The maximum mortality rate (81.67%) was recorded at 10,000 IJs/kg soil 7 days post treatment (Fig. 3c).
The maximum mortality rate (100%) for CcAgNPs was observed at 20 mg/l and 25 mg/l for A. aegypti and A. stephensi vectors respectively, while highest percent of mortality for SnAgNPs was noticed in both A. aegypti and A. stephensi at 25 mg/l.
Cervical cancer mortality, usually occurring among unscreened women, increases with age, with the maximum mortality rate reported for white women between age 45 years and 70 years, and for black women in their 70s [ 38, 39].
The prey population evolves to reduce defense (x decreases) when m increases, because at a stable equilibrium, the right-hand side of d x/d t in eqn (1) becomes negative with decreased P. Prey evolution therefore increases, the maximum predator mortality rate at which the predator population is viable; this increase in is the quantitative contribution of indirect evolutionary rescue.
In these tables also the minimum and maximum observed number of deaths and the minimum and maximum observed CHD mortality rates per 100,000 (number of deaths/population) were presented for every identified period.
The maximum likelihood estimates of mortality rates (lower and upper confidence intervals) were obtained by fitting the data to a Logistic model and are based on pooled data for each sex and treatment.
Data describing annual (2004 2015) age frequencies (0 1 to 5 6 years), yield, effort (boat-days), and average weights at age were used to fit various stochastic models to estimate mortality rates by maximum likelihood.
Life-history traits tested are wood density (WD), maximum tree size (D950.1), and mortality rates for trees ≥ 10 cm DBH (MD10 and RGRD10, respectively).
