Publications
292 found
Show per page
Mathieu-Bégné, E., Gattis, S., & Ebert, D. (2024). Genetic basis of resistance in hosts facing alternative infection strategies by a virulent bacterial pathogen [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.08.15.607931
Naser-Khdour, S., Scheuber, F., Fields, P. D., & Ebert, D. (2024). The Evolution of Extreme Genetic Variability in a Parasite-Resistance Complex in a Planktonic Crustacean [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.08.09.607325
Joana L. Santos, Fabienne Nick, Nikko Adhitama, Peter D. Fields, Jonathon H. Stillman, Yasuhiko Kato, Hajime Watanabe, & Current Biology, 34(18). https://doi.org/10.1016/j.cub.2024.07.082
. (2024). Trehalose mediates salinity-stress tolerance in natural populations of a freshwater crustacean. Santhosh, Santhosh, Journal of Evolutionary Biology, 37(7), 829–838. https://doi.org/10.1093/jeb/voae058
, & Janicke, Tim. (2024). Sperm competition favours intermediate sperm size in a hermaphrodite [Journal-article]. Angst, Pascal, Haag, Christoph R, Ben-Ami, Frida, Fields, Peter D, & Molecular Biology and Evolution, 41(7). https://doi.org/10.1093/molbev/msae128
. (2024). Genome-Wide Allele Frequency Changes Reveal That Dynamic Metapopulations Evolve Differently [Journal-article]. Otte, Kathrin A., Fredericksen, Maridel, Fields, Peter, Fröhlich, Thomas, Laforsch, Christian, & PROTEOMICS, 24(14). https://doi.org/10.1002/pmic.202300292
. (2024). The cuticle proteome of a planktonic crustacean [Journal-article]. Cornetti, Luca, Fields, Peter D., Du Pasquier, Louis, & Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-49726-8
. (2024). Long-term balancing selection for pathogen resistance maintains trans-species polymorphisms in a planktonic crustacean [Journal-article]. Huessy, B., Bumann, D., & Ebert, D. (2024). Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution. Royal Society Open Science, 11(4). https://doi.org/10.1098/rsos.231441
Van de Schoot, Evert, Merckx, Thomas, Biology Letters, 20(3). https://doi.org/10.1098/rsbl.2023.0486
, Wesselingh, Renate A., Altermatt, Florian, & Van Dyck, Hans. (2024). Evolutionary change in flight-to-light response in urban moths comes with changes in wing morphology [Journal-article]. Santos, J. L., Nick, F., Adhitama, N., Fields, P. D., Stillman, J. H., Kato, Y., Watanabe, H., & Ebert, D. (2024). Trehalose mediates salinity-stress tolerance in a crustacean [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.02.09.579427
Thivolle, A., Paljakka, M., Ebert, D., & Fields, P. D. (2024). The genome of Pasteuria ramosa reveals a high turnover rate of collagen-like genes [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.02.09.579640
Angst, P., Haag, C. R., Ben-Ami, F., Fields, P. D., & Ebert, D. (2024, January 20). Genome-wide allele frequency changes reveal that dynamic metapopulations evolve differently [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2024.01.18.575980
Angst, Pascal, & BioSpektrum, 30, 49–51. https://doi.org/10.1007/s12268-024-2080-6
. (2024). Mikrosporidien-Genome als Fenster zu deren Evolution. Angst, Pascal, Ameline, Camille, Haag, Christoph R., Ben-Ami, Frida, Molecular Biology and Evolution, 39(12), msac264. https://doi.org/10.1093/molbev/msac264
, & Fields, Peter D. (2023). Genetic Drift Shapes the Evolution of a Highly Dynamic Metapopulation. Angst, Pascal, G3: Genes, Genomes, Genetics, 13. https://doi.org/10.1093/g3journal/jkad017
, & Fields, Peter D. (2023). Population genetic analysis of the microsporidium Ordospora colligata reveals the role of natural selection and phylogeography on its extremely compact and reduced genome. Angst, Pascal, Pombert, Jean-François, G3: Genes, Genomes, Genetics, 13. https://doi.org/10.1093/g3journal/jkad185
, & Fields, Peter D. (2023). Near chromosome-level genome assembly of the microsporidium Hamiltosporidium tvaerminnensis. Dexter, Eric, Fields, Peter D., & Molecular Biology and Evolution, 40. https://doi.org/10.1093/molbev/msad145
. (2023). Uncovering the Genomic Basis of Infection Through Co-genomic Sequencing of Hosts and Parasites. Fredericksen, Maridel, Fields, Peter D., Du Pasquier, Louis, Ricci, Virginie, & PLoS Genetics, 19. https://doi.org/10.1371/journal.pgen.1010570
. (2023). QTL study reveals candidate genes underlying host resistance in a Red Queen model system. Huessy, Benjamin, Bumann, Dirk, & Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host-parasite coevolution. bioRxiv. https://doi.org/10.1101/2023.07.14.549037
. (2023). Santos, Joana L., & Oecologia, 203, 453–465. https://doi.org/10.1007/s00442-023-05478-8
. (2023). The limits of stress-tolerance for zooplankton resting stages in freshwater ponds. Tadiri, Christina P., & Oikos, 2023. https://doi.org/10.1111/oik.10014
. (2023). The role of temperature in the start of seasonal infectious disease epidemics. Dexter, E., Fields, P. D., & Ebert, D. (2022, December 8). Uncovering the genomic basis of infection through co-genomic sequencing of hosts and parasites [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2022.12.05.519109
Halter, M., Du Pasquier, L., Ebert, D., & Fields, P. D. (2022, March 13). A genomic analysis of parasite-mediated population differentiation in a metapopulation [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2022.03.10.483675
Amandine, Cornille, Trends in Genetics, 38(10), 1003–1012. https://doi.org/10.1016/j.tig.2022.05.008
, Stukenbrock, Eva, Rodríguez de la Vega, Ricardo C., Tiffin, Peter, Croll, Daniel, & Tellier, Aurélien. (2022). Unraveling coevolutionary dynamics using ecological genomics. Ameline, Camille, Voegtli, Felix, Andras, Jason, Dexter, Eric, Engelstädter, Jan, & Science Advances, 8(46), eabn0051. https://doi.org/10.1126/sciadv.abn0051
. (2022). Genetic slippage after sex maintains diversity for parasite resistance in a natural host population. Angst, Pascal, Molecular Ecology, 31(9), 2528–2544. https://doi.org/10.1111/mec.16419
, & Fields, Peter D. (2022). Demographic history shapes genomic variation in an intracellular parasite with a wide geographical distribution. de Albuquerque, Nathalia R. M., Haag, Karen L., Fields, Peter D., Cabalzar, Andrea, Ben-Ami, Frida, Pombert, Jean-François, & The Journal of Eukaryotic Microbiology, 69(3), e12902. https://doi.org/10.1111/jeu.12902
. (2022). A new microsporidian parasite, Ordospora pajunii sp. nov (Ordosporidae), of Daphnia longispina highlights the value of genomic data for delineating species boundaries. Duneau, David, Möst, Markus, & Peer Community Journal, 2, e63. https://doi.org/10.24072/pcjournal.182
. (2022). Evolution of sperm morphology in a crustacean genus with fertilization inside an open brood pouch. EvoDevo, 13(1), 16. https://doi.org/10.1186/s13227-022-00199-0
. (2022). Daphnia as a versatile model system in ecology and evolution. Fields, Peter D., McTaggart, Seanna, Reisser, Céline M. O., Haag, Christoph, Palmer, William H., Little, Tom J., Molecular Biology and Evolution, 39(3), msac048. https://doi.org/10.1093/molbev/msac048
, & Obbard, Darren J. (2022). Population-Genomic Analysis Identifies a Low Rate of Global Adaptive Fixation in the Proteins of the Cyclical Parthenogen Daphnia magna. Heim, Vital, Luescher, Daniel, Hottinger, Juergen, & Animal Biotelemetry, 10(1), ARTN 33. https://doi.org/10.1186/s40317-022-00304-z
. (2022). Development and validation of a drill attachment for faster and safer deployments of fin-mounted geolocators in large-bodied sharks. Luo, Mingyu, Wang, Shaopeng, Saavedra, Serguei, Proceedings of the National Academy of Sciences of the United States of America, 119(37), e2201503119. https://doi.org/10.1073/pnas.2201503119
, & Altermatt, Florian. (2022). Multispecies coexistence in fragmented landscapes. Santos, Joana L., & Journal of Freshwater Ecology, 37(1), 555–568. https://doi.org/10.1080/02705060.2022.2134219
. (2022). The effects of temperature and host-parasite interactions on parasite persistence in a planktonic crustacean. Santos, Joana L., & Biology Letters, 18(2), 20210615. https://doi.org/10.1098/rsbl.2021.0615
. (2022). Trehalose provisioning in Daphnia resting stages reflects local adaptation to the harshness of diapause conditions. Van Damme, Kay, Cornetti, Luca, Fields, Peter D., & Systematic Biology, 71(4), 777–787. https://doi.org/10.1093/sysbio/syab094
. (2022). Whole-Genome Phylogenetic Reconstruction as a Powerful Tool to Reveal Homoplasy and Ancient Rapid Radiation in Waterflea Evolution. Haaland, T. R., Ebert, D., & Kokko, H. (2021, October 22). Sex differences in the strength of selection under facultative sex [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2021.10.21.465271
Ameline, C., Vögtli, F., Andras, J., Dexter, E., Engelstädter, J., & Ebert, D. (2021, July 12). Genetic slippage after sex maintains diversity for parasite resistance in a natural host population [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2021.07.11.451958
Ameline, Camille, Bourgeois, Yann, Vögtli, Felix, Savola, Eevi, Andras, Jason, Engelstädter, Jan, & Molecular Biology and Evolution, 38(4), 1512–1528. https://doi.org/10.1093/molbev/msaa311
. (2021). A two-locus system with strong epistasis underlies rapid parasite-mediated evolution of host resistance. Ameline, Camille, Bourgeois, Yann, Vögtli, Felix, Savola, Eevi, Andras, Jason, Engelstädter, Jan, & Molecular Biology and Evolution, 38(6), 2674. https://doi.org/10.1093/molbev/msab076
. (2021). Erratum to: A Two-Locus System with Strong Epistasis Underlies Rapid Parasite-Mediated Evolution of Host Resistance. Bourgeois, Yann, Fields, Peter D., Bento, Gilberto, & Molecular Biology and Evolution, 38(11), 4918–4933. https://doi.org/10.1093/molbev/msab217
. (2021). Balancing Selection for Pathogen Resistance Reveals an Intercontinental Signature of Red Queen Coevolution. Cornetti, Luca, & Royal Society Open Science, 8(6), 202292. https://doi.org/10.1098/rsos.202292
. (2021). No evidence for genetic sex determination in Daphnia magna. Cornetti, Luca, Fields, Peter D., & Journal of Evolutionary Biology, 34(5), 792–802. https://doi.org/10.1111/jeb.13780
. (2021). Genomic characterization of selfing in the cyclic parthenogen Daphnia magna. Fredericksen, Maridel, Ameline, Camille, Krebs, Michelle, Hüssy, Benjamin, Fields, Peter D., Andras, Jason P., & Evolution: International Journal of Organic Evolution, 75(10), 2540–2554. https://doi.org/10.1111/evo.14323
. (2021). Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific. Vega, Fernando E., Emche, Sarah, Shao, Jonathan, Simpkins, Ann, Summers, Ryan M., Mock, Meredith B., Frontiers in Microbiology, 12, 644768. https://doi.org/10.3389/fmicb.2021.644768
, Infante, Francisco, Aoki, Sayaka, & Maul, Jude E. (2021). Cultivation and Genome Sequencing of Bacteria Isolated From the Coffee Berry Borer (Hypothenemus hampei), With Emphasis on the Role of Caffeine Degradation. Dubart, M., David, P., Ben-Ami, F., Haag, C. R., Pajunen, V. I., & Ebert, D. (2020, July 10). Species coexistence and overlapping distributions in a metacommunity are compatible with niche differences and competition at a local scale [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.07.10.196758
Ameline, C., Bourgeois, Y., Vögtli, F., Savola, E., Andras, J., Engelstädter, J., & Ebert, D. (2020, June 12). A two-locus system with strong epistasis underlies rapid parasite-mediated evolution of host resistance [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.06.11.145391
Duneau, D., Altermatt, F., Ferdy, J.-B., Ben-Ami, F., & Ebert, D. (2020, February 5). Estimation of the propensity for sexual selection in a cyclical parthenogen [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.02.05.935148
Duneau, D., Möst, M., & Ebert, D. (2020, February 2). Evolution of sperm morphology in a crustacean genus with fertilization inside an open brood pouch [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.01.31.929414
Andras, Jason P., Fields, Peter D., Du Pasquier, Louis, Fredericksen, Maridel, & Molecular Biology and Evolution, 37(12), 3439–3452. https://doi.org/10.1093/molbev/msaa173
. (2020). Genome-Wide Association Analysis Identifies a Genetic Basis of Infectivity in a Model Bacterial Pathogen. Bento, Gilberto, Fields, Peter D., Duneau, David, & Heredity, 125(4), 173–183. https://doi.org/10.1038/s41437-020-0332-x
. (2020). An alternative route of bacterial infection associated with a novel resistance locus in the Daphnia-Pasteuria host-parasite system. de Albuquerque, Nathalia Rammé Medeiros, Mobile DNA, 11, 19. https://doi.org/10.1186/s13100-020-00218-8
, & Haag, Karen Luisa. (2020). Transposable element abundance correlates with mode of transmission in microsporidian parasites. Nature reviews. Genetics, 21(12), 754–768. https://doi.org/10.1038/s41576-020-0269-1
, & Fields, Peter D. (2020). Host-parasite co-evolution and its genomic signature. Haag, Karen L., Pombert, Jean-François, Sun, Yukun, de Albuquerque, Nathalia Rammé M., Batliner, Brendan, Fields, Peter, Lopes, Tiago Falcon, & Genome Biology and Evolution, 12(1), 3599–3614. https://doi.org/10.1093/gbe/evz270
. (2020). Microsporidia with Vertical Transmission Were Likely Shaped by Nonadaptive Processes. Ho, Eddie K. H., Macrae, Fenner, Latta, Leigh C., McIlroy, Peter, Molecular Biology and Evolution, 37(11), 3258–3266. https://doi.org/10.1093/molbev/msaa142
, Fields, Peter D., Benner, Maia J., & Schaack, Sarah. (2020). High and Highly Variable Spontaneous Mutation Rates in Daphnia. Cabalzar, A. P., Fields, P. D., Kato, Y., Watanabe, H., & Ebert, D. (2019). Parasite-mediated selection in a natural metapopulation of Daphnia magna. Molecular Ecology, 28(21), 4770–4785. https://doi.org/10.1111/mec.15260
Brun, Nadja R., Fields, Peter D., Horsfield, Samuel, Mirbahai, Leda, Environmental Science and Technology, 53(3), 1639–1649. https://doi.org/10.1021/acs.est.8b05457
, Colbourne, John K., & Fent, Karl. (2019). Mixtures of Aluminum and Indium Induce More than Additive Phenotypic and Toxicogenomic Responses in Daphnia magna. Cornetti, Luca, Fields, Peter D., Van Damme, Kay, & Molecular Phylogenetics and Evolution, 137, 250–262. https://doi.org/10.1016/j.ympev.2019.05.018
. (2019). A fossil-calibrated phylogenomic analysis of Daphnia and the Daphniidae. Czypionka, Till, Fields, Peter D., Routtu, Jarkko, van den Berg, Edwin, Molecular Ecology, 28(5), 998–1008. https://doi.org/10.1111/mec.15001
, & De Meester, Luc. (2019). The genetic architecture underlying diapause termination in a planktonic crustacean. Dukić, Marinela, Berner, Daniel, Haag, Christoph R., & Journal of Evolutionary Biology, 32(6), 619–628. https://doi.org/10.1111/jeb.13443
. (2019). How clonal are clones? A quest for loss of heterozygosity during asexual reproduction in Daphnia magna. Hall, Matthew D., Routtu, Jarkko, & Molecular Ecology, 28(17), 3942–3957. https://doi.org/10.1111/mec.15166
. (2019). Dissecting the genetic architecture of a stepwise infection process. Ho, Eddie K. H., Macrae, Fenner, Latta, Leigh C., Benner, Maia J., Sun, Cheng, Molecular Biology and Evolution, 36(9), 1942–1954. https://doi.org/10.1093/molbev/msz118
, & Schaack, Sarah. (2019). Intraspecific Variation in Microsatellite Mutation Profiles in Daphnia magna. Martin-Creuzburg, Dominik, Coggins, B. L., Physiological and Biochemical Zoology, 92(4), 408–418. https://doi.org/10.1086/704365
, & Yampolsky, Lev Y. (2019). Rearing Temperature and Fatty Acid Supplementation Jointly Affect Lipid Fluorescence Polarization and Heat Tolerance in Daphnia. Mushegian, Alexandra A., Arbore, Roberto, Walser, Jean-Claude, & Dryad, 1. https://doi.org/10.5061/dryad.g75r459
. (2019). Data from: Environmental sources of bacteria and genetic variation in behavior influence host-associated microbiota. Mushegian, Alexandra A., Arbore, Roberto, Walser, Jean-Claude, & Applied and Environmental Microbiology, 85(8), e01547–18. https://doi.org/10.1128/aem.01547-18
. (2019). Environmental Sources of Bacteria and Genetic Variation in Behavior Influence Host-Associated Microbiota. Narr, Charlotte F., Journal of Animal Ecology, 88(4), 579–590. https://doi.org/10.1111/1365-2656.12945
, Bastille-Rousseau, Guillaume, & Frost, Paul C. (2019). Nutrient availability affects the prevalence of a microsporidian parasite. Savola, Eevi, & BMC Ecology, 19(1), 14. https://doi.org/10.1186/s12898-019-0230-3
. (2019). Assessment of parasite virulence in a natural population of a planktonic crustacean. Seefeldt, Leonie, & Proceedings of the Royal Society. Series B, Biological Sciences, 286(1907), 20190929. https://doi.org/10.1098/rspb.2019.0929
. (2019). Temperature - versus precipitation-limitation shape local temperature tolerance in a Holarctic freshwater crustacean. Martin-Creuzburg, D., Coggins, B. L., Rearing temperature and fatty acid supplementation jointly affect membrane fluidity and heat tolerance in<i>Daphnia</i> [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/295998
, & Yampolsky, L. Y. (2018, April 6). Mushegian, A. A., Arbore, R., Walser, J.-C., & Ebert, D. (2018, April 6). Environmental sources of bacteria and genetic variation in behavior influence host-associated microbiota [Posted-content]. Cold Spring Harbor Laboratory. https://doi.org/10.1101/296228
Andras, Jason P., Fields, Peter D., & Molecular Ecology, 27(6), 1371–1384. https://doi.org/10.1111/mec.14545
. (2018). Spatial population genetic structure of a bacterial parasite in close coevolution with its host. Booksmythe, Isobel, Gerber, Nina, Ecology Letters, 21(5), 629–637. https://doi.org/10.1111/ele.12929
, & Kokko, Hanna. (2018). Daphnia females adjust sex allocation in response to current sex ratio and density. Ebert, Bettina, Febs Journal, 285(15), 2869–2887. https://doi.org/10.1111/febs.14578
, Koebsch, Katrin, Maser, Edmund, & Kisiela, Michael. (2018). Carbonyl reductases from Daphnia are regulated by redox cycling compounds. BMC Biology, 16(1), 114. https://doi.org/10.1186/s12915-018-0583-7
. (2018). Open questions: what are the genes underlying antagonistic coevolution? Fields, Peter D., Obbard, Darren J., McTaggart, Seanna J., Galimov, Yan, Little, Tom J., & Molecular Phylogenetics and Evolution, 129, 138–148. https://doi.org/10.1016/j.ympev.2018.06.028
. (2018). Mitogenome phylogeographic analysis of a planktonic crustacean. Gerber, Nina, Kokko, Hanna, Proceedings of the Royal Society B-Biological Sciences, 285(1871), 1–9. https://doi.org/10.1098/rspb.2017.2176
, & Booksmythe, Isobel. (2018). Daphnia invest in sexual reproduction when its relative costs are reduced. Mushegian, Alexandra, Walser, Jean-Claude, Sullam, Karen E., & Journal of Animal Ecology, 87(2), 400–413. https://doi.org/10.1111/1365-2656.12709
. (2018). The microbiota of diapause: how host-microbe associations are formed after dormancy in an aquatic crustacean. Preiswerk, David, Walser, Jean-Claude, & Isme Journal, 12(8), 2076–2085. https://doi.org/10.1038/s41396-018-0157-2
. (2018). Temporal dynamics of microbiota before and after host death. Sison-Mangus, Marilou P., Metzger, César M. J. A., & Scientific Reports, 8(1), 9407. https://doi.org/10.1038/s41598-018-27681-x
. (2018). Host genotype-specific microbiota do not influence the susceptibility of D. magna to a bacterial pathogen. Sullam, Karen E., Pichon, Samuel, Schaer, Tobias M. M., & Microbial Ecology, 76(2), 506–517. https://doi.org/10.1007/s00248-017-1126-4
. (2018). The Combined Effect of Temperature and Host Clonal Line on the Microbiota of a Planktonic Crustacean. Toenshoff, Elena R., Fields, Peter D., Bourgeois, Yann X., & G3-Genes Genomes Genetics, 8(4), 1259–1272. https://doi.org/10.1534/g3.117.300429
. (2018). The End of a 60-year Riddle: Identification and Genomic Characterization of an Iridovirus, the Causative Agent of White Fat Cell Disease in Zooplankton. Bento, Gilberto, Routtu, Jarkko, Fields, Peter D., Bourgeois, Yann X., Du Pasquier, Louis, & PLoS Genetics, 13(2), e1006596. https://doi.org/10.1371/journal.pgen.1006596
. (2017). The genetic basis of resistance and matching-allele interactions of a host-parasite system: The Daphnia magna-Pasteuria ramosa model. Bourgeois, Yann X., Roulin, Anne C., Muller, Kristina, & Evolution, 71(4), 1106–1113. https://doi.org/10.1111/evo.13209
. (2017). Parasitism drives host genome evolution: Insights from the Pasteuria ramosa-Daphnia magna system. Brun, Nadja R., Beenakker, Margreet M. T., Hunting, Ellard R., Nanotoxicology, 11(8), 1059–1069. https://doi.org/10.1080/17435390.2017.1391344
, & Vijver, Martina G. (2017). Brood pouch-mediated polystyrene nanoparticle uptake during Daphnia magna embryogenesis. Hall, Matthew D., Bento, Gilberto, & Trends in Ecology & Evolution, 32(8), 612–623. https://doi.org/10.1016/j.tree.2017.05.009
. (2017). The Evolutionary Consequences of Stepwise Infection Processes. Krebs, Michelle, Routtu, Jarkko, & Parasitology, 144(13), 1686–1694. https://doi.org/10.1017/s0031182017001032
. (2017). QTL mapping of a natural genetic polymorphism for long-term parasite persistence in Daphnia populations. Mushegian, Alexandra A., & Zoology, 125, 29–31. https://doi.org/10.1016/j.zool.2017.07.007
. (2017). Presence of microbiota reverses the relative performance of Daphnia on two experimental diet. Psychological Medicine, 46(13), 2679–2693. https://doi.org/10.1017/s0033291716001562
, Donkin, L., Andersson, G., Andrews, G., Berger, T., Carlbring, P., Rozenthal, A., Choi, I., Laferton, J.A.C., Johansson, R., Kleiboer, A., Lange, A., Lehr, D., Reins, J.A., Funk, B., Newby, J., Perini, S., Riper, H., Ruwaard, J., et al. (2016). Does Internet-based guided-self-help for depression cause harm? An individual participant data meta-analysis on deterioration rates and its moderators in randomized controlled trials. Altermatt, Florian, & Biology Letters, 12(4), 20160111. https://doi.org/10.1098/rsbl.2016.0111
. (2016). Reduced flight-to-light behaviour of moth populations exposed to long-term urban light pollution. Arbore, R., Andras, J. P., Routtu, J., & Journal of Evolutionary Biology, 29(10), 1999–2009. https://doi.org/10.1111/jeb.12923
. (2016). Ecological genetics of sediment browsing behaviour in a planktonic crustacean. Dukić, Marinela, Berner, Daniel, Roesti, Marius, Haag, Christoph R., & BMC genetics, 17(1), 137. https://doi.org/10.1186/s12863-016-0445-7
. (2016). A high-density genetic map reveals variation in recombination rate across the genome of Daphnia magna. Duneau, David, Developmental and Comparative Immunology, 57, 120–125. https://doi.org/10.1016/j.dci.2015.12.004
, & Du Pasquier, Louis. (2016). Infections by Pasteuria do not protect its natural host Daphnia magna from subsequent infections. Advances in Parasitology, 91, 265–+. https://doi.org/10.1016/bs.apar.2015.10.001
, Duneau, David, Hall, Matthew D., Luijckx, Pepijn, Andras, Jason P., Du Pasquier, Louis, & Ben-Ami, Frida. (2016). A Population Biology Perspective on the Stepwise Infection Process of the Bacterial Pathogen Pasteuria ramosa in Daphnia. Metzger, César M. J. A., Luijckx, Pepijn, Bento, Gilberto, Mariadassou, Mahendra, & Evolution, 70(2), 480–487. https://doi.org/10.1111/evo.12854
. (2016). The Red Queen lives: Epistasis between linked resistance loci. Michel, Jessica, BMC Evolutionary Biology, 16(1), 254. https://doi.org/10.1186/s12862-016-0828-4
, & Hall, Matthew D. (2016). The trans-generational impact of population density signals on host-parasite interactions. Mushegian, Alexandra A., Burcklen, Elodie, Schär, Tobias M. M., & Journal of Experimental Biology, 219(Pt 6), 897–904. https://doi.org/10.1242/jeb.134759
. (2016). Temperature-dependent benefits of bacterial exposure in embryonic development of Daphnia magna resting eggs. Mushegian, Alexandra A, & Bioessays, 38(1), 100–108. https://doi.org/10.1002/bies.201500074
. (2016). Rethinking “mutualism” in diverse host-symbiont communities. Orsini, Luisa, Gilbert, Donald, Podicheti, Ram, Jansen, Mieke, Brown, James B., Solari, Omid Shams, Spanier, Katina I., Colbourne, John K., Rush, Douglas, Decaestecker, Ellen, Asselman, Jana, De Schamphelaere, Karel A. C., Scientific Data, 4, 160030. https://doi.org/10.1038/sdata.2016.30
, Haag, Christoph R., Kvist, Jouni, Laforsch, Christian, Petrusek, Adam, Beckerman, Andrew P., Little, Tom J., et al. (2016). Daphnia magna transcriptome by RNA-Seq across 12 environmental stressors. Rabajante, Jomar F., Tubay, Jerrold M., Ito, Hiromu, Uehara, Takashi, Kakishima, Satoshi, Morita, Satoru, Yoshimura, Jin, & Science Advances, 2(3), e1501548. https://doi.org/10.1126/sciadv.1501548
. (2016). Host-parasite Red Queen dynamics with phase-locked rare genotypes. Retnaningdyah, C., & Journal of Tropical Life Science, 6, 136–141. https://doi.org/10.11594/jtls.06.03.0
. (2016). Bleach Solution Requirement for Hatching of Daphnia magna Resting Eggs. Roulin, Anne C., Bourgeois, Yann, Stiefel, Urs, Walser, Jean-Claude, & Molecular Biology and Evolution, 33(12), 3194–3204. https://doi.org/10.1093/molbev/msw200
. (2016). A Photoreceptor Contributes to the Natural Variation of Diapause Induction in Daphnia magna.