Temporal range: 125–0Ma Middle Cretaceous - Recent
The Strepsiptera (translation: twisted wing, giving rise to the insects' common name, twisted-wing parasites) are an endopterygote order of insects with nine extant families making up about 600 species. The early-stage larvae and the short-lived adult males are non-sessile, but most of their lives are spent as endoparasites in other insects, such as bees, wasps, leafhoppers, silverfish, and cockroaches.
Appearance and biology
Males of the Strepsiptera have wings, legs, eyes, and antennae, and superficially look like flies, though their mouthparts cannot be used for feeding. Many of their mouthparts are modified into sensory structures. Adult males are very short-lived, usually surviving less than five hours, and do not feed. Females, in all families except the Mengenillidae, are not known to leave their hosts and are neotenic in form, lacking wings, legs, and eyes. Virgin females release a pheromone which the males use to locate them. In the Stylopidia, the female's anterior region protrudes out of the host body and the male mates by rupturing the female's brood canal opening, which lies between the head and prothorax. Sperm passes through the opening in a process termed hypodermic insemination. The offspring consume their mother from the inside in a process known as hemocelous viviparity. Each female thus produces many thousands of triungulin larvae that emerge from the brood opening on the head, which protrudes outside the host body. These larvae have legs (which lack a trochanter, the leg segment that forms the articulation between the basal coxa and the femur), and actively search out new hosts. Their hosts include members belonging to the orders Zygentoma, Orthoptera, Blattodea, Mantodea, Heteroptera, Hymenoptera, and Diptera. In the Strepsipteran family Myrmecolacidae, the males parasitize ants while the females parasitize Orthoptera.
|Suggested phylogenetic position of the
Strepsiptera eggs hatch inside the female, and the planidium larvae can move around freely within the female's haemocoel, which is unique to these animals. The female has a brood canal that communicates with the outside world, and the larvae escape through this. The larvae are very active, as they only have a limited amount of time to find a host before they exhaust their food reserves. These first-instar larvae have stemmata (simple, single-lens eyes), and once they latch onto a host, they enter it by secreting enzymes that soften the cuticle, usually in the abdominal region of the host. Some species have been reported to enter the eggs of hosts. Larvae of Stichotrema dallatorreanurn Hofeneder from Papua New Guinea were found to enter their orthopteran host's tarsus (foot). Once inside the host, they undergo hypermetamorphosis and become a less-mobile, legless larval form. They induce the host to produce a bag-like structure inside which they feed and grow. This structure, made from host tissue, protects them from the immune defences of the host. Larvae go through four more instars, and in each moult there is separation of the older cuticle but no discarding ("apolysis without ecdysis"), leading to multiple layers being formed around the larvae. Male larvae produce pupae after the last moult, but females directly become neotenous adults. The colour and shape of the host's abdomen may be changed and the host usually becomes sterile. The parasites then undergo pupation to become adults. Adult males emerge from the host bodies, while females stay inside. Females may occupy up to 90% of the abdominal volume of their hosts.
Adult male Strepsiptera have eyes unlike those of any other insect, resembling the schizochroal eyes found in the trilobite group known as Phacopida. Instead of a compound eye consisting of hundreds to thousands of ommatidia, each with a single lens and capable of producing a picture element (pixel), the strepsipteran eyes consist of only a few dozen "eyelets" that each produce a complete image. These eyelets are separated by cuticle and/or setae, giving the cluster eye as a whole a blackberry-like appearance.
Very rarely multiple females may live within a single stylopized host; multiple males within a single host are somewhat more common. Adult males are rarely observed, however, although specimens may be lured using cages containing virgin females. Nocturnal specimens can also be collected at light traps.
Strepsiptera may alter the behaviour of their hosts. Myrmecolacids may cause their ant hosts to climb up the tips of grass leaves, possibly to increase the spread of female pheromones to increase the chances of being located by males.
The order, named by William Kirby in 1813, is named for the hind wings (strepsi = twisted, ptera = wing), which are held at a twisted angle when at rest. The forewings are reduced to halteres (and initially were thought to be dried and twisted).
Strepsiptera are an enigma to taxonomists. Originally, they were believed to be the sister group to the beetle families Meloidae and Ripiphoridae, which have similar parasitic development and forewing reduction; early molecular research suggested their inclusion as a sister group to the flies, in a clade called the halteria, which have one pair of the wings modified into halteres, and failed to support their relationship to the beetles. More recent molecular studies, however, suggest they are outside the clade Mecopterida (containing the Diptera and Lepidoptera), yet there is no strong evidence for affinity with any other extant group. Study of their evolutionary position has been problematic due to difficulties in phylogenetic analysis arising from long branch attraction. The most basal strepsipteran is the fossil Protoxenos janzeni discovered in Baltic amber, while the most basal living strepsipteran is Bahiaxenos relictus, the sole member of the family Bahiaxenidae. The earliest known strepsipteran fossil is that of Cretostylops engeli, discovered in middle Cretaceous amber from Myanmar.
The Strepsiptera have two major groups: Stylopidia and Mengenillidia. The Mengenillidia include three extinct families (Cretostylopidae, Protoxenidae, and Mengeidae) plus two extant families (Bahiaxenidae and Mengenillidae; the latter is not monophyletic, however.) They are considered more primitive, and the known females (Mengenillidae only) are free-living, with rudimentary legs and antennae. The females have a single genital opening. The males have strong mandibles, a distinct labrum, and more than five antennal segments.
The other group, Stylopidia, includes seven families: Corioxenidae, Halictophagidae, Callipharixenidae, Bohartillidae, Elenchidae, Myrmecolacidae, and Stylopidae. All Stylopidia have endoparasitic females having multiple genital openings.
Stylopidae have four-segmented tarsi and four- to six-segmented antennae, with the third segment having a lateral process. The family Stylopidae may be paraphyletic. The Elenchidae have two-segmented tarsi and four-segmented antennae, with the third segment having a lateral process. The Halictophagidae have three-segmented tarsi and seven-segmented antennae, with lateral processes from the third and fourth segments. The Stylopidae mostly parasitize wasps and bees, the Elenchidae are known to parasitize Fulgoroidea, while the Halictophagidae are found on leafhoppers, treehoppers and mole cricket hosts.
Strepsipteran insects in the genus Xenos parasitize Polistes carnifex, a species of social wasps. These obligate parasites infect the developing wasp larvae in the nest and are present within the abdomens of female wasps when they hatch out. Here they remain until they thrust through the cuticle and pupate (males) or release infective first-instar larvae onto flowers (females). These larvae are transported back to their nests by foraging wasps.
- Whiting, M. F (2003). "Strepsiptera". In Resh, V. H. & R. T. Cardé. Encyclopedia of Insects. Academic Press. pp. 1094–1096.
- Borror, D.J., Triplehorn, C.A. Johnson (1989). Introduction to the Study of Insects (6 ed.). Brooks Cole.
- Kathirithamby, Jeyaraney. 2002. Strepsiptera. Twisted-wing parasites. Version 24 September 2002.  in The Tree of Life Web Project
- Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
- Kathirithamby, Jeyaraney (2001). "Stand Tall and They Still Get You in Your Achilles Foot-Pad". Proceedings: Biological Sciences 268 (1483): 2287–2289. doi:10.1098/rspb.2001.1810.
- Kathirithamby, Jeyaraney; Ross, Larry D.; Johnston, J. Spencer (2003). "Masquerading as Self? Endoparasitic Strepsiptera (Insecta) Enclose Themselves in Host-Derived Epidermal Bag". Proceedings of the National Academy of Sciences of the United States of America 100 (13): 7655–7659. doi:10.1073/pnas.1131999100.
- Beani, Laura (2006). "Crazy wasps: when parasites manipulate the Polistes phenotype" (PDF). Ann. Zool. Fennici 43: 564–574.
- Kathirithamby, J (2000). "Morphology of the female Myrmecolacidae (Strepsiptera) including the apron, and an associated structure analogous to the peritrophic matrix". Zoological Journal of the Linnean Society 128: 269–287. doi:10.1111/j.1096-3642.2000.tb00164.x.
- Buschbeck,E. K.,B. Ehmer, R. R. Hoy (2003). "The unusual visual system of the Strepsiptera: external eye and neuropils" (PDF). J. Comp. Physiol. A 189: 617–630. doi:10.1007/s00359-003-0443-x.
- Wojcik, Daniel P. (1989) Behavioral Interactions between Ants and Their Parasites. The Florida Entomologist. 72(1):43-51.
- Whiting, Michael F. (1998). "Long-Branch Distraction and the Strepsiptera" (PDF). Systematic Biology 47 (1): 134–138. doi:10.1080/106351598261076.
- Whiting, Michael F.; Carpenter, James C.; Wheeler, Quentin D.; Wheeler, Ward C. (1997). "The Stresiptera Problem: Phylogeny of the Holometabolous Insect Orders Inferred from 18S and 28S Ribosomal DNA Sequences and Morphology". Systematic Biology 46 (1): 1–68. doi:10.2307/2413635.
- Bonneton, F.; Brunet, F. G.; Kathirithamby, J.; Laudet, V. (2006). "The rapid divergence of the ecdysone receptor is a synapomorphy for Mecopterida that clarifies the Strepsiptera problem". Insect Molecular Biology 15 (3): 351–362. doi:10.1111/j.1365-2583.2006.00654.x.
- Huelsenbeck, John P (1998). "Systematic Bias in Phylogenetic Analysis: Is the Strepsiptera Problem Solved?". Systematic Biology 47 (3): 519–537.
- Pohl, H.; Beutel, R.G.; Kinzelbach, R. (2005). "Protoxenidae fam. nov. (Insecta, Strepsiptera) from Baltic amber—a 'missing link' in strepsipteran phylogeny". Zool. Scr 34: 57–69. doi:10.1111/j.1463-6409.2005.00173.x.
- Bravo, Pohl; Silva-Neto; Beutel (2009). "Bahiaxenidae, a "living fossil" and a new family of Strepsiptera (Hexapoda) discovered in Brazil". Cladistics 25: 614–623. doi:10.1111/j.1096-0031.2009.00264.x.
- Grimaldi, D.; Kathirithamby, J.; Schawaroch, V. (2005). "Strepsiptera and triungula in Cretaceous amber". Insect Syst. Evol 36: 1–20. doi:10.1163/187631205788912787.
- Niehuis O, Hartig G, Grath S, Pohl H, Lehmann J, Tafer H, Donath A, Krauss V, Eisenhardt C, Hertel J, Petersen M, Mayer C, Meusemann K, Peters RS, Stadler PF, Beutel RG, Bornberg-Bauer E, McKenna DD, Misof B (2012) Genomic and Morphological Evidence Converge to Resolve the Enigma of Strepsiptera. Curr Biol
- Kathirithamby, Jeyaraney; Hughes, David (2006). "Description and biological notes of the first species of Xenos (Strepsiptera: Stylopidae) parasitic in Polistes carnifex F. (Hymenoptera: Vespidae) in Mexico". Zootaxa 1104: 35–45.
- Hughes, D. P.; Beani, L.; Turillazzi, S.; Kathirithamby, J. (2003). "Prevalence of the parasite Strepsiptera in Polistes as detected by dissection of immatures". Insectes Sociaux 50 (1): 62–68. doi:10.1007/s000400300010.
- Grimaldi, D. and Engel, M.S. (2005). Evolution of the Insects. Cambridge University Press. ISBN 0-521-82149-5.
|Wikimedia Commons has media related to Strepsiptera.|
|Wikispecies has information related to: Strepsiptera|
- Strepsiptera in Baltic amber (www.amber-inclusions.dk) - Strepsiptera, Mengeidae, Mengea tertiaria
- Survey of Modern Counterparts of Schizochroal Trilobite Eyes: Structural and Functional Similarities and Differences
- Family outline: Strepsiptera