Hf–Nd isotopic decoupling in continental mantle lithosphere beneath Northeast China: Effects of pervasive mantle metasomatism

Nd–Hf isotopic decoupling has frequently been observed in the continental and oceanic mantle, but its origin remains controversial. Here we present combined elemental and Sr–Nd–Hf isotopic study on peridotite xenoliths entrained in Cenozoic basalts from Shuangliao and Jiaohe in Northeast China, which provides insight into this issue. The data reveal a heterogeneous lithospheric mantle beneath Northeastern China, consisting of fertile (type I) to strongly refractory (type II) peridotites. Type I peridotites are largely shielded from late metasomatism, thus preserving information of depletion events. Nd model age suggests a Proterozoic lithospheric mantle beneath NE China. Type II peridotites are mostly refractory harzburgites and show ubiquitous enrichment of incompatible elements. They are further divided into two sub-groups. Clinopyroxenes from type IIa samples have high and wide Lu/Hf (0.34–1.3) and very radiogenic Hf isotopic ratios (ε_Hf = 44.4–63.8). Hf concentration is generally low (0.12–0.43 ppm) and plots along or slightly above the modeled partial melting depletion trend. In contrast, Nd content in type IIa clinopyroxenes is significantly higher than the modeled concentrations in residues at a given degree of melt depletion. The difference in enrichment of Hf and Nd translates to decoupling of Lu/Hf–Sm/Nd ratios and of Nd–Hf isotopes (ε_Nd = −1.3 to 8.4). Clinopyroxenes from most of type IIb peridotites have relatively low Lu/Hf ratios (0.04–0.24) and coupled Nd–Hf isotopes. Both Hf and Nd plot significantly above the depletion trend; their concentrations are governed by the equilibrium partitioning between percolating melt and peridotites. The distinct geochemical characteristics of type IIa and type IIb clinopyroxenes may have resulted from chromatographic percolation of small volumes of silicate melts, in which percolation fronts of incompatible elements are dependent on their relative incompatibilities.     

Trace element and isotope geochemistry of depleted peridotites from an N-MORB type ophiolite (Internal Liguride,N. Italy)

 Mantle peridotites of the Internal Liguride (IL) units (Northern Apennines) constitute a rare example of the depleted lithosphere of the Jurassic Ligurian Tethys. Detailed chemical (ICP-MS and SIMS techniques) and isotopic investigations on very fresh samples have been performed with the major aim to constrain the timing and mechanism of their evolution and to furnish new data for the geodynamic interpretation. The data are also useful to discuss some general geochemical aspects of oceanic-type mantle. The studied samples consist of clinopyroxene-poor spinel lherzolites, showing incipient re-equilibration in the plagioclase-facies stability field. The spinel-facies assemblage records high (asthenospheric) equilibration temperatures (1150–1250° C). Whole rocks, and constituent clinopyroxenes, show a decoupling between severe depletion in highly incompatible elements [light rare earth elements (LREE), Sr, Zr, Na, Ti] and less pronounced depletion in moderate incompatible elements (Ca, Al, Sc, V). Bulk rocks also display a relatively strong M(middle)REE/H(heavy)REE fractionation. These compositional features indicate low-degree (<10%) fractional melting, which presumably started in the garnet stability field, as the most suitable depletion mechanism. In this respect, the IL ultramafics show strong similarity to abyssal peridotites. The Sr and Nd isotopic compositions, determined on carefully handpicked clinopyroxene separates, indicate an extremely depleted signature (⁸⁷Sr/⁸⁶Sr=0.702203–0.702285; ¹⁴³Nd/¹⁴⁴Nd=0.513619–0.513775). The Sm/Nd model ages suggest that the IL peridotites melted most likely during Permian times. They could record, therefore, the early upwelling and melting of mid ocean ridge basalt (MORB) type asthenosphere, in response to the onset of extensional mechanisms which led to the opening of the Western Tethys. They subsequently cooled and experienced a composite subsolidus evolution testified by multiple episodes of gabbroic intrusions and HT-LP retrograde metamorphic re-equilibration, prior to their emplacement on the sea floor. The trace element chemistry of IL peridotites also provides useful information about the composition of oceanic-type mantle. The most important feature concerns the occurrence of Sr and Zr negative anomalies (relative to “adjacent” REE) in both clinopyroxenes and bulk rocks. We suggest that such anomalies reflect changes in the relative magnitude of Sr, Zr and REE partition coefficients, depending on the specific melting conditions. Received: 15 February 1995/Accepted: 4 August 1995     

Permian basaltic rocks in the Tarim basin, NW China: Implications for plume–lithosphere interaction

There are large areas of Permian basaltic rocks in the Tarim basin (PBRT) in northwestern China. Precise Ar–Ar dating of these rocks revealed an eruption age span of 262 to 285 Ma. Most of the PBRT is composed of alkaline basaltic rocks with high TiO₂ (2.43%–4.59%, weight percent), high Fe₂O₃ + FeO (12.63%–17.83%) and P₂O₅ (0.32%–1.38%) contents. Trace elements of these rocks have affinities with oceanic island basalts (OIB), as shown in chondrite normalized rare earth elements (REE) diagrams and primitive mantle normalized incompatible elements diagrams. The rocks show complex Sr–Nd isotopic character based on which they can be subdivided into two distinct groups: group 1 has relatively small initial (t = 280 Ma)⁸⁷Sr/⁸⁶Sr ratio ( 0.7048) and positive εNd(t) (3.42–4.66) values. Group 2 has relatively large initial ⁸⁷Sr/⁸⁶Sr ratio (0.7060–0.7083) and negative εNd(t) (from − 2.79 to − 2.16) values. Lead isotopes are even more complex with variations of (²⁰⁶Pb/²⁰⁴Pb)t, (²⁰⁷Pb/²⁰⁴Pb)t and (²⁰⁸Pb/²⁰⁴Pb)t ranging from 17.9265 to 18.5778, 15.4789 to 15.6067 and 37.2922 to 38.1437, respectively. Moreover, these two groups have different trace elements ratios such as Nb/La, Ba/Nb, Zr/Nb, Nb/Ta and Zr/Hf, implying different magmatic processes. Based on the geochemistry of basaltic rocks and an evaluation of the tectonics, deformation, and the compositions of crust and lithospheric mantle in Tarim, we conclude that these basaltic rocks resulted from plume–lithosphere interaction. Permian mantle plume caused an upwelling of the Tarim lithosphere leading to melting of the asthenospheric mantle by decompression. The magma ascended rapidly to the base of lower crust, where different degrees of assimilation of OIB-like materials and fractionation occurred. Group 1 rocks formed where the upwelling is most pronounced and the assimilation was negligible. In other places, different degrees of assimilation and fractionation account for the geochemical traits of group 2.     

Geochemistry of peridotites from the Yap Trench,Western Pacific: implications for subduction zone mantle evolution

ABSTRACT

This study examines the major and trace elements of peridotites from the Yap Trench in the western Pacific to investigate mantle evolution beneath a subduction zone. Major element results show that the peridotites are low in Al₂O₃ (0.31–0.65 wt.%) and CaO (0.04–0.07 wt.%) contents and high in Mg# (Mg/(Mg+Fe)) (0.91–0.92) and have spinels with Cr# (Cr/(Cr+Al)) higher than 0.6 (0.61–0.73). Trace element results show that the peridotites have extremely low heavy rare earth element (HREE) contents compared with abyssal peridotites but have U-shaped chondrite-normalized rare earth element (REE) patterns. The degree of mantle melting estimated based on the major elements, HREEs, and spinel Cr# range from 19% to 25%, indicating that the Yap Trench peridotites may be residues of melting associated with the presence of water in the mantle source. In addition to light rare earth element (LREE) enrichment, the peridotites are characterized by high contents of highly incompatible elements, positive U and Sr anomalies, negative Ti anomalies, and high Zr/Hf ratios. The correlations between these elements and both the degree of serpentinization and high field strength element (HFSE) contents suggest that fluid alteration alone cannot account for the enrichment of the peridotites and that at least the enrichment of LREEs was likely caused by melt–mantle interaction. Comparison between the peridotites and the depletion trend defined by the primitive mantle (PM) and the depleted mantle (DM) suggests that the Yap Trench mantle was modified by subduction-related melt characterized by high contents of incompatible elements, high Zr/Hf ratios, and low HFSE contents. Hydrous melting may have been enhanced by tectonic erosion of the subducting Caroline Plate with complex tectonic morphostructures at the earliest stages of subduction initiation.     

Chemical and chronologic complexity in the convecting upper mantle: Evidence from the Taitao ophiolite, southern Chile

Exposure of the ca. 6 Ma Taitao ophiolite, Chile, located 50 km south of the Chile Triple Junction, allows detailed chemical and isotopic study of rocks that were recently extracted from the depleted mantle source of mid-ocean ridge basalts (DMM). Ultramafic and mafic rocks are examined for isotopic (Os, Sr, Nd, and O), and major and trace element compositions, including the highly siderophile elements (HSE). Taitao peridotites have compositions indicative of variable extents of partial melting and melt extraction. Low δ¹⁸O values for most whole rock samples suggest some open-system, high-temperature water–rock interaction, most likely during serpentinization, but relict olivine grains have δ¹⁸O values consistent with primary mantle values. Most of the peridotites analyzed for Nd–Sr isotopes have compositions consistent with estimates for the modern DMM, although several samples are characterized by ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd indicative of crustal contamination, most likely via interactions with seawater. The peridotites have initial ¹⁸⁷Os/¹⁸⁸Os ratios that range widely from 0.1168 to 0.1288 (γ_Os = −8.0 to +1.1), averaging 0.1239 (γ_Os = −2.4), which is comparable to the average for modern abyssal peridotites. A negative correlation between the Mg^# of relict olivine grains and Os isotopic compositions of whole rock peridotites suggests that the Os isotopic compositions reflect primary mantle Re/Os fractionation produced by variable extents of partial melting at approximately 1.6 Ga. Recent re-melting at or near the spatially associated Chile Ridge further modified these rocks, and Re, and minor Pt and Pd were subsequently added back into some rocks by late-stage melt–rock or fluid–rock interactions.In contrast to the peridotites, approximately half of the mafic rocks examined have whole rock δ¹⁸O values within the range of mantle compositions, and their Nd and Sr isotopic compositions are all generally within the range of modern DMM. These rocks have initial ¹⁸⁷Os/¹⁸⁸Os ratios, calculated for 6 Ma, that range from 0.126 (γ_Os = −1) to as high as 0.561 (γ_Os = +342). The Os isotopic systematics of each of these rocks may reflect derivation from mixed lithologies that include the peridotites, but may also include pyroxenites with considerably more radiogenic Os than the peridotites. This observation supports the view that suprachondritic Os present in MORB derives from mixed mantle source lithologies, accounting for some of the worldwide dichotomy in ¹⁸⁷Os/¹⁸⁸Os between MORB and abyssal peridotites.The collective results of this study suggest that this >500 km³ block of the mantle underwent at least two stages of melting. The first stage occurred at 1.6 Ga, after which the block remained isolated and unmixed within the DMM. A final stage of melting recently occurred at or near the Chile Ridge, resulting in the production of at least some of the mafic rocks. Convective stirring of this mantle domain during a >1 Ga period was remarkably inefficient, at least with regard to Os isotopes.     

Chronology, Petrology and Isotope Geochemistry of the Erro-Tobbio Peridotites (Ligurian Alps, Italy): Records of Late Palaeozoic Lithospheric Extension

Mantle peridotites from the Erro–Tobbio (ET) ophioliticunit (Voltri Massif, Ligurian Alps) record a tectono-metamorphicdecompressional evolution, indicated by re-equilibration fromspinel- to plagioclase- to amphibole-facies conditions, andprogressive deformation from granular to tectonite to mylonitefabrics. The peridotites are considered to represent subcontinentallithospheric mantle that was tectonically denuded during riftingand opening of the Jurassic Ligurian Tethys ocean, similar tothe Northern Apennine (External Ligurides) ophiolitic peridotites.We performed chemical and isotopic investigations on selectedgranular and tectonite spinel peridotites and plagioclase tectonitesand mylonites, with the aim of defining the nature of the mantleprotoliths, and to date the onset of exhumation of the ET peridotites.Spinel- and plagioclase-bearing tectonites and mylonites exhibitheterogeneous bulk-rock major and trace element composition,despite rather homogeneous mineral chemistry, thus indicatingthat the ET mantle protoliths record a composite history ofpartial melting and melt migration by reactive porous flow.The lack of correlation between the observed geochemical heterogeneityand the structural type (granular, tectonite, mylonite) indicatesthat the inferred reactive porous flow event preceded the exhumation-relatedlithospheric history of the Erro–Tobbio mantle. The tectono-metamorphicevolution caused systematic chemical changes in minerals: (1)Al decrease in orthopyroxene; (2) Al decrease, and Cr and Tiincrease in spinels; (3) Al and Sr decrease, Cr, Ti, Zr, Sc,V and middle to heavy rare earth element increase and developmentof a negative Eu anomaly in clinopyroxene. The studied sampleshave Nd isotope compositions consistent with a mid-ocean ridgebasalt mantle reservoir. Sm/Nd isotope data on plagioclase andclinopyroxene separates (and corresponding whole rocks) fromtwo plagioclase peridotites, representative of the plagioclase-bearingmylonitic extensional shear zone, have yielded ages of 273 ±16 Ma and 313 ± 16 Ma, for the plagioclase-facies recrystallizationstage, significantly older than the expected Jurassic age. Thisindicates that the Erro–Tobbio peridotites represent subcontinentallithospheric mantle that was tectonically exhumed from spinel-faciesdepths to shallower lithospheric levels during Late Carboniferous–Permiantimes. Our results are consistent with the previously documentedevidence for an extensional regime in the Europe–Adrialithosphere during Late Palaeozoic time, and they representthe first record that extensional mechanisms were also activeat lithospheric mantle levels. KEY WORDS: plagioclase-bearing peridotites; subcontinental lithospheric mantle; mantle exhumation; Sm/Nd dating     

Petrology of Karoo volcanic rocks in the southern Lebombo monocline, Mozambique

The Karoo volcanic sequence in the southern Lebombo monocline in Mozambique contains different silicic units in the form of pyroclastic rocks, and two different basalt types. The silicic units in the lower part of the Lebombo sequence are formed by a lower unit of dacites and rhyolites (67–80 wt.% SiO₂) with high Ba (990–2500 ppm), Zr (800–1100 ppm) and Y (130–240 ppm), which are part of the Jozini–Mbuluzi Formation, followed by a second unit, interlayered with the Movene basalts, of high-SiO₂ rhyolites (76–78 wt.%; the Sica Beds Formation), with low Sr (19–54 ppm), Zr (340–480 ppm) and Ba (330–850 ppm) plus rare quartz-trachytes (64–66 wt.% SiO₂), with high Nb and Rb contents (240–250 and 370–381 ppm, respectively), and relatively low Zr (450–460 ppm). The mafic rocks found at the top of the sequence are basalts and ferrobasalts belonging to the Movene Formation. The basalts have roughly flat mantle-normalized incompatible element patterns, with abundances of the most incompatible elements not higher than 25 times primitive mantle. The ferrobasalt has TiO₂  4.7 wt.%, Fe₂O_3t = 16 wt.%, and high Y (100 ppm), Zr (420 ppm) and Ba (1000 ppm). The Movene basalts have initial (at 180 Ma) ⁸⁷Sr/⁸⁶Sr = 0.7052–0.7054 and ¹⁴³Nd/¹⁴⁴Nd = 0.51232, and the Movene ferrobasalt has even lower ⁸⁷Sr/⁸⁶Sr (0.70377) and higher ¹⁴³Nd/¹⁴⁴Nd (0.51259). The silicic rocks show a modest range of initial Sr-(⁸⁷Sr/⁸⁶Sr = 0.70470–0.70648) and Nd-(¹⁴³Nd/¹⁴⁴Nd = 0.51223–0.51243) isotope ratios. The less evolved dacites could have been formed after crystal fractionation of oxide-rich gabbroic cumulates from mafic parental magmas, whereas the most silica-rich rhyolites could have been formed after fractional crystallization of feldspars, pyroxenes, oxides, zircon and apatite from a parental dacite magma. The composition of the Movene basalts imply different feeding systems from those of the underlying Sabie River basalts.     

Ultramafic Xenoliths from the Bearpaw Mountains, Montana, USA: Evidence for Multiple Metasomatic Events in the Lithospheric Mantle beneath the Wyoming Craton

Ultramafic xenoliths in Eocene minettes of the Bearpaw Mountainsvolcanic field (Montana, USA), derived from the lower lithosphereof the Wyoming craton, can be divided based on textural criteriainto tectonite and cumulate groups. The tectonites consist ofstrongly depleted spinel lherzolites, harzburgites and dunites.Although their mineralogical compositions are generally similarto those of spinel peridotites in off-craton settings, somecontain pyroxenes and spinels that have unusually low Al₂O₃contents more akin to those found in cratonic spinel peridotites.Furthermore, the tectonite peridotites have whole-rock majorelement compositions that tend to be significantly more depletedthan non-cratonic mantle spinel peridotites (high MgO, low CaO,Al₂O₃ and TiO₂) and resemble those of cratonic mantle. Thesecompositions could have been generated by up to 30% partialmelting of an undepleted mantle source. Petrographic evidencesuggests that the mantle beneath the Wyoming craton was re-enrichedin three ways: (1) by silicate melts that formed mica websteriteand clinopyroxenite veins; (2) by growth of phlogopite fromK-rich hydrous fluids; (3) by interaction with aqueous fluidsto form orthopyroxene porphyroblasts and orthopyroxenite veins.In contrast to their depleted major element compositions, thetectonite peridotites are mostly light rare earth element (LREE)-enrichedand show enrichment in fluid-mobile elements such as Cs, Rb,U and Pb on mantle-normalized diagrams. Lack of enrichment inhigh field strength elements (HFSE; e.g. Nb, Ta, Zr and Hf)suggests that the tectonite peridotites have been metasomatizedby a subduction-related fluid. Clinopyroxenes from the tectoniteperidotites have distinct U-shaped REE patterns with strongLREE enrichment. They have ¹⁴³Nd/¹⁴⁴Nd values that range from0·5121 (close to the host minette values) to 0·5107,similar to those of xenoliths from the nearby Highwood Mountains.Foliated mica websterites also have low ¹⁴³Nd/¹⁴⁴Nd values (0·5113)and extremely high ⁸⁷Sr/⁸⁶Sr ratios in their constituent phlogopite,indicating an ancient (probably mid-Proterozoic) enrichment.This enriched mantle lithosphere later contributed to the formationof the high-K Eocene host magmas. The cumulate group rangesfrom clinopyroxene-rich mica peridotites (including abundantmica wehrlites) to mica clinopyroxenites. Most contain >30%phlogopite. Their mineral compositions are similar to thoseof phenocrysts in the host minettes. Their whole-rock compositionsare generally poorer in MgO but richer in incompatible traceelements than those of the tectonite peridotites. Whole-rocktrace element patterns are enriched in large ion lithophileelements (LILE; Rb, Cs, U and Pb) and depleted in HFSE (Nb,Ta Zr and Hf) as in the host minettes, and their Sr–Ndisotopic compositions are also identical to those of the minettes.Their clinopyroxenes are LREE-enriched and formed in equilibriumwith a LREE-enriched melt closely resembling the minettes. Thecumulates therefore represent a much younger magmatic event,related to crystallization at mantle depths of minette magmasin Eocene times, that caused further metasomatic enrichmentof the lithosphere. KEY WORDS: ultramafic xenoliths; Montana; Wyoming craton; metasomatism; cumulates; minette     

Spinel peridotite xenoliths from the Atsagin-Dush volcano, Dariganga lava plateau, Mongolia: a record of partial melting and cryptic metasomatism in the upper mantle

Spinel peridotite xenoliths from the Atsagin-Dush volcanic centre, SE Mongolia range from fertile lherzolites to clinopyroxene(cpx)-bearing harzburgites. The cpx-poor peridotites typically contain interstitial fine-grained material and silicate glass and abundant fluid inclusions in minerals, some have large vesicular melt pockets that apparently formed after primary clinopyroxene and spinel. No volatile-bearing minerals (amphibole, phlogopite, apatite, carbonate) have been found in any of the xenoliths. Fifteen peridotite xenoliths have been analysed for major and trace elements; whole-rock Sr isotope compositions and O isotope composition of all minerals were determined for 13 xenoliths. Trace element composition and Sr-Nd isotope compositions were also determined in 11 clinopyroxene and melt pocket separates. Regular variations of major and moderately incompatible trace elements (e.g. heavy-rare-earth elements) in the peridotite series are consistent with its formation as a result of variable degrees of melt extraction from a fertile lherzolite protolith. The Nd isotope compositions of LREE (light-rare-earth elements)-depleted clinopyroxenes indicate an old (≥ 1 billion years) depletion event. Clinopyroxene-rich lherzolites are commonly depleted in LREE and other incompatible trace elements whereas cpx-poor peridotites show metasomatic enrichment that can be related to the abundance of fine-grained interstitial material, glass and fluid inclusions in minerals. The absence of hydrous minerals, ubiquitous CO₂-rich microinclusions in the enriched samples and negative anomalies of Nb, Hf, Zr, and Ti in primitive mantle-normalized trace element patterns of whole rocks and clinopyroxenes indicate that carbonate melts may have been responsible for the metasomatic enrichment. Low Cu and S contents and high δ³⁴S values in whole-rock peridotites could be explained by interaction with oxidized fluids that may have been derived from subducted oceanic crust. The Sr-Nd isotope compositions of LREE-depleted clinopyroxenes plot either in the MORB (mid-ocean-ridge basalt) field or to the right of the mantle array, the latter may be due to enrichment in radiogenic Sr. The LREE-enriched clinopyroxenes and melt pockets plot in the ocean island-basalt field and have Sr-Nd isotope signatures consistent with derivation from a mixture of the DMM (depleted MORB mantle) and EM (enriched mantle) II sources. Received: 18 January 1996 / Accepted: 23 August 1996     

<Superscript>10</Superscript>Be, <Superscript>18</Superscript>O and radiogenic isotopic constraints on the origin of adakitic signatures: a case study from Solander and Little Solander Islands,New Zealand

Subduction-related Quaternary volcanic rocks from Solander and Little Solander Islands, south of mainland New Zealand, are porphyritic trachyandesites and andesites (58.20–62.19 wt% SiO₂) with phenocrysts of amphibole, plagioclase and biotite. The Solander and Little Solander rocks are incompatible element enriched (e.g. Sr ~931–2,270 ppm, Ba ~619–798 ppm, Th ~8.7–21.4 ppm and La ~24.3–97.2 ppm) with MORB-like Sr and Nd isotopic signatures. Isotopically similar quench-textured enclaves reflect mixing with intermediate (basaltic-andesite) magmas. The Solander rocks have geochemical affinities with adakites (e.g. high Sr/Y and low Y), whose origin is often attributed to partial melting of subducted oceanic crust. Solander sits on isotopically distinct continental crust, thus excluding partial melting of the lower crust in the genesis of the magmas. Furthermore, the incompatible element enrichments of the Solander rocks are inconsistent with partial melting of newly underplated mafic lower crust; reproduction of their major element compositions would require unrealistically high degrees of partial melting. A similar argument precludes partial melting of the subducting oceanic crust and the inability to match the observed trace element patterns in the presence of residual garnet or plagioclase. Alternatively, an enriched end member of depleted MORB mantle source is inferred from Sr, Nd and Pb isotopic compositions, trace element enrichments and εHf ? 0 CHUR in detrital zircons, sourced from the volcanics. ¹⁰Be and Sr, Nd and Pb isotopic systematics are inconsistent with significant sediment involvement in the source region. The trace element enrichments and MORB-like Sr and Nd isotopic characteristics of the Solander rocks require a strong fractionation mechanism to impart the high incompatible element concentrations and subduction-related (e.g. high LILE/HFSE) geochemical signatures of the Solander magmas. Trace element modelling shows that this can be achieved by very low degrees of melting of a peridotitic source enriched by the addition of a slab-derived melt. Subsequent open-system fractionation, involving a key role for mafic magma recharge, resulted in the evolved andesitic adakites.     

Case studies on the origin of basalt: III. Petrogenesis of the Mauna Ulu eruption,Kilauea, 1969–1971

During the Mauna Ulu flank eruption on Kilauea, Hawaii, the concentrations in the lavas of the minor elements K, P, Na and Ti, and the incompatible trace elements (analyzed by isotope dilution) K, Rb, Cs, Ba, Sr, and the REE (except Yb) decreased monotonically and linearly with the time (or date) of the eruption. At the same time, the concentrations of the major elements and of Yb, and the ratios of K/Rb, K/Cs, Ba/Rb, ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd remained constant. Most of the scatter in the raw concentration data is removed by a simple correction for olivine (plus chromite) fractionation previously established by Wright et al. (1975). These results are explained by simple equilibrium partial melting of a uniform source. The degree of melting increased by about 20% of the initial value during the course of the eruption. The trace element data are inverted by the method originated by Minster and Allègre (1978) and simplified by Hofmann and Feigenson (1983). The source has the following element (or isotope) ratios: K/Rb=501±7, Ba/Rb=14.0±0.5, Rb/Cs=95±7, Rb/Sr=0.0193 (+0.0045, –0.0090), (Ce/Ba)_CN= 1.1±0.1, (Sr/Ba)_CN=1.19 (+0.30, –0.19), ⁸⁷Sr/⁸⁶Sr=0.703521±0.000016, and ¹⁴³Nd/¹⁴⁴Nd=0.512966±0.000008. The REE pattern of the source has a nearly flat or slightly negative slope (=relative LREE enrichment) between Ce and Dy and a strongly positive slope between Dy and Yb. However, this relative HREE enrichment is poorly constrained by the analytical data, is highly model dependent and may not be a true source feature. The Yb concentration in the source is particularly poorly constrained because it is essentially constant in the melts. On the other hand, this special feature demonstrates that Yb must be buffered by a mineral phase with a high partition coefficient for Yb, namely garnet. The calculated clinopyroxene/garnet ratio in the source is roughly equal to one. In contrast, the source of Kohala volcano had previously been found to contain little or no garnet.     

Petrogenesis of extension-related alkaline volcanism in Karaburhan (Sivrihisar–Eskisehir), NW Anatolia, Turkey

Alkaline lavas were erupted as phonolites and trachytes around Karaburhan (Sivrihisar–Eskisehir, NW Anatolia) within the Izmir–Ankara–Erzincan suture zone. These volcanic rocks were emplaced as domes, close and parallel to the ophiolite thrust line. According to ⁴⁰Ar/³⁹Ar geochronological analyses of sanidine crystals from the phonolites, the age of the alkaline volcanics is 25 Ma (Late Oligocene–Early Miocene).The flow-textured phonolites are porphyritic and consist mainly of sanidine, clinopyroxene, and feldspathoid crystals. The clinopyroxenes show compositional zoning, with aegirine (Na_0.82–0.96Fe⁺³_0.68–0.83) rims and aegirine–augite cores (containing calcium, magnesium, and Fe⁺²). Some aegirine–augites are replaced with sodium-, calcium-, and magnesium-rich amphibole (hastingsite). Feldspathoid (hauyne) crystals enriched with elemental Na and Ca have been almost completely altered to zeolite and carbonate minerals. The fine-grained trachytes with a trachytic texture consist of feldspar (oligoclase and sanidine) phenocrystals and clinopyroxene microphenocrystals within a groundmass made up largely of alkali feldspar microlites.Although there are some differences in their element patterns, the phonolites and trachytes exhibit enrichment in LILEs (Sr, K, Rb, Ba, Th) and LREEs (La, Ce, Pr, Nd) and negative anomalies in Nb and Ta. These geochemical characteristics indicate a lithospheric mantle enriched by fluids extracted from the subduction component. In addition, the high ⁸⁷Sr/⁸⁶Sr (0.706358–0.708052) and low ¹⁴³Nd/¹⁴⁴Nd (0.512546–0.512646) isotope concentrations of the alkaline lavas reflect a mantle source that has undergone metasomatism by subduction-derived fluids. Petrogenetic modeling indicates that the alkaline lavas generated from the subduction-modified lithospheric mantle have undergone assimilation, fractional crystallization, and crustal contamination, acquiring high Pb, Ba, Rb, and Sr contents and Pb isotopic compositions during their ascent through the thickened crust in an extensional setting.     

Charnockite genesis across the Archaean–Proterozoic terrane boundary in the South Indian Granulite Terrain: Constraints from major–trace element geochemistry and Sr–Nd isotopic systematics

Major, trace element compositions and Sr–Nd isotopic characteristics of charnockitic gneisses from the Southern Granulite Terrain (SGT), South India are presented. The study region encompasses the central segment of the Cauvery Shear Zone system (CSZ) and regions within the Madurai Block (MB) immediately south of it (designated here as the CSZ/MB and MB domains). Differences in the compositions and source characteristics between charnockitic rocks of the CSZ vis-à-vis those of the CSZ/MB and MB regions are highlighted. Foremost, the charnockites and enderbites of the CSZ show highly fractionated REE patterns with positive Eu-anomalies, depleted HREE, Y and near chondritic εNd₀ and initial-⁸⁷Sr/⁸⁶Sr at ca. 2.5 Ga, consistent with hydrous partial melting of amphibolitic crust with residual garnet and hornblende for the parental melts. By contrast, modeled at ca. 1.8 Ga and 0.8 Ga, the CSZ/MB and MB charnockitic rocks, which show a wider range of Ti and P, relatively lower degree of HREE depletion, commonly negative Eu-anomalies and undepleted Y, present clear evidence for involvement of Archaean crustal components in sources of their magmatic protoliths. There is also evidence for significant intracrustal melting processes within a thickened crust at elevated temperatures between 800 and 1000 °C. Implications to the controversial Archaean–Neoproterozoic terrane boundary problem of the SGT are discussed.     

A geochemical study of magmatism associated with the initial stages of back-arc spreading

Bransfield Strait is a narrow basin separating the South Shetland Islands from the Antarctic Peninsula and is attributed to recent back-arc extension behind the South Shetland volcanic arc. The volcanic islands of Deception and Bridgeman are situated close to the axis of spreading, whereas Penguin Island lies slightly to the north of this axis. The mineralogy, petrology and geochemistry of the lavas of the three volcanoes have been studied in order to provide information on the nature of magmatism associated with the initial stages of back-arc spreading.Deception Island lavas range from olivine basalt to dacite, and all are highly sodic, with high Na/K, K/Rb, Ba/Rb and Zr/Nb ratios and with Ce_N/Yb_N = 2. Incompatible elements increase systematically between basalt and rhyodacite, while Sr decreases, suggesting that fractional crystallisation is the dominant process relating lava compositions. The rhyodacites have high concentrations of Zr, Y and the REE and negative Eu anomalies and are compositionally similar to oceanic plagiogranite. Bridgeman Island lavas are mostly basaltic andesites, but the levels of many incompatible elements, including REE, are significantly lower than those of Deception lavas, although Ce_N/Yb_N ratios and ⁸⁷Sr/⁸⁶Sr ratios (0.7035) are the same. Penguin Island lavas are magnesian, mildly alkaline olivine basalts with a small range of composition that can be accommodated by fractional crystallisation of olivine, clinopyroxene and/or chromite. Penguin lavas have higher ⁸⁷Sr/⁸⁶Sr (0.7039) and Ce_N/ Yb_N (4) ratios than Deception and Bridgeman lavas. The Rb/Sr ratios of Deception and Penguin basalts (ca. 0.01) are much too low to account for their present ⁸⁷Sr/⁸⁶Sr ratios.Modelling suggests that the source regions of the lavas of the three volcanoes share many geochemical features, but there are also some significant differences, which probably reflects the complex nature of the mantle under an active island arc combined with complex melting relationships attending the initial stages of back-arc spreading. Favoured models suggest that Bridgeman lavas represent 10–20% melting and the more primitive Deception lavas 5–10% melting of spinel-peridotite, whereas Penguin lavas represent less then 5% melting of a garnet-peridotite source. The mantle source for Bridgeman lavas seems to have undergone short-term enrichment in K, Rb and Ba, possibly resulting from dewatering of the subducted slab. Hydrous melting conditions may also account for the more siliceous, high-alumina nature and low trace element contents of Bridgeman lavas.     

Evolution of the upper mantle beneath the southern Baikal rift zone: an Sr-Nd isotope study of xenoliths from the Bartoy volcanoes

Anhydrous and amphibole-bearing peridotite xenoliths occur in roughly equal quantitites in the Bartoy volcanic field about 100 km south of the southern tip of Lake Baikal in Siberia (Russia). Whole-rock samples and pure mineral separates from nine xenoliths have been analyzed for Sr and Nd isotopes in order to characterize the upper mantle beneath the southern Baikal rift zone. In an Sr-Nd isotope diagram both dry and hydrous xenoliths from Bartoy plot at the junction between the fields of MORB and ocean island basalts. This contrasts with data available on two other localities around Lake Baikal (Tariat and Vitim) where peridotites typically have Sr–Nd isotope compositions indicative of strong long-term depletion in incompatible elements. Our data indicate significant chemical and isotopic heterogeneity in the mantle beneath Bartoy that may be attributed to its position close to an ancient suture zone separating the Siberian Platform from the Mongol-Okhotsk mobile belt and occupied now by the Baikal rift. Two peridotites have clinopyroxenes depleted in light rare earth elements (LREE) with Sr and Nd model ages of about 2 Ga and seem to retain the trace element and isotopic signatures of old depleted lithospheric mantle, while all other xenoliths show different degrees of LREE-enrichment. Amphiboles and clinopyroxenes in the hydrous peridotites are in Sr–Nd isotopic disequilibrium. If this reflects in situ decay of ¹⁴⁷Sm and ⁸⁷Rb rather than heterogeneities produced by recent metasomatic formation of amphiboles then 300–400 Ma have passed since the minerals were last in equilibrium. This age range then indicates an old enrichment episode or repeated events during the Paleozoic in the lithospheric mantle initially depleted maybe 2 Ga ago. The Bartoy hydrous and enriched dry peridotites, therefore, are unlikely to represent fragments of a young asthenospheric bulge which, according to seismic reflection studies, reached the Moho at the axis of the Baikal rift zone a few Ma ago. By contrast, hydrous veins in peridotites may be associated with rift formation processes.     

Isotope geochemistry of Jeongok basalts,northernmost South Korea: Implications for the enriched mantle end-member component

South Korea separates two mantle source domains for Late Cenozoic intraplate volcanism in East Asia: depleted mid-ocean-ridge basalt (MORB) mantle-enriched mantle type 1 (DMM-EM1) in the north and DMM-EM2 in the south. We determined geochemical compositions, including Sr, Nd, Pb, and Hf isotopes for the Jeongok trachybasalts (∼0.51 to 0.15 Ma K–Ar ages) from northernmost South Korea, to better constrain the origin and distribution of the enriched mantle components. The Jeongok basalts exhibit light rare earth element (LREE)-enriched patterns ([La/Yb]_N = 9.2–11.6). The (La/Yb)_N ratios are lower than that of typical oceanic island basalt (OIB). On a primitive mantle-normalized incompatible element plot, the Jeongok samples show OIB-like enrichment in highly incompatible elements. However, they are depleted in moderately incompatible elements (e.g., La, Nd, Zr, Hf, etc.) compared with the OIB and exhibit positive anomalies in K and Pb. These anomalies are also prime characteristics of the Wudalianchi basalts, extreme EM1 end-member volcanics in northeast China. We have compared the geochemistry of the Jeongok basalts with those of available Late Cenozoic intraplate volcanic rocks from East Asia (from north to south, Wudalianchi, Mt. Baekdu and Baengnyeong for DMM-EM1, and Jeju for DMM-EM2). The mantle source for the Jeongok volcanics contains an EM1 component. The contribution of the EM1 component to East Asian volcanism increases toward the north, from Baengnyeong through Jeongok to Mt. Baekdu and finally to Wudalianchi. Modeling of trace element data suggests that the Jeongok basalts may have been generated by mixing of a Wudalianchi-like melt (EM1 end-member) and a melt that originated from a depleted mantle source, with some addition of the lithospheric mantle beneath the Jeongok area. In Nd–Hf isotope space, the most enriched EM1-component-bearing Jeongok sample shows elevation of ¹⁷⁶Hf/¹⁷⁷Hf at a given ¹⁴³Nd/¹⁴⁴Nd compared with OIB. Recycled pelagic sediments may explain the EM1-end-member component of northeastern Asian volcanism, possibly from the mantle transition zone.     

西藏西南部休古嘎布蛇绿岩的成因:岩石学和地球化学证据

休古嘎布蛇绿岩块位于雅鲁藏布缝合带(YZSZ)西段,主要由地幔橄榄岩和侵入其中的基性岩墙所组成。基性岩墙具有弧后盆地地球化学亲缘性,其LREE亏损,(La/Yb)N为0.39~0.55;具有明显的Nb、Ti负异常及Sr、Ba正异常。Sr、Nd同位素特征表明它们起源于亏损地幔,并且受到了板片析出流体的影响。4个基性岩墙的Sm-Nd同位素样品获得内部等时线年龄为126.2±9.1Ma(MSWD=0.44)。地幔橄榄岩具有汤勺形和U形两组REE分布型式,显示出不同程度部分熔融和地幔交代作用的特征,具有弧-盆体系地球化学亲缘性。第一组橄榄岩的LREE弱富集或近于平坦,尖晶石的Cr#值低而且变化不大,部分熔融程度较低(15%~20%),可能形成于弧后扩张盆地;第二组橄榄岩的LREE明显富集,尖晶石的Cr#值高而且变化较大(0.4~0.77),部分熔融程度较高(25%~30%),并经历了强烈的交代富集作用,可能与洋内岛弧有关。     

The Finero phlogopite-peridotite massif: an example of subduction-related metasomatism

The Finero peridotite massif is a harzburgite that suffered a dramatic metasomatic enrichment resulting in the pervasive presence of amphibole and phlogopite and in the sporadic occurrence of apatite and carbonate (dolomite)-bearing domains. Pyroxenite (websterite) dykes also contain phlogopite and amphibole, but are rare. Peridotite bulk-rock composition retained highly depleted major element characteristics, but was enriched in K, Rb, Ba, Sr, LREE (light rare earth elements) (La_N/Yb_N = 8–17) and depleted in Nb. It has high radiogenic Sr (⁸⁷Sr/⁸⁶Sr₍₂₇₀₎ = 0.7055–0.7093), low radiogenic Nd (ɛNd₍₂₇₀₎= −1 to −3) and EMII-like Pb isotopes. Two pyroxenite – peridotite sections examined in detail show the virtual absence of major and trace element gradients in the mineral phases. In both rock types, pyroxenes and olivines have the most unfertile major element composition observed in Ivrea peridotites, spinels are the richest in Cr, and amphibole is pargasite. Clinopyroxenes exhibit LREE-enriched patterns (La_N/Yb_N ∼16), negative Ti and Zr and generally positive Sr anomaly. Amphibole has similar characteristics, except a weak negative Sr anomaly, but incompatible element concentration ∼1.9 (Sr) to ∼7.9 (Ti) times higher than that of coexisting clinopyroxene. Marked geochemical gradients occur toward apatite and carbonate-bearing domains which are randomly distributed in both the sections examined. In these regions, pyroxenes and amphibole (edenite) are lower in mg## and higher in Na₂O, and spinels and phlogopite are richer in Cr₂O₃. Both the mineral assemblage and the incompatible trace element characteristics of the mineral phases recall the typical signatures of “carbonatite” metasomatism (HFSE depletion, Sr, LILE and LREE enrichment). Clinopyroxene has higher REE and Sr concentrations than amphibole (^amph/cpxD_REE,Sr = 0.7–0.9) and lower Ti and Zr concentrations. It is proposed that the petrographic and geochemical features observed at Finero are consistent with a subduction environment. The lack of chemical gradients between pyroxenite and peridotite is explained by a model where melts derived from an eclogite-facies slab infiltrate the overhanging harzburgitic mantle wedge and, because of the special thermal structure of subduction zones, become heated to the temperature of the peridotite. If the resulting temperature is above that of the incipient melting of the hydrous peridotite system, the slab-derived melt equilibrates with the harzburgite and a crystal mush consisting of harzburgite and a silica saturated, hydrous melt is formed. During cooling, the crystal mush crystallizes producing the observed sequence of mineral phases and their observed chemical characteristics. In this context pyroxenites are regions of higher concentration of the melt in equilibrium with the harzburgite and not passage-ways through which exotic melts percolated. Only negligible chemical gradients can appear as an effect of the crystallization process, which also accounts for the high amphibole/clinopyroxene incompatible trace element ratios. The major element refractory composition is explained by an initially high peridotite/melt ratio. The apatite, carbonate-bearing domains are the result of the presence of some CO₂ in the slab-derived melt. The CO₂/H₂O ratio in the peridotite mush increased by crystallization of hydrous phases (amphibole and phlogopite) locally resulting in the unmixing of a late carbonate fluid. The proposed scenario is consistent with subduction of probably Variscan age and with the occurrence of modal metasomatism before peridotite incorporation in the crust. Received: 20 July 1998 / Accepted: 28 October 1998     

Paleoproterozoic subduction-related metasomatic signatures in the lithospheric mantle beneath NE Brazil: inferences from trace element and Sr–Nd–Pb isotopic compositions of Neoproterozoic high-K igneous rocks

Late Neoproterozoic (ca. 580 Ma), high-K, mafic-intermediate rocks represent voluminous bimodal magmatism in the Borborema Province, northeast Brazil. These rocks show the following chemical signatures that reflect derivation from a subduction-modified lithospheric mantle source: (1) enrichment in large ion lithophile elements (Rb, Ba, K, Th) and light rare-earth elements (REE) (La/Yb_CN=11–70), (2) pronounced negative Nb anomalies, and (3) radiogenic Sr (0.71202–0.7059) and unradiogenic Nd (_Nd from −9.3–−20.1) isotopic compositions. T_DM model ages suggest that modification of the lithospheric mantle source (metasomatised garnet lherzolite) may have occurred in the Paleoproterozoic during the Transamazonian/Eburnean tectonics that affected the region. Interaction with asthenospheric fluids is believed to have partially melted this enriched source in the Neoproterozoic, probably as a result of asthenosphere-derived fluid percolation in the Brasiliano/Pan-African shear zones that controlled the emplacement of these mafic-intermediate magmas. The involvement of this asthenospheric component is supported by the nonradiogenic Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb=16–17.3, ²⁰⁷Pb/²⁰⁴Pb=15.1–15.6, ²⁰⁸Pb/²⁰⁴Pb=36–37.5), which contrast with the enriched Sr and Nd compositions and thereby suggest the decoupling of Rb–Sr, Sm–Nd, and U–Pb systems at the time of intrusion of the mafic-intermediate magmas in the crust.     

Subsolidus reactions monitored by trace element partitioning: the spinel- to plagioclase-facies transition in mantle peridotites

Mantle peridotites of the External Liguride (EL) Units (Northern Apennines) mainly consist of fertile spinel-lherzolites partially recrystallized to plagioclase-facies assemblages, and are consequently appropriate to investigate the interphase element partitioning related to the transition from spinel- to plagioclase-facies stability field. Evidence for the development of the plagioclase-facies assemblage is mainly given by: (1) large exsolution lamellae of orthopyroxene and plagioclase within spinel-facies clinopyroxene; (2) plagioclase rims around spinel; (3) granoblastic domains made up of olivine+plagioclase±clino-and orthopyroxene. In situ major and trace [REE (rare-earth elements), Ti, Sc, V, Cr, Sr, Y, Zr and Ba] element mineral analyses have been performed, by electron and ion probe, on selected samples which show the progressive development of the plagioclase-bearing assemblage. The main compositional variations observed during the change from spinel- to plagioclase-facies minerals are as follows: (1) clinopyroxenes decrease in Al, Na, Sr, Eu/Eu^* and increase in Y, V, Sc, Cr, Zr and Ti; (2) amphiboles decrease in Eu/Eu^*, Sr, Ba and increase in Zr and V; (3) spinels decrease in Al and increase in Cr and Ti. The most striking feature is the decoupling in the behaviour of similarly incompatible elements (D about 0.1) in clinopyroxene, e.g. Sr decrease is mirrored by Zr increase. Massbalance calculations indicate that the trace element interphase redistribution documented in the EL peridotites occurred in a closed system and in response to the metamorphic reaction governing the transition from the spinel- to the plagioclase-facies stability field. The observed element partitioning reveals, moreover, that subsolidus re-equilibration processes in the upper mantle produce HFSE (high-field-strength element)/REE fractionation in minerals, which must be evaluated for a reliable determination of mineral-melt distribution coefficients. The results of this study furnish evidence for subsolidus metamorphic evolution during decompression, without concomitant partial melting processes. This is consistent with the interpretation that the EL peridotites represent subcontinental lithospheric mantle emplaced at the surface in response to lithospheric thinning and tectonic denudation mechanisms related to the Triassic-Jurassic rifting of the Ligure-Piedmontese basin.