Metasedimentary rocks generally contain carbonaceous material (CM) deriving from the evolution of organic matter originally present in the host sedimentary rock. During metamorphic processes, this organic matter is progressively transformed into graphite s.s. and the degree of organisation of CM is known as a reliable indicator of metamorphic grade. In this study, the degree of organisation of CM was systematically characterised by Raman microspectroscopy across several Mesozoic and Cenozoic reference metamorphic belts. This degree of organisation, including within‐sample heterogeneity, was quantified by the relative area of the defect band (R2 ratio). The results from the Schistes Lustrés (Western Alps) and Sanbagawa (Japan) cross‐sections show that (1) even through simple visual inspection, changes in the CM Raman spectrum appear sensitive to variations of metamorphic grade, (2) there is an excellent agreement between the R2 values calculated for the two sections when considering samples with an equivalent metamorphic grade, and (3) the evolution of the R2 ratio with metamorphic grade is controlled by temperature (T). Along the Tinos cross‐section (Greece), which is characterised by a strong gradient of greenschist facies overprint on eclogite facies rocks, the R2 ratio is nearly constant. Consequently, the degree of organisation of CM is not affected by the retrogression and records peak metamorphic conditions. More generally, analysis of 54 samples representative of high‐temperature, low‐pressure to high‐pressure, low‐temperature metamorphic gradients shows that there is a linear correlation between the R2 ratio and the peak temperature [T(°C) = −445 R2 + 641], whatever the metamorphic gradient and, probably, the organic precursor. The Raman spectrum of CM can therefore be used as a geothermometer of the maximum temperature conditions reached during regional metamorphism. Temperature can be estimated to ± 50 °C in the range 330–650 °C. A few technical indications are given for optimal application.

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Terra Nova, 22, 354–360, 2010 Abstract The Raman spectrum of carbonaceous material (CM) from advanced diagenesis (∼200 °C) to low‐grade metamorphism (∼320 °C) is documented in the Helvetic flysch of the Glarus Alps (Switzerland). The spectrum is complex, with several defect bands at ∼1200 (D4), ∼1350 (D1), ∼1500 (D3) and ∼1620 (D2) cm−1. We document the evolution of these bands relative to the ‘graphite’ G band with increasing metamorphic grade, and we show that this qualitative evolution may be used as a proxy for temperature in the Glarus Alps. We develop a robust peak‐fitting method and propose quantitative parameters that may be used as proxies for thermal metamorphism in this region. Further work in other geological contexts is needed to assess whether the spectral evolution observed in the Glarus Alps may be generalized and to critically assess the potential for calibrating a general, empirical and quantitative thermometer based on the Raman spectrum of CM in low‐grade rocks.

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Abstract. An increasing number of field examples in mountain belts show that the formation of passive margins during extreme continent thinning may occur under conditions of high to very high thermal gradient beneath a thin cover of syn-rift sediments. Orogenic belts resulting from the tectonic inversion of distal margins and regions of exhumed continental mantle may exhibit high-temperature, low-pressure (HT-LP) metamorphism and coeval syn-extensional, ductile deformation. Recent studies have shown that the northern flank of the Pyrenean belt, especially the North Pyrenean Zone, is one of the best examples of such inverted hot, passive margin. In this study, we provide a map of HT-LP metamorphism based on a data set of more than 100 peak-temperature estimates obtained using Raman spectroscopy of the carbonaceous material (RSCM). This data set is completed by previous PT (pressure and temperature) estimates based on mineral assemblages, and new 40 Ar-39 Ar (amphibole, micas) and U-Pb (titanite) ages from metamorphic and magmatic rocks of the North Pyrenean Zone. The implications on the geological evolution of the Cretaceous Pyrenean paleomargins are discussed. Ages range mainly from 110 to 90 Ma, and no westward or eastward propagation of the metamorphism and magmatism can be clearly identified. In contrast, the new data reveal a progressive propagation of the thermal anomaly from the base to the surface of the continental crust. Focusing on the key localities of the Mauléon basin, Arguenos-Moncaup, Lherz, Boucheville and the Bas-Agly, we analyze the thermal conditions prevailing during the Cretaceous crustal thinning. The results are synthetized into a series of three regional thematic maps and into two detailed maps of the Arguenos-Moncaup and Lherz areas. The results indicate a first-order control of the thermal gradient by the intensity of crustal thinning. The highest grades of metamorphism are intimately associated with the areas where subcontinental mantle rocks have been unroofed or exhumed.

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The key cation-sites M3 and A1 (and, in principle, M2) determine the root name. In both clinozoisite and allanite subgroups no prefix is added to the root name if M1 = Al. The prefixes ferri, mangani, chromo, and vanado indicate dominant Fe 3+ , Mn 3+ , Cr 3+ , and V 3+ on M1, respectively. In the dollaseite subgroup no prefix is added to the root name if M1 = Mg. Otherwise a proper prefix must be attached; the prefixes ferro and mangano indicate dominant Fe 2+ and Mn 2+ at M1, respectively. The dominant cation on A2 (other than Ca) is treated according to the Extended Levinson suffix designation. This simple nomenclature requires renaming of the following approved species: Niigataite (old) = clinozoisite-(Sr) (new), hancockite (old) = epidote-(Pb) (new), tweddillite (old) = manganipiemontite-(Sr) (new). Minor modifications are necessary for the following species: Strontiopiemontite (old) = piemontite-(Sr) (new), androsite-(La) (old) = manganiandrosite-(La) (new). Before a mineral name can be assigned, the proper subgroup has to be determined. The determination of a proper subgroup is made by the dominating valence at M3, M1, and A2 expressed as M 2+ and or M 3+ , not by a single, dominant ion (i.e., Fe 2+ , or Mg, or Al). In addition, the dominant valence on O4: X -or X 2-must be ascertained. The dominant trivalent cation on M3 determines the name, whereas the A2 cation appearing in the suffix has to be selected from among the divalent cations. (2) Allanite and dollaseite subgroups: For the sites involved in the charge compensation of a heterovalent substitution in A2 and O4 (i.e. M3 in the allanite subgroup; M3 and M1 in the dollaseite subgroup), identification of the relevant end-member formula must take into account the dominant divalent charge-compensating octahedral cation (M 2+ ) and not the dominant cation in these sites.Formal guidelines and examples are provided in order to determine a mineral "working name" from electron-microprobe analytical data.