My pond culture has reached its 100th day and I seem to have hit upon a wonderful ecological equilibrium. Yet, there is a certain impatience to see more, which is why I thought I’d make a hay infusion. The hay infusion is a wonderful concept. Making it is rather trivial (see Figure 1): Cut some hay (I use Timothy hay available at a pet store) into 1-3 inch pieces, boil it in water for 10 minutes and you have a hay infusion. I used bottled water but would recommend the same pond water; tap water might also be fine. I made up the lost volume (due to boiling) with more water and let it cool. I then took about 5 ml of the pond water, avoiding the duckweed and invertebrates in the pond water (as much as I could see) and inoculated the hay infusion.
The idea is to inoculate a hay infusion with pond water. First the fast growing bacteria will try to win the race by consuming the rich medium. Once the bacteria reach a sufficient density, predators of the bacteria, if present, will grow in numbers, and there their predators will grow and what you get is a grand symphony of successions. It is a wonderful way to teach ecological concepts such as R- and K-selection . It is also a great way to enrich ciliates.
Post-inoculation, I actually forgot about it in the hustle and bustle of daily life. Last night, which was the 8th day post inoculation, I saw a biofilm on the surface (Figure 2) and decided to investigate it by making a slide with bits of the biofilm itself.
At 430x magnification, the tiny bacteria can now be seen, although just barely, but the other cells comes into view a bit more clearly. They seem to be a eukaryotic flagellate and they have a depression like the flagellate that showed synchronous disaggregation . I suspect they are the same type. I will be on the lookout for a repeat show of synchronous disaggregation, but I think I am already seeing the symptoms in these.
I am planning to play with this culture a bit more. Have a ton of experiments to try out. Look out for more on this. For those interested in culturing ciliates and bacteria in a home lab setting, I would high recommend Richard Howey’s article on the same. Click here to access it.