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Lesson 11 / 18 · Compost Operator

Ammonia

Ammonia is the commonest reason a good looking batch kills its spawn. Removing it is not the hard part. Proving it has gone is.

  • By the end you can say where the ammonia in a batch came from.
  • By the end you can explain why smell is not a measurement.
  • By the end you can ask the four questions before calling compost ready.

From symptom to cause

A first look, not a diagnosis. Source: ICAR-DMR manual and disease bulletin.

What you seeLikely causeFirst step
Long stems, small capsCO₂ too high (above about 1,500 ppm)More fresh air
Green patches on compostTrichoderma; low pH or leftover ammoniaIsolate, remove; check next batch
No pins after casingRoom not aired and cooled16 to 18 °C, ventilate
Brown sunken spots on capsBacterial blotch; wet capsDry the surface, humidity under 85%
White wet lumpsWet bubble from casingSalt, remove; steam next casing
Small fliesSciarid or phorid fliesScreens, light traps, hygiene

Read numerical examples with their source, method and crop context. They are not universal operating instructions. Historical prices are not current quotations.

Ammonia after Phase I800 to 1,000ppmMeasured before Phase II, alongside pH 8.2 to 8.5Source: ICAR-DMR manual, 2011
Ammonia limit at spawning8 to 10ppmDMR: normally not more than 8 to 10 ppm at spawningSource: ICAR-DMR manual, 2011
Smell detection floor10ppmBelow this the nose generally cannot detect ammonia at allSource: ICAR-DMR manual, 2011
Formulation nitrogen at stacking1.5 to 1.75percent dry weightAbove 1.75 percent, more nitrogen is lost as ammonia and yellow moulds followSource: ICAR-DMR manual, 2011
Conceptual cutaway of a compost conditioning tunnel with material above an air plenum.
AI-generated teaching illustration · not field evidence
Connect the picture to the lesson

Understand the tunnel

Notice
Air must pass through the loaded material.
Understand
Pasteurisation, conditioning and cooling have distinct purposes.
Try it
Use the validated process and release criteria, not an odour test.
See where this fits in the full workflow →

01Where it comes from

Ammonia is nitrogen on the move. Urea, chicken manure, cotton seed cake and every other nitrogen source breaks down during Phase I, and the nitrogen leaves the material as ammonia. This is normal. DMR reports compost at the end of Phase I holding about 800 to 1,000 ppm, with pH pushed up to roughly 8.2 to 8.5.

The size of your ammonia problem is therefore decided long before the tunnel. DMR notes that a mix carrying more than 1.75 percent nitrogen loses more of it as ammonia, and that such compost attracts yellow moulds, ink caps and olive green mould.

02Smell is not concentration

DMR states plainly that we generally cannot smell ammonia below 10 ppm. Read that carefully. Your nose can tell you ammonia is present. It can never tell you the level is low enough. Those are different statements, and crops are lost on the difference.

A nose also tires. After a few minutes in the corridor you stop noticing a smell that has not changed. That is olfactory fatigue, and it makes the second sniff less reliable than the first. Never deliberately breathe compost air to test a batch. Ammonia is an irritant gas and a tunnel is a confined space.

03Four questions before you decide

When someone reports that the compost still smells of ammonia, do not reach for a chemical and do not add a day. Ask four questions first, because each one changes the answer.

Which stage is this: end of Phase I, mid conditioning or after cooling? What method produced the reading: an instrument, a detector tube or a nose? Where was the sample taken: front, back, top, middle or plenum? Has cooling started, since a warm mass releases ammonia that a cooled mass holds back? A reading without those four facts cannot support a spawning decision.

  • Stage
  • Method
  • Sample location
  • Cooling status

04What it looks like after spawning

If ammonia is still there at spawning, the compost tells you within days. Spawn runs slowly or stops in patches. DMR lists ink caps, the black inky Coprinus mushrooms, under presence of ammonia and high nitrogen in compost. It ties Oedocephalum mould to ammonia and amines that were not eliminated during pasteurisation and conditioning.

By then nothing in that batch can be repaired, so the lesson belongs to the next one. Check the formulation nitrogen you actually stacked, the oxygen supply during conditioning, and whether your ammonia evidence was honest or convenient.

Build an honest ammonia record

  1. Write down the nitrogen sources and weights you actually stacked, not the recipe.
  2. Fix three sampling points in the tunnel and use the same three every batch.
  3. Record the test method by name and keep it unchanged across batches.
  4. Note compost temperature and whether cooling had started at each test.

Write in your farm diary: Date, stage, method, the three points with their readings, and the decision taken on that evidence.

Mistakes that cost a crop

  • Treating the nose as an instrument, when DMR uses it only to say ammonia is present.
  • Sampling the one convenient point near the door and calling the whole tunnel clear.
  • Adding a fixed extra day of conditioning instead of finding why ammonia is not clearing.

Check yourself

Three questions, instant answers
  1. A worker says the tunnel smells clean, so ammonia is below 10 ppm. This is:

  2. Ink caps after spawning point mainly to:

  3. Besides stage, method and cooling status, a reading needs:

An editorial self-check, not a certificate. Answers are not stored, not even on this device.

Words used in this lesson

ppm
Parts per million. Ten ppm is ten parts of ammonia in a million parts of air.
Olfactory fatigue
The nose stops noticing a steady smell after a few minutes.
Ink cap
Coprinus, a fast black weed mushroom that signals ammonia in compost.
References & further reading
Button mushroom compost knowledge system

A lesson cannot replace batch measurements or plant-specific procedures.

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