Biology of Glyphepomis dubia Campos & Souza, 2016 (Hemiptera: Pentatomidae) and the parasitoids Telenomus podisi Ashmead, 1893 and Trissolcus basalis (Wollaston, 1858) (Hymenoptera: Platygastridae) on rice / Biologia de Glyphepomis dubia Campos & Souza, 2016 (Hemiptera: Pentatomidae) e dos parasitoides Telenomus podisi Ashmead, 1893 e Trissolcus basalis (Wollaston, 1858) (Hymenoptera: Platygastridae) em arroz

The life cycle of stink bug, Glyphepomis dubia and the development of two egg parasitoids (Telenomus podisi and Trissolcus basalis) were studied at the Federal University of Maranhão, at 26 ± 2oC, relative humidity (RH) of 60 ± 10% and 12h photophase. Individuals used in the study were collected from seven rice fields located around the municipality of Arari, Maranhão, Brazil, and maintained in greenhouse and laboratory for the life cycle studies. From egg to adult, G. dubia took 35.2 days to complete the life cycle. The oviposition period was 37 days, with egg masses of about 12 eggs each and viability of 93.1%. Longevity was 53 and 65 days for females and males, respectively. The egg parasitoids Te. podisi and Tr. basalis parasitized and developed in G. dubia eggs; however, the biological characteristics of Tr. basalis were affected. Emergence of the parasitoids was higher for Te. podisi (83.5%) compared to the records for Tr. basalis (50.4%). Therefore, G. dubia may potentially achieve a pest status and Te. podisi is a promising biological control agent for G. dubia management in Brazil due to its higher longevity and better reproductive parameters.

O ciclo de vida do percevejo, Glyphepomis dubia e a biologia de dois parasitoides de ovos (Telenomus podisi e Trissolcus basalis) foram estudados na Universidade Federal do Maranhão, a 26 ± 2oC, umidade relativa (UR) de 60 ± 10% e fotofase de 12h. Sete indivíduos de G. dubia foram coletados em lavoura de arroz localizada no município de Arari, Maranhão, Brasil e mantidos em casa de vegetação e laboratório para estudos de ciclo de vida. Do ovo ao adulto, G. dubia levou 35.2 dias para completar o ciclo de vida. O período de oviposição foi de 37 dias com massas de ovos com cerca de 12 ovos/massa e viabilidade de 93.1%. A longevidade foi de 53 e 65 dias, respectivamente, para fêmeas e machos. Os parasitoides de ovos, Te. podisi e Tr. basalis parasitaram e se desenvolveram em ovos de G. dubia, no entanto as características biológicas de Tr. basalis foi afetada. A emergência dos parasitoides foi maior para Te. podisi (83.5%) em comparação com o registrado para Tr. basalis (50.4%). Portanto, G. dubia poderá apresentar potencial para atingir o status de praga e Te. podisi é um promissor agente de controle biológico para ser utilizado no manejo de G. dubia no Brasil, pois apresentou maior longevidade e os melhores parâmetros reprodutivos.

Morphology of the Eggs of Ornithocoris pallidus (Hemiptera, Cimicidae, Haematosiphoninae).

Morphology of cimicid eggs are scarce, and this is the first record for the genus Ornithocoris Pinto, 1927 (Hemiptera: Cimicidae), using scanning electron microscopy (SEM). This genus comprises two species: Ornithocoris toledoi Pinto, 1927 (Hemiptera: Cimicidae) and Ornithocoris pallidus (Usinger, 1959). The eggs of O. pallidus are ellipsoid, and an evident 'lateral flattening', which may give clear asymmetry from the longitudinal axis. The exochorion of the body of the egg and operculum of O. pallidus present spherical or polygonal structures in relief, and pseudomicropyles on the border of the operculum, both differing from Cimex lectularius. The internal face of the operculum is smooth and the border also presented three layers. It was not possible to observe micropyles in the egg of O. pallidus. Bed bugs have a great psychological impact on people, and some people can develop a more or less severe allergic reaction against the bite. Successful control of bed bugs needs serious organization. Studies on egg morphology will add more information to assist in taxonomy studies of O. pallidus and can serve as a basis for control studies because eggs are resistant to insecticides.

New family host and records of Acanthocrios furnarii (Cordero & Vogelsang, 1928) (Hemiptera: Cimicidae) from Argentina, and implications in the transmission mechanism of cimicid bugs among birds' nests.

Acanthocrios furnarii (Cordero & Vogelsang, 1928) [Hemiptera: Cimicidae: Haematosiphoninae] is an ectoparasite on avian hosts from Argentina and Uruguay. It has been mostly found in mud nests of Furnarius rufus (Gmelin, 1788) [Aves: Furnariidae], but its true hosts are some of the inquiline birds that use F. rufus nests. These inquiline hosts belong to the families Emberizidae, Hirundinidae, Icteridae, Passeridae, and Troglodytidae. Outside F. rufus mud nests, A. furnarii has been found in nests of other Furnariidae, Hirundinidae, and Passeridae. The present work adds the first nonpasserine host (Falconidae) of A. furnarii, together with new records in La Pampa, Argentina. The transmission mechanism of A. furnarii, together with all other cimicid bugs from Argentina and adjacent countries, is increased considering this new host; and we also take into account the birds that nidificate in nest boxes, the cavity-nesting birds in trees and earth, and the inquiline birds in stick nests of Furnariidae and Psittacidae.

Ectoparasites in an urban population of big brown bats (Eptesicus fuscus) in Colorado.

Ectoparasites of an urban population of big brown bats (Eptesicus fuscus) in Fort Collins, Colorado, were investigated during summers 2002, 2003, and 2004. Eleven species of ectoparasites were found (the macronyssid mite Steatonyssus occidentalis, the wing mite Spinturnix bakeri, the myobiid mites Acanthophthirius caudata and Pteracarus aculeus, the chirodiscid mite Alabidocarpus eptesicus, the demodicid mite Demodex sp., the chigger Leptotrombidium myotis, the soft tick Carios kelleyi, the batfly Basilia forcipata, the batbug Cimex pilosellus, and the flea Myodopsylla borealis). Five species were analyzed by prevalence and intensity (C. pilosellus, M. borealis, L. myotis, S. bakeri, and S. occidentalis) based on 2161 counts of 1702 marked individual bats over the 3 summer study periods. We investigated 4 factors potentially influencing prevalence and intensity: age class of the host, reproductive status of adult female hosts, roosts in which the hosts were found, and abiotic conditions during the year sampled. The macronyssid mite, S. occidentalis, was the most prevalent and abundant ectoparasite. Adult big brown bats had more ectoparasites than volant juveniles for most of the species analyzed. In a sample of known age bats at 1 large colony, bats of 4 yr of age or greater had higher ectoparasite loads of S. occidentalis and S. bakeri when compared with younger bats. Lactating female bats had the highest prevalence and intensities of most ectoparasites. Annual differences in ectoparasite prevalence and intensity were related to temperature and humidity, which can affect the nidicolous species of ectoparasites. Residents of 2 buildings sprayed insecticides in response to Cimex sp., and this appeared to reduce ectoparasitism of S. occidentalis and C. pilosellus present at these buildings. Intensity of S. occidentalis had no influence on annual survival of big brown bats.

Descrição dos estágios imaturos e biologia de Chinavia pengue (Rolston) (Hemiptera, Pentatomidae) / Description of the immature stages and biology of Chinavia pengue (Rolston) (Hemiptera, Pentatomidae)

Adultos de Chinavia pengue (Rolston, 1983) foram coletados em Garopaba, SC, e criados em laboratório sob condições controladas (24 ± 1°C; UR 70 ± 10 por cento; 12hL:12hE). Como alimento, adultos e ninfas receberam vagens verdes de feijão (Phaseolus vulgaris L.). Os ovos de C. pengue seguem o padrão de coloração e esculturação do cório e coloração e forma dos processos aero-micropilares descrito para as espécies neotropicais de Chinavia. Ninfas de 1° instar possuem uma mancha ovalada no dorso da cabeça e tórax, característica das espécies de Chinavia. Em C. pengue, essa mancha tem coloração laranja-avermelhada, e as manchas abdominais (4+4 manchas laterais e uma mediana) são brancas. Características exclusivas das ninfas de 2° a 5° ínstares de C. pengue são a coloração laranja-avermelhada das manchas do pro- e mesotórax e das manchas circulares no centro das placas abdominais laterais. Não se observou sobreposição nas medidas da largura da cabeça entre os cinco ínstares. Cada fêmea depositou 15,9 ± 4,18 posturas e 218,8 ± 48,60 ovos, sendo 14 ovos/postura o arranjo mais freqüente. A fertilidade foi de 70,0 por cento ± 19,01; a mortalidade no 2° ao 5° estádio foi de 1,6 por cento ± 4,49. A razão sexual obtida foi de 1 macho: 1 fêmea. A duração da fase imatura (ovo a adulto) foi de 45,7 ± 2,99 dias.

Adults of Chinavia pengue (Rolston, 1983) were collected in Garopaba county, SC, and used to establish a laboratory culture under controlled conditions (24 ± 1°C; 70 ± 10 percent RH; 12hL:12hD). Adults and nymphs were fed with green beans (Phaseolus vulgaris L.). Eggs of C. pengue follow the pattern of coloration, chorion sculpture, color and shape of the aero-micropylar processes described to other neotropical Chinavia species. The first instar has the dorsal macula of the head and thorax characteristic of Chinavia species. In C. pengue, this macula is orange-red, and the abdominal maculae (4+4 lateral maculae and one median) are white. From second to fifth instars diagnostic characteristics are orange-red maculae at pro and mesothorax, and at middle of abdominal lateral plates. There was no overlapping of the head-capsule measurements between the five instars of C. pengue. Each female laid an average of 15.9 ± 4.18 egg masses and 218.8 ± 48.60 eggs; there was a marked peak at 14 eggs per egg mass. Mean egg fertility was 70.0 percent ± 19.01; mortality in the second to fifth stadium was 1.6 percent ± 4.49. Sex ratio was 1 male: 1 female. The mean duration of the immature stage (egg to adult) was 45.7 ± 2.99 days.