We present a synthesis of PIXL elemental data and SHERLOC Raman spectra collected on two targets investigated by the Perseverance rover during the first year of its exploration of Jezero Crater, Mars. The Bellegarde target (in the M acute accent aaz formation) and Dourbes target (in the Se acute accent itah formation) exhibit distinctive mineralogies that are an ideal case study for in situ analysis by SHERLOC and PIXL. Each instrument alone produces valuable data about the chemistry and spatial distribution of mineral phases at the sub-millimeter scale. However, combining data from both instruments provides a more robust interpretation that overcomes the limitations of either instrument, for example: 1) Detection of correlated calcium and sulfur in Bellegarde by PIXL is corroborated by the co-located detection of calcium sulfate by SHERLOC. 2) Detection of sodium and chlorine in Dourbes is consistent with either chloride or oxychlorine salts, but SHERLOC does not detect perchlorate or chlorate. 3) A Raman peak at 1120 cm-1 in Dourbes could be sulfate or pyroxene, but elemental abundances from PIXL at that location are a better match to pyroxene. This study emphasizes the importance of analyzing co-located data from both instruments together, to obtain a more complete picture of sub-millimeter -scale mineralogy measured in situ in Jezero crater, Mars, by the Perseverance rover.

New data on the high-pressure melting curve of Ta up to 48 GPa are reported. Evidence of melting from changes in sample texture was found in five different experiments using scanning electron microscopy. The obtained melting temperatures are in excellent agreement with earlier measurements using X-ray diffraction or the laser-speckled method but are in contrast with several theoretical calculations. The results are also compared with shock-wave data. These findings are of geophysical relevance because they confirm the validity of earlier experimental techniques that resulted in low melting slopes of the transition metals measured in the diamond-anvil cell, including iron. (C) 2010 Elsevier B.V. All rights reserved.

A new method for measuring melting temperatures in the laser-heated diamond cell is described. This method circumvents previous problems associated with the sample instability, thermal runaway, and chemical reactions. Samples were heated with a single, 20 milliseconds rectangular pulse from a fiber laser, monitoring their thermal response with a fast photomultiplier while measuring the steady state temperature with a CCD spectrometer. The samples were recovered and analyzed using scanning electron microscopy. Focused ion beam milling allowed to examine both the lateral and the vertical solid-liquid boundaries. Ambient pressure tests reproducibly yielded the known melting temperatures of rhenium and molybdenum. Melting of Re was measured to 50 GPa, a 5-fold extension of previous data. The refractory character of Re is drastically enhanced by pressure, in contrast to Mo. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4730595]

The properties of solid and liquid phases of H2O at high pressure and temperature remain an active area of research. In this study, Brillouin spectroscopy has been used to determine the temperature dependence of sound velocities in H2O as a function of pressure up to 26 GPa through the phase field of ice VII and into the liquid to a maximum temperature of 1200 K. The Brillouin shift of the quasi-longitudinal acoustic mode moves to lower frequencies upon melting at each pressure. As a test of the method, measurements of the melting of Ar by Brillouin scattering at several pressures show a similar behavior for the acoustic mode, and measured melting points are consistent with previous results. The results of H2O melting are consistent with previously reported melting curves below 20 GPa. The data at higher pressure indicate that ice melts at a higher temperature than a number of previous studies have indicated.

Temperature, thermal history, and dynamics of Earth rely critically on the knowledge of the melting temperature of iron at the pressure conditions of the inner core boundary (ICB) where the geotherm crosses the melting curve. The literature on this subject is overwhelming, and no consensus has been reached, with a very large disagreement of the order of 2,000 K for the ICB temperature. Here we report new data on the melting temperature of iron in a laser-heated diamond anvil cell to 103 GPa obtained by X-ray absorption spectroscopy, a technique rarely used at such conditions. The modifications of the onset of the absorption spectra are used as a reliable melting criterion regardless of the solid phase from which the solid to liquid transition takes place. Our results show a melting temperature of iron in agreement with most previous studies up to 100 GPa, namely of 3,090 K at 103 GPa.

We demonstrate a new level of precision in measuring melting temperatures at high pressure using laser flash heating in a diamond cell followed by an analysis using scanning electron microscopy and focused ion beam milling. The new measurements on tantalum put unprecedented constraints on its highly debated melting slope, calling for a reevaluation of theoretical, shock compression, and diamond cell approaches to determine melting at high pressure. X-ray analysis of the recovered samples confirmed the absence of chemical reactions, which likely played a significant role in previous experiments.

Human emissions of CO2 now outpace natural sources by two orders of magnitude. The current concentration of CO2 has not been substantially exceeded in the past 30 million years. Multiple model exercises indicate that consuming all fossil fuels would result in concentrations more than double present levels, even after 10,000 years. The global warming effect of carbon emissions appears within 5-7 years. However, since the effect of present infrastructure over its expected life would only modestly increase CO2 concentrations and global temperature, human choices over its replacement will decisively influence ultimate carbon impacts, both short-term and long-term.

Global carbon emissions continue to acidify the oceans, motivating growing concern for the ability of coral reefs to maintain net positive calcification rates. Efforts to develop robust relationships between coral reef calcification and carbonate parameters such as aragonite saturation state ((arag)) aim to facilitate meaningful predictions of how reef calcification will change in the face of ocean acidification. Here we investigate natural trends in carbonate chemistry of a coral reef flat over diel cycles and relate these trends to benthic carbon fluxes by quantifying net community calcification and net community production. We find that, despite an apparent dependence of calcification on (arag) seen in a simple pairwise relationship, if the dependence of net calcification on net photosynthesis is accounted for, knowing (arag) does not add substantial explanatory value. This suggests that, over short time scales, the control of (arag) on net calcification is weak relative to factors governing net photosynthesis.

The Earth warms both when fossil fuel carbon is oxidized to carbon dioxide and when greenhouse effect of carbon dioxide inhibits longwave radiation from escaping to space. Various important time scales and ratios comparing these two climate forcings have not previously been quantified. For example, the global and time-integrated radiative forcing from burning a fossil fuel exceeds the heat released upon combustion within 2 months. Over the long lifetime of CO2 in the atmosphere, the cumulative CO2-radiative forcing exceeds the amount of energy released upon combustion by a factor >100,000. For a new power plant, the radiative forcing from the accumulation of released CO2 exceeds the direct thermal emissions in less than half a year. Furthermore, we show that the energy released from the combustion of fossil fuels is now about 1.71% of the radiative forcing from CO2 that has accumulated in the atmosphere as a consequence of historical fossil fuel combustion.

The climatic effects of Solar Radiation Management (SRM) geoengineering have been often modeled by simply reducing the solar constant. This is most likely valid only for space sunshades and not for atmosphere and surface based SRM methods. In this study, a global climate model is used to evaluate the differences in the climate response to SRM by uniform solar constant reduction and stratospheric aerosols. Our analysis shows that when global mean warming from a doubling of CO2 is nearly cancelled by both these methods, they are similar when important surface and tropospheric climate variables are considered. However, a difference of 1 K in the global mean stratospheric (61-9.8 hPa) temperature is simulated between the two SRM methods. Further, while the global mean surface diffuse radiation increases by similar to 23 % and direct radiation decreases by about 9 % in the case of sulphate aerosol SRM method, both direct and diffuse radiation decrease by similar fractional amounts (similar to 1.0 %) when solar constant is reduced. When CO2 fertilization effects from elevated CO2 concentration levels are removed, the contribution from shaded leaves to gross primary productivity (GPP) increases by 1.8 % in aerosol SRM because of increased diffuse light. However, this increase is almost offset by a 15.2 % decline in sunlit contribution due to reduced direct light. Overall both the SRM simulations show similar decrease in GPP (similar to 8 %) and net primary productivity (similar to 3 %). Based on our results we conclude that the climate states produced by a reduction in solar constant and addition of aerosols into the stratosphere can be considered almost similar except for two important aspects: stratospheric temperature change and the consequent implications for the dynamics and the chemistry of the stratosphere and the partitioning of direct versus diffuse radiation reaching the surface. Further, the likely dependence of global hydrological cycle response on aerosol particle size and the latitudinal and height distribution of aerosols is discussed.