Germination and field emergence are delayed and their duration is prolonged due to the declining soil temperature during the spring season, which is reflected in the subsequent stages of crop growth, therefore, this study aimed to improve germination. Under a wide range of environmental conditions, a laboratory factorial experiment was carried out to study the effect of seed stimulation with potassium nitrate (distilled water only (0), 2, 4, and 6 mg L-1) and with an aqueous extract of licorice roots (distilled water only (0), 3, 6, and 9 g L-1) on the seed viability and vigor. The laboratory experiment was carried out according to the Completely Randomized Design (CRD) with four repetitions. The results showed the superiority of the interaction treatment between the two concentrations 6 gm L-1 and 6 mg L-1 for each of licorice root extract and potassium nitrate by giving the highest average of the final germination 99%, the seedling vigor index reached 3846, the germination percentage at accelerating age test of 75%, and the germination percentage at the cold test of 76%. We can conclude that there was a response to soaking the seeds in licorice root extract at specific concentrations, with a clear response to potassium nitrate, and the response could be better when soaking in potassium nitrate at concentrations higher than 6 mg L-1. We also recommend that the soaking duration in any of the two factors is 18 hours to improve germination under a wide range of environmental conditions.
Two simple methods for the determination of eugenol were developed. The first depends on the oxidative coupling of eugenol with p-amino-N,N-dimethylaniline (PADA) in the presence of K3[Fe(CN)6]. A linear regression calibration plot for eugenol was constructed at 600 nm, within a concentration range of 0.25-2.50 μg.mL–1 and a correlation coefficient (r) value of 0.9988. The limits of detection (LOD) and quantitation (LOQ) were 0.086 and 0.284 μg.mL–1, respectively. The second method is based on the dispersive liquid-liquid microextraction of the derivatized oxidative coupling product of eugenol with PADA. Under the optimized extraction procedure, the extracted colored product was determined spectrophotometrically at 618 nm. A l
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