In vitromorphogenesis of gypsophila: Response to exogenous phytohormones / Morfogênese de gypsophila in vitro: Resposta a fitormônios exógenos

The success of in vitro cultivation of plant species depends on factors associated with the induction and control of morphogenesis regarding the regeneration of shoots and roots in the organogenesis process, such as the culture medium composition. Thus, the objective of this study was to investigate if theconcentration of growth regulators in culture medium interferes with the in vitro morphogenesis of gypsophila. 'Golan' cultivar was subjected to three culture media (M), which constituted the study treatments: M1) Murashige and Skoog (MS) medium without the addition of growth regulators; M2) MS + 1 mg L-1of benzylaminopurine (BAP) + 0.05 mg L-1of naphthaleneacetic acid (NAA); M3) MS + 0.05 mg L-1BAP + 1 mg L-1NAA. After 45 days, the multiplication rate, plant height and root length were evaluated. The results showed that plantlets produced in M2 medium had a higher multiplication rate. Also, plantlets produced in M1 and M3 media showed higher shoot height and root length. It is concluded that there is a difference in the in vitromorphogenesis of gypsophila according to the concentration of growth regulators in the micropropagation medium.(AU)

O sucesso do cultivo in vitro de espécies vegetais depende de fatores associados à indução e ao controle da morfogênese quanto à regeneração de brotos e raízes no processo de organogênese, a exemplo da composição de meio de cultura. Assim, o objetivo do estudo foi investigar se a concentração de reguladores de crescimento em meio de cultura interfere na morfogênese in vitrode gipsofila. A cultivar 'Golan' foi submetida a três meios de cultura (M), que constituíram os tratamentos do estudo: M1) meio Murashige e Skoog (MS) sem adição de reguladores de crescimento; M2) MS + 1 mg.L-1de benzilaminopurina (BAP) + 0.05 mg.L-1de ácido naftalenoacético (ANA); M3) MS + 0.05 mg.L-1BAP + 1 mg.L-1de ANA. Após 45 dias avaliou-se a taxa de multiplicação, altura de plantas e comprimento de raízes. Os resultados mostraram que plântulas produzidas no meio M2 tiveram maior taxa de multiplicação. Ainda, plântulas produzidas nos meios M1 e M3 apresentaram maior altura de parte aérea e comprimento de raízes. Conclui-se que há diferença na morfogênese in vitrode gipsofila de acordo com a concentração de reguladores de crescimento em meio de cultura na micropropagação.(AU)

Screening of the hatching control of root-knot nematodes using extract concentrations from oat genotypes

Even though oats (Avena spp.) have the capacity to produce numerous compounds with the potential to act antagonistically against plant pathogens, studies on the genotypic effect of this crop focusing on their nematicidal activity are limited. The objective of this study was to verify the effect of the aqueous extracts prepared with the biomass of oat genotypes, on the hatching of second-stage juveniles of root-knot nematodes (Meloidogyne javanica and Meloidogyne incognita). The bioassays were carried out in a completely randomized design with four replications. Eighteen extracts were evaluated, consisting of a combination of six oat genotypes Agro Quaraí, Agro Esteio, Embrapa 139, AF 12202, UPFPS Farroupilha, and AF 1345 Ucraniana, and three extract concentrations (5 %, 10 %, and 20 % w/v). Three additional treatments were added to the study (distilled water, chemical nematicides abamectin, and imidacloprid + thiodicarb). The treatments and the suspension containing nematode eggs were placed in Petri dishes and incubated in a growth chamber for ten days. At the 5 % and 10 % w/v concentration levels, a genotype effect was observed in the hatching of juveniles for both nematode species. For the control of M. javanica the extracts of Embrapa 139 had a better performance, while the extracts of Agro Quaraí and AF1345 Ucraniana performed better when under the control of M. incognita. Thus, oat biomass formation might have the ability to suppress the nematode population in the soil, and could therefore, be used for the management of root-knot nematodes.

Micorrhizal biotechnology as an alternative to potentialize the strawberry quality / Biotecnologia micorrízica como alternativa para potencializar a qualidade do morangueiro

The need to develop and use biotechnology tools to improve management and nutritional techniques in strawberry cultivation are increasing. Based on this, the objective of this study was to test if the mycorrhizal inoculation changes the agronomic and qualitative performance of strawberry fruits. The strawberry daughters plants used were of the cultivar Camarosa. The study was carried out in an agricultural greenhouse, Horticulture Sector of the Faculty of Agronomy and Veterinary Medicine (FAMV) of UPF, in the city of Passo Fundo, Rio Grande do Sul (RS), Brazil. The experiment was developed and maintained from June to December 2015. The treatments consisted of five inoculum: T1 = no inoculum (control); T2 = Acaulospora morrowiae; T3 = Rhizophagus clarus; T4 = mycorrhizal community; T5 = Claroideoglomus etunicatum. The experimental design was a randomized block with four replicates. Each plot consisted of a bag containing 6 plants spaced 0.15 mx 0.15 m. In the pits of the plants, it was applied, with the aid of syringe and water, about 70 infective propagules of the tested inocula. During the conduction of the experiment the temperature and photosynthetically active radiation (PAR) were monitored in the culture environment. It was evaluated the agronomic and qualitative performance of the fruits and the percentage of mycorrhizal colonization of the plants roots. The data were submitted to analysis of variance and the differences between means were compared by the Tukey test at 5% of probability error. The cultivar Camarosa produced more fruits in October. In September, the month before the one with the best agronomic performance, the mean temperature was 17.7 ºC. The mean PAR recorded in the growing environment was low in relation to crop requirements, throughout the growing period. Fruits produced by plants inoculated with A. morrowiae presented higher values of TSS/TTA ratio in September and October. The percentage of mycorrhizal colonization varied from 26.2% for A. morrowiae to 46.2% for R. clarus. The inoculation of arbuscular mycorrhizal fungi does not alter the production of strawberry fruits. However, when the plants are inoculated with A. morrowiae there is an improvement in the fruit flavor.

A necessidade de desenvolver e usar ferramentas biotecnológicas para melhorar o manejo e as técnicas nutricionais no cultivo do morangueiro está aumentando. Com base nisso, o objetivo desse estudo foi testar se a inoculação micorrízica altera o desempenho agronômico e qualitativo de frutos de morangueiro. As mudas de morangueiro usadas foram da cultivar Camarosa. O estudo foi realizado em estufa agrícola, no Setor de Horticultura da Faculdade de Agronomia e Medicina Veterinária (FAMV) da UPF, na cidade de Passo Fundo, Rio Grande do Sul (RS), Brasil. O experimento foi desenvolvido e mantido de junho a dezembro de 2015. Os tratamentos consistiram em cinco inóculos: T1 = sem inóculo (controle); T2 = Acaulospora morrowiae; T3 = Rhizophagus clarus; T4 = comunidade micorrízica; T5 = Claroideoglomus etunicatum. O delineamento experimental foi em blocos casualizados, com quatro repetições. Cada parcela consistiu de um saco contendo 6 plantas espaçadas de 0.15 mx 0.15 m. Na cova de plantio das plantas, foi aplicado, com auxílio de seringa e água, cerca de 70 propágulos infectivos dos inóculos testados. Durante a condução do experimento, a temperatura e a radiação fotossinteticamente ativa (PAR) foram monitoradas no ambiente de cultivo. Foi avaliado o desempenho agronômico e qualitativo dos frutos e a porcentagem de colonização micorrízica das raízes das plantas. Os dados foram submetidos à análise de variância e as diferenças entre médias foram comparadas pelo teste de Tukey, a 5% de erro de probabilidade de erro. A cultivar Camarosa produziu mais frutos em outubro. Em setembro, no mês anterior ao de melhor desempenho agronômico, a temperatura média foi de 17.7ºC. A PAR média registrada no ambiente de cultivo foi baixa em relação às necessidades da cultura durante todo o período de cultivo. Frutos produzidos por plantas inoculadas com A. morrowiae apresentaram maiores valores da relação SST/ATT em setembro e outubro. A porcentagem de colonização micorrízica variou de 26.2% para A. morrowiae a 46.2% para R. clarus. A inoculação de fungos micorrízicos arbusculares não altera a produção de frutos de morangueiro. No entanto, quando as plantas são inoculadas com A. morrowiae, há uma melhora no sabor dos frutos.

Biochemical Profile of the Soybean Seed Embryonic Axis and Its Changes during Accelerated Aging.

Seed deterioration is an important topic in plant science, as the majority of cultivated species use seeds as their means of propagation; however, due to its complexity, the process of seed deterioration has not yet been completely elucidated. Three soybean cultivars (BMX Raio, BMX Zeus, and DM 53i54) exposed to four distinct periods of accelerated aging (0, 3, 6 and 9 days) in a fully randomized experimental design. Initially, vigor and germination tests were performed. The activity of superoxide dismutase, catalase, ascorbate peroxidase enzymes, hydrogen peroxide, malonaldehyde, DNA oxidation, macromolecules and mineral content, and Maillard reactions were quantified in the embryonic axis. Results showed that DNA did not suffer degradation or oxidation. In terms of consumption of reserves, only sugars were consumed, while levels of protein, starch, and triglycerides were maintained. The Maillard reaction did show potential as an indicator of buffer capacity of protein to ROS. Additionally, levels of catalase and ascorbate peroxidase decreased during the aging process. Moreover, nutrient analysis showed that a high magnesium level in the cultivar bestowed greater resilience to deterioration, which can indicate a potential function of magnesium in the cell structure via reflex in seed aging through seed respiration.