Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama
En el presente estudio se describen Russula floriformis y R. symphoniae como dos nuevas especies hermanas de la subsección Russula Substriatinae del bosque montano presente en Colombia y Panamá asociadas con árboles Quercus spp. y Oreomunnea spp., respectivamente.Las condiciones ambientales en las d...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2020
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/20860
- Acceso en línea:
- https://doi.org/10.48713/10336_20860
https://repository.urosario.edu.co/handle/10336/20860
- Palabra clave:
- America
Bosque montano tropical
Coevolución
Diversidad
Ectomicorriza
Especies cripticas
Fagaceae
Juglandaceae
Botánica
Cryptic species
Coevolution
Diversity
Ectomycorrhiza
Tropical mountain forest
America
Fagaceae
Juglandaceae
Micología
Genética de hongos
Fisiología de los hongos
Russula-Variación (Biología)
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oai:repository.urosario.edu.co:10336/20860 |
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EDOCUR2 |
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Repositorio EdocUR - U. Rosario |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
dc.title.TranslatedTitle.spa.fl_str_mv |
Dos nuevas especies tropicales de Russula asociadas con Quercus muestran evidencia de diversificación en el Istmo de Panamá |
title |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
spellingShingle |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama America Bosque montano tropical Coevolución Diversidad Ectomicorriza Especies cripticas Fagaceae Juglandaceae Botánica Cryptic species Coevolution Diversity Ectomycorrhiza Tropical mountain forest America Fagaceae Juglandaceae Micología Genética de hongos Fisiología de los hongos Russula-Variación (Biología) |
title_short |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
title_full |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
title_fullStr |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
title_full_unstemmed |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
title_sort |
Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of Panama |
dc.contributor.advisor.none.fl_str_mv |
Adamčík, Slavomir Corrales Osorio, Adriana |
dc.contributor.none.fl_str_mv |
Adamčíková, Katarína Hampe, Felix Caboň, Miroslav Manz, Cathrin Ovrebo, Clark Pipenbring, Meike |
dc.subject.spa.fl_str_mv |
America Bosque montano tropical Coevolución Diversidad Ectomicorriza Especies cripticas Fagaceae Juglandaceae |
topic |
America Bosque montano tropical Coevolución Diversidad Ectomicorriza Especies cripticas Fagaceae Juglandaceae Botánica Cryptic species Coevolution Diversity Ectomycorrhiza Tropical mountain forest America Fagaceae Juglandaceae Micología Genética de hongos Fisiología de los hongos Russula-Variación (Biología) |
dc.subject.ddc.spa.fl_str_mv |
Botánica |
dc.subject.keyword.spa.fl_str_mv |
Cryptic species Coevolution Diversity Ectomycorrhiza Tropical mountain forest America Fagaceae Juglandaceae |
dc.subject.lemb.spa.fl_str_mv |
Micología Genética de hongos Fisiología de los hongos Russula-Variación (Biología) |
description |
En el presente estudio se describen Russula floriformis y R. symphoniae como dos nuevas especies hermanas de la subsección Russula Substriatinae del bosque montano presente en Colombia y Panamá asociadas con árboles Quercus spp. y Oreomunnea spp., respectivamente.Las condiciones ambientales en las dos áreas de estudio son muy similares y una similitud de secuencia ITS superior al 99% con solo 3 posiciones diferentes indican que estas especies están estrechamente relacionadas y son casi crípticas. Observaciones detalladas de estructuras microscópicas y análisis de multi-locus revelaron más caracteres morfológicos y moleculares que distinguen las colecciones de Colombia y Panamá, resultadon en las especies R. floriformis y R. symphoniae. La distribución espacial y la proximidad filogenética de las especies de Russula y la distribución de Quercus, sugiere su especiación como resultado de la migración, la adaptación y el aislamiento climático a través del Istmo de Panamá de la especie durante los eventos del Plioceno y el Pleistoceno. Basado en esto, hipotetizamos que esto podría ser evidencia de coevolución entre Russula y Quercus. El análisis de los datos de secuencia ITS disponibles públicamente sugiere que hay más especies adaptadas localmente de este linaje en América Central y del Norte. |
publishDate |
2020 |
dc.date.accessioned.none.fl_str_mv |
2020-02-12T19:42:35Z |
dc.date.available.none.fl_str_mv |
2020-02-12T19:42:35Z |
dc.date.created.none.fl_str_mv |
2020-01-24 |
dc.type.eng.fl_str_mv |
bachelorThesis |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_7a1f |
dc.type.document.spa.fl_str_mv |
Trabajo de grado |
dc.type.spa.spa.fl_str_mv |
Trabajo de grado |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.48713/10336_20860 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/20860 |
url |
https://doi.org/10.48713/10336_20860 https://repository.urosario.edu.co/handle/10336/20860 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Universidad del Rosario |
dc.publisher.department.spa.fl_str_mv |
Facultad de Ciencias Naturales y Matemáticas |
dc.publisher.program.spa.fl_str_mv |
Biología |
institution |
Universidad del Rosario |
dc.source.bibliographicCitation.spa.fl_str_mv |
Adamčík S, Jančovičová S, & Buyck B. 2018. The Russulas Described by Charles Horton Peck. Cryptogamie Mycologie, 39: 3–108. Adamčík S, Looney B, Caboň M, Jančovičová S, Adamčíková K, Avis PG. Barajas M, Bhatt RP, Corrales A, Das K, Hampe F, Ghosh A, Gates G, Kälvläinen V, Khalid AN, Kiran M, De Lange R, Lee H, Lim YW, Kong A, Manz C, Ovrebo C, Saba M, Taipale T, Verbeken A, Wisitrassameewong K, Buyck B. 2019. The quest for a globally comprehensible Russula language. Fungal Diversity. Adamčík S, Slovák M, Eberhardt U, Ronikier A, Jairus T, Hampe F, Verbeken A (2016b) Molecular inference, multivariate morphometrics and ecological assessment are applied in concert to delimit species in the Russula clavipes complex. Mycologia 108:716–730. https://doi.org/10.3852/15-194 Andersen KM, Endara MJ, Turner BL, Dalling JW. 2012. Trait-based community assembly of understory palms along a soil nutrient gradient in a lower montane tropical forest. Oecologia 168:519–531 Ávila-de Navia SL, Estupiñan-Torres SM. 2013. Calidad sanitaria del agua del Parque Natural Chicaque. NOVA 11:45-51. Bacon CD, Silvestro D, Jaramillo C, Smith BT, Chakrabarty P, Antonelli, A. 2015. Biological evidence supports and early and complex emergence of the Isthmus of Panama. Proceeding of the National Academy of Sciences 112: 6110-6115. Badotti F, Silva de Oliveira F, Garcia CF, Vaz AMB, Fonseca PLC, Nahum LA, Oliveira G, Góes-Neto A. 2017. Effectiveness of ITS and sub-regions as DNA barcode markers for the identification of Basidiomycota (Fungi). BMC Microbiology 17: 42. Bazzicalupo AL, Buyck B, Saar I, Vauras J, Carmean D, Berbee ML. 2017. Troubles with mycorrhizal mushroom identification where morphological differentiation lags behind barcode sequence divergence. Taxon 66(4):791–810. Becerra G, Zak M. 2011. The Ectomycorrhizal Symbiosis in South America: Morphology, Colonization, and Diversity. In: Baptista P, Tavares RM, Lino-Neto T. 2011. Diversity and Biotechnology of Ectomycorrhizae. Berlin, Germany. p. 157–175. Becerra A, Zak MR, Horton TR, Micolini J. 2005. Ectomycorrhizal and arbuscular mycorrhizal colonization of Alnus acuminata from Calilegua National Park (Argentina). Mycorrhiza. 15: 525–531. Buyck B. 1989. Valeur taxonomique du bleu de crésyl pour le genre Russula. Bull Soc Mycol Fr 105:1–6 Buyck B. 1992. Checklist of tropical Russulae. Russulales News, Special Issue 1: 1-100 Buyck B, Adamčík S. 2011. Type Studies in Russula Subgenus Heterophyllidia from the Eastern United States. Cryptogamie, Mycologie, 32: 151–169. Buyck B, Halling R. 2004. Two new Quercus-associated Russulas from Costa Rica and their relation to some very rare North American species. Cryptogamie, Mycologie, 25: 3–13. Buyck B, Halling RE, Miller GM. 2003. The inventory of Russula in Costa Rica: discovery of two very rare North American species in montane oak forest. Bolletino del Gruppo Micologico G. Bresadola – Nuova Serie 46(3): 57–74 Buyck B, Zoller S, Hofstetter V. 2018. Walking the thin line… ten years later: the dilemma of above- versus below-ground features to support phylogenies in the Russulaceae (Basidiomycota). Fungal Diversity 89: 267–292. Caboň M, Eberhardt U, Looney B, Hampe F, Kolařík M, Jančovičová S, Verbeken A, Adamčík S. 2017. New insights in Russula subsect. Rubrinae: phylogeny and the quest for synapomorphic characters. Mycological Progress, 16: 877–892. Caboň M, Li GJ, Saba M, Kolařík M, Jančovičová S, Khalid AN, Moreau PA, Wen HA, Pfister DH, Adamčík S. 2019. Phylogenetic study documents different speciation mechanisms within the Russula globispora lineage in boreal and arctic environments of the Northern Hemisphere. IMA Fungus 10: 1–16 Cavelier J .1996. Fog interception in montane forests across the central cordillera of Panama. J Trop Ecol 12:357–369 Corrales A, Arnold AE, Ferrer A, Turner BL, Dalling JW. 2016. Variation in ectomycorrhizal fungal communities associated with Oreomunnea mexicana (Juglandaceae) in a Neotropical montane forest. Mycorrhiza 26: 1–17. Corrales A, Henkel TW, Smith ME. 2018. Ectomycorrhizal associations in the tropics – biogeography, diversity patterns and ecosystem roles. New Phytologist, 220: 1076–1091. Correa A, Galdames C, Stapf MS. 2004. Catalogue of vascular plants of Panama. Universidad de Panamá, Instituto de Investigaciones Tropicales Del Olmo-Ruiz M, García-Sandoval R, Alcántara-Ayala O, Véliz M, Luna-Vega I. 2017. Current knowledge of fungi from Neotropical montane cloud forests: distributional patterns and composition. Biodiversity and Conservation 26: 1919–1942. Diédhiou AG, Selosse MA, Galiana A, Diabaté M, Dreyfus B, Bâ AM, de Faria SM, Béna, G. 2010. Multi-host ectomycorrhizal fungi are predominant in a Guinean tropical rainforest and shared between canopy trees and seedlings. Environmental Microbiology 12: 2219–2232. Franco-Molano AE, Corrales A, Vasco-Palacios AM. 2010. Macrogundi of Colombia II. Checklist of the species of Agaricales, Boletales, Cantharellales and Russulales (Agaricomycetes, Basidiomycota). Actualidad Biologicas 32: 89-114. García-Guzmán OM, Garibay-Orijel R, Hernández E, Arellano-Torres E, & Oyama K. 2017. Word-wide meta-analysis of Quercus forests ectomycorrhizal fungal diversity reveals southwestern Mexico as a hotspot. Mycorrhiza 27: 811–822. Gardes M, Bruns TD. 1993. ITS primers with enhanced specificity for basidiomycetes-application to the identification of mycorrhizae and rusts. Molecular Ecology 2:113–118. González CE, Jarvis A, Palacio JD. 2006. Biogeography of the Colombian oak, Quercus humboldtii Bonpl: geographical distribution and their climatic adaptation. International Centre for Tropical Agriculture (CIAT)/Museo de Historia Natural, Universidad Del Cauca.10p. Hall T. 2005. BioEdit: Biological Sequence Alignment Editor. http://www.mbio.ncsu.edu/bioedit/bioedit.html Haug I, Weiß M, Homeier J, Oberwinkler F, Kottke I. 2005. Russulaceae and Thelephoraceae form ectomycorrhizas with members of the Nyctaginaceae (Caryophyllales) in the tropical mountain rain forest of southern Ecuador. New Phytologist, 165: 923–936. Hynes MM, Smith ME, Zasoski RJ, Bledsoe CS. 2010. A molecular survey of ectomycorrhizal hyphae in a California Quercus–Pinus woodland. Mycorrhiza 20: 265–274 Herrera F, Manchester SR, Koll R, Jaramillo C. 2014. Fruits of Oreomunnea (Juglandaceae) in the early Miocene of Panama. In: Stevens WD, Montiel OM, Raven PH, Paleobotany and Biogeography: A Festschrift for Alan Graham in His 80th Year, 124–133. St Louis. Missouri Botanical Garden Press. Hooghiemstra H. 2006. Immigration of Oak into Northern South America: A Paleo-Ecological Document. In: Kappelle M. Ecology and Conservation of Neotropical Montane Oak Forests. Berlin, Germany. Springer. p 17–28. Jaramillo C. 2018. Evolution of the Isthmus of Panama: Biological, Paleoceanographic and Paleoclimatological Implications. In: Hoorn C, Perrigo A, Antonelli A, Mountains, Climate and Biodiversity. Hoboken, New Jersey. John Wiley & Sons. P 323-337. Katoh K., Standley D.M. 2013. MAFFT multiple sequence alignment software, version 7: improvements in performance and usability. Molecular Biology and Evolution 30:772–780 Kearse M., Moir R., Wilson A., Stones-Havas S., Cheung M. et al. 2012. Geneious basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics 28:1647–1649 Lanfear R., Calcott B., Ho S.Y., Guindon S., Lanfear R. et al. 2012. PartitionFinder: combined selection of partitioning schemes and substitution models for phylogenetic analyses. Molecular Biology and Evolution 29:1695–1701 Looney BP, Meidl P, Piatek MJ, Miettinen O, Martin FM, Matheny PB, Labbé JL. 2018. Russulaceae: a new genomic dataset to study ecosystem function and evolutionary diversification of ectomycorrhizal fungi with their tree associates. New Phytologist 218: 54–66. Looney BP, Ryberg M, Hampe F, Sánchez-García M, Matheny PB. 2016. Into and out of the tropics: Global diversification patterns in a hyperdiverse clade of ectomycorrhizal fungi. Molecular Ecology 25: 630–647. Manz C. 2019. Diversity assessment of the ectomycorrhizal genus Russula in tropical montane forests in Masterarbeit. Matheny PB .2005 Improving phylogenetic inference of mushrooms with RPB1 and RPB2 nucleotide sequences (Inocybe; Agaricales). Mol Phylogenet Evol 35:1–20. doi:10.1016/j.ympev.2004.11.014 Miller M.A., Pfeiffer W., Schwartz T. 2010 Creating the CIPRES Science Gateway for inference of large phylogenetic trees. Proceedings of the Gateway Computing Environments Workshop (GCE), 14 Nov. 2010, New Orleans, LA pp 1 - 8. Moncalvo JM, Lutzoni FM, Rehner SA, Johnson J, Vilgalys R (2000) Phylogenetic relationship of agaric fungi based on nuclear large subunit ribosomal DNA sequences. Syst Biol 49(2): 278–305. https://doi.org/10.1093/sysbio/49.2.278 Morehouse EA, James TY, Ganley ARD, Vilgalys R, Berger L, Murphy PJ, Longcore E. 2003 – Multilocus sequences typing suggests the chytrid pathogen of amphibians is a recently emerged clone. Molecular Ecology 12:395–403 Nilsson RH, Ryberg M, Kristiansson E, Abarenkov K, Larsson KH, Köljalg U. 2006. Taxonomic reliability of DNA sequences in public sequences databases: A fungal perspective. PLoS ONE 1: e59 Nixon KC. 2006. Global and Neotropical Distribution and Diversity of Oak (genus Quercus) and Oak Forests. In: Ecology and Conservation of Neotropical Montane Oak Forests. Berlin, Germany. Springer. p. 3–13. Ondrušková E, Jánošíková Z, Kádasi-Horáková M, Koltay A, Ostrovský R, Pažitný J, Adamčíková K. 2017 – Distribution and characterization of Dothistroma needle blight pathogens on Pinus mugo in Slovakia. European Journal of Plant Pathology 148(2):283–294. https://link.springer.com/article/10.1007/s10658-016-1088-2 Pastirčáková K, Adamčíková K, Pastirčák M, Zach P, Galko J, Kováč M, Laco J. 2018 – Two blue-stain fungi colonizing Scots pine (Pinus sylvestris) trees infested by bark beetles in Slovakia, Central Europe. Biologia 73(11):1053–1066. Rambaut A., Suchard M.A., Xie D., Drummond A.J. 2013. Tracer. Version 1.6. http://beast.bio.ed.ac.uk/software/tracer/ Rangel JO, Avella A. 2011. Oak forests of Quercus humboldtii in the Caribbean region and distribution patterns related with environmental factor in Colombia. Plant Biosystems 145: 186-198. Richard F, Millot S, Gardes M, Selosse M-A. 2005. Diversity and specificity of ectomycorrhizal fungi retrieved from an old-growth Mediterranean forest dominated by Quercus ilex. New Phytologist 166: 1011–1023. Rivera-Ospina D, Córdoba-García C. 1998. Guía ecológica Parque Natural Chicaque. Bogotá, Colombia, Jardín Botánico de Bogotá José Celestino Mutis. Rodríguez-Correa F, Oyama K, MacGregor-Fors I, González-Rodríguez A. 2015. How are oaks distributed in the Neotropics? A perspective from species turnover, areas of endemism and climatic niches. International Journal of Plant Sciences 176: 222-231. Romagnesi H (1967) Les Russules D’Europe et D’Afrique du Nord. Bordas, Paris Ronquist F., Teslenko M., van der Mark P., Avres D.L., Darling A. et al. 2012. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice, across a large model space. Systematic Biology 61:539–542 Roy M, Schimann H, Braga-Neto R, Da Silva RAE, Duque J, Frame D, Frame D, Wartchow F, Neves MA. 2016. Diversity and Distribution of Ectomycorrhizal Fungi from Amazonian Lowland White-sand Forests in Brazil and French Guiana. Biotropica 48: 90–100. Roy M, Vasco-Palacios A, Geml J, Buyck B, Delgat L, Giachini A, Grebenc T, Harrower, E, Kuhar F, Magnano A, Rinaldi A, Shimann H, Selosse MA, Sulzbacher MA, Warthchow F, Neves, M. A. 2017. The (re)discovery of ectomycorrhizal symbioses in Neotropical ecosystems sketched in Florianópolis. New Phytologist 214: 920–923. Silvestro D., Michalak I. 2012. raxmlGUI: a graphical front-end for RAxML. Organismal Diversity and Evolution 12:335–337 Smith ME, Henkel TW, Aime CM, Fremier AK, Vilgalys R. 2011. Ectomycorrhizal fungal diversity and community structure on three co-occurring leguminous canopy tree species in a Neotropical rainforest. New Phytologist 192: 699–712. Stamatakis A. 2008. The RAxML 7.0.4 manual. https://web.natur.cuni.cz/~vlada/moltax/RAxML-Manual.7.0.4.pdf Vasco-Palacios AM, Franco-Molano AE. 2013. Diversity of Colombian macrofungi (Ascomycota-Basidiomycota). Mycotaxon. 121:499 Wang J, Buyck B, Wang XH, Bau T. 2019. Visiting Russula (Russulaceae, Russulales) with samples from southwestern China finds one new subsection of R. subg. Heterophyllidia with two new species. Mycological Progress 18: 771–784. Wang Q, He XH, Guo L-D. 2012. Ectomycorrhizal fungus communities of Quercus liaotungensis Koidz of different ages in a northern China temperate forest. Mycorrhiza 22: 461–470 White TJ, Bruns T, Lee S, Taylor J. 1990. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ (eds) PCR Protocols: a guide to methods and applications. Academic Press, San Diego, pp 315–322 Wu Q, Mueller GM, Ovrebo CL. 1997. An index to Genera, Species and Infraspecific Taxa of Basidiomycete Fungi described by Rolf Singer. In: Mueller GM, Wu Q (eds) Mycological contributions of Rolf Singer: Field Itinerary, Index to New Taxa, and List of Publications. Fieldiana, Field Museam of Natural History, Chicago, Illinois, pp 90-93 Ye J, Coulouris G, Zaretskaya I, Cutcutache I, Rozen S, Madden TL. 2012. Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction. BMC Bioinformatics 13:134. Quercus L. in GBIF Secretariat (2019). GBIF Backbone Taxonomy. Checklist dataset https://doi.org/10.15468/39omei accessed via GBIF.org |
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Adamčíková, KatarínaHampe, FelixCaboň, MiroslavManz, CathrinOvrebo, ClarkPipenbring, MeikeAdamčík, Slavomir06de3a4e-e6ff-45d1-bd2f-c8b80333fc32-1Corrales Osorio, Adriana43260206600Vera Castellanos, MichelleBiólogoFull time5692445e-69fa-4c55-b154-111386ec5baa6002020-02-12T19:42:35Z2020-02-12T19:42:35Z2020-01-24En el presente estudio se describen Russula floriformis y R. symphoniae como dos nuevas especies hermanas de la subsección Russula Substriatinae del bosque montano presente en Colombia y Panamá asociadas con árboles Quercus spp. y Oreomunnea spp., respectivamente.Las condiciones ambientales en las dos áreas de estudio son muy similares y una similitud de secuencia ITS superior al 99% con solo 3 posiciones diferentes indican que estas especies están estrechamente relacionadas y son casi crípticas. Observaciones detalladas de estructuras microscópicas y análisis de multi-locus revelaron más caracteres morfológicos y moleculares que distinguen las colecciones de Colombia y Panamá, resultadon en las especies R. floriformis y R. symphoniae. La distribución espacial y la proximidad filogenética de las especies de Russula y la distribución de Quercus, sugiere su especiación como resultado de la migración, la adaptación y el aislamiento climático a través del Istmo de Panamá de la especie durante los eventos del Plioceno y el Pleistoceno. Basado en esto, hipotetizamos que esto podría ser evidencia de coevolución entre Russula y Quercus. El análisis de los datos de secuencia ITS disponibles públicamente sugiere que hay más especies adaptadas localmente de este linaje en América Central y del Norte.Russula floriformis and R. symphoniae are described as two new sister species of Russula subsection Substriatinae from montane forest of Colombia and Panama and associated with Quercus and Oreomunnea trees. Very similar field environmental conditions and an ITS sequence similarity higher than 99% with only 3 different positions indicate that these species are closely related and nearly cryptic. Detailed observations of microscopic structures and analyses of more DNA loci revealed more morphological and molecular characters distinguishing collections of R. floriformis from Colombia and R. symphoniae from Panama. Spatial distribution and phylogenetic proximity of Russula species and their ectomycorrhizal host Quercus tree suggests their speciation as a result of migration, adaptation and climatic isolation across the Panama Isthmus of their host tree during the Pliocene and Pleistocene events. Then we hypothesize that this could be evidence of coevolution between Russula and Quercus. Analysis of publicly available ITS sequence data suggests that there are more locally adapted species of this lineage in Central and North America.2022-02-13 01:01:01: Script de automatizacion de embargos. info:eu-repo/date/embargoEnd/2022-02-12International Association for Plant TaxonomySlovak Academy of Scienceapplication/pdfhttps://doi.org/10.48713/10336_20860 https://repository.urosario.edu.co/handle/10336/20860engUniversidad del RosarioFacultad de Ciencias Naturales y MatemáticasBiologíaAbierto (Texto Completo)EL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma.http://purl.org/coar/access_right/c_abf2Adamčík S, Jančovičová S, & Buyck B. 2018. The Russulas Described by Charles Horton Peck. Cryptogamie Mycologie, 39: 3–108.Adamčík S, Looney B, Caboň M, Jančovičová S, Adamčíková K, Avis PG. 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Checklist dataset https://doi.org/10.15468/39omei accessed via GBIF.orginstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAmericaBosque montano tropicalCoevoluciónDiversidadEctomicorrizaEspecies cripticasFagaceaeJuglandaceaeBotánica581600Cryptic speciesCoevolutionDiversityEctomycorrhizaTropical mountain forestAmericaFagaceaeJuglandaceaeMicologíaGenética de hongosFisiología de los hongosRussula-Variación (Biología)Two new tropical Russula species associated with Quercus show evidence of diversification across the Isthmus of PanamaDos nuevas especies tropicales de Russula asociadas con Quercus muestran evidencia de diversificación en el Istmo de PanamábachelorThesisTrabajo de gradoTrabajo de gradohttp://purl.org/coar/resource_type/c_7a1fORIGINALSupplementary material_1.pdfSupplementary material_1.pdfMaterial Suplementario 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