Literature DB >> 24190396

Density, activity, and diversity of bacteria indigenous to a karstic aquifer.

K J Rusterholtz1, L M Mallory.   

Abstract

The microbial ecology of karstic ground water is largely unknown. The density, activity, and diversity of bacteria indigenous to subsurface karstic material in Mammoth Cave National Park, Mammoth Cave, Kentucky were studied using minimally disruptive, on-site procedures. Two sites, located 100 m below the surface and consisting of saturated fine to coarse sand in pooled water, were examined. Samples were taken aseptically using modified, sterile 60-cc syringes. Total cell and total respiring cell densities were determined using an acridine orange/p-iodonitrotetrazolium violet (AO/INT) staining procedure. Cells in selected cores were stained with INT and incubated in the cave for 4 h prior to fixing with glutaraldehyde and subsequent transport to the laboratory. Cells were stained with AO in the laboratory. Low- and high-nutrient media were used to determine viable cell counts. Plates were incubated in the cave for 1 day at ambient temperature prior to transportation to the laboratory in an insulated cooler. Viable cell counts ranged from 1.0 × 106 to 8.1 × 106 cells wet g(-1) of sediment. Total direct counts were 3.9 × 106 and 1.4 × 107 cells wet g(-1) for the Olivia's Dome and the Catherine's Dome sites, respectively. Viable cell counts were highly similar to respiring cell counts at both sites. At the Olivia's Dome site, viable cell counts represented 26-31% of the direct cell counts, while 58% of the total cell count were actively respiring. At the Catherine's Dome site, viable cell counts represented 11-58% of the direct counts, while 53% of the cells were actively respiring. A total of 237 strains recovered from low- and high-nutrient media at both Olivia's and Catherine's Domes, and 10 reference strains were examined for 117 morphological, biochemical, and physiological characteristics. Results were coded in a binary fashion and analyzed using numerical taxonomic techniques. Similarity values were calculated using a simple matching coefficient. Fifty-two clusters, ranging in size from 2 to 13 members, were defined at the 80-85% similarity level with the weighted pair-group mathematical average algorithm (WPGMA). The matrix was examined using the Jaccard coefficient and WPGMA clustering to control for distortion due to negative matches and varying group size. Presumptively identified genera include, Arthrobacter, Brevibacterium, Bacillus, Cornyebacterium, Actinomyces, Aureobacterium, Chromobacterium, and Mycobacterium. Pseudomonas spp. were not recovered. Fifty percent of the clustered operational taxonomic units (OTUs) were not identified. Thirty percent of the clustered OTUs were irregular, asporogenous, Gram-positive rods. The bacterial communities varied between sites, and isolation medium had a strong influence on the strains recovered. The bacterial community in the karstic sediments sampled exhibits a high degree of diversity having no dominant strain or strains.

Entities:  

Year:  1994        PMID: 24190396     DOI: 10.1007/BF00170249

Source DB:  PubMed          Journal:  Microb Ecol        ISSN: 0095-3628            Impact factor:   4.552


  16 in total

1.  Simplified tests for some amino acid decarboxylases and for the arginine dihydrolase system.

Authors:  V MØLLER
Journal:  Acta Pathol Microbiol Scand       Date:  1955

2.  The taxonomic significance of fermentative versus oxidative metabolism of carbohydrates by various gram negative bacteria.

Authors:  R HUGH; E LEIFSON
Journal:  J Bacteriol       Date:  1953-07       Impact factor: 3.490

3.  Physiological diversity and distributions of heterotrophic bacteria in deep cretaceous sediments of the atlantic coastal plain.

Authors:  J K Fredrickson; D L Balkwill; J M Zachara; S M Li; F J Brockman; M A Simmons
Journal:  Appl Environ Microbiol       Date:  1991-02       Impact factor: 4.792

4.  Heterotrophic bacterial guild structure: Relationship to biodegradative populations.

Authors:  L M Mallory; G S Sayler
Journal:  Microb Ecol       Date:  1983-04       Impact factor: 4.552

5.  Microbial communities in the saturated groundwater environment I: Methods of isolation and characterization of heterotrophic bacteria.

Authors:  J Kölbel-Boelke; B Tienken; A Nehrkorn
Journal:  Microb Ecol       Date:  1988-07       Impact factor: 4.552

6.  Distribution and activity of microorganisms in subsurface sediments of a pristine study site in Oklahoma.

Authors:  R M Beloin; J L Sinclair; W C Ghiorse
Journal:  Microb Ecol       Date:  1988-07       Impact factor: 4.552

7.  Morphological and cultural comparison of microorganisms in surface soil and subsurface sediments at a pristine study site in Oklahoma.

Authors:  T L Bone; D L Balkwill
Journal:  Microb Ecol       Date:  1988-07       Impact factor: 4.552

8.  Microbial communities in the saturated groundwater environment II: Diversity of bacterial communities in a Pleistocene sand aquifer and their in vitro activities.

Authors:  J Kölbel-Boelke; E M Anders; A Nehrkorn
Journal:  Microb Ecol       Date:  1988-07       Impact factor: 4.552

9.  A multipoint inoculator for petri dishes.

Authors:  T E Lovelace; R R Colwell
Journal:  Appl Microbiol       Date:  1968-06

10.  Utilization of aromatic hydrocarbons by Arthrobacter spp.

Authors:  I L Stevenson
Journal:  Can J Microbiol       Date:  1967-02       Impact factor: 2.419

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  1 in total

1.  Heterotrophic prokaryotic production in ultraoligotrophic alpine karst aquifers and ecological implications.

Authors:  Inés C Wilhartitz; Alexander K T Kirschner; Hermann Stadler; Gerhard J Herndl; Martin Dietzel; Christine Latal; Robert L Mach; Andreas H Farnleitner
Journal:  FEMS Microbiol Ecol       Date:  2009-06       Impact factor: 4.194

  1 in total

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