HYGIENIC BEHAVIOR OF HONEY BEES IN RELATION TO CHALKBROOD DISEASE
Apidologie, 14 1 (1983) 29-39
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https://doi.org/10.1242/jeb.062562
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https://doi.org/10.1007/978-94-007-1942-2_18
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https://doi.org/10.1007/s10886-009-9683-8
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https://doi.org/10.1016/j.jinsphys.2008.07.016
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https://doi.org/10.1016/j.foreco.2007.04.005
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Jasna Kralj, Axel Brockmann, Stefan Fuchs and Jürgen TautzJournal of Comparative Physiology A 193 (3) 363 (2007)
https://doi.org/10.1007/s00359-006-0192-8
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https://doi.org/10.1051/apido:2006065
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https://doi.org/10.1016/j.anbehav.2006.01.018
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Martha GilliamFEMS Microbiology Letters 155 (1) 1 (2006)
https://doi.org/10.1111/j.1574-6968.1997.tb12678.x
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James D. Ellis, Keith S. Delaplane, Cameron S. Richards, et al.Annals of the Entomological Society of America 97 (4) 860 (2004)
https://doi.org/10.1603/0013-8746(2004)097[0860:HBOCAE]2.0.CO;2
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H.S. Arathi and M. SpivakAnimal Behaviour 62 (1) 57 (2001)
https://doi.org/10.1006/anbe.2000.1731
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Ciro InvernizziIheringia. Série Zoologia (91) 108 (2001)
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Advances in Microbial Ecology
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https://doi.org/10.1007/978-1-4757-9074-0_5
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Martha Gilliam, Stephen Taber, Brenda J. Lorenz and Dorothy B. PrestJournal of Invertebrate Pathology 52 (2) 314 (1988)
https://doi.org/10.1016/0022-2011(88)90141-3