No abstract

Microorganisms are considered a genetic resource with great potential for achieving sustainable development of agricultural areas. The objective of this research was to determine the effect of microorganism application forms on the production of biomass, gas exchange, and nutrient content in upland rice. The experiment was conducted under greenhouse conditions in a completely randomized design in a factorial 7 × 3 + 1, with four replications. The treatments consisted of combining seven microorganisms with three application forms (microbiolized seed; microbiolized seed + soil drenched with a microorganism suspension at 7 and 15 days after sowing (DAS); and microbiolized seed + plant sprayed with a microorganism suspension at 7 and 15 DAS) and a control (water). Treatments with Serratia sp. (BRM32114), Bacillus sp. (BRM32110 and BRM32109), and Trichoderma asperellum pool provided, on average, the highest photosynthetic rate values and dry matter biomass of rice shoots. Plants treated with Burkolderia sp. (BRM32113), Serratia sp. (BRM32114), and Pseudomonas sp. (BRM32111 and BRM32112) led to the greatest nutrient uptake by rice shoots. Serratia sp. (BRM 32114) was the most effective for promoting an increase in the photosynthetic rate, and for the greatest accumulation of nutrients and dry matter at 84 DAS, in rice shoots, which differed from the control treatment. The use of microorganisms can bring numerous benefits of rice, such as improving physiological characteristics, nutrient uptake, biomass production, and grain yield.

The goal of the present study was to characterize anatomical and biochemical changes in rice plant roots in response to seed treatment with rhizobacteria (Burkholderia pyrrocinia (R-46) + Pseudomonas fluorescens (R-55)) and Trichoderma asperellum (Ta: mixture of strains T-06, T-09, T-12, and T-52). The experimental design was completely randomized, with six treatments (R-46, R-55, R-46 + R-55, Ta+ R-46 + R-55, Ta, and control) and ten replicates. Treatments Ta and R-46 + R-55 increased the root length and diameter as well as the cortex expansion and induced a 2% expansion of the aerenchymal space. Treatments Ta and R-46 increased the vascular cylinder diameter. The number of protoxylem poles and metaxylem vessel elements was increased by R-46 and R-55. The total phenol content increased with treatments Ta, R-46 + R-55, R-46, and R-55, and all the treatments increased the flavonoid content. The lignin content increased with the Ta and R-55 treatments. All the root architecture modifications resulting from the interaction between seedlings and bioagents (rhizobacteria and Trichoderma spp.) observed in the present study favored the root plasticity of rice seedlings.

Crop damage by rice sheath blight, Rhizoctonia solani, can decrease rice yield by up to 45 %. The classical control method of rice sheath blight in the Amazon region is the application of fungicides. Therefore, we tested here the efficiency of a biocontrol agent, Trichoderma asperellum, and fungicides. Two experiments of rice cultivation were carried out with seven treatments: four isolates of T. asperellum, a mixture of the four isolates, the fungicide pencycuron, and the control. The first experiment involved a randomized block design, and seed and foliar spray on all plots. The second experiment involved a split-plot design with foliar spray in main plots and the 1-2 foliar sprays in subplots. Results show that all treatments reduced sheath blight progression rate. In the randomized block experiment T. asperellum reduced disease severity by 19 %, increased grain weight by 34 %, and increased yield by 41 %. In the split-plot design experiment, the mixture of the four T. asperellum isolates grain reduced disease severity by 26 %, increased grain weight by 18.5 %, and increased yield by 26 %. Our results show for the first time that a mixed isolates of T. asperellum was efficient in reducing disease severity and increasing yield and grain weight.

This study investigated the effect of silicon (Si) on the resistance of rice plants of the cv. ‘Primavera’ cultivar that were grown in a nutrient solution with 0 (−Si) or 2 mm (+Si) Si to leaf scald, which is caused by Monographella albescens. The leaf Si concentration increased in the +Si plants (4.8 decag/kg) compared to the −Si plants (0.9 decag/kg), contributing to a reduced expansion of the leaf scald lesions. The extent of the cellular damage that was caused by the oxidative burst in response to the infection by M. albescens was reduced in the +Si plants, as evidenced by the reduced concentration of malondialdehyde. Higher concentrations of total soluble phenolics and lignin‐thioglycolic acid derivatives and greater activities of peroxidases (POX), polyphenoloxidases (PPO), phenylalanine ammonia‐lyases (PAL) and lipoxygenases (LOX) in the leaves of the +Si plants also contributed to the increased rice resistance to leaf scald. In contrast, the activities of chitinases and β‐1,3‐glucanases were higher in the leaves of the −Si plants probably due to the unlimited M. albescens growth in the leaf tissues, as indicated by the larger lesions. The results of this study highlight the potential of Si in decreasing the expansion of the leaf scald lesions concomitantly with the potentiation of phenolic and lignin production, and the greater activities of POX, PPO, PAL and LOX rather than simply acting only as a physical barrier to avoid M. albescens penetration.

No abstract

This is the first report on the effect of light intensity and plant growth‐promoting rhizobacteria (PGPR) on the growth of a tropical forage grass, being a relevant study to improve pasture management in conventional farming and integrated crop‐livestock‐forestry systems. In this study, our aim was to evaluate the effects of light intensity and Burkholderia pyrrocinia and Pseudomonas fluorescens inoculation on Brachiaria brizantha cv. BRS Piatã growth, and phenotypic plasticity to shade. The experiment was conducted in a semi‐controlled environment. Seedlings of B. brizantha were allocated to full sun and shade. P. fluorescens and B. pyrrocinia were inoculated individually or co‐inoculated by soil drench, 14 days after seedling emergence. We evaluated morphogenesis, structural and growth parameters. Irrespective of the light regime, co‐inoculated plants had greater leaf area and SPAD index (chlorophyll content). Increase in total biomass production in co‐inoculated plants was over 100% and 300%, under full sun and shade respectively. Co‐inoculated P. fluorescens and B. pyrrocinia increased shade tolerance in B. brizantha, improving plant performance. Co‐inoculation promoted growth in B. brizantha under both sun and shade, indicating its potential as a bio‐fertilizer in conventional and integrated systems, especially in silvopastoral systems, where light availability to pasture growth may be limited.

A resistência a doenças pode ser induzida em plantas tanto por agentes abióticos como por agentes bióticos, por exemplo isolados avirulentos de patógenos. No presente trabalho objetivou-se determinar a concentração de um isolado avirulento (indutor) e o período necessário para induzir resistência em folhas de arroz a um isolado virulento de M. oryzae. Em casa de vegetação, plantas com 18 dias das cultivares Metica-1 e Cica-8 foram pulverizadas com um isolado indutor de resistência, nas concentrações de 0, 10(5), 3x10(5) e 6x10(5) conídios.mL-1 em períodos que antecederam a inoculação do isolado virulento de 24, 48 e 72 horas. A indução da resistência manifestou-se na redução da área foliar afetada e no tipo de lesão. O grau de indução de resistência foi maior na cultivar Metica-1 do que na cultivar Cica-8, em relação a suas respectivas testemunhas. A indução da resistência em Cica-8 foi superior quando o indutor foi aplicado 48 horas antes da aplicação do isolado virulento nas concentrações de 6x10(5) e 3x10(5) conídios.mL-1. Por outro lado, a indução de resistência em Metica-1 foi significativamente maior em todas as concentrações e períodos de aplicações do indutor quando comparados com a testemunha, mas não houve diferença entre os tratamentos de indução.