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Acrostilicus Hubbard, 1896 and Pachystilicus Casey, 1905 are North American genera known from only one and two species, respectively, and have never been a subject of a modern revision. In fact, Acrostilicus was not even properly described as its author provided only a sketchy diagnosis of the genus and species. Here, we provide a redescription of the genus Acrostilicus and its species and illustrate the habitus and male genital features. For the first time, we also redescribe Pachystilicus and its two species, and provide their differential diagnoses. Additionally, we tested the phylogenetic position of both genera. They were scored into a morphological matrix supplemented with molecular data and the analyses were run using Bayesian inference and maximum likelihood methods. A total of 119 morphological characters and 4859 bp of nuclear (28S, TP, Wg, CADA, CADC, ArgK) and mitochondrial (COI) sequences were analysed for 46 taxa. The results confirmed that both Acrostilicus and Pachystilicus are members of the subtribe Stilicina, but at the same time challenged the monophyly of the subtribe in its current composition. Additionally, we provided further evidence for non-monophyly of the subtribe Medonina and discussed the biology of Acrostilicus and Pachystilicus.
U uvodu rada diferenciraju se morfološka (i „pravomorfološka”) i pravopisna norma, pri čemu se govori i o svojevrsnome paradoksu pravopisne norme. Metodom komparativne i kontrastivne analize u središnjem se dijelu rada raščlanjuju neki relevantni morfološki aspekti koji sudjeluju u definiranju pravopisnih načela i pravopisnih pravila. Cilj je rada osvješćivanje teorijsko-metodoloških aspekata kojima se naznačuju vidovi svojevrsna preklapanja morfologije i pravopisa, i to kroz prizmu hrvatske pravopisne norme, ali i norme nekih slavenskih jezika. U skladu s tim u zaključku se progovara o povezanosti pravopisne norme s morfološkom normom, odnosno kako posebnosti morfološke norme postaju pitanje pravopisne norme.
The genus Trypheridium Brancucci, 1985 is endemic to the Hindu Kush Himalayan Region, and is currently known from a single species, T. nuristanicum (Wittmer, 1956). Here, the genus is reviewed, T. nuristanicum nom. emend. is re-described and T. kashmiricum sp. nov. is described from Kashmir Himalayan Region of India. Descriptions, diagnoses, high quality images, distribution maps and identification keys are presented. The morphology and distribution of Trypheridium are discussed and compared with those of the closely related genus Trypherus LeConte, 1851.
The genus Afronurus has several very common mayfly species in China and they are widely distributed in this country. Some of them are quite similar to each other in both imaginal and nymphal stages. However, these species have not been systematically compared and reviewed so far. In this study, six species are recognized. All nymphs of them share the following characters: gills V–VI with additional arrow-like accessory lobes, branched dentisetae, two rows of bristles and setae on hindtibiae and spotted abdominal terga. The males have divergent penes and clearly expressed titillators. The nymphs of the new species A. drepanophyllus sp. nov. have sickle-like gills I, spotted and striped body color, and males have unique genitalia. The nymphal stages of A. furcatus and A. hunanensis, which are associated and described for the first time, have similar body color to A. drepanophyllus sp. nov., but their pale dots on the head capsules and the shape of the hypopharynx are different. Keys to males and nymphs of the six species are provided.
Pluralization strategies of monolingual German children aged 3-6, median 4;2 (N = 810), and adults aged 18-96, median 24;0 (N = 582), were compared on the basis of eight nonce nouns from the language test SETK 3-5. Differences between younger and older Germans resembled previously described differences between German and immigrant pre-schoolers for most aspects, e.g., use of fewer plural allomorphs (types), more errors in umlauting, and more avoidance strategies in the linguistically weaker groups. However, both German children and adults demonstrated the same universal frequency- and phonology-based pluralization patterns. Surprisingly, ungrammatical plural forms were equally frequent in both children’s and adults' answers.
The taxa of the subgenus Turritus of Cochlostoma (Cochlostomatidae) are analysed based on molecular and morphological data. The phylogenetic trees, based on ribosomal (16S) and nuclear (H3) DNA, indicate that the currently accepted taxonomy should be revised. Based on our data, there are 37 species in Turritus of which 5 are new to science: Cochlostoma (Turritus) pallgergelyi sp. nov., C. (T. ) muranyii sp. nov., C. (T. ) hallgassi sp. nov., C. (T. ) kontschani sp. nov. and C. (T. ) lacazei sp. nov. Of these, we describe the shells and the female genitalia and summarize the distributional data. Some samples (or set of samples) will remain undetermined for lack of data and these are reported in the appendix.
Cochlostoma revised: the subgenus Lovcenia Zallot et al., 2015
(Caenogastropoda, Cochlostomatidae)
(2018)
Five species of the subgenus Lovcenia of Cochlostoma (Cochlostomatidae) are recognized, three of which are described as new to science: C. (L.) tropojanum sp. nov., C. (L.) jakschae sp. nov. and C. (L.) lanatum sp. nov. A lectotype is designated for C. (L.) erika (A.J. Wagner, 1906). The shell and the genital tracts are described for all species and the distributional data are summarized.
Five species of the subgenus Clessiniella of Cochlostoma (Cochlostomatidae) are recognized, viz. Cochlostoma (Clessiniella) villae (Strobel, 1851), Cochlostoma (Clessiniella) tergestinum (Westerlund, 1878), Cochlostoma (Clessiniella) waldemari (A.J. Wagner, 1897), Cochlostoma (Clessiniella) anomphale Boeckel, 1939 and Cochlostoma (Clessiniella) stelucarum sp. nov. The shells and the genitalia are described and the distributional data are summarized for all the species.
A recent paper on the phylogenetic relationships of species within the cephalopod family Mastigoteuthidae meant great progress in stabilizing the classification of the family. The authors, however, left the generic placement of Mastigoteuthis pyrodes unresolved. This problem is corrected here by placing this species in a new monotypic genus, Mastigotragus, based on unique structures of the photophores and the funnel/mantle locking apparatus.
A review of the genus Stratiomys from India is presented. The new species Stratiomys brunettii sp. nov. is described based on male and female specimens collected from the Kashmir Himalayas. The only other congener previously recorded in India, Stratiomys approximata, is redescribed. A key to the species is presented.