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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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