A recent theoretical study proposed that the anti-wear property of zinc dialkyl dithio phosphate (ZDDP) is due to the formation of chemically connected networks as a result of pressure-induced cross-linkage of phosphate groups of thermally decomposed ZDDP. To investigate the initial decomposition processes and the possibility of linking of phosphate groups in the decomposed product, in-situ high-pressure and high-temperature infrared (IR) spectroscopy using synchrotron radiation were performed on the original ZDDP. At room temperature no substantial structural change was observed up to 21.2 GPa, a pressure far exceeding the predicted onset of a structural transformation for the model zinc phosphate at 7 GPa. The observed Pressure induced broadening of the IR peaks is most likely associated with structural disorder or amorphization of ZDDP which is completely reversible upon decompression. When ZDDP is heated under pressure, an irreversible transformation was observed around 225 degrees C and 18.4 GPa. The experimental results show that ZDDP undergoes substantial decomposition at high pressures and high temperatures but no hint of cross-linkage of phosphate groups was found.

As the simplest stable boron hydride in its condensed phase, diborane exhibits an interesting structural chemistry with uniquely bridged hydrogen bonds. Here we report the first room-temperature infrared (IR) absorption spectra of solid diborane compressed to pressures as high as 50 GPa using a diamond anvil cell. At room temperature and 3.5 GPa, the IR spectrum of diborane displays rich sharply resolved fundamentals and overtones of the IR active bands, consistent with the previous low-temperature IR measurements of condensed diborane at ambient pressure. When compressed stepwise to 50 GPa, several structural transformations can be identified at pressures of similar to 3.5 GPa, similar to 6.9 GPa and similar to 14.7 GPa, as indicated by the changes in the band profile as well as the pressure dependence of the characteristic IR modes and bandwidths. These transformations can be interpreted as being enhanced intermolecular interactions resulting from compression. The geometry of the four-member ring of B(2)H(6), however, does not seem to be altered significantly during the transformations and the B(2)H(6) molecule remains chemically stable up to 50 GPa.

We report the structural transitions of pyridine as a function of pressure up to 26 GPa using in situ Raman spectroscopy and infrared absorption spectroscopy. By monitoring changes in the Raman shifts in the lattice region as well as the band profiles in both Raman and IR spectra, a liquid-to-solid transition at 1 GPa followed by solid-to-solid transitions at 2, 8, 11, and 16 GPa were observed upon compression. These transitions were found to be reversible upon decompression from 22 GPa. A further chemical transformation was observed when compressed beyond 22 GPa as evidenced by the substantial and irreversible changes in the Raman and infrared spectra, which could be attributed to the destruction of the ring structure. The observed transformations in pyridine were also compared to those for benzene. The similar transition sequence with well-aligned transition pressures suggests that these isoelectronic aromatics may have similar structures and stabilities under high pressure.

The size of nanocrystals provides a limitation on dislocation activity and associated stress-induced deformation. Dislocation-mediated plastic deformation is expected to become inactive below a critical particle size, which has been proposed to be between 10 and 30 nanometers according to computer simulations and transmission electron microscopy analysis. However, deformation experiments at high pressure on polycrystalline nickel suggest that dislocation activity is still operative in 3-nanometer crystals. Substantial texturing is observed at pressures above 3.0 gigapascals for 500-nanometer nickel and at greater than 11.0 gigapascals for 20-nanometer nickel. Surprisingly, texturing is also seen in 3-nanometer nickel when compressed above 18.5 gigapascals. The observations of pressure-promoted texturing indicate that under high external pressures, dislocation activity can be extended down to a few-nanometers-length scale.

Solar geoengineeringdeliberate reduction in the amount of solar radiation retained by the Earthhas been proposed as a means of counteracting some of the climatic effects of anthropogenic greenhouse gas emissions. We present results from Experiment G1 of the Geoengineering Model Intercomparison Project, in which 12 climate models have simulated the climate response to an abrupt quadrupling of CO2 from preindustrial concentrations brought into radiative balance via a globally uniform reduction in insolation. Models show this reduction largely offsets global mean surface temperature increases due to quadrupled CO2 concentrations and prevents 97% of the Arctic sea ice loss that would otherwise occur under high CO2 levels but, compared to the preindustrial climate, leaves the tropics cooler (-0.3K) and the poles warmer (+0.8K). Annual mean precipitation minus evaporation anomalies for G1 are less than 0.2mmday(-1) in magnitude over 92% of the globe, but some tropical regions receive less precipitation, in part due to increased moist static stability and suppression of convection. Global average net primary productivity increases by 120% in G1 over simulated preindustrial levels, primarily from CO2 fertilization, but also in part due to reduced plant heat stress compared to a high CO2 world with no geoengineering. All models show that uniform solar geoengineering in G1 cannot simultaneously return regional and global temperature and hydrologic cycle intensity to preindustrial levels.

It is well-believed that below a certain particle size, grain boundary-mediated plastic deformation (e. g., grain rotation, grain boundary sliding and diffusion) substitutes for conventional dislocation nucleation and motion as the dominant deformation mechanism. However, in situ probing of grain boundary processes of ultrafine nanocrystals during plastic deformation has not been feasible, precluding the direct exploration of the nanomechanics. Here we present the in situ texturing observation of bulk-sized platinum in a nickel pressure medium of various particle sizes from 500 nm down to 3 nm. Surprisingly, the texture strength of the same-sized platinum drops rapidly with decreasing grain size of the nickel medium, indicating that more active grain rotation occurs in the smaller nickel nanocrystals. Insight into these processes provides a better understanding of the plastic deformation of nanomaterials in a few-nanometer length scale.

We present the results of our analysis of the RR Lyrae (RRL) variable stars detected in two transition-type dwarf galaxies (dTrans), ESO294-G010 and ESO410-G005 in the Sculptor group, which is known to be one of the closest neighboring galaxy groups to our Local Group. Using deep archival images from the Advanced Camera for Surveys on board the Hubble Space Telescope, we have identified a sample of RRL candidates in both dTrans galaxies (219 RRab (RR0) and 13 RRc (RR1) variables in ESO294-G010; 225 RRab and 44 RRc stars in ESO410-G005). The metallicities of the individual RRab stars are calculated via the period-amplitude-[Fe/H] relation derived by Alcock et al. This yields mean metallicities of <[Fe/H]>(ESO294)=-1.77 +/- 0.03 and <[Fe/H]>(ESO410)=-1.64 +/- 0.03. The RRL metallicity distribution functions (MDFs) are investigated further via simple chemical evolution models; these reveal the relics of the early chemical enrichment processes for these two dTrans galaxies. In the case of both galaxies, the shapes of the RRL MDFs are well described by pre-enrichment models. This suggests two possible channels for the early chemical evolution for these Sculptor group dTrans galaxies: (1) the ancient stellar populations of our target dwarf galaxies might have formed from the star forming gas which was already enriched through "prompt initial enrichment" or an "initial nucleosynthetic spike" from the very first massive stars, or (2) this pre-enrichment state might have been achieved by the end products from more evolved systems of their nearest neighbor, NGC 55. We also study the environmental effects of the formation and evolution of our target dTrans galaxies by comparing their properties with those of 79 volume limited (D circle dot < 2Mpc) dwarf galaxy samples in terms of the luminosity-metallicity relation and the H I gas content. The presence of these RRL stars strongly supports the idea that although the Sculptor Group galaxies have a considerably different environment from the Local Group (e.g., no giant host galaxies, loosely bound and very low local density), they share a common epoch of early star formation with the dwarf satellite galaxies in the Local Group.

We present the first detailed study of the RR Lyrae variable population in the Local Group dSph/dIrr transition galaxy, Phoenix, using previously obtained HST/WFPC2 observations of the galaxy. We utilize template light curve fitting routines to obtain best fit light curves for RR Lyrae variables in Phoenix. Our technique has identified 78 highly probable RR Lyrae stars (54 ab-type; 24 c-type) with about 40 additional candidates. We find mean periods for the two populations of < P-ab >=0.60 +/- 0.03 days and < P-c >=0.353 +/- 0.002 days. We use the properties of these light curves to extract, among other things, a metallicity distribution function for ab-type RR Lyrae. Our analysis yields a mean metallicity of <[Fe/H]>=-1.68 +/- 0.06 dex for the RRab stars. From the mean period and metallicity calculated from the ab-type RR Lyrae, we conclude that Phoenix is more likely of intermediate Oosterhoff type; however the morphology of the Bailey diagram for Phoenix RR Lyraes appears similar to that of an Oosterhoff type I system. Using the RRab stars, we also study the chemical enrichment law for Phoenix. We find that our metallicity distribution is reasonably well fitted by a closed-box model. The parameters of this model are compatible with the findings of Hidalgo et al., further supporting the idea that Phoenix appears to have been chemically enriched as a closed-box-like system during the early stage of its formation and evolution.

The properties of satellite galaxies are closely related to their host galaxies in galaxy groups. In cluster environments, on the other hand, the interaction between close neighbors is known to be limited. Our goal is to examine the relationships between host and satellite galaxies in the harsh environment of a galaxy cluster. To achieve this goal, we study a galaxy cluster WHL J085910.0+294957 at z = 0.30 using deep images obtained with CQUEAN CCD camera mounted on the 2.1 m Otto Struve Telescope. After member selection based on the scaling relations of photometric and structural parameters, we investigate the relationship between bright (M-i <= -18) galaxies and their faint (-18 < M-i <= -15) companions. The weighted mean color of faint companion galaxies shows no significant dependence (< 1 sigma to bootstrap uncertainties) on cluster-centric distance and local luminosity density as well as the luminosity and concentration of an adjacent bright galaxy. However, the weighted mean color shows marginal dependence (similar to 2.2 sigma) on the color of an adjacent bright galaxy when the sample is limited to bright galaxies with at least two faint companions. By using a permutation test, we confirm that the correlation in color between bright galaxies and their faint companions in this cluster is statistically significant with a confidence level of 98.7%. The statistical significance increases if we additionally remove non-members using the Sloan Digital Sky Survey photometric redshift information (similar to 2.6 sigma and 99.3%). Our results suggest three possible scenarios: (1) vestiges of infallen groups, (2) dwarf capturing, and (3) tidal tearing of bright galaxies.

Global-scale solar geoengineering is the deliberate modification of the climate system to offset some amount of anthropogenic climate change by reducing the amount of incident solar radiation at the surface. These changes to the planetary energy budget result in differential regional climate effects. For the first time, we quantitatively evaluate the potential for regional disparities in a multi-model context using results from a model experiment that offsets the forcing from a quadrupling of CO2 via reduction in solar irradiance. We evaluate temperature and precipitation changes in 22 geographic regions spanning most of Earth's continental area. Moderate amounts of solar reduction (up to 85% of the amount that returns global mean temperatures to preindustrial levels) result in regional temperature values that are closer to preindustrial levels than an un-geoengineered, high CO2 world for all regions and all models. However, in all but one model, there is at least one region for which no amount of solar reduction can restore precipitation toward its preindustrial value. For most metrics considering simultaneous changes in both variables, temperature and precipitation values in all regions are closer to the preindustrial climate for a moderate amount of solar reduction than for no solar reduction.