Short answer
Animals rely mainly on melanins, which they make, and carotenoids, which they must eat, with pterins, porphyrins and the parrots' psittacofulvins as smaller home-made classes; plants add chlorophyll, anthocyanins and betalains. Each class covers a limited range of hues, and in vertebrates blue lies outside all of them: reviews find blue to be structural in almost every case, with a single reported blue pigment cell.
Melanins are polymers built inside organelles called melanosomes. Eumelanin gives blacks and dark browns, pheomelanin gives rufous and yellowish browns, and the two mixed in different proportions cover the earth-toned range of mammal coats and many feathers. Melanin absorbs across the whole visible spectrum, more strongly at short wavelengths, so it cannot produce a saturated red, yellow, green or blue. Its usefulness goes beyond colour: it has a high refractive index, which is why stacked melanosomes serve as the reflecting layers in iridescent feathers, and feathers containing it are reported to resist wear better than unpigmented ones.
Animals cannot build carotenoids from scratch. The yellows, oranges and reds of flamingos, finches, goldfish and salmon flesh start as pigments made by plants, algae and microbes and pass up the food chain. Some are deposited unchanged. Others are chemically converted first: genetic work on red siskins and red-factor canaries implicates a cytochrome P450 enzyme, CYP2J19, as the ketolase that turns dietary yellow carotenoids into red ketocarotenoids. Binding to protein changes the colour again — the red carotenoid astaxanthin, held in the crustacyanin complex of a lobster's shell, looks dark blue, and cooking releases it as orange-red. That is the nearest most animals come to a blue made with pigment, and it is a red molecule in disguise.
Because the raw material is dietary, a captive flamingo fed without carotenoids moults into pale feathers. The colour records the last moult's diet, not today's.
Three further classes are synthesised in the body. Pterins give the whites, yellows and oranges of many butterflies' wings and the eyes and skin of various fish, amphibians and reptiles; a recent review places them between melanins and carotenoids — home-made like the first, bright like the second — and notes how little is known about their genetics. Parrots colour their red, orange and yellow feathers with psittacofulvins, a set of five pigments found in all 44 species surveyed and absent from the blood during feather growth, which points to manufacture at the feather itself. Turacos use turacin, a copper-containing porphyrin, for their crimson wing feathers: one of very few cases of a metal-based feather pigment.
Plants make all their own pigments. Chlorophyll's green comes from absorbing red and blue light for photosynthesis. Carotenoids sit beside it in the chloroplast all season and give the yellow of autumn leaves once chlorophyll is broken down. Anthocyanins, dissolved in the cell sap, supply most reds, purples and blues of flowers and fruit and shift hue with acidity and with the metal ions and co-pigments bound to them. In beetroot, cacti and their relatives in the order Caryophyllales, betalains take the anthocyanins' place; a chemistry review reports that the two classes have not been found together in one plant. Plants, unlike vertebrates, do manage blue with pigment, by modifying anthocyanins rather than by any separate blue molecule.
The observation is firm: across fishes, amphibians, reptiles, birds and mammals, blue almost always turns out to be scattered light from nanostructure. The explanation is less firm. A blue pigment must absorb strongly in the red and yellow while passing blue, which requires a different kind of molecule from the melanins, carotenoids and pterins animals already have, and it has been proposed that structure was simply the more accessible route given that every animal already makes keratin, collagen, chitin or guanine. That is an argument about evolutionary accessibility, and it has not been tested in the way a mechanism can be.
| Class | Source | Typical colours | Cannot make | Seen in |
|---|---|---|---|---|
| Melanins | Made in melanosomes | Black, brown, rufous, grey | Saturated red, yellow, green or blue | Hair, skin, most feathers, insect cuticle |
| Carotenoids | Diet in animals; made by plants and microbes | Yellow, orange, red; blue only when bound to protein | Green or violet on their own | Flamingos, finches, autumn leaves, lobster shell |
| Pterins | Made by the animal | White, yellow, orange, red | Blue or green | Butterfly wings; eyes and skin of fish, amphibians and reptiles |
| Psittacofulvins | Made at the growing feather | Yellow, orange, red | Blue or green | Parrots only |
| Porphyrins (turacin) | Made by the animal, with copper | Crimson | Blue | Turaco wing feathers |
| Anthocyanins | Made by the plant | Red, purple, blue, depending on acidity and bound ions | Yellow | Most flowers and fruit; red autumn leaves |
| Betalains | Made by the plant | Red-violet and yellow | Blue | Beetroot, cacti and other Caryophyllales |
| Organism | Structure | Mechanism | Made from | Change with angle |
|---|---|---|---|---|
| Peppered moth, dark form (Biston betularia f. carbonaria) | Wing and body scales | Pigment (selective absorption) | Melanin deposited throughout the scales. | None. Broadband absorption looks the same from every direction. |
| Greater flamingo (Phoenicopterus roseus) | Plumage, and preen-gland secretion spread over it | Pigment (selective absorption) | Carotenoids obtained from food, deposited in feathers and also present in the preen-gland secretion the bird rubs on. | None. Absorption colour; no change with angle. |
| House finch, male (Haemorhous mexicanus) | Crown, breast and rump feathers | Pigment (selective absorption) | Carotenoids taken in with the diet. | None. Absorption colour; no change with angle. |
| Red siskin and red-factor canary (Spinus cucullatus; Serinus canaria hybrids) | Body feathers | Pigment (selective absorption) | Red ketocarotenoids made from yellow dietary carotenoids by a ketolase attributed to the gene CYP2J19. | None. Absorption colour; no change with angle. |
| Parrots (Order Psittaciformes) | Red body and wing feathers | Pigment (selective absorption) | Psittacofulvins: a set of five polyenal pigments found in every species sampled and made at the growing feather. | None. Absorption colour; no change with angle. |
| Turacos (Family Musophagidae) | Wing flight feathers | Pigment (selective absorption) | Turacin, a copper complex of a uroporphyrin. | None. Absorption colour; no change with angle. |
| Lobster (Homarus spp.) | Shell | Pigment (selective absorption) | The red carotenoid astaxanthin bound in the protein complex crustacyanin, which shifts its absorption so that it looks blue. | None. Absorption colour. |
| Mandarinfish (Synchiropus splendidus) | Skin pigment cells | Pigment (selective absorption) | Cyanophores: pigment cells that produce a strong blue, in an animal group where blue is otherwise generally structural. | None. Not reported in the sources read; a pigment colour is not expected to shift with angle. |
| Red-osier dogwood (Cornus stolonifera) | Senescing leaf, upper mesophyll | Pigment (selective absorption) | Anthocyanins newly made in autumn, forming a layer above the chloroplasts. | None. Absorption colour. |
| Deciduous trees with yellow autumn leaves | Senescing leaf chloroplasts | Pigment (selective absorption) | Carotenoids present in the leaf all season, revealed when chlorophyll is broken down. | None. Absorption colour. |
| Beetroot and its relatives (Order Caryophyllales) | Roots, flowers and fruit | Pigment (selective absorption) | Betalains (red-violet betacyanins and yellow betaxanthins), which take the place of anthocyanins in these plants. | None. Absorption colour. |
Each statement is labelled by kind — established fact, a standard’s requirement, observed market data, a convention, or Colourwise’s own interpretation or analysis — with the strength of the evidence behind it.
FactStrong evidence
A survey by liquid chromatography of red feathers from 44 parrot species found the same five psittacofulvin pigments in all of them, and none in the birds' blood while feathers were growing, indicating synthesis at the feather rather than uptake from food.
Source: Distribution of unique red feather pigments in parrots
FactStrong evidence
Birds make red feather pigments by converting dietary yellow carotenoids into red ketocarotenoids, and genome comparisons of red siskins, canaries and red-factor canaries implicate the gene CYP2J19 as the enzyme responsible.
Caveat: The enzyme's role is inferred from introgression and expression data in these finches.
FactStrong evidence
The red pigment of turaco wing feathers, turacin, is a copper complex of a uroporphyrin.
FactStrong evidence
Melanin has a high refractive index as well as broadband absorption, which allows melanosomes to act as optical building blocks in structural colours in addition to colouring tissue directly.
Source: Melanosomes: biogenesis, properties, and evolution of an ancient organelle
FactStrong evidence
Betalains replace anthocyanins in most families of the order Caryophyllales, and the two pigment classes have not been found together in the same plant.
Colourwise interpretationLimited evidence
The rarity of blue pigment in animals is better described as an observed pattern than as an explained one: the suggestion that structure was the more accessible evolutionary route is plausible but untested.
Based on: The review documents the pattern across vertebrate classes; Colourwise found no cited experiment or comparative analysis that tests why pigmentary blue did not evolve.
Caveat: Absence of a test is not evidence against the suggestion.
Reviewed 6 October 2026. Colourwise summarises its sources in its own words and does not reproduce standards text or proprietary colour data. Spotted an error? Tell us.