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1.
Exp Appl Acarol ; 89(3-4): 417-432, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-37071227

RESUMEN

Prosopis laevigata (mesquite; Fabaceae) forms fertility islands in soils of semi-arid lands where microbial diversity concentrates in response to the accumulation of resources in the soil beneath individual plants, promoting organic matter decomposition and nutrient cycling. This phenomenon provides suitable conditions for the proliferation of key edaphic elements such as fungi and mites. Mite-fungal interactions are central for our understanding of nutrient cycling processes in resource-limited arid food webs; yet, no information is available about fertility islands in semi-arid lands. Thus, we aimed to determine in vitro fungal-based feeding preferences and molecular gut content of the oribatid mite species Zygoribatula cf. floridana and Scheloribates cf. laevigatus, which are abundant under the canopy of P. laevigata in an intertropical semi-arid zone in Central Mexico. Our results on the gut content analysis of these oribatid species resulted in the ITS-based identification of the following fungi: Aspergillus homomorphus, Beauveria bassiana, Filobasidium sp., Mortierella sp., Roussoella sp., Saccharomyces cerevisiae, Sclerotiniaceae sp. and Triparticalcar sp. Furthermore, under laboratory conditions both oribatid mite species exhibited feeding preferences on melanized fungi, such as Cladosporium spp., whereas A. homomorphus and Fusarium penzigi were avoided. Our findings indicated that the analyzed oribatid mite species have similar feeding preferences for melanized fungi, which might suggest resource partitioning and a degree of preference, explaining the coexistence of both oribatid species.


Asunto(s)
Fabaceae , Ácaros , Prosopis , Animales , Cadena Alimentaria , Fertilidad , Suelo
2.
Sci Rep ; 12(1): 18280, 2022 10 31.
Artículo en Inglés | MEDLINE | ID: mdl-36316374

RESUMEN

Honey collection evolved from simple honey hunting to the parallel and independent domestication of different species of bees in various parts of the world. In this study, we investigate the extent to which the composition of Apis and stingless bee honeys has been a driver in the selection of different bee species for domestication in Mesoamerica (Mexico) and Asia (Thailand) using a sampling design that combines peak honey profiling by H1 NMR spectroscopy with the collection of honeys from domesticated and undomesticated bee species. Our results show that, independently of the region of the world considered, domesticated stingless bees produce honey whose compositional profiles differ from those of the non-domesticated species and exhibit more similarities towards honeys produced by the domesticated Apis species. Our results provide evidence for the first time that the search for natural sweeteners in the environment by our ancestors led to the parallel and independent domestication of social bees producing honeys with similar compositional profiles.


Asunto(s)
Miel , Abejas , Animales , Miel/análisis , Domesticación , Espectroscopía de Resonancia Magnética , Tailandia , México
3.
J Environ Manage ; 95 Suppl: S25-30, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21295905

RESUMEN

We investigated the diversity of a denitrifying gene (nirK) and the emission of CO(2) and N(2)O, in a "chinampa" soil contaminated with methyl parathion. Soil at 40% of water holding capacity was spiked with methyl parathion at four concentrations (i.e. 0, 0.7, 1.47 and 4.27 g kg(-1) dry soil), while emission of N(2)O and CO(2) and nirK diversity was determined after 0, 1, 14, 30, 60 and 90 days. The emission of N(2)O on a daily base and the cumulative emission of CO(2) was not affected by the different concentrations of methyl parathion applied to soil. The diversity of the nirK gene, determined by using temperature gradient gel electrophoresis (TGGE), decreased with increased methyl parathion application. It was found that methyl parathion had effect on the emissions of N(2)O and CO(2), and reduced the diversity of the nirK gene. Consequently, the reduced diversity of the nirK gene could affect the emission of N(2)O.


Asunto(s)
Insecticidas/metabolismo , Metil Paratión/metabolismo , Óxido Nitroso/metabolismo , Microbiología del Suelo , Contaminantes del Suelo/metabolismo , Dióxido de Carbono/metabolismo , Desnitrificación , Electroforesis/métodos , Genes Bacterianos , México , Datos de Secuencia Molecular , Filogenia
4.
Bioresour Technol ; 102(7): 4618-27, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21310607

RESUMEN

The structure of the biofouling layers formed on a pilot-scale membrane-coupled upflow anaerobic sludge blanket bioreactor (UASB) used to treat urban wastewater was analyzed by scanning electron microscopy and electron-dispersive X-ray microanalysis. For comparison, control samples of the membranes were fed either UASB effluent or raw wastewater in a laboratory-scale experiment. Microbial diversity in the fouling materials was analyzed by temperature gradient gel electrophoresis (TGGE) combined with sequence analysis of partial 16S rRNA. Significant differences in structure of the Bacteria communities were observed amongst the different fouling layers analyzed in the UASB membranes, particularly following a chemical cleaning step (NaClO), while the Archaea communities retained more similarity in all samples. The main Bacteria populations identified were evolutively close to Firmicutes (42.3%) and Alphaproteobacteria (30.8%), while Archaea were mostly affiliated to the Methanosarcinales and Methanospirillaceae. Sphingomonadaceae-related bacteria and methanogenic Archaea were persistently found as components of biofouling, regardless of chemical cleaning.


Asunto(s)
Archaea/genética , Bacterias/genética , Reactores Biológicos/microbiología , Membranas Artificiales , Eliminación de Residuos Líquidos/métodos , Purificación del Agua/métodos , Anaerobiosis , Análisis de Varianza , Bacterias/ultraestructura , Secuencia de Bases , Análisis por Conglomerados , Dermatoglifia del ADN , Cartilla de ADN/genética , Electroforesis en Gel de Gradiente Desnaturalizante , Microanálisis por Sonda Electrónica , Microscopía Electrónica de Rastreo , Datos de Secuencia Molecular , Filogenia , ARN Ribosómico 16S/genética , Análisis de Secuencia de ADN
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