Evidence map›Paper›PMID 25616797›Full record

ArticleApplied and environmental microbiology2015

Large fractions of CO2-fixing microorganisms in pristine limestone aquifers appear to be involved in the oxidation of reduced sulfur and nitrogen compounds.

Martina Herrmann, Anna Rusznyák, Denise M Akob, Isabel Schulze, Sebastian Opitz, Kai Uwe Totsche, Kirsten Küsel

Open access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
9.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 114 citations in OpenAlex.

  1. Microbial ecology of shallow groundwater ecosystems.Nature reviews. Microbiology · 2026
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  14. Bolstering fitness via COThe ISME journal · 2022
    Article
  15. Microbial diversity in extreme environments.Nature reviews. Microbiology · 2022
    Review
  16. Community characteristics of autotrophic COFrontiers in microbiology · 2022
    Article
  17. Article
  18. Article
  19. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 2 countries.

Martina HerrmannAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Jena, Germany German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Leipzig, Germany.
Anna RusznyákAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Jena, Germany.
Denise M AkobAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Jena, Germany U.S. Geological Survey, Reston, Virginia, USA.
Isabel SchulzeAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Jena, Germany.
Sebastian OpitzAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Jena, Germany.
Kai Uwe TotscheDepartment of Hydrogeology, Institute of Geosciences, Friedrich Schiller University Jena, Jena, Germany.
Kirsten KüselAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Jena, Germany German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Leipzig, Germany kirsten.kuesel@uni-jena.de.
Friedrich Schiller University Jena · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The traditional view of the dependency of subsurface environments on surface-derived allochthonous carbon inputs is challenged by increasing evidence for the role of lithoautotrophy in aquifer carbon flow. We linked information on autotrophy (Calvin-Benson-Bassham cycle) with that from total microbial community analysis in groundwater at two superimposed-upper and lower-limestone groundwater reservoirs (aquifers). Quantitative PCR revealed that up to 17% of the microbial population had the genetic potential to fix CO2 via the Calvin cycle, with abundances of cbbM and cbbL genes, encoding RubisCO (ribulose-1,5-bisphosphate carboxylase/oxygenase) forms I and II, ranging from 1.14 × 10(3) to 6 × 10(6) genes liter(-1) over a 2-year period. The structure of the active microbial communities based on 16S rRNA transcripts differed between the two aquifers, with a larger fraction of heterotrophic, facultative anaerobic, soil-related groups in the oxygen-deficient upper aquifer. Most identified CO2-assimilating phylogenetic groups appeared to be involved in the oxidation of sulfur or nitrogen compounds and harbored both RubisCO forms I and II, allowing efficient CO2 fixation in environments with strong oxygen and CO2 fluctuations. The genera Sulfuricella and Nitrosomonas were represented by read fractions of up to 78 and 33%, respectively, within the cbbM and cbbL transcript pool and accounted for 5.6 and 3.8% of 16S rRNA sequence reads, respectively, in the lower aquifer. Our results indicate that a large fraction of bacteria in pristine limestone aquifers has the genetic potential for autotrophic CO2 fixation, with energy most likely provided by the oxidation of reduced sulfur and nitrogen compounds.

Indexed as

BiotaCalcium CarbonateAutotrophic ProcessesBacteriaCarbon DioxideCluster AnalysisDNA, BacterialDNA, RibosomalGroundwaterMolecular Sequence DataNitrogen CompoundsOxidation-ReductionPhylogenyRNA, Ribosomal, 16SSequence Analysis, DNASulfur CompoundsCalcium CarbonateCarbon DioxideDNA, BacterialDNA, RibosomalNitrogen CompoundsRNA, Ribosomal, 16SSulfur Compounds

Identifiers

PMID25616797
PMCPMC4357952
OpenAlexW2034215661

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.