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Row Type | Variable Name | Attribute Name | Data Type | Value |
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attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv |
attribute | NC_GLOBAL | acquisition_description | String | Refer to Supplemental File, \\\"57Fe Wall Loss Experiment diagram\\\" for the\nsteps indicated in bold.\n \nAll materials were soaked overnight with heating in 1.5% Citrad Citric Acid\nliquid cleaner in deionized water, rinsed in RO water, and soaked in 10% HCl\nin Milli-Q ultrapure water for one week (due to time constraints), then rinsed\nwith MilliQ ultrapure water, let dry in an AirClean 400 work station\novernight, and double-bagged in polyethylene bags (Mellett et al., 2017). M9\nMinimal Media for bacterial cultures was made using Milli-Q ultrapure water,\ncontaining final concentrations of 33.7 mM Na\\u2082HPO\\u2084\\u00b72H\\u2082O,\n22 mM KH\\u2082PO\\u2084, 8.56 mM NaCl, 18.7 mM NH\\u2084Cl, 0.1 M magnesium\nchloride, 0.1 M calcium chloride, 2 mg/ml Thiamine HCl in 70% EtOH, and 20%\nGlucose (Kutter & Sulakvelidze, 2004). Half of the media was chelexed using\nChelex-100 resin (Pai et al., 1988) that was not acid-cleaned (C), and half\nremained un-chelexed (B). Half of each treatment was spiked with 10 \\u00b5M\nlabeled \\u2075\\u2077FeSO\\u2084(2) while half remained un-spiked (1). A volume\nof 25 ml was then filtered through either a 0.2 \\u00b5m Sterivex PVDF syringe\nfilter for the dissolved fraction (D), or a 0.02 \\u00b5m Whatman Anatop\nsyringe filter for the soluble fraction (S) (Gledhill & Buck, 2012). Samples\nwere directly filtered into trace metal clean polycarbonate Erlenmeyer flasks,\nplaced in a clean bag with a small opening to vent, and left shaking at 37\n\\u00b0C for one week. Samples of each treatment were taken initially, then\nafter the 1st, 3rd, and 7th days (t= 00, 01, 03, 07). The samples were\ndiluted, acidified, and analyzed using an ELEMENT XR High Resolution\nInductively Coupled Plasma Mass Spectrometer (HR-ICP-MS). The limit of\ndetection (LOD) for \\u2075\\u2076Fe and \\u2075\\u2077Fe were 0.3 nM and 0.012\nnM, respectively (Shrivastava & Gupta, 2011).\n \nProblem Report: \n \\u200bThe original measurements of the M9 minimal media \\u2075\\u2076Fe\ncontamination was high, so in an attempt to lower background contamination the\nmedia was chelexed. However, the Chelex-100 resin was not rinsed with acid, so\nwas less active for removal of metals. This resulted in higher than expected\nbackground concentrations of metals.\n \nThree samples were contaminated with bacterial growth (as indicated by visual\nturbidity and confirmed using SYBR nucleic acid stain and epifluorescence\nmicroscopy) over the course of the week. On t=3, sample B2 was contaminated.\nBy t=7, sample B1D and B1S were contaminated. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 713366 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1722761 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1722761 |
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 | Michael E. Sieracki |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50446 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | 57Fe Wall Loss Experiment \n PIs: Kristen Buck & Mya Breitbart (USF) \n Co-PIs: Salvatore Caprara & Chelsea Bonnain (USF) \n Verion: 04 April 2018 |
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 | 2018-04-04T17:40:41Z |
attribute | NC_GLOBAL | date_modified | String | 2020-02-11T18:33:18Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.732864.1 |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/732864 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | ICP Mass Spec |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | ELEMENT XR High Resolution Inductively Coupled Plasma Mass Spectrometer (HR-ICP-MS) |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 732867 |
attribute | NC_GLOBAL | instruments_0_description | String | An ICP Mass Spec is an instrument that passes nebulized samples into an inductively-coupled gas plasma (8-10000 K) where they are atomized and ionized. Ions of specific mass-to-charge ratios are quantified in a quadrupole mass spectrometer. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB15/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | Inductively Coupled Plasma Mass Spectrometer |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 530 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | ELEMENT XR High Resolution Inductively Coupled Plasma Mass Spectrometer |
attribute | NC_GLOBAL | keywords | String | bco, bco-dmo, biological, chelex, chemical, data, dataset, date, day, description, dmo, erddap, fe56, fe57, Fe57_SPIKE, Fe57_to_Fe56, filter, FILTER_SIZE, management, notes, oceanography, office, preliminary, sample, SAMPLE_ID, size, spike |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/732864/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/732864 |
attribute | NC_GLOBAL | param_mapping | String | {'732864': {}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/732864/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of South Florida |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | USF |
attribute | NC_GLOBAL | people_0_person_name | String | Mya Breitbart |
attribute | NC_GLOBAL | people_0_person_nid | String | 51740 |
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 South Florida |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | USF |
attribute | NC_GLOBAL | people_1_person_name | String | Kristen N. Buck |
attribute | NC_GLOBAL | people_1_person_nid | String | 51624 |
attribute | NC_GLOBAL | people_1_role | String | Principal Investigator |
attribute | NC_GLOBAL | people_1_role_type | String | originator |
attribute | NC_GLOBAL | people_2_affiliation | String | University of South Florida |
attribute | NC_GLOBAL | people_2_affiliation_acronym | String | USF |
attribute | NC_GLOBAL | people_2_person_name | String | Chelsea Bonnain |
attribute | NC_GLOBAL | people_2_person_nid | String | 732872 |
attribute | NC_GLOBAL | people_2_role | String | Co-Principal Investigator |
attribute | NC_GLOBAL | people_2_role_type | String | originator |
attribute | NC_GLOBAL | people_3_affiliation | String | University of South Florida |
attribute | NC_GLOBAL | people_3_affiliation_acronym | String | USF |
attribute | NC_GLOBAL | people_3_person_name | String | Salvatore Caprara |
attribute | NC_GLOBAL | people_3_person_nid | String | 732874 |
attribute | NC_GLOBAL | people_3_role | String | Co-Principal Investigator |
attribute | NC_GLOBAL | people_3_role_type | String | originator |
attribute | NC_GLOBAL | people_4_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_4_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_4_person_name | String | Shannon Rauch |
attribute | NC_GLOBAL | people_4_person_nid | String | 51498 |
attribute | NC_GLOBAL | people_4_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_4_role_type | String | related |
attribute | NC_GLOBAL | project | String | Fe-Virus |
attribute | NC_GLOBAL | projects_0_acronym | String | Fe-Virus |
attribute | NC_GLOBAL | projects_0_description | String | Iron is an essential micronutrient for phytoplankton that is required for photosynthesis and respiration. Insufficient iron has been shown to limit phytoplankton growth in large regions of the surface ocean, and correspondingly, iron cycling is directly linked to carbon cycling in much of the marine environment. Nearly all iron in seawater (>99%) exists as complexes with organic molecules called ligands, which govern the concentration of iron dissolved in the water and the bioavailability of that iron to phytoplankton. However, despite the importance of iron-binding organic ligands, their sources and identities are largely unknown. Viruses, the majority of which are phages (viruses that infect bacteria), are extremely abundant in seawater and are in the same size fraction as dissolved iron. Recent evidence that non-marine phages contain iron as part of their structures has led to the proposal that marine phages may represent a previously overlooked class of organic iron-binding ligands. This project is determining the contribution of marine phages to dissolved iron pools and culture phage-host systems in the laboratory to determine if phages utilize bacterial iron-uptake receptors for infection in the manner of a Trojan horse. As the first study to examine the biogeochemical impact of trace elements contained within the structure of highly abundant marine phage particles, successful completion of the proposed research will be transformative for biological and chemical oceanography and have far-reaching implications for other fields, including human health where iron availability plays an important role in microbial pathogenesis. This project contributes to the multidisciplinary training of a graduate student and postdoctoral researcher. Research results will be disseminated through scientific publications and presentations, and the public will be educated about linkages between viruses and ocean chemistry via a hands-on exhibit for the annual St. Petersburg Science Festival.\nBuilding upon evidence from non-marine model systems demonstrating the presence of iron ions in phage tail proteins and phage utilization of cell surface receptors for siderophore-bound iron, this project combines field and laboratory-based experiments to test the following three hypotheses regarding iron-virus interactions in the oceans: (1) Iron incorporated into phage tails originates from bacterial cell reserves, reducing the amount of iron available for remineralization upon lysis; (2) Phages constitute important iron-binding ligands in the oceans, accounting for a substantial portion of organically complexed colloidal dissolved iron; (3) Marine phages compete with siderophore-bound iron for uptake receptors on the bacterial cell surface and use iron in their tails as a Trojan horse for infection. Initial calculations predict that phages could account for up to 70% of the colloidal fraction of organically complexed dissolved iron in the surface ocean; therefore, this project is critical for advancing knowledge of trace-metal cycling as well as phage-host interactions. Additionally, if a portion of the cellular iron thought to be released from bacterial cells for remineralization following lysis is already incorporated into phage tails, then these findings will have significant implications for oceanic biogeochemical models. Through a combination of laboratory-based culture experiments and field sample measurements, this project could reveal the identity of a ubiquitous component of colloidal organic iron-binding ligands, modify the estimates of iron concentrations and species released through viral lysis, and potentially identify a novel receptor type for marine phage that may compete with the acquisition of siderophore-bound iron by host bacteria. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2019-01 |
attribute | NC_GLOBAL | projects_0_name | String | EAGER: Iron-Virus Interactions in the Ocean |
attribute | NC_GLOBAL | projects_0_project_nid | String | 713367 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2017-02 |
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 | DATE |
attribute | NC_GLOBAL | summary | String | This data was collected as part of a method development study investigating the precipitation and wall loss of labeled \\u2075\\u2077Fe when added to M9 Minimal Media, which is used to grow the model bacterial species Escherichia coli. The bulk media was prepared with the same components and a portion was treated with Chelex-100 to remove metals, while the other portion remained un-chelexed. Half of each treatment was spiked with labeled \\u2075\\u2077Fe and either 0.2 \\u03bcm or 0.02 \\u03bcm filtered for comparison of the dissolved and soluble fractions. The \\u2075\\u2077Fe content was monitored over four time points for one week in a shaking incubator, under the same conditions used to culture E. coli for labeling experiments. |
attribute | NC_GLOBAL | title | String | [57Fe Wall Loss Experiment] - 57Fe Wall Loss Experiment data collected as part of a method development study investigating the precipitation and wall loss of labeled 57Fe when added to M9 Minimal Media (EAGER: Iron-Virus Interactions in the Ocean) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | DATE | int | ||
attribute | DATE | _FillValue | int | 2147483647 |
attribute | DATE | actual_range | int | 20171113, 20171113 |
attribute | DATE | bcodmo_name | String | date |
attribute | DATE | description | String | Date (UTC) when media was filtered and experiment initiated (t=0), in format YYYYMMDD |
attribute | DATE | long_name | String | DATE |
attribute | DATE | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P01/current/ADATAA01/ |
attribute | DATE | units | String | unitless |
variable | SAMPLE_ID | String | ||
attribute | SAMPLE_ID | bcodmo_name | String | sample |
attribute | SAMPLE_ID | description | String | Sample identifier designated B for un-chelexed, or C for chelexed; 1 for un-spiked with 57FeSO4, 2 for spiked with 10 uM 57FeSO4; D for dissolved (0.2 um filtered) or S for soluble (0.02 um filtered) |
attribute | SAMPLE_ID | long_name | String | SAMPLE ID |
attribute | SAMPLE_ID | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ |
attribute | SAMPLE_ID | units | String | unitless |
variable | DESCRIPTION | String | ||
attribute | DESCRIPTION | bcodmo_name | String | treatment |
attribute | DESCRIPTION | description | String | Description of treatment type |
attribute | DESCRIPTION | long_name | String | DESCRIPTION |
attribute | DESCRIPTION | units | String | unitless |
variable | CHELEX | String | ||
attribute | CHELEX | bcodmo_name | String | treatment |
attribute | CHELEX | description | String | Solution was treated with Chelex-100 resin (Yes) or not (No), units in Yes/No |
attribute | CHELEX | long_name | String | CHELEX |
attribute | CHELEX | units | String | unitless |
variable | Fe57_SPIKE | byte | ||
attribute | Fe57_SPIKE | _FillValue | byte | 127 |
attribute | Fe57_SPIKE | actual_range | byte | 0, 10 |
attribute | Fe57_SPIKE | bcodmo_name | String | treatment |
attribute | Fe57_SPIKE | description | String | 57FeSO4 spike concentration as added to the media |
attribute | Fe57_SPIKE | long_name | String | Fe57 SPIKE |
attribute | Fe57_SPIKE | units | String | micromolar (uM) |
variable | FILTER_SIZE | String | ||
attribute | FILTER_SIZE | bcodmo_name | String | filter_size |
attribute | FILTER_SIZE | description | String | Pore size used to filter media, using 0.2 um Sterivex PVDF syringe filter or 0.02 um Anatop syringe filter |
attribute | FILTER_SIZE | long_name | String | FILTER SIZE |
attribute | FILTER_SIZE | units | String | micrometers (um) |
variable | DAY | byte | ||
attribute | DAY | _FillValue | byte | 127 |
attribute | DAY | actual_range | byte | 0, 7 |
attribute | DAY | bcodmo_name | String | days |
attribute | DAY | description | String | Time when treatment was sampled, t=n, units in days |
attribute | DAY | long_name | String | DAY |
attribute | DAY | units | String | days |
variable | Fe56 | float | ||
attribute | Fe56 | _FillValue | float | NaN |
attribute | Fe56 | actual_range | float | 10.73, 738.92 |
attribute | Fe56 | bcodmo_name | String | Fe |
attribute | Fe56 | description | String | Concentration of 56Fe as determined by HR-ICP-MS |
attribute | Fe56 | long_name | String | Fe56 |
attribute | Fe56 | units | String | nanomolar (nM) |
variable | Fe57 | float | ||
attribute | Fe57 | _FillValue | float | NaN |
attribute | Fe57 | actual_range | float | 2.13, 10857.82 |
attribute | Fe57 | bcodmo_name | String | Fe |
attribute | Fe57 | description | String | Concentration of 57Fe as determined by HR-ICP-MS |
attribute | Fe57 | long_name | String | Fe57 |
attribute | Fe57 | units | String | nanomolar (nM) |
variable | Fe57_to_Fe56 | float | ||
attribute | Fe57_to_Fe56 | _FillValue | float | NaN |
attribute | Fe57_to_Fe56 | actual_range | float | 2.27, 2459.01 |
attribute | Fe57_to_Fe56 | bcodmo_name | String | Fe |
attribute | Fe57_to_Fe56 | description | String | Ratio of 57Fe concentration to 56Fe concentration as measured by the HR-ICP-MS, multiplied by 100 (in percentage) |
attribute | Fe57_to_Fe56 | long_name | String | Fe57 To Fe56 |
attribute | Fe57_to_Fe56 | units | String | unitless (percentage) |
variable | NOTES | String | ||
attribute | NOTES | bcodmo_name | String | comment |
attribute | NOTES | description | String | Some samples contaminated by bacterial growth were designated as such |
attribute | NOTES | long_name | String | NOTES |
attribute | NOTES | units | String | unitless |