Large-seeded plants are especially vulnerable to the loss of seed dispersers in small forest fragments. The palm Attalea humilis goes against this trend by reaching high abundances in small remnants. Productivity, seed dispersal and seed predation of A. humilis were investigated in two large (2400 and 3500 ha) and three small (19, 26 and 57 ha) Atlantic Forest fragments in southeastern Brazil. Palms in the small fragments produced more female inflorescences, resulting in a higher fruit production in these places. Seed dispersal rates were higher in the large fragments, where scatter hoarding was more frequent. Scolytine beetles were the main seed predators and damaged a larger number of seeds in small fragments, but predation by rodents and bruchine beetles was low irrespective of fragment size. As scolytines do not necessarily kill the seeds, low predation by bruchines and rodents, together with its own high productivity, allow A. humilis to be more abundant in small fragments despite the scarcity of its main dispersers. This increased abundance, by its turn, can increase competitive interactions between A. humilis and other plants in small fragments. Thus, abundance patterns of A. humilis are a good example of fragmentation affecting the balance of ecological interactions in a complex way, emphasizing the role of preserving ecological processes for conserving biodiversity in fragmented tropical landscapes.Abstract in Portuguese is available in the online version of this article.
Palms are important components of tropical forest plant communities, due both to their abundance (Henderson et al. 2000) and to the network of interactions with their pollinators and dispersers (Henderson 2002, Zona & Henderson 1989). Forest fragmentation alters the biotic and abiotic conditions of habitats (Ewers & Didham 2006, Fahrig 2003) and it has been observed that Attalea palms increase their densities in disturbed sites (Aguiar & Tabarelli 2009, Andreazzi et al. 2012, Lorenzi et al. 2004). Increased light availability (Salm 2005, Souza & Martins 2004), changes in seed dispersal and predation patterns (Andreazzi et al. 2012, Pimentel & Tabarelli 2004, Wright et al. 2000), and ability to recover after disturbance (Souza & Martins 2004) are among the main mechanisms that have been proposed to explain enhanced palm densities. However, how altered conditions following disturbances influence the dynamics of flower and fruit production is still little understood.
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