2020
DOI: 10.1038/s41598-020-68661-4
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Geobiochemistry characteristics of rare earth elements in soil and ground water: a case study in Baotou, China

Abstract: the distribution of rare earth elements and the microbial community in nearby ground water and soil were influenced by tailings ponds. Accordingly, the behaviors of rare earth elements in ground water and soil around the tailings pond, and the changes of microbial communities were both investigated in this study. The results showed that rare earth elements accumulated in ground water and soil around the tailings pond appeared as light rare earth elements enrichment. Through the normalization of rare earth elem… Show more

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Cited by 26 publications
(11 citation statements)
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“…The DNA extract was checked on a 1% agarose gel, and the DNA concentration and purity were determined with a NanoDrop 2000 UV-Vis spectrophotometer (Thermo Fisher Scientific, Wilmington, United States). The V3-V4 hypervariable region of the bacterial 16S rRNA gene was amplified with the primer pair 338F (5 -ACTCCTACGGGAGGCAGCAG-3 ) and 806R (5 -GGACTACHVGGGTWTCTAAT-3 ) by an ABI GeneAmp R 9700 PCR thermocycler (ABI, CA, United States), with an eight-base sequence barcode unique to each sample at the 5' end of 338F and 806R (Tang et al, 2020). PCR amplification of the 16S rRNA gene was performed as follows: initial denaturation at 95 • C. The PCR mixtures contained 5 × TransStart FastPfu buffer (4 µL), 2.5 mM dNTPs (2 µL), 5 µM forward primer (0.8 µL), 5 µM reverse primer (0.8 µL), TransStart FastPfu DNA Polymerase (0.4 µL), template DNA (10 ng), and ddH2O (up to 20 µL).…”
Section: Dna Extraction and Pcr Amplificationmentioning
confidence: 99%
“…The DNA extract was checked on a 1% agarose gel, and the DNA concentration and purity were determined with a NanoDrop 2000 UV-Vis spectrophotometer (Thermo Fisher Scientific, Wilmington, United States). The V3-V4 hypervariable region of the bacterial 16S rRNA gene was amplified with the primer pair 338F (5 -ACTCCTACGGGAGGCAGCAG-3 ) and 806R (5 -GGACTACHVGGGTWTCTAAT-3 ) by an ABI GeneAmp R 9700 PCR thermocycler (ABI, CA, United States), with an eight-base sequence barcode unique to each sample at the 5' end of 338F and 806R (Tang et al, 2020). PCR amplification of the 16S rRNA gene was performed as follows: initial denaturation at 95 • C. The PCR mixtures contained 5 × TransStart FastPfu buffer (4 µL), 2.5 mM dNTPs (2 µL), 5 µM forward primer (0.8 µL), 5 µM reverse primer (0.8 µL), TransStart FastPfu DNA Polymerase (0.4 µL), template DNA (10 ng), and ddH2O (up to 20 µL).…”
Section: Dna Extraction and Pcr Amplificationmentioning
confidence: 99%
“…In addition, the aluminosilicates in Al-rich CFAs may also host REYs. Another possibility is that, to some extent, Mn­(II) can also form hydroxides or oxides of ferromanganese with the EPR spectral feature of type (c) to adsorb or complex REYs. …”
Section: Resultsmentioning
confidence: 99%
“…8 The genetic types and chemical nature of REEs cause the fractionation of REEs in the coal seam. 9,10 The heavy REEs (HREEs) including Eu, Tb, Gd, Y, Lu, Dy, Tm, Ho, and Er are reported to be present at high concentration in the coals with low ash content, whereas their concentrations are low in the coals with high ash content. 11 Desorption and leaching of HREEs from tonsteins, clays, and other rocks are higher than light REEs (LREEs).…”
Section: Introductionmentioning
confidence: 99%