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When crossing pea plants, Mendel noticed that one of the parental traits would sometimes disappear in the first generation of offspring, called the F1 generation, and could reappear in the next generation (F2). He concluded that one of the traits must be dominant over the other, thereby causing masking of one trait in the F1 generation. When he crossed the F1 plants, he found that 75% of the offspring in the F2 generation had the dominant phenotype, while 25% had the recessive phenotype.
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While Mendel’s Law of Segregation states that the two alleles for one gene are separated into different gametes, a different question of how different genes are inherited remains. For example, is the gene for tall plants inherited with the gene for green peas? Mendel asked this question by experimenting with a dihybrid cross; a cross in which both parents are homozygous for two distinct traits resulting in an F1 generation that are heterozygous for both traits.
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Antagonistic coevolution between quantitative and Mendelian traits.

Masato Yamamichi1, Stephen P Ellner2

  • 1Hakubi Center for Advanced Research, Kyoto University, Sakyo, Kyoto 606-8501, Japan Center for Ecological Research, Kyoto University, Otsu, Shiga 520-2113, Japan Department of Ecology and Evolutionary Biology, Cornell University, Ithaca, NY 14853, USA yamamichi@ecology.kyoto-u.ac.jp.

Proceedings. Biological Sciences
|March 25, 2016
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Summary

Antagonistic coevolution between genetically asymmetric traits can lead to complex dynamics, including predator extinction. Understanding trait genetic architectures is key to predicting species interactions and biodiversity maintenance.

Keywords:
Red Queen dynamicscoevolutioneco-evolutionary feedbacksextinctionmajor-gene discrete traitpolygenic continuous trait

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Area of Science:

  • Evolutionary Biology
  • Ecology
  • Genetics

Background:

  • Coevolution is a major driver of biodiversity, historically studied for symmetric trait interactions.
  • Emerging evidence shows coevolution can involve genetically asymmetric traits, like quantitative and Mendelian traits.
  • Previous models often simplified trait interactions, potentially missing complex ecological outcomes.

Purpose of the Study:

  • To investigate the consequences of antagonistic coevolution between a quantitative predator trait and a Mendelian prey trait.
  • To explore the impact of phenotype matching on coevolutionary dynamics.
  • To analyze the role of eco-evolutionary dynamics in shaping population and evolutionary trajectories.

Main Methods:

  • Developed a two-dimensional model for trait coevolution incorporating phenotype matching.
  • Integrated eco-evolutionary dynamics to link trait evolution with population dynamics.
  • Analyzed bifurcations, bistability, and emergent dynamics like cycles and chaos.

Main Results:

  • Antagonistic coevolution between asymmetric traits resulted in complex bifurcations and bistability.
  • Eco-evolutionary dynamics revealed diverse outcomes: anti-phase cycles, in-phase cycles, chaotic dynamics, and predator extinction.
  • Predator extinction risk increased with complete prey trait dominance and rapid predator trait evolution.

Conclusions:

  • Recognizing the genetic architecture of interacting traits is crucial for understanding coevolution.
  • Asymmetric trait coevolution can generate complex population and evolutionary dynamics.
  • This study highlights the importance of integrating genetic details into ecological models to predict biodiversity outcomes.