Helium isotopes and mantle volatiles in Loihi Seamount and Hawaiian Island basalts and xenoliths

We examine in this paper the use of helium isotope ratios for the study of hotspot volcanism along age-progressive island volcanic chains. The Hawaiian Islands are the original “high ³He” hotspot, with ³He/⁴He ratios as high as 32 × the atmospheric ratio; in the Pacific they stand out against the surrounding sea of MORB (rather uniformly 8 × atmospheric) which fills the entire Pacific with the exception of the Macdonald-Mehetia-Samoa axis in the South Pacific. The recent availability of a variety of alkalic and tholeiitic glasses from the U.S. Geological Survey and our own dredge hauls has prompted us to look first at isotopic variability within a single fresh and new volcano which is probably sitting directly atop a mantle plume. Thus we have looked in some detail at the total helium in glass pillow rims, at He in the enclosed vesicles, and at He in the glass itself, in both tholeiitic and alkalic lavas, and also at helium in associated phenocrysts and xenoliths. The measured ³He/⁴He ratios range from atmospheric to 30 × atmospheric, but we see clear evidence that the highly vesiculated lavas suffer exchange of He between the thin glass walls of vesicles and ambient seawater, so that we observe a post-eruptive isotopic disequilibrium between glass and gas phases. The primary effect is the very large loss of initial He content during eruptive vesiculation, which results in quite large isotopic effects from small additions of ambient He (of the order of 0.02 μcc He per gram of basalt; corresponding to a “water/rock ratio” of 0.5). Phenocrystic He in olivines verifies that the gas-phase He is not affected by vesicularities up to about 5%. Alkali basalt He appears to be independent of vesicularity up to values as high as 35%; this He is somewhat lower in ³He/⁴He ratio, but matches precisely the associated xenolithic He. However, from the present data we cannot exclude the possibility that diffusive exchange with seawater has affected the He ratio in alkalic vesicles.On the large scale, along the 10% of the Hawaiian chain available for subaerial sampling, we find high ³He/⁴He ratios (24 × atmospheric) in 5.5 × 10⁶-year-old lavas on Kauai. Maximum values of the ratio so far observed are in the pre-erosional Kula basalts on Maui, confirming the previous results of Kaneoka and Takaoka. Hawaii, where these high values were first observed is now seen to range from MORB ratios at Mauna Loa to only 15 × R_A at Kilauea fumaroles. Most xenolithic He so far measured is MORB He, but Loihi xenoliths have high values and are quite different in this respect. Finally, we discuss also the hydrogen and carbon isotope results on Loihi lavas, and show that these elements resemble MORB and appear not to show a distinctive plume signature.     

The water content and hydrogen isotope composition of continental lithospheric mantle and mantle-derived mafic igneous rocks in eastern China

The water contents of minerals and whole-rock in mantle-derived xenoliths from eastern China exhibit large variations and are generally lower than those from other on- and off-craton lithotectonic units. Nevertheless, the water contents of mineral and whole-rock in Junan peridotite xenoliths, which sourced from the juvenile lithospheric mantle, are generally higher than those elsewhere in eastern China. This suggests that the initial water content of juvenile lithospheric mantle is not low. There is no obvious correlation between the water contents and Mg^# values of minerals in the mantle xenoliths and no occurrence of diffusion profile in pyroxene, suggesting no relationship between the low water content of mantle xenolith and the diffusion loss of water during xenolith ascent with host basaltic magmas. If the subcontinental lithospheric mantle (SCLM) base is heated by the asthenospheric mantle, the diffusion loss of water is expected to occur. On the other hand, extraction of basaltic melts from the SCLM is a more efficient mechanism to reduce the water content of xenoliths. The primary melts of Mesozoic and Cenozoic basalts in eastern China have water contents, as calculated from the water contents of phenocrysts, higher than those of normal mid-ocean ridge basalts (MORB). The Mesozoic basalts exhibit similar water contents to those of island arc basalts, whereas the Cenozoic basalts exhibit comparable water contents to oceanic island basalts and backarc basin basalts with some of them resembling island arc basalts. These observations suggest the water enrichment in the mantle source of continental basalts due to metasomatism by aqueous fluids and hydrous melts derived from dehydration and melting of deeply subducted crust. Mantle-derived megacrysts, minerals in xenoliths and phenocrysts in basalts from eastern China also exhibit largely variable hydrogen isotope compositions, indicating a large isotopic heterogeneity for the Cenozoic SCLM in eastern China. The water content that is higher than that of depleted MORB mantle and the hydrogen isotope composition that is deviated from that of depleted MORB mantle suggest that the Cenozoic continental lithospheric mantle suffered the metasomatism by hydrous melts derived from partial melting of the subducted Pacific slab below eastern China continent. The metasomatism would lead to the increase of water content in the SCLM base and then to the decrease of its viscosity. As a consequence, the SCLM base would be weakened and thus susceptible to tectonic erosion and delamination. As such, the crust-mantle interaction in oceanic subduction channel is the major cause for thinning of the craton lithosphere in North China.     

Noble gas systematics for coexisting glass and olivine crystals in basalts and dunite xenoliths from Loihi Seamount

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 (R_A), 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 R_A) 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.     

New constraints on the HIMU mantle from neon and helium isotopic compositions of basalts from the Cook–Austral Islands

High ⁴He/³He ratios of 100 000 to 160 000 found at HIMU ocean islands (“high μ,” where μ is the U/Pb ratio) are usually attributed to the presence of recycled oceanic crust in the HIMU mantle source. However, significantly higher ⁴He/³He ratios are expected in recycled crust after residence in the mantle for periods greater than 1 Ga. In order to better understand the helium isotopic signatures in HIMU basalts, we have measured helium and neon isotopic compositions in a suite of geochemically well-characterized basalts from the Cook–Austral Islands. We observe ⁴He/³He ratios ranging from 56 000 to 141 000, suggesting the involvement of mantle reservoirs both more and less radiogenic than the mantle source for mid-ocean ridge basalts (MORBs). In addition, we find that the neon isotopic compositions of HIMU lavas extend from the MORB range to compositions less nucleogenic than MORBs. The Cook-Austral HIMU He–Ne isotopic compositions, along with Sr, Nd, Pb, and Os isotopic compositions, indicate that in addition to recycled crust, a relatively undegassed mantle end-member (e.g., FOZO) is involved in the genesis of these basalts. The association of relatively undegassed mantle material with recycled crust provides an explanation for the close geographical association between HIMU lavas and EM (enriched mantle)-type lavas from this island chain: EM-type signatures represent a higher mixing proportion of relatively undegassed mantle material. Mixing between recycled material and relatively undegassed mantle material may be a natural result of entrainment processes and convective stirring in deep mantle.     

Primordial neon,helium, and hydrogen in oceanic basalts

A primordial neon component in neon from Kilauea Volcano and deep-sea tholeiite glass has been identified by the presence of excess²⁰Ne; relative to atmospheric neon the²⁰Ne enrichments are 5.4% in Kilauea neon and about 2.5% in the basalts. The²⁰Ne anomalies are associated with high³He/⁴He ratios; the ratio in Kilauea helium is 15 times the atmospheric ratio, while mid-ocean ridge basalts from the Atlantic, Pacific, and Red Sea have uniform ratios about 10 times atmospheric. Mantle neon and helium are quite different in isotopic composition from crustal gases, which are highly enriched in radiogenic²¹Ne and⁴He. The²¹Ne/⁴He ratios in crustal gases are consistent with calculated values based on G. Wetherill's¹⁸O (α,n) reaction; the lack of²⁰Ne enrichment in these gases shows that the mantle²⁰Ne anomalies are not radiogenic.²¹Ne enrichments in Kilauea neon and “high-³He” Pacific tholeiites are much less than in crustal neon, about 2 ± 2% vs. present atmospheric neon, as expected from the much lower⁴He/Ne ratios.Neon concentrations in two Atlantic tholeiites were found to be only 1–2% of the values obtained by Dymond and Hogan; helium concentrations are slightly greater and our He/Ne ratios are greater by a factor of 150. The large Ne excess relative to solar wind and meteoritic gases is thus not confirmed. Pacific and Atlantic basalts appear to be quite different in He/Ne ratios however, and He and Ne may be inversely correlated. He concentration variations due to diffusive loss can be distinguished from variations due to two-phase partitioning or mantle heterogeneity by the effects on³He/⁴He ratios. The He isotopic and concentration measurements on “low-³He” basalts are consistent with diffusive loss and dilution of the 3/4 ratio by in-situ radiogenic⁴He, and may provide a method for dating basalt glasses.Deuterium/hydrogen ratios in Atlantic and Pacific tholeiite glasses are 77% lower than the ratio in seawater. The inverse correlation between deuterium and water content observed by Friedman in erupting Kilauea basalts is consistent with a Rayleigh separation process in which magmatic water is separated from an initial melt with the same D/H ratio as observed in deep-sea tholeiites. The consistency of the D/H ratios in tholeiites containing primordial He and Ne components indicates that these ratios are probably characteristic of primordial or juvenile hydrogen in the mantle.     

Helium and argon isotopes of the Tertiary basic igneous rocks from Shandong Peninsula and implications for the magma origin

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.     

Contributions of slab fluid and sediment melt components to magmatism in the Mariana Arc–Trough system: Evidence from geochemical compositions and Sr,Nd, and noble gas isotope systematics

This study presents new major and trace element, mineral, and Sr, Nd, and noble gas isotope geochemical analyses of basalts, gabbro, and clinopyroxenite from the Mariana Arc (Central Islands and Southern Seamount provinces) including the forearc, and the Mariana Trough (Central Graben and Spreading Ridge). Mantle source compositions beneath the Mariana Arc and the Mariana Trough indicate a mantle source that is depleted in high field strength elements relative to MORB (mid‐oceanic ridge basalt). Samples from the Mariana Arc, characterized by high ratios of Ba/Th, U/Th, ⁸⁴Kr/⁴He and ¹³²Xe/⁴He, are explained by addition of fluid from the subducted slab to the mantle wedge. Correlations of noble gas data, as well as large ion lithophile elements, indicate that heavy noble gases (Ar, Kr, and Xe) provide evidence for fluid fluxing into the mantle wedge. On the other hand, major elements and Sr, Nd, He, and Ne isotopic data of basalts from the Mariana Trough are geochemically indistinguishable from MORB. Correlations of ³He/⁴He and ⁴⁰Ar/³⁶Ar in the Mariana Trough samples are explained by mixing between MORB and atmosphere. One sample from the Central Graben indicates extreme enrichment in ²⁰Ne/²²Ne and ²¹Ne/²²Ne, suggesting incorporation of solar‐type Ne in the magma source. Excess ¹²⁹Xe is also observed in this sample suggesting primordial noble gases in the mantle source. The Mariana Trough basalts indicate that both fluid and sediment components contributed to the basalts, with slab‐derived fluids dominating beneath the Spreading Ridge, and that sediment melts, characterized by high La/Sm and relatively low U/Th and Zr/Nb, dominate in the source region of basalts from the Central Graben.     

Helium and neon isotopic compositions in the ophiolites from the Yarlung Zangbo River,Southwestern China:The information from deep mantle

The ophiolites from the Yarlung Zangbo River (Tibet),Southwestern China,were analysed for the con-tents of helium and neon and their isotopic compositions by stepwise heating. The serpentinites from Bainang showed a high 3He/4He value of 32.66Ra (Ra is referred to the 3He/4He ratio in the present air) in 700 ℃ fraction. At lower temperature,all of the dolerites displayed as very high 3He/4He ratios as ones investigated for hotspots. It was clear that the high 3He/4He ratio was one of immanent characterics in the magma source formed the dolerites,suggesting that there was a large amount of deep mantle fluids in these rocks. In the three-isotope diagram of neon,the data points from the ophiolites of the Yarlung Zangbo River were arranged along the Loihi Line. This is in agreement with the characteristics of he-lium isotopes,revealing that the high-3He plume from deep mantle had played an important role in the formation of the Neo-Tethyan Ocean. The helium isotopic compositions in the basalts were far higher than atomospheric value but lower than the average value of MORB,although there were various de-grees of alteration. The possible reasons were that basaltic magmas     

Nd and Sr isotope ratios and rare earth element abundances in Reykjanes Peninsula basalts evidence for mantle heterogeneity beneath Iceland

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.     

Nd and Sr isotope geochemistry of hydrous mantle nodules and their host alkali basalts: implications for local heterogeneities in metasomatically veined mantle

Nd and Sr isotopic data on pargasite Iherzolite inclusions, kaersutite megacrysts and their host alkali basalts are presented here to clarify some questions regarding isotopic equilibration during mantle metasomatism and the role of metasomatism in basalt genesis. Five alkali basalts from Nunivak Island within the Aleutian back-arc basin, have⁸⁷Sr/⁸⁶Sr ratios of 0.70251–0.70330 and¹⁴³Nd/¹⁴⁴Nd ratios of 0.51289–0.51304. On a Nd versus Sr isotope composition diagram the basalts overlap the fields of MORB and ocean island basalts. Pargasites and mica separated from hydrous nodules found in these basalts have a range in⁸⁷Sr/⁸⁶Sr of 0.70256–0.70337 but identical¹⁴³Nd/¹⁴⁴Nd ratios of 0.51302. The metasomatic fluid represented by the pargasite is in isotopic equilibrium, both for Sr and Nd, with the dry mantle as represented by diopside. Eight alkali basalts from the Ataq diatreme, South Yemen, have⁸⁷Sr/⁸⁶Sr range of 0.70335–0.70426 and¹⁴³Nd/¹⁴⁴Nd range of 0.51252–0.51305. On a Nd versus Sr isotope composition diagram the basalts from Ataq plot in two distinct fields, (1) within the field of ocean island basalts, and (2) within the range of continental rift basalts but to the left of the Nd-Sr correlation line, somewhat similar to the Skye and Oslo rift basalts. Diopside and pargasite separated from three nodules at Ataq have a more complex history than those at Nunivak. Two nodules contain pargasite and diopside with identical⁸⁷Sr/⁸⁶Sr ratios but different¹⁴³Nd/¹⁴⁴Nd ratios. A third nodule contains diopside with a¹⁴³Nd/¹⁴⁴Nd ratio similar to that of other diopsides.The Nunivak basalts are derived from a source with a time-integrated light-REE depletion, in contrast to the light-REE-enriched nature of the basanites. This is best explained by a recent metasomatic event in the source region which increased the LIL element content of the peridotite thus accommodating higher degrees of melting. The Ataq volcanic rocks seem to tap different sources characterized by both light-REE enrichment and depletion, in contrast to the uniform source of the Nunivak basanites. Production of the Ataq basanites is believed to involve anataxis of metasomatically veined continental mantle where local mantle heterogeneities survived the melting event.     

Hydrogen diffusion in clinopyroxene: dehydration experiments

Hydrogen diffusivity of one clinopyroxene megacryst from Nüshan, eastern China parallel to [001]* crystallographic direction was measured by high-temperature sequential dehydration experiments at 950℃ and 850℃, which was (6.5± 1.5)×10-12(m2/s) and (1.8± 0.7)×10-12(m2/s) respectively. From these results and the previous published data, it seems that the correlation between hydrogen diffusivity and Fe content suggested by Dyar et al. (1996) possibly does not exist. Clinopyroxene megacrysts from alkali basalts appear to be possible reliable samples for the study of the water evolution and hydrogen isotope compositions of the upper mantle.     

Excess 3He in oceanic basalts: Evidence for terrestrial primordial helium

Helium trapped in the chilled glass rims of Pacific Ocean basalts is highly enriched in ³He; the ³He/⁴He and ³He/Ne ratios are respectively 10 and 1000 times the atmospheric ratios. We interpret these large enrichments as further evidence that primordial ³He is still present in the interior of the earth. The ³He/⁴He ratio in basalt glass is the same as the isotope ratio of the “excess helium” in Pacific Ocean deep water, supporting the theory that the atmospheric escape rate of ³He is balanced by a flux of primordial ³He from the mantle.     

Primitive neon and helium isotopic compositions of high-MgO basalts from the Kerguelen Archipelago,Indian Ocean

The geochemical characteristics of mildly alkalic basalts (24–25 Ma) erupted in the southeastern Kerguelen Archipelago are considered to represent the best estimate for the composition of the enriched Kerguelen plume end-member. A recent study of picrites and high-MgO basalts from this part of the archipelago highlighted the Pb and Hf isotopic variations and suggested the presence of mantle heterogeneities within the Kerguelen plume itself. We present new helium and neon isotopic compositions for olivines from these picrites and high-MgO basalts (6–17 wt.% MgO) both to constrain the enriched composition of the Kerguelen plume and to determine the origin of isotopic heterogeneities involved in the genesis of Kerguelen plume-related basalts. The olivine phenocrysts have extremely variable ⁴He / ³He compositions between MORB and primitive values observed in OIB (∼90,000 to 40,000; i.e., R / R_a ∼8 to 18) and they show primitive neon isotopic ratios (average ²¹Ne / ²¹Ne_ext ∼0.044). The neon isotopic systematics and the ⁴He / ³He ratios that are lower than MORB values for the Kerguelen basalts clearly suggest that the Kerguelen hotspot belongs to the family of primitive hotspots, such as Iceland and Hawaii. The rare gas signature for the Kerguelen samples, intermediate between MORB and solar, is apparently inconsistent with mixing of a primitive component with a MORB-like source, but may result from sampling a heterogeneous part of the mantle with solar ³He / ²²Ne and with a higher (U, Th) / ³He ratio compared to typically high R / R_a hotspot basalts such as those from Iceland and Hawaii.     

Helium isotopic variations in volcanic rocks from Loihi Seamount and the Island of Hawaii

Helium isotopic ratios ranging from 20 to 32 times the atmospheric ³He/⁴He(R_A) have been observed in a suite of 15 basaltic glasses from the Loihi Seamount. These ratios, which are up to four times higher than those of MORB glasses and more than twice those of nearby Kilauea, are strongly suggestive of a primitive source of volatiles supplying this volcanism. The Loihi glasses measured span a broad compositional range, and the ³He/⁴He ratios were found to be generally lower for the alkali basalts than for the tholeiites. The component with a lower ³He/⁴He ratio appears to be associated with olivine xenocrysts, within which fluid inclusions are probably the carrier of contaminant helium. One Loihi sample has a much lower isotopic ratio (<5 R_A), but a combination of low He concentration, high vesicularity, and presence of cracks lined with clay minerals suggests that the low ratio is due to gas loss and contamination by atmospheric helium.Crushing and melting experiments show that for modest vesicularities (<5% by volume) the Loihi glasses obey a MORB-type partitioning trend, but at higher vesicularities the data show considerably more scatter due to volatile mobilization. The high vesicularities, low extrusion pressure and generally low helium concentrations are consistent with a considerable degree of degassing. Analyses of dunites, plus a correlation between total helium concentrations with xenocryst abundances also suggest that xenocrysts are a significant carrier of contaminating (low ³He/⁴He) helium.³He/⁴He ratios from samples of other Hawaiian volcanoes (Kilauea, Mauna Loa, Hualalai, and Mauna Kea) show a smooth decrease in ³He/⁴He with increasing volcano age and volume. We interpret this to be a synoptic picture of the time evolution of a hot-spot diapir: the earliest stage is characterized by primitive (> 30 R_A) helium with some (variable) component of lithospheric contamination added during “breakthrough”, while the later stages are characterized by a relaxation toward lithospheric ³He/⁴He ratios (～ 8 R_A) due to isolation of the diapir from the mantle below (as the plate moves on), and subsequent mining of the inherited helium and contamination from the surrounding lithosphere. The abrupt contrast in ³He/⁴He ratios between Kilauea and Loihi, despite their close proximity, is indicative of the small lateral extent of the plume.     

Chemical heterogeneity of the Archaean mantle,composition of the earth and mantle evolution

New rare earth element (REE) data for Archaean basalts and spinifex-textured peridotites (STP) show a range of La/Sm ratios (chondrite-normalized) from 0.36 to 3.5, with the bulk of the data in the range 0.7–1.3. This supports the hypothesis, based on Sr isotope initial ratios, that the Archaean mantle was chemically heterogeneous. We suggest that the bulk mantle source for Archaean basaltic magmas was close to an undepleted earth material. An average chemical composition of the Archaean mantle is estimated using chemical regularities observed in Archaean STP and high-magnesian basalts. TiO₂ and MgO data show an inverse correlation which intersects the MgO axis at about 50% MgO (Fo₉₂). TiO₂ abundance in the mantle source is measured on this plot by assigning anMgO= 38% for the mantle. Concentrations of other elements are also estimated and these data are then used to obtain a composition for the bulk earth. We suggest an earth model with about 1.35 times ordinary chondrite abundances of refractory lithophile elements and about 0.2 times carbonaceous type 1 chondrite abundances of moderately volatile elements (such as Na, Rb, K, Mn). P shows severe depletion in the model earth relative to carbonaceous chondrites, a feature either due to volatilization or core formation (preferred). Our data support the hypothesis of Ringwood that the source material for the earth is a carbonaceous chondrite-like material.The generation of mid-ocean ridge basalts (MORB) is examined in the light of the model earth composition and Al₂O₃/TiO₂, CaO/TiO₂ ratios. It is suggested that for primitive basalts, these values can be used to predict the residual phases in their source. Comparison of chemical characteristics of inferred sources for 2.7-b.y. Archaean basalts and modern “normal” MORB indicates that the MORB source is severely depleted in highly incompatible elements such as Cs, Ba, Rb, U, Th, K, La and Nb, but has comparable abundances of less incompatible elements such as Ti, Zr, Y, Yb. The cause of the depletion in the MORB source is examined in terms of crust formation and extraction of silica-undersaturated melts. The latter seems to be a more likely explanation, since the degree of enrichment of highly incompatible elements in the crust only accounts for up to 40% of their abundances in the bulk earth and cannot match the depletion pattern in normal MORB. A large volume of material, less depleted than the source for normal MORB must therefore exist in the mantle and can serve as the source for the ocean island basalts and “normal” MORB.Three different mantle evolution models are examined and each suggests that the mantle is stratified with respect to abundances of incompatible trace elements. We suggest that no satisfactory model is available to fully explain the spectrum of geochemical and geophysical data. In particular the Pb and Sr isotope data on oceanic basalts, the depletion patterns of MORB and the balance between lithophile abundances in the crust and mantle, are important geochemical constraints to mantle models. Further modelling of the mantle evolution will be dependent on firmer information on the role of subduction, mantle convection pattern, and basalt production through geologic time together with a better understanding of the nature of Archaean crustal genesis.     

Gold contents of both mantle-derived xenoliths and sulfides in them from eastern China

The gold contents of 59 samples of mantle-derived xenoliths, along with 85 samples of sulfide assem-blages in them, of Cenozoic basalt from eight districts in eastern China are analyzed. The gold contents of mantle xenoliths usually fall in the range of 10-9―10-8, whereas those of the sulfide assemblages fall in the range of 10-4―10-2. This implies that the latter are several hundred thousand times higher than the former, and thus that Au in the mantle is concentrated mostly in sulfide assemblages. Gold con-tents of both mantle-derived xenoliths and sulfide assemblages in them are inhomogeneous spatially, but their distribution rules are similar. Except the samples from Hainan Province, either the mantle xenoliths with high gold content or sulfide assemblages of the mantle-derived xenoliths with high gold content are distributed mostly on the north and south margins of the North China platform (Hannuoba of Hebei Province and Linqu, Changle of Shandong Province), corresponding to districts with concen-trated gold deposits in northwest Hebei Province and Jiaodong Peninsula of Shandong Province. This may reflect the correlativity in age, nature and composition between the continental crust and the un-derlying lithospheric mantle. The underlying lithospheric mantle of the North China platform is an an-cient gold-rich lithospheric mantle. The gold-rich lithospheric mantle may be the material source of later activation, enrichment, transportation and mineralization of gold by auriferous CO2 mantle fluids.     

Refining the noble gas record of the Réunion mantle plume source: Implications on mantle geochemistry

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.     

Characteristics and origins of primary fluids and noble gases in mantle-derived minerals from the Yishu area, Shandong Province, China

springerlink.com Studies of mantle fluids are currently one of the hot topics in the earth science, greatly contributing to re-vealing origins and evolutions of fluids. In general, the concept of mantle fluids refers to their active compo-nents, such as CO2, H2O, N2, etc., while the noble gases inert in chemical properties belong to another research system. Due to their marked differences in various fluid sources of the Earth[1], the isotopic sig-natures of He and Ar have been widely used a…     

Helium isotopes in the earth's interior and in the atmosphere: A degassing model of the earth

A first-order degassing model was applied to describe the evolution of helium content and isotope composition in the earth and in the atmosphere. The main events described by the model are: (1) the earth-trapped primordial rare gases at the moment of its accretion; (2) later, the solid earth lost primordial and radiogenic rare gases, and (3) they were accumulated in the atmosphere; (4) in addition,³He was formed in the atmosphere due to cosmic irradiation, accretion from solar wind, etc.; (5)³He and⁴He dissipated into space at different loss rates.Study of this model confirms the concept that some of primordial helium is retained in the interior of the earth; terrestrial helium (³He/⁴He～ 2 × 10^?5) was most probably formed as a mixture of primordial (³He/⁴He= 3 × 10^?4) and radiogenic (³He/⁴He～ 3 × 10^?8) helium. For achondritic concentrations of heavy radioactive elements (U= 2.25 × 10^?8g/g) the calculated⁴He flux from the earth is equal to 5.7 × 10⁶ at cm^?2 sec^?1. The corresponding³He flux is about 114 at cm^?2 sec^?1. In discussing the aeronomic problem of helium it is necessary to take into account that the earth is the main source of the light helium isotope.     

Major and trace element and Sr–Nd isotope signatures of lavas from the Central Lau Basin: Implications for the nature and influence of subduction components in the back-arc mantle

New major and trace element and Sr–Nd isotope data are presented for basaltic glasses from active spreading centers (Central Lau Spreading Center (CLSC), Relay Zone (RZ) and Eastern Lau Spreading Center (ELSC)) in the Central Lau Basin, SW Pacific. Basaltic lavas from the Central Lau Basin are mainly tholeiitic and are broadly similar in composition to mid-ocean ridge basalts (MORB). Their generally high ⁸⁷Sr/⁸⁶Sr ratios, combined with relatively low ¹⁴³Nd/¹⁴⁴Nd ratios are more akin to MORB from the Indian rather than Pacific Ocean. In detail, the CLSC, RZ and ELSC lavas are generally more enriched in large ion lithophile elements (Rb, Ba, Sr, and K) than average normal-MORB, which suggests that the mantle beneath the Central Lau Basin was modified by subducted slab-derived components. Fluid mobile/immobile trace element and Sr – Nd isotope ratios suggest that the subduction components were essentially transferred into the mantle via hydrous fluids derived from the subducted oceanic crust; contributions coming from the subducted sediments are minor. Compared to CLSC lavas, ELSC and RZ lavas show greater enrichment in fluid mobile elements and depletion in high field strength elements, especially Nb. Thus, with increasing distance away from the arc, the influence of subduction components in the mantle source of Lau Basin lavas diminishes. The amount of hydrous fluids also influences the degree of partial melting of the mantle beneath the Central Lau Basin, and hence the degree of melting also decreases with increasing distance from the arc.