
You turn the lights on and a branch that was brown yesterday is white today. The question you have about four hours to answer correctly is whether that coral is bleached, which is survivable, or whether it is shedding tissue, which usually is not. They look similar in a photograph. They are not remotely the same problem, and the correct response to one is the wrong response to the other.
What is the difference between bleaching, STN and RTN?
Bleaching is the loss of the coral’s symbiotic algae. The tissue is still there, still alive, and has simply gone transparent so the white skeleton shows through. STN and RTN are tissue death: the tissue detaches from the skeleton and comes off, leaving bare bone. STN does it over days to weeks, RTN over hours to a couple of days. Bleached corals frequently recover. Corals shedding tissue usually do not, unless you cut ahead of it fast. Everything else in this guide follows from that single distinction, so it is worth being blunt about it: is the tissue on the skeleton, or off it?| Bleaching | STN | RTN | |
|---|---|---|---|
| What is happening | Zooxanthellae expelled or lost. Tissue intact and alive. | Tissue dying and detaching along a slow front. | Tissue sloughing off the skeleton wholesale. |
| Tissue on skeleton? | Yes — transparent, not absent | No, behind the front | No |
| Speed | Days; can be sudden after a shock | Weeks to months | Hours to about two days |
| Polyp extension | Often still present | Absent behind the front | Absent |
| Loose tissue in the water | No | Rarely, small amounts | Yes — visible sheets and strands |
| Spreads to neighbors | Only if the cause is shared | Uncommon | Often, within 24–48 hours |
| Typical outcome | Recovery over weeks to months | Salvageable if caught | Colony usually lost; frags may survive |
How do I tell if my coral is bleached or losing tissue?
Three checks, in order, and none of them need equipment. Look for the front. Necrosis has an edge — a defined line between pigmented tissue and bare white, and it moves. Bleaching does not have an edge; it fades. If you can point at a boundary and it is in a different place tomorrow, that is tissue loss. Look for polyps. A bleached coral has lost its algae, not its polyps, and will often still extend and still eat. Bare skeleton has no polyps to extend. Careful with this one though — stressed corals can stay tightly contracted for long periods, so absent polyps alone does not prove the tissue is gone. Wait a day and look for film. This is the best trick in the hobby and it comes from Eric Borneman: diatoms and algae will not settle on living coral tissue, but they colonize exposed skeleton readily and are visible within about a day. Clean white after 48 hours means tissue is still there. A brown or green haze means the skeleton is bare.The one sign that ends the argument
If tissue is visibly lifting away in sheets or strands and drifting in the flow, it is RTN. Bleaching never does this. If your skimmer starts overflowing at the same time, that is the released organic load, and you should be moving the colony out of the display before you finish reading this paragraph.How fast does RTN actually move?
Fast enough that finding it in the morning often means finding it too late. The commonly repeated figure is that RTN can strip a colony in under 24 hours, with 24 to 48 hours as the usual window. Worth being honest about where that number comes from: it is hobby convention, repeated across retailer and dip-manufacturer pages, not a figure from any published study. It matches what people report, but treat it as a rule of thumb rather than a measurement. STN is the opposite problem — it is slow enough that people talk themselves out of acting. The most useful working threshold we have seen is roughly a millimeter of recession per day or less. That is one experienced reefer’s rule rather than a consensus standard, but it gives you something to measure against instead of squinting at the colony each evening wondering whether it moved. One detail that surprises people: frags die faster than colonies. Less tissue mass, less reserve, less distance for the front to travel.What causes each one?
| Usual triggers | |
|---|---|
| Bleaching | Temperature swing in either direction; light shock, especially a coral moved up the rock or a new fixture; alkalinity swing; nutrients driven too low for the zooxanthellae to sustain themselves |
| STN | Chronic low-grade stress rather than one event: unstable alkalinity over days, sustained ultra-low nutrients, irritation at the base from neighbors or detritus, dead flow at the base |
| RTN | Acute insult: large alkalinity or salinity swing, temperature spike, stray voltage, phosphate crashed too fast by a GFO overdose, flatworm damage, shipping stress, bacterial infection |
Is RTN a bacterial infection?
Partly, and the honest answer is that this is still argued. Bacteria of the genus Vibrio are consistently associated with tissue necrosis in stony corals, and the most useful piece of science here explains something the hobby usually gets wrong — that bleaching and necrosis can be the same organism at different temperatures. Kimes and colleagues, publishing in The ISME Journal in 2012, found that Vibrio coralliilyticus is essentially harmless at or below 24 °C. Between roughly 24 and 26.5 °C it attacks the zooxanthellae, which presents as bleaching. Above 27 °C it switches on 136 virulence genes and begins lysing coral tissue outright, which presents as necrosis.
One claim worth killing
You will find pages — some of them ranking well — asserting that coral bleaching is caused by microscopic parasites. It is not. Bleaching is the loss of symbiotic algae from otherwise living tissue, which is settled science and has been for decades. The pages making that claim are generally selling something. Be careful whose diagnosis you buy alongside their treatment.What parameters should I actually be holding?
Stability matters more than the specific number in every row below. A tank held steadily at the low end of a range beats a tank that swings across the middle of it.| Parameter | Working range | The part that actually causes trouble |
|---|---|---|
| Temperature | 76–82 °F | Daily swing. Around ±1 °F is unremarkable; ±3–4 °F is a stressor. Sustained above 82 °F is where necrosis risk climbs sharply. |
| Alkalinity | 7–11 dKH; 7–8 in low-nutrient SPS systems | Rate of change. Keep it under about 0.5 dKH per day, tighter if you keep Acropora. This is aggregated hobby practice rather than a published limit, but it is the most consistently repeated number in the hobby for a reason. |
| Salinity | 34–36 ppt (1.025–1.027) | Match new water within about 0.002 SG. Top-off failures do more damage than dosing errors. |
| Nitrate | 5–50 ppm | Zero is not clean, it is starvation. Without dissolved nitrogen the zooxanthellae cannot repopulate, so a bleached coral in a zero-nitrate tank stays bleached. |
| Phosphate | 0.06–0.3 ppm | Crashing it fast with GFO is a recognized RTN trigger. Bring it down slowly or not at all. |
| PAR, Acropora | 200–300, some to 450 | Increase over weeks, never days. A coral moved up the rock is the most common self-inflicted bleaching we see. |
| PAR, LPS | Euphyllia 100–250; Trachyphyllia 50–150 | Same rule. Torches and hammers bleach from being promoted too quickly. |
What do I do right now?
If it is bleached
Find the stressor and fix that one thing. Do not correct temperature, light and chemistry simultaneously; you will add instability to an animal that is already short of reserves. Then reduce the light. This is counterintuitive and it is the single most common mistake. A bleached coral has no symbionts left to use the light, so extra intensity is pure photodamage on top of the original injury. Move it lower or shade it. Feed the tank. Dissolved nitrogen is the fuel for zooxanthellae to repopulate. A bleached coral in a zero-nutrient system has nothing to rebuild with. This is the moment to stop chasing ultra-low numbers. Do not frag it. Do not dip it. Both add stress and neither addresses symbiont loss.If it is STN
You have days, not hours, so use them to find the cause rather than reaching for treatments. Log alkalinity over several days — a single reading tells you nothing about stability. Check the base for warfare from a neighbor, for detritus, for dead flow. Gel superglue applied directly onto the receding edge halts base recession more often than it has any right to, and it buys you time. The caveat that goes with it is absolute: recession happens for a reason, and glue over an unfixed cause just moves the problem a centimeter.If it is RTN
Move fast and accept that you are trying to save a piece, not the colony.- Get the colony out of the display. RTN spreads to neighbors, frequently within a day or two. Removal comes before diagnosis.
- Cut ahead of the front, into clean tissue. Half an inch is the figure most commonly given; half a centimeter is the bare minimum anyone recommends. Give yourself the extra distance if the branch can spare it.
- Blow the loose tissue off before it becomes a bacterial substrate, and rinse the frag in clean saltwater.
- Run fresh carbon and turn the skimmer up. The dissolved organic load from a colony shedding tissue is substantial.
- Site the frags well away from wherever the mother colony was.
Does dipping help?
For RTN, mostly no, and we would rather say that plainly than sell you an expectation. Coral dips are built to kill pests — flatworms, nudibranchs, red bugs — and they do that well. They are not designed for a bacterial process already underway inside the tissue. Plenty of experienced reefers report peroxide, iodine and commercial dips all failing on an active RTN colony. Antibiotic dips have the strongest anecdotal record, and we are deliberately not publishing doses. Antibiotic use drives resistance, will destroy your biological filtration if it reaches the display, and in most places is not something a hobbyist can legally source for this purpose. If you are going down that road it is a conversation with a vet, not a blog post. Where dipping genuinely earns its place is before any of this: on every new coral, every time. Most of what triggers tissue loss walks in on a frag plug.Which corals are most at risk?
| Group | Risk | Notes |
|---|---|---|
| Acropora | Highest | First to go, every time. Thin-branched and tabling species worst. Wait until a tank is around eight months old before adding them. |
| Montipora, Stylophora, Pocillopora, birdsnest | Moderate | Tolerate 1–1.5 dKH swings and 100–150 PAR that would ruin an Acropora. Usually show slow base recession rather than sudden collapse. |
| LPS — Euphyllia, acans, favia | Lower | Bleach readily but recover well. Their equivalent emergency is brown jelly, which is a different process with a different response. |
| Softies, zoanthids, mushrooms | Lowest | They close, melt or shed, but the RTN vocabulary does not really apply. |
Will it come back?
A bleached coral with intact tissue, in a tank where the stressor has been removed and there is nitrogen available, has a genuinely good chance. Recoloring takes weeks to months and there is no reliable schedule — recovery depends on how severe the bleaching was and what conditions follow it. We have had frags come back with better color than they went in with. STN caught early is often salvageable. RTN usually is not, and the reason is worth understanding: by the time tissue is visibly sloughing, a good deal of tissue further down the branch is already dead and simply has not detached yet. That is why frags cut too close to the front keep dying. You are not fighting the front you can see, you are fighting the one you cannot.Corals that arrive already stable
Most tissue-loss events we get asked about start as shipping stress on a coral that was never adapted to aquarium conditions in the first place. Everything below is grown in our own systems in Key West under stable reef lighting, so it steps into a well-run tank rather than having to adapt to one. Oregon Tort Acropora — WYSIWYG Mini Colony$129.99 · a forgiving first Acropora, and the piece in the photo is the piece you getTUG Blue Flame Spathulata Acropora — Frag$99.99 · grown here from our own mother colonyPC Rainbow Acropora — Aquacultured Mini Colony$149.99 · WYSIWYGNot sure what you are looking at?
Send us a photo before you cut anything. We look at receding corals most weeks and would rather talk you out of an unnecessary frag than watch you lose a colony to a wrong call. Get in touch.The Underwater Gardener grows aquacultured corals in Key West, Florida (FL Aquaculture Certificate #AQ0254072). Our corals are raised under stable reef lighting in our own systems, so they arrive already adapted to a well-run tank. Corals ship UPS Next Day Air every Tuesday and Wednesday.
Sources: Kimes et al., The ISME Journal 6(4), 2012, on temperature-regulated Vibrio coralliilyticus virulence; Sweet & Bythell, Molecular Ecology, 2015, on non-specific bacterial infection and ciliate histophagy in white syndrome; Eric Borneman on bleaching versus tissue loss; Randy Holmes-Farley on optimal reef parameters and nutrient targets; NOAA Ocean Service on coral bleaching.
Knowing which coral you are looking at changes what tissue loss means — an acropora stripping and a leather deflating are not the same event. The Coral Field Guide has the structural feature that separates each genus.
Read next
Three guides that pick up where this one leaves off.
GUIDEReef Tank Water Parameters: The Numbers That Actually MatterWhere to look first when tissue starts going.Read guide New Coral Not Opening After Shipping: What’s Normal and What Isn’tWhat is normal after transit, and what is not.Read guide Coral Pests 101: How to Identify and Treat the Bugs Eating Your CoralWhen it is not chemistry — the bugs that produce the same symptoms.Read guide 
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