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1

Li, Sai Nan, Fei Xu, Ming Jiang, Feng Liu, Fang Wu, Ping Zhang, Yu Guang Fan und Zuo Hong Chen. „Two new toxic yellow Inocybe species from China: morphological characteristics, phylogenetic analyses and toxin detection“. MycoKeys 81 (03.08.2021): 185–204. http://dx.doi.org/10.3897/mycokeys.81.68485.

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Some species of Inocybes. str. caused neurotoxic poisoning after consumption around the world. However, there are a large number of species in this genus that have not been studied for their toxicity or toxin content. In this study, we report two new toxic yellow Inocybes. str. species from China based on morphological characteristics, phylogenetic analyses and toxin detection. Among the two species, Inocybe squarrosolutea is reported as a newly recorded species of China. We also describe a new species, I. squarrosofulva, which is morphologically similar to I. squarrosolutea. The new species is characterized by its ochraceous squarrose pileus, distinctly annulate cortina on the stipe, nodulose basidiospores and thick-walled pleurocystidia. Muscarine in the fruitbodies was detected by UPLC–MS/MS, the content in I. squarrosolutea and I. squarrosofulva were 136.4 ± 25.4 to 1683.0 ± 313 mg/kg dry weight and 31.2 ± 5.8 to 101.8 ± 18.9 mg/kg dry weight, respectively.
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2

Redhead, S. A., Pierre Moenne-Loccoz und Patrick Reumaux. „Fungorum Rariorum Icones Coloratae, Pars XIX, Inocybes Critiquables et Critiques“. Mycologia 83, Nr. 3 (Mai 1991): 382. http://dx.doi.org/10.2307/3760001.

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3

Waterkeyn, L., A. Bienfait und T. Monniez. „Les cystides à cristaux des Inocybes (Agaricales): étude histochimique et cristallographique“. Canadian Journal of Botany 70, Nr. 5 (01.05.1992): 910–20. http://dx.doi.org/10.1139/b92-115.

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Histochemical and cristallographic studies were performed in light microscopy and scanning electron microscopy on crystal-bearing cystidia of several Inocybe spp. (Agaricales) and confirmed the excretory function of these sterile cells of the hymenium. At the apex of these bottle-like cells, the wall had an axial polysaccharidic matrix rich in carboxyl groups. It also presented an enhanced permeability and a local concentration of Ca2+. Functioning as an hydathode, the cystidium secreted, at its apex, an aqueous droplet into which twin crystals developed. In addition, crystal sand were found in the cystidium wall. These two crystalline products were calcium oxalate as confirmed with anthracene green and the Pizzolato test. A detailed crystallographic study showed that these twin crystals undoubtedly belong to the monoclinic system, i.e., the monohydrated form of the calcium oxalate or whewellite. In the case of Inocybe asterospora Quél., these grouped crystals were formed regularly by two pairs of twin crystals. The identification and localization of the Ca2+ ions have been determined with the scanning electron microscope by means of the X-emission pictures and the resulting energy dispersive X-spectrum for the latter element. Key words: Inocybe, cystidium, hydathode, calcium oxalate, whewellite.
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4

Kobayashi, Takahito, und Seishi Onishi. „Inocybe sericella, a new species of Inocybe sect. Inocybe [= Cortinatae] from Kobe, Japan“. Nova Hedwigia 90, Nr. 1 (01.02.2010): 227–32. http://dx.doi.org/10.1127/0029-5035/2010/0090-0227.

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5

Turnbull, E. „Inocybe in Peninsular Malaysia“. Edinburgh Journal of Botany 52, Nr. 3 (November 1995): 351–59. http://dx.doi.org/10.1017/s0960428600002043.

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Nine species of Inocybe (Basidiomycotina, Cortinariaceae) are described from Malaysia. Inocybe aurantiocystidiata is described as a new species and I. palaeotropica is proposed as a new name. Astrosporina aequalis is combined in Inocybe.
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6

Hobart, Carol, und Mario Tortelli. „Inocybe bresadolae“. Field Mycology 10, Nr. 1 (Januar 2009): 9–10. http://dx.doi.org/10.1016/s1468-1641(10)60489-6.

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7

Cullington, Penny, und Alan Outen. „Inocybe erinaceomorpha“. Field Mycology 10, Nr. 1 (Januar 2009): 11–14. http://dx.doi.org/10.1016/s1468-1641(10)60490-2.

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8

Bandini, Ditte, Bernd Oertel, Pierre-Arthur Moreau, Marco Thines und Sebastian Ploch. „Three new hygrophilous species of Inocybe, subgenus Inocybe“. Mycological Progress 18, Nr. 9 (September 2019): 1101–19. http://dx.doi.org/10.1007/s11557-019-01509-y.

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9

Marfi, Wa Ode Ernawati. „Keanekaragaman Fungi Ektomikoriza di Hutan Pinus merkusii Desa Matarawa Kecamatan Watopute Kabupaten Muna“. Agrikan: Jurnal Agribisnis Perikanan 11, Nr. 2 (17.11.2018): 116. http://dx.doi.org/10.29239/j.agrikan.11.2.116-123.

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Tujuan dari penelitian ini adalah untuk mengetahui nilai indeks keanekaragaman jenis-jenis fungi ektomikoriza di bawah tegakan Pinus merkusii di Desa Matarawa. Penelitian ini menggunakan metode survei yaitu secara sensus. Fungi ektomikoriza yang ditemukan di lokasi I yaitu Inocybe sp. 1, Inocybe sp. 2, Inocybe sp. 3, Inocybe sp. 4, dan Russula sp. 1. Fungi ektomikoriza yang hanya dapat ditemukan di Desa Matarawa lokasi II yaitu Inocybe sp. 5, Russula sp. 2 dan Amanita sp. 1. Fungi ektomikoriza yang hanya dapat ditemukan di Desa Matarawa lokasi III yaitu Amanita sp.2. Terdapat perbedaan nilai indeks keanekaragaman di ketiga lokasi penelitian, lokasi I yaitu 1,209, lokasi II yaitu 0,765, sedangkan nilai 0,00 berasal dari lokasi III. Nilai yang ada menunjukkan nilai yang rendah dan sangat rendah.
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10

Braaten, Christine C., P. Brandon Matheny, Debra L. Viess, Michael G. Wood, Joseph H. Williams und Neale L. Bougher. „Two new species of Inocybe from Australia and North America that include novel secotioid forms“. Botany 92, Nr. 1 (Januar 2014): 9–22. http://dx.doi.org/10.1139/cjb-2013-0195.

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The secotioid form of fruit bodies of mushroom-forming fungi may be an intermediate evolutionary modification of epigeous agaricoid or pileate–stipitate forms (i.e., with pileus, spore-bearing tissues, and stipe) and typically hypogeous, gasteroid- or truffle-forming species, in which the fruit bodies have been reduced to enclosed structures containing modified spore-producing tissues. To date, only a single secotioid species (Auritella geoaustralis Matheny & Bougher ex Matheny & Bougher) has been described in the ectomycorrhizal family Inocybaceae, a hyperdiverse clade of ca. 500–700 species with a cosmopolitan distribution. Fieldwork in Australia and western North America, however, has revealed two novel secotioid forms of Inocybe (Fr.) Fr., the first to be formally described in the genus. In this investigation, we analyze their phylogenetic relationships using molecular sequence data from multiple unlinked loci to test whether these are environmental variants of agaricoid forms or represent independent lineages. Results of phylogenetic analyses suggest these fungi have converged to the secotioid form independently. However, the California secotioid taxon (Inocybe multifolia f. cryptophylla f. nov.) is a phenotypic variant of the newly described agaricoid taxon (Inocybe multifolia sp. nov.). Similarly, the Australian secotioid form (Inocybe bicornis f. secotioides f. nov.) is nested within a clade of otherwise agaricoid forms of a second novel species (Inocybe bicornis sp. nov.) described from southwest Western Australia. Overall, four species with sequestrate forms within Inocybaceae can now be recognized, three of which are distributed in Australia and one in western North America, in the genera Auritella and Inocybe.
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11

Vauras, Jukka, und Katri Kokkonen. „Finnish records on the genus Inocybe: the new species Inocybe saliceticola“. Karstenia 48, Nr. 2 (2009): 57–67. http://dx.doi.org/10.29203/ka.2009.429.

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12

Kumar, J., und N. S. Atri. „Characterisation and identification of ectomycorrhizae formed by the species of Asproinocybe (Tricholomataceae) and Inocybe (Inocybaceae) with the roots of the tropical sal tree Shorea robusta (Dipterocarpaceae)“. Ukrainian Botanical Journal 78, Nr. 2 (30.04.2021): 112–22. http://dx.doi.org/10.15407/ukrbotj78.02.112.

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In the course of the present study, surveys on occurrence and distribution of ectomycorrhizal (EcM) fungi in tropical sal forests of foothills of the Himalayas, India, were undertaken. The species of two genera of agarics, namely Asproinocybe and Inocybe, were found organically associated with the roots of Shorea robusta (sal tree). However, prior to our study the genus Asproinocybe has not been reported from India. In this article, the morpho-anatomical details of mycorrhizal roots of Shorea robusta associated with Asproinocybe lactifera and Inocybe purpureoflavida are provided for the first time. The EcM colonized roots of the two species are distinguished by differences in the shape and colour of the roots, surface texture, size and shape of cystidia, type of mantle, as well as different chemical reactions. Asproinocybe lactifera EcM is mainly characterised by a monopodial pinnate mycorrhizal system with the dark brown to reddish brown and loose cottony surface, while in Inocybe purpureoflavida it is irregularly pinnate to coralloid, silvery grey to reddish brown, with densely woolly surface. The outer mantle layer is heterogeneous with obclavate to awl-shaped cystidia in Asproinocybe lactifera, whereas Inocybe purpureoflavida EcM have a plectenchymatous outer mantle with subcylindrical to obclavate metuloidal and non-metuloidal cystidia. The presence of lactifers in the mantle is a unique feature in Asproinocybe lactifera as compared to Inocybe purpureoflavida.
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13

DOVANA, FRANCESCO, ENRICO BIZIO, MATTEO GARBELOTTO und GIULIANO FERISIN. „Inocybe cervenianensis (Agaricales, Inocybaceae), a new species in the I. flavoalbida clade from Italy“. Phytotaxa 484, Nr. 2 (17.02.2021): 227–36. http://dx.doi.org/10.11646/phytotaxa.484.2.7.

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The authors describe the macro- and microscopic features of Inocybe cervenianensis, a new taxon belonging to the genus Inocybe sensu stricto. The description is illustrated with photographs of the basidiomes in their natural habitat and photographs of the main microscopic features. Molecular data (nrITS and RPB2) support the recognition of this new species.
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14

Patocka, Jiri, Ran Wu, Eugenie Nepovimova, Martin Valis, Wenda Wu und Kamil Kuca. „Chemistry and Toxicology of Major Bioactive Substances in Inocybe Mushrooms“. International Journal of Molecular Sciences 22, Nr. 4 (23.02.2021): 2218. http://dx.doi.org/10.3390/ijms22042218.

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Mushroom poisoning has always been a threat to human health. There are a large number of reports about ingestion of poisonous mushrooms every year around the world. It attracts the attention of researchers, especially in the aspects of toxin composition, toxic mechanism and toxin application in poisonous mushroom. Inocybe is a large genus of mushrooms and contains toxic substances including muscarine, psilocybin, psilocin, aeruginascin, lectins and baeocystin. In order to prevent and remedy mushroom poisoning, it is significant to clarify the toxic effects and mechanisms of these bioactive substances. In this review article, we summarize the chemistry, most known toxic effects and mechanisms of major toxic substances in Inocybe mushrooms, especially muscarine, psilocybin and psilocin. Their available toxicity data (different species, different administration routes) published formerly are also summarized. In addition, the treatment and medical application of these toxic substances in Inocybe mushrooms are also discussed. We hope that this review will help understanding of the chemistry and toxicology of Inocybe mushrooms as well as the potential clinical application of its bioactive substances to benefit human beings.
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15

Pošta, Ana, Ditte Bandini, Armin Mešić, Lucia Pole, Ivana Kušan, Neven Matočec, Olga Malev und Zdenko Tkalčec. „Inocybe istriaca sp. nov. from Brijuni National Park (Croatia) and Its Position within Inocybaceae Revealed by Multigene Phylogenetic Analysis“. Diversity 15, Nr. 6 (08.06.2023): 755. http://dx.doi.org/10.3390/d15060755.

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Integrative taxonomic studies of macrofungal diversity in the Brijuni National Park (Istria County, Croatia) led to the discovery of a second species of Inocybe (Agaricales, Inocybaceae) new to science. Inocybe istriaca sp. nov. is described on the basis of morphological, ecological, and multigene phylogenetic analyses, and its placement within the family Inocybaceae is discussed. The combination of most important morphological characters that distinguish I. istriaca from the other similar Inocybe species are smooth, (sub)amygdaliform, (sub)phaseoliform, or ellipsoid basidiospores (ca. 8.5–12 × 5–7 μm), large basidia (36–45 × 9–15 μm), mostly (sub)fusiform and weakly thick-walled (up to 1.5 μm) metuloid pleurocystidia, and lamellar edge and stipe apex partially covered by a dark resinous substance. The species was collected on the edge of grassland and Mediterranean evergreen holm oak (Quercus ilex) forest. In this study, a total of 14 DNA sequences from four Inocybe species were generated. Two-gene (ITS, LSU) and four-gene (ITS, LSU, rpb2, tef1) phylogenetic analyses confirmed the status of I. istriaca as an independent species.
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16

Razzaq, Annum, Arooj Naseer und Abdul Nasir Khalid. „Inocybe subhimalayanensis (Agaricales, Inocybaceae), a new smooth spored Inocybe species from Pakistan“. European Journal of Taxonomy 870 (17.05.2023): 76–86. http://dx.doi.org/10.5852/ejt.2023.870.2119.

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During mycological explorations, a new smooth spored species, Inocybe subhimalayanensis Razzaq, Naseer & Khalid sp. nov. was collected from moist temperate sub-Himalayan region, Pakistan. Phylogeny of ITS and LSU regions of nrDNA, and morphoanatomical data make it distinct from other known species of the genus. The taxon is characterized by: a yellowish orange to brown pileus with prominent fibrillose, prominent umbo; ellipsoid to amygdaliform smooth larger basidiospores (8.4‒)8.6‒12.2(‒12.6) × (4.9‒)5.1‒7.1(‒7.3) µm; and lack of velipellis. Molecular phylogenetic analyses further support the recognition of the new species.
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17

DOVANA, FRANCESCO, GIULIANO FERISIN, ENRICO BIZIO, DITTE BANDINI, IBAI OLARIAGA und FERNANDO ESTEVE-RAVENTÓS. „A morphological and phylogenetic characterisation of Inocybe similis (Agaricales, Inocybaceae), a rare species described by Bresadola in 1905“. Phytotaxa 474, Nr. 1 (27.11.2020): 71–80. http://dx.doi.org/10.11646/phytotaxa.474.1.7.

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Inocybe similis, a very rare smooth-spored species originally described from Italy by Bresadola, is illustrated. Based on sequence generated from the type specimen, freshly collected specimens from five sites, Grado in north-east Italy, Tolmin in Slovenia, Forchach and Rieden in Austria and Füssen in Gemany could be asigned to I. similis and a more detailed description is provided here. The macro- and micromorphological features of I. similis suggest this species should be placed in Inocybe sect. Splendentes according to Singer´s classification. In contrast, our phylogenetic analyses support instead that I. similis belongs to Inocybe sect. Marginatae. From a morphological point of view, I. similis is close to I. vulpinella, but it is phylogenetically close to I. flavobrunnescens in sect. Marginatae.
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Raghoonundon, Bhavesh, Santhiti Vadthanarat, Yuwei Hu und Olivier Raspé. „Inocybe hopeae sp. nov. and first record of Pseudosperma keralense (Inocybaceae) from Thailand“. European Journal of Taxonomy 870 (09.05.2023): 30–45. http://dx.doi.org/10.5852/ejt.2023.870.2115.

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Based on genetic studies, supported further by morphological and ecological differences, we present a taxonomic novelty (Inocybe hopeae Raghoonundon & Raspé sp. nov.) and a new geographical record (Pseudosperma keralense) from forests of Northern Thailand. Inocybe hopeae is characterized by medium-sized basidiomes, brownish orange to brown pileus that is darker towards the margin, off-white to pale brown context, light brown to dark brown stipe with off-white basal mycelium and pale brown to grayish brown lamellae. A three-gene phylogeny (LSU, tef1, rpb2) coupled with macroscopic / microscopic descriptions and illustrations are provided confirming the species’ positions in their respective generic clades. Inocybe hopeae was sister to I. thailandica with strong support (BS = 100%, PP = 1.0). Our Thai collections of OR1629 had similar morphological characters and 100% identical sequences with the holotype of Pseudosperma keralense from India.
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19

KAYGUSUZ, OĞUZHAN, DITTE BANDINI und ALİ ÇELİK. „Inocybe kusadasiensis (Inocybaceae: Agaricomycetes), a new species from Turkey“. Phytotaxa 570, Nr. 1 (25.10.2022): 1–15. http://dx.doi.org/10.11646/phytotaxa.570.1.1.

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Inocybe kusadasiensis sp. nov., a novel species which was collected from Pinus brutia forest near Kuşadası (Turkey), in the coastal area of Aegean Sea, is introduced with full descriptions of macro and microscopic features, field photograph and line-drawings. A phylogenetic analysis of sequence data for the nuc rDNA internal transcribed spacer region ITS1-5.8S-ITS2 (ITS) indicated and supported the taxonomic uniqueness of the present new species which belongs to the genus Inocybe.
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20

Obase, Keisuke, Toshizumi Miyamoto, Yutaka Tamai, Takashi Yajima und Takahito Kobayashi. „Inocybe nitidiuscula, new to Japan“. Mycoscience 47, Nr. 5 (Oktober 2006): 293–97. http://dx.doi.org/10.1007/s10267-006-0304-x.

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21

Hobart, Caroline, und Alick Henrici. „Inocybe Mytiliodora New to Britain“. Field Mycology 12, Nr. 3 (Juli 2011): 77–80. http://dx.doi.org/10.1016/j.fldmyc.2011.06.003.

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22

Cullington, Penny. „Some new British Inocybe species“. Field Mycology 14, Nr. 1 (Januar 2013): 17–20. http://dx.doi.org/10.1016/j.fldmyc.2012.12.006.

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23

LATHA, K. P. DEEPNA, und PATINJAREVEETTIL MANIMOHAN. „Inocybe gregaria, a new species of the Inosperma clade from tropical India“. Phytotaxa 286, Nr. 2 (29.11.2016): 107. http://dx.doi.org/10.11646/phytotaxa.286.2.5.

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Inocybe gregaria sp. nov. is described from Kerala State, India, based on morphological and molecular data. A comprehensive description, photographs, and comparisons with phenetically similar and phylogenetically related species are provided. The nuclear ribosomal internal transcribed spacer region (nrITS), a portion of the nuclear ribosomal large subunit (nrLSU) and a portion of the nuclear second-largest subunit of RNA polymerase II (rpb2) gene of this species were sequenced and analyzed. BLASTn searches using LSU and rpb2 sequences and subsequent ML phylogram of combined LSU and rpb2 sequences revealed that I. gregaria is conspecific with Inocybe sp. ZT8944, a collection assigned to the Inosperma clade that remains undescribed.
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24

Vauras, Jukka. „Inocybe sectio Calosporae in NW Europe“. Karstenia 28, Nr. 2 (1988): 79–86. http://dx.doi.org/10.29203/ka.1988.267.

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25

Seok, Soon-Ja, Yang-Sup Kim, So-Hyun Park, Kyong-Hee Min und Kwan-Hee Yoo. „Taxonomic Study on Inocybe in Korea“. Mycobiology 28, Nr. 3 (September 2000): 149–52. http://dx.doi.org/10.1080/12298093.2000.12015741.

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26

Gartz, Jochen. „Psilocybin in Mycelkulturen von Inocybe aeruginascens“. Biochemie und Physiologie der Pflanzen 181, Nr. 7 (Januar 1986): 511–17. http://dx.doi.org/10.1016/s0015-3796(86)80042-7.

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27

RODRÍGUEZ-CAMPO, FRANCISCO J., DITTE BANDINI und IBAI OLARIAGA. „Inocybe hamadryadis (Inocybaceae, Agaricales), a new smooth-spored species from Europe and West Asia“. Phytotaxa 594, Nr. 3 (28.04.2023): 191–203. http://dx.doi.org/10.11646/phytotaxa.594.3.3.

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Inocybe hamadryadis sp. nov. is described and a detailed description, colour photographs, microdrawings and photographs of the microscopic features are provided. The type was found under Quercus ilex and Cistus ladanifer in Mediterranean habitat in Spain, but its distribution is throughout Europe and the West Asia. Inocybe hamadryadis is characterized by a finely textured, pale to dark brown or chestnut brown pileus with a faintly greyish velipellis, smooth basidiospores, hymenial cystidia with sinuous walls and caulocystidia only near the extreme apex of the stipe. Our analyses of the ITS and LSU regions, including coded indel information, indicate that I. hamadryadis is closely related to I. tenuicystidiata, from which it differs in several morphological features, such as the smaller basidiospores on average and the shorter caulocystidia.
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Bandini, Ditte, Jukka Vauras, Øyvind Weholt, Bernd Oertel und Ursula Eberhardt. „Inocybe woglindeana, a new species of the genus Inocybe, thriving in exposed habitats with calcareous sandy soil“. Karstenia 58, Nr. 1 (2020): 41–59. http://dx.doi.org/10.29203/ka.2020.488.

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29

Kiyashko, A. A. „Three new for Russia species of dark-spored agarics (Agaricales, Basidiomycota) from Western Caucasus“. Novosti sistematiki nizshikh rastenii 45 (2011): 101–9. http://dx.doi.org/10.31111/nsnr/2011.45.101.

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Three new for Russia agaric species were found in Western Caucasus: Galerina pruinatipes, Inocybe dunensis and Cortinarius melanotus. The data on their localities as well as specimens descriptions and drawings of microfeatures are given.
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30

Cripps, Cathy L. „The Genus Inocybe in Montana Aspen Stands“. Mycologia 89, Nr. 4 (Juli 1997): 670. http://dx.doi.org/10.2307/3761005.

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31

Naseer, A., S. Ghani, A. R. Niazi und A. N. Khalid. „Inocybe caroticolor from oak forests of Pakistan“. Mycotaxon 134, Nr. 2 (01.06.2019): 241–51. http://dx.doi.org/10.5248/134.241.

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32

Watling, Roy. „An unusual Inocybe sp. from West Africa.“ Czech Mycology 52, Nr. 4 (05.03.2001): 329–34. http://dx.doi.org/10.33585/cmy.52413.

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33

Cullington, Penny. „Coming soon! Changes affecting the genus Inocybe“. Field Mycology 21, Nr. 3 (Juli 2020): 102–7. http://dx.doi.org/10.1016/j.fldmyc.2020.07.007.

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34

LATHA, K. P. DEEPNA, PATINJAREVEETTIL MANIMOHAN und P. BRANDON MATHENY. „A new species of Inocybe representing the Nothocybe lineage“. Phytotaxa 267, Nr. 1 (30.06.2016): 40. http://dx.doi.org/10.11646/phytotaxa.267.1.4.

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Inocybe distincta sp. nov. is described from Kerala State, India. A comprehensive description, photographs, line drawings and comments are provided. The nuclear ribosomal internal transcribed spacer region (ITS), a portion of the nuclear ribosomal large subunit (nrLSU) and a portion of the nuclear second-largest subunit of RNA polymerase II (RPB2) gene of this species were sequenced and analyzed. BLASTn searches using nrLSU and RPB2 sequences and subsequent ML phylogenetic analysis of combined nrLSU and RPB2 sequences confirmed that Inocybe distincta is a representative of the Nothocybe lineage. As the Nothocybe lineage is assumed to have affinities to I. cutifracta, and as there are different interpretations of that species, we examined the holotype of I. cutifracta collected by T. Petch and another collection from Sri Lanka identified as I. cutifracta by D. N. Pegler, and we present here our observations on these collections.
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35

Halling, Roy E., und Thomas W. Kuyper. „A Revision of the Genus Inocybe in Europe. I. Subgenus Inosperma and the Smooth-Spored Species of Subgenus Inocybe.“ Brittonia 39, Nr. 3 (Juli 1987): 406. http://dx.doi.org/10.2307/2807145.

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36

Esteve-Raventós, Fernando, Gabriel Moreno, Pablo Alvarado und Ibai Olariaga. „Unraveling the Inocybe praetervisa group through type studies and ITS data: Inocybe praetervisoides sp. nov. from the Mediterranean region“. Mycologia 108, Nr. 1 (Januar 2016): 123–34. http://dx.doi.org/10.3852/15-053.

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37

Liu, Dong-Ze, Qi Liu, Ping Yang und Wen-Xia Jiang. „A New Ergostane Triterpenoid from a Solid Culture of the Basidiomycete Inocybe lilacina“. Zeitschrift für Naturforschung C 69, Nr. 3-4 (01.04.2014): 89–91. http://dx.doi.org/10.5560/znc.2013-0127.

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1 A new and rare ergostane triterpenoid, 4α-methyl-3α,4β-dihydroxy-ergost-8,24(28)-dien-7,11- dion-25-al (), was isolated from cultures of the basidiomycete Inocybe lilacina, and its structure established on the basis of spectral methods (MS, IR, 1D and 2D NMR).
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38

JABEEN, Sana, Ishtlaq AHMAD, Abdur RASHID und Abdul Nasir KHALID. „Inocybe kohistanensis, a new species from Swat, Pakistan“. TURKISH JOURNAL OF BOTANY 40 (2016): 312–18. http://dx.doi.org/10.3906/bot-1501-17.

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39

Matheny, P. Brandon, und Neale L. Bougher. „Replacement names for two Australian species of Inocybe“. Mycotaxon 133, Nr. 1 (24.04.2018): 173–74. http://dx.doi.org/10.5248/133.173.

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40

Fan, Yu-Guang, und Tolgor Bau. „Two striking Inocybe species from Yunnan Province, China“. Mycotaxon 123, Nr. 1 (01.08.2013): 169–81. http://dx.doi.org/10.5248/123.169.

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41

Khan, Muhammad, Arooj Naseer, Fauzia Aqdus, Muhammad Ishaq, Muhammad Fiaz und Abdul Nasir Khalid. „Inocybe quercicola sp. nov. (Agaricales, Inocybaceae), from Pakistan“. Microbial Biosystems 6, Nr. 2 (18.02.2022): 22–29. http://dx.doi.org/10.21608/mb.2022.109930.1047.

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42

Cullington, Penny. „Inocybe lindrothii – new to the UK in 2020“. Field Mycology 22, Nr. 3 (Juli 2021): 98–100. http://dx.doi.org/10.1016/j.fldmyc.2021.07.009.

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43

Wartchow, F. „Inocybe cavalcantiae, a new species from northern Brazil“. Studies in Fungi 5, Nr. 1 (2020): 1–5. http://dx.doi.org/10.5943/sif/5/1/1.

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44

Shannon, Gerald. „A key to the genus Inocybe — Software review“. Mycologist 10, Nr. 1 (Februar 1996): 41–42. http://dx.doi.org/10.1016/s0269-915x(96)80055-3.

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45

Kobayashi, Takahito. „Notes on the genus Inocybe of Japan: II“. Mycoscience 44, Nr. 5 (Oktober 2003): 383–88. http://dx.doi.org/10.1007/s10267-003-0123-2.

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46

Kobayashi, Takahito. „Notes on the genus Inocybe of Japan: III“. Mycoscience 46, Nr. 3 (Juni 2005): 184–91. http://dx.doi.org/10.1007/s10267-005-0232-1.

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47

Kobayashi, Takahito. „Notes on the genus Inocybe of Japan: I“. Mycoscience 43, Nr. 3 (Juni 2002): 207–11. http://dx.doi.org/10.1007/s102670200030.

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48

Bandini, Ditte, Bernd Oertel, Sebastian Ploch, Tahir Ali, Jukka Vauras, Anja Schneider, Markus Scholler, Ursula Eberhardt und Marco Thines. „Revision of some central European species of Inocybe (Fr.: Fr.) Fr. subgenus Inocybe, with the description of five new species“. Mycological Progress 18, Nr. 1-2 (24.10.2018): 247–94. http://dx.doi.org/10.1007/s11557-018-1439-9.

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49

Liu, Dong-Ze, Qi Liu, Ping Yang und Wen-Xia Jiang. „A New Ergostane Triterpenoid from Cultures of the Basidiomycete Inocybe lilacina“. Natural Product Communications 9, Nr. 3 (März 2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900322.

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A new ergostane triterpenoid (4α-methylergost-8,24(28)-dien-3,7,11-trione, 1) together with four known compounds (2–5) were isolated from cultures of the basidiomycete Inocybe lilacina. The structure of the new compound was established on the basis of IR, 1D and 2D NMR spectroscopic and MS experiments.
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50

Cripps, Cathy, und O. K. Miller Jr. „Ectomycorrhizal fungi associated with aspen on three sites in the north-central Rocky Mountains“. Canadian Journal of Botany 71, Nr. 11 (01.11.1993): 1414–20. http://dx.doi.org/10.1139/b93-170.

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Sporocarps of ectomycorrhizal fungi were collected over three field seasons in aspen (Populus tremuloides) stands in the Rocky Mountains, 1800–2000 m above sea level. The two sites in southwestern Montana and one site in southeastern Idaho vary in size, age of trees, type of soil, drainage patterns, and to a certain extent, climatic conditions. In all, 43 species of ectomycorrhizal fungi were found associated with aspen. The Cortinariaceae were a dominant component of the mycoflora, including at least seven species of Inocybe. Fourteen species of ectomycorrhizal fungi, including Leccinum aurantiacum, occurred on all three sites in association with aspen, and the dominant or characteristic mycorrhizal species varied among sites. The early colonizers Inocybe lacera and Laccaria laccata, which were previously reported on acidic soil, were characteristic of the smelter-acidified, nutrient-poor soil of the site near Butte, Montana. Late stage fungi such as Amanita muscaria and Lactarius controversus were more prevalent in the older, undisturbed aspen stands. Key words: aspen, ectomycorrhizal fungi, mycorrhizal fungi, Populus tremuloides.
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