For birds, we tested the efficacy of a technique used to obtain faecal samples and their seed content from bats by placing plastic sheets below mist nets. This method was compared with that of collecting faecal samples using cotton bags. Plastic sheets were placed below each of eight mist nets to obtain faecal samples from birds caught in cloud forest remnants. Each bird was then placed separately in a cotton bag to catch any other seeds excreted. There were 84 faecal samples in total: 64 with no seeds and 20 with seeds; of the latter 65% were obtained from the plastic sheets. A total of 407 seeds were collected, 317 from 11 plant species were collected on the plastic sheets and 90 belonging to six plant species in the bags. Seed richness and abundance were significantly greater for samples obtained using the plastic sheets than with the cotton bags. Although the number of bird faecal samples obtained did not differ between methods (13 vs 7), with the plastic sheets the number of faecal samples with seeds increased. Thus, to obtain more representative faecal samples from frugivorous birds, we strongly recommend the use of plastic sheets as part of the technique.

A range of species eating the same fruit suggests that niche overlap can occur, along with potential competition among them. To test if the overlap in the coterie of fruit-eating birds is larger than would be expected by chance, we performed a comparison with coteries generated from the use of null models. The study was carried out in an area of savanna woodland of 127 ha in Uberlândia city, Brazil. Four individuals of five zoochorous plant species were selected and 60 h of focal observation was performed on each species. We recorded species of birds that consumed fruits and the quantity of fruit removed. We used an index of Proportional Similarity (PS) between each pair of plant species, using the relative proportion of fruit taken by each bird species of each plant. The mean value of observed PS was compared with the mean PS generated from randomizations. Thirty-six bird species were recorded eating fruits in the selected plant species. The mean overlap observed (PS = 0.183) was significantly higher (P = 0.032) than the mean overlap generated by the null models (PS = 0.123). This pattern suggests that competition is not an important factor in the formation of the coteries and there is sharing of resources. The abundance of fruits offered, especially in the rainy season, and the relatively low number of frugivorous species may be factors explaining the low influence of interactions and therefore the overlap between coteries.

The fruits of Melastomataceae are consumed by many Neotropical frugivorous birds. Several studies have reported segregated fruiting seasons of melastomes, but this pattern is not widespread. The segregated fruiting phenologies of congeneric sympatric species may be an evolutionary response to reduce competition for seed dispersers. Alternatively, aggregated fruiting phenologies may be favoured if local fruit abundance attracts more frugivores, thus enhancing seed dispersal. We monitored melastome fruiting in transects over a 2-y period at a cloud-forest site in the Colombian Andes. Fruiting periods of nine melastome species were aggregated and fruiting peaks coincided with rainy seasons. In a separate 6-mo study, observations at focal plants revealed that 47 of 61 bird species fed on 10 species of melastome, representing 37.4% of feeding events observed. Melastomes were consumed by birds in a higher proportion than expected from their availability and peak melastome fruit abundance coincided with the breeding season of the frugivore community, when melastomes constituted 54% of feeding records. Melastomes interact with a large number of bird species throughout their annual cycles, and seem to constitute pivotal elements that sustain the frugivore community in montane forests.

Plants potentially compete for seed dispersal. Selection may favour temporally segregated fruiting phenologies to minimize this competition and also to maintain resident populations of dispersal agents. Alternatively, selection may favour temporally aggregated fruiting phenologies when the effectiveness of seed dispersal agents varies seasonally or when large, synchronous fruit displays enhance dispersal. These evolutionary scenarios assume that plants share seed dispersal agents. This assumption and temporal overlap in fruiting phenologies were evaluated for the Miconia and Psychotria of central Panama. These two genera accounted for 18 and 27%, respectively, of 1096 fleshy fruits found in regurgitation or faecal samples taken from 2054 birds of 103 species netted in the forest understorey. Two species of manakins accounted for 62% (123/200) of all Miconia fruit taken. Three species of manakins and three species of migratory thrushes accounted for 97% (282/292) of all Psychotria fruits taken. There is a high potential for intrageneric competition for seed dispersal for both plant genera. Null model analyses showed that the fruiting phenologies of Miconia (14 species) are segregated in time, while fruiting of Psychotria (21 species) is highly aggregated. The Miconia were found in up to 24% of the diet samples for the two manakin species, suggesting that Miconia may be a critical resource for both species. The Psychotria fruited when the diversity of understorey fruits was greatest, suggesting a high potential for both intra- and extrageneric competition. The abundance and nomadism of the six bird species that consumed most Psychotria fruit peaked when the Psychotria fruited, supporting the enhancement hypothesis.