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The inclusive charged particle transverse momentum distribution is measured in proton–proton collisions at s=900 GeV at the LHC using the ALICE detector. The measurement is performed in the central pseudorapidity region (|η|<0.8) over the transverse momentum range 0.15<pT<10 GeV/c. The correlation between transverse momentum and particle multiplicity is also studied. Results are presented for inelastic (INEL) and non-single-diffractive (NSD) events. The average transverse momentum for |η|<0.8 is 〈pT〉INEL=0.483±0.001 (stat.)±0.007 (syst.) GeV/c and 〈pT〉NSD=0.489±0.001 (stat.)±0.007 (syst.) GeV/c, respectively. The data exhibit a slightly larger 〈pT〉 than measurements in wider pseudorapidity intervals. The results are compared to simulations with the Monte Carlo event generators PYTHIA and PHOJET.
Men and women differ substantially regarding height, weight, and body fat. Interestingly, previous work detecting genetic effects for waist-to-hip ratio, to assess body fat distribution, has found that many of these showed sex-differences. However, systematic searches for sex-differences in genetic effects have not yet been conducted. Therefore, we undertook a genome-wide search for sexually dimorphic genetic effects for anthropometric traits including 133,723 individuals in a large meta-analysis and followed promising variants in further 137,052 individuals, including a total of 94 studies. We identified seven loci with significant sex-difference including four previously established (near GRB14/COBLL1, LYPLAL1/SLC30A10, VEGFA, ADAMTS9) and three novel anthropometric trait loci (near MAP3K1, HSD17B4, PPARG), all of which were significant in women, but not in men. Of interest is that sex-difference was only observed for waist phenotypes, but not for height or body-mass-index. We found no evidence for sex-differences with opposite effect direction for men and women. The PPARG locus is of specific interest due to its link to diabetes genetics and therapy. Our findings demonstrate the importance of investigating sex differences, which may lead to a better understanding of disease mechanisms with a potential relevance to treatment options.
The ischnoceran chewing lice known from bulbuls are discussed and revised, and 18 new species are described. These are: Brueelia celer sp. nov. from Pycnonotus cafer bengalensis Blyth, 1845 and Pycnonotus cafer primrosei Deignan, 1949; Brueelia colindalei sp. nov. from Hemixos castanonotus canipennis Seebohm, 1890; Brueelia doisuthepensis sp. nov. from Alophoixus ochraceus ochraceus (Moore, 1858); Brueelia galeata sp. nov. from Alophoixus pallidus henrici (Oustalet, 1896); Brueelia hermetica sp. nov. from Pycnonotus barbatus layardi Gurney, 1879; Brueelia leiae sp. nov. from Alophoixus flaveolus burmanicus (Oates, 1899); Brueelia robertrankini sp. nov. from Pycnonotus jocosus jocosus (Linnaeus, 1758) and Pycnonotus jocosus pattani Deignan, 1948; Brueelia yunnanensis sp. nov. from Ixos mcclellandii similis (Rothschild, 1921); Guimaraesiella brunneomarginata sp. nov. from Pycnonotus goiaver samarensis Rand & Rabor, 1960 and Pycnonotus goiaver personatus Hume, 1873; Guimaraesiella caligogularis sp. nov. from Pycnonotus plumosus plumosus Blyth, 1845 and Alophoixus bres tephrogenys (Jardine & Selby, 1833); Guimaraesiella cinnamomea sp. nov. from Iole propinqua propinqua (Oustalet, 1903) and Iole viridescens cinnamomeoventris Baker, 1917; Guimaraesiella ixi sp. nov. from Ixos mcclellandii peracensis (Hartert & Butler, 1898); Guimaraesiella lorica sp. nov. from Hypsipetes leucocephalus nigerrimus Gould, 1863; Guimaraesiella mayoensis sp. nov. from Hypsipetes everetti everetti (Tweeddale, 1877); Guimaraesiella phlaoalopha sp. nov. from Alophoixus pallidus henrici (Oustalet, 1896); Philopteroides holosternus sp. nov. from Pycnonotus goiavier goiavier (Scopoli, 1786); Philopteroides longiclypeatus sp. nov. from Hypsipetes everretti samarensis Rand & Rabor, 1959; Philopteroides haerixos sp. nov. from Ixos mcclellandii holtii (Swinhoe, 1861) and Alophoixus pallidus henrici (Oustalet, 1896). The following new host records are provided: Hemixos castanonotus canipennis Seebohm, 1890, for Guimaraesiella flavala (Najer & Sychra in Najer et al., 2012); Pycnonotus blanfordi conradi (Finsch in Finsch & Conrad, 1873) for Philopteroides cucphuongensis Mey, 2004. Philopterus cucphuongensis is tentatively redescribed and illustrated based on specimens from a non-type host species. The species descriptions of the following species are amended slightly, based on re-examinations of type specimens: Brueelia alophoixi Sychra in Sychra et al., 2009; Guimaraesiella cucphuongensis (Najer & Sychra in Najer et al., 2012); Guimaraesiella flavala (Najer & Sychra in Najer et al., 2012). We propose to move Philopterus hiyodori Uchida, 1949, to the genus Craspedorrhynchus Kéler, 1938. The species Sturnidoecus acutifrons (Uchida, 1949) and Penenirmus guldum (Ansari, 1955) are considered species inquirenda. An updated checklist of ischnoceran lice known from bulbuls is provided, as well as a key to all ischnoceran species known from bulbuls.
The geographical range of the typically host-specific species of chewing lice (Phthiraptera) is often assumed to be similar to that of their hosts. We tested this assumption by reviewing the published records of twelve species of chewing lice parasitizing wild and domestic chicken, one of few bird species that occurs globally. We found that of the twelve species reviewed, eight appear to occur throughout the range of the host. This includes all the species considered to be native to wild chicken, except Oxylipeurus dentatus (Sugimoto, 1934). This species has only been reported from the native range of wild chicken in Southeast Asia and from parts of Central America and the Caribbean, where the host is introduced. Potentially, this discontinuous distribution is due to a low tolerance for dry environments, possibly exacerbated by competitive exclusion by Cuclotogaster heterographus (Nitzsch, 1866). Our examinations of O. dentatus also revealed that this species differs significantly from other species of Oxylipeurus in the male and female genitalia, head structure and chaetotaxy, and other morphological characters. We therefore here erect the monotypic genus Gallancyra gen. nov. for O. dentatus, and redescribe the type species.
Four new species of Brueelia Kéler, 1936 are described and illustrated. All of them parasitize African endemic host species in the families Passeridae, Ploceidae, and Estrildidae (Passeriformes). They are: Brueelia pofadderensis sp. nov. ex Passer melanurus damarensis Reichenow, 1902 and P. m. vicinus Clancey, 1958; B. semiscalaris sp. nov. ex Granatina granatina (Linnaeus, 1758); B. sima sp. nov. ex Malimbus nitens (Gray, 1831); B. terpsichore sp. nov. ex Euplectes jacksoni (Sharpe, 1891) and E. progne delamerei (Shelley, 1903). In addition, Brueelia bicurvata (Piaget, 1880) is redescribed and reillustrated from non-type material. A summary of all published records of lice in the Brueelia complex from Africa since 1980 is provided. We also estimate the unknown diversity of African species of Brueelia based on an index of host specificity calculated for each host family independently. The unknown diversity is estimated to be over 1000 species of Brueelia from African hosts, compared to the < 50 species in this genus currently recorded from Africa.
The chewing louse species Lipeurus megalops Piaget, 1880, is redescribed and illustrated. This species has previously been placed in the genus Oxylipeurus Mjöberg, 1910, but marked differences in preantennal structure, male and female genitalia, abdominal chaetotaxy, and structure of abdominal plates indicate that this species is not closely related to other species in this genus. We therefore erect a new genus, Calidolipeurus gen. nov. for this species. Calidolipeurus is presently monotypic, containing only Calidolipeurus megalops gen. et comb. nov. We also provide a preliminary key to the Oxylipeurus-complex.
We describe and illustrate eight new species of chewing lice in the genus Philopterus Nitzsch, 1818, parasitic on hosts in the bird families Cardinalidae, Chloropseidae, Hirundinidae, Icteridae, Motacillidae, Paridae, and Vangidae from China, Peru, South Africa, Thailand, and the USA. They are: Philopterus coriaceus sp. nov. from Molothrus oryzivorus oryzivorus (Gmelin, 1788); P. hebes sp. nov. from Chloropsis aurifrons inornata Kloss, 1918 and C. cochinchinensis kinneari Hall & Deignan, 1956; P. micropunctatus sp. nov. from Anthus hodgsoni Richmond, 1907; P. afropari sp. nov. from Melaniparus cinerascens cinerascens (Vieillot, 1818); P. pseudhirundo sp. nov. from Pseudhirundo griseopyga Sundevall, 1850; P. sinensis sp. nov. from Hemipus picatus capitalis (Horsfield, 1840); P. stansburyensis sp. nov. from Pheucticus melanocephalus melanocephalus (Swainson, 1827); and P. trepostephanus sp. nov. from Tephrodornis virgatus fretensis Robinson & Kloss, 1920 and T. v. mekongensis Meyer de Schauensee, 1946. Philopterus hebes sp. nov. constitutes the first record of the genus Philopterus from the Chloropseidae. We also provide some notes on the morphology and status of Cypseloecus Conci, 1941.
The genus Painjunirmus Ansari, 1947 is resurrected from synonymy with Brueelia Kéler, 1936, and considered a subgenus of Brueelia Kéler, 1936. A formal redescription and diagnosis for Painjunirmus is given. Four of the five previously described species of Painjunirmus are redescribed and illustrated: Brueelia (Painjunirmus) brevipennis Ansari, 1956, from Argya squamiceps squamiceps (Cretzschmar, 1826); Brueelia (Painjunirmus) chilchil Ansari, 1955, from Argya caudata eclipes (Hume, 1877); Brueelia (Painjunirmus) magnini Ansari, 1956a, from Argya fulva acaciae (Lichtenstein, 1823); Brueelia (Painjunirmus) pengya (Ansari, 1947) from Argya striata sindiana (Ticehurst, 1920) and A. s. striata (Dumont, 1823). The species Brueelia (Painjunirmus) parvus (Mey, 2017) is discussed. The species Brueelia (Painjunirmus) alba sp. nov. is described from a Nepalese population of Argya striata striata (Dumont, 1823). A neotype is designated for Brueelia chilchil Ansari, 1956. A key to almost all species of the subgenus Painjunirmus is provided.
The ischnoceran louse genus Dictyocotes Kéler, 1940, has long been considered a synonym of Goniocotes Burmeister, 1838, but the genus has never been revised. Here, the relationships within and between Goniocotes and Dictyocotes are discussed, and the latter genus is resurrected from synonymy. Both genera are redescribed, and four new species of lice are described and illustrated. They are: Dictyocotes furcatus sp. nov. ex Lophophorus lhuysii Geoffroy Saint-Hilaire, 1866; Goniocotes cacumentalis sp. nov. ex Tetraogallus tibetanus Gould, 1854; Goniocotes caoi sp. nov. ex Chrysolophus pictus (Linnaeus, 1758); Goniocotes sarissa sp. nov. ex Tragopan caboti (Gould, 1857). The altitudinal distribution of these two genera is discussed, and appears to indicate a division between a primarily low-altitude Goniocotes and an exclusively high-altitude Dictyocotes. The driving force behind this division is unknown, but unlikely to be based on host associations.