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,.esriCsv,.geoJson |
attribute | NC_GLOBAL | acquisition_description | String | Nine species of diatoms were isolated from the Western Antarctic Peninsula\nalong the PalmerLTER sampling grid in 2013 and 2014. Isolations were performed\nusing an Olympus CKX41 inverted microscope by single cell isolation with a\nmicropipette (Anderson 2005). Diatom species were identified by morphological\ncharacterization and 18S rRNA gene (rDNA) sequencing. DNA was extracted with\nthe DNeasy Plant Mini Kit according to the manufacturer\\u2019s protocols\n(Qiagen). Amplification of the nuclear 18S rDNA region was achieved with\nstandard PCR protocols using eukaryotic-specific, universal 18S forward and\nreverse primers. Primer sequences were obtained from Medlin et al. (1982). The\nlength of the region amplified is approximately 1800 base pairs (bp\n).\\u00a0Pseudo-nitzschia\\u00a0species are often difficult to identify by their\n18S rDNA sequence, therefore, additional support of the taxonomic\nidentification of\\u00a0P.\\u00a0subcurvata\\u00a0was provided through sequencing\nof the 18S-ITS1-5.8S regions. Amplification of this region was performed with\nthe 18SF-euk and 5.8SR_euk primers of Hubbard et al. (2008). PCR products were\npurified using either QIAquick PCR Purification Kit (Qiagen) or ExoSAP-IT\n(Affymetrix) and sequenced by Sanger DNA sequencing (Genewiz). Sequences were\nedited using Geneious Pro software\n([http://www.geneious.com](\\\\\"http://www.geneious.com\\\\\"), Kearse et al.,\n2012) and BLASTn sequence homology searches were performed against the NCBI\nnucleotide non-redundant (nr) database to determine species with a cutoff\nidentity of 98%.\n \nIllumina TruSeq adapters and poly-A tails were trimmed from raw reads using\nthe Fastx_toolkit clipper function. Fastq_quality_filter was used to remove\npoor quality sequences, such that remaining sequences had a minimum quality\nscore of 20 with a minimum of 80% of bases within a\\u00a0read\\u00a0meeting\nthis quality score requirement. Any remaining raw sequences less than 50 base\npairs in length were also removed. Merged files were assembled\\u00a0de\nnovo\\u00a0using Trinity (Grabherr et al. 2011). The resulting assembly was\nfiltered to remove contigs less than 200 bp in length. Trinity-assembled\ncontigs which exhibited sequence overlap were grouped into isogroups which\nwere then used for sequence homology searches (BLASTx E-value \\u2264 10-4)\nagainst the Kyoto Encyclopedia of Genes and Genomes (KEGG) databases (Kanehisa\n2006).\n \nGene biogeographical distributions -\\u00a020 genes of interest were selected\nin the study to investigate the molecular basis of iron and light limitation\nin polar diatoms. Reference sequences for each of these genes were obtained\nfrom the\\u00a0F.\\u00a0cylindrus\\u00a0and\\u00a0P.\\u00a0tricornutum\\u00a0JGI\ngenome portals\nand\\u00a0T.\\u00a0pseudonana\\u00a0and\\u00a0T.\\u00a0oceanica\\u00a0NCBI and\nGenBank repositories. Reference sequences were identified in the\ntranscriptomes by translated nucleotide homology searches (tBLASTn) with an\ne-value cutoff of <10-5. A reciprocal tBLASTn homology search was performed\nfor each transcriptome against the KEGG GENES database, using the single-\ndirectional\\u00a0best-hit\\u00a0method in the KAAS online tool to ensure\nconsistent gene annotations (Moriya et al. 2007).\n \nSubsequently, reference sequences were identified in the MMETSP protein\ndatabase by BLASTp (e-value <10-5) homology searches among the diatom\ntranscriptomes. The transcriptomes and their associated latitude and longitude\nwere obtained from iMicrobe Data Commons (Project Code CAM_P_0001000) and the\nNational Center for Marine Algae and Microbiota (NCMA). Custom Matlab scripts\nallowed global biogeographical distribution of key genes of interest to be\nmapped. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 653228 |
attribute | NC_GLOBAL | awards_0_award_number | String | PLR-1341479 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1341479 |
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 | Dr Chris H. Fritsen |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50502 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | BLASTp Homology Data \n Adrian Marchetti, PI \n Version 11 October 2016 |
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 | date_created | String | 2016-11-21T21:11:01Z |
attribute | NC_GLOBAL | date_modified | String | 2019-06-11T16:47:19Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.665454.1 |
attribute | NC_GLOBAL | Easternmost_Easting | double | 163.0 |
attribute | NC_GLOBAL | geospatial_lat_max | double | 77.8333 |
attribute | NC_GLOBAL | geospatial_lat_min | double | -77.8333 |
attribute | NC_GLOBAL | geospatial_lat_units | String | degrees_north |
attribute | NC_GLOBAL | geospatial_lon_max | double | 163.0 |
attribute | NC_GLOBAL | geospatial_lon_min | double | -159.4166667 |
attribute | NC_GLOBAL | geospatial_lon_units | String | degrees_east |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/665454 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | Inverted Microscope |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | Used to perform isolations |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 665461 |
attribute | NC_GLOBAL | instruments_0_description | String | An inverted microscope is a microscope with its light source and condenser on the top, above the stage pointing down, while the objectives and turret are below the stage pointing up. It was invented in 1850 by J. Lawrence Smith, a faculty member of Tulane University (then named the Medical College of Louisiana).\n\nInverted microscopes are useful for observing living cells or organisms at the bottom of a large container (e.g. a tissue culture flask) under more natural conditions than on a glass slide, as is the case with a conventional microscope. Inverted microscopes are also used in micromanipulation applications where space above the specimen is required for manipulator mechanisms and the microtools they hold, and in metallurgical applications where polished samples can be placed on top of the stage and viewed from underneath using reflecting objectives.\n\nThe stage on an inverted microscope is usually fixed, and focus is adjusted by moving the objective lens along a vertical axis to bring it closer to or further from the specimen. The focus mechanism typically has a dual concentric knob for coarse and fine adjustment. Depending on the size of the microscope, four to six objective lenses of different magnifications may be fitted to a rotating turret known as a nosepiece. These microscopes may also be fitted with accessories for fitting still and video cameras, fluorescence illumination, confocal scanning and many other applications. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB05/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | Inverted Microscope |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 675 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | Olympus CKX41 |
attribute | NC_GLOBAL | instruments_1_acronym | String | Bioanalyzer |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_description | String | Used to determine RNA integrity |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_nid | String | 665464 |
attribute | NC_GLOBAL | instruments_1_description | String | A Bioanalyzer is a laboratory instrument that provides the sizing and quantification of DNA, RNA, and proteins. One example is the Agilent Bioanalyzer 2100. |
attribute | NC_GLOBAL | instruments_1_instrument_name | String | Bioanalyzer |
attribute | NC_GLOBAL | instruments_1_instrument_nid | String | 626182 |
attribute | NC_GLOBAL | instruments_1_supplied_name | String | Agilent Bioanalyzer 2100 |
attribute | NC_GLOBAL | keywords | String | bco, bco-dmo, biological, chemical, clade, data, dataset, dmo, e_value, erddap, gene, genus, latitude, longitude, management, mmetsp, MMETSP_ID, oceanography, office, preliminary, species, strain, subject, subject_ID, value |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/665454/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/665454 |
attribute | NC_GLOBAL | Northernmost_Northing | double | 77.8333 |
attribute | NC_GLOBAL | param_mapping | String | {'665454': {'lat': 'master - latitude', 'lon': 'master - longitude'}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/665454/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of North Carolina at Chapel Hill |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | UNC-Chapel Hill |
attribute | NC_GLOBAL | people_0_person_name | String | Adrian Marchetti |
attribute | NC_GLOBAL | people_0_person_nid | String | 527120 |
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 North Carolina at Chapel Hill |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | UNC-Chapel Hill |
attribute | NC_GLOBAL | people_1_person_name | String | Adrian Marchetti |
attribute | NC_GLOBAL | people_1_person_nid | String | 527120 |
attribute | NC_GLOBAL | people_1_role | String | Contact |
attribute | NC_GLOBAL | people_1_role_type | String | related |
attribute | NC_GLOBAL | people_2_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_2_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_2_person_name | String | Hannah Ake |
attribute | NC_GLOBAL | people_2_person_nid | String | 650173 |
attribute | NC_GLOBAL | people_2_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_2_role_type | String | related |
attribute | NC_GLOBAL | project | String | Polar_Transcriptomes |
attribute | NC_GLOBAL | projects_0_acronym | String | Polar_Transcriptomes |
attribute | NC_GLOBAL | projects_0_description | String | The Southern Ocean surrounding Antarctica is changing rapidly in response to Earth's warming climate. These changes will undoubtedly influence communities of primary producers (the organisms at the base of the food chain, particularly plant-like organisms using sunlight for energy) by altering conditions that influence their growth and composition. Because primary producers such as phytoplankton play an important role in global biogeochemical cycling, it is essential to understand how they will respond to changes in their environment. The growth of phytoplankton in certain regions of the Southern Ocean is constrained by steep gradients in chemical and physical properties that vary in both space and time. Light and iron have been identified as key variables influencing phytoplankton abundance and distribution within Antarctic waters. Microscopic algae known as diatoms are dominant members of the phytoplankton and sea ice communities, accounting for significant proportions of primary production. The overall objective of this project is to identify the molecular bases for the physiological responses of polar diatoms to varying light and iron conditions. The project should provide a means of evaluating the extent these factors regulate diatom growth and influence net community productivity in Antarctic waters. The project will also further the NSF goals of making scientific discoveries available to the general public and of training new generations of scientists. It will facilitate the teaching and learning of polar-related topics by translating the research objectives into readily accessible educational materials for middle-school students. This project will also provide funding to enable a graduate student and several undergraduate students to be trained in the techniques and perspectives of modern biology.\nAlthough numerous studies have investigated how polar diatoms are affected by varying light and iron, the cellular mechanisms leading to their distinct physiological responses remain unknown. Using comparative transcriptomics, the expression patterns of key genes and metabolic pathways in several ecologically important polar diatoms recently isolated from Antarctic waters and grown under varying iron and irradiance conditions will be examined. In addition, molecular indicators for iron and light limitation will be developed within these polar diatoms through the identification of iron- and light-responsive genes -- the expression patterns of which can be used to determine their physiological status. Upon verification in laboratory cultures, these indicators will be utilized by way of metatranscriptomic sequencing to examine iron and light limitation in natural diatom assemblages collected along environmental gradients in Western Antarctic Peninsula waters. In order to fully understand the role phytoplankton play in Southern Ocean biogeochemical cycles, dependable methods that provide a means of elucidating the physiological status of phytoplankton at any given time and location are essential. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2017-07 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Antarctica |
attribute | NC_GLOBAL | projects_0_name | String | Iron and Light Limitation in Ecologically Important Polar Diatoms: Comparative Transcriptomics and Development of Molecular Indicators |
attribute | NC_GLOBAL | projects_0_project_nid | String | 653229 |
attribute | NC_GLOBAL | projects_0_project_website | String | http://www.nsf.gov/awardsearch/showAward?AWD_ID=1341479 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2014-08 |
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 | Southernmost_Northing | double | -77.8333 |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | summary | String | BLASTp homology data from genes obtained in samples collected on the Gould (LMG1411) cruise in the Western Antarctica Peninsula during 2014 (Polar Transcriptomes project). |
attribute | NC_GLOBAL | title | String | [BLASTp homology data] - BLASTp homology data from genes obtained in samples collected on the Gould (LMG1411) cruise in the Western Antarctica Peninsula during 2014 (Polar Transcriptomes project). (Iron and Light Limitation in Ecologically Important Polar Diatoms: Comparative Transcriptomics and Development of Molecular Indicators) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | Westernmost_Easting | double | -159.4166667 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | gene | String | ||
attribute | gene | bcodmo_name | String | unknown |
attribute | gene | description | String | Gene analyzed |
attribute | gene | long_name | String | Gene |
attribute | gene | units | String | unitless |
variable | genus | String | ||
attribute | genus | bcodmo_name | String | genus |
attribute | genus | description | String | Genus analyzed |
attribute | genus | long_name | String | Genus |
attribute | genus | units | String | unitless |
variable | species | String | ||
attribute | species | bcodmo_name | String | species |
attribute | species | description | String | Species analyzed |
attribute | species | long_name | String | Species |
attribute | species | units | String | unitless |
variable | strain | String | ||
attribute | strain | bcodmo_name | String | unknown |
attribute | strain | description | String | Strain ID |
attribute | strain | long_name | String | Strain |
attribute | strain | units | String | unitless |
variable | MMETSP_ID | String | ||
attribute | MMETSP_ID | bcodmo_name | String | unknown |
attribute | MMETSP_ID | description | String | MMETSP ID |
attribute | MMETSP_ID | long_name | String | MMETSP ID |
attribute | MMETSP_ID | units | String | unitless |
variable | subject_ID | String | ||
attribute | subject_ID | bcodmo_name | String | sample |
attribute | subject_ID | description | String | Strain ID |
attribute | subject_ID | long_name | String | Subject ID |
attribute | subject_ID | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ |
attribute | subject_ID | units | String | unitless |
variable | e_value | double | ||
attribute | e_value | _FillValue | double | NaN |
attribute | e_value | actual_range | double | 0.0, 5.0E-6 |
attribute | e_value | bcodmo_name | String | unknown |
attribute | e_value | description | String | E-value |
attribute | e_value | long_name | String | E Value |
attribute | e_value | units | String | unitless |
variable | latitude | double | ||
attribute | latitude | _CoordinateAxisType | String | Lat |
attribute | latitude | _FillValue | double | NaN |
attribute | latitude | actual_range | double | -77.8333, 77.8333 |
attribute | latitude | axis | String | Y |
attribute | latitude | bcodmo_name | String | latitude |
attribute | latitude | colorBarMaximum | double | 90.0 |
attribute | latitude | colorBarMinimum | double | -90.0 |
attribute | latitude | description | String | Latitude; N is positive |
attribute | latitude | ioos_category | String | Location |
attribute | latitude | long_name | String | Latitude |
attribute | latitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LATX/ |
attribute | latitude | standard_name | String | latitude |
attribute | latitude | units | String | degrees_north |
variable | longitude | double | ||
attribute | longitude | _CoordinateAxisType | String | Lon |
attribute | longitude | _FillValue | double | NaN |
attribute | longitude | actual_range | double | -159.4166667, 163.0 |
attribute | longitude | axis | String | X |
attribute | longitude | bcodmo_name | String | longitude |
attribute | longitude | colorBarMaximum | double | 180.0 |
attribute | longitude | colorBarMinimum | double | -180.0 |
attribute | longitude | description | String | Longitude; E is positive |
attribute | longitude | ioos_category | String | Location |
attribute | longitude | long_name | String | Longitude |
attribute | longitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LONX/ |
attribute | longitude | standard_name | String | longitude |
attribute | longitude | units | String | degrees_east |
variable | clade | String | ||
attribute | clade | bcodmo_name | String | unknown |
attribute | clade | description | String | Clade category |
attribute | clade | long_name | String | Clade |
attribute | clade | units | String | unitless |