Information Sheet Native Bees
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5.4 Insect Visitors to Marianthus Aquilonaris and Surrounding Flora
REPORT: Insect visitors to Marianthus aquilonaris and surrounding flora Nov 2-4, 2019 Kit Prendergast, Native bee scientist BSc First Class Honours, PhD researcher and Forrest Scholar On behalf of Botanica Consulting 1 REPORT: Insect visitors to Marianthus aquilonaris and surrounding flora Nov 2-4 2019 Kit Prendergast, Native bee scientist Background Marianthus aquilonaris (Fig. 1) was declared as Rare Flora under the Western Australian Wildlife Conservation Act 1950 in 2002 under the name Marianthus sp. Bremer, and is ranked as Critically Endangered (CR) under the International Union for Conservation of Nature (IUCN 2001) criteria B1ab(iii,v)+2ab(iii,v); C2a(ii) due to its extent of occurrence being less than 100 km2, its area of occupancy being less than 10 km2, a continuing decline in the area, extent and/or quality of its habitat and number of mature individuals and there being less than 250 mature individuals known at the time of ranking (Appendix A). However, it no longer meets these criteria as more plants have been found, and a recommendation has been proposed to be made by DBCA to the Threatened Species Scientific Committee (TSSC) to change its conservation status to CR B1ab(iii,v)+2ab(iii,v) (Appendix A), but this recommendation has not gone ahead (DEC, 2010). Despite its listing as CR under the Western Australian Biodiversity Conservation Act 2016, the species is not currently listed under the Environment Protection and Biodiversity Conservation Act 1999. The main threats to the species are mining/exploration, track maintenance and inappropriate fire regimes (DEC, 2010). Fig. 1. Marianthus aquilonaris, showing flower, buds and leaves. -
A Second Contribution to the Biology of Ctenocolletes Bees (Hymenoptera: Apoidea: Stenotritidae)
Rec. West. AU8t. Mus. 1987. 13(2): 189-201 A second contribution to the biology of Ctenocolletes bees (Hymenoptera: Apoidea: Stenotritidae) Terry F. Houston* Abstract Field observations of adult behaviour (particularly foraging and mating) and nests of five species of Ctenocolletes are presented and compared with earlier obser vations. All studied species are solitary and ground-nesting. Nests are unusual in lacking tumuli and those of C. albomarginatus and C. nicholsoni are remarkably deep (2.7-3.2 m). C. fulvescens is unusual in the genus in having a summer/autumn (rather than a winter/spring) flight season and in exhibiting matinal foraging in females and a bimodal flight pattern in males. Conjugate flight of mating pairs and territorial hovering and darting flights of males are recorded for additional ,species. Meloidae (Coleoptera) are confirmed as cleptoparasites in nests of C. nicholsoni and a Crassifoenus species (Hymen optera: Gasteruptiidae) is recorded from nests or nesting areas of four Ctenocolletes species. Introduction In a previous paper (Houston 1984), I recorded the first details of the bionomics of bees in the genus Ctenocolletes. Nests of only one species (C. ordensis Michener) were described and much of the information on adult behaviour was fragmentary, providing only a very incomplete picture of the bionomics of the genus as a whole. The observations presented here were made opportunistically during field work at various Western Australian localities in 1983-1985 and are similarly fragmentary. Nevertheless, they augment and significantly extend earlier ob servations. Examination of the nests of several species has revealed some sig nificant interspecific differences and discovery of the nests of C. -
Barrett, M., S. Schneider, P. Sachdeva, A. Gomez, S. Buchmann
Journal of Comparative Physiology A https://doi.org/10.1007/s00359-021-01492-4 ORIGINAL PAPER Neuroanatomical diferentiation associated with alternative reproductive tactics in male arid land bees, Centris pallida and Amegilla dawsoni Meghan Barrett1 · Sophi Schneider2 · Purnima Sachdeva1 · Angelina Gomez1 · Stephen Buchmann3,4 · Sean O’Donnell1,5 Received: 1 February 2021 / Revised: 19 May 2021 / Accepted: 22 May 2021 © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 Abstract Alternative reproductive tactics (ARTs) occur when there is categorical variation in the reproductive strategies of a sex within a population. These diferent behavioral phenotypes can expose animals to distinct cognitive challenges, which may be addressed through neuroanatomical diferentiation. The dramatic phenotypic plasticity underlying ARTs provides a powerful opportunity to study how intraspecifc nervous system variation can support distinct cognitive abilities. We hypothesized that conspecifc animals pursuing ARTs would exhibit dissimilar brain architecture. Dimorphic males of the bee species Centris pallida and Amegilla dawsoni use alternative mate location strategies that rely primarily on either olfaction (large-morph) or vision (small-morph) to fnd females. This variation in behavior led us to predict increased volumes of the brain regions supporting their primarily chemosensory or visual mate location strategies. Large-morph males relying mainly on olfaction had relatively larger antennal lobes and relatively smaller optic lobes than small-morph males relying primarily on visual cues. In both species, as relative volumes of the optic lobe increased, the relative volume of the antennal lobe decreased. In addition, A. dawsoni large males had relatively larger mushroom body lips, which process olfactory inputs. -
Managing Alternative Pollinators a Handbook for Beekeepers, Growers, and Conservationists
Managing Alternative Pollinators A Handbook for Beekeepers, Growers, and Conservationists ERIC MADER • MARLA SPIVAK • ELAINE EVANS Fair Use of this PDF file of Managing Alternative Pollinators: A Handbook for Beekeepers, Growers, and Conservationists, SARE Handbook 11, NRAES-186 By Eric Mader, Marla Spivak, and Elaine Evans Co-published by SARE and NRAES, February 2010 You can print copies of the PDF pages for personal use. If a complete copy is needed, we encourage you to purchase a copy as described below. Pages can be printed and copied for educational use. The book, authors, SARE, and NRAES should be acknowledged. Here is a sample acknowledgement: ----From Managing Alternative Pollinators: A Handbook for Beekeepers, Growers, and Conservationists, SARE Handbook 11, by Eric Mader, Marla Spivak, and Elaine Evans, and co- published by SARE and NRAES.---- No use of the PDF should diminish the marketability of the printed version. If you have questions about fair use of this PDF, contact NRAES. Purchasing the Book You can purchase printed copies on NRAES secure web site, www.nraes.org, or by calling (607) 255-7654. The book can also be purchased from SARE, visit www.sare.org. The list price is $23.50 plus shipping and handling. Quantity discounts are available. SARE and NRAES discount schedules differ. NRAES PO Box 4557 Ithaca, NY 14852-4557 Phone: (607) 255-7654 Fax: (607) 254-8770 Email: [email protected] Web: www.nraes.org SARE 1122 Patapsco Building University of Maryland College Park, MD 20742-6715 (301) 405-8020 (301) 405-7711 – Fax www.sare.org More information on SARE and NRAES is included at the end of this PDF. -
Hylaeus Strenuus (Hymenoptera: Colletidae), a New Alien Bee on O'ahu
Records of the Hawaii Biological Survey for 2009 –2010. Edited by Neal L. Evenhuis & Lucius G. Eldredge. Bishop Museum Occasional Papers 109: 23 –24 (2011) Hylaeus strenuus (Hymenoptera : Colletidae) , a new alien bee on O‘ahu kARl N. M AGNACCA (University of Hawai‘i Hilo, Department of Biology, 200 W. kawili Street, Hilo, Hawaii 96720, USA; email: [email protected] ), WAlTeR T. N AGAMiNe (Plant Pest Control Branch, Hawaii Department of Agriculture, 1428 S. king Street, Honolulu, Hawai‘i 96814, USA; email: [email protected] ) & HOlGeR H. D ATHe (Senckenberg Deutsches entomologisches institut, eberswalder Straße 90, 15374 Müncheberg, Germany; email: [email protected] ) Hymenoptera : Colletidae Hylaeus strenuus (Cameron) New state record The first specimens of this species, one male and two females, were collected at Magic island, Ala Moana Beach Park, in early 2007 by Patrick Aldrich. These were sent to Roy Snelling at the los Angeles County Museum and tentatively identified as a member of the African subgenus Deranchylaeus . Unfortunately, with Mr. Snelling’s sudden passing last year, the specimens were lost, and with no additional ones available, it was uncertain whether the species was established. Recently, WTN rediscovered this species at several sites along the southeast coast between Ala Moana Beach Park and koko Crater, in company with the introduced car - penter bee Ceratina smaragdula . Reevaluation of it by one of us (HHD) identified it as Hylaeus strenuus (Cameron, 1897), which is described from Barrackpore, West Bengal, india. virtually nothing is known about it in its home range, possibly due in part to the poor original description—the type is a male, not a female as described, and does not match the text very well. -
Food Load Manipulation Ability Shapes Flight Morphology in Females Of
Polidori et al. Frontiers in Zoology 2013, 10:36 http://www.frontiersinzoology.com/content/10/1/36 RESEARCH Open Access Food load manipulation ability shapes flight morphology in females of central-place foraging Hymenoptera Carlo Polidori1*, Angelica Crottini2, Lidia Della Venezia3,5, Jesús Selfa4, Nicola Saino5 and Diego Rubolini5 Abstract Background: Ecological constraints related to foraging are expected to affect the evolution of morphological traits relevant to food capture, manipulation and transport. Females of central-place foraging Hymenoptera vary in their food load manipulation ability. Bees and social wasps modulate the amount of food taken per foraging trip (in terms of e.g. number of pollen grains or parts of prey), while solitary wasps carry exclusively entire prey items. We hypothesized that the foraging constraints acting on females of the latter species, imposed by the upper limit to the load size they are able to transport in flight, should promote the evolution of a greater load-lifting capacity and manoeuvrability, specifically in terms of greater flight muscle to body mass ratio and lower wing loading. Results: Our comparative study of 28 species confirms that, accounting for shared ancestry, female flight muscle ratio was significantly higher and wing loading lower in species taking entire prey compared to those that are able to modulate load size. Body mass had no effect on flight muscle ratio, though it strongly and negatively co-varied with wing loading. Across species, flight muscle ratio and wing loading were negatively correlated, suggesting coevolution of these traits. Conclusions: Natural selection has led to the coevolution of resource load manipulation ability and morphological traits affecting flying ability with additional loads in females of central-place foraging Hymenoptera. -
Intro Outline
THE REPRODUCTIVE ECOLOGY OF TWO TERRESTRIAL ORCHIDS, CALADENIA RIGIDA AND CALADENIA TENTACULATA RENATE FAAST Submitted for the degree of Doctor of Philosophy School of Earth and Environmental Sciences The University of Adelaide, South Australia December, 2009 i . DEcLARATION This work contains no material which has been accepted for the award of any other degree or diploma in any university or other tertiary institution to Renate Faast and, to the best of my knowledge and belief, contains no material previously published or written by another person, except where due reference has been made in the text. I give consent to this copy of my thesis when deposited in the University Library, being made available for loan and photocopying, subject to the provisions of the Copyright Act 1968. The author acknowledges that copyright of published works contained within this thesis (as listed below) resides with the copyright holder(s) of those works. I also give permission for the digital version of my thesis to be made available on the web, via the University's digital research repository, the Library catalogue, the Australasian Digital Theses Program (ADTP) and also through web search engines. Published works contained within this thesis: Faast R, Farrington L, Facelli JM, Austin AD (2009) Bees and white spiders: unravelling the pollination' syndrome of C aladenia ri gída (Orchidaceae). Australian Joumal of Botany 57:315-325. Faast R, Facelli JM (2009) Grazrngorchids: impact of florivory on two species of Calademz (Orchidaceae). Australian Journal of Botany 57:361-372. Farrington L, Macgillivray P, Faast R, Austin AD (2009) Evaluating molecular tools for Calad,enia (Orchidaceae) species identification. -
BÖCEKLERİN SINIFLANDIRILMASI (Takım Düzeyinde)
BÖCEKLERİN SINIFLANDIRILMASI (TAKIM DÜZEYİNDE) GÖKHAN AYDIN 2016 Editör : Gökhan AYDIN Dizgi : Ziya ÖNCÜ ISBN : 978-605-87432-3-6 Böceklerin Sınıflandırılması isimli eğitim amaçlı hazırlanan bilgisayar programı için lütfen aşağıda verilen linki tıklayarak programı ücretsiz olarak bilgisayarınıza yükleyin. http://atabeymyo.sdu.edu.tr/assets/uploads/sites/76/files/siniflama-05102016.exe Eğitim Amaçlı Bilgisayar Programı ISBN: 978-605-87432-2-9 İçindekiler İçindekiler i Önsöz vi 1. Protura - Coneheads 1 1.1 Özellikleri 1 1.2 Ekonomik Önemi 2 1.3 Bunları Biliyor musunuz? 2 2. Collembola - Springtails 3 2.1 Özellikleri 3 2.2 Ekonomik Önemi 4 2.3 Bunları Biliyor musunuz? 4 3. Thysanura - Silverfish 6 3.1 Özellikleri 6 3.2 Ekonomik Önemi 7 3.3 Bunları Biliyor musunuz? 7 4. Microcoryphia - Bristletails 8 4.1 Özellikleri 8 4.2 Ekonomik Önemi 9 5. Diplura 10 5.1 Özellikleri 10 5.2 Ekonomik Önemi 10 5.3 Bunları Biliyor musunuz? 11 6. Plocoptera – Stoneflies 12 6.1 Özellikleri 12 6.2 Ekonomik Önemi 12 6.3 Bunları Biliyor musunuz? 13 7. Embioptera - webspinners 14 7.1 Özellikleri 15 7.2 Ekonomik Önemi 15 7.3 Bunları Biliyor musunuz? 15 8. Orthoptera–Grasshoppers, Crickets 16 8.1 Özellikleri 16 8.2 Ekonomik Önemi 16 8.3 Bunları Biliyor musunuz? 17 i 9. Phasmida - Walkingsticks 20 9.1 Özellikleri 20 9.2 Ekonomik Önemi 21 9.3 Bunları Biliyor musunuz? 21 10. Dermaptera - Earwigs 23 10.1 Özellikleri 23 10.2 Ekonomik Önemi 24 10.3 Bunları Biliyor musunuz? 24 11. Zoraptera 25 11.1 Özellikleri 25 11.2 Ekonomik Önemi 25 11.3 Bunları Biliyor musunuz? 26 12. -
1. Padil Species Factsheet Scientific Name: Common Name Image
1. PaDIL Species Factsheet Scientific Name: Homalictus (Homalictus) houstoni Walker, 1986 (Hymenoptera: Halictidae: Halictinae: Halictini) Common Name Native houstoni halictid bee Live link: http://www.padil.gov.au/pollinators/Pest/Main/138367 Image Library Australian Pollinators Live link: http://www.padil.gov.au/pollinators/ Partners for Australian Pollinators image library Western Australian Museum https://museum.wa.gov.au/ South Australian Museum https://www.samuseum.sa.gov.au/ Australian Museum https://australian.museum/ Museums Victoria https://museumsvictoria.com.au/ 2. Species Information 2.1. Details Specimen Contact: Museum Victoria - [email protected] Author: Walker, K. Citation: Walker, K. (2009) Native houstoni halictid bee(Homalictus (Homalictus) houstoni)Updated on 10/1/2011 Available online: PaDIL - http://www.padil.gov.au Image Use: Free for use under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY- NC 4.0) 2.2. URL Live link: http://www.padil.gov.au/pollinators/Pest/Main/138367 2.3. Facets Status: Native Australian Beneficial Species Host Genera: Fresh Flowers Bio-Region: Australasian - Oceanian Host Family: Santalaceae Female Frons sculpture: Reticulate Female Mesoscutum colour: Metallic Green Female Mesoscutum sculpture: Shiny - weakly punctate Female Propodeum: Posterior rim not carinate, Surface finely reticulate Male Clypeus colour: Without any yellow marking Male lower inner eye width: Narrower than upper inner width Male scape colour: Entirely black or brown 2.4. Diagnostic Notes Homalictus (Homalictus) houstoni Walker, 1986 Homalictus (Homalictus) houstoni Walker, K.L. 1986. Revision of the Australian species of the genus Homalictus Cockerell (Hymenoptera: Halictidae). Memoirs of Museum Victoria 47: 105–200 [141]. Type data:Holotype SAMA ?, 64 km E Norseman, WA. -
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. -
Stingless Bee Nesting Biology David W
Stingless bee nesting biology David W. Roubik To cite this version: David W. Roubik. Stingless bee nesting biology. Apidologie, Springer Verlag, 2006, 37 (2), pp.124-143. hal-00892207 HAL Id: hal-00892207 https://hal.archives-ouvertes.fr/hal-00892207 Submitted on 1 Jan 2006 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 37 (2006) 124–143 124 c INRA/DIB-AGIB/ EDP Sciences, 2006 DOI: 10.1051/apido:2006026 Review article Stingless bee nesting biology* David W. Ra,b a Smithsonian Tropical Research Institute, Apartado 0843-03092, Balboa, Ancón, Panamá, República de Panamá b Unit 0948, APO AA 34002-0948, USA Received 2 October 2005 – Revised 29 November 2005 – Accepted 23 December 2005 Abstract – Stingless bees diverged since the Cretaceous, have 50 times more species than Apis,andare both distinctive and diverse. Nesting is capitulated by 30 variables but most do not define clades. Both architectural features and behavior decrease vulnerability, and large genera vary in nest habit, architecture and defense. Natural stingless bee colony density is 15 to 1500 km−2. Symbionts include mycophagic mites, collembolans, leiodid beetles, mutualist coccids, molds, and ricinuleid arachnids. -
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.