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This is what I was referring to when I said some bacteria helps suppress dinos, and some helps fuel it. And we have yet to see a reliable way to know what bacterial source is sure to give you "good" bacteria.I had Ostreopsis and they loved it when I dosed MB7. Bloom went from bad to worse fast.
I didn't mean anything other than what you referred to when you addressed the gloves and poking around in the tank.I thought about this statement more and I'm curious if you could be more specific?
I can't prove or even elucidate the connection, but I see dinos and cyano associate together too much to be comfortable with persistent or recurring cyano in a tank that's had a history of dinos.
That said, popular treatments for killing cyano (chemiclean etc) seem even more strongly associated with dinos than cyano itself is!
For those who have dinos that don't move into water and aren't reachable by UV (Large cell amphidinium), silica fueled diatom competition may be a helpful tool.I've not looked, but have people been successful with diatoms driven by silicate dosing to outcompete dinos?
It's speculative (worked for an aquaculture facility, and maybe in a couple of tanks?) and may be a dead end, so those interested I recommend follow along on this other thread.
For every other kind of dinos, there are enough mechanisms to control them that I can't see the point in suggesting Silica (yet).
Your report is interesting because even with high quality Coralife UV, some have not had success at this wattage per gallon. I'm guessing ostreopsis dinos? They seem the most UV susceptible.You could always take the route that I went with the coralife 6x, its 18w but it decimated Dinos in my 90 gal, didn't even put it in the display, right off my return manifold and in a day or two it was all gone. Again I did a few things prior such as raising my N and P and keeping it high, changing my socks everyday after blowing it off all the time. Removing GFO, and I stopped doing any water changes. I also lowered my light schedule by an hour or two.
Also I bolded the extra things you did that are not usually headlines in this thread, but important ways to increase the effectiveness of a nutrient + UV approach.
This looks very likely to be dinos, and stringiness suggests probably susceptible to UV.Is that this is can get rid of
FYI, shaking chaeto vigorously in freshwater will destroy Ostreopsis cells in seconds. live and cysts too.Fresh water isn't 100% versus all dinos (prorocentrum survives somehow), but it is 100% vs ostreopsis.Being overly optimistic I decided to throw some cheato back in the sump and fire up the lights. Bad move. Within one week, the o. dino’s erupted in the sump and I had to throw away the cheato, vacuum out the sump, and leave the lights off (in the sump). The UV remains in the DT and the dino’s are staying out of there.
I've cultured up dinos in beakers and super nano tanks. nothing made them bloom harder than amino acids.3. I then realized I could not detect any PO4/NO3. 5x my feeding, dosed aminos, dropped a ridiculous amount of frozen cubes of mysis in, still nothing. Dinos exploded in growth (I guess all the NO3/PO4 was feeding dinos).
Yep, hence the other thread I started for Amphidinium and Silica experimentation. I'd hate people to get confused between this Si stuff only tried in a couple of tanks, and the main thread points that have been tried by many.It's hard to say "what went wrong" since it was so much theory and hope....it's very possible it just doesn't work, or doesn't work like we think.
It was worth a shot, regardless! And if you have the capacity to keep testing, maybe you'll still figure something out.
Good questions, and frustration is understandable. However let me ask this.... but besides doing all that any other disturbances could cause a rebloom? Where does it stop?
how do the numbers compare to the original bloom? significantly less?
If so, what's to say this is not the minority of cells that encysted at the end of the last bloom and are re-emerging in greatly reduced numbers. After all - you let them just "burn themselves out" last time and that sort of condition is likely to trigger encystment like at the end of a growing season.
I get that it looks and feels like a step backwards, but I don't see any reason to jump to that conclusion.
I don't begrudge anyone their success, but since it's 180degrees opposite from what most experience, it's hard to generalize or recommend this.My theory was that the NoPox addition is taking nutrients out before the dinos can consume them. Less food + DinoX seems to have worked for me.
This may be very specific to how my system runs (not really sure what makes it do that)
As I said in the other thread, it looks to me like this is ~10:1 diatoms to dinos. So if you had more grazers to match the diatom growth, your sand would be 90% less brown. Maybe this is still an unacceptably large amount of brown, but maybe some of those grazers would munch a few dinos too.I’m at a loss as to why the Dino’s keep coming back. I thought my higher levels would not bring on there return. It’s not the thick snotty mess that I had but I can see the difference in color, golden brown for diatoms then darker brown in the Dino concentrated areas. If I keep the Si up around 3ppm I have diatoms, when it drops below 1 ppm I get a mix. Still no algae or cyano.
I wonder if your sand sifter fish is keeping down the micrograzer inverts that could reproduce and scale up to the increased diatom growth. I mean conch snails are awesome - mine love eating diatoms off the sand - but they can't really scale up their appetite to a totally new level to match the diatom growth.