PDF (Español)
FLIP
How to Cite
Moscote-Velasquez, C. E. (2026). Biodiversity of macrofungi: a scientometric review Camilo Enrique Moscote-Velasquez . Biosalud, 20(1). https://doi.org/10.17151/biosa.2021.20.1.4
More Citation Formats
Authors
Abstract
Introduction: Fungi hold enormous potential across various industries, including the food, medical, and biotechnology sectors, and are particularly notable for their applications in the production of antibiotics, enzymes, and fermented foods. Their vast diversity suggests applications in various branches of the biological sciences, ranging from biodegradation to bioremediation. Although these organisms have significant scientific and social importance, studies in Colombia that adopt a scientometric approach to analyze their biological diversity remain scarce. Methodology: This study conducts a scientometric review of fungal biodiversity at the global level, with a supplementary section highlighting some studies conducted in Colombia. Results: Three main approaches were identified: global fungal diversity, the adaptive capacity of fungi to adverse environmental conditions, and their application in innovative industries such as biotechnology. Furthermore, the importance of strengthening mycological research in key ecosystems, such as tropical dry forests and northern Colombia, which harbor a wealth of species not yet documented, is emphasized. Conclusions: It is proposed that researchers design action plans aimed at prioritizing studies according to local and international needs, thereby maximizing the scientific and social impact of their research.
References
1. Niskanen T, Lücking R, Dahlberg A, Gaya E, Suz L, Mikryukov V, et al. Pushing the Frontiers of Biodiversity Research: Unveiling the Global Diversity, Distribution, and Conservation of Fungi [Internet]. Annu Rev Environ Resour. 2023;48. Available from: http://dx.doi.org/10.1146/annurev-environ-112621-090937
2. Grzesiak B, Węgrzyn MH, Turowska A, Twarużek M. Macrofungal sporocarp community in the lichen Scots pine forests. Open Life Sci. 2024;19(1):20220973. https://doi.org/10.1515/biol-2022-0973
3. Falandysz J. Mercury bio-extraction by fungus Coprinus comatus: a possible bioindicator and mycoremediator of polluted soils? Environ Sci Pollut Res Int. 2016; 23:7444-7451. https://doi.org/10.1007/s11356-015-5971-8
4. Hyde K, Xu J, Rapior S, Jeewon R, Lumyong S, Niego AGT, et al. The amazing potential of fungi: 50 ways we can exploit fungi industrially. Fungal Divers. 2019;97(1):1-136. https://hal.umontpellier.fr/hal-02196145v1/file/Hyde2019_fungaldiversity_1.pdf
5. Hawksworth DL, Lücking R. Fungal Diversity Revisited: 2.2 to 3.8 Million Species. Microbiol Spectr. 2017;5(4). https://doi.org/10.1128/microbiolspec.funk-0052-2016
6. Royal Botanic Gardens, Kew. Kew Research Repository [Internet]. London: Royal Botanic Gardens, Kew; 2021. Available from: https://kew.iro.bl.uk/
7. Gómez-Montoya N, Ríos Sarmiento C, Zora-Vergara B, Benjumea-Aristizabal C, Santa-Santa DJ, Zuluaga-Moreno M, et al. Diversidad de macrohongos (Basidiomycota) de Colombia: Listado de especies [Internet]. Actual Biol. 2022;44(116). Available from: https://revistas.udea.edu.co/index.php/actbio/article/view/346103
8. Urina-Triana MA, Piñeres-Melo MA, Mantilla-Morrón M, Butt-Aziz S, Galeano-Muñoz L, Naz S, et al. Machine learning and AI approaches for analyzing diabetic and hypertensive retinopathy in ocular images: A literature review. IEEE Access. 2024;12:54590-607. Available from: https://ieeexplore.ieee.org/stamp/stamp.jsp?arnumber=10474002
9. Vargas-Hernández A, Robledo S, Quiceno GR. Virtual teaching for online learning from the perspective of higher education: A bibliometric analysis. J Sci Res. 2024;13(2):406-418. Available from: https://pdfs.semanticscholar.org/a2fe/63efc4e1c6fd8ace494d9cf249190d974267.pdf
10. Robledo S, Valencia L, Zuluaga M, Arbelaez Echeverri O, Arboleda Valencia JW. Tosr: Create the Tree of Science from WoS and Scopus. J Sci Res. 2024;13(2):459-65. https://pdfs.semanticscholar.org/ab4b/8e23053bd5e61ccfe442ef722a7f95c263b0.pdf
11. Bornmann L, Leydesdorff L. Scientometrics in a changing research landscape: bibliometrics has become an integral part of research quality evaluation and has been changing the practice of research. EMBO Rep. 2014;15(12):1228-32. https://doi.org/10.15252/embr.201439608
12. Zuluaga M, Robledo S, Arbelaez-Echeverri O, Osorio-Zuluaga GA, Duque-Méndez N. Tree of Science - ToS: A web-based tool for scientific literature recommendation. Search less, research more! [Internet]. Issu Sci Technol Libr. 2022;(100). Available from: https://journals.library.ualberta.ca/istl/index.php/istl/article/view/2696
13. Tedersoo L, Mett M, Ishida TA, Bahram M. Phylogenetic relationships among host plants explain differences in fungal species richness and community composition in ectomycorrhizal symbiosis. New Phytol. 2013;199(3):822-31. Available from: https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.12328
14. van der Wal A, Geydan TD, Kuyper TW, de Boer W. A thready affair: linking fungal diversity and community dynamics to terrestrial decomposition processes. FEMS Microbiol Rev. 2013;37(4):477-94. https://doi.org/10.1111/1574-6976.12001
15. Saldarriaga-Hernández S, Velasco-Ayala C, Leal-Isla Flores P, de Jesús Rostro-Alanis M, Parra-Saldivar R, Iqbal HMN, et al. Biotransformation of lignocellulosic biomass into industrially relevant products with the aid of fungi-derived lignocellulolytic enzymes. Int J Biol Macromol. 2020;161:1099-116. https://doi.org/10.1016/j.ijbiomac.2020.06.047
16. Raynaud M, Goutaudier V, Louis K, Al-Awadhi S, Dubourg Q, Truchot A, et al. Impact of the COVID-19 pandemic on publication dynamics and non-COVID-19 research production. BMC Med Res Methodol. 2021;21(255). https://doi.org/10.1186/s12874-021-01404-9
17. Riccaboni M, Verginer L. The impact of the COVID-19 pandemic on scientific research in the life sciences. PLoS One. 2022;17(2):e0263001. https://doi.org/10.1371/journal.pone.0263001
18. Pasdaran A, Zare M, Hamedi A, Hamedi A. A Review of the Chemistry and Biological Activities of Natural Colorants, Dyes, and Pigments: Challenges, and Opportunities for Food, Cosmetics, and Pharmaceutical Application. Chem Biodivers. 2023;20(8):e202300561. https://doi.org/10.1002/cbdv.202300561
19. Taylor DL, Bhatnagar JM. Fungi in soil: a rich community with diverse functions. In: Soil Microbiology, Ecology and Biochemistry. Elsevier; 2024. p. 75–129. https://doi.org/10.1016/B978-0-12-822941-5.00004-1
20. Pecoraro L, Angelini P, Arcangeli A, Bistocchi G, Gargano ML, La Rosa A, et al. Macrofungi in Mediterranean maquis along seashore and altitudinal transects. Plant Biosyst. 2014;148(2):367-76. https://doi.org/10.1080/11263504.2013.877535
21. Boddy L, Büntgen U, Egli S, Gange AC, Heegaard E, Kirk PM, et al. Climate variation effects on fungal fruiting. Fungal Ecol. 2014;10:20-33. https://doi.org/10.1016/j.funeco.2013.10.006
22. Jaklitsch WM, Stadler M, Voglmayr H. Blue pigment in Hypocrea caerulescens sp. nov. and two additional new species in sect. Trichoderma. Mycologia. 2012;104(4):925-941.
23. Lackner G, Misiek M, Braesel J, Hoffmeister D. Genome mining reveals the evolutionary origin and biosynthetic potential of basidiomycete polyketide synthases. Fungal Genet Biol. 2012;49(12):996-1003. https://doi.org/10.1016/j.fgb.2012.09.009
24. Kaya A, Uzun Y, Karacan İH, Yakar S. Contributions to Turkish Pyronemataceae from Gaziantep province. Turk J Botany. 2016;40:298-307. https://doi.org/10.3906/bot-1508-4
25. Vizzini A, Clericuzio M, Boccardo F, Ercole E. A new Cortinarius of section Calochroi (Basidiomycota, Agaricomycetes) from Mediterranean Quercus woodlands (Italy). Mycologia. 2012;104(6):1502-9.
26. Singer R. Agaricales in Modern Taxonomy. Königstein: Koeltz Scientific Books; 1986.
27. White TJ, Bruns T, Lee SB, Taylor JW. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, editors. PCR protocols: a guide to methods and applications. New York: Academic Press; 1990. p. 315-322.
28. Gardes M, Bruns TD. ITS primers with enhanced specificity for basidiomycetes--application to the identification of mycorrhizae and rusts. Mol Ecol. 1993;2(2):113–8. https://doi.org/10.1111/j.1365-294x.1993.tb00005.x
29. CABI. Fungal biodiversity. Wallingford (UK): CAB International; 2003. Available from: https://www.cabidigitallibrary.org/doi/book/10.1079/9780851998268.0000
30. Knudsen H, Vesterholt J., editors. Funga Nordica: agaricoid, boletoid and cyphelloid genera. Nordsvamp; 2008.
31. Smith JE. Mycorrhizal symbiosis (third edition). Soil Sci Soc Am J. 2009;73(2):694-694. https://doi.org/10.2136/sssaj2008.0015br
32. Tedersoo L, May TW, Smith ME. Ectomycorrhizal lifestyle in fungi: global diversity, distribution, and evolution of phylogenetic lineages. Mycorrhiza. 2010;20(4):217-63.
33. O’Hanlon R, Harrington TJ. The macrofungal diversity and community of Atlantic oak (Quercus petraea and Q. Robur) forests in Ireland. An. Jard. Bot. Madr. 2012;69(1):107-17. Available from: https://www.redalyc.org/pdf/556/55624809006.pdf
34. Abrego N, Bässler C, Christensen M, Heilmann-Clausen J. Implications of reserve size and forest connectivity for the conservation of wood-inhabiting fungi in Europe. Biol Conserv. 2015;191:469-77. https://ui.adsabs.harvard.edu/link_gateway/2015BCons.191..469A/doi:10.1016/j.biocon.2015.07.005
35. Akata I, Uzun Y, Kaya A. Macromycetes determined in Yomra (Trabzon) district. Turk J Botany. 2014;38(5):999-1012. https://doi.org/10.3906/BOT-1309-22
36. Solak MH, Alli H, Işiloğlu M, Güngör H, Kalmiş E. Contributions to the macrofungal diversity of Antalya Province. Turk J Botany. 2014;38(2):386-97. https://doi.org/10.3906/bot-1302-15
37. Kaya A. Contributions to the macrofungal diversity of Atatürk Dam Lake basin. Turk J Botany. 2015;39(1):162-72. https://doi.org/10.3906/bot-1404-70
38. Shiryaev AG, Zmitrovich IV, Ezhov ON. Taxonomic and Ecological Structure of Basidial Macromycetes Biota in Polar Deserts of the Northern Hemisphere. Contemp. Probl. Ecol. 2018;11(5):458-71. https://doi.org/10.1134/S1995425518050086
39. Uzun Y, Kaya A. New additions to Turkish Pezizales from the Eastern black sea region. Turk J Botany. 2019;43(2):262-70. https://doi.org/10.3906/bot-1802-34
40. Uzun Y, Kaya A. First records of Hydnobolites and Pachyphlodes species from Turkey. Mycotaxon. 2018;133(3):415-21. https://doi.org/10.5248/133.415
41. Shakhova N, Volobuev S. Cultural and enzymatic activity studies of a pathogenic wood-decaying fungus Fomitiporia hippophaeicola (Hymenochaetales, Basidiomycota), recollected in the Eastern Caucasus. Arch Microbiol. 2023;205(249). https://doi.org/10.1007/s00203-023-03587-9?urlappend=%3Futm_source%3Dresearchgate.net%26utm_medium%3Darticle
42. Smith AH, Theirs HD. A contribution toward a monograph of North American species of Suillus. Ann Arbor (MI): privately published; 1964 [cited 2024 Nov]. Available from: https://research.fs.usda.gov/treesearch/49006
43. Wagg C, Bender SF, Widmer F, van der Heijden MGA. Soil biodiversity and soil community composition determine ecosystem multifunctionality. Proc Natl Acad Sci U S A. 2014;111(14):5266-70. https://doi.org/10.1073/pnas.1320054111
44. Piepenbring M. Introducción a la micología en los trópicos. St. Paul (MN): The American Phytopathological Society; 2015. Available from: https://doi.org/10.1094/9780890546147.fm
45. Dorjey K, Kumar S, Sharma YP. The adaptations of high-altitude mushrooms in the cold desert of Ladakh. In: Advances in Asian Human-Environmental Research. Cham: Springer Nature Switzerland; 2023. p. 95–110.
46. Peng Z, Wei S, Hu Y, Qi B, Yuan C, Wang Q, et al. Assessment of Fungal Diversity in Minqin County, a Typical Arid Region in Northwestern China. Curr Microbiol. 2023;80(62). https://doi.org/10.1007/s00284-022-03167-y
47. Vašutová M, Vítovcová K, Manukjanová A, Prach K. Fungal troublemakers – using indicator species with ephemeral fruitbodies to evaluate recovery of formerly extracted raised bogs. Ecol Indic. 2023;154(110574):110574. https://doi.org/10.1016/j.ecolind.2023.110574
48. Stierle AA, Stierle DB. Bioactive Secondary Metabolites Produced by the Fungal Endophytes of Conifers. Natural product communications [Internet]. 2015;10(10):1671-82. Available from: https://pubmed.ncbi.nlm.nih.gov/26669101/
49. Vasco-Palacios AM, Franco-Molano AE, López-Quintero CA, Boekhout T. Biota Colombiana [Internet]. Biota. 2005;6(1). [cited 2024 Nov 24]. Available from: https://revistas.humboldt.org.co/index.php/biota/article/view/153
50. López-Quintero CA, Straatsma G, Franco-Molano AE, Boekhout T. Macrofungal diversity in Colombian Amazon forests varies with regions and regimes of disturbance. Biodivers. Conserv. 2012;21(9):2221–43.
51. Vasco-Palacios AM, Molano AEF. Diversity of Colombian macrofungi (Ascomycota - Basidiomycota) [Internet]. Medellín (Colombia): Universidad de Antioquia; 2019. Available from: https://ipt.biodiversidad.co/sib/resource?r=udea_mhongos_literatura_001
52. da Marcela Vasco-Palacios A, López-Quintero C, Franco-Molano AE, Boekhout T. Austroboletus amazonicus sp. nov. and Fistulinella campinaranae var. scrobiculata, two commonly occurring boletes from a forest dominated by Pseudomonotes tropenbosii (Dipterocarpaceae) in Colombian Amazonia. Mycologia. 2014;106(5):1004-14. https://doi.org/10.3852/13-324
53. Vargas N, Gonçalves SC, Franco-Molano AE, Restrepo S, Pringle A. In Colombia the Eurasian fungus is expanding its range into native, tropical forests. Mycologia. 2019;111(5):758-71. https://doi.org/10.1080/00275514.2019.1636608
54. Royal Botanic Gardens, Kew. Catalogue of Fungi of Colombia [Internet]. 2022 [cited 2024 Nov 24]. Available from: http://kew.iro.bl.uk/downloads/3ff2c9cb-c057-48a8-8b4f-ab516279dcbf
55. Charria-Girón E, Vasco-Palacios AM, Moncada B, Marin-Felix Y. Colombian fungal diversity: Untapped potential for diverse applications. Microbiol Res (Pavia). 2023;14(4):2000–21. https://doi.org/10.3390/microbiolres14040135
56. Aqueveque P, Anke T, Anke H, Sterner O, Becerra J, Silva M. Favolon B, a new triterpenoid isolated from the Chilean Mycena sp. strain 96180. J Antibiot (Tokyo). 2005;58(1):61-4. https://doi.org/10.1038/ja.2005.7
57. Castañeda-Ramírez G, Aguilar-Marcelino L, López-Guillen G. Macroscopic and microscopic fungi with insecticidal activity. Chil J Agric Res. 2022;82(2):348-57. http://dx.doi.org/10.4067/S0718-58392022000200348
58. Rakshith D, Gurudatt DM, Yashavantha Rao HC, Chandra Mohana N, Nuthan BR, Ramesha KP, et al. Bioactivity-guided isolation of antimicrobial metabolite from Xylaria sp [Internet]. Process Biochem. 2020; Available from: https://linkinghub.elsevier.com/retrieve/pii/S1359511319315570
59. Stoyanova K, Gerginova M, Peneva N, Dincheva I, Alexieva Z. Biodegradation and utilization of the pesticides glyphosate and carbofuran by two yeast strains. Processes (Basel). 2023;11(12):3343. https://doi.org/10.3390/pr11123343
2. Grzesiak B, Węgrzyn MH, Turowska A, Twarużek M. Macrofungal sporocarp community in the lichen Scots pine forests. Open Life Sci. 2024;19(1):20220973. https://doi.org/10.1515/biol-2022-0973
3. Falandysz J. Mercury bio-extraction by fungus Coprinus comatus: a possible bioindicator and mycoremediator of polluted soils? Environ Sci Pollut Res Int. 2016; 23:7444-7451. https://doi.org/10.1007/s11356-015-5971-8
4. Hyde K, Xu J, Rapior S, Jeewon R, Lumyong S, Niego AGT, et al. The amazing potential of fungi: 50 ways we can exploit fungi industrially. Fungal Divers. 2019;97(1):1-136. https://hal.umontpellier.fr/hal-02196145v1/file/Hyde2019_fungaldiversity_1.pdf
5. Hawksworth DL, Lücking R. Fungal Diversity Revisited: 2.2 to 3.8 Million Species. Microbiol Spectr. 2017;5(4). https://doi.org/10.1128/microbiolspec.funk-0052-2016
6. Royal Botanic Gardens, Kew. Kew Research Repository [Internet]. London: Royal Botanic Gardens, Kew; 2021. Available from: https://kew.iro.bl.uk/
7. Gómez-Montoya N, Ríos Sarmiento C, Zora-Vergara B, Benjumea-Aristizabal C, Santa-Santa DJ, Zuluaga-Moreno M, et al. Diversidad de macrohongos (Basidiomycota) de Colombia: Listado de especies [Internet]. Actual Biol. 2022;44(116). Available from: https://revistas.udea.edu.co/index.php/actbio/article/view/346103
8. Urina-Triana MA, Piñeres-Melo MA, Mantilla-Morrón M, Butt-Aziz S, Galeano-Muñoz L, Naz S, et al. Machine learning and AI approaches for analyzing diabetic and hypertensive retinopathy in ocular images: A literature review. IEEE Access. 2024;12:54590-607. Available from: https://ieeexplore.ieee.org/stamp/stamp.jsp?arnumber=10474002
9. Vargas-Hernández A, Robledo S, Quiceno GR. Virtual teaching for online learning from the perspective of higher education: A bibliometric analysis. J Sci Res. 2024;13(2):406-418. Available from: https://pdfs.semanticscholar.org/a2fe/63efc4e1c6fd8ace494d9cf249190d974267.pdf
10. Robledo S, Valencia L, Zuluaga M, Arbelaez Echeverri O, Arboleda Valencia JW. Tosr: Create the Tree of Science from WoS and Scopus. J Sci Res. 2024;13(2):459-65. https://pdfs.semanticscholar.org/ab4b/8e23053bd5e61ccfe442ef722a7f95c263b0.pdf
11. Bornmann L, Leydesdorff L. Scientometrics in a changing research landscape: bibliometrics has become an integral part of research quality evaluation and has been changing the practice of research. EMBO Rep. 2014;15(12):1228-32. https://doi.org/10.15252/embr.201439608
12. Zuluaga M, Robledo S, Arbelaez-Echeverri O, Osorio-Zuluaga GA, Duque-Méndez N. Tree of Science - ToS: A web-based tool for scientific literature recommendation. Search less, research more! [Internet]. Issu Sci Technol Libr. 2022;(100). Available from: https://journals.library.ualberta.ca/istl/index.php/istl/article/view/2696
13. Tedersoo L, Mett M, Ishida TA, Bahram M. Phylogenetic relationships among host plants explain differences in fungal species richness and community composition in ectomycorrhizal symbiosis. New Phytol. 2013;199(3):822-31. Available from: https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.12328
14. van der Wal A, Geydan TD, Kuyper TW, de Boer W. A thready affair: linking fungal diversity and community dynamics to terrestrial decomposition processes. FEMS Microbiol Rev. 2013;37(4):477-94. https://doi.org/10.1111/1574-6976.12001
15. Saldarriaga-Hernández S, Velasco-Ayala C, Leal-Isla Flores P, de Jesús Rostro-Alanis M, Parra-Saldivar R, Iqbal HMN, et al. Biotransformation of lignocellulosic biomass into industrially relevant products with the aid of fungi-derived lignocellulolytic enzymes. Int J Biol Macromol. 2020;161:1099-116. https://doi.org/10.1016/j.ijbiomac.2020.06.047
16. Raynaud M, Goutaudier V, Louis K, Al-Awadhi S, Dubourg Q, Truchot A, et al. Impact of the COVID-19 pandemic on publication dynamics and non-COVID-19 research production. BMC Med Res Methodol. 2021;21(255). https://doi.org/10.1186/s12874-021-01404-9
17. Riccaboni M, Verginer L. The impact of the COVID-19 pandemic on scientific research in the life sciences. PLoS One. 2022;17(2):e0263001. https://doi.org/10.1371/journal.pone.0263001
18. Pasdaran A, Zare M, Hamedi A, Hamedi A. A Review of the Chemistry and Biological Activities of Natural Colorants, Dyes, and Pigments: Challenges, and Opportunities for Food, Cosmetics, and Pharmaceutical Application. Chem Biodivers. 2023;20(8):e202300561. https://doi.org/10.1002/cbdv.202300561
19. Taylor DL, Bhatnagar JM. Fungi in soil: a rich community with diverse functions. In: Soil Microbiology, Ecology and Biochemistry. Elsevier; 2024. p. 75–129. https://doi.org/10.1016/B978-0-12-822941-5.00004-1
20. Pecoraro L, Angelini P, Arcangeli A, Bistocchi G, Gargano ML, La Rosa A, et al. Macrofungi in Mediterranean maquis along seashore and altitudinal transects. Plant Biosyst. 2014;148(2):367-76. https://doi.org/10.1080/11263504.2013.877535
21. Boddy L, Büntgen U, Egli S, Gange AC, Heegaard E, Kirk PM, et al. Climate variation effects on fungal fruiting. Fungal Ecol. 2014;10:20-33. https://doi.org/10.1016/j.funeco.2013.10.006
22. Jaklitsch WM, Stadler M, Voglmayr H. Blue pigment in Hypocrea caerulescens sp. nov. and two additional new species in sect. Trichoderma. Mycologia. 2012;104(4):925-941.
23. Lackner G, Misiek M, Braesel J, Hoffmeister D. Genome mining reveals the evolutionary origin and biosynthetic potential of basidiomycete polyketide synthases. Fungal Genet Biol. 2012;49(12):996-1003. https://doi.org/10.1016/j.fgb.2012.09.009
24. Kaya A, Uzun Y, Karacan İH, Yakar S. Contributions to Turkish Pyronemataceae from Gaziantep province. Turk J Botany. 2016;40:298-307. https://doi.org/10.3906/bot-1508-4
25. Vizzini A, Clericuzio M, Boccardo F, Ercole E. A new Cortinarius of section Calochroi (Basidiomycota, Agaricomycetes) from Mediterranean Quercus woodlands (Italy). Mycologia. 2012;104(6):1502-9.
26. Singer R. Agaricales in Modern Taxonomy. Königstein: Koeltz Scientific Books; 1986.
27. White TJ, Bruns T, Lee SB, Taylor JW. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, editors. PCR protocols: a guide to methods and applications. New York: Academic Press; 1990. p. 315-322.
28. Gardes M, Bruns TD. ITS primers with enhanced specificity for basidiomycetes--application to the identification of mycorrhizae and rusts. Mol Ecol. 1993;2(2):113–8. https://doi.org/10.1111/j.1365-294x.1993.tb00005.x
29. CABI. Fungal biodiversity. Wallingford (UK): CAB International; 2003. Available from: https://www.cabidigitallibrary.org/doi/book/10.1079/9780851998268.0000
30. Knudsen H, Vesterholt J., editors. Funga Nordica: agaricoid, boletoid and cyphelloid genera. Nordsvamp; 2008.
31. Smith JE. Mycorrhizal symbiosis (third edition). Soil Sci Soc Am J. 2009;73(2):694-694. https://doi.org/10.2136/sssaj2008.0015br
32. Tedersoo L, May TW, Smith ME. Ectomycorrhizal lifestyle in fungi: global diversity, distribution, and evolution of phylogenetic lineages. Mycorrhiza. 2010;20(4):217-63.
33. O’Hanlon R, Harrington TJ. The macrofungal diversity and community of Atlantic oak (Quercus petraea and Q. Robur) forests in Ireland. An. Jard. Bot. Madr. 2012;69(1):107-17. Available from: https://www.redalyc.org/pdf/556/55624809006.pdf
34. Abrego N, Bässler C, Christensen M, Heilmann-Clausen J. Implications of reserve size and forest connectivity for the conservation of wood-inhabiting fungi in Europe. Biol Conserv. 2015;191:469-77. https://ui.adsabs.harvard.edu/link_gateway/2015BCons.191..469A/doi:10.1016/j.biocon.2015.07.005
35. Akata I, Uzun Y, Kaya A. Macromycetes determined in Yomra (Trabzon) district. Turk J Botany. 2014;38(5):999-1012. https://doi.org/10.3906/BOT-1309-22
36. Solak MH, Alli H, Işiloğlu M, Güngör H, Kalmiş E. Contributions to the macrofungal diversity of Antalya Province. Turk J Botany. 2014;38(2):386-97. https://doi.org/10.3906/bot-1302-15
37. Kaya A. Contributions to the macrofungal diversity of Atatürk Dam Lake basin. Turk J Botany. 2015;39(1):162-72. https://doi.org/10.3906/bot-1404-70
38. Shiryaev AG, Zmitrovich IV, Ezhov ON. Taxonomic and Ecological Structure of Basidial Macromycetes Biota in Polar Deserts of the Northern Hemisphere. Contemp. Probl. Ecol. 2018;11(5):458-71. https://doi.org/10.1134/S1995425518050086
39. Uzun Y, Kaya A. New additions to Turkish Pezizales from the Eastern black sea region. Turk J Botany. 2019;43(2):262-70. https://doi.org/10.3906/bot-1802-34
40. Uzun Y, Kaya A. First records of Hydnobolites and Pachyphlodes species from Turkey. Mycotaxon. 2018;133(3):415-21. https://doi.org/10.5248/133.415
41. Shakhova N, Volobuev S. Cultural and enzymatic activity studies of a pathogenic wood-decaying fungus Fomitiporia hippophaeicola (Hymenochaetales, Basidiomycota), recollected in the Eastern Caucasus. Arch Microbiol. 2023;205(249). https://doi.org/10.1007/s00203-023-03587-9?urlappend=%3Futm_source%3Dresearchgate.net%26utm_medium%3Darticle
42. Smith AH, Theirs HD. A contribution toward a monograph of North American species of Suillus. Ann Arbor (MI): privately published; 1964 [cited 2024 Nov]. Available from: https://research.fs.usda.gov/treesearch/49006
43. Wagg C, Bender SF, Widmer F, van der Heijden MGA. Soil biodiversity and soil community composition determine ecosystem multifunctionality. Proc Natl Acad Sci U S A. 2014;111(14):5266-70. https://doi.org/10.1073/pnas.1320054111
44. Piepenbring M. Introducción a la micología en los trópicos. St. Paul (MN): The American Phytopathological Society; 2015. Available from: https://doi.org/10.1094/9780890546147.fm
45. Dorjey K, Kumar S, Sharma YP. The adaptations of high-altitude mushrooms in the cold desert of Ladakh. In: Advances in Asian Human-Environmental Research. Cham: Springer Nature Switzerland; 2023. p. 95–110.
46. Peng Z, Wei S, Hu Y, Qi B, Yuan C, Wang Q, et al. Assessment of Fungal Diversity in Minqin County, a Typical Arid Region in Northwestern China. Curr Microbiol. 2023;80(62). https://doi.org/10.1007/s00284-022-03167-y
47. Vašutová M, Vítovcová K, Manukjanová A, Prach K. Fungal troublemakers – using indicator species with ephemeral fruitbodies to evaluate recovery of formerly extracted raised bogs. Ecol Indic. 2023;154(110574):110574. https://doi.org/10.1016/j.ecolind.2023.110574
48. Stierle AA, Stierle DB. Bioactive Secondary Metabolites Produced by the Fungal Endophytes of Conifers. Natural product communications [Internet]. 2015;10(10):1671-82. Available from: https://pubmed.ncbi.nlm.nih.gov/26669101/
49. Vasco-Palacios AM, Franco-Molano AE, López-Quintero CA, Boekhout T. Biota Colombiana [Internet]. Biota. 2005;6(1). [cited 2024 Nov 24]. Available from: https://revistas.humboldt.org.co/index.php/biota/article/view/153
50. López-Quintero CA, Straatsma G, Franco-Molano AE, Boekhout T. Macrofungal diversity in Colombian Amazon forests varies with regions and regimes of disturbance. Biodivers. Conserv. 2012;21(9):2221–43.
51. Vasco-Palacios AM, Molano AEF. Diversity of Colombian macrofungi (Ascomycota - Basidiomycota) [Internet]. Medellín (Colombia): Universidad de Antioquia; 2019. Available from: https://ipt.biodiversidad.co/sib/resource?r=udea_mhongos_literatura_001
52. da Marcela Vasco-Palacios A, López-Quintero C, Franco-Molano AE, Boekhout T. Austroboletus amazonicus sp. nov. and Fistulinella campinaranae var. scrobiculata, two commonly occurring boletes from a forest dominated by Pseudomonotes tropenbosii (Dipterocarpaceae) in Colombian Amazonia. Mycologia. 2014;106(5):1004-14. https://doi.org/10.3852/13-324
53. Vargas N, Gonçalves SC, Franco-Molano AE, Restrepo S, Pringle A. In Colombia the Eurasian fungus is expanding its range into native, tropical forests. Mycologia. 2019;111(5):758-71. https://doi.org/10.1080/00275514.2019.1636608
54. Royal Botanic Gardens, Kew. Catalogue of Fungi of Colombia [Internet]. 2022 [cited 2024 Nov 24]. Available from: http://kew.iro.bl.uk/downloads/3ff2c9cb-c057-48a8-8b4f-ab516279dcbf
55. Charria-Girón E, Vasco-Palacios AM, Moncada B, Marin-Felix Y. Colombian fungal diversity: Untapped potential for diverse applications. Microbiol Res (Pavia). 2023;14(4):2000–21. https://doi.org/10.3390/microbiolres14040135
56. Aqueveque P, Anke T, Anke H, Sterner O, Becerra J, Silva M. Favolon B, a new triterpenoid isolated from the Chilean Mycena sp. strain 96180. J Antibiot (Tokyo). 2005;58(1):61-4. https://doi.org/10.1038/ja.2005.7
57. Castañeda-Ramírez G, Aguilar-Marcelino L, López-Guillen G. Macroscopic and microscopic fungi with insecticidal activity. Chil J Agric Res. 2022;82(2):348-57. http://dx.doi.org/10.4067/S0718-58392022000200348
58. Rakshith D, Gurudatt DM, Yashavantha Rao HC, Chandra Mohana N, Nuthan BR, Ramesha KP, et al. Bioactivity-guided isolation of antimicrobial metabolite from Xylaria sp [Internet]. Process Biochem. 2020; Available from: https://linkinghub.elsevier.com/retrieve/pii/S1359511319315570
59. Stoyanova K, Gerginova M, Peneva N, Dincheva I, Alexieva Z. Biodegradation and utilization of the pesticides glyphosate and carbofuran by two yeast strains. Processes (Basel). 2023;11(12):3343. https://doi.org/10.3390/pr11123343
Downloads
Download data is not yet available.
