Potato cultivation and livestock effects on microorganism functional groups in soils from the neotropical high Andean Páramo

Abstract

Páramo ecosystems are of great importance because they are considered hotspots within the Tropical Andes. They are also very important for their role as producers and regulators of water processes in the Neotropic. However, the human occupation of the Colombian Páramos has generated conflict between environmental benefits and productive land uses, specifically the potato cultivation and livestock. To assess possible changes associated with potato cultivation (Solanum tuberosum L.) and livestock on the microbial communities of Páramo soils, the objective of this research was to evaluate the possible effects of potato cultivation and livestock farming on the soil microorganisms associated with different functional groups (nitrogen fixers, phosphate solubilizers and cellulolytic) in the Páramo of Nevados National Natural Park (Nevados NNP), Colombia. Samples were collected from soils under potato cultivation, livestock, and Páramo conservation areas over two climatic seasons (rainy and dry) in three farms at different elevations (3769, 3590, and 3432 m a.s.l.). The microorganisms were isolated using selective culture media for each functional group and identified using molecular markers; microbial diversity was analyzed using multivariate statistical tools. Changes were dependent on land use, elevation, and climate and were statistically significant in the rainy season on all three farms and one of the farms during the dry season. Similarly, the results indicated that climate has a greater impact on the evaluated microbial communities than land use does; the changes were significantly different between the soil under potato cultivation and in conserved Páramo sites at most of the evaluated locations and between soil subjected to livestock farming and Páramo in certain locations. However, the differences between potato cultivation and livestock farming were smaller. This study showed for the first time that the microbial structure (abundance and composition) of microorganism functional groups was different as a result of potato cultivation and livestock farming on Páramo soils, although these changes were dependent on farm elevation and climate.

Climate Vulnerability Assessment of the Espeletia Complex on Páramo Sky Islands in the Northern Andes

“…Conservation efforts may also buffer the impact of climate change on Páramo ecosystems by enhancing their adaptive capacity. Vast areas of Páramo land now safe from conflict are not being rapidly protected, making them susceptible to deforestation for cattle and agriculture (Avellaneda-Torres et al, 2020), and illegal logging (Vásquez et al, 2015) and mining (Pérez-Escobar et al, 2018). Thus, improving the current network of protected areas would help minimizing ongoing threats (Duchicela et al, 2019), especially in the highly diverse Páramo complexes of the Eastern Cordillera where putatively new species are still being discovered (Diazgranados and Sanchez, 2017;Mavárez, 2019a).…”

Grupos Funcionais do Solo: Papel das Comunidades Microbianas Especializadas na Ciclagem de Nutrientes e Sensores de Distúrbios Ambientais

“…Estudos têm utilizado diferentes abordagens para avaliar a ecologia microbiana funcional do solo que incluem a atividade metabólica (Zak et al, 1994;Sofo;Ricciuti, 2019), abundância de grupos específicos (Avellaneda-torres et al, 2020), análise genômica (Oszust;Frac, 2021;Fadiji et al, 2021), metaproteômica (Jouffret et al, 2021) e microcosmos (Santinoni et al, 2019).…”

Cambios en calidad del suelo asociados a la aplicación de técnicas de agricultura ecológica en plantas café bajo diferentes coberturas

“…For the seeding and counting of phosphate solubilizing fungi and bacteria, we used the modified Sundara and Sinha medium (Sundara & Sinha, 1963). The procedure was carried out by incubating the bacteria at 28 ºC for 40 h and the fungi at 20 ºC for six days; for cellulolytic bacteria and fungi, we used a medium whose only source of carbon was 1% carboxymethyl cellulose, where bacteria were incubated at 28 ºC for 48 h and fungi at 20 ºC for six days (Avellaneda-Torres et al, 2014); and, finally, for the nitrogen-fixing bacteria, we used the N-free Rennie medium (Rennie, 1981) and CFU plate count by maintaining the temperature at 28 ºC for 48 h (Avellaneda-Torres et al, 2020).…”