A Survey of the Insects of White Sands National Monument, Tularosa
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The Proteome Map of the Escamolera
This is the Post-print version of the following article: José A. Huerta-Ocampo, María S. García-Muñoz, Aída J. Velarde-Salcedo, Eric E. Hernández- Domínguez, Jorge L. González-Escobar, Alberto Barrera-Pacheco, Alicia Grajales-Lagunes, Ana P. Barba de la Rosa, The proteome map of the escamolera ant (Liometopum apiculatum Mayr) larvae reveals immunogenic proteins and several hexamerin proteoforms, Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, Volume 28, 2018, Pages 107- 121, Pages 8-18, which has been published in final form at: https://doi.org/10.1016/j.cbd.2018.07.004 © 2018. This manuscript version is made available under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license http://creativecommons.org/licenses/by-nc-nd/4.0/ Accepted Manuscript The proteome map of the escamolera ant (Liometopum apiculatum Mayr) larvae reveals immunogenic proteins and several hexamerin proteoforms José A. Huerta-Ocampo, María S. García-Muñoz, Aida J. Velarde- Salcedo, Eric E. Hernández-Domínguez, Jorge L. González- Escobar, Alberto Barrera-Pacheco, Alicia Grajales-Lagunes, Ana P. Barba de la Rosa PII: S1744-117X(18)30052-2 DOI: doi:10.1016/j.cbd.2018.07.004 Reference: CBD 514 Comparative Biochemistry and Physiology - Part D: Genomics and To appear in: Proteomics Received 22 January 2018 date: Revised 20 July 2018 date: Accepted 20 July 2018 date: Please cite this article as: José A. Huerta-Ocampo, María S. García-Muñoz, Aida J. Velarde-Salcedo, Eric E. Hernández-Domínguez, Jorge L. González-Escobar, Alberto Barrera-Pacheco, Alicia Grajales-Lagunes, Ana P. Barba de la Rosa , The proteome map of the escamolera ant (Liometopum apiculatum Mayr) larvae reveals immunogenic proteins and several hexamerin proteoforms. -
Invertebrate Distribution and Diversity Assessment at the U. S. Army Pinon Canyon Maneuver Site a Report to the U
Invertebrate Distribution and Diversity Assessment at the U. S. Army Pinon Canyon Maneuver Site A report to the U. S. Army and U. S. Fish and Wildlife Service G. J. Michels, Jr., J. L. Newton, H. L. Lindon, and J. A. Brazille Texas AgriLife Research 2301 Experiment Station Road Bushland, TX 79012 2008 Report Introductory Notes The invertebrate survey in 2008 presented an interesting challenge. Extremely dry conditions prevailed throughout most of the adult activity period for the invertebrates and grass fires occurred several times throughout the summer. By visual assessment, plant resources were scarce compared to last year, with few green plants and almost no flowering plants. Eight habitats and nine sites continued to be sampled in 2008. The Ponderosa pine/ yellow indiangrass site was removed from the study after the low numbers of species and individuals collected there in 2007. All other sites from the 2007 survey were included in the 2008 survey. We also discontinued the collection of Coccinellidae in the 2008 survey, as only 98 individuals from four species were collected in 2007. Pitfall and malaise trapping were continued in the same way as the 2007 survey. Sweep net sampling was discontinued to allow time for Asilidae and Orthoptera timed surveys consisting of direct collection of individuals with a net. These surveys were conducted in the same way as the time constrained butterfly (Papilionidea and Hesperoidea) surveys, with 15-minute intervals for each taxanomic group. This was sucessful when individuals were present, but the dry summer made it difficult to assess the utility of these techniques because of overall low abundance of insects. -
Functional Response and Predation Potential of Hyperaspis Campestris
January - February 2020 ISSN: 0193 - 4120 Page No. 5976 - 5985 Functional Response and Predation Potential of Hyperaspis Campestris (Herbst 1783) (Coleoptera: Coccinellidae) on Opuntiae Cochineal Dactylopius Opuntiae (Hemiptera: Dactylopiidae) in Morocco Mohamed El Aalaoui,1,4*, Rachid Bouharroud,1 Mohamed Sbaghi,2 Mustapha El Bouhssini,3 and Lahoucine Hilali,4 1Integrated Crop Production Unit, Regional Center of Agadir, National Institute of Agronomic Research, Morocco. Emails: [email protected] (Corresponding author) and [email protected], 2National Institute of Agronomic Research, Plant Protection Department, Scientific Division, Rabat Morocco. Emails: [email protected] 3 International Center for Agricultural Research in the Dry Areas (ICARDA), Rabat, Morocco. Email: [email protected] 4Faculty of Science and Technology of Settat, Morocco. Email: [email protected] *Corresponding author: [email protected], Article Info Abstract: Volume 82 Functional response of the lady beetle Hyperaspis campestris (Herbst 1783) Page Number: 5976 - 5985 to varying densities (1, 5, 10, 15, 20 and 25) of Dactylopius opuntiae Publication Issue: (Cockerell) young females (20 days old) were determined under controlled January-February 2020 conditions at 26±2°C, 60±10 % RH and 12:12 h L:D regime. The searching efficiency of H. campestris considerably decreased as prey density increased. The significant linear coefficient (P1) obtained by logistic regression had a negative indicating functional response type II. Attack rates (0.151, 0.101, 0.097, 0.122, 0.124 and 0.135) and handling times (3.848, 5.171, 5.417, 4.245, 4.356 and 3.940) for 1 to 25 density, respectively, were recorded using Holling‘s disc equation. -
Coccinellid Beetles Diversity in Agro-Climatic Zones of Bhubaneswar
Journal of Entomology and Zoology Studies 2017; 5(4): 1244-1248 E-ISSN: 2320-7078 P-ISSN: 2349-6800 Coccinellid beetles diversity in agro-climatic JEZS 2017; 5(4): 1244-1248 © 2017 JEZS zones of Bhubaneswar Received: 09-05-2017 Accepted: 10-06-2017 Sandeep Kumar Mukherjee Sandeep Kumar Mukherjee and Sushree Shailani Suman Associate Professor, Department of Entomology, OUAT, Abstract Bhubaneswar, India The current research was conducted to study the abundance and diversity of various species of Sushree Shailani Suman coccinellid beetles around the agro-climatic zone of Bhubaneswar. It revealed the presence of 10 1) Study Conducted at different species of lady bird beetles viz. E. vigintioctopunctata, B. suturalis, C. transversalis, C. Department of Entomology, undecimpunctata, C. septempunctata, C. sexmaculata, H. maindroni, A. cardoni, S. coccivora and P. OUAT, Bhubaneswar, India dissecta. All total of 1363 numbers of beetles have been collected (few visually counted) from different 2) PhD scholar, KIIT vegetation including vegetables, crop field, fruit orchards, etc. The abundance of P. dissecta species was University, Bhubaneswar, highest (344) contributing about 25.24% of the total population, followed by C. septempunctata (230, Odisha, India 16.87%), and C. transversalis (226, 16.58%). But in terms of species diversity, C. transversalis was the most diversified species among all followed by P. dissecta and E. vigintioctopunctata. The collected species of coccinellid were classified into three groups as per their sub-family viz. Epilachninae, Chilocorinae and Coccinellinae. Among them the coccinellinae sub-family included highest numbers of species (6) with maximum abundance in the area having 701 beetles contributing about 51.42% of all coccinellids collected. -
Critical Windows in Animal Development: Interactions Between Environment, Phenotype and Time
Critical Windows in Animal Development: Interactions Between Environment, Phenotype and Time Casey A. Mueller Department of Biological Sciences California State University San Marcos San Marcos, CA [email protected] Abstract Observable phenotypic traits of an animal are a result of the interaction between the genome and environment. Differences in phenotypic traits between individuals induced by the environment, an indicator of phenotypic plasticity, may have immediate and long-term consequences for individuals, populations and species. During development, animals are often most responsive or susceptible to changes in their environment, and phenotypic plasticity can be particularly prevalent. It is increasingly apparent that the way in which the environment influences an animal’s physiology may differ not just across a species’ lifetime, but also within a species’ ontogeny. Periods of development during which an animal may show greater likelihood of phenotypic changes are termed ‘critical windows’ or ‘sensitive periods’. Across animal taxa, experiments utilize exposures to particular environmental, chemical or pharmacological stressors at certain time points of development to detect and understand critical windows during development. This chapter examines the emergence of critical windows as an important physiological concept using examples from the literature that span model and non-model invertebrates and vertebrates exposed to a range of environmental conditions. This chapter also outlines considerations for the continued search for critical windows. Critical window experimental designs can range in complexity, and variables such as the timing of exposures, if a single or multiple doses of a stressor are used and when endpoints are assessed should be considered. A continued focus on critical windows will no doubt contribute to our growing knowledge of the interaction between the environment and physiology during animal development. -
Diversidad De Cantharidae, Lampyridae
Revista Mexicana de Biodiversidad 80: 675- 686, 2009 Diversidad de Cantharidae, Lampyridae, Lycidae, Phengodidae y Telegeusidae (Coleoptera: Elateroidea) en un bosque tropical caducifolio de la sierra de San Javier, Sonora, México Diversity of Cantharidae, Lampyridae, Lycidae, Phengodidae and Telegeusidae (Coleoptera: Elateroidea) in a tropical dry forest of the Sierra San Javier, Sonora, Mexico Santiago Zaragoza-Caballero1* y Enrique Ramírez-García2 1Laboratorio de Entomología, Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 70-153, 04510 México D. F., México. 2Estación de Biología Chamela, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 21, San Patricio 48980 Jalisco, México. *Correspondencia: [email protected] Resumen. Se presenta un estudio de la diversidad faunística de las familias Cantharidae, Lampyridae, Lycidae, Phengodidae y Telegeusidae (Coleoptera: Elateroidea), presentes en un bosque tropical caducifolio de la sierra de San Javier, Sonora, México, que corresponde al límite boreal de este biotopo en América. La recolección incluyó trampas de atracción luminosa y red entomológica aérea, se realizó en noviembre de 2003, febrero y abril de 2004, y de julio a octubre de ese mismo año, durante 5 días de cada mes. Comprende la época lluviosa (julio-octubre) y la temporada seca (noviembre-abril). Se capturó un total de 1 501 individuos que representan 30 especies. La familia más abundante fue Cantharidae con 696 individuos, seguida de Lycidae con 561, Lampyridae con 166, Phengodidae con 66 y Telegeusidae con 12. La más rica en especies fue Lycidae con 12, seguida de Cantharidae con 11, Lampyridae con 3, Phengodidae con 3 y Telegeusidae con 1. -
Butterflies and Moths of Llano County, Texas, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Lepidoptera Recorded for Imperial County California Compiled by Jeffrey Caldwell [email protected] 1-925-949-8696 Note
Lepidoptera Recorded for Imperial County California Compiled by Jeffrey Caldwell [email protected] 1-925-949-8696 Note: BMNA = Butterflies and Moths of North America web site MPG = Moth Photographers Group web site Most are from the Essig Museum’s California Moth Specimens Database web site Arctiidae. Tiger and Lichen Moths. Apantesis proxima (Notarctia proxima). Mexican Tiger Moth. 8181 [BMNA] Ectypia clio (clio). Clio Tiger Moth. 8249 Estigmene acrea (acrea). Salt Marsh Moth. 8131 Euchaetes zella. 8232 Autostichidae (Deoclonidae). Oegoconia novimundi. Four-spotted Yellowneck Moth. 1134 (Oegoconia quadripuncta mis-applied) Bucculatricidae. Ribbed Cocoon-maker Moths. Bucculatrix enceliae. Brittlebrush Moth. 0546 Cossidae. Goat Moths, Carpenterworm Moths, and Leopard Moths. Comadia henrici. 2679 Givira mucida. 2660 Hypopta palmata. 2656 Prionoxystus robiniae (mixtus). Carpenterworm or Locust Borer. 2693 Depressariidae. Pseudethmia protuberans. 1008 [MPG] Ethmiidae. Now assigned to Depressariidae. Ethmiinae. Ethmia timberlakei. 0984 Pseudethmia protuberans. 1008 Gelechiidae. Twirler Moths. Aristotelia adceanotha. 1726 [Sighting 1019513 BMNA] Chionodes abdominella. 2054 Chionodes dentella. 2071 Chionodes fructuaria. 2078 Chionodes kincaidella. 2086 (reared from Atriplex acanthocarpa in Texas) Chionodes oecus. 2086.2 Chionodes sistrella. 2116 Chionodes xanthophilella. 2125 Faculta inaequalis. Palo Verde Webworm. 2206 Friseria cockerelli. Mesquite Webworm. 1916 Gelechia desiliens. 1938 Isophrictis sabulella. 1701 Keiferia lycopersicella. Tomato Pinworm. 2047 Pectinophora gossypiella. Pink Bollworm. 2261 Prolita puertella. 1895 Prolita veledae. 1903 Geometridae. Inchworm Moths, Loopers, Geometers, or Measuring Worms. Archirhoe neomexicana. 7295 Chesiadodes coniferaria. 6535 Chlorochlamys appellaria. 7073 Cyclophora nanaria. Dwarf Tawny Wave. W 7140 Dichorda illustraria. 7055 Dichordophora phoenix. Phoenix Emerald. 7057 Digrammia colorata. Creosote Moth. 6381 Digrammia irrorata (rubricata). 6395 Digrammia pictipennata. 6372 Digrammia puertata. -
Butterflies and Moths of Pinal County, Arizona, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
2009 Pinon Canyon Invertebrate Survey Report
"- - 70.096 60.096 50.096 40.096 30.096 20.096 10.096 0.0% Fig. 1 Most abundant Apiformes species calculated as a proportion of the total abundance of Apiformes in the collection period. Pinon Canyon Maneuver Site, 2008. 04% 1 j 0.391> 0.2% 0.1% 0.0% Fig. 2 Least abundant Apiformes species calculated as a proportion of the total abundance of Apiformes in the collection period. Pinon Canyon Maneuver Site, 2008.7 Fig. 3 Most abundant Carabidae species calculated as a proportion of the total abundance of Carabidae in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 4 Least abundant Carabidae species calculated as a proportion of the total abundance of Carabidae in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 5 Asilidae species abundance calculated as a proportion of the total abundace of Asilidae in the collection period. Pinon Canyon Maneuver Site, 2008. 30.0% 25.0% 20.0% 15.0% 10.0% 5.0% 0.0% Fig. 6 Butterfly species abundance calculated as a proportion of the total abundance of butterflies in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 7 Most abundant Orthoptera species calculated as a proportion of the total abundance of Orthoptera in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 8 Moderately abundant Orthoptera species calculated as a proportion of the total abundance of Orthoptera in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 9 Least abundant Orthoptera species calculated as a proportion of the total abundance of Orthoptera in the collection period. -
2010 Season Summary Index NEW WOFTHE~ Zone 1: Yukon Territory
2010 Season Summary Index NEW WOFTHE~ Zone 1: Yukon Territory ........................................................................................... 3 Alaska ... ........................................ ............................................................... 3 LEPIDOPTERISTS Zone 2: British Columbia .................................................... ........................ ............ 6 Idaho .. ... ....................................... ................................................................ 6 Oregon ........ ... .... ........................ .. .. ............................................................ 10 SOCIETY Volume 53 Supplement Sl Washington ................................................................................................ 14 Zone 3: Arizona ............................................................ .................................... ...... 19 The Lepidopterists' Society is a non-profo California ............... ................................................. .............. .. ................... 2 2 educational and scientific organization. The Nevada ..................................................................... ................................ 28 object of the Society, which was formed in Zone 4: Colorado ................................ ... ............... ... ...... ......................................... 2 9 May 1947 and formally constituted in De Montana .................................................................................................... 51 cember -
Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying