Fruit-frugivore interactions in a Malagasy littoral forest - Universiteit ...
Fruit-frugivore interactions in a Malagasy littoral forest - Universiteit ...
Fruit-frugivore interactions in a Malagasy littoral forest - Universiteit ...
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Chapter 3a<br />
Food selection<br />
Growth form<br />
A closer look at fruit characteristics for both eaten and available species seems to po<strong>in</strong>t at<br />
certa<strong>in</strong> food preferences, although at the same time other, non-significant, results were<br />
rather unexpected. For example accord<strong>in</strong>g to the analyses the fly<strong>in</strong>g foxes did not prefer<br />
to eat <strong>in</strong> large trees, which was unexpected as bats were most often observed and<br />
supposed to feed <strong>in</strong> large trees (Flem<strong>in</strong>g et al. 1987). The often larger fruit crop available<br />
at the same time <strong>in</strong> large trees, the more accessible position and the more easily<br />
detectable resources both for bats and researchers are probably responsible for this<br />
result. All important food resources <strong>in</strong> our diet list <strong>in</strong>volve large trees, but shrubs and<br />
smaller trees still account for almost 40%. The latter occur <strong>in</strong> larger numbers <strong>in</strong><br />
secondary <strong>forest</strong> and are more easily detected and eaten there. Old World pteropodids<br />
are known to be primarily canopy feeders (Flem<strong>in</strong>g et al. 1987) and prefer primary <strong>forest</strong><br />
to secondary <strong>forest</strong> (Banack 1998). In our data set most of the fruit species eaten grow <strong>in</strong><br />
<strong>in</strong>tact and primary <strong>forest</strong>. Both pioneer plant species as well as species from a later<br />
successive phase were exploited.<br />
<strong>Fruit</strong> type versus pulp type and water content<br />
The fly<strong>in</strong>g foxes eat ma<strong>in</strong>ly juicy berries with a high water content. Observations, ejecta<br />
pellets, and literature (Marshall 1983) confirm that fruit juices dom<strong>in</strong>ate the diet of fly<strong>in</strong>g<br />
foxes. As <strong>in</strong>dicated <strong>in</strong> Table 4, only for the parameter ‘pulp type’ a difference was found<br />
between eaten and available fruits, not for fruit type and water content but these<br />
parameters are often <strong>in</strong>ter-correlated. In most tropical <strong>forest</strong>s 50–90% of the plant<br />
species depend on animals for their dispersal (Howe and Smallwood 1982; Flem<strong>in</strong>g et al.<br />
1987) and among typical endozoochorous fruits juicy berries with a high water content<br />
form a large proportion, which stands also for the majority of available fruits <strong>in</strong> the humid<br />
<strong>littoral</strong> <strong>forest</strong> of Sa<strong>in</strong>te Luce.<br />
Odour and colour<br />
Most fruits eaten have an odour and even a strong one, which can be related to the bats’<br />
well-developed olfactory senses especially used for locat<strong>in</strong>g food (Marshall 1983; Kalko<br />
et al. 1996). Odour was a feature of most (65%) of the fruits available <strong>in</strong> the <strong>forest</strong>, which<br />
may expla<strong>in</strong> why analyses revealed that there was no significant preference for this trait.<br />
This abundance of odoriferous fruits is probably because a large amount of the available<br />
fruit species are dependant on mammals for seed dispersal and scent <strong>in</strong> general is also<br />
of major importance for mammals when locat<strong>in</strong>g and select<strong>in</strong>g ripe fruits. Besides good<br />
smell, the fly<strong>in</strong>g foxes have also developed large eyes and thus good vision which might<br />
further help them to locate fruits at night (Marshall 1983). Obviously colour is of little<br />
relevance s<strong>in</strong>ce they feed and forage at night and all nocturnal mammals are colour-bl<strong>in</strong>d<br />
(Corlett 1998). This is confirmed by the fact that selection of fruits <strong>in</strong> favour of a particular<br />
colour was not observed.<br />
Size versus mass<br />
Based on the number of seeds per dropp<strong>in</strong>g we presumed that t<strong>in</strong>y seeds of multi-seeded<br />
fruits with a length up to 1–3.5mm are likely to be automatically swallowed together with<br />
the fruit pulp. As for larger one- to two-seeded fruits, with seed length between 3.5–<br />
20mm, fruit sk<strong>in</strong> and seeds are most often spat out. This feed<strong>in</strong>g behaviour of dropp<strong>in</strong>g<br />
larger seeds and swallow<strong>in</strong>g t<strong>in</strong>y seeds together with fruit juices was also mentioned by<br />
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