Using network analysis to explore co-occurrence patterns in soil microbial communities
By A. Barberán, S. Bates, E. Casamayor, Noah Fierer. The ISME Journal, 2011
2,585 citations recorded by the source corpus.
Subfields: Ecology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/5e1f5263b0fa4eb99401d37f2fd1bb1457c7b385
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology
- Noah Fierer
- L. Philippot
- J. Schimel
- Brajesh Kumar Singh
- William Walters
- O. Broennimann
- Sean Schaeffer
- M. Strickland
In Molecular Biology
- Noah Fierer
- Rob Knight
- William Walters
- J. Schimel
- Antonio Gonzalez
- Josh D. Neufeld
- M. Strickland
- Q. Shen
Citations in the corpus
- Describe, understand and predict: why do we need networks in ecology? (2016, background): “…and quantification their complexity (Bascompte 2009) and could contribute to finally unlocking key questions such as community assembly (Montoya & Sole 2003; Barber an et al. 2012), coexistence (Allesina & Levine 2011; Ulrich et al. 2014) and the concept of trophic niches (Dehling et al. 2016).”
- Microbes as Engines of Ecosystem Function: When Does Community Structure Enhance Predictions of Ecosystem Processes? (2016, background): “…R 2 0.59) and microbial predictors (average adjusted R 2 0.38) relative to other systems, and metrics of community diversity were more strongly correlated with the environment ( n = 7, average adjusted R 2 0.24) and had lower added value (average adjusted R 2 0.06) than in other ecosystem types.”
- Cropping practices manipulate abundance patterns of root and soil microbiome members paving the way to smart farming (2018, background): “applied in soil microbial ecology to explore patterns of community assembly [35], visualize response patterns of different taxonomic groups to agronomic practices [36], and to identify individual microbiome members that”
- Comparative analysis of diversity and environmental niches of soil bacterial, archaeal, fungal and protist communities reveal niche divergences along environmental gradients in the Alps (2021, background): “For example, Ktedonobacteria (Chloroflexi) were identified in higher proportions as specialists, possibly reflecting their habitat preference for oligotrophic and extreme environments (Barberán et al., 2012; Lynch et al., 2012; Tebo et al., 2015), including high elevation alpine soils (Adamczyk et a”
- Biogeographic patterns of microbial association networks in paddy soil within Eastern China (2020, background): “Although the network hub is missing in many network studies (Barber�an et al., 2012; Faust et al., 2012; Deng et al., 2016; Ma et al., 2016; Shi et al., 2016), a number of network hubs in the fungal and diazotrophic networks, as well as the bacteria-fungi network, were identified (Tables 2 and S6).”
- Soil networks become more connected and take up more carbon as nature restoration progresses (2017, positive): “Tightening of the networks reflects stronger co-occurring patterns of variation in soil biota 26 .”
- Metagenomic and network analysis reveal wide distribution and co-occurrence of environmental antibiotic resistance genes (2015, background): “, 2003), proteins in metabolic pathways (Guimerà and Amaral, 2005), coexisting patterns among microbial taxa in soils (Barberán et al., 2012), activated sludge (Ju et al.”