No abstract

Population projections based on life tables and stage-specific consumption rates can reveal the stage structure and damage potential of the pest population. Our results showed that monitoring data obtained by using pheromone traps were not in concordance with the damage potential of the pest population. This approach offers a promising tool for pest management.

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).

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.

No abstract