High-titania alkali-olivine basalts of north-central Oregon,U.S.A.

In north-central Oregon numerous small flows of alkali-olivine basalt occur in the Oligocene to early Miocene John Day Formation. Chemically, these basalts are characterized by relatively low SiO₂ and K₂O and very high TiO₂ and iron. Fifteen analysed specimens (44 to 48 percent SiO₂) have an average of 3.6 percent TiO₂ and 15 percent total iron. The average composition of the Oregon basalts compares closely with the average hawaiite of the Hawaiian Islands, differing only in having slightly higher iron and slightly lower SiO₂ and total alkalis. Closely associated flows of trachyandesite and quartz latite are chemically related to the basalts and probably formed by differentiation of an alkali-olivine basalt magma.Typical basalt specimens have 10 to 15 percent of modal olivine, interstitial alkali feldspar, and abundant clay minerals and chlorophaeite. Textures are subophitic or intersertal and phenocrysts are rare. Plagioclase laths are slightly zoned and range in composition from An₆₈ to An₄₄. Purplish-brown titaniferous augite is the only pyroxene, and ilmenite is the dominant opaque mineral.Distinct differences in composition and age, and the lack of transitional varieties indicate that these basalts are unrelated to the younger Columbia River basalts. They presumably represent a separate parent magma of alkalic affinity that was generated independently within the mantle.     

Density,Viscosity and Velocity (Ascent Rate) of Alkaline Magmas

Three distinct alkaline magmas, represented by shonkinite, lamprophyre and alkali basalt dykes, characterize a significant magmatic expression of rift-related mantle-derived igneous activity in the Mesoproterozoic Prakasam Alkaline Province, SE India. In the present study we have estimated emplacement velocities (ascent rates) for these three varied alkaline magmas and compared with other silicate magmas to explore composition control on the ascent rates. The alkaline dykes have variable widths and lengths with none of the dykes wider than 1 m. The shonkinites are fine- to medium-grained rocks with clinopyroxene, phologopite, amphibole, K-feldspar perthite and nepheline as essential minerals. They exhibit equigranular hypidiomorphic to foliated textures. Lamprophyres and alkali basalts characteristically show porphyritic textures. Olivine, clinopyroxene, amphibole and biotite are distinct phenocrysts in lamprophyres whereas olivine, clinopyroxene and plagioclase form the phenocrystic mineralogy in the alkali basalts. The calculated densities [2.54–2.71 g/cc for shonkinite; 2.61–2.78 g/cc for lamprophyre; 2.66–2.74 g/cc for alkali basalt] and viscosities [3.11–3.39 Pa s for shonkinite; 3.01–3.28 Pa s for lamprophyre; 2.72–3.09 Pa s for alkali basalt] are utilized to compute velocities (ascent rates) of the three alkaline magmas. Since the lamprophyres and alkali basalts are crystal-laden, we have also calculated effective viscosities to infer crystal control on the velocities. Twenty percent of crystals in the magma increase the viscosity by 2.7 times consequently decrease ascent rate by 2.7 times compared to the crystal-free magmas. The computed ascent rates range from 0.11–2.13 m/sec, 0.23–2.77 m/sec and 1.16–2.89 m/sec for shonkinite, lamprophyre and alkali basalt magmas respectively. Ascent rates increase with the width of the dykes and density difference, and decrease with magma viscosity and proportion of crystals. If a constant width of 1 m is assumed in the magma-filled dyke propagation model, then the sequence of emplacement velocities in the decreasing order is alkaline magmas (4.68–15.31 m/sec) > ultramafic-mafic magmas (3.81–4.30 m/sec) > intermediate-felsic magmas (1.76–2.56 m/sec). We propose that SiO₂ content in the terrestrial magmas can be modeled as a semi-quantitative “geospeedometer” of the magma ascent rates.     

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.     

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.     

Andesites from northeastern Kanaga Island,Aleutians

Kanaga island is located in the central Aleutian island arc. Northeastern Kanaga is a currently active late Tertiary to Recent calc-alkaline volcanic complex. Basaltic andesite to andesite lavas record three episodes (series) of volcanic activity. Series I and Series II lavas are all andesite while Series III lavas are basaltic andesite to andesite. Four Series II andesites contain abundant quenched magmatic inclusions ranging in composition from high-MgO low-alumina basalt to low-MgO highalumina basalt. The spectrum of lava compositions is due primarily to fractional crystallization of a parental low-MgO high-alumina basalt but with variable degrees of crustal contamination and magma mixing. The earliest Series I lavas represent mixing between high-alumina basalt and silicic andesite with maximum SiO₂ contents of 65–67 wt %. Later Series I and all Series II lavas are due to mixing of andesite magmas of similar composition. The maximum SiO₂ content of the pre-mixed andesites magmas is estimated at 60–63 wt %. The youngest lavas (Series III) are all non-mixed and have maximum estimated SiO₂ contents of 59 wt %. The earliest Series I lavas contain a significant crustal component while all later lavas do not. It is concluded that the maximum SiO₂ contents of silicic magmas, the contribution of crustal material to silicic magma generation, and the role of magma mixing all decrease with time. Furthermore, silicic magmas generated by fractional crystallization at this volcanic center have a maximum SiO₂ content of 63 wt %. All of these features have also been documented at the central Aleutian Cold Bay Volcanic Center (Brophy 1987). Based on data from these two centers a model of Aleutian calc-alkaline magma chamber development is proposed. The main features are: (1) a single low pressure magma chamber is continuously supplied by primitive low-alumina basalt; (2) non-primary high-alumina basalt is formed along the chamber margins by selective gravitational settling of olivine and clinopyroxene and retention of plagioclase; (3) sidewall crystallization accompanied by crustal melting produces buoyant silicic (>63 wt % SiO₂) liquids that pond at the top of the chamber, and; (4) continued sidewall crystallization, now isolated from the chamber wall, produces silicic liquids with 63 wt % SiO₂ that increase the thickness and lowers the overall SiO₂ content of the upper silicic zone. It is suggested that the maximum SiO₂ content of 63% imposed on fractionation-generated magmas is due to a rheological barrier that prohibits the extraction of more silicic liquids from a crystal-liquid mush along the chamber wall.     

Quantitative Untersuchungen mit der Elektronen-Mikrosonde an Pyroxenen aus Basalten und Peridotit-Einschlüssen

The chemical composition of the pyroxenes and olivines of 12 basaltic rocks and 5 lherzolite nodules was determined quantitatively by electron micro-probe analysis. The composition of the pyroxenes depends on the type of basalt in which they occur. Tholeiitic basalts with normative quartz contain three pyroxenes: orthorombic pyroxenes, pigeonites and augites. All pyroxene phases are zoned and do not show any exsolution. Their Ti and Al contents (Ca-Tschermaks and Ti-augite molecules) are small. All pyroxene phases were formed under disequilibrium with each other and with the melt because of rapid quenching. The sequence of crystallization: orthopyroxene—pigeonite—augite could be established by their Cr content.The alkali olivine basalts undersatured in SiO₂ and the olivine nephelinites are characterized by Ti and Al-rich clinopyroxenes. The distribution of Ti and Al in the pyroxenes of the alkali olivine basalts shows a differentiation trend from the cores of the phenocrysts to their outer zones and to the crystals of the ground mass. Thereby the Ca-Tschermaks molecule is being replaced more and more by the Ti-augite molecule. The Ti content of the pyroxenes of the olivine nephelinites decreases in the last stage of differentiation because simultaneously increasing amounts of titaniferous magnetite crystallize.The pyroxenes of lherzolite peridotite nodules are characterized by high Al and low Ti contents which differ according to the type of basalt (alkali olivine basalt or olivine nephelinite) in which the nodules occur. The homogeneous distribution of the elements within the single grains indicates crystallization under equlibrium conditions. The conditions of their formation are comparable to those of Al-pyroxene peridotites in the upper mantle. The composition of pyroxenes of early accumulates of alkali basaltic melts differ from those of peridotite nodules. Therefore lherzolite nodules can be taken as residues of deeper peridotite masses.     

Phase relations of a high-Mg basalt from the Aleutian Island Arc: Implications for primary island arc basalts and high-Al basalts

Many volcanic centers in the Aleutian Islands have erupted lavas that range in composition from high-Mg basalt (MgO>9 wt%) to more fractionated and voluminous high-Al basalts and basaltic andesites. The petrogenetic relationships between these rock types and the composition of primary magmas has been vigorously debated. The phase relations of a typical high-Mg basalt from the Makushin volcanic field on Unalaska Island provide important constraints on petrogenetic models. Results of one-atmosphere and moderate-to high-pressure (5–20 kb) anhydrous experiments are similar to results obtained from primitive MORB. At low pressures olivine is the liquidus phase joined by plagioclase and clinopyroxene at progressively lower temperatures. Clinopyroxene is the second phase to crystallize at pressures greater than 5 kb and replaces olivine on the liquidus at approximately 10 kb. Above 10 kb the liquidus pyroxene is aluminous augite and orthopyroxene is the second phase to crystallize. Glasses in equilibrium with olivine and clinopyroxene at intermediate-pressure (5 to 10 kb) are similar in composition to high-Al basalt. Plagioclase is not involved and most likely does not become a liquidus phase until the liquid has evolved significantly. Although our studies do not confirm the primary nature of high-Mg basalts they do support a model in which high-Al basalts are generated by moderate amounts of crystal fractionation from more primitive (high Mg/Mg+Fe, lower Al₂O₃) basaltic magmas near the arc crust-mantle boundary.Abbreviations Ol olivine - Cpx Clinopyroxene - Pl plagioclase - L liquid - Sp spinel - Pig pigeonite - Opx Orthopyroxene     

Aleutian tholeiitic and calc-alkaline magma series I: The mafic phenocrysts

Diagnostic mafic silicate assemblages in a continuous spectrum of Aleutian volcanic rocks provide evidence for contrasts in magmatic processes in the Aleutian arc crust. Tectonic segmentation of the arc exerts a primary control on the variable mixing, fractional crystallization and possible assimilation undergone by the magmas. End members of the continuum are termed calc-alkaline (CA) and tholeiitic (TH). CA volcanic rocks (e.g., Buldir and Moffett volcanoes) have low FeO/MgO ratios and contain compositionally diverse phenocryst populations, indicating magma mixing. Their Ni and Cr-rich magnesian olivine and clinopyroxene come from mantle-derived mafic olivine basalts that have mixed with more fractionated magmas at mid-to lower-crustal levels immediately preceding eruption. High-Al amphibole is associated with the mafic end member. In contrast, TH lavas (e.g., Okmok and Westdahl volcanoes) have high FeO/MgO ratios and contain little evidence for mixing. Evolved lavas represent advanced stages of low pressure crystallization from a basaltic magma. These lavas contain groundmass olivine (FO 40–50) and lack Ca-poor pyroxene. Aleutian volcanic rocks with intermediate FeO/MgO ratios are termed transitional tholeiitic (TTH) and calc-alkaline (TCA). TCA magmas are common (e.g., Moffett, Adagdak, Great Sitkin, and Kasatochi volcanoes) and have resulted from mixing of high-Al basalt with more evolved magmas. They contain amphibole (high and low-Al) or orthopyroxene or both and are similar to the Japanese hypersthene-series. TTH magmas (e.g., Okmok and Westdahl) contain orthopyroxene or pigeonite or both, and show some indication of upper crustal mixing. They are mineralogically similar to the Japanese pigeonite-series. High-Al basalt lacks Mg-rich mafic phases and is a derivative magma produced by high pressure fractionation of an olivine tholeiite. The low pressure mineral assemblage of high-Al basalt results from crystallization at higher crustal levels.     

Indirect crustal contamination: evidence from isotopic and chemical disequilibria in minerals from alkali basalts and nephelinites from northern Tanzania

 Alkali basalts and nephelinites from the volcanic province of northern Tanzania contain pyroxene and nepheline that show evidence for chemical and/or isotopic disequilibria with their host magmas. Olivine, pyroxene, nepheline and plagioclase all appear to be partially xenocrystic in origin. Five whole rock/mineral separate pairs have been analyzed for Sr, Nd, and Pb isotopic compositions. The ²⁰⁶Pb/²⁰⁴Pb ratios are distinct by as much as 20.94 (whole rock) vs. 19.10 (clinopyroxene separate). The Sr and Nd isotopic disequilibria vary from insignificant in the case of nepheline, to Δ ⁸⁷Sr/⁸⁶Sr of 0.0002 and Δɛ_Nd of 0.7 in the case of clinopyroxene. The mineral chemistry of 25 samples indicates the ubiquitous presence of minerals that did not crystallize from a liquid represented by the host rock. The northern Tanzanian magmas are peralkaline and exhibit none of the xenocrystic phases expected from crustal assimilation. The disequilibria cannot be the result of mantle source variations. Rather the xenocrystic phases present appear to have been derived from earlier alkali basaltic rocks or magmas that were contaminated by the crust. Material from this earlier magma was then mixed with batches of magma that subsequently erupted on the surface. Disequilibrium in volcanic rocks has potentially serious consequences for the use of whole rock data to identify source reservoirs. However, mass balance calculations reveal that the ²⁰⁶Pb/²⁰⁴Pb isotopic compositions of the erupted lavas were changed by less than 0.25% as a result of this indirect crustal contamination. Received: 15 February 1995 / Accepted: 4 May 1996     

Petrology of alkali basalts of Zlot, Timok Magmatic Complex (Eastern Serbia)

Alkali basalts were discovered in the Timok Magmatic Complex only in a borehole near Zlot. They are composed of plagioclase and clinopyroxene phenocrysts lying in intersertal to pilotaxitic groundmass. The characteristic feature of these rocks is the high content of needle shaped magnetite.

Various disequilibrium features in alkali basalt of Zlot reflect complex convection effects and recharge, most probably in a shallow magma chamber. Major and trace elements data indicate that alkali basalts of Zlot originated from magmas deriving from metasomatized mantle wedge above a subducting and dehydrating plate. However the investigated rocks did not originate from primary magmas, but from a magma which has undergone considerable fractional crystallization.     

Assigning a magmatically defined tectonic environment to Chitradurga metabasalts,India, by geochemical methods

The major and trace-element patterns in a set of 45 analyses of the Precambrian Chitradurga metabasalts have been interpreted by geochemical methods to classify the magma-types and to determine the tectonic environment of eruption.During amphibolitization of the tholeiites, the order of relative chemical stability is: SiO₂ > MgO > Al₂O₃ > FeO > CaO > Na₂O > K₂O > P₂O₅. On the ACFN plot the Chitradurga amphibolites approximate the unaltered basalts in their N component, show considerable depletion in F and A, and enrichment in the C components. With respect to the Keweenawan metadomains (pumpellyite and epidote), the Chitradurga amphibolites show considerable enrichment in N and depletion in the C constituents. The calc-alkaline (mol.props.) index, SiO₂ (wt.%) and “F”MA plots have shown the differentiation of the parent olivine normative tholeiite through the transitional calc-alkalic basalts to basaltic andesites; the ferrofemic index being 67.Discriminant functional analysis of the major-element patterns has classified the magma-types into ocean-floor basalts (9 analyses) and the volcanic arc series containing low-potassium tholeiites (24 analyses), calc-alkalic basalts (6 analyses) and basaltic andesites (6 analyses). The effective discrimination of the ocean-floor basalts from low-potassium tholeiites is accomplished due to the relatively low eigenvalues in functions F₁ and F₂ for SiO₂, K₂O and high values for MgO, TiO₂ in the former as compared to the latter. The low-K tholeiites are discriminated from calc-alkalic and basaltic andesites by the gradational increase in eigenvalues for K₂O, SiO₂ and Al₂O₃ in functions F₂ and F₃. The discriminant analyses of the trace-element patterns have classified the ocean-floor basalts from low-K tholeiites on TiCr, TiZr and Ti(× 10^?2)ZrY(× 3) plots. The TiO₂K₂OP₂O₅ plot has discriminated ocean-floor basalts, low-K tholeiites and the calc-alkalic group containing the basaltic andesite members. Thus the discriminant analysis of the major and trace-element patterns have shown noteworthy consistency, thereby attesting to the high success rate of classification.The Ca-Mg rich, low SiO₂, K₂O and alumina, olivine normative characteristics, and the normative pyroxene content of 36.15–45.88% of the ocean-floor basalts compare closely with those of the oceanic magma type of the Dalma volcanic suite of the north-eastern part of the Precambrian Indian shield of Bihar. These compositional features indicate their mantle origin, amphibolite and plagioclase—pyrolite assemblage of the upper mantle and relatively low-temperature, moderate pressure and hydrous environment of pyrolite.The presence of ocean-floor basalts at Chitradurga implies the existence of an oceanic rise and their eruption through its axial rift region. The mean Ti content (0.77%) of ocean-floor basalts compares closely with that of the Dalma suite (0.76%). The low-alumina content indicates faster spreading of the ocean floor.Identification of the magma-types of volcanic arc series containing a wide range of Zr and Y is attributed to quartz-normative fractionation of the magma and its differentiation to calc-alkalic and basaltic andesite members due to incorporation of sialic material by accretion in the marginal regions of the volcanic belt.Attention is focussed on the synonymous tectonic evolutionary trends of the two typical volcanic belts of the two geographically widely separated regions of the Indian Precambrian shield; the basis being: (1) low-alumina, enriched Ca-Mg and almost identical concentrations of Ti in the ocean-floor magma type, and (2) the presence of a pronounced volcanic arc magma type in the Chitradurga area and two analyses of a volcanic arc magma type in the Dalma area.     

Magma mixing in the San Francisco Volcanic Field,AZ

A wide variety of rock types are present in the O'Leary Peak and Strawberry Crater volcanics of the Pliocene to Recent San Francisco Volcanic Field (SFVF), AZ. The O'Leary Peak flows range from andesite to rhyolite (56–72 wt % SiO₂) and the Strawberry Crater flows range from basalt to dacite (49–64 wt % SiO₂). Our interpretation of the chemical data is that both magma mixing and crustal melting are important in the genesis of the intermediate composition lavas of both suites. Observed chemical variations in major and trace elements can be modeled as binary mixtures between a crustal melt similar to the O'Leary dome rhyolite and two different mafic end-members. The mafic end-member of the Strawberry suite may be a primary mantle-derived melt. Similar basalts have also been erupted from many other vents in the SFVF. In the O'Leary Peak suite, the mafic end-member is an evolved (low Mg/(Mg+ Fe)) basalt that is chemically distinct from the Strawberry Crater and other vent basalts as it is richer in total Fe, TiO₂, Al₂O₃, MnO, Na₂O, K₂O, and Zr and poorer in MgO, CaO, P₂O₅, Ni, Sc, Cr, and V. The derivative basalt probably results from fractional crystallization of the more primitive, vent basalt type of magma. This evolved basalt occurs as xenolithic (but originally magmatic) inclusions in the O'Leary domes and andesite porphyry flow. The most mafic xenolith may represent melt that mixed with the O'Leary dome rhyolite resulting in andesite preserved as other xenoliths, a pyroclastic unit (Qoap), porphyry flow (Qoaf) and dacite (Darton Dome) magmas. Thermal constraints on the capacity of a melt to assimilate (and melt) a volume of solid material require that melt mixing and not assimilation has produced the observed intermediate lavas at both Strawberry Crater and O'Leary Peak. Textures, petrography, and mineral chemistry support the magma mixing model. Some of the inclusions have quenched rims where in contact with the host. The intermediate rocks, including the andesite xenoliths, contain xenocrysts of quartz, olivine and oligoclase, together with reversely zoned plagioclase and pyroxene phenocrysts. The abundance of intermediate volcanic rocks in the SFVF, as observed in detail at O'Leary Peak and Strawberry Crater, is due in part to crustal recycling, the result of basalt-driven crustal melting and the subsequent mixing of the silicic melts with basalts and derivative magmas.     

The geochemistry and petrogenesis of dolerites and gabbros from the Tertiary central volcanic complex of Slieve Gullion,North East Ireland

Basaltic magmas emplaced into the root zone of the Slieve Gullion volcano have crystallised to rocks varying in texture from dolerite to gabbro. A mineralogical variation from olivine bearing to quartz bearing varieties has been recorded and with the presence of coexisting Ca-rich and Ca-poor pyroxenes, a tholeiitic assemblage is indicated.Geochemical data confirm this prognosis and a continuous spread of compositions from basalt to tholeiitic andesite are interpreted in terms of fractional crystallisation. Modelling of the fractional crystallisation processes indicate an approach to cotectic conditions with fractionation at low pressures involving olivine, plagioclase, clinopyroxene and Ti-magnetite. Primitive magma compositions, indicated by low values of D.I. and 100 Mg/Mg + Fe²⁺ (atomic)>61, show low concentrations of the large ion lithophile elements such as Rb, Ba, Zr, Y, and K. The relatively high CaO content (>11 %) of these rocks invite comparison with high-calcium low-alkali tholeiitic liquids recognised in extrusive and intrusive magmas elsewhere in the North Atlantic Tertiary volcanic province and with magmas currently erupted at active spreading ridges.In north west Britain the field and stratigraphic distribution of these high-calcium low-alkali magmas suggests that they occupy a distinct chronological niche towards the top of the Palaeocene-Eocene volcanic succession succeeding eruption of mildly alkali and transitional basalts. As such, the refractory (high CaO, MgO, etc.) and large ion lithophile depleted geochemistry can be explained either by differential partial melting in the upper mantle source region or melting of a depleted and refractory mantle source which has already contributed to basalt genesis.     

Origin of metaluminous and alkaline volcanic rocks of the Latir volcanic field,northern Rio Grande rift,New Mexico

Volcanic rocks of the Latir volcanic field evolved in an open system by crystal fractionation, magma mixing, and crustal assimilation. Early high-SiO₂ rhyolites (28.5 Ma) fractionated from intermediate compositionmagmas that did not reach the surface. Most precaldera lavas have intermediate-compositions, from olivine basaltic-andesite (53% SiO₂) to quartz latite (67% SiO₂). The precaldera intermediate-composition lavas have anomalously high Ni and MgO contents and reversely zoned hornblende and augite phenocrysts, indicating mixing between primitive basalts and fractionated magmas. Isotopic data indicate that all of the intermediate-composition rocks studied contain large crustal components, although xenocrysts are found only in one unit. Inception of alkaline magmatism (alkalic dacite to high-SiO₂ peralkaline rhyolite) correlates with, initiation of regional extension approximately 26 Ma ago. The Questa caldera formed 26.5 Ma ago upon eruption of the >500 km³ high-SiO₂ peralkaline Amalia Tuff. Phenocryst compositions preserved in the cogenetic peralkaline granite suggest that the Amalia Tuff magma initially formed from a trace element-enriched, high-alkali metaluminous magma; isotopic data suggest that the parental magmas contain a large crustal component. Degassing of water- and halogen-rich alkali basalts may have provided sufficient volatile transport of alkalis and other elements into the overlying silicic magma chamber to drive the Amalia Tuff magma to peralkaline compositions. Trace element variations within the Amalia Tuff itself may be explained solely by 75% crystal fractionation of the observed phenocrysts. Crystal settling, however, is inconsistent with mineralogical variations in the tuff, and crystallization is thought to have occurred at a level below that tapped by the eruption. Spatially associated Miocene (15-11 Ma) lavas did not assimilate large amounts of crust or mix with primitive basaltic magmas. Both mixing and crustal assimilation processes appear to require development of relatively large magma chambers in the crust that are sustained by large basalt fluxes from the mantle. The lack of extensive crustal contamination and mixing in the Miocene lavas may be related to a decreased basalt flux or initiation of blockfaulting that prevented pooling of basaltic magma in the crust.     

Chemical composition of rock-forming minerals and crystallization physicochemical conditions of the Middle Eocene I-type Haji Abad pluton,SW Buin-Zahra,Iran

The Haji Abad intrusion is a well-exposed Middle Eocene I-type granodioritc pluton in the Urumieh–Dokhtar magmatic assemblage (UDMA). The major constituents of the investigated rocks are K-feldspar, quartz, plagioclase, pyroxene, and minor Fe–Ti oxide and hornblende. The plagioclase compositions fall in the labradorite, andesine, and oligoclase fields. The amphiboles range in composition from magnesio-hornblende to tremolite–hornblende of the calcic-amphibole group. Most pyroxenes principally plot in the field of diopside. The calculated average pressure of emplacement is 1.9 kbar for the granodioritic rocks, crystallizing at depths of about 6.7 km. The highest pressure estimated from clinopyroxene geobarometry (5 kbar) reflects initial pyroxene crystallization pressure, indicating initial crystallization depth (17.5 km) in the Haji Abad granodiorite. The estimated temperatures using two-feldspar thermometry give an average 724 °C. The calculated average temperature for clinopyroxene crystallization is 1090 °C. The pyroxene temperatures are higher than the estimated temperature by feldspar thermometry, indicating that the pyroxene and feldspar temperatures represent the first and late stages of magmatic crystallization of Haji Abad granodiorite, respectively. Most pyroxenes plot above the line of Fe³⁺?=?0, indicating they crystallized under relatively high oxygen fugacity or oxidized conditions. Furthermore, the results show that the Middle Eocene granitoids crystallized from magmas with H₂O content about 3.2 wt%. The relatively high water content is consistent with the generation environment of HAG rocks in an active continental margin and has allowed the magma to reach shallower crustal levels. The MMEs with ellipsoidal and spherical shapes show igneous microgranular textures and chilled margins, probably indicating the presence of magma mixing. Besides, core to rim compositional oscillations (An and FeO) for the plagioclase crystals serve as robust evidence to support magma mixing. The studied amphiboles and pyroxenes are grouped in the subalkaline fields that are consistent with crystallization from I-type calc-alkaine magma in the subduction environment related to active continental margin. Mineral chemistry data indicate that Haji Abad granodiorites were generated in an orogenic belt related to the volcanic arc setting consistent with the subduction of Neo-Tethyan oceanic crust beneath the central Iranian microcontinent.     

High-Magnesian Andesite Produced by Two-Stage Magma Mixing: a Case Study from Hachimantai, Northern Honshu, Japan

High-magnesian andesite occurs at Hachimantai, northern Honshu,Japan. Disequilibrium zoning features indicate that the phenocrystminerals were derived from three different magmas. Chemicalcompositions and zoning profiles are accounted for by two-stagemagma mixing: the first mixing occurred between a crystal-freebasalt magma and a more differentiated olivine basalt magma;the second stage occurred by mixing between the resultant ofthe first-stage mixing and a hypersthene–augite andesitemagma. Mass balance of phenocryst crystals shows that end-membercompositions were c. 52·0 wt % SiO₂ and 10·1 wt% MgO for the mafic end-member and 57·0 wt % SiO₂ forthe felsic end-member of the second-stage mixing. Phenocrystminerals of the first-stage mixing end-member indicate the similarityof the end-member composition to that of basalts from nearbyvolcanoes. The counterpart aphyric magma in the first-stagemixing was more magnesian than the estimated mafic end-member.Calculations of the phase equilibria of similar basalts fromnearby volcanoes and comparison of results with previous phaseequilibrium experiments showed that the olivine basalt end-memberof the first stage was hydrous and situated at a depth wherethe pressure was less than 2 kbar. Two-pyroxene thermometryestimates are about 1050°C for the pyroxenes derived fromthe felsic end-member of the second-stage mixing, and about1180°C for groundmass pyroxenes. Crystallization temperaturesof 1170–1230°C are estimated for minerals from themafic end-member of the second-stage mixing based on phase equilibriumcalculations. These similar temperature estimates between thegroundmass and the mafic end-member imply achievement of thermalequilibrium between end-members preceding crystallization. Themagma plumbing system of the eastern Hachimantai is illustratedby a recent volcanic event, involving lateral dike intrusiontoward a pressure source. The encounter of a laterally migratingbasalt dike and an andesite magma chamber triggered the magmamixing that produced the high-magnesian andesite. The modelcan account for the relation between the petrological modeland surface distribution of volcanic rocks. The infrequencyof such mixing-derived high-magnesian andesite stems from therarity of high-magnesian basalt as a potential mixing end-memberin northern Honshu. KEY WORDS: high-magnesian andesite; Hachimantai; Northern Honshu; high-magnesian basalt; two-stage magma mixing     

http://www.sciencedirect.com/science/article/pii/S1674987112001533

The collision of a divergent ocean ridge may evolve into two end cases:in the continuity of ocean-floor subduction.or in the detachment of the subducted plate.The northern Patagonia active plate margin has the unique situation that in Cenozoic time it has been subjected to two divergent ridge collisions,each one representing one of the end members.The Neogene Antarctica-Nazca divergent ridge collision evolved as a continuous ocean-floor subduction system,promoting a magmatic hiatus at the arc axis,the obduction of part of the ridge ocean-floor in the fore-arc.and basaltic volcanism in the back-arc.In contrast,the Paleogene Farallon-Aluk divergent ridge collision evolved into a transform margin,with the detachment and sinking of the Aluk plate and the development of a large slab window.As in the previous case,this collision promoted a magmatic hiatus at the arc axis,but the tectono-magmatic scenario changed to postorogenic synextensional volcanism that spread to the former fore-arc（basalt,andesite,rhyolite） and former back-arc（bimodal ignimbrite flare-up,basalt）.Geochemistry of this slab window synextensional volcanism shows more MORB-like basalts towards the former fore-arc,and MORB-OIB-like basalts towards the former back-arc.Instead,an isolated undeformable crustal block in the former back-arc,with an "epeirogenic" response to the slab window and extensional regime,was covered by OIB-type basalts after uplift.Major elements show that slab window basalts reach TiCh values up to 3 wt%,as compared with the top value of 1.5 wt%of arc magmas.Besides,the MgO with respect to（FeO^t + Al₂O₃） ratio helps to distinguish slab window magma changes from the former fore-arc to the former back-arc and also with respect to the "epeirogenic" block.Higher contents of HFS elements such as Nb and Ta also help to distinguish this slab window from arc magmas and also,to distinguish slab window magma changes from the former fore-arc to the former back-arc and "epeirogenic" block settings.The isotope compositions of slab window magmatism show a disparate coeval array from MORB to crustal sources,interpreted as a consequence of the lack of protracted storage and homogenization due to the extensional setting.     

新疆准噶尔北缘北塔山组火山岩年龄及岩石成因

对准噶尔北缘北塔山组辉石玄武岩进行了LA-ICP-MS锆石U-Pb 年龄测定, 获得了玄武岩的喷发年龄380.5±2.2Ma,表明北塔山组火山岩形成于中泥盆世。该地层火山岩中辉石玄武岩和无斑玄武岩的SiO₂含量为47.55%~52.97%、Al₂O₃的含量为8.44%~20.00%、TiO₂为0.5%~1.2%,MgO含量为2.8%~15.35%、CaO为3.98%~14.83%、FeO^T为9.46%~19.23%,具有亚碱性拉斑玄武岩的特征。其微量元素显示富集大离子亲石元素(LILE)和轻稀土元素(LREE),亏损Nb、Ta和Ti,Eu异常不明显。它们具有极低的初始⁸⁷Sr/⁸⁶Sr同位素比值(0.703835~0.704337)和高的ε_Nd(381Ma)值(+6.84~+12.3,t=381Ma)的亏损地幔源区特征。结合区域地质背景,北塔山组火山岩形成于与俯冲作用相关的构造环境,是准噶尔古洋盆于泥盆世时发生的俯冲-消减所引发的岛弧岩浆作用的地质记录。岩浆源区为被流体或沉积物熔体交代改造的地幔楔和软流圈地幔,不同类型的岩石系不同成分的原始岩浆经不同演化过程的产物。     

Geochemical and mineralogical evidence for the occurrence of at least three distinct magma types in the ‘famous’ region

Bulk rock major and trace element variations in selected basalts from the Famous area, in conjunction with a detailed study of the chemical compositions of phenocryst minerals and associated melt inclusions are used to place constraints on the genetic relationship among the various lava types. The distribution of NiO in olivine and Cr-spinel phenocrysts distinguishes the picritic basalts, plagioclase phyric basalts and plagioclase-pyroxene basalts from the olivine basalts. For a given Mg/Mg+Fe²⁺ atomic ratio of the mineral, the NiO content of these phenocrysts in the former three basalt types is low relative to that in the phenocrysts in the olivine basalts. The Zr/Nb ratio of the lavas similarly distinguishes the olivine basalts from the plagioclase phyric and plagioclase pyroxene basalts and, in addition, distinguishes the picritic basalts from the other basalt types. These differences indicate that the different magma groups could not have been processed through the same magma chamber, and preclude any direct inter-relationship via open or closed system fractional crystallization.The Fe-Mg partitioning between olivine and host rock suggests that the picritic basalts represent olivine (±Cr-spinel) enriched magmas, derived from a less MgO rich parental magma. The partitioning of Fe and Mg between olivine, Cr-spinel and coexisting liquid is used to predict a primary magma composition parental to the picritic basalts. This magma is characterized by relatively high MgO (12.3%) and CaO (12.6%) and low FeO^* (7.96%) and TiO₂ (0.63%).Least squares calculations indicate that the plagioclase phyric basalts are related to the plagioclase-pyroxene basalts by plagioclase and minor clinopyroxene and olivine accumulation. The compositional variations within the olivine basalts can be accounted for by fractionation of plagioclase, clinopyroxene and olivine in an open system, steady state, magma chamber in the average proportions 453223. It is suggested that the most primitive olivine basalts can be derived from a pristine mantle composition by approximately 17% equilibrium partial melting. Although distinguished by its higher Zr/Nb ratio and lower NiO content of phenocryst phases, the magma parental to the picritic basalts can be derived from a similar source composition by approximately 27% equilibrium partial melting. It is suggested that the parental magma to the plagioclase-pyroxene and plagioclase phyric basalts might have been derived from greater depth resulting in the fractionation of the Zr/Nb ratio by equilibration with residual garnet.C.O.B. Contribution No. 722     

Ultramafic and Mafic Inclusions from Adak Island: Crystallization History, and Implications for the Nature of Primary Magmas and Crustal Evolution in the Aleutian Arc

Xenolithic inclusions in calc-alkaline andesite from Mt. Moffettvolcano, Adak Island, Aleutian arc, reveal a nearly continuousrecord of crystallization of basaltic magmas in the crust, andpossibly upper mantle, of the arc. The record is more detailedand continuous than that obtained from study of calc-alkalinevolcanic rocks in the arc. Cumulate xenoliths form a progressiveseries in modal mineralogy from ultramafic, hornblende-bearingolivine clinopyroxenite to both hornblende-bearing and hornblende-freegabbros. The cumulate hornblende gabbro xenoliths are typicalof those found in island arc andesites worldwide. Xenolithicinclusions without cumulate textures, here termed compositexenoliths, are characterized by forsteritic olivine, zoned Cr-diopsideand hornblende, and are interpreted to have resulted from reactionand chilling upon magma mixing at depth. The olivine and clinopyroxene in both cumulate and compositexenoliths show the largest and the most complete variation trendsfor Ni, Cr, and FeO/MgO ratio yet reported in igneous xenolithsfrom island arc volcanic rocks. Variation of Ni in olivine indicatesthat the parent magmas for the xenoliths had minimum MgO contentsof 9 wt. per cent. Variation of Cr in clinopyroxene indicatesthat the magmas were basaltic rather than picritic, probablyin equilibrium with spinel lherzolite at near Moho depths. Successiveinjections of batches of primary melt into a magma chamber fractionatingolivine and clinopyroxene can reproduce observed compatibleelement depletion trends. A steady-state process of cotecticcrystallization in a magma chamber continually replenished withbasaltic magma is a possible mechanism for producing large accumulationsof olivine and clinopyroxene, suggesting that Alaskan-type ultramaficcomplexes are related to hydrous basaltic magmas in island arcs.This steady-state open-system crystallization process can alsoyield the abundant high-alumina basalt type in the Aleutianarc. Continued crystallization of high-alumina basalt in lowercrustal magma chambers, recorded in a mineralogically coherentseries of pyroxenite to hornblende gabbro xenoliths, can yieldbasaltic to andesitic magmas of the calc-alkaline series. No xenoliths with a sedimentary protolith have been found atMt Moffett, evidence that the arc crust is igneous in origin,with the lower crust formed of gabbro crystallized from mantle-derivedmelts. Ultramafic cumulates may reside in both the lower crustor upper mantle beneath the arc. A model is proposed wherebythe cumulate crystallization products of hydrous, mantle beneaththe arc. A model is define the upper mantle and lower crustof the arc over time.The net composition added to the crustof the arc is that of high-alumina basalt.