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Adults, and in some species larvae, of several members of Belonuchus Nordmann (Coleoptera: Staphylinidae: Staphylininae) and a few related genera seem to be to various degrees consistently associated with flower bracts of the genus Heliconia (Zingiberales: Heliconiaceae). They are predators and eat various dipterous and lepidopterous larvae in that habitat. Adults of at least Belonuchus cephalotes (Sharp) and Odontolinus fasciatus Sharp are able to immerse completely in water to capture larvae and/or pupae of mosquitoes (Culicidae). Adults and larvae of Belonuchus satyrus Erichson, and adults of B. cacao Blackwelder and B. rufipennis (F.) were found in water-filled flower bracts of Heliconia bihai (L.) L. in northern, lowland Venezuela. The bracts also contained mosquito larvae and semiaquatic coleopterous (Chrysomelidae: Hispinae), lepidopterous (Crambidae: Pyraustinae) and dipterous (Syrphidae, Stratiomyidae, Psychodidae, Richardiidae) larvae, and Annelida. In feeding trials, B. satyrus adults and larvae did not feed on hispine larvae or annelids, but did feed on all the lepidopterous and dipterous larvae available to them; adults dragged larvae and pupae of the mosquito genus Toxorhynchites Theobald from shallow water and thus seemed to be the top predators of the food pyramid within bracts. Records are compiled of association of Belonuchus and relatives with Heliconia bracts in the neotropics. We correct the names used for Heliconia spp. by earlier entomological authors working in Venezuela. Their ‘Heliconia caribaea Lamarck’ is H. bihai (L.) L. and their ‘H. aurea Rodríguez’ is H. bihai cv. Aurea.
We have been surveying a gypsy moth, Lymantria dispar (Lep., Lymantriidae), population in the oak forest of Klingenbach near Eisenstadt, Austria, since 1992. During the last gradation from 1993 to 1996, we studied the natural enemy complex at this site in comparison with other locations where no outbreak occurred (HOCH et al. 2001). During the latency years, an experimental study on the impact of predators on L. dispar pupal populations was performed (GSCHWANTNER et al. 2002). The population density was recorded regularly; in the winter 2001/02, the egg mass surveys indicated a rising population after seven years of latency. We used this opportunity to study the parasitoid complex in the progradation phase. This phase of gypsy moth population dynamics was not studied in our previous work. Moreover, it allowed us to repeat the investigation during the outbreak after 11 years.
A survey of the camerobiid mites living on epiphytic bromeliads and the forest floor of a Mexican tropical dry forest was carried out. We found three new species of the genus Neophyllobius, which are described in this paper; the first two, namely N. cibyci sp. nov. and N. tepoztlanensis sp. nov., were both found inhabiting bromeliads (Tillandsia spp.) and living on two tree species (Quercus obtusata and Sapium macrocarpum); the third, N. tescalicola sp. nov., was found in soil and litter under Q. obtusata. These three new species can be differentiated from other species in the genus by a combination of morphological characters in adult females, mainly those setae on femora and genua I. The idiosoma and leg setal ontogeny of a camerobiid mite is presented for the first time in this paper, illustrating chaetotaxic notations and their relative positions in N. cibyci sp. nov. larva, protonymph and adults (female and male), and establishing setal homologies among instars. Setal homology with other species in the cohort Raphignathina is briefly discussed. Additionally, a compilation and an identification key to all known species of camerobiid mites in Mexico is provided.