2016
DOI: 10.1080/01490451.2015.1099763
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Reproducing Authigenic Carbonate Precipitation in the Hypersaline Lake Acıgöl (Turkey) with Microbial Cultures

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Cited by 19 publications
(21 citation statements)
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“…The water level and depth of the lake changes seasonally, with maxima in March and minima in August. Changes in the lake's water level create dry muds and brine pools that often contain salt precipitation with a unique microbial community [9]. Lake Acıgöl brines are predominantly Na-Cl-SO 4 type with Mg +2 /Ca +2 ratios ranging from 5 to 9 depending on the season (Table 1).…”
Section: Site Descriptionmentioning
confidence: 99%
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“…The water level and depth of the lake changes seasonally, with maxima in March and minima in August. Changes in the lake's water level create dry muds and brine pools that often contain salt precipitation with a unique microbial community [9]. Lake Acıgöl brines are predominantly Na-Cl-SO 4 type with Mg +2 /Ca +2 ratios ranging from 5 to 9 depending on the season (Table 1).…”
Section: Site Descriptionmentioning
confidence: 99%
“…A diverse microbial consortium rather than a single microorganism is commonly involved in carbonate and phosphate precipitation in natural environments [5,9,25,26]. In this respect, saline lakes and their halophilic microorganisms give an opportunity to study effect of abiotic factors on bacterial nanoglobules formation and biomineralization processes under natural conditions.…”
Section: Introductionmentioning
confidence: 99%
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“…The sediment samples were obtained by Ekman bottom grab sampler and subsequently transported into sterile single-use 50-ml centrifuge tubes using a sterile spatula and stored at -20°C until further microbiological analysis. Microbiological analysis was performed according to the methods applied by Balci et al (2015). Shortly thereafter, genomic DNA from the sediment samples was extracted by using the MoBio UltraClean Microbial DNA Isolation Kit (Catalogue No.…”
Section: Microbiological Analysismentioning
confidence: 99%
“…Microbial diversity of the sediment samples was determined by the 16S rDNA UARR polymerase chain reaction (PCR) method (Li et al 1999;Menekse 2012;Balci et al 2015). A pair of universal primers namely, pA-F (5 0 -AGA GTTTGATCCTGGCTCAG-3 0 ) and pH-R (5 0 -AAGGAGG TGATCCAGCCGCA-3 0 ) were used for amplification (Li et al 1999).…”
Section: Microbiological Analysismentioning
confidence: 99%