The Afrotropical subgenus Disneyempis Smith of the genus Empis L. is redescribed and redefined on the basis of three synapomorphies, namely labrum lengthened, male eyes more or less broadly separated on frons with all ommatidia of equal size, female abdomen with bluish to purplish metallic reflections on terga 2-5. At present, the subgenus comprises six species: E. (D.) hirsutipennis Smith as type species, E. (D.) jacksoni Smith, E. (D.) argentea sp, n., E. (D.) spinifemorata sp. n., E. (D.) proboprocera sp. n. and one unnamed species E. (D.) sp. 1. All species are described [except E. (D.) sp. 1] and keyed. The subgenus has a tropical African geographical range including Cameroon, Democratic Republic of Congo (formerly Zaire), Republic of Congo and Gabon.
The family Rhopalothylacidae (Cestoda: Trypanorhyncha) is reviewed. The type species, Rhopalothylax gymnorhynchoides Guiart, 1935, is redescribed from the type specimens and belongs within the genus Pintneriella Yamaguti, 1934, previously described only from the plerocercus. Rhopalothylax therefore becomes a junior synonym of Pintneriella. The adult of Pintneriella musculicola Yamaguti, 1934 is described for the first time, from the shark Carcharias taurus Rafinesque from Australia. Pintneriella is characterised by two bothridia, a typical heteroacanthous armature, a unique, bipartite external seminal vesicle and a uterus deviated porally, terminating at a uterine pore. It belongs within the Heteracanthoidea but is distinguishable both from the Eutetrarhynchidae and the Gilquiniidae, the two families which it most closely resembles. Cladistic analyses align Pintneriella within the clade containing the families Gilquiniidae, Gymnorhynchidae and Molicolidae rather than with the Eutetrarhynchidae. The family Rhopalothylacidae is therefore retained provisionally to accommodate Pintneriella within the Heteracanthoidea. The second genus of the Rhopalothylacidae, Clujia Guiart, 1935, is unrecognisable from its description and cannot be redescribed from its holotype. It is therefore considered a genus inquirendum.
The taxonomy and distribution of rodents in Zambia was comprehensively summarized in 1978 by W.F.H. Ansell in his excellent book Mammals of Zambia. Despite the fact that during the last three decades many new taxonomic revisions of African rodents were published and extensive new material collected, not much work has been done on Zambian rodents since the book publication. Here we summarize the current knowledge of one of the most speciose group of African rodents, the tribe Praomyini, in Zambia. We review available historical records and revise our recently collected material by sequencing the mitochondrial DNA gene of cytochrome b. The presence of eight species of Praomyini in Zambia is documented and the pattern of their geographical distribution is described and discussed. Two species, Praomys minor and Mastomys coucha, are reported for the first time from Zambia and Praomys cf. jacksoni probably represents a new undescribed species. On the other hand, the actual occurrence of Colomys goslingi, known in Zambia only from one historical record, is questionable. The results document the usefulness of the DNA barcoding approach for description of species diversity of taxonomically complicated groups with many cryptic species.
The New World genus Ataeniopsis Petrovitz, 1973 is revised. Fifteen species are recognized including three new species: Ataeniopsis carupanoi sp. n. from Venezuela, A. jaltipani sp. n. from Mexico and A. vinacoensis sp. n. from Argentina. Lectotype of A. haroldi (Steinheil, 1872) is designated, the name of type species A. notabilis Petrovitz, 1973 is reestablished, five species are given in a new combination. The taxa are diagnosed, keyed and illustrated, and biological information and distribution data summarized following the species descriptions. A hypothetical phylogenetic analysis of Ataeniopsis based on cladistic analysis is presented.
Species of Rhamnocercinae Monaco, Wood et Mizelle, 1954 are gill parasites of sciaenid fishes (Perciformes). Seven are marine species (three in the western Atlantic and four in oriental Pacific) and one is a neotropical freshwater species (Rio Doce Basin, Brazil). While the status of the subfamily may be questioned, this assemblage of species is apparently supported by several shared apomorphic and plesiomorphic characters, such as: (1) peduncular spines with anterior and posterior roots; (2) haptor laterally expanded, armed with anchors (two pairs); bars (one ventral, two dorsal); 14 hooks and haptoral accessory spines; and (3) double (nested) tubes of the male copulatory organ (MCO), directed posteriorly with the genital pore lying posterior to the MCO. The phylogenetic hypothesis for the eight known species of this clade is: (Spinomatrix penteormos (Rhamnocercoides stichospinus, Rhamnocercoides menticirrhi) Rhamnocercus oliveri (Rhamnocercus rhamnocercus (Rhamnocercus stelliferi, Rhamnocercus bairdiella, Rhamnocercus margaritae)). This hypothesis indicates that Spinomatrix penteormos represents the sister group of all remaining rhamnocercines. The resulting phylogenetic sister-group relationships support the transfer of Rhamnocercus stichospinus Seamster et Wood, 1956 to Rhamnocercoides Luque et Iannacone, 1991 as Rhamnocercoides stichospinus (Seamster et Wood, 1956) n. comb.
The New World species of Loxocera Meigen are revised including two new species, L. (Imantimyia) ignyodactyla Buck sp. n. from Costa Rica (first record of the genus from the Neotropical region) and L. (Imantimyia) ojibwayensis Buck sp. n. from Ontario, Canada. Loxocera californica Capelle is synonymized with L. collaris Loew and lectotypes are designated for L. pleuritica Loew and L. cylindrica var. obsoleta Johnson (both synonyms of L. cylindrica Say). The New World species are diagnosed and a key to species is provided. The male and female terminalia of Loxocera are described in detail for the first time, and their functional morphology is discussed. Eggs of most species are described and a key to the known eggs of Loxocera is provided. A phylogenetic framework for the Holarctic subgenera and species groups of Loxocera is developed based on morphological characters of the adult flies. The Old World subgenus Platystyla Macquart is synonymized with Loxocera s. str., and Imantimyia Frey is reinstated as a valid subgenus including all Holarctic species previously placed in Loxocera s. str. except the L. aristata species group. This leads to the following new subgeneric combinations: L. (L.) malaisei Frey comb. n., L. (L.) matsumurai Iwasa comb. n., L. (L.) monstrata Iwasa, comb. n., and L. (L.) omei Shatalkin comb. n. The species groups of Imantimyia are redefined, i.e. the L. achaeta-group (7 spp.), the L. fulviventris-group (4 spp.), and the L. albiseta-group (1 sp.). The Oriental subgenus Asiopsila Shatalkin is referred to Psila Meigen s. l. as a subgenus based on characters of the egg, resulting in fourteen new generic combinations: Psila (Asiopsila) brevibuccata (Shatalkin) comb. n., P. (A.) burmanica (Frey) comb. n., P. (A.) decorata (de Meijere) comb. n., P. (A.) derivata (Shatalkin) comb. n., P. (A.) formosana (Hennig) comb. n., P. (A.) freidbergi (Shatalkin) comb. n., P. (A.) humeralis (de Meijere) comb. n., P. (A.) kambaitensis (Frey) comb. n., P. (A.) limpida (Shatalkin) comb. n., P. (A.) maculipennis (Hendel) comb. n., P. (A.) michelseni (Shatalkin) comb. n., P. (A.) pleuralis (Frey) comb. n., P. (A.) primigena (Shatalkin) comb. n., and P. (A.) vittipleura (Shatalkin) comb. n.
Four genera of the blister beetle tribe Cerocomini are revised, including the new genus Somalarthrocera. The genera Rhampholyssa Kraatz, 1863 and Somalarthrocera comprise two species each, whereas Anisarthrocera Semenow, 1895 and Rhampholyssodes Kaszab, 1983 are monotypic. S. savanicola sp. n. from Kenya is described, S. semirufa (Fairmaire, 1882) comb. n. is proposed, as well as new synonymy: A. batesi (Marseul, 1872) = A. batesi villiersi Kaszab, 1968. Phylogenetic relationships among the six genera of the tribe are defined by a cladistic analysis, which indicates three clades, one basal, represented by the genus Cerocoma Geoffroy, 1762, the second including Anisarthrocera and the pair Rhampholyssa and Rhampholyssodes, and the third including Diaphorocera Heyden, 1863 and Somalarthrocera. Bionomical information available for the four revised genera is summarised. Keys to these genera and to the species of the two non-monotypic genera are presented, as well as diagnoses of genera and species and catalogue of localities. Anisarthrocera is distributed in the northern Persian Gulf, Rhampholyssa in the Turanian depression, Rhampholyssodes is endemic to the eastern Arabian Peninsula, and Somalarthrocera is distributed in Somalia and Kenya. A brief biogeographical analysis of this primarily Palaearctic tribe is also presented.
The subgenus Gnypetalia Cameron, 1939 is redefined and raised to the genus rank. Eleven valid species are recognised in the genus, six of which are described as new: Gnypetalia armata sp. n. (Solomon Islands), G. cuccodoroi sp. n. (Philippines: Luzon), G. insularis sp. n. (Solomon Islands), G. luzonica sp. n. (Philippines: Luzon, Palawan), G. nitida sp. n. (Indonesia: Sulawesi) and G. penrisseni sp. n. (Malaysia: Sarawak). One new synonym is established: Gnypetalia parva Cameron, 1950 = Ischnopoda (Caliusa) finitima Pace, 1998 syn. n. Five species are given in new combination: Gnypetalia indica (Cameron, 1939) comb. n (= Gnypeta (Gnypetalia) indica), Gnypetalia parva (Cameron, 1950) comb. n. [= Gnypeta (Gnypetalia) parva], Gnypetalia rougemontiana (Pace, 1986) comb. n [= Tachyusa (Caliusa) rougemontiana], Gnypetalia song (Pace, 1990) comb. n. [= Tachyusa (Caliusa) song] and Gnypetalia thoracica (Fauvel, 1879) comb. n. (= Tachyusa thoracica). Lectotype is designated for Gnypeta indica Cameron, 1939. The taxa are diagnosed, keyed and illustrated. The phylogeny of the aleocharine genus Gnypetalia is analysed using cladistic methods. The monophyly of Gnypetalia is confirmed and three major monophyletic species group are recognised.
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 Neochauliodes sundaicus species-group is newly proposed, containing six species and endemic to Indo-Malaysia. All six species are described and illustrated, including two new species: Neochauliodes parvus Liu, Hayashi & Flint, sp. n. and N. peninsularis Liu, Hayashi & Flint, sp. n. Full species status is given to N. maculatus Stitz, 1914, stat. n. and N. borneensis van der Weele, 1909, stat. n. A cladistic analysis is conducted to reconstruct the species level phylogeny of the N. sundaicus group based on the morphological data. Combining the present morphological phylogeny and historical geography of Indo-Malaysia, the origin and speciation of this species-group is briefly discussed.