Achala Rathnayaka

Ms. Achala Rathnayaka

School of Science, Mae Fah Luang University, Chiang Rai, Thailand
orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 July 2024 in New Zealand Journal of Botany
Verified
Journal Article
Closed access
ARAchala Rathnayaka
Achala Rathnayaka
Danushka Sandaruwan TennakoonDanushka Sandaruwan Tennakoon
Danushka Sandaruwan Tennakoon
GJGareth E.B. Evan Benjamin Jones
Gareth E.B. Evan Benjamin Jones
Dhanushka Nadeeshan WanasingheDhanushka Nadeeshan Wanasinghe
Dhanushka Nadeeshan Wanasinghe
DBD. Jayarama Bhat
D. Jayarama Bhat
Samantha C. KarunarathnaSamantha C. Karunarathna
Samantha C. Karunarathna

10 July 2024 in Nature
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Journal Article
Open access
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NANerea Abrego
Nerea Abrego
BFBrendan Furneaux
Brendan Furneaux
BHBess Hardwick
Bess Hardwick
PSPanu Somervuo
Panu Somervuo
IPIsabella Palorinne
Isabella Palorinne
OOOtso Ovaskainen
Otso Ovaskainen
Fungi are among the most diverse and ecologically important kingdoms in life. However, the distributional ranges of fungi remain largely unknown as do the ecological mechanisms that shape their distributions1,2. To provide an integrated view of the spatial and seasonal dynamics of fungi, we implemented a globally distributed standardized aerial sampling of fungal spores3. The vast majority of operational taxonomic units were detected within only one climatic zone, and the spatiotemporal patterns of species richness and community composition were mostly explained by annual mean air temperature. Tropical regions hosted the highest fungal diversity except for lichenized, ericoid mycorrhizal and ectomycorrhizal fungi, which reached their peak diversity in temperate regions. The sensitivity in climatic responses was associated with phylogenetic relatedness, suggesting that large-scale distributions of some fungal groups are partially constrained by their ancestral niche. There was a strong phylogenetic signal in seasonal sensitivity, suggesting that some groups of fungi have retained their ancestral trait of sporulating for only a short period. Overall, our results show that the hyperdiverse kingdom of fungi follows globally highly predictable spatial and temporal dynamics, with seasonality in both species richness and community composition increasing with latitude. Our study reports patterns resembling those described for other major groups of organisms, thus making a major contribution to the long-standing debate on whether organisms with a microbial lifestyle follow the global biodiversity paradigms known for macroorganisms4,5.

17 February 2022 in Fungal Diversity
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Journal Article
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ISIndunil Senanayake
Indunil Senanayake
DPDhandevi Pem
Dhandevi Pem
ARAchala Rathnayaka
Achala Rathnayaka
NANuwanthika Wijesinghe Arachchige
Nuwanthika Wijesinghe Arachchige
Saowaluck TibprommaSaowaluck Tibpromma
Saowaluck Tibpromma
NXNing Xie
Ning Xie
Sexual reproduction is the basic way to form high genetic diversity and it is beneficial in evolution and speciation of fungi. The global diversity of teleomorphic species in Ascomycota has not been estimated. This paper estimates the species number for sexual ascomycetes based on five different estimation approaches, viz. by numbers of described fungi, by fungus:substrate ratio, by ecological distribution, by meta-DNA barcoding or culture-independent studies and by previous estimates of species in Ascomycota. The assumptions were made with the currently most accepted, “2.2–3.8 million” species estimate and results of previous studies concluding that 90% of the described ascomycetes reproduce sexually. The Catalogue of Life, Species Fungorum and published research were used for data procurement. The average value of teleomorphic species in Ascomycota from all methods is 1.86 million, ranging from 1.37 to 2.56 million. However, only around 83,000 teleomorphic species have been described in Ascomycota and deposited in data repositories. The ratio between described teleomorphic ascomycetes to predicted teleomorphic ascomycetes is 1:22. Therefore, where are the undiscovered teleomorphic ascomycetes? The undescribed species are no doubt to be found in biodiversity hot spots, poorly-studied areas and species complexes. Other poorly studied niches include extremophiles, lichenicolous fungi, human pathogens, marine fungi, and fungicolous fungi. Undescribed species are present in unexamined collections in specimen repositories or incompletely described earlier species. Nomenclatural issues, such as the use of separate names for teleomorph and anamorphs, synonyms, conspecific names, illegitimate and invalid names also affect the number of described species. Interspecies introgression results in new species, while species numbers are reduced by extinctions.

14 September 2022 in Phytotaxa
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Journal Article
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ARAchala Rathnayaka
Achala Rathnayaka
TWThilini Chethana Kandawatte Wedaralalage
Thilini Chethana Kandawatte Wedaralalage
APAlan Phillips
Alan Phillips
GJGareth E.B. Evan Benjamin Jones
Gareth E.B. Evan Benjamin Jones
Botryosphaeriaceae is the largest family in Botryosphaeriales, consisting of 22 genera. The family is worldwide in distribution and occurs on a wide variety of plant hosts. Botryosphaeriaceae includes endophytic, saprobic, and plant pathogenic species associated with canker and die-back diseases, most common on woody plants. The present study establishes two novel species of Dothiorella and new host and geographical records for species of Botryosphaeria, Dothiorella, Neodeightonia, and Sphaeropsis. Taxa were identified based on morphology coupled with phylogenetic analyses based on maximum likelihood and Bayesian analyses of SSU, LSU, ITS, tef1-α and β-tub sequences. The taxa are described and illustrated.

29 January 2023 in Journal of Fungi
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Journal Article
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ARAchala Rathnayaka
Achala Rathnayaka
TWThilini Chethana Kandawatte Wedaralalage
Thilini Chethana Kandawatte Wedaralalage
APAlan Phillips
Alan Phillips
Jian-Kui LiuJian-Kui Liu
Jian-Kui Liu
Milan C. SamarakoonMilan C. Samarakoon
Milan C. Samarakoon
CHANG-LIN ZHAOCHANG-LIN ZHAO
CHANG-LIN ZHAO
Botryosphaeriales (Dothideomycetes, Ascomycota) occur in a wide range of habitats as endophytes, saprobes, and pathogens. The order Botryosphaeriales has not been subjected to evaluation since 2019 by Phillips and co-authors using phylogenetic and evolutionary analyses. Subsequently, many studies introduced novel taxa into the order and revised several families separately. In addition, no ancestral character studies have been conducted for this order. Therefore, in this study, we re-evaluated the character evolution and taxonomic placements of Botryosphaeriales species based on ancestral character evolution, divergence time estimation, and phylogenetic relationships, including all the novel taxa that have been introduced so far. Maximum likelihood, maximum parsimony, and Bayesian inference analyses were conducted on a combined LSU and ITS sequence alignment. Ancestral state reconstruction was carried out for conidial colour, septation, and nutritional mode. Divergence times estimates revealed that Botryosphaeriales originated around 109 Mya in the early epoch of the Cretaceous period. All six families in Botryosphaeriales evolved in the late epoch of the Cretaceous period (66–100 Mya), during which Angiosperms also appeared, rapidly diversified and became dominant on land. Families of Botryosphaeriales diversified during the Paleogene and Neogene periods in the Cenozoic era. The order comprises the families Aplosporellaceae, Botryosphaeriaceae, Melanopsaceae, Phyllostictaceae, Planistromellaceae and Saccharataceae. Furthermore, current study assessed two hypotheses; the first one being “All Botryosphaeriales species originated as endophytes and then switched into saprobes when their hosts died or into pathogens when their hosts were under stress”; the second hypothesis states that “There is a link between the conidial colour and nutritional mode in botryosphaerialean taxa”. Ancestral state reconstruction and nutritional mode analyses revealed a pathogenic/saprobic nutritional mode as the ancestral character. However, we could not provide strong evidence for the first hypothesis mainly due to the significantly low number of studies reporting the endophytic botryosphaerialean taxa. Results also showed that hyaline and aseptate conidia were ancestral characters in Botryosphaeriales and supported the relationship between conidial pigmentation and the pathogenicity of Botryosphaeriales species.

30 May 2024 in Scientific Data
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Journal Article
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OOOtso Ovaskainen
Otso Ovaskainen
NANerea Abrego
Nerea Abrego
BFBrendan Furneaux
Brendan Furneaux
BHBess Hardwick
Bess Hardwick
PSPanu Somervuo
Panu Somervuo
TRTomas Roslin
Tomas Roslin
Novel methods for sampling and characterizing biodiversity hold great promise for re-evaluating patterns of life across the planet. The sampling of airborne spores with a cyclone sampler, and the sequencing of their DNA, have been suggested as an efficient and well-calibrated tool for surveying fungal diversity across various environments. Here we present data originating from the Global Spore Sampling Project, comprising 2,768 samples collected during two years at 47 outdoor locations across the world. Each sample represents fungal DNA extracted from 24 m3 of air. We applied a conservative bioinformatics pipeline that filtered out sequences that did not show strong evidence of representing a fungal species. The pipeline yielded 27,954 species-level operational taxonomic units (OTUs). Each OTU is accompanied by a probabilistic taxonomic classification, validated through comparison with expert evaluations. To examine the potential of the data for ecological analyses, we partitioned the variation in species distributions into spatial and seasonal components, showing a strong effect of the annual mean temperature on community composition.