Listed by Species Group

Total Page:16

File Type:pdf, Size:1020Kb

Listed by Species Group Species Observed at Fifth Metchosin BioBlitz, June 13, 2015 List of all species by species group as of July 14, 2015 Species Latin Species English if Reported Species Main Group Species Subgroup BC Status Frullania tamarisci Bryophyte Liverwort Lepidozia reptans Little Hands Liverwort Bryophyte Liverwort Lophocolea bidentata Bryophyte Liverwort Plagiochila porelloides Bryophyte Liverwort Porella navicularis Bryophyte Liverwort Amphidium californicum Bryophyte Moss Antitrichia curtipendula Bryophyte Moss Aulacomnium androgynum Bryophyte Moss Buckiella undulata Bryophyte Moss Claopodium bolanderi Bryophyte Moss Dicranoweisia cirrata Bryophyte Moss Dicranoweisia crispa Bryophyte Moss Dicranum fuscescens Dusky Fork,Curly Heron’s-bill Bryophyte Moss Dicranum howellii Bryophyte Moss Dicranum scoparium Bryophyte Moss Dicranum tauricum Bryophyte Moss Fontinalis neomexicana Water Moss Bryophyte Moss Homalothecium fulgescens Bryophyte Moss Hylocomium splendens Bryophyte Moss Hypnum circinale Bryophyte Moss Hypnum subimponens Bryophyte Moss Isothecium cristatum Bryophyte Moss Isothecium stoloniferum Bryophyte Moss Kindbergia oregana Bryophyte Moss Kindbergia praelonga Bryophyte Moss Leucolepis acanthoneura Bryophyte Moss Neckera menziesii Bryophyte Moss Orthotrichum lyellii Bryophyte Moss Plagiomnium insigne Badge Moss Bryophyte Moss Plagiomnium venustum Bryophyte Moss Pohlia cruda Bryophyte Moss Polytrichum juniperinum Bryophyte Moss Prhytidiadelphus triquetrus Bryophyte Moss Racomitrium elongatum Bryophyte Moss Rhizomnium glabrescens Fan Moss Bryophyte Moss Rhytidiadelphus loreus Bryophyte Moss Rhytidiadelphus triquetrus Bryophyte Moss Scleropodium obtusifolium Blunt-leafed Moss Bryophyte Moss Trachybryum megaptilum Bryophyte Moss Ulota obtusiuscula Bryophyte Moss Bisporella sulfurina Fungus Ceriporia reticulata Fungus Coccomyces dentatus Fungus Coccomyces dentatus Fungus Coccomyces tumidus Fungus Didymascella thujina Fungus Fomitopsis pinicola Red belt Fungus Ganoderma applanatum Fungus Hemimycena tortuosa Fungus Hygrocybe miniata Fungus Hymenoscyphus imberbis Fungus Hypomyces aurantius Fungus Hysterangium sp Fungus Lachnum pudibundum Fungus Lachnum virgineum Fungus Laricifomes officinalis Fungus Lycoperdon foetidum Fungus Mollisia cinerea Fungus Mollisia ventosa Fungus Mycena delicatella Fungus Myriosclerotinia sp. Fungus Nidula niveotomentosa Fungus Orbilia delicatulla Fungus Peniophora sp Fungus Phaeolus schweinitzii Fungus Phellinus ferreus Fungus Phellinus pini Fungus Pirex concentricus Fungus Pleurotus ostreatus oyster mushroom Fungus Pluteus cervinus Fungus Scutellinia umbrorum Fungus Stereum hirsutum Fungus Tapinella panuoides Fungus Trametes versicolor Fungus Trichaptum abietinum Silver Leaf Fungus Trichaptum abietinum Fungus Xylaria hypoxylon Fungus Aphaenogaster occidentalis Spine-waisted Ant Invertebrate Hymenoptera Bembix americana Sand Wasp Invertebrate Hymenoptera Coelioxys sp Invertebrate Hymenoptera Formica obscuripes Thatching Ant Invertebrate Hymenoptera Philanthus sp Invertebrate Hymenoptera Vespula vulgaris yellow jacket Invertebrate Hymenoptera Acronicta perdita Invertebrate Lepidoptera Aglais milberti Milbert's Tortoiseshell Invertebrate Lepidoptera Anavitrinella pampinaria Common Gray Invertebrate Lepidoptera Antheraea polyphemus Polyphemus Moth Invertebrate Lepidoptera Archips rosana Invertebrate Lepidoptera Biston betularia Pepper & Salt Geometer Invertebrate Lepidoptera Callizzia amorata Gray Scoopwing Invertebrate Lepidoptera Campaea perlata Pale Beauty Invertebrate Lepidoptera Caradrina morpheus Mottled Rustic Invertebrate Lepidoptera Celastrina echo Western spring azure Invertebrate Lepidoptera Chrysoteuchia topiaria Cranberry Girdler Invertebrate Lepidoptera Coenonympha tullia Vancouver Island Ringlet Invertebrate Lepidoptera red Cyclophora dataria Invertebrate Lepidoptera Cyclophora pendulinaria Sweetfern Geometer Invertebrate Lepidoptera Cydia pomonella Apple Codling Moth Invertebrate Lepidoptera Drepanulatrix sp Invertebrate Lepidoptera Enypia packardata Packard's Girdle Invertebrate Lepidoptera Eudonia commortalis Invertebrate Lepidoptera Eupithecia longipalpata Invertebrate Lepidoptera Feralia deceptiva Deceptive Sallow Invertebrate Lepidoptera Gluphisia septentrionis Common Gluphisia Invertebrate Lepidoptera Hesperumia sulphuraria Sulphur Moth Invertebrate Lepidoptera Homorthodes hanhami Invertebrate Lepidoptera Hyalophora euryalus Ceanothus Silkmoth Invertebrate Lepidoptera Hyppa contrasta Invertebrate Lepidoptera Idaea dimidiata Single-dotted Wave Moth Invertebrate Lepidoptera Iridopsis larvaria Bent-line Gray Invertebrate Lepidoptera Lacinipolia cuneata Cuneate Arches Invertebrate Lepidoptera Lacinipolia patalis Invertebrate Lepidoptera Leucania dia Invertebrate Lepidoptera Lobophora nivigerata Invertebrate Lepidoptera Lophocampa maculata Spotted Tussock Invertebrate Lepidoptera Macaria signaria Pale-marked Angle Invertebrate Lepidoptera Myelopsis subtetricella Invertebrate Lepidoptera Nadata gibbosa White-dotted Prominent Invertebrate Lepidoptera Nemoria darwiniata Columbian Emerald Invertebrate Lepidoptera Noctua pronuba Large Yellow Underwing Invertebrate Lepidoptera Pandemis cerasana Invertebrate Lepidoptera Pasiphila rectangulata Green Pug Invertebrate Lepidoptera Perizoma curvilinea Invertebrate Lepidoptera Perizoma grandis Invertebrate Lepidoptera Pheosia rimosa Black-rimmed Prominent Invertebrate Lepidoptera Protitame matilda Invertebrate Lepidoptera Protodeltote albidula Pale Glyph Invertebrate Lepidoptera Schizura ipomoeae Morning-Glory Prominent Invertebrate Lepidoptera Schizura unicornis Unicorn Caterpillar Moth Invertebrate Lepidoptera Spilosoma virginica Virginian Tiger Moth Invertebrate Lepidoptera Stenoporpia excelsaria Invertebrate Lepidoptera Thymelicus lineola European Skipper Invertebrate Lepidoptera Tortricidae (Family) Invertebrate Lepidoptera Trichordestra liquida Invertebrate Lepidoptera Tyria jacobaeae Cinnabar Moth Invertebrate Lepidoptera Vanessa atalanta Red Admiral Invertebrate Lepidoptera Venusia obsoleta Invertebrate Lepidoptera Yponomeuta padella Invertebrate Lepidoptera Bruchidius villosus Broom Seed Beetle Invertebrate Other insects Camnula pelucida Clear-winged Grasshopper Invertebrate Other insects Centrodera spurca Yellow Douglas Fir Borer Invertebrate Other insects Closterotomus norvegicus Potato Bug Invertebrate Other insects Coccinella septempunctata Seven-spotted Lady Beetle Invertebrate Other insects Coniontis ovalis Invertebrate Other insects Diplotaxis sp Invertebrate Other insects Elateridae (Family) Invertebrate Other insects Eleodes sp Invertebrate Other insects Enallagma annexum Damselfly Invertebrate Other insects Grammoptera haematites Invertebrate Other insects Hemerobius sp. Invertebrate Other insects Melanoplus sanguinipes Migratory Grasshopper Invertebrate Other insects Philaenus spumarius Meadow Spittle Bug Invertebrate Other insects Podabrus sp Invertebrate Other insects Polyphylla sp. Scarab beetle Invertebrate Other insects Pterostichus sp Invertebrate Other insects Reticulitermes hesperus Western Subterranean Termite Invertebrate Other insects Scytonotus granulatus Millipede Invertebrate Other insects Tabanidae (Family) Deer Fly Invertebrate Other insects Ariolomax columbiana banana slug Invertebrate Slug Alectoria sarmentosa Lichen Cladonia bellidiflora Lipstick lichen Lichen Cladonia furcata Lichen Cladonia macilenta Lichen Evernia prunastri Lichen Hypogymnia enteromorpha Lichen Hypogymnia imshaugii Lichen Hypogymnia physodes Lichen Lepraria sp. Lichen Loxosporopsis corallifera Lichen Mycoblastus sanguinarius Lichen Ochrolechia laevigata Lichen Ochrolechia oregonensis Lichen Parmelia hygrophila Lichen Peltigera britannica Lichen Pertusaria amara Lichen Pertusaria ophthalmiza Lichen Platismatia glauca Lichen Platismatia herrei Lichen Sphaerophorus globosus Lichen Umbilicaria deusta Lichen Usnea filipendula Lichen Usnea subfloridana Lichen Fuligo septica Scrambled egg slime mold Slime mold Stemonitis sp. Slime mold Athyrium felix-femina Vascular plant Fern Blechnum spicant deer fern Vascular plant Fern Dryopteris expansa spiny wood fern Vascular plant Fern Pentagramma triangularis Vascular plant Fern Polypodium glycyrhiza Vascular plant Fern Polystichum munitum Vascular plant Fern Pteridium aquilinum Vascular plant Fern Abronia latifolia Vascular plant Forb Blue Achillea millefolium Vascular plant Forb Achlys triphylla Vascular plant Forb Acmispon americanus Vascular plant Forb Acmispon parviflorus Vascular plant Forb Adenocaulon bicolor Pathfinder Vascular plant Forb Agoseris grandiflora Vascular plant Forb Allium acuminatum Vascular plant Forb Allium cernuum Vascular plant Forb Allotropa virgata Vascular plant Forb Ambrosia chamissonis Vascular plant Forb Anaphalis margaritacea Vascular plant Forb Anemone lyallii Vascular plant Forb Anisocarpus madioides Vascular plant Forb Anthriscus caucalis Vascular plant Forb Boschniakia hookeri Vascular plant Forb Brodiaea coronaria Vascular plant Forb Cakile maritima Vascular plant Forb Calypso bulbosa Vascular plant Forb Camassia quamash Vascular plant Forb Camissonia contorta Contorted-pod evening primrose Vascular plant Forb Red Campanula scouleri Vascular plant Forb Cardamine pensylvanica Vascular plant Forb Cerastium arvense Vascular plant Forb Cerastium glomeratum Vascular plant Forb Chenopodium album Vascular plant Forb Cirsium arvense Vascular plant Forb Cirsium vulgare Vascular plant Forb Clarkia amoena Vascular plant Forb Blue Claytonia perfoliata Vascular plant Forb Claytonia
Recommended publications
  • Diversity of Fungal Assemblages in Roots of Ericaceae in Two
    Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems Ahlam Hamim, Lucie Miche, Ahmed Douaik, Rachid Mrabet, Ahmed Ouhammou, Robin Duponnois, Mohamed Hafidi To cite this version: Ahlam Hamim, Lucie Miche, Ahmed Douaik, Rachid Mrabet, Ahmed Ouhammou, et al.. Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems. Comptes Rendus Biologies, Elsevier Masson, 2017, 340 (4), pp.226-237. 10.1016/j.crvi.2017.02.003. hal- 01681523 HAL Id: hal-01681523 https://hal.archives-ouvertes.fr/hal-01681523 Submitted on 23 Apr 2018 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. See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/315062117 Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems Article in Comptes rendus biologies · March 2017 DOI: 10.1016/j.crvi.2017.02.003 CITATIONS READS 0 37 7 authors, including: Ahmed Douaik Rachid Mrabet Institut National de Recherche Agronomique
    [Show full text]
  • Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), Michigan: VI
    The Great Lakes Entomologist Volume 35 Number 1 - Spring/Summer 2002 Number 1 - Article 10 Spring/Summer 2002 April 2002 Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), Michigan: VI. Miscellaneous Small Families (Lepidoptera) Edward G. Voss University of Michigan Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Voss, Edward G. 2002. "Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), Michigan: VI. Miscellaneous Small Families (Lepidoptera)," The Great Lakes Entomologist, vol 35 (1) Available at: https://scholar.valpo.edu/tgle/vol35/iss1/10 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Voss: Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), 2002 THE GREAT LAKES ENTOMOLOGIST 53 MOTHS OF THE DOUGLAS LAKE REGION (EMMET AND CHEBOYGAN COUNTIES), MICHIGAN: VI. MISCELLANEOUS SMALL FAMILIES (LEPIDOPTERA) Edward G. Voss1 ABSTRACT Forty-seven species in nine families of Lepidoptera (Hepialidae, Psychidae, Alucitidae, Sesiidae, Cossidae, Limacodidae, Thyrididae, Pterophoridae, Epiplemi- dae) are listed with earliest and latest recorded flight dates in Emmet and Cheboy- gan counties, which share the northern tip of the Lower Peninsula of Michigan. The records are from the principal institutional and private collections of Michigan moths and continue the documented listing of Lepidoptera in the region. ____________________ Emmet and Cheboygan counties share the northern tip of the Lower Peninsula of Michigan, the former bordered on the west by Lake Michigan and the latter, on the east by Lake Huron.
    [Show full text]
  • The Fungi of Slapton Ley National Nature Reserve and Environs
    THE FUNGI OF SLAPTON LEY NATIONAL NATURE RESERVE AND ENVIRONS APRIL 2019 Image © Visit South Devon ASCOMYCOTA Order Family Name Abrothallales Abrothallaceae Abrothallus microspermus CY (IMI 164972 p.p., 296950), DM (IMI 279667, 279668, 362458), N4 (IMI 251260), Wood (IMI 400386), on thalli of Parmelia caperata and P. perlata. Mainly as the anamorph <it Abrothallus parmeliarum C, CY (IMI 164972), DM (IMI 159809, 159865), F1 (IMI 159892), 2, G2, H, I1 (IMI 188770), J2, N4 (IMI 166730), SV, on thalli of Parmelia carporrhizans, P Abrothallus parmotrematis DM, on Parmelia perlata, 1990, D.L. Hawksworth (IMI 400397, as Vouauxiomyces sp.) Abrothallus suecicus DM (IMI 194098); on apothecia of Ramalina fustigiata with st. conid. Phoma ranalinae Nordin; rare. (L2) Abrothallus usneae (as A. parmeliarum p.p.; L2) Acarosporales Acarosporaceae Acarospora fuscata H, on siliceous slabs (L1); CH, 1996, T. Chester. Polysporina simplex CH, 1996, T. Chester. Sarcogyne regularis CH, 1996, T. Chester; N4, on concrete posts; very rare (L1). Trimmatothelopsis B (IMI 152818), on granite memorial (L1) [EXTINCT] smaragdula Acrospermales Acrospermaceae Acrospermum compressum DM (IMI 194111), I1, S (IMI 18286a), on dead Urtica stems (L2); CY, on Urtica dioica stem, 1995, JLT. Acrospermum graminum I1, on Phragmites debris, 1990, M. Marsden (K). Amphisphaeriales Amphisphaeriaceae Beltraniella pirozynskii D1 (IMI 362071a), on Quercus ilex. Ceratosporium fuscescens I1 (IMI 188771c); J1 (IMI 362085), on dead Ulex stems. (L2) Ceriophora palustris F2 (IMI 186857); on dead Carex puniculata leaves. (L2) Lepteutypa cupressi SV (IMI 184280); on dying Thuja leaves. (L2) Monographella cucumerina (IMI 362759), on Myriophyllum spicatum; DM (IMI 192452); isol. ex vole dung. (L2); (IMI 360147, 360148, 361543, 361544, 361546).
    [Show full text]
  • A Comprehensive DNA Barcode Library for the Looper Moths (Lepidoptera: Geometridae) of British Columbia, Canada
    AComprehensiveDNABarcodeLibraryfortheLooper Moths (Lepidoptera: Geometridae) of British Columbia, Canada Jeremy R. deWaard1,2*, Paul D. N. Hebert3, Leland M. Humble1,4 1 Department of Forest Sciences, University of British Columbia, Vancouver, British Columbia, Canada, 2 Entomology, Royal British Columbia Museum, Victoria, British Columbia, Canada, 3 Biodiversity Institute of Ontario, University of Guelph, Guelph, Ontario, Canada, 4 Canadian Forest Service, Natural Resources Canada, Victoria, British Columbia, Canada Abstract Background: The construction of comprehensive reference libraries is essential to foster the development of DNA barcoding as a tool for monitoring biodiversity and detecting invasive species. The looper moths of British Columbia (BC), Canada present a challenging case for species discrimination via DNA barcoding due to their considerable diversity and limited taxonomic maturity. Methodology/Principal Findings: By analyzing specimens held in national and regional natural history collections, we assemble barcode records from representatives of 400 species from BC and surrounding provinces, territories and states. Sequence variation in the barcode region unambiguously discriminates over 93% of these 400 geometrid species. However, a final estimate of resolution success awaits detailed taxonomic analysis of 48 species where patterns of barcode variation suggest cases of cryptic species, unrecognized synonymy as well as young species. Conclusions/Significance: A catalog of these taxa meriting further taxonomic investigation is presented as well as the supplemental information needed to facilitate these investigations. Citation: deWaard JR, Hebert PDN, Humble LM (2011) A Comprehensive DNA Barcode Library for the Looper Moths (Lepidoptera: Geometridae) of British Columbia, Canada. PLoS ONE 6(3): e18290. doi:10.1371/journal.pone.0018290 Editor: Sergios-Orestis Kolokotronis, American Museum of Natural History, United States of America Received August 31, 2010; Accepted March 2, 2011; Published March 28, 2011 Copyright: ß 2011 deWaard et al.
    [Show full text]
  • Influence of Habitat and Bat Activity on Moth Community Composition and Seasonal Phenology Across Habitat Types
    INFLUENCE OF HABITAT AND BAT ACTIVITY ON MOTH COMMUNITY COMPOSITION AND SEASONAL PHENOLOGY ACROSS HABITAT TYPES BY MATTHEW SAFFORD THESIS Submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology in the Graduate College of the University of Illinois at Urbana-Champaign, 2018 Urbana, Illinois Advisor: Assistant Professor Alexandra Harmon-Threatt, Chair and Director of Research ABSTRACT Understanding the factors that influence moth diversity and abundance is important for monitoring moth biodiversity and developing conservation strategies. Studies of moth habitat use have primarily focused on access to host plants used by specific moth species. How vegetation structure influences moth communities within and between habitats and mediates the activity of insectivorous bats is understudied. Previous research into the impact of bat activity on moths has primarily focused on interactions in a single habitat type or a single moth species of interest, leaving a large knowledge gap on how habitat structure and bat activity influence the composition of moth communities across habitat types. I conducted monthly surveys at sites in two habitat types, restoration prairie and forest. Moths were collected using black light bucket traps and identified to species. Bat echolocation calls were recorded using ultrasonic detectors and classified into phonic groups to understand how moth community responds to the presence of these predators. Plant diversity and habitat structure variables, including tree diameter at breast height, ground cover, and vegetation height were measured during summer surveys to document how differences in habitat structure between and within habitats influences moth diversity. I found that moth communities vary significantly between habitat types.
    [Show full text]
  • <I>Coccomyces</I> with Dimorphic Paraphyses
    ISSN (print) 0093-4666 © 2014. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/129.297 Volume 129(2), pp. 297–302 October–December 2014 A new species of Coccomyces with dimorphic paraphyses Xiao-Yan Wang1, Hai-Lin Gu1, Qing Li1, Lei-Hong Wang2, & Ying-Ren Lin2* 1 School of Life Science & 2 School of Forestry & Landscape Architecture, Anhui Agricultural University, West Changjiang Road 130, Hefei, Anhui 230036, China *Correspondence to: [email protected] Abstract — A new Coccomyces species found on fallen leaves of Millettia dielsiana at Mt Sanqingshan, Jiangxi province, China, is described as Coccomyces alienus. This taxon is distinguished from all other Coccomyces taxa by having two types of paraphyses. The type specimen is deposited in the Reference Collection of Forest Fungi of Anhui Agricultural University, China (AAUF). Key words — foliicolous fungus, taxonomy, Fabaceae, fungal diversity Introduction Coccomyces De Not. is the second-largest genus in the Rhytismataceae (Rhytismatales, Leotiomycetes, Ascomycota), of which at least 116 species have been recorded (Kirk et al. 2008, Lin et al. 2012). They are widely distributed and occur on leaves, herbaceous stems, bark, and wood (Sherwood 1980). The study of Coccomyces in China began in 1934 with the records of C. dentatus on Quercus and Castanea, and C. delta (Kunze) Sacc. on Lauraceae (Teng 1934). Subsequently, twenty-eight additional species have been reported (Korf & Zhuang 1985; Lin et al. 1994; Lin 1998; Hou et al. 2006, 2007; Jia et al. 2012; Zheng et al. 2012; Wang et al. 2013; Yang et al. 2013). Of the 159 fungal species known to inhabit Millettia, no Coccomyces species has yet been reported on this plant genus (Farr & Rossman 2014).
    [Show full text]
  • Coccomyces Dentatus (J.C
    Coccomyces dentatus (J.C. Schmidt & Kunze) Sacc., Michelia 1(no. 1): 59 (1877) COROLOGíA Registro/Herbario Fecha Lugar Hábitat MAR-180409 175 18/04/2009 Río Guadalix, Puente de San Sobre hojas caídas Leg.: Fermín Pancorbo, José Antonio, Dehesa de Moncalvillo de encina (Quercus Cuesta, Miguel Á. Ribes (San Agustín del Guadalix) ilex) Det.: Miguel Á. Ribes 650 m. 30T VL4834 TAXONOMíA Basiónimo: Phacidium dentatum J.C. Schmidt (1817) Citas en listas publicadas: Saccardo's Syll. fung. III: 628; VIII: 745; XII: 117; XVIII: 164; XIX: 362; XXII: 750. Posición en la clasificación: Rhytismataceae, Rhytismatales, Leotiomycetidae, Leotiomycetes, Ascomycota, Fung Sinónimos: o Coccomyces bromeliacearum Theiss., Beih. bot. Zbl., Abt. 1 27: 407 (1910) o Coccomyces dentatus f. Lauri Rehm, in Theissen, Beih. bot. Zbl., Abt. 1 27: 406 (1910) o Coccomyces filicicola Speg., Boletín de la Academia Nacional de Ciencias de Córdoba 23(3-4): 514 (1919) o Coccomyces pentagonus Kirschst., Annls mycol. 34: 208 (1936) o Leptostroma quercinum Lasch, in Klotzsch, Klotzsch Herb. Myc.: no. 1075 (1845) o Leptothyrium castaneae var. quercus C. Massal. o Leptothyrium quercinum (Lasch) Sacc., Michelia 2(no. 6): 113 (1880) o Lophodermium dentatum (J.C. Schmidt & Kunze) De Not., G. bot. ital., n.s. 2(7-8): 43 (1847) o Phacidium dentatum J.C. Schmidt, Mykologische Hefte (Leipzig) 1: 41 (1817) DESCRIPCIÓN MACRO Apotecios de aproximadamente 1 mm, formando una capa estromática pardo-grisácea, en forma de pentágono (a veces sólo con 4 lados), que al madurar forman 4-5 fisuras lineales radiales, dejando ver el himenio de color grisáceo. Sobre las hojas en las que fructifican forman manchas más claras, en forma de mosaico y delimitadas por una línea negra, pero el resto de la hoja suele estar intacta y con su color original.
    [Show full text]
  • Beginner S Guide to Moths of the Midwest Geometers
    0LGZHVW5HJLRQ86$ %HJLQQHU V*XLGHWR0RWKVRIWKH0LGZHVW*HRPHWHUV $QJHOOD0RRUHKRXVH ,OOLQRLV1DWXUH3UHVHUYH&RPPLVVLRQ Photos: Angella Moorehouse ([email protected]). Produced by: Angella Moorehouse with the assistance of Alicia Diaz, Field Museum. Identification assistance provided by: multiple sources (inaturalist.org; bugguide.net) )LHOG0XVHXP &&%<1&/LFHQVHGZRUNVDUHIUHHWRXVHVKDUHUHPL[ZLWKDWWULEXWLRQEXWFRPPHUFLDOXVHRIWKHRULJLQDOZRUN LVQRWSHUPLWWHG >ILHOGJXLGHVILHOGPXVHXPRUJ@>@YHUVLRQ $ERXWWKH%(*,11(5¶6027+62)7+(0,':(67*8,'(6 Most photos were taken in west-central and central Illinois; a fewDUH from eastern Iowa and north-central Wisconsin. Nearly all were posted to identification websites: BugGuide.netDQG iNaturalist.org. Identification help was provided by Aaron Hunt, Steve Nanz, John and Jane Balaban, Chris Grinter, Frank Hitchell, Jason Dombroskie, William H. Taft, Jim Wiker,DQGTerry Harrison as well as others contributing to the websites. Attempts were made to obtain expert verifications for all photos to the field identification level, however, there will be errors. Please contact the author with all corrections Additional assistance was provided by longtime Lepidoptera survey partner, Susan Hargrove. The intention of these guides is to provide the means to compare photographs of living specimens of related moths from the Midwest to aid the citizen scientists with identification in the field for Bio Blitz, Moth-ers Day, and other night lighting events. A taxonomic list to all the species featured is provided at the end along with some field identification tips. :(%6,7(63529,',1*,'(17,),&$7,21,1)250$7,21 BugGuide.net LNaturalist.org Mothphotographersgroup.msstate.edu Insectsofiowa.org centralillinoisinsects.org/weblog/resources/ :+,&+027+*8,'(7286( The moths were split into 6 groups for the purposes of creating smaller guides focusing on similar features of 1 or more superfamilies.
    [Show full text]
  • 1 Appendix 3. Pacific Rim National Park Taxonomy Report
    Appendix 3. Pacific Rim National Park Taxonomy Report Class Order Family Genus Species Anopla Heteronemertea Lineidae Cerebratulus Arachnida Araneae Amaurobiidae Callobius Callobius pictus Araneidae Larinioides Larinioides patagiatus Clubionidae Clubiona Clubiona pacifica Clubiona pallidula Clubiona trivialis Corinnidae Castianeira Castianeira variata Cybaeidae Cybaeus Cybaeus reticulatus Hahniidae Dirksia Dirksia cinctipes Ethobuella Ethobuella tuonops Linyphiidae Agyneta Agyneta darrelli cf. Bathyphantes Bathyphantes keeni Bathyphantes orica Ceraticelus Ceraticelus silus Ceratinops Ceratinops inflatus Linyphantes Linyphantes orcinus Linyphantes pacificus Microlinyphia Microlinyphia dana Neriene Neriene digna Pityohyphantes Pityohyphantes alticeps 1 Pityohyphantes cristatus Pocadicnemis Pocadicnemis pumila Scotinotylus Scotinotylus patellatus Semljicola Semljicola sp. 3GAB Sisicottus Sisicottus montanus Sisicottus nesides Symmigma Symmigma minimum Tachygyna Tachygyna ursina Tenuiphantes Tenuiphantes zelatus Tenuiphantes zibus Walckenaeria Walckenaeria directa Zygottus Zygottus corvallis Lycosidae Pardosa Pardosa dorsuncata Pardosa mackenziana Nesticidae Nesticus Nesticus silvestrii Philodromidae Philodromus Philodromus dispar Phrurolithidae Phrurotimpus Phrurotimpus borealis Pimoidae Pimoa Pimoa altioculata Salticidae Evarcha Evarcha hoyi Tetragnathidae Metellina Metellina curtisi Tetragnatha Tetragnatha laboriosa Theridiidae Enoplognatha Enoplognatha ovata Rugathodes Rugathodes sexpunctatus 2 Theridion Theridion californicum Theridion
    [Show full text]
  • (Name) (Degree) (Major) Date Thesis Is Presented
    AN ABSTRACT OF THE THESIS OF Anthony Noel McFarland for the M.S. in Entomology (Name) (Degree) ------~~~~~-------(Major) - Date thesis is presented May 10, 1963 ------~--~~-------- Title THE MACROHETEROCERA (LEPIDOPTERA) OF Abstract approved / A continuous twenty-month survey of the Macroheterocera (Lepidoptera) occurring at a location in McDonald Forest, five miles northwest of Corvallis, Benton County, Oregon was conducted. Three hundred sixty species of moths were collected; they repre­ sented the following families: Sphingidae, Saturniidae, Amatidae, Nolidae, Lithosiidae, Arctiidae, Agaristidae, Noctuidae, Notodonti­ dae, Liparidae, Lasiocampidae, Thyatiridae, Drepanidae, Geomet­ ridae, and Epiplemidae. Information is given on the seasonal occur­ renee, relative abundance, flight habits, and known foodplants of the species collected. Biological and behavioral information is in- eluded for 82 of the species. Comparisons are made between the local fauna and that of the northeastern United States, British Columbia, and a specific locality in southern California. A new device for attracting and holding moths more effec­ tively within the vicinity of the light (a parabolic moth sheet), which does not involve the use of a trap, is described. THE MACROHETEROCERA (LEPIDOPTERA} OFA MIXED FOREST IN WESTERN OREGON by ANTHONY NOEL McFARLAND A THESIS submitted to OREGON STATE UNIVERSITY in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE June 1963 APPROVED: In Charge of Major Chairman of Department of En Date thesis is presented May l 0, 1963 ----~--~----------- Typed by Jolene Wuest ACKNOWLEDGMENTS I wish to thank the following persons, whose assistance has been of great value: Mr. William R. Bauer and Mr. Steve Buckett of Davis, California, for determination or verification of most of the moths other than Geometrid~e.
    [Show full text]
  • Download Download
    Index to Volume 118 Compiled by Leslie Cody Abies balsamea, 46,95,124,251,268,274,361,388,401,510,530 confines, 431 lasiocarpa, 191,355,584 thomsoni, 431 Abrostola urentis, 541 Agelaius phoeniceus, 201 Acanthopteroctetes bimaculata, 532 Agelaius phoeniceus, Staging in Eastern South Dakota, Spring Acanthopteroctetidae, 532 Dispersal Patterns of Red-winged Blackbirds, 201 Acasis viridata, 539 Aglais milberti, 537 Acer,52 Agonopterix gelidella, 533 negundo, 309 Agriphila ruricolella, 536 rubrum, 41,96,136,136,251,277,361,508 vulgivagella, 536 saccharinum, 41,124,251 Agropyron spp., 400,584 saccharum, 361,507 cristatum, 300 spicatum, 362 pectiniforme, 560 Achigan à grande bouche, 523 repens, 300 à petite bouche, 523 sibiricum, 560 Achillea millefolium, 166 Agrostis sp., 169 Achnatherum richardsonii, 564 filiculmis, 558 Acipenser fulvescens, 523 gigantea, 560 Acipenseridae, 523 Aira praecox, 177 Acleris albicomana, 534 Aix sponsa, 131,230 britannia, 534 Alaska, Changes in Loon (Gavia spp.) and Red-necked Grebe celiana, 534 (Podiceps grisegena) Populations in the Lower Mata- emargana, 535 nuska-Susitna Valley, 210 forbesana, 534 Alaska, Interactions of Brown Bears, Ursus arctos, and Gray logiana, 534 Wolves, Canis lupus, at Katmai National Park and Pre- nigrolinea, 535 serve, 247 obligatoria, 534 Alaska, Seed Dispersal by Brown Bears, Ursus arctos,in schalleriana, 534 Southeastern, 499 variana, 534 Alaska, The Heather Vole, Genus Phenacomys, in, 438 Acorn, J.H., Review by, 468 Alberta: Distribution and Status, The Barred Owl, Strix varia Acossus
    [Show full text]
  • New Contributions to the Turkish Ascomycota
    Turkish Journal of Botany Turk J Bot (2018) 42: 644-652 http://journals.tubitak.gov.tr/botany/ © TÜBİTAK Research Article doi:10.3906/bot-1712-1 New contributions to the Turkish Ascomycota Abdullah KAYA*, Yasin UZUN Department of Biology, Kamil Özdağ Science Faculty, Karamanoğlu Mehmetbey University, Karaman, Turkey Received: 01.12.2017 Accepted/Published Online: 06.05.2018 Final Version: 26.09.2018 Abstract: Nine discomycete and one sordariomycete (Ascomycota) species are reported for the first time from Turkey. The genera Coccomyces, Kompsoscypha, Pseudopithyella, Strobiloscypha, and Lasiosphaeris have not been reported before in the country. Anthracobia, Plicaria, Sclerotinia, and Pithya species are new records added to the previous knowledge. Macro- and micromorphological descriptions and illustrations for each new taxon are provided. Key words: Ascomycota, biodiversity, new records, Turkey 1. Introduction Spooner (2001), Monti and Marchetti (2003), Medardi The knowledge of higher fungi in Turkey has been (2006), Peric et al. (2013), Thompson (2013), and Beug et increasing over the years. More than 2500 species has been al. (2014). identified so far in the country, and most of them have Specimens are deposited at Karamanoğlu Mehmetbey been published as checklists (Sesli and Denchev, 2014; University, Kamil Özdağ Science Faculty, Department of Solak et al., 2015). The number of taxa reached almost Biology. 210 ascomycetes. Since then, nearly 90 more species of Ascomycota were added to the former list (Akata et al., 3. Results 2016a, 2016b; Akçay and Uzun, 2016; Doğan et al., 2016; The systematics of the species are given according to Dülger and Akata, 2016; Elliot et al., 2016; Kaya, 2016; Index Fungorum (www.indexfungorum.org; accessed 30 Kaya et al., 2016; Taşkın et al., 2016; Acar and Uzun, 2017; November 2017) and Wijayawardene et al.
    [Show full text]