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In the paper the authors present the information on the localities of 77 species of chrysomelid beetles collected in the Podlasie region (after BURAKOWSKI et al. 1990, 1991) in the years 1994-1999. All of them were recorded from that area for the first time.
This paper describes the morphological ultrastructure of the previously unknown final larval instars of the obligate myrmecophilous rove-beetle species Lomeckusa pubicollis. Diagnostic larval characters for the genus Lomechusa are proposed for the first time. At present, this paper is the only up-to-date, detailed and richly illustrated description of the external structures of larvae representing the Lomechusina subtribe. The features of L. pubicollis larvae described here correspond with the abiotic (e.g. absence of ocelh, white body) or biotic conditions (e.g. stumpy body, short legs, absence of urogomphi, dense and asymmetrical chaetotaxy, membranous cuticle) of the anthill, including the passive lifestyle resembling that of the host larvae Formica truncorum, in conjunction with a unique behaviour pattern in the myrmecophileant relationship. Morphological similarities between mature larvae of L. pubicollis and workers of Formica truncorum, the host of this myrmecophile, are also listed. The morphological structure of L. pubicollis larva with the so far best-known larvae of another myrmecophile from the Lomechusini tribe Fella laticollis living in the peripheral zones around the nest, was compared. The different lifestyles of the two species is reflected in the morphological structure of their larvae, particularly: chaetotaxy, structure of setae, ocelli, structure of mouthparts, legs and urogomphi. The characteristics of the morphological structure peculiar to L. pubicollis larva in conjunction with well-developed chemical mimicry, they enable complete adoption and integration in the ant nest, which at such an advanced level appears to be unique compared to other staphylinid myrmecophiles.
The aim of the study was to describe the morphological structure, including chaetotaxy, of the previously unknown early (L₁) and late (L₂₋₃) larval instars of Gyrophaena boleti and to present certain aspects of their behaviour, mainly associated with their means of collecting food. G. boleti is probably the only member of its genus that breeds inside tubes of the open hymenium of the polycarp Fomitopsis pinicola. It was established that certain morphological characters and aspects of the behaviour of the larvae are an expression of the species' adaptation to its preferred host. Thus such characters as body shape, some shortened structures on the head and thorax, the shape of the setae and the length of the urogomphi are the result of synchronic evolution of the larvae with its specific microhabitat, i.e. the narrow tubes of the hymenium. Morphological differences between early and late larval instars of G. boleti involve 17 characters, including 10 new ones that have not previously been noted in gyrophaenines. The level of activity of the tergal gland system varies depending on the age of the larvae, which is probably linked to differences in the structure of the setae on abdominal tergite VIII. The function of these setae was explained for the first time, and a hypothesis was put forth regarding a recognition-aggregation function of tergal gland secretion with respect to individuals within species. The morphological structure of the mature larvae of G. boleti was compared with that of G. nana, which is the only Gyrophaena larva that has been sufficiently well illustrated, and 16 traits differentiating these species were distinguished.
The paper describes and illustrates the morphology of all preimaginal stages for Ocypus fulvipennis Erichson, 1840 including a detailed account of chaetotaxy. Diagnostic characters of egg, larva and pupa of this species are given. Morphological differences between the first (L₁) and mature (L₃) larval instars cover: chaetotaxy of head, profemur, protibia, tarsungulus, abdominal tergites, paratergites, sternites, parasternites and urogomphi; structure of antenna, maxillae and urogomphi; microstructure of abdominal tergites, proportions of the body parts, body colour and habitus. Some data on its distribution and biology in the field and laboratory conditions are also provided. All immature stages of O. fulvipennis were compared with those of other members of this genus. Instead of size, following distinguishing characters are provided for respective stages: egg - tubercle simple, without projection and equatorial band medium in width; larvae (L₃) - teeth of nasale very sharp and well marked, apotome with sharply pointed apex, segment II of labial palp about 2.4 times longer than segment III; pupa - 12 setiform projections on pronotum, antennae distinctly protruding beyond apex of middle tibia, hind legs reaching ⅔ of length of 4th morphological segment.
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