The following pages link to (Q3430416):
Displaying 34 items.
- Evolutionary and convergence stability for continuous phenotypes in finite populations derived from two-allele models (Q292785) (← links)
- Evolutionary dynamics of a quantitative trait in a finite asexual population (Q304470) (← links)
- Evolution of costly explicit memory and cumulative culture (Q327206) (← links)
- Mathematical models for immunology: current state of the art and future research directions (Q518216) (← links)
- The metapopulation fitness criterion: proof and perspectives (Q615598) (← links)
- The evolution of tuberculosis virulence (Q836209) (← links)
- The evolutionary dynamics of a population model with a strong Allee effect (Q888642) (← links)
- From the Price equation to the selection gradient in class-structured populations: a quasi-equilibrium route (Q1642531) (← links)
- Vegetation pattern formation in a fog-dependent ecosystem (Q1719983) (← links)
- A model for the evolutionary diversification of religions (Q1736301) (← links)
- Stochasticity, selection, and the evolution of cooperation in a two-level Moran model of the snowdrift game (Q1784295) (← links)
- The unavoidable costs and unexpected benefits of parasitism: population and metapopulation models of parasite-mediated competition (Q1788350) (← links)
- Song learning as an indicator mechanism: modelling the developmental stress hypothesis (Q1794350) (← links)
- What life cycle graphs can tell about the evolution of life histories (Q1937892) (← links)
- Check your assumptions: further scrutiny of basic model frameworks of antimicrobial resistance (Q2095397) (← links)
- Fractional order SIR epidemic model with Beddington-De Angelis incidence and Holling type II treatment rate for COVID-19 (Q2103107) (← links)
- Asymptotic of the largest Floquet multiplier for cooperative matrices (Q2103441) (← links)
- Fixation and effective size in a haploid-diploid population with asexual reproduction (Q2131420) (← links)
- The importance of chaotic attractors in modelling tumour growth (Q2150942) (← links)
- Fixation in the stochastic Lotka-Volterra model with small fitness trade-offs (Q2161379) (← links)
- Adaptive meiotic drive in selfing populations with heterozygote advantage (Q2169169) (← links)
- Density-dependent selection and the limits of relative fitness (Q2329323) (← links)
- Is there a Trivers-Willard effect for parental investment? Modelling evolutionarily stable strategies using a matrix population model with nonlinear mating (Q2337463) (← links)
- Evolution of stinginess and generosity in finite populations (Q2404006) (← links)
- Generation of variation and a modified mean fitness principle: necessity is the mother of genetic invention (Q2413530) (← links)
- The effect of dominance on polymorphism in Müllerian mimicry (Q2632187) (← links)
- The gossip paradox: why do bacteria share genes? (Q2686702) (← links)
- Coevolutionary dynamics of host immune and parasite virulence based on an age-structured epidemic model (Q2687734) (← links)
- Finding the boundary between evolutionary basins of attraction, and implications for Wright’s fitness landscape analogy (Q3301386) (← links)
- Life history and deleterious mutation rate coevolution (Q6078402) (← links)
- Evolutionary rescue via niche construction: infrequent construction can prevent post-invasion extinction (Q6090209) (← links)
- A simple model of nutrient recycling and dormancy in a chemostat: mathematical analysis and a second-order nonstandard finite difference method (Q6118875) (← links)
- Pulled, pushed or failed: the demographic impact of a gene drive can change the nature of its spatial spread (Q6171419) (← links)
- Infection-induced increases to population size during cycles in a discrete-time epidemic model (Q6494220) (← links)
