Between cultivated and forested environments of the Atlantic Forest: environmental and morphological filters shaping arthropod communities in Heliconia bihai inflorescences
DOI:
https://doi.org/10.1590/2447-536X.v32.e323061Keywords:
Biodiversity conservation, Forest fragments, Functional complementarity, Landscape epidemiology, Ornamental plant, PhytotelmataAbstract
The interplay between cultivated areas and forest fragments creates complex landscapes where ornamental plants such as Heliconia bihai (L.) L., 1763 act as microhabitats linking wild biodiversity to human-modified environments. Our goal was to evaluate how biodiversity, functional structure, and morphological traits influence the arthropod communities associated with H. bihai inflorescences in cultivated and forested environments of the Atlantic Forest. We analysed 344 inflorescences, yielding 14,665 arthropod individuals from 65 morphospecies across cultivated and forested sites. Forest fragments sustained richer and more abundant communities, while cultivated areas hosted mainly generalist taxa, revealing functional complementarity. Diptera dominated both habitats, whereas coleopterans and mites were more representative in forest stands, reflecting the importance of detrital input and structural complexity. Seasonality strongly modulated community composition, with aquatic and semi-aquatic taxa restricted to the rainy season. Community assembly was influenced by interacting microclimatic, seasonal, and morphological filters. These findings demonstrate that biodiversity conservation in cultivated landscapes depends on ecological connectivity between cultivated areas and adjacent forest fragments, which act as reservoirs of specialized taxa and sustain key ecological processes.
Downloads
References
ALMEIDA, N.M.; DIAS, R.F.;ALVES, D.C.V.; MACHADO, S.L.; SILVA, J.D.S.; MELLO, C.F.; ALENCAR, J. Mosquito fauna in phytotelmata across an Atlantic Forest remnant. Frontiers in Ecology and Evolution, v.13, 1525202, 2025. https://doi.org/10.3389/fevo.2025.1525202.
ANTONETTI, D.A.; MALFATTI, E.; UTZ, L.R.P. Influence of environmental and morphological parameters on the microfauna community present in phytotelmata of a bromeliad in a fragment of Atlantic Forest, southern Brazil. Neotropical Biology and Conservation, v.16, n.1, p.59–70, 2021. https://doi.org/10.3897/neotropical.16.e56186.
ARANCIBIA, P.A. The topology of spatial networks affects stability in experimental metacommunities. Proceedings of the Royal Society B: Biological Sciences, v.291, 20240567, 2024. https://doi.org/10.1098/rspb.2024.0567
BENÍTEZ-MALVIDO, J.; DÁTTILO, W.; MARTÍNEZ-FALCÓN, A. P.; DURÁN-BARRÓN, C.; VALENZUELA, J.; LÓPEZ, S.; LOMBERA, R. The multiple impacts of tropical forest fragmentation on arthropod biodiversity and on their patterns of interactions with host plants. PLOS ONE, v.11, n.1, e0146461, 2016. https://doi.org/10.1371/journal. pone.0146461.
BROWN, B.V.; BORKENT, A.; CUMMING, J.M.; WOOD, D.M.; WOODLEY, N.E.; ZUMBADO, M.A. (Eds.). Manual of Central American Diptera. Ottawa: NRC Research Press, 2010.
DENDI, D.; FÖRSTER, T.; CHABOO, C.S. Arthropod diversity in phytotelmata of Calathea capitata (Zingiberales; Marantaceae) host plants from Peru. Revista Peruana de Biología, v.30, n.2, p.1–12, 2023. https://doi.org/10.15381/rpb.v30i2.25654.
LOUNIBOS, L.P.; FRANK, J.H. Insects and allies associated with bromeliads: a review. Terrestrial Arthropod Reviews, v.2, p.163–256, 2009. https://doi.org/10.1163/187498308X414742.
GIONGO, A.; MEDINA-SILVA, R.; ASTARITA, L.V.; BORGES, L.G.A.; OLIVEIRA, R.R.; SIMÃO, T.L.L.; GANO, K.A.; DAVIS-RICHARDSON, A.G.; BROWN, C.T.; FAGEN, J.R.; ARZIVENCO, P.M.; NETO, C.P.; ABICHEQUER, A.D.; LINDHOLZ, C. G.; BAPTISTA- SILVA, A.; MONDIN, C.A.; UTZ, L.R.P.; TRIPLETT, E.W.; EIZIRIK, E. Seasonal physiological parameters and phytotelmata bacterial diversity of two bromeliad species in the Atlantic Forest of Southern Brazil. Diversity, v.11, n.111, 2019. https://doi.org/10.3390/d11070111.
HAYFORD, B.; FÖRSTER, T.; PATEL, V. N.; CHABOO, C. S. Aquatic flies (Diptera) in phytotelmata of Neotropical Zingiberales plants. Journal of Natural History, v.54, p.1–21, 2021. https://doi.org/10.1080/0022293 3.2020.1871522.
HE, S.; WANG, B.; CHEN, K.; SOININEN, J. Patterns in aquatic metacommunities are associated with environmental and trait heterogeneity. Freshwater Biology, v.68, n.1, p.91–102, 2023. https://doi.org/10.1111/fwb.14011.
LEWINSOHN, T.M.; ALMEIDA NETO, M.; ALMEIDA, A.M.; PRADO, P.I.; JORGE, L.R. From insect–plant interactions to ecological networks. Biota Neotropica, v.22, e20221399, 2022. https://doi.org/10.1590/1676- 0611-BN-2022-1399.
MEDEIROS-SOUSA, A.R.; OLIVEIRA-CHRISTE, R.; CERETTI- JUNIOR, W.; BARRIO-NUEVO, K.M.; EVANGELISTA, E.; WILK- DA-SILVA, R.; MUCCI, L.F.; PAULA, M.B.; MARRELLI, M.T. Linking abiotic conditions to mosquito assemblage structure in bromeliads.
Scientific Reports, v.15, 30308, 2025. https://doi.org/10.1038/s41598-025-15514-7.
MÉNDEZ-ROJAS, D.M.; HERNÁNDEZ-LÓPEZ, M.; MARTÍNEZ- FALCÓN, A.P.; RICARTE, A.; LOBATO-GARCÍA, J.M.; BENÍTEZ-MALVIDO, J. Forest type influence on Heliconia–dipteran interaction networks. Insect Conservation and Diversity, v. 18, p. 1–15, 2025. https://doi.org/10.1111/icad.70047.
MÉNDEZ-ROJAS, D.M.; MÁRQUEZ, J.; NAVARRETE-HEREDIA, J.L.; MARTÍNEZ-FALCÓN, A.P.; LOBATO-GARCÍA, J.M.; BENÍTEZ-
MALVIDO, J. Rove beetle species diversity and the patterns of interactions with their host plants in primary and secondary tropical forests. Journal of Insect Conservation, v.28, p.1349–1362, 2024. https://doi.org/10.1007/s10841-024-00633-9.
MISSAGIA, C.C.C.; ALVES, M.A.S. Florivory by phytotelm-breeding insects decreases fecundity in Heliconia (Heliconiaceae). Current Zoology, v.68, n.1, p.195–203, 2022. https://doi.org/10.1093/cz/zoab015.
NAEEM, S. Resource heterogeneity and community structure in Heliconia imbricata phytotelmata. Oecologia, v.84, p.29–38, 1990. https://doi.org/10.1007/BF00665591.
OLIVEIRA, T.R.S.; MOURA, S.R.; CRUZ, D.D.; LOGES, V.; MARTINS, C.F. Interaction and distribution of beetles (Insecta: Coleoptera) associated with Heliconia bihai (Heliconiaceae) inflorescences. Florida Entomologist, v.101, p.160–165, 2018. https://doi.org/10.1653/024.101.0202.
OLIVEIRA, T.R.S.; SENA, D.C.A.; LOGES, V.; CAMARA, C.A.G.; REIS, A.C. Insetos (Arthropoda, Insecta) em inflorescências de Heliconia bihai (L.) L. (Heliconiaceae). Horticultura Ornamental, v.16, n.2, p.174–178, 2010. https://doi.org/10.14295/rbho.v16i2.560.
O’REILLY-BERKELEY, X.; CHAKRABORTY, A.; PATIÑO UYAGUARI, J.L.; MOSSMAN, H.L.; PREZIOSI, R.F.; ROWNTREE, J.K. Effect of genotype on herbivory and growth rate in Heliconia spp. Acta Amazonica, v.55, n.1, 2025. https://doi.org/10.1590/1809-4392202302421.
PROGÊNIO, M.; ANTIQUEIRA, P.A.P.; OLIVEIRA, F.R.; MEIRA, B.R.; LANSAC-TÔHA, F.M.; RODRIGUES, L.C.; ROMERO, G.Q.;
NASH, L.M.; KRATINA, P.; VELHO, L.F.M. Effects of warming on the structure of aquatic communities in tropical bromeliad microecosystems. Ecology and Evolution, v.13, n.2, e9824, 2023. https://doi.org/10.1002/ece3.9824.
SANTOS, V.L.; SILVA, U.C.; SANTOS, E.H.; RESENDE, A.A.; DIAS, M.F.; CUADROS-ORELLANA, S.; MARQUES, A. R. Exploring the
mycobiota of bromeliads phytotelmata in Brazilian Campos Rupestres. Brazilian Journal of Microbiology, v.54, n.3, p.1885–1897, 2023. https://doi.org/10.1007/s42770-023-00977-5.
SEIFERT, R.P. Neotropical Heliconia insect communities. The Quarterly Review of Biology, v.57, p.1–28, 1982.
ŚLIPIŃSKI, S.A.; LESCHEN, R.A.B.; LAWRENCE, J.F. Order Coleoptera Linnaeus, 1758. In: ZHANG, Z.-Q. (Ed.). Animal biodiversity: An outline of higher-level classification and survey of taxonomic richness. Zootaxa, v.3148, p.203–208, 2011. https://doi.org/10.11646/zootaxa.3148.1.39
SOUZA, G.C.S; RIBEIRO, J.E.S.; SOUZA, R.R.; SILVA, R.R.; SOUZA, A.R.; TORO-HERRERA, M.A.; FIGUEREDO, H.F.; FERREIRA, C.P.; BORGES, M.C.R.Z.; PAIVANETO, V.B.; BECKMANN-CAVALCANTE, M.Z. Morphoanatomical and physiological mechanisms of solar irradiation tolerance in heliconia genotypes. Scientia Horticulturae, v.323, 112508, 2024. https://doi.org/10.1016/j.scienta.2024.113511.
TER BRAAK, C.J.F.; ŠMILAUER, P. CANOCO Reference manual and CanoDraw for Windows User’s Guide (Version 4.5). Ithaca: Microcomputer Power, 2002.
WILLIAMS, D.D. The Biology of Temporary Waters. Oxford: Oxford University Press, 2006.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Thais Ranielle Souza de Oliveira, Vivian Loges, Denise Dias da Cruz, Celso Feitosa Martins

This work is licensed under a Creative Commons Attribution 4.0 International License.





