具平缓电子能谱的伽玛射线暴的解析光变曲线

在标准的伽玛暴余辉模型中,电子通过费米一级加速后形成单幂律能谱分布dn/dγe∝γe-p(p≈2.3),但在某些伽玛暴事件中观测到了平缓的电子能谱分布(即p＜2).在单幂律谱和分段幂律谱两种情况下,分别给出了具有平缓电子能谱的伽玛暴余辉的解析光变曲线,并以GRB 060908为例进行了讨论.同时提出了伽玛暴低能谱危机的...     

Studying the SN‐GRB connection with X‐shooter: The GRB 100316D / SN 2010bh case

During the last ten years, observations of long‐duration gamma‐ray bursts brought to the conclusion that at least a fraction of them is associated with bright supernovae of type Ib/c. In this talk, after a short review on the previously observed GRB‐SN connection cases, we present the recent case of GRB 100316/SN 2010bh. In particular, during the observational campaign of SN 2010bh, a pivotal role was played by VLT/X‐shooter, sampling with unique high quality data the spectral energy distribution of the early evolution phases from the UV to the K band (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Supernovae interacting with a circumstellar medium: New observations with X‐shooter

In this article we present new data of a sample of core‐collapse supernovae showing unequivocal evidences of interaction between their ejecta and pre‐existing circumstellar matter (CSM). This CSM was produced by the progenitor star through major mass loss episodes during the final stages of its life. The study of the properties of the SN ejecta and the circumstellar environment are crucial to unveil the nature of the progenitors producing interacting supernovae. In this context, the instrumental combination Very Large Telescope (VLT) plus X‐shooter provides spectra covering simultaneously the optical and near‐infrared domains, and with adequate resolution to constrain the main properties of the supernova and its environment, including its chemical composition, the ejection velocity and the distribution of the emitting gas (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Dissociation Constants of Protonated Oxidized Glutathione in Seawater Media at Different Salinities

Oxidized glutathione (GSSG), which has four carboxylic and two amino groups, interacts with metal ions and may affect the bioavailability and geochemistry of metals in natural waters. In the present paper, six stepwise protonation constants K^\textH_i K^{\text{H}}_{i} for GSSG were measured as a function of salinity, S = 5–35‰ at t = 25°C (and in NaCl/MgCl₂ mixtures at different ionic strengths), in order to provide thermodynamic data for their acid base properties, which are useful for studying the interaction with metals in these media. The protonation enthalpies (ΔH _i /kJ mol⁻¹) were also determined at t = 25°C. The results were interpreted using the SIT model and Pitzer equations. The seawater model with the interaction parameters accounts for the differences between the values in NaCl and seawater. The results suggest that it is important to consider all of the ionic interactions in natural waters in examining the proton dissociation of GSSG.     

Hydrogeochemistry of Roccamonfina volcano (Southern Italy)

This is the first hydro-geochemical investigation carried out on the Roccamonfina Volcanic Complex groundwaters. The chemistry of Roccamonfina waters is defined by water–rock and water–rock–gas interactions. In fact, interactions between rocks of the first eruptive high-K formations and circulating groundwaters are recognized by high K concentrations. On the other hand, inverse concentration of calcium versus alkali metals is related to two different rock interactions occurring in different areas of the volcano: (a) within the caldera where groundwaters flow within latite and pyroclastic formations releasing calcium, and (b) similarly at the base of the volcano where groundwaters flowing from surrounding carbonates got strongly enriched in Ca. These geochemical processes are also associated with K (SE of caldera) and Mg/Ca (in sites located at the NE base of the volcano) decrease. Completely different dynamics occurs at Riardo groundwaters (SE). Here waters are the result of a mix between the Roccamonfina deep aquifer and the carbonate aquifer of the Riardo plain. Rich-CO₂ emissions make these waters strongly mineralized. Minor elements show a similar geochemical behavior of major ions and are crucial defining interactions processes. The evolution of Roccamonfina groundwaters is also evident along the simultaneous enrichment of Ba, Sr, and Ca. Ba increase is the result of deep local carbonate alteration enhanced by CO₂ emissions and, the lower Sr/Ca ratio, from 10 to 2 (ppb/ppm), is also due to the same process. In the light of our results the Roccamonfina aquifer can be schematically divided into two main reservoirs: (a) a superficial aquifer which basically follows the volcanic structure morphology and tectonics and (b) a deeper reservoir, originating within the oldest Roccamonfina volcano ultra potassic lavas and then flowing into the carbonate aquifers of the neighboring plain. Eventually, the chemistry of the Roccamonfina aquifer does not show any specific and visible pollution, contrary to what happens in the volcano surrounding plains. In fact, only 14% of the samples we collected (206) show a NO₃ content >30 mg/l. These sites are all located at the base of the volcano, near the plain.     

Determination of the relative thermal conductivity of solid samples by X-ray diffraction device

The thermal conductivity (TC) of metal and rock samples was determined, under ambient conditions, using standard X-ray diffraction equipment in which only the diffractometer sample holder had been modified from the original. As the method is comparative, standard reference materials were used: a copper standard for the analysis of metals and marble for the rock specimens. The marble was analyzed beforehand using a quick thermal conductivity meter QTM. In experimental measurements of TC the mean reproducibility value appears to be about 4% while the accuracy is about 5% for the examined rocks, and better for metals.     

In Situ Multi-Element Analysis of the Mount Pinatubo Quartz-Hosted Melt Inclusions by NIR Femtosecond Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry

Microscopic melt inclusions found in magmatic minerals are undoubtedly one of the most important sources of information on the chemical composition of melts. This paper reports on the successful application of near-infrared (NIR) femtosecond laser ablation (LA) - inductively coupled plasma-mass spectrometry to in situ determination of incompatible trace elements (Li, Rb, Sr, Y, Zr, Nb, Cs, Ba, REE, Ta, Th, U) and ore metals (As, Mo, Pb) in individual melt inclusions hosted in quartz from the Mount Pinatubo dacites, Philippines. The determined elements cover a concentration range of five orders of magnitude. Femtosecond LA-ICP-MS analyses of twenty-eight individual melt inclusions demonstrate the efficiency of the microanalytical technique and suggests a spectacular homogeneity of the entrapped melt, at least with respect to the following incompatible trace elements: Rb, Sr, Nb, Cs, Ba, La, Ce, Pr, Nd, Pb, Th. The analytical precision (1s) for Na, Ca, Rb, Sr, Y, Nb, Ba and LREE ranged from 3 to 20%. Comparison of trace element concentrations in Mt. Pinatubo melt inclusions determined by femtosecond LA-ICP-MS with those of melt inclusions previously analysed by secondary ion mass spectrometry analysis (SIMS) and those of matrix glasses previously determined by nanosecond LA-ICP-MS showed an agreement typically within 30–40%. The homogeneity of trace element concentrations of the Mt. Pinatubo melt inclusions and the matrix glasses is consistent with the melt inclusion origin as homogeneous rhyolitic melt that was trapped in quartz phenocrysts at the final crystallisation stages of the host adakite (dacite) magma.     

Magnetic fabric of Pleistocene continental clays from the hanging-wall of an active low-angle normal fault (Altotiberina Fault,Italy)

Anisotropy of magnetic susceptibility (AMS) represents a valuable proxy able to detect subtle strain effects in very weakly deformed sediments. In compressive tectonic settings, the magnetic lineation is commonly parallel to fold axes, thrust faults, and local bedding strike, while in extensional regimes, it is perpendicular to normal faults and parallel to bedding dip directions. The Altotiberina Fault (ATF) in the northern Apennines (Italy) is a Plio-Quaternary NNW–SSE low-angle normal fault; the sedimentary basin (Tiber basin) at its hanging-wall is infilled with a syn-tectonic, sandy-clayey continental succession. We measured the AMS of apparently undeformed sandy clays sampled at 12 sites within the Tiber basin. The anisotropy parameters suggest that a primary sedimentary fabric has been overprinted by an incipient tectonic fabric. The magnetic lineation is well developed at all sites, and at the sites from the western sector of the basin it is oriented sub-perpendicular to the trend of the ATF, suggesting that it may be related to extensional strain. Conversely, the magnetic lineation of the sites from the eastern sector has a prevailing N–S direction. The occurrence of triaxial to prolate AMS ellipsoids and sub-horizontal magnetic lineations suggests that a maximum horizontal shortening along an E–W direction occurred at these sites. The presence of compressive AMS features at the hanging-wall of the ATF can be explained by the presence of gently N–S-trending local folds (hardly visible in the field) formed by either passive accommodation above an undulated fault plane, or rollover mechanism along antithetic faults. The long-lasting debate on the extensional versus compressive Plio-Quaternary tectonics of the Apennines orogenic belt should now be revised taking into account the importance of compressive structures related to local effects.     

Eclogite-facies vein systems in the Marun-Keu complex (Polar Urals,Russia): textural,chemical and thermal constraints for patterns of fluid flow in the lower crust

Metasomatic amphibole-eclogite sequences grew in selvages of quartz veins from the Marun-Keu complex (Polar Urals, Russia) during high-pressure metamorphism. Relicts of a pre-metasomatic eclogite-facies assemblage are present in the wallrock layers as irregular patches. Wallrock interstitial quartz trails lying at a high angle to reaction fronts provide evidence for grain-scale pore channelisation which may be produced by intergranular-fluid compositional gradients parallel to the quartz trails. Disequilibrium at vein-wallrock scale is inferred from wallrock mineral heterogeneity and from variable initial Sr isotope ratios in mineral separates. Mass-balance calculations between relicts and wallrock assemblages reveal chemical imbalances caused by open system-behaviour with two way mass-transfer. The vein-wallrock system registers a prograde history from 408–434 °C (relicts) to 526–668 °C (vein precipitates). Vein and metasomatic assemblages formed during a single fluid-rock interaction process, implying high heating rates (100 °C/Ma), which could result from heat advection by large-scale fluid circulation.Editorial responsibility: W. Schreyer     

Enigmatic diamonds in Archean calc-alkaline lamprophyres of Wawa, southern Ontario, Canada

A suite of 80 macrodiamonds recovered from volcaniclastic breccia of Wawa (southern Ontario) was characterized on the basis of morphology, nitrogen content and aggregation, cathodoluminescence (CL), and mineral inclusions. The host calc-alkaline lamprophyric breccias were emplaced at 2.68–2.74 Ga, contemporaneously with voluminous bimodal volcanism of the Michipicoten greenstone belt. The studied suite of diamonds differs from the vast majority of diamond suites found worldwide. First, the suite is hosted by calc-alkaline lamprophyric volcanics rather than by kimberlite or lamproite. Second, the host volcanic rock is amongst the oldest known diamondiferous rocks on Earth, and has experienced regional metamorphism and deformation. Finally, most diamonds show yellow-orange-red CL and contain mineral inclusions not in equilibrium with each other or their host diamond. The majority of the diamonds in the Wawa suite are colorless, weakly resorbed, octahedral single crystals and aggregates. The diamonds contain 0–740 ppm N and show two modes of N aggregation at 0–30 and 60–95% B-centers suggesting mantle storage at 1,100–1,170°C. Cathodoluminescence and FTIR spectroscopy shows that emission peaks present in orange CL stones do not likely result from irradiation or single substitutional N, in contrast to other diamonds with red CL. The diamonds contain primary inclusions of olivine (Fo₉₂ and Fo₈₉), omphacite, orthopyroxene (En₉₃), pentlandite, albite, and An-rich plagioclase. These peridotitic and eclogitic minerals are commonly found within single diamonds in a mixed paragenesis which also combines shallow and deep phases. This apparent disequilibrium can be explained by effective small-scale mixing of subducted oceanic crust and mantle rocks in fast “cold” plumes ascending from the top of the slabs in convergent margins. Alternatively, the diamonds could have formed in the pre-2.7–2.9 Ga cratonic mantle and experienced subsequent alteration of syngenetic inclusions related to host magmatism and ensuing metamorphism. Neither orogenic nor cratonic model of the diamond origin fully explains all of the observed characteristics of the diamonds and their host rocks. Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.