A. Dixon, Aphid Ecology, 1998.

L. Trionnaire, G. Hardie, J. Jaubert-possamai, S. Simon, J. Tagu et al., Shifting from asexual to sexual reproduction in aphids: physiological and developmental aspects, Biol Cell, vol.100, pp.441-451, 2008.

A. D. Lees, The role of photoperiod and temperature in the determination of parthenogenetic and sexual forms in the aphid Megoura viciae Buckton -I. The influence of these factors on apterous virginoparae and their progeny, J Ins Physiol, vol.3, pp.92-117, 1959.

A. D. Lees, Photoperiodic time measurement in the aphid Megoura viciae, J Ins Physiol, vol.19, pp.2279-2316, 1973.

A. D. Lees, Action spectra for the photoperiodic control of polymorphism in the aphid Megoura viciae, J Ins Physiol, vol.27, pp.761-771, 1981.

J. Hardie, A. D. Lees, and S. Young, Light transmission through the head capsule of an aphid, Megoura viciae, J Ins Physiol, vol.27, pp.773-777, 1981.

N. Gao, M. Von-schantz, R. G. Foster, and J. Hardie, The putative brain photoperiodic photoreceptors in the vetch aphid, Megoura viciae, J Ins Physiol, vol.45, pp.1011-1019, 1999.

C. Steel and A. D. Lees, The role of neurosecretion in the photoperiodic control of polymorphism in the aphid Megoura viciae, J Exp Biol, vol.67, pp.117-135, 1977.

N. Gao and J. Hardie, Melatonin and the pea aphid, Acyrthosiphon pisum, J Ins Physiol, vol.43, pp.615-620, 1997.

J. Hardie, A. D. Lees, G. A. Kerhut, and G. L. Oxford, Endocrine control of polymorphism and polyphenism, Comprehensive insect physiology, vol.8, pp.441-490

J. Hardie, Juvenile hormone stimulation of oocyte development and embryogenesis in the parthenogenetic ovaries of an aphid, Aphis fabae, Int J Invert Reprod Dev, vol.11, pp.189-202, 1987.

J. A. Brisson and D. L. Stern, The pea aphid, Acyrthosiphon pisum : an emerging genomic model system for ecological, developmental and evolutionary studies, BioEssays, vol.28, pp.747-755, 2006.

D. Tagu, J. P. Klingler, A. Moya, and J. Simon, Early progress in aphid genomics and consequences for plant-aphid interactions studies, Mol Plant Microb Interac, vol.6, pp.701-708, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02655362

S. Ramos, A. Moya, and D. Martinez-torres, Identification of a gene overexpressed in aphids reared under short photoperiod, Ins Biochem Mol Biol, vol.33, pp.289-298, 2003.

L. Trionnaire, G. Jaubert, S. Sabater-munoz, B. Benedetto, A. Bonhomme et al., Seasonal photoperiodism regulates the expression of cuticular and signalling protein genes in the pea aphid, Ins Biochem Mol Biol, vol.37, pp.1094-1102, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02656485

T. Cortes, D. Tagu, J. C. Simon, A. Moya, and D. Martínez-torres, Sex versus parthenogenesis: A transcriptomic approach of photoperiod response in the model aphid Acyrthosiphon pisum (Hemiptera: Aphididae), vol.408, pp.146-156, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02663331

A. D. Lees, The location of the photoperiodic receptors in the aphid Megoura viciae Buckton, J Exp Biol, vol.41, pp.119-133, 1964.

Y. S. Zhong, K. Mita, T. Shimada, and H. Kawasaki, Glycine-rich protein genes, which encode a major component of the cuticle, have different developmental profiles from other cuticle protein genes in Bombyx mori, Ins Biochem Mol Biol, vol.36, pp.99-110, 2006.

S. O. Andersen, Studies on proteins in post-ecdysial nymphal cuticle of locust, Locusta migratoria, and cockroach, vol.30, pp.569-577, 2000.

C. K. Magkrioti, I. C. Spyropoulos, V. A. Iconomidou, and J. H. Willis, Hamodrakas SJ: cuticleDB: a relational database of Arthropod cuticular proteins, BMC Bioinf, vol.5, p.138, 2004.

A. D. Lees, The photoperiodic responses and phenology of an English strain of the pea aphid Acyrthosiphon pisum, Ecol Entomol, vol.14, pp.69-78, 1989.

E. E. Rosenbaum, R. C. Hardie, and N. J. Colley, Calnexin is essential for rhodopsin maturation, Ca2+ regulation, and photoreceptor cell survival, Neuron, vol.49, pp.229-241, 2006.

S. J. Lee, H. Xu, L. W. Kang, L. M. Amzel, and C. Montell, Light adaptation through phosphoinositide-regulated translocation of Drosophila visual arrestin, Neuron, vol.39, pp.121-132, 2003.

S. Shiga and H. Numata, Neuroanatomical approaches to the study of insect photoperiodism, Photochem Photobiol, vol.83, pp.76-86, 2007.

K. Babu, S. Bahri, L. Alphey, and W. Chia, Bifocal and PP1 interaction regulates targeting of the R-cell growth cone in Drosophila, Dev Biol, vol.288, pp.372-386, 2005.

A. M. Phillips, R. Smart, R. Strauss, B. Brembs, and L. E. Kelly, The Drosophila black enigma: The molecular characterization of the black ' mutant and behavioural allele, Gene, vol.351, pp.131-142, 2005.

J. Borycz, J. A. Borycz, and M. Loubani, Meinertzhagen IA: tan and ebony genes regulate a novel pathway for transmitter metabolism at fly photoreceptor terminals, J Neurosci, vol.22, pp.10549-10557, 2002.

R. J. Suderman, N. T. Dittmer, M. R. Kanost, and K. J. Kramer, Model reactions for insect cuticle sclerotization: Cross-linking of recombinant cuticular proteins upon their laccase-catalyzed oxidative conjugation with catechols, Ins Biochem Mol Biol, vol.36, pp.610-611, 2006.

J. Hardie, Nervous system. In Aphids, their Biology, vol.2, pp.131-138, 1987.

J. L. Fritz and M. Vanberkum, Regulation of Rho family GTPases is required to prevent axons from crossing the midline, Dev Biol, vol.252, pp.46-58, 2002.

D. Sanchez, M. D. Ganfornina, S. Torres-schumann, S. D. Speese, J. M. Lora et al., Characterization of two novel lipocalins expressed in the Drosophila embryonic nervous system, Int J Dev Biol, vol.44, pp.349-359, 2000.

Z. Wills, M. Emerson, J. Rusch, J. Bikoff, B. Baum et al., Van Vactor D: A Drosophila homolog of cyclase-associated proteins collaborates with the Abl tyrosine kinase to control midline axon pathfinding, Neuron, vol.36, pp.611-622, 2002.

J. M. Shulman and M. B. Feany, Genetic modifiers of tauopathy in Drosophila, Genetics, vol.165, pp.1233-1242, 2003.

R. Kraut, K. Menon, and K. Zinn, A gain-of-function screen for genes controlling motor axon guidance and synaptogenesis in Drosophila, Curr Biol, vol.11, pp.417-430, 2001.

C. C. Quattrocchi, F. Wannenes, A. M. Persico, S. A. Ciafre, D. 'arcangelo et al., Reelin is a serine protease of the extracellular matrix, J Biol Chem, vol.277, pp.303-309, 2002.

T. E. Lloyd, P. Verstreken, E. J. Ostrin, A. Phillippi, O. Lichtarge et al., A genome-wide search for synaptic vesicle cycle proteins in Drosophila, Neuron, vol.26, pp.45-50, 2000.

A. Kovoor, P. Seyffarth, J. Ebert, S. Barghshoon, C. K. Chen et al., D-2 dopamine receptors colocalize regulator of G-protein signaling 9-2 (RGS9-2) via the RGS9 DEP domain, and RGS9 knock-out mice develop dyskinesias associated with dopamine pathways, J Neurosci, vol.25, pp.2157-2165, 2005.

A. D. Lees, R. Downer, and N. Laufer, The endocrine control of polymorphism in aphids, Endocrinology of, pp.369-377, 1983.

M. P. Tu, C. M. Yin, and M. Tatar, Mutations in insulin signaling pathway alter juvenile hormone synthesis in Drosophila melanogaster, Gen Comp Endocrinol, vol.142, pp.347-356, 2005.

C. Sim and D. L. Denlinger, Insulin signaling and FOXO regulate the overwintering diapause of the mosquito Culex pipiens, Proc Natl Acad Sci, vol.105, pp.6777-6781, 2008.

S. A. Ament, M. Corona, H. S. Pollock, and G. E. Robinson, Insulin signaling is involved in the regulation of worker division of labor in honey bee colonies, Proc Nat Acad Sci, vol.105, pp.4226-4231, 2008.

B. Sabater-munõz, F. Legeai, C. Rispe, J. Bonhomme, P. Dearden et al., Tagu D: Large-scale gene discovery in the pea aphid Acyrthosiphon pisum (Hemiptera)

, Genome Biol, vol.7, p.21, 2006.

C. Figueroa, N. Prunier-leterme, C. Rispe, F. Sepúlveda, E. Fuentes-contreras et al., Annotated expressed sequence tags and xenobiotic detoxification in the aphid crop pest Myzus persicae, Ins Sci, vol.14, pp.29-45, 2007.

L. Meur, N. Lamirault, G. Bihouee, A. Steenman, M. Bedrine-ferran et al., A dynamic, web-accessible resource to process raw microarray scan data into consolidated gene expression values: importance of replication, Nucl Ac Res, vol.32, pp.5349-5358, 2004.

V. G. Tusher, R. Tibshirani, and G. Chu, Significance analysis of microarrays applied to the ionizing radiation response, Proc Nat Acad Sci, vol.98, pp.5116-5121, 2001.

F. Al-shahrour, J. Carbonell, P. Minguez, S. Goetz, A. Conesa et al.,