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‎404.html‎

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<li><a href="/publication/coblentz-2025/">Simple, universal rules predict trophic interaction strengths</a></li>
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<li><a href="/publication/li-2025-aa/">Body mass–biomass scaling modulates species keystone-ness to press perturbations</a></li>
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<li><a href="/publication/preston-2025-aa/">Age-prevalence curves in a multi-species parasite community</a></li>
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<li><a href="/publication/novak-2025-ab/">In defense of the original Type I functional response: The frequency and population-dynamic effects of feeding on multiple prey at a time</a></li>
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<li><a href="/publication/coblentz-2024/">Simple, universal rules predict trophic interaction strengths</a></li>
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<li><a href="/publication/novak-2024-aa/">Corrigendum: Geometric complexity and the information-theoretic comparison of functional-response models</a></li>
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<li><a href="/publication/novak-2023-aa/">High variation in handling times confers 35-year stability to predator feeding rates despite community change</a></li>

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<li><a href="https://novaklabosu.github.io/authors/kyle-coblentz/">Kyle Coblentz</a></li>
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<a href="/publication/novak-2025-ab/">In defense of the original Type I functional response: The frequency and population-dynamic effects of feeding on multiple prey at a time</a>
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<a href="/publication/coblentz-2025/">Simple, universal rules predict trophic interaction strengths</a>
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<a href="/publication/coblentz-2024/">Simple, universal rules predict trophic interaction strengths</a>
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<a href="/publication/li-2025-aa/">Body mass–biomass scaling modulates species keystone-ness to press perturbations</a>
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