The Red Queen
1977; University of Chicago Press; Volume: 111; Issue: 980 Linguagem: Inglês
10.1086/283213
ISSN1537-5323
Autores Tópico(s)Polar Research and Ecology
ResumoPrevious articleNext article No AccessLetters to the EditorsThe Red QueenLeigh Van ValenLeigh Van Valen Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 111, Number 980Jul. - Aug., 1977 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/283213 Views: 303Total views on this site Citations: 52Citations are reported from Crossref Copyright 1977 The University of ChicagoPDF download Crossref reports the following articles citing this article:Yalcin Uyar, Ambra Gentile, Hamza Uyar, Övünç Erdeveciler, Hakan Sunay, Veronica Mîndrescu, Dino Mujkic, Antonino Bianco Competition, Gender Equality, and Doping in Sports in the Red Queen Effect Perspective, Sustainability 14, no.55 (Feb 2022): 2490.https://doi.org/10.3390/su14052490Kateryn Pino, Paulo Vallejos-Garrido, Nicolás Espinoza-Aravena, Rebecca B. 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Millar The Influence of Climate Variability and Change on the Science and Practice of Restoration Ecology, (Jan 2016): 484–513.https://doi.org/10.5822/978-1-61091-698-1_17 Distinguished Economic Botanist Award, Economic Botany 68, no.44 (Nov 2014): 365–370.https://doi.org/10.1007/s12231-014-9289-0Edward B. Chuong Retroviruses facilitate the rapid evolution of the mammalian placenta, BioEssays (Jul 2013): n/a–n/a.https://doi.org/10.1002/bies.201300059Mingcong Wang, Maxim V Kapralov, Maria Anisimova Coevolution of amino acid residues in the key photosynthetic enzyme Rubisco, BMC Evolutionary Biology 11, no.11 (Sep 2011).https://doi.org/10.1186/1471-2148-11-266TANIA JENKINS, IAN P. F. OWENS Biogeography of avian blood parasites (Leucocytozoon spp.) in two resident hosts across Europe: phylogeographic structuring or the abundance-occupancy relationship?, Molecular Ecology 20, no.1818 (Aug 2011): 3910–3920.https://doi.org/10.1111/j.1365-294X.2011.05221.xMarta L. Wayne, Jason Pienaar, Marina Telonis-Scott, Lyvie-Sara Sylvestre, Sergey V. Nuzhdin, Lauren M. McIntyre EXPRESSION OF DEFENSE GENES IN DROSOPHILA EVOLVES UNDER A DIFFERENT SELECTIVE REGIME FROM EXPRESSION OF OTHER GENES, Evolution 65, no.44 (Dec 2010): 1068–1078.https://doi.org/10.1111/j.1558-5646.2010.01197.x COMMENTS, The Bulletin of Zoological Nomenclature 67, no.33 (Sep 2010): 243–257.https://doi.org/10.21805/bzn.v67i3.a2P. N. HOEBE, M. STIFT, A. TEDDER, B. K. MABLE Multiple losses of self-incompatibility in North-American Arabidopsis lyrata ?: Phylogeographic context and population genetic consequences, Molecular Ecology 18, no.2323 (Dec 2009): 4924–4939.https://doi.org/10.1111/j.1365-294X.2009.04400.xFlorencio Pazos, Alfonso Valencia Protein co-evolution, co-adaptation and interactions, The EMBO Journal 27, no.2020 (Sep 2008): 2648–2655.https://doi.org/10.1038/emboj.2008.189Pablo A. Marquet, Sebastian R. Abades, Fabio A. Labra Biodiversity power laws, (Jul 2007): 441–461.https://doi.org/10.1017/CBO9780511814938.023Frederic Bouchard Moving beyond the influence of molecular genetics on the debate about reductionism in philosophy of biology, (Jan 2007): 63–80.https://doi.org/10.1007/978-1-4020-5664-2_5Christian O. Marks, Martin J. Lechowicz A holistic tree seedling model for the investigation of functional trait diversity, Ecological Modelling 193, no.3-43-4 (Mar 2006): 141–181.https://doi.org/10.1016/j.ecolmodel.2005.09.011Pablo A. Marquet, Renato A. Quiñones, Sebastian Abades, Fabio Labra, Marcelo Tognelli, Matias Arim, Marcelo Rivadeneira Scaling and power-laws in ecological systems, Journal of Experimental Biology 208, no.99 (May 2005): 1749–1769.https://doi.org/10.1242/jeb.01588D.M. Spratt The role of helminths in the biological control of mammals, International Journal for Parasitology 20, no.44 (Jul 1990): 543–550.https://doi.org/10.1016/0020-7519(90)90202-XSøren Løvtrup On progressive evolution and competitive extinction, Environmental Biology of Fishes 17, no.11 (Sep 1986): 3–12.https://doi.org/10.1007/BF00000396Nils Chr. Stenseth Darwinian Evolution in Ecosystems: A Survey of Some Ideas and Difficulties Together with Some Possible Solutions, (Jan 1986): 105–145.https://doi.org/10.1007/978-3-642-70953-1_5Costas B. Krimbas On Adaptation, Neo-Darwinian Tautology, and Population Fitness, (Jan 1984): 1–57.https://doi.org/10.1007/978-1-4615-6974-9_1Antoni Hoffman, Jennifer A. Kitchell Evolution in a pelagic planktic system: A paleobiologic test of models of multispecies evolution, Paleobiology 10, no.11 (Apr 2016): 9–33.https://doi.org/10.1017/S0094837300007995Carlos Castrodeza Non-progressive evolution, the red queen hypothesis, and the balance of nature, Acta Biotheoretica 28, no.11 (Jan 1979): 11–18.https://doi.org/10.1007/BF00054677Timo Goeschl, Timothy Swanson On the Economic Limits to Technological Potential: Will Industry Resolve the Resistance Problem?, (): 99–128.https://doi.org/10.1007/0-306-47659-2_4
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