The Data Access Portal has information in 3 columns. An outline of the content in these columns is provided above. When first entering the search interface, all potential datasets are listed. Datasets are indicated in the map and results tabulation elements which are located in the middle column. The order of results can be modified using the "Sort by" option in the left column. On top of this column is normally relevant guidance information to user presented as collapsible elements.
If the user want to refine the search, this can be done by constraining the bounding box search. This is done in the map - the listing of datasets is automatically updated. Date constraints can be added in the left column. For these to take effect, the user has to push the button marked search. In the left column it is also possible to specific text elements to search for in the datasets. Again pushing the button marked "Search" is necessary for these to take action. Complex search patterns can be constructed using logical operators and phrases embedded in quotation marks. Logical operators include AND, OR and NOT. Remember to add space around operators. Text strings that are not quoted are trated as separate words and will match any of the words (i.e. assuming the OR operator). E.g. in order to find WMO synoptic weather station data from Verlegenhuken use the search phrase: [synop AND verlegenhuken]. Searches are case insensitive.
Other elements indicated in the left and right columns are facet searches, i.e. these are keywords that are found in the datasets and all datasets that contain these specific keywords in the appropriate metadata elements are listed together. Further refinement can be done using full text, date or bounding box constraints. Individuals, organisations and data centres involved in generating or curating the datasets are listed in the facets in the right column.
Collections
Collections allows the user to search in subsets of the existing catalogue. The collections are primarily data management projects that have been incorporated in the ADC catalogue after the project has ended. In this context the ADC is the long term access solution for these data. The collections currently served through ADC include (datasets may belong to multiple data collections):
ADC is the full collection of this service CC is the CryoClim collection
In order to search a specific data collection select that collection. If no data collection is selected all collections are searched.
AeN are data related to the Nansen Legacy project and are better explored through the SIOS Data Access Point using the collection defined there which is available through this URL.
SIOS, InfraNOR, SIOSCD, SIOSAP, SESS_* are collections related to SIOS. These are better explored through the SIOS Data Access Portal
Some cleaning is pending between InfraNOR and SIOSIN, for some of the SESS collections.
Citation of data and service
Always remember to cite data when used!
Citation information for individual datasets is often provided in the metadata. However, not all datasets have this information embedded in the discovery metadata. On a general basis a citation of a dataset include the same components as any other citation:
author,
title,
year of publication,
publisher (for data this is often the archive where it is housed),
edition or version,
access information (a URL or persistent identifier, e.g. DOI if provided)
The information required to properly cite a dataset is normally provided in the discovery metadata the datasets.
If you use data retrieved through this portal, please acknowledge the Norwegian Meteorological Institute/Arctic Data Centre.
The Hive Wireless sensor network project designed and assembled automatic weather stations that are currently installed at Kongsvegen glacier in Svalbard and records near surface meteorological variables: air temperature, relative humidity, air pressure, snow height, wind, surface skin temperature... The HiveWSN kit consists of: 1) a brain box containing the power system, the microcontroller, the communication system and the connectivity to the sensors, 2) A set of sensors either commercially available or custom built at the Department of Geosciences at UiO as part of the UiO Hive project. The kit is autonomous and packaged as a beam that can be installed on simple mast. Currently, there are two versions of the WSN system: v1 from 2019, and v2 from 2021. Both are based on the board Wasmpote v15 which handle power, communication, and data brokerage. The firmware running all instances has been written as part of the project UiO Hive, and include a set of tools described on the HiveWSN project website: https://www.mn.uio.no/geo/english/research/projects/hive. Important note: the height of the sensor to the snow/ice surface is not corrected for variations in surface deposition or melt over time. The sensor box is fixed to a stake drilled into the snow/ice.
The Hive Wireless sensor network project designed and assembled automatic weather stations that are currently installed at Kongsvegen glacier in Svalbard and records near surface meteorological variables: air temperature, relative humidity, air pressure, snow height, wind, surface skin temperature... The HiveWSN kit consists of: 1) a brain box containing the power system, the microcontroller, the communication system and the connectivity to the sensors, 2) A set of sensors either commercially available or custom built at the Department of Geosciences at UiO as part of the UiO Hive project. The kit is autonomous and packaged as a beam that can be installed on simple mast. Currently, there are two versions of the WSN system: v1 from 2019, and v2 from 2021. Both are based on the board Wasmpote v15 which handle power, communication, and data brokerage. The firmware running all instances has been written as part of the project UiO Hive, and include a set of tools described on the HiveWSN project website: https://www.mn.uio.no/geo/english/research/projects/hive. Important note: the height of the sensor to the snow/ice surface is not corrected for variations in surface deposition or melt over time. The sensor box is fixed to a stake drilled into the snow/ice.
The Hive Wireless sensor network project designed and assembled automatic weather stations that are currently installed at Kongsvegen glacier in Svalbard and records near surface meteorological variables: air temperature, relative humidity, air pressure, snow height, wind, surface skin temperature... The HiveWSN kit consists of: 1) a brain box containing the power system, the microcontroller, the communication system and the connectivity to the sensors, 2) A set of sensors either commercially available or custom built at the Department of Geosciences at UiO as part of the UiO Hive project. The kit is autonomous and packaged as a beam that can be installed on simple mast. Currently, there are two versions of the WSN system: v1 from 2019, and v2 from 2021. Both are based on the board Wasmpote v15 which handle power, communication, and data brokerage. The firmware running all instances has been written as part of the project UiO Hive, and include a set of tools described on the HiveWSN project website: https://www.mn.uio.no/geo/english/research/projects/hive. Important note: the height of the sensor to the snow/ice surface is not corrected for variations in surface deposition or melt over time. The sensor box is fixed to a stake drilled into the snow/ice.
The Hive Wireless sensor network project designed and assembled automatic weather stations that are currently installed at Kongsvegen glacier in Svalbard and records near surface meteorological variables: air temperature, relative humidity, air pressure, snow height, wind, surface skin temperature... The HiveWSN kit consists of: 1) a brain box containing the power system, the microcontroller, the communication system and the connectivity to the sensors, 2) A set of sensors either commercially available or custom built at the Department of Geosciences at UiO as part of the UiO Hive project. The kit is autonomous and packaged as a beam that can be installed on simple mast. Currently, there are two versions of the WSN system: v1 from 2019, and v2 from 2021. Both are based on the board Wasmpote v15 which handle power, communication, and data brokerage. The firmware running all instances has been written as part of the project UiO Hive, and include a set of tools described on the HiveWSN project website: https://www.mn.uio.no/geo/english/research/projects/hive. Important note: the height of the sensor to the snow/ice surface is not corrected for variations in surface deposition or melt over time. The sensor box is fixed to a stake drilled into the snow/ice.
The Hive Wireless sensor network project designed and assembled automatic weather stations that are currently installed at Kongsvegen glacier in Svalbard and records near surface meteorological variables: air temperature, relative humidity, air pressure, snow height, wind, surface skin temperature... The HiveWSN kit consists of: 1) a brain box containing the power system, the microcontroller, the communication system and the connectivity to the sensors, 2) A set of sensors either commercially available or custom built at the Department of Geosciences at UiO as part of the UiO Hive project. The kit is autonomous and packaged as a beam that can be installed on simple mast. Currently, there are two versions of the WSN system: v1 from 2019, and v2 from 2021. Both are based on the board Wasmpote v15 which handle power, communication, and data brokerage. The firmware running all instances has been written as part of the project UiO Hive, and include a set of tools described on the HiveWSN project website: https://www.mn.uio.no/geo/english/research/projects/hive. Important note: the height of the sensor to the snow/ice surface is not corrected for variations in surface deposition or melt over time. The sensor box is fixed to a stake drilled into the snow/ice.
The data has been collected during the Nansen Legacy Joint Cruise 3, 19th February – 11th March 2022 on the research vessel RV Kronprins Haakon (cruise number 2022702), along a transect from 76N to 82N east of Svalbard. The dataset contains mesozooplankton occurrence. It has been sampled using a BongoNet, HydroBios 60 cm. Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton with a mesh-size 180 µm. All specimens are identified to the lowest taxonomical level and the occurrence is given for a specific species and stage or size group as ind/m3.
Sampling method:
The sampling covers a transect from 76 N to 82 N in the northern Barents Sea and Arctic Ocean. Zooplankton has been collected using a BongoNet 60 cm (HydroBios, opening: 0.2827 m2, net length: 250 cm). Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton with a mesh-size 180 µm. All samples were added 4 % formaldehyde free from acid.
PLEASE NOTE: THIS DATASET CONTAINS TWO COMPLETE DATASETS OF ZOOPLANKTON: ONE FOR SMALL MESOZOOPLANKTON (APPROX BODY SIZE BELOW 2 MM) COLLECTED WITH MULTINET 64 µM AND ONE FOR LARGE MESOZOOPLANKTON (APPROX BODY SIZE ABOVE 2 MM) COLLECTED WITH MULTINET 180 µM MESH SIZE. THE INFO ABOUT WHICH NET IS USED CAN BE FOUND IN gearType, USE EITHER 64 UM OR 180 UM DEPENDING ON WHETHER THE FOCUS IS SMALL OR LARGE MESOZOOPLANKTON
Analyse method:
All samples have been analysed at Institute of Oceanology of the Polish Academy of Sciences (IOPAN). The organisms were identified and counted under a stereomicroscope equipped with an ocular micrometer, according to standard procedures (Harris et al. 2000). Small-sized zooplankters (most of Copepoda, juvenile stages of Pteropoda, Euphausiacea, Ostracoda, Amphipoda and Chaetognatha) were identified and counted in sub-samples obtained from the fixed sample volume by automatic pipette (approximately 500 individuals). Large zooplankters (big Copepoda, Pteropoda, Euphausiacea, Ostracoda, Amphipoda, Decapoda, Appendicularia, Chaetognatha, and Pisces larvae) were sorted out and identified from the whole sample. Representatives of Calanus spp. were identified at the species level based on morphology and prosome lengths of individual copepodid stages (Kwasniewski et al. 2003).
Data structure:
The data is following Darwin Core nomenclature as far as possible but also include variables that aren’t supported by Darwin Core. All information about the sampling such as eventDate, latitude, longitude, depts etc is located in event file while the result such as scientificName, lifeStage, occurrence etc. are found in the occurrence file
Header name index - events
- expedition: cruise number for R/V Kronprins Haakon
- eventID: UUID for the sampel
- parentID: UUID for the gear deployment (each MultiNet deployment has a unique parentID)
- eventDate: the date-time when an event occurred, using ISO 8601-1:2019 format (2020-07-27T07:16:03.446Z).
- fieldNumber: human-readable sample ID (e.g. ZOT-001)
- locationID: station name
- decimalLongitude: geographic latitude (in decimal degrees, using the spatial reference system given in geodetic datum)
- decimalLatitude: geographic longitude (in decimal degrees, using the spatial reference system given in geodeticDatum)
- bottomDepthInMeters: bottom depth in meters
- eventRemarks: comments or remarks about the event (free text field)
- gearType: the gear used to take the sample e.g. MultiNet 200 µm
- maximumDepthInMeters: bottom depth of the sampled layer
- minimumDepthInMeters: top depth of the sampled layer
- sampleType: description of the sample type according to a standard list
- fieldSplit: info about whether the sample is splitted. If the sample was split in 2 then fieldSplit = 2
- initialSampleVolume: The volume of water filtered through the plankton net. (initialSampleVolume = (netOpeningArea * (maximumDepthInMeters – minimumDepthInMeters)/field Split), Bongonet opening area: 3.14*(0.3)^2=0.2826 m2
- recordedBy: name of the person who took the samples
- principalInvestigatorName: name of the person in charge of the sample collection
- principalInvestigatorEmail: email address of the person in charge of the sample collection
- principalInvestigatorInstitution: affiliated institution of the person in charge of the sample collection
Header name index - occurrence
- analysedFraction: fraction of the sampled volume that is examined for organism counted
- individualCount: the number of individuals present in the analysed volume (see extra information below)
- phylum, class, order, family, genus & taxonKey-LSID: Taxonomical information for given species according to Worms
- scientificName: full scientific name of the identified organism at the lowest taxonomic level that can be ascertained. The scientificName should be selected from a drop-down menu linked to the list in taxonomy sheet. (e.g Calanus finmarchicus).
- identificationQualifier: A standard term (sp., spp., and indet.) to express the determiner’s doubts about the Identification.
- lifeStage: the age class, life stage, or life form/morph of the organism.
- sizeGroupOperator: describes if the size group is less than or greater than a value (It = less than, gte = greater or equal to)
- sizeGroup: the size group in mm.
- organismRemark: indicates whether it is mesozooplankton, macrozooplankton, rare species
- identificationRemarks: a free text field for adding information relevant to the analysis. Used to indicate the speciemen that were dead. When nothing was remarked they were alive.
- identifiedBy: person who did the lab-analyse
- sampleSizeValue: the sample volume used to calculate the organismQuantity (sampleSizeValue 0 initialSampleVolume *analysedFraction)
- sampleSizeUnit: m3
- organismQuantity: the quantity of the organism per volume water in the environment (organismQuantity = individualCount/sampleSizeValue)
- organismQuantityType: ind/m3
Additional information for some of the fields
individualCount: The number of (all) organisms found in the sample examined
- for “mesozooplankton”, the number of mesozooplankton (medium size zooplankton organisms) encountered in all sub-samples
- for “macrozooplankton”, the number of macrozooplankton (large size zooplankton organisms, total length > 5 mm) encountered, identified in the entire sample
- for “rare” zooplankton, we only enter information about the finding of “rare” zooplankton in the database template, and its absolute number (“organismQuantity”) is not estimated
Funding:
The Nansen Legacy is funded by the Research Council of Norway and the Norwegian Ministry of Education and Research. They provide 50% of the budget while the participating institutions contribute 50% in-kind. The total budget for the Nansen Legacy project is 740 mill. NOK.
The data has been collected during the JC2-1: Nansen Legacy Joint Cruise 2-1 12th July - 29th July 2021 on the research vessel RV Kronprins Haakon (toktnummer 2021708), along a transect from 76N to 82N east of Svalbard. The dataset contains mesozooplankton occurrence. It has been sampled using a MultiNet Midi at 5 distinct depths. Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All specimens are identified to the lowest taxonomical level and the occurrence is given for a specific species and stage or size group as ind/m3.
Quality
Sampling method:
The sampling covers a transect from the central Barents Sea (76N) to the Arctic Ocean (82N) east of Svalbard, including 7 stations (P1 to P7). Each sampling event includes 5 distinct depth layers The depth intervals were from the bottom-200, 200-100, 100-50, 50-20 and 20-0 m. At the deep stations, the sampling depths were from 1000-600, 600-200, 200-50, 50-20 and 20-0 m Zooplankton has been collected using a Multinet Midi (HydroBios, opening: 0.25m2, net length: 250 cm). Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All samples were preserved in 4 % formaldehyde free from acid.
PLEASE NOTE: THIS DATASET CONTAINS TWO COMPLETE DATASETS OF ZOOPLANKTON: ONE FOR SMALL MESOZOOPLANKTON (APPROX BODY SIZE BELOW 2 MM) COLLECTED WITH MULTINET 64 µM AND ONE FOR LARGE MESOZOOPLANKTON (APPROX BODY SIZE ABOVE 2 MM) COLLECTED WITH MULTINET 180 µM MESH SIZE. THE INFO ABOUT WHICH NET IS USED CAN BE FOUND IN gearType in extendedMeasurment andFacts USE EITHER 64 UM OR 180 UM DEPENDING ON WHETHER THE FOCUS IS SMALL OR LARGE MESOZOOPLANKTON
Analyse method:
All samples have been analysed at Institute of Oceanology of the Polish Academy of Sciences (IOPAN). The organisms were identified and counted under a stereomicroscope equipped with an ocular micrometer, according to standard procedures (Harris et al. 2000). Small-sized zooplankters (most of Copepoda, juvenile stages of Pteropoda, Euphausiacea, Ostracoda, Amphipoda and Chaetognatha) were identified and counted in sub-samples obtained from the fixed sample volume by automatic pipette (approximately 500 individuals). Large zooplankters (big Copepoda, Pteropoda, Euphausiacea, Ostracoda, Amphipoda, Decapoda, Appendicularia, Chaetognatha, and Pisces larvae) were sorted out and identified from the whole sample. Representatives of Calanus spp. were identified at the species level based on morphology and prosome lengths of individual copepodid stages (Kwasniewski et al. 2003).
Data structure:
The data is following Darwin Core nomenclature as far as possible but also include variables that aren’t supported by Darwin Core. All information about the sampling such as eventDate, latitude, longitude, depts etc is located in event file while the result such as scientificName, lifeStage, occurrence etc. are found in the occurrence file
Header name index - events
-
expedition: cruise number for R/V Kronprins Haakon
-
eventID: UUID for the sampel
-
parentID: UUID for the gear deployment (each MultiNet deployment has a unique parentID)
-
eventDate: the date-time when an event occurred, using ISO 8601-1:2019 format (2020-07-27T07:16:03.446Z).
-
fieldNumber: human-readable sample ID (e.g. ZOT-001)
-
locationID: station name
-
decimalLongitude: geographic latitude (in decimal degrees, using the spatial reference system given in geodetic datum)
-
decimalLatitude: geographic longitude (in decimal degrees, using the spatial reference system given in geodeticDatum)
-
bottomDepthInMeters: bottom depth in meters
-
eventRemarks: comments or remarks about the event (free text field)
-
gearType: the gear used to take the sample e.g. MultiNet 200 µm
-
maximumDepthInMeters: bottom depth of the sampled layer
-
minimumDepthInMeters: top depth of the sampled layer
-
sampleType: description of the sample type according to a standard list
-
fieldSplit: info about whether the sample is splitted. If the sample was split in 2 then fieldSplit = 2
-
flowmeterStart: only recorded if a flowmeter is used
-
flowmeterStop: only recorded if a flowmeter is used
-
initialSampleVolume: The volume of water filtered through the plankton net. The initial sample volume can be calculated in three ways and should always divided by fieldSplit if the sample is split.
-
theoreticalSampleVolume: Calculated based on sample layer thickness and net opening area (initialSampleVolume = netOpeningArea * (maximumDepthInMeters – minimumDepthInMeters)) Bongonet opening area: 3.14*(0.3)^2=0.2826 m2 WP2 opening area: 3.14*(0.285)^2 = 0.2550 m2 Multinet Midi opening area: 0.25 m2
-
flowmeterSampleVolume: Calculated based on flow-meter readings (initialSampleVolume= (flowmeterStart- flowmeterStop )*( flowmeter pitch = meters/revolution )*netOpeningArea)
-
regressionMultiNetVolume: Calculated based on regression for MultiNet samples (initialSampleVolume = -1.2681+(0.3298*(maximumDepthInMeter – minimumDepthInMeter))
-
initialVolumeMethod: description of which of the three methods were used to calculate the initialSampleSizeValue
-
recordedBy: name of the person who took the samples
-
principalInvestigatorName: name of the person in charge of the sample collection
-
principalInvestigatorEmail: email address of the person in charge of the sample collection
-
principalInvestigatorInstitution: affiliated institution of the person in charge of the sample collection
Header name index - occurrence
- analysedFraction: fraction of the sampled volume that is examined for organism counted
- individualCount: the number of individuals present in the analysed volume (see extra information below)
- scientificName: full scientific name of the identified organism at the lowest taxonomic level that can be ascertained. The scientificName should be selected from a drop-down menu linked to the list in taxonomy sheet. (e.g Calanus finmarchicus).
- identificationQualifier: A standard term (sp., spp., and indet.) to express the determiner’s doubts about the Identification.
- lifeStage: the age class, life stage, or life form/morph of the organism.
- sizeGroupOperator: describes if the size group is less than or greater than a value (It = less than, gte = greater or equal to)
- sizeGroup: the size group in mm.
- organismRemark: indicates whether it is mesozooplankton, macrozooplankton, rare species
- identificationRemarks: a free text field for adding information relevant to the analysis
- identifiedBy: person who did the lab-analyse
- sampleSizeValue: the sample volume used to calculate the organismQuantity (sampleSizeValue 0 initialSampleVolume *analysedFraction)
- sampleSizeUnit: m3
- organismQuantity: the quantity of the organism per volume water in the environment (organismQuantity = individualCount/sampleSizeValue)
- organismQuantityType: ind/m3
Additional information for some of the fields
individualCount: The number of (all) organisms found in the sample examined
- for “mesozooplankton”, the number of mesozooplankton (medium size zooplankton organisms) encountered in all sub-samples
- for “macrozooplankton”, the number of macrozooplankton (large size zooplankton organisms, total length > 5 mm) encountered, identified in the entire sample
- for “rare” zooplankton, we only enter information about the finding of “rare” zooplankton in the database template, and its absolute number (“organismQuantity”) is not estimated
The data has been collected during the JC2-1: Nansen Legacy Joint Cruise 2-1 12th July - 29th July 2021 on the research vessel RV Kronprins Haakon (cruise number 2021708), along a transect from 76N to 82N east of Svalbard. The dataset contains mesozooplankton occurrence. It has been sampled using a BongoNet, HydroBios 60 cm. Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All specimens are identified to the lowest taxonomical level and the occurrence is given for a specific species and stage or size group as ind/m3.
Sampling method:
The sampling covers a transect from the central Barents Sea (76N) to the Arctic Ocean (82N) east of Svalbard, including 7 stations (P1 to P7). Zooplankton has been collected using a BongoNet 60 cm (HydroBios, opening: 0.2827 m2, net length: 250 cm). Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All samples were added 1 ml of Neutral Red Stain stock solution and wait 20 minutes before the samples is rinsed briefly and preserved in 4 % formaldehyde free from acid. The NeutralRed Stain. The samples were analysed within two months after sampling. Neutral Red Stain make it possible to distinguish between dead and alive zooplankton (Elliot and Tang 2009).
PLEASE NOTE: THIS DATASET CONTAINS TWO COMPLETE DATASETS OF ZOOPLANKTON: ONE FOR SMALL MESOZOOPLANKTON (APPROX BODY SIZE BELOW 2 MM) COLLECTED WITH MESH SIZE 64 µM AND ONE FOR LARGE MESOZOOPLANKTON (APPROX BODY SIZE ABOVE 2 MM) COLLECTED WITH MESH SIZE 180 µM MESH SIZE. THE INFO ABOUT WHICH NET IS USED CAN BE FOUND IN gearType. USE EITHER 64 UM OR 180 UM DEPENDING ON WHETHER THE FOCUS IS SMALL OR LARGE MESOZOOPLANKTON
Analyse method:
All samples have been analysed at Institute of Oceanology of the Polish Academy of Sciences (IOPAN). The organisms were identified and counted under a stereomicroscope equipped with an ocular micrometer, according to standard procedures (Harris et al. 2000). Small-sized zooplankters (most of Copepoda, juvenile stages of Pteropoda, Euphausiacea, Ostracoda, Amphipoda and Chaetognatha) were identified and counted in sub-samples obtained from the fixed sample volume by automatic pipette (approximately 500 individuals). Large zooplankters (big Copepoda, Pteropoda, Euphausiacea, Ostracoda, Amphipoda, Decapoda, Appendicularia, Chaetognatha, and Pisces larvae) were sorted out and identified from the whole sample. Representatives of Calanus spp. were identified at the species level based on morphology and prosome lengths of individual copepodid stages (Kwasniewski et al. 2003).
Data structure:
The data is following Darwin Core nomenclature as far as possible but also include variables that aren’t supported by Darwin Core. All information about the sampling such as eventDate, latitude, longitude, depts etc is located in event file while the result such as scientificName, lifeStage, occurrence etc. are found in the occurrence file
Header name index - events
- expedition: cruise number for R/V Kronprins Haakon
- eventID: UUID for the sampel
- parentID: UUID for the gear deployment (each MultiNet deployment has a unique parentID)
- eventDate: the date-time when an event occurred, using ISO 8601-1:2019 format (2020-07-27T07:16:03.446Z).
- fieldNumber: human-readable sample ID (e.g. ZOT-001)
- locationID: station name
- decimalLongitude: geographic latitude (in decimal degrees, using the spatial reference system given in geodetic datum)
- decimalLatitude: geographic longitude (in decimal degrees, using the spatial reference system given in geodeticDatum)
- bottomDepthInMeters: bottom depth in meters
- eventRemarks: comments or remarks about the event (free text field)
- gearType: the gear used to take the sample e.g. MultiNet 200 µm
- maximumDepthInMeters: bottom depth of the sampled layer
- minimumDepthInMeters: top depth of the sampled layer
- sampleType: description of the sample type according to a standard list
- fieldSplit: info about whether the sample is splitted. If the sample was split in 2 then fieldSplit = 2
- initialSampleVolume: The volume of water filtered through the plankton net. (initialSampleVolume = (netOpeningArea * (maximumDepthInMeters – minimumDepthInMeters)/field Split), Bongonet opening area: 3.14*(0.3)^2=0.2826 m2
- recordedBy: name of the person who took the samples
- principalInvestigatorName: name of the person in charge of the sample collection
- principalInvestigatorEmail: email address of the person in charge of the sample collection
- principalInvestigatorInstitution: affiliated institution of the person in charge of the sample collection
Header name index - occurrence
- analysedFraction: fraction of the sampled volume that is examined for organism counted
- individualCount: the number of individuals present in the analysed volume (see extra information below)
- phylum, class, order, family, genus & taxonKey-LSID: Taxonomical information for given species according to Worms
- scientificName: full scientific name of the identified organism at the lowest taxonomic level that can be ascertained. The scientificName should be selected from a drop-down menu linked to the list in taxonomy sheet. (e.g Calanus finmarchicus).
- identificationQualifier: A standard term (sp., spp., and indet.) to express the determiner’s doubts about the Identification.
- lifeStage: the age class, life stage, or life form/morph of the organism.
- sizeGroupOperator: describes if the size group is less than or greater than a value (It = less than, gte = greater or equal to)
- sizeGroup: the size group in mm.
- organismRemark: indicates whether it is mesozooplankton, macrozooplankton, rare species
- identificationRemarks: a free text field for adding information relevant to the analysis. Used to indicate the speciemen that were dead. When nothing was remarked they were alive.
- identifiedBy: person who did the lab-analyse
- sampleSizeValue: the sample volume used to calculate the organismQuantity (sampleSizeValue 0 initialSampleVolume *analysedFraction)
- sampleSizeUnit: m3
- organismQuantity: the quantity of the organism per volume water in the environment (organismQuantity = individualCount/sampleSizeValue)
- organismQuantityType: ind/m3
Additional information for some of the fields
individualCount: The number of (all) organisms found in the sample examined
- for “mesozooplankton”, the number of mesozooplankton (medium size zooplankton organisms) encountered in all sub-samples
- for “macrozooplankton”, the number of macrozooplankton (large size zooplankton organisms, total length > 5 mm) encountered, identified in the entire sample
- for “rare” zooplankton, we only enter information about the finding of “rare” zooplankton in the database template, and its absolute number (“organismQuantity”) is not estimated
Funding:
The Nansen Legacy is funded by the Research Council of Norway and the Norwegian Ministry of Education and Research. They provide 50% of the budget while the participating institutions contribute 50% in-kind. The total budget for the Nansen Legacy project is 740 mill. NOK.
The Nansen Legacy (Arven etter Nansen), The Nansen Legacy
Last metadata update: 2023-02-06T15:15:09Z
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Abstract:
The Nansen Legacy cruise Q1 was part of the seasonal investigation of the northern Barents Sea and adjacent Arctic Basin. The cruise was conducted in 2-24 March 2021 onboard R/V Kronprins Haakon, and focused on studying the physical, chemical and biological conditions along the Nansen Legacy main transect in open waters and within the sea ice. While in sea ice we conducted ten regional scale sea ice helicopter-borne surveys of ice conditions along the Nansen Legacy transect using a helicopter-borne electromagnetic instrument (HEM) EM-bird. This dataset presents processed EM-bird data on total snow and sea-ice thickness along the flight tracks.
This is a contribution to the Research Council of Norway project “Nansen Legacy” (https://arvenetternansen.com/), WP RF-1 “Physical drivers”.
Quality
See the attached docuement “AeN_Q1_202103_HEM_icethickness_metadata_v1.0.pdf” for details on the data acqusition, processing and structure.
The dataset includes water column measurements of spectral beam attenuation and absorption coefficients by non-water constituents. Measurements were collected in May 2021 during cruise 2021704, Q2, in the northern Barents Sea as part of the Nansen Legacy project. The WET Labs ac-s spectrophotometer (Seabird Scientific) were used to collect in situ profiles, with a constant descent velocity (∼0.3 m/s) down to a depth of 350 m, or ~10 m below the ocean floor. Measurements were corrected for temperature and salinity effects. The proportional method was used to correct the scattering error of the absorption measurements, assuming zero absorption at 709 nm. The measurements were binned with 2.0 m (dbar) spacing, applying the median to average the data. See the referenced article for more information.
The data has been collected during the Q2: Nansen Legacy Seasonal Study Q2 from 27 April - 20 May 2021 on research vessel Kronprins Haakon (cruise number 2021704), along a transect in the northern Barents Sea from 76N to 82N. The dataset contains abundance of ice algae marine protists, including ice algae (autotrophic) and protozoa (heterotrophic). Protists were identified and counted with light microscopy using the Utermöhl method and the result are given as cells per liter (cells/L) called organismQuantity.
Quality
Sampling method:
The samples were collected with a slurp gun underneath the ice. The samples were collected by swimming a given distance (the distance is given in the fieldNotes) and sucking up the ice algae attached to the sea ice in this given transect. The mix of ice sluch and ice algae was melted at 4°C. When melted, 95 mL of the sample was transferred into 100 ml brown glass bottle. The samples were preserved using an aldehyde mixture of glutaraldehyde and hexamethylenetetramine-buffered formalin at final concentrations of 0.1% and 1% respectively.
Analysis method:
All samples have been analysed at Institute of Oceanology of the Polish Academy of Sciences (IOPAN). The organisms were identified and counted under an inverted microscope according to the Utermöhl method.
Header name index - events
- expedition: cruise number for R/V Kronprins Haakon
- eventID: UUID for the sample
- parentID: UUID for the gear deployment (each ice core has a unique parentID)
- eventDate: the date-time when an event occurred, using ISO 8601-1:2019 format (2020-07-27T07:16:03.446Z).
- fieldNumber: human-readable sample ID (e.g. IAT-001)
- locationID: station name
- decimalLongitude: geographic latitude (in decimal degrees, using the spatial reference system given in geodetic datum)
- decimalLatitude: geographic longitude (in decimal degrees, using the spatial reference system given in geodeticDatum)
- maximumDepthInCentimeters: bottom depth of the core section in cm
- minimumDepthInCentimeters: upper depth of the core section in cm
- eventRemarks: comments or remarks about the event (free text field)
- gearType: the gear used to take the sample e.g. Ice corer 9 cm
- samplingDepthInMeters: depth sampled
- sampleType: description of the sample type according to a standard list
- recordedBy: name of the person who took the samples
- principalInvestigatorName: name of the person in charge of the sample collection
- principalInvestigatorEmail: email address of the person in charge of the sample collection
- principalInvestigatorInstitution: affiliated institution of the person in charge of the sample collection
Header name index - occurrence
- scientificName: full scientific name of the identified organism at the lowest taxonomic level that can be ascertained. The scientificName should be selected from a drop-down menu linked to the list in taxonomy sheet. (e.g Nitzschia frigida).
- identificationQualifier: A standard term (sp., spp., and indet.) to express the determiner’s doubts about the Identification.
- lifeStage: the life stage (e.g. resting spore) of the organism
- sizeGroupOperator: describes if the size group is less than or greater than a value (It = less than, gte = greater or equal to)
- sizeGroup: the size group in µm.
- organismRemark: indicates e.g. varieties, colony type
- identificationRemarks: a free text field for adding information relevant to the analysis
- identifiedBy: person who did the lab-analyse
- identifiedBy: Drop-down menu linked to list in people-sheet
- dateIdentified: Date for the analysis
- fieldsInCount: Number of fields counted in the microscope
- magnificationMicroscope: The magnification setting used during analysis. Selected from a drop-down menu linked to vocab-sheet
- maxFields: Number of fields in the entire sedimentation chamber (Related to magnification used)
- takenVolumeML: The volume taken for sedimentation in the Utermöhl chamber (the sub-sample taken for analysis)
- totalMeltedVolumeL: The total melted volume in L recorded during sampling.
- addedFSWvolumeL: Volume in L of filtered sea water added to the sample during melting.
- initialVolumeL: The total volume in L of the melted core, measured during sampling. If it wasn’t measured one can use the theoretical calculated core volume based on diameter of the core. initialVolumeL=(totalMeltedVolumeL-addedFSWvolumeL)) or teoreticalCoreVolumeL = coreAreM*(maxDepthCM-minDepthCM)
- sampleSizeValue=((fieldsInCount/maxFields)(takenVolumeML/conversionMLtoL))(dilutionFactorFormaldehyde*dilutionFactorFSW)), dilutionFactorFormaldehyde = 0.95, dilutionFactorFSW=
- sampleSizeUnit: liter (l)
- organismQuantity: the quantity of the organism per volume water in the environment (organismQuantity = individualCount/sampleSizeValue)
- organismQuantityType: cells/l
- cellsPerM2: The quantity (number of cells) of the organism per area (m2). cellsPerM2 = ((individualCount/(sampleSizeValue/initialVolumeL))/coreAreaM
Funding:
The Nansen Legacy is funded by the Research Council of Norway and the Norwegian Ministry of Education and Research. They provide 50% of the budget while the participating institutions contribute 50% in-kind.
We followed line-transect distance sampling survey protocols for estimating abundance of Svalbard reindeer in Sassendalen, Svalbard in July 2021.
Rangifer tarandus
Quality
For the distance sampling survey, we allocated 10 transect lines in north-south direction, from the mountain foothills to the riverbanks, on each side of a large river in Sassendalen, Svalbard. We chose one random latitude for the first line and placed additional parallel transect lines systematically apart 2.5 km east or west from this latitude to reduce the potential of overlapping reindeer observations and violation of the assumption of independence for DS surveys. We chose this systematic orientation across the valley (i.e., riverbed to mountain side or vise-versa) to reduce any bias from potential gradients in animal density related to e.g., plant phenology and/or habitat configuration. The strip length of each of the transects varied depending on the length from the mountain side to the riverbank (1.2 km to 2.9 km). The survey was conducted within the same three-day period 14-17 July 2021.
The 10 transects were walked by one observer at a constant speed (2–3 km h-1) without stops, except during measurements. We used a handheld GPS and a compass to keep the line direction, and single reindeer or clusters were detected on both sides of the transect line with the naked eye. When a reindeer or reindeer group was spotted, the observer looked only in its direction until measurements were taken. To respect the assumption of constant detection along the transect line, no scanning of the surroundings was done when stopping to take measurements. Each observation was measured by laser binoculars (10×42 Leica Geovid) to the nearest meter and a compass was used to measure the angle from the observer to the reindeer. Note that this method only captures the total number of reindeer and no structural information on age and does not record the population structure (i.e., age and sex) of the reindeer. The geographic position of the observer was also recorded. For practical reasons using the laser, measurements were taken to the largest reindeer (e.g., a mother rather than her calf) or the middle individual of a group of adults. From the distance sampling survey, the GPS positions of reindeer groups was calculated and used in the final dataset. For further details and application of the method on Svalbard reindeer see Le Moullec et al. 2017, Le Moullec et al. 2019.
The ice rubble was observed at the beginning of April 2020 near Longyearbyen town, along the shore of Isfjorden, Spitsbergen. There was no such observation in the previous years and after. The rubble appeared after a storm that lasted for several days and left also piles of seaweed onshore 3-4 m above the water level, revealing the wave height. Laser scanning session (in different tidal phase) was performed 9 April 2020 to estimate the size of the rubble and ice block composition. The main ice rubble had size 250x500m with the sail height of ice blocks up to 6 m above water level. Ice floes constructing the rubble were up to 0.9 m thick.
Quality
Data was obtained with Terrestrial Laser Riegl VZ1000, with the next settings: Theta: 30.000..130.000 (0.040) deg Phi: 0.000..360.000 (0.040) deg Program: 950m (150kHz) [2] That gave 9 260 198 Point counts. Sensitive mode was used to obtain points from wet ice surface. Data was processed in RiScan Pro software, filtered with Octree filters and exported to Las 1.2 and ASCII formats with coordinate resolution 0.01 m and 0.1 m to reduce the size.
The data has been collected during the Q2: Nansen Legacy Seasonal Study Q2 27th April - 20th May 2021 on research vessel Kronprins Haakon (cruise number 2021704), along a transect from 76N to 82N east of Svalbard. The dataset contains mesozooplankton occurrence. It has been sampled using a BongoNet, HydroBios 60 cm. Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All specimens are identified to the lowest taxonomical level and the occurrence is given for a specific species and stage or size group as ind/m3.
Sampling method:
The sampling covers a transect from the central Barents Sea (76N) to the Arctic Ocean (82N) east of Svalbard, including 7 stations (P1 to P7). Zooplankton has been collected using a BongoNet 60 cm (HydroBios, opening: 0.2827 m2, net length: 250 cm). Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All samples were added 1 ml of Neutral Red Stain stock solution and wait 20 minutes before the samples is rinsed briefly and preserved in 4 % formaldehyde free from acid. The NeutralRed Stain. The samples were analysed within two months after sampling. Neutral Red Stain make it possible to distinguish between dead and alive zooplankton (Elliot and Tang 2009).
PLEASE NOTE: THIS DATASET CONTAINS TWO COMPLETE DATASETS OF ZOOPLANKTON: ONE FOR SMALL MESOZOOPLANKTON (APPROX BODY SIZE BELOW 2 MM) COLLECTED WITH MESH SIZE 64 µM AND ONE FOR LARGE MESOZOOPLANKTON (APPROX BODY SIZE ABOVE 2 MM) COLLECTED WITH MESH SIZE 180 µM MESH SIZE. THE INFO ABOUT WHICH NET IS USED CAN BE FOUND IN gearType. USE EITHER 64 UM OR 180 UM DEPENDING ON WHETHER THE FOCUS IS SMALL OR LARGE MESOZOOPLANKTON
Analyse method:
All samples have been analysed at Institute of Oceanology of the Polish Academy of Sciences (IOPAN). The organisms were identified and counted under a stereomicroscope equipped with an ocular micrometer, according to standard procedures (Harris et al. 2000). Small-sized zooplankters (most of Copepoda, juvenile stages of Pteropoda, Euphausiacea, Ostracoda, Amphipoda and Chaetognatha) were identified and counted in sub-samples obtained from the fixed sample volume by automatic pipette (approximately 500 individuals). Large zooplankters (big Copepoda, Pteropoda, Euphausiacea, Ostracoda, Amphipoda, Decapoda, Appendicularia, Chaetognatha, and Pisces larvae) were sorted out and identified from the whole sample. Representatives of Calanus spp. were identified at the species level based on morphology and prosome lengths of individual copepodid stages (Kwasniewski et al. 2003).
Data structure:
The data is following Darwin Core nomenclature as far as possible but also include variables that aren’t supported by Darwin Core. All information about the sampling such as eventDate, latitude, longitude, depts etc is located in event file while the result such as scientificName, lifeStage, occurrence etc. are found in the occurrence file
Header name index - events
- expedition: cruise number for R/V Kronprins Haakon
- eventID: UUID for the sampel
- parentID: UUID for the gear deployment (each MultiNet deployment has a unique parentID)
- eventDate: the date-time when an event occurred, using ISO 8601-1:2019 format (2020-07-27T07:16:03.446Z).
- fieldNumber: human-readable sample ID (e.g. ZOT-001)
- locationID: station name
- decimalLongitude: geographic latitude (in decimal degrees, using the spatial reference system given in geodetic datum)
- decimalLatitude: geographic longitude (in decimal degrees, using the spatial reference system given in geodeticDatum)
- bottomDepthInMeters: bottom depth in meters
- eventRemarks: comments or remarks about the event (free text field)
- gearType: the gear used to take the sample e.g. MultiNet 200 µm
- maximumDepthInMeters: bottom depth of the sampled layer
- minimumDepthInMeters: top depth of the sampled layer
- sampleType: description of the sample type according to a standard list
- fieldSplit: info about whether the sample is splitted. If the sample was split in 2 then fieldSplit = 2
- initialSampleVolume: The volume of water filtered through the plankton net. (initialSampleVolume = (netOpeningArea * (maximumDepthInMeters – minimumDepthInMeters)/field Split), Bongonet opening area: 3.14*(0.3)^2=0.2826 m2
- recordedBy: name of the person who took the samples
- principalInvestigatorName: name of the person in charge of the sample collection
- principalInvestigatorEmail: email address of the person in charge of the sample collection
- principalInvestigatorInstitution: affiliated institution of the person in charge of the sample collection
Header name index - occurrence
- analysedFraction: fraction of the sampled volume that is examined for organism counted
- individualCount: the number of individuals present in the analysed volume (see extra information below)
- phylum, class, order, family, genus & taxonKey-LSID: Taxonomical information for given species according to Worms
- scientificName: full scientific name of the identified organism at the lowest taxonomic level that can be ascertained. The scientificName should be selected from a drop-down menu linked to the list in taxonomy sheet. (e.g Calanus finmarchicus).
- identificationQualifier: A standard term (sp., spp., and indet.) to express the determiner’s doubts about the Identification.
- lifeStage: the age class, life stage, or life form/morph of the organism.
- sizeGroupOperator: describes if the size group is less than or greater than a value (It = less than, gte = greater or equal to)
- sizeGroup: the size group in mm.
- organismRemark: indicates whether it is mesozooplankton, macrozooplankton, rare species
- identificationRemarks: a free text field for adding information relevant to the analysis. Used to indicate the speciemen that were dead. When nothing was remarked they were alive.
- identifiedBy: person who did the lab-analyse
- sampleSizeValue: the sample volume used to calculate the organismQuantity (sampleSizeValue 0 initialSampleVolume *analysedFraction)
- sampleSizeUnit: m3
- organismQuantity: the quantity of the organism per volume water in the environment (organismQuantity = individualCount/sampleSizeValue)
- organismQuantityType: ind/m3
Additional information for some of the fields
individualCount: The number of (all) organisms found in the sample examined
- for “mesozooplankton”, the number of mesozooplankton (medium size zooplankton organisms) encountered in all sub-samples
- for “macrozooplankton”, the number of macrozooplankton (large size zooplankton organisms, total length > 5 mm) encountered, identified in the entire sample
- for “rare” zooplankton, we only enter information about the finding of “rare” zooplankton in the database template, and its absolute number (“organismQuantity”) is not estimated
Funding:
The Nansen Legacy is funded by the Research Council of Norway and the Norwegian Ministry of Education and Research. They provide 50% of the budget while the participating institutions contribute 50% in-kind. The total budget for the Nansen Legacy project is 740 mill. NOK.