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Does masting result in frugivore satiation? A test with Manilkara trees in French Guiana

Published online by Cambridge University Press:  27 August 2015

Irene Mendoza ,
Gabrielle Martin ,
Adeline Caubère ,
Patrick Châtelet ,
Isabelle Hardy ,
Sylvie Jouard  and
Pierre-Michel Forget
Irene Mendoza
Affiliation:
UMR 7179 CNRS-MNHN, Muséum National d'Histoire Naturelle, Département d’Écologie et Gestion de la Biodiversité, 1 Av. du Petit Château, 91800 Brunoy, France Departamento de Botânica, Plant Phenology and Seed Dispersal Research Group, Universidade Estadual Paulista (UNESP), Avenida 24-A no. 1515 – CEP 13506–900, Rio Claro (São Paulo), Brazil
Gabrielle Martin
Affiliation:
UMR 7179 CNRS-MNHN, Muséum National d'Histoire Naturelle, Département d’Écologie et Gestion de la Biodiversité, 1 Av. du Petit Château, 91800 Brunoy, France
Adeline Caubère
Affiliation:
UMR 7179 CNRS-MNHN, Muséum National d'Histoire Naturelle, Département d’Écologie et Gestion de la Biodiversité, 1 Av. du Petit Château, 91800 Brunoy, France
Patrick Châtelet
Affiliation:
CNRS Guyane - USR 3456, 2 rue Gustave Charlery, 97300, Cayenne, French Guiana
Isabelle Hardy
Affiliation:
UMR 7179 CNRS-MNHN, Muséum National d'Histoire Naturelle, Département d’Écologie et Gestion de la Biodiversité, 1 Av. du Petit Château, 91800 Brunoy, France
Sylvie Jouard
Affiliation:
UMR 7179 CNRS-MNHN, Muséum National d'Histoire Naturelle, Département d’Écologie et Gestion de la Biodiversité, 1 Av. du Petit Château, 91800 Brunoy, France
Pierre-Michel Forget*
Affiliation:
UMR 7179 CNRS-MNHN, Muséum National d'Histoire Naturelle, Département d’Écologie et Gestion de la Biodiversité, 1 Av. du Petit Château, 91800 Brunoy, France
*
2 Corresponding author. Email: [email protected]
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Abstract:

Species showing mast seeding synchronously produce large amounts of fruits during some scattered years. This massive crop has been hypothesized to improve dispersal effectiveness by a satiation of seed predators, but the consequences for seed dispersers have barely been studied in the tropics. We tested the hypothesis that masting resulted in satiation of frugivorous dispersers using the study case of two Manilkara species growing in an Amazonian forest in French Guiana. Seed dispersal was estimated by means of seed traps in two forest types during a 10-y monitoring. Manilkara huberi and M. bidentata showed three fruiting events in a time span of 10 y (in 2001, 2006 and 2010). Estimates of seed dispersal from 2001 and 2010 showed that satiation of frugivores only occurred in the year with the largest crop of Manilkara (2010) and in the habitat where the diversity of primate-dispersed species retrieved in seed traps was the highest (Grand Plateau, with clay soils), while fruit consumers did not seem to be satiated in other instances. Spatio-temporal variability of seed production and the community-crop context are therefore affecting satiation of frugivores during masting events.

Keywords

frugivorymass fruitingManilkara huberiManilkara bidentataprimatespredator satiation hypothesisseed dispersalspatio-temporal variation
Type
Short Communication
Information
Journal of Tropical Ecology , Volume 31 , Issue 6 , November 2015 , pp. 553 - 556
Copyright
Copyright © Cambridge University Press 2015 

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Footnotes

1

Contributed equally

References

LITERATURE CITED

CHAUVET, S., FEER, F. & FORGET, P.-M. 2004. Seed fate of two Sapotaceae species in a Guianan rain forest in the context of escape and satiation hypotheses. Journal of Tropical Ecology 20:1–9.Google Scholar
HAMPE, A. 2008. Fruit tracking, frugivore satiation, and their consequences for seed dispersal. Oecologia 156:137–145.Google Scholar
HERRERA, C. M., JORDANO, P., GUITIAN, J. & TRAVESET, A. 1998. Annual variability in seed production by woody plants and the masting concept: reassessment of principles and relationship to pollination and seed dispersal. American Naturalist 152:576–594.Google Scholar
HOWE, H. F. 1980. Monkey dispersal and waste of a neotropical fruit. Ecology 61:944–959.CrossRefGoogle Scholar
JANZEN, D. H. 1971. Seed predation by animals. Annual Review of Ecology and Systematics 2:465–492.CrossRefGoogle Scholar
KELLY, D. & SORK, V. L. 2002. Mast seeding in perennial plants: why, how, where? Annual Review of Ecology and Systematics 33:427–447.Google Scholar
LEVEY, D. J. & BENKMAN, C. W. 1999. Fruit-seed disperser interactions: timely insights from a long-term perspective. Trends in Ecology and Evolution 14:41–43.CrossRefGoogle ScholarPubMed
MAGURRAN, A. E. 2004. Measuring biological diversity. Wiley-Blackwell, Oxford. 260 pp.Google Scholar
NORDEN, N., CHAVE, J., BELBENOIT, P., CAUBERE, A., CHATELET, P., FORGET, P. M. & THEBAUD, C. 2007. Mast fruiting is a frequent strategy in woody species of eastern South America. PLoS ONE 2 (10).CrossRefGoogle ScholarPubMed
NYIRAMANA, A., MENDOZA, I., KAPLIN, B. A. & FORGET, P.-M. 2011. Evidence for seed dispersal by rodents in tropical montane forest in Africa. Biotropica 43:654–657.Google Scholar
PERES, C. A. 1994. Primate responses to phenological changes in an Amazonian terra-firme forest. Biotropica 26:98–112.CrossRefGoogle Scholar
POLANSKY, L. & BOESCH, C. 2013. Long-term changes in fruit phenology in a West African lowland tropical rain forest are not explained by rainfall. Biotropica 45:434–440.Google Scholar
PONCY, O., SABATIER, D., PRÉVOST, M. F. & HARDY, I. 2001. The lowland high rainforest: structure and tree species diversity. Pp. 31–46 in Bongers, F., Charles-Dominique, P., Forget, P.-M. & Théry, M. (eds.). Nouragues: dynamics and plant animal interactions in a Neotropical rainforest. Kluwer, Boston.Google Scholar
RATIARISON, S. 2003. Frugivory in the canopy of a Guianan forest: consequences for seed rain. Ph.D. thesis, Université Pierre et Marie Curie, Paris. 192 pp.Google Scholar
RATIARISON, S. & FORGET, P.-M. 2011. Fruit availability, frugivore satiation and seed removal in two primate-dispersed tree species. Integrative Zoology 6:178–194.Google Scholar
SABATIER, D. 1985. Saisonnalité et déterminisme du pic de fructification en forêt guyanaise. Revue d'Ecologie – La Terre et La Vie 40:289–320.Google Scholar
SAKAI, S. 2002. General flowering in lowland mixed dipterocarp forests of South-east Asia. Biological Journal of the Linnean Society 75:233–247.Google Scholar
SCHUPP, E. W., JORDANO, P. & GOMEZ, J. M. 2010. Seed dispersal effectiveness revisited: a conceptual review. New Phytologist 188:333–353.Google Scholar
SIMMEN, B. & SABATIER, D. 1996. Diets of some French Guianan primates: food composition and food choice. International Journal of Primatology 17:661–693.Google Scholar
STEVENSON, P. R., QUINONES, M. J. & AHUMADA, J. A. 2000. Influence of fruit availability on ecological overlap among four Neotropical primates at Tinigua National Park, Colombia. Biotropica 32:533–544.CrossRefGoogle Scholar
VAN SCHAIK, C. P., TERBORGH, J. W. & WRIGHT, S. J. 1993. The phenology of tropical forests: adaptive significance and consequences for primary consumers. Annual Review of Ecology and Systematics 24:353–377.Google Scholar
WRIGHT, S. J., MULLER-LANDAU, H. C., CALDERON, O. & HERNANDEZ, A. 2005. Annual and spatial variation in seedfall and seedling recruitment in a neotropical forest. Ecology 86:848–860.CrossRefGoogle Scholar
ZUUR, A., IENO, E. N., WALKER, N., SAVELIEV, A. A. & SMITH, G. M. 2009. Mixed effects models and extensions in ecology with R. Springer, New York. 574 pp.CrossRefGoogle Scholar