805 research outputs found

    Two new Australian fungus-feeding thrips in two new Plectrothripini genera (Thysanoptera, Phlaeothripinae)

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    Two new genera are erected of plectrothripine Phlaeothripidae from northern Australia, each based on a single species. One has a long stout projection ventrally on the second antennal segment, the other has a unique arrangement of the dorsal facets of the compound eyes. In both of them the thoracic ventral sclerites are extensively eroded. The tribe Plectrothripini is one of the few apparently discrete lineages within the large and complex subfamily Phlaeothripinae (Dang et al. 2014). The species in this Tribe are all fungus-feeders on dead branches, and the group is found in the tropics worldwide. Okajima (1981) provided an extensive, illustrated account of the Plectrothripini, recognising 10 genera and almost 50 species, to which Tyagi et al. (2016) added one further species. Six of these genera remain monotypic, with two genera each comprising five or six species, and Plectrothrips itself with about 30 species. This asymmetry of taxon distribution, with a high proportion of monotypic genera, is due to the presence of certain characters in unusual autapomorphic states. Phylogenetic relationships within the tribe are further confused here through the diagnosis of two new monotypic genera for species from the tropical north of Australia. One of these new species has a bizarre projection ventrally on the second antennal segment (Fig. 5), whilst the other has the structure of the compound eyes unique amongst Phlaeothripidae (Figs 7, 8). Membership of the Tribe Plectrothripini is fairly clear, with the species sharing most of the following character states as indicated by Okajima (1981): antennae 8-segmented, segment II with the campaniform sensillum on the basal half, III–IV with a variable number of short, stout sense cones, VIII elongate with narrow base. Head with posterior ocelli close to compound eyes. Pronotum commonly with sclerotised plate eroded and reduced; prosternal basantra absent; fore tarsal tooth large; apex of hind tibiae commonly with stout setae. Pelta wide at base, tergite II eroded laterally; sternites often with reticulate glandular areas

    Convoluted maxillary stylets among Australian Thysanoptera Phlaeothripinae associated mainly with Casuarinaceae trees

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    The diversity is reviewed of Phlaeothripinae in Australia with unusually long or convoluted maxillary stylets. This comprises a total of 28 species in eight genera, including Enigmathrips carnarvoni gen et sp.n., Adrothrips latrarei sp.n., A. lihongae sp.n., A. madiae sp.n., A mitcheli sp.n., A. vernoni sp.n., and A. westoni sp.n., also Heligmothrips exallus sp.n., H. macropus sp.n., H. narrabri sp.n. and H. xanthoskelus sp.n., and Iotatubothrips daguilari sp.n. Among Phlaeothripinae, such exceptionally long feeding stylets are known only from Australia and have evolved independently within the unrelated genera Adrothrips and Heligmothrips in association with the green branchlets of Casuarinaceae species. A few species appear to have diverged in their feeding habits and have adapted to fungal-hyphal feeding on the trunks of trees

    Genera of fungivorous Phlaeothripinae (Thysanoptera) from dead branches and leaf-litter in Australia

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    An illustrated key is provided for the identification of 39 genera of Thysanoptera-Phlaeothripinae with species that live in association with dead branches and leaf-litter in Australia and are considered to be fungus-feeding. Seven of these gen-era are not previously recorded from this continent, including un-named species of Deplorothrips, Malacothrips, Mystro-thrips, Preeriella and Tylothrips, together with Azaleothrips lepidus Okajima and Terthrothrips ananthakrishnani Kudo. A brief generic diagnosis is provided for each genus, together with comments on systematic problems and numbers of species. Copyright © 2013 Magnolia Press

    Disfluency in dialogue:an intentional signal from the speaker?

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    Disfluency is a characteristic feature of spontaneous human speech, commonly seen as a consequence of problems with production. However, the question remains open as to why speakers are disfluent: Is it a mechanical by-product of planning difficulty, or do speakers use disfluency in dialogue to manage listeners' expectations? To address this question, we present two experiments investigating the production of disfluency in monologue and dialogue situations. Dialogue affected the linguistic choices made by participants, who aligned on referring expressions by choosing less frequent names for ambiguous images where those names had previously been mentioned. However, participants were no more disfluent in dialogue than in monologue situations, and the distribution of types of disfluency used remained constant. Our evidence rules out at least a straightforward interpretation of the view that disfluencies are an intentional signal in dialogue. © 2012 Psychonomic Society, Inc

    Engineering the Controlled Assembly of Filamentous Injectisomes in E. coli K-12 for Protein Translocation into Mammalian Cells.

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    Bacterial pathogens containing type III protein secretion systems (T3SS) assemble large needle-like protein complexes in the bacterial envelope, called injectisomes, for translocation of protein effectors into host cells. The application of these molecular syringes for the injection of proteins into mammalian cells is hindered by their structural and genomic complexity, requiring multiple polypeptides encoded along with effectors in various transcriptional units (TUs) with intricate regulation. In this work, we have rationally designed the controlled expression of the filamentous injectisomes found in enteropathogenic Escherichia coli (EPEC) in the nonpathogenic strain E. coli K-12. All structural components of EPEC injectisomes, encoded in a genomic island called the locus of enterocyte effacement (LEE), were engineered in five TUs (eLEEs) excluding effectors, promoters and transcriptional regulators. These eLEEs were placed under the control of the IPTG-inducible promoter Ptac and integrated into specific chromosomal sites of E. coli K-12 using a marker-less strategy. The resulting strain, named synthetic injector E. coli (SIEC), assembles filamentous injectisomes similar to those in EPEC. SIEC injectisomes form pores in the host plasma membrane and are able to translocate T3-substrate proteins (e.g., translocated intimin receptor, Tir) into the cytoplasm of HeLa cells reproducing the phenotypes of intimate attachment and polymerization of actin-pedestals elicited by EPEC bacteria. Hence, SIEC strain allows the controlled expression of functional filamentous injectisomes for efficient translocation of proteins with T3S-signals into mammalian cells
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