Today on another thread Jim Welsh wrote:
"Studies have shown that excessive density of adult copepods can have an adverse effect on nauplii production, e.g., "Management of nauplius production in the paracalanid, Bestiolina similis (Crustacea: Copepoda): Effects of stocking densities and culture dilution", VanderLugt and Lenz, 2008. In short, assuming that you succeed in producing a large number of copepods in your culture, and a large number of them survive to adulthood, it is very likely that the increased density will result in a significant decrease in egg production, and possibly cause a sudden crash of the copepod culture, once the adult population dies off due to the limited natural lifespan. In other words, if you are successful at culturing these copepods, it is important to regularly split, harvest, dilute or otherwise manage the adult density in order to sustain a relatively high nauplii production rate. More on this to follow."
Does this follow for rotifers? Could this be the reason that my newly split cultures aren't getting thicker. I know I have live rotifers, I can see them under the scope. But for the last 3 days the cultures aren't getting less green. Even the one contaminated with brine shrimp. I can't figure what I should do to get back on track.
When I split them, they were going clear regularly and I had no fry in need of feeding. Anticipating a hatch, I sieved the cultures before I tossed the waste. Now the cultures don't loose their green. I have both RGComplete and live phyto.
What is the tried and proven method to create a new dense culture from a sick one.
How do I tell a) if there are enough nauplii in the start sample b) how large a sample should I start with and c) what ratio of starter to SW to RGComplete.
Because obviously I'm not getting it.