Evidence map›Paper›PMID 25303712›Full record

ArticleThe ISME journal2015

Revisiting N₂ fixation in Guerrero Negro intertidal microbial mats with a functional single-cell approach.

Dagmar Woebken, Luke C Burow, Faris Behnam, Xavier Mayali, Arno Schintlmeister, Erich D Fleming, Leslie Prufert-Bebout, Steven W Singer, Alejandro López Cortés, Tori M Hoehler and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
8.7field-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

44 citing papers in PubMed, 85 citations in OpenAlex.

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  18. NanoSIP: NanoSIMS Applications for Microbial Biology.Methods in molecular biology (Clifton, N.J.) · 2022
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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

15 authors at 7 institutions in 3 countries.

Dagmar Woebken1] Departments of Chemical Engineering, and of Civil and Environmental Engineering, Stanford University, Stanford, CA, USA [2] Exobiology Branch, NASA Ames Research Center, Moffett Field, CA, USA [3] Department of Microbiology and Ecosystem Science, Division of Microbial Ecology, University of Vienna, Vienna, Austria.
Luke C Burow1] Departments of Chemical Engineering, and of Civil and Environmental Engineering, Stanford University, Stanford, CA, USA [2] Exobiology Branch, NASA Ames Research Center, Moffett Field, CA, USA.
Faris BehnamDepartment of Microbiology and Ecosystem Science, Division of Microbial Ecology, University of Vienna, Vienna, Austria.
Xavier MayaliPhysical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA, USA.
Arno SchintlmeisterLarge-Instrument Facility for Advanced Isotope Research, University of Vienna, Vienna, Austria.
Erich D FlemingExobiology Branch, NASA Ames Research Center, Moffett Field, CA, USA.
Leslie Prufert-BeboutExobiology Branch, NASA Ames Research Center, Moffett Field, CA, USA.
Steven W SingerEarth Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Alejandro López CortésLaboratory of Geomicrobiology and Biotechnology, Northwestern Center for Biological Research (CIBNOR), La Paz, Mexico.
Tori M HoehlerExobiology Branch, NASA Ames Research Center, Moffett Field, CA, USA.
Jennifer Pett-RidgePhysical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA, USA.
Alfred M SpormannDepartments of Chemical Engineering, and of Civil and Environmental Engineering, Stanford University, Stanford, CA, USA.
Michael Wagner1] Department of Microbiology and Ecosystem Science, Division of Microbial Ecology, University of Vienna, Vienna, Austria [2] Large-Instrument Facility for Advanced Isotope Research, University of Vienna, Vienna, Austria.
Peter K WeberPhysical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA, USA.
Brad M BeboutExobiology Branch, NASA Ames Research Center, Moffett Field, CA, USA.
Ames Research Center · USLawrence Livermore National Laboratory · USEcologie Microbienne Lyon · FRLawrence Berkeley National Laboratory · USNorthwestern Medicine · USStanford University · USUniversity of Vienna · AT

Funding

Austrian Science Fund FWF P 25700European Research Council 294343
6 · The paper itself

Abstract

Photosynthetic microbial mats are complex, stratified ecosystems in which high rates of primary production create a demand for nitrogen, met partially by N₂ fixation. Dinitrogenase reductase (nifH) genes and transcripts from Cyanobacteria and heterotrophic bacteria (for example, Deltaproteobacteria) were detected in these mats, yet their contribution to N2 fixation is poorly understood. We used a combined approach of manipulation experiments with inhibitors, nifH sequencing and single-cell isotope analysis to investigate the active diazotrophic community in intertidal microbial mats at Laguna Ojo de Liebre near Guerrero Negro, Mexico. Acetylene reduction assays with specific metabolic inhibitors suggested that both sulfate reducers and members of the Cyanobacteria contributed to N₂ fixation, whereas (15)N₂ tracer experiments at the bulk level only supported a contribution of Cyanobacteria. Cyanobacterial and nifH Cluster III (including deltaproteobacterial sulfate reducers) sequences dominated the nifH gene pool, whereas the nifH transcript pool was dominated by sequences related to Lyngbya spp. Single-cell isotope analysis of (15)N₂-incubated mat samples via high-resolution secondary ion mass spectrometry (NanoSIMS) revealed that Cyanobacteria were enriched in (15)N, with the highest enrichment being detected in Lyngbya spp. filaments (on average 4.4 at% (15)N), whereas the Deltaproteobacteria (identified by CARD-FISH) were not significantly enriched. We investigated the potential dilution effect from CARD-FISH on the isotopic composition and concluded that the dilution bias was not substantial enough to influence our conclusions. Our combined data provide evidence that members of the Cyanobacteria, especially Lyngbya spp., actively contributed to N₂ fixation in the intertidal mats, whereas support for significant N₂ fixation activity of the targeted deltaproteobacterial sulfate reducers could not be found.

Indexed as

Nitrogen FixationBacteriaBiodiversityCyanobacteriaDinitrogenase ReductaseEcosystemMexicoSingle-Cell AnalysisDinitrogenase Reductase

Identifiers

PMID25303712
PMCPMC4303640
OpenAlexW2044808594

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.