ALBERT

Description: We determined the bromine isotope compositions of magmatic and hydrothermal sodalite (Na8Al6Si6O24Cl2) and tugtupite (Na8Al2Be2Si8O24Cl2) from the Ilímaussaq intrusion in South Greenland, in order to constrain the Br isotope composition of the melt and hydrothermal fluids from which these minerals were formed. Early formed magmatic sodalite has high Br contents (138 ± 10 µg/g, n = 5) and low δ81Br values (+0.23 ± 0.07‰). Late stage hydrothermal sodalite has lower Br contents (53±10 µg/g, n = 5) and higher δ81Br values (+0.36 ± 0.08‰). Tugtupite that forms at even later stages shows the lowest Br contents (26 ± 2 µg/g, n = 2) and the highest δ81Br values (+0.71 ± 0.17‰). One hydrothermal sodalite has a Br concentration of 48 ± 9 µg/g and an exceptionally high δ81Br of 0.82 ± 0.12‰, very similar to the δ81Br of tugtupites. We suggest that this may be a very late stage sodalite that possibly formed under Be deficient conditions. The data set suggests that sodalite crystallises with a negative Br isotope fractionation factor, which means that the sodalite has a more negative δ81Br than the melt, of −0.3 to −0.4‰ from the melt. This leads to a value of +0.5 to +0.6‰ relative to SMOB for the melt from which sodalite crystallises. This value is similar to a recently published δ81Br value of +0.7‰ for very deep geothermal fluids with very high R/Ra He isotope ratios, presumably derived from the mantle. During crystallisation of later stage hydrothermal sodalite and the Be mineral tugtupite, δ81Br of the residual fluids (both melt and hydrothermal fluid) increases as light 79Br crystallises in the sodalite and tugtupite. This results in increasing δ81Br values of later stage minerals that crystallise with comparable fractionation factors from a fluid with increasingly higher δ81Br values.

Description: The southern part of the eastern branch of the East African Rift is characterized by extensive volcanic activity since the late Miocene. In the Crater Highlands, part of the North Tanzanian Divergence zone, effusive and pyroclastic rocks reflect nephelinitic and basaltic compositions that formed between 4·6 and 0·8 Ma. The former are best represented by the Sadiman volcano (4·6–4·0 Ma) and the latter occur in the giant Ngorongoro crater (2·3–2·0 Ma), the Lemagarut volcano (2·4–2·2 Ma) and as a small volcanic field in the Laetoli area (2·3 Ma), where basaltic rocks known as Ogol lavas were erupted through fissures and several cinder cones. Compositionally, they are alkaline basalts with 46·0–47·9 wt% SiO2, 3·0–4·3 wt% of Na2O + K2O, Mg# of 61 to 55, and high Cr and Ni content (450–975 and 165–222 ppm respectively). Detailed textural and compositional analysis of the major minerals (olivine, clinopyroxene, plagioclase and spinel-group minerals) reveals the heterogeneity of the rocks. The primary mineral assemblage that crystallized from the Ogol magmas comprises macro- and microcrysts of olivine (Fo89·5–84·2), Cr-bearing diopside to augite, magnesiochromite–chromitess, magnetite–ulvöspinelss, andesine–oligoclasess and fluorapatite, with glass of phonolitic composition in the groundmass. All samples contain appreciable proportions of xenocrystic minerals of macro- and microcryst size, with large variations in both concentration and mineral populations between samples. Xenocrysts include olivine with reverse zonation (Fo84·1–72·5), rounded and embayed clinopyroxene cores of variable composition, anhedral Cr-free magnetite–ulvöspinelss and embayed oligoclase. These xenocrysts as well as variations in major and trace element contents, 87Sr/86Sr(i) (0·70377–0·70470) and 143Nd/144Nd(i) (0·51246–0·51261) ratios provide evidence of multi-stage magma mixing and mingling between Ogol and adjacent Lemagarut volcano basaltic melts with only very minor contamination by Precambrian granite–gneisses. Elevated alkalinity of Ogol lavas, which positively correlates with isotope ratios, and the presence of xenocrystic green core clinopyroxene, perovskite, schorlomite and titanite indicate additional mixing and mingling with evolved nephelinitic magmas and/or assimilation of nephelinitic Laetolil tuffs or foidolitic rocks related to the Sadiman volcano. Owing to their heterogeneity, estimates on the crystallization conditions for the Ogol rocks are difficult. Nevertheless, clinopyroxene–liquid thermobarometry indicates crystallization temperatures of around 1150–1220 °C and records upper-crustal depths of 3–12 km (1–4 kbar). Despite the fact that Ogol basalts are hybrid rocks that formed under open-system conditions with well-documented mixing and mingling processes, they seem to be the best examples closest to primary basaltic melts within the Crater Highlands.

Description: The Annaberg-Buchholz district is a classic occurrence of hydrothermal five-element (U-Ag-Bi-Co-Ni-As) veins in the Erzgebirge (Germany) with an historic production of ~8,700 metric tons (t) Co ore, 496 t U ore, and 26.9 t Ag. Multiple mineralization stages are recognized in polyphase veins hosted by Proterozoic paragneiss. Fluorite-barite-Pb-Zn mineralization occurs across the entire vertical profile of the district, whereas U and five-element stages are restricted to the upper 400 m below surface, coinciding with a graphite-rich gneiss lithology. Here, we present field and petrographic observations, electron probe microanalysis and fluid inclusion data, as well as thermodynamic calculations to characterize five-element and fluorite-barite-Pb-Zn associations, and to constrain the origin of the vertical zoning in the Annaberg-Buchholz district. Microthermometric analyses of fluid inclusions related to the fluorite-barite-Pb-Zn stage yield homogenization temperatures between 78° and 140°C and salinities between 21.9 and 27.7 equiv wt % (NaCl-CaCl2). A correlation of fluid inclusion Na/ (Na + Ca) ratios with salinity suggests fluid mixing as a likely precipitation mechanism and relates ore formation tentatively to regional tectonics of the Mesozoic opening of the Atlantic. Thermodynamic calculations indicate that U is more sensitive to reduction than As, predicting that arsenide minerals are precipitated more distally relative to uraninite upon reduction along the fluid-flow path. This implies that the observed vertical zoning is not a primary feature but is the result of hydrothermal remobilization. The observations made in the Annaberg-Buchholz district have general importance to the understanding of U-rich five-element mineralization and may be relevant for exploration targeting in unconformity-related U deposits.