Psilocybe subaeruginosa, a wood-degrading magic mushroom that produces the psychedelic compound psilocybin, is structured by geography across its Australian range, but geographically separated populations remain fully sexually compatible. Genetic analyses of 89 isolates show that allelic diversity at mating compatibility and psilocybin loci likely results from genetic drift and minimal gene flow since divergence from a common ancestor. Movement of woodchips, mulch, or plants has probably spread genotypes locally within Australia and to the northern hemisphere. Northern-hemisphere species P. azurescens and P. cyanescens cluster among Australian populations, suggesting they are the same species as P. subaeruginosa, whose centre of origin is Australasia. High allelic diversity occurs in psilocybin pathway genes, with some haplotypes carrying one or two putatively functional copies of psiH, though the duplication's functionality remains unknown.
Some entomopathogenic fungi keep their insect hosts alive while releasing spores, a behavior that improves spore dispersal. Metabolomics of four populations of periodical cicadas infected with Massospora cicadina revealed the plant-associated amphetamine cathinone, while annual cicadas infected with Massospora platypediae or Massospora levispora contained the mushroom-associated tryptamine psilocybin; the latter two fungi appear to be a single species. The absence of certain fungal enzymes needed to produce cathinone and psilocybin, along with undetectable intermediate metabolites or gene orthologs, suggests novel biosynthesis pathways in Massospora. The neurogenic activity of these compounds indicates that the extended phenotype of Massospora, which alters cicada behavior to maximize spore dissemination, is chemically induced.