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Population structure and canopy use by Coussapoa microcarpa, a strangler hemiepiphyte from the Brazilian Atlantic Forest

Published online by Cambridge University Press:  29 May 2013

Luís Francisco Mello Coelho
Affiliation:
Departamento de Botânica, Instituto de Biociências, Universidade Estadual Paulista Julio de Mesquita, 13506-900, Rio Claro, SP, Brazil Instituto de Pesquisas de Cananéia, 11990-000, Cananéia, SP, Brazil
Marco Aurélio Pizo*
Affiliation:
Departamento de Zoologia, Instituto de Biociências, Universidade Estadual Paulista Julio de Mesquita. 13506-900, Rio Claro, SP, Brazil
*
2Corresponding author. Email: pizo@rc.unesp.br

Abstract:

We studied density, size structure, and establishment sites of Coussapoa microcarpa in the Brazilian Atlantic rain forest. This species is a hemiepiphyte that begins its life in the tops of trees and survives the death of its host to become a free-standing tree. All individuals of C. microcarpa already rooted in the ground were recorded in a 3.43 ha (1.75 ha in lowland and 1.68 ha in submontane) sample of forest plots. Data on total height, root diameter at breast height, host height and diameter at breast height, as well as height, type and diameter of the establishment site were collected. Coussapoa microcarpa present a high density (36.5 ind. ha−1) and the population studied was composed mainly of young individuals. Young and adults differed in establishment sites. The diameter of establishment sites of young was narrower than the diameter of establishment sites of adults, which points out to a limiting factor (diameter of establishment site) regulating the establishment of C. microcarpa.

Type
Short Communication
Copyright
Copyright © Cambridge University Press 2013 

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References

LITERATURE CITED

ATHREYA, V. R. 1999. Light or presence of host trees: which is more important for the strangler fig? Journal of Tropical Ecology 15:589603.CrossRefGoogle Scholar
AVELAR, W. E., GALVãO-BUENO, M. S., GIULIETTI, A. M., FILHO, E. R., ANDRADE-LIMA, D. & GEVERTZ, R. 1995. Em busca do conhecimento ecológico – uma introdução à metodologia. (Second edition). Editora Edgard Blücher Ltda, São Paulo. 113 pp.Google Scholar
BENZING, D. H. 1990. Vascular epiphytes. Cambridge University Press, New York. 354 pp.CrossRefGoogle Scholar
BERG, C. C., AKKERMANS, R. W. A. P. & VAN HEUSDEN, E. C. H. 1990. Cecropiaceae: Coussapoa and Pourouma, with an introduction to the family. Flora Neotropica 51:1128.Google Scholar
BUENO, R. S., GUEVARA, R., RIBEIRO, M. C., CULOT, L., BUFALO, F. S. & GALETTI, M. 2013. Functional redundancy and complementarities of seed dispersal by the last neotropical megafrugivores. PLoS ONE 8: e56252. doi:10.1371/journal.pone.0056252.CrossRefGoogle ScholarPubMed
CAIAFA, A. N. & MARTINS, F. R. 2010. Forms of rarity tree species in the southern Brazilian Atlantic rainforest. Biodiversity and Conservation 19:25972618.CrossRefGoogle Scholar
COELHO, L. F. M. 2005. Ecologia de hemiepífitas estranguladoras. Master's thesis, Universidade Estadual Paulista, Rio Claro, Brazil.Google Scholar
GALETTI, M., PIZO, M. A. & MORELLATO, L. P. C. 2011. Diversity of functional traits in fleshy fruits of a species-rich Atlantic rain forest. Biota Neotropica 11 (1). http://www.biotaneotropica.org.br/v11n1/pt/abstract?article+bn02811012011.CrossRefGoogle Scholar
GAUTIER-HION, A. & MICHALOUD, G. 1989. Are figs always keystone resource for tropical frugivorous vertebrates? A test in Gabon. Ecology 70:18261833.CrossRefGoogle Scholar
HAO, G., SACK, L., WANG, A., CAO, K. & GOLDSTEIN, G. 2010. Differentiation of leaf water flux and drought tolerance traits in hemiepiphytic and non-hemiepiphytic Ficus tree species. Functional Ecology 24:731740.CrossRefGoogle Scholar
HARRISON, R. D. 2006. Mortality and recruitment of hemi-epiphytic figs in the canopy of a Bornean rain forest. Journal of Tropical Ecology 22:477480.CrossRefGoogle Scholar
HOLBROOK, N. M. & PUTZ, F. E. 1996. From epiphyte to tree: differences in leaf structure and leaf water relations associated with the transition in growth form in eight species of hemiepiphytes. Plant Cell and Environment 19:631642.CrossRefGoogle Scholar
JORDANO, P. & HERRERA, C. 1995. Shuffling the offspring: uncoupling and spatial discordance of multiple stages in vertebrate seed dispersal. Ecoscience 2:230237.CrossRefGoogle Scholar
LAWTON, R. O. & WILLIAMS-LINERA, G. 1996. Hemiepiphyte–host relationships: research problems and prospects. Selbyana 17:7174.Google Scholar
MELO, M. M. R. F. & MANTOVANI, W. 1994. Composição florística e estrutura de trecho de mata atlântica de encosta, na ilha do Cardoso (Cananéia, SP, Brasil). Boletim do Instituto de Botânica 9:107158.Google Scholar
MICHALOUD, G. & MICHALOUD-PELLETIER, S. 1987. Ficus hemi-epiphytes (Moraceae) and tree supports. Biotropica 19:125136.CrossRefGoogle Scholar
PUTZ, F. E. & HOLBROOK, N. M. 1986. Notes on the natural history of hemi-epiphytes. Selbyana 9:6169.Google Scholar
SANCHEZ, M., PEDRONI, F., EISENLOHR, P. V. & OLIVEIRA-FILHO, A. T. 2013. Changes in tree community composition and structure of Atlantic rain forest on a slope of the Serra do Mar range, southeastern Brazil, from near sea level to 1000 m of altitude. Flora. doi: 10.1016/j.flora.2013.03.002.CrossRefGoogle Scholar
TODZIA, C. 1986. Growth habits, host tree species, and density of hemiepiphytes in Barro Colorado Island, Panamá. Biotropica 18:2227.CrossRefGoogle Scholar
WILLIAMS-LINERA, G. & LAWTON, R. O. 1995. The ecology of hemiepiphytes in forest canopies. Pp. 255283 in Lowman, M. D. & Nadkarni, N. M. (eds.). Forest canopies. (Third edition). Academic Press, San Diego.Google Scholar