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  5. <title>UTas ePrints - Differential sex allocation in sand lizards: bright males induce daughter production in a species with heteromorphic sex chromosomes</title>
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  13. <meta content="Olsson, Mats" name="eprints.creators_name" />
  14. <meta content="Wapstra, Erik" name="eprints.creators_name" />
  15. <meta content="Uller, Tobias" name="eprints.creators_name" />
  16. <meta content="molsson@uow.edu.au" name="eprints.creators_id" />
  17. <meta content="erik.wapstra@utas.edu.au" name="eprints.creators_id" />
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  23. <meta content="Differential sex allocation
  24. in sand lizards: bright
  25. males induce daughter
  26. production in a species
  27. with heteromorphic sex
  28. chromosomes" name="eprints.title" />
  29. <meta content="pub" name="eprints.ispublished" />
  30. <meta content="270205" name="eprints.subjects" />
  31. <meta content="restricted" name="eprints.full_text_status" />
  32. <meta content="sex allocation; maternal allocation;
  33. male attractiveness;
  34. major histocompatibility complex;
  35. heteromorphic sex chromosomes
  36. " name="eprints.keywords" />
  37. <meta content="In sand lizards (Lacerta agilis), males with
  38. more and brighter nuptial coloration also have
  39. more DNA fragments visualized in restriction
  40. fragment length polymorphism analysis of their
  41. major histocompatibility complex class I loci
  42. (and, hence, are probably more heterozygous at
  43. these loci). Such males produce more viable
  44. offspring, with a particularly strong viability
  45. effect on daughters. This suggests that females
  46. should adjust both their reproductive investment
  47. and offspring sex ratio in relation to male
  48. coloration (i.e. differential allocation). Our
  49. results show that experimental manipulation of
  50. partner coloration in the wild results in signifi-
  51. cantly higher maternal effort and a 10% higher
  52. proportion of daughters than sons. This supports
  53. the hypothesis that females increase their
  54. maternal energetic expenditure and adjust their
  55. offspring sex ratio in response to high-quality
  56. partners. However, it also suggests that this has
  57. probably evolved through natural selection for
  58. increased offspring viability (primarily through
  59. production of daughters), rather than through
  60. increased mate attraction (e.g. sexy sons).
  61. " name="eprints.abstract" />
  62. <meta content="2005" name="eprints.date" />
  63. <meta content="published" name="eprints.date_type" />
  64. <meta content="Biology Letters" name="eprints.publication" />
  65. <meta content="1" name="eprints.volume" />
  66. <meta content="378-380" name="eprints.pagerange" />
  67. <meta content="10.1098/rsbl.2005.0327" name="eprints.id_number" />
  68. <meta content="TRUE" name="eprints.refereed" />
  69. <meta content="1744-9561" name="eprints.issn" />
  70. <meta content="http://dx.doi.org/10.1098/rsbl.2005.0327" name="eprints.official_url" />
  71. <meta content="Anderholm, S., Olsson, M., Wapstra, E. &amp; Ryberg, K. 2004
  72. Fit and fat from enlarged badges: a field experiment on
  73. male sand lizards. Proc. R. Soc. B 271(Suppl. 4),
  74. S142–S144. (doi:10.1098/rsbl.2003.0094.)
  75. Andersson, M. 1994 Sexual selection. Princeton University
  76. Press.
  77. Burley, N. 1981 Sex-ratio manipulation and selection for
  78. attractiveness. Science 211, 721–722.
  79. Burley, N. 1982 Facultative sex ratio manipulation. Am.
  80. Nat. 120, 81–107.
  81. Burley, N. 1986 Sex-ratio manipulation in color-banded
  82. populations of zebra finches. Evolution 40, 1191–1206.
  83. Charnov, E. 1982 The theory of sex allocation. Princeton
  84. University Press.
  85. Ellegren, H., Gustafsson, L. &amp; Sheldon, B. C. 1996 Sex
  86. ratio adjustment in relation to paternal attractiveness in
  87. a wild bird population. Proc. Natl Acad. Sci. USA 93,
  88. 11 723–11 728.
  89. Fedorka, K. M. &amp; Mousseau, T. A. 2004 Female mating
  90. bias results in conflicting sex-specific offspring fitness.
  91. Nature 429, 65–67.
  92. Grindstaff, J. L., Buerkle, C. A., Casto, J. M., Nolan Jr, V.
  93. &amp; Ketterson, E. D. 2001 Offspring sex ratio is unrelated
  94. to male attractiveness in dark-eyed juncos ( Junco hyemalis).
  95. Behav. Ecol. Sociobiol. 50, 312–316.
  96. Gullberg, A., Olsson, M. &amp; Tegelstro¨m, H. 1997 Male
  97. mating success, reproductive success and multiple paternity
  98. in a natural population of sand lizards: behavioural
  99. and molecular genetics data. Mol. Ecol. 6, 105–112.
  100. Hardy, I. C. W. 2002 Sex ratios: concepts and research
  101. methods. Cambridge University Press.
  102. Harlow, P. 1996 A harmless technique for sexing hatchling
  103. lizards. Herpetol. Rev. 27, 71–72.
  104. Olsson, M. &amp; Madsen, T. 2001 ‘Promiscuity’ in sand lizards
  105. and adder snakes: causes and consequences. J. Hered.
  106. 92, 190–197.
  107. Olsson, M., Gullberg, A. &amp; Tegelstro¨m, H. 1996 Mate
  108. guarding in male sand lizards (Lacerta agilis). Behaviour
  109. 133, 367–386.
  110. Olsson, M., Madsen, T., Nordby, J., Wapstra, E., Ujvari, B.
  111. &amp; Wittsell, H. 2003 Major histocompatibility complex
  112. and mate choice in sand lizards. Proc. R. Soc. B
  113. 270(Suppl. 2), S254–S256. (doi:10.1098/rsbl.2003.
  114. 0079.)
  115. Olsson, M., Ujvari, B., Madsen, T., Uller, T. &amp; Wapstra, E.
  116. 2004 Haldane rules: costs of outbreeding at production
  117. of daughters in sand lizards. Ecol Lett. 7, 924–928.
  118. Olsson, M., Madsen, T., Uller, T., Wapstra, E. &amp; Ujvari, B.
  119. 2005 The role of Haldane’s rule in sex allocation.
  120. Evolution 59, 221–225.
  121. Olsson, M., Madsen, T., Wapstra, E., Silverin, Ujvari, B. &amp;
  122. Wittzell, H. In press. MHC, health, color, and reproductive
  123. success in sand lizards. Behav. Ecol. Sociobiol.
  124. Saino, N., Ellegren, H. &amp; Møller, A. P. 1999 No evidence
  125. for adjustment of sex allocation in relation to paternal
  126. ornamentation and paternity in barn swallows. Mol. Ecol.
  127. 8, 399–406.
  128. Shaw, R. F. &amp; Mohler, J. D. 1953 The selective advantage
  129. of the sex ratio. Am. Nat. 87, 337–342.
  130. Sheldon, B. C., Andersson, S., Griffith, S. C., O¨
  131. rnborg, J.
  132. &amp; Sendencka, J. 1999 Ultraviolet colour variation influences
  133. blue tit sex ratio. Nature 402, 874–877.
  134. West, S. A. &amp; Sheldon, B. 2002 Constraints in the evolution
  135. of sex ratio adjustment. Science 295, 1685–1688.
  136.  
  137. " name="eprints.referencetext" />
  138. <meta content="Olsson, Mats and Wapstra, Erik and Uller, Tobias (2005) Differential sex allocation in sand lizards: bright males induce daughter production in a species with heteromorphic sex chromosomes. Biology Letters, 1 . pp. 378-380. ISSN 1744-9561" name="eprints.citation" />
  139. <meta content="http://eprints.utas.edu.au/2195/1/Differentialsexalloction.pdf" name="eprints.document_url" />
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  141. <meta content="Differential sex allocation
  142. in sand lizards: bright
  143. males induce daughter
  144. production in a species
  145. with heteromorphic sex
  146. chromosomes" name="DC.title" />
  147. <meta content="Olsson, Mats" name="DC.creator" />
  148. <meta content="Wapstra, Erik" name="DC.creator" />
  149. <meta content="Uller, Tobias" name="DC.creator" />
  150. <meta content="270205 Genetic Development (incl. Sex Determination)" name="DC.subject" />
  151. <meta content="In sand lizards (Lacerta agilis), males with
  152. more and brighter nuptial coloration also have
  153. more DNA fragments visualized in restriction
  154. fragment length polymorphism analysis of their
  155. major histocompatibility complex class I loci
  156. (and, hence, are probably more heterozygous at
  157. these loci). Such males produce more viable
  158. offspring, with a particularly strong viability
  159. effect on daughters. This suggests that females
  160. should adjust both their reproductive investment
  161. and offspring sex ratio in relation to male
  162. coloration (i.e. differential allocation). Our
  163. results show that experimental manipulation of
  164. partner coloration in the wild results in signifi-
  165. cantly higher maternal effort and a 10% higher
  166. proportion of daughters than sons. This supports
  167. the hypothesis that females increase their
  168. maternal energetic expenditure and adjust their
  169. offspring sex ratio in response to high-quality
  170. partners. However, it also suggests that this has
  171. probably evolved through natural selection for
  172. increased offspring viability (primarily through
  173. production of daughters), rather than through
  174. increased mate attraction (e.g. sexy sons).
  175. " name="DC.description" />
  176. <meta content="2005" name="DC.date" />
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  182. <meta content="Olsson, Mats and Wapstra, Erik and Uller, Tobias (2005) Differential sex allocation in sand lizards: bright males induce daughter production in a species with heteromorphic sex chromosomes. Biology Letters, 1 . pp. 378-380. ISSN 1744-9561" name="DC.identifier" />
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  287. <h1 class="ep_tm_pagetitle">Differential sex allocation in sand lizards: bright males induce daughter production in a species with heteromorphic sex chromosomes</h1>
  288. <p style="margin-bottom: 1em" class="not_ep_block"><span class="person_name">Olsson, Mats</span> and <span class="person_name">Wapstra, Erik</span> and <span class="person_name">Uller, Tobias</span> (2005) <xhtml:em>Differential sex allocation in sand lizards: bright males induce daughter production in a species with heteromorphic sex chromosomes.</xhtml:em> Biology Letters, 1 . pp. 378-380. ISSN 1744-9561</p><p style="margin-bottom: 1em" class="not_ep_block"></p><table style="margin-bottom: 1em" class="not_ep_block"><tr><td valign="top" style="text-align:center"><a href="http://eprints.utas.edu.au/2195/1/Differentialsexalloction.pdf"><img alt="[img]" src="http://eprints.utas.edu.au/style/images/fileicons/application_pdf.png" class="ep_doc_icon" border="0" /></a></td><td valign="top"><a href="http://eprints.utas.edu.au/2195/1/Differentialsexalloction.pdf"><span class="ep_document_citation">PDF</span></a> - Full text restricted - Requires a PDF viewer<br />80Kb</td><td><form method="get" accept-charset="utf-8" action="http://eprints.utas.edu.au/cgi/request_doc"><input accept-charset="utf-8" value="2779" name="docid" type="hidden" /><div class=""><input value="Request a copy" name="_action_null" class="ep_form_action_button" onclick="return EPJS_button_pushed( '_action_null' )" type="submit" /> </div></form></td></tr></table><p style="margin-bottom: 1em" class="not_ep_block">Official URL: <a href="http://dx.doi.org/10.1098/rsbl.2005.0327">http://dx.doi.org/10.1098/rsbl.2005.0327</a></p><div class="not_ep_block"><h2>Abstract</h2><p style="padding-bottom: 16px; text-align: left; margin: 1em auto 0em auto">In sand lizards (Lacerta agilis), males with&#13;
  289. more and brighter nuptial coloration also have&#13;
  290. more DNA fragments visualized in restriction&#13;
  291. fragment length polymorphism analysis of their&#13;
  292. major histocompatibility complex class I loci&#13;
  293. (and, hence, are probably more heterozygous at&#13;
  294. these loci). Such males produce more viable&#13;
  295. offspring, with a particularly strong viability&#13;
  296. effect on daughters. This suggests that females&#13;
  297. should adjust both their reproductive investment&#13;
  298. and offspring sex ratio in relation to male&#13;
  299. coloration (i.e. differential allocation). Our&#13;
  300. results show that experimental manipulation of&#13;
  301. partner coloration in the wild results in signifi-&#13;
  302. cantly higher maternal effort and a 10% higher&#13;
  303. proportion of daughters than sons. This supports&#13;
  304. the hypothesis that females increase their&#13;
  305. maternal energetic expenditure and adjust their&#13;
  306. offspring sex ratio in response to high-quality&#13;
  307. partners. However, it also suggests that this has&#13;
  308. probably evolved through natural selection for&#13;
  309. increased offspring viability (primarily through&#13;
  310. production of daughters), rather than through&#13;
  311. increased mate attraction (e.g. sexy sons).&#13;
  312. </p></div><table style="margin-bottom: 1em" cellpadding="3" class="not_ep_block" border="0"><tr><th valign="top" class="ep_row">Item Type:</th><td valign="top" class="ep_row">Article</td></tr><tr><th valign="top" class="ep_row">Keywords:</th><td valign="top" class="ep_row">sex allocation; maternal allocation;&#13;
  313. male attractiveness;&#13;
  314. major histocompatibility complex;&#13;
  315. heteromorphic sex chromosomes&#13;
  316. </td></tr><tr><th valign="top" class="ep_row">Subjects:</th><td valign="top" class="ep_row"><a href="http://eprints.utas.edu.au/view/subjects/270205.html">270000 Biological Sciences &gt; 270200 Genetics &gt; 270205 Genetic Development (incl. Sex Determination)</a></td></tr><tr><th valign="top" class="ep_row">ID Code:</th><td valign="top" class="ep_row">2195</td></tr><tr><th valign="top" class="ep_row">Deposited By:</th><td valign="top" class="ep_row"><span class="ep_name_citation"><span class="person_name">Dr Erik Wapstra</span></span></td></tr><tr><th valign="top" class="ep_row">Deposited On:</th><td valign="top" class="ep_row">15 Oct 2007 14:01</td></tr><tr><th valign="top" class="ep_row">Last Modified:</th><td valign="top" class="ep_row">09 Jan 2008 02:30</td></tr><tr><th valign="top" class="ep_row">ePrint Statistics:</th><td valign="top" class="ep_row"><a target="ePrintStats" href="/es/index.php?action=show_detail_eprint;id=2195;">View statistics for this ePrint</a></td></tr></table><p align="right">Repository Staff Only: <a href="http://eprints.utas.edu.au/cgi/users/home?screen=EPrint::View&amp;eprintid=2195">item control page</a></p>
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