Basalts from Madeira: A petrochemical contribution to the genesis of oceanic alkali rock series

Petrological and geochemical investigations have been conducted on the little studied Neogene basaltic rocks of the Madeiran Islands. The Madeiran suite of minor intrusives and lavas consists of parental, unusually soda rich, alkali olivine basalts with hawaiite, mugearite and essexite derivatives. Olivine and clinopyroxene are dominant phenocryst and cumulus nodule phases. Low pressure fractionation of the parental magma by precipitation of these minerals gave rise to the hawaiitic trend. That olivine settling precedes clinopyroxene in the fractionation process can be deduced from Ca and Ni variations in the analysed rocks and phenocryst separates. Late stage feldspar flotation in a hawaiitic derivative liquid led to extrusive mugearites and an intrusive essexite.Low K/Rb ratios in the Madeiran basalts (ave. 325) point to the influence of phlogopite rather than hornblende in the mantle melting zone. The primitive alkali olivine basalt magma is thought to have arisen by partial melting following water release from small amounts of phlogopite (no more than 1%) at mantle depths around 100 km. A deep level of magma generation is consistent with the low values of heat flow recorded in ocean basins. Many other oceanic alkali basalt provinces remote from ridge systems may have arisen in a similar way.     

Fluids and Melts in the Upper Mantle

This paper presents a direct study of the fluids and melts in the upper mantle by examining the fluid inclusions, melt inclusions and glasses trapped in the mantle lherzolite xenoliths entrained by Cenozoic alkali basalts (basanite, olivine-nephelinite and alkali-olivine basalt) from eastern China. The study indicates that the volatile components, which are dissolved in high-pressure solid mineral phases of mantle peridotite at depths, may be exsolved under decompressive conditions of mantle plume upwelling to produce the initial free fluid phases in the upper mantle. The free fluid phases migrating in the upper mantle may result in lowering of the mantle solidus (and liquidus), thereby initiating partial melting of the upper mantle, and in the meantime, producing metasomatic effects on the latter.     

Complex geometry of the Cenozoic magma plumbing system in the central Sahara,NW Africa

Topographic uplifts in the central Sahara occur in the Hoggar-Aïr and Tibesti-Gharyan swells that consist of Precambrian rocks overlain by Cenozoic volcanic rocks. The swells and associated Cenozoic volcanism have been related either to mantle plumes or to asthenospheric upwelling and to partial melting due to rift-related delamination along pre-existing Pan-African mega-shears during the collision between Africa and Europe. The Cenozoic volcanic rocks in the Hoggar generally range from Oligocene tholeiitic/transitional plateau basalts, which occur in the centre of the dome, to Neogene alkali basalts characterized by a decrease in their degree of silica undersaturation and an increase in their La/Yb ratios. The alkali basaltic rocks occur mainly along the margins of the dome and typically have less radiogenic Nd and Sr isotopic ratios than the tholeiitic/transitional basalts. The geochemistry of the most primitive basaltic rocks resembles oceanic island basalt (OIB) tholeiitic – in particular high-U/Pb mantle (HIMU)-type – and is also similar to those of the Circum-Mediterranean Anorogenic Cenozoic Igneous (CiMACI) province. These characteristics are consistent with, but do not require, a mantle plume origin. Geophysical data suggest a combination of the two mechanisms resulting in a complex plumbing system consisting of (a) at depths of 250–200 km, an upper mantle plume (presently under the Aïr massif); (b) between 200 and 150 km, approximately 700 km northeastward deflection of plume-derived magma by drag at the base of the African Plate and by mantle convection; (c) at approximately 150 km, the magma continues upwards to the surface in the Tibesti swell; (d) at approximately 100 km depth, part of the magma is diverted into a low S-wave velocity corridor under the Sahara Basin; and (e) at approximately 80 km depth, the corridor is tapped by Cenozoic volcanism in the Hoggar and Aïr massifs that flowed southwards along reactivated Precambrian faults.     

Petrology,volume and age relations of alkaline and saturated peralkaline volcanics from Terceira,Azores

Four volcanoes form Terceira, one of the islands of the Azores group; three contain both basaltic and peralkaline and one only peralkaline rocks. A recently active basaltic fissure zone trends NW-SE across the island.The rocks fall into the alkaline olivine basalt suite although some young basalts are of transitional affinity. The geochemistry shows two general basaltic series: 1) undersaturated, found in lavas of the oldest volcano and in some recent fissure zone basalts and hawaiites; 2) saturated, found in the younger basaltic lavas.Since the emergence of Terceira there has been a contemporaneity of basalt and salic peralkaline lavas. The younger rocks show a bimodal composition distribution, the most voluminous compositions being alkali olivine basalt and comendite with negligible volume in the benmoreite-trachyte range. Two processes appear viable for the derivation of voluminous oversaturated peralkaline rocks: 1) partial melting of upper mantle material giving small magma batches of contrasting composition or 2) fractionation from a transitional basaltic parental magma.Now at Department of Geology, Victoria University of Wellington, New Zealand.     

The petrology and geochemistry of the Azores Islands

Forty lavas from the Azores Islands have been analyzed for ⁸⁷Sr/⁸⁶Sr ratios, major elements, first transition series metals, and LIL elements. The samples belong to the alkali basalt magma series but range from transitional hy-normative basalts from Terceira to basanitoids from Santa Maria. Differentiated lavas include both typical trachytes and comenditic trachytes and comendites. Major and trace element concentrations define smooth trends on variation diagrams, and these trends can be related to phases crystallizing in the rocks. Systematic interisland differences are also apparent in these variation diagrams. LIL element concentrations in island basalts are roughly twice as high as those in tholeiites from the adjacent Mid-Atlantic Ridge which transects the Azores Plateau. ⁸⁷Sr/⁸⁶Sr ratios in lavas from 6 of the 9 islands range from 0.70332 to 0.70354, a range similar to that found in tholeiites from the Mid-Atlantic Ridge transect of the Azores Plateau. This suggests that lavas from these islands and this portion of the Mid-Atlantic Ridge may be derived from a similar source. However, lavas from the islands of Faial and Pico have ⁸⁷Sr/⁸⁶Sr ratios up to 0.70394 and ratios in Sao Miguel lavas range up to 0.70525, suggesting basalts from these islands are derived from a chemically distinct source. Differences in the average LIL element concentrations of the least fractionated ridge tholeiites from the Azores Plateau and alkali basalts from the islands result from differences in extent of partial melting and residual mineralogy. The alkali basalts are derived by roughly half as much melting as are the tholeiites. Trace element concentrations in Azores peralkaline lavas preclude their derivation by partial melting of peridotitic mantle or basaltic crust; rather the data suggest they are produced by fractional crystallization of a basaltic parent.     

Variation in the geochemistry of mantle sources for tholeiitic and calc-alkaline mafic magmas,Western Sunda volcanic arc,Indonesia

Quaternary lavas of the normal island-arc basalt—andesite—dacite association in the islands of Java and Bali range from those belonging to tholeiitic series over Benioff-zone depths of ～ 150 km to high-K calc-alkaline series over Benioff-zone depths of 250 km. More abundant and diverse calc-alkaline lavas are found over intermediate Benioff-zone depths. On average, basaltic lavas become slightly more alkaline (largely due to increased K contents) with increasing depth to the Benioff zone. Levels of incompatible minor and trace elements (K, Rb, Cs, Ba, Nb, U, Th, light REE) show a corresponding increase of almost an order of magnitude.Low average Mg-numbers (～ 0.52) and Ni and Cr abundances (15–25 and 35–60 ppm, respectively) of basaltic lavas suggest that few lavas representing primary mantle-derived magma compositions are present. Calculated primary basaltic magma compositions for most tholeiitic and calc-alkaline volcanic centres are olivine tholeiites with 15–30% ol. The single high-K calc-alkaline centre considered yielded transitional alkali olivine basalt—basanite primary magma compositions. These calculated magma compositions suggest that the percentage of mantle melting decreases with increasing depth to the Benioff zone (from >25 to <10%), while the corresponding depth of magma separation increases from ～ 30 to 60 km.Calculation of REE patterns for basaltic magmas on the basis of peridotitic mantle sources with spinel lherzolite, amphibole lherzolite or garnet lherzolite mineralogy, and model REE levels of twice chondritic abundances, indicates that change in the conditions of magma genesis alone cannot explain the observed change in light-REE abundances of basaltic lavas with increasing depth to the Benioff zone. Complementary calculations of the REE levels of mantle sources required to yield the average tholeiitic, calc-alkaline and high-K calc-alkaline basaltic magma indicate that light-REE abundances must increase from 2–3 to 7–8 times chondrites with increasing depth to the Benioff zone. The percentages of mantle melting favoured on REE evidence are lower than those indicated by major-element considerations.The observed variation in incompatible element geochemistry of mantle magma sources is thought to be related directly or indirectly to dehydration and partial-melting processes affecting subducted oceanic crust. The possible nature of this relationship is discussed.     

Primary basalts and magma genesis

Three Eocene lavas from Skye, NW Scotland, have been subjected to anhydrous experimental studies within their melting ranges at pressures up to 30 kb. Two of these, an olivine-phyric magnesian alkali basalt and a near-aphyric Mg-poor transitional basalt, appear to show four-phase points on their liquidi at high pressures which are thought to have genetic significance. From experimental and mineralogical evidence, the magnesian basalt is postulated to be a primary magma, erupted without significant compositional change from its genesis by slight partial melting of a relatively Fe-rich spinel lherzolite upper mantle at about 60 km depth. The liquid seems to have had a reaction relationship with Ca-poor pyroxene (pigeonite) in the residual lherzolite. Partial crystallization of batches of this magma, delayed during its ascent at depths of about 40 km, is thought to have given rise to the Mg-poor basaltic liquids. The third lava studied experimentally, a sparsely olivine-phyric hawaiite, does not have olivine on the liquidus in any part of its anhydrous P-T diagram and therefore cannot have been derived under anhydrous conditions from olivine-saturated sources. The mineralogy and chemistry of the lavas are used to support an hypothesis that the hawaiites are products of partial crystallization of pockets of basalt magma at depths approximating to the crust/ mantle boundary beneath Skye, with rising to sufficient values to make the residual liquids comparatively rich in normative feldspar. Finally, the genesis of all other Skye Eocene lavas is reviewed in the light of the new experimental data.     

Geochemistry and Petrogenesis of Three Series of Cenozoic Basalts from Southeastern China

Cenozoic basaltic volcanism in southeastern China was related to the lithospheric extension and asthenospheric upwelling at the eastern Eurasian continental margin. The cenozoic basaltic rocks from this region can be grouped into three different series: tholeiitic basalts, alkali basalts, and picritic-nephelinitic basalts. Each basalt series has distinctive geochemical features and is not derived from a common source rock by different degrees of partial melting or from a common parental magma by fractional crystallization. The mineralogy, petrography, and major and trace-element geochemistry of the tholeiites are similar to oceanic island basalts, implying that the mantle source for these Chinese continental tholeiites was similar to that of the oceanic island basalts—an asthenospheric mantle. The alkali basalts and picritic-nephelinitic basalts are enriched in incompatible trace elements, and their geochemical features can be interpreted as a result of partial melting of an enriched lithospheric mantle, or the mixing products of an asthenospheric magma with a component derived from an enriched lithospheric mantle through thermal erosion at the base of the lithosphere. But the lack of a transitional rock type and continuous variational trends among these basalts suggests that the mixing between asthenospheric magmas and lithospheric magmas probably was not significant in the petrogenesis of the basalts from SE China. Low-degree partial melting of enriched lithospheric mantle alone can account for the observed geochemical data from these basalts.     

The mineral chemistry and origin of xenoliths from the lavas of Anjouan,Comores Archipelago,Western Indian Ocean

Mineralogical data for xenoliths occurring as inclusions in the fissure erupted alkali basalts and the basanitic tuffs of Anjouan reveal three xenolith suites: 1) the lherzolites, 2) the dunites and wehrlites, 3) the gabbros and syenites. The dunite-wehrlite suite and the gabbro suite are shown to represent high-level cumulate sequences resulting from ankaramitic fractionation of the hy-normative shield-building lavas and cotecictic fractionation of the alkali basalt lavas respectively, whilst the syenitic xenoliths represent evolved high-level intrusions. Mineralogical and rare earth element (REE) data indicate that the most likely origin for the spinel lherzolite xenoliths is by extraction of a basaltic phase from spinel peridotite, leaving a light REE-poor spinel lherzolite residuum. REE models, constructed using model peridotite assemblages, imply that the hy-normative basalt lavas may be derived by partial melting of spinel peridotite at pressures of <20–25 kb leaving a residual lherzolite, and that the alkali basalt and basanite melts are formed by small degrees of melting of a garnet-peridotite source at pressures of >20–25 kb. The spinel lherzolite source for the hy-normative basalts has been accidentally sampled during explosive eruption of the alkali basalt and basanite magmas.     

Studies of melt inclusions in some basalts from eastern China

Cenozoic basalts widespread in eastern China constitute an important sector of the circum-Pacific Cenozoic basalt belt. Basalt samples were collected from Wudalianchi (Heilongjiang Province), Nushan (Anhui Province), Fangshan (Jiangsu Province), Zhuji (Zhejiang Province), and Mingxi(Fujian Province). These basalts, for the most part, belong to the alkali basaltic series, and partly to tholeiites. A variety of inclusions commonly occurs in the rock-forming minerals of these basalts. The physicochemical conditions of basalt formation in different areas have been reviewed in special reference to the inclusion data. Our studies have shown that there is a close relationship between the features of the inclusions and the physicochemical conditions of basalt formation, which can, therefore, be regarded as a guide to the mechanism of basaltic petrogenesis. The results of research in this aspect are presented in the present paper.     

Primary basalts and magma genesis

The Pliocene-Holocene lavas of the Snake River Plain, Idaho, U.S.A., have a bimodal composition range, consisting predominantly of basalts (olivine-tholeiites), with subordinate intercalated tholeiitic andesites but with very few analyses falling between these groups. The more-magnesian of the tholeiitic andesites contain more total Fe, alkalis, TiO₂ and P₂O₅ but less SiO₂ than the less-magnesian basalts. Derivation of the tholeiitic andesites from the basalts by low-pressure fractional crystallization or by major-element crustal contamination does not seem possible, although some minor-element exchange with ancient crust apparently has occurred. Two lavas, representative of the least-magnesian basalts and the most-magnesian tholeiitic andesites, respectively, have been subjected to anhydrous experimental studies within their melting ranges at pressures up to 35kb. Both appear to show four-phase points on their liquidi at about 8kb and these are thought to have genetic significance. Microprobe analyses of the interstitial glasses in partially-crystalline runs on the basalt between 8 and 12kb show that these reproduce all the characteristic features of the Snake River Plain most-magnesian tholeiitic andesites, notably their reduced Si-saturation. The compositions of the most Mg-rich Snake River Plain basalts are such that they may perhaps be primary magmas, produced by partial fusion of a relatively Fe-rich spinel-lherzolite upper mantle at 50 to 60km depth; a proposal which accords well with the geophysics of this currently-active region. Partial crystallization of batches of this magma, delayed during ascent within the crust at depths of about 30 km, is thought to have given rise to the tholeiitic andesites.     

Variations in andean andesite compositions and their petrogenetic significance

Three linear zones of active andesite volcanism are present in the Andes — a northern zone (5°N–2°S) in Colombia and Ecuador, a central zone (16°S–28°S) largely in south Peru and north Chile and a southern zone (33°S–52°S) largely in south Chile. The northern zone is characterized by basaltic andesites, the central zone by andesite—dacite lavas and ignimbrites and the southern zone by high-alumina basalts, basaltic andesites and andesites. Shoshonites and volcanic rocks of the alkali basalt—trachyte association occur at scattered localities east of the active volcanic chain,The northern and central volcanic zones are 140 km above an eastward-dipping Benioff zone, while the southern zone lies only 90 km above a Benioff zone. Continental crust is ca. 70 km in thickness below the central zone, but is 30–45 km thick below northern and southern volcanic zones. The correlation between volcanic products and their structural setting is supported by trace element and isotope data. The central zone andesite lavas have higher Si, K, Rb, Sr and Ba, and higher initial Sr isotope ratios than the northern or southern zone lavas. The southern zone high-alumina basalts have lower Ce/Yb ratios than volcanics from the other zones. In addition, the central zone andesite lavas show a well-defined eastward increase in K, Rb and Ba and a decrease in Sr.Andean andesite magmas are a result of a complex interplay of partial melting, fractional crystallization and “contamination” processes at mantle depths, and contamination and fractional crystallization in the crust. Variations in andesite composition across the central Andean chain reflect a diminishing degree of partial melting or an increase in fractional crystallization or an increase in “contamination” passing eastwards. Variations along the Andean chain indicate a significant crustal contribution for andesites in the central zone, and indicate that the high-alumina basalts and basaltic andesites of the southern zone are from a shallower mantle source region than other volcanic rocks. The dacite-rhyolite ignimbrites of the central zone share a common source with the andesites and might result from fractional crystallization of andesite magma during uprise through thick continental crust. The occurrence of shoshonites and alkali basalts eat of the active volcanic chain is attributed to partial melting of mantle peridotite distant from the subduction zone.     

Geochemistry, Mineralogy and Magmatic Evolution of the Basaltic and Trachytic Lavas from Gough Island, South Atlantic

The Gough Island lavas range from picrite basalt through tosodalite-bearing aegirine-augite trachyte. The basaltic lavasare predominantly nepheline normative alkali basalts, althougha group of hypersthene normative tholeiitic basalts does occur.The oldest lavas on the island, represented by the Lower Basaltseries, are approximately 1?0 m.y. old and the youngest arethe Upper Basalts with an age of {small tilde} 0?13 m.y. Relatively coherent variations are described by the basalticand trachytic lavas with respect to both bulk rock major andtrace element geochemistry and mineral chemistry, and quantitativepetrogenetic modelling suggests that most of the variation canbe attributed to crystal fractionation/accumulation processesacting on a number of geochemically distinct parental magmas.The Upper Basalts and Lower Basalts have (within the limitsof sampling) a relatively restricted composition compared tothe Middle Basalt series lavas, with the latter ranging frompicrite basalt through to trachyandesite. The picrite basaltsand coarsely pyroxene-olivine phyric basalts represent partialcumulates with varying proportions (up to 40 wt. per cent) ofaccumulated olivine and clinopyroxene. In contrast, the moderatelyphyric and aphyric/finely porphyritic lavas represent the productsof crystal fractionation with the most evolved lavas havingexperienced at least 40 per cent fractional crystallizationof clinopyroxene, olivine, plagioclase and minor Fe-Ti oxidesand apatite. The detailed abundance variations in these lavasindicate that a number of parental magma compositions have fractionatedto produce the overall variations in basalt geochemistry, andsome of the magmas have interacted through mixing processes. The trachytic lavas show a large range in trace element abundance,but have only a limited major element variation. Most of thisvariation can be attributed to extensive (up to 70 per cent)fractional crystallization of predominantly alkali feldsparwith minor clinopyroxene, olivine, biotite, titano-magnetiteand apatite. A number of genetically distinct trachytes canbe recognized which are probably not related to each other byany simple fractional crystallization process. The compositionof the least evolved trachytes can be adequately accounted forby relatively extensive (up to 60 per cent) fractionation ofthe more evolved Middle Basalt series lavas. The trace element and isotopic characteristics of primitiveGough Island basalts support the concept that the source region(s)giving rise to these lavas is extremely enriched in highly incompatibleelements relative to primordial or ‘undepleted’mantle of bulk earth composition. It is unlikely that the lavashave sampled undepleted mantle as might be suggested by thesimilarity of the Sr and Nd isotopic ratios to ‘bulk earth’values. Rather, a model is favoured whereby the lavas are derivedfrom previously enriched sub-oceanic mantle which was subsequentlyinvaded and further enriched, at some time prior to partialmelting, by melts or fluids highly enriched in incompatibleelements. The enrichment could have occurred as veining by smalldegree partial melts or by infiltration of metasomatic fluids.     

Origin of some magmas in oceanic and circum-oceanic regions

Partial melting experiments on spinel-lherzolite, a rock which probably occurs in relatively shallow parts of the oceanic upper mantle, demonstrate that alkali basaltic melt is formed at depths of at least 20 kbar whereas tholeiitic melt is formed at lower pressures (< 15 kbar) under anhydrous conditions. The specimen studied was a relatively iron-rich natural spinel-lherzolite (Fe/Mg+Fe=0.15) and the melts produced have ratios comparable to those obtained in basalts. Slight increase of degree of partial melting produces picritic melt over a wide pressure range. Under hydrous (water-excess) conditions, andesitic melt is produced by partial melting of the same natural spinel-lherzolite and a synthetic lherzolite. The melting experiments on two different abyssal tholeiites from the Mid-Atlantic Ridge suggest that the derivation of olivine tholeiite from a more mafic magma or a mantle peridotite (lherzolite) is possible, but is limited to depths shallower than 25 km under essentially anhydrous conditions, whereas plagioclase tholeiite may have been formed by fractional crystallization at depths of about 20 km in the presence of a small amount (～ 2 wt.%) of water.It is suggested that under mid-ocean ridges, partial melting of spinel-lherzolite at depths shallower than 60 km would produce olivine-tholeiitic magma, which differentiates at shallower levels (20–25 km) under either essentially anhydrous or hydrous (but vapor-absent) conditions to produce abyssal tholeiites of olivine-tholeiite type or plagioclase-tholeiite type. It may be also possible that the former olivine-tholeiite is generated by direct partial melting of plagioclase-lherzolite. Alkali basalts in the oceanic region may be generated at depths greater than 50 km by relatively small degree of partial melting. Along island arcs and continental margins, where the subduction zones probably exist, partial melting of lherzolite would take place in the presence of water that may be supplied by breakdown of hydrous minerals in the subducted oceanic crust, thereby producing andesitic magmas. High-alumina basalt magma could be produced by partial melting of the dehydrated oceanic crust in the subduction zone at depths between 40 and 60 km, where garnet is unstable above the solidus.     

Cross-arc geochemical variations in volcanic fields in Honduras C.A.: progressive changes in source with distance from the volcanic front

A geochemical traverse across Honduras reveals the heterogeneity of the mantle underneath Central America. Alkali basalts from Lake Yojoa (170 km behind the front) have low ⁸⁷Sr/⁸⁶Sr but high La/Yb, and elevated incompatible trace element abundances, consistent with derivation from a normal mid-ocean ridge basalt source mantle via low degrees of melting. These lavas lack evidence for an enriched source thought to be intermingled with normal mid-ocean ridge basalt source mantle beneath most of Central America. The amplitude of the subducted slab signature decreases smoothly with distance from the volcanic front. Lavas from Zacate Grande, the area nearest to the volcanic front (17 km behind the arc), display large ion lithophile element enrichment and high field strength element depletion indicating the involvement of subducted material in magma genesis. Components of subducted material are not evident in lavas from Lake Yojoa, the area furthest from the arc. Basalts and basaltic andesites from Tegucigalpa, 102 km behind the volcanic front, are geochemically intermediate between those of Lake Yojoa and Zacate Grande. The lavas from Tegucigalpa show a decreased influence of the subduction component, and are affected by assimilation-fractional crystallization processes at shallow depths. The gradual decrease in the subducted component from the volcanic front to Zacate Grande, Tegucigalpa and finally Lake Yojoa contrasts with the abrupt decrease documented for southeast Guatemala, the only other area in Central America where a cross-arc transect has been studied. Received: 1 July 1995 / Accepted: 16 July 1997     

Lithospheric control on late Cenozoic magmatism at the boundary of the Tuva-Mongolian Massif,Khubsugul area,northern Mongolia

Late Cenozoic lavas from the western wall of the Khubsugul rift trough were erupted within the Tuva-Mongolian Massif with a pre-Vendian basement, and the lavas in the eastern wall of the trough were erupted within Early Caledonian terranes. The composition of the lavas was determined to vary across the strike of the boundary of the Tuva-Mongolian Massif. The western wall of the trough is dominated by hawaiites and contains subordinate volumes of basanites and much lower amounts of olivine tholeiites and basaltic trachyandesites. The eastern wall contains, in addition to hawaiites, widespread olivine tholeiites and basaltic andesites with subordinate amounts of basaltic trachyandesites. The boundary zone contains practically all rock types (except basaltic andesites) in roughly equal proportions. The trace-element simulations of the partial melting processes demonstrates that the basaltic magmas were produced mainly by 0.5–5% partial melting of garnet lherzolite, with the probable mixing with partial melts derived from spinel lherzolite. The main factor controlling the compositional variations of the lavas was likely the variable depths of their derivation due to variations in the lithosphere thickness at the boundary of the Tuva-Mongolian Massif. Based on the assumption that the source of the magmas was relatively homogeneous and on the results of simulations with the use of experimental data on peridotite melting, we concluded that the asthenospheric sources of the basaltic magmas occurred at depths of 75 ± 10 km (24.6 ± 3.2 kbar) beneath the Tuva-Mongolian Massif and at 60 ± 12 km (20.1 ± 3.8 kbar) beneath the Early Caledonian terranes.     

Origin of basaltic magmas in the Mojave Desert area,California

The basaltic lavas erupted throughout the Mojave Desert are basanites (SiO₂<46%, normative nepheline>5%, and K₂O>1.5%), alkali-olivine basalts (SiO₂=46–48%; ne=0–5%; and K₂O=1.0–1.5%), and low-alumina, sub-alkaline basalts (SiO₂=48–51%; ne=0; K₂O<1.0%). One volcano, Pisgah Crater, erupted five times, with lava from each successive phase containing more silica and less potash than the one proceeding it. This compositional trend is the reverse of that expected from differentiation of a single alkalic magma, and therefore, may represent a succession of magmas tapped from a zone of continuing partial melting in the mantle.These lava compositions suggest that first melting was under high water pressure and was followed by relatively dry partial melting of gamet-orthopyroxene-clinopyroxene-olivine assemblages. The successive increase in silica and alkali decrease also requires that the partial melting zone move to shallower levels.All lavas sampled in the Mojave Desert area have compositions that can best be explained by the extraction of magma from such a rising melting zone, analogous to the mantle diapirs suggested by Green and Ringwood.     

Chemical Diversity of the Ueno Basalts, Central Japan: Identification of Mantle and Crustal Contributions to Arc Basalts

The Ueno Basalts of central Japan comprise a monogenetic volcaniccone complex that was active between 2·76 and 1·34Ma. Basalts were erupted at more than 14 centers scattered overa region 40 km in diameter. Alkali basalt was erupted first,followed by sub-alkaline basalt. Quasi-concentric expansionof eruption centers coinciding with uplift and with decreasingalkalinity of the lavas suggests that Ueno magmatism originatedfrom a mantle diapir as it mushroomed at the base of the lithosphere.Depleted asthenospheric mantle (alkali basalt), enriched lithosphericmantle (sub-alkaline basalt), and crustal components are identifiedas chemical end-members in the petrogenesis of the Ueno Basalts.Incompatible trace element abundances indicate that the Uenoalkali basalts are typical within-plate basalts, whereas thesub-alkaline basalts show strong affinities with normal arclavas. Sr–Nd–Pb isotopic compositions indicate thatthe mantle source of the alkali basalts was more depleted thanthat of the sub-alkaline basalts. About 7% melting of asthenosphericmantle in the garnet-lherzolite stability field produced theprimitive alkali basalts and 12% melting of spinel lherzolitewithin the subcontinental lithosphere produced the primitivesub-alkaline basalts. Isotopic compositions and fluid mobile/immobileelement ratios broadly covary with SiO₂ contents in the sub-alkalinesuite, and increasing silica content is associated with strongerEMII (Enriched Mantle II) isotope affinities and fluid mobileelement abundances. A progressive AFC (assimilation–fractionalcrystallization) model assuming assimilation of a low-K silicicmelt reproduces the chemical variations observed in the sub-alkalinesuite. Melting of a flattening mantle diapir at the base ofthe lithosphere is the dominant cause of Ueno magmatism, accompaniedby the assimilation of older arc crust. KEY WORDS: arc basalt; crustal assimilation; mantle heterogeneity; Ueno Basalts     

华北晚中生代和新生代玄武岩中单斜辉石巨晶来源及其对寄主岩岩浆过程的制约:以莒南和鹤壁为例

本文对华北克拉通晚中生代和新生代碱性玄武质岩石中的单斜辉石巨晶进行了主、微量元素和Sr-Nd同位素的综合研究,发现晚中生代和新生代单斜辉石巨晶存在明显的主、微量元素和同位素组成上的差异。新生代单斜辉石巨晶有Al-普通辉石和次透辉石两类;而中生代单斜辉石巨晶只有Al-普通辉石。新生代单斜辉石SiO_2含量高、REE配分型式为上凸型、LILE和放射性元素含量高,并具有比寄主碱性玄武岩更亏损的Sr和Nd同位素组成;而中生代单斜辉石SiO_2含量低、REE配分型式为LREE富集型、LILE和部分HFSE以及放射性元素含量低,并具有比寄主碱性玄武岩稍富集的Sr和Nd同位素组成;巨晶的结构、矿物成分和地球化学特征,以及Mg-Fe在熔体与单斜辉石间的分配状况皆说明,新生代碱性玄武岩中单斜辉石巨晶是碱性玄武岩浆在高压下结晶的,因此二者是同源的;而中生代单斜辉石巨晶是被寄主岩浆偶然捕获的捕虏晶,是不同源的。华北新生代单斜辉石巨晶存在于碱性玄武岩和拉斑玄武岩中,它们具有比寄主碱性玄武岩更亏损的Sr和Nd同位素组成,说明即使是碱性玄武岩也不能完全代表软流圈来源的原始岩浆,其在上升过程中或多或少存在同位素组成富集的物质的混入。同时,拉斑玄武岩不是碱性玄武质岩浆直接结晶分异的产物,亦不是完全由部分熔融程度的不同造成的。拉斑玄武岩中存在岩石圈地幔物质的贡献或是岩浆房内碱性玄武质岩浆受地壳混染作用的结果。     

High-titania alkali-olivine basalts of north-central Oregon,U.S.A.

In north-central Oregon numerous small flows of alkali-olivine basalt occur in the Oligocene to early Miocene John Day Formation. Chemically, these basalts are characterized by relatively low SiO₂ and K₂O and very high TiO₂ and iron. Fifteen analysed specimens (44 to 48 percent SiO₂) have an average of 3.6 percent TiO₂ and 15 percent total iron. The average composition of the Oregon basalts compares closely with the average hawaiite of the Hawaiian Islands, differing only in having slightly higher iron and slightly lower SiO₂ and total alkalis. Closely associated flows of trachyandesite and quartz latite are chemically related to the basalts and probably formed by differentiation of an alkali-olivine basalt magma.Typical basalt specimens have 10 to 15 percent of modal olivine, interstitial alkali feldspar, and abundant clay minerals and chlorophaeite. Textures are subophitic or intersertal and phenocrysts are rare. Plagioclase laths are slightly zoned and range in composition from An₆₈ to An₄₄. Purplish-brown titaniferous augite is the only pyroxene, and ilmenite is the dominant opaque mineral.Distinct differences in composition and age, and the lack of transitional varieties indicate that these basalts are unrelated to the younger Columbia River basalts. They presumably represent a separate parent magma of alkalic affinity that was generated independently within the mantle.