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Diptera: Blephariceridae) from Western North America Amanda J
Entomology Publications Entomology 2008 A New Species of Blepharicera Macquart (Diptera: Blephariceridae) from Western North America Amanda J. Jacobson Iowa State University Gregory W. Courtney Iowa State University, [email protected] Follow this and additional works at: https://lib.dr.iastate.edu/ent_pubs Part of the Biology Commons, and the Entomology Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ ent_pubs/190. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Entomology at Iowa State University Digital Repository. It has been accepted for inclusion in Entomology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. A New Species of Blepharicera Macquart (Diptera: Blephariceridae) from Western North America Abstract During a review of the Blepharicera of western North America, we discovered a new species from several mid- sized rivers in southwestern Oregon and northwestern California. We hereby present descriptions of the larvae, pupae, and adults of B. kalmiopsis, new species. Diagnostic characters and a brief discussion of bionomics and distribution are also provided. Based on previous and ongoing studies, B. kalmiopsis clearly belongs to the B. micheneri Alexander species group and appears closely related to B. zionensis Alexander. Keywords Blepharicera, Blephariceridae, net-winged midges, new species, Nearctic Disciplines Biology | Entomology Comments This article is from Proceedings of the Entomological Society of Washington 110 (2008): 978, doi: 10.4289/ 0013-8797-110.4.978. -
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). -
Data Quality, Performance, and Uncertainty in Taxonomic Identification for Biological Assessments
J. N. Am. Benthol. Soc., 2008, 27(4):906–919 Ó 2008 by The North American Benthological Society DOI: 10.1899/07-175.1 Published online: 28 October 2008 Data quality, performance, and uncertainty in taxonomic identification for biological assessments 1 2 James B. Stribling AND Kristen L. Pavlik Tetra Tech, Inc., 400 Red Brook Blvd., Suite 200, Owings Mills, Maryland 21117-5159 USA Susan M. Holdsworth3 Office of Wetlands, Oceans, and Watersheds, US Environmental Protection Agency, 1200 Pennsylvania Ave., NW, Mail Code 4503T, Washington, DC 20460 USA Erik W. Leppo4 Tetra Tech, Inc., 400 Red Brook Blvd., Suite 200, Owings Mills, Maryland 21117-5159 USA Abstract. Taxonomic identifications are central to biological assessment; thus, documenting and reporting uncertainty associated with identifications is critical. The presumption that comparable results would be obtained, regardless of which or how many taxonomists were used to identify samples, lies at the core of any assessment. As part of a national survey of streams, 741 benthic macroinvertebrate samples were collected throughout the eastern USA, subsampled in laboratories to ;500 organisms/sample, and sent to taxonomists for identification and enumeration. Primary identifications were done by 25 taxonomists in 8 laboratories. For each laboratory, ;10% of the samples were randomly selected for quality control (QC) reidentification and sent to an independent taxonomist in a separate laboratory (total n ¼ 74), and the 2 sets of results were compared directly. The results of the sample-based comparisons were summarized as % taxonomic disagreement (PTD) and % difference in enumeration (PDE). Across the set of QC samples, mean values of PTD and PDE were ;21 and 2.6%, respectively. -
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. -
“Two-Tailed” Baetidae of Ohio January 2013
Ohio EPA Larval Key for the “two-tailed” Baetidae of Ohio January 2013 Larval Key for the “two-tailed” Baetidae of Ohio For additional keys and descriptions see: Ide (1937), Provonsha and McCafferty (1982), McCafferty and Waltz (1990), Lugo-Ortiz and McCafferty (1998), McCafferty and Waltz (1998), Wiersema (2000), McCafferty et al. (2005) and McCafferty et al. (2009). 1. Forecoxae with filamentous gill (may be very small), gills usually with dark clouding, cerci without dark band near middle, claws with a smaller second row of teeth. .............................. ............................................................................................................... Heterocloeon (H.) sp. (Two species, H. curiosum (McDunnough) and H. frivolum (McDunnough), are reported from Ohio, however, the larger hind wing pads used by Morihara and McCafferty (1979) to distinguish H. frivolum have not been verified by OEPA.) Figures from Ide, 1937. Figures from Müller-Liebenau, 1974. 1'. Forecoxae without filamentous gill, other characters variable. .............................................. 2 2. Cerci with alternating pale and dark bands down its entire length, body dorsoventrally flattened, gills with a dark clouded area, hind wing pads greatly reduced. ............................... ......................................................................................... Acentrella parvula (McDunnough) Figure from Ide, 1937. Figure from Wiersema, 2000. 2'. Cerci without alternating pale and dark bands, other characters variable. ............................ -
List of Animal Species with Ranks October 2017
Washington Natural Heritage Program List of Animal Species with Ranks October 2017 The following list of animals known from Washington is complete for resident and transient vertebrates and several groups of invertebrates, including odonates, branchipods, tiger beetles, butterflies, gastropods, freshwater bivalves and bumble bees. Some species from other groups are included, especially where there are conservation concerns. Among these are the Palouse giant earthworm, a few moths and some of our mayflies and grasshoppers. Currently 857 vertebrate and 1,100 invertebrate taxa are included. Conservation status, in the form of range-wide, national and state ranks are assigned to each taxon. Information on species range and distribution, number of individuals, population trends and threats is collected into a ranking form, analyzed, and used to assign ranks. Ranks are updated periodically, as new information is collected. We welcome new information for any species on our list. Common Name Scientific Name Class Global Rank State Rank State Status Federal Status Northwestern Salamander Ambystoma gracile Amphibia G5 S5 Long-toed Salamander Ambystoma macrodactylum Amphibia G5 S5 Tiger Salamander Ambystoma tigrinum Amphibia G5 S3 Ensatina Ensatina eschscholtzii Amphibia G5 S5 Dunn's Salamander Plethodon dunni Amphibia G4 S3 C Larch Mountain Salamander Plethodon larselli Amphibia G3 S3 S Van Dyke's Salamander Plethodon vandykei Amphibia G3 S3 C Western Red-backed Salamander Plethodon vehiculum Amphibia G5 S5 Rough-skinned Newt Taricha granulosa -
Check List 4(2): 92–97, 2008
Check List 4(2): 92–97, 2008. ISSN: 1809-127X NOTES ON GEOGRAPHIC DISTRIBUTION Insecta, Ephemeroptera, Baetidae: Range extensions and new state records from Kansas, U.S.A. W. Patrick McCafferty 1 Luke M. Jacobus 2 1 Department of Entomology, Purdue University. West Lafayette, Indiana 47907 USA. E-mail: [email protected] 2 Department of Biology, Indiana University. Bloomington, Indiana 47405 USA. The mayfly (Ephemeroptera) fauna of the U.S.A. other central lowland prairie states as well state of Kansas is relatively poorly documented (McCafferty et al. 2001; 2003; Guenther and (McCafferty 2001). With respect to small minnow McCafferty 2005). Some additionally common mayflies (family Baetidae), only 16 species have species will be evident from the new data we been documented with published records from present herein. Kansas. Those involve Acentrella turbida (McDunnough, 1924); Acerpenna pygmaea Our examination of additional unidentified (Hagen, 1861); Apobaetis Etowah (Traver, 1935); material of Kansas Baetidae housed in the Snow A. lakota McCafferty, 2000; Baetis flavistriga Museum, University of Kansas, Lawrence, McDunnough, 1921; B. intercalaris McDunnough, Kansas, and collected mainly by the State 1921; Callibaetis fluctuans (Walsh, 1862); C. Biological Survey of Kansas, has led to the pictus Eaton, 1871; Centroptilum album discovery of 19 additional species of Baetidae in McDunnough, 1926; C. bifurcatum McDunnough, Kansas, resulting in a new total of 35 species of 1924; Fallceon quilleri (Dodds, 1923); Baetidae now known from the state. The records Paracloeodes minutus (Daggy, 1945); P. given alphabetically below also represent the first dardanum (McDunnough, 1923); P. ephippiatum Kansas records of the genera Camelobaetidius, (Traver, 1935); P. -
Dytiscid Water Beetles (Coleoptera: Dytiscidae) of the Yukon
Dytiscid water beetles of the Yukon FRONTISPIECE. Neoscutopterus horni (Crotch), a large, black species of dytiscid beetle that is common in sphagnum bog pools throughout the Yukon Territory. 491 Dytiscid Water Beetles (Coleoptera: Dytiscidae) of the Yukon DAVID J. LARSON Department of Biology, Memorial University of Newfoundland St. John’s, Newfoundland, Canada A1B 3X9 Abstract. One hundred and thirteen species of Dytiscidae (Coleoptera) are recorded from the Yukon Territory. The Yukon distribution, total geographical range and habitat of each of these species is described and multi-species patterns are summarized in tabular form. Several different range patterns are recognized with most species being Holarctic or transcontinental Nearctic boreal (73%) in lentic habitats. Other major range patterns are Arctic (20 species) and Cordilleran (12 species), while a few species are considered to have Grassland (7), Deciduous forest (2) or Southern (5) distributions. Sixteen species have a Beringian and glaciated western Nearctic distribution, i.e. the only Nearctic Wisconsinan refugial area encompassed by their present range is the Alaskan/Central Yukon refugium; 5 of these species are closely confined to this area while 11 have wide ranges that extend in the arctic and/or boreal zones east to Hudson Bay. Résumé. Les dytiques (Coleoptera: Dytiscidae) du Yukon. Cent treize espèces de dytiques (Coleoptera: Dytiscidae) sont connues au Yukon. Leur répartition au Yukon, leur répartition globale et leur habitat sont décrits et un tableau résume les regroupements d’espèces. La répartition permet de reconnaître plusieurs éléments: la majorité des espèces sont holarctiques ou transcontinentales-néarctiques-boréales (73%) dans des habitats lénitiques. Vingt espèces sont arctiques, 12 sont cordillériennes, alors qu’un petit nombre sont de la prairie herbeuse (7), ou de la forêt décidue (2), ou sont australes (5). -
Ecography ECOG-02578 Pinkert, S., Brandl, R
Ecography ECOG-02578 Pinkert, S., Brandl, R. and Zeuss, D. 2016. Colour lightness of dragonfly assemblages across North America and Europe. – Ecography doi: 10.1111/ecog.02578 Supplementary material Appendix 1 Figures A1–A12, Table A1 and A2 1 Figure A1. Scatterplots between female and male colour lightness of 44 North American (Needham et al. 2000) and 19 European (Askew 1988) dragonfly species. Note that colour lightness of females and males is highly correlated. 2 Figure A2. Correlation of the average colour lightness of European dragonfly species illustrated in both Askew (1988) and Dijkstra and Lewington (2006). Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Note that the extracted colour values of dorsal dragonfly drawings from both sources are highly correlated. 3 Figure A3. Frequency distribution of the average colour lightness of 152 North American and 74 European dragonfly species. Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Rugs at the abscissa indicate the value of each species. Note that colour values are from different sources (North America: Needham et al. 2000, Europe: Askew 1988), and hence absolute values are not directly comparable. 4 Figure A4. Scatterplots of single ordinary least-squares regressions between average colour lightness of 8,127 North American dragonfly assemblages and mean temperature of the warmest quarter. Red dots represent assemblages that were excluded from the analysis because they contained less than five species. Note that those assemblages that were excluded scatter more than those with more than five species (c.f. the coefficients of determination) due to the inherent effect of very low sampling sizes. -
Coleoptera) Rolf G
ARTICLE IN PRESS Organisms, Diversity & Evolution 7 (2008) 255–269 www.elsevier.de/ode A genus-level supertree of Adephaga (Coleoptera) Rolf G. Beutela,Ã, Ignacio Riberab, Olaf R.P. Bininda-Emondsa aInstitut fu¨r Spezielle Zoologie und Evolutionsbiologie, FSU Jena, Germany bMuseo Nacional de Ciencias Naturales, Madrid, Spain Received 14 October 2005; accepted 17 May 2006 Abstract A supertree for Adephaga was reconstructed based on 43 independent source trees – including cladograms based on Hennigian and numerical cladistic analyses of morphological and molecular data – and on a backbone taxonomy. To overcome problems associated with both the size of the group and the comparative paucity of available information, our analysis was made at the genus level (requiring synonymizing taxa at different levels across the trees) and used Safe Taxonomic Reduction to remove especially poorly known species. The final supertree contained 401 genera, making it the most comprehensive phylogenetic estimate yet published for the group. Interrelationships among the families are well resolved. Gyrinidae constitute the basal sister group, Haliplidae appear as the sister taxon of Geadephaga+ Dytiscoidea, Noteridae are the sister group of the remaining Dytiscoidea, Amphizoidae and Aspidytidae are sister groups, and Hygrobiidae forms a clade with Dytiscidae. Resolution within the species-rich Dytiscidae is generally high, but some relations remain unclear. Trachypachidae are the sister group of Carabidae (including Rhysodidae), in contrast to a proposed sister-group relationship between Trachypachidae and Dytiscoidea. Carabidae are only monophyletic with the inclusion of a non-monophyletic Rhysodidae, but resolution within this megadiverse group is generally low. Non-monophyly of Rhysodidae is extremely unlikely from a morphological point of view, and this group remains the greatest enigma in adephagan systematics. -
Ohio EPA Macroinvertebrate Taxonomic Level December 2019 1 Table 1. Current Taxonomic Keys and the Level of Taxonomy Routinely U
Ohio EPA Macroinvertebrate Taxonomic Level December 2019 Table 1. Current taxonomic keys and the level of taxonomy routinely used by the Ohio EPA in streams and rivers for various macroinvertebrate taxonomic classifications. Genera that are reasonably considered to be monotypic in Ohio are also listed. Taxon Subtaxon Taxonomic Level Taxonomic Key(ies) Species Pennak 1989, Thorp & Rogers 2016 Porifera If no gemmules are present identify to family (Spongillidae). Genus Thorp & Rogers 2016 Cnidaria monotypic genera: Cordylophora caspia and Craspedacusta sowerbii Platyhelminthes Class (Turbellaria) Thorp & Rogers 2016 Nemertea Phylum (Nemertea) Thorp & Rogers 2016 Phylum (Nematomorpha) Thorp & Rogers 2016 Nematomorpha Paragordius varius monotypic genus Thorp & Rogers 2016 Genus Thorp & Rogers 2016 Ectoprocta monotypic genera: Cristatella mucedo, Hyalinella punctata, Lophopodella carteri, Paludicella articulata, Pectinatella magnifica, Pottsiella erecta Entoprocta Urnatella gracilis monotypic genus Thorp & Rogers 2016 Polychaeta Class (Polychaeta) Thorp & Rogers 2016 Annelida Oligochaeta Subclass (Oligochaeta) Thorp & Rogers 2016 Hirudinida Species Klemm 1982, Klemm et al. 2015 Anostraca Species Thorp & Rogers 2016 Species (Lynceus Laevicaudata Thorp & Rogers 2016 brachyurus) Spinicaudata Genus Thorp & Rogers 2016 Williams 1972, Thorp & Rogers Isopoda Genus 2016 Holsinger 1972, Thorp & Rogers Amphipoda Genus 2016 Gammaridae: Gammarus Species Holsinger 1972 Crustacea monotypic genera: Apocorophium lacustre, Echinogammarus ischnus, Synurella dentata Species (Taphromysis Mysida Thorp & Rogers 2016 louisianae) Crocker & Barr 1968; Jezerinac 1993, 1995; Jezerinac & Thoma 1984; Taylor 2000; Thoma et al. Cambaridae Species 2005; Thoma & Stocker 2009; Crandall & De Grave 2017; Glon et al. 2018 Species (Palaemon Pennak 1989, Palaemonidae kadiakensis) Thorp & Rogers 2016 1 Ohio EPA Macroinvertebrate Taxonomic Level December 2019 Taxon Subtaxon Taxonomic Level Taxonomic Key(ies) Informal grouping of the Arachnida Hydrachnidia Smith 2001 water mites Genus Morse et al. -
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).