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     

The Range of Spinel Compositions in Terrestrial Mafic and Ultramafic Rocks

Compositional fields for spinels from a wide variety of mafic–ultramaficigneous rock types and tectonic environments have been determinedfrom a global database of over 26 000 analyses. These fieldsare defined using contoured data density plots based on thespinel prism, and plots of T iO₂ vs ferric iron, for mantlexenoliths, ophiolitic rocks, continental layered intrusions,alkalic and lamprophyric rocks, tholeiitic basalts, Alaskanultramafic complexes and komatiites. Several trends appear regularlyin the various environments: a trend of widely variable Cr/(Cr+ Al) at low Fe²⁺/(Mg + Fe²⁺) (the Cr–Al trend); increasingFe³⁺, Fe²⁺/(Mg + Fe²⁺) and T iO₂ at constant Cr/(Cr + Al) (Fe–Ti trend); a trend found primarily in kimberlites, similar toFe–T i but at constant Fe²⁺/(Mg + Fe²⁺); and an unusualtrend of increasing Al found only in layered intrusions. TheCr–Al and Fe–T i trends are both found to varyingdegrees in tholeiitic basalts. The Cr–Al trend is prevalentin rocks that have equilibrated over a range of pressures, whereasthe Fe–T i trend is dominantly due to low-pressure fractionation.The most Cr-rich chromites found in nature occur in boninites,diamond-bearing kimberlites, some komatiites and ophioliticchromitites. Exceptionally reduced chromites are found in somekomatiites and in ophiolitic chromitites. Detrital chromitesfrom the Witwatersrand conglomerates are of komatiitic provenance. KEY WORDS: basalt; chromite; kimberlite; ophiolite; spinel     

A Transitional Basalt-Pantellerite Sequence of Fractional Crystallization, the Boina Centre (Afar Rift, Ethiopia)

Volcanological and petrological evidence, ⁸⁷Sr/⁸⁶Sr data, thelinear correlation between pairs of residual elements (e.g.Th, U, Zr, Hf, La, Ce, Ta) indicate that the rock series frommildly alkaline (transitional) basalt to pantellerite eruptedin recent Quaternary times at the Boina volcanic centre, canbe entirely explained in terms of fractional crystallizationat shallow depth. The fractionation process has been reconstructedby referrin to variation diagrams of major and trace elementsreported as a function of the fraction (f) of the initial compositionformed by the residual liquid, evaluated from the distributionof residual elements and by estimating the composition of theparent magma. The main crystal phases involved in the differentiationare, in the order of appearance: olivine, plagioclase, clinopyroxene,Fe-Ti oxides, alkali feldspar. Crystallization of Fe-Ti oxidesoccurs only at an advanced stage of fractionation in iron richliquids (ferrobasalts). The transition to the peralkaline field(near f=0?20) occurs without passing through a ‘true’trachytic (low-silica) salic stage and is determined by the‘plagioclase effect’. Fractionation within the peralkalinefield is dominated by alkali feldspar. Evidence is given fora ‘low-temperature zone’ of the oversaturated mildlyperalkaline system running along a line of constant alkali-ratio.Po₂ variations are recorded during the evolution of the Boinaseries as suggested by petrological data and distribution curvesof total iron, Fe⁺⁺/Fe⁺⁺⁺and europium. Po₂ values calculatedfrom europium distribution in feldspar and whole rocks agreewith published Po₂ mineralogical calculations in pantelleritesfrom other localities. A crucial stage is recognized near thetransition to the peralkaline field, with a sudden Po₂ dropduring the crystallization of the oxides probably provokingthe precipitation of apatite, followed by a rapid Po₂ increaseat f=0?30. This limited oxygen unbuffered zone is importantin the basalt-pantellerite evolution, as it determines markedchemical variations in a restricted crystallization interval.It is suggested that such a crucial stage occurs also in theother known pantellerite series, such as Pantelleria. It mayalso account for the scarcity of rocks frequently reported atthis stage (‘Daly gap’). Data obtained from Boina and comparisons with other volcanicseries indicate that many peralkaline rhyolites are geneticallyrelated to transitional basalts and that their nature is mainlycontrolled by the composition of the parent basaltic magma.The association is characteristically found in zones of extensionof both continental and oceanic environments. The views of Coombs(1963) are confirmed and the rocks series from transitionalbasalts to comendites and/or pantellerites should be distinguishedfrom the alkalic (undersaturated) igneous rock suites producedby differentiation of alkali basalts.     

A potassium-rich Alkalic Suite from the Deccan Traps,Rajpipla, India

The Rajpipla Alkalic Suite is the most potassium-enriched group of basaltic rocks so far described from the Deccan Traps. In the same area however early tholeiitic flows and late tholeiitic dykes show the potassium-poor nature characteristic of most Deccan Trap magmas. The rocks of the alkalic suite are highly porphyritic and their major element variation can be interpreted in terms of crystal fractionation dominated by clinopyroxene. Plagioclase, which is an important phenocryst phase, has fractionated only in relatively small amounts as a result of a lack of density contrast between it and the liquids. A dyke-like form for the magma chambers in which fractionation has taken place is postulated to account for the abundance of highly porphyritic types. The Rajpipla area is also notable as being one of the few Deccan localities where rhyolites are found.Abbreviations AB ankaramitic basalt - PB porphyritic basalt - PTB porphyritic trachybasalt - FPM feldsparphyric mugearite - M mugearite - TR trachyte - P. RHY potassic rhyolite - Th. B. tholeiitic basalt - Th. D. tholeiitic dolerite - Af alkali feldspar     

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     

Liquid Lines of Descent of Island Arc Magmas and Genesis of Rhyolites: Evidence from the Shirahama Group, Japan

The Mio-Pliocene Shirahama Group, Izu Peninsula, Central Japan,a well-exposed submarine volcanic arc complex of lava flows,pyroclastic rocks and associated shallow intrusives, is characterizedby a tholeiitic series (basalt to dacite) and a calc-alkalineseries (andesite to dacite). Chemical variations in the tholeiiticseries and calc-alkaline series are consistent with crystalfractionation from basalt and magnesian andesite (boninite),respectively. Crystal–liquid phase relations of thesemagmas have been investigated by study of sample suites fromthese two series. Compositions of liquids in equilibrium withphenocrysts were determined by microprobe grid analyses, inwhich 49 points were averaged in 03 mm 03 mm groundmassareas. The liquid compositions, coupled with the phenocrystmineralogy of the same samples, define the liquid lines of descentof these volcanic arc magmas. Major findings include the following:(1) Crystallization of the tholeiitic series magma is consistentwith early stage crystallization in the simple system Fo–Di–Silica–H₂O,with olivine having a reaction relation to augite and the tholeiiticliquid. (2) The later stage products of the tholeiitic seriesmagma are, however, crystal-poor (<10%) dacites with no maficminerals, suggesting that tholeiitic liquids, hypersthene andaugite were no longer on the cotectic (3) A characteristic ofthe calc-alkaline series magmas is the development of rhyoliticliquids. Hypersthene, augite, plagioclase and Fe–Ti oxideoccur in most calc-alkaline rocks studied, and hornblende andquartz can be found in about half of these. However, their differentiationpaths show that the cotectic relation between quartz and liquidended at a later stage, resulting in the resorption of quartzphenocrysts and ultimately in the formation of quartz-free magmas.(4) The late-stage liquids of both the tholeiitic and calc-alkalineseries have deviated from their cotectics, which cannot be explainedby fractional crystallization alone. The addition of H₂O froman outside system is probably required to explain the differentiationpaths. (5) The formation of chilled margins, the in situ crystallizationof a magma chamber in the solidification zone, and/or the migrationof groundwater into the magma chamber are thought to be likelyprocesses affecting magmas during their migration and intrusioninto the crust. An extreme effect of H₂O addition would be tolower the liquidus temperatures of all precipitating silicatephases far below their restorable range before eruption, resultingin the production of aphyric magmas. Even when a temperaturedecrease in the magma chamber causes a liquid to intersect theliquidus of a pre-existing phase, the addition of H₂O shiftsthe cotectic toward SiO₂, resulting in quartz being the lastphase to crystallize. The resorption of quartz is interpretedto be the result of a liquidus boundary shift caused by theaddition of H₂O. The genesis of aphyric rhyolites is thereforeinferred to result from fractional crystallization followingaddition of H₂0. KEY WORDS: Shirahama Group; Japan; island arc; rhyolite; magma series     

The Peralkaline Volcanic Suite of Aden and Little Aden, South Arabia

The volcanic rocks of Aden, Little Aden, and Ras Imran, heredesignated as belonging to the Aden Volcanic Series, were eruptedthrough central-vent, strato-volcanoes about 5 m.y. ago. Inits major element chemistry the Aden Volcanic Series is intermediatebetween the alkaline and tholeiitic associations, and this isdemonstrated by comparing it with the alkaline suite of Hawaiiand the tholeiitic series of Thingmuli, Iceland. It is proposedthat the most acceptable ‘parental’ magma is a mildlyalkaline olivine basalt which, on fractionation, produced aseries ranging from trachybasalts through trachyandesites andtrachytes to rhyolites. These rhyolites are peralkaline as themolecular proportion of alumina is less than that of the combinedalkalis, and are comenditic as the series is poor in normativefemic constituents. Trace element data suggest that the peralkalinesilicic eruptives are chemically comparable with those of MayorIsland, New Zealand, where a mildly alkaline olivine basaltparent has also been postulated. Although the age of eruption of c. 5 m.y., given by K-Ar measurements,is entirely consistent with an age deduced from geomorphologicalcriteria, an ⁸⁷Sr/⁸⁶Sr versus ⁸⁷Rb/⁸⁶Sr isochron plot suggeststhat the series is related to a thermal event some 20-30 m.y.older than the age of eruption. As this earlier age correspondsdirectly to the age of the previous magmatic episode, the eruptionof the Yemen Trap Series, the upper part of which is petrologicallysimilar to the Aden Volcanic Series, and as the initial ⁸⁷Sr/⁸⁶Srratios suggest that the magma originated in the mantle, it isproposed that the most acceptable petrogenetic scheme, whichwould also explain the anomalously old Rb-Sr age, is: (a) Partialfusion in the upper mantle giving rise to the alkaline YemenTrap Series, (b) After the cessation of surface activity, alarge body of magma existed in the upper mantle and this magma,on crystallizing, fractionated to produce a layered sequence,(c) About 5 m.y. ago some event, either pressure relief or furtherthermal activity, resulted in the partial remelting of thisfractionated plutonic sequence and the liquids so formed reachedthe surface without significant mixing or chemical fractionation.     

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.     

The Prinsen af Wales Bjerge Formation Lavas, East Greenland: the Transition from Tholeiitic to Alkalic Magmatism during Palaeogene Continental Break-up

We present elemental and isotopic (Sr–Nd–Pb–Hf–Os–He)data on primitive alkalic lavas from the Prinsen af Wales Bjerge,East Greenland. Stratigraphical, compositional and ⁴⁰Ar–³⁹Ardata indicate that this inland alkalic activity was contemporaneouswith the upper parts of the main tholeiitic plateau basaltsand also post-dated them. The alkalic rocks show a marked crustalinfluence, indicating establishment of new magmatic plumbingsystems distinct from the long-lived coastal systems that fedthe relatively uncontaminated plateau basalts. The least contaminatedlavas have high ³He/⁴He isotope ratios (R/R_A 12·4–18·5),sub-chondritic ¹⁸⁷Os/¹⁸⁸Os_i (0·120–0·126),low     

Experimental and Thermodynamic Constraints on the Sulphur Yield of Peralkaline and Metaluminous Silicic Flood Eruptions

Many basaltic flood provinces are characterized by the existenceof voluminous amounts of silicic magmas, yet the role of thesilicic component in sulphur emissions associated with trapactivity remains poorly known. We have performed experimentsand theoretical calculations to address this issue. The meltsulphur content and fluid/melt partitioning at saturation witheither sulphide or sulphate or both have been experimentallydetermined in three peralkaline rhyolites, which are a majorcomponent of some flood provinces. Experiments were performedat 150 MPa, 800–900°C, fO₂ in the range NNO –2 to NNO + 3 and under water-rich conditions. The sulphur contentis strongly dependent on the peralkalinity of the melt, in additionto fO₂, and reaches 1000 ppm at NNO + 1 in the most stronglyperalkaline composition at 800°C. At all values of fO₂,peralkaline melts can carry 5–20 times more sulphur thantheir metaluminous equivalents. Mildly peralkaline compositionsshow little variation in fluid/melt sulphur partitioning withchanging fO₂ (D_S 270). In the most peralkaline melt, D_S risessharply at fO₂ > NNO + 1 to values of >500. The partitioncoefficient increases steadily for S_bulk between 1 and 6 wt% but remains about constant for S_bulk between 0·5 and1 wt %. At bulk sulphur contents lower than 4 wt %, a temperatureincrease from 800 to 900°C decreases D_S by 10%. These results,along with (1) thermodynamic calculations on the behaviour ofsulphur during the crystallization of basalt and partial meltingof the crust and (2) recent experimental constraints on sulphursolubility in metaluminous rhyolites, show that basalt fractionationcan produce rhyolitic magmas having much more sulphur than rhyolitesderived from crustal anatexis. In particular, hot and dry metaluminoussilicic magmas produced by melting of dehydrated lower crustare virtually devoid of sulphur. In contrast, peralkaline rhyolitesformed by crystal fractionation of alkali basalt can concentrateup to 90% of the original sulphur content of the parental magmas,especially when the basalt is CO₂-rich. On this basis, we estimatethe amounts of sulphur potentially released to the atmosphereby the silicic component of flood eruptive sequences. The peralkalineEthiopian and Deccan rhyolites could have produced 10¹⁷ and10¹⁸ g of S, respectively, which are comparable amounts to publishedestimates for the basaltic activity of each province. In contrast,despite similar erupted volumes, the metaluminous Paraná–Etendekasilicic eruptives could have injected only 4·6 x 10¹⁵g of S in the atmosphere. Peralkaline flood sequences may thushave greater environmental effects than those of metaluminousaffinity, in agreement with evidence available from mass extinctionsand oceanic anoxic events. KEY WORDS: silicic flood eruptions; sulphur; experiment; Ethiopia; Deccan     

Palaeogene Continental to Oceanic Magmatism on the SE Greenland Continental Margin at 63{degrees}N: a Review of the Results of Ocean Drilling Program Legs 152 and 163

Drilling along a 63°N transect off SE Greenland during OceanDrilling Program (ODP) Legs 152 and 163 recovered a successionof volcanic rocks representing all stages in the break-up ofthe volcanic rifted margin. The rocks range from pre-break-upcontinental tholeiitic flood basalt, through syn-break-up picrite,to truly oceanic basalt forming the main part of the seaward-dippingreflector sequence (SDRS). All the lava flows recovered fromthe transect were erupted in a subaerial environment. ⁴⁰Ar–³⁹Ardating shows that the earliest magmas were erupted at     

Petrogenesis of Volcanic Rocks from Saipan and Rota, Mariana Islands, and Implications for the Evolution of Nascent Island Arcs

An ⁴⁰Ar/³⁹Ar age of 45·1 Ma determined for lavas fromnorthern Saipan confirms that these high-silica rhyolites eruptedduring the ‘proto-arc’ stage of volcanism in theIzu–Bonin–Mariana system, which is characterizedelsewhere by eruption of boninitic lavas. Incompatible traceelement concentrations and Sr, Hf, Nd, and Pb isotope ratiosfor these rhyolites are transitional between those of c. 48Ma boninitic lavas and post-38 Ma ‘first-arc’ andesitesand dacites from Saipan and Rota that have typical subduction-relatedcompositions. These transitional compositions are modeled bycrystal fractionation of parental tholeiitic basalt combinedwith assimilation of young boninitic crust. A second stage ofRayleigh fractionation in the upper crust is required by SiO₂concentrations that exceed 77 wt % and near-zero compatibleelement concentrations. First-arc magma compositions are consistentwith fractionation of basalt and assimilation of crust similarin composition to the first-arc magmas themselves. The mantlesources of the proto-arc and first-arc lavas from Saipan andRota are similar to those of Philippine back-arc basin basaltsbased on Nd and Hf isotopic compositions. The Pb isotope compositionsof these lavas are between those of Pacific sea-floor basaltsand Jurassic and younger cherty and clay-rich sediments. Thiscontrasts with the boninitic proto-arc volcanic rocks from Guamand Deep Sea Drilling Project Sites 458 and 459 that have Pbisotope compositions similar to Pacific basin basalts and volcaniclasticsediments. The preferred explanation for the difference in thenature of proto-arc volcanism between Saipan and other fore-arclocations is that the crust ceased extending 3–4 Myr earlierbeneath Saipan. This was caused by a change from mantle upwelling,fore-arc extension, and shallow melting to an environment dominatedby more normal mantle wedge convection, stable crust, and deepermelting. KEY WORDS: rhyolite; andesite; Mariana arc; isotope ratios; trace elements     

Petrogenesis of Dunite Xenoliths from Koolau Volcano, Oahu, Hawaii: Implications for Hawaiian Volcanism

Ultramafic xenoliths from Koolau Volcano on the island of Oahu,Hawaii, are divided into spinel lherzolite, pyroxenite, anddunite suites. On the basis of a study of the petrography andmineral compositions of 43 spinel lherzolites, 12 pyroxenites,and 20 dunites, the following characteristics of the dunitesin relation to the other nodule types and to Hawaiian lavasemerge. (1) The forstente content of olivines in the Koolaudunites (Fo_82.6-Fo_{89 7} ) overlap those of Hawaiian tholeiiticand alkalic lavas and are generally lower than those in abyssallherzolites and dunites and in Koolau spinel lherzolites. (2)Most of the dunites contain no orthopyroxene, all except twocontain chrome spinel, and a few contain interstitial plagioclaseand clinopyroxene. (3) Chrome spinels from the Koolau dunitesare distinctly higher in Cr/(Cr+Al), lower in Mg/(Mg+ Fe²⁺)and higher in TiO₂ than those from abyssal basalts and peridotites.Chrome spinels in the dunites correspond closely in compositionto chrome spinels in Hawaiian tholeiitic and alkalic lavas.(4) The abundance of dunite relative to other nodule types decreasesoutward from the central part of the volcano. The dunites areinterpreted not as residues of partial fusion of the mantlebut as crystal accumulations stored at shallow depths beneaththe central part of Koolau Volcano and derived from picriticmagmas parental to the shield-building tholeiitic lavas.     

Petrogenesis of Ultramafic Xenoliths from the 1800 Kaupulehu Flow, Hualalai Volcano, Hawaii

The 1800 Kaupulehu flow on Hualalai Volcano, Hawaii, containsabundant xcnoliths of dunitc, wehrlite, and olivine clinopyroxenitewith minor gabbro, troctolite, anorthosite, and wcbstcrite.The petrography and mineral compositions of 41 dunite, wehrlite,and olivine clinopyroxenite xenoliths have been studied, andclinopyroxene separates from eight of these have been analyzedfor Ba, K, Rb, Sr, rare earth elements, ⁸⁷Sr/⁸⁶Sr, and ¹⁴³Nd/¹⁴⁴Nd.Temperatures of equilibration obtained by olivine-spinel andpyroxene geothermometry range from 1000 to 1200 C. Mineralogicaldata combined with published fluid inclusion data indicate depthsof origin in the range of 8–30 km. The rarity of orthopyroxene, the presence of Fe-rich olivine(Fo⁸¹–⁸⁹) and clinopyroxene (Fs⁵–¹²), and the occurrenceof high TiO² in spinel (0.9–2.8 wt.%) and clinopyroxene(035–1.33 wt%) all indicate that the xenoliths are cumulates,not residues from partial fusion. The separated clinopyrox-eneshave ⁸⁷Sr/⁸⁶Sr (0-70348.0-70367) and ¹⁴³Nd/¹⁴⁴Nd (0.51293–0.51299)values that are different from Sr and Nd isotope ratios of Pacificabyssal basalts (>0.7032 and >0-5130, respectively). Also,clinopyroxenes and spinels in the xenoliths have generally higherTiO₂ contents (>O.35 and >0.91 wt.%, respectively) thantheir counterparts in abyssal cumulates (<0.40 and <0.70wt%,respectively). These differences indicate that the xenolithsare not a normal component of oceanic crust. Because the xenoliths and alkalic to transitional Hualalai lavashave similar values for Cr/(Cr + Al) and Cr/(Cr + Al + Fe³⁺)of spinels, ⁸⁷Sr/⁸⁶Sr of clinopyroxenes, and whole-rock ³He/⁴He,we conclude that the xenoliths are cumulates from such magmas.Multiple parental magmas for the xenoliths are indicated byslightly heterogeneous ⁸⁷Sr/⁸⁶Sr of clinopyroxene separates.Depths of formation of the xenoliths are estimated to be {smalltilde}8–30 km. Extensive crystallization of olivine in the absence of pyroxenesand plagioclase is a characteristic and prominent feature ofHawaiian tholeiitic magmatism. Dunite xenoliths crystallizedfrom alkalic magmas have previously been reported from MaunaKea Volcano (Atwill & Garcia, 1985) and Loihi Seamount (Clague,1988). Our finding of an alkalic signature for dunite xenolithsfrom a third Hawaiian volcano, Hualalai, shows that early olivinecrystallization should be considered a characteristic not justof Hawaiian tholeiitic magmatism but also of Hawaiian alkalicmagmatism.     

The 26{middle dot}5 ka Oruanui Eruption, Taupo Volcano, New Zealand: Development, Characteristics and Evacuation of a Large Rhyolitic Magma Body

The caldera-forming 26·5 ka Oruanui eruption (Taupo,New Zealand) erupted 530 km³ of magma, >99% rhyolitic, <1%mafic. The rhyolite varies from 71·8 to 76·7 wt% SiO₂ and 76 to 112 ppm Rb but is dominantly 74–76 wt% SiO₂. Average rhyolite compositions at each stratigraphiclevel do not change significantly through the eruption sequence.Oxide geothermometry, phase equilibria and volatile contentsimply magma storage at 830–760°C, and 100–200MPa. Most rhyolite compositional variations are explicable by28% crystal fractionation involving the phenocryst and accessoryphases (plagioclase, orthopyroxene, hornblende, quartz, magnetite,ilmenite, apatite and zircon). However, scatter in some elementconcentrations and ⁸⁷Sr/⁸⁶Sr ratios, and the presence of non-equilibriumcrystal compositions imply that mixing of liquids, phenocrystsand inherited crystals was also important in assembling thecompositional spectrum of rhyolite. Mafic compositions comprisea tholeiitic group (52·3–63·3 wt % SiO₂)formed by fractionation and crustal contamination of a contaminatedtholeiitic basalt, and a calc-alkaline group (56·7–60·5wt % SiO₂) formed by mixing of a primitive olivine–plagioclasebasalt with rhyolitic and tholeiitic mafic magmas. Both maficgroups are distinct from other Taupo Volcanic Zone eruptivesof comparable SiO₂ content. Development and destruction by eruptionof the Oruanui magma body occurred within 40 kyr and Oruanuicompositions have not been replicated in vigorous younger activity.The Oruanui rhyolite did not form in a single stage of evolutionfrom a more primitive forerunner but by rapid rejuvenation ofa longer-lived polygenetic, multi-age ‘stockpile’of silicic plutonic components in the Taupo magmatic system. KEY WORDS: Taupo Volcanic Zone; Taupo volcano; Oruanui eruption; rhyolite, zoned magma chamber; juvenile mafic compositions; eruption withdrawal systematics     

Geochemistry and Intrusive History of the Ashland Pluton, Klamath Mountains, California and Oregon

The Ashland pluton is a calc-alkaline plutonic complex thatintruded the western Paleozoic and Triassic belt of the KlamathMountains in late Middle Jurassic time. The pluton comprisesa series of compositionally distinct magma pulses. The oldestrocks are hornblende gabbro and two-pyroxene quartz gabbro withinitial ⁸⁷Sr/⁸⁶Sr = 0{dot}7044, ¹⁸O = 8{dot}7%, and REE patternswith chondrite normalized La/Lu = 7. These units were followedby a suite of tonalitic rocks (La_N/Lu_N = 7) and then by a suiteof K₂O- and P₂O₅ rocks of quartz monzodioritic affinity (La_N/Lu_N= 13–21; La_N/Sm_N = 2{dot}4–3{dot}) The quartz monzodioriticrocks were then intruded by biotite granodiorite and granitewith lower REE abundances but more fractionated LREE(La_N/Lu_N= 13–19; La_N/Sm_N = 4{dot}3–6 and they, in turn,were host to dikes and bosses of hornblende diorite. The latestintrusive activity consisted of aplitic and granitic dikes.Combined phase equilibria and mineral composition data, indicateemplacement conditions of approximately P_total = 2{dot}3kb,P_H2O between 1{dot}5 and 2{dot}2 kb, and f_O2 between the nickel-nickeloxide and hematite-magnetite buffers. Successive pulses of magma display increasing SiO₂ togetherwith increasing ¹⁸O and decreasing initial ⁸⁷Sr/⁸⁶Sr. The isotopicdata are consistent with either (1) combined fractional crystallizationof andesitic magma and concurrent assimilation of crustal materialcharacterized by low Sr₁ and high (¹⁸O or, more probably, (2)a series of partial melting events in which sources were successivelyless radiogenic but richer in ¹⁸O Each intrusive stage displaysevidence for some degree of crystal accumulation and/or fractionalcrystallization but neither process adequately accounts fortheir compositional differences. Consequently, each stage appearsto represent a distinct partial melting or assimilation event. The P₂O₅-rich nature of the quartz monzodiorite suite suggestsaccumulation of apatite. However, the suite contains abundantmafic microgranitoid enclaves and most apatite in the suiteis acicular. These observations suggest that magma mixing affectedthe compositional variation of the quartz monzodiorite suite.Mass balance calculations are consistent with a simple mixingprocess in which P₂O₅-rich alkalic basalt magma (representedby the mafic microgranitoid enclaves) was combined with a crystal-poorfelsic magma (represented by the tonalite suite), yielding aquartz monzodioritic magma that then underwent differentiationby crystal fractionation and accumulation.     

An Experimental Investigation of the Influence of Water and Oxygen Fugacity on Differentiation of MORB at 200 MPa

Crystallization experiments were performed at 200 MPa in thetemperature range 1150–950°C at oxygen fugacitiescorresponding to the quartz–fayalite–magnetite (QFM)and MnO–Mn₃O₄ buffers to assess the role of water andf_O2 on phase relations and differentiation trends in mid-oceanridge basalt (MORB) systems. Starting from a primitive (MgO9·8 wt %) and an evolved MORB (MgO 6·49 wt %),crystallization paths with four different water contents (0·35–4·7wt % H₂O) have been investigated. In primitive MORB, olivineis the liquidus phase followed by plagioclase + clinopyroxene.Amphibole is present only at water-saturated conditions below1000°C, but not all fluid-saturated runs contain amphibole.Magnetite and orthopyroxene are not stable at low f_O2 (QFM buffer).Residual liquids obtained at low f_O2 show a tholeiitic differentiationtrend. The crystallization of magnetite at high f_O2 (MnO–Mn₃O₄buffer) results in a decrease of melt FeO^*/MgO ratio, causinga calc-alkaline differentiation trend. Because the magnetitecrystallization temperature is nearly independent of the H₂Ocontent, in contrast to silicate minerals, the calc-alkalinedifferentiation trend is more pronounced at high water contents.Residual melts at 950°C in a primitive MORB system havecompositions approaching those of oceanic plagiogranites interms of SiO₂ and K₂O, but have Ca/Na ratios and FeO^* contentsthat are too high compared with the natural rocks, implyingthat fractionation processes are necessary to reach typicalcompositions of natural oceanic plagiogranites. KEY WORDS: differentiation; MORB; oxygen fugacity; water activity; oceanic plagiogranite     

Indian Continental Crust Recovered from Elan Bank, Kerguelen Plateau (ODP Leg 183, Site 1137)

At Site 1137 on Elan Bank of the Kerguelen Plateau, a largeigneous province in the southern Indian Ocean, a fluvial, volcaniclastic,polymict conglomerate and a fluvial sandstone are intercalatedwith subaerially erupted tholeiitic basalt flows. Clasts recoveredfrom the conglomerate have highly variable lithologies, includingalkali basalt, rhyolite, trachyte, granitoid and gneiss. Majorand trace element abundances and whole-rock isotopic data forthe sandstones, the conglomerate matrix and representative clastsfrom the conglomerate are used to infer the origin of thesediverse rock types. The gneiss clasts show an affinity to crustalrocks from India, particularly those of the Eastern Ghats Beltand its possible East Antarctic corollary, the Rayner Complex.The felsic volcanic clasts are not genetically related to theintercalated basalt flows, despite being erupted contemporaneouslywith these basaltic magmas. These felsic volcanic clasts probablyformed from partial melting of evolved upper continental crust.The granitoid also probably formed by partial melting of continentalcrust and could be an intrusive equivalent of the felsic volcanicrocks. In contrast, the alkali basalt clasts have isotopic compositionsthat are more similar to those of the tholeiitic basalt flowsrecovered at Site 1137; however, these clasts are highly alkalic(tephrite to phonotephrite) and have a distinct petrogenesisfrom the tholeiitic basalt flow units. KEY WORDS: geochemistry; Indian Ocean; Kerguelen Plateau; large igneous provinces; Ocean Drilling Program     

Crystallization of Chromite and Chromium Solubility in Basaltic Melts

The equilibrium between chromite and melt has been determinedon four basalts at temperatures of 1200–1400?C over arange of oxygen fugacity (f_o2) and pressures of 1 atm and 10kb. The Cr content of chromite-saturated melts at 1300?C and1 atm ranges from 0?05 wt.% Cr₂O₃ at a log f_o2= –3 to1?4 wt.% at a log f_o2=–12?8. The Cr²⁺/Cr³⁺ of melt increaseswith decreasing f_o2 and is estimated by assuming a constantpartitioning of Cr³⁺ between chromite and melt at constant temperature.The estimated values of Cr²⁺/Cr³⁺ in the melt are at f_o2 valuesof 4–5 orders of magnitude lower than the equivalent Fe²⁺/Fe³⁺values. The Cr/(Cr+Al) of chromite coexisting with melt at constanttemperature changes little with variation of f_o2 below log f_o2=–6.Five experiments at 10 kb indicate that Cr₂O₃ dissolved in themelt is slightly higher and the Cr/(Cr + Al) of coexisting chromiteis slightly lower than experiments at 1 atm pressure. Thus variationin total pressure cannot explain the large variations of Cr/(Cr+ Al) that are common to mid-ocean ridge basalt (MORB) chromite. Experiments on a MORB at 1 atm at f_o2 values close to fayalite-magnetite-quartz(FMQ) buffer showed that the Al₂O₃ content of melt is highlysensitive to the crystallization or melting of plagioclase,and consequently coexisting chromite shows a large change inCr/(Cr + Al). It would appear, therefore, that mixing of a MORBmagma containing plagioclase with a hotter MORB magma undersaturatedin plagioclase may give rise to the large range of Cr/(Cr +Al) observed in some MORB chromite.     

The Petrology of the Lower Old Red Sandstone Lavas of the Eastern Sidlaw Hills, Perthshire, Scotland

The calc-alkaline lava sequence of the eastern Sidlaw Hillsforms a small part of an extensive volcanic province of LowerOld Red Sandstone (Devonian) age in Scotland and N. England.The Sidlaw lavas ranging from olivine basalt to dacite are allporphyritic with combinations of olivine, plagioclase, clinopyroxene,orthopyroxene, and opaque oxide pheno-crysts. Chemically, thelavas are slightly more alkalic than modern calc-alkaline lavas.There is considerable variation in the ‘incompatible elements’.The differentiation of the lavas can be accounted for by fractionationof olivine+plagioclase+minor ore from a chemically variable,immediately parental magma at low pressure (c. 1 kb P_H2O). Itis suggested that fractionation of variable amounts of olivineand clinopyroxene from an olivine tholeiite at moderate P_H2Ocould give rise to this chemically variable, high alumina, immediatelyparental magma.