Evidence map›Paper›PMID 42391470›Full record

ArticleThe ISME journal2026

Minimizing decompression and warming during deep seawater collection increases abundance and activity of autochthonous bacteria and archaea.

Alvaro M Plominsky, Logan M Peoples, Matthew Norenberg, Salvador Ramirez-Flandes, Sheila Podell, Kelli K Mullane, David Casagrande, Christopher Roman, Robert Pockalny, David C Smith and 8 more

Abstract read
In one paragraph

Article in The ISME journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

18 authors.

Alvaro M PlominskyMarine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92037, United States.ORCID 0000-0003-0816-8580
Logan M PeoplesMarine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92037, United States.
Matthew NorenbergInstitute of Geophysics and Planetary Physics, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92037, United States.
Salvador Ramirez-FlandesInstituto Milenio de Oceanografía, Universidad de Concepción, Casilla 1313, Concepción 4070386, Chile.
Sheila PodellCenter for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92037, United States.ORCID 0000-0001-7073-5190
Kelli K MullaneMarine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92037, United States.
David CasagrandeGraduate School of Oceanography, University of Rhode Island, Narragansett, RI 02882, United States.
Christopher RomanGraduate School of Oceanography, University of Rhode Island, Narragansett, RI 02882, United States.
Robert PockalnyGraduate School of Oceanography, University of Rhode Island, Narragansett, RI 02882, United States.
David C SmithGraduate School of Oceanography, University of Rhode Island, Narragansett, RI 02882, United States.ORCID 0000-0003-0627-5788
Caroline BelserGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ Evry, Université Paris-Saclay, 91057 Evry Cedex, Evry, France.ORCID 0000-0002-8108-9910
Julie PoulainGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ Evry, Université Paris-Saclay, 91057 Evry Cedex, Evry, France.ORCID 0000-0002-8744-3116
Eric E AllenMarine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92037, United States.
Ronnie N GludNordcee and HADAL, Department of Biology, University of Southern Denmark, Odense M, 5230 M, Denmark.
Osvaldo UlloaInstituto Milenio de Oceanografía, Universidad de Concepción, Casilla 1313, Concepción 4070386, Chile.ORCID 0000-0002-9501-5576
Nicholas BarberDepartment of Biology, San Diego State University, San Diego, CA 92182, United States.ORCID 0000-0003-1653-0009
Steven D'HondtGraduate School of Oceanography, University of Rhode Island, Narragansett, RI 02882, United States.
Douglas H BartlettMarine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA 92037, United States.ORCID 0000-0002-8385-1139

Funding

Chilean Agency for Research and Development ICN12_019N-IMODanish National Research Foundation DNRF145France GénomiqueGenoscope-CEAHADES-ERC 669947IfremerLewis and Clark Fund for Exploration and Field Research in AstrobiologyNational Oceanic and Atmospheric Administration NA17OAR0110212National Science Foundation Ocean Technology and Interdisciplinary Coordination 1635466NIH HHS 1S10OD010786-01
6 · The paper itself

Abstract

The deep ocean hosts autochthonous pressure-adapted microorganisms that are unique to this environment, as well as allochthonous pressure-sensitive members transported from shallow depths by vertical advection and particle-sinking. However, conventional sampling instruments decompress and warm deep-sea samples during retrieval, potentially altering microbial properties when studied ex situ. Here, we assess this potential sampling bias by comparing seawater microbial communities collected with or without measures aimed at minimizing pressure and temperature effects. When compared to samples collected under pressurized conditions, conventional sampling (using Niskin bottles) was found to affect prokaryotic cells retrieved by reducing their total numbers, diminishing protein synthesis activity (>10%), and also causing overall shifts in the community composition. The most significant compositional change was a >20% decrease in metagenomic archaeal representation (TACK-group/Thaumarchaeota/Nitrososphaerota). Deep-sea bacterial groups had mixed responses to preserving pressure during retrieval, with some groups exhibiting higher representation when samples were maintained pressurized (e.g. members of the family Pelagibacteraceae, unclassified Thiotricales, Thioglobaceae, and Chitinophagaceae), whereas others increased their representation when decompressed (e.g. Burkholderiaceae, Comamonadaceae, and Oxalobacteraceae). This study reveals the existence of bias introduced by the complete decompression of samples retrieved with traditional instrumentation, as well as a decrease in overall bacterial activity when samples are completely decompressed during retrieval. Additionally, incubations lasting for >24 h were shown to transform the original prokaryotic community composition. Precautions addressing these effects are necessary to enhance the reliability of ex situ measurements and improve our understanding of deep-sea microbial ecology and biogeochemistry.

Indexed as

ArchaeaBacteriaSeawaterSpecimen HandlingMetagenomicsPressureTemperaturecell lysisdeep seametagenome-assembled-genomesmetagenomicsmicrobial activitymicrobial oceanographypiezophilepiezo-sensitivepressure

Identifiers

PMID42391470
PMCPMC13332712

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Registered trials

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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.