ALBERT

Notes: The USGS reference glasses GSA-1G, GSC-1G, GSD-1G, GSE-1G, BCR-2G, BHVO-2G and BIR-1G were investigated by different analytical techniques. All these materials have a geological (basaltic) matrix and are therefore useful in igneous geochemistry as matrix-matched reference materials for microanalytical techniques. The new GS glasses have trace elements in groups at concentration levels of about 〈 0.01, 5, 50 and 500 μg g-1. Their major element compositions have been determined by EPMA, and trace elements have been analysed by LA-ICP-MS and two isotope dilution techniques using TIMS and ICP-MS. EPMA and LA-ICP-MS analyses indicated that the USGS reference glasses are homogeneous at the μm to mm scale with respect to major (variations 〈 1-2%) and most trace elements (variations 1-4%). Trace element data obtained from the different analytical techniques agreed within an uncertainty of 1-5%, indicating that between method results are comparable. Therefore, the preliminary working values for the four USGS GS glasses calculated from these data have a low level of uncertainty.

Notes: Abstract We present new isotopic data for Sr and Nd in basalts and alkalic volcanics from Kohala volcano, Hawaii, which had previously been described by Feigenson et al. (1983). These data complement our own isotopic data presented in that paper and those given in the companion paper by Lanphere and Frey (1986). We show that in spite of appearances to the contrary, there is no significant analytical bias in our previously published analyses. Accidental sampling bias and one erroneous value prevented us from recognizing the isotopic heterogeneity in our previously published data. The new data both confirm the Sr-isotopic distinction between Pololu and Hawi volcanics discovered by Lanphere and Frey and narrow the gap between them significantly. The two data sets agree for the Hawi samples, but the mean 87Sr/86Sr=0.703651±13 for our Pololu basalts is significantly lower than the mean 87Sr/86Sr= 0.703748±18 found by Lanphere and Frey. The Ndisotopic ratios are also heterogeneous, but they overlap for the two formations. We agree with the assessment of Lanphere and Frey that some of our samples originally classified as belonging to the Hawi Formation are actually derived from the uppermost Pololu Formation, but with some stratigraphic ambiguities remaining. We believe that our previous results of inverse modelling are valid for the tholeiitic and moderately alkalic Pololu Formation despite the isotopic heterogeneity because this heterogeneity does not correlate with the trace element chemistry of the Pololu samples. The severe depletion of Sc, which correlates with decreasing CaO/Al2O3 ratios and increasing Yb concentrations, confirms the importance of clinopyroxene fractionation in the evolved lavas of the Hawi Formation. In addition, apatite precipitation did fractionate the P/Ce ratios in the more evolved Hawi lavas, but its effect on the REE abundances is still uncertain and may not be significant. The MgO — P2O5 plot of Lanphere and Frey does not provide compelling evidence against a simple genetic relationship between Pololu and Hawi lavas. The internal consistency of the (fractionation corrected) trace element ratios such as Ba/Ce indicates that Ba is depleted in both the Hawi and the Pololu sources and that these sources do have similar chemistry. Finally, we show that contrary to the conclusions of Lanphere and Frey the REE patterns of Kohala volcanics can be generated from sources with only slightly negatively sloping REE patterns without involvement of garnet, as was indicated by the formal inversion analysis. Models which include garnet yield more highly anomalous source abundance patterns and calculated bulk-source partition coefficients which are inconsistent with the presence of garnet. The persistence of residual garnet is also inconsistent with the absence of significant heavy-REE fractionation among the Pololu basalts.

Notes: Abstract From the quartz porphyry occurrences of Haigerach and Geisberg (Central Schwarzwald), which were dated by minerals and whole-rock samples, the whole-rock samples generally yielded lower ages than the minerals. This result agrees with other studies on apparently rejuvinated whole-rock ages of acid volcanic rocks (compare McKerrow et al. 1980). Petrographic and geochemical observations show that two processes disturbed the Rb-Sr relations: 1) fast alterations immediately after extrusion, such as sericitization during autohydrothermal bleaching in the pipe area of the volcanoes, gain of Rb, addition of common Sr. 2) loss of radiogenic 87Sr due to long-lasting exchange processes with groundwaters. The combined result of the two processes is a kind of isochron rotation simulating younger whole-rock ages and higher initial Sr isotope ratios. Our results on the two quartz porphyries indicate that whole-rock dating of such acid volcanics is not succesful.

Notes: Abstract Rb-Sr mineral ages and Sr isotopic ratios were determined for several Permian rhyolites of the Schwarzwald, mainly by using mica-apatite pairs. Extrusion ages between_307+5 and 286+7 Ma were found (λ Rb=1.42· 10−11 a−1, 2σ). The initial Sr isotopic ratios range from 0,710 to 0.7125, with one exception (St. Märgen: 0.706). The Rb-Sr age of the granite porphyry Schweighof in the Southern Schwarzwald is 323+4 Ma. Thus the subsequent volcanic activity of the Hercynian orogeny lasted nearly 20–30 Ma, starting in the Late Carboniferous and culminating in the Early Permian. The volcanic activity moved in time from South to North. In the Southern as well as the Northern Schwarzwald a hiatus of about 20 Ma exists between late orogenic plutonism and subsequent volcanism. The initial ratios lie on the crustal evolution line of Schwarzwald basement and favour, with the St. Märgen porphyry as exception, a crustal provenance of the volcanic magmas.

Notes: Abstract During the Mauna Ulu flank eruption on Kilauea, Hawaii, the concentrations in the lavas of the minor elements K, P, Na and Ti, and the incompatible trace elements (analyzed by isotope dilution) K, Rb, Cs, Ba, Sr, and the REE (except Yb) decreased monotonically and linearly with the time (or date) of the eruption. At the same time, the concentrations of the major elements and of Yb, and the ratios of K/Rb, K/Cs, Ba/Rb, 87Sr/86Sr and 143Nd/144Nd remained constant. Most of the scatter in the raw concentration data is removed by a simple correction for olivine (plus chromite) fractionation previously established by Wright et al. (1975). These results are explained by simple equilibrium partial melting of a uniform source. The degree of melting increased by about 20% of the initial value during the course of the eruption. The trace element data are inverted by the method originated by Minster and Allègre (1978) and simplified by Hofmann and Feigenson (1983). The source has the following element (or isotope) ratios: K/Rb=501±7, Ba/Rb=14.0±0.5, Rb/Cs=95±7, Rb/Sr=0.0193 (+0.0045, −0.0090), (Ce/Ba)CN= 1.1±0.1, (Sr/Ba)CN=1.19 (+0.30, −0.19), 87Sr/86Sr=0.703521±0.000016, and 143Nd/144Nd=0.512966±0.000008. The REE pattern of the source has a nearly flat or slightly negative slope (=relative LREE enrichment) between Ce and Dy and a strongly positive slope between Dy and Yb. However, this relative HREE enrichment is poorly constrained by the analytical data, is highly model dependent and may not be a true source feature. The Yb concentration in the source is particularly poorly constrained because it is essentially constant in the melts. On the other hand, this special feature demonstrates that Yb must be buffered by a mineral phase with a high partition coefficient for Yb, namely garnet. The calculated clinopyroxene/garnet ratio in the source is roughly equal to one. In contrast, the source of Kohala volcano had previously been found to contain little or no garnet.

Notes: Abstract In the Central Dinaric Ophiolite Belt (CDOB) peridotites and associated metamorphic rocks of various grades tectonically overlie an olistostrome melange of middle to late Jurassic age. Peridotites and underlying slices of mafic granulites (partially transformed to gamet amphibolites) are intruded by doleritic dikes which do not occur in the melange. The melange contains blocks of subgreywackes and cherts as well as those of pillow lavas and massive diabase (spilites). CDOB peridotites are in the spinel peridotite facies, but locally spinel-plagioclase peridotites occur as well. All peridotites have lherzolitic compositions showing several significant element correlations: Al2O3, CaO, TiO2, Na2O and Cu are negatively correlated and Ni is positively correlated with MgO. Recent estimates of primitive mantle compositions lie near the low-MgO end point of each correlation trend. Al/Ti and Ca/Al ratios of CDOB lherzolites are for the most part higher than the range observed in chondrites. However, when a few samples with extreme compositions are excluded, Al/Ti and Ca/Al are positively correlated with MgO, and the samples at the low-MgO end have near-chondritic Ca/Al but slightly higher than chondritic Al/Ti ratios. Chondrite-normalized REE patterns of CDOB lherzolites show extreme depletions in LREE providing strong evidence for the absence of any metasomatic renrichment. The lack of correlation between highly incompatible elements (LREE) and moderately incompatible elements (HREE, Ti, Na, Al, Ca) together with the extremely low La/Sm ratios suggest that fractional or very small increment melt removal played a role in the genesis of these lherzolites. Four out of five lherzolites yield and apparent Sm-Nd isochron age of 136±15 Ma with an ɛNb of 6.0±1.1 (bulk rocks and clinopyroxene separates). One sample has an exceptionally high ɛNd of about 23. The mafic igneous rocks scatter around the lower end of the 136 Ma reference isochron allowing, but not proving, a genetic relationship with a mantle having a Nd isotopic composition which is similar to that of CDOB lherzolites. LIL element abundances of spilites and doleritic dike rocks suggest some hydrothermal alteration. In primitive mantle-normalized concentration diagrams none of these mafic igneous rocks shows a significant negative Nb-Ta anomaly. Chondrite-normalized REE patterns of both rock types are essentially flat. Whereas the inferred primary compositions of the spilites compare well with those of E-type MORBs, the doleritic dike rocks show elemental ratios similar to those normally found in back-arc basin tholeiites.