Individual Development Plan Template
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Species Fact Sheet for Homoplectra Schuhi
SPECIES FACT SHEET Common Name: Schuh’s Homoplectran Caddisfly Scientific Name: Homoplectra schuhi Denning 1965 Phylum: Mandibulata Class: Insecta Order: Trichoptera Suborder: Annulipalpia Family: Hydropsychidae Subfamily: Diplectroninae Conservation Status Global Status (2005): G3Q – Vulnerable, but taxonomic questions persist (last reviewed 25 Mar 2005) National Status (United States): N3 - Vulnerable (23 Feb 2005) State Status (Oregon): S3 - Vulnerable (NatureServe 2015) Oregon Biodiversity Information Center: List 3 IUCN Red List: NE – Not evaluated Taxonomic Note This species has been given a global status of G3Q due to the limited number of specimens that have been reviewed to date, and the variability of diagnostic characteristics (NatureServe 2015). This genus is in need of additional collecting and taxonomic review, which may lead to synonymization with older described species (Wisseman 2015, Ruiter 2015). For example, specimens identified as H. luchia Denning 1966 may in fact be synonyms of H. schuhi (Ruiter 2015). Technical Description A microscope is required to identify Homoplectra schuhi, as identifications are based on genitalia anatomy. The advice of a Trichoptera expert is suggested. See Denning (1965) for lateral view drawings of the male and female genitalia. Adult: The adults of this species are small, moth-like insects in the caddisfly family Hydropsychidae. Homoplectra males are recognized by the complexity of the phallic apparatus, which can be complicated by very strong development of several sclerotized branches (Schmid 1998). Holotype male: Length 6 mm. General color of head, thorax and abdomen dark brown, wings tan with no pattern, legs and antennae varying shades of brownish. Pubescence of head, thorax and legs aureous. Fifth sternite with a dorsal filament enlarged distally and curved dorso-caudad. -
Insecta: Trichoptera) from the Ecoregion Hellenic Western Balkans
Nat. Croat. Vol. 26(2), 2017 197 NAT. CROAT. VOL. 26 No 2 197-204 ZAGREB DECEMBER 31, 2017 original scientific paper / izvorni znanstveni rad DOI 10.20302/NC.2017.26.16 FIRST RECORD OF TRIAENODES BICOLOR (CURTIS, 1834) (INSECTA: TRICHOPTERA) FROM THE ECOREGION HELLENIC WESTERN BALKANS Halil Ibrahimi1, Ruzhdi Kuçi2*, Astrit Bilalli3 & Ermira Gashi1 1Department of Biology, Faculty of Mathematical and Natural Sciences, University of Prishtina “Hasan Prishtina”, “Mother Theresa” p.n., 10 000 Prishtinë, Republic of Kosovo 2Faculty of Education, University of Prishtina “Hasan Prishtina”, “Mother Teresa” p.n., 10 000 Prishtinë, Republic of Kosovo 3Faculty of Agribusiness, University of Peja “Haxhi Zeka”, “UÇK” street, 30 000 Pejë, Republic of Kosovo Ibrahimi, H., Kuçi, R., Bilalli, A. & Gashi, E.: First record of Triaenodes bicolor (Curtis, 1834) (Insecta: Trichoptera) from the Ecoregion Hellenic Western Balkans. Nat. Croat., Vol. 26, No. 2., 197-204, Zagreb, 2017. We collected adult caddisfly specimens with entomological nets and ultraviolet light traps monthly from May to November 2012 in Brezne Lake situated in Dragash Municipality. During this investigation we found the Leptocerid species Triaenodes bicolor for the first time in Kosovo; it is also the first record for Ecoregion 6, Hellenic Western Balkans. Additionally, this is the first record of the genus Triaenodes from Kosovo. In total seven males and three females of this species were found. Triaenodes bicolor is present all over the European continent but has been rarely sampled in southeastern Europe. Other taxa sympatric with Triaenodes bicolor in the investigated locality are: Hydropsyche instabilis, Hydropsyche spp., Plectrocnemia conspersa, Plectrocnemia spp., Micropterna nycterobia, Micropterna sequax, Limnephilus vittatus, Limnephilus auricula and Thremma anomalum. -
Publications of Glenn B
Publications: Glenn B. Wiggins, Curator Emeritus, Entomology 2010 Wiggins, G.B. “No small matters. Introducing Biological Notes on an Old Farm: Exploring Common Things in the Kingdoms of Life.” ROM Magazine, 42(2): 29- 31. * 2009 Wiggins, G.B. Biological Notes on an Old Farm: Exploring Common Things in the Kingdoms of Life. Royal Ontario Museum, Toronto. 2008 Wiggins, G.B. and D.C. Currie. “Trichoptera Families.” In An Introduction to the Aquatic Insects of North America, edited by R.W. Merritt, K.W. Cummins, and M.B. Berg. Kendall/Hunt, Dubuque, Iowa (4th edition, revised). 2007 Wiggins, G.B. “Architects under water.” American Entomologist, 53(2): 78-85. 2005b Wiggins, G.B. “Review: Vernal pools, natural history and conservation by Elizabeth A. Colburn.” Journal of the North American Benthological Society, 24(4): 1009-1013. 2005a Vineyard, R.N., G.B. Wiggins, H.E. Frania, and P.W. Schefter. “The caddisfly genus Neophylax (Trichoptera: Uenoidae).” Royal Ontario Museum Contributions in Science, 2: 1-141. * 2004b Wiggins, G.B. Caddisflies: The Underwater Architects. University of Toronto Press. 2004a Wiggins, G.B. “Caddisflies: glimpses into evolutionary history.” Rotunda, 38(2): 32-39. 2002 Wiggins, G.B. “Biogeography of amphipolar caddisflies in the subfamily Dicosmoecinae (Trichoptera, Limnephilidae).” Mitteilungen aus dem Museum für Naturkunde in Berlin, Deutsche Entomologische Zeitschrift, 49(2002) 2: 227- 259. 2001 Wiggins, G.B. “Construction behavior for new pupal cases by case-making caddis larvae: Further comment. (Trichoptera: Integripalpia).” Braueria, 28: 7-9. 1999b Gall, W.K. and G.B. Wiggins. “Evidence bearing on a sister-group relationship between the families Phryganeidae and Plectrotarsidae (Trichoptera).” Proceedings of the Ninth International Symposium on Trichoptera, Chiang Mai, Thailand, 1998, edited by H. -
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. -
Appendix 11.3
APPENDIX 11.3: Macro-invertebrate diversity in Maine and northeastern U.S., by family. Maine data are from MABP database, from multiple sources. New England data (6 states, excluding New York) are from a compilation of data by Chandler and Loose (2001) that includes information for all states, but appears to focus on Massachusetts. Species totals include taxa that are identified only to genus level (i.e. genera without any species indicated). Appendices 15 Appendix 11.3 New England Taxa MABP records records Phylum Class Order Family # Genera # Spp %"Orphan" Genera *** # Genera # Spp Annelida Polychaeta Sabellida Sabellidae 00 00 Annelida Polychaeta Sabellida Aeolosomatidae 22 100 -- -- Annelida Clitellata Lumbiculida Lubriculidae 44 75 2 3 Annelida Clitellata Enchytraeida Enchytraeidae ? ? Annelida Clitellata Haplotoxida Naididae 14 35 71018 Annelida Clitellata Haplotoxida Tubificidae 612 17 5 10 Annelida Clitellata Lumbricida Glossoscolecidae -- -- Annelida Clitellata Branchiobdellida Bdellodrilidae 11 011 Annelida Clitellata Branchiobdellida Branchiobdellidae 11 011 Annelida Clitellata Branchiobdellida Cambarincolidae 24 024 Annelida Clitellata Rhynchobdellida Glossiphoniidae 77 0616 Annelida Clitellata Rhynchobdellida Piscicolidae 44 044 Annelida Clitellata Arhynchobdellida Hirudinididae 22 024 Annelida Clitellata Arhynchobdellida Erpobdellidae 45 048 Arthropoda Malacostraca Isopoda Asellidae 24 50 2 4 Arthropoda Malacostraca Amphipoda Gammaridae 11 014 Arthropoda Malacostraca Amphipoda Crangonyctidae 22 027 Arthropoda Malacostraca -
Emergence Trap Collections of Lotic Trichoptera in the Cascade Range of Oregon, U.S.A
13 EMERGENCE TRAP COLLECTIONS OF LOTIC TRICHOPTERA IN THE CASCADE RANGE OF OREGON, U.S.A. N. H. ANDERSON, R. W. WISSEMAN AND G. W. COURTNEY SUMMARY Emergence of caddisflies in three 3rd-order streams was monitored in 1982-83 using four traps, (each 3.34 m 2 ) per stream. Traps were placed over both riffle and depositional areas. A range of habitats was sampled because sites extended from 490 to 880 m in elevation and included areas with old-growth coniferous canopy, regrowth deciduous canopy and clearcut with no canopy. Although trapping efforts censused only limited reaches within each stream system, 65% of all caddis species known from the drainage were obtained. More than 5200 specimens were collected. Rhyacophilidae (23 species) and Limnephilidae (14 species) were the most diverse families, but Lepidostomatidae accounted for 46% of the individuals, followed by Philopotamidae (14%), and Rhyacophilidae (13%). When partitioned into functional feeding groups, scrapers were the most diverse group; whereas collectors were poorly represented. INTRODUCTION This project is part of a comprehensive study of the impact of riparian vegetation on the structure and function of stream ecosystems in the Western Coniferous Forest Biome. Emergence trap collections of aquatic insects are being used as an index of secondary production to compare the biota of streams flowing through old-growth coniferous forest, a recent clearcut, and a regrowth deciduous forest. We present data for one flight season (1982-83) on species composition, abundance, functional feeding groups and seasonal occurrence of caddisflies. In a subsequent paper, we will analyze differences among sites for the entire insect community. -
Macroinvertebrate Inventory of the Caspar Creek Watershed
FINAL REPORT: Macroinvertebrate Inventory of the Caspar Creek Watershed Kenneth W. Cummins1 and David Malkauskas2 1. California Cooperative Fisheries Research Unit, Humboldt State University 2. Department of Entomology, Michigan State University 1 Introduction A macroinvertebrate assessment was conducted on the Caspar Creek Experimental Watershed in northwestern California using a functional feeding group (FFG) classification. The approach, developed over 30 years ago (Cummins 1973), has been tested, modified, and employed in many studies (e.g. Cummins and Klug 1979, Cummins and Wilzbach 1985), Merritt and Cummins 2006). The approach categorizes macroinvertebrates based on their morphological and behavioral mechanisms by which they acquire one or more of six general food types: coarse particulate organic matter (CPOM), fine particulate organic matter (FPOM), periphytic, non-filamentous algae and associated bio-film, invertebrate prey organisms, and filamentous algae (Table 1). The morpho-behavioral adaptations of stream macroinvertebrates for acquiring food are easily observed in the field on live specimens. An example is the large eyes, bright color patterns, and active movement that characterize the three predaceous stonefly families (setipalpian Plecoptera). The abundance (especially expressed as biomass) of any FFG is an indicator of the relative availability of its food resource category. The method has the advantage that the survey crew leaves the field with the data as well as with preserved samples that can be analyzed in taxonomic data, and measured for biomass conversion calculations in the lab, if (and this is almost always the problem) funds are available for the very time-consuming process of microscope analysis. The point is, that a great deal of information about the status of a stream ecosystem can be obtained in the field using the FFG approach, but it does not for close the ability to analyze the samples in the lab. -
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 -
Arthropod Prey for Riparian Associated Birds in Headwater Forests of the Oregon Coast Range ⇑ Joan C
Forest Ecology and Management 285 (2012) 213–226 Contents lists available at SciVerse ScienceDirect Forest Ecology and Management journal homepage: www.elsevier.com/locate/foreco Arthropod prey for riparian associated birds in headwater forests of the Oregon Coast Range ⇑ Joan C. Hagar a, , Judith Li b,1, Janel Sobota b,1, Stephanie Jenkins c,2 a US Geological Survey Forest & Rangeland Ecosystem Science Center, 3200 SW Jefferson Way, Corvallis, OR 97331, United States b Oregon State University, Department of Fisheries & Wildlife, Nash Hall, Room #104, Oregon State University, Corvallis, OR 97331-3803, United States c Oregon State University, Department of Forest Ecosystems & Society, 321 Richardson Hall, Corvallis, OR 97331, United States article info abstract Article history: Headwater riparian areas occupy a large proportion of the land base in Pacific Northwest forests, and thus Received 11 May 2012 are ecologically and economically important. Although a primary goal of management along small head- Received in revised form 16 August 2012 water streams is the protection of aquatic resources, streamside habitat also is important for many ter- Accepted 19 August 2012 restrial wildlife species. However, mechanisms underlying the riparian associations of some terrestrial Available online 21 September 2012 species have not been well studied, particularly for headwater drainages. We investigated the diets of and food availability for four bird species associated with riparian habitats in montane coastal forests Keywords: of western Oregon, USA. We examined variation in the availability of arthropod prey as a function of dis- Aquatic-terrestrial interface tance from stream. Specifically, we tested the hypotheses that (1) emergent aquatic insects were a food Arthropod prey Forest birds source for insectivorous birds in headwater riparian areas, and (2) the abundances of aquatic and terres- Headwater streams trial arthropod prey did not differ between streamside and upland areas during the bird breeding season. -
Field Key for Selected Benthic Invertebrates from the Hkh Region
FIELD KEY FOR SELECTED BENTHIC INVERTEBRATES FROM THE HKH REGION DRAFT VERSION FEBRUARY 2007 prepared by Anne Hartmann TRICHOPTERA Family Brachycentridae - Cylindrical case of plant or mineral material - Small to medium sized - Pronotum sometimes with rim 2 Genera: Micrasema & Brachycentrus Brachycentrus sp. Micrasema sp. - Pro- & mesonotum fully sclerotised - Pro- & mesonotum fully sclerotised - 9th tergit sclerotized - 9th tergit sclerotized - mid- & hind legs elongated - mid- & hind legs normal - medium sized - case with necking - small sized Brachycentridae: Braychycentrus Brachycentridae: Micrasema „Typ1“ Brachycentridae: Braychcentrus Brachycentridae: Micrasema „Typ2“ TRICHOPTERA Family Calamotoceridae Anisocentropus sp. - Case made of 2 leaves Hind legs elongated and tibiae subdivided - Pronotum pointed on anterior margin Calamotoceridae: Anisocentropus Calamotoceridae: Anisocentropus Calamotoceridae: Anisocentropus Calamotoceridae: Anisocentropus TRICHOPTERA Family Glossosomatidae - Turtle- like case 2 Subfamilies: Glossosomatinae & Agapetinae Glossosomatinae Agapetinae sclerites on pronotum only with sclerites on meso- & metano- tum Glossosomatidae: Glossosomatinae Glossosomatidae: Agapetinae Glossosomatidae: Glossosomatinae Glossosomatidae: Agapetinae This figure means, that for identifying the taxon in the field the use of a magnifying glass is recommended TRICHOPTERA Family Goeridae - 9th tergite not sclerotized with prosternal horn - mesonotum fully sclerotised, - epipleuron with large process - metanotum with 6 small sclerites -
Of the Sharr Mountains in Kosovo
Ecologica Montenegrina 23: 40-46 (2019) This journal is available online at: www.biotaxa.org/em New additions to the caddisfly fauna (Insecta: Trichoptera) of the Sharr Mountains in Kosovo HALIL IBRAHIMI1, RUZHDI KUÇI2*, ERËMIRA GASHI1, ASTRIT BILALLI3, MILAIM MUSLIU3, VALMIR VEHAPI1, AGIM GASHI1, LINDA GRAPCI – KOTORI1 & DONARD GECI1 1Department of Biology, Faculty of Mathematics and Natural Sciences, University of Prishtina, Mother Teresa street p.n., 10000 Prishtina, Kosovo 2Faculty of Education, University of Prishtina “Hasan Prishtina”, “Agim Ramadani” street p.n., 10000 Prishtina, Republic of Kosovo 3University of Peja “Haxhi Zeka”, Faculty of Agribusiness, Street “UÇK” 30000 Pejë, Kosovo *Corresponding author: [email protected] Received 15 June 2019 │ Accepted by V. Pešić: 20 September 2019 │ Published online 16 October 2019 Abstract Adult caddisflies were collected in the Opojë Region belonging to the Sharr Mountains in Kosovo from May to October 2013. This mountainous area which is known for many endemic and rare species of plants and animals is still not enough explored in terms of caddisfly fauna. A diverse fauna consisting of 11 families and 43 species was found. Three species found during this investigation are first records for the Kosovo caddisfly fauna: Limnephilus lunatus, Micropterna lateralis and Plectrocnemia geniculata. The stenoendemic species Chaetopteroides kosovarorum is found for the second time in Kosovo. Several other rare species were recorded during this investigation. The most interesting finding is species Plectrocnemia geniculata, which is very widespread in Opojë Region and at the same time this represents one of the rarest occurrences of this species in the Balkans. This study contributes to the knowledge of the caddisfly fauna of the Sharr Mountains and adds to the list of known caddisfly species from Kosovo. -