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SurfaceFe

Data Object Fe - Surface
contact PIs:
name        title
Dr Andrew R Bowie         Principal Investigator
Dr Russell D. Frew         Co-Principal Investigator
Dr Doug Mackie         Contact

Dataset description

SOIREE Surface Fe Data

Comments preserved from the original file:
SOIREE Surface Fe underway data

Author: Andrew R. Bowie (University of Plymouth and Plymouth Marine Laboratory)
Dept. of Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA, United Kingdom
Tel. +44 1752 233128, Fax +44 1752 233035, E-mail abowie@plymouth.ac.uk

SOIREE Fe data used in the preparation of the manuscript:
Bowie et al. (2001), The Fate of Added Iron during a Mesoscale Fertilisation Experiment in the Southern Ocean

This data was prepared by Andrew Bowie, whom the ownership rests with.
The data is for use for SOIREE participants only for research purposes.
Before using this data in any presentation or printed publication, please
contact the author and include full acknowledgements. All enquiries regarding
the sampling, analysis and data preparation can be directed to the address above.

Notes
1. Dissolved iron (DFe) underway data (nM)
2. All surface Fe analyses were performed using a flow injection - chemiluminescence
   (FI-CL) technique based on the luminol reaction using dissolved oxygen as the oxidant
   (Bowie et al., 1998)
3. All underway samples taken torpedo fish towed at 0.5-1 m below the surface
4. The detection limit of the FI-CL method was 0.04 nM
5. The analytical blank varied between 0.09 and 0.24 nM over 13 d with a mean standard deviation of 0.013 nM
6. Contamination (suspected to be from the ship itself) resulted in a practical limit
   of detection for the underway mapping of 0.10-0.20 nM, which was monitored daily
7. Out-of-patch locations determined by absence of SF6 signal.
   Nevertheless, continuous tracking between high Fe within patch and
   almost two orders lower Fe out of patch may lead to memory effect contamination of the
   low values for out of patch. Therefore rejections of 61 suspect out of patch "contaminated" samples
8. A '<' symbol indicates that the concentration was below the practical limit of detection
9. The timing of samples collected from the underway system were adjusted for lag time delays
   due to surface water pumping and analysis (4.0-6.5 min)
10. Decimal time is given as days in February 1999 (GMT), with 1 February 1999 0:00 = 1.0000
11. Latitudes and longitudes are taken from the DAS on RV Tangaroa (no Lagrangian correction)
12. Each worksheet corresponds to one mapping session

References:
Bowie, A.R., Achterberg, E.P., Mantoura, R.F.C., Worsfold, P.J., 1998.
Determination of sub-nanomolar levels of iron in seawater using flow injection
with chemiluminescence detection. Analytica Chimica Acta 361, 189-200.

Bowie, A.R., Maldonado, M.T., Frew, R.D., Croot P.L., Achterberg, E.A., Mantoura,
R.F.C., Worsfold, P.J., Law, C.S., Boyd P.W., The Fate of Added Iron during a
Mesoscale Fertilisation Experiment in the Southern Ocean, Deep-Sea Research II (2001),
SOIREE special issue, in the press.

Note
Values in brackets ('[ ]') were suspected to be contaminated

Data from original Pre-release Site Survey Notes columns below
			
date		time	Notes
19990208	0021	Ship moving slowly
19990208	0202	nd
19990208	0330	nd
19990208	0414	nd
19990208	0500	Ship moving slowly
19990208	0530	nd
19990208	0907	nd
19990208	0955	nd
19990208	1000	nd
19990209	1235	Below LOD
19990209	1243	Below LOD
19990209	1308	nd			
			
Mean		0.08		
Std. Dev.	0.03		
n		10		
2 		rejections		


Acquisition description

See SOIREE Preliminary Voyage Report

Underway Fe Mapping
(Andrew R. Bowie, UoP / PML, UK)

Objectives
(i)To map the ambient concentration and investigate surface water changes in Fe2+,
dissolved (diss-Fe, <0.2mm) and total dissolvable (TD-Fe) iron during the experiment

(ii)To study the vertical distribution of Fe INside and OUTside the fertilised 16
patch via laboratory based analysis of sub-samples taken from daily Go-Flo casts

(iii)To perform an intercalibration exercise between FI-CL (AB) and solvent extraction
GFAAS (RF) technologies from identical samples taken from Go-Flo casts

(iv)To study the surface water distribution of Fe and other trace metals along a latitudinal
transect of the west coast of New Zealand

Analytical and Sampling Methodologies
Shipboard determinations were performed using a semi-automated flow injection chemiluminescence
(FI-CL) analyser. The technique enabled real-time analysis of Fe2+, diss-Fe and TD-Fe fractions
at the sub-nanomolar concentration level. The system is based on the oxidation of luminol, which
is catalysed by Fe2+ ions, emitting blue light. A reduction step was performed to determine the
Fe(II+III) fraction and in-line matrix elimination / sample preconcentration was achieved using
a 8-hydroxyquinoline micro-column. Surface samples were taken from a torpedo-style fish deployed
at 1-2 m and pumped directly into container designed for trace metal work. Vertical profiling
samples were collected from 5L and 30L trace metal Go-Flo sampling bottles deployed on Kevlar rope.

Preliminary Results
The FI-CL system performed with only minor problems throughout the one-month cruise period.
A minimum of 50 samples were analysed during each mapping period for Fe2+, diss-Fe and / or
TD-Fe fractions. Ambient surface water diss-Fe levels (0.08 nM) were raised to ca. 2 nM on
the first infusion, to 1 nM during infusions 2 and 3 and to 2nM on infusion 4. Rapid loss of
diss-Fe INside the patch to near ambient levels was noted after the first 3 infusions; this
was due to the conversion of the added iron sulphate heptahydrate to colloidal and particulate
phases. However, >1 nM diss-Fe persisted INside the patch for the 5 days following the 4th
infusion. Furthermore, significant concentrations of Fe2+ species existed INside the patch on
days 12 and 13 of the experiment. Maximum surface water TD-Fe levels (>5 nM) were measured on
day 8, following the 4th infusion.

Processing description

See SOIREE Preliminary Voyage Report

Underway Fe Mapping
(Andrew R. Bowie, UoP / PML, UK)

Objectives
(i)To map the ambient concentration and investigate surface water changes in Fe2+,
dissolved (diss-Fe, <0.2mm) and total dissolvable (TD-Fe) iron during the experiment

(ii)To study the vertical distribution of Fe INside and OUTside the fertilised 16
patch via laboratory based analysis of sub-samples taken from daily Go-Flo casts

(iii)To perform an intercalibration exercise between FI-CL (AB) and solvent extraction
GFAAS (RF) technologies from identical samples taken from Go-Flo casts

(iv)To study the surface water distribution of Fe and other trace metals along a latitudinal
transect of the west coast of New Zealand

Analytical and Sampling Methodologies
Shipboard determinations were performed using a semi-automated flow injection chemiluminescence
(FI-CL) analyser. The technique enabled real-time analysis of Fe2+, diss-Fe and TD-Fe fractions
at the sub-nanomolar concentration level. The system is based on the oxidation of luminol, which
is catalysed by Fe2+ ions, emitting blue light. A reduction step was performed to determine the
Fe(II+III) fraction and in-line matrix elimination / sample preconcentration was achieved using
a 8-hydroxyquinoline micro-column. Surface samples were taken from a torpedo-style fish deployed
at 1-2 m and pumped directly into container designed for trace metal work. Vertical profiling
samples were collected from 5L and 30L trace metal Go-Flo sampling bottles deployed on Kevlar rope.

Preliminary Results
The FI-CL system performed with only minor problems throughout the one-month cruise period.
A minimum of 50 samples were analysed during each mapping period for Fe2+, diss-Fe and / or
TD-Fe fractions. Ambient surface water diss-Fe levels (0.08 nM) were raised to ca. 2 nM on
the first infusion, to 1 nM during infusions 2 and 3 and to 2nM on infusion 4. Rapid loss of
diss-Fe INside the patch to near ambient levels was noted after the first 3 infusions; this
was due to the conversion of the added iron sulphate heptahydrate to colloidal and particulate
phases. However, >1 nM diss-Fe persisted INside the patch for the 5 days following the 4th
infusion. Furthermore, significant concentrations of Fe2+ species existed INside the patch on
days 12 and 13 of the experiment. Maximum surface water TD-Fe levels (>5 nM) were measured on
day 8, following the 4th infusion.

BCO-DMO Processing Notes
Generated from original file SurfaceFe.xls, Tabs: Notes, Pre_release, and map1-map13
provided on the Deep-Sea Research II 48 (2001) accompanying CD-Rom

BCO-DMO Edits
- parameter names modified to conform to BCO-DMO convention
- individual SOIREE Map, Yr, SDAY, etc record commented and added as columns to each data record
- added negative sign to latitude values
- 2 original column header records re-organized into one header line
- No data or Bad data flag changed to BCO-DMO standard of “nd"


Field Names List

ParameterDescriptionUnits
datedateYYYYMMDD
timetimeHHMM
UncorrPosEEastward position of shiptrack kilometers
UncorrPosNNorthward position of shiptrack kilometers
DriftEEastward drift calculated from ADCP kilometers
DriftNNorthward drift calculated from ADCP kilometers
CorrPosECorrected ship-track (Eastward component) kilometers
CorrPosNCorrected ship track (Northward component) kilometers
lonlongitude, negative denotes Westdecimal degrees
latlatitude, negative denotes Southdecimal degrees
DfeDissolved IronnM
YearYear of dataYYYY
MapMap number of mapping sessioninteger
SDYDay of the yeartext
SOIREEDayDay of SOIREE Experiment (Day 1=10Feb1999)integer
DayDateDay/Date of DataDD-Mon
TimeDecimalDays in February 1999 (GMT) with 1 February 1999 0:00 = 1.0000decimal days
YrYear of dataYY

Platforms List

R/V Tangaroa 61TG_3052

Instruments List

  1. Undulator:

    On SOIREE, the undulator did not undulate.
    As a result, it was towed at a constant depth of 1-2 meters


This document is created from the content of the BCO-DMO metadata database.    2010-03-18  00:56:35

info app: /home/bco/dbase-v2 v.100108 CLC
Data URL: http://data.bco-dmo.org/jg/serv/BCO/Fe_Synthesis/SOIREE/61TG_3052/SurfaceFe.