Asthenospheric and lithospheric sources for Mesozoic dolerites from Liberia (Africa): trace element and isotopic evidence

Combined elemental, and Sr and Nd isotopic data are presented for Mesozoic dolerite dikes of Liberia (Africa) which are related to the initial stage of opening of the Atlantic Ocean.The large scatter of both trace element and isotopic data allows the identification of five groups of dolerites which cannot be related to each other by simple processes of mineral fractionation from a common source. On the contrary, the observed chemical and isotopic variation within some dolerites (Groups I and II) may result either from variable degrees of melting of an isotopically heterogeneous source or mixing between enriched and depleted oceanic type mantle. For the other dolerites (Groups III–V) mixing with a third mantle source with more radiogenic Sr and with element ratios characteristic of subduction environments is suggested. This third source is probably the subcontinental lithospheric mantle.Finally, no significant modification by interaction with continental crust is apparent in most of the analyzed samples.     

Trace element geochemistry of some continental tholeiites

Continental tholeiites from four regions (Late Cretaceous to Early Eocene Deccan Trap lavas of central India, Early Mesozoic tholeiites from the Atlantic margins of Northwest Africa-Morocco, and northeastern North America-Nova Scotia, Canada and Precambrian Coppermine River basalts from Northwest Territories, Canada) differ from MORB by higher concentrations of K, Rb, Ba and Th and to a lesser degree light REE. Their chondrite-normalized trace element patterns show negative Nb anomalies. The distribution and variation of trace elements indicate that the rocks from all the areas studied were affected by interaction with the continental crust. It is suggested that continental tholeiites have been generated from a similar source as oceanic tholeiites and many of their geochemical differences are related to crustal contamination.     

Plate-plume-accretion tectonics in Proterozoic terrain of northeastern Rajasthan, India: Evidence from mafic volcanic rocks of north Delhi fold belt

Abstract   The northern part of the Aravalli mountain belt of northwestern Indian shield is broadly composed of three Proterozoic volcano-sedimentary domains, i.e. the Bayana, the Alwar and the Khetri basins, comprising collectively the north Delhi fold belt. Major, trace and rare earth element concentrations of mafic volcanic rocks of the three basins exhibit considerable diversity. Bayana and Alwar volcanics are typical tholeiites showing close similarity with low Ti–continental flood basalts (CFB) with the difference that the former shows enriched and the latter flat incompatible trace element and rare earth element (REE) patterns. However, the Khetri volcanics exhibit a transitional composition between tholeiite and calc-alkaline basalts. It appears that the melts of Bayana and Alwar tholeiites were generated by partial melting of a common source within the spinel stability field possibly in the presence of mantle plume. During ascent to the surface the Bayana tholeiites suffered crustal contamination but the Alwar tholeiites erupted unaffected. Geochemically, the Khetri volcanics are arc-like basalts which were generated in a segment of mantle overlying a Proterozoic subduction zone. It is suggested that at about 1800 Ma the continental lithosphere in northeastern Rajasthan stretched, attenuated and fractured in response to a rising plume. The produced rifts have undergone variable degrees of crustal extension. The extension and attenuation of the crust facilitated shallowing of the asthenosphere which suffered variable degree of melting to produce tholeiitic melts – different batches of which underwent different degrees of lithospheric contamination depending upon the thickness of the crust in different rifted basins. The occurrence of subduction-related basaltic rocks of Khetri Belt suggests that a basin on the western margin of the craton developed into a mature oceanic basin.     

Origin of basalts from the Marquesas Archipelago (south central Pacific Ocean): isotope and trace element constraints

Basalts from the Marquesas Archipelago display significant variations according to magmatic type in ¹⁴³Nd/¹⁴⁴Nd (0.512710–0.512925) and ⁸⁷Sr/⁸⁶Sr (0.70288–0.70561) suggesting heterogeneities at various scales in the mantle source, with respectively the highest and lowest values in tholeiites compared to alkali basalts. This relationship is the reverse from that observed in the Hawaiian islands. Systematic indications of magma mixing are recognized from the relationships between trace element and isotopic ratios. Tholeiites from Ua Pou Island which have unradiogenic Sr (about 0.7028) plot close to basalts from Tubuai and St. Helena, i.e. distinctly below the main mantle trend in the Nd vs. Sr isotopic diagram. It is suggested that the source of these tholeiites is ancient subducted lithosphere which has suffered previous extraction of liquid with island arc tholeiite composition. The trace element and isotopic data of the basalts from the other Marquesas Islands imply the contamination of an equivalent source by an enriched component. This latter has trace element characteristics of the upper crust.     

Lithophile elements in Huronian low-Ti continental tholeiites from Canada, and evolution of the Precambrian mantle

Huronian basalts from central Ontario, Canada, dated at about 2450 Ma and associated with an early rifting episode, are classified as siliceous, low-TiNb tholeiites. They display strong enrichment in large-ion lithophile (LILE) and light rare earth (LREE) elements compared to modern oceanic lavas. The tectonic setting and geochemistry resemble Mesozoic rift-related low-Ti flood basalts, including the Ferrar Group of Antarctica, and the Parana and equivalent Etendeka volcanics of south Brazil and Namibia, respectively. High LILE/LREE ratios are also similar to subduction-related island arc tholeiites, and it is suggested that enrichment of the Huronian lithospheric mantle source occurred through ancient subduction of crustal material, probably during formation and consolidation of the Archean continental crust.Melting models suggest that Huronian subcontinental mantle source compositions, derived from least contaminated, aphyric, mafic end-members, had already undergone a complex evolution, including withdrawal of Archean basalts and hydrous enrichment in incompatible components. Despite several subsequent melting episodes and a second, probably magmatic, enrichment event, however, many aspects of the Huronian source signature were preserved, and appeared in later basaltic products of this mantle mass. Keweenawan volcanics, for example, dated at about 1100 Ma, preserve low P, Zr, Ti and HREE abundances.     

Major- and trace-element systematics and isotope geochemistry of Cenozoic mafic volcanic rocks from the Vogelsberg (central Germany): Constraints on the origin of continental alkaline and tholeiitic basalts and their mantle sources

The Cenozoic basaltic province of the Vogelsberg area (central Germany) is mainly composed of intercalated olivine to quartz tholeiites and near-primary nephelinites to basanites. The inferred mantle source for the alkaline and tholeiitic rocks is asthenospheric metasomatized garnet peridotite containing some amphibole as the main hydrous phase. Trace element modelling indicates 2 to 3% partial melting for the alkaline rocks and 5 to 7% partial melting for the olivine tholeiites. Incompatible trace element abundances and ratios as well as Nd and Sr radiogenic isotope compositions lie between plume compositions and enriched mantle compositions and are similar to those measured in Ocean Island Basalts (OIB) and the Central European Volcanic Province elsewhere. The mafic olivine tholeiites have similar Ba/Nb, Ba/La and Nd–Sr isotope ratios to the alkaline rocks indicating derivation of both magma types from chemically comparable mantle sources. However, Zr/Nb ratios are slightly higher in olivine tholeiites than in basanites reflecting some fractionation of Zr relative to Nb during partial melting. Quartz tholeiites have higher Ba/Nb, Zr/Nb, La/Nb, but lower Ce/Pb ratios and lower Nd isotope compositions than the alkaline rocks which can be explained by interaction of the basaltic melt with lower (granulite facies) crustal material or partial melts thereof during stagnation within the lower crust. It appears most likely that upwelling of hot, asthenospheric material results in the generation of primitive alkaline rocks at the base of the lithosphere at depths of 75–90 km. Lithospheric extension together with minor plume activity and probably lower lithosphere erosion induced melting of shallower heterogenous upper mantle generating a spectrum of olivine tholeiitic melts. These olivine tholeiitic rocks evolved via crystal fractionation and probably limited contamination to quartz tholeiites.     

Origin of Icelandic basalts: A review of their petrology and geochemistry

The petrology and geochemistry of Icelandic basalts have been studied for more than a century. The results reveal that the Holocene basalts belong to three magma series: two sub-alkaline series (tholeiitic and transitional alkaline) and an alkali one. The alkali and the transitional basalts, which occupy the off-rift volcanic zones, are enriched in incompatible trace elements compared to the tholeiites, and have more radiogenic Sr, Pb and He isotope compositions. Compared to the tholeiites, they are most likely formed by partial melting of a lithologically heterogeneous mantle with higher proportions of melts derived from recycled oceanic crust in the form of garnet pyroxenites compared to the tholeiites. The tholeiitic basalts characterise the mid-Atlantic rift zone that transects the island, and their most enriched compositions and highest primordial (least radiogenic) He isotope signature are observed close to the centre of the presumed mantle plume. High-MgO basalts are found scattered along the rift zone and probably represent partial melting of refractory mantle already depleted of initial water-rich melts. Higher mantle temperature in the centre of the Iceland mantle plume explains the combination of higher magma productivity and diluted signatures of garnet pyroxenites in basalts from Central Iceland. A crustal component, derived from altered basalts, is evident in evolved tholeiites and indeed in most basalts; however, distinguishing between contamination by the present hydrothermally altered crust, and melting of recycled oceanic crust, remains non-trivial. Constraints from radiogenic isotope ratios suggest the presence of three principal mantle components beneath Iceland: a depleted upper mantle source, enriched mantle plume, and recycled oceanic crust.The study of glass inclusions in primitive phenocrysts is still in its infancy but already shows results unattainable by other methods. Such studies reveal the existence of mantle melts with highly variable compositions, such as calcium-rich melts and a low-¹⁸O mantle component, probably recycled oceanic crust. Future high-resolution seismic studies may help to identify and reveal the relative proportions of different lithologies in the mantle.     

A major change in magma sources in late Mesozoic active margin of the circum-Sea of Japan domain: Geochemical constraints from late Paleozoic to Paleogene mafic dykes in the Sergeevka belt,southern Primorye,Russia

More than 30 mafic dykes crop out in the Sergeevka belt in the coastal South Primorye, Far East Russia, of which geologic settings have been unclear for years. This study conducted major- and trace elements characterization, Sr–Nd isotope analyses, and Ar–Ar amphibole and U–Pb zircon datings for these rocks in order to identify their origin. The results demonstrated that all dykes are characterized by high Ba/Yb and low Nb/Y, Zr/Y, and Th/Yb ratios, which suggest their origin from arc melts derived from thin wedge mantle and shallow-dipping slab. These dykes are clearly separated into two distinct age/geochemistry suites; that is, the Paleogene and Early Cretaceous one with dolerites/basalts and adakitic rocks, and the Permian–Triassic one with high-Mg and high-Al gabbro-dolerite varieties. Their geochemistry suggests that the older suite was sourced from a primitive depleted MORB mantle (DMM)-type mantle, whereas the younger suite from an enriched mantle II (EM2)-type mantle domain. The transition in source type from DMM to EM2 occurred during the Jurassic-earliest Cretaceous time, probably by a strong influence of a mantle plume onto the long-continuing subduction-related magmatism. The plume influence reached the maximum when the unique meimechite-picrite complex formed in the region.     

The Karoo igneous province — A problem area for inferring tectonic setting from basalt geochemistry

Tholeiitic basalts and associated intrusives are the major component of the Karoo igneous province. They are of Mesozoic age and constitute one of the world's classic continental flood basalt (CFB) provinces. It has been argued that most Karoo basalts have not undergone significant contamination with continental crust and that their lithospheric mantle source areas were enriched in incompatible minor and trace elements during the Proterozoic. The only exceptions to this are late-stage MORB-like dolerites near the present-day continental margins which are considered to be of asthenospheric origin.When data for the “southern” Karoo basalts are plotted on many of the geochemical discriminant diagrams which have been used to infer tectonic setting, essentially all of them would be classified as calc-alkali basalts (CAB's) or low-K tholeiites. Virtually none of them plot in the compositional fields designated as characteristic of “within-plate” basalts. There is little likelihood that the compositions of the Karoo basalts can be controlled by active subduction at the time of their eruption and no convincing evidence that a “subduction component” has been added to the subcontinental lithospheric mantle under the entire area in which the basalts crop out. It must be concluded that the mantle source areas for CAB's and the southern Karoo basalts have marked similarities.In contrast, the data for “northern” Karoo basalts largely plot in the “within-plate” field on geochemical discriminant diagrams. Available data suggest that the source composition and/or the restite mineralogy and degree of partial melting are different for southern and northern Karoo basalts. There is no evidence for any difference in tectonic setting between the southern and northern Karoo basalts at the time they were erupted. This appears to be clear evidence that specific mantle source characteristics and/or magmatic processes can vary within a single CFB province to an extent that renders at least some geochemical discriminant diagrams most unreliable for classifying tectonic environment with respect to continental volcanic rocks.     

An outline of the geology and geochemistry,and the possible petrogenetic evolution of the volcanic rocks of the Tonga-Kermadec-New Zealand island arc

The Pleistocene-Recent volcanism of this arc extends nearly linearly NNE from northern New Zealand for some 2800 km. Along its western margin lies an active marginal basin (Lau Basin and Havre Trough) which has its southern termination in the Taupo volcanic zone (TVZ, New Zealand). The New Zealand arc segment is developed within a continental crust, whereas the Tonga-Kermadec segments are developed on a ridge system within the oceanic basin. Submarine morphology suggests that the Kermadec volcanoes represent a less advanced stage of evolution relative to those of Tonga.Magmas erupted within the TVZ are dominantly rhyolitic (≈16,000 km³) with subordinate andesites and rare high-alumina tholeiites and dacites. The Kermadec Islands are dominated by tholeiites and basaltic andesites, with subordinate andesites and dacites. The Tongan Islands are dominated by basaltic andesites, with locally developed andesites and dacites. These Tonga-Kermadec lavas are characterised by subcalcic groundmass clinopyroxenes, whereas the younger group of TVZ andesites contain groundmass hypersthene and augite.Geochemically, the TVZ andesites are systematically enriched (relative to those of Tonga-Kermadec) in “incompatible” elements (e.g. K, Rb, Cs, Ba, light REE, U, Th, Zr, Pb), are less Fe-enriched, and contain more radiogenic Sr and Pb (excepting certain ²⁰⁷Pb/²⁰⁴Pb compositions). The evidence points to crustal equilibration of the TVZ andesites prior to eruption.A complete overlap of major and trace element chemistry (including TiO₂) is observed between the Kermadec-TVZ tholeiites and basaltic andesites, and the ocean floor tholeiites of the Lau Basin. Compared to the Tongan lavas, those of the Kermadecs exhibit a greater degree of chemical variability, also reflected in the greater heterogeneity in their Pb isotopic compositions. Moreover, many of the Tonga-Kermadec basaltic andesites exhibit more depleted “incompatible” trace element abundances than the Kermadec and TVZ tholeiites.The “primary” magmas of this arc are interpreted to be of basaltic andesite type, derived from Benioff zone melting (essentially anhydrous), but extensively modified by low-pressure crystal fractionation processes. The Kermadec tholeiites are explained as products of relatively shallow upper mantle partial fusion induced during the earlier stages of diapiric rise of Benioff zone-derived magmas, which are sufficiently hot to intersect the peridotite solidus. This should result in the production and intermixing of a series of magmas extending from olivine tholeiite to basaltic andesite composition. The voluminous rhyolites of TVZ are interpreted as the products of crustal fusion involving Mesozoic sediments.     

Basalt geochemistry and tectonic discrimination within continental flood basalt provinces

Continental flood basalts are usually regarded as a single tectonomagmatic entity but frequently quoted examples exhibit a variety of tectonic settings. In one well-studied, classic, flood basalt province, the Mesozoic Karoo province of southern Africa, magmatism occurred in the following tectonic settings: (a) continental rifting leading to ocean-floor spreading in the South Atlantic Ocean (Etendeka suite of Namibia); (b) stretched continental lithosphere and rifting not leading directly to ocean-floor formation (Lebombo suite of southeastern Africa); and (c) an a-tectonic, within-plate, continental setting characterized by an absence of faulting or warping (Lesotho highlands and Karoo dolerites of South Africa). By means of spidergrams of the elements Rb, Ba, Th, Nb, K, La, Ce, Sr, Nd, P, Hf, Zr, Sm, Ti, Tb, Y, V, Ni and Cr, uncontaminated tholeiites from (c) above [i.e. the Lesotho-type continental flood basalts (LTCFB)] are compared with mid-ocean ridge basalts (MORB), ocean-island tholeiites (OIT), and tholeiites and calc-alkali basalts from subduction environments. The comparison reveals the LTCFBs are geochemically distinct. The differences are reflected in relative enrichments or depletions of the more incompatible elements (Rb-Ce) to less incompatible elements (Ce-Y), i.e. the overall slope of the spidergrams, and in anomalous enrichments or depletions of one or more of the elements Th, K, Nb, Sr, Ti, Hf, and Zr. The distinctive geochemical character of the Lesotho LTCFBs is interpreted in terms of a lithospheric mantle source for the basalts. This is supported by isotopic data. There are no major geochemical differences between Lesotho CFBs and basalts of the rift-related Etendeka and Lebombo suites, although the latter are somewhat enriched in Rb, Ba and K. However, unlike the Lesotho basalts, the Lebombo and Etendeka basalts are associated with voluminous silicic volcanics or intrusive centres and late-stage dolerites having MORB/OIT (i.e. asthenospheric) geochemical characteristics. The flood basalt/silicic magmatism/late-stage dyke swarm association is characteristic of several rift or thinned lithosphere environments (e.g., Ethiopia, Skye, eastern Greenland) but in many of these the flood basalts have ocean-island basalt (OIT) geochemical characteristics. The Lesotho-type CFB geochemistry is exhibited by the Grande Ronde Basalt of the Columbia River Group (a possible subduction-related flood basalt province) and the basic rocks associated with Mesozoic rifting in the North and South Atlantic. Basalt geochemistry alone is unhelpful in determining the tectonic setting of CFBs although the rift-related environments may be identified by the petrology and geochemistry of the whole igneous suite. A two-source model is proposed for the mantle-derived basic rocks in rift-related CFB provinces. Early enriched basalts are derived from the lithosphere and, following pronounced lithospheric attenuation or rifting, later MORB-like melts are emplaced from the rising asthenosphere. The presence of both Lesotho- and OIT-type geochemical patterns in rift-related CFBs suggests that the lithosphere exhibits different styles of enrichment.     

Isotope and trace element geochemistry of young Pacific seamounts: implications for the scale of upper mantle heterogeneity

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

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

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

Development of continental lithospheric mantle as reflected in the chemistry of the Mesozoic Appalachian Tholeiites, U.S.A.

Geochemical analyses of dikes, sills, and volcanic rocks of the Mesozoic Appalachian Tholeiite (MAT) Province of the easternmost United States provide evidence that continental tholeiites are derived from continental lithospheric mantle sources that are genetically and geochronologically related to the overlying continental crust. Nineteen olivine tholeiites and sixteen quartz tholeiites from the length of this province, associated in space and time with the last opening of the Atlantic, display significant isotopic heterogeneity: initial ε_Nd = +3.8 to −5.7; initial ⁸⁷Sr/⁸⁶Sr= 0.7044−0.7072; ²⁰⁶Pb/²⁰⁴Pb= 17.49−19.14; ²⁰⁷Pb/²⁰⁴Pb= 15.55−15.65; ²⁰⁸Pb/²⁰⁴Pb= 37.24−39.11. In PbPb space, the MAT define a linear array displaced above the field for MORB and thus resemble oceanic basalts with DUPAL Pb isotopic traits. A regression of this array yields a secondary PbPb isochron age of ≈ 1000 Ma (μ₁ = 8.26), similar to Sm/Nd isochrons from the southern half of the province and to the radiometric age of the Grenville crust underlying easternmost North America. The MAT exhibit significant trace element ratio heterogeneity (e.g., Sm/Nd= 0.226−0.327) and have trace element traits similar to convergent margin magmas [e.g., depletions of Nb and Ti relative to the rare earth elements on normalized trace element incompatibility diagrams, Ba/Nb ratios (19–75) that are significantly greater than those of MORB, and low TiO₂ (0.39–0.69%)].Geochemical and geological considerations very strongly suggest that the MAT were not significantly contaminated during ascent through the continental crust. Further, isotope and trace element variations are not consistent with the involvement of contemporaneous MORB or OIB components. Rather, the materials that control the MAT incompatible element chemistry were derived from subcontinental lithospheric mantle. Thus: (1) the MAT/arc magma trace element similarities; (2) the PbPb and Sm/Nd isochron ages; and (3) the need for a method of introducing an ancient (> 2−3 Ga) Pb component into subcontinental mantle that cannot be much older than 1 Ga leads to a model whereby the MAT were generated by the melting of sediment-contaminated arc mantle that was incorporated into the continental lithosphere during arc activity preceding the Grenville Orogeny (≈ 1000 Ma).     

Intracratonic asthenosphere upwelling and lithosphere rejuvenation beneath the Hoggar swell (Algeria): Evidence from HIMU metasomatised lherzolite mantle xenoliths

The mantle xenoliths included in Quaternary alkaline volcanics from the Manzaz-district (Central Hoggar) are proto-granular, anhydrous spinel lherzolites. Major and trace element analyses on bulk rocks and constituent mineral phases show that the primary compositions are widely overprinted by metasomatic processes. Trace element modelling of the metasomatised clinopyroxenes allows the inference that the metasomatic agents that enriched the lithospheric mantle were highly alkaline carbonate-rich melts such as nephelinites/melilitites (or as extreme silico-carbonatites). These metasomatic agents were characterized by a clear HIMU Sr–Nd–Pb isotopic signature, whereas there is no evidence of EM1 components recorded by the Hoggar Oligocene tholeiitic basalts. This can be interpreted as being due to replacement of the older cratonic lithospheric mantle, from which tholeiites generated, by asthenospheric upwelling dominated by the presence of an HIMU signature. Accordingly, this rejuvenated lithosphere (accreted asthenosphere without any EM influence), may represent an appropriate mantle section from which deep alkaline basic melts could have been generated and shallower mantle xenoliths sampled, respectively. The available data on lherzolite xenoliths and alkaline lavas (including He isotopes, Ra < 9) indicate that there is no requirement for a deep plume anchored in the lower mantle, and that sources in the upper mantle may satisfactorily account for all the geochemical/petrological/geophysical evidence that characterizes the Hoggar swell. Therefore the Hoggar volcanism, as well as other volcanic occurrences in the Saharan belt, are likely to be related to passive asthenospheric mantle uprising and decompression melting linked to tensional stresses in the lithosphere during Cenozoic reactivation and rifting of the Pan–African basement. This can be considered a far-field foreland reaction of the Africa–Europe collisional system since the Eocene.     

Deccan plume,lithosphere rifting,and volcanism in Kutch,India

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.     

U&z.sbnd;Th isotopic systematics at 13°N east Pacific Ridge segment

Fresh basaltic glasses have been analyzed for U&z.sbnd;Th disequilibrium systematics as part of an extensive study on the East Pacific Rise (EPR) at 12°45′N. These samples are well described in terms of major and trace elements as well as in Nd, Pb and Sr isotopes. Our results show significant heterogeneities in the mantle source at a small scale, and show heterogeneities at larger scales also when compared to other EPR data.U and Th concentration and isotopic data rule out fractional crystallization as a main process and support a mixing model in agreement with the marble cake model developed by Alle`gre and Turcotte and constrained by trace elements and Nd, Sr and Pb isotopes on the same samples by Prinzhofer et al.Based on the high ( ²³⁰Th/²³²Th ) isotopic ratios on recent tholeiites especially the Th/U values inferred for their sources clearly show that the upper mantle Th/U has decreased with time.     

Petrochemistry and geochemistry of HP metabasites from Haiyangsuo in Sulu UHP belt of eastern China

Abundant metabasites occur in highly deformed granitic and migmatitic gneisses as blocks and lenses of tens of meter size around the Haiyangsuo area, northeast part of Sulu UHP belt, eastern China. They comprise garnet-pyroxene granulites, eclogitized granulites and amphibolites. Their protolith compositions were mainly olivine tholeiite and quartz tholeiite, and show variation from Mg-rich to Fe-rich component as tholeiitic cumulates. Pearce’s element ratio slopes suggested that protolith of these rocks were comagmatic, and generated from a primary magma by fractional crystallization of plagioclase, olivine and clinopyroxene. The crystallization differentiation has also been evidenced by trace elements, such as parallel REE patterns, Ni vs Ce variations, Sr increasing depletions, although the large ion lithophile elements (LILE) were modified to different extent during metamorphism. Trace element composition and Nd isotopes indicate a depleted mantle origin for these rocks. But they are not likely to be fragments of ophiolites or tholeiites connected with subduction, they formed probably at intra-continent environment. Sm-Nd whole rock isochron age of 2252±180Ma indicates approximately the formation age of igneous protolith of these rocks, almost 2000Ma earlier than the formation of the Dabie-Sulu UHP collision zone at about 240–220 Ma.     

Causes of spatial compositional variations in Mariana arc lavas: Trace element evidence

New inductively coupled plasma mass spectrometry (ICP-MS) trace element data are presented on a suite of arc lavas from the northern Mariana and southern Bonin island arcs. The samples were dredged from seamounts in the Central Island Province (CIP), the Northern Seamount Province (NSP) and the Volcano Arc (VA), and they range in composition from low-K tholeiites to shoshonites. Previous studies on these samples concluded that the primary compositional control was two-component mixing between a fluid-metasomatized mid-ocean ridge basalt (MORB) source and an enriched, ocean island basalt (OIB)-like, mantle component, with subducted sediment material playing a secondary role. However, the new trace element data suggest that the compositional variations along the Mariana arc can be better explained by the addition of spatially varying subduction components to a spatially varying mantle source. The data suggest that the subduction component in the CIP and VA is dominated by aqueous fluids derived from altered oceanic crust and a pelagic sediment component, while the subduction component in the NSP is dominated by more silicic fluids derived from volcanogenic sediments as well as from pelagic sediment and altered oceanic crust. The mantle wedge in the CIP and VA is depleted relative to a normal mid-ocean ridge basalt source by loss of a small melt fraction, while the mantle wedge in the NSP is enriched either by possible gain of a small melt fraction or addition of a sediment-derived melt. Because the subduction of seamounts controls the arc and back-arc geometries, so the concomitant variation between subducted material and mantle composition may be no coincidence. The high field strength element (HFSE) data indicate a high degree of melting (∼ 25–30%) throughout the arc, ∼ 10% of which may be attributed to decompression and ∼ 20% to fluid addition.     

Petrology of basalts from Loihi Seamount,Hawaii

Loihi Seamount is the southeasternmost active volcano of the Emperor-Hawaii linear volcanic chain. It comprises a spectrum of basalt compositional varieties including basanite, alkali basalt, transitional basalt and tholeiite. Samples from four dredge collections made on Scripps Institution of Oceanography Benthic Expedition in October 1982 are tholeiite. The samples include highly vesicular, olivine-rich basalt and dense glass-rich pillow fragments containing olivine and augite phenocrysts. Both quartz-normative and olivine-normative tholeiites are present. Minor and trace element data indicate relatively high abundances of low partition coefficient elements (e.g., Ti, K, P. Rb, Ba, Zr) and suggest that the samples were derived by relatively small to moderate extent of partial melting, of an undepleted mantle source. Olivine composition, MgO, Cr and Ni abundances, and Mg/(Mg+Fe), are typical of moderately fractionated to relatively unfractionated “primary” magmas. The variations in chemistry between samples cannot be adequately explained by low-pressure fractional crystallization but can be satisfied by minor variations in extent of melting if a homogeneous source is postulated. Alternatively, a heterogeneous source with variable abundances of certain trace elements, or mixing of liquids, may have been involved. Data for ³He/⁴He, presented in a separate paper, implies a mantle plume origin for the helium composition of the Loihi samples. There is little variation in the helium isotope ratio for samples having different compositions and textures. The helium data are not distinctive enough to unequivocally separate the magma sources for the tholeiitic rocks from the other rock types such as Loihi alkalic basalts and the whole source region for Loihi may have a nearly uniform helium compositions even though other element abundances may be variable. Complex petrologic processes including variable melting, fractional crystallization and magma mixing may have blurred original helium isotopic signatures.     

Early Archaean rocks and geochemical evolution of the earth's crust

Remnants of Early Archaean rocks (>FX3000 m.y. old) are reported from most continents. A critical review of the radiometric data shows that few of these are well authenticated and most are very limited in extent. The oldest are predominantly plutonic gneisses of tonalitic-to-granitic composition (e.g., the basement gneisses of West Greenland, Labrador, Rhodesia and South Africa). In all cases there are inclusions of meta-volcanic and sedimentary rocks with greenstone belt affinities which probably represent crust into which the igneous parents of the gneisses were intruded.The trace element chemistry of these very old rocks is reviewed in an attempt to establish the mechanism of formation of early crust and place constraints on the chemical evolution of the earth's mantle. “Mantle-type” Sr isotope compositions show that the sialic members of both early gneisses and greenstone belts were not derived from much older crustal differentiates, either at 3800 or at 2800 m.y. ago. However, trace element ratios such as K/Rb and Sr/Ba, and rare earth element abundances, are not consistent with direct derivation of the plutonic suite from the upper mantle and also rule out a common parentage for the tonalites and granites. An origin by partial melting of metamorphosed juvenile crust with a composition range equivalent to that represented by the greenstone belts is preferred. Tonalites resulted from high-pressure melting of mafic garnet-amphibolite and at least some of the granites from low-pressure melting of more felsic (possibly even sedimentary) material.The trace element chemistry of the greenstone belt volcanics is thought to characterize the composition of early mantle melts, although the best preserved and best documented cases are about 500–1000 m.y. younger than the oldest known gneisses. The dominant type is tholeiite with low incompatible element contents and light-depleted or essentially flat rare earth patterns, features even more marked in the ultramafic komatiites which represent large degrees of melting. More evolved calc-alkaline rocks with relative incompatible and light rare earth element enrichment are also important. With the exception of the ultramafic lavas, all these types can be matched by the chemistry of present-day oceanic volcanism.It is concluded that the range of trace element variations in the earth's mantle was comparable in early Archaean times to that at the present. This is supported by mass balance calculations for the lithophile elements which have been preferentially extracted into the crust. Thus the isotope and trace element evidence of the oldest rocks argues against primary differentiation of the crust either during accretion of the earth or during its first 500 m.y. as a solid body. Crust formation has probably occurred continuously, although worldwide evidence for magmatism at around 2800 m.y. ago probably marks a particularly active period.