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Biologia e caracteriza??o morfol?gica de Ornithocoris pallidus (Usinger, 1959) (Heteroptera: Cimicidae: Haematosiphoninae)BASTOS, Amanda Queiroz 30 September 2016 (has links)
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Previous issue date: 2016-09-30 / The cimicidae are distributed in six subfamilies. Among theses Haematosiphoninae has nine genera and Ornithocoris two species: Ornithocoris toledoi Pinto, 1927, for be commonly associated with chickens show economic importance and Ornithocoris pallidus (Usinger, 1959), silvatic associated mainly with swallows. Knowledgment about biology and morphology of this species will contribute to the characterization of taxonomic genus, whose studies are concerning to adult and 5th instar nymphs. Eggs, nymphs and adults were obtained from 10 nests collected in Paula C?ndido municipality (MG), and maintained in laboratory conditions feeding on Mus musculus mice. The study was conducted from established colonies with adults coming from the field. Biological parameters were avaiable (life cycle, number of meal, resistance to starvation and longevity of adults) and morphological of egg and nymphs were observed by optical microscopy (OM) and scanning electron microscopy (SEM). From a total of 2005 eggs, 187 were assigned to the life cycle, 34 and 30 for resistance to starvation and longevity, respectively, and 120 for morphology. Of the 187 nymphs of 1st instar for individualized cycle and number of meal observed, 142 completed the 1st, 88 the 2nd, 80 the 3rd and 76 the 4th instar. The morphometric and chromatic study were performed with 30 eggs (length and width) and 30 nymphs of each instar (total body length and head width of the head with eyes, interocular distance, pronotum height, length pronotal bristle, length of antennal segments of the rostrum and 3rd pair of legs, length and femur width). To the OM study, insects were diaphanized in KOH 10% heated, washed with distilled water, then immersed in acetic acid 1% and mounted between slide and cover slip in alcohol 15%, to observed using optical microscope coupled with a camera lucida. For SEM, the insects were mounted on metal brackets attached with double-sided tape, kept in an oven at 50?C for 24 hours and covered with gold for viewing by scanning electron microscope JEOL JSM 6390 LV - Electron Microscopy Platform Rudolf Barth - FIOCRUZ. The life cycle from egg to adult presented four nymphal instars, at a mean time of 52 ? 10.7 days, performing 0-8 meals, depending on the instar. Males were less resistant to fasting and with less longevity than females, with a mean of 60 ? 19.8 and 66 ? 21.2 and 225 ? 104 and 301 ? 106 days, respectively. The nymphs of 1st and 2nd instars needs more meals and presentes natural mortality, respectively, than the other stages. Among 4th instar, some measured parameters had similar mean to those obtained by Usinger (1966), and eggs of O. pallidus larger than O. toledoi (Carvalho, 1939). As for color, the egg varies from translucent to dark brown; N1 to N3 are light brown and N4 dark brown. By MO, N1 differs from others by having 1 + 1 long bristle at the humeral angle of pronotum, while N2 to N4 have two bristles. SEM, N1 to N4 have a structure at the apex of the 2nd antennal segment, not yet described in the literature, and a ctenidium at the apex of the tibia of the 1st pair of legs also observed by Usinger (1966) in Paracimex capitatus nymphs, Morphological aspects such as the antennas structures that needs further studies, the bristles of pronotum and the presence of ctenidium will provide subsidies to increase the dichotomous key developed by Usinger (1966). The definition of four nymphal instars to O. pallidus corroborate those obtained by Jansen (1979) to O. toledoi, and state that genus Ornithocoris may be characterizate with four nymphal instars. / Os cimic?deos est?o distribu?dos em seis subfam?lias. Dentre estas Haematosiphoninae tem nove g?neros e Ornithocoris possui duas esp?cies: Ornithocoris toledoi Pinto, 1927, por estar comumente associado a galinhas apresenta import?ncia econ?mica e Ornithocoris pallidus (Usinger, 1959), de h?bito silvestre associado principalmente a andorinhas. Conhecer a biologia e morfologia desta esp?cie contribuir? para a caracteriza??o taxon?mica do g?nero, cujos estudos est?o voltados para a forma adulta e ?ltimo est?dio ninfal. Ovos, ninfas e adultos foram obtidos de 10 ninhos coletados no munic?pio de Paula C?ndido (MG), e mantidos em condi??es de laborat?rio, com alimenta??o em camundongos Mus musculus. O estudo foi realizado a partir de col?nias estabelecidas com os adultos procedentes do campo. Foram observados par?metros biol?gicos (ciclo de vida, n?mero de repastos de ninfas, resist?ncia ao jejum e longevidade de adultos) e morfol?gicos de ovo e ninfas pela microscopia ?ptica (MO) e microscopia eletr?nica de varredura (MEV). De um total de 2005 ovos, 187 foram destinados ao ciclo de vida, 34 e 30 para a resist?ncia ao jejum e longevidade, respectivamente, e 120 para a morfologia. Das 187 ninfas de 1? est?dio individualizadas para observa??o do ciclo e n?mero de repastos, 142 completaram o 1?, 88 o 2?, 80 o 3? e 76 o 4? est?dio. Para os estudos morfom?trico e crom?tico foram utilizados 30 ovos (comprimento e largura), e 30 ninfas de cada est?dio (comprimento total do corpo e da cabe?a, largura da cabe?a com os olhos, dist?ncia interocular, altura do pronoto, comprimento da cerda pronotal, comprimento dos segmentos antenais, do rostro e o comprimento e a largura do f?mur do 3? par de pernas. Para o estudo em MO os insetos foram diafanizados em hidr?xido de pot?ssio 10% aquecido, lavados com ?gua destilada, em seguida imersos em ?cido ac?tico 1% e montados entre l?mina e lam?nula em ?lcool 15%, observados em microsc?pio ?ptico, acoplado com c?mara clara para a confec??o dos desenhos. Para a MEV, os insetos foram montados em suportes met?licos presos com fita adesiva dupla face, mantidos em estufa a 50?C por 24 horas e metalizados com ouro para visualiza??o ao microsc?pio eletr?nico de varredura JEOL JSM 6390 LV da Plataforma de Microscopia Eletr?nica Rudolf Barth- FIOCRUZ. O ciclo de vida de ovo a adulto apresentou quatro est?dios ninfais em um tempo m?dio de 52 ? 10,7 dias, realizando de 0 a 8 repastos, dependendo do est?dio. Os machos se mostraram menos resistentes ao jejum e com menor longevidade do que as f?meas, com m?dia de 60 ? 19,8 e 66 ? 21,2, e 225 ? 104 e 301 ? 106 dias, respectivamente. As ninfas de 1? e 2? est?dio apresentaram maior n?mero de repastos e mortalidade natural, respectivamente, do que os demais est?dios. Entre as ninfas de 4?est?dio alguns par?metros mensurados tiveram m?dia similar as obtidas por Usinger (1966), e os ovos de O. pallidus maiores do que os de O. toledoi (Carvalho, 1939; Snipes, 1940). Quanto ? colora??o, o ovo varia de transl?cida a bege escura; de N1 a N3 ? castanho clara e N4 castanho escura. Pela MO, N1 diferencia-se das demais por apresentar 1+1 cerda longa no ?ngulo humeral do pronoto, enquanto que de N2 a N4 existem duas cerdas. Em MEV, de N1 a N4 existe uma estrutura no ?pice do segundo art?culo da antena, ainda n?o descrita na literatura, e um cten?dio no ?pice da t?bia do primeiro par de pernas tamb?m observado por Usinger (1966) em ninfas de Paracimex capitatus. Aspectos morfol?gicos como as estruturas das antenas, que merecem maiores estudos, as cerdas pronotais e a presen?a de cten?dio dar?o subs?dios para incrementar a chave dicot?mica elaborada por Usinger (1966). O encontro de quatro est?dios ninfais para O. pallidus corroboram os obtidos por Jansen (1979) para O. toledoi, e permite afirmar que o g?nero Ornithocoris pode ser cacterizado com quatro est?dios ninfais.
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