The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Genomic linkage of male song and female acoustic preference QTL underlying a rapid species radiation
Open accessAbstract
The genetic coupling hypothesis of signal-preference evolution, whereby the same genes control male signal and female preference for that signal, was first inspired by the evolution of cricket acoustic communication nearly 50 years ago. To examine this hypothesis, we compared the genomic location of quantitative trait loci (QTL) underlying male song and female acoustic preference variation in the Hawaiian cricket genus Laupala . We document a QTL underlying female acoustic preference variation between 2 closely related species ( Laupala kohalensis and Laupala paranigra ). This preference QTL colocalizes with a song QTL identified previously, providing compelling evidence for a genomic linkage of the genes underlying these traits. We show that both song and preference QTL make small to moderate contributions to the behavioral difference between species, suggesting that divergence in mating behavior among Laupala species is due to the fixation of many genes of minor effect. The diversity of acoustic signaling systems in crickets exemplifies the evolution of elaborate male displays by sexual selection through female choice. Our data reveal genetic conditions that would enable functional coordination between song and acoustic preference divergence during speciation, resulting in a behaviorally coupled mode of signal-preference evolution. Interestingly, Laupala exhibits one of the fastest rates of speciation in animals, concomitant with equally rapid evolution in sexual signaling behaviors. Genomic linkage may facilitate rapid speciation by contributing to genetic correlations between sexual signaling behaviors that eventually cause sexual isolation between diverging populations.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In Hawaiian crickets, male song traits and female preferences are physically linked in the genome, a coupling that may speed up sexual selection and even speciation”
From Listening forward: emerging roles of bioacoustics in ecology, evolution, and conservation (2026) · cites this paper as Shaw and Lesnick 2009
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
AFLP: a new technique for DNA fingerprinting
Vos, P., Hogers, R. C. J., Bleeker, M., Reijans, M., van de Lee, T., Hornes, M., Frijters, A., Pot, J., Paleman, J., Kuiper, M. T. R., et al. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.21.4407 · Cited by 12,405
Sexual Selection and the Descent of Man
(2017) · Routledge eBooks · doi:10.4324/9781315129266 · Cited by 7,287
Empirical threshold values for quantitative trait mapping.
Churchill, G. A., & Doerge, R. W. (1994) · Genetics · doi:10.1093/genetics/138.3.963 · Cited by 4,935
R/qtl: QTL mapping in experimental crosses
Broman, K. W., Wu, H., Sen, Ś., & Churchill, G. A. (2003) · Bioinformatics · doi:10.1093/bioinformatics/btg112 · Cited by 3,481
Sexual selection and mate choice
Andersson, M., & Simmons, L. W. (2006) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2006.03.015 · Cited by 1,269
Sexual selection and speciation
Panhuis, T. M., Butlin, R. K., Zuk, M., & Tregenza, T. (2001) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(01)02160-7 · Cited by 898
Simmons, A. M., Popper, A. N., & Fay, R. R. (2003) · Springer eBooks · doi:10.1007/b98903 · Cited by 767
Sexual Selection and Speciation
Ritchie, M. G. (2007) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev.ecolsys.38.091206.095733 · Cited by 731
Acoustic Communication in Insects and Anurans: Common Problems and Diverse Solutions
Gerhardt, H. C., Huber, F., & Simmons, A. M. (2003) · The Journal of the Acoustical Society of America · doi:10.1121/1.1591773 · Cited by 683
Acoustic communication in insects and anurans: Common problems and diverse solutions
(2003) · Computers & Mathematics with Applications · doi:10.1016/s0898-1221(03)90067-8 · Cited by 680
Research works printed but not linked: 1
- D Otte The Crickets of Hawaii: Origin, Systematics and Evolution (The Orthopterists' Society, Acad of Nat Sci of Philadelphia, Philadelphia, 1994).
Cited by
Sorted by citations
Genomics and the origin of species
D, O. S. C., Butlin, R. K., Keller, I., Wagner, C. E., BOUGHMAN, J. W., Hohenlohe, P. A., Peichel, C. L., Sætre, G., Bank, C., Brännström, Å., et al. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3644 · Cited by 1,045
Evolutionary divergence in acoustic signals: causes and consequences
Wilkins, M. R., Nathalie Seddon, A., & Safran, R. J. (2012) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2012.10.002 · Cited by 507
The genes underlying the process of speciation
Nosil, P., & Schluter, D. (2011) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2011.01.001 · Cited by 346
Kopp, M., Servedio, M. R., Mendelson, T. C., Safran, R. J., Rodrı́guez, R. L., Hauber, M. E., Scordato, E. S. C., Symes, L. B., Balakrishnan, C. N., Zonana, D. M., et al. (2017) · The American Naturalist · doi:10.1086/694889 · Cited by 205
An auditory feature detection circuit for sound pattern recognition
Schöneich, S., Kostarakos, K., & Hedwig, B. (2015) · Science Advances · doi:10.1126/sciadv.1500325 · Cited by 121
Pervasive genetic associations between traits causing reproductive isolation inHeliconiusbutterflies
Merrill, R. M., Schooten, B. V., Scott, J. A., & Jiggins, C. D. (2010) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2010.1493 · Cited by 111
Bengston, S. E., Dahan, R. A., Donaldson, Z. R., Phelps, S. M., van Oers, K., Sih, A., & Bell, A. M. (2018) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0411-4 · Cited by 120
Smadja, C. M., Canbäck, B., Vitalis, R., Gautier, M., Ferrari, J., Zhou, J., & Butlin, R. K. (2012) · Evolution · doi:10.1111/j.1558-5646.2012.01612.x · Cited by 116
Bousquet, F., Nojima, T., Houot, B., Chauvel, I., Chaudy, S., Dupas, S., Yamamoto, D., & Ferveur, J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109166108 · Cited by 107
Insights into the genomic evolution of insects from cricket genomes
Ylla, G., Nakamura, T., Itoh, T., Kajitani, R., Toyoda, A., Tomonari, S., Bando, T., Ishimaru, Y., Watanabe, T., Fuketa, M., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02197-9 · Cited by 101
The Genetic Basis of Sexually Selected Variation
Chenoweth, S. F., & McGuigan, K. (2010) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev-ecolsys-102209-144657 · Cited by 95
Transcriptomics of morphological color change in polychromatic Midas cichlids
Henning, F., Jones, J. C., Franchini, P., & Meyer, A. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-171 · Cited by 95
Genetic dissection of assortative mating behavior
Merrill, R. M., Rastas, P. M. A., Martin, S. H., Melo, M. C., Barker, S. L., Davey, J. W., McMillan, W. O., & Jiggins, C. D. (2019) · PLoS Biology · doi:10.1371/journal.pbio.2005902 · Cited by 92
The draft genome of a socially polymorphic halictid bee, Lasioglossum albipes
Kocher, S. D., Li, C., Yang, W. C., Tan, H., Yi, S. V., Yang, X., Hoekstra, H. E., Zhang, G., Pierce, N. E., & Yu, D. W. (2013) · Genome biology · doi:10.1186/gb-2013-14-12-r142 · Cited by 84
Gould, F. L., Estock, M. L., Hillier, N. K., Powell, B., Groot, A. T., Ward, C. M., Emerson, J. L., Schal, C., & Vickers, N. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910945107 · Cited by 82
Genes versus phenotypes in the study of speciation
Shaw, K. L., & Mullen, S. P. (2011) · Genetica · doi:10.1007/s10709-011-9562-4 · Cited by 76
Self-citationEvolution of Acoustic Communication in Insects
Greenfield, M. D. (2016) · Springer handbook of auditory research · doi:10.1007/978-3-319-28890-1_2 · Cited by 74
Bay, R. A., Arnegard, M. E., Conte, G. L., Best, J., Bedford, N. L., McCann, S. R., Dubin, M., Chan, Y. F., Jones, F. C., Kingsley, D. M., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.09.037 · Cited by 73
Speciation by sexual selection: 20 years of progress
Mendelson, T. C., & Safran, R. J. (2021) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2021.09.004 · Cited by 70
Purring Crickets: The Evolution of a Novel Sexual Signal
Tinghitella, R. M., Broder, E. D., Gurule‐Small, G. A., Hallagan, C. J., & Wilson, J. D. (2018) · The American Naturalist · doi:10.1086/700116 · Cited by 70
Grace, J. L., & Shaw, K. L. (2011) · Evolution · doi:10.1111/j.1558-5646.2011.01278.x · Cited by 69
Self-citationWidespread genetic linkage of mating signals and preferences in the Hawaiian cricket Laupala
Wiley, C., Ellison, C. K., & Shaw, K. L. (2011) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2011.1740 · Cited by 68
Self-citationDual control by a single gene of secondary sexual characters and mating preferences in medaka
Fukamachi, S., Kinoshita, M., Aizawa, K., Oda, S., Meyer, A., & Mitani, H. (2009) · BMC Biology · doi:10.1186/1741-7007-7-64 · Cited by 68
Salvemini, M., Polito, C., & Saccone, G. (2010) · Journal of Genetics · doi:10.1007/s12041-010-0040-z · Cited by 58
Insect Speciation Rules: Unifying Concepts in Speciation Research
Mullen, S. P., & Shaw, K. L. (2011) · Annual Review of Entomology · doi:10.1146/annurev-ento-120710-100621 · Cited by 56
Self-citationIndividual mating decisions and hybridization
Rosenthal, G. G. (2013) · Journal of Evolutionary Biology · doi:10.1111/jeb.12004 · Cited by 55
Brand, P., Hinojosa-Díaz, I. A., Ayala, R., Daigle, M., Yurrita, C. L., Eltz, T., & Ramírez, S. R. (2020) · Nature Communications · doi:10.1038/s41467-019-14162-6 · Cited by 56
Zeng, V., Ewen‐Campen, B., Horch, H. W., Roth, S., Mito, T., & Extavour, C. G. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061479 · Cited by 51
Ellison, C. K., WILEY, C., & Shaw, K. L. (2011) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2011.02244.x · Cited by 50
Self-citationGenomic signatures accompanying the dietary shift to phytophagy in polyphagan beetles
Seppey, M., Ioannidis, P., Emerson, B. C., Pitteloud, C., Robinson‐Rechavi, M., Roux, J., Escalona, H. E., McKenna, D. D., Misof, B. Y., Shin, S., et al. (2019) · Genome biology · doi:10.1186/s13059-019-1704-5 · Cited by 50
Genetic coupling of signal and preference facilitates sexual isolation during rapid speciation
Xu, M., & Shaw, K. L. (2019) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2019.1607 · Cited by 48
Self-citationHenry, C. S., & Wells, M. L. M. (2010) · Animal Behaviour · doi:10.1016/j.anbehav.2010.08.021 · Cited by 45
Ronacher, B. (2019) · Journal of Comparative Physiology A · doi:10.1007/s00359-018-01311-3 · Cited by 44
Xu, M., & Shaw, K. L. (2021) · Journal of Heredity · doi:10.1093/jhered/esab001 · Cited by 44
Self-citationCande, J., Andolfatto, P., Prud’homme, B., Stern, D. L., & Gompel, N. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043888 · Cited by 41
Wiley, C., & Shaw, K. L. (2010) · Evolution · doi:10.1111/j.1558-5646.2010.01007.x · Cited by 40
Self-citationBlankers, T., Oh, K. P., Bombarely, A., & Shaw, K. L. (2018) · Genetics · doi:10.1534/genetics.118.300894 · Cited by 39
Self-citationParallel changes in mate-attracting calls and female preferences in autotriploid tree frogs
Tucker, M. A., & Gerhardt, H. C. (2011) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2011.1968 · Cited by 38
Sweigart, A. L. (2009) · Genetics · doi:10.1534/genetics.109.111245 · Cited by 38
A framework for studying behavioral evolution by reconstructing ancestral repertoires
Hernández, D. G., Rivera, C., Cande, J., Zhou, B., Stern, D. L., & Berman, G. J. (2021) · eLife · doi:10.7554/elife.61806 · Cited by 44
QTL for the species‐specific male and female genital morphologies in Ohomopterus ground beetles
Sasabe, M., Takami, Y., & Sota, T. (2010) · Molecular Ecology · doi:10.1111/j.1365-294x.2010.04883.x · Cited by 37
The hypothesis of adaptive radiation in evolutionary biology: hard facts about a hazy concept
Soulebeau, A., Aubriot, X., Gaudeul, M., Rouhan, G., Hennequin, S., Haevermans, T., Dubuisson, J., & Jabbour, F. (2015) · Organisms Diversity & Evolution · doi:10.1007/s13127-015-0220-z · Cited by 36
Blankers, T., Oh, K. P., & Shaw, K. L. (2019) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2019.1479 · Cited by 34
Self-citationPleiotropy, “sexy” traits, and speciation
Shaw, K. L., Ellison, C. K., Oh, K. P., & Wiley, C. (2011) · Behavioral Ecology · doi:10.1093/beheco/arr136 · Cited by 34
Self-citationHouot, B., Bousquet, F., & Ferveur, J. (2010) · Genetics · doi:10.1534/genetics.110.117226 · Cited by 32
Oh, K. P., Fergus, D. J., Grace, J. L., & Shaw, K. L. (2012) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2012.02531.x · Cited by 33
Self-citationEvolutionary novelty in communication between the sexes
Broder, E. D., Elias, D. O., Rodrı́guez, R. L., Rosenthal, G. G., Seymoure, B., & Tinghitella, R. M. (2021) · Biology Letters · doi:10.1098/rsbl.2020.0733 · Cited by 31
Grace, J. L., & Shaw, K. L. (2012) · Current Zoology · doi:10.1093/czoolo/58.3.416 · Cited by 31
Self-citationGenetic basis of male colour dimorphism in a L ake T anganyika cichlid fish
Takahashi, T., Sota, T., & Hori, M. (2012) · Molecular Ecology · doi:10.1111/mec.12120 · Cited by 29
Genetic basis of species-specific genitalia reveals role in species diversification
Fujisawa, T., Sasabe, M., Nagata, N., Takami, Y., & Sota, T. (2019) · Science Advances · doi:10.1126/sciadv.aav9939 · Cited by 30
Bellamy, L., Chapman, N. C., Fowler, K., & Pomiankowski, A. (2013) · Evolution · doi:10.1111/evo.12135 · Cited by 28
The causes of variation in the presence of genetic covariance between sexual traits and preferences
Fowler‐Finn, K. D., & Rodrı́guez, R. L. (2015) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12182 · Cited by 25
Satellite DNAs are conserved and differentially transcribed among Gryllus cricket species
Palacios-Gimenez, O. M., Bardella, V. B., Lemos, B., & Cabral-de-Mello, D. C. (2017) · DNA Research · doi:10.1093/dnares/dsx044 · Cited by 24
IDENTIFICATION OF GENETICALLY LINKED FEMALE PREFERENCE AND MALE TRAIT
McNiven, V. T. K., & Moehring, A. J. (2013) · Evolution · doi:10.1111/evo.12096 · Cited by 24
Bailey, R. I., Tesaker, M. R., Trier, C. N., & Sætre, G. (2015) · Journal of Evolutionary Biology · doi:10.1111/jeb.12652 · Cited by 24
Jacob, P. F., & Hedwig, B. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.04.025 · Cited by 24
van der Sluijs, I., D, O. S. C., Dooren, T. J. M. V., & van Alphen, J. J. M. (2010) · Current Zoology · doi:10.1093/czoolo/56.1.57 · Cited by 23
Lemmon, E. M., & Juenger, T. (2017) · Ecology and Evolution · doi:10.1002/ece3.3443 · Cited by 22
Ecology and the Origin of Nonephemeral Species
Anderson, S. A. S., López‐Fernández, H., & Weir, J. T. (2022) · The American Naturalist · doi:10.1086/723763 · Cited by 23
Diet alters Drosophila melanogaster mate preference and attractiveness
Schultzhaus, J. N., Nixon, J. J., Duran, J. A., & Carney, G. E. (2016) · Animal Behaviour · doi:10.1016/j.anbehav.2016.11.012 · Cited by 21
anyFish: an open-source software to generate animated fish models for behavioural studies
Veen, T., Ingley, S. J., Cui, R., Simpson, J., Asl, M. R., Zhang, J., Butkowski, T., Wen, L., Hash, C., Johnson, J. B., et al. (2013) · Padua Research Archive (University of Padova) · Cited by 21
Coevolution of cognitive abilities and identity signals in individual recognition systems
Miller, S., Sheehan, M. J., & Reeve, H. K. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0467 · Cited by 21
Ding, B., Daugherty, D. W., Husemann, M., Chen, M., Howe, A. E., & Danley, P. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0114798 · Cited by 21
Ingley, S. J., Asl, M. R., Wu, C., Cui, R., Gadelhak, M., Li, W., Zhang, J., Simpson, J., Hash, C., Butkowski, T., et al. (2015) · SoftwareX · doi:10.1016/j.softx.2015.10.001 · Cited by 21
Ratterman, N. L., Rosenthal, G. G., Carney, G. E., & Jones, A. G. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.007468 · Cited by 17
Martin, C. H., McGirr, J. A., Richards, E. J., & John, M. E. S. (2019) · Integrative Organismal Biology · doi:10.1093/iob/obz018 · Cited by 17
Nakamura, T., Ylla, G., & Extavour, C. G. M. (2022) · Current Opinion in Insect Science · doi:10.1016/j.cois.2022.100881 · Cited by 17
Evolution of Call Patterns and Pattern Recognition Mechanisms in Neoconocephalus Katydids
Schul, J., Bush, S. L., & Frederick, K. (2013) · Animal signals and communication · doi:10.1007/978-3-642-40462-7_10 · Cited by 17
The Genetics of a Behavioral Speciation Phenotype in an Island System
Blankers, T., Oh, K. P., & Shaw, K. L. (2018) · Genes · doi:10.3390/genes9070346 · Cited by 16
Self-citationSteiger, S., Capodeanu-Nägler, A., Gershman, S. N., Weddle, C. B., Rapkin, J., Sakaluk, S. K., & Hunt, J. (2015) · Journal of Evolutionary Biology · doi:10.1111/jeb.12740 · Cited by 16
Oppenheim, S. J., Gould, F. L., & Hopper, K. R. (2012) · Evolution · doi:10.1111/j.1558-5646.2012.01712.x · Cited by 14
Rapid sexual signal diversification is facilitated by permissive females
Zhang, R., Rayner, J. G., & Bailey, N. W. (2023) · Current Biology · doi:10.1016/j.cub.2023.11.063 · Cited by 14
Chemical Communication: A Jewel Sheds Light on Signal Evolution
Lassance, J., & Löfstedt, C. (2013) · Current Biology · doi:10.1016/j.cub.2013.03.055 · Cited by 14
On the logic of Fisherian sexual selection*
Veller, C., Muralidhar, P., & Haig, D. (2020) · Evolution · doi:10.1111/evo.13944 · Cited by 14
COMMUNITY COMPOSITION AFFECTS THE SHAPE OF MATE RESPONSE FUNCTIONS
Symes, L. B. (2014) · Evolution · doi:10.1111/evo.12415 · Cited by 14
Variation in Melanism and Female Preference in Proximate but Ecologically Distinct Environments
Culumber, Z. W., Bautista-Hernández, C. E., Monks, S., Arias‐Rodríguez, L., & Tobler, M. (2014) · Ethology · doi:10.1111/eth.12282 · Cited by 13
Auditory DUM neurons in a bush‐cricket: A filter bank for carrier frequency
Lefebvre, P. C., Seifert, M., & Stumpner, A. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24399 · Cited by 13
Blankers, T., Lübke, A. K., & Hennig, R. M. (2015) · Journal of Evolutionary Biology · doi:10.1111/jeb.12686 · Cited by 13
A pleiotropic chemoreceptor facilitates the production and perception of mating pheromones
Vernier, C., Leitner, N. E., Zelle, K. M., Foltz, M., Dutton, S., Liang, X., Halloran, S. T., Millar, J. G., & Ben‐Shahar, Y. (2022) · iScience · doi:10.1016/j.isci.2022.105882 · Cited by 12
Within-population variability in a moth sex pheromone blend, part 2: selection towards fixation
Groot, A. T., van Wijk, M., Perez, E. V., Kuperus, P., Schöfl, G., Veldhuizen, D. V., & Heckel, D. G. (2019) · Royal Society Open Science · doi:10.1098/rsos.182050 · Cited by 12
Genetic Coupling of Mate Recognition Systems in the Genomic EraPreprint
Ritchie, M. G., & Butlin, R. K. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041437 · Cited by 12
Wolbachia infection in the Loxoblemmus complex (Orthoptera: Gryllidae) in Korea
Jeong, G., Ahn, J., Jang, Y., Choe, J. C., & Choi, H. (2012) · Journal of Asia-Pacific Entomology · doi:10.1016/j.aspen.2012.07.002 · Cited by 11
Perry, J. C., & Mank, J. E. (2014) · Wiley eBooks · doi:10.1002/9781118912591.ch7 · Cited by 11
The transcriptional correlates of divergent electric organ discharges in Paramormyrops electric fish
Losilla, M., Luecke, D. M., & Gallant, J. R. (2020) · BMC Evolutionary Biology · doi:10.1186/s12862-019-1572-3 · Cited by 10
Fowler‐Finn, K. D., Kilmer, J. T., Hallett, A. C., & Rodrı́guez, R. L. (2015) · Ecology and Evolution · doi:10.1002/ece3.1567 · Cited by 9
Blankers, T., Berdan, E. L., Hennig, R. M., & Mayer, F. (2019) · Evolution · doi:10.1111/evo.13706 · Cited by 10
Trajković, J., Pavković‐Lučić, S., Miličić, D., & Savić, T. (2020) · Animal Behaviour · doi:10.1016/j.anbehav.2020.11.005 · Cited by 9
Visual mate preference evolution during butterfly speciation is linked to neural processing genesPreprint
Rossi, M., Hausmann, A. E., Thurman, T. J., Montgomery, S. H., Papa, R., Jiggins, C. D., McMillan, W. O., & Merrill, R. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.22.002121 · Cited by 9
Ellison, C. K., & Shaw, K. L. (2013) · Behavior Genetics · doi:10.1007/s10519-013-9601-2 · Cited by 8
Self-citationThe biogeographic and evolutionary processes shaping population divergence in Laupala
Blankers, T., & Shaw, K. L. (2024) · Molecular Ecology · doi:10.1111/mec.17444 · Cited by 7
Self-citationNegative Coupling: The Coincidence of Premating Isolating Barriers Can Reduce Reproductive IsolationPreprint
Aubier, T. G., Kopp, M., Linn, I. J., Puebla, O., Rafajlović, M., & Servedio, M. R. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041435 · Cited by 8
Gerhardt, H. C. (2015) · Open Access Animal Physiology · doi:10.2147/oaap.s59544 · Cited by 7
Behavioral Evolution: Can You Dig It?
Sheehan, M. J., Miller, C. H., Vogt, C. C., & Ligon, R. A. (2018) · Current Biology · doi:10.1016/j.cub.2017.11.016 · Cited by 6
A framework for studying behavioral evolution by reconstructing ancestral repertoiresPreprint
Hernández, D. G., Rivera, C., Cande, J., Zhou, B., Stern, D. L., & Berman, G. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.17.209361 · Cited by 7
A framework for studying behavioral evolution by reconstructing ancestral repertoires
Hernández, D. G., Rivera, C., Cande, J., Zhou, B., Stern, D. L., & Berman, G. J. (2021) · CONICET Digital (CONICET) · Cited by 6
Whitelaw, B. L., Jones, D. B., Guppy, J. L., Morse, P., Strugnell, J. M., Cooke, I., & Zenger, K. R. (2022) · Diversity · doi:10.3390/d14121068 · Cited by 5
Yukilevich, R. (2022) · Evolution · doi:10.1093/evolut/qpac055 · Cited by 5
Cueva, L., Fuchs, E. J., Barrantes, G., Madrigal‐Brenes, R., & Sandoval, L. (2025) · Ecology and Evolution · doi:10.1002/ece3.70972 · Cited by 3
Temperature effects on interspecific eavesdropping in the wild
Rossi, S. M., Fowler‐Finn, K. D., & Gray, D. A. (2024) · Behavioral Ecology · doi:10.1093/beheco/arae084 · Cited by 3
Kamath, V. G., Mukhopadhyay, A., Alluri, R. K., Acord, A. S., Rose, G. J., & Bee, M. A. (2025) · Journal of Comparative Physiology A · doi:10.1007/s00359-025-01783-0 · Cited by 3
Metadata
- Authors
- Shaw, K. L., & Lesnick, S. C.
- Affiliations
- University of Maryland, College Park (US)
- ORCID
- Shaw, Kerry L.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2009-06-16
- Volume
- 106
- Issue
- 24
- Pages
- 9737-9742
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2701026
- OpenAlex
- W2063512918
- Cited by
- 132
- References
- 45
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 5 · 2023: 1 · 2022: 7 · 2021: 8 · 2020: 7 · 2019: 9 · 2018: 8 · 2017: 7 · 2016: 3 · 2015: 10 · 2014: 10 · 2013: 12 · 2012: 8
- FWCI
- 11.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation
- Topics
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Orthoptera Research and Taxonomy
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Behavior and Reproduction
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Vocal Communication and Behavior
- Keywords
- acoustic communication, male song, quantitative trait loci, species radiation, speciation, sexual selection, female mate choice, mating behavior, sexual isolation, crickets
- MeSH terms
- Animals, Animal Communication, Female, Gryllidae, Genetic Linkage, Male, Phenotype, Quantitative Trait Loci
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review