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ZENODO
Dataset . 2022
License: CC BY
Data sources: Datacite
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
ZENODO
Dataset . 2022
License: CC BY
Data sources: Datacite
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
ZENODO
Dataset . 2022
License: CC BY
Data sources: ZENODO
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Growth rate and life history shape plant resistance.

Authors: Jacobsen, Deidra J.;

Growth rate and life history shape plant resistance.

Abstract

Premise: Plant defenses are shaped by many factors, including herbivory, lifespan, and mating system. Predictions about plant defense and resistance are often based on resource allocation trade‐offs with plant growth and reproduction. Additionally, two types of plant resistance, constitutive and induced resistance, are predicted to be evolutionary alternatives or redundant strategies. Given the variety of plant trait combinations and non‐mutually exclusive predictions, examining resistance strategies in related species with different combinations of growth and reproductive traits is important to tease apart roles of plant traits and evolutionary history on plant resistance. Methods: Phylogenetic comparative methods were used to examine the potentially interacting influences of life history (annual/perennial), mating system (self‐compatible/self-incompatible), and species growth rates on constitutive resistance and inducibility (additional resistance following damage) across Physalis species (Solanaceae). Results: Resistance was evolutionarily labile, and there was no correlation between constitutive resistance and inducibility. Annual species with fast growth rates displayed higher constitutive resistance, but growth rate did not affect constitutive resistance in perennials. In contrast, inducibility was negatively associated with species growth rate regardless of life history or mating system. Conclusions: The different effects of plant life history and growth rate on constitutive resistance and inducibility indicate that defensive evolution is unconstrained by a trade‐off between resistance types. The interactions among plant life history, growth, and herbivore resistance show that plant defense is shaped not only by herbivore environment, but also by plant traits that reflect a plant's evolutionary history and local selective pressures.

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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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