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Metadata Report for BODC Series Reference Number 2094578


Metadata Summary

Data Description

Data Category Water sample data
Instrument Type
NameCategories
Lever Action Niskin Bottle  discrete water samplers
Varian 3300 Gas Chromatograph  gas chromatographs
Instrument Mounting lowered unmanned submersible
Originating Country Belgium
Originator Prof Lei Lei
Originating Organization Free University of Brussels, Laboratory of Chemical Oceanography and Water Geochemistry
Processing Status banked
Online delivery of data Download available - Ocean Data View (ODV) format
Project(s) OMEX I
 

Data Identifiers

Originator's Identifier DI216_CTD_TMXX_14:CTD21
BODC Series Reference 2094578
 

Time Co-ordinates(UT)

Start Time (yyyy-mm-dd hh:mm) 1995-09-02 05:24
End Time (yyyy-mm-dd hh:mm) -
Nominal Cycle Interval -
 

Spatial Co-ordinates

Latitude 48.58160 N ( 48° 34.9' N )
Longitude 13.32146 W ( 13° 19.3' W )
Positional Uncertainty 0.05 to 0.1 n.miles
Minimum Sensor or Sampling Depth 31.1 m
Maximum Sensor or Sampling Depth 149.8 m
Minimum Sensor or Sampling Height 4198.3 m
Maximum Sensor or Sampling Height 4317.0 m
Sea Floor Depth 4348.1 m
Sea Floor Depth Source PEVENT
Sensor or Sampling Distribution Unspecified -
Sensor or Sampling Depth Datum Unspecified -
Sea Floor Depth Datum Unspecified -
 

Parameters

BODC CODERankUnitsTitle
ADEPZZ011MetresDepth (spatial coordinate) relative to water surface in the water body
ALXXLGD21Nanomoles per litreConcentration of aluminium {Al CAS 7429-90-5} per unit volume of the water body [dissolved plus reactive particulate <0.4/0.45um phase] by filtration and lumogallion fluorescence
BOTTFLAG1Not applicableSampling process quality flag (BODC C22)
SAMPRFNM1DimensionlessSample reference number

Definition of BOTTFLAG

BOTTFLAGDefinition
0The sampling event occurred without any incident being reported to BODC.
1The filter in an in-situ sampling pump physically ruptured during sample resulting in an unquantifiable loss of sampled material.
2Analytical evidence (e.g. surface water salinity measured on a sample collected at depth) indicates that the water sample has been contaminated by water from depths other than the depths of sampling.
3The feedback indicator on the deck unit reported that the bottle closure command had failed. General Oceanics deck units used on NERC vessels in the 80s and 90s were renowned for reporting misfires when the bottle had been closed. This flag is also suitable for when a trigger command is mistakenly sent to a bottle that has previously been fired.
4During the sampling deployment the bottle was fired in an order other than incrementing rosette position. Indicative of the potential for errors in the assignment of bottle firing depth, especially with General Oceanics rosettes.
5Water was reported to be escaping from the bottle as the rosette was being recovered.
6The bottle seals were observed to be incorrectly seated and the bottle was only part full of water on recovery.
7Either the bottle was found to contain no sample on recovery or there was no bottle fitted to the rosette position fired (but SBE35 record may exist).
8There is reason to doubt the accuracy of the sampling depth associated with the sample.
9The bottle air vent had not been closed prior to deployment giving rise to a risk of sample contamination through leakage.

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

Public domain data

These data have no specific confidentiality restrictions for users. However, users must acknowledge data sources as it is not ethical to publish data without proper attribution. Any publication or other output resulting from usage of the data should include an acknowledgment.

The recommended acknowledgment is

"This study uses data from the data source/organisation/programme, provided by the British Oceanographic Data Centre and funded by the funding body."


Narrative Documents

Varian 3300 Gas Chromatograph

The Varian 3300 gas chromatograph separates and analyses gas mixtures in water or air. The instrument includes an injector, autosampler, capillary column and one or more detectors. The sample is vapourised then transported along the column within an inert gas flow.

The column oven accepts packed or fused silica capillary columns, while the instrument accommodates a range of standard and capillary injectors and a variety of detectors. The carrier gas may be air, helium, hydrogen, nitrogen or argon-methane, depending on the type of detector used. Optional carrier gas and oxygen filters may also be incorporated into the instrument. The equipment is controlled by a built-in microcomputer and can perform electron-impact, chemical ionisation, and negative ion analysis. The instrument was originally manufactured by Varian, Inc., which was bought by Agilent Technologies in 2010.

Specifications

Detector type FID TSD ECD FPD TCD ELCD PID
Linear Dynamic range 107

105 (N)

104 (P)

104 (N2 carrier gas)

105 (P)

103 (S)

106 (butane)

> 106 (halogens)

105 (N)

104 (S)

104
Detectivity > 2 pg C sec-1

> 0.2 pg N sec-1 (azobenzene)

> 0.1 pg P sec-1 (malathion)

0.05 pg (Lindane)

1 pg P sec-1 (in Tributylphosphate)

0.1 ng S sec-1 (in n-hexane thiol)

3x10-10 g mL-1 (butane)

2.5 pg (Halogens, heptachlor)

10 pg (N, azobenzene)

10 pg (S, ethion)

10 pg (benzene)
Noise

50 msec: < 4x10-14 A

270 msec: < 1x10-14 A

50 msec: < 2x10-14 A

270 msec: < 1x10-14 A

 

50 msec: < 10x10-12 A

1 sec: < 2x10-12 A

< 1.0 µV < 2x10-13 A < 1.0x10-13 A
Sensitivity 15 mCoul g-1 C (N2 carrier gas)            
Specificity  

P/N 2:1

N/C 5x104:1

P/C 105:1

 

P/C 105:1

S/C >103

 

CI/CH >106

N/HC > 107

S/HC 105

 
Temperature Range (°C) 120 to 420 120 to 420 120 to 420 120 to 350 120 to 300 120 to 350 120 to 280

FID- Flame Ionization
TSD- Thermionic Sensitive
ECD- Electron capture
FPD- Flame photometric
TCD- Thermal Conductivity
ELCD- Electrolytic Conductivity
PID- Photo-ionization

Further details can be found in the manufacturer's manual.

Niskin Bottle

The Niskin bottle is a device used by oceanographers to collect subsurface seawater samples. It is a plastic bottle with caps and rubber seals at each end and is deployed with the caps held open, allowing free-flushing of the bottle as it moves through the water column.

Standard Niskin

The standard version of the bottle includes a plastic-coated metal spring or elastic cord running through the interior of the bottle that joins the two caps, and the caps are held open against the spring by plastic lanyards. When the bottle reaches the desired depth the lanyards are released by a pressure-actuated switch, command signal or messenger weight and the caps are forced shut and sealed, trapping the seawater sample.

Lever Action Niskin

The Lever Action Niskin Bottle differs from the standard version, in that the caps are held open during deployment by externally mounted stainless steel springs rather than an internal spring or cord. Lever Action Niskins are recommended for applications where a completely clear sample chamber is critical or for use in deep cold water.

Clean Sampling

A modified version of the standard Niskin bottle has been developed for clean sampling. This is teflon-coated and uses a latex cord to close the caps rather than a metal spring. The clean version of the Levered Action Niskin bottle is also teflon-coated and uses epoxy covered springs in place of the stainless steel springs. These bottles are specifically designed to minimise metal contamination when sampling trace metals.

Deployment

Bottles may be deployed singly clamped to a wire or in groups of up to 48 on a rosette. Standard bottles and Lever Action bottles have a capacity between 1.7 and 30 L. Reversing thermometers may be attached to a spring-loaded disk that rotates through 180° on bottle closure.

Particulate Trace Metals for cruises on Belgica, Charles Darwin and RRS Discovery

Document History

Converted from CDROM documentation.

Content of data series

ALCNAAP2 Particulate aluminium content
Atomic absorption (0.45/0.4 µm pore filtered)
Per Cent
ALCNAAPC Particulate aluminium content
Atomic absorption (centrifuged)
Per Cent
CACNICP2 Particulate calcium content
ICP after acid digestion (0.45/0.4 µm pore filtered)
Per Cent
CACNICPC Particulate calcium content
ICP after acid digestion (centrifuged)
Per Cent
CDCNAAP2 Particulate cadmium content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
CDCNAAPC Particulate cadmium content
Atomic absorption (centrifuged)
Parts per million
COCNAAP2 Particulate cobalt content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
COCNAAPC Particulate cobalt content
Atomic absorption (centrifuged)
Parts per million
CRCNAAP2 Particulate chromium content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
CRCNAAPC Particulate chromium content
Atomic absorption (centrifuged)
Parts per million
CUCNAAP2 Particulate copper content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
CUCNAAPC Particulate copper content
Atomic absorption (centrifuged)
Parts per million
FECNAAP2 Particulate total iron content
Atomic absorption (0.45/0.4 µm pore filtered)
Per Cent
FECNAAPC Particulate total iron content
Atomic absorption (centrifuged)
Per Cent
KXCNICP2 Particulate potassium content
ICP after acid digestion (0.45/0.4 µm pore filtered)
Per Cent
KXCNICPC Particulate potassium content
ICP after acid digestion (centrifuged)
Per Cent
LICNAAP2 Particulate lithium content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
MGCNICP2 Particulate magnesium content
ICP after acid digestion (0.45/0.4 µm pore filtered)
Per Cent
MGCNICPC Particulate magnesium content
ICP after acid digestion (centrifuged)
Per Cent
MNCNAAP2 Particulate total manganese content
Atomic absorption (0.45/0.4 µm pore filtered)
Per Cent
MNCNAAPC Particulate total manganese content
Atomic absorption (centrifuged)
Per Cent
NACNICP2 Particulate sodium content
ICP after acid digestion (0.45/0.4 µm pore filtered)
Per Cent
NACNICPC Particulate sodium content
ICP after acid digestion (centrifuged)
Per Cent
NICNAAP2 Particulate nickel content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
NICNAAPC Particulate nickel content
Atomic absorption (centrifuged)
Parts per million
PBCNAAP2 Particulate lead content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
PBCNAAPC Particulate lead content
Atomic absorption (centrifuged)
Parts per million
SICNICP2 Particulate silicon content
ICP after acid digestion (0.45/0.4 µm pore filtered)
Per Cent
SICNICPC Particulate silicon content
ICP after acid digestion (centrifuged)
Per Cent
ZNCNAAP2 Particulate zinc content
Atomic absorption (0.45/0.4 µm pore filtered)
Parts per million
ZNCNAAPC Particulate zinc content
Atomic absorption (centrifuged)
Parts per million

Data Originator

Dr Lei Chou, ULB, Brussels, Belgium.

Sampling strategy and methodology

CruisesBelgica BG9309, BG9322, BG9412 and BG9506, Charles Darwin CD84 and CD94 and RRS Discovery DI216

Samples were obtained using one of two protocols. The protocol used may be identified by the gear code in the EVENT entry for the data (SAP or GPCENT).

SAP collection

Challenger Oceanics in-situ stand-alone pumps (SAPs) were used to sample particulate material. The instruments were deployed on kevlar rope from an auxiliary winch and were switched on and off by a programmable timer to ensure that the pump only sampled when in position at the desired depth. Membrane filters with a 0.4 micron pore size were used to collect the particulate material.

On recovery the filters were rinsed and dried in clean conditions. Back at the home laboratory, the suspended particulate material was ultrasonically detached from the filter for analysis.

GPCENT collection.

Suspended particulate matter was collected by continuous flow centrifugation using an Alpha-Laval oil purifier (model MAB 104) specially coated for oceanographic use. Water supply was adjusted to approximately 1 cubic metre per hour. Samples were collected both when the ship was on station and steaming between stations for about 6-10 hours.

Samples were taken from the centrifuge body using a stainless steel spatula, stored in acid-washed PET vials and immediately deep frozen. After weighing (wet weight) the sample was subdivided for C/N, trace metal and isotope analysis.

The samples were analysed for Al, Cu, Fe, Mn, Cr, Ni, Co, Zn, Cd and Pb by direct injection of solid samples as slurries using electrothermal atomic absorption spectroscopy in a Varian Spectraa-300 spectrometer with Zeeman correction.

The analytical conditions were as follows:

Al Wavelength 394.4nm
Slit width 0.5nm
Atomisation support Platform
Drying 110 °C to 300 °C in 60 seconds
Ashing 1000 °C, 10 second ramp, 20 second hold
Atomisation 2600 °C, maximum power, 4 second hold, no gas stop
Modifier Pd, Si, Ca, K, Mg, Fe, Na, P
Cd Wavelength 228.8nm
Slit width 0,5nm
Atomisation support Platform
Drying 110 °C to 280 °C in 70 seconds
Ashing 600 °C, 5 second ramp, 20 second hold
Atomisation 2300 °C, maximum power, 2 second hold, gas stop
Modifier Mg/PO4
Co Wavelength 240.7nm
Slit width 0.2nm
Atomisation support Tube
Drying 50 °C to 160 °C in 70 seconds
Ashing 300 °C, 5 second ramp, 5 second hold, cool to 100 °C
Atomisation 2600 °C, maximum power, 2 second hold, gas stop
Modifier None
Cr Wavelength 357.9nm
Slit width 0.2nm
Atomisation support Tube
Drying 50 °C to 165 °C in 60 seconds
Ashing 1050 °C, 5 second ramp, 20 second hold, cool to 100 °C
Atomisation 2650 °C, maximum power, 3 second hold, gas stop
Modifier None
Cu Wavelength 324.7nm
Slit width 0.5nm
Atomisation support Tube
Drying 50 °C to 150 °C in 70 seconds
Ashing 950 °C, 5 second ramp, 30 second hold
Atomisation 2500 °C, maximum power, 2 second hold, gas stop
Modifier Pd/Mg
Fe Wavelength 302.1nm
Slit width 0.2nm
Atomisation support Tube
Drying 50 to 130 °C in 50 seconds
Ashing 200 °C, 5 second ramp, 20 second hold
Atomisation 2400 °C, maximum power, 2 second hold, no gas stop
Modifier None
Mn Wavelength 403.1nm
Slit width 0.2nm
Atomisation support Platform
Drying 110 °C to 400 °C in 80 seconds
Ashing 1500 °C, 5 second ramp, 20 second hold, cool to 100 °C
Atomisation 2700 °C, maximum power, 3 second hold, gas stop
Modifier Pt
Ni Wavelength 232.0nm
Slit width 0.2nm
Atomisation support Tube
Drying 50 °C to 150 °C in 70 seconds
Ashing 1100 °C, 5 second ramp, 20 second hold, cool to 100 °C
Atomisation 2600 °C, maximum power, 3 second hold, gas stop
Modifier Pd/Mg
Pb Wavelength 217.0nm
Slit width 1.0nm
Atomisation support Platform
Drying 110 °C to 370 °C in 70 seconds
Ashing 800 °C, 5 second ramp, 20 second hold
Atomisation 2600 °C, maximum power, 3 second hold, gas stop
Modifier Pd/Mg
Zn Wavelength 213.9nm
Slit width 1.0nm
Atomisation support Platform
Drying 110 °C to 300 °C in 60 seconds
Ashing 950 °C, 5 second ramp, 20 second hold
Atomisation 2600 °C, maximum power, 2 second hold, gas stop
Modifier Mg

Peak area measurement mode was used for all the above elements.

Major elements were determined by Inductively Coupled Plasma emission spectroscopy after complete digestion of the samples by an HNO3/HCl/HF mixture in a Teflon bomb in a microwave oven.

If there was insufficient material for the direct injection technique, trace elements were also determined on the digested samples either by ICP, if present in sufficient concentration, or by AA. The parameter codes have been set up to indicate the predominant method for the element.

Comments on data quality

It is reported in the OMEX I final report that ULB participated in the QUASIMEME intercalibration exercise and obtained the following results. The certified values are given in brackets.

North Sea Baltic
Al (%) 3.46 (3.5) 6.1 (6.4)
Cd (ppb) 1.487 (1.425) 0.120 (0.123)
Cu (ppb) 26.02 (24) 20.8 (19.1)
Pb (ppb) 44.6 (45) 45.7 (44.9)
Zn (ppb) 172 (170) 112 (123)

The good agreement with the certified values gives confidence in the ULB particulate trace metal data.

Charles Darwin cruise CD94

A number of the filters were reported by the data originator to have anomalously high concentrations for some metals that have been attributed to sample contamination. These have been flagged as 'L' in the database.

RRS Discovery cruise DI216

The CTD cable used on this cruise was in very poor condition and a clearly visible plume of rust could be seen in the water each time the CTD was deployed. Although the SAPs were deployed on kevlar rope, the SAP sampling had to be preceded by a CTD cast to determine the water column structure for assigning the sampling depths.

There is clear evidence in the iron data that most of the SAP samples were polluted by the plume generated by this cast. Consequently, the metal data have been heavily flagged 'L' to reflect the comments of the data originator.

In view of this obvious contamination problem any of the SAP data from this cruise, whatever its associated flag value, should be used with caution.


Project Information

Ocean Margin EXchange (OMEX) I

Introduction

OMEX was a European multidisciplinary oceanographic research project that studied and quantified the exchange processes of carbon and associated elements between the continental shelf of western Europe and the open Atlantic Ocean. The project ran in two phases known as OMEX I (1993-1996) and OMEX II - II (1997-2000), with a bridging phase OMEX II - I (1996-1997). The project was supported by the European Union under the second and third phases of its MArine Science and Technology Programme (MAST) through contracts MAS2-CT93-0069 and MAS3-CT97-0076. It was led by Professor Roland Wollast from Université Libre de Bruxelles, Belgium and involved more than 100 scientists from 10 European countries.

Scientific Objectives

The aim of the Ocean Margin EXchange (OMEX) project was to gain a better understanding of the physical, chemical and biological processes occurring at the ocean margins in order to quantify fluxes of energy and matter (carbon, nutrients and other trace elements) across this boundary. The research culminated in the development of quantitative budgets for the areas studied using an approach based on both field measurements and modeling.

OMEX I (1993-1996)

The first phase of OMEX was divided into sub-projects by discipline:

  • Physics
  • Biogeochemical Cycles
  • Biological Processes
  • Benthic Processes
  • Carbon Cycling and Biogases

This emphasises the multidisciplinary nature of the research.

The project fieldwork focussed on the region of the European Margin adjacent to the Goban Spur (off the coast of Brittany) and the shelf break off Tromsø, Norway. However, there was also data collected off the Iberian Margin and to the west of Ireland. In all a total of 57 research cruises (excluding 295 Continuous Plankton Recorder tows) were involved in the collection of OMEX I data.

Data Availability

Field data collected during OMEX I have been published by BODC as a CD-ROM product, entitled:

  • OMEX I Project Data Set (two discs)

Further descriptions of this product and order forms may be found on the BODC web site.

The data are also held in BODC's databases and subsets may be obtained by request from BODC.


Data Activity or Cruise Information

Data Activity

Start Date (yyyy-mm-dd) 1995-09-02
End Date (yyyy-mm-dd) 1995-09-02
Organization Undertaking ActivityUniversity of Southampton Department of Oceanography (now University of Southampton School of Ocean and Earth Science)
Country of OrganizationUnited Kingdom
Originator's Data Activity IdentifierDI216_CTD_CTD21
Platform Categorylowered unmanned submersible

BODC Sample Metadata Report for DI216_CTD_CTD21

Sample reference number Nominal collection volume(l) Bottle rosette position Bottle firing sequence number Minimum pressure sampled (dbar) Maximum pressure sampled (dbar) Depth of sampling point (m) Bottle type Sample quality flag Bottle reference Comments
553539   10.00      152.70  153.80  149.80 Lever Action Niskin Bottle No problem reported    
553540   10.00      103.20  104.00  100.60 Lever Action Niskin Bottle No problem reported    
553541   10.00       53.40   54.20   51.20 Lever Action Niskin Bottle No problem reported    
553542   10.00       49.80   50.50   47.60 Lever Action Niskin Bottle No problem reported    
553543   10.00       33.00   34.00   31.10 Lever Action Niskin Bottle No problem reported    
553544   10.00       13.20   14.00   11.40 Niskin bottle No problem reported    

Please note:the supplied parameters may not have been sampled from all the bottle firings described in the table above. Cross-match the Sample Reference Number above against the SAMPRFNM value in the data file to identify the relevant metadata.

Related Data Activity activities are detailed in Appendix 1

Cruise

Cruise Name D216
Departure Date 1995-08-26
Arrival Date 1995-09-12
Principal Scientist(s)Peter J Statham (University of Southampton Department of Oceanography)
Ship RRS Discovery

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

Appendix 1: DI216_CTD_CTD21

Related series for this Data Activity are presented in the table below. Further information can be found by following the appropriate links.

If you are interested in these series, please be aware we offer a multiple file download service. Should your credentials be insufficient for automatic download, the service also offers a referral to our Enquiries Officer who may be able to negotiate access.

Series IdentifierData CategoryStart date/timeStart positionCruise
2123173Water sample data1995-09-02 05:24:3048.5816 N, 13.32146 WRRS Discovery D216
2124397Water sample data1995-09-02 05:24:3048.5816 N, 13.32146 WRRS Discovery D216
2129457Water sample data1995-09-02 05:24:3048.5816 N, 13.32146 WRRS Discovery D216
1254789Water sample data1995-09-02 05:25:0048.5816 N, 13.32146 WRRS Discovery D216