Immature survival and development of alfalfa weevil, Hypera postica (Gyllenhal) (Coleoptera: Curculionidae), were examined at 15 constant temperatures ranging from 9 to 37 degrees C. At 9 and 37 degrees C, eggs did not develop. Embryos developed to adulthood between 11.5 and 36 degrees C, although survival was low at both ends of the temperature range. Distribution of development times for all stages of alfalfa weevil were skewed toward longer times mainly at moderate temperatures. Constant proportion of time spent in egg, larva, and pupa indicated rate isomorphy within the range 14-31.5 degrees C. No significant difference was shown between development time of males and females at any of the temperatures tested. Two linear and 23 nonlinear models were fitted to describe development rate of immature stages of H. postica as a function of temperature, as well as estimating the thermal constant and critical temperatures (i.e., T(min), T(opt), and T(max)). There was no statistical difference between the estimated parameters, using Ikemoto and ordinary linear methods. Of the nonlinear models fitted, the Logan-6/Lactin-2, Analytis-3/Briere-2, and Analytis-3/Briere-2 models were found to be the best for modeling development rate of egg, larva, and entire immature stages of H. postica, respectively. Our findings will be incorporated in more efficient phenological models of this pest and its population dynamics.

Alfalfa weevil, Hypera postica (Gyllenhal) (Coleoptera: Curculionidae), is among the most destructive pests of alfalfa, Medicago sativa L., in the world. Survivorship and fecundity schedules of H. postica were investigated to characterize the population growth potential of the weevil at six constant temperatures: 11.5, 14.0, 19.0, 24.0, 29.0, and 31.5 degrees C. Preoviposition period, oviposition period and female longevity significantly decreased with rising temperature within the temperature range tested. At the respective temperatures adult female lived an average of 294.2, 230.2, 163.6, 141.0, 84.10, and 32.9 d, with average lifetime progeny production of 470, 814, 2209, 3619, 2656, and 338 eggs per female. The net reproductive rates (R0) were 86.9, 288.0, 869.7, 1,479.7, 989.8, and 107.8 females per female, respectively. Mean daily fecundity (Mx) was modeled as a function of time by using both Enkegaard and Analytis models. Survivorship data (l(x)) of adult females were summarized and compared using the shape and scale parameters of the Weibull frequency distribution model across the temperature range tested. Life table entropy values within the range 14.0-31.5 degrees C (H < 0.5) indicates Slobodkin's type I survivorship curve; however, the value of 0.806 at 11.5 degrees C (H > 0.5) corresponds to type III. As temperature increased, the r(m) exhibited an asymmetrical dome-shaped pattern, with a maximum value of 0.114 females per female per d at 29.0 degrees C. The r(m)-temperature relation of weevils was modeled and critical temperatures (T(Min), T(Opt), and T(Max)) for intrinsic rate of increase of the weevil were computed as 8.83, 30.61, and 32.14 degrees C and 5.72, 29.94, and 32.12 degrees C by using Analytis/Allahyari and Analytis/Briere-2 models, respectively.

Key factors are those causes that are most responsible for the observed changes in population density between generations. Stage‐frequency of alfalfa weevil was modeled using Manly‐1997 model. Multiple decrement life table parameters from an 8 year‐field study were analyzed using traditional and λ contribution methods. In traditional method, the key factor was determined as kLII, the death of period‐two larvae from all mortality factors, whereas in λ contribution method, the key factor was determined as b2&3, oviposition rate of females per square meter. These differences result directly from the sensitivity of the population growth rate, λ, to variation of both k and b in various stages of the weevil. Among all mortality factors, only kLI‐Z, the death of period‐one larvae from the entomopathogenic fungus, Zoophthora phytonomi (Arthur) Batko (Zygomycetes: Entomophthoraceae), kLII and kLII‐Z, the death of period‐two larvae from Z. phytonomi, acted in a density dependent fashion. Remaining factors were independent of population densities affected. Using λ contribution method, life table approach still remains a major way of studying the dynamics of field populations for applied ecologists and population managers.