Diaeretiella rapae–parasitoid wasp of aphids

Biocontrol Agent Factsheet

Diaeretiella rapae is a species of parasitoid wasp that targets a wide variety of aphid pests.

Common Names

D. rapae

Relative effectiveness

D. rapae may be able to control low aphid populations but does not routinely provide adequate control of aphid pests on its own. Younger aphids that are parasitized by D. rapae usually do not reproduce before dying; older aphids will continue to mature and reproduce after being parasitized, although they will produce fewer offspring than unparasitized aphids. Taking measures to protect natural enemies of aphid pests, including D. rapae (see Conservation section, below), is an important part of an Integrated Pest Management approach to controlling aphids, but likely needs to be combined with other pest control practices to control heavy infestations.

Where to use

Many ornamental and food crops grown in agricultural fields and gardens

Outside

D. rapae parasitizes over 60 species of aphid pests of a wide range of cultivated plants. Some of the most economically important hosts of D. rapae are the cabbage aphid, Russian wheat aphid, and green peach aphid. Cabbage aphids attack plants in the brassica family, including cabbage, broccoli, cauliflower, Brussels sprouts, mustards, and radishes. Russian wheat aphid attacks grasses and cereal grains, primarily wheat, barley, rye, and triticale. Green peach aphids attack plants in over 40 families, including fruit trees in the family Prunus (e.g. apple, peach, apricot, plum) and most vegetable and ornamental crops.

About Diaeretiella rapae

Diaeretiella rapae is a small wasp that parasitizes more than 60 aphid species, including cabbage aphid, green peach aphid, and Russian wheat aphid. Females lay their eggs within living aphids. The resulting immature wasp (called a larva) consumes the aphid from within, killing it and creating a bronze-colored, dome-shaped aphid mummy. The wasp larva develops within the mummy and emerges as a new adult. D. rapae is widespread across the globe and occurs naturally across North America (compared to other parasitic wasps that must be intentionally released and do not persist in the environment). D. rapae does not usually provide sufficient control of aphid pests on its own.

  • Native/Non-native: Non-Native
  • Region: Throughout the United States
  • Established: Yes
  • Where established: Throughout the United States

Diaeretiella rapae Appearance

D. rapae is a small, dark wasp, about 2 mm long, with a skinny waist, a long, thin abdomen (rear-most section of the insect body), and long antennae. Because it is so small, it is difficult to find in the field, but may be seen on leaves infested with aphids, searching for hosts in which to lay eggs. When stinging aphid hosts, D. rapae quickly tucks its abdomen towards its head to pierce the host, which is usually situated close to the wasp’s head.

A small black wasp standing on a leaf, with its abdomen curved towards its head. Several aphids are also on the leaf.

Diaeretiella rapae in a stinging position.

Numerous cabbage aphids in a cluster, interspersed with several rounded, bronze-colored aphid mummies

A cabbage aphid colony with several rounded, bronze-colored aphid mummies, resulting from parasitism by D. rapae.

Diaeretiella rapae is a solitary endoparasite of aphids. Although females lay multiple eggs within each aphid host, only one larva lives to maturity. Females emerge from aphid hosts with fully developed eggs, and can lay fertilized or unfertilized eggs within new hosts (Kant et al. 2008). One study found that D. rapae females fed with buckwheat nectar had significantly higher egg loads than those fed on nectar from other flower species or water alone (Araj & Wratten 2015). New females will develop from fertilized eggs and males from unfertilized eggs, as is common with Hymenoptera (Kant et al. 2012a). 

Nectar is the primary food source for adult D. rapae. Other parasitoid species often feed on honeydew in addition to or instead of nectar, but cabbage aphid honeydew is coated in wax, making it inaccessible to D. rapae as a food source (Jamont et al. 2014). Without a nectar source, adults can survive for up to a few days, but access to nectar increases D. rapae longevity, fecundity, and host searching time (Varennes et al. 2015).

Females are attracted to host plants by volatiles given off by plants in the brassica family, and then find aphid hosts by searching randomly on the plant (Ayal 1987, Read et al. 2012). Males are attracted to host plants by an odor given off by female D. rapae (Reed et al. 2012). Research has found that D. rapae are more successful at finding larger (and therefore older) cabbage aphids than smaller/younger aphids, and prefer ovipositing into larger/older nymphs despite the older hosts having better defenses and requiring more handling time (Kant et al. 2012a). D. rapae preferentially lay eggs in host abdomens (Kant et al. 2008). A single female can produce up to several hundred offspring. The size of the host that a female emerges from has been shown to impact the number of offspring that female will produce, with females that developed from larger hosts producing 62% more offspring than those that developed in smaller hosts (Kant et al. 2012a).

D. rapae is a koinobiont species, meaning that their aphid hosts may continue to develop and reproduce even after being parasitized. However, if D. rapae parasitizes an aphid when the host is still small enough, the host may not contain enough resources for the developing wasp. The developing wasp may, in that case, consume aphid nymphs that are also developing within the host and the host may not produce any nymphs before being killed (Kant et al. 2012b). The D. rapae larva kills the aphid host within 2-3 days, leaving only a bronze-colored, hard aphid exoskeleton, now called a mummy. The developing wasp then pupates within the aphid mummy before emerging as a new adult. In a lab study, the entire life cycle from egg to adult took 9-15 days. Adult females live 10-15 days, males 7-10 days (Baer et al. 2004).

In temperate climates, D. rapae overwinters within aphid mummies on host plants (Geiger et al. 2005). Adults emerge in the spring to find aphid hosts.

How to Use Diaeretiella rapae

Biocontrol category: Conservation - attract and protect from the surrounding environment

Pest stage: Nymphs and Adults

Mode of action: Diaeretiella rapae is a parasitoid of aphid pests.

Conservation: Use targeted insecticides before turning to broad-spectrum insecticides to preserve natural enemies, including D. rapae. Adult D. rapae feed on nectar. Perennial flowering beds and/or annual insectary plantings can provide this nectar food source as well as habitat.

Compatibility: D. rapae can be killed by contact pesticides, if it is present in the crop when the pesticide is applied. Targeted pesticides, including flonicamid (e.g. Beleaf), pymetrozine (e.g. Fulfill), and sulfoxaflor (e.g. Closer, Transform) may not have an effect on D. rapae and can successfully control aphids. (Any time you use a pesticide, you must read and follow the label directions and comply with all applicable laws and regulations related to pesticide use. Also be sure that any pesticide used is approved for use in your country and state/province. )

Commercially available: No

Learn More

The historical range of D. rapae is Europe, the Mediterranean region, the Middle East, and Asia, although now it is found worldwide (Baer et al. 2004). D. rapae was introduced intentionally into some countries (e.g. Australia) and accidentally into other countries (e.g. New Zealand) (Kant et al. 2012). 

D. rapae was deliberately released into central and western U.S. between 1987 and 1994, as part of an attempt to control Russian wheat aphid (Diuraphis noxia), which can cause significant loss of grain crops and was first detected in the U.S. in 1986 (Noma et al. 2004, Tanigoshi et al. 1995). However, D. rapae had previously been reported throughout the U.S. before the releases in the 80s and 90s (Noma et al. 2004).

While D. rapae cannot usually control high aphid populations alone, conserving natural enemies of aphid pests, including D. rapae, is an important part of an Integrated Pest Management approach to controlling aphids. Practices for conserving D. rapae can fall into two categories: 1) increasing habitat and food sources for D. rapae adults and 2) avoiding insecticide applications that will reduce D. rapae populations.

D. rapae adults feed on nectar from flowering plants. While adults can survive and parasitize aphids without eating, feeding on nectar has been shown to increase the longevity, fecundity, and host searching time of D. rapae adults (Varennes et al. 2015). D. rapae are limited in what flowers they can obtain nectar from because they have short mouthparts they require flowers with open architecture or plants that produce extrafloral nectaries. Often, sufficient nectar is not available within crop plantings where aphid hosts are present, so adult D. rapae must split their time between feeding, traveling between nectar sources and host habitat, and searching for suitable hosts (Jamont et al. 2013). Insectary plantings can be included within or nearby crops that are susceptible to aphid pests, in order to provide habitat and nectar for D. rapae adults. A trial conducted in France showed that planting Vicia faba, a plant in the pea family that produces extrafloral nectaries, both attracted and retained D. rapae adults (Jamont et al. 2014). Limited work has been done to determine the preferred nectar source of D. rapae. One trial conducted in Jordan found that D. rapae adults that fed on nectar from buckwheat (Fagopyrum esculentum), white rocket (Diplotaxis erucoides), alyssum (Lobularia maritima), and shepherd’s purse (Capsella bursa-pastoris) all had increased longevity, egg load, and fecundity compared to the control (fed on water only), and buckwheat had a significantly greater effect that the other flower species (Araj & Wratten 2015). In trials conducted by the University of Massachusetts Extension Vegetable Program where insectary plantings were planted alongside Brussels sprouts, D. rapae was collected in greatest numbers from Ammi majus, compared to cilantro (Coriander sativum), dill (Anethum graveolens), alyssum, calendula (Calendula officinalis), and buckwheat (unpublished).

Aphids targeted by Diaeretiella rapae

  • Cabbage aphid (Brevicoryne brassicae)
  • Green peach aphid (Myzus persicae)
  • Russian wheat aphid (Diuraphis noxia)
  • Other aphid species (Aphidae) 

Aphids are small insects (1-3 mm long), with long antennae and legs and two additional appendages that stick out from the rear like stovepipes, called cornicles. Aphids are visible to the naked eye but it can be difficult to identify aphid species without a magnifying glass or microscope. Aphids can be various colors (green, gray, pink), depending on the species, and some species can vary in color widely. Aphid colonies usually consist of full-grown adults and various stages of immature aphids, called nymphs. Females can produce nymphs without mating. The resulting nymphs are genetically identical to the female parent and each other. Aphid nymphs are wingless, while adults can be wingless or winged. Winged adults look similar to a fruit fly.

Aphid Damage

Aphids cause crop damage by feeding on plant saps. Feeding can reduce yields, and if plants are heavily infested, the physical presence of the aphids on marketable parts of the plant can render crops unmarketable. Aphids also excrete a sugary substance called honeydew. Fungal growth called sooty mold can develop on the honeydew. Sooty mold is caused by several different fungi; while these fungi do not harm crops directly, sooty mold on crop surfaces can also render the crops unmarketable. Aphids generally prefer feeding in new growth.

Cabbage aphids feed on crops in the brassica family, and are particularly damaging to Brussels sprouts when they infest the buds. Feeding damage includes yellowing, wilting, distortion, and stunting. Cabbage aphids can also transmit plant viruses that can reduce crop yields.

Green peach aphids feed on a wide range of fruit, vegetable, greenhouse crops, landscape plants, and weeds. In addition to the feeding and infestation damage that green peach aphids can cause, they can also vector many plant viruses.

Russian wheat aphids feed on grasses and cereal grains, and are most damaging on wheat and barley, followed by rye and triticale. Toxins injected into the plant during feeding cause white, yellow, or purple longitudinal streaking on leaves. Infested leaves curl up longitudinally, like a drinking straw, and stand up rigidly instead of drooping over. The tip of the seed head can become stuck in the top-most leaf, causing the seedhead to form a fishhook-like shape.

Numerous gray-green cabbage aphids clustered in a group on the underside of a Brussels sprouts leaf.

Cabbage aphid (Brevicoryne brassicae) colony on the underside of a Brussels sprouts leaf.

Many green to pink aphids on the underside of a leaf.

Green peach aphid, adults and nymphs.Photo credit: Whitney Cranshaw, Colorado State University, Bugwood.org

Two yellow circles indicate irregularly shaped yellowing areas on the top side of a brassica leaf.

Yellowing visible on the top of a brassica leaf. Cabbage aphid colonies are present on the undersides of the yellow areas.

Many spindle-shaped, light-green aphids on a grass leaf. The leaf is white and green striped.

Russian wheat aphid colony, and white longitudinal stripes caused by aphid feeding.

One normal upright wheat seedhead and one wheat seedhead that is curled over, the tip stuck within the flagleaf.

Damage to wheat seedheads caused by Russian wheat aphid. Damaged seedhead on bottom. Awns are trapped in the damaged seedheads.

A green pepper fruit covered in dark-gray mold.

Sooty mold growing on aphid honeydew covering a pepper fruit.

D. rapae has been reported parasitizing over 60 species of aphids worldwide. It is perhaps the most well-known for parasitizing the cabbage aphid (Brevicoryne brassicae). Researchers in the Czech Republic found cabbage aphids to be the population diversity center for D. rapae, meaning that the population of D. rapae found attacking cabbage aphids was the most diverse of the populations found attacking a given host. D. rapae is also the most significant parasitoid of cabbage aphids. Researchers in Washington state found that 92.5% of parasitized aphids they collected were parasitized by D. rapae (Pike et al. 1999).

Cabbage aphid is a pest of brassica crops, including cabbage, broccoli, cauliflower, Brussels sprouts, mustards, radishes, and turnips. They are light-green but adults often appear gray because of the dusty/waxy coating that covers their exoskeleton. Adults are 2-2.5 mm long. Cabbage aphids have characteristically short cornicles (appendages that extend backwards from the rear of the abdomen), which distinguishes them from most other aphid species. Cabbage aphid colonies form on the undersides of host leaves. They preferentially infest new growth and are often found in growing points and in Brussels sprout buds. Feeding damage can cause stunting and deformation of crops, but the primary form of damage is the physical presence of the aphids themselves on marketable crop parts. In warm climates, or during warm seasons, females give birth to live nymphs. These nymphs are produced asexually and are genetically identical to the mother. Cold temperatures or reduction in photoperiod trigger the production of male aphids. Mating occurs and females lay eggs, which overwinter on host plants.

Green peach aphid (Myzus persicae), Russian wheat aphid (Diuraphis noxia), and asparagus aphid (Brachycorynella asparagi) are also significant hosts for D. rapae in the U.S. Green peach aphid feeds on plants in more than 40 families, including tree fruits, vegetables, and ornamentals. They overwinter in the egg state on Prunus spp. and in the spring, nymphs feed on Prunus flowers. When populations become too large, winged green peach aphids move to summer hosts. Feeding damage can result in leaf curling and yellowing, but green peach aphids also transmit many plant viruses, which is an important form of damage.

Asparagus aphids attack only asparagus and feed in ferns. A toxin injected into the plants during feeding causes shortening of internodes, causing ferns to develop a bush-like/witches-broom-like formation. Heavy infestations deplete sugars and cause reduced root growth, which can kill plants over a few years. Asparagus aphids can also vector viruses, including asparagus viruses I and II and tobacco streak virus. Asparagus aphids are oval-shaped and green-to-gray, and covered in a waxy secretion. They do not have cornicles but have openings at the rear of the abdomen in their place (UMass Fact Sheet). Russian wheat aphid feeds on cereal grains primarily wheat and barley, followed by rye and triticale. Oats sustain little to no damage from Russian wheat aphid, and corn, sorghum, and rice are not hosts. Toxins injected into the plants during feeding cause white or purple longitudinal streaks on the foliage, and infested leaves curl up longitudinally like drinking straws. The awn can become trapped in the curled flag leaf, giving the seed head a fishhook-like appearance.

Author

Genevieve Higgins
University of Massachusetts Extension Vegetable Program

Date: December 2021

Susan Scheufele, University of Massachusetts Extension Vegetable Program

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  • Ayal, Y. 1987. The foraging strategy of Diaeretiella rapae. Journal of Animal Ecology 56 (3): 1057-1068. 
  • Baer, C.F., Tripp, D. W., Bjorksten, A., Antonlin, M.F. 2004. Phylogeography of a parasitoid wasp (Diaeretiella rapae): no evidence of host-associated lineages. Molecular Ecology 13: 1959-1869.
  • Cabbage Aphid - Brevicoryne Brassicae Linnaeus.  Edited by Elena Rhodes, Featured Creatures, University of Florida.
  • Green Peach Aphid Myzus persicae (Sulzer).  Edited by Rhodes, E., Featured Creatures, University of Florida.
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  • Jamont, M., Dubois-Pot, C., and Jaloux, B. 2014. Nectar provisioning close to host patches increases parasitoid recruitment, retention and host parasitism. Basic and Applied Ecology 15: 151-160.
  • Jamont, M., Crépellière, S., and Jaloux, B. 2013. Effect of extrafloral nectar provisioning on the performance of the adult parasitoid Diaeretiella rapae. Biological Control 65: 271-277.
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  • Kant, R., Minor, M.A., Trewick, S. A., and Sandanayaka, W.R.M. 2012b. Body size and fitness relation in male and female Diaeretiella rapae. Biocontrol 57: 759-766.
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  • Pike, K.S., Stary, P., Miller, T., Allison, D., Graf, G., Bodyston, L., Miller, R., and Gillespie, R. 1999. Host range and habitats of the aphid parasitoid Diaeretiella rapae (Hymenoptera: Aphidiidae) in Washington state. Environmental Entomology 28 (1): 61-71.
  • Read, D., Feeny, P., and Root, R. 2012. Habitat selection by the aphid parasite Diaeretiella rapae (Hymenoptera: Braconidae) and hyperparasite Charips brassicae (Hymenoptera: Cynipidae). Canadian Entomologist 102(12): 1567-1578.
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  • Varennes, Y.-D., Gonzalez Chang, M., Boyer, S., and Wratten, S.D. 2016. Nectar feeding increases exploratory behavior in the aphid parasitoid Diaeretiella rapae (McIntosh). Journal of Applied Entomology 140: 479-483
  • A cabbage aphid colony with several rounded, bronze-colored aphid mummies, resulting from parasitism by D. rapae. Photo credit: UMass Extension Vegetable Program
    Diaeretiella rapae in a stinging position. Photo credit: Jack Kelly Clark, University of California Statewide IPM Program. Photo credit: Jack Kelly Clark, University of California Statewide IPM Program
  • Lifecycle of an aphid parasitoid. Photo credit: Natural Enemies of Vegetable Insect Pests, Hoffman & Frodsham 1993
  • Cabbage aphid (Brevicoryne brassicae) colony on the underside of a Brussels sprouts leaf. Photo credit: UMass Extension Vegetable Program
  • Russian wheat aphid colony, and white longitudinal stripes caused by aphid feeding. Photo credit: Phil Sloderbeck, Kansas State University, Bugwood.org
  • Damage to wheat seedheads caused by Russian wheat aphid. Awns are trapped in the seedheads. Photo credit: Frank Peairs, Colorado State University, Bugwood.org
  • Sooty mold growing on aphid honeydew covering a pepper fruit. Photo credit: Genevieve Higgins, UMass Extension Vegetable Program
Portrait of Amara Dunn
Amara Dunn-Silver

Biocontrol Specialist

Cornell Integrated Pest Management

Amara Dunn-Silver