Mutual interference involves direct interactions between individuals of the same species that may alter their foraging success. Larvae of aphidophagous coccinellids typically stay within a patch during their lifetime, displaying remarkable aggregation to their prey. Thus, as larvae are exposed to each other, frequent encounters may affect their foraging success. A study was initiated in order to determine the effect of mutual interference in the coccinellids’ feeding rate. One to four 4th larval instars of the fourteen-spotted ladybird beetle Propylea quatuordecimpunctata were exposed for 6 hours into plastic containers with different densities of the black bean aphid, Aphis fabae, on potted Vicia faba plants. The data were used to fit a purely prey-dependent Holling type II model and its alternatives which account for interference competition and have thus far been underutilized, i.e. the Beddington-DeAngelis, the Crowley-Martin and a modified Hassell-Varley model. The Crowley-Martin mechanistic model appeared to be slightly better among the competing models. The results showed that although the feeding rate became approximately independent of predator density at high prey density, some predator dependence in the coccinellid’s functional response was observed at the low prey—high predator density combination. It appears that at low prey densities, digestion breaks are negligible so that the predators do waste time interfering with each other, whereas at high prey densities time loss during digestion breaks may fully accommodate the cost of interference, so that the time cost may be negligible.
Functional response models are important in understanding predator-prey interactions. The development of functional response methodology has progressed from mechanistic models to more statistically motivated models that can account for variance and the over-dispersion commonly seen in the datasets collected from functional response experiments. However, little information seems to be available for those wishing to prepare optimal parameter estimation designs for functional response experiments. It is worth noting that optimally designed experiments may require smaller sample sizes to achieve the same statistical outcomes as non-optimally designed experiments. In this paper, we develop a model-based approach to optimal experimental design for functional response experiments in the presence of parameter uncertainty (also known as a robust optimal design approach). Further, we develop and compare new utility functions which better focus on the statistical efficiency of the designs; these utilities are generally applicable for robust optimal design in other applications (not just in functional response). The methods are illustrated using a beta-binomial functional response model for two published datasets: an experiment involving the freshwater predator (an aquatic insect) preying on (a small crustacean), and another experiment involving a ladybird beetle ( L.) preying on the black bean aphid ( Scopoli). As a by-product, we also derive necessary quantities to perform optimal design for beta-binomial regression models, which may be useful in other applications.
The effect of temperature on the development, survival, longevity, and fecundity of the 14-spotted ladybird beetle, Propylea quatuordecimpunctata L. (Coleoptera: Coccinellidae) reared on bean aphid, Aphis fabae Scopoli (Hemiptera: Aphididae) was determined at six constant temperatures (17, 20, 25, 30, 32.5, and 35 ± 1°C) in the laboratory. Results showed a temperature—dependent development of the coccinellid. An appropriate linear model indicated that 218.0 degree days above a threshold of 10.2°C were needed to complete immature development from egg to adult emergence. Data were fitted to the nonlinear Briere model, which for total immature period estimated the upper developmental threshold at 36.0°C, the lower threshold at 12.2°C and the temperature for maximum developmental rate at 30.3°C. Survival of immature stages varied significantly across temperatures with the lowest survival of just 14% occurring at 32.5°C and the highest (96%) at 25°C. In addition temperature showed a profound effect on female longevity over this viable range of temperatures, as it decreased from 123.06 d at 17°C to 33.53 d at 30°C. The highest fecundity (724.6 eggs/female) was recorded at 25°C. These results might be useful tools for the prediction of P. quatuordecimpunctata phenology and the interaction with its prey.
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