|
|
Sample |
Filter |
Vol |
Container |
|
Amt |
Storage |
Notes |
|
1 |
Chl |
GFF |
280ml |
scint.vials |
acetone |
10mls |
freezer |
Keep
in dark |
|
2 |
Chl frac. 1m |
1m nuclepore |
100ml |
scint.vials |
acetone |
10msl |
freezer |
Keep
in dark |
|
3 |
Chl frac. 5m |
5m nuclepore |
100ml |
scint.vials |
acetone |
10msl |
freezer |
Keep
in dark |
|
4 |
T0 0.1% |
GFF |
280ml |
scint.vials |
none |
n/a |
freezer |
Treat
w/C14 |
|
5 |
T0 100% |
GFF |
280ml |
scint.vials |
none |
n/a |
freezer |
Treat
w/C14 |
|
6 |
POM |
CombustedGFF |
4L |
petri dish |
none |
n/a |
freezer |
Use
the big filters |
|
7 |
POC |
CombustedGFF |
500ml |
glassine |
none |
n/a |
freezer |
|
|
8 |
A* |
GFF |
1L |
cryovial |
none |
n/a |
nitrogen |
Nitrogen
in Thermos |
1. Chlorophyll
: 11 depths, 0m 5m 10m 20m 30m 40m 60m 80m 100m 150m 200m
2. Chlorophyll
1m
Fractionations : 1 depth, 0m
3. Chlorophyll
5m
Fractionations: 1 depth, 0m
4. T0
0.1%: 1 depth, Light Penetration Depth = 0.1% as determined by Secchi Index
5. T0
100%: 1 depth, 0m (Note T0=Time Zero,
treated with C14 and processed ASAP)
6. C14
at light penetration depths (re:Secchi),
100%,50%,30%,15%,5%,1%, and 0.1%. Water
samples are incubated first then filtered.
Store bottles in corresponding light level incubator sleeves.
7. POM:
1 depth, 0m from Underway Mapping System (POM=Particulate Organic Matter). Note temperature, GMT, Volume Filtered on
NASA Data Sheet in Cruise Notebook.
8. POC:
1 depth, 0m. POC=Particulate Organic
Carbon. Use combusted GFF filter, fold filter and store in Glassine envelope, record volume
filtered on envelope.
9. A*:
4 depths, 0m 10m 20m 40m. Store in cryovial, then in Nitrogen . At Mooring1 only.
10. Nutrients
: 11 depths, 0m 5m 10m 20m 30m 40m 60m 80m 100m 150m 200m at Mooring1 only, 0m
depths at C1 and Mooring2. Nutrients are
not filtered. Store vials in freezer.
Note: Any deviation from the above
procedures should be noted on the Data Sheet.
i.e. Volume Filtered is more/less than
required, or filter dropped on table, etc.