Observations on Structural Reduction in Evolution
1964; University of Chicago Press; Volume: 98; Issue: 901 Linguagem: Inglês
10.1086/282323
ISSN1537-5323
Autores Tópico(s)Evolution and Genetic Dynamics
ResumoPrevious articleNext article No AccessObservations on Structural Reduction in EvolutionTimothy ProutTimothy ProutPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 98, Number 901Jul. - Aug., 1964 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/282323 Views: 19Total views on this site Citations: 32Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Joseph Jalinsky, John M. Logsdon, Maurine Neiman Male phenotypes in a female framework: Evidence for degeneration in sperm produced by male snails from asexual lineages, Journal of Evolutionary Biology 33, no.88 (May 2020): 1050–1059.https://doi.org/10.1111/jeb.13632Henry D. Legett, Rachel A. Page, Ximena E. 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GARDNER Functional innovation through vestigialization in a modular marine invertebrate, Biological Journal of the Linnean Society 104, no.11 (Aug 2011): 63–74.https://doi.org/10.1111/j.1095-8312.2011.01706.xSajid Ali, Marc Leconte, Anne-Sophie Walker, Jérôme Enjalbert, Claude de Vallavieille-Pope Reduction in the sex ability of worldwide clonal populations of Puccinia striiformis f.sp. tritici, Fungal Genetics and Biology 47, no.1010 (Oct 2010): 828–838.https://doi.org/10.1016/j.fgb.2010.07.002David C. Lahti, Norman A. Johnson, Beverly C. Ajie, Sarah P. Otto, Andrew P. Hendry, Daniel T. Blumstein, Richard G. Coss, Kathleen Donohue, Susan A. Foster Relaxed selection in the wild, Trends in Ecology & Evolution 24, no.99 (Sep 2009): 487–496.https://doi.org/10.1016/j.tree.2009.03.010Enrique Rodríguez-Serrano, R. Eduardo Palma, Cristián E. Hernández The evolution of ecomorphological traits within the Abrothrichini (Rodentia: Sigmodontinae): A bayesian phylogenetics approach, Molecular Phylogenetics and Evolution 48, no.22 (Aug 2008): 473–480.https://doi.org/10.1016/j.ympev.2008.05.012David W. Stock Zebrafish dentition in comparative context, Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 308B, no.55 (Jan 2007): 523–549.https://doi.org/10.1002/jez.b.21187M. E. Dorken, K. J. Neville, C. G. Eckert Evolutionary vestigialization of sex in a clonal plant: selection versus neutral mutation in geographically peripheral populations, Proceedings of the Royal Society of London. 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BRUCE CAMPBELL Single rays as indicators of fin vestigialization in coho salmon: patterns and perspectives, Biological Journal of the Linnean Society 71, no.44 (Jan 2008): 789–799.https://doi.org/10.1111/j.1095-8312.2000.tb01291.xWilliam G. Eberhard Breaking the mold: behavioral variation and evolutionary innovation in Wendilgarda spiders (Araneae Theridiosomatidae), Ethology Ecology & Evolution 12, no.33 (Jul 2000): 223–235.https://doi.org/10.1080/08927014.2000.9522797Christopher G. Eckert, Marcel E. Dorken, Stacy A. Mitchell LOSS OF SEX IN CLONAL POPULATIONS OF A FLOWERING PLANT, DECODON VERTICILLATUS (LYTHRACEAE), Evolution 53, no.44 (May 2017): 1079–1092.https://doi.org/10.1111/j.1558-5646.1999.tb04523.xRobert G. Tague VARIABILITY OF A VESTIGIAL STRUCTURE: FIRST METACARPAL IN COLOBUS GUEREZA AND ATELES GEOFFROYI, Evolution 51, no.22 (May 2017): 595–605.https://doi.org/10.1111/j.1558-5646.1997.tb02446.x Costs to host defence and the persistence of parasitic cuckoos, Proceedings of the Royal Society of London. Series B: Biological Sciences 248, no.13211321 (Jan 1997): 41–45.https://doi.org/10.1098/rspb.1992.0040Douglas J. Futuyma Anpassung, (Jan 1990): 283–322.https://doi.org/10.1007/978-3-0348-5235-7_9James M. Calcagno, Kathleen R. Gibson Human dental reduction: Natural selection or the probable mutation effect, American Journal of Physical Anthropology 77, no.44 (Dec 1988): 505–517.https://doi.org/10.1002/ajpa.1330770411Paul W. Sciulli, Charles Janini, Myra Giesen Phenotypic selection on the dentition in a late archaic population of Ohio, American Journal of Physical Anthropology 76, no.44 (Aug 1988): 527–533.https://doi.org/10.1002/ajpa.1330760412C. Loring Brace, Karen R. Rosenberg, Kevin D. Hunt GRADUAL CHANGE IN HUMAN TOOTH SIZE IN THE LATE PLEISTOCENE AND POST-PLEISTOCENE, Evolution 41, no.44 (May 2017): 705–720.https://doi.org/10.1111/j.1558-5646.1987.tb05847.xJeffrey K. McKee A genetic model of dental reduction through the probable mutation effect, American Journal of Physical Anthropology 65, no.33 (Nov 1984): 231–241.https://doi.org/10.1002/ajpa.1330650302C.E. Yarwood Host Passage Effects with Plant Viruses, (Jan 1979): 169–190.https://doi.org/10.1016/S0065-3527(08)60570-9 Philip J. Regal Evolutionary Loss of Useless Features: Is it Molecular Noise Suppression?, The American Naturalist 111, no.977977 (Oct 2015): 123–133.https://doi.org/10.1086/283143Brian K. Suarez Neandertal dental asymmetry and the probable mutation effect, American Journal of Physical Anthropology 41, no.33 (Nov 1974): 411–416.https://doi.org/10.1002/ajpa.1330410307D.L. Greene Dental anthropology of early Egypt and Nubia, Journal of Human Evolution 1, no.33 (May 1972): 315–324.https://doi.org/10.1016/0047-2484(72)90067-XMilford H. Wolpoff The effect of mutations under conditions of reduced selection, Social Biology 16, no.11 (Aug 2010): 11–23.https://doi.org/10.1080/19485565.1969.9987795Ralph L. Holloway Structural reduction through the "probable mutation effect". A critique with questions regarding human evolution, American Journal of Physical Anthropology 25, no.11 (Jul 1966): 7–11.https://doi.org/10.1002/ajpa.1330250103
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