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Horak, E. 1971: A contribution towards the revision of the Agaricales (Fungi) from New Zealand. New Zealand Journal of Botany 9(3): 403-462.
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Agaricus campestris (Linne) (1,16) = Agaricus campester Fries. Material: COLENSO, New Zealand. Apparently introduced like other coprophilous fungi.

Agrocybe vervacti (Fries) (6) = Galerina sp.

All characters observed in the collection (COLENSO b 71) clearly indicate that this fungus must be placed in Galerina, it being one of the most common species of this genus in New Zealand.

Apparently introduced with exotic trees such as Quercus or Picea.
Provided that the identification is correct, this species must be considered as having been introduced into New Zealand with exotic trees such as spruce or fir.
This conspicuous species occurs in New Zealand under various exotic trees where it forms mycorrhizas, and there is no question that this agaric is an introduced species. However, like Stevenson (25), we found many fruiting bodies of this species in native bush with Nothofagus and Leptospermum. It would be interesting to know if this introduced mycorrhizal fungus can change its host and form partnerships with these two indigenous genera which normally form ectotrophic mycorrhizas with numerous indigenous Agaricales. The wide host range of A. muscaria sugests that this possibility is not unlikely.
Two collections exist at Kew: one (COLENSO b 286) undoubtedly represents Collybia novae-zelandiae (Stevenson) Horak and the other (COLENSO b 331) belongs to a variety of A. vaginata which will be described along with others in a separate publication.
The spores are much too small (13-17 X 9-11 µ) for this specimen (COLENSO b 806) to be conspecific with the coprophilous A. fimiputris. Cystidia are absent.
No material of this coprophilous agaric is preserved, but it is very likely that this occasionally introduced fungus grows here and there in New Zealand.
A critical study of the N.Z. species of Armillariella is being undertaken by McNabb. Our personal observations indicate that there are several native species besides the introduced A. mellea, which is a common but disliked parasite in the exotic forests of this country.
According to Singer (1969) this species was also collected in the Nothofagus forests of South America.

Collybia readii Stevenson (29 D) Fig. 23 = Calocybe readii (Stevenson) comb. nov. (Basionym: C. readii Stevenson, Kew Bull. 19: 9, 1964)

Spores elliptical or slightly subamygdaliform, hyaline, neither amyloid nor dextrinoid, smooth, 4-5 X 2-2.5 µ. Cystidia none. Cuticle a cutis consisting of repent, cylindrical, thin-walled, non. gelatinised hyphae, clamp connections present.

Hygrophorus muritaiensis Stevenson (28 D) = Camarophyllus muritaiensis (Stevenson) comb. nov. (Basionym: H. muritaiensis Stevenson, Kew Bull. 16: 378, 1962)
According to unpublished data of Horak and McNabb, this species seems to be a member of the genus Hygrophoropsis rather than anything else. Both genera are characterised by vein-like, forked gills but are clearly separated by distinct microchemical reactions of the spore wall.

Leucopaxillus waiporiensis Stevenson (29 D) Fig. 28 = Cantharellula waiporiensis (Stevenson) comb. nov. (Basionym: L. waiporiensis Stevenson, Kew Bull. 19: 19, 1964)

Spores subfusoid, amyloid, hyaline, smooth, 9.5-12 X 3.5-4.5 µ. Cystidia none. Cuticle a cutis consisting of regularly arranged, cylindrical, repent, clamp-bearing hyphae, encrusted with brownish pigment.

Hygrophorus elsae Stevenson (28 D) = Cantharellus elsae (Stevenson) comb. nov. (Basionym: H. elsae Stevenson, Kew Bull. 16: 375, 1962)

A redescription of this species will be published by McNabb in the near future.

This material (BERGGREN 138) undoubtedly belongs to Hygrophoropsis. The species was transferred to this genus by McNabb (1969).

Pleurotus cocciformis Berkeley (1 D, 16) = Chaetocalathus cocciformis (Berkeley) comb. nov. (Basionym: Agaricus (Pleurotus) cocciformis Berk. in Hook.f., Fl. Novae-Zelandiae 2: 174, 1855)

Despite the poor type material (New Zealand, Bay of Islands, 714) the taxonomic position of this species was finally resolved with the aid of additional collections. Our present knowledge indicates that this distinct species occurs exclusively on rotten wood of Vitex lucens.

Fig. 1 = Clitocybe albida (Stevenson) comb. nov. (Basionym: O. albida Stevenson, Kew Bull. 19: 12, 1964)

The spores are oval, smooth, neither amyloid nor dextrinoid, thin-walled, without germ-spore, 5-5.5 X 3-3.5 µ. Cystidia none. Cuticle consists of cylindrical, hyaline, nongelatinised hyphae, 3-6 µ. diam., with clamp-connections.

Fayodia grisella Stevenson and Taylor (29 D) Fig. 12 = Clitocybula grisella (Stevenson and Taylor) comb. nov. (Basionym: F. grisella Stevenson and Taylor, Kew Bull. 19: 47, 1964)

Spores oval to almost round, hyaline, amyloid, smooth, 5-6.5 X 4-5.5 µ (2-spored : 5.5-6 X 7 µ). Cheilocystidia present but not distinct. Caulocystidia club-shaped or somewhat irregular, thinwalled, distinctly coloured by a brown, plasmatic pigment. Cuticle of repent, cylindrical hyphae forming a cutis, with scattered club-shaped or fusoid, suberect dermatocystidia filled with a brown coloured cell sap, with clamp connections.

Several species belonging to the genus Collopus are represented in New Zealand, all of them closely related to the extremely variable C. epipterygius. Examined material: KIRK 20, BERGGREN 18; COLENso b 847.
Mycena subviscosa Stevenson (29 D) = Collopus subviscosus (Stevenson) comb. nov. (Basionym: M. subviscosa Stevenson, Kew Bull. 19: 55, 1964)

Marasmius drucei Stevenson (29 D) Fig. 7 = Collybia drucei (Stevenson) comb. nov. (Basionym: M. drucei Stevenson, Kew Bull. 19: 40, 1964)

Cuticle of interwoven, cylindrical, partially gelatinised hyphae with clamp connections. Spores comma-like, hyaline, neither amyloid nor dextrinoid, smooth, 7.5-9 X 3.5-4 µ. Cystidia none.

C. dryophila is a rather common species in the northern hemisphere, but was not found in New Zealand by us. However, Collybiopsis rimutaka (Stevenson) Horak which macroscopically resembles Collybia dryophila, was common throughout the country.

Marasmius kidsonii Stevenson (29 D) Fig. 14 Collybia kidsonii (Stevenson) comb. nov. (Basionym: M. kidsonii Stevenson, Kew Bull. 19. 40, 1964)

This species was originally found in lawns under Photinia, an introduced rosaceous plant. We are inclined to consider C. kidsonii an introduced fungus as well.

Fig. 14 = Naucoria sp. The preserved material (COLENSO b 760) is so badly damaged by insects that it is impossible to determine the structure of the cuticle or to find any cystidia. Spores slightly kidney-shaped, brownish in KOH, smooth, without germ pore, 8-9.5 X 4.5-5.5 µ. Because of the size and shape of the spores, we have no hesitation in placing this fungus in Naucoria. The genus is represented by several species in New Zealand's forests. The type of the taxon was redescribed by Pegler (1965) and belongs to Collybia.

Crinipellis novae-zelandiae Stevenson (29 D) Fig. 18 = Collybia novae-zelandiae (Stevenson) comb. nov. (Basionym: C. novae-zelandiae Stevenson, Kew Bull. 19: 45, 1964)

After careful study of the type material it is evident that this peculiar agaric is not correctly placed in Crinipellis. Although we twice collected this species, it is with some hesitation that we transfer this striking fungus to Collybia, and we anticipate that further changes will be made to its generic position.

Collybia nummularia (Fries) (8, 16) Fig. 19 = Pluteus sp.

The fragments of this collection (COLENSO b 741) are in poor condition but sufficient to confirm the identification. The spores are subglobose, smooth, pinkish, 7-8 X 5.5-7 µ.

Collybia radicata (Relhans) (6,16) Fig. 22 = Oudemansiella sp.

The spores of this collection (COLENSO b 356) are ± globose, hyaline to yellowish, neither amyloid nor dextrinoid, 9.5-13 µ diam. There are some similarities with the true European O. radicata, but unfortunately the poor state of the material prevents a comparison of all characters.

Crinipellis readii Stevenson (29 D) Fig. 23 = Collybia stevensonii Horak nom. nov. (non Collybia readii Stevenson, syn.)

Spores comma-like, hyaline, neither amyloid nor dextrinoid smooth, 7.5-9 X 3.5-4 µ. Cheilocystidia numerous, fusoid, with prolonged neck or irregularly branched apically, hyaline, 25-40 X 5-10 µ. Cheiocystidia cylindrical, thin-walled, densely covering the upper part of the stipe. Cuticle a cutis of irregularly interwoven cylindrical hyphae, encrusted with brown pigment, clamp connections present.

Collybia subclusilis Stevenson (29 D) Fig. 25 = Marasmius oreades (Fries) Earle

Spores almond-shaped to sublimoniform, hyaline, neither amyloid nor dextrinoid, smooth, 8-11.5 X 4.5-5.5 µ. This species was probably introduced with seeds (see habitat) and has to be regarded as a synonym of M. oreades.

Most mycologists would identify this material (COLENSO b 968) as conspecific with the true F. velutipes which grows throughout the northern hemisphere. From our observations we hesitate to consider F. velutipes as an introduced fungus in New Zealand and regard the New Zealand form as a distinct variety.

Crinipellis vinacea Stevenson (29 D) Fig. 27 = Collybia vinacea (Stevenson) comb. nov. Basionym: C. vinacea Stevenson, Kew Bull. 19: 44, 1964)

Spores elliptical, hyaline, neither amyloid nor dextrinoid, smooth, 7-8.5 X 3.5-4 µ. Cheilocystidia numerous, fusoid or ampullaceous, thin-walled, 25-40 X 5-9 µ. Cheiocystidia similar. Cuticle consisting of irregularly interwoven, cylindrical, externally pigmented hyphae, sometimes branched at the tips, without any dermatocystidia or hair-like elements, clamp connections present.

Marasmius cockaynei Stevenson (29 4) Fig. 4 = Collybiopsis cockaynei (Stevenson) comb. nov. (Basionym: M. cockaynei Stevenson, Kew Bull. 19: 39, 1964)

All microsopical characters clearly indicate that this fungus belongs to Collybiopsis. Cuticle of pileus consists of diverticulate cells, with clamp connections. The spores are elliptical or sligthly comma-like, hyaline, neither amyloid nor dextrinoid, smooth, 7.5-10 X 3-3.5 µ. Diverticulate cheilo- and caulocystidia present.

Marasmius kanukaneus Stevenson (29 D) = Collybiopsis kanukanea (Stevenson) comb. nov. (Basionym: M. kanukaneus Stevenson, Kew Bull. 19: 36, 1964)
Marasmius masonii Stevenson (29 D) Fig. 15 = Collybiopsis masonii (Stevenson) comb. nov. (Basionym: M. masonii Stevenson, Kew Bull. 19: 36, 1964)

Collybia rimutaka Stevenson (29 D) Fig. 23 = Collybiopsis rimutaka (Stevenson) comb. nov. (Basionym: C. rimutaka Stevenson, Kew Bull. 19: 8. 1964)

Spores 4.5-6.5 X 2.5-3 µ, neither amyloid nor dextrinoid, hyaline, smooth. Cuticle of irregular, broom-like cells, membranes encrusted with brown pigment, dextrinoid in Melzer's solution, clamp connections numerous. Cheilocystidia present. A very common species growing in all habitats in New Zealand.

Fig. 4 The type specimen (BERKELEY 5293) is well preserved. The spores of this small Coprinus, only 1-2 cm high, measure 7-8 X 3.5-4 µ and have a broad apical germ-pore. The globular cells of the veil (20-50 µ diam.) on top of the pileus are densely but minutely warted. These peculiarities put C. colensoi into sect. Vestiti (Lange) Kuhner and Romagnesi.
Apparently introduced into New Zealand with exotic grass seeds, soil, dung, etc.
There is a fungus growing on different kinds of rotten wood in New Zealand which in some respects looks like the above species. A study of the microscopical characters clearly showed that the New Zealand fungus is not conspecific with this northern hemisphere species. A full description will be published later.
The spores of this collection (SINCLAIR and HAAST 1860-61) measure 8.5-11 X 5.5-6.5 µ and are very similar in shape to those of European specimens. We suggest that C. fimetarius was accidentally introduced into New Zealand.
Crepidotus alveolus? Fries (6, 22 D) = Crepidotus novae-zelandiae Pilat (see there) Type material: COLENSO b 387.
Fig. 18 Examination of the type material (COLENSO b 387) confirmed Pilat's generic identification. Spores oval, brownish, thick-walled, smooth, without germ pore, 9.5-12 X 6.5-8 µ.

Crepidotus pezizoides Fries (6) Fig. 20 = Phialocybe sp.

Only spores (elliptical, minutely warted, 6-8 X 4-5 µ) could be identified from the fragments of the collection (COLENSO b 65). Unfortunately no other microscopical elements such as cheilocystidia, which are essential for correct indentification, could be found. More than half a dozen species of Phialocybe are known from New Zealand.

Crepidotus variabilis (Persoon) (6) Fig. 27 = Phialocybe sp.

Microscopical examination of this material (COLENSO b 385) revealed that this agaric is an undescribed species of Phialocybe. Unfortunately, its macroscopical characters are not fully known.

Because of the poorly preserved type material it was impossible to make a thorough examination of this species. Its systematic position remains doubtful therefore.
Crinipellis velutipes Stevenson (29 D) Doubtful species. Type material sterile.
The type collection has been lost (see Horak 1968:200), but we collected this species many times in the beech forests of New Zealand. Cuphocybe seems to be a good genus, endemic to New Zealand.
Cuphocybe olivacea Heim (24D) For discussion see C. alborosea Horak

Baeospora clastotricha Stevenson (29 D) Fig. 3 = Cystoderma clastotrichum (Stevenson) comb. nov. (Basionym: B. clastotricha Stevenson, Kew Bull. 19: 56, 1964).

This is undoubtedly a member of the genus Cystoderma which is represented in New Zealand by more than four species, according to our present knowledge. Cuticle consists of an epithelium formed by oval or roundish cells, with clamp, connections. Spores oval, hyaline, smooth, amyloid, 3.5-4.5 X 2.5-3 µ. Cystidia none.

Resupinatus dorotheae Stevenson (29 D) Fig. 7 = Delicatula dorotheae (Stevenson) comb. nov. (Basionym: R. dorotheae Stevenson, Kew Bull. 19: 23, 1964)

The almond-shaped spores (10.5-12 X 5.5-6 µ), structure of the cuticle, and habit of the fungus, place this species in Delicatula rather than Resupinatus.

Tricholoma hemisphaericum Stevenson (29 D) Fig. 13 = Dermoloma hemisphaericum (Stevenson) comb. nov. (Basionym: T. hemisphaericum Stevenson, Kew Bull. 19: 14, 1964)

Cuticle of smooth, thin-walled cells forming an hymeniderm, coloured with a brown, plasmatic pigment, clamp connections present. Spores oval, hyaline, amyloid, smooth, 5-6 X 3.5-4 µ. Cheilo- and pleurocystidia none.

Tricholoma murinum Taylor and Stevenson (29 D) Fig. 17 = Dermoloma murinum (Taylor and Stevenson) comb. nov. (Basionym: T. murinum Taylor and Stevenson, Kew Bull. 19: 17, 1964)

Cuticle cellular to hymeniform with epimembranous pigment encrusted cell walls, clamp connections present. Spores oval, hyaline, neither amyloid nor dextrinoid, smooth, 5.5-7 X 3.5-4 µ. Cystidia none.

Fig. 1 Spore size and shape in the preserved material (COLENSO b 1124) do not agree with those known for this species in Europe, but undoubtedly the fungus belongs to the genus Entoloma (Fr.) Kummer.
Entoloma botanicum Stevenson (27 D) = Entoloma nothofagi Stevenson (see there)
Entoloma citreostipitatum Stevenson (27 D) = Entoloma chloroxanthum Stevenson
Entoloma inconspicuum Stevenson (27 D) = Entoloma procerum Stevenson (see there)

Entoloma placidum (Fries) (11,16,27) Fig. 21 = Pluteus readii Stevenson

The examined material (COLENSO b 1204) agrees with this native Pluteus (see there) in all characters.

Entoloma pteridicola Stevenson (27 D) = Entoloma chloroxanthum Stevenson
Fig. 12 After studying the type material we found no evidence why this fungus should be placed in Fayodia and suggest that this species should be transferred to Mycena. It is very likely that this agaric is an introduced species since it grew in "fairy-rings" in a newly made lawn near Wellington.
Flammula brunnea Massee (16,D) Figs 2, 3 = Hypholoma brunneum (Massee) Reid 1955=. Type material: COLENSO b 668.
Flammula crociphylla Cooke and Massee (= Fl. xanthophylla C. & M.) (13 D, 11, 16)

Flammula fusa (Batsch) (6) Fig. 11 = Gymnopilus crociphyllus (Cooke and Massee) Pegler 1965.

In spite of the fully destroyed specimen (COLENSO b 243), we are quite convinced that the residual rust-brown, warted spores with a distinct, smooth plage (6-8 X 4-5 µ) are those of the above species. This Gymnopilus is one of the most common agarics in New Zealand.

The New Zealand collection (COLENSO b 821) belongs to the genus Gymnopilus. It is clearly not conspecific with the type collection (from Australia) which is currently called Phylloporus hyperion (Cooke and Massee) Singer.
Fig. 20 Under this name four collections can be found at Kew: the material labelled (COLENSO b 70) belongs to an undescribed species of Gymnopilus which grows mainly on rotten wood of Leptospermum. The other three collections (COLENSO b 51, b 210, b 311) represent Gymnopilus crociphyllus (Cooke and Massee) Pegler. Spores oval, with distinct smooth plage, otherwise warted, rust-brown, 5-6 X 3.5-4 µ.

Flammula purpureonitens Cooke and Massee (11,16)

Pegler (1965) examined the type which was collected in Australia and transferred the species to Gymnopilus. We are inclined to put it in Cortinarius.

Flammulina glutinosa Stevenson (29 D) Fig. 11 = Mycena leiana (Berkeley) Saccardo.

This is a unique, glutinous, deep orange coloured Mycena known only from North America. We compared the New Zealand specimen with material collected in the U.S. and did not find a single character separating the two. It may well be that M. leiana was accidentally introduced into New Zealand and should therefore be tentatively included in the list of the adventitious fungi.

Mycena miniata Stevenson (29 D) = Galactopus miniatus (Stevenson) comb. nov. (Basionym: M. miniata Stevenson, Kew Bull. 19: 54, 1964)

Mycena morris-jonesii Stevenson (29 D) Figs 16, 17 = Galactopus morris-jonesii (Stevenson) comb. nov. (Basionym: M. morris-jonesii Stevenson, Kew Bull. 19: 52, 1964)

Spores oval, hyaline, amyloid, smooth, 7.5-9 X 4.5-6 µ. Cheilo- and pleurocystidia fusoid or awl-shaped, thin-walled, coloured with a reddish plasmatic pigment, 50-70 X 10-15 µ.

Mycena parsonsii Stevenson (29 D) = Galactopus parsonsii (Stevenson) comb. nov. (Basionym: M. parsonsii Stevenson, Kew Bull. 19: 56, 1964)

Galera tenera (Fries) (8,16) Fig. 26 = Psilocybe sp.

The material (BERGGREN 60) consists of badly preserved carpophores possessing large spores 18-20 X 10-11 µ, with a smooth brown wall and prominent germ pore. According to the scanty data this species belongs to Psilocybe, rather than Galerina or Conocybe.

Unfortunately no material of this species exists, but it is very likely that the agaric described under this name is conspecific with an annulate Galerina which grows everywhere in New Zealand.
Hygrophorus gloriae Stevenson (28 D) = Gliophorus gloriae (Stevenson) comb. nov. (Basionym: H. gloriae Stevenson, Kew Bull. 16: 382, 1962)
Hygrophorus viridis Stevenson (28 D) = Gliophorus viridis (Stevenson) comb. nov. (Basionym: H. viridis Stevenson, Kew Bull. 16: 383, 1962)

Hebeloma strophosum (Fries) Fig. 25 = Agrocybe sp.

The characters of a collection under this name at Kew ("New Zealand") indicate that this material is not a Hebeloma. Because of the still visible ring and smooth spores with a broad germ pore, this fungus is placed in Agrocybe. In the absence of data on the colour and other ephemeral characters of fresh carpophores, a reliable identification cannot be made.

Panellus atrofulvus Stevenson (29 D) Fig. 2 = Heimiomyces atrofulvus (Stevenson) comb. nov. (Basionym: P. atrofulvus Stevenson, Kew Bull. 19: 29, 1964)

Spores cylindric to slightly phaseoliform, hyaline, amyloid, thin-walled, without germ-pore, 7.5-10.5 X 3.5-4.5 µ. Cheilocystidia none. Caulocystidia irregularly branched, diverticulate, thick-walled, membrane coloured with brown pigment, weak reaction in Melzer's solution, clamp connections present.

Tectella luteohinnulea Stevenson (29 D) Fig. 15 = Hohenbuehelia luteohinnulea (Stevenson) comb. nov. (Basionym: T. luteohinnulea Stevenson, Kew Bull. 19: 30, 1964)

There is no reason why this species should have been described in Tectella, especially seeing that the "veil", which is specific to Tectella, is apparently formed by the remnants of a web-like cover produced by insects.

Panellus metuloideus Stevenson (29 D) Fig. 16 = Hohenbuehelia metuloidea (Stevenson) comb. nov. (Basionym: P. metuloideus Stevenson, Kew Bull. 19: 27, 1964)

A glance at the illustrations shows that this species clearly has to be transferred to Hohenbuehelia.

Hohenbuehelia parsonsii Stevenson (29 D) = Hohenbuehelia petaloides (Fries) Schulzer

This species may be introduced as it is frequently found on ruderal places or in lawns.

Hohenbuehelia tristis Stevenson (29 D) = Hohenbuehelia nothofaginea Stevenson
Hygrophorus fuscoaurantiacus Stevenson (28 D) = Hygrocybe fuscoaurantiaca (Stevenson) comb. nov. (Basionym: H. fuscoaurantiacus Stevenson, Kew Bull. 16: 381, 1962.)
Hygrophorus julietae Stevenson (28 D) = Hygrocybe julietae (Stevenson) comb. nov. (Basionym: H. julietae Stevenson, Kew Bull. 16: 377, 1962)
Hygrophorus keithgeorgii Stevenson (28 D) = Hygrocybe keithgeorgii (Stevenson) comb. nov. (Basionym: H. keithgeorgii Stevenson, Kew Bull. 16: 378, 1962)
Hygrophorus lilaceo-lamellatus Stevenson (28 D) = Hygrocybe lilaceo-lamellatus (Stevenson) comb. nov. (Basionym: H. lilaceo-lamellatus Stevenson, Kew Bull. 16: 378, 1962)
Hygrophorus mavis Stevenson (28 D) = Hygrocybe mavis (Stevenson) comb. nov. (Basionym: H. mavis Stevenson, Kew Bull. 16: 377, 1962)
Hygrophorus procerus Stevenson (28 D) = Hygrocybe procera (Stevenson) comb. nov. (Basionym: H. procerus Stevenson, Kew Bull. 16: 380, 1962)
Hygrophorus rubrocarnosus Stevenson (28 D) = Hygrocybe rubrocarnosa (Stevenson) comb. nov. (Basionym: H. rubrocarnosus Stevenson, Kew Bull. 16: 379, 1962)
The poor state of the exsiccaturn (N.Z., Dr Berggren) did not allow detailed observations, but there is no doubt that this species belongs to Hygrophorus, as already stated by Stevenson (28).
This doubtful species was described in Cantharellus by Cleland although he commented that it was probably better placed in Omphalia. Type material has not been studied.
Probably introduced into New Zealand, growing mainly on lawns around houses and in parks. This species, however, is closely related to an undescribed native fungus.

Hygrophorus cyaneus Berkeley (3 D, 4, 16, 27) = Entoloma hochstetteri (Reichardt) Stevenson

No specimens have been preserved but a well executed painting of this distinctive fungus by J. V. Haast exists at Kew. For further details see Stevenson (27).

Hygrophorus miniceps Stevenson (28 D) = Hygrocybe procera (Stevenson) Horak; for discussion see there.
Stevenson's description of this species is based on two different collections which we also have studied. Not only are the spore dimensions of the two collections widely different but we believe that neither of them can be identified with H. multicolor.

213. X ? Hygrophorus niveus Fries (8)

It is quite likely that this record represents Hygrocybe mavis (Stevenson) Horak, which macroscopically resembles H. niveus.

Hygrophorus variabilis Stevenson (28 D) = Cantharellus sp.
The systematic position of this species remains doubtful because there are several characters such as structure of the cuticle and the cheilo- and caulocystidia which indicate that it is near Hydropus or Gerronema.

Omphalina roseola Stevenson (29 D) Fig. 24 = Hygrotrama roseolum (Stevenson) comb. nov. (Basionym: O. roseola Stevenson, Kew Bull. 19: 12, 1964)

Spores, oval to subglobose, hyaline, neither amyloid nor dextrinoid, smooth, 5.5-6.5 X 4-5 µ. Cheilocystidia club-shaped, thin-walled, non-pigmented, 20-45 X 8-17 µ. Cuticle hymeniform, consisting of club-shaped, thin-walled cells, encrusted with epimembranous pigment, clamp connections none.

Examination of the well preserved type collection (COLENSO b 48) shows that this distinct species belongs to Hypholoma (Fr.) Kummer and accordingly the combination Hypholoma acutum (Cooke) comb. nov. is proposed.
(Basionym: Agaricus (Naucoria) acutus Cooke, Grevillea 14: 129, 1886)

Hypholoma fasciculare (Fries) (1, 16) Fig. 9 = Hypholoma acutum (Cooke) Horak

All characters of this collection (COLENSO b 408) correspond well with the type of H. acutum, a very common species in the forests of New Zealand.

The type material (COLENSO 1264) is not only mouldy, but also has been attacked by insects, so that it was not possible to examine any microscopical structures. Under these circumstances the systematic position of this species cannot be resolved.
Mycena roseoflava Stevenson (29 D) = Insitica roseoflava (Stevenson) comb. nov. (Basionym: M. roseoflava Stevenson, Kew Bull. 19: 50, 1964)
The New Zealand collection of this species (COLENSO b 706) does not differ very much from the type collected in Brisbane, Australia. For further information see Pegler (1965).
All species of this genus occurring in New Zealand are being studied by McNabb.
Fig. 13 The spores of the type (native to Tasmania) are slightly smaller than those of the New Zealand collection (COLENos b 969). Unfortunately the poor state of the material makes it impossible to compare this fungus with one of the numerous species of Hemicybe in New Zealand.
Unfortunately, in the absence of any material, it cannot be proved whether the identification was correct. However, we found on several occasions a species which showed some similarities to the true L. clypeolaria from Europe, and it may well be that the New Zealand material represented this species.
Fig. 9 Despite the poor state of the material (SINCLAIR, Auckland 26.IV.1854) microscopical characters and collection notes justify placing this species in Macrolepiota. The spores are typical of this genus: thick-walled, slightly dextrinoid, with distinct germ-pore, 13-16 X 9-10.5 µ. We suppose that this species was accidentally introduced into New Zealand.
Figs. 16, 17 Two collections under this name (COLENSO b 840, b 881) are still in existence but they differ distinctly from each other. More details will be given in a study of Lepiota to be published later.

Pluteus purpuratus Stevenson (26D) Fig. 22 = Lepiotula purpurata (Stevenson) comb. nov. (Basionym: P. purpuratus Stevenson, Kew Bull. 16: 73, 1962)

Spores dextrinoid, indistinctly spurred, smooth, germ pore none, 5.5-6 X 3.5-4 µ. Cheilo- and pleurocystidia not observed (type material in fragmentary condition). The dimensions of the spores given by Stevenson are based on measurements of alien Psathyrella spores. The free gills were obviously the reason for assigning the fungus to Pluteus.

No type collection was found in Kew. Another collection under the same name (STEV. 1097) proved to be a species of Rhodocybe Maire.
A thorough study of the type and several collections made by ourselves clearly showed that this species is taxonomically unrelated to Leucopaxillus. Details of its systematic position will be published in a later paper.

Leucopaxillus otagoensis Stevenson (29 D) Fig. 20 = Clitocybe clitocyboides (Cooke and Massee) Pegler, 1965

It is difficult to see why this fungus was originally described in Leucopaxillus for apart from the decurrent gills, it has nothing in common with that genus. C. clitocyboides closely resembles C. hydrogramma (Fries) Singer even to the distinct chlamydospores embedded between hyphae of the cuticle. All characters of the N.Z. species correspond well with those of the type from Australia.

We observed a single fruiting body of this introduced species under pines among the dunes near Collingwood.
This species belongs to a group of apparently related Marasmiellus-like fungi known from New Zealand which possess subamygdaliform, smooth spores and long, thick-walled, yellow-brown, hair-like dermatocystidia in the cuticle. To our knowledge there is no existing genus where these fungi could be adequately accommodated.

Resupinatus tristis Stevenson (29 D) Fig. 26 = Marasmiellus tristis (Stevenson) comb. nov. (Basionym: R. tristis Stevenson, Kew Bull. 19: 23, 1964)

Spores almond-shape, hyaline, neither amyloid nor dextrinoid, smooth, 8-10 X 5-6 µ. Cheilocystidia broom-like or diverticulate. Cuticle consisting of diverticulate cells, clamp connections present.

Resupinatus violaceo-griseus Stevenson (29D) Fig. 28 = Marasmiellus violaceo-griseus (Stevenson) comb. nov. (Basionym: R. violaceo-griseus Stevenson, Kew Bull. 19: 22, 1964)

Spores elliptical to subcylindrical, hyaline, neither amyloid nor dextrinoid, smooth, 5-6.5 X 2.5-3 µ. Cheilocystidia broom-like. Cuticle of heavily diverticulate cells, clamp connections present.

Lentinus delicatus Stevenson (29 D) Fig. 6 = Marasmius delicatus (Stevenson) comb. nov. (Basionym: L. delicatus Stevenson, Kew Bull. 19: 32, 1964)

Cuticle of hymeniform cells, walls smooth, not broom-like, clamp connections present. Spores 8-10 X 3-3.5 µ, comma-like to fusoid, hyaline, smooth, neither amyloid nor dextrinoid. Cheilo- and caulocystidia present.

Fig. 8 The specimen preserved under this name (KIRK 23) belongs in Galerina. Spores 7.5-9 X 4-5 µ almond-shaped, warty, with a distinct, smooth plage. Pleurocystida 45-60 X 14-20 µ, lageniform, thin-walled, hyaline, with clamp connection at basal septum.
The systematic position of the fungi in this collection (COLENSO b 1008) is unresolved. Macroscopically the carpophores resemble the type material from Australia (Brisbane, F. M. Bailey, Nr. 26, in K; see also Pegler, 1965), but the tiny (4-5 X 2-3 µ), neither amyloid nor dextrinoid, smooth spores clearly separate the two taxa.
Fig. 13 The type collection (COLENSO b 563) consists of fruiting bodies up to 1 cm in diam. with an often excentrically inserted stipe, growing on rotten wood. Spores slightly amygdaliform or comma-like, neither amyloid nor dextrinoid, smooth, 7.5-9.5 X 4-5 µ. According to our knowledge M. inversus is a good species of Marasmius sensu lato.
Stevenson may well have been right in placing this species in Crinipellis, but a final decision cannot be made without type material or new collections from the neighbourhood of the type locality (Auckland).
We have observed this fungus several times. It has obviously been introduced with seeds, straw or other media. See Collybia subclusilis Stevenson (no. 308).
Marasmius tinctorius Massee (15 D) Fig. 26 = Hypholoma acutum (Cooke) Horak

Tricholomopsis vinosa Stevenson (29 D) Fig. 27 = Melanoleuca vinosa (Stevenson) comb. nov. (Basionym: T. vinosa Stevenson, Kew Bull. 19: 7, 1964)

Spores oval, hyaline, weakly amyloid, minutely warted, no distinct plage, 5-6 X 3-3.5 µ. Cheilocystidia none. Pleurocystidia fusoid, apically encrusted with crystals, 30-40 X 4-6 µ. Cuticle of irregularly arranged short-celled hyphae, thin-walled, covered with brown epimembranous pigment. All hyphae bear clamp connections.

If correctly indentified, this species must be regarded as an introduced fungus in New Zealand.
The spores of the two collections studied (COLENSO 1005, b 412) are quite similar to those of European specimens of this species. The tiny carpophores made it difficult to study the structure of the cuticle and other characters essential for an exact identification.

Mycena conicola Stevenson (29 D) Fig. 4 = Mycena aff. flos-nivium Kuhner

The type is poorly preserved but nevertheless several important details were obtained. According to these characters this fungus approaches M. flos-nivium which grows in Europe on rotten cones os spruce from late winter until spring. The New Zealand material was collected at the end of June, on cones of spruce. The structure of the cuticle and size and shape of the cheilocystidia and spores (110.-12 X 4.5-5 µ) support this identification. It is recommended that M. conicola be regarded as a synonym of M. flos-nivium and added to the list of exotic fungi in New Zealand.

Probably introduced into New Zealand, growing mainly on lawns around houses and in parks. This species, however, is closely related to an undescribed native fungus.

Fayodia cystidiosa Stevenson (29 D) Fig. 6 = Mycena cystidiosa (Stevenson) comb. nov. (Basionym: F. cystidiosa Stevenson, Kew Bull. 19: 46, 1964)

This is a very peculiar species of the genus Mycena. The conspicuous cheilo- and pleurocystidia are apically ornamented with irregular thick-walled, hyaline excrescences. Spores 8.5-12 -X 6-7.5 µ, oval, hyaline, weakly amyloid, smooth.

It was impossible to obtain reliable data from this poorly preserved collection (BERGGREN 16).
The size of carpophores, and spores of this collection (COLENSO b 228) clearly differ from those of true M. galericulata known from the northern hemisphere.
From the poor type material we recovered a few spores which correspond fairly well with the data and observations given by Stevenson. As the structure of the cuticle could not be studied the taxonomic position of this species must remain doubtful.
After studying the fragmentary remains of this collection (COLENSO b 89) we can confirm only that this fungus is not conspecific with typical M. lactea. The only character in common seems to be the white colour of the carpophores.

Mycena mariae Stevenson (29 D) Fig. 15 = Galactopus morris-jonesii (Stevenson) Horak

Spores oval, hyaline, amyloid, smooth, 8-11.5 X 5-6 µ. Cheilo- and pleurocystidia fusoid or awl-shaped, thin-walled, filled with a reddish cell sap, 55-75 X 10-16 µ.

Mycena multicolorata Stevenson (29 D) = Insiticia flavovirens (Cooke and Massee) Horak. I. flavovirens was originally described from Australia, where it was found growing on trunks of tree ferns imported from New Zealand. We checked the type material of both species which is clearly conspecific (see Pegler, 1965) and in addition collected this agaric on two occasions on its rather specialised host substratum.

Fayodia ochracea Stevenson (29 D) Fig. 19 = Mycena ochracea (Stevenson) comb. nov. (Basionym: M. ochracea Stevenson, Kew Bull. 19: 47, 1964)

Spores oval to elliptical, hyaline, weakly amyloid, smooth, 8.5-10.5 X 5-6 µ. Cheilocystidia numerous, fusoid, irregularly branched or broom-like, hyaline, thin-walled, 25-50 X 5-10 µ. Possibly introduced.

The poor state of the type collection precludes an accurate examination of the microscopical characters of this species. Because of this, it is uncertain whether M. pinicola is an introduced species. The fungus was found growing in litter in Pinus plantations.
The preserved material (COLENSO b 264) consists of a mixed collection; one part belongs to Naucoria (fig. 252 a) and the other represents a species of Oudemansiella (fig. 252 b) closely related to or identical with a fungus called Ag. (Collybia) radicata (Fries) (COLENSO b 356; see there).
Mycena primulina Stevenson (29 D) Fig. 21 Spores oval, hyaline, inamyloid, smooth, 4-5 X 3 µ. Cystidia fusoid to awl-shaped, hyaline, 20-32 X 4-7 µ.
255 Mycena primulina: a. spores.
Mycena fuscovinacea Stevenson (29 D) = Mycenula fuscovinacea (Stevenson) comb. nov. (Basionym : M. fuscovinacea Stevenson, Kew Bull. 19: 53, 1964)

Naucoria aurora Cooke and Massee (7 D) Fig. 2 = Hydrocybe sp.

The type material (Bergren 134) is in poor condition, but according to the spores which are rust-coloured, minutely warty, ellipsoid, 6.5-8 X 4.5µ, this species must be considered an Hydrocybe. Cystidia absent.

Fig. 3 This species (COLENSO b 360) is very closely related to or even conspecific with an undescribed species of Gymnopilus collected by us in New Zealand on several occasions.
Fig. 8 The examination of the collection (COLENSO b 319) showed that in all characters it is typical of Pholiota, sect. Pholiota. More details about this remarkable species will be published later.
Fig. 10 The microscopical characters of this collection (COLENSO b 500) in some respects resemble those of Hypholoma acutum (Cooke) Horak, but the material is not sufficiently well preserved to allow positive identification. It should be mentioned that the type of N. fraterna comes from Australia. The species was transferred to Laccaria by Pegler (1965).
Fig. 11 The microscopical characters of this collection (BERGGREN 142) show some affinities to those of a distinct secotiaceous genus as yet unpublished, endemic to New Zealand. To my knowledge, this taxon is distributed throughout the forests of New Zealand.

Naucoria nasuta (Kalchbrenner) (8,16) Fig. 18 = Galerina sp.

This collection (COLENSO 1039) corresponds in all characters with the material described in this list under No. 177. Spores almond-shaped, distinctly warted, with smooth plage, brown, 8-9.5 X 4.5-5 µ, sometimes with visible germ pore. Pleurocystidia fusoid, apically bifurcate, thin-walled, non-pigmented, with clamp connection, 45-60 X 12-18 µ.

Naucoria pediades (Fries) (6,16) Fig. 20 = Agrocybe pediades (Fries) Fayod

All characters of the N.Z. collection (COLENSO 269) are similar to those of this fungus in Europe. Probably another introduced fungus growing by preference in paddocks and lawns.

293. X A Naucoria semiorbicularis (Fries) (4,8,16) = Agrocybe semiorbicularis (Fries) Fayod

Although the material (BERGGREN 61) is half destroyed by insects all the diagnostic microscopical characters of this European species were found. It is apparently an introduced fungus in New Zealand.

The spores of this collection (COLENso b 751) are yellowish-grey, smooth, 8-10 X 5-6 I,. Cheilocystidia broom-like or diverticulate. kidney-shaped, 6.5-7.5 X 3.5-4 µ. No cystidia seen. These characters are insufficient to determine the systematic position of this collection.

Omphalia ? anthiceps Berkeley and Curtis (8, 16) Fig. 2 = Cystoderma clastotrichum (Stevenson) Horak

The microscopical as well as macroscopical characters of the collection (COLENSO b 1023) correspond in all details with this common New Zealand species of Cystoderma, which was originally described as Baeospora clastotricha Stevenson (see there).

The poorly preserved type (COLENSO 440-217b) made it impossible to find any details necessary for an exact classification.

Omphalia epichysium (Persoon) (6) Fig. 7 = Xeromphalina racemosa Stevenson

The original collection (COLENSO b 138, on logs in woods) is well preserved and there are no problems in identifying the specimen. The spores are strongly amyloid, oval, smooth, 4.5-5.5 X 4-4.5(5) µ and only slightly smaller than those of the type.

The lack of cystidia and the size of the spores (7-8 X 3.5-4.5 µ) exclude the probability that this specimen (KIRK 233) is conspecific with typical O. fibula.
Omphalia leonina Massee (16 D) Fig. 14 = Xeromphalina racemosa Stevenson and Taylor. This species was collected by Massee in Kew Gardens on a mossy piece of wood imported from New Zealand. All micro- and macroscopical characters correspond with X. racemosa which grows in New Zealand preferably on rotten wood of Nothofagus. Spores oval, hyaline, amyloid, smooth, 5-6 X 3.5-4.5 µ.

Omphalia stellata (Fries) (8,16) Fig. 25 = Mycena veronicae Stevenson

The identification of this material (COLENSO 545 b) is confirmed by the typical club-shaped cells in the cuticle filled with a brown cell sap, decurrent gills, and the ovoid spores.

There are two collections (COLENSO b 737, KIRK 71) at Kew referred to O. umbellifera, but the microscopical characters of both do not agree with those of this common European species.
 

Cantharellula foetida Stevenson (29 D) Fig. 10 = Omphalina foetida (Stevenson) comb. nov. (Basionym: C. foetida Stevenson, Kew Bull. 19: 18, 1964).

Cuticle of repent, cylindrical, interwoven hyphae forming a cubs, with epimembranous pigment, clamp connections none. Spores oval, hyaline, neither amyloid nor dextrinoid, smooth, 5.5-7 X 5 µ,. Cystidia none.

Clitocybe nothofaginea Stevenson (29 D) Fig. 18 = Omphalina nothofaginea (Stevenson) comb. nov. (Basionym: C. nothofaginea Stevenson, Kew Bull. 19: 5, 1964)

Cuticle consisting of cylindrical, non-gelatinised, clampless hyphae forming a cutis, with epimembranous pigment. Spores oval, hyaline, neither amyloid nor dextrinoid, smooth, 5-6 X 3-4 µ. Cystidia none.

Omphalina sulphurea Stevenson (29 D) = aff. Hygrophorus sp.
Examination of the type material and of additional fresh carpophores showed clearly that this rather common species in New Zealand does not belong in Omphalina. The specific characters indicate a distinct relationship to Gerronema sensu. Singer. More studies are necessary to extend our knowledge of this peculiar agaric.

Limacella macrospora Stevenson (26 D) = Oudemansiella macrospora (Stevenson) comb. nov. (Basionym: L. macrospora Stevenson, Kew Bull. 16: 68, 1962)

A full description of this species will be published later.

Panellus cremeus Stevenson (29 D) Fig. 5 = Pleurotopsis subgrisea (Stevenson) Horak.
Panellus fulgens Stevenson (29D) Fig. 10 = Pleurotopsis subgrisea (Stevenson) Horak (see there)

Panellus niger Stevenson (29 D) Fig. 10 = Hydropus sp.

Spores oval to elliptical, hyaline, weakly amyloid, smooth, 4-4.5 X 2-2.5 µ. Cystidia none. Cuticle with intermixed oleiferous hyphae showing in KOH a dark brown plasmatic pigment, with clamp connections.

264. + Panus purpuratus Stevenson (29 D)

Fig. 22 Spores allantoid, hyaline, neither amyloid nor dextrinoid, smooth, 5-6 X 1.5-2 µ. Cheilo- and pleurocystidia fusoid, thin-walled, without crystals, coloured with a yellow plasmatic pigment, 40-90 X 8-11 µ. Cuticle consisting of suberect fusoid or cylindrical cells forming a loose trichoderm, membrane of the hyphae not gelainised, with clamp connections.

This collection (COLENSO 798) is represented by several carpophores which have been badly eaten by insects. Spores none, systematic position uncertain.
Phaeomycena fusca Stevenson and Taylor = Pluteus sp., there are no doubts about the taxonomic position of this collection and we see no reason to place it in the monotypic genus Phaeomycena which was recorded once from Madagascar.
Fig. 1 Microscopical characteristics of the preserved material (COLENSO 368) agree closely with those of Pholiota aurivella (Fr.) Kummer. I am inclined to regard this fungus as an adventitious species.
Fig. 7 A well developed annulus can still be observed on the carpophores of this collection (N.Z.), but the spores are definitely different from those of Agrocybe erebia. They have an obvious germ-pore, are thick-walled and measure 8.5-10 X 5.5-6.5 µ.

Hypholoma glutinosum Massee (15 D) Fig. 12 = Pholiota glutinosa (Massee) comb. nov. (Basionym: H. glutinosum Massee, Kew Bull. 1898: 132, 1898)

Spores oval, brown, smooth, with broad and distinct germ-pore, 7.5-10 X 4-5.5 µ. Chrysocystidia fusoid, with a deep yellow-brown, plasmatic pigment in KOH, 40-60 X 9-14 µ.

No spores were found in the material examined (COLENso b 242)
Pholiota praecox (Fries) (6) = Agrocybe praecox (Fries) Fayod The collection (COLENSO b 283) contains a single, immature carpophore but all found characters correspond well with those of the type. It has probably been introduced from overseas.

Pholiota squarrosa (Fries) (12,16) = Gymnopilus sp.

From the preserved material (COLENSO 3850 B) referred to this species, only a few spores have been observed. These spores are distinctly warty, rust-brown, show a distinct plage, and are characteristic of Gymnopilus rather than any other genus.

The microscopical characters of this material (BERGGREN 70) indicate that this fungus is identical with a widely distributed species of Galerina which grows mainly on rotten wood of Nothofagus cliffortioides.

Lentinellus cremeus Stevenson (29 D) Fig. 5 = Pleurocollybia cremea (Stevenson) comb. nov. (Basionym: L. cremeus Stevenson, Kew Bull. 19: 21, 1964)

It is difficult to comprehend why Stevenson placed this fungus, which is common in the New Zealand bush, in Lentinellus. All characters indicate an obvious relationship with Pleurocollybia, a genus not previously known from New Zealand. Spores roundish, hyaline, weakly amyloid, smooth, 2.5-3 X 2.5 µ.

Panellus roseolus Stevenson (29 D) Fig. 24 = Pleurotopsis roseola (Stevenson) comb. nov. (Basionym: P. roseolus Stevenson, Kew Bull. 19: 28, 1964)

Spores cylindrical or slightly allantoid, amyloid, smooth, 6.5-7 X 2.5-3.5 µ. Cheilocystidia none. Cuticle a thick layer of strongly gelatinised hyphae forming a cutis, clamp connections present.

Panellus subgriseus Stevenson (29 D) Fig. 26 = Pleurotopsis subgrisea (Stevenson) comb. nov. (Basionym: P. subgriseus Stevenson, Kew Bull. 19: 27, 1964)

Spores slightly allantoid to cylindrical, amyloid, hyaline, smooth, 7.5-10 X 3-4 µ. Cystidia none. Cuticle a cutis consisting of a thick layer of strongly gelatinised, cylindrical hyphae, clamp connections present.

The N.Z. material (COLENSO 395) is poorly preserved in every respect and it was impossible to find spores. The type collection was described from Tasmania (growing on Eucalyptus amygdalina) and represents a species of Pleurotus (Pegler 1965:323).

Fig. 2 = Hohenbuehelia aff. nothofaginea Stevenson

The size and dimensions of the microscopical characters found in this collection (COLENSO 1007) are very similar to those of H. nothofaginea Stevenson.

In spite of sterile fruiting bodies (N.Z., 1866, 6282) there is no doubt that this collection belongs to Resupinatus, a genus represented in N.Z. by at least two species.
Of the three collections in Kew, one belongs to Henzicybe Karsten (COLENSO b 534), while the two remaining collections (COLENSO b 329, b 975) are conspecific with Hohenbuehelia nothofaginea Stevenson.

Pleurotus bursaeformis (Berkeley) (11,16) = Hohenbuehelia bursaeformis (Berkeley) Reid, Kew Bull. 17: 304, 1963.

A detailed study of this polymorphic species which is widely distributed throughout the Pacific basin, will be published at a later date.

The preserved collection (COLENSO b 106) consists of some small stipitate carpophores possessing comma-like spores about 7-9.5 X 3-3.5 µ. The taxonomic position of this species cannot be clarified until further collections have been made.
Pleurotus colensoi Berkeley apud Massee (16 D) = Hohenbuehelia bursaeformis (Berkeley) Reid (see there).

Pleurotus euphyllus Berkeley (9 D) = Hohenbuehelia bursaeformis (Berkeley) Reid. Type material: SINCLAIR 1860.

This is another synonym of the common New Zealand species H. bursaeformis (see there).

Fig. 10 The New Zealand collection (COLENSO b 652) differs in several features from the type (fig. 112 b), originally described from Ceylon. The most striking difference is in spore size: 6.5-8.5 X 3-3.5 µ (type), 8.5-11.5 X 4-4.5 µ (N.Z. specimen).

131. X ? Pleurotus guilfoylei Berkeley (8, 16)

There is no material from New Zealand, but examination of the type revealed the fact that Pl. guilfoylei must be considered a further synonym of Hohenbuehelia bursaeformis (Berkeley) Reid (see also Pegler, 1965).

Pleurotus salignus (Persoon) (8,16) Fig. 24 = Pleurotus sp.

The cylindrical spores of this collection (COLENSO b 876) are distinctly smaller (7-9 X 3-3.5 µ) than those of typical P. salignus. At the same time all characters of this species differ from those of other Pleurotus species hitherto found in New Zealand.

According to Pegler (1965) the type of this species seems to be a well characterised species of the genus Pleurotus. The New Zealand material, however, is totally different. One collection (COLENSO b 973) represents a species of Scytinotus Karsten (see fig. 290 a), with allantoid spores, measuring about 6-7 X 2.5-3 µ. In the other collection (COLENSO 749) we found elliptical spores with a brownish, minutely warted membrane, 7-9 X 3-3.5 µ (see fig. 290 b), it being a Phialocybe Karsten.

Pleurotus serotinus (Fries) (6) Fig. 25 = Hohenbuehelia nothofaginea Stevenson

After studying this collection (COLENSO b 72) we cannot see any differences between it and H. nothofaginea, a ubiquous fungus in the beech forests of New Zealand.

Pleurotus sordulentus Berkeley and Broome (11,16,29) = Hohenbuehelia brusaeformis (Berkeley) Reid. Examined material: COLENSO b 1230

Pleurotus tasmanicus Berkeley (8,16) = Hohenbuehelia bursaeformis (Berkeley) Reid.

Because of the subglobose, spiny or warted spores and the short, fusoid and slightly thick-walled pleurocystidia this collection (COLENSO b 896) can be identified as H. bursaeformis. This collection has nothing in common with the type from Tasmania which is considered to be a synonym of Panellus diversipes (Berkeley) Pegler 1965.

Pluteus muscicola Stevenson (26 D) Fig. 17 = Pluteolus muscicola (Stevenson) comb. nov. (Basionym: P. muscicola Stevenson, Kew Bull. 16: 72, 1962)

Spores elliptic, rust: brown to ochraceous, smooth, with broad apical germ pore, 8-11 X 4.5-5.5 µ. Cuticle of articulate cells forming an hymeniderm, with brown plasmatic pigment, clamp connections none.

The examination of this collection (COLENSO B 353) showed that this agaric is conspecific with a very common species of Pluteus in New Zealand which is closely related to the European P. atricapillus (Secretan) Singer.

Tricholoma amyloideum Stevenson (29 D) = Porpoloma amyloideum (Stevenson) comb. nov. (Basionym: T. amyloideum Stevenson, Kew Bull. 19: 15, 1964)

This is the first record of the South American genus Porpoloma in New Zealand.

Cantharellula fistulosa Stevenson (29 D) = Pseudoarmillariella fistulosa (Stevenson) comb. nov. (Basionym: C. fistulosa Stevenson, Kew Bull. 19: 18, 1964)

Spores oval, hyaline, amyloid, smooth, 5-6 X 3.5-4 µ; cheilocystidia club-shaped, thin-walled, 20-55 X 10-18 µ with clamp connection at the basal septum; cuticle of interwoven, cylindrical hyphae, forming a cutis, with scattered dermatocystidia-like cells.

The identification of Stevenson cannot be confirmed because carpophores of the type material are sterile.
Resupinatus purpureo-olivaceus Stevenson (29 D) = Anthracophyllum sp.

Fig. 2 = Rhodocybe albovelutina (Stevenson) comb. nov. (Basionym: L. albovelutinus Stevenson, Kew Bull. 19: 32, 1964)

There is no doubt that this species with pinkish, angular spores, 5.5-7 X 3.5-5 µ, has to be transferred to Rhodocybe.

Lepista muritai Stevenson (29 D) Fig. 17 = Rhodocybe muritai (Stevenson) comb. nov. (Basionym: L. muritai Stevenson, Kew Bull. 19: 7, 1964)

Cuticle consisting of cylindrical, not gelatinised, clamp connection-bearing hyphae, forming a cutis, interwoven with oleiferous vessels. Spores rough to minutely corrugated-angular, pinkish, oval, 6-7.5 X 3.5-4 µ. Cystidia none.

Lepista piperata Stevenson (29 D) Fig. 21 = Rhodocybe piperata (Stevenson) comb. nov. (Basionym: L. piperata Stevenson, Kew Bull. 19: 6, 1964)

Spores oval to elliptical, pinkish, rough, 7-10 X 5-6 µ. Cystidia none. Cuticle a cutis consisting of cylindrical, interwoven, thin-walled, clampless hyphae.

Quite common throughout the country.

Stropharia lepiotaeformis Cooke and Massee (7 D) Fig. 14 = Lacrymaria sp. (= Str. lepiotoides C.&M., in herb.)

The type collection (BERGGREN 39) is in fragmentary condition. Careful examination showed that the black coloured spores are coarsely warted, with a prominent plage and mucronate germ pore, 10-12 X 6.5-7.5 µ. Some cylindrical or subfusoid cheilocystidia with inflated apices were also observed (55-65 X 10 µ). These peculiarities place this agaric in the genus Lacrymaria Patouillard. Unfortunately two problems remained unresolved. The first is whether this particular New Zealand form should be regarded as an independent species. During our collecting trips in New Zealand, we collected on two occasions a species closely related to L. velutina (S. F. Gray). In both cases the fungus grew along roadsides. The second unresolved problem is whether the fungus is introduced or indigenous.

On the premise that the determination is correct, this coprophilous species must be added to the list of introduced fungi.

Tricholoma brevipes (Bulliard) (1, 16) = Lepista sp.

The spores of this collection (COLENSO b 411) are neither amyloid nor dextrinoid, hyaline, warted, and measured about 5-6.5 X 3.5-4 µ. As the fruiting bodies formed fairy rings and grew in fields around Napier we suspect this fungus was introduced into New Zealand with grass seeds.

Collybia bubalina Stevenson (29D) = Tricholoma bubalinum (Stevenson) comb. nov. (Basionym: C. bubalina Stevenson, Kew Bull. 19: 9, 1964) This species is a typical Tricholoma. The cuticle is formed by slightly gelatinised, cylindrical, repent hyphae without clamp connections. Spores are elliptical to subcylindric, hyaline, neither amyloid nor dextrinoid, smooth, 4.5-5 X 2-2.5 µ. Cystidia none.
The material (Sinclair and Haast 1860-61) is too fragmentary for a sound taxonomic study.

Tricholoma rutilans (Fries) (8,16) Fig. 24 = Gymnopilus crociphyllus (Cooke and Massee) Pegler

All characters of this collection (COLENSO b 972) correspond well with the type. It occurs both in Australia and New Zealand.

Probably introduced and synonymous with one of the cortinate species of Tricholoma.

Tricholoma ornaticeps Stevenson (29 D) Fig. 19 = Tricholomopsis ornaticeps (Stevenson) comb. nov. (Basionym: T. ornaticeps Stevenson, Kew Bull. 19: 17, 1964)

Examination of the type material (together with additional collection made in New Zealand) justify this proposed combination. Spores oval to subcylindrical, neither amyloid nor dextrinoid, hyaline, smooth, 7-8.5 X 4-4.5 µ. Cheilocystidia conspicuous, thin-walled, with yellow plasmatic pigment in KOH, clamp connections present. Pleurocystidia none.

This species grows in New Zealand on timber of exotic pines and may have been introduced into New Zealand.

Volvaria parvula Weinmann ined. ? = Pluteus aff. velutinornatus Stevenson

The observed characters of this collection (COLENSO b 58) are similar to those of the above-mentioned species.

Although no material of this distinct species was studied we consider that this agaric occurs in New Zealand and is an introduced fungus
The type of this species was originally found in Australia and is considered to be synonymous with Anthracophyllum archeri (see Pegler 1965).

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