
The Evolution of Anisogamy: A Fundamental Phenomenon Underlying Sexual Selection
by Edited by Tatsuya Togashi , Paul Alan Cox-
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Summary
Author Biography
Table of Contents
List of contributors | p. x |
Introduction: The evolutionary mystery of gamete dimorphism | p. 1 |
The origin and maintenance of two sexes (anisogamy), and their gamete sizes by gamete competition | p. 17 |
Introduction | p. 17 |
The origin of anisogamy by disruptive selection on gamete size through gamete competition (PBS theory) | p. 18 |
Mating types and the PBS theory | p. 22 |
What determines whether the ESS is isogamy or anisogamy? | p. 29 |
The ancestral isogamous state-which came first, smaller or larger gametes? | p. 35 |
Requirements for PBS theory | p. 36 |
Evidence for PBS theory | p. 37 |
The loss of motility by female gametes (oogamy) | p. 40 |
Other theories for the origin of anisogamy and their relation to gamete competition | p. 41 |
Classical views | p. 42 |
Sperm limitation | p. 42 |
Conflicts with cytoplasmic elements | p. 43 |
Stability of anisogamy under internal fertilization why is anisogamy not lost when sperm competition is reduced? | p. 44 |
Sperm competition and a direct sperm size-number trade-off | p. 44 |
No sperm competition: sperm size trade off against mate acquisition or paternal care | p. 48 |
No sperm competition: sperm numbers increase fertility (sperm limitation) | p. 49 |
Summary of maintenance of anisogamy | p. 51 |
Optimal sizes of the male and female gametes: anisogamy ratios | p. 52 |
Gamete size dimorphism from PBS theory | p. 52 |
Optimization of ovum size | p. 54 |
Sperm competition and the evolution of sperm size | p. 54 |
Anisogamy as a stage in the evolutionary chain of sexuality | p. 68 |
The evolutionary instability of isogamy | p. 75 |
Introduction | p. 75 |
Sex-linked model when gamete size is determined independently in each mating type | p. 77 |
Non sex-linked model when gamete size is not associated with mating type | p. 83 |
Analyses of the sex-linked and non sex-linked models | p. 84 |
Cost of sex | p. 86 |
Simulation using an individual-based model | p. 87 |
Direct effects of size on gamete fitness | p. 88 |
Discussion | p. 90 |
Contact, not conflict, causes the evolution of anisogamy | p. 96 |
Introduction | p. 96 |
Model | p. 99 |
Hermaphroditic populations | p. 99 |
Synchronous spawners | p. 101 |
Genotype 11 | p. 101 |
Genotype 12 | p. 102 |
Frequency dependent collisions | p. 102 |
Condition for isogamy | p. 103 |
Condition for anisogamy | p. 104 |
Ecological predictions and tests | p. 107 |
Discussion | p. 108 |
Nucleo-cytoplasmic conflict and the evolution of gamete dimorphism | p. 111 |
Cytoplasmic selection may cause nucleo-cytoplasmic conflict | p. 111 |
The evolution of uniparental cytoplasmic inheritance and anisogamy driven by nucleo-cytoplasmic conflict | p. 112 |
Empirical evidence: uniparental inheritance | p. 115 |
Empirical evidence: selfish mitochondrial DNA | p. 116 |
Evaluation of the theoretical models and comparison of model predictions with empirical evidence | p. 117 |
The evolution of isogamous binary mating types | p. 118 |
The role of nucleo-cytoplasmic conflict in mating-type evolution | p. 119 |
Mating-type evolution as a consequence of selection for asymmetry in gamete recognition and adhesion | p. 120 |
Sexual fusion asymmetric from the start? | p. 120 |
Empirical evidence | p. 121 |
Mating types superimposed on male/female differentiation | p. 123 |
The origin of sexual asymmetry | p. 125 |
Adaptive significance of egg size variation of aquatic organisms in relation to mesoscale features of aquatic environments | p. 131 |
Introduction | p. 131 |
Turbulent disturbance and its influence on egg size and related traits | p. 134 |
An integrative view | p. 134 |
Observed patterns of egg size variation in fish species | p. 135 |
The model | p. 137 |
Floating versus demersal | p. 142 |
Optimal egg size and optimal parental care | p. 142 |
Optimal early life-stage traits | p. 144 |
Water turbulent disturbance as an explanatory factor of egg size and related traits | p. 146 |
Non-turbulent water movement and egg size | p. 147 |
Planktonic eggs and larvae in water currents | p. 147 |
The model | p. 150 |
Optimal egg size with no retention at the spawning site | p. 154 |
Optimal egg size and retention at the spawning site | p. 157 |
Ecological implications | p. 159 |
Female gamete size variation in aquatic environments | p. 161 |
Gamete encounters | p. 168 |
Introduction | p. 168 |
Occurrence of sperm limitation | p. 169 |
Unfertilized eggs | p. 169 |
Evolved features to avoid sperm limitation | p. 169 |
Laboratory observations | p. 170 |
Field surveys | p. 170 |
Mechanisms of encounter | p. 171 |
Gamete encounter rates | p. 171 |
Factors influencing encounter rates | p. 173 |
Predicted evolution of anisogamy | p. 176 |
Assumptions | p. 176 |
Selective pressures | p. 181 |
Consequences of more effective encounter mechanisms | p. 190 |
Questions for the future | p. 191 |
Evolution of anisogamy and related phenomena in marine green algae | p. 194 |
Introduction | p. 194 |
Uniparental inheritance of cytoplasmic genes and gamete size | p. 195 |
Gamete size and behavior | p. 196 |
Phototaxis and fertilization success | p. 198 |
Pheromonal male gamete attraction systems in external fertilizers | p. 200 |
Synchronous gamete production and release | p. 202 |
Reproductive investment, gamete size and number | p. 204 |
Gamete motility | p. 207 |
Sex ratio | p. 209 |
Dioecious versus monoecious life history | p. 211 |
Ferilization kinetics model | p. 211 |
Cost of sex | p. 216 |
Evolution of gamete size without mating types | p. 218 |
Fertilization kinetics and the evolution of anisogamy | p. 223 |
Parthenogenesis | p. 232 |
Currents and turbulence | p. 233 |
Tests of the PBS model | p. 233 |
Gamete survival | p. 235 |
Anisogamy and habitats | p. 236 |
Multicellularity | p. 236 |
Summary | p. 237 |
Index | p. 243 |
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