NCBI accession numbers describing nifH amplicon sequences from sediment samples collected offshore of San Francisco, Califronia, USA in March 2017 on R/V Oceanus cruise OC1703A

Website: https://www.bco-dmo.org/dataset/863192
Data Type: Cruise Results
Version: 1
Version Date: 2021-10-13

Project
» Nitrogen Fixation in Deep-Sea Sediments (Deep Sediment N Fix)
ContributorsAffiliationRole
Dekas, Anne E.Stanford UniversityPrincipal Investigator
Rauch, ShannonWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
These data are raw, demultiplexed nifH amplicon sequences generated from Illumina MiSeq for the investigation of potential diazotroph diversity along a continental margin transect. Raw Illumina MiSeq 2×250 bp sequence data can be accessed in the NCBI SRA database under accession numbers ERP130242 and ERP120468 and BioProject accession numbers PRJEB46054 and PRJEB37167. Data under accession number ERP120468 and BioProject accession number PRJEB37167 were published in Kapili and Dekas, 2021. The generation of these data was completed on June 29, 2021.


Coverage

Spatial Extent: N:37.134378 E:-122.544233 S:35.68905 W:-124.92211

Methods & Sampling

Sediment samples were collected using a multicorer on board the R/V Oceanus (March 2017) and sample aliquots were immediately stored at -80°C until DNA extraction. DNA was extracted in the laboratory using an RNeasy PowerSoil DNA elution kit (Qiagen, catalog no. 12867-25) after RNA was extracted using an RNeasy PowerSoil Total RNA kit. (Qiagen, catalog no. 12866-25).

nifH sequences were amplified using the PCR primers described in Mehta et al., 2003 and amplicons were prepared for 2×250 bp sequencing on an Illumina MiSeq platform following the protocol described in Kapili et al., 2020.


Data Processing Description

Data Processing:
Samples were demultiplexed at the UC Davis DNA Technologies Core facility.

BCO-DMO Processing:
- replaced "na" with "nd" (no data)


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Data Files

File
nifH_amplicons.csv
(Comma Separated Values (.csv), 62.29 KB)
MD5:bb978997ab2d8ebe08aa42663aadd333
Primary data file for dataset ID 863192

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Related Publications

Kapili, B. J., & Dekas, A. E. (2021). PPIT: an R package for inferring microbial taxonomy from nifH sequences. Bioinformatics, 37(16), 2289–2298. doi:10.1093/bioinformatics/btab100
Results
Kapili, B. J., Barnett, S. E., Buckley, D. H., & Dekas, A. E. (2020). Evidence for phylogenetically and catabolically diverse active diazotrophs in deep-sea sediment. The ISME Journal, 14(4), 971–983. doi:10.1038/s41396-019-0584-8
Methods
Mehta, M. P., Butterfield, D. A., & Baross, J. A. (2003). Phylogenetic Diversity of Nitrogenase (nifH) Genes in Deep-Sea and Hydrothermal Vent Environments of the Juan de Fuca Ridge. Applied and Environmental Microbiology, 69(2), 960–970. doi:10.1128/aem.69.2.960-970.2003
Methods

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Related Datasets

IsRelatedTo
STANFORD UNIVERSITY. PPIT: an R package for inferring microbial taxonomy from nifH sequences. 2020/09. In: BioProject [Internet]. Bethesda, MD: National Library of Medicine (US), National Center for Biotechnology Information; 2011-. Available from: http://www.ncbi.nlm.nih.gov/bioproject/PRJEB37167. NCBI:BioProject: PRJEB37167

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Parameters

ParameterDescriptionUnits
BioProject

BioProject accession

unitless
BioSample

BioSample accession

unitless
SRA_study

SRA study accession

unitless
Assay_Type

Assay type

unitless
Sequencing_platform

Squencing platform

unitless
Instrument_model

Illumina model

unitless
Library_layout

Library layout

unitless
File_name_1

File name of forward reads

unitless
File_name_2

File name of reverse reads

unitless
File_type

File type

unitless
Sequencing_method

Sequencing method

unitless
Library_selection

Library selection

unitless
PCR_primers

PCR primer sequences

unitless
Sequencing_adapters

Illumina adapter sequences

unitless
Geographic_location

Sampling location

unitless
Sample_type

Environmental sample type

unitless
Sample_name

Sample name

unitless
Sample_latitude

Sampling latitude

decimal degrees North
Sample_longitude

Sampling longitude

decimal degrees East
Deployment_number

Deployment number

unitless
Multicore_number

Mulitcore number

unitless
Seawater_depth

Seawater depth

meters below sea surface
Sediment_depth

Sediment depth

centimeters below sediment surface


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Instruments

Dataset-specific Instrument Name
Illumina MiSeq platform
Generic Instrument Name
Automated DNA Sequencer
Generic Instrument Description
General term for a laboratory instrument used for deciphering the order of bases in a strand of DNA. Sanger sequencers detect fluorescence from different dyes that are used to identify the A, C, G, and T extension reactions. Contemporary or Pyrosequencer methods are based on detecting the activity of DNA polymerase (a DNA synthesizing enzyme) with another chemoluminescent enzyme. Essentially, the method allows sequencing of a single strand of DNA by synthesizing the complementary strand along it, one base pair at a time, and detecting which base was actually added at each step.

Dataset-specific Instrument Name
MC-800
Generic Instrument Name
Multi Corer
Generic Instrument Description
The Multi Corer is a benthic coring device used to collect multiple, simultaneous, undisturbed sediment/water samples from the seafloor. Multiple coring tubes with varying sampling capacity depending on tube dimensions are mounted in a frame designed to sample the deep ocean seafloor. For more information, see Barnett et al. (1984) in Oceanologica Acta, 7, pp. 399-408.


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Deployments

OC1703A

Website
Platform
R/V Oceanus
Start Date
2017-03-14
End Date
2017-03-23
Description
See additional cruise information from the Rolling Deck to Repository (R2R): https://www.rvdata.us/search/cruise/OC1703A


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Project Information

Nitrogen Fixation in Deep-Sea Sediments (Deep Sediment N Fix)

Coverage: California Shelf (36,-123)


NSF Award Abstract:
Life requires nitrogen for growth. Atmospheric nitrogen (N2) is the most abundant form of nitrogen on the surface of the planet, but most organisms cannot assimilate N2 directly. Habitats can therefore be nitrogen limited, meaning the demand for "bioavailable" nitrogen exceeds the supply, and its availability controls the overall growth and productivity of the community. A small subset of microorganisms, termed diazotrophs, convert N2 to bioavailable forms of nitrogen, including ammonium and nitrogenous organic matter, in a process known as N2 fixation. Diazotrophs are the largest natural source of bioavailable nitrogen on the planet, and the rate at which they fix N2 can control the rates at which other important microbial processes occur, such as the production and consumption of greenhouse gases. Understanding diazotrophs in the environment - their identity, distribution, activity levels, and biogeochemical controls - is therefore essential to understanding overall microbial community activity and biogeochemical cycling. The goal of this project is to characterize N2 fixation in deep-sea sediments, a generally understudied but expansive habitat, covering nearly two thirds of our planet. The project will have broader impacts via educational outreach, support and training of early career scientists, and scientific impact: since rates of marine methane, carbon dioxide, and nitrous oxide cycling are affected by nitrogen availability, the results will inform our understanding of greenhouse gas cycling in the marine environment, and therefore climate stability, a topic central to global security.

N2 fixation is a critical and intensely studied metabolism in the marine photic zone. Much less is known about N2 fixation in deep-sea sediments, but it could be an important factor in both benthic productivity and ocean-scale elemental cycling. Several observations have suggested or directly detected N2 fixation at localized areas of enhanced productivity on the seafloor (e.g., methane seeps and hydrothermal vents), raising the possibility that deep-sea N2 fixation is widespread. However, few measurements of N2 fixation have been made outside of these anomalous areas, and thus little is known about N2 fixation in the vast majority of the deep ocean floor. Preliminary data suggest N2 fixation does occur in typical deep marine sediment, and is mediated by a diverse set of yet unidentified microorganisms. This project will combine techniques from molecular biology and geochemistry to systematically investigate N2 fixation in representative deep-sea sediments collected along a depth profile (500 to 4500 m water depth) offshore California. The project will determine the (1) rates and distribution of N2 fixation (2) abundance, diversity, and distribution of genes and transcripts associated with N2 fixation (nif) (3) phylogenetic identity of the biological mediators (diazotrophs) and (4) physiochemical controls on diazotrophic community structure and activity. For context, the activity of the non-diazotrophic bacterial community will also be characterized. The results may lead to upward revisions of the estimates of new nitrogen production in the seafloor, and therefore change our understanding of the current balance of the marine nitrogen cycle. Together, this hypothesis-driven characterization of N2 fixation in deep-sea sediments will shed light on an expansive, climatically important, and traditionally understudied habitat, and facilitate more accurate extrapolation of the rates and distribution of N2 fixation on the whole seafloor as well as the metabolic response of the seafloor community to environmental change.



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Funding

Funding SourceAward
NSF Division of Ocean Sciences (NSF OCE)

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