Hirokazu Fujimaki

JNdi-1 : a neodymium isotopic reference in consistency with LaJolla neodymium

Abstract A neodymium oxide with relative 143Nd/144Nd ratio 1.000503±1(1 σm) to LaJolla Nd was prepared as a new isotopic reference. The neodymium reagent was selected from two points of view as follows. The first is low abundance of neighboring elements Ce and Sm, which affects isobaric interference. The second is high 143Nd/144Nd ratio, which is closer to those of chondritic and mantle-derived materials. The 143Nd/144Nd ratio of the reagent was measured alternately with LaJolla Nd to get a coherency with LaJolla Nd using 12 mass spectrometers in 11 laboratories in Japan. Aliquots of this neodymium oxide reagent named JNdi-1 are available upon request from the Geological Survey of Japan and may be useful for precise interlaboratory calibration of Nd isotopes.

Exsolved garnet-bearing pyroxene megacrysts from some South African kimberlites

Clinopyroxene and orthopyroxene megacrysts containing garnet lamellae up to 1.2 mm thick as an exsolved phase are found rarely in kimberlites from Frank Smith and Bellsbank. Chemically the clinopyroxenes are characteristically subcalcic, being within the range of 100 Ca/Ca + Mg + Fe = 27 to 36, and the orthopyroxenes are characterized by high Al2O3 and Cr2O3. Immediately after crystallization during very slow cooling, clinopyroxene and orthopyroxene exsolve wide-spaced orthopyroxene and clinopyroxene phases parallel to (100) of the host phases, respectively, then both host and exsolved phases exsolve garnet lamellae. Topotactic relations between pyroxenes and garnet are determined by X-ray for the first time. Partitioning of major and minor elements among the coexisting clinopyroxene, orthopyroxene and garnet in pyroxene megacrysts is the same as that of the granular-type garnet peridotite xenoliths in Lesotho and South African kimberlies. Mineralogy and chemistry indicate that subcalcic clinopyroxene and orthopyroxene megacrysts contain respectively about 10 and 3 mole % of the garnet molecule in solid solution.

Fractional crystallization of the basaltic suite of Usu volcano, southwest Hokkaido, Japan, and its relationships with the associated felsic suite

Abstract REE concentrations were determined for four basalts, two basaltic andesites, three dacites and one rhyolite from Usu volcano, SW Hokkaido, Japan, and are reported with their mineralogical data. The basic rocks are tholeiitic, whereas the felsic rocks are calc-alkaline. No intermediate andesite has been erupted. The REE abundances of the basic rocks increase with increasing FeO ∗ MgO ratios and the mineral compositions are consistent with low-pressure fractionation. The variation of the REE concentrations can also be explained by low-pressure fractionation. In contrast, the chemical features of the felsic rocks can be hardly accounted for by low- or high-pressure fractionation; the felsic rocks are more depleted in HREE than the most differentiated basaltic andesite. A model calculation is suggestive of their origin: the felsic rocks can be produced by remelting of an intrusive body of tholeiitic basic magma.

REE abundances in exsolved garnet-bearing clinopyroxene megacryst from Bellsbank kimberlite (South Africa)

Abstract REE abundances of subcalcic clinopyroxene megacryst and its exsolved phases have been determined by mass spectrometry. The megacryst is characterized by rare-earth element (REE) concentrations higher than chondrite by a factor of 1.5 to 2.4 and a rather flat chondrite-normalized pattern. REE data indicate that the clinopyroxene megacryst is in equilibrium with an alkali picrite magma, but not with a kimberlite. Partitioning of major elements among coexisting diopside, enstatite and garnet, which have exsolved from the megacryst, is the same as that of the granular-type garnet peridotite xenoliths, whereas partitioning of REE among the phases is rather similar to the sheared peridotites. The data indicate that chemical equilibrium of major elements and REE was not maintained among the exsolved phases during exsolution and subsequent recrystallization, after the formation of the original homogeneous clinopyroxene megacryst.

Plutonic inclusions and olivines in high-K volcanics from Ulreung island, Korea

SummaryMajor and trace element data are presented for four alkali gabbroic inclusions, two monzonitic inclusions, and nine syenitic inclusions from Ulreung island, Korea. Analytical results are also given for the mineral constituents. Although the major element chemistry suggests that the plutonic inclusions are comagmatic with the associated volcanic rocks, the trace element data demonstrate that they do not represent a simple liquid line of descent. In addition, the mineralogical data indicate that they are not likely to represent cumulates on the floor of the magma chamber from which the observed volcanic rocks have been derived. Titanbiotite crystallization preceded kaersutite crystallization in the plutonic rocks but that order was inverse in the volcanic rocks. The trachytic-phonolitic rocks contain Fe-rich olivine phenocrysts, whereas the plutonic inclusions do not. These discrepancies can be accounted for by the assumption that the investigated plutonic rocks represent some cumulus parts of intrusive bodies solidified at shallower depth than the magma reservoir beneath the island. Petrographic features of the gabbroic inclusions are suggestive that olivine was probably in a reaction relationship with liquid to form titanbiotite. Comparison with petrological data of the volcanic rocks also implies that olivine was in a reaction relationship with an intermediate alkalic magma in both the intruded magmas at shallow depth and in the magma chamber at great depth. This is the cause of the olivine compositional gap in the high-K volcanic suite. Titanbiotite is a major reaction product.ZusammenfassungHaupt- und Spurenelementdaten von vier alkalischen gabbroiden, zwei monzonitische Haupt- und Spurenelementdaten von vier alkalischen gabbroiden, zwei monzonitische und neun syenitischen Einschlüssen von Ulreung Island, Korea, sowie analytische Daten der Mineralkomponenten werden vorgelegt. Obwohl der Hauptelementchemismus andeutet, daß die plutonischen Intrusionen und die vergesellschafteten vulkanischen Gesteine comagmatisch sind, zeigen die Spurenelementdaten, daß diese nicht eine einfache Magmenlinie darstellen. Außerdem zeigen die mineralogischen Daten an, daß die Gesteine wahrscheinlich keine Kumulate vom Boden der Magmenkammer sind, von welcher die beobachteten vulkanischen Gesteine herstammen. In den plutonischen Gesteinen kristallisierte Titan-Biotit früher als der Kaersutit. In den vulkanischen Gesteinen ist diese Reihenfolge jedoch umgekehrt. Die trachitischen/phonolitischen Gesteine enthalten im Gegensatz zu den plutonischen Einschlüssen Fe-reiche Olivin-Phenokrysten. Diese Unterschiede können durch die Annahme erklärt werden, daß die untersuchten plutonischen Gesteine bestimmte Kumulate eines intrusiven Körpers sind, der in geringerer Tiefe als das Magmenreservoir unterhalb der Inseln erstarrte. Petrographische Kennzeichen von gabbroischen Einschlüssen deuten darauf hin, daß der Olivin wahrscheinlich mit der Schmelze reagiert hat und Titan-Biotit bildete. Ein Vergleich der petrographischen Daten der vulkanischen Gesteine Vergleich der petrographischen Daten der vulkanischen Gesteine läßt ebenfalls den Schluß zu, daß Olivin mit einem intermediären alkalischen Magma in beiden, dem intrudierten Magma in geringer Tiefe und der Magmakammer in großer Tiefe, reagierte. Dies ist der Grund für die Lücke in der Olivinzusammensetzung in der Kalium-reichen vulkanischen Suite. Titan-Biotit ist ein Hauptreaktionsprodukt.