Sproul Cruise September 22 - 23, 2007
Multicorer Instructions
MULTICORER DEPLOYMENT/RECOVERY TEAM:
1) Record the date, station number, latitude, longitude, bottom depth, time of deployment and
time of recovery on the data sheet.
2) Carefully measure the length of sediment recovered for each core and enter this information
on the data sheet.
3) Examine the sediment surface and overlying water in each core. Describe any macrofauna,
mounds, tracks, trails, detritus, etc. and write the descriptions on the data sheet.
4) Examine each of the cores. Make a diagram of the core indicating any layering, color
changes, textural changes, organisms, burrows, or other features observed. Be sure to note
the depth (from the top of the core) of each feature.
5) Subsample each of the cores according to the protocols established for each course.
MULTICORER SUBSAMPLING
I. Bottom water samples for MARS 452/512
a) For two cores per station, siphon off the water just above the sediment/water interface into a
250 ml Nalgene bottle.
b) Fill in leg number, station number, Niskin bottle number, water depth.
c) Place all MARS 452/512 water bottles in chest freezer.
II. Sectioned cores for BIOL 451W/MARS 511
a) Using a handheld meter, measure the temperature, salinity and dissolved oxygen
concentration of the water just above the sediment in each core.
b) Siphon off the liquid just above the sediment/water interface.
c) Extrude and slice core sections over the following intervals:
1. 0-3 cm
2. 3-10 cm
d) Sieve each sediment sample through nested 1 mm and 500 µm stainless steel sieves using
seawater. Rinse the samples gently, trying not to blast organisms through the screens with a
powerful stream of water.
e) Carefully transfer organisms from the screens into sample containers for preservation. Each
container should be labeled with the station number, time, date, water depth, core number,
and section information (0-3 or 3-10 cm). Also include an internal paper label with the
same information, in case something happens to the exterior label.
f) Add MgSO4 solution to fill approximately 85% of the volume of the container. This
solution will “relax” the animals and make them easier to examine after they’ve been
preserved.
g) At least 15 minutes later, add enough buffered 37% formaldehyde solution to fill the
container to 95% of its capacity. This solution will preserve the organisms for study.
