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
Macrolophus pygmaeus (Hemiptera: Miridae) is an important predator of pests of horticultural crops and here its ability as a predator of Acyrthosiphon pisum (Hemiptera: Aphididae) is addressed for the first time. The percentage predation of the different aphid instars and the number partially consumed were studied. Our results, obtained using choice and no-choice tests, revealed that M. pygmaeus caught and consumed more young than later instars of A. pisum, which confirms results of previous studies using other species of aphids. We also studied the interactions between predators (male/female) foraging in the same patch. When the prey/predator ratio is kept constant at 10 : 1 the average percentage of aphids completely consumed by individual females or males does not change with increase in the number of foraging predators. However, the number of partially consumed aphids decreased when females shared the same patch. In contrast, there was an increase in the number of aphids partially consumed when two males shared the same patch. The results were discussed in terms of potential predator foraging strategies since intraspecific competition is a key factor modulating the dynamics of prey-predator systems., Juliana Durán Prieto, Vincenzo Trotta, Paolo Fanti, Cristina Castañé, Donatella Battaglia., and Obsahuje bibliografii
1_The respiratory metabolism of different polyphenic forms of the pea aphid, including wingless and winged asexual females (virginoparae), sexual females (oviparae) and winged or wingless adult males, was investigated using a micro-respirographic method. The records revealed sub-nanoliter amounts per min of O2 consumption or CO2 output. Respiratory metabolism of individuals was monitored for 3 to7 h after removal of the aphid from the food plant. Most of the recordings were for relatively large (3.5 mg), wingless asexual females (virginoparae). These aphids exhibited a continuous and very regular respiratory gas exchange (example: specimen of 3.5 mg body mass consumed 180 nl of O2 per min; released simultaneously 300 nl CO2 per min; = standard metabolic rate of 3085 µl O2 / g / h; R.Q. = 1.66). This continuous pattern of respiration occurred only when the aphids were kept at relatively high humidity. By contrast, aphids of various seasonal forms exhibited discontinuous respiratory gas exchange when kept in relatively dry air (atmospheric, room conditions). These patterns can be briefly described as follows: (a) Short and rather small micro-cycles of CO2 emission, manifested usually by the sudden expiration of 60–120 nl of CO2 once every 5 min; (b) Larger bursts of 240–480 nl of CO2 with a periodicity of one hour; (c) Enormously large, discontinuous bursts of 10–14 µl CO2, duration 10–30 min, repeated with a periodicity of several hours. There was no constant pattern of diffusive CO2 emission (DGC). The aphids exhibited a pattern of CO2 release that was appropriate for the external conditions, such as temperature and humidity, and internal physiological conditions such as metabolic activity, availability of reserve substances (carbohydrate, lipid) and water. Certain stages (wingless virginoparae) exhaled volumes of CO2 greatly in excess of their O2 consumption (R.Q. over 1.5)., 2_Sudden exhalations of CO2 from the body were a consequence of a bulk production and outflow of CO2 and not due to the diffusion of CO2 previously accumulated within the tracheal system. Due to their generally high metabolic activity (1142 to 6780 µl O2 / g / h), aphid tissue and organs produced relatively large amounts of metabolically formed carbonic acid. The resulting respiratory acidaemia was moderated by outbursts of gaseous CO2, liberated from liquid carbonate buffers by a regulatory mechanism based on enzymatic hydration and neutralization of carbonic acid by discontinuous formation of gaseous CO2., Karel Sláma, Pavel Jedlička., and Obsahuje seznam literatury
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.