Micropterna Lateralis (Stephens, 1837) (Trichoptera, Limnephilidae) Recorded in Iceland
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Arctic Biodiversity of Stream Macroinvertebrates Declines in Response to Latitudinal Change in the Abiotic Template
Arctic biodiversity of stream macroinvertebrates declines in response to latitudinal change in the abiotic template Joseph M. Culp1,2,5, Jennifer Lento2,6, R. Allen Curry2,7, Eric Luiker3,8, and Daryl Halliwell4,9 1Environment and Climate Change Canada and Wilfrid Laurier University, Department Biology and Department Geography and Environmental Studies, 75 University Avenue West, Waterloo, Ontario N2L3C5 Canada 2Canadian Rivers Institute, Department Biology, University of New Brunswick, 10 Bailey Drive, PO Box 4400, Fredericton, New Brunswick E3B 6E1 Canada 3Environment and Climate Change Canada, Fredericton, New Brunswick E3B 6E1 Canada 4National Hydrology Research Centre, Environment and Climate Change Canada, 11 Innovation Boulevard, Saskatoon, Saskatchewan S7N 3H5 Canada Abstract: We aimed to determine which processes drive patterns of a and b diversity in Arctic river benthic macrofauna across a broad latitudinal gradient spanning the low to high Arctic of eastern Canada (58 to 81oN). Further, we examined whether latitudinal differences in taxonomic composition resulted from species replacement with organisms better adapted to northerly conditions or from the loss of taxa unable to tolerate the harsh envi- ronments of higher latitudes. We used the bioclimatic envelope concept to provide a first approximation forecast of how climate warming may modify a and b diversity of Arctic rivers and to identify potential changes in envi- ronmental variables that will drive future assemblage structure. Benthic macroinvertebrates, environmental sup- porting variables, and geospatial catchment data were collected to assess drivers of ecological pattern. We compared a diversity (i.e., taxonomic richness) across latitudes and partitioned b diversity into components of nestedness and species turnover to assess their relative contributions to compositional differences. -
Lazare Botosaneanu ‘Naturalist’ 61 Doi: 10.3897/Subtbiol.10.4760
Subterranean Biology 10: 61-73, 2012 (2013) Lazare Botosaneanu ‘Naturalist’ 61 doi: 10.3897/subtbiol.10.4760 Lazare Botosaneanu ‘Naturalist’ 1927 – 2012 demic training shortly after the Second World War at the Faculty of Biology of the University of Bucharest, the same city where he was born and raised. At a young age he had already showed interest in Zoology. He wrote his first publication –about a new caddisfly species– at the age of 20. As Botosaneanu himself wanted to remark, the prominent Romanian zoologist and man of culture Constantin Motaş had great influence on him. A small portrait of Motaş was one of the few objects adorning his ascetic office in the Amsterdam Museum. Later on, the geneticist and evolutionary biologist Theodosius Dobzhansky and the evolutionary biologist Ernst Mayr greatly influenced his thinking. In 1956, he was appoint- ed as a senior researcher at the Institute of Speleology belonging to the Rumanian Academy of Sciences. Lazare Botosaneanu began his career as an entomologist, and in particular he studied Trichoptera. Until the end of his life he would remain studying this group of insects and most of his publications are dedicated to the Trichoptera and their environment. His colleague and friend Prof. Mar- cos Gonzalez, of University of Santiago de Compostella (Spain) recently described his contribution to Entomolo- gy in an obituary published in the Trichoptera newsletter2 Lazare Botosaneanu’s first contribution to the study of Subterranean Biology took place in 1954, when he co-authored with the Romanian carcinologist Adriana Damian-Georgescu a paper on animals discovered in the drinking water conduits of the city of Bucharest. -
The Study of the Zoobenthos of the Tsraudon River Basin (The Terek River Basin)
E3S Web of Conferences 169, 03006 (2020) https://doi.org/10.1051/e3sconf/202016903006 APEEM 2020 The study of the zoobenthos of the Tsraudon river basin (the Terek river basin) Ia E. Dzhioeva*, Susanna K. Cherchesova , Oleg A. Navatorov, and Sofia F. Lamarton North Ossetian state University named after K.L. Khetagurov, Vladikavkaz, Russia Abstract. The paper presents data on the species composition and distribution of zoobenthos in the Tsraudon river basin, obtained during the 2017-2019 research. In total, 4 classes of invertebrates (Gastropoda, Crustacea, Hydracarina, Insecta) are found in the benthic structure. The class Insecta has the greatest species diversity. All types of insects in our collections are represented by lithophilic, oligosaprobic fauna. Significant differences in the composition of the fauna of the Tsraudon river creeks and tributary streams have been identified. 7 families of the order Trichoptera are registered in streams, and 4 families in the river. It is established that the streamlets of the family Hydroptilidae do not occur in streams, the distribution boundary of the streamlets of Hydropsyche angustipennis (Hydropsychidae) is concentrated in the mountain-forest zone. The hydrological features of the studied watercourses are also revealed. 1 Introduction The biocenoses of flowing reservoirs of the North Caucasus, and especially small rivers, remain insufficiently explored today; particularly, there is no information about the systematic composition, biology and ecology of amphibiotic insects (mayflies, stoneflies, caddisflies and dipterous) of the studied basin. Amphibiotic insects are an essential link in the food chain of our reservoirs and at the same time can be attributed to reliable indicators of water quality. -
Species Fact Sheet
SPECIES FACT SHEET Common Name: Scott’s apatanian caddisfly Scientific Name: Allomyia scotti Wiggins 1973 (Imania) Synonyms: Imania scotti Phylum: Mandibulata Class: Insecta Order: Trichoptera Family: Apataniidae Genus: Allomyia Conservation Status: Global Status (2005): G1 National Status (1999): N1 State Statuses: Oregon: S1 (NatureServe 2010). Type Locality: OREGON, Clackamas and Hood River counties, Mt. Hood, 1st to 3rd order streams originating from perennial seeps and springs supplied by permanent snowfields around Mt. Hood at elevations from 3,500 to 5,700 feet (Wiggins 1973b; Wanner and Arendt 2015). Water was clear and cold, temperature in July and August between 2 and 6ºC. Rocks in the stream bear dense growths of a wiry moss (Wiggins 1973b; Wanner and Arendt 2015). Technical Description (Wiggins 1973b): Adult: Length of forewing male 7.7-8.1 mm, female 7.7-9.0 mm. General structure typical of the genus and for tripunctata group; dark brown in color, forewings covered uniformly with dark brown hairs. Venation similar in two sexes, essentially as illustrated for Imania bifosa Ross by Schmid (1955, see fig 15). Wing coupling mechanism consisting of approximately eight stout, non- clavate, bristles at base of hind wing, and line of short, stout, hooked setae along costal margin of hind wing which engage upon long hairs arising from anal margin of forewing (as illustrated for Lepania cascadia by Wiggins 1973a, see fig 21). Male and female genitalia described in Wiggins 1973b. Adult Caddisfly (NC State 2005). 1 Larva: Generally similar to other larvae in this genus, but distinguished primarily by the prominent horns on the head. -
Diversity and Ecosystem Services of Trichoptera
Review Diversity and Ecosystem Services of Trichoptera John C. Morse 1,*, Paul B. Frandsen 2,3, Wolfram Graf 4 and Jessica A. Thomas 5 1 Department of Plant & Environmental Sciences, Clemson University, E-143 Poole Agricultural Center, Clemson, SC 29634-0310, USA; [email protected] 2 Department of Plant & Wildlife Sciences, Brigham Young University, 701 E University Parkway Drive, Provo, UT 84602, USA; [email protected] 3 Data Science Lab, Smithsonian Institution, 600 Maryland Ave SW, Washington, D.C. 20024, USA 4 BOKU, Institute of Hydrobiology and Aquatic Ecology Management, University of Natural Resources and Life Sciences, Gregor Mendelstr. 33, A-1180 Vienna, Austria; [email protected] 5 Department of Biology, University of York, Wentworth Way, York Y010 5DD, UK; [email protected] * Correspondence: [email protected]; Tel.: +1-864-656-5049 Received: 2 February 2019; Accepted: 12 April 2019; Published: 1 May 2019 Abstract: The holometabolous insect order Trichoptera (caddisflies) includes more known species than all of the other primarily aquatic orders of insects combined. They are distributed unevenly; with the greatest number and density occurring in the Oriental Biogeographic Region and the smallest in the East Palearctic. Ecosystem services provided by Trichoptera are also very diverse and include their essential roles in food webs, in biological monitoring of water quality, as food for fish and other predators (many of which are of human concern), and as engineers that stabilize gravel bed sediment. They are especially important in capturing and using a wide variety of nutrients in many forms, transforming them for use by other organisms in freshwaters and surrounding riparian areas. -
Trichoptera, Apataniidae) from China
European Journal of Taxonomy 333: 1–20 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.333 www.europeanjournaloftaxonomy.eu 2017 · Xu J. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Research article urn:lsid:zoobank.org:pub:60C69946-44B4-4A85-86EF-F63D489E1E4E Associations and a new species of the genus Apatidelia (Trichoptera, Apataniidae) from China Jihua XU 1, Yue XIE 2, Beixin WANG 3 & Changhai SUN 4,* 1, 2, 3, 4 Lab of Insect Taxonomy, College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, China. * Corresponding author: [email protected] 1 Email: [email protected] 2 Email: [email protected] 3 Email: [email protected] 1 urn:lsid:zoobank.org:author:8F03EA8B-8C81-48FD-8450-CD811CB220F6 2 urn:lsid:zoobank.org:author:7E32A66C-AE20-499D-90D3-D8D5B1645303 3 urn:lsid:zoobank.org:author:50CCADCC-F66A-49B2-8BAE-B12FE6229509 4 urn:lsid:zoobank.org:author:DD6E8DE5-3E20-4F9E-BC80-5FF92CE798F1 Abstract. Nine individuals of Apatidelia from Zhejiang Province, China were examined and their barcode sequences were generated and analyzed. A new species, A. morsei Xu & Sun sp. nov., is described and illustrated. The larva, male and female of A. acuminata Leng & Yang, 1998 and the male and female of A. morsei Xu & Sun sp. nov. are associated by mtCOI gene sequences. The male of A. acuminata Leng & Yang, 1998 is re-described and re-illustrated, and the female and the larva of the same species are also described and illustrated. Females and larvae of the genus are here reported for the first time. -
The Trichoptera of North Carolina
Families and genera within Trichoptera in North Carolina Spicipalpia (closed-cocoon makers) Integripalpia (portable-case makers) RHYACOPHILIDAE .................................................60 PHRYGANEIDAE .....................................................78 Rhyacophila (Agrypnia) HYDROPTILIDAE ...................................................62 (Banksiola) Oligostomis (Agraylea) (Phryganea) Dibusa Ptilostomis Hydroptila Leucotrichia BRACHYCENTRIDAE .............................................79 Mayatrichia Brachycentrus Neotrichia Micrasema Ochrotrichia LEPIDOSTOMATIDAE ............................................81 Orthotrichia Lepidostoma Oxyethira (Theliopsyche) Palaeagapetus LIMNEPHILIDAE .....................................................81 Stactobiella (Anabolia) GLOSSOSOMATIDAE ..............................................65 (Frenesia) Agapetus Hydatophylax Culoptila Ironoquia Glossosoma (Limnephilus) Matrioptila Platycentropus Protoptila Pseudostenophylax Pycnopsyche APATANIIDAE ..........................................................85 (fixed-retreat makers) Apatania Annulipalpia (Manophylax) PHILOPOTAMIDAE .................................................67 UENOIDAE .................................................................86 Chimarra Neophylax Dolophilodes GOERIDAE .................................................................87 (Fumanta) Goera (Sisko) (Goerita) Wormaldia LEPTOCERIDAE .......................................................88 PSYCHOMYIIDAE ....................................................68 -
Aquatic Macroinvertebrate Identification with Insect Families
MiCorp Site ID#___________________ Identification verified by:_________________(optional) AQUATIC MACROINVERTEBRATE IDENTIFICATION WITH INSECT FAMILIES Use letter code [R (rare) = 1-10, C (common) = 11 or more] to record the approximate numbers of organisms in each taxa found in the stream reach. Only use the blank by the main taxa heading (i.e. ANNELIDA, COLEOPTERA) when there are organisms that cannot be identified to the lower taxonomic levels. Enter both the family level data as well as the order level data into the Michigan Data Exchange. ANNELIDA— Segmented Worm______ DIPTERA— continued Hirudinea Syrphidae Oligochaeta Tabanidae Tipulidae COLEOPTERA — Beetles___________ Chrysomelidae EPHEMEROPTERA — Mayflies____ Curculionidae Acanthametropodidae Dryopidae Ameletidae Dytiscidae Ametropodidae Elmidae Arthropleidae Gyrinidae Baetidae Haliplidae Baetiscidae Hydraenidae Caenidae Hydrophilidae Ephemerellidae Lampyridae Ephemeridae Lutrochidae Heptageniidae Noteridae Isonychiidae Psephenidae Leptohyphidae Ptilodactylidae Leptophlebiidae Scirtidae Metretopodidae Staphylinidae Neoephemeridae Oligoneuridae COLLEMBOLA — Springtail_________ Polymitarcyidae Potamanthidae CRUSTACEA— Crustaceans________ Pseudironidae Amphipoda Siphlonuridae Decapoda Tricorythidae Isopoda GASTROPODA — Snails, Limpets__ DIPTERA — True Flies______________ Ancylidae Athericidae Physidae Blephariceridae Planorbidae Ceratopogonidae Right-handed snail Chaoboridae Chironomidae HEMIPTERA — True Bugs_________ Culicidae Belostomatidae Dixidae Corixidae Dolichopodidae Gelastocoridae -
Andrew (Andy) Peebles Nimmo 9 December 1938
5 BRAUERIA (Lunz am See, Austria) 43:5-10 (2016) teaching (mostly Chemistry) in evening and summer classes in Edmonton Continuing Education and in schools throughout the Andrew (Andy) Peebles Nimmo city. He is survived by his wife of 12 years, Carita Nybom, daughters Alice (Douglas James) and Emma Nimmo, 9 December 1938 — 14 May 2015 grandchildren Gillian and Thomas Nimmo-James and is warmly remembered by his many friends and colleagues in the On May 14, 2015, with the death of Andy Nimmo, World Trichoptera community and in Edmonton and the Canada lost a prominent student of the Trichoptera. In addition University of Alberta. Andy was a long-time substitute science teacher, bibliographer, Dave Ruiter & Bruce Hemming forester, naturalist and outdoorsman (he fashioned camp fires that would have been visible from the moon with the unaided Curriculum vitae eye), philatelist (he served on the executive committee of the Edmonton Stamp Club for many years), voracious reader, world Marital: Married. 22 June 1968, to Susan Mary Hird, traveler, railway buff (he, twice [1989, 2012] crossed Russia [Discarded by her, 1999]. - Two daughters: Alice Nora, 8 July from Vladivostok to Moscow on the Trans Siberian Railway 1970, Emma Jane, 30 November 1972. - Married, 23 March and worked the summer of 1974 as a machinist’s helper in 2003, to Carita Lynn Elizabeth Nybom, of Helsinki, Finland. Canadian National’s diesel shops in the Calder yards, Edmonton), pipe-smoker (using tobacco he grew himself), and Education: Until November, 1953, I attended school in dour but proud Scot. Bom in Wick, Caithness, in the extreme Scotland, initially the Primary School in Torrance, near northeast of Scotland (his father, David McKay Nimmo, served Glasgow, followed by the West School, Kirkcaldy, Fife. -
Stomach Analysis of Top Aquatic Predators in a Headwater Stream Network
Stomach Analysis of Top Aquatic Predators in a Headwater Stream Network By Najma Binti Hashim Ain An Undergraduate Thesis Submitted to Oregon State University In partial fulfillment of the requirements for the degree of Baccalaureate of Science in BioResource Research, Sustainable Ecosystem Option June 9, 2020 Commencement June 2020 APPROVED: _____________________________________________________ ______________ Ivan Arismendi, Department of Fisheries and Wildlife June 9, 2020 ____________________________________________________ _______________ Maryam Kamran, Department of Fisheries and Wildlife June 9, 2020 _____________________________________________________ ______________ Katharine G. Field, BRR Director June 9, 2020 © Copyright by Najma Binti Hashim Ain, June 9, 2020 I understand that my project will become part of the permanent collection of the Oregon State University Library, and will become part of the Scholars Archive collection for BioResource Research. My signature below authorizes the release of my project and thesis to any reader upon request. _______________________________________________________ ____________ Najma Binti Hashim Ain 6/9/2020 STOMACH ANALYSIS OF TOP AQUATIC PREDATORS IN A HEADWATER STREAM NETWORK ABSTRACT Top predators play important roles in regulating communities and ecosystem processes in freshwater ecosystems. In the headwater stream network, it is crucial to understand the interspecific interaction between multiple predators. In Oregon forested ecosystems, Coastal Giant Salamander (Dicamptodon tenebrosus) and cutthroat trout (Oncorhynchus clarkii) are the top predators in many perennial headwater streams. Both feed on aquatic invertebrates and thus, they are potential competitors. In this study, we assessed the diet variation in headwater stream predators. The research objectives are to understand the dietary composition of both predators in different locations within the headwater stream and to compare the similitudes and differences based on their diet and body size. -
Updated Checklist of the Michigan (USA) Caddisflies, with Regional and Habitat Affinities
A peer-reviewed open-access journal ZooKeys Updated730: 57–74 checklist(2017) of the Michigan (USA) caddisflies, with regional and habitat affinities 57 doi: 10.3897/zookeys.730.21776 CHECKLIST http://zookeys.pensoft.net Launched to accelerate biodiversity research Updated checklist of the Michigan (USA) caddisflies, with regional and habitat affinities David C. Houghton1, R. Edward DeWalt2, Angelica J. Pytel1, Constance M. Brandin1, Sarah E. Rogers1, David E. Ruiter3, Ethan Bright4, Patrick L. Hudson5, Brian J. Armitage6 1 Department of Biology, Hillsdale College, 33 East College Street, Hillsdale, MI 49242, USA 2 Illinois Na- tural History Survey, 1816 South Oak Street, Champaign IL 61820, USA 3 235 SW Central Avenue, Grants Pass, OR 97526, USA 4 Museum of Zoology, University of Michigan, Ann Arbor, MI 48103, USA 5 Great Lakes Science Center, US Geological Survey, 1451 Green Road, Ann Arbor, MI 48105, USA 6 Instituto Conmemorativo Gorgas de Estudio de la Salud, Ave. Justo Arosemena y Calle 35, Apartado Postal No 0816- 02593, Ciudad de Panamá, Republic of Panamá Corresponding author: David C. Houghton ([email protected]) Academic editor: A. Previšić | Received 20 October 2017 | Accepted 6 December 2017 | Published 17 January 2018 http://zoobank.org/D8CA634C-3ED1-49E4-92E5-C91DFFB327E3 Citation: Houghton DC, DeWalt RE, Pytel AJ, Brandin CM, Rogers SE, Ruiter DE, Bright E, Hudson PL, Armitage BJ (2018) Updated checklist of the Michigan (USA) caddisflies, with regional and habitat affinities. ZooKeys 730: 57–74. https://doi.org/10.3897/zookeys.730.21776 Abstract Based on examination of ~180,000 specimens from 695 collections of 443 localities collected from the 1930s to 2015 we report 295 species of caddisflies from Michigan. -