To provide a comprehensive evaluation of walnut cultivar resistance to the dusky-veined walnut aphid, Panaphis juglandis (Goeze), we collected the life table data of this aphid reared on five cultivars of walnut (‘Akça I,’ ‘Chandler,’ ‘Fernette,’ ‘Fernor,’ and ‘Pedro’) under field conditions. The raw data of the developmental time, survival rate, and fecundity was analyzed using the age-stage, two-sex life table to account for the variable developmental rate and stage differentiation among individuals. Due to the species’ longer immature developmental time, shorter adult longevity, shorter reproduction period, and lower fecundity, the net reproduction rate (R₀ = 5.9 offspring), intrinsic rate of increase (r = 0.0983 d⁻¹), and finite rate (λ = 1.1034 d⁻¹) were the lowest when aphids were reared on the Fernor cultivar, while those reared on Akça I exhibited the highest population parameters (R₀ = 18.0 offspring, r = 0.2031 d⁻¹, and λ = 1.2252 d⁻¹). Based on the population characteristics, Fernor is a less favorable cultivar for the development and reproduction of P. juglandis. We also demonstrated the advantages of using bootstrapping for the analysis of standard errors of developmental time, longevity, fecundity, and other parameters as well. Our results indicated that demographic analysis of pest development, survival, and reproduction based on the age-stage, two-sex life table offers a comprehensive assessment of pest growth potential on different crop cultivars.

To better understand the predator–prey relationship and to compare predation rates, we studied the life table and predation rate of the predator Eocanthecona furcellata Wolff (Hemiptera: Pentatomidae) when reared on two major crucifer pests, Spodoptera litura (F.) (Lepidoptera: Noctuidae) and Plutella xylostella L. (Lepidoptera: Plutellidae). The net reproductive rate, intrinsic rate of increase, finite rate, and net predation rates of E. furcellata reared on P. xylostella were 292.4 offspring, 0.1389 d⁻¹, 1.1490 d⁻¹, and 644.1 third instars of P. xylostella, respectively. These values are significantly higher than those reared on S. litura, i.e., 272.3 offspring, 0.1220 d⁻¹, 1.1298 d⁻¹, and 863.1 third instars of S. litura. To evaluate the predation potential of E. furcellata fed on P. xylostella and S. litura, we combined both the growth rate and predation rate to calculate the finite predation rate (ω); our results showed that E. furcellata is an effective predator of both S. litura (ω = 1.6029) and P. xylostella (ω = 1.4277).

Population growth parameters of the Dysaphis pyri (Boyer de Fonscolombe) (Hemiptera: Aphididae) were evaluated on four different cultivars (Coscia, Ankara, Williams, and Santa-Maria) of pear (Pyrus communis L.) under field conditions in the Van region of Turkey. Aphids were kept on leaves of 10-yr-old pear trees in Plexiglas clip-cells (20 mm in diameter and 10 mm in height, with the upper side covered with muslin). For the description of the stage differentiation during population growth, we analyzed raw data of developmental time, survival, and fecundity using the age-stage, two-sex life table to take the variable developmental rate among individuals into account. Results indicated that the Coscia and Ankara cultivars are less favorable hosts for D. pyri because of the longer preadult developmental time, higher preadult mortality rate, and lower total fecundity on these cultivars. The intrinsic rate of increase (r), the net reproduction rate (R₀), and the finite rate of increase (λ) values were lower on the Coscia and Ankara cultivars. We discussed the application of the Weibull function, polynomial model, and Enkegaard model in life table studies. Because these models are often inaccurate in describing survival and reproduction parameters, we suggest that their application in life table research should be reevaluated.

Tetranychus urticae Koch is a cosmopolitan pest whose rapid developmental rate enables it to produce colonies of thousands of individuals within a short time period. When a solitary virgin female colonizes a new host plant, it is capable of producing male offspring through the arrhenotokous parthenogenesis; once her sons mature, oedipal mating occurs and the female will produce bisexual offspring. To analyze the effect of arrhenotokous reproduction on population growth, we devised and compared separate life tables for arrhenotokous and bisexual populations of T. urticae using the age-stage, two-sex life table theory. For the cohort with bisexual reproduction, the intrinsic rate of increase (r), finite rate (λ), net reproductive rate (R₀), and mean generation time (T) were 0.2736 d⁻¹, 1.3146 d⁻¹, 44.66 offspring, and 13.89 d, respectively. Because only male eggs were produced during the first 8 d of the oviposition period and the cohort would soon begin bisexual reproduction, it would be theoretically wrong to calculate the population parameters using the survival rate and fecundity of an arrhenotokous cohort. We demonstrated that the effect of arrhenotokous reproduction could be accurately described and evaluated using the age-stage, two-sex life table. We also used population projection based on life table data, quantitatively showing the effect that arrhenotokous reproduction has on the growth potential and management of T. urticae.