2018
DOI: 10.1016/j.soilbio.2018.05.004
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Prokaryotic assemblages within permafrost active layer at Edmonson Point (Northern Victoria Land, Antarctica)

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Cited by 20 publications
(22 citation statements)
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“…Calibration curves with the standards 7-amino-4-methylcoumarin (MCA) or 4-methylumbelliferone (MUF) were performed for LAP or for β-GLU and AP, respectively. Results were elaborated and expressed as described in Papale et al [44] and references therein [45,46,47]. Cell-specific enzymatic activity was determined by normalizing the total (bulk) enzymatic activity to the prokaryotic cell abundance, taking into account the initial dilution of the brine samples.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Calibration curves with the standards 7-amino-4-methylcoumarin (MCA) or 4-methylumbelliferone (MUF) were performed for LAP or for β-GLU and AP, respectively. Results were elaborated and expressed as described in Papale et al [44] and references therein [45,46,47]. Cell-specific enzymatic activity was determined by normalizing the total (bulk) enzymatic activity to the prokaryotic cell abundance, taking into account the initial dilution of the brine samples.…”
Section: Methodsmentioning
confidence: 99%
“…The extracted DNAs were used to amplify the V1-V2 region of 16S rRNA gene of Bacteria (primers 27f 5′-AGAGTTTGATCCTGGCTCAG-3′ and 338 5′-GCT GCC TCC CGT AGG AGT -3′) and the most conserved V3-V4 region of Archaea (primers ARC344f 5′-ACGGGGYGCAGCAGGCGCGA-3′ and 693r 5′-GGATTACARGATTTC-3′). Two PCR amplifications (in duplicate) were performed according to Papale et al [44]. Briefly, in order to reduce biases in massive sequencing, a two-step PCR protocol was applied: the first step consisted of a conventional PCR, and then amplicons were used as templates in the second PCR with barcoded primers for Ion Torrent sequencing.…”
Section: Methodsmentioning
confidence: 99%
“…It has been suggested [ 46 ] that Burkholderiales, diazotropic Betaproteobacteria, may also play an important role in N input in newly colonized soils. Other taxa, including Actinobacteria (genus Streptomyces and family Frankeniaceae ) and Chloroflexi, are involved in nitrogen fixation in Antarctic soils [ 44 , 45 ], although their quantitative contributions are unknown.…”
Section: N-cycling Taxa In Soilsmentioning
confidence: 99%
“…Nonetheless, a recent multi -omics approach (culture-independent technique) showed the prokaryotic community occurring within the active layer at Edmonson Point, an ice-free area on the eastern slope at the foot of Mount Melbourne (Northern Victoria Land, Antarctica) [40]. The composition of this area—from more to less abundant—showed Proteobacteria, Actinobacteria, Acidobacteria, Bacteroidetes, Planctomycetes, Chloroflexi, and Verrucomicrobia [40], while Proteobacteria, Actinobacteria, Bacteroidetes, and Firmicutes have been more frequently reported through cultivation-based methods [17,34,41]. Interestingly, 16SrRNA sequencing and analysis revealed that anaerobic spore-forming Firmicutes have been shown to be the most abundant group in the Antarctic vascular plants rhizosphere [42].…”
Section: The Antarctic Environment Supports Varied Microbial Lifementioning
confidence: 99%