Among the results of Russian influence on Czech in the 19th century was the emergence of an active past participle in -(v)ší in Czech. Although not welcomed by all grammarians, this participle continued its existence in Czech until today, becoming mainly a device of archaic and bookish style. In the actual work, the occurence oft the active past participle in -(v)ší in the largest partial corpus of the Czech National Corpus containing journalistic texts is studied. A main result of the study is that apart from a large number of examples from different verbs which show the active past participle on -(v)ší in the studied corpus once or twice and where it is indeed a device of archaic and bookish style, sometimes even of irony and humor, there is a small group of (mainly intransitive) verbs, where this participle functions with considerable frequency in stylistically more neutral contexts of written Standard Czech as the only participle (sometimes as a - stylistically more marked - variant of a more numerous active past participle in -l). In theses cases, it remains overwhelmingly a syntactically unextended direct attribute of a noun. Such active past participle in -(v)ší is to be found most often in sports coverage where it is built from a set of verbs with terminological function.
Phonochorion Uvarov (Orthoptera: Tettigoniidae: Phaneropterinae) is a little known genus consisting of three species: Ph. satunini, Ph. artvinensis and Ph. uvarovi. The objective of this study is to conduct a thorough distributional, taxonomic and systematic revision of the genus Phonochorion using both bioacustic and external morphological characters. Field surveys indicate that the genus is distributed from the Trabzon region of Turkey to the Khulo province of Georgia however the exact limit of the eastern distribution of the genus remains unknown. Phonochorion species occur only on the northern slopes of the East Black Sea and Lesser Caucasus Mountains. The Coruh Valley, which seprates the East Black Sea and Lesser Caucasus Mountain ranges, seems to be an effective physical and climatic barrier and determines the distribution of these species. Ph. uvarovi can clearly be distinguished from Ph. satunini and Ph. artvinensis by the calling songs of males and external morphological characters. Ph. artvinensis and Ph. satunini differ in several taxonomic characters but the males have virtually identical calling songs. From a character evolution perspective, although geographically more distant, Ph. satunini is more closely related to Ph. uvarovi than Ph. artvinensis. Morphological similarities in several characters indicate Phonochorion to be most closely related to Polysarcus zacharovi and the Poecilimon heroicus-group. Within the genus Phonochorion, song structure and morphological characters clearly indicate Ph. uvarovi to be the basal taxon.
The species Beludzhia phylloteliptera Rohdendorf is redescribed from adult males and females as well as all larval instars collected in the United Arab Emirates. The morphology of the first instar larva is strikingly similar to that of Dolichotachina marginella (Wiedemann) and Phylloteles pictipennis Loew, all of which are here documented for the first time. These three generic representatives share several character states, which are probably plesiomorphic relative to the condition observed in other miltogrammine larvae, but the uniquely shaped, slender mouthhook, a cushion- or pad-like lobe behind the maxillary palpus (cheek organ), the antero-ventral segmental prolegs of the first instar larva, and the integumental warts of the third instar larvae, are shared character states not known from any other species of Sarcophagidae. Beludzhia Rohdendorf is therefore placed with Dolichotachina Villeneuve and Phylloteles Loew in the tribe Phyllotelini.
A phylogenetic analysis of the four coleopteran suborders (Polyphaga, Archostemata, Myxophaga and Adephaga), four other endoneopteran taxa (Strepsiptera, Neuropterida, Mecopterida and Hymenoptera) and three neopteran outgroups (Orthoneoptera, Blattoneoptera and Hemineoptera) is performed based on 63 characters of hind wing venation, articulation and folding patterns, with character states coded for the groundplan of each taxon (not for exemplar genera or species). The shortest tree found using Winclada with Nona exhibits the following topology: Orthoneoptera + (Blattoneoptera + (Hemineoptera + Endoneoptera: (Hymenoptera + ((Neuropterida + Mecopterida) + (Coleoptera + Strepsiptera))))). Homologization of the hind wing venation in Coleoptera is reviewed and updated, and comments are made concerning recent works on wing folding. Recent phylogenetic schemes proposed for the orders of Endoneoptera and suborders of Coleoptera are reviewed and their supporting evidence critically examined. The special role and influence of the hind wing anojugal lobe on the diversification of Neoptera and Endoneoptera is discussed. A scenario is proposed for the origin and evolution of the insect hind wing.
This paper presents a synthesis of morphological information on larvae of the beetle suborder Archostemata. Larvae of the following families and species were studied: Ommatidae: Omma sp.; Micromalthidae: Micromalthus debilis LeConte, 1878; Cupedidae: Priacma serrata LeConte, 1861, Distocupes varians (Lea, 1902), Rhipsideigma raffrayi (Fairmaire, 1884), Tenomerga cinerea (Say, 1831) and Tenomerga mucida (Chevrolat, 1829). Morphological characters of the suborder and three families are described. Monophyly of the suborder is strongly supported by more than 10 larval autapomorphies. A close relationship between Micromalthidae and Cupedidae is confirmed. New larval characters are introduced, including chaetotaxy of first instar larvae of Micromalthus LeConte, 1878, Priacma LeConte, 1874 and Distocupes Neboiss, 1984. An identification key to families and subfamilies of Archostematan larvae is provided, along with a checklist of extant Archostemata taxa. The work is illustrated with 120 morphological drawings.
The Oriental helotrephid genus Idiotrephes Lundblad, 1933, is taxonomically revised. Species discrimination is based on male genitalia and female terminalia. Three species groups are recognized. The I. chinai group contains I. chinai Lundblad, 1933 (type species; from Sumatra, Borneo, and West Malaysia) and three newly described species; I. asiaticus sp. n. (from Vietnam, Thailand, and west Malaysia); I. yupae sp. n., and I. polhemusi sp. n. (both from Thailand). The I. maior group contains I. maior Papáček, 1994; I. meszarosi Papáček, 1995 (both from Vietnam), and I. hainanensis sp. n. (from Hainan, China). The I. thai group consists of two newly described species from north and northeast Thailand, I. thai sp. n. and I. shepardi sp. n. In addition, some features of biology and morphology of the ovipositor are also included.
The Poecilimon ornatus group has an exclusively European distribution and includes the largest species in the genus. A revision of the taxa belonging to this group in Bulgaria and Macedonia (Central and Eastern Balkan Peninsula) is presented. Nine taxa described from Bulgaria are synonymised with 3 previously known species, as follows: Poecilimon ornatus (= P. mistshenkoi marzani, syn. n., P. mistshenkoi tinkae, syn. n., P. mistshenkoi vlachinensis, syn. n.), P. affinis s. str. (= P. mistshenkoi mistshenkoi, syn. n., P. affinis ruenensis, syn. n., P. affinis rilensis, syn. n., P. affinis medimontanus, syn. n., P. harzi, syn. n.) and P. hoelzeli (= P. kisi, syn. n.). The synonymy of P. poecilus with P. affinis and the subspecific status of P. affinis komareki are confirmed. One species, Poecilimon jablanicensis, sp. n., is described as new to science. A tabulated key, lists and maps of all known localities and oscillograms of the songs of all the species in this group are presented. The phylogenetic relationships and evolutionary trends in the Poecilimon ornatus group are discussed.
The long-time process of paradigm levelling in the present-tense third-person plural of the IV-verb-class has been in progress since the 17th century at least. The aim of this paper is to describe how the concurrence between the standard (prosí, trpí, sázejí) and non -standard forms (in particular prosejí/trpějí and sází) manifested itself in the works by Bohumil Hrabal (1914-1997). The inquiry into Hrabal‘s selected works (the sample contains 20 works written between 1938 and 1995) proves a context-bound prosejí/trpějí incidence as well as a rather less frequent incidence of the sází form.
In this paper a combination of characters by which Poecilimon species (Orthoptera: Tettigonioidea: Phaneropteridae) can be recognised as members of the P. sanctipauli group are described. Most important are the wide fastigium, short ovipositor and song characters. The morphological characters are figured and described (Table 1), and the song patterns illustrated by oscillograms. The proposed phylogenetic relationships of the members of this group are written as [P. mytilenensis (P. pulcher, P. lodosi, P. sanctipauli)]. All species of the group are known from southwest Turkey and some east Aegean islands. The three species P. pulcher, P. lodosi and P. sanctipauli are morphologically and bioacoustically quite similar. P. sanctipauli and P. pulcher are distinct species, P. lodosi, however, possesses a combination of the key characters of the other two species. It may be a relict species or, in our opinion more probably, a species of hybrid origin.
The taxonomy of European Eristalinus syrphid flies is reviewed. New data on their life histories, biological notes and a key to species using pupal characters are provided. The larvae and puparia of Eristalinus taeniops (Wiedemann, 1818) and Eristalinus megacephalus (Rossi, 1794) are described for the first time, including new morphological characters of the thoracic respiratory process of all species. The morphology of the male genitalia of E. megacephalus is described and compared with that of E. taeniops.
The results of our morphological studies of the male genitalia and molecular data (mitochondrial COI and nuclear 28S rDNA) do not support the traditional adult classification based on the patterning on the eyes (fasciate vs punctate). We present a phylogeny of the species based on molecular data. The molecular and morphological data indicate that the relationship between some species with punctate eyes and those with fasciate eyes may be closer than with other species with punctate eyes. Moreover the results of the molecular studies support two clades, which does not accord with the traditional arrangement of this group of Syrphidae.
Accordingly we propose that the characters of male genitalia stated by Kanervo in 1938 (but subsequently largely ignored) for arranging the European species of the Eristalinus-Eristalodes-Lathyrophthalmus complex, are suitable for classifying these species.