Isotopic and chemical investigations on Angra dos Reis

We report on extensive isotopic studies of Pb, Sr and Xe and on chemical abundance measurements of K, Rb, Sr, Ba, Nd, Sm, U and Th for total meteorite and mineral separates of the Angra dos Reis achondrite. U-Pb, Th-Pb and Pb-Pb ages are concordant at 4.54 AE for the total meteorite and for high-purity whitlockite in Angra dos Reis. This establishes Angra dos Reis as an early planetary differentiate which has not been disturbed for these systems since 4.54 AE ago. Measured⁸⁷Sr/⁸⁶Sr in pyroxene and whitlockite for Angra dos Reis (ADOR) are distinctly below BABI by two parts in 10⁴ and only one part in 10⁴ above the lowest⁸⁷Sr/⁸⁶Sr (ALL) measured in an Allende inclusion. The difference in ADOR-ALL corresponds to an interval of condensation in the solar nebula of ～3 m.y. If²⁶Al was the heat source for the magmatism on the parent planets of Angra dos Reis and the basaltic achondrites (BABI) then the relatively large difference in⁸⁷Sr/⁸⁶Sr, BABI - ALL, must be the result of planetary evolution rather than condensation over ～10 m.y. Xe isotopic measurements confirm the presence of large amounts of²⁴⁴Pu-produced fission Xe and show that²⁴⁴Pu was enriched in the whitlockite relative to the pyroxene by a factor of ～18. We present chemical element enrichment factors between the whitlockite and the fassaitic pyroxene in Angra dos Reis. The enrichment factors demonstrate close analogy between the rare earth elements and their actinide analogs. The enrichment factor for Pu is intermediate to the enrichment factors of Nd and Sm.     

Petrogenesis of anhydrous clinopyroxenite xenoliths and clinopyroxene megacrysts in alkali basalts from the Ganseong area of South Korea

Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO₂ abundances in spinels and high TiO₂ and Na₂O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.     

Paleomagnetism of samples from the axial zone of the Afar depression

We have studied SmNd systematics in pyroxene and phosphate mineral separates of Angra dos Reis. A pyroxene-phosphate internal isochron age ofT₂ = 4.55 ± 0.04AE is obtained, in excellent agreement with reported Pb-Pb ages.¹⁴²Nd/¹⁴⁴Nd ratios in pyroxene samples are systematically larger than those in phosphates by 6 parts in 10⁵. This variation is tentatively assigned to a radiogenic contribution from extinct¹⁴⁶Sm. Fission xenon components in pyroxene and phosphate separates are characterized by discrete ratios of fission/spallation and evidence is presented for a third ratio in celsian. It is shown that this characteristic is due to a close association of²⁴⁴Pu with the light REE. Computed ratios²⁴⁴Pu/Nd are the same in pyroxene and phosphate separates, but²⁴⁴Pu/²³⁸U and²⁴⁴Pu/²³²Th ratios are not. Taking the fission xenon retention age to be 4.55 AE, we obtain an abundance ratio²⁴⁴Pu/Nd= 1.5 × 10^?4 (or an atomic ratio²⁴⁴Pu/¹⁵⁰Nd= 1.6 × 10^?3) at this time and in the region of the solar system where the Angra dos Reis parent body formed. The exposure age of Angra dos Reis, as obtained by the⁸¹Kr-⁸³Kr method is55.5 ± 1.2m.y. Neutron capture during the 55.5-m.y. exposure to cosmic rays increased the ratio¹⁵⁰Sm/¹⁴⁹Sm in Angra dos Reis by 6 parts in 10⁴.     

Rare earth element abundances in rocks and minerals from the Fiskenaesset Complex,West Greenland

Rare earth element (REE) abundances determined by activation analysis in rocks, plagioclase and mafic separates from the Fiskenaesset Complex are presented together with data on major and trace elements in the minerals. The REE data for the rocks and plagioclases are distinct from those of many other anorthositic complexes and the abundances are some of the lowest recorded for plagioclase from terrestrial anorthosites. The bulk and trace element compositions of the Fiskenaesset plagioclases show a number of similarities to those of lunar plagioclases. The plagioclases show a positive Eu anomaly of about 10 and a depletion in the heavy REE relative to the light ones. The mafic separates are enriched in the heavy REE relative to the light ones, and show no Eu anomaly except in one sample with a positive anomaly not attributable to plagioclase contamination. It is estimated, from experimental partition coefficient data, that the REE pattern in the magma at an early stage of fractionation was La (17×) to Lu (0.7× chondrites) with a possible positive Eu anomaly. This highly fractionated REE pattern may be attributed to partial melting of a garnet-bearing source.     

Potassium-rich volcanic rocks of the Muriah complex, Java, Indonesia: Products of multiple magma sources?

The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe²⁺) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H₂O and H₂O/CO₂ mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.     

Bay of Islands ophiolite suite,Newfoundland: Petrologic and geochemical characteristics with emphasis on rare earth element geochemistry

Characteristic geochemical features of the ophiolite suite from the Bay of Islands Complex have been determined by major and trace element analyses of 13 rocks. Based on elements, such as rare earth elements (REE), whose abundances are relatively immobile during alteration and metamorphism, we find that (1) the pillow lavas and diabases are relatively depleted in light REE similar to most tholeiites occurring along spreading oceanic ridges, in back-arc basins and comprising the early phases of volcanism in island arcs; (2) the gabbros, composed of cumulate plagioclase and olivine with poikilitic clinopyroxene, have REE contents consistent with formation as cumulates precipitated from magmas represented by the overlying pillow lavas and diabases; (3) as in most harzburgites from ophiolites, the Bay of Islands harzburgite and dunite have relative REE abundances inconsistent with a genetic relationship to the overlying basic rocks — this inconsistency may be primary or it may result from late-stage alteration, contamination and/or metamorphism; (4) some Bay of Islands lherzolites have major and trace element abundances expected in the mantle source of the overlying basic rocks. Overall, the geochemical features of this Bay of Islands ophiolite suite are similar to those from Troodos and Vourinos, but these data are not sufficient to distinguish between different tectonic environments such as deep ocean ridge, small ocean basin or young island arc.     

Dunite channels within a harzburgite layer from the Horoman peridotite complex,Japan: Possible pathway for magmas

Two discordant dunite channels in a polished slab were collected from a harzburgite layer in the Horoman orogenic lherzolite massif, Hokkaido, Japan. The dunite channels show extreme grain‐size variations, and include very large olivine megacrysts up to 1.6 m long. Spinel‐rich pyroxenite veins or veinlets occasionally cross‐cut the olivine megacrysts. Mineral compositions differ between channels, and the mineral compositions and textures of the dunite channels and the host harzburgite suggest a replacive origin for the dunites. The Sr and Nd isotopic ratios of clinopyroxene separates from the pyroxenite veins in two dunite channels are different, but these ratios are generally similar to those of mid‐ocean ridge basalts. Assuming the channels formed by the through‐flow of melts, then the trace element compositions of the melts estimated from the clinopyroxenes are broadly similar. The melts have similar features such as enriched in incompatible elements and depleted in heavy rare earth elements, but there are differences in the depletions in Ti and Ba, indicating melts that were different but of similar origins. A Rb–Sr crystallization age (~ 52 Ma) was obtained for clinopyroxene–orthopyroxene pairs in a dunite channel and its host harzburgite. The distinctive dunite channels with megacrysts formed as a result of the through‐flow of mafic magma(s), and those magmas had trace and minor element contents that are indicative of contributions of a melt derived from subducted oceanic lithosphere.     

Petrogenesis of basalts from the project FAMOUS area: experimental study from 0 to 15 kbars

Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe²⁺) = 0.68;Ni= 232ppm;TiO₂ = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo₈₈), clinopyroxene (Wo₃₂En₆₀Fs₉), and orthopyroxene (Wo₅En₈₃Fs₁₂). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′_D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′_D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′_D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO₂ and Na₂O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′_d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.     

Studies of Brazilian meteorites: III. Origin and history of the Angra dos Reis achondrite

The Angra dos Reis meteorite fell in 1869 and is a unique achondrite. It is an ultramafic igneous rock, pyroxenite, with 93% fassaite pyroxene which has 15.7% Ca-Tschermak's molecule, plus calcic olivine (Fo_53.1; 1.3% CaO), green hercynitic spinel, whitlockite (merrillite), metallic Ni-Fe, troilite, as well as magnesian kirschsteinite (Ks_62.3Mo_37.7), within olivine grains, and celsian (Cs_90.2An_7.7Ab_1.7Or_0.4) which are phases reported in a meteorite for the first time, and plagioclase (An_86.0), baddeleyite, titanian magnetite (TiO₂, 21.9%), and terrestrial hydrous iron oxide which are phases reported for the first time in this meteorite. Petrofabric analysis shows that fassaite has a preferred orientation and lineation which is interpreted as being due to cumulus processes, possibly the effect of post-depositional magmatic current flow or laminar flow of a crystalline mush. The mineral chemistry indicates crystallization from a highly silica-undersaturated melt at low pressure. Since the meteorite formed as a cumulate, pyroxene crystals may have gravitationally settled from a melt which crystallized melilite first. Plagioclase would be unstable in such a highly undersaturated melt, and feldspathoids would be rare or absent due to the very low alkali contents of the melt. The presence of rare grains of plagioclase and celsian may be the result of late-stage crystallization of residual liquids in local segregations. Thus, the Eu anomaly in Angra dos Reis may be the result of pyroxene separation from a melt which crystallized melilite earlier, rather than plagioclase as previously suggested.     

High-pressure inclusions in tholeiitic basalt and the range of lherzolite-bearing magmas in the Tasmanian volcanic province

Spinel-lherzolite xenoliths have been found in olivine tholeiite near Andover in the Tasmanian Tertiary volcanic province. They show a high-pressure mineralogy of predominant olivine (Mg₉₀), with aluminous enstatite (Mg₉₀) and lesser aluminous diopside and chrome-bearing spinel, and resemble lherzolite xenoliths commonly found in undersaturated lavas. Such xenoliths are unusual in tholeiitic basalts and the occurrence directly attests to a mantle origin for at least some tholeiitic magmas.The lherzolites are accompanied by doleritic and pyroxenitic xenoliths and by olivine, orthopyroxene, clinopyroxene and plagioclase xenocrysts. If near-liquidus phases are represented amongst the xenocrysts, then the magnesian number of the host basalt and its xenocryst assemblage provisionally suggest a magma derived by more than 15–20% partial melting of mantle peridotite, before commencing xenocryst crystallisation at pressures between 8–13 kbar.With this new record, lherzolite-bearing lavas in Tasmania now cover an extremely wide compositional range, extending from highly undersaturated olivine melilitite to olivine tholeiite. They also include a considerable number of fractionated alkaline rocks that are only sparsely reported in the literature as lherzolite hosts. This latter group contains representatives of a previously suggested but unestablished alkaline fractionation series based on olivine nephelinite, viz. calcic olivine nephelinite → sodic olivine nephelinite → potassi-sodic olivine nephelinite → mafic nepheline benmoreite → mafic phonolite.Lherzolite and megacryst-bearing lavas are relatively more abundant in peripheral parts to the main basalt sequences in Tasmania. This suggests that they developed in fringing zones of less intense mantle melting which enhanced stagnation and fractionation of magmas within the mantle before eruption. Calculated crustal thicknesses under these areas suggest that the magmas were generated at pressures exceeding 6–11 kbar, with the Andover tholeiitic magma exceeding 9 kbar.     

Phosphate in Angra dos Reis: Structure and composition of the Ca3(PO4)2 minerals

Extraterrestrial calcium phosphates (“whitlockites”) have the anhydrous β-Ca₃(PO₄)₂ structure, which is different from that of hydrous terrestrial whitlockite. This has been confirmed by X-ray refinement of the structure of a phosphate from the achondrite Angra dos Reis. In the β-Ca₃(PO₄)₂ structure, there is one crystallographic site, Ca(IIA), which is half-occupied by calcium, and which seems to have an energetically unfavorable configuration; natural phosphates with this configuration (including Angra dos Reis) have composition Ca₁₉(Mg,Fe)₂(PO₄)₁₄. Stability of the structure is probably increased by substitution of Na for Ca in Ca(IIA) giving composition Ca₁₈ (Mg,Fe)₂Na₂(PO₄)₁₄, which occurs in chondrites; by vacancy of Ca(IIA), with rare earths and yttrium substituting for calcium in other sites for charge balance, giving composition Ca₁₆(Y,RE)₂(Mg,Fe)₂(PO₄)₁₄, found in lunar rocks; or by replacing Ca with hydrogen, giving composition Ca₁₈(Mg,Fe)₂H₂(PO₄)₁₄, which is terrestrial whitlockite. Lack of the favorable substitutions of Na, (Y, RE) or H in Angra dos Reis phosphate implies that these elements were relatively scarce in its environment of formation.     

Compositions of deep-sea ash layers derived from north pacific volcanic arcs: variations in time and space

Glass separates from 115 ash layers derived from the Kamchatkan (DSDP Site 192; 34 layers), the eastern Aleutian (DSDP Site 183; 56 layers) and the Alaska Peninsula (DSDP Site 178; 25 layers) volcanic arcs have been analyzed for up to 28 elements. In addition, the abundance and diversity of associated mafic phenocrysts have been evaluated. The resulting data set has made possible an evaluation of the late Miocene to Recent changes in composition of ashes derived from North Pacific volcanic arcs and of the factors controlling the evolution of highly siliceous magmas.We find no evidence for a general transition from arc tholeiite to calc-alkalic magma parentage of ashes derived from the volcanic arcs during the last 10 m.y., but instead find 0.1- to 0.5-m.y. intervals during which particular types of volcanism are prevalent. Most convincing is the transition from arc tholeiite to calc-alkalic for ashes derived from Kamchatka during the last 0.8 m.y., a change believed to be associated with a landward shift in the site of magma generation. Considered together, ashes derived from North Pacific volcanic arcs have been becoming more siliceous during the last 1.5 m.y. and may be associated with accelerated subduction during the same time interval.Hydrous phenocrysts (e.g., biotite) are typically associated with low-silica deep-sea ashes, but not with terrestrial volcanic rocks of comparable silica contents, suggesting the important role of water in the evolution of siliceous magma. REE patterns and relative abundances of mafic phenocrysts demonstrate the importance of fractional crystallization in controlling the evolution of highly siliceous arc magmas. REE increase with increasing silica, but become less concentrated in ashes with SiO₂ > 64%. Eu anomalies increase throughout the SiO₂ range. Initial fractionation is dominated by clinopyroxene and plagioclase with amphibole strongly influencing fractionation above 64% SiO₂.     

Geochemistry of some volcanic rocks from south-eastern sicily: Rare earth and other trace element distribution

Some trace element data for volcanic rocks found at different levels, from Tertiary to Holocene, in south-eastern Sicily (Iblean Plateau and Mt. Etna) are presented and discussed in the present paper in order to better the information about the origin and relationships of the various rock types. Four groups of volcanic rocks have been recognized on the basis of their major element chemistry: 1) low-K tholeiites, 2) associated alkali basalts to nephelinites of the Iblean Plateau (Upper Pliocene to Lower Pleistocene), 3) the basal subalkaline lavas of Mt. Etna, and 4) the alkalic suite rocks that make up the bulk of the volcano. The distribution of Rb, Sr, Ni, Cr, Co, Cu, REE, Th and Sc suggests:

1. an origin of the Iblean magmas by a different degree of partial melting of a Rb-poor and possibly slightly hetereogeneous mantle;
2. quite distinct source compositions for the Etnean magmas, relative to those of the Iblean area, on the basis of their Rb and Sr contents;
3. an origin of the alkalic rocks of Mt. Etna from independently generated magma(s) rather than by crystal fractionation of the Etnean subalkaline magmas or of a magma having the geochemical features of the Iblean alkali basalts; evidence for this is given by the distribution features of the incompatible elements showing an origin for these rocks from compositionally different parent magmas and/or an evolution under widely variable environmental conditions;
4. the primary character for the chemical differences observed in some of the Etnean subalkaline rocks that can be accounted for by different physico-chemical conditions at their source rather than by crystal fractionation processes.

     

A geochemical study of island-arc and back-arc tholeiites from the Scotia Sea

⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios, REE and selected minor and trace elements are presented and compared for present-day volcanic rocks in the Scotia Sea.Tholeiitic basalts from the South Sandwich Islands show widely ranging contents of some lithophile elements, e.g. K₂O (0.09–0.55%) and Rb (1.55–14.2 ppm), but fairly constant Na₂O and Sr. Total REE contents range from about 4–20 times chondritic abundances with significant light-REE depletion and both positive and negative Eu anomalies. The variations in minor and trace element abundances are consistent with low-pressure fractional crystallization of plagioclase and clinopyroxene but only minor amounts of olivine. The⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios of the parental magmas are thought be 0.7038–0.7039 and 0.51301–0.51314 respectively, and indicate derivation of at least some⁸⁷Sr from subducted ocean crust.The back-arc tholeiites in the Scotia Sea have lower⁸⁷Sr/⁸⁶Sr ratios (0.7028–0.7033), similar¹⁴³Nd/¹⁴⁴Nd ratios (0.51305) and are variably light-REE-enriched(Ce_N/Yb_N= 1.0–1.6). Total REE contents are comparable to those of the South Sandwich Islands tholeiites.     

Bimodal tholeiitic and mildly alkalic basalts from Bhir area,central Deccan Volcanic Province,India: Geochemistry and petrogenesis

Bimodal tholeiitic and mildly alkalic basalts occur near Bhir, in the central part of Deccan Volcanic Province (DVP). Major and trace element concentrations show that, of the ten flows, nine are tholeiitic and one is an alkalic basalt. The Bhir basalts have a wide range of chemical composition. Geochemical variations in the stratigraphic section define three distinct phases of evolution (zones 1 to 3). Crystal fractionation of plagioclase, clinopyroxene, olivine and Fe–Ti oxide expanded the compositional range. Low Mg#s (39–55), low concentrations of Ni and Cr and high Zr suggest the evolved nature of the Bhir basalts. Fractionation modeling suggests about 42% fractional crystallization.In spite of the dominant role of fractional crystallization in the evolution of Bhir basalts, some other processes must be sought to explain the chemical variations. Crustal contamination, magma mixing and degree of partial melting are suggested to explain the observed chemical variations. Resorption, reverse zoning and compositional bimodality in plagioclase phenocrysts indicate magma mixing. Samples of flows one and four suspected of being contaminated all have enriched SiO₂ and LILE (K, Rb, and Ba) contents and depletion in Ti and P, believed to be due to ‘granitic’ crustal contamination.As compared to tholeiitic basalts, the alkalic basalts are characterized by low SiO₂ and high TiO₂, Na₂O, K₂O and P₂O₅. Alkalic basalts are richer in LILE (Rb and Ba), HFSE (Nb, Zr, and Y) and REE than the tholeiitic basalts. The alkalic basalt occurrence is important from a petrogenetic point of view and also suggests that the sources of alkalic basalt magmas may be of variable ages under different parts of the DVP. Based on major, trace and rare earth element distributions it is suggested that asthenospheric mantle having affinities with the source of OIB was the source material of the magmas and the range in the composition of tholeiitic and alkalic basalts was probably controlled by different degrees of melting and/or inhomogeneities in the mantle source.     

Isotope geochemistry (Sr–Nd–Pb) and petrogenesis of leucite-bearing volcanic rocks from “Colli Albani” volcano, Roman Magmatic Province, Central Italy: inferences on volcano evolution and magma genesis

The “Colli Albani” composite volcano is made up of strongly silica-undersaturated leucite-bearing rocks. Magmas were erupted during three main periods, but a complex plumbing system dominated by regional tectonics channelled magmas into different reservoirs. The most alkali-rich magmas, restricted to the caldera-forming period (pre-caldera), are extremely enriched in incompatible trace elements and display more radiogenic Sr (⁸⁷Sr/⁸⁶Sr?=?0.71057–0.71067), with slightly less radiogenic Pb with respect to those of the post-caldera period. Post-caldera volcanic activity was concentrated in three different volcanic environments: external to the caldera, along the caldera edge and within the caldera. The post-caldera magmas produced melilite- to leucitite-bearing, plagioclase-free leucitites. In contrast to the pre-caldera lavas, they are characterised by lower incompatible trace element abundances and less radiogenic Sr (⁸⁷Sr/⁸⁶Sr?=?0.71006–0.71039). Magmas evolved through crystal fractionation plus minor crustal assimilation in a large magma chamber during the pre-caldera period. The multiple caldera collapses dissected and partially obliterated the early magma chamber. During the post-caldera stage, magmas were channelled through several pathways and multiple shallow-level magma reservoirs were established. A lithospheric mantle wedge previously depleted in the basaltic component and subsequently enriched by metasomatic slab-derived component is suggested as the mantle source of Colli Albani parental magmas. Two different parental magmas are recognised for the pre- and post-caldera stages. The differences may be related to the interplay between smaller degrees of melting for the pre-caldera magmas and more carbonate-rich recycled subducted lithologies in the post-caldera magmas.     

Crystal fractionation of the basalt comendite series of the mount Edziza volcanic complex, British Columbia: Major and trace elements

The Mount Edziza Volcanic Complex in north-central British Columbia includes a group of overlapping basaltic shields, salic composite volcanoes, domes and small calderas that range in age from 7.5 Ma to less than 2000 years B.P. The volcanic assemblage is chemically bimodal, comprising voluminous alkali olivine basalt and hawaiite, a salic suite of mainly peralkaline trachyte and comendite, plus a relatively small volume of intermediate rocks (trachybasalt, tristanite, mugearite, benmoreite). The complex is the product of five cycles of magmatic activity, each of which began with alkali olivine basalt and culminated with the eruption of salic magma. The regular chemical variation shown by almost 100 major- and trace-element analyses suggests a genetic lineage between the basic and salic members of each cycle. Least-squares mathematical modelling, indicates that the salic rocks (trachyte and comendite) have formed by fractionation of observed phenocryst and cumulate nodule mineral phases from a common alkali olivine basalt parent magma.Hawaiite is thought to be a cumulate rock, formed by partial fractionation and feldspar accumulation within rising columns of primary alkali olivine basalt. Fractionation leading from alkali olivine basalt through trachybasalt and trachyte to comendite is believed to have taken place where primary basalt became trapped in large crustal reservoirs. The early removal of olivine, clinopyroxene and plagioclase, leading to a trachytic residuum, and subsequent fractionation of mainly alkali feldspar, leading to the peralkaline end members, is consistent with major- and trace-element variation and with isotopic and REE data.The chemical diversity of the complex is attributed to its location over a zone of crustal extension where mantle-derived basalt, trapped in large high-level reservoirs, underwent prolonged fractionation.     

Rare earth element geochemistry of garnet lherzolite and megacrystalline nodules from minette of the Colorado plateau province

Mineral and whole-rock REE abundances in garnet lherzolite and megacrystalline nodules from The Thumb display broad correlations with major element compositions. Lherzolites with > 12 modal % clinopyroxene plus garnet (“high-CaAl lherzolites”) have relatively flat chondrite-normalized whole-rock REE patterns. Lherzolites poor in clinopyroxene and garnet (“low-CaAl lherzolites”) have lower HREE in clinopyroxenes and garnets and higher whole-rock LREE/HREE. It is concluded that the low-CaAl lherzolites may have undergone LREE metasomatism after depletion of the major element compositions by partial melting and that much of the garnet now present was originally dissolved in aluminous orthopyroxene. The high-CaAl lherzolites may be interpreted either as primordial mantle samples or as products of equilibration with very LREE-enriched liquids. The “megacrystalline” nodules are medium- to ultracoarse-grained intergrowths and megacrysts with mineral compositions similar to discrete nodule suites in kimberlites. The REE abundances of the megacrystalline minerals are consistent with an origin as cumulates from magma with extremely fractionated REE, similar to minette or kimberlite.The patterns of correlation of REE and major elements in this inclusion suite are similar to the patterns observed in the garnet lherzolite and discrete nodule suites of southern African kimberlites. Both of the subcontinental mantle provinces represented by these suites contain three distinct petrogenetic components: refractory garnet lherzolite enriched in LREE and depleted in HREE, fertile garnet lherzolite with generally chondritic REE abundances, and a suite of ultracoarse minerals precipitated from magma with extremely fractionated REE generally similar to the host magmas.     

Origin and ascent history of unusually crystal-rich alkaline basaltic magmas from the western Pannonian Basin

The last eruptions of the monogenetic Bakony-Balaton Highland Volcanic Field (western Pannonian Basin, Hungary) produced unusually crystal- and xenolith-rich alkaline basalts which are unique among the alkaline basalts of the Carpathian–Pannonian Region. Similar alkaline basalts are only rarely known in other volcanic fields of the world. These special basaltic magmas fed the eruptions of two closely located volcanic centres: the Bondoró-hegy and the Füzes-tó scoria cone. Their uncommon enrichment in diverse crystals produced unique rock textures and modified original magma compositions (13.1–14.2 wt.% MgO, 459–657 ppm Cr, and 455–564 ppm Ni contents). Detailed mineral-scale textural and chemical analyses revealed that the Bondoró-hegy and Füzes-tó alkaline basaltic magmas have a complex ascent history, and that most of their minerals (～30 vol.% of the rocks) represent foreign crystals derived from different levels of the underlying lithosphere. The most abundant xenocrysts, olivine, orthopyroxene, clinopyroxene, and spinel, were incorporated from different regions and rock types of the subcontinental lithospheric mantle. Megacrysts of clinopyroxene and spinel could have originated from pegmatitic veins/sills which probably represent magmas crystallized near the crust–mantle boundary. Green clinopyroxene xenocrysts could have been derived from lower crustal mafic granulites. Minerals that crystallized in situ from the alkaline basaltic melts (olivine with Cr-spinel inclusions, clinopyroxene, plagioclase, and Fe–Ti oxides) are only represented by microphenocrysts and overgrowths on the foreign crystals. The vast amount of peridotitic (most common) and mafic granulitic materials indicates a highly effective interaction between the ascending magmas and wall rocks at lithospheric mantle and lower crustal levels. However, fragments from the middle and upper crust are absent from the studied basalts, suggesting a change in the style (and possibly rate) of magma ascent in the crust. These xenocryst- and xenolith-rich basalts yield divers tools for estimating magma ascent rate that is important for hazard forecasting in monogenetic volcanic fields. According to the estimated ascent rates, the Bondoró-hegy and Füzes-tó alkaline basaltic magmas could have reached the surface within hours to few days, similarly to the estimates for other eruptive centres in the Pannonian Basin which were fed by “normal” (crystal and xenoliths poor) alkaline basalts.     

Angra dos Reis: Plutonium distribution and cooling history

The preatmospheric mass of Angra dos Reis is estimated to be about 80 kg, based on cosmic ray track densities of 1?3 × 10⁶ cm^?2 in feldspars, olivines, and pyroxenes. The²⁴⁴Pu-fission track densities in pyroxenes and adjacent olivine-feldspar track detectors, as well as in whitlockites and adjacent pyroxene-olivine detectors are about 20 and 280 × 10⁶ cm^?2 respectively. These values correspond exactly to the²⁴⁴Pu-fission xenon contents in the two minerals. This suggests an almost instantaneous cooling (>70 K per m.y.) of the Angra dos Reis material 4.55 b.y. ago. This fast cooling is the reason for a quantitative⁴He retention since that time. If the⁴He excess found in Angra dos Reis is a real effect, the source of this excess remains unknown.