Open Access
How to translate text using browser tools
1 September 2013 Shallot Aphids, Myzus ascalonicus, in Strawberry: Biocontrol Potential of Three Predators and Three Parasitoids
Annie Enkegaard, Lene Sigsgaard, Kristian Kristensen
Author Affiliations +

The parasitization capacity of 3 parasitoids and the predation capacity of 3 predators towards the shallot aphid, Myzus ascalonicus Doncaster (Homoptera: Aphididae), on strawberry, Fragaria x ananassa Duchesne (Rosales: Rosaceae) cv. Honeoye, were examined in laboratory experiments. In Petri dish assays, both Aphidius colemani Viereck (Hymenoptera: Aphidiidae) and A. ervi Haliday readily stung shallot aphids, with no significant difference in stinging frequency between the two species. A. ervi induced a significantly higher mortality (79.0 ± 7.2%) in terms of stung aphids compared with A. colemani (55.3 ± 4.1%); however, only a minor fraction (2.7 ± 1.8% and 7.1 ± 3.1%, respectively) of the killed aphids resulted in formation of mummies, presumably due to a physiological response to parasitism. The low percentage of mummification precludes the use of either Aphidius species in anything but inundative biocontrol. In similar set-ups, Aphelinus abdominalis (Dalman) (Hymenoptera: Aphelinidae) killed almost half (49.6 ± 5.3%) of the exposed aphids through host feeding. In addition, 23.2 ± 7.3% of non-host-fed aphids developed into mummified aphids, and 38.1 ± 13.2% of non-host-fed aphids died from other parasitoid-induced causes. However, the host feeding rate was reduced to only 1.2 ± 0.8%, and no significant parasitization mortality was observed on strawberry plants, suggesting that host plants interfered with A. abdominalis activity. This parasitoid does not, therefore, seem to be suited to either inoculative or inundative biocontrol of shallot aphids in strawberry. The three predators studied were the green lacewing, Chrysoperla carnea Steph. (Neuroptera: Chrysopidae), the two-spotted lady beetle, Adalia bipunctata L. (Coleoptera: Coccinellidae), and the gall midge Aphidoletes aphidimyza (Rondani) (Diptera: Cecidomyiidae). Third instars of all 3 predators readily preyed upon the shallot aphid in Petri dish set-ups with significant differences in daily predation (34.62 ± 3.45, 25.25 ± 3.18, and 13.34 ± 1.45, respectively). Further studies on A. bipunctata revealed that the larvae maintained their daily predation capacity (32.0 ± 6.3) on strawberry plants. About 60% of already ovipositing A. bipunctata refrained from laying any eggs on the first day after transfer to set-ups with combinations of shallot or peach-potato aphids, Myzus persicae (Sulzer) (Homoptera: Aphididae), and strawberry or sweet pepper leaves. The aphid species and the plant species did not, however, have a significant influence on the number of females laying eggs, the average number of eggs laid during the first day being 6.37±1.28 per female. Adult lady beetles had a significant preference for odor from controls without plants over odors from uninfested strawberry or pepper plants, but they showed no preference for either of the plant species, whether infested with aphids or not. The predation capacity of A. bipunctata on shallot aphids holds promise for its use in inundative biocontrol, and the results on egg laying cues suggests that inoculative biocontrol may be possible, although further studies will be needed for a complete evaluation.


Strawberry, Fragaria × ananassa Duchesne (Rosales: Rosaceae), is the most important high-value berry crop in Denmark for fresh consumption (Danmarks Statistik 2005; Nielsen 2006). Danish strawberry is prone to infestations with a number of pest species, e.g., the strawberry tortrix moth, Acleris comariana, the strawberry blossom weevil, Anthonomus rubi, the strawberry mite, Phytonemus pallidus, and the two-spotted spider mite, Tetranychus urticae (Lindhardt et al. 2003). In addition, new strawberry pest species known to cause serious problems in warmer climates (Karl 1983; Cross et al. 1994; Rabasse et al. 2001) are beginning to appear. One of these species is the shallot aphid, Myzus ascalonicus Doncaster (Homoptera: Aphididae), which can be expected to become an increasing problem in Denmark due to the global climate changes.

Aphids have not previously posed a serious problem in Danish strawberry grown in open fields or in tunnels. However, in 2008, M. ascalonicus infestations were observed in Denmark and Sweden in plastic-covered strawberry beds (Petersen et al. 2008). M. ascalonicus, known to attack strawberry in Germany (Borchardt 1958; Martin Hommes, Julius Kuehn Institute, Federal Research Centre for Cultivated Plants, Germany personal communication) and the United Kingdom (Cross et al. 1994; Anonymous 2011), can inflict serious damage on this crop due to its induction of malformed leaves, stunted growth, and shortened and distorted flower stalks (Anonymous 2011). There are indications that shallot aphids can become especially problematic in strawberry if temperatures in February and March are above normal (Hurst 1969). Winters in Denmark are expected to become milder as a consequence of global climate changes; combined with elevated temperatures during production due to the ongoing shift in strawberry cultivation methods (from open field to plastic-covered beds or in tunnels) (Daugaard 2005), this is likely to increase the importance of M. ascalonicus as a pest in Danish strawberry. To forestall the accompanying increase in the use of insecticides, it is important to develop biological control methods against this pest.

The literature presents only a few investigations on natural enemies of M. ascalonicus (Wahab 1985; Wahab and Askew 1989); however, more information exists regarding natural enemies of the strawberry aphid, Chaetosiphon fragaefolii (e.g., Easterbrook et al. 2006; Fitzgerald 2006). In addition, countless investigations have been made regarding the possibilities of biological control of other aphid species in various field and, especially, greenhouse crops. A number of aphidophagous natural enemies have welldocumented beneficial effects and are commercially available. However, these natural enemies are not necessarily effective against M. ascalonicus, which may not be included in the host or prey range of the natural enemy, may not occupy accessible spatial niches, or may display effective defense behavior (Enkegaard and Brødsgaard 2002). Consequently, this study screened a number of commercially available benificials for their predation or parasitization capacity towards M. ascalonicus, and further studies were undertaken with better-suited candidate species.

Materials and Methods

The experiments were conducted at light and temperature conditions mimicking those found in spring in Danish tunnel strawberry. For an overview of experiments, see Table 1.

Plants, insects

Onion plants, Allium cepa L. (Asparagales: Alliaceae) cv. Stutgarter Riesen, strawberry plants, and sweet pepper plants, Capsicum annuum L. (Solanales: Solanaceae) cv. Arcano, were grown separately in insect-proof netcovered cages (68 × 75 × 82 cm) in a climatecontrolled greenhouse compartment at 23 ± 1° C, 70 ± 5% RH and 16:8 L:D at Research Centre Flakkebjerg, Aarhus University, Denmark.

M. ascalonicus were received from the Julius Kuehn Institute, Federal Research Centre for Cultivated Plants, Braunschweig, Germany, and used to initiate a rearing. M. ascalonicus were reared in cages at environmental conditions as described above. Peach-potato aphids, Myzus persicae (Sulzer) (Homoptera: Aphididae), were obtained from a long-standing colony reared on sweet pepper and maintained at the Research Centre Flakkebjerg in similar cages and conditions.

Natural enemies (parasitoids Aphidius colemani Viereck (Hymenoptera: Aphidiidae), A. ervi Haliday, and Aphelinus abdominalis (Dalman) (Aphelinidae)), predators (lacewings, Chrysoperla carnea Steph. (Neuroptera: Chrysopidae), lady beetles, Adalia bipunctata L. (Coleoptera: Coccinellidae), and gall midges, Aphidoletes aphidimyza (Rondani) (Diptera: Cecidomyiidae)) were purchased from natural enemies producers EWH BioProduction ( and Borregaard Bioplant (

The parasitoids were supplied as mummies, which were placed according to species in open Petri dishes (diameter: 9 cm) placed in a small cage (30.5 × 22 × 15 cm) in a climate cabinet (23 ± 1° C, 70 ± 1% RH, 16:8 L:D) until emergence. The parasitoids were allowed to mate in the cage for 1 day with access to sugar water, after which females were sexed under a stereo-microscope and used for experimentation.

Gall midges were supplied as third instars and used directly in the experiments. Lacewings and lady beetles were supplied as second instars. For all experiments, except those mentioned below, larvae were reared individually in Petri dishes (diameter: 5.5 cm) to the third instar on surplus flour moth, Ephestia kuehniella Zeller (Lepidoptera: Pyralidae), eggs in a climate cabinet at similar conditions as above. One day prior to experimentation, predator larvae were starved for 24 hr by keeping them individually in Petri dishes in a climate cabinet in the same conditions as above.

For the behavioral experiment and the experiment with egg laying of A. bipunctata, the rearing of the purchased second instars continued until adulthood, after which emerged adults were kept together in groups of 15–20 individuals of similar age. Both males and females were kept together to ensure mating. A. bipunctata were fed on flour moth eggs, with a supplemental feeding of grain aphids, Sitobion avenae (F.) (Homoptera: Aphididae), every two days. For the egg-laying experiment, adult A. bipunctata were collected one day prior to experimentation and placed individually in small Petri dishes with the same food. The following day, females that had laid eggs during isolation were used for experimentation. For the behavioral experiments, adult A. bipunctata were collected 1 day prior to experimentation and placed individually in small Petri dishes without food but with access to water. After a 24-hr starvation period, the lady beetles were used for experimentation.

Screening experiments

Parasitoids. A set-up used successfully in prior experiments (e.g., Enkegaard and Brødsgaard 2002) was originally intended for the screening experiments with parasitoids. In this Petri dish set-up, aphids were exposed on detached leaves to a female parasitoid for a pre-defined period depending upon the parasitoid species; they were then left for ≈1.5 weeks, after which the degree of parasitization was recorded. After several attempts, this design had to be abandoned because M. ascalonicus were unable to survive on detached strawberry leaves for the period needed for development of visible signs of parasitization. Instead, the following experiments were undertaken:

Aphidius colemani and Aphidius ervi. For recording frequency of parasitization, Petri dishes (diameter: 9 cm) with moistened filter paper and a detached strawberry leaf (≈ 4 × 7 cm) with 25 second instar M. ascalonicus were each supplied to a mated female parasitoid and observed under a stereo microscope for 15 min in a climate-controlled greenhouse compartment at 18 ± 1° C. The number of aphids stung was recorded. The number of replicates was 13 and 15 for A. colemani and A. ervi, respectively. For recording actual parasitization of stung aphids, similar Petri dishes with similarly sized aphid-infested strawberry leaves were each supplied to a mated female parasitoid and observed under a stereo microscope in the same greenhouse compartment at 18 ± 1° C. For each individual parasitoid (replicate), 10 aphid nymphs observed to be stung were immediately transferred to a small, 3leafed, potted onion plant (≈ 10 cm height), which was subsequently placed in a climate cabinet (23 ± 1° C, 70 ± 1% RH, 16:8 L:D) for 1.5 weeks, after which the respective number of live, dead, and mummified aphids was recorded. The number of replicates was 13 A. colemani and 10 A. ervi. In addition, 5 onion plants, each with 10 second instar M. ascalonicus unexposed to parasitoids, were set up as controls.

Aphelinus abdominalis. Petri dishes (diameter: 9 cm) with similarly sized aphid-infested strawberry leaves as above were each supplied to a mated female parasitoid and placed for 24 hr in a climate cabinet (18 ± 1° C, 70 ± 1% RH, 12:12 L:D), after which the numbers of dead and live aphids were recorded. For each replicate, the live aphids were, as above, subsequently transferred to a small potted onion plant placed at similar conditions and recorded in a similar fashion after 1.5 weeks. The number of replicates was 16, with 5 controls consisting of onion plants with 25 second instar M. ascalonicus unexposed to parasitoids.

Predators. For the screening experiments, a similar set-up as above was used. The Petri dishes were each supplied with a starved third instar predator and placed in a climate cabinet (18 ± 1° C, 70 ± 1% RH, 12:12 L:D). After 3 hr (C. carnea), 4 hr (A. bipunctata), or 24 hr (A. aphidimyza), the predator was removed and the number of consumed aphids recorded. The predation times for each predator species were defined based on the predators’ maximum daily predation capacity. The number of replicates was 25 for C. carnea, 25 for A. bipunctata, and 23 for A. aphidimyza. In addition, controls (n = 10) without natural enemies were used for each predator species.

Further studies of the most suited predator and parasitoid species

Aphelinus abdominalis. Experiments were conducted to examine the parasitization/host feeding potential of A. abdominalis on whole strawberry plants. Small cages (23 × 23 × 23 cm) with either a small 3- to 4-leafed potted strawberry plant or a small 4- to 6-leafed potted sweet pepper plant with 60 second instar M. ascalonicus were each supplied with 1 female A. abdominalis (mated, maximum 2 days old). After 24 hr in a climate cabinet (18 ± 1° C, 70 ± 1% RH, 12:12 L:D), the parasitoids were removed and the number of dead aphids recorded. For each replicate, the live aphids were subsequently transferred to a small potted onion plant (dimension as above) and placed in a climate cabinet (23 ± 1°C, 70 ± 1% RH, 16:8 L:D) for 1.5 weeks, after which the respective number of live, dead, and mummified aphids was recorded. The number of replicates was 11 for strawberry and 20 for sweet pepper. In addition, plants with 60 second instar M. ascalonicus unexposed to parasitoids were made as controls for each plant species (n = 10 for strawberry and n = 13 for sweet pepper).

Adalia bipunctata predation on whole plants. Predation by A. bipunctata larvae was studied on whole plants. Similar cages as above with similarly sized aphid-infested strawberry or sweet pepper plants were each supplied with one third instar A. bipunctata larva (starved for 24 hr). After 24 hr in a climate cabinet (18 ± 1° C, 70 ± 1% RH, 12:12 L:D), the larvae were removed and the number of consumed aphids recorded. The number of replicates was 12 and 14 for set-ups with strawberry plants and sweet pepper plants respectively. In addition, controls without A. bipunctata larvae were made for each plant species (n = 6 for strawberry and n= 8 for sweet pepper).

Adalia bipunctata egg laying cues. Experiments were conducted to examine if ovipositing A. bipunctata would obtain sufficient cues from aphid-infested strawberry to continue egg laying. Petri dishes (diameter: 9 cm) with moistened filter paper and either a strawberry leaf or a sweet pepper leaf infested with either M. ascalonicus or M. persicae (≈ 100 aphids per leaf) were each supplied with 1 adult, 6–7-day-old, female A. bipunctata. After 24 hr in a climate cabinet (18 ± 1° C, 70 ± 1% RH, 12:12 L:D), the females were removed and the number of eggs counted. The number of replicates was 15 for each treatment.

Adalia bipunctata behavior. The reaction of adult A. bipunctata to odor emitted from uninfested and aphid-infested leaves was examined in a still-air olfactometer set-up modified after Weeks et al. (2010). The set-up consisted of a rectangular plastic box (5 × 21 × 31 cm) with the edges sealed with parafilm and with two holes (4 cm diameter, covered with insect net) at the bottom, each hole positioned at opposite ends of the box on the longest central axis and 25 cm apart. A small glass container (3 L) was placed to contain test material under each hole. The top of the container was sealed against the box with isolation tape. A single adult A. bipunctata, less than 1 week old and starved for 24 hr, was introduced to the center of the set-up through a small hole (1 cm diameter) in the center of the box lid. The hole was plugged, and the beetle was then observed for 5 min, during which time the time spent in each of the two halves of the box was recorded. Individuals that remained inactive for more than 2 successive minutes were discarded from the analysis. Only 2 individuals were discarded. Six experiments were conducted to examine the response of A. bipunctata to small 3-leafed (8–10 cm height) uninfested or aphid-infested sweet pepper or strawberry plants in the following treatment combinations: (1) uninfested strawberry plant versus empty container, (2) uninfested sweet pepper plant versus empty container, (3) uninfested strawberry plant versus uninfested sweet pepper plant, (4) aphidinfested strawberry plant versus empty container, (5) aphid-infested sweet pepper plant versus empty container, (6) aphid-infested strawberry plant versus aphid-infested sweet pepper plant. The infested material was produced by adding approximately 50 M. persicae (mainly nymphs) to the plants 2 days prior to experimentation. The plants were placed in a climate cabinet (23 ± 1° C, 70 ± 1% RH, 16:8 L:D) until use. The test material was placed in the containers 5 min prior to initiation of the experiment. Three batches of 5 A. bipunctata were tested for each treatment.

As is common practice in olfactometer studies (e.g., Souissi et al. 1998; Venzon et al. 1999), after testing each batch of insects the set-up was cleaned with 70% alcohol and left to dry for 5 min. Subsequently, odor sources were switched between the left and right side to minimize any spatial effect on choices. Each individual was tested only once. The experiments were conducted in a darkened room (23° C) with a light source positioned directly above the center of the set-up.

Data analysis

The recorded predation was corrected for the mortality in the corresponding controls (Abbott 1925). For comparison between the three predators, the corrected predation rates were extrapolated to daily consumption (assuming predation for 12 hr of light). The number of stung, dead, and mummified aphids in the screening experiments with A. colemani and A. ervi was analyzed in one-way ANOVA with the species as fixed effects. The corrected number of dead aphids in the Petri dish screenings of A. abdominalis, C. carnea, A. aphidimyza, and A. bipunctata was analyzed in one-way ANOVA with the species as fixed effects. Because the variance depended on the species in question, a separate variance was estimated for each species. Similar analysis was applied for the whole plant experiments with A. abdominalis and A. bipunctata. The egg-laying of A. bipunctata was analyzed in one-way ANOVA with the four combinations of aphids and plants as fixed effects. In order to examine the behavior, the differences in time spent in the two halves of the set-up were analyzed in one-way ANOVA with pairs of treatment as fixed effects. The comparison of the two different materials in each pair was examined by testing the hypothesis that the difference was zero (this analysis is similar to a paired t-test except that in this analysis the variance was assumed to be the same for all pairs). All analyses were performed using procedures glm, mixed, and glimmix of SAS (SAS Institute Inc. 2008).

Results and Discussion

Table 1 shows an overview of the experiments, and Table 2 shows a summary of the results.


Screening of parasitization capacity for Aphidius colemani and Aphidius ervi. Both Aphidius species readily stung M. ascalonicus, which is in contrast to a previous study undertaken with a strain of M. ascalonicus (obtained from Campanula, called “Campanula-strain”) with a strongly developed defensive behavior towards parasitization by both Aphidius species (Enkegaard and Brødsgaard 2002). The average number of stung aphids (± SE) was not significantly different (F1,27 = 0.48, p = 0.785) between the two parasitoid species, being 6.8 ± 2.4 and 6.1 ± 1.2 for A. colemani and A. ervi respectively. Not surprisingly, a high proportion of aphids that had been stung by either species died within 1.5 weeks. The average mortality (± SE) induced in aphids stung by A. ervi (79.0 ± 7.2%) was significantly higher than the mortality induced in aphids stung by A. colemani (55.3 ± 4.1%) (F1, 22 = 9.22, p = 0.0063). However, only a minor fraction (7.1 ± 3.1% and 2.7 ± 1.8% for A. colemani and A. ervi respectively) of the aphids killed after exposure to either of the parasitoids died as a result of a completed parasitization process leading to formation of mummies, with no significant difference between these values (F1,22 = 1.20, p = 0.268).

Parasitization by the two parasitoid species leading to fully developed mummies has been reported in the literature to vary from 40 to 80% at temperatures above 20° C, depending upon the offered aphid host species, host density, and environmental conditions (e.g., Sequeira and Mackauer 1994; van Steenis 1995; Takada and Tada 2000; Zamani et al. 2007; Byeon et al. 2010). These rates, expressing mortality among all exposed aphids (i.e., not just stung aphids), are higher than the rates for mummification found in our study, indicating that the performance of A. colemani and A. ervi against M. ascalonicus on strawberry is far from optimal. The low degree of mummification suggests a physiological response to parasitism by Aphidius parasitoids in M. ascalonicus, as demonstrated for clones of pea aphids, Acyrthosiphonpisum, to parasitization by A. ervi (Henter and Via 1995), although the physiological mechanism described by Henter and Via (1995) served as a true defense (i.e., survival) reaction, which was not the case in our study, because the stung aphids actually died. It therefore seems that M. ascalonicus has the potential to form clones with resistance to parasitization based on physiological or behavioral mechanisms (Enkegaard and Brødsgaard 2002).

Even though the overall mortality rates induced in stung M. ascalonicus were quite high, the low degree of mummification precludes the use of either species in anything but inundative biocontrol in which no reproduction of significance can be expected. Given a choice, A. ervi should be preferred due to its higher mortality induction.

Aphelinus abdominalis: screening for parasitization capacity and parasitization on whole plants. Contrary to the 2 Aphidius species, A. abdominalis uses its hosts for host feeding (Stary 1988; Haardt 1990), as evidenced in the present experiment with almost half (49.6 ± 5.3%) of the aphids being killed within 24 hr after exposure to the parasitoids.

In addition, A. abdominalis inflicted additional mortality to M. ascalonicus, with 23.2 ± 7.3% of the non-host-fed aphids developing into mummified aphids, and 38.1 ± 13.2% of the non-host-fed aphids dying from parasitoidinduced causes; this was presumably a result of parasitizations that did not develop to the mummified stage.

The results found for A. abdominalis are in contrast to the study by Enkegaard and Brødsgaard (2002) in which the defensive behavior of the Campanula strain of M. ascalonicus was obstructive to parasitization by A. abdominalis. On the other hand, our findings agree with the study of Wahab (1985) in which dissections of M. ascalonicus 3 days after exposure to A. abdominalis at 18° C revealed that 40–70% of the aphids contained parasitoid eggs or larvae. The method used by Wahab (1985) allowed for neither determination of mortality due to host-feeding nor determination of the proportion of parasitized aphids that would eventually have mummified. However, in view of reports on successful aphid biocontrol with A. abdominalis (e.g., Hurni and Stadler 1993; Colombo and Fasce 1994; Blumel and Hausdorf 1996), it seems probable that the majority of the parasitized aphids in the study of Wahab (1985) would have mummified. The lower degree of mummification found in our study was therefore likely a reflection of the presumed physiological mechanism mentioned above for the Aphidius species.

Aphelinus abdominalis and A. ervi inflicted the same overall mortality on M. ascalonicus (about 80%), although the mortality inflicted by the latter was based only on stung aphids. The mortality to be expected among a group of exposed M. ascalonicus would thus be higher for A. abdominalis, which, combined with its ability to reproduce on this aphid species, at first would seem to make it a better candidate for biological control with the potential to be used as an inoculative agent. However, the results from the experiment on realization of the potential of A. abdominalis on whole plants showed otherwise.

On whole plants, the host feeding mortality inflicted by A. abdominalis on M. ascalonicus was significantly influenced by the host plant species (p < 0.0001, F1,29 = 38.45), with a corrected host feeding mortality (± SE) of 32.1 ± 5.3% on sweet pepper and only 1.2 ± 0.8% on strawberry. Compared with the relatively high host feeding mortality observed on strawberry leaves, the latter result suggests that qualities pertaining to whole strawberry plants were obstructive to A. abdominalis activity. Contrary to the results obtained in the screening experiment, no significant parasitization mortality was observed in the whole plant set-up with either of the host plants (strawberry: ñ = 0.73, F1,20 = 0.12; sweet pepper: p = 0.83, F1,32 = 0.05). Thus, the obstructive factors pertained to both host-feeding and parasitization activities. It may be speculated that the trichomes of strawberry plants constituted an obstacle for parasitoid search, which primarily is based on walking since this species seldom flies (Biobest 2011). Another possibility is that volatile signals emitted from shallot aphid-infested strawberry plants were in some way discouraging to the parasitoids (Mölck et al. 1999; Mölck and Wyss 2003). On sweet pepper, the occurrence of host feeding but the lack of parasitization was surprising because an obstructive influence from either plant structure (other than trichomes because sweet pepper is void of trichomes (Madadi et al. 2007)) or pest-plant volatiles would have been expected to affect both behavioral elements more or less equally.

Even though A. abdominalis may have some potential to control shallot aphids on sweet pepper, the same potential is not likely on strawberry when used in an inundative fashion.


Screening of predation capacity. Third instar larvae of all 3 predators readily preyed upon M. ascalonicus, with a significant difference (F2, 70 = 19.34, p < 0.0001) in daily predation between predator species. The average daily predation rates (± SE) of larvae of A. aphidimyza, A. bipunctata, and C. carnea were 13.34 ± 1.45, 25.25 ± 3.18, and 34.62 ± 3.45, respectively. These results are within the range of predation rates reported on various aphid species for A. bipunctata (Timms et al. 2008; Jalali et al. 2009a), C. carnea (Athhan et al. 2004; Montoya-Alvarez et al. 2010), and A aphidimyza (Morse and Croft 1987; Kulp et al. 1989; Harizanova and Ekbom 1997). C. carnea larvae were more voracious than larvae of both A. bipunctata (t70 = -2.00, p = 0.0498) and A. aphidimyza (t70 = -5.68, p < 0.0001), and A. bipunctata larvae were more voracious than A. aphidimyza larvae (t70 = 3.40,p = 0.0011).

Predation by Adalia bipunctata on whole plants. Third instar A. bipunctata had significantly higher predation (F1,24 = 14.17, p < 0.001) on M. ascalonicus on sweet pepper (average daily corrected number eaten (± SE) = 56.3 ±1.7) than on strawberry (32.0 ± 6.3), with the latter predation rate being in accordance with that observed in the screening experiment. Contrary to the situation with A. abdominalis, the change in experimental dimensions did not seem to be obstructive to the activity of the A. bipunctata larvae. However, the difference in predation on the 2 host plant species showed that larvae were influenced by prey-plant characteristics (Timms et al. 2008; Alhmedi et al. 2010), perhaps due to the structure or texture of the plants (Banks 1957; Shah 1982; Carter et al. 1984).

Egg laying cues for Adalia bipunctata. A high proportion of the already ovipositing A. bipunctata refrained from laying any eggs during the 24 hr experimental period (strawberry-M. ascalonicus: 46.6%, strawberry-M. persicae: 53.3%, sweet pepper-M. ascalonicus: 66.7%, sweet pepper-M. persicae: 66.7%). The number of females refraining from egg-laying was, however, not affected by the species of the aphid and the species of the plant (χ2 = 0.038, df = 1,p = 0.845). The results are in accordance with the study by Hemptinne et al. (2000), which demonstrated that female A. bipunctata use cues other than those associated with aphids or plants in their oviposition site selection.

The average number (± SE) of eggs laid per day by A. bipunctata was similar, irrespective of aphid and plant species (F1,59 = 1.07, p = 0.369), with the following values attained in each plant-aphid system: 8.67 ± 3.08 eggs (strawberry-M. ascalonicus), 8.07 ± 2.91 eggs (strawberry-M. persicae), 5.93 ± 2.59 eggs (sweet pepper-M. ascalonicus), and 2.8 ± 1.24 eggs (sweet pepper- M. persicae). Since the A. bipunctata in this experiment were only allowed a short egg-laying period with the new prey, the average daily egg laying across all treatments (6.37 ± 1.28) was, not surprisingly, lower than reported in other studies where egg production was observed for longer periods (16–20 eggs) (Hamalainen et al. 1975; Ware et al. 2008; Jalali et al. 2009b). Further studies will be needed to examine if the proportion of egg layers as well as the egg-laying capacity of A. bipunctata would increase after longer exposure to M. ascalonicus on strawberry.

Behavior of Adalia bipunctata. The time spent by adult A. bipunctata over the different odor sources of uninfested and aphid-infested plant material is shown in Table 3. A. bipunctata had a significant preference for clean air from the empty container over odors from uninfested strawberry (trial 1), and there was a tendency for a similar preference for clean air over uninfested sweet pepper (trial 2). This apparent repellency of both plant species is in accordance with the findings of Timms et al. (2008), who found a significant negative olfactory response of adult A. bipunctata to uninfested Norway spruce compared to controls without plants. However, the results contradict previous observations that adult A. bipunctata are not attracted to volatiles from uninfested broad beans, rape, or mustard (Francis et al. 2004), or to volatiles from uninfested broad bean or Nasturtium plants (Raymond et al. 2000). Avoidance or attraction of A. bipunctata to plant volatiles apparently depends upon the plant species in question. When A. bipunctata was given a choice between both uninfested plant species (trial 3), neither was preferred, as was also the case when they were given a choice between both infested plant species (trial 6). However, the presence of aphids made both plant species more attractive since A. bipunctata no longer displayed a significant preference for clean air (comparison of trials 1 and 4 and of trials 2 and 5). Still, only trials 1 and 4 showed a tendency to being significantly different (t = -1.86, p = 0.066), whereas this was not the case for trials 2 and 5 (t = -1.35, p = 0.189). This result is in accordance with the findings of Raymond et al. (2000), who observed a tendency for A. bipunctata with previous feeding experience to show an olfactory preference for broad bean or Nasturtium plants infested with black bean aphids, Aphis faba, over uninfested plants.

Although A. bipunctata seems to find strawberry an inferior host plant compared to sweet pepper, its realized predation capacity on M. ascalonicus on strawberry indicates a potential in inundative biocontrol. In addition, the results on eg- laying cues suggest that A. bipunctata may be used in inoculative biocontrol strategies, provided that adults developing from released larvae will remain in the culture to initiate further generations. Even though A. bipunctata is apparently repelled by uninfested strawberry, the extent of this reaction in the presence of aphids suggests that this may indeed be the case. It might consequently be expected that adult A. bipunctata developing from released larvae will remain in aphidinfested strawberries. It would be valuable to investigate if short-term learning processes, as has been documented for the seven-spotted lady beetle, Coccinella septempunctata (Glinwood et al. 2011), in adult A. bipunctata developing from larvae released in a strawberry culture may increase their tendency to remain in the crop.


This study has demonstrated that the reproductive success of A. colemani, A. ervi, and A. abdominalis is low on M. ascalonicus compared to the abilities of these parasitoids on other aphid species. The low reproductive success is not a result of behavioral defense reactions towards the parasitoids. Instead, M. ascalonicus seemingly responds physiologically to the internal presence of parasitoid eggs or larvae, although this reaction does not serve as an effective defense mechanism as demonstrated in other aphid species (Henter and Via 1995), since the aphids themselves die. The very low reproductive success of the two Aphidius species precludes their use in biocontrol against M. ascalonicus in strawberry except for purely inundative releases. In addition, the reduced host- feeding and reproductive capacity of A. abdominalis on whole strawberry plants compared to the initial screening experiments likewise precludes the use of this species even as an inundative agent. Whether other parasitoid species than the 3 species examined here will be able to parasitize M. ascalonicus on whole strawberry plants remains to be seen. It likewise remains to be seen if other M. ascalonicus populations will exhibit the same resilience to parasitization as seen here.

All predator larvae readily preyed upon M. ascalonicus on strawberry, with C. carnea larvae being the most voracious. Although A. bipunctata seems promising as a biocontrol agent, as judged from its predation capacity and its ability (at least for about half of the females) to lay eggs on M. ascalonicusinfested strawberries, further studies are needed to examine its departing tendencies in strawberry. Furthermore, studies are needed on realized fertility, development, and survival for individuals feeding continuously on M. ascalonicus. At the same time, it would be interesting to further examine the two other predators, especially C. carnea, to clarify the realization of their predation potential under more realistic conditions.

Table 1.

Overview of experiments.


Table 2.

Summary of the average (± SE) values for the different biological characteristics examined for the 3 parasitoids (Aphidius colemani, Aphidius ervi, Aphelinus abdominalis) and 3 predators (Aphidoletes aphidimyza, Chrysoperla carnea, Adalia bipunctata) with shallot aphids, Myzus ascalonicus, as host/prey. NS: mortality was not significantly different from the controls.


Table 3.

Average time (± SE) (in sec) over the different odor sources in the 6 treatment combinations, as well as the test statistics for differences in preference between the two odor sources.



This project was supported by the Danish Environmental Protection Agency. Dr. Martin Hommes, Julius Kuehn Institute, Federal Research Centre for Cultivated Plants, Germany, is thanked for supplying shallot aphids. Technician Gitte Christiansen, Dept. of Agroecology, Aarhus University, is thanked for technical assistance in connection with the experiment and Kirsten Jensen, Dept. of Agroecology, Aarhus University, for editorial and language assistance. In addition, three anonymous reviewers are thanked for their helpful and constructive comments to a previous version of this paper.



WS Abbott. 1925. A method of computing the effectiveness of an insecticide. Journal of Economic Entomology 18(2): 265–267. Google Scholar


A Alhmedi , E Haubruge , F Francis. 2010. Identification of limonene as a potential kairomone of the harlequin ladybird Harmonia axyridis (Coleoptera: Coccinellidae). European Journal of Entomology 107(4): 541–548. Google Scholar


Anonymous. 2011. Shallot aphid, Myzus ascalonicus. Rothamsted Insect Survey. Available online: Google Scholar


R Athhan , B Kaydan , MB Özgökce. 2004. Feeding activity and life history characteristics of the generalist predator, Chrysoperla carnea (Neuroptera: Chrysopidae) at different prey densities. Journal of Pest Science 77(1): 17–21. Google Scholar


CJ Banks. 1957. The behaviour of individual coccinellid larvae on plants. The British Journal of Animal Behaviour 5(1): 12–24. Google Scholar


Biobest. 2011. Biological control: Beneficial insects and mites: Aphelinus-System. Biobest. Available online: Google Scholar


S Blumel , H Hausdorf. 1996. Greenhouse trials for the control of aphids on cut-roses with the chalcid Aphelinus abdominalis Dalm (Aphelinidae, Hymen). Anzeiger für Schädlingskunde 69(3): 64–69. Google Scholar


G Borchardt. 1958. Über das Freilandvorkommen von Myzus ascalonicus Doncaster. Nachrichtenblatt der Deutschen Pflanzenschutzdienst (Braunschweig) 10(1): 9–10. Google Scholar


YW Byeon , M Tuda , JH Kim , MY Choi. 2010. Functional responses of aphid parasitoids, Aphidius colemani (Hymenoptera: Braconidae) and Aphelinus asychis (Hymenoptera: Aphelinidae). Biocontrol, Science and Technology 21(1): 57–70. Google Scholar


MC Carter , D Sutherland , AFG Dixon. 1984. Plant structure and the searching efficiency of coccinellid larvae. Oecologia 63(3): 394–397. Google Scholar


M Colombo , D Fasce. 1994. Integrated control of spring crops of tomato in protected cultivation. Informatore Agrario 50(29): 37–41. Google Scholar


JV Cross , AM Berrie , M Ryan , A Greenfield. 1994. Progress towards integrated plant protection in strawberry production in the UK. Brighton Crop Protection Conference: Pests and Diseases, 1994 3: 725–730. Google Scholar


Danmarks Statistik. 2005. Statistikbanken. Danmarks Statistik. Available online: Google Scholar


H Daugaard. 2005. To ugers tidligere høst af jordbær i tunnel. Frugt og Grønt 4(4): 150– 151. Google Scholar


MA Easterbrook , JD Fitzgerald , MG Solomon. 2006. Suppression of aphids on strawberry by augmentative releases of larvae of the lacewing Chrysoperla carnea (Stephens). Biocontrol Science and Technology 16(9): 893–900. Google Scholar


A Enkegaard , HF Brødsgaard. 2002. “Resistance” towards biological control. IOBC/wprs Bulletin 25(1): 65–68. Google Scholar


F Francis , G Lognay , E Haubruge. 2004. Olfactory responses to aphid and host plant volatile releases: (E)-beta-farnesene an effective kairomone for the predator Adalia bipunctata. Journal of Chemical Ecology 30(4): 741–755. Google Scholar


JD Fitzgerald. 2006. Biological control of thrips and aphids in runnel-grown strawberry in UK. IOBC/wprs Bulletin 29(9): 21–26. Google Scholar


R Glinwood , E Ahmed , E Qvarfordt , V Ninkovic. 2011. Olfactory learning of plant genotypes by a polyphagous predator. Oecologia 166(3): 637–647. Google Scholar


H Haardt. 1990. Study on the significance of host feeding in the aphid parasitoid Aphelinus abdominalis (Dalm.). Mitteilungen aus der Biologischen Bundesanstalt für Land- und Forstwirtschaft, Berlin-Dahelem 266: 323. Google Scholar


M Hamalainen , M Markkula , T Raji. 1975. Fecundity and larval voracity of four ladybeetle species (Col., Coccinellidae). Annales Entomologici Fennici 41(4) : 124–127. Google Scholar


V Harizanova , B Ekbom. 1997. An evaluation of the parasitoid, Aphidius colemani Viereck (Hymenoptera: Braconidae) and the predator Aphidoletes aphidimyza Rondani (Diptera: Cecidomyiidae) for biological control of Aphis gossypii Glover (Homoptera: Aphididae) on cucumber. Journal of Entomological Science 32(1): 17–24. Google Scholar


J-L Hemptinne , M Doumbia , AFG Dixon. 2000. Assessment of patch quality by ladybirds: the role of aphid and plant phenology. Journal of Insect Behaviour 13(3): 353–359. Google Scholar


HJ Henter , S Via . 1995. The potential for coevolution in a host-parasitoid system. I. Genetic variation within an aphid population in susceptibility to a parasitic wasp. Evolution 49(3): 427–438. Google Scholar


B Hurni , E Stadler. 1993. The parasitic wasp Aphelinus abdominalis against aphids in tomatoes. Gemuse 29(3): 196–198. Google Scholar


GW Hurst. 1969. Shallot aphid in Southeast England. Plant Pathology 18(2): 62–66. Google Scholar


MA Jalali , L Tirry , P De Clercq. 2009a. Food consumption and immature growth of Adalia bipunctata (Coleoptera: Coccinellidae) on a natural prey and a factitious food. European Journal of Entomology 106(2): 193–198. Google Scholar


MA Jalali , L Tirry , P De Clercq. 2009b. Effects of food and temperature on development, fecundity and life-table parameters of Adalia bipunctata (Coleoptera: Coccinellidae). Journal of Applied Entomology 133(8): 615–625. Google Scholar


E Karl. 1983. Observations on the occurence of Myzus ascalonicus Donc, on cultivated strawberries and various weed species. Nachrichtenblatt für den Pflanzenschutz in der DDR 37(11): 219–221. Google Scholar


D Kulp , M Fortmann , M Hommes , H-P Plate. 1989. Die räuberische Gallmücke Aphidoletes aphidimyza (Rondani) (Diptera: Cecidomyiidae): ein bedeutender Blattlausprädator; Nachschlagewerk zur Systematik, Verbreitung, Biologie, Zucht und Anwendung. Mitteilungen aus der Biologischen Bundesanstalt für Land- und Forstwirtschaft, BerlinDahlem 250. Google Scholar


H Lindhardt , N Elmegaard , M Strandberg , K Paaske , B Løschenkohl , B Melander , SL Nielsen , LM Hansen , Jensen P Krüger , D Yohalem , H Daugaard , M Bengtsson . 2003. Vurdering af muligheder for forebyggelse og alternativ bekæmpelse i frugt og baer. Bilag 4 til rapporten ““Muligheder for forebyggelse og alternativ bekæmpelse indenfor gartneri og frugtavl”. Arbejdsrapport fra Miljøstyrelsen Nr. 38. Google Scholar


H Madadi , A Enkegaard , HF Brødsgaard , A Kharrazi-Pakdel , J Mohaghegh , A Ashouri . 2007. Host plant effects on the functional response of Neoseiulus cucumeris to onion thrips larvae. Journal of Applied Entomology 131(9–10): 728–733. Google Scholar


AF Montoya-Alvarez , K Ito , K Nakahira , R Arakawa. 2009. Functional response of Chrysoperla nipponensis and C. carnea (Neuroptera: Chrysopidae) to the cotton aphid Aphis gossypii Glover (Homoptera: Aphididae) under laboratory conditions. Applied Entomology and Zoology 45(1): 201–206. Google Scholar


JG Morse , BA Croft. 1987. Biological control of Aphispomi (Hom.; Aphididae) of Aphidoletes aphidimyza (Dip.: Cecidomyiidae): a predator-prey model. Entomophaga 32(4): 339–356. Google Scholar


G Mölck , U Wyss . 2003. Effect of aphidinfested plants on the host location and learning behaviour of the parasitoid Aphelinus abdominalis. Communications in Agricultural and Applied Biological Sciences 68(4a): 167–177. Google Scholar


G Mölck , SG Micha , U Wyss. 1999. Attraction to odour of infested plants and learning behaviour in the aphid parasitoid Aphelinus abdominalis. Zeitschrift für Pflanzenkrankheiten und Pflanzenschutz 106(6): 557–567. Google Scholar


SF Nielsen. 2006. Driftsanalyse af danske jordbaer 2004. Planteavlsorientering 6: 718. Google Scholar


BD Petersen , DH Christensen , OH Scharff. 2008. Jordbærnyt. Jordbœrnyt 5: 4. Google Scholar


JM Rabasse , C Trouve , A Geria , A Quignou . 2001. Aphid pests of strawberry crops and their parasitoids in France. Mededelingen Faculteit Landbouwkundige en Toegepaste Biologische Wetenschappen Universiteit Gent 66(2A): 293–301. Google Scholar


B Raymond , AC Darby , AE Douglas. 2000. The olfactory responses of coccinellids to aphids on plants. Entomologia Experimentalis et Applicata 95(1): 113–117. Google Scholar


SAS Institute Inc. 2008. SAS/STAT® 9.2 User's Guide. SAS Institute Inc. Google Scholar


R Sequeira , M Mackauer. 1994. Variation in selected life-history parameters of the parasitoid wasp, Aphidius ervi - influence of host developmental stage. Entomologia Experimentalis et Applicata 71(1): 15–22. Google Scholar


MA Shah. 1982. The influence of plant surfaces on the searching behaviour of Coccinellid larvae. Entomologia Experimentalis et Applicata 31(4): 377–380. Google Scholar


R Souissi , JP Nenon , Ru B Le. 1998. Olfactory responses of parasitoid Apoanagyrus lopezi to odor of plants, mealybugs, and plantmealybug complexes. Journal of Chemical Ecology 24(1): 37–48. Google Scholar


P Stary. 1988. Natural Enemies. In: AK Minks , P Harrewijn , Editors. Aphids, their Biology, Natural Enemies and Control. pp. 171–184. Elsevier. Google Scholar


H Takada , E Tada. 2000. A comparison between two strains from Japan and Europe of Aphidius ervi. Entomologia Experimentalis et Applicata 97(1): 11–20. Google Scholar


JE Timms , TH Oliver , NA Straw , SR Leather. 2008. The effects of host plant on the coccinellid functional response: Is the conifer specialist Aphidecta obliterata (L.) (Coleoptera: Coccinellidae) better adapted to spruce than the generalist Adalia bipunctata (L.) (Coleoptera: Coccinellidae)? Biological Control 47(3): 273–281. Google Scholar


MJ van Steenis. 1995. Evaluation of four aphidiine parasitoids for biological control of Aphis gossypii. Entomologia Experimentalis et Applicata 75(2): 151–157. Google Scholar


M Venzon , A Janssen , MW Sabelis. 1999. Attraction of a generalist predator towards herbivore-infested plants. Entomologia Experimentalis et Applicata 93(3): 305–314. Google Scholar


W Wahab. 1985. Observations on the biology and behaviour of Aphelinus abdominalis Dalm. (Hym., Aphelinidae), a parasite of aphids. Zeitschrift für Angewandte Entomologie 100(3): 290–296. Google Scholar


W Wahab , R Askew. 1989. Effect of temperature on the biology of Aphelinus abdominalis Dalman (Hymenoptera: Aphelinidae) a parasite of aphids. Bulletin of the Iraq Natural History Museum 8(2): 1–14. Google Scholar


RL Ware , B Yguel , MEN Majerus. 2008. Effects of larval diet on female reproductive output of the European coccinellid Adalia bipunctata and the invasive species Harmonia axyridis (Coleoptera: Coccinellidae). European Journal of Entomology 105(3): 437–443. Google Scholar


ENI Weeks , JG Logan , SA Gezan , CM Woodcock , MA Birkett , JA Pickett , MM Cameron. 2011. A bioassay for studying behavioural responses of the common bed bug, Cimex lectularis (Hemiptera: Cimcidae) to bed bugderived volatiles. Bulletin of Entomological Research 101(1): 1–8. Google Scholar


AA Zamani , A Talebi , Y Fathipour , C Baniameri. 2007. Effect of temperature on life history of Aphidius colemani and Aphidius matricariae (Hymenoptera: Braconidae), two parasitoids of Aphis gossypii and Myzus persicae (Homoptera: Aphididae. Environmental Entomology 36(2): 263–271. Google Scholar
This is an open access paper. We use the Creative Commons Attribution 3.0 license that permits unrestricted use, provided that the paper is properly attributed.
Annie Enkegaard, Lene Sigsgaard, and Kristian Kristensen "Shallot Aphids, Myzus ascalonicus, in Strawberry: Biocontrol Potential of Three Predators and Three Parasitoids," Journal of Insect Science 13(83), 1-16, (1 September 2013).
Received: 12 February 2012; Accepted: 1 August 2012; Published: 1 September 2013
Adalia bipunctata
Aphelinus abdominalis
Aphidius colemani
Aphidius ervi
Aphidoletes aphidimyza
Chrysoperla carnea
Back to Top