The Geochemistry and Experimental Petrology of Sodic Alkaline Basalts from Oatlands, Tasmania

Sodic basalts of Oligocene-Early Micene age occur within anEarly Tertiary graben in the Oatlands district of Tasmania.They include olivine tholeiites, alkali olivine basalts, basanites,transitional nephelinites, nepheline hawaiites, and nephelinemugearites. They have compositional characteristics in commonwith sodic alkaline basalt suites from other parts of the world.With decreasing SiO₂, concentrations of CaO, alkalis, P₂O₅,and incompatible trace elements increase. Compositional and experimental data for the basalts are consistentwith their derivation by polybaric partial melting of a garnetlherzolite source enriched in P₂O₅, light rare earths, Nb, andother incompatible trace elements. Experimental data for a primitivenepheline basanite from the Oatlands district indicate thatconcentrations of H₂O+CO₂ need not have been more than 6?5 wt.%for the original basanite magma to have derived from an amphibole-bearinggarnet lherzolite source. In the case of more SiO₂-undersaturatedolivine melilitites from the neighbouring Central Plateau, theexperimental evidence is consistent with either higher concentrationsof H₂O+CO₂ (approaching 14 wt.%), or higher pressures of origin(>35 kb). Petrographic and geochemical evidence suggeststhat the latter is the more probable of the alternatives.     

Partial melting below Tubuai (Austral Islands, French Polynesia)

Process identification diagrams based on trace element data show that mafic lavas from Tubuai, including alkali basalts, basanites, analcitites and nephelinites, result from different degrees of partial melting of an isotopically homogeneous mantle source. Our fractionation-corrected data are consistent with a batch melting model or a dynamic melting model involving a threshold value for melt separation close to 1% and degrees of melting ranging from 5–8% (alkali basalts) to 1.5–3% (nephelinites). The relative source concentration pattern, calculated using an inverse numerical method, shows an enrichment in highly incompatible elements. We propose that the Tubuai lava suite was derived from a two-stage partial melting process. Melting first affected the plume material located within the transition zone between garnet and spinel domains, producing alkali basalts and basanites. Then, the melting zone migrated upwards to the base of the overlying spinel-bearing lithospheric mantle, producing highly silica-undersaturated lavas. The lower lithosphere had previously been enriched by intrusion of pyroxenite veins representing plume-derived melts which percolated away from the main magma conduits. Received: 11 June 1996 / Accepted: 8 January 1997     

The primary geochemistry of the monaro alkaline volcanics,southeastern Australia — evidence for upper mantle heterogeneity

The Mg numbers [100 Mg/(Mg+Fe) atomic ratios] of the Tertiary Monaro alkaline volcanics in southeastern Australia indicate that many of these alkali basalts, basanites and nephelinites have undergone only limited crystal fractionation, and that a few may represent unmodified, unfractionated primary magmas. Fractionation involves essentially olivine and clinopyroxene; fractionation trends are identified by plotting trace-element abundances against Mg number, and are then extrapolated linearly back into the primary magma field to yield estimates of the primary geochemistry of the three rock types.The nephelinites, basanites and alkali basalts are interpreted as a partial melting series derived from a peridotitic upper mantle. The estimated primary abundances of Pb,Th, Ga, V, Cr and Ni are essentially the same for the three rock types, but the estimated primary abundances of K₂O, Rb, Sr, Ba, TiO₂, Zr, Nb, P₂O₅, La Ce, Pr Nd, Y, Cu, and Zn-overlap considerably between the three rock types and the coherence of the incompatible elements as a group is not preserved in the overlaps. These patterns are best accounted for by postulating a patchy distribution of accessory phases such as amphibole, mica and apatite, in the source regions for the Monaro volcanics. Heterogeneities of this kind allow local variation in the volume of partial melt generated at the solidus, and offer a possible solution to magma segregation problems in the upper mantle.     

Cenozoic alkali basaltic magmas of western Germany and their products of differentiation

Analytical data on major elements and 31 trace elements in olivine nephelinites, nepheline basanites, basanitic alkali olivine basalts and their differentiates (tephrites, hawaiites, mugearites, benmoreites, latites, phonolites and trachytes) from Hegau, Kaiserstuhl, Rhön, Hessian Depression, Vogelsberg, Westerwald, Siebengebirge, E Eifel and Hocheifel are evaluated. They were based on 400 samples with new or unpublished data on about one third of the rocks. The Sr–Nd isotopic compositions for 78 rocks are included. The alkali basaltic volcanism is caused by adiabatic decompression of asthenospheric mantle updomed to a minimum depth of 50 km in connection with the Alpine continent collision. The chemical compositions of the primary basaltic melts from the different areas are similar containing about one hundred-fold enrichment of highly incompatible elements relative to the primitive mantle from partial melting of depleted and secondarily enriched peridotite. The elements Cs, K, Pb and Ti are specifically depleted in the basalts partly because of phlogopite being residual at partial melting. The Tertiary alkali basalts range in Nd-isotopic composition from 0.51288 to 0.51273 and in Sr-isotopic ratios from 0.7032 to 0.7042. These ranges indicate mixtures of HIMU, depleted and enriched mantle components in the metasomatically altered peridotite source which resembles that of certain ocean islands. The Nd-Sr-isotopic compositions of the Quaternary E Eifel are close to bulk Earth ratios. East and W Eifel plots differ distinctly from the Tertiary Hocheifel which is geographically intermediate. This isotopic difference, beside specific K/Na ratios, is probably caused by separate metasomatic pulses that immediately preceded the respective periods of volcanism. The metasomatically altered mantle had partly primitive mantle signatures (Nb/Ta, Zr/Sm and Th/U ratios) and partly ocean island (or MORB) source properties (Rb/Cs). A MORB source can be excluded because of the low K/Rb and high Th/U ratios. A correlation of D with ⁸⁷Sr/⁸⁶Sr in amphibole and phlogopite and a slightly larger ¹⁸O than in MORB is conformable with a seawater and crustal impact on the source of alkali basalts. Slightly higher than average water concentrations in the source of certain primary basaltic melts (indicated by amphibole phenocrysts in their basalts) are required for differentiation of these basalts in magma chambers of the upper crust. Model calculations are presented to explain compositions of differentiates which range from about 60% to about 20% residual melt. The latter are represented by phonolites and trachytes. The Nd- and Sr-isotopic signatures of the majority of differentiates indicate contamination by a granitic partial melt from the wall rocks of magma chambers. Olivine nephelinite magma was the common source of contaminated differentiates.     

Deep differentiation of alkali ultramafic magmas: Formation of carbonatite melts

The study of melt microinclusions in olivine megacrysts from meimechites and alkali picrites of the Maimecha–Kotui alkali ultramafic and carbonatite province (Polar Siberia) revealed that the melt compositions corrected for loss of olivine due to post-entrapment crystallization of olivine on inclusion walls (differentiates of primary meimechite magma) match well to the composition of nephelinites and olivine melilitites belonging to carbonatite magmatic series. Modeling of fractional crystallization of meimechite magmas results in the high-alkali melt compositions corresponding to the silicate–carbonate liquid immiscibility field. The appearance of volatile-rich melts at the base of magma-generating plume systems at early stages of partial melting can be explained by extraction of incompatible elements including volatiles, by near-solidus melts at low degrees of partial melting, and meimechites are an example of such magmas. Subsequent accumulation of CO₂ in the residual melt results in generation of carbonate magma.     

Origin of Ross Island basanitoids and limitations upon the heterogeneity of mantle sources for alkali basalts and nephelinites

Primary basanitoids from Ross Island, Antarctica have REE patterns and Pb isotope ratios similar to those for primary alkali basalts and nephelinites on ocean islands. The lead data from all volcanics on Ross Island have a spread of 4% in the 206/204 ratio and give a two-stage model lead age of 1500 m.y. The age is interpreted to be the time since the development of the chemical heterogeneity of the mantle source, presumably during an earlier melting process. Comparison of REE, K, Rb, Sr, Ba and P₂O₅ concentrations for alkali basalts and nephelinites shows that the chondrite normalized mantle source is enriched in light REE with average La/Sm=3.4, Ce/Sm=2.6, Nd/Sm=1.6. Assuming a mantle source with heavy REE abundances of three times chondrites, nephelinites require 3 to 7% partial melting of the mantle source and alkali basalts require 7 to 15% partial melting. The patterns of K, Cu, V and Ti abundances suggest that phlogopite is a residual mineral for most nephelinite, but not alkali basalt mantle sources, and that a sulfide phase and a titanium-rich mineral are in the residual mantle source for both alkali basalts and nephelinites. Small positive Eu anomalies (2–5%) in near primary alkali basalts and nephelinites suggest that the xxx of the mantle sources is 10^?6 to 10^?9 atm. The progressive enrichment of light REE and incompatible elements in the mantle sources for nephelinites and alkali basalts is proposed to result by intrusion of veins of basaltic melt due to very low percentages of melting 1 000 to 3 000 m.y. ago when this part of the deeper mantle was previously involved in convection and partial melting.     

The Petrology of the Tholeiites through Melilite Nephelinites on Gran Canaria, Canary Islands: Crystal Fractionation, Accumulation, and Depths of Melting

We report major and trace element X-ray fluorescence (XRF) datafor mafic volcanics covering the 15-Ma evolution of Gran Canaria,Canary Islands. The Miocene (12–15 Ma) and Pliocene-Quaternary(0–6 Ma) mafic volcanics on Gran Canaria include picrites,tholeiites, alkali basalts, basanites, nephelinites, and melilitenephelinites. Olivineclinopyroxene are the major fractionatingor accumulating phases in the basalts. Plagioclase, Fe–Tioxide, and apatite fractionation or accumulation may play aminor role in the derivation of the most evolved mafic volcanics.The crystallization of clinopyroxene after olivine and the absenceof phenocrystic plagioclase in the Miocene tholeiites and inthe Pliocene and Quaternary alkali basalts and basanites withMgO>6 suggests that fractionation occurred at moderate pressure,probably within the upper mantle. The presence of plagioclasephenocrysts and chemical evidence for plagioclase fractionationin the Miocene basalts with MgO<6 and in the Pliocene tholeiitesis consistent with cooling and fractionation at shallow depth,probably during storage in lower-crustal reservoirs. Magma generationat pressures in excess of 3•0–3•5 GPa is suggestedby (a) the inferred presence of residual garnet and phlogopiteand (b) comparison of FeO¹ cation mole percentages and the CIPWnormative compositions of the mafic volcanics with results fromhigh-pressure melting experiments. The Gran Canaria mafic magmaswere probably formed by decompression melting in an upwellingcolumn of asthenospheric material, which encountered a mechanicalboundary layer at {small tilde}100-km depth.     

Petrogenesis of Tertiary Mafic Alkaline Magmas in the Hocheifel, Germany

Primitive nephelinites and basanites from the Tertiary Hocheifelarea of Germany (part of the Central European Volcanic Province;CEVP) have high Mg-number (>0·64), high Cr and Nicontents and strong light rare earth element enrichment butsystematic depletion in Rb, K and Ba relative to trace elementsof similar compatibility in anhydrous mantle. Alkali basaltsand more differentiated magmatic rocks have lower Mg-numberand lower abundances of Ni and Cr, and have undergone fractionationof mainly olivine, clinopyroxene, Fe–Ti oxide, amphiboleand plagioclase. Some nephelinites and basanites approach theSr–Nd–Pb isotope compositions inferred for the EAR(European Asthenospheric Reservoir) component. The Nd–Sr–Pbisotope composition of the differentiated rocks indicates thatassimilation of lower crustal material has modified the compositionof the primary mantle-derived magmas. Rare earth element meltingmodels can explain the petrogenesis of the most primitive maficmagmatic rocks in terms of mixing of melt fractions from anamphibole-bearing garnet peridotite source with melt fractionsfrom an amphibole-bearing spinel peridotite source, both sourcescontaining residual amphibole. It is inferred that amphibolewas precipitated in the asthenospheric mantle beneath the Hocheifel,close to the garnet peridotite–spinel peridotite boundary,by metasomatic fluids or melts from a rising mantle diapir orplume. Melt generation with amphibole present suggests relativelylow mantle potential temperatures (<1200°C); thus themantle plume is not thermally anomalous. A comparison of recentlypublished Ar/Ar ages for Hocheifel basanites with the geochemicaland isotopic composition of samples from this study collectedat the same sample sites indicates that eruption of earlierlavas with an EM signature was followed by the eruption of laterlavas derived from a source with EAR or HIMU characteristics,suggesting a contribution from the advancing plume. Thus, theHocheifel area represents an analogue for magmatism during continentalrift initiation, during which interaction of a mantle plumewith the overlying lithosphere may have led to the generationof partial melts from both the lower lithosphere and the asthenosphere. KEY WORDS: alkali basalts; continental volcanism; crustal contamination; partial melting; Eifel, Germany     

Origin of the Tertiary basaltic volcanism in the northern Hessian Depression

Volcanic activity started about 20 Ma before present with quartz tholeiites (QTh), had a climax with alkali olivine basalts (AOB) 13 to 14 Ma ago and ended 7 Ma ago with nepheline basanites (NB) and olivine nephelinites (ON). AOB covers 73% of the volcanic area. About 250 basalts and peridotite xenoliths were sampled for investigation. An upper mantle layer ranging from about 90 to 60 km depth has been conditioned for a preferential alkali basalt production by advection of H₂O-CO₂-fluids containing Si, Al, Ca, K, Na, P as major constituents beside numerous incompatible minor elements. At the onset of the geodynamically triggered mantle conditioning locally restricted diapirism into shallow depth has caused formation of olivine tholeiite magmas (OTh) at about 1,300° C by partial melting. All of these OTh primary melts intruded due to a favourable compressibility into granulites of the lower crust. The rare QTh basalts are their derivative magmas which have been slightly contaminated in the crust. Magmas of the subsequent alkali basaltic volcanism (AOB, bAOB, NB, ON, MON) formed by in-situ partial melting at about 75 to 90 km depth after depression of the peridotite solidi by fluids to temperatures 1,200° C. Except many AOB these magmas are primary melts as characterized by olivine/melt distribution coefficients of Mg/Fe²⁺ (K _D=0.29 to 0.34), by Ni concentrations (260 to 330 ppm) and the occurrence of peridotite xenoliths. Rapid rise of gas charged melts due to saturation in CO₂ prevented separation of olivine etc. and of xenoliths. The sequence of magmas from OTh to ON (or MON) is formed from decreasing proportions of orthopyroxene (opx) and increasing contributions of clinopyroxene (cpx) and phlogopite (ph) at almost equal proportions of spinel (sp). Incongruent melting of opx (and cpx) for OTh, AOB, NB and ON is correlated with precipitation of olivine. The average xenolith composition (73% ol, 18% opx, 7% cpx, 1.1% sp and 1.3/0.5% ph) was used to model the sources of the investigated melts by 9 incompatible elements and to calculate degrees of partial melting. The occurrence of garnet cannot be reliably excluded by modelling on the basis of HREE distribution coefficients. The average xenolith composition was used for modelling because of its resemblance with worldwide sampled depleted mantle inclusions. For avoiding to exhaust at least one mineral of the model mantle in the support of the norm composition of OTh, AOB, NB and MON magmas the degrees of partial melting cannot exceed 12.5%, 6%, 6% and 4% respectively. Mantle containing about 500 ppm K (and the correlated incompatible elements), like the average of 36 xenoliths, allows to explain the formation of OTh magmas. AOB, NB and ON melts require peridotite with slightly less than 1,500 ppm K, 670 ppm P and proportions of the correlated elements LREE, Sr, Ba, Zr, Rb, Cs, Ta, Th, Hf, U, which are higher than their abundance in primitive mantle rocks. About 20% of the xenoliths have this composition. Metasomatism of fluids with these elements must have been an immediate precursor of the alkali basaltic volcanism. Otherwise the preservation of a local disequilibrium in ⁸⁷Sr/⁸⁶Sr ratios between cpx cores and total rock at upper mantle temperatures cannot be explained.     

The composition and formation of Miocene tholeiites in the Central European Cenozoic plume volcanism (CECV)

Tholeiites accompanying a majority of alkali basalts are restricted to the highly productive central part of the CECV plume activity in Vogelsberg and Hessian Depression. They mainly occur as quartz tholeiites which according to experiments of partial melting and material balances are products of olivine tholeiitic primary melts. The differentiation from olivine to quartz tholeiitic melts took place in lower crustal magma chambers where olivine tholeiitic melt intruded due to a density comparable with that of the country rocks. The fractionation due to separation of olivine and some clinopyroxene caused contamination of tholeiite magmas by tonalitic partial melts from the wall rocks of the magma chambers. The latter process is indicated by relatively high Rb, K and Pb and low Nb concentrations and by Nd, Sr and Pb isotopes. Contaminating crustal melts, which roughly attained a proportion of 10%, contained very low ¹⁴³Nd/¹⁴⁴Nd ratios from a Nd/Sm fractionation as old as 2.6 Ga. This is the first evidence from mafic rocks of this high age in the lower crust beneath Central Europe. Modelling with incompatible elements allows to recognize olivine tholeiites as products of about 1% partial melting of plume rocks consisting of 35% primitive and 65% depleted mantle materials. The production of tholeiites other than alkali basalts is restricted to the highest plume activity and the largest fraction of MORB type source rocks. Received: 10 December 1999 / Accepted: 23 June 2000     

Alkaline volcanism in the history of the Norwegian-Greenland basin

The opening of the North Atlantic Ocean began in the Late Paleocene and was accompanied by the eruption of submarine and subaerial basalts, which built up submarine plateau and ridges, islands, and volcanoes. The volcanic rocks are dominated by low-K tholeiitic basalts, which associate with almost coeval alkaline rocks (subalkali and alkali basalts and their derivatives, basanites, nephelinites, and others). The oldest alkaline volcanics (58–56 Ma) were formed during the opening of the oceanic rift at its shoulders, in northeastern Greenland and the western Norwegian shelf. It was recently found that 55–53 Ma-old alkali-ultramafic rocks are much more widespread at the eastern coast of Greenland than it was previously thought. The younger occurrences of alkali volcanism with pulses at 30, 10, 5 Ma, and up to the present day were formed on the young oceanic plate and newly formed islands and seamounts. To compare the oceanic and continental volcanism of this region, oceanic volcanics dredged during Cruise 10 of the R/V Akademik Kurchatov were reanalyzed using modern analytical methods (XRF and ICP-MS). This study showed that the oceanic and continental alkaline rocks are significantly different in petrochemical and geochemical characteristics, which is caused by differences in magma generation depths and compositions of the mantle source material. The primary continental alkaline magmas were initially more enriched in incompatible trace elements than oceanic ones. During the shallow-level differentiation of oceanic magmas, trace elements and alkalis could be accumulated in residual melts, but these processes occurred on a minor scale and depended on tectonic conditions.     

Volcanism of the Kerguelen Plateau (Indian Ocean): Composition,Evolution, and Sources

Petrographic and geochemical study of basalts in the Kerguelen Plateau basement revealed changes in the composition and character of volcanism during the development of this tectonovolcanic structure. The Kerguelen Plateau is one of the largest intraplate rises in the World Ocean. It started to form about 120 Ma ago. The age of basalts and overlying sediments shows that the plateau formation succeeded in the northwestern direction. Basalts of the Kerguelen Plateau basement are products of tholeiitic melts in terms of geochemistry, but differ from the mid-oceanic ridge basalt (MORB). They are enriched in incompatible trace elements and rare earth elements (REE) relative to MORB, and the degree of enrichment varies in basalts from different segments of the plateau. The composition of basalts does not directly depend on their age. Specific features of the plateau magmatism are commonly explained in terms of a long-living deep magma plume, which variously interacted with a depleted upper mantle source at different stages of the plateau formation. However, taking into account block morphology and deep structure of the plateau, one can suggest that the plateau volcanism was initiated by a large fault. As the volcanism prograded to the northwest, the depth of fault penetration into the mantle changed. The composition of basalts in the plateau basement was also governed by the formation depth of primary melts.     

Petrologic variations in quaternary volcanic rocks,British Columbia,and the nature of the underlying upper mantle

Volcanic activity has produced Late Tertiary and Quaternary cinder cones and flows between the Snake River Plain, U.S.A. and the Yukon Territory, Canada. The rock types include basanites, alkali olivine basalts, high-iron basalts, hawaiites, ankaramites, nephelinites, and olivine tholeiites. The alkali olivine basalts, basanites and hawaiites sampled are chemically similar to rocks from the mid-Atlantic islands. Associated with the volcanic rocks are xenoliths of ultramafic rocks, gabbros, granites and granulites.Seismic data indicate that the Moho throughout the region dips eastward at a very shallow angle. The low velocity zone has been located beneath southern British Columbia and displays a topographic high trending northwest-southeast. The nephelinite was erupted from near the crest of this high with less undersaturated lavas erupted from along its flanks.The suite of ultramafic xenoliths spans a greater variety of rock types than can be generated by maximum amounts of partial melting of a uniform source material to produce the lavas in the region. Calculated residual olivine compositions in equilibrium with the magmas at low velocity zone depths and liquidii temperatures are more iron-rich than the typical lherzolite xenolith olivine. This suggests that the residua from the partial melting episodes which produced the volcanic rocks are different from the upper mantle lid above the low velocity zone as represented by the ultramafic xenoliths.     

Petrogenesis of the Largest Intraplate Volcanic Field on the Arabian Plate (Jordan): a Mixed Lithosphere-Asthenosphere Source Activated by Lithospheric Extension

Miocene to Recent volcanism in northwestern Arabia producedthe largest intraplate volcanic field on the Arabian plate (HarratAsh Shaam, Jordan). The chemically and isotopically diversevolcanic field comprises mafic alkali basalts and basanites.The magmas underwent limited fractional crystallization of ol± cpx ± plag and rare samples have assimilatedup to 20% of Late Proterozoic crust en route to the surface.However, there are subtle Sr–Nd–Pb isotopic variations(⁸⁷Sr/⁸⁶Sr = 0·70305–0·70377, ¹⁴³Nd/¹⁴⁴Nd= 0·51297–0·51285, ²⁰⁶Pb/²⁰⁴Pb = 18·8–19·2),which exhibit marked correlations with major elements, incompatibletrace element ratios and abundances in relatively primitivebasalts (MgO >8·5 wt %), and cannot be explained byfractional crystallization and crustal contamination alone.Instead, the data require polybaric melting of heterogeneoussources. Semi-quantitative melt modelling suggests that thisheterogeneity is the result of small degree melts (2–5%)from spinel- and garnet-facies mantle, inferred to be shallowArabian lithosphere, that mixed with smaller degree melts (<1%)from a predominantly deep garnet-bearing asthenospheric(?) sourcewith ocean island basalt characteristics. The latter may bea ubiquitous part of the asthenosphere but is preferentiallytapped at small degrees of partial melting. Volcanism in Jordanappears to be the result of melting lithospheric mantle in responseto lithospheric extension. With time, thinning of the lithosphereallowed progressively deeper mantle (asthenosphere?) to be activatedand melts from this to mix with the shallower lithospheric mantlemelts. Although Jordanian intraplate volcanism is isotopicallysimilar to examples of Late Cenozoic volcanism throughout theArabian peninsula (Israel, Saudi Arabia), subtle chemical andisotopic differences between Yemen and Jordan intraplate volcanismsuggest that the Afar plume has not been channelled northwestwardsbeneath the Arabian plate and played no role in producing thenorthern Saudi Arabian and Jordan intraplate volcanic fields. KEY WORDS: asthenosphere; intraplate volcanism; Jordan; lithospheric mantle; Sr–Nd–Pb isotopes     

Nature and Evolution of Cenozoic Lithospheric Mantle beneath Shandong Peninsula,Sino-Korean Craton,Eastern China

The Shanwang and Qixia basalts lie within the North China block and were erupted in Miocene to Pliocene time (18.1 to 4.3 Ma) and Pliocene time (6.4 to 5.9 Ma), respectively. The Shanwang area lies astride the Tancheng-Lujiang (Tanlu) fault zone, a major lithospheric fault, whereas the Qixia area lies east of the fault zone. The basaltic rocks (alkali olivine basalts, basanites, nephelinites) carry abundant deep-seated xenoliths including spinel lherzolite (dominant), dunite, and pyroxenite, and a megacryst suite including augite, anorthoclase, phlogopite, ilmenite, and garnet. Xenoliths with coarse-grained microstructures are common in the Qixia xenolith suite, but are absent in Shanwang. Reconstructed bulk compositions of the lherzolites range from relatively depleted (<3% modal diopside) to fertile (>12% modal diopside). Equilibration temperatures of 850° to 1020°C indicate entrainment of these lherzolites from depths ≤45 km, within the lithosphere; the geotherm may have been higher beneath Shanwang. The Shanwang suite contains less-depleted lherzolites, and more pyroxenites, than the Qixia suite. The chondrite-normalized REE patterns in clinopyroxenes of the Shandong xenoliths vary from LREE depleted, through concave shaped, to LREE enriched; spidergrams for the clinopyroxenes can be divided into depleted, fertile, and metasomatic types. Progressive depletion in Na and Al is accompanied by depletion in moderately incompatible elements such as Y, Yb, and Zr, and an increase in Mg#. Ti and Zr in clinopyroxenes have not been affected by the metasomatic process, and MREE have been little disturbed, whereas the light rare-earth elements, Nb, and Sr have been strongly enriched during metasomatism; this suggests that carbonate-rich fluids/melts were the metasomatic agent. The mantle beneath the Shandong Peninsula sampled by these basalts is dominantly Phanerozoic in character rather than Archean or Proterozoic lithospheric mantle. This mantle probably represents a mixture of older lithospheric mantle and newly accreted material that replaced the Archean lithospheric keel through extension, thermal erosion, and fluid/melt metasomatism. The differences in micro-structures, chemistry, temperature, and fluid/melt activity between Shanwang and Qixia are ascribed to their spatial relationships to the Tanlu fault, which is a major translithospheric suture that hasplayed an important role in the Cenozoic replacement of the pre-existing Archean lithospheric mantle.     

The systematics of lithium abundances in young volcanic rocks

Lithium is a moderately incompatible trace element in magmatic systems. High precision analyses for lithium conducted on well characterized suites of MORB and ocean island basalts suggest a bulk distribution coefficient of 0.25−0.35 and behavior which is similar to Yb during low pressure fractionation and V during melting, as long as garnet is not an important residual phase. Data for peridotites and basalts suggest a mantle lithium content of about 1.9 ppm and show that significant concentrations of lithium reside in olivine and orthopyroxene, resulting in unusual inter-mineral partitioning of Li and complex relationships between lithium and other incompatible trace elements.The lithium abundances of arc basalts are similar to those of MORB, but their Li/Yb ratios are considerably higher. The high Li/Yb suggests the addition of a Li-rich component to arc sources; relatively low Yb abundances are consistent with the derivation of some arc magmas by larger extents of melting or from a more depleted source than MORB. Although Li is enriched at arcs, K is enriched more, leading to elevated K/Li ratios in arc volcanics. The high K/Li and relatively low La/Yb of primitive arc basalts requires either incorporation of altered ocean crust into arc magma sources, or selective removal of K and Li from subducted sediments. Bulk incorporation of sediments alone does not explain the Li systematics.Data from primitive MORB indicate a relatively low (3–4 ppm) Li content for new oceanic crust. Thus, the Li flux from the ocean crust is probably <1 × 10¹¹ g/yr, and the oceanic crust may not be an important net source in the oceanic budget of lithium.     

Origin of Late Cenozoic Abaga–Dalinuoer basalts,eastern China: Implications for a mixed pyroxenite–peridotite source related with deep subduction of the Pacific slab

Continental intraplate basalts (15.42–0.16 Ma) from Abaga–Dalinuoer volcanic field (ADVF) in central Inner Mongolia of eastern China, as a part of Cenozoic volcanic province along eastern margin of the Eurasian continent, provide a good opportunity to explore potential links between deep subduction of the Pacific slab and continental intraplate volcanism. In this study, we report an integrated dataset of whole-rock K–Ar ages, major and trace elements and Sr–Nd–Pb isotopes, and olivine major and minor elements for the Abaga–Dalinuoer basalts (ADBs), and propose that mantle source lithology of the ADB magmas may consist of both pyroxenite and peridotite. The ADBs display low SiO₂ (42.3–50.2 wt.%), high MgO (7.3–11.4 wt.%) and moderate K₂O + Na₂O (3.8–6.4 wt.%), and can be subdivided into basanites, alkali basalts and tholeiitic basalts that are all characterized by ocean island basalt (OIB)-like rare earth elements (REE) and enrichment in both large ion lithosphile elements (LILE) and high field strength elements (HFSE). Olivine phenocrysts have higher Ni and Fe/Mn and lower Mn, Ca and Ca/Fe relative to those from peridotite melts, but exhibit clearly lower Ni contents (< 2500 ppm) compared with expected Ni range (> 3000 ppm) for olivines crystallized from olivine-free pyroxenite melts. Estimated compositions of the ADB primary magmas, together with olivine compositions, suggest an iron-rich mantle source related with silica-deficient pyroxenite that is most likely derived from deeply subducted Pacific oceanic crust. Additionally, peridotite and recent subducted sediments are also required to account for high Ni and MgO in primary magmas together with their trace elements and Sr–Nd–Pb isotope systematics. We suggest that a mixed pyroxenite–peridotite source lithology can better match observed whole-rock and olivine signatures in the ADB, compared with either peridotite only or olivine-free pyroxenite only source lithology. In our model, pyroxenite melts would either react with or mechanically mix with peridotite, and the proportion of pyroxenite melts may range from 30% to 45% for mechanical mixing scenario. A continuous spectrum from tholeiitic to alkali melts revealed by melt-peridotite reaction experiment can explain formation of primary magmas of basanites, alkali basalts and tholeiitic basalts by increasing melting degree of a similar mantle source. Relatively higher ²⁰⁶Pb/²⁰⁴Pb of the ADB may suggest more significant role of recent (< 0.5 Ga) subducted Pacific oceanic materials, in contrast to other Cenozoic basalts in eastern China (e.g., Changbai basalts) that exhibit varying contributions from ancient (> 1.5 Ga) subducted continental sediments. We emphasize that coupled geochemical and geodynamic links (i.e., subduction polarity) between deeply subducted Pacific slab and continental intraplate volcanism in eastern China may exist, which directly support the involvement of deeply subducted Pacific materials in petrogenesis of the ADB. From the perspective of plate motion kinetics, decompression partial melting of upwelling fragmented Pacific slab (silica-deficient pyroxenite + recent subducted sediments) may be triggered by rollback of deeply subducted Pacific slab during Late Cenozoic times. Continental intraplate volcanism in the ADVF generally started with termination of opening of the Japan Sea, suggesting that deep subduction of the Pacific slab may have been an important geodynamic mechanism responsible for tectono-magmatic evolution of northeastern Asia. We suggest that the ADBs have the potential to shed light on genetic links between continental intraplate volcanism and deep subduction of the Pacific slab in geochemical and geodynamic processes.     

Evidence for heterogenes primary MORB and mantle sources,NW Indian Ocean

Basalts from 5 Deep Sea Drilling Project (DSDP) sites in the northwest Indian Ocean (Somali Basin and Arabian Sea) have general geochemical features consistent with a spreading origin at the ancient Carlsberg Ridge. However, compared to most MORBS from other oceans they have low normative olivine, TiO₂, and Zr contents. There is no evidence that the mantle source of these northwest Indian Ocean basalts was enriched in incompatible elements relative to the Atlantic and Pacific ocean mantles. In detail, incompatible element abundances in these DSDP basalts establish that they evolved from several compositionally distinct parental magmas. In particular, basalts from site 236 in the Somali Basin have relatively high SiO₂ and low Na, P, Ti, and Zr contents. These compositional features along with low normative olivine contents are similar to those proposed for melts derived by two-stage (or dynamic) melting. Published data also indicate there is no enrichment in incompatible elements at the southwest Indian Ocean triple junction, although southwest Indian Ocean basalts have slightly higher ⁸⁷Sr/⁸⁶Sr than normal Atlantic MORB. The data suggest that there are significant subtle geochemical variations in the Indian Ocean mantle sources, but are insufficient to show whether these variations have a systematic temporal or geographic distribution.     

Rare earth contribution to the origin of Hawaiian lavas

Rare earth abundances were determined by neutron activation in twenty Hawaiian lavas and one diabase of known chemical and mineralogical compositions. These results demonstrate a systematic relationship between the absolute or relative rare earth abundances and the petrochemistry of these rocks. Three distinct lava groups are recognized. These correspond to: (1) tholeiites, (2) alkali series, (3) nepheline-melilite basalts.Based on rare earths: a) The hawaiites and mugearite of the alkali series represent residual melts derived from alkali olivine basalts, most likely by fractional crystallization; the trachyte, however, seems to have a more complicated history. b) Fractional crystallization models linking nephelinites or alkali olivine basalts to tholeiites are possible. However, production of these three lava groups, independently, by various degrees of partial melting of the mantle is equally likely and cannot be distinguished from these fractional crystallization models. c) Daly limestone syntexis hypothesis to produce the nephelinites is unlikely.     

Middle/Late Cambrian intracontinental rifting in the central West Sudetes,NE Bohemian Massif (Czech Republic): geochemistry and petrogenesis of the bimodal metavolcanic rocks

The Early Palaeozoic East Krkonoše Complex (EKC) situated in the central West Sudetes, NE Bohemian Massif, is a volcano‐sedimentary suite containing abundant mafic and felsic volcanics metamorphosed to greenschist facies. The trace element distribution patterns and Nd isotope signatures (E_Nd500 = + 3.1 to + 6.6) of the metabasites (metabasalts) indicate that they may be related to a rising mantle diapir associated with intracontinental rifting. At the early stage, limited melting of an upwelling asthenosphere produced alkali basalts and enriched tholeiites which compositionally resemble oceanic island basalts. A later stage of rifting with larger degrees of melting at shallower depths generated tholeiitic basalts with E‐MORB to N‐MORB characteristics. The values of (⁸⁷Sr/⁸⁶Sr)_i = 0.706 and E_Nd500 = − 5 ±1 of the porphyroids (metarhyolites) as well as the lack of rocks with intermediate compositions suggest that the felsic rocks were formed by a partial melting event of continental crust triggered by mantle melts. The geochemistry of the EKC bimodal metavolcanics and their association with abundant terrigenous metasediments suggest that the felsic–mafic volcanic suite was generated during intracontinental rifting. This process, widespread in Western and Central Europe during the Early Palaeozoic, is evidence of large‐scale fragmentation of the northern margin of the Gondwana supercontinent. Copyright © 2001 John Wiley & Sons, Ltd.