Research Articles (Journals)
- . . ‘Genotypes and their interaction effects on reproduction and mating-induced immune activation in Drosophila melanogaster.’ Journal of Evolutionary Biology 00. doi: 10.1111/jeb.13625. [online first]
- . . ‘Sexual conflict drives male manipulation of female postmating responses in Drosophila melanogaster.’ Proceedings of the National Academy of Sciences of the United States of America 116, No. 17: 8437–8444. doi: 10.1073/pnas.1821386116.
- . . ‘Male reproductive ageing - a tale of the whole ejaculate.’ Reproduction 158: R219–R229. doi: 10.1530/REP-18-0579.
- . . ‘Exposure to males, but not receipt of sex peptide, accelerates functional aging in female fruit flies.’ Functional Ecology 33: 1459–1468. doi: 10.1111/1365-2435.13339.
- . . ‘Sexual conflict drives male manipulation of female postmating responses in Drosophila melanogaster.’ PNAS 116, No. 17: 8437–8444. doi: 10.1073/pnas.1821386116.
- . . ‘Divergence in sex peptide-mediated female post-mating responses in Drosophila melanogaster.’ Proceedings of the Royal Society B: Biological Sciences 285, No. 1886. doi: 10.1098/rspb.2018.1563.
- . . ‘The impact of ageing on male reproductive success in Drosophila melanogaster.’ Experimental Gerontology 103: 1–10. doi: 10.1016/j.exger.2017.12.013.
- . . ‘The effect of mating history on male reproductive ageing in Drosophila melanogaster.’ Journal of Insect Physiology 111: 16–24. doi: 10.1016/j.jinsphys.2018.10.003.
- . . ‘Physiological maturation lags behind behavioral maturation in newly eclosed Drosophila melanogaster males.’ Yale Journal of Biology and Medicine 91: 399–408. [accepted / in Press (not yet published)]
- . . ‘Divergence in sex peptide-mediated female post-mating responses in Drosophila melanogaster.’ Proceedings of the Royal Society London B 285. doi: 10.1098/rspb.2018.1563.
- . . ‘Precopulatory but not postcopulatory male reproductive traits diverge in response to mating system manipulation in Drosophila melanogaster.’ Ecology and Evolution 7, No. 23: 10361–10378. doi: 10.1002/ece3.3542.
- . . ‘Precopulatory but not postcopulatory male reproductive traits diverge in response to mating system manipulation in Drosophila melanogaster.’ Ecology and Evolution 7: 10361–10378. doi: 10.1002/ece3.3542.
- . . ‘Gene expression changes in male accessory glands during ageing are accompanied by reproductive decline in Drosophila melanogaster.’ Molecular Ecology 26: 6704–6716. doi: 10.1111/mec.14384.
- . . ‘Variation in the post-mating fitness landscape in fruit flies.’ Journal of Evolutionary Biology 2017, No. 30: 1250–1261. doi: 10.1111/jeb.13090.
- 10.1098/rspb.2016.2394. . ‘Sexual conflict over remating interval is modulated by the sex peptide pathway.’ Proceedings of the Royal Society B 284, No. 20162394. doi:
- . . ‘Early reproductive success in Drosophila males is dependent on maturity of the accessory gland.’ Behavioral Ecology 27, No. 6: 1859–1868. doi: 10.1093/beheco/arw123.
- ‘Early reproductive success in Drosophila males is dependent on maturity of the accessory gland.’ Behavioral Ecology 27, No. 6: 1859–1868. doi: 10.1093/beheco/arw123. .
- . . ‘Effect of competitive cues on reproductive morphology and behavioral plasticity in male fruitflies.’ Behavioral Ecology 27, No. 2: 452–461. doi: 10.1093/beheco/arv170.
- . . ‘The complexity of male reproductive success: effects of nutrition, morphology, and experience.’ Behavioral Ecology 26, No. 2: 617–624. doi: 10.1093/beheco/aru240.
- . . ‘A screen for bacterial endosymbionts in the model organisms Tribolium castaneum, T. confusum, Callosobruchus maculatus and related species.’ Insect Science 22: 165–177. doi: 10.1111/1744-7917.12096.
- . . ‘Prior mating success can affect allocation towards future sexual signaling in crickets.’ PeerJ 657. doi: 10.7717/peerj.657.
- . . ‘MicroRNAs influence reproductive Responses by females to male sex peptide in Drosophila melanogaster.’ Genetics 198: 1603–1619. doi: 10.1534/genetics.114.167320.
- 10.1098/rspb.2013.0428. . ‘Age-dependent female responses to a male ejaculate signal alter demographic opportunities for selection.’ Proceedings of the Royal Society London B 280: 20130428. doi:
- 10.1371/journal.pone.0068136. . ‘Genome-Wide responses of female fruit flies subjected to divergent mating regimes.’ PloS one 8, No. 6: e68136. doi:
- 10.1016/j.exger.2013.03.007. . ‘The lifespan-reproduction trade-off under dietary restriction is sex-specific and context-dependent.’ Experimental Gerontology 48: 539–548. doi:
- . . ‘Interactions between genotype and sexual conflict environment influence transgenerational fitness in drosophila melanogaster.’ Evolution 66, No. 2: 517–531. doi: 10.1111/j.1558-5646.2011.01449.x.
- . . ‘Quantifying the life-history response to increased male exposure in female drosophila melanogaster.’ Evolution 65, No. 2: 564–573. doi: 10.1111/j.1558-5646.2010.01151.x.
- . . ‘Sperm competitive ability and indices of lifetime reproductive success.’ Evolution 64, No. 9: 2746. doi: 10.1111/j.1558-5646.2010.01022.x.
- 10.1111/j.1420-9101.2010.02050.x. . ‘Natural selection hampers divergence of reproductive traits in a seed beetle .’ J. Evol. Biol. 23: 1857–1867. doi:
- 10.1098/rstb.2010.0027. . ‘Adaptations to sexual selection and sexual conflict: insights from experimental evolution and artificial selection .’ Philos. Trans. R. Soc. Lond. B 365: 2541–2548. doi:
- 10.1093/beheco/arp189. . ‘Exposure to rivals and plastic responses to sperm competition in Drosophila melanogaster .’ Behav. Ecol. 21: 317–321. doi:
- 10.1111/j.1420-9101.2009.01882.x. . ‘Female nutritional status determines the magnitude and sign of responses to a male ejaculate signal in Drosophila melanogaster .’ J. Evol. Biol. 23: 157–165. doi:
- 10.1098/rsbl.2009.0433. . ‘The conditional economics of sexual conflict. .’ Biol. Lett. 5: 671–674. doi:
- . ‘Sexual selection did not contribute to the evolution of male lifespan under curtailed age at reproduction in a seed beetle .’ Ecol. Entomol. 34: 638–643.
- 10.1098/rspb.2008.1878. . ‘Plastic responses of male Drosophila melanogaster to the level of sperm competition increase male reproductive fitness.’ Proc. R. Soc. B 276: 1705–1711. doi:
- 10.1111/j.1420-9101.2008.01638.x. . ‘The benefits of male ejaculate sex peptide transfer in Drosophila melanogaster. .’ J. Evol. Biol. 22: 275–286. doi:
- 10.1111/j.1558-5646.2008.00515.x. . ‘Adult male nutrition and reproductive success in Drosophila melanogaster . .’ Evolution 62: 3170.–3177. doi:
- 10.1111/j.1474-9726.2007.00333.x. . ‘Sexual selection affects lifespan and aging in the seed beetle .’ Aging Cell 6: 739–744. doi:
- 10.1016/j.anbehav.2006.12.016. . ‘Male age does not affect female fitness in a polyandrous beetle, Callosobruchus maculatus . .’ Anim. Behav. 74: 541–548. doi:
- 10.1111/j.1558-5646.2007.00038.x. . ‘Rapid adaptation to a novel host in a seed beetle (Callosobruchus maculatus): the role of sexual selection .’ Evolution 61: 440–454. doi:
- 10.1111/j.1365-2435.2006.01102.x. . ‘Female modulation of reproductive rate and its role in postmating prezygotic isolation in Callosobruchus maculatus .’ Funct. Ecol. 20: 360–368. doi:
- 10.1098/rspb.2004.2888. . ‘Sexual selection and the risk of extinction in mammals. .’ Proc. R. Soc. Lond. B 271: 2395–2401. doi:
- 10.1111/j.1420-9101.2004.00757.x. . ‘Divergence in replicated phylogenies: the evolution of partial postmating prezygotic isolation in bean weevils .’ J. Evol. Biol. 17: 1345–1354. doi:
- 10.1016/j.anbehav.2003.08.014. . ‘Conspecific sperm precedence in flour beetles .’ Anim. Behav. 67: 729–732. doi:
- 10.1007/s00265-002-0565-0. . ‘The effects of male and female genotype on variance in male fertilization success in the red flour beetle (Tribolium castaneum) .’ Behav. Ecol. Sociobiol 53, No. 4: 227–233. doi:
- . ‘ Patterns of divergence in the effects of mating on female reproductive performance in flour beetles.’ Evolution 56, No. 1: 111–120.