Small subunit rRNA sequences were obtained from 38 representatives mainly of the nematode orders Spirurida (Camallanidae, Cystidicolidae, Daniconematidae, Philometridae, Physalopteridae, Rhabdochonidae, Skrjabillanidae) and, in part, Ascaridida (Anisakidae, Cucullanidae, Quimperiidae). The examined nematodes are predominantly parasites of fishes. Their analyses provided well-supported trees allowing the study of phylogenetic relationships among some spirurine nematodes. The present results support the placement of Cucullanidae at the base of the suborder Spirurina and, based on the position of the genus Philonema (subfamily Philoneminae) forming a sister group to Skrjabillanidae (thus Philoneminae should be elevated to Philonemidae), the paraphyly of the Philometridae. Comparison of a large number of sequences of representatives of the latter family supports the paraphyly of the genera Philometra, Philometroides and Dentiphilometra. The validity of the newly included genera Afrophilometra and Caranginema is not supported. These results indicate geographical isolation has not been the cause of speciation in this parasite group and no coevolution with fish hosts is apparent. On the contrary, the group of South-American species of Alinema, Nilonema and Rumai is placed in an independent branch, thus markedly separated from other family members. Molecular data indicate that the skrjabillanid subfamily Esocineminae (represented by Esocinema bohemicum) should be either elevated to the rank of an independent family or Daniconematidae (Mexiconema africanum) should be decreased to Daniconematinae and transferred to the family Skrjabillanidae. Camallanid genera Camallanus and Procamallanus, as well as the subgenera Procamallanus and Spirocamallanus are confirmed to be paraphyletic. Paraphyly has also been found within Filarioidea, Habronematoidea and Thelazioidea and in Cystidicolidae, Physalopteridae and Thelaziidae. The results of the analyses also show that Neoascarophis, Spinitectus and Rhabdochona are monophyletic, in contrast to the paraphyletic genus Ascarophis. They further confirm the independence of two subgenera, Rhabdochona and Globochona, in the genus Rhabdochona. The necessity of further studies of fish-parasitizing representatives of additional nematode families not yet studied by molecular methods, such as Guyanemidae, Lucionematidae or Tetanonematidae, is underscored.
The genus Dasytricheta Bernhauer, 1943 is redefined. The genus Pyromecroma Cameron, 1945 is considered a new synonym of Dasytricheta. Eleven valid species are recognised in the genus: Dasytricheta spectabilis Bernhauer, 1943 (the type species of Dasytricheta), D. funesta (Broun, 1912) comb. n. (the type species of Pyromecroma, originally described in Myrmecopora Saulcy, 1864), and nine species described as new: Dasytricheta haastiana sp. n., D. hookeriana sp. n., D. intermedia sp. n., D. kapuniana sp. n., D. mahitahiana sp. n., D. periana sp. n., D. shotoveriana sp. n., D. testacea sp. n. and D. waihoana sp. n. The taxa are diagnosed, keyed and illustrated. The phylogeny of Dasytricheta is analysed using cladistic methods. The systematic position of Dasytricheta within the Aleocharinae is discussed.
The phylogenetic relationships in the myrmicine ant genus Myrmecina were analyzed using 1,281 bp of the mitochondrial cytochrome c oxidase I gene. Intermorphic queens observed in M. graminicola (Europe), M. nipponica (Japan), M. americana (North America; reported for the first time) and M. sp. A (Java) were reconstructed as an ancestral trait in this genus. Molecular-clock-based age estimates suggest that queen polymorphism evolved in Myrmecina at the latest during the Miocene. In terms of biogeographical regions, the inferred chronological order of divergence is: (oriental, (nearctic, (western palearctic, eastern palearctic))).
The box tree moth, Cydalima perspectalis (Walker, 1859) comb. n., is native to India, China, Korea, Japan and the Russian Far East. Its larvae are a serious pest of different species of Buxus. Recently, C. perspectalis was introduced into Europe and first recorded from Germany in 2006. This species has been placed in various spilomeline genera including Palpita Hübner, 1808, Diaphania Hübner, 1818, Glyphodes Guenée, 1854 and the monotypic Neoglyphodes Streltzov, 2008. In order to solve this nomenclatural confusion and to find a reasonable and verifiable generic placement for the box tree moth, the morphology of the above mentioned and some additional spilomeline taxa was investigated and their phylogeny analysed. The results show that C. perspectalis belongs to a monophylum that includes three of the genera in which it was previously placed: Glyphodes, Diaphania and Palpita. Within this monophylum, it is closely related to the Asian Cydalima Lederer, 1863. As a result of this analysis, Sisyrophora Lederer, 1863 syn. rev. and Neoglyphodes Streltzov, 2008 syn. n. are synonymised with Cydalima Lederer, 1863, and five species are transferred to this genus: Cydalima capriniodes (Hampson, 1912) (Glyphodes) comb. n., Cydalima decipiens (Hampson, 1912) (Glyphodes) comb. n., Cydalima joiceyi (Janse, 1924) (Margaronia) comb. n., Cydalima perspectalis (Walker, 1859) (Phakellura) comb. n. and Cydalima pfeifferae (Lederer, 1863) (Sisyrophora) comb. rev.
A new genus and new species of Cantacaderinae (Heteroptera: Tingidae) is described, Caledoderus monteithi. A key to genera is provided. The phylogenetic relationships among the Cantacaderinae, including this new genus and species, are revisited. The results are congruent with previous studies. However, the Ceratocaderini is a sister group of Carldrakeaninae and not Cantacaderini, even if only weakly supported by the analysis. Therefore, the status of Ceratocaderini and Cantacaderini is maintained, whereas Carldrakeanini stat. nov. is reduced to tribal level and they are all included in the Cantacaderinae., Eric Guilbert., and Obsahuje seznam literatury
Phylogenetic relationships of 27 species within the genus Ochotona were reconstructed through mitochondrial cytochrome b gene. Maximum parsimony, neighbor-joining and maximum likelihood analysis strongly indicated five major species groups: the northern group, the surrounding Qinghai-Tibet Plateau group, the Qinghai-Tibet Plateau group, the Huanghe group, and the Central Asia group. The northern group is composed of O. alpina, O. hyperborea, O. pallasi, O. princeps, and . The surrounding Qinghai-Tibet Plateau group includes O. macrotis, O. roylei, O. ladacensis, O. rutila, O. erythrotis, O. gloveri, O. brookei, O. muliensis, O. iliensis, O. himalayana, O. koslowi, O. forresti, and O. rufescens. The Qinghai-Tibet Plateau group contains O. curzoniae, O. thibetana, O. cansus, O. annectens, O. nubrica, O. daurica, and O. thomasi. The Huanghe group and the Central Asia group comprise only one species, O. huangensis and O. pusilla, respectively. Our data did not support the previous subgeneric classification. The phylogenetic trees suggested that divergences of the five groups occurred in the Early Pleistocene (about 2.8 Myr ago), and that the differentiation of the surrounding Qinghai-Tibet Plateau group, the Qinghai-Tibet Plateau group, and the Huanghe group was closely related to the uplifting of the Qinghai-Tibet Plateau and the radiation prompted by environmental changes could play a major role in these groups. Due to the relatively stable environments, however, differentiations were not so strong within the northern group and the Central Asia group, which had never invaded the Qinghai-Tibet Plateau.
1_External morphological characters were used to reconstruct a phylogeny of the mite family Syringophilidae (Acariformes: Cheyletoidea), which are permanent parasites inhabiting the quills of bird feathers. A total of 53 syringophilid genera and 79 characters were included in the data matrix; maximum parsimony (MP) and Bayesian analyses (BA) were performed to determine their phylogenetic relationships. The consensus of unweighted MP trees was weakly resolved. Only four generic groups were recognized: Aulonastus + Krantziaulonastus (i) and (Creagonycha + Kethleyana) + (Megasyringophilus + Selenonycha) (ii) – both with low Bremer support (BS 1); the subfamily Picobiinae – Picobia, Calamincola, Columbiphilus (Neopicobia + Rafapicobia) (BS 12) (iii) and Psittaciphilus generic group – (Meitingsunes + Psittaciphilus) (Peristerophila + (Neoperisterophila + (Castosyringophilus + Terratosyringophilus))) (BS 2) (iv). BA revealed a consensus tree with a topology similar to MP. The two main groups recognized by MP, the subfamily Picobiinae and Psittaciphilus, both received the highest support of 1; while two other groups recognized by MP – Aulonastus + Krantziaulonastus and (Creagonycha + Kethleyana) + (Megasyringophilus + Selenonycha) received relatively low support of 0.73–74 and 0.76–77, respectively., 2_The consensus of re-weighted MP trees was almost fully resolved but, the majority of the generic groups, excluding the Picobiinae and Psittaciphilus were supported by just a few non-unique synapomorphies with a high probability of homoplastic origin. The most intriguing result is the paraphyly of the Syringophilinae in respect to picobiines. The pattern of the re-weighted tree demonstrates only patches of parallel evolution at the level of syringophilid genera and bird orders. Perhaps horizontal shifts on phylogenetically distant hosts and colonization of quill (calamus) types other than primaries and secondaries were also important in the evolution of the syringophilids., Maciej Skoracki, Eliza Glowska, Andre V. Bochkov., and Obsahuje seznam literatury
The phylogenetic relationships of the three major species groups of Tribolium (Coleoptera: Tenebrionidae) were inferred using the simultaneous analysis of 642 bp of the most conserved part of mitochondrial DNA (mt DNA) cytochrome oxidase I (COI) and 448-452 bp of mt 16S rDNA. High sequence divergence was observed for both genes even among sibling species. The analysis of the combined segments of COI and 16S rDNA sequences produced a phylogenetic tree with moderate level of confidence. The tree topology showed monophyly of the genus Tribolium whose species were separated into three groups: "brevicornis" group (with T. brevicornis as the only representative), "castaneum" group (with T. castaneum, T. freemani, T. madens and T. audax) and "confusum" group (with T. confusum, T. anaphe and T. destructor). Sibling species pairs T. castaneum - T. freemani and T. madens - T. audax are clearly resolved. The preliminary results presented here give moderate support to the previously proposed phylogeny based on morphological data.
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.