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8 results for “hoary bat”
FIG. 1 in Analysis of Genomic Sequence Data Reveals the Origin and Evolutionary Separation of Hawaiian Hoary Bat Populations
FIG. 1.—Map of the Hawaiian Islands with collection sitesfor Hawaiian hoary bat tissues used inthis study. Sites with n> 1 are denoted with an asterisk.
FIG. 2 in Analysis of Genomic Sequence Data Reveals the Origin and Evolutionary Separation of Hawaiian Hoary Bat Populations
FIG. 2.—PCA result plot showing clustering of individual bats from four Hawaiian Islands using 21,808,031 SNPs. Sample information included in supplementary table S4, Supplementary Material online.
FIG. 4 in Analysis of Genomic Sequence Data Reveals the Origin and Evolutionary Separation of Hawaiian Hoary Bat Populations
FIG. 4.—SNAPP-based phylogenetic tree inference. (A) The maximum clade credibility or consensus tree, showing approximate divergence of hoary bats across the Hawaiian archipelago. The axis on the bottom of the figure corresponds to million years before present (Ma), using the emergence of Hawai'i (~0.43 Ma) as a calibration point (95% confidence intervals were given in square brackets). (B) The drawing of all sampled trees showing all ingroup nodes were supported by maximum posterior probabilities (1.00).
Data from: Inconspicuous echolocation in hoary bats (Lasiurus cinereus)
Echolocation allows bats to occupy diverse nocturnal niches. Bats almost always use echolocation, even when other sensory stimuli are available to guide navigation. Here, using arrays of calibrated infrared cameras and ultrasonic microphones, we demonstrate that hoary bats (Lasiurus cinereus) use previously unknown echolocation behaviors that challenge our current understanding of echolocation. We describe a novel call type ("micro" calls) that has three orders of magnitude less sound energy than other bat calls used in open habitats. We also document bats flying close to microphones (< 3 m) without producing detectable echolocation calls. Acoustic modeling indicates that bats are not producing calls that exceed 70-75 dB at 0.1 m, a level that would have little or no known use for a bat flying in the open at speeds exceeding 7 m s-1. This indicates that hoary bats sometimes fly without echolocation. We speculate that bats reduce echolocation output to avoid eavesdropping by conspecifics during the mating season. These findings might partly explain why tens of thousands of hoary bats are killed at wind turbines each year. They also challenge the long-standing assumption that bats—model organisms for sensory specialization—are reliant on sonar for nocturnal navigation.
Data from: Inconspicuous echolocation in hoary bats (Lasiurus cinereus)
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On following pages: 252. Northern Hoary Bat (Lasiurus cinereus); 253. Hawaiian Hoary Bat (Lasiurus semotus); 254. Eastern Red Bat (Lasiurus borealis); 255. Pfeiffer's Red Bat (Lasiurus pfeiffer); 256. Seminole Bat (Lasiurus seminolus); 257. Greater Red Bat (Lasiurus atratus); 258. Southern Red Bat (Lasiurus blossevilil); 259. Desert Red Bat (Lasiurus frantzi); 260. Cinnamon Red Bat (Lasiurus varius); 261. Minor Red Bat (Lasiurus minon; 262. Tacarcunan Bat (Lasiurus castaneus); 263. Hairy-tailed Bat (Lasiurus ebenus); 264. Jamaican Red Bat (Lasiurus degelidus); 265. Western Yellow Bat (Lasiurus xanthinus); 266. Northern Yellow Bat (Lasiurus intermedius); 267. Cuban Yellow Bat (Lasiurus insularis); 268. Southern Yellow Bat (Lasiurus egal). in Vespertilionidae
On following pages: 252. Northern Hoary Bat (Lasiurus cinereus); 253. Hawaiian Hoary Bat (Lasiurus semotus); 254. Eastern Red Bat (Lasiurus borealis); 255. Pfeiffer's Red Bat (Lasiurus pfeiffer); 256. Seminole Bat (Lasiurus seminolus); 257. Greater Red Bat (Lasiurus atratus); 258. Southern Red Bat (Lasiurus blossevilil); 259. Desert Red Bat (Lasiurus frantzi); 260. Cinnamon Red Bat (Lasiurus varius); 261. Minor Red Bat (Lasiurus minon; 262. Tacarcunan Bat (Lasiurus castaneus); 263. Hairy-tailed Bat (Lasiurus ebenus); 264. Jamaican Red Bat (Lasiurus degelidus); 265. Western Yellow Bat (Lasiurus xanthinus); 266. Northern Yellow Bat (Lasiurus intermedius); 267. Cuban Yellow Bat (Lasiurus insularis); 268. Southern Yellow Bat (Lasiurus egal).
On following pages 51 Pygmy Bamboo Bat (Tylonyctens pygmaea). 52 Indoma ayan Lesser Bamboo Bat (Tylonycreııs fu/vrda). 53 Sunda Lesser Bamboo Bat (Tylonycrers pachypus) 54 Tonkm Greater Bamboo Bat (Tylonycrerıs ronk nensrs) 55 Malayan Greater Bamboo Bat (Ty onyctens malayana) 56 Sumatran Greater Bamboo Bat (Tyloııycrerıs robusta/a) 57 Yok Don He meted Bat (Cass srre us yokdonens s) 58 Surat He meted Bat (Cassısrrel us dımıssus), 59 Rohu s Bat (Phıleror brachyptems). 60 Western False Prp strelle (Fels srrellus mackenzıeı), 61 Eastern False P pıstrelle (Fa s stre us rasmanıens s) 62 Ye ow-I pped Cave Bat (Vespade us douglasorum). 63 Northern Cave Bat (Vespade us caunnus). 64 Fmleysons Cave Bat (Vaspadelus fınlaysonı), 65 Eastern Cave Bat (Vespade us rroughtonı) 66 In and Forest Bat (Vespade us bavsrstodrı) 67 Eastern Forest Bat (Vespadelus pumılus), 68 Lıttle Forest Bat (Vespade/us vu/turnus) 69 Large Forest Bat (Vespadelus der! ngtonı), 70 Southern Forest Bat (Vespade us ragu us) 71 Large-eared P ed Bet (Cha noobus dwyerr) 72 L tt e Pıed Bat (Cha/ınolobus pıcarus). 73 Hoary Wettled Bet (Che/rnolobus rııgrogrısaus), 74 Gould's Wattled Bat (Chalınolobus gouldıı). 75 New Caledonıan Wattled Bat (Chalıno/obus neocaledonıcus) 76 Chocolate Wattled Bet (Chalnolobus morro), 77 New Zealand Long-taıled Bat (Chahnolobus ruberculetus) in Vespertilionidae
On following pages 51 Pygmy Bamboo Bat (Tylonyctens pygmaea). 52 Indoma ayan Lesser Bamboo Bat (Tylonycreııs fu/vrda). 53 Sunda Lesser Bamboo Bat (Tylonycrers pachypus) 54 Tonkm Greater Bamboo Bat (Tylonycrerıs ronk nensrs) 55 Malayan Greater Bamboo Bat (Ty onyctens malayana) 56 Sumatran Greater Bamboo Bat (Tyloııycrerıs robusta/a) 57 Yok Don He meted Bat (Cass srre us yokdonens s) 58 Surat He meted Bat (Cassısrrel us dımıssus), 59 Rohu s Bat (Phıleror brachyptems). 60 Western False Prp strelle (Fels srrellus mackenzıeı), 61 Eastern False P pıstrelle (Fa s stre us rasmanıens s) 62 Ye ow-I pped Cave Bat (Vespade us douglasorum). 63 Northern Cave Bat (Vespade us caunnus). 64 Fmleysons Cave Bat (Vaspadelus fınlaysonı), 65 Eastern Cave Bat (Vespade us rroughtonı) 66 In and Forest Bat (Vespade us bavsrstodrı) 67 Eastern Forest Bat (Vespadelus pumılus), 68 Lıttle Forest Bat (Vespade/us vu/turnus) 69 Large Forest Bat (Vespadelus der! ngtonı), 70 Southern Forest Bat (Vespade us ragu us) 71 Large-eared P ed Bet (Cha noobus dwyerr) 72 L tt e Pıed Bat (Cha/ınolobus pıcarus). 73 Hoary Wettled Bet (Che/rnolobus rııgrogrısaus), 74 Gould's Wattled Bat (Chalınolobus gouldıı). 75 New Caledonıan Wattled Bat (Chalıno/obus neocaledonıcus) 76 Chocolate Wattled Bet (Chalnolobus morro), 77 New Zealand Long-taıled Bat (Chahnolobus ruberculetus)
FIG. 3 in Analysis of Genomic Sequence Data Reveals the Origin and Evolutionary Separation of Hawaiian Hoary Bat Populations
FIG. 3.—Populationstructure inference based on STRUCTURE analysis of 199,921 sites for individual bats from four Hawaiian Islands. (A) Ad hoc statistic delta Kanalysis indicates a peak at the Κ = 5; (B) STRUCTURE population inference with Κ = 3, 4, 5. Sample information included in supplementary table S4, Supplementary Material online.
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