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NCQ scaling of elliptic flow is studied in a non-equilibrium hadronization and freeze-out model from ideal, deconfined and chirally symmetric Quark Gluon Plasma (QGP), to final non-interacting hadrons. In this transition the quarks gain constituent quark mass while the background Bag-field breaks up. The constituent quarks then recombine into simplified hadron states, while chemical, thermal and flow equilibrium break down. Then the resulting temperatures and flow velocities of baryons and mesons will be different. In a simplified model, we reproduce the constituent quark number scaling.
Synchroidae Lacordaire, 1859 is a taxonomically and biologically poorly known group. In the present paper, diagnostic characters used to separate genera are analysed and the phylogenetic relationships within this family are preliminarily investigated. Results suggest that the characteristic Synchroa pangu Hsiao, Li, Liu & Pang, 2016 can be removed to establish a new genus, Thescelosynchroa gen. nov. The new combination, T. pangu (Hsiao, Li, Liu & Pang) gen. et comb. nov., is proposed. The definitions of Synchroa Newman, 1838 and Synchroina Fairmaire, 1898 are revised. Moreover, morphological analysis and character comparison also suggest that the familial placement of Mallodrya subaenea Horn, 1888 is questionable. Six species are re-examined and rediagnosed: Synchroa chinensis Nikitsky, 1999, S. elongatula Nikitsky, 1999, S. formosana Hsiao, 2015, S. melanotoides Lewis, 1895, S. punctata Newman, 1838 and Synchroina tenuipennis Fairmaire, 1898. The male of S. chinensis and the female of S. formosana are described for the first time. Synchroa elongatula and Synchroina tenuipennis are newly recorded from Laos and Indonesia, respectively. We also hypothesize that the Eastern Asian-North American disjunction of Synchroa could be connected to a Mid-Late Tertiary migration of plants via the Bering Land Bridge.
The Lycocerus hanatanii species group is revised, with the addition of seven taxa: L. araticollis (Fairmaire, 1897), L. nigripennis (Pic, 1938), L. griseopubens (Pic, 1928), L. yitingi Hsiao & Okushima sp. nov., L. aurantiacus Hsiao & Okushima sp. nov., L. evangelium Hsiao & Okushima sp. nov. and L. kintaroi Hsiao & Okushima sp. nov. Supplementary descriptions of the males of L. araticollis and L. griseopubens are provided. Lycocerus nigripennis (Pic, 1938) and L. pictus (Wittmer, 1983) are redescribed in detail. Each species is provided with photos or illustrations of genitalia of both sexes and abdominal ventrite VII of the female if available. Distribution maps and a key to the species of the L. hanatanii species group are presented. In addition, the monophyly of the L. hanatanii species group is supported based on a morphological phylogenetic analysis.
Non-standard errors
(2021)
In statistics, samples are drawn from a population in a data-generating process (DGP). Standard errors measure the uncertainty in sample estimates of population parameters. In science, evidence is generated to test hypotheses in an evidence-generating process (EGP). We claim that EGP variation across researchers adds uncertainty: non-standard errors. To study them, we let 164 teams test six hypotheses on the same sample. We find that non-standard errors are sizeable, on par with standard errors. Their size (i) co-varies only weakly with team merits, reproducibility, or peer rating, (ii) declines significantly after peer-feedback, and (iii) is underestimated by participants.