Arsenopyrite

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

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.

How the mineral's surface reflects light — from metallic and glassy to silky, pearly, or dull. Often the first clue to identification in the field.

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.

Whether an opaque mineral changes brightness or hue as the stage is rotated under crossed polarisers in reflected light. A key ore-mineral test.

A general label for how an opaque mineral responds to polarised reflected light, summarising bireflectance and anisotropism together.

The percentage of incident light reflected by a polished surface, measured at standard wavelengths. The defining property of ore microscopy.

Emission of visible light triggered by an external energy source — UV, heat, friction, or impact. Includes fluorescence and phosphorescence.

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 full symmetry description of a crystal's repeating atomic pattern — 230 distinct groups, written in Hermann–Mauguin notation (e.g. P6₃/mmc).

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

The angles (α, β, γ) between unit-cell edges, in degrees. Cubic crystals have 90°/90°/90°; triclinic crystals can take any combination.

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

Volume of the unit cell in cubic ångströms (ų). Reflects how tightly the atoms are packed for a given chemistry.

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

The overall shape and habit a mineral tends to grow into — cubes, prisms, plates, fibres, druses, masses.

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.

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

Minor or trace elements outside the ideal formula but commonly detected in natural specimens. Often the cause of colour variation.