Fungalpedia – Note 1925, Phyllachoraceae

 

Phyllachoraceae. Theiss. & P. Syd.

Citation when using this data: Hyde KD et al. 2020 (in prep.) – Fungalpedia, Ascomycota.

Index FungorumFacesoffungiMycoBankGenBank

Classification: PhyllachoraceaePhyllachoralesSordariomycetidaeSordariomycetesPezizomycotinaAscomycota, Fungi

 

Parasitic on living leaves or saprobic on dead wood submerged in water. Sexual morph: Leaf spots on host black, abundant, scattered, raised, mostly rounded to oblong or elongated, sometimes parallel with leaf venation, surrounded by light brown necrotic region. Ascomata flattened, globose to subglobose, with thin walls, lying in leaf tissues or in a pseudostroma or stroma and maturing in living leaves, ostiolate. Ostiolar canal conical, wide, lacking periphyses. Peridium clypeate, thickest adjacent to ostiolar canal, composed of a deeply melanized, brown-black, amorphous layer of host cuticle and epidermal cells, often merging with a lighter pigmented region of brownish, distorted parenchyma cells infiltrated with fungal hyphae, beneath the clypeus. Lower and lateral peridium composed of two layers; an outer region comprising several layers of dark brown, flattened, thin-walled fungal cells, which internally fuse with several layers of hyaline, flattened, thin-walled fungal cells. Lateral peridium fuses outwardly with an irregular, narrow region of distorted host parenchyma infiltrated by fungal cells. The basal peridium merges outwardly with either a narrow zone of infiltrated and distorted host parenchyma and occasionally lower epidermal cells, or integrates directly with a lower clypeus, similar in construction to that basal peridium. Paraphyses numerous, persistent, filiform, branched or unbranched, septate, slightly longer than asci. Asci 8-spored, persistent, cylindrical to fusiform, short pedicellate, with walls uniform in thickness, not especially thickened at apex, apical ring often present, rarely absent, J-, or J+.

Ascospores multi-seriate, fusiform to narrowly oval, usually hyaline, aseptate or rarely septate, often with a mucilaginous sheath, with or without an attenuated base, sometimes with pad like appendages. Asexual morph: Coelomycetous, with conidia in locules in a stroma, spermatial or disseminative. Conidiomata similar to ascomata, immersed, subcuticular, strongly raising the host surface, occasionally pycnidial, occupying the region between the cuticle and epidermis, ostiolate. Conidiogenous cells arising from the basal and lateral walls, cylindrical, phialidic, aseptate, hyaline, forming conidia singly at the apex. Conidia hyaline, filiform, aseptate (adapted from Maharachchikumbura et al. 2016b). 

Notes – Theissen & Sydow (1915) introduced Phyllachoraceae, previously placed in several orders, including Dothideales (Horst 1990), Sphaeriales (Nannfeldt 1932Miller 19511954Muller & von Arx 1962Wehmeyer 1975), Xylariales (Luttrell 1951, Barr 1990a), Glomerellales (Chadefaud 1960, Locquin 1984), Phyllachorales (Barr 1976ab1983), Polystigmatales (Eriksson 1982b, Hawksworth et al. 1983), and Diaporthales (Cannon 1988). Currently, it is placed in order Phyllachorales (Maharachchikumbura et al. 2015b, 2016bSantos et al. 2016Dayarathne et al. 2017). Phyllachoraceae is characterised by ascohymenial development with paraphyses, thin-walled asci, which may have an apical ring, that does not stain blue in iodine (J-) and ascospores that are often hyaline and 1-celled (Cannon 1991). Asexual morphs are coelomycetes, spermatial or disseminative (Hawksworth et al. 1995). Munk (1957) and Barr (1990a) had a different concept of the family, including genera with J+, apical rings, in the ascus. However, in a study based on available molecular data and literature Maharachchikumbura et al. (2015, 2016b) listed 58 genera in Phyllachoraceae. Mardones et al. (2017) proposed a new family Telimenaceae with Telimena as the type genus, resulting in three families in Phyllachorales and removal of Telimena from Phyllachoraceae. Dayarathne et al. (2017) excluded Polystigma from the Phyllachorales based on analysis of combined LSU, SSU and ITS sequence data. Hence, at present family Phyllachoraceae comprises 54 genera. However, sequence data are available only for a few members of the genera Ascovaginospora, Coccodiella and Phyllachora because of the difficulties in obtaining cultures. 

The family contains a large number of species which are probably host-specific. Most genera are monotypic and the majority lack sequence data. The family therefore needs recollecting with sequence data. Many genera are poorly known and therefore the notes below are brief.

 

Type genus: Phyllachora Nitschke ex Fuckel, Jb. nassau. Ver. Naturk. 23-24: 216 (1870) [1869-70].

Other accepted species: Species Fungorum – search Phyllachoraceae.

 

References

 

Barr ME. 1976a – Buergenerula and the Physosporellaceae. Mycologia 68, 611–621.

Barr ME. 1976b – Perspectives in the Ascomycotina. Mem N Y Bot Gard 28, 1–8.

Barr ME. 1983 – The ascomycete connection. Mycologia 75, 1–13.

Barr ME. 1990a – Melanommatales (Loculoascomycetes). North American Flora, Series 2, part 13. New York Botanical Garden, New York.

Cannon PF. 1991 – A revision of Phyllachora and some similar genera on the host family Leguminosae. Mycological Papers 163, 1–302.

Chadefaud M. 1960 – Les V eg etaux non Vasculaires (Cryptogamie). In: Chadefaud M, Emberger L (eds). Trait e de Botanique Syst ematique. Masson, Paris 1–1018.

Dayarathne MC, Maharachchikumbura SSN, Jones EBG, Goonasekara ID et al. 2017 – Neophyllachora gen nov. (Phyllachorales), three new species of Phyllachora from Poaceae and resurrection of Polystigmataceae (Xylariales). Mycosphere 8, 1598–1625.

Dayarathne MC, Maharachchikumbura SSN, Jones EBG, Goonasekara ID et al. 2017 – Neophyllachora gen nov. (Phyllachorales), three new species of Phyllachora from Poaceae and resurrection of Polystigmataceae (Xylariales). Mycosphere 8, 1598–1625.

Hawksworth DL, Kirk PM, Sutton BC, Pegler DN. 1995 – Ainsworth & Bisby’s Dictionary of the fungi, 8th ed. CAB International, Wallingford, U.K.

Hawksworth DL, Lodha BC. 1983 – Helicogermslita, a new stromatic xylariaceous genus with a spiral germ slit from India. Transactions of the British Mycological Society 81, 91–96.

Horst RK. 1990 – Westcott’s plant disease handbook, 5th ed. AVI Book, USA.

Locquin M. 1984 – Mycologie générale et structurale 1–551.

Luttrell ES. 1951 – Taxonomy of the Pyrenomycetes. University of Missouri Studies 24, 1–120.

Maharachchikumbura SSN, Hyde KD, Jones EBG, McKenzie EHC et al. 2016b – Families of Sordariomycetes. Fungal Diversity 79, 1–317.

Mardones M, Trampe-Jaschik T, Oster S, Elliott M et al. 2017 – Phylogeny of the order Phyllachorales (Ascomycota, Sordariomycetes): among and within order relationships based on five molecular loci. Persoonia 39, 74–90.

Miller JH. 1951 – Studies in the Phyllachoraceae I. Phyllachora ambrosiae (Berk. and Curt.) Sacc. American Journal of Botany 38, 830–834.

Miller JH. 1954 – Studies in the Phyllachoraceae II. Phyllachora lespedezae. American Journal of Botany 41, 825–828.

Müller E, von Arx JA. 1962 – Die Gattungen der didymosporen Pyrenomyceten. Beitrage zur Kryptogamenflora der Schweiz 11, 1–922.

Munk A. 1957 – Danish Pyrenomycetes, A preliminary flora. Dansk Botanisk Arkiv 17, 1–491

Nannfeldt JA. 1932 – Studien über die Morphologie und Systematik der nichtlichenisierten inoperculaten Discomyceten. Nova Acta Regiae Societatis Scientiarum Upsaliensis 8, 1–368.

Santos MD, Fonseca-Boiteux ME, Boiteux LS, Câmara PE et al. 2016 – ITS-phylogeny and taxonomy of Phyllachora species on native Myrtacae from the Brazilian Cerrado. Mycologia 108, 1141–1164.

Theissen F, Sydow H. 1915 – Die Dothideales. Kritisch-systematische Original untersuchungen. Annales Mycologici 13, 147–746.

Wehmeyer LE. 1975 – The Pyrenomycetous Fungi. Mycologia Memoirs 6, 1–250.

 

Entry by

Kevin David Hyde, Institute of Plant Health, Zhongkai University of Agriculture and Engineering, Haizhu District, Guangzhou 510225, P.R. China, Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand, Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai 50150, Thailand, Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand, Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P.R. China, School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand, World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, P.R. China

 

Published online 28 February 2020