2018
DOI: 10.1093/femsec/fiy208
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Diversity of fungi and bacteria in species-rich grasslands increases with plant diversity in shoots but not in roots and soil

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Cited by 37 publications
(43 citation statements)
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“…Because litter decomposition is a highly dynamic process with constantly changing litter quality and strong successional changes in the community of microbial decomposers (Chomel et al 2014;Tlàskal et al 2016), it is not unexpected that diversity relationships may change as well. Other studies also did not find any correlation between plant diversity and soil microbial diversity (Chodak et al 2015;Navratilova et al 2019). Perhaps in our study, this could be related to the negative correlation between shrub diversity and global soil microbial activity ( Figure 2a).…”
Section: Shrub Community Diversity Effectscontrasting
confidence: 60%
“…Because litter decomposition is a highly dynamic process with constantly changing litter quality and strong successional changes in the community of microbial decomposers (Chomel et al 2014;Tlàskal et al 2016), it is not unexpected that diversity relationships may change as well. Other studies also did not find any correlation between plant diversity and soil microbial diversity (Chodak et al 2015;Navratilova et al 2019). Perhaps in our study, this could be related to the negative correlation between shrub diversity and global soil microbial activity ( Figure 2a).…”
Section: Shrub Community Diversity Effectscontrasting
confidence: 60%
“…In the present study, there was a 3% contribution from soil properties in explaining fungal and bacterial diversity. Recent article reported 2-4% contribution of soil properties in explaining variations of fungal and bacterial diversity in a species-rich grassland [48]. Greater contributions of plant attributes than soil properties in explaining soil microbial diversity were also reported by several empirical studies [6,46,49].…”
Section: Discussionmentioning
confidence: 89%
“…No reuse allowed without permission. (Caporaso et al, 2012) and nu-SSU-0817/nu-SSU-1196 (Borneman and Hartin, 2000) were used to amplify the bacterial 16S rRNA gene and the fungal 18S rRNA gene, respectively, as previously described (Zifcakova et al, 2016;Navrátilová et al, 2019). PCR products were purified and sequenced on an Illumina MiSeq platform in the Laboratory of Environmental Microbiology, Institute of Microbiology of the Czech Academy of Sciences.…”
Section: Data Collectionmentioning
confidence: 99%