999 resultados para HYMENOPTERA-APIDAE


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Taeniogonalos raymenti is confirmed as a hyperparasitoid of the tachinid Sturmia convergens which parasitises larval Danaus plexippus. Trigonalids are indirect parasitoids and in this case we have direct evidence that wasp eggs must have been laid on the caterpillar's host plant. Asclepias fruticosa. before the secondary host, but not necessarily before the primary tachinid host, was present. Levels of hyperparasitism during our sampling period were very low at less than two percent.

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The walkeriana species-group of iridescent Euhesma bees is described with the following nine species considered new: E. allunga, E. banksia, E. bronzus, E. dongara, E. lobata, E. spinola, E. sybilae, E. viridescens and E. xana. Two new synonymies are proposed: E. mica (Cockerell) with E. neglectula (Cockerell), and E. halictoides (Rayment) with E. latissima (Cockerell). A key enables the separation of species, and distributions are mapped.

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Morphological studies of development of the egg parasitoid Trichogramma australicum Girault in the cotton bollworm, Helicoverpa armigera (Hubner), were conducted to provide benchmarks for assessing developmental rates in both natural hosts and artificial diets. Observations of living embryos and histological sections show that embryos proceed rapidly through cleavage and blastoderm formation and show a characteristic pinching or rotation 8 h after deposition. Eggs progressively increase in volume, primarily by increasing in diameter at the widest point. At 29 rectangle 1 C the duration of the egg stage is 22-24 h, the larval stage 27 h, the prepupal stage 50-52 h, and pupa 85 h. Larvae undergo dramatic shape changes as they ingest food but do not show signs of larval moults, reinforcing observations that there is only one larval instar. Criteria for staging the embryonic and postembryonic development in natural hosts will be used for future studies aimed at developing and refining artificial diets for Trichogramma.

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Social bees have a diverse fauna of symbiotic mesostigmatic mites, including highly pathogenic parasites of the honeybee, but there are few reports of Mesostigmata phoretic on or inhabiting the nests of solitary or communal, ground-nesting bees. In south-eastern Australia, however, native bees in the family Halictidae carry what appears to be a substantial radiation of host-specific mesostigmatans in the family Laelapidae. Herein, we redescribe the obscure genus Raymentia , associated with Lasioglossum (Parasphecodes ) spp. bees (Halictidae) and describe two new species, R. eickwortiana from L. lacthium (Smith) and R. walkeriana from L. atronitens (Cockerell). The type species, R. anomala Womersley, is associated with L. altichum (Smith). In addition, we review the mites known to be associated with Australian bees, provide a key to differentiate them, and describe and illustrate acarinaria of the Halictinae. We also report on the first occurrences in Australia of the genera Trochometridium Cross (Heterostigmata: Trochometridiidae), from L. eremaean Walker (Halictidae), and Cheletophyes Oudemans (Prostigmata: Cheyletidae) from Xylocopa Latreille (Xylocopinae), and on the previously unknown association between a Neocypholaelaps Vitzthum (Mesostigmata: Ameroseiidae) and Lipotriches tomentifera (Friese) (Halictidae).

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The mating behavior of the quasi-gregarious egg parasitoid Trissolcus basalis (Wollaston) was investigated under field conditions. Trissolcus basalis has female-biased sex ratios and is a protandrous species, with males emerging 1-2 days before females. Males competed aggressively for control of the egg mass, with one male assuming dominance and control of the egg mass, although changes in dominance occurred at least once on each egg mass observed. Typical mating behavior involved the dominant male mating his sisters immediately upon their emergence from the egg mass. These behaviors are characteristic of an inbreeding species that manifests local mate competition. However, several aspects of the mating behavior of T. basalis are inconsistent with that of an inbreeding species. Over 18% of emerging females were not mated by the dominant male upon emergence, 13% of females were not observed to be mated at all and may have left their natal site as virgins, 25% of females were mated multiple times and sometimes by multiple males, females remained near the natal site for up to several hours after emergence before emigrating, and males dispersed away from the natal site during female emergence. Trissolcus basalis may be a predominantly inbreeding species but its emergence and mating behavior suggest that low-frequency outbreeding is also likely to occur.

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Trichogramma australicum larvae develop most rapidly in younger eggs of its host, the pest lepidopteran Helicoverpa armigera . To establish how the developmental stage of the host affects the diet of T. australicum , larvae were fixed in situ in eggs of H. armigera of different ages and the structure of the egg contents and parasitoid gut contents examined histologically. Larvae feeding on newly laid host eggs contain primarily yolk particles in their gut, while larvae feeding on older hosts contain necrotic cells and yolk particles. The gut of T. australicum larvae does not contain organised tissue remnants, indicating that larvae feed primarily by sucking food into their pharynx and feed best on a mixture of particulate semisolids in a liquid matrix. Secretory structures of T. australicum larvae that could be involved in modifying the host environment were examined. The hindgut is modified to form an anal vesicle with a number of attributes suggesting that it may be a specialised secretory structure. The paired salivary glands open to the exterior via a common duct.

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Calyozina dilatata sp.n., from northern Brazil is described and illustrated. This species is recognized by having the fifth foretarsomere dilated. With six scanning micrografies.

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Melanepyris Kieffer, 1913 was proposed to accommodate a single species of Epyris Westwood, 1832, E. imicola Kieffer, 1913, mainly based on the absence of the posterior propodeal carina. Today, Melanepyris includes only two nominal species. The type-material of these species has been considered lost since their original description. In this study, the single known adult male (holotype) of Melanepyris asiaticus Kieffer, 1922 from the Philippines has been rediscovered, redescribed and illustrated. Melanepyris asiaticus is transferred to Epyris Westwood due to the following features: scutellar groove absent, well separated scutellar pits and lower mesopleural fovea large and with undefined upper margin. We checked the original description of M. imicola and concluded that it also fits the definition of Epyris perfectly, except for the (described) absence of a posterior carina. However, the thickness of the posterior carina of the propodeal disc varies within species of different Epyrinae genera. The diagnostic characters used by Kieffer to create Melanepyris and other genera from Epyris are briefly discussed. Melanepyris is proposed as a new junior synonym of Epyris, with the transfer of M. imicola to Epyris.

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Bethylopsis carinatus sp.n., and Epyris chilensis sp.n., from Chile are described and illustrated. Taxonomic data on Chilepyris herbsti Evans, Lytopsenella herbsti (Kieffer), Lytopsenella testaceicornis (Kieffer) and Pseudisobrachium erythrocephalum Evans are included. Male of Lytopsenella herbsti is recorded for the first time to genus and species.

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Diagnosis and genitalia description and illustration of Dissomphalus bicavatusEvans, 1979;D. bispinulatusEvans, 1969;D. brasiliensisKieffer, 1910;Z). caviclypeus Evans, 1969; D. cornutus Evans 1964; D. dumosus, Evans, 1966; D. fungosus Evans, 1979; D. gilvipes Evans, 1979; D. incomptus Evans, 1964; D. infissus Evans, 1969; D. mendicus Evans, 1969; D. microstictus Evans, 1969; D. mirabilis Evans, 1966; D. nanellus Evans, 1969; D. napo Evans, 1979; D. plaumanni Evans, 1964; D. punctatus (Kieffer, 1910); D. puteolus Evans, 1969; D. rufipalpis Kieffer, 1910; D. xanthopus Ashmead, 1893 are provided. Female of D. mirabilis is first described. Five synonymies are proposed: D. connubialis Evans, 1966 of D. brasiliensis, D. montanus Kieffer, 1910 of D. punctatus, D. obliquus Evans, 1979 of D. rufipalpis, D. teren Evans, 1969 of D. cornutus and D. hastatus Evans, 1979 of D. bispinulatus. D. microtuberculatus sp.n. from Northern Argentina is described and illustrated.

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Rhabdepyris longifoveatus sp.n. from southeastern Brazil and R. vesiculosus sp.n. from Central America and northwestern South America are described and illustrated. Rhabdepyris virescens Evans, 1965, R. vesculus Evans, 1065, R. subviridis (Kieffer, 1906), R. violaceus Evans, 1965, R. septemlineatus Kieffer, 1906 and R. lobatifrons Kieffer, 1906 had their sting and male genitalia described.

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Bethylidae specimens from the Reserve were studied in its ecological and faunistic aspects. The material was collected by Malaise and Window traps simultaneously in ten different areas of the Reserve during four years. The total number of genera and specimens were analyzed. Indices of diversity and evenness were used for characterizing the community ecology. Clustering analysis of localities and genera were provided. Nine genera of Bethylidae were found in the Reserve, being Pseudisobrachium Kieffer, 1904 and Apenesia Westwood, 1874 the most common ones. Window trap was more efficient than Malaise trap in terms of genus diversity.

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A survey of Monomachidae species was carried out in anarea of Atlantic rain forest of the Biological Reserve of Duas Bocas, Espírito Santo State, Brazil between September, 1996 and August, 1997. Two species of Mollomachus Klug, 1841, M. fuscator Perty, 1833 and M. eurycephalus Schletterer, 1890 were collected from May to September. Both species are typical of winter time and showed the same parttern of seasonality.

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Apenesia quadrimera sp. n., A. rotunda sp. n. and A. clypeata sp. n. are described and illustrated. New geographic records and variation data of A. cusco Evans, 1966, A distinta Corrêa & Azevedo, 2001, A. funebris Evans, 1963, A. fusilis Corrêa & Azevedo, 2001, A. inca Evans, 1963 and A. transversa Evans, 1963 are added.