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Abstract Abstract. Climate change is dramatically altering global precipitation patterns across terrestrial ecosystems, making it critically important that we understand both how and why plant species vary in their drought sensitivities. Andropogon gerardii and Schizachyrium scoparium, both C4 grasses, provide a model system for understanding the physiological mechanisms that determine how species of a single functional type can differ in drought responses, an issue remains a critical gap in our ability to model and predict the impacts of drought on grassland ecosystems. Despite its greater lability of foliar water content, previous experiments have demonstrated that S. scoparium maintains higher photosynthetic capacity during droughts. It is therefore likely that the ability of S. scoparium to withstand drought instead derives from a greater metabolic resistance to drought. Here, we tested the following hypotheses: (H1) A. gerardii is more vulnerable to drought than S. scoparium at both the population and organismal levels, (H2) A. gerardii is less stomatally flexible than S. scoparium, and (H3) A. gerardii is more metabolically limited than S. scoparium. Our results indicate that it is actually stomatal limitations of CO2 supply that limit A. gerardii photosynthesis during drought. Schizachyrium scoparium was more drought-resistant than A. gerardii based on long-term field data, organismal biomass production and physiological gas exchange measurements. While both S. scoparium and A. gerardii avoided metabolic limitation of photosynthesis, CO2 supply of A. gerardii was greatly reduced during late-stage drought stress. That two common, co-occurring C4 species possess such different responses to drought highlights the physiological variability inherent within plant functional groups and underscores the need for more studies of C4 drought tolerance. 

Soil moisture reductions during drought often inhibit soil microbial activity and inhibit decomposition rates by reducing microbial biomass or by altering microbial communities. Evidence suggests that soil water must drop below a critical threshold to inhibit microbial activity. Thus, it is likely that the seasonal timing of drought will determine the extent to which belowground processes are adversely impacted by drought. Specifically, the effects of drought might be minimal during cool, wet periods typical of late spring but dramatic during hot summer months with high evapotranspiration rates that lower soil moisture levels below the critical threshold. Here, we present results from a study designed to quantify the effect of drought on soil microbial abundance, community composition, and soil water diffusion across four months, and to then assess how drought impacts the microbial decomposition of leaf matter. We imposed a season‐long drought in a Wisconsin tallgrass prairie and measured soil moisture, bacterial composition and abundance, microbial respiration, and decomposition rates throughout the growing season. Bacterial communities varied considerably among dates, but drought did not affect either bacterial abundance or community composition. Microbial respiration declined significantly during periods of drought when soil pores likely became hydrologically isolated, ultimately reducing cumulative microbial respiration by 10%. The reduction in microbial activity in drought treatments caused a 50% decline in the decomposition of refractory material. Our study highlights that sublethal effects of drought on microbial communities, occurring only when soil moisture declined below a tolerance threshold, can have large impacts on microbial carbon release or decomposition, highlighting the need to incorporate such measures into future studies. 

ABSTRACT Microbial communities can be structured by both deterministic and stochastic processes, but the relative importance of these processes remains unknown. The ambiguity partly arises from an inability to disentangle soil microbial processes from confounding factors, such as aboveground plant communities or anthropogenic disturbance. In this study, we characterized the relative contributions of determinism and stochasticity to assembly processes of soil bacterial communities across a large environmental gradient of undisturbed Antarctic soils. We hypothesized that harsh soils would impose a strong environmental selection on microbial communities, whereas communities in benign soils would be structured largely by dispersal. Contrary to our expectations, dispersal was the dominant assembly mechanism across the entire soil environmental gradient, including benign environments. The microbial community composition reflects slowly changing soil conditions and dispersal limitation of isolated sites. Thus, stochastic processes, as opposed to deterministic, are primary drivers of soil ecosystem assembly across space at our study site. This is especially surprising given the strong environmental constraints on soil microorganisms in one of the harshest environments on the planet, suggesting that dispersal could be a driving force in microbial community assembly in soils worldwide. IMPORTANCE Because of their diversity and ubiquity, microbes provide an excellent means to tease apart how natural communities are structured. In general, ecologists believe that stochastic assembly processes, like random drift and dispersal, should dominate in benign environments while deterministic processes, like environmental filtering, should be prevalent in harsh environments. To help resolve this debate, we analyzed microbial community composition in pristine Antarctic soils devoid of human influence or plant communities for eons. Our results demonstrate that dispersal limitation is a surprisingly potent force of community limitation throughout all soil conditions. Thus, dispersal appears to be a driving force of microbial community assembly, even in the harshest of conditions. 

Yeast prions are self-perpetuating misfolded proteins that are infectious. In yeast, [PSI+] is the prion form of the Sup35 protein. While the study of [PSI+] has revealed important cellular mechanisms that contribute to prion propagation, the underlying cellular factors that influence prion formation are not well understood. Prion formation has been described as a multi-step process involving both the initial nucleation and growth of aggregates, followed by the subsequent transmission of prion particles to daughter cells. Prior evidence suggests that actin plays a role in this multi-step process, but actin’s precise role is unclear. Here, we investigate how actin influences the cell’s ability to manage newly formed visible aggregates and how actin influences the transmission of newly formed aggregates to future generations. At early steps, using 3D time-lapse microscopy, several actin mutants, and Markov modeling, we find that the movement of newly formed aggregates is random and actin independent. At later steps, our prion induction studies provide evidence that the transmission of newly formed prion particles to daughter cells is limited by the actin cytoskeletal network. We suspect that this limitation is because actin is used to possibly retain prion particles in the mother cell.