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1.
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 / Ra ∼8 to 18) and they show primitive neon isotopic ratios (average 21Ne / 21Neext ∼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 / Ra hotspot basalts such as those from Iceland and Hawaii.  相似文献   

2.
SHRIMP zircon U–Pb dating, mineral chemical, element geochemical and Sr–Nd–Pb–Hf isotopic data have been determined for the Yulong monzogranite-porphyry in the eastern Tibet, China. The Yulong porphyry was emplaced into Triassic strata at about 39 Ma. The rocks are weakly peraluminous and show shoshonitic affinity, i.e., alkalis-rich, high K2O contents with high K2O / Na2O ratios, enrichment in LREE and LILE. They also show some affinities with the adakite, e.g., high SiO2 and Al2O3, and low MgO contents, depleted in Y and Yb, and enrichment in Sr with high Sr / Y and La / Yb ratios, and no Eu anomalies. The Yulong porphyry has radiogenic 87Sr / 86Sr (0.7063–0.7070) and unradiogenic 143Nd / 144Nd (εNd = − 2.0 to − 3.0) ratios. The Pb isotopic compositions of feldspar phenocrysts separated from the Yulong porphyry show a narrow range of 206Pb / 204Pb ratios (18.71–18.82) and unusually radiogenic 207Pb / 204Pb (15.65–15.67) and 208Pb / 204Pb (38.87–39.00) ratios. In situ Hf isotopic composition of zircons that have been SHRIMP U–Pb dated is characterized by clearly positive initial εHf values, ranging from + 3.1 to + 5.9, most between + 4 and + 5. Phenocryst clinopyroxene geothermometry of the Yulong porphyry indicates that the primary magmas had anomalously high temperature (> 1200 °C). The source depth for the Yulong porphyry is at least 100 km inferred by the metasomatic volatile phase (phlogopite–carbonate) relations. Detailed geochemical and Sr–Nd–Pb–Hf isotopic compositions not only rule out fractional crystallization or assimilation-fractional crystallization processes, but also deny the possibility of partial melting of subducted oceanic crust or basaltic lower crust. Instead, low degree (1–5%) partial melting of a metasomatized lithosphere (phlogopite–garnet clinopyroxenite) is compatible with the data. This example gives a case study that granite can be derived directly by partial melting of an enriched lithospheric mantle, which is important to understand the source and origin of diverse granites.  相似文献   

3.
New trace element and Hf, Nd, and Pb isotope data are reported for 22 basalts collected between 22°N and 35°N on the Mid-Atlantic Ridge. (La / Sm)N ratios identify the presence of enriched (E)-MORB in the northernmost part of this area and normal (N)-MORB elsewhere. A negative correlation is observed when 143Nd / 144Nd is plotted against 206Pb / 204Pb, 207Pb / 204Pb, and 208Pb / 204Pb, whereas 176Hf / 177Hf appears not to correlate with any of the other isotopic ratios. The E-MORB samples are characterized by high 206Pb / 204Pb, 207Pb / 204Pb, 208Pb / 204Pb, and low 143Nd / 144Nd. Principal Component Analysis (PCA) of Pb isotopes alone identifies three, and only three, significant geochemical end-members (‘components’). Including Nd and Hf isotopic data in the PCA produces spurious components, partly because of curved mixing relationships, and partly because of fractionation during melting. Our preferred interpretation of why 176Hf / 177Hf is decoupled from the other isotopic ratios is, as inferred from recent experimental data, that the Hf isotopic compositions of the melt and the residue fail to equilibrate during melting. A strong correlation between (Sr / Nd)N and (Eu / Eu*)N indicates that plagioclase is a residual phase of N-MORB, but not of E-MORB melting. The three end-members identified in this study are the depleted mantle, a common-type component, and an enriched plume-type end-member. The common, or ‘C’-type, end-member is characteristic of E-MORB and may itself be a mixture containing recycled oceanic crust (the MORB suite, terrigenous sediments, and/or oceanic plateaus). The plume-type end-member is likely to represent the lower mantle and may involve some primordial material. It is shown that mantle isochrons in general and the Pb–Pb isochron in particular do not characterize a specific geodynamic process acting to create mantle heterogeneities.  相似文献   

4.
Kutch (northwest India) experienced lithospheric thinning due to rifting and tholeiitic and alkalic volcanism related to the Deccan Traps K/T boundary event. Alkalic lavas, containing mantle xenoliths, form plug-like bodies that are aligned along broadly east–west rift faults. The mantle xenoliths are dominantly spinel wehrlite with fewer spinel lherzolite. Wehrlites are inferred to have formed by reaction between transient carbonatite melts and lherzolite forming the lithosphere. The alkalic lavas are primitive (Mg# = 64–72) relative to the tholeiites (Mg# = 38–54), and are enriched in incompatible trace elements. Isotope and trace element compositions of the tholeiites are similar to what are believed to be the crustally contaminated Deccan tholeiites from elsewhere in India. In terms of Hf, Nd, Sr, and Pb isotope ratios, all except two alkalic basalts plot in a tight cluster that largely overlap the Indian Ridge basalts and only slightly overlap the field of Reunion lavas. This suggests that the alkalic magmas came largely from the asthenosphere mixed with Reunion-like source that welled up beneath the rifted lithosphere. The two alkalic outliers have an affinity toward Group I kimberlites and may have come from an old enriched (metasomatized) asthenosphere. We present a new model for the metasomatism and rifting of the Kutch lithosphere, and magma generation from a CO2-rich lherzolite mantle. In this model the earliest melts are carbonatite, which locally metasomatized the lithosphere. Further partial melting of CO2-rich lherzolite at about 2–2.5 GPa from a mixed source of asthenosphere and Reunion-like plume material produced the alkalic melts. Such melts ascended along deep lithospheric rift faults, while devolatilizing and exploding their way up through the lithosphere. Tholeiites may have been generated from the main plume head further south of Kutch.  相似文献   

5.
Os–Hf–Sr–Nd isotopes and PGE were determined in peridotite xenoliths carried to the surface by Quaternary alkali basaltic magmas in the Tokinsky Stanovik Range on the Aldan shield. These data constrain the timing and nature of partial melting and metasomatism in the lithospheric mantle beneath SE Siberian craton. The xenoliths range from the rare fertile spinel lherzolites to the more abundant, strongly metasomatised olivine-rich (70–84%) rocks. Hf–Sr–Nd isotope compositions of the xenoliths are mainly within the fields of oceanic basalts. Most metasomatised xenoliths have lower 143Nd / 144Nd and 176Hf / 177Hf and higher 87Sr / 86Sr than the host basalts indicating that the metasomatism is older and has distinct sources. A few xenoliths have elevated 176Hf / 177Hf (up to 0.2838) and plot above the Hf–Nd mantle array defined by oceanic basalts.187Os / 188Os in the poorly metasomatised, fertile to moderately refractory (Al2O3 ≥ 1.6%) Tok peridotites range from 0.1156 to 0.1282, with oldest rhenium depletion ages being about 2 Ga. The 187Os / 188Os in these rocks show good correlations with partial melting indices (e.g. Al2O3, modal cpx); the intercept of the Al–187Os / 188Os correlation with lowest Al2O3 estimates for melting residues (∼0.3–0.5%) has a 187Os / 188Os of ∼0.109 suggesting that these peridotites may have experienced melt extraction as early as 2.8 Gy ago. 187Os / 188Os in the strongly metasomatised, olivine-rich xenoliths (0.6–1.3% Al2O3) ranges from 0.1164 to 0.1275 and shows no apparent links to modal or chemical compositions. Convex-upward REE patterns and high abundances of heavy to middle REE in these refractory rocks indicate equilibration with evolved silicate melts at high melt / rock ratios, which may have also variably elevated their 187Os / 188Os. This inference is supported by enrichments in Pd and Pt on chondrite-normalised PGE abundance patterns in some of the rocks. The melt extraction ages for the Tok suite of 2.0 to 2.8 Ga are younger than oldest Os ages reported for central Siberian craton, but they must be considered minimum estimates because of the extensive metasomatism of the most refractory Tok peridotites. This metasomatism could have occurred in the late Mesozoic to early Cenozoic when the Tok region was close to the subduction-related Pacific margin of Siberia and experienced large-scale tectonic and magmatic activity. This study indicates that metasomatic effects on the Re–Os system in the shallow lithospheric mantle can be dramatic.  相似文献   

6.
Late Cretaceous (66.2 ± 0.5 Ma amphibole and 66.7 ± 0.2 Ma phlogopite 40Ar/39Ar ages) nephelinitic volcanic rocks from Godzilla Seamount in the eastern North Atlantic (34°N latitude) have trace element and Sr–Nd–Pb–Hf-isotope compositions similar to the Enriched Mantle I (EM-I) endmember, except for their low 207Pb/204Pb relative to 206Pb/204Pb ratios (206Pb/204Pbin = 17.7, 207Pb/204Pbin = 15.34) plotting below the Northern Hemisphere Reference Line on the uranogenic Pb isotope diagram. O isotope data on amphibole separates are mantle-like (δ18O = 5.6–5.8‰). Age and location of the isolated Godzilla Seamount, however, preclude it from being derived from the Madeira or Canary hotspots, making a lower-mantle origin unlikely. Therefore we propose derivation from a shallow (lithospheric/asthenospheric) melting anomaly. As observed in mid-ocean-ridge and ocean-island basalts, there is a systematic decrease of 207Pb/204Pb ratios (and Δ7/4) in the individual EM-I endmember type localities towards northern latitudes with Godzilla lying on the extension of this trend. This trend is mirrored in ultra-potassic volcanic rocks such as lamproites and kimberlites, which reflect the composition of enriched subcontinental lithospheric mantle. Therefore, a global pattern in 207Pb/204Pb ratios and Δ7/4 is suggested. The geochemical composition of EM-I endmember type localities, including Godzilla lavas, and the enriched (DUPAL) anomaly in the southern hemisphere could reflect derivation from ancient, metasomatized subcontinental lithospheric mantle. We propose a two-stage model to explain the trace element and isotopic composition of the EM-I mantle endmember localities worldwide: 1) during the early history of the Earth, subcontinental lithosphere was metasomatized by melts from subducted slabs along convergent margins generating high μ (238U/204Pb) sources, and 2) as the Earth cooled, hydrous fluids replaced hydrous melts as the main slab component metasomatizing the subcontinental lithospheric mantle (generating EM-I sources with lower μ). In accordance with this model, the global variations in 207Pb/204Pb ratios and Δ7/4 could reflect geographic differences in μ and/or the age at which the transition from stages 1 to 2 took place in the Archaean lithosphere. The model would require a re-definition of the EM-I endmember to low 206Pb/204Pb, high 208Pb/204Pb (positive Δ8/4) but variable 207Pb/204Pb (positive and negative Δ7/4).  相似文献   

7.
In order to better understand the nature and formation of oceanic lithosphere beneath the Early Cretaceous Ontong Java Plateau, Re–Os isotopes have been analysed in a suite of peridotite xenoliths from Malaita, Solomon Islands. Geological, thermobarometric and petrological evidence from previous studies reveal that the xenoliths represent virtually the entire thickness of the southern part of subplateau lithospheric mantle (< 120 km). This study demonstrates that vertical Os isotopic variations correlate with compositional variations in a stratified lithosphere. The shallowest plateau lithosphere (< 85 km) is dominated by fertile lherzolites showing a restricted range of 187Os/188Os (0.1222 to 0.1288), consistent with an origin from ~ 160 Ma Pacific lithosphere. In contrast, the basal section of subplateau lithospheric mantle (~ 95–120 km) is enriched in refractory harzburgites with highly unradiogenic 187Os/188Os ratios ranging from 0.1152 to 0.1196, which yield Proterozoic model ages of 0.9–1.7 Ga. Although the whole range of Os isotope compositions of Malaita peridotites is within the variations seen in modern abyssal peridotites, the contrasting isotopic compositions of shallow and deep plateau lithosphere suggest their derivation from different mantle reservoirs. We propose that the subplateau lithosphere forms a genetically unrelated two-layered structure, comprising shallower, typical oceanic lithosphere underpinned by deeper impinged material, which included a component of recycled Proterozoic lithosphere. The impingement of residual but chemically heterogeneous mantle, mechanically coupled to the recently formed, thin lithosphere, may have a bearing on the anomalous initial uplift and late subsidence history of the seismically anomalous plateau root.  相似文献   

8.
We report volatile (H2O, CO2, F, S, Cl) and trace element data for submarine alkalic basalt glasses from the three youngest Samoan volcanoes, Ta'u, Malumalu and Vailulu'u. Most samples are visibly sulfide saturated, so have likely lost some S during fractionation. Cl / K ratios (0.04–0.15) extend to higher values than pristine MORBs, but are suspected to be partly due to source differences since Cl / K roughly varies as a function of 87Sr / 86Sr. There are no resolvable differences in the relative enrichment of F among sources, and compatibility of F during mantle melting is established to be nearly identical to Nd. Shallow degassing has affected CO2 in all samples, and H2O only in the most shallowly erupted samples from Vailulu'u. Absolute water contents are high for Samoa (0.63–1.50 wt.%), but relative enrichment of water compared to equally incompatible trace elements (Ce, La) is low and falls entirely below normal MORB values. H2O / Ce (58–157) and H2O / La (120–350) correlate inversely with 87Sr / 86Sr compositions (0.7045–0.7089). This leads us to believe that, because of very fast diffusion of hydrogen in mantle minerals, recycled lithospheric material with high initial water and trace element content will lose water to the drier ambient mantle during storage within the inner Earth. The net result is the counter-intuitive appearance of greater dehydration with greater mantle enrichment. We expect that subducted slabs will experience a two-stage dehydration history, first within subduction zones and then in the ambient mantle during long-term convective mixing.  相似文献   

9.
Abundant dunite and harzbugite xenoliths are preserved in Early Cretaceous high-Mg# [63–67, where Mg# = molar 100 × Mg/(Mg + Fetot)] diorite intrusions from western Shandong in the North China Craton (NCC). Dunite and some harzburgite xenoliths typically preserve areas of orthopyroxenite (sometimes accompanied by phlogopite) either as veins or as zones surrounding chromite grains. Harzburgite is chiefly composed of olivine, orthopyroxene, minor clinopyroxene and chromian-spinel. High Mg#'s (averaging 91.4) and depletions in Al2O3 and CaO (averaging 0.52 wt.% and 0.29 wt.%, respectively) in harzburgite and dunite xenoliths suggest that they are residues formed by large degrees of polybaric melting. However, olivines and orthopyroxenes from dunite xenoliths spatially associated with orthopyroxenite display lower Mg#'s (i.e., 82–87 and 83–89, respectively), suggesting that an adakitic melt–peridotite reaction has taken place. This is consistent with the production of veined orthopyroxene or orthopyroxene + phlogopite in dunite and some harzburgite xenoliths in response to the introduction of adakitic melt into the previously depleted lithospheric mantle (i.e., harzburgite and dunite xenoliths). The presence of orthopyroxene in veins or as a zones surrounding chromite in peridotite xenoliths is thought to be representative of adakitic melt metasomatism. The dunite and harzbugite xenoliths are relatively rich in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), poor in heavy rare earth elements (HREEs) and high field strength elements (HFSEs), and lack Eu anomalies on chondrite normalized trace element diagrams. The initial 87Sr/86Sr ratios and εNd(t) values for the xenoliths range from 0.7058 to 0.7212 and + 0.18 to ? 19.59, respectively. Taken together, these features, combined with the strong depletion in HFSE and the existence of Archean inherited zircons in the host rocks, suggest that the adakitic melt was derived from the partial melting of early Mesozoic delaminated lower continental crust. The interaction of the adakitic melt with peridotite is responsible for the high-Mg# character of the early Cretaceous diorites in western Shandong.  相似文献   

10.
《Continental Shelf Research》1999,19(9):1113-1141
Relationships among primary production, chlorophyll, nutrients, irradiance and mixing processes were examined along the salinity gradient in the Mississippi River outflow region. A series of six cruises were conducted during 1988–1992 at various times of year and stages of river discharge. Maximum values of biomass and primary production were typically observed at intermediate salinities and coincided with non-conservative decreases in nutrients along the salinity gradient. Highest values of productivity (>10 gC m−2 d−1) and biomass (>30 mg chlorophyll a m−3) were observed in April 1988, July–August 1990 and April–May 1992; values were lower in March and September 1991. Rates of primary production were apparently constrained by low irradiance and mixing in the more turbid, low salinity regions of the plume, and by nutrient limitation outside the plume. Highest values of primary production occurred at stations where surface nutrient concentrations exhibited large deviations from conservative mixing relationships, indicating that depletion of nutrients was related to phytoplankton uptake. Mixing and advection were important in determining the location and magnitude of primary production maxima and nutrient depletion. In addition to growth within plume surface waters, enhanced growth and/or retention of biomass may have occurred in longer residence time waters at the plume edge and/or beneath the surface plume. Vertical structure of some plume stations revealed the presence of subsurface biomass maxima in intermediate salinity water that was depleted in nutrients presumably by uptake processes. Exchange between subsurface water and the surface plume apparently contributed to the reduction in nutrients at intermediate salinities in the surface layer. DIN (=nitrate+nitrite+ammonium) : PO4 (=phosphate) ratios in river water varied seasonally, with high values in winter and spring and low values in late summer and fall. Periods of high DIN : PO4 ratios in river nutrients coincided with cruises when surface nutrient concentrations and their ratios indicated a high probability for P limitation. N limitation was more likely to occur at high salinities and during late summer and fall. Evidence for Si limitation was also found, particularly in spring.  相似文献   

11.
Miocene to Quaternary large basaltic plateaus occur in the back-arc domain of the Andean chain in Patagonia. They are thought to result from the ascent of subslab asthenospheric magmas through slab windows generated from subducted segments of the South Chile Ridge (SCR). We have investigated three volcanic centres from the Lago General Carrera–Buenos Aires area (46–47°S) located above the inferred position of the slab window corresponding to a segment subducted 6 Ma ago. (1) The Quaternary Río Murta transitional basalts display major, trace elements, and Sr and Nd isotopic features similar to those of oceanic basalts from the SCR and from the Chile Triple Junction near Taitao Peninsula (e.g., (87Sr/86Sr)o = 0.70396–0.70346 and εNd = + 5.5 − + 3.0). We consider them as derived from the melting of a Chile Ridge asthenospheric mantle source containing a weak subduction component. (2) The Plio-Quaternary (< 3.3 Ma) post-plateau basanites from Meseta del Lago Buenos Aires (MLBA), Argentina, likely derive from small degrees of melting of OIB-type mantle sources involving the subslab asthenosphere and the enriched subcontinental lithospheric mantle. (3) The main plateau basaltic volcanism in this region is represented by the 12.4–3.3-Ma-old MLBA basalts and the 8.2–4.4-Ma-old basalts from Meseta Chile Chico (MCC), Chile. Two groups can be distinguished among these main plateau basalts. The first group includes alkali basalts and trachybasalts displaying typical OIB signatures and thought to derive from predominantly asthenospheric mantle sources similar to those of the post-plateau MLBA basalts, but through slightly larger degrees of melting. The second one, although still dominantly alkalic, displays incompatible element signatures intermediate between those of OIB and arc magmas (e.g., La/Nb > 1 and TiO2 < 2 wt.%). These intermediate basalts differ from their strictly alkalic equivalents by having lower High Field Strength Element (HFSE) and higher εNd (up to + 5.4). These features are consistent with their derivation from an enriched mantle source contaminated by ca. 10% rutile-bearing restite of altered oceanic crust. The petrogenesis of the studied Mio-Pliocene basalts from MLBA and MCC is consistent with contributions of the subslab asthenosphere, the South American subcontinental lithospheric mantle and the subducted Pacific oceanic crust to their sources. However, their chronology of emplacement is not consistent with an ascent through an asthenospheric window opened as a consequence of the subduction of segment SCR-1, which entered the trench at 6 Ma. Indeed, magmatic activity was already important between 12 and 8 Ma in MLBA and MCC as well as in southernmost plateaus, i.e., 6 Ma before the subduction of the SCR-1 segment. We propose a geodynamic model in which OIB and intermediate magmas derived from deep subslab asthenospheric mantle did uprise through a tear-in-the-slab, which formed when the southernmost segments of the SCR collided with the Chile Trench around 15 Ma. During their ascent, they interacted with the Patagonian supraslab mantle and, locally, with slivers of subducted Pacific oceanic crust that contributed to the geochemical signature of the intermediate basalts.  相似文献   

12.
We use thermodynamically self-consistent and hybrid methods to analyze the correlation of important physical parameters (e.g. bulk density, elastic moduli) with bulk Mg# and modal composition in mantle peridotites at upper mantle conditions. Temperature (anharmonic and anelastic), pressure and compositional derivatives for all these parameters are evaluated. The results show that the widely used correlations between Vp/Vs and Mg# in peridotites are strictly valid only for garnet-bearing assemblages at temperatures < 900 °C. The correlation breaks down when: i) spinel is the stable Al-rich phase in the assemblage and ii) when anelastic attenuation of seismic velocities becomes important (T ? 900 °C). This implies that the range of applicability of published Vp/Vs–Mg# correlations for the upper mantle is limited to a depth interval between the spinel–garnet phase transition and the 900 °C isotherm. We use numerical simulations to show that this depth interval is virtually nonexistent in lithospheres thinner than ～ 140 km and can comprise up to ～ 50% of the lithospheric mantle in thick (> 220 km) lithospheric domains. In addition, we show that for most of the upper mantle the expected Δ(Vp/Vs) values associated with compositional variations are smaller than the resolution limit of current seismological methods. All these considerations suggest that the Vp/Vs ratio is not a reliable measure of compositional variations and that for large parts of the upper mantle compositional anomalies cannot be separated from thermal anomalies on the basis of seismological studies only. We further confirm that the only reliable indicator of compositional anomalies in a peridotitic mantle is the ratio of density to shear wave velocities (ρ/Vs). Our results demonstrate that geophysical–petrological models (forward or inverse) that model these two fields (i.e. density and Vs) self-consistently within a robust thermodynamic framework are necessary for characterizing the small-scale thermal and compositional structure of the lithosphere and sublithospheric upper mantle.  相似文献   

13.
The Earth's mantle is chemically and isotopically heterogeneous, and a component of recycled oceanic crust is generally suspected in the convecting mantle [Hofmann and White, 1982. Mantle plumes from ancient oceanic crust. Earth Planet. Sci. Lett. 57, 421–436]. Indeed, the HIMU component (high µ = 238U/204Pb), one of four isotopically distinct end-members in the Earth's mantle, is generally attributed to relatively old (≥ 1–2 Ga) recycled oceanic crust in the form of eclogite/pyroxenite, e.g. [Zindler and Hart, 1986. Chemical geodynamics. Ann. Rev. Earth Planet. Sci. 14, 493–571]. Although the presence of the recycled component is generally supported by element and isotopic data, little is known about its physical state at mantle depths. Here we show that the concentrations of Ni, Mn and Ca in olivine from the Canarian shield stage lavas, which can be used to assess the physical nature of the source material (peridotite versus olivine-free pyroxenite) [Sobolev et al., 2007. The amount of recycled crust in sources of mantle-derived melts. Science 316, 412–417], correlate strongly with bulk rock Sr, Nd and Pb isotopic ratios. The most important result following from our data is that the enriched, HIMU-type (having higher 206Pb/204Pb than generally found in the other mantle end-members) signature of the Canarian hotspot magmas was not caused by a pyroxenite/eclogite constituent of the plume but appears to have been primarily hosted by peridotite. This implies that the old (older than ~ 1 Ga) ocean crust, which has more evolved radiogenic isotope compositions, was stirred into/reacted with the mantle so that there is not significant eclogite left, whereas younger recycled oceanic crust with depleted MORB isotopic signature (< 1 Ga) can be preserved as eclogite, which when melted can generate reaction pyroxenite.  相似文献   

14.
We estimate average compositions of near-primary, ‘reference’ ocean island basalts (OIBs) for 120 volcanic centers from 31 major island groups and constrain the depth of lithosphere–asthenosphere boundary (LAB) at the time of volcanism and the possible depth of melt–mantle equilibration based on recently calibrated melt silica activity barometer. The LAB depth versus fractionation corrected OIB compositions (lava compositions, X, corrected to Mg# 73, XOIB#73, i.e., magmas in equilibrium with Fo90, if olivine is present in the mantle source) show an increased major element compositional variability with increasing LAB depths. OIBs erupted on lithospheres < 40 km thick approach the compositions (e.g. SiO2#73, TiO2#73, [CaO/Al2O3]#73) of primitive ridge basalts and are influenced strongly by depth and extent of shallow melting. However, XOIB#73 on thicker lithospheres cannot be explained by melt–mantle equilibration as shallow as LAB. Melt generation from a somewhat deeper (up to 50 km deeper than the LAB) peridotite source can explain the OIB major element chemistry on lithospheres ≤ 70 km. However, deeper melting of volatile-free, fertile peridotite is not sufficient to explain the end member primary OIBs on ≥ 70 km thick lithospheres. Comparison between XOIB#73 and experimental partial melts of fertile peridotite indicates that at least two additional melt components need to be derived from OIB source regions. The first component, similar to that identified in HIMU lavas, is characterized by low SiO2#73, Al2O3#73, [Na2O/TiO2]#73, and high FeO?#73, CaO#73, [CaO/Al2O3]#73. The second component, similar to that found in Hawaiian Koolau lavas, is characterized by high SiO2#73, moderately high FeO?#73, and low CaO#73 and Al2O3#73. These two components are not evenly sampled by all the islands, suggesting a heterogeneous distribution of mantle components that generate them. We suggest that carbonated eclogite and volatile-free, silica-excess eclogite are the two most likely candidates, which in conjunction with fertile mantle peridotite, give rise to the two primitive OIB end members.  相似文献   

15.
Serpentinization of the mantle wedge is an important process that influences the seismic and mechanical properties in subduction zones. Seismic detection of serpentines relies on the knowledge of elastic properties of serpentinites, which thus far has not been possible in the absence of single-crystal elastic properties of antigorite. The elastic constants of antigorite, the dominant serpentine at high-pressure in subduction zones, were measured using Brillouin spectroscopy under ambient conditions. In addition, antigorite lattice preferred orientations (LPO) were determined using an electron back-scattering diffraction (EBSD) technique. Isotropic aggregate velocities are significantly lower than those of peridotites to allow seismic detection of serpentinites from tomography. The isotropic VP/VS ratio is 1.76 in the Voigt–Reuss–Hill average, not very different from that of 1.73 in peridotite, but may vary between 1.70 and 1.86 between the Voigt and Reuss bonds. Antigorite and deformed serpentinites have a very high seismic anisotropy and remarkably low velocities along particular directions. VP varies between 8.9 km s? 1 and 5.6 km s? 1 (46% anisotropy), and 8.3 km s? 1 and 5.8 km s? 1 (37%), and VS between 5.1 km s? 1 and 2.5 km s? 1 (66%), and 4.7 km s? 1 and 2.9 km s? 1 (50%) for the single-crystal and aggregate, respectively. The VP/VS ratio and shear wave splitting also vary with orientation between 1.2 and 3.4, and 1.3 and 2.8 for the single-crystal and aggregate, respectively. Thus deformed serpentinites can present seismic velocities similar to peridotites for wave propagation parallel to the foliation or lower than crustal rocks for wave propagation perpendicular to the foliation. These properties can be used to detect serpentinite, quantify the amount of serpentinization, and to discuss relationships between seismic anisotropy and deformation in the mantle wedge. Regions of high VP/VS ratios and extremely low velocities in the mantle wedge of subduction zones (down to about 6 and 3 km.s?1 for VP and VS, respectively) are difficult to explain without strong preferred orientation of serpentine. Local variations of anisotropy may result from kilometer-scale folding of serpentinites. Shear wave splittings up to 1–1.5 s can be explained with moderately thick (10–20 km) serpentinite bodies.  相似文献   

16.
Seismic analysis and geochemical interpretations provide evidence that two separate hydrothermal cells circulate within the greater Lassen hydrothermal system. One cell originates south to SW of Lassen Peak and within the Brokeoff Volcano depression where it forms a reservoir of hot fluid (235–270 °C) that boils to feed steam to the high-temperature fumarolic areas, and has a plume of degassed reservoir liquid that flows southward to emerge at Growler and Morgan Hot Springs. The second cell originates SSE to SE of Lassen Peak and flows southeastward along inferred faults of the Walker Lane belt (WLB) where it forms a reservoir of hot fluid (220–240 °C) that boils beneath Devils Kitchen and Boiling Springs Lake, and has an outflow plume of degassed liquid that boils again beneath Terminal Geyser. Three distinct seismogenic zones (identified as the West, Middle, and East seismic clusters) occur at shallow depths (< 6 km) in Lassen Volcanic National Park, SW to SSE of Lassen Peak and adjacent to areas of high-temperature (≤ 161 °C) fumarolic activity (Sulphur Works, Pilot Pinnacle, Little Hot Springs Valley, and Bumpass Hell) and an area of cold, weak gas emissions (Cold Boiling Lake). The three zones are located within the inferred Rockland caldera in response to interactions between deeply circulating meteoric water and hot brittle rock that overlies residual magma associated with the Lassen Volcanic Center. Earthquake focal mechanisms and stress inversions indicate primarily N–S oriented normal faulting and E–W extension, with some oblique faulting and right lateral shear in the East cluster. The different focal mechanisms as well as spatial and temporal earthquake patterns for the East cluster indicate a greater influence by regional tectonics and inferred faults within the WLB. A fourth, deeper (5–10 km) seismogenic zone (the Devils Kitchen seismic cluster) occurs SE of the East cluster and trends NNW from Sifford Mountain toward the Devils Kitchen thermal area where fumarolic temperatures are ≤ 123 °C. Lassen fumaroles discharge geothermal gases that indicate mixing between a N2-rich, arc-type component and gases derived from air-saturated meteoric recharge water. Most gases have relatively weak isotopic indicators of upper mantle or volcanic components, except for gas from Sulphur Works where δ13C–CO2, δ34S–H2S, and δ15N–N2 values indicate a contribution from the mantle and a subducted sediment source in an arc volcanic setting.  相似文献   

17.
Coupled 187Os/188Os and highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, and Re) abundance data are reported for pristine lunar crustal rocks 60025, 62255, 65315 (ferroan anorthosites, FAN) and 76535, 78235, 77215 and a norite clast in 15455 (magnesian-suite rocks, MGS). Osmium isotopes permit more refined discrimination than previously possible of samples that have been contaminated by meteoritic additions and the new results show that some rocks, previously identified as pristine, contain meteorite-derived HSE. Low HSE abundances in FAN and MGS rocks are consistent with derivation from a strongly HSE-depleted lunar mantle. At the time of formation, the lunar floatation crust, represented by FAN, had 1.4 ± 0.3 pg g? 1 Os, 1.5 ± 0.6 pg g? 1 Ir, 6.8 ± 2.7 pg g? 1 Ru, 16 ± 15 pg g? 1 Pt, 33 ± 30 pg g? 1 Pd and 0.29 ± 0.10 pg g? 1 Re (～ 0.00002 × CI) and Re/Os ratios that were modestly elevated (187Re/188Os = 0.6 to 1.7) relative to CI chondrites. MGS samples are, on average, characterised by more elevated HSE abundances (～ 0.00007 × CI) compared with FAN. This either reflects contrasting mantle-source HSE characteristics of FAN and MGS rocks, or different mantle–crust HSE fractionation behaviour during production of these lithologies. Previous studies of lunar impact-melt rocks have identified possible elevated Ru and Pd in lunar crustal target rocks. The new results provide no supporting evidence for such enrichments.If maximum estimates for HSE in the lunar mantle are compared with FAN and MGS averages, crust–mantle concentration ratios (D-values) must be ≤ 0.3. Such D-values are broadly similar to those estimated for partitioning between the terrestrial crust and upper mantle, with the notable exception of Re. Given the presumably completely different mode of origin for the primary lunar floatation crust and tertiary terrestrial continental crust, the potential similarities in crust–mantle HSE partitioning for the Earth and Moon are somewhat surprising. Low HSE abundances in the lunar crust, coupled with estimates of HSE concentrations in the lunar mantle implies there may be a ‘missing component’ of late-accreted materials (as much as 95%) to the Moon if the Earth/Moon mass-flux estimates are correct and terrestrial mantle HSE abundances were established by late accretion.  相似文献   

18.
Li isotopic compositions of magmatic rocks have gained considerable attention recently as probes of mantle-scale processes. However, the concentrations and isotopic composition of Li in mantle minerals from mid-ocean ridges remain relatively unconstrained. This is largely because of the general presence of seawater alteration in abyssal peridotites. Lithium elemental and isotopic compositions for mineral separates of coexisting olivine, clinopyroxene, orthopyroxene and bulk rocks of serpentine-free Gakkel Ridge peridotites were investigated. Bulk rocks have Li contents of 1.6 to 2.7 ppm and δ7Li values of 3 to 5‰, which fall within the range of reported normal pristine “MORB mantle” values. Lithium concentrations vary in the order cpx (2.1–4.7 ppm) > opx (0.9–1.7 ppm) ≥ olivine (0.4–0.9 ppm), the opposite found in “equilibrated” mantle peridotite xenoliths (Seitz and Woodland, 2000). The Li isotopic compositions indicate a systematic mineral variation with δ7Liolivine (7.14‰–15.09‰) > δ7Liopx (1.81‰–3.66‰) > δ7Licpx (?2.43‰ ? ?0.39‰). The δ7Li values of cpx are negatively correlated with their Li concentrations with the lightest value for the most enriched cpx grains. There is a first order negative linear correlation between Δolivine–cpx (δ7Liolivine ? δ7Licpx) and ol/cpxD (Liolivine/Licpx).Numerical simulations indicate that the observed systematic inter-mineral variations of Li concentrations and isotopic compositions could be explained by a cooling driven diffusive redistribution between minerals in a closed system if there is a temperature dependent partitioning of Li between olivine and clinopyroxene. The studied Gakkel Ridge abyssal peridotites may alternatively have cooled under a variable cooling rate with a rapid cooling before the Li system was closed, which is less likely given the tectonic setting. Our calculations confirm that Li systematics in minerals, especially in coexisting mineral phases could potentially be used as a mantle geospeedometer, even for slowly cooled mantle rocks.  相似文献   

19.
Adsorption of Pb2+ from aqueous solution onto a sugarcane bagasse/multi-walled carbon nanotube (MWCNT) composite was investigated by using a series of batch adsorption experiments and compared with the metal uptake ability of sugarcane bagasse. The efficiency of the adsorption processes was studied experimentally at various pH values, contact times, adsorbent masses, temperatures and initial Pb2+ concentrations. A pH of 4.5 was found to be the optimum pH to obtain a maximum adsorption percentage in 120 min of equilibration time. The composite showed a much enhanced adsorption capacity for Pb2+ of 56.6 mg g−1 compared with 23.8 mg g−1 for bagasse at 28 °C. The Langmuir adsorption isotherm provided the best fit to the equilibrium adsorption data. The pseudo first-order, pseudo second-order, intraparticle diffusion and Elovich kinetics models were used to analyse the rate of lead adsorption and the results show that the Elovich model is more suitable. The thermodynamic parameters of adsorption, namely ΔG°, ΔH° and ΔS°, were determined over the temperature range of 20–45 °C. The adsorption of Pb2+ onto both bagasse and the sugarcane bagasse/MWCNT composite was found to be spontaneous but for the former adsorbent it was enthalpy-driven whereas for the latter it was entropy-driven. Desorption of the lead-loaded adsorbents was fairly efficient with 0.1 mol dm−3 HCl. Overall this composite has the potential to be a good adsorbent for the removal of Pb2+ from wastewaters.  相似文献   

20.
Boa Vista, the easternmost island in the Cape Verde archipelago, consists of volcanic products, minor intrusions and a thin partial sedimentary cover. The first 15 age results from 40Ar/39Ar incremental heating analysis of groundmass separates from volcanic and plutonic rocks from Boa Vista are presented. The combination of age results and field observations demonstrates that the volcanic activity that formed the island occurred in three main stages: (1) > 16 Ma, (2) 15–12.5 Ma and (3) 9.5–4.5 Ma. The first stage, restricted to the north eastern part of the island, is dominated by ankaramitic lavas. The second stage, consisting of evolved lavas of phonolitic–trachytic compositions and nepheline syenites, makes up large central parts of the island. The large volume of evolved rocks and the extended eruption period of several Ma make stage 2 in Boa Vista unique to Cape Verde. Mainly basanites and nephelinites were erupted during the third stage, initially dominated by eruption of subaerial mafic lavas around 9 Ma. Pillow lavas are erupted around 7 Ma whereupon dominantly subaerial mafic lavas were erupted. Stage 3 saw volcanism in many centres distributed mainly along the present coastline and with activity partly overlapping in time. The volcanic evolution of Boa Vista constrains the initiation of volcanic activity in the Cape Verde archipelago to the eastern islands. Major and trace element geochemistry of 160 volcanic and plutonic rocks representing the entire exposed chronological sequence on Boa Vista is presented, revealing an extremely well developed Daly Gap. Only a little was modified from the mafic magmas that rose in small batches from the mantle. Compositional variation distinguishes each volcanic complex and was to a large extent present in the mantle melts. The highly evolved stage 2 phonolites and trachytes are related through the fractional crystallization of three compositionally distinct magmas. Two of these may have been derived by crystal fractionation of primitive Boa Vista melts, whereas the third was not.  相似文献   

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