On the iron isotope heterogeneity of lithospheric mantle xenoliths: implications for mantle metasomatism, the origin of basalts and the iron isotope composition of the Earth

With the aim to better understand the cause of the iron isotope heterogeneity of mantle-derived bulk peridotites, we compared the petrological, geochemical and iron isotope composition of four xenolith suites from different geodynamic settings; sub-arc mantle (Patagonia); subcontinental lithospheric mantle (Cameroon), oceanic mantle (Kerguelen) and cratonic mantle (South Africa). Although correlations were not easy to obtain and remain scattered because these rocks record successive geological events, those found between δ⁵⁷Fe, Mg#, some major and trace element contents of rocks and minerals highlight the processes responsible for the Fe isotope heterogeneity. While partial melting processes only account for moderate Fe isotope variations in the mantle (<0.2 ‰, with bulk rock values yielding a range of δ⁵⁷Fe ± 0.1 ‰ relative to IRMM-14), the main cause of Fe isotope heterogeneity is metasomatism (>0.9 ‰). The kinetic nature of rapid metasomatic exchanges between low viscosity melts/fluids and their wall-rocks peridotite in the mantle is the likely explanation for this large range. There are a variety of responses of Fe isotope signatures depending on the nature of the metasomatic processes, allowing for a more detailed study of metasomatism in the mantle with Fe isotopes. The current database on the iron isotope composition of peridotite xenoliths and mafic eruptive rocks highlights that most basalts have their main source deeper than the lithospheric mantle. Finally, it is concluded that due to a complex geological history, Fe isotope compositions of mantle xenoliths are too scattered to define a mean isotopic composition with enough accuracy to assess whether the bulk silicate Earth has a mean δ⁵⁷Fe that is chondritic, or if it is ~0.1 ‰ above chondrites as initially proposed.     

In situ investigations of allanite hydrothermal alteration: examples from calc-alkaline and anorogenic granites of Corsica (southeast France)

Allanite is, with monazite, the main repository for light rare earth elements (REE) in the continental crust and can be used in U-Th-Pb geochronology. This mineral has been shown to be prone to alteration. The geochemical exchanges occurring between allanite and hydrothermal fluids were explored using backscattered scanning electron microscopy, electron microprobe, and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The alteration mechanisms found show the restricted role of metamictization and correspond to the allanite to epidote transformation or to the leaching of the allanite A-crystallographic sites. Hence, the REE are mostly removed from this phase during fluid-mineral interactions, although a heavy rare earth-rich fluid may imprint its geochemical signature on the allanite altered zones. It appears that even if this REE holder presents evidence of alteration, the bulk mineral and whole-rock REE and Sm-Nd isotope signatures were not significantly affected in the cases studied. Alteration results mostly in the input of common lead, thus restricting the usefulness of allanite for U-Th-Pb dating when alteration occurs. Finally, the alteration mechanisms found here confirm the much more limited flexibility of silicates crystalline lattice as compared to phosphates.     

Contribution of long-term hydrothermal experiments for understanding the smectite-to-chlorite conversion in geological environments

The smectite-to-chlorite conversion is investigated through long-duration experiments (up to 9 years) conducted at 300 °C. The starting products were the Wyoming bentonite MX80 (79 % smectite), metallic iron and magnetite in contact with a Na–Ca chloride solution. The predominant minerals in the run products were an iron-rich chlorite (chamosite like) and interstratified clays interpreted to be chlorite/smectite and/or corrensite/smectite, accompanied by euhedral crystals of quartz, albite and zeolite. The formation of pure corrensite was not observed in the long-duration experiments. The conversion of smectite into chlorite over time appears to take place in several steps and through several successive mechanisms: a solid-state transformation, significant dissolution of the smectite and direct precipitation from the solution, which is over-saturated with respect to chlorite, allowing the formation of a chamosite-like mineral. The reaction mechanisms are confirmed by X-ray patterns and data obtained on the experimental solutions (pH, contents of Si, Mg, Na and Ca). Because of the availability of some nutrients in the solution, total dissolution of the starting smectite does not lead to 100 % crystallization of chlorite but to a mixture of two dominant clays: chamosite and interstratified chlorite/smectite and/or corrensite/smectite poor in smectite. The role of Fe/(Fe + Mg) in the experimental medium is highlighted by chemical data obtained on newly formed clay particles alongside previously published data. The newly formed iron-rich chlorite has the same composition as that predicted by the geothermometer for diagenetic to low-grade metamorphic conditions, and the quartz + Fe-chlorite + albite experimental assemblage in the 9-year experiment is close to that fixed by water–rock equilibrium.     

Trace element partitioning between carbonatitic melts and mantle transition zone minerals: Implications for the source of carbonatites

The occurrence of CO₂-rich lavas (carbonatites, kimberlites) and carbonate-rich xenoliths provide evidence for the existence of carbonatitic melts in the mantle. To model the chemical composition of such melts in the deep mantle, we experimentally determined partition coefficients for 23 trace elements (including REE, U-Th, HFSE, LILE) between deep mantle minerals and carbonatite liquids at 20 and 25 GPa and 1600 °C. Under these conditions, majoritic garnet and CaSiO₃ perovskite are the main reservoirs for trace elements. This study used both femtosecond LA-ICP-MS and SIMS techniques to measure reliable trace element concentrations. Comparison of the two techniques shows a general agreement, except for Sc and Ba. Our experimentally determined partition coefficients are consistent with the lattice strain model. The data suggest an effect of melt structure on partition coefficients in this pressure range. For instance, strain-free partition coefficient (D₀) for majorite-carbonatite melts do not follow the order of cation valence, , observed for majorite-CO₂-free silicate melts. The newly determined partition coefficients were combined with trace element composition of majoritic garnets found as inclusions in diamond to model trace element patterns of deep-seated carbonatites. The result compares favorably with natural carbonatites. This suggests that carbonatites can originate from the mantle transition zone.     

It starts at home? Climate policies targeting household consumption and behavioral decisions are key to low-carbon futures

Through their consumption behavior, households are responsible for 72% of global greenhouse gas emissions. Thus, they are key actors in reaching the 1.5 °C goal under the Paris Agreement. However, the possible contribution and position of households in climate policies is neither well understood, nor do households receive sufficiently high priority in current climate policy strategies. This paper investigates how behavioral change can achieve a substantial reduction in greenhouse gas emissions in European high-income countries. It uses theoretical thinking and some core results from the HOPE research project, which investigated household preferences for reducing emissions in four European cities in France, Germany, Norway and Sweden. The paper makes five major points: First, car and plane mobility, meat and dairy consumption, as well as heating are the most dominant components of household footprints. Second, household living situations (demographics, size of home) greatly influence the household potential to reduce their footprint, even more than country or city location. Third, household decisions can be sequential and temporally dynamic, shifting through different phases such as childhood, adulthood, and illness. Fourth, short term voluntary efforts will not be sufficient by themselves to reach the drastic reductions needed to achieve the 1.5 °C goal; instead, households need a regulatory framework supporting their behavioral changes. Fifth, there is a mismatch between the roles and responsibilities conveyed by current climate policies and household perceptions of responsibility. We then conclude with further recommendations for research and policy.     

Morphological controls on the dynamics of carbonate landscapes under a mediterranean climate

The influence of the morphological setting on the denudation of carbonate landscapes and the respective contributions of mechanical and chemical weathering processes are still debated. We have addressed these questions by measuring ³⁶Cl concentrations in 40 samples from the Luberon mountain, SE France, to constrain the denudation of various landscape elements. We observe a clear contrast between the local denudation rates from the flat summit surface, clustered around 30 mm/ka, and the basin‐average denudation rates across the flanks, ranging from 100 to 200 mm/ka. This difference highlights the transient evolution of the range, whose topography is still adjusting to previous uplift events. Such a pattern also suggests that carbonate dissolution is not the only driver of denudation in this setting, which appears to be significantly controlled by slope‐dependent processes.     

The March 25 and 29, 2016 landslide-induced debris flow at Clapar,Banjarnegara, Central Java

The Clapar landslide induced debris flow consisted of the Clapar landslide occurred on 24 March 2017 and the Clapar debris flow occurred on 29 March 2017. The first investigation of the Clapar landslide induced debris flow was carried out two months after the disaster. It was followed by UAV mapping, extensive interviews, newspaper compilation, visual observation and field measurements, and video analysis in order to understand chronology and triggering mechanism of the landslide induced debris flow in Clapar. The 24 March 2016 landslide occurred after 5 hours of consecutive rainfall (11,2 mm) and was affected by combination of fishponds leak and infiltration of antecedent rain. After five days of the Clapar landslide, landslide partially mobilized to form debris flow where the head scarp of debris flow was located at the foot of the 24 March 2016 landslide. The Clapar debris flow occurred when there was no rainfall. It was not generated by rainstorm or the surface erosion of the river bed, but rather by water infiltration through the crack formed on the toe of the 24 March 2016 landslide. Supply of water to the marine clay deposit might have increased pore water pressure and mobilized the soil layer above. The amount of water accumulated in the temporary pond at the main body of the 24 March 2016 landslide might have also triggered the Clapar debris flow. The area of Clapar landslide still shows the possibility of further retrogression of the landslide body which may induce another debris flow. Understanding precursory factors triggering landslides and debris flows in Banjarnegara based on data from monitoring systems and laboratory experiments is essential to minimize the risk of future landslide.     

Numerical modelling of circulation and dispersion processes in Boulogne-sur-Mer harbour (Eastern English Channel): sensitivity to physical forcing and harbour design

The MARS-3D model in conjunction with the particle tracking module Ichthyop is used to study circulation and tracer dynamics under a variety of forcing conditions in the eastern English Channel, and in the Boulogne-sur-Mer harbour (referred to hereafter as BLH). Results of hydrodynamic modelling are validated against the tidal gauge data, VHF radar surface velocities and ADCP measurements. Lagrangian tracking experiments are performed with passive particles to study tracer dispersal along the northern French coast, with special emphasis on the BLH. Simulations revealed an anticyclonic eddy generated in the harbour at rising tide. Tracers, released during flood tide at the Liane river mouth, move northward with powerful clockwise rotating current. After the high water, the current direction changes to westward, and tracers leave the harbour through the open boundary. During ebb tide, currents convergence along the western open boundary but no eddy is formed, surface currents inside the harbour are much weaker and the tracer excursion length is small. After the current reversal at low water, particles are advected shoreward resulting in a significant increase of the residence time of tracers released during ebb tide. The effect of wind on particle dispersion was found to be particularly strong. Under strong SW wind, the residence time of particles released during flood tide increases from 1.5 to 6 days. For release during ebb tide, SW wind weakens the southward tidally induced drift and thus the residence time decreases. Similar effects are observed when the freshwater inflow to the harbour is increased from 2 to 10 m³/s during the ebb tide flow. For flood tide conditions, the effect of freshwater inflow is less significant. We also demonstrate an example of innovative coastal management targeted at the reduction of the residence time of the pathogenic material accidentally released in the harbour.