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PL
In 1988, we found a large (250–400 × 80–150 μm in protargol preparations) Uroleptus-like hypotrich in a freshwater pond in Harbin, China. We studied the morphology of non-dividers and the cell division using protargol impregnation. Since we disregarded live observations and due to the lack of a modern revision of the uroleptids, a final identification was not possible. A detailed comparison with the most similar limnetic Uroleptus-like hypotrichs and with Rigidothrix goiseri revealed that the Chinese population is very likely identical with Uroleptus magnificus [basionym Holosticha (Paruroleptus) magnificus Kahl, 1932], a very rare species possibly confined to limnetic, stagnant water bodies of the holarctic region. Besides the large size, main features of U. cf. magnificus are: (i) about 80 adoral membranelles; (ii) three or four inconspicuous transverse cirri; (iii) 5–8 dorsomarginal kineties; (iv) the oral primordium originates de novo left of the postoral midventral cirri; (v) the frontal-ventral-transverse cirri anlagen of the proter and the opisthe originate via primary primordia; (vi) the left frontal cirrus of the proter originates from the middle portion of the disorganizing parental paroral; (vii) the parental endoral becomes the undulating membrane anlage for the proter; and (viii) the frontoterminal cirri originate in the plesiomorphic manner, that is, from the rearmost anlage. A compilation reveals that 59 species, subspecies, etc. have been described in or assigned to Uroleptus and Paruroleptus, but only about 50% of them seem to be true uroleptids. Many species of this predominantly limnetic group are little known.
PL
We investigated the status of various Neokeronopsis populations, using protargol-impregnated type material, a new Chinese population, and literature data. This resulted not only in the recognition of a new species, Neokeronopsis asiatica, but also in upgrading Afrokeronopsis from subgenus to genus level. The genera Neokeronopsis and Afrokeronopsis differ mainly in the buccal depression (absent vs. present) and in the midventral cirri between proter and opisthe, which are either retained (Afrokeronopsis) or transformed into cirral anlagen (Neokeronopsis). Neokeronopsis asiatica nov. spec. differs from N. spectabilis (Kahl, 1932) by the following features: body size (~ 300 × 120 μm vs. 400 × 170 μm); posterior body end (acute with distinct indentation at site of caudal cirri vs. broadly rounded and without or indistinct indentation); posterior end of marginal rows (ending at different vs. same or similar level); dorsal kinety 1 (continuous vs. fragmented); and the size of the bases of the adoral membranelles (largest membranelles on average 18 μm vs. 29 μm wide). Improved diagnoses are provided for the family Neokeronopsidae and the genera contained therein, viz., Neokeronopsis, Afrokeronopsis, and Pattersoniella. Our study shows the importance of depositing type and voucher material in recognized repositories. Only this will allow future researchers to restudy the populations, for the sake of improved taxonomic and biogeographic knowledge.
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