首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 46 毫秒
1.
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   

2.
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   

3.
Mafic and ultramafic intrusions in East Greenland adjacent to the offshore Greenland–Iceland ridge were emplaced 5–9 My after continental breakup at 55 Ma [1]. Rare earth element (REE) concentrations determined by secondary ion mass spectrometry are reported for cumulus clinopyroxene from these intrusions, and the data are used to estimate REE abundance in equilibrium melts using available partitioning data. Estimated equilibrium melts from intrusions have strongly fractionated REE patterns with Nd/Dy(N) in the range 2 to 5.6 and Yb/Dy(N) 0.55 to 0.92, similar to values for coeval basalts. These melts have markedly higher Nd/Dy(N) than earlier breakup related flood basalts. The moderately low Yb/Dy(N) for the post-breakup volcanism is indicative of residual garnet in the source, while their high Nd/Dy(N) ratios can best be explained by aggregating low degree melts from a light-REE-enriched garnet- and spinel-bearing mantle source. We also report He, Sr, and Nd isotopic data for the intrusions. The highest 3He/4He ratios (>10 R/Ra) are found in the samples whose REE data reflect the largest proportion of melts from a garnet-bearing source, and having Sr and Nd isotopic compositions identical with the radiogenic Sr and unradiogenic Nd isotope end of the Iceland compositional field. There is no indication of a MORB-type mantle in the source of the intrusions. We postulate that post-breakup volcanism along the East Greenland coastline reflects the increasing proximity of the mantle plume to the East Greenland continental margin. The low degree of melting at high mean pressure inferred for the parental melts for the intrusions may reflect re-thickening of the lithosphere, which in turn was caused by the vigorous volcanism during breakup, with accompanying depletion of upper mantle and underplating of the crust at the continental margin.  相似文献   

4.
Helium isotope geochemistry of some volcanic rocks from Saint Helena   总被引：6，自引：0，他引：6  
3He/4He ratios have been measured for olivine and clinopyroxene phenocrysts in 7–15 m.y. old basaltic lavas from the island of St. Helena. Magmatic helium was effectively resolved from post-eruptive radiogenic helium by employing various extraction techniques, includingin vacuo crushing, and stepwise heating or fusion of the powders following crushing. The inherited3He/4He ratio at St. Helena is 4.3–5.9 RA. Helium isotope disequilibrium is present within the phenocrysts, with lower3He/4He upon heating and fusion of the powders following crushing, due to radiogenic ingrowth or to -particle implantation from the surrounding(U + Th)-rich lavas.

A single crushing analysis for clinopyroxene in a basalt from Tubuaii gave3He/4He= 7.1 RA.3He/4He ratios at St. Helena and Tubuaii (HIMU hotspots characterized by radiogenic Pb isotope signatures) are similar to3He/4He ratios previously measured at Tristan da Cunha and Gough Island (EM hotspots characterized by low206Pb/204Pb). Overall, the HeSrPb isotope systematics at these islands are consistent with a mantle origin as contiguous, heterogeneous materials, such as recycled crust and/or lithosphere.3He/4He ratios at HIMU hotspots are similar to mantle xenoliths which display nearly the entire range of Pb isotope compositions found at ocean islands, and are only slightly less than values found in mid-ocean ridge basalts (7–9 RA). This suggests that the recycled materials were injected into the mantle within the last 109 yrs.  相似文献   


5.
A key requirement for any model of mantle evolution is accounting for the high 3He/4He ratios of many ocean island basalts compared to those of mid-ocean ridge basalts. The early, popular paradigm of primitive, undegassed mantle stored in a convectively isolated lower mantle is incompatible with geophysical constraints that imply whole mantle convection. Thus it has been suggested more recently that domains with high 3He/U ratios have been created continuously from the bulk mantle throughout Earth history. Such models require that the 3He/4He ratio of the convecting mantle was at least as high as the highest values seen in OIB at the time the OIB source was generated. These domains must also be created with sufficient He to impart distinctive He isotopic signatures to ocean island basalts. However, the He isotope evolution of the mantle has not been consistently quantified to determine if such scenarios are plausible.

Here a simple model of the He evolution of the whole mantle is examined. Using a wide range of possible histories of continental extraction and He degassing, the bulk convecting mantle was found to have had 3He/4He ratios as high as those seen in the Iceland hotspot only prior to 3 Ga. Such high 3He/4He ratios can only be preserved if located in domains that are not modified by convective mixing or diffusive homogenisation since that time. Further, there are difficulties in producing, with commonly invoked magmatic processes, domains with sufficiently high 3He/U ratios and enough 3He to be able to impart this signature to ocean island basalts. The results are consistent with models that store such He signatures in the core or a deep layer in the mantle, but are hard to reconcile with models that continuously generate high 3He/4He domains within the mantle.  相似文献   


6.
We report new helium isotope results for 49 basalt glass samples from the Mid-Atlantic Ridge between 1°N and 47°S.3He/4He in South Atlantic mid-ocean ridge basalts (MORB) varies between 6.5 and 9.0 RA (RA is the atmospheric ratio of1.39 × 10−6), encompassing the range of previously reported values for MORB erupted away from high3He/4He hotspots such as Iceland. He, Sr and Pb isotopes show systematic relationships along the ridge axis. The ridge axis is segmented with respect to geochemical variations, and local spike-like anomalies in3He/4He, Pb and Sr isotopes, and trace element ratios such as(La/Sm)N are prevalent at the latitudes of the islands of St. Helena, Tristan da Cunha and Gough to the east of the ridge. The isotope systematics are consistent with injection beneath the ridge of mantle “blobs” enriched in radiogenic He, Pb and Sr, derived from off-axis hotspot sources. The variability in3He/4He along the ridge can be used to refine the hotspot source-migrating-ridge sink model.

MORB from the 2–7°S segment are systematically the least radiogenic samples found along the mid-ocean ridge system to date. Here the depleted mantle source is characterized by87Sr/86Sr of 0.7022, Pb isotopes close to the geochron and with206Pb/204Pb of 17.7, and3He/4He of 8.6–8.9 RA. The “background contamination” of the subridge mantle, by radiogenic helium derived from off-ridge hotspots, displays a maximum between 20 and 24°S. The HePb and HeSr isotope relations along the ridge indicate that the3He/4He ratios are lower for the hotspot sources of St. Helena, Tristan da Cunha and Gough than for the MORB source, consistent with direct measurements of3He/4He ratios in the island lavas. Details of the HeSrPb isotope systematics between 12 and 22°S are consistent with early, widespread dispersion of the St. Helena plume into the asthenosphere, probably during flattening of the plume head beneath the thick lithosphere prior to continental breakup. The geographical variation in theHe/Pbratio deduced from the isotope systematics suggests only minor degassing of the plume during this stage. Subsequently, it appears that the plume component reaching the mid-Atlantic ridge was partially outgassed of He during off-ridge hotspot volcanism and related melting activity.

Overall, the similar behavior of He and Pb isotopes along the ridge indicates that the respective mantle sources have evolved under conditions which produced related He and Pb isotope variations.  相似文献   


7.
A detailed study of the geochemistry of a new suite of early Iceland plume picrites shows that extremely high 3He/4He ratios (up to 50 Ra) are found in picrites from Baffin Island and West Greenland. High 3He/4He picrites display a wide range in 87Sr/86Sr (0.70288–0.70403), 143Nd/144Nd (0.51288–0.51308) and incompatible trace element ratios (e.g. La/Smn = 0.5–1.6). These overlap the complete range of compositions of mid-ocean ridge basalts and most northern hemisphere ocean island basalts, including Iceland. Crustal contamination modelling in which high-grade Proterozoic crustal basement rocks for the region are mixed with a depleted parent cannot account for the trend displayed by the Baffin Island and West Greenland picrites. This rules out the possibility that the incompatible trace element, Sr and Nd isotope range of the high 3He/4He picrites is due to crustal contamination. The compositional range at high 3He/4He is also inconsistent with derivation from a primordial-He-rich reservoir that is a residue of ancient mantle depletion. This implies that the composition of the high 3He/4He mantle cannot be determined simply by extrapolating ocean island basalt He–Sr–Nd–Pb–Os isotope data.The apparent decoupling of He from trace element and lithophile radiogenic isotope tracers is difficult to attain by simple mixing of a high-[He], high 3He/4He reservoir with various depleted and enriched He-poor mantle reservoirs. The possibility that primordial He has diffused into a reservoir with a composition typical of convecting upper mantle cannot be ruled out. If so, the process must have occurred after the development of existing mantle heterogeneity, and requires the existence of a deep, primordial He-rich reservoir.  相似文献   

8.
Along the two volcanic off-rift zones in Iceland, the Snfellsnes volcanic zone (SNVZ) and the South Iceland volcanic zone (SIVZ), geochemical parameters vary regularly along the strike towards the centre of the island. Recent basalts from the SNVZ change from alkali basalts to tholeiites where the volcanic zone reaches the active rift axis, and their87Sr/86Sr andTh/U ratios decrease in the same direction. These variations are interpreted as the result of mixing between mantle melts from two distinct reservoirs below Snfellsnes. The mantle melt would be more depleted in incompatible elements, but witha higher3He/4He ratio (R/Ra≈ 20) beneath the centre of Iceland than at the tip of the Snfellsnes volcanic zone (R/Ra≈ 7.5).

From southwest to northeast along the SIVZ, the basalts change from alkali basalts to FeTi basalts and quartz-normative tholeiites. TheTh/U ratio of the Recent basalts increases and both (230Th/232Th) andδ18O values decrease in the same direction. This reflects an important crustal contamination of the FeTi-rich basalts and the quartz tholeiites. The two types of basalts could be produced through assimilation and fractional crystallization in which primary alkali basaltic and olivine tholeiitic melts ‘erode’ and assimilate the base of the crust. The increasingly tholeiitic character of the basalts towards the centre of Iceland, which reflects a higher degree of partial melting, is qualitatively consistent with increasing geothermal gradient and negative gravity anomaly.

The highest Sr isotope ratio in Recent basalts from Iceland is observed inÖrfajökull volcano, which has a3He/4He ratio (R/Ra≈ 7.8) close to the MORB value, and this might represent a mantle source similar to that of Mauna Loa in Hawaii.  相似文献   


9.
Helium isotope characteristics of Andean geothermal fluids and lavas   总被引：10，自引：0，他引：10  
The first comprehensive helium isotope survey of the Andes is reported here. We have sampled geothermal fluids and phyric lava flows from the Southern (svz) and Central (cvz) Volcanic Zones, the volcanically active Pun˜a region and the Precordillera, Salta Basin, Longitudinal Valley and the aseismic region between the two volcanic zones. Although the active areas are characterised by significant differences in crustal age and thickness, the svz, cvz and Pun˜a are characterised by a wide and overlapping range in 3He/4He ratios (for fluids and phenocrysts) from predominantly radiogenic values to close to the MORB ratio. The measured ranges in 3He/4He ratios (R) (reported normalised to the air 3He/4He—RA) are: svz (0.18 < R/RA< 6.9); cvz (0.82 < R/RA< 6.0); and Pun˜a (1.8 < R/RA< 5.4). Modification of magmatic 3He/4He ratios by water/rock interactions (fluids) or post-eruptive grow-in of radiogenic 4He or preferential diffusive loss of 3He (phenocrysts) is considered unlikely; this means that the wide range reflects the helium isotope characteristics of magma bodies in the Andean crust. The mechanism controlling the 3He/4He ratios appears to be a mixing between mantle (MORB-like) helium and a radiogenic helium component derived from radioactive decay within the magma (magma aging) and/or interaction with 4He-rich country rock: a process expected to be influenced by pre-eruptive degassing of the mantle component. Assimilation of lower crust is also capable of modifying 3He/4He ratios, albeit to a much lesser extent. However, it is possible that the highest measured values in each zone were established by the addition of lower crustal radiogenic helium to MORB helium. In this case, the higher ‘base level’ ratios of the svz would reflect the younger crustal structure of this region. In contrast to helium, there is no overlap in the Sr or Pb isotope characteristics of lavas from the active zones: in all areas, therefore, 3He/4He ratios appear to vary independently of Sr and Pb isotope variations. This decoupling between the lithophile tracers and helium reflects the different processes controlling their isotopic characteristics: crust-mantle interactions, alone, for Sr and Pb but for helium the effects of pre-eruptive degassing and possibly magma aging are possibly superimposed. The presence of mantle helium in the Pun˜a region, and to a lesser extent in the Salta Basin, gives an across-arc perspective to the helium isotope distribution and shows mantle melting to occur significantly to the east of the active arc: this is most probably a consequence of lithospheric delamination. The Precordillera hot spring water has the only pure radiogenic helium signal of the entire sample suite and thus marks the western limit of asthenospheric mantle under the Andes.  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.
Abstract Isotopic compositions of He, Ne and Ar were measured on Plio–Quaternary alkaline basalts of Marib–Sirwah and Shuqra volcanic fields in Yemen, south-western Arabian Peninsula. Very high 3He/4He isotope ratios were found in olivine phenocrysts of some Quaternary alkaline basalts in both volcanic fields, located on the margin of the dispersed Afar mantle plume, compared with the Afar–Ethiopian province in the center of the mantle plume. This suggests that the Afar mantle plume source may consist of common component (C or focal zone (FOZO)) with variable primordial 3He/4He ratio rather than high μ mantle (HIMU) component. The three component mixing C as the Afar mantle plume, depleted mantle (DM) as upper mantle and lithospheric mantle with a hybrid enriched mantle I–II (EM I–EM II) characteristics may be adequate to explain He–Sr–Nd–Pb isotope variation for the Afar–Arabian Cenozoic volcanics. The occurrence of high 3He/4He ratios in the Marib–Sirwah volcanic field appears to show that the primitive basaltic magma, derived from the margin of the dispersed trous-like Afar mantle plume during 15–0 Ma, was not by contamination of lithospheric and upper mantle materials in comparison with that from the center of the Afar mantle plume as a result of relatively low thermal anomaly.  相似文献   

12.
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   

13.
Paleocene volcanic rocks in West Greenland and Baffin Island were among the first products of the Iceland mantle plume, forming part of a larger igneous province that is now submerged beneath the northern Labrador Sea. A 40Ar/39Ar dating study shows that volcanism commenced in West Greenland between 60.9 and 61.3 Ma and that 80% of the Paleocene lava pile was erupted in 1 million years or less (weighted mean age of 60.5±0.4 Ma). Minimum estimates of magma production rates (1.3×10−4 km3 year−1 km−1) are similar to the present Iceland rift, except for the uppermost part of the Paleocene volcanic succession where the rate decreases to <0.7×10−4 km3 year−1 km−1 (rift). The timing of onset of volcanism in West Greenland coincides with the opening of the northern Labrador Sea and is also strikingly similar to the age of the oldest Tertiary volcanic rocks from offshore SE Greenland and the British–Irish province. This is interpreted as manifesting the impact and rapid (>1 m/year) lateral spreading of the Iceland plume head at the base of the Greenland lithosphere at 62 Ma. We suggest that the arrival, or at least a major increase in the flux, of the Iceland mantle plume beneath Greenland was a contributing factor in the initiation of seafloor spreading in the northern Labrador Sea. Our study has also revealed a previously unrecognised Early Eocene volcanic episode in West Greenland. This magmatism may be related to movement on the transform Ungava Fault System which transferred drifting from the Labrador Sea to Baffin Bay. A regional change in plate kinematics at 55 Ma, associated with the opening of the North Atlantic, would have caused net extension along parts of this fault. This would have resulted in decompression and partial melting of the underlying asthenosphere. The source of the melts for the Eocene magmatism may have been remnants of still anomalously hot Iceland plume mantle which were left stranded beneath the West Greenland lithosphere in the Early Paleocene.  相似文献   

14.
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   

15.
Over the last two decades great strides have been made in characterizing the spatial distribution, time sequence,geochemical characteristics, mantle sources, and magma evolution processes for various igneous rocks in the Early Permian Tarim Large Igneous Province(TLIP). This work has laid a solid foundation for revealing the evolutionary processes and genetic models of large igneous provinces(LIPs). This study systematically demonstrates the two-stage melting model for the TLIP based on our previous research work and predecessor achievements, and highlights the two types of magmatic rocks within the TLIP.The two-stage melting model suggests that the formation of the TLIP is mantle plume related. The early hot mantle plume caused the low-degree partial melting of the lithosphere mantle, while in the later stage, the plume partially melted due to adiabatic uplift and decompression. Therefore, this model carries signatures of both the "Parana" and "Deccan" models in terms of mantle plume activity. During the early stage, the mantle plume provided the heat required for partial melting of sub-continental lithosphere mantle(SCLM), similar to the "Parana Model", while later the plume acted as the main avenue for melting, as in the "Deccan Model". Basalts that erupted in the first stage have higher 87Sr/86 Sr, lower 143Nd/144 Nd ratios, and are enriched in large ion lithophile elements and high field strength elements, indicating a possible origin from the enriched continental lithosphere mantle,similar to the Parana type geochemical features. The basic-ultrabasic intrusive rocks in the second stage exhibit lower 87Sr/86 Sr,higher 143Nd/144 Nd ratios relative to the basalts, consistent with the involvement of a more depleted asthenospheric material,such as a mantle plume, similar to the Deccan type geochemical features. The first stage basalts can be further subdivided into two categories, i.e., Group 1 and Group 2 basalts. Group 2 basalts have lower 87Sr/86 Sr and higher 143Nd/144 Nd ratios than Group 1 basalts, and lie between compositions of the Group 1 basalts and second stage magmatism. Group 2 basalts may be the intermediate component of the TLIP, and the whole TLIP is the result of plume and lithosphere interaction. Developing this petrogenetic model for the TLIP aids in comprehensively understanding its magmatism and deep geological and geodynamic processes. Furthermore, this work enriches the theories describing the origin of large igneous province and mantle plume activity.  相似文献   

16.
Post-glacial tholeiitic basalts from the western Reykjanes Peninsula range from picrite basalts (oldest) to olivine tholeiites to tholeiites (youngest). In this sequence there are large systematic variations in rare earth element (REE) abundances (La/Sm normalized to chondrites ranges from 0.33 in the picrite basalts to 1.25 in the fissure tholeiites) and corresponding variations in 143Nd/144Nd (0.51317 in the picrite basalts to 0.51299 in the fissure tholeiites). The large viaration in 143Nd/144Nd, more than one-third the total range observed in most ocean islands and mid-ocean ridge basalts (MORB), is accompanied by only a small variation in 87Sr/86Sr (0.7031–0.7032). These 87Sr/86Sr ratios are within the range of other Icelandic tholeiites, and distinct from those of MORB.We conclude that the mantle beneath the Reykjanes Peninsula is heterogeneous with respect to relative REE abundances and 143Nd/144Nd ratios. On a time-averaged basis all parts of this mantle show evidence of relative depletion in light REE. Though parts of this mantle have REE abundances and Nd isotope ratios similar to the mantle source of “normal” MORB, 87Sr/86Sr is distinctly higher. Unlike previous studies we find no evidence for chondritic relative REE abundances in the mantle beneath the Reykjanes Peninsula; in fact, the data require significant chemical heterogeneity in the hypothesized mantle plume beneath Iceland, as well as lateral mantle heterogeneity from the Reykjanes Ridge to the Reykjanes Peninsula. The compositional range of the Reykjanes Peninsula basalts is consistent with mixing of magmas produced by different degrees of melting in different parts of the heterogeneous mantle source beneath the Reykjanes Peninsula.  相似文献   

17.
The isotopic composition of helium emitted from geothermal springs in the southern Tibetan plateau, reported as Rc/RA (Rc=air corrected sample 3He/4He, RA=air 3He/4He), ranges from 0.013 to 0.38, and defines two principal domains. In southernmost central Tibet, helium isotope ratios are typical of radiogenic helium production in the crust (Rc/RA<0.05, crustal helium domain). Further north, there is a resolvable 3He anomaly consistent with a mantle contribution (R/RA>0.1, mantle helium domain). The highest values of 0.27–0.38 RA occur at the southern end of the Karakoram fault. The boundary between the two domains lies 50–100 km north of the Indus-Zangpo suture zone. There seems to be no association between the 3He anomaly and zones of active normal faulting and litho-tectonic crustal units, such as the ultramafic rocks of the Indus-Zangpo suture zone and the Gangdese intrusive belt. Although scavenging of mantle-derived helium, stored in large ultrabasic and basic intrusions in the crust, cannot be ruled out entirely, we argue that the 3He anomaly most plausibly reflects degassing of volatiles from young (Quaternary) mantle-derived melts intruded into the crust. As such, it defines the southern limit of recent mantle melting and mantle melt extraction beneath the Tibetan plateau. The southern limit of the 3He anomaly coincides with the junction between the Indian and Asian plates, in the region where the Indian lithospheric slab steepens and is subducted beneath Tibet as suggested by seismic studies. Recent mantle melting and melt extraction is confined to the Asian mantle, but the southern limit of the melt zone may have migrated northwards during the last 10 Ma as the Indian lithosphere has progressively underthrust the Himalayas and Tibet.  相似文献   

18.
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   

19.
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   

20.
Basalts from young seamounts situated within 6.8 m.y. of the East Pacific Rise, between 9° and 14°N latitude, display significant variations in 143Nd/144Nd (0.51295–0.51321), 87Sr/86Sr (0.7025–0.7031), and(La/Sm)N (0.415–3.270). Nd and Sr isotope ratios are anti-correlated and form a trend roughly parallel to the “mantle array” on a143Nd/144Nd vs.87Sr/86Sr variation diagram. Nd and Sr isotope ratios display negative and positive correlations, respectively, with(La/Sm)N. The geochemical variations observed at the seamounts are nearly as great or greater than those observed over several hundred kilometers of the Reykjanes Ridge, or at the islands of Iceland or Hawaii.

Samples from one particular seamount, Seamount 6, display nearly the entire observed range of chemical variations, offering an ideal opportunity to constrain the nature of heterogeneities in the source mantle. Systematics indicative of magma mixing are recognized when major elements, trace elements, trace element ratios, and isotope ratios are compared with each other in all possible permutations. The source materials required to produce the end-member magmas are: (1) a typical MORB-source-depleted peridotite; and (2) a relatively enriched material which may represent ancient mantle segregations of basaltic melt, incompletely mixed remnants of subducted ocean crust, or metasomatized peridotite such as that found at St. Paul's Rocks or Zabargad Island. Due to the proximity of the seamounts to the East Pacific Rise (EPR), the source materials are thought to comprise an intimate mixture in the mantle immediately underlying the seamounts and the adjacent EPR. Lavas erupted at the ridge axis display a small range of isotopic and incompatible trace element compositions because the large degrees of melting and presence of magma chambers tend to average the chemical characteristics of large volumes of mantle.

If the postulated mantle materials, with large magnitude, small-scale heterogeneities, are ubiquitous in the upper mantle, chemical variations in basalts ranging from MOR tholeiites to island alkali basalts may reflect sampling differences rather than changes in bulk mantle chemistry.  相似文献   


设为首页 | 免责声明 | 关于勤云 | 加入收藏

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