Ichneumonoidea

The superfamily Ichneumonoidea contains one extinct and three extant families, including the two largest families within Hymenoptera: Ichneumonidae and Braconidae. The group is thought to contain as many as 100,000 species, many of which have not yet been described.[1] Like other parasitoid wasps, they were long placed in the "Parasitica", variously considered as an infraorder or an unranked clade, now known to be paraphyletic.

Ichneumonoidea
Temporal range: Cretaceous-Present
Megarhyssa greenei female
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Suborder: Apocrita
Superfamily: Ichneumonoidea
Latreille, 1802
Families

Etymology

The name is derived from Latin 'ichneumon', from Ancient Greek ἰχνεύμων (ikhneúmōn, "tracker"), from ἴχνος (íkhnos, "track, footstep"). The name is shared with the Egyptian mongoose, Herpestes ichneumon.

Description

The superfamily is defined by fusion of the costal and radial veins of the fore wing, and almost all species have more than 11 antennal segments.[2] Both included families have a cosmopolitan distribution. Ichneumonoids have morphological similarities with relatives within the order Hymenoptera, including ants and bees. Ichneumonoidea contains a great deal of morphological diversity, with species ranging in size from 3 to 130 mm (0.12 to 5.12 in) long. Most are slender, and the females of many species (particularly in the genus Megarhyssa) have extremely long ovipositors for laying eggs.

The ichneumonid wasps may be more familiar to non-entomologists than braconids, as they are generally larger. The two families are distinguished from each other primarily by details of wing venation.

Braconidae

Most are brownish or black, not brightly colored.[3] Fore wings lack vein 2m-cu.

Ichneumonidae

Ichneumonids vary greatly in size and their color varies from brightly colored yellow to uniform black. Fore wing with vein 2m-cu present and tubular.[2]

Trachypetidae

The family Trachypetidae was erected in 2020 for three Australian genera formerly included in the Braconidae.[4]

Evolution

Parasitoidism evolved only once in the Hymenoptera, during the Permian, leading to a single clade, the Apocrita. The Apocrita emerged during the Jurassic.[5][6][7][8]

Hymenoptera

Sawflies

Orussoidea

Apocrita
Ichneumonoidea

Ichneumonidae

Braconidae

Trachypetidae

Chalcidoidea and allies

Aculeata

 wasp waist 
 parasitoidism 

Parasitic life cycle

Ichneumonoids are solitary insects, and the vast majority are parasitoids; the larvae feed on or in another insect until it finally dies. Most hosts are holometabolus insect larvae, but there are many exceptions. In general, ichneumonoids are host specific, and only attack one or a few closely related host species. Many species use polydnaviruses to suppress the immune systems of their host insects. Due to the wide variety in hosts and lifestyles, see subfamily pages for more detail.

The female ichneumonoid finds a host and lays an egg on, near, or inside the host's body.[9] The ovipositor of ichneumonoids generally cannot deliver a sting as many wasps or bees do. It can be used to bore wood and lay eggs on hosts deep inside, or reach hosts hidden inside leaf shelters. Upon hatching, the larva feeds either externally or internally, killing the host when it is ready to pupate.

Various ichneumonoids are used as biological control agents in controlling horticultural or forest pests. An example is the relationship between the species Ichneumon eumerus and its host butterfly Phengaris rebeli.[10] The butterfly larva is a parasite within Myrmica ant nests. The adult I. eumerus searches for ant nests and only enters when they contain P. rebeli caterpillars.[10] Once inside, they oviposit within the caterpillars and escape the nest by releasing a chemical which causes the worker ants to fight each other rather than the intruding wasp.[10] The wasp eggs then hatch inside the caterpillar and eventually consume and kill the host.

Life cycle of Hercus fontinalis

References

  1. Pennacchio, Francesco; Strand, Michael R. (2005-12-06). "Evolution of developmental strategies in parasitic hymenoptera". Annual Review of Entomology. 51 (1): 233–258. doi:10.1146/annurev.ento.51.110104.151029. ISSN 0066-4170. PMID 16332211.
  2. H., Goulet; J.T., Huber (1993). "10: Superfamily Ichneumonoidea". Hymenoptera of the world: An identification guide to families.
  3. Borror and White
  4. D.L.J. Quicke, A.D. Austin, E.P. Fagan‐Jeffries. P.D.N. Hebert, B.A. Butcher (2020) Recognition of the Trachypetidae stat.n. as a new extant family of Ichneumonoidea (Hymenoptera), based on molecular and morphological evidence. Systematic Entomology. DOI: 10.1111/syen.12426
  5. 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.
  6. 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.
  7. Schulmeister, S. "Symphyta". Retrieved 28 November 2016.
  8. 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. PMID 28343967.
  9. Sezen, Uzay. "Two ichneumon wasps competing to oviposit". Retrieved 12 September 2011.
  10. Hochberg, M; Elmes, G. W.; Thomas, J. A.; Clarke, R. T (1996). "Mechanisms of local persistence in coupled host-parasitoid associations: the case model of Maculinea rebeli and Ichneumon eumerus". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 351 (1348): 1713–1724. Bibcode:1996RSPTB.351.1713H. doi:10.1098/rstb.1996.0153.
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