References
- Allemand, R., & Boulétreau-Merle, J. (1989). Correlated responses in lines of Drosophila melanogaster selected for different oviposition behaviors. Experientia, 45 (11–12), 1147–1150. doi:https://doi.org/10.1007/BF01950184
- Anreiter, I., & Sokolowski, M.B. (2019). The foraging gene and its behavioral effects: Pleiotropy and plasticity. Annual Review of Genetics, 53, 373–392. doi:https://doi.org/10.1146/annurev-genet-112618-043536
- Barker, J.S.F. (1992). Genetic variation in cactophilic drosophila for oviposition on natural yeast substrates. Evolution, 46(4), 1070–1083. doi:https://doi.org/10.1111/j.1558-5646.1992.tb00620.x
- Battesti, M., Moreno, C., Joly, D., & Mery, F. (2012). Spread of social information and dynamics of social transmission within Drosophila groups. Current Biology, 22(4), 309–313. doi:https://doi.org/10.1016/j.cub.2011.12.050
- Becher, P.G., Flick, G., Rozpędowska, E., Schmidt, A., Hagman, A., Lebreton, S., … Bengtsson, M. (2012). Yeast, not fruit volatiles mediate Drosophila melanogaster attraction, oviposition and development. Functional Ecology, 26 (4), 822–828. doi:https://doi.org/10.1111/j.1365-2435.2012.02006.x
- Belay, A.T., Scheiner, R., So, A.K.-C., Douglas, S.J., Chakaborty-Chatterjee, M., Levine, J.D., & Sokolowski, M.B. (2007). The foraging gene of Drosophila melanogaster: spatial-expression analysis and sucrose responsiveness. The Journal of Comparative Neurology, 504 (5), 570–582. doi:https://doi.org/10.1002/cne.21466
- Benelli, G., Daane, K.M., Canale, A., Niu, C.Y., Messing, R.H., & Vargas, R.I. (2014). Sexual communication and related behaviours in Tephritidae: current knowledge and potential applications for Integrated Pest Management. Journal of Pest Science, 87(3), 385–405. doi:https://doi.org/10.1007/s10340-014-0577-3
- Cadieu, N., Ghadraoui, L.E., & Cadieu, J.-C. (2000). Egg-laying preference for ethanol involving learning has adaptive significance in Drosophila melanogaster. Animal Learning & Behavior, 28(2), 187–194. doi:https://doi.org/10.3758/BF03200253
- Chen, Y., & Amrein, H. (2017). Ionotropic receptors mediate Drosophila oviposition preference through sour gustatory receptor neurons. Current Biology, 27 (18), 2741–2750. doi:https://doi.org/10.1016/j.cub.2017.08.003
- Chin, S.G., Maguire, S.E., Huoviala, P., Jefferis, G.S.X.E., & Potter, C.J. (2018). Olfactory neurons and brain centers directing oviposition decisions in Drosophila. Cell Reports, 24 (6), 1667–1678. doi:https://doi.org/10.1016/j.celrep.2018.07.018
- Dason, J.S., Cheung, A., Anreiter, I., Montemurri, V.A., Allen, A.M., & Sokolowski, M.B. (2020). Drosophila melanogaster foraging regulates a nociceptive-like escape behavior through a developmentally plastic sensory circuit. Proceedings of the National Academy of Sciences of the United States of America, 117(38), 23286–23291. doi:https://doi.org/10.1073/pnas.1820840116
- de Belle, J.S., Hilliker, A.J., & Sokolowski, M.B. (1989). Genetic localization of foraging (for): a major gene for larval behavior in Drosophila melanogaster. Genetics, 123 (1), 157–163. doi:https://doi.org/10.1093/genetics/123.1.157
- de Belle, J.S., Sokolowski, M.B., & Hilliker, A.J. (1993). Genetic analysis of the foraging microregion of Drosophila melanogaster. Genome, 36 (1), 94–101. doi:https://doi.org/10.1139/g93-013
- Dukas, R. (2004). Evolutionary biology of animal cognition. Annual Review of Ecology, Evolution, and Systematics, 35 (1), 347–374. doi:https://doi.org/10.1146/annurev.ecolsys.35.112202.130152
- Dukas, R., & Bernays, E.A. (2000). Learning improves growth rate in grasshoppers. Proceedings of the National Academy of Sciences of the United States of America, 97 (6), 2637–2640. doi:https://doi.org/10.1073/pnas.050461497
- Dussutour, A., Deneubourg, J.-L., Beshers, S., & Fourcassié, V. (2009). Individual and collective problem-solving in a foraging context in the leaf-cutting ant Atta colombica. Animal Cognition, 12 (1), 21–30. doi:https://doi.org/10.1007/s10071-008-0165-0
- Edelsparre, A.H., Fitzpatrick, M.J., Rodríguez, M.A., & Sokolowski, M.B. (2021). Tracking dispersal across a patchy landscape reveals a dynamic interaction between genotype and habitat structure. Oikos, 130 (1), 79–94. doi:https://doi.org/10.1111/oik07368
- Edelsparre, A.H., Vesterberg, A., Lim, J.H., Anwari, M., & Fitzpatrick, M.J. (2014). Alleles underlying larval foraging behaviour influence adult dispersal in nature. Ecology Letters, 17(3), 333–339. doi:https://doi.org/10.1111/ele.12234
- Eisses, K.T. (1997). The influence of 2-propanol and acetone on oviposition rate and oviposition site preference for acetic acid and ethanol of Drosophila melanogaster. Behavior Genetics, 27(3), 171–180. doi:https://doi.org/10.1023/A:1025697627556
- Fitzpatrick, M.J., & Szewczyk, E. (2005). Locomotion is not influenced by denticle number in larvae of the fruit fly Drosophila melanogaster. Canadian Journal of Zoology, 83 (2), 368–371. doi:https://doi.org/10.1139/z05-027
- Fitzpatrick, M.J., Feder, E., Rowe, L., & Sokolowski, M.B. (2007). Maintaining a behaviour polymorphism by frequency-dependent selection on a single gene. Nature, 447(7141), 210–212. doi:https://doi.org/10.1038/nature05764
- Frye, M.A., & Dickinson, M.H. (2004). Motor output reflects the linear superposition of visual and olfactory inputs in Drosophila. The Journal of Experimental Biology, 207 (Pt 1), 123–131. doi:https://doi.org/10.1242/jeb.00725
- Giurfa, M. (2013). Cognition with few neurons: higher-order learning in insects. Trends in Neurosciences, 36(5), 285–294. doi:https://doi.org/10.1016/j.tins.2012.12.011
- Gowaty, P.A., Drickamer, L.C., & Schmid-Holmes, S. (2003). Male house mice produce fewer offspring with lower viability and poorer performance when mated with females they do not prefer. Animal Behaviour, 65 (1), 95–103. doi:https://doi.org/10.1006/anbe.2002.2026
- Griffith, L.C., & Ejima, A. (2009). Multimodal sensory integration of courtship stimulating cues in Drosophila melanogaster contextual effects on chemosensory cues. Annals of the New York Academy of Sciences, 1170, 394–398. doi:https://doi.org/10.1111/j.1749-6632.2009.04367.x
- Gruwez, G., Hoste, C., Lints, C.V., & Lints, F.A. (1971). Oviposition rhythm in Drosophila melanogaster and its alteration by a change in the photoperiodicity. Experientia, 27 (12), 1414–1416. doi:https://doi.org/10.1007/BF02154262
- Hughson, B.N., Anreiter, I., Jackson Chornenki, N.L., Murphy, K.R., Ja, W.W., Huber, R., & Sokolowski, M.B. (2018). The adult foraging assay (AFA) detects strain and food-deprivation effects in feeding-related traits of Drosophila melanogaster. Journal of Insect Physiology, 106 (Pt 1), 20–29. doi:https://doi.org/10.1016/j.jinsphys.2017.08.011
- Joseph, R.M., Devineni, A.V., King, I.F.G., & Heberlein, U. (2009). Oviposition preference for and positional avoidance of acetic acid provide a model for competing behavioral drives in Drosophila. Proceedings of the National Academy of Sciences of the United States of America, 106(27), 11352–11357. doi:https://doi.org/10.1073/pnas.0901419106
- Joshi, A., Oshiro, W.A., Shiotsugu, J., & Mueller, L.D. (1997). Within- and among-population variation in oviposition preference for urea-supplemented food in Drosophila melanogaster. Journal of Biosciences, 22(3), 325–338. doi:https://doi.org/10.1007/BF02703235
- Kaun, K.R., Riedl, C.A.L., Chakaborty-Chatterjee, M., Belay, A.T., Douglas, S.J., Gibbs, A.G., & Sokolowski, M.B. (2007). Natural variation in food acquisition mediated via a Drosophila cGMP-dependent protein kinase. The Journal of Experimental Biology, 210(Pt 20), 3547–3558. doi:https://doi.org/10.1242/jeb.006924
- Kawecki, T.J., & Mery, F. (2006). Genetically idiosyncratic responses of Drosophila melanogaster populations to selection for improved learning ability. Journal of Evolutionary Biology, 19(4), 1265–1274. doi:https://doi.org/10.1111/j.1420-9101.2005.01071.x
- Kent, C., Azanchi, R., Smith, B., Formosa, A., & Levine, J.D. (2008). Social context influences chemical communication in D. melanogaster males. Current Biology, 18(18), 1384–1389. doi:https://doi.org/10.1016/j.cub.2008.07.088
- Kent, C.F., Daskalchuk, T., Cook, L., Sokolowski, M.B., & Greenspan, R.J. (2009). The Drosophila foraging gene mediates adult plasticity and gene-environment interactions in behaviour, metabolites, and gene expression in response to food deprivation. PLOS Genetics, 5(8), e1000609. doi:https://doi.org/10.1371/journal.pgen.1000609
- Koseki, T., Koganezawa, M., Furuyama, A., Isono, K., & Shimada, I. (2004). A specific receptor site for glycerol, a new sweet tastant for Drosophila: Structure-taste relationship of glycerol in the labellar sugar receptor cell. Chem Senses, 29 (8), 703–711. doi:https://doi.org/10.1093/chemse/bjh075
- Krupp, J.J., Kent, C., Billeter, J.C., Azanchi, R., So, A.K., Schonfeld, J.A., … Levine, J.D. (2008). Social experience modifies pheromone expression and mating behavior in male Drosophila melanogaster. Current Biology, 18(18), 1373–1383. doi:https://doi.org/10.1016/j.cub.2008.07.089
- Levine, J.D., Pablo, F., Dowse, H.B., & Hall, J.C. (2002). Resetting the circadian clock by social experience in Drosophila melanogaster. Science, 298 (5600), 2010–2012. doi:https://doi.org/10.1126/science.1076008
- Lihoreau, M., Poissonnier, L.A., Isabel, G., & Dussutour, A. (2016). Drosophila females trade off good nutrition with high-quality oviposition sites when choosing foods. The Journal of Experimental Biology, 219 (Pt 16), 2514–2524. doi:https://doi.org/10.1242/jeb.142257
- Maher, N., Thiery, D., & Stadler, E. (2006). Oviposition by Lobesia botrana is stimulated by sugars detected by contact chemoreceptors. Physiological Entomology, 31(1), 14–22. doi:https://doi.org/10.1111/j.1365-3032.2005.00476.x
- Matsuo, T. (2012). Contribution of olfactory and gustatory sensations of octanoic acid in the oviposition behavior of Drosophila melanogaster (Diptera: Drosophilidae). Applied Entomology and Zoology, 47 (2), 137–142. doi:https://doi.org/10.1007/s13355-012-0100-3
- McConnell, M.W., & Fitzpatrick, M.J. (2017). ‘Foraging’ for a place to lay eggs: A genetic link between foraging behaviour and oviposition preferences. PLOS One, 12 (6), e0179362. doi:https://doi.org/10.1371/journal.pone.0179362
- Menzel, R. (2009). Working memory in bees: Also in flies? Journal of Neurogenetics, 23 (1–2), 92–99. doi:https://doi.org/10.1080/01677060802610612
- Mery, F., Varela, S.A., Danchin, E., Blanchet, S., Parejo, D., Coolen, I., & Wagner, R.H. (2009). Public versus personal information for mate copying in an invertebrate. Current Biology, 19(9), 730–734. doi:https://doi.org/10.1016/j.cub.2009.02.064
- Miller, P.M., Saltz, J.B., Cochrane, V.A., Marcinkowski, C.M., Mobin, R., & Turner, T.L. (2011). Natural variation in decision-making behavior in Drosophila melanogaster. PLOS One, 6(1), e16436. doi:https://doi.org/10.1371/journal.pone.0016436
- Morse, D.H., & Stephens, E.G. (1996). The consequences of adult foraging success on the components of lifetime fitness in a semelparous, sit-and-wait predator. Evolutionary Ecology, 10 (4), 361–373. doi:https://doi.org/10.1007/BF01237723
- Naug, D., & Arathi, H.S. (2007). Sampling and decision rules used by honey bees in a foraging arena. Animal Cognition, 10 (2), 117–124. doi:https://doi.org/10.1007/s10071-006-0044-5
- Nilsen, S.P., Chan, Y.B., Huber, R., & Kravitz, E.A. (2004). Gender-selective patterns of aggressive behavior in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the United States of America, 101(33), 12342–12347. doi:https://doi.org/10.1073/pnas.0404693101
- Osborne, K.A., Robichon, A., Burgess, E., Butland, S., Shaw, R.A., Coulthard, A., … Sokolowski, M.B. (1997). Natural behavior polymorphism due to a cGMP-dependent protein kinase of Drosophila. Science, 277 (5327), 834–836. doi:https://doi.org/10.1126/science.277.5327.834
- Pereira, H.S., & Sokolowski, M.B. (1993). Mutations in the larval foraging gene affect adult locomotory behavior after feeding in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the United States of America, 90(11), 5044–5046. doi:https://doi.org/10.1073/pnas.90.11.5044
- Persons, M.H., Walker, S.E., & Rypstra, A.L. (2002). Fitness costs and benefits of antipredator behavior mediated by chemotactile cues in the wolf spider Pardosa milvina (Araneae: Lycosidae). Behavioral Ecology, 13 (3), 386–392. doi:https://doi.org/10.1093/beheco/13.3.386
- Pritchard, G. (1969). The ecology of a natural population of Queensland fruit fly, Dacus tryoni. II. The distribution of eggs and its relation to behaviour. Australian Journal of Zoology, 17 (2), 293–311. doi:https://doi.org/10.1071/ZO9690293
- Ruiz-Dubreuil, D.G., & Köhler, N. (1994). Chromosomal analysis of gregarious oviposition by Drosophila melanogaster. Behavior Genetics, 24(2), 187–190. doi:https://doi.org/10.1007/BF01067823
- Ryuda, M., Calas-List, D., Yamada, A., Marion-Poll, F., Yoshikawa, H., Tanimura, T., & Ozaki, K. (2013). Gustatory sensing mechanism coding for multiple oviposition stimulants in the swallowtail butterfly, Papilio xuthus. The Journal of Neuroscience : The Official Journal of the Society for Neuroscience, 33(3), 914–924. doi:https://doi.org/10.1523/JNEUROSCI.1405-12.2013
- Sarin, S., & Dukas, R. (2009). Social learning about egg-laying substrates in fruitflies. Proceedings. Biological Sciences, 276(1677), 4323–4328. doi:https://doi.org/10.1098/rspb.2009.1294
- Scheiner, R., Sokolowski, M.B., & Erber, J. (2004). Activity of cGMP-dependent protein kinase (PKG) affects sucrose responsiveness and habituation in Drosophila melanogaster. Learning & Memory, 11 (3), 303–311. doi:https://doi.org/10.1101/lm.71604
- Schneider, J., Atallah, J., & Levine, J.D. (2012). One, two, and many-A perspective on what groups of Drosophila melanogaster can tell us about social dynamics. Advances in Genetics, 77, 59–78. doi:https://doi.org/10.1016/B978-0-12-387687-4.00003-9
- Schwartz, N.U., Zhong, L., Bellemer, A., & Tracey, W.D. (2012). Egg laying decisions in Drosophila are consistent with foraging costs of larval progeny. PLOS One, 7(5), e37910. doi:https://doi.org/10.1371/journal.pone.0037910
- Shaver, S.A., Varnam, C.J., Hilliker, A.J., & Sokolowski, M.B. (1998). The foraging gene affects adult but not larval olfactory-related behavior in Drosophila melanogaster. Behavioural Brain Research, 95(1), 23–29. doi:https://doi.org/10.1016/S0166-4328(97)00206-4
- Shelly, T.E. (1999). Defense of oviposition sites by female oriental fruit flies (Diptera: Tephritidae). The Florida Entomologist, 82(2), 339–346. doi:https://doi.org/10.2307/3496587
- Shiraiwa, T., & Carlson, J.R. (2007). Proboscis extension response (PER) assay in Drosophila. Journal of Visualized Experiments, 3 (3), e193. doi:https://doi.org/10.3791/193
- Sokolowski, M.B. (1980). Foraging strategies of Drosophila melanogaster: A chromosomal analysis. Behavior Genetics, 10 (3), 291–302. doi:https://doi.org/10.1007/BF01067774
- Sokolowski, M.B. (2010). Social interactions in “simple” model systems. Neuron, 65(6), 780–794. doi:https://doi.org/10.1016/j.neuron.2010.03.007
- Sokolowski, M.B., & Riedl, C.A.L. (1999). Behavior-genetic and molecular analysis of naturally occurring variation in Drosophila larval foraging behavior. Techniques in the Behavioral and Neural Sciences, 13, 517–532.
- Sokolowski, M.B., Kent, C., & Wong, J. (1984). Drosophila larval foraging behaviour: developmental stages. Animal Behaviour, 32 (3), 645–651. doi:https://doi.org/10.1016/S0003-3472(84)80139-6
- Sokolowski, M.B., Pereira, H.S., & Hughes, K. (1997). Evolution of foraging behavior in Drosophila by density-dependent selection. Proceedings of the National Academy of Sciences of the United States of America, 94 (14), 7373–7377. doi:https://doi.org/10.1073/pnas.94.14.7373
- Stamps, J.A., Yang, L.H., Morales, V.M., & Boundy-Mills, K.L. (2012). Drosophila regulate yeast density and increase yeast community similarity in a natural substrate. PLOS One, 7(7), e42238. doi:https://doi.org/10.1371/journal.pone.0042238
- Tinette, S., Zhang, L., & Robichon, A. (2004). Cooperation between Drosophila flies in searching behavior. Genes, Brain and Behavior, 3 (1), 39–50. doi:https://doi.org/10.1046/j.1601-183x.2003.0046.x
- Ueda, A., & Kidokoro, Y. (2002). Aggressive behaviours of female Drosophila melanogaster are influenced by their social experience and food resources. Physiological Entomology, 27(1), 21–28. doi:https://doi.org/10.1046/j.1365-3032.2002.00262.x
- van Delden, W., & Kamping, A. (1990). Genetic variation for oviposition behavior in Drosophila melanogaster. II. Oviposition preferences and differential survival. Behavior Genetics, 20(5), 661–673. doi:https://doi.org/10.1007/BF01065877
- Loon, J.J.A. (1996). Chemosensory basis of feeding and oviposition behaviour in herbivorous insects: a glance at the periphery. Entomologia Experimentalis et Applicata, 80 (1), 7–13. doi:https://doi.org/10.1111/j.1570-7458.1996.tb00874.x
- van Swinderen, B. (2011). Attention in Drosophila. International Review of Neurobiology, 99, 51–85. doi:https://doi.org/10.1016/B978-0-12-387003-2.00003-3
- Wang, S., & Sokolowski, M.B. (2017). Aggressive behaviours, food deprivation and the foraging gene. Royal Society Open Science, 4(4), 170042. doi:https://doi.org/10.1098/rsos.170042
- Weidt, A., Hofmann, S.E., & König, B. (2008). Not only mate choice matters: fitness consequences of social partner choice in female house mice. Animal Behaviour, 75 (3), 801–808. doi:https://doi.org/10.1016/j.anbehav.2007.06.017
- Wertheim, B. (2005). Evolutionary ecology of communication signals that induce aggregative behaviour. Oikos, 109, 117–124. https://doi.org/https://doi.org/10.1111/j.0030-1299.2005.13340.x
- Wertheim, B., Marchais, J., Vet, L.E.M., & Dick, M. (2002). Allee effect in larval resource exploitation in Drosophila: an interaction among density of adults, larvae, and micro-organisms. Ecological Entomology, 27(5), 608–617. doi:https://doi.org/10.1046/j.1365-2311.2002.00449.x
- Wisotsky, Z., Medina A., Freeman E., – Dahanukar, A. (2011). Evolutionary differences in food preference rely on Gr64e, a receptor for glycerol. Nature Neuroscience, 14: 1543–1541. https://doi.org/https://doi.org/10.1038/nn.2944
- Yang, C.H., Belawat, P., Hafen, E., Jan, L.Y., & Jan, Y.N. (2008). Drosophila egg-laying site selection as a system to study simple decision-making processes. Science, 319(5870), 1679–1683. doi:https://doi.org/10.1126/science.1151842
- Yang, C.H., He, R., & Stern, U. (2015). Behavioral and circuit basis of sucrose rejection by Drosophila females in a simple decision-making task. Journal of Neuroscience, 35(4), 1396–1410. doi:https://doi.org/10.1523/JNEUROSCI.0992-14.2015
- Zhang, L., Yu, J., Guo, X., Wei, J., Liu, T., & Zhang, W. (2020). Parallel mechanosensory pathways direct oviposition decision-making in Drosophila. Current Biology, 30(16), 3075–3088. doi:https://doi.org/10.1016/j.cub.2020.05.076