To date, there has been little agreement on supporting the hypothesis that how some key vegetative traits of camelina (Camelina sativa (L.) Crantz var. 'Soheil') are dependent on plant biomass. Therefore, the main aim of this investigation was to quantify the relationship between the size of camelina plants and seed production across a broad-range of plant densities through modelling approaches. To make a wide range of plant densities, a fan design was used in eight replicates in an experimental field at Sari Agricultural Sciences and Natural Resources University, Iran. To quantify the relation between plant density and other plant traits, a regression analysis was carried out and the coefficient of determination (R 2 ) was considered to evaluate the goodness of fit model. A power model (y = ax b ) could describe well the relationship between plant density (ranged 113-2905 plants m À2 ) and plant biomass, seed production, number of seeds per plant, stem diameter, and siliques number, with the coefficient of determination (R 2 ) values of 0.85, 0.87, 0.65, 0.64, and 0.90, respectively. The harvest indexes were 13.8%-26.9%, depending on plant density. Seed production per plant was positively correlated to the siliques number (r = 0.85), the branch number (r = 0.80), and the seed number (r = 0.99) which could be key components of camelina seed production per plant. Furthermore, no significant correlation was found among plant height, thousand-seed weight, and harvest index with seed production per plant. In conclusion, plant biomass could be considered an important trait to predict plant growth models of camelina. Also, a lower plant density of camelina can be compensated by a greater number of siliques, branches and seeds per plant.

Quantification of germination niches under salt stress, temperature, and their interaction using population-based threshold models is important to predict seedling emergence patterns. Seeds of Sarcocornia fruticosa, Sarcocornia alpini, and Salicornia emerici were treated with various temperatures at different NaCl concentrations. Results indicated that the median base NaCl concentration was roughly steady (0.68, 0.73, and 0.70M, respectively) at sub-optimal temperature, then decreased linearly at supra-optimal temperature until the ceiling temperature (Tc). The estimated base, optimum and ceiling temperatures, in water, were − 0.5, 15 and 29°C for Sarcocornia fruticosa, − 2.5, 11 and 24°C for Sarcocornia alpini, and 9.5, 25 and 40°C for Salicornia emerici, respectively. At all species, the base temperature has not changed with the salinity while both optimum and ceiling temperatures decreased. Also, Salicornia emerici showed rapid and synchronized germination when salinity decreases during the rainy season coinciding with favorable temperatures compared with other species.