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Species richness [frugivore species 30 min −1 tree −1 ] (A), abundance [frugivore individuals 30 min −1 tree −1 ] (B) and fruits  

Species richness [frugivore species 30 min −1 tree −1 ] (A), abundance [frugivore individuals 30 min −1 tree −1 ] (B) and fruits  

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So far, it is poorly understood how differential responses of avian seed dispersers and fruit predators to changes in habitat structure and fruit abundance along land-use gradients may translate into consequences for the seed dispersal of associated plants. We selected a gradient of habitat modification (forest, semi-natural, and rural habitat) cha...

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Context 1
... accounted for 67% and fruit predators accounted for 33% of visits to S. aucuparia trees (16% seed predators and 17% pulp predators). Species richness (F 2,15 = 8.42, p = 0.0035), abundance (F 2,15 = 7.46, p = 0.0056) and fruit removal rate (F 2,15 = 4.08, p = 0.039) of seed dispersers decreased from forest to semi-natural to rural habitats (Fig. 2). At the same time, species richness (F 2,15 = 0.30, p = 0.75), abundance (F 2,15 < 0.1, p = 0.93) and fruit removal rate (F 2,15 < 0.1, p = 0.92) of fruit predators did not vary among habitats. Consequently, the proportion of fruits removed by seed dispersers tended to decrease from 90% (+5.7/−7.6) (back- transformed mean ± SE) in ...
Context 2
... effects of fruit abundance and tree cover, we introduced these covariates into the preceding models. Species richness and abundance of seed dispersers increased with an increase in tree cover, while fruit removal rate and the proportion of fruits removed by seed dispersers increased with an increase in fruit abundance (see Appendix A: Table S1; Fig. S2). After inclusion of tree cover and fruit abundance, habitat was not significant anymore in explaining variation in any of the models (see Appendix A: Table S1). Com- parisons of all multiple models based upon AIC c revealed that tree cover best explained variation in species richness (r 2 = 0.52, F 1,16 = 17.5, p < 0.001) and ...
Context 3
... abun- dance of seed dispersers indirectly via its effect on tree cover, while fruit removal and the proportion of fruits removed by seed dispersers were influenced via the effect on fruit abun- dance. Species richness, abundance and fruit removal rate of fruit predators did not vary with fruit abundance or tree cover (see Appendix A: Table S1; Fig. ...

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... In this later case, the cost of transporting acorns from the shrubland to the forest (e.g., higher time, energy expenditure and predation risk during transport) probably does not compensate for the lower jay predation risk provided by the forest to hide acorns. As shown for other forest frugivorous species (García and Ortiz-Pulido, 2004;Albrecht et al., 2012), acorn dispersal in the shrubland by jays may be driven by acorn production because isolated trees usually have higher seed production than forest trees (Pausas et al., 2009;Morán-López et al., 2015). It is possible that habitat selection by jays and the spatial dispersal pattern observed in this study can also be influenced by acorn caching territories, mainly in the forest around theirs nests, as demonstrated in another corvid, the magpie (Martínez- Baroja et al., 2021). ...
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