Twenty-four species of rust fungi known from Auckland Islands and Campbell Island are listed, together with details of their host plants. Several species are recorded for the first time in these subantarctic islands. Four species are newly described and illustrated, viz., Milesia polystichi-vestiti on Polystichum vestitum (Dryopteridaceae), Petersonia dracophylli on Dracophyllum longifolium (Epacridaceae), Puccinia austrina on Isolepis habra (Cyperaceae), and Puccinia chathamica on Carex trifida (Cyperaceae). Uredo inflatus is transferred to Uromyces (as Uromyces inflatus comb. nov.) following recognition of the spores on Anisotome latifolia (Apiaceae) as teliospores.

As the first report of monographic studies of the genus Phyllosticta in Japan, four new species, Phyllosticta disanthi on Disanthus cercidifolius, P. hoveniicola on Hovenia dulcis, P. ligustricola on Ligustrum obtusifolium, and Phyllosticta alliacea on Allium fistulosum, are described and illustrated. A new teleomorphic state of P. alliorum, Guignardia alliacea, is confirmed.

Structure and ornamentation of basidiospore walls in Xerula (inclusive of Dactylosporina) are illustrated using scanning electron microscope (SEM) images. Oudemansiella spores are not depicted, but all sections of Xerula are represented by 17 taxa. Spore wall sculpturing cannot be used as an infrageneric diagnostic character, nor to separate Oudemansiella and Rhizomarasmius from Xerula. Xerula caulovillosa is proposed as a new species, and Xerula radicata f. marginata as a new combination.

The ultrastructure of developing basidiospores in Rhizopogon roseolus is described. When viewed in the fruiting body chamber using scanning electron microscopy, basidiospores appear narrowly ellipsoid and have smooth walls. Eight basidiospores are usually produced on the apex of each sterigma on the basidium. Transmission electron micrographs showed that basidiospores formed by movement of cytoplasm (including the nuclei) via the sterigmata, and then each basidiospore eventually became separated from its sterigma by an electron-lucent septum. The sterigma and basidium subsequently collapsed, resulting in spore release. Freshly released spores retained the sterigmal appendage connected to the collapsed basidium. After spore release, the major ultrastructural changes in the spore concerned the lipid bodies and the spore wall. During maturation, lipid bodies formed and then expanded. Before release, the spore wall was homogeneous and electron-lucent, but after release the spore wall comprised two distinct layers with electron-dense depositions at the inner wall, and the dense depositions formed an electron-dense third layer. The mature spore wall complex comprised at least four distinct layers: the outer electron-lucent thin double layers, the mottled electron-dense third layer, and the electron-lucent fourth layer in which electron-lucent granular substances were dispersed.

To investigate the quantitative correlation between dynamics of ectomycorrhiza (ECM) formation and fruit-body production of the ammonia fungi, we treated forest soils in two ECM forests, a Castanopsis cuspidata forest and a Quercus serrata forest, in warm temperate Japan with urea to induce fruiting of ammonia fungi. We identified the ectomycorrhizae of two known species of ammonia fungi, Alnicola lactariolens and Hebeloma vinosophyllum, using morphological typing and PCR-RFLP. ECM initiation, increase, and subsequent decrease preceded the start, increase, and decrease of fruit-body production for each species. We also found many kinds of ECM fungi that did not develop fruit bodies after urea treatment during the observation period, which suggests that it is necessary to expand the definition of ammonia fungi from one that refers solely to the species reproducing on the ground to one which includes those in somatic forms in the soil.

I report seven species of Wrightoporia, including one undetermined species and one Taiwanoporia sp., collected in Japan. The following species are newly described: Wrightoporia aurantipora, W. labyrinthina, W. straminea, and Taiwanoporia roseotincta. Wrightoporia avellanea and W. lenta are newly reported for Japan. A detailed description is also provided for W. japonica, a poorly known species described from Japan. Wrightoporia aurantipora is characterized by the resupinate basidiocarp, orange-tinted pores, skeletal hyphae with restricted dextrinoid reaction, and lack of gloeoplerous hyphae. Wrightoporia labyrinthina is characterized by the resupinate basidiocarps, labyrithiform hymenophore, and abundant gloeoplerous hyphae. Wrightoporia straminea is characterized by the resupinate basidiocarps, the skeletal hyphae with restricted dextrinoid reaction, and SV+ cystidia. Taiwanoporia roseotincta is characterized by the sappy and pinkish-white basidiocarps and monomitic hyphal system without clamp connections.

Heteroecious Phakopsora euvitis, P. vitis, and P. ampelopsidis, autoecious P. meliosmae, and an unconnected Aecidium on Meliosma are closely allied. A total of 45 collections representing the five rust fungi from Japan, Australia, and East Timor were subjected to molecular phylogenetic analyses: the D1/D2 region of nuclear large subunit rDNA and nuclear small subunit internal transcribed spacer 2 (ITS2) region including 5.8S rDNA were analyzed. Tree topologies generated from parsimony and distance methods of the D1/D2 and ITS2 sequences were similar. The 45 collections (44 for ITS2 and 33 for D1/D2, with 32 common for both analyses) are grouped into seven clades: P. ampelopsidis, P. vitis, unconnected Aecidium, P. euvitis from Japan, P. euvitis from Australia and East Timor, P. meliosmae on M. myriantha, and P. meliosmae on M. tenuis. The results confirm the phylogenetic distinctness of P. euvitis, P. ampelopsidis, and P. vitis distributed in Japan. A grapevine leaf rust fungus in Australia and East Timor has genetically diverged from P. euvitis in Japan. The unconnected Aecidium is highly likely to be an aecial anamorph of a Phakopsora fungus. Autoecious Phakopsora fungi on M. meliosmae and M. tenuis need further host-specificity and morphological studies to confirm their taxonomic status.

The Chinese Bai-Ling-Gu is a mushroom named Pleurotus eryngii var. tuoliensis C.J. Mou. This species has been identified as P. nebrodensis or P. eryngii var. nebrodensis. We examined its taxonomic position by analysis of mating, cultivation, and rDNA sequences, and concluded as follows. (1) Bai-Ling-Gu mated with P. eryngii var. eryngii, and the F₁ and F₂ formed fruit bodies. (2) Bai-Ling-Gu mated with P. eryngii var. ferulae, and the F₁ formed fruit bodies. (3) In the di-mon mating test, P. eryngii var. nebrodensis from Sicily mated with monokaryons of P. eryngii var. eryngii but mated hardly at all with those of Bai-Ling-Gu and P. eryngii var. ferulae. The di-mon mating pattern of Bai-Ling-Gu resembled those of P. eryngii var. ferulae. (4) The partial sequences of rDNA ITS1 and IGS1 from the epitype of P. nebrodensis were identical with those from P. eryngii var. nebrodensis from Sicily but differed from those from Bai-Ling-Gu. (5) The strains of P. eryngii var. eryngii and P. eryngii var. ferulae were in a group, the strains of P. eryngii var. nebrodensis from Sicily were in another group, and the strains of Bai-Ling-Gu were in the other group in both the phylogenetic trees based on the ITS1 and the IGS1 sequences. These results led to the conclusion that Bai-Ling-Gu is a variety of P. eryngii and evolved independently in China. It is satisfactory to identify Bai-Ling-Gu with P. eryngii var. tuoliensis C.J. Mou.

The Japanese common edible mushroom called “nameko” at present is a species belonging to Pholiota. This species has been identified as P. nameko (T. Ito) S. Ito & Imai (= Collybia nameko T. Ito, 1929). The type specimens of C. nameko are not traced in herbaria. The plate of the original description is designated as the lectotype of C. nameko T. Ito. The Himalayan species P. microspora (Berk.) Sacc. (= Agaricus microsporus Berk., 1850) is identical with “nameko.” The author concludes P. nameko is a synonym of P. microspora.