contact PIs:Data Object primary_production
| name | title |
|---|---|
| Dr Richard Barber | Principal Investigator |
| Dr Walker O. Smith | Co-Principal Investigator |
dates: 24 January 2002 to 20 February 2002 (20020124-20020220) location: N: -52.385 S: -66.612 W: -172.693 E: -166.939 project/cruise: SOFeX/MV
12 February 2008: Prepared for OCB data system by Dave DuBois (WHOI) Cyndy Chandler, OCB DMO (WHOI) from documentation contributed by originating PI, data analysts and technicians.
Original Excel file downloaded from MBARI: copy of original Excel file
Contact: Anna Hilting (Duke University Marine Laboratory)
R/V Melville Extracted Chlorophyll Methodology
Please direct questions to Sara Tanner (tanner@mlml.calstate.edu) or Jodi Brewster (jbrewster@mlml.calstate.edu)
Water samples were collected from 12 depths on the CTD Rosette and 8
depths on the TM Rosette. The TM Rosette depths were chosen at the 100,
45, 30, 16, 10, 5, 1, and 0.1 percent light levels (so phytoplankton
production can be related to phytoplankton biomass) (Evans et al 1987).
The CTD also had 2 more depths scattered between .1 and 100 percent and
one each at 200m and 300m. The water from the CTD and TM rosettes was
collected using opaque brown bottles in 250, 500, 1000, and 2000 ml or
white 100 ml bottles. The differing volumes depended upon the depth of
the sample and whether the samples were taken within the patch or not.
Sampling from the TM Rosette was done with gloves. Each bottle was
rinsed three times with the sample water before filling to the neck of
the bottle.
A Whatman G/FF glass Fiber Filter, (~0.7um) Polycarbonate 5 um filter, or
Polycarbonate 20 micron filter was placed in a 25 mm diameter Gelman filter
holder. Water was pumped through the filter, being careful the vacuum
pressure did not get above 6 psi to avoid cell lyse. After filtration, the
vacuum was turned off and the filter was added with forceps to a tube
filled with 8 ml of 90% acetone. The tube was labeled and stored in a
freezer for a minimum of 24 hours.
After the minimum 24 hours extraction time, the filter was removed from
the tube and the tube was wiped down with Chem Wipes. The fluorescence of
the chlorophyll extracts were read on a 10AU Turner Designs fluorometer.
Two drops of 10 % HCl was added and the fluorescence was reread and
recorded again. The "before" and "after" readings were plugged into
equation chl-a = K * (Rb-Ra) * (vol ext/vol filtered)*dil to calculate
chlorophyll a values.
A standard made from Sigma Chl-a in 90% acetone was calibrated on a
spectrophotometer and used to calibrate the fluorometer at the beginning,
mid and end of the cruise. Due to the fact the fluorometer drifted both ±
according to the solid standard, and a high correlation was found between
the low solid standard and the calibration curve, Chlorophyll-a values were
corrected using the ratio of the low solid standard.
Change history: YYMMDD
061228: downloaded original data (MelvilleProductivity.xls)
from SOFeX project data web site
080212: added to OCB database by Dave DuBois (WHOI) and Cyndy
Chandler, OCB DMO, (cchandler@whoi.edu)
OCB DMO Processing Notes
Data file records were sorted by event_SFX. underway Survey measurements were added sequentially into Day 45.
For underway Survey data, Station value 'u/w' was replaced with 'SCUFA' (Self-Contained Underwater Fluorescence
Apparatus). Cast was also renamed to ev_type and 'u/w' was replaced with respective 'S 159', 'S 160', etc... values. event_SFX matches those found in Michael Hiscock's multi-ship event log.
Note that the Year Day and patch day values do not agree with Hiscock's event log, nor do most of
the 'Landry' Cast Types.
SCUFA or Self-Contained Underwater Fluorescence Apparatus
SCUFA brochure from Turner Designs
PI Notes
from Richard Barber (rbarber@duke.edu) and Anna Hilting (ahilting@duke.edu)
These data have been edited for quality control but will be processed further for
size-fraction analysis and integration using the Morel Model. See Barber et al., 1997 and
Hiscock et al., 2002. Incubated depth will be calculated using the Morel model and added later.
Original Excel file
of SCUFA chlorophyll calibration work for underway surface extracted chlorophyll
Plots of chlorophyll and primary productivity for Revelle and Melville (PDF file created from MS Word .doc original format from Barber and Hilting)
| Parameter | Description | Units |
|---|---|---|
| patch_id | sampling patch (North or South) | dimensionless |
| patch_loc | sampling location relative to patch | dimensionless |
| station | station identifier | dimensionless |
| ev_type | event type description | dimensionless |
| cast_type | type of cast | dimensionless |
| event_SFX | SOFeX sampling event number; composite of date and time (UTC) | YYYYdoYhhmm |
| lat | latitude, negative denotes South | decimal degrees |
| lon | longitude, negative denotes West | decimal degrees |
| yrday | date sampling began (GMT) | dd.ddd |
| pDay_N | North patch days since midpoint of first fertilizaton; day 0 = 012/02 | decimal days |
| pDay_S | South patch days since midpoint of first fertilizaton; day 0 = 024/02 | decimal days |
| Nis | Niskin bottle number | dimensionless |
| depth_n | intended nominal sample depth | integer meters |
| depth | actual sample depth | decimal meters |
| irrad_surf | percent Surface Spectral Irradiance (E0%) | integer percent |
| chl_a_GFF | Glass Fiber Filter chlorophyll a | milligrams Chl/meter^3 |
| PrimProd_GFF | Glass Fiber Filter Primary Productivity | millimole C/meter^3/day |
| phytoBiom_GFF | Glass Fiber Filter Phytoplankton Biomass | millimole C/milligram Chl/day |
| R/V Melville COOK19MV | R/V Roger Revelle DRFT08RR |
This document is created from the content of the BCO-DMO metadata database. 2009-11-22 10:03:37
info app: /home/ocb/dbase v.090827 CLC