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New subgeneric division of Chaetonotus is proposed, mostly basing on reconstruction of cuticular covering evolution. The largest subgenus Euchaetonotus Schwank, 1990 is redefined and its name replaced by Chaetonotus s. sir. The subgenera Bifasciculatella Schwank, 1990 and Diversichaetatella Schwank, 1990 are rejected and three new subgenera Primochaetus, Captochaetus and Marinochaetus are established. New or emended diagnoses of all valid subgenera are given.
The Neotropical species of Rhopobota are listed; nine species (R. larocana sp. .n., R. mostardana sp. n., R. mayarica sp. n., R. ventriloba sp. n., R. monospina sp. n., R. granpiedrae sp. n., R. lacteicaput sp. n., R.cornifera sp. n., R. platyceria sp. n.) are newly described from Cuba and Brazil. Distribution of the genus is mentioned.
Methodological stability in biological nomenclature is being upset recently, with potential consequences for palaeontology. Some systematists, inspired mainly by de Queiroz and Gauthier (1990, 1992, 1994), reject traditional nomenclature in favour of an alternative “Phylogenetic Nomenclature” (PN). Following de Queiroz (2006) I consistently call this Phylogenetic Nomenclature, rather than Phylogenetic taxonomy, as it is often done. Important tenets of PN are the abandonment of hierarchic ranks and binomial names, and establishing name definitions based on cladogram shape (node−, stem−, and stem−modified node−based definitions), apomorphies (apomorphy−based definitions), or a combination of apomorphies and tree topology (apomorphy−modified node−based definition). For an explanation of such definitions, see Cantino and de Queiroz (2003) and Sereno (2005). The practice of Phylogenetic Nomenclature is laid out in an Internet document, the PhyloCode (Cantino and de Queiroz 2003). PN is seen as the natural next step in the evolution of taxonomy: from Linnaeus’ (1753, 1758) “creationist taxonomy” to Hennig’s (1966) cladistic taxonomy. Hence, Linnaeus’ ideas should be removed from nomenclature, which will then reflect phylogeny. Despite the dominance of cladistics as a framework for taxonomy, the validity of its philosophies and methodologies are still questioned (e.g., Szalay 2000). I encourage everyone, independently of school of taxonomy adhered to, to take interest in PN, because: (1) we are all creators or users of taxonomies and classifications, (2) PN is radically different from the current standard, (3) the Preface to the PhyloCode suggests it should ultimately replace the current Codes of Nomenclature (of bacteria, LaPage et al. 1992; of Zoology, ICZN 1999; of Botany, Greuter et al. 2000). I argue herein, why palaeontologists should not follow PN.
For the first time, pollen morphology of 9 (4 spp. and 5 subspp.) taxa representing lobed leaved oaks of Iran in the family of Fagaceae has been examined and illustrated using light microscopy and scanning electron microscopy of acetolysed material. Detailed pollen morphological characteristics are given for Quercus section. The pollen grains are single, isopolar, radially symmetrical, tricolpate, tricolporoidate or tricolporate. Pollens were studied to show all possible characteristics like shape, size, apertures, wall thickness, etc., with special reference to the specific features of each pollen type such as structural, sculptural and suprasculptural patterns. There is considerable variation in pollen morphology between taxa so that, three types of pollen shape, five types of structural pattern, two types of sculptural pattern, five types of suprasculptural pattern and three types of perfora distribution are defined. Furthermore, the relationship between pollen morphology and taxonomy is discussed. Overall, pollen characters are shown to be a useful and informative tool for assessing taxonomic position within Quercus section in Iran.
A new subspecies of the honey badger (Mellivora capensis bu.ech.neri ssp. n.) is described from the western part of Central Asia (Turkmenistan). By the relatively small palatal length it is similar to the subspecies M. c. iridica (Kerr, 1792) and M. c. inaurita {Hodgson, 1838) and differs from them by having larger size and narrower postorbital constriction.
Macholan M., Filippucci M. G., Slivkova L. and Simson S. 1999. Note on the systematic status of shrews of the Sorex araneus group in NW Anatolia. Acta Theriologica 44: 101-106. Although it was assumed that the northern parts of Asia Minor were occupied by the Caucasian shrew, Sorex satunini, some recent findings have cast doubts on the specific status of shrew populations in NW Anatolia. Here, a single shrew from Uludag was studied using enzyme electrophoresis. It was compared to S. araneus from Europe and S. satunini from NE Turkey as well. The results unequivocally classify the animal under study with S. satunini and it is suggested that the common shrew, S. araneus, does not occur either in NW Anatolia or in Asia Minor in general.
Subspecific relationships of the European beaver Castor fiber have been obscured by failure to follow the rules of the International Code of Zoological Nomenclature and remain an open issue. Inconsequence in the use of subspecies names caused a nomen- clatural as well as a taxonomic confusion. We discuss these controversial and incorrect nomenclatural decisions, and recognize 9 nominal subspecies of European beaver, bearing 9 available names: C. f. fiber Linnaeus, 1758, C. f. galliae Geoffroy, 1803, C. f. albicus Matschie, 1907, C. f. vistulanus Matschie, 1907, C. f. pohlei Serebrennikov, 1929, C. f. birulai Serebrennikov, 1929, C. f. tuvinicus Lavrov, 1969, C. f. belorussicus Lavrov, 1981, and C. f. orientoeuropaeus Lavrov, 1981.
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