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The use of acoustic detectors to investigate differential use of habitat by bats has become increasingly common. However, in many of these studies, authors failed to clearly articulate assumptions a priori. For example, spatial and temporal scales were rarely defined. True replication is rarely reported, suggesting that authors assume that these systems are both spatially and temporally static. In this study, we attempted to clearly identify underlying assumptions of this technique, thereby limiting level of inference to a clearly defined and repeatable degree. We followed strict assumptions beforehand and were able to classify bat calls into guilds based on acoustic data. Lack of experience in acoustic identification by technicians did not affect the outcome, as guilds were based on bat call sequences following strict rules of classification. Individuals in guilds were not randomly distributed across sample locations. However, distribution of guild members did not suggest differential use of habitat, as within habitat variation was often greater than that observed among types of habitat. Explicitly stating assumptions before surveys were conducted ‘protected’ us from making incorrect inferences. We suggest that care be taken when attempting to infer differential use of habitat by bats using acoustic techniques.
We measured the shape of pinnae from fluid-preserved, museum specimens of 33 Myotis californicus and 39 M. ciliolabrum and cranial characters from 40 skulls of each species. We also measured 40 specimens of Eptesicus fuscus, which were used as an outgroup. Significant differences were found in aural shape and tragus height between the two species of Myotis. Archived echolocation calls from the two species from across the range segregated, further suggesting that morphological and call characters are intercorrelated. We tested this relationship using 17 M. californicus and 12 M. ciliolabrum captured in the field for external measurements and echolocation call recordings (n = 1,124 calls in 52 call files, x = 2.3 call files per released bat), and found significant differences (most P < 0.001) in pinnae and call morphology between M. ciliolabrum and M. californicus similar to those observed in ‘museum’ samples. We found that small interspecific differences in pinna shape and size are correlated with differences in the frequency ranges (larger pinna, lower frequency).
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