Vision in echolocating bats - Fladdermus.net
Vision in echolocating bats - Fladdermus.net
Vision in echolocating bats - Fladdermus.net
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Predator surveillance and social behaviour<br />
As discussed earlier, vision seems to be important <strong>in</strong> escape behaviour<br />
(Chase 1981; Chase 1983; Mistry 1990). Presumably it is also important<br />
<strong>in</strong> detection of predators; it is much easier to approach a bl<strong>in</strong>dfolded bat<br />
than a non-bl<strong>in</strong>dfolded <strong>in</strong>dividual (Chase 1972). Species of the family<br />
Emballonuridae often fly earlier <strong>in</strong> the even<strong>in</strong>g than most other <strong>bats</strong>, and<br />
sometimes even <strong>in</strong> the afternoon and they often roost on exposed and<br />
well lit sites such as tree trunks (e.g. Bradbury & Vehrencamp 1976). A<br />
Saccopteryx sp. will quite easily detect an approach<strong>in</strong>g person, and take<br />
flight without emitt<strong>in</strong>g any echolocation calls (Suthers 1970), and<br />
Rhynconycteris naso seems to be disturbed more easily by see<strong>in</strong>g an<br />
approach<strong>in</strong>g figure at a distance, than by sudden sounds or vibrations at<br />
close range (Dalquest 1957). Vaughan and Vaughan (1986) noted that<br />
Lavia frons (Megadermatidae), which also roosts exposed, seems to be<br />
constantly alert dur<strong>in</strong>g the day, scann<strong>in</strong>g its surround<strong>in</strong>gs for predators. In<br />
fact, the authors almost never saw a bat with its eyes closed, and were<br />
never able to approach one undetected.<br />
The evidence for the use of vision <strong>in</strong> social behaviour is<br />
ma<strong>in</strong>ly anecdotal. Social groom<strong>in</strong>g occurs <strong>in</strong> the vampire Desmodus<br />
rotundus (Phyllostomidae) and may serve to identify <strong>in</strong>dividuals<br />
(Wilk<strong>in</strong>son 1986), although it is generally rare (Flem<strong>in</strong>g 1988). Goodw<strong>in</strong><br />
and Greenhall (1961) noted that avian vampire <strong>bats</strong> (Diaemus youngi)<br />
show groom<strong>in</strong>g behaviour when see<strong>in</strong>g a mirror reflection, <strong>in</strong>dicat<strong>in</strong>g that<br />
vision might be <strong>in</strong>volved <strong>in</strong> this behaviour. Sometimes <strong>bats</strong> are also<br />
observed to imitate other <strong>in</strong>dividuals groom<strong>in</strong>g themselves (Vaughan &<br />
Vaughan 1986).<br />
Some bat species have dist<strong>in</strong>ct fur patterns, which may<br />
serve as visual recognition signals (Fenton 2001), <strong>in</strong> addition to scents<br />
and sound, although fur patterns may also serve as camouflage<br />
(Neuweiler 2000). Threat displays are common <strong>in</strong> for example Carollia<br />
perspicillata (Phyllostomidae), and <strong>in</strong>cludes w<strong>in</strong>g shak<strong>in</strong>g, harsh sounds,<br />
and aggressive looks such as extension of the tongue (Flem<strong>in</strong>g 1988).<br />
Sexual displays are also common. The monogamous Lavia frons and<br />
Cardioderma cor (Megadermatidae), perform stereotypical circular<br />
flights, described as aerial ballets (McWilliam 1987; Vaughan &<br />
Vaughan 1986). Among Saccopteryx bil<strong>in</strong>eata (Emballonuridae), the<br />
males defend territories where they ma<strong>in</strong>ta<strong>in</strong> harems. In front of the<br />
females of the harem, they perform sexual displays, which <strong>in</strong>clude<br />
stereotyped s<strong>in</strong>g<strong>in</strong>g, and also shak<strong>in</strong>g of w<strong>in</strong>gs and hover<strong>in</strong>g. The w<strong>in</strong>g<br />
shak<strong>in</strong>g presumably enhances the effect of olfactory glands by spread<strong>in</strong>g<br />
pheromones, but it may also function as a visual signal to draw the<br />
females’ attention (Chase 1972).<br />
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