Diallel analysis among 16 maize populations adapted to the northern U.S. Corn Belt for grain yield and grain quality traits

Genetically diverse germplasm is needed to increase frequency of favorable alleles of economically important traits in maize improvement. The objectives of this study were to determine the genetic components involved in grain yield and grain quality traits, and provide preliminary assessment of useful heterotic groups and patterns from a large sample of maize populations adapted to the northern U.S. Corn Belt. Sixteen populations were used in the diallel mating design following Gardner–Eberhart Analysis II to estimate variety (v _i ) and heterosis (h _ij ) genetic effects for grain yield and grain quality traits. Specific heterosis (s _ij ) and predicted means of population crosses for grain yield were used to evaluate the heterotic relationships among the populations. Data for grain yield and grain quality traits were generated in partially balanced single lattice experiments across North Dakota (ND) locations in 2010, 2011, and 2012. Analyses of variance showed significant differences among genotypes. Heterosis effects explained most of the differences among diallel entries for grain yield, while v _i effects had greater influence on grain quality traits. NDL, EARLYGEM 21c, NDSCD(FS-CS)C2, NDSS, and NDSM(M-FS)C9 were identified as elite populations for grain quality improvement. NDSS × NDBS22(R-T1)C9 and NDBS1011 × EARLYGEM 21c showed high s _ij effects for grain yield with good grain quality. NDSS and EARLYGEM 21c represent stiff stalk synthetic (SSS) group, and NDBS1011 fall under non-SSS group. Further studies need to validate the heterotic group of NDBS22(R-T1)C9. Recurrent and pedigree selection programs will be established for selected populations and population crosses to integrate pre-breeding with cultivar development.     

Effects of habitat degradation on the abundance, richness and diversity of raptors across Neotropical biomes

Population growth and human development result in biodiversity loss and biological homogenization not only in developed countries, but increasingly in the less developed countries as well. In those countries, where urbanization and agricultural intensification occur at a faster rate than in developed countries, habitat degradation appears to be the leading cause of wildlife loss. During the breeding seasons of 2002–2005 we conducted road surveys across five biomes of Argentina to detect variations in raptor community attributes as potential indicators of broad scale habitat degradation. Abundance of individuals, richness and diversity of species were calculated to assess the effects of habitat transformation and patch size on these community attributes. Raptor communities strongly varied in relation to habitat transformations, with lower abundance of individuals, richness and diversity of species in more transformed landscapes. Small patches of natural vegetation and locations in which natural and cultivated lands where interspersed showed lower richness and diversity of raptors than large patches. Fragmentation was the main cause of reductions in abundance of individuals. Although the relative contribution of our two estimates of habitat degradation to abundance, richness and diversity of raptors varied among biomes, these community attributes proved useful as predictors of habitat degradation. This was especially true in habitats where raptor communities are more complex although overall patterns remained constant across biomes, from forests to deserts. Taking into account current trends of habitat transformation (drastic increments in monocultures, urban areas, and habitat patchiness), the conservation of raptor communities in these biomes could be seriously compromised. In terms of species-specific responses of raptors to habitat degradation, a rapid process of homogenization can be expected, resulting in only a few winner species within a general scenario of losers.     

Relationship Between Soft Wheat Flour Physicochemical Composition and Cookie‐Making Performance

Nowadays in Argentina, cookies, crackers, and cakes are made of flour obtained from bread wheat with additives or enzymes that decrease the gluten strength but increase production costs. The present research work aims to study the relationship between flour physicochemical composition (particle size average [PSA], protein, damaged starch [DS], water soluble pentosans [WSP], total pentosans [TP], and gluten), alkaline water retention capacities behavior, solvent retention capacities profile (SRC) and cookie‐making performance in a set of 51 adapted soft wheat lines with diverse origin to identify better flour parameters for predicting cookie quality. Cookie factor (CF) values were 5.06–7.56. High and significant negative correlations between sucrose SRC (–0.68), water SRC (–0.65), carbonate SRC (–0.59), and CF were found, followed by lactic SRC that presented a low negative but significant correlation (r = –0.35). The flour components DS (r = –0.67), WSP (r = –0.49), and TP (r = –0.4) were negatively associated to CF. PSA showed a negative correlation with CF (r = –0.43). Protein and gluten were the flour components that affected cookie hardness, but no significant correlation were found with pentosan or DS content. A prediction equation for CF was developed. Sucrose SRC, PSA, and DS could be used to predict 68% of the variation in cookie diameter. The cluster analysis was conducted to assess differences in flour quality parameters among genotypes based on CF. Clusters 1 and 4 were typified by lower CF (5.70 and 5.23, respectively), higher DS, pentosan content, and SRC values. Cluster 2 with a relative good CF (6.47) and Cluster 3 with the best cookie quality, high CF (7.32) and low firmness, and the lowest DS, TP, WSP content, and sucrose SRC values.     

Different isolates from Leishmania braziliensis complex induce distinct histopathological features in a murine model of infection

The aim of this study was to evaluate the histopathological features in tissues of mice infected by human isolates (I, II, and III) or the reference M2903 strain of Leishmania braziliensis complex. BALB/c and C57Bl/6 mice were infected in the hind footpad with 10⁶ stationary-phase promastigotes of L. braziliensis complex. The evolution of lesions was observed for 10 weeks and the animals were then euthanized and liver, spleen and popliteal lymph nodes were collected. Tissues were stained with hematoxylin and eosin and analyzed by immunohistochemistry assay. Increased thickness of infected footpads was observed in all animals, lesions were nodular and non-ulcerated. Mice infected with isolate I presented inflammatory infiltrates consisting predominantly of mononuclear cells in all tissues examined, and also a great number of megakaryocytes, compared with other isolates. Infection with isolate II led to an infected footpad enlargement not seen in other isolates. In addition, mononuclear infiltrates in the liver and hemosiderin in spleen were noted. Conversely, mice infected with either isolate III or M2903 strain only showed an increased number of megakaryocytes in spleen. All tissues examined had detectable amastigote forms of Leishmania by immunohistochemistry in all groups. Taking together, our results showed an unforeseen behavior of different isolates of L. braziliensis complex that led to diverse pathological findings.     

Prevalence of Rickettsia species antibodies and Rickettsia species DNA in the blood of cats with and without fever

Rickettsia species antibodies have been detected in some cats but it is unknown whether infected cats develop clinical signs. The prevalence of Rickettsia species deoxyribonucleic acid (DNA) in blood from clinically ill cats has not been determined. The objective of this study was to determine if cats with fever (body temperature >or=102.5 degrees F [39.2 degrees C]) were more likely to have evidence of rickettsial infection than healthy, age-matched, control cats with a body temperature<102.5 degrees F. Rickettsia species polymerase chain reaction (PCR) assays were performed to detect rickettsial DNA extracted from blood (71 paired samples), indirect immunofluorescence assays (IFA) were performed to detect serum antibodies against Rickettsia felis (90 paired samples) and Rickettsia rickettsii (91 paired samples), and the results between pairs were compared. All samples were negative for Rickettsia species DNA. More cats with fever were seropositive for R felis or R rickettsii than control cats, but results were not statistically significant. Results of this pilot study failed to show an association between Rickettsia species DNA or Rickettsia species antibodies and fever.