» Articles » PMID: 24193962

Distribution and Activity of Bacteria in Deep Granitic Groundwaters of Southeastern Sweden

Overview
Journal Microb Ecol
Date 2013 Nov 7
PMID 24193962
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

This study investigated the distribution of bacteria in groundwater from 16 different levels in five boreholes in granite bedrock down to a maximum of 860 m. Enrichment cultures were used to assay the groups of bacteria present. Autoradiographic studies with(14)C- or(3)H-labeled formate, methanol, acetate, lactate, glucose, sodium bicarbonate, leucine, glutamine, thymidine, orN-acetyl-glucosamine were used to obtain information about bacteria active in substrate uptake. The biofilm formation potential was studied in one borehole. The chemical environment in the groundwater was anaerobic with an Eh between -112 and -383 mV, a pH usually around 8, and a temperature range of 10.2 to 20.5°C, depending on the depth. The organic content ranged between <0.5 and 9.5 mg total organic carbon liter(-1). Carbon dioxide, hydrogen, hydrogen sulfide, and methane were present in the water. The nitrate, nitrite, and phosphate concentrations were close to, or below, the detection limits, while there were detectable amounts of NH4 (+) in the range of 4 to 330 μg liter(-1). The average total number of bacteria was 2.6×10(5) bacteria ml(-1), as determined with an acridine organge direct-count (AODC) technique. The average number of bacteria that grew on a medium with 1.5 g liter(-1) of organic substrate was 7.7×10(3) colony-forming units (CFU) ml(-1). The majority of these were facultatively anaerobic, gram-negative, nonfermenting heterotrophs. Enrichment cultures indicated the presence of anaerobic bacteria capable of growth on C-1 compounds and hydrogen, presumably methanogenic bacteria. Most probable number assays with sulfate and lactate revealed up to 5.6×10(4) viable sulfate-reducing bacteria per ml. A biofilm development experiment indicated an active attached microbial population. Active substrate uptake could not be registered with the bulk water populations, except for an uptake of leucine not associated with growth. The bulk water microbial cells in deep groundwater may be inactive cells detached from active biofilms on the rock surface.

Citing Articles

Deep terrestrial indigenous microbial community dominated by Frackibacter.

Ford S, Slater G, Engel K, Warr O, Lollar G, Brady A Commun Earth Environ. 2025; 5(1):795.

PMID: 39742000 PMC: 11683007. DOI: 10.1038/s43247-024-01966-8.


mSphere of Influence: Surface Sensing in Biofilm Formation.

De Leon K mSphere. 2021; 6(3).

PMID: 33980683 PMC: 8125057. DOI: 10.1128/mSphere.00369-21.


gen. nov. sp. nov., a Novel Fumarate-Fermenting Microorganism From a Deep Fractured Carbonate Aquifer of the US Great Basin.

Hamilton-Brehm S, Stewart L, Zavarin M, Caldwell M, Lawson P, Onstott T Front Microbiol. 2019; 10:2224.

PMID: 31611860 PMC: 6776889. DOI: 10.3389/fmicb.2019.02224.


Changes in bacterial and archaeal communities during the concentration of brine at the graduation towers in Ciechocinek spa (Poland).

Kalwasinska A, Deja-Sikora E, Burkowska-But A, Szabo A, Felfoldi T, Kosobucki P Extremophiles. 2017; 22(2):233-246.

PMID: 29260386 PMC: 5847177. DOI: 10.1007/s00792-017-0992-5.


The deep, hot biosphere: Twenty-five years of retrospection.

Colman D, Poudel S, Stamps B, Boyd E, Spear J Proc Natl Acad Sci U S A. 2017; 114(27):6895-6903.

PMID: 28674200 PMC: 5502609. DOI: 10.1073/pnas.1701266114.


References
1.
Beeman R, Suflita J . Microbial ecology of a shallow unconfined ground water aquifer polluted by municipal landfill leachate. Microb Ecol. 2013; 14(1):39-54. DOI: 10.1007/BF02011569. View

2.
Kirchman D, Ducklow H, Mitchell R . Estimates of bacterial growth from changes in uptake rates and biomass. Appl Environ Microbiol. 1982; 44(6):1296-307. PMC: 242188. DOI: 10.1128/aem.44.6.1296-1307.1982. View

3.
Tabor P, Neihof R . Improved microautoradiographic method to determine individual microorganisms active in substrate uptake in natural waters. Appl Environ Microbiol. 1982; 44(4):945-53. PMC: 242121. DOI: 10.1128/aem.44.4.945-953.1982. View

4.
Strandberg G, Shumate S, PARROTT J . Microbial Cells as Biosorbents for Heavy Metals: Accumulation of Uranium by Saccharomyces cerevisiae and Pseudomonas aeruginosa. Appl Environ Microbiol. 1981; 41(1):237-45. PMC: 243671. DOI: 10.1128/aem.41.1.237-245.1981. View

5.
Meyer-Reil L . Autoradiography and epifluorescence microscopy combined for the determination of number and spectrum of actively metabolizing bacteria in natural water. Appl Environ Microbiol. 1978; 36(3):506-12. PMC: 243076. DOI: 10.1128/aem.36.3.506-512.1978. View