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Geochemistry and petrology of black opal in the pegmatites from Volyn (Ukraine)

Black opal is a rare variety of opal-CT, which is pigmented by organic matter (OM) and can therefore be considered as an example of geo-bio interaction (Gouzy et al., 2025). The locality of Volyn, Ukraine with its famous chamber pegmatites is well-known for interaction between OM and igneous rocks (Franz et al., 2017). The locality was recently renamed Khoroshiv, but because in the geological-mineralogical literature the name Volyn was introduced, we use this name here. The intrusion of the pegmatites is closely connected to the intrusion of the host rocks, granites of the southwestern part of the Korosten Pluton, and the intrusion age was determined as 1.76 Ga (Shumlyanskyy et al., 2021). OM was identified as kerite (fossilized remains of organisms; Franz et al., 2023, and references therein), and in fluid inclusions in beryl and topaz (Vozniak et al., 2012; Vozniak and Pavlyshin, 2008). Furthermore, formation of NH4-bearing feldspar (buddingtonite) and muscovite (tobelite) in breccia (identified together with the pegmatites) point to the interaction between decayed OM and the igneous minerals (Franz et al., 2017). The timing of the interaction between OM and igneous (and other) fluids is an important question (Franz et al., 2024), and therefore we also give age constraints on the formation of the black opal, which from textural arguments seems to be one of the latest mineral formations. We give detailed information about the sample sites, the macroscopic features of the samples of different types of opal, and the analytical procedures. The description of the black opal samples is presented in images from secondary electron microscopy (SEM), back-scattered electron images (BSE) obtained with by electron microprobe (EMPA), element distribution maps obtained by µXRF (X-ray fluorescence), Fourier-transformed infrared spectroscopy (IR), and X-ray powder (XRD) characterization. Chemical analyses were obtained by wave-length dispersive (WDS) analyses with the EMPA as well as by energy-dispersive (EDX) analyses with both the SEM and the EMPA instruments, to identify and characterize inclusions in the black opal. Trioctahedral Li-mica (polylithionite) is included by opal in one sample, and because this type of mica has not been described in detail from the Volyn peg-matites, we present the EMPA analytical data here in detail. The presence of OM, which is known to absorb U in sufficient amounts, allows dating by the U-Pb decay system. The results of the isotopic dating with the laser-ablation sector-field inductively-coupled mass spectroscopy system (LA-SF-ICP-MS) is presented for the selected individual do-mains in three samples. The operating conditions are summarized in a separated pdf document.

Laser ablation inductively coupled mass spectrometry trace elements analyses of Li-rich micas of Pan-African pegmatites in Mozambique

This data report presents the in-situ LA-ICP-MS trace element geochemistry of the micas of the Pan-African rare-element pegmatites of the Alto Ligonha Pegmatite District in northern Mozambique. The pegmatites contain Li-rich micas and primary Li aluminosilicates, such as spodumene. Five Alto Ligonha pegmatites, Naípa, Muiâne, Napepesso West, Nanro, and Natxepo, were investigated to better understand the fractionation of pegmatite melts leading to Li enrichment, utilizing e.g. the trace element chemistry of mica from different parts of these pegmatites. Micas collected from the wall zone, intermediate zone and core zone of the studied pegmatites show high but also highly variable concentrations of the incompatible elements like Li, Rb, Cs, Be, and Ta. Very strong pegmatite-internal fractionation is recorded by the mica chemistry of the Naípa, Muiâne and Nanro pegmatites. In these pegmatites, Li2O in white micas measured with LA-ICP-MS increases from 0.1-1.4 wt.% in the wall zone, to 0.3-1.7 wt.% in the intermediate zone, 1.5-3.8 wt.% in the core zone and up to 5.4 wt.% in the pockets. The data record extreme Li enrichment during the final crystallization stage.

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