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Fungi contribute to ecosystem function through nutrient cycling and decomposition but may be affected by major disturbances such as fire. Some ecosystems are fire-adapted, such as prairies which require cyclical burning to mitigate woody plant encroachment and reduce litter. While fire suppresses fire-sensitive fungi, pyrophilous fungi may continue providing ecosystem functions. Using litter bags, we measured the litter decomposition at three prairies with unburned and burned sections, and we used Illumina sequencing to examine litter communities. We hypothesized that (H1) decomposition would be higher at unburned sites than burned, (H2) increased decomposition at unburned sites would be correlated with higher overall saprotroph diversity, with a lower diversity in autoclaved samples, and (H3) pyrophilous fungal diversity would be higher at burned sites and overall higher in autoclaved samples. H1 was not supported; decomposition was unaffected by burn treatments. H2 and H3 were somewhat supported; saprotroph diversity was lowest in autoclaved litter at burned sites, but pyrophilous fungal diversity was the highest. Pyrophilous fungal diversity significantly contributed to litter decomposition rates, while saprotroph diversity did not. Our findings indicate that fire-adapted prairies host a suite of pyrophilous saprotrophic fungi, and that these fungi play a primary role in litter decomposition post-fire when other fire-sensitive fungal saprotrophs are less abundant. 

Data include soil and litter measurements for moisture, pH, and carbon-to-nitrogen ratio. Samples were collected from 8 different ecoregions, as determined by NEON, at various NEON/LTER and/or other experimental sites. Soil cores and litter samples were taken in the spring and fall of 2022. 

Abstract PremiseUnderstanding how population dynamics vary in space and time is critical for understanding the basic life history and conservation needs of a species, especially for narrow endemic species whose populations are often in similar environments and therefore at increased risk of extinction under climate change. Here, we investigated the spatial and temporal variation in population dynamics ofRanunculus austro‐oreganus, a perennial buttercup endemic to fragmented prairie habitat in one county in southern Oregon. MethodsWe performed demographic surveys of three populations ofR. austro‐oreganusover 4 years (2015–2018). We used size‐structured population models and life table response experiments to investigate vital rates driving spatiotemporal variation in population growth. ResultsOverall,R. austro‐oreganushad positive or stable stochastic population growth rates, though individual vital rates and overall population growth varied substantially among sites and years. All populations had their greatest growth in the same year, suggesting potential synchrony associated with climate conditions. Differences in survival contributed most to spatial variation in population growth, while differences in reproduction contributed most to temporal variation in population growth. ConclusionsPopulations of this extremely narrow endemic appear stable, with positive growth during our study window. These results suggest that populations ofR. austro‐oreganusare able to persist if their habitat is not eliminated by land‐use change. Nonetheless, its narrow distribution and synchronous population dynamics suggest the need for continued monitoring, particularly with ongoing habitat loss and climate change. 

The Ordway-Swisher Biological Station (OSBS) is a 38-km2 reserve owned by the University of Florida and is part of the National Ecological Observatory Network (NEON). The reserve contains several iconic Florida habitats, such as sandhill, mesic hammock, and scrubby flatwoods. While plants and animals have been extensively studied at OSBS, the fungi remain poorly known. Fungal inventories are critical to increase knowledge of both fungal diversity and species ranges, and thus to provide foundational data for a wide array of applications in ecology and resource management. Here, we present the results of a nine-year effort to collect, preserve, and DNA barcode the macrofungi at OSBS. This effort generated >1200 vouchered specimens and 984 ITS rDNA sequences, representing more than 546 species. Our sampling was dominated by Basidiomycota and revealed a high diversity of symbiotic ectomycorrhizal fungi, particularly species of Amanita, Cortinarius, and Russula. Sampling curves and both Chao1 and Jacknife1 richness estimators suggest that our DNA barcoding efforts captured only about half of the macrofungi species and that a more complete inventory would detect 897–1177 macrofungi species at OSBS. Our sampling found more species of macrofungi at OSBS than the known number of vertebrate animal species at the reserve and our estimates also suggest that there are likely more macrofungi species than plant species at OSBS. This study is the first comprehensive macrofungi inventory within a NEON site and highlights the importance of long-term monitoring to provide novel data on fungal diversity, community structure, conservation, biogeography, and taxonomy. 

IntroductionLogging impacts millions of hectares of forests globally every year, and not only affects tree cover, but also disrupts below-ground soil communities that are essential for forest ecosystems. Soil fungi are particularly vulnerable to such disturbances due to their reliance upon plant hosts as their source of carbon. Fluctuations within the major guilds of fungi important for forest function can have ramifications for plant communities and biogeochemical processes. We addressed questions about soil fungal communities in temperate forest stands with varying logging histories: (1) Do assembly patterns of soil fungal communities and functional guilds reflect historical differences in logging legacies? (2) Does sequencing of below-ground communities of fungi resemble the composition of surveys of fungal fruiting bodies? (3) How do fungal communities in the litter layer differ from those in the soil and do these assembly patterns change with logging history? MethodsOur study took place in the H. J. Andrews Experimental Forest in western Oregon, USA. We sampled soil and litter (Oi—Oe) in three sites with different logging histories: one clear cut in 1974, one selectively logged and thinned three times between 1974 and 2001, and one unlogged. We sequenced soil fungi separately for mineral soil samples and litter samples. Additionally, we compiled fruiting-body studies from 1972 through the present to compare with our eDNA samples. ResultsWe found that four decades after logging had ceased there were detectable signatures within the soil fungal communities that distinguished logged from unlogged sites, indicating a legacy that affects many generations of fungi (PERMANOVA;p< 0.001 for both soil and litter fungi). There were also significant differences between litter and mineral soil communities (PERMANOVA;p< 0.001) with higher relative abundances of pathogens within the litter layer and a greater proportion of mycorrhizal fungi in the soil. DiscussionThese results highlight the importance of including forest litter in studies, as entire guilds of fungi can be underestimated when considering a single fraction. Together, these results have repercussions for the regeneration of forests following logging, as the composition of fungal guilds important to plant functions do not fully recover even after decades of cessation.