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A New Species of Behningia Lestage, 1929 (Ephemerotera: Behningiidae) from China
Zootaxa 4671 (3): 420–426 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2019 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4671.3.7 http://zoobank.org/urn:lsid:zoobank.org:pub:EED176F4-BDA3-4053-A36C-8A76D3C4C186 A new species of Behningia Lestage, 1929 (Ephemerotera: Behningiidae) from China XIONGDONG ZHOU1, MIKE BISSET2, MENGZHEN XU3,5 & ZHAOYIN WANG4 1State Key Laboratory of Hydroscience and Engineering, Tsinghua University, Beijing, China. E-mail: [email protected] 2Department of Physics, Tsinghua University, Beiing, China. E-mail: [email protected] 3State Key Laboratory of Hydroscience and Engineering, Tsinghua University, Beijing, China. E-mail: [email protected] 4State Key Laboratory of Hydroscience and Engineering, Tsinghua University, Beijing, China. E-mail: [email protected] 5Corresponding author Abstract A new species of sand-burrowing mayfly (Ephemeroptera: Behningiidae), Behningia nujiangensis Zhou & Bisset, is described based on more than 50 nymphs collected from the Nujiang River in Yunnan Province, P.R. China. This is the first species of the family Behningiidae discovered in China. It is also the second species of genus Behningia, and the third species of the family Behningiidae collected from the Oriental biogeographic region. The shapes of the labrum and the labium in B. nujiangensis are markedly different from those found in other species of Behningia. Differences in the mandibles, the galea-lacina of maxillae, and both the prothoracic and metathoracic legs differentiate B. nujiangensis from both B. baei and B. ulmeri. The biology of and conservation challenges for B. nujiangensis are also briefly discussed. -
Forestiera Lace Bugs Leptoypha Elliptica (From Wheeler, 2002) (No Common Names) Leptoypha Elliptica Leptoypha Ilicis Contributor: Alfred G
Forestiera Lace Bugs Leptoypha elliptica (from Wheeler, 2002) (No common names) Leptoypha elliptica Leptoypha ilicis Contributor: Alfred G. Wheeler DESCRIPTION Taxonomy and Basic Description Both adults and nymphs of the family Tingidae are strictly phytophagous. Lace bugs are mostly host restricted, developing on plants of only one genus or several related genera. They are found mainly on woody plants, the nymphs feeding on lower surfaces of leaves. Their feeding on mesophyll tissues usually results in a bleached or chlorotic appearance of the upper leaf surface and dark spots of excrement on the lower surface. Some lace bugs feed on herbaceous vascular plants and species of one genus (Acalypta) feed mainly on mosses. Lace bugs associated with small trees and shrubs of the genus Forestiera (olive family; Oleaceae) include two morphologically similar species of Leptoypha. McAtee described L. elliptica from Texas in 1917; L. ilicis was described in 1919 from Georgia by Drake. Only recently was the specific name of the latter species shown to be a Leptoypha ilicis (from Wheeler, 2002) misnomer. This lace bug was named ilicis because of its assumed host association: Ilex sp. Its actual hosts are species of Forestiera, the plant mentioned in the original description having been misidentified. Forestiera species bear a superficial resemblance to certain species of Ilex (holly; family Aquifoliaceae). Leptoypha species are small (about 3 mm long or 0.12 inches), elongate or narrowly oblong, and straw yellow to reddish brown. A hood (prothoracic covering of the head) and paranota (lateral expansions of pronotum), which characterize many lace bugs, are lacking. Also absent is the translucent lacy appearance of the forewings (hemelytra) that is typical of the Tingidae; elevations of the forewings also are absent. -
Decapod Crustacean Grooming: Functional Morphology, Adaptive Value, and Phylogenetic Significance
Decapod crustacean grooming: Functional morphology, adaptive value, and phylogenetic significance N RAYMOND T.BAUER Center for Crustacean Research, University of Southwestern Louisiana, USA ABSTRACT Grooming behavior is well developed in many decapod crustaceans. Antennular grooming by the third maxillipedes is found throughout the Decapoda. Gill cleaning mechanisms are qaite variable: chelipede brushes, setiferous epipods, epipod-setobranch systems. However, microstructure of gill cleaning setae, which are equipped with digitate scale setules, is quite conservative. General body grooming, performed by serrate setal brushes on chelipedes and/or posterior pereiopods, is best developed in decapods at a natant grade of body morphology. Brachyuran crabs exhibit less body grooming and virtually no specialized body grooming structures. It is hypothesized that the fouling pressures for body grooming are more severe in natant than in replant decapods. Epizoic fouling, particularly microbial fouling, and sediment fouling have been shown r I m ans of amputation experiments to produce severe effects on olfactory hairs, gills, and i.icubated embryos within short lime periods. Grooming has been strongly suggested as an important factor in the coevolution of a rhizocephalan parasite and its anomuran host. The behavioral organization of grooming is poorly studied; the nature of stimuli promoting grooming is not understood. Grooming characters may contribute to an understanding of certain aspects of decapod phylogeny. The occurrence of specialized antennal grooming brushes in the Stenopodidea, Caridea, and Dendrobranchiata is probably not due to convergence; alternative hypotheses are proposed to explain the distribution of this grooming character. Gill cleaning and general body grooming characters support a thalassinidean origin of the Anomura; the hypothesis of brachyuran monophyly is supported by the conservative and unique gill-cleaning method of the group. -
An Annotated Checklist of Wisconsin Scarabaeoidea (Coleoptera)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida March 2002 An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera) Nadine A. Kriska University of Wisconsin-Madison, Madison, WI Daniel K. Young University of Wisconsin-Madison, Madison, WI Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Kriska, Nadine A. and Young, Daniel K., "An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera)" (2002). Insecta Mundi. 537. https://digitalcommons.unl.edu/insectamundi/537 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI, Vol. 16, No. 1-3, March-September, 2002 3 1 An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera) Nadine L. Kriska and Daniel K. Young Department of Entomology 445 Russell Labs University of Wisconsin-Madison Madison, WI 53706 Abstract. A survey of Wisconsin Scarabaeoidea (Coleoptera) conducted from literature searches, collection inventories, and three years of field work (1997-1999), yielded 177 species representing nine families, two of which, Ochodaeidae and Ceratocanthidae, represent new state family records. Fifty-six species (32% of the Wisconsin fauna) represent new state species records, having not previously been recorded from the state. Literature and collection distributional records suggest the potential for at least 33 additional species to occur in Wisconsin. Introduction however, most of Wisconsin's scarabaeoid species diversity, life histories, and distributions were vir- The superfamily Scarabaeoidea is a large, di- tually unknown. -
DNA Barcoding Distinguishes Pest Species of the Black Fly Genus <I
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 11-2013 DNA Barcoding Distinguishes Pest Species of the Black Fly Genus Cnephia (Diptera: Simuliidae) I. M. Confitti University of Toronto K. P. Pruess University of Nebraska-Lincoln A. Cywinska Ingenomics, Inc. T. O. Powers University of Nebraska-Lincoln D. C. Currie University of Toronto and Royal Ontario Museum, [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/entomologyfacpub Part of the Entomology Commons Confitti, I. M.; Pruess, K. P.; Cywinska, A.; Powers, T. O.; and Currie, D. C., "DNA Barcoding Distinguishes Pest Species of the Black Fly Genus Cnephia (Diptera: Simuliidae)" (2013). Faculty Publications: Department of Entomology. 616. http://digitalcommons.unl.edu/entomologyfacpub/616 This Article is brought to you for free and open access by the Entomology, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications: Department of Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. MOLECULAR BIOLOGY/GENOMICS DNA Barcoding Distinguishes Pest Species of the Black Fly Genus Cnephia (Diptera: Simuliidae) 1,2 3 4 5 1,2,6 I. M. CONFLITTI, K. P. PRUESS, A. CYWINSKA, T. O. POWERS, AND D. C. CURRIE J. Med. Entomol. 50(6): 1250Ð1260 (2013); DOI: http://dx.doi.org/10.1603/ME13063 ABSTRACT Accurate species identiÞcation is essential for cost-effective pest control strategies. We tested the utility of COI barcodes for identifying members of the black ßy genus Cnephia Enderlein (Diptera: Simuliidae). Our efforts focus on four Nearctic Cnephia speciesÑCnephia dacotensis (Dyar & Shannon), Cnephia eremities Shewell, Cnephia ornithophilia (Davies, Peterson & Wood), and Cnephia pecuarum (Riley)Ñthe latter two being current or potential targets of biological control programs. -
Palaemonetes Kadiakensis Rathbun: Post Embryonic Growth in the Laboratory (Decapoda, Palaemonidae)
PALAEMONETES KADIAKENSIS RATHBUN: POST EMBRYONIC GROWTH IN THE LABORATORY (DECAPODA, PALAEMONIDAE) BY JERRY H. HUBSCHMAN and JO ANN ROSE Department of Biology, Wright State University, Dayton, Ohio 45431, U.S.A. and Franz Theodore Stone Laboratory, Put In Bay, Ohio, U.S.A. INTRODUCTION The study of larval development in decapod Crustacea has become continually refined during the past decade. Historically, the descriptive phases of larval development of marine decapods has been based upon the study of series collected in the plankton. In time, a wide range of species representing a number of decapod orders have been reared from egg to metamorphosis in the laboratory. As a result of this work, much of the variation in size and form observed in the plankton material has also been demonstrable in the laboratory. Five species of Eastern U.S. Palaemonete.r have been reared successfully through metamorphosis in the laboratory. These represent three marine forms: Palaemonete.r vulgaris (Say) and P. pugio Holthuis by Broad (1957a, b) and P. intermedius Holthuis by Broad & Hubschman (1962); and two freshwater species: Palaemonete.r k.adiaken.ri.r Rath- bun by Broad & Hubschman (1960, 1963) and P. paludo.ru.r (Gibbes) by Dobkin (1963). Broad ( 1957b) has demonstrated variation in molting frequency and duration of larval life as a function of diet. It is apparent that the sequence of morpholo- gical and physiological changes leading to metamorphosis bears no direct relation- ship to molting history. Indeed, the control mechanisms involved in both larval processes are not known. In adult shrimp, the initiation of molting is mediated by eyestalk hormones. -
Proceedings of the United States National Museum
Proceedings of the United States National Museum SMITHSONIAN INSTITUTION • WASHINGTON, D.C. Volume 112 I960 Number 3431 LACE-BUG GENERA OF THE WORLD (HEMIPTERA: TINGIDAE) « By Carl J. Drake and Florence A. Ruhoff Introduction A treatise of the generic names of the family Tingidae from a global standpoint embodies problems similar to those frequently encountered in corresponding studies in other animal groups. The more im- portant criteria, including such basic desiderata as fixation of type species, synonyms, priority, and dates of technical publications implicate questions concomitant with recent trends toward the clarification and stabilization of zoological nomenclature. Zoogeography, predicated and authenticated on the generic level by the distribution of genera and species, is portrayed here by means of tables, charts, and maps of the tingifauna of the world. This visual pattern of distribution helps one to form a more vivid concept of the family and its hierarchic levels of subfamilies and genera. To a limited extent the data indicate distributional concentrations and probable centers of evolution and dispersal paths of genera. The phylogenetic relationship of genera is not discussed. The present treatise recognizes 216 genera (plus 79 synonyms, homonyms, and emendations) of the Tingidae of the world and gives 1 Research for this paper was supported In part by the National Science Foundation, grant No. 4095. 2 PROCEEDINGS OF THE NATIONAL MUSEUM vol. 112 the figure of 1,767 as the approximate number of species now recog- nized. These figures, collated with similar categories in Lethierry and Severin (1896), show that there has been an increase of many genera and hundreds of species of Tingidae during the past three- quarters of a century. -
Tingidae (Heteroptera) De Nicaragua
ISSN 1021-0296 REVISTA NICARAGUENSE DE ENTOMOLOGIA N° 113. Diciembre 2016 Tingidae (Heteroptera) de Nicaragua. Por Jean-Michel Maes & Alex Knudson. PUBLICACIÓN DEL MUSEO ENTOMOLÓGICO ASOCIACIÓN NICARAGÜENSE DE ENTOMOLOGÍA LEON - - - NICARAGUA Revista Nicaragüense de Entomología. Número 113. 2016. La Revista Nicaragüense de Entomología (ISSN 1021-0296) es una publicación reconocida en la Red de Revistas Científicas de América Latina y el Caribe, España y Portugal (Red ALyC) e indexada en los índices: Zoological Record, Entomológical Abstracts, Life Sciences Collections, Review of Medical and Veterinary Entomology and Review of Agricultural Entomology. Los artículos de esta publicación están reportados en las Páginas de Contenido de CATIE, Costa Rica y en las Páginas de Contenido de CIAT, Colombia. Todos los artículos que en ella se publican son sometidos a un sistema de doble arbitraje por especialistas en el tema. The Revista Nicaragüense de Entomología (ISSN 1021-0296) is a journal listed in the Latin-American Index of Scientific Journals. It is indexed in: Zoological Records, Entomológical, Life Sciences Collections, Review of Medical and Veterinary Entomology and Review of Agricultural Entomology. And reported in CATIE, Costa Rica and CIAT, Colombia. Two independent specialists referee all published papers. Consejo Editorial Jean Michel Maes Fernando Hernández-Baz Editor General Editor Asociado Museo Entomológico Universidad Veracruzana Nicaragua México José Clavijo Albertos Silvia A. Mazzucconi Universidad Central de Universidad de -
Caretta Caretta) As Revealed by Stable Isotopes and Satellite Telemetry
Mar Biol (2012) 159:1255–1267 DOI 10.1007/s00227-012-1906-9 ORIGINAL PAPER Distribution of foraging habitats of male loggerhead turtles (Caretta caretta) as revealed by stable isotopes and satellite telemetry Mariela Pajuelo · Karen A. Bjorndal · Kimberly J. Reich · Michael D. Arendt · Alan B. Bolten Received: 13 October 2011 / Accepted: 20 February 2012 / Published online: 7 March 2012 © Springer-Verlag 2012 Abstract Most studies on the foraging ecology of logger- Introduction head turtles (Caretta caretta) have focused on adult females and juveniles. Little is known about the foraging Knowledge of foraging ground distribution of highly patterns of adult male loggerheads. We analyzed tissues for migratory animals is critical for understanding their forag- carbon and nitrogen stable isotopes (13C and 15N) from ing behavior and habitat use. IdentiWcation of key habitats 29 adult male loggerheads tracked with satellite transmit- helps not only to characterize life history features of popu- ters from one breeding area in Florida, USA, to evaluate lations (Block et al. 2001), but also to assess the impact of their foraging habitats in the Northwest Atlantic (NWA). threats that populations may face (Hays et al. 2003). Most Our study revealed large variations in 13C and 15N and a eVorts to identify key habitats and movement patterns have correlation between both 13C and 15N and the latitude to used Xipper tags (Limpus et al. 1992), genetic markers which the loggerheads traveled after the mating season, (Bolker et al. 2007), chemical analysis (Thorrold et al. thus reXecting a geographic pattern in the isotopic signa- 2001), and electronic tagging (Block et al. -
South Carolina Department of Natural Resources
FOREWORD Abundant fish and wildlife, unbroken coastal vistas, miles of scenic rivers, swamps and mountains open to exploration, and well-tended forests and fields…these resources enhance the quality of life that makes South Carolina a place people want to call home. We know our state’s natural resources are a primary reason that individuals and businesses choose to locate here. They are drawn to the high quality natural resources that South Carolinians love and appreciate. The quality of our state’s natural resources is no accident. It is the result of hard work and sound stewardship on the part of many citizens and agencies. The 20th century brought many changes to South Carolina; some of these changes had devastating results to the land. However, people rose to the challenge of restoring our resources. Over the past several decades, deer, wood duck and wild turkey populations have been restored, striped bass populations have recovered, the bald eagle has returned and more than half a million acres of wildlife habitat has been conserved. We in South Carolina are particularly proud of our accomplishments as we prepare to celebrate, in 2006, the 100th anniversary of game and fish law enforcement and management by the state of South Carolina. Since its inception, the South Carolina Department of Natural Resources (SCDNR) has undergone several reorganizations and name changes; however, more has changed in this state than the department’s name. According to the US Census Bureau, the South Carolina’s population has almost doubled since 1950 and the majority of our citizens now live in urban areas. -
Insects That Feed on Trees and Shrubs
INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, -
Folk Taxonomy, Nomenclature, Medicinal and Other Uses, Folklore, and Nature Conservation Viktor Ulicsni1* , Ingvar Svanberg2 and Zsolt Molnár3
Ulicsni et al. Journal of Ethnobiology and Ethnomedicine (2016) 12:47 DOI 10.1186/s13002-016-0118-7 RESEARCH Open Access Folk knowledge of invertebrates in Central Europe - folk taxonomy, nomenclature, medicinal and other uses, folklore, and nature conservation Viktor Ulicsni1* , Ingvar Svanberg2 and Zsolt Molnár3 Abstract Background: There is scarce information about European folk knowledge of wild invertebrate fauna. We have documented such folk knowledge in three regions, in Romania, Slovakia and Croatia. We provide a list of folk taxa, and discuss folk biological classification and nomenclature, salient features, uses, related proverbs and sayings, and conservation. Methods: We collected data among Hungarian-speaking people practising small-scale, traditional agriculture. We studied “all” invertebrate species (species groups) potentially occurring in the vicinity of the settlements. We used photos, held semi-structured interviews, and conducted picture sorting. Results: We documented 208 invertebrate folk taxa. Many species were known which have, to our knowledge, no economic significance. 36 % of the species were known to at least half of the informants. Knowledge reliability was high, although informants were sometimes prone to exaggeration. 93 % of folk taxa had their own individual names, and 90 % of the taxa were embedded in the folk taxonomy. Twenty four species were of direct use to humans (4 medicinal, 5 consumed, 11 as bait, 2 as playthings). Completely new was the discovery that the honey stomachs of black-coloured carpenter bees (Xylocopa violacea, X. valga)were consumed. 30 taxa were associated with a proverb or used for weather forecasting, or predicting harvests. Conscious ideas about conserving invertebrates only occurred with a few taxa, but informants would generally refrain from harming firebugs (Pyrrhocoris apterus), field crickets (Gryllus campestris) and most butterflies.