Petrogenetic Evolution of the Torfaj?kull Volcanic Complex, Iceland I. Relationship Between the Magma Types

The Torfaj?kull volcano, Iceland's largest silicic centre, issituated close to the junction of the active, southerly propagatingEastern Rift Zone and the South Eastern Zone, an older crustalsegment. This paper provides major, trace, and some Sr isotopedata on postglacial (<10000 y) rocks, i.e., tholeiitic magmasof the Eastern Rift Zone and transitional basalts, icelandites,and rhyolites of the Torfaj?kull centre, and assesses the relationshipsbetween the magma types in terms of the development of the Icelandiccrust. Tholeiitic magmas from the Eastern Rift Zone are LILE-enrichedrelative to MORB. They have undergone extensive olivine-plagioclase-clinopyroxenefractionation at low pressures. Compared with the tholeiites,Torfaj?kull transitional basalts show LILE/HFS enrichment andhigher (⁸⁷Sr/⁸⁶Sr)₁ ratios. They define several magmatic lineagesand have equilibrated over a wide range of pressures. Both basalttypes were derived by very small degrees of partial meltingof compositionally similar mantle sources, the main differencebeing that the tholeiites were generated in the spinel Iherzolite,and the transitional basalts in the garnet lherzolite, stabilityfields, a conclusion previously reached by Meyer et al. (1985).The mantle sources may have contained LILE-enriched streaks. Low-pressure differentiation of Torfaj?kull transitional basaltproduced an iceiandite to sub-alkaline rhyolite sequence bycrystal fractionation, the rhyolites representing >90% crystallizationof parental basalts. The rhyolites were emplaced as nine separatelava fields, formed during 11 eruptive episodes. The compositionalrange within each field is limited, and, although similar, theranges define several magmatic lineages. Continued fractionationof plagioclase-alkali feldspar-clinopyroxene-magnetite-apatite-zirconassemblages generated peralkaline rhyolites in certain post-glacialeruptions. Chemical variations in the deposits from the Hrafntinnuskerperalkaline eruption were related predominantly to alkali feldsparfractionation, and the melts were erupted from a zoned magmachamber. All postglacial volcanic rocks at Torfajokull havebeen mantle derived and thus represent new additions to theIcelandic crust.     

Volcanic Rocks from the Nejapa and Granada Cinder Cone Alignments, Nicaragua, Central America

Mafic tholeiitic basalts from the Nejapa and Granada (NG) cindercone alignments provide new insights into the origin and evolutionof magmas at convergent plate margins. In comparison to otherbasalts from the Central American volcanic front, these marietholeiitic basalts are high in MgO and CaO and low in Al₂O_p,K₂O₁, Ba and Sr. They also differ from other Central Americanbasalts, in having clinopyroxene phenocrysts with higher MgO,CaO and Cr₂O₃ concentrations and olivine phenocrysts with higherMgO contents. Except for significantly higher concentrationsof Ba, Sr and ⁸⁷Sr/₈₆Sr, most of the tholeiites are indistinguishable in compositionfrom mid-ocean ridge basalts. In general, phenocryst mineralcompositions are also very similar between NG tholeiites andmid-ocean ridge basalts. The basalts as a whole can be dividedinto two groups based on relative TiO₂-K₂O concentrations. Thehigh-Ti basalts always have the lowest K₂O and Ba and usuallyhave the highest Ni and Cr. All of the basalts have experienced some fractional crystallizationof olivine, plagioclase and clinopyroxene. Relative to otherCentral American basalts, the Nejapa-Granada basalts appearto have fractionated at low P_T and P_H2O. The source of primarymagmas for these basalts is the mantle wedge. Fluids and/ormelts may have been added to the mantle wedge from hydrothermally-altered,subducting oceanic crust in order to enrich the mantle in Sr,Ba and ⁸⁷Sr/⁸⁶Sr, but not in K and Rb. The role of lower crustaicontamination in causing the observed enrichments in Sr, Baand ⁸⁷Sr/⁸⁶Sr of NG basalts in comparison to mid-ocean ridgebasalts, however, is unclear. Rutile or a similar high-Ti accessoryphase may have been stable in the mantle source of the low-TiNG basalts, but not in that of the high-Ti basalts. Mafic tholeiiticbasalts, similar to those from Nejapa and Granada, may representmagmatic compositions parental to high-Al basalts, the mostmafic basalts at most Central American volcanoes. The characterof the residual high-Al basalts after this fractionation stepdepends critically on P_H2O Both high and low-Ti andesites are also present at Nejapa. Likethe high-Ti basalts, the high-Ti andesites have lower K₂O andBa and higher Ni and Cr in comparison to the low-Ti group. Thehigh-Ti andesites appear to be unrelated to any of the otherrocks and their exact origin is unknown. The low-Ti andesitesare the products of fractional crystallization of plagioclase,clinopyroxene, olivine (or orthopyroxene) and magnetite fromthe low-Ti basalts. The eruption that deposited a lapilli sectionat Cuesta del Plomo involved the explosive mixing of 3 components:high-Ti basaltic magma, low-Ti andesitic magma and high-Ti andesiticlava.     

U-Th Disequilibrium and Rb-Sr Age Constraints on the Magmatic Evolution of Peralkaline Rhyolites from Kenya

Mildly peralkaline rhyolites of the Olkaria Volcanic Complex,located in the Kenyan sector of the East African rift valley,have low Sr concentrations and elevated Rb/Sr ratios (Sr 1·3–2ppm; ⁸⁷Rb/⁸⁶Sr = 748–1769) that potentially allow theresolution of time differences on the order of 1 ka by conventionalSr isotope determination. Because of their young eruption ages(     

The Arc Lavas of the Shirahama Group, Japan: Sr and Nd Isotopic Data Indicate Mantle-Derived Bimodal Magmatism

New Sr and Nd isotopic data are presented and integrated withprevious data for the Shirahama Group Mio-Pliocene medium-Kvolcanic are suite of south-central Honshu, Japan. Main resultsare: (1) The Shirahama lavas range in ⁸⁷Sr/⁸⁶Sr from 0.70315to 0.70337 and in ¹⁴³Nd/¹⁴⁴Nd from 0.51298 to 0.51306; the Srand Nd isotopic data cluster tightly within the mantle array,and all lie within an overlapping field of mid-ocean ridge basaltand ocean island basalt; (2) small differences exist among theShirahama tholeiitic series, calc-alkaline series and mixedlavas. The present isotopic data are consistent with a previouslypublished model, which proposes that chemical variations inmagmas of coexisting tholeiitic and calc-alkaline series areproduced through crystal fractionation from mantle-derived magmasof basalt and magnesian andesite, respectively. Moreover, thetholeiitic series and the calc-alkaline series are isotopicallyidentical. Thus, both magma series can be derived from a sourcemantle with the same isotopic composition, supporting the hypothesisof simultaneous generation of basalt and magnesian andesitemagmas from a single diapir rising through the mantle wedgeabove the subduction zone. The differences of water contentand temperature within the diapir are again thought to havebeen produced through dehydration and heating of an isotopicallyhomogeneous hydrous diapir. The isotopic data show that thehigh-SiO₂ lavas have the same isotopic compositions as moremafic lavas. These data and liquid lines of descent of the Shirahamamagmas suggest that even rhyolites can be produced by differentiationfrom mantle-derived magmas without crustal contamination. Analysesfrom 38 other arc volcanoes have been compiled to investigatethe intravolcano variability of ⁸⁷Sr/⁸⁶Sr. Twelve of these displayno intravolcano strontium isotopic variability, as is the casewith the Shirahama Group, but others show greater variationof ⁸⁷Sr/⁸⁶Sr from individual volcanic centers, presumably reflectingcrustal contamination. Most of the latter volcanoes are underlainby thick continental crust. It is noteworthy, however, thatthe greater variations of ⁸⁷Sr/⁸⁶Sr correlate with SiO₂ content;andesites or dacites, not basalts, from the same volcano havethe lowest ⁸⁷Sr/⁸⁶Sr, and these rocks are calc-alkaline in termsof FeO^*/MgO and SiO₂ Theoretically, assimilation of continentalcrust by the isotopically uniform Shirahama magmas could producethese relationships. Given that mantle-derived basalt and magnesianandesite both encounter continental crust on their ascent tothe surface, the hotter basalt magma would assimilate more crustalwallrocks than the cooler andesite, resulting in the basaltbeing more radiogenic. Fractional crystallization, magma mixing,and/or assimilation-fractional crystallization of these magmasin crustal magma chambers could produce large compositionalvariations, but the derivatives of the hotter basaltic magmas(tholeiitic series in the broad sense) would display greatercontamination than those derived from the cooler andesitic magmas(calc-alkaline series). ^*Telephone: 81-858-43-1215. Fax: 81-858-43-2184. e-mail: tamura{at}misasa.okayam-u.ac.jp     

Early Cretaceous Basaltic and Rhyolitic Magmatism in Southern Uruguay Associated with the Opening of the South Atlantic

The Early Cretaceous volcanic rocks of southern Uruguay comprisemafic and felsic volcanics. The position of these outcrops atthe southern edge of the Paraná–Etendeka continentalflood basalt province provides an opportunity to investigatepossible lateral variations in both mafic and more evolved rocktypes towards the margins of such an area of plume-related magmatism.The mafic lavas are divided into two compositionally distinctmagma types. The more voluminous Treinte Y Trés magmatype is similar to the low-Ti basalts of the Paraná floodbasalt province. The Santa Lucía magma type is a distinctand rare basalt type with ocean-island basalt type asthenosphericaffinities (high Nb/La, low ⁸⁷Sr/⁸⁶Sr_i). The felsic volcanicsare divided into two series, the Lavalleja Series and the AigüaSeries. The Lavalleja Series are chemically and isotopicallysimilar to the Paraná–Etendeka low-Ti rhyolites,and are considered to be related to the Treinte Y Tréslavas by extensive fractionation and crustal assimilation. TheAigüa Series have low ¹⁴³Nd/¹⁴⁴Nd_i and low ⁸⁷Sr/⁸⁶Sr_i andunlike the rhyolites of the Paraná, are interpreted asmelts of pre-existing mafic lower crust that subsequently underwentextreme fractionation. The differences observed in the felsicsuites may be linked to differences in the volumes of the associatedbasalts and the amounts of extension. KEY WORDS: South America; flood basalts; felsic volcanics; crustal melts; plume     

Strontium Isotope Geochemistry and Petrogenesis of the Early Tertiary Lava Pile of the Isle of Skye, Scotland, and other Basic Rocks of the British Tertiary Province: an Example of Magma--Crust Interaction

Most of the flows in the Palaeocene lava pile remnant of Skyeare members of the Skye Main Lava Series (SMLS), comprisingtransitional basalts and two associated suites of evolved lavas.The first suite evolves through Fe-rich hawaiites and mugearitesto benmoreites, and the second suite evolves through Fe-poorintermediates to trachytes. Ca-rich, alkali-poor olivine tholeiites(the Preshal Mhor magma type) occur as sparse flows in the stratigraphicallyhighest parts of the lava pile remnant and are abundant in thedyke swarm transecting it. Initial ⁸⁷Sr/⁸⁶Sr ratios rangingfrom 0.70308 to 0.70571 in 45 SMLS samples show no significantcorrelation with degree of zeolitization (H₂O⁺), silica saturation,or ⁸⁷Rb/⁸⁶Sr. A moderately good negative correlation with totalSr confirms published Pb-isotope evidence of interaction withancient, sialic crust. Details of the (⁸⁷Sr/⁸⁶Sr)_l versus Srpattern are consistent with previous hypotheses that the SMLSbasalt-benmoreite suite evolved at a depth near the Moho, whilstthe low-Fe trend to trachyte resulted from near-surface basaltfractionation. (⁸⁷Sr/⁸⁶Sr)_l values ranging from 0.70307 to 0.70621 for PreshalMhor basalts show a strong positive correlation with total Sr,consistent with a model of extensive fractionation within theupper crust of a mantle-derived low ⁸⁷Sr/⁸⁶Sr-low Sr magma,which became progressively contaminated with comparatively radiogeniccrustal Sr. The lowest measured (⁸⁷Sr/⁸⁶Sr)_l values of 0.70307and 0.70308, for a Preshal Mhor basalt and for an SMLS basaltrespectively, are consistent with the hypothesis that thesetwo magma types were produced by successive phases of partialmelting from a single volume of upper mantle. (⁸⁷Sr/⁸⁶Sr)_l values for additional miscellaneous basaltic lavas,dykes and major intrusives from Skye and from nearby Isle ofMull exhibit considerable variability within the range 0.7038to 0.7072, whilst three basaltic dykes from Northern Englandare in the range 0.7089 to 0.7123. The latter values overlapwith published (⁸⁷Sr/⁸⁶Sr)_l values for some of the granitesin the Tertiary Province of northwest Scotland and indirectlyremove objections based on Sr-isotopic arguments to the genesisof the granites by fractionation of basalt contaminated withcrustal Sr, but neither prove this nor disprove large-scalecrustal partial fusion.     

Evolution and Genesis of Magmas from Vico Volcano, Central Italy: Multiple Differentiation Pathways and Variable Parental Magmas

Vico volcano has erupted potassic and ultrapotassic magmas,ranging from silica-saturated to silica-undersaturated types,in three distinct volcanic periods over the past 0·5Myr. During Period I magma compositions changed from latiteto trachyte and rhyolite, with minor phono-tephrite; duringPeriods II and III the erupted magmas were primarly phono-tephriteto tephri-phonolite and phonolite; however, magmatic episodesinvolving leucite-free eruptives with latitic, trachytic andolivine latitic compositions also occurred. In Period II, leucite-bearingmagmas (⁸⁷Sr/⁸⁶Sr_initial = 0·71037–0·71115)were derived from a primitive tephrite parental magma. Modellingof phonolites with different modal plagioclase and Sr contentsindicates that low-Sr phonolitic lavas differentiated from tephri-phonoliteby fractional crystallization of 7% olivine + 27% clinopyroxene+ 54% plagioclase + 10% Fe–Ti oxides + 4% apatite at lowpressure, whereas high-Sr phonolitic lavas were generated byfractional crystallization at higher pressure. More differentiatedphonolites were generated from the parental magma of the high-Srphonolitic tephra by fractional crystallization of 10–29%clinopyroxene + 12–15% plagioclase + 44–67% sanidine+ 2–4% phlogopite + 1–3% apatite + 7–10% Fe–Tioxides. In contrast, leucite-bearing rocks of Period III (⁸⁷Sr/⁸⁶Sr_initial= 0·70812–0·70948) were derived from a potassictrachybasalt by assimilation–fractional crystallizationwith 20–40% of solid removed and r = 0·4–0·5(where r is assimilation rate/crystallization rate) at differentpressures. Silica-saturated magmas of Period II (⁸⁷Sr/⁸⁶Sr_initial= 0·71044–0·71052) appear to have been generatedfrom an olivine latite similar to some of the youngest eruptedproducts. A primitive tephrite, a potassic trachybasalt andan olivine latite are inferred to be the parental magmas atVico. These magmas were generated by partial melting of a veinedlithospheric mantle sources with different vein–peridotite/wall-rockproportions, amount of residual apatite and distinct isolationtimes for the veins. KEY WORDS: isotope and trace element geochemistry; polybaric differentiation; veined mantle; potassic and ultrapotassic rocks; Vico volcano; central Italy     

Sr Isotope and Trace Element Studies of the Great Dyke and Bushveld Mafic Phase and their Relation to Early Proterozoic Magma Genesis in Southern Africa

New Rb-Sr and trace element data are reported for the GreatDyke and Bushveld Mafic Phase layered intrusions. It is arguedthat geochemical characteristics, such as ⁸⁷Sr/⁸⁶Sr ratios andR.E.E. distribution patterns have been little modified by crustalcontamination. Rb-Sr data for whole-rocks of the Great Dyke yield an age of2514±16 m.y. and an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70261±4.Mineral data are consistent with these results. The low errorson the results indicate no significant variation of ⁸⁷Sr/⁸⁶Srratios of successive magmatic influxes emplaced in differentmagma chambers. Earlier Great Dyke magmas were highly Mg-richand represent extensive partial melts of the source material.One such influx is shown to have a high Rb/Sr ratio (0.25) anda fractionated R.E.E. pattern (Ce_N/YB_N 12). These ratios areconsidered to approximate those of the source region. The Bushveld Mafic Phase has been dated accurately for the firsttime and has a Rb-Sr age of 2095±24 m.y. Initial ⁸⁷Sr/⁸⁶Srratios increase in a stepwise manner upwards in the intrusionfrom 0.70563±2 to 0.70769±6. Each increase isabrupt and occurs at a horizon also characterized by a suddenirregularity in cryptic variation. The Mafic Phase was emplacedas a succession of magmatic influxes each of which had higher⁸⁷Sr/⁸⁶Sr ratio than its predecessor. The first magma was both Mg-rich (MgO 21.5 per cent) and SiO₂-rich(50–55 per cent SiO₂) and was derived by extensive partialmelting of a shallow level upper mantle source. This sourcewas characterized by trace element abundance ratios (e.g. Rb/Sr 0.25; K/Rb 90; Ce_N/Yb_N 11), similar to those of kimberlitesand some potassic lavas and comparable with those deduced forthe Great Dyke source region. It is postulated that when the Rhodesian and Kaapvaal cratonsstabilized, underlying refractory mantle became fixed theretoto form a proto-lithosphere. Shortly afterwards, at about 2800m.y. ago, this proto-lithospheric mantle was enriched by passagethrough it of fluids with kimberlitic trace element chemistry.This sub-cratonic mantle thereafter evolved with a relativelyhigh Rb/Sr ratio. Magmas derived from it have anomalous chemicalcharacteristics with respect to those of ocean-floor basalts,reflecting major differences in the evolution of their respectivesource regions.     

Crystal-Melt Separation and the Development of Isotopic Heterogeneities in Hybrid Magmas

If a magma is a hybrid of two (or more) isotopically distinctend-members, at least one of which is partially crystalline,separation of melt and crystals after hybridization will leadto the development of isotopic heterogeneities in the magmaas long as some of the pre-existing crystalline material (antecrysts)retains any of its original isotopic composition. This holdstrue whether the hybridization event is magma mixing as traditionallyconstrued, bulk assimilation, or melt assimilation. Once a magma-scaleisotopic heterogeneity is formed by crystal–melt separation,it is essentially permanent, persisting regardless of subsequentcrystallization, mixing, or equilibration events. The magnitudeof the isotopic variability resulting from crystal–meltseparation can be as large as that resulting from differentialcontamination, multiple isotopically distinct sources, or insitu isotopic evolution. In one model, a redistribution of one-thirdof the antecryst cargo yielded a crystal-enriched sample with⁸⁷Sr/⁸⁶Sr of 0·7058, whereas the complementary crystal-poorsample has ⁸⁷Sr/⁸⁶Sr of 0·7068. In other models, crystal-richsamples are enriched in radiogenic Sr. Isotopic heterogeneitiescan be either continuous (controlled by the modal distributionof crystals and melt) or discontinuous (when there is completeseparation of crystals and liquid). The first case may be exemplifiedby some isotopically zoned large-volume rhyolites, formed bythe eruptive inversion of a modally zoned magma chamber. Inthe latter case, the isotopic composition of any (for example)interstitial liquid will be distinct from the isotopic compositionof the bulk crystal fraction. The separation of such an interstitialliquid may explain the presence of isotopically distinct late-stageaplites in plutons. Crystal–melt separation provides anadditional option for the interpretation of isotopically zonedor heterogeneous magmas. This option is particularly attractivefor systems whose chemical variation is otherwise explicableby fractionation-dominated processes. Non-isotopic chemicalheterogeneities can also develop in this fashion. KEY WORDS: isotopic heterogeneity; zoning; hybrid magma; crystal separation; Sr isotopes; aplite; rhyolite     

Isotopic Composition of Strontium in Rocks of the Fen Alkaline Complex, South Norway

The isotopic composition of Sr and the abundances of Rb andSr have been determined in the alkaline rocks of the Fen Complex,South Norway. The ⁸⁷Sr/⁸⁸Sr ratios range from as low as 0.703in carbonatite (s?vite) to as high as 0.710 in rauhaugite. Thewhole rock analyses do not plot on a Nicolaysen diagram as anisochron. Calculation of the initial isotopic composition ofSr in the rocks at the time of intrusion of the complex, approximately550 m.y. ago, shows that the rocks are not simply related asthe differentiation products of a single magma, since they donot possess similar initial ⁸⁷Sr/⁸⁶Sr ratios. The lowest initialratio is seen in the s?vites and it is concluded that this rockrepresents the magma from which the other rocks of the complexwere derived. Production of hybrid rocks by bulk assimilationof granite gneiss in carbonatite is inadequate to account forthe observed Rb/Sr ratios. It is envisaged that selective concentrationof granitic Sr of high ⁸⁷Sr/⁸⁶Sr ratio together with loss orgain of variable amounts of Rb has taken place. The processis closely connected with the fenitization observed at the marginsof the complex and is of a metasomatic nature. Thus, the genesisof rocks of the melteigite-ijolite-urtite series may be consideredto be a rheomorphic process. The ⁸⁷Sr/⁸⁶Sr ratios observed inr?dberg and rauhaugite can be explained in terms of the metasomaticalteration of damtjernite.     

An Isotope and Trace Element Study of the East Greenland Tertiary Dyke Swarm: Constraints on Temporal and Spatial Evolution during Continental Rifting

Dykes of the East Greenland Tertiary dyke swarm can be dividedinto pre- and syn-break-up tholeiitic dykes, and post-break-uptransitional dykes. Of the pre- and syn-break-up dykes, themost abundant group (Tholeiitic Series; TS) has major elementcompositions similar to the main part of the East Greenlandflood basalts. A group of high-MgO tholeiitic dykes (Picrite–AnkaramiteSeries; PAS) are much less common, and are equivalent to someof the oldest lavas of the East Greenland flood basalts. Isotopiccompositions of the TS and PAS dykes partly overlap with thosefor Iceland, but Pb isotopic compositions extend to less radiogenicvalues than those seen in either Iceland or North Atlantic mid-oceanridge basalt (MORB). The isotopically depleted source requiredto account for this isotopic variation is interpreted as subcontinentallithospheric mantle with low ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb and high     

Evolution of Holocene Dacite and Compositionally Zoned Magma, Volcan San Pedro, Southern Volcanic Zone, Chile

Volcán San Pedro in the Andean Southern Volcanic Zone(SVZ) Chile, comprises Holocene basaltic to dacitic lavas withtrace element and strontium isotope ratios more variable thanthose of most Pleistocene lavas of the underlying Tatara–SanPedro complex. Older Holocene activity built a composite coneof basaltic andesitic and silicic andesitic lavas with traceelement ratios distinct from those of younger lavas. Collapseof the ancestral volcano triggered the Younger Holocene eruptivephase including a sequence of lava flows zoned from high-K calc-alkalinehornblende–biotite dacite to two-pyroxene andesite. Notably,hornblende–phlogopite gabbroic xenoliths in the daciticlava have relatively low ⁸⁷Sr/⁸⁶Sr ratios identical to theirhost, whereas abundant quenched basaltic inclusions are moreradiogenic than any silicic lava. The latest volcanism rebuiltthe modern 3621 m high summit cone from basaltic andesite thatis also more radiogenic than the dacitic lavas. We propose thefollowing model for the zoned magma: (1) generation of hornblende–biotitedacite by dehydration partial melting of phlogopite-bearingrock similar to the gabbroic xenoliths; (2) forceful intrusionof basaltic magma into the dacite, producing quenched basalticinclusions and dispersion of olivine and plagioclase xenocryststhroughout the dacite; (3) cooling and crystallization–differentiationof the basalt to basaltic andesite; (4) mixing of the basalticandesite with dacite to form a small volume of two-pyroxenehybrid andesite. The modern volcano comprises basaltic andesitethat developed independently from the zoned magma reservoir.Evolution of dacitic and andesitic magma during the Holoceneand over the past 350 kyr reflects the intrusion of multiplemafic magmas that on occasion partially melted or assimilatedhydrous gabbro within the shallow crust. The chemical and isotopiczoning of Holocene magma at Volcán San Pedro is paralleledby that of historically erupted magma at neighboring VolcánQuizapu. Consequently, the role of young, unradiogenic hydrousgabbro in generating dacite and contaminating basalt may beunderappreciated in the SVZ. KEY WORDS: Andes; dacite; gabbro; Holocene; strontium isotopes     

The Origin of Associated Basic and Acid Rocks in the Lebombo--Nuanetsi Igneous Province, Southern Africa, as implied by Strontium Isotopes

Whole rock Rb–Sr measurements were made on associatedbasic and acid intrusives and extrusives from the northern andsouthern ends of the Lebombo monocline with a view to determineif the acid rocks came from the mantle or from the crust. Inthe south, in Swaziland (now called Ngwame) and Zululand, rhyolitesand granophyres (age 202 14 m.y.) have an initial Si⁸⁷–Sr⁸⁶ratio of 0.7042 0.0005; in the north, in the Nuanetsi syncline,rhyolites (age 206 13 m.y.) and granites from ring complexes(age 177 7 m.y.) have initial ratios of 0.7081 0.0008 and0.7085 0.0007, respectively. The initial ratios of the basicrocks, basalts and gabbros, vary in both areas and have a rangefrom 0.7042 to 0.7125 which can be explained by crustal contamination.The low initial ratios and isotopic homogeneity of the acidmagmas over long distances (160 km) in Swaziland and Zululandare interpreted as implying that they were derived from themantle.     

Rb-Sr ages of Precambrian dolerite and alkaline dikes,southeast Mysore state,India

Rb-Sr isochron ages have been determined for two suites of Precambrian dikes in the Bidadi-Harohalli area of southeast Mysore State. Whole-rock samples of unmetamorphosed dolerites yield an age of 2420±246 (2σ) m.y., which is a minimum value for the intruded Peninsular Gneiss and Closepet Granite. The dolerite magma originated in the mantle, as indicated by the initial ⁸⁷Sr/⁸⁶Sr ratio of 0.7012±0.0010 (2σ). A suite of alkaline dikes, also referred to as felsite and feldspar porphyry dikes, has an age of 832±40 (2σ) m.y., which correlates with the intrusion of the Chamundi Hill Granite and the feldspar porphyry dikes near Srirangapatnam. One of the alkaline dikes has a K-Ar age of 810±25 m.y., indicating an absence of subsequent thermal events in the area.     

Kistufell: Primitive Melt from the Iceland Mantle Plume

This paper presents new geochemical data from Kistufell (64°48'N,17°13'W), a monogenetic table mountain situated directlyabove the inferred locus of the Iceland mantle plume. Kistufellis composed of the most primitive olivine tholeiitic glassesfound in central Iceland (MgO 10·56 wt %, olivine Fo_89·7).The glasses are interpreted as near-primary, high-degree plumemelts derived from a heterogeneous mantle source. Mineral, glassand bulk-rock (glass + minerals) chemistry indicates a low averagemelting pressure (15 kbar), high initial crystallization pressuresand temperatures (10–15 kbar and 1270°C), and eruptiontemperatures (1240°C) that are among the highest observedin Iceland. The glasses have trace element signatures (La_n/Yb_n<1, Ba_n/Zr_n 0·55–0·58) indicative ofa trace element depleted source, and the Sr–Nd–Pbisotopic ratios (⁸⁷Sr/⁸⁶Sr 0·70304–0·70308,¹⁴³Nd/¹⁴⁴Nd 0·513058–0·513099, ²⁰⁶Pb/²⁰⁴Pb18·343–18·361) further suggest a long-termtrace element depletion relative to primordial mantle. HighHe isotopic ratios (15·3–16·8 R/R_a) combinedwith low ²⁰⁷Pb/²⁰⁴Pb (15·42–15·43) suggestthat the mantle source of the magma is different from that ofNorth Atlantic mid-ocean ridge basalt. Negative Pb anomalies,and positive Nb and Ta anomalies indicate that the source includesa recycled, subducted oceanic crustal or mantle component. PositiveSr anomalies (Sr_n/Nd_n = 1·39–1·50) furthersuggest that this recycled source component involves lower oceaniccrustal gabbros. The     

Ultramafic Xenoliths in Plio-Pleistocene Alkali Basalts from the Eastern Transylvanian Basin: Depleted Mantle Enriched by Vein Metasomatism

Ultramafic xenoliths from alkali basalts in the Perjani Mountainsin the Eastern Transylvanian Basin (ETB) of Romania are mainlyspinel Iherzolites, although spinel harzburgites, websterites,clinopyroxenites and amphibole pyroxenites are also present.Amphibole veins cut some spinel peridotite samples. All arederived from the shallow lithospheric upper mantle. In general,textural variations are restricted to protogranular and porphyroclastictypes, compared with the more varied textures found in mantlexenoliths from the alkali basalts of the neighbouring PannonianBasin. Also, ETB peridotites are richer in amphibole. Thus,the mantle beneath the edge of the ETB is less deformed butmore strongly metasomatized than the mantle closer to the centreof the Pannonian Basin.Mineralogical and bulk-rock geochemicalvariations resemble those of spinel Iherzolites from other sub-continentalshallow mantle xenolith suites. There is no apparent correlationbetween deformation and geochemistry, and much of the majorand trace element variation is due to variable extraction ofpicritic melts. The REE patterns of separated clinopyroxenesfrom the peridotite xenoliths are mostly LREE depleted, althoughclinopyroxenes from regions adjacent to amphibole veins haveexperienced an enrichment in La and Ce and a change in theirSr and Nd isotopic values towards those of the vein, while stillretaining an overall LREE depletion. Clinopyroxenes from thewebsterites and clinopyroxenites are more variable. Amphibolein the hydrous pyroxenites and amphibole veins is strongly LREEenriched and is considered to be metasomatic in origin. ⁸⁷Sr/⁸⁶Srand ¹⁴³Nd/^l44Nd isotopic ratios of the xenoliths vary between07018 and 07044, and 051355 and 0 51275, respectively. Thesevalue are more depleted than those obtained for xenoliths fromthe Pannonian Basin. The lower ^l43Nd/^l44Nd and higher ⁸⁷Sr/Sr⁸⁶values are found in anhydrous pyroxenites, metasomatic amphibolesin veins and amphibole pyroxenites, and in the only exampleof an equigranular spinel Iherzolite in the suite.The ETB xenolithswere brought to the surface in alkaline vokanism which post-dateda period of Miocene to Pliocene subduction-related cak-alkalinevolcanism. However, the effects of the passage of either slab-derivedfluids or cak-alkaline magmas through the ETB lithospheric mantlecannot be discerned in the chemistry of the xenoliths. The metasomaticamphibole has ⁸⁷Sr/Sr⁸⁶ and ¹⁴³Sr/Sr¹⁴⁴ ratios similar to thehost alkali basalts, but the least evoked cak-alkaline magmasalso have similar Sr and Nd isotope compositions. The REE patternsof the amphibole resembk those of amphiboles considered to havecrystallized from alkaline melts. No preferential enrichmentin elements typically associated with slab-derivedfluids (K,Rb and Sr) relative to elements typically depleted in cak-alkalinemagmas (Ti, 2jr and Nb) has been observed in the vein amphiboles,although some interstitial amphibole is depleted in all incompatibletrace elements, including LREE. Thus, despite its position closeto the calc-alkaline volcanic arc of the Eastern Carpathians,we cannot readily detect any interaction between the lithosphericupper mantle beneath the ETB and subduction-related magmas orfluids. Metasomatism in the lithospheric mantle is instead largelyrelated to the passage of a primitive alkaline magma similarto the host alkali basal ^*corresponding author     

Distinguishing Melting of Heterogeneous Mantle Sources from Crustal Contamination: Insights from Sr Isotopes at the Phenocryst Scale, Pisgah Crater, California

Compositionally heterogeneous basaltic centers from a varietyof tectonic environments, including Pisgah Crater in the MojaveDesert region of California, exhibit secular changes in theirchemistry that might be explained by the sequential meltingof ultramafic to mafic mantle sources. We have analyzed phenocrystsfrom alkali basalts and hawaiites erupted at Pisgah Crater toinvestigate the effects of open-system modifications imposedon basaltic systems. We present ⁸⁷Sr/⁸⁶Sr data for individualphenocrysts of amphibole and clinopyroxene and the first publishedresults of single olivine grains, in addition to plagioclase.Each mineral phase exhibits a range in Sr isotope compositionthat may only partially overlap the isotopic composition ofthe other mineral phases, suggesting an interplay between twomagmatic end-members that continued up to the time of eruption.Limited ⁸⁷Sr/⁸⁶Sr variability in minerals from early and intermediatelavas indicates only moderate syn-crystallization open-systemmodification, whereas minerals in late-erupted lavas have muchhigher ⁸⁷Sr/⁸⁶Sr, consistent with extensive open-system modification.Rimward increases in ⁸⁷Sr/⁸⁶Sr of plagioclase confirm that thesechanges occurred within the stability field of plagioclase and,therefore, at crustal or near-crustal depths. The major elementcompositions of olivine-hosted melt inclusions indicate thatan Al-rich component of andesitic composition (⁸⁷Sr/⁸⁶Sr 0·7056),possibly derived from plagioclase-rich cumulates or pelites,was assimilated by magma generated from asthenosphere or younglithosphere with ⁸⁷Sr/⁸⁶Sr 0·7038. The results clearlydemonstrate the utility of measuring the ⁸⁷Sr/⁸⁶Sr of individualminerals and indicate that Pisgah Crater basalts probably acquiredisotopically enriched geochemical signatures from crustal contamination,rather than from mixing of heterogeneous mantle melts. KEY WORDS: assimilation; basalts; melt inclusions; minerals; Sr isotopes     

Petrology of the Cenozoic volcanism in the Upper Benue valley,northern Cameroon (Central Africa)

Thirty-one plugs of alkaline volcanic rocks of Cenozoic age (37 Ma in mean) occur in the Upper Benue valley, northern Cameroon (Central Africa). The complete alkaline series (alkaline basalts, hawaiites, mugearites, phonolites, trachytes and rhyolites) is represented. Basalts contain phenocrysts of olivine, Al-Ti-rich diopside, and Ti-magnetite, and hawaiites-abundant microphenocrysts of plagioclase. Mugearites have a trachytic texture and contain xenocrysts of K-feldspar, apatite, quartz and unstable biotite. Phonolites are peralkaline. Trachytes (peralkaline and non-peralkaline) and rhyolites are characterised by their sodic mineralogy with aegirine-augite, richterite, and arfvedsonite phenocrysts. There is a large compositional gap between basaltic and felsic lavas, except the mugearites. Despite this gap, major- and trace-element distributions are in favour of a co-magmatic origin for the basaltic and felsic lavas. The Upper Benue valley basalts are similar in their chemical and isotopic features to other basalts from both the continental and oceanic sectors of the Cameroon Line. The Upper Benue valley basaltic magmas (⁸⁷Sr/⁸⁶SrƸ.7035; k Nd=+3.9) originate from an infra-lithospheric reservoir. The Sr-Nd isotopic composition and high Sr contents of the mugearites suggest that they are related to mantle-derived magmas and that they result from the mixing, at shallow crustal levels, of a large fraction of trachytic magma with a minor amount of basaltic magma. Major-element modelling of the basalt-trachyte evolution (through hawaiite and mugearite compositions) does not support an evolution through fractional crystallization alone. The fluids have played a significant role in the felsic lavas genesis, as attested by the occurrence of F-rich minerals, calcite and analcite. An origin of the Upper Benue valley rhyolitic magmas by fractional crystallization of mantle-derived primitive magmas of basaltic composition, promoted or accompanied by volatile, halogen-rich fluid phases, may be the best hypothesis for the genesis of these lavas. These fluids also interact with the continental crust, resulting in the high Sr-isotope initial ratios (0.710) in the rhyolites, whereas the Nd isotopic composition has been less affected (k Nd=+0.4).     

Isotopic Heterogeneities in the Granitic Intrusion of Monte Capanne (Elba Island, Italy) and Dating Concepts

The Monte Capanne granodiorite-rhyolite-aplite association exhibitsK-Ar ages which cluster around 7.9 m.y. Rb-Sr mineral ages andU-Pb dating on zircons, however, give 6.2 m.y. which is thepreferred age of emplacement. Evidence of subsequent eventsrelated to either dyke emplacement, or conductive/convectivecooling is provided by ages as young as 5.4 m.y. A significantheterogeneity of the whole-rock ⁸⁷Sr/⁸⁶Sr initial ratios, whichfall in the range 0.711–0.715, is interpreted as beingdue in part to exchanges with the low ⁸⁷Sr⁸⁶Sr country rocksat the deuteric stage via fluid interaction, and in part topossible different magma sources. In the geological future,these heterogeneities should be progressively smeared out bythe radioactive decay of ⁸⁷Rb, but even if the system remainsperfectly closed, a residual bias in excess of 100 m.y. shouldpermanently affect the theoretical isochron ages. It is inferredthat Rb-Sr isochron ages determined on samples of Precambrianage must be regarded with caution: a residual bias may somewhatalter the information obtained even from statistically acceptableisochrons. In this respect, when great accuracy is needed forplutonic emplacement ages (to within few m.y.), U-Pb datingappears to be less sensitive to inherited components and providesmore reliable chronometric information.     

Intra-Grain Sr Isotope Evidence for Crystal Recycling and Multiple Magma Reservoirs in the Recent Activity of Stromboli Volcano, Southern Italy

Over the last several hundred years, Stromboli has been characterizedby steady-state Strombolian activity. The volcanic productsare dominated by degassed and highly porphyritic (HP-magma)black scoria bombs, lapilli and lava flows of basaltic shoshoniticcomposition. Periodically (about one to three events per year),more energetic explosive eruptions also eject light colouredvolatile-rich pumices with low phenocryst content (LP-magma)that have more mafic compositions than the HP-magma. An in situmajor and trace element and Sr isotope microanalysis study ispresented on four samples chosen to characterize the differentmodes of activity at Stromboli: a lava flow (1985–1986effusive event), a scoria bomb from the ‘normal’present-day activity of Stromboli (April 1984), and a scoriaand coeval pumice sample from a recent more explosive eruption(September 1996). Plagioclase (An_62–90) and clinopyroxene(Mg-number between 0·69 and 0·91) phenocrystsin all samples record marked major element variations. Largeand comparable Sr isotope variations have been detected in plagioclaseand clinopyroxene. HP-magma crystals have resorbed cores, witheither high ⁸⁷Sr/⁸⁶Sr (0·70635–0·70630)or low ⁸⁷Sr/⁸⁶Sr (0·70614–0·70608); thelatter values are similar to the values of the outer cores.Mineral rims and glassy groundmasses generally have intermediate⁸⁷Sr/⁸⁶Sr (0·70628–0·70613). Similarly,mineral growth zones with three groups of ⁸⁷Sr/⁸⁶Sr values characterizeminerals from the LP-pumice, with the lowest values presentin mineral rims and groundmass glass. These results define amixing process between HP- and LP-magmas, plus crystallizationof clinopyroxene, plagioclase and olivine, occurring in a shallowmagma reservoir that feeds the present-day magmatic activityof Stromboli. An important observation is the presence of athird component (high ⁸⁷Sr/⁸⁶Sr in mineral cores) consideredto represent a pre-AD 1900 cumulus crystal mush reservoir situatedjust below the shallow magma chamber. These cumulus phases areincorporated by the LP-magma arriving from depth and transportedinto the shallow reservoir. A rapid decrease of ⁸⁷Sr/⁸⁶Sr inthe replenishing LP-magma immediately prior to eruption of theAD 1985 lava flow is associated with an increased volume ofLP-magma in the shallow magma chamber. The HP-magma in the shallowreservoir is not fully degassed when it interacts with the LP-magma,making efficient mixing possible that ultimately produces awell overturned homogeneous magma. Further degassing and crystallizationoccur at shallower levels as the HP-magma moves through a conduitto the surface. KEY WORDS: isotopic microsampling; mineral recycling; mixing; Sr isotope disequilibria; Stromboli