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Ecology and Evolution|February 22, 2021
Pliant pathogens: Estimating viral spread when confronted with new vector, host, and environmental conditionsAnita Porath-Krause, Ryan Campbell, Lauren Shoemaker, et al.Global Change Biology|May 20, 2022
Realistic rates of nitrogen addition increase carbon flux rates but do not change soil carbon stocks in a temperate grasslandMegan E Wilcots, Katie M Schroeder, Lang C DeLancey, et al.Ecology|July 16, 2019
Effects of nutrient supply, herbivory, and host community on fungal endophyte diversityEric W Seabloom, Bradford Condon, Linda Kinkel, et al.Global Change Biology|March 14, 2025
Multiple Nutrient Additions Homogenize Multidimensional Plant Stoichiometry in a Meadow SteppeYang Peng, Jian-Xia Yang, Eric W Seabloom, et al.Ecology Letters|March 3, 2015
The community ecology of pathogens: coinfection, coexistence and community compositionEric W Seabloom, Elizabeth T Borer, Kevin Gross, et al.Molecular Ecology|May 22, 2009
Strong population structure characterizes weediness gene evolution in the invasive grass species Brachypodium distachyonErica G Bakker, Brooke Montgomery, Tracy Nguyen, et al.Global Change Biology|July 10, 2026
Prolonged Nutrient Enrichment Slows the Recovery of Biodiversity and Productivity After Its CessationMiao He, Kathryn E Barry, Elizabeth T Borer, et al.Frontiers in Microbiology|October 22, 2024
Plant community richness and foliar fungicides impact soil <i>Streptomyces</i> inhibition, resistance, and resource use phenotypesMatthew Michalska-Smith, Daniel C Schlatter, Nuttapon Pombubpa, et al.Frontiers in Plant Science|March 20, 2025
Foliar fungi-imposed costs to plant productivity moderate shifts in composition of the rhizosphere microbiomeBrett R Lane, Molly A Kuhs, Max M Zaret, et al.Plos One|January 22, 2021
Lessons from movement ecology for the return to work: Modeling contacts and the spread of COVID-19Allison K Shaw, Lauren A White, Matthew Michalska-Smith, et al.Pageof 16