User menu

Differentiation in putative male sex pheromone components across and within populations of the African butterfly Bicyclus anynana as a potential driver of reproductive isolation

Bibliographic reference Bacquet, Paul ; de Jong, Maaike, A. ; Wang, Hong-Lei ; Molleman, Freerk ; Heuskin, Stéphanie ; et. al. Differentiation in putative male sex pheromone components across and within populations of the African butterfly Bicyclus anynana as a potential driver of reproductive isolation. In: Ecology and Evolution, (2016)
Permanent URL http://hdl.handle.net/2078.1/175095
  1. Aduse-Poku, Afr. J. Ecol., 50, 326 (2012)
  2. Allender C. J., Seehausen O., Knight M. E., Turner G. F., Maclean N., Divergent selection during speciation of Lake Malawi cichlid fishes inferred from parallel radiations in nuptial coloration, 10.1073/pnas.2332665100
  3. AMÉZQUITA ADOLFO, LIMA ALBERTINA P., JEHLE ROBERT, CASTELLANOS LINA, RAMOS ÓSCAR, CRAWFORD ANDREW J., GASSER HERBERT, HÖDL WALTER, Calls, colours, shape, and genes: a multi-trait approach to the study of geographic variation in the Amazonian frog Allobates femoralis : MULTI-TRAIT VARIATION IN AN AMAZONIAN FROG, 10.1111/j.1095-8312.2009.01324.x
  4. Andersson J., Borg-Karlson A.-K., Vongvanich N., Wiklund C., Male sex pheromone release and female mate choice in a butterfly, 10.1242/jeb.02726
  5. Arnegard Matthew E., McIntyre Peter B., Harmon Luke J., Zelditch Miriam L., Crampton William G. R., Davis Justin K., Sullivan John P., Lavoué Sébastien, Hopkins Carl D., Sexual Signal Evolution Outpaces Ecological Divergence during Electric Fish Species Radiation, 10.1086/655221
  6. Bacquet P. M. B., Brattstrom O., Wang H.- L., Allen C. E., Lofstedt C., Brakefield P. M., Nieberding C. M., Selection on male sex pheromone composition contributes to butterfly reproductive isolation, 10.1098/rspb.2014.2734
  7. Bandelt H. J., Forster P., Rohl A., Median-joining networks for inferring intraspecific phylogenies, 10.1093/oxfordjournals.molbev.a026036
  8. Bergen, Proc. R. Soc. Lond. B Biol. Sci., 6, 1758 (2013)
  9. Boul K. E, Chris Funk W, Darst C. R, Cannatella D. C, Ryan M. J, Sexual selection drives speciation in an Amazonian frog, 10.1098/rspb.2006.3736
  10. BRAKEFIELD PAUL M., REITSMA NICO, Phenotypic plasticity, seasonal climate and the population biology of Bicyclus butterflies (Satyridae) in Malawi, 10.1111/j.1365-2311.1991.tb00220.x
  11. Brakefield P. M., Beldade P., Zwaan B. J., The African Butterfly Bicyclus anynana: A Model for Evolutionary Genetics and Evolutionary Developmental Biology, 10.1101/pdb.emo122
  12. BUCKLEY STUART H., TREGENZA TOM, BUTLIN ROGER K., Transitions in cuticular composition across a hybrid zone: historical accident or environmental adaptation? : CUTICULAR COMPOSITION ACROSS A HYBRID ZONE, 10.1046/j.1095-8312.2003.00147.x
  13. Butlin Roger, Speciation by reinforcement, 10.1016/0169-5347(87)90193-5
  14. Clearwater J. R., Foster S. P., Muggleston S. J., Dugdale J. S., Priesner E., Intraspecific variation and interspecific differences in sex pheromones of sibling species inCtenopseustis obliquana complex, 10.1007/bf00994342
  15. Condamin, Monographie du genre Bicyclus (Lepidoptera: Satyridae) (1973)
  16. Darwin Charles, The descent of man, and selection in relation to sex /, 10.5962/bhl.title.110063
  17. Dopman Erik B., Robbins Paul S., Seaman Abby, COMPONENTS OF REPRODUCTIVE ISOLATION BETWEEN NORTH AMERICAN PHEROMONE STRAINS OF THE EUROPEAN CORN BORER : COMPONENTS OF REPRODUCTIVE ISOLATION, 10.1111/j.1558-5646.2009.00883.x
  18. Eltz Thomas, Zimmermann Yvonne, Pfeiffer Carolin, Pech Jorge Ramirez, Twele Robert, Francke Wittko, Quezada-Euan J. Javier G., Lunau Klaus, An Olfactory Shift Is Associated with Male Perfume Differentiation and Species Divergence in Orchid Bees, 10.1016/j.cub.2008.10.049
  19. Excoffier, Genetics, 131, 479 (1992)
  20. Excoffier Laurent, Laval Guillaume, Balding David, Gametic phase estimation over large genomic regions using an adaptive window approach, 10.1186/1479-7364-1-1-7
  21. Excoffier, Evol. Bioinfo. Online, 1, 47 (2005)
  22. Fay, Genetics, 155, 1405 (2000)
  23. Geiselhardt Sven, Otte Tobias, Hilker Monika, Looking for a similar partner: host plants shape mating preferences of herbivorous insects by altering their contact pheromones, 10.1111/j.1461-0248.2012.01816.x
  24. Grace Jaime L., Shaw Kerry L., Incipient sexual isolation inLaupala cerasina: Females discriminate population-level divergence in acoustic characters, 10.1093/czoolo/58.3.416
  25. Greenwood David R., Comeskey Dan, Hunt Martin B., Rasmussen L. Elizabeth L., Chemical communication: Chirality in elephant pheromones, 10.1038/4381097a
  26. Groot Astrid T., Inglis Olive, Bowdridge Scott, Santangelo Richard G., Blanco Carlos, López, Jr. Juan D., Vargas Antonio Terán, Gould Fred, Schal Coby, GEOGRAPHIC AND TEMPORAL VARIATION IN MOTH CHEMICAL COMMUNICATION, 10.1111/j.1558-5646.2009.00702.x
  27. Groot A. T., Staudacher H., Barthel A., Inglis O., Schöfl G., Santangelo R. G., Gebauer-Jung S., Vogel H., Emerson J., Schal C., Heckel D. G., Gould F., One quantitative trait locus for intra- and interspecific variation in a sex pheromone, 10.1111/mec.12171
  28. Heuskin Stéphanie, Vanderplanck Maryse, Bacquet Paul, Holveck Marie-Jeanne, Kaltenpoth Martin, Engl Tobias, Pels Christophe, Taverne Cédric, Lognay Georges, Nieberding Caroline M., The composition of cuticular compounds indicates body parts, sex and age in the model butterfly Bicyclus anynana (Lepidoptera), 10.3389/fevo.2014.00037
  29. Iyengar Vikram K., Rossini Carmen, Eisner Thomas, Precopulatory assessment of male quality in an arctiid moth (Utetheisa ornatrix): hydroxydanaidal is the only criterion of choice, 10.1007/s002650000292
  30. Johansson Björn G., Jones Therésa M., The role of chemical communication in mate choice, 10.1111/j.1469-185x.2007.00009.x
  31. de Jong MA, Kesbeke FMNH, Brakefield PM, Zwaan BJ, Geographic variation in thermal plasticity of life history and wing pattern in Bicyclus anynana, 10.3354/cr00881
  32. de Jong Maaike A., Wahlberg Niklas, van Eijk Marleen, Brakefield Paul M., Zwaan Bas J., Mitochondrial DNA Signature for Range-Wide Populations of Bicyclus anynana Suggests a Rapid Expansion from Recent Refugia, 10.1371/journal.pone.0021385
  33. Khannoon Eraqi R., Lunt David H., Schulz Stefan, Hardege Jörg D., Divergence of Scent Pheromones in Allopatric Populations ofAcanthodactylus boskianus(Squamata: Lacertidae), 10.2108/zsj.30.380
  34. Kikuyama Sakaé, Yamamoto Kazutoshi, Iwata Takeo, Toyoda Fumiyo, Peptide and protein pheromones in amphibians, 10.1016/s1096-4959(01)00534-6
  35. Klun J. A., Insect Sex Pheromones: Intraspecific Pheromonal Variability of Ostrinia nubilalis1 in North America and Europe2, 10.1093/ee/4.6.891
  36. LaForest Siana, Wu Wenqi, Löfstedt Christer, A Genetic Analysis of Population Differences in Pheromone Production and Response Between Two Populations of the Turnip Moth, Agrotis segetum, 10.1023/b:joec.0000006417.71996.46
  37. Landolt Peter J., Phillips Thomas W., HOST PLANT INFLUENCES ON SEX PHEROMONE BEHAVIOR OF PHYTOPHAGOUS INSECTS, 10.1146/annurev.ento.42.1.371
  38. Larsdotter-Mellström Helena, Murtazina Rushana, Borg-Karlson Anna-Karin, Wiklund Christer, Timing of Male Sex Pheromone Biosynthesis in a Butterfly – Different Dynamics under Direct or Diapause Development, 10.1007/s10886-012-0126-6
  39. Liénard Marjorie A, Wang Hong-Lei, Lassance Jean-Marc, Löfstedt Christer, Sex pheromone biosynthetic pathways are conserved between moths and the butterfly Bicyclus anynana, 10.1038/ncomms4957
  40. Linn C.E., Roelofs W.L., Response specificity of male moths to multicomponent pheromones, 10.1093/chemse/14.3.421
  41. L�fstedt Christer, Herrebout Wim M., Menken Steph B. J., Sex pheromones and their potential role in the evolution of reproductive isolation in small ermine moths (Yponomeutidae), 10.1007/bf01240662
  42. Martin J., Lopez P., Condition-Dependent Pheromone Signaling by Male Rock Lizards: More Oily Scents Are More Attractive, 10.1093/chemse/bjq009
  43. Masta S. E., Maddison W. P., Sexual selection driving diversification in jumping spiders, 10.1073/pnas.072493099
  44. McArdle Brian H., Anderson Marti J., FITTING MULTIVARIATE MODELS TO COMMUNITY DATA: A COMMENT ON DISTANCE-BASED REDUNDANCY ANALYSIS, 10.1890/0012-9658(2001)082[0290:fmmtcd]2.0.co;2
  45. Mendelson Tamra C., Shaw Kerry L., Sexual behaviour: Rapid speciation in an arthropod, 10.1038/433375a
  46. Monteiro Antónia, Pierce Naomi E, Phylogeny of Bicyclus (Lepidoptera: Nymphalidae) Inferred from COI, COII, and EF-1α Gene Sequences, 10.1006/mpev.2000.0872
  47. Nieberding Caroline M., de Vos Helene, Schneider Maria V., Lassance Jean-Marc, Estramil Natalia, Andersson Jimmy, Bång Joakim, Hedenström Erik, Löfstedt Christer, Brakefield Paul M., The Male Sex Pheromone of the Butterfly Bicyclus anynana: Towards an Evolutionary Analysis, 10.1371/journal.pone.0002751
  48. Nieberding Caroline M., Fischer Klaus, Saastamoinen Marjo, Allen Cerisse E., Wallin Erika A., Hedenström Erik, Brakefield Paul M., Cracking the olfactory code of a butterfly: the scent of ageing : The scent of ageing in a butterfly, 10.1111/j.1461-0248.2012.01748.x
  49. Oksanen, vegan: community ecology package (2011)
  50. Oneal E., Knowles L. L., Ecological selection as the cause and sexual differentiation as the consequence of species divergence?, 10.1098/rspb.2012.2236
  51. Palacio Cortés Angela M., Zarbin Paulo H.G., Takiya Daniela M., Bento J. Maurício S., Guidolin Aline S., Consoli Fernando L., Geographic variation of sex pheromone and mitochondrial DNA in Diatraea saccharalis (Fab., 1794) (Lepidoptera: Crambidae), 10.1016/j.jinsphys.2010.06.005
  52. Polzin Tobias, Daneshmand Siavash Vahdati, On Steiner trees and minimum spanning trees in hypergraphs, 10.1016/s0167-6377(02)00185-2
  53. Prudic K. L., Jeon C., Cao H., Monteiro A., Developmental Plasticity in Sexual Roles of Butterfly Species Drives Mutual Sexual Ornamentation, 10.1126/science.1197114
  54. Ritchie Michael G., Sexual Selection and Speciation, 10.1146/annurev.ecolsys.38.091206.095733
  55. Roelofs W. L., Du J. -W., Tang X. -H., Robbins P. S., Eckenrode C. J., Three European corn borer populations in New York based on sex pheromones and voltinism, 10.1007/bf01012071
  56. Roelofs W. L., Liu W., Hao G., Jiao H., Rooney A. P., Linn C. E., Evolution of moth sex pheromones via ancestral genes, 10.1073/pnas.152445399
  57. RUNEMARK A., GABIROT M., SVENSSON E. I., Population divergence in chemical signals and the potential for premating isolation between islet- and mainland populations of the Skyros wall lizard (Podarcis gaigeae) : Premating isolation and pheromones Podarcis lizards, 10.1111/j.1420-9101.2010.02214.x
  58. Ruther J., Matschke M., Garbe L.-A., Steiner S., Quantity matters: male sex pheromone signals mate quality in the parasitic wasp Nasonia vitripennis, 10.1098/rspb.2009.0738
  59. Safran Rebecca, Flaxman Samuel, Kopp Michael, Irwin Darren E., Briggs Derek, Evans Matthew R., Funk W. Chris, Gray David A., Hebets Eileen A., Seddon Nathalie, Scordato Elizabeth, Symes Laurel B., Tobias Joseph A., Toews David P. L., Uy J. Albert C., A robust new metric of phenotypic distance to estimate and compare multiple trait differences among populations, 10.1093/czoolo/58.3.426
  60. San Martin, Proc. Neth. Entomol. Soc. Meet., 22, 9 (2011)
  61. Sappington Thomas W., Taylor Orley R., Developmental and environmental sources of pheromone variation inColias eurytheme butterflies, 10.1007/bf00988085
  62. Sappington Thomas W., Taylor Orley R., Genetic sources of pheromone variation inColias eurytheme butterflies, 10.1007/bf00988084
  63. Schulz Stefan, Yildizhan Selma, van Loon Joop J. A., The Biosynthesis of Hexahydrofarnesylacetone in the Butterfly Pieris brassicae, 10.1007/s10886-011-9939-y
  64. Schwander Tanja, Arbuthnott Devin, Gries Regine, Gries Gerhard, Nosil Patrik, Crespi Bernard J, Hydrocarbon divergence and reproductive isolation in Timema stick insects, 10.1186/1471-2148-13-151
  65. Smadja C, Butlin R K, On the scent of speciation: the chemosensory system and its role in premating isolation, 10.1038/hdy.2008.55
  66. Sperling Felix, Byers Robert, Hickey Donal, Mitochondrial DNA sequence variation among pheromotypes of the dingy cutworm, Feltia jaculifera (Gn.) (Lepidoptera: Noctuidae), 10.1139/z96-240
  67. Steiger S., Schmitt T., Schaefer H. M., The origin and dynamic evolution of chemical information transfer, 10.1098/rspb.2010.2285
  68. SVENSSON GLENN P., WANG HONG-LEI, LASSANCE JEAN-MARC, ANDERBRANT OLLE, CHEN GUO-FA, GREGORSSON BERIT, GUERTIN CLAUDE, HARALA EEVAMARIA, JIRLE ERLING V., LIBLIKAS ILME, PETKO VLADIMIR, ROQUES ALAIN, ROSENBERG OLLE, STRONG WARD, VOOLMA KALJO, YLIOJA TIINA, WANG YAN-JUN, ZHOU XIAO-MING, LÖFSTEDT CHRISTER, Assessment of genetic and pheromonal diversity of theCydia strobilellaspecies complex (Lepidoptera: Tortricidae), 10.1111/j.1365-3113.2012.00662.x
  69. Tajima, Genetics, 123, 585 (1989)
  70. T�th Mikl�s, L�fstedt Christer, Blair Barry W., Cabello Tom�s, Farag Ali I., Hansson Bill S., Kovalev Boris G., Maini Stefano, Nesterov Evgeni A., Pajor Istv�n, Sazonov Aleksandr P., Shamshev Igor V., Subchev Mitko, Sz�cs G�bor, Attraction of male turnip mothsAgrotis segetum (Lepidoptera: Noctuidae) to sex pheromone components and their mixtures at 11 sites in Europe, Asia, and Africa, 10.1007/bf00994360
  71. Tregenza Tom, 10.1023/a:1021257114996
  72. Tregenza T., Pritchard V. L., Butlin R. K., PATTERNS OF TRAIT DIVERGENCE BETWEEN POPULATIONS OF THE MEADOW GRASSHOPPER, CHORTHIPPUS PARALLELUS, 10.1111/j.0014-3820.2000.tb00060.x
  73. Valtonen Anu, Molleman Freerk, Chapman Colin A., Carey James R., Ayres Matthew P., Roininen Heikki, Tropical phenology: bi-annual rhythms and interannual variation in an Afrotropical butterfly assemblage, 10.1890/es12-00338.1
  74. Wahlberg Niklas, Wheat Christopher West, Knowles L. Lacey, Genomic Outposts Serve the Phylogenomic Pioneers: Designing Novel Nuclear Markers for Genomic DNA Extractions of Lepidoptera, 10.1080/10635150802033006
  75. Wang Hong-Lei, Brattström Oskar, Brakefield Paul M., Francke Wittko, Löfstedt Christer, Identification and Biosynthesis of Novel Male Specific Esters in the Wings of the Tropical Butterfly, Bicyclus martius sanaos, 10.1007/s10886-014-0452-y
  76. Watts, Am. J. Trop. Med. Hyg., 73, 734 (2005)
  77. White Christopher S, Lambert David M, Genetic continuity within and discontinuities among, populations of leafroller moths with distinct sex-pheromones, 10.1038/hdy.1995.132
  78. WINDIG JACK J., BRAKEFIELD PAUL M., REITSMA NICO, WILSON JOHN G. M., Seasonal polyphenism in the wild: survey of wing patterns in five species of Bicyclus butterflies in Malawi, 10.1111/j.1365-2311.1994.tb00420.x
  79. Wyatt, Pheromones and animal behaviour: chemical signals and signatures (2014)
  80. Ballard J. William O., Whitlock Michael C., The incomplete natural history of mitochondria, 10.1046/j.1365-294x.2003.02063.x
  81. Bazin E., Population Size Does Not Influence Mitochondrial Genetic Diversity in Animals, 10.1126/science.1122033
  82. Bazinet , A. L. M. P. Cummings 2011 Computing the Tree of Life: leveraging the power of desktop and service grids IEEE Computer Society Washington, DC 1896 1902
  83. Brower A. V., Rapid morphological radiation and convergence among races of the butterfly Heliconius erato inferred from patterns of mitochondrial DNA evolution., 10.1073/pnas.91.14.6491
  84. Funk Daniel J., Omland Kevin E., Species-Level Paraphyly and Polyphyly: Frequency, Causes, and Consequences, with Insights from Animal Mitochondrial DNA, 10.1146/annurev.ecolsys.34.011802.132421
  85. Kergoat Gael J., Prowell Dorothy P., Le Ru Bruno P., Mitchell Andrew, Dumas Pascaline, Clamens Anne-Laure, Condamine Fabien L., Silvain Jean-François, Disentangling dispersal, vicariance and adaptive radiation patterns: A case study using armyworms in the pest genus Spodoptera (Lepidoptera: Noctuidae), 10.1016/j.ympev.2012.08.006
  86. Librado P., Rozas J., DnaSP v5: a software for comprehensive analysis of DNA polymorphism data, 10.1093/bioinformatics/btp187
  87. Munyuli M. B. Théodore, Butterfly Diversity from Farmlands of Central Uganda, 10.1155/2012/481509
  88. Paradis E., Claude J., Strimmer K., APE: Analyses of Phylogenetics and Evolution in R language, 10.1093/bioinformatics/btg412
  89. Posada D., jModelTest: Phylogenetic Model Averaging, 10.1093/molbev/msn083
  90. R Development Core Team, R: a language and environment for statistical computing (2011)
  91. Schliep Klaus Peter, phangorn: phylogenetic analysis in R, 10.1093/bioinformatics/btq706
  92. Shimodaira H., Hasegawa M., Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference, 10.1093/oxfordjournals.molbev.a026201
  93. Tamura K., Peterson D., Peterson N., Stecher G., Nei M., Kumar S., MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods, 10.1093/molbev/msr121
  94. Zwickl, Genetic algorithm approaches for the phylogenetic analysis of large biological sequence datasets under the maximum likelihood criterion (2006)