Eucalyptus rust is caused by the biotrophic fungus, Austropuccinia psidii, which affects commercial plantations of Eucalyptus, a major raw material for the pulp and paper industry in Brazil. In this manuscript we aimed to uncover the molecular mechanisms involved in rust resistance and susceptibility in Eucalyptus grandis. Epifluorescence microscopy was used to follow the fungus development inside the leaves of two contrasting half-sibling genotypes (rust-resistance and rust-susceptible), and also determine the comparative time-course of changes in metabolites and proteins in plants inoculated with rust. Within 24 h of complete fungal invasion, the analysis of 709 metabolomic features showed the suppression of many metabolites 6 h after inoculation (hai) in the rust-resistant genotype, with responses being induced after 12 hai. In contrast, the rust-susceptible genotype displayed more induced metabolites from 0 to 18 hai time-points, but a strong suppression occurred at 24 hai. Multivariate analyses of genotypes and time points were used to select 16 differential metabolites mostly classified as phenylpropanoid-related compounds. Applying the Weighted Gene Co-Expression Network Analysis (WGCNA), rust-resistant and rust-susceptible genotypes had, respectively, 871 and 852 proteins grouped into 5 and 6 modules, of which 5 and 4 of them were significantly correlated to the selected metabolites. Functional analyses revealed roles for photosynthesis and oxidative-dependent responses leading to temporal activity of metabolites and related enzymes after 12 hai in rust-resistance; while the initial over-accumulation of those molecules and suppression of supporting mechanisms at 12 hai caused a lack of progressive metabolite-enzyme responses after 12 hai in rust-susceptible genotype. This study provides some insights on how E. grandis plants are functionally modulated to integrate secondary metabolites and related enzymes from phenylpropanoid pathway and lead to temporal divergences of resistance and susceptibility responses to rust.

The aims of this study were to determine the potential of S4 super sweet corn inbred lines for hybrid synthesis, identify the predominant types of gene action and correlations among different traits, significant for breeding programs. The 81 hybrids obtained from a partial diallel 9x9 and three checks were evaluated. A complete randomized block design, with three replicates, and two sowing seasons was used. We could notice significant hybrid effects, general combining ability (GCA) of GI and GII groups and specific combining ability (SCA) in relation to evaluated traits, highlighting the existence of hybrids with superior performance and the expression of additive and non-additive effects. The inbred lines: L1, L3, L6 and L9 (GI) and L1’, L7’ and L9’ (GII) showed the best GCA and SCA estimates, being present in the nine selected hybrids with superior and competitive performance in relation to the checks. The estimated correlations indicate that, for a breeding program aiming to increase grain productivity, evaluating, at least, the dehusked ears, prioritizing genotypes with larger ear diameters and longer ear lengths is important.

The objective of this work was to determine the possibility of haploid induction in tropical supersweet corn (Zea mays L. var. saccharata) using a maternal inducer, as well as to identify alternative methods for haploid selection. A single-cross hybrid of field corn and 11 tropical supersweet corn populations were crossed with the haploid inducer. The haploids were pre-selected using the R1-navajo marker and were differentiated into haploids or false positives at the V2-V3 stage, based on the color of the first leaf sheath and on the length of stomata guard cells. The obtained results are indicative of the possibility of inducing maternal haploids in populations of tropical supersweet corn. However, a large number of false-positive haploids were incorrectly selected by the R1-navajo marker. The color of the first leaf sheath was efficient for haploid identification in supersweet corn populations, and the method based on stomata morphometry can be used when there is no color distinction on the first leaf sheath.

Pyrostegia venusta is usually found in the secondary growth of the Atlantic forests, and in the Brazilian Savanna. Flowers and leaves of this plant are used in folk remedies for treating a wide variety of healthy conditions, this way is important evaluate its safety and antioxidant potential for this applications. For this, was made a ethanolic extract from its flowers and analyzed with toxicological, genotoxicity and antioxidant tests, the toxicological analysis was made by reproductive toxicity in rats and clatogenicity/aneugenicity in human lymphocytes. The genotoxicity was studied by micronucleus test mice bone marrow. The antimutagenic test in root cells of Allium cepa, the antioxidant assays used was DPPH, FRAP, Lipid Perxidation and REM, beyond of that the extract was analyzed in HPLC showing the profile of its compounds. The toxicological analysis showed that P. venusta has no negative significant effect on reproductive and cellular level. The micronucleus test in mouse bone marrow, the extract protected cells from cyclophosphamide, mutagenic compound, in a similar way. The A. cepa test showed that the extract reduced chromosomal disorders formations. The antioxidant activity of extract was significant, except in REM test. The phytochemical analysis showed the presence of flavonoids compounds. P. venusta extract does not present reproductive toxicity and genotoxic effects. However, the extract of this species showed antigenotoxic and antioxidant potential, possibly due to the different flavonoid compounds present in its extract.