Systematic revision of the formerly monotypic genus Tanganikallabes (Siluriformes: Clariidae)

The monotypic genus Tanganikallabes, endemic to Lake Tanganyika, is a poorly known member of the family Clariidae. Examination of 142 specimens housed in museum collections has revealed the presence of at least two additional species in this genus. Tanganikallabes alboperca sp. nov. is distinguished from all congeners by the length of its pelvic fins, the presence of a depigmented vertical bar on the opercular margin, and a combination of additional morphometric (pectoral spine length, preanal length, body depth at anus) and meristic (dorsal and anal fin ray counts) characters. Tanganikallabes stewarti sp. nov. is distinguished from other Tanganikallabes species by having a relatively shorter, incomplete lateral line, and shallow body depth at the anus, as well as shorter prepelvic and preanal lengths, and a longer anal fin with a higher number of fin rays. Several morphological characters, as well as genetic data from cytochrome b (mitochondrial DNA) and 18S–ITS1–5.8S–ITS2–28S (ribosomal DNA), indicate that Tanganikallabes constitutes a monophyletic group within the Clariidae and support the recognition of additional species diversity. The monophyly of Tanganikallabes, coupled with the geographical isolation of this group to a single lake satisfy the requirements for its classification as a true species flock, the latest to be described from Lake Tanganyika. © 2012 The Linnean Society of London, Zoological Journal of the Linnean Society, 2012, 165 , 121–142.     

Characterization of Bacteroides Species Isolated From Soft Tissue Infections in Cats

A total of 77 strains of Gram negative anaerobes belonging to the genus Bacteroides and isolated from 60 subcutaneous abscesses and 10 cases of pyothorax in cats, have been examined morphologically and biochemically. Colony pigmentation, gas chromatography and biochemical analysis placed them into two major categories-those which produced pigmented colonies (Group 1) and those which failed to produce pigmented colonies after 14 d on laked blood agar (Group 2). All 29 strains in Group 1 produced acetic, propionic, isobutyric, butyric, isovaleric and succinic acids but failed to ferment carbohydrates, and were classified as B. asaccharolyticus. All organisms in Group 2 produced acetic, propionic, isobutyric, isovaleric and succinic acids and were divided into four categories based on indole production and bile tolerance. Designation to species was then decided on the basis of phenylacetic acid production and sugar fermentation tests. This sequence of analysis of results enabled confident speciation of some groups of these organisms despite some biochemical variation of the cat strains when compared to human type strains.     

The prevalence of viruses of honey bees in Britain

Adult individuals of honey bee colonies in Britain are commonly infected with several small RNA viruses. Black queen cell virus and bee virus Y are the commonest and occur most frequently about June, together with Nosema apis with which both viruses are intimately but independently associated. Bee virus X is less common than bee virus Y and showed no pronounced seasonal fluctuations in local surveys, but was detected mostly in winter and early spring. Sacbrood virus occurred in adults of most local colonies in summer, chronic paralysis virus and cloudy wing particle occurred commonly but without seasonal variations and acute paralysis occurred commonly throughout the active season of bees but does not multiply sufficiently to cause overt disease. Slow paralysis virus was rare.     

Recovery of plant DNA using a reciprocating saw and silica‐based columns

The time needed for hand grinding and the cost of commercially available extraction kits remain to be the major limitations in plant DNA extraction for many researchers. We present inexpensive techniques for (i) simultaneously machine grinding large numbers of plant samples for DNA extraction using a commercially available reciprocating saw; and (ii) DNA recovery using silica column‐based extractions similar to that used in some commercially available kits. Used together, these allow for the rapid recovery of plant DNA at relatively low cost. Furthermore, these methods appear to be widely applicable within plants with good yields recovered in test extractions across major plant groups (ferns, gymnosperms, monocots and eudicots).