1 What are sexes, and why are there sexes? |
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1 | (17) |
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3 | (6) |
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3 | (2) |
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5 | (4) |
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6 | (1) |
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1.1.2b The benefits of sex |
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6 | (3) |
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1.2 Mating types, sexes, and genders |
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9 | (6) |
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1.2.1 What uses are primary mating types? |
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11 | (2) |
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1.2.1a Inbreeding avoidance |
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11 | (1) |
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1.2.1b Sex-advantage enhancement |
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11 | (1) |
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1.2.1c Control over organelle transmission |
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12 | (1) |
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1.2.1d Developmental switch |
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12 | (1) |
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1.2.2 Frequency-dependent selection on mating types |
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13 | (1) |
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1.2.3 Sexes and sex-ratio selection |
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14 | (1) |
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1.3 Sex roles, sexual conflicts, and sexual selection |
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15 | (1) |
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1.4 Sex determination versus sex differentiation |
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16 | (2) |
2 The diversity of sexual cycles |
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18 | (19) |
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2.1 Sexual cycles among eukaryotes |
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18 | (18) |
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2.1.1 Haploid versus diploid phases |
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18 | (6) |
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2.1.1a Is diploidy better? |
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20 | (3) |
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2.1.1b What maintains haplo-diplontic cycles? |
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23 | (1) |
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2.1.2 (An)isogamy: from mating types to sexes |
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24 | (2) |
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2.1.3 Modes and timing of sex determination |
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26 | (2) |
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2.1.4 Haplo-genotypic sex determination (H-GSD) |
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28 | (1) |
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2.1.5 Diplo-genotypic sex determination (D-GSD) |
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28 | (1) |
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2.1.6 Epigenetic sex differentiation |
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29 | (5) |
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2.1.6a Simultaneous hermaphroditism |
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29 | (1) |
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2.1.6b Sequential hermaphroditism |
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30 | (1) |
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2.1.6c Environmental sex determination (ESD) |
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31 | (1) |
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2.1.6d Social sex determination |
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32 | (1) |
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32 | (1) |
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2.1.6f Parasite manipulation |
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33 | (1) |
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2.1.7 Self-incompatibility systems and induction types |
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34 | (1) |
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2.1.8 Evolutionary paths among sex-determination modes |
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34 | (2) |
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2.2 The eukaryote tree of sex |
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36 | (1) |
3 Molecular mechanisms of sex determination |
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37 | (41) |
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3.1 Gene regulatory networks |
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37 | (4) |
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3.1.1 Sex-determination cascades |
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37 | (1) |
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38 | (2) |
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3.1.2a Transcription factors |
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38 | (1) |
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3.1.2b Post-transcriptional regulation |
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39 | (1) |
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3.1.2c Hormones and pheromones |
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40 | (1) |
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3.1.3 Molecular mechanisms of transitions |
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40 | (1) |
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3.2 Haploid mating-type determination |
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41 | (10) |
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3.2.1 What genes are on MAT loci? |
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41 | (2) |
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43 | (6) |
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43 | (1) |
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43 | (1) |
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44 | (3) |
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47 | (1) |
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47 | (2) |
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3.2.3 Epigenetic mating-type determination |
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49 | (2) |
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3.2.3a Mating-type switching |
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49 | (1) |
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3.2.3b Self-compatibility |
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50 | (1) |
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3.3 Diploid sex determination |
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51 | (20) |
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3.3.1 Sex determination in angiosperms |
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51 | (5) |
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3.3.2 Sex determination in animals |
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56 | (10) |
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57 | (4) |
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3.3.2b Sex determination in vertebrates |
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61 | (3) |
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3.3.2c Sex determination in Ecdysozoa |
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64 | (2) |
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3.3.3 Molecular mechanisms of sex manipulation by parasites |
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66 | (5) |
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3.4 Self-incompatibility systems and induction types |
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71 | (7) |
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71 | (2) |
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3.4.1a SI systems in angiosperms |
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71 | (2) |
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3.4.1b SI systems in ascidians |
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73 | (1) |
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73 | (17) |
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3.4.2a Mating types in ciliates |
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74 | (2) |
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3.4.2b Induction types in oomycetes |
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76 | (2) |
4 The quantitative genetics of sex determination |
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78 | (11) |
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4.1 Sex as a threshold trait |
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78 | (1) |
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78 | (2) |
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4.3 Environmental variance and random effects |
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80 | (1) |
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81 | (1) |
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4.5 The classical dichotomous view: GSD versus ESD |
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82 | (1) |
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83 | (1) |
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4.7 Heritability of sex ratios |
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84 | (2) |
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86 | (1) |
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4.9 Response to selection |
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86 | (1) |
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87 | (2) |
5 The evolution of sex chromosomes |
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89 | (26) |
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90 | (7) |
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90 | (3) |
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5.1.2 Proximate mechanisms |
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93 | (2) |
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5.1.3 Neo-sex chromosomes |
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95 | (2) |
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5.1.4 Pseudo-autosomal regions |
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97 | (1) |
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5.2 Genomic consequences of recombination arrest |
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97 | (16) |
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5.2.1 U and V chromosomes |
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99 | (2) |
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5.2.2 Y and W chromosomes |
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101 | (7) |
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5.2.2a Evolutionary forces on Y and W |
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101 | (1) |
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5.2.2b Empirical evidence |
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101 | (2) |
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5.2.2c Fitness costs to the heterogametic sex |
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103 | (1) |
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5.2.2d Opposing the decay: gene conversion and X-Y recombination |
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104 | (1) |
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5.2.2e Accommodating the decay: dosage compensation |
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104 | (3) |
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5.2.2f Are Y and W chromosomes doomed to extinction? |
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107 | (1) |
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5.2.3 X and Z chromosomes |
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108 | (9) |
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5.2.3a Evolutionary forces on X and Z |
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108 | (3) |
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5.2.3b Empirical evidence |
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111 | (2) |
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5.3 Heterogeneity between lineages |
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113 | (2) |
6 Evolutionary correlates of sex-determination systems |
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115 | (18) |
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6.1 Sex determination and polyploidy |
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115 | (1) |
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6.2 Sex determination and parthenogenesis |
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116 | (1) |
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6.3 Sex determination and sex allocation |
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117 | (7) |
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6.3.1 Parental control and genetic conflicts over sex allocation |
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118 | (2) |
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6.3.2 Meiotic-drive sex chromosomes and sex-ratio distorters |
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120 | (4) |
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6.4 Sexual dimorphism and sexual selection |
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124 | (2) |
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6.4.1 Are sex chromosomes attractors for sexually selected traits? |
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124 | (1) |
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6.4.2 Is female heterogamety more conducive to flashy males? |
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125 | (1) |
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6.5 Sex determination and speciation |
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126 | (7) |
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127 | (3) |
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130 | (1) |
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130 | (1) |
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6.5.4 Pre-mating isolation |
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130 | (1) |
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6.5.5 Sex chromosome introgression in hybrid zones |
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131 | (1) |
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6.5.6 What about systems lacking differentiated sex chromosomes? |
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132 | (1) |
7 Transitions among sex-determination systems |
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133 | (18) |
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7.1 A diversity of transitions |
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133 | (1) |
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134 | (10) |
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134 | (1) |
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7.2.2 Fitness differences between sex phenotypes |
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135 | (2) |
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7.2.2a SA-driven transitions |
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135 | (1) |
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7.2.2b Mutation-load driven transitions |
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136 | (1) |
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7.2.3 Sex-ratio selection |
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137 | (7) |
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7.2.3a Shifting optimal sex ratios |
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137 | (1) |
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7.2.3b Environmentally driven transitions |
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138 | (1) |
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138 | (6) |
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7.3 Open questions on SD transitions |
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144 | (3) |
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7.3.1 Why do turnover rates differ between lineages? |
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144 | (1) |
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7.3.2 Are some SD systems more labile or some transitions more likely? |
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145 | (2) |
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7.3.3 Are some chromosome pairs particularly good at sex? |
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147 | (1) |
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7.4 Perspectives on SD transitions |
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147 | (4) |
Glossary |
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151 | (9) |
References |
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160 | (35) |
Taxonomic Index |
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195 | (10) |
Author Index |
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205 | (7) |
Subject Index |
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212 | |