This close minded dogmatism is exactly why we have been without answers about RTN and STN for 50 years.
1. I used a microscope for all experiments. You can see bacteria with a microscope, that’s how they were first discovered. There were no funguses nor viruses nor bacteria, only protozoans and their bellies were full of coral tissue and zooxanthella. No other microorganism was present. I used a microscope and micro pipette to isolate Philaster
2. Protozoans are not worms
3. Extensive testing was performed on treated systems and there were no effects on anything in the reef system except the protozoans and if overdosed fish will die. The in tank treatment affects fishes ability to have gas exchange across their gills, that is the reason.
Thanks - this explains part of it. BTW I think its fascinating work - so dont take my comments as insulting.
1. IMO Using a microscope is not enough. Especially not the microscope you were using at least in some of the videos. Yes - you can 'see bacteria' under a microscope when they are in a solution - you cannot see bacteria attached to a hard piece of coral (unless perhaps its an electron microscope).
2. Obviously protozoans are not worms - but I believe I read in the product literature that this product also affects flatworms, etc - are we sure it doesnt affect others as well?
3. So you're contradicting the statement from your webpage that: Prime Coral Stop RTN is a complete coral dip used to treat common coral parasites. It is the only treatment effective against RTN, STN, and Coral Bleaching parasites; acropora eating flatworms, montipora eating nudibranchs, polyclad worms, black bugs, common flatworms, and eggs. PS I know the products are 'different' - I just didnt know they were 'that different'. PPS - since ciliates can also be brought in on CUC - are they also safe to dip?
Can you answer these questions?
1. How are you sure that you have a 'pure culture' of Philaster lucinda? How was that documented? DNA analysis or visually (which would seem to be quite hard)
2. Much of the research (published) suggests that at best the ciliates are a secondary infection - feeding on damaged coral and that when THEY looked at samples using tissue sections bacteria of many types was always present - what's your response?
3. When you did your experiment where you exposed the coral to Philaster (the healthy coral) - how did you determine the concentration of Philaster you added to each container. I mean in enough numbers almost anything will be killed but that doesnt mean those concentrations would ever be present in the wild or in a tank.
4. Since you had sources of coral free of Philaster (how did you determine that - DNA analysis of samples, etc). Did you ever try to induce RTN with rapid changes in tank parameters (alkalinity, temp, etc). The problem I see with one part of the logic is that if these things didn't play a role in RTN, why do so many people describe problems with RTN after such an event?