oceanic crust, but in addition to difficulties with quantitatively reconciling the noble gas patterns with such a model it seems unable to account for some geochemical characteristics of NCR basalts reported earlier [Bach et al., Earth Planet. Sci. Lett. 142 (1996) 223–240], such as depletions in highly incompatible elements and unradiogenic Sr isotope compositions. Therefore we favor the scenario of a mantle source which was depleted and degassed previously, possibly as a residue from mantle melting beneath the southern East Pacific Rise that was transported to the NCR and melted again. The time during which such a depleted reservoir would have to be separated from the MORB mantle is estimated at 10–100 Ma based on U/Th–Ne systematics, in reasonable agreement with the time scale deduced from the formation history of the NCR and the temporal evolution of the southeast Pacific.  相似文献   

7.
186Os enrichments in volcanic rocks and peridotite-derived iridosmine grains have been attributed to contributions from Earth’s outer core to the mantle, and apparently constrain the scale of mantle convection and an early timing for inner–outer core segregation more than 3.5 Gyr ago. Here, we highlight that marine ferromanganese crusts and nodules are characterised by high Pt/Os ratios and Pt–Os contents that develop much larger 186Os excesses over geological time (≥0.2%/Gyr) than those hypothesised for Earth’s outer core (<0.005–0.01%/Gyr). 187Os/188Os ratios in ferromanganese crusts are radiogenic due to sequestering of continental Os from seawater. Similarly, ancient ferromanganese materials may have had 186Os excesses (>0.1%) as a result of high Pt/Os ratios in continental crust, even prior to in-growth of 186Os after formation due to their high Pt/Os ratios. Past recycling of small amounts of these materials into the Earth’s mantle will produce coupled 187Os–186Os excesses and little change in Re and platinum-group-element concentrations, as observed in Hawaiian picrites, and in contrast to the predicted result of outer core addition to the mantle. 187Os and 186Os enrichments in the Hawaiian mantle source are potentially consistent with it comprising recycled oceanic lithosphere, pelagic sediments and ferromanganese materials, and questions the notion that Os isotopes can be used to uniquely identify core–mantle interactions and the depth at which mantle sources for volcanism originate.  相似文献   

8.
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   

9.
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   

10.
Noble gas elemental and isotopic abundances have been analysed in eight samples of youthful basaltic glass dredged from three different locations within the Lau Backarc Basin: (1) the King's Triple Junction, (2) the Central Lau Spreading Centre at 18°S and (3) the Eastern Lau Spreading Centre at 19°S. Samples from the Lau central and eastern spreading centres have MORB-like helium isotopic ratios of approximately 1.2 × 10−5 (8.5 R/RA). In contrast, the samples from the King's Triple Junction yield helium isotopic ratios averaging 9.4 (±0.8) × 10−6 (6.7 ± 0.6 R/RA), systematically lower than the MORB-like value, which may be reflecting the addition of radiogenic 4He released from the descending slab. Neon isotopic ratios are enriched in 20Ne and 21Ne with respect to atmospheric ratios by as much as 23% and 62% respectively. These observations further confirm that non-atmospheric neon is a common characteristic of samples derived from the mantle. The helium and neon isotopic signatures in the samples can be explained by mixing of a primordial solar component, radiogenic and nucleogenic components produced by radioactive processes inside the Earth, and an atmospheric component. This reconnaissance survey of noble gases in a backarc basin indicates that current volcanism is dominated by magmas from the mantle wedge, a source similar to that from which MORBs are derived. The heavier noble gases (argon, krypton and xenon), however, show more atmosphere-like compositions, either indicating strong interaction of the magmas with the atmosphere or the presence of a recycled component derived from the underlying subducting slab.  相似文献   

11.
Abstract Elemental and isotopic compositions of noble gases extracted from the bore hole water in Osaka plain, central Japan were examined. The water samples were collected from four shallow bore holes (180-450 m) and seven deep bore holes (600-1370 m) which have been used for an urban resort hot spring zone. The water temperatures of the deep bore holes were 22-50°C and that of the shallow bore holes, 13-23°C. The elemental abundance patterns show the progressive enrichment of the heavier noble gases compared with the atmospheric noble gas composition except for He, which is heavily enriched in deep bore hole water samples. 3He/4He ratios from the bore holes reaching the Ryoke granitic basement were higher than the atmospheric value (1.4 × 10−6), indicating a release of mantle He through the basement. The highest value of 8.2 × 10−6 is in the range of arc volcanism. On the other hand, the bore holes in sedimentary rocks overlying the basement release He enriched in radiogenic 4He, resulted in a low 3He/4He ratio of 0.5 × 10−6. 4He/20Ne and 40Ar/36Ar ratios indicate that the air contamination is generally larger in shallow bore holes than in deep ones from each site. The helium enriched in mantle He is compatible with the previous work which suggested up-rising magma in 'Kinki Spot', the area of Osaka and western Wakayama, in spite of no volcanic activity in the area. A model to explain an initiation of magma generation beneath this area is presented.  相似文献   

12.
Picrites from the 61 million year old Vaigat Formation of the Nuussuaq Peninsula in West Greenland have 3He/4He ratios trapped in olivine phenocrysts which range up to 30 times the atmospheric ratio. These high values, measured during gas extraction by crushing in vacuum, are similar to the highest magmatic 3He/4He ratios found in young terrestrial volcanic rocks. By analogy with young basalts, in which crushing selectively extracts magmatic helium, any significant cosmogenic 3He appears to be absent in these picrites. Additional evidence for the absence of cosmogenic helium is provided by fusion results on the crushed olivine powders and by a single stepwise crushing experiment, in which only magmatic and radiogenic helium components are resolvable. The West Greenland picrites have Pb, Nd and Sr isotope compositions which overlap those found in picrites from Iceland and in basalts from Loihi Seamount, localities which today also have high 3He/4He ratios. Isotopic variations in He, Pb, Nd and Sr for the West Greenland picrites are interpreted to largely result from interaction of the early Iceland mantle plume with the upper mantle during plume ascent and dispersion beneath the continental lithosphere. The presence of high 3He/4He ratios in West Greenland, and the onset of magmatism across the North Atlantic Volcanic Province near 62 Ma, supports the hypothesis for very rapid dispersion (>1 m/year) of mantle plume head material during the earliest stages of plume impact, as predicted in recent numerical simulations of plume behavior during thermal mantle convection with non-Newtonian rheology.  相似文献   

13.
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   

14.
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   

15.
本文分别在直角坐标系和柱坐标系下,研究瑞利数从104逐渐增大到107对热对流的影响,数值计算结果表明:瑞利数越大,地幔柱越窄,地幔柱上升速度也越快;源自上地幔的地幔柱半径的范围为9到210 km.根据峨眉山内带的半径推算出地幔的黏性系数约为3.8×1021Pa·s,地幔柱平均流动速度为2.5 cm/a.  相似文献   

16.
Chemical and isotopic ratio (He, C, H and O) analysis of hydrothermal manifestations on Pantelleria island, the southernmost active volcano in Italy, provides us with the first data upon mantle degassing through the Sicily Channel rift zone, south of the African–European collision plate boundary. We find that Pantelleria fluids contain a CO2–He-rich gas component of mantle magmatic derivation which, at shallow depth, variably interacts with a main thermal (100°C) aquifer of mixed marine–meteoric water. The measured 3He/4He ratios and δ13C of both the free gases (4.5–7.3 Ra and −5.8 to −4.2‰, respectively) and dissolved helium and carbon in waters (1.0–6.3 Ra and −7.1 to −0.9‰), together with their covariation with the He/CO2 ratio, constrain a 3He/4He ratio of 7.3±0.1 Ra and a δ13C of ca. −4‰ for the magmatic end-member. These latter are best preserved in fluids emanating inside the active caldera of Pantelleria, in agreement with a higher heat flow across this structure and other indications of an underlying crustal magma reservoir. Outside the caldera, the magmatic component is more affected by air dilution and, at a few sites, by mixing with either organic carbon and/or radiogenic 4He leached from the U–Th-rich trachytic host rocks of the aquifer. Pantelleria magmatic end-member is richer in 3He and has a lower (closer to MORB) δ13C than all fluids yet analyzed in volcanic regions of Italy and southern Europe, including Mt. Etna in Sicily (6.9±0.2 Ra, δ13C=−3±1‰). This observation is consistent with a south to north increasing imprint of subducted crustal material in the products of Italian volcanoes, whose He and C (but also O and Sr) isotopic ratios gradually evolve towards crustal values northward of the African–Eurasian plate collision boundary. Our results for Pantelleria extend this regional isotopic pattern further south and suggest the presence of a slightly most pristine or ‘less contaminated’, 3He-richer mantle source beneath the Sicily Channel rift zone. The lower than MORB 3He/4He ratio but higher than MORB CO2/3He ratio of Pantelleria volatile end-member are compatible with petro-geochemical evidence that this mantle source includes an upwelling HIMU–EM1-type asthenospheric plume component whose origin, according to recent seismic data, may be in the lower mantle.  相似文献   

17.
On the basis of the4He/20Ne ratios in feldspathic particles from Apollo 11, basaltic fragments from Apollo 11, and magnetic separates from Apollo 12 fines, one expects the former to have the highest, and the Apollo 12 material to have the lowest84Kr/132Xe ratios. This is not the case; the84Kr/132Xe ratios from sample 12070 are substantially greater than those from the feldspathic and basaltic fragments in 10084. The trend-reversal in the feldspathic particles could be due to the trapping of genuine primordial lunar Kr and Xe. The reversal in the Apollo 11 basaltic fragments might be due to periodicnear-quantitative loss of the lighter gases by impact heating, with the Apollo 11 fines containing a relatively large proportion of strongly heated fragments.  相似文献   

18.
Noble gas isotopes (3He, 4He, Ne, Ar, Kr, Xe), tritium (3H), chlorofluorocarbons (CFCs) and dissolved oxygen (O2) were seasonally measured in a small groundwater system recharged by infiltration of river water at Linsental, northeastern Switzerland. All Groundwater samples contained an excess of atmospheric noble gases (‘excess air’) usually with an elemental composition equal to air. The concentrations of atmospheric noble gases in the groundwater were used to calculate the excess air component and the water temperature at recharge. The noble gas temperatures (NGTs) in the boreholes close to the river vary seasonally, however, the average NGT of all samples lies close to the mean annual temperature of the river water. Groundwater ages were calculated using the tritium/helium-3 (3H/3He) dating method. The water ages of the samples obtained near the river depend on the amount of recently infiltrated river water and are young during times of active river discharge. In contrast, the mean water age of about 3 years of the deep aquifer remained nearly constant over the sampling period. The observed CFC-11 (CFCl3) and CFC-12 (CF2Cl2) concentrations are significantly higher than the atmospheric equilibrium concentrations and therefore CFCs do not provide any direct information on the residence time of the groundwater. Nevertheless, the CFC excess in the groundwater shows a linear increase with the 3H/3He age. Additionally, both accumulation of radiogenic He (4Herad) and O2 consumption are strongly correlated with residence time. All these correlations can be interpreted either in terms of mixing of recently infiltrated river water with older groundwater or in terms of accumulation/consumption rates.  相似文献   

19.
Osmium, strontium, neodymium, and lead isotopic data have been obtained for 30 hand picked samples of basaltic glass from the Pacific, Atlantic and Indian mid-oceanic ridges. Large variations in Os isotopic ratios exist in the glasses, from abyssal peridotite-like values to radiogenic compositions similar to oceanic island basalts (187Os/186Os and 187Os/188Os ratios range from 1.06 to 1.36 and from 0.128 to 0.163, respectively). Os isotopic and elemental data suggest the existence of mixing correlations. This relationship might be ascribed to secondary contamination processes; however, such a hypothesis cannot account for the negative correlation observed between Os and Nd isotopes and the existence of complementary covariations between Os and SrPb isotopes. In this case, OsSrNdPb isotopic variations are unrelated to late post-eruption or shallow level contamination. These relationships provide strong evidence that the Os isotopic composition of the samples are derived from the mantle and thus implies a global chemical heterogeneity of the oceanic upper mantle. The results are consistent with the presence of recycled oceanic crust in the mantle sources of mid-ocean ridge basalts, and indicate that the unique composition of the upper mantle below the Indian ocean results from its contamination by a mantle component characterized by radiogenic Os and particularly unradiogenic Nd and Pb isotopic compositions.  相似文献   

20.
Neon isotopic ratios measured in olivine and basaltic glass from Iceland are the most primitive observed so far in terrestrial mantle-derived samples. Ratios were measured in gas released from olivine and basaltic glass from a total of 10 samples from the Reykjanes Peninsula, Iceland, and one sample from central Iceland. The neon isotopic ratios include solar-like, mid-ocean ridge basalt (MORB)-like and atmospheric compositions. Neon isotopic ratios near the air–solar mixing line were obtained from the total gas released from glass separates from five samples. MORB-like neon isotopic compositions were measured in the total gas released from olivine and glass separates from four samples. Although there is clear evidence for a solar neon component in some of the Icelandic samples, there is no corresponding evidence for a solar helium ratio (320Ra>3He/4He>100Ra). Instead, 3He/4He ratios are mainly between 12±2(Ra) and 29±3(Ra), similar to the range observed in ocean island basalts, indicating that the He–Ne isotopic systematics are decoupled. The mantle source of Icelandic basalts is interpreted to be highly heterogeneous on a local scale to explain the range in observed helium and neon isotopic ratios. The identification of solar-like neon isotopic ratios in some Icelandic samples implies that solar neon trapped within the Earth has remained virtually unchanged over the past 4.5 Ga. Such preservation requires a source with a high [Nesolar]/[U+Th] ratio so that the concentration of solar neon overwhelms the nucleogenic 21Ne* produced from the decay of U and Th in the mantle over time. High [Nesolar]/[U+Th] ratios are unlikely to be preserved in the mantle if it has experienced substantial melting. An essentially undegassed primitive mantle component is postulated to be the host of the solar neon in the Icelandic plume source. Relatively small amounts of this primitive mantle component are likely to mix with more depleted and degassed mantle such that the primitive mantle composition is not evident in other isotopic systems (e.g. strontium and neodymium). The lower mantle plume source is inferred to be relatively heterogeneous owing to being more viscous and less well stirred than the upper mantle. This discovery of near-solar neon isotopic ratios suggests that relatively primitive mantle may be preserved in the Icelandic plume source.  相似文献   

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