On the statistical distribution of seismic velocities in Earth's deep mantle

The existence of uncoupled shear (S) and compression (P) wave velocity variations in Earth's mantle is a characteristic that might only be explained by the presence of significant chemical and/or phase heterogeneity, with important implications for the dynamics and evolution of Earth's interior. While making a one-to-one comparison between tomographic models for P and S velocity (V_P and V_S) variations for a particular geographic region is ill-posed, their global statistical distributions reveal several robust characteristics indicative of the nature of uncoupled V_P and V_S in the deep mantle. We find that all of the V_P and V_S model distributions at a given depth are Gaussian-like throughout the lowermost mantle. However, a distinct low velocity feature is present in V_S distributions below ≈ 2200 km depth that is not present or is relatively weak in V_P models. The presence of anomalously low V_S material cannot be explained as an artifact, nor can the absence of a similarly strong feature in P models be ascribed to under-resolution. We propose that this feature can be partly explained by laterally variable occurrences of post-perovskite (pPv) lenses in the D″ layer, however, the persistence of significantly slow V_S regions at heights up to ≈ 700 km or more above the core–mantle boundary is likely to be incompatible with a pPv origin and might only be explained by the presence of a laterally discontinuous layer of chemically distinct material and/or some other kind of phase heterogeneity. There also exist significant discrepancies between tomographic models with respect to the width of the distributions as well as differences between the modeled peak values. We propose a scheme for comparison between different seismic models in which the widths of the dominant features in their statistical distributions is exploited.     

Uniwavelength lidar sensitivity to spherical aerosol microphysical properties for the interpretation of Lagrangian stratospheric observations

The determination of stratospheric particle microphysical properties from multiwavelength lidar, including Rayleigh and/or Raman detection, has been widely investigated. However, most lidar systems are uniwavelength operating at 532 nm. Although the information content of such lidar data is too limited to allow the retrieval of the full size distribution, the coupling of two or more uniwavelength lidar measurements probing the same moving air parcel may provide some meaningful size information. Within the ORACLE-O3 IPY project, the coordination of several ground-based lidars and the CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation) space-borne lidar is planned during measurement campaigns called MATCH-PSC (Polar Stratospheric Clouds). While probing the same moving air masses, the evolution of the measured backscatter coefficient (BC) should reflect the variation of particles microphysical properties. A sensitivity study of 532 nm lidar particle backscatter to variations of particles size distribution parameters is carried out. For simplicity, the particles are assumed to be spherical (liquid) particles and the size distribution is represented with a unimodal log-normal distribution. Each of the four microphysical parameters (i.e. log-normal size distribution parameters, refractive index) are analysed separately, while the three others are remained set to constant reference values. Overall, the BC behaviour is not affected by the initial values taken as references. The total concentration (N₀) is the parameter to which BC is least sensitive, whereas it is most sensitive to the refractive index (m). A 2% variation of m induces a 15% variation of the lidar BC, while the uncertainty on the BC retrieval can also reach 15%. This result underlines the importance of having both an accurate lidar inversion method and a good knowledge of the temperature for size distribution retrieval techniques. The standard deviation (σ) is the second parameter to which BC is most sensitive to. Yet, the impact of m and σ on BC variations is limited by the realistic range of their variations. The mean radius (r_m) of the size distribution is thus the key parameter for BC, as it can vary several-fold. BC is most sensitive to the presence of large particles. The sensitivity of BC to r_m and σ variations increases when the initial size distributions are characterized by low r_m and large σ. This makes lidar more suitable to detect particles growing on background aerosols than on volcanic aerosols.     

Isotopic and geochemical characterization of salinization in the shallow aquifers of a reclaimed subsiding zone: The southern Venice Lagoon coastland

The coastal plain bordering the southern Venice Lagoon is a reclaimed lowland characterized by high subsidence rate, and ground level and water-table depth below sea level. In this agricultural region, where the surface hydrologic network is entirely artificially controlled by irrigation/drainage canals, salinization problems have long been encountered in soils and groundwaters. Here we use isotopic and geochemical tracers to improve our understanding of the origin of salinization and mineralization of the semi-confined aquifer (0–40 m), and the freshwater inputs to this hydrological system. Water samples have been collected at different seasons in the coastal Adriatic Sea, lagoon, rivers and irrigation canals, as well as in the semi-confined aquifer at depths between 12 and 35 m (14 boreholes), and in the first confined aquifer (three boreholes drilled between 40 and 80 m depth). Stable isotopes (δ¹⁸O and δD) and conductivity profiles show that direct saline intrusion from the sea or the lagoon is observed only in a restricted coastal strip, while brackish groundwaters are found over the entire topographic and piezometric depression in the centre of the study area. Fresh groundwaters are found only in the most western zone. The sharp isotopic contrast between the western and central regions suggests disconnected hydrological circulations between these two parts of the shallow aquifer. The border between these two regions also corresponds to the limits of the most strongly subsiding zone.Our results can be interpreted in terms of a four end-member mixing scheme, involving (1) marine water from the lagoon or the open sea, (2) alpine and pre-alpine regional recharge waters carried either by the main rivers Adige, Bacchiglione and Brenta (irrigation waters) or by the regional groundwater circulation, (3) local precipitation, and (4) evaporated waters infiltrated from the surface. Infiltration from the surface is also revealed by the stratification of the electrical conductivity profiles, showing that the brackish groundwaters are overlain by a shallow layer of less saline water all over the central depression. In the first confined aquifer, the groundwaters have isotopic compositions similar to the deep groundwaters of the Venetian confined aquifers (40–400 m depth). The isotopic data and the Br/Cl ratio show that the origin of the salinization of the phreatic aquifer can be ascribed to seawater intrusion alone, with no indication of the involvement of deep brines (identified at 450 m depth) in the process.The chemical composition of the saline and brackish groundwaters is characterized by an excess of sodium and a deficit of calcium compared to conservative mixing between fresh groundwaters and seawater. This suggests that the phreatic aquifer is progressively freshening, as a consequence of the beneficial influence of the extensive irrigation/drainage network, including raised canals acting as a hydraulic barrier along the coast. This freshening tendency may have been lasting since the reclamation in the mid-twentieth century, and has probably been accelerated by the ban on groundwater abstraction since the 1970s.     

Reforestation Programs in Southwest China： Reported Success, Observed Failure, and the Reasons Why

Ever since the disastrous floods of 1998, the Chinese government has used the Natural Forest Protection and Sloping Land Conversion Programs to promote afforestation and reforestation as means to reduce runoff, control erosion, and stabilize local livelihoods. These two ambitious programs have been reported as large-scale successes, contributing to an overall increase in China’s forest cover and to the stated goals of environmental stabilization. A small-scale field study at the project level of the implementation of these two programs in Baiwu Township, Yanyuan County, Sichuan, casts doubt upon the accuracy and reliability of these claims of success; ground observations revealed utter failure in some sites and only marginal success in others. Reasons for this discrepancy are posited as involving ecological, economic, and bureaucratic factors. Further research is suggested to determine whether these discrepancies are merely local aberrations or represent larger-scale failures in reforestation programs.     

Exploring the impact of diagenesis on (isotope) geochemical and microstructural alteration features in biogenic aragonite

For the Quaternary and Neogene, aragonitic biogenic and abiogenic carbonates are frequently exploited as archives of their environment. Conversely, pre‐Neogene aragonite is often diagenetically altered and calcite archives are studied instead. Nevertheless, the exact sequence of diagenetic processes and products is difficult to disclose from naturally altered material. Here, experiments were performed to understand biogenic aragonite alteration processes and products. Shell subsamples of the bivalve Arctica islandica were exposed to hydrothermal alteration. Thermal boundary conditions were set at 100°C, 175°C and 200°C. These comparably high temperatures were chosen to shorten experimental durations. Subsamples were exposed to different ¹⁸O‐depleted fluids for durations between two and twenty weeks. Alteration was documented using X‐ray diffraction, cathodoluminescence, fluorescence and scanning electron microscopy, as well as conventional and clumped isotope analyses. Experiments performed at 100°C show redistribution and darkening of organic matter, but lack evidence for diagenetic alteration, except in Δ₄₇ which show the effects of annealing processes. At 175°C, valves undergo significant aragonite to calcite transformation and neomorphism. The δ¹⁸O signature supports transformation via dissolution and reprecipitation, but isotopic exchange is limited by fluid migration through the subsamples. Individual growth increments in these subsamples exhibit bright orange luminescence. At 200°C, valves are fully transformed to calcite and exhibit purple‐blue luminescence with orange bands. The δ¹⁸O and Δ₄₇ signatures reveal exchange with the aqueous fluid, whereas δ¹³C remains unaltered in all experiments, indicating a carbonate‐buffered system. Clumped isotope temperatures in high‐temperature experiments show compositions in broad agreement with the measured temperature. Experimentally induced alteration patterns are comparable with individual features present in Pleistocene shells. This study represents a significant step towards sequential analysis of diagenetic features in biogenic aragonites and sheds light on reaction times and threshold limits. The limitations of a study restricted to a single test organism are acknowledged and call for refined follow‐up experiments.     

An Atomic Force Microscopy study of the growth of calcite in the presence of sodium sulfate

In situ atomic force microscopy (AFM) has been used to compare the growth of pure calcite and the growth of calcite in the presence of sulfate ions from aqueous solutions at a constant value of supersaturation (S.I. = 0.89) with respect to calcite. The effect of sulfate ions on calcite growth rates is determined and a potential incorporation of sulfate ions is identified in the calcite during growth. Solutions supersaturated with respect to calcite with solution concentration ratio of one and a constant pH of 10.2, were prepared and sulfate was added as Na₂SO₄ aqueous solution. The solution composition was readjusted in order to keep the supersaturation and pH constant. PHREEQC was used to determine relevant solution concentrations. In situ AFM experiments of calcite growth were performed using a fluid cell and flowing solutions passed over a freshly cleaved calcite surface. Growth rates were determined from the closure of the rhombohedral etch pits induced by initial dissolution with pure water. The spreading rate of 2-dimensional nuclei was also measured. At low concentrations of sulfate (≤ 0.5 mM), no effect on the growth rate of the calcite was observed. At higher concentrations (2 to 3 mM) of sulfate, the growth rate increased, possibly because a higher concentration of calcium and carbonate was necessary to maintain the supersaturation constant. At much higher concentrations of additional sulfate (up to 60 mM) the growth rate of the calcite was substantially decreased, despite the fact that a further increase of calcium and carbonate was required. The morphology of 2-dimensional growth nuclei became increasingly elongated with increasing sulfate content. Measurements of step height showed that newly grown steps were approximately 1 Å higher when grown in high sulfate concentrations, compared to steps grown in sulfate-free solutions. At sulfate concentrations above 5 mM the growth mechanism changes from layer growth to surface roughening. These observations suggest that the new growth has incorporated sulfate into the calcite surface.     

Northwest Africa 773: lunar mare breccia with a shallow-formed olivine-cumulate component, inferred very-low-Ti (VLT) heritage, and a KREEP connection

Lunar meteorite Northwest Africa 773 (herein referred to as NWA773) is a breccia composed predominantly of mafic volcanic components, including a prominent igneous clast lithology. The clast lithology is an olivine-gabbro cumulate, which, on the basis of mineral and bulk compositions, is a hypabyssal igneous rock related compositionally to volcanic components in the meteorite. The olivine-gabbro lithology exhibits cumulus textures and, in our largest section of it, includes some 48% olivine (Fo₆₄ to Fo₇₀, average Fo₆₇), 27% pigeonite (En₆₀Fs₂₄Wo₁₆ to En₆₇Fs₂₇Wo₆), 11% augite (En₅₀Fs₁₇Wo₃₃ to En₄₇Fs₁₃Wo₄₀), 2% orthopyroxene (En₇₀Fs₂₆Wo₄), 11% plagioclase (An₈₀ to An₉₄), and trace barian K-feldspar, ilmenite, Cr-spinel, RE-merrillite, troilite, and Fe-Ni metal. The Mg/Fe ratios of the mafic silicates indicate equilibration of Fe and Mg; however, the silicates retain compositional variations in minor and trace elements that are consistent with intercumulus crystallization. Accessory mineralogy reflects crystallization of late-stage residual melt. Both lithologies (breccia and olivine cumulate) of the meteorite have very-low-Ti (VLT) major-element compositions, but with an unusual trace-element signature compared to most lunar VLT volcanic compositions, i.e., relative enrichment in light REE and large-ion-lithophile elements, and greater depletion in Eu than almost all other known lunar volcanic rocks. The calculated composition of the melt that was in equilibrium with pyroxene and plagioclase of the cumulate lithology exhibits a KREEP-like REE pattern, but at lower concentrations. Melt of a composition calculated to have been in equilibrium with the cumulate assemblage, plus excess olivine, yields a major-element composition that is similar to known green volcanic glasses. One volcanic glass type from Apollo 14 in particular, green glass B, type 1, has a very low Ti concentration and REE characteristics, including extremely low Eu concentration, that make it a candidate parent melt for the olivine-gabbro cumulate. We infer an origin for the parent melt of NWA773 volcanic components by assimilation of a trace-element-rich partial or residual melt by a magnesian, VLT magma deep in the lunar crust or in the mantle prior to transportation to the near-surface, accumulation of olivine and pyroxene in a shallow chamber, eruption onto a volcanic surface, and incorporation of components into local, predominantly volcanic regolith, prior to impact mixing of the volcanic terrain and related hypabyssal setting, and ejection from the surface of the Moon. Volcanic components such as these probably occur in the Oceanus Procellarum region near the site of origin of the green volcanic glasses found in the Apollo 14 regolith.