Paraphoma aquatica Magana-Duenas, Stchigel & Cano-Lira
Authors/Creators
- 1. School of Pharmacy, Guiyang Healthcare Vocational University, Guiyang 550081, China
- 2. Guizhou Provincial Engineering Research Center of Medical Resourceful Healthcare Products, Guiyang Healthcare Vocational University, Guiyang 550081, China
- 3. Center for Yunnan Plateau Biological Resources Protection and Utilization College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China
- 4. Center of Excellence in Biotechnology Research (CEBR), King Saud University, Riyadh, Saudi Arabia
Description
Paraphoma aquatica Magaña-Dueñas, Stchigel & Cano-Lira Journal of Fungi 7 (12, no. 1102): 9 (2021)
Fig. 9
Description.
Saprobic on dead woody twigs of Castanopsis delavayi (Fagaceae). Sexual morph: Ascomata 110–130 × 120–130 μm (x ̄ = 122 × 126 μm, n = 5), solitary, scattered, erumpent to immersed, uni-loculate, globose to subglobose, black. Ostioles central. Peridium 7–12 μm wide, thin, comprising 3–4 layers of light brown to brown cells of textura prismatica. Hamathecium 1.5–2.5 μm wide, cylindrical, filiform, hyaline, septate, branched, cellular pseudoparaphyses, embedded in a gelatinous matrix. Asci 45–63 × 9–11 μm (x ̄ = 55 × 9.5 μm, n = 20), 8 - spored, bitunicate, fissitunicate, clavate, slightly broad at center, apically rounded, with short and rounded pedicel, minute ocular chamber. Ascospores 19–22 × 4–4.6 μm (x ̄ = 20.7 × 4.2 μm, n = 30), overlapping, biseriate, hyaline, narrowly fusiform, straight or slightly curved, with 3 transverse septa, enlarged at the second cell, constricted at the septa, smooth-walled, guttulate, without a mucilaginous sheath. Asexual morph: see Magaña-Dueñas et al. (2021).
Culture characteristics.
Ascospores germinated on PDA within 24 h at room temperature (25 ° C). Germ tubes produced from the basal and apical cells of ascospore. Colonies on PDA, reaching 25 mm diameter after 2 weeks at 20–25 ° C, mycelia superficial, medium density mycelia, entire margin, umbonate at center, band, rough surface, velvety, raised, grayish yellow, white mycelium attached to the central surface; reverse atrovirens.
Material examined.
China, Yunnan Province, Baoshan (25 ° 18 ' 48 " N, 99 ° 09 ' 50 " E), on dead woody twigs of Castanopsis delavayi (Fagaceae), 12 July 2020, G. C. Ren, BS 42 (HKAS 122713), living culture KUNCC 21-0523.
Known host, habitats, and distribution.
Capafonts and Castanopsis delavayi, freshwater submerged plant debris and terrestrial, China and Spain (Magaña-Dueñas et al. 2021; this study).
Notes.
Multi-loci phylogenetic analyses based on a concatenated LSU, ITS, tef 1 - α, rpb 2, and tub 2 sequence dataset show that our new collection (KUNCC 21-0523) formed a sister lineage to the ex-type strain of Paraphoma aquatica (FMR 16956) with solid support (100 % ML and 1.00 BYPP, Fig. 4). Sequence comparison for the ITS region between Paraphoma baoshanenses (KUNCC 21-0523) and P. aquatica (FMR 16956) showed a 6.17 % (30 / 486 bp) base pair difference, 0.12 % (2 / 848 bp) base pair difference for LSU region, 2.06 % (9 / 437 bp) base pair difference for the tef 1 - α region. Unfortunately, the morphology could not be compared as Paraphoma aquatica was reported in its asexual morph with no information on its sexual morph (Magaña-Dueñas et al. 2021). The species of Paraphoma were introduced from its asexual morph (Morgan-Jones and White 1983; de Gruyter et al. 2010; Quaedvlieg et al. 2013; Moslemi et al. 2016, 2018; Crous et al. 2017, 2021 a, 2021 b; Gomzhina et al. 2020; Magaña-Dueñas et al. 2021; Guarnaccia et al. 2022), while we introduced our new collection from its sexual morph. Therefore, we could not compare our new collection with other Paraphoma species. However, based on the phylogenetic distinctiveness, we introduce our collection as the first record of P. aquatica from Castanopsis delavayi (Fagaceae) in China, and our species is the first sexual morph recorded in this genus.
Notes
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Linked records
Additional details
Identifiers
Biodiversity
- Collection code
- HKAS, KUNCC
- Material sample ID
- HKAS 122713, KUNCC 21-0523
- Event date
- 2020-07-12
- Verbatim event date
- 2020-07-12
- Scientific name authorship
- Magana-Duenas, Stchigel & Cano-Lira
- Kingdom
- Fungi
- Phylum
- Ascomycota
- Order
- Pleosporales
- Family
- Phaeosphaeriaceae
- Genus
- Paraphoma
- Species
- aquatica
- Taxon rank
- species
References
- Magaña-Dueñas V, Cano-Lira JF, Stchigel AM (2021) New Dothideomycetes from freshwater habitats in Spain. Journal of Fungi (Basel, Switzerland) 7 (12): 1102. https://doi.org/10.3390/jof7121102
- Morgan-Jones G, White JF (1983) Studies in the genus Phoma. iii: Paraphoma, a new genus to accomodate Phoma radicina 1983. Mycotaxon 18: 57–65.
- de Gruyter J, Woudenberg JHC, Aveskamp MM, Verkley GJM, Groenewald JZ, Crous PW (2010) Systematic reappraisal of species in Phoma section Paraphoma, Pyrenochaeta and Pleurophoma. Mycologia 102 (5): 1066–1081. https://doi.org/10.3852/09-240
- Quaedvlieg W, Verkley GJM, Shin HD, Barreto RW, Alfenas AC, Swart WJ, Groenewald JZ, Crous PW (2013) Sizing up septoria. Studies in Mycology 75: 307–390. https://doi.org/10.3114/sim0017
- Moslemi A, Ades PK, Groom T, Crous PW, Nicolas ME, Taylor PWJ (2016) Paraphoma crown rot of pyrethrum (Tanacetum cinerariifolium). Plant Disease 100 (12): 2363–2369. https://doi.org/10.1094/PDIS-05-16-0628-RE
- Moslemi A, Ades PK, Crous PW, Groom T, Scott JB, Nicolas ME, Taylor PWJ (2018) Paraphoma chlamydocopiosa sp. nov. and Paraphoma pye sp. nov., two new species associated with leaf and crown infection of pyrethrum. Plant Pathology 67 (1): 124–135. https://doi.org/10.1111/ppa.12719
- Crous PW, Wingfield MJ, Burgess TI, Hardy GEStJ, Barber PA, Alvarado P, Barnes CW, Buchanan PK, Heykoop M, Moreno G (2017) Fungal Planet description sheets: 558–624. Persoonia 38: 240–384. https://doi.org/10.3767/003158517X698941
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- Crous PW, Hernández-Restrepo M, Schumacher RK, Cowan DA, Maggs-Kölling G, Marais E, Wingfield MJ, Yilmaz N, Adan OCG, Akulov A, Duarte E, Berraf-Tebbal A, Bulgakov TS, Carnegie AJ, de Beer ZW, Decock C, Dijksterhuis J, Duong TA, Eichmeier A, Hien LT, Houbraken JAMP, Khanh TN, Liem NV, Lombard L, Lutzoni FM, Miadlikowska JM, Nel WJ, Pascoe IG, Roets F, Roux J, Samson RA, Shen M, Spetik M, Thangavel R, Thanh HM, Thao LD, van Nieuwenhuijzen EJ, Zhang JQ, Zhang Y, Zhao LL, Groenewald JZ (2021 b) New and Interesting Fungi. 4. Fungal Systematics and Evolution 7 (1): 255–343. https://doi.org/10.3114/fuse.2021.07.13
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- Guarnaccia V, Martino I, Tabone G, Crous PW, Gullino ML (2022) Paraphoma garibaldii sp. nov. causing leaf spot disease of Campanula rapunculoides in Italy. Fungal Systematics and Evolution 9 (1): 19–26. https://doi.org/10.3114/fuse.2022.09.03