The other group was doing CTD casts off the side and filing 7 Niskin bottles separately. I filled up 2 x 20L carboys at each station and brought them back to the lab at Palmer. I set up a 57 bottle incubation using various radioactive organic carbon compounds, for example radioactive glucose and amino acids, etc. Most of my incubations were 4 hours long but one went as long as 8 hrs. After incubations comes filtering the water onto thin filters for either microscopy later on back in DE or scintillation counting which we did immediately. I didn't leave the lab till about 10pm, but it was a good day.
Yesterday I spent filtering more and babysiting the stupid scintillation counter- it didn't like my bottles and I had to insert each one manually- which took from 6:30pm to about 11:30pm, joy. Today I finally got to analyze some data and take it easy. Results look good so far- the bacteria are using the compounds I added to the water. The two stations look a little bit different but not a huge difference, which is good since they are only 2 miles apart, shouldn't be a big difference.
We are planning to sample again tomorrow- although the weather looks like there might be a storm brewing with 25-40 knot winds. We may end up stuck inside. We've been lucky to have beautiful weather thus far though, so I guess that makes up for it.
You never did say: did you have to jump in the waters? :)
ReplyDeleteThat is something station people do when the boat leaves to go back north, which it won't do until February (in which case I will be on the boat). Currently it's gone southward to do more sampling. Not that I would jump in the water anyway, I am sensitive to the cold.
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