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IDF-Report 62 (2013)
International Dragonfly Fund - Report Journal of the International Dragonfly Fund ISSN 1435-3393 Content Garrison, Rosser & Natalia von Ellenrieder A contribution to the study of the biodiversity of Odonata in Costa Rica with an emphasis on the genus Argia (Insecta: Odonata: Coenagrionidae) 1-23 Volume 62 2013 The International Dragonfly Fund (IDF) is a scientific society founded in 1996 for the improvement of odonatological knowledge and the protection of species. Internet: http://www.dragonflyfund.org/ This series intends to publish studies promoted by IDF and to facilitate cost-efficient and rapid dis- semination of odonatological data. Editorial Work: Martin Schorr Layout: Martin Schorr Indexed by Zoological Record, Thomson Reuters, UK Home page of IDF: Holger Hunger Printing: ikt Trier, Germany Impressum: International Dragonfly Fund - Report - Volume 62 Date of publication: 21.10.2013 Publisher: International Dragonfly Fund e.V., Schulstr. 7B, 54314 Zerf, Germany. E-mail: [email protected] Responsible editor: Martin Schorr International Dragonfly Fund - Report 62 (2013): 1-23 1 A contribution to the study of the biodiversity of Odonata in Costa Rica with an emphasis on the genus Argia (Insecta: Odonata: Coenagrionidae) Rosser W. Garrison1 & Natalia von Ellenrieder2 Plant Pest Diagnostics Branch, California Department of Food & Agriculture, 3294 Meadowview Road, Sacramento, CA 95832-1448, U.S.A. [email protected], [email protected] Pairs of Argia cupraurea in tandem perching along sunny river margins in Limón province. Abstract A two week trip to Costa Rica was conducted between 26 May and 8 June 2013, sampling odonates in several provinces along the center to the pacific southern por- tion of the country. -
Wq-Rule4-12Kk L.7
L.7. Calculation of Minnesota Macroinvertebrate IBIs- Draft January 26, 2017 Introduction The Index of Biotic Integrity (IBI) is one of the primary tools used by the Minnesota Pollution Control Agency (MPCA) to determine if streams are meeting their aquatic life use goals. Calculation of an IBI involves the synthesis of macroinvertebrate community information into a numerical expression of stream health. In order to apply the MPCA Macroinvertebrate IBI (MIBI) to a macroinvertebrate dataset, it is essential that all data is collected using MPCA field and laboratory protocols (MPCA 2004, MPCA 2015). This document details the process for calculating the Minnesota MIBIs from raw macroinvertebrate samples. Summary of MIBI development To account for natural differences in macroinvertebrates communities in Minnesota, streams are assigned to different stream types. These stream types use different MIBI models and biocriteria to determine the condition of the macroinvertebrate assemblage and their attainment or nonattainment of the aqutic life beneficial use. The MPCA stratified Minnesota streams into nine macroinvertebrate stream types based on the expected natural composition of stream macroinvertebrates (Table 1). Stream type is differentiated by drainage area, geographic region, thermal regime, and gradient. These stream types are used to determine thresholds (i.e., biocriteria) that interpret the calculated MIBI as meeting or exceeding the aquatic life use goal. MIBIs were developed from five individual invertebrate stream groups, with large rivers, wadable high gradient and wabable low gradient stream types each being combined for the purposes of metric testing and evaluation. A complete description of the development of MIBIs can be found in MPCA (2014). -
(Insecta: Odonata: Coenagrionidae) Including A
Revista Mexicana de Biodiversidad Revista Mexicana de Biodiversidad 89 (2018): 921 - 926 Conservation Estimating distribution area in six Argia damselflies (Insecta: Odonata: Coenagrionidae) including A. garrisoni, a threatened species Estimando el área de distribución de seis caballitos del diablo del género Argia (Insecta: Odonata: Coenagrionidae) incluyendo A. garrisoni, una especie amenazada Laura Rangel-Sánchez a, Angela Nava-Bolaños b, *, Fredy Palacino-Rodríguez a, c, Alex Córdoba-Aguilar b, a Grupo de Investigación en Odonatos de Colombia-Grupo de Investigación en Biología, Departamento de Biología, Universidad El Bosque, Av. Cra 9 No. 131A-02 Bogotá, Colombia b Departamento de Ecología Evolutiva, Instituto de Ecología, Universidad Nacional Autónoma de México, Apartado postal 70-275, Circuito Exterior, Ciudad Universitaria, 04510 Coyoacán, México City, Mexico c Centro de Investigación en Acarología, Calle 152B # 55-45, Bogotá, Colombia * Corresponding author: [email protected] (A. Nava-Bolaños) Received: 17 September 2017; accepted: 7 March 2018 Abstract Damselflies and dragonflies (Insecta: Odonata) are currently facing a number of threats. One tool to provide a straightforward assessment of risk is distribution area. Here we have used ecological niche modeling to estimate distribution range for 6 species of Argia damselflies distributed in North America: A. cuprea, A. funcki, A. garrisoni, A. harknessi, A. munda, and A. rhoadsi. These species are not included in the International Union for the Conservation of Nature (IUCN) Red List, except for A. garrisoni which has been categorized as Least Concern. Our results indicated large distribution areas for all species, except for A. garrisoni, (8,038 km2 after a refinement analysis looking for suitable habitat). -
Insect Orders V: Panorpida & Hymenoptera
Insect Orders V: Panorpida & Hymenoptera • The Panorpida contain 5 orders: the Mecoptera, Siphonaptera, Diptera, Trichoptera and Lepidoptera. • Available evidence clearly indicates that the Lepidoptera and the Trichoptera are sister groups. • The Siphonaptera and Mecoptera are also closely related but it is not clear whether the Siponaptera is the sister group of all of the Mecoptera or a group (Boreidae) within the Mecoptera. If the latter is true, then the Mecoptera is paraphyletic as currently defined. • The Diptera is the sister group of the Siphonaptera + Mecoptera and together make up the Mecopteroids. • The Hymenoptera does not appear to be closely related to any of the other holometabolous orders. Mecoptera (Scorpionflies, hangingflies) • Classification. 600 species worldwide, arranged into 9 families (5 in the US). A very old group, many fossils from the Permian (260 mya) onward. • Structure. Most distinctive feature is the elongated clypeus and labrum that together form a rostrum. The order gets its common name from the gential segment of the male in the family Panorpodiae, which is bulbous and often curved forward above the abdomen, like the sting of a scorpion. Larvae are caterpillar-like or grub- like. • Natural history. Scorpionflies are most common in cool, moist habitats. They get the name “hangingflies” from their habit of hanging upside down on vegetation. Larvae and adult males are mostly predators or scavengers. Adult females are usually scavengers. Larvae and adults in some groups may feed on vegetation. Larvae of most species are terrestrial and caterpillar-like in body form. Larvae of some species are aquatic. In the family Bittacidae males attract females for mating by releasing a sex pheromone and then presenting the female with a nuptial gift. -
CHIRONOMUS Newsletter on Chironomidae Research
CHIRONOMUS Newsletter on Chironomidae Research No. 25 ISSN 0172-1941 (printed) 1891-5426 (online) November 2012 CONTENTS Editorial: Inventories - What are they good for? 3 Dr. William P. Coffman: Celebrating 50 years of research on Chironomidae 4 Dear Sepp! 9 Dr. Marta Margreiter-Kownacka 14 Current Research Sharma, S. et al. Chironomidae (Diptera) in the Himalayan Lakes - A study of sub- fossil assemblages in the sediments of two high altitude lakes from Nepal 15 Krosch, M. et al. Non-destructive DNA extraction from Chironomidae, including fragile pupal exuviae, extends analysable collections and enhances vouchering 22 Martin, J. Kiefferulus barbitarsis (Kieffer, 1911) and Kiefferulus tainanus (Kieffer, 1912) are distinct species 28 Short Communications An easy to make and simple designed rearing apparatus for Chironomidae 33 Some proposed emendations to larval morphology terminology 35 Chironomids in Quaternary permafrost deposits in the Siberian Arctic 39 New books, resources and announcements 43 Finnish Chironomidae 47 Chironomini indet. (Paratendipes?) from La Selva Biological Station, Costa Rica. Photo by Carlos de la Rosa. CHIRONOMUS Newsletter on Chironomidae Research Editors Torbjørn EKREM, Museum of Natural History and Archaeology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway Peter H. LANGTON, 16, Irish Society Court, Coleraine, Co. Londonderry, Northern Ireland BT52 1GX The CHIRONOMUS Newsletter on Chironomidae Research is devoted to all aspects of chironomid research and aims to be an updated news bulletin for the Chironomidae research community. The newsletter is published yearly in October/November, is open access, and can be downloaded free from this website: http:// www.ntnu.no/ojs/index.php/chironomus. Publisher is the Museum of Natural History and Archaeology at the Norwegian University of Science and Technology in Trondheim, Norway. -
Chironominae 8.1
CHIRONOMINAE 8.1 SUBFAMILY CHIRONOMINAE 8 DIAGNOSIS: Antennae 4-8 segmented, rarely reduced. Labrum with S I simple, palmate or plumose; S II simple, apically fringed or plumose; S III simple; S IV normal or sometimes on pedicel. Labral lamellae usually well developed, but reduced or absent in some taxa. Mentum usually with 8-16 well sclerotized teeth; sometimes central teeth or entire mentum pale or poorly sclerotized; rarely teeth fewer than 8 or modified as seta-like projections. Ventromental plates well developed and usually striate, but striae reduced or vestigial in some taxa; beard absent. Prementum without dense brushes of setae. Body usually with anterior and posterior parapods and procerci well developed; setal fringe not present, but sometimes with bifurcate pectinate setae. Penultimate segment sometimes with 1-2 pairs of ventral tubules; antepenultimate segment sometimes with lateral tubules. Anal tubules usually present, reduced in brackish water and marine taxa. NOTESTES: Usually the most abundant subfamily (in terms of individuals and taxa) found on the Coastal Plain of the Southeast. Found in fresh, brackish and salt water (at least one truly marine genus). Most larvae build silken tubes in or on substrate; some mine in plants, dead wood or sediments; some are free- living; some build transportable cases. Many larvae feed by spinning silk catch-nets, allowing them to fill with detritus, etc., and then ingesting the net; some taxa are grazers; some are predacious. Larvae of several taxa (especially Chironomus) have haemoglobin that gives them a red color and the ability to live in low oxygen conditions. With only one exception (Skutzia), at the generic level the larvae of all described (as adults) southeastern Chironominae are known. -
Biological Monitoring of Surface Waters in New York State, 2019
NYSDEC SOP #208-19 Title: Stream Biomonitoring Rev: 1.2 Date: 03/29/19 Page 1 of 188 New York State Department of Environmental Conservation Division of Water Standard Operating Procedure: Biological Monitoring of Surface Waters in New York State March 2019 Note: Division of Water (DOW) SOP revisions from year 2016 forward will only capture the current year parties involved with drafting/revising/approving the SOP on the cover page. The dated signatures of those parties will be captured here as well. The historical log of all SOP updates and revisions (past & present) will immediately follow the cover page. NYSDEC SOP 208-19 Stream Biomonitoring Rev. 1.2 Date: 03/29/2019 Page 3 of 188 SOP #208 Update Log 1 Prepared/ Revision Revised by Approved by Number Date Summary of Changes DOW Staff Rose Ann Garry 7/25/2007 Alexander J. Smith Rose Ann Garry 11/25/2009 Alexander J. Smith Jason Fagel 1.0 3/29/2012 Alexander J. Smith Jason Fagel 2.0 4/18/2014 • Definition of a reference site clarified (Sect. 8.2.3) • WAVE results added as a factor Alexander J. Smith Jason Fagel 3.0 4/1/2016 in site selection (Sect. 8.2.2 & 8.2.6) • HMA details added (Sect. 8.10) • Nonsubstantive changes 2 • Disinfection procedures (Sect. 8) • Headwater (Sect. 9.4.1 & 10.2.7) assessment methods added • Benthic multiplate method added (Sect, 9.4.3) Brian Duffy Rose Ann Garry 1.0 5/01/2018 • Lake (Sect. 9.4.5 & Sect. 10.) assessment methods added • Detail on biological impairment sampling (Sect. -
Checklist of the Family Chironomidae (Diptera) of Finland
A peer-reviewed open-access journal ZooKeys 441: 63–90 (2014)Checklist of the family Chironomidae (Diptera) of Finland 63 doi: 10.3897/zookeys.441.7461 CHECKLIST www.zookeys.org Launched to accelerate biodiversity research Checklist of the family Chironomidae (Diptera) of Finland Lauri Paasivirta1 1 Ruuhikoskenkatu 17 B 5, FI-24240 Salo, Finland Corresponding author: Lauri Paasivirta ([email protected]) Academic editor: J. Kahanpää | Received 10 March 2014 | Accepted 26 August 2014 | Published 19 September 2014 http://zoobank.org/F3343ED1-AE2C-43B4-9BA1-029B5EC32763 Citation: Paasivirta L (2014) Checklist of the family Chironomidae (Diptera) of Finland. In: Kahanpää J, Salmela J (Eds) Checklist of the Diptera of Finland. ZooKeys 441: 63–90. doi: 10.3897/zookeys.441.7461 Abstract A checklist of the family Chironomidae (Diptera) recorded from Finland is presented. Keywords Finland, Chironomidae, species list, biodiversity, faunistics Introduction There are supposedly at least 15 000 species of chironomid midges in the world (Armitage et al. 1995, but see Pape et al. 2011) making it the largest family among the aquatic insects. The European chironomid fauna consists of 1262 species (Sæther and Spies 2013). In Finland, 780 species can be found, of which 37 are still undescribed (Paasivirta 2012). The species checklist written by B. Lindeberg on 23.10.1979 (Hackman 1980) included 409 chironomid species. Twenty of those species have been removed from the checklist due to various reasons. The total number of species increased in the 1980s to 570, mainly due to the identification work by me and J. Tuiskunen (Bergman and Jansson 1983, Tuiskunen and Lindeberg 1986). -
Huchard Et Al., 2006 1.Pdf
Acetylcholinesterase genes within the Diptera: takeover and loss in true flies Elise Huchard, Michel Martinez, Haoues Alout, Emmanuel Douzery, Georges Lutfalla, Arnaud Berthomieu, Claire Berticat, Michel Raymond, Mylene Weill To cite this version: Elise Huchard, Michel Martinez, Haoues Alout, Emmanuel Douzery, Georges Lutfalla, et al.. Acetyl- cholinesterase genes within the Diptera: takeover and loss in true flies. Proceedings of the Royal Society B: Biological Sciences, Royal Society, The, 2006, 273 (1601), pp.2595-2604. 10.1098/rspb.2006.3621. hal-01945529 HAL Id: hal-01945529 https://hal.archives-ouvertes.fr/hal-01945529 Submitted on 29 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Proc. R. Soc. B (2006) 273, 2595–2604 doi:10.1098/rspb.2006.3621 Published online 18 July 2006 Acetylcholinesterase genes within the Diptera: takeover and loss in true flies Elise Huchard1, Michel Martinez2, Haoues Alout1, Emmanuel J. P. Douzery1, Georges Lutfalla3, Arnaud Berthomieu1, Claire Berticat1, Michel Raymond1,* and Myle`ne Weill1 1Institut des Sciences -
The Semiaquatic Hemiptera of Minnesota (Hemiptera: Heteroptera) Donald V
The Semiaquatic Hemiptera of Minnesota (Hemiptera: Heteroptera) Donald V. Bennett Edwin F. Cook Technical Bulletin 332-1981 Agricultural Experiment Station University of Minnesota St. Paul, Minnesota 55108 CONTENTS PAGE Introduction ...................................3 Key to Adults of Nearctic Families of Semiaquatic Hemiptera ................... 6 Family Saldidae-Shore Bugs ............... 7 Family Mesoveliidae-Water Treaders .......18 Family Hebridae-Velvet Water Bugs .......20 Family Hydrometridae-Marsh Treaders, Water Measurers ...22 Family Veliidae-Small Water striders, Rime bugs ................24 Family Gerridae-Water striders, Pond skaters, Wherry men .....29 Family Ochteridae-Velvety Shore Bugs ....35 Family Gelastocoridae-Toad Bugs ..........36 Literature Cited ..............................37 Figures ......................................44 Maps .........................................55 Index to Scientific Names ....................59 Acknowledgement Sincere appreciation is expressed to the following individuals: R. T. Schuh, for being extremely helpful in reviewing the section on Saldidae, lending specimens, and allowing use of his illustrations of Saldidae; C. L. Smith for reading the section on Veliidae, checking identifications, and advising on problems in the taxon omy ofthe Veliidae; D. M. Calabrese, for reviewing the section on the Gerridae and making helpful sugges tions; J. T. Polhemus, for advising on taxonomic prob lems and checking identifications for several families; C. W. Schaefer, for providing advice and editorial com ment; Y. A. Popov, for sending a copy ofhis book on the Nepomorpha; and M. C. Parsons, for supplying its English translation. The University of Minnesota, including the Agricultural Experi ment Station, is committed to the policy that all persons shall have equal access to its programs, facilities, and employment without regard to race, creed, color, sex, national origin, or handicap. The information given in this publication is for educational purposes only. -
OCHTEROIDEA La Superfamilia Ochteroidea, Incluida En El Infraorden Nepomorpha, Comprende Las Familias Ochteridae Y Gelastocoridae
| 341 Resumen OCHTEROIDEA La superfamilia Ochteroidea, incluida en el infraorden Nepomorpha, comprende las familias Ochteridae y Gelastocoridae. Ambas familias están presentes en todas las regiones biogeográficas del mundo, aunque tienen mayor diversidad y abundancia en las regiones tropicales. Hasta el momento para la Argentina se han citado tres géneros y 10 especies de Gelastocoridae, y una especie de Ochteridae. Se actualiza el estado de conocimiento de sus características morfológicas, bio- logía e historia taxonómica. Se presentan claves para la identificación de las subfamilias de Gelastocoridae y los géneros de Ochteridae, diagnosis de los géneros, la lista de especies y su distribución geográfica en la Argentina. Abstract The superfamily Ochteroidea, included in the in- fraorder Nepomorpha, is comprised of the families Ochteridae and Gelastocoridae. Both of them are present in all biogeographic regions, although they are more abundant and diverse in the tropics. Up to now, three genera and 10 species of Gelastocoridae and a single one of Ochteridae have been recorded from Argentina. I provide an account of the state of knowledge of the morphology, biology and taxonomic history of both families. I present a key to the subfa- María Cecilia MELO milies of Gelastocoridae and genera of Ochteridae, diagnoses of all genera mentioned, and a list of the División Entomología, Museo de La Plata. CONICET. species recorded in Argentina with their geographic Paseo del Bosque, 1900 La Plata, Argentina distribution. [email protected] Introducción La superfamilia Ochteroidea (Hemiptera, Heteroptera, Nepomorpha) se encuentra conformada por las familias de “orilleros” Ochteridae y Gelastocoridae, típicas habitantes de las riberas de cuerpos de agua dulce (Hebsgaard et al., 2004). -
Phylogeny of Psephenidae (Coleoptera: Byrrhoidea) Based on Larval, Pupal and Adult Characters
Systematic Entomology (2007), 32, 502–538 DOI: 10.1111/j.1365-3113.2006.00374.x Phylogeny of Psephenidae (Coleoptera: Byrrhoidea) based on larval, pupal and adult characters CHI-FENG LEE1 , MASATAKA SATOˆ2 , WILLIAM D. SHEPARD3 and M A N F R E D A . J A¨CH4 1Institute of Biodiversity, National Cheng Kung University, Tainan 701, Taiwan, 2Dia Cuore 306, Kamegahora 3-1404, Midoriku, Nagoya, 458-0804, Japan, 3Essig Museum of Entomology, 201 Wellman Hall, University of California, Berkeley, CA 94720, U.S.A., and 4Natural History Museum, Burgring 7, A-1010 Wien, Austria Abstract. We conducted the first comprehensive phylogenetic analysis of Pse- phenidae, based on 143 morphological characters of adults, larvae and pupae and coded for 34 taxa, representing three outgroups and 31 psephenid genera, including four undescribed ones. A strict consensus tree calculated (439 steps, consistency index ¼ 0.45, retention index ¼ 0.75) from the two most-parsimonious cladograms indicated that the monophyly of the family and subfamilies is supported, with the exception of Eubriinae, which is paraphyletic when including Afroeubria. Here a new subfamily, Afroeubriinae (subfam.n.), is formally estab- lished for Afroeubria. The analysis also indicated that the ‘streamlined’ larva is a derived adaptive radiation. Here, suprageneric taxonomy and the evolution of some significant characters are discussed. Keys are provided to the subfamilies and genera of Psephenidae considering larvae, adults and pupae. Introduction type specimens and the association of adults and immature stages by rearing, five new genera were proposed for Ori- Psephenidae, the ‘water penny’ beetles, are characterized by ental taxa and a well-resolved phylogenetic tree was ob- the peculiar larval body shape (Figs 4–7).