Evaluating Competing Agent Strategies for a Voice Email Agent

This paper reports experimental results comparing a mixed-initiative to a system-initiative dialog strategy in the context of a personal voice email agent. To independently test the effects of dialog strategy and user expertise, users interact with either the system-initiative or the mixed-initiative agent to perform three successive tasks which are identical for both agents. We report performance comparisons across agent strategies as well as over tasks. This evaluation utilizes and tests the PARADISE evaluation framework, and discusses the performance function derivable from the experimental data.Comment: 6 pages latex, uses icassp91.sty, psfi

Estimation of pre-eruptive magmatic water fugacity in the Phlegrean Fields, Naples, Italy

International audienceWe estimated the water fugacity (fH(2)O) in the trachytic magma of Phlegrean Fields using the biotite-magnetite-sanidine equilibrium. We confirm that the partly ionic model is the most appropriate to estimate annite activity (a(annite)) for the experimental biotite. Crystallization experiments were carried out on a representative sample of trachytic Breccia Museo eruption, Naples, Italy. Experiments were performed in the temperature and pressure range or 725-870 degrees C and 50-200 MPa, and redox conditions ranging from NNO (nickel- nickel oxide) + 1 (+/- 0.2) to FMQ (fayalite + magnetite + quartz). Most experiments were done under conditions of H2O saturation (P-water = P-total). Few experiments were done using a mixed H2O-CO2 fluid phase. The pre-eruptive fH(2)O of the Phlegrean Fields magma is estimated at 735 bars, which compares well with available melt inclusion constraints. Our results confirm that this geohygrometer can be used in any magmatic systems bearing the worked assemblage

Identification of the first Rho–GEF inhibitor, TRIPα, which targets the RhoA-specific GEF domain of Trio

AbstractThe Rho–guanine nucleotide exchange factors (Rho–GEFs) remodel the actin cytoskeleton via their Rho–GTPase targets and affect numerous physiological processes such as transformation and cell motility. They are therefore attractive targets to design specific inhibitors that may have therapeutic applications. Trio contains two Rho–GEF domains, GEFD1 and GEFD2, which activate the Rac and RhoA pathways, respectively. Here we have used a genetic screen in yeast to select in vivo peptides coupled to thioredoxin, called aptamers, that could inhibit GEFD2 activity. One aptamer, TRIAPα (TRio Inhibitory APtamer), specifically blocks GEFD2-exchange activity on RhoA in vitro. The corresponding peptide sequence, TRIPα, inhibits TrioGEFD2-mediated activation of RhoA in intact cells and specifically reverts the neurite retraction phenotype induced by TrioGEFD2 in PC12 cells. Thus TRIPα is the first Rho–GEF inhibitor isolated so far, and represents an important step in the design of inhibitors for the expanding family of Rho–GEFs

Experimental partitioning of halogens and other trace elements between olivine, pyroxenes, amphibole and aqueous fluid at 2 GPa and 900–1,300 °C

We present new partition coefficients for various trace elements including Cl between olivine, pyroxenes, amphibole and coexisting chlorine-bearing aqueous fluid in a series of high-pressure experiments at 2 GPa between 900 and 1,300 °C in natural and synthetic systems. Diamond aggregates were added to the experimental capsule set-up in order to separate the fluid from the solid residue and enable in situ analysis of the quenched solute by LA–ICP–MS. The chlorine and fluorine contents in mantle minerals were measured by electron microprobe, and the nature of OH defects was investigated by infrared spectroscopy. Furthermore, a fluorine-rich olivine from one selected sample was investigated by TEM. Results reveal average Cl concentrations in olivine and pyroxenes around 20 ppm and up to 900 ppm F in olivine, making olivine an important repository of halogens in the mantle. Chlorine is always incompatible with Cl partition coefficients D Cl olivine/fluid varying between 10−5 and 10−3, whereas D Cl orthopyroxene/fluid and D Cl clinopyroxene/fluid are ~10−4 and D Cl amphibole/fluid is ~5 × 10−3. Furthermore, partitioning results for incompatible trace element show that compatibilities of trace elements are generally ordered as D amph/fluid ≈ D cpx/fluid > D opx/fluid > D ol/fluid but that D mineral/fluid for Li and P is very similar for all observed silicate phases. Infrared spectra of olivine synthesized in a F-free Ti-bearing system show absorption bands at 3,525 and ~3,570 cm−1. In F ± TiO2-bearing systems, additional absorption bands appear at ~3,535, ~3,595, 3,640 and 3,670 cm−1. Absorption bands at ~3,530 and ~3,570 cm−1, previously assigned to humite-like point defects, profit from low synthesis temperatures and the presence of F. The presence of planar defects could not be proved by TEM investigations, but dislocations in the olivine lattice were observed and are suggested to be an important site for halogen incorporation in olivine

Experimental cannibalization of plagioclase by alkaline basalt magmas

Time-series crystallization/dissolution experiments were conducted on a natural potassic basalt seeded with bytownitic plagioclases (Plg) at atmospheric pressure, in air, at 1180- 1240 °C and isothermal dwell time up to 20 hours. Plg-seed presence promotes the early formation of new-Plg, dampening the clinopyroxene (Cpx) crystallization. New-Plgs grow at a rate from 10-6 up to 10-8 cm·s-1 as the dwell time increases. Seeds overgrow at similar rate. Cpx crystallizes with a delay of at least 3 hours; this has a significant impact on the composition of both residual melt and new-Plgs. For undercooling >35 °C the Cpx delay causes a strong supersaturation of this phase in the melt resulting in a decrease in the new-Plg nucleation rate by 2 orders of magnitude in the 3 h-experiment. In the 15h-run, Cpx coarsening and the decrease of crystallinity suggest the achievement of a near-equilibrium conditions. Cpx growth rate is in the order of 10-7 cm·s-1 showing very limited variation. Finally, for the investigated superheating (5-15 °C) only the long lasting experiments allows an estimation of Plg dissolution rate (10-9 cm·s-1) although changes in the melt composition are already detectable in the 3h-runs. As a whole our results suggest that in natural systems, the takeover of antecrysts/ xenocrysts by a magma can induce on a short time scales, changes in its initial nucleation behavior with remarkable petrological implications for the solidification paths and eruptive dynamics of potassic magmatic systems

Crystallization Kinetics of Alkali Feldspar in Peralkaline Rhyolitic Melts: Implications for Pantelleria Volcano

Peralkaline rhyolites, associated with extensional tectonic settings, are medium to low viscosity magmas that often produce eruptive styles ranging from effusive to highly explosive eruptions. The role of pre-eruptive conditions and crystallization kinetics in influencing the eruptive style of peralkaline rhyolitic magmas has been investigated and debated considering equilibrium conditions. However, experimental constraints on the effect of disequilibrium in crystallization in such magmas are currently lacking in the literature. Therefore, we performed isobaric cooling experiments to investigate alkali feldspar crystallization kinetics in peralkaline rhyolitic melts. Experiments were performed under water-saturated, water-undersaturated, and anhydrous conditions between 25 and 100 MPa, at 670–790°C and with experimental durations ranging from 0.5 to 420 h. Here we present the first data on crystallization kinetics of alkali feldspar, which is the main crystal phase in peralkaline rhyolitic melts, in order to improve our understanding of the evolutionary timescales of these melts and their ability to shift between effusive and explosive activity. Our experimental results indicate that the alkali feldspar nucleation delay can range from hours to several days as a function of undercooling and H2O content in the melt. Thus, a peralkaline rhyolitic magma can be stored at the pre-eruptive conditions for days without important variations of its crystal fraction. This suggests that crystallization may not necessarily play the main role in triggering fragmentation during explosive eruptions of peralkaline rhyolitic magmas

Volatile and major element zonation within melt inclusions: A natural diffusion experiment

The diffusivities of volatile elements in silicate melts significantly impact petrological processes [e.g. 1, 2]. Although many studies of volatile diffusion in silicic melts have been undertaken, there have been few studies in basaltic melts [e.g. 3], and most of these have concentrated on the diffusion of only one or two elements in each experiment

The effect of diffusive re-equilibration time on trace element partitioning between alkali feldspar and trachytic melts

We present new experimental data on major and trace element partition coefficients between alkali feldspar and trachytic melt. Experiments were conducted at 500 MPa, 870 890 {\deg}C to investigate through short disequilibrium and long near equilibrium experiments the influence of diffusive re-equilibration on trace element partitioning during crystallization. Our data show that Ba and Sr behave compatibly, and their partition coefficients are influenced by re-equilibration time, orthoclase (Or) content, growth rate and cation order-disorder. High field strength elements (HFSE) and rare earth elements (except Eu) are strongly incompatible, but alkali feldspar efficiently fractionates light (LREE) from heavy rare earth elements (HREE). Our crystallization experiments reveal a strong influence of disequilibrium crystal growth on the partitioning of Ba and Sr. In particular, short-duration experiments show that rapid alkali feldspar crystal growth after nucleation, promotes disordered growth and less selectivity in the partitioning of compatible trace elements that easily enter the crystal lattice (e.g., Ba and Sr)...