The Bees of Sub-Saharan Africa Will Lead to Better Documentation and Understanding of Bee Biodiversity in Africa
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Newsletter of the Biological Survey of Canada
Newsletter of the Biological Survey of Canada Vol. 40(1) Summer 2021 The Newsletter of the BSC is published twice a year by the In this issue Biological Survey of Canada, an incorporated not-for-profit From the editor’s desk............2 group devoted to promoting biodiversity science in Canada. Membership..........................3 President’s report...................4 BSC Facebook & Twitter...........5 Reminder: 2021 AGM Contributing to the BSC The Annual General Meeting will be held on June 23, 2021 Newsletter............................5 Reminder: 2021 AGM..............6 Request for specimens: ........6 Feature Articles: Student Corner 1. City Nature Challenge Bioblitz Shawn Abraham: New Student 2021-The view from 53.5 °N, Liaison for the BSC..........................7 by Greg Pohl......................14 Mayflies (mainlyHexagenia sp., Ephemeroptera: Ephemeridae): an 2. Arthropod Survey at Fort Ellice, MB important food source for adult by Robert E. Wrigley & colleagues walleye in NW Ontario lakes, by A. ................................................18 Ricker-Held & D.Beresford................8 Project Updates New book on Staphylinids published Student Corner by J. Klimaszewski & colleagues......11 New Student Liaison: Assessment of Chironomidae (Dip- Shawn Abraham .............................7 tera) of Far Northern Ontario by A. Namayandeh & D. Beresford.......11 Mayflies (mainlyHexagenia sp., Ephemerop- New Project tera: Ephemeridae): an important food source Help GloWorm document the distribu- for adult walleye in NW Ontario lakes, tion & status of native earthworms in by A. Ricker-Held & D.Beresford................8 Canada, by H.Proctor & colleagues...12 Feature Articles 1. City Nature Challenge Bioblitz Tales from the Field: Take me to the River, by Todd Lawton ............................26 2021-The view from 53.5 °N, by Greg Pohl..............................14 2. -
The Bees of Sub-Saharan Africa
A-PDF Split DEMO : Purchase from www.A-PDF.com to remove the watermark Genus Nasutapis Michener (Fig. 36E) Nasutapis has a distinct projection medioventrally on the clypeus. This genus is monotypic (Nasutapis straussorum Michener) and endemic to KwaZulu-Natal, South Africa, and found in nests of Braunsapis facialis (Gerstaecker). 8.6.2. Subfamily Nomadinae In sub-Saharan Africa the Nomadinae comprises four tribes and six genera. They are all cleptoparasitic. Diagnostic features for the subfamily are difficult to define, but almost each tribe has a distinctive feature, except Ammobatoidini. 8.6.2.1. Tribe Nomadini Genus Nomada Scopoli (Fig. 37A) Nomadini has one genus in sub-Saharan Africa, namely Nomada. There are ten species, occurring mostly in North-East and southern Africa. 8.6.2.2. Tribe Epeolini Genus Epeolus Latreille (Fig. 37B) Epeolini has one genus in sub-Saharan Africa, namely Epeolus. There are 13 species that occur mostly on the east side of the continent, along its entire length. 8.6.2.3. Tribe Ammobatoidini Genus Ammobatoides Radoszkowski (Fig. 37C) Ammobatoidini has one genus in sub-Saharan Africa, and it is known only from the holotype of Ammobatoides braunsi Bischoff. It was collected in Willowmore, South Africa. It therefore goes without saying that it is extremely rare. 8.6.2.4. Tribe Ammobatini The Ammobatini has four sub-Saharan genera. They all comprise cleptoparasitic bees. Ammobates has its centre of diversity in the Palaearctic, as does Chiasmognathus, which occurs just north of the Afrotropical Region and intrudes into sub-Saharan Africa. Pasites is mostly Afrotropical and Sphecodopsis is endemic to southern Africa. -
Hymenoptera: Colletidae): Emerging Patterns from the Southern End of the World Eduardo A
Journal of Biogeography (J. Biogeogr.) (2011) ORIGINAL Biogeography and diversification of ARTICLE colletid bees (Hymenoptera: Colletidae): emerging patterns from the southern end of the world Eduardo A. B. Almeida1,2*, Marcio R. Pie3, Sea´n G. Brady4 and Bryan N. Danforth2 1Departamento de Biologia, Faculdade de ABSTRACT Filosofia, Cieˆncias e Letras, Universidade de Aim The evolutionary history of bees is presumed to extend back in time to the Sa˜o Paulo, Ribeira˜o Preto, SP 14040-901, Brazil, 2Department of Entomology, Comstock Early Cretaceous. Among all major clades of bees, Colletidae has been a prime Hall, Cornell University, Ithaca, NY 14853, example of an ancient group whose Gondwanan origin probably precedes the USA, 3Departamento de Zoologia, complete break-up of Africa, Antarctica, Australia and South America, because Universidade Federal do Parana´, Curitiba, PR modern lineages of this family occur primarily in southern continents. In this paper, 81531-990, Brazil, 4Department of we aim to study the temporal and spatial diversification of colletid bees to better Entomology, National Museum of Natural understand the processes that have resulted in the present southern disjunctions. History, Smithsonian Institution, Washington, Location Southern continents. DC 20560, USA Methods We assembled a dataset comprising four nuclear genes of a broad sample of Colletidae. We used Bayesian inference analyses to estimate the phylogenetic tree topology and divergence times. Biogeographical relationships were investigated using event-based analytical methods: a Bayesian approach to dispersal–vicariance analysis, a likelihood-based dispersal–extinction– cladogenesis model and a Bayesian model. We also used lineage through time analyses to explore the tempo of radiations of Colletidae and their context in the biogeographical history of these bees. -
Keys for the Identification of Common Bees of Sri Lanka
28.2006 KeysJ.Natn.Sci.Foundation to the common bees Sri of Lanka Sri Lanka 2008 36 (1): 69-89 69 RESEARCH ARTICLE Keys for the identification of common bees of Sri Lanka W. A. Inoka P. Karunaratne and Jayanthi P. Edirisinghe* Department of Zoology, Faculty of Science,University of Peradeniya, Peradeniya Revised: 01 March 2007 ; Accepted: 15 February 2008 Abstract: Illustrated keys are provided for the identification A brief taxonomic history of 41 species of bees in 25 genera and three families that are commonly encountered on flowers of common flowering plants The earliest published work on bees of Sri Lanka dates of Sri Lanka. The generic and species keys to bees are annotated back to the British Colonial Period when Bingham2 with known natural history information on distribution, floral recorded, described and provided keys for 42 species hosts, special behaviour at flowers, nest type and nesting sites. of bees in 15 genera from Sri Lanka. Thereafter, the Details of external morphology of bees used in the keys have insect surveys conducted in Sri Lanka (1978-1998) by been included. A brief taxonomic history of bees relevant to the Smithsonian Institution, Washington resulted in the Sri Lanka is also included. identification of several bee species by Sakagami and Ebmer 3; Schwarz 4; Sakagami 5,6; Sakagami; Ebmer & Keywords: Common bees, floral hosts, identification-keys\, Tadauchi 7 , 8; Snelling 9 and Baker 10. These publications taxonomic features, Sri Lanka are noteworthy in that they include descriptions and species keys for specific genera. The landmark 11 INTRODUCTION publication on the bees of the world by Michener has included information and keys for several genera (27) of There has been a long felt need for a key for the bees documented from Sri Lanka. -
Bees of Sub-Saharan Africa Poster
Bees of Sub-Saharan Africa It is estimated that there are around 30 000 bee species worldwide of which about 20 500 have been described, 2755 occur in sub-Saharan Africa and about 1200 occur in South Africa. Bees, in many shapes and sizes, pollinate about 80% of all flowering plants and 75% of the vegetables, fruits and nuts we eat. The symbols next to each bee indicate their sociality, where they nest and where they get their food. Megachilidae are long tongued bees with two submarginal cells on their wings that collect pollen Apidae are long tongued bees with two or three submarginal wing cells that collect pollen on their hind legs. under their abdomens. The group comprises almost every type of nest building behaviour. Most are solitary but some are social. Parasitism includes social parasites, cleptoparasites and robbers. ♂ ♂ ♀ ♀ ♀ ♀ ♀ ♂ C ♀ C ♀ ♂ F Pasites ♀ appletoni C C F Cleft Cuckoo Ammobates ♀ Nomada gigas Bee auster Gnathanthidium Wasp Cuckoo Sandwalker prionognathum Bee Cuckoo Bee F Big Jawed Afromelecta fulvohirta Euaspis abdominalis Xylocopa lugubris Fidelia braunsiana Redtailed Cuckoo Bee Carder Bee Coelioxys circumscriptus Large Carpenter Bee Pathwork Cuckoo Bee Pot Bee Cone Cuckoo Bee ♀ ♂ ♀ ♀ ♂ C ♂ ♀ F ♂ C ♂ ♀ ♀ ♂ ♀ ♀ F ♀ ♂ F Ceratina Sphecodopsis Icteranthidium ♀ ♂ Schwarzia emmae moerenhouti Max Cuckoo Bee vespericena F grohmani Small Carpenter Bee Cape Cuckoo Ridge Cheeked Bee C F Hoplitis similis Carder Bee F Lithurgus spiniferus Big Resin Bee Aglaoapis trifasciata Stone Bee Toothed Cuckoo Bee F ♀ ♂ ♀ ♂ Aspidosmia arnoldi ♀ ♂ Ugly Faced Carder Bee ♀ F ♀ ♀ Thyreus pictus Xylocopa scioensis F F Neon Cuckoo Bee Afroheriades sp. ♀ Large Carpenter Bee Compsomelissa Macrogalea candida African Resin Bee Ochreriades F ♀ Stenoheriades sp. -
Novltatesamerican MUSEUM PUBLISHED by the AMERICAN MUSEUM of NATURAL HISTORY CENTRAL PARK WEST at 79TH STREET, NEW YORK, N.Y
NovltatesAMERICAN MUSEUM PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, N.Y. 10024 Number 3180, 39 pp., 17 figures, 8 tables August 23, 1996 Phylogenetic Analysis of the Cleptoparasitic Bees Belonging to the Nomadinae Based on Mature Larvae (Apoidea: Apidae) JEROME G. ROZEN, JR.' CONTENTS Abstract .................................................................... 2 Introduction .................................................................... 2 Acknowledgments .............................................................. 3 Historical Background ............................................................ 4 Methodology ...................................................................5 Evaluation of Characters ....................... .................................. 6 Monophyly of the Nomadinae ................ ................................... 10 Phylogeny of the Nomadinae ................ .................................... 12 Analysis 1. Based on larval features alone ...................................... 13 Analysis 2. Based on larval characters from current study and adult characters from Alexander (1990) ................. .................................... 13 Analysis 3. Based on larval characters from current study and adult characters from Roig-Alsina (1991) ................................................... 16 Analysis 4. Based on larval characters from current study and adult characters from Roig-Alsina and Michener (1993) ..................................... -
The Impact of Molecular Data on Our Understanding of Bee Phylogeny and Evolution
EN58CH04-Danforth ARI 5 December 2012 7:55 The Impact of Molecular Data on Our Understanding of Bee Phylogeny and Evolution Bryan N. Danforth,1∗ Sophie Cardinal,2 Christophe Praz,3 Eduardo A.B. Almeida,4 and Denis Michez5 1Department of Entomology, Cornell University, Ithaca, New York 14853; email: [email protected] 2Canadian National Collection of Insects, Agriculture Canada, Ottawa, Ontario K1A 0C6, Canada; email: [email protected] 3Institute of Biology, University of Neuchatel, Emile-Argand 11, 2009 Neuchatel, Switzerland; email: [email protected] 4Departamento de Biologia, FFCLRP-Universidade de Sao˜ Paulo, 14040-901 Ribeirao˜ Preto, Sao˜ Paulo, Brazil; email: [email protected] 5University of Mons, Laboratory of Zoology, 7000 Mons, Belgium; email: [email protected] Annu. Rev. Entomol. 2013. 58:57–78 Keywords First published online as a Review in Advance on Hymenoptera, Apoidea, bees, molecular systematics, sociality, parasitism, August 28, 2012 plant-insect interactions The Annual Review of Entomology is online at ento.annualreviews.org Abstract by 77.56.160.109 on 01/14/13. For personal use only. This article’s doi: Our understanding of bee phylogeny has improved over the past fifteen years 10.1146/annurev-ento-120811-153633 as a result of new data, primarily nucleotide sequence data, and new methods, Copyright c 2013 by Annual Reviews. primarily model-based methods of phylogeny reconstruction. Phylogenetic All rights reserved Annu. Rev. Entomol. 2013.58:57-78. Downloaded from www.annualreviews.org studies based on single or, more commonly, multilocus data sets have helped ∗ Corresponding author resolve the placement of bees within the superfamily Apoidea; the relation- ships among the seven families of bees; and the relationships among bee subfamilies, tribes, genera, and species. -
Phylogeny and Classification of the Parasitic Bee Tribe Epeolini (Hymenoptera: Apidae, Nomadinae)^
Ac Scientific Papers Natural History Museum The University of Kansas 06 October 2004 Number 33:1-51 Phylogeny and classification of the parasitic bee tribe Epeolini (Hymenoptera: Apidae, Nomadinae)^ By Molly G. Rightmyer y\CZ Division of E)itoiiiologi/, Nntuinl History Museiiui mid Biodizvrsity Rcsenrch Center, jV^Ar^^ and Eiitomology Progrniii, Department of Ecology nnd Evolutionary Biology, The Unii>ersity of Kansas, Lawrence, Kansas, 66045-7523 CONTENTS ^AB'"^^?Sy ABSTRACT 2 lJHIVE^^^ ' INTRODUCTION 2 Acknowledgments 2 HISTORICAL REVIEW 3 METHODS AND MATERIALS 5 MORPHOLOGY 7 PsEUDOPYGiDiAL Area 7 Sting Apparatus 7 Male Internal Sclerites 11 PHYLOGENETIC RESULTS 11 SYSTEMATICS 13 Tribe Epeolini Robertson 13 Subtribe Odyneropsina Handlirsch new status 14 Genus Odyneropsis Schrottky 14 Subgenus Odyneropsis Schrottky new status 15 Subgenus Parammobates Friese new status 15 Rhogepeolina new subtribe 15 Genus Rhogepeolus Moure 15 Rhogepeolina + (Epeolina + Thalestriina) 16 Epeolina + Thalestriina 16 Subtribe Epeolina Robertson new status 16 Genus Epeolus Latreille 16 'Contribution No. 3397 of the Division of Entomology, Natural History Museum and Biodiversity Research Center, University of Kansas. Natural ISSN No. 1094-0782 © History Museum, The University of Kansas _ . «i„,, I <*»ro»V Ernst K'ayr Li^^rary Zoology Museum of Comparawe Harvard University Ac Scientific Papers Natural History Museum The University of Kansas 06 October 2004 NumLx-r 33:1-51 Phylogeny and classification of the parasitic bee tribe Epeolini (Hymenoptera: Apidae, Nomadinae)' -
Seasonal Patterns in the Diversity of Apis and Non-Apis Bees in an Agro-Ecosystem: a Case Study from Eastern Dry Zone of Karnataka
Current Biotica 6(4): 432-444, 2013 ISSN 0973-4031 Seasonal patterns in the diversity of Apis and non-Apis bees in an agro-ecosystem: A case study from eastern dry zone of Karnataka Arati Pannure* and K. Chandrashekara Department of Entomology, University of Agricultural Sciences, Gandhi Krishi Vigyan Kendra, Bangalore - 560065, India *E-mail: [email protected] ABSTRACT A study has been taken up to investigate seasonal patterns in the diversity of bee fauna in different landscape elements of GKVK farming system, Bangalore. The study was carried out over a period of one year from August, 2009 to October, 2010. During sampling, a total of 2030 bees were collected which belong to 20 genera and 65 species. In this paper, the temporal variation in abundance of bee species is examined and compared the patterns in different species. The study concluded that there was a trend towards increased bee abundance and richness during winter with increased flowering with a subsequent decline over the course of the summer season. The assessment of diversity of any taxon at a given temporal or spatial scale is important for its conservation and management. KEY WORDS: Agroecosystem, Apis, Halictids, Megachilids, Non-Apis bees INTRODUCTION (Heemert et al., 1990; Tuell et al., 2009). Moreover, their populations and Apoidea has an important role as diversity also serve as bioindicators of pollinating agents in the ecosystem. the state of many environments Among the pollinator groups, honey (Tscharntke et al., 1998; Keven, 1999; bees have been considered a priority Steffan-Dewenter et al., 2002; group. In addition to honey bees, non- Tylianakis et al., 2004). -
Floral Guilds of Bees in Sagebrush Steppe: Comparing Bee Usage Of
ABSTRACT: Healthy plant communities of the American sagebrush steppe consist of mostly wind-polli- • nated shrubs and grasses interspersed with a diverse mix of mostly spring-blooming, herbaceous perennial wildflowers. Native, nonsocial bees are their common floral visitors, but their floral associations and abundances are poorly known. Extrapolating from the few available pollination studies, bees are the primary pollinators needed for seed production. Bees, therefore, will underpin the success of ambitious seeding efforts to restore native forbs to impoverished sagebrush steppe communities following vast Floral Guilds of wildfires. This study quantitatively characterized the floral guilds of 17 prevalent wildflower species of the Great Basin that are, or could be, available for restoration seed mixes. More than 3800 bees repre- senting >170 species were sampled from >35,000 plants. Species of Osmia, Andrena, Bombus, Eucera, Bees in Sagebrush Halictus, and Lasioglossum bees prevailed. The most thoroughly collected floral guilds, at Balsamorhiza sagittata and Astragalus filipes, comprised 76 and 85 native bee species, respectively. Pollen-specialists Steppe: Comparing dominated guilds at Lomatium dissectum, Penstemon speciosus, and several congenerics. In contrast, the two native wildflowers used most often in sagebrush steppe seeding mixes—Achillea millefolium and Linum lewisii—attracted the fewest bees, most of them unimportant in the other floral guilds. Suc- Bee Usage of cessfully seeding more of the other wildflowers studied here would greatly improve degraded sagebrush Wildflowers steppe for its diverse native bee communities. Index terms: Apoidea, Asteraceae, Great Basin, oligolecty, restoration Available for Postfire INTRODUCTION twice a decade (Whisenant 1990). Massive Restoration wildfires are burning record acreages of the The American sagebrush steppe grows American West; two fires in 2007 together across the basins and foothills over much burned >500,000 ha of shrub-steppe and 1,3 James H. -
Bntomojauna ZEITSCHRIFT FÜR ENTOMOLOGIE
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Entomofauna Jahr/Year: 1982 Band/Volume: 0003 Autor(en)/Author(s): Warncke Klaus Artikel/Article: Zur Systematik der Bienen - Die Unterfamilie Nomadinae (Hymenoptera, Apidae). 97-126 © Entomofauna Ansfelden/Austria; download unter www.biologiezentrum.at Bntomojauna ZEITSCHRIFT FÜR ENTOMOLOGIE Band 3, Heft 8 ISSN 02.50-4413 Linz, 30.April 1982 Zur Systematik der Bienen - Die Unterfamilie Nomadinae (Hymenoptera, Apidae) Klaus Warncke Abstract 1. The Status of the parasitic bees within the system of the bees / Apidae was examined. Because of their turn- rounded 3. Metatarsi the Nomadinae derived from the base of the Dasypodinae and not as till now from the Melitti- nae (= Melitta KIRBY, 1802, Macropis PANZER,1809, Antho- phoridae). 2. For Palaearctic only 5 genera will be recognized: Am- mobatoides RADOSZKOWSKI,1867, Biastes PANZER,1806, Epeo- lus LATREILLE, 1802, and Pasites JURINE, 1807. Acantho- nomada SCHWARZ, 1966, is önly a subgenus of Nomada SCO- POLI, 1770, Schmiedeknechtia FRIESE, 1896, of Ammobatoi- des RADOSZKOWSKI, 1867, Ammobat.es LATREILLE, 1809, and the like of Pasites JURINE, 1807, Triepeolus ROBERTSON, 1901,..and Oxybiast.es MAVROMOUSTAKIS, 1954, of Epeolus LA- TREILLE, 1802. 3- New synonyms are: Holcopasites ASHMEAD, 1899, and Schmiedeknechtia FRIESE, 1896, subg. Cyrtopasites MAVRO- 97 © Entomofauna Ansfelden/Austria; download unter www.biologiezentrum.at MOUSTAKIS, 1963, - Ammobatoides RADOSZKOWSKI,1867, subg. Schmiedeknechtia FRIESE, 1896, Neopasites ASHMEAD, I89S, and Neopasites ASHMEAD,1898, subg. Micropasites LINSLEY, 1942, = Biastes PANZER, 1806, Morgania SMITH, 1854, --• Pa- sites JURINE, 1807, Trophocleptria HOLMBERG, 1886, and Rhinepeolus MOURE, 1955, = Epeolus LATREILLE, 1802, Doe- ringiella HOLMBERG,1884, = Epeolus LATREILLE,1802, subg. -
Scope: Munis Entomology & Zoology Publishes a Wide Variety of Papers
Munis Entomology & Zoology Mun. Ent. Zool. https://www.munisentzool.org/ (January, 2021) 457 ISSN 1306-3022 © MRG ___________________________________________________________ EXPLORING THE ACULEATA HYMENOPTERA OF BANGLADESH BY DNA BARCODING OF MALAISE TRAP COLLECTION Santosh Mazumdar*, Paul D. N. Hebert** and Badrul Amin Bhuiya*** * Department of Zoology, University of Chittagong, BANGLADESH. E-mail: [email protected]; ORCID ID: 0000-0001-6403-577X ** Centre for Biodiversity Genomics, University of Guelph, 50 Stone Road East, Guelph, Ontario, CANADA. ORCID ID: 0000-0002-3081-6700 *** Biodiversity Research for Environment & Ecosystem Protection (BREEP), Chattogram- 4325, BANGLADESH. [Mazumdar, S., Hebert, P. D. N. & Bhuiya, B. A. 2021. Exploring the Aculeata Hymenoptera of Bangladesh by DNA barcoding of Malaise trap collection. Munis Entomology & Zoology, 16 (1): 457-464] ABSTRACT: Aculeata hymenopterans play a crucial role in ecology and economics. Diversity analysis of 901 Aculeata wasps at Chittagong University Campus a site in Bangladesh was performed by sequencing DNA barcodes (658 bp sequence from the 5′-end of cytochromeoxidase I). Specimens were collected by a Malaise trap from April 2014 to March 2015. The results revealed 22 species and 42 genera from 20 families in three superfamilies namely Apoidea, Chrysidoidea and Vespoidea. Among them 15 species, 22 genera, two subfamilies (Dolichoderinae and Ponerinae), and one family named Dryinidae are the first county records in Bangladesh. All the specimen records, with the Barcode Index Numbers (BINs) are available on the Barcode of Life Data System (BOLD). KEY WORDS: Aculeata Hymenoptera, Malaise trap, DNA barcode, Bangladesh Aculeata hymenopterans or stinging wasps (Hymenoptera: Aculeata) such as bees, ants, and many wasps play vital ecological roles as predators and pollinators and some have medicinal value as well (Zimmermann & Vilhelmsen, 2016).