Geochemical characteristics of Yamadağı volcanics in central east Anatolia: an example from collision-zone volcanism

Neogene Yamadağı volcanic rocks consist of basaltic trachyandesite, trachyandesite, andesite, and dacite. The major- and trace-element chemistry indicates that the lavas are dominantly calc-alkaline and mildly alkaline in character, sodic in nature, and intermediate to acidic in composition. REE and trace-element patterns of volcanic rocks are similar to those typical of within plate magmatics. Volcanic rocks have low ⁸⁷Sr/⁸⁶Sr (0.70389–0.70633) and high ¹⁴³Nd/¹⁴⁴Nd ratios (0.51267–0.51276) and mostly plot within the mantle array of the isotope ratio diagram. The linear correlations among ⁸⁷Sr/⁸⁶Sr−¹⁴³Nd/¹⁴⁴Nd, SiO₂−⁸⁷Sr/⁸⁶Sr and SiO₂−¹⁴³Nd/¹⁴⁴Nd isotope ratios in the volcanics suggest that fractional crystallization combined with minor assimilation was an important process within the collision zone.     

Cookeite LiAl4(Si3Al)O10(OH)8: Experimental study and thermodynamical analysis of its compatibility relations in the Li2O−Al2O3−SiO2−H2O system

Three reactions limiting the stability field of the di-trioctahedral chlorite cookeite in the presence of quartz, in the system Li₂O−Al₂O₃−SiO₂−H₂O (LASH) have been reversed in the range 290–480°C, 0.8–14 kbar, using natural material close to the end member composition. Combining our results with known and estimated thermodynamic properties of the other minerals belonging to the LASH system, the enthalpy (-8512200 J/mol) and the entropy (504.8 J/mol^*K) of cookeite are calculated by a feasible solution space approach. The knowledge of these values allowed us to draw the first P−T phase diagram involving both the hydrated Li-aluminosilicates cookeite and bikitaite, which is applicable to a large variety of natural rock systems. The low thermal extent of the stability field of cookeite+quartz (260–480°C) makes cookeite a valuable indicator of low temperature conditions within a wide range of pressure (1–14 kbar).     

Étude expérimentale des transformations de phase dans un gradient thermique : application au granite de Soultz-sous-Forêts,France

The circulation of an injected fluid in the deep granite of the Soultz-sous-Forêts HDR (‘Hot Dry Rock’) site causes important textural and mineralogical modifications. In order to determine the potential crystallization sequences along the fluid pathway, several experiments under thermal gradient were conducted at 600 bar (between 300 and 200 °C). After 40 days, the observed sequences of the newly formed products along the thermal gradient are always as follows, from high to low temperatures: quartz, feldspars, and finally interstratified clays, this implying a significant mobility of aluminium in the solution. To cite this article: A. Baldeyrou et al., C. R. Geoscience 335 (2003).     

Multistage growth of Fe–Mg–carpholite and Fe–Mg–chloritoid,from field evidence to thermodynamic modelling

We provide new insights into the prograde evolution of HP/LT metasedimentary rocks on the basis of detailed petrologic examination, element-partitioning analysis, and thermodynamic modelling of well-preserved Fe–Mg–carpholite- and Fe–Mg–chloritoid-bearing rocks from the Afyon Zone (Anatolia). We document continuous and discontinuous compositional (ferromagnesian substitution) zoning of carpholite (overall X _Mg = 0.27–0.73) and chloritoid (overall X _Mg = 0.07–0.30), as well as clear equilibrium and disequilibrium (i.e., reaction-related) textures involving carpholite and chloritoid, which consistently account for the consistent enrichment in Mg of both minerals through time, and the progressive replacement of carpholite by chloritoid. Mg/Fe distribution coefficients calculated between carpholite and chloritoid vary widely within samples (2.2–20.0). Among this range, only values of 7–11 correlate with equilibrium textures, in agreement with data from the literature. Equilibrium phase diagrams for metapelitic compositions are calculated using a newly modified thermodynamic dataset, including most recent data for carpholite, chloritoid, chlorite, and white mica, as well as further refinements for Fe–carpholite, and both chloritoid end-members, as required to reproduce accurately petrologic observations (phase relations, experimental constraints, Mg/Fe partitioning). Modelling reveals that Mg/Fe partitioning between carpholite and chloritoid is greatly sensitive to temperature and calls for a future evaluation of possible use as a thermometer. In addition, calculations show significant effective bulk composition changes during prograde metamorphism due to the fractionation of chloritoid formed at the expense of carpholite. We retrieve P–T conditions for several carpholite and chloritoid growth stages (1) during prograde stages using unfractionated, bulk-rock XRF analyses, and (2) at peak conditions using compositions fractionated for chloritoid. The P–T paths reconstructed for the Kütahya and Afyon areas shed light on contrasting temperature conditions for these areas during prograde and peak stages.     

Temporal evolution of weathered cataclastic material in gravitational faults of the La Clapiere deep-seated landslide by mechanical approach

After a few years of research, the observation and the analysis of the deep-seated landslides suggest that these are mainly controlled by tectonic structures, which play a dominant role in the deformation of massif slopes. The La Clapière deep-seated landslide (Argentera Mercantour massif) is embedded in a deep-seated gravitational slope deformation affecting the entire slope, and characterized by specific landforms (trenches, scarps??). Onsite, the tangential displacement direction of the trenches and the scarps are controlled by the tectonic structures. The reactivation of the inherited fault in gravitational faults create a gouge material exposed to an additional mechanical and chemical weathering as well as an increased of leaching. The displacement of these reactivated faults gets increasingly important around the area of the La Clapière landslide and this since 3.6?ka BP. In this study, mechanical analysis and grain size distributions were performed and these data were analysed according to their proximity the La Clapiere landslide and times of initiation of the landslide by ¹⁰Be dating. Triaxial test results show that the effective cohesion decreases and the effective angle of internal friction increases from the unweathered area to the weathered area. The whole distribution of the grain size indicates that the further the shear zone is open or developed, the further the residual material loses its finest particles. This paper suggests that the mechanical evolution along the reactivated fault is influenced by the leaching processes. For the first time, we can extract from these data temporal behaviour of the two main mechanical parameters (cohesion and angle of internal friction) from the beginning of the La Clapiere landslide initiation (3.6 ka BP) to now.     

Along-strike variations of P–T conditions in accretionary wedges and syn-orogenic extension,the HP–LT Phyllite–Quartzite Nappe in Crete and the Peloponnese

Syn-orogenic detachments in accretionary wedges make the exhumation of high-pressure and low-temperature metamorphic rocks possible with little erosion. The velocity of exhumation within the subduction channel or the accretionary complex, and thus the shape of P–T paths, depend upon the kinematic boundary conditions. A component of slab retreat tends to open the channel and facilitates the exhumation. We document the effect of slab retreat on the shape of P–T paths using the example of the Phyllite–Quartzite Nappe that has been exhumed below the Cretan syn-orogenic detachment during the Miocene in Crete and the Peloponnese. Data show a clear tendency toward colder conditions at peak pressure and during exhumation where the intensity of slab retreat is larger. This spatial evolution of P–T gradient is accompanied with an evolution from a partly coaxial regime below the Peloponnese section of the detachment toward a clearly non-coaxial regime in Crete.     

Long-term fluid circulation in extensional faults in the central Catalan Coastal Ranges: P–T constraints from neoformed chlorite and K-white mica

The neoformation of chlorite and K-white mica in fault rocks from two main faults of the central Catalan Coastal Ranges, the Vallès and the Hospital faults, has allowed us to constrain the P–T conditions during fault evolution using thermodynamic modeling. Crystallization of M1 and M2 muscovite and microcline occured as result of deuteric alteration during the exhumation of the pluton (290 °C > T > 370 °C) in the Permian. After that, three tectonic events have been distinguished. The first tectonic event, attributed to the Mesozoic rifting, is characterized by precipitation of M3 and M4 phengite together with chlorite and calcite C1 at temperatures between 190 and 310 °C. The second tectonic event attributed to the Paleogene compression has only been identified in the Hospital fault with precipitation of low-temperature calcite C2. The shortcut produced during inversion of the Vallès fault was probably the responsible for the lack of neoformed minerals within this fault. Finally, the third tectonic event, which is related to the Neogene extension, is characterized in the Vallès fault by a new generation of chlorite, associated with calcite C4 and laumontite, formed at temperatures between 125 and 190 °C in the absence of K-white mica. Differently, the Hospital fault is characterized by the precipitation of calcite C3 during the syn-rift stage at temperatures around 150 °C and by low-temperature fluids precipitating calcites C5, C6 and PC1 during the post-rift stage. During the two extensional events (Mesozoic and Neogene), faults acted as conduits for hot fluids producing anomalous high geothermal gradients (50 °C/km minimum).     

Experimental study of chloritoid stability at high pressure and various fO2 conditions

The reaction chloritoid (ctd)=almandine (alm)+diaspore+H₂O (CAD) has been reversed using Fe³⁺-free synthetic chloritoid and almandine, under fO₂ conditions of the solid oxygen buffer Fe/FeO (CADWI), and using partially oxidized synthetic minerals under fO₂ conditions of the solid oxygen buffer Ni/NiO (CADNNO). Experiments have been conducted between 550 and 700°C, 25 and 45 kbar. The equilibrium pressure and temperature conditions are strongly dependent on the fO₂ conditions (CADNNO lies some-what 50°C higher than CADWI). This can be explained by a decrease in aH₂O for experiments conducted on the Fe/FeO buffer, and a decrease in actd and aalm (through incorporation of ferric iron preferentially in chloritoid) for experiments conducted on the Ni/NiO buffer. The H₂O activity has been calculated using the MRK equation of state, and the values obtained checked against the shift of the equilibrium diaspore=corundum+H₂O bracketed on the Fe/FeO buffer and under unbuffered fO₂ conditions. For fO₂ buffered by the assemblage Fe/FeO, aH₂O increases with pressure from about 0.85 at 600°C, 12 kbar to about 0.9 at 605°C, 25 kbar and 1 above 28 kbar. For fO₂ buffered by the assemblage Ni/NiO, aH₂O=1. The aH₂O decrease from Ni/NiO to Fe/FeO is, however, too small to be entirely responsible for the temperature shift between CADNNO and CADWI. In consequence, the amount of ferric iron in almandine and chloritoid growing in the CADNNO experiments must be significant and change along the CADNNO, precluding calculation of the thermodynamic properties of chloritoid from this reaction. Our experimental data obtained on the Fe/FeO buffer are combined, using a thermodynamic analysis, with Ganguly's (1969) reversal of the reaction chloritoid=almandine+corundum +H₂O (CAC) on the same oxygen buffer. Experimental brackets are mutually consistent and allow extraction of the thermodynamic parameters H ^o f,ctd and S ^octd. Our thermodynamic data are compared with others, generally calculated using Ganguly's bracketing of CACNNO. The agreement between the different data sets is relatively good at low pressure, but becomes rapidly very poor toward high pressure conditions. Using our thermodynamic data for chloritoid and K_D=(Fe³⁺/Al)ctd/(Fe³⁺/Al)alm estimated from natural assemblages, we have calculated the composition of chloritoid and almandine growing from CADNNO and CACNNO. The Fe³⁺ content in chloritoid and almandine increases with pressure, from less than 0.038 per FeAl₂SiO₅(OH)₂ formula unit at 10 kbar to at least 0.2 per formula unit above 30 kbar. This implies that chloritoid and almandine do contain Fe³⁺ in most natural assemblages. The reliability of our results compared to natural systems and thermodynamic data for Mg-chloritoid is tested by comparing the equilibrium conditions for the reaction chloritoid+quartz=garnet (gt)+kyanite+H₂O (CQGK), calculated for intermediate Fe–Mg chloritoid and garnet compositions, from the system FASH and from the system MASH. For 0.65<(XFe)gt<0.8, CQKG calculated from FASH and MASH overlap for K_D=(Mg/Fe)ctd/(Mg/Fe)gt=2. This is in good agreement with the K_D values reported from chloritoid+garnet+quartz+kyanite natural assemblages.