2016
DOI: 10.3161/15081109acc2016.18.2.014
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Echolocation Calls and Flight Behaviour of the Elusive Pied Butterfly Bat (Glauconycteris superba), and New Data on Its Morphology and Ecology

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Cited by 9 publications
(16 citation statements)
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“…Localization was used for eight purposes in animal behavior and ecology, with 35 studies using localization for multiple purposes (Figure 3). Twenty‐six studies assessed individual animals' positions or movement, such as responses to conspecific or interspecific disturbances (e.g., Campbell & Francis, 2012; Collier, Blumstein, et al, 2010; Langemann, Peake, Tavares, & McGregor, 2000), flight speed or style in bats (e.g., Grodzinski, Spiegel, Korine, & Holderied, 2009; Ing et al, 2016; Miller & Treat, 1993), positions of displaying male birds and frogs (e.g., Grafe, 1997; Patricelli & Krakauer, 2010), and determining the position of individual predator bats when insects' auditory organs perceived these predators (Goerlitz, ter Hofstede, Zeale, Jones, & Holderied, 2010; Roeder, 1966; Schul, Matt, & Helversen, 2000). Twenty‐four studies quantified the amplitude or directionality of animal sounds, using localization to account for the animal's distance or position in relation to the microphone; this method was especially common in studies of bats (e.g., Holderied & Helversen, 2003; Jakobsen, Olsen, & Surlykke, 2015; Lewanzik & Goerlitz, 2018), but was also used to study elephants (Hedwig, DeBellis, & Wrege, 2018; Wrege, Rowland, Keen, & Shiu, 2017) and birds (Dantzker, Deane, & Bradbury, 1999; Patricelli, Dantzker, & Bradbury, 2007, 2008).…”
Section: Resultsmentioning
confidence: 99%
“…Localization was used for eight purposes in animal behavior and ecology, with 35 studies using localization for multiple purposes (Figure 3). Twenty‐six studies assessed individual animals' positions or movement, such as responses to conspecific or interspecific disturbances (e.g., Campbell & Francis, 2012; Collier, Blumstein, et al, 2010; Langemann, Peake, Tavares, & McGregor, 2000), flight speed or style in bats (e.g., Grodzinski, Spiegel, Korine, & Holderied, 2009; Ing et al, 2016; Miller & Treat, 1993), positions of displaying male birds and frogs (e.g., Grafe, 1997; Patricelli & Krakauer, 2010), and determining the position of individual predator bats when insects' auditory organs perceived these predators (Goerlitz, ter Hofstede, Zeale, Jones, & Holderied, 2010; Roeder, 1966; Schul, Matt, & Helversen, 2000). Twenty‐four studies quantified the amplitude or directionality of animal sounds, using localization to account for the animal's distance or position in relation to the microphone; this method was especially common in studies of bats (e.g., Holderied & Helversen, 2003; Jakobsen, Olsen, & Surlykke, 2015; Lewanzik & Goerlitz, 2018), but was also used to study elephants (Hedwig, DeBellis, & Wrege, 2018; Wrege, Rowland, Keen, & Shiu, 2017) and birds (Dantzker, Deane, & Bradbury, 1999; Patricelli, Dantzker, & Bradbury, 2007, 2008).…”
Section: Resultsmentioning
confidence: 99%
“…As if to confirm the previous statement, after the manuscript for this paper was submitted, Ing et al (2016) and Hassanin et al (2017) reported on ten additional specimens from Mbiye island and the Yoko Forest Reserve (00°17′ N, 25°17′ E). Hassanin et al (2017) also described a new species of Glauconycteris, which is not covered in the current paper.…”
mentioning
confidence: 77%
“…At the end of the Miocene, around 6 ± 2 Mya, Glauconycteris diversified in Africa into three main groups, which today occupy different habitats: The lineage corresponding to G. variegata (which may also contain G. machadoi ) is predominantly associated with savannah, woodland, and bushveld habitats (Monadjem, Taylor, Cotterill, & Schoeman, ; Rambaldini, ); in the tropical rainforests, G. superba seems to be an open space forager, that is, concentrating its activity above the canopy (Ing et al., ), whereas all other species of Glauconycteris , which have a smaller size and a less conspicuous color pattern, are expected to be edge foragers, that is, exploiting the spaces immediately below the canopy, as do the majority of bat species living in Neotropical rainforests (Tiago Marques, Ramos Pereira, & Palmeirim, ). The basal diversification of Glauconycteris occurred when a brief event of aridity, between 6.5 and 6 Mya, was followed by more humid conditions (Bonnefille, ).…”
Section: Discussionmentioning
confidence: 99%
“…In G. egeria , we observed that the shoulder spot and dorsal flank stripe are confluent. In G. superba , there are two or rarely three white spots on each shoulder (Ing et al., ). In addition, two species are without body patterns or reticulated wings: G. atra sp.…”
Section: Discussionmentioning
confidence: 99%
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