Carbonatites in a subduction system: The Pleistocene alvikites from Mt. Vulture (southern Italy)

We report here, for the first time, on the new finding of extrusive calciocarbonatite (alvikite) rocks from the Pleistocene Mt. Vulture volcano (southern Italy). These volcanic rocks, which represent an outstanding occurrence in the wider scenario of the Italian potassic magmatism, form lavas, pyroclastic deposits, and feeder dikes exposed on the northern slope of the volcano. The petrography, mineralogy and whole-rock chemistry attest the genuine carbonatitic nature of these rocks, that are characterized by high to very high contents of Sr, Ba, U, LREE, Nb, P, F, Th, high Nb/Ta and LREE/HREE ratios, and low contents of Ti, Zr, K, Rb, Na and Cs. The O–C isotope compositions are close to the “primary igneous carbonatite” field and, thus, are compatible with an ultimate mantle origin for these rocks. The Sr–Nd–Pb–B isotope compositions, measured both in the alvikites and in the silicate volcanic rocks, indicate a close genetic relationship between the alvikites and the associated melilitite/nephelinite rocks. Furthermore, these latter products are geochemically distinct from the main foiditic-phonolitic association of Mt. Vulture. We propose a petrogenetic/geodynamic interpretation which has important implications for understanding the relationships between carbonatites and orogenic activity. In particular, we propose that the studied alvikites are generated through liquid unmixing at crustal levels, starting from nephelinitic or melilititic parent liquids. These latter were produced in a hybrid mantle resulting from the interaction through a vertical slab window, between a metasomatized mantle wedge, moving eastward from the Tyrrhenian/Campanian region, and the local Adriatic mantle. The occurrence of carbonatite rocks at Mt. Vulture, that lies on the leading edge of the Southern Apennines accretionary prism, is taken as an evidence for the carbonatation of the mantle sources of this volcano. We speculate that mantle carbonatation is related to the introduction of sedimentary carbon from the Adriatic lithosphere during Tertiary subduction.     

Mid-Holocene to present-day evolution of the Indian monsoon in transient global simulations

The low-frequency evolution of Indian rainfall mean-state and associated interannual-to-decadal variability is discussed for the last 6000 years from a multi-configuration ensemble of fully coupled global transient simulations. This period is marked by a shift of Indian Summer Monsoon Rainfall (ISMR) distribution towards drier conditions, including extremes, and a contraction of the rainy season. The drying is larger in simulations with higher horizontal resolution of the atmosphere and revised land surface hydrology. Vegetation–climate interactions and the way runoff is routed to ocean modulate the timing of the monsoon onset but have negligible effects on the evolution of seasonal rainfall amounts in our modeling framework in which carbon cycling is always active. This drying trend is accompanied by changes in ISMR interannual-to-decadal variability decreasing over north and south India but increasing over central India (20°–25° N). The ISMR interannual-to-decadal variability is decomposed into six physically consistent regimes using a clustering technique to further characterize its changes and associated teleconnections. From 6 to 3.8 kyr bp, the century-to-century modulations in the frequency of occurrence associated to the regimes are asynchronous between the simulations. Orbitally-driven trends can only be detected for two regimes over the whole 6–0 kyr bp period. These two regimes reflect increased influence of ENSO on both ISMR and Indian Ocean Dipole as the inter-hemispheric energy gradient weakens. Severe long-term droughts are also shown to be a combination of long-term drying and internally generated low-frequency modulations of the interannual-to-decadal variability.

     

Geochronological data on recent magmatism of the Aegean Sea

Radiometric ages and chemical character of the Tertiary and Quaternary volcanics of the Aegean Sea indicate a gap between the Recent calc-alkaline volcanism and the Tertiary one. This latter reached its climax in the Oligocene—Late Miocene. The two calc-alkaline magmatisms are related to distinct subduction processes.     

Neogene and quaternary volcanism of the Bijar Area (Western Iran)

In the Bijar region (Western Iran) two distinct volcanic cycles have been recognized. The first, of Upper Miocene age, consists of high-K cale-alkaline volcanic rocks interpreted as final products of the cale-alkaline Tertiary phase of central Iran. The second volcanic cycle, mostly of Pleistocene age (0.5–1.3 m.v.) consists of undersaturated, mainly potassic, alkaline products. As the lavas of this last phase are slightly fractionated, the chemical differences shown by these rocks have been interpreted as primitive features related to the physical conditions governing the partial melting in the mantle and/or the mantle heterogeneity. In a volcanic center (Sarajukh volcano) contemporaneous basic and acid magmas have been found, and interpreted as derived from two different and independent sources. The alkaline basic volcanism is considered as an expression of disjunctive processes that have affected the western margin of the Iranian plate after the Pliocene.     

The Calabrian Stage redefined

The name Calabrian was introduced in the geological literature by the French stratigrapher Maurice Gignoux in 1910, and later described in his important monograph （633 pages） ＂Les formations marines pliocknes et quaternaires de l＇ltalie du sud et de la Sicile ＂published in 1913. Detailed data were provided on several sections （Santa Maria di Catanzaro, Caraffa, Monasterace, Palermo） and on their fossil content. The Calabrian Stage has commonly been used for over fifty years as the oldest subdivision of the Qua- ternary, notably in the time scales of Berggren ＆ van Cou- vering （1974） and Haq ＆ Eysinga （1987）. However, after the GSSP for the Pliocene/Pleistocene boundary （P/P） was approved by INQUA in 1982 and ratified by lUGS in 1984 at the Vrica section of Calabria, there was a decline in the usage of the stage name, and an increasing tendency by many Quaternary workers to question the boundary stratotype. This was because there was increasing evidence that it did not correspond to the beginning of the ＂ice age＂. In doing so, they were not complying with the recommendations presented at the 18th International Geological Congress （IGC） in London, 1948 （Oakley, 1950）.     

An instrument for commissioning the active and adaptive optics of modern telescopes: the Infrared Test Camera for the Large Binocular Telescope

We describe the design, integration, and operation of the infrared test cameras for the commissioning of the Large Binocular Telescope. The design and construction phase lasted slightly more than one year from February 2007 to April 2008 and was the result of a joint collaboration among INAF Osservatorio Astronomico di Bologna, Università di Bologna Dipartimento di Astronomia (Italy) and the Max-Planck-Institut für Astronomie (Heidelberg, Germany). Thereafter, the camera was delivered to the LBT Observatory (USA) for commissioning of the telescope active optics and, more recently, for commissioning of the first light adaptive optics.     

Helium and metal diffusion in the Sun and in cluster stars

In this contribution I will review the present knowledge about helium and metal diffusion efficiency in the Sun and in old cluster stars and the influence of the uncertainties still present on these mechanisms concerning the stellar characteristics in different evolutionary phases. I will also discuss the relevance of the current uncertainties on the assumed chemical composition for the main evolutionary features of population II stars.     

Thermal expansion and high-temperature P21/c–C2/c phase transition in clinopyroxene-type LiFeGe2O6 and comparison to NaFe(Si,Ge)2O6

A synthetic clinopyroxene with composition LiFe³⁺Ge₂O₆, monoclinic s.g. P2₁/c, a = 9.8792(7), b = 8.8095(5), c = 5.3754(3) Å, β = 108.844(6)°, V = 442.75(16) ų, has been studied by in situ low- and high-temperature single-crystal X-ray diffraction. The variation of lattice parameters and the intensity of the b-type reflections (h + k = 2n + 1, only present in the P-symmetry) with increasing temperature showed a displacive phase transition from space group P2₁/c to C2/c at a transition temperature T _tr = 789 K, first order in character, with a sudden volume increase of 1.6% and a decrease of β by 1° at the transition. This spontaneous dilatation is reversible, shows a limited hysteresis of ±10°C, and corresponds to the vanishing of the b-type reflections, thus indicating a symmetry increase to space group C2/c. Below T _tr an expansion is observed for all the cell parameters, while the β angle remained almost constant; at T > T _tr the thermal volume expansion is due to dilatation of the structure in the $(\bar{1}\,0\,1) A synthetic clinopyroxene with composition LiFe³⁺Ge₂O₆, monoclinic s.g. P2₁/c, a = 9.8792(7), b = 8.8095(5), c = 5.3754(3) ?, β = 108.844(6)°, V = 442.75(16) ?³, has been studied by in situ low- and high-temperature single-crystal X-ray diffraction. The variation of lattice parameters and the intensity of the b-type reflections (h + k = 2n + 1, only present in the P-symmetry) with increasing temperature showed a displacive phase transition from space group P2₁/c to C2/c at a transition temperature T _tr = 789 K, first order in character, with a sudden volume increase of 1.6% and a decrease of β by 1° at the transition. This spontaneous dilatation is reversible, shows a limited hysteresis of ±10°C, and corresponds to the vanishing of the b-type reflections, thus indicating a symmetry increase to space group C2/c. Below T _tr an expansion is observed for all the cell parameters, while the β angle remained almost constant; at T > T _tr the thermal volume expansion is due to dilatation of the structure in the ([`1] 0 1)(\bar{1}\,0\,1) plane, mostly along [0 1 0], and pure shear in the (0 1 0) plane due to the decrease of β. From comparison with silicate analogues, the germanate clinopyroxenes are more expansible, while the P2₁/c expands more than the C2/c phase. The evolution of Q ² (calculated as the normalized intensity of b-type reflections) with T in the framework of the Landau theory has been done using a standard expression for a first order phase transition. We observe a jump of Q ₀² = 0.538(2) at T _tr, with T _c of 481(7) K, b/a = −2,290 K, and c/a = 3,192 K, and thus far from being tri-critical point. A closely related composition (LiFe³⁺Si₂O₆) shows an equivalent phase transition at 228 K, which is very close to the tri-critical point and 561 K cooler. This result indicates that a change in the composition of tetrahedral sites can have dramatic effects on the P2₁/c ↔ C2/c displacive phase transition in clinopyroxenes. The major changes observed in the evolution of the crystal structure with T are observed in the M2 polyhedron, with a volume decrease by ca. 13.3%, compared to ca. 1.3% observed in the M1 polyhedron. The tetrahedra behave as rigid units with neither a significant change of volume at T > T _tr (<1‰), nor a change of tilting of the basal plane. No change in coordination is observed at T > T _tr in the M2 polyhedron, which remains sixfold coordinated although a strong deformation of this polyhedron is observed. This deformation is related to a strong change by 51.4° at T _tr of the kinking angle (O3–O3–O3 angle) of the B-chain of tetrahedra, which switches from O-rotated to S-rotated [from 143.3(5)° to 194.7(6)°]. The A-chain is S-rotated at T < T _tr [206.8(5)° at 703 K] and extends by 12° at the transition.     

A Fe K-edge XAS study of amethyst

An X-ray absorption spectroscopy (XAS) study of the Fe local environment in natural amethyst (a variety of α-quartz, SiO₂) has been carried out. Room temperature measurements were performed at the Fe K-edge (7,112 eV), at both the X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) regions. Experimental results were then compared with DFT calculations. XANES experimental spectra suggest Fe to occur mainly in the trivalent state, although a fraction of Fe²⁺ is identified. EXAFS spectra, on the other hand, reveal an unusual short distance for the first coordination shell:  = 1.78(2) Å, the coordination number being 2.7(5). These results allow to establish that Fe replaces Si in its tetrahedral site, and that numerous local distortions are occurring as a consequence of the presence of Fe³⁺ variably compensated by protons and/or alkaline ions, or uncompensated. The formal valence of Fe, on the basis of both experimental and DFT structural features, can be either 4+ or 3+. Taking into account the XANES evidences, we suggest that Fe mainly occurs in the trivalent state, compensated by protons, and that a minor fraction of Fe⁴⁺ is stabilised by the favourable local structural arrangement.     

A roadmap for a dedicated Earth Science Grid platform

Due to its intensive data processing and highly distributed organization, the multidisciplinary Earth Science applications community is uniquely positioned for the uptake and exploitation of Grid technologies. Currently Enabling Grids for E-sciencE, and other large Grid infrastructures are already deployed and capable of operational services. So far however, the adoption and exploitation of Grid technology throughout the Earth Science community has been slower than expected. The Dissemination and Exploitation of GRids in Earth sciencE project, proposed by the European Commission to assist and accelerate this process in a number of different ways, had between its main goals the creation of a roadmap towards Earth Science Grid platform. This paper presents the resulting roadmap.