Macropis Cuckoo Bee (Epeoloides Pilosulus) in Canada
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Wisconsin Bee Identification Guide
WisconsinWisconsin BeeBee IdentificationIdentification GuideGuide Developed by Patrick Liesch, Christy Stewart, and Christine Wen Honey Bee (Apis mellifera) The honey bee is perhaps our best-known pollinator. Honey bees are not native to North America and were brought over with early settlers. Honey bees are mid-sized bees (~ ½ inch long) and have brownish bodies with bands of pale hairs on the abdomen. Honey bees are unique with their social behavior, living together year-round as a colony consisting of thousands of individuals. Honey bees forage on a wide variety of plants and their colonies can be useful in agricultural settings for their pollination services. Honey bees are our only bee that produces honey, which they use as a food source for the colony during the winter months. In many cases, the honey bees you encounter may be from a local beekeeper’s hive. Occasionally, wild honey bee colonies can become established in cavities in hollow trees and similar settings. Photo by Christy Stewart Bumble bees (Bombus sp.) Bumble bees are some of our most recognizable bees. They are amongst our largest bees and can be close to 1 inch long, although many species are between ½ inch and ¾ inch long. There are ~20 species of bumble bees in Wisconsin and most have a robust, fuzzy appearance. Bumble bees tend to be very hairy and have black bodies with patches of yellow or orange depending on the species. Bumble bees are a type of social bee Bombus rufocinctus and live in small colonies consisting of dozens to a few hundred workers. Photo by Christy Stewart Their nests tend to be constructed in preexisting underground cavities, such as former chipmunk or rabbit burrows. -
Seasonal and Spatial Patterns of Mortality and Sex Ratio in the Alfalfa
Seasonal and spatial patterns of mortality and sex ratio in the alfalfa leafcutting bee, Megachile rotundata (F.) by Ruth Pettinga ONeil A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology Montana State University © Copyright by Ruth Pettinga ONeil (2004) Abstract: Nests from five seed alfalfa sites of the alfalfa leafcutting bee Megachile rotundata (F.) were monitored over the duration of the nesting season in 2000 and 2001, from early July through late August. Cells containing progeny of known age and known position within the nest were subsequently analyzed for five commonly encountered categories of pre-diapause mortality in this species. Chalkbrood and pollen ball had the strongest seasonal relationships of mortality factors studied. Chalkbrood incidence was highest in early-produced cells. Pollen ball was higher in late-season cells. Chalkbrood, parasitism by the chalcid Pteromalus venustus, and death of older larvae and prepupae , due to unknown source(s) exhibited the strongest cell-position relationships. Both chalkbrood and parasitoid incidence were highest in the inner portions of nests. The “unknown” category of mortality was highest in outer portions of nests. Sex ratio was determined for a subset of progeny reared to adulthood. The ratio of females to males is highest in cells in inner nest positions. Sex ratio is female-biased very early in the nesting season, when all cells being provisioned are the inner cells of nests, due to the strong positional effect on sex ratio. SEASONAL AND SPATIAL PATTERNS OF MORTALITY AND SEX RATIO IN THE ALFALFA LEAFCUTTING BEE, Megachile rotundata (F.) by . -
Redalyc.CLEPTOPARASITE BEES, with EMPHASIS on THE
Acta Biológica Colombiana ISSN: 0120-548X [email protected] Universidad Nacional de Colombia Sede Bogotá Colombia ALVES-DOS-SANTOS, ISABEL CLEPTOPARASITE BEES, WITH EMPHASIS ON THE OILBEES HOSTS Acta Biológica Colombiana, vol. 14, núm. 2, 2009, pp. 107-113 Universidad Nacional de Colombia Sede Bogotá Bogotá, Colombia Available in: http://www.redalyc.org/articulo.oa?id=319027883009 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Acta biol. Colomb., Vol. 14 No. 2, 2009 107 - 114 CLEPTOPARASITE BEES, WITH EMPHASIS ON THE OILBEES HOSTS Abejas cleptoparásitas, con énfasis en las abejas hospederas coletoras de aceite ISABEL ALVES-DOS-SANTOS1, Ph. D. 1Departamento de Ecologia, IBUSP. Universidade de São Paulo, Rua do Matão 321, trav 14. São Paulo 05508-900 Brazil. [email protected] Presentado 1 de noviembre de 2008, aceptado 1 de febrero de 2009, correcciones 7 de julio de 2009. ABSTRACT Cleptoparasite bees lay their eggs inside nests constructed by other bee species and the larvae feed on pollen provided by the host, in this case, solitary bees. The cleptoparasite (adult and larvae) show many morphological and behavior adaptations to this life style. In this paper I present some data on the cleptoparasite bees whose hosts are bees specialized to collect floral oil. Key words: solitary bee, interspecific interaction, parasitic strategies, hospicidal larvae. RESUMEN Las abejas Cleptoparásitas depositan sus huevos en nidos construídos por otras especies de abejas y las larvas se alimentan del polen que proveen las hospederas, en este caso, abejas solitarias. -
Creating a Pollinator Garden for Native Specialist Bees of New York and the Northeast
Creating a pollinator garden for native specialist bees of New York and the Northeast Maria van Dyke Kristine Boys Rosemarie Parker Robert Wesley Bryan Danforth From Cover Photo: Additional species not readily visible in photo - Baptisia australis, Cornus sp., Heuchera americana, Monarda didyma, Phlox carolina, Solidago nemoralis, Solidago sempervirens, Symphyotrichum pilosum var. pringlii. These shade-loving species are in a nearby bed. Acknowledgements This project was supported by the NYS Natural Heritage Program under the NYS Pollinator Protection Plan and Environmental Protection Fund. In addition, we offer our appreciation to Jarrod Fowler for his research into compiling lists of specialist bees and their host plants in the eastern United States. Creating a Pollinator Garden for Specialist Bees in New York Table of Contents Introduction _________________________________________________________________________ 1 Native bees and plants _________________________________________________________________ 3 Nesting Resources ____________________________________________________________________ 3 Planning your garden __________________________________________________________________ 4 Site assessment and planning: ____________________________________________________ 5 Site preparation: _______________________________________________________________ 5 Design: _______________________________________________________________________ 6 Soil: _________________________________________________________________________ 6 Sun Exposure: _________________________________________________________________ -
Bees and Wasps of the East Sussex South Downs
A SURVEY OF THE BEES AND WASPS OF FIFTEEN CHALK GRASSLAND AND CHALK HEATH SITES WITHIN THE EAST SUSSEX SOUTH DOWNS Steven Falk, 2011 A SURVEY OF THE BEES AND WASPS OF FIFTEEN CHALK GRASSLAND AND CHALK HEATH SITES WITHIN THE EAST SUSSEX SOUTH DOWNS Steven Falk, 2011 Abstract For six years between 2003 and 2008, over 100 site visits were made to fifteen chalk grassland and chalk heath sites within the South Downs of Vice-county 14 (East Sussex). This produced a list of 227 bee and wasp species and revealed the comparative frequency of different species, the comparative richness of different sites and provided a basic insight into how many of the species interact with the South Downs at a site and landscape level. The study revealed that, in addition to the character of the semi-natural grasslands present, the bee and wasp fauna is also influenced by the more intensively-managed agricultural landscapes of the Downs, with many species taking advantage of blossoming hedge shrubs, flowery fallow fields, flowery arable field margins, flowering crops such as Rape, plus plants such as buttercups, thistles and dandelions within relatively improved pasture. Some very rare species were encountered, notably the bee Halictus eurygnathus Blüthgen which had not been seen in Britain since 1946. This was eventually recorded at seven sites and was associated with an abundance of Greater Knapweed. The very rare bees Anthophora retusa (Linnaeus) and Andrena niveata Friese were also observed foraging on several dates during their flight periods, providing a better insight into their ecology and conservation requirements. -
Nova Scotia Highlands
Selecting Plants for Pollinators A Guide for Gardeners, Farmers, and Land Managers In the Nova Scotia Highlands Sydney Glace Bay Antigonish Table of CONTENTS Why Support Pollinators? 4 Getting Started 5 Nova Scotia Highlands 6 Meet the Pollinators 8 Plant Traits 10 Developing Plantings 12 Farms 13 Public Lands 14 Home Landscapes 15 Plants That Attract Pollinators 16 Habitat hints 20 Habitat and Nesting requirements 21 This is one of several guides for S.H.A.R.E. 22 different regions of North America. We welcome your feedback to assist us in making the future guides Checklist 22 useful. Please contact us at [email protected] Resources and Feedback 23 2 Selecting Plants for Pollinators Selecting Plants for Pollinators A Guide for Gardeners, Farmers, and Land Managers In the Nova Scotia Highlands Sydney Glace Bay Antigonish A NAPPC and Pollinator Partnership Canada™ Publication Nova Scotia Highlands 3 Why support pollinators? IN THEIR 1996 BOOK, THE FORGOttEN POLLINATORS, Buchmann and Nabhan estimated that animal pollinators are needed for the reproduction “Flowering plants of 90% of flowering plants and one third of human food crops. Each of us depends on these industrious pollinators in a practical way to provide us across wild, with the wide range of foods we eat. In addition, pollinators are part of the intricate web that supports the biological diversity in natural ecosystems that helps sustain our quality of life. farmed and even Abundant and healthy populations of pollinators can improve fruit set and quality, and increase fruit size. In farming situations this increases urban landscapes production per hectare. -
Fauna Helvetica 9. Apidae 4
Eur. J. Entomol. 105: 163, 2008 http://www.eje.cz/scripts/viewabstract.php?abstract=1317 ISSN 1210-5759 (print), 1802-8829 (online) BOOK REVIEW AMIET F., HERRMANN M., MÜLLER A. & NEUMEYER R.: FAUNA figures of some characters, taxonomic classification of species HELVETICA 9. APIDAE 4 (Anthidum, Chelostoma, and commentary on the individual species (description of Coelioxys, Dioxys, Heriades, Lithurgus, Megachile, Osmia & females and males, distribution of each species with a map of Stelis). Centre suisse de cartographie de la faune (CSCF), the records for Switzerland, flight period, cleptoparasites or host Neuchâtel, 2004, 272 pp., 249 figs, 117 distrib. maps. ISSN and additional notices). The records are graphically presented as 1422-6367. Hb: ISBN 2-88414-021-2. Price CHF 45.00. recent or old (before 1970). In the 5th volume, the recent records are further categorised as before of after 1990. At the end of AMIET F., HERRMANN M., MÜLLER A. & NEUMEYER R.: FAUNA each book there are references and a species index. HELVETICA 20. APIDAE 5 (Ammobates, Ammobatoides, The keys are well constructed. They are suitable for identifi- Anthophora, Biastes, Ceratina, Dasypoda, Epeoloides, Epeolus, cation by beginners. The identification keys are constructed as a Eucera, Macropis, Melecta, Melitta, Nomada, Pasites, Tetralo- sensu lato; for example, the Osmia key includes species of seve- nia, Thyreus, Xylocopa). Centre suisse de cartographie de la ral other supraspecific taxons (Hoplosmia, Hoplitis, Metalli- faune (CSCF), Neuchâtel, 2007, 356 pp., 423 figs, 142 distrib. nella, Neosmia, Protosmia, Erythrosmia and Tergosmia). I maps. ISSN 1422-6367. Hb: ISBN 978-2-88414-032-4. Price prefer identification keys that branch according to supraspecific CHF 50.00. -
Bees, Wasps & Ants
Sheringham and Beeston Regis Commons SSSI / SAC FAUNA: Hymenoptera INSECTA (Pterygota) Family/Order English Name. Scientific Name. Authority. Grid Ref. Tetrad/ Last Km sq. Common. Record. HYMENOPTERA. PAMPHILIDAE: Sawfly. Pamphilius inanitus (Villers, 1789) TG1642 1987? (Bees, Wasps and Ants) ARGIDAE: Elm Zig-zag Sawfly. Aproceros leucopoda Takeuchi, 1939 TG1642 14R/B 2020 Bramble Sawfly. Arge cyaneocrocea (Forster, 1771) TG1642 2016 Sawfly. Arge gracilicornis (Klug, 1814 ) TG1642 1987? CIMBICIDAE: Honeysuckle Sawfly. Abia lonicerae (Linnaeus) TG1641 14Q/B 2015 Club-horned Sawfly. Abia sericera (Linnaeus) TG1642 14R/B 2014 Club-horned Sawfly. Zaraea fasciata Linnaeus, 1758 TG1641/42 14R,14Q/B 2014 Birch Sawfly. Cimbex femoratus (Linnaeus, 1758) TG1642 14R/B 2017 SIRICIDAE: Greater Horntail Wasp. Urocerus gigas (Linnaeus, 1758) TG1642 14R/S 1992 CEPHIDAE: Sawfly. Calameuta pallipes (Klug, 1803) TG1642 1987? TENTHREDINIDAE: Willow Sawfly. Pontania proxima (Lepeletier, 1823) TG1642 14R/BS 2009 Willow Sawfly. Eupontania pedunculi (Hartig, 1837) TG1642 14R/B 1999 Willow Sawfly. Eupontainia viminalis (Linnaeus, 1758) TG1642 14R/B 2002 Willow Sawfly. Pontainia bridgemanii (Cameron, 1883) TG1642 14R/B 1999 Sawfly. Caliroa annulipes (Klug, 1816) TG1642 14R/S 2002 Hazel Sawfly. Craesus septentrionalis (Linnaeus, 1758) TG1641 14Q/B 2017 Sawfly. Blennocampa phyllocolpa Viitasaari & Vikberg, 1985 TG1642/41 14R,14Q/B 2003 Sawfly. Selandria serva (Fabricius, 1793) TG1642 14R/B 2013 Sawfly. Aneugmenus padi (Linnaeus, 1761) TG1642 1987? Bracken Sawfly. Strongylogaster multifasciata (Geoffroy, 1785) TG1642 14R/BS 2020 Sawfly. Dichrodolerus vestigialis (Klug, 1818) TG1642 1996 Sawfly. Dolerus germanicus (Fabricius, 1775) TG1642 1987? Sawfly. Eutomostethus ephippium (Panzer, 1798) TG1642 14R/BS 2020 Sawfly. Poodolerus aeneus Hartig, 1837 TG1642 1987? Sawfly. Dolerus brevitarus Hartig TG1642 1987? Sawfly. -
The Evolution of Parasitism Among Bees
Utah State University DigitalCommons@USU All PIRU Publications Pollinating Insects Research Unit 1970 The Evolution of Parasitism Among Bees George E. Bohart Utah State University Follow this and additional works at: https://digitalcommons.usu.edu/piru_pubs Part of the Entomology Commons Recommended Citation Bohart, George E. 1970. The evolution and parasitism among bees. Faculty Honor Lecture, Utah State University, April 22, 1970. 41st 30 p. This Presentation is brought to you for free and open access by the Pollinating Insects Research Unit at DigitalCommons@USU. It has been accepted for inclusion in All PIRU Publications by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. 41st FACULTY HONOR LECTURE - APRIL• 22, 1970 than State Un/ve/S/ty THE EVOLUTION OF PARASITISM AMONG BEES George E. Bohart Entomology Research Division, Agricultural Research Service, United States Department of Agriculture FORTY -FIRST HONOR LECTURE SPRING 1970 THE FACUL TV ASSOCIATION FORTY-FIRST ANNUAL HONOR LECTURE DELIVERED AT THE UNIVERSITY A basic ob jective of The Faculty As ociation of tah State University, in the words of its con titution. is: to encourage intellectual growth and development of its mem bers by pon oring and arranging for the publication of two an nual facult_ research lectures in the fi elds of ( I ) the biological and exact cience , including engi neering. called the Annual Faculty Honor Lecture in the Natural Sciences; and (2) the humanities and ocial ciences. incl uding education and busi ness administration, called the Annual Faculty Honor Lecture in the Humanities. The administration of the University i ympatheric wi th the e aims and shares, through the Scholarly Publications Committee, the costs of publishing and distributing the e lectures. -
Pollinators in Peril: a Systematic Status Review of North American
POLLINATORS in Peril A systematic status review of North American and Hawaiian native bees Kelsey Kopec & Lori Ann Burd • Center for Biological Diversity • February 2017 Executive Summary hile the decline of European honeybees in the United States and beyond has been well publicized in recent years, the more than 4,000 species of native bees in North W America and Hawaii have been much less documented. Although these native bees are not as well known as honeybees, they play a vital role in functioning ecosystems and also provide more than $3 billion dollars in fruit-pollination services each year just in the United States. For this first-of-its-kind analysis, the Center for Biological Diversity conducted a systematic review of the status of all 4,337 North American and Hawaiian native bees. Our key findings: • Among native bee species with sufficient data to assess (1,437), more than half (749) are declining. • Nearly 1 in 4 (347 native bee species) is imperiled and at increasing risk of extinction. • For many of the bee species lacking sufficient population data, it’s likely they are also declining or at risk of extinction. Additional research is urgently needed to protect them. • A primary driver of these declines is agricultural intensification, which includes habitat destruction and pesticide use. Other major threats are climate change and urbanization. These troubling findings come as a growing body of research has revealed that more than 40 percent of insect pollinators globally are highly threatened, including many of the native bees critical to unprompted crop and wildflower pollination across the United States. -
Land Uses That Support Wild Bee (Hymenoptera: Apoidea: Anthophila) Communities Within an Agricultural Matrix
Land uses that support wild bee (Hymenoptera: Apoidea: Anthophila) communities within an agricultural matrix A DISSERTATION SUBMITTED TO THE FACULTY OF THE GRADUATE SCHOOL OF THE UNIVERSITY OF MINNESOTA BY Elaine Celeste Evans IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY Dr. Marla Spivak December 2016 © Elaine Evans 2016 Acknowledgements Many people helped me successfully complete this project. Many years ago, my advisor, mentor, hero, and friend, Marla Spivak, saw potential in me and helped me to become an effective scientist and educator working to create a more bee-friendly world. I have benefitted immensely from her guidance and support. The Bee Lab team, both those that helped me directly in the field, and those that advised along the way through analysis and writing, have provided a dreamy workplace: Joel Gardner, Matt Smart, Renata Borba, Katie Lee, Gary Reuter, Becky Masterman, Judy Wu, Ian Lane, Morgan Carr- Markell. My committee helped guide me along the way and steer me in the right direction: Dan Cariveau (gold star for much advice on analysis), Diane Larson, Ralph Holzenthal, and Karen Oberauser. Cooperation with Chip Eullis and Jordan Neau at the USGS enabled detailed land use analysis. The bee taxonomists who helped me with bee identification were essential for the success of this project: Jason Gibbs, John Ascher, Sam Droege, Mike Arduser, and Karen Wright. My friends and family eased my burden with their enthusiasm for me to follow my passion and their understanding of my monomania. My husband Paul Metzger and my son August supported me in uncountable ways. -
PETITION to LIST the VARIABLE CUCKOO BUMBLE BEE Bombus Variabilis (Cresson 1872) UNDER the ENDANGERED SPECIES ACT and CONCURRENTLY DESIGNATE CRITICAL HABITAT
BEFORE THE SECRETARY OF THE INTERIOR PETITION TO LIST THE VARIABLE CUCKOO BUMBLE BEE Bombus variabilis (Cresson 1872) UNDER THE ENDANGERED SPECIES ACT AND CONCURRENTLY DESIGNATE CRITICAL HABITAT Variable Cuckoo Bumble Bee (top) male side (bottom) male face USGS Bee Inventory and Monitoring Lab Photo by Brook Goggins CENTER FOR BIOLOGICAL DIVERSITY April 27th, 2021 NOTICE OF PETITION Charles Wooley, Regional Director Deb Haaland, Secretary Region 3 U.S. Fish and Wildlife Service U.S. Department of the Interior 5600 American Blvd. West, Suite 990 1849 C Street NW Bloomington, MN 55437-1458 Washington, D.C. 20240 [email protected] [email protected] Leopoldo Miranda, Regional Director Martha Williams, Principal Deputy Director Region 4 U.S. Fish and Wildlife Service U.S. Fish and Wildlife Service 1875 Century Blvd. NE 1849 C Street NW Atlanta, GA 30345 Washington, D.C. 20240 [email protected] [email protected] Gary Frazer, Assistant Director for Wendi Weber, Regional Director Endangered Species Region 5 U.S. Fish and Wildlife Service U.S. Fish and Wildlife Service 300 Westgate Center Dr. 1840 C Street NW Hadley, MA 01035 Washington, D.C. 20240 [email protected] [email protected] Noreen Walsh, Regional Director Amy Leuders, Regional Director Region 6 U.S. Fish and Wildlife Service Region 2 U.S. Fish and Wildlife Service 134 Union Boulevard, Suite 650 P.O. Box 1306 Lakewood, CO 80228 Albuquerque, NM 87103-1306 [email protected] [email protected] ii Pursuant to Section 4(b) of the Endangered Species Act (“ESA”), 16 U.S.C. § 1533(b); Section 553(e) of the Administrative Procedure Act, 5 U.S.C.