BCO-DMO ERDDAP
Accessing BCO-DMO data |
log in
Brought to you by BCO-DMO |
Row Type | Variable Name | Attribute Name | Data Type | Value |
---|---|---|---|---|
attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv |
attribute | NC_GLOBAL | acquisition_description | String | Seawater was collected from the San Pedro Ocean Time-series (SPOT) station off\nthe coast of Southern California near the surface (5 m), 150 and 890 m, in\nlate May 2015. Briefly, seawater was pre-filtered (80 mm) into 20 L carboys to\nminimize the presence of multicellular eukaryotes. Replicate samples (ranging\nin volume from 1.5-3.5 L) from each depth were filtered onto sterile GF/F\nfilters (nominal pore size 0.7 mm, Whatman, International Ltd. Florham Park,\nNJ). While we cannot avoid some impact that sample handling (i.e., bringing\nsamples to the surface) may have had on our results, filters were immediately\nplaced in 1.5 mL of lysis buffer and flash frozen in liquid nitrogen in < 40\nmin and away from light to minimize RNA degradation.\n \nTotal RNA was extracted from each filter using a DNA/RNA AllPrep kit (Qiagen,\nValencia, CA, #80204) with an in-line genomic DNA removal step (RNase-free\nDNase reagents, Qiagen #79254) (dx.doi.org/10.17504/protocols.io.hk3b4yn).\nExtracted RNA was quality checked and low biomass samples were pooled. Six\nreplicates were processed and sequenced from the surface, while pairs of\nfilters were pooled for either 150 or 890 m, yielding 3 and 4 replicates\nrespectively (Supporting Information Table S1). RNA concentrations were\nnormalized before library preparation (Supporting Information). ERCC spike-in\nwas added before sequence library preparation with Kapa\\u2019s Stranded mRNA\nlibrary preparation kit using poly-A tail selection beads to select for\neukaryotic mRNA (Kapa Biosystems, Inc., Wilmington, MA, #KK8420).\n \nAlso see:\n \n[https://www.protocols.io/view/sample-collection-from-the-field-for-\ndowns...](\\\\\"https://www.protocols.io/view/sample-collection-from-the-field-\nfor-downstream-mo-hisb4eehttps://www.protocols.io/view/rna-and-optional-dna-\nextraction-from-environmental-hk3b4yn\\\\\")\n \nThe associated assembly files can be found at Zenodo (see Hu, S. K. (2017),\nDOI:\\u00a010.5281/zenodo.1202041).\\u00a0 The assembly files were also\npublished in the journal publication Hu, et al. (2018).\n \nRelated code can be found in the github repository\n[https://github.com/shu251/SPOT_metatranscriptome.\\u00a0](\\\\\"https://github.com/shu251/SPOT_metatranscriptome.\\\\u00a0\\\\\")\nThe version of the code used for these publications can be found in the\nSupplemental Files section of this page. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 743048 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1737409 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1737409 |
attribute | NC_GLOBAL | awards_0_funder_name | String | NSF Division of Ocean Sciences |
attribute | NC_GLOBAL | awards_0_funding_acronym | String | NSF OCE |
attribute | NC_GLOBAL | awards_0_funding_source_nid | String | 355 |
attribute | NC_GLOBAL | awards_0_program_manager | String | David L. Garrison |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50534 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | Microbial eukaryotic focused metatranscriptome data \n PI: David Caron \n Data version 2: 2020-02-26 |
attribute | NC_GLOBAL | Conventions | String | COARDS, CF-1.6, ACDD-1.3 |
attribute | NC_GLOBAL | creator_email | String | info at bco-dmo.org |
attribute | NC_GLOBAL | creator_name | String | BCO-DMO |
attribute | NC_GLOBAL | creator_type | String | institution |
attribute | NC_GLOBAL | creator_url | String | https://www.bco-dmo.org/ |
attribute | NC_GLOBAL | data_source | String | extract_data_as_tsv version 2.3 19 Dec 2019 |
attribute | NC_GLOBAL | dataset_current_state | String | Final and no updates |
attribute | NC_GLOBAL | date_created | String | 2018-09-04T20:19:13Z |
attribute | NC_GLOBAL | date_modified | String | 2020-05-11T22:00:05Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.26008/1912/bco-dmo.745518.2 |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/745518 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | Niskin bottle |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 773599 |
attribute | NC_GLOBAL | instruments_0_description | String | A Niskin bottle (a next generation water sampler based on the Nansen bottle) is a cylindrical, non-metallic water collection device with stoppers at both ends. The bottles can be attached individually on a hydrowire or deployed in 12, 24, or 36 bottle Rosette systems mounted on a frame and combined with a CTD. Niskin bottles are used to collect discrete water samples for a range of measurements including pigments, nutrients, plankton, etc. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L22/current/TOOL0412/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | Niskin bottle |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 413 |
attribute | NC_GLOBAL | instruments_1_acronym | String | Automated Sequencer |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_description | String | HiSeq High Output 125 bp PE sequencing was performed at UPC Genome Core at University of Southern California, Los Angeles, CA (BioProject: PRJNA391503). |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_nid | String | 745534 |
attribute | NC_GLOBAL | instruments_1_description | String | 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. |
attribute | NC_GLOBAL | instruments_1_instrument_name | String | Automated DNA Sequencer |
attribute | NC_GLOBAL | instruments_1_instrument_nid | String | 649 |
attribute | NC_GLOBAL | instruments_1_supplied_name | String | HiSeq |
attribute | NC_GLOBAL | keywords | String | accession, bco, bco-dmo, biological, bioproject, bioproject_accession, biosample, biosample_accession, chemical, data, dataset, description, design, design_description, dmo, erddap, filename, filename2, filetype, instrument, instrument_model, layout, library, library_ID, library_layout, library_selection, library_source, library_strategy, link, management, model, name, oceanography, office, platform, preliminary, run, sample, sample_name, selection, source, sra, SRA_run, SRA_run_link, SRA_study, strategy, study, title |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/745518/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/745518 |
attribute | NC_GLOBAL | param_mapping | String | {'745518': {}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/745518/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of Southern California |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | USC |
attribute | NC_GLOBAL | people_0_person_name | String | David Caron |
attribute | NC_GLOBAL | people_0_person_nid | String | 50524 |
attribute | NC_GLOBAL | people_0_role | String | Principal Investigator |
attribute | NC_GLOBAL | people_0_role_type | String | originator |
attribute | NC_GLOBAL | people_1_affiliation | String | University of Southern California |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | USC |
attribute | NC_GLOBAL | people_1_person_name | String | Sarah K. Hu |
attribute | NC_GLOBAL | people_1_person_nid | String | 745520 |
attribute | NC_GLOBAL | people_1_role | String | Co-Principal Investigator |
attribute | NC_GLOBAL | people_1_role_type | String | originator |
attribute | NC_GLOBAL | people_2_affiliation | String | University of Southern California |
attribute | NC_GLOBAL | people_2_affiliation_acronym | String | USC |
attribute | NC_GLOBAL | people_2_person_name | String | Sarah K. Hu |
attribute | NC_GLOBAL | people_2_person_nid | String | 745520 |
attribute | NC_GLOBAL | people_2_role | String | Contact |
attribute | NC_GLOBAL | people_2_role_type | String | related |
attribute | NC_GLOBAL | people_3_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_3_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_3_person_name | String | Amber D. York |
attribute | NC_GLOBAL | people_3_person_nid | String | 643627 |
attribute | NC_GLOBAL | people_3_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_3_role_type | String | related |
attribute | NC_GLOBAL | project | String | SPOT |
attribute | NC_GLOBAL | projects_0_acronym | String | SPOT |
attribute | NC_GLOBAL | projects_0_description | String | Planktonic marine microbial communities consist of a diverse collection of bacteria, archaea, viruses, protists (phytoplankton and protozoa) and small animals (metazoan). Collectively, these species are responsible for virtually all marine pelagic primary production where they form the basis of food webs and carry out a large fraction of respiratory processes. Microbial interactions include the traditional role of predation, but recent research recognizes the importance of parasitism, symbiosis and viral infection. Characterizing the response of pelagic microbial communities and processes to environmental influences is fundamental to understanding and modeling carbon flow and energy utilization in the ocean, but very few studies have attempted to study all of these assemblages in the same study. This project is comprised of long-term (monthly) and short-term (daily) sampling at the San Pedro Ocean Time-series (SPOT) site. Analysis of the resulting datasets investigates co-occurrence patterns of microbial taxa (e.g. protist-virus and protist-prokaryote interactions, both positive and negative) indicating which species consistently co-occur and potentially interact, followed by examination gene expression to help define the underlying mechanisms. This study augments 20 years of baseline studies of microbial abundance, diversity, rates at the site, and will enable detection of low-frequency changes in composition and potential ecological interactions among microbes, and their responses to changing environmental forcing factors. These responses have important consequences for higher trophic levels and ocean-atmosphere feedbacks. The broader impacts of this project include training graduate and undergraduate students, providing local high school student with summer lab experiences, and PI presentations at local K-12 schools, museums, aquaria and informal learning centers in the region. Additionally, the PIs advise at the local, county and state level regarding coastal marine water quality.\nThis research project is unique in that it is a holistic study (including all microbes from viruses to small metazoa) of microbial species diversity and ecological activities, carried out at the SPOT site off the coast of southern California. In studying all microbes simultaneously, this work aims to identify important ecological interactions among microbial species, and identify the basis(es) for those interactions. This research involves (1) extensive analyses of prokaryote (archaean and bacterial) and eukaryote (protistan and micro-metazoan) diversity via the sequencing of marker genes, (2) studies of whole-community gene expression by eukaryotes and prokaryotes in order to identify key functional characteristics of microorganismal groups and the detection of active viral infections, and (3) metagenomic analysis of viruses and bacteria to aid interpretation of transcriptomic analyses using genome-encoded information. The project includes exploratory metatranscriptomic analysis of poorly-understood aphotic and hypoxic-zone protists, to examine their stratification, functions and hypothesized prokaryotic symbioses. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2021-07 |
attribute | NC_GLOBAL | projects_0_geolocation | String | San Pedro Channel off the coast of Los Angeles |
attribute | NC_GLOBAL | projects_0_name | String | Protistan, prokaryotic, and viral processes at the San Pedro Ocean Time-series |
attribute | NC_GLOBAL | projects_0_project_nid | String | 743049 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2017-08 |
attribute | NC_GLOBAL | publisher_name | String | Biological and Chemical Oceanographic Data Management Office (BCO-DMO) |
attribute | NC_GLOBAL | publisher_type | String | institution |
attribute | NC_GLOBAL | sourceUrl | String | (local files) |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | subsetVariables | String | library_strategy,library_source,library_selection,library_layout,platform,instrument_model,design_description,filetype |
attribute | NC_GLOBAL | summary | String | Seawater was collected via Niskin bottles mounted with a CTD from the San Pedro Ocean Time-series (SPOT) station off the coast of Southern California near the surface (5 m), 150 and 890 m, in late May 2015. Raw sequence data was generated as part of a metatranscriptome study targeting the protistan community. Raw sequences are available at the National Center for Biotechnology Information (NCBI) Sequence Read Archive (SRA) database (SRA Study ID: SRP110974, BioProject: PRJNA391503). Sequences for BioProject PRJNA608423 will be available at NCBI on Jan 1st, 2021.\\r\\n\\r\\nThese data were published in Hu et al. (2018). |
attribute | NC_GLOBAL | title | String | [Microbial eukaryotic focused metatranscriptome data] - Microbial eukaryotic focused metatranscriptome data from seawater collected in coastal California in May of 2015 (Protistan, prokaryotic, and viral processes at the San Pedro Ocean Time-series) |
attribute | NC_GLOBAL | version | String | 2 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.5 |
variable | SRA_run | String | ||
attribute | SRA_run | bcodmo_name | String | accession number |
attribute | SRA_run | description | String | SRA Run identifier at NCBI |
attribute | SRA_run | long_name | String | SRA Run |
attribute | SRA_run | units | String | unitless |
variable | SRA_run_link | String | ||
attribute | SRA_run_link | bcodmo_name | String | external_link |
attribute | SRA_run_link | description | String | URL for SRA Run Page at NCBI |
attribute | SRA_run_link | long_name | String | SRA Run Link |
attribute | SRA_run_link | units | String | unitless |
variable | SRA_study | String | ||
attribute | SRA_study | bcodmo_name | String | accession number |
attribute | SRA_study | description | String | SRA study identifier at NCBI |
attribute | SRA_study | long_name | String | SRA Study |
attribute | SRA_study | units | String | unitless |
variable | bioproject_accession | String | ||
attribute | bioproject_accession | bcodmo_name | String | accession number |
attribute | bioproject_accession | description | String | BioProject accesion number at NCBI |
attribute | bioproject_accession | long_name | String | Bioproject Accession |
attribute | bioproject_accession | units | String | unitless |
variable | biosample_accession | String | ||
attribute | biosample_accession | bcodmo_name | String | accession number |
attribute | biosample_accession | description | String | BioSample accession number at NCBI |
attribute | biosample_accession | long_name | String | Biosample Accession |
attribute | biosample_accession | units | String | unitless |
variable | library_ID | String | ||
attribute | library_ID | bcodmo_name | String | sample_descrip |
attribute | library_ID | description | String | SRA title |
attribute | library_ID | long_name | String | Library ID |
attribute | library_ID | units | String | unitless |
variable | title | String | ||
attribute | title | bcodmo_name | String | sample_descrip |
attribute | title | description | String | Descriptive title of SRA accession |
attribute | title | long_name | String | Title |
attribute | title | units | String | unitless |
variable | sample_name | String | ||
attribute | sample_name | bcodmo_name | String | sample_descrip |
attribute | sample_name | description | String | Sample name |
attribute | sample_name | long_name | String | Sample Name |
attribute | sample_name | units | String | unitless |
variable | library_strategy | String | ||
attribute | library_strategy | bcodmo_name | String | sample_descrip |
attribute | library_strategy | description | String | Library strategy (\"AMPLICON\") |
attribute | library_strategy | long_name | String | Library Strategy |
attribute | library_strategy | units | String | unitless |
variable | library_source | String | ||
attribute | library_source | bcodmo_name | String | sample_descrip |
attribute | library_source | description | String | Library source (\"TRANSCRIPTOMIC\" or \"GENOMIC\") |
attribute | library_source | long_name | String | Library Source |
attribute | library_source | units | String | unitless |
variable | library_selection | String | ||
attribute | library_selection | bcodmo_name | String | sample_descrip |
attribute | library_selection | description | String | Library selection (\"PCR\") |
attribute | library_selection | long_name | String | Library Selection |
attribute | library_selection | units | String | unitless |
variable | library_layout | String | ||
attribute | library_layout | bcodmo_name | String | sample_descrip |
attribute | library_layout | description | String | Library layout (\"paired\") |
attribute | library_layout | long_name | String | Library Layout |
attribute | library_layout | units | String | unitless |
variable | platform | String | ||
attribute | platform | bcodmo_name | String | sample_descrip |
attribute | platform | description | String | Sequencing platform (\"Illumina\") |
attribute | platform | long_name | String | Platform |
attribute | platform | units | String | unitless |
variable | instrument_model | String | ||
attribute | instrument_model | bcodmo_name | String | sample_descrip |
attribute | instrument_model | description | String | Sequencing instrument model (\"Illumina MiSeq\") |
attribute | instrument_model | long_name | String | Instrument Model |
attribute | instrument_model | units | String | unitless |
variable | design_description | String | ||
attribute | design_description | bcodmo_name | String | sample_descrip |
attribute | design_description | description | String | Sequencing design description |
attribute | design_description | long_name | String | Design Description |
attribute | design_description | units | String | unitless |
variable | filetype | String | ||
attribute | filetype | bcodmo_name | String | sample_descrip |
attribute | filetype | description | String | Type of files |
attribute | filetype | long_name | String | Filetype |
attribute | filetype | units | String | unitless |
variable | filename | String | ||
attribute | filename | bcodmo_name | String | file_name |
attribute | filename | description | String | Name of file 1 (see NCBI for access) |
attribute | filename | long_name | String | Filename |
attribute | filename | units | String | unitless |
variable | filename2 | String | ||
attribute | filename2 | bcodmo_name | String | file_name |
attribute | filename2 | description | String | Name of file 2 (see NCBI for access) |
attribute | filename2 | long_name | String | Filename2 |
attribute | filename2 | units | String | unitless |