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dc.contributor.authorOliveira, Marina Vasconcelos de
dc.date.accessioned2023-12-22T01:49:42Z-
dc.date.available2023-12-22T01:49:42Z-
dc.date.issued2017-02-13
dc.identifier.citationOLIVEIRA, Marina Vasconcelos de. Efeitos dos ninhos de Atta sexdens (Linnaeus, 1758) (Hymenoptera: Formicidae) sobre a estrutura da comunidade de artrópodes do solo na Mata Atlântica. 2017. 27 f. Dissertação (Mestrado em Ciências Ambientais e Florestais) - Instituto de Florestas, Universidade Federal Rural do Rio de Janeiro, Seropédica, 2017.por
dc.identifier.urihttps://rima.ufrrj.br/jspui/handle/20.500.14407/11286-
dc.description.abstractAs florestas tropicais sustentam uma grande diversidade vegetal, em parte, devido à ciclagem de nutrientes iniciada pela fauna de artrópodes do solo, que facilita a ação dos decompositores da serrapilheira, propiciando a liberação dos nutrientes estocados para o solo. Logo, estudos sobre essa fauna e que fatores a afetam são importantes para a compreensão dos processos de ciclagem de nutrientes em florestas tropicais. Dentre os representantes da fauna epigeica, as formigas-cortadeiras são consideradas os herbívoros dominantes da região Neotropical e estudos relatam seus múltiplos efeitos sobre a comunidade vegetal e o solo. Entretanto, não há estudos sobre os efeitos das formigas-cortadeiras sobre a comunidade dos demais artrópodes. Este estudo visa investigar os efeitos dos ninhos de formigas-cortadeiras Atta sexdens (Linnaeus, 1758) (Formicidae: Myrmicinae) sobre a comunidade de artrópodes do solo. A área de estudo foi a Reserva Ecológica de Guapiaçu, município de Cachoeiras de Macacu, Rio de Janeiro, Brasil, na qual coletamos amostras em 10 ninhos de A. sexdens no período de 2 a 9 de fevereiro de 2016. Ao longo de um transecto linear de 32 metros, coletamos amostras de serrapilheira de tamanho 0,25m² a intervalos de 8 metros a partir da borda de cada ninho de A. sexdens, nos quais também medimos as temperaturas do ar e do solo, a luz e a umidade relativa do ar. Objetivamos averiguar se a estrutura da serrapilheira e as condições microclimáticas alteram a estrutura da comunidade de artrópodes e se esses efeitos podem ser mediados pelos ninhos de A. sexdens. As hipóteses em estudo são: 1) Hipótese da Serrapilheira, na qual a estrutura da comunidade de artrópodes seria influenciada pela serrapilheira e a serrapilheira seria alterada por A. sexdens; 2) Hipótese dos Fatores Abióticos, na qual a estrutura da comunidade de artrópodes seria influenciada pelos fatores abióticos locais e estes fatores seriam alterados por A. sexdens e 3) Hipótese do Ninho, em que as alterações na comunidade se dariam por fatores intrínsecos à presença dos ninhos ativos e não explicados por alterações na serrapilheira e/ou nos fatores abióticos medidos. As duas primeiras hipóteses foram testadas através de regressões lineares simples, seguidas de análises de variância, avaliando os efeitos da serrapilheira e dos fatores abióticos sobre os parâmetros da comunidade de artrópodes e se esses efeitos podem ser mediados por A. sexdens. No teste da hipótese do Ninho, fizemos análises de variância e análises de similaridade, avaliando os efeitos diretos de A. sexdens sobre a comunidade dos demais artrópodes. Coletamos 3074 artrópodes, dentre os quais Acari e Collembola foram os grupos mais abundantes. Em relação às formigas, obtivemos 63 morfoespécies, em 26 gêneros e 32 espécies identificadas. O gênero Strumigenys foi um dos gêneros mais frequentes e deteve a maior riqueza dentre os predadores da mirmecofauna. Não detectamos efeitos de A. sexdens sobre a comunidade de artrópodes do solo do seu entorno. Estudos que incluam a sazonalidade e que comparem o comportamento entre diferentes espécies de formigas-cortadeiras podem resultar em novos conhecimentos a respeito da interação desses organismos com os demais artrópodespor
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superiorpor
dc.formatapplication/pdf*
dc.languageporpor
dc.publisherUniversidade Federal Rural do Rio de Janeiropor
dc.rightsAcesso Abertopor
dc.subjectEcosystem engineerseng
dc.subjectAtlantic Foresteng
dc.subjectAttapor
dc.subjectengenheiros de ecossistemaspor
dc.subjectMata Atlânticapor
dc.titleEfeitos dos ninhos de Atta sexdens (Linnaeus, 1758) (Hymenoptera: Formicidae) sobre a estrutura da comunidade de artrópodes do solo na Mata Atlânticapor
dc.title.alternativeNests effects of Atta sexdens (LINNAEUS, 1758) (Hymenoptera:Formicidae) on arthropod community structure of soil in Atlantic Forest.por
dc.typeDissertaçãopor
dc.description.abstractOtherTropical forests support a great vegetal diversity, in part, through an nutrient cycling initiated by the soil arthropod’s fauna, which facilitated the litter decomposers action, propitiating the release of stock nutrients to the soil. Therefore, studies about these fauna and what factors alter it are extremely important to understand the nutrient cycling process in tropical forests. Among epigeic fauna represents, the leaf-cutting ants are considered the Neotropical region dominant herbivores and studies relate their multiple effects on vegetable community and the soil . Nonetheless, there aren’t studies about leaf-cutting ants effects on other arthropods communities, including mirmecofauna. This study aim to investigate the nests effects of the leaf-cutting ant Atta sexdens (Linnaeus, 1758) (Formicidae: Myrmicinae) on a soil arthropod community. The study site was Reserva Ecológica de Guapiaçu, Cachoeiras de Macacu, Rio de Janeiro, Brazil, where we collected samples at ten A. sexdens nests in period of 2 February to 9 February 2016. Along a linear transect of 32 meters, we collected litter samples from 0,25 m² size at intervals of 8 meters from each nests’ edge of A. sexdens, whereby we also measured the air and soil temperature, the light and the air relative humidity. We aim to verify if litter structure and microclimatic conditions alter arthropod community structure and if these effects can be mediated by A. sexdens nests. The hypothesis in question are: 1) Litter Hypothesis, whereby arthropod community structure would be influenced by litter and litter would be altered by A. sexdens; 2) Abiotic Factors Hypothesis, whereby arthropod community structure would be influenced by abiotic factors and these factors would be altered by A. sexdens and 3) Nest Hypothesis, whereby community alterations would happen through intrinsic factors to active nests presence and not explained by alterations in a litter and/or in abiotic factors measured. For the test of the first and the second hypothesis, we did simple regressions and next variance analysis, assessing the litter and abiotic factors effects on arthropod community parameters and if this effects can be mediated by A. sexdens. To test Nest Hypothesis, we did variance analysis and analysis of similarities, assessing direct effects of A. sexdens on other arthropods community. We collected 3074 arthropods, among them Acari and Collembola were the most abundant groups. In relation of the ants, we obtained 63 specimens, in 26 genera and 32 identified species. The Strumigenys genus was one of the most frequent genera and it detained the biggest richness among mirmecofauna predators.We didn’t detect A. sexdens effects on soil arthropod community around its nests. Studies that include sazonality and behavior comparison between different species of leaf-cutting ants can result in new knowledge about the interaction between these organisms and other arthropodseng
dc.contributor.advisor1Queiroz, Jarbas Marçal de
dc.contributor.advisor1ID445.546.641-04por
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/3716769685247180por
dc.contributor.advisor-co1Correia, Maria Elizabeth Fernandes
dc.contributor.advisor-co1ID932.320.637-72por
dc.contributor.advisor-co1Latteshttp://lattes.cnpq.br/8912768268043499por
dc.contributor.referee1Santangelo, Jayme Magalhães
dc.contributor.referee2Rodrigues , Daniela
dc.creator.ID145.178.297-74por
dc.creator.Latteshttp://lattes.cnpq.br/8993267259556871por
dc.publisher.countryBrasilpor
dc.publisher.departmentInstituto de Florestaspor
dc.publisher.initialsUFRRJpor
dc.publisher.programPrograma de Pós-Graduação em Ciências Ambientais e Florestaispor
dc.relation.referencesANTWEB. Disponível em http://www.antweb.org. Acesso em 25 de agosto de 2015. BADEJO, M. A. & AKINWOLE, P. O. Microenvironmental preferences of oribatid mite species on the floor of a tropical rainforest. Experimental and Aplied Acarology, v. 40, p. 145 – 156, 2006. BANG, H. S., LEE, J-H., KWON, O. S., NA, Y. E., JANG, Y. S. & KIM, W. H. Effects of paracoprid dung beetles (Coleoptera: Scarabaeidae) on the growth of pasture herbage and on the underlying soil. Applied Soil Ecology, v. 29, p. 165 – 171, 2005. BESTELMEYER, B. T., AGOSTI, D., ALONSO, L. E., BRANDÃO, C. R. F., BROWN JR., W. L., DELABIE, J. H. C. & SILVESTRE, R. Field techniques for the study of ground-dwelling ants: an overview , description, and evaluation. In: AGOSTI, D., MAJER, J. D., ALONSO, L. E. & SCHULTZ, T. R. Ants: standard methods for measuring and monitoring biodiversity. Smithsonian Institution, Washington, 2000. Cap. 9, p. 122 – 144. BRAGA, R. F., KORASAKI, V., ANDRESEN, E. & LOUZADA, J. Dung beetle community and functions along habitat-disturbance gradient in the Amazon: A rapid assessment of ecological functions associated to biodiversity. Plos One, v. 8, p. 1 – 12, 2013. BURGESS, N. D., PONDER, K. L. & GODDARD, J. Surface and leaf-litter arthropods in the coastal forest of Tanzania. African Journal of Ecology, v. 37, p. 355 – 365, 1999. DECAËNS, T., JIMÉNEZ, J. J., GIOIA, C., MEASEY, G. J. & LAVELLE, P. The values of soil animals for conservation biology. European Journal of Soil Biology, v. 42, p. S23 – S38, 2006. DEL TORO, I., RIBBONS, R. R. & PELINI, S. L. The little things that run the world revisited: a review of ant-mediated ecosystem services and disservices (Hymenoptera: Formicidae). Myrmecological News, v.17, p. 133 – 146, 2012. DELABIE, J. H. C., FISHER, B. L., MAJER, J. D. & WRIGHT, I. W. Sampling effort and choice of methods. In: AGOST, D., MAJER, J. D., ALONSO, L. E. & SCHULTZ, T. R. Ants: standard methods for measuring and monitoring biodiversity. Smithsonian Institution Press, 2000. Cap. 10, p. 145 – 154. DELLA, T. M. C. & SOUZA, D. J. Importância e história de vida das formigas-cortadeiras. In: DELLA, T. M. C. Formigas-cortadeiras: da bioecologia ao manejo. UFV, Viçosa, 2011. Cap.1, p. 13 – 26. DIDHAM, R. K. & SPRINGATE, N. D. Determinants of temporal variation in community structure. In: BASSET, Y., NOVOTNY, V., MILLER S. E. & KITCHING R. L. Arthropods of tropical forests: spatio-temporal dynamics and resource use in the canopy. Cambrigde University Press, New York, 2003. Cap. 4, p. 28 – 39. DONOSO, D. A., JOHNSTON, M. K., CLAY, N. A. & KASPARI,M. Trees as templates for trophic structure of tropical litter arthropod fauna. Soil Biology & Biochemistry, v. 61, p. 45 – 51, 2013. 19 DONOSO, D. A., JOHNSTON, M.K. & KASPARI,M. Trees as templates for tropical litter arthropod diversity. Oecologia, v. 164, p. 201 – 211, 2010. ELO, R. A., PENTTINEN, R. & SORVARI, J. A comparative study of oribatid mite communities in red Wood ant Formica polyctena nests and surrounding soil in a Finnish oak forest. Insect Conservation and Diversity, v. 9, p. 210 – 223, 2016. FARJI-BRENER, A. G. & ILLES, A. E. Do leaf-cutting ant nests make “bottom-up” gaps in neotropical rain forest? : a critical review of the evidence. Ecological Letters, v.3, p. 219 –227, 2000. FARJI-BRENER, A. G. Why are leaf-cutting ants more common in early secondary forests than in old-growth tropical forests? An evaluation of the palatable forage hypothesis. Oikos, v. 92, p. 169 – 177, 2001. FITTKAU, E. J. & KLINGE, H. On biomass and trophic structure of the Central Amazonian rain forest ecosystem. Biotropica, v. 5, p. 2 – 14, 1973. FOLGARAIT, P. J. Ant biodiversity and its relationship to ecosystem functioning: a review. Biodiversity and Conservation, v.7, p. 1221 – 1244, 1998. FORTI, L. C., MOREIRA, A. A., ANDRADE, A. P. P., CASTELLANI, M. A. & CALDATO, N. Nidificação e arquitetura de ninhos de formigas-cortadeiras. In: DELLA, T. M. C. Formigas-cortadeiras: da bioecologia ao manejo. UFV, Viçosa, 2011. Cap.6, p. 102 – 121. GIBB, H. Experimental evidence for mediation of competition by habitat succession. Ecology, v. 92, p. 1871 – 1878, 2011. GOTELLI, N. J. & ELLISON, A. M. Princípios de Estatística em Ecologia. ARTMED, Porto Alegre, 510 p., 2011. HEINIGER, C., BAROT, S., PONGE, J-F., SALMON, S., BOTTOM-DIVET, L., CARMIGNAC, D. & DUBS, F. Effect of habitat spatiotemporal structure on collembolan diversity. Pedobiologia, v. 57, p. 103 – 117, 2014. HENEGHAN, L., COLEMAN, D. C., ZOU, X., CROSSLEY JR., D. A. & HAINES, B. L. Soil microarthropod community structure and litter decomposition dynamics: A study of tropical e temperate sites. Aplied Soil Ecology, v. 9, p. 33 – 38, 1998. HÖLLDOBLER, B. & WILSON, E. O. The Ants. Harvard University Press,USA, 732 p., 1990. HOPP, P. W., OTTERMANNS, R., CARON, E., MEYER, S. ROβ-NICKOLL, M. Recovery of litter inhabiting beetle assemblages during forest regeneration in the Atlantic forest of Southern Brazil. Insect Conservation and Diversity, v. 3, p. 103 – 113, 2010. ILLIG, J., SHATZ, H., SCHEU, S. & MARAUN, M. Decomposition and colonization by micro-arthropods of two litter types in a tropical montane rain forest in southern Ecuador. Journal of Tropical Ecology, v. 24, p. 157 – 167, 2008. JONES, C. G., LAWTON, J. H., & SHACHAK, M. Organisms as Ecosystem Engineer. Oikos, v. 69, p. 373 – 386, 1994. 20 LAVELLE, P. Faunal activities and soil processes: adaptative strategies that determine ecosystem function. Advances in Ecological Research, v. 21, p. 93 – 132, 1997. LEAL, I. R., WIRTH, R. & TABARELLI, M. The multiple impacts of leaf-cutting ants and their novel ecological role in human-modified neotropical forests. Biotropica,v. 0, p. 1 – 13, 2014. LU, J., TURKINGTON, R. & ZHOU, Z-Z. The effects of litter quantity and quality on soil nutrients and litter invertebrates in the understory of two forests in southern China. Plant Ecology, v. 217, p. 1415 – 1428, 2016. LUCKY, A., TRAUTWEIN, M. D.,GUÉNARD, B. S., WEISER, M. D. & DUNN, R. R. Tracing the rise of ants – out of the ground. Plos One, v. 8, p. 1 – 8, 2013. MEHRING, A. S., HATT, B. E., KRAIKITTIKUN, D., ORELO, B. D., RIPPY, M. A., GRANT, S. B., GONZALEZ, J. P., JIANG, S. C., AMBROSE, R. F. & LEVIN, L. A. Soil invertebrates in Australian rain gardens and their potencial roles in storage an processing of nitrogen. Ecological Engeneering, v. 97, p. 138 – 143, 2016. MEYER, S. T., LEAL, I. R. & Wirth, R. Persisting hyper-abundance of leaf-cutting ants (Atta spp.) at the edge of an Old Atlantic forest fragment. Biotropica, v. 41, p. 711 – 716, 2009. MEYER, S. T., LEAL, I. R., TABARELLI, M. & WIRTH, R. Ecosystem engineering by leaf-cutting ants: nests of Atta cephalotes drastically alter forest structure and microclimate. Ecological entomology, v. 36, p. 14 – 24, 2010. MEYER, S. T., NEUBAUER, M., SAYER, E. J., LEAL, I. R., TABARELLI, M. & WIRTH, R. Leaf-cutting ants as ecosystem engineers: topsoil and litter perturbations around Atta cephalotes nests reduce nutrient availability. Ecological Entomology, v. 38, p. 497 – 504, 2013. MILTON, Y. & KASPARI, M. Bottom-up and top-down regulation of decomposition in a tropical forest. Oecologia, v. 153, p. 163 – 172, 2007. MOLOFSKY, J. & AUGSPURGER, C. K. The effect of leaf litter on early seedling establishment in tropical forest. Ecology, v. 73, p. 68-77, 1992. MORAIS, J. W., OLIVEIRA, V. S., DAMBROS, C. S., TAPIA-CORAL, S. C. & ACIOLI, A. N. S. Mesofauna do solo em diferentes sistemas de uso da terra no Alto Rio Solimões, AM. Neotropical Entomology, v. 39, p. 145 – 152, 2010. MOUTINHO, P., NEPSTAD, D.C. & DAVIDSON, E.A. Influence of leaf-cutting ant nests on secondary forest growth and soil properties in Amazonia. Ecology,v. 84, p. 1265 – 1276, 2003. MYERS, N., MITTERMEIER, R. A., MITTERMEIER, C. G., FONSECA, G. A. & KENT, J. Biodiversity hotspots for conservation priorities. Nature, v. 403, p. 853 – 858, 2000. ORGIAZZI, A., BARDGETT, R. D., BARRIOS, E., BEHAN-PELLETIER, V., BRIONES, M. J. I., CHOTTE, J-L., DE DEYN, G. B., EGGLETON, P., FIERER, N., FRASER, T., HEDLUND, K., JEFFERY, S., JONHNSON, N. C., JONES, A., KANDELER, E., KANEKO, N., LAVELLE, P., LEMANCEAU, P., MIKO, L., MONTANARELLA, L., 21 MOREIRA, F. M. S., RAMIREZ, K. S., SCHEU, S., SINGH, B. K., SIX, J., VANDER PUTTEN, W. H. & WALL, D. H. Global Soil Biodiversity Atlas. European Comission, Luxembourg, 176 p., 2016. OTTERMANNS, R., HOPP, P. W., GUSCHAL, M., SANTOS, G. P., MEYER, S. & ROβ-NICKOLL, M. Causal relationship between leaf litter beetle communities and regeneration patterns of vegetation in the Atlantic rainforest of Southern Brazil (Mata Atlântica). Ecological Complexity, v. 8, p. 299 – 309, 2011. PALACIOS-VARGAS, J. G., CASTAÑO-MENESES, G., GÓMEZ-ANAYA, J. A., MARTÍNEZ-YRIZAR, A., MÉJIA-RECAMIER, B. E. & MARTÍNEZ-SÁNCHEZ, J. Litter and soil arthropods diversity and density in a tropical dry Forest ecosystem in Western Mexico. Biodiversity and Conservation, v. 16, p. 3703 – 3717, 2007. RICO-GRAY, V. & OLIVEIRA, P. S. The Ecology and Evolution of Ant-Plant Interactions. University of Chicago Press, London, 320 p., 2007. SAKCHOOWONG, W., HASIN, S., PACKEY, N., AMORNSAK, W.,V BUNYAVEJCHEWIN, S., KONGNOO, P. & BASSET, Y. Influence of leaf litter composition on ant assemblages in lowland tropical rainforest in Thailand. Asia Myrmecology, v. 7, p. 57 – 71, 2015. SANCHES, L., VALENTINI, C. M. A., BIUDES, M. S. & NOGUEIRA, J. S. Dinâmica sazonal da produção e decomposição da serrapilheira em floresta tropical de transição. Revista Brasileira de Engenharia Agrícola e Ambiental, v. 13, p. 183 – 189, 2009. SANDERS, D. & VAN VEEN, F.J.F. Ecosystem engineering and predation: the multi-trophic impact of two ant species. Journal of Animal Ecology, v. 80, p. 569 – 576, 2011. SHULTZ, T.R. & BRADY, S.G. Major evolutionary transitions in ant agriculture. PNAS, v. 105, p. 5435 – 5440, 2008. SILVA, P.S.D., BIEBER, A.G.D., CORRÊA, M.M., & LEAL, I.R. Do leaf-litter attributes affect the richness of leaf-litter ants? Neotropical Entomology, v. 40, p. 542 – 547, 2011. SILVA, R.R. & BRANDÃO, C.R.F. Morphological patterns and community organization in leaf-litter ant assemblages. Ecological Monographs,v. 80, p. 107 – 124, 2010. SORVARI, J., HÄRKÖNEN, S. K. & VESTERINEN, E. J. First record of an indoor pest sawtoothed grain beetle Oryzaephilus surinamensis (Coleoptera: Silvanidae) from wild outdoor wood ant nest. Entomologica Fennica,v. 23, p. 69 – 71, 2012. STAAB, M., SCHULDT, A., ASSMANN, T. & KLEIN, A-M. Tree diversity promotes predator but not omnivore ants in a subtropical Chinese forest. Ecological Entomology, v. 39, p. 637 – 647, 2014. STEPHAN, J.G., WIRTH, R., LEAL, I.R. & MEYER, S.T. Spatially heterogeneous nest-clearing behavior coincides with rain event in the leaf-cutting ant Atta cephalotes (L.) (Hymenoptera:Formicidade). Neotropical Entomology, v. 44, p. 123 – 128, 2015. SUGUITURU, S. S., MORINI, M. S. C., FEITOSA, R. M. & SILVA, R.R. Formigas do Alto Tietê. Canal 6, Bauru, ed.1, 458 p., 2015. TONHASCA JR., A. Ecologia e História Natural da Mata Atlântica. Interciência, Rio de Janeiro, 197 p., 2005. URBAS, P., ARAÚJO JR., M. V., LEAL, I. R. & WIRTH, R. Cutting more from cut forest: edge effects on foraging and herbivory of leaf-cutting ants in Brazil. Biotropica, v. 80, p. 489 – 495, 2007. VARGAS, A. B., MAYHÉ-NUNES, A. J., QUEIROZ, J. M., SOUZA, G. O. & RAMOS, E. F. Efeitos de fatores ambientais sobre a mirmecofauna em comunidades de restinga no Rio de Janeiro, RJ. Neotropical Entomology, v. 36, p. 28 – 37, 2007. VELOSO, H. P., RANGEL FILHO, A. L. R. & LIMA, J. C. A. Classificação da vegetação brasileira, adaptada a um sistema universal. IBGE, Departamento de Recursos Naturais e Estudos Ambiental, Rio de Janeiro, 124 p., 1991. WANG, J., TONG, X. & WU, D. The effect of latitudinal gradient on the species diversity of chinese litter-dwelling thrips. ZooKeys, v. 417, p. 9 – 20, 2014. WIWATWITAYA, D. & TAKEDA, H. Seasonal changes in soil arthropod abundance in the dry evergreen forest of north-east Thailand, with special reference to collembolan communities. Ecological Research, v. 20, p. 59 – 70, 2005.por
dc.subject.cnpqEcologiapor
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dc.originais.urihttps://tede.ufrrj.br/jspui/handle/jspui/1925
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