Evaluating a Standardized Protocol and Scale for Determining Non-Native Insect Impact
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Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
Northern Fen Communitynorthern Abstract Fen, Page 1
Northern Fen CommunityNorthern Abstract Fen, Page 1 Community Range Prevalent or likely prevalent Infrequent or likely infrequent Absent or likely absent Photo by Joshua G. Cohen Overview: Northern fen is a sedge- and rush-dominated 8,000 years. Expansion of peatlands likely occurred wetland occurring on neutral to moderately alkaline following climatic cooling, approximately 5,000 years saturated peat and/or marl influenced by groundwater ago (Heinselman 1970, Boelter and Verry 1977, Riley rich in calcium and magnesium carbonates. The 1989). community occurs north of the climatic tension zone and is found primarily where calcareous bedrock Several other natural peatland communities also underlies a thin mantle of glacial drift on flat areas or occur in Michigan and can be distinguished from shallow depressions of glacial outwash and glacial minerotrophic (nutrient-rich) northern fens, based on lakeplains and also in kettle depressions on pitted comparisons of nutrient levels, flora, canopy closure, outwash and moraines. distribution, landscape context, and groundwater influence (Kost et al. 2007). Northern fen is dominated Global and State Rank: G3G5/S3 by sedges, rushes, and grasses (Mitsch and Gosselink 2000). Additional open wetlands occurring on organic Range: Northern fen is a peatland type of glaciated soils include coastal fen, poor fen, prairie fen, bog, landscapes of the northern Great Lakes region, ranging intermittent wetland, and northern wet meadow. Bogs, from Michigan west to Minnesota and northward peat-covered wetlands raised above the surrounding into central Canada (Ontario, Manitoba, and Quebec) groundwater by an accumulation of peat, receive inputs (Gignac et al. 2000, Faber-Langendoen 2001, Amon of nutrients and water primarily from precipitation et al. -
The Canadian Entomologist
The Canadian Entomologist Vol. 107 Ottawa, Canada, March 1975 No. 3 BIOLOGICAL CONTROL ATTEMPTS BY INTRODUCTIONS AGAINST PEST INSECTS IN THE FIELD IN CANADA B. P. BEIRNE Pestology Centre, Department of Biological Sciences, Simon Fraser University, Burnaby, British Columbia Abstract Can. Ent. 107: 225-236 (1975) This is an analysis of the attempts to colonize at least 208 species of parasites and predators on about 75 species of pest insects in the field in Canada. There was colonization by about 10% of the species that were introduced in totals of under 5,000 individuals, 40% of those introduced in totals of between 5,000 and 31,200, and 78% of those introduced in totals of over 31,200. Indications exist that initial colonizations may be favoured by large releases and by selection of release sites that are semi-isolated and not ecologically complex but that colonizations are hindered when the target species differs taxonomically from the species from which introduced agents originated and when the release site lacks factors needed for introduced agents to survive or when it is subject to potentially-avoidable physical disrup- tions. There was no evidence that the probability of colonization was increased when the numbers of individuals released were increased by laboratory propagation. About 10% of the attempts were successful from the economic viewpoint. Successes may be overestimated if the influence of causes of coincidental, actual, or supposed changes in pest abundance are overlooked. Most of the successes were by two or more kinds of agents of which at least one attacked species additional to the target pests. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Coleoptera: Coccinellidae): Influence of Subelytral Ultrastructure
Experimental & Applied Acarology, 23 (1999) 97–118 Review Phoresy by Hemisarcoptes (Acari: Hemisarcoptidae) on Chilocorus (Coleoptera: Coccinellidae): influence of subelytral ultrastructure M.A. Houck* Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409–3131, USA (Received 9 January 1997; accepted 17 April 1998) ABSTRACT The non-phoretic stages of mites of the genus Hemisarcoptes are predators of the family Diaspididae. The heteromorphic deutonymph (hypopus) maintains a stenoxenic relationship with beetles of the genus Chilocorus. The mites attach to the subelytral surface of the beetle elytron during transport. There is variation in mite density among species of Chilocorus. Both Hemisarcoptes and Chilocorus have been applied to biological control programmes around the world. The objective of this study was to determine whether subelytral ultrastructure (spine density) plays a role in the evolution of symbiosis between the mite and the beetle. The subelytral surfaces of 19 species of Chilocorus and 16 species of Exochomus were examined. Spine density was determined for five subelytral zones: the anterior pronotal margin, medial central region, caudoventral tip, lateral distal margin and epipleural region. Spine density on the subelytral surface of Chilocorus and Exochomus was inversely correlated with the size of the elytron for all zones except the caudoventral tip. This suggests that an increase in body size resulted in a redistribution of spines and not an addition of spines. The pattern of spine density in Exochomus and Chilocorus follows a single size–density trajectory. The pattern of subelytral ultrastructure is not strictly consistent with either beetle phylogeny or beetle allometry. The absence of spines is not correlated with either beetle genus or size and species of either Chilocorus or Exochomus may be devoid of spines in any zone, irrespective of body size. -
Biosecurity Risk Assessment
An Invasive Risk Assessment Framework for New Animal and Plant-based Production Industries RIRDC Publication No. 11/141 RIRDCInnovation for rural Australia An Invasive Risk Assessment Framework for New Animal and Plant-based Production Industries by Dr Robert C Keogh February 2012 RIRDC Publication No. 11/141 RIRDC Project No. PRJ-007347 © 2012 Rural Industries Research and Development Corporation. All rights reserved. ISBN 978-1-74254-320-8 ISSN 1440-6845 An Invasive Risk Assessment Framework for New Animal and Plant-based Production Industries Publication No. 11/141 Project No. PRJ-007347 The information contained in this publication is intended for general use to assist public knowledge and discussion and to help improve the development of sustainable regions. You must not rely on any information contained in this publication without taking specialist advice relevant to your particular circumstances. While reasonable care has been taken in preparing this publication to ensure that information is true and correct, the Commonwealth of Australia gives no assurance as to the accuracy of any information in this publication. The Commonwealth of Australia, the Rural Industries Research and Development Corporation (RIRDC), the authors or contributors expressly disclaim, to the maximum extent permitted by law, all responsibility and liability to any person, arising directly or indirectly from any act or omission, or for any consequences of any such act or omission, made in reliance on the contents of this publication, whether or not caused by any negligence on the part of the Commonwealth of Australia, RIRDC, the authors or contributors. The Commonwealth of Australia does not necessarily endorse the views in this publication. -
Evaluating a Standardized Protocol and Scale for Determining Non-Native Insect Impact
A peer-reviewed open-access journal NeoBiota 55: 61–83 (2020) Expert assessment of non-native insect impacts 61 doi: 10.3897/neobiota.55.38981 RESEARCH ARTICLE NeoBiota http://neobiota.pensoft.net Advancing research on alien species and biological invasions The impact is in the details: evaluating a standardized protocol and scale for determining non-native insect impact Ashley N. Schulz1, Angela M. Mech2, 15, Craig R. Allen3, Matthew P. Ayres4, Kamal J.K. Gandhi5, Jessica Gurevitch6, Nathan P. Havill7, Daniel A. Herms8, Ruth A. Hufbauer9, Andrew M. Liebhold10, 11, Kenneth F. Raffa12, Michael J. Raupp13, Kathryn A. Thomas14, Patrick C. Tobin2, Travis D. Marsico1 1 Arkansas State University, Department of Biological Sciences, PO Box 599, State University, AR 72467, USA 2 University of Washington, School of Environmental and Forest Sciences, 123 Anderson Hall, 3715 W Stevens Way NE, Seattle, WA 98195, USA 3 U.S. Geological Survey, Nebraska Cooperative Fish and Wildlife Unit, University of Nebraska-Lincoln, 423 Hardin Hall, 3310 Holdrege Street, Lincoln, NE 68583, USA 4 Dartmouth College, Department of Biological Sciences, 78 College Street, Hanover, NH 03755, USA 5 The University of Georgia, Daniel B. Warnell School of Forestry and Natural Resources, 180 E. Green St., Athens, GA 30602, USA 6 Stony Brook University, Department of Ecology and Evolution, Stony Brook, NY 11794, USA 7 USDA Forest Service Northern Research Station, 51 Mill Pond Rd., Hamden, CT 06514, USA 8 The Davey Tree Expert Company, 1500 N Mantua St., Kent, OH 44240, USA -
Pathways Analysis of Invasive Plants and Insects in the Northwest Territories
PATHWAYS ANALYSIS OF INVASIVE PLANTS AND INSECTS IN THE NORTHWEST TERRITORIES Project PM 005529 NatureServe Canada K.W. Neatby Bldg 906 Carling Ave., Ottawa, ON, K1A 0C6 Prepared by Eric Snyder and Marilyn Anions NatureServe Canada for The Department of Environment and Natural Resources. Wildlife Division, Government of the Northwest Territories March 31, 2008 Citation: Snyder, E. and Anions, M. 2008. Pathways Analysis of Invasive Plants and Insects in the Northwest Territories. Report for the Department of Environment and Natural Resources, Wildlife Division, Government of the Northwest Territories. Project No: PM 005529 28 pages, 5 Appendices. Pathways Analysis of Invasive Plants and Insects in the Northwest Territories i NatureServe Canada Acknowledgements NatureServe Canada and the Government of the Northwest Territories, Department of Environment and Natural Resources, would like to acknowledge the contributions of all those who supplied information during the production of this document. Canada : Eric Allen (Canadian Forest Service), Lorna Allen (Alberta Natural Heritage Information Centre, Alberta Community Development, Parks & Protected Areas Division), Bruce Bennett (Yukon Department of Environment), Rhonda Batchelor (Northwest Territories, Transportation), Cristine Bayly (Ecology North listserve), Terri-Ann Bugg (Northwest Territories, Transportation), Doug Campbell (Saskatchewan Conservation Data Centre), Suzanne Carrière (Northwest Territories, Environment & Natural Resources), Bill Carpenter (Moraine Point Lodge, Northwest -
Coleoptera: Coccinellidae) As a Biocontrol Agent
CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources 2009 4, No. 046 Review Factors affecting utility of Chilocorus nigritus (F.) (Coleoptera: Coccinellidae) as a biocontrol agent D.J. Ponsonby* Address: Ecology Research Group, Department of Geographical and Life Sciences, Canterbury Christ Church University, North Holmes Road, Canterbury, Kent. CT1 1QU, UK. *Correspondence: Email: [email protected] Received: 30 March 2009 Accepted: 25 June 2009 doi: 10.1079/PAVSNNR20094046 The electronic version of this article is the definitive one. It is located here: http://www.cababstractsplus.org/cabreviews g CAB International 2009 (Online ISSN 1749-8848) Abstract Chilocorus nigritus (F.) has been one of the most successful coccidophagous coccinellids in the history of classical biological control. It is an effective predator of many species of Diaspididae, some Coccidae and some Asterolecaniidae, with an ability to colonize a relatively wide range of tropical and sub-tropical environments. It appears to have few natural enemies, a rapid numerical response and an excellent capacity to coexist in stable relationships with parasitoids. A great deal of literature relating to its distribution, biology, ecology, mass rearing and prey preferences exists, but there is much ambiguity and the beetle sometimes inexplicably fails to establish, even when conditions are apparently favourable. This review brings together the key research relating to factors that affect its utility in biocontrol programmes, including its use in indoor landscapes and temperate glasshouses. Data are collated and interpreted and areas where knowledge is lacking are identified. Recommendations are made for prioritizing further research and improving its use in biocontrol programmes. -
Comparison of Insect, Fungal, and Mechanically Induced Defoliation of Larch: Effects on Plant Productivity and Subsequent Host Susceptibility
Oecologia (1992) 90:411-416 Oecologia Springer-Verlag 1992 Comparison of insect, fungal, and mechanically induced defoliation of larch: effects on plant productivity and subsequent host susceptibility Steven C. Krause and Kenneth F. Raffa Department of Entomology, University of Wisconsin, Madison, WI 53706, USA Received October 16, 1991 / Accepted in revised form January 9, 1992 Summary. Larch sawfly, Pristiphora erichsonii Hartig, pathogens can also induce systemic antibiosis against and larch needlecast fungus, Mycosphaerella laricinia insect folivores (McIntyre et al. 1981), (R. Hartig) Neg., are early season defoliators restricted Fungal induced resistance to species of Coleoptera only to Larix host trees. Larch defoliation (100%) by (Ahmad et al. 1985), Hemiptera (Mathias et al. 1990), either the fungus or insect, but not mechanical removal, and Lepidoptera (Funk et al. 1983) has been demon- induced systemic responses that reduced sawfly con- strated for agronomic crops (Clay 1988). Trees infected sumption and digestion rates one year later. In a feeding with fungi may also be less susceptible to herbivory from behavior assay, larvae quickly abandoned seedlings gall-making species of Diptera (Bergdahl and Massola previously defoliated by M. laricinia. Adult female ovi- 1985), Homoptera (Lasota et al. 1983) and Hymenoptera position choice and egg deposition were unaffected. (Taper et al. 1986). Little is known, however, on the Seedling growth was not affected during the year of effects of fungal induced defoliation on free-feeding in- defoliation by M. laricinia, but was significantly reduced sect folivores and the productivity of host trees. one year later. Defoliation by M. laricinia reduced stem European larch, Larix decidua Miller, is a shade in- volume, radial growth, root biomass and new shoot tolerant, winter deciduous conifer (Olaczek 1986). -
Sawflies (Hymenoptera, Symphyta) Newly Recorded from Washington State
JHR 49: 129–159 (2016)Sawflies( Hymenoptera, Symphyta) newly recorded from Washington State 129 doi: 10.3897/JHR.49.7104 RESEARCH ARTICLE http://jhr.pensoft.net Sawflies (Hymenoptera, Symphyta) newly recorded from Washington State Chris Looney1, David R. Smith2, Sharon J. Collman3, David W. Langor4, Merrill A. Peterson5 1 Washington State Dept. of Agriculture, 1111 Washington St. SE, Olympia, Washington, 98504, USA 2 Systematic Entomology Laboratory, Agricultural Research Service, USDA, c/o National Museum of Natural History, NHB 168, Washington, D.C. 20560, USA 3 Washington State University Extension, 600 128th St. SE, Everett, Washington, 98208, USA 4 Natural Resources Canada, Canadian Forest Service, 5320 122 Street NW, Edmonton, Alberta, T6H 3S5, Canada 5 Biology Department, Western Washington University, 516 High St., Bellingham, Washington, 98225, USA Corresponding author: Chris Looney ([email protected]) Academic editor: H. Baur | Received 5 November 2015 | Accepted 27 January 2016 | Published 28 April 2016 http://zoobank.org/319E4CAA-6B1F-408D-8A84-E202E14B26FC Citation: Looney C, Smith DR, Collman SJ, Langor DW, Peterson MA (2016) Sawflies (Hymenoptera, Symphyta) newly recorded from Washington State. Journal of Hymenoptera Research 49: 129–159. doi: 10.3897/JHR.49.7104 Abstract Examination of museum specimens, unpublished collection data, and field surveys conducted between 2010 and 2014 resulted in records for 22 species of sawflies new to Washington State, seven of which are likely to be pest problems in ornamental landscapes. These data highlight the continued range expansion of exotic species across North America. These new records also indicate that our collective knowledge of Pacific Northwest arthropod biodiversity and biogeography is underdeveloped, even for a relatively well known and species-poor group of insects. -
Non-Native and Invasive Animals of Alaska: a Comprehensive List and Select Species Status Reports
NON-NATIVE AND INVASIVE ANIMALS OF ALASKA: A COMPREHENSIVE LIST AND SELECT SPECIES STATUS REPORTS FINAL REPORT Jodi McClory Tracey Gotthardt NON-NATIVE AND INVASIVE ANIMALS OF ALASKA: A COMPREHENSIVE LIST AND SELECT SPECIES STATUS REPORTS FINAL REPORT Jodi McClory and Tracey Gotthardt Alaska Natural Heritage Program Environment and Natural Resources Institute University of Alaska Anchorage 707 A Street, Anchorage AK 99501 January 2008 TABLE OF CONTENTS EXECUTIVE SUMMARY 4 INTRODUCTION 5 METHODOLOGY 5 RESULTS 6 DISCUSSION AND FUTURE DIRECTION 6 ACKNOWLEDGEMENTS 7 LITERATURE CITED 8 APPENDICES I: LIST OF NON-NATIVE ANIMAL SPECIES DOCUMENTED IN ALASKA 9 II: LIST OF NON-NATIVE ANIMAL SPECIES WITH THE POTENTIAL FOR INVASION IN ALASKA 17 III: STATUS REPORTS FOR SELECT NON-NATIVE ANIMAL SPECIES OF ALASKA 21 PACIFIC CHORUS FROG.......................................................................................................................... 22 RED-LEGGED FROG ................................................................................................................................24 ATLANTIC SALMON................................................................................................................................. 27 NORTHERN PIKE ..................................................................................................................................... 30 AMBER-MARKED BIRCH LEAFMINER .................................................................................................... 33 BIRCH LEAFMINER ................................................................................................................................