Fungalpedia – Note 1248, Halosphaeriaceae

 

Halosphaeriaceae E. Müll. & Arx

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

Index FungorumFacesoffungiMycoBank, GenBank.

Classification: MicroascalesHypocreomycetidae, SordariomycetesPezizomycotinaAscomycota, Fungi

Saprobic on algae, immersed or submersed on phanerogams, wood, bark, leaves, and other cellulosic plant remains, grains of sand, or on calcareous shell fragments, rarely parasitic or symbiotic, found in marine (oceans, mangroves and estuaries) and freshwater habitats. Sexual morph: Ascomata subglobose, cylindrical or pyriform, hyaline or dark; sometimes subiculate, rarely stromatic; superficial or immersed. Ostioles papillate to long cylindrical; ostiolar canal with periphyses or pseudoparenchyma; rarely without ostioles. Peridium soft or subcarbonaceous, composed of flattened, thick- or thin-walled cells. Centre of immature ascomata consisting of polygonal, thin-walled, pseudoparenchymatic cells, sometimes with pits, at maturation separating to form catenophyses or compressed by the asci and dissolving. Paraphyses absent. Asci fusiform, clavate or rarely subglobose, with or without apical structures, thin-walled, 1-layered, persistent or swelling and deliquescing at or before ascospore maturity. Hymenial layer at base of venter, flat or convex. Mature ascospores filling the venter of the ascoma, released singly through the ostiole or rarely within the ascus, which swells after dispersal. Ascospores overlapping 2-3 seriate, hyaline or light brown, 1- multi-celled, mostly with characteristic ornamentations, appendages or gelatinous sheaths, or both. Asexual morph: Hyphomycetous. Hyphae hyaline or brown, superficially or immersed, septate, branched. Conidiophores simple or micronematous, hyaline or mid to dark brown, paler towards the apex, unbranched, walls smooth, thin or thick-walled, terminal, integrated, monoblastic, determinate or arise as erect lateral branches from the cells of the vegetative hyphae, wide at the base, tapering only slightly above or arising singly or in groups of 2- 4 from a small stroma or flexuous, initially short and simple becoming longer and many times septate (up to 10), old conidiophore apices become displaced laterally as the conidiophore elongates and persists as short conoid denticles. Conidiogenous cells erect, some are with a distinct collarette, produce conidia terminally in a sympodial fashion or monoblastic, integrated, terminal, determinate. Conidia solitary, hyaline to bright reddish brown, holoblastic arising singly from the apices of the conidiogenous cells or develop as a small swelling at the end of the collarette, thinwalled, smooth, fusoid, (2) 7-11 septate, sigmoid with a flat detachment scar or initially oval gradually the upper half widens and becomes turbinate and finally triangular-shaped, each corner of the triangle with a long, hair-like divergent process or helicoids, semi-contorted, mostly coiled 0.75-1 times, 3-4 (5) septate, constricted at the septa; cells increase in size and pigments from base to apex: apical cell conspicuously swollen, subglobose, darker than the others, basal cell cylindrical and tapering (adapted from Maharachchikumbura et al. 2016b).

Notes – Halosphaeriaceae which was discussed by Müller & von Arx (1962) and Eriksson (1984) currently comprises 163 species in 64 genera (Pang 2002, Jones et al. 2009201520172019Maharachchikumbura et al. 2015Wijayawardene et al. 2017a2018a). The Halosphaeriaceae was validated by Kohlmeyer (1972) and assigned as a single family to Halosphaeriales (Hawksworth & Eriksson 1986). Halosphaeriaceae was previously polyphyletic and the genera Lulworthia and Lindra were referred to a new family Lulworthiaceae (Campbell et al. 2003Pang et al. 2003, Koch et al. 2007). Even though Hibbett et al. (2007) and Schoch et al. (2007) referred Halosphaeriaceae to Microascales, some other researchers included it in Halosphaeriales (Zhang et al. 2006Tang et al. 2007Jones et al. 2009). Recent studies by Jones et al. (2015) and Maharachchikumbura et al. (20152016b) established the placement of the Halosphaeriaceae as one of the families in the Microascales. Perithecial ascomata, necks (usually with periphyses), the presence of catenophyses that easily deliquesce, unitunicate, thin-walled asci that deliquesce early, with or lacking an apical ring and appendaged ascospores are the most common characters of this family (Jones 1995, Campbell et al. 2003Pang et al. 2003, Koch et al. 2007), while some genera have been introduced based on ascospore appendage morphology and ontogeny, such as Bovicornuta, Kohlmeyeriella, Ondiniella, and Marinospora (Jones et al. 1983, 1984, Jones 1995) but subsequently confirmed by molecular data. Halosphaeriaceous species are primarily marine, found on wood (especially mangrove wood) or seagrasses and are cosmopolitan in distribution (Jones 2011, Jones & Pang 2012Jones et al. 2013). Some species are found in freshwater habitats, which was belong to the genera Aniptodera, Lignincola, Luttrellia, Magnisphaera, Naïs, Natantispora, Oceanitis, Panorbis and Phaeonectriella and the majority are lignicolous (Pang & Jheng 2012, Cai et al. 2014). Around 75% of halosphaeriaceous species have been sequenced (Jones et al. 2017).

Type genus: Halosphaeria Linder.

 

References

Cai L, Hu DM, Liu F, Hyde KD, Jones EBG. 2014 – The molecular phylogeny of freshwater Sordariomycetes and Discomycetes. In: Jones EBG, Hyde KD and Pang KL (eds). Freshwater fungi and fungal-like organisms. De Gruyter, Berlin 45–69.

Campbell J, Anderson JL, Shearer CA. 2003 – Systematics of Halosarpheia based on morphological and molecular data. Mycologia 95, 530–552.

Eriksson OE. 1984 – Outline of the ascomycetes. Systema Ascomycetum 3, 1–72.

Hawksworth DL, Eriksson OE. 1986 – The names of accepted orders of ascomycetes. Systema Ascomycetum 5, 175–184.

Hibbett DS, Binder M, Bischoff JF, Blackwell M et al. 2007 – A higher-level phylogenetic classification of the Fungi. Mycological research 111, 509–547.

Jones EBG. 1995 – Ultras tructure and taxonomy of the aquatic ascomycetous order Halosphaeriales. Canadian Journal of Botany 73, 790–801.

Jones EBG. 2011 – Are there more marine fungi to be described? Botanica Marina 54, 343–354. Jones et Eaton (Ascomycotina). Botanica Marina 35, 83–91. 

Jones EBG, Pang KL. 2012 – Marine fungi and fungal-like organisms. Walter de Gruyter GmbH and Co. KG, Berlin/Boston. 

Jones EBG, Johnson RG, Moss ST. 1983 – Taxonomic studies of the Halosphaeriaceae: Corollospora Werdermann. Botanical Journal of the Linnean Society 87, 193–212. 

Jones EBG, Johnson RG, Moss ST. 1984 – Taxonomic studies of the Halosphaeriaceae: Halosphaeria Linder. Botanica Marina 27, 129–143. 

Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL. 2009 – Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Diversity 35, 1–187. 

Jones EBG, Alias SA, Pang KL. 2013 – Distribution of marine fungi and fungus-like organisms in the south china sea and their potential use in industry and pharmaceutical application. Malaysian Journal of Science (Special Issue) 119–130. 

Jones EBG, Suetrong S, Sakayaroj J, Bahkali AH et al. 2015 – Classification of marine Ascomycota, Basidiomycota, Blastocladiomycota and Chytridiomycota. Fungal Diversity 73, 1–72. 

Jones EBG, Ju WT, Lu CL, Guo SY, Pang KL. 2017 – The Halosphaeriaceae revisited. Botanica Marina 60, 453–468. 

Jones EBG, Pang KL, Abdel-Wahab MA, Scholz B et al. 2019 – An online resource for marine fungi. Fungal Diversity 96, 347–433. 

Koch J, Pang KL, Jones EBG. 2007 – Rostrupiella danica gen. et sp. nov., a lulworthia-like marine lignicolous species from Denmark and the USA. Bot Mar 50, 1–8.

Kohlmeyer J. 1972 – A revision of Halosphaeriaceae. Canadian Journal of Botany 50, 1951–1963.

Maharachchikumbura SSN, Hyde KD, Jones EBG, McKenzie EHC et al. 2015 – Towards a natural classification and backbone tree for Sordariomycetes. Fungal Diversity 72, 199–301.

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

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

Pang KL. 2002 – Systematics of the Halosphaeriales: which morphological characters are important? In: Hyde KD (eds). Fungi in marine environments. Fungal Diversity Press, Hong Kong 35–57.

Pang KL, Jheng JS. 2012 – A checklist of marine fungi of Taiwan with a description of Kitesporella keelungensis gen. etp. nov. Botanica Marina 55, 459–466.

Pang KL, Vrijmoed LLP, Kong RYC, Jones EBG. 2003 – Lignincola and Nais, polyphyletic genera of the Halosphaeriales (Ascomycota). Mycological Progress 2, 29–39.

Schoch CL, Sung GH, Volkmann-Kohlmeyer B, Kohlmeyer J, Spatafora JW. 2007 – Marine fungal lineages in the Hypocreomycetidae. Mycological Research 110, 257–263.

Tang AMC, Jeewon R, Hyde KD. 2007 – Phylogenetic utility of protein (RPB2, β-tubulin) and ribosomal (LSU, SSU) gene sequences in the systematics of Sordariomycetes (Ascomycota, Fungi). Antonie Van Leeuwenhoek 91, 327–349.

Wijayawardene NN, Hyde KD, Lumbsch HT, Liu JK et al. 2018a – Outline of Ascomycota: 2017. Fungal Diversity 88, 167–263.

Wijayawardene NN, Hyde KD, Rajeshkumar KC, Hawksworth DL et al. 2017a – Notes for genera: Ascomycota. Fungal Diversity 86, 1–594.

Zhang N, Castelbury LA, Miller AN, Huhndorf SM et al. 2006 – An overview of the systematics of the Sordariomycetes based on a four-gene phylogeny. Mycologia 98, 1076–1087.

 

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