dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorVicente Pereira, Luis Lenin
dc.creatorChaboli Alevi, Kaio Cesar
dc.creatorUrbanin Castanhole, Marcia Maria
dc.creatorFigueiredo Moreira, Felipe Ferraz
dc.creatorBarbosa, Julianna Freires
dc.creatorItoyama, Mary Massumi
dc.date2015-10-21T13:13:39Z
dc.date2016-10-25T21:00:28Z
dc.date2015-10-21T13:13:39Z
dc.date2016-10-25T21:00:28Z
dc.date2015-03-22
dc.date.accessioned2017-04-06T09:01:17Z
dc.date.available2017-04-06T09:01:17Z
dc.identifierJournal Of Insect Science. Cary: Oxford Univ Press Inc, v. 15, p. 1-10, 2015.
dc.identifier1536-2442
dc.identifierhttp://hdl.handle.net/11449/128794
dc.identifierhttp://acervodigital.unesp.br/handle/11449/128794
dc.identifierhttp://dx.doi.org/10.1093/jisesa/iev009
dc.identifierWOS:000352404000004
dc.identifierWOS000352404000004.pdf
dc.identifierhttp://jinsectscience.oxfordjournals.org/content/15/1/21
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/939350
dc.descriptionThe Heteroptera have holocentric chromosomes with kinetic activity restricted to the end of chromosomes. The first meiotic division is reductional for the autosomes and equational for the sexual. Only a few species of this suborder have been analyzed. In this study, we observed the morphologies of the testes of the Heteroptera species Belostoma anurum (Herrich-Schaffer, 1948), Belostoma micantulum (Stal, 1858), Gelastocoris angulatus (Melin, 1929), Gelastocoris flavus flavus (Guerin-Meneville, 1844), Rheumatobates crassifemur crassifemur (Esaki, 1926), Buenoa amnigenus (White, 1879), Buenoa unguis (Truxal, 1953), Martarega brasiliensis (Truxal, 1949), Martarega membranacea (White, 1879), Martarega uruguayensis (Berg, 1883), Rhagovelia tenuipes (Champion, 1898) and Rhagovelia zela (Drake, 1959). We found that the testes of these species can be round, round/spiral, or elongated/spiral. The size of the prophase I cells was found to vary, with the smallest ones being detected in B. micantulum and Rha. zela, the largest in G. f. flavus, and ones of intermediate size in R. c. crassifemur and M. brasiliensis. With respect to the chromosome complement, we verified the presence of 2n = 16 (14A+XY, B. micantulum and G. angulatus), 21 (20A+X0, R. c. crassifemur), 23 (22A+X0, Rha. zela and Rha. tenuipes), 25 (24A+X0, Bu. amnigenus and Bu. unguis; 22A+2m+X0, M. membranacea), 27 (24A+2m+X0, M. brasiliensis and M. uruguayensis), 29 (26A+X1X2Y, B. anurum), and 35 (30A+X1X2X3X4Y, G. f. flavus). We found that the features of spermatogenesis in these species are similar to those of other previously described Heteroptera species, differing only in testicular morphology, chromosome number, and sex chromosome system.
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.languageeng
dc.publisherOxford Univ Press Inc
dc.relationJournal Of Insect Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSpermatogenesis
dc.subjectCytogenetics of heteroptera
dc.subjectTesticular lobe
dc.subjectMeiosis
dc.subjectSpermiogenesis
dc.titleCytogenetics Analysis and Testis Morphology of Aquatic Species of the Families Belostomatidae, Gelastocoridae, Gerridae, Notonectidae, and Veliidae (Heteroptera)
dc.typeOtro


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