Amanita australis

Amanita australis was first described by Greta Stevenson in 1962, based on specimens she collected in April 1954 around Lake Rotoiti in Nelson Lakes National Park, in New Zealand. In the same publication, Stevenson described Limacella macrospora, collected in 1952 at Day's Bay near Wellington. Stevenson thought this was a new species different from any previously described Limacella because of its larger size and amyloid spores. ==Description==

The shape of the A. australis cap is initially convex, later flattening out or even developing a central depression, and reaching diameters of wide. The cap margin sometimes splits and rolls back to give a ragged appearance. The centre of the cap is dark buff, honey or isabelline, becoming paler to buff at the margin. The surface is sticky when young or wet, but dries out with age. The remnants of the volva form conical to pyramidal warts that are most densely aggregated in the center, but become sparse and low towards the margin. They are initially white then greyish-sepia or isabelline with white to buff tips. The gills are crowded closely together, free from attachment to the stem, wide, and white. The lamellulae (short gills that do not extend fully from the cap edge to the stem) have truncated ends. The stem is tall, in diameter, and narrowest at center. It is hollow, and has an abruptly bulbous base that is between in diameter. The surface of the stem above the level of the ring is white and covered in woolly tufts of mycelia; below the ring it is white with buff to greyish transverse, grooved bands. The base may or may not have a rim of volval remnants that are powdery, and a greyish-buff to greyish-sepia colour. The ring is membranous, white to buff, first hanging freely then later adhering to the stem. The flesh of the cap is white, occasionally pale isabelline under the center of the cap; the flesh of the stem is white. The spore print is white. The spores are typically 9–12 by 8–10.5 μm, spherical to ellipsoid, and thin-walled. They are hyaline (translucent), and amyloid—meaning they will stain bluish-black to black in Melzer's reagent. The basidia are 43.5–76.5 by 10.5–17 μm, mostly four-spored, and clamped at their bases. There are abundant spherical, elliptic or club-shaped hyaline cells on the gill edges, measuring 16–39.5 by 10.5–27.5 μm. The cap cuticle is 220–270 μm wide, consisting of a gelatinised suprapellis (upper layer) and non-gelatinised subpellis (lower layer). The volval remnants on the cap consist of abundant spherical, club-shaped, or turnip-shaped cells, measuring 10–86 by 9–85 μm. These cells are umber in colour, and arranged in chains perpendicular to the cap surface, becoming smaller and paler at tip of the wart, subtended by moderately abundant hyphae that are 4–10 μm wide. Clamp connections are abundant in the hyphae. Similar species A. australis mushrooms that have lost their warts and have had the colours faded may resemble another New Zealand species, A. nothofagi. The two species may be distinguished reliably using microscopy—A. nothofagi does not have clamp connections at the base of the basidia, unlike A. australis. A. australis also bears some resemblance to the eastern North American and east Asian species A. abrupta, which also has an abruptly bulbous stem base. ==Distribution and habitat==

A. australis is found only on the north and south islands of New Zealand, where it grows in a mycorrhizal association with southern beech (genus Nothofagus) (including New Zealand red beech, silver beech, New Zealand black beech, hard beech), mānuka, and Kānuka. The mushroom usually grows solitarily, but has on rare occasions been found growing in groups. ==See also==