Geochemistry and geochronology of the mafic lavas from the southeastern Ethiopian rift (the East African Rift System): assessment of models on magma sources,plume–lithosphere interaction and plume evolution

Major and trace element and isotopic ratios (Sr, Nd and Pb) are presented for mafic lavas (MgO > 4 wt%) from the southwestern Yabello region (southern Ethiopia) in the vicinity of the East African Rift System (EARS). New K/Ar dating results confirm three magmatic periods of activity in the region: (1) Miocene (12.3–10.5 Ma) alkali basalts and hawaiites, (2) Pliocene (4.7–3.6 Ma) tholeiitic basalts, and (3) Recent (1.9–0.3 Ma) basanite-dominant alkaline lavas. Trace element and isotopic characteristics of the Miocene and Quaternary lavas bear a close similarity to ocean island basalts that derived from HIMU-type sublithospheric source. The Pliocene basalts have higher Ba/Nb, La/Nb, Zr/Nb and ⁸⁷Sr/⁸⁶Sr (0.70395–0.70417) and less radiogenic Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb = 18.12–18.27) relative to the Miocene and Quaternary lavas, indicative of significant contribution from enriched subcontinental lithospheric mantle in their sources. Intermittent upwelling of hot mantle plume in at least two cycles can explain the magmatic evolution in the southern Ethiopian region. Although plumes have been originated from a common and deeper superplume extending from the core–mantle boundary, the diversity of plume components during the Miocene and Quaternary reflects heterogeneity of secondary plumes at shallower levels connected to the African superplume, which have evolved to more homogeneous source.     

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     

Petrogenesis and evolution of Mt. Vulture alkaline volcanism (Southern Italy)

Summary The Late Pleistocene Mt. Vulture strato-volcano developed at the intersection of NE-SW and NW-SE lithospheric fault systems, on the easternmost border of the Apennine compressional front overthrust onto the Apulian foreland. The initial phase of the volcanic activity is represented by pyroclastic deposits, including lava blocks, and subordinate eccentric domes, mostly phonolitic in composition. The later stages of activity formed the bulk of the strato-volcano (pyroclastic products and subordinate lavas), mostly tephritic in composition, with minor intercalations of basanite, mela-foidite and melilitite lavas and dikes. Variations in rock and mineral composition suggest that the volumetrically predominant basanite-tephrite (foidite)-phonotephrite-phonolite series can be accounted for by fractional crystallization processes starting from basanitic parental magmas, in agreement with the remarkably constant ⁸⁷Sr/⁸⁶Sr isotopes (0.70586–0.70581). Mass-balance calculations indicate that the variably differentiated magmas may have been produced by removal of wehrlite, clinopyroxenite and syenite cumulates, some of which are occasionally found as cognate xenoliths in the volcanics. Fractionation processes probably developed in multiple-zoned magma chambers, at depths of 3–5 km, corresponding to the tectonic discontinuity between the allochthonous Apennine formations and the underlying Apulian platform. Highly differentiated phonolitic magmas capping the magma chambers and their conduits thus appear to have fed the initial volcanic activity, whereas dominantly tephritic products were erupted in later stages. The least evolved mafic magmas, namely basanites, mela-foidites and melilitites, are characterized by diverse Na/K ratios and critical SiO₂-undersaturation, which indicate their derivation as independent melts generated from distinct, heterogeneously enriched mantle sources and by variable partial melting degrees. Primitive mantle-normalized incompatible element patterns of Vulture mafic lavas invariably share analogies with both orogenic subduction-related magmas (high Low Field Strength Elements/High Field Strength Elements ratios, K, Rb and Th contents and marked Ti and Nb negative anomalies) and alkaline lavas from within-plate and rift settings (high Light Rare Earth Elements, P, Zr, Nb and Na). These geochemical features may be accounted for by magma generation from deep lithospheric mantle sources, enriched in Na-alkali silicate/carbonatite anorogenic components, subsequently affected by orogenic subduction-related K-metasomatism, analogous to that which modified magma sources of the Roman Magmatic Province along the internal Apennine Chain. Received April 12, 2000; revised version accepted June 7, 2001     

The Role of Partial Melting in the 15-Ma Geochemical Evolution of Gran Canaria: A Blob Model for the Canary Hotspot

The subaerial portion of Gran Canaria, Canary Islands, was builtby three cycles of volcanism: a Miocene Cycle (8•5–15Ma), a Pliocene Cycle (1•8–6•0 Ma), and a QuaternaryCycle (1•8–0 Ma). Only the Pliocene Cycle is completelyexposed on Gran Canaria; the early stages of the Miocene Cycleare submarine and the Quaternary Cycle is still in its initialstages. During the Miocene, SiO₂ saturation of the mafic volcanicsdecreased systematically from tholeiite to nephelinite. Forthe Pliocene Cycle, SiO₂ saturation increased and then decreasedwith decreasing age from nephelinite to tholeiite to nephelinite.SiO₂ saturation increased from nephelinite to basanite and alkalibasalt during the Quaternary. In each of these cycles, increasingmelt production rates, SiO₂ saturation, and concentrations ofcompatible elements, and decreasing concentrations of some incompatibleelements are consistent with increasing degrees of partial meltingin the sequence melilite nephelinite to tholeiite. The maficvolcanics from all three cycles were derived from CO₂-rich garnetlherzolite sources. Phlogopite, ilmenite, sulfide, and a phasewith high partition coefficients for the light rare earth elements(LREE), U, Th, Pb, Nb, and Zr, possibly zircon, were residualduring melting to form the Miocene nephelinites through tholeiites;phlogopite, ilmenite, and sulfide were residual in the sourceof the Pliocene–Quaternary nephelinites through alkalibasalts. Highly incompatible element ratios (e.g., Nb/U, Pb/Ce,K/U, Nb/Pb, Ba/Rb, Zr/Hf, La/Nb, Ba/Th, Rb/Nb, K/Nb, Zr/Nb,Th/Nb, Th/La, and Ba/La) exhibit extreme variations (in manycases larger than those reported for all other ocean islandbasalts), but these ratios correlate well with degree of melting.Survival of residual phases at higher degrees of melting duringthe Miocene Cycle and differences between major and trace elementconcentrations and melt production rates between the Mioceneand Pliocene tholeiites suggest that the Miocene source wasmore fertile than the Pliocene–Quaternary source(s). We propose a blob model to explain the multi-cycle evolutionof Canary volcanoes and the temporal variations in chemistryand melt production within cycles. Each cycle of volcanism representsdecompression melting of a discrete blob of plume material.Small-degree nephelinitic and basanitic melts are derived fromthe cooler margins of the blobs, whereas the larger-degree tholeiiticand alkali basaltic melts are derived from the hotter centersof the blobs. The symmetrical sequence of mafic volcanism fora cycle, from highly undersaturated to saturated to highly undersaturatedcompositions, reflects melting of the blob during its ascentbeneath an island in the sequence upper margin-corelower margin.Volcanic hiatuses between cycles and within cycles representperiods when residual blob or cooler entrained shallow mantlematerial fill the melting zone beneath an island.     

The Ethiopian subcontinental mantle domains: geochemical evidence from Cenozoic mafic lavas

Summary Since the Cenozoic, Ethiopia was affected by a widespread volcanic activity related to the geodynamic evolution of the Afar triple junction. The plateau building phase was followed by the formation of the Main Ethiopian Rift (MER) accompanied by a bimodal volcanic activity in both the inner parts of the rift and its shoulders. Outside the rift, a concurrent volcanic activity occurred mainly along transversal tectonic lineaments, the most important of which is the Yerer-Tullu Wellel Volcano-Tectonic Lineament (YTVL) developing for ∼500 km westward of Addis Abeba. Scattered Pliocene – Quaternary volcanoes are reported also inside the plateau such as those out cropping nearby Lake Tana. Here we present the result of a study on carefully screened mafic lavas outcropping in two sectors located off-axis the MER, namely, the YTVL and the southern part of Lake Tana; and in one sector located in the southern tip of the MER close to Megado, in the Sidamo region. The screened samples are petrographically fresh and have SiO₂<52 wt.% and MgO>4 wt.%, to minimise crystal fractionation effects. Most of the samples belong to the Late Miocene – Quaternary volcanic activity of the East African Rift System (EARS), although a number of samples along the YTVL are representative of the Late Eocene – Early Miocene Ethiopian Volcanic Plateau flood basalts. The selected mafic lavas offer the opportunity to assess the geochemical diversity, if any, of the subcontinental mantle domains along the MER (Megado and the easternmost part of the YTVL) and in sectors far away from the MER (YTVL and Lake Tana). The samples have a wide compositional range: from basanite to alkali basalt, hy-normative basalt, qz-normative basalt, basaltic andesite, hawaiite, trachybasalt, and trachyandesite. The major and trace element characteristics of the mafic lavas demonstrate an origin from a relatively fertile and trace element enriched lithospheric mantle at pressure variable from ∼2.0 to 3.5 GPa. Moreover, systematic variations in K/Nb, Ba/Nb, and Ba/Rb demand for the contribution of trace amounts of phlogopite to melt production. The geochemical signature coupled with the geographical distribution of the Late Miocene – Quaternary samples along the YTVL (∼500 km) and the Lake Tana and Megado sectors set constraints on a relatively homogenous lateral continuity of the deeper lithospheric mantle domains (∼2–3.5 GPa). On the other hand, the trace element characteristics of the Ethiopian Volcanic Plateau samples along the YTVL, demand for a chromatographic process en route to the surface and indicate a shallower lithospheric mantle domain (<2 GPa) with a different geochemical signature. Overall, the selected mafic lavas provide evidence for vertically zoned lithospheric mantle domains: the shallower domain (<2 GPa) consists of an enriched mantle component with a geochemical signature similar to continental crust material (EM II), whilst the deeper domain (∼2–3.5 GPa) consists of an enriched component similar to the average composition of the subcontinental lithospheric mantle (SCLM). Supplementary material to this paper is available in electronic form at Appendix available as electronic supplementary material     

Erosion of lithospheric mantle beneath the East African Rift system: geochemical evidence from the Kivu volcanic province

This study presents new major and trace element and Sr–Nd isotopic results for a suite of Miocene–Recent mafic lavas from the Kivu volcanic province in the western branch of the East African Rift. These lavas exhibit a very wide range in chemical and isotopic characteristics, due to a lithospheric mantle source region that is heterogeneous on a small scale, probably <1 km. The chemical and isotopic variations are mostly geographically controlled: lavas from Tshibinda volcano, which lies on a rift border fault on the northwestern margin of the province, have higher values of ⁸⁷Sr/⁸⁶Sr, (La/Sm)_n, Ba/Nb, and Zr/Hf than the majority of Kivu (Bukavu) samples. The range of ⁸⁷Sr/⁸⁶Sr at Tshibinda (0.70511–0.70514) overlaps some compositions found in the neighboring Virunga province, while Bukavu group lavas include the lowest ⁸⁷Sr/⁸⁶Sr (0.70314) and highest _Nd (+7.6) yet measured in western rift lavas. The Tshibinda compositions trend towards a convergence for Sr–Nd–Pb isotopic values among western rift lavas. Among Kivu lavas, variations in ¹⁴³Nd/¹⁴⁴Nd correlate with those for certain incompatible trace element ratios (e.g., Th/Nb, Zr/Hf, La/Nb, Ba/Rb), with Tshibinda samples defining one compositional extreme. There are covariations of isotopic and trace element ratios in mafic lavas of the East African Rift system that vary systematically with geographic location. The lavas represent a magmatic sampling of variations in the underlying continental lithospheric mantle, and it appears that a common lithospheric mantle (CLM) source is present beneath much of the East African Rift system. This source contains minor amphibole and phlogopite, probably due to widespread metasomatic events between 500 and 1000 Ma. Lava suites which do not show a strong component of the CLM source, and for which the chemical constraints also suggest the shallowest magma formation depths, are the Bukavu group lavas from Kivu and basanites from Huri Hills, Kenya. The inferred extent of lithospheric erosion therefore appears to be significant only beneath these two areas, which is generally consistent with lithospheric thickness variations estimated from gravity and seismic studies.     

Petrology and geochemistry of Pan-African granitoids, Kab Amiri area, Egypt – implications for tectonomagmatic stages in the Nubian Shield evolution

Summary Three distinctive metaluminous granitic suites have been identified from the Pan-African belt of the Kab Amiri area, Eastern Desert, Egypt. These are: 1) a trondhjemite-tonalite suite, 2) a calc-alkaline granodiorite suite, and 3) an alkali leucogranite suite. The trondhjemite-tonalite and the granodiorite suites resemble I-type granitoids whereas the alkali leucogranites display A-type characteristics. Geochemical attributes and field aspects indicate that three independent magmas, at different tectonic stages of the Pan-African crustal growth, are required to explain the origin of these granitoid suites. Rocks of the trondhjemite-tonalite suite correspond to granites of the arc stage and possess a narrow range of SiO₂ with low K₂O, Sr, Rb, Ba, Nb and Zr. Its composition is consistent with 20–30% partial melting of a primitive low-K tholeiitic source, similar to the early formed tholeiitic metavolcanics of the Egyptian basement. The granodiorite suite belongs to the collision stage and displays higher K₂O, Rb, Ba, and Sr. Its magma was derived by 30–40% partial melting of LILE-enriched mafic island arc crust. The presence of abundant microdiorite enclaves in the trondhjemite-tonalite and the granodiorite suites suggests that mantle-derived mafic magma played an important role in their petrogenesis, acting as a heat source for melting via underplating and/or intrusion. The A-type leucogranites are post-collision highly fractionated granites. They exhibit low Al₂O₃, MgO, CaO, TiO₂, Sr, and Ba and high Rb, Nb, Y. The wide chemical variations within this suite are consistent with its evolution by fractional crystallization of plagioclase, K-feldspar, amphibole, Fe–Ti oxides, and apatite from a mafic magma. The parent magma was originated in the upper mantle due to crustal attenuation associated with extension in the late stage of the Pan-African crustal evolution. Received September 13, 2000; revised version accepted May 4, 2001     

Melting in the lithospheric mantle: Inverse modelling of alkali-olivine basalts from the Big Pine Volcanic Field,California

The variations in trace element abundances of a suite of alkali-olivine basalts from the Big Pine volcanic field, California, have been ‘inverted’ following the method of Hofmann and co-workers to obtain source concentration and distribution coefficient data. The high Mg-numbers and ne-normative mineralogy of these lavas allow a simple correction to be made for fractional crystallisation, and together with a limited range in ⁸⁷Sr/⁸⁶Sr (0.7056–0.7064), suggest derivation from a relatively homogeneous source region. Negative correlations between SiO₂ and P₂O₅, and SiO₂ and Rb in the calculated primary magmas imply that both major and trace elements vary in a coherent fashion as a function of the degree of partial melting. The Big Pine lavas are characterised by high ratios of large-ion lithophile to high-field strength elements (Ba/Nb>60), and the inverse procedure demonstrates that this reflects source concentrations, as opposed to a mineralogical control. The calculated mantle source is further characterised by generally high abundances of Sr, Ba, K, and Th relative to Nb and Ta which imply that incompatible element enrichment of the source occurred above a subduction zone. A model Sm/Nd age of 1.8 Ga for this enrichment coincides with the regional crustal formation age. Such features imply that both the major and trace element components of the Big Pine lavas are derived from within lithospheric mantle, perhaps mobilised by the high geothermal gradients which characterise the extensional environment of the Basin and Range Province. A comparison with other Cenozoic mafic lavas throughout the western United States suggests that a substantial proportion of the mantle lithosphere in this area has similar chemical characteristics to the source of the Big Pine lavas. If this is the case, then it implies that convergent margins represent an important tectonic environment for the formation of lithospheric mantle.     

Mafic magmas from Mount Baker in the northern Cascade arc,Washington: probes into mantle and crustal processes

Five mafic lava flows located on the southern flank of Mount Baker are among the most primitive in the volcanic field. A comprehensive dataset of whole rock and mineral chemistry reveals the diversity of these mafic lavas that come from distinct sources and have been variably affected by ascent through the crust. Disequilibrium textures present in all of the lavas indicate that crustal processes have affected the magmas. Despite this evidence, mantle source characteristics have been retained and three primitive endmember lava types are represented. These include (1) modified low-K tholeiitic basalt (LKOT-like), (2) typical calc-alkaline (CA) lavas, and (3) high-Mg basaltic andesite and andesite (HMBA and HMA). The Type 1 endmember, the basalt of Park Butte (49.3–50.3 wt% SiO₂, Mg# 64–65), has major element chemistry similar to LKOT found elsewhere in the Cascades. Park Butte also has the lowest overall abundances of trace elements (with the exception of the HREE), indicating it is either derived from the most depleted mantle source or has undergone the largest degree of partial melting. The Type 2 endmember is represented by the basalts of Lake Shannon (50.7–52.6 wt% SiO₂, Mg# 58–62) and Sulphur Creek (51.2–54.6 wt% SiO₂, Mg# 56–57). These two lavas are comparable to calc-alkaline rocks found in arcs worldwide and have similar trace element patterns; however, they differ from each other in abundances of REE, indicating variation in degree of partial melting or fractionation. The Type 3 endmember is represented by the HMBA of Tarn Plateau (51.8–54.0 wt% SiO₂, Mg# 68–70) and the HMA of Glacier Creek (58.3–58.7 wt% SiO₂, Mg# 63–64). The strongly depleted HREE nature of these Type 3 units and their decreasing Mg# with increasing SiO₂ suggests fractionation from a high-Mg basaltic parent derived from a source with residual garnet. Another basaltic andesite unit, Cathedral Crag (52.2–52.6 wt% SiO₂, Mg# 55–58), is an Mg-poor differentiate of the Type 3 endmember. The calc-alkaline lavas are least enriched in a subduction component (lowest H₂O, Sr/P_N, and Ba/Nb), the LKOT-like lavas are intermediate (moderate Sr/P_N and Ba/Nb), and the HMBA are most enriched (highest H₂O, Sr/P_N and Ba/Nb). The generation of the LKOT-like and calc-alkaline lavas can be successfully modeled by partial melting of a spinel lherzolite with variability in composition of slab flux and/or mantle source depletion. The HMBA lavas can be successfully modeled by partial melting of a garnet lherzolite with slab flux compositionally similar to the other lava types, or less likely by partial melting of a spinel lherzolite with a distinctly different, HREE-depleted slab flux.     

An Archean arc basalt–Nb-enriched basalt–adakite association: the 2.7 Ga Confederation assemblage of the Birch–Uchi greenstone belt, Superior Province

The Uchi subprovince of the Archean Superior Province is a series of greenstone belts extending 600 km east–west along the southern margin of the North Caribou Terrane protocontinent. The 2.7 Ga Confederation tectonostratigraphic assemblage of the Birch–Uchi greenstone belt, northwest Ontario, is dominated by volcanic suites of mafic, intermediate and felsic composition. Tholeiitic basalts range compositionally from Mg# 59–26 evolving continuously to greater REE contents (La=2–19 ppm; Th/La_pm˜1), with small negative Nb anomalies. Primitive tholeiites are similar to modern intraoceanic arc basalts, whereas evolved members extend to greater concentrations of Ti, Zr, V, Sc, and Y, and lower Ti/Zr, but higher Ti/Sc and Ti/V ratios characteristic of back arc basalts. Calc-alkaline basalts to dacites are characterised by more fractionated REE (La/Yb_n=1–8), high Th/Nb_pm ratios and deeper negative Nb anomalies; they plot with modern oceanic arc basalts and some may qualify as high magnesium andesites. The two suites are interpreted as a paired arc–back arc sequence. A third group of Nb-enriched basalts (NEB; Nb=9–18 ppm) extend to extremely high TiO₂, Ta, P₂O₅, Sc and V contents, with strongly fractionated REE and ratios of Nb/Ta and Zr/Hf greater than primitive mantle values whereas Zr/Sm ratios are lower. The most abundant rhyolitic suite has extremely enriched but flat trace element patterns and is interpreted as strongly fractionated tholeiitic basalt liquids. A second group are compositionally similar to Cenozoic adakites and Archean high-Al, high-La/Yb_n tonalites; they possess Yb ≤ 0.4 ppm, Y ≤ 6 ppm and Sc ≤ 8 ppm, with La/Yb_n of 19–30 and Zr/Sm of 50–59. They are interpreted as melts of ocean lithosphere basaltic crust in a hot shallow subduction zone. Adakites are associated with NEB in Cenozoic arcs where there is shallow subduction of young and/or hot ocean lithosphere, often with oblique subduction. Slab melt adakites erupt, or metasomatise sub-arc mantle peridotite to generate an HFSE-enriched source that subsequently melts during induced mantle convection. The Archean adakite–NEB association erupted during development of the tholeiitic to calc-alkaline arc and its associated back arc. Their coexistence in the Confederation assemblage of the Birch–Uchi greenstone belt implies convergent margin processes similar to those in Cenozoic arcs. Received: 2 June 1999 / Accepted: 29 December 1999     

Plutonism in the Variscan Odenwald (Germany): from subduction to collision

 Latest Devonian to early Carboniferous plutonic rocks from the Odenwald accretionary complex reflect the transition from a subduction to a collisional setting. For ∼362 Ma old gabbroic rocks from the northern tectonometamorphic unit I, initial isotopic compositions (ε_Nd=+3.4 to +3.8;⁸⁷Sr/⁸⁶Sr =0.7035–0.7053;δ¹⁸O=6.8–8.0‰) and chemical signatures (e.g., low Nb/Th, Nb/U, Ce/Pb, Th/U, Rb/Cs) indicate a subduction-related origin by partial melting of a shallow depleted mantle source metasomatized by water-rich, large ion lithophile element-loaded fluids. In the central (unit II) and southern (unit III) Odenwald, syncollisional mafic to felsic granitoids were emplaced in a transtensional setting at approximately 340–335 Ma B.P. Unit II comprises a mafic and a felsic suite that are genetically unrelated. Both suites are intermediate between the medium-K and high-K series and have similar initial Nd and Sr signatures (ε_Nd=0.0 to –2.5;⁸⁷Sr/⁸⁶Sr=0.7044–0.7056) but different oxygen isotopic compositions (δ¹⁸O=7.3–8.7‰ in mafic vs 9.3–9.5‰ in felsic rocks). These characteristics, in conjunction with the chemical signatures, suggest an enriched mantle source for the mafic magmas and a shallow metaluminous crustal source for the felsic magmas. Younger intrusives of unit II have higher Sr/Y, Zr/Y, and Tb/Yb ratios suggesting magma segregation at greater depths. Mafic high-K to shoshonitic intrusives of the southern unit III have initial isotopic compositions (ε_Nd=–1.1 to –1.8;⁸⁷Sr/⁸⁶Sr =0.7054–0.7062;δ¹⁸O=7.2–7.6‰) and chemical characteristics (e.g., high Sr/Y, Zr/Y, Tb/Yb) that are strongly indicative of a deep-seated enriched mantle source. Spatially associated felsic high-K to shoshonitic rocks of unit III may be derived by dehydration melting of garnet-rich metaluminous crustal source rocks or may represent hybrid magmas. Received: 7 December 1998 / Accepted: 27 April 1999     

Source and tectonic implications of tonalite-trondhjemite magmatism in the Klamath Mountains

 In the Klamath Mountains, voluminous tonalite-trondhjemite magmatism was characteristic of a short period of time from about 144 to 136 Ma (Early Cretaceous). It occurred about 5 to 10 m.y. after the ∼165 to 159 Ma Josephine ophiolite was thrust beneath older parts of the province during the Nevadan orogeny (thrusting from ∼155 to 148 Ma). The magmatism also corresponds to a period of slow or no subduction. Most of the plutons crop out in the south-central Klamath Mountains in California, but one occurs in Oregon at the northern end of the province. Compositionally extended members of the suite consist of precursor gabbroic to dioritic rocks followed by later, more voluminous tonalitic and trondhjemitic intrusions. Most plutons consist almost entirely of tonalite and trondhjemite. Poorly-defined concentric zoning is common. Tonalitic rocks are typically of the low-Al type but trondhjemites are generally of the high-Al type, even those that occur in the same pluton as low-Al tonalite. The suite is characterized by low abundances of K₂O, Rb, Zr, and heavy rare earth elements. Sr contents are generally moderate (∼450 ppm) by comparison with Sr-rich arc lavas interpreted to be slab melts (up to 2000 ppm). Initial ⁸⁷Sr/⁸⁶Sr, δ ¹⁸O, and ɛ _Nd are typical of mantle-derived magmas or of crustally-derived magmas with a metabasic source. Compositional variation within plutons can be modeled by variable degrees of partial melting of a heterogeneous metabasaltic source (transitional mid-ocean ridge to island arc basalt), but not by fractional crystallyzation of a basaltic parent. Melting models require a residual assemblage of clinopyroxene+garnet±plagioclase±amphibole; residual plagioclase suggests a deep crustal origin rather than melting of a subducted slab. Such models are consistent with the metabasic part of the Josephine ophiolite as the source. Because the Josephine ophiolite was at low T during Nevadan thrusting, an external heat source was probably necessary to achieve significant degrees of melting; heat was probably extracted from mantle-derived basaltic melts, which were parental to the mafic precursors of the tonalite-trondhjemite suite. Thus, under appropriate tectonic and thermal conditions, heterogeneous mafic crustal rocks can melt to form both low- and high-Al tonalitic and trondhjemitic magmas; slab melting is not necessary. Received: 1 September 1994 / Accepted: 28 August 1995     

Significance of rare hydrous alkaline melts in Hawaiian xenoliths

 Two types of melt pockets occur in Hawaiian mantle xenoliths: amphibole-bearing (AMP) and spinel-bearing (SMP). AMPs contain amphibole (kaersutite), olivine (Fo₉₂), clinopyroxene (with 7–11% Al₂O₃), vesicles and glass. SMPs contain olivine, clinopyroxene, spinel, glass, and vesicles. The glasses in SMPs (SiO₂=44–45%, 11–12% alkalis, La=90–110 ppm) and AMPs (SiO₂=49–54%, 6–8.5% alkalis, La=8–14 ppm) are distinct in color and composition. Both glasses are generally characterized by LREE-enriched (chondrite-normalized) patterns. Amphibole and clinopyroxene have gently convex upward-to-moderately LREE-enriched patterns. Mineral/glass trace element abundance ratio plots show a strong negative Ti anomaly and a gentle negative Zr anomaly for clinopyroxene/glass; whereas amphibole/glass patterns show a distinctive positive Ti spike. The amphibole/glass trace element ratios are similar to published megacryst/lava values. An earlier study showed that the Hawaiian spinel lherzolites (lithosphere) have largely been metasomatized during post-erosional Honolulu magmatic activity. REE abundances of SMP glasses (melts) overlap the REE abundances calculated for such metasomes. The occurrence of hydrous, alkaline, mafic melt pockets in Hawaiian upper mantle xenoliths implies that (1) such hydrous liquids are generated in the upper mantle, and (2) water plays a role in magmatic activity associated with the Hawaiian plume. Although we are uncertain about the source (plume, lithosphere, or asthenosphere) of this water, we speculate that such melts and other alkalic lavas erupted on Oahu and on the sea-floor over the Hawaiian arch were generated from a broad „wet“ rim of a radially layered Hawaiian plume, whose hot and „dry“ core supplied the shield-forming magmas. Received: 6 February 1995 / Accepted: 28 August 1995     

Magma genesis and crustal contamination of continental intraplate lavas in northwestern Syria

The Miocene to Quaternary lavas of northwestern Syria range from basanite, alkali basalts, and tholeiites to basaltic andesites, hawaiites, and mugearites. Crustal assimilation and fractional crystallization processes (AFC) modified the composition of the mantle derived magmas. Crustal assimilation is indicated by decreasing Nb/U (52.8–17.9) and increasing Pb/Nd (0.09–0.21) and by variable isotopic compositions of the lavas (⁸⁷Sr/⁸⁶Sr: 0.7036–0.7048, ¹⁴³Nd/¹⁴⁴Nd: 0.51294–0.51269, ²⁰⁶Pb/²⁰⁴Pb: 18.98–18.60) throughout the differentiation. Modeling of the AFC processes indicates that the magmas have assimilated up to 25% of continental upper crust. The stratigraphy of the lavas reveals decreasing degrees and increasing depths of melting with time and the strongly fractionated heavy rare earth elements indicate melt generation in the garnet stability field. Modeling of melt formation based on trace element contents suggests that 8–10% melting of the asthenospheric mantle source produced the tholeiites, whereas basanite and alkali basalts are formed by 2–4% melting of a similar source.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Chemical evolution, petrogenesis, and regional chemical correlations of the flood basalt sequence in the central Deccan Traps, India

The lava sequence of the central-western Deccan Traps (from Jalgaon towards Mumbai) is formed by basalts and basaltic andesites having a significant variation in TiO₂ (from 1.2 to 3.3 wt%), Zr (from 84 to 253 ppm), Nb (from 5 to 16ppm) and Ba (from 63 to 407 ppm), at MgO ranging from 10 to 4.2 wt%. Most of these basalts follow a liquid line of descent dominated by low pressure fractionation of clinopyroxene, plagioclase and olivine, starting from the most mafic compositions, in a temperature range from 1220° to 1125°C. These rocks resemble those belonging to the lower-most formations of the Deccan Traps in the Western Ghats (Jawhar, Igatpuri and Thakurvadi) as well as those of the Poladpur formation. Samples analyzed for⁸⁷Sr/⁸⁶Sr give a range of initial ratios from 0.70558 to 0.70621. A group of flows of the Dhule area has low TiO₂ (1.2–1.5 wt%) and Zr (84–105 ppm) at moderate MgO (5.2–6.2 wt%), matching the composition of low-Ti basalts of Gujarat, low-Ti dykes of the Tapti swarm and Toranmal basalts, just north of the study area. This allows chemical correlations between the lavas of central Deccan, the Tapti dykes and the north-western outcrops. The mildly enriched high field strength element contents of the samples with TiO₂ > 1.5 wt% make them products of mantle sources broadly similar to those which generated the Ambenali basalts, but their high La/Nb and Ba/Nb, negative Nb anomalies in the mantle normalized diagrams, and relatively high⁸⁷Sr/⁸⁶Sr, make evident a crustal input with crustally derived materials at less differentiated stages than those represented in this sample set, or even within the sub-Indian lithospheric mantle.     

Volcanism in the Vitim Volcanic Field, Siberia: Geochemical Evidence for a Mantle Plume Beneath the Baikal Rift Zone

The Baikal Rift is a zone of active lithospheric extension adjacentto the Siberian Craton. The 6–16 Myr old Vitim VolcanicField (VVF) lies approximately 200 km east of the rift axisand consists of 5000 km³ of melanephelinites, basanites, alkaliand tholeiitic basalts, and minor nephelinites. In the volcanicpile, 142 drill core samples were used to study temporal andspatial variations. Variations in major element abundances (e.g.MgO = 3·3–14·6 wt %) reflect polybaric fractionalcrystallization of olivine, clinopyroxene and plagioclase. ⁸⁷Sr/⁸⁶Sr_i(0·7039–0·7049), ¹⁴³Nd/¹⁴⁴Nd_i (0·5127–0·5129)and ¹⁷⁶Hf/¹⁷⁷Hf_i (0·2829–0·2830) ratiosare similar to those for ocean island basalts and suggest thatthe magmas have not assimilated significant amounts of continentalcrust. Variable degrees of partial melting appear to be responsiblefor differences in Na₂O, P₂O₅, K₂O and incompatible trace elementabundances in the most primitive (high-MgO) magmas. Fractionatedheavy rare earth element (HREE) ratios (e.g. [Gd/Lu]_n > 2·5)indicate that the parental magmas of the Vitim lavas were predominantlygenerated within the garnet stability field. Forward major elementand REE inversion models suggest that the tholeiitic and alkalibasalts were generated by decompression melting of a fertileperidotite source within the convecting mantle beneath Vitim.Ba/Sr ratios and negative K anomalies in normalized multi-elementplots suggest that phlogopite was a residual mantle phase duringthe genesis of the nephelinites and basanites. Relatively highlight REE (LREE) abundances in the silica-undersaturated meltsrequire a metasomatically enriched lithospheric mantle source.Results of forward major element modelling suggest that meltingof phlogopite-bearing pyroxenite veins could explain the majorelement composition of these melts. In support of this, pyroxenitexenoliths have been found in the VVF. High Cenozoic mantle potentialtemperatures (1450°C) predicted from geochemical modellingsuggest the presence of a mantle plume beneath the Baikal RiftZone. KEY WORDS: Baikal Rift; mafic magmatism; mantle plume; metasomatism; partial melting     

Geochemistry of highly-undersaturated ocean island basalt suites from the South Atlantic Ocean: Fernando de Noronha and Trindade islands

The volcanic rocks of the South Atlantic Ocean islands of Fernando de Noronha and Trindade comprise a diverse magmatic series ranging from nephelinites and basanites to phonolites and, on Fernando de Noronha, trachytes. All rock types are highly silica undersaturated with the exception of Fernando de Noronha trachytes_, and have high abundances of incompatible trace elements and strongly LREE (light rare earth element)-enriched REE patterns. Crystal fractionation of parental basanitic magmas produced evolved phonolites and trachytes which display severe trace-element fractionation, even among trace elements (Nb, Ta, Zr, Hf) which normally behave highly incompatibly during crystallisation of alkaline magmas. Moderately to highly evolved compositions develop strongly MREE (middle REE)-depleted REE patterns, and become increasingly depleted in elements such as Nb and, in particular, Ta. Ratios of Nb/Ta and Zr/Hf are highly fractionated in phonolites (60–65, 64–77 respectively in Fernando de Noronha phonolites) compared to ratios in basanites (14, 45 respectively). The compatibility of Nb, Ta, and the REE, and the strong fractionation of Nb/Ta and Zr/Hf ratios and the MREE, during crystallisation from basanite to phonolite are attributable to the crystallisation of small amounts (<5%) of sphene. Trace-element behaviour is relatively insensitive to the major phenocryst phases, and is controlled by minor phases in highly undersaturated alkaline suites. Incompatible trace-element ratios (e.g. La/Nb, Th/Ta) in nephelinites and basanites from Fernando de Noronha and Trindade are generally comparable with those in basaltic and hawaiitic OIB (ocean island basalt) lavas from other South Atlantic islands, but are distinct from those of Gough and Tristan da Cunha OIB. The mantle source for the highly undersaturated volcanism on Fernando de Noronha and Trindade is similar in trace-element characteristics to the typical OIB source which produces alkaline lavas with significant relative enrichment in Nb and Ta compared to other trace elements (as expressed by low La/Nb, Ba/Nb and Th/Ta ratios). The highly undersaturated nature of the magmas and the slight fractionation of some incompatible-element ratios (elevated Ba/Nb, Ba/Rb, Ba/Th etc.) is consistent with a smaller degree of melting of a typical OIB source, but with residual phlogopite in the source to account for significant K depletion and LIL-element fractionation.     

Zirconolite-bearing ultra-potassic veins in a mantle-xenolith from Mt. Melbourne Volcanic Field,Victoria Land,Antarctica

One mantle xenolith from a basanite host of the Mt. Melbourne Volcanic Field (Ross Sea Rift) is extraordinary in containing veins filled with leucite, plagioclase, clinopyroxene, nepheline, Mg-ilmenite, apatite, titaniferous mica, and the rare mineral zirconolite. These veins show extensive reaction with the dunitic or lherzolitic host (olivine+spinel+orthopyroxene+clinopyroxene). The reaction areas contain skeletal olivine and diopside crystals, plagioclase, phlogopite, aluminous spinel and ilmenite in a fine grained groundmass of aluminous spinel, clinopyroxene, olivine, plagioclase and interstitial leucite. The vein composition estimated from modal abundances and microprobe analyses is a mafic leucite-phonolite with high amounts of K, Al, Ti, Zr and Nb but low volatile contents. The melt is unrelated to the host basanite and was probably derived by smallscale melting of incompatible element-enriched phlogopite-bearing mantle material and must have lost most of its volatile content during migration, crystallization and reaction with the host dunite. While the veins are completely undeformed the dunitic host shows slight deformation. Vein minerals crystallized at high temperatures above 1000°C and pressures below 5 kbar according to the phase assemblage including leucite, nepheline and K-feldspar. Spinel/olivine geothermometry yielded 800–920°C for the re-equilibration of the host peridotite. Thus the xenolith must have been at shallow depth prior to and during the late veining event. Mantle material at shallow depths is consistent with rifting and the regional extreme displacement at the transition from the rifted Victoria Land Basin in the Ross Sea to the uplifted Trans-Antarctic Mountains.     

Geochemistry and Petrogenesis of the Proterozoic Bandal Mafic Rocks,Himachal Pradesh,NW Himalaya

The Proterozoic Bandal mafic rocks, exposed in Kullu-Rampur window, Lesser Himalaya, Himachal Pradesh, indicate two distinct (high-Ti and low-Ti) magma types. The high-Ti basalts are characterised by high-TiO₂ (> 2 wt%), Ti/Y, Ti/Zr, TiO₂/K₂O and low Rb/Sr ratios. They are enriched in high field strength (HFS) elements (Nb, Zr, Ti) relative to low field strength (LFS) incompatible elements (K, Rb). The low-Ti basalts are charactersied by low TiO₂ (< 2 wt%), Ti/Y, Ti/Zr and high Rb/Sr and Rb/Ba ratios. Quartz-normative composition, continental tholeiite characteristics with Nb/La less than 1 are some of the common factors of the two groups of the Bandal mafic rocks. The trace element concentrations and their ratios of the two groups of the basalts indicate that they have been derived from the asthenosphere at different depths, low-Ti at shallow and high-Ti at deeper levels. Some of the chemical features like low Mg #, Cr, Ni, high incompatible element concentrations (especially Ba), light rare earth element (LREE) enriched patterns point towards assimilation and fractional crystallisation (AFC) process which may have played a significant role in the generation of these basalts.Furthermore, the Bandal mafic rocks, apart from field settings, are geochemically similar to other Proterozoic mafic bodies like the Rampur volcanics, Mandi-Darla volcanics, Garhwal volcanics and Bhimtal-Bhowlai volcanics of the Lesser Himalaya. This widespread Proterozoic continental tholeiitic magmatism over an area of 170,000 km² in the Lesser Himalaya provides an evidence of plume activity in the region.     

The Neoproterozoic Kolet Um Kharit bimodal metavolcanic rocks, south Eastern Desert, Egypt: a case of enrichment from plume interaction?

Neoproterozoic metavolcanic rocks of Kolet Um Kharit (KUKh) in the southern Eastern Desert of Egypt have been traditionally regarded as a bimodal island-arc sequence. However, geological and geochemical arguments presented here make this interpretation doubtful. Geochemically, these rocks are classified into mafic (tholeiitic basalts) and felsic (high-K rhyodacites to rhyolites) groups. Both the KUKh mafic and felsic metavolcanic rocks show similar geochemical characteristics, implying a genetic link. They have comparable trace element ratios, such as Zr/Nb (27–30 vs. 20–36), Y/Nb (5.44–6.25 vs. 5.05–5.9), K/Rb (577–1164 vs. 573–937), Ba/La (4.29–25–9 vs. 11.4–16.2), Nb/Yb (1.82–2.03 vs. 1.76–1.99). Similarly both groups have parallel LREE-enriched patterns (La/Yb_CN=2.37–2.81 vs. 2.55–3.17); and negative Nb and Ta anomalies (Nb/La_pm=0.51–0.58 vs. 0.45–0.52 and Ta/La_pm=0.51–0.62 vs. 0.49–0.55). The observed negative Nb and Ta anomalies in the KUKh metavolcanic rocks cannot be attributed to crustal contamination or fractional crystallization. These rocks could represent either a remnant of break-up LIP or were derived from an enriched mantle source containing subduction components beneath an intraoceanic back-arc basin. The recognition of the KUKh rocks as derived from an enriched mantle source revives interest in models that involve enrichment from “plume” interaction during the evolution of the Arabian-Nubian Shield.