Camillea malaysianensis sp. nov. and the Distribution of Camillea in Southeast Asia

Whalley, M. A.; Whalley, A.J.S.; Thienhirun, Surang; Sihanonth, Prakitsin

doi:10.2307/4110867

Cited by 9 publications

(6 citation statements)

References 5 publications

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“…Ju from Costa Rica with what seems to be a germ slit and also with almost smooth spores. The genus currently comprises 33 species (35 taxa) Rogers et al 1991Rogers et al , 2002San Martín González and Rogers 1993;Whalley et al 1996Whalley et al , 1999. Most Camillea species have been found in the Neotropics and by far the largest concentration of species occurs in the Amazon region.…”

Section: Introductionmentioning

confidence: 99%

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Camillea (Xylariaceae, Ascomycota), including two new species, along a trans-Andean altitude gradient in Ecuador

Hastrup

Læssøe

2009

Mycol Progress

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Section: Introductionmentioning

confidence: 99%

“…Camillea malaysiensis M.A. Whalley (Whalley et al 1999), C. selangorensis M.A. Whalley, Whalley & E.B.G.…”

Section: Introductionmentioning

confidence: 99%

Camillea (Xylariaceae, Ascomycota), including two new species, along a trans-Andean altitude gradient in Ecuador

Hastrup

Læssøe

2009

Mycol Progress

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“…The records are from 1896 (on elm bark), 1915 (on dead Crataegus bark) and 1962 (on wind‐thrown hardwood tree) (MyCoPortal, 2024 ) Pest status in the EU Camillea tinctor is absent from the EU (Farr & Rossman, 2024 ; GBIF, 2024 ; MyCoPortal, 2024 ) Host status on Acer Camillea tinctor (as Hypoxylon tinctor ) was recorded on Acer spp. (O'Neal, 1914 ; Simmons, 1946 ), Acer floridanum , A. leucoderme , A. negundo and A. rubrum in the USA (Hanlin, 1963 ; Farr & Rossman, 2024 ) Asymptomatic plants No specific information on the presence of asymptomatic plants was found Association with wood Camillea tinctor is recorded from Africa (Congo‐Kinshasa, Ghana, Sierra Leone, Uganda), tropical America (Brazil, Cuba, French Guiana, Mexico, Nicaragua, Peru, Puerto Rico, St Croix), Australasia (Papua New Guinea), Asia (Malaysia, Singapore, Thailand) (Whalley et al., 1999 ) and North America (Calkins, 1886 ; Ellis & Everhart, 1888 ; Farr & Rossman, 2024 ; GBIF, 2024 ; MyCoPortal, 2024 ; O'Neal, 1914 ; Vasilyeva, Stephenson, & Miller, 2007 ). According to Vasilyeva et al.…”

Section: Canker Fungi and Other Fungi Associated With Sapwood ( ...mentioning

confidence: 99%

“…Stroma stain the wood with orange (Calkins, 1886 ; Miller, 1945 ; Sangvichien et al., 2013 ) to reddish‐orange colour (O'Neal, 1914 ) Temperature survival and humidity There is no information regarding lethal temperatures and humidity for this fungus Ability to produce resting propagules/chlamydospores There is no indication that C. tinctor can produce resting propagules or chlamydospores. Camillea tinctor produces stromata, asci, ascospores and perithecia (Ellis & Everhart, 1888 ; Whalley et al., 1999 ; Vasilyeva, Stephenson, & Miller, 2007 ) …”

Section: Canker Fungi and Other Fungi Associated With Sapwood ( ...mentioning

confidence: 99%

“…Camillea tinctor is recorded from Africa (Congo‐Kinshasa, Ghana, Sierra Leone, Uganda), tropical America (Brazil, Cuba, French Guiana, Mexico, Nicaragua, Peru, Puerto Rico, St Croix), Australasia (Papua New Guinea), Asia (Malaysia, Singapore, Thailand) (Whalley et al., 1999 ) and North America (Calkins, 1886 ; Ellis & Everhart, 1888 ; Farr & Rossman, 2024 ; GBIF, 2024 ; MyCoPortal, 2024 ; O'Neal, 1914 ; Vasilyeva, Stephenson, & Miller, 2007 ). According to Vasilyeva et al.…”

Section: Canker Fungi and Other Fungi Associated With Sapwood ( ...mentioning

confidence: 99%

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Commodity risk assessment of maple veneer sheets from Canada

Bragard,

Baptista,

Chatzivassiliou

et al. 2024

EFS2

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The European Commission requested the EFSA Panel on Plant Health to deliver a risk assessment on the likelihood of pest freedom from Union quarantine pests and pests subject to measures adopted pursuant to Article 30 of Regulation (EU) No 2016/2031 for the maple veneer sheets manufactured according to the process set out by Canada, with emphasis on the freedom from Davidsoniella virescens and Phytophthora ramorum (non‐EU isolates). The assessment was conducted for veneer sheets of up to 0.7 mm and up to 6 mm thickness, taking into account the different phases in the veneer production in a systems approach. Some of those phases, taken alone, including the heat treatment of logs in a water bath, the cutting into thin veneer sheets and the final high heat drying of veneer sheets are expected to be effective against some of the pests, without uncertainties, making the system approach fully effective. The panel considers that no insects would survive cutting of logs into thin veneer sheets of 0.7 mm and that Xylella fastidiosa will not survive the temperatures in the water bath and final drying of veneers. The degree of pest freedom for the different groups of organisms is generally very high with slightly lower degree of pest freedom for veneer sheets of 6 mm thickness because of lower temperatures reached in the final drying of veneer sheets compared to thinner sheets. P. ramorum is not expected to survive the high heat drying of thin veneer sheets, but it may survive the lower temperatures inside thicker veneer sheets. The Expert Knowledge Elicitation (EKE) indicated, with 95% certainty, that between 9989 and 10,000 veneer sheets (thickness 6 mm) per 10,000 will be free from living P. ramorum. For D. virescens, the EKE indicated, with 95% certainty, that between 9984 and 10,000 veneer sheets (0.7 mm) per 10,000 and that between 9954 and 10,000 veneer sheets (6 mm) per 10,000 will be free from living inoculum. For other relevant groups of pests, the greatest likelihood of pest presence was observed for wood decay fungi. The EKE indicated, with 95% certainty, that between 9967 and 10,000 veneer sheets (0.7 mm) per 10,000 and that between 9911 and 10,000 veneer sheets (6 mm) per 10,000 will be free from living wood decay fungi.

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Xylariaceae on the Fringe

Chareprasert

Abdelghany

El-Sheikh

et al. 2011

Biology of Marine Fungi

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The Xylariaceae is one of the best-known pyrenomycete families (Ascomycota) and is distributed throughout the world. The majority are wood inhabitants and are prevalent in tropical and subtropical regions. Halorosellinia oceanicum is the most widely distributed in mangroves and can be regarded as truly manglicolous being frequently recorded as the dominant member of the family in such environments in S.E. Asia. In Malaysian mangroves, members of the Xylariaceae have been found to be numerically important with up to 9% present in one mangrove ecosystem. A further twelve xylariaceous genera are reported as occurring as their teleomorphs in mangrove forest and their immediate surroundings including Anthostomella, Astrocystis, Biscogniauxia, Camillea, Daldinia, Fasciatispora, Hypoxylon, Kretzschmaria, Nemania, Nipicola, Rosellinia and Xylaria. Furthermore, the presence of species from a number of these taxa, especially species of Anthostomella and Xylaria, are regularly isolated as endophytes from a variety of mangrove plant species. Mangrove Xylariaceae are also well known for their ability to produce novel and often bioactive metabolites.

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Camillea malaysianensis sp. nov. and the Distribution of Camillea in Southeast Asia

Cited by 9 publications

References 5 publications

Camillea (Xylariaceae, Ascomycota), including two new species, along a trans-Andean altitude gradient in Ecuador

Camillea (Xylariaceae, Ascomycota), including two new species, along a trans-Andean altitude gradient in Ecuador

Commodity risk assessment of maple veneer sheets from Canada

Xylariaceae on the Fringe

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