Library

Notes: Twenty five elements in twenty six geochemical reference standards analyzed by X-ray fluorescence spectrometry yield major and trace element concentrations close to consensus values. Ninety percent of our analyses agree with consensus values for standards to within pm 0.5 to 1.5 relative percent for major elements and pm 3 to 5 relative percent or pm 1-3 ppm, whichever is higher, for trace elements. Consistent divergences from consensus values of trace elements are noted.

Notes: Abstract Available geochemical and field data suggest that three different periods of igneous activity have occurred on Viti Levu. Rocks of the first period are “island arc tholeiites”; of the second, a calc-alkaline series; and of the third, shoshonites. Each period has a geochemical distinctiveness. The temporal sequence also corresponds to a spatial zonation analogous to that observed in many currently active island arcs. K2O and the larger trace elements increase south to north and with time, whereas iron enrichment and Na2O/K2O ratios decrease. Initial Sr 87/86 ratios average about 0.7041 in rocks of all periods. If Viti Levu magmas were genetically related to underthrust oceanic crust, as is argued for comparable ones of modern island arcs, then the island must have drifted or been rotated to its present position within the last 5–10 m.y.

Notes: Abstract A test of the proposition that calc-alkaline magmas are direct partial melts of underthrust oceanic crust is presented. It involves numerical evaluations of whether or not the major and trace element and isotopic composition of a Fijian calc-alkaline rock suite is consistent with these rocks representing unfractionated partial melts of oceanic crust at high pressures. Experimental data for one of the samples constrain the calculations. When compositions of liquidus minerals at 27 kb are combined with compositions of the volcanic rocks, close approximations can be made to the composition of oceanic crust only if the degree of partial melting is between ∼20% (dacite) and ∼45% (basaltic-andesite), and if accessory minerals are refractory phases. Concentrations of elements such as K, Rb, Sr, Pb, Th, and U, and 87Sr/86Sr ratios in the Fijian suite can be satisfactorily explained only if the parental material consisted of altered rather than fresh ocean floor basalt. Sediments are not likely to have been involved. Concentrations of Na, Ni, Co, Cr, Sc, V, the REE, Y, Zr, Hf, and Nb cannot be explained unless, or in some cases even if, several accessory phases are partially refractory. Therefore, partial melting of underthrust lithosphere does not seem likely to produce magmas with the composition of at least one quite typical calc-alkaline suite.

Notes: Abstract Arenal volcano in Costa Rica has been erupting nearly continuously, but at a diminishing rate, since 1968, producing approximately 0.35 km3 of lavas and tephras that have shown consistent variations in chemistry and mineralogy. From the beginning of the eruption in July 1968 to early 1970 (stage 1, vol.=0.12 km3) tephras and lavas became richer in Ca, Mg, Ni, Cr, Fe, Ti, V, and Sc and poorer in Al2O3 and SiO2. Concentrations of incompatible trace elements (including Sr) decreased by 5%–20%. Phenocryst contents increased 20–50 vol%. During stage 2 (1970–1973, vol. = 0.13 km3) concentrations of compatible trace elements rose, and concentrations of incompatible trace elements either remained constant or also rose. Al2O3 contents decreased by 1 wt%. Phenocryst content increased slightly, principally due to increased orthopyroxene. During stage 3 (mid-1974 to the present, vol.= 0.10 km3) concentrations of SiO2 increased by 1 wt%, compatible trace elements decreased slightly, and incompatible trace element concentrations increased by 5% to 10%. Although crystals increased in size during stage 3, their overall abundance stayed roughly constant. Our modeling suggests that early stage-1 magmas were produced by boundary layer fractionation under high-p H2O conditions of an unseen basaltic andesitic magma that intruded into the Arenal system after approximately 500 B.P. Changes in composition during stage 2 resulted from mixing of this more mafic original magma with new magma that had a similar SiO2 content, but higher compatible and incompatible element concentrations. The changes during stage 3 resulted from continued influx of the same magma plus crystal removal. We conclude that the eruption proceeded in the following way. Before 1968 zoned stage-1 magma resided in the deep crust below Arenal. A new magma intruded into this chamber in July 1968 causing ejection of the stage-1 magmas. The intruding magma mixed with mafic portions of the original chamber producing the mixed lavas of stage 2. Continued mixing plus crystal fractionation along the chamber and conduit walls produced stage-3 lavas. The time scales of crustal level magmatic processes at Arenal range 100–103 years, which are 3–6 orders of magnitude shorter than those of larger, more silicic systems.