Grain‐scale dependency of metamorphic reaction on crystal plastic strain

The Breaksea Orthogneiss in Fiordland, New Zealand preserves water‐poor intermediate and mafic igneous rocks that were partially recrystallized to omphacite granulite and eclogite, respectively, at P ≈ 1.8 GPa and T ≈ 850°C. Metamorphic reaction consumed plagioclase and produced grossular‐rich garnet, jadeite‐rich omphacite, clinozoisite and kyanite. The extent of metamorphic reaction, identified by major and trace element composition and microstructural features, is patchy on the grain and outcrop scale. Domains of re‐equilibration coincide with areas that exhibit higher strain suggesting a causal link between crystal plastic strain and metamorphic reaction. Quantitative orientation analysis (EBSD) identifies gradual and stepped changes in crystal lattice orientations of igneous phenocrysts that are surrounded by homophase areas of neoblasts, characterized by high grain boundary to volume ratios and little to no internal lattice distortion. The narrow, peripheral compositional modification of less deformed garnet and omphacite phenocrysts reflects limited lattice diffusion in areas that lacked three‐dimensional networks of interconnected low‐angle boundaries. Low‐angle boundaries acted as elemental pathways (pipe diffusion) that enhanced in‐grain element diffusion. The scale of pipe diffusion is pronounced in garnet relatively to clinopyroxene. Strain‐induced mineral transformation largely controlled the extent of high‐T metamorphic reaction under relatively fluid‐poor conditions.     

The field and microstructural signatures of deformation‐assisted melt transfer: Insights from magmatic arc lower crust,New Zealand

Melt must transfer through the lower crust, yet the field signatures and mechanisms involved in such transfer zones (excluding dykes) are still poorly understood. We report field and microstructural evidence of a deformation‐assisted melt transfer zone that developed in the lower crustal magmatic arc environment of Fiordland, New Zealand. A 30–40 m wide hornblende‐rich body comprising hornblende ± clinozoisite and/or garnet exhibits 'igneous‐like' features and is hosted within a metamorphic, two‐pyroxene–pargasite gabbroic gneiss (GG). Previous studies have interpreted the hornblende‐rich body as an igneous cumulate or a mass transfer zone. We present field and microstructural characteristics supporting the later and indicating the body has formed by deformation‐assisted, channelized, reactive porous melt flow. The host granulite facies GG contains distinctive rectilinear dykes and garnet reaction zones (GRZ) from earlier in the geological history; these form important reaction and strain markers. Field observations show that the mineral assemblages and microstructures of the GG and GRZ are progressively modified with proximity to the hornblende‐rich body. At the same time, GRZ bend systematically into the hornblende‐rich body on each side of the unit, showing apparent sinistral shearing. Within the hornblende‐rich body itself, microstructures and electron back‐scatter diffraction mapping show evidence of the former presence of melt including observations consistent with melt crystallization within pore spaces, elongate pseudomorphs of melt films along grain boundaries, minerals with low dihedral angles as small as <10° and up to <60°, and interconnected 3D melt pseudomorph networks. Reaction microstructures with highly irregular contact boundaries are observed at the field and thin‐section scale in remnant islands of original rock and replaced grains, respectively. We infer that the hornblende‐rich body was formed by modification of the host GG in situ due to reaction between an externally derived, reactive, hydrous gabbroic to intermediate melt percolating via porous melt flow through an actively deforming zone. Extensive melt–rock interaction and metasomatism occurred via coupled dissolution–precipitation, triggered by chemical disequilibrium between the host rock and the fluxing melt. As a result, the host plagioclase and pyroxene became unstable and were reacted and dissolved into the melt, while hornblende and to a lesser extent clinozoisite and garnet grew replacing the unstable phases. Our study shows that hornblendite rocks commonly observed within deep crustal sections, and attributed to cumulate fractionation processes, may instead delineate areas of deformation‐assisted, channelized reactive porous melt flow formed by melt‐mediated coupled dissolution–precipitation replacement reactions.     

Remote sensing-based assessment of tsunami vulnerability and risk in Alexandria, Egypt

Tsunamis can cause catastrophic loss of life, destruction of property, engineered structures and coastal infrastructure, and they can lead to major economic losses. Even though tsunamis are relatively rare in the Mediterranean Sea, their potential danger to cities along the Mediterranean coast cannot be neglected. In order to create awareness among the potentially affected people it is important to know the risk and vulnerability of the population and infrastructure related to a possible tsunami impact. In this work a hazard, vulnerability and risk analysis for buildings in two districts of Alexandria was carried out. Relevant input parameters were derived mainly from remote sensing and field data and were analyzed with a geographical information system (GIS). Based on historical records of past tsunamis, two inundation scenarios of 5 m and 9 m were defined and modeled applying a bath-type model. The resulting tsunami building risk zone maps showed that 12% of the buildings in El Gomrok district are at high or very high risk for the 5 m scenario, while the risk for El Montazah area is low. For the 9 m scenario, on the other hand, the majority of the buildings in both districts, 56% of El Gomrok, and 60% of El Montazah, are in the high or very high risk zone. An analysis of the building use indicated that the majority of these buildings are residential and commercial types, highlighting that the potential consequences of a tsunami could be severe. Due to the scarcity of historical data no frequency could be associated with the two selected scenarios. While both are credible we consider the 5 m scenario as possible but unlikely and the 9 m scenario as unlikely.     

Measurement of SIMS Instrumental Mass Fractionation of Pb Isotopes During Zircon Dating

An igneous zircon reference material (OG1) was characterised for U-Pb isotopes by ID-TIMS, and utilised to evaluate SIMS (SHRIMP) instrumental mass fractionation (IMF) of radiogenic Pb isotopes (²⁰⁷Pb*/²⁰⁶Pb*). The TIMS ²⁰⁷Pb*/²⁰⁶Pb* reference value for OG1 was 0.29907 ± 0.00011 (95% confidence limit), 3465.4 ± 0.6 Ma. The high ²⁰⁷Pb* (∼ 30 μg g⁻¹), negligible common Pb, and isotopic homogeneity permitted precise (± 1–2‰) ²⁰⁷Pb*/²⁰⁶Pb* measurements within the analytical sessions. External reproducibility of mean ²⁰⁷Pb*/²⁰⁶Pb* ratios between sessions was demonstrated for one instrument, yielding a mean IMF of +0.87 ± 0.49‰. The mean ²⁰⁷Pb*/²⁰⁶Pb* ratios between instruments were dispersed beyond uncertainties, with session IMF values from +3.6 ± 1.7‰ to −2.4 ± 1.3‰, and a grand mean IMF value (twenty-six sessions) of +0.70 ± 0.52‰, indicating a tendency towards elevated ²⁰⁷Pb*/²⁰⁶Pb*. The specific causes of variability in IMF are unclear, but generally reflect subtle differences in analytical conditions. The common practice in SIMS of assuming that IMF for Pb⁺ is insignificant could result in systematic age biases and underestimated uncertainties, of critical importance for precise correlation of Precambrian events. Nevertheless, a zircon RM such as OG1 can be readily incorporated into routine dating to improve ²⁰⁷Pb*/²⁰⁶Pb* accuracy and external reproducibility.     

Metal distribution in sediment cores from São Paulo State Coast, Brazil

Ten sediment core samples with lengths ranging from 35 to 100 cm were collected in the Baixada Santista region and analyzed to determine As, Br, Co, Cr, Cs, Fe, Rb, Sb, Ta, Th, U, Zn and rare earths (Sc, Ce, Eu, La, Lu, Nd, Sm, Tb and Yb) level concentrations using instrumental neutron activation analysis (INAA). The studied region is located in the southeastern coast of São Paulo State and is comprised of a densely urbanized area, the largest industrial complex of the country, with a predominance of petrochemical and fertilizer plants. It is also home to Brazil’s most important and busiest port. The conclusions found that the As, La, Sm, Ne, Ce, Eu, Hf, Ta, Th, and U elements have a high background level in the region and that Fe and Zn were the main indicators of anthropogenic contribution in the sediments.     

The COVID-19 pandemic and global environmental change: Emerging research needs

The outbreak of COVID-19 raised numerous questions on the interactions between the occurrence of new infections, the environment, climate and health. The European Union requested the H2020 HERA project which aims at setting priorities in research on environment, climate and health, to identify relevant research needs regarding Covid-19. The emergence and spread of SARS-CoV-2 appears to be related to urbanization, habitat destruction, live animal trade, intensive livestock farming and global travel. The contribution of climate and air pollution requires additional studies. Importantly, the severity of COVID-19 depends on the interactions between the viral infection, ageing and chronic diseases such as metabolic, respiratory and cardiovascular diseases and obesity which are themselves influenced by environmental stressors. The mechanisms of these interactions deserve additional scrutiny. Both the pandemic and the social response to the disease have elicited an array of behavioural and societal changes that may remain long after the pandemic and that may have long term health effects including on mental health. Recovery plans are currently being discussed or implemented and the environmental and health impacts of those plans are not clearly foreseen. Clearly, COVID-19 will have a long-lasting impact on the environmental health field and will open new research perspectives and policy needs.     

Spatial variation of biological and pedological properties in an area affected by a metallurgical mercury plant: Almadenejos (Spain)

Almadén, Spain, has the most important known cinnabar deposits, which have provided a third of the entire world production of Hg, and has been the scene for numerous studies on Hg. This mining district includes several mines where cinnabar has been extracted in the past two millennia as well as facilities related to the production of primary Hg. The aim of the work is to evaluate the spatial distribution of Hg in the soil-plant system within an area where intense activity occurred over a long period. An abandoned metallurgical plant from the 17th-18th centuries was chosen as the study area, situated in Almadenejos a distance of 12 km from Almadén. Nowadays, this plot is covered with cinnabar mine tailings and it is used by village inhabitants for livestock grazing. The area has elevated Hg concentrations of natural origin and from human activities. Soil parameters are similar within the study area; however, data reveal high variability in total and available Hg concentrations in soils, making it difficult to establish a trend. Marrubium vulgare L. has been studied due to its abundance in the plot, and there is no evidence of phenological toxicity. In spite of elevated Hg concentrations, high biological activity is found in the sampled soils. All these characteristics, spatial variation, high Hg concentration, good biological activity, make this a particularly good area for studies involving Hg.     

Early to Middle Devonian granitic and volcanic rocks from the central Gulf of Maine

Cashes Ledge igneous suite in the central Gulf of Maine is represented by 10 granitic and two felsic tuff samples collected from bedrock outcrops using the submersible Alvin in 1971–1972 and archived at the Woods Hole Oceanographic Institute. Laser ablation ICP-MS analyses of zircon grains yielded crystallization ages of 414.9 ± 1.1 Ma and 399.7 ± 1.5 Ma for two alkali feldspar granite samples, 407.0 ± 1.9 Ma for a syenogranite sample, and 384.4 ± 2.3 Ma and 383.9 ± 1.6 Ma for two felsic tuff samples. The samples contain iron-rich mafic minerals, including aegirine-augite, grunerite/ferroedenite, and annite. Most of the samples are alkaline to slightly peralkaline, with high concentrations of SiO₂, Y, Zr, Nb, and REE, strong negative Eu anomalies, and positive epsilon Nd values (1.8 to 3.7). The suite resembles part of a belt of similar Silurian–Devonian rocks with ages between 426 and 370 Ma now recognized in the central part of Avalonia in southeastern New England. They formed in a long-lived, likely extensional regime linked to subduction and subsequent complex transcurrent motions among Ganderia, Avalonia, and Meguma, culminating in the closure of the Rheic Ocean.     

Groundwater salinization in the Azores archipelago (Portugal)

Groundwater salinization in coastal regions causes severe constraints to water supply and economic losses to society worldwide. In the Azores archipelago, groundwater abstraction in wells drilled in coastal aquifers is very important for water supply, and quality problems have been reported. Therefore, a groundwater chemistry dataset from wells was compiled to study groundwater salinization in these aquifers. Waters are mainly of the Na–Cl type, presenting a slightly acidic to slightly alkaline character, with a pH between 5.63 and 8.50 (median 7.40). Electrical conductivity measurements range from 127 to 9,670 μS/cm (median 862), suggesting highly variable mineralization, with higher values observed on Santa Maria, São Miguel, Pico, Graciosa, and São Jorge islands. The major-ion composition reflects the contribution of seawater to the groundwater compositional evolution, which is essentially explained by seawater intrusion into wells. In many samples, exchange reactions of Na⁺ + K⁺ for Ca²⁺ + Mg²⁺ are associated with salinization. The seawater fraction in groundwater composition reaches a maximum of 22.5%. These results are extremely challenging to water managers in the Azores because failure to comply with national water quality regulations and with European Union groundwater directive requirements often occurs.