Gaildunningite

The kinds of rock environments where the mineral typically forms — igneous, metamorphic, hydrothermal, sedimentary, pegmatitic, and so on.

The place where the mineral was first found and described — by convention, the reference point for the species.

Resistance to being scratched, ranked on the Mohs scale from 1 (talc, marked by a fingernail) to 10 (diamond, scratches everything below it). The classic field test.

Whether and how much light passes through a mineral, from transparent (you can see through it) to translucent, then opaque.

The hue of the mineral itself. Often unreliable for identification — many species occur in several colours depending on trace impurities or radiation damage.

The colour of a mineral's powder, drawn by scraping it across an unglazed porcelain plate. Far more consistent than surface colour.

How a mineral resists breaking, bending, or crushing. Brittle snaps cleanly, malleable hammers into sheets, sectile slices like soft metal.

The tendency to split along flat planes that match the crystal's atomic structure. Described by quality (perfect, good, poor) and direction.

The shape of a broken surface that doesn't follow cleavage — conchoidal (curved, like broken glass), uneven, hackly, or splintery.

Mass per unit volume, in grams per cubic centimetre. A useful sorting tool: barite is twice as dense as quartz at the same size.

A change of colour as a coloured anisotropic mineral is rotated under plane-polarised light. Tourmaline and cordierite are textbook examples.

The colour seen through a polarising microscope — often unlike the hand-specimen colour, because section thickness and orientation both matter.

A visible change in reflectance as an opaque mineral is rotated under plane-polarised reflected light. Diagnostic for ore minerals.

Coloured glints from inside an opaque mineral, seen when light reaches translucent zones beneath the polished surface.

How the mineral glows under short- and long-wave ultraviolet lamps. Some species fluoresce in spectacular colours invisible to the naked eye.

One of seven geometric families that describe a mineral's atomic symmetry: isometric (cubic), tetragonal, hexagonal, trigonal, orthorhombic, monoclinic, triclinic. Two non-crystalline classes — amorphous and icosahedral — also appear.

The lengths of the unit-cell edges (a, b, c) in ångströms — the smallest repeating box of atoms that builds the crystal.

Edge-length ratios of the unit cell, normalised so b = 1. Lets you compare related species without quoting absolute ångström values.

The number of formula units contained in a single unit cell.

Two or more crystals of the same species grown in a fixed symmetric relationship, sharing a plane or axis. Often visible as re-entrant angles.

Splitting along planes of weakness that aren't true cleavage — usually caused by twinning or solid-state pressure.

The crystal habit observed at the type locality — the place where the mineral was first described.

Chemical elements that make up the mineral's ideal formula, listed by atomic symbol with their share of the total mass.