Abstract

While Psittaciformes (parrots and allies) are well recognized as highly-mobile seed predators, their role as seed dispersers has been overlooked until very recently. It remains to be determined whether this role is anecdotic or is a key mutualism for some plant species. We recently found that the large nut-like seeds of the two South American Araucaria tree species (A. araucana in Andean forests and A. angustifolia in Atlantic forests, weighing c. 3.5 and 7g, respectively) are frequently dispersed, and to long distances, by parrots. Moreover, both observational and experimental work demonstrated that dispersed seeds can germinate faster after partial predation by parrots. Here, we hypothesized that a third, even larger-seeded (17.5g) congeneric Australian species (A. bidwillii) is also dispersed by parrots. We surveyed 52 A. bidwillii and 42 A. cunninghamii (a sympatric species with small winged seeds, c. 0.2g) during the seeding period. We found that sulphur-crested cockatoos (Cacatua galerita) consumed large amounts of seeds from all of the A. bidwillii trees surveyed. Cockatoos dispersed ca. 30% of the seeds they removed from the mother tree, carrying the seeds to distant perches for handling or dropped them while flying. Dispersal distances ranged between 10 and 153 m (mean = 61m). Most seeds handled for consumption (93%) were fully eaten but others were dropped intact (3%) or only partially eaten (4%), and germination was confirmed for both intact and partially-eaten dispersed seeds. Moreover, seeds dropped by cockatoos facilitated secondary seed dispersal by conspecifics and another three bird species. We found no evidence of other primary dispersal species for A. bidwillii, while the small, winged seeds of A. cunninghamii were just dispersed through barochory and anemochory. The seed weight of the three Araucaria species dispersed by zoochory is strongly related to the body mass of their main seed-dispersing parrot species. These results support a role for parrots as key dispersers of the three large-seeded Araucaria species around the world, and suggest that large seeds may have evolved–at least partially–as an adaptation that allows trees to attract parrots, satiate them, and benefit from their long-distance seed dispersal services.

Highlights

  • Plant investment in reproductive tissues is shaped by biotic and abiotic factors over evolutionary time

  • We showed that the only parrot species living in the monkey puzzle (Araucaria araucana) forests of the Andes, the Austral parakeet (Enicognathus ferrugineus), feeds mostly on the large seeds of this tree during the seeding period, and disperses them at higher rates and for longer distances than do rodents (Tella et al, 2016a)

  • In South America, we found that two other, larger parrot species base their diets on the large seeds (7 g) of the Paraná pine (Araucaria angustifolia) in Atlantic forests, dispersing them at high frequencies and over long distances and more efficiently than the previously recognized bird dispersers (Tella et al, 2016b)

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Summary

Introduction

Plant investment in reproductive tissues is shaped by biotic and abiotic factors over evolutionary time. There was an increase in the amount of cone tissue devoted to seed protection (robust, tightly packed scales) without a concomitant increase in seed size, which has been interpreted as an evolutionary response to the diversification of vertebrate and insect seed predators (Leslie, 2011). These antagonistic plant-animal interactions were combined with climatic factors and mutualistic plantanimal interactions, as seeds are generally larger in animaldispersed than in wind-dispersed conifers (Leslie et al, 2017). Seed size is expected to be constrained by the gape size of those vertebrates (birds and mammals) that could ingest and disperse them, maintaining relatively small propagule sizes (Leslie et al, 2017)

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