Search the data

Metadata Report for BODC Series Reference Number 787385


Metadata Summary

Data Description

Data Category CTD or STD cast
Instrument Type
NameCategories
Neil Brown MK3 CTD  CTD; water temperature sensor; salinity sensor; dissolved gas sensors
SeaTech transmissometer  transmissometers
Sea-Bird SBE 13 Dissolved Oxygen Sensor  dissolved gas sensors
Chelsea Technologies Group Aquatracka fluorometer  fluorometers
Chelsea Technologies Group 2-pi PAR irradiance sensor  radiometers
Instrument Mounting lowered unmanned submersible
Originating Country United Kingdom
Originator Mr John Howarth
Originating Organization Proudman Oceanographic Laboratory (now National Oceanography Centre, Liverpool)
Processing Status banked
Online delivery of data Download available - Ocean Data View (ODV) format
Project(s) Provess
 

Data Identifiers

Originator's Identifier CTD12
BODC Series Reference 787385
 

Time Co-ordinates(UT)

Start Time (yyyy-mm-dd hh:mm) 1998-10-27 01:38
End Time (yyyy-mm-dd hh:mm) -
Nominal Cycle Interval 1.0 decibars
 

Spatial Co-ordinates

Latitude 59.32150 N ( 59° 19.3' N )
Longitude 1.04317 E ( 1° 2.6' E )
Positional Uncertainty 0.0 to 0.01 n.miles
Minimum Sensor or Sampling Depth 0.5 m
Maximum Sensor or Sampling Depth 97.55 m
Minimum Sensor or Sampling Height 5.35 m
Maximum Sensor or Sampling Height 102.4 m
Sea Floor Depth 102.9 m
Sea Floor Depth Source -
Sensor or Sampling Distribution Variable common depth - All sensors are grouped effectively at the same depth, but this depth varies significantly during the series
Sensor or Sampling Depth Datum Instantaneous - Depth measured below water line or instantaneous water body surface
Sea Floor Depth Datum Instantaneous - Depth measured below water line or instantaneous water body surface
 

Parameters

BODC CODERankUnitsTitle
ATTNMR011per metreAttenuation (red light wavelength) per unit length of the water body by 20 or 25cm path length transmissometer
CPHLPR011Milligrams per cubic metreConcentration of chlorophyll-a {chl-a CAS 479-61-8} per unit volume of the water body [particulate >unknown phase] by in-situ chlorophyll fluorometer
DOXYPR011Micromoles per litreConcentration of oxygen {O2 CAS 7782-44-7} per unit volume of the water body [dissolved plus reactive particulate phase] by in-situ Beckmann probe
FVLTAQ011VoltsRaw signal (voltage) of instrument output by in-situ Aquatracka chlorophyll fluorometer
IRRDPP011MicroEinsteins per square metre per secondDownwelling 2-pi scalar irradiance as photons of electromagnetic radiation (PAR wavelengths) in the water body by 2-pi scalar radiometer
OXYSBB011PercentSaturation of oxygen {O2 CAS 7782-44-7} in the water body [dissolved plus reactive particulate phase] by in-situ Beckmann probe and computation from concentration using Benson and Krause algorithm
POTMCV011Degrees CelsiusPotential temperature of the water body by computation using UNESCO 1983 algorithm
PRESPR011DecibarsPressure (spatial coordinate) exerted by the water body by profiling pressure sensor and correction to read zero at sea level
PSALCC011DimensionlessPractical salinity of the water body by CTD and computation using UNESCO 1983 algorithm and calibration against independent measurements
SIGTPR011Kilograms per cubic metreSigma-theta of the water body by CTD and computation from salinity and potential temperature using UNESCO algorithm
TEMPST011Degrees CelsiusTemperature of the water body by CTD or STD
TSEDTR011Milligrams per litreConcentration of suspended particulate material {SPM} per unit volume of the water body [particulate >unknown phase] by in-situ optical attenuance measurement and calibration against sample data

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

Sea Bird Electronics SBE13 Dissolved Oxygen Sensor

The SBE 13 was designed as an auxiliary sensor for Sea Bird SBE 9plus, but can fitted in custom instrumentation applications. When used with the SBE 9 Underwater Unit, a flow-through plenum improves the data quality, as the pumping water over the sensor membrane reduces the errors caused by oxygen depletion during the periods of slow or intermittent flushing and also reduces exposure to biofouling.

The output voltage is proportional to membrane current (oxygen current) and to the sensor element's membrane temperature (oxygen temperature), which is used for internal temperature compensation.

Two versions of the SBE 13 are available: the SBE 13Y uses a YSI polarographic element with replaceable membranes to provide in situ measurements up to 2000 m depth and the SBE 13B uses a Beckman polarographic element to provide in situ measurements up to 10500 m depth, depending on the sensor casing. This sensor includes a replaceable sealed electrolyte membrane cartridge.

The SBE 13 instrument has been out of production since 2001 and has been superseded by the SBE 43.

Specifications

Measurement range 0 to 15 mL L-1
Accuracy 0.1 mL L-1
Time response

2 s at 25°C

5 s at 0°C

Depth range

2000 m (SBE 13Y- housing in anodized aluminum)

6800 m (SBE 13B- housing in anodized aluminum)

105000 m (SBE 13B- housing in titanium)

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

Neil Brown MK3 CTD

The Neil Brown MK3 conductivity-temperature-depth (CTD) profiler consists of an integral unit containing pressure, temperature and conductivity sensors with an optional dissolved oxygen sensor in a pressure-hardened casing. The most widely used variant in the 1980s and 1990s was the MK3B. An upgrade to this, the MK3C, was developed to meet the requirements of the WOCE project.

The MK3C includes a low hysteresis, titanium strain gauge pressure transducer. The transducer temperature is measured separately, allowing correction for the effects of temperature on pressure measurements. The MK3C conductivity cell features a free flow, internal field design that eliminates ducted pumping and is not affected by external metallic objects such as guard cages and external sensors.

Additional optional sensors include pH and a pressure-temperature fluorometer. The instrument is no longer in production, but is supported (repair and calibration) by General Oceanics.

Specifications

These specification apply to the MK3C version.

Pressure Temperature Conductivity
Range

6500 m

3200 m (optional)

-3 to 32°C 1 to 6.5 S cm-1
Accuracy

0.0015% FS

0.03% FS < 1 msec

0.0005°C

0.003°C < 30 msec

0.0001 S cm-1

0.0003 S cm-1 < 30 msec

Further details can be found in the specification sheet.

Aquatracka fluorometer

The Chelsea Instruments Aquatracka is a logarithmic response fluorometer. It uses a pulsed (5.5 Hz) xenon light source discharging between 320 and 800 nm through a blue filter with a peak transmission of 420 nm and a bandwidth at half maximum of 100 nm. A red filter with sharp cut off, 10% transmission at 664 nm and 678 nm, is used to pass chlorophyll-a fluorescence to the sample photodiode.

The instrument may be deployed either in a through-flow tank, on a CTD frame or moored with a data logging package.

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

Chelsea Technologies Photosynthetically Active Radiation (PAR) Irradiance Sensor

This sensor was originally designed to assist the study of marine photosynthesis. With the use of logarithmic amplication, the sensor covers a range of 6 orders of magnitude, which avoids setting up the sensor range for the expected signal level for different ambient conditions.

The sensor consists of a hollow PTFE 2-pi collector supported by a clear acetal dome diverting light to a filter and photodiode from which a cosine response is obtained. The sensor can be used in moorings, profiling or deployed in towed vehicles and can measure both upwelling and downwelling light.

Specifications

Operation depth 1000 m
Range 2000 to 0.002 µE m-2 s-1
Angular Detection Range ± 130° from normal incidence
Relative Spectral Sensitivity

flat to ± 3% from 450 to 700 nm

down 8% of 400 nm and 36% at 350 nm

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

SeaTech Transmissometer

Introduction

The transmissometer is designed to accurately measure the the amount of light transmitted by a modulated Light Emitting Diode (LED) through a fixed-length in-situ water column to a synchronous detector.

Specifications

  • Water path length: 5 cm (for use in turbid waters) to 1 m (for use in clear ocean waters).
  • Beam diameter: 15 mm
  • Transmitted beam collimation: <3 milliradians
  • Receiver acceptance angle (in water): <18 milliradians
  • Light source wavelength: usually (but not exclusively) 660 nm (red light)

Notes

The instrument can be interfaced to Aanderaa RCM7 current meters. This is achieved by fitting the transmissometer in a slot cut into a customized RCM4-type vane.

A red LED (660 nm) is used for general applications looking at water column sediment load. However, green or blue LEDs can be fitted for specilised optics applications. The light source used is identified by the BODC parameter code.

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

RRS Challenger 140 CTD Data Documentation

Cruise Principal Scientist

John Howarth, Proudman Oceanographic Laboratory (POL), Merseyside, UK.

Data Originators

British Oceanographic Data Centre, POL, Merseyside, UK.
Research Vessel Services, SOC, Southampton, UK.

Content of data series

Parameter Unit Parameter code Number of stations Comments
Pressure db PRESPR01 60 none
Salinity PSU-78 PSALCC01 60 none
Temperature deg. C TEMPST01 60 none
Potential temperature (UNESCO) deg. C POTMCV01 60 none
Sigma-theta (UNESCO SVAN) kg m-3 SIGTPR01 60 none
Chlorophyll a µg l-1 CPHLPR01 42 calibrated from fluorometer voltages caution (see text)
Raw fluorometer voltages volts FVLTAQ01 60 none
Optical attenuance m-1 ATTNMR01 60 none
Total suspended sediment mg l-1 TSEDTR01 60 calibrated from attenuance caution (see text)
Dissolved oxygen µmol l-1 DOXYPR01 31 caution (see text)
Oxygen saturation percent OXYSBB01 31 caution (see text)
Downwelling PAR µE m-2 s-1 IRRDPP01 60 none
Upwelling PAR µE m-2 s-1 IRRUPP01 60 none

Instrumentation and data processing by originator

CTD unit and auxiliary sensors

RVS Neil Brown Mk3B CTD incorporating a pressure sensor, a conductivity cell, a platinum resistence thermometer, a 20 cm pathlength SeaTech transmissometer (660 nm), a Mk II Aquatracka fluorometer, two 2PI PAR light meters for upwelling and downwelling irradiance and a Beckman dissolved oxygen sensor fed by a Seabird 5T submersible pump.

Changes of sensors during the cruise

  • the transmissometer T-1022D was spiking intermittently and moisture in the slip ring assembly was suspected. It was replaced by transmissometer T-1019D for cast 03 but the noise persisted. T-1022D was re-installed on the CTD frame. Further attempts to resolve the problem were unsuccessful.
  • the fluorometer SA-226 was replaced by fluorometer SA3-254 between casts 04 and 05 because of the presence of unusually high noise and spikes in the fluorescence profiles.

Data acquisition

The CTD was first lowered down to a depth of approx. 10 m where it was left for a few minutes before being brought back to just below sea surface. This was necessary to activate the SeaBird pump. It was then lowered continuously at 0.5 to 1 m s-1 to the closest comfortable proximity to the sea floor. The upcast was done in stages between bottle firing depths.

Data were logged by the RVS ABC data logging system. Output channels from the deck were logged at 32 Hz by a microprocessor interface (Level A) which passed time-stamped averaged cycles at 1Hz to a Sun workstation (Level C) via a buffering system (Level B).

On-board data processing

The raw data (ADC counts) were converted into engineering units (volts for PAR meters, for fluorometers and transmissometers; ml/l for oxygen; mmho/cm for conductivity; °C for temperature; decibars for pressure) by the application of laboratory determined calibrations. Salinity (Practical Salinity Units as defined in Fofonoff and Millard 1983) was calculated from the conductivity ratios (conductivity/42.914) and a time-lagged temperature using the function described in UNESCO Report 37 (1981). PAR volts were converted to µWatts cm-2

The data set was submitted to BODC in this form on Quarter Inch Cartridge tapes in RVS internal format for post-cruise processing and data banking.

Sampling device

The CTD unit was protected by a metallic frame. A General Oceanic rosette sampler equipped with twelve 30-litre Niskin water bottles was fitted above the frame. The base of the bottles was at 0.75 metres above the pressure head and their tops at 1.55 m above it. One bottle was fitted with a holder for twin digital reversing thermometers mounted 1.40 metres above the CTD temperature sensor.

Above the rosette was a PML 2PI PAR (photosynthetically available radiation) sensor pointing upwards to measure downwelling irradiance. A second 2PI PAR sensor, pointing downwards, was fitted to the bottom of the cage to measure upwelling irradiance.

No account has been taken of rig geometry in the compilation of the CTD data set. However, all water bottle sampling depths (and digital thermometer readings) have been corrected for rig geometry and represent the true position of the midpoint of the water bottle in the water column.

BODC post-cruise processing and screening

Reformatting

The data were converted into BODC internal format (PXF) to allow use of in-house software tools notably the workstation graphics editor SERPLO. In addition to reformatting, the transfer program applied the following modifications to the data:

  • dissolved oxygen was converted from ml l-1 to µmol l-1 by multiplying the values by 44.66.
  • transmissometer voltages were corrected to the manufacturer's specified voltage ratio by using transmissometer air readings taken during the cruise (see details in 'Calibration' paragraph). The voltages were then converted to percentage transmission by multiplying them by a factor of 20. Conversion to attenuance was made using the following algorithms:
% transmission= Volts * 20 * Va / Vb (1)
attenuance (m-1) = -1 / PL * loge (% transmission / 100) (2)

where Va is the manufacturer's air reading for this instrument, Vb is the average of the air readings carried out during the cruise and PL is the transmissometer pathlength in metres (0.20 m).

  • light units were re-converted from µWatts cm-2 to Volts to allow for the application of BODC's calibration software.

Screening

Reformatted CTD data were transferred onto a high-speed graphics workstation. Using custom in-house graphics editor SERPLO, downcasts and upcasts were differentiated and the limits of the downcasts and upcasts were manually flagged. If present, spikes and suspicious data on all the downcast channels were manually flagged. No data values were edited or deleted; flagging was achieved by modification of the associated quality control flag to 'M' for suspicious values and 'N' for null.

The pressure ranges over which the bottle samples had been collected were logged by manual interaction with the software. Usually, the marked reaction of the oxygen sensor to the bottle firing sequence was used to determine this. These pressure ranges were subsequently used, in conjunction with a geometrical correction for the position of the water bottles with respect to the CTD pressure transducer, to determine the pressure range of data to be averaged for calibration values.

Banking

Once screened on the workstation, the CTD downcasts were loaded into a database under the ORACLE Relational Database Management System.

Calibration

With the exception of pressure, calibrations were done by comparison of CTD data against measurements made on water bottle samples or from the reversing thermometers mounted on the water bottles as in the case of temperature. In general, values were averaged from the CTD downcasts but where visual inspection of the data showed significant hysteresis values were manually extracted from the CTD upcasts.

  • Pressure: the pressure offset was determined by looking at the pressure values recorded when the CTD was logging in the air (readily apparent from the conductivity channel). Only casts with no spike in the pressure channel were considered for the determination of the pressure offset. The following correction was applied
Pcorr= P - 1.13 (standard deviation 0.36 db)
  • Temperature: the CTD temperature was compared with readings from the digital reversing thermometers attached to the water bottles (data originator: J. Benson, RVS, Southampton, UK). A significant offset was observed between the Neil Brown CTD thermometer and the temperature readings from the two digital thermometers. Since this offset was consistent throughout the cruise, the following correction was applied:
Tcorr = T + 0.022 (standard deviation 0.002)
  • Salinity: salinity was calibrated against water bottle samples measured on the Guildline 55358 AutoLab Salinometer during the cruise (data originator: J. Benson, RVS, UK). Samples were collected in glass bottles filled to just below the neck and sealed with plastic stoppers. Batches of samples were left for at least 24 hours to reach thermal equilibrium in the laboratory containing the salinometer before analysis.

A significant offset in the difference between CTD-salinity and salinometer-salinity was observed between the first leg (24-28 Oct.) and second leg (1-7 Nov.) of the cruise. As a result two different corrections have been applied to the following groups of CTD casts:

CTD01 to CTD18: Scorr= S - 0.030 (standard deviation 0.003)
CTD19 to CTD60: Scorr = S - 0.039 (standard deviation 0.002)

Upwelling and downwelling irradiance: the PAR voltages were converted to W m-2 using the following equations determined in August 1995 and supplied by RVS:

Downwelling (#12): PAR (W m-2) = exp (-4.92*volts + 6.506)/100
Upwelling (#11): PAR (W m-2) = exp (-5.00*volts + 6.536)/100

The data were then converted from W m-2 into µE m-2 s-1 (22/12/1998) by applying a multiplication factor of 3.75. This factor is derived from an empirical calibration of the 2PI PAR sensors.

  • Optical attenuance and suspended matter: the air correction applied was based on the averaged air readings obtained during the cruise and on the manufacturer's air reading for the instrument used. The readings associated with the two transmissometers used during the cruise were as follows:
T-1022-D (all casts except CTD03):
manufacturer's air reading = 4.662 volts
air reading = 4.656 volts
blocked light path reading = 0.000 volts
T-1019-D (CTD03):
manufacturer's air reading = 4.682 volts
air reading not available (used manufacturer's air reading)
blocked light path reading = 0.002 volts

The air correction was applied during the transfer of the ASCII data into PXF (see above). The data stored in the database are therefore calibrated.

  • Total suspended particulate matter concentration (TSED) was estimated at the University of Wales, Bangor, by linear regression of the concentration of total suspended particulate matter as measured on water samples by gravimetry and attenuance (ATTN) as measured by the CTD transmissometer at the time of sample collection. The resulting calibration equation is:
TSED (mg l-1) = (ATTN - 0.39557) / 0.46891, R2=0.373, n=62
  • Chlorophyll: the voltage of the CTD fluorometer was very unstable during this cruise. During screening it became obvious that the data could be distributed into three groups:
  • a first group of 24 profiles characterised by a low voltage signal (casts 04-05, 13-15, 17-19, 21, 28, 30- 32, 37-38, 43, 47-48, 50, 52-56).
  • a second group of 18 profiles characterised by a high voltage signal (casts 06-12, 25, 34, 36, 39, 41- 42, 45, 49, 58-60).
  • a third group of 18 profiles during which the signal jumped from low to high voltage (casts 01-03, 16, 20, 22-24, 26-27, 29, 33, 35, 40, 44, 46, 51, 57).

For the third group the noise in the data was such that it was deemed impossible to calibrate the data. The whole fluorescence profile was therefore flagged suspect and no chlorophyll concentration was derived.

For the remaining profiles, the calibration dataset was composed of 49 measurements of extracted chlorophyll (data originator: K. Jones, DML, UK) of which 28 were associated with low voltages fluorometer output and 21 with high voltages fluorometer output. The range of chlorophyll concentration was quite low in both groups ranging from 0 to 0.54 µg l-1 in the low voltage group and 0 to 0.57 µg l-1 in the high voltage group. The calibration equations applied are as follows:

Low voltage group: Chl = exp (12.59 FV - 10.54), R2=0.278, n=15
High voltage group: Chl = exp (5.72 FV - 10.02), R2=0.744, n=14

where Chl = predicted chlorophyll a concentration in µg l-1 and FV= CTD fluorometer voltage. Note that null values for chlorophyll concentration had to be excluded in order to calculate the logarithmic fit. Residuals from the regressions ranged from -0.25 to +0.29 µg l-1 for the first group and from -0.23 to +0.25 µg l-1for the second. Both residuals and predicted values were examined graphically for skewness. The distribution of the regression residuals were also examined against sample depths and in situ irradiance but no significant trends were observed.

  • Oxygen: problems were observed with the oxygen record on a number of profiles probably due to a malfunction of the oxygen pump. Good, reliable data were only observed from casts 04 to 13. For casts 01 to 03 the records were very unstable and the entire profiles were flagged as suspect. For casts 14 to 18 the entire profile was null. After cast 18 the oxygen pump functioned very sporadically and a number of profiles were eliminated: casts 20-21, 25-30, 34-36, 40-49, 52, 54, 58-60. For the other profiles, although the relative changes in oxygen concentration with depth look real, the oxygen concentration and oxygen saturation values were unrealistically high. Oxygen profiles for the following casts were therefore flagged as suspect: 19, 22-24, 31-32, 37-38, 50-51, 53, 55-57.

Oxygen concentration measurements by Winkler titration were performed on samples taken from eight depths on casts 02, 05 and 14 (data originator: K. Jones, DML, UK). Because of the problems encountered with the CTD oxygen probe on casts 02 and 14 calibration could only be derived using data from cast 05. The calibration equation derived is as follows:

Oxygen= 4.20 CTD_oxygen - 227.70, R2= 0.889, n=8

Considering that this calibration was derived from one profile only, users are advised to use the calibrated oxygen CTD data with caution.

Comments on data quality

  • Salinity: suspect flags were applied to spikes observed on the pycnocline and to loops associated with the ship's motion. Malfunction of the conductivity cell for casts 01 and 03 resulted in bad salinity values being recorded on the downcast (salinity offset between downcast and upcast values was 1.5 PSU for cast 01 and 0.5 PSU for casts 03). A correction was applied to the banked salinity data based on values observed during the upcast. These data were flagged 'R'.
  • Fluorometer: as detailed above the fluorometer malfunctioned during the cruise and full calibration procedure was only carried out on 42 of the 60 casts.
  • Oxygen probe: the oxygen probe functioned intermittently during the cruise: 29 profiles were discarded because the probe recorded either wrong data or showed no signal. Oxygen profiles for casts 21 to 60 were generally of poor quality and post-calibration concentrations and saturation values tended to be unrealistically high. These data should be treated with extreme caution. On the other hand, oxygen profiles from casts 04 to 13 were of better quality and post-calibration values compared well with oxygen concentration measured on water samples.

Project Information

PROcesses of Vertical Exchange in Shelf Seas (PROVESS)

Introduction

PROVESS was an interdisciplinary study of the vertical fluxes of properties through the water column and the surface and bottom boundary layers. The project was funded by the European Community MAST-III programme (MAS3-CT97- 0159) and ran from March 1998 to May 2001.

Scientific Rationale

PROVESS was based on the integration of experimental, theoretical and modelling studies with the aim of improving understanding and quantification of vertical exchange processes in the water column, in particular in the surface and benthic boundary layers and across the> pycnocline. PROVESS also explored mechanisms of physical-biological coupling in which vertical exchanges and turbulence significantly affect the environmental conditions experienced by the biota with particular reference to aggregation, flocculation, sedimentation and trophic interactions.

Fieldwork

The experimental phase of the project was carried out at two contrasting sites in the North Sea: the northern North Sea site (NNS) and the southern North Sea site (SNS).

The two sites had the following characteristics:

SNS NNS
Position 52° 15.0' N, 4° 17.0' E 59° 20.0' E, 1° 00.0' E
Time of year April-May September-November
Water depth (m) 16 100
M2 max amplitude (m s-1) 0.75 0.15
Max current (m s-1) 1.0 0.6
Delta T (deg C) mixed 7-1
Thermocline depth (m) mixed 35-100
Delta S 1 small
Halocline depth (m) 5-10 cf. thermocline depth
Max wind speed (m s-1) 20 25
Max wave height (m) 5 10
Max wave period (s) 8 10
Internal motion No Yes
Sediment muddy-sand muddy-sand
Biology eutrophic oligotrophic

At both locations measurements were concentrated at a central position with additional measurements being made to estimate horizontal gradients. Moored instruments (including current meters, temperature and pressure sensors, fluorometers, transmissometers, nutrient analysers and meteorological sensors) were deployed between 7 September and 5 November 1998 at the NNS and between 29 March and 25 May 1999 at the SNS. Each experiment was supported by intensive measurement series made from oceanographic ships and involving turbulence dissipation profiler CTD, particle size profilers, optical profilers, benthic sampling and water bottle sampling.

Details of the cruises were as follows:

Site Ship
(nationality)
Cruise
Mnemonic
Date
NNS Valdivia (GER) VA174 5 - 17 Sep 1998
  Dana (DK) D1198 14 - 26 Oct 1998
  Pelagia (NL) PE125 19 - 30 Oct 1998
  Challenger (UK) CH140 22 Oct - 9 Nov 1998
SNS Pelagia (NL) PE135 29 Mar - 9 Apr 1999
  Mitra (NL) MT0499 19 - 30 Apr 1999
  Belgica (BE) BG9912 17 - 21 May 1999

Data Activity or Cruise Information

Cruise

Cruise Name CH140 (PROVESS N-4)
Departure Date 1998-10-21
Arrival Date 1998-11-11
Principal Scientist(s)M John Howarth (Proudman Oceanographic Laboratory)
Ship RRS Challenger

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