Agent-almanac fungi-identification

install
source · Clone the upstream repo
git clone https://github.com/pjt222/agent-almanac
Claude Code · Install into ~/.claude/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/pjt222/agent-almanac "$T" && mkdir -p ~/.claude/skills && cp -r "$T/i18n/caveman/skills/fungi-identification" ~/.claude/skills/pjt222-agent-almanac-fungi-identification-24d86a && rm -rf "$T"
manifest: i18n/caveman/skills/fungi-identification/SKILL.md
source content

Fungi Identification

Identify fungi in the field using morphological features, spore prints, habitat, and season with an absolute safety-first approach.

When to Use

  • You encounter an unknown fungus and need to identify it
  • You are foraging for edible mushrooms and need to confirm species before consumption
  • You want to assess whether fungi in your garden or property are harmful
  • You are building field identification skills through structured observation practice
  • You need to differentiate an edible species from a dangerous look-alike

Inputs

  • Required: A fungus specimen or clear observation of one in situ
  • Required: Ability to observe fine morphological details (cap, gills, stem, base)
  • Optional: Field guide or reference material for the region
  • Optional: Paper and glass for spore prints
  • Optional: Knife for cross-section examination
  • Optional: Hand lens (10x) for fine detail

Procedure

Step 1: The Cardinal Rule

Before any identification work, internalize the absolute rule of mycology.

CARDINAL RULE:
If you are not 100% certain of the identification, DO NOT EAT IT.

There is no "universal edibility test" for mushrooms.
Some deadly species taste pleasant.
Some deadly species have delayed symptoms (24-72 hours).
Some deadly species have NO antidote.

The cost of a false positive (eating a misidentified mushroom) is
organ failure and death. The cost of a false negative (skipping an
edible mushroom) is a missed meal.

ALWAYS ERR TOWARD CAUTION.

Expected: The cardinal rule is internalized before proceeding with identification.

On failure: There is no failure mode for this step. If the rule is not internalized, do not proceed to field identification for consumption purposes.

Step 2: Document the Habitat

Context narrows identification before touching the specimen.

Habitat Recording:
+--------------------+------------------------------------------+
| Factor             | Record                                   |
+--------------------+------------------------------------------+
| Substrate          | Soil, wood (dead/living), dung, leaf      |
|                    | litter, moss, other fungi                |
+--------------------+------------------------------------------+
| Tree association   | What trees are within 10m? (Many fungi    |
|                    | are mycorrhizal with specific tree genera)|
+--------------------+------------------------------------------+
| Moisture           | Dry, damp, wet, waterlogged              |
+--------------------+------------------------------------------+
| Light              | Full shade, dappled, open                |
+--------------------+------------------------------------------+
| Season             | Early spring, late spring, summer, early  |
|                    | autumn, late autumn, winter              |
+--------------------+------------------------------------------+
| Altitude           | Lowland, mid-altitude, montane           |
+--------------------+------------------------------------------+
| Growth pattern     | Solitary, scattered, clustered, ring,    |
|                    | shelf/bracket                            |
+--------------------+------------------------------------------+

Expected: A complete habitat record that provides context for species-level identification.

On failure: If habitat is unclear (e.g., urban garden with mixed plantings), record what is visible. Incomplete habitat data reduces identification confidence — factor this into the safety assessment.

Step 3: Examine Morphological Features

Systematic examination of the specimen itself.

Morphological Checklist:

CAP (Pileus):
- Shape: convex, flat, concave, conical, umbonate, bell-shaped
- Diameter (measure or estimate)
- Surface: smooth, scaly, fibrous, slimy, dry, cracked
- Colour (note if colour changes with age or moisture)
- Margin: smooth, striate, inrolled, appendiculate (veil remnants)

GILLS / PORES / SPINES (Hymenium):
- Type: gills (lamellae), pores (tubes), spines (teeth), smooth
- Attachment: free, adnexed, adnate, decurrent
- Spacing: crowded, close, distant
- Colour (important — note changes with age)
- Bruising: do gills change colour when damaged?

STEM (Stipe):
- Height and diameter
- Shape: equal, tapered, bulbous, club-shaped
- Surface: smooth, fibrous, scaly, reticulate (netted)
- Interior: solid, hollow, stuffed (pithy center)
- Ring (annulus): present/absent, position, persistent/fragile
- Volva (cup at base): present/absent — ALWAYS check by
  carefully excavating the base (Amanita species have a volva)

FLESH (Context):
- Colour when cut
- Colour change on exposure to air (note time to change)
- Texture: firm, brittle, fibrous, gelatinous
- Smell: mushroomy, anise, radish, flour, chlorine, unpleasant
- Taste: (ONLY if species is confirmed non-deadly by an expert;
  for unknown species, DO NOT taste)

SPORE PRINT:
- Remove the stem; place the cap gill-side down on paper
  (half white, half dark paper to see any colour)
- Cover with a glass or bowl to maintain humidity
- Wait 4-12 hours
- Record spore colour: white, cream, pink, brown, purple-brown,
  black, rust-orange

Expected: A complete morphological description covering all major features.

On failure: If a feature cannot be observed (e.g., no ring visible but it may have been lost), record it as "not observed" rather than "absent." The distinction matters for identification.

Step 4: Identify Using Multiple Confirmations

Cross-reference all data against reference material.

Identification Protocol:
1. Use habitat + season to narrow to likely genera
2. Use cap shape + gill type + spore colour to narrow to species group
3. Check ALL features against the candidate species description
4. Specifically check against dangerous look-alikes:
   - Does this species have a deadly doppelganger?
   - What feature distinguishes the edible from the deadly?
   - Can I see that distinguishing feature clearly?

Confidence Levels:
+----------+---------------------------+---------------------------+
| Level    | Criteria                  | Action                    |
+----------+---------------------------+---------------------------+
| Certain  | All features match; no    | Safe to collect (for      |
|          | look-alike confusion;     | experienced identifiers)  |
|          | experienced with species  |                           |
+----------+---------------------------+---------------------------+
| Probable | Most features match;      | DO NOT eat. Collect for   |
|          | one or two uncertain;     | further study (spore      |
|          | look-alike eliminated     | print, expert review)     |
+----------+---------------------------+---------------------------+
| Possible | Some features match;      | DO NOT eat. Photograph    |
|          | look-alike not fully      | and seek expert opinion   |
|          | eliminated                |                           |
+----------+---------------------------+---------------------------+
| Unknown  | Cannot narrow to species  | DO NOT eat. DO NOT        |
|          |                          | handle extensively        |
+----------+---------------------------+---------------------------+

Expected: A species-level identification with explicit confidence level and look-alike assessment.

On failure: If identification stalls at genus level, that is acceptable for learning purposes. For consumption, only species-level "Certain" identification is acceptable.

Validation

  • The cardinal rule was acknowledged before starting identification
  • Habitat was documented before examining the specimen
  • All morphological features were examined systematically
  • The base was excavated to check for a volva
  • A spore print was taken (if time allows)
  • Dangerous look-alikes were explicitly checked and eliminated
  • Confidence level was honestly assessed
  • Only "Certain" identifications were considered for consumption

Common Pitfalls

  • Relying on a single feature: "It looks like a chanterelle" based on colour alone. True chanterelles have false gills (ridges), grow from soil near trees, and have a specific apricot smell. False chanterelles and Jack-o'-lanterns share the colour but differ in every other feature
  • Skipping the base examination: Failing to dig up the base misses the volva — the single most important feature for identifying deadly Amanita species (death cap, destroying angel)
  • Trusting apps blindly: AI-based mushroom identification apps have significant error rates for look-alike species. Use them as a starting point, never as confirmation
  • Assuming "common = safe": Abundance does not indicate edibility. Deadly species can be locally abundant
  • Tasting unknown species: Some mycologists use taste as a diagnostic tool, but this requires expert-level knowledge of which species are safe to taste. For non-experts, do not taste unknown fungi
  • Ignoring temporal toxins: Some species (e.g., Amanita phalloides) have pleasant taste and delayed symptoms. By the time symptoms appear (24-48 hours), liver damage is severe

Related Skills

  • mushroom-cultivation
    — growing known species eliminates identification risk entirely
  • forage-plants
    — complementary field identification skill; shares the multi-feature confirmation methodology