Context Many Australian mammal species are highly susceptible to predation by introduced domestic cats (Felis catus) and European red foxes (Vulpes vulpes). These predators have caused many extinctions and have driven large distributional and population declines for many more species. The serendipitous occurrence of, and deliberate translocations of mammals to, ‘havens’ (cat- and fox-free offshore islands, and mainland fenced exclosures capable of excluding cats and foxes) has helped avoid further extinction. Aims The aim of this study was to conduct a stocktake of current island and fenced havens in Australia and assess the extent of their protection for threatened mammal taxa that are most susceptible to cat and fox predation. Methods Information was collated from diverse sources to document (1) the locations of havens and (2) the occurrence of populations of predator-susceptible threatened mammals (naturally occurring or translocated) in those havens. The list of predator-susceptible taxa (67 taxa, 52 species) was based on consensus opinion from >25 mammal experts. Key results Seventeen fenced and 101 island havens contain 188 populations of 38 predator-susceptible threatened mammal taxa (32 species). Island havens cover a larger cumulative area than fenced havens (2152km2 versus 346km2), and reach larger sizes (largest island 325km2, with another island of 628km2 becoming available from 2018; largest fence: 123km2). Islands and fenced havens contain similar numbers of taxa (27 each), because fenced havens usually contain more taxa per haven. Populations within fences are mostly translocated (43 of 49; 88%). Islands contain translocated populations (30 of 139; 22%); but also protect in situ (109) threatened mammal populations. Conclusions Havens are used increasingly to safeguard threatened predator-susceptible mammals. However, 15 such taxa occur in only one or two havens, and 29 such taxa (43%) are not represented in any havens. The taxon at greatest risk of extinction from predation, and in greatest need of a haven, is the central rock-rat (Zyzomys pedunculatus). Implications Future investment in havens should focus on locations that favour taxa with no (or low) existing haven representation. Although havens can be critical for avoiding extinctions in the short term, they cover a minute proportion of species’ former ranges. Improved options for controlling the impacts of cats and foxes at landscape scales must be developed and implemented.

Context Over the last 230 years, the Australian terrestrial mammal fauna has suffered a very high rate of decline and extinction relative to other continents. Predation by the introduced red fox (Vulpes vulpes) and feral cat (Felis catus) is implicated in many of these extinctions, and in the ongoing decline of many extant species. Aims To assess the degree to which Australian terrestrial non-volant mammal species are susceptible at the population level to predation by the red fox and feral cat, and to allocate each species to a category of predator susceptibility. Methods We collated the available evidence and complemented this with expert opinion to categorise each Australian terrestrial non-volant mammal species (extinct and extant) into one of four classes of population-level susceptibility to introduced predators (i.e. ‘extreme’, ‘high’, ‘low’ or ‘not susceptible’). We then compared predator susceptibility with conservation status, body size and extent of arboreality; and assessed changes in the occurrence of species in different predator-susceptibility categories between 1788 and 2017. Key results Of 246 Australian terrestrial non-volant mammal species (including extinct species), we conclude that 37 species are (or were) extremely predator-susceptible; 52 species are highly predator-susceptible; 112 species are of low susceptibility; and 42 species are not susceptible to predators. Confidence in assigning species to predator-susceptibility categories was strongest for extant threatened mammal species and for extremely predator-susceptible species. Extinct and threatened mammal species are more likely to be predator-susceptible than Least Concern species; arboreal species are less predator-susceptible than ground-dwelling species; and medium-sized species (35 g–3.5kg) are more predator-susceptible than smaller or larger species. Conclusions The effective control of foxes and cats over large areas is likely to assist the population-level recovery of ~63 species – the number of extant species with extreme or high predator susceptibility – which represents ~29% of the extant Australian terrestrial non-volant mammal fauna. Implications Categorisation of predator susceptibility is an important tool for conservation management, because the persistence of species with extreme susceptibility will require intensive management (e.g. predator-proof exclosures or predator-free islands), whereas species of lower predator susceptibility can be managed through effective landscape-level suppression of introduced predators.

Habitat loss and fragmentation are major threats to the survival of forest‐dependent fauna. We examined the abundance of small mammal species in forests, corridors, remnants of araucarian vine forest, and Araucaria cunninghamii plantations and pastures. None of the forest mammal species persisted following conversion of forest to pasture. Plantations supported lowered abundances of a subset of forest species that were mainly habitat generalists with respect to their occurrence in different floristic types of undisturbed native forest. Within plantations, an increased subcanopy cover was associated with a more forest‐like small mammal assemblage. Species' responses to habitat fragmentation varied. The floristic habitat generalists were largely tolerant of habitat fragmentation, their abundance being similar in forests, corridors, and remnants, and were capable of persisting in remnants a few hectares in area. Floristic habitat specialists were vulnerable to habitat fragmentation and thus were abundant in continuous forest, were less abundant in corridors, and were generally absent from remnants. Species that avoid the corridor matrix and are therefore constrained to the corridor may be disadvantaged by the linearity of the habitat, consistent with the predictions of central‐place foraging theory. Although small remnants and corridors provide habitat for some species, those that are more specialized in their use of undisturbed habitat types require the retention or reestablishment of large intact areas.

The structures of musical rhythm differ between cultures, despite the fact that the ability to entrain movement to musical rhythm occurs in virtually all individuals across cultures. To measure the influence of culture on rhythm processing, we tested East African and North American adults on perception, production, and beat tapping for rhythms derived from East African and Western music. To assess rhythm perception, participants identified whether pairs of rhythms were the same or different. To assess rhythm production, participants reproduced rhythms after hearing them. To assess beat tapping, participants tapped the beat along with repeated rhythms. We expected that performance in all three tasks would be influenced by the culture of the participant and the culture of the rhythm. Specifically, we predicted that a participant’s ability to discriminate, reproduce, and accurately tap the beat would be better for rhythms from their own culture than for rhythms from another culture. In the rhythm discrimination task, there were no differences in discriminating culturally familiar and unfamiliar rhythms. In the rhythm reproduction task, both groups reproduced East African rhythms more accurately than Western rhythms, but East African participants also showed an effect of cultural familiarity, leading to a significant interaction. In the beat tapping task, participants in both groups tapped the beat more accurately for culturally familiar than for unfamiliar rhythms. Moreover, there were differences between the two participant groups, and between the two types of rhythms, in the metrical level selected for beat tapping. The results demonstrate that culture does influence the processing of musical rhythm. In terms of the function of musical rhythm, our results are consistent with theories that musical rhythm enables synchronization. Musical rhythm may foster musical cultural identity by enabling within-group synchronization to music, perhaps supporting social cohesion.

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