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Parasitoid wasp

Parasitoid wasps are a large group of hymenopteran superfamilies, with all but the wood wasps (Orussoidea) being in the wasp-waisted Apocrita. As parasitoids, they lay their eggs on or in the bodies of other arthropods, sooner or later causing the death of these hosts. Different species specialise in hosts from different insect orders, most often Lepidoptera, though some select beetles, flies, or bugs; the spider wasps (Pompilidae) exclusively attack spiders.

Megarhyssa macrurus (Ichneumonidae), a parasitoid, ovipositing into its host through the wood of a tree. The body of a female is c. 2 inches (50 mm) long, with an ovipositor c. 4 inches (100 mm) long.
Females of the parasitoid wasp Neoneurus vesculus (Braconidae) ovipositing in workers of the ant Formica cunicularia.

Parasitoid wasp species differ in which host life-stage they attack: eggs, larvae, pupae, or adults. They mainly follow one of two major strategies within parasitism: either they are endoparasitic, developing inside the host, and koinobiont, allowing the host to continue to feed, develop, and moult; or they are ectoparasitic, developing outside the host, and idiobiont, paralysing the host immediately. Some endoparasitic wasps of the superfamily Ichneumonoidea have a mutualistic relationship with polydnaviruses, the viruses suppressing the host's immune defenses.[1]

Parasitoidism evolved only once in the Hymenoptera, during the Permian, leading to a single clade called Euhymenoptera,[2] but the parasitic lifestyle has secondarily been lost several times including among the ants, bees, and vespid wasps. As a result, the order Hymenoptera contains many families of parasitoids, intermixed with non-parasitoid groups. The parasitoid wasps include some very large groups, some estimates giving the Chalcidoidea as many as 500,000 species, the Ichneumonidae 100,000 species, and the Braconidae up to 50,000 species. Host insects have evolved a range of defences against parasitoid wasps, including hiding, wriggling, and camouflage markings.

Many parasitoid wasps are considered beneficial to humans because they naturally control agricultural pests. Some are applied commercially in biological pest control, starting in the 1920s with Encarsia formosa to control whitefly in greenhouses. Historically, parasitoidism in wasps influenced the thinking of Charles Darwin.[3]

Parasitoidism edit

 
Two strategies found among parasitoidal wasps: Ectoparasites are usually idiobiont, endoparasites koinobiont.

Parasitoid wasps range from some of the smallest species of insects to wasps about an inch long. Most females have a long, sharp ovipositor at the tip of the abdomen, sometimes lacking venom glands, and almost never modified into a sting.[4]

Parasitoids can be classified in a variety of ways. They can live within their host's body as endoparasitoids, or feed on it from outside as ectoparasitoids: both strategies are found among the wasps. Parasitoids can also be divided according to their effect on their hosts. Idiobionts prevent further development of the host after initially immobilizing it, while koinobionts allow the host to continue its development while they are feeding upon it; and again, both types are seen in parasitoidal wasps. Most ectoparasitoid wasps are idiobiont, as the host could damage or dislodge the external parasitoid if allowed to move or moult. Most endoparasitoid wasps are koinobionts, giving them the advantage of a host that continues to grow larger and remains able to avoid predators.[4]

 
Spider wasp (Pompilidae), an idiobiont, carrying a jumping spider she has just paralysed back to her nest, where she will lay an egg on it.

Hosts edit

Many parasitoid wasps use larval Lepidoptera as hosts, but some groups parasitize different host life stages (egg, larva or nymph, pupa, adult) of nearly all other orders of insects, especially Coleoptera, Diptera, Hemiptera and other Hymenoptera. Some attack arthropods other than insects: for instance, the Pompilidae specialise in catching spiders: these are quick and dangerous prey, often as large as the wasp itself, but the spider wasp is quicker, swiftly stinging her prey to immobilise it. Adult female wasps of most species oviposit into their hosts' bodies or eggs. More rarely, parasitoid wasps may use plant seeds as hosts, such as Torymus druparum.[5]

Some also inject a mix of secretory products that paralyse the host or protect the egg from the host's immune system; these include polydnaviruses, ovarian proteins, and venom. If a polydnavirus is included, it infects the nuclei of host hemocytes and other cells, causing symptoms that benefit the parasite.[6][7]

 
An apparently healthy moth caterpillar feeds, grows, and molts...
 
...but endoparasitic koinobiont wasp larvae eventually fill its body and kill it.

Host size is important for the development of the parasitoid, as the host is its entire food supply until it emerges as an adult; small hosts often produce smaller parasitoids.[8] Some species preferentially lay female eggs in larger hosts and male eggs in smaller hosts, as the reproductive capabilities of males are limited less severely by smaller adult body size.[9]

 
Hornworm with parasitic wasp cocoons

Some parasitoid wasps mark the host with chemical signals to show that an egg has been laid there. This may both deter rivals from ovipositing, and signal to itself that no further egg is needed in that host, effectively reducing the chances that offspring will have to compete for food and increasing the offspring's survival.[10][11]

Life cycle edit

 
Potter wasp (Eumeninae), an idiobiont, building mud nest; she will then provision it with paralysed insects, on which she lays her eggs; she then seals the nest and provides no further care for her young.

On or inside the host the parasitoid egg hatches into a larva or two or more larvae (polyembryony). Endoparasitoid eggs can absorb fluids from the host body and grow several times in size from when they were first laid before hatching. The first instar larvae are often highly mobile and may have strong mandibles or other structures to compete with other parasitoid larvae. The following instars are generally more grub-like. Parasitoid larvae have incomplete digestive systems with no rear opening. This prevents the hosts from being contaminated by their wastes. The larva feeds on the host's tissues until ready to pupate; by then the host is generally either dead or almost so. A meconium, or the accumulated wastes from the larva is cast out as the larva transitions to a prepupa.[12][13] Depending on its species, the parasitoid then may eat its way out of the host or remain in the more or less empty skin. In either case it then generally spins a cocoon and pupates. As adults, parasitoid wasps feed primarily on nectar from flowers. Females of some species will also drink hemolymph from hosts to gain additional nutrients for egg production.[14]

 
Polydnavirus-wasp mutualism: the virus protects koinobiont wasp eggs and larvae from immune suppression by the host's hemocytes.

Mutualism with polydnavirus edit

Polydnaviruses are a unique group of insect viruses that have a mutualistic relationship with some parasitic wasps. The polydnavirus replicates in the oviducts of an adult female parasitoid wasp. The wasp benefits from this relationship because the virus provides protection for the parasitic larvae inside the host, (i) by weakening the host's immune system and (ii) by altering the host's cells to be more beneficial to the parasite. The relationship between these viruses and the wasp is obligatory in the sense that all individuals are infected with the viruses; the virus has been incorporated in the wasp's genome and is inherited.[15][16][17]

Host defenses edit

 
Parasitoid wasp (Ichneumonidae) pointing ovipositor at cinnabar moth larva, just after ovipositing. The larva wriggles vigorously to try to avoid the attack.

The hosts of parasitoids have developed several levels of defence. Many hosts try to hide from the parasitoids in inaccessible habitats. They may also get rid of their frass (body wastes) and avoid plants that they have chewed on as both can signal their presence to parasitoids hunting for hosts. The egg shells and cuticles of the potential hosts are thickened to prevent the parasitoid from penetrating them. Hosts may use behavioral evasion when they encounter an egg laying female parasitoid, like dropping off the plant they are on, twisting and thrashing so as to dislodge or kill the female and even regurgitating onto the wasp to entangle it. The wriggling can sometimes help by causing the wasp to "miss" laying the egg on the host and instead place it nearby. Wriggling of pupae can cause the wasp to lose its grip on the smooth hard pupa or get trapped in the silk strands. Some caterpillars even bite the female wasps that approach them. Some insects secrete poisonous compounds that kill or drive away the parasitoid. Ants that are in a symbiotic relationship with caterpillars, aphids or scale insects may protect them from attack by wasps.[18][19]

Parasitoid wasps are vulnerable to hyperparasitoid wasps. Some parasitoid wasps change the behavior of the infected host, causing them to build a silk web around the pupae of the wasps after they emerge from its body to protect them from hyperparasitoids.[20]

Hosts can kill endoparasitoids by sticking haemocytes to the egg or larva in a process called encapsulation.[21] In aphids, the presence of a particular species of γ-3 Pseudomonadota makes the aphid relatively immune to their parasitoid wasps by killing many of the eggs. As the parasitoid's survival depends on its ability to evade the host's immune response, some parasitoid wasps have developed the counterstrategy of laying more eggs in aphids that have the endosymbiont, so that at least one of them may hatch and parasitize the aphid.[22][23]

Certain caterpillars eat plants that are toxic to both themselves and the parasite to cure themselves.[24] Drosophila melanogaster larvae also self-medicate with ethanol to treat parasitism.[25] D. melanogaster females lay their eggs in food containing toxic amounts of alcohol if they detect parasitoid wasps nearby. The alcohol protects them from the wasps, at the cost of retarding their own growth.[26]

Evolution and taxonomy edit

Evolution edit

Based on genetic and fossil analysis, parasitoidism has evolved only once in the Hymenoptera, during the Permian, leading to a single clade. All parasitoid wasps are descended from this lineage. The narrow-wasted Apocrita emerged during the Jurassic. [27][28][29][30] The Aculeata, which includes bees, ants, and parasitoid spider wasps, evolved from within the Apocrita; it contains many families of parasitoids, though not the Ichneumonoidea, Cynipoidea, and Chalcidoidea. The Hymenoptera, Apocrita, and Aculeata are all clades, but since each of these contains non-parasitic species, the parasitoid wasps, formerly known as the Parasitica, do not form a clade on their own.[30][31] The common ancestor in which parasitoidism evolved lived approximately 247 million years ago and was previously believed to be an ectoparasitoid wood wasp that fed on wood-boring beetle larvae. Species similar in lifestyle and morphology to this ancestor still exist in the Ichneumonoidea.[32][33] However, recent molecular and morphological analysis suggests this ancestor was endophagous, meaning it fed from within its host.[30] A significant radiation of species in the Hymenoptera occurred shortly after the evolution of parasitoidy in the order and is thought to have been a result of it.[31][33] The evolution of a wasp waist, a constriction in the abdomen of the Apocrita, contributed to rapid diversification as it increased maneuverability of the ovipositor, the organ off the rear segment of the abdomen used to lay eggs.[34]

The phylogenetic tree gives a condensed overview of the positions of parasitoidal groups (boldface), amongst groups (italics) like the Vespidae which have secondarily abandoned the parasitoid habit. The approximate numbers of species estimated to be in these groups, often much larger than the number so far described, is shown in parentheses, with estimates for the most populous also shown in boldface, like "(150,000)". Not all species in these groups are parasitoidal: for example, some Cynipoidea are phytophagous.

Hymenoptera

Sawflies  

parasitoidism

Orussoidea (parasitoid wood wasps, 85)  

Apocrita

Ichneumonoidea (150,000)  

Cynipoidea (3,000)  

Proctotrupoidea (400)  

Platygastroidea (4000)  

Chalcidoidea (500,000)  

other Superfamilies

Aculeata

Chrysididae (jewel wasps, 3000)  

Vespidae (wasps, hornets, 5000)  

Mutillidae (velvet ants, 3000)  

Pompilidae (spider wasps, 5000)  

other families

Scoliidae (560)  

Formicidae (ants, 22,000)  

Apoidea

Sphecidae (700)  

Bembicinae (1800)  

other families

Pemphredoninae (aphid wasps, 1000)  

Philanthinae (1100)  

Anthophila (bees, 22,000)  

stinging
wasp waist
evolved once

Taxonomy edit

 
Trissolcus (family Platygastridae) on Chinavia eggs
 
Housefly pupae killed by parasitoid wasp larvae (probably Pteromalidae). Each pupa has one hole through which a single adult wasp has emerged after feeding on the housefly larva.

The parasitoid wasps are paraphyletic since the ants, bees, and non-parasitic wasps such as the Vespidae are not included, and there are many members of mainly parasitoidal families which are not themselves parasitic. Listed are Hymenopteran families where most members have a parasitoid lifestyle.[35]

Interactions with humans edit

Biological pest control edit

 
Encarsia formosa, an endoparasitic aphelinid wasp, bred commercially to control whitefly in greenhouses
 
Trioxys complanatus, (Aphidiinae) ovipositing into a spotted alfalfa aphid, a commercial pest in Australia.[a]

Parasitoid wasps are considered beneficial as they naturally control the population of many pest insects. They are widely used commercially (alongside other parasitoids such as tachinid flies) for biological pest control, for which the most important groups are the ichneumonid wasps, which prey mainly on caterpillars of butterflies and moths; braconid wasps, which attack caterpillars and a wide range of other insects including greenfly; chalcidoid wasps, which parasitise eggs and larvae of greenfly, whitefly, cabbage caterpillars, and scale insects.[37]

One of the first parasitoid wasps to enter commercial use was Encarsia formosa, an endoparasitic aphelinid. It has been used to control whitefly in greenhouses since the 1920s. Use of the insect fell almost to nothing, replaced by chemical pesticides by the 1940s. Since the 1970s, usage has revived, with renewed usage in Europe and Russia.[38] In some countries, such as New Zealand, it is the primary biological control agent used to control greenhouse whiteflies, particularly on crops such as tomato, a particularly difficult plant for predators to establish on.[39]

Commercially, there are two types of rearing systems: short-term seasonal daily output with high production of parasitoids per day, and long-term year-round low daily output with a range in production of 4–1000 million female parasitoids per week, to meet demand for suitable parasitoids for different crops.[40]

In culture edit

Parasitoid wasps influenced the thinking of Charles Darwin.[b] In an 1860 letter to the American naturalist Asa Gray, Darwin wrote: "I cannot persuade myself that a beneficent and omnipotent God would have designedly created parasitic wasps with the express intention of their feeding within the living bodies of Caterpillars."[3] The palaeontologist Donald Prothero notes that religiously-minded people of the Victorian era, including Darwin, were horrified by this instance of evident cruelty in nature, particularly noticeable in the Ichneumonidae.[42]

Notes edit

  1. ^ Trioxys complanatus has been introduced to Australia to control the spotted alfalfa aphid.[36]
  2. ^ Darwin mentions "parasitic" wasps in On the Origin of Species, Chapter 7, page 218.[41]

References edit

  1. ^ Herniou, Elisabeth A.; Huguet, Elisabeth; Thézé, Julien; Bézier, Annie; Periquet, Georges; Drezen, Jean-Michel (2013-09-19). "When parasitic wasps hijacked viruses: genomic and functional evolution of polydnaviruses". Phil. Trans. R. Soc. B. 368 (1626): 20130051. doi:10.1098/rstb.2013.0051. PMC 3758193. PMID 23938758.
  2. ^ Zhang, Qi; Kopylov, Dmitry S.; Rasnitsyn, Alexandr P.; Zheng, Yan; Zhang, Haichun (November 2020). Smith, Andrew (ed.). "Burmorussidae, a new family of parasitic wasps (Insecta, Hymenoptera) from mid‐Cretaceous Burmese amber". Papers in Palaeontology. 6 (4): 593–603. doi:10.1002/spp2.1312. ISSN 2056-2802. S2CID 219039881.
  3. ^ a b "Letter 2814 — Darwin, C. R. to Gray, Asa, 22 May [1860]". Retrieved 2011-04-05.
  4. ^ a b Gullan, P. J.; Cranston, P. S. (2010). The Insects: An Outline of Entomology (5th ed.). Wiley. pp. 362–370. ISBN 978-1-118-84615-5.
  5. ^ Cushman R. A. (1916). "Syntomaspis druparum, the apple-seed chalcid". Journal of Agricultural Research. 7: 487–502.
  6. ^ Miller, Lois K.; Ball, Laurence Andrew (1998). The insect viruses. Springer. ISBN 978-0-306-45881-1.
  7. ^ Strand, Michael R.; Burke, Gaelen R. (May 2015). "Polydnaviruses: From discovery to current insights". Virology. 479–480: 393–402. doi:10.1016/j.virol.2015.01.018. PMC 4424053. PMID 25670535.
  8. ^ Cohen, J. E.; Jonsson, T.; Muller, C. B.; Godfray, H. C. J.; Savage, V. M. (12 January 2005). "Body sizes of hosts and parasitoids in individual feeding relationships". Proceedings of the National Academy of Sciences. 102 (3): 684–689. Bibcode:2005PNAS..102..684C. doi:10.1073/pnas.0408780102. PMC 545575. PMID 15647346. 
  9. ^ Jones, W. Thomas (1982). "Sex Ratio and Host Size in a Parasitoid Wasp". Behavioral Ecology and Sociobiology. 10 (3): 207–210. doi:10.1007/bf00299686. JSTOR 4599484. S2CID 28101144.
  10. ^ Couchoux, Christelle; Seppä, Perttu; van Nouhuys, Saskya (2015). "Behavioural and genetic approaches to evaluate the effectiveness of deterrent marking by a parasitoid wasp". Behaviour. 152 (9): 1257–1276. doi:10.1163/1568539X-00003277.
  11. ^ Nufio, César R.; Papaj, Daniel R. (2001). "Host marking behavior in phytophagous insects and parasitoids". Entomologia Experimentalis et Applicata. 99 (3): 273–293. doi:10.1046/j.1570-7458.2001.00827.x. 
  12. ^ Paladino, Leonela Zusel Carabajal; Papeschi, Alba Graciela; Cladera, Jorge Luis (January 2010). "Immature stages of development in the parasitoid wasp, Diachasmimorpha longicaudata". Journal of Insect Science. 10 (1): 56. doi:10.1673/031.010.5601. PMC 3014816. PMID 20569133. 
  13. ^ "Cotesia congregata - a parasitoid wasp". entnemdept.ufl.edu. Retrieved 2017-10-02.
  14. ^ Jervis, M. A.; Kidd, N. A. C (November 1986). "Host-Feeding Strategies in Hymenopteran Parasitoids". Biological Reviews. 61 (4): 395–434. doi:10.1111/j.1469-185x.1986.tb00660.x. S2CID 84430254.
  15. ^ Fleming, J. G.; Summers, M. D. (1991). "Polydnavirus DNA is integrated in the DNA of its parasitoid wasp host". PNAS. 88 (21): 9770–9774. Bibcode:1991PNAS...88.9770F. doi:10.1073/pnas.88.21.9770. PMC 52802. PMID 1946402.
  16. ^ Webb, Bruce A. (1998). "Polydnavirus Biology, Genome Structure, and Evolution". In Miller, L.K.; Ball, L.A. (eds.). The Insect Viruses. Springer, Boston, MA. pp. 105–139. doi:10.1007/978-1-4615-5341-0_5. ISBN 9781461374374.
  17. ^ Roossinck, M. J. (2011). "Changes in population dynamics in mutualistic versus pathogenic viruses". Viruses. 3 (12): 12–19. doi:10.3390/v3010012. PMC 3187592. PMID 21994724. 
  18. ^ Strand, M. R.; Pech, L. L. (1995). "Immunological Basis for Compatibility in Parasitoid-Host Relationships". Annual Review of Entomology. 40: 31–56. doi:10.1146/annurev.en.40.010195.000335. PMID 7810989.
  19. ^ Gross, P. (1993). "Insect Behavioral and Morphological defences Against Parasitoids". Annual Review of Entomology. 38: 251–273. doi:10.1146/annurev.en.38.010193.001343.
  20. ^ Tanaka, S.; Ohsaki, N. (2006). "Behavioral manipulation of host caterpillars by the primary parasitoid wasp Cotesia glomerata (L.) to construct defensive webs against hyperparasitism". Ecological Research. 21 (4): 570. doi:10.1007/s11284-006-0153-2. S2CID 23457678.
  21. ^ Pennacchio, Francesco; Caccia, Silvia; Digilio, Maria Cristina (December 2014). "Host regulation and nutritional exploitation by parasitic wasps". Current Opinion in Insect Science. 6: 74–79. doi:10.1016/j.cois.2014.09.018. ISSN 2214-5745. PMID 32846685.
  22. ^ Oliver, K. M.; Russell, J. A.; Moran, N. A.; Hunter, M. S. (2003). "Facultative bacterial symbionts in aphids confer resistance to parasitic wasps". Proceedings of the National Academy of Sciences. 100 (4): 1803–7. Bibcode:2003PNAS..100.1803O. doi:10.1073/pnas.0335320100. PMC 149914. PMID 12563031.
  23. ^ Oliver, K. M.; Noge, K.; Huang, E. M.; Campos, J. M.; Becerra, J. X.; Hunter, M. S. (2012). "Parasitic wasp responses to symbiont-based defence in aphids". BMC Biology. 10: 11. doi:10.1186/1741-7007-10-11. PMC 3312838. PMID 22364271.
  24. ^ Singer, M. S.; Mace, K. C.; Bernays, E. A. (2009). May, Robin Charles (ed.). "Self-Medication as Adaptive Plasticity: Increased Ingestion of Plant Toxins by Parasitized Caterpillars". PLOS ONE. 4 (3): e4796. Bibcode:2009PLoSO...4.4796S. doi:10.1371/journal.pone.0004796. PMC 2652102. PMID 19274098.
  25. ^ Milan, N. F.; Kacsoh, B. Z.; Schlenke, T. A. (2012). "Alcohol Consumption as Self-Medication against Blood-Borne Parasites in the Fruit Fly". Current Biology. 22 (6): 488–493. doi:10.1016/j.cub.2012.01.045. PMC 3311762. PMID 22342747.
  26. ^ Kacsoh, B. Z.; Lynch, Z. R.; Mortimer, N. T.; Schlenke, T. A. (2013). "Fruit Flies Medicate Offspring After Seeing Parasites". Science. 339 (6122): 947–50. Bibcode:2013Sci...339..947K. doi:10.1126/science.1229625. PMC 3760715. PMID 23430653.
  27. ^ Branstetter, Michael G.; Danforth, Bryan N.; Pitts, James P.; Faircloth, Brant C.; Ward, Philip S.; Buffington, Matthew L.; Gates, Michael W.; Kula, Robert R.; Brady, Seán G. (2017). "Phylogenomic Insights into the Evolution of Stinging Wasps and the Origins of Ants and Bees". Current Biology. 27 (7): 1019–1025. doi:10.1016/j.cub.2017.03.027. PMID 28376325. 
  28. ^ Schulmeister, S. (2003). "Simultaneous analysis of basal Hymenoptera (Insecta), introducing robust-choice sensitivity analysis". Biological Journal of the Linnean Society. 79 (2): 245–275. doi:10.1046/j.1095-8312.2003.00233.x. 
  29. ^ Schulmeister, S. "Symphyta". Retrieved 28 November 2016.
  30. ^ a b c Peters, Ralph S.; Krogmann, Lars; Mayer, Christoph; Donath, Alexander; Gunkel, Simon; Meusemann, Karen; Kozlov, Alexey; Podsiadlowski, Lars; Petersen, Malte (2017). "Evolutionary History of the Hymenoptera". Current Biology. 27 (7): 1013–1018. doi:10.1016/j.cub.2017.01.027. hdl:2434/801122. PMID 28343967.
  31. ^ a b Heraty, John; Ronquist, Fredrik; Carpenter, James M.; Hawks, David; Schulmeister, Susanne; Dowling, Ashley P.; Murray, Debra; Munro, James; Wheeler, Ward C. (2011). "Evolution of the hymenopteran megaradiation" (PDF). Molecular Phylogenetics and Evolution. 60 (1): 73–88. doi:10.1016/j.ympev.2011.04.003. PMID 21540117.
  32. ^ Pennacchio, Francesco; Strand, Michael R. (January 2006). "Evolution of developmental strategies in parasitic hymenoptera". Annual Review of Entomology. 51 (1): 233–258. doi:10.1146/annurev.ento.51.110104.151029. PMID 16332211.
  33. ^ a b Whitfield, James B. (2003). "Phylogenetic Insights into the Evolution of Parasitism in Hymenoptera". Advances in Parasitology. 54: 69–100. doi:10.1016/S0065-308X(03)54002-7. ISBN 978-0-12-031754-7. PMID 14711084.
  34. ^ Peters, Ralph S.; Krogmann, Lars; Mayer, Christoph; Donath, Alexander; Gunkel, Simon; Meusemann, Karen; Kozlov, Alexey; Podsiadlowski, Lars; Petersen, Malte (April 2017). "Evolutionary History of the Hymenoptera". Current Biology. 27 (7): 1013–1018. doi:10.1016/j.cub.2017.01.027. hdl:2434/801122. ISSN 0960-9822. PMID 28343967.
  35. ^ Henri, Goulet; Theodore), Huber, John T. (John; Branch, Canada. Agriculture Canada. Research (1993). Hymenoptera of the world : an identification guide to families. Centre for Land and Biological Resources Research. ISBN 978-0660149332. OCLC 28024976.{{cite book}}: CS1 maint: multiple names: authors list (link)
  36. ^ Wilson, C. G.; Swincer, D. E.; Walden, K. J. (1982). "The Introduction of Trioxys Complanatus Quilis (Hymenoptera: Aphidiidae), an Internal Parasite of the Spotted Alfalfa Aphid, into South Australia". Australian Journal of Entomology. 21 (1): 13–27. doi:10.1111/j.1440-6055.1982.tb01758.x.
  37. ^ "Parasitoid Wasps (Hymenoptera)". University of Maryland. Retrieved 6 June 2016.
  38. ^ Hoddle, M. S.; Van Driesche, R. G.; Sanderson, J. P. (1998). "Biology and Use of the Whitefly Parasitoid Encarsia Formosa". Annual Review of Entomology. 43 (1): 645–669. doi:10.1146/annurev.ento.43.1.645. PMID 15012401.
  39. ^ "Enforce for Greenhouse Whitefly Control". New Zealand: Bioforce Limited. Retrieved 26 January 2024.
  40. ^ Smith, S. M. (1996). "Biological control with Trichogramma: advances, successes, and potential of their use". Annual Review of Entomology. 41: 375–406. doi:10.1146/annurev.en.41.010196.002111. PMID 15012334.
  41. ^ On the Origin of Species, Chapter 7, page 218.
  42. ^ Prothero, Donald R. (2017). Evolution: What the Fossils Say and Why It Matters. Columbia University Press. pp. 84–86. ISBN 978-0-231-54316-3.

parasitoid, wasp, large, group, hymenopteran, superfamilies, with, wood, wasps, orussoidea, being, wasp, waisted, apocrita, parasitoids, they, their, eggs, bodies, other, arthropods, sooner, later, causing, death, these, hosts, different, species, specialise, . Parasitoid wasps are a large group of hymenopteran superfamilies with all but the wood wasps Orussoidea being in the wasp waisted Apocrita As parasitoids they lay their eggs on or in the bodies of other arthropods sooner or later causing the death of these hosts Different species specialise in hosts from different insect orders most often Lepidoptera though some select beetles flies or bugs the spider wasps Pompilidae exclusively attack spiders Megarhyssa macrurus Ichneumonidae a parasitoid ovipositing into its host through the wood of a tree The body of a female is c 2 inches 50 mm long with an ovipositor c 4 inches 100 mm long source source source source source Females of the parasitoid wasp Neoneurus vesculus Braconidae ovipositing in workers of the ant Formica cunicularia Parasitoid wasp species differ in which host life stage they attack eggs larvae pupae or adults They mainly follow one of two major strategies within parasitism either they are endoparasitic developing inside the host and koinobiont allowing the host to continue to feed develop and moult or they are ectoparasitic developing outside the host and idiobiont paralysing the host immediately Some endoparasitic wasps of the superfamily Ichneumonoidea have a mutualistic relationship with polydnaviruses the viruses suppressing the host s immune defenses 1 Parasitoidism evolved only once in the Hymenoptera during the Permian leading to a single clade called Euhymenoptera 2 but the parasitic lifestyle has secondarily been lost several times including among the ants bees and vespid wasps As a result the order Hymenoptera contains many families of parasitoids intermixed with non parasitoid groups The parasitoid wasps include some very large groups some estimates giving the Chalcidoidea as many as 500 000 species the Ichneumonidae 100 000 species and the Braconidae up to 50 000 species Host insects have evolved a range of defences against parasitoid wasps including hiding wriggling and camouflage markings Many parasitoid wasps are considered beneficial to humans because they naturally control agricultural pests Some are applied commercially in biological pest control starting in the 1920s with Encarsia formosa to control whitefly in greenhouses Historically parasitoidism in wasps influenced the thinking of Charles Darwin 3 Contents 1 Parasitoidism 1 1 Hosts 1 2 Life cycle 1 3 Mutualism with polydnavirus 2 Host defenses 3 Evolution and taxonomy 3 1 Evolution 3 2 Taxonomy 4 Interactions with humans 4 1 Biological pest control 4 2 In culture 5 Notes 6 ReferencesParasitoidism edit nbsp Two strategies found among parasitoidal wasps Ectoparasites are usually idiobiont endoparasites koinobiont Further information Parasitoid Parasitoid wasps range from some of the smallest species of insects to wasps about an inch long Most females have a long sharp ovipositor at the tip of the abdomen sometimes lacking venom glands and almost never modified into a sting 4 Parasitoids can be classified in a variety of ways They can live within their host s body as endoparasitoids or feed on it from outside as ectoparasitoids both strategies are found among the wasps Parasitoids can also be divided according to their effect on their hosts Idiobionts prevent further development of the host after initially immobilizing it while koinobionts allow the host to continue its development while they are feeding upon it and again both types are seen in parasitoidal wasps Most ectoparasitoid wasps are idiobiont as the host could damage or dislodge the external parasitoid if allowed to move or moult Most endoparasitoid wasps are koinobionts giving them the advantage of a host that continues to grow larger and remains able to avoid predators 4 nbsp Spider wasp Pompilidae an idiobiont carrying a jumping spider she has just paralysed back to her nest where she will lay an egg on it Hosts edit Many parasitoid wasps use larval Lepidoptera as hosts but some groups parasitize different host life stages egg larva or nymph pupa adult of nearly all other orders of insects especially Coleoptera Diptera Hemiptera and other Hymenoptera Some attack arthropods other than insects for instance the Pompilidae specialise in catching spiders these are quick and dangerous prey often as large as the wasp itself but the spider wasp is quicker swiftly stinging her prey to immobilise it Adult female wasps of most species oviposit into their hosts bodies or eggs More rarely parasitoid wasps may use plant seeds as hosts such as Torymus druparum 5 Some also inject a mix of secretory products that paralyse the host or protect the egg from the host s immune system these include polydnaviruses ovarian proteins and venom If a polydnavirus is included it infects the nuclei of host hemocytes and other cells causing symptoms that benefit the parasite 6 7 nbsp An apparently healthy moth caterpillar feeds grows and molts nbsp but endoparasitic koinobiont wasp larvae eventually fill its body and kill it Host size is important for the development of the parasitoid as the host is its entire food supply until it emerges as an adult small hosts often produce smaller parasitoids 8 Some species preferentially lay female eggs in larger hosts and male eggs in smaller hosts as the reproductive capabilities of males are limited less severely by smaller adult body size 9 nbsp Hornworm with parasitic wasp cocoonsSome parasitoid wasps mark the host with chemical signals to show that an egg has been laid there This may both deter rivals from ovipositing and signal to itself that no further egg is needed in that host effectively reducing the chances that offspring will have to compete for food and increasing the offspring s survival 10 11 Life cycle edit nbsp Potter wasp Eumeninae an idiobiont building mud nest she will then provision it with paralysed insects on which she lays her eggs she then seals the nest and provides no further care for her young On or inside the host the parasitoid egg hatches into a larva or two or more larvae polyembryony Endoparasitoid eggs can absorb fluids from the host body and grow several times in size from when they were first laid before hatching The first instar larvae are often highly mobile and may have strong mandibles or other structures to compete with other parasitoid larvae The following instars are generally more grub like Parasitoid larvae have incomplete digestive systems with no rear opening This prevents the hosts from being contaminated by their wastes The larva feeds on the host s tissues until ready to pupate by then the host is generally either dead or almost so A meconium or the accumulated wastes from the larva is cast out as the larva transitions to a prepupa 12 13 Depending on its species the parasitoid then may eat its way out of the host or remain in the more or less empty skin In either case it then generally spins a cocoon and pupates As adults parasitoid wasps feed primarily on nectar from flowers Females of some species will also drink hemolymph from hosts to gain additional nutrients for egg production 14 nbsp Polydnavirus wasp mutualism the virus protects koinobiont wasp eggs and larvae from immune suppression by the host s hemocytes Mutualism with polydnavirus edit Main article Polydnavirus Polydnaviruses are a unique group of insect viruses that have a mutualistic relationship with some parasitic wasps The polydnavirus replicates in the oviducts of an adult female parasitoid wasp The wasp benefits from this relationship because the virus provides protection for the parasitic larvae inside the host i by weakening the host s immune system and ii by altering the host s cells to be more beneficial to the parasite The relationship between these viruses and the wasp is obligatory in the sense that all individuals are infected with the viruses the virus has been incorporated in the wasp s genome and is inherited 15 16 17 Host defenses edit nbsp Parasitoid wasp Ichneumonidae pointing ovipositor at cinnabar moth larva just after ovipositing The larva wriggles vigorously to try to avoid the attack The hosts of parasitoids have developed several levels of defence Many hosts try to hide from the parasitoids in inaccessible habitats They may also get rid of their frass body wastes and avoid plants that they have chewed on as both can signal their presence to parasitoids hunting for hosts The egg shells and cuticles of the potential hosts are thickened to prevent the parasitoid from penetrating them Hosts may use behavioral evasion when they encounter an egg laying female parasitoid like dropping off the plant they are on twisting and thrashing so as to dislodge or kill the female and even regurgitating onto the wasp to entangle it The wriggling can sometimes help by causing the wasp to miss laying the egg on the host and instead place it nearby Wriggling of pupae can cause the wasp to lose its grip on the smooth hard pupa or get trapped in the silk strands Some caterpillars even bite the female wasps that approach them Some insects secrete poisonous compounds that kill or drive away the parasitoid Ants that are in a symbiotic relationship with caterpillars aphids or scale insects may protect them from attack by wasps 18 19 Parasitoid wasps are vulnerable to hyperparasitoid wasps Some parasitoid wasps change the behavior of the infected host causing them to build a silk web around the pupae of the wasps after they emerge from its body to protect them from hyperparasitoids 20 Hosts can kill endoparasitoids by sticking haemocytes to the egg or larva in a process called encapsulation 21 In aphids the presence of a particular species of g 3 Pseudomonadota makes the aphid relatively immune to their parasitoid wasps by killing many of the eggs As the parasitoid s survival depends on its ability to evade the host s immune response some parasitoid wasps have developed the counterstrategy of laying more eggs in aphids that have the endosymbiont so that at least one of them may hatch and parasitize the aphid 22 23 Certain caterpillars eat plants that are toxic to both themselves and the parasite to cure themselves 24 Drosophila melanogaster larvae also self medicate with ethanol to treat parasitism 25 D melanogaster females lay their eggs in food containing toxic amounts of alcohol if they detect parasitoid wasps nearby The alcohol protects them from the wasps at the cost of retarding their own growth 26 Evolution and taxonomy editEvolution edit Based on genetic and fossil analysis parasitoidism has evolved only once in the Hymenoptera during the Permian leading to a single clade All parasitoid wasps are descended from this lineage The narrow wasted Apocrita emerged during the Jurassic 27 28 29 30 The Aculeata which includes bees ants and parasitoid spider wasps evolved from within the Apocrita it contains many families of parasitoids though not the Ichneumonoidea Cynipoidea and Chalcidoidea The Hymenoptera Apocrita and Aculeata are all clades but since each of these contains non parasitic species the parasitoid wasps formerly known as the Parasitica do not form a clade on their own 30 31 The common ancestor in which parasitoidism evolved lived approximately 247 million years ago and was previously believed to be an ectoparasitoid wood wasp that fed on wood boring beetle larvae Species similar in lifestyle and morphology to this ancestor still exist in the Ichneumonoidea 32 33 However recent molecular and morphological analysis suggests this ancestor was endophagous meaning it fed from within its host 30 A significant radiation of species in the Hymenoptera occurred shortly after the evolution of parasitoidy in the order and is thought to have been a result of it 31 33 The evolution of a wasp waist a constriction in the abdomen of the Apocrita contributed to rapid diversification as it increased maneuverability of the ovipositor the organ off the rear segment of the abdomen used to lay eggs 34 The phylogenetic tree gives a condensed overview of the positions of parasitoidal groups boldface amongst groups italics like the Vespidae which have secondarily abandoned the parasitoid habit The approximate numbers of species estimated to be in these groups often much larger than the number so far described is shown in parentheses with estimates for the most populous also shown in boldface like 150 000 Not all species in these groups are parasitoidal for example some Cynipoidea are phytophagous Hymenoptera Sawflies nbsp parasitoidism Orussoidea parasitoid wood wasps 85 nbsp Apocrita Ichneumonoidea 150 000 nbsp Cynipoidea 3 000 nbsp Proctotrupoidea 400 nbsp Platygastroidea 4000 nbsp Chalcidoidea 500 000 nbsp other SuperfamiliesAculeata Chrysididae jewel wasps 3000 nbsp Vespidae wasps hornets 5000 nbsp Mutillidae velvet ants 3000 nbsp Pompilidae spider wasps 5000 nbsp other familiesScoliidae 560 nbsp Formicidae ants 22 000 nbsp Apoidea Sphecidae 700 nbsp Bembicinae 1800 nbsp other familiesPemphredoninae aphid wasps 1000 nbsp Philanthinae 1100 nbsp Anthophila bees 22 000 nbsp stingingwasp waistevolved onceTaxonomy edit nbsp Trissolcus family Platygastridae on Chinavia eggs nbsp Housefly pupae killed by parasitoid wasp larvae probably Pteromalidae Each pupa has one hole through which a single adult wasp has emerged after feeding on the housefly larva The parasitoid wasps are paraphyletic since the ants bees and non parasitic wasps such as the Vespidae are not included and there are many members of mainly parasitoidal families which are not themselves parasitic Listed are Hymenopteran families where most members have a parasitoid lifestyle 35 Symphyta OrussidaeApocrita Scolebythidae Bethylidae Chrysididae Sclerogibbidae Dryinidae Embolemidae Tiphiidae Thynnidae Sapygidae Mutillidae Bradynobaenidae Chyphotidae Sierolomorphidae Braconidae Ichneumonidae Pompilidae Rhopalosomatidae Aulacidae Evaniidae Gasteruptiidae Stephanidae Megalyridae Trigonalidae Ibaliidae Liopteridae Figitidae Austroniidae Diapriidae Heloridae Monomachidae Pelecinidae Peradeniidae Proctotrupidae Roproniidae Vanhorniidae Platygastridae Scelionidae Megaspilidae Ceraphronidae Mymarommatidae Chalcidoidea 19 families AmpulicidaeInteractions with humans editBiological pest control edit nbsp Encarsia formosa an endoparasitic aphelinid wasp bred commercially to control whitefly in greenhouses nbsp Trioxys complanatus Aphidiinae ovipositing into a spotted alfalfa aphid a commercial pest in Australia a Further information Biological pest control Parasitoid wasps are considered beneficial as they naturally control the population of many pest insects They are widely used commercially alongside other parasitoids such as tachinid flies for biological pest control for which the most important groups are the ichneumonid wasps which prey mainly on caterpillars of butterflies and moths braconid wasps which attack caterpillars and a wide range of other insects including greenfly chalcidoid wasps which parasitise eggs and larvae of greenfly whitefly cabbage caterpillars and scale insects 37 One of the first parasitoid wasps to enter commercial use was Encarsia formosa an endoparasitic aphelinid It has been used to control whitefly in greenhouses since the 1920s Use of the insect fell almost to nothing replaced by chemical pesticides by the 1940s Since the 1970s usage has revived with renewed usage in Europe and Russia 38 In some countries such as New Zealand it is the primary biological control agent used to control greenhouse whiteflies particularly on crops such as tomato a particularly difficult plant for predators to establish on 39 Commercially there are two types of rearing systems short term seasonal daily output with high production of parasitoids per day and long term year round low daily output with a range in production of 4 1000 million female parasitoids per week to meet demand for suitable parasitoids for different crops 40 In culture edit Parasitoid wasps influenced the thinking of Charles Darwin b In an 1860 letter to the American naturalist Asa Gray Darwin wrote I cannot persuade myself that a beneficent and omnipotent God would have designedly created parasitic wasps with the express intention of their feeding within the living bodies of Caterpillars 3 The palaeontologist Donald Prothero notes that religiously minded people of the Victorian era including Darwin were horrified by this instance of evident cruelty in nature particularly noticeable in the Ichneumonidae 42 Notes edit Trioxys complanatus has been introduced to Australia to control the spotted alfalfa aphid 36 Darwin mentions parasitic wasps in On the Origin of Species Chapter 7 page 218 41 References edit Herniou Elisabeth A Huguet Elisabeth Theze Julien Bezier Annie Periquet Georges Drezen Jean Michel 2013 09 19 When parasitic wasps hijacked viruses genomic and functional evolution of polydnaviruses Phil Trans R Soc B 368 1626 20130051 doi 10 1098 rstb 2013 0051 PMC 3758193 PMID 23938758 Zhang Qi Kopylov Dmitry S Rasnitsyn Alexandr P Zheng Yan Zhang Haichun November 2020 Smith Andrew ed Burmorussidae a new family of parasitic wasps Insecta Hymenoptera from mid Cretaceous Burmese amber Papers in Palaeontology 6 4 593 603 doi 10 1002 spp2 1312 ISSN 2056 2802 S2CID 219039881 a b Letter 2814 Darwin C R to Gray Asa 22 May 1860 Retrieved 2011 04 05 a b Gullan P J Cranston P S 2010 The Insects An Outline of Entomology 5th ed Wiley pp 362 370 ISBN 978 1 118 84615 5 Cushman R A 1916 Syntomaspis druparum the apple seed chalcid Journal of Agricultural Research 7 487 502 Miller Lois K Ball Laurence Andrew 1998 The insect viruses Springer ISBN 978 0 306 45881 1 Strand Michael R Burke Gaelen R May 2015 Polydnaviruses From discovery to current insights Virology 479 480 393 402 doi 10 1016 j virol 2015 01 018 PMC 4424053 PMID 25670535 Cohen J E Jonsson T Muller C B Godfray H C J Savage V M 12 January 2005 Body sizes of hosts and parasitoids in individual feeding relationships Proceedings of the National Academy of Sciences 102 3 684 689 Bibcode 2005PNAS 102 684C doi 10 1073 pnas 0408780102 PMC 545575 PMID 15647346 nbsp Jones W Thomas 1982 Sex Ratio and Host Size in a Parasitoid Wasp Behavioral Ecology and Sociobiology 10 3 207 210 doi 10 1007 bf00299686 JSTOR 4599484 S2CID 28101144 Couchoux Christelle Seppa Perttu van Nouhuys Saskya 2015 Behavioural and genetic approaches to evaluate the effectiveness of deterrent marking by a parasitoid wasp Behaviour 152 9 1257 1276 doi 10 1163 1568539X 00003277 Nufio Cesar R Papaj Daniel R 2001 Host marking behavior in phytophagous insects and parasitoids Entomologia Experimentalis et Applicata 99 3 273 293 doi 10 1046 j 1570 7458 2001 00827 x nbsp Paladino Leonela Zusel Carabajal Papeschi Alba Graciela Cladera Jorge Luis January 2010 Immature stages of development in the parasitoid wasp Diachasmimorpha longicaudata Journal of Insect Science 10 1 56 doi 10 1673 031 010 5601 PMC 3014816 PMID 20569133 nbsp Cotesia congregata a parasitoid wasp entnemdept ufl edu Retrieved 2017 10 02 Jervis M A Kidd N A C November 1986 Host Feeding Strategies in Hymenopteran Parasitoids Biological Reviews 61 4 395 434 doi 10 1111 j 1469 185x 1986 tb00660 x S2CID 84430254 Fleming J G Summers M D 1991 Polydnavirus DNA is integrated in the DNA of its parasitoid wasp host PNAS 88 21 9770 9774 Bibcode 1991PNAS 88 9770F doi 10 1073 pnas 88 21 9770 PMC 52802 PMID 1946402 Webb Bruce A 1998 Polydnavirus Biology Genome Structure and Evolution In Miller L K Ball L A eds The Insect Viruses Springer Boston MA pp 105 139 doi 10 1007 978 1 4615 5341 0 5 ISBN 9781461374374 Roossinck M J 2011 Changes in population dynamics in mutualistic versus pathogenic viruses Viruses 3 12 12 19 doi 10 3390 v3010012 PMC 3187592 PMID 21994724 nbsp Strand M R Pech L L 1995 Immunological Basis for Compatibility in Parasitoid Host Relationships Annual Review of Entomology 40 31 56 doi 10 1146 annurev en 40 010195 000335 PMID 7810989 Gross P 1993 Insect Behavioral and Morphological defences Against Parasitoids Annual Review of Entomology 38 251 273 doi 10 1146 annurev en 38 010193 001343 Tanaka S Ohsaki N 2006 Behavioral manipulation of host caterpillars by the primary parasitoid wasp Cotesia glomerata L to construct defensive webs against hyperparasitism Ecological Research 21 4 570 doi 10 1007 s11284 006 0153 2 S2CID 23457678 Pennacchio Francesco Caccia Silvia Digilio Maria Cristina December 2014 Host regulation and nutritional exploitation by parasitic wasps Current Opinion in Insect Science 6 74 79 doi 10 1016 j cois 2014 09 018 ISSN 2214 5745 PMID 32846685 Oliver K M Russell J A Moran N A Hunter M S 2003 Facultative bacterial symbionts in aphids confer resistance to parasitic wasps Proceedings of the National Academy of Sciences 100 4 1803 7 Bibcode 2003PNAS 100 1803O doi 10 1073 pnas 0335320100 PMC 149914 PMID 12563031 Oliver K M Noge K Huang E M Campos J M Becerra J X Hunter M S 2012 Parasitic wasp responses to symbiont based defence in aphids BMC Biology 10 11 doi 10 1186 1741 7007 10 11 PMC 3312838 PMID 22364271 Singer M S Mace K C Bernays E A 2009 May Robin Charles ed Self Medication as Adaptive Plasticity Increased Ingestion of Plant Toxins by Parasitized Caterpillars PLOS ONE 4 3 e4796 Bibcode 2009PLoSO 4 4796S doi 10 1371 journal pone 0004796 PMC 2652102 PMID 19274098 Milan N F Kacsoh B Z Schlenke T A 2012 Alcohol Consumption as Self Medication against Blood Borne Parasites in the Fruit Fly Current Biology 22 6 488 493 doi 10 1016 j cub 2012 01 045 PMC 3311762 PMID 22342747 Kacsoh B Z Lynch Z R Mortimer N T Schlenke T A 2013 Fruit Flies Medicate Offspring After Seeing Parasites Science 339 6122 947 50 Bibcode 2013Sci 339 947K doi 10 1126 science 1229625 PMC 3760715 PMID 23430653 Branstetter Michael G Danforth Bryan N Pitts James P Faircloth Brant C Ward Philip S Buffington Matthew L Gates Michael W Kula Robert R Brady Sean G 2017 Phylogenomic Insights into the Evolution of Stinging Wasps and the Origins of Ants and Bees Current Biology 27 7 1019 1025 doi 10 1016 j cub 2017 03 027 PMID 28376325 nbsp Schulmeister S 2003 Simultaneous analysis of basal Hymenoptera Insecta introducing robust choice sensitivity analysis Biological Journal of the Linnean Society 79 2 245 275 doi 10 1046 j 1095 8312 2003 00233 x nbsp Schulmeister S Symphyta Retrieved 28 November 2016 a b c Peters Ralph S Krogmann Lars Mayer Christoph Donath Alexander Gunkel Simon Meusemann Karen Kozlov Alexey Podsiadlowski Lars Petersen Malte 2017 Evolutionary History of the Hymenoptera Current Biology 27 7 1013 1018 doi 10 1016 j cub 2017 01 027 hdl 2434 801122 PMID 28343967 a b Heraty John Ronquist Fredrik Carpenter James M Hawks David Schulmeister Susanne Dowling Ashley P Murray Debra Munro James Wheeler Ward C 2011 Evolution of the hymenopteran megaradiation PDF Molecular Phylogenetics and Evolution 60 1 73 88 doi 10 1016 j ympev 2011 04 003 PMID 21540117 Pennacchio Francesco Strand Michael R January 2006 Evolution of developmental strategies in parasitic hymenoptera Annual Review of Entomology 51 1 233 258 doi 10 1146 annurev ento 51 110104 151029 PMID 16332211 a b Whitfield James B 2003 Phylogenetic Insights into the Evolution of Parasitism in Hymenoptera Advances in Parasitology 54 69 100 doi 10 1016 S0065 308X 03 54002 7 ISBN 978 0 12 031754 7 PMID 14711084 Peters Ralph S Krogmann Lars Mayer Christoph Donath Alexander Gunkel Simon Meusemann Karen Kozlov Alexey Podsiadlowski Lars Petersen Malte April 2017 Evolutionary History of the Hymenoptera Current Biology 27 7 1013 1018 doi 10 1016 j cub 2017 01 027 hdl 2434 801122 ISSN 0960 9822 PMID 28343967 Henri Goulet Theodore Huber John T John Branch Canada Agriculture Canada Research 1993 Hymenoptera of the world an identification guide to families Centre for Land and Biological Resources Research ISBN 978 0660149332 OCLC 28024976 a href Template Cite book html title Template Cite book cite book a CS1 maint multiple names authors list link Wilson C G Swincer D E Walden K J 1982 The Introduction of Trioxys Complanatus Quilis Hymenoptera Aphidiidae an Internal Parasite of the Spotted Alfalfa Aphid into South Australia Australian Journal of Entomology 21 1 13 27 doi 10 1111 j 1440 6055 1982 tb01758 x Parasitoid Wasps Hymenoptera University of Maryland Retrieved 6 June 2016 Hoddle M S Van Driesche R G Sanderson J P 1998 Biology and Use of the Whitefly Parasitoid Encarsia Formosa Annual Review of Entomology 43 1 645 669 doi 10 1146 annurev ento 43 1 645 PMID 15012401 Enforce for Greenhouse Whitefly Control New Zealand Bioforce Limited Retrieved 26 January 2024 Smith S M 1996 Biological control with Trichogramma advances successes and potential of their use Annual Review of Entomology 41 375 406 doi 10 1146 annurev en 41 010196 002111 PMID 15012334 On the Origin of Species Chapter 7 page 218 Prothero Donald R 2017 Evolution What the Fossils Say and Why It Matters Columbia University Press pp 84 86 ISBN 978 0 231 54316 3 Retrieved from 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