Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America

Los hongos micorrízicos juegan un papel clave en el funcionamiento de los ecosistemas terrestres. Los principales tipos de asociaciones de micorrizas son micorrizas arbusculares (AM), ectomicorrizas (EcM), micorrizas ericoides (ErM) y micorrizas de orquídeas (OM). Estudios anteriores han demostrado...

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Fecha de publicación:: 2020

Institución:: Universidad del Rosario

Repositorio:: Repositorio EdocUR - U. Rosario

Idioma:: eng

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repository_id_str
dc.title.spa.fl_str_mv	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
dc.title.TranslatedTitle.spa.fl_str_mv	Diversidad de tipos de micorrizas a lo largo de gradientes altitudinales en bosques tropicales de montaña del norte de Sudamérica
title	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
spellingShingle	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America Biogeografía Micorrizas Andes colombianos Gradiente altitudinal Diversidad Biología Ciencias botánicas Biogeography Mycorrhizae Colombian Andes Altitudinal gradient Diversity
title_short	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
title_full	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
title_fullStr	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
title_full_unstemmed	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
title_sort	Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America
dc.contributor.advisor.none.fl_str_mv	Bottin, Marius Corrales Osorio, Adriana
dc.subject.spa.fl_str_mv	Biogeografía Micorrizas Andes colombianos Gradiente altitudinal Diversidad
topic	Biogeografía Micorrizas Andes colombianos Gradiente altitudinal Diversidad Biología Ciencias botánicas Biogeography Mycorrhizae Colombian Andes Altitudinal gradient Diversity
dc.subject.ddc.spa.fl_str_mv	Biología Ciencias botánicas
dc.subject.keyword.spa.fl_str_mv	Biogeography Mycorrhizae Colombian Andes Altitudinal gradient Diversity
description	Los hongos micorrízicos juegan un papel clave en el funcionamiento de los ecosistemas terrestres. Los principales tipos de asociaciones de micorrizas son micorrizas arbusculares (AM), ectomicorrizas (EcM), micorrizas ericoides (ErM) y micorrizas de orquídeas (OM). Estudios anteriores han demostrado que la abundancia de plantas AM, ECM y ErM cambia gradualmente a lo largo de gradientes latitudinales y altitudinales impulsados por los efectos del clima en la descomposición, reflejados en la acumulación de carbono y nutrientes en el suelo. La cordillera de los Andes colombianos alcanza altitudes superiores a los 5.000 my es un gran sistema para probar los efectos de la altitud en los ecosistemas tropicales. Nuestro objetivo fue comprender cómo la altitud y las condiciones climáticas y del suelo dan forma a los patrones de distribución de los tipos de micorrizas en las especies de plantas distribuidas en esta región. Para probar esto, usamos una base de datos de registros de plantas de herbario y asignamos el tipo de micorrizas según la literatura disponible. También utilizamos variables bioclimáticas y edáficas a una resolución de 10 km. Calculamos la proporción de cada uno de los diferentes tipos de asociaciones de micorrizas por celda de cuadrícula y creamos un índice de diversidad para explorar su distribución espacial y su asociación con factores abióticos basados en GLM. Encontramos que la diversidad de asociaciones de micorrizas aumenta con la altitud y la reserva de carbono del suelo.
publishDate	2020
dc.date.accessioned.none.fl_str_mv	2020-08-20T20:15:52Z
dc.date.available.none.fl_str_mv	2020-08-20T20:15:52Z
dc.date.created.none.fl_str_mv	2020-07-17
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	Artículo
dc.type.spa.spa.fl_str_mv	Trabajo de grado
dc.identifier.doi.none.fl_str_mv	https://doi.org/10.48713/10336_28203
dc.identifier.uri.none.fl_str_mv	https://repository.urosario.edu.co/handle/10336/28203
url	https://doi.org/10.48713/10336_28203 https://repository.urosario.edu.co/handle/10336/28203
dc.language.iso.spa.fl_str_mv	eng
language	eng
dc.rights.spa.fl_str_mv	Atribución-NoComercial-SinDerivadas 2.5 Colombia
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dc.rights.acceso.spa.fl_str_mv	Abierto (Texto Completo)
dc.rights.uri.none.fl_str_mv	http://creativecommons.org/licenses/by-nc-nd/2.5/co/
rights_invalid_str_mv	Atribución-NoComercial-SinDerivadas 2.5 Colombia Abierto (Texto Completo) http://creativecommons.org/licenses/by-nc-nd/2.5/co/ 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	Averill, C., Turner, B. L., and Finzi, A. C. (2014). Mycorrhiza‐mediated competition between plants and decomposers drives soil carbon storage. Nature, 505, 543–545. https ://doi.org/10.1038/nature12901 Barceló, M., van Bodegom, P. M., and Soudzilovskaia, N. A. (2019). Climate drives the spatial distribution of mycorrhizal host plants in terrestrial ecosystems. Journal of Ecology, 107(6), 2564-2573 Barón, J. D. (2010). Geografía económica de los Andes Occidentales de Colombia (No. 006841). Banco de la República-Economía Regional. Bennett, J. A., Maherali, H., Reinhart, K. O., Lekberg, Y., Hart, M. M., and Klironomos, J. (2017). Plant-soil feedbacks and mycorrhizal type influence temperate forest population dynamics. Science, 355(6321), 181-184 Bonilla, H. (2001). Minería, mano de obra, y circulación monetaria en los Andes colombianos del siglo XVII. Fronteras de la Historia, (6), 142-158. Bottin, M., Peyre, G., Vargas, C., Raz, L., Richardson, J. E., and Sanchez, A. Phytosociological data and herbarium collections show congruent large scale patterns but differ in their local descriptions of community composition. Journal of Vegetation Science. Brundrett, M. C., and Tedersoo, L. (2018). Evolutionary history of mycorrhizal symbioses and global host plant diversity. New Phytologist, 220(4), 1108-1115. Cheeke, T. E., Phillips, R. P., Brzostek, E. R., Rosling, A., Bever, J. D., and Fransson, P. (2017). Dominant mycorrhizal association of trees alters carbon and nutrient cycling by selecting for microbial groups with distinct enzyme function. New Phytologist, 214(1), 432-442 Corrales, A., Mangan, S. A., Turner, B. L., and Dalling, J. W. (2016). An ectomycorrhizal nitrogen economy facilitates monodominance in a neotropical forest. Ecology Letters, 19(4), 383-392 Duque, A., Álvarez, E., Rodríguez, W., and Lema, Á. (2013). Impacto de la fragmentación en la diversidad de plantas vasculares en bosques andinos del nororiente de Colombia. Colombia Forestal, 16(2), 115-137 GALINDO, R., BETANCUR, J., and CADENA, J. J. (2003). Estructura y composición florística de cuatro bosques andinos del santuario de flora y fauna Guanentá-alto río Fonce, cordillera oriental colombiana. Caldasia, 25(2), 313-335. Klironomos, J., Zobel, M., Tibbett, M., Stock, W. D., Rillig, M. C.,. Parrent, J. L., … Bever, J. D. (2011). Forces that structure plant communities: Quantifying the importance of the mycorrhizal symbiosis. New Phytologist, 189, 366–370. https ://doi. org/10.1111/j.1469-8137.2010.03550.x Klironomos, J., Zobel, M., Tibbett, M., Stock, W. D., Rillig, M. C.,. Parrent, J. L., … Bever, J. D. (2011). Forces that structure plant communities: Quantifying the importance of the mycorrhizal symbiosis. New Phytologist, 189, 366–370. https ://doi. org/10.1111/j.1469-8137.2010.03550.x Legendre, P. (2008). Studying beta diversity: ecological variation partitioning by multiple regression and canonical analysis. Journal of Plant Ecology, 1(1), 3-8 Leifheit, E. F., Veresoglou, S. D., Lehmann, A., Morris, E. K., and Rillig, M.C. (2013). Multiple factors influence the role of arbuscular mycorrhizal fungi in soil aggregation—A meta‐analysis. Plant and Soil, 374, 523–537. https ://doi.org/10.1007/s11104-013-1899-2. Mantilla, L. C., Mendoza, H., Bissig, T., and Craig, H. (2011). Nuevas evidencias sobre el magmatismo Miocenico en el distrito minero de Vetas-California (Macizo de Santander, Cordillera Oriental, Colombia). Boletín de Geología, 33(1). Mcguire, K., Henkel, T., De La Cerda, I. G., Villa, G., Edmund, F., and Andrew, C. (2008). Dual mycorrhizal colonization of forest‐dominating tropical trees and the mycorrhizal status of non‐dominant tree and liana species. Mycorrhiza, 18, 217–222. https ://doi.org/10.1007/ s00572-008-0170-9 Read, D. J. (1991). Mycorrhizas in ecosystems. Experientia, 47, 376–391. https ://doi.org/10.1007/BF019 72080 Read, D. J. (1996). The structure and function of the ericoid mycorrhizal root. Annals of Botany, 77(4), 365-374. Read, D. J., Leake, J. R., and Perez‐Moreno, J. (2004). Mycorrhizal fungi as drivers of ecosystem processes in heathland and boreal forest biomes. Canadian Journal of Botany, 82, 1243–1263. https ://doi.org/10.1139/b04-123 Restrepo, J. O. V., Maniguaje, N. L., and Duque, Á. J. (2012). Diversidad y dinámica de un bosque subandino de altitud en la región norte de los Andes colombianos. Revista de Biología Tropical, 60(2), 943-952 Rodríguez, N., Armenteras, D., Morales, M., and Romero, M. (2004). Ecosistemas de los Andes colombianos (No. 333.950986 E19). Siavosh, S., Rivera, J. M., and Gómez, M. E. (2000). Impacto de sistemas de ganadería sobre las características físicas, químicas y biológicas de suelos en los Andes de Colombia. Agroforestería para la Producción Animal en Latinoamérica. FAO-CIPAV, Cali, Colombia, 77-95. Smith, S. E., and Read, D. J. (2008). Mycorrhizal symbiosis. London, UK: Academic Press. Steidinger, B. S., Crowther, T. W., Liang, J., Van Nuland, M. E., Werner, G. D., Reich, P. B., ... and Herault, B. (2019). Climatic controls of decomposition drive the global biogeography of forest-tree symbioses. Nature, 569(7756), 404. Tedersoo, L., and Brundrett, M. C. (2017). Evolution of ectomycorrhizal symbiosis in plants. In Biogeography of mycorrhizal symbiosis (pp. 407-467). Springer, Cham. van de Weg, M. J., Meir, P., Grace, J., and Atkin, O. K. (2009). Altitudinal variation in leaf mass per unit area, leaf tissue density and foliar nitrogen and phosphorus content along an Amazon-Andes gradient in Peru. Plant Ecology and Diversity, 2(3), 243-254 Van Der Heijden, M. G., Klironomos, J. N., Ursic, M., Moutoglis, P., Streitwolf‐Engel, R., Boller, T., … Sanders, I. R. (1998). Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity. Nature, 396, 69. https ://doi.org/10.1038/23932. Veblen, T. T., Young, K. R., and Orme, A. R. (Eds.). (2015). The physical geography of South America. Oxford University Press. Veresoglou, S. D., Chen, B., and Rillig, M. C. (2012). Arbuscular mycorrhiza and soil nitrogen cycling. Soil Biology and Biochemistry, 46, 53–62. https ://doi.org/10.1016/j.soilb io.2011.11.018. Vetrovsky, T., Morais, D., Kohout, P., Lepinay, C., Gallardo, C. A., Holla, S. A., ... and Human, Z. R. (2020). GlobalFungi: Global database of fungal records from high-throughput-sequencing metabarcoding studies. bioRxiv. Wang, B., and Qiu, Y.-L. (2006). Phylogenetic distribution and evolution of mycorrhizas in land plants. Mycorrhiza, 16(5), 299–363. doi:10.1007/s00572-005-0033-6; Harley, J. L., and Harley, E. L. (1987). A check-list of mycorrhiza in the British flora. Xu, H., Detto, M., Fang, S., Chazdon, R. L., Li, Y., Hau, B. C., ... and Uriarte, M. (2020). Soil nitrogen concentration mediates the relationship between leguminous trees and neighbor diversity in tropical forests. Communications biology, 3(1), 1-8. Phillips, R. P., Brzostek, E., and Midgley, M. G. (2013). The mycorrhizal‐associated nutrient economy: a new framework for predicting carbon–nutrient couplings in temperate forests. New Phytologist, 199(1), 41-51. Unger, M., Homeier, J., and Leuschner, C. (2012). Effects of soil chemistry on tropical forest biomass and productivity at different elevations in the equatorial Andes. Oecologia, 170(1), 263-274. Xu, H., Detto, M., Li, Y., Li, Y., He, F., and Fang, S. (2019). Do N‐fixing legumes promote neighbouring diversity in the tropics? Journal of Ecology, 107(1), 229-239. Grizonnet, M., Michel, J., Poughon, V., Inglada, J., Savinaud, M., and Cresson, R. (2017). Orfeo ToolBox: open source processing of remote sensing images. Open Geospatial Data, Software and Standards, 2(1), 1-8. Rangel, J. O. (2005). La biodiversidad de Colombia. Palimpsestvs, (5) de Oliveira, R. A., Ramos, M. M., and de Aquino, L. A. (2015). Irrigation management. In Sugarcane (pp. 161-183). Academic Press. Soudzilovskaia, N. A., Vaessen, S., Barcelo, M., He, J., Rahimlou, S., Abarenkov, K., ... and Tedersoo, L. (2020). FungalRoot: global online database of plant mycorrhizal associations. New Phytologist Nasto, M. K., Alvarez‐Clare, S., Lekberg, Y., Sullivan, B. W., Townsend, A. R., and Cleveland, C. C. (2014). Interactions among nitrogen fixation and soil phosphorus acquisition strategies in lowland tropical rain forests. Ecology Letters, 17(10), 1282-1289 Smith, S. E., and Smith, F. A. (2011). Roles of arbuscular mycorrhizas in plant nutrition and growth: new paradigms from cellular to ecosystem scales. Annual review of plant biology, 62, 227-250 Gavito, M. E., and Azcón–Aguilar, C. (2012). 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The modelled growth of mycorrhizal and non-mycorrhizal plants under constant versus variable soil nutrient concentration. Mycorrhiza, 12(5), 257-261 Craine, J. M., Elmore, A. J., Aidar, M. P., Bustamante, M., Dawson, T. E., Hobbie, E. A., and Nardoto, G. B. (2009). Global patterns of foliar nitrogen isotopes and their relationships with climate, mycorrhizal fungi, foliar nutrient concentrations, and nitrogen availability. New Phytologist, 183(4), 980-992 Zhou, J., Deng, Y., Shen, L., Wen, C., Yan, Q., Ning, D., ... and Voordeckers, J. W. (2016). Temperature mediates continental-scale diversity of microbes in forest soils. Nature communications, 7(1), 1-10 Barron, A. R., Purves, D. W., and Hedin, L. O. (2011). Facultative nitrogen fixation by canopy legumes in a lowland tropical forest. Oecologia, 165(2), 511-520 Menge, D. N., Levin, S. A., and Hedin, L. O. (2009). Facultative versus obligate nitrogen fixation strategies and their ecosystem consequences. The American Naturalist, 174(4), 465-477 Xu, H., Detto, M., Li, Y., Li, Y., He, F., and Fang, S. (2019). Do N‐fixing legumes promote neighbouring diversity in the tropics?. Journal of Ecology, 107(1), 229-239. Xu, H., Detto, M., Fang, S., Chazdon, R. L., Li, Y., Hau, B. C., ... and Uriarte, M. (2020). Soil nitrogen concentration mediates the relationship between leguminous trees and neighbor diversity in tropical forests. Communications biology, 3(1), 1-8 Ayram, C. A. C., Rothlisberger, A. E., Timote, J. J. D., Buritica, S. R., Ramirez, W., and Corzo, G. (2020). Spatiotemporal Evaluation of The Human Footprint in Colombia: Four Decades of Anthropic Impact in Highly Biodiverse Ecosystems. bioRxiv Delavaux, C. S., Weigelt, P., Dawson, W., Duchicela, J., Essl, F., van Kleunen, M., ... and Winter, M. (2019). Mycorrhizal fungi influence global plant biogeography. Nature ecology and evolution, 3(3), 424-429 Lehto, T., and Zwiazek, J. J. (2011). Ectomycorrhizas and water relations of trees: a review. Mycorrhiza, 21(2), 71-90 Van Der Heijden, M. G., Klironomos, J. N., Ursic, M., Moutoglis, P., Streitwolf-Engel, R., Boller, T., ... & Sanders, I. R. (1998). Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity. Nature, 396(6706), 69-72.
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spelling	Bottin, Marius 665908600Corrales Osorio, Adriana43260206600Rendón Espinosa, Miguel ÁngelBiólogoFull time26fa64f0-b066-4abe-8c17-4a41d1901bad6002020-08-20T20:15:52Z2020-08-20T20:15:52Z2020-07-17Los hongos micorrízicos juegan un papel clave en el funcionamiento de los ecosistemas terrestres. Los principales tipos de asociaciones de micorrizas son micorrizas arbusculares (AM), ectomicorrizas (EcM), micorrizas ericoides (ErM) y micorrizas de orquídeas (OM). Estudios anteriores han demostrado que la abundancia de plantas AM, ECM y ErM cambia gradualmente a lo largo de gradientes latitudinales y altitudinales impulsados por los efectos del clima en la descomposición, reflejados en la acumulación de carbono y nutrientes en el suelo. La cordillera de los Andes colombianos alcanza altitudes superiores a los 5.000 my es un gran sistema para probar los efectos de la altitud en los ecosistemas tropicales. Nuestro objetivo fue comprender cómo la altitud y las condiciones climáticas y del suelo dan forma a los patrones de distribución de los tipos de micorrizas en las especies de plantas distribuidas en esta región. Para probar esto, usamos una base de datos de registros de plantas de herbario y asignamos el tipo de micorrizas según la literatura disponible. También utilizamos variables bioclimáticas y edáficas a una resolución de 10 km. Calculamos la proporción de cada uno de los diferentes tipos de asociaciones de micorrizas por celda de cuadrícula y creamos un índice de diversidad para explorar su distribución espacial y su asociación con factores abióticos basados en GLM. Encontramos que la diversidad de asociaciones de micorrizas aumenta con la altitud y la reserva de carbono del suelo.Mycorrhizal fungi play key roles in the functioning of terrestrial ecosystems. The main types of mycorrhizal associations are arbuscular mycorrhizas (AM), ectomycorrhizas (EcM), ericoid mycorrhizas (ErM) and orchid mycorrhizas (OM). Previous studies have shown that the abundance of AM, EcM and ErM plants change gradually along latitudinal and altitudinal gradients driven by the effects of climate on decomposition, reflected in the accumulation of carbon and nutrients in the soil. The Colombian Andean mountain range reaches altitudes over 5,000 m and it is a great system to test the effects of altitude in tropical ecosystems. We aimed to understand how altitude and climatic and soil conditions shape the distribution patterns of mycorrhizal types in plant species distributed in this region. To test this, we used an herbarium plant record database and assigned mycorrhizal type based on the available literature. We also used bioclimatic and soil variables at a resolution of 10 km. We calculated the proportion of each of the different mycorrhizal associations types per grid cell and created a diversity index to explore their spatial distribution and their association with abiotic factors based on GLMs. We found that the diversity of mycorrhizal associations increases with altitude and soil carbon stock.application/pdfhttps://doi.org/10.48713/10336_28203 https://repository.urosario.edu.co/handle/10336/28203engUniversidad del RosarioFacultad de Ciencias Naturales y MatemáticasBiologíaAtribución-NoComercial-SinDerivadas 2.5 ColombiaAbierto (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://creativecommons.org/licenses/by-nc-nd/2.5/co/http://purl.org/coar/access_right/c_abf2Averill, C., Turner, B. L., and Finzi, A. C. (2014). Mycorrhiza‐mediated competition between plants and decomposers drives soil carbon storage. Nature, 505, 543–545. https ://doi.org/10.1038/nature12901Barceló, M., van Bodegom, P. M., and Soudzilovskaia, N. A. (2019). Climate drives the spatial distribution of mycorrhizal host plants in terrestrial ecosystems. Journal of Ecology, 107(6), 2564-2573Barón, J. D. (2010). Geografía económica de los Andes Occidentales de Colombia (No. 006841). Banco de la República-Economía Regional.Bennett, J. A., Maherali, H., Reinhart, K. O., Lekberg, Y., Hart, M. M., and Klironomos, J. (2017). Plant-soil feedbacks and mycorrhizal type influence temperate forest population dynamics. Science, 355(6321), 181-184Bonilla, H. (2001). Minería, mano de obra, y circulación monetaria en los Andes colombianos del siglo XVII. Fronteras de la Historia, (6), 142-158.Bottin, M., Peyre, G., Vargas, C., Raz, L., Richardson, J. E., and Sanchez, A. Phytosociological data and herbarium collections show congruent large scale patterns but differ in their local descriptions of community composition. Journal of Vegetation Science.Brundrett, M. C., and Tedersoo, L. (2018). Evolutionary history of mycorrhizal symbioses and global host plant diversity. New Phytologist, 220(4), 1108-1115.Cheeke, T. E., Phillips, R. P., Brzostek, E. R., Rosling, A., Bever, J. D., and Fransson, P. (2017). Dominant mycorrhizal association of trees alters carbon and nutrient cycling by selecting for microbial groups with distinct enzyme function. New Phytologist, 214(1), 432-442Corrales, A., Mangan, S. A., Turner, B. L., and Dalling, J. W. (2016). An ectomycorrhizal nitrogen economy facilitates monodominance in a neotropical forest. Ecology Letters, 19(4), 383-392Duque, A., Álvarez, E., Rodríguez, W., and Lema, Á. (2013). Impacto de la fragmentación en la diversidad de plantas vasculares en bosques andinos del nororiente de Colombia. 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Diversity of mycorrhizal types along altitudinal gradients in mountain tropical forests of northern South America

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