Plagioclase-free andesites from Zitácuaro (Michoacán), Mexico: petrology and experimental constraints

Approximately 150 km west of Mexico City in the central part of the Mexican Volcanic Belt (MVB) near Zitácuaro, Mexico, young volcanism has produced shield volcanoes, large volume silicic deposits, and fault-related basalt and andesite lava flows and cinder cones. This paper concerns a small cluster of Pleistocene andesite cones and flows which can be separated into two distinct groups: high-magnesium andesites (>6% MgO, 57–59% SiO₂), conveniently called basaltic andesites, with phenocrysts of orthopyroxene and augite, or augite and olivine; and andesites (60–62% SiO₂, <4.6% MgO), which have phenocrysts of orthopyroxene and augite, and ghosts of relict hornblende. Remarkably, plagioclase phenocrysts are absent, and evenly distributed but sparse (0.5–3.5%) quartz xenocrysts are present in all the lavas. In order to establish the conditions under which early crystallizing plagioclase is suppressed in these lavas, water saturated experiments up to 3 kbars were performed on one of the basaltic andesites. The conditions required to reproduce the phenocryst assemblages (either olivine + augite or opx + augite) are temperatures in excess of 1000 °C, with water saturated liquids (>3 wt%) at pressures of about 1 kbar. Compared to basaltic andesites of western Mexico, the Zitácuaro basaltic andesites have ∼2 wt% lower Al₂O₃ concentrations, which causes plagioclase to precipitate at significantly lower temperatures, and it therefore follows the crystallization sequence: olivine, augite, and orthopyroxene. Based on ubiquitous quartz xenocrysts, with glassy rhyolitic inclusions, a reasonable conclusion is that substantial mixing of a quartz-bearing rhyolitic magma with a parental basaltic andesite has occurred at low pressure (shallow depth), and this would account for the low Al₂O₃ concentrations in the Zitácuaro basaltic andesites. Whatever the mechanism of incorporation, the quartz xenocrysts are evidence of contamination of basaltic magma with more siliceous material, thus making it difficult to use these magmas as indicators of mantle melting processes. Received: 29 July 1997 / Accepted: 29 January 1998     

Crystallization Orders and Phase Chemistry of Glassy Lavas from the Pillow Sequences, Troodos Ophiolite, Cyprus

Three genetically unrelated magma suites are found in the extrusivesequences of the Troodos ophiolite, Cyprus. A stratigraphicallylower pillow lava suite contains andesite and dacite glassesand shows the crystallization order plagioclase; augite, orthopyroxene;titanomagnetite (with the pyroxenes appearing almost simultaneously).These lavas can in part be correlated chemically and mineralogicallywith the sheeted dikes and the upper part of the gabbro complexof the ophiolite. The second magma suite is represented in astratigraphically upper extrusive suite and contains basalticandesite and andesite glasses with the crystallizaton orderchromite; olivine; Ca-rich pyroxene; plagioclase. This magmasuite can be correlated chemically and mineralogically withparts of the ophiolitic ultramafic and mafic cumulate sequence,which has the crystallization order olivine; Ca-rich pyroxene;orthopyroxene; plagioclase. The third magma suite is representedby basaltic andesite lavas along the Arakapas fault zone andshows a boninitic crystallization order olivine; orthopyroxene;Ca-rich pyroxene; plagioclase. One-atmosphere, anhydrous phaseequilibria experiments on a lava from the second suite indicateplagioclase crystallization from 1225?C, pigeonite from 1200?C,and augite from 1165?C. These experimental data contrast withthe crystallization order suggested by the lavas and the associatedcumulates. The observed crystallization orders and the presenceof magmatic water in the fresh glasses of all suites are consistentwith evolution under relatively high partial water pressures.In particular, high P_H2O (1–3 kb) can explain the lateappearances of plagioclase and Ca-poor pyroxene in the majorityof the basaltic andesite lavas as the effects of suppressedcrystallization temperatures and shifting of cotectic relations.The detailed crystallization orders are probably controlledby relatively minor differences in the normative compositionsof the parental magmas. The basaltic andesite lavas are likelyto reach augite saturation before Ca-poor pyroxene saturation,whereas the Arakapas fault zone lavas, which have relativelyless normative diopside and more quartz, reached the Ca-poorpyroxene-olivine reaction surface and crystallized Ca-poor pyroxeneafter olivine.     

A petrological study of the younger Tongan andesites and dacites,and the olivine tholeiites of Niua Fo'ou Island,S. W. Pacific

Basaltic andesites are the dominant Tongan magma type, and are characterized by phenocrysts of augite, orthopyroxene (or rarely pigeonite), and calcic plagioclase (modally most abundant phase, and interpreted as the liquidus phase). The plagioclase phenocrysts exhibit slight oscillatory reverse zoning except for abrupt and thin more sodic rims, which are interpreted to develop during eruptive quenching. These rim compositions overlap those of the groundmass plagioclase. The pyroxene phenocrysts also exhibit only slight compositional zoning except for the outermost rim zones; the compositions of these rims, together with the groundmass pyroxenes, vary throughout the compositional range of subcalcic augite to ferroaugite through pigeonite to ferropigeonite, and are interpreted in terms of quench-controlled crystallization. This is supported, for example, by the random distribution of Al solid solution in the groundmass pyroxenes, compared to the more regular behaviour of Al in the phenocryst pyroxenes. The analysed Niua Fo'ou olivine tholeiites are aphyric; groundmass phases are plagioclase (An_17–88), olivine (Fa_18–63), titanomagnetite (usp. _59–73), and augite-ferroaugite which does not extend to subcalcic compositions; this is interpreted to be due to higher quenching temperatures and lower viscosities of these tholeiites compared to the basaltic andesites.Application of various geothermometers to the basaltic andesites suggest initial eruptive quenching temperatures of 1,008–1,124 ° C, plagioclase liquidus temperatures (1 bar) of 1,210–1,277 ° C, and orthopyroxene-clinopyroxene equilibration of 990–1,150 ° C. These calculated temperatures, together with supporting evidence (e.g. absence of olivine and amphibole, liquidus plagioclase, and plagioclase zoning patterns) are interpreted in terms of phenocryst crystallization from magmas that were either strongly water undersaturated, nearly anhydrous, or at best, water saturated at very low pressures (< 0.5 kb). This interpretation implies that these Tongan basaltic andesites did not originate by any of the currently proposed mechanisms involving hydrous melting within or above the Benioff zone.     

Trace element geochemistry of high alumina basalt - Andesite - Dacite - Rhyodacite lavas of the Main Volcanic Series of Santorini Volcano,Greece

Trace element systematics throughout the cal-calkaline high alumina basalt — basaltic andesite — andesite — dacite — rhyodacite lavas and dyke rocks of the Main Volcanic Series of Santorini volcano, Greece are consistent with the crystal fractionation of observed phenocryst phases from a parental basaltic magma as the dominant mechanism involved in generating the range of magmatic compositions. Marked inflection points in several variation trends correspond to changes in phenocryst mineralogy and divide the Main Series into two distinct crystallisation intervals — an early basalt to andesite stage characterised by calcic plagioclase+augite+olivine separation and a later andesite to rhyodacite stage generated by plagioclase augite+hypersthene+magnetite+apatite crystallisation. Percent solidification values derived from ratios of highly incompatible trace elements agree with previous values derived from major element data using addition-subtraction diagrams and indicate that basaltic andesites represent 47–69%; andesites 70–76%; dacites ca. 80% and rhyodacite ca. 84% crystallisation of the initial basalt magma. Least squares major element mixing calculations also confirm that crystal fractionation of the least fractionated basalts could generate derivative Main Series lavas, though the details of the least squares solutions differ significantly from those derived from highly incompatible element and addition-subtraction techniques. Main Series basalts may result from partial melting of the mantle asthenosphere wedge followed by limited olivine+pyroxene+Cr-spinel crystallisation on ascent through the sub-Aegean mantle and may fractionate to more evolved compositions at pressures close to the base of the Aegean crust. Residual andesitic to rhyodacite magmas may stagnate within the upper regions of the sialic Aegean crust and form relatively high level magma chambers beneath the southern volcanic centres of Santorini. The eruption of large volumes of basic lavas and silicic pyroclastics from Santorini may have a volcanological rather than petrological explanation.     

Plagioclase zonation styles in hornblende gabbro inclusions from Little Glass Mountain,Medicine Lake volcano,California: implications for fractionation mechanisms and the formation of composition gaps

The rhyolite of Little Glass Mountain (73–74% SiO₂) is a single eruptive unit that contains inclusions of quenched andesite liquid (54–61% SiO₂) and partially crystalline cumulate hornblende gabbro (53–55% SiO₂). Based on previous studies, the quenched andesite inclusions and host rhyolite lava are related to one another through fractional crystallization and represent an example of a fractionation-generated composition gap. The hornblende gabbros represent the cumulate residue associated with the rhyolite-producing and composition gap-forming fractionation event. This study combines textural (Nomarski Differential Interference Contrast, NDIC, imaging), major element (An content) and trace element (Mg, Fe, Sr, K, Ti, Ba) data on the style of zonation of plagioclase crystals from representative andesite and gabbro inclusions, to assess the physical environment in which the fractionation event and composition gap formation took place. The andesite inclusions (54–61% SiO₂) are sparsely phyric with phenocrysts of plagioclase, augite and Fe-oxide±olivine, +/–orthopyroxene, +/–hornblende set within a glassy to crystalline matrix. The gabbro cumulates (53–55% SiO₂) consist of an interconnected framework of plagioclase, augite, olivine, orthopyroxene, hornblende and Fe-oxide along with highly vesicular interstitial glass (70–74% SiO₂). The gabbros record a two-stage crystallization history of plagioclase+olivine+augite (Stage I) followed by plagioclase+orthopyroxene+ hornblende+Fe-oxide (Stage II). Texturally, the plagioclase crystals in the andesite inclusions are characterized by complex, fine-scale oscillatory zonation and abundant dissolution surfaces. Compositionally (An content) the crystals are essentially unzoned from core-to-rim. These features indicate growth within a dynamic (convecting?), reservoir of andesite magma. In contrast, the plagioclase crystals in the gabbros are texturally smooth and featureless with strong normal zonation from An₇₄ at the core to around An₃₀. K, and Ba abundances increase and Mg abundances decrease steadily towards the rim. Ti, Fe, and Sr abundances increase and then decrease towards the rim. The trace element variations are fully consistent with the two-stage crystallization sequence inferred from the gabbro mineralogy. These results indicate progressive closed-system in situ crystallization in a quiescent magmatic boundary layer environment located along the margins of the andesite magma body. The fractional crystallization that generated the host rhyolite lava is one of inward solidification of a crystallizing boundary layer followed by melt extraction and accumulation of highly evolved interstitial liquid. This mechanism explains the formation of the composition gap between parental andesite and rhyolite magma compositions.     

Mineralogy and proposed P-T paths of basaltic lavas from Rabaul caldera,Papua New Guinea

Rabaul caldera is a large volcanic depression at the north-east tip of New Britain, Papua New Guinea. The lavas range in composition from basalt to rhyolite and have a calc-alkalic affinity but also display features typical of tholeiites, including moderate absolute iron enrichment in flows cropping out around the caldera. The basalts contain phenocrysts of plagioclase and clinopyroxene with less abundant olivine and titanomagnetite. In the basaltic andesites olivine is rare, while orthopyroxene and titanomagnetite are common along with plagioclase and clinopyroxene. Orthopyroxene is also found mantling olivine in some of the basalts while in both rock types pigeonitic augite is a fairly common constituent of the groundmass. Plagioclase in both basalt and basaltic andesite often exhibits sieve texture and analysis of the glass blebs show them to be of similar composition to the bulk rock. Phenocrystic clinopyroxene is a diopsidic augite in both basalt and basaltic andesite. Al₂O₃ content of the clinopyroxene is moderately high (4%) and often shows considerable variation in any one grain. Calculations show that the microphenocrysts probably crystallised near the surface, while phenocrysts crystallised at around 7 kb (21 km). Neither the basalts nor the basaltic andesites would have been in equilibrium at any geologically reasonable P and T with quartz eclogite. Equilibration between mantle peridotite and a. typical Rabaul basaltic liquid could have occurred around 35 kb and 1270 °C. A basaltic andesite liquid yields a temperature of 1263 °C and a pressure of 28 kb for equilibration with mantle peridotite.Partial melting of sufficient volumes of mantle peridotite at these P's and T's requires about 15% H₂O, but there is no evidence that these magmas ever contained large amounts of water. It is proposed that the Rabaul magmas were initially generated by partial melting of subducted lithosphere and subsequently modified by minor partial melting as they passed through the overlying mantle peridotite.     

Crystal Accumulation and Magma Mixing in the Petrogenesis of Tholeiitic Andesites from Fukujin Seamount, Northern Mariana Island Arc

Fukujin Seamount is a large, active, submarine volcano on thevolcanic front in the northernseamount province (NSP) of theMariana island arc (MIA). Five dredge hauls from the summitand upper flanks of Fukujin recovered mainly highly porphyriticbasaltic andesites. A few nearly aphyric samples are medium-Ksiliceous andesites (SiO₂ = 62%, K₂O = 1•5%). Fukujin andmost other large arc-front volcanoes of the northern MIA havetholeiitic (iron-enrichment) fractionation trends. This contrastswith the calc-alkaline trends of many smaller seamounts. A negativecorrelation of modal plagioclase content with bulk-rock SiO₂,as well as bulk-rock major and trace element variation trends,and glass analyses, suggests that lavas with >30 vol.% phenocrystsand <55 wt.% SiO₂ are partial cumulates. The presence ofbimodal phenocryst populations along with reversed to normalzoning of phenocrysts is explained by magma mixing of andesiticand basaltic liquids. Hybrid basaltic andesites probably formedby the accumulation of plagioclase in a tholeiitic magma chamberundergoing replenishment and mixing at a shallow crustal level.A petrogenetic model is presented for the origin of basalticandesite by combined magma mixing and fractional crystallization.Aphyric siliceous andesites can be modelled by simple fractionationof basaltic andesite. The early fractionating assemblage consistedmainly of plagioclase and clinopyroxene, with lesser olivineand minor magnetite, but plagioclase remained suspended in themelt. The later fractionating assemblage was dominated by plagioclasewith orthopyroxene instead of olivine. ^*Present address: 2260 rue Panet, Montreal, Quebec, H2L 3A6, Canada.     

The evolution of young silicic lavas at Medicine Lake Volcano,California: Implications for the origin of compositional gaps in calc-alkaline series lavas

At Medicine Lake Volcano, California, the compositional gap between andesite (57–62 wt.% SiO₂) and rhyolite (73–74 wt.% SiO₂) has been generated by fractional crystallization. Assimilation of silicic crust has also occurred along with fractionation. Two varieties of inclusions found in Holocene rhyolite flows, hornblende gabbros and aphyric andesites, provide information on the crystallization path followed by lavas parental to the rhyolite. The hornblende gabbros are magmatic cumulate residues and their mineral assemblages are preserved evidence of the phases that crystallized from an andesitic precursor lava to generate the rhyolite lavas. The andesitic inclusions represent samples of a parental andesite and record the early part of the differentiation history. Olivine, plagioclase and augite crystallization begins the differentiation history, followed by the disappearance of olivine and augite through reaction with the liquid to form orthopyroxene and amphibole. Further crystallization of the assemblage plagioclase, amphibole, orthopyroxene, magnetite, and apatite from a high-SiO₂ andesite leads to rhyolite. This final crystallization process occurs on a cotectic that is nearly horizontal in temperature-composition space. Since a large amount of crystallization occurs over a limited temperature interval, a compositional gap develops between rhyolite and high SiO₂ andesite.Liquidus surfaces with shallow slopes in temperature-composition space are characteristic of several late-stage crystallization assemblages in the andesite to rhyolite compositional range. Experimentally produced plagioclase+ amphibole+orthopyroxene+magnetite and plagioclase+ augite+low-Ca pyroxene+magnetite cotectics have liquidus slopes that are nearly flat. At other calc-alkaline volcanic centers crystallization processes involving large compositional changes over small temperature intervals may also be important in the development of bimodal volcanism (i.e. the existence of a composition gap). At Mt. Mazama and Mt. St. Helens, USA and Aso Caldera and Shikotsu, Japan the amphibole-bearing assemblage was important. At Krakatau, Indonesia and Katmai, USA, an augite+orthopyroxene-bearing assemblage was important. In addition to its role in the production of a compositional gap between intermediate and rhyolitic lavas, the crystallization process increases the H₂O content of the residual liquid. This rapid increase in residual liquid volatile content which results from the precipitation of a large proportion of crystalline solids may be an important factor among several that lead to explosive silicic eruptions.     

The hydrous phase equilibria (to 3 kbar) of an andesite and basaltic andesite from western Mexico: constraints on water content and conditions of phenocryst growth

We have conducted high pressure (to 3 kbar), water saturated melting experiments on an andesite (62 wt% SiO₂) and a basaltic andesite (55 wt% SiO₂) from western Mexico. A close comparison between the experimental phase assemblages and their compositions, and the phenocryst assemblages of the lavas, is found in water saturated liquids, suggesting that the CO₂ content was minimal in the fluid phase. Thus the historic lavas from Volcan Colima (with phenocrysts of orthopyroxene, augite, plagioclase, and hornblende) were stored at a temperature between 950–975 °C, at a pressure between 700–1500 bars, and with a water content of 3.0–5.0 wt%. A hornblende andesite (spessartite) from Mascota, of nearly identical composition but with only amphibole phenocrysts, had a similar temperature but equilibrated at a minimum of 2000 bars pressure with a dissolved water content of at least 5.5 wt% in the liquid. Experiments on the basaltic andesite show that the most common natural phenocryst assemblages (olivine, ±augite, ±plagioclase) could have precipitated at temperatures from 1000–1150 °C, in liquids with a wide range of dissolved water content (∼2.0–6.0 wt%) and a corresponding pressure range. A lava of the same bulk composition with phenocrysts of hornblende, olivine, plagioclase, and augite is restricted to temperatures below 1000 °C and pressures below 2500 bars, corresponding to <5.5 wt% water in the residual liquid. Although there is some evidence for mixing in the andesites (sporadic olivine phenocrysts), the broad theme of the history of both lava types is that the phenocryst assemblages for both the andesitic magmas and basaltic andesitic magmas are generated from degassing and reequilibration on ascent of initially hydrous parents containing greater than 6 wt% water. Indeed andesitic magmas could be related to a basaltic andesite parent by hornblende-plagioclase fractionation under the same hydrous conditions. Received: 10 December 1996 / Accepted: 21 August 1997     

Petrology of Medicine Lake Highland volcanics: Characterization of endmembers of magma mixing

Lavas from Medicine Lake volcano, Northern California have been examined for evidence of magma mixing. Mixing of magmas has produced basaltic andesite, andesite, dacite and rhyolite lavas at the volcano. We are able to identify the compositional characteristics of the components that were mixed and to estimate the time lag between the mixing event and eruption of the mixed magma. Compositional data from pairs of phenocrysts identify a high alumina basalt (HAB) and a silicic rhyolite as endmembers of mixing. Mg-rich olivine or augite and Ca-rich plagioclase are associated with the HAB component, and Fe-rich orthopyroxene and Na-rich plagioclase are associated with the rhyolitic component. Some lavas contain multiple phenocryst assemblages suggesting the incorporation of several magmas intermediate between the HAB and silicic components. Glass inclusions trapped in Mg-rich olivine and Na-rich plagioclase are similar in composition to the proposed HAB and rhyolite end members and provide supportive evidence for mixing. Textural criteria are also consistent with magma mixing. Thermal curvature of the liquidus surfaces in the basalt-andesite-rhyolite system allows magmas produced by mixing to be either supercooled or superheated. Intergranular textures of basaltic andesites and andesites result from cooling initiated below the liquidus. The trachytic textures of silicic andesites form from cooling initiated above the liquidus. Reversed compositional zoning profiles in olivine crystals were produced by the mixing event, and the homogenization of the compositional zoning has been used to estimate the time interval between magma mixing and eruption. Time estimates are on the order of 80 to 90 h, suggesting that the mixing event triggered eruption.     

Hydrous Basaltic Andesites Associated with Minette and Related Lavas in Western Mexico

The convergent margin of western Mexico is uniquely characterizedby a volcanic front of lamprophyric and related lavas located{small tilde}70 km closer to the Middle America trench thanthe main axis of andesitic volcanism. This front, defined bysmall volcanic centers ranging in age from {small tilde}1 kato 3 Ma, contains several lava types: minette, absarokite, leucitite,spessartite, and kersantite, all without feldspar phenocrysts.Many of the lavas contain hydrous phenocrysts; they are enrichedin potassium and other incompatible elements, and they are moreoxidized relative to the andesitic suite of the main axis. Intimatelyassociated are flows of basaltic andesite of comparable volume.They range in composition from 53 to 58 wt.%SiO₂, have 5–9wt.%MgO and contain phenocrysts of olivine, sparse augite, andvarying amounts of plagioclase. Their alkali contents are typicalof calc-alkaline varieties, with average Na₂O and K₂O concentrationsof 4?2 and 1?1 wt.% respectively. The basaltic andesites oftencontain olivine of unusually high forsterite content, reflectingcrystallization under oxidizing conditions, and they have oxygenfugacities up to 3?3 log units above the Ni-NiO buffer. Manifestationsof high water contents are (1) the ubiquitous occurrence ofgroundmass olivine rather than orthopyroxene, and (2) the suppressionof plagioclase as an early crystallizing phase. Both featuresreflect the role of water in reducing the activity of silicain the melt. The progressive influence of water during crystallizationis also seen in the continuum between the two intermediate lavatypes, basaltic andesite and kersantite, as plagioclase is suppressedand hornblende is stabilized in the phenocryst assemblage. Thus,despite the absence of hydrous minerals in the basaltic andesites,their phenocryst assemblages reveal the influence of substantialamounts of water, and thereby show a genetic link to the variouslamprophyric lavas.     

Textural and compositional evidence for magma mixing and its mechanism,Abu volcano group,southwestern Japan

Quaternary basalts, andesites and dacites from the Abu monogenetic volcano group, SW Japan, (composed of more than 40 monogenetic volcanoes) show two distinct chemical trends especially on the FeO^*/MgO vs SiO₂ diagram. One trend is characterized by FeO^*/MgO-enrichment with a slight increase in SiO₂ content (Fe-type trend), whereas the other shows a marked SiO₂-enrichment with relatively constant FeO^*/MgO ratios (Si-type trend). The Fe-type trend is explained by fractional crystallization with subtraction of olivine and augite from a primitive alkali basalt magma. Rocks of the Si-type trend are characterized by partially melted or resorbed quartz and sodic plagioclase phenocrysts and/or fine-grained basaltic inclusions. They are most likely products of mixing of a primitive alkali basalt magma containing olivine phenocrysts with a dacite magma containing quartz, sodic plagioclase and hornblende phenocrysts. Petrographic variation as well as chemical variation from basalt to dacite of the Si-type trend is accounted for by various mixing ratios of basalt and dacite magmas. Pargasitic hornblende and clinopyroxene phenocrysts in andesite and dacite may have crystallized from basaltic magma during magma mixing. Olivine and spinel, and quartz, sodic plagioclase and common hornblende had crystallized in basaltic and dacitic magmas, respectively, before the mixing. Within a lava flow, the abundance of basaltic inclusions decreases from the area near the eruptive vent towards the perimeter of the flow, and the number of resorbed phenocrysts varies inversely, suggesting zonation in the magma chamber.The mode of mixing changes depending on the mixing ratio. In the mafic mixture, basalt and dacite magmas can mix in the liquid state (liquid-liquid mixing). In the silicic mixture, on the other hand, the basalt magma was quenched and formed inclusions (liquid-solid mixing). During mixing, the disaggregated basalt magma and the host dacite magma soon reached thermal equilibrium. Compositional homogenization of the mixed magma can occur only when the equilibrium temperature is sufficiently above the solidus of the basalt magma. The Si-type trend is chemically and petrographically similar to the calc-alkalic trend. Therefore, a calc-alkalic trend which is distinguished from a fractional crystallization trend (e.g. Fe-type trend) may be a product of magma mixing.     

Polybaric Evolution of Calc-alkaline Magmas from Nisyros, Southeastern Hellenic Arc, Greece

The lavas of Nisyros were erupted between about 0?2 m.y B.P.and 1422 A.D., and range in composition from basaltic andesiteto rhyodacite. Most were erupted prior to caldera collapse (exactdate unknown), and the post-caldera lavas are petrographically(presence of strongly resorbed phenocrysts) and chemically (lowerTiO₂ K₂O, P₂O₅, and LIL elements) distinct from the pre-calderalavas. The pre-caldera lavas do not form a continuous seriessince lavas with SiO₂ contents between 60 and 66 wt.% are absent.Nevertheless, major element variations demonstrate that fractionalcrystalliz ation (involving removal of olivine, dinopyroxene,plagioclase, and Fe-Ti oxide from the basaltic andesites andandesites and plagioclase, clinopyroxene, hypersthene, Ti-magnetite,ilmenite, apatite, and zircon from the dacites and rhyodacites)played a major role in the evolution of the pre-caldera lavas.Several lines of evidence indicate that other processes werealso important in magma evolution: (1) Quantitative modelingof major element data shows that phenocryst phases of unlikelycomposi tion or unrealistic assemblages of phenocryst phasesare required to relate the dacites and rhyodacites to the basalticandesites and andesites; (2) The proportions of olivine andclinopyroxene required in quantitative models for the initialstages of evolution differ from those observed petrographicallyand this is not likely to reflect either differential ratesof crystal settling or the curvature of cotectics along whichliquids of basaltic andesite to andesite composition lie; (3)The concentrations of Rb, Cs, Ba, La, Sm, Eu, and Th in therhyod.acites are too high for these lavas to be related to thedacites by fractional crystallization alone; and (4) ⁸⁷Sr/⁸⁶Srratios for the andesites and rhyodacites are higher than thosefor the basaltic andesites and dacites, respectively. It isshown that fractional crystallization was accompanied by assimilation,and that magma mixing played a minor role (if any) in the evolutionof the pre-caldera lavas. Trace element and isotopic data indicatethat the andesites evolved from the basaltic andesites by AFCinvolving average crust or upper crust, whereas the rhyodacitesevolved from the dacites by AFC involving lower crust. Additionalevidence for polybaric evolution is provided by the occurrenceof distinct Ab-rich cores of plagioclase phenocrysts in thedacites and rhyodacites, which record a period of high pressurecrystallization, and by the occurrence of both normal and reverse-zonedphenocrysts in the basaltic andesites and andesites. Furthermore,calculated pressures of crystallization are {small tilde}8 kbfor the dacites and rhyodacites and 3?5–4 kb for the basalticandesites and andesites. It is concluded that the dacites andrhyodacites evolved via AFC from basaltic andesites and andesiteslargely in chambers sited near the base of the crust whereasthe basaltic andesites and andesites mostly evolved in chamberssited at mid-crustal levels. Eruption from different chambersexplains the compositional gap in the chemistry of the pre-calderalavas since eruptive products represent a more or less randomsampling of residual liquids which separate (via filter pressing)from bodies of crystallizing magma at various depths. Magmamixing was important in the evolution of the post-caldera lavas,but geochemical data require that these magmas evolved fromparental magmas which were derived from a more refractory sourcethan the parental magmas to the pre-caldera lavas. ^*Present address: Netherlands Energy Research Foundation (ECN), P.O. Box 1, 1755 ZG Petten, The Netherlands     

Calc-alkaline, Shoshonitic, and Primitive Tholeiitic Lavas from Monogenetic Volcanoes near Crater Lake, Oregon

Quaternary monogenetic volcanism in the High Cascades of Oregonis manifested by cinder cones, lava fields, and small shields.Near Crater Lake caldera, monogenetic lava compositions include:low-K (as low as 0?09% K₂O) high-alumina olivine tholeiite (HAOT);medium-K. calc-alkaline basalt, basaltic andesite, and andesite;and shoshonitic basaltic andesite (2?1% K₂O, 1750 ppm Sr at54% SiO₂). Tholeiites have MORB-like trace element abundancesexcept for elevated Sr, Ba, and Th and low high field strengthelements (HFSE), and they represent near-primary liquids. Theyare similar to HAOTs from the Cascades and adjacent Basin andRange, and to many primitive basalts from intraoceanic arcs.Calc-alkaline lavas show a well-developed arc signature of highlarge-ion lithophile elements (LILE) and low HFSE. Their Zrand Hf concentrations are at least partly decoupled from thoseof Nb and Ta; HREE are low relative to HAOT. Incompatible elementabundances and ratios vary widely among basaltic andesites.Some calc-alkaline lavas vented near Mount Mazama contain abundantgabbroic microxcnoliths, and are basaltic andesitic magmas contaminatedwith olivine gabbro. A calc-alkaline basalt and a few basaltic andesites have MgOand compatible trace element contents that suggest only minorfractionation. There appears to be a compositional continuumbetween primitive tholeiitic and calc-alkaline lavas. Compositionalvariation within suites of comagmatic primitive lavas, boththoleiitic and calc-alkaline, mainly results from differentdegrees of partial melting. Sources of calc-alkaline primarymagmas were enriched in LILE and LREE by a subduction componentand contained residual garnet, whereas sources of HAOTs hadlower LILE and LREE concentrations and contained residual clinopyroxene.High and variable LILE and LREE contents of calc-alkaline lavasreflect variations in fluid-transported subduction componentadded to the mantle wedge, degree of partial melting, and possiblyalso interaction with rocks or partial melts in the lower crust. Andesites were derived from calc-alkaline basaltic andesitesby fractionation of plagioclase+augite+magnetite+apatite ? orthopyroxeneor olivine, commonly accompanied by assimilation. Many andesitesare mixtures of andesitic or dacitic magma and a basaltic orbasaltic andesitic component, or are contaminated with gabbroicmaterial. Mingled basalt, andesite, and dacite of Williams Craterformed by multi-component, multi-stage mixing of basaltic andesiticmagma, gabbro, and dacitic magma. The wide range of compositionsvented from monogenetic volcanoes near Crater Lake is a resultof the thick crust coupled with mild tectonic extension superimposedon a subduction-related magmatic arc.     

Temporal magmatic variation at Boqueron volcano,El Salvador

The relative ages of 21 lavas from Boqueron volcano in El Salvador were determined by superposition. The lavas are grey to black, porphyritic basalts, basaltic andesites and andesites with phenocrysts of plagioclase, augite, olivine, and magnetite. The andesitic lavas appear to have evolved from basaltic magma by fractionation of the observed phenocryst phases.The temporal variation in the chemical composition of the lavas at Boqueron is composed of three components. First, there is a crudely cyclical alternation of basalts and andesites. Second, these cycles are progressively shifted toward higher SiO₂ contents. Third, approximately in the middle of the stratigraphic section sampled, there is an abrupt change in chemical variation trends from an Al-rich and Fe-poor trend to an Fe-rich and Al-poor trend. This change is interpreted to have been caused by an increased proportion of plagioclase fractionation and a decreased porportion of augite fractionation. The crudely cyclical change in SiO₂ content with time is interpreted as a combination of crystal fractionation that increases SiO₂ content, followed by influxes of basaltic magma that mix with residual magma to decrease SiO₂ content. Successive cycles are shifted toward higher SiO₂ content because there is a significant volume of fractionated magma remaining in the chamber before each influx of basalt.     

The 1996 Eruption of Karymsky Volcano, Kamchatka: Historical Record of Basaltic Replenishment of an Andesite Reservoir

The simultaneous eruption in 1996 of andesite from Karymskyvolcano and of basalt from the Academy Nauk vent 6 km away appearsto provide a case of mafic recharge of an andesite reservoirfor which the time of recharge is exactly known and direct samplesof the recharging magma are available. The explosive phreato-magmaticeruption of basalt was terminated in less than 24 h, whereasandesite erupted continuously during the following 4 years.Detailed petrological study of volcanic ash, bombs and lavasof Karymsky andesite erupted during the period 1996–1999provides evidence for basaltic replenishment at the beginningof the eruptive cycle, as well as a record of compositionalvariations within the Karymsky magma reservoir induced by basalticrecharge. Shortly after the beginning of the eruption the compositionof the matrix glass of the Karymsky tephra became more maficand then, within 2 months, gradually returned to its originalstate and remained almost constant for the following 3 years.Further evidence for basaltic replenishment is provided by thepresence of xenocrysts of basaltic origin in the andesite ofKarymsky. A conspicuous portion of the plagioclase phenocrystsin the Karymsky andesite has calcic cores, with compositionsand textures resembling those of plagioclases in the AcademyNauk basalt. Similarly, the earlier portion of the andesiteof the eruption sequence contains rare olivines, which occuras resorbed cores in pyroxenes. The composition of the olivinematches that of olivines in the Academy Nauk basalt. The sequenceof events appears to be: (1) injection of basaltic magma intothe Karymsky chamber with immediate, compensating expulsionof pre-existing chamber magma from the Karymsky central vent;(2) direct mixing of basaltic and andesitic magmas with dispersalof phenocrysts associated with the basalt throughout the andesiteso that newly mixed magma appeared at the vent within 2 months;(3) re-establishment of thermal and chemical equilibrium withinthe reservoir involving crystallization in the new hybrid liquid,which returned the melt composition to ‘normal’,formed rims on inherited calcic plagioclase, and caused theresorption of dispersed olivine xenocrysts. Taken together,these findings indicate that the Karymsky magma reservoir wasrecharged by basalt at the onset of the 1996 eruptive cycle.The rapidity and thoroughness of mixing of the basalt with thepre-existing andesite probably reflects the modest contrastin temperature, viscosity, and density between the two magmas. KEY WORDS: Karymsky; Kamchatka; magma mixing; andesite; volcanic glass; plagioclase     

A detailed Th,Sr and O isotope study of Hekla: differentiation processes in an Icelandic Volcano

²³⁸U–²³⁰Th disequilibria and Sr and O isotope ratios have been measured in a suite of samples from most of the known prehistoric and historic eruptions of Hekla volcano, Iceland. They cover the compositional range from basaltic andesite to rhyolite. Recent basalts erupted in the vicinity of the volcano and a few Pleistocene basalts have also been studied. Geochemical data indicate that the best tracers of magmatic processes in Hekla are the (²³⁰Th/²³²Th) and Th/U ratios. Whereas most geochemical parameters, including Sr, Nd and O isotopes, could be compatible with crystal fractionation, (²³⁰Th/²³²Th) and Th/U ratios differ in the basalts and basaltic andesites (1.05 and 3.2, respectively) and in the silicic rocks, dacites and rhyolites (0.98 and 3.4–3.7, respectively). This observation precludes fractional crystallization as the main differentiation process in Hekla. On the basis of these results, the following model is proposed: basaltic magmas rise in the Icelandic crust and cause partial melting of metabasic rocks, leading to the formation of a dacitic melt. The basaltic magma itself evolves by crystal fractionation and produces a basaltic andesite magma. The latter can mix with the dacitic liquid to form andesites. At higher levels in the magma chamber, the dacitic melt sometimes undergoes further differentiation by crystal fractionation and produces subordinate volumes of rhyolites. Together all these processes lead to a zoned magma chamber. However, complete zoning is achieved only when the repose time between eruptions is long enough to allow the production of significant volumes of dacitic magma by crustal melting. This situation corresponds to the large plinian eruptions. Between these eruptions, the so-called intra-cyclic activity is characterized by the eruption of andesites and basaltic andesites, with little crustal melting. The magmatic system beneath Hekla most probably was established during the Holocene. The shape and the size of the magma chamber may be inferred from the relationships between the composition of the lavas and the location of the eruption sites. In a cross-section perpendicular to Hekla's ridge, a bell-shaped reservoir 5 km wide and 7 km deep appears the most likely; its top could be at depth of 8 km according to geophysical data.     

Magnesian andesite and basalt from Shodo-Shima Island,southwest Japan,and their bearing on the genesis of calc-alkaline andesites

Calc-alkaline andesites and olivine tholeiitic basalts are widely distributed on Shodo-Shima island, southwest Japan. The Fo content of olivine phenocrysts in the andesite is higher than in the basalt. The primary magma of the andesite, estimated on the basis of the olivine fractional crystallization model, is not basaltic but andesitic. The basalt contains both chromite and titanomagnetite as inclusions in olivine phenocrysts, while only chromite appears in the andesite. The Cr content of chromite in the andesite is higher than in the basalt. These facts again indicate that the andesite cannot be a fractionation product of the basalt, and that andesitic and basaltic primary magmas were generated independently.     

Experimental study into the petrogenesis of crystal-rich basaltic to andesitic magmas at Arenal volcano

Arenal volcano is nearly unique among arc volcanoes with its 42 year long (1968–2010) continuous, small-scale activity erupting compositionally monotonous basaltic andesites that also dominate the entire, ~7000 year long, eruptive history. Only mineral zoning records reveal that basaltic andesites are the result of complex, open-system processes deriving minerals from a variety of crystallization environments and including the episodic injections of basalt. The condition of the mafic input as well as the generation of crystal-rich basaltic andesites of the recent, 1968–2010, and earlier eruptions were addressed by an experimental study at 200 MPa, 900–1,050 °C, oxidizing and fluid-saturated conditions with various fluid compositions [H₂O/(H₂O + CO₂) = 0.3–1]. Phase equilibria were determined using a phenocryst-poor (~3 vol%) Arenal-like basalt (50.5?wt% SiO₂) from a nearby scoria cone containing olivine (Fo₉₂), plagioclase (An₈₆), clinopyroxene (Mg# = 82) and magnetite (X_ulvö = 0.13). Experimental melts generally reproduce observed compositional trends among Arenal samples. Small differences between experimental melts and natural rocks can be explained by open-system processes. At low pressure (200 MPa), the mineral assemblage as well as the mineral compositions of the natural basalt were reproduced at 1,000 °C and high water activity. The residual melt at these conditions is basaltic andesitic (55 wt% SiO₂) with 5 wt% H₂O. The evolution to more evolved magmas observed at Arenal occurred under fluid-saturated conditions but variable fluid compositions. At 1,000 °C and 200 MPa, a decrease of water content by approximately 1 wt% induces significant changes of the mineral assemblage from olivine + clinopyroxene + plagioclase (5 wt% H₂O in the melt) to clinopyroxene + plagioclase + orthopyroxene (4 wt% H₂O in the melt). Both assemblages are observed in crystal-rich basalt (15 vol%) and basaltic andesites. Experimental data indicate that the lack of orthopyroxene and the presence of amphibole, also observed in basaltic andesitic tephra units, is due to crystallization at nearly water-saturated conditions and temperatures lower than 950 °C. The enigmatic two compositional groups previously known as low- and high-Al₂O₃ samples at Arenal volcano may be explained by low- and high-pressure crystallization, respectively. Using high-Al as signal of deeper crystallization, first magmas of the 1968–2010 eruption evolved deep in the crust and ascent was relatively fast leaving little time for significant compositional overprint by shallower level crystallization.     

Fluorine geochemistry of quaternary volcanic rocks from Southwestern British Columbia: Some petrogenetic implications

Fluorine contents in 38 Quaternary volcanic rocks, representing calc-alkaline andesite eruptive groups from the Garibaldi Lake area, were determined by a selective ion-electrode method. A close relationship is evident between F abundance and the type of ferromagnesian phenocrysts present in the andesitic rocks. Hypersthene andesites have the lowest F contents (142–212 ppm), whereas hornblende-biotite andesites exhibit the highest F values (279–368 ppm); hornblende andesites have intermediate F contents (238–292 ppm). The hornblende-free Desolation Valley basaltic andesite has a lower F content than the hornblende-bearing Sphinx Moraine basaltic andesite (122 ppm versus 317–333 ppm).Different eruptive suites can be grouped on the basis of F differentiation patterns into (1) a hornblende-free lava series in which the F content of basaltic andesite is less than that of andesite, and (2) a hornblende-bearing lava series in which F contents remain constant or decrease slightly from basaltic andesite through dacite. Fluorine variation in the former series was controlled largely by fractionation of anhydrous minerals, whereas that in the latter was influenced by crystallization of amphibole, biotite and apatite.The distinctive F variation patterns of the two lava series appear to represent real differences in the volatile contents of Garibaldi Lake magmas. These different volatile concentrations may reflect varying degrees of magma-wallrock interaction, differences in the initial volatile contents of the primary magmas, or some combination of these factors.