Analytical data for Sr, Rb, Cs, Ba, Pb, rare earth elements, Y, Th, U, Zr, Hf, Sn, Nb, Mo, Ni, Co, V, Cr, Sc, Cu and major elements are reported for eocene volcanic rocks cropping out in the Kastamonu area, Pontic chain of Northern Turkey. SiO2% versus K2O% relationship shows that the analyzed samples belong to two major groups: the basaltic andesitic and the andesitic ones. High-K basaltic andesites and low-K andesites occur too. Although emplaced on continental type basement (the North Anatolian Crystalline Swell), the Pontic eocene volcanics show elemental abundances closely comparable with typical island arc calc-alkaline suites, e.g. low SiO2% range, low to moderate K2O% and large cations (Cs, Rb, Sr, Ba, Pb) contents and REE patterns with fractionated light and almost flat heavy REE patterns. ΣREE and highly charged cations (Th, U, Hf, Sn, Zr) are slightly higher than typical calc-alkaline values. Ferromagnesian elements show variable values. Within the basaltic andesite group the increase of K%, large cations, ΣREE, La/Yb ratio and high valency cations and the decrease of ferromagnesian element abundances with increasing SiO2% content indicate that the rock types making up this group developed by crystalliquid fractionation of olivine and clinopyroxene from a basic parent magma. Trace element concentration suggest that the andesite group was not derived by crystal-liquid fractionation processes from the basaltic andesites, but could represent a distinct group of rocks derived from a different parent magma.

Geochemistry of eocene calc-alkaline volcanic rocks from the Kastamonu area, Northern Turkey

Data from experimental runs, coexisting phases in ultramafic rocks and phenocryst-matrix pairs in volcanic rocks have been used to compile a table of mineral-liquid distribution coefficients for Ti, Zr, Y, and Nb for basic, intermediate and acid melt compositions. These values have then been used to interpret variations of these elements, first in basalts and second, during fractional crystallization from basic to acid magmas. For basalts, petrogenetic modelling of Zr/Y, Zr/Ti, and Zr/Nb ratios, when used in conjunction with REE, Cr and isotopic variations, suggests that: (1) the increase in Zr/Y ratio from mid-ocean ridge to within plate basalts and the low Zr/Nb ratios of alkalic basalts are due to (fluid controlled) source heterogeneities; (2) the low Zr and Zr/Y ratio of volcanic arc basalts results from high degree of partial melting of a depleted source; and (3) the high Zr and similar Zr/Y ratio of basalts from fast spreading relative to slow spreading ridges results from open-system fractional crystallization. Modelling of fractionation trends in more evolved rocks using Y-Zr, Ti-Zr and Nb-Zr diagrams highlights in particular the change in crystallizing mafic phases from island arcs (clinopyroxene-dominated) to Andean-type arcs (amphibole±biotite-dominated). These methods can be applied to altered lavas of unknown affinities to provide additional information on their genesis and eruptive environment.

Petrogenetic implications of Ti, Zr, Y, and Nb variations in volcanic rocks

Zircon chemistry and magma mixing, SE China: In-situ analysis of Hf isotopes, Tonglu and Pingtan igneous complexes

Amphibole thermodynamics are approximated with the symmetric formalism (regular solution model for within-site non-ideality and a reciprocal solution model for cross-site-terms) in order to formulate improved thermometers for amphibole-plagioclase assemblages. This approximation provides a convenient framework with which to account for composition-dependence of the ideal (mixing-on-sites) equilibrium constants for the equilibria:
 For A and B all possible within-site and cross-site interactions among the species □−K−Na−Ca−Mg−Fe2+−Fe3+−Al−Si on the A, M4, M1, M3, M2 and T1 amphibole crystallographic sites were examined. Of the 36 possible interaction energy terms, application of the symmetric formalism results in a dramatic simplification to eight independent parameters. Plagioclase nonideality is modelled using Darken's quadratic formalism. We have supplemented an experimental data set of 92 amphibole-plagioclase pairs with 215 natural pairs from igneous and metamorphic rocks in which the pressure and temperature of equilibration are well constrained. Regression of the combined dataset yields values for the eight interaction parameters as well as for apparent enthalpy, entropy and volume changes for each reaction. These parameters are used to formulate two new thermometers, which perform well (±40°C) in the range 400–1000°C and 1–15 kbar over a broad range of bulk compositions, including tschermakitic amphiboles from garnet amphibolites which caused problems for the simple thermometer of Blundy and Holland (1990). For silica-saturated rocks both thermometers may be applied: in silica-undersaturated rocks or magmas thermometer B alone can be applied. An improved procedure for estimation of ferric iron in calcic amphiboles is presented in the appendix.

Non-ideal interactions in calcic amphiboles and their bearing on amphibole-plagioclase thermometry

Fifteen andesite-dacite stratovolcanoes on the volcanic front of a single segment of the Andean arc show along-arc changes in isotopic and elemental ratios that demonstrate large crustal contributions to magma genesis. All 15 centers lie 90 km above the Benioff zone and 280±20 km from the trench axis. Rate and geometry of subduction and composition and age of subducted sediments and seafloor are nearly constant along the segment. Nonetheless, from S to N along the volcanic front (at 57.5% SiO2) K2O rises from 1.1 to 2.4 wt %, Ba from 300 to 600 ppm, and Ce from 25 to 50 ppm, whereas FeO*/MgO declines from >2.5 to 1.4. Ce/Yb and Hf/Lu triple northward, in part reflecting suppression of HREE enrichment by deep-crustal garnet. Rb, Cs, Th, and U contents all rise markedly from S to N, but Rb/Cs values double northward — opposite to prediction were the regional alkali enrichment controlled by sediment subduction. K/Rb drops steeply and scatters greatly within many (biotite-free) andesitic suites. Wide diversity in Zr/Hf, Zr/Rb, Ba/Ta, and Ba/La within and among neighboring suites (which lack zircon and alkali feldspar) largely reflects local variability of intracrustal (not slab or mantle) contributions. Pb-isotope data define a limited range that straddles the Stacey-Kramers line, is bracketed by values of local basement rocks, in part plots above the field of Nazca plate sediment, and shows no indication of a steep (mantle+sedimentary) Pb mixing trend. 87Sr/86Sr values rise northward from 0.7036 to 0.7057, and 143Nd/144Nd values drop from 0.5129 to 0.5125. A northward climb in basal elevation of volcanic-front edifices from 1350 m to 4500 m elevation coincides with a Bougueranomaly gradient from −95 to −295 mgal, interpreted to indicate thickening of the crust from 30–35 km to 50–60 km. Complementary to the thickening crust, the mantle wedge beneath the front thins northward from about 60 km to 30–40 km (as slab depth is constant). The thick northern crust contains an abundance of Paleozoic and Triassic rocks, whereas the proportion of younger arc-intrusive basement increases southward. Primitive basalts are unknown anywhere along the arc. Base-level isotopic and chemical values for each volcano are established by blending of subcrustal and deep-crustal magmas in zones of melting, assimilation, storage and homogenization (MASH) at the mantle-crust transition. Scavenging of mid-to upper-crustal silicic-alkalic melts and intracrustal AFC (prominent at the largest center) can subsequently modify ascending magmas, but the base-level geochemical signature at each center reflects the depth of its MASH zone and the age, composition, and proportional contribution of the lowermost crust.

Crustal contributions to arc magmatism in the Andes of Central Chile

Experimental crystallization of olivine tholeiite and $$SiO_{2}$$-saturated tholeiite compositions has demonstrated that addition of water up to the limit of solubility markedly increases the maximum pressure of olivine stability. At depths within the upper mantle from which picritic magmas originate under dry conditions, water-saturated partial melting of peridotite can produce $$SiO_{2}$$-saturated tholeiite liquids. Unless they segregate from residual mantle at very shallow depths, magmas of this type with water contents >5% must fractionate at least olivine during ascent to the earth's surface, thus yielding quartz tholeiites or basaltic andesites. The geochemistry of basalts and basaltic andesites of the island-arc tholeiitic series is compatible with origin involving olivine fractionation from primitive olivine-poor tholeiite magmas. The sites of initiation of partial melting and segregation of these magmas from peridotite mantle will be controlled by availability of water from dehydration of downgo...

Effect of Water on Olivine Stability in Tholeiites and the Production of Silica-Saturated Magmas in the Island-Arc Environment

Water-Saturated and -Undersaturated Melting of Metaluminous and Peraluminous Crustal Compositions at 10 kb: Evidence for the Origin of Silicic Magmas in the Taupo Volcanic Zone, New Zealand, and Other Occurrences

Monogenetic volcanoes have long been regarded as simple in nature, involving single magma batches and uncomplicated evolutions; however, recent detailed research into individual centres is challenging that assumption. Mt Rouse (Kolor) is the volumetrically largest volcano in the monogenetic Newer Volcanics Province of southeast Australia. This study presents new major, trace and Sr–Nd–Pb isotope data for samples selected on the basis of a detailed stratigraphic framework analysis of the volcanic products from Mt Rouse. The volcano is the product of three magma batches geochemically similar to Ocean–Island basalts, featuring increasing LREE enrichment with each magma batch (batches A, B and C) but no evidence of crustal contamination; the Sr–Nd–Pb isotopes define two groupings. Modelling suggests that the magmas were sourced from a zone of partial melting crossing the lithosphere–asthenosphere boundary, with batch A forming a large-volume partial melt in the deep lithosphere (1.7 GPa/55.5 km); and batches B and C from similar areas within the shallow asthenosphere (1.88 GPa/61 km and 1.94 GPa/63 km, respectively). The formation and extraction of these magmas may have been due to high deformation rates in the mantle caused by edge-driven convection and asthenospheric upwelling. The lithosphere–asthenosphere boundary is important with respect to NVP volcanism. An eruption chronology involves sequential eruption of magma batches A, C and B, followed by simultaneous eruption of batches A and B. Mt Rouse is a complex polymagmatic monogenetic volcano that illustrates the complexity of monogenetic volcanism and demonstrates the importance of combining detailed stratigraphic analysis alongside systematic geochemical sampling.

Variation in parental magmas of Mt Rouse, a complex polymagmatic monogenetic volcano in the basaltic intraplate Newer Volcanics Province, southeast Australia

Experimental rare earth element partition coefficients for garnet, clinopyroxene and amphibole coexisting with andesitic and basaltic liquids

Since Mesozoic time, Java and Bali have formed part of an evolving system of island arcs comprising the Sunda arc of Indonesia. The present tectonic setting is relatively simple with subduction occurring at the Java Trench to the south. A north-dipping Benioff seismic zone delineates an underthrust lithospheric slab to depths of approximately 600 km beneath the Java Sea. Quaternary lavas of the ‘normal island arc association’ range from tholeiites to high-K calc-alkaline lavas over Benioff zone depths from 120–250 km, respectively. More abundant calc-alkaline lavas lie between these extremes. High-K alkaline lavas are found over Benioff zone depths in excess of 300 km.

Ian A Nicholls

Papers

Effect of Water on Olivine Stability in Tholeiites and the Production of Silica-Saturated Magmas in the Island-Arc Environment

Water-Saturated and -Undersaturated Melting of Metaluminous and Peraluminous Crustal Compositions at 10 kb: Evidence for the Origin of Silicic Magmas in the Taupo Volcanic Zone, New Zealand, and Other Occurrences

Variation in parental magmas of Mt Rouse, a complex polymagmatic monogenetic volcano in the basaltic intraplate Newer Volcanics Province, southeast Australia

Experimental rare earth element partition coefficients for garnet, clinopyroxene and amphibole coexisting with andesitic and basaltic liquids

Spatial variations in the geochemistry of quaternary lavas across the Sunda arc in Java and Bali