Evidence map›Paper›PMID 26042105›Full record

ArticleFrontiers in microbiology2015

Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre.

Kristina M Fontanez, John M Eppley, Ty J Samo, David M Karl, Edward F DeLong

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing 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

73 citing papers in PubMed.

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13 more citing papers are in PubMed but not listed here.

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

5 authors.

Kristina M FontanezDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology Cambridge, MA, USA.
John M EppleyDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology Cambridge, MA, USA ; Department of Oceanography, School of Ocean and Earth Science and Technology, University of Hawaii Honolulu, HI, USA ; Daniel K. Inouye Center for Microbial Oceanography: Research and Education, University of Hawaii Honolulu, HI, USA.
Ty J SamoDepartment of Oceanography, School of Ocean and Earth Science and Technology, University of Hawaii Honolulu, HI, USA ; Daniel K. Inouye Center for Microbial Oceanography: Research and Education, University of Hawaii Honolulu, HI, USA ; Lawrence Livermore National Laboratory, Nuclear and Chemical Sciences Division Livermore, CA, USA.
David M KarlDepartment of Oceanography, School of Ocean and Earth Science and Technology, University of Hawaii Honolulu, HI, USA ; Daniel K. Inouye Center for Microbial Oceanography: Research and Education, University of Hawaii Honolulu, HI, USA.
Edward F DeLongDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology Cambridge, MA, USA ; Department of Oceanography, School of Ocean and Earth Science and Technology, University of Hawaii Honolulu, HI, USA ; Daniel K. Inouye Center for Microbial Oceanography: Research and Education, University of Hawaii Honolulu, HI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sinking particles mediate the transport of carbon and energy to the deep-sea, yet the specific microbes associated with sedimenting particles in the ocean's interior remain largely uncharacterized. In this study, we used particle interceptor traps (PITs) to assess the nature of particle-associated microbial communities collected at a variety of depths in the North Pacific Subtropical Gyre. Comparative metagenomics was used to assess differences in microbial taxa and functional gene repertoires in PITs containing a preservative (poisoned traps) compared to preservative-free traps where growth was allowed to continue in situ (live traps). Live trap microbial communities shared taxonomic and functional similarities with bacteria previously reported to be enriched in dissolved organic matter (DOM) microcosms (e.g., Alteromonas and Methylophaga), in addition to other particle and eukaryote-associated bacteria (e.g., Flavobacteriales and Pseudoalteromonas). Poisoned trap microbial assemblages were enriched in Vibrio and Campylobacterales likely associated with eukaryotic surfaces and intestinal tracts as symbionts, pathogens, or saprophytes. The functional gene content of microbial assemblages in poisoned traps included a variety of genes involved in virulence, anaerobic metabolism, attachment to chitinaceaous surfaces, and chitin degradation. The presence of chitinaceaous surfaces was also accompanied by the co-existence of bacteria which encoded the capacity to attach to, transport and metabolize chitin and its derivatives. Distinctly different microbial assemblages predominated in live traps, which were largely represented by copiotrophs and eukaryote-associated bacterial communities. Predominant sediment trap-assocaited eukaryotic phyla included Dinoflagellata, Metazoa (mostly copepods), Protalveolata, Retaria, and Stramenopiles. These data indicate the central role of eukaryotic taxa in structuring sinking particle microbial assemblages, as well as the rapid responses of indigenous microbial species in the degradation of marine particulate organic matter (POM) in situ in the ocean's interior.

Indexed as

biological pumpmarine particlesmetagenomicsmicrobiologysediment trap

Identifiers

PMID26042105
PMCPMC4436931

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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.