User menu

Accès à distance ? S'identifier sur le proxy UCLouvain

Consequence of emergence pattern on inbreeding risk in the aphid parasitoid Aphidius matricariae (Hymenoptera: Braconidae)

Primary tabs

download
  • Open access
  • PDF
  • 1.62 M
Bourdais, Delphine [UCL] Hance, Thierry [UCL]

In insect parasitoids, mating strategy depends on mate availability and is influenced by the spatial and temporal emergence patterns of adults. For quasi-gregarious species, simultaneous emergence favors local mating and reduces search costs for partners while increasing the risk of inbreeding, particularly when only one female parasitizes the initial host patch. Consequently, in inbreeding sensitive species, mating on the place of adult emergence (patch mating) between siblings should be counter selected. In practice, the timing of male and female emergence and of their dispersal influences mate availability and can limit on patch mating. To test the role of these two factors, we analyzed the daily distribution of emergence and patch residence time of a cohort in the aphid parasitoid Aphidius matricariae (Hymenoptera: Braconidae). We observed that adult emergence is concentrated on the morning with males emerging on average before females with some overlaps. A more precise evaluation of emergence pattern within a brood suggests that brothers and sisters rarely emerge at the same time and rapid dispersal of males and females favors off-patch mating. The relationships between timing of emergence including differences between sex and consequences on inbreeding probability in these species are thus discussed.

Document type Article de périodique (Journal article) – Article de recherche
Access type Accès libre
Publication date 2019
Language Anglais
Journal information "Chronobiology International" - Vol. 36, no. 6, p. 838–850 (2019)
Peer reviewed yes
Publisher Informa Healthcare (London)
issn 0742-0528
e-issn 1525-6073
Publication status Publié
Affiliation UCL - SST/ELI/ELIB - Biodiversity
Keywords Physiology (medical) ; Physiology ; Pharmacology ; Mate availability ; protandry ; local mate competition ; timing of emergence ; post emergence dispersal ; inbreeding avoidance
Links
  1. BATTAGLIA Donatella, ISIDORO Nunzio, ROMANI Roberto, BIN Ferdinando, PENNACHIO Francesco, Mating behaviour of Aphidius ervi (Hymenoptera: Braconidae): The role of antennae, 10.14411/eje.2002.057
  2. Beck Stanley D., Thermoperiodism, Insects at Low Temperature (1991) ISBN:9781475701920 p.199-228, 10.1007/978-1-4757-0190-6_9
  3. Bertossa Rinaldo C., van Dijk Jeroen, Beersma Domien G., Beukeboom Leo W., Circadian rhythms of adult emergence and activity but not eclosion in males of the parasitic wasp Nasonia vitripennis, 10.1016/j.jinsphys.2010.02.008
  4. Boivin G, Ann Soc Entomol Fr, 35, 371 (1999)
  5. Boulton Rebecca A., Collins Laura A., Shuker David M., Beyond sex allocation: the role of mating systems in sexual selection in parasitoid wasps : Sexual selection in parasitoid wasps, 10.1111/brv.12126
  6. Bourdais D., Hance T., Lack of behavioural evidence for kin avoidance in mate choice in a hymenopteran parasitoid (Hymenoptera: Braconidae), 10.1016/j.beproc.2009.02.015
  7. Brodeur Jacques, Rosenheim Jay A., Intraguild interactions in aphid parasitoids, 10.1046/j.1570-7458.2000.00720.x
  8. Cook James M, Crozier Ross H, Sex determination and population biology in the hymenoptera, 10.1016/0169-5347(95)90011-x
  9. Copeland Robert A., Enzymes, ISBN:0471359297, 10.1002/0471220639
  10. Corrigan J. E., Laing J. E., Zubricky J. S., Effects of Parasitoid to Host Ratio and Time of Day of Parasitism on Development and Emergence of Trichogramma minutum (Hymenoptera: Trichogrammatidae) Parasitizing Eggs of Ephestia kuehniella (Lepidoptera: Pyralidae), 10.1093/aesa/88.6.773
  11. Doyon Josée, Boivin Guy, The effect of development time on the fitness of female Trichogramma evanescens, 10.1093/jis/5.1.4
  12. Doyon Josée, Boivin Guy, Impact of the Timing of Male Emergence on Mating Capacity of Males in Trichogramma evanescens Westwood, 10.1007/s10526-006-9001-0
  13. ELIAS J., DORN S., MAZZI D., Inbreeding in a natural population of the gregarious parasitoid wasp Cotesia glomerata : INBREEDING IN A PARASITOID WASP, 10.1111/j.1365-294x.2010.04645.x
  14. Fantinou A.A., Alexandri M.P., Tsitsipis J.A., 10.1023/a:1009984318289
  15. Fauvergue Xavier, Fleury Frederic, Lemaitre Claire, Allemand Rolland, Parasitoid Mating Structures When Hosts Are Patchily Distributed: Field and Laboratory Experiments with Leptopilina boulardi and L. heterotoma, 10.2307/3546451
  16. Giebultowicz Jadwiga M, Insect circadian clocks: is it all in their heads?, 10.1016/s0022-1910(99)00055-4
  17. Giri M. K., Pass B. C., Yeargan K. V., Parr J. C., Behavior, net reproduction, longevity, and mummy-stage survival ofAphidius matricariae [Hym. Aphidiidae], 10.1007/bf02375222
  18. Godfray HCJ, Parasitoids: behavioural and evolutionary ecology (1994)
  19. Godfray H. C. J., Cook J. M., Mating systems of parasitoid wasps, The Evolution of Mating Systems in Insects and Arachnids ISBN:9780511721946 p.211-225, 10.1017/cbo9780511721946.013
  20. Greeff J. M., Alternative mating strategies, partial sibmating and split sex ratios in haplodiploid species, 10.1046/j.1420-9101.1996.9060855.x
  21. Hagvar EB, Biocontrol News Inf, 12, 13 (1991)
  22. Hamilton W. D., Extraordinary Sex Ratios, 10.1126/science.156.3774.477
  23. Hance T., Kohandani-Tafresh F., Munaut F., Biological control., Aphids as crop pests ISBN:9781780647098 p.448-493, 10.1079/9781780647098.0448
  24. Hance Thierry, van Baaren Joan, Vernon Philippe, Boivin Guy, Impact of Extreme Temperatures on Parasitoids in a Climate Change Perspective, 10.1146/annurev.ento.52.110405.091333
  25. He Xiong Zhao, Wang Qiao, Reproductive strategies of Aphidius ervi Haliday (Hymenoptera: Aphidiidae), 10.1016/j.biocontrol.2008.03.003
  26. He XZ, N Z Plant Prot, 57, 214 (2004)
  27. Heimpel George E., de Boer Jetske G., Sex Determination in the Hymenoptera, 10.1146/annurev.ento.53.103106.093441
  28. Helfrich-Förster Charlotte, The locomotor activity rhythm of Drosophila melanogaster is controlled by a dual oscillator system, 10.1016/s0022-1910(01)00060-9
  29. Hirose Yoshimi, Vinson S. B., Hirose Yasuko, Protandry in the parasitoid Cardiochiles nigriceps , as related to its mating system, 10.1007/bf02348581
  30. Karpova SG, Ent Rev, 86, 267 (2006)
  31. KARPOVA Svetlana G., REZNIK Sergey Ya., Interaction of exogenous factors (light and temperature) in their influence on the daily pattern of adult eclosion in Trichogramma embryophagum (Hymenoptera: Trichogrammatidae), 10.14411/eje.2002.054
  32. Lankinen Pekka, Geographical variation in circadian eclosion rhythm and photoperiodic adult diapause inDrosophila littoralis, 10.1007/bf00612503
  33. Le Ralec Anne, Anselme Caroline, Outreman Yannick, Poirié Marylène, van Baaren Joan, Le Lann Cécile, van Alphen Jacques J.-M., Evolutionary ecology of the interactions between aphids and their parasitoids, 10.1016/j.crvi.2010.03.010
  34. Mackauer M, World Aphidiidae (1967)
  35. Martel V., Boivin G., Premating Dispersion in the Egg ParasitoidTrichogramma(Hymenoptera: Trichogrammatidae), 10.1603/0046-225x-33.4.855
  36. MARTEL VÉRONIQUE, DOYON JOSÉE, BOIVIN GUY, Partial local mate competition in the wasp Trichogramma euproctidis: the role of emergence sex ratio on female mating behaviour, 10.1111/j.1365-2311.2010.01229.x
  37. MAZZI DOMINIQUE, HATT FABIENNE, HEIN SILKE, DORN SILVIA, Ladies last: diel rhythmicity of adult emergence in a parasitoid with complementary sex determination, 10.1111/j.1365-3032.2010.00761.x
  38. MOller Anders Pape, Protandry, sexual selection and climate change, 10.1111/j.1365-2486.2004.00874.x
  39. Morbey Yolanda E., Ydenberg Ronald C., Protandrous arrival timing to breeding areas: a review, 10.1046/j.1461-0248.2001.00265.x
  40. Myers Edith M., The Circadian Control of Eclosion, 10.1081/cbi-120024214
  41. Nunes Marlies Vaz, Saunders David, Photoperiodic Time Measurement in Insects: A Review of Clock Models, 10.1177/074873049901400202
  42. Pittendrigh C. S., Circadian systems. I. The driving oscillation and its assay in Drosophila pseudoobscura., 10.1073/pnas.58.4.1762
  43. Pompanon Francois, Fouillet Pierre, Bouletr�au Michel, Emergence rhythms and protandry in relation to daily patterns of locomotor activity inTrichogramma species, 10.1007/bf01237829
  44. REZNIK Sergey Ya., VOINOVICH Natalia D., VAGHINA Nina P., KARPOVA Svetlana G., Arrhythmic adult ecdysis but rhythmic emergence from the host chorion in Trichogramma embryophagum (Hymenoptera: Trichogrammatidae), 10.14411/eje.2008.011
  45. Rounbehler M. D., Ellington J. J., Some Biological Effects of Selected Light Regimes on Trichogramma semifumatum (Hymenoptera: Trichogrammatidae)1, 10.1093/aesa/66.1.6
  46. Sakai T., Ishida N., Circadian rhythms of female mating activity governed by clock genes in Drosophila, 10.1073/pnas.151443298
  47. Salin C, Belg J Zool, 134, 15 (2004)
  48. SAUNDERS DAVID S., Circadian rhythms and the evolution of photoperiodic timing in insects, 10.1111/j.1365-3032.2009.00699.x
  49. Shaffer Phillip L., Prediction of Variation in Development Period of Insects and Mites Reared at Constant Temperatures1, 10.1093/ee/12.4.1012
  50. Skopik S. D., Pittendrigh C. S., Circadian systems, II. The oscillation in the individual Drosophila pupa; its independence of developmental stage., 10.1073/pnas.58.5.1862
  51. Smith Sandy M., Biological Control with Trichogramma: Advances, Successes, and Potential of Their Use, 10.1146/annurev.en.41.010196.002111
  52. Steel CGH, Comprehensive insect physiology, pharmacology and biochemistry. Endocrinology II, 8, 1 (2013)
  53. Tauber Eran, Kyriacou Charalambos P., Molecular Evolution and Population Genetics of Circadian Clock Genes, Methods in Enzymology (2005) ISBN:9780121827984 p.797-817, 10.1016/s0076-6879(05)93042-5
  54. Tentelier Cédric, Desouhant Emmanuel, Fauvergue Xavier, Habitat assessment by parasitoids: mechanisms for patch use behavior, 10.1093/beheco/arj062
  55. Lenteren J. C. van, Szabo P., Huisman P. W. T., The parasite-host relationship betweenEncarsia formosaGahan (Hymenoptera, Aphelinidae) andTrialeurodes vaporariorum(Westwood) (Homoptera, Aleyrodidae), 10.1111/j.1439-0418.1992.tb01142.x
  56. Wajnberg Éric, Time allocation strategies in insect parasitoids: from ultimate predictions to proximate behavioral mechanisms, 10.1007/s00265-006-0198-9
  57. Wedell Nina, Protandry and mate assessment in the wartbiter Decticus verrucivorus (Orthoptera : Tettigoniidae), 10.1007/bf00177770
  58. WERREN J. H., Sex Ratio Adaptations to Local Mate Competition in a Parasitic Wasp, 10.1126/science.208.4448.1157
  59. Wiklund Christer, Fagerstr�m Torbj�rn, Why do males emerge before females? : A hypothesis to explain the incidence of protandry in butterflies, 10.1007/bf00346917
  60. Zamani Abbas Ali, Talebi Aliasghar, Fathipour Yaghoub, Baniameri Valiollah, Effect of Temperature on Life History of Aphidius colemani and Aphidius matricariae (Hymenoptera: Braconidae), Two Parasitoids of Aphis gossypii and Myzus persicae (Homoptera: Aphididae), 10.1603/0046-225x-36.2.263
  61. Zaslavski VA, Entomol Rev, 79, 1 (1999)
  62. Zaviezo Tania, Retamal Romina, Urvois Teddy, Fauvergue Xavier, Blin Aurélie, Malausa Thibaut, Effects of inbreeding on a gregarious parasitoid wasp with complementary sex determination, 10.1111/eva.12537
  63. Zijlstra WG, Evol Ecol Res, 4, 1229 (2002)
  64. Zonneveld C., Sperm Competition Cannot Eliminate Protandry, 10.1006/jtbi.1996.0010
  65. Zonneveld C., Metz J.A.J., Models on butterfly protandry: Virgin females are at risk to die, 10.1016/0040-5809(91)90058-n
Bibliographic reference Bourdais, Delphine ; Hance, Thierry. Consequence of emergence pattern on inbreeding risk in the aphid parasitoid Aphidius matricariae (Hymenoptera: Braconidae). In: Chronobiology International, Vol. 36, no. 6, p. 838–850 (2019)
Permanent URL http://hdl.handle.net/2078.1/215108