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The Effects of Changes in Chromosome Number on Amphibian Development

1945; University of Chicago Press; Volume: 20; Issue: 1 Linguagem: Inglês

10.1086/394703

1539-7718

G. Fankhauser,

Insect and Arachnid Ecology and Behavior

Previous articleNext article No AccessThe Effects of Changes in Chromosome Number on Amphibian DevelopmentG. FankhauserG. Fankhauser Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The Quarterly Review of Biology Volume 20, Number 1Mar., 1945 Published in association with Stony Brook University Article DOIhttps://doi.org/10.1086/394703 Views: 35Total views on this site Citations: 253Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Hannah F. Fung, Dominique C. Bergmann Function follows form: How cell size is harnessed for developmental decisions, European Journal of Cell Biology 102, no.22 (Jun 2023): 151312.https://doi.org/10.1016/j.ejcb.2023.151312Jamie Davies, Michael Levin Synthetic morphology with agential materials, Nature Reviews Bioengineering 1, no.11 (Jan 2023): 46–59.https://doi.org/10.1038/s44222-022-00001-9Root Gorelick An Odd Pediocactus knowltonii, Cactus and Succulent Journal 95, no.11 (Jan 2023).https://doi.org/10.2985/015.095.0112Wesley P Clawson, Michael Levin Endless forms most beautiful 2.0: teleonomy and the bioengineering of chimaeric and synthetic organisms, Biological Journal of the Linnean Society 8 (Jul 2022).https://doi.org/10.1093/biolinnean/blac073Michael W. Itgen, Giovanna R. Natalie, Dustin S. Siegel, Stanley K. Sessions, Rachel Lockridge Mueller Genome size drives morphological evolution in organ‐specific ways, Evolution 21 (Jun 2022).https://doi.org/10.1111/evo.14519Vasilios Nanos, Michael Levin Multi-scale Chimerism: An experimental window on the algorithms of anatomical control, Cells & Development 169 (Mar 2022): 203764.https://doi.org/10.1016/j.cdev.2021.203764James P. Bogart Gynogenetic diploids, tetraploids, or octoploids, and a path to polyploidy in anuran amphibians, Genome 64, no.1212 (Dec 2021): 1053–1065.https://doi.org/10.1139/gen-2021-0019Christopher D. Small, James P. Davis, Bryan D. Crawford, Tillmann J. Benfey Early, nonlethal ploidy and genome size quantification using confocal microscopy in zebrafish embryos, Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 336, no.66 (Jul 2021): 496–510.https://doi.org/10.1002/jez.b.23069Manuel Alejandro Otero, Pablo Raúl Grenat, Clarisa Lourdes Bionda, Mariana Baraquet, Favio Ezequiel Pollo, Nancy Edith Salas, Adolfo Ludovico Martino Age and growth in an anuran hybrid zone: Fitness-related traits of the diploid/polyploid ground frog complex (genus Odontophrynus) from central Argentina, Zoologischer Anzeiger 293 (Jul 2021): 257–262.https://doi.org/10.1016/j.jcz.2021.07.001Douglas S. Glazier Genome Size Covaries More Positively with Propagule Size than Adult Size: New Insights into an Old Problem, Biology 10, no.44 (Mar 2021): 270.https://doi.org/10.3390/biology10040270Adam Hermaniuk, Iris L. E. van de Pol, Wilco C. E. P. Verberk Are acute and acclimated thermal effects on metabolic rate modulated by cell size? A comparison between diploid and triploid zebrafish larvae, The Journal of Experimental Biology 224, no.11 (Nov 2020): jeb227124.https://doi.org/10.1242/jeb.227124Wallace F. Marshall Scaling of Subcellular Structures, Annual Review of Cell and Developmental Biology 36, no.11 (Oct 2020): 219–236.https://doi.org/10.1146/annurev-cellbio-020520-113246Chase C. Wesley, Sampada Mishra, Daniel L. Levy Organelle size scaling over embryonic development, WIREs Developmental Biology 9, no.55 (Jan 2020).https://doi.org/10.1002/wdev.376Michael Levin The Biophysics of Regenerative Repair Suggests New Perspectives on Biological Causation, BioEssays 42, no.22 (Jan 2020): 1900146.https://doi.org/10.1002/bies.201900146Joseph F. Hoffman Reflections on the crooked timber of red blood cell physiology, Blood Cells, Molecules, and Diseases 79 (Nov 2019): 102354.https://doi.org/10.1016/j.bcmd.2019.102354Kelley Leung, Louis Zande, Leo W. Beukeboom Life‐history traits of the Whiting polyploid line of the parasitoid Nasonia vitripennis, Entomologia Experimentalis et Applicata 167, no.77 (Jul 2019): 655–669.https://doi.org/10.1111/eea.12808Manuel A. Otero, Julián A. Valetti, Clarisa L. Bionda, Nancy E. Salas, Adolfo L. Martino Are ploidy and age size-related? A comparative study on tetraploid Pleurodema kriegi and octoploid P. cordobae (Anura: Leptodactylidae) from Central Argentina, Zoologischer Anzeiger 268 (May 2017): 136–142.https://doi.org/10.1016/j.jcz.2016.07.005Maurine Neiman, Margaret J. Beaton, Dag O. Hessen, Punidan D. Jeyasingh, Lawrence J. Weider Endopolyploidy as a potential driver of animal ecology and evolution, Biological Reviews 92, no.11 (Oct 2015): 234–247.https://doi.org/10.1111/brv.12226Tanvir-Ul-Hassan Dar, Reiaz-Ul Rehman Significance of Polyploidy, (Nov 2017): 53–68.https://doi.org/10.1007/978-81-322-3772-3_5Jing Wang, Qingfeng Liu, Kaikun Luo, Xuan Chen, Jun Xiao, Chun Zhang, Min Tao, Rurong Zhao, Shaojun Liu Cell fusion as the formation mechanism of unreduced gametes in the gynogenetic diploid hybrid fish, Scientific Reports 6, no.11 (Aug 2016).https://doi.org/10.1038/srep31658Adam Hermaniuk, Mariusz Rybacki, and Jan R. E. Taylor Low Temperature and Polyploidy Result in Larger Cell and Body Size in an Ectothermic Vertebrate, Physiological and Biochemical Zoology 89, no.22 (Jan 2016): 118–129.https://doi.org/10.1086/684974C.J. Rothfels, S.P. Otto Polyploid Speciation, (Jan 2016): 317–326.https://doi.org/10.1016/B978-0-12-800049-6.00073-1Lidija D. Vuković, Predrag Jevtić, Lisa J. Edens, Daniel L. Levy New Insights into Mechanisms and Functions of Nuclear Size Regulation, (Jan 2016): 1–59.https://doi.org/10.1016/bs.ircmb.2015.11.001Álvaro S. Roco, Allen W. Olmstead, Sigmund J. Degitz, Tosikazu Amano, Lyle B. Zimmerman, Mónica Bullejos Coexistence of Y, W, and Z sex chromosomes in Xenopus tropicalis, Proceedings of the National Academy of Sciences 112, no.3434 (Jul 2015).https://doi.org/10.1073/pnas.1505291112Audrey Barranger, Abdellah Benabdelmouna, Lionel Dégremont, Thierry Burgeot, Farida Akcha Parental exposure to environmental concentrations of diuron leads to aneuploidy in embryos of the Pacific oyster, as evidenced by fluorescent in situ hybridization, Aquatic Toxicology 159 (Feb 2015): 36–43.https://doi.org/10.1016/j.aquatox.2014.11.011Root Gorelick Do Micrognathozoa have micro-genomes?, Biological Journal of the Linnean Society 112, no.33 (Apr 2014): 640–644.https://doi.org/10.1111/bij.12284Satu Kujawski, Weilin Lin, Florian Kitte, Mandy Börmel, Steffen Fuchs, Guruchandar Arulmozhivarman, Sebastian Vogt, Denise Theil, Yixin Zhang, Christopher L. Antos Calcineurin Regulates Coordinated Outgrowth of Zebrafish Regenerating Fins, Developmental Cell 28, no.55 (Mar 2014): 573–587.https://doi.org/10.1016/j.devcel.2014.01.019Predrag Jevtić, Daniel L. Levy Mechanisms of Nuclear Size Regulation in Model Systems and Cancer, (Jan 2014): 537–569.https://doi.org/10.1007/978-1-4899-8032-8_25Su Kyoung Kim, Na Young Shim, Won Young Lee, Min Seop Choi, Eun Hee Choi, Hyun Jeong Lim Morphological and physiological comparison between triploid and diploid Pacific Oyster, Crassostrea gigas, The Korean Journal of Malacology 29, no.33 (Sep 2013): 217–223.https://doi.org/10.9710/kjm.2013.29.3.217Adam Hermaniuk, Nicolas B. M. Pruvost, Piotr Kierzkowski, Maria Ogielska Genetic and Cytogenetic Characteristics of Pentaploidy in Water Frogs, Herpetologica 69, no.11 (Mar 2013): 36–45.https://doi.org/10.1655/HERPETOLOGICA-D-12-00037M Neiman, A D Kay, A C Krist Can resource costs of polyploidy provide an advantage to sex?, Heredity 110, no.22 (Nov 2012): 152–159.https://doi.org/10.1038/hdy.2012.78Jamie A. Davies Growth, Proliferation and Death, (Jan 2013): 283–305.https://doi.org/10.1016/B978-0-12-391062-2.00022-XMaurine Neiman, Adam D. Kay, Amy C. Krist SENSITIVITY TO PHOSPHORUS LIMITATION INCREASES WITH PLOIDY LEVEL IN A NEW ZEALAND SNAIL, Evolution (Jan 2013): no–no.https://doi.org/10.1111/evo.12026Daniel L. Levy, Rebecca Heald Mechanisms of Intracellular Scaling, Annual Review of Cell and Developmental Biology 28, no.11 (Nov 2012): 113–135.https://doi.org/10.1146/annurev-cellbio-092910-154158B. K. Mable, M. A. Alexandrou, M. I. Taylor Genome duplication in amphibians and fish: an extended synthesis, Journal of Zoology 284, no.33 (Jun 2011): 151–182.https://doi.org/10.1111/j.1469-7998.2011.00829.xJulian C. Lui, Jeffrey Baron Mechanisms Limiting Body Growth in Mammals, Endocrine Reviews 32, no.33 (Mar 2011): 422–440.https://doi.org/10.1210/er.2011-0001Yee-Hung M. Chan, Wallace F. Marshall Scaling properties of cell and organelle size, Organogenesis 6, no.22 (Oct 2014): 88–96.https://doi.org/10.4161/org.6.2.11464C. Niehrs On growth and form: a Cartesian coordinate system of Wnt and BMP signaling specifies bilaterian body axes, Development 137, no.66 (Feb 2010): 845–857.https://doi.org/10.1242/dev.039651Ali Ferjani, Gorou Horiguchi, Hirokazu Tsukaya Organ size control in Arabidopsis: Insights from compensation studies, PLANT MORPHOLOGY 22, no.11 (Jan 2010): 65–71.https://doi.org/10.5685/plmorphol.22.65Richard Gordon Google Embryo for Building Quantitative Understanding of an Embryo As It Builds Itself. II. Progress Toward an Embryo Surface Microscope, Biological Theory 4, no.44 (Apr 2015): 396–412.https://doi.org/10.1162/BIOT_a_00010Francesc Piferrer, Andy Beaumont, Jean-Claude Falguière, Martin Flajšhans, Pierrick Haffray, Lorenzo Colombo Polyploid fish and shellfish: Production, biology and applications to aquaculture for performance improvement and genetic containment, Aquaculture 293, no.3-43-4 (Aug 2009): 125–156.https://doi.org/10.1016/j.aquaculture.2009.04.036Michael A. Crickmore, Richard S. Mann The control of size in animals: insights from selector genes, BioEssays 30, no.99 (Sep 2008): 843–853.https://doi.org/10.1002/bies.20806RG Edwards The significance of parthenogenetic virgin mothers in bonnethead sharks and mice, Reproductive BioMedicine Online 15, no.11 (Jan 2007): 12–15.https://doi.org/10.1016/S1472-6483(10)60684-0Shuji Ishihara, Kunihiko Kaneko Turing pattern with proportion preservation, Journal of Theoretical Biology 238, no.33 (Feb 2006): 683–693.https://doi.org/10.1016/j.jtbi.2005.06.016Ichiro Tazawa, Hitoshi Okumoto, Akihiko Kashiwagi Skin Pigmentary Variants in Rana Nigromaculata, Journal of Clinical Biochemistry and Nutrition 38, no.33 (Jan 2006): 195–203.https://doi.org/10.3164/jcbn.38.195T. RYAN GREGORY, BARBARA K. MABLE Polyploidy in Animals, (Jan 2005): 427–517.https://doi.org/10.1016/B978-012301463-4/50010-3N Gong, H Yang, G Zhang, B J Landau, X Guo Chromosome inheritance in triploid Pacific oyster Crassostrea gigas Thunberg, Heredity 93, no.55 (Jul 2004): 408–415.https://doi.org/10.1038/sj.hdy.6800517Bangyan Stiles, Matthias Groszer, Shunyou Wang, Jing Jiao, Hong Wu PTENless means more, Developmental Biology 273, no.22 (Sep 2004): 175–184.https://doi.org/10.1016/j.ydbio.2004.06.008J Adam Luckenbach, John Godwin, Harry V Daniels, Jessica M Beasley, Craig V Sullivan, Russell J Borski Induction of diploid gynogenesis in southern flounder (Paralichthys lethostigma) with homologous and heterologous sperm, Aquaculture 237, no.1-41-4 (Aug 2004): 499–516.https://doi.org/10.1016/j.aquaculture.2004.05.005B. K. MABLE ‘Why polyploidy is rarer in animals than in plants’: myths and mechanisms, Biological Journal of the Linnean Society 82, no.44 (Aug 2004): 453–466.https://doi.org/10.1111/j.1095-8312.2004.00332.xC Luo, B Li Diploid-dependent regulation of gene expression: a genetic cause of abnormal development in fish haploid embryos, Heredity 90, no.55 (Apr 2003): 405–409.https://doi.org/10.1038/sj.hdy.6800263Myriam Morelli Effects of heat-shock on cell division and microtubule organization in zygotes of the shrimp Penaeus indicus (Crustacea, Decapoda) observed with confocal microscopy, Aquaculture 216, no.1-41-4 (Feb 2003): 39–53.https://doi.org/10.1016/S0044-8486(01)00894-8Isabel T. Mercadal de Barrio, Alfonso Barrio, Tetraploidía en Ceratophrys (Anura, Leptodactylidae), análisis del registro fósil, Iheringia. Série Zoologia 92, no.33 (Sep 2002): 17–31.https://doi.org/10.1590/S0073-47212002000300003Zhaoping Wang, Ximing Guo, Standish K Allen, Rucai Wang Heterozygosity and body size in triploid Pacific oysters, Crassostrea gigas Thunberg, produced from meiosis II inhibition and tetraploids, Aquaculture 204, no.3-43-4 (Feb 2002): 337–348.https://doi.org/10.1016/S0044-8486(01)00845-6R.T. Prehn The epigenetic instruction manual for the operation of the genome, Medical Hypotheses 58, no.22 (Feb 2002): 177–181.https://doi.org/10.1054/mehy.2001.1510Robert L. Davis, David L. Turner, Louise M. Evans, Marc W. Kirschner Molecular Targets of Vertebrate Segmentation, Developmental Cell 1, no.44 (Oct 2001): 553–565.https://doi.org/10.1016/S1534-5807(01)00054-5C Potter Mechanisms of size control, Current Opinion in Genetics & Development 11, no.33 (Jun 2001): 279–286.https://doi.org/10.1016/S0959-437X(00)00191-XD. Schmeller, A. Crivelli, M. Veith Is triploidy indisputably determinable in hybridogenetic hybrids by planimetric analyses of erythrocytes?, Zoosystematics and Evolution 77, no.11 (Apr 2008): 71–77.https://doi.org/10.1002/mmnz.20010770112D. Schmeller, A. Crivelli, M. Veith Is triploidy indisputably determinable in hybridogenetic hybrids by planimetric analyses of erythrocytes?, Mitteilungen aus dem Museum für Naturkunde in Berlin. Zoologische Reihe 77, no.11 (Jan 2001): 71–77.https://doi.org/10.1002/mmnz.4850770112Richard H. Gomer Not being the wrong size, Nature Reviews Molecular Cell Biology 2, no.11 (Jan 2001): 48–55.https://doi.org/10.1038/35048058M�nica Alonso, Yara A. Tabata, Marcos G. Rigolino, Ricardo Y. Tsukamoto Effect of induced triploidy on fin regeneration of juvenile rainbow trout,Oncorhynchus mykiss, Journal of Experimental Zoology 287, no.77 (Jan 2000): 493–502.https://doi.org/10.1002/1097-010X(20001201)287:7<493::AID-JEZ5>3.0.CO;2-8Sarah P Otto, Jeannette Whitton Polyploid Incidence and Evolution, Annual Review of Genetics 34, no.11 (Dec 2000): 401–437.https://doi.org/10.1146/annurev.genet.34.1.401Jacques Montagne Genetic and Molecular Mechanisms of Cell Size Control, Molecular Cell Biology Research Communications 4, no.44 (Oct 2000): 195–202.https://doi.org/10.1006/mcbr.2001.0284S.J. Day, P.A. Lawrence Measuring dimensions: the regulation of size and shape, Development 127, no.1414 (Jul 2000): 2977–2987.https://doi.org/10.1242/dev.127.14.2977Anthony J. Flemming, Zai-Zhong Shen, Ana Cunha, Scott W. Emmons, Armand M. Leroi Somatic polyploidization and cellular proliferation drive body size evolution in nematodes, Proceedings of the National Academy of Sciences 97, no.1010 (May 2000): 5285–5290.https://doi.org/10.1073/pnas.97.10.5285Kim J. Dale, Olivier Pourquié A clock-work somite, BioEssays 22, no.11 (Jan 2000): 72–83.https://doi.org/10.1002/(SICI)1521-1878(200001)22:1<72::AID-BIES12>3.0.CO;2-SJ. M. Greeff, M. G. Storhas, N. K. Michiels Reducing losses to offspring mortality by redistributing resources, Functional Ecology 13, no.66 (Apr 2002): 786–792.https://doi.org/10.1046/j.1365-2435.1999.00370.xZhaoping Wang, Ximing Guo, Standish K Allen, Rucai Wang Aneuploid Pacific oyster (Crassostrea gigas Thunberg) as incidentals from triploid production, Aquaculture 173, no.1-41-4 (Mar 1999): 347–357.https://doi.org/10.1016/S0044-8486(98)00457-8S. Ohta, M. Sumida, M. Nishioka Sex-determining mechanism inBuergeria buergeri (Anura, Rhacophoridae). III. Does the ZZW triploid frog become female or male?, Journal of Experimental Zoology 283, no.33 (Feb 1999): 295–306.https://doi.org/10.1002/(SICI)1097-010X(19990215)283:3<295::AID-JEZ7>3.0.CO;2-QOlivier Pourquié 3 Segmentation of the Paraxial Mesoderm and Vertebrate Somitogenesis, (Jan 1999): 81–105.https://doi.org/10.1016/S0070-2153(08)60722-XH-S Yang, Y-Y Ting, H-C Chen Blocking polar body with cytochalasin B in the fertilized eggs of the small abalone, Haliotis diversicolor supertexta (Lischke), and the development and ploidy of the resultant embryos, Aquaculture Research 29, no.1111 (Jun 2008): 775–783.https://doi.org/10.1111/j.1365-2109.1998.tb01103.xTin Tin Su, Patrick H O'Farrell Size control: Cell proliferation does not equal growth, Current Biology 8, no.1919 (Sep 1998): R687–R689.https://doi.org/10.1016/S0960-9822(98)70436-1A. V. Suresh, R. J. Sheehan Muscle fibre growth dynamics in diploid and triploid rainbow trout, Journal of Fish Biology 52, no.33 (Apr 2005): 570–587.https://doi.org/10.1111/j.1095-8649.1998.tb02018.xV. Suresh, R. J. Sheehan Biochemical and morphological correlates of growth in diploid and triploid rainbow trout, Journal of Fish Biology 52, no.33 (Apr 2005): 588–599.https://doi.org/10.1111/j.1095-8649.1998.tb02019.xXiming Guo, Gregory A. DeBrosse, Standish K. Allen All-triploid Pacific oysters (Crassostrea gigas Thunberg) produced by mating tetraploids and diploids, Aquaculture 142, no.3-43-4 (Jun 1996): 149–161.https://doi.org/10.1016/0044-8486(95)01243-5X. Guo and S. K. Allen Jr. Reproductive Potential and Genetics of Triploid Pacific Oysters, Crassostrea gigas (Thunberg), The Biological Bulletin 187, no.33 (Sep 2016): 309–318.https://doi.org/10.2307/1542288K. Varadaraj Production of viable haploidOreochromis mossambicus gynogens using UV-irradiated sperm, Journal of Experimental Zoology 267, no.44 (Nov 1993): 460–467.https://doi.org/10.1002/jez.1402670412Martin Flajšhans, Pavel Kvasnička, Petr Ráb Genetic studies in tench (Tinca tinca L.): high incidence of spontaneous triploidy, Aquaculture 110, no.3-43-4 (Mar 1993): 243–248.https://doi.org/10.1016/0044-8486(93)90372-6X. Guo, K. Cooper, W. K. Hershberger, and K. K. Chew Genetic Consequences of Blocking Polar Body I with Cytochalasin B in Fertilized Eggs of the Pacific Oyster, Crassostrea gigas: I. Ploidy of Resultant Embryos, The Biological Bulletin 183, no.33 (Sep 2016): 381–386.https://doi.org/10.2307/1542013C.C. Henery, J.B.L. Bard, M.H. Kaufman Tetraploidy in mice, embryonic cell number, and the grain of the developmental map, Developmental Biology 152, no.22 (Aug 1992): 233–241.https://doi.org/10.1016/0012-1606(92)90131-YC. C. Henery, M. H. Kaufman Relationship between cell size and nuclear volume in nucleated red blood cells of developmentally matched diploid and tetraploid mouse embryos, Journal of Experimental Zoology 261, no.44 (Apr 1992): 472–478.https://doi.org/10.1002/jez.1402610414David G. Sperry Lumbar lateral motor columns and hindlimbs of twoXenopus laevis chromosome mosaics, American Journal of Anatomy 191, no.44 (Aug 1991): 391–400.https://doi.org/10.1002/aja.1001910406L. A. Lowcock, R. W. Murphy Pentaploidy in hybrid salamanders demonstrates enhanced tolerance of multiple chromosome sets, Experientia 47, no.55 (May 1991): 490–493.https://doi.org/10.1007/BF01959952Lawrence E. Licht, Leslie A. Lowcock Genome size and metabolic rate in salamanders, Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 100, no.11 (Jan 1991): 83–92.https://doi.org/10.1016/0305-0491(91)90089-VEmanuel D. Pollack, Helen M. Maheras-Rarick Differential limb regeneration in diploid and triploidRana pipiens larvae with reference to spinal motor neuron development, Journal of Experimental Zoology 254, no.33 (Jun 1990): 276–285.https://doi.org/10.1002/jez.1402540306Lawrence E Licht, James P Bogart Comparative rates of oxygen consumption and water loss in diploid and polyploid salamanders (genus ambystoma), Comparative Biochemistry and Physiology Part A: Physiology 97, no.44 (Jan 1990): 569–572.https://doi.org/10.1016/0300-9629(90)90129-GJames P. Bogart, Richard P. Elinson, Lawrence E. Licht Temperature and Sperm Incorporation in Polyploid Salamanders, Science 246, no.49334933 (Nov 1989): 1032–1034.https://doi.org/10.1126/science.2587986K Varadaraj, T J Pandian Induction of allotriploids in the hybrids ofOreochromis mossambicus female × red tilapia male, Proceedings: Animal Sciences 98, no.55 (Sep 1989): 351–358.https://doi.org/10.1007/BF03179961David G. Sperry Lumbar lateral motor column development in triploidXenopus laevis, The Journal of Comparative Neurology 278, no.33 (Dec 1988): 446–452.https://doi.org/10.1002/cne.902780312David G. Sperry Effects of increasing ploidy on the lumbar lateral motor column and hindlimb of newly metamorphosedXenopus laevis: A comparison of diploid and triploid siblings, The Journal of Comparative Neurology 277, no.44 (Nov 1988): 499–508.https://doi.org/10.1002/cne.902770404S. G. Vassetzky Meiotic Divisions, (Jan 1988): 279–339.https://doi.org/10.1007/978-1-4684-0682-5_4Ben G. Szaro, Robert Tompkins, Ben G. Szaro Effect of tetraploidy on dendritic branching in neurons and glial cells of the frog,Xenopus laevis, The Journal of Comparative Neurology 258, no.22 (Apr 1987): 304–316.https://doi.org/10.1002/cne.902580210Gary H. Thorgaard Ploidy manipulation and performance, Aquaculture 57, no.1-41-4 (Oct 1986): 57–64.https://doi.org/10.1016/0044-8486(86)90180-8Eeva Therman Numerically Abnormal Chromosome Constitutions in Humans, (Jan 1986): 194–210.https://doi.org/10.1007/978-1-4684-0269-8_21Julian Lewis Programs of cell division in the lateral line system, Trends in Neurosciences 9 (Jan 1986): 135–138.https://doi.org/10.1016/0166-2236(86)90043-3S. Chaudhry, M. Vohra An Incidence of Endopolyploidy in the Polytene Chromosomes of a Mosquito Anopheles Culicifacies (Culicidae: Diptera), Caryologia 39, no.22 (Jan 1986): 161–164.https://doi.org/10.1080/00087114.1986.10797777B S Hiremath, M S Chennaveeraiah Cytological studies inSonchus oleraceous Linn., Proceedings / Indian Academy of Sciences 95, no.66 (Dec 1985).https://doi.org/10.1007/BF03053675Robb F Leary, Fred W Allendorf, Kathy L Knudsen, Gary H Thorgaard Heterozygosity and developmental stability in gynogenetic diploid and triploid rainbow trout, Heredity 54, no.22 (Apr 1985): 219–225.https://doi.org/10.1038/hdy.1985.29S Kamel, J.E Marsden, F.H Pough Diploid and tetraploid grey treefrogs (Hyla chrysoscelis and Hyla versicolor) have similar metabolic rates, Comparative Biochemistry and Physiology Part A: Physiology 82, no.11 (Jan 1985): 217–220.https://doi.org/10.1016/0300-9629(85)90729-7JEAN BRACHET NUCLEOCYTOPLASMIC INTERACTIONS IN OOCYTES AND EGGS, (Jan 1985): 73–287.https://doi.org/10.1016/B978-0-12-123371-6.50007-3Christian Cayrol, Andr� Jaylet, Vincent Ferrier, Fran�ois Gasser A genetic study of various enzyme polymorphisms in Pleurodeles waltlii (Urodele, Amphibian). III. The relationship between sex-linked peptidase-1 expression and gene-dose effects, Biochemical Genetics 21, no.5-65-6 (Jun 1983): 551–559.https://doi.org/10.1007/BF00484446C.E. Purdom Genetic engineering by the manipulation of chromosomes, Aquaculture 33, no.1-41-4 (Jun 1983): 287–300.https://doi.org/10.1016/0044-8486(83)90409-XMichael A. Goldman, Philip T. LoVerde, C. Larry Chrisman HYBRID ORIGIN OF POLYPLOIDY IN FRESHWATER SNAILS OF THE GENUS BULINUS (MOLLUSCA: PLANORBIDAE), Evolution 37, no.33 (May 2017): 592–600.https://doi.org/10.1111/j.1558-5646.1983.tb05576.xM. L. Beck, C. J. Biggers Erythrocyte measurements of diploid and triploid Ctenopharyngodon idella x Hypophthalmichthys nobilis hybrids, Journal of Fish Biology 22, no.44 (Apr 1983): 497–502.https://doi.org/10.1111/j.1095-8649.1983.tb04770.xC. Larry Chrisman, William R. Wolters, George S. Libey TRIPLOIDY IN CHANNEL CATFISH, Journal of the World Mariculture Society 14, no.1-41-4 (Mar 2009): 279–293.https://doi.org/10.1111/j.1749-7345.1983.tb00084.xJay E. Mittenthal, Robert M. Mazo A model for shape generation by strain and cell-cell adhesion in the epithelium of an arthropod leg segment, Journal of Theoretical Biology 100, no.33 (Feb 1983): 443–483.https://doi.org/10.1016/0022-5193(83)90441-1R.F. Lincoln, A.P. Scott Production of all-female triploid rainbow trout, Aquaculture 30, no.1-41-4 (Jan 1983): 375–380.https://doi.org/10.1016/0044-8486(83)90179-5Charlotte J Barker, Melvin L Beck, Charles J Biggers Hematologic and enzymatic analysis of Ctenopharyngodon idella × Hypophthalmichthys nobilis F1 hybrids, Comparative Biochemistry and Physiology Part A: Physiology 74, no.44 (Jan 1983): 915–918.https://doi.org/10.1016/0300-9629(83)90368-7Gary H. Thorgaard 8 Chromosome Set Manipulation and Sex Control in Fish, (Jan 1983): 405–434.https://doi.org/10.1016/S1546-5098(08)60308-8K. Ueno, B. Arimoto Induction of triploids inRhodeus ocellatus ocellatus by cold shock treatment of fertilized eggs, Experientia 38, no.55 (May 1982): 544–546.https://doi.org/10.1007/BF02327041R. F. Lincoln Sexual maturation in triploid male plaice (Pleuronectes platessa) and plaice x flounder (Platichthys flesus) hybrids, Journal of Fish Biology 19, no.44 (Oct 1981): 415–426.https://doi.org/10.1111/j.1095-8649.1981.tb05845.xRobert G. McKinnell, Betsy T. Kren, Robert Bergad, Melissa Schultheis, Timothy Byrne, J. W. Schaad Dominant lethality in Xenopus laevis induced with triethylenemelamine (TEM), Teratogenesis, Carcinogenesis, and Mutagenesis 1, no.33 (Jan 1981): 283–294.https://doi.org/10.1002/tcm.1770010305Donna M. Cassidy, Antonie W. Blackler Induction of triploidy inXenopus laevis by heat shocking of the egg before and after fertilization, Journal of Experimental Zoology 211, no.33 (Mar 1980): 379–385.https://doi.org/10.1002/jez.1402110315James P. Bogart Evolutionary Implications of Polyploidy in Amphibians and Reptiles, (Jan 1980): 341–378.https://doi.org/10.1007/978-1-4613-3069-1_18Eeva Therman Numerically Abnormal Chromosome Constitutions in Man, (Jan 1980): 136–149.https://doi.org/10.1007/978-1-4684-0107-3_14S. Subtelny Migration and Replication of the Germ Cell Line in Rana pipiens, (Jan 1980): 157–165.https://doi.org/10.1007/978-3-540-38267-6_21Arun Kumar Sharma, Archana Sharma Staining, (Jan 1980): 91–139.https://doi.org/10.1016/B978-0-408-70942-2.50010-9J. C. Gerhart Mechanisms Regulating Pattern Formation in the Amphibian Egg and Early Embryo, (Jan 1980): 133–316.https://doi.org/10.1007/978-1-4684-9933-9_4Dana C. Reinschmidt, Stuart J. Simon, E. Peter Volpe, Robert Tompkins Production of tetraploid and homozygous diploid amphibians by suppression of first cleavage, Journal of Experimental Zoology 210, no.11 (Oct 1979): 137–143.https://doi.org/10.1002/jez.1402100115Mark S. Ellinger Ontogeny of melanophore patterns in haploid and diploid embryos of the frog,Bombina orientalis, Journal of Morphology 162, no.11 (Oct 1979): 77–91.https://doi.org/10.1002/jmor.1051620106Leszek Berger Egg Size as an Index of Phenotype In Progeny OfRana esculenta Females, Mitteilungen aus dem Museum für Naturkunde in Berlin. Zoologisches Museum und Institut für Spezielle Zoologie 〈Berlin〉 55, no.11 (Jul 1979): 187–202.https://doi.org/10.1002/mmnz.4830550117J.R. Gold Cytogenetics, (Jan 1979): 353–405.https://doi.org/10.1016/S1546-5098(08)60030-8Marcus Jacobson, Giro Hirose Origin of the Retina from Both Sides of the Embryonic Brain: A Contribution to the Problem of Crossing at the Optic Chiasma, Science 202, no.43684368 (Nov 1978): 637–639.https://doi.org/10.1126/science.705349V. Ferrier, A. Jaylet Induction of triploidy in the newt Pleurodeles waltlii by heat shock or hydrostatic pressure, Chromosoma 69, no.11 (Jan 1978): 47–63.https://doi.org/10.1007/BF00327380Emanuel D. Pollack, Judi Koves Compensatory responses in the development of the brachial lateral motor column in triploidRana pipiens, The Anatomical Record 188, no.22 (Jun 1977): 173–179.https://doi.org/10.1002/ar.1091880204G.W. Salisbury, R.G. Hart, J.R. Lodge The spermatozoan genome and fertility, American Journal of Obstetrics and Gynecology 128, no.33 (Jun 1977): 342–350.https://doi.org/10.1016/0002-9378(77)90635-4F. Harvey Pough Acid Precipitation and Embryonic Mortality of Spotted Salamanders, Ambystoma maculatum, Science 192, no.42344234 (Apr 1976): 68–70.https://doi.org/10.1126/science.3852F. Fontana Nuclear DNA Content and Cytometry of Erythrocytes of Huso Huso L., Acipenser Sturio L. and Acipenser Naccarii Bonaparte, Caryologia 29, no.11 (Jan 1976): 127–138.https://doi.org/10.1080/00087114.1976.10796655R. J. Valenti Induced polyploidy in Tilapia aurea (Steindachner) by means of temperature shock treatment, Journal of Fish Biology 7, no.44 (Jul 1975): 519–528.https://doi.org/10.1111/j.1095-8649.1975.tb04627.xPamela Jones, H. Jackson, M. H. S. Whiting Parthenogenic development after chemical treatment ofXenopus laevis spermatozoa, Journal of Experimental Zoology 192, no.11 (Apr 1975): 73–81.https://doi.org/10.1002/jez.1401920109K.C. Carter, D.P. Fox Locust embryos mosaic for haploid and diploid cells, Developmental Biology 42, no.22 (Feb 1975): 388–390.https://doi.org/10.1016/0012-1606(75)90342-5Pierre Deparis, Jean-Claude Beetschen, André Jaylet Red blood cells and hemoglobin concentration in normal diploid and several types of polyploid salamanders, Comparative Biochemistry and Physiology Part A: Physiology 50, no.22 (Feb 1975): 263–266.https://doi.org/10.1016/0300-9629(75)90009-2G. M. Malacinski, A. J. Brothers Mutant Genes in the Mexican Axolotl, Science 184, no.41424142 (Jun 1974): 1142–1147.https://doi.org/10.1126/science.184.4142.1142Jane E. Brown, K. W. Jones Basic Concepts of Differentiation and Growth of Cells, (Jan 1974): 1–51.https://doi.org/10.1007/978-1-4899-3304-1_1Erik Niebuhr Triploidy in man, Human Genetics 21, no.22 (Jan 1974): 103–125.https://doi.org/10.1007/BF00281030Michael C. Cimino The nuclear DNA content of diploid and triploid Poeciliopsis and other poeciliid fishes with reference to the evolution of unisexual forms, Chromosoma 47, no.33 (Jan 1974): 297–307.https://doi.org/10.1007/BF00328863R.