2023
DOI: 10.1016/j.apsoil.2022.104653
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Relationships between geochemical properties and microbial nutrient acquisition in tropical forest and cropland soils

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Cited by 10 publications
(6 citation statements)
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“…This natural difference in nutrient content between the soils from the north and south regions could influence the microbiome composition, according to the oligotrophic–copiotrophic theory [ 34 , 35 ]. This theory states that copiotrophic bacterial taxa (e.g., Proteobacteria and Firmicutes) usually are more prevalent in nutrient-rich conditions [ 34 , 36 , 37 ]; in contrast, oligotrophic bacteria (e.g., Acidobacteria, Gemmatimonadetes, Verrucomicrobia, and Chloroflexi) can maintain growth and be prevalent under nutrient-poor conditions [ 37 , 38 , 39 ]. We hypothesized that these differences in the soil nutrient content could be influencing partially the bacterial composition in the rhizosphere of the V. floribundum in Ecuador.…”
Section: Discussionmentioning
confidence: 99%
“…This natural difference in nutrient content between the soils from the north and south regions could influence the microbiome composition, according to the oligotrophic–copiotrophic theory [ 34 , 35 ]. This theory states that copiotrophic bacterial taxa (e.g., Proteobacteria and Firmicutes) usually are more prevalent in nutrient-rich conditions [ 34 , 36 , 37 ]; in contrast, oligotrophic bacteria (e.g., Acidobacteria, Gemmatimonadetes, Verrucomicrobia, and Chloroflexi) can maintain growth and be prevalent under nutrient-poor conditions [ 37 , 38 , 39 ]. We hypothesized that these differences in the soil nutrient content could be influencing partially the bacterial composition in the rhizosphere of the V. floribundum in Ecuador.…”
Section: Discussionmentioning
confidence: 99%
“…For instance, Henry and Swan (1974) determined from coarse woody debris (and standing trees) that forest structure in a temperate mixed hardwood forest was more driven by disturbance than autogenic succession. Development of nutrient limitations of microorganisms (e.g., Camenzind et al., 2018, Kidinda et al., 2023) can also be determined through nutrient and carbon responses of plants and litter‐SOM. Differing SOM responses to additional resources such as CO 2 in grasslands and forests (Terrer et al., 2021) and temperature in peatlands (Zeh et al., 2022) similarly can be clarified through plant resource economies, be it competition, growth form, litter production, or a combination thereof.…”
Section: Discussionmentioning
confidence: 99%
“…Soil aggregate stability (supervised by Nico Eisenhauer) will determine the resistance of soil aggregates against water as a disintegrating force. We will apply an approach modified from Kemper and Rosenau (1986). The resulting index represents the percentage of waterstable macroaggregates (> 250 μm).…”
Section: Methodsmentioning
confidence: 99%
“…They have studied the temporal and spatial drivers of soil communities and ecosystem functions across ecosystems (e.g. , Guerrero-Ramírez et al (2017), Craven et al (2018), Doetterl et al (2018), Gottschall et al (2019), Gottschall et al (2021, ), Kidinda et al (2023) and have linked soil communities to ecosystem functions (e.g. , , Beugnon et al (2021)).…”
Section: Preliminary Workmentioning
confidence: 99%