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Suspended leaf litter in an understorey treelet as habitat extension for ground-dwelling ants in the Atlantic Forest, south-eastern Brazil

Published online by Cambridge University Press:  22 May 2019

Luiz Eduardo Macedo-Reis*
Affiliation:
Universidade Federal de Minas Gerais, Lab. de Ecologia de Insetos – LEI, Departamento de Genética, Ecologia e Evolução, Belo Horizonte, MG, Brasil
Alice Carvalho Leite
Affiliation:
Universidade Federal de Minas Gerais, Lab. de Ecologia de Insetos – LEI, Departamento de Genética, Ecologia e Evolução, Belo Horizonte, MG, Brasil
Tadeu José Guerra
Affiliation:
Universidade Federal de Minas Gerais, Lab. de Ecologia e Evolução de Plantas Tropicais, Departamento de Botânica, Belo Horizonte, MG, Brasil
Reuber Antoniazzi
Affiliation:
Red de Ecoetología, Instituto de Ecología A.C., Xalapa, Veracruz, México
Frederico de Siqueira Neves
Affiliation:
Universidade Federal de Minas Gerais, Lab. de Ecologia de Insetos – LEI, Departamento de Genética, Ecologia e Evolução, Belo Horizonte, MG, Brasil Department of Biological Sciences, The George Washington University, Washington, DC, USA
*
*Author for correspondence: Luiz Eduardo Macedo-Reis, Email: [email protected]

Abstract

Ground-dwelling ants are active foragers that may extend their foraging area into the vegetation, although the factors affecting their diversity in the suspended litter of understorey plants remain overlooked. To evaluate the influence of the distance between strata, litter biomass and plant size on the ant fauna, the litter ant assemblage of the suspended stratum was compared with the ground immediately below the understorey treelet Erythrochiton brasiliensis (Rutaceae) in an Atlantic Forest, south-eastern Brazil. We collected 1364 ants from 26 ant species. The suspended litter ant assemblage represented a subset of the ground-dwelling ants present in soil litter. The beta diversity results primarily from the high ant species turnover among individual suspended-litter samples, and among ground-litter samples, while species turnover among suspended-ground pairs is lower. Additionally, plant height was not important in determining the species turnover between strata. However, plant height positively correlated with ant species richness, probably because of the increased number of microhabitats. These results suggest that suspended litter in the forest understorey can provide the conditions for ground-dwelling ants to forage and nest, functioning as a vertical extension of resources and microhabitat conditions present in the ground litter.

Type
Short Communication
Copyright
© Cambridge University Press 2019 

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References

Literature cited

Achury, R, Ulloa-chacón, P and Arcila, ÁM (2008) Composición de hormigas e interacciones competitivas con Wasmannia auropunctata en fragmentos de Bosque seco Tropical. Revista Colombiana de Entomología 34, 209216.Google Scholar
Agosti, D and Alonso, LE (2000) The ALL Protocol: a standard protocol for the collection of ground-dwelling ants. In Agosti, D, Majer, JD, Alonso, LE, and Schultz, TR (eds), Ants: Standard Methods for Measuring and Monitoring Biodiversity. Washington, DC: Smithsonian Institution Press, pp. 204206.Google Scholar
Alvares, CA, Stape, JL, Sentelhas, PC, Gonçalves, JLM and Sparovek, G (2013) Köppen’s climate classification map for Brazil. Meteorologische Zeitschrift 22, 711728.CrossRefGoogle Scholar
Armbrecht, I and Ulloa-chacón, P (2003) The Little Fire ant Wasmannia auropunctata (Roger) (Hymenoptera: Formicidae) as a diversity indicator of ants in tropical dry forest fragments of Colombia. Environmental Entomology 32, 542547.CrossRefGoogle Scholar
Armbrecht, I, Perfecto, I and Vandermeer, J (2004) Enigmatic biodiversity correlations: ant diversity responds to diverse resources. Science 304, 284286.CrossRefGoogle ScholarPubMed
Baselga, A (2010) Partitioning the turnover and nestedness components of beta diversity. Global Ecology and Biogeography 19, 134143.CrossRefGoogle Scholar
Brandão, CRF, Silva, RR and Delabie, JHC (2012) Neotropical ants (Hymenoptera) functional groups: nutritional and applied implications. In Panizzi, AR and Parra, JRP (eds), Insect Bioecology and Nutrition for Integrated Pest Management. Boca Raton, FL: CRC Press, pp. 213236.CrossRefGoogle Scholar
Campos, RI, Vasconcelos, HL, Ribeiro, SP, Neves, FS and Soares, JP (2006) Relationship between tree size and insect assemblages associated with Anadenanthera macrocarpa. Ecography 29, 442450.CrossRefGoogle Scholar
Castro, FS, Gontijo, AB, Castro, PDTA and Ribeiro, SP (2012) Annual and seasonal changes in the structure of litter-dwelling ant assemblages (Hymenoptera: Formicidae) in Atlantic semideciduous forests. Psyche 95971.Google Scholar
DaRocha, WD, Neves, FS, Dáttilo, W and Delabie, JHC (2016) Epiphytic bromeliads as key components for maintenance of ant diversity and ant-bromeliad interactions in agroforestry system canopies. Forest Ecology and Management 372, 128136.CrossRefGoogle Scholar
Fernandes, TT, Silva, RRD, Souza, DRD, Araújo, N and Morini, MSDC (2012) Undecomposed twigs in the leaf litter as nest-building resources for ants (Hymenoptera: Formicidae) in areas of the Atlantic Forest in the southeastern region of Brazil. Psyche 2012, 896473.Google Scholar
Foucaud, J, Rey, O, Robert, S, Crespin, L, Orivel, J, Facon, B, Loiseau, A, Jourdan, H, Kenne, M, Masse, PSM, Tindo, M, Vonshak, M and Estoup, A (2013) Thermotolerance adaptation to human-modified habitats occurs in the native range of the invasive ant Wasmannia auropunctata before long-distance dispersal. Evolutionary Applications 6, 721734.CrossRefGoogle ScholarPubMed
Hashimoto, Y, Morimoto, Y, Widodo, ES, Mohamed, M and Fellowes, JR (2010) Vertical habitat use and foraging activities of arboreal and ground ants (Hymenoptera: Formicidae) in a Bornean tropical rainforest. Sociobiology 56, 435448.Google Scholar
Klimes, P, Fibich, P, Idigel, C and Rimandai, M (2015) Disentangling the diversity of arboreal ant communities in tropical forest trees. PLoS ONE 10(2), e0117853.CrossRefGoogle ScholarPubMed
Longino, J and Nadkarni, N (1990) A comparison of ground and canopy leaf litter ants (Hymenoptera: Formicidae) in a neotropical montane forest. Psyche 97, 8193.CrossRefGoogle Scholar
McGlynn, TP, Fawcett, RM and Clark, DA (2009) Litter biomass and nutrient determinants of ant density, nest size, and growth in a Costa Rican tropical wet forest. Biotropica 41, 234240.CrossRefGoogle Scholar
Paoletti, MG, Taylor, RAJ, Stinner, BR, Stinner, DH and Benzing, DH (1991) Diversity of soil fauna in the canopy and forest floor of a Venezuelan cloud forest. Journal of Tropical Ecology 7, 373383.CrossRefGoogle Scholar
Queiroz, ACM, Ribas, CR and França, FM (2013) Microhabitat characteristics that regulate ant richness patterns: the importance of leaf litter for epigaeic ants. Sociobiology 60, 367373.CrossRefGoogle Scholar
Veloso, HP, Filho, ALRR and Lima, JCA (1991) Classificação da Vegetação Brasileira, Adaptada a um Sistema Universal. Rio de Janeiro: IBGE, pp. 124.Google Scholar
Wilkie, KTR, Mertl, AL and Traniello, JFA (2010) Species diversity and distribution patterns of the ants of Amazonian Ecuador. PLoS ONE 5(10), e13146.CrossRefGoogle Scholar