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Buscot, F.

Publications and source records attributed to Buscot, F..

2 recordsLinked to original sources

Strong positive biodiversity-productivity relationships in a subtropical forest experiment

Forest ecosystems contribute substantially to global terrestrial primary productivity and climate regulation, but, in contrast to grasslands, experimental evidence for a positive biodiversity-productivity relationship in highly diverse forests is still lacking1. Here, we provide such evidence from a large forest biodiversity experiment with a novel design2 in subtropical China. Productivity (stand-level tree basal area, aboveground volume and carbon and their annual increment) increased linearly with the logarithm of tree species richness. Additive partitioning3 showed that increasing positive complementarity effects combined with weakening negative selection effects caused a strengthening of the relationship over time. In 2-species mixed stands, complementary effects increased with functional distance and selection effects with vertical crown dissimilarity between species. Understorey shrubs reduced stand-level tree productivity, but this effect of competition was attenuated by shrub species richness, indicating that a diverse understorey may facilitate overall ecosystem functioning. Identical biodiversity-productivity relationships were found in plots of different size, suggesting that extrapolation to larger scales is possible. Our results highlight the potential of multi-species afforestation strategies to simultaneously contribute to mitigation of climate change and biodiversity restoration.

ecology

Young Genes To The Front -- A Strategy For Future Resistance Against Powdery Mildew?

Nonhost resistance of a plant against a microbial pathogen can be the result of a long-lasting coevolutionary optimization of resource allocation in both host and pathogen. Although this has been suggested for years, coevolutionary aspects leading to nonhost resistance in plants are not fully understood yet. Instead, most studies focus on limited subsets of genes which are differentially expressed in infected plants to describe details of defense strategies and symptoms of diseases.\n\nHere, we exploit publicly available whole genome gene expression data and combine them with evolutionary characteristics of genes to uncover a mechanism of host-pathogen coevolution. Our results suggest that metabolic efficiency in gene regulation is a key aspect leading to nonhost resistance. In addition, we find that progressing host-pathogen coevolution is accompanied by subtle, but systematic overexpression of recently founded genes. In support of our plant-specific data, we observe similar effects in animal species.

evolutionary biology