Contributors | Affiliation | Role |
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Dekas, Anne E. | Stanford University | Principal Investigator |
Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
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:
Samples were demultiplexed at the UC Davis DNA Technologies Core facility.
BCO-DMO Processing:
- replaced "na" with "nd" (no data)
File |
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nifH_amplicons.csv (Comma Separated Values (.csv), 62.29 KB) MD5:bb978997ab2d8ebe08aa42663aadd333 Primary data file for dataset ID 863192 |
Parameter | Description | Units |
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 |
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. |
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 |
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.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |