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Because of widespread habitat fragmentation, maintenance of landscape connectivity has become a major focus of conservation planning, but empirical tests of animal movement in fragmented landscapes remain scarce. We conducted a translocation experiment to test the relative permeability of three landscape elements (open habitat, shrubby secondary vegetation, and wooded corridors) to movement by the Chucao Tapaculo (Scelorchilus rubecula), a forest understory bird endemic to South American temperate rainforest. Forty-one radio-tagged subjects were translocated (individually) to three landscape treatments consisting of small release patches that were either entirely surrounded by open habitat (pasture), entirely surrounded by dense shrubs, or linked to other patches by wooded corridors that were otherwise surrounded by open matrix. The number of days subjects remained in release patches before dispersal (a measure of habitat resistance) was significantly longer for patches surrounded by open habitat than for patches adjoining corridors or surrounded by dense shrubs. These results indicate that open habitat significantly constrains Chucao dispersal, in accord with expectation, but dispersal occurs equally well through wooded corridors and shrub-dominated matrix. Thus, corridor protection or restoration and management of vegetation in the matrix (to encourage animal movement) may be equally feasible alternatives for maintaining connectivity.

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Mixed‐species animal groups (MSGs) are widely acknowledged to increase predator avoidance and foraging efficiency, among other benefits, and thereby increase participants' fitness. Diversity in MSG composition ranges from two to 70 species of very similar or completely different phenotypes. Yet consistency in organization is also observable in that one or a few species usually have disproportionate importance for MSG formation and/or maintenance. We propose a two‐dimensional framework for understanding this diversity and consistency, concentrating on the types of interactions possible between two individuals, usually of different species. One axis represents the similarity of benefit types traded between the individuals, while the second axis expresses asymmetry in the relative amount of benefits/costs accrued. Considering benefit types, one extreme represents the case of single‐species groups wherein all individuals obtain the same supplementary, group‐size‐related benefits, and the other extreme comprises associations of very different, but complementary species (e.g. one partner creates access to food while the other provides vigilance). The relevance of social information and the matching of activities (e.g. speed of movement) are highest for relationships on the supplementary side of this axis, but so is competition; relationships between species will occur at points along this gradient where the benefits outweigh the costs. Considering benefit amounts given or received, extreme asymmetry occurs when one species is exclusively a benefit provider and the other a benefit user. Within this parameter space, some MSG systems are constrained to one kind of interaction, such as shoals of fish of similar species or leader–follower interactions in fish and other taxa. Other MSGs, such as terrestrial bird flocks, can simultaneously include a variety of supplementary and complementary interactions. We review the benefits that species obtain across the diversity of MSG types, and argue that the degree and nature of asymmetry between benefit providers and users should be measured and not just assumed. We then discuss evolutionary shifts in MSG types, focusing on drivers towards similarity in group composition, and selection on benefit providers to enhance the benefits they can receive from other species. Finally, we conclude by considering how individual and collective behaviour in MSGs may influence both the structure and processes of communities.

For five species of endemic understory birds (  families Rhinocryptidae, Furnariidae) inhabiting fragmented temperate rainforest in southcentral Chile, we distinguished between vegetated corridors functioning as living space and those potentially suitable for short‐distance movements only. In the first phase of the study, we surveyed 24 forested corridors ≤50 m wide using passive and song‐playback censuses. Corridor width determined species presence or absence, whereas the number of individuals increased with width and understory vegetation density. Birds were infrequently encountered in corridors ≤10 m wide but were always present in corridors 25–50 m wide. Birds present in intermediate‐width (11–24 m) corridors were detected significantly less often during passive than playback census, suggesting that these birds exhibited conspicuous territorial display less frequently than those present in wider corridors, where passive and playback census yielded similar detection rates. Corridors approximately 10–25 m wide, therefore, may be transitional between corridors too narrow for most regular uses and those sufficiently wide for birds to establish territories. Also, bird abundance decreased as the ratio of corridor length to width ( L /  W) increased. Almost no birds were detected in corridors with L / W ≥ 10, suggesting the existence of a threshold value for the influence of L / W on corridor use. In the second phase of the study, taped‐song playback experiments in corridors ≤10 m wide showed that all five species traveled in them for short distances: 52% of respondents moved up to 50 m from forest patches into narrow corridors. Availability of dense understory vegetation was the primary predictor of birds' responses to playback and may determine their willingness to use minimal corridors for short movements. We suggest that corridors for endemic rainforest‐understory birds living in agricultural landscapes of southern Chile can be designed to fulfill distinct functions.

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