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Plectus (Ceratoplectus) brzeskii sp. nov. from the Mont Mou, New Caledonia is described and compared with other representatives of the subgenus Ceratoplectus. The new species differs from all species of Ceratoplectus described hitherto by the extremely long rectum (R/ABD = 4.1-4.8 vs. R/ABD < 2.0).
Procamacolaimus dorylaimus sp. nov. is described from the Southern Atlantic (South Shetland Islands, Antarctica). The species is characterised by 3.4-3.5 mm long body; coarsely annulated cuticle without lateral field, epidermal glands and body pores absent, somatic setae present; labial sensilla papilliform, 5.5 µm long cephalic setae; amphid located anteriorly to cephalic setae bases; ocelli absent; deirid and secretory-excretory system absent; stoma 38-41 µm long, strongly cuticularised, spear-like; pharynx heavily muscularized, without radial tubules, valves and bulbs; male reproductive system diorchic; spicules 85.5 µm long, arcuate with ventrally inclined manubrium; gubernaculum complex; 12 tubular supplements, single precloacal setiform sensillum and two subventral postcloacal papilliform sensilla; female reproductive system didelphic, amphidelphic; spermatheca axial, vagina straight; tail conoid, ventrally arcuate; caudal glands present, spinneret small and weakly sclerotized. Procamacolaimus profundus Vitiello, 1974 is transferred to the genus Anguinoides whereas Paraphanolaimus granuliferus Timm, 1963 to Listia. The emended diagnosis, species lists and keys are given for Anguinoides, Procarnacolaimus and Listia.
The phylogeny and classification of the superfamily Plectoidea Örley, 1880 is revised on the basis of published and updated morphological data for 35 ingroup and 2 outgroup species. The following features are here considered to support the monophyletic origin of the superfamily: 1) stegostom developed and differentiated into two sections; 2) dorsal gland orifice opening into the second stegostom section; 3) pharynx cylindrical, with distinct subdivision into corpus and postcorpus by the orifices of the subventral pharyngeal glands and a discontinuity in the muscular pharyngeal tissue; 4) corpus cylindrical, with subdivision into procorpus and metacorpus homologues; 5) pharyngeal radii of the corpus with prominent pharyngeal tubes along the procorpus; 6) cuticular lumen of the basal part of postcorpus (within basal bulb if latter is present) is modified to form a valvular apparatus. In addition the inner labial sensilla open inside the cheilostom. New data on postembryonic development of Anaplectus grandepapillatus (Ditlevsen, 1928), Plectus parietinus Bastian, 1865, P. decens Andrássy, 1985 and P. communis Bütschli, 1873 are given and supplemented with a discussion of the phylogenetic significance of the ontogeny in Plectoidea. Following the proposal of a phylogeny, some key events in the evolution of Plectidae Örley, 1880 are discussed. It is suggested that the superfamily Plectoidea includes four families: Pakiridae Inglis, 1983, Chronogastridae Gagarin, 1975, Metateratocephalidae Eroshenko, 1973 and Plectidae. Plectolaimus supplementatus Keppner, 1988 is transferred to the genus Caribplectus Andrássy, 1973. The genus Keralanema Siddiqi, 2003 is considered a junior synonim of Chronogaster Cobb, 1913. The genus Chiloplectus Andrássy, 1984 is considered a junior synonim of Plectus Bastian, 1865. The family Anaplectidae Zell, 1993 is downgraded to the subfamily level.
The descriptions of Plectus amorphotelus Ebsary, 1985 and P. spicacaudatus Ebsary, 1985 found in Ukraine for the first time are provided. The variability of measurements nine different populations of P. amorphotelus is given. Both species are characterised by atypical structure of tail terminus and absence of caudal glands. New data about distribution of somatic setae and shape of vagina are given. Abnormalities in tail structure in three other species of the genus Plectus are described and discussed.
Wilsonema longicaudatum sp. nov. is described from Biebrzański Park Narodowy, Poland. The new species is characterized particularly in its rather long tail (54.5-62.0 μm, c = 5.5-6.2, c' = 7.0-8.0) and more anterior vulva position (V = 44.2- 45.9%), thus differing from all other species of the genus (ranges for other species: tail is 14-44 μm, c = 7.0-18.5, c' = 2.0-4.5, V = 47.0-56.7%). Moreover, it differs from W. schuurmansstekhoveni in having a shorter rectum (10-11 μm vs 18-28 μm) and higher number of setae in pharyngeal region (six vs four) and tail (five vs four); from W. bangaloreiensis in having a longer body (337-350 μm vs 197-249), lesser number of setae in pharyngeal region (six vs ten) and higher number of setae in the tail (five vs four).
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