Yeasts from tropical forests: Biodiversity, ecological interactions, and as sources of bioinnovation.
biotechnological innovation
insects
plants
tropical forests
yeast biodiversity
Journal
Yeast (Chichester, England)
ISSN: 1097-0061
Titre abrégé: Yeast
Pays: England
ID NLM: 8607637
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
revised:
05
10
2023
received:
25
04
2023
accepted:
09
10
2023
medline:
8
11
2023
pubmed:
3
11
2023
entrez:
3
11
2023
Statut:
ppublish
Résumé
Tropical rainforests and related biomes are found in Asia, Australia, Africa, Central and South America, Mexico, and many Pacific Islands. These biomes encompass less than 20% of Earth's terrestrial area, may contain about 50% of the planet's biodiversity, and are endangered regions vulnerable to deforestation. Tropical rainforests have a great diversity of substrates that can be colonized by yeasts. These unicellular fungi contribute to the recycling of organic matter, may serve as a food source for other organisms, or have ecological interactions that benefit or harm plants, animals, and other fungi. In this review, we summarize the most important studies of yeast biodiversity carried out in these biomes, as well as new data, and discuss the ecology of yeast genera frequently isolated from tropical forests and the potential of these microorganisms as a source of bioinnovation. We show that tropical forest biomes represent a tremendous source of new yeast species. Although many studies, most using culture-dependent methods, have already been carried out in Central America, South America, and Asia, the tropical forest biomes of Africa and Australasia remain an underexplored source of novel yeasts. We hope that this review will encourage new researchers to study yeasts in unexplored tropical forest habitats.
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
511-539Subventions
Organisme : FCT/MCTES
Organisme : Natural Science and Engineering Research Council of Canada
Organisme : Fundação do Amparo a Pesquisa do EStado de Minas Gerais
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
Informations de copyright
© 2023 John Wiley & Sons Ltd.
Références
Aksornkoae, S. (1999). Mangrove: Ecology and Management. Kasetsart University Press.
Allard, S. M., Costa, M. T., Bulseco, A. N., Helfer, V., Wilkins, L. G. E., Hassenrück, C., Zengler, K., Zimmer, M., Erazo, N., Mazza Rodrigues, J. L., Duke, N., Melo, V. M. M., Vanwonterghem, I., Junca, H., Makonde, H. M., Jiménez, D. J., Tavares, T. C. L., Fusi, M., Daffonchio, D., … Bowman, J. (2020). Introducing the mangrove microbiome initiative: Identifying microbial research priorities and approaches to better understand, protect, and rehabilitate mangrove ecosystems. mSystems, 5(5):e00658-20. https://doi.org/10.1128/mSystems.00658-20
Alsammar, H., & Delneri, D. (2020). An update on the diversity, ecology and biogeography of the Saccharomyces genus. FEMS Yeast Research, 20, foaa013. https://doi.org/10.1093/femsyr/foaa013
Aravind, K., Naik, T. P., & Krishnaswamy, K. (2014). Exopolysaccharide production potential of yeast Cryptococcus flavescens SK01 strain from the phylloplane of Semecarpus kathalekanensis. Journal of Pure and Applied Microbiology, 8(4), 3339-3343.
Banin, L. F., Phillips, O. L., & Lewis, S. L. (2015). Tropical forests. In S. H. Kelvin, R. T. Corlett, & Y. Bergeron (Eds.), Routledge handbook of forest ecology (pp. 56-75). Routledge.
Barbosa, R., Almeida, P., Safar, S. V. B., Santos, R. O., Morais, P. B., Nielly-Thibault, L., Leducq, J.-B., Landry, C. R., Gonçalves, P., Rosa, C. A., & Sampaio, J. P. (2016). Evidence of natural hybridization in Brazilian wild lineages of Saccharomyces cerevisiae. Genome Biology and Evolution, 8, 317-329. https://doi.org/10.1093/gbe/evv263
Barbosa, R., Pontes, A., Santos, R. O., Montandon, G. G., de Ponzzes-Gomes, C. M., Morais, P. B., Gonçalves, P., Rosa, C. A., & Sampaio, J. P. (2018). Multiple rounds of artificial selection promote microbe secondary domestication-The case of Cachaça yeasts. Genome Biology and Evolution, 10(8), 1939-1955. https://doi.org/10.1093/gbe/evy132
Barriga, E. J. C., Barahona, P. P., Tufino, C., Bastidas, B., Guaman-Burneo, C., Freitas, L. F., & Rosa, C. A. (2014). An overview of the yeast biodiversity in the Galapagos islands and other Ecuadorian regions. In O. Grillo (Ed.), Biodiversity-The dynamic balance (pp. 193-232). IntechOpen. https://doi.org/10.5772/58303
Barros, K. O., Alvarenga, F. B. M., Magni, G., Souza, G. F. L., Abegg, M. A., Palladino, F., da Silva, S. S., Rodrigues, R. C. L. B., Sato, T. K., Hittinger, C. T., & Rosa, C. A. (2023). The Brazilian Amazonian rainforest harbors a high diversity of yeasts associated with rotting wood, including many candidates for new yeast species. Yeast, 40(2), 84-101. https://doi.org/10.1002/yea.3837
Barros, L. A., Mendonça, B. A. F., Sothe, C., Fernandes-Filho, E. I., & Elkin, C. (2021). Fire in the Atlantic Rainforest: An analysis of 20 years of fire foci distribution and their social-ecological drivers, Geocarto International 37(16), pp. 4737-4761. https://doi.org/10.1080/10106049.2021.1899301
Blackwell, M. (2017). Made for each other: Ascomycete yeasts and insects. Microbiology Spectrum, 5(3), FUNK-0081-2016. https://doi.org/10.1128/microbiolspec.FUNK-0081-2016
Boonmak, C., Khunnamwong, P., & Limtong, S. (2020). Yeast communities of primary and secondary peat swamp forests in Southern Thailand. Antonie Van Leeuwenhoek, 113, 55-69. https://doi.org/10.1007/s10482-019-01317-0
Boynton, P. J., Greig, D. (2014). The ecology and evolution of non-domesticated Saccharomyces species. Yeast, 31(12), 449-462. https://doi.org/10.1002/yea.3040
Buzzini, P., & Martini, A. (2002). Extracellular enzymatic activity profiles in yeast and yeast-like strains isolated from tropical environments. Journal of Applied Microbiology, 93(6), 1020-1025. https://doi.org/10.1046/j.1365-2672.2002.01783.x
Buzzini, P., Martini, A., Cappelli, F., Pagnoni, U. M., & Davoli, P. (2003). A study on volatile organic compounds (VOCs) produced by tropical ascomycetous yeasts. Antonie Van Leeuwenhoek, 84(4), 301-311. https://doi.org/10.1023/a:1026064527932
Buzzini, P., Vaughan, A. E., Turchetti, B., & Martini, A. (2004). La biodiversità dei lieviti isolati da ambienti tropicali: una fonte potenziale di molecole di interesse biotecnologico. Informatore Botanico Italiano, 36(1), 286-292.
Cadete, R. M., de Las Heras, A. M., Sandström, A. G., Ferreira, C., Gírio, F., Gorwa-Grauslund, M. F., Rosa, C. A., & Fonseca, C. (2016). Exploring xylose metabolism in Spathaspora species: XYL1.2 from Spathaspora passalidarum as the key for efficient anaerobic xylose fermentation in metabolic engineered Saccharomyces cerevisiae. Biotechnology for Biofuels, 9, 167. https://doi.org/10.1186/s13068-016-0570-6
Cadete, R. M., Melo, M. A., Dussán, K. J., Rodrigues, R. C. L. B., Silva, S. S., Zilli, J. E., Vital, M. J. S., Gomes, F. C. O., Lachance, M. A., & Rosa, C. A. (2012). Diversity and physiological characterization of d-xylose-fermenting yeasts isolated from the Brazilian Amazonian Forest. PLoS One, 7(8), e43135. https://doi.org/10.1371/journal.pone.0043135
Cadete, R. M., & Rosa, C. A. (2018). The yeasts of the genus Spathaspora: Potential candidates for second-generation biofuel production. Yeast, 35(2), 191-199. https://doi.org/10.1002/yea.3279
Cadete, R. M., Santos, R. O., Melo, M. A., Mouro, A., Gonçalves, D. L., Stambuk, B. U., Gomes, C. O., Lachance, M., & Rosa, C. A. (2009). Spathaspora arborariae sp. nov., a d-xylose-fermenting yeast species isolated from rotting wood in Brazil. FEMS Yeast Research, 9(8), 1338-1342. https://doi.org/10.1111/j.1567-1364.2009.00582.x
Canto, A., Herrera, C. M., & Rodriguez, R. (2017). Nectar living yeasts of a tropical host plant community: Diversity and effects on community wide floral nectar traits. PeerJ, 5, e3517. https://doi.org/10.7717/peerj.3517
Carvalho, F. P., de Souza, A. C., Magalhães-Guedes, K. T., Dias, D. R., Silva, C. F., & Schwan, R. F. (2013). Yeasts diversity in Brazilian Cerrado soils: Study of the enzymatic activities. African. Journal of Microbiology Research, 7(32), 4176-4190.
Chai, C. Y., Gao, W. L., Li, Y., Yan, Z. L., & Hui, F. L. (2022). Kodamaea hongheensis f.a., sp. nov., Kodamaea ovate f.a., sp. nov. and Kodamaea yamadae f.a., sp. nov., three new yeast species of Kodamaea (Saccharomycetales, Debaryomycetacae) from China. MycoKeys, 89, 89-137. https://doi.org/10.3897/mycokeys.89.81119
Chai, C.-Y., Gao, W.-L., Yan, Z.-L., & Hui, F.-L. (2022). Four new species of Trichomonascaceae (Saccharomycetales, Saccharomycetes) from Central China. MycoKeys, 90, 1-18.
Chai, C.-Y., Huang, L.-N., Cheng, H., Liu, W.-J., & Hui, F.-L. (2019). Wickerhamomyces menglaensis f.a., sp. nov., a yeast species isolated from rotten wood. International Journal of Systematic and Evolutionary Microbiology, 69, 1509-1514. https://doi.org/10.1099/ijsem.0.003350
Chimner, R. A., & Ewel, K. C. (2005). A tropical freshwater wetland: II. Production, decomposition, and peat formation. Wetlands Ecology and Management, 13, 671-684. https://doi.org/10.1007/s11273-005-0965-9
Chu, S.-B., Hu, W. T., & Hui, F. L. (2022). Torulaspora jiuxiensis sp. nov., a novel yeast species isolated from rotting wood. International Journal of Systematic and Evolutionary Microbiology, 72(12), 005629. https://doi.org/10.1099/ijsem.0.005629
Colvin, A. Z. (2018). Peripatric speciation. WikiJournal of Science, 1(2), 008.
Corte, L., Di Cagno, R., Groenewald, M., Roscini, L., Colabella, C., Gobbetti, M., & Cardinali, G. (2015). Phenotypic and molecular diversity of Meyerozyma guilliermondii strains isolated from food and other environmental niches, hints for an incipient speciation. Food Microbiology, 48, 206-215.
da Cunha, A. B., Shehata, A. M. E. T., & de Oliveira, W. (1957). A study of the diets and nutritional preferences of tropical species of Drosophila. Ecology, 38, 98-106.
Danforth, B. N., Minckley, R., & Neff, J. L. (2019). The solitary bees-Biology, evolution, conservation (p. 472). Princeton University Press.
David-Palma, M., Libkind, D., Brito, P. H., Silva, M., Bellora, N., Coelho, M. A., Heitman, J., Gonçalves, P., & Sampaio, J. P. (2020). The untapped Australasian diversity of astaxanthin-producing yeasts with biotechnological potential-Phaffia australis sp. nov. and Phaffia tasmanica sp. nov. Microorganisms, 8(11), 1651. https://doi.org/10.3390/microorganisms8111651
Deak, T. (2009). Ecology and biodiversity of yeasts with potential value in biotechnology. In T. Satyanarayna & G. Kunze (Eds.), Yeast biotechnology: Diversity and applications (pp. 151-168). Springer. https://doi.org/10.1007/978-1-4020-8292-4_8
Dedysh, S. N., Pankratov, T. A., Belova, S. E., Kulichevskaya, I. S., & Liesack, W. (2006). Phylogenetic analysis and in situ identification of bacteria community composition in an acidic Sphagnum peat bog. Applied and Environmental Microbiology, 72, 2110-2117. https://doi.org/10.1128/AEM.72.3.2110-2117.2006
Dinerstein, E., Olson, D., Joshi, A., Vynne, C., Burgess, N. D., Wikramanayake, E., Hahn, N., Palminteri, S., Hedao, P., Noss, R., Hansen, M., Locke, H., Ellis, E. C., Jones, B., Barber, C. V., Hayes, R., Kormos, C., Martin, V., Crist, E., … Saleem, M. (2017). An ecoregion-based approach to protecting half the terrestrial realm. BioScience, 67, 534-545.
Félix, C. R., Andrade, D. A., Almeida, J. H., Navarro, H. M. C., Fell, J. W., & Landell, M. F. (2020). Vishniacozyma alagoana sp. nov. a tremellomycetes yeast associated with plants from dry and rainfall tropical forests. International Journal of Systematic and Evolutionary Microbiology, 70(5), 3449-3454. https://doi.org/10.1099/ijsem.0.004193
Felix, C. R., Navarro, H. M. C., Paulino, G. V. B., Broetto, L., & Landell, M. F. (2017). Carlosrosaea hohenbergiae sp. nov. and Carlosrosaea aechmeae sp. nov., two tremellaceous yeasts isolated from bromeliads in north-eastern Brazil. International Journal of Systematic and Evolutionary Microbiology, 67(6), 1752-1757. https://doi.org/10.1099/ijsem.0.001856
Figueiredo, M. A., da Silva, T. H., Pinto, O. H. B., Leite, M. G. P., de Oliveira, F. S., Messias, M. C. T. B., Rosa, L. H., Câmara, P. E. A. S., Lopes, F. A. C., & Kozovits, A. R. (2023). Metabarcoding of soil fungal communities in rupestrian grassland areas preserved and degraded by mining: implications for restoration. Microbial Ecology, 85, 1045-1055. https://doi.org/10.1007/s00248-023-02177-y
Fleet, G. H. (2001). Biodiversity and ecology of Australasian yeasts (fungi). Australian Systematic Botany, 14(3), 501-511. https://doi.org/10.1071/SB00017
Freitas, L. F. D., Barriga, E. J. C., Barahona, P. P., Lachance, M. A., & Rosa, C. A. (2013). Kodamaea transpacifica f.a., sp. nov., a yeast species isolated from ephemeral flowers and insects in the Galápagos Islands and Malaysia: Further evidence for ancient human transpacific contacts. International Journal of Systematic and Evolutionary Microbiology, 63(11), 4324-4329. https://doi.org/10.1099/ijs.0.052282-0
Freitas, L. F. D., Batista, T. M., Santos, A. R. O., Hilário, H. O., Moreira, R. G., Franco, G. R., Morais, P. B., Lachance, M. A., & Rosa, C. A. (2020). Yeast communities associated with cacti in Brazil and the description of Kluyveromyces starmeri sp. nov. based on phylogenomic analyses. Yeast, 37(12): 625-637. https://doi.org/10.1002/yea.3528
Fungsin, B., Hamamoto, M., Arunpairojana, V., Sukhumavasi, J., Atthasampunna, P., & Nakase, T. (2001). Bensingtonia thailandica sp. nov., a novel basidiomycetous yeast species isolated from plant leaves in Thailand. International Journal of Systematic and Evolutionary Microbiology, 51, 1209-1213. https://doi.org/10.1099/00207713-51-3-1209
Fungsin, B., Hamamoto, M., Arunpairojana, V., Sukhumavasi, J., Atthasampunna, P., & Nakase, T. (2002). Kockovaella barringtoniae sp. nov., a new basidiomycetous yeast species isolated from a plant leaf collected in a tropical rain forest in Thailand. International Journal of Systematic and Evolutionary Microbiology, 52, 281-284. https://doi.org/10.1099/00207713-52-1-281
Fungsin, B., Takashima, M., Artjariyasripong, S., Arunpairojana, V., Hamamoto, M., & Nakase, T. (2002). Bullera arundinariae sp. nov., a new species of ballistoconidium-forming yeast isolated from a plant in Thailand. Microbiology and Culture Collections, 18(2), 83-90.
Fungsin, B., Takashima, M., Artjariyasripong, S., & Nakase, T. (2003). Bullera panici sp. nov. and Bullera siamensis sp. nov., two new yeasts in the Bullera variabilis cluster isolated in Thailand. Microbiology and Culture Collections, 19, 23-32.
Fungsin, B., Takashima, M., Artjariyasripong, S., Potacharoen, W., & Nakase, T. (2003). Bullera sakaeratica sp. nov., a new species of ballistoconidium-forming yeast found in Thailand. Microbiology and Culture Collections, 19, 33-39.
Fungsin, B., Takashima, M., Sugita, T., Artjariyasripong, S., Potacharoen, W., Tanticharoen, M., & Nakase, T. (2006). Bullera koratensis sp. nov. and Bullera lagerstroemiae sp. nov., two new ballistoconidium-forming yeast species in the Trichosporonales clade isolated from plant leaves in Thailand. The Journal of General and Applied Microbiology, 52(2), 73-81. https://doi.org/10.2323/jgam.52.73
Ganter, P. F. (2011). Everything is not everywhere: The distribution of cactophilic yeast. In D. Fontaneto (Ed.), Biogeography of microscopic organisms (pp. 130-176). Cambridge University Press. https://doi.org/10.1017/CBO9780511974878
Ganter, P. F., Morais, P. B., & Rosa, C. A. (2017). Yeasts in cacti and tropical fruit. In P. Buzzini, M. A. Lachance, & A. Yurkov (Eds.), Yeasts in natural ecosystems: Diversity. Springer. https://doi.org/10.1007/978-3-319-62683-3_8
Glover, T. (1878). Manuscript notes from my journal: Cotton, and the principal insects, &c., frequenting or injuring the plant, in the United States. U.S. Department of Agriculture, National Agricultural Library. https://doi.org/10.5962/t.171490
Glushakova, A., Maksimova, I., Morozova, A., & Kachalkin, A. (2019). Distribution features of yeasts in soils of South Vietnam (case study of the biogeocenoses of the National Park Cát Tiên). IOP Conference Series: Earth and Environmental Science, 368, 012012. https://doi.org/10.1088/1755-1315/368/1/012012
Gomes, F. C. O., Safar, S. V. B., Marques, A. R., Medeiros, A. O., Santos, A. R. O., Carvalho, C., Lachance, M. A., Sampaio, J. P., & Rosa, C. A. (2015). The diversity and extracellular enzymatic activities of yeasts isolated from water tanks of Vriesea minarum, an endangered bromeliad species in Brazil, and the description of Occultifur brasiliensis f.a., sp. nov. Antonie Van Leeuwenhoek, 107(2), 597-611. https://doi.org/10.1007/s10482-014-0356-4
Gomes, F. C. O., Safar, S. V. B., Santos, A. R. O., Lachance, M. A., & Rosa, C. A. (2016). Kockovaella libkindii sp. nov., a yeast species isolated from water tanks of bromeliad. International Journal of Systematic and Evolutionary Microbiology, 66(12), 5066-5069. https://doi.org/10.1099/ijsem.0.001471.t
Gonçalves, C., Coelho, M. A., Salema-Oom, M., & Gonçalves, P. (2016). Stepwise functional evolution in a fungal sugar transporter family. Molecular Biology and Evolution, 33(2), 352-366. https://doi.org/10.1093/molbev/msv220
Gonçalves, C., & Gonçalves, P. (2019). Multilayered horizontal operon transfers from bacteria reconstruct a thiamine salvage pathway in yeasts. Proceedings of the National Academy of Sciences of the United States of America,116(44), 22219-22228. https://doi.org/10.1073/pnas.1909844116.
Gonçalves, P., Gonçalves, C., Brito, P. H., & Sampaio, J. P. (2020). The Wickerhamiella/Starmerella clade-A treasure trove for the study of the evolution of yeast metabolism. Yeast, 37(4), 313-320. https://doi.org/10.1002/yea.3463
Gonçalves, P., Valério, E., Correia, C., de Almeida, J. M. G. C. F., & Sampaio, J. P. (2011). Evidence for divergent evolution of growth temperature preference in sympatric Saccharomyces species. PLoS One, 6, e20739. https://doi.org/10.1371/journal.pone.0020739
Gonçalves, C., Wisecaver, J. H., Kominek, J., Oom, M. S., Leandro, M. J., Shen, X. X., Opulente, D. A., Zhou, X., Peris, D., Kurtzman, C. P., Hittinger, C. T., Rokas, A., & Gonçalves, P. (2018). Evidence for loss and reacquisition of alcoholic fermentation in a fructophilic yeast lineage. eLife, 7, e33034. https://doi.org/10.7554/eLife.33034
Grondin, E., Shum Cheong Sing, A., Caro, Y., Raherimandimby, M., Randrianierenana, A. L., James, S., Nueno-Palop, C., François, J. M., & Petit, T. (2015). A comparative study on the potential of epiphytic yeasts isolated from tropical fruits to produce flavoring compounds. International Journal of Food Microbiology, 203, 101-108. https://doi.org/10.1016/j.ijfoodmicro.2015.02.032
Guamán-Burneo, M. C., Dussán, K. J., Cadete, R. M., Cheab, M. A. M., Portero, P., Carvajal-Barriga, E. J., da Silva, S. S., & Rosa, C. A. (2015). Xylitol production by yeasts isolated from rotting wood in the Galápagos Islands, Ecuador, and description of Cyberlindnera galapagoensis f.a., sp. nov. Antonie Van Leeuwenhoek, 108(4), 919-931. https://doi.org/10.1007/s10482-015-0546-8
Hadibarata, T., Khudhair, A. B., Kristanti, R. A., & Kamyab, H. (2017). Biodegradation of pyrene by Candida sp. S1 under high salinity conditions. Bioprocess and Biosystems Engineering, 40, 1411-1418. https://doi.org/10.1007/s00449-017-1798-7
Han, D. Y., Han, P. J., Rumbold, K., Koricha, A. D., Duan, S. F., Song, L., Shi, J. Y., Li, K., Wang, Q. M., & Bai, F. Y. (2021). Adaptive gene content and allele distribution variations in the wild and domesticated populations of Saccharomyces cerevisiae. Frontiers in Microbiology, 12, 247. https://doi.org/10.3389/FMICB.2021.631250/BIBTEX
He, P. Y., Shao, X. Q., Duan, S. F., Han, D. Y., Li, K., Shi, J. Y., Zhang, R. P., Han, P. J., Wang, Q. M., & Bai, F. Y. (2022). Highly diverged lineages of Saccharomyces paradoxus in temperate to subtropical climate zones in China. Yeast, 39, 69-82. https://doi.org/10.1002/YEA.3688
Hoang, N. T., & Kanemoto, K. (2021). Mapping the deforestation footprint of nations reveals growing threat to tropical forests. Nature Ecology & Evolution, 5(6), 845-853. https://doi.org/10.1038/s41559-021-01417-z.
Huang, L. N., Xi, Z. W., Li, Y., & Hui, F. L. (2018). Sugiyamaella xiaguanensis f.a., sp. nov., a yeast species isolated from rotting wood. International Journal of Systematic and Evolutionary Microbiology, 68(10), 3307-3310. https://doi.org/10.1099/ijsem.0.002988
Huang, L. N., Xi, Z. W., Zhai, Y. C., Chai, C. Y., & Hui, F. L. (2019). Saturnispora galanensis sp. nov., a yeast species isolated from rotting wood. International Journal of Systematic and Evolutionary Microbiology, 69(9), 2658-2661. https://doi.org/10.1099/ijsem.0.003501
Jacques, N., & Casaregola, S. (2019). Large biodiversity of yeasts in French Guiana and the description of Suhomyces coccinellae f.a. sp. nov. and Suhomyces faveliae f.a. sp. nov. International Journal of Systematic and Evolutionary Microbiology, 69(6), 1634-1649. https://doi.org/10.1099/ijsem.0.003369
Jadhav, R., Tiwari, S., Avchar, R., Groenewald, M., & Baghela, A. (2020). Suhomyces drosophilae sp. nov., isolated from Drosophila flies feeding on a stinkhorn mushroom. International Journal of Systematic and Evolutionary Microbiology, 70(9), 4908-4913. https://doi.org/10.1099/ijsem.0.004358
Jaiboon, K., Lertwattanasakul, N., Limtong, P., & Limtong, S. (2016). Yeasts from peat in a tropical peat swamp forest in Thailand and their ability to produce ethanol, indole-3-acetic acid and extracellular enzymes. Mycological Progress, 15, 755-770. https://doi.org/10.1007/s11557-016-1205-9
James, S. A., Barriga, E. J. C., Barahona, P. P., Harrington, T. C., Lee, C. F., Bond, C. J., & Roberts, I. N. (2014). Wickerhamomyces arborarius f.a., sp. nov., an ascomycetous yeast species found in arboreal habitats on three different continents. International Journal of Systematic and Evolutionary Microbiology, 64(Pt 3), 1057-1061. https://doi.org/10.1099/ijs.0.059162-0
James, S. A., Cadet, G. M., Carvajal Barriga, E. J., Barahona, P. P., Cross, K., Bond, C. J., & Roberts, I. N. (2011). Saturnispora quitensis sp. nov., a yeast species isolated from the Maquipucuna cloud forest reserve in Ecuador. International Journal of Systematic and Evolutionary Microbiology, 61(12), 3072-3076. https://doi.org/10.1099/ijs.0.030759-0
James, S. A., Carvajal Barriga, E. J., Barahona, P. P., Cross, K., Bond, C. J., & Roberts, I. N. (2013). Candida ecuadorensis sp. nov., an ascomycetous yeast species found in two separate regions of Ecuador. International Journal of Systematic and Evolutionary Microbiology, 63(Pt 1), 393-397. https://doi.org/10.1099/ijs.0.047555-0
James, S. A., Carvajal Barriga, E. J., Bond, C. J., Cross, K., Núñez, N. C., Portero, P. B., & Roberts, I. N. (2009). Candida carvajalis sp. nov., an ascomycetous yeast species from the Ecuadorian Amazon jungle. FEMS Yeast Research, 9(5), 784-788. https://doi.org/10.1111/j.1567-1364.2009.00518.x
James, S. A., Carvajal Barriga, E. J., Portero Barahona, P., Nueno-Palop, C., Cross, K., Bond, C. J., & Roberts, I. N. (2015). Kazachstania yasuniensis sp. nov., an ascomycetous yeast species found in mainland Ecuador and on the Galápagos. International Journal of Systematic and Evolutionary Microbiology, 65(4), 1304-1309. https://doi.org/10.1099/ijs.0.000102
Januário da Costa Neto, D., & Benevides de Morais, P. (2020). The vectoring of Starmerella species and other yeasts by stingless bees in a Neotropical savanna. Fungal Ecology, 47, 100973. https://doi.org/10.1016/j.funeco.2020.100973
Janzen, D. H. (1983). Hymenaea courbaril (Guapinol, Stinking Toe). In D. H. Janzen (Ed.), Costa Rican natural history (pp. 253-256). University of Chicago Press.
Janzen, D. H., & Hallwachs, W. (2009). Dynamic database for an inventory of the macrocaterpillar fauna, and its food plants and parasitoids, of Area de Conservacion Guanacaste (ACG), northwestern Costa Rica (nn-SRNP-nnnnn voucher codes). http://janzen.sas.upenn.edu
Kaewwichian, R., Khunnamwong, P., Jindamorakot, S., Lertwattanasakul, N., & Limtong, S. (2018). Cryptotrichosporon siamense sp. nov., a ballistoconidium-forming yeast species in Trichosporonales isolated in Thailand. International Journal of Systematic and Evolutionary Microbiology, 68, 2473-2477. https://doi.org/10.1099/ijsem.0.002858
Kanti, A. (2015). Carboxymethyl cellulose hydrolyzing yeast isolated from South East Sulawesi. Indonesia. Jurnal Biologi Indonesia, 11(2), 285-294.
Ke, T., Zhai, Y. C., Yan, Z. L., Hui, F. L. (2019). Kazachstania jinghongensis sp. nov. and Kazachstania menglunensis f.a., sp. nov., two yeast species isolated from rotting wood. International Journal of Systematic and Evolutionary Microbiology, 69(11): 3623-3628. https://doi.org/10.1099/ijsem.0.003670
Khamweera, P., Bamrong, N., & Pookmak, S. (2022). Identification of yeasts isolated from Khaoploung forest by comparative ITS and D1/D2 sequence analysis. Phranakhon Rajabhat Research Journal (Science and Technology), 17(1), 61-74.
Khunnamwong, P., Kingphadung, K., Lomthong, T., Kanpiengjai, A., Khanongnuch, C., & Limtong, S. (2022). Wickerhamiella nakhonpathomensis f.a. sp. nov., a novel ascomycetous yeast species isolated from a mushroom and a flower in Thailand. International Journal of Systematic and Evolutionary Microbiology, 72(1), 005191. https://doi.org/10.1099/ijsem.0.005191
Khunnamwong, P., Lertwattanasakul, N., & Limtong, S. (2020). Teunia siamensis f.a., sp. nov., a novel tremellaceous yeast species isolated from soil in a secondary peat swamp forest area. International Journal of Systematic and Evolutionary Microbiology, 70(6), 3673-3678. https://doi.org/10.1099/ijsem.0.004219
Khunnamwong, P., & Limtong, S. (2018). Saturnispora kantuleensis f.a., sp. nov., a novel yeast species isolated from peat in a tropical peat swamp forest in Thailand. International Journal of Systematic and Evolutionary Microbiology, 68(4), 1160-1164. https://doi.org/10.1099/ijsem.0.002641
Kleespies, R. G., Lim, Y. W., Tkaczuk, C., Wrzosek, M., Steinwender, B. M., & Wegensteiner, R. (2017). Metschnikowia cf. typographi and other pathogens from the bark beetle Ips sexdentatus-Prevalence, histological and ultrastructural evidence, and molecular characterization. Journal of Invertebrate Pathology, 143, 69-78.
Kobayashi, R., Kanti, A., & Kawasaki, H. (2017). Pichia chibodasensis sp. nov., isolated in Indonesia. International Journal of Systematic and Evolutionary Microbiology, 67(4), 1024-1027.
Kominek, J., Doering, D. T., Opulente, D. A., Shen, X. X., Zhou, X., DeVirgilio, J., Hulfachor, A. B., Groenewald, M., Mcgee, M. A., Karlen, S. D., Kurtzman, C. P., Rokas, A., & Hittinger, C. T. (2019). Eukaryotic acquisition of a bacterial operon. Cell, 176(6), 1356-1366.e10. https://doi.org/10.1016/j.cell.2019.01.034
Koricha, A. D., Han, D. Y., Bacha, K., & Bai, F. Y. (2019). Occurrence and molecular identification of wild yeasts from Jimma Zone, South West Ethiopia. Microorganisms, 7(12), 633. https://doi.org/10.3390/microorganisms7120633
Kurtzman, C. P., Robnett, C. J., Basehoar, E., & Ward, T. J. (2018). Four new species of Metschnikowia and the transfer of seven Candida species to Metschnikowia and Clavispora as new combinations. Antonie Van Leeuwenhoek, 111(11), 2017-2035. https://doi.org/10.1007/s10482-018-1095-8
Kurtzman, C. P., Robnett, C. J., & Blackwell, M. (2016). Description of Teunomyces gen. nov. for the Candida kruisii clade, Suhomyces gen. nov. for the Candida tanzawaensis clade and Suhomyces kilbournensis sp. nov. FEMS Yeast Research, 16(5), fow041. https://doi.org/10.1093/femsyr/fow041
Lachance, M. A. (2011a). Clavispora Rodrigues de Miranda (1979). In C. P. Kurtzman, J. W. Fell, & T. Boekhout (Eds.), The yeasts: A taxonomic study (5th ed., pp. 349-353). Elsevier.
Lachance, M. A. (2011b). Metschnikowia Kamienski (1899). In C. P. Kurtzman, J. W. Fell, & T. Boekhout (Eds.), The yeasts: A taxonomic study (5th ed., pp. 575-620). Elsevier.
Lachance, M. A. (2011c). Sporopachydermia Rodrigues de Miranda (1978). In C. P. Kurtzman, J. W. Fell, & T. Boekhout (Eds.), The yeasts: A taxonomic study (5th ed., pp. 799-803). Elsevier.
Lachance, M. A., Boekhout, T., Scorzetti, G., Fell, J. W., & Kurtzman, C. P. (2011). Candida Berkhout. In C. P. Kurtzman, J. W. Fell, & T. Boekhout (Eds.), The yeasts: A taxonomic study (5th ed., pp. 987-1277). Elsevier.
Lachance, M. A., Bowles, J. M., Mueller, C., & Starmer, W. T. (2000). On the biogeography of yeasts in the Wickerhamiella clade and description of Wickerhamiella lipophila sp. nov., the teleomorph of Candida lipophila. Canadian Journal of Microbiology, 46, 1145-1148.
Lachance, M. A., Dobson, J., Wijayanayaka, D. N., & Smith, A. M. E. (2010). The use of parsimony network analysis for the formal delineation of phylogenetic species of yeasts: Candida apicola, Candida azyma, and Candida parazyma sp. nov., cosmopolitan yeasts associated with floricolous insects. Antonie Van Leeuwenhoek, 97, 155-170.
Lachance, M. A., Ewing, C. P., Bowles, J. M., & Starmer, W. T. (2005). Metschnikowia hamakuensis sp. nov., Metschnikowia kamakouana sp. nov., and Metschnikowia mauinuiana sp. nov., three endemic yeasts from Hawaiian nitidulid beetles. International Journal of Systematic and Evolutionary Microbiology, 55, 1369-1377.
Lachance, M. A., Klemens, J. A., Bowles, J. M., & Janzen, D. H. (2001). The yeast community of sap fluxes of costa rican Maclura (Chlorophora) tinctoria and description of two new yeast species, Candida galis and Candida ortonii. FEMS Yeast Research, 1(2), 87-92.
Lachance, M. A., & Kurtzman, C. P. (2013). The yeast genus Tortispora gen. nov., description of Tortispora ganteri sp. nov., Tortispora mauiana fa, sp. nov., Tortispora agaves fa, sp. nov., Tortispora sangerardonensis fa, sp. nov., Tortispora cuajiniquilana fa, sp. nov., Tortispora starmeri fa, sp. nov. and Tortispora phaffii fa, sp. nov., reassignment of Candida caseinolytica to Tortispora caseinolytica fa, comb. nov., emendation of Botryozyma, and assignment of Botryozyma, Tortispora gen. nov. and Trigonopsis to the family Trigonopsidaceae fam. nov. International Journal of Systematic and Evolutionary Microbiology, 63(8), 3104-3114.
Lachance, M. A., Lawrie, D., Dobson, J., & Piggott, J. (2008). Biogeography and population structure of the neotropical endemic yeast species Metschnikowia lochheadii. Antonie Van Leeuwenhoek, 94, 403-414.
Lachance, M. A., Lee, D. K., & Hsiang, T. (2020). Delineating yeast species with genome average nucleotide identity: A calibration of ANI with haplontic, heterothallic Metschnikowia species. Antonie Van Leeuwenhoek, 113, 2097-2106.
Lachance M. A., Rosa C. A., Carvajal E. J., Freitas L. F. D., & Bowles J. M. (2012). Saccharomycopsis fodiens sp. nov., a rare preadacious yeast from three distant localities. International Journal of Systematic and Evolutionary Microbiology, 62(11), 2793-2798. https://doi.org/10.1099/ijs.0.043109-0
Lachance, M. A., Rosa, C. A., Starmer, W. T., Schlag Edler, B., Barker, J. S., & Bowles, J. M. (1998). Wickerhamiella australiensis, Wickerhamiella cacticola, Wickerhamiella occidentalis, Candida drosophilae, and Candida lipophila, five new related yeast species from flowers and associated insects. International Journal of Systematic Bacteriology, 48 Pt 4, 1431-1443.
Lachance, M. A., Starmer, W. T., & Phaff, H. J. (1990). Metschnikowia hawaiiensis sp. nov., a heterothallic haploid yeast from Hawaiian morning glory and associated drosophilids. International Journal of Systematic Bacteriology, 40, 415-420.
Lachance, M. A., Starmer, W. T., Rosa, C. A., Bowles, J. M., Barker, J. S. F., & Janzen, D. H. (2001). Biogeography of the yeasts of ephemeral flowers and their insects. FEMS Yeast Research, 1, 1-8.
Lachance, M. A., Vale, H. M. M., Sperandio, E. M., Carvalho, A. O. S., Santos, A. R. O., Grondin, C., Jacques, N., Casaregola, S., & Rosa, C. A. (2018). Wickerhamiella dianesei fa, sp. nov. and Wickerhamiella kurtzmanii fa, sp. nov., two yeast species isolated from plants and insects. International Journal of Systematic and Evolutionary Microbiology, 68(10), 3351-3355.
Lee, D. K., Hsiang, T., & Lachance, M. A. (2018). Metschnikowia mating genomics. Antonie Van Leeuwenhoek, 111(10), 1935-1953.
Lee, T. J., Liu, Y. C., Liu, W. A., Lin, Y. F., Lee, H. H., Ke, H. M., Huang, J. P., Lu, M. Y. J., Hsieh, C. L., Chung, K. F., Liti, G., & Tsai, I. J. (2022). Extensive sampling of Saccharomyces cerevisiae in Taiwan reveals ecology and evolution of predomesticated lineages. Genome Research, 32, 864-877. https://doi.org/10.1101/GR.276286.121
Lee, D. K., Santos, A. R. O., Hsiang, T., Rosa, C. A., & Lachance, M. A. (2020). Catching speciation in the act-act 2: Metschnikowia lacustris sp. nov., a sister species to Metschnikowia dekortorum. Antonie Van Leeuwenhoek, 113, 753-762.
Li, S., Youwei, C., Liyuan, Y., Aiqi, F., Lingqi, Z., Huiqiong, Y., & Wang, X. (2002). A study on yeasts of yunnan. I. Yeasts of tropical rain forest, Xishuangbanna. Journal of Yunnan University (Natural Sciences), 24(5), 378-380.
Li, A. H., Yuan, F. X., Groenewald, M., Bensch, K., Yurkov, A. M., Li, K., Han, P. J., Guo, L. D., Aime, M. C., Sampaio, J. P., Jindamorakot, S., Turchetti, B., Inacio, J., Fungsin, B., Wang, Q. M., & Bai, F. Y. (2020). Diversity and phylogeny of basidiomycetous yeasts from plant leaves and soil: Proposal of two new orders, three new families, eight new genera and one hundred and seven new species. Studies in Mycology, 96, 17-140. https://doi.org/10.1016/j.simyco.2020.01.002
Limtong, S., Am-In, S., Kaewwichian, R., Kaewkrajay, C., & Jindamorakot, S. (2020). Exploration of yeast communities in fresh coconut, palmyra, and nipa palm saps and ethanol-fermenting ability of isolated yeasts. Antonie Van Leeuwenhoek, 113, 2077-2095. https://doi.org/10.1007/S10482-020-01479-2/TABLES/5
Limtong, S., Imanishi, Y., Jindamorakot, S., Ninomiya, S., Yongmanitchai, W., & Nakase, T. (2008). Torulaspora maleeae sp. nov., a novel ascomycetous yeast species from Japan and Thailand. FEMS Yeast Research, 8, 337-343. https://doi.org/10.1111/j.1567-1364.2007.00324.x
Limtong, S., & Yongmanitchai, W. (2010). Candida chanthaburiensis sp. nov., Candida kungkrabaensis sp. nov. and Candida suratensis sp. nov., three novel yeast species from decaying plant materials submerged in water of mangrove forest. Antonie Van Leeuwenhoek, 98(3), 379-388. https://doi.org/10.1007/s10482-010-9451-3
Limtong, S., Yongmanitchai, W., Kawasaki, H., & Fujiyama, K. (2009). Wickerhamomyces edaphicus sp. nov. and Pichia jaroonii sp. nov., two ascomycetous yeast species isolated from forest soil in Thailand. FEMS Yeast Research, 9(3), 504-510. https://doi.org/10.1111/j.1567-1364.2009.00488.x
Limtong, S., Yongmanitchai, W., Tun, M. M., Kawasaki, H., & Seki, T. (2007). Kazachstania siamensis sp. nov., an ascomycetous yeast species from forest soil in Thailand. International Journal of Systematic and Evolutionary Microbiology, 57(2), 419-422. https://doi.org/10.1099/ijs.0.64539-0
Liti G. (2015). The fascinating and secret wild life of the budding yeast S. cerevisiae. Elife, 4, e05835. https://doi.org/10.7554/eLife.05835.001
Liu, W. Q., Han, P. J., Qiu, J. Z., & Wang, Q. M. (2012). Naumovozyma baii sp. nov., an ascomycetous yeast species isolated from rotten wood in a tropical forest. International Journal of Systematic and Evolutionary Microbiology, 62, 3095-3098. https://doi.org/10.1099/ijs.0.044909-0
Lopes, M. R., Ferreira, M. C., Carvalho, T. F. C., Pagnocca, F. C., Chagas, R. A., Morais, P. B., Rosa, L. H., Lachance, M. A., & Rosa, C. A. (2015). Yamadazyma riverae sp. nov., a yeast species isolated from plant materials. International Journal of Systematic and Evolutionary Microbiology, 65(12), 4469-4473.
Lopes, M. R., Lara, C. A., Moura, M. E. F., Uetanabaro, A. P. T., Morais, P. B., Vital, M. J. S., & Rosa, C. A. (2018). Characterisation of the diversity and physiology of cellobiose-fermenting yeasts isolated from rotting wood in Brazilian ecosystems. Fungal Biology, 122(7), 668-676. https://doi.org/10.1016/j.funbio.2018.03.008
Luong, D. T., Takashima, M., Ty, P. V., Dung, N. L., & Nakase, T. (2000). Four new species of Kockovaella isolated from plant leaves collected in Vietnam. The Journal of General and Applied Microbiology, 46(6), 297-310. https://doi.org/10.2323/jgam.46.297
Luong, D. T., Takashima, M., Ty, P. V., Dung, N. L., & Nakase, T. (2005). Bullera hoabinhensis sp. nov., a new ballistoconidiogenous yeast isolated from a plant leaf collected in Vietnam. The Journal of General and Applied Microbiology, 51(6), 335-342. https://doi.org/10.2323/jgam.51.335
Lüttge, U. (2008). Physiological ecology of tropical plants. Springer. https://doi.org/10.1007/978-3-540-71793-5
Lv, S. L., Chai, C. Y., Wang, Y., Yan, Z. L., & Hui, F. L. (2020). Five new additions to the genus Spathaspora (Saccharomycetales, Debaryomycetaceae) from southwest China. MycoKeys, 75, 31-49. https://doi.org/10.3897/mycokeys.75.57192
Marques, A. R., Resende, A. A., Gomes, F. C. O., Santos, A. R. O., Rosa, C. A., Duarte, A. A., de Lemos-Filho, J. P., & dos Santos, V. L. (2021). Plant growth-promoting traits of yeasts isolated from the tank bromeliad Vriesea minarum L.B. Smith and the effectiveness of Carlosrosaea vrieseae for promoting bromeliad growth. Brazilian Journal of Microbiology, 52(3), 1417-1429. https://doi.org/10.1007/s42770-021-00496-1
Matos, Í. T. S. R., de Souza, V. A., D'Angelo, G. R., Astolfi Filho, S., do Carmo, E. J., & Vital, M. J. S. (2021). Yeasts with fermentative potential associated with fruits of Camu-Camu (Myrciaria dubia, Kunth) from North of Brazilian Amazon. The Scientific World Journal, 2021, 1-6. https://doi.org/10.1155/2021/9929059
Maugeri, F., & Hernalsteens, S. (2007). Screening of yeast strains for transfructosylating activity. Journal of Molecular Catalysis B: Enzymatic, 49, 43-49. https://doi.org/10.1016/j.molcatb.2007.08.001
Melo, W. G. P., de Oliveira, T. B., Arcuri, S. L., de Morais, P. B., & Pagnocca, F. C. (2021). Yeasts in the nests of the leaf-cutter ant Acromyrmex balzani in a Savanna biome: exploitation of community and metabolic diversity. Antonie Van Leeuwenhoek, 114(6), 751-764. https://doi.org/10.1007/s10482-021-01555-1
Mok, W. Y., Luizão, R. C., do Socorro Barreto da Silva, M., Teixeira, M. F., & Muniz, E. G. (1984). Ecology of pathogenic yeasts in Amazonian soil. Applied and Environmental Microbiology, 47(2), 390-394.
Monteiro Moreira, G. A., & Martins do Vale, H. M. (2020). Soil yeast communities in revegetated post-mining and adjacent native areas in central Brazil. Microorganisms, 8(8), 1116. https://doi.org/10.3390/microorganisms8081116
Morais, C. G., Batista, T. M., Kominek, J., Borelli, B. M., Furtado, C., Moreira, R. G., Franco, G. R., Rosa, L. H., Fonseca, C., Hittinger, C. T., Lachance, M. A., & Rosa, C. A. (2017). Spathaspora boniae sp. nov., a d-xylose-fermenting species in the Candida albicans/Lodderomyces clade. International Journal of Systematic and Evolutionary Microbiology, 67(10), 3798-3805. https://doi.org/10.1099/ijsem.0.002186
Morais, C. G., Cadete, R. M., Uetanabaro, A. P. T., Rosa, L. H., Lachance, M. A., & Rosa, C. A. (2013). d-xylose-fermenting and xylanase-producing yeast species from rotting wood of two Atlantic Rainforest habitats in Brazil. Fungal Genetics and Biology, 60, 19-28. https://doi.org/10.1016/j.fgb.2013.07.003
Morais, P. B., Hagler, A. N., Rosa, C. A., Mendonca-Hagler, L. C., & Klaczko, L. B. (1992). Yeasts associated with Drosophila in tropical forests of Rio de Janeiro, Brazil. Canadian Journal of Microbiology, 38(11), 1150-1155. https://doi.org/10.1139/m92-188
Morais, P. B., Martins, M. B., Klaczko, L. B., Mendonça-Hagler, L. C., & Hagler, A. N. (1995). Yeast succession in the Amazon fruit Parahancornia amapa as resource partitioning among Drosophila spp. Applied and Environmental Microbiology, 61(12), 4251-4257. https://doi.org/10.1128/aem.61.12.4251-4257.1995
Morais, P. B., Pagnocca, F. C., & Rosa, C. A. (2006). Yeast communities in tropical rain forests in Brazil and other South American ecosystems. In C. A. Rosa & P. Gabor (Eds.), Biodiversity and ecophysiology of yeasts (pp. 461-484). Springer. https://doi.org/10.1007/3-540-30985-3_18
Morais, P. B., Rosa, C. A., & Hagler, A. N. (1995). Yeast communities as descriptors of habitat use by the Drosophila fasciola subgroup (repleta group) in Atlantic rain forests. Oecologia, 104(1), 45-51. https://doi.org/10.1007/BF00365561
Morais, C. G., Sena, L. M. F., Lopes, M. R., Santos, A. R. O., Barros, K. O., Alves, C. R., Uetanabaro, A. P. T., Lachance, M. A., & Rosa, C. A. (2020). Production of ethanol and xylanolytic enzymes by yeasts inhabiting rotting wood isolated in sugarcane bagasse hydrolysate. Fungal Biology, 124(7), 639-647. https://doi.org/10.1016/j.funbio.2020.03.005
Morais, P. B., Teixeira, L.C., Bowles, J. M., Lachance, M. A., & Rosa, C. A. (2005). Ogataea falcaomoraisii sp. nov., a sporogenous methylotrophic yeast from tree exudates. FEMS Yeast Research, 5(1). 81-85. https://doi.org/10.1016/j.femsyr.2004.05.006
Morais, P. B., de Sousa, F. M. P., & Rosa, C. A. (2020). Yeast in plant phytotelmata: Is there a “core” community in different localities of rupestrian savannas of Brazil? Brazilian Journal of Microbiology, 51(3), 1209-1218. https://doi.org/10.1007/s42770-020-00286-1
Morais, P., Teixeira, L., Bowles, J., Lachance, M., & Rosa, C. (2004). sp. nov., a sporogenous methylotrophic yeast from tree exudates. FEMS Yeast Research, 5(1), 81-85. https://doi.org/10.1016/j.femsyr.2004.05.006
Moreira, G. A. M., Pires, E. C. C., Barreto, C. C., & Vale, H. M. M. (2020). Total fungi and yeast distribution in soils over native and modified vegetation in central Brazil. Revista Brasileira de Ciência do Solo, 44, 1-19. https://doi.org/10.36783/18069657rbcs20200097
Morellato, L. P. C., & Haddad, C. F. B. (2000). Introduction: The Brazilian Atlantic Forest. Biotropica, 32, 786-792.
Mozzachiodi, S., Bai, F. Y., Baldrian, P., Bell, G., Boundy-Mills, K., Buzzini, P., Čadež, N., Cubillos, F. A., Dashko, S., Dimitrov, R., Fisher, K. J., Gibson, B., Gouliamova, D., Greig, D., Heistinger, L., Hittinger, C. T., Jecmenica, M., Koufopanou, V., Landry, C. R., … Boynton, P. (2022). Yeasts from temperate forests. Yeast, 39(1-2), 4-24. https://doi.org/10.1002/yea.3699
Murray, A. (1864). Monograph of the family Nitidulariae. Transactions of the Linneun Society, 24, 211-414.
Myers, N., Mittermeier, R. A., Mittermeier, C. G., da Fonseca, G. A. B., & Kent, J. (2000). Biodiversity hotspots for conservation priorities. Nature, 403(6772), 853-858. https://doi.org/10.1038/35002501
Nagahama, T. (2006). Yeast biodiversity in freshwater, marine and deep-sea environment. In C. A. Rosa & G. Peter (Eds.), The yeast handbook, biodiversity and ecophysiology of yeasts (pp. 241-262). Springer-Verlag.
Nakase, T., Jindamorakot, S., Am-In, S., Potacharoen, W., & Tanticharoen, M. (2006). Yeast biodiversity in tropical forests of Asia. In C. A. Rosa & P. Gabor (Eds.), Biodiversity and ecophysiology of yeasts (pp. 441-460). Springer. https://doi.org/10.1007/3-540-30985-3_17
Nakase, T., Jindamorakot, S., Ninomiya, S., Imanishi, Y., & Kawasaki, H. (2009). Candida wancherniae sp. nov. and Candida morakotiae sp. nov., two novel ascomycetous anamorphic yeast species found in Thailand. The Journal of General and Applied Microbiology, 55(2), 93-100.
Nasanit, R., Imklin, N., & Limtong, S. (2020). Assessment of yeasts in tropical peat swamp forests in Thailand. Mycological Progress, 19, 1559-1573. https://doi.org/10.1007/s11557-020-01646-9
Naumov, G. I., James, S. A., Naumova, E. S., Louis, E. J., & Roberts, I. N. (2000). Three new species in the Saccharomyces sensu stricto complex: Saccharomyces cariocanus, Saccharomyces kudriavzevii and Saccharomyces mikatae. International Journal of Systematic and Evolutionary Microbiology, 50, 1931-1942. https://doi.org/10.1099/00207713-50-5-1931/CITE/REFWORKS
Naumov, G. I., Lee, C.-F., & Naumova, E. S. (2013). Molecular genetic diversity of the Saccharomyces yeasts in Taiwan: Saccharomyces arboricola, Saccharomyces cerevisiae and Saccharomyces kudriavzevii. Antonie Van Leeuwenhoek, 103, 217-228. https://doi.org/10.1007/s10482-012-9803-2
Naumov, G. I., Naumova, E. S., Hagler, A. N., Mendonça-Hagler, L. C., & Louis, E. J. (1995). A new genetically isolated population of the Saccharomyces sensu stricto complex from Brazil. Antonie Van Leeuwenhoek, 67, 351-355. https://doi.org/10.1007/BF00872934/METRICS
Navarro, H. M. C., Félix, C. R., Tavares, V. D. F. S., de Sousa, F. M. P., Santos, A. R. O., Morais, P. B., Rosa, C. A., Valente, P., & Landell, M. F. (2022). Tremella ananatis sp. nov. and Tremella lamprococci sp. nov., two yeast species associated with bromeliads. International Journal of Systematic and Evolutionary Microbiology, 72(2), 005261. https://doi.org/10.1099/ijsem.0.005261
Neves, K. C. S., Porto, A. L. F., & Teixeira, M. F. S. (2006). Seleção de leveduras da Região Amazônica para produção de protease extracelular. Acta Amazonica, 36(3), 299-306. https://doi.org/10.1590/S0044-59672006000300002
Nitiyon, S., Khunnamwong, P., Lertwattanasakul, N., & Limtong, S. (2018). Candida kantuleensis sp. nov., a d-xylose-fermenting yeast species isolated from peat in a tropical peat swamp forest. International Journal of Systematic and Evolutionary Microbiology, 68, 2313-2318. https://doi.org/10.1099/ijsem.0.002835
Nwaefuna, A. E., Boekhout,T., Garcia-Aloy, M., Vrhovsek, U., & Zhou, N. (2023). Diversity of dung beetle-associated yeasts from pristine environments of Botswana. Yeast, 40(5-6), 182-196. https://doi.org/10.1002/yea.3852
Palilu, P. T., Kasiamdari, R. S., & Ilmi, M. (2019). Potential yeast from Indonesian wild forest honey showing ability to produce lipase for lipid transesterification. Microbiology and Biotechnology Letters, 47, 555-564. https://doi.org/10.4014/mbl.1907.07008
Paludo, C. R., Menezes, C., Silva-Junior, E. A., Vollet-Neto, A., Andrade-Dominguez, A., Pishchany, G., Khadempour, L., do Nascimento, F. S., Currie, C. R., Kolter, R., Clardy, J., & Pupo, M. T. (2018). Stingless bee larvae require fungal steroid to pupate. Scientific Reports, 8(1), 1122. https://doi.org/10.1038/s41598-018-19583-9
Paludo, C. R., Pishchany, G., Andrade-Dominguez, A., Silva-Junior, E. A., Menezes, C., Nascimento, F. S., Currie, C. R., Kolter, R., Clardy, J., & Pupo, M. T. (2019). Microbial community modulates growth of symbiotic fungus required for stingless bee metamorphosis. PLoS One, 14(7), e0219696. https://doi.org/10.1371/journal.pone.0219696
de Paula, G. T., Menezes, C., Pupo, M. T., & Rosa, C. A. (2021). Stingless bees and microbial interactions. Current Opinion in Insect Science, 44, 41-47. https://doi.org/10.1016/j.cois.2020.11.006
Pignal, L. C., & Lachaise, D. (1979). Les levures des drosophilidesde savanne d'Afrique intertropicale (Savannes de Lamto, C8te d'Ivoire). Mycopathologia, 68,155-165.
Pillay, R., Venter, M., Aragon-Osejo, J., González-del-Pliego, P., Hansen, A. J., Watson, J. E., & Venter, O. (2022). Tropical forests are home to over half of the world's vertebrate species. Frontiers in Ecology and the Environment, 20(1), 10-15. https://doi.org/10.1002/fee.2420
Pimenta, R. S., Alves, P. D. D., Almeida, G. M. F., Silva, J. F. M., Morais, P. B., Corrêa Jr., A., & Rosa, C. A. (2009). Yeast communities in two Atlantic Rain Forest fragments in Southeast Brazil. Brazilian Journal of Microbiology, 40(1), 90-95. https://doi.org/10.1590/S1517-838220090001000015
Polburee, P., Lertwattanasakul, N., Limtong, P., Groenewald, M., & Limtong, S. (2017). Nakazawaea todaengensis f.a., sp. nov., a yeast isolated from a peat swamp forest in Thailand. International Journal of Systematic and Evolutionary Microbiology, 67, 2377-2382. https://doi.org/10.1099/ijsem.0.001961
Pozo, M. I., van Kemenade, G., van Oystaeyen, A., Aledón-Catalá, T., Benavente, A., Van den Ende, W., Wäckers, F., & Jacquemyn, H. (2020). The impact of yeast presence in nectar on bumble bee behavior and fitness. Ecological Monographs, 90(1), e01393. https://doi.org/10.1002/ecm.1393
Rahbar Saadat, Y., Yari Khosroushahi, A., & Pourghassem Gargari, B. (2021). Yeast exopolysaccharides and their physiological functions. Folia Microbiologica, 66, 171-182. https://doi.org/10.1007/s12223-021-00856-2
dos Reis, J. B. A., do Vale, H. M. M., & Lorenzi, A. S. (2022). Insights into taxonomic diversity and bioprospecting potential of Cerrado endophytic fungi: A review exploring an unique Brazilian biome and methodological limitations. World Journal of Microbiology and Biotechnology, 38, 202.
Ren, Y., Chen, L., Niu, Q., & Hui, F. (2014). Description of Scheffersomyces henanensis sp. nov., a new d-xylose-fermenting yeast species isolated from rotten wood. PLoS One, 9(9), e92315.
Rezende, C. L., Scarano, F. R., Assad, E. D., Joly, C. A., Metzger, J. P., Strassburg, B. B. N., Tabarelli, M., Fonseca, G. A., & Mittermeier, R. A. (2018). From hotspot to hopespot: An opportunity for the Brazilian Atlantic Forest. Perspectives in Ecology and Conservation, 16(4), 208-214. https://doi.org/10.1016/j.pecon.2018.10.002
Robinson, H. A., Pinharanda, A., & Bensasson, D. (2016). Summer temperature can predict the distribution of wild yeast populations. Ecology and Evolution, 6, 1236-1250. https://doi.org/10.1002/ece3.1919
Rosa, C., Lachance, M., Silva, J., Teixeira, A., Marini, M., Antonini, Y., & Martins, R. (2003). Yeast communities associated with stingless bees. FEMS Yeast Research, 4(3), 271-275.
Rosa, C. A., Pagnocca, F. C., Lachance, M. A., Ruivo, C. C. C., Medeiros, A. O., Pimentel, M. R. C., Fontenelle, J. C. R., & Martins, R. P. (2007). Candida flosculorum sp. nov. and Candida floris sp. nov., two yeast species associated with tropical flowers. International Journal of Systematic and Evolutionary Microbiology, 57(12), 2970-2974.
Rosa, C. A., Viana, E. M., Martins, R. P., Antonini, Y., & Lachance, M. A. (1999). Candida batistae, a new yeast species associated with solitary digger nesting bees in Brazil. Mycologia, 91(3), 428-433.
Sachs, E. J., Abbas, H. K., Mengistu, A. (2006). First report of endophytic Candida ipomoeae isolated from ovules of upland cotton in Mississippi. Plant Disease, 90 (10), 1362. https://doi.org/10.1094/PD-90-1362B
Sampaio, P., & Gonçalves, P. (2008). Natural populations of Saccharomyces kudriavzevii in Portugal are associated with oak bark and are sympatric with S. cerevisiae and S. paradoxus. Applied and Environmental Microbiology, 74, 2144-2152. https://doi.org/10.1128/AEM.02396-07
Sampaio, J. P., & Gonçalves, P. (2017). Biogeography and ecology of the genus Saccharomyces. In P. Buzzini, M. A. Lachance, & A. Yurkov (Eds.), Yeasts in natural ecosystems: Ecology. Springer. https://doi.org/10.1007/978-3-319-61575-2_5
Santos, A. R. O., Aires, A., Pontes, A., Silva, M., Brito, P. H., Groenewald, M., Melo, C. G. S., Lachance, M. A., Sampaio, J. P., & Rosa, C. A. (2021). Phaffia brasiliana sp. nov., a yeast species isolated from soil in a Cerrado-Atlantic Rain Forest ecotone site in Brazil. International Journal of Systematic and Evolutionary Microbiology, 71(11), 005080. https://doi.org/10.1099/ijsem.0.005080
Santos, A. R. O., Lee, D. K., Ferreira, A. G., do Carmo, M. C., Rondelli, V. M., Barros, K. O., Hsiang, T., Rosa, C. A., & Lachance, M. A. (2020). The yeast community of Conotelus sp. (Coleoptera: Nitidulidae) in Brazilian passionfruit flowers (Passiflora edulis) and description of Metschnikowia amazonensis sp. nov., a large-spored clade yeast. Yeast, 37, 253-260.
Santos, A. R., Leon, M. P., Barros, K. O., Freitas, L. F. D., Hughes, A. F., Morais, P. B., Lachance, M. A., & Rosa, C. A. (2018). Starmerella camargoi fa, sp. nov., Starmerella ilheusensis fa, sp. nov., Starmerella litoralis fa, sp. nov., Starmerella opuntiae fa, sp. nov., Starmerella roubikii fa, sp. nov. and Starmerella vitae fa, sp. nov., isolated from flowers and bees, and transfer of related Candida species to the genus Starmerella as new combinations. International Journal of Systematic and Evolutionary Microbiology, 68(4), 1333-1343.
Santos, A. R. O., Perri, A. M., Andrietta, M. G. S., Rosa, C. A., & Lachance, M. A. (2015). The expanding large-spored Metschnikowia clade: Metschnikowia matae sp. nov., a yeast species with two varieties from the Brazilian Atlantic Forest. Antonie Van Leeuwenhoek, 108, 753-763.
Santos, A. R. O., Souza, G. F. L., Barros, K. O., Alvarenga, F. B. M., Lopes, M. R., Souza, L. M. D., Rosa, L. H., Góes-Neto, A., Morais, P. B., Lachance, M. A., & Rosa, C. A. (2023). Spathaspora brunopereirae sp. nov. and Spathaspora domphillipsii sp. nov., two d-xylose-fermenting ascosporogenous yeasts from Amazonian Forest biomes. International Journal of Systematic and Evolutionary Microbiology, 73(3), 005752. https://doi.org/10.1099/ijsem.0.005752
Sapsirisuk, S., Polburee, P., Lorliam, W., & Limtong, S. (2022). Discovery of oleaginous yeast from mountain forest soil in Thailand. Journal of Fungi, 8, 1100. https://doi.org/10.3390/jof8101100
Satianpakiranakorn, P., Khunnamwong, P., & Limtong, S. (2020). Yeast communities of secondary peat swamp forests in Thailand and their antagonistic activities against fungal pathogens cause of plant and postharvest fruit diseases. PLoS One, 15(3), e0230269. https://doi.org/10.1371/journal.pone.0230269
Sayer, J. A., Harcout, C. S., & Collins, N. M. (1992). The conservation Atlas of Tropical Forests: Africa. Macmillian Publishers Ltd.
Seike, T., Takekata, H., Uchida, Y., Sakata, N., Furusawa, C., & Matsuda, F. (2023). Wickerhamiella bidentis sp. nov., a novel yeast species isolated from flowers and insects in Japan. International Journal of Systematic and Evolutionary Microbiology, 73(3), 005739. https://doi.org/10.1099/ijsem.0.005739
Sena, L. M. F., Morais, C. G., Lopes, M. R., Santos, R. O., Uetanabaro, A. P. T., Morais, P. B., Vital, M. J. S., de Morais Jr., M. A., Lachance, M. A., & Rosa, C. A. (2017). d-xylose fermentation, xylitol production and xylanase activities by seven new species of Sugiyamaella. Antonie Van Leeuwenhoek, 110(1), 53-67. https://doi.org/10.1007/s10482-016-0775-5
Silva, J. M. C., Barbosa, L. C. F., Leal, I. R., & Tabarelli, M. (2017). The Caatinga: Understanding the challenges. In J. M. C. Silva, I. R. Leal, & M. Tabarelli (Eds.), Caatinga: The largest tropical dry forest region in South America (pp. 3-19). Springer.
Silva, J. L. S., Cruz-Neto, O., Peres, C. A., Tabarelli, M., & Lopes, A. V. (2019). Climate change will reduce suitable Caatinga dry forest habitat for endemic plants with disproportionate impacts on specialized reproductive strategies. PLoS One, 14(5), e0217028. https://doi.org/10.1371/journal.pone.0217028
Sipiczki, M. (2022). Taxonomic revision of the pulcherrima clade of Metschnikowia (fungi): Merger of species. Taxonomy, 2(1), 107-123.
Sipiczki, M., Pfliegler, W. P., Safar, S. V. B., Morais, P. B., & Rosa, C. A. (2016). Metahyphopichia laotica gen. nov., sp. nov., a polymorphic yeast related to Hyphopichia. International Journal of Systematic and Evolutionary Microbiology, 66(7), 2550-2557. https://doi.org/10.1099/ijsem.0.001091
van der Sluis, C., Tramper, J., & Wijffels, R. H. (2001). Enhancing and accelerating flavour formation by salt-tolerant yeasts in Japanese soy-sauce processes. Trends in Food Science & Technology, 12(9), 322-327. https://doi.org/10.1016/S0924-2244(01)00094-2
Smith, M. T., & Groenewald, M. (2012). The treasure trove of yeast genera and species described by Johannes van der Walt (1925-2011). IMA Fungus, 3(2), 179-187. https://doi.org/10.5598/imafungus.2012.03.02.10
Sniegowski, P., Dombrowski, P., & Fingerman, E. (2002). and coexist in a natural woodland site in North America and display different levels of reproductive isolation from European conspecifics. FEMS Yeast Research, 1, 299-306. https://doi.org/10.1016/S1567-1356(01)00043-5
Souza, G. F. L., Barros, K. O., Alvarenga, F. B. M., Santos, A. R. O., Fonseca, C. R. V., Abegg, M. A., Lachance, M. A., & Rosa, C. A. (2023). Sugiyamaella bielyi f. a., sp. nov. and Sugiyamaella amazoniana f. a., sp. nov., two yeast species isolated from passalid beetles and rotting wood in Amazonia. International Journal of Systematic and Evolutionary Microbiology, 73(4), 005839. https://doi.org/10.1099/ijsem.0.005839
Souza, G. F. L., Valentim, L. T. C. N., Nogueira, S. R., & Abegg, M. (2017). Efficient production of second generation etanoland xylitol by yeasts from Amazonian beetles (Coleopter) and their galleries. African Journal of Microbiology Research, 11(20), 814-824. https://doi.org/10.5897/AJMR2017.8522
Souza Jr., C. M., Z. Shimbo, J., Rosa, M. R., Parente, L. L., A. Alencar, A., Rudorff, B., Hasenack, H., Matsumoto, M., G. Ferreira, L., Souza-Filho, P., de Oliveira, S. W., Rocha, W. F., Fonseca, A. V., Marques, C. B., Diniz, C. G., Costa, D., Monteiro, D., Rosa, E. R., Vélez-Martin, E., … Azevedo, T. (2020). Reconstructing three decades of land use and land cover changes in Brazilian biomes with landsat archive and earth engine. Remote Sensing, 12(17), 2735. https://doi.org/10.3390/rs12172735
Sperandio, E. M., Martins do Vale, H. M., & Moreira, G. A. M. (2015). Yeasts from native Brazilian Cerrado plants: Occurrence, diversity and use in the biocontrol of citrus green mould. Fungal Biology, 119(11), 984-993. https://doi.org/10.1016/j.funbio.2015.06.011
Stevens, G. (1983). Bursera simaruba (Indio desnudo, jiñocuave, gumbo limbo). In D. H. Janzen (Ed.), Costa Rican natural history (pp. 2201-2202). University of Chicago Press.
Sudbery, P. E. (2011). Growth of Candida albicans hyphae. Nature Reviews Microbiology, 9(10), 737-748.
Suh, S. O., Nguyen, N. H., & Blackwell, M. (2005). Nine new Candida species near C. membranifaciens isolated from insects. Mycological Research, 109(9), 1045-1056.
Surussawadee, J., Jindamorakot, S., Nakase, T., Lee, C. F., & Limtong, S. (2015). Hannaellaphyllophila sp. nov., a basidiomycetous yeast species associated with plants in Thailand. International Journalof Systematic and Evolutionary Microbiology, 65(7), 2135-2140. https://doi.org/10.1099/ijs.0.000231
Sweeney, J., Kuehne, H., & Sniegowski, P. (2004). Sympatric natural and populations have different thermal growth profiles. FEMS Yeast Research, 4, 521-525. https://doi.org/10.1016/S1567-1356(03)00171-5
Teixeira, A. C. P., Marini, M. M., Nicoli, J. R., Antonini, Y., Martins, R. P., Lachance, M. A., & Rosa, C. A. (2003). Starmerella meliponinorum sp. nov., a novel ascomycetous yeast species associated with stingless bees. International Journal of Systematic and Evolutionary Microbiology, 53(1), 339-343.
Teixeira, M. G., Venticinque, E. M., Lion, M. B., & Pinto, M. P. (2021). The Brazilian Caatinga protected areas: An extremely unbalanced conservation system. Environmental Conservation, 48(4), 287-294. https://doi.org/10.1017/S0376892921000308
Thanh, V. N. (2006). Lipomyces orientalis sp. nov., a yeast species isolated from soil in Vietnam. International Journal of Systematic and Evolutionary Microbiology, 56, 2009-2013. https://doi.org/10.1099/ijs.0.64241-0
Thongekkaew, J., Khumsap, A., & Chatsa-nga, P. (2012). Yeasts in mixed deciduous forest areas of Phujong Nayoy National Park and their ability to produce xylanase and carboxymethyl cellulase. Songklanakarin Journal of Science and Technology, 34(2), 157-163.
Tiago, M. R. M., Cortez, A. C. A., Souza, J. V. B., Brito, D. V., & Carvalho-Zilse, G. A. (2022). Fungi associated with hives and castes of the Amazonian stingless bees Melipona interrupta and Melipona seminigra. Research Square. https://doi.org/10.21203/rs.3.rs-2355604/v1
Trochine, A., Turchetti, B., Vaz, A. B. M., Brandao, L., Rosa, L. H., Buzzini, P., Rosa, C., & Libkind, D. (2017). Description of Dioszegia patagonica sp. nov., a novel carotenogenic yeast isolated from cold environments. International Journal of Systematic and Evolutionary Microbiology, 67(11), 4332-4339. https://doi.org/10.1099/ijsem.0.002211
Urbina, H., Schuster, J., & Blackwell, M. (2013). The gut of Guatemalan passalid beetles: A habitat colonized by cellobiose and xylose-fermenting yeasts. Fungal Ecology, 6(5), 339-355. https://doi.org/10.1016/j.funeco.2013.06.005
Vale, S. C. S., Guimarães, A. P. M., & Morais, P. B. (2015). Occurrence andbiotechnological potential of yeasts associated with almond fruits of Attalea speciosa Mart ex Spreng. Journalof Bioenergy and Food Science, 2 (4),1-5. https://doi.org/10.18067/jbfs.v2i4
de Vega, C., Albaladejo, R. G., Guzmán, B., Steenhuisen, S. L., Johnson, S. D., Herrera, C. M., & Lachance, M. A. (2017). Flowers as a reservoir of yeast diversity: Description of Wickerhamiella nectarea f.a. sp. nov., and Wickerhamiella natalensis f.a. sp. nov. from South African flowers and pollinators, and transfer of related Candida species to the genus Wickerhamiella as new combinations. FEMS Yeast Research, 17(5), fox054. https://doi.org/10.1093/femsyr/fox054
de Vega, C., Guzmán, B., Lachance, M. A., Steenhuisen, S. L., Johnson, S. D., & Herrera, C. M. (2012). Metschnikowia proteae sp. nov., a nectarivorous insect-associated yeast species from Africa. International Journal of Systematic and Evolutionary Microbiology, 62, 2538-2545.
de Vega, C., Guzmán, B., Steenhuisen, S. L., Johnson, S. D., Herrera, C. M., & Lachance, M. A. (2014). Metschnikowia drakensbergensis sp. nov. and Metschnikowia caudata sp. nov., endemic yeasts associated with Protea flowers in South Africa. International Journal of Systematic and Evolutionary Microbiology, 64, 3724-3732.
Vital, M. J. S., Abranches, J., Hagler, A. N., & Mendonça-Hagler, L. C. (2001). Mycocinogenic yeasts isolated from Amazon soils of the Maracá Ecological Station, Roraima-Brazil. Brazilian Journal of Microbiology, 33, 217-223.
Wang, S. A., Jia, J. H., & Bai, F. Y. (2008). Candida alocasiicola sp. nov., Candida hainanensis sp. nov., Candida heveicola sp. nov. and Candida musiphila sp. nov., novel anamorphic, ascomycetous yeast species isolated from plants. Antonie Van Leeuwenhoek, 94, 257-265. https://doi.org/10.1007/s10482-008-9238-y
Wang, Q.-M., Liu, W.-Q., Liti, G., Wang, S.-A., & Bai, F.-Y. (2012). Surprisingly diverged populations of Saccharomyces cerevisiae in natural environments remote from human activity. Molecular Ecology, 21, 5404-5417. https://doi.org/10.1111/j.1365-294X.2012.05732.x
Wang, J., Zhao, M., Xie, N., Huang, M., & Feng, Y. (2022). Community structure of yeast in fermented soy sauce and screening of functional yeast with potential to enhance the soy sauce flavor. International Journal of Food Microbiology, 370, 109652. https://doi.org/10.1016/j.ijfoodmicro.2022.109652
Wardlaw, A. M., Berkers, T. E., Man, K. C., & Lachance, M. A. (2009). Population structure of two beetle-associated yeasts: Comparison of a New World asexual and an endemic Nearctic sexual species in the Metschnikowia clade. Antonie Van Leeuwenhoek, 96, 1-15.
Wiens, F., Zitzmann, A., Lachance, M.-A., Yegles, M., Pragst, F., Wurst, F. M., von Holst, D., Guan, S. L., & Spanagel, R. (2008). Chronic intake of fermented floral nectar by wild treeshrews. Proceedings of the National Academy of Sciences of the United States of America, 105, 10426-10431. https://doi.org/10.1073/pnas.0801628105
Zhai, Y. C., Huang, L. N., Xi, Z. W., Chai, C. Y., & Hui, F. L. (2019). Candida yunnanensis sp. nov. and Candida parablackwelliae sp. nov., two yeast species in the Candida albicans/Lodderomyces clade. International Journal of Systematic and Evolutionary Microbiology, 69(9), 2775-2780. https://doi.org/10.1099/ijsem.0.003552
Zheng, J., Liu, K.-F., Liu, Z-J, Zhang, L., & Hui, F.-L. (2017). Deakozyma yunnanensis sp. nov., a novel yeast species isolated from rotten wood. International Journal of Systematic and Evolutionary Microbiology, 67(7), 2436-2439. https://doi.org/10.1099/ijsem.0.001978
Zong, L. (2020). The path to effective national park conservation and management: Hainan Tropical Rainforest National Park System Pilot Area. International Journal of Geoheritage and Parks, 8(4), 225-229. https://doi.org/10.1016/j.ijgeop.2020.11.009