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Arctic biodiversity is under threat from both climate-induced environmental change and anthropogenic activity. However, the rapid rate of change and the challenging conditions for studying Arctic environments mean that many research questions must be answered before we can strategically allocate resources for management. Addressing threats to biodiversity in the Arctic is further complicated by the region's complex geopolitics, as eight countries claim jurisdiction over the area, with multiple local considerations such as Indigenous sovereignty and resource rights. Here, we identify research priorities to serve as a starting point for addressing the most pressing threats to Arctic biodiversity. We began by collecting pressing research questions about Arctic biodiversity, thematizing them as either threats or actions, and then categorizing them further into 18 groups. Then, drawing on cross-disciplinary and global expertise of professionals in Arctic science, management, and policy, we considered the barriers to answering these questions and proposed potential solutions that could be implemented if barriers were overcome. Overall, our horizon scan provides an expert assessment of threats (e.g., species’ responses to climate change) and actions (e.g., a lack of fundamental information regarding Arctic biodiversity) needing attention and is intended to guide future conservation action within the Arctic. 

The transformations of complex metal oxides in aqueous settings must be studied to form a chemical understanding of how technologically relevant nanomaterials impact the environment upon disposal. Owing to the inherent heterogeneity and structural complexity of the ternary intercalation material Li(NixMnyCo1-x-y)O2 (NMC), the mechanisms of chemical processes at the solid–water interface are challenging to model. Here, density functional theory (DFT) + solvent ion methodology is used to study the energetics of stepwise release of two surface metals following unique pathways. The study spans different combinations of metal removal and also considers unique patterns of defects formed by modeling the NMC surface in supercells. The approach here also considers the equilibration of the surface with the surroundings between successive metal removals. A key finding is that a second metal removal prefers to proceed at a metal lattice site adjacent to the initial defect, and this is attributed in part to how the resulting slab with two metal vacancies maintains the most antiferromagnetic couplings between the remaining Ni/Mn. 

The conversion of forest to agriculture is considered one of the greatest threats to avian biodiversity, yet how species respond to habitat modification throughout the annual cycle remains unknown. We examined whether forest bird associations with agricultural habitats vary throughout the year, and if species traits influence these relationships. Using data from the eBird community‐science program, we investigated associations between agriculturally‐modified land cover and the occurrence of 238 forest bird species based on three sets of avian traits: migratory strategy, dietary guild, and foraging strategy. We found that the influence of agriculturally‐modified land cover on species distributions varied widely across periods and trait groups but highlighting several broad findings. First, migratory species showed strong seasonal differences in their response to agricultural land cover while resident species did not. Second, there was a migratory strategy by season interaction; Neotropical migrants were most negatively influenced by agricultural land cover during the breeding period while short‐distance migrants were most negatively influenced during the non‐breeding period. Third, regardless of season, some dietary (e.g. insectivores) and foraging guilds (e.g. bark foragers) consistently responded more negatively to agricultural land cover than others (e.g. omnivores and ground foragers, respectively). Fourth, there were greater differences among dietary guilds in their responses to agricultural land cover during the breeding period than during the non‐breeding period, perhaps reflecting how different habitat and ecological requirements enhance the susceptibility of some guilds during reproduction. These results suggest that management efforts across the annual cycle may be oversimplified and thus ineffective when based on broad ecological generalisations that are static in space and time. 

Abstract In two-dimensional chiral metal-halide perovskites, chiral organic spacers endow structural and optical chirality to the metal-halide sublattice, enabling exquisite control of light, charge, and electron spin. The chiroptical properties of metal-halide perovskites have been measured by transmissive circular dichroism spectroscopy, which necessitates thin-film samples. Here, by developing a reflection-based approach, we characterize the intrinsic, circular polarization-dependent complex refractive index for a prototypical two-dimensional chiral lead-bromide perovskite and report large circular dichroism for single crystals. Comparison with ab initio theory reveals the large circular dichroism arises from the inorganic sublattice rather than the chiral ligand and is an excitonic phenomenon driven by electron-hole exchange interactions, which breaks the degeneracy of transitions between Rashba-Dresselhaus-split bands, resulting in a Cotton effect. Our study suggests that previous data for spin-coated films largely underestimate the optical chirality and provides quantitative insights into the intrinsic optical properties of chiral perovskites for chiroptical and spintronic applications. 

Nanoscale complex metal oxides have transformed how technology is used around the world. A ubiquitous example is the class of electroreactive cathodes used in Li-ion batteries, found in portable electronics and electric cars. Lack of recycling infrastructure and financial drivers contribute to improper disposal, and ultimately, introduction of these materials into the environment. Outside of sealed operational conditions, it has been demonstrated that complex metal oxides can transform in the environment, and cause negative biological impact through leaching of cations into aqueous phases. Using a combined DFT and thermodynamics methodology, insights into the mechanism and driving forces of cation release can be studied at the molecular-level. Here, we describe design principles that can be drawn from previous collaborative research on complex metal oxide dissolution of the Li(Ni y Mn z Co 1−y−z )O 2 family of materials, and go on to posit ternary complex metal oxides in the delafossite structure type with controlled release behavior. Using equistoichiometric formulations in the delfossite structure, we use DFT and thermodynamics to model cation release. The release trends are discussed in terms of lattice stability, solution chemistry/solubility limits, and electronic/magnetic properties. Intercalation voltages are calculated and discussed as a predictive metric for potential functionality of the model materials.