The ⁴⁰Ar/³⁹Ar method applied to K-feldspars and muscovite has been often used to construct continuous thermal history paths between ~150–600 °C, which are usually applied to structural and tectonic questions in many varied geological settings. However, other authors contest the use of ⁴⁰Ar/³⁹Ar thermochronology because they argue that the assumptions are rarely valid. Here we review and evaluate the key assumptions, which are that (i) ⁴⁰Ar is dominantly redistributed in K-feldspars and muscovite by thermally-driven volume diffusion, and (ii) laboratory experiments (high temperatures and short time scales) can accurately recover intrinsic diffusion parameters that apply to geological settings (lower temperatures over longer time scales). Studies do not entirely negate the application of diffusion theory to recover thermal histories, although they reveal the paramount importance of first accounting for fluid interaction and secondary reaction products via a detailed textural study of single crystals. Furthermore, an expanding database of experimental evidence shows that laboratory step-heating can induce structural and textural changes, and thus extreme caution must be made when extrapolating laboratory derived rate loss constants to the geological past. We conclude with a set of recommendations that include minimum sample characterisation prior to degassing, an assessment of mineralogical transformations during degassing and the use of in situ dating.

Late Quaternary volcanoes of Sredinny Range (Kamchatka) attract geoscientists’ attention by their unusual geochemical features and geodynamic setting. They produced volcanic rocks that are enriched...

Most recent studies consider the formation of individual pegmatite bodies to be a fast process with estimated crystal growth rates reaching a walloping 10 m/day. This opinion is presumably underpinned by the traditional way of thinking of them as the end products of magmatic fractionation. Indeed, modelling has shown that if a pegmatite-forming substance with a temperature near granitic solidus intrudes into a much colder host rock, as recorded in some outcrops, it must cool rapidly. From here, a conclusion is made that the crystallisation must likewise be rapid. However, this view is challenged by several studies that published isotopic dates supported by petrological characterisation of the analysed materials, which suggested or can be used to suggest that some minerals in pegmatites grew over millions of years. Surprisingly, such in-depth work on the geochronology of individual pegmatite bodies is relatively uncommon, so it is early to make generalisations. Here, I highlight some of the existing evidence with the aim to stimulate further research into the timescales of pegmatite crystallisation, including the use of petrologically constrained isotopic dating.

This study focuses on Jurassic shallow intrusions and subvolcanic bodies from around Trudolyubovka village in the southwestern Crimea. All the rocks are similar in mineral composition and have similar geochemical features and occur in close spatial and geological association. This allows us to assign the intrusions to a single magmatic series and interpret them as differentiation products of a single parental melt. The investigation of melt inclusions in olivine from the most magnesian sample showed that the composition of igneous melts ranged from basalt to basaltic andesite of a moderately potassic subalkaline affinity. Compared with N-MORB, they are enriched in LILE, but have similar HFSE and REE contents. The early magmatic melts crystallized at temperatures ranging from 1240 to 1125°C, pressures of 6–8 kbar, and an oxygen fugacity of ΔQFM = +0.6; and later melts crystallized at 1090–940°C, ~1.5 kbar, and oxygen fugacity increasing from ΔQFM + 0.9 to ΔQFM + 2.3. The minimum pressure of groundmass crystallization was estimated as 40–60 bar. The primitive melts were formed in a mature island arc or an active continental margin setting by ~13% melting of a DMM-like source. The melting occurred at spinel-facies depths under the influence of a slab-derived fluid at a temperature 25°C below the dry peridotite solidus.