Evidence map›Paper›PMID 27598790›Full record

ArticlePloS one2016

Patterns of Transcript Abundance of Eukaryotic Biogeochemically-Relevant Genes in the Amazon River Plume.

Brian L Zielinski, Andrew E Allen, Edward J Carpenter, Victoria J Coles, Byron C Crump, Mary Doherty, Rachel A Foster, Joaquim I Goes, Helga R Gomes, Raleigh R Hood and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
7.7field-weighted citation impact, top 3% 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

7 citing papers in PubMed, 53 citations in OpenAlex.

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  3. The rate and fate of NThe ISME journal · 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

18 authors at 12 institutions in 3 countries.

Brian L ZielinskiUniversity of South Florida College of Marine Science, St. Petersburg, FL, United States of America.ORCID http://orcid.org/0000-0001-9432-0109
Andrew E AllenDepartment of Microbial and Environmental Genomics, J. Craig Venter Institute, San Diego, CA, United States of America.
Edward J CarpenterRomberg Tiburon Center, San Francisco State University, Tiburon, California, United States of America.
Victoria J ColesHorn Point Laboratory, University of Maryland Center for Environmental Science, Cambridge, MD, United States of America.
Byron C CrumpCollege of Earth, Ocean, and Atmospheric Sciences, Oregon State University, Corvallis, Oregon, United States of America.
Mary DohertyRhodes College, Memphis, TN, United States of America.
Rachel A FosterOcean Sciences, University of California, Santa Cruz, CA, United States of America.
Joaquim I GoesLamont Doherty Earth Observatory, Columbia University, Palisades, NY, United States of America.
Helga R GomesLamont Doherty Earth Observatory, Columbia University, Palisades, NY, United States of America.
Raleigh R HoodHorn Point Laboratory, University of Maryland Center for Environmental Science, Cambridge, MD, United States of America.
John P McCrowDepartment of Microbial and Environmental Genomics, J. Craig Venter Institute, San Diego, CA, United States of America.
Joseph P MontoyaSchool of Biology, Georgia Institute of Technology, Atlanta, GA, United States of America.
Ahmed MoustafaDepartment of Biology and Biotechnology Graduate Program, American University in Cairo, New Cairo, Egypt.
Brandon M SatinskyDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA, United States of America.
Shalabh SharmaDepartment of Marine Sciences, University of Georgia, Athens, GA, United States of America.
Christa B SmithDepartment of Marine Sciences, University of Georgia, Athens, GA, United States of America.
Patricia L YagerDepartment of Marine Sciences, University of Georgia, Athens, GA, United States of America.
John H PaulUniversity of South Florida College of Marine Science, St. Petersburg, FL, United States of America.
University of Georgia · USJ. Craig Venter Institute · USLamont-Doherty Earth Observatory · USUniversity of Maryland Center for Environmental Science · USUniversity of South Florida St. Petersburg · USAmerican University in Cairo · EGGeorgia Institute of Technology · USMassachusetts Institute of Technology · USOregon State University · USRhodes College · USSan Francisco State University · USStockholm University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Amazon River has the largest discharge of all rivers on Earth, and its complex plume system fuels a wide array of biogeochemical processes, across a large area of the western tropical North Atlantic. The plume thus stimulates microbial processes affecting carbon sequestration and nutrient cycles at a global scale. Chromosomal gene expression patterns of the 2.0 to 156 μm size-fraction eukaryotic microbial community were investigated in the Amazon River Plume, generating a robust dataset (more than 100 million mRNA sequences) that depicts the metabolic capabilities and interactions among the eukaryotic microbes. Combining classical oceanographic field measurements with metatranscriptomics yielded characterization of the hydrographic conditions simultaneous with a quantification of transcriptional activity and identity of the community. We highlight the patterns of eukaryotic gene expression for 31 biogeochemically significant gene targets hypothesized to be valuable within forecasting models. An advantage to this targeted approach is that the database of reference sequences used to identify the target genes was selectively constructed and highly curated optimizing taxonomic coverage, throughput, and the accuracy of annotations. A coastal diatom bloom highly expressed nitrate transporters and carbonic anhydrase presumably to support high growth rates and enhance uptake of low levels of dissolved nitrate and CO2. Diatom-diazotroph association (DDA: diatoms with nitrogen fixing symbionts) blooms were common when surface salinity was mesohaline and dissolved nitrate concentrations were below detection, and hence did not show evidence of nitrate utilization, suggesting they relied on ammonium transporters to aquire recently fixed nitrogen. These DDA blooms in the outer plume had rapid turnover of the photosystem D1 protein presumably caused by photodegradation under increased light penetration in clearer waters, and increased expression of silicon transporters as silicon became limiting. Expression of these genes, including carbonic anhydrase and transporters for nitrate and phosphate, were found to reflect the physiological status and biogeochemistry of river plume environments. These relatively stable patterns of eukaryotic transcript abundance occurred over modest spatiotemporal scales, with similarity observed in sample duplicates collected up to 2.45 km in space and 120 minutes in time. These results confirm the use of metatranscriptomics as a valuable tool to understand and predict microbial community function.

Indexed as

MetagenomeWater MicrobiologyDiatomsEukaryotaGene Expression RegulationHigh-Throughput Nucleotide SequencingNitrogenNitrogen FixationRiversTranscriptomeNitrogen

Identifiers

PMID27598790
PMCPMC5012681
OpenAlexW2515945356

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.