Rapid Divergent Evolution of Male Genitalia Among Populations of Drosophila buzzatii

Increasing evidence from multiple animal systems suggests that genital evolution and diversification are driven by rapid and strong evolutionary forces. Particularly, the morphology of male genital structures is considered to be among the fastest evolving traits in animal groups with internal fertil...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Soto, I.M
Otros Autores: Carreira, V.P, Soto, E.M, Márquez, F., Lipko, P., Hasson, E.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2013
Materias:
COI
Acceso en línea:Registro en Scopus
DOI
Handle
Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 19671caa a22014057a 4500
001 PAPER-11296
003 AR-BaUEN
005 20230518204126.0
008 190411s2013 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-84881369557 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
100 1 |a Soto, I.M. 
245 1 0 |a Rapid Divergent Evolution of Male Genitalia Among Populations of Drosophila buzzatii 
260 |c 2013 
270 1 0 |m Soto, I. M.; Departamento de Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón II, C1428 EHA Buenos Aires, Argentina; email: soto@ege.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Andrade, C.A.C., Hatadani, L.M., Klaczko, L.B., Phenotypic plasticity of the aedeagus of Drosophila mediopunctata (2005) Journal of Thermal Biology, 30, pp. 518-523 
504 |a Andrade, C.A.C., Vieira, R.D., Ananina, G., Klaczko, L.B., Evolution of the male genitalia: Morphological variation of the aedeagi in a natural population of Drosophila mediopunctata (2009) Genetica, 135 (1), pp. 13-23 
504 |a Arnqvist, G., The evolution of animal genitalia: Distinguishing between hypotheses by single species studies (1997) Biological Journal of the Linnean Society of London, 60, pp. 365-379 
504 |a Brommer, J.E., Wither PST? The approximation of QST by PST in evolutionary and conservation biology (2011) Journal of Evolutionary Biology, 24, pp. 1160-1168 
504 |a Cabrera, A.L., Regiones Fitogeográficas Argentinas (1976) Enciclopedia Argentina De Agricultura Y Jardinería, pp. 2-85. , W. F. Kugler (Ed.), Buenos Aires: Acme 
504 |a Cavalcanti, M.J., Mantel for Windows (2008) Test for association between two symmetric distance matrices with permutations iterations, , http://maurobio.infobio.net, Version 1. 19 
504 |a Coyne, J.A., Orr, H.A., (2004) Speciation, , Sunderland: Sinauer 
504 |a Crandall, K.A., Bininda-Emonds, O.R.P., Mace, G.M., Wayne, R.K., Considering evolutionary processes in conservation biology (2000) Trends in Ecology and Evolution, 15, pp. 290-295 
504 |a Crespi, B.J., The evolution of maladaptation (2000) Heredity, 84, pp. 623-629 
504 |a De Brito, R.A., Manfrin, M.H., Sene, F.M., Mitochondrial DNA phylogeography of Brazilian populations of Drosophila buzzatii (2002) Genetics and Molecular Biology, 25 (2), pp. 161-171 
504 |a Di Rienzo, J.A., Casanoves, F., Balzarini, M.G., Gonzalez, L., Tablada, M., Robledo, C.W., (2009) InfoStat ver. 2009, , http://www.infostat.com.ar/, InfoStat Group, FCA, Universidad Nacional de Córdoba, Argentina 
504 |a Dufour, L., Anatomie générale des Diptères (1844) Annuaire De Science Naturelle, 1, pp. 244-264 
504 |a Endler, J.A., (1977) Geographic Variation, Speciation, and Clines, , Princeton: Princeton University Press 
504 |a Fanara, J.J., Folguera, G., Iriarte, P.F., Mensch, J., Hasson, E., Genotype by environment interactions and development time in populations of cactophilic Drosophila (2006) Journal of Evolutionary Biology, 19, pp. 900-908 
504 |a Fernández Iriarte, P., Hasson, E., The role of the use of different host plants in the maintenance of the inversion polymorphism in the cactophilic Drosophila buzzatii (2000) Evolution, 54, pp. 1295-1302 
504 |a Fernández Iriarte, P., Rodríguez, C., Hasson, E., Inversion and allozyme polymorphism show contrasting patterns of microgeographic population structure in a natural population of Drosophila buzzatii (2002) Journal of Evolutionary Biology, 15, pp. 226-234 
504 |a Fontdevila, A., Ruiz, A., Ocaña, J., Alonso, G., The evolutionary history of Drosophila buzzatii. II. How much has chromosomal polymorphism changed in colonization? (1982) Evolution, 36, pp. 843-851 
504 |a Garnier, S., Magniez-Jannin, F., Rasplus, J.Y., Alibert, P., When morphometry meets genetics: Inferring the phylogeography of Carabus solieri using Fourier analyses of pronotum and male genitalia (2005) Journal of Evolutionary Biology, 18, pp. 269-280 
504 |a Gómez, G.A., Hasson, E., Transpecific polymorphisms in an inversion linked esterase locus in Drosophila buzzatii (2003) Molecular Biology and Evolution, 20, pp. 410-423 
504 |a Hasson, E., Fanara, J.J., Rodríguez, C., Vilardi, J.C., Reig, O.A., Fontdevila, A., The evolutionary history of Drosophila buzzatii. XXIV: Second chromosome inversions have different average effect on thorax length (1992) Heredity, 68, pp. 557-563 
504 |a Hasson, E., Rodríguez, C., Fanara, J.J., Naveira, H., Reig, A.O., Fontdevila, A., Macrogeographic patterns in the inversion polymorphisms of Drosophila buzzatii in New World populations (1995) Journal of Evolutionary Biology, 8, pp. 369-384 
504 |a Hasson, E., Soto, I.M., Carreira, V.P., Corio, C., Soto, E.M., Betti, M., Host plants, fitness and developmental instability in a guild of cactophilic species of the genus Drosophila (2009) Ecotoxicology Research Developments, pp. 89-109. , E. B. Santos (Ed.), Nueva York: Nova Science Publishers 
504 |a Hasson, E., Vilardi, J.C., Naveira, H., Fanara, J.J., Rodriguez, C., Reig, O.A., The evolutionary history of Drosophila buzzatii. XVI. Fitness components analysis in a natural original population from Argentina (1991) Journal of Evolutionary Biology, 4, pp. 209-225 
504 |a Hedrick, P.W., (2005) Genetics of Populations, , Boston: Jones and Bartlett 
504 |a Hendry, A.P., Taylor, E.B., McPhail, J.D., Adaptive divergence and the balance between selection and gene flow: Lake and stream stickleback in the Misty system (2002) Evolution, 56, pp. 1199-1216 
504 |a Hood, G.M., (2008) PopTools version 3. 0. 6, , http://www.cse.csiro.au/poptools, Available on the internet. URL 
504 |a Hosken, D.J., Stockley, P., Sexual selection and genital evolution (2004) Trends in Ecology and Evolution, 19, p. 8793 
504 |a House, C.M., Simmons, L.W., Genital morphology and fertilization success in the dung beetle Onthophagus taurus: An example of sexually selected male genitalia (2003) Proceedings of the Royal Society B, 270, pp. 447-455 
504 |a Iwata, H., Ukai, Y., SHAPE: A computer program package for quantitative evaluation of biological shapes based on Elliptic Fourier Descriptors (2002) Journal of Heredity, 93, pp. 384-385 
504 |a Jagadeeshan, S., Singh, R.S., A time-sequence functional analysis of mating behaviour and genital coupling in Drosophila: Role of cryptic female choice and male sex-drive in the evolution of male genitalia (2006) Journal of Evolutionary Biology, 19, pp. 1058-1070 
504 |a King, R.B., Lawson, R., Color-pattern variation in Lake Erie water snakes: The role of gene flow (1995) Evolution, 49, pp. 885-896 
504 |a Kopp, A., True, J.R., Evolution of male sexual characters in the Oriental Drosophila melanogaster species group (2002) Evolution and Development, 4, pp. 278-291 
504 |a Kuhl, F.P., Giardina, C.R., Elliptic Fourier features of a closed contour (1982) Computer Graphics and Image Processing, 18, pp. 236-258 
504 |a Laayouni, H., Hasson, E., Santos, M., Fontdevila, A., The evolutionary history of Drosophila buzzatii. XXXV. Inversion polymorphism and nucleotide variability in different regions of the second chromosome (2003) Molecular Biology and Evolution, 20, pp. 931-944 
504 |a Leinonen, T., O'Hara, R., Cano, J.M., Merilä, J., Comparative studies of quantitative trait and neutral marker divergence: A meta-analysis (2008) Journal of Evolutionary Biology, 21, pp. 1-17 
504 |a Lenormand, T., Gene flow and the limits to natural selection (2002) Trends in Ecology and Evolution, 17, pp. 183-189 
504 |a Lu, G., Bernatchez, L., Correlated trophic specialization and genetic divergence in sympatric lake whitefish ecotypes (Coregonus clupeaformis): Support for the ecological speciation hypothesis (1999) Evolution, 53, pp. 1491-1505 
504 |a Manfrin, M.H., Sene, F.M., Cactophilic Drosophila in South America: A model for evolutionary studies (2006) Genetica, 126, pp. 57-75 
504 |a Markow, T.A., O'Grady, P.M., (2006) Drosophila: A Guide for Species Identification and Use, , London: Academic Press 
504 |a Masly, J.P., 170 years of "lock-and-key": Genital morphology and reproductive isolation (2012) International Journal of Evolutionary Biology, , doi:10.1155/2012/247352 
504 |a McPeek, M.A., Shen, L., Torrey, J.Z., Farid, H., The tempo and mode of three-dimensional morphological evolution in male reproductive structures (2008) American Naturalist, 171, pp. 158-178 
504 |a Nei, M., Genetic distance between populations (1972) American Naturalist, 106, pp. 283-292 
504 |a Piccinali, R., Aguadé, M., Hasson, E., Comparative molecular population genetics of the Xdh locus in the cactophilic sibling species Drosophila buzzatii and D. koepferae (2004) Molecular Biology and Evolution, 21, pp. 141-152 
504 |a Piccinali, R.V., Mascord, L.J., Barker, J.S., Oakeshott, J.G., Hasson, E., Molecular population genetics of the alpha-esterase5 gene locus in original and colonized populations of Drosophila buzzatii and its sibling Drosophila koepferae (2007) Journal of Molecular Evolution, 64, pp. 158-170 
504 |a Polihronakis Richmond, M., Johnson, S., Markow, T.A., Evolution of reproductive morphology among recently diverged taxa in the Drosophila mojavensis species cluster (2012) Ecology and Evolution, 2 (2), pp. 397-408 
504 |a Pomiankowski, A., Möller, A.P., A resolution of the lek paradox (1995) Proceedings of the Royal Society B, 260, pp. 21-29 
504 |a Pujol, B., Wilson, A.J., Ross, R.I.C., Pannell, J.R., Are Q(ST)-F-ST comparisons for natural populations meaningful? (2008) Molecular Ecology, 17, pp. 4782-4785 
504 |a Raeymaekers, J.A.M., van Houdt, J.K.J., Larmuseau, M.H.D., Geldof, S., Volckaert, F.A.M., Divergent selection as revealed by PST and QTL-based FST in three-spined stickle- back (Gasterosteus aculeatus) populations along a coastal-inland gradient (2007) Molecular Ecology, 16, pp. 891-905 
504 |a Riechert, S.E., Singer, F.D., Jones, T.C., High gene flow levels lead to gamete wastage in a desert spider system (2001) Genetica, 112, pp. 297-319 
504 |a Rodríguez, C., Piccinali, R., Levy, E., Hasson, E., Contrasting population genetic structures using allozymes and the inversion polymorphism in Drosophila buzzatii (2000) Journal of Evolutionary Biology, 13, pp. 976-984 
504 |a Rohlf, F.J., Archie, J.W., A comparison of Fourier methods for the description of wing shape in mosquitoes (Diptera: Culicidae) (1984) Systematic Biology, 33, pp. 302-317 
504 |a Ross, K.G., Keller, L., Joint influence of gene flow and selection on a reproductively important genetic polymorphism in the fire ant Solenopsis invicta (1995) American Naturalist, 146, pp. 325-348 
504 |a Rossi, M.S., Barrio, E., Latorre, A., Quezada-Díaz, J.E., Hasson, E., Moya, A., The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations (1996) Molecular Biology and Evolution, 13, pp. 314-323 
504 |a Saint-Laurent, R., Legault, M., Bernatchez, L., Divergent selection maintains adaptive differentiation despite high gene flow between sympatric rainbow smelt ecotypes (2003) Molecular Ecology, 12, pp. 315-330 
504 |a Sandoval, C.P., The effects of relative geographic scales of gene flow and selection on morph frequencies in the walking stick Timema cristinae (1994) Evolution, 48, pp. 1866-1879 
504 |a Schluter, D., Ecological causes of speciation (1998) Endless Forms: Species and Speciation, pp. 114-129. , D. J. Howard and S. H. Berlocher (Eds.), Oxford: Oxford University Press 
504 |a Schluter, D., (2000) The Ecology of Adaptive Radiation, , Oxford: Oxford University Press 
504 |a Slatkin, M., Gene flow and the geographic structure of natural populations (1987) Science, 236, pp. 787-792 
504 |a Smith, T.B., Wayne, R.K., Girman, D.J., Bruford, M.W., A role for ecotones in generating rainforest biodiversity (1997) Science, 276, pp. 1855-1857 
504 |a Soto, I.M., Aedeagal divergence in sympatric populations of two sibling species of cactophilic Drosophila (Diptera, Drosophilidae): Evidence of character displacement? (2012) Neotropical Entomology, 41 (3), pp. 207-213 
504 |a Soto, I.M., Carreira, V.P., Fanara, J.J., Hasson, E., Evolution of male genitalia: Environmental and genetic factors affecting genital morphology in sibling Drosophila species and their hybrids (2007) BMC Evolutionary Biology, 7, p. 77 
504 |a Soto, I.M., Manfrin, M.H., Hasson, E., Host-dependent phenotypic plasticity of male genital morphology in cactophilic Drosophila (2008) Journal of Zoological Systematics and Evolutionary Research, 46, pp. 368-373 
504 |a Soto, I.M., Soto, E.M., Carreira, V.P., Hurtado, J., Fanara, J.J., Hasson, E., Geographic patterns of inversion polymorphism in the second chromosome of the cactophilic Drosophila buzzatii from northeastern Argentina (2010) Journal of Insect Science, 10, p. 181 
504 |a Spitze, K., Population structure in Daphnia obtusa: Quantitative genetic and allozyme variation (1993) Genetics, 135, pp. 367-374 
504 |a (2001) STATISTICA (data analysis software system), version 6. 0, , www.statsoft.com, StatSoft Inc 
504 |a Storfer, A., Cross, J., Rush, R., Caruso, J., Adaptive coloration and gene flow as a constraint to local adaptation in the streamside salamander, Ambystoma barbouri (1999) Evolution, 53, pp. 889-898 
504 |a 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 (2011) Molecular Biology and Evolution, 28 (10), pp. 2731-2739 
504 |a Tazzyman, S.J., Iwasa, Y., Sexual selection can increase the effect of random genetic drift-Quantitative genetic model of polymorphism in Oophaga pumilio, the strawberry poison-dart frog (2010) Evolution, 64, pp. 1558-5646 
504 |a Uyeda, J.C., Arnold, S.J., Hohenlohe, P.A., Mead, L.S., Drift promotes speciation by sexual selection (2009) Evolution, 63, pp. 583-594 
504 |a Valdano, S.G., Di Rienzo, J., Discovering meaningful groups in hierarchical cluster analysis (2007) An extension to the multivariate case of a multiple comparison method based on cluster analysis, , http://interstat.statjournals.net/YEAR/2007/abstracts/0704002.php, InterStat 
504 |a Vilela, C.R., A revision of the Drosophila repleta species group (Diptera, Drosophilidae) (1983) Revista Brasilera De Entomología, 27, pp. 1-114 
504 |a Vilela, C.R., Brito da Cunha, A., On marta breuer and some of her unpublished drawings of Drosophila spp. male terminalia (Diptera, Drosophilidae) (2006) Genetics and Molecular Biology, 587, pp. 580-587 
504 |a Whitlock, M.C., Evolutionary inference from Qst (2008) Molecular Ecology, 17, pp. 1885-1896 
504 |a Wojcieszek, J.M., Simmons, L.W., Evidence for stabilizing selection and slow divergent evolution of males genitalia in a millipede (Antichiropus variabilis) (2012) Evolution, 66 (4), pp. 1138-1153 
520 3 |a Increasing evidence from multiple animal systems suggests that genital evolution and diversification are driven by rapid and strong evolutionary forces. Particularly, the morphology of male genital structures is considered to be among the fastest evolving traits in animal groups with internal fertilization. In this study, we investigated patterns of male genital variation within and between natural populations of the cactophilic fly Drosophila buzzatii in its original geographic distribution range in the Neotropics. We detected significant morphological differences among populations and distinguished five differentiated groups. Moreover, among population differentiation in genital morphology was associated with the degree of geographic isolation among populations and clearly contrasted with the general homogeneity detected for the putatively neutral mitochondrial gene COI. Integrating our present data with previous molecular population genetic surveys, our results suggest that male genital morphology has rapidly diverged after the recent demographic expansion that D. buzzatii has undergone in the arid zones of South America. Because the "lock and key" hypothesis failed to explain the present pattern, we explored alternative explanations for the observed pattern of genital diversification including drift-facilitated sexual selection. © 2013 Springer Science+Business Media New York.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Acknowledgments The authors wish to thank F. F. Franco and M. Polihronakis Richmond for helpful discussions in early stages of this investigation and in the drafting of the manuscript respectively. We are also grateful to two anonymous reviewers whose insightful advice and corrections helped to greatly improve the original manuscript. This work was supported by grants of Universidad de Buenos Aires, ANPCyT and CONICET. P. L., F. M. and E. M. S. are recipients of postgraduate and postdoctoral scholarships of CONICET respectively. I. M. S., V. P. C. and E. H. are members of Carrera del Investigador Científico (CONICET). 
593 |a Departamento de Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón II, C1428 EHA Buenos Aires, Argentina 
593 |a Biología y Manejo de Recursos Acuáticos, Centro Nacional Patagónico, Consejo Nacional de Investigaciones Científicas y Técnicas, Blvd. Brown 2915, U9120ACF Puerto Madryn, Chubut, Argentina 
593 |a Universidad Nacional de la Patagonia San Juan Bosco, Blvd Brown 3100, U9120ACF Puerto Madryn, Chubut, Argentina 
593 |a Instituto de Ecología, Genética y Evolución de Buenos Aires (IEGEBA)-CONICET, Buenos Aires, Argentina 
690 1 0 |a AEDEAGUS 
690 1 0 |a CHROMOSOMAL INVERSION 
690 1 0 |a DRIFT 
690 1 0 |a MORPHOLOGICAL EVOLUTION 
690 1 0 |a PST 
690 1 0 |a ANIMALIA 
690 1 0 |a DROSOPHILA BUZZATII 
650 1 7 |2 spines  |a COI 
700 1 |a Carreira, V.P. 
700 1 |a Soto, E.M. 
700 1 |a Márquez, F. 
700 1 |a Lipko, P. 
700 1 |a Hasson, E. 
773 0 |d 2013  |g v. 40  |h pp. 395-407  |k n. 3  |p Evol. Biol.  |x 00713260  |w (AR-BaUEN)CENRE-4024  |t Evolutionary Biology 
856 4 1 |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-84881369557&doi=10.1007%2fs11692-013-9223-x&partnerID=40&md5=6ac00df79248cf715696b55b70396af7  |y Registro en Scopus 
856 4 0 |u https://doi.org/10.1007/s11692-013-9223-x  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00713260_v40_n3_p395_Soto  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00713260_v40_n3_p395_Soto  |y Registro en la Biblioteca Digital 
961 |a paper_00713260_v40_n3_p395_Soto  |b paper  |c PE 
962 |a info:eu-repo/semantics/article  |a info:ar-repo/semantics/artículo  |b info:eu-repo/semantics/publishedVersion 
999 |c 72249