Orcus Varuna
New member
Sometimes internet trolling is just too much fun.... [MENTION=286110]Bpb[/MENTION] bubble scrubbing eliminates red bugs? Right?
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In all seriousness here. Orcus Varuna, and some other friends were discussing this. I expected there would be HEAVY disagreement, and even some eye rolls and perhaps some catty comments. I can handle those. I dish them out plenty.
Much like the "œway too soon," and "œway too bold" predictions that college football analysists make in the off season, I'll make my own.
Way too bold statement
Nano Bubble Scrubbing Cured my red bug infestation.
I'm not a doctor, PhD, or a specialist in any scientific field, but I consider myself a learned man of sorts. And I am familiar with the saying "œcorrelation does not denote causation." I realize that the skeptic will say "œjust because you began nano scrubbing and the bugs disappeared, does not mean the nano scrubbing cured them".
But....all the same.
I have had a wicked acro red bug infection for the greater part of the last year. Virtually zero PE on anything and poor colors (which I may have unfairly blamed on lighting, I'll admit). After 8, yes 8 rounds of double strength interceptor, the bugs prevailed. I decided to just live with them.
Enter nano scrubbing. I know I'm late to the party on this one but I decided to hop on board. 6-8 weeks in now, and I cannot find a single red bug. Matter of fact I haven't seen a single one in over a month. And I've been zooming with macro lenses. Looking daily. Not a single red bug to be found. And the PE I'm getting now is tremendous. Polyps out in acros I had never seen them on.
So my hypothesis is this. The nano scrubbing has created such a heavy nightly sliming event that the acros have physically shed the red bugs in sufficient numbers that the wrasses have picked them off or they've died without their host. And it has happened to enough of a degree that they've failed to reproduce any further.
Discuss.
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I have some questions on this whole concept.
-First what is the goal, bubbles in general or an increase in DO?
-does anyone else check their DO? Mine runs pretty high to begin with (7- 7.5) anyone willing to compair? Would super saturated be any better or worse?
- could this be achieved with a o2 reactor? Just a canaster with a fan and o2 beeing run through with water the same as a basic co2 reactor. But maybe more efficient? Maybe 24-7 but at a lower nonvisable rate during viewing hours (less swing=more stability is usually good for a reef)?
-has anyone dropped their temp or salinity slightly to maximize the effects? Not daily just slowly dropped to a slightly lower temp and/or salinity.
-Maybe try this in a qt with hyper for beginning stages of parasites and such to promote healing naturally?
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Oh I understand the slime acropora red bug connection..In my observation. It's only the stonies that slime. I've not observed it in any other species I keep (acans, leptastrea, zoas, Gorgonians, lobophyllia, aiptasia lol). I don't think I'd REPLACE a regular quarantine with it, but definitely use it in conjunction with regular medications.
I mention the acropora sliming so specifically because red bugs are an acropora specific parasitic copepod that aren't known to inhabit any other genus of coral
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Yes I would think the same, but I do have 3 very active wrasses that I would not be the least bit surprised if they were preying on them. I can sit there and watch my sixline wrasse hover over a colony like a search and rescue chopper and just pick them off with surgical precision.
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[MENTION=286110]Bpb[/MENTION]
Do you have experience with flatworm exit? This is what I've been using to dip and with a turkey baster, it's worked for flatworms in general but do you know if aefw are any different? Generally I do a concentrated dip and blow the mix into all nooks and crannies and if there are worms they fall out and start dieing immediately. Then move the piece to untreated qt. I've yet to have them reappear after this but I still do a second dip a week later. I also generally don't deal with the source once I have issues like this.
So I know we practice different things than we recommend at times . my thinking was that maybe between this an inteceptor dip and a general iodine type dip and then adding bubble to the uuntreated qt I could be relatively sure I'm avioding coral pests at which point it could be added to a fallow system or you roll the dice on fish parasites depends on preference I guess.
Not looking for a recomendation, just sharing though process. My thoughts were more that if bubbles=slime and shedding, in a small closed qt system you should really notice if there are or aren't redbugs pretty quick if their getting knocked off all the time espically of you did the initial dip and didn't find any.
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Yes.. can't underestimate the predators. I recently added two baby yellow wrasses- about 1 1/2 inches. I have never seen two more active acropora scavengers..
I've had adult yellow wrasses that were not nearly as active at picking over acropora.
Fish alter their behavior as they mature.. I'm wondering if this may be part of the missing link in aquariums..
In the wild there is a constant supply of everything from tiny to large predators. The tiny ones being more capable and perhaps more interested in getting in amongst the branches of corals... in any given aquarium, we only have certain predators at a certain level of maturity..
Bob, can you detail your full method for using and producing the micro-bubbles?
How much time elapsed between the use of interceptor and the start of the bubbling? It seems possible that you disrupted their ability to reproduce and the bubbles had nothing to do with it...