Halictidae This Family Comprises Two Genera, Halictus and Lasioglossum, Which Can Be Tricky to Separate

Total Page:16

File Type:pdf, Size:1020Kb

Halictidae This Family Comprises Two Genera, Halictus and Lasioglossum, Which Can Be Tricky to Separate Halictidae This family comprises two genera, Halictus and Lasioglossum, which can be tricky to separate. All Halictidae have a groove, looking rather like a hair parting at the tip of the abdomen, called a rima. Most species have bands on the abdomen. In Halictus these are on the hind margin, but in Lasioglossum they are at the front of each tergite, often partly covered by the hind edge of the preceding tergite. Some females have orange legs and many of the males have pale leg markings with some also having a pale patch on the lower clypeus. Some species have a metallic greenish cuticle. The tongue is short and pollen is collected on the hind legs. Some members of the genus are eusocial, having larger egg-laying females (queens) and smaller sterile females (workers) which help at the nest. Nesting occurs in the ground, sometimes in aggregations. Only (mated) females survive the winter, with both sexes hatching from the first spring brood. The genus is parasitised by various Sphecodes bees. Halictus confusus This species is very similar to H. tumulorum: please refer to that species for a description. Flight times Recorded in May – September. Distribution Recorded at Roydon Common (MEA) and in the Brecks, with five post-2000 records, three still to be confirmed(GN, TS). Halictus confusus 4 3 2 1 0 9 2000 – 2014 8 1980 – 1999 Pre 1980 5 6 7 8 9 0 1 2 3 4 5 Habitat Sandy grassland, sometimes with Heather. Flowers visited No information Nesting No information Parasites None known (BWARS). Halictus rubicundus Females This bee could be mistaken for an Andrena but for the presence of a rima and the lack of facial foveae. The head and thorax hair is red and there are white marginal bands on the abdomen, interrupted centrally in T1 and T2. The cuticle and hair of the hind tibiae and the mid and hind tarsi is orange. Males are similar but slimmer with long antennae. The tibiae and tarsi of all legs are largely yellow and there is yellow mark on the clypeus. The labrum is also yellow. Flight times April – August with males recorded from July. Halictus rubicundus female at nest hole. Spalla Gap, Weybourne 20th May 2010 Distribution Widespread in the Brecks and the east of the county. Halictus rubicundus 4 3 2 1 0 9 8 2000 – 2014 1980 – 1999 Pre 1980 5 6 7 8 9 0 1 2 3 4 5 Halictus rubicundus male. Wharfedale, Yorkshire 16th August 2010 Habitat Heathland and other habitats with gravelly soils, including Broadland (Hickling). Flowers visited Bramble, Dandelion, Oxford Ragwort, White Bryony. Nesting Nesting aggregation on low cliff at Spalla Gap, Weybourne. A eusocial species (BWARS). Parasites Sphecodes gibbus and S. monilicornis (BWARS). Halictus tumulorum Parasites Sphecodes ephippius (SF). Females This species is much smaller than the last and rather broad bodied. The cuticle has a dull greenish sheen, though this can be hard to see in some individuals. The tergites have dull white hind margins and also flattened hairs at the anterior tergite edges. Females of H. confusus are almost identical but have broader white margins to the tergites which do not narrow centrally (SF). Males are also metallic green. The antennae are very long and the tibia, tarsus and most of the femur of all legs are bright yellow. The mandibles, labrum and tip of the clypeus are also yellow. Males can be separated from H. confusus Halictus tumulorum female. Holkham 8th males only from details of genitalia. September 2014 Flight times April – October, with males recorded from June. Distribution Widespread and common. Halictus tumulorum 4 3 2 1 0 9 2000 – 2014 8 1980 – 1999 Pre 1980 5 6 7 8 9 0 1 2 3 4 5 th Halictus tumulorum male. Pandy, Wales 26 Habitat Woodland, heathland, churchyards, September 2015 gardens, quarries, river valleys. Flowers visited Bramble, Cinquefoil, Fleabane, Germander Speedwell, Sedum, Mullein, Ragwort, Scabious, White Bryony. Males are sometimes seen in clusters in one flower. Nesting Nests in aggregations. Eusocial: small females are likely to be sterile workers. No county information. .
Loading...
Loading...
Loading...
Loading...

—— Preview end. ——

Recommended publications
  • Bischoff & Partner
    Wasserstraßen-Neubauamt Aschaffenburg Ausbau der Bundeswasserstraße Main in den Stauhaltungen Ottendorf und Knetzgau Vegetationskundliche und faunistische Untersuchungen Heft 3.5: Faunistische Untersuchungen Bienen und Wespen Weitere Hefte: Heft 1: Biotoptypenkartierung Heft 2: Pflanzensoziologische Kartierung und Einschätzung der Beeinträchtigung der Vegetation Bearbeiter: Dr. Reinhard Patrzich Dipl.-Biol. Armin Six Inh.: Dr. U. Wendt und Dipl.-Ing. J. Rössler Landschaftsökologie und Projektplanung 55442 Stromberg – Staatsstr. 1 Tel.: 06724/1329 – Fax: 06724/939593 Projekt-Nr.: 2609 eMail: info@bischoff-u-partner.de September 2009 INHALT I 1 EINFÜHRUNG .................................................................................................................... 1 2 METHODIK ......................................................................................................................... 2 3 ERGEBNISSE ..................................................................................................................... 3 3.1 Nachgewiesene Arten ................................................................................................... 3 3.2 Ökologie und Vorkommen der nachgewiesenen Bienen und Wespen .......................... 4 3.2.1 Chrysiidae ............................................................................................................. 4 3.2.2 Pompilidae ............................................................................................................. 4 3.2.3 Mutillidae ..............................................................................................................
    [Show full text]
  • Comparative Methods Offer Powerful Insights Into Social Evolution in Bees Sarah Kocher, Robert Paxton
    Comparative methods offer powerful insights into social evolution in bees Sarah Kocher, Robert Paxton To cite this version: Sarah Kocher, Robert Paxton. Comparative methods offer powerful insights into social evolution in bees. Apidologie, Springer Verlag, 2014, 45 (3), pp.289-305. 10.1007/s13592-014-0268-3. hal- 01234748 HAL Id: hal-01234748 https://hal.archives-ouvertes.fr/hal-01234748 Submitted on 27 Nov 2015 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. Apidologie (2014) 45:289–305 Review article * INRA, DIB and Springer-Verlag France, 2014 DOI: 10.1007/s13592-014-0268-3 Comparative methods offer powerful insights into social evolution in bees 1 2 Sarah D. KOCHER , Robert J. PAXTON 1Department of Organismic and Evolutionary Biology, Museum of Comparative Zoology, Harvard University, Cambridge, MA, USA 2Institute for Biology, Martin-Luther-University Halle-Wittenberg, Halle, Germany Received 9 September 2013 – Revised 8 December 2013 – Accepted 2 January 2014 Abstract – Bees are excellent models for studying the evolution of sociality. While most species are solitary, many form social groups. The most complex form of social behavior, eusociality, has arisen independently four times within the bees.
    [Show full text]
  • Journal of Melittology Bee Biology, Ecology, Evolution, & Systematics the Latest Buzz in Bee Biology No
    Journal of Melittology Bee Biology, Ecology, Evolution, & Systematics The latest buzz in bee biology No. 13, pp. 1–11 26 July 2013 A new species, Lasioglossum (Eickwortia) hienae, from Mexico (Apoidea: Halictidae) Jason Gibbs1 & Sheila Dumesh2 Abstract. A new species from Colima, Mexico, Lasioglossum (Eickwortia) hienae Gibbs & Du- mesh, new species, is described and illustrated. Lasioglossum hienae is distinguished from re- lated species based on a combination of morphological, geographical, and molecular evidence. A species distribution model is used to predict the potential distribution of the known species of L. (Eickwortia). An identification key is provided. INTRODUCTION The bee genus Lasioglossum Curtis (1833) is exceptionally diverse in terms of species richness, habitat use, and social behavior (Michener, 1974, 1979, 2000, 2007; Yanega, 1997; Schwarz et al., 2007). Eickwortia McGinley, 1999, now recognized as a subgenus of Lasioglossum (Michener 2000, 2007), was proposed for two species of high- elevation bees in Mexico and Central America, Lasioglossum nyctere (Vachal, 1904) and L. alexanderi (McGinley, 1999). Lasioglossum (Eickwortia) belongs to the informal group known as the Hemihalictus series, which is recognizable by its weak distal wing vena- tion (Michener, 2007). Ascher & Pickering (2013) have included these two species in L. (Evylaeus) Robertson, a subgenus we treat in a much narrower sense (Gibbs et al., 2013). The taxonomic limits of Lasioglossum subgenera require revision (Gibbs et al., 2012b, 2013), but recognition of the subgenus L. (Eickwortia) seems reasonable based on its apomorphic traits, including infuscate wings, strongly bidentate mandibles of the females, and slender metasoma of the males. We are reluctant to describe new species based on few specimens, but in the case of rare bees like L.
    [Show full text]
  • Molecular Ecology and Social Evolution of the Eastern Carpenter Bee
    Molecular ecology and social evolution of the eastern carpenter bee, Xylocopa virginica Jessica L. Vickruck, B.Sc., M.Sc. Department of Biological Sciences Submitted in partial fulfillment of the requirements for the degree of PhD Faculty of Mathematics and Science, Brock University St. Catharines, Ontario © 2017 Abstract Bees are extremely valuable models in both ecology and evolutionary biology. Their link to agriculture and sensitivity to climate change make them an excellent group to examine how anthropogenic disturbance can affect how genes flow through populations. In addition, many bees demonstrate behavioural flexibility, making certain species excellent models with which to study the evolution of social groups. This thesis studies the molecular ecology and social evolution of one such bee, the eastern carpenter bee, Xylocopa virginica. As a generalist native pollinator that nests almost exclusively in milled lumber, anthropogenic disturbance and climate change have the power to drastically alter how genes flow through eastern carpenter bee populations. In addition, X. virginica is facultatively social and is an excellent organism to examine how species evolve from solitary to group living. Across their range of eastern North America, X. virginica appears to be structured into three main subpopulations: a northern group, a western group and a core group. Population genetic analyses suggest that the northern and potentially the western group represent recent range expansions. Climate data also suggest that summer and winter temperatures describe a significant amount of the genetic differentiation seen across their range. Taken together, this suggests that climate warming may have allowed eastern carpenter bees to expand their range northward. Despite nesting predominantly in disturbed areas, eastern carpenter bees have adapted to newly available habitat and appear to be thriving.
    [Show full text]
  • Notes on Alien and Native Bees (Hymenoptera: Apoidea) from the Hawaiian Islands1
    Records of the Hawaii Biological Survey for 2012. Edited by Neal L. Evenhuis & Lucius G. Eldredge. Bishop Museum Occasional Papers 114: 61 –65 (2013) Notes on alien and native bees (Hymenoptera : Apoidea ) from the Hawaiian Islands 1 KARl N. M AGNACCA 2,3 Hawai‘i Division of Forestry and Wildlife, c/o University of Hawai‘i–Hilo, Dept. of Biology, 200 W. Kawili St., Hilo, Hawaii 96720, USA; email: knm956@gmail.com JASoN GiBBS Cornell University, Department of Entomology, 3119 Comstock Hall, Ithaca, New York, 14853, USA; email: jason.gibbs@cornell.edu SAM dRoeGe U.S. Geological Survey, Patuxent Wildlife Research Center, 11510 American Holly Drive, Laurel, Maryland 20708-4017, USA; email: sdroege@usgs.gov) Four introduced bees are recorded from the Hawaiian islands for the first time, along with notes on previously recorded species, including rediscovery of the endemic Hylaeus anom - alus (Perkins, 1899). Both of the new Lasioglossum species are relatively recent arrivals, but their precise date of introduction is not known because the alien Lasioglossum are often ignored by collectors and are poorly represented in collections. it had been assumed that all were L. impavidum (Sandhouse, 1924), which has been present in the islands since at least 1957 (Beardsley 1958, Beardsley 1959). A recent survey of o‘ahu lowland disturbed sites by Sd found three distinct species – L. impavidum , L. imbrex Gibbs, 2010, and L. microlepoides (ellis, 1914) – prompting a review of earlier specimens. Unless otherwise noted, specimens listed below were collected by KNM; specimens are deposited at the Bishop Museum (BPBM) and University of Hawai‘i–Mānoa insect Museum (UHiM).
    [Show full text]
  • Profile for Halictus Harmonius
    Packer, L. 2005. Species Profile: Halictus harmonius. In Shepherd, M. D., D. M. Vaughan, and S. H. Black (Eds). Red List of Pollinator Insects of North America. CD-ROM Version 1 (May 2005). Portland, OR: The Xerces Society for Invertebrate Conservation. ________________________________________________________________________ Halictus harmonius Sandhouse, 1941 (Halictidae: Halictinae: Halictini) ________________________________________________________________________ Prepared by Dr. Laurence Packer, York University. ________________________________________________________________________ SUMMARY Halictus harmonius is a rare localized species that has only ever been recorded from the foothills of the San Bernardino and, but with less certainty, from the San Jacinto mountains in Southern California. This whole area is subject to considerable anthropogenic disturbance through construction, pollution and agriculture. The species is active for long periods in spring and summer and appears to be primitively eusocial with macrocephalic queens and smaller workers. It appears not to be restricted in pollen and nectar source plants. A survey of suitable habitat in the small area from which the species is known is badly required. CONSERVATION STATUS Xerces Red List Status: Critically Imperiled Other Rankings: Canada – Species at Risk Act: N/A Canada – provincial status: N/A Mexico: N/A USA – Endangered Species Act None USA – state status: None Nature Serve: N/A IUICH Red List: N/A ________________________________________________________________________ SPECIES PROFILE DESCRIPTION Halictus harmonius is a member of the subgenus Seladonia. This is the only subgenus of Halictine bee in North America that has the combination of greenish metallic coloration and apical bands of pale hairs on the metasomal terga. Halictine bees can be readily identified on the basis of the strongly curved basal vein and, except in certain cleptoparasitic forms, by the pseudopygidial area on female T5.
    [Show full text]
  • Hymenoptera: Aculeata Part 1 – Bees
    SCOTTISH INVERTEBRATE SPECIES KNOWLEDGE DOSSIER Hymenoptera: Aculeata Part 1 – Bees A. NUMBER OF SPECIES IN UK: 318 B. NUMBER OF SPECIES IN SCOTLAND: 110 (4 thought to be extinct, 2 may be found – insufficient data) C. EXPERT CONTACTS Please contact scotland@buglife.org.uk for details. D. SPECIES OF CONSERVATION CONCERN Listed species UK Biodiversity Action Plan Species known to occur in Scotland (the current list was published in August 2007): Andrena tarsata Tormentil mining bee Bombus distinguendus Great yellow bumblebee Bombus muscorum Moss (Large) carder bumblebee Bombus ruderarius Red-shanked (Red-tailed) carder bumblebee Colletes floralis Northern colletes Osmia inermis a mason bee Osmia parietina a mason bee Osmia uncinata a mason bee Bombus distinguendus is also listed under the Species Action Framework of Scottish Natural Heritage, launched in 2007 (Category 1: Species for Conservation Action). 1 Other species The Scottish Biodiversity List was published in 2005 and lists the additional species (arranged below by sub-family): Andreninae Andrena cineraria Andrena helvola Andrena marginata Andrena nitida 1 Andrena ruficrus Anthophorinae Anthidium maniculatum Anthophora furcata Epeolus variegatus Nomada fabriciana Nomada leucophthalma Nomada obtusifrons Nomada robertjeotiana Sphecodes gibbus Apinae Bombus monticola Colletinae Colletes daviesanus Colletes fodiens Hylaeus brevicornis Halictinae Lasioglossum fulvicorne Lasioglossum smeathmanellum Lasioglossum villosulum Megachillinae Osmia aurulenta Osmia caruelescens Osmia rufa Stelis
    [Show full text]
  • Phylogeny of the Bee Genus Halictus (Hymenoptera: Halictidae) Based on Parsimony and Likelihood Analyses of Nuclear EF-1A Sequen
    Molecular Phylogenetics and Evolution Vol. 13, No. 3, December, pp. 605–618, 1999 Article ID mpev.1999.0670, available online at http://www.idealibrary.com on Phylogeny of the Bee Genus Halictus (Hymenoptera: Halictidae) Based on Parsimony and Likelihood Analyses of Nuclear EF-1␣ Sequence Data Bryan N. Danforth,* Herve´ Sauquet,† and Laurence Packer‡ *Department of Entomology, Cornell University, Comstock Hall, Ithaca, New York 14853-0901; †c/o Dr. A. Le Thomas, E.P.H.E., Laboratoire de Biologie et Evolution des Plantes vasculaires, Museum National d’Histoire, Naturelle, 16, rue Buffon, 75005 Paris, France; and ‡Department of Biology and Faculty of Environmental Studies, York University, 4700 Keele Street, Toronto, Ontario, M3J 1P3, Canada Received December 23, 1998; revised April 8, 1999 INTRODUCTION We investigated higher-level phylogenetic relation- ships within the genus Halictus based on parsimony Halictid bees (Halictidae) are model organisms for and maximum likelihood (ML) analysis of elongation studying the evolution of social behavior in insects. Of factor-1␣ DNA sequence data. Our data set includes 41 all the bees, this family includes the greatest number of OTUs representing 35 species of halictine bees from a eusocial species and shows the greatest intra- and diverse sample of outgroup genera and from the three interspecific variability in social behavior (Michener, widely recognized subgenera of Halictus (Halictus s.s., 1974). Within the halictid subfamily Halictinae there Seladonia, and Vestitohalictus). We analyzed 1513 total are seven genera and subgenera that include all or aligned nucleotide sites spanning three exons and two some eusocial species: Halictus (Halictus), Halictus introns. Equal-weights parsimony analysis of the over- (Seladonia), Lasioglossum (Evylaeus), Lasioglossum all data set yielded 144 equally parsimonious trees.
    [Show full text]
  • Lasioglossum Sexstrigatum (Hymenoptera: Apidae, Halictinae) New to Britain
    90 BR. J. ENT. NAT. HIST., 24: 2011 LASIOGLOSSUM SEXSTRIGATUM (HYMENOPTERA: APIDAE, HALICTINAE) NEW TO BRITAIN ROGER D. HAWKINS 30D, Meadowcroft Close, Horley, Surrey RH6 9EL ABSTRACT A female Lasioglossum sexstrigatum (Schenck), a species not previously known in Britain, was found in a sandpit near Merstham in Surrey in June 2008. Despite several searches, no further specimens of this bee have been recorded from this site. Recent evidence shows this species is widely distributed in central mainland Europe. INTRODUCTION AND DISCOVERY Small black bees, particularly those in the genus Lasioglossum, form a difficult area of study for the student of aculeate Hymenoptera, but can be identified with some confidence by careful use of a key and with reference to a reliably named collection. One such insect, a female bee taken at a flooded sandpit near Merstham in east Surrey, caused particular difficulty. This bee was small (6mm long) and black, the angles of the propodeum were rounded, and the marginal area of tergite 1 was shining, almost smooth, and without punctures. The specimen had one very distinctive feature: there was a narrow band of dense white hairs towards each side of the apical margin of each of tergites 2 to 4 (Plate 7, Fig. 2). The bee was given several different provisional names before being identified conclusively as Lasioglossum sexstrigatum (Schenck), a European species not previously recorded in Britain. The site is owned by WBB Minerals, part of the Sibelco Group, and since 2002 has been managed as a nature reserve by the Surrey Wildlife Trust under the name of Spynes Mere.
    [Show full text]
  • Ancestral Monogamy Shows Kin Selection Is Key to the Evolution Of
    REPORTS Fig. 3. Comparison of 15. E. A. Gladyshev, I. R. Arkhipova, Proc. Natl. Acad. Sci. bdelloid telomeric/TE-rich U.S.A. 104, 9352 (2007). 16. D. B. Mark Welch, J. L. Mark Welch, M. Meselson, regions (A) with bdelloid Proc. Natl. Acad. Sci. U.S.A. 105, 5145 (2008). gene-rich regions (B) 17. J. H. Hur, thesis, Harvard University (2006). and with other model 18. N. N. Pouchkina-Stantcheva, A. Tunnacliffe, Mol. Biol. invertebrates (C). Pie Evol. 22, 1482 (2005). charts were built with 19. See supporting material on Science Online. 921,903 base pairs (bp) 20. D. M. Baird, J. Rowson, D. Wynford-Thomas, D. Kipling, Nat. Genet. 33, 203 (2003). (A) and 661,316 bp (B) 21. R. Finking, M. A. Marahiel, Annu. Rev. Microbiol. 58, 453 of genomic DNA, respec- (2004). tively (excluding one of 22. D. Mark Welch, M. Meselson, Science 288, 1211 the two colinear part- (2000). ners). For TE count, ~1.3 23. N. Kondo, N. Nikoh, N. Ijichi, M. Shimada, T. Fukatsu, Mb of genomic DNA in Proc. Natl. Acad. Sci. U.S.A. 99, 14280 (2002). 24. K. Suga, D. Mark Welch, Y. Tanaka, Y. Sakakura, each data set was ana- A. Hagiwara, PLoS ONE 2, e671 (2007). lyzed (including both 25. A. Haviv-Chesner, Y. Kobayashi, A. Gabriel, M. Kupiec, colinear partners). The Nucleic Acids Res. 35, 5192 (2007). size of each sector cor- 26. T. de Lange, Genes Dev. 19, 2100 (2005). responds to the percent- 27. R. Jain, M. C. Rivera, J. A. Lake, Proc. Natl.
    [Show full text]
  • Searles Mazzacano Pollinators - September 12, 2016 Who Pollinates? Who Pollinates?
    Understanding and sustaining Insect Pollinators insect pollinators in your garden A. Importance of pollinators B. Cast of characters C. Creating habitat Mining bee; CASM Celeste A. Searles Mazzacano, Ph.D. D. Sustaining habitat Presented for EMSWCD E. Projects & resources Flower scarab; CASM © 2016 C. A. Searles Mazzacano yellow-faced bumble bee; C.A.S. Mazzacano 1 2 Why are pollinators important? Why are pollinators important? • pollination: transfer of pollen • 70% of flowering plants within or between flowers for pollinated by insects fertilization, seed & fruit set • ~1,000 plants grown • wind, insects, birds, mammals worldwide for food, fibers, drinks, spices, & medicine honey bee; C.A.S. Mazzacano pollinated by animals Bat Conservation International • most pollinated by bees Importance of bees to food production Bumble bee on echinacea; (Wilson & Carrill, 2016) Wikimedia Commons 3 4 Searles Mazzacano_Pollinators - September 12, 2016 Who pollinates? Who pollinates? More than bees!!!!! sand wasp; C.A.S. Mazzacano More than insects!!!!! • Wasps • Bats • Flies Tayler/naturepl.com • Hummingbirds • Beetles • Moths & butterflies Bee fly; C.A.S. Mazzacano C.A.S. Mazzacano 5 6 Who pollinates? Who pollinates? summer leafcutter bee, Bumble bee; C.A.S. Mazzacano “Managed” bees are Crown Bees catalog Much more than economically important European honey bees!!!!! • honey bees, bumble bees, - native bees (> 4000 NA spp.) orchard mason bees, alfalfa leafcutter bees ‣ social: bumble bees ‣ solitary: mining, mason, leafcutter, orchard, sweat, digger, and carpenter bees Sweat bee; C.A.S. Mazzacano CA almond grove; Kathy Keatley Garvey 7 8 Searles Mazzacano_Pollinators - September 12, 2016 Challenges for pollinators Challenges for pollinators Many stressors • Colony Collapse Disorder (2006) in managed honey • habitat loss bee hives • pesticides fouldbrood-infected larvae; Univ.
    [Show full text]
  • Observations on the Nests of Costa Rican Halictus with Taxonomic Notes on N Eotropical Species (Hymenoptera: Halictidae)
    Rev. BioI. Trop., 18(1, 2): 11-31, 1971 Observations on the nests of Costa Rican Halictus with taxonomic notes on N eotropical species (Hymenoptera: Halictidae) by Alvaro Wille* and Charles D. Michener** (Received for publication July 4, 1969) This paper consists of descriptions of nests of the two species oE Costa Rican burrowing bees of the genus HalictrlS (subgenus Seladonia), H. hesperus and H. lutescens, together with taxonomic observations on the three neotropical species of the subgenus. The observations on H. hesperus were mostly made from Febmary 25 to March 20, 1954. Data on H. lutescens were gathered from Jnne 23 to 26, 1963. Division of labor between the anthors was as follows: one of us (A. W.) was involved in all the field work. The other was involved in the field work oE 1963 and is responsible for the taxonomic section and the preparation of the manuscript. NESTS AND LIFE CYCLE SEASONAL CYCLE: All observations were made in the lowland parts of the province oE Guanacaste, Costa Rica. This is a relatively arid savanna reglOn with dry gallery forest along the streams. The dry season is from mid-Decem­ ber to May. In February and March, 1954, H. hesper!ls was found to be extremely active provisioning cells. The nests contained young oE all ages. Local in­ habitants reported an extreme abundance of bees (probably males) flying over * Facultad de Agronomfa, 'Universidad de Costa Rica, Ciu.!ad Universitaria, Cos­ ta Rica. ** Departments of Entomology and of Systematics and Ecology, The University of Kansas. Lawrence. Kansas 66044, U.S.A.
    [Show full text]