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Metadata Report for BODC Series Reference Number 2138694


Metadata Summary

Data Description

Data Category Water sample data
Instrument Type
NameCategories
Non-toxic sea water supply  continuous water samplers
SEAL Analytical QuAAtro Autoanalyser  autoanalysers; spectrophotometers
Instrument Mounting research vessel
Originating Country United Kingdom
Originator Mr Mark Stinchcombe
Originating Organization National Oceanography Centre, Southampton
Processing Status banked
Online delivery of data Download available - Ocean Data View (ODV) format
Project(s) OSMOSIS
 

Data Identifiers

Originator's Identifier JC090_GPUMP_NUTS_257:
BODC Series Reference 2138694
 

Time Co-ordinates(UT)

Start Time (yyyy-mm-dd hh:mm) 2013-09-02 11:15
End Time (yyyy-mm-dd hh:mm) 2013-09-13 17:39
Nominal Cycle Interval -
 

Spatial Co-ordinates

Southernmost Latitude 48.35987 N ( 48° 21.6' N )
Northernmost Latitude 49.00087 N ( 49° 0.1' N )
Westernmost Longitude 16.28092 W ( 16° 16.9' W )
Easternmost Longitude 15.86724 W ( 15° 52.0' W )
Positional Uncertainty 0.05 to 0.1 n.miles
Minimum Sensor or Sampling Depth 5.0 m
Maximum Sensor or Sampling Depth 5.0 m
Minimum Sensor or Sampling Height -
Maximum Sensor or Sampling Height -
Sea Floor Depth -
Sea Floor Depth Source -
Sensor or Sampling Distribution Unspecified -
Sensor or Sampling Depth Datum Unspecified -
Sea Floor Depth Datum Unspecified -
 

Parameters

BODC CODERankUnitsTitle
AADYAA011DaysDate (time from 00:00 01/01/1760 to 00:00 UT on day)
AAFDZZ011DaysTime (time between 00:00 UT and timestamp)
ALATGP011DegreesLatitude north relative to WGS84 by unspecified GPS system
ALONGP011DegreesLongitude east relative to WGS84 by unspecified GPS system
NTRIAAZX1Micromoles per litreConcentration of nitrite {NO2- CAS 14797-65-0} per unit volume of the water body [unknown phase] by colorimetric autoanalysis
NTRZAATX1Micromoles per litreConcentration of nitrate+nitrite {NO3+NO2} per unit volume of the water body [dissolved plus reactive particulate phase] by colorimetric autoanalysis
PHOSAATX1Micromoles per litreConcentration of phosphate {PO43- CAS 14265-44-2} per unit volume of the water body [dissolved plus reactive particulate phase] by colorimetric autoanalysis
SLCAAATX1Micromoles per litreConcentration of silicate {SiO44- CAS 17181-37-2} per unit volume of the water body [dissolved plus reactive particulate phase] by colorimetric autoanalysis

Definition of Rank

  • Rank 1 is a one-dimensional parameter
  • Rank 2 is a two-dimensional parameter
  • Rank 0 is a one-dimensional parameter describing the second dimension of a two-dimensional parameter (e.g. bin depths for moored ADCP data)

Problem Reports

No Problem Report Found in the Database


Data Access Policy

Open Data supplied by Natural Environment Research Council (NERC)

You must always use the following attribution statement to acknowledge the source of the information: "Contains data supplied by Natural Environment Research Council."


Narrative Documents

SEAL Analytical QuAAtro colorimetric autoanalyser

The SEAL QuAAtro high Performance Microflow Analyzer is the latest generation of the original world-class TechniconTM Segmented Flow Analysis (SFA) systems.

A basic SFA system consists of an autosampler, a peristaltic pump, a chemistry manifold, a detector and data acquisition software. Sample and reagents are pumped continuously through the chemistry manifold. Air bubbles are introduced at regular intervals forming unique reaction segments which are mixed using glass coils. Glass is ideal, as it is inert, stays clean and enables easy visual checks.

In SFA, reactions run to completion and the ratio of sample to reagents in the detector reaches a constant maximum value. This results in ultra-low detection limits and exceptional reproducibility. Variations in reaction time, temperature and sample matrix do not affect the results as they do in other colorimetric techniques, such as flow injection analysis, where the reaction is not brought to completion.

QuAAtro is a microflow SFA system, the internal diameter of all glassware being 1 mm. This reduces reagent consumption and increases throughput, with most methods running at 100 - 120 samples hour. The integrated enclosed manifold and detector are heated to 37 °C. Flow stability is ensured as the optimal bubble frequency for each method is programmed by silent air valves. Automatic start-up, method changeover and shutdown allows true unattended operation and overnight running. QuAAtro checks its own performance, with automatic monitoring of noise, drift, bubble pattern and light energy, before and during a run.

Up to four methods can run at the same time on one console, and there is a special 5-channel version for nutrients in seawater. Two consoles can be combined to give an 8-channel system.

Further details can be found in the manufacturer's specification sheet.

Non-toxic (underway) sea water supply

A source of uncontaminated near-surface (commonly 3 to 7 m) seawater pumped continuously to shipboard laboratories on research vessels. There is typically a temperature sensor near the intake (known as the hull temperature) to provide measurements that are as close as possible to the ambient water temperature. The flow from the supply is typically directed through continuously logged sensors such as a thermosalinograph and a fluorometer. Water samples are often collected from the non-toxic supply. The system is also referred to as the underway supply.

JC090 inorganic nutrients sampling document

Originator's protocol for data acquisition

The following contains extracts from the JC090 cruise report.

The RRS James Cook 090 cruise was the concluding phase of the fieldwork for the Ocean Surface Mixing, Ocean Sub-mesoscale Interaction Study (OSMOSIS) consortium and sought to recover 9 moorings and 2 gliders to conduct hydrographic and biogeochemical measurements for mooring and glider calibration, and to obtain opportunistic measurements of upper-ocean microstructure and air-sea CO2 fluxes. The cruise departed on the 30 August 2013 from the port of Vigo, Spain and returned on the 17 September 2013 at the port of Santander, Spain.

Sample collection

A CTD rosette was used for collecting water samples from various depths between the surface and 200 m. The rosette had 24 Niskin bottles with a 20 litre capacity. Samples were also collected from the ships underway system (~ 5 m depth) approximately every 6 hours starting at 11:00 hours (GMT) on 02 Sep 2013 and finishing at 17:00 hours (GMT) on 13 Sep 2013.

A 10 ml water sample collected for nutrient analysis was placed in a 15 ml labeled centrifuge tube. The sample was then frozen for later analysis at the National Oceanography Centre, Southampton.

Sample analysis

The nutrients were analysed at NOCS using the SEAL Analytical UK Ltd segmented-flow autoanalyser (QuAAtro), for nitrate, nitrite, phosphate and silicate, using the methodology of Kirkwood (1996). The following calibrations were applied:

  • Nitrate and Nitrite linear fit, r2 = 1.000 (calibration concentrations - 3.034, 6.067, 9.101,12.134 µmol l-1)
  • Silicate linear fit, r2 = 0.9999 (calibration concentrations - 2.482, 4.964, 7.445, 9.927 µmol l-1)
  • Nitrite linear fit, r2 = 0.9999 (calibration concentrations - 0.507, 1.014, 1.521, 2.027 µmol l-1)
  • Phosphate linear fit, r2 = 0.9999 (calibration concentrations - 0.502, 1.005, 1.507, 2.010 µmol l-1)

BODC data processing procedures

Inorganic nutrients data were supplied to BODC in Microsoft Excel format and values were extracted for loading into BODC's ocean database under the ORACLE Relational Database Management System. Data that were considered unrealistic were flagged suspect.

Content of data series

Originator's Parameter Unit Description BODC Parameter code BODC Unit Comments
Nitrate and Nitrite (CTD and underway samples) µmol l-1 Concentration of nitrate+nitrite {NO3+NO2} per unit volume of the water body [unknown phase] by colorimetric autoanalysis NTRZAATX µmol l-1 N/A
Silicate (CTD and underway samples) µmol l-1 Concentration of silicate {SiO4} per unit volume of the water body [unknown phase] by colorimetric autoanalysis SLCAAATX µmol l-1 N/A
Nitrite (CTD and underway samples) µmol l-1 Concentration of nitrite {NO2} per unit volume of the water body [unknown phase] by colorimetric autoanalysis NTRIAAZX µmol l-1 N/A
Phosphate (CTD and underway samples) µmol l-1 Concentration of phosphate {PO4} per unit volume of the water body [unknown phase] by colorimetric autoanalysis PHOSAATX µmol l-1 N/A

Data quality report

Negative nitrite values are below the detection limit of the analyser for the CTD and underway samples. Negative silicate values were also present due to the same reason for the CTD samples. These values have been assigned an 'M' flag by BODC.

References

Kirkwood, D. S. (1996.) Nutrients: Practical notes on their determination in seawater. In: ICES Techniques in Marine Environmental Sciences Report 17, International Council for the Exploration of the Seas, Copenhagen (1996), p.25

Naveira-Garabato A. et al. (2013). 'Ocean Surface Mixing, Ocean Sub-mesoscale Interaction Study (OSMOSIS)'. Cruise Report No. 25 National Oceanography Centre, Southampton.


Project Information

Ocean Surface Mixing, Ocean Sub-mesoscale Interaction Study (OSMOSIS)

Background

The Ocean Surface Mixing, Ocean Sub-mesoscale Interaction Study (OSMOSIS) consortium was funded to deliver NERC's Ocean Surface Boundary Layer (OSBL) programme. Commencing in 2011, this multiple year study will combine traditional observational techniques, such as moorings and CTDs, with the latest autonomous sampling technologies (including ocean gliders), capable of delivering near real-time scientific measurements through the water column.

The OSMOSIS consortium aims to improve understanding of the OSBL, the interface between the atmosphere and the deeper ocean. This layer of the water column is thought to play a pivotal role in global climate and the productivity of our oceans.

OSMOSIS involves collaborations between scientists at various universities (Reading, Oxford, Bangor, Southampton and East Anglia) together with researchers at the National Oceanography Centre (NOC), Scottish Association for Marine Science (SAMS) and Plymouth Marine Laboratory (PML). In addition, there are a number of project partners linked to the consortium.

Scientific Objectives

  • The primary goal of the fieldwork component of OSMOSIS is to obtain a year-long time series of the properties of the OSBL and its controlling 3D physical processes. This is achieved with an array of moorings (two nested clusters of 4 moorings, each centred around a central mooring) and gliders deployed near the Porcupine Abyssal Plain (PAP) observatory. Data obtained from this campaign will help with the understanding of these processes and subsequent development of associated parameterisations.
  • OSMOSIS will attempt to create parameterisations for the processes which determine the evolving stratification and potential vorticity budgets of the OSBL.
  • The overall legacy of OSMOSIS will be to develop new (physically based and observationally supported) parameterisations of processes that deepen and shoal the OSBL, and to implement and evaluate these parameterisations in a state-of-the-art global coupled climate model, facilitating improved weather and climate predictions.

Fieldwork

Three cruises are directly associated with the OSMOSIS consortium. Preliminary exploratory work in the Clyde Sea (September 2011) to hone techniques and strategies, followed by a mooring deployment and recovery cruise in the vicinity of the Porcupine Abyssal Plain (PAP) observatory (in late Summer 2012 and 2013 respectively). Additional opportunist ship time being factored in to support the ambitious glider operations associated with OSMOSIS.

Instrumentation

Types of instrumentation and measurements associated with the OSMOSIS observational campaign:

  • Ocean gliders
  • Wave rider buoys
  • Towed SeaSoar surveys
  • Microshear measurements
  • Moored current meters, conductivity-temperature sensors and ADCPs
  • Traditional shipboard measurements (including CTD, underway, discrete nutrients, LADCP, ADCP).

Contacts

Collaborator Organisation
Prof. Stephen Belcher University of Reading, U.K
Dr. Alberto C Naveira Garabato University of Southampton, U.K

Data Activity or Cruise Information

Cruise

Cruise Name JC090
Departure Date 2013-08-31
Arrival Date 2013-09-16
Principal Scientist(s)Alberto C Naveira Garabato (University of Southampton School of Ocean and Earth Science)
Ship RRS James Cook

Complete Cruise Metadata Report is available here


Fixed Station Information


No Fixed Station Information held for the Series


BODC Quality Control Flags

The following single character qualifying flags may be associated with one or more individual parameters with a data cycle:

Flag Description
Blank Unqualified
< Below detection limit
> In excess of quoted value
A Taxonomic flag for affinis (aff.)
B Beginning of CTD Down/Up Cast
C Taxonomic flag for confer (cf.)
D Thermometric depth
E End of CTD Down/Up Cast
G Non-taxonomic biological characteristic uncertainty
H Extrapolated value
I Taxonomic flag for single species (sp.)
K Improbable value - unknown quality control source
L Improbable value - originator's quality control
M Improbable value - BODC quality control
N Null value
O Improbable value - user quality control
P Trace/calm
Q Indeterminate
R Replacement value
S Estimated value
T Interpolated value
U Uncalibrated
W Control value
X Excessive difference

SeaDataNet Quality Control Flags

The following single character qualifying flags may be associated with one or more individual parameters with a data cycle:

Flag Description
0 no quality control
1 good value
2 probably good value
3 probably bad value
4 bad value
5 changed value
6 value below detection
7 value in excess
8 interpolated value
9 missing value
A value phenomenon uncertain
B nominal value
Q value below limit of quantification