Functional responses of immature stages of Propylea quatuordecimpunctata (L.) to varying densities of Aphis fabae Scopoli
reared on Vicia faba L. were evaluated under laboratory conditions. All larval stages of the predator were starved for 12 h prior
to being placed individually for 24 h in plastic containers with different densities of its prey, A. fabae, on potted V. faba plants.
Logistic regression analysis of the proportion of aphids consumed as a function of initial density indicated that all larval instars of P.
quatuordecimpunctata exhibited a type II functional response when searching for A. fabae on V. faba plants. Attack rates (0.059,
0.057, 0.065 and 0.064) and handling times (6.18, 2.37, 1.06 and 0.44) for first to fourth instar larvae, respectively, were estimated
using Holling’s disc equation.
A number of aphid species have been shown to produce winged dispersal morphs in the presence of natural enemies. Previous studies tested specialized aphid predators such as ladybirds or lacewing larvae. We confronted colonies of pea aphids with the polyphagous rove beetles, Drusilla canaliculata and Tachyporus hypnorum. For both predators we found that the percentage of winged morphs increased in predator-attacked pea aphid colonies compared to a control. The behaviour of the two rove beetles species was noticeably different. D. canaliculata mostly foraged on the ground and rarely on the plant, while T. hypnorum was almost exclusively observed on the plants, causing a higher number of aphids to drop to the ground, which resulted in a stronger increase in winged morph production. Our results clearly show that not only monophagous aphid predators but also more polyphagous insect predators, which include aphids in their diet, can induce aphids to produce winged morphs., Adalbert Balog, Mohsen Mehrparvar, Wolfgang W. Weisser., and Obsahuje seznam literatury
While the study of colour patterns is a traditional subject of evolutionary ecology, there are various hypotheses which suffer from a lack of experimental evidence. One intriguing possibility is a trade-off between warning efficiency and detectability. After a certain size threshold, the detrimental effect of increased detectability can outweigh the benefits of warning colouration. One may thus expect corresponding patterns at the level of ontogenetic development: as juveniles grow, they should first acquire warning colouration, and then lose it again. We analysed this possibility in Orgyia antiqua, a moth species with hairy larvae which are polyphenic with respect to the intensity of warning colouration. We detected a regular change in colour patterns through larval life. Indeed, the larvae tend to display warning colouration at intermediate sizes while dull colours dominate in fully grown larvae. In aviary experiments, we confirmed that the colourful phenotype is the one that causes the strongest aversion in birds. Nevertheless, the effect was rather weak and most of the larvae were still eventually consumed when found. Unexpectedly, for human subjects, the warningly coloured larvae were harder, and not easier to find among natural vegetation, most likely due to the disruptive effect of the aposematic colour pattern. Importantly, the trend was reversed in the largest size class, suggesting that the disruptive colouration loses its advantage as the larva grows. This is consistent with the actual patterns of size-dependence of colouration. We present evidence against an alternative explanation which relates size-related change in colouration to behavioural changes prior to pupation. We conclude that even if the efficiency of the warning effect plays a role in determining the size-dependence of colouration, the pattern may be largely explained by the effects of size-dependent detectability alone.
Pea aphids (Acyrthosiphon pisum) have been reported to produce winged offspring in the presence of predatory ladybirds. These offspring may leave host plants by flight after they have developed into winged adults. The inter-generational nature of this response raises the question about the chances of survival of aphids developing in attacked colonies. We studied the behaviour of predatory ladybirds on host plants by releasing adult 7-spot ladybirds (Coccinella septempunctata) on bean plants hosting either no prey individuals or colonies of 10 or 30 pea aphids. Interactions between predator and prey were recorded until the ladybird left the plant. Ladybird patch residence time increased with the number of aphids present on a plant but beetles generally left a plant before all aphids were eaten. The time budget of the ladybirds revealed a high proportion of time not spent in feeding activities. Predation rate was about one aphid killed per 10min residence time in both treatments with aphid-infested plants. Aphids that survived an attack by the predator or that were alarmed when a conspecific was attacked often emigrated from the host plant, and their number was of the same magnitude as the number of aphids killed by the predator. On average, pea aphid numbers at the end of an experiment were reduced to less than a third of the initial value. The results of the experiment show that attack by single ladybirds does on average not cause immediate extinction of small aphid colonies. The short patch residence times of on average less than two hours show that a predator individual that induces winged-offspring production in an aphid colony will not any longer be present in the colony when the induced offspring mature. To understand the adaptiveness of predator-induced wing development in pea aphids the probabilities of subsequent attacks on an aphid colony need to be investigated.