A Laser Raman microspectrometry method was applied to metamorphic quartz in quartz-eclogite-, epidote-amphibolite-, and amphibolite-facies rocks to assess the quantitative correlation between the Raman frequency shift and metamorphic pressure. Quartz crystals sealed in garnet and other phases have a higher frequency shift than those in the matrix. Furthermore, the quartz inclusions show a frequency shift specifi c to the individual host crystals in eclogites (garnet ≈ kyanite > omphacite ≈ epidote). These observations imply that the residual pressures retained by quartz inclusions depend on elastic parameters of the host crystals, as discussed by previous researchers. The Raman frequency shift of quartz inclusions in garnet systematically increases with increasing peak metamorphic pressures from the amphibolite facies (0.30-0.55 GPa/470-570 °C), through the epidote-amphibolite facies (0.8-1.1 GPa/470-635 °C) to the quartz-eclogite facies (2.1-2.5 GPa/660-710 °C). Calibrations based on experimental work suggest that the measured Raman frequency shifts signify residual pressures of 0.1-0.2, 0.4-0.6, and 0.8-1.0 GPa for these three groups of metamorphic rocks, respectively. Normal stresses (internal pressures) of quartz inclusions in garnet, numerically simulated with an elastic model, and inferred pressure-temperature conditions at peak metamorphic stage are compatible with the residual pressures estimated from the frequency shifts. Laser Raman microspectroscopic analysis of quartz is a simple and effective method for (1) comparison of pressure conditions in metamorphic rocks formed under various pressure-temperature conditions, and (2) detection of a higher-pressure signature in metamorphic rocks extensively recrystallized during the subsequent exhumation and hydration stage.

No abstract

No abstract

No abstract

Zircon separates from one jadeitite sample (JJ) from Tone, Japan and one from Guatemala (GJ) were studied for mineral inclusions, age dating, trace-element determination and Hf isotope analysis. These zircons can be categorized into two types. Type I (igneous) zircons are characterized by the presence of mineral inclusions, among others K-feldspar, which is not present in jadeitite matrix. They also show higher Th/U ratios, larger Ce anomalies and higher 176 Lu/ 177 Hf ratios. Type II (metasomatic/solutionprecipitate) zircons contain omphacite/jadeite inclusions and exhibit lower Th/U ratios, smaller Ce anomalies and lower 176 Lu/ 177 Hf ratios. Both types of zircons display high eHf(t) values, slightly lower than the depleted mantle evolution line. The JJ sample contains both type I and II zircons. SHRIMP and geochemical data indicate that this jadeitite sample was formed through the mechanism of wholesale metasomatic replacement at $80 Ma from an igneous protolith of juvenile origin with an age of 136 AE 2 Ma. The GJ sample contains only type II zircons and may have formed through a mechanism of, or close to, vein precipitation at 98 AE 2 Ma. The two samples therefore testify that both mechanisms may have been in operation during jadeitite formation. Based on Hf isotope composition of type I zircons and the back-calculated REE pattern of the presumed protolith, the geochemical characteristics of the protolith of the Tone jadeitite were shown to be similar to those of oceanic plagiogranites derived from partial melting of cumulate gabbros or subduction-zone adakitic granites originated from partial melting of subducted oceanic crust. The latter, however, is a more probable candidate because the former is known to be poor in K 2 O, which, in contrast, is a notable chemical component in Tone jadeitite. On the basis of the available data, it is also suggested that the protolith, the physicochemical conditions and the extent of jadeitization may all play a role in dictating the chemical variations of jadeitites.