2W1 Summary 1.Omnivory enables animals to fill more than one trophic niche, providing access to a wider variety of food resources with potentially higher nutrient value, particularly when resources become scarce. Animals can achieve omnivory using different strategies, for example opportunistic foraging, or switching between multiple trophic niches. 2. The Neotropical bat Glossophaga soricina (Pallas, 1766) is a common and widespread species known for nectar feeding, but it also eats fruit and insects. Approaching stationary objects (flowers and fruits) or moving objects (insects) poses different sensory tasks and should require different echolocation behaviours. Here we tested the contrasting hypothesis that G. soricina can approach both stationary and moving objects using the same echolocation behaviour, thus feeding at different trophic levels by a single sensory mechanism. 3. Using DNA barcoding, we demonstrate that G. soricina eats beetles (Coleoptera), flies (Diptera) and noctuid moths with bat-detecting ears. Laboratory observations show that G. soricina actively hunts for prey so insect consumption does not appear to be opportunistic. After capture, individuals consumed prey while perched and manipulated them with jaw, thumb, wrist and wing movements, but food handling was longer and chewing rate slower than in obligate insectivores. 4. In contrast to most insectivorous bats, the echolocation calls of G. soricina are of high frequency and low intensity, and G. soricina did not produce feeding buzzes when approaching insects. An acoustic model of detection distances shows that its low-intensity calls fail to trigger the auditory neurons of eared moths, allowing G. soricina to overcome auditory prey defences. 5. Individuals achieved niche flexibility using a unique but generalist behavioural approach rather than employing two different specialist methods. Our findings provide a novel insight into the functional mechanisms of insect capture in G. soricina and highlight the importance of considering niche flexibility in classifying trophic links in ecological communities.
The expansion of the wind energy industry has had benefits in terms of increased renewable energy production but has also led to increased mortality of migratory bats due to interactions with wind turbines. A key question that could guide bat-related management activities is identifying the geographic origin of bats killed at wind-energy facilities. Generating this information requires developing new methods for identifying the geographic sources of individual bats. Here we explore the viability of assigning geographic origin using trace element analyses of fur to infer the summer molting location of eastern red bats (Lasiurus borealis). Our approach is based on the idea that the concentration of trace elements in bat fur is related through the food chain to the amount of trace elements present in the soil, which varies across large geographic scales. Specifically, we used inductively coupled plasma–mass spectrometry to determine the concentration of fourteen trace elements in fur of 126 known-origin eastern red bats to generate a basemap for assignment throughout the range of this species in eastern North America. We then compared this map to publicly available soil trace element concentrations for the U.S. and Canada, used a probabilistic framework to generate likelihood-of-origin maps for each bat, and assessed how well trace element profiles predicted the origins of these individuals. Overall, our results suggest that trace elements allow successful assignment of individual bats 80% of the time while reducing probable locations in half. Our study supports the use of trace elements to identify the geographic origin of eastern red and perhaps other migratory bats, particularly when combined with data from other biomarkers such as genetic and stable isotope data.
As molecular tools for assessing trophic interactions become common, research is increasingly focused on the construction of interaction networks. Here, we demonstrate three key methods for incorporating DNA data into network ecology and discuss analytical considerations using a model consisting of plants, insects, bats and their parasites from the Costa Rica dry forest. The simplest method involves the use of Sanger sequencing to acquire long sequences to validate or refine field identifications, for example of bats and their parasites, where one specimen yields one sequence and one identification. This method can be fully quantified and resolved and these data resemble traditional ecological networks. For more complex taxonomic identifications, we target multiple DNA loci, for example from a seed or fruit pulp sample in faeces. These networks are also well resolved but gene targets vary in resolution and quantification is difficult. Finally, for mixed templates such as faecal contents of insectivorous bats, we use DNA metabarcoding targeting two sequence lengths (157 and 407 bp) of one gene region and a MOTU, BLAST and BIN association approach to resolve nodes. This network type is complex to generate and analyse, and we discuss the implications of this type of resolution on network analysis. Using these data, we construct the first molecular‐based network of networks containing 3,304 interactions between 762 nodes of eight trophic functions and involving parasitic, mutualistic and predatory interactions. We provide a comparison of the relative strengths and weaknesses of these data types in network ecology.
Carcasses provide an important resource for assessing the vulnerability of bat species and sexes to threats, but the reliability of sex data derived from the external morphology (sexmorph) of bat carcasses remains uncertain. We used genetic‐based assessment of sex (sexgen) to evaluate the effect of carcass age and searcher identity on sexmorph‐based assessments of eastern red (Lasiurus borealis) and hoary (Lasiurus cinereus) bat carcasses identified by 15 different searchers at a wind‐energy facility. The proportion of carcasses for which sexmorph was unknown increased from 0.11 for those recovered within a day of death, to 0.56 within 2–3 days of death, and to ≥0.82 at ≥4 days after death. The proportion of carcasses for which sexmorph was correct decreased from 0.9 for those recovered within a day of death, to 0.65 within 2–3 days of death, and to 0.25 at ≥4 days after death. The proportion of sexmorph misidentifications of the 108 fresh carcasses (collected within 24 hours of death) varied (0.0–0.43) among searchers. These results suggest that sexmorph‐based assessments should be limited to fresh carcasses. Furthermore, additional training of people who collect and identify bat carcasses from renewable‐energy facilities may improve the accuracy of sexmorph data obtained from carcasses. © 2018 The Wildlife Society.
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