Temperature-resolved analyses of volatiles from Mid-Ocean-Ridge-Basalt (MORB) and vitreous basaltic rims were carried out to investigate the total volatile contents of basaltic melts and the influence of magma contamination on the degassing behaviour of volcanic rocks. With respect to the sources of methane evolution from the MORB the investigations are taken into consideration, the hydrocarbon (HC) release especially from the melt. The current paper presents data for H 2O, CO 2, SO 2, He, H 2, HF, HCl, CO, N 2, O 2, and HC degassing profiles of samples from the MORB sampling cruise 02.10.1983–11.11.1983 with FS Sonne 28 during the GEMINO-1 project near the Carlsberg Ridge (CR) and the Mid-Indian-Ocean-Ridge (MIOR). It aims to estimate the magnitude and nature of source magma volatiles and contamination (crustal material, seawater, atmospheric gases). The degassing of H 2O, CO 2, HCs as well as sulphur and chlorine species, or O 2 from vitreous specimens shows characteristic differences associated with sample position with respect to the lava surface. From the water release by bubbling and diffusion above 700 °C it must be concluded that any assimilation of sea water in vitreous rim is very low. The water content in the vitreous rim is about 0.1–0.2 wt%. The low interaction of melt with sea water is supported by the missing of a significant release of chlorine species during the heat treatment of the sample up to 1450 °C. Mixed H 2O/CO 2 bubbles escape between 700 and 800 °C from the vitreous rim. The CO 2 release in the temperature range of 1060–1170 °C from the basalt and the vitreous rim is interpreted as an indication for the primary carbon-dioxide content in the melt. Above 1100 °C CO 2 and SO 2 are evolved by both diffusion and small bubbles. The quantities of CO 2 in the vitreous rim and the basalt are similar (between 0.05 and 0.15 wt%), whereas the quantities of SO 2 escaping both from the vitreous rim and the crystalline basalt are between 0.013 and 0.024 wt%. Simultaneous with the CO 2 release by bubbling, HC species, especially CH fragments, were observed. The fact that the temperature of release maxima are above 1050 °C in both the vitreous rim and in the basalt is an indication for a geogenetic origin of HCs, e.g. methane. A low temperature of release for methane, which is consistent with biogenetic HC, was observed from the gas-release profiles of the basalts only. The maxima of the low-temperature gas releases are between 80 and 200 °C with a high correlation between the fragments m/ z 13 and m/ z 15. This correlation is a significant indication for a methane release. The oxygen release profiles of vitreous and crystalline basalts give significant indications for oxygen fugacity below the (QMF) of basaltic magma. Secondary minerals, generated by alteration of basaltic rocks, can be characterized by gas release profiles (GRPs) due to their decomposition in the temperature range below 800 °C. Only in the basalt were there observed indications of alteration processes. Small traces of carbonates (<0.0001 wt%) were detected by the gas release during the decomposition. Processes of degassing at temperatures higher than 800 °C are correlated to volatiles in the melt and to fluid inclusions of the minerals. There are no obvious correlations in the degassing characteristics between H 2O, CO 2 and SO 2. The different maxima of the degassing velocity, especially of CO 2, and SO 2, are indications of the different bonding forces of the site occupancy of the volatiles in the melt and in the glass. A micelle model for bonding sites in the basaltic glass for dissolved volatiles is discussed.
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