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Rogers, D. A.

Publications and source records attributed to Rogers, D. A..

2 recordsLinked to original sources

Functional traits fail to predict long-term responses to climate change

AimEnvironmental conditions strongly affect the distribution and abundance of species via complex forces. Shifts in environmental conditions and differences in the speed and scale of these effects complicate our efforts to infer how species will respond to future environmental change. We test how 18 functional traits affect plant species responses to gradients in environmental conditions and 50-year shifts in climate. LocationWe analyzed 50-year shifts in the distribution and abundance of 153 plant species distributed across 284 sites in Wisconsin, USA. Time period1950s to 2000s. Major taxa studiedVascular plants (much of the flora of NE North America). MethodsWe used random forest and integrated hierarchical mixed models to test how plant abundances (and 50-year changes in abundance) track gradients in overstory, soil, and climatic conditions. ResultsWithin study periods, plant abundances reflect gradients in environmental conditions. Leaf traits affected local abundance (both directly and via trait-environment interactions) in the 1950s and 2000s. Strong soil and temperature effects in the 1950s have weakened while precipitation effects have strengthened. Although we expected these models to also predict how plants would respond to shifts in climate, they did not. Main conclusionsLags in species responses, increases in the stochastic forces affecting community assembly, and other forces limit the ability of models fitted to static data (e.g., space-for-time substitutions) to predict how plant species will respond to long-term shifts in environmental conditions. We must therefore be cautious about applying trait-based species distribution models to predict how climate change will affect species distributions and community structure.

ecology↗

AD Informer Set: Chemical tools to facilitate Alzheimer's disease drug discovery

IntroductionThe portfolio of novel targets to treat Alzheimers disease (AD) has been enriched by the AMP-AD program. MethodsA cheminformatics-driven effort enabled identification of existing small molecule modulators for many protein targets nominated by AMP-AD and suitable positive control compounds to be included in the set. ResultsWe have built an annotated set of 171 small molecule modulators, including mostly inhibitors, targeting 98 unique proteins that have been nominated by AMP-AD consortium members as novel targets for AD treatment. These small molecules vary in their quality and should be considered chemical tools that can be used in efforts to validate therapeutic hypotheses, but which would require further optimization. A physical copy of the AD Informer Set can be ordered via the AD Knowledge Portal. DiscussionSmall molecule tools that enable target validation are important tools for the translation of novel hypotheses into viable therapeutic strategies for AD.

neuroscience↗