Does extra CO2 improve phytoplankton growth in culture?

F-28 was aerated using a pasteur pipette attached with rubber tubing and airline hose to an aquarium pump. The volumes needed for measurements and dilutions were removed and added using a sterile pipette. F-27 was not aerated.

In order to take measurements and dilute the appropriate volume was pipetted in and out of the flask. F-26 was not aerated either. In order to obtain culture for measurements and dilutions the appropriate volume was poured into and out of the flask.

No pipettes were used. All flasks were shaken to suspend cells evenly before fluorescence measurements were taken. These flasks had to be diluted often both before and after these trials began.

As a result, obtaining three points for calculating a growth rate was difficult. We calculated three different growth rates for each flask and took averages. Later, upon comparing the length of the cells in the same culture of the previous year, we noticed that the cells were significantly longer this year.

This told us that the increased growth, health, and chain length was due to the culture undergoing sexual reproduction. The data we have shows that the aerated culture had the best average growth rate followed by the pipetted culture and finally the pour culture.