. Armanini, Genital tract infections and infertility, Eur. J. Obstet. Gynecol. Reprod. Biol, vol.140, pp.3-11, 2008.

E. Moretti, M. G. Federico, V. Giannerini, and G. , Sperm ultrastructure and meiotic segregation in a group of patients with chronic hepatitis B and C, Andrologia, vol.11, issue.3, pp.173-178, 2008.
DOI : 10.1016/S0168-8278(99)80239-6

N. C. Feki, N. Abid, A. Rebai, A. Sellami, B. B. Ayed et al., Semen Quality Decline Among Men in Infertile Relationships: Experience Over 12 Years in the South of Tunisia, Journal of Andrology, vol.30, issue.5, pp.541-547, 2009.
DOI : 10.2164/jandrol.108.005959

W. Mnif, A. I. Hassine, A. Bouaziz, A. Bartegi, O. Thomas et al., Effect of Endocrine Disruptor Pesticides: A Review, International Journal of Environmental Research and Public Health, vol.56, issue.12, pp.2265-2303, 2011.
DOI : 10.1016/j.yrtph.2009.09.013

URL : https://hal.archives-ouvertes.fr/hal-00878623

L. Multigner and A. Oliva, Environment as a Risk Factor for Male Infertility, The Scientific World JOURNAL, vol.1, pp.576-578, 2001.
DOI : 10.1100/tsw.2001.296

H. Levine and S. H. Swan, Is dietary pesticide exposure related to semen quality? Positive evidence from men attending a fertility clinic, Human Reproduction, vol.30, issue.6, pp.1287-1289, 2015.
DOI : 10.1093/humrep/dev065

URL : https://academic.oup.com/humrep/article-pdf/30/6/1287/1699678/dev065.pdf

C. R. Tyler, S. Jobling, and J. P. Sumpter, Endocrine Disruption in Wildlife: A Critical Review of the Evidence, Critical Reviews in Toxicology, vol.28, issue.4, pp.319-361, 1998.
DOI : 10.1080/10408449891344236

T. H. Hutchinson, Reproductive and developmental effects of endocrine disrupters in invertebrates: in vitro and in vivo approaches, Toxicology Letters, vol.131, issue.1-2, pp.75-81, 2002.
DOI : 10.1016/S0378-4274(02)00046-2

H. R. Kohler and R. Triebskorn, Wildlife Ecotoxicology of Pesticides: Can We Track Effects to the Population Level and Beyond?, Science, vol.1, issue.6081, pp.759-765, 2013.
DOI : 10.1126/science.1217909

L. S. Bauer and G. L. Nordin, Effect of Nosema fumiferanae (Microsporida) on Fecundity, Fertility, and Progeny Performance of Choristoneura fumiferana (Lepidoptera: Tortricidae), Environmental Entomology, vol.18, issue.2, pp.261-265, 1989.
DOI : 10.1093/ee/18.2.261

E. Delcacho, J. I. Marti, A. Josa, J. Quilez, and C. Sanchezacedo, Effect of Varroa jacobsoni parasitization in the glycoprotein expression on Apis mellifera spermatozoa, Apidologie, vol.27, issue.2, pp.87-92, 1996.
DOI : 10.1051/apido:19960203

P. Duay, Relation between the Level of Preimaginal Infestation by the Broodmite Varroa destructor and Adult Life Expectancy in Drone Honeybees (Hymenoptera: Apidae: Apis mellifera), Entomologia Generalis, vol.26, issue.3, pp.213-218, 2002.
DOI : 10.1127/entom.gen/26/2002/213

R. K. Seth, J. J. Kaur, D. K. Rao, and S. E. Reynolds, Effects of larval exposure to sublethal concentrations of the ecdysteroid agonists RH-5849 and tebufenozide (RH-5992) on male reproductive physiology in Spodoptera litura, Journal of Insect Physiology, vol.50, issue.6, pp.505-517, 2004.
DOI : 10.1016/j.jinsphys.2004.03.007

R. Miranda, Viruses associated with ovarian degeneration in Apis mellifera L. queens, PLoS One, vol.6, p.16217, 2011.

L. J. Brennan, J. A. Haukedal, J. C. Earle, B. Keddie, and H. L. Harris, Disruption of redox homeostasis leads to oxidative DNA damage in spermatocytes of Wolbachia-infected Drosophila simulans, Insect Molecular Biology, vol.265, issue.5, pp.510-520, 2012.
DOI : 10.1098/rspb.1998.0324

A. M. Collins and J. S. Pettis, Correlation of queen size and spermathecal contents and effects of miticide exposure during development, Apidologie, vol.19, issue.1, pp.351-356, 2013.
DOI : 10.1016/0022-1910(73)90225-4

URL : https://hal.archives-ouvertes.fr/hal-01201304

S. Misra, A. Singh, H. R. , V. Sharma, M. K. Reddy-mudiam et al., Identification of Drosophila-Based Endpoints for the Assessment and Understanding of Xenobiotic-Mediated Male Reproductive Adversities, Toxicological Sciences, vol.141, issue.1, pp.278-291, 2014.
DOI : 10.1093/toxsci/kfu125

Y. Peng, B. Baer-imhoof, A. H. Millar, and B. Baer, Consequences of Nosema apis infection for male honey bees and their fertility, Scientific Reports, vol.9, issue.1, p.10565, 2015.
DOI : 10.1002/pmic.200800708

L. Neumann and . Gauthier, Neonicotinoid pesticides severely affect honey bee queens, Sci. Rep, vol.5, p.14621, 2015.

G. Kairo, B. Provost, S. Tchamitchian, F. B. Abdelkader, M. Bonnet et al., Drone exposure to the systemic insecticide Fipronil indirectly impairs queen reproductive potential, Scientific Reports, vol.67, issue.90, p.31904, 2016.
DOI : 10.18637/jss.v067.i01

URL : https://hal.archives-ouvertes.fr/hal-01595366

V. Chaimanee, J. D. Evans, Y. P. Chen, C. Jackson, and J. S. Pettis, Sperm viability and gene expression in honey bee queens ( Apis mellifera ) following exposure to the neonicotinoid insecticide imidacloprid and the organophosphate acaricide coumaphos, Journal of Insect Physiology, vol.89, pp.1-8, 2016.
DOI : 10.1016/j.jinsphys.2016.03.004

M. L. Mccallum, M. Matlock, J. Treas, B. Safi, W. Sanson et al., Endocrine disruption of sexual selection by an estrogenic herbicide in the mealworm beetle (Tenebrio molitor), Ecotoxicology, vol.12, issue.4, pp.1461-1466, 2013.
DOI : 10.1093/beheco/12.6.761

A. L. Knight and L. Flexner, Disruption of mating in codling moth (Lepidoptera: Tortricidae) by chlorantranilipole, an anthranilic diamide insecticide, Pest Management Science, vol.36, issue.2, pp.180-189, 2007.
DOI : 10.1093/ee/25.6.1398

I. Laycock, K. M. Lenthall, A. T. Barratt, and J. E. , Effects of imidacloprid, a neonicotinoid pesticide, on reproduction in worker bumble bees (Bombus terrestris), Ecotoxicology, vol.40, issue.7, pp.1937-1945, 2012.
DOI : 10.1051/apido/2009025

K. T. Tassou and R. Schulz, Low field-relevant tebufenozide concentrations affect reproduction in Chironomus riparius (Diptera: Chironomidae) in a long-term toxicity test, Environmental Science and Pollution Research, vol.105, issue.436, pp.3735-3742, 2013.
DOI : 10.1126/science.241.4864.470

M. A. Costa, V. F. Moscardini, P. D. Gontijo, G. A. Carvalho, R. L. De-oliveira et al., Sublethal and transgenerational effects of insecticides in developing Trichogramma galloi (Hymenoptera: Trichogrammatidae), Ecotoxicology, vol.86, issue.8, pp.1399-1408, 2014.
DOI : 10.1007/s10340-013-0531-9

D. Xiao, T. Yang, N. Desneux, P. Han, and X. Gao, Assessment of Sublethal and Transgenerational Effects of Pirimicarb on the Wheat Aphids Rhopalosiphum padi and Sitobion avenae, PLOS ONE, vol.33, issue.6, p.128936, 2015.
DOI : 10.1371/journal.pone.0128936.t005

R. Pigeault, J. Vezilier, A. Nicot, S. Gandon, and A. Rivero, Transgenerational effect of infection in Plasmodium-infected mosquitoes, Biology Letters, vol.279, issue.1746, p.20141025, 2015.
DOI : 10.1098/rspb.2012.1841

B. Sures, Environmental parasitology: relevancy of parasites in monitoring environmental pollution, Trends in Parasitology, vol.20, issue.4, pp.170-177, 2004.
DOI : 10.1016/j.pt.2004.01.014

C. Vidau, H. Alaoui, D. G. Biron, and F. Delbac, Mais où sont passées les abeilles ?, Biofutur, vol.327, pp.56-59, 2011.

S. Kohler, A. Loureiro, A. L. Soares, C. Ferreira, A. Kienle et al., Interactions between effects of environmental chemicals and natural stressors: A review, Sci. Total Environ, vol.408, pp.3746-3762, 2010.

R. Relyea and J. Hoverman, Assessing the ecology in ecotoxicology: a review and synthesis in freshwater systems, Ecology Letters, vol.154, issue.suppl.1, pp.1157-1171, 2006.
DOI : 10.1127/archiv-hydrobiol/154/2002/413

A. Brillard, L. P. Baldy, Y. L. Belzunces, and . Conte, Interactions between Nosema microspores and a neonicotinoid weaken honeybees (Apis mellifera), Environ. Microbiol, vol.12, pp.774-782, 2010.

D. G. Texier, N. Biron, H. Blot, L. P. Alaoui, F. Belzunces et al., Exposure to sublethal doses of fipronil and thiacloprid highly increases mortality of honeybees previously infected by Nosema ceranae, PLoS One, vol.6, p.21550, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00814778

L. P. Vigues, F. Belzunces, N. Delbac, and . Blot, Parasite-insecticide interactions: a case study of Nosema ceranae and fipronil synergy on honeybee, Sci. Rep, vol.2, p.326, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00814027

G. Retschnig, P. Neumann, and G. R. Williams, Thiacloprid???Nosema ceranae interactions in honey bees: Host survivorship but not parasite reproduction is dependent on pesticide dose, Journal of Invertebrate Pathology, vol.118, pp.18-19, 2014.
DOI : 10.1016/j.jip.2014.02.008

J. Aufauvre, B. Misme-aucouturier, B. Vigues, C. Texier, F. Delbac et al., Transcriptome Analyses of the Honeybee Response to Nosema ceranae and Insecticides, PLoS ONE, vol.30, issue.3, p.91686, 2014.
DOI : 10.1371/journal.pone.0091686.s005

URL : https://hal.archives-ouvertes.fr/hal-01071042

F. Sanchez-bayo, D. Goulson, F. Pennacchio, F. Nazzi, K. Goka et al., Are bee diseases linked to pesticides? ??? A brief review, Environment International, vol.89, issue.90, pp.89-90, 2016.
DOI : 10.1016/j.envint.2016.01.009

URL : https://hal.archives-ouvertes.fr/hal-01326560

A. Cousin, J. L. Kretzschmar, Y. L. Brunet, and . Conte, Combined neonicotinoid pesticide and parasite stress alter honeybee queens' physiology and survival, Sci. Rep, vol.6, p.31430, 2016.

S. Kretzschmar, L. P. Maini, and . Belzunces, Chronic toxicity and physiological changes induced in the honey bee by the exposure to fipronil and Bacillus thuringiensis spores alone or combined, Ecotoxicol. Environ. Saf, vol.127, pp.205-213, 2016.

S. G. Potts, J. C. Biesmeijer, C. Kremen, P. Neumann, O. Schweiger et al., Global pollinator declines: trends, impacts and drivers, Trends in Ecology & Evolution, vol.25, issue.6, pp.345-353, 2010.
DOI : 10.1016/j.tree.2010.01.007

URL : http://www.intertropi.ufam.edu.br/docs/ecosystem_services.pdf

D. Goulson, E. Nicholls, C. Botias, and E. L. Rotheray, Bee declines driven by combined stress from parasites, pesticides, and lack of flowers, Science, vol.110, issue.1, p.1255957, 2015.
DOI : 10.1016/j.jip.2012.02.014

P. Neumann and N. Carreck, Honey bee colony losses, Journal of Apicultural Research, vol.49, issue.1, pp.1-6, 2010.
DOI : 10.3896/IBRA.1.49.1.20

URL : http://www.tandfonline.com/doi/pdf/10.3896/IBRA.1.49.1.01?needAccess=true

D. Vanengelsdorp and M. D. Meixner, A historical review of managed honey bee populations in Europe and the United States and the factors that may affect them, Journal of Invertebrate Pathology, vol.103, pp.80-95, 2010.
DOI : 10.1016/j.jip.2009.06.011

M. L. Winston, The Biology of the Honeybee, 1987.

B. Baer, bees, Apidologie, vol.36, issue.2, pp.187-200, 2005.
DOI : 10.1051/apido:2005013

URL : https://hal.archives-ouvertes.fr/hal-00892137

D. R. Tarpy, Genetic diversity within honeybee colonies prevents severe infections and promotes colony growth, Proceedings of the Royal Society B: Biological Sciences, vol.270, issue.1510, pp.99-103, 2003.
DOI : 10.1098/rspb.2002.2199

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1691209/pdf

H. R. Mattila and T. D. Seeley, Genetic Diversity in Honey Bee Colonies Enhances Productivity and Fitness, Science, vol.52, issue.1, pp.362-364, 2007.
DOI : 10.1146/annurev.ento.46.1.413

URL : http://www.bio-nica.info/biblioteca/mattila2007beegenetic.pdf

B. P. Oldroyd and J. H. , Large fitness benefits from polyandry in the honey bee, Apis mellifera, Trends in Ecology & Evolution, vol.23, issue.2, pp.59-60, 2008.
DOI : 10.1016/j.tree.2007.10.012

T. E. Rinderer, L. I. De-guzman, V. A. Lancaster, G. T. Delatte, and J. A. Stelzer, Varroa in the mating yard: I. The effects of Varroa jacobsoni and Apistan (R) on drone honey bees, Am. Bee J, vol.139, pp.134-139, 1999.

H. A. Sylvester, R. P. Watts, L. I. De-guzman, J. A. Stelzer, and T. E. Rinderer, Varroa in the mating yard: II. The effects of Varroa and fluvalinate on drone mating competitiveness, American Bee Journal, vol.139, pp.225-227, 1999.

A. M. Collins and J. S. Pettis, Effect of varroa infestation on semen quality, Am. Bee J, vol.141, pp.590-593, 2001.

L. Straub, L. Villamar-bouza, S. Bruckner, P. Chantawannakul, L. Gauthier et al., Neonicotinoid insecticides can serve as inadvertent insect contraceptives, Proceedings of the Royal Society B: Biological Sciences, vol.44, issue.4, p.20160506, 2016.
DOI : 10.1007/s13592-013-0199-4

URL : http://rspb.royalsocietypublishing.org/content/royprsb/283/1835/20160506.full.pdf

M. Higes, R. Martin-hernandez, and A. Meana, in Europe: an emergent type C nosemosis, Apidologie, vol.64, issue.3, pp.375-392, 2010.
DOI : 10.1080/0005772X.1983.11097918

A. Badiou-beneteau, A. Benneveau, F. Geret, H. Delatte, N. Becker et al., Honeybee biomarkers as promising tools to monitor environmental quality, Environment International, vol.60, pp.31-41, 2013.
DOI : 10.1016/j.envint.2013.07.002

URL : https://hal.archives-ouvertes.fr/hal-01456745

S. M. Carvalho, L. P. Belzunces, G. A. Carvalho, J. L. Brunet, and A. Badiou-beneteau, to insecticides, Environmental Toxicology and Chemistry, vol.139, issue.9, pp.2117-2124, 2013.
DOI : 10.1201/9780203218655.ch1

G. Bischoff, K. Kamp, and . Bienefeld, Secondary biomarkers of insecticide-induced stress of honey bee colonies and their relevance for overwintering strength, Ecotoxicol. Environ. Saf, vol.132, pp.379-389, 2016.

S. Kretzschmar, J. L. Suchail, C. Brunet, and . Alaux, Influence of pollen nutrition on honey bee health: do pollen quality and diversity matter?, PLoS One, vol.8, p.72016, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01327432

D. Vanengelsdorp, J. Hayes, R. M. Underwood, and J. Pettis, A Survey of Honey Bee Colony Losses in the U.S., Fall 2007 to Spring 2008, PLoS ONE, vol.32, issue.12, p.4071, 2008.
DOI : 10.1371/journal.pone.0004071.t006

R. Brodschneider, R. Moosbeckhofer, and K. Crailsheim, Surveys as a tool to record winter losses of honey bee colonies: a two year case study in Austria and South Tyrol, Journal of Apicultural Research, vol.119, issue.1
DOI : 10.3896/IBRA.1.49.1.03

W. Berg, W. Ritter, S. Muhlen, M. Gisder, G. Meixner et al., The German bee monitoring project: a long term study to understand periodically high winter losses of honey bee colonies, Apidologie, vol.41, pp.332-352, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00892101

B. A. Williams, Unique physiology of host-parasite interactions in microsporidia infections, Cellular Microbiology, vol.50, issue.1, pp.1551-1560, 2009.
DOI : 10.1128/9781555818227.ch5

Y. Moritz, C. Le-conte, and . Alaux, Gut pathology and responses to the microsporidium Nosema ceranae in the honey bee Apis mellifera, PLoS One, vol.7, p.37017, 2012.

Q. Huang, P. Kryger, Y. Le-conte, and R. F. Moritz, Survival and immune response of drones of a Nosemosis tolerant honey bee strain towards N. ceranae infections, Journal of Invertebrate Pathology, vol.109, issue.3, pp.297-302, 2012.
DOI : 10.1016/j.jip.2012.01.004

D. Nicodemo, M. A. Maioli, H. C. Medeiros, M. Guelfi, K. V. Balieira et al., Fipronil and imidacloprid reduce honeybee mitochondrial activity, Environmental Toxicology and Chemistry, vol.203, issue.9, pp.2070-2075, 2014.
DOI : 10.1007/BF00693012

. Malaspina, Effects of sublethal dose of fipronil on neuron metabolic activity of Africanized honeybees, Arch. Environ. Contam. Toxicol, vol.64, pp.456-466, 2013.

T. C. Roat, J. R. Santos-pinto, L. D. Santos, K. S. Santos, O. Malaspina et al., Modification of the brain proteome of Africanized honeybees (Apis mellifera) exposed to a sub???lethal doses of the insecticide fipronil, Ecotoxicology, vol.159, issue.6, pp.1659-1670, 2014.
DOI : 10.1016/j.agee.2012.06.020

X. Wang, M. A. Martinez, Q. Wu, I. Ares, M. R. Martinez-larranaga et al., Fipronil insecticide toxicology: oxidative stress and metabolism, Critical Reviews in Toxicology, vol.33, issue.10
DOI : 10.1021/jf505916f

D. Gibbons, C. Morrissey, and P. Mineau, A review of the direct and indirect effects of neonicotinoids and fipronil on vertebrate wildlife, Environmental Science and Pollution Research, vol.147, issue.16, pp.103-118, 2015.
DOI : 10.1007/s00442-005-0330-y

A. Morrissey, D. A. Noome, L. Pisa, J. Settele, J. D. Stark et al., Systemic insecticides (neonicotinoids and fipronil): trends, uses, mode of action and metabolites, Environ. Sci. Pollut. Res. Int, vol.22, pp.5-34, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01171969

A. Decourtye, J. Devillers, E. Genecque, K. Le-menach, H. Budzinski et al., Comparative Sublethal Toxicity of Nine Pesticides on Olfactory Learning Performances of the Honeybee Apis mellifera, Archives of Environmental Contamination and Toxicology, vol.9, issue.2, pp.242-250, 2005.
DOI : 10.1093/jee/77.1.70

A. K. Hassani, M. Dacher, M. Gauthier, and C. Armengaud, Effects of sublethal doses of fipronil on the behavior of the honeybee (Apis mellifera), Pharmacology Biochemistry and Behavior, vol.82, issue.1, pp.30-39, 2005.
DOI : 10.1016/j.pbb.2005.07.008

URL : https://hal.archives-ouvertes.fr/hal-00094532

Y. Aliouane, A. K. Hassani, V. Gary, C. Armengaud, M. Lambin et al., SUBCHRONIC EXPOSURE OF HONEYBEES TO SUBLETHAL DOSES OF PESTICIDES: EFFECTS ON BEHAVIOR, Environmental Toxicology and Chemistry, vol.28, issue.1, pp.113-122, 2009.
DOI : 10.1897/08-110.1

URL : https://hal.archives-ouvertes.fr/hal-00318756

A. Bernadou, F. Demares, T. Couret-fauvel, J. C. Sandoz, and M. Gauthier, Effect of fipronil on side-specific antennal tactile learning in the honeybee, Journal of Insect Physiology, vol.55, issue.12, pp.1099-1106, 2009.
DOI : 10.1016/j.jinsphys.2009.08.019

A. Decourtye, S. Lefort, J. Devillers, M. Gauthier, P. Aupinel et al., Sublethal effects of fipronil on the ability of honeybees (Apis mellifera L.) to orientate in a complex maze. Julius-Kühn-Archiv, pp.75-83, 2010.

S. Camazine, I. Cakmak, K. Cramp, J. Finley, J. Fisher et al., How healthy are commercially-produced US honey bee queens? Am, Bee J, vol.138, pp.677-680, 1998.

J. Rhodes and D. Somerville, Introduction and Early Performance of Queen Bees: Some Factors Affecting Success : a Report for the Rural Industries Research and Development Corporation (Rural Industries Research and Development Corporation, 2003.

F. B. Abdelkader, G. Kairo, S. Tchamitchian, M. Cousin, J. Senechal et al., Semen quality of honey bee drones maintained from emergence to sexual maturity under laboratory, semi-field and field conditions, Apidologie, vol.8, issue.2, pp.215-223, 2014.
DOI : 10.1080/00218839.1969.11100220

URL : https://hal.archives-ouvertes.fr/hal-01234717

A. Meana, R. Martín-hernández, and M. Higes, infections in honey bees, Journal of Apicultural Research, vol.5, issue.2, pp.212-214, 2010.
DOI : 10.1111/j.1758-2229.2009.00018.x

M. Krupke, E. Liess, M. Long, E. A. Marzaro, D. A. Mitchell et al., Environmental fate and exposure; neonicotinoids and fipronil, Environ. Sci. Pollut. Res. Int, vol.22, pp.35-67, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01170672

S. W. Cobey, Comparison studies of instrumentally inseminated and naturally mated honey bee queens and factors affecting their performance, Apidologie, vol.1, issue.4, pp.390-410, 2007.
DOI : 10.1080/00218839.1995.11100895

URL : https://hal.archives-ouvertes.fr/hal-00892280

L. P. Belzunces, J. Lenoir-rousseaux, and M. Bounias, Properties of acetylcholinesterase from Apis mellifera heads, Insect Biochemistry, vol.18, issue.8, pp.811-819, 1988.
DOI : 10.1016/0020-1790(88)90105-9

G. L. Ellman, K. D. Courtney, V. Andres, and R. M. Featherstone, A new and rapid colorimetric determination of acetylcholinesterase activity, Biochemical Pharmacology, vol.7, issue.2, pp.88-95, 1961.
DOI : 10.1016/0006-2952(61)90145-9

M. Bounias, I. Kruk, M. Nectoux, and D. Popeskovic, Toxicology of Cupric Salts on Honeybees. V. Gluconate and Sulfate Action on Gut Alkaline and Acid Phosphatases, Ecotoxicology and Environmental Safety, vol.35, issue.1, pp.67-76, 1996.
DOI : 10.1006/eesa.1996.0082

G. Gomori, Human esterases, J. Lab. Clin. Med, vol.42, pp.445-453, 1953.

I. A. Cree and P. E. Andreotti, Measurement of cytotoxicity by ATP-based luminescence assay in primary cell cultures and cell lines, Toxicology in Vitro, vol.11, issue.5, pp.553-556, 1997.
DOI : 10.1016/S0887-2333(97)00060-X

H. Al-lawati, G. Kamp, and K. Bienefeld, Characteristics of the spermathecal contents of old and young honeybee queens, Journal of Insect Physiology, vol.55, issue.2, pp.116-121, 2009.
DOI : 10.1016/j.jinsphys.2008.10.010

W. H. Habig, M. J. Pabst, W. B. Jakoby, and S. Glutathione, The first enzymatic step in mercapturic acid formation, J. Biol. Chem, vol.249, pp.7130-7139, 1974.

R. F. Beers, J. , and I. W. Sizer, A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase, J. Biol. Chem, vol.195, pp.133-140, 1952.

D. Bates, M. Maechler, B. Bolker, and S. Walker, Fitting linear mixed-effects models using lme4, J. Stat. Softw, vol.67, pp.1-48, 2015.

S. Dray and A. Dufour, The ade4 package: Implementing the duality diagram for ecologists, J. Stat. Softw, vol.22, pp.1-20, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00434575

G. Caraux and S. Pinloche, PermutMatrix: a graphical environment to arrange gene expression profiles in optimal linear order, Bioinformatics, vol.21, issue.7, pp.1280-1281, 2005.
DOI : 10.1093/bioinformatics/bti141

URL : https://hal.archives-ouvertes.fr/lirmm-00105307

N. Gallai, J. Salles, J. Settele, and B. Vaissiere, Economic valuation of the vulnerability of world agriculture confronted with pollinator decline, Ecological Economics, vol.68, issue.3, pp.810-821, 2009.
DOI : 10.1016/j.ecolecon.2008.06.014

URL : https://hal.archives-ouvertes.fr/halshs-01293686

S. Potts, J. Biesmeijer, C. Kremen, P. Neumann, O. Schweiger et al., Global pollinator declines: trends, impacts and drivers, Trends in Ecology & Evolution, vol.25, issue.6, pp.345-353, 2010.
DOI : 10.1016/j.tree.2010.01.007

URL : http://www.intertropi.ufam.edu.br/docs/ecosystem_services.pdf

L. Burley, R. Fell, and R. Saacke, Survival of Honey Bee (Hymenoptera: Apidae) Spermatozoa Incubated at Room Temperature from Drones Exposed to Miticides, Journal of Economic Entomology, vol.101, issue.4, pp.1081-1087, 2008.
DOI : 10.1093/jee/101.4.1081

A. Collins and J. Pettis, Correlation of queen size and spermathecal contents and effects of miticide exposure during development, Apidologie, vol.19, issue.1, pp.351-356, 2013.
DOI : 10.1016/0022-1910(73)90225-4

URL : https://hal.archives-ouvertes.fr/hal-01201304

V. Chaimanee, J. Evans, Y. Chen, C. Jackson, and J. Pettis, Sperm viability and gene expression in honey bee queens ( Apis mellifera ) following exposure to the neonicotinoid insecticide imidacloprid and the organophosphate acaricide coumaphos, Journal of Insect Physiology, vol.89, pp.1-8, 2016.
DOI : 10.1016/j.jinsphys.2016.03.004

G. Williams, A. Troxler, G. Retschnig, K. Roth, O. Yañez et al., Neonicotinoid pesticides severely affect honey bee queens, Scientific Reports, vol.23, p.14621, 2015.
DOI : 10.3896/IBRA.1.52.4.13

URL : http://www.nature.com/articles/srep14621.pdf

G. Kairo, B. Provost, S. Tchamitchian, B. Abdelkader, F. Bonnet et al., Drone exposure to the systemic insecticide Fipronil indirectly impairs queen reproductive potential, Scientific Reports, vol.67, issue.90, 2016.
DOI : 10.18637/jss.v067.i01

URL : https://hal.archives-ouvertes.fr/hal-01595366

B. Abdelkader, F. Kairo, G. Tchamitchian, S. Cousin, M. Senechal et al., Semen quality of honey bee drones maintained from emergence to sexual maturity under laboratory, semi-field and field conditions, Apidologie, vol.8, issue.2, pp.215-223, 2014.
DOI : 10.1080/00218839.1969.11100220

URL : https://hal.archives-ouvertes.fr/hal-01234717

D. Bates, M. Maechler, B. Bolker, and S. Walker, Fitting Linear Mixed-Effects Models Using lme4, J Stat Softw, vol.67, pp.1-48, 2015.

N. Desneux, A. Decourtye, and J. Delpuech, The Sublethal Effects of Pesticides on Beneficial Arthropods, Annual Review of Entomology, vol.52, issue.1, pp.81-106, 2007.
DOI : 10.1146/annurev.ento.52.110405.091440

URL : https://hal.archives-ouvertes.fr/hal-00434587

L. Pisa, V. Amaral-rogers, L. Belzunces, J. Bonmatin, C. Downs et al., Effects of neonicotinoids and fipronil on non-target invertebrates, Environmental Science and Pollution Research, vol.30, issue.425, pp.68-102, 2015.
DOI : 10.1016/j.cropro.2010.10.006

URL : https://hal.archives-ouvertes.fr/hal-01171771

D. Vanengelsdorp and M. Meixner, A historical review of managed honey bee populations in Europe and the United States and the factors that may affect them, Journal of Invertebrate Pathology, vol.103, pp.80-95, 2010.
DOI : 10.1016/j.jip.2009.06.011

J. Free and I. Williams, Factors determining the rearing and rejection of drones by the honeybee colony, Animal Behaviour, vol.23, pp.650-675, 1975.
DOI : 10.1016/0003-3472(75)90143-8

K. Boes, Honeybee colony drone production and maintenance in accordance with environmental factors: an interplay of queen and worker decisions, Insectes Sociaux, vol.57, issue.1, pp.1-9, 2010.
DOI : 10.1007/s00040-009-0046-9

M. Sturup, B. Baer-imhoof, D. Nash, J. Boomsma, and B. Baer, When every sperm counts: factors affecting male fertility in the honeybee Apis mellifera, Behavioral Ecology, vol.24, issue.5, pp.1192-1198, 2013.
DOI : 10.1093/beheco/art049

M. Bienkowska, B. Panasiuk, P. Wegrzynowicz, and D. Gerula, The effect of different thermal conditions on drone semen quality and number of spermatozoa entering the spermatheca of queen bee, J Apic Sci, vol.55, pp.161-168, 2011.

A. Rousseau and P. Giovenazzo, Optimizing Drone Fertility With Spring Nutritional Supplements to Honey Bee (Hymenoptera: Apidae) Colonies, Journal of Economic Entomology, vol.109, issue.3, pp.1009-1014, 2016.
DOI : 10.1093/jee/tow056

M. Blum, Z. Glowska, and S. Taber, Chemistry of the Drone Honey Bee Reproductive System. II. Carbohydrates in the Reproductive Organs and Semen, Annals of the Entomological Society of America, vol.55, issue.1, pp.135-139, 1962.
DOI : 10.1093/aesa/55.1.135

L. Verma and R. Shuel, Respiratory metabolism of the semen of the honey-bee, Apis mellifera, Journal of Insect Physiology, vol.19, issue.1, pp.97-103, 1973.
DOI : 10.1016/0022-1910(73)90225-4

B. Baer, J. Heazlewood, N. Taylor, H. Eubel, and A. Millar, The seminal fluid proteome of the honeybee Apis mellifera, PROTEOMICS, vol.38, issue.8, pp.2085-2097, 2009.
DOI : 10.1002/pmic.200800708

R. Schmuck, T. Stadler, and H. Schmidt, Field relevance of a synergistic effect observed in the laboratory between an EBI fungicide and a chloronicotinyl insecticide in the honeybee (Apis mellifera L, Hymenoptera), Pest Management Science, vol.5, issue.3, pp.279-286, 2003.
DOI : 10.1111/j.1365-2338.1992.tb00483.x

E. Pilling, P. Campbell, M. Coulson, N. Ruddle, and I. Tornier, A Four-Year Field Program Investigating Long-Term Effects of Repeated Exposure of Honey Bee Colonies to Flowering Crops Treated with Thiamethoxam, PLoS ONE, vol.68, issue.3, 2013.
DOI : 10.1371/journal.pone.0077193.s025

N. Carreck and F. Ratnieksi, The dose makes the poison: have ???field realistic??? rates of exposure of bees to neonicotinoid insecticides been overestimated in laboratory studies?, Journal of Apicultural Research, vol.56, issue.1, pp.607-614, 2014.
DOI : 10.1126/science.1215025

H. Thompson, M. Coulson, N. Ruddle, S. Wilkins, and S. Harkin, Thiamethoxam: Assessing flight activity of honeybees foraging on treated oilseed rape using radio frequency identification technology, Environmental Toxicology and Chemistry, vol.44, issue.2, pp.385-393, 2016.
DOI : 10.1016/j.exger.2009.04.003

J. Van-der-sluijs, V. Amaral-rogers, L. Belzunces, M. Van-lexmond, J. Bonmatin et al., Conclusions of the Worldwide Integrated Assessment on the risks of neonicotinoids and fipronil to biodiversity and ecosystem functioning, Conclusions of the Worldwide Integrated Assessment on the risks of neonicotinoids and fipronil to biodiversity and ecosystem functioning, pp.148-154, 2015.
DOI : 10.1126/science.1215025

URL : https://hal.archives-ouvertes.fr/hal-01171970

A. Agarwal, R. A. Saleh, and M. A. Bedaiwy, Role of reactive oxygen species in the pathophysiology of human reproduction, Fertility and Sterility, vol.79, issue.4, pp.829-843, 2003.
DOI : 10.1016/S0015-0282(02)04948-8

H. Al-lawati, G. Kamp, and K. Bienefeld, Characteristics of the spermathecal contents of old and young honeybee queens, Journal of Insect Physiology, vol.55, issue.2, pp.116-121, 2009.
DOI : 10.1016/j.jinsphys.2008.10.010

C. Alaux, J. L. Brunet, C. Dussaubat, F. Mondet, S. Tchamitchan et al., ), Environmental Microbiology, vol.102, issue.3, pp.774-782, 2010.
DOI : 10.1093/jee/92.5.1125

C. Alaux, M. Folschweiller, C. Mcdonnell, D. Beslay, M. Cousin et al., Pathological effects of the microsporidium Nosema ceranae on honey bee queen physiology (Apis mellifera), Journal of Invertebrate Pathology, vol.106, issue.3, pp.380-385, 2011.
DOI : 10.1016/j.jip.2010.12.005

E. Alumot, Y. Lensky, and P. Holstein, Sugars and trehalase in the reproductive organs and hemolymph of the queen and drone honey bees (Apis mellifica L. var. Ligustica spin.), Comparative Biochemistry and Physiology, vol.28, issue.3, pp.1419-1425, 1969.
DOI : 10.1016/0010-406X(69)90579-9

J. Aufauvre, D. G. Biron, C. Vidau, R. Fontbonne, M. Roudel et al., Parasite-insecticide interactions: a case study of Nosema ceranae and fipronil synergy on honeybee, Scientific Reports, vol.30, issue.1, 2012.
DOI : 10.1051/apido:19990503

URL : https://hal.archives-ouvertes.fr/hal-00814027

J. Auger, J. M. Kunstmann, F. Czyglik, and P. Jouannet, Decline in Semen Quality among Fertile Men in Paris during the Past 20 Years, New England Journal of Medicine, vol.332, issue.5, pp.281-285, 1995.
DOI : 10.1056/NEJM199502023320501

A. Badiou-beneteau, A. Benneveau, F. Geret, H. Delatte, N. Becker et al., Honeybee biomarkers as promising tools to monitor environmental quality, Environment International, vol.60, pp.31-41, 2013.
DOI : 10.1016/j.envint.2013.07.002

URL : https://hal.archives-ouvertes.fr/hal-01456745

B. Baer, J. Collins, K. Maalaps, and S. P. Den-boer, ) queens, Ecology and Evolution, vol.45, issue.9, 2016.
DOI : 10.1016/S0022-1910(99)00056-6

B. Baer, J. L. Heazlewood, N. L. Taylor, H. Eubel, and A. H. Millar, The seminal fluid proteome of the honeybee Apis mellifera, PROTEOMICS, vol.38, issue.8, pp.2085-2097, 2009.
DOI : 10.1002/pmic.200800708

B. Baer and P. Schmid-hempel, Experimental variation in polyandry affects parasite loads and fitness in a bumble-bee, Nature, vol.355, issue.6715, pp.151-154, 1999.
DOI : 10.1038/355440a0

Z. Barganska, M. Slebioda, and J. Namiesnik, Honey bees and their products: Bioindicators of environmental contamination, Critical Reviews in Environmental Science and Technology, vol.147, issue.3, 2016.
DOI : 10.3896/IBRA.1.49.1.12

E. Baudry, M. Solignac, L. Garnery, M. Gries, J. Cornuet et al., Relatedness among honeybees (Apis mellifera) of a drone congregation, Proc. Roy. Soc, 1998.
DOI : 10.1098/rspb.1998.0533

L. S. Bauer and G. L. Nordin, Effect of Nosema fumiferanae (Microsporida) on Fecundity, Fertility, and Progeny Performance of Choristoneura fumiferana (Lepidoptera: Tortricidae), Environmental Entomology, vol.18, issue.2, pp.261-265, 1989.
DOI : 10.1093/ee/18.2.261

J. C. Biesmeijer, S. P. Roberts, M. Reemer, R. Ohlemuller, M. Edwards et al., Parallel Declines in Pollinators and Insect-Pollinated Plants in Britain and the Netherlands, Science, vol.313, issue.5785, pp.351-354, 2006.
DOI : 10.1126/science.1127863

M. S. Blum and S. Taber, Chemistry of the drone honey bee reproductive system???III. Dehydrogenases in washed spermatozoa, Journal of Insect Physiology, vol.11, issue.11, 1965.
DOI : 10.1016/0022-1910(65)90165-4

K. E. Boes, Honeybee colony drone production and maintenance in accordance with environmental factors: an interplay of queen and worker decisions, Insectes Sociaux, vol.57, issue.1, pp.40-49, 2010.
DOI : 10.1007/s00040-009-0046-9

S. Bogdanov, Contaminants of bee products, Apidologie, vol.56, issue.1, pp.1-18, 2006.
DOI : 10.1080/0005772X.2002.11099544

URL : https://hal.archives-ouvertes.fr/hal-00892166

J. M. Bonmatin, C. Giorio, V. Girolami, D. Goulson, D. P. Kreutzweiser et al., Environmental fate and exposure; neonicotinoids and fipronil, Environmental Science and Pollution Research, vol.55, issue.5, 2015.
DOI : 10.1002/(SICI)1096-9063(199904)55:4<482::AID-PS932>3.0.CO;2-3

URL : https://hal.archives-ouvertes.fr/hal-01170672

R. Brodschneider, R. Moosbeckhofer, and K. Crailsheim, Surveys as a tool to record winter losses of honey bee colonies: a two year case study in Austria and South Tyrol, Journal of Apicultural Research, vol.119, issue.1, pp.23-30, 2010.
DOI : 10.3896/IBRA.1.49.1.03

L. M. Burley, R. D. Fell, and R. G. Saacke, Survival of Honey Bee (Hymenoptera: Apidae) Spermatozoa Incubated at Room Temperature from Drones Exposed to Miticides, Journal of Economic Entomology, vol.101, issue.4, pp.1081-1087, 2008.
DOI : 10.1093/jee/101.4.1081

S. Camazine, I. Cakmak, K. Cramp, J. Finley, J. Fisher et al., How healthy are commercially-produced US honey bee queens? Am, Bee J, vol.138, issue.9, pp.677-680, 1998.

E. Carlsen, A. Giwercman, N. Keiding, and N. E. Skakkebaek, Evidence for decreasing quality of semen during past 50 years., BMJ, vol.305, issue.6854, pp.609-613, 1992.
DOI : 10.1136/bmj.305.6854.609

R. Carson, Silent spring, 1962.

S. M. Carvalho, L. P. Belzunces, G. A. Carvalho, J. L. Brunet, and A. Badiou-beneteau, to insecticides, Environmental Toxicology and Chemistry, vol.139, issue.9, pp.2117-2124, 2013.
DOI : 10.1201/9780203218655.ch1

V. Chaimanee, J. D. Evans, Y. P. Chen, C. Jackson, and J. S. Pettis, Sperm viability and gene expression in honey bee queens ( Apis mellifera ) following exposure to the neonicotinoid insecticide imidacloprid and the organophosphate acaricide coumaphos, Journal of Insect Physiology, vol.89, 2016.
DOI : 10.1016/j.jinsphys.2016.03.004

G. T. Chandler, T. L. Cary, D. C. Volz, S. S. Walse, J. L. Ferry et al., FIPRONIL EFFECTS ON ESTUARINE COPEPOD (AMPHIASCUS TENUIREMIS) DEVELOPMENT, FERTILITY, AND REPRODUCTION: A RAPID LIFE-CYCLE ASSAY IN 96-WELL MICROPLATE FORMAT, Environmental Toxicology and Chemistry, vol.23, issue.1, pp.117-124, 1897.
DOI : 10.1897/03-124

A. Ciereszko, J. Wilde, G. J. Dietrich, M. Siuda, B. B?k et al., Sperm parameters of honeybee drones exposed to imidacloprid, Apidologie, vol.5, issue.6079, pp.1-12, 2016.
DOI : 10.1038/srep14621

URL : https://hal.archives-ouvertes.fr/hal-01591722

S. W. Cobey, Comparison studies of instrumentally inseminated and naturally mated honey bee queens and factors affecting their performance, Apidologie, vol.1, issue.4, pp.390-410, 1051.
DOI : 10.1080/00218839.1995.11100895

URL : https://hal.archives-ouvertes.fr/hal-00892280

S. W. Cobey, D. R. Tarpy, and J. Woyke, queens, Journal of Apicultural Research, vol.124, issue.4, 2013.
DOI : 10.1051/apido:19920305

URL : https://hal.archives-ouvertes.fr/hal-00892280

L. M. Cole, R. A. Nicholson, and J. E. Casida, Action of Phenylpyrazole Insecticides at the GABA-Gated Chloride Channel, Pesticide Biochemistry and Physiology, vol.46, issue.1, pp.47-54, 1993.
DOI : 10.1006/pest.1993.1035

M. E. Colin and L. P. Belzunces, L.: a convenient biological approach, Pesticide Science, vol.27, issue.2, pp.115-119, 1992.
DOI : 10.1002/ps.2780270406

URL : https://hal.archives-ouvertes.fr/hal-01038037

A. M. Collins, Relationship between semen quality and performance of instrumentally inseminated honey bee queens, Apidologie, vol.31, issue.3, pp.421-429, 1051.
DOI : 10.1051/apido:2000132

URL : https://hal.archives-ouvertes.fr/hal-00891723

A. M. Collins and A. M. Donoghue, Viability assessment of honey bee, Apis mellifera, sperm using dual fluorescent staining, Theriogenology, vol.51, issue.8, pp.1513-1523, 1999.
DOI : 10.1016/S0093-691X(99)00094-1

A. M. Collins and J. S. Pettis, Effect of varroa infestation on semen quality, Am, 2001.

A. M. Collins and J. S. Pettis, Correlation of queen size and spermathecal contents and effects of miticide exposure during development, Apidologie, vol.19, issue.1, pp.351-356, 2013.
DOI : 10.1016/0022-1910(73)90225-4

URL : https://hal.archives-ouvertes.fr/hal-01201304

M. A. Costa, V. F. Moscardini, P. D. Gontijo, G. A. Carvalho, R. L. De-oliveira et al., Sublethal and transgenerational effects of insecticides in developing Trichogramma galloi (Hymenoptera: Trichogrammatidae), Ecotoxicology, vol.86, issue.8, pp.1399-1408, 2014.
DOI : 10.1007/s10340-013-0531-9

D. Cruz-landim and C. , Aparelho reprodutor e gametogênese ABELHAS : Morfologia e funçào de sistemas, 2009.

H. A. Dade, Anatomy and Dissection of the Honeybee, 1994.

E. Delcacho, J. I. Marti, A. Josa, J. Quilez, and C. Sanchezacedo, Effect of Varroa jacobsoni parasitization in the glycoprotein expression on Apis mellifera spermatozoa, Apidologie, vol.27, issue.2, pp.87-92, 1996.
DOI : 10.1051/apido:19960203

N. Desneux, A. Decourtye, and J. M. Delpuech, The Sublethal Effects of Pesticides on Beneficial Arthropods, Annual Review of Entomology, vol.52, issue.1, pp.81-106, 2007.
DOI : 10.1146/annurev.ento.52.110405.091440

URL : https://hal.archives-ouvertes.fr/hal-00434587

D. Pasquale, G. Salignon, M. , L. Conte, Y. Belzunces et al., Influence of Pollen Nutrition on Honey Bee Health: Do Pollen Quality and Diversity Matter?, PLoS ONE, vol.27, issue.8, 2013.
DOI : 10.1371/journal.pone.0072016.s003

P. Duay, Relation between the Level of Preimaginal Infestation by the Broodmite Varroa destructor and Adult Life Expectancy in Drone Honeybees (Hymenoptera: Apidae: Apis mellifera), Entomologia Generalis, vol.26, issue.3, pp.213-218, 2002.
DOI : 10.1127/entom.gen/26/2002/213

C. Dussaubat, J. L. Brunet, M. Higes, J. K. Colbourne, J. Lopez et al., Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera, PLoS ONE, vol.35, issue.5, 2012.
DOI : 10.1371/journal.pone.0037017.s006

C. Dussaubat, A. Maisonnasse, D. Crauser, S. Tchamitchian, M. Bonnet et al., Combined neonicotinoid pesticide and parasite stress alter honeybee queens??? physiology and survival, Scientific Reports, vol.195, issue.90, p.10, 1038.
DOI : 10.3896/IBRA.1.52.1.14

URL : http://www.nature.com/articles/srep31430.pdf

. Franceagrimer, Audit économique de la filière apicole française, pp.1-32, 2012.

L. Gauthier, M. Ravallec, M. Tournaire, F. Cousserans, M. Bergoin et al., Viruses Associated with Ovarian Degeneration in Apis mellifera L. Queens, PLoS ONE, vol.37, issue.1, 2011.
DOI : 10.1371/journal.pone.0016217.s004

H. V. Gencer and Y. Kahya, L.) queens, Journal of Apicultural Research, vol.50, issue.3, pp.190-194, 2011.
DOI : 10.1051/apido:19780304

B. Gessner and K. Gessner, Inorganic ions in spermathecal fluid and their transport across the spermathecal membrane of the queen bee, Apis mellifera, Journal of Insect Physiology, vol.22, issue.11, pp.1469-1474, 1976.
DOI : 10.1016/0022-1910(76)90212-2

B. Gessner and F. Ruttner, Transfer of spermatozoa into spermatheca of honey bee queen, Apidologie, vol.8, issue.1, 1977.

D. Gibbons, C. Morrissey, and P. Mineau, A review of the direct and indirect effects of neonicotinoids and fipronil on vertebrate wildlife, Environmental Science and Pollution Research, vol.147, issue.16, pp.103-118, 2015.
DOI : 10.1007/s00442-005-0330-y

D. Goulson, E. Nicholls, C. Botias, and E. L. Rotheray, Bee declines driven by combined stress from parasites, pesticides, and lack of flowers, Science, vol.110, issue.1, 2015.
DOI : 10.1016/j.jip.2012.02.014

L. J. Guillette, . Jr, and E. A. Guillette, Environmental Contaminants and Reproductive Abnormalities in Wildlife: Implications for Public Health?, Toxicology and Industrial Health, vol.135, issue.2, pp.3-4, 1996.
DOI : 10.1210/endo.135.1.8013351

M. Haberl and D. Tautz, Sperm usage in honey bees, Behavioral Ecology and Sociobiology, vol.42, issue.4, pp.247-255, 1998.
DOI : 10.1007/s002650050436

R. Habert, G. Livera, and V. Rouiller-fabre, Toxicologie de la reproduction. La reproduction animale et humaine. M. Saint-Dizier and S. Chastant-Maillard, pp.507-531, 2014.

J. R. Harbo, The Rate of Depletion of Spermatozoa in the Queen Honeybee Spermatheca, Journal of Apicultural Research, vol.5, issue.2, pp.204-207, 1979.
DOI : 10.1080/00218839.1979.11099969

M. Higes, R. Martin-hernandez, and A. Meana, in Europe: an emergent type C nosemosis, Apidologie, vol.64, issue.3, pp.375-392, 2010.
DOI : 10.1080/0005772X.1983.11097918

T. C. Hornshaw, R. J. Aulerich, and H. E. Johnson, Feeding great lakes fish to mink: Effects on mink and accumulation and elimination of PCBS by mink, Journal of Toxicology and Environmental Health, vol.6, issue.9, pp.933-946, 1983.
DOI : 10.1007/BF01540092

D. J. Hosken, P. Stockley, and M. T. Clegg, Benefits of Polyandry: A Life History Perspective, Evol. Biol. R. J. Macintyre, pp.173-194, 2003.
DOI : 10.1007/978-1-4757-5190-1_4

O. Kaftanoglu and Y. Peng, Preservation of Honeybee Spermatozoa in Liquid Nitrogen, Journal of Apicultural Research, vol.113, issue.11, pp.157-163, 1984.
DOI : 10.1051/apido:19780301

S. Khan, M. H. Jan, D. Kumar, and A. G. Telang, Firpronil induced spermotoxicity is associated with oxidative stress, DNA damage and apoptosis in male rats, Pesticide Biochemistry and Physiology, vol.124, pp.8-14, 2015.
DOI : 10.1016/j.pestbp.2015.03.010

M. King, H. Eubel, A. H. Millar, and B. Baer, Proteins within the seminal fluid are crucial to keep sperm viable in the honeybee Apis mellifera, Journal of Insect Physiology, vol.57, issue.3, pp.409-414, 2011.
DOI : 10.1016/j.jinsphys.2010.12.011

M. Kitulagodage, W. A. Buttemer, and L. B. Astheimer, Adverse effects of fipronil on avian reproduction and development: maternal transfer of fipronil to eggs in zebra finch Taeniopygia guttata and in ovo exposure in chickens Gallus domesticus, Ecotoxicology, vol.227, issue.5259, pp.653-660, 2011.
DOI : 10.1038/227737a0

A. L. Knight and L. Flexner, Disruption of mating in codling moth (Lepidoptera: Tortricidae) by chlorantranilipole, an anthranilic diamide insecticide, Pest Management Science, vol.36, issue.2, pp.180-189, 1318.
DOI : 10.1093/ee/25.6.1398

G. Koeniger, Reproduction and Mating Behavior, Bee Genetics and Breeding. T, 1986.
DOI : 10.1016/B978-0-12-588920-9.50015-7

H. H. Laidlaw and R. E. Page, Polyandry in honey bees (Apis-mellifera L) - Sperm Utilization And Intracolony Genetic-Relationships, Genetics, vol.108, issue.4, pp.985-997, 1984.

M. M. Laronda, K. Unno, L. M. Butler, and T. Kurita, The development of cervical and vaginal adenosis as a result of diethylstilbestrol exposure in utero, Differentiation, vol.84, issue.3, pp.252-260, 2012.
DOI : 10.1016/j.diff.2012.05.004

I. Laycock, K. M. Lenthall, A. T. Barratt, and J. E. Cresswell, Effects of imidacloprid, a neonicotinoid pesticide, on reproduction in worker bumble bees (Bombus terrestris), Ecotoxicology, vol.40, issue.7, pp.1937-1945, 2012.
DOI : 10.1051/apido/2009025

Y. Lensky, E. Ben-david, and H. Schindler, Ultrastructure of the Spermatozoon of the Mature Drone Honeybee, Journal of Apicultural Research, vol.2, issue.4, pp.264-271, 1979.
DOI : 10.1139/g65-081

Y. Lensky and H. Schindler, MOTILITY AND REVERSIBLE INACTIVATION OF HONEYBEE SPERMATOZOA IN VIVO AND IN VITRO, Annales de l'Abeille, vol.10, issue.1, pp.5-16, 1967.
DOI : 10.1051/apido:19670101

URL : https://hal.archives-ouvertes.fr/hal-00890245

M. Lodesani, D. Balduzzi, and A. Galli, ) queen spermathecae, Journal of Apicultural Research, vol.43, issue.1, 2004.
DOI : 10.1051/apido:19780301

H. R. Mattila and T. D. Seeley, Genetic Diversity in Honey Bee Colonies Enhances Productivity and Fitness, Science, vol.52, issue.1, pp.362-364, 2007.
DOI : 10.1146/annurev.ento.46.1.413

C. Mayack and D. Naug, Energetic stress in the honeybee Apis mellifera from Nosema ceranae infection, Journal of Invertebrate Pathology, vol.100, issue.3, pp.185-188, 2009.
DOI : 10.1016/j.jip.2008.12.001

D. Miller, J. Summers, and S. Silber, Environmental versus genetic sex determination: a possible factor in dinosaur extinction?, Fertility and Sterility, vol.81, issue.4, pp.954-964, 2004.
DOI : 10.1016/j.fertnstert.2003.09.051

S. Misra, A. Singh, C. , H. R. Sharma, V. Reddy-mudiam et al., Identification of Drosophila-Based Endpoints for the Assessment and Understanding of Xenobiotic-Mediated Male Reproductive Adversities, Toxicological Sciences, vol.141, issue.1, pp.278-291, 2014.
DOI : 10.1093/toxsci/kfu125

R. F. Moritz, Intracolonial worker relationship and sperm competition in the honeybee (Apis mellifera L.), Experientia, vol.16, issue.4, pp.445-448, 1986.
DOI : 10.1080/0005772X.1958.11095028

L. Multigner, P. Kadhel, F. Rouget, P. Blanchet, and S. Cordier, Chlordecone exposure and adverse effects in French West Indies populations, Environmental Science and Pollution Research, vol.3, issue.6, pp.3-8, 2016.
DOI : 10.1080/15287398409530582

URL : https://hal.archives-ouvertes.fr/hal-01150382

C. M. Nelson and R. G. Bunge, Semen Analysis: Evidence for Changing Parameters of Male Fertility Potential, Fertility and Sterility, vol.25, issue.6, pp.503-507, 1974.
DOI : 10.1016/S0015-0282(16)40454-1

P. Neumann and N. Carreck, Honey bee colony losses, Journal of Apicultural Research, vol.49, issue.1, pp.1-6, 2010.
DOI : 10.3896/IBRA.1.49.1.20

URL : http://www.tandfonline.com/doi/pdf/10.3896/IBRA.1.49.1.01?needAccess=true

D. Nicodemo, M. A. Maioli, H. C. Medeiros, M. Guelfi, K. V. Balieira et al., Fipronil and imidacloprid reduce honeybee mitochondrial activity, Environmental Toxicology and Chemistry, vol.203, issue.9, pp.2070-2075, 2014.
DOI : 10.1007/BF00693012

A. Nieto, S. P. Roberts, J. Kemp, P. Rasmont, M. Kuhlmann et al., European Red List of bees, 2014.

B. P. Oldroyd, What's Killing American Honey Bees?, PLoS Biology, vol.33, issue.6, pp.1195-1199, 2007.
DOI : 10.1371/journal.pbio.0050168.t001

URL : https://doi.org/10.1371/journal.pbio.0050168

B. P. Oldroyd and J. H. Fewell, Large fitness benefits from polyandry in the honey bee, Apis mellifera, Trends in Ecology & Evolution, vol.23, issue.2, pp.59-60, 2008.
DOI : 10.1016/j.tree.2007.10.012

A. Oliva, A. Spira, and L. Multigner, Contribution of environmental factors to the risk of male infertility, Human Reproduction, vol.16, issue.8, pp.1768-1776, 2001.
DOI : 10.1093/humrep/16.8.1768

W. E. Olooto, A. Ambali, and T. A. Banjo, A review of female infertility: important etiological factors and management, J. Microbiol. Biotechnol. Res, vol.2, pp.379-385, 2012.

R. E. Page and C. Y. Peng, Aging and development in social insects with emphasis on the honey bee, Apis mellifera L., Experimental Gerontology, vol.36, issue.4-6, pp.4-6, 2001.
DOI : 10.1016/S0531-5565(00)00236-9

J. Pain, NOTE TECHNIQUE NOUVEAU MOD??LE DE CAGETTES EXP??RIMENTALES POUR LE MAINTIEN D'ABEILLES EN CAPTIVIT??, Annales de l'Abeille, vol.9, issue.1, pp.71-76, 1966.
DOI : 10.1051/apido:19660106

D. Pellati, I. Mylonakis, G. Bertoloni, C. Fiore, A. Andrisani et al., Genital tract infections and infertility, European Journal of Obstetrics & Gynecology and Reproductive Biology, vol.140, issue.1, pp.3-11, 2008.
DOI : 10.1016/j.ejogrb.2008.03.009

Y. Peng, B. Baer-imhoof, A. H. Millar, and B. Baer, Consequences of Nosema apis infection for male honey bees and their fertility, Scientific Reports, vol.9, issue.1, 2015.
DOI : 10.1002/pmic.200800708

R. Pigeault, J. Vezilier, A. Nicot, S. Gandon, and A. Rivero, Transgenerational effect of infection in Plasmodium-infected mosquitoes, Biology Letters, vol.279, issue.1746, 2015.
DOI : 10.1098/rspb.2012.1841

L. W. Pisa, V. Amaral-rogers, L. P. Belzunces, J. M. Bonmatin, C. A. Downs et al., Effects of neonicotinoids and fipronil on non-target invertebrates, Environmental Science and Pollution Research, vol.30, issue.425, pp.68-102, 1007.
DOI : 10.1016/j.cropro.2010.10.006

URL : https://hal.archives-ouvertes.fr/hal-01171771

S. G. Potts, J. C. Biesmeijer, C. Kremen, P. Neumann, O. Schweiger et al., Global pollinator declines: trends, impacts and drivers, Trends in Ecology & Evolution, vol.25, issue.6, pp.345-353, 2010.
DOI : 10.1016/j.tree.2010.01.007

URL : http://www.intertropi.ufam.edu.br/docs/ecosystem_services.pdf

F. L. Ratnieks and L. Keller, Queen control of egg fertilization in the honey bee, Behavioral Ecology and Sociobiology, vol.44, issue.1, pp.57-61, 1998.
DOI : 10.1007/s002650050514

J. Rhodes and D. Somerville, Introduction and Early Performance of Queen Bees: Some Factors Affecting Success : a Report for the Rural Industries Research and Development Corporation, Rural Industries Research and Development Corporation, 2003.

F. J. Richard, D. R. Tarpy, and C. M. Grozinger, Effects of Insemination Quantity on Honey Bee Queen Physiology, PLoS ONE, vol.302, issue.10, 2007.
DOI : 10.1371/journal.pone.0000980.t002

T. E. Rinderer, L. I. De-guzman, V. A. Lancaster, G. T. Delatte, and J. A. Stelzer, Varroa in the mating yard: I. The effects of Varroa jacobsoni and Apistan (R) on drone honey bees, Am. Bee J, vol.139, issue.2, pp.134-139, 1999.

K. E. Roberts, S. E. Evison, B. Baer, and W. O. Hughes, The cost of promiscuity: sexual transmission of Nosema microsporidian parasites in polyandrous honey bees, Scientific Reports, vol.39, issue.1, 2015.
DOI : 10.1051/apido:2008015

W. C. Roberts and O. Mackensen, Breeding improved honey bees, Am. Bee J, vol.91, pp.382-384, 1951.

E. Niemeier, L. Belhouchet, F. Bernardini, M. Budja, G. Cooney et al., Widespread exploitation of the honeybee by early Neolithic farmers, Nature, vol.527, issue.7577, pp.226-230, 1038.
URL : https://hal.archives-ouvertes.fr/hal-01433290

M. Rolland, L. Moal, J. Wagner, V. Royere, D. De-mouzon et al., Decline in semen concentration and morphology in a sample of 26 609 men close to general population between 1989 and 2005 in France, Human Reproduction, vol.28, issue.2, pp.462-470, 1989.
DOI : 10.1093/humrep/des415

URL : https://hal.archives-ouvertes.fr/hal-01129703

F. Ruttner, L'organe génital mâle et l'accouplement. Traité de Biologie de l, Abeille. R. Chauvin, pp.145-185, 1968.

F. Ruttner, The instrumental insemination of the queen bee, 1976.

F. Ruttner and G. Koeniger, The filling of the spermatheca of the honey bee queen, Zeitschrift f???r Vergleichende Physiologie, vol.4, issue.4, pp.411-421, 1971.
DOI : 10.1007/BF00300712

C. Sandrock, M. Tanadini, L. G. Tanadini, A. Fauser-misslin, S. G. Potts et al., Impact of Chronic Neonicotinoid Exposure on Honeybee Colony Performance and Queen Supersedure, PLoS ONE, vol.491, issue.8, 2014.
DOI : 10.1371/journal.pone.0103592.s001

H. Schluns, G. Koeniger, N. Koeniger, and R. F. Moritz, Sperm utilization pattern in the honeybee (Apis mellifera), Behavioral Ecology and Sociobiology, vol.22, issue.5, pp.458-463, 2004.
DOI : 10.1080/00218839.1983.11100578

H. Schluns, R. F. Moritz, H. M. Lattorff, and G. Koeniger, ), Apidologie, vol.36, issue.2, pp.201-209, 2005.
DOI : 10.1051/apido:2005006

H. Schluns, R. F. Moritz, P. Neumann, P. Kryger, and G. Koeniger, Multiple nuptial flights, sperm transfer and the evolution of extreme polyandry in honeybee queens, Animal Behaviour, vol.70, issue.1, pp.125-131, 2005.
DOI : 10.1016/j.anbehav.2004.11.005

H. Schluns, E. A. Schluns, J. Van-praagh, and R. F. Moritz, ) depend on body size, Apidologie, vol.34, issue.6, pp.577-584, 2003.
DOI : 10.1051/apido:2003051

T. D. Seeley, P. K. Visscher, and K. M. Passino, Group decision making in honey bee swarms, Am. Sci, vol.94, issue.3, pp.220-229, 2006.

N. Seitz, K. S. Traynor, N. Steinhauer, K. Rennich, M. E. Wilson et al., A national survey of managed honey bee 2014???2015 annual colony losses in the USA, Journal of Apicultural Research, vol.147, issue.4, pp.292-304, 1080.
DOI : 10.1017/s003118200600710

R. K. Seth, J. J. Kaur, D. K. Rao, and S. E. Reynolds, Effects of larval exposure to sublethal concentrations of the ecdysteroid agonists RH-5849 and tebufenozide (RH-5992) on male reproductive physiology in Spodoptera litura, Journal of Insect Physiology, vol.50, issue.6, 2004.
DOI : 10.1016/j.jinsphys.2004.03.007

S. Shafir, L. Kabanoff, M. Duncan, and B. P. Oldroyd, ) sperm competition in vitro ??? two are no less viable than one, Apidologie, vol.22, issue.5, pp.556-561, 2009.
DOI : 10.1080/00218839.1983.11100579

R. M. Sharpe and D. S. Irvine, How strong is the evidence of a link between environmental chemicals and adverse effects on human reproductive health?, BMJ, vol.328, issue.7437, pp.447-451, 2004.
DOI : 10.1136/bmj.328.7437.447

R. M. Sharpe and N. E. Skakkebaek, Are oestrogens involved in falling sperm counts and disorders of the male reproductive tract?, The Lancet, vol.341, issue.8857, pp.341-1392, 1993.
DOI : 10.1016/0140-6736(93)90953-E

N. Simon-delso, V. Amaral-rogers, L. P. Belzunces, J. M. Bonmatin, M. Chagnon et al., Systemic insecticides (neonicotinoids and fipronil): trends, uses, mode of action and metabolites, Environmental Science and Pollution Research, vol.59, issue.6133, pp.5-34, 1007.
DOI : 10.1021/jf102765x

URL : https://hal.archives-ouvertes.fr/hal-01171969

R. Slama and H. Leridon, La fertilité humaine : approches épidémiologique et démographique. La reproduction animale et humaine. M. Saint-Dizier and S. Chastant- Maillard, pp.487-506, 2014.

I. Steffan-dewenter and A. Kuhn, Honeybee foraging in differentially structured landscapes, Proceedings of the Royal Society B: Biological Sciences, vol.270, issue.1515, pp.569-575, 1515.
DOI : 10.1098/rspb.2002.2292

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1691282/pdf

L. Straub, L. Villamar-bouza, S. Bruckner, P. Chantawannakul, L. Gauthier et al., Neonicotinoid insecticides can serve as inadvertent insect contraceptives, Proceedings of the Royal Society B: Biological Sciences, vol.44, issue.4, 1835.
DOI : 10.1007/s13592-013-0199-4

URL : http://rspb.royalsocietypublishing.org/content/royprsb/283/1835/20160506.full.pdf

J. P. Sumpter, Endocrine Disruption in the Aquatic Environment, Endocrine Disruptors ? Part II. M. Metzler. Berlin, pp.271-289, 2002.
DOI : 10.1007/10833691_10

L. W. Sun, R. Jin, Z. H. Peng, Q. W. Zhou, H. F. Qian et al., Effects of trilostane and fipronil on the reproductive axis in an early life stage of the Japanese medaka (Oryzias latipes), Ecotoxicology, vol.42, issue.21, pp.1044-1054, 2014.
DOI : 10.1021/es801573x

T. I. Szabo and D. T. Heikel, Numbers of Spermatozoa in Spermathecae of Queens Aged 0 to 3 Years Reared in Beaverlodge, Alberta, Journal of Apicultural Research, vol.8, issue.2, pp.79-82, 1987.
DOI : 10.1080/00218839.1971.11099669

D. R. Tarpy, Genetic diversity within honeybee colonies prevents severe infections and promotes colony growth, Proceedings of the Royal Society B: Biological Sciences, vol.270, issue.1510, pp.99-103, 1510.
DOI : 10.1098/rspb.2002.2199

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1691209/pdf

D. R. Tarpy, J. J. Keller, J. R. Caren, and D. A. Delaney, Assessing the Mating ???Health??? of Commercial Honey Bee Queens, Journal of Economic Entomology, vol.105, issue.1, pp.20-25, 2012.
DOI : 10.1603/EC11276

D. R. Tarpy and R. E. Page, Sex determination and the evolution of polyandry in honey bees ( Apis mellifera ), Behavioral Ecology and Sociobiology, vol.52, issue.2, pp.143-150, 2002.
DOI : 10.1007/s00265-002-0498-7

K. T. Tassou and R. Schulz, Low field-relevant tebufenozide concentrations affect reproduction in Chironomus riparius (Diptera: Chironomidae) in a long-term toxicity test, Environmental Science and Pollution Research, vol.105, issue.436, pp.3735-3742, 2013.
DOI : 10.1126/science.241.4864.470

A. Tofilski, A scientific note on amoeboid movement of honey bee semen, Apidologie, vol.44, issue.5, 2014.
DOI : 10.1051/apido:19780301

URL : https://hal.archives-ouvertes.fr/hal-01234749

A. Tofilski, B. Chuda-mickiewicz, K. Czeko?ska, and P. Chorbi?ski, Flow cytometry evidence about sperm competition in honey bee (Apis mellifera), Apidologie, vol.39, issue.1, pp.63-70, 2012.
DOI : 10.1080/0005772X.1958.11095028

URL : https://hal.archives-ouvertes.fr/hal-01003627

D. Vanengelsdorp, J. Hayes, R. M. Underwood, and J. Pettis, A survey of Honey Bee colony losses in the US, Fall 2007 to Spring, PLoS One, vol.3, issue.12, 2008.

D. Vanengelsdorp and M. D. Meixner, A historical review of managed honey bee populations in Europe and the United States and the factors that may affect them, Journal of Invertebrate Pathology, vol.103, 2010.
DOI : 10.1016/j.jip.2009.06.011

L. R. Verma, BIOLOGY OF HONEYBEE (APIS MELLIFERA L.) SPERMATOZOA. 1. Effect of different diluents on motility and survival, Apidologie, vol.9, issue.3, pp.167-173, 1978.
DOI : 10.1051/apido:19780301

URL : https://hal.archives-ouvertes.fr/hal-00890462

L. R. Verma, Biology of Honeybee Spermatozoa 2. Effect of Washing and of Sugars on Respiration as Measured by the Cartesian Diver Technique, Journal of Apicultural Research, vol.30, issue.4, pp.176-181, 1978.
DOI : 10.1016/0022-1910(73)90225-4

L. R. Verma, BIOLOGY OF HONEYBEE SPERMATOZOA. 3. EFFECT OF AMINO ACIDS AND CATALASE ON RESPIRATION AS MEASURED BY THE CARTESIAN DIVER TECHNIQUE, Apidologie, vol.12, issue.4, pp.377-382, 1981.
DOI : 10.1051/apido:19810406

URL : https://hal.archives-ouvertes.fr/hal-00890462

L. R. Verma and R. W. Shuel, Respiratory metabolism of the semen of the honey-bee, Apis mellifera, Journal of Insect Physiology, vol.19, issue.1, pp.97-103, 1973.
DOI : 10.1016/0022-1910(73)90225-4

L. R. Verma and R. W. Shuel, Respiratory metabolism of the semen of the honey-bee, Apis mellifera, Journal of Insect Physiology, vol.19, issue.1, pp.97-103, 1973.
DOI : 10.1016/0022-1910(73)90225-4

C. Vidau, J. Brunet, A. Badiou, and L. P. Belzunces, Phenylpyrazole insecticides induce cytotoxicity by altering mechanisms involved in cellular energy supply in the human epithelial cell model Caco-2, Toxicology in Vitro, vol.23, issue.4, pp.589-597, 2009.
DOI : 10.1016/j.tiv.2009.01.017

C. Vidau, M. Diogon, J. Aufauvre, R. Fontbonne, B. Vigues et al., Exposure to Sublethal Doses of Fipronil and Thiacloprid Highly Increases Mortality of Honeybees Previously Infected by Nosema ceranae, PLoS ONE, vol.78, issue.6, 2011.
DOI : 10.1371/journal.pone.0021550.g004

URL : https://hal.archives-ouvertes.fr/hal-00814778

C. Vidau, R. A. Gonzalez-polo, M. Niso-santano, R. Gomez-sanchez, J. M. Bravo-san-pedro et al., Fipronil is a powerful uncoupler of oxidative phosphorylation that triggers apoptosis in human neuronal cell line SHSY5Y, NeuroToxicology, vol.32, issue.6, pp.935-943, 2011.
DOI : 10.1016/j.neuro.2011.04.006

X. Wang, M. A. Martinez, Q. Wu, I. Ares, M. R. Martinez-larranaga et al., Fipronil insecticide toxicology: oxidative stress and metabolism, Critical Reviews in Toxicology, vol.33, issue.10, pp.1-24, 2016.
DOI : 10.1021/jf505916f

J. Wegener, H. Ruhnke, K. Milchreit, K. Kleebaum, M. Franke et al., Secondary biomarkers of insecticide-induced stress of honey bee colonies and their relevance for overwintering strength, Ecotoxicology and Environmental Safety, vol.132, 2016.
DOI : 10.1016/j.ecoenv.2016.06.038

B. A. Williams, Unique physiology of host-parasite interactions in microsporidia infections, Cellular Microbiology, vol.50, issue.1, pp.1551-1560, 2009.
DOI : 10.1128/9781555818227.ch5

G. R. Williams, A. Troxler, G. Retschnig, K. Roth, O. Yañez et al., Neonicotinoid pesticides severely affect honey bee queens, Scientific Reports, vol.23, 2015.
DOI : 10.3896/IBRA.1.52.4.13

URL : http://www.nature.com/articles/srep14621.pdf

W. T. Wilson and D. M. Menapace, Disappearing disease of honey bees: a survey of the United States, Am. Bee J, vol.119, issue.3, pp.184-186, 1979.

M. L. Winston, The Biology of the Honeybee, 1987.

J. Woyke, Natural and Artificial Insemination of Queen Honeybees, Bee World, vol.43, issue.1, pp.21-25, 1962.
DOI : 10.1080/0005772X.1962.11096922

J. Woyke, Effect of the Access of Worker Honeybees to the Queen on the Results of Instrumental Insemination, Journal of Apicultural Research, vol.18, issue.3, pp.136-143, 1979.
DOI : 10.1051/apido:19760402

J. Woyke, Dynamics of Entry of Spermatozoa into the Spermatheca of Instrumentally inseminated Queen Honeybees, Journal of Apicultural Research, vol.22, issue.3, pp.150-154, 1983.
DOI : 10.1051/apido:19790205

J. Woyke, Ultrastructure of Single and Multiple Diploid Honeybee Spermatozoa, Journal of Apicultural Research, vol.4, issue.3, 1984.
DOI : 10.1080/00218839.1974.11099777

J. Woyke, Sex Determination, Bee Genetics and Breeding. T. E. Rinderer, pp.91-119, 1986.
DOI : 10.1016/B978-0-12-588920-9.50009-1

J. Woyke and Z. Jasinski, INFLUENCE OF THE NUMBER OF ATTENDANT WORKERS ON THE RESULTS OF INSTRUMENTAL INSEMINATION OF HONEYBEE QUEENS KEPT AT ROOM TEMPERATURE, Apidologie, vol.11, issue.2, 1980.
DOI : 10.1051/apido:19800207

URL : https://hal.archives-ouvertes.fr/hal-00890520

D. Xiao, T. Yang, N. Desneux, P. Han, and X. Gao, Assessment of Sublethal and Transgenerational Effects of Pirimicarb on the Wheat Aphids Rhopalosiphum padi and Sitobion avenae, PLOS ONE, vol.33, issue.6, 2015.
DOI : 10.1371/journal.pone.0128936.t005

R. L. Yu and S. W. Omholt, Early developmental processes in the fertilised honeybee (Apis mellifera) oocyte, Journal of Insect Physiology, vol.45, issue.8, pp.763-767, 1999.
DOI : 10.1016/S0022-1910(99)00056-6

C. Yue, M. Schröder, S. Gisder, and E. Genersch, Vertical-transmission routes for deformed wing virus of honeybees (Apis mellifera), Journal of General Virology, vol.88, issue.8, pp.2329-2336, 2007.
DOI : 10.1099/vir.0.83101-0