Hydrogen content in clinopyroxene phenocrysts from Salina mafic lavas (Aeolian arc,Italy)

Clinopyroxene phenocrysts from the mafic calc-alkaline lavas of Salina (Aeolian arc, southern Tyrrhenian Sea, Italy) have been analysed to determine the hydrogen content and iron oxidation state of this early crystallized phase. The volcanic activity of Salina, starting at 168 ka and developed in several centres up to 24 ka, was dominated by calc-alkaline and high-K calc-alkaline basalts and andesites, with minor dacites and rhyolites. The presence of OH vibrational bands was detected in the IR spectra of clinopyroxenes phenocrysts from Corvo, Rivi-Capo (168–87 ka), Fossa delle Felci (108–59 ka) and Monte dei Porri (57 ka) eruptions. Corvo-Rivi-Capo basalts have clinopyroxenes with the lowest water contents 75–97 ppm H₂O by weight, whereas an increase in the hydrogen contents of clinopyroxenes from Fossa delle Felci centre, with 171–286 ppm H₂O by weight, and Monte dei Porri with 343–390 ppm H₂O by weight, was observed. Mössbauer spectroscopy showed only a limited variation on the Fe³⁺/Fe_tot ratio of the studied samples, and a very similar atomic Fe³⁺ content (0.042–0.047 a.p.f.u.) suggesting that only minor variation on fO₂ occurred during the crystallization of these clinopyroxenes. The water content of parental melts, calculated by applying an ^IVAl-dependent partition coefficient to the measured hydrogen contents of clinopyroxenes, is 0.4–0.8 wt% of water in melt for the Rivi-Capo-Corvo basalts, 0.5–3.7 wt% water in melt for Fossa delle Felci lavas and 1.6–2.6 wt% of water in melt for Monte dei Porri lavas. An increase in the maximum hydrogen contents of clinopyroxenes can be recognized during the evolution of the Salina volcano, with the highest hydrogen content measured in clinopyroxenes from Monte dei Porri where the eruptions were characterized by a high degree of explosivity, suggesting a key role of volatiles.     

长白山天池火山近代喷发中气象站组熔岩—碎屑岩流研究

中晚全新世以来,长白山天池火山的活动多为爆炸性喷发和形成火山碎屑流,熔岩流出较少,气象站组熔岩—碎屑岩流则是为数不多的熔岩溢流活动之一,它是天池火山一个寄生火山的喷发产物。气象站组熔岩—碎屑岩流的岩性为碱流岩质,岩浆粘度大,流动缓慢。据研究其喷发时间大约4 ka BP,应属天池火山的近代喷发产物。     

Petrological and experimental evidence for differentiation of water-rich magmas beneath St. Kitts,Lesser Antilles

St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An_≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An₉₇ and An₉₅, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH₂O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO₂ = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt Kd_Ca–Na and dissolved H₂O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H₂O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.     

Recycled oceanic crust in the Hawaiian Plume: evidence from temporal geochemical variations within the Koolau Shield

The subaerial surface of Koolau volcano is composed of lavas that define the distinctive endmember composition for Hawaiian shield lavas, known as the Koolau component, now designated as the Makapuu-stage. The geochemical characteristics of lavas recovered by the Koolau Scientific Drilling Project (KSDP) show that this distinctive composition forms a <300-m thick veneer. Below this veneer, from ~300m to 470 m below sea level, Koolau shield lavas transition to a composition similar to Mauna Loa lavas, now designated as the Kalihi-stage. This transition was gradual, occurring over >80 ka; therefore it was not caused by an abrupt event, such as a landslide. Among all Koolau shield lavas, there are correlations between radiogenic isotopic ratios of Sr, Nd and Pb and compositional characteristics, such as SiO₂ content (adjusted to be in equilibrium with Fo₉₀ olivine), Sr/Nb, La/Nb and Th/La. These long-term compositional and isotopic trends show that as the shield aged, there was an increasing role for an ancient recycled marine sediment component (<3% of the source) accompanied by up to 20% SiO₂-rich dacitic melt. This melt was generated by partial melting of garnet pyroxenite, probably kilometers in size, that formed from recycled basaltic oceanic crust. In detail, time series analyses of depth profiles of Al₂O₃/CaO, Sr/Nb, La/Nb and Th/La in the KSDP drill core show correlations among these ratios indicating that recycled oceanic crust contributed episodically, ~29 ka period, to the magma source during the prolonged transition from Kalihi- to Makapuu-stage lava compositions. The long-term geochemical trends show that recycled oceanic crust was increasingly important as the Koolau shield moved away from the plume and encountered lower temperature.     

The generation of a diverse suite of Late Pleistocene and Holocene basalt through dacite lavas from the northern Cascade arc at Mount Baker,Washington

Mt. Baker is a dominantly andesitic stratovolcano in the northern Cascade arc. In this study, we show that the andesites are not all derived from similar sources, and that open-system processes were dominant during their petrogenesis. To this end, we discuss petrographic observations, mineral chemistry, and whole rock major and trace element chemistry for three of Mt. Baker’s late Pleistocene to Holocene lava flow units. These include the basalt and basaltic andesite of Sulphur Creek (SC) (51.4–55.8 wt% SiO₂, Mg# 57–58), the Mg-rich andesite of Glacier Creek (GC) (58.3–58.7 wt% SiO₂, Mg# 63–64), and the andesite and dacite of Boulder Glacier (BG) (60.2–64.2 wt% SiO₂, Mg# 50–57). Phenocryst populations in all units display varying degrees of reaction and disequilibrium textures along with complicated zoning patterns indicative of open-system processes. All lavas are medium-K and calc-alkaline, but each unit displays distinctive trace element and REE characteristics that do not correlate with the average SiO₂ content of the unit. The mafic lavas of SC have relatively elevated REE abundances with the lowest (La/Yb)_N (~4.5). The intermediate GC andesites (Mg- and Ni-rich) have the lowest REE abundances and the highest (La/Yb)_N (~6.7) with strongly depleted HREE. The more felsic BG lavas have intermediate REE abundances and (La/Yb)_N (~6.4). The high-Mg character of the GC andesites can be explained by addition of 4% of a xenocrystic olivine component. However, their depleted REE patterns are similar to other high-Mg andesites reported from Mt. Baker and require a distinct mantle source. The two dominantly andesitic units (GC and BG) are different enough from each other that they could not have been derived from the same parent basalt. Nor could either of them have been derived from the SC basalt by crystal fractionation processes. Crystal fractionation also cannot explain the compositional diversity within each unit. Compositional diversity within the SC unit (basalt to basaltic andesite) can, however, be successfully modeled by mixing of basalt with compositions similar to the dacites in the BG unit. Given that the BG dacites erupted at ~80–90 ka, and a similar composition was mixed with the SC lavas at 9.8 ka, the process that produced this felsic end-member must have been repeatedly active for at least 70 ka.     

Mineral chemistry of lava flows from Linga area of the Eastern Deccan Volcanic Province,India

Several basaltic lava flows have been identified in the study area in and around Linga, in the Eastern Deccan Volcanic Province (EDVP) on the basis of distinctly developed structural zones defined by primary volcanic structures such as columnar joints and vesicles. These basaltic lava flows are spatially distributed in four different sectors, viz., (i) Bargona–Gadarwara (BG) sector (ii) Shikarpur–Linga (SL) sector (iii) Arjunvari–Survir Hill (AS) sector and (iv) Kukrachiman–Morand Hill (KM) sector. A three-tier classification scheme has been adopted for the characterization and classification of individual lava flows. Each lava flow consists of a Lower Colonnade Zone (LCZ) overlain by the Entablature Zone (EZ) and Upper Colonnade Zone (UCZ). The LCZ and UCZ grade into a distinct/indistinct Lower Vesicular Zone (LVZ) and Upper Vesicular Zone (UVZ), respectively. The LCZ and UCZ of the flows are characterized by columnar joints while the EZ is marked by multi-directional hackly jointing. The geometry of different joint patterns corresponds to different styles of cooling during solidification of lava flows. Detailed petrographic studies of the investigated lava flows reveal inequigranular phenocrystal basalts characterized by development of phenocrystal phases including plagioclase, clinopyroxene and olivine, whereas groundmass composition is marked by tiny plagioclase, clinopyroxene, opaque mineral and glass. Electron microprobe analyses indicate that the olivine has a wide range ∼Fo₂₂ to Fo₆₆ revealing a wide spectrum of compositional variation. Pyroxene compositions are distinctly designated as Quad pyroxenes. Phenocrystal pyroxenes are mostly diopsidic, while the groundmass pyroxenes mainly correspond to augite with a minor pigeonite component. Pyroxene phenocrysts are characterized by a prominent Ti-enrichment. Phenocrystal plagioclase grains are calcic (An_52.7–An_72.9), whereas groundmass plagioclase are relatively sodic (An_39.2–An_61.6). Groundmass opaque minerals are characteristically found to be Ti–magnetite/ilmenite/pyrophanite. Pyroxene thermometry reveals a temperature span of 850°C to 1280°C for the studied lavas while olivine–clinopyroxene thermometry yields a temperature range from 1040°–1160°C. The variation of temperature for the lava flows is ascribed to their normal cooling history after eruption.     

Stratigraphical framework of basaltic lavas in Torres Syncline main valley,southern Parana-Etendeka Volcanic Province

The Paraná-Etendeka Volcanic Province records the volcanism of the Early Cretaceous that precedes the fragmentation of the South-Gondwana supercontinent. Traditionally, investigations of these rocks prioritized the acquisition of geochemical and isotopic data, considering the volcanic stack as a monotonous succession of tabular flows. Torres Syncline is a tectonic structure located in southern Brazil and where the Parana-Etendeka basalts are well preserved. This work provides a detailed analysis of lithofacies and facies architecture, integrated to petrographic and geochemical data. We identified seven distinct lithofacies grouped into four facies associations related to different flow morphologies. The basaltic lava flows in the area can be divided into two contrasting units: Unit I - pahoehoe flow fields; and Unit II - simple rubbly flows. The first unit is build up by innumerous pahoehoe lava flows that cover the sandstones of Botucatu Formation. These flows occur as sheet pahoehoe, compound pahoehoe, and ponded lavas morphologies. Compound lavas are olivine-phyric basalts with intergranular pyroxenes. In ponded lavas and cores of sheet flows coarse plagioclase-phyric basalts are common. The first pahoehoe lavas are more primitive with higher contents of MgO. The emplacement of compound pahoehoe flows is related to low volume eruptions, while sheet lavas were emplaced during sustained eruptions. In contrast, Unit II is formed by thick simple rubbly lavas, characterized by a massive core and a brecciated/rubbly top. Petrographically these flows are characterized by plagioclase-phyric to aphyric basalts with high density of plagioclase crystals in the matrix. Chemically they are more differentiated lavas, and the emplacement is related to sustained high effusion rate eruptions. Both units are low TiO₂ and have geochemical characteristics of Gramado magma type. The Torres Syncline main valley has a similar evolution when compared to other Large Igneous Provinces, with compound flows at the base and simple flows in the upper portions. The detailed field work allied with petrography and geochemical data are extremely important to identify heterogeneities inside the volcanic pile and allows the construction of a detailed lithostratigraphical framework.     

Petrology and Geochemistry of the Bandas del Sur Formation, Las Canadas Edifice, Tenerife (Canary Islands)

The Bandas del Sur Formation preserves a Quaternary extra-calderarecord of central phonolitic explosive volcanism of the LasCañadas volcano at Tenerife. Volcanic rocks are bimodalin composition, being predominantly phonolitic pyroclastic deposits,several eruptions of which resulted in summit caldera collapse,alkali basaltic lavas erupted from many fissures around theflanks. For the pyroclastic deposits, there is a broad rangeof pumice glass compositions from phonotephrite to phonolite.The phonolite pyroclastic deposits are also characterized bya diverse, 7–8-phase phenocryst assemblage (alkali feldspar+ biotite + sodian diopside + titanomagnetite + ilmenite + nosean–haüyne+ titanite + apatite) with alkali feldspar dominant, in contrastto interbedded phonolite lavas that typically have lower phenocrystcontents and lack hydrous phases. Petrological and geochemicaldata are consistent with fractional crystallization (involvingthe observed phenocryst assemblages) as the dominant processin the development of phonolite magmas. New stratigraphicallyconstrained data indicate that petrological and geochemicaldifferences exist between pyroclastic deposits of the last twoexplosive cycles of phonolitic volcanism. Cycle 2 (0·85–0·57Ma) pyroclastic fall deposits commonly show a cryptic compositionalzonation indicating that several eruptions tapped chemically,and probably thermally stratified magma systems. Evidence formagma mixing is most widespread in the pyroclastic depositsof Cycle 3 (0·37–0·17 Ma), which includesthe presence of reversely and normally zoned phenocrysts, quenchedmafic glass blebs in pumice, banded pumice, and bimodal to polymodalphenocryst compositional populations. Syn-eruptive mixing eventsinvolved mostly phonolite and tephriphonolite magmas, whereasa pre-eruptive mixing event involving basaltic magma is recordedin several banded pumice-bearing ignimbrites of Cycle 3. Theperiodic addition and mixing of basaltic magma ultimately mayhave triggered several eruptions. Recharge and underplatingby basaltic magma is interpreted to have elevated sulphur contents(occurring as an exsolved gas phase) in the capping phonoliticmagma reservoir. This promoted nosean–haüyne crystallizationover nepheline, elevated SO₃ contents in apatite, and possiblyresulted in large, climatologically important SO₂ emissions. KEY WORDS: Tenerife; phonolite; crystal fractionation; magma mixing; sulphur-rich explosive eruptions     

Petrogenesis of basalt-comendite and basalt-pantellerite suites,Terceira, Azores,and some implications for the origin of ocean-island rhyolites

Petrogenetic modeling of the Recent lava succession of Santa Barbara and Pico Alto volcanoes and associated basaltic lavas indicates that there are two discrete lava series present, one erupted from the axial rift linking the two central volcanoes and one associated with monogenetic cones scattered around the flanks of Santa Barbara. The felsic lavas of both volcanoes are peralkaline and appear to be derived from associated basalts by fractional crystallization of an assemblage including essential amphibole. Trace element abundances in the felsic lavas, particularly those of Sr and REE, cannot be reconciled with an origin through partial melting of basaltic material at the base of the volcanic pile. The difference between the comenditic and pantelleritic differentiation trends of Santa Barbara and Pico Alto is attributed primarily to FO₂ control of the crystallizing assemblage, probably related to thermal dissociation of magmatic water in the Santa Barbara magma chamber. This effect may be augmented by minor differences in parent basaltic compositions, the Pico Alto pantellerites being derived from the rift basalts whereas the Santa Barbara comendites are derived from the off-rift basalts. A compositional gap between 54 and 64% silica content in the lavas is not present if the suite is extended to include co-magmatic hypabyssal xenoliths, leading to the inference that the gap in this and other bimodal suites results solely from a relative inability of magma of intermediate composition to erupt.     

Compositional evolution of the zoned calcalkaline magma chamber of Mount Mazama,Crater Lake,Oregon

The climactic eruption of Mount Mazama has long been recognized as a classic example of rapid eruption of a substantial fraction of a zoned magma body. Increased knowledge of eruptive history and new chemical analyses of 350 wholerock and glass samples of the climactic ejecta, preclimactic rhyodacite flows and their inclusions, postcaldera lavas, and lavas of nearby monogenetic vents are used here to infer processes of chemical evolution of this late Pleistocene — Holocene magmatic system. The 6845±50 BP climactic eruption vented 50 km³ of magma to form: (1) rhyodacite fall deposit; (2) welded rhyodacite ignimbrite; and (3) lithic breccia and zoned ignimbrite, these during collapse of Crater Lake caldera. Climactic ejecta were dominantly homogeneous rhyodacite (70.4±0.3% SiO₂), followed by subordinate andesite and cumulate scoriae (48–61% SiO₂). The gap in wholerock composition reflects mainly a step in crystal content because glass compositions are virtually continuous. Two types of scoriae are distinguished by different LREE, Rb, Th, and Zr, but principally by a twofold contrast in Sr content: High-Sr (HSr) and low-Sr (LSr) scoriae. HSr scoriae were erupted first. Trace element abundances indicate that HSr and LSr scoriae had different calcalkaline andesite parents; basalt was parental to some mafic cumulate scoriae. Parental magma compositions reconstructed from scoria wholerock and glass data are similar to those of inclusions in preclimactic rhyodacites and of aphyric lavas of nearby monogenetic vents.Preclimactic rhyodacite flows and their magmatic inclusions give insight into evolution of the climactic chamber. Evolved rhyodacite flows containing LSr andesite inclusions were emplaced between 30000 and 25000 BP. At 7015±45 BP, the Llao Rock vent produced a zoned rhyodacite pumice fall, then rhyodacite lava with HSr andesite inclusions. The Cleetwood rhyodacite flow, emplaced immediately before the climactic eruption and compositionally identical to climactic rhyodacite (volatile-free), contains different HSr inclusions from Llao Rock. The change from LSr to HSr inclusions indicates replenishment of the chamber with andesite magma, perhaps several times, in the latest Pleistocene to early Holocene.Modeling calculations and wholerock-glass relations suggest than: (1) magmas were derived mainly by crystallization differentiation of andesite liquid; (2) evolved preclimactic rhyodacite probably was derived from LSr andesite; (3) rhyodacites contain a minor component of partial melt from wall rocks, and (4) climactic and compositionally similar rhyodacites probably formed by mixing of evolved rhyodacite with HSr derivative liquid(s) after replenishment of the chamber with HSr andesite magma. Density considerations permit a model for growth and evolution of the chamber in which andesite recharge magma ponded repeatedly between cumulates and rhyodacite magma. Convective cooling of this andesite resulted in rapid crystallization and upward escape of buoyant derivative liquid which mixed with overlying, convecting rhyodacite. The evolved rhyodacites were erupted early in the chamber's history and(or) near its margins. Postcaldera andesite lavas may be hybrids composed of LSr cumulates mixed with remnant climactic rhyodacite. Younger postcaldera rhyodacite probably formed by fractionation of similar andesite and assimilation of partial melts of wallrocks.Uniformity of climactic rhyodacite suggests homogeneous silicic ejecta from other volcanoes resulted from similar replenishment-driven convective mixing. Calcalkaline pluton compositions and their internal zonation can be interpreted in terms of the Mazama system frozen at various times in its history.     

Chronological and geochemical study of lavas from the Chaîne des Puys,Massif Central,France: Evidence for crustal contamination

Datations of ancient lavas from the Chaîne des Puys through the ²³⁰Th-²³⁸U radioactive disequilibrium method confirm the eruption of several basaltic or slightly differentiated lavas around 40,000 years ago. The study of (²³⁰Th/²³²Th)₀ initial ratios of these lava flows clearly demonstrates the influence of a crustal contamination of magmas superimposed to crystal fractionation. This contamination probably affects many trace elements, in particular, U, Th and Sr. A model based on the (²³⁰Th/²³²Th)₀ initial ratio variations of non-contaminated lavas permits to consider that the first eruptions in the Chaîne des Puys could have occurred about 100,000 years ago.     

Petrology of the 1979 eruption of Soufriere volcano,St. Vincent,Lesser Antilles

Major element, trace element, and Sr isotope data are used to study the temporal variation in the chemistry of the ejecta from the 1979 eruption of Soufriere volcano, St. Vincent, and to compare the compositions of the 1979 and 1971/2 magmas. Both the 1971/2 and 1979 products were basaltic andesites almost identical in petrography. A small temporal variation in chemistry is apparent in the 1979 samples but these cannot be related to the 1971/2 lava by fractional crystallisation of phenocryst phases, and the two eruptions may therefore have sampled different batches of magma. ⁸⁷Sr/⁸⁶Sr ratios of the two magmas were identical within analytical error.Microprobe analyses of phenocryst phases and glasses from the 1979 ejecta are presented. Clinopyroxene phenocryst cores with very high Mg/Fe ratios indicate that the basaltic andesites are products of fractionation of magnesian parents. Such magmas are represented by lavas on St. Vincent similar to the microphyric alkali picrites found to the south in Grenada. A common origin for the basaltic andesites of both islands by fractional crystallisation of picritic magmas is suggested. Dacitic glass is abundant in the groundmass of scoria blocks from the eruption. It does not represent the liquid originally in equilibrium with the phenocryst phases, but rather this liquid modified by quench crystallisation. Published interpretations suggesting that dacitic glass compositions in tephra from eruptions of the Soufriere are evidence of mixed-magma eruptions are therefore rejected.     

Petrology and geochemistry of igneous inclusions in recent Merapi deposits: a window into the sub-volcanic plumbing system

Recent basaltic-andesite lavas from Merapi volcano contain abundant and varied igneous inclusions suggesting a complex sub-volcanic magmatic system for Merapi volcano. In order to better understand the processes occurring beneath Merapi, we have studied this suite of inclusions by petrography, geochemistry and geobarometric calculations. The inclusions may be classified into four main suites: (1) highly crystalline basaltic-andesite inclusions, (2) co-magmatic enclaves, (3) plutonic crystalline inclusions and (4) amphibole megacrysts. Highly crystalline basaltic-andesite inclusions and co-magmatic enclaves typically display liquid–liquid relationships with their host rocks, indicating mixing and mingling of distinct magmas. Co-magmatic enclaves are basaltic in composition and occasionally display chilled margins, whereas highly crystalline basaltic-andesite inclusions usually lack chilling. Plutonic inclusions have variable grain sizes and occasionally possess crystal layering with a spectrum of compositions spanning from gabbro to diorite. Plagioclase, pyroxene and amphibole are the dominant phases present in both the inclusions and the host lavas. Mineral compositions of the inclusions largely overlap with compositions of minerals in recent and historic basaltic-andesites and the enclaves they contain, indicating a cognate or ‘antelithic’ nature for most of the plutonic inclusions. Many of the plutonic inclusions plot together with the host basaltic-andesites along fractional crystallisation trends from parental basalt to andesite compositions. Results for mineral geobarometry on the inclusions suggest a crystallisation history for the plutonic inclusions and the recent and historic Merapi magmas that spans the full depth of the crust, indicating a multi-chamber magma system with high amounts of semi-molten crystalline mush. There, crystallisation, crystal accumulation, magma mixing and mafic recharge take place. Comparison of the barometric results with whole rock Sr, Nd, and Pb isotope data for the inclusions suggests input of crustal material as magma ascends from depth, with a significant late addition of sedimentary material from the uppermost crust. The type of multi-chamber plumbing system envisaged contains large portions of crystal mush and provides ample opportunity to recycle the magmatic crystalline roots as well as interact with the surrounding host lithologies.     

Cumulate xenoliths from St. Vincent, Lesser Antilles Island Arc: a window into upper crustal differentiation of mantle-derived basalts

In order to shed light on upper crustal differentiation of mantle-derived basaltic magmas in a subduction zone setting, we have determined the mineral chemistry and oxygen and hydrogen isotope composition of individual cumulus minerals in plutonic blocks from St. Vincent, Lesser Antilles. Plutonic rock types display great variation in mineralogy, from olivine–gabbros to troctolites and hornblendites, with a corresponding variety of cumulate textures. Mineral compositions differ from those in erupted basaltic lavas from St. Vincent and in published high-pressure (4–10 kb) experimental run products of a St. Vincent high-Mg basalt in having higher An plagioclase coexisting with lower Fo olivine. The oxygen isotope compositions (δ¹⁸O) of cumulus olivine (4.89–5.18‰), plagioclase (5.84–6.28‰), clinopyroxene (5.17–5.47‰) and hornblende (5.48–5.61‰) and hydrogen isotope composition of hornblende (δD = −35.5 to −49.9‰) are all consistent with closed system magmatic differentiation of a mantle-derived basaltic melt. We employed a number of modelling exercises to constrain the origin of the chemical and isotopic compositions reported. δ¹⁸O_Olivine is up to 0.2‰ higher than modelled values for closed system fractional crystallisation of a primary melt. We attribute this to isotopic disequilibria between cumulus minerals crystallising at different temperatures, with equilibration retarded by slow oxygen diffusion in olivine during prolonged crustal storage. We used melt inclusion and plagioclase compositions to determine parental magmatic water contents (water saturated, 4.6 ± 0.5 wt% H₂O) and crystallisation pressures (173 ± 50 MPa). Applying these values to previously reported basaltic and basaltic andesite lava compositions, we can reproduce the cumulus plagioclase and olivine compositions and their associated trend. We conclude that differentiation of primitive hydrous basalts on St. Vincent involves crystallisation of olivine and Cr-rich spinel at depth within the crust, lowering MgO and Cr₂O₃ and raising Al₂O₃ and CaO of residual melt due to suppression of plagioclase. Low density, hydrous basaltic and basaltic andesite melts then ascend rapidly through the crust, stalling at shallow depth upon water saturation where crystallisation of the chemically distinct cumulus phases observed in this study can occur. Deposited crystals armour the shallow magma chamber where oxygen isotope equilibration between minerals is slowly approached, before remobilisation and entrainment by later injections of magma.     

Rare earth element geochemistry of the Betts Cove ophiolite,Newfoundland: complexities in ophiolite formation

The Betts Cove ophiolite includes the components of typical ocean crust: pillow lavas, sheeted dikes, gabbros and ultramafics. However, the trace element geochemistry of basaltic rocks is unusual. Three geochemical units are recognized within the lava and dike members. Within the pillow lavas, the geochemical units correspond to stratigraphic units. Upper lavas have ‘normal’ (i.e., typical for ocean floor basalts) TiO₂ contents (0.75 to 2.0 wt%), heavy rare earth elements (HREE) values in the range 6–20× chondrites and chondrite-normalized REE patterns with relative LREE depletion. Intermediate lavas have TiO₂ contents between 0.30 and 0.50 wt%, HREE contents from 4–7× chondrites and extreme relative LREE depletion. Lower lavas have anomalously low TiO₂ contents (<0.30 wt%) and unusual convex-downwards REE patterns with REE abundances around 2–5 × chondrite. These geochemical differences can be explained if the three groups were derived from different mantle sources. Independent mantle sources for the three units are consistent with their different ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios varying at 480 m.y.B.P. from 0.51222 in a lower lava to 0.51238 in an upper lava. The upper lavas may be partial melts of a source similar in composition to that of modern MORB, the intermediate lavas may be from a very depleted oceanic mantle (second stage melt), and the lower lavas may have formed by melting an extremely depleted mantle that had been invaded by a LREE-enriched fluid. A possible tectonic environment where these different sources could be juxtaposed is a back-arc or inter-arc basin.     

Geochronology and evolution of quaternary volcanism at the Keli Highland,Greater Caucasus

The paper reports newly obtained stratigraphic, petrographic, and isotope-geochronological data on modern moderately acid lavas from the Keli Highland at the Greater Caucasus and presents a geological map of the territory, in which 35 volcanoes active in Late Quaternary time were documented by the authors. The total duration of volcanic activity at the highland was estimated at 250 ka. The volcanic activity was discrete and occurred in three phases: Middle Neopleistocene (245−170 ka), Late Neopleistocene (135−70 ka), and Late Neopleistocene-Holocene (<30 ka). Newly obtained lines of evidence indicate that certain volcanoes erupted in the latest Neopleistocene-Holocene. The first phase of volcanic activity was connected mainly with lava volcanoes, and eruptions during the later phases of volcanic activity in this part of the Greater Caucasus produced mainly lavas. The most significant eruptions are demonstrated to occur in the territory during the second phase. The major evolutionary trends of volcanic processes during the final phase in the Keli Highland are determined. It was also determined that the overwhelming majority of volcanoes that were active less than 30 ka B.P. are spatially restricted to long-liven local magmatic zones, which were active during either all three or only the final two phases of activity. These parts of the territory are, perhaps, the most hazardous in terms of volcanic activity.     

Evolution of Mount Cameroon volcanism: Geochemistry,mineral chemistry and radiogenic isotopes (Pb,Sr, Nd)

Mount Cameroon volcano has erupted several times in the 20th Century with documented eruptions in 1909, 1922, 1954, 1959, 1982, 1999 and 2000. Evidence of historic volcanism is represented by several older lava flows and lahar deposits around the flanks of the volcano. This study aims to assess the evolution of Mount Cameroon volcanism through its eruptive history via interpretation of mineralogical, whole rock geochemical and Pb, Sr, Nd isotope data generated from historic and recent lava flows. In this study, samples were collected from the 1959, 1982, 1999 and 2000 eruptions and from several historic eruption sites with unknown eruption dates.Evaluation of major and trace element data demonstrates that Mount Cameroon is geotectonically associated with within-plate Ocean Island Basalt Settings. More than 90% of the studied historic lavas (n ​= ​29) classify as tephrites and basanites whereas the modern lavas (n ​= ​38) are predominantly trachybasalts, demonstrating evolution from primitive to evolved lavas over time typically in response to fractional crystallization. Petrographically, the lavas are porphyritic with main mineral phases being olivine, clinopyroxene, plagioclase feldspars and Fe–Ti–Cr oxides. The 1982 lavas are predominantly aphyric and dominated by lath-shaped flow-aligned plagioclase in the groundmass. Olivine chemistry shows variable forsterite compositions from Fo_60–89. Clinopyroxenes vary from diopside through augite to titanaugite with chemical composition ranges from Wo₄₅En₃₂Fs₇ to Wo₅₁En₄₇Fs₁₇. Plagioclase feldspars vary from labradorite (An_56–70) to bytownite (An_80–87). For the Fe–Ti–Cr oxides, calculated ulvöspinel component shows a wide variation from ulv_38–87. CIPW-normative classification on the Di-Ol-Hy-Qz-Ne system shows that all Mount Cameroon lavas are nepheline-normative (Ne ranges from 4.20 wt.% to 11.45 ​wt.%).Radiogenic isotope data demonstrate that Mount Cameroon lavas are HIMU (or high μ ​= ​²³⁸U/²⁰⁴Pb), characterized by ²⁰⁶Pb/²⁰⁴Pb ​= ​20.19–20.46, ²⁰⁷Pb/²⁰⁴Pb ​= ​15.63–15.69, ²⁰⁸Pb/²⁰⁴Pb ​= ​40.01–40.30, ⁸⁷Sr/⁸⁶Sr ​= ​0.70322–0.70339 (ε_Sr ​= ​−21.37 to −18.96) and ¹⁴³Nd/¹⁴⁴Nd ​= ​0.51276–0.51285 (ε_Nd ​= ​+2.29 to +4.05). The historic lavas show stronger HIMU signature relative to the modern lavas, suggesting evolution towards less HIMU signatures over time. This study has revealed that Mount Cameroon volcanism has evolved from primitive magmas characterized by stronger HIMU signatures with high ^206/204Pb and ^208/204Pb isotopes, low SiO₂ and high Mg, Ni, Cr content towards lower HIMU signatures with relatively higher SiO₂, lower Mg, Cr and Ni compositions. The geochemical and isotopic changes, which account for the evolution of magmatism on Mount Cameroon occur over long periods of time because all the modern lavas erupted within the last 100 years are isotopically homogeneous, with very limited variation in SiO₂ compositions.     

Sugarloaf Mountain,central Arizona,USA: A small-scale example of Miocene basalt-rhyolite magma mixing to yield andesitic magmas

Sugarloaf Mountain is a 200-m high volcanic landform in central Arizona, USA, within the transition from the southern Basin and Range to the Colorado Plateau. It is composed of Miocene alkalic basalt (47.2–49.1?wt.% SiO₂; 6.7–7.7?wt.% MgO) and overlying andesite and dacite lavas (61.4–63.9?wt.% SiO₂; 3.5–4.7?wt.% MgO). Sugarloaf Mountain therefore offers an opportunity to evaluate the origin of andesite magmas with respect to coexisting basalt. Important for evaluating Sugarloaf basalt and andesite (plus dacite) is that the andesites contain basaltic minerals olivine (cores Fo_76-86) and clinopyroxene (～Fs_9-18Wo_35-44) coexisting with Na-plagioclase (An_48-28Or_1.4–7), quartz, amphibole, and minor orthopyroxene, biotite, and sanidine. Noteworthy is that andesite mineral textures include reaction and spongy zones and embayments in and on Na-plagioclase and quartz phenocrysts, where some reacted Na-plagioclases have higher-An mantles, plus some similarly reacted and embayed olivine, clinopyroxene, and amphibole phenocrysts.Fractional crystallization of Sugarloaf basaltic magmas cannot alone yield the andesites because their ～61 to 64?wt.% SiO₂ is attended by incompatible REE and HFSE abundances lower than in the basalts (e.g., Ce 77–105 in andesites vs 114–166?ppm in basalts; Zr 149–173 vs 183–237; Nb 21–25 vs 34–42). On the other hand, andesite mineral assemblages, textures, and compositions are consistent with basaltic magmas having mixed with rhyolitic magmas, provided the rhyolite(s) had relatively low REE and HFSE abundances. Linear binary mixing calculations yield good first approximation results for producing andesitic compositions from Sugarloaf basalt compositions and a central Arizona low-REE, low-HFSE rhyolite. For example, mixing proportions 52:48 of Sugarloaf basalt and low incompatible-element rhyolite yields a hybrid composition that matches Sugarloaf andesite well ? although we do not claim to have exact endmembers, but rather, viable proxies. Additionally, the observed mineral textures are all consistent with hot basalt magma mixing into rhyolite magma. Compositional differences among the phenocrysts of Na-plagioclase, clinopyroxene, and amphibole in the andesites suggest several mixing events, and amphibole thermobarometry calculates depths corresponding to 8–16?km and 850° to 980?°C. The amphibole P-T observed for a rather tight compositional range of andesite compositions is consistent with the gathering of several different basalt-rhyolite hybrids into a homogenizing ‘collection' zone prior to eruptions. We interpret Sugarloaf Mountain to represent basalt-rhyolite mixings on a relatively small scale as part of the large scale Miocene (～20 to 15 Ma) magmatism of central Arizona. A particular qualification for this example of hybridization, however, is that the rhyolite endmember have relatively low REE and HFSE abundances.     

Mafic magmas from Mount Baker in the northern Cascade arc,Washington: probes into mantle and crustal processes

Five mafic lava flows located on the southern flank of Mount Baker are among the most primitive in the volcanic field. A comprehensive dataset of whole rock and mineral chemistry reveals the diversity of these mafic lavas that come from distinct sources and have been variably affected by ascent through the crust. Disequilibrium textures present in all of the lavas indicate that crustal processes have affected the magmas. Despite this evidence, mantle source characteristics have been retained and three primitive endmember lava types are represented. These include (1) modified low-K tholeiitic basalt (LKOT-like), (2) typical calc-alkaline (CA) lavas, and (3) high-Mg basaltic andesite and andesite (HMBA and HMA). The Type 1 endmember, the basalt of Park Butte (49.3–50.3 wt% SiO₂, Mg# 64–65), has major element chemistry similar to LKOT found elsewhere in the Cascades. Park Butte also has the lowest overall abundances of trace elements (with the exception of the HREE), indicating it is either derived from the most depleted mantle source or has undergone the largest degree of partial melting. The Type 2 endmember is represented by the basalts of Lake Shannon (50.7–52.6 wt% SiO₂, Mg# 58–62) and Sulphur Creek (51.2–54.6 wt% SiO₂, Mg# 56–57). These two lavas are comparable to calc-alkaline rocks found in arcs worldwide and have similar trace element patterns; however, they differ from each other in abundances of REE, indicating variation in degree of partial melting or fractionation. The Type 3 endmember is represented by the HMBA of Tarn Plateau (51.8–54.0 wt% SiO₂, Mg# 68–70) and the HMA of Glacier Creek (58.3–58.7 wt% SiO₂, Mg# 63–64). The strongly depleted HREE nature of these Type 3 units and their decreasing Mg# with increasing SiO₂ suggests fractionation from a high-Mg basaltic parent derived from a source with residual garnet. Another basaltic andesite unit, Cathedral Crag (52.2–52.6 wt% SiO₂, Mg# 55–58), is an Mg-poor differentiate of the Type 3 endmember. The calc-alkaline lavas are least enriched in a subduction component (lowest H₂O, Sr/P_N, and Ba/Nb), the LKOT-like lavas are intermediate (moderate Sr/P_N and Ba/Nb), and the HMBA are most enriched (highest H₂O, Sr/P_N and Ba/Nb). The generation of the LKOT-like and calc-alkaline lavas can be successfully modeled by partial melting of a spinel lherzolite with variability in composition of slab flux and/or mantle source depletion. The HMBA lavas can be successfully modeled by partial melting of a garnet lherzolite with slab flux compositionally similar to the other lava types, or less likely by partial melting of a spinel lherzolite with a distinctly different, HREE-depleted slab flux.     

The Cerro Morado Andesites: Volcanic history and eruptive styles of a mafic volcanic field from northern Puna, Argentina

The Upper Miocene Cerro Morado Andesites constitutes a mafic volcanic field (100 km²) composed of andesite to basaltic andesite rocks that crop out 75 km to the east from the current arc, in the northern Puna of Argentina. The volcanic field comprises lavas and scoria cones resulting from three different eruptive phases developed without long interruptions between each other. Lavas and pyroclastic rocks are thought to be sourced from the same vents, located where orogen-parallel north-south faults crosscut transverse structures.The first eruptive phase involved the effusion of extensive andesitic flows, and minor Hawaiian-style fountaining which formed subordinate clastogenic lavas. The second phase represents the eruption of slightly less evolved andesite lavas and pyroclastic deposits, only distributed to the north and central sectors of the volcanic field. The third phase represents the discharge of basaltic andesite magmas which occurred as both pyroclastic eruptions and lava effusion from scattered vents distributed throughout the entire volcanic field. The interpreted facies model for scoria cones fits well with products of typical Strombolian-type activity, with minor fountaining episodes to the final stages of eruptions.Petrographic and chemical features suggest that the andesitic units (SiO₂ > 57%) evolved by crystal fractionation. In contrast, characteristics of basaltic andesite rocks are inconsistent with residence in upper-crustal chambers, suggesting that batches of magmas with different origins or evolutive histories arrived at the surface and erupted coevally.Based on the eruptive styles and lack of volcanic quiescence gaps between eruptions, the Cerro Morado Andesites can be classified as a mafic volcanic field constructed from the concurrent activity of several small, probably short-lived, monogenetic centers.