Articles citing this article

The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).

Cited article:

Honey bee genetics shape the strain-level structure of gut microbiota in social transmission

Jiaqiang Wu, Haoyu Lang, Xiaohuan Mu, Zijing Zhang, Qinzhi Su, Xiaosong Hu and Hao Zheng
Microbiome 9 (1) (2021)
https://doi.org/10.1186/s40168-021-01174-y

Experimental increase of worker diversity benefits brood production in ants

Marina N. Psalti, Dustin Gohlke and Romain Libbrecht
BMC Ecology and Evolution 21 (1) (2021)
https://doi.org/10.1186/s12862-021-01890-x

Estimation of C-derived introgression into A. m. mellifera colonies in the Russian Urals using microsatellite genotyping

Rustem A. Ilyasov, Myeong-Lyeol Lee, Ural Yunusbaev, Alexey Nikolenko and Hyung-Wook Kwon
Genes & Genomics 42 (9) 987 (2020)
https://doi.org/10.1007/s13258-020-00966-0

Does multiple paternity influence offspring disease resistance?

K. E. Thonhauser, S. Raveh, M. Thoß and D. J. Penn
Journal of Evolutionary Biology 29 (6) 1142 (2016)
https://doi.org/10.1111/jeb.12854

The social mirror for division of labor: what network topology and dynamics can teach us about organization of work in insect societies

Danielle P. Mersch
Behavioral Ecology and Sociobiology 70 (7) 1087 (2016)
https://doi.org/10.1007/s00265-016-2104-4

Honey bee (Apis mellifera) intracolonial genetic diversity influences worker nutritional status

Bruce J. Eckholm, Ming H. Huang, Kirk E. Anderson, Brendon M. Mott and Gloria DeGrandi-Hoffman
Apidologie 46 (2) 150 (2015)
https://doi.org/10.1007/s13592-014-0311-4

Genetic diversity affects colony survivorship in commercial honey bee colonies

David R. Tarpy, Dennis vanEngelsdorp and Jeffrey S. Pettis
Naturwissenschaften 100 (8) 723 (2013)
https://doi.org/10.1007/s00114-013-1065-y

Multiple paternity in the freshwater snail, Potamopyrgus antipodarum

Deanna M. Soper, Lynda F. Delph and Curt M. Lively
Ecology and Evolution 2 (12) 3179 (2012)
https://doi.org/10.1002/ece3.408

Within- and across-colony effects of hyperpolyandry on immune function and body condition in honey bees (Apis mellifera)

Noah Wilson-Rich, David R. Tarpy and Philip T. Starks
Journal of Insect Physiology 58 (3) 402 (2012)
https://doi.org/10.1016/j.jinsphys.2011.12.020

Does Patriline Composition Change over a Honey Bee Queen’s Lifetime?

Robert Brodschneider, Gérard Arnold, Norbert Hrassnigg and Karl Crailsheim
Insects 3 (3) 857 (2012)
https://doi.org/10.3390/insects3030857

Recruitment-dance signals draw larger audiences when honey bee colonies have multiple patrilines

M. B. Girard, H. R. Mattila and T. D. Seeley
Insectes Sociaux 58 (1) 77 (2011)
https://doi.org/10.1007/s00040-010-0118-x

Effects of patriline on gustatory responsiveness and olfactory learning in honey bees

Ricarda Scheiner and Gérard Arnold
Apidologie 41 (1) 29 (2010)
https://doi.org/10.1051/apido/2009040

What is an Individual Organism? A Multilevel Selection Perspective

Henri J. Folse and Joan Roughgarden
The Quarterly Review of Biology 85 (4) 447 (2010)
https://doi.org/10.1086/656905

Task-dependent influence of genetic architecture and mating frequency on division of labour in social insect societies

Danesh Tarapore, Dario Floreano and Laurent Keller
Behavioral Ecology and Sociobiology 64 (4) 675 (2010)
https://doi.org/10.1007/s00265-009-0885-4

Intracolonial genetic variability in honeybee larval resistance to the chalkbrood and American foulbrood parasites

C. Invernizzi, F. Peñagaricano and I. H. Tomasco
Insectes Sociaux 56 (3) 233 (2009)
https://doi.org/10.1007/s00040-009-0016-2

Sustainable multiple queen colonies of honey bees, Apis mellifera ligustica

Huo-Qing Zheng, Shui-Hua Jin, Fu-Liang Hu and Christian W. W. Pirk
Journal of Apicultural Research 48 (4) 284 (2009)
https://doi.org/10.3896/IBRA.1.48.4.09

Division of labour and social insect colony performance in relation to task and mating number under two alternative response threshold models

R. Gove, M. Hayworth, M. Chhetri and O. Rueppell
Insectes Sociaux 56 (3) 319 (2009)
https://doi.org/10.1007/s00040-009-0028-y

Maintenance and application of multiple queen colonies in commercial beekeeping

Huo-Qing Zheng, Shui-Hua Jin, Fu-Liang Hu, Christian W W Pirk and Vincent Dietemann
Journal of Apicultural Research 48 (4) 290 (2009)
https://doi.org/10.3896/IBRA.1.48.4.10

Genetic diversity, worker size polymorphism and division of labour in the polyandrous ant Cataglyphis cursor

Denis Fournier, Geraldine Battaille, Iris Timmermans and Serge Aron
Animal Behaviour 75 (1) 151 (2008)
https://doi.org/10.1016/j.anbehav.2007.04.023

Split sex ratios in the social Hymenoptera: a meta-analysis

Joël Meunier, Stuart A. West and Michel Chapuisat
Behavioral Ecology 19 (2) 382 (2008)
https://doi.org/10.1093/beheco/arm143

Genetic diversity within honeybee colonies increases signal production by waggle-dancing foragers

Heather R Mattila, Kelly M Burke and Thomas D Seeley
Proceedings of the Royal Society B: Biological Sciences 275 (1636) 809 (2008)
https://doi.org/10.1098/rspb.2007.1620

Extra-pair paternity in alpine marmots, Marmota marmota: genetic quality and genetic diversity effects

A. Cohas, N. G. Yoccoz and D. Allainé
Behavioral Ecology and Sociobiology 61 (7) 1081 (2007)
https://doi.org/10.1007/s00265-006-0341-7

The principles of collective animal behaviour

D.J.T Sumpter
Philosophical Transactions of the Royal Society B: Biological Sciences 361 (1465) 5 (2006)
https://doi.org/10.1098/rstb.2005.1733

Experimental manipulation of colony genetic diversity had no effect on short-term task efficiency in the Argentine ant Linepithema humile

Herv� Rosset, Laurent Keller and Michel Chapuisat
Behavioral Ecology and Sociobiology 58 (1) 87 (2005)
https://doi.org/10.1007/s00265-004-0890-6

RELATIONSHIPS BETWEEN PHENOTYPE, MATING BEHAVIOR, AND FITNESS OF QUEENS IN THE ANT LASIUS NIGER

Else J. Fjerdingstad and Laurent Keller
Evolution 58 (5) 1056 (2004)
https://doi.org/10.1554/03-535

GENETIC DIVERSITY AND DISEASE RESISTANCE IN LEAF-CUTTING ANT SOCIETIES

William O. H. Hughes and Jacobus J. Boomsma
Evolution 58 (6) 1251 (2004)
https://doi.org/10.1554/03-546

Extreme queen‐mating frequency and colony fission in African army ants

DANIEL J. C. KRONAUER, CASPAR SCHÖNING, JES S. PEDERSEN, JACOBUS J. BOOMSMA and JÜRGEN GADAU
Molecular Ecology 13 (8) 2381 (2004)
https://doi.org/10.1111/j.1365-294X.2004.02262.x

THE EVOLUTION OF FEMALE MULTIPLE MATING IN SOCIAL HYMENOPTERA

Mark J. F. Brown and Paul Schmid-Hempel
Evolution 57 (9) 2067 (2003)
https://doi.org/10.1554/02-597

The relationship between multiple mating by queens, within-colony genetic variability and fitness in the ant Lasius niger

E. J. Fjerdingstad, P. J. Gertsch and L. Keller
Journal of Evolutionary Biology 16 (5) 844 (2003)
https://doi.org/10.1046/j.1420-9101.2003.00589.x

No Behavioral Control over Mating Frequency in Queen Honey Bees (Apis mellifera L.): Implications for the Evolution of Extreme Polyandry

David R. Tarpy and Robert E. Page, Jr.
The American Naturalist 155 (6) 820 (2000)
https://doi.org/10.1086/303358

Genetic effects on task performance, but not on age polyethism, in a swarm-founding eusocial wasp

SEAN O’DONNELL
Animal Behaviour 55 (2) 417 (1998)
https://doi.org/10.1006/anbe.1997.0627

Effects of worker genotypic diversity on honey bee colony development and behavior (Apis mellifera L.)

Robert E. Page, Gene E. Robinson, M. Kim Fondrk and Medhat E. Nasr
Behavioral Ecology and Sociobiology 36 (6) 387 (1995)
https://doi.org/10.1007/BF00177334