An explosive component in a December 2020 Milan earthquake suggests outgassing of deeply recycled carbon

Carbon dragged at sub-arc depths and sequestered in the asthenospheric upper mantle during cold subduction is potentially released after millions of years during the breakup of continental plates. However, it is unclear whether these deep-carbon reservoirs can be locally remobilized on shorter-term timescales. Here we reveal the fate of carbon released during cold subduction by analyzing an anomalously deep earthquake in December 2020 in the lithospheric mantle beneath Milan (Italy), above a deep-carbon reservoir previously imaged in the mantle wedge by geophysical methods. We show that the earthquake source moment tensor includes a major explosive component that we ascribe to carbon-rich melt/fluid migration along upper-mantle shear zones and rapid release of about 17,000 tons of carbon dioxide when ascending melts exit the carbonate stability field. Our results underline the importance of carbon-rich melts at active continental margins for emission budgets and suggest their potential episodic contributions to atmospheric carbon dioxide.

Petrology of Mafic Dykes from the Njimom Area (West-Cameroon): A Contribution to the Characterization of Late Paleozoic and Mesozoic Magmatism in the Southern Continental Part of the Cameroon Volcanic Line

In the western Cameroon, crop out several dyke swarms of Paleozoic–Mesozoic age. These dykes intrude the Precambrian basement in the southern continental part of the Cretaceous Cameroon Volcanic Line. In the Njimom area, two groups of mafic dykes that crosscut the Neoproterozoic basement rocks have been observed. A first group intrudes the mylonites whereas the second group intrudes the granites. The dykes are alkaline basalts and hawaiites. The mineralogical assemblage of both groups of dykes consists of plagioclase, clinopyroxene, altered olivine, and opaque oxides. The dykes that cross-cut the Precambrian mylonitic gneisses show moderate TiO2 (1.7–2.0 wt.%), low MgO (4.4–7.1 wt.%), and compatible trace element concentrations (e.g., Cr = 70–180 ppm; Ni = 30–110 ppm). The dykes that intrude the granites have TiO2 contents between 2.3 and 2.5 wt.% and moderate compatible trace element concentrations (e.g., Cr = 260–280 ppm; Ni = 170–230 ppm). MgO varies from 5.9 to 9.2 wt.%. All mafic dykes are enriched in light lanthanide element and show moderate Zr/Nb and high Zr/Y, Nb/Yb, and Ti/V ratios similar to those of average ocean island basalt (OIB)-type magmas. Some dykes that intrude the mylonites show evidence of contamination by continental crust. The composition of the clinopyroxenes of the dykes that intrude the mylonites clearly indicate different and unrelated parental magmas from dykes that intrude the granites. Contents and fractionation of the least and the most incompatible elements suggest low degrees of partial melting (3–5%) of heterogeneous source slightly enriched in incompatible elements in the spinel stability field. The geochemical features of Njimom dykes (in particular the dykes that intrude the granites) are similar to those of Paleozoic and Mesozoic dykes recorded in the southern continental part of the Cameroon Volcanic Line, suggesting multiple reactivations of pre-existing fractures that resulted in the fragmentation of western Gondwana and the opening of the South Atlantic Ocean.

Unconventional Stoichiometries of Na–O Compounds at High Pressures

It has been realized that the stoichiometries of compounds may change under high pressure, which is crucial in the discovery of novel materials. This work uses systematic structure exploration and first-principles calculations to consider the stability of different stoichiometries of Na–O compounds with respect to pressure and, thus, construct a high-pressure stability field and convex hull diagram. Four previously unknown stoichiometries (NaO5, NaO4, Na4O, and Na3O) are predicted to be thermodynamically stable. Four new phases (P2/m and Cmc21 NaO2 and Immm and C2/m NaO3) of known stoichiometries are also found. The O-rich stoichiometries show the remarkable features of all the O atoms existing as quasimolecular O2 units and being metallic. Calculations of the O–O bond lengths and Bader charges are used to explore the electronic properties and chemical bonding of the O-rich compounds. The Na-rich compounds stabilized at extreme pressures (P > 200 GPa) are electrides with strong interstitial electron localization. The C2/c phase of Na3O is found to be a zero-dimensional electride with an insulating character. The Cmca phase of Na4O is a one-dimensional metallic electride. These findings of new compounds with unusual chemistry might stimulate future experimental and theoretical investigations.

Polybaric fractional crystallisation of arc magmas: an experimental study simulating trans-crustal magmatic systems

Crystallisation-driven differentiation is one fundamental mechanism proposed to control the compositional evolution of magmas. In this experimental study, we simulated polybaric fractional crystallisation of mantle-derived arc magmas. Various pressure–temperature trajectories were explored to cover a range of potential magma ascent paths and to investigate the role of decompression on phase equilibria and liquid lines of descent (LLD). Fractional crystallisation was approached in a step-wise manner by repetitively synthesising new starting materials chemically corresponding to liquids formed in previous runs. Experiments were performed at temperatures ranging from 1140 to 870 °C with 30 °C steps, and pressure was varied between 0.8 and 0.2 GPa with 0.2 GPa steps. For most fractionation paths, oxygen fugacity (fO2) was buffered close to the Ni-NiO equilibrium (NNO). An additional fractionation series was conducted at fO2 corresponding to the Re-ReO2 buffer (RRO ≈ NNO+2). High-pressure experiments (0.4–0.8 GPa) were run in piston cylinder apparatus while 0.2 GPa runs were conducted in externally heated pressure vessels. Resulting liquid lines of descent follow calc-alkaline differentiation trends where the onset of pronounced silica enrichment coincides with the saturation of amphibole and/or Fe–Ti–oxide. Both pressure and fO2 exert crucial control on the stability fields of olivine, pyroxene, amphibole, plagioclase, and Fe–Ti–oxide phases and on the differentiation behaviour of arc magmas. Key observations are a shift of the olivine–clinopyroxene cotectic towards more clinopyroxene-rich liquid composition, an expansion of the plagioclase stability field and a decrease of amphibole stability with decreasing pressure. Decompression-dominated ascent trajectories result in liquid lines of descent approaching the metaluminous compositional range observed for typical arc volcanic rocks, while differentiation trends obtained for cooling-dominated trajectories evolve to peraluminous compositions, similar to isobaric liquid lines of descent at elevated pressures. Experiments buffered at RRO provide a closer match with natural calc-alkaline differentiation trends compared to fO2 conditions close to NNO. We conclude that decompression-dominated fractionation at oxidising conditions represents one possible scenario for arc magma differentiation.

Shallow depth, substantial change: fluid-metasomatism causes major compositional modifications of subducted volcanics (Mariana forearc)

Mass transfer at shallow subduction levels and its ramifications for deeper processes remain incompletely constrained. New insights are provided by ocean island basalt (OIB) clasts from the Mariana forearc that experienced subduction to up to ~25–30 km depth and up to blueschist-facies metamorphism; thereafter, the clasts were recycled to the forearc seafloor via serpentinite mud volcanism. We demonstrate that the rocks were, in addition, strongly metasomatized: they exhibit K2O contents (median = 4.6 wt.%) and loss on ignition (median = 5.3 wt%, as a proxy for H2O) much higher than OIB situated on the Pacific Plate, implying that these were added during subduction. This interpretation is consistent with abundant phengite in the samples. Mass balance calculations further reveal variable gains in SiO2 for all samples, and MgO and Na2O increases at one but the loss of MgO and Fe2O3* at the other study site. Elevated Cs and Rb concentrations suggest an uptake whereas low Ba and Sr contents indicate the removal of trace elements throughout all clasts.The metasomatism was likely induced by the OIBs’ interaction with K-rich fluids in the subduction channel. Our thermodynamic models imply that such fluids are released from subducted sediments and altered igneous crust at 5 kbar and even below 200°C. Equilibrium assemblage diagrams show that the stability field of phengite significantly increases with the metasomatism and that, relative to not-metasomatized OIB, up to four times as much phengite may form in the metasomatized rocks. Phengite in turn is considered as an important carrier for K2O, H2O, and fluid-mobile elements to sub-arc depths.These findings demonstrate that mass transfer from subducting lithosphere starts at low P/T conditions. The liberation of solute-rich fluids can evoke far-reaching compositional and mineralogical changes in rocks that interact with these fluids. Processes at shallow depths (<30 km) thereby contribute to controlling which components as well as in which state (i.e., bound in which minerals) these components ultimately reach greater depths where they may or may not contribute to arc magmatism. For a holistic understanding of deep geochemical cycling, metasomatism and rock transformation need to be acknowledged from shallow depths on.

The forest ranger (and the legislator): How local congressional politics shape policy implementation in agency field offices

Research on political control over government bureaucracy has primarily focused on direct exercises of power such as appointments, funding, agency design, and procedural rules. In this analysis we extend this literature to consider politicians who leverage their institutional standing to influence the decisions of local field officials over whom they have no explicit authority. Using the case of the U.S. Forest Service (USFS), we investigate whether field-level decisions are associated with the political preferences of individual congressional representatives. Our sample encompasses 7,681 resource extraction actions initiated and analyzed by 107 USFS field offices between 2005 and 2018. Using hierarchical Bayesian regression, we show that under periods of economic growth and stability, field offices situated in the districts of congressional representatives who oppose environmental regulation initiate more extractive actions (timber harvest, oil and gas drilling, grazing) and conduct less rigorous environmental reviews than field offices in the districts of representatives who favor environmental regulation. By extending existing theories about interactions between politicians and bureaucrats to consider informal means of influence, this work speaks to: (1) the role of local political interests in shaping agency-wide policy outcomes; and (2) the importance of considering informal and implicit means of influence that operate in concert with explicit control mechanisms to shape bureaucratic behavior.

Defining the Structural Stability Field of Disordered Fluorite Oxides

Fluorite-structured oxides constitute an important class of materials for energy technologies. Despite their high level of structural symmetry and simplicity, these materials can accommodate atomic disorder without losing crystallinity, making them indispensable for uses in environments with high temperature, changing chemical compositions, or intense radiation fields. In this contribution, we present a set of simple rules that predict whether a compound may adopt a disordered fluorite structure. This approach is closely aligned with Pauling’s rules for ionic crystal structures and Goldschmidt’s rules for ionic substitution.

Periodically Released Magmatic Fluids Create a Texture of Unidirectional Solidification (UST) in Ore-Forming Granite: A Fluid and Melt Inclusion Study of W-Mo Forming Sannae-Eonyang Granite, Korea

The Upper Cretaceous Sannae-Eonyang granite crystallized approximately 73 Ma and hosted the Sannae W-Mo deposit in the west and the Eonyang amethyst deposit in the east. The granite contained textural zones of miarolitic cavities and unidirectional solidification texture (UST) quartz. The UST rock sampled in the Eonyang amethyst mine consisted of (1) early cavity-bearing aplitic granite, (2) co-crystallization of feldspars and quartz in a granophyric granite, and (3) the latest unidirectional growth of larger quartz crystals with clear zonation patterns. After the UST quartz was deposited, aplite or porphyritic granite was formed, repeating the prior sequence. Fluid and melt inclusions occurring in the UST quartz and quartz phenocrysts were sampled and studied to understand the magmatic-hydrothermal processes controlling UST formation and W-Mo mineralization in the granite. The composition of melt inclusions in the quartz phenocrysts suggested that the UST was formed by fractionated late-stage granite. Some of the melt inclusions occurring in the early-stage UST quartz were associated with aqueous inclusions, indicating fluid exsolution from a granitic melt. Hypersaline brine inclusions allowed the calculation of the minimum trapping pressure of 80–2300 bars. Such a highly fluctuating fluid pressure might be potentially due to a lithostatic-hydrostatic transition of pressure-attending fluid loss during UST formation. Highly fluctuating lithostatic-hydrostatic pressures created by fluid exsolution allowed shifting of the stability field from a quartz-feldspar cotectic to a single-phase quartz. The compositions of brine fluid assemblages hosted in the quartz phenocrysts deviated from the fluids trapped in the UST quartz, especially regarding the Rb/Sr and Fe/Mn ratios and W and Mo concentrations. The study of melt and fluid inclusions in the Eonyang UST sample showed that the exsolution of magmatic fluid was highly periodic. A single pulse of magmatic fluids of variable salinities/densities might have created a single UST sequence, and a new batch of magmatic fluid exsolution would be required to create the next UST sequence.

Synthetic and Natural Insecticides: Gas, Liquid, Gel and Solid Formulations for Stored-Product and Food-Industry Pest Control

The selective application of insecticides is one of the cornerstones of integrated pest management (IPM) and management strategies for pest resistance to insecticides. The present work provides a comprehensive overview of the traditional and new methods for the application of gas, liquid, gel, and solid physical insecticide formulations to control stored-product and food industry urban pests from the taxa Acarina, Blattodea, Coleoptera, Diptera, Hymenoptera, Lepidoptera, Psocoptera, and Zygentoma. Various definitions and concepts historically and currently used for various pesticide application formulations and methods are also described. This review demonstrates that new technological advances have sparked renewed research interest in the optimization of conventional methods such as insecticide aerosols, sprays, fumigants, and inert gases. Insect growth regulators/disruptors (IGRs/IGDs) are increasingly employed in baits, aerosols, residual treatments, and as spray-residual protectants for long-term stored-grain protection. Insecticide-impregnated hypoxic multilayer bags have been proven to be one of the most promising low-cost and safe methods for hermetic grain storage in developing countries. Insecticide-impregnated netting and food baits were originally developed for the control of urban/medical pests and have been recognized as an innovative technology for the protection of stored commodities. New biodegradable acaricide gel coatings and nets have been suggested for the protection of ham meat. Tablets and satchels represent a new approach for the application of botanicals. Many emerging technologies can be found in the form of impregnated protective packaging (insect growth regulators/disruptors (IGRs/IGDs), natural repellents), pheromone-based attracticides, electrostatic dust or sprays, nanoparticles, edible artificial sweeteners, hydrogels, inert baits with synthetic attractants, biodegradable encapsulations of active ingredients, and cyanogenic protective grain coatings. Smart pest control technologies based on RNA-based gene silencing compounds incorporated into food baits stand at the forefront of current strategic research. Inert gases and dust (diatomaceous earth) are positive examples of alternatives to synthetic pesticide products, for which methods of application and their integration with other methods have been proposed and implemented in practice. Although many promising laboratory studies have been conducted on the biological activity of natural botanical insecticides, published studies demonstrating their effective industrial field usage in grain stores and food production facilities are scarce. This review shows that the current problems associated with the application of some natural botanical insecticides (e.g., sorption, stability, field efficacy, and smell) to some extent echo problems that were frequently encountered and addressed almost 100 years ago during the transition from ancient to modern classical chemical pest control methods.