116 research outputs found

    Co-existence Of Ants And Termites In Cecropia Pachystachya Trécul (urticaceae)

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    Individuals of Cecropia pachystachya Trécul (Urticaceae) host Azteca (Hymenoptera: Formicidae) colonies in their hollow internodes and feed them with glycogen bodies produced in modified petiole bases (trichilia). In turn, ants keep trees free from herbivores and lianas. Here, we report for the first time the association of nests of Nasutitermes ephratae Rambur (Isoptera: Termitidae) with these trees, in South-Pantanal (Brazil). We aimed to describe the Cecropia-ant-termite relationship and to investigate how their coexistence is made possible. We hypothesize that: 1) The frequency of termite nests in C. pachystachya is lower than in neighbor trees; 2) Termite nests occur in trees with lower density of foraging ants; 3) The time that ants take to find and remove live termite baits in C. pachystachya trees is lower in leaves (close to trichilia) than in trunks; 4) Termite nests are fixed preferentially in the smallest and less branched trees; and 5) Termite nests are fixed preferentially distant from the canopies. Unexpectedly, termitaria occurred in C. pachystachya at the same frequency as in other tree species; there was no relationship between ant patrol activity and the occurrence of termite nests in C. pachystachya; and they occurred mainly in the tallest and more branched trees. However, termite nests generally were fixed in the trunk, fork or basal branches, where there is better physical support and ant patrol is more modest. The segregation of termite and ant life-areas may represent a escape strategy of termites in relation to ants inhabiting C. pachystachya, specially during nest establishment. The isolation of termites in fibrous nests and galleries may complete their defense strategy.6118894Agrawal, A.A., Leaf damage and associated cues induce aggressive ant recruitment in a neotropical ant-plant (1998) Ecology, 79, pp. 2100-2112Agrawal, A.A., Dubin-Thaler, B.J., Induced Responses to Herbivory in the Neotropical Ant-Plant Association between Azteca Ants and Cecropia Trees: Response of Ants to Potential Inducing Cues (1999) Behavioral Ecology and Sociobiology, 45, pp. 47-54Alho, C.J.R., Gonçalves, H.C., (2005) Biodiversidade Do Pantanal: Ecologia e Conservação, p. 135. , Campo Grande: Editora UniderpBerg, C.C., Rosselli, P.F., Davidson, D.W., (2005) Flora Neotropica: Cecropia, 94, p. 236. , New York: New York Botanical Garden PressBraekman, J.C., Daloze, D., Dupont, A., Pasteels, J.M., Le-Feuve, P., Borderau, C., Declercq, J.P., Van Meerssche, M., Chemical composition of the frontal gland secretion from soldiers of Nasutitermes lujae (Termitidae: Nasutermi-tinae) (1983) Tetrahedron, 39, pp. 4237-4241Carroll, C.R., Janzen, D.H., Ecology of foraging by ants (1973) Annual Review of Ecology and Systematics, 4, pp. 231-257Cunha, H.F., (2000) Estudo de Colônias de Constrictotermes Cyphergaster (Isoptera, Termitidae: Nasutitermitinae) No Par-que Estadual da Serra de Caldas Novas, GO, p. 51. , Dissertação de mestrado, Univ. Federal de Goiás, Instituto de Ciências Bio-lógicas/DBG, GoiâniaDavidson, D.W., Fisher, B.L., Symbiosis of ants with Cecropia as a function of light regime (1991) Ant-Plant Interactions, pp. 289-309. , Huxley, C. & Cutler, D. K. (eds.), New York: Oxford University PressDavidson, D.W., McKey, D., The evolutionary ecology of symbiotic ant-plant relationships (1993) Journal of Hymenoptera Research, 2, pp. 13-83Dejean, A., Fénéron, R., Predatory behaviour in the ponerine ant, Centromyrmex bequaerti: A case of termitolesty (1999) Behavioural Processes, 47, pp. 125-133Dejean, A., Grangier, J., Leroy, C., Orivel, J., Preda-tion and aggressiveness in host plant protection: A generalization using ants of the genus Azteca (2009) Naturwissenschaften, 96, pp. 57-63Delabie, J.H.C., Inquilinismo simultâneo de duas es-pécies de Centromyrmex (Hymenoptera: Formicinae: Pone-rinae) em cupinzeiros de Syntermes sp. (Isoptera: Termitidae: Nasutiterminae) (1995) Revista Brasileira de Entomologia, 39, pp. 605-609Downhower, J.F., The distribution of ants on Cecropia leaves (1975) Biotropica, 7, pp. 59-62Eisner, T., Kriston, I., Aneshansley, D.J., Defensive Behavior of a Termite (Nasutitermes exitiosus) (1976) Behavioral Ecology and Sociobiology, 1, pp. 83-125Folgarait, P.J., Johnson, H.L., Davidson, D.W., Responses of Cecropia to experimental removal of mullerian bodies (1994) Functional Ecology, 8, pp. 22-28Gonçalves, T.T., Reis, R., Desouza, O., Ribeiro, S.P., Predation and interference competition between ants (Hymenoptera: Formicidae) and arboreal termites (Isoptera: Termitidae) (2005) Sociobiology, 46, pp. 409-419Higashi, S., Ito, F., Defense of termitaria by termito-philous ants (1989) Oecologia, 80, pp. 145-147Hölldobler, B., Wilson, E.O., (1990) The Ants, p. 732. , Berlin: Harvard University PressJanzen, D.H., Coevolution of mutualism between ants and acacias in Central America (1966) Evolution, 20, pp. 249-275Janzen, D.H., Allelopathy by myrmecophytes: The ant Azteca as an allelopathic agent of Cecropia (1969) Ecology, 50, pp. 147-153Janzen, D.H., Dissolution of mutualism between Cecropia and its Azteca ants (1973) Biotropica, 5, pp. 15-28Lemaire, M., Lange, C., Lefevre, J., Clement, J.L., Stra-tegie de camoufage du prédateur Hypoponera eduardi dans les sociétés de Reticulitermes européens (1986) Actes Coll. Insectes So-ciaux., 2, pp. 97-101Longino, J.T., Azteca ants in Cecropia trees: Taxonomy, colony structure and behaviour (1991) Ant-Plant Interactions, pp. 198-212. , Cutler, D. F. & C. R. Huxley (eds.), New York: Oxford University PressNoirot, C., Darlington, J.P.E.C., Termites nests: Architecture, regulation and defence (2000) Termites: Evolution, Sociality, Symbioses, Ecology, pp. 121-139. , Abe, T., et al. (eds.), Dordrecht: Kluwer Academic PublishersOliveira, P.S., Oliveira-Filho, A.T., Cintra, R., Ant foraging on ant-inhabited Triplaris (Polygonaceae) in western Brazil: A feld experiment using live termite-baits (1987) Journal of Tropical Ecology, 3, pp. 193-200Pott, A., Pott, V.J., Plantas do Pantanal (1994) Brasília: Embrapa-SPI, p. 320Putz, F.E., Holbrook, N.M., Further observations on the dissolution of mutualism between Cecropia and its ants: The Malaysian case (1988) Oikos, 53, pp. 121-125Quinet, Y., Tekule, N., Biseau, J.C., Behavioural interactions between Crematogasterbrevispinosa rochai Forel (Hymenoptera: Formicidae) and two Nasutitermes species (Isoptera: Termitidae) (2005) Journal of Insect Behavior, 18, pp. 1-17. , doi: 10.1007/s10905-005-9343-yRico-Gray, V., Oliveira, P.S., (2007) The Ecology and Evolution of Ant-plant Interactions, p. 320. , Chicago: University of Chicago PressRickson, F.R., Glycogen plastids in Müllerian body cells of Cecropia peltata-a higher green plant (1971) Science, 173 (3994), pp. 344-347. , doi: 10.1126/science.173.3994.344Sagers, C.L., Ginger, S.M., Evans, R.D., Carbon and nitrogen isotopes trace nutrient exchange in an ant-plant mutualism (2000) Oecologia, 123, pp. 582-586Sheppe, W., Invertebrate predation on termites of the African savanna (1970) Insectes Sociaux, 17, pp. 205-218Schupp, E.W., Azteca protection of Cecropia: Ant occupation benefts juvenile trees (1986) Oecologia, 70, pp. 319-385Soriano, B.M.A., Oliveira, H., Catto, J.B., Comastri-Filho, J.A., Galdino, S., Salis, S.M., (1997) Plano de Utilização da Fazenda Nhumirim (Documento 21), p. 72. , http://www.cpap.embrapa.br/publicacoes/online/DOC21.pdf, Corumbá: Embrapa-CPAP, (accessed date: 12 November, 2013)Thorne, B.L., Diferences in nest architecture between the neotropical arboreal termites Nasutitermes corniger and N. Ephrateae (Isoptera, termitideae) (1980) Psyche, 87, pp. 235-244Thorne, B.L., Haverty, M.I., Nest growth and survivorship in three species of neotropical Nasutitermes (Isoptera: Termitidae) (2000) Environmental Entomology, 29, pp. 256-264Vasconcelos, H.L., Casimiro, A.B., Infuence of Azteca alfari ants on the exploitation of Cecropia trees by a leaf-cutting ant (1997) Biotropica, 29, pp. 84-92Vasconcellos, A., Moura, F.M.S., Wood litter consumption by three species of Nasutitermes termites in an area of the Atlantic Coastal Forest in northeastern Brazil (2010) Journal of Insect Science, 10, p. 72. , http://insectscience.org/10.72/Vieira, A.S., Faccenda Antonialli-Junior O, W.F., Fernandes, W.D., Nest structure and occurrence of three species of Azteca (Hymenoptera, Formicidae) in Cecropia pachystachya (Urticaceae) in non-foodable and foodable pantanal areas (2010) Revista Brasileira de Entomologia, 54, pp. 441-445. , doi: 10.1590/S0085-56262013000100013Weber, N.A., Termite prey of some African ants (1964) Entomological News, 75, pp. 197-204Wheeler, W.M., Ecological relations of ponerinae and other ants to termites (1936) Proceedings of the American Academy of Arts and Science, 71, pp. 159-243Wheeler, W.M., Studies of neotropical ant-plants interactions ant their ants (1942) Bulletin of the Museum of Comparative Zoology Harvard, 90, pp. 1-262Wilson, E., (1971) The Insect Societies, p. 560. , Cambridge: Belknap Press of Harvard University Pres

    Velocity-space sensitivity of the time-of-flight neutron spectrometer at JET

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    The velocity-space sensitivities of fast-ion diagnostics are often described by so-called weight functions. Recently, we formulated weight functions showing the velocity-space sensitivity of the often dominant beam-target part of neutron energy spectra. These weight functions for neutron emission spectrometry (NES) are independent of the particular NES diagnostic. Here we apply these NES weight functions to the time-of-flight spectrometer TOFOR at JET. By taking the instrumental response function of TOFOR into account, we calculate time-of-flight NES weight functions that enable us to directly determine the velocity-space sensitivity of a given part of a measured time-of-flight spectrum from TOFOR

    Relationship of edge localized mode burst times with divertor flux loop signal phase in JET

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    A phase relationship is identified between sequential edge localized modes (ELMs) occurrence times in a set of H-mode tokamak plasmas to the voltage measured in full flux azimuthal loops in the divertor region. We focus on plasmas in the Joint European Torus where a steady H-mode is sustained over several seconds, during which ELMs are observed in the Be II emission at the divertor. The ELMs analysed arise from intrinsic ELMing, in that there is no deliberate intent to control the ELMing process by external means. We use ELM timings derived from the Be II signal to perform direct time domain analysis of the full flux loop VLD2 and VLD3 signals, which provide a high cadence global measurement proportional to the voltage induced by changes in poloidal magnetic flux. Specifically, we examine how the time interval between pairs of successive ELMs is linked to the time-evolving phase of the full flux loop signals. Each ELM produces a clear early pulse in the full flux loop signals, whose peak time is used to condition our analysis. The arrival time of the following ELM, relative to this pulse, is found to fall into one of two categories: (i) prompt ELMs, which are directly paced by the initial response seen in the flux loop signals; and (ii) all other ELMs, which occur after the initial response of the full flux loop signals has decayed in amplitude. The times at which ELMs in category (ii) occur, relative to the first ELM of the pair, are clustered at times when the instantaneous phase of the full flux loop signal is close to its value at the time of the first ELM

    New insights into the genetic etiology of Alzheimer's disease and related dementias

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    Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele
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