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We used microbial lipid analysis to analyze microbial biomass and community structure during 6 years of experimental treatment at the Jasper Ridge Global Change Experiment ( JRGCE), a long-term multi-factor global change experiment in a California annual grassland. The microbial community fingerprint and specific biomarkers varied substantially from year to year, in both control and experimental treatment plots. Possible drivers of the variability included plant growth, soil moisture, and ambient temperature. Surprisingly, background variation in the microbial community was of a larger magnitude than even very significant treatment effects, and this variation appeared to constrain responses to treatment. Microbial communities were mostly not responsive or not consistently responsive to the experimental treatments. Both arbuscular mycorrhizal fungi biomarker abundance (16 : 1 ω5c) and the fungal to bacterial ratio were lower under nitrogen addition in most years. Bacterial lipid biomarker abundances (15 : 0 iso and 16 : 1 ω7c) were higher under nitrogen addition in 2002, the year of largest microbial biomass, suggesting that bacteria could respond more to nitrogen addition in years of better growth conditions. Nitrogen addition and warming led to an interactive effect on the Gram-positive bacterial biomarker and the fungal to bacterial ratio. These patterns indicate that in California grassland ecosystems, microbial communities may not respond substantially to future changes in climate and that nitrogen deposition may be a determinant of the soil response to global change. Further, year-to-year variation in microbial growth or community composition may be important determinants of ecosystem response to global change. [ABSTRACT FROM AUTHOR]

Soil microbiota play important and diverse roles in agricultural crop nutrition and productivity. Yet, despite increasing efforts to characterize soil bacterial and fungal assemblages, it is challenging to disentangle the influences of sampling design on assessments of communities. Here, we sought to determine whether composite samples—often analyzed as a low cost and effort alternative to replicated individual samples—provide representative summary estimates of microbial communities. At three Minnesota agricultural research sites planted with an oat cover crop, we conducted amplicon sequencing for soil bacterial and fungal communities (16SV4 and ITS2) of replicated individual or homogenized composite soil samples. We compared soil microbiota from within and among plots and then among agricultural sites using both sampling strategies. Results indicated that single or multiple replicated individual samples, or a composite sample from each plot, were sufficient for distinguishing broad site-level macroecological differences among bacterial and fungal communities. Analysis of a single sample per plot captured only a small fraction of the distinct OTUs, diversity, and compositional variability detected in the analysis of multiple individual samples or a single composite sample. Likewise, composite samples captured only a fraction of the diversity represented by the six individual samples from which they were formed, and, on average, analysis of two or three individual samples offered greater compositional coverage (i.e., greater number of OTUs) than a single composite sample. We conclude that sampling design significantly impacts estimates of bacterial and fungal communities even in homogeneously managed agricultural soils, and our findings indicate that while either strategy may be sufficient for broad macroecological investigations, composites may be a poor substitute for replicated samples at finer spatial scales. [ABSTRACT FROM AUTHOR]