US JGOFS Antarctic Environments Southern Ocean Process Study (AESOPS)

Revelle Leg KIWI08, APFZ Survey 2,  8 Jan. - 8 Feb.  1998

Documentation for:  The Trace Metal Rosette Hydrographic bottle data

L.A. Codispoti (lou@ccpo.odu.edu)
Old Dominion University,  December, 1998

General Comments:

This "readme" file pertains to the salinity, dissolved oxygen,
and nutrient data taken from sampling bottles with the trace
metal rosette that was equipped with 8 ~30-liter  teflon coated
"Go-Flo"  bottles made mostly of PVC and equipped with orange
silicone o-rings during Revelle leg RR08 (8 January - 8 February
1998).  This rosette system was equipped with a Sea-Bird  SBE-19
CTD.  Dr. Kenneth H. Coale of the MossLanding Marine Laboratories 
(coale@mlml.calstate.edu) was the chief scientist during this
leg.  This cruise was the second survey leg on the R/V Roger
Revelle during the U.S. JGOFS program in the Southern Ocean
(AESOPS).  The Revelle legs focused on the Polar Front region and
complemented several AESOPS cruises on board the R/V Nathaniel
Palmer that focused on the Ross Sea.  Several casts with a
hydrographic rosette equipped with 24, 10-l Bullister  bottles
and a higher resolution CTD system were also taken during this
leg. These hydrographic data are of "WOCE" quality and have been
submitted as a separate file because of the different
capabilities of the two CTD/rosette systems.  Additional
hydrographic data were collected by other research teams, and
will be submitted to the data base by these groups.  These
additional observations included observations from towed
undulating devices  and from trace metal clean bottle casts made
by hanging bottles on Kevlar cable. Investigators interested in
these data can find out about their status by consulting the
chief scientist. The user should also be aware that considerable
underway hydrographic data were also collected during this leg
and these data are not included in this report.  

Some questionable data are not included in this report. These
data are available upon request.

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IN PARTICULAR, PLEASE NOTE THAT PROBLEMS WERE ENCOUNTERED WITH
THE AMMONIUM ANALYSIS AT THE BEGINNING OF THIS CRUISE.  THUS, 
AMMONIUM DATA ARE NOT REPORTED UNTIL STATION 4, CAST 2 IN THIS
REPORT AND UNTIL STATION 4, CAST 3 IN THE COMPANION HYDROGRAPHIC
ROSETTE DATA REPORT THAT HAS BEEN SUBMITTED TO THE JGOFS DATA
BASE.
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No units are given for salinity in this report because the most
recent definitions of salinity define it as a dimensionless
number.  To accommodate every preference, Winkler oxygen values
are reported in ml/l, micromolar and micromoles per kg.  The
latter values can only be calculated with a knowledge  of the
oxygen sample temperatures when the samples were drawn.  These
"draw temperatures" are not reported here, but can be obtained by
contacting lou@ccpo.odu.edu.  Nutrient values are reported in
micromolar.  For the laboratory conditions on this leg, the
nutrient values in micromolar can be converted  to micromoles per
kg,  by combining a temperature of 21 deg. C and the  salinity of
the sample to compute density and then dividing the value in
micromolar by this number.

Methods:

In general, the methods employed for the bottle salinity, Winkler
dissolved oxygen, and nutrient analyses did not differ
significantly from those described in the JGOFS protocols that
were distributed in 1994 (UNESCO, IOC Manual and Guide #29). 
Minor differences included the following:  1) The protocols give
one a choice of adjusting nutrient methods so that  calibration
curves are strictly linear, or opting for more response and
taking into account non-linearities.  We choose the latter
method.  2) No corrections were made for "carryover" between
nutrient samples run on the Technicon Autoanalyzer. Carryover
effects in our nutrient analyses are generally less than ~2% of
the concentration difference between adjacent samples, and were
minimized by arranging samples in depth order, etc. in some
cases.  3) Calibration and re-calibration of volumetric ware were
not exactly as described in the JGOFS protocols, but all
volumetric flasks, maxipettors, and dosimats were  calibrated. 
4) Duplicate oxygen samples were not routinely drawn.  5) The
JGOFS protocols do not describe an automated technique for the
analysis of ammonium concentrations.  We employed the Berthelot
reaction  using a method somewhat similar to the method described
by Whitledge et al. (1981, Whitledge, T.E., Malloy, S.C., Patton,
C.J. and Wirick, C.D. Automated Nutrient Analyses in Seawater.
Brookhaven National Laboratory Rept.  BNL 51398, 216pp.). 

Temperature:

The temperature data associated with each bottle depth were taken
by the CTD system during the bottle tripping process.  Consult
the companion CTD data report for this cruise to learn more about
the CTD system.     

Sampling:

The samples in this report were taken from ~30 liter Go-Flo
bottles.  Because there is little or no lag time between
triggering a bottle and bottle  closure with the new Sea-Bird
rosette systems, our sampling protocols request  that bottles be
held at the sampling depth for at least 30 seconds before 
tripping.

NOTE THAT THE MID-POINTS OF THE SAMPLING BOTTLES WERE ~ O.5 METER
ABOVE THE CTD SENSORS.  THE DATA HAVE NOT BEEN CORRECTED FOR THIS
OFFSET. 

Salinity:

Salinities were determined with Guildline Autosal salinometers. 
New vials of  standard sea-water were used to standardize before
and at the end of every run.  Agreement between bottle salinities
and the recently calibrated sensors  on the Sea-Bird SBE-19 CTD 
was usually better than 0.02 before post-cruise data processing
which employs the bottle salinities to correct the CTD
salinities.  Some larger differences occurred in gradients
because of the response time characteristics of the sensors in
this system which did not produce high quality data in gradients
during the cruise. More information on the quality of thesalinity
data are given in the companion CTD report. 

Dissolved oxygen:

The Winkler dissolved oxygen apparatus was built and supplied by
the Scripps Institution of Oceanography's (SIO) Ocean Data
Facility (ODF) group.  This system is computer controlled and
detects the end-point photometrically.  Temperatures of the
thiosulfate and standard solutions are automatically  monitored
by this system.  

Nutrients:

Note that the terminology used to describe nutrients has become
somewhat loose over the years and that silicate = silicic acid,
dissolved silicon or reactive silicate, and phosphate = reactive
phosphorus.  Nutrient analyses were performed on a 5-channel
Technicon II AA system that was modified and provided by Doug
Masten (doug@odf.ucsd.edu) of  the ODF group at the Scripps
Institution of Oceanography.  ALSO READ THE NOTE REGARDING
PROBLEMS WITH THE INITIAL AMMONIUM RESULTS IN THE "GENERAL
COMMENTS" SECTION ABOVE.

Queries:

Questions about these data may be addressed to:

Dr. L. A. Codispoti
CCPO
Old Dominion University
Norfolk, VA 23529
lou@ccpo.odu.edu