Nomenclatural faux pas for Speyeria atlantis greyi Moeck, 1950 (Lepidoptera: Nymphalidae)

Nomenclatural errors associated with the nymphalid butterfly, Speyeria atlantis greyi Moeck, have persisted in the literature and electronic databases. We present here a synonymy of the various combinations and misspellings associated with it and clearly indicate the correct name and spelling based on Moecks (1950) original description. Additionally, color images of the holotype and allotype specimens are published herein for the first time

Records for Bittacus Hangingflies and Panorpa Scorpionflies (Mecoptera: Bittacidae and Panorpidae) in Florida

We provide new county records for four species of panorpids (Panorpa americana Swederus, Panorpa lugubris Swederus, Panorpa sp. undetermined, and one undescribed species from the Panorpa rufescens Rambur species group) and two species of bittacids (Bittacus pilicornis Westwood, Bittacus punctiger Westwood), and call attention to a previously published county record for another species, Panorpa rufa Gray, in Florida. Additionally, we reject a previously published record for the scorpionfly Panorpa claripennis Hine in Florida, which we overlooked in our 2008 preliminary checklist of Florida mecopterans. The record for P. lugubris in Miami-Dade County is the southernmost record for any panorpid in the continental United States

Preliminary Checklist of the Mecoptera of Florida: Earwigflies, Hangingflies, and Scorpionflies

We provide the first species checklist of Mecoptera indigenous to Florida, based upon preliminary data gathered primarily from specimens housed in the Florida State Collection of Arthropods. There are 11 described and one undescribed species of mecopterans, representing three families, inhabiting the state of Florida. These include the recently discovered meropeid (earwigfly), Merope tuber Newman, four species of bittacids (hangingflies), represented by the genus Bittacus Latreille, and 7 species (one undescribed) of panorpids (scorpionflies), represented by the genus Panorpa Linnaeus. We are not certain if one of these, Bittacus texanus Banks, is indigenous, represents a nonindigenous occurrence, or is simply erroneous. Two of the species on our list, Bittacus stigmaterus Say and Panorpa venosa Westwood, represent first state records and one species, Panorpa floridana Byers, is endemic. Six of the species which have been recorded in Florida, M. tuber, Bittacus punctiger Westwood, Panorpa rufa Gray, Panorpa pachymera Byers, Panorpa lugubris Swederus and P. venosa, represent the southernmost records for these species in the continental United States. Perceived diversity and abundance of mecopteran species in Florida are limited by climate, biogeography, and collection bias

Rediscovery of the Florida Scorpionfly, Panorpa floridana Byers (Mecoptera: Panorpidae)

We describe the rediscovery of the Florida scorpionfly, Panorpa floridana Byers (Mecoptera: Panorpidae), at Gold Head Branch State Park, Clay County, Florida, based upon a single, living, adult specimen photographed on 4 November 2010. The hardcopy photographic prints and electronic digital images of this panorpid are the first vouchers for P. floridana in 28 years, the only observation of a living specimen, and the sixth individual known of this seemingly rare Florida endemic

Etymology of the earwigfly, \u3ci\u3eMerope tuber\u3c/i\u3e Newman (Mecoptera: Meropeidae): Simply dull or just inscrutable?

The naturalist Edward Newman did not provide an etymology for the mecopteran Merope tuber when he described it in 1838. In 1872 Asa Fitch asserted that the genus was named after Merope one of the Pleiades sisters of Greek mythology; however, he provided no reason for his assumption. We researched several etymological alternatives. We concur with Fitch and conclude that Newman did indeed name the genus Merope after the dullest of the Pleiades sisters

Current disposition of earwigflies, \u3ci\u3eMerope tuber\u3c/i\u3e Newman and \u3ci\u3eAustromerope poultoni\u3c/i\u3e Killington (Mecoptera: Meropeidae), in the Florida State Collection of Arthropods

We provide the current holdings of Meropeidae in the Florida State Collection of Arthropods (FSCA). To date, FSCA holds a well-curated collection of extant meropeids representing 17 U.S. states and Western Australia (n = 316 Merope tuber Newman, five Austromerope poultoni Killington). Merope tuber records from Vermont, Texas, and South Carolina are published here for the first time. A total of 298 pinned M. tuber and four pinned A. poultoni; six M. tuber specimens preserved in 95% ethanol; and 12 M. tuber and one A. poultoni sputter-coated with gold-palladium for SEM are available for researchers interested in studying this unique family of insects

Enskog Theory for Polydisperse Granular Mixtures. I. Navier-Stokes order Transport

A hydrodynamic description for an $s$-component mixture of inelastic, smooth hard disks (two dimensions) or spheres (three dimensions) is derived based on the revised Enskog theory for the single-particle velocity distribution functions. In this first portion of the two-part series, the macroscopic balance equations for mass, momentum, and energy are derived. Constitutive equations are calculated from exact expressions for the fluxes by a Chapman-Enskog expansion carried out to first order in spatial gradients, thereby resulting in a Navier-Stokes order theory. Within this context of small gradients, the theory is applicable to a wide range of restitution coefficients and densities. The resulting integral-differential equations for the zeroth- and first-order approximations of the distribution functions are given in exact form. An approximate solution to these equations is required for practical purposes in order to cast the constitutive quantities as algebraic functions of the macroscopic variables; this task is described in the companion paper.Comment: 36 pages, to be published in Phys. Rev.

Evolutionary relationships among barley and <i>Arabidopsis</i> core circadian clock and clock-associated genes

The circadian clock regulates a multitude of plant developmental and metabolic processes. In crop species, it contributes significantly to plant performance and productivity and to the adaptation and geographical range over which crops can be grown. To understand the clock in barley and how it relates to the components in the Arabidopsis thaliana clock, we have performed a systematic analysis of core circadian clock and clock-associated genes in barley, Arabidopsis and another eight species including tomato, potato, a range of monocotyledonous species and the moss, Physcomitrella patens. We have identified orthologues and paralogues of Arabidopsis genes which are conserved in all species, monocot/dicot differences, species-specific differences and variation in gene copy number (e.g. gene duplications among the various species). We propose that the common ancestor of barley and Arabidopsis had two-thirds of the key clock components identified in Arabidopsis prior to the separation of the monocot/dicot groups. After this separation, multiple independent gene duplication events took place in both monocot and dicot ancestors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00239-015-9665-0) contains supplementary material, which is available to authorized users

Measurement of the production of a W boson in association with a charm quark in pp collisions at √s = 7 TeV with the ATLAS detector

The production of a W boson in association with a single charm quark is studied using 4.6 fb−1 of pp collision data at s√ = 7 TeV collected with the ATLAS detector at the Large Hadron Collider. In events in which a W boson decays to an electron or muon, the charm quark is tagged either by its semileptonic decay to a muon or by the presence of a charmed meson. The integrated and differential cross sections as a function of the pseudorapidity of the lepton from the W-boson decay are measured. Results are compared to the predictions of next-to-leading-order QCD calculations obtained from various parton distribution function parameterisations. The ratio of the strange-to-down sea-quark distributions is determined to be 0.96+0.26−0.30 at Q 2 = 1.9 GeV2, which supports the hypothesis of an SU(3)-symmetric composition of the light-quark sea. Additionally, the cross-section ratio σ(W + +c¯¯)/σ(W − + c) is compared to the predictions obtained using parton distribution function parameterisations with different assumptions about the s−s¯¯¯ quark asymmetry

Structural Basis for Substrate Specificity in Human Monomeric Carbonyl Reductases

Carbonyl reduction constitutes a phase I reaction for many xenobiotics and is carried out in mammals mainly by members of two protein families, namely aldo-keto reductases and short-chain dehydrogenases/reductases. In addition to their capacity to reduce xenobiotics, several of the enzymes act on endogenous compounds such as steroids or eicosanoids. One of the major carbonyl reducing enzymes found in humans is carbonyl reductase 1 (CBR1) with a very broad substrate spectrum. A paralog, carbonyl reductase 3 (CBR3) has about 70% sequence identity and has not been sufficiently characterized to date. Screening of a focused xenobiotic compound library revealed that CBR3 has narrower substrate specificity and acts on several orthoquinones, as well as isatin or the anticancer drug oracin. To further investigate structure-activity relationships between these enzymes we crystallized CBR3, performed substrate docking, site-directed mutagenesis and compared its kinetic features to CBR1. Despite high sequence similarities, the active sites differ in shape and surface properties. The data reveal that the differences in substrate specificity are largely due to a short segment of a substrate binding loop comprising critical residues Trp229/Pro230, Ala235/Asp236 as well as part of the active site formed by Met141/Gln142 in CBR1 and CBR3, respectively. The data suggest a minor role in xenobiotic metabolism for CBR3. ENHANCED VERSION: This article can also be viewed as an enhanced version in which the text of the article is integrated with interactive 3D representations and animated transitions. Please note that a web plugin is required to access this enhanced functionality. Instructions for the installation and use of the web plugin are available in Text S1