The Cycladic blueschist belt, Greece, is mostly submerged below sea level and regional correlations are difficult to establish. Marbles are widespread within the belt and locally used as marker horizons to subdivide monotonous schist sequences. However, owing to the lack of distinctive petrographic characteristics, the marbles have not been used for island-to-island correlations. This study aims to investigate the potential of Sr-, C- and O-isotope compositions of marbles as a tool for unravelling the litho- and/or tectonostratigraphic relationships across the Cycladic islands, and as a proxy for the time of sediment formation. For this purpose, we have studied metamorphic carbonate rocks from the islands of Tinos, Andros, Syros, Sifnos and Naxos. Identical 87Sr/86Sr values for certain marble horizons occurring on Tinos, Andros and Sifnos are interpreted to document coeval regional carbonate precipitation. The 87Sr/86Sr values of the apparently least altered samples intersect the seawater curve multiple times within the most likely time interval of original carbonate precipitation (< 240 Ma; as indicated by previously published ion probe U–Pb zircon data) and thus an unequivocal age assignment is not possible. Very broad temporal correlations are possible, but more subtle distinctions are not feasible. On Andros, the overlapping Sr-isotope values of marbles representing the lowest and highest parts of the metamorphic succession are in accordance with a model suggesting isoclinal folding or thrusting of a single horizon, or very fast sedimentation. In contrast, distinct 87Sr/86Sr values for samples from Tinos, representing different levels of the metamorphic succession, suggest that these rocks represent a temporal succession and not the tectonic repetition of a single horizon. Based on Sr-, O- and C-isotope characteristics alone the time equivalence of marbles occurring on different islands could not be documented unambiguously. However, by using various combinations of these parameters, some occurrences can be discriminated from the overall sample population. The new data further accentuate the general potential of coupled Sr-, C- and O-isotope characteristics for identification of archaeological provenance and complement existing datasets for Aegean marbles.

Determining the timing or frequency of movement of fish and the relative importance of different habitats is difficult. Advances in otolith chemical techniques and interpretations (including elemental ratios and stable isotopes) suggest that this is a powerful method for determining movement of fish. To date, the majority of applications have involved marine fish, however, otolith chemistry has the potential to determine movements of diadromous and freshwater fish; I therefore review freshwater applications of otolith chemistry in this paper. Despite some limitations regarding strontium:calcium (Sr:Ca) ratios (e.g. Sr concentration of the water is not always measured, Sr:Ca ratios in freshwater can exceed marine waters, and mixed results for the relationship between otolith Sr and salinity), they have been widely used for a variety of applications involving diadromous species and more recently freshwater fish. In addition, barium:calcium (Ba:Ca) ratios have recently been used to determine movements of diadromous and estuarine species, as ambient ratios are possibly linked to environmental flows. Several studies have also investigated the use of multielemental otolith composition to discriminate between groups of fish collected from different lake or river systems, but a wider range of applications are possible. Several applications of Sr isotopes have also been investigated, most of which is focused on salmonids (e.g. distinguishing fish from different river systems, determining movement history of individual fish). Relatively few studies have investigated the use of other isotopes (e.g. oxygen, sulphur) for determining movements. Otolith elemental ratios and stable isotopes have great potential to determine movements of freshwater species, with possible applications likely to increase as analytical technology improves.

The prominent felsic granulites in the southern part of the Bohemian Massif (Gföhl Unit, Moldanubian Zone), with the Variscan (∼340 Ma) high-pressure and high-temperature assemblage garnet+quartz+hypersolvus feldspar ± kyanite, correspond geochemically to slightly peraluminous, fractionated granitic rocks. Compared to the average upper crust and most granites, the U, Th and Cs concentrations are strongly depleted, probably because of the fluid and/or slight melt loss during the high-grade metamorphism (900–1050°C, 1·5–2·0 GPa). However, the rest of the trace-element contents and variation trends, such as decreasing Sr, Ba, Eu, LREE and Zr with increasing SiO2 and Rb, can be explained by fractional crystallisation of a granitic magma. Low Zr and LREE contents yield ∼750°C zircon and monazite saturation temperatures and suggest relatively low-temperature crystallisation. The granulites contain radiogenic Sr (87Sr/86Sr340 = 0·7106–0·7706) and unradiogenic Nd ( = − 4·2 to − 7·5), indicating derivation from an old crustal source. The whole-rock Rb–Sr isotopic system preserves the memory of an earlier, probably Ordovician, isotopic equilibrium.

Contrary to previous studies, the bulk of felsic Moldanubian granulites do not appear to represent separated, syn-metamorphic Variscan HP–HT melts. Instead, they are interpreted as metamorphosed (partly anatectic) equivalents of older, probably high-level granites subducted to continental roots during the Variscan collision. Protolith formation may have occurred within an Early Palaeozoic rift setting, which is documented throughout the Variscan Zone in Europe.

The current underlying assumption in most geochemical studies of granitic rocks is that granitic magmas reflect their source regions. However, the mechanisms by which source rocks control the intensive and compositional parameters of the magmas remain poorly known. Recent experimental data are used to evaluate the ‘source rock model’ and to discuss controls of (1) redox states and (2) the Sr isotopic compositions of granitic magmas.

Experimental studies have been performed in parallel on biotite-muscovite and tourmaline-muscovite leucogranites from the High Himalayas. Results under reducing conditions ( = FMQ – 0·5) at 4 kbar and variable suggest that the tourmaline-muscovite granite evolved under progressively more oxidising conditions during crystallisation, up to values more than four log units above the FMQ buffer. Leucogranite magmas thus provide an example of the control of redox conditions by post-segregation rather than by partial melting processes.

Other experiments designed to test the mechanisms of isotopic equilibration of Sr during partial melting of a model crustal assemblage show that kinetic factors can dominate the isotopic signature in the case of source rocks not previously homogenised during an earlier metamorphic event. The possibility is therefore raised that partial melts may not necessarily reflect the Sr isotopic composition of their sources, weakening in a fundamental way the source rock model.