BigJohnny
Active member
Please read the TTM sticky for the answers to all of your questions. It makes no sense to reiterate here.
Thanks, I'm not aware of everything that currently exists on this forum so I appreciate the link.
Please read the TTM sticky for the answers to all of your questions. It makes no sense to reiterate here.
Haha ok well then how long does it take if you do one transfer each week with CP? also what is HT?
That is clearly true. TTM can be messed up but the variables are more controllable. Hyposalinity as a treatment depends on factors such as the standard error of the mean in the refractometer being used as well as auto top off methods to control salinity.
So wait, you don't even use CP?Yes, there are measurement insecurities like with everything else (i.e. copper tests). I don't agree that the refractometer errors are significant enough to mess up the treatment. The effective salinity range is larger than usually claimed here. Anything between 1.011 and 1.009 will work. And that isn't a small range.
Of course a refractometer that is to be used for hyposalinity treatment must be calibrated with distilled or RO water and not with a 35 ppt standard solution
(I never really trust those solutions fully anyway as a little evaporation can spoil it). You want it to be accurate at the low end of the scale.
As for evaporation - at the low salinities required for hyposalinity the effect of evaporation is significantly less than at regular reef tank salinities. I found manual top off in the morning and evening sufficient. A tank cover to limit evaporation would make it even more stable (and should be in place to protect the fish form jumping anyway).
The only argument against hyposalinity that holds water are the Taiwanese low salinity strains. But I don't think it's very likely that those made it here. And if you got them or done something wrong you will know after about a week of treatment.
Also I would only use hyposalinity as a treatment of visibly infected fish, never as prophylactic measure. For the latter TTM is the method of choice.
I use CP when I suspect velvet or uronema on new fish.
I never had the chance to use it against an ich outbreak, but others used it with great success. The issues with it are that long term exposure may cause "unexplained" deaths of fish. That's why I would only use it in a QT/HT and only for 2 to 3 weeks. After those 2 or 3 weeks the fish need to be transferred to an ich free tank for further observation.
CP can not be used on any member of the Syngnathidae family (seahorses, pipefish and their relatives). There are also some wrasses that won't tolerate it. With these you are better off using TTM.
Hyposalinity works well but may require an extra week for raising the salinity. So I would only use it with a full outbreak and too many fish to handle through TTM.
Endless discussion is a good thing brotha, that's what we're here for! Thanks for your input!wow this is an endless discussion as stated above many methods work. and each have drawbacks.
TTM WORKS FINE IF ITS ONLY CRYPTO BUT IF OODINIUM IS IN THE MIX YOUR IN TROUBLE.I have always used hypo for 2 weeks @ 1.012 and chelated copper. Copper power to be exact and it is relatively non toxic and stays effective for 1 month.after two weeks i gradually allow salinity to increase by not topping off.When the qt is equal to the display tank salinity I remove the copper via carbon and keep the fish in qt for at least 90 days. ick is eradicated from the qt because the copper kills the free swimming form and the embedded forms have all dropped off or crushed during the hypo. this method also kills oodinium and if you suspect brook go down to 1.010 but not more than 2 weeks or you will cause irreversible kidney damage.I certain that some will disagree with me but its safe and most of all it works. the QT temp is at 85F during the first 2 weeks and heavily aerated.with a course bubble glass air stone A seasoned sponge filter which was aged in the display tank sump WORKS FINE AND IS UNAFFECTED by copper power.