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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 | Cultures:\\u00a0Pleurochrysis carterae\\u00a0cultures were maintained in\nexponential growth phase under axenic conditions in semi-continuous batch\nculture using L1-Si media prepared on 0.2 um-filtered, UV-sterilized,\nautoclaved seawater.\\u00a0 Cultures were acclimated to one of\nthree\\u00a0pCO2\\u00a0treatments for > 9 generations before experiments were\nperformed.\\u00a0 Cultures were maintained in an incubator at 16.5 +/- 0.5 deg\nC and 470 umol photons/m-2/s\\u00a0PAR.\n \npCO2: Carbonate chemistry was manipulated by bubbling cultures and prepared\nmedia with 500 mL/min\\u00a0with 0.2 um-filtered 280, 380, or 750\nppm\\u00a0pCO2\\u00a0air.\\u00a0 The\\u00a0pCO2\\u00a0levels of the treatment air\nwere established using two mass flow controllers (Aalborg, Orangeburg, NY,\nUSA) for each treatment to precisely mix in-house compressed air and pure\nCO2\\u00a0(Maine Oxy, Auburn, ME, USA).\\u00a0 The in-house compressed air was\nstripped of CO2\\u00a0to less than 10 ppm CO2\\u00a0using a Puregas VCD\nCO2\\u00a0Adsorber (Puregas, LLC, Broomfield, CO, USA).\\u00a0\nThe\\u00a0pCO2\\u00a0of the gas mixtures was stable to +/- 8\nppm.\\u00a0\\u00a0pCO2\\u00a0values of the cultures may be different than the\ntarget levels due to biological activity.\n \nDissolution of existing coccoliths:\\u00a0 Coccoliths were dissolved by 1.75 M\nHCl to drop the pH to 5.5 for 2 min.\\u00a0 Following the dissolution (de-\nlithing), 1.75 M NaOH was added to bring the pH back to the respective\nstarting pH.\\u00a0 Dissolution of coccoliths was immediately confirmed by\nlooking at the cells under cross-polarized light microscopy to verify the\nabsence of birefringence indicative of CaCO3.\\u00a0 Dissolution was further\nconfirmed by filtering the acidified/neutralized sample onto a 0.4 um\npolycarbonate filter.\\u00a0 Filters were mounted on stubs, sputter-coated with\ngold using a Denton Desk IV sputter coater (Denton Vacuum, Moorestown, NJ,\nUSA), and imaged on a Zeiss Supra25 field emission scanning electron\nmicroscope (Carl Zeiss Microscopy, LLC, Thornwood, NY, USA).\\u00a0 At least 15\ncells per sample were imaged and the number of coccoliths/cell\\u00a0was\nmanually counted to determine the number of coccoliths that remained after the\nacidification/neutralization dissolution step.\n \n24 h incubation in either light or dark conditions:\\u00a0 To determine the\nnumber of coccoliths formed (as a proxy for calcification rate) in 24 h in\neither light or dark conditions, for each\\u00a0pCO2\\u00a0level, 15 mL of de-\nlithed culture were added to 8 scintillation vials.\\u00a0 Three vials were\n\\u2018light\\u2019 replicates, three vials were \\u2018dark\\u2019 replicates,\nand two vials were poisoned with buffered formalin to serve as a\n\\u2018light\\u2019 blank and a \\u2018dark\\u2019 blank.\\u00a0 Dark replicate and\nblank vials were covered in black aluminum foil and all vials were incubated\ntogether for 24 h in an incubator set at 16.5 +/- 0.5 deg C and 470 umol\nphotons/m-2/s\\u00a0PAR on a 14-10 h light-dark cycle.\\u00a0The experiment was\ntimed to start when the lights in the incubator turned on in the morning, thus\nthe \\u2018light\\u2019 replicates were exposed to light for 14 of 24 h.\\u00a0\n \nDetermination of attached coccoliths:\\u00a0\\u00a0Coccolith formation was\nassessed by counting the number of coccoliths formed during the incubation\nperiod.\\u00a0 After the 24 h incubation period, each replicate and blank vial\nwas filtered onto a 0.4 um polycarbonate filters.\\u00a0 Filters were mounted\non stubs, sputter-coated with gold using a Denton Desk IV sputter coater\n(Denton Vacuum, Moorestown, NJ, USA), and imaged on a Zeiss Supra25 field\nemission SEM (Carl Zeiss Microscopy, LLC, Thornwood, NY, USA).\\u00a0 At least\n15 cells per replicate were imaged and the number of coccoliths/cell\\u00a0was\nmanually counted.\\u00a0 The counted coccoliths represented calcification\nduring the 24 h incubation period and the average number of coccoliths per\ncell for each replicate and blank is reported. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 514411 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1220068 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://nsf.gov/awardsearch/showAward?AWD_ID=1220068 |
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 | Light-Dark Calcification \n W. Balch and D. Fields, PIs \n Version 4 November 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 | 2016-11-04T21:25:51Z |
attribute | NC_GLOBAL | date_modified | String | 2019-04-18T15:55:03Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.664013.1 |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/664013 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | in-situ incubator |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | Dark replicate and blank vials were covered in black aluminum foil and all vials were incubated together for 24 h in an incubator set at 16.5 +/- 0.5 deg C and 470 umol photons/m-2/s PAR on a 14-10 h light-dark cycle. |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 664040 |
attribute | NC_GLOBAL | instruments_0_description | String | A device on shipboard or in the laboratory that holds water samples under controlled conditions of temperature and possibly illumination. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/82/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | In-situ incubator |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 494 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | Incubator |
attribute | NC_GLOBAL | instruments_1_acronym | String | pH Sensor |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_description | String | Orion ROSS electrode was connected to an Orion Star A211 Benchtop pH meter (ThermoFisher Scientific, Waltham, MA, USA) |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_nid | String | 664025 |
attribute | NC_GLOBAL | instruments_1_description | String | General term for an instrument that measures the pH or how acidic or basic a solution is. |
attribute | NC_GLOBAL | instruments_1_instrument_name | String | pH Sensor |
attribute | NC_GLOBAL | instruments_1_instrument_nid | String | 674 |
attribute | NC_GLOBAL | instruments_1_supplied_name | String | Orion ROSS electrode |
attribute | NC_GLOBAL | instruments_2_dataset_instrument_description | String | Carl Zeiss Microscopy, LLC, Thornwood, NY, USA |
attribute | NC_GLOBAL | instruments_2_dataset_instrument_nid | String | 664039 |
attribute | NC_GLOBAL | instruments_2_description | String | Instruments that generate enlarged images of samples using the phenomena of reflection and absorption of electrons behaving as waves. |
attribute | NC_GLOBAL | instruments_2_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB07/ |
attribute | NC_GLOBAL | instruments_2_instrument_name | String | Microscope-Electron |
attribute | NC_GLOBAL | instruments_2_instrument_nid | String | 709 |
attribute | NC_GLOBAL | instruments_2_supplied_name | String | Zeiss Supra25 field emission SEM |
attribute | NC_GLOBAL | instruments_3_acronym | String | MFC |
attribute | NC_GLOBAL | instruments_3_dataset_instrument_description | String | Indicate and control set flow rates of gases. Manufactured in Orangeburg, NY USA. |
attribute | NC_GLOBAL | instruments_3_dataset_instrument_nid | String | 664022 |
attribute | NC_GLOBAL | instruments_3_description | String | Mass Flow Controller (MFC) - A device used to measure and control the flow of fluids and gases |
attribute | NC_GLOBAL | instruments_3_instrument_name | String | Mass Flow Controller |
attribute | NC_GLOBAL | instruments_3_instrument_nid | String | 712 |
attribute | NC_GLOBAL | instruments_3_supplied_name | String | Aalborg Mass Flow Controller |
attribute | NC_GLOBAL | instruments_4_acronym | String | CO2 Adsorber |
attribute | NC_GLOBAL | instruments_4_dataset_instrument_description | String | Instrument stripped compressed air of CO2 |
attribute | NC_GLOBAL | instruments_4_dataset_instrument_nid | String | 664023 |
attribute | NC_GLOBAL | instruments_4_description | String | CO2 Adsorber - an instrument designed to remove CO2 and moisture from compressed air. |
attribute | NC_GLOBAL | instruments_4_instrument_name | String | CO2 Adsorber |
attribute | NC_GLOBAL | instruments_4_instrument_nid | String | 651526 |
attribute | NC_GLOBAL | instruments_4_supplied_name | String | Puregas VCD CO2 Adsorber |
attribute | NC_GLOBAL | instruments_5_acronym | String | Sputter Coater |
attribute | NC_GLOBAL | instruments_5_dataset_instrument_description | String | Filters were mounted on stubs, sputter-coated with gold using a Denton Desk IV sputter coater (Denton Vacuum, Moorestown, NJ, USA). |
attribute | NC_GLOBAL | instruments_5_dataset_instrument_nid | String | 664042 |
attribute | NC_GLOBAL | instruments_5_description | String | Sputter coating is the standard method for preparing non-conducting or poorly conducting specimens prior to observation in a scanning electron microscope (SEM) |
attribute | NC_GLOBAL | instruments_5_instrument_name | String | Sputter Coater |
attribute | NC_GLOBAL | instruments_5_instrument_nid | String | 664041 |
attribute | NC_GLOBAL | instruments_5_supplied_name | String | Denton Desk IV sputter coater |
attribute | NC_GLOBAL | keywords | String | attached, attached_blankCorrected, bco, bco-dmo, biological, blank, carbon, carbon dioxide, chemical, co2, conditions, corrected, data, dataset, deviation, dioxide, dmo, erddap, light, light_conditions, management, mean, mean_attached_blankCorrected, oceanography, office, pCO2_treatment, preliminary, sample, standard, standard deviation, stdev, stdev_attached_blankCorrected, treatment |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/664013/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/664013 |
attribute | NC_GLOBAL | param_mapping | String | {'664013': {}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/664013/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | Bigelow Laboratory for Ocean Sciences |
attribute | NC_GLOBAL | people_0_person_name | String | William M. Balch |
attribute | NC_GLOBAL | people_0_person_nid | String | 50650 |
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 | Bigelow Laboratory for Ocean Sciences |
attribute | NC_GLOBAL | people_1_person_name | String | David Fields |
attribute | NC_GLOBAL | people_1_person_nid | String | 51141 |
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 | Bigelow Laboratory for Ocean Sciences |
attribute | NC_GLOBAL | people_2_person_name | String | William M. Balch |
attribute | NC_GLOBAL | people_2_person_nid | String | 50650 |
attribute | NC_GLOBAL | people_2_role | String | Contact |
attribute | NC_GLOBAL | people_2_role_type | String | related |
attribute | NC_GLOBAL | people_3_affiliation | String | Bigelow Laboratory for Ocean Sciences |
attribute | NC_GLOBAL | people_3_person_name | String | Meredith White |
attribute | NC_GLOBAL | people_3_person_nid | String | 514420 |
attribute | NC_GLOBAL | people_3_role | String | Contact |
attribute | NC_GLOBAL | people_3_role_type | String | related |
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 | Hannah Ake |
attribute | NC_GLOBAL | people_4_person_nid | String | 650173 |
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 | OA_Copes_Coccoliths |
attribute | NC_GLOBAL | projects_0_acronym | String | OA_Copes_Coccoliths |
attribute | NC_GLOBAL | projects_0_description | String | (Extracted from the NSF award abstract)\nOcean acidification is one of the most pressing marine science issues of our time, with potential biological impacts spanning all marine phyla and potential societal impacts affecting man's relationship to the sea. Rising levels of atmospheric pCO2 are increasing the acidity of the world oceans. It is generally held that average surface ocean pH has already declined by 0.1 pH units relative to the pre-industrial level (Orr et al., 2005), and is projected to decrease 0.3 to 0.46 units by the end of this century, depending on CO2 emission scenarios (Caldeira and Wickett, 2005). The overall goal of this research is to parameterize how changes in pCO2 levels could alter the biological and alkalinity pumps of the world ocean. Specifically, the direct and indirect effects of ocean acidification will be examined within a simple, controlled predator/prey system containing a single prey phytoplankton species (the coccolithophore, Emiliania huxleyi) and a single predator (the oceanic metazoan grazer, Calanus finmarchicus). The experiments are designed to elucidate both direct effects (i.e. effects of ocean acidification on the individual organisms only) and interactive effects (i.e. effects on the combined predator/prey system). Interactive experiments with phytoplankton prey and zooplankton predator are a critical starting point for predicting the overall impact of ocean acidification in marine ecosystems. To meet these goals, a state-of-the-art facility will be constructed with growth chambers that are calibrated and have highly-controlled pH and alkalinity levels. The strength of this approach lies in meticulous calibration and redundant measurements that will be made to ensure that conditions within the chambers are well described and tightly monitored for DIC levels. Growth and calcification rates in coccolithophores and the developmental rates, morphological and behavioral effects on copepods will be measured. The PIC and POC in the algae and the excreted fecal pellets will be monitored for changes in the PIC/POC ratio, a key parameter for modeling feedback mechanisms for rising pCO2 levels. In addition, 14C experiments are planned to measure calcification rates in coccolithophores and dissolution rates as a result of grazing. These key experiments will verify closure in the mass balance of PIC, allowing the determination of actual dissolution rates of PIC within the guts of copepod grazers. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2015-07 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Laboratory experiments; East Boothbay, Maine |
attribute | NC_GLOBAL | projects_0_name | String | Effects of ocean acidification on Emiliania huxleyi and Calanus finmarchicus; insights into the oceanic alkalinity and biological carbon pumps |
attribute | NC_GLOBAL | projects_0_project_nid | String | 514415 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2012-08 |
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 | summary | String | Light-dark calcification rates of Pleurochrysis carterae analyzed at Bigelow Laboratory in 2013 (OA Copes Coccoliths project) |
attribute | NC_GLOBAL | title | String | [Pleurochrysis carterae light-dark calcification] - Light-dark calcification rates of Pleurochrysis carterae analyzed at Bigelow Laboratory in 2013 (OA Copes Coccoliths project) (Effects of ocean acidification on Emiliania huxleyi and Calanus finmarchicus; insights into the oceanic alkalinity and biological carbon pumps) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | pCO2_treatment | short | ||
attribute | pCO2_treatment | _FillValue | short | 32767 |
attribute | pCO2_treatment | actual_range | short | 280, 750 |
attribute | pCO2_treatment | bcodmo_name | String | treatment |
attribute | pCO2_treatment | description | String | The independent variable - one of three pCO2 levels (280 ppm, 380 ppm, or 750 ppm) These treatment levels are nominal values as they represent the target pCO2 for each treatment. |
attribute | pCO2_treatment | long_name | String | P CO2 Treatment |
attribute | pCO2_treatment | units | String | parts per million (ppm) |
variable | sample | String | ||
attribute | sample | bcodmo_name | String | sample |
attribute | sample | description | String | For each pCO2 treatment there are three types of samples;\nAfter de-lithing: These samples were taken immediately after the coccolithophores were acidified to dissolve their coccoliths and then neutralized to return the culture pH to the original pH. These samples were taken before the 24 h incubation period and therefore do not have a Light or Dark treatment.\nReplicate: These represent the three replicates for each light condition and each CO2 treatment. These samples were taken after the cells incubated in either light or dark conditions for 24 h.\nBlank: These samples were killed by the addition of formalin but were allowed to incubate in either light or dark conditions for 24 h. |
attribute | sample | long_name | String | Sample |
attribute | sample | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ |
attribute | sample | units | String | unitless |
variable | light_conditions | String | ||
attribute | light_conditions | bcodmo_name | String | PAR |
attribute | light_conditions | description | String | This identifies whether the sample was incubated for 24 h in light (470 umol photons/m-2/s PAR) or dark (0 umol photons/m-2/s PAR) conditions. |
attribute | light_conditions | long_name | String | Light Conditions |
attribute | light_conditions | units | String | unitless |
variable | attached | float | ||
attribute | attached | _FillValue | float | NaN |
attribute | attached | actual_range | float | 0.0, 33.0 |
attribute | attached | bcodmo_name | String | cell_concentration |
attribute | attached | description | String | This is the number of attached coccoliths observed per cell. This number represents an average of counts from at least 15 cells per replicate or sample. |
attribute | attached | long_name | String | Attached |
attribute | attached | units | String | coccoliths per cell |
variable | attached_blankCorrected | float | ||
attribute | attached_blankCorrected | _FillValue | float | NaN |
attribute | attached_blankCorrected | actual_range | float | 0.0, 32.8 |
attribute | attached_blankCorrected | bcodmo_name | String | cell_concentration |
attribute | attached_blankCorrected | description | String | This is the number of attached coccoliths observed per cell with the number of coccoliths observed per cell from the blank samples subtracted to account for any coccoliths that might have remained after cells were de-lithed. |
attribute | attached_blankCorrected | long_name | String | Attached Blank Corrected |
attribute | attached_blankCorrected | units | String | coccoliths per cell |
variable | mean_attached_blankCorrected | float | ||
attribute | mean_attached_blankCorrected | _FillValue | float | NaN |
attribute | mean_attached_blankCorrected | actual_range | float | 0.21, 30.72 |
attribute | mean_attached_blankCorrected | bcodmo_name | String | mean |
attribute | mean_attached_blankCorrected | description | String | The average value for each set of three replicates. |
attribute | mean_attached_blankCorrected | long_name | String | Mean Attached Blank Corrected |
attribute | mean_attached_blankCorrected | units | String | coccoliths per cell |
variable | stdev_attached_blankCorrected | float | ||
attribute | stdev_attached_blankCorrected | _FillValue | float | NaN |
attribute | stdev_attached_blankCorrected | actual_range | float | 0.37, 2.75 |
attribute | stdev_attached_blankCorrected | bcodmo_name | String | standard deviation |
attribute | stdev_attached_blankCorrected | description | String | The standard deviation for each set of three replicates. |
attribute | stdev_attached_blankCorrected | long_name | String | Stdev Attached Blank Corrected |
attribute | stdev_attached_blankCorrected | units | String | coccoliths per cell |