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 3<br />
dom<strong>in</strong>ant plant families seemed to be represented <strong>in</strong> the diets as represented <strong>in</strong> the<br />
overall sample. The same is true for growth form (Table 3). Most consumers favour<br />
berries and drupes, but for rodents there was a trend for select<strong>in</strong>g drupes. Even though<br />
soft and juicy fruit made up most of the sample, nocturnal lemurs and fly<strong>in</strong>g foxes<br />
selected this pulp type significantly more often than other pulp types. The latter also<br />
favoured arillate fruits (Table 3). For colour a selection was noticed towards red and<br />
purple fruits by all <strong>frugivore</strong> bird species, whereas mammals ate whatever colour was<br />
available. Most fruits <strong>in</strong> the <strong>littoral</strong> <strong>forest</strong> had an odour and were probably selected <strong>in</strong> this<br />
way, except for Coracopsis nigra, which fed ma<strong>in</strong>ly on odourless fruits (Table 3). For the<br />
nocturnal lemur species fruits with a th<strong>in</strong> husk were favoured. The other consumers did<br />
not seem to avoid the few dehiscent and thick-husked fruits present (Table 3). In all<br />
animal species no difference <strong>in</strong> seed protection could be found between diet and the<br />
overall dataset (Table 3). The few preferences <strong>in</strong>dicated above appeared to be nonsignificant<br />
after correction by sequential Bonferroni.<br />
Fly<strong>in</strong>g foxes were the only consumer species, which preferred multi-seeded fruits,<br />
while the diet of the other animals did not differ from what was available (Table 4). Initially<br />
many significant preferences could be found related to fruit and seed size and weight.<br />
However after sequential Bonferroni adjustment, only the frugivorous birds seem to select<br />
significantly smaller and lighter fruits. Coracopsis nigra also prefers lighter fruits and<br />
Pteropus rufus smaller seeds. Contrarily the rodents clearly favour heavier fruits and<br />
larger seeds. (Table 4).<br />
Biochemical Characteristics<br />
Water was the dom<strong>in</strong>ant constituent of fresh pulp (median 76.0%). On a dry mass basis,<br />
both acid (22.6%) and neutral (32.0%) detergent fibre contents were high. The median<br />
sugar content was 19.2%. Median lipid content of fruits was 3.1%, total nitrogen 0.9%,<br />
and extractable prote<strong>in</strong> 2.8%. Tann<strong>in</strong> values were very low <strong>in</strong> our dataset with a median<br />
value of 0.2%. Enzymatic analyses of all fruits yielded median values of 3.6%<br />
saccharose, 1.8% glucose, and 1.8% fructose.<br />
As for fats, frugivorous birds seemed to select fruits with a high lipid content, while<br />
the opposite was true for E. f. collaris and P. rufus (Table 4). Neither total nitrogen nor<br />
extractable prote<strong>in</strong> seemed to <strong>in</strong>fluence fruit choice for any of the consumer species, nor<br />
did water content or acid detergent fibre. Cheirogaleus spp. and Microcebus rufus<br />
selected fruits with high sugar content but this trend was not significant (Cheirogaleus<br />
spp. P=0.06, M. rufus P=0.19). However when look<strong>in</strong>g at saccharose, glucose, and<br />
fructose concentrations separately, preferences were significant for Cheirogaleus spp.<br />
(Table 4). The same trend existed for M. rufus (saccharose P=0.17, glucose P=0.11,<br />
fructose P=0.056). Tann<strong>in</strong>s were consumed as present <strong>in</strong> the overall database but<br />
Coracopsis nigra <strong>in</strong>cluded fruits with significantly higher tann<strong>in</strong> content. In the diet of M.<br />
rufus neutral detergent fibre was significantly lower than <strong>in</strong> fruits, which were not<br />
consumed (Table 4). None of these preferences rema<strong>in</strong>ed significant after sequential<br />
Bonferroni adjustment.<br />
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