A review of the genus Berosus Leach of Cuba (Coleoptera,Hydrophilidae)

The Cuban fauna of the genus Berosus Leach, 1817 is reviewed based on newly collected material as well as historical and type specimens. Nine species are recognized, including three recorded from Cuba for the first time: Berosus infuscatus LeConte, 1855, Berosus interstitialis Knisch, 1924 (= Berosus stribalus Orchymont, 1946 syn. n.) and Berosus metalliceps Sharp, 1882. Only one of the nine Cuban species, Berosus chevrolati, remains endemic to Cuba, as two other species previously considered as endemic to Cuba are recorded from elsewhere: Berosus quadridens from Mexico and Central America and Berosus trilobus from the Dominican Republic. Notes on biology and Cuban distribution are provided for all nine species. Berosus quadridens Chevrolat, 1863, stat. restit. is removed from synonym with Berosus truncatipennis and considered a valid species.     

Schistosoma japonicum Eggs Induce a Proinflammatory,Anti-Fibrogenic Phenotype in Hepatic Stellate Cells

Hepatic fibrosis induced by egg deposition is the most serious pathology associated with chronic schistosomiasis, in which the hepatic stellate cell (HSC) plays a central role. While the effect of Schistosoma mansoni eggs on the fibrogenic phenotype of HSCs has been investigated, studies determining the effect of eggs of S . japonicum on HSCs are lacking. Disease caused by S . japonicum is much more severe than that resulting from S. mansoni infection so it is important to compare the pathologies caused by these two parasites, to determine whether this phenotype is due to the species interacting differently with the mammalian host. Accordingly, we investigated the effect of S . japonicum eggs on the human HSC cell line, LX-2, with and without TGF-β (Transforming Growth Factor beta) co-treatment, so as to determine the impact on genes associated with fibrogenesis, inflammation and matrix re-organisation. Activation status of HSCs was assessed by αSMA (Alpha Smooth Muscle Actin) immunofluorescence, accumulation of Oil Red O-stained lipid droplets and the relative expression of selected genes associated with activation. The fibrogenic phenotype of HSCs was inhibited by the presence of eggs both with or without TGF-β treatment, as evidenced by a lack of αSMA staining and reduced gene expression of αSMA and Col1A1 (Collagen 1A1). Unlike S. mansoni-treated cells, however, expression of the quiescent HSC marker PPAR-γ (Peroxisome Proliferator-Activated Receptor gamma) was not increased, nor was there accumulation of lipid droplets. In contrast, S . japonicum eggs induced the mRNA expression of MMP-9 (Matrix Metalloproteinase 9), CCL2 (Chemokine (C-C motif) Ligand 2) and IL-6 (Interleukin 6) in HSCs indicating that rather than inducing complete HSC quiescence, the eggs induced a proinflammatory phenotype. These results suggest HSCs in close proximity to S . japonicum eggs in the liver may play a role in the proinflammatory regulation of hepatic granuloma formation.     

A revision of the Cautires obsoletus species group from Java (Coleoptera,Lycidae)

The Javanese fauna of the species group Cautires obsoletus is revised. Altogether, eight Javanese species were classified in the group; five of them are proposed to be junior subjective synonyms: Cautires fruhstorferi Dudkova & Bocak, 2010, a replacement name of Bulenides lineatus Pic, 1921, Cautires javanicus Bourgeois, 1883, Cautires inhumeralis (Pic, 1921), Cautires nigromaculatus (Pic, 1925), and Cautires pudicus (Kleine, 1931) (all synonymized to Cautires obsoletus Waterhouse, 1879). Three Javanese species are redescribed: Cautires apicalis (Pic, 1925), Cautires obsoletus (Waterhouse, 1878), and Cautires singularithorax (Pic, 1925). Cautires apicalis (Pic, 1925) is removed from the synonymy of Cautires corporaali (Pic, 1921) and reinstated as a valid name. Three new species are proposed: Cautires walteri sp. n., Cautires taoi sp. n., and Cautires sukosarensis sp. n. All species are keyed and principal diagnostic characters are illustrated. The distribution and relationships to Cautires fauna of other Great Sundas islands are briefly discussed.     

A review of the genus Monema Walker in China (Lepidoptera,Limacodidae)

Four species and one subspecies of the genus Monema Walker, 1855 are recognized from China, in which Monema tanaognatha Wu & Pan sp. n. is described as new, Monema coralina Dudgeon, 1895 and Monema meyi Solovyev & Witt, 2009 are newly recorded for China. The female of Monema meyi is reported for the first time. Monema nigrans de Joannis, 1901 and Monema melli Hering, 1931 are synonymized with Monema flavescens Walker, 1855. Cnidocampa rubriceps Matsumura, 1931 is regarded here as a subspecies of Monema flavescens Walker, 1855. The photographs of moths and their genitalia are given. A key to the species of the genus is provided.     

A new species of Perinereis (Polychaeta,Nereididae) from Florida,USA, with a key to all Perinereis from the?American continent

Specimens belonging to a new species of Perinereis Kinberg, 1865 were collected fromnatural oyster reefs in an estuarine environmenton Florida’s southwest coast. The genus Perinereis includes more than 70 species, of which, Perinereis aibuhitensis (Grube, 1878), Perinereis brevicirrata (Treadwell, 1920), Perinereis camiguinoides (Augener, 1922), Perinereis jascooki Gibbs, 1972, Perinereis kuwaitensis Mohammad, 1970, Perinereis singaporiensis (Grube, 1878), Perinereis vancaurica (Ehlers, 1868) and the new species have two short bars on Area VI and notopodial dorsal ligules that are not greatly expanded. The most geographically close species is Perinereis brevicirrata. The new species can be distinguished from Perinereis brevicirrata by the absence of a notopodial prechaetal lobe, Area V with 3 cones in a triangle, and Area VII-VIII with two well-defined rows of 33 paragnaths, the basal row having longer paragnaths in relation to the distal ones. The new species resembles Perinereis singaporiensis based on the absence of notopodial prechaetal lobe; however, the two species differ in some morphological characteristics such as tentacular cirri length, shape of dorsal notopodial ligules, and falciger blades. A key to all American species of Perinereis is included.     

Effect of Starvation on the Endocytic Pathway in Dictyostelium Cells

Dictyostelium discoideum amoebae have been used extensively to study the structure and dynamics of the endocytic pathway. Here, we show that while the general structure of the endocytic pathway is maintained in starved cells, its dynamics rapidly slow down. In addition, analysis of apm3 and lvsB mutants reveals that the functional organization of the endocytic pathway is profoundly modified upon starvation. Indeed, in these mutant cells, some of the defects observed in rich medium persist in starved cells, notably an abnormally slow transfer of endocytosed material between endocytic compartments. Other parameters, such as endocytosis of the fluid phase or the rate of fusion of postlysosomes to the cell surface, vary dramatically upon starvation. Studying the endocytic pathway in starved cells can provide a different perspective, allowing the primary (invariant) defects resulting from specific mutations to be distinguished from their secondary (conditional) consequences.Dictyostelium discoideum is a widely used model organism for studying the organization and function of the endocytic pathway. In Dictyostelium, the organization of the endocytic pathway is similar to that in higher eukaryotes. The pathway in Dictyostelium can be divided into four steps (see Fig. S1 in the supplemental material): uptake at the plasma membrane of particles and medium, transfer through early acidic endocytic compartments (lysosomes), passage into less acidic postlysosomes (PLs), and finally, exocytosis of undigested materials (17, 20). Thus, Dictyostelium recapitulates many of the functions of the endocytic pathway in mammalian cells, including some features observed in most cell types (lysosome biogenesis) and some observed only in specialized cells (phagocytosis, macropinocytosis, and lysosome secretion).Dictyostelium amoebae live in the soil, where they feed by ingesting and digesting other microorganisms. In addition, axenic laboratory strains can macropinocytose medium to ensure their growth. Accordingly, both in natural situations and in laboratory settings, the endocytic pathway plays a key role in the acquisition of nutrients by Dictyostelium cells. In agreement with this notion, several observations suggest that the physiology of the endocytic pathway is sensitive to nutrient availability. In particular, starvation induces secretion of lysosomal enzymes by an unknown mechanism (11). The morphology of the endocytic pathway is also sensitive to nutritional cues, as shown for example by the observation that formation of multilamellar endosomes is enhanced in cells fed with bacteria (18).Here, we analyzed the effect of starvation on the organization as well as the dynamics of the endocytic pathway. We found that, while the overall organization was not extensively modified in starved cells, the dynamics of endocytic compartments were altered. Moreover, analysis of two specific knockout mutants, the apm3 (6) and lvsB (8) strains, revealed that their phenotype was profoundly altered upon starvation, providing further insight about the role of Apm3 and LvsB in the endocytic pathway.     

A new species of Haplosporidium Caullery & Mesnil, 1899 in the marine false limpet Siphonaria lessonii (Gastropoda: Siphonariidae) from Patagonia

A new species of Haplosporidium Caullery & Mesnil, 1899 parasitising the pulmonate gastropod Siphonaria lessonii Blainville in Patagonia, Argentina, is described based on morphological (scanning and transmission electron microscopy) and sequence (small subunit ribosomal RNA gene) data. Different stages of sporulation were observed as infections disseminated in the digestive gland. Haplosporidium patagon n. sp. is characterised by oval or slightly subquadrate spores with an operculum that is ornamented with numerous short digitiform projections of regular height, perpendicular to and covering its outer surface. The operculum diameter is slightly larger than the apical diameter of the spore. Neither the immature nor mature spores showed any kind of projections of the exosporoplasm or of the spore wall. Regarding phylogenetic affinities, the new species was recovered as sister to an undescribed species of Haplosporidium Caullery & Mesnil, 1899 from the polychaete family Syllidae Grube from Japanese waters. The morphological characters (ornamentation of the operculum, spore wall structure, shape and size of spores, and the lack of spore wall projections) corroborate it as an as yet undescribed species of Haplosporidium and the first for the phylum in marine gastropods of South America. Siphonaria lessonii is the only known host to date.     

Corrections to Agrilus related species–group names in the world catalogue of Bellamy and new substitute names for Agrilus species–group homonyms

The work treats 52 species–group names related to genus Agrilus incorrectly cited in the world catalogue of Bellamy (2008). The name dimorphus Théry, 1941 from the genus Aphanisticus and mulleri Théry, 1925 from the genus Australodraco are also treated. Four primary or secondary homonyms are replaced by substitute names. Most of the proposed changes refer to the availability, validity, spelling and authorship of the names. The following new nomenclatural acts are proposed: Four new substitute names for homonyms: gola Jendek for filiformis Gory & Laporte, 1839 not Herbst, 1801; lukesi Obenberger, 1936 for modicus Kerremans, 1892 not Solier, 1833; thomsoni Jendek for impressipennis Thomson not Uhler, 1855; walkerianus Jendek (Aphanisticus) for sulcicollis Walker not Lacordaire, 1835. New synonyms: turei Curletti, 2002 is an objective synonym of thurei Curletti, 1996. Lectotype designations: A lectotype is designated for Agrilus dualaecola Obenberger, 1923.     

Talaromyces columbinus sp. nov., and Genealogical Concordance Analysis in Talaromyces Clade 2a

During the course of mold surveys, a set of Talaromyces isolates were obtained that did not fit any described species. Phenotypic examination of these isolates showed that they were similar to T. piceus but differed in some growth characteristics. Multilocus DNA sequence data were obtained for the new isolates and some related species in the broader, more inclusive clade, and the data were analyzed using genealogical concordance. The new isolates are described as Talaromyces columbinus. From analysis of the related species, Penicillium rugulosum var. atricolum is given species status in Talaromyces as T. atricola. Penicillium tardum and P. chrysitis were showed to be synonyms of T. rugulosus. Penicillium scorteum and T. phialosporus were showed to be conspecific and under the rule of priority T. scorteus is the proper name for isolates previously known as T. phialosporus. Talaromyces wortmanii was showed to be distinct from Penicillium concavorugulosum and T. variabilis but the relationship of the latter two species remains unresolved. Examination of ITS sequences from GenBank showed that T. columbinus has previously been reported from human lung infections under the name Penicillium piceum.     

Description of third instar larvae of Ceratitis fasciventris,C. anonae,C. rosa (FAR complex) and C. capitata (Diptera,Tephritidae)

Third instar larvae of members of the Ceratitis FAR complex, including Ceratitis fasciventris (Bezzi), Ceratitis anonae Graham, and Ceratitis rosa Karsch are described and compared with those of Ceratitis capitata (Wiedemann). Diagnostic characters, such as presence vs. absence of a secondary tooth on the mandibles, previously used to separate Ceratitis capitata from Ceratitis rosa, are shown to vary in each species. Significant variation in diagnostic morphological characters among populations of Ceratitis rosa from east and south Africa is documented; however, the differences are not simply congruent with the R1 and R2 designations based on other studies. Quantitative measures of numerous morphological characters are consistently smaller in the larvae of Ceratitis fasciventris and distinguish them from other species of the FAR complex. Larvae of Ceratitis capitata can be distinguished from those of the FAR complex by characters such as absence of accessory plates of the oral ridges, the shape of the anterior spiracle, and the pattern of dorsal spinules. Previous studies indicated that absence of accessory lobes separate the genus Ceratitis from Bactrocera, but this is shown to be incorrect, as accessory lobes are in fact present in several species of Ceratitis.     

A revision of the Afrotropical spider genus Cambalida Simon, 1909 (Araneae,Corinnidae)

The non-mimetic Afrotropical spider genus Cambalida Simon, 1909, placed within a subfamily of predominantly ant-mimicking spiders (Araneae: Corinnidae: Castianeirinae), is revised. Three species are transferred from Castianeira Keyserling, 1879 to Cambalida: Cambalida deminuta (Simon, 1909), comb. n., Cambalida fulvipes (Simon, 1896), comb. n. and Cambalida loricifera (Simon, 1885), comb. n.. A fourth species, Cambalida fagei (Caporiacco, 1939), comb. n., is transferred from Brachyphaea Simon, 1895 to Cambalida. Two species, Castianeira depygata Strand, 1916, syn. n. and Cambalida mestrali Lessert, 1921, syn. n., are considered junior synonyms of Cambalida fulvipes. The males of Cambalida deminuta and Cambalida loricifera are redescribed and their unknown females are described for the first time. The female and male of Cambalida fulvipes and Cambalida coriacea Simon, 1909 are also redescribed. The type material of the type species of the genus, Cambalida insulana Simon, 1909 from Pagalu (Annobon) Island, is lost, and only immature specimens have been subsequently collected from a nearby island. The species is regarded as a nomen dubium until fresh adult material can be collected. A replacement name, Cambalida simoni nom. n. is proposed for Cambalida fulvipes Simon, 1909, the latter being a secondary junior homonym of Cambalida fulvipes (Simon, 1896). The type material of this species is also lost and it is too considered nomen dubium. The following new species are described: Cambalida compressa sp. n. from West Africa, Cambalida dippenaarae sp. n. from southern Africa, Cambalida griswoldi sp. n. and Cambalida lineata sp. n. from Madagascar, and Cambalida unica sp. n. from Cameroon. Notes are provided on the biology of each species and the distribution of the genus in the Afrotropical Region.