Members of the clade Trichophora (Hemiptera: Heteroptera: Pentatomomorpha) have trichobothria on their abdominal sterna. There is no comparative study of the fine structure of abdominal trichobothria in the group and until now the trichobothria of their immatures were virtually unknown. The fine structure of the abdominal trichobothrial complex (= the trichobothrium and its associated structures) of adults of 98 species belonging to 25 families in 5 superfamilies and larvae of 7 species belonging to 7 families in 2 superfamilies of Trichophora were examined using scanning electron microscopy. This study indicates that the fine structure of the abdominal trichobothria is very variable and useful for determining evolutionary lineages within the clade. Six types of bothria, three of trichomes and three of microtrichia are recognized and their evolutionary transformations discussed. Changes in the size of trichomes, and density and size of the microtrichia during the postembryonic development of selected species are discussed.
A new species of Acanthochondria Oakley, 1927 (Copepoda, Poecilostomatoida, Chondracanthidae), parasitic on Serranus auriga (Cuvier) from the Argentinean coastal zone, is described and illustrated. The new species differs from its congeners by the relative length of the neck and the protopod of leg 2. This is the second record of this genus for the South-eastern Atlantic and the first one from a serranid host.
Based on the study of type material, two new genera of cestodes (Cyclophyllidea: Anoplocephalidae) are proposed for Paranoplocephala Lühe, 1910 sensu lato species from African rodents. Afrojoyeuxia gen. n., proposed for A. gundii (Joyeux, 1923) comb. n. from Ctenodactylus gundi (Rothmann) (Hystricomorpha: Ctenodactylidae), is characterized by a high length/width ratio of mature proglottids, longitudinally extensive testicular field positioned anterior to the female glands, an ovoid or subspherical cirrus-sac and a thick, conical cirrus. Hunkeleriella gen. n., proposed for H. dasymidis (Hunkeler, 1972) comb. n. from Dasymys incomtus (Sundevall) (Myomorpha: Muridae), differs from related genera mainly by its short (10-20 mm) and wide strobila and neck, unilateral genital pores (exceptionally with a few changes per strobila), the position of the genital pores (slightly anterior to the middle of proglottid margin) and initially tube-like early uterus (later reticulated). Parandrya Gulyaev et Chechulin, 1996, earlier suggested to be a junior synonym of Paranoplocephala, is considered to be a valid, independent genus. Evidence of non-monophyly and need for a taxonomic revision of Paranoplocephala sensu lato, as well as the phylogenetic position of A. gundii and H. dasymidis are discussed.
Over the last two decades my colleagues and I have assembled the literature on a good percentage of most of the coccidians (Conoidasida) known, to date, to parasitise: Amphibia, four major lineages of Reptilia (Amphisbaenia, Chelonia, Crocodylia, Serpentes), and seven major orders in the Mammalia (Carnivora, Chiroptera, Lagomorpha, Insectivora, Marsupialia, Primates, Scandentia). These vertebrates, combined, comprise about 15,225 species; only about 899 (5.8%) of them have been surveyed for coccidia and 1,946 apicomplexan valid species names or other forms are recorded in the literature. Based on these compilations and other factors, I extrapolated that there yet may be an additional 31,381 new apicomplexans still to be discovered in just these 12 vertebrate groups. Extending the concept to all of the other extant vertebrates on Earth; i.e. lizards (6,300 spp.), rodents plus 12 minor orders of mammals (3,180 spp.), birds (10,000 spp.), and fishes (33,000 spp.) and, conservatively assuming only two unique apicomplexan species per each vertebrate host species, I extrapolate and extend my prediction that we may eventually find 135,000 new apicomplexans that still need discovery and to be described in and from those vertebrates that have not yet been examined for them! Even doubling that number is a significant underestimation in my opinion.
The frequencies of two hereditary coat colour types were determined in a sample of weasels, Mustela nivalis (n=1280) from the Czech and Slovak Republics. White pelage was found in four (0.49%) individuals collected in the period between October and April (n=824). All the other individuals studied had type II vulgaris coloration, characterised by an irregular border between the upper brown part of the body and the white underbelly. Distal white coloration on the feet and upper lip appeared to be unreliable in distinguishing between the two basic types of weasel summer coat. The karyotypes of five weasels from different parts of the Czech Republic contained large heterochromatic arms in six pairs of autosomes. The absence of a large heterochromatic arm in autosomal pair No. 7 differentiates the chromosomal complement of the central European weasels from those occurring in the northern parts of their range. The same karyotype found in Czech weasels was also found in an individual from European Turkey. Comparison of the available data on coat colour and chromosomal variation confirmes the existence of three major phylogenetic lineages of weasels in Europe.
Achtheres percarum von Nordmann, 1832 and Achtheres sandrae Gadd, 1901 (Lernaeopodidae) are common parasitic copepods infecting fishes in Eurasia. The former is specific to perch, Perca fluviatilis L., while the latter, to zander, Sander lucioperca (L.). Until recently these copepods have been regarded a single species. The present study was intended to analyse details of male morphology and provide their complete descriptions with differential diagnosis. Males of A. percarum and A. sandrae were collected from perch and zander at Lake Dąbie (north-western Poland). The males of A. sandrae are larger than those of A. percarum. They also differ in proportions of the first antenna, mandibular denticulation, structure of the first maxilla, and the armament of caudal ramus. The reported differences in male morphology constitute a conclusive confirmation of the separate identity of the two species.
Here we present the first evidence of female dimorphism in ectoparasitic quill mites of the family Syringophilidae (Actinotrichida: Prostigmata: Cheyletoidea). Stibarokris phoeniconaias Skoracki et OConnor, 2010 and Ciconichenophilus phoeniconaias Skoracki et OConnor, 2010 so far have been treated as two distinct species cohabiting inside the quills of feathers of the lesser flamingo Phoeniconaias minor (Geoffroy Saint-Hilaire) and the American flamingo Phoenicopterus ruber Linnaeus. Although females of these species differ morphologically by the extent of body sclerotisation, presence/absence of lateral hypostomal teeth, and shape of dorsal setae, their important common features are the lack of leg setae vs II, and both stylophore and peritremes shape. Here, we apply the DNA barcode markers to test whether the differences between S. phoeniconaias and C. phoeniconaias have a genetic basis, indicating that they really are distinct taxa, or whether they just represent two morphs of a single species. All analysed sequences (616 bp for COI and 1 159 bp for 28S rDNA) obtained for specimens representing females of both studied taxa as well as male, tritonymph, protonymph and larva of S. phoeniconaias were identical, which indicates that S. phoeniconaias and C. phoeniconaias are conspecific. The formal taxonomic consequence of our results is denial of the genus status of Ciconichenophilus Skoracki et OConnor, 2010 and species status of C. phoeniconaias, and recommendation that they should be treated as junior synonyms of Stibarokris Kethley, 1970 and S. phoeniconaias, respectively.
Torotrogla merulae Skoracki, Dabert et Ehrnsberger, 2000 and T. rubeculi Skoracki, 2004 have been considered as distinct steno- and monoxenous quill mite species (Acari: Prostigmata: Syringophilidae) parasitizing the thrushes of the genus Turdus Linnaeus and the European robin Erithacus rubecula (Linnaeus), respectively. Morphological and molecular studies on the taxonomical status of these two species provided contradictory results. Well defined differences in morphology were not supported by substantial genetic distance in nucleotide sequences of the DNA barcode (mitochondrial cytochrome c oxidase subunit I, COI, and D2 domain of the nuclear 28S rRNA gene), by the topology of the phylogenetic trees (neighbor-joining, maximum parsimony, maximum likelihood) and the network analyses of the COI haplotype genealogy (median-joining, statistical parsimony) that reveal rubeculi populations nested within merulae haplotypes. Since detected differences between T. merulae and T. rubeculi populations (1.6-2.4% for COI and 0.1% for D2) are comparable to the intraspecific level observed in majority of currently recognized European Torotrogla species and are much lower than the interspecific distances observed in the genus, we postulate their conspecificity. Because main morphological distinctions concern the structures used for feeding, we hypothesize that they are the result of phenotypic plasticity evoked by specific and different environmental conditions prevailing on the host bodies (thickness of the feather quill wall).
A new genus of Myobiidae, Hylomysobia gen. n. with two new species, H. mikhailzaitzevi sp. n. (type species) and H. chinensis sp. n., is described from gymnures of the genus Hylomys Müller (Eulipotyphla: Erinaceidae). The two species parasitize Hylomys suillus Müller from Cambodia and Vietnam, and Hylomys sinensis (Trouessart) from China, respectively. These species represent the first records of myobiid mites from species in the family Erinaceidae. The new genus differs from the closely related Eutalpacarus Jameson, 1949 by the following features: in both sexes, coxae I have a triangular process, setae ve are about three times wider than sce and c2, and coxae II bear two pairs of setae; in females, setae sci are lanceolate, setae ag1 and ag3 are absent, and the vulvar lobes are weakly developed; in males, setae e2 are absent, and setae c1, d1, d2 and e1 are situated on the genital shield. The life cycle of Hylomysobia spp. includes egg, larva, protonymph, deutonymph, and adults, male and female. In contrast to the most other myobiid genera possessing the tritonymphal stage, the deutonymphs of Hylomysobia moult directly to adults, and the tritonymphs are absent. Based on the restricted distribution of Hylomysobia species on hosts of this family (only on species of the genus Hylomys) and close morphological similarities to myobiids from Soricidae and Talpidae, it is suggested that the ancestor of this genus secondarily colonized the ancestor of Hylomys from moles or shrews.
The Microsporidia are a group of obligate intracellular parasites, now thought to be derived fungi. Presented here is a comparative small subunit rDNA (ssrDNA) analysis of 125 species of Microsporidia (sequences obtained from GenBank). This analysis shows that groups or clades are formed based largely on habitat and host. This result is supported by comparative molecular analyses of the past decade, and indicates that structural and ultrastructural characters are unreliable for distinguishing among higher-level microsporidian taxa. Our findings indicate the presence of five major clades of Microsporidia which group according to habitat. We present three new classes of Microsporidia based on natural phylogenetic groupings as illustrated by the ssrDNA analysis: Aquasporidia, Marinosporidia and Terresporidia. The names of the proposed classes reflect the habitat of each group. The class Aquasporidia, found primarily in freshwater habitats, is a paraphyletic group consisting of three clades. The Marinosporidia are found in hosts of marine origin and the Terresporidia are primarily from terrestrial environments.