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Metadata Report for BODC Series Reference Number 2122089


Metadata Summary

Data Description

Data Category Water sample data
Instrument Type
NameCategories
Lever Action Niskin Bottle  discrete water samplers
Becton Dickinson FACSort Flow Cytometer  flow cytometers
Instrument Mounting lowered unmanned submersible
Originating Country United Kingdom
Originator Dr Glen Tarran
Originating Organization Plymouth Marine Laboratory
Processing Status banked
Online delivery of data Download available - Ocean Data View (ODV) format
Project(s) UKSOLAS
 

Data Identifiers

Originator's Identifier D325_CTD_AFCX_104:CTD_C039_TIT
BODC Series Reference 2122089
 

Time Co-ordinates(UT)

Start Time (yyyy-mm-dd hh:mm) 2007-11-28 06:52
End Time (yyyy-mm-dd hh:mm) -
Nominal Cycle Interval -
 

Spatial Co-ordinates

Latitude 16.00555 N ( 16° 0.3' N )
Longitude 23.66433 W ( 23° 39.9' W )
Positional Uncertainty 0.05 to 0.1 n.miles
Minimum Sensor or Sampling Depth 2.1 m
Maximum Sensor or Sampling Depth 56.0 m
Minimum Sensor or Sampling Height 3599.4 m
Maximum Sensor or Sampling Height 3653.3 m
Sea Floor Depth 3655.4 m
Sea Floor Depth Source PEVENT
Sensor or Sampling Distribution Unspecified -
Sensor or Sampling Depth Datum Unspecified -
Sea Floor Depth Datum Instantaneous - Depth measured below water line or instantaneous water body surface
 

Parameters

BODC CODERankUnitsTitle
ADEPZZ011MetresDepth (spatial coordinate) relative to water surface in the water body
BOTTFLAG1Not applicableSampling process quality flag (BODC C22)
C804B6A61Number per millilitreAbundance of bacteria (ITIS: 202421: WoRMS 6) [Subgroup: heterotrophic; low nucleic acid cell content] per unit volume of the water body by flow cytometry
FIRSEQID1DimensionlessBottle firing sequence number
J79A05961Number per millilitreAbundance of Cryptophyceae (ITIS: 10598: WoRMS 17639) per unit volume of the water body by flow cytometry
P18318A91Number per millilitreAbundance of bacteria (ITIS: 202421: WoRMS 6) [Subgroup: heterotrophic; high nucleic acid cell content] per unit volume of the water body by flow cytometry
P490A00Z1Number per millilitreAbundance of Prymnesiophyceae (ITIS: 2135: WoRMS 115057) [Subgroup: coccolithophores] per unit volume of the water body by flow cytometry
P700A90Z1Number per millilitreAbundance of Synechococcus (ITIS: 773: WoRMS 160572) per unit volume of the water body by flow cytometry
P701A90Z1Number per millilitreAbundance of Prochlorococcus (ITIS: 610076: WoRMS 345515) per unit volume of the water body by flow cytometry
PU00A02A1Number per millilitreAbundance of eukaryote picophytoplankton per unit volume of the water body by flow cytometry
ROSPOSID1DimensionlessBottle rosette position identifier
SAMPRFNM1DimensionlessSample reference number
X726A86B1Number per millilitreAbundance of nanoeukaryotic cells [Size: 2-12um] per unit volume of the water body by flow cytometry

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

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

Becton Dickinson FACSort Flow Cytometer

The Becton Dickinson FACSort Flow Cytometer is a benchtop, five-detector, flow cytometer that is designed to analyse cells as they travel, one by one, in a moving fluid stream, through a focused, air-cooled, argon-ion laser beam. Samples are introduced through a stainless steel injection tube equipped with an outer droplet containment sleeve. As the cell passes through the laser, a mechanical catcher tube located in the upper portion of the flow cell, moves in and out of the sample stream to collect desired cells at a rate of up to 300 per second. The physical characteristics of the cells, which pertain to how the cell scatters the laser light and emits fluorescence are then analysed. This provides information about the cell's size, internal complexity and relative fluorescence intensity. Up to five parameters can be measured at once by the FACSort including forward light scatter, side light scatter, three fluorescence parameters, pulse height and width of each fluorescence parameter. FACSort can be operated with any Macintosh computer, where the information is output to. The FACSort system includes CELLQuest software for acquisition and analysis and FACSComp software for daily setup and quality control.

Droplet formation of sheath fluid as it backflows from the injection tube is eliminated by the use of the containment sleeve in conjunction with a vacuum pump. Fluid controls allow the user to select the fluidics mode and sample flow rate. As a mechanical device is used to sort cells, no side streams are formed so aerosol formation is completely eliminated. The laser alignment and stream velocity are fixed so the time it takes for desired cells to reach the catcher tube is constant so no setup calculations are required. As no optical alignment is required, daily setup can be performed quickly and consistently. Between one and three cell collection tubes can be installed and the instrument will automatically determine the maximum volume of sample to collect.

Specifications

Excitation: Laser Cyonics 15 mW, 488 nm, air-cooled, argon-ion laser (Class I). Life expectancy >5000 hours.
Excitation: Beam Geometry Prismatic expander and spherical lens provide 20 x 64 µm elliptical beam.
Optics: Alignment Fixed, no user adjustments necessary or available.
Optics: Dichroics 560/22.5 ° (blue/orange-red); 640 LP (orange/red)
Optics: Filters FL1: 530/30; FL2: 585/42; FL3: 650 LP
Photomultipliers FL1, FL2, FL3: R1477, SSC: 1P28
Fluidics: Flow Rates Three selectable flow rates: LO (12 µL ±3 µL/min); MED (35 µL ±5 µL/min); HI (60 µL ±7 µL/min)
Fluidics: Quartz Cuvette Internal cross-section is rectangular 430 x 180 µm. External surfaces are anti reflection coated.
Fluidics: Air Pressure Internal air pump provides sheath pressure of 4.5 psig and sample pressures of 4.6, 4.8 and 5.0 psig.
Electronics: Parameters Seven data channels available for acquisition: FSC, SSC, FL1, FL2, FL3, FLX-W, FLX-A (X=DDM parameter)
Electronics: Acquisition speed 20 µs approximate processing time while sorting; acquires up to 10000 cells/sec.
Electronics: Sort rate 300 cells/sec maximum in Single Cell sort mode.
Signal Processing: measurement resolution 256 or 1024 channels on all 5 parameters (Seven when acquiring with DDM).
Signal Processing: signal modes Any combination of logarithmic or linear selections for each detector.
Signal Processing: Dynamic range Four decades are provided by logarithmic amplifiers for each of the 5 parameters.
Signal Processing: Fluorescence sensitivity 1000 molecules of equivalent soluble fluorescein.

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

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.

Flow Cytometry CTD bottle data for UK SOLAS cruise Discovery D325 (INSPIRE)

Originator's Data Acquisition and Analysis

Fresh seawater samples were collected from CTD casts into clean 250 mL polycarbonate bottles from both the stainless steel (20 x 24 L bottles) and titanium (20 x 10 L bottles) CTD/Rossette systems. Samples were stored in a refrigerator until analysed (less than 1 hour). 3 mL samples were used for immediate flow cytometric analysis to characterise and enumerate prochlorophytes, cyanobacteria, pico-eukaryotes and nanophytoplankton based on their light scattering and fluorescence properties. Analysis was conducted using a Becton Dickinson FACSort flow cytometer.

BODC Data Processing Procedures

Data were received by BODC in Microsoft Excel spreadsheet format; one file containing all flow cytometry data collected from CTD bottles throughout the cruise (SolasInspireAFCBODC.xls). The following metadata fields were also included in the spreadsheet: date, julian day, time on deck GMT, site, trophic type, cast, lat N, long W, sample, niskin bottle # and depth.

Parameter codes defined in the BODC parameter dictionary were mapped to the variables as follows:

Originators Parameter Units Description BODC Parameter Code Units Comments
SYN cells per ml Cell abundance of Synechoccus sp. per unit volume of seawater P700A90Z cells per ml n/a
PRO cells per ml Cell abundance of Prochlorococcus sp. per unit volume of seawater P701A90Z cells per ml n/a
PEUK cells per ml Cell abundance of pikoeukaryote phytoplankton (<2 µm) per unit volume of seawater PU00A02A cells per ml n/a
NEUK cells per ml Cell abundance of nanoeukaryote phytoplankton (~2-12 µm) per unit volume of seawater X726A86B cells per ml n/a
COCCO cells per ml Cell abundance of coccolithophores per unit volume of seawater P490A00Z cells per ml n/a
CRYP cells per ml Cell abundance of cryptophytes per unit volume of seawater J79A0596 cells per ml n/a
BacHNA cells per ml Cell abundance of heterotrophic bacteria - high nucleic acid content per unit volume of seawater P18318A9 cells per ml n/a
BacLNA cells per ml Cell abundance of heterotrophic bacteria - low nucleic acid content per unit volume of seawater C804B6A6 cells per ml n/a

The data were then banked according to BODC standard procedures for sample data. Once tagged with the appropriate parameter code and, if necessary, converted to BODC standard unit for that parameter, the data are loaded into BODC Samples Database. In this process, sample metadata are checked against information held in the database. Discrepancies are investigated and, when necessary cross-checked with the data originator prior to correction.

Data Quality Report

No advice concerning the data quality was received by BODC from the originator. During BODC processing no standout data points were noted.


Project Information

UK Surface Ocean Lower Atmosphere Study

The UK Surface Ocean Lower Atmosphere Study (UK SOLAS) is the UK's contribution to the international SOLAS programme.

UK SOLAS formed interdisciplinary teams to address three primary aims

  • To determine the mechanisms controlling rates of chemical transfer and improve estimates of chemical exchanges
  • To evaluate the impact of these exchanges on the biogeochemistry of the surface ocean and lower atmosphere and on feedbacks between the ocean and atmosphere
  • To quantify the impacts of these boundary layer processes on the global climate system

UK SOLAS started in 2003, to run for seven years. The programme was funded by the Natural Environment Research Council.

Funded projects

In total, 19 projects have been funded by UK SOLAS, over four funding rounds.

Project Title Short Title Principal Investigator
Impact of atmospheric dust derived material and nutrient inputs on near-surface plankton microbiota in the tropical North Atlantic Dust Eric Achterberg
The role and effects of photoprotective compounds in marine plankton - Steve Archer
Field observations of sea spray, gas fluxes and whitecaps SEASAW Ian Brooks
Factors influencing the biogeochemistry of iodine in the marine environment - Lucy Carpenter
Global model of aerosol processes - effects of aerosol in the marine atmospheric boundary layer GLOMAP Ken Carslaw
Ecological controls on fluxes of dimethyl sulphide (DMS) to the atmosphere - David Green
Dust outflow and deposition to the ocean DODO Ellie Highwood
Investigation of near surface production of iodocarbons - rates and exchanges INSPIRE Gill Malin
Reactive halogens in the marine boundary layer RHaMBLe Gordon McFiggans
The role of bacterioneuston in determining trace gas exchange rates - Colin Murrell
Measuring methanol in sea water and investigating its sources and sinks in the marine environment - Phil Nightingale
The impact of coastal upwellings on air-sea exchange of climatically important gases ICON Carol Robinson
The Deep Ocean Gas Exchange Experiment DOGEE Rob Upstill-Goddard
High wind air-sea exchanges HiWASE Margaret Yelland
Aerosol characterisation and modelling in the marine environment ACMME James Allan
3D simulation of dimethyl sulphide (DMS) in the north east Atlantic - Icarus Allen
Processes affecting the chemistry and bioavailability of dust borne iron - Michael Krom
The chemical structure of the lowermost atmosphere - Alastair Lewis
Factors influencing the oxidative chemistry of the marine boundary layer - Paul Monks

UK SOLAS has also supported ten tied studentships, and two CASE studentships.

Fieldwork

UK SOLAS fieldwork has included eight dedicated research cruises in the North Atlantic Ocean. Continuous measurements were made aboard aboard the Norwegian weather ship, Polarfront, until her decommission in 2009. Time series have been established at the SOLAS Cape Verde Observatory, and at the Plymouth Marine Laboratory L4 station. Experiments have taken place at the Bergen mesocosm facility.

A series of collaborative aircraft campaigns have added complementary atmospheric data. These campaigns were funded by UK SOLAS, African Monsoon Multidisciplinary Analyses (AMMA-UK), Dust and Biomass Experiment (DABEX) and the Facility for Airborne Atmospheric Measurements (FAAM).

Weblink: http://www.nerc.ac.uk/research/programmes/solas/


Data Activity or Cruise Information

Data Activity

Start Date (yyyy-mm-dd) 2007-11-28
End Date (yyyy-mm-dd) 2007-11-28
Organization Undertaking ActivityUniversity of East Anglia School of Environmental Sciences
Country of OrganizationUnited Kingdom
Originator's Data Activity IdentifierD325_CTD_CTD_C039_TIT
Platform Categorylowered unmanned submersible

BODC Sample Metadata Report for D325_CTD_CTD_C039_TIT

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
187396   10.00 1 1  202.90  203.50  201.90 Lever Action Niskin Bottle No problem reported    
187397   10.00 13 2  202.60  203.50  201.70 Lever Action Niskin Bottle No problem reported    
187398   10.00 14 3  101.80  102.40  101.40 Lever Action Niskin Bottle No problem reported    
187399   10.00 15 4   66.20   66.70   66.00 Lever Action Niskin Bottle No problem reported    
187400   10.00 16 5   55.80   56.90   56.00 Lever Action Niskin Bottle No problem reported    
187401   10.00 17 6   51.10   51.80   51.10 Lever Action Niskin Bottle No problem reported    
187402   10.00 18 7   42.50   43.90   42.90 Lever Action Niskin Bottle No problem reported    
187403   10.00 19 8   35.90   36.80   36.10 Lever Action Niskin Bottle No problem reported    
187404   10.00 20 9   29.80   30.50   29.90 Lever Action Niskin Bottle No problem reported    
187405   10.00 21 10   18.80   19.50   19.00 Lever Action Niskin Bottle No problem reported    
187406   10.00 22 11   12.70   13.40   12.90 Lever Action Niskin Bottle No problem reported    
187407   10.00 23 12    8.10    8.50    8.20 Lever Action Niskin Bottle No problem reported    
187408   10.00 2 13    8.00    9.00    8.40 Lever Action Niskin Bottle No problem reported    
187409   10.00 3 14    8.20    8.70    8.40 Lever Action Niskin Bottle No problem reported    
187410   10.00 4 15    8.20    8.70    8.40 Lever Action Niskin Bottle No problem reported    
187411   10.00 5 16    7.90    9.10    8.40 Lever Action Niskin Bottle No problem reported    
187412   10.00 6 17    7.70    8.60    8.10 Lever Action Niskin Bottle No problem reported    
187413   10.00 7 18    7.80    8.90    8.30 Lever Action Niskin Bottle No problem reported    
187414   10.00 8 19    8.00    8.50    8.20 Lever Action Niskin Bottle No problem reported    
187415   10.00 9 20    8.00    8.90    8.40 Lever Action Niskin Bottle No problem reported    
187416   10.00 10 21    1.70    2.90    2.20 Lever Action Niskin Bottle No problem reported    
187417   10.00 11 22    1.50    3.00    2.20 Lever Action Niskin Bottle No problem reported    
187418   10.00 12 23    1.70    2.50    2.00 Lever Action Niskin Bottle No problem reported    
187419   10.00 24 24    1.60    2.80    2.10 Lever Action 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 D325
Departure Date 2007-11-13
Arrival Date 2007-12-18
Principal Scientist(s)Gill Malin (University of East Anglia School of Environmental Sciences)
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: D325_CTD_CTD_C039_TIT

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
1348158Water sample data2007-11-28 06:52:0016.00555 N, 23.66433 WRRS Discovery D325
1658605Water sample data2007-11-28 06:52:0016.00555 N, 23.66433 WRRS Discovery D325