A new diminutive genus and species of catfish from Lake Tanganyika (Siluriformes: Clariidae)

The examination of material representing one of Lake Tanganyika's six previously recognized endemic catfish lineages, has revealed the presence of an additional genus of clariid, described here as Pseudotanganikallabes new genus. This genus is represented by a single species, Pseudotanganikallabes prognatha sp. nov., which is distinguished from all other clariids by its lack of an infraorbital series, the presence of multiple osseous connections between the swim bladder capsules and elements of the neurocranium, the absence of an ethmoid notch, the presence of a very large, egg‐shaped occipital fontanelle and the extension of the lower lip beyond the margin of the upper jaw. A combination of additional external and molecular characters serves to further distinguish this taxon from all currently recognized clariid species. Phylogenetic analysis of mitochondrial (cytb) and nuclear (18S‐ITS1‐5.8S‐ITS2‐28S) sequence data supports the creation of a new genus for this species, as it appears to represent an independent, monophyletic lineage within the family Clariidae.     

Insight into the phylogeny of African Clariidae (Teleostei, Siluriformes): implications for their body shape evolution, biogeography, and taxonomy

The phylogenetic relationships among Clariidae species (Teleostei, Siluriformes) were assessed using 563 nucleotides of the cytochrome b mitochondrial gene. We included 32 Clariidae species representative of seven genera in our analysis. Hetropneustes fossilis (Heteropneustidae) and Clarotes laticeps (Claroteidae) were used as outgroups. The molecular data identified two evolutionary lineages that correspond on one hand to African species and on the other hand to Asian species. Morphological and osteological evolution in Clariidae did not follow an orthogenetic series. Species with robust body, strong ossified head, and large adipose fin were not ancestral ones and eel-like species were not phylogenetically related and represent independent adaptation to life in mud. Adaptation to life in deep water occurred two times independently in lake Tanganyika (with Dinotopterus cunningtoni) and in Lake Malawi (with Bathyclarias species). Molecular dating using a molecular clock of 1% divergence per million years and a comparison with fossils records allowed an estimate of the timing of cladogenesis within the species studied. The Clariidae family originated in Asia 50 MY ago but contemporary African and Asian studied species originated from a common ancestor that was present on the Arabian plate about 15 MY ago. Systematic implications of these results are also discussed.     

Phylogenetic analysis and revision of the linyphiid spider genus Solenysa (Araneae: Linyphiidae: Erigoninae)

In this paper we carry out a taxonomic revision and phylogenetic analysis of the linyphiid spider genus Solenysa Simon, 1894. A total of 12 species is treated here, including five new species collected from China and Japan: Solenysa akihisai Tu sp. nov., Solenysa lanyuensis Tu sp. nov., Solenysa retractilis Tu sp. nov., Solenysa tianmushana Tu sp. nov. , and Solenysa yangmingshana Tu sp. nov. Solenysa circularis Gao, Zhu & Sha, 1993 is a junior synonym of Solenysa protrudens Gao, Zhu & Sha, 1993. We have assembled two different character matrices to reconstruct the phylogenetic relationships of Solenysa. In the first matrix (Matrix 1), five representative species of Solenysa were added to the morphological dataset of Miller & Hormiga to test the monophyly of the genus and its placement within Linyphiidae. The genitalic structures and somatic morphology of Solenysa were studied by means of scanning electron microscopy for the first time. To infer the species‐level phylogenetic relationships of Solenysa we produced a second matrix (Matrix 2) that includes all 12 Solenysa species and six outgroup species chosen from the results of the analysis of the first matrix. The two most parsimonious trees from the analysis of Matrix 1 support the monophyly of Solenysa and its placement within the ‘Distal Erigonines’ clade. The single most parsimonious tree resulting from the analysis of the second matrix suggests that the Solenysa clade includes four monophyletic groups, each group represented by a distinct genitalic pattern. The morphology of Solenysa, both somatic and genitalic, is highly autapomorphic. © 2011 The Linnean Society of London, Zoological Journal of the Linnean Society, 2011, 161 , 484–530.     

A revision and phylogenetic analysis of Stapeliopsis (Apocynaceae)

A survey of morphological characters is carried out for Stapeliopsis . The information obtained from this is combined with molecular data from the plastid trn L-F DNA region and ITS1 of the nuclear encoded 18S−26S rRNA cistron, to obtain a hypothesis of the evolutionary relationships among the species. It is shown that Stapeliopsis is monophyletic in a combined molecular and morphological analysis. Stapeliopsis is sister to a clade containing Huernia , Orbea and Tromotriche . The species of Stapeliopsis group into two clades. One contains S. khamiesbergensis , S. neronis and S. urniflora , and this is highly supported. The remaining species fall into an unsupported clade in which S. exasperata is sister to the others. The genera Hermanschwartzia Plowes and Neopectinaria Plowes are rejected. It is shown that a synapomorphy for Stapeliopsis is the laterally flattened inner corona-lobes, which touch the anthers only at their bases. Eight species of Stapeliopsis are recognized, with no subgeneric divisions.  © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society , 2005, 148 , 125–155.     

Systematic revision and molecular phylogeny of the land snail genus Fruticocampylaea (Gastropoda: Hygromiidae) from the Caucasus region

This paper presents a systematic revision and a molecular phylogenetic analysis of the Caucasian land snail genus Fruticocampylaea. The genus is newly delimited based on the reduction of the cavities adjoining the seminal duct in the penial papilla. Shell and genitalia of all five species (F. narzanensis, F. kobensis, F. tushetica sp. nov., F. christophori, F. daghestana) are described and figures provided. All synonyms and all locality records are listed. Maximum likelihood and Bayesian analyses of mitochondrial and nuclear DNA sequences (fragments of cox1, 16S rDNA, ITS2 and 28S rDNA) confirm the monophyly of Fruticocampylaea. The reduction of the dart apparatus and the conical plug, via which the dart apparatus inserts into the vagina, as well as the molecular phylogenetic analyses, suggests a sister group relationship between Fruticocampylaea and Circassina (without Abchasohela). Furthermore, the molecular phylogenetic analyses indicate that the Fruticocampylaea species originated in a rapid radiation. The uplift of the Greater Caucasus in the Late Miocene or Pliocene or climatic changes at the end of the Pliocene or in the early Pleistocene may have caused the radiation of Fruticocampylaea. Low intraspecific variability can be explained by population bottlenecks during Pleistocene glacial periods followed by postglacial population increase.

http://zoobank.org/urn:lsid:zoobank.org:pub:AB15158D-21A3-4945-8D49-F7DE8E406E2B     

Taxonomic revision of the genus Carasobarbus Karaman, 1971 (Actinopterygii,Cyprinidae)

Representatives of the fish genus Carasobarbus Karaman, 1971 (Actinopterygii: Cyprinidae) from the Middle East and North Africa were previously placed in 14 different genus-group taxa (Barbellion, Barbus, Barynotus, Capoeta, Carasobarbus, Cyclocheilichthys, Kosswigobarbus, Labeobarbus, Luciobarbus, Pseudotor, Puntius, Systomus, Tor and Varicorhinus). The generic assignment of several species changed frequently, necessitating a re-evaluation of their taxonomic status. In this study, the genus Carasobarbus is revised based on comparative morphological examinations of about 1300 preserved specimens from collections of several museums and freshly collected material. The species Carasobarbus apoensis, Carasobarbus canis, Carasobarbus chantrei, Carasobarbus exulatus, Carasobarbus fritschii, Carasobarbus harterti, Carasobarbus kosswigi, Carasobarbus luteus and Carasobarbus sublimus form a monophyletic group that shares the following combination of characters: medium-sized barbels with a smooth last unbranched dorsal-fin ray, nine or 10 branched dorsal-fin rays and six branched anal fin-rays; scales large, shield-shaped, with many parallel radii; the lateral line containing 25 to 39 scales; the pharyngeal teeth hooked, 2.3.5-5.3.2 or 2.3.4-4.3.2; one or two pairs of barbels. The species are described in detail, their taxonomic status is re-evaluated and an identification key is provided. A lectotype of Systomus luteus Heckel, 1843 is designated. Carasobarbus Karaman, 1971, Kosswigobarbus Karaman, 1971, and Pseudotor Karaman, 1971 are subjective synonyms, and acting as First Reviser we gave precedence to the name Carasobarbus.     

Morphology of the gas bladder in bumblebee catfishes (Siluriformes,Pseudopimelodidae)

The gross morphology of the gas bladder is described and compared for representatives of all valid genera of Pseudopimelodidae (Siluriformes). Cephalosilurus albomarginatus and species of Batrochoglanis, and Microglanis have the most basic form: a large, cordiform gas bladder with a simple internal T‐shaped septum. Cephalosilurus apurensis, C. fowleri, and C. nigricauda also have a large, cordiform gas bladder, but they have well‐developed trabeculae associated with the internal T‐shaped septum, and a pair of well‐developed constrictor muscles inserted on the external wall; the latter feature is present in most species of Pimelodidae, but absent in all other catfishes. The monotypic Lophiosilurus alexandri also has well‐developed constrictor muscles, and its gas bladder is moderately sized. The species of Pseudopimelodus and Cruciglanis have a diminutive gas bladder partially divided into two lateral sacs without internal communication, and lack constrictor muscles. The parapophysis of the fourth vertebra is a wide and long shelf connected to the dorsal surface of the gas bladder in most pseudopimelodid genera. However, in the species of Pseudopimelodus and Cruciglanis the parapophysis of the fourth vertebra is shorter and has its anterior ramus folded back, partially covering the gas bladder anteroventrally; and the tympanic opening is smaller than in species of the other genera. Five phylogenetic characters are proposed based on the morphology of the gas bladder and associated structures in species of Pseudopimelodidae, and the evolution of those characters in the family is discussed. J. Morphol., 2011. © 2011 Wiley‐Liss, Inc.     

Molecular studies resolve Nyholmiella (Orthotrichaceae) as a separate genus

Two Orthotrichum species of the subgenus Orthophyllum were compared with other representatives of this genus using internally transcribed spacer regions 1 and 2, the chloroplast trn H-psbA region, and inter-simple sequence repeat (ISSR) and intron-exon splice conjunction (ISJ) markers. The ISSR and ISJ markers used revealed many bands and mutations specific only to O. Gymnostomum and O. Obtusifolium. Phylogenetic analysis clearly supported previous concepts postulating that species of the subgenus Orthophyllum should be recognized as the separate genus Nyholmiella.     

Comparative morphology of the gas bladder in driftwood catfishes (Siluriformes: Auchenipteridae)

The gross morphology of the gas bladder is described and illustrated for representatives of most species and all valid genera of the Auchenipteridae (Siluriformes). Although, a simple cordiform gas bladder is present in some species of the family, others are characterized by their distinctive gas‐bladder shape and diverticula disposition. An acute posterior end of the gas bladder characterizes Centromochlus heckelii and C. macracanthus, and is variably present in specimens of Auchenipterus. Tocantinsia piresi and Asterophysus batrachus have distinctive gas bladders differing in number of diverticula (two or many). The two species of Trachycorystes are diagnosed based on their gas bladder morphology: T. menezesi has a simple cordiform bladder, whereas T. trachycorystes has a pair of lateral diverticulum and, usually, a well‐developed terminal diverticulum. Species of Auchenipterichthys are characterized by having a secondary bladder with simple chamber. Short or elongate and divergent terminal diverticula are exclusive to most cis‐andine species of Trachelyopterus. Tetranematichthys and trans‐andine species of Trachelyopterus share a well‐developed secondary chamber or terminal diverticula ventrally or dorsally connected to the posterior chambers. The small‐sized species of Ageneiosus have well‐developed gas bladders with a pair of posterior diverticula, whereas large‐sized species have a reduced gas bladder with tunica externa varying from non‐, partially, or completely ossified. Eight phylogenetic characters are proposed based on the morphology of the gas bladder and associated structures in species of Auchenipteridae, and the evolution of those characters in the family discussed. J. Morphol., 2012. © 2012 Wiley Periodicals, Inc.     

Molecular studies resolve Nyholmiella (Orthotrichaceae) as separated genus

Two Orthotrichum species of the subgenus Orthophyllum were compared with other representatives of this genus using the internally transcribed spacer regions 1 and 2, the chloroplast trnH-psbA region and ISSR and ISJ DNA markers. The applied DNA markers revealed many bands and mutations specific only to O. gymnostomum and O. obtusifolium. A phylogenetic analysis clearly supported the previous concepts postulating that species of the subgenus Orthophyllum should be recognized as separate genus Nyholmiella.     

Cladistic analysis and taxonomic revision of the genus Karos Goodnight & Goodnight, 1944 (Opiliones,Laniatores, Stygnopsidae)

A cladistic analysis of the genus Karos Goodnight & Goodnight, 1944, was performed using morphological data of the somatic and male genitalia characters. The analysis included 23 terminal taxa, including nine of the 11 described species of the genus plus nine new species according to the previous generic diagnosis and five species as outgroups. According to the topologies obtained by parsimony analyses, the genus is a paraphyletic assemblage, referred here as the Karos genus‐group. Therefore, the genus Karos is rediagnosed here and now includes seven species: Karos barbarikos Goodnight & Goodnight, 1944 (type), Karos parvus Goodnight & Goodnight, 1971, Karos projectus Goodnight & Goodnight, 1971, K aros hexasetosus sp. nov. , K aros monjarazi sp. nov. , K aros singularis sp. nov. , and K aros tersum sp. nov. The genera Monterella Goodnight & Goodnight, 1944, Montabunus Goodnight & Goodnight, 1945, Chapulobunus Goodnight & Goodnight, 1946, and Potosa Goodnight & Goodnight, 1947 are revalidated, rediagnosed, their respective type species are redescribed and the following species are described: Chapulobunus poblano sp. nov. and Potosa reddelli sp. nov. The genera Crettaros gen. nov. , Huasteca gen. nov. , and Mictlana gen. nov. , and the following species are described: Crettaros santibanezi sp. nov. (type), Crettaros valdezi sp. nov. , and Huasteca silhavyi sp. nov. The following new combinations are proposed: Huasteca gratiosa (Goodnight & Goodnight, 1971) comb. nov. (type), Huasteca rugosa (Goodnight & Goodnight, 1971) comb. nov. and Mictlana inops (Goodnight & Goodnight, 1971) comb. nov. (type). Karos brignolii ?ilhavý, 1974, is considered a junior synonym of Huasteca rugosa. Finally, ‘Karos’ depressus Goodnight & Goodnight, 1971 is considered incertae sedis until adult males can be studied. Diagnoses of the Karos and Paramitraceras genus‐groups, and an identification key to the eight genera and 19 species of the former are provided. © 2015 The Linnean Society of London     

A revision of the Appalachian millipede genus Brachoria Chamberlin, 1939 (Polydesmida: Xystodesmidae: Apheloriini)

The apheloriine millipede genus Brachoria as presented here comprises 34 species distributed throughout the south‐eastern US Appalachian Mountains. Members of this genus are blind (like all millipedes in the order Polydesmida), large (4–6 cm in length), and display conspicuous aposematic coloration in yellow, red, orange, and violet. Many Brachoria species participate in Müllerian mimicry rings with co‐occurring Apheloriini, in particular with species in the genus Apheloria. Some areas contain five co‐mimic species of Apheloriini and a high local density totalling 43 individuals per 50 m². Since the first revision in 1959, workers have suggested that many more species were awaiting discovery in the Cumberland Mountains. Here I present a taxonomic revision and describe ten new species: Brachoria badbranchensis , Brachoria blackmountainensis , Brachoria campcreekensis , Brachoria cumberlandmountainensis , Brachoria flammipes , Brachoria grapevinensis , Brachoria guntermountainensis , Brachoria hendrixsoni , Brachoria sheari , and Brachoria virginia . Five of these new species occur in the Cumberland Mountain Thrust Block region and five occur elsewhere throughout the Appalachian Highlands in eastern Kentucky, north‐eastern Alabama, southern West Virginia, south‐western Virginia, and the Blue Ridge Mountains of Tennessee. A molecular phylogeny of Brachoria species is well supported at deeper divergences, corresponds closely with geography, and is used as a phylogenetic basis for the taxonomy presented here. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 159 , 817–889.     

Comparative study on the cranial morphology of Gymnallabes typus (Siluriformes: Clariidae) and their less anguilliform relatives,Clariallabes melas and Clarias gariepinus

We compare the cranial morphology of four fish species with an increasing anguilliformism in the following order: Clarias gariepinus, Clariallabes melas, Gymnallabes typus, and Channallabes apus. The main anatomical‐morphological disparities are the stepwise reduction of the skull roof along with the relative enlargement of the external jaw muscles, which occurred in each of them. Gymnallabes typus and C. apus lack a bony protection to cover the jaw muscles. The neurocranial bones of C. gariepinus, however, form a closed, broad roof, whereas the width of the neurocranium in C. melas is intermediate. Several features of the clariid heads, such as the size of the mouth and the bands of small teeth, may be regarded as adaptations for manipulating large food particles, which are even more pronounced in anguilliform clariids. The jaw musculature of G. typus is hypertrophied and attached on a higher coronoid process of the lower jaw, causing a larger adductive force. The hyomandibula interdigitates more strongly with the neurocranium and its dentition with longer teeth is posteriorly extended, closer to the lower jaw articulation. The anguilliform clariids also have their cranial muscles modified to enable a wider gape. The adductor mandibulae and the levator operculi extend more posteriorly, and the anterior attachment site of the protractor hyoidei dorsalis shifts toward the sagittal plane of the head. A phylogenetic analysis of the Clariidae, which is in progress, could check the validity of Boulenger's hypothesis that predecessors of the primitive fishes, such as Heterobranchus and most Clarias, would have evolved into progressively anguilliform clariids. J. Morphol. 240:169–194, 1999. © 1999 Wiley‐Liss, Inc.     

A new species of Ituglanis representing the southernmost record of the genus,with comments on phylogenetic relationships (Teleostei: Siluriformes: Trichomycteridae)

Ituglanis australis new species, is described from tributaries of the Laguna dos Patos and Río Uruguay, in Brazil and Uruguay. This represents the southernmost record of the genus and the first occurrence of a species of Ituglanis in those systems. It is distinguished from all its congeners, except Ituglanis parahybae and Ituglanis cahyensis, by its body pigmentation with three well‐defined dark brown stripes running along each flank. Ituglanis australis differs from I. parahybae and I. cahyensis in the pectoral‐ and pelvic‐fin ray counts, the pattern of the cephalic laterosensory system and the number of dorsal‐fin basal radials. The new species, as well as several other examined congeners, has the levator internus IV muscle attached to the dorsal face of the posttemporo‐supracleithrum; a condition that corroborates the inclusion of Ituglanis into a large trichomycterine clade that also includes Bullockia, Hatcheria, Scleronema and several species of Trichomycterus. Previous proposals of the affinities within Ituglanis are reviewed and, despite some advances, the phylogenetic relationships among species of the genus remain largely unknown.