Long-eared bats of the genus Plecotus are widespread over most of temperate Eurasia, marginally reaching the African continent and Macaronesia. Previously, all African populations were assigned to one species, P. auritus, and later to P. austriacus. We analysed museum specimens of African long-eared bat populations using both morphologic and genetic techniques. Based on morphological evidence we recognise four well-defined allopatric populations in northern Africa. They differ in fur coloration, skull morphology and bacular traits. The molecular data support a division of the African populations into at least three well-separated evolutionary lineages. With a combination of these data we define three species of Plecotus occurring in Africa (incl. the Canary Islands) and describe a new subspecies. Small, very pale greyish-brown Egyptian long-eared bats (P. christii Gray, 1838) inhabit desert and semi-deserts habitats of eastern Sahara (Libyan Desert, Nile Valley of Egypt and northern Sudan). Smaller to medium-sized, dark brown Ethiopian long-eared bats (P. balensis Kruskop et Lavrenchenko, 2000) inhabit the Ethiopian Highlands above 2000 metres a. s. l. This form represents the only Afro-tropical species of Plecotus. Large, dark greyish Canarian long-eared bats (P. teneriffae teneriffae Barret-Hamilton, 1907) occur on the three western islands of the Canarian Archipelago. A medium-sized greyish-brown Gaisler’s long-eared bat, P. teneriffae gaisleri subsp. n., is described from the Mediterranean region of Cyrenaica, north-eastern Libya. Due to the lack of substantial morphological differences we preliminarily consider the Maghrebian population of long-eared bats to be consubspecific with P. teneriffae gaisleri subsp. n. The systematic position of the population of Cape Verde Islands remains uncertain.
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.
A survey of proteocephalidean cestodes found in the firewood catfish Sorubimichthys planiceps (Spix et Agassiz) from the Amazon River is provided. The following taxa parasitic in S. planiceps are redescribed on the basis of their type specimens and material collected recently in the Amazon River, near the type localities in Brazil, and in Iquitos, Peru: Monticellia lenha Woodland, 1933; Nomimoscolex lenha (Woodland, 1933) (syn. Proteocephalus lenha Woodland, 1933); and Monticellia megacephala Woodland, 1934, for which a new genus, Lenhataenia, is proposed, with L. megacephala (Woodland, 1934) comb. n. as its type and only species. The new genus is a member of the Monticelliinae, i.e. has all genital organs in the cortex, and is most similar to Chambriella in possessing biloculate suckers and lacking a metascolex. It differs in the morphology of the cirrus-sac that contains a strongly coiled, thick-walled internal sperm duct (vas deferens) and a muscular cirrus of the appearance typical of most proteocephalideans, whereas that of Chambriella is sigmoid, with voluminous, tightly sinuous thick-walled internal sperm duct. In addition, Lenhataenia possesses a well developed internal musculature, whereas the internal musculature of Chambriella is weakly developed, formed by a low number of muscle fibres. The scolex morphology and distribution of microtriches of Peltidocotyle lenha (Woodland, 1933) (syn. Othinoscolex lenha Woodland, 1933 and Othinoscolex myzofer Woodland, 1933), Chambriella sp. and Choanoscolex sp. are described using scanning electron microscopy. The two latter taxa may be new for science and are reported from S. planiceps for the first time .
Males of the nematode Philometra lateolabracis (Yamaguti, 1935), the type species of the genus Philometra Costa, 1845, were discovered for the first time in gonads of its type host, the Japanese seaperch, Lateolabrax japonicus (Cuvier). Morphological comparisons carried out between the collected male and female P. lateolabracis with the male and female philometrid nematodes previously reported as P. lateolabracis infecting chicken grunt, Parapristipoma trilineatum (Thunberg), and red sea bream, Pagrus major (Temminck et Schlegel), revealed that the latter represent two new species, Philometra isaki sp. n. and Philometra madai sp. n., respectively. Molecular comparison of ITS2 rDNA between P. lateolabracis and P. madai supported the morphological conclusion that the two nematodes obtained from different fish species should be assigned to different species.
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.
The intra- and interspecific variability in the West Palaearctic tibialis-group species of the subgenus Pandasyopthalmus (Diptera: Syrphidae: Paragus) was analysed. Novel immature and molecular characters were studied and the traditionally used adult characters reviewed with the aim of establishing the status of the most widespread taxa of the tibialis-group in the Palaearctic region. Moreover, a review of the morphology of the larvae of the subgenus Pandasyopthalmus is also presented and includes the first description of the chaetotaxy of the larval head of Syrphidae. The larval morphology showed a continuum between two extremes. There is intraspecific variability in the male genitalia characters typically used for diagnostic species identification in this group. Molecular characters of the mitochondrial cytochrome c-oxidase subunit I (COI) was invariant for the West Palaearctic Pandasyopthalmus taxa analysed. Despite the fact that no great differences were found when compared with Afrotropical tibialis-group individuals (uncorrected pairwise divergence 0.17-0.35%), the divergences of the West Palaearctic vs. Nearctic and Austral-Oriental tibialis-group taxa varied between 1.15-2.75% (uncorrected pairwise divergence). Molecular characters of the nuclear ribosomal internal transcribed spacer region (ITS2) revealed several molecular haplotypes of a dinucleotide repeat that was not constrained to morphospecies or to populations of the same geographic origin. The closely related and morphologically similar species of the tibialis-group known from the West Palaearctic region are separable in most cases only by the shape and size of male postgonites. The results of this study support the presence of a single polymorphic taxon in the West Palaearctic region (or a very recent origin of the taxa studied). Moreover larval morphology and the lack of a clear relation between ITS2 haplotypes and the geographic distribution or adult morphology, support the taxonomic implications of barcode taxonomy based on mitochondrial DNA for this species-group of Syrphidae.
The Capsalidae are monogeneans parasitizing ''skin'', fins and gills of marine fishes. Some capsalids are pathogenic to cultivated fish and a few have caused epizootic events. It is a cosmopolitan family with broad host associations (elasmobranchs and teleosts, including sturgeons). Approximately 200 capsalid species are placed in nine subfamilies and 44-46 genera, some of which are well known (Benedenia, Capsala, Entobdella, Neobenedenia). Sturgeons host two capsalid species (Nitzschiinae) and 15 species in five genera are reliably reported from elasmobranchs. The combination of ancient (shark, ray, sturgeon) and modern (teleost) host fish lineages indicates that capsalid evolution is likely a blend of coevolution and host-switching, but a family phylogeny has been lacking due to deficient knowledge about homologies. The current phenetic subfamilial classification is discussed in detail using a preliminary phylogeny generated from large subunit ribosomal DNA sequence data from representatives of five subfamilies. Monophyly of the Capsalidae is supported by possession of accessory sclerites. Hypotheses are proposed for the possible radiation of capsalids. A suggestion that Neobenedenia melleni, a pathogenic species atypical due to its broad host-specificity (>100 host teleost species from >30 families in five orders), may be a complex of species is supported from genetic evidence. This may explain peculiarities in biology, taxonomy, host associations and geographic distribution of N. 'melleni' and has implications for fish health. Holistic studies using live and preserved larval and adult capsalid specimens and material for genetic analysis are emphasised to further determine identity, phylogeny and details of biology, especially for pathogenic species.
Adults of two coniopterygid species, Aleuropteryx juniperi Ohm, 1968 (Aleuropteryginae) and Semidalis aleyrodiformis (Stephens, 1836) (Coniopteryginae), were studied using scanning electron microscopy. Interspecific differences in the ultrastructure of the integument of all the major parts of the body were identified and described, and the functional and phylogenetic implications of the differences discussed. Additionally, the enlarged terminal segment of the labial palps of the Coniopterygidae and the Sisyridae, which up to now has been used as an argument for a sister-group relationship between these two families, was subjected to a thorough comparison. The very different morphology makes independent enlargement of the terminal palpal segment in both families plausible. This finding is congruent with the earlier hypothesis of a sister-group relationship between Coniopterygidae and the dilarid clade, which was proposed on the basis of molecular data, larval morphology and male genital sclerites. Finally, a new classification of the coniopterygid subfamilies is presented based on characters of the larval head (prominence of the ocular region, relative length of sucking stylets). The following relationship is hypothesized: (Brucheiserinae + Coniopteryginae) + Aleuropteryginae, and the implications of this hypothesis for the phylogenetic interpretation of the ultrastructural differences that we found are discussed: (1) The wax glands, as well as plicatures, are interpreted as belonging to the ground pattern of the family Coniopterygidae, and (2) the wax glands are considered to have been reduced in Brucheiserinae and the plicatures in Coniopteryginae. A distinct (though reduced) spiraculum 8 was detected in Semidalis aleyrodiformis; as a consequence the hypothesis that the loss of spiraculum 8 is an autapomorphy of Coniopteryginae is refuted.
The type species of Pseudopsila Johnson, P. fallax (Loew), and two related species are found to belong in Psila s. str., and Pseudopsila is thus synonymized with Psila Meigen. The remaining species formerly included in Pseudopsila form a monophyletic group here described as Xenopsila Buck subgen. n. [i.e., Psila (Xenopsila) collaris Loew comb. n., P. (X.) bivittata Loew comb. n., P. (X.) lateralis Loew comb. n., P. (X.) arbustorum Shatalkin comb. n., P. (X.) nemoralis Shatalkin comb. n., P. (X.) tetrachaeta (Shatalkin) comb. n., P. (X.) maculipennis (Frey) comb. n., P. (X.) nigricollis (Frey) comb. n., P. (X.) nigrohumera (Wang & Yang) comb. n.]. A key to the Nearctic species of Xenopsila and the Psila fallax-group is provided. The placement of Xenopsila in Psila s. l. is confirmed by newly recognised synapomorphies of the egg stage. The somewhat questionable monophyly of Psila s. l. is confirmed based on these new synapomorphies, thereby slightly expanding its taxonomic limits to also include Asiopsila Shatalkin. The morphology of the male genitalia of Xenopsila is discussed in detail, clarifying confused homologies and character polarities in the hypandrial complex. Evolutionary trends in the development of the hypandrium in the subfamily Psilinae are discussed.
Specimens of Neoechinorhynchus (Neoechinorhynchus) poonchensis sp. n. are described from Schizothorax richardsonii (Gray) in the Poonch River, Jammu and Kashmir. Specimens are thick-walled with dissimilar dorsal and ventral para-receptacle structures, anteriorly manubriated hooks, two giant nuclei in each lemniscus and many subcutaneousy. The lemnisci barely overlap the larger anterior testis, the cement gland has eight giant nuclei, and the seminal vesicle is large with thin walls. The vagina is unremarkable but the long uterus is made up of four specialised regions. Neoechinorhynchus rigidus (Van Cleave, 1928), resembles N. poonchensis sp. n. It is distinguished from N. poonchensis sp. n. by having smaller trunk, proboscis, and male reproductive structures, equal testes, unequal lemnisci with three giant nuclei each, and much larger anterior proboscis hook (130 μm in males) than that originally described by Van Cleave (1928) (70 μm in a female). Anterior hook length alone is sufficient to conclude that the N. rigidus of Datta (1937) is not the same species as the N. rigidus of Van Cleave (1928). Van Cleave's (1928) species remains valid and that of Datta (1937) is considered a different species named Neoechinorhynchus pseudorigidus sp. n., herein. Micropores of N. poonchensis sp. n. have variable distribution in different trunk regions and the Energy Dispersive X-ray analysis demonstrated higher levels of sulfur and lower levels of calcium and phosphorus. Sequences of the 18S rDNA gene from nuclear DNA, and cytochrome c oxidase subunit I (cox1) from mitochondrial DNA of N. poonchensis sp. n. were amplified and aligned with other sequences available on GenBank. Maximum likelihood (ML) and Bayesian inference (BI) analyses inferred for 18S rDNA and cox1 showed that N. poonchensis sp. n. was nested in a separate clade.