Effects of nano Fe/SiO2 fertilizers on germination and growth of barley and maize

Iron (Fe) nanoparticles (NPs), with 30–40 nm diameter, were stabilized on sand. The resulting synthesized Fe/SiO₂ NPs, with different Fe contents (0–25 mg kg^?1) were employed as fertilizers in probing the mean germination time (MGT), growth and dry matter of barley and maize and their comparison with common Fe/SiO₂ in a completely randomized design (CRD) experiment. The results showed that our fertilizers had significant effects on MGT, with the lowest of 0.58 day for barley and 0.79 day for maize; at 15 and 5 mg kg^?1 nano Fe/SiO₂, respectively. Application of 15 mg kg^?1 of nano Fe/SiO₂ increased the shoot length: 8.25% and 20.8% for barley and maize, respectively. However, the concentration of 25 mg kg^?1 had a negative impact on shoot length in barley. Increasing the concentrations of both nano and common Fe/SiO₂ particles, increased the root lengths in both plants, however this increase was higher with the application of nano Fe/SiO₂. Likewise, seedling length enlarged with the concentration increase of both Fe/SiO₂ particles and was more pronounced with nano Fe/SiO₂. The application of nano Fe/SiO₂ was more effective compared with the common Fe/SiO₂ in encouraging barley and maize growth. The positive impact was higher in maize than barley.     

Mapping connectivity and conflict risk to identify safe corridors for the Persian leopard

Landscape Ecology - Many large carnivores depend on habitat patches outside protected areas, as well as safe corridors between them. However, corridor assessments typically ignore potential...     

A Novel Splice Site Variant in the LDLRAP1 Gene Causes Familial Hypercholesterolemia

Background:FH, a hereditary disorder, is caused by pathogenic variants in the LDLR, APOB, and PCSK9 genes. This study has assessed genetic variants in a family, clinically diagnosed with FH. Methods:A family was recruited from MASHAD study in Iran with possible FH based on the Simon Broom criteria. The DNA sample of an affected individual (proband) was analyzed using WES, followed by bioinformatics and segregation analyses. Results:A novel splice site variant (c.345-2A>G) was detected in the LDLRAP1 gene, which was segregated in all affected family members. Moreover, HMGCR rs3846662 g.23092A>G was found to be homozygous (G/G) in the proband, probably leading to reduced response to simvastatin and pravastatin. Conclusion:LDLRAP1 c.345-2A>G could alter the PTB, which acts as an important part of biological pathways related to lipid metabolism. Key Words: Genetic research, LDLRAP1, Hypercholesterolemia, Hydroxymethylglutaryl-CoA Reductase Inhibitors