The establishment of marine protected areas is often viewed as a conflict between conservation and fishing. We considered consumptive and nonconsumptive interests of multiple stakeholders (i.e., fishers, scuba divers, conservationists, managers, scientists) in the systematic design of a network of marine protected areas along California's central coast in the context of the Marine Life Protection ActPalabras Clave:áreas protegidas, biodiversidad marina, costos de conservación, esfuerzo de pesca, Marxan, planificación de la conservación, reservas marinas, zonas de exclusión de pesca
Ecoacoustics, the study of environmental sound, is a growing field with great potential for biodiversity monitoring. Audio recordings could provide a rapid, cost‐effective monitoring tool offering novel insights into ecosystem dynamics. More than 60 acoustic indices have been developed to date, which reflect distinct attributes of the soundscape, (i.e. the total acoustic energy at a given location, including noise produced by animals, machinery, wind and rain). However, reported patterns in acoustic indices have been contradictory, possibly because there is no accepted best practice for the collection and analysis of audio recordings. Here, we propose: (a) guidelines for designing studies using audio recordings for the rapid assessment of multiple sites; and (b) a workflow for comparing recordings with seven of the most commonly used indices, permitting discrimination among habitat‐specific soundscapes. We collected and analysed over 26,000 hr of recordings from 117 sites across a range of habitats in a human‐modified tropical landscape in central Panama; an order of magnitude more recordings than used in previously published studies. We demonstrate that: (a) Standard error variance of indices stabilizes within 120 hr of recordings from a single location. (b) Continuous recording should be used rather than subsample recording on a schedule; sub sampling is a common practice but delays capture of site variability and maximizing total duration of recording should be prioritized. (c) Use of multiple indices to describe soundscape patterns reveals distinct diel and seasonal soundscape patterns among habitats. We advocate collecting at least 120 hr of continuous recordings per site, and using a range of acoustic indices to categorize the soundscape, including the Acoustic Complexity Index, Acoustic Evenness Index, Acoustic Entropy Index and the Normalized Difference Soundscape Index. Differences among habitat types can be captured if multiple indices are used, and magnitude of variance is often more important than mean values. The workflow we provide will enable successful use of ecoacoustic techniques for environmental monitoring.
Secondary forest habitats are increasingly recognized for their potential to conserve biodiversity in the tropics. However, the development of faunal assemblages in secondary forest systems varies according to habitat quality and species‐specific traits. In this study, we predicted that the recovery of bird assemblages is dependent on secondary forest age and level of isolation, the forest stratum examined, and the species’ traits of feeding guild and body mass. This study was undertaken in secondary forests in central Panama; spanning a chronosequence of 60‐, 90‐, and 120‐year‐old forests, and in neighboring old‐growth forest. To give equal attention to all forest strata, we employed a novel method that paired simultaneous surveys in canopy and understory. This survey method provides a more nuanced picture than ground‐based studies, which are biased toward understory assemblages. Bird reassembly varied according to both habitat age and isolation, although it was challenging to separate these effects, as the older sites were also more isolated than the younger sites. In combination, habitat age and isolation impacted understory birds more than canopy‐dwelling birds. Proportions of dietary guilds did not vary with habitat age, but were significantly different between strata. Body mass distributions were similar across forest ages for small‐bodied birds, but older forest supported more large‐bodied birds, probably due to control of poaching at these sites. Canopy assemblages were characterized by higher species richness, and greater variation in both dietary breadth and body mass, relative to understory assemblages. The results highlight that secondary forests may offer critical refugia for many bird species, particularly specialist canopy‐dwellers. However, understory bird species may be less able to adapt to novel and isolated habitats and should be the focus of conservation efforts encouraging bird colonization of secondary forests.
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