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  1. null (Ed.)
    Abstract The rarity of rapid campaigns to characterize soils across scales limits opportunities to investigate variation in soil carbon stocks (SOC) storage simultaneously at large and small scales, with and without site-level replication. We used data from two complementary campaigns at 40 sites in the United States across the National Ecological Observatory Network (NEON), in which one campaign sampled profiles from closely co-located intensive plots and physically composited similar horizons, and the other sampled dozens of pedons across the landscape at each site. We demonstrate some consistencies between these distinct designs, while also revealing that within-site replication reveals patterns and predictors of SOC stocks not detectable with non-replicated designs. Both designs demonstrate that SOC stocks of whole soil profiles vary across continental-scale climate gradients. However, broad climate patterns may mask the importance of localized variation in soil physicochemical properties, as captured by within-site sampling, especially for SOC stocks of discrete genetic horizons. Within-site replication also reveals examples in which expectations based on readily explained continental-scale patterns do not hold. For example, even wide-ranging drainage class sequences within landscapes do not duplicate the clear differences in profile SOC stocks across drainage classes at the continental scale, and physicochemical factors associated with increasing B horizon SOC stocks at continental scales frequently do not follow the same patterns within landscapes. Because inferences from SOC studies are a product of their context (where, when, how), this study provides context—in terms of SOC stocks and the factors that influence them—for others assessing soils and the C cycle at NEON sites. 
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  2. null (Ed.)
    Abstract Variation in soil organic C (%OC) concentration has been associated with the concentration of reactive Fe- and Al-oxyhydroxide phases and exchangeable Ca, with the relative importance of these two stabilizing components shifting as soil pH moves from acid to alkaline. However, it is currently unknown if this pattern is similar or different with regard to measures of soil C persistence. We sampled soils from 3 horizons (uppermost A, uppermost B, C or lowest B horizons) across a pH gradient of 11 grass-dominated and 13 deciduous/mixed forest-dominated NEON sites to examine similarities and differences in the drivers of C concentration and persistence. Variation in C concentrations in all soils could be linked to abundances of Fe, Al and Ca, but were not significantly linked to variation in soil C persistence. Though pH was related to variation in Δ 14 OC, higher persistence was associated with more alkaline pH values. In forested soils, depth explained 75% of the variation in Δ 14 OC ( p  < 0.0001), with no significant additional correlations with extractable metal phases. In grasslands, soil organic C persistence was not associated with exchangeable Ca concentrations, but instead was explained by depth and inorganic C concentrations (R 2  = 0.76, p  < 0.0001), implying stabilization of organic C through association with carbonate precipitation. In grasslands, measures of substrate quality suggested greater persistence is also associated with a more advanced degree of decomposition. Results suggest that explanatory variables associated with C concentrations differ from those associated with persistence, and that reactive Fe- and Al-oxyhydroxide phases may not be present in high enough concentrations in most soils to offer any significant protective capacity. These results have significant implications for our understanding of how to model the soil C cycle and may suggest previously unrecognized stabilization mechanisms associated with carbonates and forms of extractable Si. 
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  3. null (Ed.)
    The highly infectious disease COVID-19 caused by the Betacoronavirus SARS-CoV-2 poses a severe threat to humanity, and demands for redirection of scientific efforts and criteria to organized research projects. The international Covid19-NMR consortium seeks to provide such new approaches by gathering scientific expertise worldwide. In particular, making available viral proteins and RNAs will pave the way to understanding the SARS-CoV-2 molecular components in detail. The research in Covid19-NMR and the resources provided through the consortium are fully disclosed to accelerate access and exploitation. NMR investigations of the viral molecular components are designated to provide the essential basis for further work, including macromolecular interaction studies and high-throughput drug screening. Here, we present the extensive catalogue of a holistic SARS-CoV-2 protein preparation approach based on the consortium’s collective efforts. We provide protocols for the large-scale production of more than 80% of all SARS-CoV-2 proteins or essential parts of them. Several of the proteins were produced in more than one laboratory, demonstrating the high interoperability between NMR groups worldwide. For the majority of proteins, we can produce isotope-labeled samples of HSQC-grade. Together with several NMR-chemical shift assignments made publicly available on covid19-nmr.com, we here provide highly valuable resources for the production of SARS-CoV-2 proteins in isotope labeled form. 
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