Ophiodeira Kohlm. & Volkm. - Kohlm.
- Dayarathne, Monika C.1
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Jones, E. B. Gareth2
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Bahkali, Ali H.2
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Devadatha, Bandarupalli3
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Hyde, Kevin D.4
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Abdel-Wahab, Mohamed A.5
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Calabon, Mark S.6
- Correia, Pedro7
- Abdel-Aziz, Faten A.5
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Bakhit, Mahmoud S.5
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Sakayaroj, Jariya8
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Prematunga, Chasika4
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Caeiro, Maria F.7
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Azevedo, Egídia7
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Asghari, Raheleh4
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Apurillo, Carlo Chris S.4
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Bhagya, Amuhenage Tharindu4
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Aumentado, Herbert Dustin4
- Mukhopadhyay, Samhita4
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Phukhamsakda, Chayanard4
- Chen, Yanpeng9
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Maharachchikumbura, Sajeewa S.10
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Guo, Sheng-Yu11
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Pang, Ka-Lai11
- 1. Department of Plant Science, Agriculture Building, University of Manitoba, Winnipeg, Manitoba R 3 T 2 N 2, Canada & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand
- 2. Department of Botany and Microbiology, King Saudi University, Riyadh, Saudi Arabia
- 3. Microbial Type Culture Collection and Gene Bank (MTCC), CSIR-Institute of Microbial Technology, Chandigarh, 160036, India & Fungal Biotechnology Lab, Department of Biotechnology, School of Life Sciences, Pondicherry University, Kalapet, Pondicherry- 605014, India
- 4. Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand
- 5. Department of Botany and Microbiology, Faculty of Science, Sohag University, Sohag 82524, Egypt
- 6. Division of Biological Sciences, College of Arts and Sciences, University of the Philippines Visayas, Miagao, Iloilo, 5023 Philippines
- 7. CE 3 C – Centre for Ecology, Evolution and Environmental Changes, Departamento de Biologia (DBio), Faculdade de Ciências da Universidade de Lisboa (FCUL), Campo Grande 1749 - 016, Lisbon, Portugal & CHANGE – Global Change and Sustainability Institute, Departamento de Biologia (DBio), Faculdade de Ciências da Universidade de Lisboa (FCUL), Campo Grande 1749 - 016, Lisbon, Portugal
- 8. Department of Biology School of Science, Walailak University, 222 Thaiburi, Thasala district, Nakhon Si Thammarat 80161, Thailand
- 9. Archaeal Biology Center, Institute for Advanced Study, Shenzhen University, Shenzhen, China & College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China
- 10. School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China
- 11. Institute of Marine Biology and Center of Excellence for the Oceans, National Taiwan Ocean University, 2 Pei-Ning Road, Keelung 202301, Taiwan
Description
Ophiodeira Kohlm. & Volkm. - Kohlm., Canad. J. Bot. 66 (10): 2062 (1988)
Description.
Saprobic on submerged woody substrates in marine habitats. Sexual morph. Ascomata ellipsoidal, immersed under a thin black stroma, ostiolate, light brown, solitary or gregarious, neck elongated, periphysate. Peridium thin, forming textura angularis. Catenophyses absent. Asci 8 - spored, clavate, pedunculate, thin-walled, unitunicate, deliquescing early, lacking an apical apparatus. Ascospores hyaline, 1 - septate, ellipsoidal, not constricted at the septum, with a single polar appendage, initially hamate, separating from the spore wall and eventually uncoiling to form long, sticky filaments. Asexual morph. Undetermined.
Type species.
Ophiodeira monosemeia Kohlm. & Volkm. - Kohlm., Canad. J. Bot. 66 (10): 2062 (1988).
Notes.
The monotypic genus, Ophiodeira is characterized by ascospores with a single polar appendage uncoiling to form sticky filaments, as found in the genera: Halosarpheia, Ascosacculus and Magnisphaera. Ophiodeira differs from the three previous genera by having ascomata that are immersed under a thin black stroma, deliquescing asci, absence of catenophyses and a single ascospore appendage that is cap-like, attached to the apex and side of the ascospore, at first stiff and homogenous, in water becoming soft and banner-like, eventually transforming into a coil of delicate fibers that uncoil and form long, sticky filaments (Kohlmeyer and Volkmann-Kohlmeyer 1988; Jones et al. 2009).
Ophiodeira closely resembles Tirispora in that both genera have a single polar appendage that unfurls in water. However, both genera differ in that Ophiodeira has ascomata produced under a thin, black stroma, lacks catenophyses, asci deliquesce at maturity and lacks an apical pore in the ascus (Jones et al. 1994).
Molecular evaluation.
Ophiodeira formed a highly supported monophyletic clade sister to Oceanitis species (Campbell et al. 2003; Pang et al. 2003 b; Sakayaroj et al. 2011), and this is confirmed in the present study (Fig. 4). Further collections and sequences are required as only one strain (JK 5164 A) from the type material, has been sequenced. Divergence-time analysis places the split between Ophiodeira and Oceanitis near the mid-Cretaceous (~ 105 MYA, 95 % CI: 26.6–414 MYA), underscoring their independent generic status (Fig. 5).
Notes
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Linked records
Additional details
Identifiers
Biodiversity
- Scientific name authorship
- Kohlm. & Volkm. - Kohlm.
- Kingdom
- Fungi
- Phylum
- Ascomycota
- Order
- Microascales
- Family
- Halosphaeriaceae
- Genus
- Ophiodeira
- Taxon rank
- genus
References
- Kohlmeyer J, Volkmann-Kohlmeyer B (1988) Ophiodeira gen. nov. (Halosphaeriales) and a survey of higher marine fungi from Saint Croix (Virgin Islands). Canadian Journal of Botany 66: 2062–2067. https://doi.org/10.1139/b88-282
- Jones EBG, Sakayaroj J, Suetrong S, Somrithipol A, Pang KL (2009) Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Diversity 35: 1–187.
- Jones EBG, Vrijmoed LLP, Read SJ, Moss ST (1994) Tirispora, a new genus in the Halosphaeriales. Canadian Journal of Botany 72: 1373–1378. https://doi.org/10.1139/b94-168
- Campbell J, Anderson JL, Shearer CA (2003) Systematics of Halosarpheia based on morphological and molecular data. Mycologia 95: 530–552. https://doi.org/10.1080/15572536.2004.11833100
- Pang KL, Vrijmoed LLP, Kong RYC, Jones EBG (2003 b) Polyphyly of Halosarpheia (Halosphaeriales, Ascomycota): implications on the use of unfurling ascospore appendage as a systematic character. Nova Hedwigia 77: 1–18. https://doi.org/10.1127/0029-5035/2003/0077-0001
- Sakayaroj J, Pang KL, Jones EBG (2011) Multi-gene phylogeny of the Halosphaeriaceae: its ordinal status, relationships between genera and morphological character evolution. Fungal Diversity 46: 87–109. https://doi.org/10.1007/s13225-010-0072-y