Rhizosphere bacterial community composition in natural stands of Carex arenaria (sand sedge) is determined by bulk soil community composition

By Annelies S. de Ridder-Duine, G. Kowalchuk, P. Gunnewiek, W. Smant, J. A. Veen, W. Boer. 2005

193 citations recorded by the source corpus.

Subfields: Ecology

View Paper: https://www.semanticscholar.org/paper/e34bc181067b4f07c7d777fbc7623aa553d825e4

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In Ecology

Citations in the corpus

Continuous application of different organic additives can suppress tomato disease by inducing the healthy rhizospheric microbiota through alterations to the bulk soil microflora (2018, background): “Ridder-Duine et al. (2005) also demonstrated that the rhizosphere microbial composition of the wild plant C. arenaria was largely dependent on the microbial composition of the bulk soil.”
Impact of elevated carbon dioxide on the rhizosphere communities of Carex arenaria and Festuca rubra (2007, background): “…(Cyperaceae) is an established clonal perennial plant with long-lived tiller connections (rhizomes) (Tietema, 1981), commonly occurring on costal and inland sand dunes in Europe, and on the Atlantic coast of North and South America (Tietema, 1981; Olff et al., 2000; De Ridder-Duine et al., 2005).”
Microbe-mediated plant-soil feedback causes historical contingency effects in plant community assembly (2007, background): “…a selective effect on the organisms they accumulate in their rhizosphere (Kowalchuk et al. 2002), the abundance and composition of the soil community can be considered as the regional species pool that strongly affects the local community structure in the rhizosphere (De Ridder-Duine et al. 2005).”
Phosphorus uptake and rhizosphere properties of intercropped and monocropped maize, faba bean, and white lupin in acidic soil (2010, background): “According to De Ridder-Duine et al. (2005), the soil is more important than the plant.”
Predicting species distribution and abundance responses to climate change: why it is essential to include biotic interactions across trophic levels (2010, background): “Moreover, soil decomposer communities are supposed to be quite general in their decomposition activities and most soil organisms present in the rhizosphere originate from the soil surrounding the plant roots, rather than from further distance (de Ridder-Duine et al. 2005).”
Impact of root exudates and plant defense signaling on bacterial communities in the rhizosphere. A review (2011, background): “2.2 Plants affect their microbial rhizosphere community Soil is the main reservoir of the potential bacterial rhizosphere community (Normander and Prosser 2000; De Ridder-Duine et al. 2005; Berg and Smalla 2009).”
Microbial indicators for soil quality (2017, background): “For instance, when Carex arenaria, a non-mycorrhizal plant species, was grown in 10 different soils, the bacterial diversities in the respective rhizospheres were more similar to those of the bulk soil than to those of rhizosphere communities from other soils (De Ridder-Duine et al. 2005).”
Plant species and functional group effects on abiotic and microbial soil properties and plant–soil feedback responses in two grasslands (2006, result): “However, other studies have also shown that the effects of individual species on soil biota indeed can differ between soil types (e.g. Priha et al. 1999; Innes et al. 2004; De Ridder-Duine et al. 2005), and our results support the latter view.”
Effect of intercropping on crop yield and chemical and microbiological properties in rhizosphere of wheat (Triticum aestivum L.), maize (Zea mays L.), and faba bean (Vicia faba L.) (2007, background): “De Ridder-Duine et al. (2005) showed that the bacterial community in rhizosphere of Carex arenaria, grown in 10 different sites, had no consistent rhizosphere community across the sites, suggesting that the rhizosphere community composition was dominated by differences in soil properties.”